JPH01272888A - Soaping agent and treatment using the same - Google Patents
Soaping agent and treatment using the sameInfo
- Publication number
- JPH01272888A JPH01272888A JP63101597A JP10159788A JPH01272888A JP H01272888 A JPH01272888 A JP H01272888A JP 63101597 A JP63101597 A JP 63101597A JP 10159788 A JP10159788 A JP 10159788A JP H01272888 A JPH01272888 A JP H01272888A
- Authority
- JP
- Japan
- Prior art keywords
- soaping
- acid
- dyed
- fatty acids
- fatty acid
- 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
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 38
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 28
- 239000000194 fatty acid Substances 0.000 claims abstract description 28
- 229930195729 fatty acid Natural products 0.000 claims abstract description 28
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 28
- 150000003839 salts Chemical class 0.000 claims abstract description 19
- 229920003043 Cellulose fiber Polymers 0.000 claims abstract description 14
- 239000000985 reactive dye Substances 0.000 claims abstract description 6
- 238000004043 dyeing Methods 0.000 claims description 27
- 239000000835 fiber Substances 0.000 claims description 21
- 238000000034 method Methods 0.000 claims description 19
- 239000004744 fabric Substances 0.000 abstract description 21
- 239000000975 dye Substances 0.000 abstract description 18
- 235000021122 unsaturated fatty acids Nutrition 0.000 abstract description 14
- 150000004670 unsaturated fatty acids Chemical class 0.000 abstract description 14
- -1 alkali metal salt Chemical class 0.000 abstract description 10
- 229920000742 Cotton Polymers 0.000 abstract description 6
- 229910052783 alkali metal Inorganic materials 0.000 abstract description 5
- 230000000694 effects Effects 0.000 abstract description 5
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 abstract description 4
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 abstract description 4
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 abstract description 3
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 abstract description 3
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 abstract description 3
- 239000005642 Oleic acid Substances 0.000 abstract description 3
- 238000010186 staining Methods 0.000 abstract description 3
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 abstract description 2
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 abstract description 2
- 235000020778 linoleic acid Nutrition 0.000 abstract description 2
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 abstract description 2
- 239000002994 raw material Substances 0.000 abstract description 2
- 241001248531 Euchloe <genus> Species 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- 230000001609 comparable effect Effects 0.000 abstract 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 abstract 1
- 239000004627 regenerated cellulose Substances 0.000 abstract 1
- 239000002253 acid Substances 0.000 description 24
- 238000012360 testing method Methods 0.000 description 24
- 238000005406 washing Methods 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 9
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 8
- CFQZKFWQLAHGSL-FNTYJUCDSA-N (3e,5e,7e,9e,11e,13e,15e,17e)-18-[(3e,5e,7e,9e,11e,13e,15e,17e)-18-[(3e,5e,7e,9e,11e,13e,15e)-octadeca-3,5,7,9,11,13,15,17-octaenoyl]oxyoctadeca-3,5,7,9,11,13,15,17-octaenoyl]oxyoctadeca-3,5,7,9,11,13,15,17-octaenoic acid Chemical compound OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C CFQZKFWQLAHGSL-FNTYJUCDSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 238000011109 contamination Methods 0.000 description 6
- 239000000539 dimer Substances 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 5
- 238000005187 foaming Methods 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 4
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 4
- 150000007514 bases Chemical class 0.000 description 4
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 4
- 235000003441 saturated fatty acids Nutrition 0.000 description 4
- 150000004671 saturated fatty acids Chemical class 0.000 description 4
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- ZQPPMHVWECSIRJ-MDZDMXLPSA-N elaidic acid Chemical compound CCCCCCCC\C=C\CCCCCCCC(O)=O ZQPPMHVWECSIRJ-MDZDMXLPSA-N 0.000 description 3
- 238000009981 jet dyeing Methods 0.000 description 3
- 239000004753 textile Substances 0.000 description 3
- YWWVWXASSLXJHU-AATRIKPKSA-N (9E)-tetradecenoic acid Chemical compound CCCC\C=C\CCCCCCCC(O)=O YWWVWXASSLXJHU-AATRIKPKSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 235000013351 cheese Nutrition 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 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
- 229960005135 eicosapentaenoic acid Drugs 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- RGTIBVZDHOMOKC-UHFFFAOYSA-N stearolic acid Chemical compound CCCCCCCCC#CCCCCCCCC(O)=O RGTIBVZDHOMOKC-UHFFFAOYSA-N 0.000 description 2
- 210000004243 sweat Anatomy 0.000 description 2
- GWHCXVQVJPWHRF-KTKRTIGZSA-N (15Z)-tetracosenoic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCCCC(O)=O GWHCXVQVJPWHRF-KTKRTIGZSA-N 0.000 description 1
- 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
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
