EP0808891A1 - Saure Reinigungszusammensetzungen - Google Patents
Saure Reinigungszusammensetzungen Download PDFInfo
- Publication number
- EP0808891A1 EP0808891A1 EP96201366A EP96201366A EP0808891A1 EP 0808891 A1 EP0808891 A1 EP 0808891A1 EP 96201366 A EP96201366 A EP 96201366A EP 96201366 A EP96201366 A EP 96201366A EP 0808891 A1 EP0808891 A1 EP 0808891A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- acid
- carbon atoms
- composition
- linear
- branched alkyl
- 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.)
- Withdrawn
Links
- 239000000203 mixture Substances 0.000 title claims description 140
- 230000002378 acidificating effect Effects 0.000 title claims description 36
- 238000004140 cleaning Methods 0.000 title claims description 20
- 150000001412 amines Chemical class 0.000 claims description 62
- 125000004432 carbon atom Chemical group C* 0.000 claims description 47
- 239000002253 acid Substances 0.000 claims description 41
- 125000000217 alkyl group Chemical group 0.000 claims description 41
- 239000004094 surface-active agent Substances 0.000 claims description 36
- 239000007788 liquid Substances 0.000 claims description 29
- 229920006395 saturated elastomer Polymers 0.000 claims description 22
- 239000000344 soap Substances 0.000 claims description 18
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 15
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 15
- 239000011976 maleic acid Substances 0.000 claims description 15
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 15
- 239000003093 cationic surfactant Substances 0.000 claims description 10
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 9
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- 150000007522 mineralic acids Chemical class 0.000 claims description 7
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical compound NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 claims description 7
- 150000007524 organic acids Chemical class 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 4
- VICYBMUVWHJEFT-UHFFFAOYSA-N dodecyltrimethylammonium ion Chemical class CCCCCCCCCCCC[N+](C)(C)C VICYBMUVWHJEFT-UHFFFAOYSA-N 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 239000001117 sulphuric acid Substances 0.000 claims description 4
- 235000011149 sulphuric acid Nutrition 0.000 claims description 4
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- 229910017604 nitric acid Inorganic materials 0.000 claims description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 18
- 150000007513 acids Chemical class 0.000 description 18
- 239000002736 nonionic surfactant Substances 0.000 description 13
- 239000004615 ingredient Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000002888 zwitterionic surfactant Substances 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 235000013162 Cocos nucifera Nutrition 0.000 description 4
- 244000060011 Cocos nucifera Species 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- 125000000129 anionic group Chemical group 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 125000002091 cationic group Chemical group 0.000 description 4
- -1 e.g. Substances 0.000 description 4
- 150000003141 primary amines Chemical class 0.000 description 4
- 150000003335 secondary amines Chemical class 0.000 description 4
- 150000003512 tertiary amines Chemical class 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 239000003945 anionic surfactant Substances 0.000 description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- XJWSAJYUBXQQDR-UHFFFAOYSA-M dodecyltrimethylammonium bromide Chemical compound [Br-].CCCCCCCCCCCC[N+](C)(C)C XJWSAJYUBXQQDR-UHFFFAOYSA-M 0.000 description 3
- 125000001165 hydrophobic group Chemical group 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 2
- PSBDWGZCVUAZQS-UHFFFAOYSA-N (dimethylsulfonio)acetate Chemical compound C[S+](C)CC([O-])=O PSBDWGZCVUAZQS-UHFFFAOYSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- CXRFDZFCGOPDTD-UHFFFAOYSA-M Cetrimide Chemical compound [Br-].CCCCCCCCCCCCCC[N+](C)(C)C CXRFDZFCGOPDTD-UHFFFAOYSA-M 0.000 description 2
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical compound C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 description 2
- 150000008043 acidic salts Chemical class 0.000 description 2
- 239000002280 amphoteric surfactant Substances 0.000 description 2
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000007046 ethoxylation reaction Methods 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000004519 grease Substances 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 2
- 239000001095 magnesium carbonate Substances 0.000 description 2
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- ONLRKTIYOMZEJM-UHFFFAOYSA-N n-methylmethanamine oxide Chemical compound C[NH+](C)[O-] ONLRKTIYOMZEJM-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000001453 quaternary ammonium group Chemical group 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 125000000547 substituted alkyl group Chemical group 0.000 description 2
- 229940117986 sulfobetaine Drugs 0.000 description 2
