CN1120836A - 具有改进的冷水可分散性的脂肪酸酰胺 - Google Patents
具有改进的冷水可分散性的脂肪酸酰胺 Download PDFInfo
- Publication number
- CN1120836A CN1120836A CN94191762A CN94191762A CN1120836A CN 1120836 A CN1120836 A CN 1120836A CN 94191762 A CN94191762 A CN 94191762A CN 94191762 A CN94191762 A CN 94191762A CN 1120836 A CN1120836 A CN 1120836A
- Authority
- CN
- China
- Prior art keywords
- acid
- numerical value
- formula
- group
- carbon atoms
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 235000014113 dietary fatty acids Nutrition 0.000 title claims abstract description 25
- 239000000194 fatty acid Substances 0.000 title claims abstract description 25
- 229930195729 fatty acid Natural products 0.000 title claims abstract description 25
- 150000004665 fatty acids Chemical class 0.000 title claims abstract description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 16
- 239000002253 acid Substances 0.000 claims abstract description 25
- 239000006185 dispersion Substances 0.000 claims abstract description 15
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 13
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 13
- 150000001412 amines Chemical class 0.000 claims abstract description 12
- 125000003277 amino group Chemical group 0.000 claims abstract description 8
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 7
- 150000002148 esters Chemical class 0.000 claims abstract description 7
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 5
- 150000002632 lipids Chemical class 0.000 claims description 14
- -1 hydroxyethyl groups Chemical group 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 12
- 238000002360 preparation method Methods 0.000 claims description 11
- 239000004753 textile Substances 0.000 claims description 11
- 239000001257 hydrogen Substances 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 9
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims description 6
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 6
- 238000009833 condensation Methods 0.000 claims description 5
- 230000005494 condensation Effects 0.000 claims description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
- 125000002252 acyl group Chemical group 0.000 claims description 4
- 125000001931 aliphatic group Chemical group 0.000 claims description 3
- 239000004310 lactic acid Substances 0.000 claims description 3
- 235000014655 lactic acid Nutrition 0.000 claims description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
- 238000006068 polycondensation reaction Methods 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 150000002193 fatty amides Chemical class 0.000 claims 1
- 238000012545 processing Methods 0.000 abstract description 7
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- 150000001408 amides Chemical class 0.000 abstract 1
- 230000003472 neutralizing effect Effects 0.000 abstract 1
- 239000004744 fabric Substances 0.000 description 17