- ZONJATNKKGGVSU-UHFFFAOYSA-N 14-methylpentadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCC(O)=O ZONJATNKKGGVSU-UHFFFAOYSA-N 0.000 description 1
- AZXGXVQWEUFULR-UHFFFAOYSA-N 2',4',5',7'-tetrabromofluorescein Chemical compound OC(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C(O)=C(Br)C=C21 AZXGXVQWEUFULR-UHFFFAOYSA-N 0.000 description 1
- NNERWURVSCBMJE-UHFFFAOYSA-N 2-oxospiro[1h-indole-3,2'-1h-quinazoline]-4'-carboxylic acid Chemical group O=C1NC2=CC=CC=C2C11N=C(C(=O)O)C2=CC=CC=C2N1 NNERWURVSCBMJE-UHFFFAOYSA-N 0.000 description 1
- YWWVWXASSLXJHU-UHFFFAOYSA-N 9E-tetradecenoic acid Natural products CCCCC=CCCCCCCCC(O)=O YWWVWXASSLXJHU-UHFFFAOYSA-N 0.000 description 1
- 229910015900 BF3 Inorganic materials 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 101100117236 Drosophila melanogaster speck gene Proteins 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 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 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 description 1
- XJXROGWVRIJYMO-SJDLZYGOSA-N Nervonic acid Natural products O=C(O)[C@@H](/C=C/CCCCCCCC)CCCCCCCCCCCC XJXROGWVRIJYMO-SJDLZYGOSA-N 0.000 description 1
- SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 150000001218 Thorium Chemical class 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 235000021322 Vaccenic acid Nutrition 0.000 description 1
- UWHZIFQPPBDJPM-FPLPWBNLSA-M Vaccenic acid Natural products CCCCCC\C=C/CCCCCCCCCC([O-])=O UWHZIFQPPBDJPM-FPLPWBNLSA-M 0.000 description 1
- 229920006221 acetate fiber Polymers 0.000 description 1
- 239000000980 acid dye Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
- 150000008041 alkali metal carbonates Chemical class 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- JAZBEHYOTPTENJ-JLNKQSITSA-N all-cis-5,8,11,14,17-icosapentaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O JAZBEHYOTPTENJ-JLNKQSITSA-N 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
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- KJDZDTDNIULJBE-QXMHVHEDSA-N cetoleic acid Chemical compound CCCCCCCCCC\C=C/CCCCCCCCCC(O)=O KJDZDTDNIULJBE-QXMHVHEDSA-N 0.000 description 1
- GWHCXVQVJPWHRF-UHFFFAOYSA-N cis-tetracosenoic acid Natural products CCCCCCCCC=CCCCCCCCCCCCCCC(O)=O GWHCXVQVJPWHRF-UHFFFAOYSA-N 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- QKSIFUGZHOUETI-UHFFFAOYSA-N copper;azane Chemical compound N.N.N.N.[Cu+2] QKSIFUGZHOUETI-UHFFFAOYSA-N 0.000 description 1
- 230000007123 defense Effects 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- VUXNZDYAHSFXBM-UHFFFAOYSA-N docos-13-ynoic acid Chemical compound CCCCCCCCC#CCCCCCCCCCCCC(O)=O VUXNZDYAHSFXBM-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- JAZBEHYOTPTENJ-UHFFFAOYSA-N eicosapentaenoic acid Natural products CCC=CCC=CCC=CCC=CCC=CCCCC(O)=O JAZBEHYOTPTENJ-UHFFFAOYSA-N 0.000 description 1
- 235000020673 eicosapentaenoic acid Nutrition 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- 229910001425 magnesium ion Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- CNVZJPUDSLNTQU-SEYXRHQNSA-N petroselinic acid Chemical compound CCCCCCCCCCC\C=C/CCCCC(O)=O CNVZJPUDSLNTQU-SEYXRHQNSA-N 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 150000007519 polyprotic acids Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- HIEHAIZHJZLEPQ-UHFFFAOYSA-M sodium;naphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 HIEHAIZHJZLEPQ-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000000988 sulfur dye Substances 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- SFKTYEXKZXBQRQ-UHFFFAOYSA-J thorium(4+);tetrahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[Th+4] SFKTYEXKZXBQRQ-UHFFFAOYSA-J 0.000 description 1
- UWHZIFQPPBDJPM-BQYQJAHWSA-N trans-vaccenic acid Chemical compound CCCCCC\C=C\CCCCCCCCCC(O)=O UWHZIFQPPBDJPM-BQYQJAHWSA-N 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 229960002703 undecylenic acid Drugs 0.000 description 1
- JXUKQCUPTNLTCS-UHFFFAOYSA-N vat green 1 Chemical compound C1=CC=C[C]2C(=O)C(C3=C45)=CC=C4C(C4=C67)=CC=C7C(=O)[C]7C=CC=CC7=C6C=C(OC)C4=C5C(OC)=CC3=C21 JXUKQCUPTNLTCS-UHFFFAOYSA-N 0.000 description 1
- YKSGNOMLAIJTLT-UHFFFAOYSA-N violanthrone Chemical compound C12=C3C4=CC=C2C2=CC=CC=C2C(=O)C1=CC=C3C1=CC=C2C(=O)C3=CC=CC=C3C3=CC=C4C1=C32 YKSGNOMLAIJTLT-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Landscapes
- Coloring (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明はセルロース系繊維を含む染色物のソーピング剤
および染色物の処理法に関する。ざらに詳しくはセルロ
ース系繊維を含む繊維製品を反応性染料、ス!ノン染料
なとを含む染料で染邑した後未染着染料を除去するため
のソーピング剤J’3よび処理法に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a soaping agent for dyed articles containing cellulose fibers and a method for treating dyed articles. For more details, use reactive dyes to dye textile products containing cellulose fibers! This invention relates to a soaping agent J'3 and a treatment method for removing undyed dyes after dyeing with dyes including non-dyes.
[従来の技術]
従来セルロース系繊維染色物は高級アミンのエチレンオ
キサイド付加物、高級脂肪酸のソータ゛1h、高級脂肪
酸のエチレンオキサイトド1加物、ポリアクリル酸ソー
ダ塩などのソーピング剤を用い!′)0″C以上の水溶
液でソーピングないし洗?′fiを行っ゛イニいる。[Prior Art] Conventionally, cellulose fiber dyeing products use soaping agents such as ethylene oxide adducts of higher amines, sorter 1h of higher fatty acids, ethylene oxide 1 adducts of higher fatty acids, and sodium polyacrylate! ') Soap or wash with an aqueous solution of 0''C or higher.