- 125000001273 sulfonato group Chemical class [O-]S(*)(=O)=O 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical class OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
- JBVOQKNLGSOPNZ-UHFFFAOYSA-N 2-propan-2-ylbenzenesulfonic acid Chemical compound CC(C)C1=CC=CC=C1S(O)(=O)=O JBVOQKNLGSOPNZ-UHFFFAOYSA-N 0.000 description 1
- CVLHGLWXLDOELD-UHFFFAOYSA-N 4-(Propan-2-yl)benzenesulfonic acid Chemical compound CC(C)C1=CC=C(S(O)(=O)=O)C=C1 CVLHGLWXLDOELD-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 229910006069 SO3H Inorganic materials 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 239000002535 acidifier Substances 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 125000005647 linker group Chemical group 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium group Chemical group [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- SZEMGTQCPRNXEG-UHFFFAOYSA-M trimethyl(octadecyl)azanium;bromide Chemical compound [Br-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C SZEMGTQCPRNXEG-UHFFFAOYSA-M 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000003643 water by type Substances 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/042—Acids
-
- 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
- C11D1/75—Amino oxides
-
- 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
- C11D1/835—Mixtures of non-ionic with cationic 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
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2075—Carboxylic acids-salts thereof
-
- 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
- C11D3/20—Organic compounds containing oxygen
- C11D3/2075—Carboxylic acids-salts thereof
- C11D3/2082—Polycarboxylic acids-salts thereof
-
- 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
- C11D3/20—Organic compounds containing oxygen
- C11D3/2075—Carboxylic acids-salts thereof
- C11D3/2086—Hydroxy carboxylic acids-salts thereof
-
- 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
- C11D3/30—Amines; Substituted amines ; Quaternized amines
-
- 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
- C11D1/38—Cationic compounds
- C11D1/40—Monoamines or polyamines; Salts thereof
Definitions
- the present invention relates to cleaning compositions for hard-surfaces. More specifically, the compositions of the present invention give optimal performance in removing limescale-containing stains typically found in a kitchen or in a bathroom.
- Tap water contains a certain amount of solubilized ions which upon water evaporation eventually deposit as salts such as calcium carbonate on surfaces which are often in contact with said water, resulting in an unaesthetic aspect of said surfaces. This limescale formation and deposition phenomenon is even more acute in places where water is particularly hard.
- liquid acidic limescale removal compositions do not perform equally well on all limescale-containing stains, particularly on limescale-containing stains which can be found in bathrooms or in kitchens, i.e., on stains containing mineral deposits like calcium and/or magnesium carbonate but also high amount of organic deposits such as greasy soap scum. Indeed, the presence of such greasy soap scum is detrimental to the limescale removal performance of acidic compositions.
- liquid acidic limescale removal compositions have been formulated that comprise on top of the acid, a surfactant to deliver effective cleaning on organic soils.
- a surfactant to deliver effective cleaning on organic soils.
- EP-A-496 188 discloses acidic compositions comprising maleic acid and nonionic surfactants for the cleaning of limescale-containing bathroom-type stains.
- limescale removal compositions with better performance in several respects including improved greasy soap scum cleaning performance and excellent limescale removal performance.
- an acidic liquid composition comprising an acid and a particular surfactant system, namely an amine oxide according to the formula R1R2R3NO, wherein each of R1, R2 and R3 is independently a saturated or unsaturated, substituted or unsubstituted, linear or branched alkyl group of from 1 to 30 carbon atoms, and an amine according to the formula RR'R''N, wherein R is a saturated or unsaturated, substituted or unsubstituted, linear or branched alkyl group of from 1 to 30 carbon atoms, and wherein R' and R'' are independently saturated or unsaturated, substituted or unsubstituted, linear or branched alkyl groups of from 1 to 30 carbon atoms or hydrogen.
- a particular surfactant system namely an amine oxide according to the formula R1R2R3NO, wherein each of R1, R2 and R3 is independently a saturated or unsaturated, substituted or unsubstituted, linear or branched
- compositions of the present invention comprising an acid, e.g., maleic acid alone or together with a second acid
- said surfactant system provides significantly improved greasy soap scum cleaning performance as well as improved limescale removal performance, as compared to the same compositions but with another surfactant, for example a nonionic surfactant, instead of said surfactant system, this even at a lower total surfactant level.
