CA2057462A1 - Detergent composition - Google Patents
Detergent compositionInfo
- Publication number
- CA2057462A1 CA2057462A1 CA002057462A CA2057462A CA2057462A1 CA 2057462 A1 CA2057462 A1 CA 2057462A1 CA 002057462 A CA002057462 A CA 002057462A CA 2057462 A CA2057462 A CA 2057462A CA 2057462 A1 CA2057462 A1 CA 2057462A1
- Authority
- CA
- Canada
- Prior art keywords
- amount
- weight
- composition according
- diol
- detergent composition
- 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.)
- Abandoned
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 75
- 239000003599 detergent Substances 0.000 title claims abstract description 26
- -1 alkyl sulphate Chemical compound 0.000 claims abstract description 27
- 239000002736 nonionic surfactant Substances 0.000 claims abstract description 12
- 229910021653 sulphate ion Inorganic materials 0.000 claims abstract description 12
- 239000004094 surface-active agent Substances 0.000 claims description 22
- 125000000217 alkyl group Chemical group 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 239000004744 fabric Substances 0.000 claims description 11
- 150000000180 1,2-diols Chemical class 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 7
- 125000003342 alkenyl group Chemical group 0.000 claims description 6
- 229920006395 saturated elastomer Polymers 0.000 claims description 5
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 4
- 150000001768 cations Chemical class 0.000 claims description 3
- 239000000344 soap Substances 0.000 claims description 3
- 230000003381 solubilizing effect Effects 0.000 claims description 3
- 125000000129 anionic group Chemical group 0.000 claims description 2
- 238000004140 cleaning Methods 0.000 claims 1
- 150000003138 primary alcohols Chemical class 0.000 claims 1
- 229930195734 saturated hydrocarbon Natural products 0.000 claims 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 claims 1
- 239000002689 soil Substances 0.000 abstract description 8
- 150000002191 fatty alcohols Chemical class 0.000 abstract 1
- 150000002009 diols Chemical class 0.000 description 21
- BAECOWNUKCLBPZ-HIUWNOOHSA-N Triolein Natural products O([C@H](OCC(=O)CCCCCCC/C=C\CCCCCCCC)COC(=O)CCCCCCC/C=C\CCCCCCCC)C(=O)CCCCCCC/C=C\CCCCCCCC BAECOWNUKCLBPZ-HIUWNOOHSA-N 0.000 description 18
- PHYFQTYBJUILEZ-UHFFFAOYSA-N Trioleoylglycerol Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC(OC(=O)CCCCCCCC=CCCCCCCCC)COC(=O)CCCCCCCC=CCCCCCCCC PHYFQTYBJUILEZ-UHFFFAOYSA-N 0.000 description 18
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 18
- 229940117972 triolein Drugs 0.000 description 18
- 229920001983 poloxamer Polymers 0.000 description 11
- 238000005406 washing Methods 0.000 description 10
- 239000000463 material Substances 0.000 description 8
- 238000010586 diagram Methods 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- 239000000460 chlorine Substances 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 6
- ZITKDVFRMRXIJQ-UHFFFAOYSA-N dodecane-1,2-diol Chemical compound CCCCCCCCCCC(O)CO ZITKDVFRMRXIJQ-UHFFFAOYSA-N 0.000 description 6
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 5
- 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 5
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 239000008103 glucose Substances 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- 229920000728 polyester Polymers 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- 230000002195 synergetic effect Effects 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-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
- 239000001768 carboxy methyl cellulose Substances 0.000 description 4
- 239000003792 electrolyte Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 3
- 235000013162 Cocos nucifera Nutrition 0.000 description 3
- 244000060011 Cocos nucifera Species 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- 239000004115 Sodium Silicate Substances 0.000 description 3
- 229910021536 Zeolite Inorganic materials 0.000 description 3
- 239000011149 active material Substances 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 239000003945 anionic surfactant Substances 0.000 description 3
- 239000007844 bleaching agent Substances 0.000 description 3
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 3
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 3
- 229940105329 carboxymethylcellulose Drugs 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
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 239000002304 perfume Substances 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- NVIFVTYDZMXWGX-UHFFFAOYSA-N sodium metaborate Chemical compound [Na+].[O-]B=O NVIFVTYDZMXWGX-UHFFFAOYSA-N 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
- 239000010457 zeolite Substances 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- 229910021532 Calcite Inorganic materials 0.000 description 2
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 2
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 2
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 2
- 229910001424 calcium ion Inorganic materials 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 229920003086 cellulose ether Polymers 0.000 description 2
- WJJMNDUMQPNECX-UHFFFAOYSA-N dipicolinic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=N1 WJJMNDUMQPNECX-UHFFFAOYSA-N 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
- 239000001923 methylcellulose Substances 0.000 description 2
- 235000010981 methylcellulose Nutrition 0.000 description 2
- 125000003703 phosphorus containing inorganic group Chemical group 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 238000001694 spray drying Methods 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- CIOXZGOUEYHNBF-UHFFFAOYSA-N (carboxymethoxy)succinic acid Chemical compound OC(=O)COC(C(O)=O)CC(O)=O CIOXZGOUEYHNBF-UHFFFAOYSA-N 0.000 description 1
- 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
- CFPOJWPDQWJEMO-UHFFFAOYSA-N 2-(1,2-dicarboxyethoxy)butanedioic acid Chemical class OC(=O)CC(C(O)=O)OC(C(O)=O)CC(O)=O CFPOJWPDQWJEMO-UHFFFAOYSA-N 0.000 description 1
- 102000013142 Amylases Human genes 0.000 description 1
- 108010065511 Amylases Proteins 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- 102000005575 Cellulases Human genes 0.000 description 1
- 108010084185 Cellulases Proteins 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-CBPJZXOFSA-N D-Gulose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@H](O)[C@H]1O WQZGKKKJIJFFOK-CBPJZXOFSA-N 0.000 description 1
- WQZGKKKJIJFFOK-WHZQZERISA-N D-aldose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-WHZQZERISA-N 0.000 description 1
- WQZGKKKJIJFFOK-IVMDWMLBSA-N D-allopyranose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@H](O)[C@@H]1O WQZGKKKJIJFFOK-IVMDWMLBSA-N 0.000 description 1
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 1
- HMFHBZSHGGEWLO-SOOFDHNKSA-N D-ribofuranose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@@H]1O HMFHBZSHGGEWLO-SOOFDHNKSA-N 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical class OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 229930091371 Fructose Natural products 0.000 description 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- 229920001479 Hydroxyethyl methyl cellulose Polymers 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- WQZGKKKJIJFFOK-VSOAQEOCSA-N L-altropyranose Chemical compound OC[C@@H]1OC(O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-VSOAQEOCSA-N 0.000 description 1
- 239000004367 Lipase Substances 0.000 description 1
- 102000004882 Lipase Human genes 0.000 description 1
- 108090001060 Lipase Proteins 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- JYXGIOKAKDAARW-UHFFFAOYSA-N N-(2-hydroxyethyl)iminodiacetic acid Chemical compound OCCN(CC(O)=O)CC(O)=O JYXGIOKAKDAARW-UHFFFAOYSA-N 0.000 description 1
- 229920001007 Nylon 4 Polymers 0.000 description 1
- 102000035195 Peptidases Human genes 0.000 description 1
- 108091005804 Peptidases Proteins 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920000388 Polyphosphate Polymers 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 239000004365 Protease Substances 0.000 description 1
- PYMYPHUHKUWMLA-LMVFSUKVSA-N Ribose Natural products OC[C@@H](O)[C@@H](O)[C@@H](O)C=O PYMYPHUHKUWMLA-LMVFSUKVSA-N 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
- 229920006243 acrylic copolymer Polymers 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
- 150000001336 alkenes Chemical group 0.000 description 1
- 125000005024 alkenyl aryl group Chemical group 0.000 description 1
- HMFHBZSHGGEWLO-UHFFFAOYSA-N alpha-D-Furanose-Ribose Natural products OCC1OC(O)C(O)C1O HMFHBZSHGGEWLO-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 description 1
- SRBFZHDQGSBBOR-STGXQOJASA-N alpha-D-lyxopyranose Chemical compound O[C@@H]1CO[C@H](O)[C@@H](O)[C@H]1O SRBFZHDQGSBBOR-STGXQOJASA-N 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 235000019418 amylase Nutrition 0.000 description 1
- 229940025131 amylases Drugs 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 238000010936 aqueous wash Methods 0.000 description 1
- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 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
- 230000009286 beneficial effect Effects 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- CMFFZBGFNICZIS-UHFFFAOYSA-N butanedioic acid;2,3-dihydroxybutanedioic acid Chemical class OC(=O)CCC(O)=O.OC(=O)CCC(O)=O.OC(=O)C(O)C(O)C(O)=O CMFFZBGFNICZIS-UHFFFAOYSA-N 0.000 description 1
- HXDRSFFFXJISME-UHFFFAOYSA-N butanedioic acid;2,3-dihydroxybutanedioic acid Chemical class OC(=O)CCC(O)=O.OC(=O)C(O)C(O)C(O)=O HXDRSFFFXJISME-UHFFFAOYSA-N 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 210000003298 dental enamel Anatomy 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
- 238000004851 dishwashing Methods 0.000 description 1
- VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 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 1
- 238000007580 dry-mixing Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229940088598 enzyme Drugs 0.000 description 1
- 238000006735 epoxidation reaction Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000007850 fluorescent dye Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 229930182830 galactose Natural products 0.000 description 1
- 230000002070 germicidal effect Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerol group Chemical group OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 159000000011 group IA salts Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 229920013821 hydroxy alkyl cellulose Polymers 0.000 description 1
- 125000005020 hydroxyalkenyl group Chemical group 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 229940071676 hydroxypropylcellulose Drugs 0.000 description 1
- 125000002951 idosyl group Chemical class C1([C@@H](O)[C@H](O)[C@@H](O)[C@H](O1)CO)* 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229910052816 inorganic phosphate Inorganic materials 0.000 description 1
- 235000019421 lipase Nutrition 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical class OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
- 150000004967 organic peroxy acids Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 150000004965 peroxy acids Chemical class 0.000 description 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920005646 polycarboxylate Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920005996 polystyrene-poly(ethylene-butylene)-polystyrene Polymers 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical class [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 229960001922 sodium perborate Drugs 0.000 description 1
- 229940045872 sodium percarbonate Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
- 239000007784 solid electrolyte Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical group OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229950009390 symclosene Drugs 0.000 description 1
- 230000008719 thickening Effects 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/83—Mixtures of non-ionic with anionic compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/825—Mixtures of compounds all of which are non-ionic
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2003—Alcohols; Phenols
- C11D3/2041—Dihydric alcohols
- C11D3/2044—Dihydric alcohols linear
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
- C11D1/146—Sulfuric acid esters
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/662—Carbohydrates or derivatives
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2003—Alcohols; Phenols
- C11D3/2006—Monohydric alcohols
- C11D3/2024—Monohydric alcohols cyclic; polycyclic
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Detergent Compositions (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
DETERGENT COMPOSITION
Detergent compositions containing primary alkyl sulphate and/or nonionic surfactant also contain alkane 1,2-diol. This leads to improved oily soil detergency when certain requirements as to proportions are complied with.
