US3042621A - Detergent composition - Google Patents
Detergent composition Download PDFInfo
- Publication number
- US3042621A US3042621A US693801A US69380157A US3042621A US 3042621 A US3042621 A US 3042621A US 693801 A US693801 A US 693801A US 69380157 A US69380157 A US 69380157A US 3042621 A US3042621 A US 3042621A
- Authority
- US
- United States
- Prior art keywords
- water
- acidic
- alkaline
- acid
- soluble
- 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.)
- Expired - Lifetime
Links
- 239000003599 detergent Substances 0.000 title claims description 70
- 239000000203 mixture Substances 0.000 title claims description 64
- 230000002378 acidificating effect Effects 0.000 claims description 62
- 239000011248 coating agent Substances 0.000 claims description 35
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 34
- 239000000463 material Substances 0.000 claims description 32
- 238000000576 coating method Methods 0.000 claims description 22
- 230000007935 neutral effect Effects 0.000 claims description 20
- 238000004140 cleaning Methods 0.000 claims description 19
- 150000007513 acids Chemical class 0.000 claims description 8
- 239000000243 solution Substances 0.000 description 35
- 239000004615 ingredient Substances 0.000 description 32
- 239000002253 acid Substances 0.000 description 22
- 239000000047 product Substances 0.000 description 22
- 239000002245 particle Substances 0.000 description 20
- 235000014113 dietary fatty acids Nutrition 0.000 description 16
- 239000000194 fatty acid Substances 0.000 description 16
- 229930195729 fatty acid Natural products 0.000 description 16
- -1 fatty alcohol sulfate Chemical class 0.000 description 16
- 150000004665 fatty acids Chemical class 0.000 description 15
- 150000003839 salts Chemical class 0.000 description 14
- 239000007787 solid Substances 0.000 description 14
- 239000007844 bleaching agent Substances 0.000 description 9
- 230000001747 exhibiting effect Effects 0.000 description 9
- 125000000129 anionic group Chemical group 0.000 description 8
- 239000011734 sodium Substances 0.000 description 8
- 229910052708 sodium Inorganic materials 0.000 description 8
- 235000013162 Cocos nucifera Nutrition 0.000 description 7
- 244000060011 Cocos nucifera Species 0.000 description 7
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 7
- 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 7
- 238000000034 method Methods 0.000 description 7
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 7
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 230000008859 change Effects 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000011973 solid acid Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
- 238000004061 bleaching Methods 0.000 description 4
- 125000002091 cationic group Chemical group 0.000 description 4
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 4
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 4
- 239000002304 perfume Substances 0.000 description 4
- 239000000344 soap Substances 0.000 description 4
- 229960001922 sodium perborate Drugs 0.000 description 4
- 229910052938 sodium sulfate Inorganic materials 0.000 description 4
- 235000011152 sodium sulphate Nutrition 0.000 description 4
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- QZXSMBBFBXPQHI-UHFFFAOYSA-N N-(dodecanoyl)ethanolamine Chemical compound CCCCCCCCCCCC(=O)NCCO QZXSMBBFBXPQHI-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000004115 Sodium Silicate Substances 0.000 description 3
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 239000008240 homogeneous mixture Substances 0.000 description 3
- 229910017053 inorganic salt Inorganic materials 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 3
- 239000003380 propellant Substances 0.000 description 3
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 3
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 3
- 229910052911 sodium silicate Inorganic materials 0.000 description 3
- 235000019832 sodium triphosphate Nutrition 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 239000005639 Lauric acid Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 239000003929 acidic solution Substances 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 229940077388 benzenesulfonate Drugs 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 229960000541 cetyl alcohol Drugs 0.000 description 2
- YMKDRGPMQRFJGP-UHFFFAOYSA-M cetylpyridinium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 YMKDRGPMQRFJGP-UHFFFAOYSA-M 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 239000003240 coconut oil Substances 0.000 description 2
- 235000019864 coconut oil Nutrition 0.000 description 2
- 230000003750 conditioning effect Effects 0.000 description 2
- 230000000994 depressogenic effect Effects 0.000 description 2
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 2
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- ILRSCQWREDREME-UHFFFAOYSA-N dodecanamide Chemical class CCCCCCCCCCCC(N)=O ILRSCQWREDREME-UHFFFAOYSA-N 0.000 description 2
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 2
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 159000000011 group IA salts Chemical class 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- SUMDYPCJJOFFON-UHFFFAOYSA-N isethionic acid Chemical compound OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 description 2
- 239000011344 liquid material Substances 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 239000002453 shampoo Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 description 2
- 229910000342 sodium bisulfate Inorganic materials 0.000 description 2
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 2
- 235000019795 sodium metasilicate Nutrition 0.000 description 2
- 238000001694 spray drying Methods 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 239000003784 tall oil Substances 0.000 description 2
- 239000003760 tallow Substances 0.000 description 2
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 2
- WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- YRIZYWQGELRKNT-UHFFFAOYSA-N 1,3,5-trichloro-1,3,5-triazinane-2,4,6-trione Chemical compound ClN1C(=O)N(Cl)C(=O)N(Cl)C1=O YRIZYWQGELRKNT-UHFFFAOYSA-N 0.000 description 1
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N 1-Tetradecanol Natural products CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 1
- BHNZEZWIUMJCGF-UHFFFAOYSA-N 1-chloro-1,1-difluoroethane Chemical compound CC(F)(F)Cl BHNZEZWIUMJCGF-UHFFFAOYSA-N 0.000 description 1
- VJYAJQFKKLYARJ-UHFFFAOYSA-N 2-[2-[2-[2-[2-[2-[2-[2-[2-[4-(2,4,4-trimethylpentan-2-yl)phenoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCOCCOCCOCCOCCOCCOCCOCCOCCO)C=C1 VJYAJQFKKLYARJ-UHFFFAOYSA-N 0.000 description 1
- OLQIKGSZDTXODA-UHFFFAOYSA-N 4-[3-(4-hydroxy-2-methylphenyl)-1,1-dioxo-2,1$l^{6}-benzoxathiol-3-yl]-3-methylphenol Chemical compound CC1=CC(O)=CC=C1C1(C=2C(=CC(O)=CC=2)C)C2=CC=CC=C2S(=O)(=O)O1 OLQIKGSZDTXODA-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 239000004338 Dichlorodifluoromethane Substances 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical class CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
- 241000243251 Hydra Species 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 235000021360 Myristic acid Nutrition 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- OTGQIQQTPXJQRG-UHFFFAOYSA-N N-(octadecanoyl)ethanolamine Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCO OTGQIQQTPXJQRG-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- BELBBZDIHDAJOR-UHFFFAOYSA-N Phenolsulfonephthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2S(=O)(=O)O1 BELBBZDIHDAJOR-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical class OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 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
- 229910000318 alkali metal phosphate Inorganic materials 0.000 description 1
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 230000002421 anti-septic effect Effects 0.000 description 1
- 229940027983 antiseptic and disinfectant quaternary ammonium compound Drugs 0.000 description 1
- 229940064004 antiseptic throat preparations Drugs 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 235000010338 boric acid Nutrition 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229960001927 cetylpyridinium chloride Drugs 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- VDQQXEISLMTGAB-UHFFFAOYSA-N chloramine T Chemical compound [Na+].CC1=CC=C(S(=O)(=O)[N-]Cl)C=C1 VDQQXEISLMTGAB-UHFFFAOYSA-N 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- CEJLBZWIKQJOAT-UHFFFAOYSA-N dichloroisocyanuric acid Chemical compound ClN1C(=O)NC(=O)N(Cl)C1=O CEJLBZWIKQJOAT-UHFFFAOYSA-N 0.000 description 1
- GXGAKHNRMVGRPK-UHFFFAOYSA-N dimagnesium;dioxido-bis[[oxido(oxo)silyl]oxy]silane Chemical compound [Mg+2].[Mg+2].[O-][Si](=O)O[Si]([O-])([O-])O[Si]([O-])=O GXGAKHNRMVGRPK-UHFFFAOYSA-N 0.000 description 1
- 238000004851 dishwashing Methods 0.000 description 1
- JVOYGBUYQTYMEZ-UHFFFAOYSA-N dodecanamide;sodium Chemical compound [Na].CCCCCCCCCCCC(N)=O JVOYGBUYQTYMEZ-UHFFFAOYSA-N 0.000 description 1
- 238000002036 drum drying Methods 0.000 description 1
- 238000007580 dry-mixing Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 239000003974 emollient agent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 239000007850 fluorescent dye Substances 0.000 description 1
- 230000002070 germicidal effect Effects 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- WJRBRSLFGCUECM-UHFFFAOYSA-N hydantoin Chemical compound O=C1CNC(=O)N1 WJRBRSLFGCUECM-UHFFFAOYSA-N 0.000 description 1
- 229940091173 hydantoin Drugs 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052816 inorganic phosphate Inorganic materials 0.000 description 1
- 229940045996 isethionic acid Drugs 0.000 description 1
