IE55427B1 - Fatty acid containing detergent compositions - Google Patents
Fatty acid containing detergent compositionsInfo
- Publication number
- IE55427B1 IE55427B1 IE1206/83A IE120683A IE55427B1 IE 55427 B1 IE55427 B1 IE 55427B1 IE 1206/83 A IE1206/83 A IE 1206/83A IE 120683 A IE120683 A IE 120683A IE 55427 B1 IE55427 B1 IE 55427B1
- Authority
- IE
- Ireland
- Prior art keywords
- alkyl
- composition
- carbon atoms
- weight
- compositions
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 79
- 239000003599 detergent Substances 0.000 title claims abstract description 27
- 235000014113 dietary fatty acids Nutrition 0.000 title claims abstract description 24
- 239000000194 fatty acid Substances 0.000 title claims abstract description 24
- 229930195729 fatty acid Natural products 0.000 title claims abstract description 24
- 150000004665 fatty acids Chemical class 0.000 title claims abstract description 22
- 239000004064 cosurfactant Substances 0.000 claims abstract description 16
- 239000003945 anionic surfactant Substances 0.000 claims abstract description 13
- 239000007788 liquid Substances 0.000 claims abstract description 13
- 102000004190 Enzymes Human genes 0.000 claims abstract description 7
- 108090000790 Enzymes Proteins 0.000 claims abstract description 7
- 239000004094 surface-active agent Substances 0.000 claims description 36
- 125000004432 carbon atom Chemical group C* 0.000 claims description 31
- -1 alkylbenzene sulfonate Chemical class 0.000 claims description 28
- 125000000217 alkyl group Chemical group 0.000 claims description 26
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 13
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 12
- 125000000129 anionic group Chemical group 0.000 claims description 11
- 125000005211 alkyl trimethyl ammonium group Chemical group 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 9
- 150000008051 alkyl sulfates Chemical class 0.000 claims description 7
- 229940088598 enzyme Drugs 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 6
- 244000060011 Cocos nucifera Species 0.000 claims description 5
- 235000013162 Cocos nucifera Nutrition 0.000 claims description 5
- 108091005804 Peptidases Proteins 0.000 claims description 5
- 239000004744 fabric Substances 0.000 claims description 5
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 claims description 5
- 229920006395 saturated elastomer Polymers 0.000 claims description 5
- 102000013142 Amylases Human genes 0.000 claims description 4
- 108010065511 Amylases Proteins 0.000 claims description 4
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- 150000001340 alkali metals Chemical class 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical class CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 claims description 4
- MPNXSZJPSVBLHP-UHFFFAOYSA-N 2-chloro-n-phenylpyridine-3-carboxamide Chemical compound ClC1=NC=CC=C1C(=O)NC1=CC=CC=C1 MPNXSZJPSVBLHP-UHFFFAOYSA-N 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 238000004900 laundering Methods 0.000 claims description 3
- 239000012188 paraffin wax Substances 0.000 claims description 3
- CXRFDZFCGOPDTD-UHFFFAOYSA-M Cetrimide Chemical compound [Br-].CCCCCCCCCCCCCC[N+](C)(C)C CXRFDZFCGOPDTD-UHFFFAOYSA-M 0.000 claims description 2
- 102000035195 Peptidases Human genes 0.000 claims description 2
- 239000004365 Protease Substances 0.000 claims description 2
- 235000019418 amylase Nutrition 0.000 claims description 2
- 229940025131 amylases Drugs 0.000 claims description 2
- 239000007864 aqueous solution Substances 0.000 claims description 2
- 150000001768 cations Chemical class 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- KAOPHVRFVWFGRN-UHFFFAOYSA-M decyl(trimethyl)azanium;methyl sulfate Chemical group COS([O-])(=O)=O.CCCCCCCCCC[N+](C)(C)C KAOPHVRFVWFGRN-UHFFFAOYSA-M 0.000 claims description 2
- DDXLVDQZPFLQMZ-UHFFFAOYSA-M dodecyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)C DDXLVDQZPFLQMZ-UHFFFAOYSA-M 0.000 claims description 2
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims 2
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical class CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 claims 1
- 150000003863 ammonium salts Chemical class 0.000 claims 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 18
- 239000002736 nonionic surfactant Substances 0.000 abstract description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 16
- 239000002689 soil Substances 0.000 description 11
- 125000001453 quaternary ammonium group Chemical group 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- 150000004985 diamines Chemical class 0.000 description 7
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 6
- POULHZVOKOAJMA-UHFFFAOYSA-N methyl undecanoic acid Natural products CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 6
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical class [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- 150000002402 hexoses Chemical class 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 125000001424 substituent group Chemical group 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 3
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229960004106 citric acid Drugs 0.000 description 3
- 239000003240 coconut oil Substances 0.000 description 3
- 235000019864 coconut oil Nutrition 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 239000003760 tallow Substances 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- TWJNQYPJQDRXPH-UHFFFAOYSA-N 2-cyanobenzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1C#N TWJNQYPJQDRXPH-UHFFFAOYSA-N 0.000 description 2
- BKOOMYPCSUNDGP-UHFFFAOYSA-N 2-methylbut-2-ene Chemical group CC=C(C)C BKOOMYPCSUNDGP-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QJRVOJKLQNSNDB-UHFFFAOYSA-N 4-dodecan-3-ylbenzenesulfonic acid Chemical compound CCCCCCCCCC(CC)C1=CC=C(S(O)(=O)=O)C=C1 QJRVOJKLQNSNDB-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Natural products CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 235000021360 Myristic acid Nutrition 0.000 description 2
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- 150000001335 aliphatic alkanes Chemical group 0.000 description 2
- 150000004996 alkyl benzenes Chemical class 0.000 description 2
- 125000006177 alkyl benzyl group Chemical group 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- VKOBVWXKNCXXDE-UHFFFAOYSA-N ethyl stearic acid Natural products CCCCCCCCCCCCCCCCCCCC(O)=O VKOBVWXKNCXXDE-UHFFFAOYSA-N 0.000 description 2
