EP1045893A2 - Moulded body dishwasher detergents containing surfactants - Google Patents
Moulded body dishwasher detergents containing surfactantsInfo
- Publication number
- EP1045893A2 EP1045893A2 EP98966386A EP98966386A EP1045893A2 EP 1045893 A2 EP1045893 A2 EP 1045893A2 EP 98966386 A EP98966386 A EP 98966386A EP 98966386 A EP98966386 A EP 98966386A EP 1045893 A2 EP1045893 A2 EP 1045893A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- component
- molded body
- body according
- group
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
- 239000004094 surface-active agent Substances 0.000 title claims abstract description 33
- 239000003599 detergent Substances 0.000 title claims description 19
- 239000004615 ingredient Substances 0.000 claims abstract description 57
- 239000007844 bleaching agent Substances 0.000 claims abstract description 31
- 239000000126 substance Substances 0.000 claims abstract description 24
- 108090000790 Enzymes Proteins 0.000 claims abstract description 15
- 102000004190 Enzymes Human genes 0.000 claims abstract description 15
- 239000003513 alkali Substances 0.000 claims abstract description 8
- 239000013543 active substance Substances 0.000 claims abstract description 7
- 239000000969 carrier Substances 0.000 claims abstract description 4
- 239000000203 mixture Substances 0.000 claims description 65
- 239000001993 wax Substances 0.000 claims description 41
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 25
- 150000002170 ethers Chemical class 0.000 claims description 23
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 21
- -1 n- Nonanoyl Chemical group 0.000 claims description 21
- 239000003795 chemical substances by application Substances 0.000 claims description 18
- 229910017052 cobalt Inorganic materials 0.000 claims description 17
- 239000010941 cobalt Substances 0.000 claims description 17
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 17
- 239000012190 activator Substances 0.000 claims description 16
- 239000002736 nonionic surfactant Substances 0.000 claims description 15
- 150000001875 compounds Chemical class 0.000 claims description 14
- 150000002191 fatty alcohols Chemical class 0.000 claims description 14
- 238000004851 dishwashing Methods 0.000 claims description 13
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 12
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 12
- 229920002678 cellulose Polymers 0.000 claims description 12
- 235000010980 cellulose Nutrition 0.000 claims description 12
- 229910052709 silver Inorganic materials 0.000 claims description 12
- 239000004332 silver Substances 0.000 claims description 12
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- 239000002253 acid Substances 0.000 claims description 9
- 150000007513 acids Chemical class 0.000 claims description 9
- 229910052748 manganese Inorganic materials 0.000 claims description 9
- 239000011572 manganese Substances 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 229910052723 transition metal Inorganic materials 0.000 claims description 8
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 7
- 229920001577 copolymer Polymers 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 7
- 239000002689 soil Substances 0.000 claims description 7
- ZGZHWIAQICBGKN-UHFFFAOYSA-N 1-nonanoylpyrrolidine-2,5-dione Chemical compound CCCCCCCCC(=O)N1C(=O)CCC1=O ZGZHWIAQICBGKN-UHFFFAOYSA-N 0.000 claims description 6
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims description 6
- 150000001868 cobalt Chemical class 0.000 claims description 6
- 238000005260 corrosion Methods 0.000 claims description 6
- 230000007797 corrosion Effects 0.000 claims description 6
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 6
- 229920001223 polyethylene glycol Polymers 0.000 claims description 6
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 6
- 235000017550 sodium carbonate Nutrition 0.000 claims description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
- 238000004061 bleaching Methods 0.000 claims description 5
- 239000000460 chlorine Substances 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 5
- 235000019832 sodium triphosphate Nutrition 0.000 claims description 5
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 claims description 5
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 4
- 150000001805 chlorine compounds Chemical class 0.000 claims description 4
- QAHREYKOYSIQPH-UHFFFAOYSA-L cobalt(II) acetate Chemical class [Co+2].CC([O-])=O.CC([O-])=O QAHREYKOYSIQPH-UHFFFAOYSA-L 0.000 claims description 4
- 229940099596 manganese sulfate Drugs 0.000 claims description 4
- 239000011702 manganese sulphate Substances 0.000 claims description 4
- 235000007079 manganese sulphate Nutrition 0.000 claims description 4
- SQQMAOCOWKFBNP-UHFFFAOYSA-L manganese(II) sulfate Chemical compound [Mn+2].[O-]S([O-])(=O)=O SQQMAOCOWKFBNP-UHFFFAOYSA-L 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 150000004760 silicates Chemical class 0.000 claims description 4
- OCUCCJIRFHNWBP-IYEMJOQQSA-L Copper gluconate Chemical class [Cu+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O OCUCCJIRFHNWBP-IYEMJOQQSA-L 0.000 claims description 3
- 125000005263 alkylenediamine group Polymers 0.000 claims description 3
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 3
- 238000005336 cracking Methods 0.000 claims description 3
- 238000005187 foaming Methods 0.000 claims description 3
- 150000004967 organic peroxy acids Chemical class 0.000 claims description 3
- 239000002304 perfume Substances 0.000 claims description 3
- PATMLLNMTPIUSY-UHFFFAOYSA-N phenoxysulfonyl 7-methyloctanoate Chemical compound CC(C)CCCCCC(=O)OS(=O)(=O)OC1=CC=CC=C1 PATMLLNMTPIUSY-UHFFFAOYSA-N 0.000 claims description 3
- 229910000030 sodium bicarbonate Inorganic materials 0.000 claims description 3
- 235000017557 sodium bicarbonate Nutrition 0.000 claims description 3
- 239000004705 High-molecular-weight polyethylene Substances 0.000 claims description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- 150000001412 amines Chemical class 0.000 claims description 2
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims description 2
- 239000012964 benzotriazole Substances 0.000 claims description 2
- 150000001565 benzotriazoles Chemical class 0.000 claims description 2
- 239000002360 explosive Substances 0.000 claims description 2
- PMYUVOOOQDGQNW-UHFFFAOYSA-N hexasodium;trioxido(trioxidosilyloxy)silane Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[O-][Si]([O-])([O-])O[Si]([O-])([O-])[O-] PMYUVOOOQDGQNW-UHFFFAOYSA-N 0.000 claims description 2
- 229920001519 homopolymer Polymers 0.000 claims description 2
- 150000007524 organic acids Chemical class 0.000 claims description 2
- 235000005985 organic acids Nutrition 0.000 claims description 2
- YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 claims description 2
- 235000021317 phosphate Nutrition 0.000 claims description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 2
- 239000003223 protective agent Substances 0.000 claims description 2
- 239000001509 sodium citrate Substances 0.000 claims description 2
- 235000012207 sodium gluconate Nutrition 0.000 claims description 2
- 150000003852 triazoles Chemical class 0.000 claims description 2
- HRXKRNGNAMMEHJ-UHFFFAOYSA-K trisodium citrate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O HRXKRNGNAMMEHJ-UHFFFAOYSA-K 0.000 claims description 2
- 229940038773 trisodium citrate Drugs 0.000 claims description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims 2
- FRPJTGXMTIIFIT-UHFFFAOYSA-N tetraacetylethylenediamine Chemical compound CC(=O)C(N)(C(C)=O)C(N)(C(C)=O)C(C)=O FRPJTGXMTIIFIT-UHFFFAOYSA-N 0.000 claims 2
- 238000003860 storage Methods 0.000 abstract description 7
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- 239000007884 disintegrant Substances 0.000 description 16
- 238000009472 formulation Methods 0.000 description 16
- 150000001298 alcohols Chemical class 0.000 description 12
- 238000004140 cleaning Methods 0.000 description 12
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 11
- 229940088598 enzyme Drugs 0.000 description 11
- 235000019271 petrolatum Nutrition 0.000 description 11
- 239000012459 cleaning agent Substances 0.000 description 10
- 230000000694 effects Effects 0.000 description 10
- 238000000465 moulding Methods 0.000 description 10
- 235000019809 paraffin wax Nutrition 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 239000011248 coating agent Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 8
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- 229910052742 iron Inorganic materials 0.000 description 6
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- BGRWYDHXPHLNKA-UHFFFAOYSA-N Tetraacetylethylenediamine Chemical compound CC(=O)N(C(C)=O)CCN(C(C)=O)C(C)=O BGRWYDHXPHLNKA-UHFFFAOYSA-N 0.000 description 5
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- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
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- 229920002472 Starch Polymers 0.000 description 4
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 4
- UAOKXEHOENRFMP-ZJIFWQFVSA-N [(2r,3r,4s,5r)-2,3,4,5-tetraacetyloxy-6-oxohexyl] acetate Chemical compound CC(=O)OC[C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](OC(C)=O)C=O UAOKXEHOENRFMP-ZJIFWQFVSA-N 0.000 description 4
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- QLIBJPGWWSHWBF-UHFFFAOYSA-N 2-aminoethyl methacrylate Chemical compound CC(=C)C(=O)OCCN QLIBJPGWWSHWBF-UHFFFAOYSA-N 0.000 description 1
- JSIAIROWMJGMQZ-UHFFFAOYSA-N 2h-triazol-4-amine Chemical class NC1=CNN=N1 JSIAIROWMJGMQZ-UHFFFAOYSA-N 0.000 description 1
- YNJSNEKCXVFDKW-UHFFFAOYSA-N 3-(5-amino-1h-indol-3-yl)-2-azaniumylpropanoate Chemical class C1=C(N)C=C2C(CC(N)C(O)=O)=CNC2=C1 YNJSNEKCXVFDKW-UHFFFAOYSA-N 0.000 description 1
- AACHVWXCVWWMSI-UHFFFAOYSA-N 3-hydroxypropyl(trimethyl)azanium Chemical compound C[N+](C)(C)CCCO AACHVWXCVWWMSI-UHFFFAOYSA-N 0.000 description 1
- UZJGVXSQDRSSHU-UHFFFAOYSA-N 6-(1,3-dioxoisoindol-2-yl)hexaneperoxoic acid Chemical compound C1=CC=C2C(=O)N(CCCCCC(=O)OO)C(=O)C2=C1 UZJGVXSQDRSSHU-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical group C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
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- 241001440269 Cutina Species 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- PHOQVHQSTUBQQK-SQOUGZDYSA-N D-glucono-1,5-lactone Chemical compound OC[C@H]1OC(=O)[C@H](O)[C@@H](O)[C@@H]1O PHOQVHQSTUBQQK-SQOUGZDYSA-N 0.000 description 1
- 229920002307 Dextran Polymers 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
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- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- 240000007049 Juglans regia Species 0.000 description 1
- 235000009496 Juglans regia Nutrition 0.000 description 1
- 241001148717 Lygeum spartum Species 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
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- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 239000004264 Petrolatum Substances 0.000 description 1
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- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920002565 Polyethylene Glycol 400 Polymers 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 244000044822 Simmondsia californica Species 0.000 description 1
- 235000004433 Simmondsia californica Nutrition 0.000 description 1
- XYQRXRFVKUPBQN-UHFFFAOYSA-L Sodium carbonate decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].[O-]C([O-])=O XYQRXRFVKUPBQN-UHFFFAOYSA-L 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
- 150000008041 alkali metal carbonates Chemical class 0.000 description 1
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- 150000008064 anhydrides Chemical class 0.000 description 1
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- 125000004429 atom Chemical group 0.000 description 1
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- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 108010064866 biozym Proteins 0.000 description 1
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- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 238000005056 compaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- GQOKIYDTHHZSCJ-UHFFFAOYSA-M dimethyl-bis(prop-2-enyl)azanium;chloride Chemical compound [Cl-].C=CC[N+](C)(C)CC=C GQOKIYDTHHZSCJ-UHFFFAOYSA-M 0.000 description 1
- 235000021186 dishes Nutrition 0.000 description 1
- VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000004049 embossing Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000006266 etherification reaction Methods 0.000 description 1
- 238000007046 ethoxylation reaction Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 235000012209 glucono delta-lactone Nutrition 0.000 description 1
- 229960003681 gluconolactone Drugs 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 125000001046 glycoluril group Chemical group [H]C12N(*)C(=O)N(*)C1([H])N(*)C(=O)N2* 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 229910052735 hafnium Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 125000001841 imino group Chemical group [H]N=* 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- VYFOAVADNIHPTR-UHFFFAOYSA-N isatoic anhydride Chemical compound NC1=CC=CC=C1CO VYFOAVADNIHPTR-UHFFFAOYSA-N 0.000 description 1
- 239000012182 japan wax Substances 0.000 description 1
- 150000003951 lactams Chemical class 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 150000002646 long chain fatty acid esters Chemical class 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 150000002696 manganese Chemical class 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 108010003855 mesentericopeptidase Proteins 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 108010020132 microbial serine proteinases Proteins 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 239000012184 mineral wax Substances 0.000 description 1
- 239000012170 montan wax Substances 0.000 description 1
- 238000006384 oligomerization reaction Methods 0.000 description 1
- 239000012168 ouricury wax Substances 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 150000004965 peroxy acids Chemical class 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 1
- 229960001553 phloroglucinol Drugs 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000223 polyglycerol Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 229920001592 potato starch Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 238000006268 reductive amination reaction Methods 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 150000003334 secondary amides Chemical class 0.000 description 1
- 239000011257 shell material Substances 0.000 description 1
- 239000012176 shellac wax Substances 0.000 description 1
- 238000005029 sieve analysis Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229940018038 sodium carbonate decahydrate Drugs 0.000 description 1
- 229960001922 sodium perborate Drugs 0.000 description 1
- 229940045872 sodium percarbonate Drugs 0.000 description 1
- 229910000031 sodium sesquicarbonate Inorganic materials 0.000 description 1
- 235000018341 sodium sesquicarbonate Nutrition 0.000 description 1
- MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 235000013616 tea Nutrition 0.000 description 1
- 150000004685 tetrahydrates Chemical class 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000003623 transition metal compounds Chemical class 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- WCTAGTRAWPDFQO-UHFFFAOYSA-K trisodium;hydrogen carbonate;carbonate Chemical compound [Na+].[Na+].[Na+].OC([O-])=O.[O-]C([O-])=O WCTAGTRAWPDFQO-UHFFFAOYSA-K 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 239000012178 vegetable wax Substances 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 238000004018 waxing Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 150000003752 zinc compounds Chemical class 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical class [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0047—Detergents in the form of bars or tablets
- C11D17/0065—Solid detergents containing builders
- C11D17/0073—Tablets
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0047—Detergents in the form of bars or tablets
- C11D17/0065—Solid detergents containing builders
- C11D17/0073—Tablets
- C11D17/0091—Dishwashing tablets
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/06—Phosphates, including polyphosphates
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/26—Organic compounds containing nitrogen
- C11D3/28—Heterocyclic compounds containing nitrogen in the ring
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/395—Bleaching agents
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3902—Organic or inorganic per-compounds combined with specific additives
- C11D3/3905—Bleach activators or bleach catalysts
- C11D3/3907—Organic compounds
- C11D3/3915—Sulfur-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3902—Organic or inorganic per-compounds combined with specific additives
- C11D3/3905—Bleach activators or bleach catalysts
- C11D3/3907—Organic compounds
- C11D3/3917—Nitrogen-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3902—Organic or inorganic per-compounds combined with specific additives
- C11D3/3905—Bleach activators or bleach catalysts
- C11D3/3932—Inorganic compounds or complexes
Definitions
- the invention relates to washing or cleaning active moldings, primarily tablets such as dishwasher tablets, detergent tablets, bleach tablets, stain remover tablets or water softening tablets for use in the home, in particular for mechanical use, and a process for producing these moldings and their use.
- tablets such as dishwasher tablets, detergent tablets, bleach tablets, stain remover tablets or water softening tablets for use in the home, in particular for mechanical use, and a process for producing these moldings and their use.
- Shaped or active cleaning moldings in particular tablets, have a number of advantages over powder-form agents, such as advantageous handling, simple dosing and low packaging volume requirements.
- the application therefore relates to a molded article containing builder substances, alkali carriers, bleaches and enzymes, characterized in that in an area not greater than 40% by volume, more than 80% by weight, of an active substance (I) with a constituent from the Group of surfactants is included.
- the ingredient (I) can also contain at least one bleach from the group of chlorine and / or oxygen lead agents, a bleach activator, a silver protection agent and / or a soil release compound, an enzyme or a component or a compound for solubility control contain.
- the ingredient (I) can also be a mixture of several of these ingredients.
- the ingredient (I) is a mixture of a component or a compound for solubility control, a surfactant and at least one other ingredient from the group consisting of bleaching agent and / or bleach activator and / or silver protective agent and / or soil release - Compound and / or enzyme and / or a surfactant.
- the solubility of the area with the ingredient (I), the surface and the type of compression and the storage stability can also have a decisive influence on the properties of the tablet.
- the range contains more than 80% by weight, preferably more than 90% by weight, particularly preferably more than 95% by weight, very particularly preferably the total amount of an ingredient (I) present in exactly three spatial directions is surrounded by other ingredients of the molded body.
- a desirable influence on the overall result can also be achieved if the weight increase of the area containing more than 80% by weight of the content (I) when stored under normal household conditions, i. H. between 15 and 30 ° C and between 5 and 55% atmospheric humidity, preferably 15 and 35% atmospheric humidity for a period of 30 days, preferably 60 days, particularly preferably 90 days, not more than 50% by weight, preferably not more than 40% %, very particularly preferably not more than 30% by weight, extremely preferably not more than 20% by weight and extremely preferably not more than 10% by weight, at best not more than 5% by weight.
- a desirable influence on the overall result can also be achieved if the loss of .active substance (I) in the region containing more than 80% by weight of an ingredient when stored under normal household conditions, i. H. between 15 and 30 ° C. and between 5 and 55% atmospheric humidity, preferably 15 and 35% atmospheric humidity for a period of 30 days, preferably 60 days, particularly preferably 90 days, not more than 50% by weight, preferably not more than 40% %, very particularly preferably not more than 30% by weight, extremely preferably not more than 20% by weight and extremely preferably not more than 10% by weight, at best not more than 5% by weight.
- a desirable influence on the overall result can also be achieved if the absorption maximum of a 1% solution of a colored area or a colored component when stored under normal household conditions, ie between 15 and 30 ° C. and between 5 and 55% atmospheric humidity, preferably 15 and 35% humidity for a period of 30 days, preferably 60 days, particularly preferably 90 days, not more than 100 wave numbers, preferably not more than 50 wave numbers, very particularly preferably not more than 30 wave numbers, extremely preferably not melir than 20 wavenumbers and most preferably not more than 10 wavenumbers, at best not more than 5 wavenumbers.
- the molded body according to the invention also has a positive effect if the region with more than 80% by weight, preferably more than 90% by weight, particularly preferably more than 95% by weight, very particularly preferably the total amount of an ingredient present ( I) is surrounded by other ingredients of the molded body in exactly three spatial directions.
- the solubility can be influenced by components and / or compounds to accelerate solubility (disintegrant) or to delay solubility.
- disintegrants known in the prior art can be used as disintegrants. Particular reference is made to the textbooks Rompp (9th edition, vol. 6, p. 4440) and Voigt "Textbook of pharmaceutical technology” (6th edition, 1987). Substances such as starch, cellulose and cellulose derivatives, alginates, Dextrans, cross-linked polyvinylpyrrolidones and others; systems of weak acids and carbonate-containing agents, in particular citric acid and tartaric acid in combination with bicarbonate or carbonate as well as polyethylene glycol sorbitan fatty acid esters.
- German patent application DE 938 566 it is proposed to convert acetylsalicylic acid into granular form before pressing, to dry it gently but completely and then to coat it with highly disperse silica. Subsequently, the acetylsalicylic acid granules powdered with finely divided silica can be mixed with other tablet ingredients, which may be in powder or granular form, and pressed into tablets.
- the separating layer of highly disperse silica not only acts as an insulating layer and protection against unwanted reactions, but also contributes to the rapid disintegration of the tablets even after a long storage period.
- German patent application DE 12 28 029 describes the production of tablets, powder mixtures without prior granulation initially containing cellulose powder and mixed if necessary, highly disperse silica, mixed according to a preferred embodiment and then pressed.
- German patent application DE 41 21 127 again shows that a particularly good auxiliary in the manufacture of pharmaceutical tablets has cellulose particles on the surface of which a laminating agent is fixed.
- the excipient is used in the finest possible form; mean particle sizes below 200 ⁇ m are shown to be particularly advantageous.
- the classic tablet disintegrants of the first class of substances mentioned are mixed in very fine-particle form either before being compressed with the other tablet ingredients, which may be in fine or granular form, or the other tablet ingredients are coated or powdered with the tablet disintegrant.
- disintegrants which are known from the manufacture of pharmaceuticals. Swelling layer silicates such as bentonites, natural substances and natural substance derivatives based on starch and cellulose, alginates and the like, potato starch, methyl cellulose and / or hydroxypropyl cellulose are mentioned as disintegrants. These disintegrants can be mixed with the granules to be milled, but can also be incorporated into the granules to be milled.
- EP-A-0 466485, EP-A-0 522 766, EP-A-0 711 827, EP-A-0 711 828 and EP-A-0 716 144 describe the production of active cleaning tablets, using compact, particulate material with a particle size between 180 and 2000 ⁇ m.
- the resulting tablets can both have a homogeneous as well as a heterogeneous structure.
- EP-A-0 522 766 at least the particles which contain surfactants and builders are coated with a solution or dispersion of a binder / disintegrant, in particular polyethylene glycol.
- binders / disintegrants are again the disintegrants already described and known, for example starches and starch derivatives, commercially available cellulose derivatives such as crosslinked and modified cellulose, microcrystalline cellulose fibers, crosslinked polyvinylpyrrolidones, layered silicates etc.
- weak acids such as citric acid or tartaric acid or tartaric acid or tartaric acid which, in connection with carbonate-containing sources, lead to sprinkling effects when in contact with water and which, according to Römpp's definition, belong to the second class of disintegrants, can be used as a coating material.
- disintegrants whose particle size distribution (sieve analysis) is designed in such a way that a maximum of 1% by weight, preferably less, of dust components is present and overall (including any dust components present) less than 10% by weight of the disintegrant granules are smaller than 0.2 mm. At least 90% by weight of the disintegrant granules advantageously have a particle size of at least 0.2 mm and a maximum of 3 mm. These disintegrants are particularly suitable for the present invention.
- the dissolution time of the entire molded article is preferably shorter than the duration of the main wash cycle of a conventional dishwasher, i.e. shorter than 40 min, particularly preferably shorter than 30 min, very particularly preferably shorter than 20 min and extremely preferably shorter than 10 min.
- Paraffins and / or microwaxes and / or the high molecular weight polyethylene glycols which are described in detail in the prior art, are generally used as the material for delaying dissolution.
- the use of mixtures as mentioned in the unpublished publication DE 197 27 073 and the disclosure of which is hereby expressly incorporated into this document is particularly suitable for the present application. If a component for delaying dissolution is included, the dissolution time of the entire molded body in 20 ° C. cold water is longer in a preferred embodiment than the pre-rinse cycle of a commercially available dishwasher, that is to say longer than 5 minutes, preferably longer than 10 minutes.
- homogeneous or heterogeneous molded bodies of known design are provided.
- These include in particular cylindrical tablets, these tablets preferably having a diameter of 15 to 60 mm, in particular 30 +/- 10 mm.
- the height of these tablets is preferably 5 to 30 mm and in particular 15 to 28 mm.
- Shaped bodies with a diameter of 32, 33, 34, 35, 36, 37, 38 and 39 mm have proven to be particularly favorable. In special designs, the height is 24, 25, 26, 27 or 28 mm.
- the edge lengths are preferably between 15 to 60 mm, in particular 30 +/- 10 mm.
- the weight of the individual shaped bodies, in particular the tablets, is preferably 15 to 60 g and in particular 20 to 40 g per shaped body or tablet; the consistency of the molded body or tablets, however, usually has values above 1 kg / dm, preferably from 1.1 to 1.4 kg / dm.
- the water hardness range or the level of contamination 1 or more, for example 2 to 4, molded articles, in particular tablets, can be used.