- QRXWMOHMRWLFEY-UHFFFAOYSA-N isoniazide Chemical compound NNC(=O)C1=CC=NC=C1 QRXWMOHMRWLFEY-UHFFFAOYSA-N 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 238000004900 laundering Methods 0.000 description 1
- 239000006193 liquid solution Substances 0.000 description 1
- LWXVCCOAQYNXNX-UHFFFAOYSA-N lithium hypochlorite Chemical class [Li+].Cl[O-] LWXVCCOAQYNXNX-UHFFFAOYSA-N 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229940099273 magnesium trisilicate Drugs 0.000 description 1
- 229910000386 magnesium trisilicate Inorganic materials 0.000 description 1
- 235000019793 magnesium trisilicate Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical class C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- STZCRXQWRGQSJD-GEEYTBSJSA-M methyl orange Chemical compound [Na+].C1=CC(N(C)C)=CC=C1\N=N\C1=CC=C(S([O-])(=O)=O)C=C1 STZCRXQWRGQSJD-GEEYTBSJSA-M 0.000 description 1
- 229940012189 methyl orange Drugs 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229940043348 myristyl alcohol Drugs 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 239000003346 palm kernel oil Substances 0.000 description 1
- 235000019865 palm kernel oil Nutrition 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- TWBKZBJAVASNII-UHFFFAOYSA-N pentadecane-1-sulfonic acid Chemical class CCCCCCCCCCCCCCCS(O)(=O)=O TWBKZBJAVASNII-UHFFFAOYSA-N 0.000 description 1
- 125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229960003531 phenolsulfonphthalein Drugs 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000012254 powdered material Substances 0.000 description 1
- 150000003140 primary amides Chemical class 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- RLJSXMVTLMHXJS-UHFFFAOYSA-M sodium;4-decylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCC1=CC=C(S([O-])(=O)=O)C=C1 RLJSXMVTLMHXJS-UHFFFAOYSA-M 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 229940012831 stearyl alcohol Drugs 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid group Chemical group S(N)(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 229960003080 taurine Drugs 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 235000019801 trisodium phosphate Nutrition 0.000 description 1
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000009736 wetting Methods 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
- C11D3/40—Dyes ; Pigments
-
- 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
- C11D17/0039—Coated compositions or coated components in the compositions, (micro)capsules
-
- 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
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/02—Inorganic compounds
- C11D7/04—Water-soluble compounds
- C11D7/08—Acids
Definitions
- the present invention relates to an essentially nonabrasive detergent composition exhibiting substantially non-acidic and acidic pH conditions in a predetermined order of succession in water, and to a process of preparing the same, as hereinafter described and claimed.
- the optimum effectiveness of detergent compositions for different functions or properties may occur at different pH ranges in water.
- a detergent composition exhibiting an alkaline pH in water may be preferable for various cleaning operations whereas a composition exhibiting an acidic pH may be desired for other cleaning or related operations or for conditioning of the cleaned material.
- Such practice could be utilized in many fields of application including commercial laundry, textile-treating and hair-treating operations and the like.
- a detergent composition exhibiting'variable and controlled pH conditions in water which comprises 'an ingredient yielding in solution an alkaline or substantially neutral pH condition, and an ingredient adapted to convert the solution to an acidic pH condition after elapse of a predetermined time.
- a non-abrasive cleaning composition in particulate form which upon admixture with water is adapted to yield an alkaline or neutral pH condition and an acidic pH condition successively to the resulting cleaning solution which comprises essentially a mixture of a Water-soluble organic neutral or alkaline detergent, and a water-soluble acidic ingredient which is adapted to dissolve in' an amount sufficient to subsequently convert said cleaning solution to an acidic pH condition, said acidic ingredient having a coating of a water-dispersible material to retard its rate of solubility.
- a preferred embodiment comprises a particulate mixture of an organic detergent, a water-soluble alkaline builder salt and a normally solid water-soluble acid having a coating of a water-dispersible material on the acid particles.
- compositions yielding successive alkaline and acidic pH conditions are within the scope of the invention.
- pH conditions in the specification and claims it is intended that such condition be illustrated by a 0.25% solution position in water.
- the composition should contain a water-soluble organic substantially neutral or alkaline detergent.
- a water-soluble organic substantially neutral or alkaline detergent Such compositions are known and are disclosed in Us. Patent of the detergent com- :No. 2,625,513, issued January .13, 1953. It is highly advantageous to incorporate an organic detergent material such as the organic anionic and non-ionic surface-active agents for a variety of effects including detergency, foaming, and surface tension and wetting effects so as tofacilitate removal of the dispersible coating on the acidic par- -to 50 alkylene oxide groups.
- the soaps are generally the water-soluble salts of higher fatty acids (including rosin acids) which are derived usually from fats, oils and waxes of animal, vegetable or marine origin, e.g. tallow, coconut oil, tall oil, palm kernel oil soaps and the like. It is preferred to employ a higher alkyl aryl sulfonate such as an alkyl benzene sulfonate detergent wherein the alkyl group has about 8 to 16 carbon atoms.
- higher aryl sulfonate such as an alkyl benzene sulfonate detergent wherein the alkyl group has about 8 to 16 carbon atoms.
- Suitable examples are sodium decyl benzene sulfonate, sodium dodecyl and pentadecyl sulfonates wherein the dodecyl and pentadecyl groups are derived from a propylene polymer, and sodium keryl benzene sulfonate.
- Other suitable agents are the surface-active sulfated or sulfonated aliphatic compounds, preferably having 8 to 22 carbon atoms. Examples thereof are sulfuric acid esters of polyhydric alcohols incompletely esterified with higher fatty acids (e.g. sodium coconut oil monoglyceride monosulfate); the long-chain pure or mixed higher alkyl sulfates (e.g.
- anionic surface-active agents are used generally in the form of their water-soluble salts, such as the alkali metal (e.g. sodium, potassium), though other soluble salts such as ammonium, alkylolamine and alkaline earth metal salts may be used if desired depending upon the particular detergent.
- alkali metal e.g. sodium, potassium
- other soluble salts such as ammonium, alkylolamine and alkaline earth metal salts may be used if desired depending upon the particular detergent.
- non-ionic agents such as the non-ionic polyalkylene oxide condensates with an aliphatic or aromatic hydrophobic group.
- the hydrophobic organic group contains usually at least about 8 carbons condensed with at least about 5 and usually up
- examples are the polyethylene oxide condensates with alkyl phenols having 6 to 20 carbons in the alkyl group such as Igepal CA and CO; the polyethylene oxide esters with higher fatty acids such as tall oil acids or lauric acid condensed with about 16 or 20 ethylene oxide groups; the polyethylene oxide condensates with higher aliphatic alcohols such as lauryl, myristyl, oleyl or stearyl alcohol with 6 to 30 moles ethylene oxide; the polyoxyethylene oxide condensates with higher fatty acid amides such as coconut fatty acid amide containing about 10 to 50 moles ethylene oxide.
- the water-soluble polyoxyethylene condensates With hydrophobic polyoxypropylene glycols may be employed also.
- any Water-soluble ingredient which yields an alkaline pH of above "7, preferably a pH of 8 to 12, to the aqueous solution may be employed in the composition also.
- the alkaline organic detergents such as the water-soluble soaps and the like described above may be employed but it is' preferred to use the water-soluble inorganic alkaline builder salts, such as the alkali metal carbonates (e.g. sodium carbonate), the alkali metal phosphates (e.g. trisodium phosphate, tetrasodium pyrophosphate, sodium tripolyphosphate), the alkali metal silicates (eg. sodium metasilicate) and the alkali metal borates (e.g. sodium borate).
- the alkali metal carbonates e.g. sodium carbonate
- the alkali metal phosphates e.g. trisodium phosphate, tetrasodium pyrophosphate, sodium tripolyphosphate
- Any suitable base such as sodium and potassium hydroxide, and tetramethylammonium hydroxide may be employed also.
- a normally solid organic detergent and alkaline builder salts and bases but, if desired, 'a normally'liquid mate rial may be employed by suitable combination with a Solid carrier such as by adsorption of a liquid. detergent upon a solid alkaline builder, and the like.
- the concentration of these active ingredients and mixtures thereof in the detergent compositions of the present invention vary widely according to the contemplated field of application and any amount of the detersive material may be employed which does not substantially adversely affect the desired characteristics of the product.
- the neutral or alkaline detergent may be present in amounts from about /2 to about 99%, and preferably from about 1 to 75 by weight of total solids.
- the composition may be free from alkaline inorganic builder salts if desired.