- the present invention also encompasses the use of an amine, as described herein, and/or of an amine oxide, as described herein, in an acidic liquid composition, to improve the greasy soap scum cleaning performance of said composition.
- EP-A-601 990 discloses an acidic composition
- an acidic composition comprising an acid for example maleic acid together with a thickening system comprising from 0.5% to 15% by weight of the total composition of a mixture of a nonionic surfactant and a cationic surfactant. No amine oxides or amines are disclosed.
- the compositions contain from 1% to 50% by weight of an amine oxide and an acidifying agent having a pKa of less than 6. No primary, secondary or tertiary amines are disclosed.
- GB 1 240 469 discloses a hard-surface cleaning composition which has a pH of not more than 7 and comprises (a) an inorganic or organic acid, or an acidic salts (5% to 95%), (b) a cationic surfactant (0.01% to 10%), and (c) a covalent compound other than (b) and which contains oxygen or a halogen and at least one hydrocarbon chain having at least four carbon atoms.
- the cationic surfactants disclosed are C8-24 amine oxides. No tertiary, secondary or primary amines are disclosed.
- Sulphamic acid is mentioned amongst the weak inorganic acids. No primary, secondary or tertiary amines are disclosed.
- GB 2 106 927 discloses liquid thickened toilet bowl cleaners comprising a non volatile water soluble organic acid, a surfactant (e.g., amine oxide), and a cellulose ether, said composition having a pH of 2.2 to 3.5. No primary, secondary or tertiary amines are disclosed.
- EP-A-253 676 discloses a thickened aqueous composition comprising at least one acidic salt, e.g., maleic acid (0.01%-30%), and a thickening agent (0.1% to 10%) which is at least one of the compounds selected from the group consisting of amine or amine oxide surfactants. No mixture of amine and amine oxide surfactants is expressly described, nor exemplified. EP-A-253 676 does not refer to the removal of limescale-containing stains like those found in bathrooms or in kitchens.
- the present invention is a liquid acidic composition
- a surfactant system comprising from 0.01% to 10% by weight of the total composition of an amine oxide according to the formula R1R2R3NO, wherein each of R1, R2 and R3 is independently a saturated or unsaturated, substituted or unsubstituted, linear or branched alkyl group of from 1 to 30 carbon atoms, and from 0.01% to 10% by weight of the total composition of an amine according to the formula RR'R''N, wherein R is a saturated or unsaturated, substituted or unsubstituted, linear or branched alkyl group of from 1 to 30 carbon atoms, and wherein R' and R'' are independently saturated or unsaturated, substituted or unsubstituted, linear or branched alkyl groups of from 1 to 30 carbon atoms, or hydrogen.
- the present invention also encompasses a process of treating hard-surfaces soiled by limescale-containing stains wherein an acidic liquid composition according to the present invention is applied in its neat form or in diluted form, onto said surfaces, then left to act onto said surfaces and then removed by rinsing.
- the present invention further encompasses the use, of a surfactant system comprising an amine oxide according to the formula R1R2R3NO, wherein each of R1, R2 and R3 is independently a saturated or unsaturated, substituted or unsubstituted, linear or branched alkyl group of from 1 to 30 carbon atoms, and/or an amine according to the formula RR'R''N, wherein R is a saturated or unsaturated, substituted or unsubstituted, linear or branched alkyl group of from 1 to 30 carbon atoms, and wherein R' and R'' are independently saturated or unsaturated, substituted or unsubstituted, linear or branched alkyl groups of from 1 to 30 carbon atoms, or hydrogen, in an acidic limescale removal composition, to improve the greasy soap scum cleaning performance of said composition.
- a surfactant system comprising an amine oxide according to the formula R1R2R3NO, wherein each of R1, R2 and R3
- compositions according to the present invention are designed for removing limescale deposits.
- they comprise as a first essential ingredient an acid.
- the acids to be used herein may be any inorganic or organic acid well-known to those skilled in the art, or mixtures thereof.
- Said compositions may comprise up to 80 % by weight of the total composition of said acid, or mixtures thereof.
- compositions of the present invention comprise maleic acid.
- the compositions according to the present invention comprise from 0.1% to 45% by weight of the total composition of maleic acid, preferably from 1% to 25% and more preferably from 8% to 20%. This percentage is calculated on the basis of the molecular weight of the acid form, but maleic anhydride is equally convenient for use in the compositions according to the present invention. Indeed maleic anhydride is generally cheaper and it is transformed into the acid form when incorporated in an aqueous medium.
