EP0307748A2 - Agent pour traiter des tissus - Google Patents

Agent pour traiter des tissus Download PDF

Info

Publication number: EP0307748A2
Authority: EP; European Patent Office
Prior art keywords: textile treatment; treatment agent; dispersion; agent according; accelerator
Prior art date: 1987-09-14
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 Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Withdrawn

Application number

EP88114457A

Other languages

German (de)

English (en)

Other versions

EP0307748A3 (fr

Inventor

Uwe Dr. Ploog

Günter Uphues

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Henkel AG and Co KGaA

Original Assignee

Henkel AG and Co KGaA

Priority date (The priority date 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 date listed.)

1987-09-14

Filing date

1988-09-05

Publication date

1989-03-22

1988-09-05 Application filed by Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA

1989-03-22 Publication of EP0307748A2 publication Critical patent/EP0307748A2/fr

1990-03-21 Publication of EP0307748A3 publication Critical patent/EP0307748A3/fr

Status Withdrawn legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims description 15
239000004744 fabric Substances 0.000 title claims description 8
239000004753 textile Substances 0.000 claims abstract description 58
239000003795 chemical substances by application Substances 0.000 claims abstract description 53
239000006185 dispersion Substances 0.000 claims abstract description 38
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 23
-1 aliphatic monocarboxylic acids Chemical class 0.000 claims abstract description 11
150000002772 monosaccharides Chemical class 0.000 claims abstract description 10
238000005984 hydrogenation reaction Methods 0.000 claims abstract description 9
229920000768 polyamine Polymers 0.000 claims abstract description 9
125000003277 amino group Chemical group 0.000 claims abstract description 8
125000002768 hydroxyalkyl group Chemical group 0.000 claims abstract description 8
238000006243 chemical reaction Methods 0.000 claims abstract description 7
239000011541 reaction mixture Substances 0.000 claims abstract description 7
150000001875 compounds Chemical class 0.000 claims abstract description 5
238000006386 neutralization reaction Methods 0.000 claims abstract description 5
235000014113 dietary fatty acids Nutrition 0.000 claims description 29
239000000194 fatty acid Substances 0.000 claims description 29
229930195729 fatty acid Natural products 0.000 claims description 29
150000004665 fatty acids Chemical class 0.000 claims description 29
239000000047 product Substances 0.000 claims description 21
239000007859 condensation product Substances 0.000 claims description 20
238000000034 method Methods 0.000 claims description 14
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 claims description 13
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 claims description 13
239000000600 sorbitol Substances 0.000 claims description 13
125000004432 carbon atom Chemical group C* 0.000 claims description 8
108010010803 Gelatin Proteins 0.000 claims description 7
239000008273 gelatin Substances 0.000 claims description 7
229920000159 gelatin Polymers 0.000 claims description 7
235000019322 gelatine Nutrition 0.000 claims description 7
235000011852 gelatine desserts Nutrition 0.000 claims description 7
239000000835 fiber Substances 0.000 claims description 6
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 6
JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 claims description 5
238000006482 condensation reaction Methods 0.000 claims description 5
229920001477 hydrophilic polymer Polymers 0.000 claims description 5
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 claims description 4
229930195725 Mannitol Natural products 0.000 claims description 4
239000000594 mannitol Substances 0.000 claims description 4
235000010355 mannitol Nutrition 0.000 claims description 4
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 claims description 3
208000007976 Ketosis Diseases 0.000 claims description 3
150000001323 aldoses Chemical class 0.000 claims description 3
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 claims description 3
239000008103 glucose Substances 0.000 claims description 3
229930182470 glycoside Natural products 0.000 claims description 3
150000002584 ketoses Chemical class 0.000 claims description 3
229920005862 polyol Polymers 0.000 claims description 3
150000003077 polyols Chemical class 0.000 claims description 3
150000001408 amides Chemical class 0.000 claims description 2
229930182478 glucoside Natural products 0.000 claims description 2
238000000465 moulding Methods 0.000 claims description 2
239000000843 powder Substances 0.000 claims description 2
238000005406 washing Methods 0.000 claims description 2
239000000654 additive Substances 0.000 claims 1
239000011872 intimate mixture Substances 0.000 claims 1
238000002360 preparation method Methods 0.000 claims 1
229920005615 natural polymer Polymers 0.000 abstract description 2
229920001059 synthetic polymer Polymers 0.000 abstract 1
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 21
AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 18
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 16
239000003599 detergent Substances 0.000 description 10
238000007792 addition Methods 0.000 description 9
229910052757 nitrogen Inorganic materials 0.000 description 8
239000002253 acid Substances 0.000 description 7
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 6
238000012360 testing method Methods 0.000 description 6
150000001412 amines Chemical class 0.000 description 5
239000003760 tallow Substances 0.000 description 5
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
239000004480 active ingredient Substances 0.000 description 4
LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 description 4
150000001735 carboxylic acids Chemical class 0.000 description 4
239000007795 chemical reaction product Substances 0.000 description 4
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