- a preferred formulation comprises a mixture of about 5 to 50% neutral or alkaline organic detergent with the balance of total solids being primarily water-soluble inorganic salts, preferably containing about 5 to 75% alkaline builders such as phosphates, which is admixed With a sufficient amount of an acidic ingredient as hereinafter described.
- the neutral and alkaline detersive materials may be employed in the form of solid particles of any suitable size.
- the particle size is not critical but will vary usually from about to 400 mesh as determined on a U.S. standard sieve.
- the organic detergent and alkaline builder salts and the like may be in individual particulate form or they may be admixed in any suitable way to prepare mixed granules.
- the organic detergent and alkaline salts in the form of an aqueous slurry may be subjected to the usual drying procedures in order to obtain a relatively dry, homogeneous granular product, such as by heat-drying (e.g. drum-drying or spray-drying) of the mixture in known manner. 7
- Any water-soluble acidic ingredient which will dissolve in the cleansing solution to yield an acidic pH of below 7, preferably a pH from 2 to 7, to the aqueous solution may be employed in the product.
- a normally solid acid or acid salt in particulate form.
- a normally liquid material may be employed by suitable combination with a solid carrier in particulate form, such as diatomaceous earth or bentonite.
- the particle size of the acidic material is not critical and it may be employed in any suitable size as illustrated for the detersive materials above.
- Suitable materials are the organic acids such as tartaric acid, maleic acid, boric acid, glutamic acid, citric acid, acetic acid, oxalic acid, gluconic acid and its lactone, and the like.
- Suitable inorganic acids and acid salts such as sulfamic and phosphoric acids and sodium bisulfate may be employed also.
- the acidic ingredient should be used in any amount sufficient to convert the substantially neutral or alkaline solution to an acidic solution of less than 7 and preferably to a pH from about 2 to 5, when the quantity of acid has been dissolved or otherwise released in the cleansing solution.
- the amount of acid be from about /2 to 50% and preferably from about 1 to by weight.
- the two materials tend to neutralize one another such that the cleansing solution will have either an alkaline or an acidic pH condition depending upon the proportion and strentgh of the different ingredients.
- the composition would yield initially an acidic condition.
- it is necessary to defer or retard the rate of solubility of the acidic ingredient. This deferred acidification permits the user to utilize initially the alkaline or neutral properties of the product for optimum foaming and cleaning effects in many cases followed by use of the acidic properties of the product for other optimum effects in rinsing, dyeing, bleaching and conditioning of the cleansed material.
- the rate of solution of the acidic constituent is to be sufiiciently depressed to permit the neutral or alkaline detersive materials to dissolve first and thereby permit utilization of these properties.
- the acidic constituent must then be present in sufiicient amount or in stoichiometric excess over the alkaline ingredient so that when it is dissolved or released after a predetermined time the pH of the cleansing solution is reduced to the desired acidic level.
- the rate of solubility of the acidic constituent may be reduced in any suitable manner. It is preferred to coat the normally solid acid particles with a solution inhibitor such as a water-dispersible coating agent. The presence of such a film or coating upon the particles of the acid will inhibit and retard the solubility of the acid when the composition is admixed with water initially.
- the amount of the coating is not critical and may vary from a monomolecular film to a coating of any particular size depending upon the specific coating agent, its water-dispersibility, the contemplated conditions of use, and the particular time interval which is desired before the change in the pH condition of the aqueous cleaning solution.
- the predetermined time interval for the pH change may be controlled so as to be a few seconds up to any point desired in the use of the product such as up to about 30 minutes. It is preferred that the change in pH occur from about 15 seconds to 15 minutes after the product is admixed in water.
- any suitable material may be used as the coating agent such as the higher fatty alcohols, preferably having 12 to 18 carbon atoms (e.g. lauryl alcohol, coconut fatty alcohol, cetyl alcohol, stearyl alcohol), mineral oil, the higher fatty acid amide compounds, preferably having 12 to 18 carbon atoms in the acyl radical (lauric acid, coconut acid and myristic acid primary amides and the corresponding monoethanolamides, isopropanolamides and diethanolamides) and their ethylene oxide reaction products having up to about 5 moles of ethylene oxide, the higher fatty acids, preferably having 12 to 18 carbons, such as stearic acid, palmitic acid, tallow fatty acids and the like.
- the higher fatty acids preferably having 12 to 18 carbons
- the higher fatty acids preferably having 12 to 18 carbons, such as stearic acid, palmitic acid, tallow fatty acids and the like.
- coating materials are the waxlike polymers of ethylene glycol such as Oarbowax 1500, 2025 and 4000, the soluble starches and dextrins and the like. These materials may have highly limited solubility in water to extreme solubility but are effective to delay the solubility or release of the acid in the cleansing solution.
- the term waterdispersi ble coating agent or equivalent as used herein refers to agents of varying water solubility or dispersibility but which have been found to be dispersed or dissolve under conditions of use of the product.
- organic materials such as lauryl alcohol and lauric acid amides and alkylol-amides have limited water solubility but in the presence of organic detergent material tend to dissolve in the cleansing solution.
- the coating agent may be applied to the particles of the acid in any suitable manner. It is preferred that the coating agent be dissolved, suspended or dispersed in an appropriate solvent or heated to molten form and then sprayed or atomized on the individual acid particles to form the desired coating.
- Any suitable solvent may be employed, such as a normally gaseous propellant in a pressure container. Examples are the normally gaseous low-molecular weight hydrocarbon and halogenated hydrocarbon propellants, such as propane, butane, halogenated ethanes and methanes.
- the propellants known as the Freons and Genetrons are suitable, examples being dichlorodifluoromethane and monochlorodifluoroethane.
- solvents or dispersing mediums such as ethanol, isopropanol and aqueous alcohol mixtures may be suitably employed also.
- the desired coating or film on the surface of the minor proportion usually such as from about A acid particles.
- the coating agent is normally solid it will dry to a film, and where it is normally liquid it will be adsorbed or absorbed upon the surfaces of the particles.
- the coating material may be applied also in solid form to the surfaces of the acid particles by mixing the coating agent in powdered form with the acid particles by suitable means for mechanical admixture including tumbling in a rotary drum.
- the various ingredients such as the detergent, alkaline builder salt and the coated acidic ingredient are mixed in particulate form to produce a dry, uniform granular mixture.
- the ingredients are admixed mechanically by tumbling, fluidizing or the like in conventional soap powder mixers known in the art or by any other suitable means for mechanical admixture.
- the organic detergent and watersoluble alkaline ingredients dissolve to form a non-acidic solution. Since the acid particles are coated with higher fatty acid amide or any other suitable coating as indicated, its rate of solution is sufficiently depressed to permit the alkaline builder to dissolve first. After a predetermined time, which may be controlled as desired by selection of the particular coating agent, the coating material disperses in the aqueous medium whereupon the acid is released and dissolves so that the pH is reduced to the desired acidic condition.
- the product may contain a bleaching agent which results in effective bleaching action during use of the product.
- the bleaching agent may be incorporated into the product in any suitable manner, such as during or after the mixing of the essential ingredients. In general, bleaching agents are more effective in one pH condition than another. Since the product during use will form a plurality of controlled pH conditions, there can be obtained at some stage optimum conditions for a particular bleaching agent.
- the bleaching agent may be incorporated into the detergent composition in known manner, such as by dry mixing of the powdered materials or in any other suitable manner. If desired, the bleaching agent may be coated with any suitable material such as the coating agents previously described so that the bleaching agent is released in the same manner. Examples of suitable bleaching agents are the known oxygen and chlorine-releasing substances, such as sodium perborate, sodium, calcium and lithium hypochlorites, dichlorocyanuric acid, trichlorocyanuric acid,
- Chloramine T diohlorodimethyl hydantoin and the like.
- the amount of bleaching agent is not critical but will he usually from about 0.01 to 50% of the product (e.g.
- a cationic surface-active agent may be incorporated in the product also. It may be admixed in powdered or liquid form with the ingredients in any suitable manner. Vfnere it is desired to use a cationic agent, it is preferred to admix it with the acidic ingredient and coatthis mixture with the coating agent.
- Suitable cationic detergents are the higher alkyl quaternary ammonium compounds such as the cetyl quaternary ammonium salts. Specific examples of such materials are cetyl trimethy-l ammonium chloride, cetyl pyridinium chloride, and the like. These materials are employed in to 25% of the composition.
- a suitable color indicator which would demonstrate to the consumer'whenthe change from one pH condition to the other pH condition occurs or when a particular pH level is obtained during use may be incorpoorated in the product also.