- maleic acid is used alone as the acid of the acidic compositions of the present invention.
- a second acid is added on top of said maleic acid.
- Said second acid is desired to strengthen the limescale removal performance.
- the second acids to be used herein which are particularly efficient to remove limescale on many surfaces, have their first pKa not exceeding 5, more preferably not exceeding 3, and most preferably not exceeding 2.
- said acids can be organic or inorganic acids.
- Particularly suitable to be used herein are sulphonic acid derivatives including alkyl sulphonic acids and aryl sulphonic acids.
- Suitable aryl sulphonic acids for use herein are according to the formula : wherein R 1 , R 2 , R 3 , R 4 and R 5 are each H or SO 3 H, or linear or branched C 1 -C 4 alkyl chain; or mixtures thereof.
- Preferred acids having a first pKa not exceeding 5 to be used herein are sulphamic acid, sulphuric acid, aryl sulphonic acids, alkyl sulphonic acids, or mixtures thereof, more preferred are sulphamic acid, sulphuric acid, benzene sulphonic acid or mixtures thereof and highly preferred is sulphamic acid.
- compositions of the present invention comprise from 0.1% to 25% by weight of the total composition of a second acid which has a first pKa not exceeding 5, or mixtures thereof, preferably from 0.1% to 20%, more preferably from 0.1% to 10% and most preferably from 0.1% to 7%.
- compositions according to the present invention comprise as a second essential ingredient a surfactant system comprising an amine oxide, as described hereinafter, and an amine, as described hereinafter.
- Suitable amine oxides to be used herein are according to the following formula R 1 R 2 R 3 NO wherein each of R1, R2 and R3 is independently a saturated or unsaturated, substituted or unsubstituted, linear or branched alkyl groups of from 1 to 30 carbon atoms, and preferably of from 1 to 20 carbon atoms.
- Particularly preferred amine oxides to be used according to the present invention are amine oxides having the following formula R 1 R 2 R 3 NO wherein R1 is a saturated or unsaturated, substituted or unsubstituted, linear or branched alkyl group of 1 to 30 carbon atoms, preferably of 8 to 20 carbon atoms, more preferably of 6 to 16, most preferably of 8 to 14, and wherein R2 and R3 are independently substituted or unsubstituted, linear or branched alkyl groups of from 1 to 4 carbon atoms, preferably of from 1 to 3 carbon atoms, and more preferably are methyl groups, or mixtures thereof.
- Suitable amine oxides for use herein are for instance coconut dimethyl amine oxides, C12-C16 dimethyl amine oxides. Said amine oxides may be commercially available from Hoechst, Stephan, AKZO (under the trade name Aromox®) or FINA (under the trade name Radiamox®).
- compositions of the present invention comprise from 0.01% to 10% by weight of the total composition of said amine oxide, or mixtures thereof, preferably from 0.1% to 5% and more preferably from 0.1% to 3%.
- Suitable amines to be used herein are according to the following formula RR'R''N wherein R is a saturated or unsaturated, substituted or unsubstituted, linear or branched alkyl groups of from 1 to 30 carbon atoms, and preferably of from 1 to 20 carbon atoms and wherein R' and R'' are independently saturated or unsaturated, substituted or unsubstituted, linear or branched alkyl groups of from 1 to 30 carbon atoms or hydrogen.
- Particularly preferred amines to be used according to the present invention are amines having the following formula RR'R''N wherein R is a saturated or unsaturated, linear or branched alkyl group of 1 to 30 carbon atoms, preferably of 8 to 20 carbon atoms, more preferably of 6 to 16, most preferably of 8 to 14 and wherein R' and R'' are independently substituted or unsubstituted, linear or branched alkyl groups of from 1 to 4 carbon atoms, preferably of from 1 to 3 carbon atoms, and more preferably are methyl groups, or mixtures thereof.
- Suitable amines for use herein are for instance C12 dimethyl amine, coconut dimethyl amine, C12-C16 dimethyl amine. Said amines may be commercially available from Hoechst under the trade name Genamin®, AKZO under the trade name Aromox® or Fina under the trade name Radiamox®.