Nonionic surfactant may be ethoxylated fatty alcohol.
Alkylpolyglycoside is also possible.
DETERGENT COMPOSITION
Detergent compositions containing primary alkyl sulphate and/or nonionic surfactant also contain alkane 1,2-diol. This leads to improved oily soil detergency when certain requirements as to proportions are complied with.
Nonionic surfactant may be ethoxylated fatty alcohol.
Alkylpolyglycoside is also possible.
Description
~ ~4~
Z~57~6~
DE'rERGENT COMPOSITIONS
This invention relates to a detergent composition, S especially but not exclusively, to built compositions suitable for the washing of fabrics.
Fabric washing compositions traditionally contain one or more detergent active materials in addition to various other ingredients such as detergency builders, bleaches, fluorescers, perfumes etc. Notable applications of detergent compositions are to clean fabrics, usually by washing portable fabric items in a bowl or in a washing machine, to clean crockery and cooking utensils, again by washing in a bowl (hand dishwashing), and to clean hard surfaces such as glass, glazed surfaces, plastics, metals and enamels. A number of different detergent active materials have been proposed in the art.
We have now found that a synergistic enhancement of oily/fatty soil removal can be achieved if certain surfactants are used in certain combinations.
Accordingly, the present invention provides a built detergent composition for washing fabrics containing 2 to 50% by weight of a surfactant mixture which comprises i) a 1,2-diol of the general formula R - CH - CH2OH Z~57~6~
OH
where R is a saturated or unsaturated hydrocarbyl group containing 8 to 16 carbon atoms, ii) one or more other surfactants selected from a) primary alkyl sulphates of formula R~ OS03 M
in which R~ is z saturated, unsubstituted, branched or straight chain primary alkyl or alkenyl group containing 8 to 16 carbon atoms and M is a solubilizing cation;
b) nonionic surfactants with an HLB value of 10.5 or above, preferably 12.0 or above;
with the amounts by weight of (i), (a) and (b) such that either the amount of (b) is greater than 50% (i) and (ii) _-in which case (i) is from 5 to 40% of (i) and (ii) while (a) is not more than 25% of (i) and (ii), with the proviso that (i) is at least 10% of (i) and (ii) if (a) is from 15 to 25% of (i) and (ii);
or the amount of (b) is less than 40% of (i) and (ii) in which case (i) is at least 5% of (i) and (ii) while (a) is at least 70% of (i) and (ii) and (b) is less than 10%
of (i) and (ii) or else (i) is from 20 to 40% of (i) and (ii) while (a):(b) ranges from 40:60 to 70:30;
and with the proviso that the amount of any other non-soap anionic surfactant in the composition is less than half the 2~S7~6~
weight of said primary alkyl sulphate (a).
We have found that within these specified ranges of compositions the diol and the other surfactant(s) generally give a synergistic enhancement of oily soil removal, giving greater removal of oily soil than is found with compositions of the same surfactants which are somewhat similar but outside the specified ranges.
It should be appreciated that this enhanced detergency is an improvement relative to somewhat analogous compositions. Thus for example a composition in accordance - with the invention which is rich in primary alkyl sulphate, contains some diol and possibly a small quantity of ethoxylated alcohol may possess better oily soil detergency than either primary alkyl sulphate or the diol alone yet not-be as good as the sthoxylated alcohol alone.
Nevertheless, such a composition which is rich in primary alkyl sulphate may be preferred over the ethoxylated alcohol for other reasons, such as ability to formulate a solid product, ability to generate foam or effectiveness against other soils.
The various materials which are, or may be, included in compositions of this invention will now be considered by turn.
4 2~7~6~
It is envisaged that the hydrocarbyl group R in the general formula OH
will generally be alkyl or alkenyl of 8 to 16 carbon atoms, preferably 8 to 12. 1,2-Alkane diols are known compounds and can be prepared by standard methods for the preparation of diols. They can be manufactured from terminal olefins by epoxidation and then hydrolysis.
Other possibilities for the group R include cycloaliphatic groups and aromatic-aliphatic groups such as phenylethyl or dimethyl phenyl.
Possible primary alkyl sulphates (a), also known as sulphated fatty alcohol salts, include those of mixed alkyl chain length, in which the ratio of Cl 2 alkyl chains to C1 8 alkyl chains is in the range of from 9:4 to 1:6. A suitable material can be obtained from a mixture of synthetic lauryl and oleyl alcohols in appropriate proportions. The solubilizing cation of the alkyl sulphates is preferably an alkali metal, notably sodium or potassium.
One possibility for the nonionic surfactant (b~ is ethoxylated nonionic surfactants for which the average number of ethylene oxide residues is high enough to yield an HLB value of at least 11Ø These may in particular be ethoxylated alcohols. In such compounds the alcohol 5 Z(~7~6~
generally contains from 9 to 15 carbon atoms.
Another possibility is alkyl polyglycosides of general formula R2 o(R3 )e (G),~
provided the value of x is sufficiently high to give an HLB
of at least 11. In the general formula R2o(R3O)t(G)~
the hydrophobic group R3 is preferably aliphatic, either saturated or unsaturated, notably straight or branched alkyl, alkenyl, hydroxyalkyl or hydroxyalkenyl. However, it may include an aryl group for example alkyl-ary], alkenyl-aryl and hydroxyalkyl-aryl. Particularly preferred is that R is alkyl or alkenyl of 8 to 16 carbon atoms.
The value of t in the general formula above is _-preferably zero, so that the -(RO) t - unit of the general formula is absent. In that case the general formula becomes RO(G)~
If t is non-zero it is preferred that R3O is an ethylene oxide residue. Other likely possibilities are propylene oxide and glycerol residues. If the parameter t is non-zero so that R'O is present, the value of t (which may be an average value) will preferably lie in the range from 0.5 to 3.
The group G is typically derive~ from fructose, 6 ~7~6~
glucose, mannose, galactose, talose, gulose, allose, altrose, idose, arabinose, xylose, lyxose and/or ribose.
Preferably, the G is provided substantially exclusively by glucose units.
The value x, which is an average, is usually termed the degree of polymerization. Desirably x varies between 1 and 8. Values of x may lie between l and 3, especially 1 and 1.8.
Polyglycosides of particular interest have x in the narrow range from 1 or 1.2 up to l.4 or especially 1O3. If x exceeds 1.3 it preferably lies in the range 1.3 or 1.4 to 1.8.
When x lies in the range 1 to 1.4 it is preferred that _ R is C8 to C1 4 al~yl or alken~l.