- the quantity of indicator is not critical except that it should be capable of producing a detectable coloration to the cleansing solution. in general, the amount of color indicator vary with the type of indicator but is usually from about 5' parts per million to 3% of the product. If methyl orange is employed, the color of the aqueous solution is yellow when the alkaline ingredient dissolves initially and the acid is coated, but the cleaning solution turns red when the acid dissolves in a stoichiometric excess after elapse of a predetermined time.
- Another suitable color indicator is bromo t-hymol blue which changes color from blue to yellow on conversion of the washing solution from an alkaline to an acidic condition.
- the color in dicator may be incorporated in any suitable manner such as by spraying it directly upon the particles at any suitable stage in the mixing operation. If the indicator is solid, it may be dissolved or dispersed in a suitable aqueous or alcoholic solution in order to form a liquid solution for ease of application to the particles.
- Other suitable dyes are phenol red, t-hymol blue, metacresol purple, etc.
- ant-caking agents such as hydra ed magnesium trisilicate, sodium carboxymethyl'cellulose, perfume, antiseptics, germicides, skin emollient materials and the like.
- EXAMPLE I Part A Sulfamic acid in the form of a powder is pretreated to apply a coating to the particles as follows: 35 parts of the sulfamic acid particles are tumbled in a Mason jar. Through an opening in the cover of the jar, a spray of a lauric acid monoethanolamide solution is introduced until 4 parts of the lauric acid monoethanolamide are deposited on the surfaces of the sulfamic acid powder.
- the spraying composition contains 30% lauric monoethanolamide dissolved in of a 1:1 mixture of Freon-l1 and Freon- 12 in a pressure resistant container.
- Part B An alkaline detergent composition is prepared in known manner by spray-drying an aqueous slurry of about 60% solids to obtain a spray-dried granular product containing 10 parts sodium dodecyl benzene sulfonate and 5 parts sodium lauryl sulfate detergents, 15 parts sodium tripolyphosphate, 4 parts sodium silicate, 5 parts sodium perborate, 6 parts moisture, and 53.7 parts sodium sulfate, with the balance of 100 parts being small amounts of perfume, fluorescent dye, and the like.
- Part A The above coated sulfamic acid particles (Part A) are tumbled with the granular alkaline detergent composition (Part B) until the product is a uniform homogeneous mixture.
- Part B the granular alkaline detergent composition
- Example III The procedure of Example I is repeated with the following formulation to obtain a uniform mixture exhibiting a neutral pH condition initially in water which is converted to an acidic pH condition subsequently:
- Example IV The procedure and formulation of Example III is repeated using 6 parts of sodium bisulfate in place of the 5 parts of sulfamic acid with similar results.
- Example V The procedure of Example I is repeated with the following ingredients to prepare a product suitable as a dry shampoo and exhibiting neutral and acidic properties successively in water:
- the following coating materials are employed in the same proportions in place of the coating agents in Examples I to VI, with equivalent results: coconut fatty acid diethanolarnide, stearic acid monoethanolamide, cetyl alcohol, stearyl alcohol, Carbowax 1500, and commercial stearic acid.
- a detergent composition which upon admixture with water is adapted to yield a non-acidic pH condition and an acidic pH condition successively to the resulting cleaning solution which comprises about /2 to 99% by weight of a water-soluble detergent selected from the group consisting of water-soluble organic neutral and alkaline anionic and non-ionic detergents, and a water-soluble acidic compound having a coating of a water-dispersible material resulting in a retarded rate of solubility, said acidic compound being present in excess so that it renders the solution acidic when dissolved, said composition dissolving sufiiciently upon admixture with water so that the resulting cleaning solution initially exhibits a non-acidic pH condition which is converted to an acidic pH condition upon dissolving of said water-soluble acidic compound after a predetermined time.
- a detergent composition in accordance with claim 1 wherein said coating is a higher fatty acid amide compound selected from the group consisting of primary amides, monoethanolamides, isopropanolamides and diethanolamidcs of fatty acids of 12 to 18 carbon atoms.
- a detergent composition in accordance with claim 1 which contains about 5 to 75% by weight of water-soluble inorganic phosphate.
- a detergent composition which upon admixture with water is adapted to yield an alkaline pH condition and an acidic pH condition successively to the resulting cleaning solution which comprises a mixture of about /2 to by weight of a water-soluble detergent selected from the group consisting of organic neutral and alkaline anionic and non-ionic detergents, at least about 5% by weight of a water-soluble alkaline inorganic salt which upon contact with water renders the solution alkaline, and a minor proportion of a water-soluble acidic ingredient which upon contact with water renders the solution acidic, said alkaline ingredient dissolving sufficiently upon admixture of said composition with water so that the resulting cleaning solution intially has an alkaline pH condition and said acidic ingredient having a coating of a water-dispersible material to retard its initial solubility but being present in a stoichiometric excess so that it subsequently converts said cleaning solution to said acidic pH condition.
- a water-soluble detergent selected from the group consisting of organic neutral and alkaline anionic and non
- a detergent composition in accordance with claim 6 which contains a color indicator to indicate by color change when the cleaning solution is converted from said alkaline to said acidic pH condition.
- a detergent composition in particulate form which upon admixture with water is adapted to yield an alkaline pH condition and an acidic pH condition successively to the resulting cleaning solution which comprises a mixture of about 5 to 50% by weight of a water-soluble detergent selected from the group consisting of organic neutral and alkaline anionic and non-ionic detergents, and the balance of total solids being primarily water-soluble inorganic salts containing at least about 5% water-soluble alkaline builder salts which upon contact with water renders it alkaline, and having admixed therewith particles of a Water-soluble normally solid acid which upon contact with Water renders it acidic, said acid having a coating of a Water-dispersible material, and said composition upon admixture with water yielding an alkaline pH condition in Water which is subsequently converted to an acidic pH condition.
- a water-soluble detergent selected from the group consisting of organic neutral and alkaline anionic and non-ionic detergents
- a detergent composition in accordance with claim 10 which contains particles of sulfamic acid coated with said material.
- a detergent composition in accordance with claim 10 which contains about /2 to 25% by weight of sodium perborate.
- a method of preparing a detergent composition which upon admixture with Water is adapted to exhibit a substantially non-acidic pH condition and an acidic pH condition to the resulting cleaning solution successively which comprises coating With a Water-dispersible compound an acidic ingredient to retard its rate of solution in water, admixing the resulting coated material with a Water-soluble detergent selected from the group consisting of the organic neutral and alkaline anionic and non-ionic detergents, and forming a homogeneous mixture.
- a method of preparing a detergent composition characterized by a mixture of Water-soluble detergent selected from the group consisting of organic neutral. and alkaline anionic and non-ionic detergents, a Water-soluble alkaline inorganic salt and a water-soluble normally solid acidic ingredient adapted to yield an alkaline pH condition and an acidic pH condition successively upon admixture with Water which comprises treating said acidic ingredient to apply a coating of a water-dispersible material, and admixing the coated acidic material with said detergent and alkaline salt to form a homogeneous mixture.
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Description
3,942,521 Tatented July 3, 1962 3,042,621 DETERGENT COMPOSITION Hans George Kirschenhauer, Allendale, N.J., assignor to Colgate-Palmolive Company, New York, N.Y., a corporation of Delaware No Drawing. Filed Nov. 1, 1957, Ser. No; 693,801 14 Claims. (Cl. 252-99) The present invention relates to an essentially nonabrasive detergent composition exhibiting substantially non-acidic and acidic pH conditions in a predetermined order of succession in water, and to a process of preparing the same, as hereinafter described and claimed.
The optimum effectiveness of detergent compositions for different functions or properties may occur at different pH ranges in water. For example, it is believed that a detergent composition exhibiting an alkaline pH in water may be preferable for various cleaning operations whereas a composition exhibiting an acidic pH may be desired for other cleaning or related operations or for conditioning of the cleaned material. It would be desirable in some instances to employ several such processing steps successively which operate initially at a pH range suitable for a particular function and then at a distinctly different pH range which is desired for a different function. Such practice could be utilized in many fields of application including commercial laundry, textile-treating and hair-treating operations and the like.