- the Further shaped bodies according to the invention can also have smaller diameters or dimensions, for example around 10 mm.
- a homogeneous shaped body is understood to mean those in which the ingredients of the fora body are homogeneously distributed except for the area with ingredient (I) in such a way that no different ingredients and / or active ingredients are perceptible to the naked eye.
- the grain structure of the solids used can of course still be recognized.
- Heterogeneous shaped bodies are accordingly understood to mean those which do not have a homogeneous distribution of the ingredients present in addition to the ingredient (I).
- heterogeneous shaped bodies can be produced, for example, by the different ingredients having different colors and / or carrying a different fragrance component.
- Another case, which according to the invention is to be counted as the non-uniform (heterogeneous) molded bodies comprises an embodiment in which a molded body is pressed which, in addition to the area with the ingredient (I), has several layers (phases), that is to say at least two layers having. It is e.g. B. possible that these different layers have different disintegration and dissolution rates and / or carry different ingredients. This can result in advantageous application properties of the molded body. If, for example, ingredients are contained in the moldings that mutually influence each other, it is possible to separate them.
- a defined sequence of cleaning conditions is to be created in a machine, it is possible to integrate one (or more) component (s) in a (or) the more rapidly disintegrating and / or faster dissolving layer and the other (n) component Incorporate into one or more slowly disintegrating layers so that one component can act with a lead time or has already reacted when another goes into solution.
- a preferred embodiment of the invention consists in that in addition to the area with the ingredient (I) there are two further phases. It is particularly advantageous if the volume ratios of the two further phases are between 10: 1 and 1:10, preferably between 5: 1 and 1: 5, particularly preferably between 2: 1 and 1: 2. Another particularly preferred embodiment is characterized in that three or more further phases are present.
- the layer structure of the molded body can take place in a stack-like manner, with the inner layer (s) already loosening at the edges of the molded body when the outer layers have not yet been completely detached or disintegrated; however, a complete and / or partial covering of the inner layer (s) can also be achieved by the layers lying further outwards, which leads to a prevention and / or delay in the early dissolution of components of the inner layer (s).
- a tablet consists of at least three layers, that is to say two outer and at least one inner layer, at least one of the inner layers containing a peroxy bleach, while in the case of the tablet in the form of a tablet, the two outer layers and in the case of the shell-like one
- the outermost layers of the tablet are free of peroxy bleach. It is also possible to spatially separate peroxy bleaching agents and any bleach activators or bleach catalysts and / or enzymes present in a tablet / molded article. Such configurations have the advantage that there would be no fear of undesired interactions in the inventive moldings.
- Another cheap and preferred embodiment of the invention is that one of the bleaching component or components, especially the chlorine component, is not assembled together with the perfume component in one phase.
- Another cheap and preferred embodiment of the invention is that the silver protection component is not made up with one or more of the bleaching components.
- Another cheap and preferred embodiment of the invention is that one of the component or components for solubility control is packaged together with the bleach activator.
- Another cheap and preferred embodiment of the invention is that one of the component or components for solubility control is packaged together with the enzymes.
- Another cheap and preferred embodiment of the invention is that one of the component or components for solubility control is packaged together with the bleach.
- Another cheap and preferred embodiment of the invention is that one of the component or components for solubility trolleys is assembled together with the silver protection component.
- Another cheap and preferred embodiment of the invention is that one of the component or components for solubility control together with at least 50 wt .-%, preferably more than 70 wt .-%, particularly more than 90 wt .-% of a surfactant or all of them - is mixed.
- the agents according to the invention are produced by the customary methods of molding production.
- the ingredient (s) (I) in the form of a liquid generally through solution and / or melt
- a viscosity of more than 1500 mPas preferably more than 2000 mPas, particularly preferably between 2000 and 15000 mPas, very particularly preferably between 2500 and 7000 mPas and extremely preferably between 3000 and 4000 mPas has proven particularly useful.
- meltable carrier substances have proven particularly effective. In principle, this includes all substances with a solidification point at or especially above room temperature.
- Non-ionic surfactants (Dehypon® LT 104, Dehypon® LS 54, Dehydol® LS 30, Lutensol® AT 80), polyethylene glycols with different molecular weights (PEG 400, 12000), soaps (Lorol® C 16 ), Stearates (Cutina® GMS), but also thickened sodium hydroxide solution and meltable salts, such as sodium carbonate - decahydrate.
- Waxes are particularly preferred as meltable components in the context of the present invention. "Waxing” is understood to mean a number of natural or artificially obtained substances which generally melt above 40 ° C.
- waxes without decomposition and which are relatively low-viscosity and not stringy even a little above the melting point. They have a strongly temperature-dependent consistency and solubility.
- the waxes are divided into three groups according to their origin, natural waxes, chemically modified waxes and synthetic waxes.
- Natural waxes include, for example, vegetable waxes such as candeliu wax, carnauba wax, japan wax, esparto grass wax, korl wax, guaruma wax, rice germ oil wax, sugar toluene wax, ouricury wax, or montan wax, animal waxes such as beeswax, shellac wax, walnut, lanolin (wool wax), mineral wax, or shearling fat Ceresin or ozokerite (earth wax), or petrochemical waxes such as petrolatum, paraffin waxes or micro waxes.
- vegetable waxes such as candeliu wax, carnauba wax, japan wax, esparto grass wax, korl wax, guaruma wax, rice germ oil wax, sugar toluene wax, ouricury wax, or montan wax
- animal waxes such as beeswax, shellac wax, walnut, lanolin (wool wax), mineral wax, or shearling fat Cer
- the chemically modified waxes include hard waxes such as montan ester waxes, Sassol waxes or hydrogenated jojoba waxes.
- Synthetic waxes are generally understood to mean polyalkylene waxes or polyalkylene glycol waxes.
- Wax alcohols are high molecular weight, water-insoluble fatty alcohols with more than 28 to 40 carbon atoms.
- the wax alcohols occur, for example, in the form of wax esters of higher molecular fatty acids (wax acids) as the main component of many natural waxes.
- wax alcohols are lignoceryl alcohol (1-tetracosanol) or melissyl alcohol.
- the fusible component can optionally also contain wool wax alcohols, which means trite phene and steroid alcohols, for example lanolin.
- fatty acid glycerol esters or fatty acid alkanolamides but also, if appropriate, water-insoluble or only slightly water-soluble polyalkylene glycol compounds can likewise be used at least in part as part of the meltable component.
- the fusible component preferably contains paraffin wax. That is, at least 50% by weight of the fusible component, preferably more Paraffin wax exist. Paraffin wax contents in the coating of approximately 60% by weight, approximately 70% by weight or approximately 80% by weight are particularly suitable, with even higher proportions of, for example, more than 90% by weight being particularly preferred. In a special embodiment of the invention, the fusible component consists exclusively of paraffin wax.
- Paraffin waxes have the advantage over the other natural waxes mentioned in the context of the present invention that there is no hydrolysis of the waxes in an alkaline detergent environment (as is to be expected, for example, from the wax esters), since paraffin wax contains no hydrolyzable groups.
- Paraffin waxes consist mainly of alkanes, as well as low proportions of iso- and cycloalkanes.
- the paraffin to be used according to the invention preferably has essentially no constituents with a melting point of more than 70 ° C., particularly preferably of more than 60 ° C. Portions of high-melting alkanes in the paraffin can leave undesired wax residues on the surfaces to be cleaned or the goods to be cleaned if the melting temperature in the detergent solution drops below this. Such wax racks usually lead to an unsightly appearance of the cleaned surface and should therefore be avoided.
- the coating according to the invention preferably contains at least one paraffin wax with a melting point of about 57 ° C. to about 60 ° C.
- paraffin wax content of alkanes, isoalkanes and cycloalkanes which are solid at ambient temperature is preferably as high as possible.
- the more solid wax components present in a wax at room temperature the more useful it is within the scope of the present invention.
- With increasing proportion of solid wax components the resilience of the coating to impacts or friction on other surfaces increases, which leads to a longer-lasting protection of the coated particles.
- High .Share of oils or liquid wax components can weaken the coating, which opens pores and the with the Meltable component assembled particles are exposed to the environmental influences mentioned above.
- the solidified, meltable component can break under impact or friction.
- additives can optionally be added to the fusible component. Suitable additives must be able to be mixed completely with the molten wax, must not significantly change the melting range of the coating, must improve the elasticity of the solidified fusible component at low temperatures, must not and must not generally increase the permeability of the solidified fusible component to water or moisture do not increase the viscosity of the melt of the coating material to such an extent that processing becomes difficult or even impossible.
- Suitable additives which reduce the brittleness of a sheath consisting essentially of paraffin at low temperatures are, for example, EVA copolymers, hydrogenated resin acid methyl ester, polyethylene or copolymers of ethyl acrylate and 2-ethylhexyl acrylate.
- the fusible component can also contain one or more of the above-mentioned waxes or wax-like substances as the main constituent.
- the mixture forming the cover should be such that the cover is at least largely water-insoluble.
- the solubility in water should not exceed about 10 mg 1 at a temperature of about 30 ° C. and should preferably be below 5 mg / 1.
- parts of the molded body and / or components of the molded body are treated by irradiation with microwaves in order to positively influence strength, moisture content and solubility. But a simple pressing of the components is also possible.
- microtabs and molded articles of smaller dimensions than the final molded article can also be used.
- Special ingredients (I) which are used in the context of the invention are the surfactants.
- all surfactants can be used as surfactants.
- the alkoxylated alcohols, particularly the ethoxylated and / or propoxylated ones, the alkyl polyglycosides and the alkyl polyglucamides are particularly preferred.
- alkoxylated alcohols to mean the reaction products of alkylene oxide, preferably ethylene oxide, with alcohols, preferably in the sense of the present invention the longer-chain alcohols (C 1 -C 1, preferably between C 12 and C 16 , such as Cn-, C ⁇ 2 -, C ⁇ -, C ⁇ 4 -, C ⁇ 5 -, C ⁇ 6 -, C ⁇ 7 - and C ⁇ 8 alcohols).
- C 1 -C 1 preferably between C 12 and C 16 , such as Cn-, C ⁇ 2 -, C ⁇ -, C ⁇ 4 -, C ⁇ 5 -, C ⁇ 6 -, C ⁇ 7 - and C ⁇ 8 alcohols.
- n moles of ethylene oxide and one mole of alcohol form a complex mixture of addition products of different degrees of ethoxylation, depending on the reaction conditions.
- Another embodiment is the use of mixtures of the alkylene oxides, preferably the mixture of ethylene oxide and propylene oxide.
- a final etherification with short-chain alkyl groups can also lead to the "closed" alcohol ethoxylate class, which can also be used in the context of the invention.
- Highly preferred for the purposes of the present invention are highly ethoxylated fatty alcohols or their mixtures with end-capped fatty alcohol ethoxylates.
- the alkoxylated alcohols containing hydroxyl groups are particularly preferred, as described in EP 300 305, the disclosure of which is expressly incorporated here.
- these hydroxy mixed ethers have an excellent rinse aid effect. This applies particularly preferably in mixtures with other nonionic surfactants, such as Dehypon LS 54, and also in mixtures with Dehydol LS 4, but also in mixtures with hydroxy mixed ether and .APG.
- these surfactant mixtures even in a homogeneous mixture, decisively reduced the stress corrosion crack on plastic.
- Alkyl polyglycosides are surfactants which can be obtained by the reaction of sugars and alcohols according to the relevant procedures in preparative organic chemistry, with a mixture of monoalkylated, oligomeric or polymeric sugars depending on the type of preparation.
- Preferred alkyl polyglycosides can be alkyl polyglucosides, the alcohol being particularly preferably a long-chain fatty alcohol or a mixture of long-chain fatty alcohols and the degree of oligomerization of the sugars being between 1 and 10.
- Fatty acid polyhydroxylamides are acylated reaction products of the reductive amination rank of a sugar (glucose) with ammonia, whereby long-chain fatty acids, long-chain fatty acid esters or long-chain fatty acid chlorides are generally used as acylating agents.
- Secondary amides are formed when reducing with methylamine or ethylamine instead of with ammonia, such as. B. in S ⁇ FW-Journal, 119, (1993), 794-808.
- Carbon chain lengths of C 6 to C 12 in the fatty acid residue are preferably used.
- Special ingredients (I) which are used in the context of the invention are oxygen bleaching agents, preferably the alkali metal perborates and their hydrates and the alkali metal percarbonates, sodium perborate, as mono- or tetrahydrate, or sodium percarbonate and their hydrates preferably being used in the context of the invention.
- the persulphates can also be used.
- Typical oxygen bleaches are also organic peracids.
- the organic peracids used with preference include above all the excellently active phthalimidoperoxycaproic acid, but in principle all other known peracids can also be used.
- bleach activators are compounds which contain one or more N- or O-acyl groups, such as substances from the class of anhydrides, esters, imides and acylated imidazoles or oximes. Examples are tetraacetylethylenediamine TAED, tetraacetylmethylenediamine TAMD and tetraacetylhexylenediamine T.AHD, but also pen- taacetylglucose PAG, l, 5-diacetyl-2,2-dioxo-hexahydro-l, 3,5-triazine DADHT and isatoic anhydride ISA.
- N- or O-acyl groups such as substances from the class of anhydrides, esters, imides and acylated imidazoles or oximes. Examples are tetraacetylethylenediamine TAED, tetraacetylmethylenediamine TAMD and tetraacetylhexyl
- aliphatic peroxocarboxylic acids with preferably 1 to 10 C atoms, in particular 2 to 4 C atoms, and / or optionally substituted perbenzoic acid can be used as bleach activators.
- Suitable are substances which carry O- and / or N-acyl groups of the stated number of carbon atoms and / or optionally substituted benzoyl groups.
- Multi-acylated alkylenediamines in particular tetraacetylethylenediamine (T.AED), acylated triazine derivatives, in particular l, 5-diacetyl-2,4-dioxohexahydro-l, 3,5-triazine (D.ADHT), acylated glycolurils, in particular tetraacetylglycoluril, are preferred (TAGU), N-acylimides, especially N-nonanoylsuccinimide (NOSI), acylated phenol sulfonates, especially n-nonanoyl- or isononanoyloxybenzenesulfonate (n- or iso-NOBS), carboxylic acid anhydrides, especially phthalic anhydride, especially acylated trihydric alcohols, acylated polyhydric alcohols, koldiacetate, 2,5-diacetoxy-2,5-dihydrofuran,
- hydrophilically substituted acylacetals known from German patent application DE 196 16 769 and the acyl lactams described in German patent application DE 196 16 770 and international patent application WO 95/14075 are also preferably used.
- the combinations of conventional bleach activators known from German patent application DE 44 43 177 can also be used. Bleach activators of this type are present in the customary quantitative range, preferably in amounts of 1% by weight to 10% by weight, in particular 2% by weight to 8% by weight, based on the total agent.
- bleaching catalysts In addition to the conventional bleach activators listed above or in their place, those from European patent specifications EP 0 446 982 and Known EP 0 453 003 sulfonimines and / or bleach-enhancing transition metal salts or transition metal complexes may be included as so-called bleaching catalysts.
- the transition metal compounds in question include in particular the manganese, iron, cobalt, ruthenium or molybdenum salen complexes known from German patent application DE 195 29 905 and their N-analogue compounds known from German patent application DE 196 20 267 Manganese, iron, cobalt, ruthenium or molybdenum carbonyl complexes known from German patent application DE 195 36 082, the manganese, iron, cobalt, ruthenium, molybdenum, Titanium, vanadium and copper complexes with nitrogen-containing tripod ligands, the cobalt, iron, copper and ruthenium amine complexes known from German patent application DE 196 20 411, the M.
- German patent application DE 44 16 438 angan copper and cobalt complexes, the cobalt complexes described in European patent application EP 0 272 030, the manganese com. known from European patent application EP 0 693 550 plexes, the manganese, iron, cobalt and copper complexes known from European patent EP 0 392 592 and / or those described in European patent EP 0443 651 or European patent applications EP 0 458 397, EP 0 458 398, EP 0 549 271, EP 0 549 272, EP 0 544 490 and EP 0 544 519 described manganese complexes.
- bleach activators and transition metal bleach catalysts are known, for example, from German patent application DE 196 13 103 and international patent application WO 95/27775.
- Bleach activators from the group of multi-acylated alkylenediamines in particular tetraacetylethylene diamine (TAED), N-acylimides, in particular N-nonanoylsuccinimide (NOSI), acylated phenolsulfonates, in particular n-nonanoyl- or isononanoyloxybenzenesulfonate (NOBS) or isobenzene sulfonate (N-) iso MMA, preferably in amounts of up to 10% by weight, in particular 0J% by weight to 8% by weight, particularly 2 to 8% by weight and particularly preferably 2 to 6% by weight, based on the total composition, used.
- TAED tetraacetylethylene diamine
- NOSI N-nonanoylsuccinimide
- Bleach-boosting transition metal complexes in particular with the central atoms Mn, Fe, Co, Cu, Mo, V, Ti and / or Ru, preferably selected from the group consisting of manganese and / or cobalt salts and / or complexes, particularly preferably cobalt (ammin) - Complexes, the cobalt (acetate) complexes, the cobalt (carbonyl) complexes, the chlorides of cobalt or manganese, of manganese sulfate are used in conventional amounts, preferably in an amount up to 5% by weight, in particular from 0.0025% by weight to 1% by weight and particularly preferably from 0.01% by weight to 0.25% by weight, in each case based on the entire funds. But in special cases, more bleach activator can be used.
- Dishwashing detergents according to the invention can contain corrosion inhibitors as ingredient (I) to protect the items to be washed or the machine, silver protection agents in particular being particularly important in the field of automatic dishwashing.
- corrosion inhibitors as ingredient (I) to protect the items to be washed or the machine
- silver protection agents in particular being particularly important in the field of automatic dishwashing.
- the known subsets of the prior art such as. B. described in DE 43 25 922, DE 41 28 672 or DE 43 38 724.
- silver protection agents selected from the group consisting of the triazoles, the benzotriazoles, the bisbenzotriazoles, the aminotriazoles, the alkylaminotriazoles and the transition metal salts or complexes can be used.
- Benzotriazole and / or alkylaminotriazole are particularly preferably to be used.
- Agents containing active chlorine which can significantly reduce the corroding of the silver surface, are also frequently found in Remiger formulation oranges.
- chlorine-free cleaners especially oxygen and nitrogen-containing organic redox-active compounds, such as di- and trihydric phenols, e.g. B. hydroquinone, pyrocatechol, hydroxyhydroquinone, gallic acid, phloroglucin, pyrogallol or derivatives of these classes of compounds.
- Salt-like and complex-like inorganic compounds such as salts of the metals Mn, Ti, Zr, Hf, V, Co and Ce, are also frequently used.
- transition metal salts which are selected from the group consisting of manganese and / or cobalt salts and / or complexes, particularly preferably the cobalt (amine) complexes, the cobalt (acetate) complexes, the cobalt (carbonyl) complexes , the chlorides of cobalt or manganese and manganese sulfate.
- Zinc compounds can also be used to prevent corrosion on the wash ware.
- Special ingredients (I) which are used in the context of the invention are substances which prevent the re-soiling of surfaces and / or facilitate the detachment of dirt after a single application (so-called “soil release compounds”).
- the soil release compounds used according to the invention include all compounds known in the prior art.
- Cationic polymers such as those used for. B. are known from the following publications: In EP-A-0 167 382, EP-A-0 342 997 and DE-OS-26 16 404 cleaning agents are added cationic polymers in order to achieve a streak-free cleaning of the surfaces.
- EP-A-0 167 382 describes liquid detergent compositions which can contain cationic polymers as thickeners. Hydroxypropyltrimethylammonium guar; Copolymers of .Aminoethyl methacrylate and acrylamide and copolymers of dimethyldiallylammonium chloride and acrylamide are described.
- EP-A-0 342 997 describes all-purpose cleaners which can contain cationic polymers, in particular polymers with imino grapples being used.
- DE-OS-26 16 404 describes cleaning agents for glass which contain cationic cellulose derivatives.
- the addition of the cationic cellulose derivatives in the agents a better drainage of the water in order to obtain streak-free cleaned glass.
- EP-A-0 467 472 e.g. B. cleaning agents for hard surfaces which contain cationic homo- and / or copolymers as soil-release polymers. These polymers have quaternized ammonium alkyl methacrylate groups as monomer units. These connections are used to equip the surfaces in such a way that the soiling can be removed more easily during the next cleaning process.
- the cationic polymers are particularly preferably selected from cationic polymers of copolymers of monomers such as trialkylammonium alkyl (meth) acrylate or acrylamide; Dialkyldiallyldiammonium salts; polymer-analogous reaction products of ethers or esters of polysaccharides with ammonium side groups, in particular guar, cellulose and starch derivatives; Polyadducts of ethylene oxide with .ammonium grapples; quaternary ethylene imine polymers and polyesters and polyamides with quaternary side groups as soil release compounds.
- monomers such as trialkylammonium alkyl (meth) acrylate or acrylamide; Dialkyldiallyldiammonium salts; polymer-analogous reaction products of ethers or esters of polysaccharides with ammonium side groups, in particular guar, cellulose and starch derivatives; Polyadducts of ethylene oxide with .ammonium
- enzymes based on the entire preparation can be added to the cleaning agent in order to increase the performance of the cleaning agents or to guarantee the same quality of cleaning performance under milder conditions.
- the most commonly used enzymes include lipases, amylases, cellulases and proteases.
- Preferred proteases are e.g. B.
- BL.AP®140 from Biozym
- Optimase®-M-440 and Opticlean®-M-250 from Solvay Enzymes
- Maxacal®CX and Maxapem® or Esperase® from Gist Brocades or Savinase® from Novo.
- Particularly suitable cellulases and lipases are Celluzym® 0.7 T and Lipolase® 30 T from Novo Nordisk.
- Amylase-LT® from Solvay Enzymes or Maxamyl® P5000 from Gist Brocades find particular use as amylases.
- Other enzymes can also be used.
- all of the ingredients (I) described above can also take on the function of other ingredients if the condition of the inventive area is met by other ingredients.
- water-soluble and water-insoluble builders can be used especially for binding calcium and magnesium.
- Water-soluble builders are preferred because they generally have less tendency to form insoluble residues on dishes and hard surfaces.
- Customary builders which can be present in the scope of the invention between 10 and 90% by weight, based on the entire preparation, are the low molecular weight polycarboxylic acids and their salts, the homopolymeric and copolymeric polycarboxylic acids and their salts, the carbonates, phosphates and silicates .
- Water-insoluble builders include the zeolites, which can also be used, as well as mixtures of the abovementioned builder substances.
- Trisodium citrate and / or pentasodium tripolyphosphate and / or sodium carbonate and / or sodium bicarbonate and / or gluconates and / or silicate builders from the class of disilicate and / or metasilicate are preferably used.
- Alkali carriers can be present as further constituents.
- a builder system containing a mixture of tripolyphosphate and sodium carbonate is particularly preferred.
- a builder system containing a mixture of tripolyphosphate and sodium carbonate and sodium disilicate is also particularly preferred.
- the areas of the molded body can be colored. It is particularly preferred if one or more or all areas of the molded body are colored differently in the molded body. In one special embodiment of the molded body, the color is red. In another special embodiment of the molded body, the color is green. In another special embodiment of the molded body, the color is yellow. In another special embodiment of the molded body, the color is a mixture of different colors.
- the storage stability of the molded body is particularly important. It is particularly preferred according to the invention if the weight increase in the area of the ingredient (I) when stored under normal household conditions, ie. H. between 15 and 30 ° C. and between 5 and 55% atmospheric humidity, preferably 15 and 35% atmospheric humidity for a period of 30 days, preferably 60 days, particularly preferably 90 days, not more than 50% by weight, preferably not more than 40% %, very particularly preferably not more than 30% by weight, extremely preferably not more than 20% by weight and extremely preferably not more than 10% by weight, at best not more than 5% by weight.