[発明が解決しようとする問題点]
近年繊維製品の染色加工は省エネルギー、省ノ」化など
の合理化を余儀なくされ、たとえば70〜75℃の低温
度でソーピングないし洗浄することを要望されているが
、前記の従来のソーピング剤では90℃で行った場合の
ソーピング効果が1恥チれない。[Problems to be solved by the invention] In recent years, the dyeing process of textile products has been forced to be streamlined to save energy and reduce costs, and for example, there has been a demand for soaping or washing at a low temperature of 70 to 75 degrees Celsius. However, the conventional soaping agents described above have a comparable soaping effect when used at 90°C.
[問題点を解決するだめの手段]
本発明者らは上記セルロース系繊維を含む繊鉗染色物に
おいて、70〜75℃の低温度でソーピングないし洗浄
を行い90℃以上で行った場合と同じソーピング効果の
得られるソーピング剤および処理法を得るべく鋭意検討
した結果、本発明に到達した。[Means to Solve the Problem] The present inventors have carried out soaping or washing at a low temperature of 70 to 75°C, which is the same as when soaping or washing is carried out at a temperature of 90°C or higher, for the above-mentioned dyed products containing cellulose fibers. As a result of extensive research to find an effective soaping agent and treatment method, the present invention was achieved.
すなわち、本発明は重合脂肪酸の水溶性塩を含有するこ
とを特徴とするセルロース系wc維染色物用ソーピング
剤および重合脂肪酸の水溶性塩を少なくとも一種含有す
るソーピング剤を用いてソーピング浴のpHがIOから
12未満でセルロース系繊維染色物をソーピングするこ
とを特徴とするセルロース系繊維染色物の処理法である
。That is, the present invention uses a soaping agent for dyed cellulose WC fibers characterized by containing a water-soluble salt of a polymerized fatty acid, and a soaping agent containing at least one water-soluble salt of a polymerized fatty acid to adjust the pH of a soaping bath. A method for treating dyed cellulosic fibers, which comprises soaping the dyed cellulosic fibers at an IO of less than 12.
本発明における重合脂肪酸としては脂肪酸を重合して得
られる重合脂肪酸が挙げられる。Examples of the polymerized fatty acid in the present invention include polymerized fatty acids obtained by polymerizing fatty acids.
脂肪酸としては、炭素原子8〜24の天然または合成の
飽和脂肪酸、エチレン系不飽和脂肪酸およびアセチレン
系不飽和脂肪酸が挙げられる。Fatty acids include natural or synthetic saturated fatty acids, ethylenically unsaturated fatty acids, and acetylenically unsaturated fatty acids having 8 to 24 carbon atoms.
飽和脂肪酸、エチレン系不飽和脂肪酸およびアセチレン
系不飽和脂肪酸は、いくぶん違った方法で一般に重合で
きる。Saturated fatty acids, ethylenically unsaturated fatty acids and acetylenically unsaturated fatty acids can generally be polymerized in somewhat different ways.
飽和脂肪酸は重合が困難であるが重合は過酸化ジ−t−
ブチルのような過酸化物触媒を用い高温で行うことかて
ぎる。重金生成物の収量は一般に少ない。It is difficult to polymerize saturated fatty acids, but polymerization is possible with di-t-peroxide.
This can be done at high temperatures using peroxide catalysts such as butyl. Yields of heavy metal products are generally low.
適当な飽和脂肪酸どしては直鎮または分岐のもの、たと
えば゛カフプリル酸、ベラルコ′ン酸、カプリン酸、ラ
ウリン酸、ミリスチンΔな、バルミチン酸、イソパルミ
チン酸、スデアリン酸、アラギン酸、ベヘン酸および刀
グツセリン酸などが挙げられる。Suitable saturated fatty acids are straight or branched, such as cafprilic acid, belarconic acid, capric acid, lauric acid, myristic acid, valmitic acid, isopalmitic acid, suderic acid, aragic acid, behenic acid. and gutuceric acid.
エチレン系不飽和脂肪酸は容易に触媒または非触媒重合
法で重合できる。非触媒重合は一般に:′3゜O℃前後
の高温を要する。重合に適する触媒どしては酸性あるい
はアルカリ性粘土、過酸化ジー1.ブチル、3フツ化ホ
ウ素および曲のルイス酸、アンスラキノン、二酸化イオ
ウなとが挙げられる。Ethylenically unsaturated fatty acids can be easily polymerized by catalytic or non-catalytic polymerization methods. Non-catalytic polymerization generally requires high temperatures of around 3'3°C. Catalysts suitable for polymerization include acidic or alkaline clays, peroxide 1. Examples include butyl, boron trifluoride, Lewis acids, anthraquinone, sulfur dioxide, and the like.