' In accordance with the present invention, it has been discovered that there can be'prepared a detergent composition exhibiting'variable and controlled pH conditions in water which comprises 'an ingredient yielding in solution an alkaline or substantially neutral pH condition, and an ingredient adapted to convert the solution to an acidic pH condition after elapse of a predetermined time. More particularly, it relates to a non-abrasive cleaning composition in particulate form which upon admixture with water is adapted to yield an alkaline or neutral pH condition and an acidic pH condition successively to the resulting cleaning solution which comprises essentially a mixture of a Water-soluble organic neutral or alkaline detergent, and a water-soluble acidic ingredient which is adapted to dissolve in' an amount sufficient to subsequently convert said cleaning solution to an acidic pH condition, said acidic ingredient having a coating of a water-dispersible material to retard its rate of solubility. A preferred embodiment comprises a particulate mixture of an organic detergent, a water-soluble alkaline builder salt and a normally solid water-soluble acid having a coating of a water-dispersible material on the acid particles. Various other preferred embodiments will be apparent in the following description. V
For convenience of illustration, the invention will be described most particularly with respect to the composition yielding successive alkaline and acidic pH conditions though it is to be understood that compositions exhibiting a different order such as successive neutral and acidic conditions are Within the scope of the invention. Where reference is made to pH conditions in the specification and claims, it is intended that such condition be illustrated by a 0.25% solution position in water. n
The composition should contain a water-soluble organic substantially neutral or alkaline detergent. Such compositions are known and are disclosed in Us. Patent of the detergent com- :No. 2,625,513, issued January .13, 1953. It is highly advantageous to incorporate an organic detergent material such as the organic anionic and non-ionic surface-active agents for a variety of effects including detergency, foaming, and surface tension and wetting effects so as tofacilitate removal of the dispersible coating on the acidic par- -to 50 alkylene oxide groups.
The soaps are generally the water-soluble salts of higher fatty acids (including rosin acids) which are derived usually from fats, oils and waxes of animal, vegetable or marine origin, e.g. tallow, coconut oil, tall oil, palm kernel oil soaps and the like. It is preferred to employ a higher alkyl aryl sulfonate such as an alkyl benzene sulfonate detergent wherein the alkyl group has about 8 to 16 carbon atoms. Suitable examples are sodium decyl benzene sulfonate, sodium dodecyl and pentadecyl sulfonates wherein the dodecyl and pentadecyl groups are derived from a propylene polymer, and sodium keryl benzene sulfonate. Other suitable agents are the surface-active sulfated or sulfonated aliphatic compounds, preferably having 8 to 22 carbon atoms. Examples thereof are sulfuric acid esters of polyhydric alcohols incompletely esterified with higher fatty acids (e.g. sodium coconut oil monoglyceride monosulfate); the long-chain pure or mixed higher alkyl sulfates (e.g. sodium lauryl sulfate and coconut fatty alcohol sulfate); the higher fatty acid ethanolamide sulfates (e.g. sodium coconut fatty acid ethanolamide sulfate); the higher fatty acid amides of amino alkyl sulfonic acids (eg sodium lauric acid amide of taurine); the higher fatty acid esters of isethionic acid; and the like. These anionic surface-active agents are used generally in the form of their water-soluble salts, such as the alkali metal (e.g. sodium, potassium), though other soluble salts such as ammonium, alkylolamine and alkaline earth metal salts may be used if desired depending upon the particular detergent.
Various non-ionic agents may be employed also, such as the non-ionic polyalkylene oxide condensates with an aliphatic or aromatic hydrophobic group. The hydrophobic organic group contains usually at least about 8 carbons condensed with at least about 5 and usually up Examples are the polyethylene oxide condensates with alkyl phenols having 6 to 20 carbons in the alkyl group such as Igepal CA and CO; the polyethylene oxide esters with higher fatty acids such as tall oil acids or lauric acid condensed with about 16 or 20 ethylene oxide groups; the polyethylene oxide condensates with higher aliphatic alcohols such as lauryl, myristyl, oleyl or stearyl alcohol with 6 to 30 moles ethylene oxide; the polyoxyethylene oxide condensates with higher fatty acid amides such as coconut fatty acid amide containing about 10 to 50 moles ethylene oxide. The water-soluble polyoxyethylene condensates With hydrophobic polyoxypropylene glycols may be employed also.
Any Water-soluble ingredient which yields an alkaline pH of above "7, preferably a pH of 8 to 12, to the aqueous solution may be employed in the composition also. The alkaline organic detergents such as the water-soluble soaps and the like described above may be employed but it is' preferred to use the water-soluble inorganic alkaline builder salts, such as the alkali metal carbonates (e.g. sodium carbonate), the alkali metal phosphates (e.g. trisodium phosphate, tetrasodium pyrophosphate, sodium tripolyphosphate), the alkali metal silicates (eg. sodium metasilicate) and the alkali metal borates (e.g. sodium borate). Any suitable base such as sodium and potassium hydroxide, and tetramethylammonium hydroxide may be employed also. Generally, it is preferred to use the normally solid organic detergent and alkaline builder salts and bases but, if desired, 'a normally'liquid mate rial may be employed by suitable combination with a Solid carrier such as by adsorption of a liquid. detergent upon a solid alkaline builder, and the like. V
The concentration of these active ingredients and mixtures thereof in the detergent compositions of the present invention vary widely according to the contemplated field of application and any amount of the detersive material may be employed which does not substantially adversely affect the desired characteristics of the product. In general, the neutral or alkaline detergent may be present in amounts from about /2 to about 99%, and preferably from about 1 to 75 by weight of total solids. With regard to detersive compositions designed primarily for comparatively light-duty cleansing purposes such as dishwashing, shampoos and the like, the composition may be free from alkaline inorganic builder salts if desired. For compositions designed for heavy-duty cleansing purposes, there is present usually at least about 5% of Water-soluble alkaline inorganic salt and about /2 to 95% detergent. A preferred formulation comprises a mixture of about 5 to 50% neutral or alkaline organic detergent with the balance of total solids being primarily water-soluble inorganic salts, preferably containing about 5 to 75% alkaline builders such as phosphates, which is admixed With a sufficient amount of an acidic ingredient as hereinafter described.
The neutral and alkaline detersive materials may be employed in the form of solid particles of any suitable size. The particle size is not critical but will vary usually from about to 400 mesh as determined on a U.S. standard sieve. The organic detergent and alkaline builder salts and the like may be in individual particulate form or they may be admixed in any suitable way to prepare mixed granules. Thus, the organic detergent and alkaline salts in the form of an aqueous slurry may be subjected to the usual drying procedures in order to obtain a relatively dry, homogeneous granular product, such as by heat-drying (e.g. drum-drying or spray-drying) of the mixture in known manner. 7
Any water-soluble acidic ingredient which will dissolve in the cleansing solution to yield an acidic pH of below 7, preferably a pH from 2 to 7, to the aqueous solution may be employed in the product. In general, it is preferred to employ a normally solid acid or acid salt in particulate form. If desired, a normally liquid material may be employed by suitable combination with a solid carrier in particulate form, such as diatomaceous earth or bentonite. The particle size of the acidic material is not critical and it may be employed in any suitable size as illustrated for the detersive materials above. Examples of suitable materials are the organic acids such as tartaric acid, maleic acid, boric acid, glutamic acid, citric acid, acetic acid, oxalic acid, gluconic acid and its lactone, and the like. Suitable inorganic acids and acid salts such as sulfamic and phosphoric acids and sodium bisulfate may be employed also.
The acidic ingredient should be used in any amount sufficient to convert the substantially neutral or alkaline solution to an acidic solution of less than 7 and preferably to a pH from about 2 to 5, when the quantity of acid has been dissolved or otherwise released in the cleansing solution. In general, it is preferred that the amount of acid be from about /2 to 50% and preferably from about 1 to by weight.
If a mixture containing alkaline and acidic ingredients in powdered form are added to water, the two materials tend to neutralize one another such that the cleansing solution will have either an alkaline or an acidic pH condition depending upon the proportion and strentgh of the different ingredients. In the case of a neutral detergent containing the acidic ingredient, the composition would yield initially an acidic condition. In order to obtain successive action of separate and distinct pH effects, it is necessary to defer or retard the rate of solubility of the acidic ingredient. This deferred acidification permits the user to utilize initially the alkaline or neutral properties of the product for optimum foaming and cleaning effects in many cases followed by use of the acidic properties of the product for other optimum effects in rinsing, dyeing, bleaching and conditioning of the cleansed material. Ac-
cordingly, the rate of solution of the acidic constituent is to be sufiiciently depressed to permit the neutral or alkaline detersive materials to dissolve first and thereby permit utilization of these properties. The acidic constituent must then be present in sufiicient amount or in stoichiometric excess over the alkaline ingredient so that when it is dissolved or released after a predetermined time the pH of the cleansing solution is reduced to the desired acidic level.
The rate of solubility of the acidic constituent may be reduced in any suitable manner. It is preferred to coat the normally solid acid particles with a solution inhibitor such as a water-dispersible coating agent. The presence of such a film or coating upon the particles of the acid will inhibit and retard the solubility of the acid when the composition is admixed with water initially. The amount of the coating is not critical and may vary from a monomolecular film to a coating of any particular size depending upon the specific coating agent, its water-dispersibility, the contemplated conditions of use, and the particular time interval which is desired before the change in the pH condition of the aqueous cleaning solution. For example, where it is contemplated to use detergent baths at relatively higher temperatures, it is desirable to employ coatings having a relatively high melting point or poor solubility in water. Thus, the predetermined time interval for the pH change may be controlled so as to be a few seconds up to any point desired in the use of the product such as up to about 30 minutes. It is preferred that the change in pH occur from about 15 seconds to 15 minutes after the product is admixed in water.