- 239000004519 grease Substances 0.000 description 2
- 150000002430 hydrocarbons Chemical group 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- AOHAPDDBNAPPIN-UHFFFAOYSA-N myristicinic acid Natural products COC1=CC(C(O)=O)=CC2=C1OCO2 AOHAPDDBNAPPIN-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N n-hexadecanoic acid Natural products CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 230000003472 neutralizing effect Effects 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 235000011118 potassium hydroxide Nutrition 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 150000003871 sulfonates Chemical class 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- NKFNBVMJTSYZDV-UHFFFAOYSA-N 2-[dodecyl(2-hydroxyethyl)amino]ethanol Chemical compound CCCCCCCCCCCCN(CCO)CCO NKFNBVMJTSYZDV-UHFFFAOYSA-N 0.000 description 1
- LBLYYCQCTBFVLH-UHFFFAOYSA-M 2-methylbenzenesulfonate Chemical compound CC1=CC=CC=C1S([O-])(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-M 0.000 description 1
- PZNSXEGDODLWLT-UHFFFAOYSA-M 3-decoxypropyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCOCCC[N+](C)(C)C PZNSXEGDODLWLT-UHFFFAOYSA-M 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241001522296 Erithacus rubecula Species 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 239000004280 Sodium formate Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 125000005192 alkyl ethylene group Chemical group 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000010480 babassu oil Substances 0.000 description 1
- 235000015241 bacon Nutrition 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006172 buffering agent Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 235000019219 chocolate Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 150000004656 dimethylamines Chemical class 0.000 description 1
- WWYHAQDAMPXWSI-UHFFFAOYSA-N dodecan-1-ol;methane Chemical compound C.CCCCCCCCCCCCO WWYHAQDAMPXWSI-UHFFFAOYSA-N 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
- ILDUKHDOZROSQN-UHFFFAOYSA-L dodecyl-dimethyl-[2-(trimethylazaniumyl)ethyl]azanium;dichloride Chemical compound [Cl-].[Cl-].CCCCCCCCCCCC[N+](C)(C)CC[N+](C)(C)C ILDUKHDOZROSQN-UHFFFAOYSA-L 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000007046 ethoxylation reaction Methods 0.000 description 1
- 125000005313 fatty acid group Chemical group 0.000 description 1
- 229940013317 fish oils Drugs 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 235000013882 gravy Nutrition 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 239000003752 hydrotrope Substances 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-N methyl sulfate Chemical class COS(O)(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-N 0.000 description 1
- NQMRYBIKMRVZLB-UHFFFAOYSA-N methylamine hydrochloride Chemical compound [Cl-].[NH3+]C NQMRYBIKMRVZLB-UHFFFAOYSA-N 0.000 description 1
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- HVOYZOQVDYHUPF-UHFFFAOYSA-N n,n',n'-trimethylethane-1,2-diamine Chemical compound CNCCN(C)C HVOYZOQVDYHUPF-UHFFFAOYSA-N 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000003605 opacifier Substances 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000003346 palm kernel oil Substances 0.000 description 1
- 235000019865 palm kernel oil Nutrition 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
- 229960003330 pentetic acid Drugs 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 1
- 229960003656 ricinoleic acid Drugs 0.000 description 1
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 1
- 239000003813 safflower oil Substances 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 235000015067 sauces Nutrition 0.000 description 1
- HLBBKKJFGFRGMU-UHFFFAOYSA-M sodium formate Chemical compound [Na+].[O-]C=O HLBBKKJFGFRGMU-UHFFFAOYSA-M 0.000 description 1
- 235000019254 sodium formate Nutrition 0.000 description 1
- KVCGISUBCHHTDD-UHFFFAOYSA-M sodium;4-methylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1 KVCGISUBCHHTDD-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001180 sulfating effect Effects 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- CMQCNTNASCDNGR-UHFFFAOYSA-N toluene;hydrate Chemical compound O.CC1=CC=CC=C1 CMQCNTNASCDNGR-UHFFFAOYSA-N 0.000 description 1
- 125000005209 triethanolammonium group Chemical class 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 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
- C11D10/00—Compositions of detergents, not provided for by one single preceding group
- C11D10/04—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/42—Amino alcohols or amino ethers
- C11D1/44—Ethers of polyoxyalkylenes with amino alcohols; Condensation products of epoxyalkanes with amines
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/62—Quaternary ammonium 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
- C11D1/38—Cationic compounds
- C11D1/65—Mixtures of anionic with cationic compounds
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/75—Amino oxides
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- 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
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3711—Polyacetal carboxylates
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- 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
- C11D3/38—Products with no well-defined composition, e.g. natural products
- C11D3/386—Preparations containing enzymes, e.g. protease or amylase
- C11D3/38618—Protease or amylase in liquid compositions only
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- 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
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- 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
- C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
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- 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
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Abstract
Detergent compositions, preferably heavy-duty liquids, containing an anionic surfactant, a selected cosurfactant and a fatty acid are disclosed. The compositions are formulated to provide an initial pH of from about 6.0 to about 8.5 at a concentration of from about 0.1% to about 2% by weight in water at 20 DEG C. The compositions preferably also contain ethoxylated nonionic surfactants, a detergent builder and enzymes.
