WO2016009150A1 - Composition d'assouplissement des tissus comprenant un epaississant heur - Google Patents
Composition d'assouplissement des tissus comprenant un epaississant heur Download PDFInfo
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- WO2016009150A1 WO2016009150A1 PCT/FR2015/051946 FR2015051946W WO2016009150A1 WO 2016009150 A1 WO2016009150 A1 WO 2016009150A1 FR 2015051946 W FR2015051946 W FR 2015051946W WO 2016009150 A1 WO2016009150 A1 WO 2016009150A1
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- agent
- polyurethane
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- 239000000203 mixture Substances 0.000 title claims abstract description 87
- 239000004744 fabric Substances 0.000 title claims abstract description 52
- 239000002562 thickening agent Substances 0.000 title claims description 35
- 239000004814 polyurethane Substances 0.000 claims abstract description 97
- 229920002635 polyurethane Polymers 0.000 claims abstract description 95
- 150000001875 compounds Chemical class 0.000 claims abstract description 42
- 238000009833 condensation Methods 0.000 claims abstract description 37
- 230000005494 condensation Effects 0.000 claims abstract description 37
- -1 poly(alkylene glycol Chemical compound 0.000 claims abstract description 37
- 125000002091 cationic group Chemical group 0.000 claims abstract description 33
- 230000008719 thickening Effects 0.000 claims abstract description 33
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 30
- 239000004902 Softening Agent Substances 0.000 claims abstract description 24
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 18
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 18
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 18
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims abstract description 16
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 10
- 229920005862 polyol Polymers 0.000 claims abstract description 8
- 150000003077 polyols Chemical class 0.000 claims abstract description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 26
- 238000003860 storage Methods 0.000 claims description 17
- 239000000654 additive Substances 0.000 claims description 6
- 239000002518 antifoaming agent Substances 0.000 claims description 6
- 230000003115 biocidal effect Effects 0.000 claims description 6
- 239000003139 biocide Substances 0.000 claims description 6
- 230000000996 additive effect Effects 0.000 claims description 5
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- 239000007844 bleaching agent Substances 0.000 claims description 3
- 239000003086 colorant Substances 0.000 claims description 3
- 230000002255 enzymatic effect Effects 0.000 claims description 3
- 230000003287 optical effect Effects 0.000 claims description 3
- 239000004480 active ingredient Substances 0.000 claims description 2
- 239000003205 fragrance Substances 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 25
- 239000004094 surface-active agent Substances 0.000 description 18
- 238000012360 testing method Methods 0.000 description 13
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 11
- 238000009472 formulation Methods 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 230000002209 hydrophobic effect Effects 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 8
- 239000003760 tallow Substances 0.000 description 8
- 239000013065 commercial product Substances 0.000 description 7
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 229920001223 polyethylene glycol Polymers 0.000 description 7
- 239000000470 constituent Substances 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- 229920001515 polyalkylene glycol Polymers 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 239000003945 anionic surfactant Substances 0.000 description 5
- 239000013011 aqueous formulation Substances 0.000 description 5
- 239000003153 chemical reaction reagent Substances 0.000 description 5
- 238000010348 incorporation Methods 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 239000002736 nonionic surfactant Substances 0.000 description 5
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 150000001768 cations Chemical class 0.000 description 4
- 239000008393 encapsulating agent Substances 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 235000019482 Palm oil Nutrition 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
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- 150000001298 alcohols Chemical class 0.000 description 3
- 125000003342 alkenyl group Chemical group 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 239000002540 palm oil Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
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- 239000007787 solid Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- JWZZKOKVBUJMES-UHFFFAOYSA-N (+-)-Isoprenaline Chemical compound CC(C)NCC(O)C1=CC=C(O)C(O)=C1 JWZZKOKVBUJMES-UHFFFAOYSA-N 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- VZDIRINETBAVAV-UHFFFAOYSA-N 2,4-diisocyanato-1-methylcyclohexane Chemical compound CC1CCC(N=C=O)CC1N=C=O VZDIRINETBAVAV-UHFFFAOYSA-N 0.000 description 2
- GNRKVLMFBDYHJW-UHFFFAOYSA-N 2-(methylamino)ethanol;methyl hydrogen sulfate Chemical compound C[NH2+]CCO.COS([O-])(=O)=O GNRKVLMFBDYHJW-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- 125000006539 C12 alkyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical class OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-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
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000011149 active material Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 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 2
- 125000003827 glycol group Chemical group 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 238000004900 laundering Methods 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 230000003472 neutralizing effect Effects 0.000 description 2
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- 239000002304 perfume Substances 0.000 description 2
- 150000004965 peroxy acids Chemical class 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
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- 239000002994 raw material Substances 0.000 description 2
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- 229910052708 sodium Inorganic materials 0.000 description 2
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- 239000002904 solvent Substances 0.000 description 2
- 239000013638 trimer Substances 0.000 description 2
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 2
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 2
- 150000003673 urethanes Chemical class 0.000 description 2
- OHTRJOZKRSVAOX-UHFFFAOYSA-N 1,3-diisocyanato-2-methylcyclohexane Chemical compound CC1C(N=C=O)CCCC1N=C=O OHTRJOZKRSVAOX-UHFFFAOYSA-N 0.000 description 1
- OVBFMUAFNIIQAL-UHFFFAOYSA-N 1,4-diisocyanatobutane Chemical compound O=C=NCCCCN=C=O OVBFMUAFNIIQAL-UHFFFAOYSA-N 0.000 description 1
- CDMDQYCEEKCBGR-UHFFFAOYSA-N 1,4-diisocyanatocyclohexane Chemical compound O=C=NC1CCC(N=C=O)CC1 CDMDQYCEEKCBGR-UHFFFAOYSA-N 0.000 description 1