238000004519 manufacturing process Methods 0.000 description 4
238000003756 stirring Methods 0.000 description 4
229920000742 Cotton Polymers 0.000 description 3
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
235000021355 Stearic acid Nutrition 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
238000001035 drying Methods 0.000 description 3
239000003205 fragrance Substances 0.000 description 3
239000000155 melt 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
ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 3
239000008117 stearic acid Substances 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
229910000147 aluminium phosphate Inorganic materials 0.000 description 2
235000015278 beef Nutrition 0.000 description 2
239000003638 chemical reducing agent Substances 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
150000002191 fatty alcohols Chemical class 0.000 description 2
125000000524 functional group Chemical group 0.000 description 2
IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
239000004310 lactic acid Substances 0.000 description 2
235000014655 lactic acid Nutrition 0.000 description 2
238000002156 mixing Methods 0.000 description 2
230000003472 neutralizing effect Effects 0.000 description 2
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
230000003287 optical effect Effects 0.000 description 2
150000007524 organic acids Chemical class 0.000 description 2
VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
238000009988 textile finishing Methods 0.000 description 2
ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 1
SOIAEOTUSNFHMI-UHFFFAOYSA-N 2-(2-aminoethylamino)ethane-1,1-diol Chemical compound NCCNCC(O)O SOIAEOTUSNFHMI-UHFFFAOYSA-N 0.000 description 1
HVOBSBRYQIYZNY-UHFFFAOYSA-N 2-[2-(2-aminoethylamino)ethylamino]ethanol Chemical compound NCCNCCNCCO HVOBSBRYQIYZNY-UHFFFAOYSA-N 0.000 description 1
TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-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
244000215068 Acacia senegal Species 0.000 description 1
229920001817 Agar Polymers 0.000 description 1
235000021357 Behenic acid Nutrition 0.000 description 1
229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
235000013162 Cocos nucifera Nutrition 0.000 description 1
244000060011 Cocos nucifera Species 0.000 description 1
244000303965 Cyamopsis psoralioides Species 0.000 description 1
239000004375 Dextrin Substances 0.000 description 1
229920001353 Dextrin Polymers 0.000 description 1
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
229930091371 Fructose Natural products 0.000 description 1
RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
239000005715 Fructose Substances 0.000 description 1
241000206672 Gelidium Species 0.000 description 1
229920000084 Gum arabic Polymers 0.000 description 1
LKDRXBCSQODPBY-AMVSKUEXSA-N L-(-)-Sorbose Chemical compound OCC1(O)OC[C@H](O)[C@@H](O)[C@@H]1O LKDRXBCSQODPBY-AMVSKUEXSA-N 0.000 description 1
239000005639 Lauric acid Substances 0.000 description 1
239000004435 Oxo alcohol Substances 0.000 description 1
235000021314 Palmitic acid Nutrition 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
235000019484 Rapeseed oil Nutrition 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
NWGKJDSIEKMTRX-AAZCQSIUSA-N Sorbitan monooleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-AAZCQSIUSA-N 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
239000000205 acacia gum Substances 0.000 description 1
235000010489 acacia gum Nutrition 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
235000010419 agar Nutrition 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
229940116226 behenic acid Drugs 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
239000005018 casein Substances 0.000 description 1
BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
235000021240 caseins Nutrition 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
238000004140 cleaning Methods 0.000 description 1
229940096386 coconut alcohol Drugs 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
239000006071 cream Substances 0.000 description 1
235000019425 dextrin Nutrition 0.000 description 1
238000004821 distillation Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
239000002979 fabric softener Substances 0.000 description 1
238000007667 floating Methods 0.000 description 1
238000009472 formulation Methods 0.000 description 1
125000005456 glyceride group Chemical group 0.000 description 1
235000011187 glycerol Nutrition 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
239000012943 hotmelt Substances 0.000 description 1
238000007654 immersion Methods 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000004584 polyacrylic acid Substances 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
239000001267 polyvinylpyrrolidone Substances 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
230000002335 preservative effect Effects 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
238000010992 reflux Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
235000003441 saturated fatty acids Nutrition 0.000 description 1
150000004671 saturated fatty acids Chemical class 0.000 description 1
239000000344 soap Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000001593 sorbitan monooleate Substances 0.000 description 1
235000011069 sorbitan monooleate Nutrition 0.000 description 1
229940035049 sorbitan monooleate Drugs 0.000 description 1
229950004959 sorbitan oleate Drugs 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000000758 substrate Substances 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
238000004448 titration Methods 0.000 description 1
JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical compound OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1
239000001226 triphosphate Substances 0.000 description 1
235000011178 triphosphate Nutrition 0.000 description 1
UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 1
150000004670 unsaturated fatty acids Chemical class 0.000 description 1
235000021122 unsaturated fatty acids Nutrition 0.000 description 1