Description
2 2 5¾ 4 Z~< The present invention relates to detergent compositions, preferably liquid detergents, containing an anionic synthetic surfactant, a cosurfactant selected from certain quaternary ammonium, diquaternary ammonium, amine b ana diamine surfactants, and a fatty acid. The compositions herein have a molar ratio of the anionic synthetic surfactant to the cosurfactant of at least 1 and are formulated to provide an initial pH of from 6.0 to 8.5 at a concentration of from 0.1% to 2% by weight in 10 water at 20°C. The compositions provide both superior greasy/ oily soil removal and good builder/pH sensitive soil removal at the near-neutral wash pH.
U.S. Patent 4,285,841, Barrat et al_, issued August 25, 1981 , discloses liquid detergents containing anionic surfactants, nonionic 15 surfactants and from about 8% to about 20% by weight of a fatty acid. The compositions have a pH of from about 6.0 to 7.5.
U.S. Patent 4,287,082, Toifo et_al, issued September 1, 1981, discloses liquid detergents containing saturated fatty acids, enzymes, enzyme-accessible calcium and selected short-chain 2u carboxylic acids.
U.S. Patent 4,321,165, Smith et. at., issued March 23, 1982, discloses built detergents containing anionic, nonionic and cationic surfactants. The compositions provide a solution pH of at least about 6, and preferably greater than about 8.
The present invention encompasses detergent compositions comprising: (a) from 2% to 60% by weight of an anionic synthetic surfactant; (b) from 0.25% to 12% by weight of a cosur- 30 factant selected from: 3 (i) quaternary ammonium surfactants having the formula: [R2(OR3) l[R4(OR3) 1,RSN+X" 2 y y * wherein R is an alkyl or alkyl benzyl group having from 8 5 to 18 carbon atoms in the alkyl chain; each R3 is selected from -CH2CH2t, -CH2CH(CH3)-, -CH2CH(CH2OH)-, -CK2CH2CH2" and mixtures thereof; each R4 is selected from hydrogen (provided that y is not 0), C1-4 alkyl, hydr- oxyalkyl, benzyl, ring structures formed by joining the two 10 R4 groups. and -CH2C3JCHCHOHCDR^CHCHCU2OH wherein R*’ is any hexose or hexose polymer having a molecular weight up to 5 4 1000; R is the same as R or is 2 an alkyl chain wherein the total number of carbon atoms of R plus R5 is not more than 18; each y is from 0 to 10 15 and the sum of the y values is from 0 to 15; and X is any compatible anion; (ii) diquaternary ammonium surfactants having the formula: [ R2(OR3) ] [R4(OR3) ]-N+R3N+R3[ R4(OR3) ], (X')2 20 wherein R , R , R , R , y and X are as defined above; (iii) amine surfactants having the formula: [R2(OR3) l[R4(OR3) 1RSN 2 3iiS' / wherein R , R , R , R and y are as defined above; and (iv) diamine surfactants having the formula: 25 [R2(OR3) 1[r"(OR3) 1NR3NR5[r\0R3) ] \2 3 4 y s y wherein R , R , R , R and y are as defined above; and (c) from 5% to 40% by weight of a fatty acid containing from 10 to 22 carbon atoms and from 0 to 10 .ethylene oxide units in the hydrocarbon chain; 4 said composition having a molar ratio of the anionic synthetic surfactant to the cosurfactant of at least 1 and formulated to provide an initial pH of from 6.0 to 8.5 at a concentration of from 0.1% to 2% by weight in water at 20°C.
The detergent compositions herein contain an anionic synthetic surfactant, a cosurfactant selected from certain quaternary ammonium, diquaternary ammonium, amine and diamine surfactants, and a fatty acid material. The compositons can be in any form, including granules, liquids, tablets or pastes. However, liquid compositions are highly preferred since the compositions herein are especially effective when applied directly to soils and stains in a pretreatment step. The compositions herein must have a molar ratio of the anionic synthetic surfactant to the cosurfactant of at least one, preferably from 2:1 to 20:1, and are formulated to provide an initial pH of from 6,0 to 8.5 at a concentration of from 0.1% to 2% by weight in water at 20°C. It has been found that the addition of the cosurfactant to the fatty acid containing detergents herein provides important greasy/oily soil removal benefits only at the near-neutral wash pH. The wash pH is preferably from 7.0 to 8.5, more preferably from 7.5 to 8.0.
While not intending to be limited by theory, it is believed that the cosurfactant and anionic surfactant herein form complexes which enhance packing of the surfactants at the oil/water interface, thereby lowering interfacial tension and improving detergency. (The amine and diamine surfactants would be at least partially protonated at the near-neutral pH and thus can form charged species capable of complex-ing with the anionic surfactant.) At the defined pH range recited herein, the fatty acid component exists in a chemical form which is optimal for effective detergency. At too low a pH, the non-dissociated form of the acid is ineffective, It is also believed that the higher pH's (i.e., above 8.5) affect the interaction 5 of the fatty acid with the cosurfactant and water hardness and result in the formation of undesirable species at the oil/water interface which reduce detergency performance.
Anionic Synthetic Surfactant 5 The detergent compositions herein contain from 2% to 60% by weight of an anionic synthetic surfactant, or mixtures thereof. The anionic surfactant preferably represents from 5% to 40%, and more preferably from 10% to 20%, by weight of the detergent composition. Anionic sur-10 factants useful herein are disclosed in U.S. Patent 4,285,841, Barrat _et _al_, issued August 25, 1981, and in U.S. Patent 3,919,678, Lauqhlin et al. issued December 30, 1975.
Useful anionic surfactants include the water-soluble salts, particularly the alkali metal, ammonium and alkylolammonium 15 (e.g., monoethanolammonium or triethanolammonium) salts, of organic sulfuric reaction products having in their molecular structure an alkyl group containing from 10 to 20 carbon atoms and a sulfonic acid or sulfuric acid ester group. (Included in the term "alkyl" is the alkyl portion of aryl groups.) 20 Examples of this group of synthetic surfactants are the alkyl sulfates, especially those obtained by sulfating the higher alcohols (Cg-C|8 carbon atoms) such as those produced by reducing the glycerides of tallow or coconut oil; and the alkylbenzene sulfonates in which the alkyl group contains from 9 to 15 25 carbon atoms, in straight chain or branched chain configuration, e.g., those of the type described in United States Patents 2,220,099 and 2,477,383. Especially valuable are linear straight chain alkylbenzene sulfonates in which the average number of carbon atoms in the alkyl group is from 11 to 14.
