CN109457512B - Waterless dyeing method for dyeing and fixing deep-tone cotton fabric step by step - Google Patents
Waterless dyeing method for dyeing and fixing deep-tone cotton fabric step by step Download PDFInfo
- Publication number
- CN109457512B CN109457512B CN201811373635.0A CN201811373635A CN109457512B CN 109457512 B CN109457512 B CN 109457512B CN 201811373635 A CN201811373635 A CN 201811373635A CN 109457512 B CN109457512 B CN 109457512B
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- Prior art keywords
- dye
- dyeing
- formula
- anhydrous
- dye compound
- Prior art date
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- 238000004043 dyeing Methods 0.000 title claims abstract description 126
- 239000004744 fabric Substances 0.000 title claims abstract description 82
- 229920000742 Cotton Polymers 0.000 title claims abstract description 77
- 238000000034 method Methods 0.000 title claims abstract description 58
- 239000000975 dye Substances 0.000 claims abstract description 292
- 239000000203 mixture Substances 0.000 claims abstract description 85
- 239000002904 solvent Substances 0.000 claims abstract description 50
- 150000007530 organic bases Chemical class 0.000 claims abstract description 32
- 239000000985 reactive dye Substances 0.000 claims abstract description 17
- 150000001875 compounds Chemical class 0.000 claims description 104
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 73
- XLLIQLLCWZCATF-UHFFFAOYSA-N ethylene glycol monomethyl ether acetate Natural products COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 claims description 70
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 claims description 58
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 40
- 239000002585 base Substances 0.000 claims description 36
- KYVBNYUBXIEUFW-UHFFFAOYSA-N 1,1,3,3-tetramethylguanidine Chemical compound CN(C)C(=N)N(C)C KYVBNYUBXIEUFW-UHFFFAOYSA-N 0.000 claims description 29
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 claims description 29
- 230000008961 swelling Effects 0.000 claims description 26
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 20
- 239000002798 polar solvent Substances 0.000 claims description 18
- 229940126062 Compound A Drugs 0.000 claims description 16
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims description 16
- 229910052700 potassium Inorganic materials 0.000 claims description 15
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- 229910052708 sodium Inorganic materials 0.000 claims description 12
- 239000011734 sodium Substances 0.000 claims description 12
- 238000001035 drying Methods 0.000 claims description 11
- 238000010438 heat treatment Methods 0.000 claims description 11
- 238000001816 cooling Methods 0.000 claims description 10
- 238000004140 cleaning Methods 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 17
- 230000006872 improvement Effects 0.000 abstract description 12
- 239000002351 wastewater Substances 0.000 abstract description 10
- 238000005406 washing Methods 0.000 description 19
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 16
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 16
- 150000007529 inorganic bases Chemical class 0.000 description 14
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
- 230000008569 process Effects 0.000 description 12
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 9
- 239000003960 organic solvent Substances 0.000 description 9
- 239000001488 sodium phosphate Substances 0.000 description 9
- 229910000162 sodium phosphate Inorganic materials 0.000 description 9
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 9
- 238000002156 mixing Methods 0.000 description 8
- 229910000027 potassium carbonate Inorganic materials 0.000 description 8
- 229910000160 potassium phosphate Inorganic materials 0.000 description 8
- 235000011009 potassium phosphates Nutrition 0.000 description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 239000004111 Potassium silicate Substances 0.000 description 6
- 239000004115 Sodium Silicate Substances 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- ZPWVASYFFYYZEW-UHFFFAOYSA-L dipotassium hydrogen phosphate Chemical compound [K+].[K+].OP([O-])([O-])=O ZPWVASYFFYYZEW-UHFFFAOYSA-L 0.000 description 6
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 6
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 description 6
- 229910052913 potassium silicate Inorganic materials 0.000 description 6
- 235000019353 potassium silicate Nutrition 0.000 description 6
- 150000003254 radicals Chemical class 0.000 description 6
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 6
- 229910052911 sodium silicate Inorganic materials 0.000 description 6
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 6
- 238000009210 therapy by ultrasound Methods 0.000 description 6
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 4
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
- 239000003513 alkali Substances 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 239000012530 fluid Substances 0.000 description 4
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 4
- 239000011591 potassium Substances 0.000 description 4
- 235000007686 potassium Nutrition 0.000 description 4