Classifications

- 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
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
- D06M15/423—Amino-aldehyde resins
- D06M15/45—Use of special catalysts
- 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
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2003—Alcohols; Phenols
- C11D3/2065—Polyhydric alcohols
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/22—Carbohydrates or derivatives thereof
- C11D3/221—Mono, di- or trisaccharides or derivatives thereof
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/22—Carbohydrates or derivatives thereof
- C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/662—Carbohydrates or derivatives
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/667—Neutral esters, e.g. sorbitan esters

Definitions

a textile treatment agent which can be prepared by reacting a) aliphatic monocarboxylic acids having 8 to 22 carbon atoms or derivatives forming amides with b) hydroxyalkylpolyamines and subsequent neutralization of unreacted amino groups, the textile treatment agent being an addition of dispersion accelerators selected from the group of Monosaccharides of the aldose and ketose type and the polyhydroxy compounds derived therefrom by hydrogenation, the polyols, such as in particular pentaerythritol, the alkylglycosides, the sorbitan esters and the natural and synthetic hydrophilic polymers in such Amounts contain that the textile treatment agents can be dispersed quickly in cold water in a short time, characterized in that the dispersion accelerator is already contained in the reaction mixture during the reaction.
Amide-forming derivatives of aliphatic monocarboxylic acids are understood to mean the esters derived from natural or synthetic fatty acids or fatty acid mixtures with lower alkanols such as, for example, methanol or ethanol, the fatty acid glycerides and the fatty acid halides.
these are the derivatives derived from lauric acid, myristic acid, palmitic acid, stearic acid, coconut fatty acid, tallow fatty acid or rapeseed oil fatty acid.
the reaction products which can be produced from this by reaction with hydroxyalkyl polyamines are referred to below as fatty acid condensation products.
Suitable hydroxyalkyl polyamines are preferably derived from the hydroxyalkyl derivatives of ethylene diamine or diethylene triamine, e.g. from dihydroxyethylethylenediamine, hydroxyethyldiethylenetriamine, hydroxypropyldiethylenetriamine, and especially hydroxyethylethylenediamine.
Lower carboxylic acids in particular low molecular weight organic mono- or polycarboxylic acids which are optionally substituted by hydroxyl groups, such as, for example, glycolic acid, citric acid, lactic acid or acetic acid, are suitable for neutralizing unreacted amino groups.
Suitable alkyl glycosides are obtained by the Fischer process by reacting monosaccharide with fatty alcohol in the presence of an acidic catalyst.
Alkyl glycosides, the alkyl group of which contains up to 16 carbon atoms, have long been known as surfactants.
Suitable sorbitan esters are esters with saturated or unsaturated fatty acids having 10 to 20 carbon atoms, in particular sorbitan oleate.