- compositions of the present invention comprise from 0.01% to 10% by weight of the total composition of said amine, or mixtures thereof, preferably from 0.1% to 5% and more preferably from 0.1% to 3%.
- the preferred liquid acidic compositions herein comprise said amine and said amine oxide in a weight ratio of said amine to said amine oxide of 10:1 to 1:10, preferably of 5:1 to 1:5 and most preferably of 1:1 to deliver optimum physical stability and optimum greasy soap scum cleaning.
- the surfactant system according to the present invention allows to lower the surface tension and to improve the wettability of the surfaces being cleaned with the liquid acidic compositions of the present invention.
- the presence of said surfactant system in the liquid acidic compositions of the present invention helps to solubilize the soils and to improve the streaking profile of the acids.
- an acidic liquid composition of the surfactant system according to the present invention, i.e., an amine oxide, as described herein, and an amine, as described herein, provides improved greasy soap scum cleaning performance as well as improved limescale removal performance, as compared to the greasy soap scum cleaning performance and limescale removal performance obtained with the same composition but with another surfactant like a nonionic surfactant, e.g. an alcohol ethoxylate (Dobanol® 91-8), instead of said surfactant system, this even at significantly lower total surfactant level.
- a nonionic surfactant e.g. an alcohol ethoxylate (Dobanol® 91-8
- the addition of an amine, as defined herein, and/or of an amine oxide, as defined herein, in a liquid acidic composition provides improved greasy soap scum cleaning performance, as compared to the same composition without any surfactant, or to the same composition but with another surfactant, e.g. a nonionic surfactant, this while providing excellent limescale removal performance.
- the present invention also encompasses the use, in an acidic liquid limescale removal composition, of a surfactant system comprising an amine, as defined herein, and/or an amine oxide, as defined herein, to improve the greasy soap scum cleaning performance of said composition.
- compositions according to the present invention are preferably aqueous. Accordingly, the compositions according to the present invention comprise from 10% to 95% by weight of the total composition of water, preferably from 50% to 90%, most preferably from 70% to 85%.
- compositions according to the present invention are liquid acidic compositions. Accordingly, the compositions according to the present invention have a pH as is below 3, preferably in the range of from 0.1 to 2.5, more preferably of from 0.1 to 2, and most preferably of from 0.3 to 1.5.
- the acidic liquid compositions of the present invention are physically stable, i.e. that no phase separation occurs when stored in rapid aging test (RAT) at 50 °C for 10 days or at 2 °C for 2 months.
- RAT rapid aging test
- compositions according to the present invention may further comprise a variety of other ingredients including other surfactants, colorants, bactericides, thickeners, dyes, chelants, pigments, solvents, stabilizers, perfumes, corrosion inhibitors and the like.
- compositions according to the present invention may further comprise other surfactants or mixtures thereof.
- the compositions according to the present invention may comprise up to 30% by weight of the total composition of said other surfactant or mixtures thereof on top of the surfactant system of the present invention, more preferably from 0.05% to 10%, more preferably from 0.1% to 8%, and most preferably from 0.1% to 3%.
- All types of surfactants may be used in the present invention including nonionic, anionic, cationic, amphoteric or zwitterionic surfactants. It is also possible to use mixtures of such surfactants without departing from the spirit of the present invention.
- Suitable nonionic surfactants to be used herein are alkoxylated alcohol nonionic surfactants which can be readily made by condensation processes which are well-known in the art. However, a great variety of such alkoxylated alcohols, especially ethoxylated and/or propoxylated alcohols is also conveniently commercially available. Surfactants catalogs are available which list a number of surfactants, including nonionics.
- preferred alkoxylated alcohols for use herein are nonionic surfactants according to the formula RO(E)e(P)pH where R is a hydrocarbon chain of from 2 to 24 carbon atoms, E is ethylene oxide and P is propylene oxide, and e and p which represent the average degree of, respectively ethoxylation and propoxylation, are of from 0 to 24.
- the hydrophobic moiety of the nonionic compound can be a primary or secondary, straight or branched alcohol having from 8 to 24 carbon atoms.
- Preferred nonionic surfactants for use in the compositions according to the invention are the condensation products of ethylene oxide with alcohols having a straight alkyl chain, having from 6 to 22 carbon atoms, wherein the degree of ethoxylation is from 1 to 15, preferably from 5 to 12.