- ATOUXIOKEJWULN-UHFFFAOYSA-N 1,6-diisocyanato-2,2,4-trimethylhexane Chemical compound O=C=NCCC(C)CC(C)(C)CN=C=O ATOUXIOKEJWULN-UHFFFAOYSA-N 0.000 description 1
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
- PWVUXRBUUYZMKM-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCOCCO PWVUXRBUUYZMKM-UHFFFAOYSA-N 0.000 description 1
- FKOKUHFZNIUSLW-UHFFFAOYSA-N 2-Hydroxypropyl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(C)O FKOKUHFZNIUSLW-UHFFFAOYSA-N 0.000 description 1
- OSCJHTSDLYVCQC-UHFFFAOYSA-N 2-ethylhexyl 4-[[4-[4-(tert-butylcarbamoyl)anilino]-6-[4-(2-ethylhexoxycarbonyl)anilino]-1,3,5-triazin-2-yl]amino]benzoate Chemical compound C1=CC(C(=O)OCC(CC)CCCC)=CC=C1NC1=NC(NC=2C=CC(=CC=2)C(=O)NC(C)(C)C)=NC(NC=2C=CC(=CC=2)C(=O)OCC(CC)CCCC)=N1 OSCJHTSDLYVCQC-UHFFFAOYSA-N 0.000 description 1
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 1
- QEBLLSSGRQCVJI-UHFFFAOYSA-N 3-[2-hydroxyethyl(methyl)azaniumyl]propanoate Chemical compound OCCN(C)CCC(O)=O QEBLLSSGRQCVJI-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229920000858 Cyclodextrin Polymers 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- XTUVJUMINZSXGF-UHFFFAOYSA-N N-methylcyclohexylamine Chemical compound CNC1CCCCC1 XTUVJUMINZSXGF-UHFFFAOYSA-N 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- LNWBFIVSTXCJJG-UHFFFAOYSA-N [diisocyanato(phenyl)methyl]benzene Chemical compound C=1C=CC=CC=1C(N=C=O)(N=C=O)C1=CC=CC=C1 LNWBFIVSTXCJJG-UHFFFAOYSA-N 0.000 description 1
- 239000000159 acid neutralizing agent Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 235000001053 badasse Nutrition 0.000 description 1
- 230000031018 biological processes and functions Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000000828 canola oil Substances 0.000 description 1
- 235000019519 canola oil Nutrition 0.000 description 1
- 229920001525 carrageenan Polymers 0.000 description 1
- 235000010418 carrageenan Nutrition 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 description 1
- KIQKWYUGPPFMBV-UHFFFAOYSA-N diisocyanatomethane Chemical compound O=C=NCN=C=O KIQKWYUGPPFMBV-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 150000002169 ethanolamines 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
- 239000000835 fiber Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 244000056931 lavandin Species 0.000 description 1
- 235000009606 lavandin Nutrition 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 125000004043 oxo group Chemical group O=* 0.000 description 1
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical group O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229940113115 polyethylene glycol 200 Drugs 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
- 238000007614 solvation Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 150000005691 triesters Chemical class 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/001—Softening compositions
-
- C—CHEMISTRY; METALLURGY
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4833—Polyethers containing oxyethylene units
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4833—Polyethers containing oxyethylene units
- C08G18/4837—Polyethers containing oxyethylene units and other oxyalkylene units
- C08G18/485—Polyethers containing oxyethylene units and other oxyalkylene units containing mixed oxyethylene-oxypropylene or oxyethylene-higher oxyalkylene end groups
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/75—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic
- C08G18/751—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring
- C08G18/752—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group
- C08G18/753—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group
- C08G18/755—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group and at least one isocyanate or isothiocyanate group linked to a secondary carbon atom of the cycloaliphatic ring, e.g. isophorone diisocyanate
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- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
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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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0008—Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
- C11D17/003—Colloidal solutions, e.g. gels; Thixotropic solutions or pastes
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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
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/001—Softening compositions
- C11D3/0015—Softening compositions liquid
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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
- C11D3/26—Organic compounds containing nitrogen
- C11D3/30—Amines; Substituted amines ; Quaternized amines
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- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
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- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3726—Polyurethanes
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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
- C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
- C11D2111/10—Objects to be cleaned
- C11D2111/12—Soft surfaces, e.g. textile
Definitions
- the present invention relates to the technical field of fabric softening compositions.
- Such fabric softening compositions are, for example, intended to be used in the rinse cycle of a washing or laundering process.
- the softening compositions comprise a softening agent dispersed in an aqueous solution.
- a softening agent dispersed in an aqueous solution.
- cationic softening agents is described in particular in documents US 2013/0065813, US 2008/0051309, US 2004/0087470 and US 6,020,304.
- thickeners can be used to increase the viscosities of fabric softening compositions containing a softening cationic agent. It is possible, for example, to use thickeners of natural origin (for example gelatins, starches, carrageenans), natural cellulose-based thickeners also called cellulose ethers, of the HEC type or of the HMHEC type (Hydrophobically Modified HEC), acrylic thickeners or thickeners bearing urethane linkages.
- natural origin for example gelatins, starches, carrageenans
- natural cellulose-based thickeners also called cellulose ethers
- HEC type or of the HMHEC type Hydrophobically Modified HEC
- acrylic thickeners or thickeners bearing urethane linkages for example, to use thickeners of natural origin (for example gelatins, starches, carrageenans), natural cellulose-based thickeners also called cellulose ethers, of the HEC type or of the HMHEC type (Hydrophobically
- documents US 2009/0124533 and US 6,020,304 describe the use of thickeners resulting from the condensation of a polyalkylene glycol with an isocyanate compound having a hydrophobic chain end. More specifically, the document US 2009/0124533 describes the use of a thickener which is the product of the addition of an isocyanate compound with a polyalkylene glycol and which has at the end of the chain a saturated and unsaturated C14-C20 alkyl radical. ethoxylated. US 6,020,304, meanwhile, describes the use of a thickener having urethane linkages with C8-C24 chain ends, linear or branched, alkyl or alkenyl, non-ethoxylated.