Any suitable material may be used as the coating agent such as the higher fatty alcohols, preferably having 12 to 18 carbon atoms (e.g. lauryl alcohol, coconut fatty alcohol, cetyl alcohol, stearyl alcohol), mineral oil, the higher fatty acid amide compounds, preferably having 12 to 18 carbon atoms in the acyl radical (lauric acid, coconut acid and myristic acid primary amides and the corresponding monoethanolamides, isopropanolamides and diethanolamides) and their ethylene oxide reaction products having up to about 5 moles of ethylene oxide, the higher fatty acids, preferably having 12 to 18 carbons, such as stearic acid, palmitic acid, tallow fatty acids and the like. Other coating materials are the waxlike polymers of ethylene glycol such as Oarbowax 1500, 2025 and 4000, the soluble starches and dextrins and the like. These materials may have highly limited solubility in water to extreme solubility but are effective to delay the solubility or release of the acid in the cleansing solution. The term waterdispersi ble coating agent or equivalent as used herein refers to agents of varying water solubility or dispersibility but which have been found to be dispersed or dissolve under conditions of use of the product. For example, organic materials such as lauryl alcohol and lauric acid amides and alkylol-amides have limited water solubility but in the presence of organic detergent material tend to dissolve in the cleansing solution.
The coating agent may be applied to the particles of the acid in any suitable manner. It is preferred that the coating agent be dissolved, suspended or dispersed in an appropriate solvent or heated to molten form and then sprayed or atomized on the individual acid particles to form the desired coating. Any suitable solvent may be employed, such as a normally gaseous propellant in a pressure container. Examples are the normally gaseous low-molecular weight hydrocarbon and halogenated hydrocarbon propellants, such as propane, butane, halogenated ethanes and methanes. The propellants known as the Freons and Genetrons are suitable, examples being dichlorodifluoromethane and monochlorodifluoroethane. Other solvents or dispersing mediums such as ethanol, isopropanol and aqueous alcohol mixtures may be suitably employed also. In this manner there is obtained the desired coating or film on the surface of the minor proportion usually such as from about A acid particles. Where the coating agent is normally solid it will dry to a film, and where it is normally liquid it will be adsorbed or absorbed upon the surfaces of the particles. The coating material may be applied also in solid form to the surfaces of the acid particles by mixing the coating agent in powdered form with the acid particles by suitable means for mechanical admixture including tumbling in a rotary drum. The various ingredients such as the detergent, alkaline builder salt and the coated acidic ingredient are mixed in particulate form to produce a dry, uniform granular mixture. The ingredients are admixed mechanically by tumbling, fluidizing or the like in conventional soap powder mixers known in the art or by any other suitable means for mechanical admixture.
When the final composition is added to water to form a washing solution, the organic detergent and watersoluble alkaline ingredients dissolve to form a non-acidic solution. Since the acid particles are coated with higher fatty acid amide or any other suitable coating as indicated, its rate of solution is sufficiently depressed to permit the alkaline builder to dissolve first. After a predetermined time, which may be controlled as desired by selection of the particular coating agent, the coating material disperses in the aqueous medium whereupon the acid is released and dissolves so that the pH is reduced to the desired acidic condition.
The product may contain a bleaching agent which results in effective bleaching action during use of the product. The bleaching agent may be incorporated into the product in any suitable manner, such as during or after the mixing of the essential ingredients. In general, bleaching agents are more effective in one pH condition than another. Since the product during use will form a plurality of controlled pH conditions, there can be obtained at some stage optimum conditions for a particular bleaching agent. The bleaching agent may be incorporated into the detergent composition in known manner, such as by dry mixing of the powdered materials or in any other suitable manner. If desired, the bleaching agent may be coated with any suitable material such as the coating agents previously described so that the bleaching agent is released in the same manner. Examples of suitable bleaching agents are the known oxygen and chlorine-releasing substances, such as sodium perborate, sodium, calcium and lithium hypochlorites, dichlorocyanuric acid, trichlorocyanuric acid,
Chloramine T, diohlorodimethyl hydantoin and the like.
The amount of bleaching agent is not critical but will he usually from about 0.01 to 50% of the product (e.g.
A cationic surface-active agent may be incorporated in the product also. It may be admixed in powdered or liquid form with the ingredients in any suitable manner. Vfnere it is desired to use a cationic agent, it is preferred to admix it with the acidic ingredient and coatthis mixture with the coating agent. Suitable cationic detergents are the higher alkyl quaternary ammonium compounds such as the cetyl quaternary ammonium salts. Specific examples of such materials are cetyl trimethy-l ammonium chloride, cetyl pyridinium chloride, and the like. These materials are employed in to 25% of the composition.
A suitable color indicator which would demonstrate to the consumer'whenthe change from one pH condition to the other pH condition occurs or when a particular pH level is obtained during use may be incorpoorated in the product also. The quantity of indicator is not critical except that it should be capable of producing a detectable coloration to the cleansing solution. in general, the amount of color indicator vary with the type of indicator but is usually from about 5' parts per million to 3% of the product. If methyl orange is employed, the color of the aqueous solution is yellow when the alkaline ingredient dissolves initially and the acid is coated, but the cleaning solution turns red when the acid dissolves in a stoichiometric excess after elapse of a predetermined time. Another suitable color indicator is bromo t-hymol blue which changes color from blue to yellow on conversion of the washing solution from an alkaline to an acidic condition. The color in dicator may be incorporated in any suitable manner such as by spraying it directly upon the particles at any suitable stage in the mixing operation. If the indicator is solid, it may be dissolved or dispersed in a suitable aqueous or alcoholic solution in order to form a liquid solution for ease of application to the particles. Other suitable dyes are phenol red, t-hymol blue, metacresol purple, etc.
Various known materials may he incorporated in the product also as desired. Suitable examples are minor amounts of ant-caking agents such as hydra ed magnesium trisilicate, sodium carboxymethyl'cellulose, perfume, antiseptics, germicides, skin emollient materials and the like.
The following examples are illustrative of the present invention and it will be understood that the invention is not limited thereto. All proportions indicated are by weight unless otherwise specified.
EXAMPLE I Part A Sulfamic acid in the form of a powder is pretreated to apply a coating to the particles as follows: 35 parts of the sulfamic acid particles are tumbled in a Mason jar. Through an opening in the cover of the jar, a spray of a lauric acid monoethanolamide solution is introduced until 4 parts of the lauric acid monoethanolamide are deposited on the surfaces of the sulfamic acid powder. The spraying composition contains 30% lauric monoethanolamide dissolved in of a 1:1 mixture of Freon-l1 and Freon- 12 in a pressure resistant container.
Part B An alkaline detergent composition is prepared in known manner by spray-drying an aqueous slurry of about 60% solids to obtain a spray-dried granular product containing 10 parts sodium dodecyl benzene sulfonate and 5 parts sodium lauryl sulfate detergents, 15 parts sodium tripolyphosphate, 4 parts sodium silicate, 5 parts sodium perborate, 6 parts moisture, and 53.7 parts sodium sulfate, with the balance of 100 parts being small amounts of perfume, fluorescent dye, and the like.
The above coated sulfamic acid particles (Part A) are tumbled with the granular alkaline detergent composition (Part B) until the product is a uniform homogeneous mixture. When this mixture is added to warm water in about 0.25% concentration with mild agitation, the resulting solution is alkaline initially and after a few minutes the solution is converted to an acidic pH. The final composition shows effective cleaning, laundering and bleaching properties during use of the product on soiled textiles and the like.
EXAMPLE II lowing ingredients as Parts A and B to obtain a uniform product exhibiting successively alkaline and acidic prop- 7 Part B Parts Sodium metasilicate Sodium tripolyphosphate Sodium perborate 5 Sodium dodecyl benzene sulfonate 2 Non-ionic detergent 1 Sodium sulfate 77 Ethylene oxide condensation product of polypropylene glycol with average M.W. of about 7500, ethylene oxide con tent of about 80 to 90% and M.P. of 51 to 54 C.
EXAMPLE III The procedure of Example I is repeated with the following formulation to obtain a uniform mixture exhibiting a neutral pH condition initially in water which is converted to an acidic pH condition subsequently:
Part A Parts Sulfamic acid powder 5.0 Laurie acid amide as coating agent 1.5
Part B Sodium lauryl sulfate 28.0 Sodium sulfate 71.8
Perfume 0.2
EXAMPLE IV The procedure and formulation of Example III is repeated using 6 parts of sodium bisulfate in place of the 5 parts of sulfamic acid with similar results.
