CN1336947A - 纤维活性偶氮染料的深黑染料混合物及使含羟基和/或酰胺基纤维染色的方法 - Google Patents
纤维活性偶氮染料的深黑染料混合物及使含羟基和/或酰胺基纤维染色的方法 Download PDFInfo
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- CN1336947A CN1336947A CN00802863A CN00802863A CN1336947A CN 1336947 A CN1336947 A CN 1336947A CN 00802863 A CN00802863 A CN 00802863A CN 00802863 A CN00802863 A CN 00802863A CN 1336947 A CN1336947 A CN 1336947A
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- dye mixture
- hydrogen
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- ethyl
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- 239000000975 dye Substances 0.000 title claims abstract description 192
- 239000000203 mixture Substances 0.000 title claims abstract description 109
- 238000004043 dyeing Methods 0.000 title claims abstract description 36
- 239000000835 fiber Substances 0.000 title claims abstract description 25
- 238000000034 method Methods 0.000 title claims description 31
- 125000002887 hydroxy group Chemical group [H]O* 0.000 title claims description 9
- 125000005518 carboxamido group Chemical group 0.000 title abstract 2
- 230000008569 process Effects 0.000 title description 8
- 239000000987 azo dye Substances 0.000 title description 2
- -1 amino-substituted chlorotriazinylamino-sulfo-naphthol Chemical class 0.000 claims abstract description 33
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims abstract description 13
- 239000001257 hydrogen Substances 0.000 claims description 37
- 229910052739 hydrogen Inorganic materials 0.000 claims description 37
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 26
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 26
- 239000000463 material Substances 0.000 claims description 25
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 19
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 15
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 15
- 150000002431 hydrogen Chemical class 0.000 claims description 15
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 15
- 238000000576 coating method Methods 0.000 claims description 12
- 239000011248 coating agent Substances 0.000 claims description 11
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 11
- 229920002554 vinyl polymer Polymers 0.000 claims description 11
- 239000003513 alkali Substances 0.000 claims description 9
- 125000003368 amide group Chemical group 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 229910019142 PO4 Inorganic materials 0.000 claims description 5
- 229910052728 basic metal Chemical group 0.000 claims description 5
- JMANVNJQNLATNU-UHFFFAOYSA-N glycolonitrile Natural products N#CC#N JMANVNJQNLATNU-UHFFFAOYSA-N 0.000 claims description 5
- 239000010452 phosphate Substances 0.000 claims description 5
- 150000003818 basic metals Chemical group 0.000 claims description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- 239000005864 Sulphur Substances 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
- 230000000694 effects Effects 0.000 claims description 2
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 claims 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims 1