適当なエチレン系不飽和脂肪酸としては、:゛(−オク
チン酸、ミリストオレイン酸、ツヅ酸、パルミI・−ル
酸、ペトロセリン酸、オレイン酸、エライジン酸、バク
セン酸、力下しン酸、セトレイン酸、ネルボン酸、リノ
ール酸、リル)酸、エレオステアリン酸、ヒラゴ酸、モ
ロクチ酸、/l、 )1.12゜15、18−エイコサ
ペンタエン酸、エイコサう2トラエン酸、ニシン酸、ヒ
ラガシラ酸およびショールムーブ刀−ン酸のような分岐
または直鎖のポリおよびモノエチレン系不飽和脂肪酸が
挙げられる。Suitable ethylenically unsaturated fatty acids include: ゛(-octic acid, myristoleic acid, tuzuic acid, palmic acid, petroselic acid, oleic acid, elaidic acid, vaccenic acid, phosphoric acid, Cetoleic acid, nervonic acid, linoleic acid, lylic acid, eleostearic acid, hiragic acid, moloctic acid, /l, )1.12゜15,18-eicosapentaenoic acid, eicosapentaenoic acid, nisic acid, Hiragashira Branched or straight chain poly and monoethylenically unsaturated fatty acids such as acids and Shoalmoon acids.
アセチレン系不飽和脂肪酸は単に加熱することにより重
合することができる。これらの反応性の高い物質の重合
は触媒なしで行うことができる。Acetylenically unsaturated fatty acids can be polymerized simply by heating. Polymerization of these highly reactive substances can be carried out without catalysts.
アセチレン系不飽和脂肪酸は天然には極めてまれにしか
存在しないから高価である。アセチレン系不飽和脂肪酸
としては、直鎖および分岐のモノ不飽和およびポリ不飽
和アセチレン系不飽和脂肪酸が挙げられ、これらの具体
例としては1o−ウンデシレン酸、タウリン酸、ステア
ロール酸、ベヘノール酸およびイサム酸がある。Acetylenically unsaturated fatty acids are extremely rare in nature and are therefore expensive. Acetylenically unsaturated fatty acids include linear and branched monounsaturated and polyunsaturated acetylenically unsaturated fatty acids, specific examples of which are 1o-undecylenic acid, tauric acid, stearolic acid, behenolic acid and There is isamic acid.
これらの脂肪酸のうち人手が容易で重合が比較的容易な
点で好ましいのはエチレン系不飽和脂肪酸でありオレイ
ン酸とリノール酸は重合脂肪酸の製造に適した出発物質
である。Among these fatty acids, ethylenically unsaturated fatty acids are preferred because they are easy to handle and relatively easy to polymerize, and oleic acid and linoleic acid are suitable starting materials for producing polymerized fatty acids.
上記のような重合脂肪酸またはその誘導体くたとえばエ
ステル)が(Hられたら、これを蒸留または溶媒抽出な
どの常法によって分留することができる。これらはさら
に水素添加触媒の存在下で水素圧を用いて不飽和を還元
し水素添加(蒸留前;1:たは後)することもできる。Once the polymerized fatty acids or their derivatives, such as esters, as described above have been hydrogenated, they can be fractionated by conventional methods such as distillation or solvent extraction. It can also be used to reduce unsaturation and hydrogenate (before; 1:1 or after).
C−18不飽和脂肪酸を基にした市販の重合脂肪酸の典
型的組成は、
C−18−塩基酸(単量体)0〜15重量%C−36二
塩基酸(二量体)60〜80重蚤%C−54(および以
上)多塩基酸(三量体)0〜35重蚤%
である。The typical composition of commercially available polymerized fatty acids based on C-18 unsaturated fatty acids is: 0-15% by weight C-18-basic acid (monomer) 60-80% C-36 dibasic acid (dimer) C-54 (and above) polybasic acid (trimer) 0-35% C-54.
具体的商品には、バーザダイム21G[モノマー酸8%
、ダイマー酸74%、トリマー酸18%、ヘン))”ル
白水(製)]、ババーサイイム228同 596、同7
(i%、同19%、ヘンケル白水(製)]、バーサシイ
ム288[同 2%、同 94%、同 4% ヘンケル
白水(製)]、ババーサイイム213同 2%、同 3
3%、同 65%、ヘンケル白水(製)コなどが挙げら
れる。Specific products include Verzadime 21G [monomer acid 8%
, Dimer acid 74%, Trimer acid 18%, Hen) "Le Hakusui (manufactured by)", Babasaiim 228 596, 7
(i%, 19%, Henkel Hakusui (manufactured)], Versathyim 288 [2%, 94%, 4% Henkel Hakusui (manufactured)], Babersyim 213 2%, 3
3%, 65%, and Henkel Hakusui Co., Ltd.
本発明における重合脂肪酸の水溶性」ttとしてはアル
カリ金属塩<−t−r−リウム、カリウノ1、リチウム
塩など)、アンモニウム塩およびアミン塩(メチルアミ
ン、ジメチルアミン、トリエチルアミン、モノエタノー
ルアミン、ジェタノールアミン、I・リエタノールアミ
ン塩など)が挙げられる。これらのうち好ましくは、ア
ルカリ金属塩でありとくに好ましくはナトリウムおよび
カリウノ、である。Examples of the water solubility of the polymerized fatty acids in the present invention include alkali metal salts <-t-r-lium, kaliuno-1, lithium salts, etc.), ammonium salts, and amine salts (methylamine, dimethylamine, triethylamine, monoethanolamine, tanolamine, I-liethanolamine salt, etc.). Among these, preferred are alkali metal salts, and particularly preferred are sodium and potassium salts.
塩は部分塩でも完全塩でもよいが完全塩が好ましい。The salt may be either a partial salt or a complete salt, but a complete salt is preferred.
この塩は重合脂肪酸を塩基性化合物で部分中和または完
全中和することによって容易に得られる。This salt can be easily obtained by partially or completely neutralizing the polymerized fatty acid with a basic compound.