- the thickening polyurethanes or HEURs result from the condensation between 3 constituents, namely: a poly (alkylene glycol) type compound, a polyisocyanate and a reagent which confers associativity of the alkyl, aryl or aryalkyl consisting of a hydrophobic end group.
- a poly (alkylene glycol) type compound e.g., a poly(alkylene glycol) type compound
- a polyisocyanate e.g., a poly(alkylene glycol) type compound
- a reagent which confers associativity of the alkyl, aryl or aryalkyl consisting of a hydrophobic end group.
- US 2009/0291876 discloses an aqueous laundry treatment composition comprising a cationic softening agent and a viscosity modifier which is a linear water-soluble polymer.
- a polymer described as particularly preferred in this document is a polyurethane having at the
- An object of the present invention is a fabric softening composition, comprising a cationic fabric softening agent and a HEUR type thickener, allowing better thickening than the thickeners described in the prior art.
- Another object of the present invention is the use of a special thickening polyurethane for thickening a softening composition containing a cationic fabric softening agent.
- HEUR is an acronym for "Hydrophobically modified Ethoxylated URethane”.
- the percentages expressed represent percentages by weight and are expressed relative to the total weight of the reference element.
- a polymer comprises 10% of a monomer or a reagent
- the polymer comprises 10% by weight of this monomer or reagent relative to the total weight of this monomer or reagent. polymer.
- the expression "at least one” designates one or more compound (s) (for example: one or more compound (s) of formula (I), one or more polyol (s), a or more polyisocyanate (s)), such as a mixture of 2 to 5 compounds.
- alkyl is meant a linear or branched C x H 2 X + 1 group, where x ranges from 1 to 30, preferably from 10 to 30, or even from 12 to 28.
- alkenyl is meant a linear or branched C y H 2 y -1 group , where y ranges from 1 to 30, preferably from 10 to 30, or even from 12 to 28.
- the polyurethanes of the present invention are thickeners particularly suited to fabric softening compositions.
- An object of the present invention relates to a thickener belonging to the category of HEUR (Hydrophobically modified Ethoxylated URethane). It is a polymer, associative and nonionic, thickener for fabric softening compositions.
- HEUR Hydrophilic Polymer
- the thickening polyurethanes or HEURs of the present invention result from the reaction between a poly (alkylene glycol) type compound, a polyisocyanate and a reagent which confers associativity and which consists of a hydrophobic end group.
- a poly (alkylene glycol) type compound e.g., polyethylene glycol
- a polyisocyanate e.g., polyethylene glycol
- reagent which confers associativity and which consists of a hydrophobic end group.
- the polyurethane thickener for fabric softening compositions results from the condensation:
- R is a carbon chain, saturated or unsaturated, linear or branched, having from 17 to 24 carbon atoms,
- [(EO) m - (OP) n - (OB) p] represents an alkoxylated chain consisting of alkoxylated units, divided into blocks, alternating or random, chosen from the ethoxylated units EO, the propoxylated units OP and the butoxylated units OB and
- n, p represent, independently of one another, 0 or an integer ranging between 1 and 30, the sum of m, n and p being between 20 and 30,
- At least one polyol for example at least one poly (alkylene glycol) and c) at least one polyisocyanate.
- polyurethanes are particularly suitable for thickening formulations for softening tissues, which furthermore comprises a cationic fabric softening agent.
- the polyurethane according to the present invention comprises as constituent a) at least one compound of formula (I).
- the compounds of formula (I) consist of a hydrophobic part, which is a saturated or unsaturated carbon chain, linear or branched, having from 17 to 24 carbon atoms. They also consist of a hydrophilic part, which is a polyalkoxylated chain having between 20 and 30 alkoxylated units.
- the polyurethane according to the present invention may comprise several compounds of formula (I) different.
- said thickening polyurethane results from the condensation of at least one compound of formula (I) in which R is a carbon chain having at least one linear or branched unsaturation having from 17 to 24 carbon atoms.
- said thickening polyurethane results from the condensation of at least one compound of formula (I) in which R is a carbon chain, saturated or unsaturated, linear or branched, having from 18 to 23 carbon atoms, for example from 19 to 22 carbon atoms.
- R is a carbon chain, saturated or unsaturated, linear or branched, having 18, 19, 20, 21, 22 or 23 carbon atoms.
- R is, preferably, a carbon chain having an odd number of carbon atoms.
- said thickening polyurethane results from the condensation of at least one compound of formula (I) in which R is a linear carbon chain having one or more unsaturation (s), having from 17 to 24 carbon atoms.
- said thickening polyurethane results from the condensation of at least one compound of formula (I) in which R is a linear or branched saturated carbon chain having from 17 to 24 carbon atoms.
- the compounds of formula (I) also comprise a polyalkoxylated chain consisting of at least 20 alkoxylated units.
- the compounds of formula (I) contain a polyalkoxylated chain consisting of at most 30 alkoxylated units. According to one embodiment of the present invention, in formula (I) below:
- n represents an integer ranging between 1 and 30 (different from 0) and
- n and p represent, independently of one another, 0 or an integer ranging between 1 and 29,
- n and n represent an integer varying between 1 and 30 (different from 0) and p is equal to 0,
- n and p are 0 and
- n represents an integer ranging between 20 and 30, for example between 21 and 29 or for example equal to 25.