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Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Engineering & Computer Science (AREA)
Organic Chemistry (AREA)
Wood Science & Technology (AREA)
Oil, Petroleum & Natural Gas (AREA)
Health & Medical Sciences (AREA)
Emergency Medicine (AREA)
Molecular Biology (AREA)
Textile Engineering (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Compositions Of Macromolecular Compounds (AREA)

EP88114457A 1987-09-14 1988-09-05 Agent pour traiter des tissus Withdrawn EP0307748A3 (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE3730792		1987-09-14
DE19873730792 DE3730792A1 (de)	1987-09-14	1987-09-14	Textilbehandlungsmittel

Publications (2)

Publication Number	Publication Date
EP0307748A2 true EP0307748A2 (fr)	1989-03-22
EP0307748A3 EP0307748A3 (fr)	1990-03-21

Family

ID=6335948

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
EP88114457A Withdrawn EP0307748A3 (fr)	1987-09-14	1988-09-05	Agent pour traiter des tissus

Country Status (9)

Country	Link
US (1)	US4877539A (fr)
EP (1)	EP0307748A3 (fr)
JP (1)	JPH01156577A (fr)
KR (1)	KR890005340A (fr)
BR (1)	BR8804733A (fr)
DE (1)	DE3730792A1 (fr)
DK (1)	DK509488A (fr)
TR (1)	TR23666A (fr)
ZA (1)	ZA886826B (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO1992018685A1 (fr) *	1991-04-10	1992-10-29	Henkel Kommanditgesellschaft Auf Aktien	Produit de traitement des textiles a dispersibilite amelioree dans l'eau
EP0618286A1 (fr) *	1993-03-30	1994-10-05	AUSIMONT S.p.A.	Méthode pour réduire la formation de dépôt d'incrustations inorganiques sur les textiles et mélange de détergents utilisés dans ce procédé

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3901820A1 (de) *	1989-01-23	1990-08-09	Henkel Kgaa	Textilbehandlungsmittel
GB8916308D0 (en) *	1989-07-17	1989-08-31	Unilever Plc	Fabric softening
JPH0768669B2 (ja) *	1990-10-05	1995-07-26	花王株式会社	濃縮型柔軟仕上剤
US5296024A (en) *	1991-08-21	1994-03-22	Sequa Chemicals, Inc.	Papermaking compositions, process using same, and paper produced therefrom
US5292363A (en) *	1991-08-21	1994-03-08	Sequa Chemicals, Inc.	Papermarking composition, process using same, and paper produced therefrom
US5478387A (en) *	1994-04-18	1995-12-26	Sequa Chemicals, Inc.	Opacifying composition for paper
DE19626317A1 (de) *	1996-07-01	1998-01-08	Basf Ag	Kondensationsprodukte von Fettsäuren mit Aminoalkoholen und Polyolen und ihre Verwendung als Textilhilfsmittel
US5711958A (en) *	1996-07-11	1998-01-27	Life Medical Sciences, Inc.	Methods for reducing or eliminating post-surgical adhesion formation
US6696499B1 (en) *	1996-07-11	2004-02-24	Life Medical Sciences, Inc.	Methods and compositions for reducing or eliminating post-surgical adhesion formation
US6211249B1 (en)	1997-07-11	2001-04-03	Life Medical Sciences, Inc.	Polyester polyether block copolymers

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2340881A (en) *	1939-08-22	1944-02-08	Nat Oil Prod Co	Composition for lubricating and softening textile fibers
US3454494A (en) *	1965-08-03	1969-07-08	Standard Chem Products Inc	Textile softener compositions
DE3501521A1 (de) *	1985-01-18	1986-07-24	Henkel KGaA, 4000 Düsseldorf	Waessriges konzentriertes textilweichmachungsmittel
DE3530302A1 (de) *	1985-08-24	1987-03-05	Henkel Kgaa	Textilbehandlungsmittel

1987
- 1987-09-14 DE DE19873730792 patent/DE3730792A1/de not_active Withdrawn
1988
- 1988-07-13 TR TR50688A patent/TR23666A/xx unknown
- 1988-09-05 EP EP88114457A patent/EP0307748A3/fr not_active Withdrawn
- 1988-09-13 ZA ZA886826A patent/ZA886826B/xx unknown
- 1988-09-13 US US07/243,956 patent/US4877539A/en not_active Expired - Fee Related
- 1988-09-13 DK DK509488A patent/DK509488A/da not_active Application Discontinuation
- 1988-09-14 JP JP63231397A patent/JPH01156577A/ja active Pending
- 1988-09-14 BR BR8804733A patent/BR8804733A/pt unknown
- 1988-09-14 KR KR1019880011862A patent/KR890005340A/ko not_active Withdrawn