The requirements of this invention, as stipulat20 above, signify that the surfactant mixture may be diol (i) with primary alkyl sulphate (a) diol (i) with nonionic surfactant (b) diol (i) with both of (a) and (b).
In this third case, however, the amounts of (a) and (b) must comply with certain limits which require, in qualitative terms a mixture in which (a) or (b) is preponderant over the other, or a mixture in which the amounts of (a) and (b) are not too far from being equal.
2~:~5~62 This latter possibility is a range of 40:60 to 70:30.
Mixtures of nonionic surfactants may be used. So, nonionic surfactant (b) may, for example, be an ethoxylated nonionic or an alkylpolyglycoside (each as specified above) or a mixture of the two.
Detergent compositions of the invention may contain yet further surfactants, outside the definitions specified for (i) and (ii). However, the proviso stated above, limits the amount of non-soap anionic surfactant other than primary alkyl sulphate. In general the presence of additional surfactants is not preferred, since it may harm the desired synergy. Consequently, the amount of any surfactants other than (i) and (ii) as defined is li~ely to be less than 50%
by weight better less than 25% or even 10%, of the surfactant mixture.
Additional surfactant, if present, may be anionic, nonionic or amphoteric. Cationic surfactant is possible, especially if anionic surfactant is absent but is preferably excluded.
Detergent compositions of the invention also contain detergency builder. Generally the amount of detergency builder is from 7 to 70% by weight of the composition.
If a detergent composition of this invention is in 2~57~t6~
solid form, the composition is likely to contain at least 10 or 15% of builder.
It is desirable that the compositions according to the :Lnvention be approximately neutral or preferably alkaline, that is when the composition is dissolved in an amount to give surfactant roncentration of 1 g/l in distilled water at 25C the pH should desirably be at least 7.5. For solld compositions the pH will usually be greater, such as at least 9. To achieve the required pH, the compositions may include a water-soluble alkaline salt. This salt may be a detergency builder (as described in more detail be~ow) or a non-building alkaline material.
When the compositions of the invention contain a detergency builder material, this may be any material capable of reducing the level of free calcium ions in the wash liquor and will preferably provide the compositions with other beneficial properties such as the generation of an alkaline pH and the suspension of soil removed from the fabric.
Examples of phosphorus-containing inorganic detergency builders, when present, include the water-soluble salts, especially alkali metal pyrophosphates, orthophosphates, polyphosphates and phosphonates. Specific examples of inorganic phosphate builders include sodium and potassium tripolyphosphates, orthophosphates and hexametaphosphates.
. . .
9 2~7~6~
Examples of non-phosphorus-containing inorganic detergency builders, when present, include water-soluble alkali metal carbonates, bicarbonates, silicates and crystalline and amorphous alumino silicates. Specific examples include sodium carbonate (with or without calcite seeds), potassium carbonate (with or without calcite seeds), sodium and potassium bicarbonates and silicates.
Examples of organic detergency builders, when present include the alkali metal, ammonium and substituted ammonium polyacetates, carboxylates, polycarboxylates, polyacetyl carboxylates and polyhydroxsulphonates. Specific examples include sodium, potassium, lithium, ammonium and substituted ammonium salts of ethylenediaminetetraacetic acid, nitrilotriacetic acid, oxydisuccinic acid, melitic acid, benzene polycarboxylic acids and citric acid. Further possibilities are tartrate monosuccinates, tartrate disuccinates, dipicolinic acid, cheledamic acid, carboxy methyloxysuccinate and hydroxyethyliminodiacetic acid.
Apart from the ingredients already mentioned, a number of optional ingredients may also be present. Examples of other ingredients which may be present in the composition are polymers containing carboxylic or sulphonic acid groups in acid form or wholly or partially neutralised to sodium or potassium salts, the sodium salts being preferred.
Preferred polymers are homopolymers and copolymers of Z~57~62 acrylic acid and/or maleic acid or maleic anhydride. Of especial interest are polyacrylates, polyalphahydroxyacrylates, acrylic/maleic acid copoly~ers, and acrylic phosphinates.
The molecular weights of homopolymers and copolymers are generally 1000 to 150,000, preferahly 1500 to 100,000.
The amount of any polymer may lie in the range from 0.5 to 5% by weight of the composition. Other suitable polymeric materials are cellulose ethers such as carboxy methyl cellulose, methyl cellulose, hydroxy alkyl celluloses, and mixed ethers, such as methyl hydroxy ethyl cellulose, methyl hydroxy propyl cellulose, and methyl carboxy methyl cellulose. Mixtures of different cellulose ethers, particularly mixtures of carboxy methyl cellulose and methyl cellulose, are suitable. Polyethylene glycol of molecular weight from 400 to 50,000, preferably from 1000 to 10,000, and copolymers of polyethylene oxide with polypropylene oxide are suitable as also are copolymers of polyacrylate with polyethylene glycol. Polyvinyl pyrrolidone of molecular weight of 10,000 to 60,000 preferably of 30,000 to 50,000 and copolymers of polyvinyl pyrrolidone with other poly pyrrolidones are suitable. Polyacrylic phosphinates and related copolymers of molecular weight 1000 to 100,000, in particular 3000 to 30,000 are also suitable.
Further examples of other ingredients which may be present in the composition include fabric softening agents Zl?57~6~:
such as fatty amines, fabric softening clay materials, lather boosters such as alkanolamides, particularly the monoethanolamides derived from palm kernel ~atty acids and coconut fatty acids, lather depressants, oxygen-releasing bleaching agents such as sodium perborate and sodium percarbonate, typically accompanied by peracid bleach precursors, organic peracids, chlorine-releasing bleaching agents such as trichloroisocyanuric acid, inorganic salts such as sodium sulphate, and, usually present in very minor amounts, fluorescent agents, perfumes including deodorant perfumes, enzymes such as cellulases, proteases, lipases and amylases, germicides and colourants.
The detergent compositions according to the invention may be in any suitable form including powders, bars, liquids and pastes. For example suitable liquid compositions may be non-aqueous or aqueous, the latter being either isotropic or lamellar structured. The compositions may be prepared by a number of different methods according to their physical form. In the case of granular products they may be prepared by dry-mixing, coagglomeration, spray-drying from an agueous slurry or any combination of these methods.
One preferred physical form is a granule incorporating a detergency builder salt. This may be prepared by conventional granulation techniques or spray drying.
Another preferred physical form is a lamellar 2C~7'~6~
structured aqueous liquid, for heavy duty fabrics washing, in which the surfactant mixture provides structure capable of suspending particulate solids. For such forms in particular the surfactant (ii) may be nonionic surfactant (b). The aqueous continuous phase of such a liquid will usually contain dissolved electrolyte. Electrolyte may be dissolved only in the aqueous continuous phase or may also be present as suspended solid particles. Particles of solid materials which are insoluble in the aqueous phase may be suspended alternatively or in addition to any solid electrolyte particles.
Three common product forms which are liquid are liquids for heavy duty fabrics washing, liquid abraslve cleaners and general purpose cleaners. In the first class, the suspended solid can comprise suspended solids which are -.
substantially the same as the dissolved electrolyte, being an excess of same beyond the solubility limit. This solid is usually present as a detergency builder, i.e. to counteract the effects of calcium ion water hardness in the wash. In the second class, the suspended solid usually comprises a particulate abrasive, insoluble in the system.
In that case the electrolyte, present to contribute to the structuring of the active material in the dispersed phase, is generally different from the abrasive compounds. In certain cases, the abrasive can however comprise partially soluble salts which dissolve when the product is diluted.
In the third class, the structure is usually used for Z~57/~6~
thickening the product to give consumer-preferred flow properties, and sometimes to suspend pigment particles.
In the following examples the parts and percentages are by weight. Figures 1 and 2 are triangular plots of results from Examples 3 and 7.
Example 1 Compositions were prepared having as a general formulation:
% by weight Detergent active 13 Zeolite 24 Sodium silicate 0.8 Sokolan CP5 4 Sodium carbonate (anhydrous) 12 Sodium carboxymethyl cellulose 0.5 Sodium metaborate 11 Water balance to lO0~
Sokolan CP5 is an acrylic/maleic copolymer available from BASF.
The detergent active was provided by various proportions of Dodecane 1,2-diol available from Aldrich Chemical Co. and Synperonic A7 available from I.C.I.
Synperonic A7 is a C1 3 -Cl 5 alcohol ethoxylated with an average of seven ethylene oxide residues. It has an HLB of 11.7.
, :
2~57~62 The compositions were added to 24FH water at a concentration of 6g/litre. The resulting wash liquors had a p~ of 10 and were used to wash polyester test cloths soil~d with radiolabelled triolein. Washing was carried out at 40C for 20 minutes in a Tergotometer.