- said alkoxylated chain of the compound of formula (I) consists exclusively of ethoxylated units OE.
- said thickening polyurethane results from the condensation of at least one compound of formula (I) in which n and p are zero and m represents an integer ranging between 20 and 30.
- said thickening polyurethane results from the condensation of at least one compound of formula (I) in which n and p are zero and m represents an integer ranging between 25 and 30.
- the polyurethane comprises as component b) at least one polyol which may be a poly (alkylene glycol).
- poly (alkylene glycol) is meant a polymer of an alkylene glycol derived from an olefinic oxide.
- the polyalkylene glycol chains of component b) according to the present invention may, for example, contain a proportion of ethyleneoxy groups, a proportion of propyleneoxy groups and / or a proportion of butyleneoxy groups.
- the polyalkylene glycol chains according to the present invention may, for example, comprise a major proportion of ethyleneoxy groups in combination with a minor proportion of propyleneoxy groups.
- alkylene glycol polymers include: polyalkylene glycols having an average molecular weight of 1000 g / mol, 4000 g / mol, 6000 g / mol and 10,000 g / mol; polyethylene polypropylenes glycols having a percentage of ethylene oxide of between 20% and 80% by weight and a percentage of propylene oxide of between 20% and 80% by weight.
- the polyurethanes result from the condensation in particular of a poly (alkylene glycol) which comprises more than 80% by weight of ethylene oxide.
- the polyurethanes result from the condensation in particular of a poly (alkylene glycol) which is poly (ethylene glycol).
- a poly (ethylene glycol) which is poly (ethylene glycol).
- It may be, for example, a poly (ethylene glycol) whose molecular mass varies between 2,000 g / mol and 20,000 g / mol, for example between 8,000 g / mol and 15,000 g / mol ( terminals included).
- poly (ethylene glycol) (or PEG) with a molecular mass ranging from 10,000 g / mol to 12,000 g / mol (inclusive) or from a molecular weight of between 5,000 g / mol mol and 7000 g / mol (inclusive).
- poly (ethylene glycol) (or PEG) having more than 180 units of EO, for example 181 or more, or that having less than 180 EO units, for example 179 or less.
- the polyurethane according to the present invention may comprise several different polyalkylene glycols.
- the polyurethane comprises as component c) at least one polyisocyanate.
- the polyurethanes result from the condensation, in particular of a polyisocyanate which is chosen from the group consisting of toluene diisocyanate, toluene diisocyanate dimers, toluene diisocyanate trimers and 1,4-butane diisocyanate.
- the polyurethanes result from the condensation of at least one polyisocyanate which is isophorone diisocyanate (IPDI). According to another aspect of the present invention, the polyurethanes result from the condensation of at least one polyisocyanate selected from the group mentioned above with the exception of isophorone diisocyanate (IPDI).
- the polyurethane thickener for fabric softening compositions results from the condensation of: a) an alcohol-type compound, as described above,
- said thickening polyurethane results from the condensation of:
- said thickening polyurethane results from the condensation of:
- An object of the present invention also relates to a process for preparing a polyurethane as described above, said process consisting of a condensation of its various constituents. Formulation of the thickener HEUR
- the polyurethane according to the invention which results from the reaction of at least 3 constituents mentioned above, can be in different forms (solid or liquid).
- the powder form may be preferred by the formulator for incorporation into a given formulation or because of certain constraints (equipment available, volumes to be prepared).
- a polyurethane in liquid form, in particular for better dispersibility when added to aqueous systems and a shorter dissolution time.
- Most commercial associative thickeners are now sold in liquid form.
- the polyurethane according to the invention can also be formulated or co-formulated with other constituents or components, this independently of the final composition for softening the tissues.
- the polyurethane according to the invention can be formulated in water.
- said aqueous formulation according to the invention consists of:
- said aqueous formulation according to the invention consists of:
- the polyurethane according to the invention may be co-formulated in water, in the presence of at least one surfactant.
- This surfactant makes it possible to formulate the thickener in the form of a less viscous liquid aqueous solution which can thus be more easily implemented by the formulator.
- said aqueous formulation comprises a polyurethane, as described above, as well as water and a surfactant.
- surfactant or “surfactant” is meant a molecule or a polymer consisting of at least one hydrophilic part and at least one hydrophobic part.
- the surfactant used in the context of the present invention may be of a different nature, for example it may be anionic or nonionic.
- This surfactant may be selected from ionic surfactant classes (in this case preferably anionic), and / or nonionic and / or mixed (comprising in the same molecule a nonionic and anionic structure).
- the preferred surfactant is composed of at least one surfactant selected from the class of nonionic surfactant, optionally in the presence of an anionic surfactant.
- anionic surfactants mention may be made of sodium, lithium, potassium, ammonium or magnesium salts derived from alkyl ether sulphates with C6 to C12 alkyl, in a linear, iso, oxo, geminate, cyclic or aromatic configuration, or C12 alkyl sulfates, alkyl phosphate esters or dialkyl sulfosuccinates.
- the anionic surfactants are preferably used with at least one nonionic surfactant.
- mixed surfactants include alkoxylated alkyl phenol sulfonates.
- the nonionic surfactants can be used alone or in combination with an anionic surfactant.
- suitable nonionic surfactants include: ethoxylated C4-C18 alcohols (2 to 15 EO), Ethoxylated C4-C18 guerbet (2-40 EO), ethoxylated (2-40E) C10-C18 monobranched alcohols, C18 sorbitol esters, ethoxylated sorbitol esters (2-20 EO units), ethoxylated C4-C18 acids (less than 15 EO), ethoxylated castor oil (30 to 40 EO), ethoxylated hydrogenated castor oil (7 to 60 EO), esters such as, for example, palmitate; glycerol, glycerol stearate, ethylene glycol stearate, diethylene glycol stearate, propylene glycol stearate, polyethylene
- the polyurethane of the present invention is formulated in the presence of at least one nonionic surfactant, optionally combined with at least one anionic surfactant, with a total content in weight ranging from 5% to 30% by weight. for example from 8% to 20% by weight or from 10% to 17% by weight.