EXAMPLE V The procedure of Example I is repeated with the following ingredients to prepare a product suitable as a dry shampoo and exhibiting neutral and acidic properties successively in water:
Part A Parts Boric acid powder 4.0 Cationic detergent powder 1.0 Lauric acid amide as coating agent 1.5
Part B Sodium coconut monoglyceride monosulfate 30.0 Sodium sulfate 69.6 Perfume 0.4
1 Cetyl pyridinium chloride.
EXAMPLE VI The same procedure is followed to prepare a powdered bleaching composition exhibiting successive alkaline and acidic reactions in water:
The following coating materials are employed in the same proportions in place of the coating agents in Examples I to VI, with equivalent results: coconut fatty acid diethanolarnide, stearic acid monoethanolamide, cetyl alcohol, stearyl alcohol, Carbowax 1500, and commercial stearic acid.
Although the present invention has been described with reference to particular embodiments and examples, it will be apparent to those skilled in the art that variations and 8 modifications of this invention can be made and that equivalents can be substituted therefor without departing from the principles and true spirit of the invention.
What is claimed is:
1. A detergent composition which upon admixture with water is adapted to yield a non-acidic pH condition and an acidic pH condition successively to the resulting cleaning solution which comprises about /2 to 99% by weight of a water-soluble detergent selected from the group consisting of water-soluble organic neutral and alkaline anionic and non-ionic detergents, and a water-soluble acidic compound having a coating of a water-dispersible material resulting in a retarded rate of solubility, said acidic compound being present in excess so that it renders the solution acidic when dissolved, said composition dissolving sufiiciently upon admixture with water so that the resulting cleaning solution initially exhibits a non-acidic pH condition which is converted to an acidic pH condition upon dissolving of said water-soluble acidic compound after a predetermined time.
2. A detergent composition in accordance with claim 1 wherein said acidic ingredient is a normally solid acid.
3. A detergent composition in accordance with claim 1 wherein said coating is a higher fatty acid amide compound selected from the group consisting of primary amides, monoethanolamides, isopropanolamides and diethanolamidcs of fatty acids of 12 to 18 carbon atoms.
4. A detergent composition in accordance with claim 1 which contains about 5 to 75% by weight of water-soluble inorganic phosphate.
5. A detergent composition in accordance with claim 2 wherein said acidic ingredient is sulfamic acid.
6. A detergent composition which upon admixture with water is adapted to yield an alkaline pH condition and an acidic pH condition successively to the resulting cleaning solution which comprises a mixture of about /2 to by weight of a water-soluble detergent selected from the group consisting of organic neutral and alkaline anionic and non-ionic detergents, at least about 5% by weight of a water-soluble alkaline inorganic salt which upon contact with water renders the solution alkaline, and a minor proportion of a water-soluble acidic ingredient which upon contact with water renders the solution acidic, said alkaline ingredient dissolving sufficiently upon admixture of said composition with water so that the resulting cleaning solution intially has an alkaline pH condition and said acidic ingredient having a coating of a water-dispersible material to retard its initial solubility but being present in a stoichiometric excess so that it subsequently converts said cleaning solution to said acidic pH condition.
7. A detergent composition in accordance with claim 6 wherein said acidic ingredient is a normally solid acid.
8. A detergent composition in accordance with claim 6 wherein said detergent is a water-soluble anionic organic sulfonated detergent.
9. A detergent composition in accordance with claim 6 which contains a color indicator to indicate by color change when the cleaning solution is converted from said alkaline to said acidic pH condition.
10. A detergent composition in particulate form which upon admixture with water is adapted to yield an alkaline pH condition and an acidic pH condition successively to the resulting cleaning solution which comprises a mixture of about 5 to 50% by weight of a water-soluble detergent selected from the group consisting of organic neutral and alkaline anionic and non-ionic detergents, and the balance of total solids being primarily water-soluble inorganic salts containing at least about 5% water-soluble alkaline builder salts which upon contact with water renders it alkaline, and having admixed therewith particles of a Water-soluble normally solid acid which upon contact with Water renders it acidic, said acid having a coating of a Water-dispersible material, and said composition upon admixture with water yielding an alkaline pH condition in Water which is subsequently converted to an acidic pH condition.
11. A detergent composition in accordance with claim 10 which contains particles of sulfamic acid coated with said material.
12. A detergent composition in accordance with claim 10 which contains about /2 to 25% by weight of sodium perborate.
13. A method of preparing a detergent composition which upon admixture with Water is adapted to exhibit a substantially non-acidic pH condition and an acidic pH condition to the resulting cleaning solution successively which comprises coating With a Water-dispersible compound an acidic ingredient to retard its rate of solution in water, admixing the resulting coated material with a Water-soluble detergent selected from the group consisting of the organic neutral and alkaline anionic and non-ionic detergents, and forming a homogeneous mixture.
14. A method of preparing a detergent composition characterized by a mixture of Water-soluble detergent selected from the group consisting of organic neutral. and alkaline anionic and non-ionic detergents, a Water-soluble alkaline inorganic salt and a water-soluble normally solid acidic ingredient adapted to yield an alkaline pH condition and an acidic pH condition successively upon admixture with Water which comprises treating said acidic ingredient to apply a coating of a water-dispersible material, and admixing the coated acidic material with said detergent and alkaline salt to form a homogeneous mixture.
References Cited in the file of this patent UNITED STATES PATENTS 284,464 Michaelis Sept. 4, 1883 856,672 Best et a1 June 11, 1907 871,612 Nesfield Nov. 19, 1907 980,936 Federer Jan. 10, 1911 1,075,663 Meerbott Oct. 14, 1913 1,854,235 Stoddard Apr. 19, 1932 1,966,203 Gravell July 10, 1934 1,989,765 Moss et al Feb. 5, 1935 2,196,901 Ham et al. Apr. 9, 1940 2,228,483 Raeke Jan. 14, 1941 2,308,992 Mertens Jan. 19, 1943 2,430,233 Magill Nov. 4, 1947 2,497,057 Pape et al. Feb. 7, 1950 2,498,344 Rider et a1 Feb. 21, 1950 2,540,253 Gakenheimer Feb. 6, 1951 2,578,270 Strain Dec. 11, 1951 2,763,618 Hendrix Sept. 18, 1956 FOREIGN PATENTS 749,857 Great Britain June 6, 1956
Claims (1)
1. A DETERGENT COMPOSITION WHICH UPON ADMIXTURE WITH WATER IS ADAPTED TO YIELD A NON-ACIDIC PH CONDITION AND AN ACIDIC PH CONDITION SUCCESSIVELY TO THE RESULTING CLEANING SOLUTION WHICH COMPRISES ABOUT 1/2 TO 99% BY WEIGHT OF A WATER-SOLUBLE DETERGENT SELECTED FROM THE GROUP CONSISTING OF WATER-SOLUBLE ORGANIC NEUTRAL AND ALKALINE ANIONIC AND NON-IONIC DETERGENTS, AND A WATER-SOLUBLE ACIDIC COMPOUND HAVING A COATING OF A WATER-DISPERSIBLE MATERIAL RESULTING IN A RETARDED RATE OF SOLUBILITY, SAID ACIDIC COMPOUND BEING PRESENT IN EXCESS SO THAT IT RENDERS THE SOLUTION ACIDIC WHEN DISSOLVED SAID COMPOSITION DISSOLVING SUFFICIENTLY UPON ADMIXTURE WITH WATER SO THAT THE RESULTING CLEANING SOLUTION INITIALLY EXHIBITS A NON-ACIDIC PH CONDITION WHICH IS CONVERTED TO AN ACIDIC PH CONDITION UPON DISSOLVING OF SAID WATER-SOLUBLE ACIDIC COMPOUND AFTER A PREDETERMINED TIME.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US693801A US3042621A (en) | 1957-11-01 | 1957-11-01 | Detergent composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US693801A US3042621A (en) | 1957-11-01 | 1957-11-01 | Detergent composition |
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| US3042621A true US3042621A (en) | 1962-07-03 |