The removal of radiolabelled triolein was deter~ined and the results were:
Ratio ~ Triolein removal Synperonic A7 : 1,2-diol 100:0 68.9 85:15 74,5 69:31 62.7 54:36 13.7 Example 2 Compositions were prepared having as a general formulation:
~ by weight Detergent active 13 Zeolite 24 Sodium silicate 0.8 Sokolan CP5 4 Sodium carbonate (anhydrous) 10 Sodium sulphate 20 Sodium metaborate 11 Water balance to 100%
2~57'~2 The detergent active was provided by mixtures of various 1,2-diols and primary alkyl sulphate ~PAS) with an alkyl chain length of 14 and 15 carbon atoms. The alkane 1,2-diols ranged from C~ to C1 6 chain length.
The compositions were added to 24FH water at a concentration of 6g/litre giving wash liquors with a pH of 10. These were used to wash polyester test cloths soiled with radiolabelled triolein, as in the preceding example.
Results were as follows:
Ratio PAS:DIOL ~ Triolein Removal ~ DIOLC10 DIOL C1 2 DIOL C~ 4 DIOL Cl 6 DIOL
100:0 34.g38.4 38.4 38.4 38.4 95:5 - - - - 41.9 90:10 - 36.7 41.5 44.5 42.4 85:15 - - - - 42.9 80:20 33.5 43.0 46.9 46.2 70:30 27.5 - - 37.7 37.6 60:40 27.4 45.0 23.3 -- 1 1 . 9 40:60 - 26.6 7.3 5.4 8.6 30:70 19.3 20:80 - - - 2~2 0:100 1.1 0.56 - 1.1 2.7 .
'. ': ' ' : ' "
.
., 16 2 ~ ~7 ~62 Rxample 3 The procedure of Example 2 was repeated using as detergent active various mixtures of Cl 2 1, 2-diol, primary alkyl sulphate with a chain length of 14 and 15 carbon atoms and Synperonic A7 as used in Example 1. The results (%
triolein removal) are given in a table below. In this table the amounts of the individual surfactants are given as percentages of the total quantity of all three surfactants, which was 13% of the composition.
PASSynperonic A7 C1 2 1~ 2-Diol % Triolein Removal 0 lO0 0 56.8 15.4 84.6 0 25.5 30.8 69.2 0 11.4 1546.2 53.8 0 9.0 69.2 30.8 0 9.3 92.3 7.7 0 22.2 100 0 0 23.0 0 84.6 15.4 63.0 2015.4 69.2 15.4 ~1.4 30.8 53.8 15.4 36.9 38.5 46.1 15.4 26.5 42.3 42.3 15.4 27.8 41.1 38.5 15.4 33.7 2553.8 30.8 15.4 32.9 61.5 23.1 15.4 26.8 69.2 15.4 15.4 15.6 76.9 7.7 15.4 39.9 .
17 2 ~ ~7~6~
84.6 0 15.4 39.3 61.5 15.4 23.1 29.3 0 69.2 30.8 55.2 15.4 53.8 30.8 40.7 23.1 46.1 30.8 31.4 30.8 38.4 30.8 36.5 46.1 23.1 30.8 34.1 53.8 15.4 30.8 20.2 61.5 7.7 30.8 21.9 69.2 0 30.8 28.9 0 53.9 46.1 15.8 15.4 38.5 46.1 23.5 30.8 23.1 46.1 28.0 46.1 7.8 46.1 30.2 53.9 0 46.1 7.6 0 46.2 53.8 3.7 30.8 15.4 53.8 2.3 38.5 7.7 53.8 11.6 30.8 7.7 61.5 6.0 38.5 0 61.5 5.8 0 30.8 69.2 1.9 These results are also plotted on a triangular diagram whlch appears as Fig. 1.
As can be seen from this diagram's right-hand corner, there is synergistic enhancement of detergency with mixtures containing diol and PAS only. The maximum occurs at around ' ' ' .
, Z~57/~6~
a 4:1 ratio of diol : PAS. If a limited amount of Synperonic A7 is introduced into such a mixture, the synergistic enhancement is still observed, but if the amount of Synperonic A7 is more than about 10% of the three surfactants, or the amount of PAS is less than 70% the mixtures are outside the scope of the invention and give relatively poorer triolein removal.
Analogously, there is a synergistic enhancement of detergency for mixtures containing diol and Synperonic only.
This is at the left-hand edge of the triangular diagram. If PAS is incorporated into such mixtures, detergency deteriorates. The requirements of this invention as stated originally circumscribe the area in which triolein removal is good.
. .
Roughly in the centre of the diagram is an area of improved detergency, falling within the scope of this invention. However it gives slightly less triolein removal than the areas at the left and right sides of the diagram which may therefore be preferred.
Example 4 Aqueous wash liquors were prepared containing the following materials in deionized water.
2C'57~62 Alkyl polyglycoside }
} one gram pe.r litre Dodecane 1,2-diol }
Sodium metaborate 0.05 molar These quantities would be typical of using 6g/litre of a detergent product containing 16~7% by weight surfactant.
The wash liquors had a pH of about lO resulting from the presence of the metaborate.
The alkylpolyglycoside was APG 300 from Horizon Chemical Co. This was of the formula Ro(G)x where R is a 9 to 11 carbon alkyl chain, G is glucose and x has an averaye value of 1.4. It had an HLB value of approximately 11 to 12. The dodecane 1,2-diol is available from Aldrich Chemical Co.
Wash liquors were prepared with various ratios of the two surfactants and used to wash polyester test cloths soiled with radiolabelled triolein. Washing was carried out at 40C for 20 minutes in a Tergotometer.
The removal of triolein was determined and the results were:
Z~57~6~
Ratio% Trio~ein removal APG 300/1,2-diol 100/0 58.9 95/5 60.2 90/10 58.5 80/20 41.2 60/40 4.5 40/60 2.2 20/80 1.7 0/100 1.7 Example 5 Example 4 was repeated using a different alkylpolyglycoside. APG 500 from Horizon was used. This has the formula Ro(G)x where R is Cl 2 and Cl 3 alkyl, G is glucose and x is 1.4. It had an HLB value of approximately 11.5 to 12.5.
Results were:
20 Ratio% Triolein removal APG 500:1,2-diol 100:0 45.3 90:10 54.1 80:20 37.1 60:40 6.2 40:60 2.3 20:80 1.8 0:100 1.7 21 2~57~62 Example 6 The procedure of Example 1 was repeated using as detergent active various proportions of an alkylpolyglycoside and Dodecane 1,2-diol. The alkylpolyglycoside was APG 550 from Horizon. This is of the general formula Ro(G)x where R is a 12 and 13 carbon atom alkyl chain, G is glucose and x has an average value of 1.8. It had an HLB value of approximately 12 to 13.
The compositions were added to 24FH water at a concentration of 6g/litre. The resulting wash liquors had a pH of 10 and were used to wash polyester test cloths as in previous Examples. The cloths came from a different batch, conseguently these figures cannot be compared directly with the results from Example 1.
Results were:
Ratio% Triolein removal APG 550:1,2-diol 100:0 43.5 92:8 58.0 85:15 32.2 69:31 5.9 54:46 2.6 22 ZC~57~62 Example 7 The previous Example 6 was repeated, using various m:ixtures of Synperonic A7 and APG 550 as the nonionic surfactant. The results, including these of the previous Example are given in the following table in which the amounts of APG 550, Dodecane 1,2-diol and Synperonic A7 are expressed as percentages of the total quantity of all three (which was a constant 13% of the overall composition). The results are also plotted as a triangular diagram which appears as Fig. 2.
2C'S~L6~
APG 550 Synperonic A7 C1 2 1,2 Diol~ Triolein Removal 0 100 0 68.9 15.4 84.6 0 66.9 30.8 69.2 0 64.2 50.0 50.0 0 62.5 69.2 30.8 ~ 57.~
100 0 0 43.5 80.8 11.5 7.7 63.3 92.3 0 7.7 58.0 0 84.6 15.4 74.5 23.1 61.5 15.4 68.0 53.8 30.8 15.4 63.8 69.2 15.4 15.4 58.5 84.6 0 15.4 32.2 0 69.2 30.8 62.7 15.4 53.8 30.8 59.2 23.1 46.1 30.8 55.0 38.4 30.8 30.8 47.8 69.2 0 30.8 5.9 0 53.8 46.2 13.6 23.1 30.8 46.2 11.3 38.4 15.4 46.2 8.7 53.8 0 46.2 2.6 It can be seen from this triangular diagram that for all proportions of APG 550: Synperonic A7, there iS a mixture with diol which gives greater triolein removal than without the diol.
2C~S7~6~
Example 8 Compositions were prepared having as a general formulation:
~ by weight Detergent active 17 Zeolite 32 Sodium silicate 0.8 Sokolan CP5 4.0 10 Sodium carbonate (anhydrous) 14.5 Sodium metaborate 16.5 The detergent active was provided by various proportions of alkylpolyglycoside, and dodecane 1,2-diol and coconut alkyl sulphate (PAS). The alkylpolyglycoside was APG 600 from Horizon (also available as Plantaren APG 600 from Henkel). This is of the general formula Ro(G)x where R is a coconut alkyl chain (i.e. principally C1 2 and Cl4), G is glucose and x has an average value of 1.4. It has an HLB value of approximately 12.