- the weight ratio between the two surfactants may, for example, vary between 25/75 and 75/25.
- the polyurethane of the present invention is formulated in the presence of more than two surfactants, for example three or four.
- said aqueous formulation according to the invention consists of:
- the polyurethane according to the invention may be formulated in a solvent miscible with water.
- the main reason for adding an organic co-solvent is to lower the viscosity of this polyurethane in water, to facilitate handling.
- the polyurethane is, for example, formulated with one or more polar solvent (s) belonging in particular to the group consisting of water, methanol, ethanol, propanol, isopropanol, butanols, acetone. , tetrahydrofuran or their mixtures.
- a water-miscible organic solvent is diethylene glycol monobutyl ether (also known as Butyl Carbitol TM) or ethylene or propylene glycol.
- the viscosity of the polyurethane as it is before incorporation into a fabric softening composition is preferably less than 10,000 mPa.s at 25 ° C and 100 rpm, so that it is easier to pour from the storage container and more rapidly incorporated into the composition to be thickened at room temperature.
- the water-miscible solvent chosen for such commercial compositions has, to date, exclusively been an organic solvent.
- the HEUR thickener formulation further comprises at least one additive selected from the group consisting of a biocide, a pH regulator, an antifoam agent, an encapsulant and mixtures thereof.
- Biocide means a chemical substance intended to destroy, repel or render harmless harmful organisms, to prevent their action or to combat them in any other way, by chemical or biological action.
- pH regulating agent an agent capable of significantly varying the pH of the formulation.
- the pH regulating agent can increase the pH, which is the case for bases such as NaOH.
- the pH regulating agent can reduce the pH, which is the case of acids.
- one or more neutralization agent (s) having a monovalent neutralizing function and / or a divalent or polyvalent neutralizing function such as, for example:
- alkaline cations in particular sodium, potassium, lithium, ammonium or primary, secondary or tertiary aliphatic and / or cyclic amines
- alkaline cations in particular sodium, potassium, lithium, ammonium or primary, secondary or tertiary aliphatic and / or cyclic amines
- stearylamine ethanolamines (mono-, di-, triethanolamine), mono and diethylamine, cyclohexylamine, methylcyclohexylamine and
- divalent alkaline earth cations in particular magnesium, calcium, zinc, as well as by trivalent cations, in particular aluminum, or alternatively by some higher valence cations.
- aqueous formulation consists of:
- At least one other additive selected from the group consisting of a biocide, a pH regulator, an antifoaming agent, an encapsulant and mixtures thereof, preferably 0.5% to 4% by weight,
- the present invention also relates to a fabric softening composition
- a fabric softening composition comprising a thickening polyurethane according to the invention, as described above, as well as a cationic fabric softening agent.
- the cationic conferring softening agent is dispersed within the aqueous composition.
- Such fabric softening compositions are, for example, intended to be used in the rinse cycle of a washing or laundering process.
- the softening composition according to the invention facilitates the dosage during use.
- consumers generally consider that the effectiveness of the compositions is related to their viscosity.
- the softening composition according to the invention comprises a thickener.
- the viscosity of said fabric softening composition is greater than 300 mPa.s, for example greater than 400 mPa.s or 500 mPa.s.
- the present invention also relates to fabric softening compositions that disperse readily in water at the time of use, particularly in washing machines equipped with automatic dispensing mechanisms.
- the fabric softening compositions have a thick sis / stable viscosity over time for a period of at least 7 days, preferably for a period of at least 14 days.
- stable is meant that the viscosity as measured with a Brookfield type RVT viscometer, after 7 days of storage (storage temperature: 25 ° C.), preferably after 14 days of storage, in the unstirred bottle, at a temperature of 25 ° C at the speed of rotation of 20 rpm is at least equal to 50% of the viscosity measured according to the same protocol after 24 hours of storage in the unstirred vial, at a temperature of 25 ° C. .
- the fabric softening composition comprising:
- R is a carbon chain, saturated or unsaturated, linear or branched, having
- [(EO) m - (OP) n - (OB) p] represents an alkoxylated chain consisting of alkoxylated units, divided into blocks, alternating or random, chosen from the ethoxylated units EO, the propoxylated units OP and the butoxylated units OB and
- n, p represent, independently of one another, 0 or an integer ranging between 1 and 30, the sum of m, n and p being between 20 and 30,
- At least one polyol for example at least one poly (alkylene glycol) and c) at least one polyisocyanate,
- a rheological profile such as: its viscosity ⁇ , as measured with a Brookfield type RVT viscometer, after 24 hours of storage (at 25 ° C.), in the unstirred bottle, at a temperature of 25 ° C. at a speed of rotation of 20 rpm is greater than 300 mPa.s, for example greater than 400 mPa.s or 500 mPa.s and
- ⁇ 2 its viscosity ⁇ 2 , as measured with a Brookfield type RVT viscometer, after 7 days of storage (at 25 ° C.), for example after 14 days of storage, in the unstirred flask, at a temperature of 25 ° C. to the speed of rotation of 20 revolutions per minute is greater than 50% of the value of ⁇ , for example greater than 60% or 70% of the value of ⁇ 1 .
- the cationic fabric softening agent is chosen so as to bring softness and swelling to the tissues treated during rinsing, after leaching. It is also likely to provide antistatic properties. Without being bound by the following theory concerning the mechanism of action of the cationic fabric softening agents, it is probable that the fixation, via the cationic unit, of fatty chains on the surface of the fibers lubricates them and allows them to to move relative to each other, thus reducing the impression of stiffness associated with an untreated linen.