Other anionic surfactants herein are the water-soluble salts of; paraffin sulfonates containing from 8 to 24 (pre ferably 12 to 18) carbon atoms; alkyl glyceryl ether sulfonates, especially those ethers of alcohols (e.g., those derived from tallow and coconut oil); alkyl phenol ethylene oxide 8 ether sulfates containing from | to 4 units of ethylene oxide per molecule and from 8 to 12 carbon atoms in the alkyl group; and alkyl ethylene oxide ether sulfates containing 1 to 4 units of ethylene oxide per molecule and from 10 to 20 carbon atoms in the alkyl group.
Other useful anionic surfactants herein include the water-soluble salts of esters of α-sulfonated fatty acids containing from 6 to 20 carbon atoms in the fatty acid group and from 1 to 10 carbon atoms in the ester group; water-soluble salts of 2-acyloxy-alkane-l-sulfonic acids containing from 2 to 9 carbon atoms in the acyl group and from 9 to 23 carbon atoms in the alkane moiety; water-soluble salts of olefin sulfonates containing from I2 to 24 carbon atoms; and B-alkyloxy alkane sulfonates containing from I to 3 carbon atoms in the alkyl group and from 8 to 20 carbon atoms in the alkane moiety.
Particularly preferred anionic surfactants herein are the alkyl sulfates of the formula R0(C2H40)xS03M+ wherein R is an alkyl chain having from 8 to 18 carbon atoms, saturated or unsaturated, and the longest linear portion of the alkyl chain is 15 carbon atoms or less on the average, M is a cation which makes the compound water-soluble, especially an alkali metal, ammonium or substituted ammonium cation, and x is from 0 to 4. Most preferred are the non-ethoxylated ^ primary and secondary alkyl sulfates. Under cold water washing conditions, i.e., less than 65°F (18.3°C), it is preferred that there be a mixture of such alkyl sulfates.
Mixtures of the alkyl sulfates with the above-described alkylbenzene sulfonates, paraffin sulfonates, alkyl glyceryl ether sulfonates and esters of a α-sulfonated fatty acids, particularly with the ^i_i3 l*near alkylbenzene sulfonates, are also preferred.
Cosurfactant 7 The compositions herein also contain from 0.25¾ to 12%, preferably from 0.5% to 8%, more preferably from 1% to 4%, by weight of a cosurfactant selected from certain quarternary ammonium, diquaternary ammonium, amine and diamine surfactants. The quaternary ammonium surfactants are particularly preferred.
The quaternary ammonium surfactants herein are of the formula: [R2(OR3) l[R4(OR3) ],R5N+X" 2 y y L wherein R is an alkyl or alkyl benzyl group having from 8 3 to 18 carbon atoms in the alkyl chain; each R is selected from -CH2CH2-, -CH2CH(CH3)-, -CH2CH(CH2OH)-, -CH2CH2CH2-, and mixtures thereof; each R4 is selected from Ci-4 Ci-4 hydroxy - alkyl, benzyl, ring structures formed by joining the two R4 groups, -CH2CHOHCHOHCOR6CHOHCH2OH wherein R6 is any hexose or hexose polymer having a molecular weight less than 5 4 1000, and hydrogen when y is not 0; R is the same as R or is an alkyl chain wherein the total number of carbon atoms of R2 plus R3 is not more than 18; each y is from 0 to 10 and the sum of the y values is from 0 to 15; and X is any compatible anion.
Preferred of the above are the alkyl quaternary ammonium surfactants, especially the mono-long chain alkyl surfactants 5 described in the above formula when R is selected from the same If groups as R . The most preferred quaternary ammonium surfactants are the chloride, bromide and methylsulfate Cg1(. alkyl trimethylammonium salts, ^8-16 alkyl di(hydroxyethyl)methyiammonium salts, the Cgl(. alkyl hydroxyethyldimethylammonium salts, and Cg alkyloxypropyl trimethylammonium salts. Of the above, decyl trimethylammonium methylsulfate, lauryl trimethylammonium chloride, myristyl trimethylammonium bromide and coconut trimethylammonium chloride and methylsulfate are particularly preferred. 8 Under cold water washing conditions, i.e., less than 65°F (18.3°C), the Cg_^ alkyltrimethyl ammonium surfactants are particularly - preferred since they have a lower Kraft boundry and, therefore, a lower crystallization temperature than the 5 longer alkyl chain quaternary ammonium surfactants herein.
Diquaternary ammonium surfactants herein are of the formula: [R2(OR3] HR^OR3) 1,N+R3N+R5IR4(0R3) 1 (ΧΊ, / ? 3*4 5 * wherein the R , R , R , R , y and X substituents are as defined 10 above for the quaternary ammonium surfactants. These substituents are also preferably selected to provide diquaternary ammonium surfactants corresponding to the preferred quaternary ammonium surfactants. Particularly preferred are the Cg_lg alkyl pentamethylethylenediammonium chloride, bromide and 15 methylsulfate salts.
Amine surfactants useful herein are of the formula: [R2(OR3)v1[R4(OR3) 1R5N 2 3 Ψ 5 ' wherein the R , R , R , R and y substituents are as defined above for the quaternary ammonium surfactants. Particularly 20 preferred are the Cj2-16 dimethyl amines.