- 239000000047 product Substances 0.000 description 14
- 239000007859 condensation product Substances 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 239000003760 tallow Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- 235000021355 Stearic acid Nutrition 0.000 description 3
- 238000006482 condensation reaction Methods 0.000 description 3
- 150000002191 fatty alcohols Chemical class 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 3
- 239000008117 stearic acid Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-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
- 244000060011 Cocos nucifera Species 0.000 description 2
- 235000013162 Cocos nucifera Nutrition 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- DLRVVLDZNNYCBX-UHFFFAOYSA-N Polydextrose Polymers OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(O)O1 DLRVVLDZNNYCBX-UHFFFAOYSA-N 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- ZQPPMHVWECSIRJ-MDZDMXLPSA-N elaidic acid Chemical compound CCCCCCCC\C=C\CCCCCCCC(O)=O ZQPPMHVWECSIRJ-MDZDMXLPSA-N 0.000 description 2
- HNRMPXKDFBEGFZ-UHFFFAOYSA-N ethyl trimethyl methane Natural products CCC(C)(C)C HNRMPXKDFBEGFZ-UHFFFAOYSA-N 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- VKOBVWXKNCXXDE-UHFFFAOYSA-N icosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCC(O)=O VKOBVWXKNCXXDE-UHFFFAOYSA-N 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229940055577 oleyl alcohol Drugs 0.000 description 2
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 229940059574 pentaerithrityl Drugs 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Substances CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000600 sorbitol Substances 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- 238000004448 titration Methods 0.000 description 2
- CUXYLFPMQMFGPL-UHFFFAOYSA-N (9Z,11E,13E)-9,11,13-Octadecatrienoic acid Natural products CCCCC=CC=CC=CCCCCCCCC(O)=O CUXYLFPMQMFGPL-UHFFFAOYSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- UQHRGLKDNKYFBB-UHFFFAOYSA-N 1,2-diaminobutan-2-ol Chemical class CCC(N)(O)CN UQHRGLKDNKYFBB-UHFFFAOYSA-N 0.000 description 1
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- PZDTYFSTRBOWET-UHFFFAOYSA-N 3-[2-(2-aminoethylamino)ethylamino]propan-1-ol Chemical compound NCCNCCNCCCO PZDTYFSTRBOWET-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 240000007087 Apium graveolens Species 0.000 description 1
- 235000015849 Apium graveolens Dulce Group Nutrition 0.000 description 1
- 235000010591 Appio Nutrition 0.000 description 1
- DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 description 1