- the cationic fabric softening agent can in particular be a compound comprising an N + cationic nitrogen atom, at least one fatty chain, for example a carbon chain of 4 to 36 atoms, and at least one ester function.
- the fatty chain may include atoms other than carbon atoms.
- it may comprise Si silica atoms.
- the N + cationic nitrogen atom may be linked to the fatty chains through the ester functions, for example through:
- quaternary ammonium compounds containing an ester can be used in the context of the present invention including quaternary triester ammonium compounds (TEQ) and quaternary ammonium diester compounds (DEQ). These compounds may also comprise a mixture of mono- (I), di- (II) and tri- (III) esters.
- said cationic fabric softening agent is a triester quaternary ammonium compound (TEQ) and / or a diester quaternary ammonium compound (DEQ).
- Esterquat-type compounds are commercially available. They are sometimes called, in an equivalent manner, cationic surfactants.
- the compounds of esterquat type according to the invention may, for example, consist of two or three ester radicals substituted with alkyl or alkenyl groups, according to the definition given above.
- the cationic fabric softening agent is, for example, chosen, without limitation, from the list of products below:
- Stepantex TM DC 90 (Stepan company), origin: rapeseed oil,
- Stepantex TM VA or Stepantex TM VL 90A (Stepan company), origin: partially hydrogenated tallow
- Stepantex TM VR 90 (Stepan company), origin: tallow, Di (Tallowamidoethyl) hydroxyethylmethylammonium methylsulphate (Incrosoft T90, Croda company), origin: tallow,
- Tallowoylethyl Hydroxyethyl Hydroxyethylmonium Methosulfate and Ditallowoylethyl Hydroxyethylmonium Methosulfate (Britesoft TM EQ 90, Chemelco Company),
- Tetranyl L1 / 90S TM or Tetranyl TM ATI (Kao company), origin: animal tallow,
- Tetranyl L6 / 90 TM (Kao company), origin: palm oil
- the aqueous composition further comprises at least one additive selected from the group consisting of a fragrance, a biocide, a pH regulator, an antifoam agent, a coloring agent, an agent antistatic agent, an opacifying agent, a bleaching agent (for example a peracid), an enzymatic agent and an optical brightener.
- a fragrance for example a fragrance, a biocide, a pH regulator, an antifoam agent, a coloring agent, an agent antistatic agent, an opacifying agent, a bleaching agent (for example a peracid), an enzymatic agent and an optical brightener.
- a fragrance selected from the group consisting of a fragrance, a biocide, a pH regulator, an antifoam agent, a coloring agent, an agent antistatic agent, an opacifying agent, a bleaching agent (for example a peracid), an enzymatic agent and an optical brightener.
- a bleaching agent for example a peracid
- the aqueous composition comprises from 0.02% to 5% by weight of active material of said polyurethane.
- the aqueous composition comprises from 0.05% to 2% by weight of active material of said polyurethane.
- the aqueous composition comprises
- the softening composition is prepared according to conventional methods, known to those skilled in the art.
- the cationic fabric softening agent is generally in a solid form at room temperature, so it is necessary to melt it before incorporating it into an aqueous composition. Thus, this agent is heated to a temperature at least greater than its melting temperature.
- the cationic fabric softening agent is heated at a temperature of between 45 ° C. and 70 ° C., for example between 50 ° C. and 65 ° C., before being incorporated into the remainder of the formulation. .
- the cationic agent for softening the tissues in liquid form, in the molten state is incorporated in a volume of water, for example demineralised, preheated to a minimum. temperature at least higher than the melting temperature of the cationic fabric softening agent.
- said volume of water, for example demineralised is heated to a temperature greater than 45 ° C., for example greater than 50 ° C., for example 70 ° C. C ⁇ 2 ° C.
- the incorporation of the cationic agent in liquid form, in the molten state, into the said volume of water is preferably stirred.
- the solution After incorporation of the fabric softening agent into the determined amount of water, the solution is allowed to cool to a temperature below the melting temperature of the cationic fabric softening agent.
- the solution is allowed to cool to a temperature below 40 ° C, for example below 35 ° C, for example a temperature of 30 ° C + 2 ° C.
- the additive (s) selected from the group consisting of a perfume, a biocide, a pH regulator, an antifoaming agent, a coloring agent, an antistatic agent, a opacifying agent, a bleaching agent (for example a peracid), an enzymatic agent and an optical brightener.
- the polyurethane thickener according to the present invention is added as described above. The addition of the polyurethane can be done with stirring or using any means allowing homogeneous incorporation of said polyurethane in the formulation.
- said thickening polyurethane resulting from condensation is:
- R is a carbon chain, saturated or unsaturated, linear or branched, having from 17 to 24 carbon atoms,
- [(EO) m - (OP) n - (OB) p] represents an alkoxylated chain consisting of alkoxylated units, divided into blocks, alternating or random, chosen from the ethoxylated units EO, the propoxylated units OP and the butoxylated units OB and
- n, p represent, independently of one another, 0 or an integer ranging between 1 and 30, the sum of m, n and p being between 20 and 30,
- At least one polyol for example at least one poly (alkylene glycol) and c) at least one polyisocyanate,
- a softening composition containing a cationic fabric softening agent is used to thicken a softening composition containing a cationic fabric softening agent.
- Said polyurethane may in particular be used to thicken a fabric softening composition at a viscosity ⁇ , as measured with a Brookfield viscometer type RVT, after 24 hours of storage at 25 ° C., in the unstirred bottle, at a temperature of 25 ° C at the speed of rotation of 20 rpm, greater than 300 mPa.s, for example greater than 400 mPa.s or 500 mPa.s.