Diamine surfactants herein are of the formula [R2[OR3l HrW3)JNRWtR^COR3) 1 y 2 3 y 4 5 y wherein the R , R , R , R and y substituents are as defined above. Preferred are the ^12-16 a'kyl trimethylethylene 25 diamines. 9 Fatty Acid- The compositions of the present invention contain from 5% to 40%, preferably from 7% to 30%, most preferably from 10% to 20%, by weight of a fatty acid 5 containing from 10 to 22 carbon atoms. The fatty acid can also contain from 1 to 10 ethylene oxide units in the hydrocarbon chain.
Suitable fatty acids are saturated and/or unsaturated and can be obtained from natural sources such as plant or animal 10 esters (e.g., palm kernel oil, palm oil, coconut oil, babassu oil, safflower oil, tall oil, castor oil, tallow and fish oils, grease, and mixtures thereof) or synthetically prepared (e.g., via the oxidation of petroleum or by hydrogenation of carbon monoxide via the Fisher-Tropsch process). Examples of suitable saturated 15 fatty acids for use in the compositions of this invention; include capric, lauric, myristic, palmitic, stearic, arachidic and behenic acid. Suitable unsaturated fatty acid species include: palmitoleic, oleic, linoleic, iinolenic and ricinoleic acid. Examples of preferred fatty adds are saturated C^-C^ (coconut) fatty 20 acids, from 5:1 to 1:1 (preferably 3:1 ) weight ratio mixtures of lauric and myristic acid, and mixtures of the above lauric/myristic blends with oleic acid at a weight ratio of 4:1 to 1:4 mixed lauric/myristic : oleic.
Optional Components 25 The compositions of the present invention also preferably contain up to 30%, preferably from 1% to 20%, more preferably from 5% to 15%, by weight of an ethoxylated nonionic surfactant. These materials are described in U.S. Patent 4,285,841 , Barrat et at, issued August 25, 1981. 30 Preferred are the ethoxylated alcohols and ethoxylated alkyl phenols of the formula R(OC2H1()nOH, wherein E is selected from aliphatic hydrocarbon radicals containing from 8 to 15 carbon atoms and alkyl phenyl radicals in which the alkyl groups 35 contain from 8 to 12 carbon atoms, n is from 3 10 to 9, and said nonionic surfactant has an HLB (hydrophile-lipophile balance) value of from 10 to 13. These surfactants are more fully described in U.S. Patent 4,289,532, Leikhim et_jal, issued August 18, 1981.
Particularly preferred are ethoxylated alcohols having an average of from 10 to 15 carbon atoms in the alcohol and an average degree of ethoxylation of from 3 to 8 moles of ethylene oxide per mole of alcohol.
The compositions herein also preferably contain up to 40%, more preferably from 1% to 30%, by weight of a detergent builder material. While all manner of detergent builders known in the art can be used in the present compositions, the type and level of builder must be selected such that the final composition has an initial pH of from 6.0 to 8.5 at a concentration of from 0.1% to 1% by weight in water at 20°C. Detergent builders are described in U.S. Patent 4,321.165, Smith _et _al_, issued March 23, 1982.
In the preferred liquid detergent compositions herein, the builder preferably represents from 1% to 20%, more preferably from 3% to 10%, by weight of the composition. Preferred builders for use in liquid detergents herein are described in U.S. Patent 4,284,532, Leikhim et al, issued August 18, 1981.
A particularly preferred builder is citric acid.
Other preferred components for use in liquid detergents herein are the neutralizing agents, buffering agents, phase regulants, hydrotropes, enzymes, enzyme stabilizing agents, polyacids, suds regulants, opacifiers, antioxidants, bactericides, dyes, perfumes, and brighteners described in the U.S. Patent 4,285,841, Barrat et al, issued August 25, 1981.
Preferred neutralizing agents for use herein are organic bases, especially triethanolamine and monoethanolamine, which result in better detergency performance than inorganic bases such as sodium and potassium hydroxides. 11 Particularly preferred compositions herein contain from 0.1¾ to 2% by weight of detersive enzymes, especially the amylases, proteases, and mixtures thereof, of the type well known to detergent formulators.
The following non-limiting examples illustrate the compositions of the present invention. All percentages, parts and ratios used herein are by weight unless otherwise specified.
EXAMPLE I Four sets of 7.6 cm square polycotton (P/C) or cotton (C) swatches stained with standard soils were washed in an automatic mini-washer using 2000 ppm of either Composition A, a commercially available heavy-duty liquid detergent; Composition B containing, by weight, 6.2¾ sodium C.^ linear alkylbenzene sulfonate, 9.4% sodium alkyl sulfate, 10.0% alcohol polyethoxylate (6.5), 10.0% coconut fatty acid, 5.0% oleic fatty acid, 15.0% citric acid, 0.3% diethylenetriame pentamethylene phosphonic acid, 0.23% brightener, 1.0% protease enzyme, enough monoethanolamine to achieve the desired pH and the balance, to 100% water; Composition C, which was B plus 2.7% by weight of Cjj alkyl trimethylammonium chloride; or Composition D, which was B plus 2.7% by weight of C12_lg alkyl dimethyl amine oxide.
The wash pH was about 7.3 for Composition A and about 7.4 for B, C and D. The wash water temperature was 95°F (35°C) and the water hardness was 86mg/l (5 grains/gallon) (3:1 Ca :Mg ). The swatches were then dried and each set was round robin comparison graded against its counterparts to determine relative soil removal provided by the detergent compositions. A grading scale of -4 to 4 was used, with -4 indicating much less soil removal, 0 indicating no difference and 4 indicating much more soil removal. The results for each composition were then averaged and Composition A was assigned a relative value of 0.
A similar comparision was made except that the wash pH for Compositions B, C and D was about 9.5.