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 4
- 229940048086 sodium pyrophosphate Drugs 0.000 description 4
- 235000019832 sodium triphosphate Nutrition 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- RYCLIXPGLDDLTM-UHFFFAOYSA-J tetrapotassium;phosphonato phosphate Chemical compound [K+].[K+].[K+].[K+].[O-]P([O-])(=O)OP([O-])([O-])=O RYCLIXPGLDDLTM-UHFFFAOYSA-J 0.000 description 4
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- -1 alicyclic hydrocarbon Chemical class 0.000 description 3
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- 239000012442 inert solvent Substances 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 3
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- SYBYTAAJFKOIEJ-UHFFFAOYSA-N 3-Methylbutan-2-one Chemical compound CC(C)C(C)=O SYBYTAAJFKOIEJ-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
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- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- QARVLSVVCXYDNA-UHFFFAOYSA-N bromobenzene Chemical compound BrC1=CC=CC=C1 QARVLSVVCXYDNA-UHFFFAOYSA-N 0.000 description 2
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- 230000007547 defect Effects 0.000 description 2
- AFOSIXZFDONLBT-UHFFFAOYSA-N divinyl sulfone Chemical compound C=CS(=O)(=O)C=C AFOSIXZFDONLBT-UHFFFAOYSA-N 0.000 description 2
- 239000013505 freshwater Substances 0.000 description 2
- 238000005469 granulation Methods 0.000 description 2
- 230000003179 granulation Effects 0.000 description 2
- 150000008282 halocarbons Chemical class 0.000 description 2
- 229940005740 hexametaphosphate Drugs 0.000 description 2
- 239000004312 hexamethylene tetramine Substances 0.000 description 2
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical group CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 2
- 229960004011 methenamine Drugs 0.000 description 2
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 description 2
- 238000005935 nucleophilic addition reaction Methods 0.000 description 2
- 238000010534 nucleophilic substitution reaction Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 235000011118 potassium hydroxide Nutrition 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 2
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- LZDKZFUFMNSQCJ-UHFFFAOYSA-N 1,2-diethoxyethane Chemical compound CCOCCOCC LZDKZFUFMNSQCJ-UHFFFAOYSA-N 0.000 description 1
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- GDXHBFHOEYVPED-UHFFFAOYSA-N 1-(2-butoxyethoxy)butane Chemical compound CCCCOCCOCCCC GDXHBFHOEYVPED-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- 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
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/38—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed 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
- D06P3/60—Natural or regenerated cellulose
- D06P3/66—Natural or regenerated cellulose 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
- D06P5/00—Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
- D06P5/02—After-treatment
- D06P5/04—After-treatment with organic compounds
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- Engineering & Computer Science (AREA)
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Abstract
The invention discloses an anhydrous dyeing method for dyeing and fixing dark-tone cotton fabrics step by step, which comprises the steps of placing the cotton fabrics in an anhydrous dye bath for dyeing; the anhydrous dye bath is obtained by dissolving a reactive dye in an anhydrous solvent, wherein the reactive dye is selected from a reactive black dye composition. The method comprises further adding a fixing base comprising mainly an organic base to the anhydrous dye bath after the target temperature is reached. The waterless dyeing method can solve the problems of wastewater discharge, deep dyeing tone, black degree improvement of black cotton fabrics and the like caused by water bath dyeing, can provide a color fixing rate higher than that of the prior art, and can improve the dyeing fastness of waterless dyeing.
Description
Technical Field
The invention belongs to the technical field of printing and dyeing, relates to an anhydrous dyeing method of cotton fabrics, and particularly relates to an anhydrous dyeing method for dyeing and fixing deep-tone cotton fabrics step by step.
Background
At present, cotton fabric dyeing is mainly carried out by nucleophilic substitution or addition reaction of reactive groups of reactive dyes and hydroxyl groups on fabric fibers to form chemical bonds. This is usually carried out in a water bath. Since water molecules are also good nucleophiles, there are also competing reactions in solution, which are either dye hydrolysis or chemical bond cleavage. In addition, color fixing is usually required after dyeing, and common color fixing agents such as sodium carbonate and sodium phosphate are alkaline substances. This further exacerbates the degree of dye hydrolysis, resulting in poor dye fixation and large amounts of unfixed dye remaining in the bath. When cotton fabrics are dyed in dark shades, especially black, the fixation rate of such dyes is usually only around 60%, and the amount of wasted dyes is as high as more than one third.