- normal household conditions ie. H. between 15 and 30 ° C. and between 5 and 55% atmospheric humidity, preferably 15 and 35% atmospheric humidity for a period of 30 days, preferably 60 days, particularly preferably 90 days, not more than 50% by weight, preferably not more than 40% %, very particularly preferably not more than 30% by weight, extremely preferably not more than 20% by weight and extremely preferably not more than 10% by weight, at best not more
- the loss of active substance of the ingredient (I) when stored under normal household conditions ie between 15 and 30 ° C. and between 5 and 55% atmospheric humidity, preferably 15 and 35% atmospheric humidity for a period of 30 days , preferably 60 days, particularly preferably 90 days not more than 50% by weight, preferably not more than 40% by weight, very particularly preferably not more than 30% by weight, extremely preferably not more than 20% by weight and most preferably not more than 10% by weight, at best not more than 5% by weight.
- the absorption maximum of a 1% solution of a colored area or a colored component during storage under normal household conditions ie between 15 and 30 ° C.
- hydroxy mixed ethers in particular show outstanding rinse aid effects and reduce stress corrosion cracking on plastics. Furthermore, they have the advantageous property that their wetting behavior is constant over the entire usual temperature range.
- the use of the substances mentioned as a rinse aid component in automatic dishwashing detergents has hitherto not been described in the prior art. So far, only pure “cleaning agents” or pure “rinse aid” for automatic dishwashing have been disclosed.
- Another object of the present invention is therefore on the one hand the use of hydroxy mixed ethers and / or mixtures of hydroxy mixed ethers and nonionic surfactants as a rinse aid component in automatic dishwashing detergents and on the other hand the use of hydroxy mixed ethers and / or mixtures of hydroxy mixed ethers and nonionic surfactants as a component for preventing stress corrosion cracking in machine dishwashers Dishwashing detergents.
- hydroxy mixed ethers not alone, but in a mixture with other surfactants, preferably nonionic surfactants and in particular with nonionic surfactants from the group of ethoxylated fatty alcohols.
- Uses which are characterized in that the hydroxy mixed ethers in a mixture with fatty alcohols Thoxylates are therefore preferred.
- propoxylated or ethoxylated and propoxylated fatty alcohols can also be used in addition to the ethoxylated fatty alcohols.
- Such preferred uses are characterized in that the hydroxy mixed ethers are present in a mixture with fatty alcohol ethoxy propoxylates.
- the following recipes were mixed and pressed into shaped bodies.
- the ingredients in parentheses are examples of the substance class but can be replaced by other substances listed in the application.
- the frame formulations represent preferred areas of the invention.
- the builder system of the framework recipe above can also be composed as follows (all other ingredients are the same as in a).
- each formulation can also be the constituents of an individual phase, ie the proportions then do not relate to the overall formulation as usual, but to the composition of the individual phase.
- each of the recipes can also contain other ingredients commonly used in MGSM (e.g. fillers, preservatives, etc.) in extremely small quantities, with the other ingredients being proportionately varied accordingly.
- a preferred embodiment of the molded body of the first speech contains a depression in a tablet, this depression containing the ingredient (I).
- the production takes place in such a way that a depression is embossed into a molded body and this depression is filled.
- the embossing can be done on a Korsch rotary press.
- a tablet press from Fette was used.
- a round tablet shape (26 X 36 mm) was selected and embossed on one side with a stamp 5 mm deep, the base area being chosen such that a volume of 1 ml could be filled in and the tablet subsequently had a smooth surface.
- a liquid mixture of paraffin and an active ingredient (I) in the present case surfactant (Dehypon LS54, hydroxy mixed ether, mixtures of the two classes of substances) was then poured in and allowed to cool. This cooling can be supported by conventional apparatus methods.
- the ingredient (I) according to the invention was previously reduced in quantity in the corresponding recipe which surrounds the filled area and was omitted in the surrounding areas in the examples and investigations at hand.
- the special properties of the agents according to the invention were checked by technically untrained persons under practical conditions in comparison to homogeneous tablets. Apart from instructions for the dosage and general safety instructions, no influence was taken on the handling of the agents by the group of people in standard dishwashers. This comparison test turned out to be particularly good. The cleaning results were rated as particularly favorable here. In an experiment, samples analogous to Ra or Val were used which contained surfactants as active ingredient (I) once in a homogeneous distribution in the tablet and once according to approach 1, so that the surfactant component was largely separated from other components. The cleaning results were very good.
- the rinse aid results were also checked. With the effect of using a mixture of surfactant (hydroxy mixed ether) and paraffin in a standard program at 55 ° C, the results were better than with molded articles without area (I), homogeneously distributed component (I) and commercially available cleaners. The results show a positive influence of the paraffin. Changing the melting range of the paraffin also has an effect on the washing result.
- melt emulsions of different surfactants were produced in coating substances, which prove the positive effects.
- trough-shaped bodies weight: 24 g
- Table 1 shows the composition (in% by weight, based on the premix) and thus the mold body:
- melt dispersions SDE 1 to 5 were produced, the composition (% by weight, based on the melt) of which is given in the table below:
- the melt emulsions were poured into the moldings in the manner mentioned above and allowed to cool.
- the moldings had a weight of 24 g before being infested and were each filled with 1.3 g of the melt emulsion.
- the cleaning performance (rinsing effect) of the molded bodies El to E5 filled with the melt emulsions SDE 1 to SDE 5 was tested on different substrates (plates, glasses, knives, plastic plates). For this purpose, the soiled objects were cleaned in a normal household dishwasher, whose rinse aid tank was empty:
- the rinse aid effect of the detergents was carried out visually by experts and was graded, the score "0" meaning water stains and no difference to rinsing without rinse aid on a scale of 0-8 and "8" meaning absolutely clean.
- the rinse aid effects were measured for washing conditions 55 ° C / 16 ° d water hardness in the main rinse cycle (ie "hard conditions").
- a Miele G 590 with a universal program was used as the dishwasher.
- the table below shows the rinse aid results achieved with agents El to E5 compared to an unfilled molded article V
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Abstract
The present invention relates to moulded bodies containing builder substances, alkali carriers, bleaching agents, enzymes and surfactants. Particularly powerful moulded bodies with a high degree of storage stability, a good scent profile and a defined solubility profile are obtained when an area corresponding to no more than 40 vol. % of the moulded body contains more than 80 wt. % of the total amount of an active substance (I) contained in the moulded body with an ingredient from the group of surfactants.
Description
Geschirrspülmittelfoimkörper mit Tensiden Dishwashing detergent film body with tensides
Die Erfindung betrifft wasch- oder reinigungsaktive Formkörper, in erster Linie Tabletten wie Geschirrspülmitteltabletten, Waschmitteltabletten, Bleichmitteltabletten, Fleckensalztabletten oder Wasserenthärtungstabletten für den Gebrauch im Haushalt, insbesondere für den maschinellen Gebrauch, sowie ein Verfahren zur Herstellung dieser Formköφer und ihrer Verwendung.The invention relates to washing or cleaning active moldings, primarily tablets such as dishwasher tablets, detergent tablets, bleach tablets, stain remover tablets or water softening tablets for use in the home, in particular for mechanical use, and a process for producing these moldings and their use.
Wasch- oder reinigungsaktive Formkörper, insbesondere Tabletten, besitzen gegenüber pulverföimigen Mitteln eine Reihe von Vorteilen, wie eine vorteilhafte Handhabung, eine einfache Dosierung, sowie geringer Bedarf an Verpackungsvolumina.Shaped or active cleaning moldings, in particular tablets, have a number of advantages over powder-form agents, such as advantageous handling, simple dosing and low packaging volume requirements.
Probleme ergeben sich jedoch dadurch, daß zur Erreichung einer hinreichenden Form- und Bruchbeständigkeit beim Verpressen der pulverföimigen Bestandteile verhältnismäßig hohe Preßdrucke angewendet werden müssen. Aufgrund der starken Verdichtung weisen derartige Tabletten vielfach eine unzureichende Lagerstabilität bezüglich empfindlicher Inhaltsstoffe (Bleiche, Parfüm, Enzyme, Silberschutzmittel, Farbstoffe, Tenside), eine verringerte Leistung (besonders bei .Ansc.hmutzungen wie Tee, Milch, Stärke) im Vergleich zu vergleichbaren Mengen .Aktivsubstanz in anderer Darbietungsform, in manchen Fällen verbesserungsfähige Schutz empfindlicher zu reinigender Materialien und verschlechterte Zerfalls- und Löseeigenschaften bei ihrer Anwendung auf.Problems arise, however, in that relatively high compression pressures have to be used to achieve adequate dimensional stability and fracture resistance when pressing the powdery components. Due to the high degree of compaction, such tablets often have inadequate storage stability with regard to sensitive ingredients (bleach, perfume, enzymes, silver preservatives, dyes, surfactants), a reduced performance (especially in the case of soiling such as tea, milk, starch) in comparison to comparable amounts .Active substance in a different form of presentation, in some cases there is room for improvement in the protection of sensitive materials to be cleaned and deteriorated disintegration and dissolving properties when used.
Bei einigen Patentschriften des Standes der Technik sollen einige dieser Probleme ver- meidlich gelöst sein.Some of the prior art patents are said to avoid some of these problems.
Oft kann aber der Verbraucher diese dort beschriebenen Leistungsvorteile nicht nachvollziehen. Daher besteht ein wichtiges Problem für .Anbieter von wasch- oder reinigungsaktiven Formkörpern darin Verbraucher zufriedenzustellen.However, the consumer is often unable to understand the performance advantages described there. There is therefore an important problem for providers of shaped washing or cleaning bodies in satisfying consumers.
Aufgabe der vorliegenden Erfindung war es also leistungsstarke, leicht handhabbare wasch- oder reinigungsaktive Formkörper, vor allem Geschirrspülmitteltabletten, Waschmitteltabletten, Fleckensalztabletten oder Wasserenthärtungstabletten für den Gebrauch im
Haushalt, insbesondere für den maschinellen Gebrauch mit hoher Lagerstabilität, geringem Verpackungsaufwand, gutem Duftprofil und definiertem Löslichkeitsprofil bereitzustellen, welche vor allem eine hohe Kundenzufriedenheit bewirken.It was therefore an object of the present invention to provide high-performance, easy-to-handle washing or cleaning-active moldings, especially dishwasher tablets, detergent tablets, stain remover tablets or water softening tablets for use in To provide household, especially for machine use with high storage stability, low packaging costs, good fragrance profile and defined solubility profile, which above all result in high customer satisfaction.
Dies wurde überraschend durch einen Formköper gelöst, bei dem ein Inhaltsstoff (I) überwiegend in einem definierten Bereich bereitgestellt wurde, wobei dieser Bereich nicht mehr als 40 Vol-% des Formköipers darstellt.This was surprisingly solved by a molded article in which an ingredient (I) was predominantly provided in a defined area, this area not representing more than 40% by volume of the molded article.
Gegenstand der Anmeldung ist daher ein Formkörper enthaltend Builderstoffe, Alkaliträger, Bleichmittel und Enzyme, dadurch gekennzeichnet, daß in einem Bereich nicht größer als 40 Vol.-%, mehr als 80 Gew.-%, einer Aktivsubstanz (I) mit einem Bestandteil aus der Gruppe der Tenside enthalten ist.The application therefore relates to a molded article containing builder substances, alkali carriers, bleaches and enzymes, characterized in that in an area not greater than 40% by volume, more than 80% by weight, of an active substance (I) with a constituent from the Group of surfactants is included.
Der Inhaltsstoff (I) kann dabei neben dem Tensid auch noch mindestens ein Bleichmittel aus der Gruppe der Chlor und/oder Sauerstoffbleicbmittel, ein Bleichaktivator, ein Silberschutzmittel und/oder eine Soil-Release- Verbindung, ein Enzym oder eine Komponente oder ein Compound zur Löslichkeitskontrolle enthalten. Der Inhaltsstoff (I) kann aber auch ein Gemisch mehrerer dieser Bestandteile sein.In addition to the surfactant, the ingredient (I) can also contain at least one bleach from the group of chlorine and / or oxygen lead agents, a bleach activator, a silver protection agent and / or a soil release compound, an enzyme or a component or a compound for solubility control contain. The ingredient (I) can also be a mixture of several of these ingredients.
Besonders bevorzugt ist es, wenn der Inhaltsstoff (I) ein Gemisch aus einer Komponente, bzw. einem Compound zur Löslichkeitskontrolle einem Tensid und mindestens einem weiteren Inhaltsstoff aus der Gruppe bestehend aus Bleichmittel und/oder Bleichaktivator und/oder Silberschutzmittel und/oder Soil-Release- Verbindung und/oder Enzym und/oder ein Tensid ist.It is particularly preferred if the ingredient (I) is a mixture of a component or a compound for solubility control, a surfactant and at least one other ingredient from the group consisting of bleaching agent and / or bleach activator and / or silver protective agent and / or soil release - Compound and / or enzyme and / or a surfactant.
Entscheidenden Einfluß auf die Eigenschaften der Tablette können auch die Löslichkeit des Bereiches mit dem Inhaltsstoff (I), die Oberfläche und die Art der Verpressung und die Lagerstabilität haben.The solubility of the area with the ingredient (I), the surface and the type of compression and the storage stability can also have a decisive influence on the properties of the tablet.
Günstig ist es im Sinne der vorliegenden Erfindung wenn der Bereich mit mehr als 80 Gew.-%, bevorzugt mehr als 90 Gew.-%, besonders bevorzugt mehr als 95 Gew.-%, ganz besonders bevorzugt der Gesamtmenge eines vorhandenen Inhaltsstoffes (I) in genau drei Raumrichtungen von anderen Inhaltsstoffen des Formkörpers umgeben ist.For the purposes of the present invention, it is favorable if the range contains more than 80% by weight, preferably more than 90% by weight, particularly preferably more than 95% by weight, very particularly preferably the total amount of an ingredient (I) present in exactly three spatial directions is surrounded by other ingredients of the molded body.
Bevorzugt im Rahemn der vorliegenden Erfindung ist ebenfalls, wenn mindestens ein Bereich mit mehr als 80 Gew.-%, bevorzugt mehr als 90 Gew.-%, besonders bevorzugt mehr als 95 Gew.-%, ganz besonders bevorzugt der Gesamtmenge eines vorhandenen Inhalts-
stoffes (I) vorliegt, der sich um mehr als 5 %, bevorzugt mehr als 10 %, ganz besonders bevorzugt mehr als 25 %, ganz besonders bevorzugt mehr als 50 % und äußerst bevorzugt mehr als 100 % schneller löst als der und oder die restlichen Bereiche des Formkörpers.It is also preferred in the context of the present invention if at least one region with more than 80% by weight, preferably more than 90% by weight, particularly preferably more than 95% by weight, very particularly preferably the total amount of content present Substance (I) is present, which dissolves more than 5%, preferably more than 10%, very particularly preferably more than 25%, very particularly preferably more than 50% and most preferably more than 100% faster than the one or more Areas of the molded body.
Positiv ist ebenfalls wenn in einem Bereich mit nicht mehr als 40 % der Oberfläche, bevorzugt zwischen 5 und 30 %, besonders bevorzugt zwischen 10 und 25 %, ganz besonders bevorzugt zwischen 15 und 20 Vol.-% des Foimköipers me.hr als 80 Gew.-%, bevorzugt mehr als 90 Gew.-%, besonders bevorzugt mehr als 95 Gew.-%, ganz besonders bevorzugt die Gesamtmenge eines vorhandenen Inhaltsstoffes (I) enthalten ist.It is also positive if in an area with no more than 40% of the surface, preferably between 5 and 30%, particularly preferably between 10 and 25%, very particularly preferably between 15 and 20% by volume of the foam body, more than 80% by weight %, preferably more than 90% by weight, particularly preferably more than 95% by weight, very particularly preferably the total amount of an ingredient (I) present.
Einen wünschenswerten Einfluß auf das Gesamtergebnis kann man auch erzielen, wenn die Gewichtszunahme des Bereichs enthaltend mehr als 80 Gew.-% des Inhaltsstcffes (I) bei Lagerung unter normalen Haushaltsbedingungen, d. h. zwischen 15 und 30 °C und zwischen 5 und 55 % Luftfeuchtigkeit, bevorzugt 15 und 35 % Luftfeuchtigkeit für die Dauer von 30 Tagen, bevorzugt 60 Tagen, besonders bevorzugt 90 tagen nicht mehr als 50 Gew.- %, bevorzugt nicht mehr als 40 Gew.-%, ganz besonders bevorzugt nicht mehr als 30 Gew.-%, außerordentlich bevorzugt nicht mehr als 20 Gew.-% und äußerst bevorzugt nicht mehr als 10 Gew.-% günstigstenfalls nicht mehr als 5 Gew.-% beträgt.A desirable influence on the overall result can also be achieved if the weight increase of the area containing more than 80% by weight of the content (I) when stored under normal household conditions, i. H. between 15 and 30 ° C and between 5 and 55% atmospheric humidity, preferably 15 and 35% atmospheric humidity for a period of 30 days, preferably 60 days, particularly preferably 90 days, not more than 50% by weight, preferably not more than 40% %, very particularly preferably not more than 30% by weight, extremely preferably not more than 20% by weight and extremely preferably not more than 10% by weight, at best not more than 5% by weight.
Einen wünschenswerten Einfluß auf das Gesamtergebnis kann man auch erzielen, wenn der Verlust an .Aktivsubstanz (I) des Bereichs enthaltend mehr als 80 Gew.-% eines Inhaltsstoffes bei Lagerang unter normalen Haushaltsbedingungen, d. h. zwischen 15 und 30 °C und zwischen 5 und 55 % Luftfeuchtigkeit, bevorzugt 15 und 35 % Luftfeuchtigkeit für die Dauer von 30 Tagen, bevorzugt 60 Tagen, besonders bevorzugt 90 tagen nicht mehr als 50 Gew.-%, bevorzugt nicht mehr als 40 Gew.-%, ganz besonders bevorzugt nicht mehr als 30 Gew.-%, außerordentlich bevorzugt nicht mehr als 20 Gew.-% und äußerst bevorzugt nicht mehr als 10 Gew.-% günstigstenfalls nicht mehr als 5 Gew.-% beträgt.A desirable influence on the overall result can also be achieved if the loss of .active substance (I) in the region containing more than 80% by weight of an ingredient when stored under normal household conditions, i. H. between 15 and 30 ° C. and between 5 and 55% atmospheric humidity, preferably 15 and 35% atmospheric humidity for a period of 30 days, preferably 60 days, particularly preferably 90 days, not more than 50% by weight, preferably not more than 40% %, very particularly preferably not more than 30% by weight, extremely preferably not more than 20% by weight and extremely preferably not more than 10% by weight, at best not more than 5% by weight.
Einen wünschenswerten Einfluß auf das Gesamtergebnis kann man auch erzielen, wenn das Absoφtionsmaximum einer 1% igen Lösung eines gefärbten Bereichs oder einer gefärbten Komponente bei Lagerung unter normalen Haushaltsbedingungen, d. h. zwischen 15 und 30 °C und zwischen 5 und 55 % Luftfeuchtigkeit, bevorzugt 15 und 35 % Luftfeuchtigkeit für die Dauer von 30 Tagen, bevorzugt 60 Tagen, besonders bevorzugt 90 tagen nicht mehr als 100 Wellenzahlen, bevorzugt nicht mehr als 50 Wellenzahlen, ganz besonders bevorzugt nicht mehr als 30 Wellenzahlen, außerordentlich bevorzugt nicht
melir als 20 Wellenzahlen und äußerst bevorzugt nicht mehr als 10 Wellenzahlen günstigstenfalls nicht mehr als 5 Wellenzahlen beträgt.A desirable influence on the overall result can also be achieved if the absorption maximum of a 1% solution of a colored area or a colored component when stored under normal household conditions, ie between 15 and 30 ° C. and between 5 and 55% atmospheric humidity, preferably 15 and 35% humidity for a period of 30 days, preferably 60 days, particularly preferably 90 days, not more than 100 wave numbers, preferably not more than 50 wave numbers, very particularly preferably not more than 30 wave numbers, extremely preferably not melir than 20 wavenumbers and most preferably not more than 10 wavenumbers, at best not more than 5 wavenumbers.
Gleichfalls positiv wirkt sich auf den erfindungsgemäßen Formköφer aus, wenn der Bereich mit mehr als 80 Gew.-%, bevorzugt mehr als 90 Gew.-%, besonders bevorzugt mehr als 95 Gew.-%, ganz besonders bevorzugt der Gesamtmenge eines vorhandenen Inhaltsstoffes (I) in genau drei Raumrichtungen von anderen Inhaltsstoffen des Formköφers umgeben ist.The molded body according to the invention also has a positive effect if the region with more than 80% by weight, preferably more than 90% by weight, particularly preferably more than 95% by weight, very particularly preferably the total amount of an ingredient present ( I) is surrounded by other ingredients of the molded body in exactly three spatial directions.
Löslichkeit:Solubility:
Die Löslichkeit kann dabei durch Komponenten und/oder Compounds zur Löslichkeitsbe- schleunigung (Sprengmittel) oder zur Löslichkeitsverzögerung beeinflußt werden.The solubility can be influenced by components and / or compounds to accelerate solubility (disintegrant) or to delay solubility.
Als Sprengmittel können alle im Stand der Technik bekannten Sprengmittel Verwendung finden. Besonders verwiesen wird auf Lehrbücher Römpp (9. Auflage, Bd. 6, S. 4440) und Voigt „Lehrbuch der pharmazeutischen Technologie" (6. Auflage, 1987). Besonders geeignet sind Substanzen wie Stärke, Cellulose und Cellulose-Derivate, Alginate, Dextrane, querveraetzte Polyvinylpyrrolidone und andere; Systeme aus schwachen Säuren und car- bonathaltigen Mitteln, insbesondere Citronensäure und Weinsäure in Kombination mit Hydrogencarbonat oder Carbonat sowie Polyethylenglykolsorbitanfettsäureester.All disintegrants known in the prior art can be used as disintegrants. Particular reference is made to the textbooks Rompp (9th edition, vol. 6, p. 4440) and Voigt "Textbook of pharmaceutical technology" (6th edition, 1987). Substances such as starch, cellulose and cellulose derivatives, alginates, Dextrans, cross-linked polyvinylpyrrolidones and others; systems of weak acids and carbonate-containing agents, in particular citric acid and tartaric acid in combination with bicarbonate or carbonate as well as polyethylene glycol sorbitan fatty acid esters.
Auch in der Patentliteratur findet sich die Verwendung von Sprengmitteln. So wird in der deutschen Patentanmeldung DE 938 566 vorgeschlagen, Acetylsalicylsäure vor dem Ver- pressen zunächst in Granulatform zu überführen, schonend, aber vollständig zu trocknen und anschließend mit hochdisperser Kieselsäure zu überziehen. -Anschließend können die mit hochdisperser Kieselsäure abgepuderten Acetylsalicylsäuregranulate mit weiteren Tabletteninhaltsstoffen, welche in pulverförmiger oder granulärer Form vorliegen können, vermischt und zu Tabletten veφreßt werden. Die Trennschicht von hochdisperser Kieselsäure wirkt nicht nur als Isolierschicht und Schutz vor ungewollten Reaktionen, sondern trägt auch zum schnellen Zerfall der Tabletten selbst nach längerer Lagerzeit bei.The use of explosives is also found in the patent literature. In German patent application DE 938 566, for example, it is proposed to convert acetylsalicylic acid into granular form before pressing, to dry it gently but completely and then to coat it with highly disperse silica. Subsequently, the acetylsalicylic acid granules powdered with finely divided silica can be mixed with other tablet ingredients, which may be in powder or granular form, and pressed into tablets. The separating layer of highly disperse silica not only acts as an insulating layer and protection against unwanted reactions, but also contributes to the rapid disintegration of the tablets even after a long storage period.
Die deutsche Patentanmeldung DE 12 28 029 beschreibt die Herstellung von Tabletten, wobei Pulvergemische ohne vorherige Granulation zunächst mit Cellulosepulver und ge-
gebenenfalls hochdisperser Kieselsäure vermischt, gemäß einer bevorzugten Ausfuhrangs- form veimahlen und anschließend veφreßt werden.The German patent application DE 12 28 029 describes the production of tablets, powder mixtures without prior granulation initially containing cellulose powder and mixed if necessary, highly disperse silica, mixed according to a preferred embodiment and then pressed.