塩基性化合物としては、水酸化すトリウム、水酸化カリ
ウム、水酸化リチウムなどのアルカリ金属水酸化物、メ
チルアミン、ジメチルアミン、トリエチルアミン、モノ
エタノールアミン、ジェタノールアミン、トリエタノー
ルアミンなどのアミン類;炭酸ナトリウム、炭酸カリウ
ム、炭酸リチリムなどのアルカリ金属炭酸塩などが挙げ
られる。Basic compounds include alkali metal hydroxides such as thorium hydroxide, potassium hydroxide, and lithium hydroxide; amines such as methylamine, dimethylamine, triethylamine, monoethanolamine, jetanolamine, and triethanolamine; Examples include alkali metal carbonates such as sodium carbonate, potassium carbonate, and lityrim carbonate.
重合脂肪酸の水溶性塩のうちで好ましいものは、ダイマ
ー酸すトリウム塩、ダイマー酸カリウム塩、トリマー酸
すトリウム塩、トリマー酸カリウム塩、ダイマー酸とト
リマー酸混合物のすトリウム塩J5よびダイマー酸とト
リマー酸混合物の力lハンム」hである。Among the water-soluble salts of polymerized fatty acids, preferred are storium salt of dimer acid, potassium salt of dimer acid, storium trimer acid salt, potassium salt of trimer acid, storium salt J5 of dimer acid and trimer acid mixture, and storium salt of dimer acid and trimer acid mixture. The power of the trimer acid mixture is ``h''.
本発明のソーピング剤を適用できるセルロ−ス系繊維以
外としては木綿、麻などのような天然繊ittおよびビ
スコースレーヨン、銅アンモニアレーヨンなどのような
再生繊維を挙げることができる。Examples of fibers other than cellulose fibers to which the soaping agent of the present invention can be applied include natural fibers such as cotton and linen, and recycled fibers such as viscose rayon and copper ammonia rayon.
また上記繊維と他の天然繊維(たとえば羊毛、絹)また
は合成N維(たとえばポリエステル/綿混、11クリア
ミド繊維、ポリアクリル繊維、アセテート繊維)などと
の混紡、交編織物でもよい。繊維形体としては、わた、
トつ、テープ、チーズ、ケーク、布 、緒糸なと何れで
も良い。It may also be a blended or interwoven fabric of the above fibers and other natural fibers (for example, wool, silk) or synthetic N fibers (for example, polyester/cotton blend, 11 clearamide fiber, polyacrylic fiber, acetate fiber). Examples of fibrous forms include cotton,
Thongs, tape, cheese, cake, cloth, threads, etc. are all fine.
これらの!a紺製品の染色にあたりセル【7−ス系繊維
のみであれば、反応性染料、ナフト−ル染料、硫化染お
[、スレン染料などの染料を用いることができる。一方
混紡、交編織物のセルロース系繊維以外の繊維を含む場
合の繊維の染色は酸性染料、含金属錯塩染料、反応性染
料、分散染料、カチオン染料などの染料を用いることが
できる。these! When dyeing navy blue products, if only cellulose fibers are used, dyes such as reactive dyes, naphthol dyes, sulfur dyes, and thren dyes can be used. On the other hand, dyes such as acid dyes, metal-containing complex salt dyes, reactive dyes, disperse dyes, and cationic dyes can be used to dye the fibers of blended and interwoven fabrics containing fibers other than cellulose fibers.
これらの染わ1を用いて繊維製品を染色する場合染色法
として一浴一段法(単一繊維)、−浴二段法(ポリエス
テル/綿混なと)および二浴二段法(−浴一段法または
一浴二段法では難しい混紡、交織品など)が挙げられる
。When dyeing textile products using these dyes 1, the dyeing methods are one-bath one-stage method (single fiber), two-bath two-stage method (polyester/cotton blend), and two-bath two-stage method (-one bath one-stage method). Examples include blended fabrics, interwoven fabrics, etc. that are difficult to produce using the one-bath or two-step process.
これらの染色はチーズ染色機、ドラム染色機、ウィンス
染色機、液流染色機を用いて常法で行うことができる。These dyeings can be carried out in a conventional manner using a cheese dyeing machine, a drum dyeing machine, a wince dyeing machine, or a jet dyeing machine.
このようにして′tA′:、邑された染色物は、ソーピ
ングに供される。ソーピングないし洗浄するに際し、本
発明のソーピング剤は必要により他の配合剤、たとえば
他のソーピング剤(アルギルフェノールのエチレンオキ
サイド付加物、高級アルコールのエチレンオキサイド付
加物、高級脂肪酸のエチレンオキサイド付加物、高級脂
肪酸とアルカノールアミンとのアミド化物、高級アミン
のエチレンオキサイド付加物、高級脂肪酸のアルカリ金
属塩、高級アルコールの硫酸エステル塩、ナフタレンス
ルホン酸ソーダのホルマリン縮合物、ポリアクリル酸ソ
ーダ、ポリビニルピロリドン、メチルカルボキシメチル
セルロースなど)およびアルカノールダー(苛性ソーダ
、炭酸ソーダ、トリポリリン酸ソーダなど)と併用する
ことができる。曲のソーピング剤の匝用量は全ソーピン
グ剤中、通常50重置火以下である。これらは、水溶液
j:た(、J:水分散液としソーピング浴または、洗浄
浴とする。The thus dyed product is subjected to soaping. When soaping or washing, the soaping agent of the present invention may be used, if necessary, with other compounding agents, such as other soaping agents (ethylene oxide adducts of argylphenol, ethylene oxide adducts of higher alcohols, ethylene oxide adducts of higher fatty acids, etc.). Amidated products of higher fatty acids and alkanolamines, ethylene oxide adducts of higher amines, alkali metal salts of higher fatty acids, sulfuric ester salts of higher alcohols, formalin condensates of sodium naphthalene sulfonate, sodium polyacrylate, polyvinylpyrrolidone, methyl carboxymethyl cellulose, etc.) and alkanolders (caustic soda, soda carbonate, sodium tripolyphosphate, etc.). Of all the soaping agents, the amount of soaping agents used is usually less than 50 times. These are an aqueous solution (J: aqueous dispersion) and a soaping bath or a washing bath.