The compositions were added to 24 FH water at a concentration of 5 g/litre and used to wash polyester test cloths by the procedure as in Examples 1 and 2.
25Z~S7~62 Results were:
Ratio % Triolein removal PAS : APG 600 : 1,2-diol 0.0 100.0 0.0 60.3 25.0 75.0 000 49.2 50.0 50.00 0.0 50.1 75.0 25.0 0.0 46.5 100.0 0.0 0.0 53.8 0,O 93,0 7.0 66.7 109.3 83.7 7.0 59.1 93.0 0.0 7,0 61.0 0.0 86.0 14.0 70.0 , 17.2 68.8 14.0 63.3 51.6 34.4 14.0 58.7 1568.8 17.2 14.0 54.7 86.0 0.0 1~.0 58.0 0.0 79.0 21.0 64.1 15.8 63.2 21.0 63.6 39.5 39.5 21.0 61.2 2051.7 27.3 21.0 55.1 79,0 0.0 21.0 52.0 ; 45.5 19.5 35.0 45.4 29.0 29.0 42.0 27.1 0.0 51.0 49.0 7.8 2551.0 0.0 49.0 13.9 0.0 30.0 70.0 1.7 30.0 0.0 70.0 3.0 , 26 2~57~6~:
Again it can be seen that incorporation of diol in limited amounts leads to improved triolein removal.
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DE'rERGENT COMPOSITIONS
This invention relates to a detergent composition, S especially but not exclusively, to built compositions suitable for the washing of fabrics.
Fabric washing compositions traditionally contain one or more detergent active materials in addition to various other ingredients such as detergency builders, bleaches, fluorescers, perfumes etc. Notable applications of detergent compositions are to clean fabrics, usually by washing portable fabric items in a bowl or in a washing machine, to clean crockery and cooking utensils, again by washing in a bowl (hand dishwashing), and to clean hard surfaces such as glass, glazed surfaces, plastics, metals and enamels. A number of different detergent active materials have been proposed in the art.
We have now found that a synergistic enhancement of oily/fatty soil removal can be achieved if certain surfactants are used in certain combinations.
Accordingly, the present invention provides a built detergent composition for washing fabrics containing 2 to 50% by weight of a surfactant mixture which comprises i) a 1,2-diol of the general formula R - CH - CH2OH Z~57~6~
OH
where R is a saturated or unsaturated hydrocarbyl group containing 8 to 16 carbon atoms, ii) one or more other surfactants selected from a) primary alkyl sulphates of formula R~ OS03 M
in which R~ is z saturated, unsubstituted, branched or straight chain primary alkyl or alkenyl group containing 8 to 16 carbon atoms and M is a solubilizing cation;
b) nonionic surfactants with an HLB value of 10.5 or above, preferably 12.0 or above;
with the amounts by weight of (i), (a) and (b) such that either the amount of (b) is greater than 50% (i) and (ii) _-in which case (i) is from 5 to 40% of (i) and (ii) while (a) is not more than 25% of (i) and (ii), with the proviso that (i) is at least 10% of (i) and (ii) if (a) is from 15 to 25% of (i) and (ii);
or the amount of (b) is less than 40% of (i) and (ii) in which case (i) is at least 5% of (i) and (ii) while (a) is at least 70% of (i) and (ii) and (b) is less than 10%
of (i) and (ii) or else (i) is from 20 to 40% of (i) and (ii) while (a):(b) ranges from 40:60 to 70:30;
and with the proviso that the amount of any other non-soap anionic surfactant in the composition is less than half the 2~S7~6~
weight of said primary alkyl sulphate (a).
We have found that within these specified ranges of compositions the diol and the other surfactant(s) generally give a synergistic enhancement of oily soil removal, giving greater removal of oily soil than is found with compositions of the same surfactants which are somewhat similar but outside the specified ranges.
It should be appreciated that this enhanced detergency is an improvement relative to somewhat analogous compositions. Thus for example a composition in accordance - with the invention which is rich in primary alkyl sulphate, contains some diol and possibly a small quantity of ethoxylated alcohol may possess better oily soil detergency than either primary alkyl sulphate or the diol alone yet not-be as good as the sthoxylated alcohol alone.
Nevertheless, such a composition which is rich in primary alkyl sulphate may be preferred over the ethoxylated alcohol for other reasons, such as ability to formulate a solid product, ability to generate foam or effectiveness against other soils.
The various materials which are, or may be, included in compositions of this invention will now be considered by turn.
4 2~7~6~
It is envisaged that the hydrocarbyl group R in the general formula OH
will generally be alkyl or alkenyl of 8 to 16 carbon atoms, preferably 8 to 12. 1,2-Alkane diols are known compounds and can be prepared by standard methods for the preparation of diols. They can be manufactured from terminal olefins by epoxidation and then hydrolysis.
Other possibilities for the group R include cycloaliphatic groups and aromatic-aliphatic groups such as phenylethyl or dimethyl phenyl.
Possible primary alkyl sulphates (a), also known as sulphated fatty alcohol salts, include those of mixed alkyl chain length, in which the ratio of Cl 2 alkyl chains to C1 8 alkyl chains is in the range of from 9:4 to 1:6. A suitable material can be obtained from a mixture of synthetic lauryl and oleyl alcohols in appropriate proportions. The solubilizing cation of the alkyl sulphates is preferably an alkali metal, notably sodium or potassium.
One possibility for the nonionic surfactant (b~ is ethoxylated nonionic surfactants for which the average number of ethylene oxide residues is high enough to yield an HLB value of at least 11Ø These may in particular be ethoxylated alcohols. In such compounds the alcohol 5 Z(~7~6~
generally contains from 9 to 15 carbon atoms.
Another possibility is alkyl polyglycosides of general formula R2 o(R3 )e (G),~
provided the value of x is sufficiently high to give an HLB
of at least 11. In the general formula R2o(R3O)t(G)~
the hydrophobic group R3 is preferably aliphatic, either saturated or unsaturated, notably straight or branched alkyl, alkenyl, hydroxyalkyl or hydroxyalkenyl. However, it may include an aryl group for example alkyl-ary], alkenyl-aryl and hydroxyalkyl-aryl. Particularly preferred is that R is alkyl or alkenyl of 8 to 16 carbon atoms.
The value of t in the general formula above is _-preferably zero, so that the -(RO) t - unit of the general formula is absent. In that case the general formula becomes RO(G)~
If t is non-zero it is preferred that R3O is an ethylene oxide residue. Other likely possibilities are propylene oxide and glycerol residues. If the parameter t is non-zero so that R'O is present, the value of t (which may be an average value) will preferably lie in the range from 0.5 to 3.
The group G is typically derive~ from fructose, 6 ~7~6~
glucose, mannose, galactose, talose, gulose, allose, altrose, idose, arabinose, xylose, lyxose and/or ribose.
Preferably, the G is provided substantially exclusively by glucose units.
The value x, which is an average, is usually termed the degree of polymerization. Desirably x varies between 1 and 8. Values of x may lie between l and 3, especially 1 and 1.8.
Polyglycosides of particular interest have x in the narrow range from 1 or 1.2 up to l.4 or especially 1O3. If x exceeds 1.3 it preferably lies in the range 1.3 or 1.4 to 1.8.
When x lies in the range 1 to 1.4 it is preferred that _ R is C8 to C1 4 al~yl or alken~l.
The requirements of this invention, as stipulat20 above, signify that the surfactant mixture may be diol (i) with primary alkyl sulphate (a) diol (i) with nonionic surfactant (b) diol (i) with both of (a) and (b).
In this third case, however, the amounts of (a) and (b) must comply with certain limits which require, in qualitative terms a mixture in which (a) or (b) is preponderant over the other, or a mixture in which the amounts of (a) and (b) are not too far from being equal.
2~:~5~62 This latter possibility is a range of 40:60 to 70:30.
Mixtures of nonionic surfactants may be used. So, nonionic surfactant (b) may, for example, be an ethoxylated nonionic or an alkylpolyglycoside (each as specified above) or a mixture of the two.
Detergent compositions of the invention may contain yet further surfactants, outside the definitions specified for (i) and (ii). However, the proviso stated above, limits the amount of non-soap anionic surfactant other than primary alkyl sulphate. In general the presence of additional surfactants is not preferred, since it may harm the desired synergy. Consequently, the amount of any surfactants other than (i) and (ii) as defined is li~ely to be less than 50%
by weight better less than 25% or even 10%, of the surfactant mixture.
Additional surfactant, if present, may be anionic, nonionic or amphoteric. Cationic surfactant is possible, especially if anionic surfactant is absent but is preferably excluded.