Aus der deutschen Patentanmeldung DE 41 21 127 wiederam geht hervor, daß ein besonders guter Hilfsstoff bei der Herstellung von Arzneimitteltabletten Cellulosepartikel aufweist, auf deren Oberfläche ein Kaschiermittel fixiert ist. Der Hilfsstoff wird in möglichst feinteiliger Form eingesetzt; wobei mittlere Partikelgrößen von unterhalb 200 μm als besonders vorteilhaft dargestellt werden. Üblicherweise werden somit die klassischen Ta- blettensprengmittel der ersten genannten Substanzklasse in sehr feinteiliger Form entweder vor dem Veφressen mit den sonstigen Tabletteninhaltsstoffen, die feinteilig oder granulär vorliegen können, vermischt oder die sonstigen Tabletteninhaltsstoffe werden mit dem Tablettensprengmittel überzogen bzw. abgepudert.The German patent application DE 41 21 127 again shows that a particularly good auxiliary in the manufacture of pharmaceutical tablets has cellulose particles on the surface of which a laminating agent is fixed. The excipient is used in the finest possible form; mean particle sizes below 200 μm are shown to be particularly advantageous. Usually, the classic tablet disintegrants of the first class of substances mentioned are mixed in very fine-particle form either before being compressed with the other tablet ingredients, which may be in fine or granular form, or the other tablet ingredients are coated or powdered with the tablet disintegrant.
Auf dem Gebiet der Wasch- oder Reinigungsmittel können gemäß der Lehre des europäischen Patents EP-B-0 523 099 auch die Sprengmittel eingesetzt werden, die von der Arzneimittelherstellung her bekannt sind. Als Sprengmittel genannt werden quellfähige Schichtsilikate wie Bentonite, Naturstoffe und Naturstoff-Derivate auf Stärke- und Cellu- lose-Basis, Alginate und dergleichen, Kartoffelstärke, Methylcellulose und/oder Hydroxy- propyl-cellulose. Diese Sprengmittel können mit den zu veφressenden Granulaten vermischt, aber bereits auch in die zu veφressenden Granulate eingearbeitet werden.In the field of detergents or cleaning agents, according to the teaching of the European patent EP-B-0 523 099, it is also possible to use the disintegrants which are known from the manufacture of pharmaceuticals. Swelling layer silicates such as bentonites, natural substances and natural substance derivatives based on starch and cellulose, alginates and the like, potato starch, methyl cellulose and / or hydroxypropyl cellulose are mentioned as disintegrants. These disintegrants can be mixed with the granules to be milled, but can also be incorporated into the granules to be milled.
Die internationale Patentanmeldung WO-A-96/06156 gibt ebenfalls an, daß der Einbau von Sprengmitteln in Wasch- oder Reinigungsmitteltabletten von Vorteil sein kann. Wiederum werden hier als typische Sprengmittel mücrokristalline Cellulose, Zucker wie Sorbit, aber auch Schichtsilikate, insbesondere feinteilige und quellfähige Schichtsilikate von der .Art der Bentonite und Smektite genannt. Auch zur Gasbildung beitragende Substanzen wie Citronensäure, Bisulfat, Bicarbonat, Carbonat und Percarbonat werden als mögliche Zerfallhilfsmittel aufgeführt.International patent application WO-A-96/06156 also states that the incorporation of disintegrants in detergent or cleaning agent tablets can be advantageous. Again, microcrystalline cellulose, sugars such as sorbitol, but also sheet silicates, in particular finely divided and swellable sheet silicates of the type of bentonites and smectites, are mentioned as typical disintegrants. Substances contributing to gas formation such as citric acid, bisulfate, bicarbonate, carbonate and percarbonate are also listed as possible disintegration aids.
In den europäischen Patentanmeldungen EP-A-0 466485, EP-A-0 522 766, EP-A-0 711 827, EP-A-0 711 828 und EP-A-0 716 144 wird die Herstellung von reinigungsaktiven Tabletten beschrieben, wobei kompaktiertes, partikuläres Material mit einer Partikelgröße zwischen 180 und 2000 μm eingesetzt wird. Die resultierenden Tabletten können sowohl
eine homogene wie auch eine heterogene Struktur aufweisen. Gemäß EP-A-0 522 766 werden zumindest die Teilchen, welche Tenside und Builder enthalten, mit einer Lösung oder Dispersion eines Binders/Zerfallhilfsmittels, insbesondere Polyethylenglykol, umhüllt. Andere Binder/Zerfallhilfsmittel sind wiederam die bereits melirfach beschriebenen und bekannten Sprengmittel, beispielsweise Stärken und Stärkederivate, im Handel erhältliche Cellulose-Derivate wie quervernetzte und modifizierte Cellulose, mi.krokristalline Cellulosefasem, quervernetzte Polyvinylpyrrolidone, Schichtsilikate etc. Auch schwache Säuren wie Citronensäure oder Weinsäure, welche in Zusammenhang mit carbonathaltigen Quellen bei der Kontaktierang mit Wasser zu Spradeleffekten führen und nach der Definition nach Römpp zu der zweiten Klasse der Sprengmittel zählen, können als Coatingmate- rial eingesetzt werden.European patent applications EP-A-0 466485, EP-A-0 522 766, EP-A-0 711 827, EP-A-0 711 828 and EP-A-0 716 144 describe the production of active cleaning tablets, using compact, particulate material with a particle size between 180 and 2000 μm. The resulting tablets can both have a homogeneous as well as a heterogeneous structure. According to EP-A-0 522 766, at least the particles which contain surfactants and builders are coated with a solution or dispersion of a binder / disintegrant, in particular polyethylene glycol. Other binders / disintegrants are again the disintegrants already described and known, for example starches and starch derivatives, commercially available cellulose derivatives such as crosslinked and modified cellulose, microcrystalline cellulose fibers, crosslinked polyvinylpyrrolidones, layered silicates etc. Also weak acids such as citric acid or tartaric acid or tartaric acid or tartaric acid which, in connection with carbonate-containing sources, lead to sprinkling effects when in contact with water and which, according to Römpp's definition, belong to the second class of disintegrants, can be used as a coating material.
Besonders verwiesen wird auf die nicht vorveröffentlichte DE 197 10 254, die Sprengmittel beschreibt, deren Partikelgrößenverteilung (Siebanalyse) derart gestaltet ist, daß maximal 1 Gew.-%, vorzugsweise darunter, an Staubanteilen vorliegen und insgesamt (einschließlich der eventuell vorhandenen Staubanteile) weniger als 10 Gew.-% der Sprengmittelgranulate kleiner als 0,2 mm sind. Vorteilhafterweise weisen dabei mindestens 90 Gew.-% der Sprengmittelgranulate eine Partikelgröße von mindestens 0,2 mm und maximal 3 mm auf. Diese Sprengmittel sind für die vorliegende Erfindung besonders geeignet.Particular reference is made to the unpublished DE 197 10 254, which describes disintegrants whose particle size distribution (sieve analysis) is designed in such a way that a maximum of 1% by weight, preferably less, of dust components is present and overall (including any dust components present) less than 10% by weight of the disintegrant granules are smaller than 0.2 mm. At least 90% by weight of the disintegrant granules advantageously have a particle size of at least 0.2 mm and a maximum of 3 mm. These disintegrants are particularly suitable for the present invention.
Ebenfalls geeignet sind Mittel aus der Gruppe der organischen Säuren, wie z. B. Citronensäure, bzw. eines Gemisches Citronensäure.Bicarbonat und/oder der Cellulosen und Cel- lulosederivate. Ist ein Sprendmittel im Formköφer enthalten, so ist die Auflösezeit des gesamten Formköφers bevorzugt kürzer als die Dauer des Hauptspülgangs einer konventionellen Geschirrspülmaschine, also kürzer als 40 min, besonders bevorzugt kürzer als 30 min, ganz besonders bevorzugt kürzer als 20 min und äußerst bevorzugt kürzer als 10 min.Agents from the group of organic acids, such as. B. citric acid, or a mixture of citric acid. Bicarbonate and / or the celluloses and cellulose derivatives. If a sprinkling agent is contained in the molded article, the dissolution time of the entire molded article is preferably shorter than the duration of the main wash cycle of a conventional dishwasher, i.e. shorter than 40 min, particularly preferably shorter than 30 min, very particularly preferably shorter than 20 min and extremely preferably shorter than 10 min.
Als Material zur Löseverzögerang sind in der Regel Paraffine und/oder Microwachse und/oder der hochmolekularen Polyethylenglycole üblich, die im Stand der Technik ausführlich beschrieben sind. Besonders geeignet für die vorliegende Anmeldung ist der Einsatz von Gemischen, wie er in der nicht vorveröffentlichten Druckschrift DE 197 27 073 erwähnt ist und deren Offenbarung hiermit ausdrücklich in diese Schrift aufgenommen wird.
Ist eine Komponente zur Löseverzögerang enthalten, so ist in einer bevorzugten Ausfuhrungsform die Auflösezeit des gesamten Formköφers in 20 °C kaltem Wasser länger als der Vorspülgang einer handelsüblichen Geschirrspülmaschine, also länger als 5 min, bevorzugt länger als 10 min.Paraffins and / or microwaxes and / or the high molecular weight polyethylene glycols, which are described in detail in the prior art, are generally used as the material for delaying dissolution. The use of mixtures as mentioned in the unpublished publication DE 197 27 073 and the disclosure of which is hereby expressly incorporated into this document is particularly suitable for the present application. If a component for delaying dissolution is included, the dissolution time of the entire molded body in 20 ° C. cold water is longer in a preferred embodiment than the pre-rinse cycle of a commercially available dishwasher, that is to say longer than 5 minutes, preferably longer than 10 minutes.
Allgemeine Darbietungsformen:General forms of presentation:
Für die Raumform des Formköφers eignen sich alle möglichen dreidimensionalen Köφer, wie sie u.a. in den Patentschriften zum Stand der Technik und den Standardwerken der Fachliteratur (z.B.: Riedel, "Die Tablette") aber auch in den Patentschriften des Standes der Technik aufgezählt sind. Der Bereich in dem der Inhaltsstoff (I) enthalten ist, ist ebenfalls nicht an eine spezifische Raumform gebunden. Bevorzugt aus praktischen Gründen ist allerdings eine Ausdehnung in einer Raumrichtung von mehr als 5 mm.All possible three-dimensional bodies are suitable for the spatial shape of the shaped body, such as are listed in the prior art patents and the standard works of the specialist literature (for example: Riedel, "Die Tablette") but also in the prior art patents. The area in which the ingredient (I) is contained is also not tied to a specific spatial form. For practical reasons, however, an expansion in a spatial direction of more than 5 mm is preferred.
Spezifische Darbietungsformen:Specific forms of presentation:
In einer bevorzugten Ausfuhrangsform der Erfindung werden homogene oder heterogene Formköφer bekannter Bauart bereitgestellt.In a preferred embodiment of the invention, homogeneous or heterogeneous molded bodies of known design are provided.
Dazu zählen insbesondere zylinderförmige Tabletten wobei diese Tabletten vorzugsweise einen Durchmesser von 15 bis 60 mm, insbesondere von 30 +/- 10 mm aufweisen. Die Höhe dieser Tabletten beträgt vorzugsweise 5 bis 30 mm und insbesondere 15 bis 28 mm. Besonders günstig haben sich Formköφer mit einem Durchmesser von jeweils 32, 33, 34, 35, 36, 37, 38, und 39 mm erwiesen. Die Höhe beträgt in besonderen Ausgestaltungsformen 24, 25, 26, 27 oder 28 mm.These include in particular cylindrical tablets, these tablets preferably having a diameter of 15 to 60 mm, in particular 30 +/- 10 mm. The height of these tablets is preferably 5 to 30 mm and in particular 15 to 28 mm. Shaped bodies with a diameter of 32, 33, 34, 35, 36, 37, 38 and 39 mm have proven to be particularly favorable. In special designs, the height is 24, 25, 26, 27 or 28 mm.
Aber auch quadratische, rechteckige, trapezförmige, ovale und unregelmäßig geformte GaTundflächen lassen sich bevorzugt einsetzen. Die Kantenlängen liegen dabei bevorzugt zwischen 15 bis 60 mm, insbesondere von 30 +/- 10 mm.Square, rectangular, trapezoidal, oval and irregularly shaped GaTund surfaces can also be used with preference. The edge lengths are preferably between 15 to 60 mm, in particular 30 +/- 10 mm.
Das Gewicht der einzelnen Formköφer, insbesondere der Tabletten, liegt dabei vorzugsweise bei 15 bis 60 g und insbesondere bei 20 bis 40 g pro Formköφer bzw. Tablette; die Stoffdichte der Formköφer bzw. Tabletten weist hingegen üblicherweise Werte oberhalb von 1 kg/dm , vorzugsweise von 1,1 bis 1,4 kg/dm auf.The weight of the individual shaped bodies, in particular the tablets, is preferably 15 to 60 g and in particular 20 to 40 g per shaped body or tablet; the consistency of the molded body or tablets, however, usually has values above 1 kg / dm, preferably from 1.1 to 1.4 kg / dm.
Je nach Art der .Anwendung, des Wasserhärtebereichs oder der Verschmutzung können 1 oder mehrere, beispielsweise 2 bis 4 Formköφer, insbesondere Tabletten, eingesetzt wer-
den. Weitere erfindungsgemäße Formköφer können auch kleinere Durchmesser bzw. Abmessungen, beispielsweise um 10 mm, aufweisen.Depending on the type of application, the water hardness range or the level of contamination, 1 or more, for example 2 to 4, molded articles, in particular tablets, can be used. the. Further shaped bodies according to the invention can also have smaller diameters or dimensions, for example around 10 mm.
Unter einem homogenen Formköφer werden derartige verstanden, in denen die Inhaltsstoffe des Foraiköφers bis auf den Bereich mit Inhaltsstoff (I) in der Weise homogen verteilt sind, daß mit dem bloßen Auge keine unterschiedlichen Inhaltsstoffe und/oder Wirkstoffe wahrzunehmen sind. Dabei kann natürlich der Kornaufbau der eingesetzten Feststoffe noch zu erkennen sein. In einer bevorzugten Ausfuhrangsform der Erfindung ist neben dem Bereich mit dem Inhaltsstoff (I) nur noch ein weiterer Bereich (Phase) vorhanden,A homogeneous shaped body is understood to mean those in which the ingredients of the fora body are homogeneously distributed except for the area with ingredient (I) in such a way that no different ingredients and / or active ingredients are perceptible to the naked eye. The grain structure of the solids used can of course still be recognized. In a preferred embodiment of the invention, in addition to the area with the ingredient (I), only a further area (phase) is present.
Unter heterogenen Formköφern werden dementsprechend solche verstanden, die keine homogene Verteilung der neben dem Inhaltsstoff (I) vorhandenen Inhaltsstoffe aufzuweisen haben. Heterogene Formköφer können in einem einfachen Fall beispielsweise dadurch hergestellt werden, daß die verschiedenen Inhaltsstoffe unterschiedliche Farben aufweisen und/oder eine unterschiedliche Duftkomponente tragen.Heterogeneous shaped bodies are accordingly understood to mean those which do not have a homogeneous distribution of the ingredients present in addition to the ingredient (I). In a simple case, heterogeneous shaped bodies can be produced, for example, by the different ingredients having different colors and / or carrying a different fragrance component.
Ein weiterer Fall der erfindungsgemäß zu den nicht einheitlichen (heterogenen) Formkör- pern zu zählen ist, umfaßt eine Ausgestaltungsform, bei der ein Formköφer veφreßt wird, der neben dem Bereich mit dem Inhaltsstoff (I) mehrere Schichten (Phasen), also mindestens zwei Schichten aufweist. Dabei ist es z. B. möglich, daß diese verschiedenen Schichten unterschiedliche Zerfalls- und Lösegeschwindigkeiten aufweisen und/oder unterschiedliche Inhaltsstoffe tragen. Hieraus können vorteilhafte anwendungstechnische Eigenschaften der Formköφer resultieren. Falls beispielsweise Inhaltsstoffe in den Formköφern enthalten sind, die sich wechselseitig negativ beeinflussen, so ist es möglich diese zu trennen. Soll in einer Maschine eine definierte Abfolge von Reinigungsbedingungen geschaffen werden, so ist es möglich, die eine (oder mehrere) Komponente(n) in einer (oder der) schneller zerfallenden und/oder schneller löslichen Schicht zu integrieren und die andere(n) Komponente(n) in einer (oder der) langsamer zerfallende(n) Schicht einzuarbeiten, so daß eine Komponente mit Vorlaufzeit wirken kann oder bereits abreagiert hat, wenn eine weitere in Lösung geht.Another case, which according to the invention is to be counted as the non-uniform (heterogeneous) molded bodies, comprises an embodiment in which a molded body is pressed which, in addition to the area with the ingredient (I), has several layers (phases), that is to say at least two layers having. It is e.g. B. possible that these different layers have different disintegration and dissolution rates and / or carry different ingredients. This can result in advantageous application properties of the molded body. If, for example, ingredients are contained in the moldings that mutually influence each other, it is possible to separate them. If a defined sequence of cleaning conditions is to be created in a machine, it is possible to integrate one (or more) component (s) in a (or) the more rapidly disintegrating and / or faster dissolving layer and the other (n) component Incorporate into one or more slowly disintegrating layers so that one component can act with a lead time or has already reacted when another goes into solution.
Eine bevorzugte Ausfuhrangsform der Erfindung besteht darin, daß neben dem Bereich mit dem Inhaltsstoff (I) noch zwei weitere Phasen vorhanden sindBesonders günstig ist es, wenn die Volumenverhältnisse der beiden weiteren Phasen zwischen 10:1 und 1 :10, bevorzugt zwischen 5:1 und 1:5, besonders bevorzugt zwischen 2:1 und 1 :2 liegen.
Eine weitere besonders bevorzugte Ausführangsfoim ist dadurch gekennzeichnet, daß drei oder mehr weitere Phasen vorhanden sind.A preferred embodiment of the invention consists in that in addition to the area with the ingredient (I) there are two further phases. It is particularly advantageous if the volume ratios of the two further phases are between 10: 1 and 1:10, preferably between 5: 1 and 1: 5, particularly preferably between 2: 1 and 1: 2. Another particularly preferred embodiment is characterized in that three or more further phases are present.
Der Schichtaufbau der Formköφer kann dabei sowohl stapelartig erfolgen, wobei ein Lösungsvorgang der inneren Schicht(en) an den Kanten des Formköφers bereits dann erfolgt, wenn die äußeren Schichten noch nicht vollständig gelöst oder zerfallen sind; es kann aber auch eine vollständige und/oder teilweise Umhüllung der inneren Schicht(en) durch die weiter außen liegenden Schichten erreicht werden, was zu einer Verhinderang und/oder Verzögerung der frühzeitigen Lösung von Bestandteilen der inneren Schicht(en) fuhrt.The layer structure of the molded body can take place in a stack-like manner, with the inner layer (s) already loosening at the edges of the molded body when the outer layers have not yet been completely detached or disintegrated; however, a complete and / or partial covering of the inner layer (s) can also be achieved by the layers lying further outwards, which leads to a prevention and / or delay in the early dissolution of components of the inner layer (s).
In einer weiteren bevorzugten Ausfuhrangsform der Erfindung besteht eine Tablette aus mindestens drei Schichten, also zwei äußeren und mindestens einer inneren Schicht, wobei mindestens in einer der inneren Schichten ein Peroxy-Bleichmittel enthalten ist, während bei der stapeiförmigen Tablette die beiden Deckschichten und bei der hüllenförmigen Tablette die äußersten Schichten jedoch frei von Peroxy-Bleichmittel sind. Ebenso ist es möglich, Peroxy-Bleichmittel und gegebenenfalls vorhandene Bleichaktivatoren oder Bleichkatalysatoren und/oder Enzyme räumlich in einer Tablette / einem Formköφer voneinander zu trennen. Derartige Ausgestaltungen weisen den Vorteil auf, daß bei den erfindungsgemäßen Formköφeπi keine unerwünschten Wechselwirkungen zu befürchten wären.In a further preferred embodiment of the invention, a tablet consists of at least three layers, that is to say two outer and at least one inner layer, at least one of the inner layers containing a peroxy bleach, while in the case of the tablet in the form of a tablet, the two outer layers and in the case of the shell-like one However, the outermost layers of the tablet are free of peroxy bleach. It is also possible to spatially separate peroxy bleaching agents and any bleach activators or bleach catalysts and / or enzymes present in a tablet / molded article. Such configurations have the advantage that there would be no fear of undesired interactions in the inventive moldings.
Eine weitere günstige und bevorzugte Ausführungsform der Erfindung besteht darin, daß eine der oder die Bleichkomponente, besonders die Chlorkomponente nicht in einer Phase mit der Parfumkomponente zusammen konfektioniert wird. Eine weitere günstige und bevorzugte Ausfuhrangsform der Erfindung besteht darin, daß die Silberschutzkomponente nicht mit einer der oder der Bleichkomponente konfektioniert wird. Eine weitere günstige und bevorzugte Ausführungsform der Erfindung besteht darin, daß eine der oder die Komponente zur Löslichkeitskontrolle zusammen mit dem Bleichaktivator konfektioniert wird. Eine weitere günstige und bevorzugte Ausfuhrangsform der Erfindung besteht darin, daß eine der oder die Komponente zur Löslichkeitskontrolle zusammen mit den Enzymen konfektioniert wird. Eine weitere günstige und bevorzugte Ausführungsform der Erfindung besteht darin, daß eine der oder die Komponente zur Löslichkeitskontrolle zusammen mit dem Bleichmittel konfektioniert wird. Eine weitere günstige und bevorzugte Ausfuhrangsform der Erfindung besteht darin, daß eine der oder die Komponente zur Löslichkeitskon-
trolle zusammen mit der Silberschutzkomponente konfektioniert wird. Eine weitere günstige und bevorzugte Ausfuhrangsform der Erfindung besteht darin, daß eine der oder die Komponente zur Löslichkeitskontrolle zusammen mit mindestens 50 Gew.-%, bevorzugt mehr als 70 Gew.-%, besonders mehr als 90 Gew.-% eines Tensides oder des Gesamtten- sidgemisches konfektioniert wird.Another cheap and preferred embodiment of the invention is that one of the bleaching component or components, especially the chlorine component, is not assembled together with the perfume component in one phase. Another cheap and preferred embodiment of the invention is that the silver protection component is not made up with one or more of the bleaching components. Another cheap and preferred embodiment of the invention is that one of the component or components for solubility control is packaged together with the bleach activator. Another cheap and preferred embodiment of the invention is that one of the component or components for solubility control is packaged together with the enzymes. Another cheap and preferred embodiment of the invention is that one of the component or components for solubility control is packaged together with the bleach. Another cheap and preferred embodiment of the invention is that one of the component or components for solubility trolleys is assembled together with the silver protection component. Another cheap and preferred embodiment of the invention is that one of the component or components for solubility control together with at least 50 wt .-%, preferably more than 70 wt .-%, particularly more than 90 wt .-% of a surfactant or all of them - is mixed.
Die Herstellung der erfindungsgemäßen Mittel erfolgt nach den gängigen Verfahren der Formköφerherstellung.The agents according to the invention are produced by the customary methods of molding production.