The results were as follows. 12 Wash pH 7,4 Wash pH 9.5 Ccnpcsition Soil Fabric Ξ C D B C D —- "* — — — — — Bacon grease P/C 0.1 1.6 0.9 0.6 0.7 0.5 Synthetic dir- P/C 0.1 1.9 2.6 -0.7 1.0 0.6 ty motor oil Makeup (oil P/C -0.5 1.5 1.6 -2.0 -1.7 -2.6 base) Spaghetti P/C -1.3 -1.7 -1.8 -0.5 -0.7 -0.1 sauce Chocolate C 1.5 1.0 -0.2 -0.4 -2.0 -2.0 Grass P/C -1.6 1.8 2.3 3.5 3.6 4.2 Gravy C 0.9 0.5 1.6 4.0 3.6 3.7 Clay P/C 2.2 3.7 3.3 -1.0 0.9 -0.8 Clay C 3.2 2.9 3.5 4.1 3.6 3.2 Body Soil P/C 0.6 0.4 0.5 0.8 1.3 0.8 The above results demonstrate that Composition C of the present invention containing quaternary ammonium cosurfactant provides important advantages on greasy/oil soils and also on grass and clay (on PC) relative to Composition B at wash pH's of 7.4. However, these advantages are substantially eliminated at wash pH's of 9.5.
As demonstrated above, the present invention also encompasses a method for laundering fabrics comprising contacting said fabrics with an aqueous solution having a pH of from 6.0 to 8.5 at 20°C and containing at least 0.1% by weight of the compositions herein.
EXAMPLE II Liquid detergent compositions of the present invention are as follows.
Component Wt. % A B C^j linear alkylbenzene sulfonic acid 5.8 5.5 Coconutalkyl sulfuric acid 8.8 8.3 Cj2 alkyl trimethylammonium chloride 1.2 C.^ alkyl trimethylammonium bromide - 1.7 C12 13 alcohol polyethoxylate (6.5) 10.0 - C13_l5 alcohol polyethoxylate (7) - 9.4 Laurie acid 7.5 7.1 Myristic acid 2.5 2.3 Oleic acid 5.0 4.7 Citric acid monohydrate Diethylenetriamine pentamethylene- 7.5 5.7 phosphonic acid 0.3 0.3 Diethylenetriamine pentaacetic acid 0.3 0.3 Protease enzyme 1.0 1.0 Amylase enzyme 0.3 0.3 Monoethanolamine 12.0 - T riethanolamine 6.7 7.5 Sodium hydroxide - 3.2 Potassium hydroxide - 4.0 1,2-Propanediol 5.0 8.5 Ethanol 1.0 4.7 Sodium formate 1.0 1.0 Sodium toluene sulfonate 5.0 - Minors and water Balance to 100 k 45% branched Composition A was prepared by adding the components, with continuous mixing, in the following order: alcohol polyethoxylate; monoethanolamine; premix of coconutalkyl sulfuric acid paste (containing propanediol, triethanolamine, coconutalkyl sulfuric acid, water and minors) and monoethanolamine-neutralized alkylbenzene sulfonic acid; premix of toluene sulfonate and water; citric acid; alkyl trimethylammonium chloride; premix of fatty acids; phosphonic acid; acetic acid; premix of dye, brightener, formate, ethanol and water; adjust pH to about 8.1 with monoethanolamine or water; protease enzyme; amylase enzyme; and perfume. The product obtained was a clear liquid. It exhibited better detergency performance than a similar product obtained by adding the fatty acids prior to adding the alkyltrimethylammonium chloride. The product also exhibited better detergency 14 performance, phase stability and a less objectionable base odor than a similar product obtained by adding the monoethanolamine after the premix of the coconutalkyl sulfuric acid paste and the neutralized alkylbenzene sulfonic acid.
Composition B was obtained by mixing the components.
Other compositions of the present invention are obtained when the alkyl trimethylammonium halides in the above compositions are replaced with coconutalkyl trimethylammonium chloride, decyi trimethylammonium methyisulfate, lauryl 10 difhydroxyethyl) methylammonium chloride, decyloxypropyl trimethylammonium chloride, lauryl pentamethylethylenediammonium chloride, lauryl diethanolamine cr coconutalkyl trimethylethylene diamine..
Other compositions herein are obtained when, in the above 15 compositions, the linear alkylbenzene sulfonic acid is replaced with coconutalkyl sulfuric acid or alkyl sulfuric acid, and when the coconutalkyl sulfuric acid is replaced with C14l5 alkyl ethoxy (1 avg.) sulfuric acid.
Compositions of the present invention are also obtained when 20 the lauric/myristic/oleic fatty acid mixture in the above compositions is replaced with coconut fatty acid or a 3:1 weight ratio mixture of lauric and myristic acid.
Granular detergents of the present invention can be obtained by spray-drying the above compositions and admixing heat-sensitive materials such as the enzymes.
Claims (13)
1. 2. The composition of Claim 1 wherein the anionic surfactant comprises an alkyl sulfate of the formula ROiC^O^SOgM* wherein R is an alkyl chain having from 8 to 18 carbon atoms, saturated or unsaturated, and the longest linear portion of the alkyl chain is 15 carbon atoms or less on the average, M is a cation which makes the compound water-soluble, and x is from 0 to 4.
2. 3. The composition of Claim 2 wherein in the alkyl sulfate surfactant, R is an alkyl group containing from 12 to 15 carbon atoms, x is 0 and M is an alkali metal, ammonium or substituted ammonium cation.
3. 4. The composition of Claim 3 wherein the anionic surfactant additionally comprises a water-soluble salt of an alkylbenzene sulfonate, paraffin sulfonate, alkyl glyceryl ether sulfonate or an ester of an α-sulfonated fatty acid.