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO1992018685A1 (fr) *	1991-04-10	1992-10-29	Henkel Kommanditgesellschaft Auf Aktien	Produit de traitement des textiles a dispersibilite amelioree dans l'eau
EP0618286A1 (fr) *	1993-03-30	1994-10-05	AUSIMONT S.p.A.	Méthode pour réduire la formation de dépôt d'incrustations inorganiques sur les textiles et mélange de détergents utilisés dans ce procédé
US5496494A (en) *	1993-03-30	1996-03-05	Ausimont S.P.A.	Process for decreasing the build up of inorganic incrustations on textiles and detergent composition used in such process

Also Published As

Publication number	Publication date
DK509488A (da)	1989-03-15
DK509488D0 (da)	1988-09-13
JPH01156577A (ja)	1989-06-20
EP0307748A3 (fr)	1990-03-21
DE3730792A1 (de)	1989-03-23
KR890005340A (ko)	1989-05-13
BR8804733A (pt)	1989-04-18
US4877539A (en)	1989-10-31
TR23666A (tr)	1990-06-04
ZA886826B (en)	1989-05-30

Publication	Publication Date	Title
EP0213519B1 (fr)	1992-12-02	Produit de traitement de textile
EP0413249B1 (fr)	1997-12-10	Adoucissant pour textile
EP0569869B1 (fr)	1999-01-13	Composés d'amides de l'acide lactobionique et leur utilisation
DE2631114A1 (de)	1977-02-10	Gewebeweichmacher
DE2622014A1 (de)	1976-12-02	Textilbehandlungsmittel
EP0307748A2 (fr)	1989-03-22	Agent pour traiter des tissus
DE69109579T2 (de)	1995-12-21	Textilweichmacherzusammensetzung.
EP0507003A2 (fr)	1992-10-07	Nouveaux composés d'ammonium, procédé pour leur préparation et leur utilisation comme agents de nettoyage, matériaux bruts pour cosmétiques et agents d'adoucissement, sûrtout comme agents de tissage pour textiles
DE2615704C2 (fr)	1988-10-27
DE2543636C3 (de)	1981-05-07	Flüssiges wäßriges Weichmachungsmittel
DE69101456T2 (de)	1994-07-14	Flüssige Textilweichmacherzusammensetzung.
EP0454741B1 (fr)	1993-06-02	Agents de traitement de textiles
DE3730444C2 (fr)	1992-08-20
EP0230910B2 (fr)	1997-01-15	Moyen pour le traitement de matières textiles
EP2465917A1 (fr)	2012-06-20	Plastifiant pour textiles
DE1619182C3 (de)	1978-03-02	Verfahren zum Weichmachen von Textilien
EP0694031B1 (fr)	1999-09-15	Procédé pour la préparation d'amides d'acides gras et leur utilisation
DE1959651B2 (de)	1973-04-26	Verfahren zur herstellung langkettiger alkylol- und acylgruppen enthaltender oligopeptidderivate
DE3539570A1 (de)	1987-05-14	Quartaere ammoniumverbindungen, deren herstellung und verwendung als textilweichmacher
DE2539310A1 (de)	1977-03-17	Textilweichmacher
WO1992003526A1 (fr)	1992-03-05	Utilisation de produits de reaction de graisses naturelles comme agents adoucissants de textiles
EP0316701A2 (fr)	1989-05-24	Sels quaternaires d'amidoammonium, procédé de préparation et utilisation
WO1999032432A1 (fr)	1999-07-01	Aminoamides d'acide gras a dispersibilite amelioree
DE2333564A1 (de)	1975-01-30	Textilbehandlungsmittel zur verbesserung der auswaschbarkeit von verschutzungen
DE2126397B2 (de)	1973-08-16	Verfahren zur herstellung neuer oligopeptidderivate

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1993-05-19	17Q	First examination report despatched	Effective date: 19930405
1993-05-19	18W	Application withdrawn	Withdrawal date: 19930329