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- URXZXNYJPAJJOQ-UHFFFAOYSA-N Erucic acid Natural products CCCCCCC=CCCCCCCCCCCCC(O)=O URXZXNYJPAJJOQ-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 208000007976 Ketosis Diseases 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- LPQOADBMXVRBNX-UHFFFAOYSA-N ac1ldcw0 Chemical compound Cl.C1CN(C)CCN1C1=C(F)C=C2C(=O)C(C(O)=O)=CN3CCSC1=C32 LPQOADBMXVRBNX-UHFFFAOYSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001323 aldoses Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- CUXYLFPMQMFGPL-SUTYWZMXSA-N all-trans-octadeca-9,11,13-trienoic acid Chemical compound CCCC\C=C\C=C\C=C\CCCCCCCC(O)=O CUXYLFPMQMFGPL-SUTYWZMXSA-N 0.000 description 1
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 1
- LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- MMCOUVMKNAHQOY-UHFFFAOYSA-N carbonoperoxoic acid Chemical compound OOC(O)=O MMCOUVMKNAHQOY-UHFFFAOYSA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- GLUUGHFHXGJENI-UHFFFAOYSA-N diethylenediamine Natural products C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- DPUOLQHDNGRHBS-KTKRTIGZSA-N erucic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 description 1
- LONYOMRPNGXPGP-UHFFFAOYSA-N ethene-1,1-diol Chemical group [CH2][C](O)O LONYOMRPNGXPGP-UHFFFAOYSA-N 0.000 description 1
- 238000007046 ethoxylation reaction Methods 0.000 description 1
- 230000004438 eyesight Effects 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- LQJBNNIYVWPHFW-VAWYXSNFSA-N gadelaidic acid Chemical compound CCCCCCCCCC\C=C\CCCCCCCC(O)=O LQJBNNIYVWPHFW-VAWYXSNFSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 229930182478 glucoside Natural products 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 229920001477 hydrophilic polymer Polymers 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- MOYKHGMNXAOIAT-JGWLITMVSA-N isosorbide dinitrate Chemical compound [O-][N+](=O)O[C@H]1CO[C@@H]2[C@H](O[N+](=O)[O-])CO[C@@H]21 MOYKHGMNXAOIAT-JGWLITMVSA-N 0.000 description 1
- 229960000201 isosorbide dinitrate Drugs 0.000 description 1
- 150000002584 ketoses Chemical class 0.000 description 1
- 238000004900 laundering Methods 0.000 description 1
- 229960004232 linoleic acid Drugs 0.000 description 1
- 229960004488 linolenic acid Drugs 0.000 description 1
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- BXWNKGSJHAJOGX-UHFFFAOYSA-N n-hexadecyl alcohol Natural products CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000005677 organic carbonates Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- SECPZKHBENQXJG-FPLPWBNLSA-N palmitoleic acid Chemical compound CCCCCC\C=C/CCCCCCCC(O)=O SECPZKHBENQXJG-FPLPWBNLSA-N 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 239000001259 polydextrose Substances 0.000 description 1
- 229940035035 polydextrose Drugs 0.000 description 1
- 235000013856 polydextrose Nutrition 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229950008882 polysorbate Drugs 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000012797 qualification Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000005201 scrubbing Methods 0.000 description 1