Bei einigen Ausführangsformen hat es sich als besonders günstig erwiesen den Bereich mit dem oder den Inhaltsstoffen (I) in Form einer Flüssigkeit (ganz allgemein durch Lösung und/oder Schmelze) gegebenenfalls bei erhöhten Temperaturen in eine vorgefertigte Aussparung der umgebenden Inhaltsstoffe einzufüllen und dann durch übliche technische Maßnahmen diesen Bereich erstarren zu lassen (ganz allgemein durch Trocknung und/oder Kühlung). Dabei hat sich eine Viskosität von mehr als 1500 mPas, bevorzugt mehr als 2000 mPas, besonders bevorzugt zwischen 2000 und 15000 mPas, ganz besonders bevorzugt zwischen 2500 und 7000 mPas und äußerst bevorzugt zwischen 3000 und 4000 mPas besonders bewährt.In some embodiments, it has proven to be particularly advantageous to fill the area with the ingredient (s) (I) in the form of a liquid (generally through solution and / or melt), if necessary at elevated temperatures, into a prefabricated recess in the surrounding ingredients and then through conventional ones technical measures to freeze this area (generally by drying and / or cooling). A viscosity of more than 1500 mPas, preferably more than 2000 mPas, particularly preferably between 2000 and 15000 mPas, very particularly preferably between 2500 and 7000 mPas and extremely preferably between 3000 and 4000 mPas has proven particularly useful.
Besonders wirksam hat sich die Kombination des Wirkstoffes (I) mit schmelzbaren Trägersubstanzen erwiesen. Dazu zählen prinzipiell alle Substanzen mit einem Erstarrungspunkt bei oder besonders oberhalb Raumtemperatur.The combination of the active ingredient (I) with meltable carrier substances has proven particularly effective. In principle, this includes all substances with a solidification point at or especially above room temperature.
Besonders geeignet im Sinne der vorliegenden Erfindung sind dabei nichtionische Tenside (Dehypon® LT 104, Dehypon® LS 54, Dehydol® LS 30, Lutensol® AT 80), Polyethylenglycole mit unterschiedlichen Molekulargewichten (PEG 400, 12000), Seifen (Lorol® C 16), Stearate (Cutina® GMS), aber auch verdickte Natronlauge und schmelzbare Salze, wie Natriumcarbonat - Decahydrat. Die Vor- und Nachteile der einzelnen Inhaltsstoffe sind anhand von Versuchen für den Fachmann nachzuvollziehen. Besonders bevorzugt sind als schmelzbare Komponenten im rahmen der vorliegenden Erfindung Wachse geeignet. Unter "Wachsen" wird eine Reihe natürlicher oder künstlich gewonnener Stoffe verstanden, die in der Regel über 40°C ohne Zersetzung schmelzen und schon wenig oberhalb des Schmelzpunktes verhältnismäßig niedrigviskos und nicht fadenziehend sind. Sie weisen eine stark temperaturabhängige Konsistenz und Löslichkeit auf.
Nach ihrer Herkunft teilt man die Wachse in drei Gruppen ein, die natürlichen Wachse, chemisch modifizierte Wachse und die synthetischen Wachse.Non-ionic surfactants (Dehypon® LT 104, Dehypon® LS 54, Dehydol® LS 30, Lutensol® AT 80), polyethylene glycols with different molecular weights (PEG 400, 12000), soaps (Lorol® C 16 ), Stearates (Cutina® GMS), but also thickened sodium hydroxide solution and meltable salts, such as sodium carbonate - decahydrate. The advantages and disadvantages of the individual ingredients can be understood by the expert on the basis of tests. Waxes are particularly preferred as meltable components in the context of the present invention. "Waxing" is understood to mean a number of natural or artificially obtained substances which generally melt above 40 ° C. without decomposition and which are relatively low-viscosity and not stringy even a little above the melting point. They have a strongly temperature-dependent consistency and solubility. The waxes are divided into three groups according to their origin, natural waxes, chemically modified waxes and synthetic waxes.
Zu den natürlichen Wachsen zählen beispielsweise pflanzliche Wachse wie CandeliUawachs, Carnaubawachs, Japanwachs, Espartograswachs, Korl wachs, Guarumawachs, Reiskeimölwachs, Zuckerrolirwachs, Ouricurywachs, oder Montanwachs, tierische Wachse wie Bienenwachs, Schellackwachs, Walrat, Lanolin (Wollwachs), oder Bürzelfett, Mineralwachse wie Ceresin oder Ozokerit (Erdwachs), oder petrochemische Wachse wie Petrolatum, Paraffinwachse oder Mikrowachse.Natural waxes include, for example, vegetable waxes such as candeliu wax, carnauba wax, japan wax, esparto grass wax, korl wax, guaruma wax, rice germ oil wax, sugar toluene wax, ouricury wax, or montan wax, animal waxes such as beeswax, shellac wax, walnut, lanolin (wool wax), mineral wax, or shearling fat Ceresin or ozokerite (earth wax), or petrochemical waxes such as petrolatum, paraffin waxes or micro waxes.
Zu den chemisch modifizierten Wachsen zählen beispielsweise Hartwachse wie Montanesterwachse, Sassolwachse oder hydrierte Jojobawachse.The chemically modified waxes include hard waxes such as montan ester waxes, Sassol waxes or hydrogenated jojoba waxes.
Unter synthetischen Wachsen werden in der Regel Polyalkylenwachse oder Polyalkylenglycolwachse verstanden.Synthetic waxes are generally understood to mean polyalkylene waxes or polyalkylene glycol waxes.
Ebenfalls zu den Wachsen im Rahmen der vorliegenden Erfindung werden beispielsweise die sogenannten Wachsalkohole gerechnet. Wachsalkohole sind höheimolekulare, wasserunlösliche Fettalkohole mit mehr als 28 bis 40 Kohlenstoffatomen. Die Wachsalkohole kommen beispielsweise in Form von Wachsestern höhermolekularer Fettsäuren (Wachssäuren) als Hauptbestandteil vieler natürlicher Wachse vor. Beispiele für Wachsalkohole sind Lignocerylalkohol (1-Tetracosanol) oder Melissylalkohol. Die schmelzbare Komponente kann gegebenenfalls auch Wollwachsalkohole enthalten, worunter man Triteφen- und Steroidalkohole, beispielsweise Lanolin, versteht. Ebenfalls zumindest anteilig als Bestandteil der schmelzbaren Komponente einsetzbar sind im Rahmen der vorliegenden Erfindung Fettsäureglycerinester oder Fettsäurealkanolamide aber gegebenenfalls auch wasserunlösliche oder nur wenig wasserlösliche Polyalkylenglycolverbindungen.The so-called wax alcohols are also included in the waxes in the context of the present invention, for example. Wax alcohols are high molecular weight, water-insoluble fatty alcohols with more than 28 to 40 carbon atoms. The wax alcohols occur, for example, in the form of wax esters of higher molecular fatty acids (wax acids) as the main component of many natural waxes. Examples of wax alcohols are lignoceryl alcohol (1-tetracosanol) or melissyl alcohol. The fusible component can optionally also contain wool wax alcohols, which means trite phene and steroid alcohols, for example lanolin. In the context of the present invention, fatty acid glycerol esters or fatty acid alkanolamides but also, if appropriate, water-insoluble or only slightly water-soluble polyalkylene glycol compounds can likewise be used at least in part as part of the meltable component.
Bevorzugt enthält die schmelzbare Komponente im überwiegenden .Anteil Parafϊinwachs. Das heißt, daß wenigstens 50 Gew.-% der schmelzbaren Komponente, vorzugsweise mehr, aus
Parafϊinwachs bestehen. Besonders geeignet sind Paraffinwachsgehalte in der Umhüllung von etwa 60 Gew.-%, etwa 70 Gew.-% oder etwa 80 Gew.-%, wobei noch höhere Anteile von beispielsweise mehr als 90 Gew.-% besonders bevorzugt sind. In einer besonderen Ausfuhrangsform der Erfindung besteht die schmelzbare Komponente ausschließlich aus Paraffinwachs.Most of the fusible component preferably contains paraffin wax. That is, at least 50% by weight of the fusible component, preferably more Paraffin wax exist. Paraffin wax contents in the coating of approximately 60% by weight, approximately 70% by weight or approximately 80% by weight are particularly suitable, with even higher proportions of, for example, more than 90% by weight being particularly preferred. In a special embodiment of the invention, the fusible component consists exclusively of paraffin wax.
Paraffinwachse weisen gegenüber den anderen genannten, natürlichen Wachsen im Rahmen der vorliegenden Erfindung den Vorteil auf, daß in einer alkalischen Reinigungsmittelumgebung keine Hydrolyse der Wachse stattfindet (wie sie beispielsweise bei den Wachsestern zu erwarten ist), da Paraffinwachs keine hydrolisierbaren Gruppen enthält.Paraffin waxes have the advantage over the other natural waxes mentioned in the context of the present invention that there is no hydrolysis of the waxes in an alkaline detergent environment (as is to be expected, for example, from the wax esters), since paraffin wax contains no hydrolyzable groups.
Paraffinwachse bestehen hauptsächlich aus Alkanen, sowie niedrigen .Anteilen an Iso- und Cycloalkanen. Das erfindungsgemäß einzusetzende Paraffin weist bevorzugt im wesentlichen keine Bestandteile mit einem Schmelzpunkt von mehr als 70°C, besonders bevorzugt von mehr als 60°C auf. Anteile hochschmelzender Alkane im Paraffin können bei Unterschreitung dieser Schmelztemperatur in der Reinigungsmittelflotte nicht erwünschte Wachsrückstände auf den zu reinigenden Oberflächen oder dem zu reinigenden Gut hinterlassen. Solche Wachsräckstände .führen in der Regel zu einem unschönen Aussehen der gereinigten Oberfläche und sollten daher vermieden werden. Die erfindungsgemäße Umhüllung enthält bevor.zugt mindestens ein Paraffinwachs mit einem Schmelzpunkt von etwa 57°C bis etwa 60°C.Paraffin waxes consist mainly of alkanes, as well as low proportions of iso- and cycloalkanes. The paraffin to be used according to the invention preferably has essentially no constituents with a melting point of more than 70 ° C., particularly preferably of more than 60 ° C. Portions of high-melting alkanes in the paraffin can leave undesired wax residues on the surfaces to be cleaned or the goods to be cleaned if the melting temperature in the detergent solution drops below this. Such wax racks usually lead to an unsightly appearance of the cleaned surface and should therefore be avoided. The coating according to the invention preferably contains at least one paraffin wax with a melting point of about 57 ° C. to about 60 ° C.
Vorzugsweise ist der Gehalt des eingesetzten Paraffmwachses an bei Umgebungstemperatur (in der Regel etwa 10 bis etwa 30°C) festen Alkanen, Isoalkanen und Cycloalkanen möglichst hoch. Je mehr feste Wachsbestandteile in einem Wachs bei Raumtemperatur vorhanden sind, desto brauchbarer ist es im Rahmen der vorliegenden Erfindung. Mit zunehmenden .Anteil an festen Wachsbestandteilen steigt die Belastbarkeit der Umhüllung gegenüber Stößen oder Reibung an anderen Oberflächen an, was zu einem länger anhaltenden Schutz der umhüllten Partikel führt. Hohe .Anteile an Ölen oder flüssigen Wachsbestandteilen können zu einer Schwächung der Umhüllung führen, wodurch Poren geöffnet werden und die mit der
schmlezbaren Komponente konfektionierten Partikel den Eingangs genannten Umgebungseinflüssen ausgesetzt werden.The paraffin wax content of alkanes, isoalkanes and cycloalkanes which are solid at ambient temperature (generally about 10 to about 30 ° C.) is preferably as high as possible. The more solid wax components present in a wax at room temperature, the more useful it is within the scope of the present invention. With increasing proportion of solid wax components, the resilience of the coating to impacts or friction on other surfaces increases, which leads to a longer-lasting protection of the coated particles. High .Share of oils or liquid wax components can weaken the coating, which opens pores and the with the Meltable component assembled particles are exposed to the environmental influences mentioned above.
Bei außergewöhnlich niedrigen Temperaturen, beispielsweise bei Temperaturen unter 0°C, kann die erstarrte schmlezbare Komponente bei Stoßbelastung oder Reibung zerbrechen. Um die Stabilität bei solch niedrigen Temperaturen zu verbessern, können der schmelzbaren Komponente gegebenenfalls Additive zugemischt werden. Geeignete Additive müssen sich vollständig mit dem geschmolzenen Wachs vermischen lassen, dürfen den Schmelzbereich der Umhüllung nicht signifikant ändern, müssen die Elastizität der erstarrten schmelzbaren Komponente bei tiefen Temperaturen verbessern, dürfen die Durchlässigkeit der erstarrten schmelzbaren Komponente gegenüber Wasser oder Feuchtigkeit im allgemeinen nicht erhöhen und dürfen die Viskosität der Schmelze des Umhüllungsmaterials nicht soweit erhöhen, daß eine Verarbeitung erschwert oder gar unmöglich wird. Geeignet Additive, welche die Sprödigkeit einer im wesentlichen aus Paraffin bestehenden Umhüllung bei tiefen Temperaturen herabsetzen, sind beispielsweise EVA-Copolymere, hydrierte Harzsäuremethylester, Polyethylen oder Copolymere aus Ethylacrylat und 2-Ethylhexylacrylat.At unusually low temperatures, for example at temperatures below 0 ° C, the solidified, meltable component can break under impact or friction. In order to improve the stability at such low temperatures, additives can optionally be added to the fusible component. Suitable additives must be able to be mixed completely with the molten wax, must not significantly change the melting range of the coating, must improve the elasticity of the solidified fusible component at low temperatures, must not and must not generally increase the permeability of the solidified fusible component to water or moisture do not increase the viscosity of the melt of the coating material to such an extent that processing becomes difficult or even impossible. Suitable additives which reduce the brittleness of a sheath consisting essentially of paraffin at low temperatures are, for example, EVA copolymers, hydrogenated resin acid methyl ester, polyethylene or copolymers of ethyl acrylate and 2-ethylhexyl acrylate.
Die schmelzbare Komponente kann neben Paraffin als Hauptbestandteil noch eine oder mehrere der oben genannten Wachse oder wachsartigen Substanzen enthalten. Grundsätzlich sollte das die Umhüllung bildende Gemisch so beschaffen sein, daß die Umhüllung wenigstens weitgehend wasserunlöslich ist. Die Löslichkeit in Wasser sollte bei einer Temperatur von etwa 30°C etwa 10 mg 1 nicht übersteigen und vorzugsweise unterhalb 5 mg/1 liegen.In addition to paraffin, the fusible component can also contain one or more of the above-mentioned waxes or wax-like substances as the main constituent. In principle, the mixture forming the cover should be such that the cover is at least largely water-insoluble. The solubility in water should not exceed about 10 mg 1 at a temperature of about 30 ° C. and should preferably be below 5 mg / 1.
Besonders geeignet für die vorliegende Anmeldung ist der Einsatz von Gemischen, wie er in der nicht vorveröffentlichten Druckschrift DE 197 27 073 erwähnt ist und deren Offenbarung hiermit ausdrücklich in diese Schrift aufgenommen wird.The use of mixtures as mentioned in the unpublished publication DE 197 27 073 and the disclosure of which is hereby expressly incorporated into this document is particularly suitable for the present application.
Bei anderen Ausführungsformen werden Teile des Formköφers und/oder Komponenten des Formköφers durch Betrahlung mit Mikrowellen behandelt, um Festigkeit, Feuchtigkeitsgehalt und Löslichkeit positiv zu beeinflußen.
Aber auch ein einfaches Veφressen der Bestandteile ist möglich. Dabei können neben Pulvern und Granulaten auch Microtabs und Formköφer kleinerer Dimensionen als der endgültige Formköφer Verwendung finden.In other embodiments, parts of the molded body and / or components of the molded body are treated by irradiation with microwaves in order to positively influence strength, moisture content and solubility. But a simple pressing of the components is also possible. In addition to powders and granules, microtabs and molded articles of smaller dimensions than the final molded article can also be used.
Spezifische Inhaltsstoffe:Specific ingredients:
Besondere Inhaltsstoffe (I) die im Rahmen der Erfindung genutzt werden; sind die Tenside. Als Tenside kommen prinzipiell alle Tenside in Frage. Bevorzugt sind die nichtionischen Tenside und hier vor allem die schwachschäumenden nichtionischen Tenside, aber auch andere schwachschäumende Tenside kommen in Frage. Besonders bevorzugt sind die alkoxylierten Alkohole, besonders die ethoxylierten und/oder propoxylierten, die Alkyl- polyglycoside und die A'kylpolyglucamide.Special ingredients (I) which are used in the context of the invention; are the surfactants. In principle, all surfactants can be used as surfactants. Preference is given to the nonionic surfactants and in particular the low-foaming nonionic surfactants, but other low-foaming surfactants are also suitable. The alkoxylated alcohols, particularly the ethoxylated and / or propoxylated ones, the alkyl polyglycosides and the alkyl polyglucamides are particularly preferred.
Dabei versteht der Fachmann allgemein unter alkoxylierten Alkoholen die Reaktionsprodukte von Alkylenoxid, bevorzugt Ethylenoxid, mit Alkoholen, bevorzugt im Sinne der vorliegenden Erfindung die längerkettigen Alkohole (Cι0 bis Cig, bevorzugt zwischen C12 und C16, wie z. B. Cn-, Cι2-, Cι -, Cι4-, Cι5-, Cι6- ,Cι7- und Cι8-Alkohole). In der Regel enstehen aus n Molen Ethylenoxid und einem Mol Alkohol, abhängig von den Reaktionsbedingungen ein komplexes Gemisch von Additionsprodukten unterschiedlichen Ethoxy- lierungsgrades. Eine weitere Ausfuhrangsform besteht im Einsatz von Gemischen der Al- kylenoxide bevozugt des Gemisches von Ethylenoxid und Propylenoxid. Auch kann man gewünschtenfalls durch eine abschließende Veretherang mit kurzkettigen Alkylgruppen, wie bevorzugt der Butylgrappe, zur Substanzklasse der "verschlossenen" Alkoholethoxy- laten gelangen, die ebenfalls im Sinne der Erfindung eingesetzt werden kann. Ganz besonders bevorzugt im Sinne der vorliegenden Erfindung sind dabei hochethoxylierte Fettalkohole oder deren Gemische mit endgruppenverschlossenen Fettalkoholethoxylaten.The person skilled in the art generally understands alkoxylated alcohols to mean the reaction products of alkylene oxide, preferably ethylene oxide, with alcohols, preferably in the sense of the present invention the longer-chain alcohols (C 1 -C 1, preferably between C 12 and C 16 , such as Cn-, Cι 2 -, Cι -, Cι 4 -, Cι 5 -, Cι 6 -, Cι 7 - and Cι 8 alcohols). As a rule, n moles of ethylene oxide and one mole of alcohol form a complex mixture of addition products of different degrees of ethoxylation, depending on the reaction conditions. Another embodiment is the use of mixtures of the alkylene oxides, preferably the mixture of ethylene oxide and propylene oxide. If desired, a final etherification with short-chain alkyl groups, such as preferably the butyl group, can also lead to the "closed" alcohol ethoxylate class, which can also be used in the context of the invention. Highly preferred for the purposes of the present invention are highly ethoxylated fatty alcohols or their mixtures with end-capped fatty alcohol ethoxylates.
Besonders bevorzugt sind die hydroxylgrappenhaltigen alkoxylierten Alkohole, wie sie in der EP 300 305 beschrieben sind, deren Offenbarung hier ausdrücklich aufgenommen wird. Dabei stand zunächst nur die Reinigungsleistung der Formköφer im Mittelpunkt der Untersuchungen. Im Laufe der Experimente zeigte sich aber, daß im Vergleich zu herkömmlichen Tensiden, diese Hydroxymischether ein ausgezeichneten Klarspüleffekt zeigen. Die gilt besonders bevorzugt in Gemischen mit anderen nichtionischen Tensiden, wie Dehypon LS 54, und auch in Gemischen mit Dehydol LS 4, aber auch Gemische mit Hydroxymischether und .APG. Unerwartet neben dem überraschenden Klarspüleffekt, war,
daß diese Tensidmischungen bereits in homogener Mischung die Spannungsrißkorossion an Kunststoff entscheidend verringerten.The alkoxylated alcohols containing hydroxyl groups are particularly preferred, as described in EP 300 305, the disclosure of which is expressly incorporated here. Initially, only the cleaning performance of the molded bodies was the focus of the investigations. In the course of the experiments, however, it was found that, compared to conventional surfactants, these hydroxy mixed ethers have an excellent rinse aid effect. This applies particularly preferably in mixtures with other nonionic surfactants, such as Dehypon LS 54, and also in mixtures with Dehydol LS 4, but also in mixtures with hydroxy mixed ether and .APG. In addition to the surprising rinse aid effect, that these surfactant mixtures, even in a homogeneous mixture, decisively reduced the stress corrosion crack on plastic.
Alkylpolyglycoside sind Tenside, die durch die Reaktion von Zuckern und Alkoholen nach den einschlägigen Verfaliren der präparativen organischen Chemie erhalten werden können, wobei es je nach Art der Herstellung zu einem Gemisch monoalkylierter, oligomerer oder polymerer Zucker kommt. Bevorzugte Alkylpolyglykoside können Alkylpolyglucosi- de sein, wobei besonders bevorzugt der Alkohol ein langkettiger Fettalkohol oder ein Gemisch langkettiger Fettalkohole ist und der Oligomerisierangsgrad der Zucker zwischen 1 und 10 ist.Alkyl polyglycosides are surfactants which can be obtained by the reaction of sugars and alcohols according to the relevant procedures in preparative organic chemistry, with a mixture of monoalkylated, oligomeric or polymeric sugars depending on the type of preparation. Preferred alkyl polyglycosides can be alkyl polyglucosides, the alcohol being particularly preferably a long-chain fatty alcohol or a mixture of long-chain fatty alcohols and the degree of oligomerization of the sugars being between 1 and 10.
Fettsäurepolyhydroxylamide (Glucamide) sind acylierte Reakionsprodukte der redu tiven Aminierang eines Zuckers (Glucose) mit Ammoniak, wobei als Acylierangsmittel in der Regel langkettige Fettsäuren, langkettige Fettsäureester oder langkettige Fettsäurechloride genutzt werden. Dabei entstehen sekundäre Amide, wenn man statt mit Ammoniak mit Methylamin oder Ethylamin reduziert, wie z. B. in SÖFW-Journal, 119, (1993), 794-808 beschrieben wird. Bevorzugt benutzt man Kohlenstoffkettenlängen von C6 bis C12 im Fettsäurerest.Fatty acid polyhydroxylamides (glucamides) are acylated reaction products of the reductive amination rank of a sugar (glucose) with ammonia, whereby long-chain fatty acids, long-chain fatty acid esters or long-chain fatty acid chlorides are generally used as acylating agents. Secondary amides are formed when reducing with methylamine or ethylamine instead of with ammonia, such as. B. in SÖFW-Journal, 119, (1993), 794-808. Carbon chain lengths of C 6 to C 12 in the fatty acid residue are preferably used.
Besondere Inhaltsstoffe (I) die im Rahmen der Erfindung genutzt werden, sind Sauerstoffbleichmittel, bevorzugt die Alkalimetallperborate und ihre Hydrate und die Alkalimetall- percarbonate, wobei im Rahmen der Erfindung bevorzugt Natriumperborat, als Mono - oder Tetrahydrat, oder Natriumpercarbonat und deren Hydrate Verwendung finden. Ebenfalls einsetzbar sind die Persulfate.Special ingredients (I) which are used in the context of the invention are oxygen bleaching agents, preferably the alkali metal perborates and their hydrates and the alkali metal percarbonates, sodium perborate, as mono- or tetrahydrate, or sodium percarbonate and their hydrates preferably being used in the context of the invention. The persulphates can also be used.
Typische Sauerstoffbleichmittel sind aber auch die organischen Persäuren. Zu den bevorzugt verwendeten organischen Persäuren, zählt vor allem die ausgezeichnet wirksame Phthalimidoperoxycapronsäure, aber auch alle anderen bekannten Persäuren sind prinzipiell verwendbar.Typical oxygen bleaches are also organic peracids. The organic peracids used with preference include above all the excellently active phthalimidoperoxycaproic acid, but in principle all other known peracids can also be used.