本発明のソーピング剤(A)と他のソーピング剤(B)
を併用する場合、その併用方法は制限されない。Soaping agent (A) of the present invention and other soaping agents (B)
When used together, there are no restrictions on how they can be used together.
たとえば、(A)および(II)を予め混合し、浴(水
浴)中で(A)および(B)よりなるソーピング剤溶液
ヲ作成しても良い。また(A)お、1;び(II)をそ
のU善トtfたは水に溶解し両者を同時にまたは順次に
浴に添加する方法があげられる。For example, (A) and (II) may be mixed in advance to prepare a soaping agent solution consisting of (A) and (B) in a bath (water bath). Another method is to dissolve (A), (1), and (II) in the liquid or water and add both simultaneously or sequentially to the bath.
また、塩基性化合物の浴中に重合脂肪酸および/または
他のソーピング剤を添加して或はその逆の方法によって
本発明のソーピング剤を作成してもよい。The soaping agent of the present invention may also be prepared by adding polymerized fatty acids and/or other soaping agents to a basic compound bath, or vice versa.
ざらに塩基性化合物の浴中て先ず処理し、次いで別浴に
準備した重合脂肪酸および他のソーピング剤の浴で処理
してもよい。It is also possible to treat the raw material first in a bath of a basic compound and then in a bath of polymerized fatty acids and other soaping agents prepared in a separate bath.
浴中の全ソーピング剤の濃度こ;を通常0.2〜7g/
l、好ましくは0.4〜52./l(固形分)である。The concentration of total soaping agent in the bath is usually 0.2 to 7 g/
l, preferably 0.4 to 52. /l (solid content).
またアルカリビルグーを使用する場合、その濃度は、通
常O〜10g/I、好ましくは0〜5g/lである。When alkaline bilgu is used, its concentration is usually 0 to 10 g/l, preferably 0 to 5 g/l.
ソーピング浴の1〕1(は通常10から12未満であり
、好ましくは、10.5〜11.8である。pl+が1
0未)^1の場合は繊維上の未染着染料の脱落、除去効
果が乏しくなる。また12を越えると染色物の変色が大
きく、色相の再現性に欠ける。1]1 (of the soaping bath is usually from 10 to less than 12, preferably from 10.5 to 11.8. pl+ is 1
In the case of 1), the effect of shedding and removing undyed dyes on the fibers becomes poor. Moreover, if it exceeds 12, the dyed product will be greatly discolored and the reproducibility of the hue will be lacking.
本発明のソーピングは通常70〜75℃の温度で行うが
、勿論、従来の1〕0℃以上で行ってもよく、この場合
は当然従来のソーピング法(ソーピング剤)に比べれば
数段ソーピング効果にすぐれることは言うまでもない。The soaping of the present invention is usually carried out at a temperature of 70 to 75 degrees Celsius, but of course it may also be carried out at a temperature of 1] 0 degrees Celsius or higher, which is naturally more effective than the conventional soaping method (soaping agent). Needless to say, it is excellent.
本発明のソーピング剤は液?R染色機、ウィンスおよび
他の染色機のいずれて染色された染色物のソーピングに
対しても使用することができるが、たとえば、液流染色
機で染色された染色物を染色機外へ取り出すことなく継
続してソーピングするのが好ましい。Is the soaping agent of the present invention a liquid? It can also be used for soaping dyed products dyed with R dyeing machines, Wince and other dyeing machines, but for example, it can be used to take out dyed products dyed with jet dyeing machines out of the dyeing machine. It is preferable to soap continuously.
液流染色機を用いてソーピングする場合、通常染色後染
色物を含む染色?(’2を排除、水洗し本発明のソーピ
ング浴を染色機中に形成させ、染色機を運転してソーピ
ングないし洗)争する。この場合の条件は通常下記のと
おりである。When soaping using a jet dyeing machine, does it usually include dyeing after dyeing? (Excluding '2, washing with water, forming the soaping bath of the present invention in the dyeing machine, operating the dyeing machine for soaping or washing). The conditions in this case are usually as follows.
即ち、布速(n+/分)は60〜150、染色回転数(
回/分)1.5〜3、浴比は1:10〜20、昇温時間
(分)は15〜25、温度(’C) 20〜75℃(実
質のソーピング温度は70〜75℃)総ソーピング所要
時間(分)は、25〜50である。ソーピング後の染色
物は、水洗、乾燥される。That is, the cloth speed (n+/min) is 60 to 150, and the dyeing rotation number (
times/min) 1.5-3, bath ratio 1:10-20, heating time (min) 15-25, temperature ('C) 20-75℃ (actual soaping temperature 70-75℃) The total soaping time (minutes) is 25-50 minutes. After soaping, the dyed product is washed with water and dried.
本発明のソーピング剤は従来の染色(熾(r二r″:l
((“1、ウィンスなど)やオープンソーパーでも防用
できる。The soaping agent of the present invention is suitable for conventional dyeing (熾(r2r″:l
((“1, Wince, etc.)” and open soaper can also be used for defense.