- 238000005859 coupling reaction Methods 0.000 abstract description 23
- 210000002268 wool Anatomy 0.000 abstract description 18
- 230000008878 coupling Effects 0.000 abstract description 13
- 238000010168 coupling process Methods 0.000 abstract description 13
- 239000002657 fibrous material Substances 0.000 abstract description 10
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 abstract description 3
- 229920003043 Cellulose fiber Polymers 0.000 abstract description 2
- 229920000742 Cotton Polymers 0.000 abstract description 2
- 150000001448 anilines Chemical class 0.000 abstract 2
- AFOSIXZFDONLBT-UHFFFAOYSA-N divinyl sulfone Chemical class C=CS(=O)(=O)C=C AFOSIXZFDONLBT-UHFFFAOYSA-N 0.000 abstract 2
- APRRQJCCBSJQOQ-UHFFFAOYSA-N 4-amino-5-hydroxynaphthalene-2,7-disulfonic acid Chemical compound OS(=O)(=O)C1=CC(O)=C2C(N)=CC(S(O)(=O)=O)=CC2=C1 APRRQJCCBSJQOQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000004952 Polyamide Substances 0.000 abstract 1
- 229920002647 polyamide Polymers 0.000 abstract 1
- 125000006125 ethylsulfonyl group Chemical group 0.000 description 71
- 239000000243 solution Substances 0.000 description 32
- 239000002253 acid Substances 0.000 description 23
- 239000002585 base Substances 0.000 description 22
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- 239000007864 aqueous solution Substances 0.000 description 17
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 15
- 238000006243 chemical reaction Methods 0.000 description 14
- 238000007639 printing Methods 0.000 description 14
- 239000000985 reactive dye Substances 0.000 description 14
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 12
- 239000007788 liquid Substances 0.000 description 12
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 12
- 239000002932 luster Substances 0.000 description 11
- 238000002360 preparation method Methods 0.000 description 11
- 239000003795 chemical substances by application Substances 0.000 description 10
- 238000006193 diazotization reaction Methods 0.000 description 9
- 235000017550 sodium carbonate Nutrition 0.000 description 9
- 229910000029 sodium carbonate Inorganic materials 0.000 description 9
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 8
- 239000000843 powder Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- 235000017557 sodium bicarbonate Nutrition 0.000 description 7
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 6
- 239000003929 acidic solution Substances 0.000 description 6
- 150000001805 chlorine compounds Chemical class 0.000 description 6
- 235000010288 sodium nitrite Nutrition 0.000 description 6
- 238000001694 spray drying Methods 0.000 description 6
- 239000000725 suspension Substances 0.000 description 6
- KYARBIJYVGJZLB-UHFFFAOYSA-N 7-amino-4-hydroxy-2-naphthalenesulfonic acid Chemical class OC1=CC(S(O)(=O)=O)=CC2=CC(N)=CC=C21 KYARBIJYVGJZLB-UHFFFAOYSA-N 0.000 description 5
- 239000011230 binding agent Substances 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- 239000012064 sodium phosphate buffer Substances 0.000 description 5