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Cited By (50)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3268455A (en) * | 1961-08-23 | 1966-08-23 | Boots Pure Drug Co Ltd | Acidic denture cleaning composition |
| US3282827A (en) * | 1963-10-11 | 1966-11-01 | Norvel Company Inc | Re-refining of lubricating oils |
| US3306858A (en) * | 1965-06-17 | 1967-02-28 | Economics Lab | Process for the preparation of storage stable detergent composition |
| US3326746A (en) * | 1962-09-04 | 1967-06-20 | Lever Brothers Ltd | 1, 3-dioxane cleaning compositions |
| US3460977A (en) * | 1965-02-08 | 1969-08-12 | Minnesota Mining & Mfg | Mechanical plating |
| US3650831A (en) * | 1969-03-10 | 1972-03-21 | Armour Dial Inc | Method of cleaning surfaces |
| FR2217403A1 (en) * | 1973-02-13 | 1974-09-06 | Colgate Palmolive Co | |
| US3925234A (en) * | 1972-07-31 | 1975-12-09 | Henkel & Cie Gmbh | Coated bleach activator |
| US3926830A (en) * | 1970-11-25 | 1975-12-16 | Dainichiswika Color & Chemical | Detergent composition having polymer bonded indicator |
| US3962106A (en) * | 1974-08-01 | 1976-06-08 | Lever Brothers Company | Method for agglomerating chlorocyanurates |
| US3997459A (en) * | 1974-11-08 | 1976-12-14 | Reckitt & Colman Products Limited | Denture cleaning composition |
| US4016089A (en) * | 1974-11-11 | 1977-04-05 | Regan Glen B | Denture cleaning concentrate |
| US4079078A (en) * | 1974-06-21 | 1978-03-14 | The Procter & Gamble Company | Liquid detergent compositions |
| US4105592A (en) * | 1974-06-21 | 1978-08-08 | The Procter & Gamble Company | Liquid detergent compositions |
| US4126573A (en) * | 1976-08-27 | 1978-11-21 | The Procter & Gamble Company | Peroxyacid bleach compositions having increased solubility |
| FR2396076A1 (en) * | 1977-06-27 | 1979-01-26 | Akzo Nv | DETERGENT COMPOSITION CONTAINING AN ALKALINE CARBONATE |
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| US5635103A (en) | 1995-01-20 | 1997-06-03 | The Procter & Gamble Company | Bleaching compositions and additives comprising bleach activators having alpha-modified lactam leaving-groups |
| US5635104A (en) | 1993-06-24 | 1997-06-03 | The Procter & Gamble Company | Bleaching solutions and method utilizing selected bleach activators effective at low perhydroxyl concentrations |
| US5683724A (en) * | 1993-03-17 | 1997-11-04 | Ecolab Inc. | Automated process for inhibition of microbial growth in aqueous food transport or process streams |
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| US5879409A (en) * | 1996-02-23 | 1999-03-09 | The Procter & Gamble Company | Bleach additive and bleaching compositions having glycine anhydride activators |
| WO1999058632A1 (en) * | 1998-05-08 | 1999-11-18 | The Procter & Gamble Company | Effervescence particle |
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| US4234442A (en) * | 1978-07-14 | 1980-11-18 | Akzo N.V. | Feed unit of a detergent composition based on alkali carbonate |
| US4303542A (en) * | 1979-04-23 | 1981-12-01 | Heinlein Karl H | Powdered detergent or soak |
| US4417993A (en) * | 1979-10-30 | 1983-11-29 | Gerhard Gergely | Cleansing tablets for tooth prostheses |
| US4388077A (en) * | 1981-08-07 | 1983-06-14 | W. E. Greer Ltd. | Composition for washing fabric |
| US4725378A (en) * | 1982-03-22 | 1988-02-16 | The Dow Chemical Company | Systems for delayed release of bleaching agents |
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| US4935158A (en) * | 1986-10-30 | 1990-06-19 | Aszman Harry W | Solid detergent cleaning composition, reusable cleaning pad containing same and method of manufacture |
| US4759865A (en) * | 1986-11-06 | 1988-07-26 | Colgate-Palmolive Company | Pasty acid detergent composition |
| US4965012A (en) * | 1987-04-17 | 1990-10-23 | Olson Keith E | Water insoluble encapsulated enzymes protected against deactivation by halogen bleaches |
| US4988363A (en) * | 1987-05-06 | 1991-01-29 | Lever Brothers Company, Division Of Conopco, Inc. | Detergent bleach composition and method of cleaning fabrics |
| US4992194A (en) * | 1989-06-12 | 1991-02-12 | Lever Brothers Company, Division Of Conopco Inc. | Stably suspended organic peroxy bleach in a structured aqueous liquid |
| WO1994006573A1 (en) * | 1992-09-17 | 1994-03-31 | Deluxe Corporation | Oil based composition clean up method and composition for use therein |
| AU679693B2 (en) * | 1992-09-17 | 1997-07-10 | Deluxe Corporation | Oil based composition clean up method and composition for use therein |
| US5330769A (en) * | 1992-11-09 | 1994-07-19 | West Agro, Inc. | Acid sanitizer |
| US5409713A (en) * | 1993-03-17 | 1995-04-25 | Ecolab Inc. | Process for inhibition of microbial growth in aqueous transport streams |
| US5683724A (en) * | 1993-03-17 | 1997-11-04 | Ecolab Inc. | Automated process for inhibition of microbial growth in aqueous food transport or process streams |
| US5674538A (en) * | 1993-03-17 | 1997-10-07 | Ecolab Inc. | Process for inhibition of microbial growth in aqueous food transport or process streams |
| US6352562B1 (en) | 1993-05-20 | 2002-03-05 | The Procter & Gamble Co. | Method of cleaning fabrics using bleaching compounds comprising substituted benzoyl caprolactam bleach activators |
| US6197737B1 (en) * | 1993-05-20 | 2001-03-06 | The Procter & Gamble Company | Bleaching compounds comprising substituted benzoyl caprolactam bleach activators |
| US5635104A (en) | 1993-06-24 | 1997-06-03 | The Procter & Gamble Company | Bleaching solutions and method utilizing selected bleach activators effective at low perhydroxyl concentrations |
| US5753138A (en) * | 1993-06-24 | 1998-05-19 | The Procter & Gamble Company | Bleaching detergent compositions comprising bleach activators effective at low perhydroxyl concentrations |
| EP0651053A1 (en) * | 1993-11-03 | 1995-05-03 | The Procter & Gamble Company | Laundry detergent compositions |
| EP0651052A1 (en) * | 1993-11-03 | 1995-05-03 | The Procter & Gamble Company | Machine dishwashing detergent compositions |
| US5635103A (en) | 1995-01-20 | 1997-06-03 | The Procter & Gamble Company | Bleaching compositions and additives comprising bleach activators having alpha-modified lactam leaving-groups |
| US5797986A (en) * | 1995-02-01 | 1998-08-25 | Ecolab Inc. | Floor cleaning method |
| US5879409A (en) * | 1996-02-23 | 1999-03-09 | The Procter & Gamble Company | Bleach additive and bleaching compositions having glycine anhydride activators |
| WO1999058632A1 (en) * | 1998-05-08 | 1999-11-18 | The Procter & Gamble Company | Effervescence particle |
| US7858568B2 (en) | 2003-08-29 | 2010-12-28 | Kimberly-Clark Worldwide, Inc. | Single phase color change agents |
| US7651989B2 (en) | 2003-08-29 | 2010-01-26 | Kimberly-Clark Worldwide, Inc. | Single phase color change agents |
| US20100120644A1 (en) * | 2003-08-29 | 2010-05-13 | Kimberly-Clark Worldwide, Inc. | Single Phase Color Change Agents |
| US20050153859A1 (en) * | 2004-01-09 | 2005-07-14 | Gohl David W. | Laundry treatment composition and method and apparatus for treating laundry |
| US7682403B2 (en) * | 2004-01-09 | 2010-03-23 | Ecolab Inc. | Method for treating laundry |
| US20100170303A1 (en) * | 2004-01-09 | 2010-07-08 | Ecolab Usa Inc. | Laundry pretreatment composition and method and apparatus for treating laundry |
| US8067350B2 (en) | 2005-12-15 | 2011-11-29 | Kimberly-Clark Worldwide, Inc. | Color changing cleansing composition |
| US20080223413A1 (en) * | 2007-03-14 | 2008-09-18 | Radford Philip T | Color changing soap |
| US20180291315A1 (en) * | 2017-04-07 | 2018-10-11 | Alpha Chemical Services, Inc. | Cleaning Compositions with pH Indicators and Methods of Use |
| WO2018187683A1 (en) * | 2017-04-07 | 2018-10-11 | Alpha Chemical Services, Inc. | Cleaning compositions with ph indicators and methods of use |
| US11274270B2 (en) | 2017-04-07 | 2022-03-15 | Alpha Chemical Services, Inc. | Cleaning compositions with pH indicators and methods of use |
| US12252669B2 (en) | 2017-04-07 | 2025-03-18 | Alpha Chemical Services, Inc. | Cleaning compositions with pH indicators and methods of use |
| US10494591B2 (en) | 2017-06-22 | 2019-12-03 | Ecolab Usa Inc. | Bleaching using peroxyformic acid and an oxygen catalyst |
| US10822573B1 (en) * | 2020-02-27 | 2020-11-03 | Magnus Procurement and Logistic Solutions, Inc. | Powder descaling compositions and methods for use thereof |
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