- Such suitable nonionic surfactants are commercially available from Shell, for instance, under the trade name Dobanol® or from Shell under the trade name Lutensol® . These nonionics are preferred because they have been found to allow the formulation of a stable product without requiring the addition of stabilisers or hydrotopes. When using other nonionics, it may be necessary to add hydrotopes such as cumene sulphonate or solvents such as butyldiglycolether.
- Suitable anionic surfactants for use herein are according to the formula R 1 SO 3 M wherein R 1 represents a hydrocarbon group selected from the group consisting of straight or branched alkyl radicals containing from 6 to 24 carbon atoms and alkyl phenyl radicals containing from 6 to 15 carbon atoms in the alkyl group.
- M is a salt forming cation which typically is selected from the group consisting of sodium, potassium, ammonium, and mixtures thereof.
- Suitable anionic surfactants can be represented by the water-soluble salts of an alkyl sulfate or an alkyl polyethoxylate ether sulfate wherein the alkyl group contains from 6 to 24 carbon atoms, and preferably from 1 to 30 ethoxy groups for the alkyl polyethoxylate ether sulfates.
- Suitable cationic surfactants to be used herein include derivatives of quaternary ammonium, phosphonium, imidazolium and sulfonium compounds.
- Preferred cationic surfactants for use herein are according to the formula R 1 R 2 R 3 R 4 N + X - , wherein X is a counteranion, R 1 is a C 8 -C 20 hydrocarbon chain and R 2 , R 3 and R 4 are independently selected from H or C 1 -C 4 hydrocarbon chains.
- R 1 is a C 10 -C 18 hydrocarbon chain, most preferably C 12 , C 14, , or C 16
- R 2 , R 3 and R 4 are all three methyl
- X is halogen, preferably bromide or chloride, most preferably bromide.
- cationic surfactants are lauryl trimethyl ammonium bromide, stearyl trimethyl ammonium bromide (STAB), cetyl trimethyl ammonium bromide (CTAB) and myristyl trimethyl ammonium bromide (MTAB). Highly preferred herein are lauryl trimethyl ammonium salts.
- a cationic surfactant according to the formula R 1 R 2 R 3 R 4 N + X - , wherein X is a counteranion, R 1 is a C 8 -C 12 hydrocarbon chain and R 2 , R 3 and R 4 are independently selected from H or C 1 -C 4 hydrocarbon chains, and preferably of lauryl trimethyl ammonium salts, in a liquid acidic composition, allows to improve the limescale removal performance of said composition.
- another aspect of the present invention is the use of a cationic surfactant according to the formula R 1 R 2 R 3 R 4 N + X - , wherein X is a counteranion, R 1 is a C 8 -C 12 hydrocarbon chain and R 2 , R 3 and R 4 are independently selected from H or C 1 -C 4 hydrocarbon chains, preferably of lauryl trimethyl ammonium salts, in a liquid acidic composition, to improve the limescale removal performance of said composition.
- Suitable zwitterionic surfactants contain both cationic and anionic hydrophilic groups on the same molecule at a relatively wide range of pH's.
- the typical cationic group is a quaternary ammonium group, although other positively charged groups like phosphonium, imidazolium and sulfonium groups can be used.
- the typical anionic hydrophilic groups are carboxylates and sulfonates, although other groups like sulfates, phosphonates, and the like can be used.
- R 1 -N + (R 2 )(R 3 )R 4 X - wherein R 1 is a hydrophobic group; R 2 and R 3 are each C 1 -C 4 alkyl, hydroxy alkyl or other substituted alkyl group which can also be joined to form ring structures with the N; R 4 is a moiety joining the cationic nitrogen atom to the hydrophilic group and is typically an alkylene, hydroxy alkylene, or polyalkoxy group containing from 1 to 4 carbon atoms; and X is the hydrophilic group which is preferably a carboxylate or sulfonate group.
- Preferred hydrophobic groups R 1 are alkyl groups containing from 8 to 22, preferably less than 18, more preferably less than 16 carbon atoms.
- the hydrophobic group can contain unsaturation and/or substituents and/or linking groups such as aryl groups, amido groups, ester groups and the like.
- the simple alkyl groups are preferred for cost and stability reasons.