4. 5. The composition of Claim 3 wherein the anionic surfactant additionally comprises an alkali metal, ammonium or substituted ammonium salt of a linear alkylbenzene sulfonate containing from 11 to 13 carbon atoms in the alkyl chain. 17
5. 6. The composition of Claim 1 wherein the cosurfactant is selected from the chloride, bromide and methylsulfate g alkyl trimethylammonium salts, Cg_1g alkyl di(hydroxyethyl) methylamrnonium salts, ^8-16 alkyl 5 hydroxyethyldimethylammonium salts, and Cg_lg alkyloxypropyl trimethylammonium salts.
6. 7. The compositions of Claim 6 wherein the cosurfactant is decyl trimethylammonium methylsulfate, lauryl trimethylammonium chloride, myristyl trimethylammonium bromide and coconut alkyl 10 trimethylammonium chloride and methylsulfate.
7. 8. The compositions of Claim 1 wherein the fatty acid comprises a material containing from 10 to 14 carbon atoms, or mixtures thereof.
8. 9. The compositions of Claim 3 wherein the cosurfactant is 15 selected from the chloride, bromide and methylsulfate Cg_1g alkyl trimethylammonium salts, Cg_lg alkyl di( hydroxy ethyl) methylamrnonium salts, Cg _lg alkyl hydroxyethyldimethylammonium salts, and Cg_1g alkyloxypropyl trimethylammonium salts, and the fatty 20 acid comprises a material containing from 10 to 14 carbon atoms, or mixtures thereof.
9. 10. A liquid detergent composition according to Claim 9 comprising from 10% to 20% by weight of the anionic synthetic surfactant, from 1% to 4% by weight of the 25 cosurfactant, and from 10% to 20% by weight of the fatty acid.
10. 11. The composition of Claim 10 additionally comprising from 0.1 to 2% by weight of an enzyme suitable for use in detergent compositions selected from amylases, proteases, and mixtures thereof. 30 18
11. 12. The composition of Claim 11 additionally comprising from 3% to 10% by weight of citric acid.
12. 13. A method for laundering fabrics comprising contacting said fabrics with an aqueous solution having a pH of 6.0 to 8.5 at 20°C and containing at least 0.1% by weight of the composition of Claim 1. 14. a detergent composition according to Claim 1, substantially as hereinbefore described with particular reference to the accompanying Examples.
13. 15. A method according to Claim 13 for laundering fabrics, substantially as hereinbefore described with particular reference to Example I of the accompanying Examples. F.R. KELLY & CO., AGENTS FOR THE APPLICANTS.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US38098882A | 1982-05-24 | 1982-05-24 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IE831206L IE831206L (en) | 1983-11-24 |
| IE55427B1 true IE55427B1 (en) | 1990-09-12 |
Family
ID=23503238
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IE1206/83A IE55427B1 (en) | 1982-05-24 | 1983-05-23 | Fatty acid containing detergent compositions |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP0095205B1 (en) |
| JP (1) | JPS5925894A (en) |
| AT (1) | ATE22920T1 (en) |
| AU (1) | AU559791B2 (en) |
| CA (1) | CA1208519A (en) |
| DE (1) | DE3366958D1 (en) |
| FI (1) | FI73727C (en) |
| GR (1) | GR78820B (en) |
| IE (1) | IE55427B1 (en) |
| MX (1) | MX162610A (en) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4507219A (en) * | 1983-08-12 | 1985-03-26 | The Proctor & Gamble Company | Stable liquid detergent compositions |
| US4747977A (en) * | 1984-11-09 | 1988-05-31 | The Procter & Gamble Company | Ethanol-free liquid laundry detergent compositions |
| SE8603087L (en) * | 1985-07-25 | 1987-01-26 | Colgate Palmolive Co | TEXTILE SOFTING AND ANTISTATIC DETERGENT COMPOSITION |
| SE8604714L (en) * | 1985-11-15 | 1987-05-16 | Colgate Palmolive Co | DETERGENT COMPOSITION WITH IMPROVED ABILITY TO REMOVE OILY DIRT |
| DE3614825A1 (en) * | 1986-05-02 | 1987-11-05 | Henkel Kgaa | USE OF ALKYLAMINOPOLYGLYKOLETHERS AS FOAM-PRESSING ADDITIVES IN LOW-FOAM CLEANING AGENTS |
| US4704221A (en) * | 1986-10-22 | 1987-11-03 | The Procter & Gamble Company | Granular detergents which contain high levels of anionic surfactant that forms a middle-phase, surface treated with a water soluble cationic surfactant |
| EP0495554A1 (en) * | 1991-01-16 | 1992-07-22 | The Procter & Gamble Company | Detergent compositions with high activity cellulase and quaternary ammonium compounds |
| DE69509068T2 (en) * | 1994-01-25 | 1999-11-18 | The Procter & Gamble Co., Cincinnati | LONG-CHAIN AMINOXYD CONTAINING, HIGH-FOAMING, MOLD, LIQUID OR GEL-MOLDED DETERGENT COMPOSITIONS |
| EP0741770A1 (en) * | 1994-01-25 | 1996-11-13 | The Procter & Gamble Company | Low sudsing detergent compositions containing long chain amine oxide and branched alkyl carboxylates |
| US5466394A (en) * | 1994-04-25 | 1995-11-14 | The Procter & Gamble Co. | Stable, aqueous laundry detergent composition having improved softening properties |