- 238000010186 staining Methods 0.000 description 5
- 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 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 230000001105 regulatory effect Effects 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- WYRSGXAIHNMKOL-UHFFFAOYSA-N $l^{1}-sulfanylethane Chemical compound CC[S] WYRSGXAIHNMKOL-UHFFFAOYSA-N 0.000 description 3
- MFSFSFGGYUPAKQ-UHFFFAOYSA-N 1-amino-4-hydroxynaphthalene-2-sulfonic acid Chemical compound C1=CC=C2C(N)=C(S(O)(=O)=O)C=C(O)C2=C1 MFSFSFGGYUPAKQ-UHFFFAOYSA-N 0.000 description 3
- HIVUAOXLSJITPA-UHFFFAOYSA-N 2-amino-5-hydroxynaphthalene-1,7-disulfonic acid Chemical compound OC1=CC(S(O)(=O)=O)=CC2=C(S(O)(=O)=O)C(N)=CC=C21 HIVUAOXLSJITPA-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- DPDMMXDBJGCCQC-UHFFFAOYSA-N [Na].[Cl] Chemical compound [Na].[Cl] DPDMMXDBJGCCQC-UHFFFAOYSA-N 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 125000002252 acyl group Chemical group 0.000 description 3
- 239000012752 auxiliary agent Substances 0.000 description 3
- 239000000872 buffer Substances 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- 238000006467 substitution reaction Methods 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 2
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 150000001912 cyanamides Chemical class 0.000 description 2
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 2
- 229910000397 disodium phosphate Inorganic materials 0.000 description 2
- 235000019800 disodium phosphate Nutrition 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 230000000215 hyperchromic effect Effects 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 229940045641 monobasic sodium phosphate Drugs 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 239000001632 sodium acetate Substances 0.000 description 2
- 235000017281 sodium acetate Nutrition 0.000 description 2
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 description 1
- JBIJLHTVPXGSAM-UHFFFAOYSA-N 2-naphthylamine Chemical compound C1=CC=CC2=CC(N)=CC=C21 JBIJLHTVPXGSAM-UHFFFAOYSA-N 0.000 description 1
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 1
- 239000005695 Ammonium acetate Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical group C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 244000175448 Citrus madurensis Species 0.000 description 1
- 240000000491 Corchorus aestuans Species 0.000 description 1
- 235000011777 Corchorus aestuans Nutrition 0.000 description 1
- 235000010862 Corchorus capsularis Nutrition 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 229920000571 Nylon 11 Polymers 0.000 description 1
- 229920001007 Nylon 4 Polymers 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001339 alkali metal compounds Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 235000019257 ammonium acetate Nutrition 0.000 description 1
- 229940043376 ammonium acetate Drugs 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- CYGKLLHTPPFPHH-UHFFFAOYSA-N aniline;hydrate Chemical compound O.NC1=CC=CC=C1 CYGKLLHTPPFPHH-UHFFFAOYSA-N 0.000 description 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 238000003287 bathing Methods 0.000 description 1