[実施例]
以下に実施例および試験例により本発明をざらに説明す
るが、本発明は、これに限定されるものではない。[Examples] The present invention will be briefly described below with reference to Examples and Test Examples, but the present invention is not limited thereto.
実施例 1−4、比中々例 1〜3 本発明のソーピング剤および比較品を示す。Examples 1-4, Specific examples 1-3 The soaping agent of the present invention and a comparative product are shown.
実施例 1:バーサジイム216ナトリウム塩実施例
2:バーサダイム228すトリウム塩実施例 3:バー
サグイム288カリウム塩実施例 4:バーサグイム2
13カリウム塩比較例 1ニオレイン酸のエチレンオギ
ザイド付加物(14モル)
比較例 2ニステアリン酸ナトリウム
比較例 3:ポリアクリル酸すl・リウム(分子量:1
0000)
試験例1
(白湯汚染性試験)
本発明のソーピング剤(実施例1〜4)及び比較品(比
較例1〜3)を用いソーピング浴を作成し、該浴に各染
色布5gと未染色のマルチファイバー・テストクロス5
gを投入し下記条件でソーピングしたマルチファイバー
・テスI・クロスの各繊維部の汚染程度をグレースゲー
ルにて判定しその結果を表1〜9に示した。Example 1: Versadime 216 Sodium Salt Example
2: Versadigm 228 thorium salt example 3: Versagym 288 potassium salt example 4: Versagym 2
13 Potassium salt comparative example 1 Ethylene ogizide adduct of nioleic acid (14 mol) Comparative example 2 Sodium stearate comparative example 3: Polyacrylate sulfur and lithium (molecular weight: 1
0000) Test Example 1 (White water staining test) A soaping bath was prepared using the soaping agent of the present invention (Examples 1 to 4) and comparative products (Comparative Examples 1 to 3), and 5 g of each dyed cloth and untreated cloth were added to the bath. Dyeing multi-fiber test cloth 5
The degree of contamination of each fiber part of the multi-fiber Tes I cloth which was soaped under the following conditions using Grace Gale was determined and the results are shown in Tables 1 to 9.
[試験条件]
1)試 布:綿メリヤス(精練漂白済み)マルチファイ
バー・テストクロス
(添1寸イ11)
2)染色条件二次のそれぞれの染料の一般染色処方にし
たがって染色した。[Test Conditions] 1) Sample fabric: Cotton knitted (scoured and bleached) multi-fiber test cloth (attached 1 dimension A 11) 2) Dyeing conditions Dyeing was carried out according to the general dyeing recipe for each of the secondary dyes.
染料
a、c、1.Reactive Red 21
5:E o、sy、f。Dyes a, c, 1. Reactive Red 21
5: E o, sy, f.
b、c、1.ReacLive Blue 21
5Z o、−y、f。b, c, 1. ReacLive Blue 21
5Z o, -y, f.
c、c、1.Reactive [31ack
5 5’f:、 o、sy、f。c, c, 1. Reactive [31ack
5 5'f:, o, sy, f.
d、c、1.5ulphur Red 13
15χ o、sy、f’。d, c, 1.5ulphur Red 13
15χ o, sy, f'.
e、(,1,5ull由ur Black
l 20χ o、sy、f。e, (,1,5ull ur Black
l 20χ o, sy, f.
f、c、1.Vat Blue 20 6
%: o、ty、f。f, c, 1. Vat Blue 20 6
%: o, ty, f.
g、c、1.Vat Green 1 6
% (川y、f。g, c, 1. Vat Green 1 6
% (kawa y, f.
h、c、1.A、D、c、(salt、) 3
153/1i、c、1.A、D、c、(salt)
20 15g/13)ソーピング浴
ソーピング剤 0.6g/l (ViI形分)苛性ソ
ーダ 0.1g/! (固形分)浴比
1:lO
温度、時間 70℃Xl0分、90℃X1O分水洗
20℃×3分
乾燥 105℃×30分
4)試験機
振とう式染色機[辻井染機((3)製]試j倹例2
(ソーピング試験)
本発明のソーピング剤(実施例1〜4)および比較品(
比較例1〜3)を用い試験例1と同じソーピング浴を作
成し該浴に各染色布10gを投入し試験例1と同条件で
ソーピングした。各ソーピング布について下記の染色堅
牢度試験を行いその結果を表10〜18に示した。h, c, 1. A, D, c, (salt,) 3
153/1i, c, 1. A, D, c, (salt)
20 15g/13) Soaping bath Soaping agent 0.6g/l (ViI type) Caustic soda 0.1g/! (solid content) bath ratio
1:1O Temperature, time 70°C x 10 minutes, 90°C x 10 minutes Washing 20°C x 3 minutes Drying 105°C x 30 minutes 4) Testing machine Shaking dyeing machine [Tsujii dyeing machine (manufactured by (3)]) Trial example 2 (Soaping test) The soaping agent of the present invention (Examples 1 to 4) and the comparative product (
Comparative Examples 1 to 3) were used to prepare the same soaping bath as in Test Example 1, and 10 g of each dyed fabric was placed in the bath and soaped under the same conditions as in Test Example 1. Each soaping cloth was subjected to the following color fastness test and the results are shown in Tables 10 to 18.