Besondere Inhaltsstoffe (I) die im Rahmen der Erfindung genutzt werden, sind Bleichaktivatoren. Bekannte Bleichaktivatoren sind Verbindungen, die eine oder mehrere N- bzw. O- Acylgrappen enthalten, wie Substanzen aus der Klasse der .Anhydride, der Ester, der Imide und der acylierten Imidazole oder Oxime. Beispiele sind Tetraacetylethylendiamin TAED, Tetraacetylmethylendiamin TAMD und Tetraacetylhexylendiamin T.AHD, aber auch Pen-
taacetylglucose PAG, l,5-Diacetyl-2,2-dioxo-hexahydro-l,3,5-triazin DADHT und Isa- tosäureanhydrid ISA.Special ingredients (I) which are used in the context of the invention are bleach activators. Known bleach activators are compounds which contain one or more N- or O-acyl groups, such as substances from the class of anhydrides, esters, imides and acylated imidazoles or oximes. Examples are tetraacetylethylenediamine TAED, tetraacetylmethylenediamine TAMD and tetraacetylhexylenediamine T.AHD, but also pen- taacetylglucose PAG, l, 5-diacetyl-2,2-dioxo-hexahydro-l, 3,5-triazine DADHT and isatoic anhydride ISA.
Als Bleichaktivatoren können Verbindungen, die unter Perhydrolysebedingungen aliphati- sche Peroxocarbonsäuren mit vorzugsweise 1 bis 10 C- Atomen, insbesondere 2 bis 4 C- Atomen, und/oder gegebenenfalls substituierte Perbenzoesäure ergeben, eingesetzt werden. Geeignet sind Substanzen, die O- und/oder N-Acylgrappen der genannten C-Atomzahl und/oder gegebenenfalls substituierte Benzoylgrappen tragen. Bevorzugt sind mehrfach acylierte Alkylendiamine, insbesondere Tetraacetylethylendiamin (T.AED), acylierte Tria- zinderivate, insbesondere l,5-Diacetyl-2,4-dioxohexahydro-l,3,5-triazin (D.ADHT), acylierte Glykolurile, insbesondere Tetraacetylglykoluril (TAGU), N-Acylimide, insbesondere N-Nonanoylsuccinimid (NOSI), acylierte Phenolsulfonate, insbesondere n-Nonanoyl- oder Isononanoyloxybenzolsulfonat (n- bzw. iso-NOBS), Carbonsäureanhydride, insbesondere Phthalsäureanhydrid, acylierte mehrwertige Alkohole, insbesondere Triacetin, Ethylengly- koldiacetat, 2,5-Diacetoxy-2,5-dihydrofuran, n-Methyl-Moφholinium-Acetonitril- Methylsulfat (MMA), und die aus den deutschen Patentanmeldungen DE 196 16 693 und DE 196 16 767 bekannten Enolester sowie acetyliertes Sorbitol und Mannitol beziehungsweise deren in der europäischen Patentanmeldung EP 0 525 239 beschriebene Mischungen (SORM.AN), acylierte Zuckerderivate, insbesondere Pentaacetylglukose (PAG), Penta- acetylfruktose, Tetraacetylxylose und Octaacetyllactose sowie acetyliertes, gegebenenfalls N-alkyliertes Glucamin und Gluconolacton, und/oder N-acylierte Lactame, beispielsweise N-Benzoylcaprolactam, die aus den internationalen Patentanmeldungen WO 94/27970, WO 94/28102, WO 94/28103, WO 95/00626, WO 95/14759 und WO 95/17498 bekannt sind. Die aus der deutschen Patentanmeldung DE 196 16 769 bekannten hydrophil substituierten Acylacetale und die in der deutschen Patentanmeldung DE 196 16 770 sowie der internationalen Patentanmeldung WO 95/14075 beschriebenen Acyllactame werden ebenfalls bevorzugt eingesetzt. Auch die aus der deutschen Patentanmeldung DE 44 43 177 bekannten Kombinationen konventioneller Bleichaktivatoren können eingesetzt werden. Derartige Bleichaktivatoren sind im üblichen Mengenbereich, vorzugsweise in Mengen von 1 Gew.-% bis 10 Gew.-%, insbesondere 2 Gew.-% bis 8 Gew.-%, bezogen auf gesamtes Mittel, enthalten.Compounds which, under perhydrolysis conditions, give aliphatic peroxocarboxylic acids with preferably 1 to 10 C atoms, in particular 2 to 4 C atoms, and / or optionally substituted perbenzoic acid can be used as bleach activators. Suitable are substances which carry O- and / or N-acyl groups of the stated number of carbon atoms and / or optionally substituted benzoyl groups. Multi-acylated alkylenediamines, in particular tetraacetylethylenediamine (T.AED), acylated triazine derivatives, in particular l, 5-diacetyl-2,4-dioxohexahydro-l, 3,5-triazine (D.ADHT), acylated glycolurils, in particular tetraacetylglycoluril, are preferred (TAGU), N-acylimides, especially N-nonanoylsuccinimide (NOSI), acylated phenol sulfonates, especially n-nonanoyl- or isononanoyloxybenzenesulfonate (n- or iso-NOBS), carboxylic acid anhydrides, especially phthalic anhydride, especially acylated trihydric alcohols, acylated polyhydric alcohols, koldiacetate, 2,5-diacetoxy-2,5-dihydrofuran, n-methyl-Moφholinium-acetonitrile-methyl sulfate (MMA), and the enol esters known from German patent applications DE 196 16 693 and DE 196 16 767 as well as acetylated sorbitol and mannitol respectively their mixtures described in European patent application EP 0 525 239 (SORM.AN), acylated sugar derivatives, in particular pentaacetylglucose (PAG), pentaacetylfructose, tetraacetylxylose and the like d Octaacetyllactose and acetylated, optionally N-alkylated glucamine and gluconolactone, and / or N-acylated lactams, for example N-benzoylcaprolactam, which are known from international patent applications WO 94/27970, WO 94/28102, WO 94/28103, WO 95/00626 , WO 95/14759 and WO 95/17498 are known. The hydrophilically substituted acylacetals known from German patent application DE 196 16 769 and the acyl lactams described in German patent application DE 196 16 770 and international patent application WO 95/14075 are also preferably used. The combinations of conventional bleach activators known from German patent application DE 44 43 177 can also be used. Bleach activators of this type are present in the customary quantitative range, preferably in amounts of 1% by weight to 10% by weight, in particular 2% by weight to 8% by weight, based on the total agent.
Zusätzlich zu den oben aufgefülirten konventionellen Bleichaktivatoren oder an deren Stelle können auch die aus den europäischen Patentschriften EP 0 446 982 und
EP 0 453 003 bekannten Sulfonimine und/oder bleichverstärkende Übergangsmetallsalze beziehungsweise Übergangsmetallkomplexe als sogenannte Bleichkatalysatoren enthalten sein. Zu den in Frage kommenden Übergangsmetallverbindungen gehören insbesondere die aus der deutschen Patentanmeldung DE 195 29 905 bekannten Mangan-, Eisen-, Cobalt-, Ruthenium- oder Molybdän-Salenkomplexe und deren aus der deutschen Patentanmeldung DE 196 20 267 bekannte N-.Analogverbindungen, die aus der deutschen Patentanmeldung DE 195 36 082 bekannten Mangan-, Eisen-, Cobalt-, Ruthenium- oder Molybdän-Carbonylkomplexe, die in der deutschen Patentanmeldung DE 196 05 688 beschriebenen Mangan-, Eisen-, Cobalt-, Ruthenium-, Molybdän-, Titan-, Vanadium- und Kupfer-Komplexe mit stickstoffhaltigen Tripod-Liganden, die aus der deutschen Patentanmeldung DE 196 20 411 bekannten Cobalt-, Eisen-, Kupfer- und Ruthenium- Amminkomplexe, die in der deutschen Patentanmeldung DE 44 16 438 beschriebenen M.angan-, Kupfer- und Cobalt-Komplexe, die in der europäischen Patentanmeldung EP 0 272 030 beschriebenen Cobalt-Komplexe, die aus der europäischen Patentanmeldung EP 0 693 550 bekannten Mangan-Komplexe, die aus der europäischen Patentschrift EP 0 392 592 bekannten Mangan-, Eisen-, Cobalt- und Kupfer-Komplexe und/oder die in der europäischen Patentschrift EP 0443 651 oder den europäischen Patentanmeldungen EP 0 458 397, EP 0 458 398, EP 0 549 271, EP 0 549 272, EP 0 544 490 und EP 0 544 519 beschriebenen Mangan-Komplexe. Kombinationen aus Bleichaktivatoren und Übergangsmetall-Bleichkatalysatoren sind beispielsweise aus der deutschen Patentanmeldung DE 196 13 103 und der internationalen Patentanmeldung WO 95/27775 bekannt. Bevorzugt werden Bleichaktivatoren aus der Gruppe der mehrfach acylierte Al- kylendiamine, insbesondere Tetraacetylethylendiamin (TAED), N-Acylimide, insbesondere N-Nonanoylsuccinimid (NOSI), acylierte Phenolsulfonate, insbesondere n-Nonanoyl- oder Isononanoyloxybenzolsulfonat (n- bzw. iso-NOBS), MMA, vorzugsweise in Mengen bis 10 Gew.-%, insbesondere 0J Gew.-% bis 8 Gew.-%, besonders 2 bis 8 Gew.-% und besonders bevorzugt 2 bis 6 Gew.-% bezogen auf das gesamte Mittel, eingesetzt.In addition to the conventional bleach activators listed above or in their place, those from European patent specifications EP 0 446 982 and Known EP 0 453 003 sulfonimines and / or bleach-enhancing transition metal salts or transition metal complexes may be included as so-called bleaching catalysts. The transition metal compounds in question include in particular the manganese, iron, cobalt, ruthenium or molybdenum salen complexes known from German patent application DE 195 29 905 and their N-analogue compounds known from German patent application DE 196 20 267 Manganese, iron, cobalt, ruthenium or molybdenum carbonyl complexes known from German patent application DE 195 36 082, the manganese, iron, cobalt, ruthenium, molybdenum, Titanium, vanadium and copper complexes with nitrogen-containing tripod ligands, the cobalt, iron, copper and ruthenium amine complexes known from German patent application DE 196 20 411, the M. described in German patent application DE 44 16 438 angan, copper and cobalt complexes, the cobalt complexes described in European patent application EP 0 272 030, the manganese com. known from European patent application EP 0 693 550 plexes, the manganese, iron, cobalt and copper complexes known from European patent EP 0 392 592 and / or those described in European patent EP 0443 651 or European patent applications EP 0 458 397, EP 0 458 398, EP 0 549 271, EP 0 549 272, EP 0 544 490 and EP 0 544 519 described manganese complexes. Combinations of bleach activators and transition metal bleach catalysts are known, for example, from German patent application DE 196 13 103 and international patent application WO 95/27775. Bleach activators from the group of multi-acylated alkylenediamines, in particular tetraacetylethylene diamine (TAED), N-acylimides, in particular N-nonanoylsuccinimide (NOSI), acylated phenolsulfonates, in particular n-nonanoyl- or isononanoyloxybenzenesulfonate (NOBS) or isobenzene sulfonate (N-) iso MMA, preferably in amounts of up to 10% by weight, in particular 0J% by weight to 8% by weight, particularly 2 to 8% by weight and particularly preferably 2 to 6% by weight, based on the total composition, used.
Bleichverstärkende Übergangsmetallkomplexe, insbesondere mit den Zentralatomen Mn, Fe, Co, Cu, Mo, V, Ti und/oder Ru, bevorzugt ausgewählt aus der Gruppe der Mangan und/oder Cobaltsalze und/oder -komplexe, besonders bevorzugt der Cobalt(ammin)- Komplexe, der Cobalt(acetat)-Komplexe, der Cobalt(Carbonyl)-Komplexe, der Chloride des Cobalts oder Mangans, des Mangansulfatswerden in üblichen Mengen, vorzugsweise
in einer Menge bis zu 5 Gew.-%, insbesondere von 0,0025 Gew.-% bis 1 Gew.-% und besonders bevorzugt von 0,01 Gew.-% bis 0,25 Gew.-%, jeweils bezogen auf das gesamte Mittel, eingesetzt. Aber in spezielle Fällen kann auch mehr Bleichaktivator eingesetzt werden.Bleach-boosting transition metal complexes, in particular with the central atoms Mn, Fe, Co, Cu, Mo, V, Ti and / or Ru, preferably selected from the group consisting of manganese and / or cobalt salts and / or complexes, particularly preferably cobalt (ammin) - Complexes, the cobalt (acetate) complexes, the cobalt (carbonyl) complexes, the chlorides of cobalt or manganese, of manganese sulfate are used in conventional amounts, preferably in an amount up to 5% by weight, in particular from 0.0025% by weight to 1% by weight and particularly preferably from 0.01% by weight to 0.25% by weight, in each case based on the entire funds. But in special cases, more bleach activator can be used.
Erfindungsgemäße Geschirrspülmittel können als Inhaltsstoff (I) zum Schütze des Spülgutes oder der Maschine Korrosionsinhibitoren enthalten, wobei besonders Silberschutzmittel im Bereich des maschinellen Geschirrspülens eine besondere Bedeutung haben. Einsetzbar sind die bekannten Subsatnzen des Standes der Technik, wie z. B. in der DE 43 25 922, der DE 41 28 672 oder der DE 43 38 724 beschrieben. Allgemein können vor allem Silberschutzmittel ausgewählt aus der Gruppe der Triazole, der Benzotriazole, der Bisben- zotriazole, der Aminotriazole, der Alkylaminotriazole und der Übergangsmetallsalze oder - komplexe eingesetzt werden. Besonders bevorzugt zu verwenden sind Benzotriazol und/oder Alkylaminotriazol. Man findet in Remigerformulierangen darüberhinaus häufig aktivchlorhaltige Mittel, die das Korrodieren der Silberoberfläche deutlich vermindern können. In chlorfreien Reinigern werden gemäß der obigen Schriften besonders sauerstoff- und stickstoffhaltige organische redoxaktive Verbindungen, wie zwei- und dreiwertige Phenole, z. B. Hydrochinon, Brenzkatechin, Hydroxyhydrochinon, Gallussäure, Phloro- glucin, Pyrogallol bzw. Derivate dieser Verbindungsklassen. Auch salz- und komplexartige anorganische Verbindungen, wie Salze der Metalle Mn, Ti, Zr, Hf, V, Co und Ce finden häufig Verwendung. Bevorzugt sind hierbei die Übergangsmetallsalze, die ausgewählt sind aus der Gruppe der Mangan und/oder Cobaltsalze und/oder -komplexe, besonders bevorzugt der Cobalt(ammin)-Komplexe, der Cobalt(acetat)-Komplexe, der Cobalt-(Carbonyl)- Komplexe, der Chloride des Cobalts oder Mangans und des Mangansulfats. Ebenfalls können Zinkverbindungen zur Verhinderang der Korrosion am Spülgut eingesetzt werden.Dishwashing detergents according to the invention can contain corrosion inhibitors as ingredient (I) to protect the items to be washed or the machine, silver protection agents in particular being particularly important in the field of automatic dishwashing. The known subsets of the prior art, such as. B. described in DE 43 25 922, DE 41 28 672 or DE 43 38 724. In general, silver protection agents selected from the group consisting of the triazoles, the benzotriazoles, the bisbenzotriazoles, the aminotriazoles, the alkylaminotriazoles and the transition metal salts or complexes can be used. Benzotriazole and / or alkylaminotriazole are particularly preferably to be used. Agents containing active chlorine, which can significantly reduce the corroding of the silver surface, are also frequently found in Remiger formulation oranges. In chlorine-free cleaners, especially oxygen and nitrogen-containing organic redox-active compounds, such as di- and trihydric phenols, e.g. B. hydroquinone, pyrocatechol, hydroxyhydroquinone, gallic acid, phloroglucin, pyrogallol or derivatives of these classes of compounds. Salt-like and complex-like inorganic compounds, such as salts of the metals Mn, Ti, Zr, Hf, V, Co and Ce, are also frequently used. Preferred here are the transition metal salts which are selected from the group consisting of manganese and / or cobalt salts and / or complexes, particularly preferably the cobalt (amine) complexes, the cobalt (acetate) complexes, the cobalt (carbonyl) complexes , the chlorides of cobalt or manganese and manganese sulfate. Zinc compounds can also be used to prevent corrosion on the wash ware.
Besondere Inhaltsstoffe (I) die im Rahmen der Erfindung genutzt werden, sind Substanzen, die das Wiederanschmutzen von Oberflächen verhinden und/oder die Schmutzablösung nach einmaliger Anwendung erleichtern (sogenannte " Soil-Release- Verbindungen").Special ingredients (I) which are used in the context of the invention are substances which prevent the re-soiling of surfaces and / or facilitate the detachment of dirt after a single application (so-called “soil release compounds”).
Zu den erfmdungsgemäß verwendeten Soil-Release Verbindungen zählen alle im Stand der Technik bekannten Verbindungen. Besonders geeignet sind kationische Polymere, wie sie z. B. aus den folgenden Druckschriften bekannt sind:
In der EP-A-0 167 382, EP-A-0 342 997 sowie DE-OS-26 16 404 werden Reinigungsmitteln kationische Polymere zugesetzen, um so eine möglichst streifenfreie Reinigung der Oberflächen zu erreichen.The soil release compounds used according to the invention include all compounds known in the prior art. Cationic polymers such as those used for. B. are known from the following publications: In EP-A-0 167 382, EP-A-0 342 997 and DE-OS-26 16 404 cleaning agents are added cationic polymers in order to achieve a streak-free cleaning of the surfaces.
In der EP-A-0 167 382 werden flüssige Reinigungsmittelzusammensetzungen beschrieben, die als Verdickungsmittel kationische Polymere enthalten können. Als besonders geeignete kationische Polymere werden Hydroxypropyltrimethylammonium-Guar; Copolymere von .Aminoethylmethacrylat und Acrylamid sowie Copolymere von Dimethyldiallyl- ammoniumchlorid und Acrylamid beschrieben.EP-A-0 167 382 describes liquid detergent compositions which can contain cationic polymers as thickeners. Hydroxypropyltrimethylammonium guar; Copolymers of .Aminoethyl methacrylate and acrylamide and copolymers of dimethyldiallylammonium chloride and acrylamide are described.
In der EP-A-0 342 997 werden Allzweckreiniger beschrieben, die kationische Polymere enthalten können, wobei insbesondere Polymere mit Imino-Grappen eingesetzt werden.EP-A-0 342 997 describes all-purpose cleaners which can contain cationic polymers, in particular polymers with imino grapples being used.
In der DE-OS-26 16 404 werden Reinigungsmittel für Glas beschrieben, die kationische Cellulosederivate enthalten. Der Zusatz der kationischen Cellulosederivate in den Mitteln ein besseres Ablaufen des Wassers, um streifenfrei gereinigtes Glas zu erhalten.DE-OS-26 16 404 describes cleaning agents for glass which contain cationic cellulose derivatives. The addition of the cationic cellulose derivatives in the agents a better drainage of the water in order to obtain streak-free cleaned glass.
In der EP-A-0 467 472 werden z. B. Reinigungsmittel für harte Oberflächen beschrieben, die als Soil-Release-Polymere kationische Homo- und/oder Copolymere enthalten. Diese Polymere besitzen als Monomereinheiten quaternisierte .Ammoniumalkyl- methacrylatgrappen. Diese Verbindungen werden eingesetzt, um die Oberflächen derart auszustatten, daß beim nächsten Reinigungsvorgang sich die .Anschmutzungen leichter ablösen lassen.In EP-A-0 467 472 e.g. B. cleaning agents for hard surfaces are described which contain cationic homo- and / or copolymers as soil-release polymers. These polymers have quaternized ammonium alkyl methacrylate groups as monomer units. These connections are used to equip the surfaces in such a way that the soiling can be removed more easily during the next cleaning process.
Besonders bevorzugt sind die kationischen Polymeren ausgewählt aus kationischen Polymerisaten von Copolymeren von Monomeren wie Trialkylammoniumalkyl(meth)acrylat bzw. -acrylamid; Dialkyldiallyldiammoniumsalze; polymeranalogen Umsetzungsprodukten von Ethern oder Estern von Polysacchariden mit .Ammoniumseitengrappen, insbesondere Guar-, Cellulose- und Stärkederivate; Polyaddukte von Ethylenoxid mit .Ammonium- grappen; quatemäre Ethyleniminpolymere und Polyester und Polyamide mit quaternären Seitengrappen als Soil-Release- Verbindungen.The cationic polymers are particularly preferably selected from cationic polymers of copolymers of monomers such as trialkylammonium alkyl (meth) acrylate or acrylamide; Dialkyldiallyldiammonium salts; polymer-analogous reaction products of ethers or esters of polysaccharides with ammonium side groups, in particular guar, cellulose and starch derivatives; Polyadducts of ethylene oxide with .ammonium grapples; quaternary ethylene imine polymers and polyesters and polyamides with quaternary side groups as soil release compounds.
Außergewöhnlich bevorzugt im Rahmen dieser .Anmeldung sind auch natürliche Polyuron- säuren und verwandte Substanzen, sowie Polyampholyte und hydrophobierte Polyampho- lyte, bzw. Gemische dieser Substanzen.
Erfndungsgemäß können dem Reinigungsmittel zwischen 0 und 5 Gew.-% Enzyme bezogen auf die gesamte Zubereitung zugesetzt werden, um die Leistung der Reinigungsmittel zu steigern oder unter milderen Bedingungen die Reinigungsleistung in gleicher Qualität zu gewährleisten. Zu den am häufigsten verwendeteten Enzymen gehören Lipasen, Amyla- sen, Cellulasen und Proteasen. Bevorzugte Proteasen sind z. B. BL.AP®140 der Fa. Bio- zym, Optimase®-M-440 und Opticlean®-M-250 der Fa. Solvay Enzymes; Maxacal®CX und Maxapem® oder Esperase® der Fa. Gist Brocades oder auch Savinase® der Fa. Novo. Besonders geeignete Cellulasen und Lipasen sind Celluzym® 0,7 T und Lipolase® 30 T der Fa. Novo Nordisk. Besondere Verwendung als Amylasen finden Duramyl® und Ter- mamyl® 60 T, und Termamyl® 90 T der Fa. Novo, Amylase-LT® der Fa. Solvay Enzymes oder Maxamyl® P5000 der Fa. Gist Brocades. Auch andere Enzyme können verwendet werden.In the context of this application, natural polyuronic acids and related substances, as well as polyampholytes and hydrophobicized polyampholytes, or mixtures of these substances, are also exceptionally preferred. According to the invention, between 0 and 5% by weight of enzymes based on the entire preparation can be added to the cleaning agent in order to increase the performance of the cleaning agents or to guarantee the same quality of cleaning performance under milder conditions. The most commonly used enzymes include lipases, amylases, cellulases and proteases. Preferred proteases are e.g. B. BL.AP®140 from Biozym, Optimase®-M-440 and Opticlean®-M-250 from Solvay Enzymes; Maxacal®CX and Maxapem® or Esperase® from Gist Brocades or Savinase® from Novo. Particularly suitable cellulases and lipases are Celluzym® 0.7 T and Lipolase® 30 T from Novo Nordisk. Duramyl® and Termamyl® 60 T, and Termamyl® 90 T from Novo, Amylase-LT® from Solvay Enzymes or Maxamyl® P5000 from Gist Brocades find particular use as amylases. Other enzymes can also be used.
Weitere Inhaltsstoffe:Other ingredients:
In den erfindungsgemäßen Formköφerτι können alle vorstehend beschriebenen Inhaltsstoffe (I) auch die Funktion von weiteren Inhaltsstoffen einnehmen, sollte die Bedingung des erfindungsgemäßen Bereiches von anderen Inhaltsstoffen erfüllt werden.In the moldings according to the invention, all of the ingredients (I) described above can also take on the function of other ingredients if the condition of the inventive area is met by other ingredients.