- 230000011218 segmentation Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000000967 suction filtration Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- 229960001124 trientine Drugs 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/34—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups
- C07C233/35—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
- C07C233/36—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/835—Mixtures of non-ionic with cationic compounds
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/165—Ethers
- D06M13/17—Polyoxyalkyleneglycol ethers
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/402—Amides imides, sulfamic acids
- D06M13/405—Acylated polyalkylene polyamines
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/402—Amides imides, sulfamic acids
- D06M13/419—Amides having nitrogen atoms of amide groups substituted by hydroxyalkyl or by etherified or esterified hydroxyalkyl groups
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/42—Ethers, e.g. polyglycol ethers of alcohols or phenols
-
- 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
- C11D1/52—Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
- C11D1/528—Carboxylic amides (R1-CO-NR2R3), where at least one of the chains R1, R2 or R3 is interrupted by a functional group, e.g. a -NH-, -NR-, -CO-, or -CON- group
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/722—Ethers of polyoxyalkylene glycols having mixed oxyalkylene groups; Polyalkoxylated fatty alcohols or polyalkoxylated alkylaryl alcohols with mixed oxyalkylele groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Materials Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Detergent Compositions (AREA)
Abstract
本发明涉及脂肪酸酰胺,它通过脂肪酸或其脂与多价胺缩合而获得,用酸部分中和未反应的氨基基团并加入式(III)的分散促进剂,
其中R4为含12至22个碳原子的烷基和/或链烯基基团,p为零或1至5的数值,q为1至5的数值。脂肪酰胺易于分散在冷水中并宜用于制备纺织品处理剂。
Description
发明范围
本发明是关于具有改进的冷水可分散性的脂肪酸酰胺。它可由脂肪酸或其酯类与多价的胺类缩聚,部分中和并加入选定的分散促进剂而制得。还涉及其制备方法、纺织物处理剂、所制得的所述脂肪酸酰胺及其在制备纺织物处理剂中的应用。
技术背景
目前有很多化合物或混合物被建议用于纺织纤维,纱线或织物的处理,从而使所处理的纺织物具有所希望的性能或作为纺织物保护剂的组成部分。按所用有效物的技术可改善纺织物的加工性能,穿着合适性以及改善其维护性。
例如美国专利文献US2340881中叙述了由羟烷基聚胺和脂肪酸甘油酯所生产的缩合产物的水性分散体,可改善由它处理过的纺织物的光滑性以及柔软性。
US3454494是关于添加一种有分散效用的聚乙二醇醚的脂肪酸缩合产物。
德国专利文献DE-PS1922046叙述了含脂肪酸缩合产物的洗涤剂,从生产过程开始起即含有分散性的脂肪酸甘油酯;德国文献DE-PS1922047中叙述了这种物质也特别可用作液体洗涤处理剂的纺织物软化剂。这些物质以及类似物可通过将其置于热水中,使用高剪切力而分散于水中,或从生产起将尚处于熔融状缩合产物分散于水中。由于必要的费用,多数生产者先将其制成分散体并将分散体供应使用者,它在贮存和运输中都含有大量水份,因此从经济观点看是不经济的。
按德国专利申请DE-Al 3530302,DE-Al 3730792,DE-Al 3901820和DE-Al 4111648(Henkel)在加入适宜的分散加速剂后可改善此类物质的分散性,例如加入葡萄糖,山梨糖醇,甘露糖醇,季戊四醇,烷基聚葡萄糖,山梨糖醇酯,凝胶体以及不饱和脂肪醇和脂肪酸。市场上还有另外产品,将高度乙氧基化的牛脂醇和1,2-丙二醇混合物作为分散促进剂。
虽然如此,但在实际中经常见到脂肪酸和多价胺的缩合产物出现沉淀物,它在水中不分散或分散得不充分。这种产品质量的不稳定性造成经济上明显缺陷,限制了它们作为所要求的纺织物处理剂的可使用性。另一个问题是现有技术的产品本身具有满意的分散性,但当它在空气中贮存后,一般会出现不可逆的损失。
本发明的任务是提供没有上述缺点的新的脂肪酸酰胺。
本发明的说明
本发明的目的是通过下述方法制备具有改进的冷水可分散性的脂肪酸酰胺;将
a)式(I)脂肪酸
R1CO-OH (I)
其中R2为氢,甲基,乙基,羟乙基或-(CH2)n-NHR3基团,R3为氢,甲基,乙基,或羟乙基基团,n为2至4的数值和m为1至4的数值。
b)用酸部分中和未反应的氨基基团
其中R4为含12至22个碳原子的烷基和/或链烯基基团,p为零或1至5的数值,q为1至5的数值。
意外的发现,在缩合产物中加入选定的非离子型表面活性剂,不仅使产物与目前现有技术相比,其分散性具有明显的改进;同时缩合物在空气中贮存较长时间后,依然可保留其优越的性能。