1)洗濯堅牢度試験
JIS LO844A−4号法、試験後の添付布の汚
染をグレースケールにて判定した。(級)
2)水堅牢度試験
JIS !、0846 [3法(16時間)試験後
の添付布の汚染をグルースケールにて判定した。(級)
3)汗堅牢度試験
JIS 10848 A法、酸、アルカリ試験後の
添付布の汚染をグレースケールにて判定した。(級)4
)摩擦堅牢度試験
JIS LO849乾式および湿式摩擦試験[QTI
型にて200gの荷重100回往1豆摩擦後添付布の汚
染をグレースケールにで判定した。(級)
試験例3
(起泡性試験)
本発明のソーピング剤(実施例1〜4)および比jli
S′″品(比較例1〜3)を用い試験例1と同じソーピ
ング浴を作成し起泡性試験機にて起泡量(1皿)を測定
しその結果を表19に示した。1) Washing fastness test JIS LO844A-4 method, contamination of the attached fabric after the test was determined on a gray scale. (Grade) 2) Water fastness test JIS! , 0846 [The contamination of the attached cloth after the 3-method (16 hour) test was determined using a glue scale. (class)
3) Sweat fastness test JIS 10848 A method, acid and alkali tests were conducted to determine the contamination of the attached cloth using gray scale. (grade) 4
) Abrasion fastness test JIS LO849 dry and wet abrasion test [QTI
After rubbing with a mold 100 times under a load of 200 g, the contamination of the attached cloth was determined on a gray scale. (grade) Test Example 3 (Foaming property test) Soaping agents of the present invention (Examples 1 to 4) and ratio jli
The same soaping bath as in Test Example 1 was prepared using S''' products (Comparative Examples 1 to 3), and the foaming amount (one dish) was measured using a foaming tester. The results are shown in Table 19.
(試験条件)
液量 : 1.5+
循環液量 : 1.5+/分
ノズル径 :1印
試験機 :噴射式液流起泡性試験機
[発明の効果コ
ト0本発明のソー・ピング剤はセルロース系繊維を含む
繊維染色物において70〜75℃の低温度でソーピング
ないし洗浄を行い90℃以上で行った場合と同じソーピ
ング効果が得られる。すなわち白湯の汚染が少なく、ま
た鮮明かつ洗たく、水、汗、摩擦などの染色堅牢度にす
ぐれる染色物を得ることができる。(Test conditions) Liquid amount: 1.5+ Circulating liquid amount: 1.5+/min Nozzle diameter: 1 mark Testing machine: Injection type liquid flow foaming tester [Effects of the invention 0 The sawing agent of the present invention When soaping or washing dyed fibers containing cellulose fibers at a low temperature of 70 to 75°C, the same soaping effect as when carried out at 90°C or higher can be obtained. In other words, it is possible to obtain a dyed product with less contamination of hot water, clear color, easy to wash, and excellent color fastness against water, sweat, friction, etc.
2、また本発明のソーピング剤は、高級脂肪酸のソーダ
塩、高級脂肪酸のエチレンオキサイド付加物、高級アル
コールのエチレンオキサイド付加物などの従来のソーピ
ング剤に比べて起泡性が少なく、ラビッド?iX流染色
債ても使用可能である。2. Also, the soaping agent of the present invention has less foaming properties than conventional soaping agents such as soda salts of higher fatty acids, ethylene oxide adducts of higher fatty acids, and ethylene oxide adducts of higher alcohols. iX dye bond can also be used.
3、本発明のソーピング剤は通常の高級脂肪酸のソーダ
塩のように用水中のカルシウム及びマグネシウムイオン
と結合し水不溶性のアルカリ金属塩となって染色布に白
粉やスペックなどの汚染を引き起こすことがない。3. The soaping agent of the present invention, like ordinary soda salts of higher fatty acids, does not combine with calcium and magnesium ions in water to form water-insoluble alkali metal salts, causing stains such as white powder and speck on dyed fabrics. do not have.
Claims (1)
セルロース系繊維染色物用ソーピング剤。 2、セルロース系繊維染色物が反応性染料染色物である
請求項1記載のソーピング剤。 3、重合脂肪酸の水溶性塩を少なくとも一種含有するソ
ーピング剤を用いてソーピング浴のpHが10〜12未
満でセルロース系繊維染色物をソーピングすることを特
徴とするセルロース系繊維染色物の処理法。 4、ソーピングを75℃以下で行う請求項3記載の処理
法。[Scope of Claims] 1. A soaping agent for dyed cellulose fibers, which contains a water-soluble salt of a polymerized fatty acid. 2. The soaping agent according to claim 1, wherein the cellulosic fiber dyeing is a reactive dye dyeing. 3. A method for treating dyed cellulose fibers, which comprises soaping the dyed cellulose fibers at a pH of 10 to less than 12 in a soaping bath using a soaping agent containing at least one water-soluble salt of a polymerized fatty acid. 4. The treatment method according to claim 3, wherein the soaping is carried out at a temperature of 75°C or lower.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63101597A JPH01272888A (en) | 1988-04-25 | 1988-04-25 | Soaping agent and treatment using the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63101597A JPH01272888A (en) | 1988-04-25 | 1988-04-25 | Soaping agent and treatment using the same |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01272888A true JPH01272888A (en) | 1989-10-31 |
Family
ID=14304794
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63101597A Pending JPH01272888A (en) | 1988-04-25 | 1988-04-25 | Soaping agent and treatment using the same |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01272888A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006193852A (en) * | 2005-01-13 | 2006-07-27 | Nicca Chemical Co Ltd | Method for soaping reactive dye-dyed product |
-
1988
- 1988-04-25 JP JP63101597A patent/JPH01272888A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006193852A (en) * | 2005-01-13 | 2006-07-27 | Nicca Chemical Co Ltd | Method for soaping reactive dye-dyed product |
JP4627438B2 (en) * | 2005-01-13 | 2011-02-09 | 日華化学株式会社 | Soaping method for reactive dyes |
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