Detergent compositions of the invention also contain detergency builder. Generally the amount of detergency builder is from 7 to 70% by weight of the composition.
If a detergent composition of this invention is in 2~57~t6~
solid form, the composition is likely to contain at least 10 or 15% of builder.
It is desirable that the compositions according to the :Lnvention be approximately neutral or preferably alkaline, that is when the composition is dissolved in an amount to give surfactant roncentration of 1 g/l in distilled water at 25C the pH should desirably be at least 7.5. For solld compositions the pH will usually be greater, such as at least 9. To achieve the required pH, the compositions may include a water-soluble alkaline salt. This salt may be a detergency builder (as described in more detail be~ow) or a non-building alkaline material.
When the compositions of the invention contain a detergency builder material, this may be any material capable of reducing the level of free calcium ions in the wash liquor and will preferably provide the compositions with other beneficial properties such as the generation of an alkaline pH and the suspension of soil removed from the fabric.
Examples of phosphorus-containing inorganic detergency builders, when present, include the water-soluble salts, especially alkali metal pyrophosphates, orthophosphates, polyphosphates and phosphonates. Specific examples of inorganic phosphate builders include sodium and potassium tripolyphosphates, orthophosphates and hexametaphosphates.
. . .
9 2~7~6~
Examples of non-phosphorus-containing inorganic detergency builders, when present, include water-soluble alkali metal carbonates, bicarbonates, silicates and crystalline and amorphous alumino silicates. Specific examples include sodium carbonate (with or without calcite seeds), potassium carbonate (with or without calcite seeds), sodium and potassium bicarbonates and silicates.
Examples of organic detergency builders, when present include the alkali metal, ammonium and substituted ammonium polyacetates, carboxylates, polycarboxylates, polyacetyl carboxylates and polyhydroxsulphonates. Specific examples include sodium, potassium, lithium, ammonium and substituted ammonium salts of ethylenediaminetetraacetic acid, nitrilotriacetic acid, oxydisuccinic acid, melitic acid, benzene polycarboxylic acids and citric acid. Further possibilities are tartrate monosuccinates, tartrate disuccinates, dipicolinic acid, cheledamic acid, carboxy methyloxysuccinate and hydroxyethyliminodiacetic acid.
Apart from the ingredients already mentioned, a number of optional ingredients may also be present. Examples of other ingredients which may be present in the composition are polymers containing carboxylic or sulphonic acid groups in acid form or wholly or partially neutralised to sodium or potassium salts, the sodium salts being preferred.
Preferred polymers are homopolymers and copolymers of Z~57~62 acrylic acid and/or maleic acid or maleic anhydride. Of especial interest are polyacrylates, polyalphahydroxyacrylates, acrylic/maleic acid copoly~ers, and acrylic phosphinates.
The molecular weights of homopolymers and copolymers are generally 1000 to 150,000, preferahly 1500 to 100,000.
The amount of any polymer may lie in the range from 0.5 to 5% by weight of the composition. Other suitable polymeric materials are cellulose ethers such as carboxy methyl cellulose, methyl cellulose, hydroxy alkyl celluloses, and mixed ethers, such as methyl hydroxy ethyl cellulose, methyl hydroxy propyl cellulose, and methyl carboxy methyl cellulose. Mixtures of different cellulose ethers, particularly mixtures of carboxy methyl cellulose and methyl cellulose, are suitable. Polyethylene glycol of molecular weight from 400 to 50,000, preferably from 1000 to 10,000, and copolymers of polyethylene oxide with polypropylene oxide are suitable as also are copolymers of polyacrylate with polyethylene glycol. Polyvinyl pyrrolidone of molecular weight of 10,000 to 60,000 preferably of 30,000 to 50,000 and copolymers of polyvinyl pyrrolidone with other poly pyrrolidones are suitable. Polyacrylic phosphinates and related copolymers of molecular weight 1000 to 100,000, in particular 3000 to 30,000 are also suitable.
Further examples of other ingredients which may be present in the composition include fabric softening agents Zl?57~6~:
such as fatty amines, fabric softening clay materials, lather boosters such as alkanolamides, particularly the monoethanolamides derived from palm kernel ~atty acids and coconut fatty acids, lather depressants, oxygen-releasing bleaching agents such as sodium perborate and sodium percarbonate, typically accompanied by peracid bleach precursors, organic peracids, chlorine-releasing bleaching agents such as trichloroisocyanuric acid, inorganic salts such as sodium sulphate, and, usually present in very minor amounts, fluorescent agents, perfumes including deodorant perfumes, enzymes such as cellulases, proteases, lipases and amylases, germicides and colourants.
The detergent compositions according to the invention may be in any suitable form including powders, bars, liquids and pastes. For example suitable liquid compositions may be non-aqueous or aqueous, the latter being either isotropic or lamellar structured. The compositions may be prepared by a number of different methods according to their physical form. In the case of granular products they may be prepared by dry-mixing, coagglomeration, spray-drying from an agueous slurry or any combination of these methods.
One preferred physical form is a granule incorporating a detergency builder salt. This may be prepared by conventional granulation techniques or spray drying.
Another preferred physical form is a lamellar 2C~7'~6~
structured aqueous liquid, for heavy duty fabrics washing, in which the surfactant mixture provides structure capable of suspending particulate solids. For such forms in particular the surfactant (ii) may be nonionic surfactant (b). The aqueous continuous phase of such a liquid will usually contain dissolved electrolyte. Electrolyte may be dissolved only in the aqueous continuous phase or may also be present as suspended solid particles. Particles of solid materials which are insoluble in the aqueous phase may be suspended alternatively or in addition to any solid electrolyte particles.
Three common product forms which are liquid are liquids for heavy duty fabrics washing, liquid abraslve cleaners and general purpose cleaners. In the first class, the suspended solid can comprise suspended solids which are -.
substantially the same as the dissolved electrolyte, being an excess of same beyond the solubility limit. This solid is usually present as a detergency builder, i.e. to counteract the effects of calcium ion water hardness in the wash. In the second class, the suspended solid usually comprises a particulate abrasive, insoluble in the system.
In that case the electrolyte, present to contribute to the structuring of the active material in the dispersed phase, is generally different from the abrasive compounds. In certain cases, the abrasive can however comprise partially soluble salts which dissolve when the product is diluted.
In the third class, the structure is usually used for Z~57/~6~
thickening the product to give consumer-preferred flow properties, and sometimes to suspend pigment particles.
In the following examples the parts and percentages are by weight. Figures 1 and 2 are triangular plots of results from Examples 3 and 7.
Example 1 Compositions were prepared having as a general formulation:
% by weight Detergent active 13 Zeolite 24 Sodium silicate 0.8 Sokolan CP5 4 Sodium carbonate (anhydrous) 12 Sodium carboxymethyl cellulose 0.5 Sodium metaborate 11 Water balance to lO0~
Sokolan CP5 is an acrylic/maleic copolymer available from BASF.
The detergent active was provided by various proportions of Dodecane 1,2-diol available from Aldrich Chemical Co. and Synperonic A7 available from I.C.I.
Synperonic A7 is a C1 3 -Cl 5 alcohol ethoxylated with an average of seven ethylene oxide residues. It has an HLB of 11.7.
, :
2~57~62 The compositions were added to 24FH water at a concentration of 6g/litre. The resulting wash liquors had a p~ of 10 and were used to wash polyester test cloths soil~d with radiolabelled triolein. Washing was carried out at 40C for 20 minutes in a Tergotometer.
The removal of radiolabelled triolein was deter~ined and the results were:
Ratio ~ Triolein removal Synperonic A7 : 1,2-diol 100:0 68.9 85:15 74,5 69:31 62.7 54:36 13.7 Example 2 Compositions were prepared having as a general formulation:
~ by weight Detergent active 13 Zeolite 24 Sodium silicate 0.8 Sokolan CP5 4 Sodium carbonate (anhydrous) 10 Sodium sulphate 20 Sodium metaborate 11 Water balance to 100%
2~57'~2 The detergent active was provided by mixtures of various 1,2-diols and primary alkyl sulphate ~PAS) with an alkyl chain length of 14 and 15 carbon atoms. The alkane 1,2-diols ranged from C~ to C1 6 chain length.
The compositions were added to 24FH water at a concentration of 6g/litre giving wash liquors with a pH of 10. These were used to wash polyester test cloths soiled with radiolabelled triolein, as in the preceding example.
Results were as follows:
Ratio PAS:DIOL ~ Triolein Removal ~ DIOLC10 DIOL C1 2 DIOL C~ 4 DIOL Cl 6 DIOL
100:0 34.g38.4 38.4 38.4 38.4 95:5 - - - - 41.9 90:10 - 36.7 41.5 44.5 42.4 85:15 - - - - 42.9 80:20 33.5 43.0 46.9 46.2 70:30 27.5 - - 37.7 37.6 60:40 27.4 45.0 23.3 -- 1 1 . 9 40:60 - 26.6 7.3 5.4 8.6 30:70 19.3 20:80 - - - 2~2 0:100 1.1 0.56 - 1.1 2.7 .