- the viscosity of the fabric softening composition is dependent on the concentration of polyurethane thickeners.
- the formulator knows how to adapt this concentration to obtain the expected viscosity.
- Thickeners according to the invention allow equal doses to obtain a thick sis significantly improved compared to the polyurethane thickeners of the prior art.
- Said polyurethane may in particular be used to thicken a fabric softening composition to:
- a viscosity ⁇ 2 as measured with a Brookfield viscometer type RVT, after 7 days of storage, for example after 14 days of storage, in the unstirred bottle, at a temperature of 25 ° C. at a rotation speed of 20 ° C. revolutions per minute, greater than 50% of the value of ⁇ , for example greater than 60% or 70% of the value of ⁇ 1 .
- This example illustrates the use of thickening polyurethanes according to the invention in a fabric softening composition comprising a cationic esterquat agent. All raw materials are commercially available.
- Stepan at 60 ° C. 944.4 g of demineralized water are heated to 70 ° C. The water is stirred and the cationic agent is poured into the hot water. The mixture is allowed to cool to 30 ° C with continuous stirring.
- tests 1-4 and 1-5) are implemented polyurethanes according to the invention (tests 1-4 and 1-5), using a compound of formula (I).
- this example also illustrates polyurethanes outside the invention (tests 1-1, 1-2, 1-3 and 1-6).
- Said polyurethane results from the condensation of, expressed in% by weight relative to the total weight of the polyurethane:
- Said polyurethane results from the condensation of, expressed in% by weight relative to the total weight of the polyurethane:
- R is a C20: 0 chain, branched to 20 carbon atoms
- Said polyurethane results from the condensation of, expressed in% by weight relative to the total weight of the polyurethane:
- R is a linear C12: 0 chain with 12 carbon atoms
- IPDI isophorone diisocyanate
- Said polyurethane results from the condensation of, expressed in% by weight relative to the total weight of the polyurethane:
- R is a Cl chain 8: 1, linear to 18 carbon atoms having unsaturation,
- IPDI isophorone diisocyanate
- Said polyurethane results from the condensation of, expressed in% by weight relative to the total weight of the polyurethane:
- R is a C22: 0 chain, linear with 22 carbon atoms
- IPDI isophorone diisocyanate
- the exemplified polyurethane results from the condensation of two different alcohols of formula (I). More specifically, said polyurethane results from the condensation of, expressed in% by weight relative to the total weight of the polyurethane:
- R is a linear C12: 0 chain with 12 carbon atoms
- R is a C32: 0 chain, branched to 32 carbon atoms
- IPDI isophorone diisocyanate
- Polyurethanes are formulated in water in the presence of a surfactant which is Mergital® D8. PU / surfactant / water ratios are 17.5 / 9.5 / 73.
- the thickening polyurethanes according to the invention allow a stable thickening at 7 days and at 14 days: the ratio ⁇ 2 / ⁇ () is greater than 50% for all the tests carried out with a thickening polyurethane meeting the criteria of the present invention, which is not the case for the thickeners outside the invention.
- Example 2
- This example illustrates the use of a thickening polyurethane according to the invention in a fabric softening composition, comprising a quat cationic agent. All raw materials are commercially available.
- Test 2-1 (according to the invention)
- Said polyurethane results from the condensation of, expressed in% by weight relative to the total weight of the polyurethane:
- R is a C22: 0 chain, linear with 22 carbon atoms
- IPDI isophorone diisocyanate
- Polyurethane is formulated in water in the presence of a surfactant which is Mergital® D8.
- PU / surfactant / water ratios are 17.5 / 9.5 / 73.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Dispersion Chemistry (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Polyurethanes Or Polyureas (AREA)
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA2951115A CA2951115A1 (fr) | 2014-07-18 | 2015-07-16 | Composition d'assouplissement des tissus comprenant un epaississant heur |
CN201580031070.6A CN106459845A (zh) | 2014-07-18 | 2015-07-16 | 含有heur增稠剂的织物软化组合物 |
MX2016017050A MX2016017050A (es) | 2014-07-18 | 2015-07-16 | Composicion suavizante de telas que comprende un espesante heur. |
EP15756197.8A EP3169764A1 (fr) | 2014-07-18 | 2015-07-16 | Composition d'assouplissement des tissus comprenant un epaississant heur |
US15/315,259 US20170198238A1 (en) | 2014-07-18 | 2015-07-16 | Fabric-softening composition comprising an heur thickener |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR1456934 | 2014-07-18 | ||
FR1456934A FR3023846B1 (fr) | 2014-07-18 | 2014-07-18 | Composition d'assouplissement des tissus comprenant un epaississant heur. |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2016009150A1 true WO2016009150A1 (fr) | 2016-01-21 |
Family
ID=51659878
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/FR2015/051946 WO2016009150A1 (fr) | 2014-07-18 | 2015-07-16 | Composition d'assouplissement des tissus comprenant un epaississant heur |
Country Status (7)
Country | Link |
---|---|
US (1) | US20170198238A1 (fr) |
EP (1) | EP3169764A1 (fr) |
CN (1) | CN106459845A (fr) |