- BEHLMOQXOSLGHN-UHFFFAOYSA-N benzenamine sulfate Chemical compound OS(=O)(=O)NC1=CC=CC=C1 BEHLMOQXOSLGHN-UHFFFAOYSA-N 0.000 description 1
- 229960003328 benzoyl peroxide Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 239000012954 diazonium Substances 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-O diazynium Chemical compound [NH+]#N IJGRMHOSHXDMSA-UHFFFAOYSA-O 0.000 description 1
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 159000000011 group IA salts Chemical class 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000009980 pad dyeing Methods 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- HLBBKKJFGFRGMU-UHFFFAOYSA-M sodium formate Chemical compound [Na+].[O-]C=O HLBBKKJFGFRGMU-UHFFFAOYSA-M 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000000979 synthetic dye Substances 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0033—Blends of pigments; Mixtured crystals; Solid solutions
- C09B67/0046—Mixtures of two or more azo dyes
- C09B67/0047—Mixtures of two or more reactive azo dyes
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/02—Material containing basic nitrogen
- D06P3/04—Material containing basic nitrogen containing amide groups
- D06P3/10—Material containing basic nitrogen containing amide groups using reactive dyes
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/58—Material containing hydroxyl groups
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Coloring (AREA)
Abstract
Description
例 | 基(4) | 基(5) | 基(6) | 比例(1)∶(2)∶(3) |
8 | 2-甲氧基-5-(β-硫酸根合乙基磺酰基)-苯基 | 4-(β-硫酸根合乙基磺酰基)-苯基 | 2-磺基-4-(β-硫酸根合乙基磺酰基)-苯基 | 85∶15∶0 |
9 | 2-磺基-4-(β-硫酸根合乙基磺酰基)-苯基 | 4-(β-硫酸根合乙基磺酰基)-苯基 | 4-(β-硫酸根合-乙基磺酰基)-苯基 | 85∶14∶1 |
10 | 2-羧基-4-(β-硫酸根合乙基磺酰基)-苯基 | 同上 | 同上 | 80∶19∶1 |
11 | 2-甲氧基-5-甲基-4-(β-硫酸根合乙基磺酰基)-苯基 | 同上 | 同上 | 80∶19∶1 |
12 | 2,5-二甲氧基-4-(β-硫酸根合乙基-磺酰基)-苯基 | 同上 | 同上 | 90∶10∶0 |
13 | 4-(β-硫酸根合乙基磺酰基)-苯基 | 3-(β-硫酸根合乙基磺酰基)-苯基 | 3-(β-硫酸根合-乙基磺酰基)-苯基 | 87∶12∶1 |
14 | 2-磺基-4-(β-硫酸根合乙基磺酰基)-苯基 | 4-(β-硫酸根合-乙基磺酰基)-苯基 | 2-甲氧基-5-(β-硫酸根合乙基-磺酰基)-苯基 | 89∶11∶0 |
15 | 同上 | 同上 | 2-甲氧基-5-甲基4-(β-硫酸根合乙基磺酰基)-苯基 | 75∶25∶0 |
16 | 同上 | 同上 | 3-(β-硫酸根合乙基磺酰基)-苯基 | 82∶18∶0 |
17 | 4-(β-硫酸根合乙基磺酰基)-苯基 | 同上 | 2-磺基-4-(β-硫酸根合乙基磺酰基)-苯基 | 88∶12∶0 |
18 | 2-甲氧基-5-(β-硫酸根合乙基磺酰基)-苯基 | 同上 | 2-羧基-4-(β-硫酸根合乙基磺酰基)-苯基 | 80∶20∶0 |
19 | 4-(β-硫酸根合乙基磺酰基)-苯基 | 同上 | 4-(β-硫酸根合乙基磺酰基)-苯基 | 77∶22.5∶0.5 |
例 | 基(4) | 基(5) | 基(6) | 比例(1)∶(2)∶(3) |
20 | 2-甲氧基-5-(β-硫酸根合乙基磺酰基)-苯基 | 4-(β-硫酸根合-乙基磺酰基)-苯基 | 2-磺基-4-(β-硫酸根合乙基磺酰基)-苯基 | 85∶15∶0 |
21 | 2-磺基-4-(β-硫酸根合乙基磺酰基)-苯基 | 4-(β-硫酸根合-乙基磺酰基)-苯基 | 4-(β-硫酸根合-乙基磺酰基)-苯基 | 85∶14∶1 |
22 | 2-羧基-4-(β-硫酸根合乙基磺酰基)-苯基 | 同上 | 同上 | 80∶19∶1 |
23 | 2-甲氧基-5-甲基-4-(β-硫酸根合乙基磺酰基)-苯基 | 同上 | 同上 | 80∶19∶1 |
24 | 2,5-二甲氧基-4-(β-硫酸根合乙基-磺酰基)-苯基 | 同上 | 同上 | 90∶10∶0 |
25 | 4-(β-硫酸根合乙基磺酰基)-苯基 | 3-(β-硫酸根合-乙基磺酰基)-苯基 | 3-(β-硫酸根合-乙基磺酰基)-苯基 | 87∶12∶1 |
26 | 2-磺基-4-(β-硫酸根合乙基磺酰基)-苯基 | 4-(β-硫酸根合-乙基磺酰基)-苯基 | 2-甲氧基-5-(β-硫酸根合乙基-磺酰基)-苯基 | 89∶11∶0 |
27 | 同上 | 同上 | 2-甲氧基-5-甲基-4-(β-硫酸根合乙基磺酰基)-苯基 | 75∶25∶0 |