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.
., 16 2 ~ ~7 ~62 Rxample 3 The procedure of Example 2 was repeated using as detergent active various mixtures of Cl 2 1, 2-diol, primary alkyl sulphate with a chain length of 14 and 15 carbon atoms and Synperonic A7 as used in Example 1. The results (%
triolein removal) are given in a table below. In this table the amounts of the individual surfactants are given as percentages of the total quantity of all three surfactants, which was 13% of the composition.
PASSynperonic A7 C1 2 1~ 2-Diol % Triolein Removal 0 lO0 0 56.8 15.4 84.6 0 25.5 30.8 69.2 0 11.4 1546.2 53.8 0 9.0 69.2 30.8 0 9.3 92.3 7.7 0 22.2 100 0 0 23.0 0 84.6 15.4 63.0 2015.4 69.2 15.4 ~1.4 30.8 53.8 15.4 36.9 38.5 46.1 15.4 26.5 42.3 42.3 15.4 27.8 41.1 38.5 15.4 33.7 2553.8 30.8 15.4 32.9 61.5 23.1 15.4 26.8 69.2 15.4 15.4 15.6 76.9 7.7 15.4 39.9 .
17 2 ~ ~7~6~
84.6 0 15.4 39.3 61.5 15.4 23.1 29.3 0 69.2 30.8 55.2 15.4 53.8 30.8 40.7 23.1 46.1 30.8 31.4 30.8 38.4 30.8 36.5 46.1 23.1 30.8 34.1 53.8 15.4 30.8 20.2 61.5 7.7 30.8 21.9 69.2 0 30.8 28.9 0 53.9 46.1 15.8 15.4 38.5 46.1 23.5 30.8 23.1 46.1 28.0 46.1 7.8 46.1 30.2 53.9 0 46.1 7.6 0 46.2 53.8 3.7 30.8 15.4 53.8 2.3 38.5 7.7 53.8 11.6 30.8 7.7 61.5 6.0 38.5 0 61.5 5.8 0 30.8 69.2 1.9 These results are also plotted on a triangular diagram whlch appears as Fig. 1.
As can be seen from this diagram's right-hand corner, there is synergistic enhancement of detergency with mixtures containing diol and PAS only. The maximum occurs at around ' ' ' .
, Z~57/~6~
a 4:1 ratio of diol : PAS. If a limited amount of Synperonic A7 is introduced into such a mixture, the synergistic enhancement is still observed, but if the amount of Synperonic A7 is more than about 10% of the three surfactants, or the amount of PAS is less than 70% the mixtures are outside the scope of the invention and give relatively poorer triolein removal.
Analogously, there is a synergistic enhancement of detergency for mixtures containing diol and Synperonic only.
This is at the left-hand edge of the triangular diagram. If PAS is incorporated into such mixtures, detergency deteriorates. The requirements of this invention as stated originally circumscribe the area in which triolein removal is good.
. .
Roughly in the centre of the diagram is an area of improved detergency, falling within the scope of this invention. However it gives slightly less triolein removal than the areas at the left and right sides of the diagram which may therefore be preferred.
Example 4 Aqueous wash liquors were prepared containing the following materials in deionized water.
2C'57~62 Alkyl polyglycoside }
} one gram pe.r litre Dodecane 1,2-diol }
Sodium metaborate 0.05 molar These quantities would be typical of using 6g/litre of a detergent product containing 16~7% by weight surfactant.
The wash liquors had a pH of about lO resulting from the presence of the metaborate.
The alkylpolyglycoside was APG 300 from Horizon Chemical Co. This was of the formula Ro(G)x where R is a 9 to 11 carbon alkyl chain, G is glucose and x has an averaye value of 1.4. It had an HLB value of approximately 11 to 12. The dodecane 1,2-diol is available from Aldrich Chemical Co.
Wash liquors were prepared with various ratios of the two surfactants and used to wash polyester test cloths soiled with radiolabelled triolein. Washing was carried out at 40C for 20 minutes in a Tergotometer.
The removal of triolein was determined and the results were:
Z~57~6~
Ratio% Trio~ein removal APG 300/1,2-diol 100/0 58.9 95/5 60.2 90/10 58.5 80/20 41.2 60/40 4.5 40/60 2.2 20/80 1.7 0/100 1.7 Example 5 Example 4 was repeated using a different alkylpolyglycoside. APG 500 from Horizon was used. This has the formula Ro(G)x where R is Cl 2 and Cl 3 alkyl, G is glucose and x is 1.4. It had an HLB value of approximately 11.5 to 12.5.
Results were:
20 Ratio% Triolein removal APG 500:1,2-diol 100:0 45.3 90:10 54.1 80:20 37.1 60:40 6.2 40:60 2.3 20:80 1.8 0:100 1.7 21 2~57~62 Example 6 The procedure of Example 1 was repeated using as detergent active various proportions of an alkylpolyglycoside and Dodecane 1,2-diol. The alkylpolyglycoside was APG 550 from Horizon. This is of the general formula Ro(G)x where R is a 12 and 13 carbon atom alkyl chain, G is glucose and x has an average value of 1.8. It had an HLB value of approximately 12 to 13.
The compositions were added to 24FH water at a concentration of 6g/litre. The resulting wash liquors had a pH of 10 and were used to wash polyester test cloths as in previous Examples. The cloths came from a different batch, conseguently these figures cannot be compared directly with the results from Example 1.
Results were:
Ratio% Triolein removal APG 550:1,2-diol 100:0 43.5 92:8 58.0 85:15 32.2 69:31 5.9 54:46 2.6 22 ZC~57~62 Example 7 The previous Example 6 was repeated, using various m:ixtures of Synperonic A7 and APG 550 as the nonionic surfactant. The results, including these of the previous Example are given in the following table in which the amounts of APG 550, Dodecane 1,2-diol and Synperonic A7 are expressed as percentages of the total quantity of all three (which was a constant 13% of the overall composition). The results are also plotted as a triangular diagram which appears as Fig. 2.
2C'S~L6~
APG 550 Synperonic A7 C1 2 1,2 Diol~ Triolein Removal 0 100 0 68.9 15.4 84.6 0 66.9 30.8 69.2 0 64.2 50.0 50.0 0 62.5 69.2 30.8 ~ 57.~
100 0 0 43.5 80.8 11.5 7.7 63.3 92.3 0 7.7 58.0 0 84.6 15.4 74.5 23.1 61.5 15.4 68.0 53.8 30.8 15.4 63.8 69.2 15.4 15.4 58.5 84.6 0 15.4 32.2 0 69.2 30.8 62.7 15.4 53.8 30.8 59.2 23.1 46.1 30.8 55.0 38.4 30.8 30.8 47.8 69.2 0 30.8 5.9 0 53.8 46.2 13.6 23.1 30.8 46.2 11.3 38.4 15.4 46.2 8.7 53.8 0 46.2 2.6 It can be seen from this triangular diagram that for all proportions of APG 550: Synperonic A7, there iS a mixture with diol which gives greater triolein removal than without the diol.
2C~S7~6~
Example 8 Compositions were prepared having as a general formulation:
~ by weight Detergent active 17 Zeolite 32 Sodium silicate 0.8 Sokolan CP5 4.0 10 Sodium carbonate (anhydrous) 14.5 Sodium metaborate 16.5 The detergent active was provided by various proportions of alkylpolyglycoside, and dodecane 1,2-diol and coconut alkyl sulphate (PAS). The alkylpolyglycoside was APG 600 from Horizon (also available as Plantaren APG 600 from Henkel). This is of the general formula Ro(G)x where R is a coconut alkyl chain (i.e. principally C1 2 and Cl4), G is glucose and x has an average value of 1.4. It has an HLB value of approximately 12.
The compositions were added to 24 FH water at a concentration of 5 g/litre and used to wash polyester test cloths by the procedure as in Examples 1 and 2.
25Z~S7~62 Results were:
Ratio % Triolein removal PAS : APG 600 : 1,2-diol 0.0 100.0 0.0 60.3 25.0 75.0 000 49.2 50.0 50.00 0.0 50.1 75.0 25.0 0.0 46.5 100.0 0.0 0.0 53.8 0,O 93,0 7.0 66.7 109.3 83.7 7.0 59.1 93.0 0.0 7,0 61.0 0.0 86.0 14.0 70.0 , 17.2 68.8 14.0 63.3 51.6 34.4 14.0 58.7 1568.8 17.2 14.0 54.7 86.0 0.0 1~.0 58.0 0.0 79.0 21.0 64.1 15.8 63.2 21.0 63.6 39.5 39.5 21.0 61.2 2051.7 27.3 21.0 55.1 79,0 0.0 21.0 52.0 ; 45.5 19.5 35.0 45.4 29.0 29.0 42.0 27.1 0.0 51.0 49.0 7.8 2551.0 0.0 49.0 13.9 0.0 30.0 70.0 1.7 30.0 0.0 70.0 3.0 , 26 2~57~6~:
Again it can be seen that incorporation of diol in limited amounts leads to improved triolein removal.