| CA2188766A1 (en) * | 1994-04-25 | 1995-11-02 | Francesco De Buzzaccarini | Stable, aqueous laundry detergent composition having improved softening properties |
| JPH09512850A (en) * | 1994-05-10 | 1997-12-22 | ザ、プロクター、エンド、ギャンブル、カンパニー | Heavy duty liquid laundry detergent composition containing anionic surfactant, amine oxide surfactant and fatty acid |
| US6017874A (en) * | 1995-09-29 | 2000-01-25 | The Procter & Gamble Company | Liquid laundry detergents containing selected quaternary ammonium compounds |
| WO1997012022A1 (en) * | 1995-09-29 | 1997-04-03 | The Procter & Gamble Company | Stable aqueous laundry detergent compositions comprising quaternary surfactants and amine oxides and having improved suspension properties |
| AU3824195A (en) * | 1995-09-29 | 1997-04-17 | Procter & Gamble Company, The | Liquid laundry detergents containing selected quaternary ammonium compounds |
| AR003724A1 (en) * | 1995-09-29 | 1998-09-09 | Procter & Gamble | STRUCTURED LIQUID LAUNDRY DETERGENT COMPOSITION, FOR HARD WORK, COMPRISING ANIONIC AND CATIONIC SURFACTANTS. |
| AR003725A1 (en) * | 1995-09-29 | 1998-09-09 | Procter & Gamble | LIQUID DETERGENT COMPOSITIONS CONTAINING AN AMINE, ALKYL SULPHATE AND ADDITIONAL ANIONIC SURFACTANT. |
| MA25183A1 (en) * | 1996-05-17 | 2001-07-02 | Arthur Jacques Kami Christiaan | DETERGENT COMPOSITIONS |
| ZA974222B (en) * | 1996-05-17 | 1998-12-28 | Procter & Gamble | Detergent composition |
| DE19626620A1 (en) * | 1996-07-03 | 1998-01-08 | Clariant Gmbh | Enzyme-containing detergent formulation |
| EP0934389B1 (en) * | 1996-10-18 | 2003-12-10 | The Procter & Gamble Company | Detergent compositions |
| TR199900851T2 (en) * | 1996-10-18 | 1999-07-21 | The Procter & Gamble Company | Detergent compositions. |
| AR017744A1 (en) * | 1999-02-08 | 2001-09-12 | Procter & Gamble | POLYMERIC GLYCOLS AND DIOLES FOR IMPROVED DETERGENT COMPOSITIONS FOR THE WASHING OF VAJILLA |
| JP5396707B2 (en) * | 2007-11-07 | 2014-01-22 | ライオンハイジーン株式会社 | Cleaning composition |
| EP2083067A1 (en) | 2008-01-25 | 2009-07-29 | Basf Aktiengesellschaft | Use of organic complexing agents and/or polymeric compounds containing carbonic acid groups in a liquid washing or cleaning agent compound |
| US20120324655A1 (en) | 2011-06-23 | 2012-12-27 | Nalini Chawla | Product for pre-treatment and laundering of stained fabric |
| JP6052777B2 (en) * | 2012-12-26 | 2016-12-27 | 花王株式会社 | Liquid detergent composition |
| JP7788825B2 (en) * | 2021-10-01 | 2025-12-19 | ライオン株式会社 | Washing Instructions |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2648304A1 (en) * | 1975-10-31 | 1977-05-05 | Procter & Gamble Europ | LIQUID DETERGENT |
| DE2857161A1 (en) * | 1977-06-29 | 1980-03-06 | Procter & Gamble | DETERGENT AND CLEANING AGENT |
| CH644394A5 (en) * | 1977-11-17 | 1984-07-31 | Procter & Gamble | GRAINY DETERGENT AND DETERGENT COMPOSITION. |
| GR70683B (en) * | 1979-02-27 | 1982-12-20 | Procter & Gamble | |
| EP0019315B1 (en) * | 1979-05-16 | 1983-05-25 | Procter & Gamble European Technical Center | Highly concentrated fatty acid containing liquid detergent compositions |
| DE3166434D1 (en) * | 1980-06-17 | 1984-11-08 | Procter & Gamble | Detergent composition containing low levels of amine oxides |
| US4394305A (en) * | 1981-03-17 | 1983-07-19 | The Procter & Gamble Company | Alpha-oxyalkylene amine oxide compounds useful in detergents |
| US4397776A (en) * | 1981-03-17 | 1983-08-09 | The Procter & Gamble Company | Liquid detergent compositions containing alpha-amine oxide surfactants |
-
1983
- 1983-05-16 AT AT83200688T patent/ATE22920T1/en not_active IP Right Cessation
- 1983-05-16 DE DE8383200688T patent/DE3366958D1/en not_active Expired
- 1983-05-16 EP EP83200688A patent/EP0095205B1/en not_active Expired
- 1983-05-17 GR GR71374A patent/GR78820B/el unknown
- 1983-05-20 CA CA000428642A patent/CA1208519A/en not_active Expired
- 1983-05-23 AU AU14888/83A patent/AU559791B2/en not_active Ceased
- 1983-05-23 FI FI831832A patent/FI73727C/en not_active IP Right Cessation
- 1983-05-23 MX MX197392A patent/MX162610A/en unknown
- 1983-05-23 IE IE1206/83A patent/IE55427B1/en not_active IP Right Cessation
- 1983-05-24 JP JP58090149A patent/JPS5925894A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| ATE22920T1 (en) | 1986-11-15 |
| MX162610A (en) | 1991-05-31 |
| EP0095205A1 (en) | 1983-11-30 |
| FI73727C (en) | 1987-11-09 |
| AU559791B2 (en) | 1987-03-19 |
| FI831832L (en) | 1983-11-25 |
| IE831206L (en) | 1983-11-24 |
| GR78820B (en) | 1984-10-02 |
| EP0095205B1 (en) | 1986-10-15 |
| FI831832A0 (en) | 1983-05-23 |
| JPH0477038B2 (en) | 1992-12-07 |
| JPS5925894A (en) | 1984-02-09 |
| CA1208519A (en) | 1986-07-29 |
| DE3366958D1 (en) | 1986-11-20 |
| AU1488883A (en) | 1983-12-01 |
| FI73727B (en) | 1987-07-31 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM4A | Patent lapsed |