In den erfindungsgemäßen Reinigungsmitteln können wasserlösliche und wasserunlösliche Builder vor allem zum Binden von Calcium und Magnesium eingesetzt werden. Dabei sind wasserlösliche Builder bevorzugt, da sie auf Geschirr und harten Oberflächen in der Regel weniger dazu tendieren unlösliche Rückstände zu bilden. Übliche Builder, die im Rahmen der Erfindung zwischen 10 und 90 Gew.-% bezogen auf die gesamte Zubereitung zugegen sein können, sind die niedermolekularen Polycarbonsäuren und ihre Salze, die homopoly- meren und copolymeren Polycarbonsäuren und ihre Salze, die Carbonate, Phosphate und Silikate. Zu wasserunlöslichen Buildern zählen die Zeolithe, die ebenfalls verwendet werden können, ebenso wie Mischungen der vorgenannten Buildersubstanzen.In the cleaning agents according to the invention, water-soluble and water-insoluble builders can be used especially for binding calcium and magnesium. Water-soluble builders are preferred because they generally have less tendency to form insoluble residues on dishes and hard surfaces. Customary builders, which can be present in the scope of the invention between 10 and 90% by weight, based on the entire preparation, are the low molecular weight polycarboxylic acids and their salts, the homopolymeric and copolymeric polycarboxylic acids and their salts, the carbonates, phosphates and silicates . Water-insoluble builders include the zeolites, which can also be used, as well as mixtures of the abovementioned builder substances.
Bevorzugt werden Trinatriumcitrat und/oder Pentanatriumtripolyphosphat und/oder Natri- umcarbonat und/oder Natriumbicarbonat und/oder Gluconate und/oder silikatische Builder aus der Klasse der Disilikate und/oder Metasilikate eingesetzt.Trisodium citrate and / or pentasodium tripolyphosphate and / or sodium carbonate and / or sodium bicarbonate and / or gluconates and / or silicate builders from the class of disilicate and / or metasilicate are preferably used.
Als weitere Bestandteile können Alkaliträger zugegen sein. Als Alkaliträger gelten Alka- limetallhydroxide, Alkalimetallcarbonate, Alkalimetallhydrogencarbonate, Alkalimetall-
sesquicarbonate, Alkalisilikate, Alkalimetasilikate, und Mischungen der vorgenannten Stoffe, wobei im Sinne dieser Erfindung bevorzugt die Alkalicarbonate, insbesondere Na- triumcarbonat, Natriumhydrogencarbonat oder Natriumsesquicarbonat eingesetzt werden.Alkali carriers can be present as further constituents. Alkali metal hydroxides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal sesquicarbonates, alkali silicates, alkali metasilicates, and mixtures of the abovementioned substances, the alkali carbonates, in particular sodium carbonate, sodium hydrogen carbonate or sodium sesquicarbonate, preferably being used for the purposes of this invention.
Besonders bevorzugt ist ein Buildersystem enthaltend eine Mischung aus Tripolyphosphat und Natriumcarbonat.A builder system containing a mixture of tripolyphosphate and sodium carbonate is particularly preferred.
Ebenfalls besonders bevorzugt ist ein Buildersystem enthaltend eine Mischung aus Tripolyphosphat und Natriumcarbonat und Natriumdisilikat.A builder system containing a mixture of tripolyphosphate and sodium carbonate and sodium disilicate is also particularly preferred.
Die Bereiche des Formköφers können gefärbt sein. Besonders bevorzugt ist es dabei, wenn in dem Formköφer eine oder mehrere oder alle Bereiche des Formköφers unterschiedlich gefärbt sind. In einer speziellen Ausgestaltung des Formköφers ist die Farbe Rot. In einer anderen speziellen Ausgestaltung des Formköφers ist die Farbe Grün. In einer anderen speziellen Ausgestaltung des Formköφers ist die Farbe Gelb. In einer anderen speziellen Ausgestaltung des Formköφers ist die Farbe eine Mischung verschiedener Farben.The areas of the molded body can be colored. It is particularly preferred if one or more or all areas of the molded body are colored differently in the molded body. In one special embodiment of the molded body, the color is red. In another special embodiment of the molded body, the color is green. In another special embodiment of the molded body, the color is yellow. In another special embodiment of the molded body, the color is a mixture of different colors.
Die Lagerstabilität des Formköφers ist besonders wichtig. Dabei ist erfindungsgemäß besonders bevorzugt, wenn die Gewichtszunahme des Bereichs dem Inhaltsstoffes (I) bei Lagerung unter normalen Haushaltsbedingungen, d. h. zwischen 15 und 30 °C und zwischen 5 und 55 % Luftfeuchtigkeit, bevorzugt 15 und 35 % Luftfeuchtigkeit für die Dauer von 30 Tagen, bevorzugt 60 Tagen, besonders bevorzugt 90 Tagen nicht mehr als 50 Gew.-%, bevorzugt nicht mehr als 40 Gew.-%, ganz besonders bevorzugt nicht mehr als 30 Gew.-%, außerordentlich bevorzugt nicht mehr als 20 Gew.-% und äußerst bevorzugt nicht mehr als 10 Gew.-% günstigstenfalls nicht mehr als 5 Gew.-% beträgt.The storage stability of the molded body is particularly important. It is particularly preferred according to the invention if the weight increase in the area of the ingredient (I) when stored under normal household conditions, ie. H. between 15 and 30 ° C. and between 5 and 55% atmospheric humidity, preferably 15 and 35% atmospheric humidity for a period of 30 days, preferably 60 days, particularly preferably 90 days, not more than 50% by weight, preferably not more than 40% %, very particularly preferably not more than 30% by weight, extremely preferably not more than 20% by weight and extremely preferably not more than 10% by weight, at best not more than 5% by weight.
Dabei ist erfindungsgemäß außerdem besonders bevorzugt, wenn der Verlust an Aktivsubstanz des Inhaltsstoffes (I) bei Lagerang unter normalen Haushaltsbedingungen, d. h. zwischen 15 und 30 °C und zwischen 5 und 55 % Luftfeuchtigkeit, bevorzugt 15 und 35 % Luftfeuchtigkeit für die Dauer von 30 Tagen, bevorzugt 60 Tagen, besonders bevorzugt 90 Tagen nicht mehr als 50 Gew.-%, bevorzugt nicht mehr als 40 Gew.-%, ganz besonders bevorzugt nicht mehr als 30 Gew.-%, außerordentlich bevorzugt nicht mehr als 20 Gew.-% und äußerst bevorzugt nicht mehr als 10 Gew.-% günstigstenfalls nicht mehr als 5 Gew.-% beträgt.
Dabei ist erfindungsgemäß außerdem besonders bevorzugt, wenn das Absoφtionsmaxi- mum einer 1% igen Lösung eines gefärbten Bereichs oder einer gefärbten Komponente bei Lagerung unter normalen Haushaltsbedingungen, d. h. zwischen 15 und 30 °C und zwischen 5 und 55 % Luftfeuchtigkeit, bevorzugt 15 und 35 % Luftfeuchtigkeit für die Dauer von 30 Tagen, bevorzugt 60 Tagen, besonders bevorzugt 90 Tagen nicht mehr als 100 Wellenzahlen, bevorzugt nicht mehr als 50 Wellenzahlen, ganz besonders bevorzugt nicht mehr als 30 Wellenzahlen, außerordentlich bevorzugt nicht mehr als 20 Wellenzahlen und äußerst bevorzugt nicht mehr als 10 Wellenzahlen günstigstenfalls nicht mehr als 5 Wellenzahlen beträgt.It is also particularly preferred according to the invention if the loss of active substance of the ingredient (I) when stored under normal household conditions, ie between 15 and 30 ° C. and between 5 and 55% atmospheric humidity, preferably 15 and 35% atmospheric humidity for a period of 30 days , preferably 60 days, particularly preferably 90 days not more than 50% by weight, preferably not more than 40% by weight, very particularly preferably not more than 30% by weight, extremely preferably not more than 20% by weight and most preferably not more than 10% by weight, at best not more than 5% by weight. It is also particularly preferred according to the invention if the absorption maximum of a 1% solution of a colored area or a colored component during storage under normal household conditions, ie between 15 and 30 ° C. and between 5 and 55% atmospheric humidity, preferably 15 and 35% Humidity for a period of 30 days, preferably 60 days, particularly preferably 90 days, not more than 100 wave numbers, preferably not more than 50 wave numbers, very particularly preferably not more than 30 wave numbers, extremely preferably not more than 20 wave numbers and extremely preferably not more than 10 wavenumbers, at best not more than 5 wavenumbers.
Wie bereits vorstehend erwähnt, zeigen insbesondere Hydroxymischether als Bestandteil aus der Gruppe der Tenside herausragende Klarspüleffekte und mindern die Spannungsriß- korrosion an Kunststoffen. Weiterhin besitzen sie die Vorteilhafte Eigenschaft, daß ihr Netzverhalten über den gesamten üblichen Temperaturbereich hinweg konstant ist. Der Einsatz der genannten Stoffe als Klarspülkomponente in maschinellen Geschirrspülmitteln ist im Stand der Technik bislang nicht beschrieben. Bislang sind lediglich reine „Reinigungsmittel" bzw. reine „Klarspülmittel" für das maschinelle Geschirrspülen offenbart. Eine Kombination dieser zwei Funktionen in einem Mittel, wie sie die vorliegende Erfindung durch Inkoφoration eines Bestandteils aus der Gruppe der Tenside in eine Formkör- perregion, die nicht mehr als 40 Prozent des Gesamt-Formköφervolumens ausmacht, bereitstellt, ist neu. Ein weiterer gegenstand der vorliegenden Erfindung ist daher einerseits die Verwendung von Hydroxymischethern und/oder Gemischen von Hydroxymischethern und nichtionischen Tensiden als Klarspülkomponente in maschinellen Geschirrspülmitteln und andererseits die Verwendung von Hydroxymischethern und/oder Gemischen von Hydroxymischethern und nichtionischen Tensiden als Komponente zur Verhinderang der Spannungsrißkorrosion in maschinellen Geschirrspülmitteln.As already mentioned above, hydroxy mixed ethers in particular, as a constituent from the group of surfactants, show outstanding rinse aid effects and reduce stress corrosion cracking on plastics. Furthermore, they have the advantageous property that their wetting behavior is constant over the entire usual temperature range. The use of the substances mentioned as a rinse aid component in automatic dishwashing detergents has hitherto not been described in the prior art. So far, only pure "cleaning agents" or pure "rinse aid" for automatic dishwashing have been disclosed. A combination of these two functions in one means, as provided by the present invention by incorporating a constituent from the group of the surfactants into a shaped body region which does not make up more than 40 percent of the total shaped body volume, is new. Another object of the present invention is therefore on the one hand the use of hydroxy mixed ethers and / or mixtures of hydroxy mixed ethers and nonionic surfactants as a rinse aid component in automatic dishwashing detergents and on the other hand the use of hydroxy mixed ethers and / or mixtures of hydroxy mixed ethers and nonionic surfactants as a component for preventing stress corrosion cracking in machine dishwashers Dishwashing detergents.
Hierbei kann es vorteilhaft sein, die Hydroxymischether nicht alleine, sondern in Mischung mit weiteren Tensiden, vorzugsweise nichtionischen Tensiden und insbesondere mit Nio- tensiden aus der Gruppe der ethoxylierten Fettalkohole, einzusetzen. Verwendungen, die dadurch gekennzeichnet sind, daß die Hydroxymischether im Gemisch mit Fettalkohole-
thoxylaten vorliegen, sind demnach bevorzugt. Selbstvertändlich können im Rahmen der bevorzugten erfindungsgemäßen Verwendung zusätzlich zu den ethoxylierten Fettalkoholen auch propoxylierte oder ethoxylierte und propoxylierte Fettalkohole eingesetzt werden. Solche bevorzugten Verwendungen sind dadurch gekennzeichnet, daß die Hydroxymischether im Gemisch mit Fettalkoholethoxy-propoxylaten vorliegen.It may be advantageous here to use the hydroxy mixed ethers not alone, but in a mixture with other surfactants, preferably nonionic surfactants and in particular with nonionic surfactants from the group of ethoxylated fatty alcohols. Uses which are characterized in that the hydroxy mixed ethers in a mixture with fatty alcohols Thoxylates are therefore preferred. In the context of the preferred use according to the invention, propoxylated or ethoxylated and propoxylated fatty alcohols can also be used in addition to the ethoxylated fatty alcohols. Such preferred uses are characterized in that the hydroxy mixed ethers are present in a mixture with fatty alcohol ethoxy propoxylates.
Wie vorstehend beschrieben, sind Mittel, welche gleichzeitig als maschinelle Geschirrspülmittel und als Klarspülmittel für Geschirrspülmaschinen dienen, im Stand der Technik bislang unbekannt. Auxch der Einsatz von Hydroxymischethern in Reinigungsmitteln für das maschinelle Geschirrspülen war bislang nicht bekannt. Geschirrspülmittel, die Hydroxymischether und/oder Gemische von Hydroxymischethern und nichtionischen Tensiden enthalten, sind daher ein weiterer Gegenstand der vorliegenden Erfindung.
As described above, agents which simultaneously serve as automatic dishwashing detergents and as rinse aid for dishwashers have hitherto been unknown in the prior art. Auxch was previously not aware of the use of hydroxy mixed ethers in cleaning agents for automatic dishwashing. Dishwashing detergents which contain hydroxy mixed ethers and / or mixtures of hydroxy mixed ethers and nonionic surfactants are therefore a further subject of the present invention.
BeispieleExamples
Die folgenden Rezepturen wurden gemischt und zu Formköφern veφreßt. Die in Klammern angegebenen Inhaltsstoffe sind beispielhaft für die Substanzklasse können aber durch andere in der .Anmeldung aufgezählte Substanzen ersetzt werden. Die Rahmenrezepturen stellen bevorzugte Bereiche der Erfindung dar.The following recipes were mixed and pressed into shaped bodies. The ingredients in parentheses are examples of the substance class but can be replaced by other substances listed in the application. The frame formulations represent preferred areas of the invention.
Bei der Messung der Wirksamkeit wurde der jeweils ausgewählte Inhaltsstoff (I) in den erfindungsgemäßen Bereich überführt. In dem anderen Bereich (den anderen Bereichen) wurde er erfindungsgemäß reduziert, bzw. ganz weggelasssen, bevor die Untersuchungen durchgeführt wurden. Eine mögliche Rahmenrezeptur (Ra) und Versuchsrezepturen (Va) (Angaben in Gew.-%):When measuring the effectiveness, the selected ingredient (I) was transferred to the area according to the invention. In the other area (the other areas) it was reduced according to the invention, or left out entirely before the investigations were carried out. A possible framework recipe (Ra) and test recipes (Va) (in% by weight):
Das Buildersystem der obigen Rahmenrezeptur kann auch folgendermaßen zusammengesetzt werden (alle anderen Inhaltsstoffe gleich, wie bei a).
The builder system of the framework recipe above can also be composed as follows (all other ingredients are the same as in a).
Als Rahmenrezeptur (R) für die vorliegende .Anmeldung kann auch gelten (Gew.-%): Als Versuchsrezeptur (V) wurde genutzt:The following may also apply as a basic formulation (R) for the present application (% by weight): The following was used as an experimental formulation (V):
Als Rahmenrezeptur (R) für die vorliegende Anmeldung kann auch gelten (Gew.-%): Als Versuchsrezeptur (V) wurde genutzt:
The following can also be used as the basic formulation (R) for the present application (% by weight): The following was used as the test formulation (V):
Als Rahmenrezeptur (R) für die vorliegende .Anmeldung kann auch gelten (Gew.-%): Als Versuchsrezeptur (V) wurde genutzt:The following may also apply as a basic formulation (R) for the present application (% by weight): The following was used as an experimental formulation (V):
Als Rahmenrezeptur (R) für die vorliegende .Anmeldung kann auch gelten (Gew.-%): Als Versuchsrezeptur (V) wurde genutzt:The following may also apply as a basic formulation (R) for the present application (% by weight): The following was used as an experimental formulation (V):
Als Rahmenrezeptur (R) für die vorliegende .Anmeldung kann gelten (Angaben in Gew.- %):
Als Versuchsrezeptur (V) wurde genutzt:The following general formula (R) for this application can apply (data in% by weight): The following test formulation (V) was used:
Als Rahmenrezeptur (R) für die vorliegende .Anmeldung kann gelten (.Angaben in Gew.The following general formula (R) for this.
%):%):
Als Nersuchsrezeptur (V) wurde genutzt:The following was used as the test formulation (V):
Eine weitere Rahmenrezeptur (R) (Gew.-%) und Versuchsrezepturen (V) wurden geprüft:A further basic formulation (R) (% by weight) and experimental formulations (V) were tested:
Sollten in einem erfindungsgemäßen Formköφer mehrere Phasen enthalten sein, so kann jede Rezeptur auch die Bestandteile einer einzelnen Phase sein, d.h. die Anteile beziehen sich dann nicht wie üblich auf die Gesamtrezeptur, sondern auf die Zusammensetzung der einzelnen Phase.
In jedem der Rezepturen können natürlich auch noch andere in MGSM übliche Inhaltsstoffe (z. B. Füllstoffe, Konservierungsmittel, u.a.) in äußerst geringen Mengen enthalten sein, wobei die anderen Bestandteile anteilig entsprechend zu variieren sind.If several phases are contained in a molded article according to the invention, each formulation can also be the constituents of an individual phase, ie the proportions then do not relate to the overall formulation as usual, but to the composition of the individual phase. Of course, each of the recipes can also contain other ingredients commonly used in MGSM (e.g. fillers, preservatives, etc.) in extremely small quantities, with the other ingredients being proportionately varied accordingly.
Die Herstellung der erfindungsgemäßen Formköφer benutzt Schritte, die dem Wissen des Fachmanns auf diesem Gebiet in anderem Zusammenhang bekannt sind. Eine bevorzugte Ausgestaltungform des Formköφers des ersten Anspraches enthält eine Mulde in einer Tablette, wobei diese Mulde den Inhaltsstoff (I) beinhaltet. Die Herstellung geschieht in einem bevorzugten Fall so, daß man einen Vertiefung in einen Formköφer prägt und diese Vertiefung befüllt. Die Prägung kann auf einer Rundläufeφresse der Fa. Korsch erfolgen. Im vorliegenden Fall wurde eine Tablettenpresse der Fa. Fette eingesetzt. Eine runde Tablettenform (26 X 36 mm) wurde gewählt und mit einem Stempel 5 mm tief auf einer Seite geprägt, wobei die Grundfläche so gewählt war, daß ein Volumen von 1 ml eingefüllt werden konnte und die Tablette hinterher wieder eine glatte Oberfläche besaß.The production of the molded body according to the invention uses steps which are known in a different context to the knowledge of the person skilled in the art in this field. A preferred embodiment of the molded body of the first speech contains a depression in a tablet, this depression containing the ingredient (I). In a preferred case, the production takes place in such a way that a depression is embossed into a molded body and this depression is filled. The embossing can be done on a Korsch rotary press. In the present case, a tablet press from Fette was used. A round tablet shape (26 X 36 mm) was selected and embossed on one side with a stamp 5 mm deep, the base area being chosen such that a volume of 1 ml could be filled in and the tablet subsequently had a smooth surface.
Danach wurde ein flüssiges Gemisch aus Paraffin und einem Wirkstoff (I) (im vorliegenden Fall Tensid (Dehypon LS54, Hydroxymischether, Gemische der beiden Substanzklassen) eingefüllt und erkalten gelassen. Diese Abkühlung kann durch gängige apparative Methoden unterstützt werden.A liquid mixture of paraffin and an active ingredient (I) (in the present case surfactant (Dehypon LS54, hydroxy mixed ether, mixtures of the two classes of substances) was then poured in and allowed to cool. This cooling can be supported by conventional apparatus methods.
Wie bereits erwähnt wurde der Inhaltsstoff (I) erfindungsgemäß in der entsprechenden Rezeptur, die den eingefüllten Bereich umgibt, zuvor in der Menge reduziert und in den vorliegenden Beispielen und Untersuchungen in den umgebenden Bereichen weggelassen.As already mentioned, the ingredient (I) according to the invention was previously reduced in quantity in the corresponding recipe which surrounds the filled area and was omitted in the surrounding areas in the examples and investigations at hand.
In Vergleichsversuchen mit homogenen (nichterfindungsgemäßer Inhaltsstoff (I)) und einigen handelsüblichen Tabletten erwiesen sich die erfindungsgemäßen Tabletten als überlegen.In comparison tests with homogeneous (noninventive ingredient (I)) and some commercially available tablets, the tablets according to the invention proved to be superior.
Zusätzlich wurden die besonderen Eigenschaften der erfindungsgemäßen Mittel durch technisch ungeschulte Personen unter praxisrelevanten Bedingungen im Vergleich zu homogenen Tabletten übeφriift. Dabei wurde außer Hinweisen für die Dosierung und allgemeinen Sicherheitshinweisen kein Einfluß auf die Handhabe der Mittel durch den Personenkreis in handelsüblichen Geschirrspülmaschinen genommen. Dieser Vergleichsversuch fiel besonders gut aus. Hier wurden die Reinigungsergebnisse als besonders günstig bewertet.
In einem Versuch wurden Proben analog Ra, bzw. Val, die Tenside als Wirkstoff (I) enthielten einmal in homogener Verteilung in der Tablette und einmal gemäß Ansprach 1 eingesetzt, so daß die Tensidkomponente weitgehend von anderen Komponenten getrennt war. Die Reingungsergebnisse waren sehr gut.In addition, the special properties of the agents according to the invention were checked by technically untrained persons under practical conditions in comparison to homogeneous tablets. Apart from instructions for the dosage and general safety instructions, no influence was taken on the handling of the agents by the group of people in standard dishwashers. This comparison test turned out to be particularly good. The cleaning results were rated as particularly favorable here. In an experiment, samples analogous to Ra or Val were used which contained surfactants as active ingredient (I) once in a homogeneous distribution in the tablet and once according to approach 1, so that the surfactant component was largely separated from other components. The cleaning results were very good.
Es wurden auch die Klarspülergebnisse geprüft. Bei der Effekt bei der Nutzung eines Gemisches aus Tensid (Hydroxymischether) und Paraffin in einem Standardprogramm bei 55 °C waren die Ergebnisse besser als bei Formköφern ohne Bereich (I), homogen verteilter Komponente (I) und handelsüblichen Reinigern. Die Ergebnisse zeigen einen positiven Einfluß des Paraffin. Auch die Änderung des Schmelzbereichs des Paraffins hat einen Effekt auf das Spülergebnis.The rinse aid results were also checked. With the effect of using a mixture of surfactant (hydroxy mixed ether) and paraffin in a standard program at 55 ° C, the results were better than with molded articles without area (I), homogeneously distributed component (I) and commercially available cleaners. The results show a positive influence of the paraffin. Changing the melting range of the paraffin also has an effect on the washing result.
Die Ergebnisse zeigen eindeutig, daß die erfmdungsgemäßen Mittel üblichen Geschirrspülmitteltabletten überlegen sind.The results clearly show that the agents according to the invention are superior to conventional dishwasher tablets.