28 | 同上 | 同上 | 3-(β-硫酸根合乙基磺酰基)-苯基 | 82∶18∶0 |
29 | 4-(β-硫酸根合乙基磺酰基)-苯基 | 同上 | 2-磺基-4-(β-硫酸根合乙基磺酰基)-苯基 | 88∶12∶0 |
30 | 2-甲氧基-5-(β-硫酸根合乙基磺酰基)-苯基 | 同上 | 2-羧基-4-(β-硫酸根合乙基磺酰基)-苯基 | 80∶20∶0 |
31 | 4-(β-硫酸根合乙基磺酰基)-苯基 | 同上 | 4-(β-硫酸根合乙基磺酰基)-苯基 | 77∶22.5∶0.5 |
Claims (13)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US09/249,756 US6015439A (en) | 1999-02-16 | 1999-02-16 | Deep black dye mixtures of fiber-reactive azo dyes and a process for dyeing hydroxy and/or carboxamido containing fibers |
US09/249,756 | 1999-02-16 |
Publications (2)
Publication Number | Publication Date |
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CN1336947A true CN1336947A (zh) | 2002-02-20 |
CN1120864C CN1120864C (zh) | 2003-09-10 |
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CN00802863A Expired - Lifetime CN1120864C (zh) | 1999-02-16 | 2000-02-09 | 纤维活性偶氮染料的深黑染料混合物及使含羟基和/或酰胺基纤维染色的方法 |
Country Status (9)
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US (1) | US6015439A (zh) |
EP (1) | EP1155089B1 (zh) |
JP (1) | JP4535415B2 (zh) |
KR (1) | KR100607566B1 (zh) |
CN (1) | CN1120864C (zh) |
AU (1) | AU2803300A (zh) |
DE (1) | DE60001152T2 (zh) |
TR (1) | TR200102353T2 (zh) |
WO (1) | WO2000049093A1 (zh) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2005058875A1 (fr) * | 2003-12-19 | 2005-06-30 | Shanghai Institute Of Materia Medica, Chinese Academy Of Sciences | Composes de piperazine triazine, leur obtention, et preparations pharmaceutiques les contenant |
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Publication number | Priority date | Publication date | Assignee | Title |
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US6051037A (en) * | 1999-04-21 | 2000-04-18 | Dystar Textil Farben Gmbh & Co. Deutschland Kg | Dye mixtures of fiber-reactive azo dyes and use thereof for dyeing material containing hydroxy- and/or carboxamido groups |
TR200103614T2 (tr) | 1999-06-24 | 2002-04-22 | Dystar Textilfarben Gmbh & Co. Deutschland Kg. | Reaktif boya karışımları |
TWI260334B (en) * | 1999-11-01 | 2006-08-21 | Clariant Int Ltd | Azo dyestuffs |
KR100357475B1 (ko) * | 2000-07-07 | 2002-10-18 | (주)경인양행 | 반응성 흑색 염료 조성물 |
KR100843102B1 (ko) * | 2006-05-11 | 2008-07-02 | (주)경인양행 | 반응성 염료 조성물 및 이를 이용한 섬유의 염색방법 |
CN100528972C (zh) * | 2006-08-18 | 2009-08-19 | 浙江龙盛集团股份有限公司 | 一种复合活性染料 |
JP5165880B2 (ja) * | 2006-11-06 | 2013-03-21 | ユニチカトレーディング株式会社 | 涼感性獣毛繊維布帛及びそれを用いてなるフォーマル衣料 |
CN101469138A (zh) * | 2007-12-24 | 2009-07-01 | 深圳泛胜塑胶助剂有限公司 | 稳定性高浓度液体活性染料混合物 |
CN103013176B (zh) * | 2013-01-05 | 2014-12-10 | 江苏德美科化工有限公司 | 一种高性能绿色活性染料混合物及其应用 |
EP2862902A1 (en) * | 2013-08-29 | 2015-04-22 | DyStar Colours Distribution GmbH | Dye mixtures of metal free reactive dyes, production and use |
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JPS63178170A (ja) * | 1987-01-16 | 1988-07-22 | Sumitomo Chem Co Ltd | 反応染料組成物およびセルロ−ス系繊維材料の染色または捺染方法 |
JP2631006B2 (ja) * | 1988-03-24 | 1997-07-16 | ダイスタージャパン株式会社 | 黒色用反応染料混合物 |
JPH0774314B2 (ja) * | 1988-09-08 | 1995-08-09 | 三菱化学株式会社 | 水溶性染料混合物 |