本发明的另一目的是关于制备具有改进的冷水可分散性的脂肪酸酰胺的方法,它通过将
a)式(I)脂肪酸
R1CO-OH (I)
(其中R1CO为一个含8-22个碳原子及O和/或1至3个双键的脂族酰基)或其酯类与式(II)的多价胺类进行缩合
其中R2为氢,甲基,乙基,羟乙基或-(CH2)n-NHR3基团,R3为氢,甲基,乙基或羟乙基基团,n为2至4的数值和m为1至4的数值。
b)用酸部分中和未反应的氨基基团和
其中R4为含12至22个碳原子的烷基和/或链烯基基团,p为零或1至5的数值,q为1至5的数值。
原料
按本发明制备脂肪酸酰胺,将式(I)的脂肪酸作为组份I。典型实例是己酸,癸酸,辛酸,月桂酸,肉豆蔻酸,棕榈酸,棕榈油酸,硬脂酸,异硬酯酸,油酸,反油酸,石芹酸,亚油酸,亚麻酸,桐酸,花生酸,顺(式)9-二十碳烯酸,山萮酸和芥酸以及其工业混合物,例如脂和油类在加压裂化时的产物。加入的脂肪酸也可以呈其C1-4烷基酯的形式,特别是它的甲基酯及其甘油脂,尤其是三酸甘油脂。
优选的是加入式(I)的工业棕榈酸或牛脂酸,其中R1CO为含16至18个碳原子及O和/或1个双键的酰基。
作为式(II)组份的多价胺,优先的同样是羟基取代的乙烯基二胺或二乙烯三胺。典型实例为二羟基乙烯二胺,羟乙基二乙烯二胺,羟丙基二乙烯三胺以及特别是氨基乙基乙醇胺。此外N,N-二甲基-1,3-二氨基丙烷,三乙烯四胺或四乙烯五胺也很适宜。
由所得缩合产物的工业使用性考虑,证明加入式(II)的多价胺是最佳的,其中R2为羟乙基或(CH2)2NH2-基团,R3为氢,n为2和m为1或2的数值。
缩合反应
在制备缩合产物时,例如加入的脂肪酸或其脂类和多价胺的摩尔比为1∶1至2.5∶1,优先的为1.3∶1至1.7∶1。将组份在170℃至210℃,优先的在180℃至200℃加热0.5至5小时,优先的1至2小时直至脂肪酸或脂肪酸酯实际全部反应后,再将混合物在该反应温度下继续反应5至60分钟,优先的为15至30分钟。特别是如果要求制备淡色产物,则建议在排除空气-氧气并在还原剂如次磷酸存在下进行缩合反应。
缩合反应结束时可用低分子有机碳酸,羟基碳酸或无机酸例如醋酸,乳酸或磷酸中和未反应的氨基基团,其中如用计算量酸与脂肪酸缩合产物的融体进行混合而形成盐或者通过在有机酸或一种有机酸的水溶液中溶解或分散反应产物使其形成胺盐。按本发明成盐所需酸的加入量应为中和所需量的20至80摩尔%,优先的为30至60摩尔%。
分散促进剂
作为分散促进剂通常是疏水性的,非离子型的表面活性剂,如按照式(III)化合物。典型实例为平均1摩尔环氧乙烷和2摩尔环氧丙烷;2摩尔环氧乙烷和4摩尔环氧丙烷;5摩尔环氧乙烷和1摩尔环氧丙烷以及2至3摩尔环氧丙烷在C12/18椰子脂肪醇,C16/18-牛脂醇或C16/18棕榈脂肪酸上的加成物。
从所得产品的分散性质考虑,已证明分散促进剂,式(III)中,R4为含12至18个碳原子的烷基基团,其n与m比例处于n∶m=1∶2至5∶1范围内。
分散促进剂加到缩合产物的时间无严格限定,优先的在分散促进剂存在下进行缩合或者当反应结束时将它混入部分中和物中。加入量可为0.5至15,优先为1至10%重量。如有要求时,也可与其它已知的分散促进剂共同使用,例如醛糖和酮糖类型的单糖、经氢化产生的聚羟基化合物、季戊四醇、三甲基丙烷、烷基葡糖苷、脱水山梨醇酯、聚山梨醇酯以及碳水化合物为基的亲水性聚合物或不饱和的醇类或碳酸。
工业上的可应用性
按本发明的脂肪酸酰胺可以成形为粉状,片状或丸状,并易于在水中,特别是在冷水中加工成稳定的分散体。这里只需与水混合,接着轻微搅拌。所制得的分散体特别稳定并不会离析。在纺织领域的很多情况下它可用于在拉伸加工,浸液离心加工,印花薄软绸加工,喷雾加工中的纺织纤维,纱线或织物的处理上。
本发明的另一目的是关于纺织物的处理剂,它含有10至100%(重量),优选为50至95%(重量)的本发明脂肪酸酰胺。
将本发明的纺织处理剂应用于洗涤剂中时它具有改善清洗效果的作用和/或使已洗涤织物有光泽的作用。本发明的纺织处理剂也可用作已洗涤纺织品的后处理剂的组成部分,使纺织品柔软和抗静电。通常可在最后的漂洗槽中对已洗涤的纺织品进行后处理,但也可在自动洗涤干燥器中在干燥时进行,既可在干燥时喷洒该制剂的分散体或者利用柔韧的纺织品所形成的表面,作为载体作用到基质上。
本发明的另一目的是应用本发明的脂肪酸酰胺生产纺织品处理剂,以在纺织物洗涤时以及洗涤物的后处理时提高纤维,纱线或者织物的质量,它的含量可为所得制剂的固体物含量的10至100%(重量),特别是50%至95%(重量)。
下面的实施例进一步说明本发明的目的,但不局限于此。
实施例I、制备实例
实施例1:
在一个带有搅拌器,温度计,气体导管和蒸馏顶管的4升—四颈圆底烧瓶中将2410克(8.9mol)的工业硬脂酸在通氮气下融熔。在80℃下加入由200.5克(1.95mol)的二乙烯三胺和284.5克(1.95mol)三乙烯四胺组成的混合物。在2小时内将温度升至200℃,并将混合物在搅拌下继续保持1.5小时。最后冷却至120℃。反应过程中馏出物为177克。产品的酸值为4.8,可滴定的氮含量为2.25%(重量)。当达到120℃后加入212.3克醋酸以部分中和产物,得到2908克脆性固体物。
实施例2:
按实例1所获得的560克产物在120℃下加入由2mol环氧乙烷和4mol环氧丙烷与一种C12/18椰子脂肪醇形成的加成物60克(Dehypon(R)LT 24,Henkel K Ga A,Düsseldorf/FRG)。最后产物在冷却辊上形成鳞片状。按DIN 53 989的Dehypon(R)LT24浊度滴定值(TTV)为17.8。
实施例3:
以60克由2mol环氧乙烷与工业十六烷基/油醇(Dehypon(R)OCP502 Henkel K Ga A,杜塞坦夫/联邦德国)组成的加成物重复实例2的试验。其Dehypon(R)OCP 502的浊度滴定值(TTV)为11.5。
参比例VI:
用60克由40mol环氧乙烷与C16/18牛脂脂肪醇所组成的加成物以及33.4克1,2-丙二醇重复实例2试验。
实施例4:
类似于实施例1,将378克(1.4mol)的工业用硬脂酸融熔,在80℃下与97.5克(0.94mol)氨基乙基乙醇胺反应。在1.5小时内将混合物加热到180℃,在该温度下一直搅拌,直至酸值降到5.5。反应过程中得到26.4克馏出物。冷却至110℃的融熔体用20.5克乳酸部分中和(中和度:约80%)并用30克由2mol环氧乙烷在工业用十六烷/油醇(Dehypon(R)OCP 502 Henkel K Ga A,杜塞坦夫/联邦德国)上的加成物混合。最后将产物置于冷却辊上制成片。II、分散性的检测
a)细度的评测
7.5克片状产品置于125毫升长颈有螺旋盖的瓶中,加入92.5克水(30℃,14°d),将瓶子盖紧,短时旋转,存放16个小时。再次旋转晃动后用黑色聚酰胺织物的细滤网布的吸滤器在150毫巴下抽滤,在织物上干燥后用视力评测滤渣的细度从刻度1(最细分散)至6(粗分散,很大的团块)之间。其结果列于表1。