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Claims (8)
1. A detergent composition containing 2 to 50% by weight of a surfactant mixture which comprises i) a 1,2 diol of the general formula where R is a saturated or unsaturated hydrocarbon group containing 8 to 16 carbon atoms, ii) one or more surfactants selected from a) primary alkyl sulphates of formula Ra OSO3 M
in which Ra is a saturated, unsubstituted, branched or straight chain primary alkyl or alkenyl group containing 8 to 18 carbon atoms and M is a solubilizing cation; and/or b) nonionic surfactants with an HLB value of 10.5 or above;
with the amounts by weight of (i), (a) and (b) such that either the amount of (b) is greater than 50% of (i) and (ii) in which case (i) is from 5 to 40% of (i) and (ii) while (a) is not more than 25% of (i) and (ii), with the proviso that (i) is at least 10% of (i) and (ii) if (a) is from 15 to 25% of (i) and (ii);
or the amount of (b) is less than 40% of (i) and (ii) in which case (i) is at least 5% of (i) and (ii) while (a) is at least 70% of (i) and (ii) and (b) is less than 10% of (i) and (ii) or else (i) is from 20 to 40% of (i) and (ii) while (a):(b) ranges from 40:60 to 70:30;
and with the proviso that the amount by weight of any anionic non-soap surfactant in the composition, other than any said primary alkyl sulphate (a) is less than half the amount of said primary alkyl sulphate (a).
in which Ra is a saturated, unsubstituted, branched or straight chain primary alkyl or alkenyl group containing 8 to 18 carbon atoms and M is a solubilizing cation; and/or b) nonionic surfactants with an HLB value of 10.5 or above;
with the amounts by weight of (i), (a) and (b) such that either the amount of (b) is greater than 50% of (i) and (ii) in which case (i) is from 5 to 40% of (i) and (ii) while (a) is not more than 25% of (i) and (ii), with the proviso that (i) is at least 10% of (i) and (ii) if (a) is from 15 to 25% of (i) and (ii);
or the amount of (b) is less than 40% of (i) and (ii) in which case (i) is at least 5% of (i) and (ii) while (a) is at least 70% of (i) and (ii) and (b) is less than 10% of (i) and (ii) or else (i) is from 20 to 40% of (i) and (ii) while (a):(b) ranges from 40:60 to 70:30;
and with the proviso that the amount by weight of any anionic non-soap surfactant in the composition, other than any said primary alkyl sulphate (a) is less than half the amount of said primary alkyl sulphate (a).
2. A detergent composition according to claim 1 wherein the hydrocarbon group R is an alkyl or alkenyl group of 8 to 16 carbon atoms.
3. A detergent composition according to claim 1 wherein the nonionic surfactant (b) is ethoxylated primary alcohol.
4. A composition according to claim 1, claim 2 or claim 3 wherein amounts by weight are such that:
(i):(ii) ranges from 35:65 to 95:5 while the amount of (b) is at least 8 times the amount, if any, of (a).
(i):(ii) ranges from 35:65 to 95:5 while the amount of (b) is at least 8 times the amount, if any, of (a).
5. A composition according to claim 1, claim 2 or claim 3 wherein the amounts by weight are such that:
(i):(ii) ranges from 25:75 to 95:5 while the amount of (a) is at least 9 times the amount, if any, of (b).
(i):(ii) ranges from 25:75 to 95:5 while the amount of (a) is at least 9 times the amount, if any, of (b).
6. A detergent composition according to claim 1, claim 2 or claim 3 which also contains 7 to 70% by weight of detergency builder.
7. A method of cleaning which comprises contacting fabrics or other inanimate surface to be cleaned with a composition according to any one of the preceding claims, or a wash liquor comprising water and a composition according to claim 1, claim 2 or claim 3 added to the water in a quantity lying in a range from 0.5 to 50 grams per litre of water.
8. A detergent composition as claimed in claim 1 and substantially as described herein.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9027416.8 | 1990-12-18 | ||
GB909027416A GB9027416D0 (en) | 1990-12-18 | 1990-12-18 | Detergent composition |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2057462A1 true CA2057462A1 (en) | 1992-06-19 |
Family
ID=10687180
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002057462A Abandoned CA2057462A1 (en) | 1990-12-18 | 1991-12-11 | Detergent composition |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP0491531A1 (en) |
JP (1) | JPH04300998A (en) |
BR (1) | BR9105472A (en) |
CA (1) | CA2057462A1 (en) |
GB (1) | GB9027416D0 (en) |
ZA (1) | ZA919952B (en) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0593406A1 (en) * | 1992-10-13 | 1994-04-20 | The Procter & Gamble Company | Non-aqueous liquid detergent compositions |
DE4306899A1 (en) * | 1993-03-05 | 1994-09-08 | Henkel Kgaa | Floor cleaning products |
AU675833B2 (en) * | 1994-03-23 | 1997-02-20 | Amway Corporation | Concentrated all-purpose light duty liquid cleaning composition and method of use |
US5632780A (en) * | 1995-03-30 | 1997-05-27 | The Procter & Gamble Company | Dry cleaning and spot removal proces |
US5591236A (en) | 1995-03-30 | 1997-01-07 | The Procter & Gamble Company | Polyacrylate emulsified water/solvent fabric cleaning compositions and methods of using same |
US5547476A (en) * | 1995-03-30 | 1996-08-20 | The Procter & Gamble Company | Dry cleaning process |
US5630847A (en) * | 1995-03-30 | 1997-05-20 | The Procter & Gamble Company | Perfumable dry cleaning and spot removal process |
BR9607892A (en) | 1995-03-30 | 1999-06-01 | Procter & Gamble | Dry cleaning item |
US5630848A (en) * | 1995-05-25 | 1997-05-20 | The Procter & Gamble Company | Dry cleaning process with hydroentangled carrier substrate |
US5912408A (en) | 1995-06-20 | 1999-06-15 | The Procter & Gamble Company | Dry cleaning with enzymes |
US5687591A (en) | 1995-06-20 | 1997-11-18 | The Procter & Gamble Company | Spherical or polyhedral dry cleaning articles |
EP0805200B1 (en) * | 1996-05-03 | 2003-07-16 | The Procter & Gamble Company | Hard surface cleaning compositions |
WO1998016611A1 (en) * | 1996-10-11 | 1998-04-23 | The Procter & Gamble Company | Laundry bar compositions comprising dihydric alcohol |
ATE301737T1 (en) | 1999-10-16 | 2005-08-15 | Ciba Sc Pfersee Gmbh | COMPOSITION FOR THE PRETREATMENT OF FIBER MATERIALS |
JP4629354B2 (en) * | 2004-02-25 | 2011-02-09 | 三洋化成工業株式会社 | Surfactant composition |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2679482A (en) * | 1949-10-08 | 1954-05-25 | Colgate Palmolive Co | Synthetic detergent compositions |
US3705113A (en) * | 1968-10-24 | 1972-12-05 | Chevron Res | Hydrogenated olefin sulfonate-alkyl-1,2-glycol detergent compositions |
US3766062A (en) * | 1971-08-03 | 1973-10-16 | Colgate Palmolive Co | 1,2-alkanediol containing fabric softening compositions |
US4692277A (en) * | 1985-12-20 | 1987-09-08 | The Procter & Gamble Company | Higher molecular weight diols for improved liquid cleaners |
JPH0759716B2 (en) * | 1986-08-29 | 1995-06-28 | ライオン株式会社 | Surfactant composition with reduced skin irritation |
JP2571117B2 (en) * | 1989-02-03 | 1997-01-16 | 花王株式会社 | Detergent composition |
DE3904610A1 (en) * | 1989-02-16 | 1990-08-23 | Henkel Kgaa | DETERGENT FOR WASHING POWER SUPPLEMENTS |
-
1990
- 1990-12-18 GB GB909027416A patent/GB9027416D0/en active Pending
-
1991
- 1991-12-11 CA CA002057462A patent/CA2057462A1/en not_active Abandoned
- 1991-12-13 EP EP19910311635 patent/EP0491531A1/en not_active Withdrawn
- 1991-12-17 BR BR919105472A patent/BR9105472A/en unknown
- 1991-12-18 ZA ZA919952A patent/ZA919952B/en unknown
- 1991-12-18 JP JP3335296A patent/JPH04300998A/en active Pending
Also Published As
Publication number | Publication date |
---|---|
ZA919952B (en) | 1993-06-18 |
GB9027416D0 (en) | 1991-02-06 |
EP0491531A1 (en) | 1992-06-24 |
BR9105472A (en) | 1992-09-01 |
JPH04300998A (en) | 1992-10-23 |
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