- each R 2 is either a hydrogen (when attached to the amido nitrogen), short chain alkyl or substituted alkyl containing from one to 4 carbon atoms, preferably groups selected from the group consisting of methyl, ethyl, propyl, hydroxy substituted ethyl or propyl and mixtures thereof, preferably methyl
- each R 3 is selected from the group consisting of hydrogen and hydroxy groups and each n is a number from 1 to 4, preferably from 2 to 3, more preferably 3, with no more than one hydroxy group in any (C(R 3 ) 2 ) moiety.
- the R 1 groups can be branched and/or unsaturated.
- R 2 groups can also be connected to form ring structures.
- a surfactant of this type is a C 10 -C 14 fatty acylamidopropylene(hydroxypropylene)sulfobetaine that is available from the Sherex Company under the trade name "Varion CAS sulfobetaine”®.
- Suitable amphoteric surfactants are surfactants which are similar to the zwitterionic surfactants but without the quaternary group. However, they contain an amine group that is protonated at the low pH of the composition to form cationic group and they may also possess an anionic group at these pHs.
- compositions according to the present invention are particularly suitable for treating hard-surfaces soiled by limescale-containing stains.
- limescale-containing stains it is meant herein any pure limescale stains, i.e., any stains composed essentially of mineral deposits as well as limescale-containing stains typically found, for example, in a kitchen or in a bathroom, i.e., stains which contain not only mineral deposits like calcium and/or magnesium carbonate but also soap scum (e.g., calcium stearate) and grease.
- compositions of the present invention exhibit excellent limescale removing performance when used to treat any types of surfaces soiled by limescale-containing stains comprising not only pure limescale deposits but also at least 10% by weight of the total stain of organic deposits like soap scum and grease, preferably more than 30%.
- surfaces can be found in bathrooms, kitchens, but also in appliances including large appliances such as automatic dish washers and/or washing machines.
- the present invention encompasses a process of treating hard-surfaces soiled by limescale-containing stains wherein an aqueous acidic liquid composition according to the present invention is applied in its neat form or in diluted form, onto said surfaces, then left to act onto said surfaces and then removed by rinsing.
- the expression "used in diluted form” herein includes dilution by the user. Typical dilution levels are of from 0.5% to 50% by weight of the composition.
- treating includes removing limescale deposits while being safe to the surfaces treated as well as cleaning greasy soap scum stains due to the presence of said surfactant system.
- compositions I II III IV V VI Maleic acid 10 -- 7 2 10 8 Sulphamic acid 2 10 1 4 -- -- Citric acid -- -- -- -- 2 -- C12 dimethyl amine 0.5 -- -- 0.8 -- -- coconut dimethyl amine -- 0.4 -- -- 1 -- C12-C16 dimethyl amine -- -- 0.5 -- -- -- -- coconut dimethyl amine oxide 0.5 0.4 -- -- 0.5 1 C12-C16 dimethyl amine oxide -- -- 0.5 0.4 -- -- -- C8 dimethyl amine -- -- -- -- -- -- -- 1 LTAB* -- -- 0.5 -- -- 0.4 Waters & Minors -------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
- compositions of the above examples exhibit excellent limescale removal performance as well as outstanding greasy soap scum cleaning performance when used to clean limescale-containing stains found in a kitchen and in a bathroom, this both when used neat or in diluted form.