CA (1) | CA2951115A1 (fr) |
FR (1) | FR3023846B1 (fr) |
MX (1) | MX2016017050A (fr) |
WO (1) | WO2016009150A1 (fr) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR3023845B1 (fr) * | 2014-07-18 | 2018-01-05 | Coatex Sas | Composition d'assouplissement des tissus comprenant un epaississant heur. |
FR3075206B1 (fr) * | 2017-12-19 | 2020-07-24 | Coatex Sas | Agent epaississant et composition assouplissante |
WO2020212779A1 (fr) | 2019-04-16 | 2020-10-22 | 3M Innovative Properties Company | Article abrasif et son procédé de fabrication |
US20230059614A1 (en) | 2020-02-10 | 2023-02-23 | 3M Innovative Properties Company | Coated abrasive article and method of making the same |
EP4188646A1 (fr) | 2020-07-28 | 2023-06-07 | 3M Innovative Properties Company | Article abrasif revêtu et procédé de fabrication d'un tel article |
EP4225532B1 (fr) | 2020-10-08 | 2025-02-26 | 3M Innovative Properties Company | Article abrasif revêtu et procédé de fabrication de celui-ci |
WO2022074601A1 (fr) | 2020-10-09 | 2022-04-14 | 3M Innovative Properties Company | Article abrasif et son procédé de fabrication |
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US6001797A (en) * | 1998-07-20 | 1999-12-14 | Colgate-Palmolive Co. | Liquid fabric softening compositions containing a fatty alcohol ethoxylate diurethane polymer as a thickener |
US6020304A (en) | 1996-04-01 | 2000-02-01 | The Procter & Gamble Company | Fabric softener compositions |
EP1013264A1 (fr) * | 1998-12-17 | 2000-06-28 | Shiseido Company Limited | Composition cosmétique |
US20040087470A1 (en) | 2002-11-01 | 2004-05-06 | Colgate-Palmolive Company | Aqueous composition comprising oligomeric esterquats |
EP1849855A1 (fr) * | 2006-04-27 | 2007-10-31 | Degussa GmbH | Compositions assouplissantes thixotropiques |
US20070293625A1 (en) * | 2006-06-14 | 2007-12-20 | Borchers Gmbh | New polyurethanes and their use for thickening aqueous systems |
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US20090291876A1 (en) | 2005-06-14 | 2009-11-26 | Paul William Blanco | Fabric Softening Composition |
US20130065813A1 (en) | 2011-09-13 | 2013-03-14 | Juan Felipe Miravet Celades | Fluid fabric enhancer compositions |
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JPS5277292A (en) * | 1975-12-22 | 1977-06-29 | Toray Industries | Production of fiber structure |
JPS5634752A (en) * | 1979-08-29 | 1981-04-07 | Tokai Seiyu Kogyo Kk | Production of fiber-finishing agent |
JP2625374B2 (ja) * | 1993-12-16 | 1997-07-02 | グンゼ株式会社 | 耐久柔軟仕上剤 |
FR2732031B1 (fr) * | 1995-03-23 | 1997-04-30 | Coatex Sa | Utilisation d'agents amphoteres comme modificateurs de phases lamellaires de compositions detergentes ou cosmetiques liquides ou pateuses |
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FR2948374B1 (fr) * | 2009-07-23 | 2012-06-08 | Cray Valley Sa | Dispersion aqueuse de polymere autoreticulable, a base de particules de polymere structurees en coeur dur et ecorce molle et compositions de revetements ou de traitement |
US20120082629A1 (en) * | 2010-09-01 | 2012-04-05 | Basf Se | Associative Thickeners For Aqueous Preparations |
FR3000085B1 (fr) * | 2012-12-20 | 2016-06-10 | Coatex Sas | Agent polymerique pour obtenir une composition aqueuse stable comprenant des particules en suspension |
FR3000086B1 (fr) * | 2012-12-20 | 2014-12-26 | Coatex Sas | Agent pour obtenir une composition aqueuse stable comprenant des particules en suspension |
FR3023845B1 (fr) * | 2014-07-18 | 2018-01-05 | Coatex Sas | Composition d'assouplissement des tissus comprenant un epaississant heur. |
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2014
- 2014-07-18 FR FR1456934A patent/FR3023846B1/fr not_active Expired - Fee Related
-
2015
- 2015-07-16 US US15/315,259 patent/US20170198238A1/en not_active Abandoned
- 2015-07-16 CN CN201580031070.6A patent/CN106459845A/zh active Pending
- 2015-07-16 EP EP15756197.8A patent/EP3169764A1/fr not_active Withdrawn
- 2015-07-16 WO PCT/FR2015/051946 patent/WO2016009150A1/fr active Application Filing
- 2015-07-16 CA CA2951115A patent/CA2951115A1/fr not_active Abandoned
- 2015-07-16 MX MX2016017050A patent/MX2016017050A/es unknown
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US6020304A (en) | 1996-04-01 | 2000-02-01 | The Procter & Gamble Company | Fabric softener compositions |
US6001797A (en) * | 1998-07-20 | 1999-12-14 | Colgate-Palmolive Co. | Liquid fabric softening compositions containing a fatty alcohol ethoxylate diurethane polymer as a thickener |
EP1013264A1 (fr) * | 1998-12-17 | 2000-06-28 | Shiseido Company Limited | Composition cosmétique |
US20040087470A1 (en) | 2002-11-01 | 2004-05-06 | Colgate-Palmolive Company | Aqueous composition comprising oligomeric esterquats |
US20080051309A1 (en) | 2004-12-27 | 2008-02-28 | Bin Lin | Liquid Laundry Detergent Containing Fabric Condictioners |
US20090291876A1 (en) | 2005-06-14 | 2009-11-26 | Paul William Blanco | Fabric Softening Composition |
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Also Published As
Publication number | Publication date |
---|---|
EP3169764A1 (fr) | 2017-05-24 |
CN106459845A (zh) | 2017-02-22 |
US20170198238A1 (en) | 2017-07-13 |
MX2016017050A (es) | 2017-05-12 |
FR3023846B1 (fr) | 2017-12-22 |
CA2951115A1 (fr) | 2016-01-21 |
FR3023846A1 (fr) | 2016-01-22 |
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