b)空气下存放后评定
10克鳞片状产物在10厘米直径的瓷盘里在空气下存放5天(相对湿度为30-40%)而进行评断。结果列于表1。
表1:细度评定
实例 细度
16小时后 5天后
2 2 3
3 2 2
4 2 2
VI 4.5 6
Claims (12)
1、具有改进的冷水可分散性的脂肪酰胺,它由下述方法得到:
a)式(I)的脂肪酸
R1CO-OH (I)
(其中R1CO为一个含8至22个碳原子,并有O和/或1至3个双键的一种脂族酰基基团)或其酯类与式(II)的多价胺进行缩合:
其中R2为氢,甲基,乙基,羟乙基或-(CH2)n-NHR3的基团,R3为氢,甲基,乙基,或羟乙基基团,n为2至4的数值和m为1至4的数值。
b)用酸部分中和未反应的氨基基团
c)加入式(III)的分散促进剂,
其中R4为含12至22碳原子的烷基和/或链烯基基团,P为零或1至5的数值,q为1至5的数值。
3、按权利要求2的方法,其特征在于,加入式(I)的脂肪酸,其中R1CO为含16至18个碳原子以及O和/或1个双键的酰基基团。
4、按权利要求2和3的方法,其特征在于,加入式(II)的多价胺,其中R2为羟乙基或(CH2)NH2基团,R3为氢,n为2和m为1或2的数值。
5、按权利要求2至4的方法,其特征在于,按1∶1至2.5∶1的摩尔比例加入脂肪酸或其酯类和多价胺。
6、按权利要求2至5的方法,其特征在于,在温度为170℃至210℃之间,进行0.5至5小时的缩聚反应。
7、按权利要求2至6的方法,其特征在于,将未反应的氨基基团中和20摩尔%到80摩尔%。
8、按权利要求2至7的方法,其特征在于,用醋酸,乳酸和/或磷酸中和未反应的氨基基团。
9、按权利要求2至8的方法,其特征在于,加入式(III)的分散促进剂,其中R4为含12至18个碳原子的烷基基团,n∶m之比为1∶2至5∶1的范围内。
10、按权利要求2至9的方法,其特征在于,分散促进剂的加入量为0.5至15%(重量)。
11、纺织纤维处理剂,它含有10至100%(重量)的权利要求1的脂肪酸酰胺。
12、按权利要求1的脂肪酸酰胺在制备纺织纤维处理剂中的应用。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4312008A DE4312008A1 (de) | 1993-04-13 | 1993-04-13 | Fettsäureamide |
DEP4312008.3 | 1993-04-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
CN1120836A true CN1120836A (zh) | 1996-04-17 |
Family
ID=6485351
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN94191762A Pending CN1120836A (zh) | 1993-04-13 | 1994-04-05 | 具有改进的冷水可分散性的脂肪酸酰胺 |
Country Status (7)
Country | Link |
---|---|
EP (1) | EP0694031B1 (zh) |
JP (1) | JPH08508740A (zh) |
CN (1) | CN1120836A (zh) |
AT (1) | ATE184590T1 (zh) |
DE (2) | DE4312008A1 (zh) |
ES (1) | ES2138078T3 (zh) |
WO (1) | WO1994024092A1 (zh) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103352367A (zh) * | 2013-05-31 | 2013-10-16 | 浙江安诺其助剂有限公司 | 一种冷水速溶弱阳离子柔软片及其制备方法 |
CN106634934A (zh) * | 2016-11-24 | 2017-05-10 | 贵州黔晟新能源实业有限公司 | 一种环保型醇基压裂液及其制备方法 |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19756680A1 (de) * | 1997-12-19 | 1999-06-24 | Henkel Kgaa | Fettsäureamidoamide |
CN103321042B (zh) * | 2013-05-31 | 2016-05-18 | 浙江安诺其助剂有限公司 | 一种低温速溶咪唑啉季铵盐阳离子柔软片及其制备方法 |
JP6446744B2 (ja) * | 2017-01-26 | 2019-01-09 | 株式会社先進工学研究所 | 脂肪酸アミドの製造方法 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3454494A (en) * | 1965-08-03 | 1969-07-08 | Standard Chem Products Inc | Textile softener compositions |
DE2911198C2 (de) * | 1979-03-22 | 1982-10-07 | Dalli-Werke Mäurer & Wirtz, 5190 Stolberg | Konzentrierte Wäscheweichspülmittel und Verfahren zu deren Herstellung |
DE3411328A1 (de) * | 1984-03-28 | 1985-10-10 | Hoechst Ag | Nichtionische, fliessfaehige perlglanzdispersionen |
US4668423A (en) * | 1985-04-19 | 1987-05-26 | Sherex Chemical Company | Liquid biodegradable surfactant and use thereof |
DE3901820A1 (de) * | 1989-01-23 | 1990-08-09 | Henkel Kgaa | Textilbehandlungsmittel |
DE4111648A1 (de) * | 1991-04-10 | 1992-10-15 | Henkel Kgaa | Textilbehandlungsmittel mit verbesserter wasserdispergierbarkeit |