In weiteren Beispielen wurden Schmelzemulsionen von unterschiedlichen Tensiden in Hüllsubstanzen hergestellt, die die positiven Effekte belegen. Hierbei wurden durch Ver- pressen mit einem Preßstempel, der einen Zapfen aufwies, Muldenformköφer (Gewicht: 24 g) hergestellt. Die Zusammensetzung (in Gew.-%, bezogen auf das Vorgemisch) und damit der Muldenformköφer zeigt die nachstehende Tabelle 1 :In further examples, melt emulsions of different surfactants were produced in coating substances, which prove the positive effects. Here, trough-shaped bodies (weight: 24 g) were produced by pressing with a press ram which had a pin. Table 1 below shows the composition (in% by weight, based on the premix) and thus the mold body:
Tabelle 1: Zusammensetzung des Vorgemischs (Gew.-%):Table 1: Composition of the premix (% by weight):
Durch Erhitzen des jeweiligen Hüllmaterials und Einrühren der Aktivsubstanz (Tenside) wurden Schmelzdispersionen SDE 1 bis 5 hergestellt, deren Zusammensetzung (Gew.-%, bezogen auf die Schmelze) in der nachstehenden Tabelle angegeben ist: By heating the respective shell material and stirring in the active substance (surfactants), melt dispersions SDE 1 to 5 were produced, the composition (% by weight, based on the melt) of which is given in the table below:
Poly-(12-hydroxystearinsäure)polyglycerinester, Dehymuls" KE 3360 (Grünau)Poly (12-hydroxystearic acid) polyglycerol ester, Dehymuls "KE 3360 (Grünau)
** Cι2-ι4-Fettalkohol mit 5 EO und 4 EO (Henkel) *** Fettalkoholpolyglycolether, modifiziertt (Henkel) **** Fettalkoholalkoxylat (Olin Chemicals)** Cι 2 -ι 4 fatty alcohol with 5 EO and 4 EO (Henkel) *** fatty alcohol polyglycol ether, modified (Henkel) **** fatty alcohol alkoxylate (Olin Chemicals)
Die Schmelzemulsionen wurden in der vorstehend genannten Weise in die Formköφer eingefüllt und erkalten gelassen. Hierbei wiesen die Formköφer vor dem Befallen ein Gewicht von 24 g auf und wurden mit jeweils 1,3 g der Schmelzemulsion befüllt. Die Reini- gungsleistung (Klaφspüleffekt) der mit den Schmelzemulsionen SDE 1 bis SDE 5 befüllten Formköφer El bis E5 wurde an unterschiedlichen Substraten (Teller, Gläser, Messer, Kunststoffteller) getestet. Hierzu wurden die verschmutzten Gegenstände in einer haushaltsüblichen Geschirrspülmaschine, deren Klarspültank geleert war, gereinigt:The melt emulsions were poured into the moldings in the manner mentioned above and allowed to cool. The moldings had a weight of 24 g before being infested and were each filled with 1.3 g of the melt emulsion. The cleaning performance (rinsing effect) of the molded bodies El to E5 filled with the melt emulsions SDE 1 to SDE 5 was tested on different substrates (plates, glasses, knives, plastic plates). For this purpose, the soiled objects were cleaned in a normal household dishwasher, whose rinse aid tank was empty:
Der Klarspüleffekt der Mittel wurde visuell von Fachleuten durchgeführt und benotet, wobei auf einer Skala von 0-8 die Note "0" Wasserflecken und kein Unterschied zum Spülen ohne Klarspüler bedeutet und "8" absolut sauber bedeutet.The rinse aid effect of the detergents was carried out visually by experts and was graded, the score "0" meaning water stains and no difference to rinsing without rinse aid on a scale of 0-8 and "8" meaning absolutely clean.
Die Klarspüleffekte wurden für Waschbedingungen 55 °C / 16 °d Wasserhärte im Hauptspülgang gemessen (d. h. "harte Bedingungen"). Als Spülmaschine wurde eine Miele G 590 mit Universalprogramm benutzt. Die nachstehende Tabelle zeigt die erzielten Klarspülergebnisse der Mittel El bis E5 im Vergleich zu einem unbefüllten Formköφer V
The rinse aid effects were measured for washing conditions 55 ° C / 16 ° d water hardness in the main rinse cycle (ie "hard conditions"). A Miele G 590 with a universal program was used as the dishwasher. The table below shows the rinse aid results achieved with agents El to E5 compared to an unfilled molded article V
Die Ergebnisse zeigen, daß die erfindungsgemäßen Formköφer El bis E5 dem Vergleichs- formköφer V bei der Erzielung von Klarspüleffekten weit überlegen sind.
The results show that the shaped bodies E1 to E5 according to the invention are far superior to the comparative shaped body V in achieving rinse aid effects.
Claims
1. Formköφer enthaltend Builderstoffe, Alkaliträger, Bleichmittel und Enzyme, dadurch gekennzeichnet, daß in einem Bereich nicht größer als 40 Vol.-%, mehr als 80 Gew.-%, einer Aktivsubstanz (I) mit einem Bestandteil aus der Gruppe der Tenside enthalten ist.1. Shaped body containing builders, alkali carriers, bleaches and enzymes, characterized in that in an area not greater than 40 vol .-%, more than 80 wt .-%, contain an active substance (I) with a component from the group of surfactants is.
2. Formköφer nach Anspruch 1, dadurch gekennzeichnet, daß der Bereich zwischen 1 und 30 Vol.-%, besonders bevorzugt zwischen 2 und 25 Vol.-%, ganz besonders bevorzugt zwischen 3 und 20 Vol.-% des Formköφers mehr als 90 Gew.-%, besonders bevorzugt mehr als 95 Gew.-%, ganz besonders bevorzugt die Gesamtmenge eines vorhandenen Inhaltsstoffes (I) enthalten ist.2. molded body according to claim 1, characterized in that the range between 1 and 30 vol .-%, particularly preferably between 2 and 25 vol .-%, very particularly preferably between 3 and 20 vol .-% of the molded body more than 90 wt %, particularly preferably more than 95% by weight, very particularly preferably the total amount of an ingredient (I) present.
3. Foimköφer nach Ansprach 1, dadurch gekennzeichnet, daß dieser Inhaltsstoff (I) ein Gemisch aus Tensid und einem weiteren Stoff aus der Gruppe gebildet aus Bleichaktivator und/oder Bleichmittel aus der Gruppe der Chlor- und/oder Sauerstoffbleichmittel und/oder Silberschutzmittel und/oder Enzym und/oder Soil-Release-Verbindung und/oder einer Komponente zur Löslichkeitskontrolle und/oder weiteren Inhaltsstoffen ist.3. Foimköφer according spoke 1, characterized in that this ingredient (I) is a mixture of surfactant and another substance from the group consisting of bleach activator and / or bleach from the group of chlorine and / or oxygen bleach and / or silver protection and / or enzyme and / or soil release compound and / or a component for solubility control and / or further ingredients.
4. Formköφer nach einem der vorstehenden .Ansprüche, dadurch gekennzeichnet, daß mindestens ein Sauerstoffbleiclimittel ausgewählt aus der Gruppe der Alkaliperborate, Alkalipercarbonate, der organischen Persäuren und Wasserstoffperoxid enthalten ist.4. Molded body according to one of the preceding claims, characterized in that at least one oxygen lead agent selected from the group of alkali perborates, alkali percarbonates, organic peracids and hydrogen peroxide is contained.
5. Formköφer nach einem der vorstehenden .Ansprüche, dadurch gekennzeichnet, daß der Inhaltsstoff (I) mindestens ein Tensid und mindestens eine schmelzbare Komponente zur Löslichkeitskontrolle ausgewählt aus der Gruppe der Tenside, der Paraffine, der Miakrowachse und/oder der höhermolekularen Polyethylenglycole und/oder Sprengmittel enthält.5. Molded body according to one of the preceding claims, characterized in that the ingredient (I) has at least one surfactant and at least one fusible component for solubility control selected from the group of the surfactants, the paraffins, the miacrow waxes and / or the higher molecular weight polyethylene glycols and / or Contains explosives.
6. Formköφer nach einem der vorstehenden .Ansprüche, dadurch gekennzeichnet, daß ein Bleichaktivator, bevorzugt aus der Gruppe der mehrfach acylierte Alkylendiamine, insbesondere Tetraacetylethylendiamin (TAED), N-Acylimide, insbesondere N- Nonanoylsuccinimid (NOSI), acylierte Phenolsulfonate, insbesondere n-Nonanoyl- oder Isononanoyloxybenzolsulfonat (n- bzw. iso-NOBS), MMA und/oder der Gruppe der Mangan und/oder Cobaltsalze und/oder -komplexe, besonders bevorzugt der Cobalt(ammin)-Komplexe, der Cobalt(acetat)-Komplexe, der Cobalt(Carbonyl)-
Komplexe, der Chloride des Cobalts oder Mangans, des Mangansulfats, vorzugsweise in Mengen von 1 Gew.-% bis 10 Gew.-%, insbesondere 2 Gew.-% bis 8 Gew.-%, bezogen auf gesamtes Mittel, enthalten ist6. Shaped body according to one of the preceding claims, characterized in that a bleach activator, preferably from the group of polyacylated alkylenediamines, especially tetraacetylethylenediamine (TAED), N-acylimides, especially N-nonanoylsuccinimide (NOSI), acylated phenolsulfonates, especially n- Nonanoyl or isononanoyloxybenzenesulfonate (n- or iso-NOBS), MMA and / or the group of manganese and / or cobalt salts and / or complexes, particularly preferably the cobalt (ammin) complexes, the cobalt (acetate) complexes, the cobalt (carbonyl) - Complexes, the chlorides of cobalt or manganese, of manganese sulfate, preferably in amounts of 1% by weight to 10% by weight, in particular 2% by weight to 8% by weight, based on the total agent
7. Formköφer nach einem der vorstehenden .Anspräche, dadurch gekennzeichnet, daß weiterhin ein oder mehrere Builder aus der Gruppe der Gluconate, der niedermolekularen Polycarbonsäuren und ihre Salze, der homopolymeren und copolymeren Polycarbonsäuren und ihre Salze, der Carbonate, Phosphate und Silikate, bevorzugt Trinatriumcitrat und/oder Pentanatriumtripolyphosphat und/oder Natriumcarbonat und/oder Natriumbicarbonat und/oder Gluconate und/oder silikatische Builder aus der Klasse der Disilikate und/oder Metasilikate eingesetzt wird.7. Shaped body according to one of the preceding claims, characterized in that one or more builders from the group of gluconates, low molecular weight polycarboxylic acids and their salts, homopolymeric and copolymeric polycarboxylic acids and their salts, carbonates, phosphates and silicates, preferably trisodium citrate and / or pentasodium tripolyphosphate and / or sodium carbonate and / or sodium bicarbonate and / or gluconates and / or silicate builders from the class of disilicates and / or metasilicates is used.
8. Formköφer nach einem der vorstehenden .Anspräche, dadurch gekennzeichnet, daß als Buildersystem eine Mischung aus Tripolyphosphat und/oder Natriumcarbonat und/oder Natriumdisilikat beinhaltet.8. Molded body according to one of the preceding claims, characterized in that a mixture of tripolyphosphate and / or sodium carbonate and / or sodium disilicate is included as the builder system.
9. Formköφer nach einem der vorstehenden Anspräche, dadurch gekennzeichnet, daß die Tenside ausgewählt sind aus der Gruppe der nichtionischen Tenside, bevorzugt der schwachschäumenden nichtionischen Tenside, ganz besonders bevorzugt der alkoxylierten und/oder propoxylierten Fettalkohole, der Alkylpolyglycoside, der Alkylpoly- glucamide und/oder Gemische der vorstehenden Tenside, äußerst bevorzugt aus der Gruppe der Hydroxymischether und der Gemische von Hydroxymischethern und anderen nichtionischen Tensiden9. Molded body according to one of the preceding claims, characterized in that the surfactants are selected from the group of nonionic surfactants, preferably the low-foaming nonionic surfactants, very particularly preferably the alkoxylated and / or propoxylated fatty alcohols, the alkyl polyglycosides, the alkyl polyglucamides and / or mixtures of the above surfactants, most preferably from the group of the hydroxy mixed ethers and the mixtures of hydroxy mixed ethers and other nonionic surfactants
10. Formköφer nach einem der vorstehenden .Ansprüche, dadurch gekennzeichnet, daß zusätzlich mindestens ein Silberschutzmittel aus gewählt aus der Gruppe der Triazole, der Benzotriazole, der Bisbenzotriazole, der .Aminotriazole, der Alkylaminotriazole und der Übergangsmetallsalze oder -komplexe, besonders bevorzugt Benzotriazol und/oder Alkylaminotriazol enthalten ist.10. Molded body according to one of the preceding claims, characterized in that in addition at least one silver protective agent selected from the group consisting of the triazoles, the benzotriazoles, the bisbenzotriazoles, the .amino triazoles, the alkylaminotriazoles and the transition metal salts or complexes, particularly preferably benzotriazole and / or alkylaminotriazole is included.
11. Formköφer nach .Anspruch 11, dadurch gekennzeichnet, daß die Übergangsmetallsalze ausgewählt sind aus der Gruppe der Mangan und/oder Cobaltsalze und/oder - komplexe, besonders bevorzugt der Cobalt(amin)-Komplexe, der Cobalt(acetat)- Komplexe, der Cobalt(Carbonyl)-Komplexe, der Chloride des Cobalts oder Mangans und des Mangansulfats.
11. Molded body according to claim 11, characterized in that the transition metal salts are selected from the group consisting of manganese and / or cobalt salts and / or complexes, particularly preferably the cobalt (amine) complexes, the cobalt (acetate) complexes Cobalt (carbonyl) complexes, the chlorides of cobalt or manganese and manganese sulfate.
12. Formköφer nach einem der vorgehenden .Ansprüche, dadurch gekennzeichnet, daß die Komponente und/oder die Komponenten zur Löslichkeitskontrolle ausgewählt aus der Gruppe der Paraffine, der Mil rowachse und der hochmolekularen Polyethylenglykole enthalten sind.12. Molded body according to one of the preceding claims, characterized in that the component and / or the components for solubility control selected from the group of paraffins, the Mil rowachse and the high molecular weight polyethylene glycols are included.
13. Formköφer nach einem der .Ansprüche 1 bis 13, dadurch gekennzeichnet, daß die Komponente und/oder die Komponenten zur Löslichkeitskontrolle ausgewählt aus der Gruppe der organischen Säuren, wie z. B. Citronensäure, bzw. eines Gemisches Citro- nensäure/Bicarbonat und/oder der Cellulosen und Cellulosederivate enthalten sind.13. Molded body according to one of claims 1 to 13, characterized in that the component and / or the components for solubility control selected from the group of organic acids, such as. B. citric acid, or a mixture of citric acid / bicarbonate and / or the celluloses and cellulose derivatives are contained.
14. Formköφer nach einem der vorstehenden .Ansprüche, dadurch gekennzeichnet, daß eine der oder die Bleichkomponente, besonders die Chlorkomponente nicht in einer Phase mit der Parfümkomponente zusammen konfektioniert wird.14. Molded body according to one of the preceding claims, characterized in that one or more of the bleaching components, especially the chlorine component, are not assembled together with the perfume component in one phase.
15. Formköφer nach einem der vorstehenden .Ansprüche, dadurch gekennzeichnet, daß die Silberschutzkomponente nicht mit einer der oder der Bleichkomponente konfektioniert wird.15. Molded body according to one of the preceding claims, characterized in that the silver protection component is not made up with one of the bleaching components.
16. Formköφer nach einem der vorstehenden Anspräche, dadurch gekennzeichnet, daß eine der oder die Komponente zur Löslichkeitskontrolle zusammen mit dem Bleichaktivator konfektioniert wird.16. molded article according to one of the preceding claims, characterized in that one of the component or components for solubility control is assembled together with the bleach activator.
17. Formköφer nach einem der vorstehenden .Ansprüche, dadurch gekennzeichnet, daß eine der oder die Komponente zur Löslichkeitskontrolle zusammen mit den Enzymen konfektioniert wird.17. Molded body according to one of the preceding claims, characterized in that one of the component or components for solubility control is assembled together with the enzymes.
18. Formköφer nach einem der vorstehenden .Ansprüche, dadurch gekennzeichnet, daß eine der oder die Komponente zur Löslichkeitskontrolle zusammen mit dem Bleichmittel konfektioniert wird.18. Shaped body according to one of the preceding claims, characterized in that one of the component or components for solubility control is made up together with the bleaching agent.
19. Formköφer nach einem der vorstehenden Anspräche, dadurch gekennzeichnet, daß eine der oder die Komponente zur Löslichkeitskontrolle zusammen mit der Silberschutzkomponente konfektioniert wird.19. Molded body according to one of the preceding claims, characterized in that one of the component or components for solubility control is assembled together with the silver protection component.
20. Verwendung von Hydroxymischethern und/oder Gemischen von Hydroxymischethern und nichtionischen Tensiden als Klarspülkomponente in maschinellen Geschirrspül- mitteln.
20. Use of hydroxy mixed ethers and / or mixtures of hydroxy mixed ethers and nonionic surfactants as rinse aid components in automatic dishwashing detergents.
21. Veiwendung von Hydroxymischethern und/oder Gemischen von Hydroxymischethern und nichtionischen Tensiden als Komponente zur Verhinderang der Spannungsrißkorrosion in maschinellen Geschirrspülmitteln.21. Use of hydroxy mixed ethers and / or mixtures of hydroxy mixed ethers and nonionic surfactants as a component for preventing stress corrosion cracking in automatic dishwashing detergents.
22. Verwendung nach .Anspruch 29 oder 30, dadurch gekennzeichnet, daß die Hydroxymischether im Gemisch mit Fettalkoholethoxylaten vorliegen.22. Use according to .Anspruch 29 or 30, characterized in that the hydroxy mixed ethers are present in a mixture with fatty alcohol ethoxylates.
23. Verwendung nach Ansprach 29 bis 31, dadurch gekennzeichnet, daß die Hydroxymischether im Gemisch mit Fettalkoholethoxy-propoxylaten vorliegen.23. Use according to spoke 29 to 31, characterized in that the hydroxy mixed ethers are present in a mixture with fatty alcohol ethoxy propoxylates.
24. Geschirrspülmittel enthaltend Hydroxymischether und/oder Gemische von Hydroxymischethern und nichtionischen Tensiden.
24. Dishwashing detergent containing hydroxy mixed ethers and / or mixtures of hydroxy mixed ethers and nonionic surfactants.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19758176 | 1997-12-30 | ||
DE19758176A DE19758176A1 (en) | 1997-12-30 | 1997-12-30 | Dishwasher detergent tablets with surfactants |
PCT/EP1998/008373 WO1999035225A2 (en) | 1997-12-30 | 1998-12-21 | Moulded body dishwasher detergents containing surfactants |
CA002300643A CA2300643A1 (en) | 1997-12-30 | 2000-03-07 | Dishwasher detergent shaped bodies containing surfactants |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1045893A2 true EP1045893A2 (en) | 2000-10-25 |
Family
ID=25681619
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP98966386A Ceased EP1045893A2 (en) | 1997-12-30 | 1998-12-21 | Moulded body dishwasher detergents containing surfactants |
Country Status (9)
Country | Link |
---|---|
EP (1) | EP1045893A2 (en) |
JP (1) | JP2002500264A (en) |
CA (1) | CA2300643A1 (en) |
CZ (1) | CZ20002487A3 (en) |
DE (1) | DE19758176A1 (en) |
HU (1) | HUP0100620A2 (en) |
PL (1) | PL342079A1 (en) |
SK (1) | SK9992000A3 (en) |
WO (1) | WO1999035225A2 (en) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE29911484U1 (en) * | 1998-07-17 | 2000-02-24 | The Procter & Gamble Co., Cincinnati, Ohio | Detergent tablet |
DE29911486U1 (en) * | 1998-07-17 | 1999-11-18 | The Procter & Gamble Co., Cincinnati, Ohio | Detergent tablet |
GB9911949D0 (en) | 1999-05-21 | 1999-07-21 | Unilever Plc | Detergent compositions |
DE29911487U1 (en) * | 1999-07-01 | 1999-11-25 | The Procter & Gamble Co., Cincinnati, Ohio | Detergent tablet |
DE29911485U1 (en) * | 1999-07-01 | 1999-11-25 | The Procter & Gamble Co., Cincinnati, Ohio | Detergent tablet |
DE19937428A1 (en) * | 1999-08-07 | 2001-02-08 | Henkel Kgaa | Detergent tablets |
DE19962883A1 (en) * | 1999-12-24 | 2001-07-12 | Cognis Deutschland Gmbh | Detergent tablets |
GB2375543A (en) * | 2001-05-18 | 2002-11-20 | Reckitt Benckiser Inc | Laundry additive compositions |
GB2377451A (en) † | 2001-07-11 | 2003-01-15 | Reckitt Benckiser Nv | Delayed release cleaning composition for automatic dishwashers |
DE10137925A1 (en) * | 2001-08-07 | 2003-02-20 | Cognis Deutschland Gmbh | Mixtures for improving hard surface wettability especially in machine dish washing comprise Gemini surfactant and polyethylene glycol |
DE10209156A1 (en) * | 2002-03-01 | 2003-09-18 | Henkel Kgaa | Shaped body with subsequent surfactant dosage |
DE102004039921A1 (en) * | 2004-08-18 | 2006-03-02 | Henkel Kgaa | Rinse aid containing washing and cleaning agents with sulfur-containing amino acids |
DE102007019457A1 (en) * | 2007-04-25 | 2008-10-30 | Basf Se | Machine dishwashing detergent with excellent rinse performance |
JP2012111810A (en) * | 2010-11-22 | 2012-06-14 | Kao Corp | Powder detergent composition for use in automatic washer |
JP6067168B1 (en) * | 2016-05-30 | 2017-01-25 | 株式会社ニイタカ | Cleaning composition for automatic cleaning machine |
US10889783B2 (en) | 2017-11-14 | 2021-01-12 | Ecolab Usa Inc. | Solid controlled release caustic detergent compositions |
CN114222808A (en) | 2019-09-27 | 2022-03-22 | 埃科莱布美国股份有限公司 | Concentrated two-in-one dishwasher detergent and rinse aid |
WO2024188924A1 (en) * | 2023-03-16 | 2024-09-19 | Evonik Operations Gmbh | Biosurfactants on area-measured plastic articles |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4569781A (en) * | 1978-02-07 | 1986-02-11 | Economics Laboratory, Inc. | Cast detergent-containing article and method of using |
DE3541147A1 (en) * | 1985-11-21 | 1987-05-27 | Henkel Kgaa | CLEANER COMPACT |
GB9015504D0 (en) * | 1990-07-13 | 1990-08-29 | Unilever Plc | Detergents composition |
US5133892A (en) * | 1990-10-17 | 1992-07-28 | Lever Brothers Company, Division Of Conopco, Inc. | Machine dishwashing detergent tablets |
GB9022724D0 (en) * | 1990-10-19 | 1990-12-05 | Unilever Plc | Detergent compositions |
AU661491B2 (en) * | 1991-05-14 | 1995-07-27 | Ecolab Inc. | Two part chemical concentrate |
US5294365A (en) * | 1991-12-12 | 1994-03-15 | Basf Corporation | Hydroxypolyethers as low-foam surfactants |
US5576281A (en) * | 1993-04-05 | 1996-11-19 | Olin Corporation | Biogradable low foaming surfactants as a rinse aid for autodish applications |
GB2327949A (en) * | 1997-08-02 | 1999-02-10 | Procter & Gamble | Detergent tablet |
DE19738866A1 (en) * | 1997-09-05 | 1999-03-11 | Henkel Kgaa | Low-foaming surfactant mixtures with hydroxy mixed ethers |
-
1997
- 1997-12-30 DE DE19758176A patent/DE19758176A1/en not_active Withdrawn
-
1998
- 1998-12-21 WO PCT/EP1998/008373 patent/WO1999035225A2/en not_active Application Discontinuation
- 1998-12-21 EP EP98966386A patent/EP1045893A2/en not_active Ceased
- 1998-12-21 SK SK999-2000A patent/SK9992000A3/en unknown
- 1998-12-21 CZ CZ20002487A patent/CZ20002487A3/en unknown
- 1998-12-21 HU HU0100620A patent/HUP0100620A2/en unknown
- 1998-12-21 JP JP2000527612A patent/JP2002500264A/en active Pending
- 1998-12-21 PL PL98342079A patent/PL342079A1/en unknown
-
2000
- 2000-03-07 CA CA002300643A patent/CA2300643A1/en not_active Abandoned
Non-Patent Citations (1)
Title |
---|
See references of WO9935225A3 * |
Also Published As
Publication number | Publication date |
---|---|
JP2002500264A (en) | 2002-01-08 |
SK9992000A3 (en) | 2000-12-11 |
CA2300643A1 (en) | 2000-05-29 |
HUP0100620A2 (en) | 2001-06-28 |
CZ20002487A3 (en) | 2001-11-14 |
DE19758176A1 (en) | 1999-07-01 |
PL342079A1 (en) | 2001-05-21 |
WO1999035225A2 (en) | 1999-07-15 |
WO1999035225A3 (en) | 1999-09-23 |
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