JPH02202956A (ja) * | 1989-01-24 | 1990-08-13 | Rika Sangyo Kk | 反応性黒色染料組成物 |
BR9007355A (pt) * | 1989-05-10 | 1992-04-28 | Hoechst Ag | Corantes azoicos soluveis em agua,processo para a sua obtencao e sua aplicacao |
KR910008343A (ko) * | 1989-10-13 | 1991-05-31 | 김한중 | Lpg, lng 가스를 연료로 한 공기보일러 및 알미늄샷시를 재료로한 온돌 공기 장판 |
TW223653B (zh) * | 1991-05-11 | 1994-05-11 | Hoechst Ag | |
JPH0797533A (ja) * | 1993-08-02 | 1995-04-11 | Mitsubishi Kasei Hoechst Kk | 水溶性染料混合物及びセルロース系繊維材料の染色又は捺染法 |
DE4414320A1 (de) * | 1994-04-25 | 1995-10-26 | Hoechst Ag | Schwarze Farbstoffmischungen von faserreaktiven Azofarbstoffen und ihre Verwendung zum Färben von hydroxy- und/oder carbonamidgruppenhaltigem Fasermaterial |
JPH07324172A (ja) * | 1994-05-31 | 1995-12-12 | Mitsubishi Kasei Hoechst Kk | 水溶性染料混合物及びセルロース繊維材料の染色又は捺染法 |
JP3817765B2 (ja) * | 1995-12-19 | 2006-09-06 | 住友化学株式会社 | 反応染料組成物およびそれを用いる染色または捺染法 |
JP3915131B2 (ja) * | 1995-12-19 | 2007-05-16 | 住友化学株式会社 | 反応染料の液状水性組成物およびそれを用いる染色または捺染法 |
DE19635999A1 (de) * | 1996-09-05 | 1998-03-12 | Dystar Textilfarben Gmbh & Co | Farbstoffmischungen von faserreaktiven Azofarbstoffen und ihre Verwendung zum Färben von hydroxy- und/oder carbonamidgruppenhaltigem Fasermaterial |
KR19990025263A (ko) * | 1997-09-11 | 1999-04-06 | 양재신 | 연료 탱크 주유성 시험 장치 |
US5931976A (en) * | 1998-08-11 | 1999-08-03 | Dystar Textilfarben Gmbh & Co. Deutschland Kg | Orange dye mixtures of fiber-reactive azo dyes and use thereof for dyeing material containing hydroxy-and/or carboxamido groups |
-
1999
- 1999-02-16 US US09/249,756 patent/US6015439A/en not_active Expired - Lifetime
-
2000
- 2000-02-09 CN CN00802863A patent/CN1120864C/zh not_active Expired - Lifetime
- 2000-02-09 AU AU28033/00A patent/AU2803300A/en not_active Abandoned
- 2000-02-09 WO PCT/EP2000/001010 patent/WO2000049093A1/en active IP Right Grant
- 2000-02-09 EP EP00906301A patent/EP1155089B1/en not_active Expired - Lifetime
- 2000-02-09 KR KR1020017010228A patent/KR100607566B1/ko active IP Right Grant
- 2000-02-09 DE DE60001152T patent/DE60001152T2/de not_active Expired - Lifetime
- 2000-02-09 JP JP2000599826A patent/JP4535415B2/ja not_active Expired - Lifetime
- 2000-02-09 TR TR2001/02353T patent/TR200102353T2/xx unknown
Cited By (1)
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WO2005058875A1 (fr) * | 2003-12-19 | 2005-06-30 | Shanghai Institute Of Materia Medica, Chinese Academy Of Sciences | Composes de piperazine triazine, leur obtention, et preparations pharmaceutiques les contenant |
Also Published As
Publication number | Publication date |
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WO2000049093A1 (en) | 2000-08-24 |
TR200102353T2 (tr) | 2002-03-21 |
DE60001152T2 (de) | 2003-11-06 |
KR100607566B1 (ko) | 2006-08-03 |
EP1155089A1 (en) | 2001-11-21 |
KR20020000764A (ko) | 2002-01-05 |
DE60001152D1 (de) | 2003-02-13 |
AU2803300A (en) | 2000-09-04 |
CN1120864C (zh) | 2003-09-10 |
JP2002537436A (ja) | 2002-11-05 |
US6015439A (en) | 2000-01-18 |
EP1155089B1 (en) | 2003-01-08 |
JP4535415B2 (ja) | 2010-09-01 |
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