DE4125025A1 (de) * | 1991-07-29 | 1993-02-04 | Henkel Kgaa | Fluessiges waschmittel |
-
1993
- 1993-04-13 DE DE4312008A patent/DE4312008A1/de not_active Withdrawn
-
1994
- 1994-04-05 DE DE59408751T patent/DE59408751D1/de not_active Expired - Fee Related
- 1994-04-05 CN CN94191762A patent/CN1120836A/zh active Pending
- 1994-04-05 AT AT94913528T patent/ATE184590T1/de not_active IP Right Cessation
- 1994-04-05 WO PCT/EP1994/001051 patent/WO1994024092A1/de active IP Right Grant
- 1994-04-05 ES ES94913528T patent/ES2138078T3/es not_active Expired - Lifetime
- 1994-04-05 JP JP6522694A patent/JPH08508740A/ja active Pending
- 1994-04-05 EP EP94913528A patent/EP0694031B1/de not_active Expired - Lifetime
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103352367A (zh) * | 2013-05-31 | 2013-10-16 | 浙江安诺其助剂有限公司 | 一种冷水速溶弱阳离子柔软片及其制备方法 |
CN103352367B (zh) * | 2013-05-31 | 2015-05-27 | 浙江安诺其助剂有限公司 | 一种冷水速溶弱阳离子柔软片及其制备方法 |
CN106634934A (zh) * | 2016-11-24 | 2017-05-10 | 贵州黔晟新能源实业有限公司 | 一种环保型醇基压裂液及其制备方法 |
Also Published As
Publication number | Publication date |
---|---|
EP0694031B1 (de) | 1999-09-15 |
EP0694031A1 (de) | 1996-01-31 |
DE59408751D1 (de) | 1999-10-21 |
ATE184590T1 (de) | 1999-10-15 |
DE4312008A1 (de) | 1994-10-20 |
JPH08508740A (ja) | 1996-09-17 |
ES2138078T3 (es) | 2000-01-01 |
WO1994024092A1 (de) | 1994-10-27 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
FI79137B (fi) | Tvaettmedelkompositioner, som innehaoller ytaktivt medel och aminoxidpolymer. | |
JPH06503841A (ja) | 組成物およびそれで処理された重合体織物 | |
JPH073645A (ja) | 液体柔軟仕上剤組成物 | |
JPH0765267B2 (ja) | 柔軟仕上剤 | |
US4786439A (en) | Textile treatment composition | |
CN1120836A (zh) | 具有改进的冷水可分散性的脂肪酸酰胺 | |
JP5577090B2 (ja) | 液体洗浄剤組成物 | |
JP5073201B2 (ja) | 衣料用液体洗浄剤組成物 | |
JP2001247528A (ja) | 脂肪酸n−アルキルポリヒドロキシアミドの製造方法 | |
US20020002297A1 (en) | Polyquaternaries from mdea using dibasic acids and fatty acids | |
KR970011243B1 (ko) | 텍스타일 처리 제제 | |
EP0707059B1 (en) | Liquid softener composition | |
US9593208B2 (en) | Polysiloxanes with quaternized heterocyclic groups | |
US4865768A (en) | Phosphoric acid salt of the reaction product of a mono-carboxylic acid with a polyamine | |
GB2203177A (en) | Softener compositions containing acylated polyamines | |
JP2008007707A (ja) | 液体洗浄剤組成物 | |
JP3755443B2 (ja) | 古紙再生用添加剤及び再生紙の製造方法 | |
JPH06506730A (ja) | 繊維製品用柔軟剤としてのエステルの使用 | |
JP4342650B2 (ja) | 合成繊維用処理剤及び合成繊維の処理方法 | |
DE19902506A1 (de) | Hydrophobierungsmittel für harte Oberflächen | |
US5888949A (en) | Composition for cleaning textile dyeing machines | |
US20060047141A1 (en) | Method for producing light coloured polyalkylene glycol diethyl ether of fatty acid alcanolamine | |
JP2951776B2 (ja) | 液体柔軟仕上剤 | |
DE19756680A1 (de) | Fettsäureamidoamide | |
JPH0657632A (ja) | 柔軟仕上剤 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C01 | Deemed withdrawal of patent application (patent law 1993) | ||
WD01 | Invention patent application deemed withdrawn after publication |