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Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP96201366A EP0808891A1 (de) | 1996-05-21 | 1996-05-21 | Saure Reinigungszusammensetzungen |
JP9542586A JPH11514696A (ja) | 1996-05-21 | 1997-05-16 | 酸性クリーニング組成物 |
PCT/US1997/008353 WO1997044421A1 (en) | 1996-05-21 | 1997-05-16 | Acidic cleaning compositions |
CA 2255722 CA2255722A1 (en) | 1996-05-21 | 1997-05-16 | Acidic cleaning compositions |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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EP96201366A EP0808891A1 (de) | 1996-05-21 | 1996-05-21 | Saure Reinigungszusammensetzungen |
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EP0808891A1 true EP0808891A1 (de) | 1997-11-26 |
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EP96201366A Withdrawn EP0808891A1 (de) | 1996-05-21 | 1996-05-21 | Saure Reinigungszusammensetzungen |
Country Status (4)
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EP (1) | EP0808891A1 (de) |
JP (1) | JPH11514696A (de) |
CA (1) | CA2255722A1 (de) |
WO (1) | WO1997044421A1 (de) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2011104000A1 (en) * | 2010-02-24 | 2011-09-01 | Clariant International Ltd | Use of n,n-bis(2-hydroxyethyl)cocoamine oxide for the cleaning of hard surfaces |
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JP5637586B2 (ja) * | 2010-04-22 | 2014-12-10 | ライオン株式会社 | 硬質表面用液体洗浄剤組成物 |
JP2012017420A (ja) * | 2010-07-08 | 2012-01-26 | Neos Co Ltd | 水溶性洗浄剤組成物 |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2071688A (en) * | 1980-03-13 | 1981-09-23 | Jeyes Ltd | Liquid Cleaning and Descaling Compositions |
EP0253676A2 (de) * | 1986-07-17 | 1988-01-20 | R & C PRODUCTS PTY. LIMITED | Aminsäure-Verdickungsmittel |
EP0666305A1 (de) * | 1994-02-03 | 1995-08-09 | The Procter & Gamble Company | Saure Reinigungszusammensetzungen |
EP0666304A1 (de) * | 1994-02-03 | 1995-08-09 | The Procter & Gamble Company | Saure Reinigungszusammensetzungen |
EP0666303A1 (de) * | 1994-02-03 | 1995-08-09 | The Procter & Gamble Company | Zusammensetzungen zum Entfernen von Kesselstein |
WO1995033024A1 (en) * | 1994-05-31 | 1995-12-07 | The Procter & Gamble Company | Cleaning compositions |
WO1996013565A1 (en) * | 1994-10-28 | 1996-05-09 | The Procter & Gamble Company | Hard surface cleaning compositions comprising protonated amines and amine oxide surfactants |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
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US4195077A (en) * | 1974-01-18 | 1980-03-25 | The Procter & Gamble Company | Detergent compositions comprising modified proteins |
CA1104451A (en) * | 1978-02-28 | 1981-07-07 | Manuel Juan De Luque | Detergent bleach composition and process |
US4963226A (en) * | 1989-01-23 | 1990-10-16 | The Procter & Gamble Company | Process for spray-drying detergent compositions |
US5364551A (en) * | 1993-09-17 | 1994-11-15 | Ecolab Inc. | Reduced misting oven cleaner |
-
1996
- 1996-05-21 EP EP96201366A patent/EP0808891A1/de not_active Withdrawn
-
1997
- 1997-05-16 CA CA 2255722 patent/CA2255722A1/en not_active Abandoned
- 1997-05-16 WO PCT/US1997/008353 patent/WO1997044421A1/en active Application Filing
- 1997-05-16 JP JP9542586A patent/JPH11514696A/ja active Pending
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2071688A (en) * | 1980-03-13 | 1981-09-23 | Jeyes Ltd | Liquid Cleaning and Descaling Compositions |
EP0253676A2 (de) * | 1986-07-17 | 1988-01-20 | R & C PRODUCTS PTY. LIMITED | Aminsäure-Verdickungsmittel |
EP0666305A1 (de) * | 1994-02-03 | 1995-08-09 | The Procter & Gamble Company | Saure Reinigungszusammensetzungen |
EP0666304A1 (de) * | 1994-02-03 | 1995-08-09 | The Procter & Gamble Company | Saure Reinigungszusammensetzungen |
EP0666303A1 (de) * | 1994-02-03 | 1995-08-09 | The Procter & Gamble Company | Zusammensetzungen zum Entfernen von Kesselstein |
WO1995033024A1 (en) * | 1994-05-31 | 1995-12-07 | The Procter & Gamble Company | Cleaning compositions |
WO1996013565A1 (en) * | 1994-10-28 | 1996-05-09 | The Procter & Gamble Company | Hard surface cleaning compositions comprising protonated amines and amine oxide surfactants |
Non-Patent Citations (1)
Title |
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ROERIG, H. ET AL: "Cationic surfactants in organic acid-based hard surface cleaners", COMUN. JORN. COM. ESP. DETERG., vol. 21, 1990, SEVILLA ES, pages 191 - 206, XP000196765 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011104000A1 (en) * | 2010-02-24 | 2011-09-01 | Clariant International Ltd | Use of n,n-bis(2-hydroxyethyl)cocoamine oxide for the cleaning of hard surfaces |
Also Published As
Publication number | Publication date |
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CA2255722A1 (en) | 1997-11-27 |
WO1997044421A1 (en) | 1997-11-27 |
JPH11514696A (ja) | 1999-12-14 |
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