Furthermore, the greatest problem of bath staining is the increasing ecological risk caused by the wastewater. In addition to the presence of large amounts of dyes, the dye-accelerating electrolytes and fixing bases, as well as other common dyes, are included in the dye bath, resulting in high wastewater chromaticity, high salinity, high chemical oxygen demand, and high wastewater treatment difficulty. Furthermore, the washing step after the fixation step requires a large amount of fresh water, and statistically, 50-110kg of fresh water is consumed on average per 1kg of cotton fabric. The clean water is also converted into printing and dyeing wastewater.
In order to solve the problem of waste water discharge of cotton fabric dyeing from the source, in recent years, people gradually shift the sight to an anhydrous dyeing method. Common anhydrous dyeing methods include supercritical fluid dyeing, reverse micelle dyeing, vacuum sublimation dyeing, suspension dyeing, organic solvent dyeing, and the like. The above methods have in common the use of other solvents or fluid systems to replace water or to reduce the amount of water used in the dyeing process. Among these, of more interest are supercritical fluid dyeing and organic solvent dyeing, both of which almost completely avoid the involvement of water.
However, both supercritical fluid dyeing and organic solvent dyeing have the defects of few kinds of applicable dyes, poor compatibility of a dyeing system, difficulty in deep color dyeing and the like. This drawback is particularly evident when the cotton fabric is dyed to dark shades, in particular black, with the result that the apparent depth of colour (i.e. blackness) is difficult to increase. If the defects can not be solved, the market popularization is difficult to complete. Because nearly half of the dyes currently on the market are used for dyeing cotton fabrics black. The idea of water bath dyeing can be used for reference, namely, the reactive dye composition is adopted to dye dark tone or improve blackness, however, as the anhydrous solvent system is completely different from water, the solubility, compatibility and other properties of the dye in different systems are greatly different, and the water bath dyeing original class is difficult to transplant. Furthermore, organic solvent dyeing also requires fixing and fastness of dyeing problems. According to the literature research situation, no literature report that the reactive dye composition is used in a non-aqueous solvent system to solve the dark color and provide better color fastness is found.
Therefore, there is an urgent need for continued improvement over existing anhydrous dyeing methods.
Disclosure of Invention
In view of the above-mentioned drawbacks of the prior art, the present invention is directed to solving at least one or more of the problems of wastewater discharge, deep dyeing tone, blackness improvement of black cotton fabric, color fixation of a coordinated reactive dye composition, and improvement of the color fastness of waterless dyeing, especially the most common color fastness to rubbing and color fastness to washing.
Further, the invention aims to simultaneously solve the problems of waste water discharge, deep color dyeing, black degree improvement of black cotton fabrics and the like caused by water bath dyeing.
Furthermore, the invention aims to simultaneously solve the problems of waste water discharge, deep color dyeing, black degree improvement of black cotton fabrics, color fixation rate equivalent to that of the prior art and the like caused by water bath dyeing.
Still further, the invention aims to simultaneously solve the problems of waste water discharge, deep color dyeing, black degree improvement of black cotton fabrics, color fixation rate higher than that of the prior art and the like caused by water bath dyeing.
And, still further, the present invention is directed to simultaneously solve the problems of wastewater discharge, deep dyeing tone, improvement of blackness of black cotton fabric, coordination of fixation ratio of reactive dye composition, improvement of dyeing fastness of waterless dyeing, etc. caused by water bath dyeing.
In order to solve the problems, the invention adopts the following technical scheme: a waterless dyeing method for dyeing and fixing dark-tone cotton fabric step by step comprises the following steps: placing the cotton fabric in an anhydrous dye bath, heating at a certain speed, keeping the temperature after reaching a target temperature, and dyeing for a certain time; cooling to room temperature after dyeing is finished, cleaning the dyed fabric by using an anhydrous solvent, and finally drying to obtain a dyed cotton fabric; wherein the anhydrous dye bath is obtained by dissolving a reactive dye in an anhydrous solvent, and the reactive dye is selected from a reactive black dye composition; characterized in that the process comprises the further addition of a fixing base comprising mainly an organic base in the anhydrous dye bath after the target temperature has been reached.
According to the anhydrous dyeing method, the reactive black dye composition consists of a dye compound A, a dye compound B and a dye compound C; wherein,
the dye compound A is selected from any one or more of dye compounds shown in a formula (I);
in the formula (I), R1-R4Each independently selected from H, C1-C4Alkyl radical, C1-C4Alkoxy and SO3M;Y1-Y2Each independently selected from SO2CH=CH2Or SO2CH2CH2OSO3M; m is selected from H, Na orK;
The dye compound B is selected from any one or more of dye compounds shown in a formula (II);
in the formula (II), R5-R8Each independently selected from H, C1-C4Alkyl radical, C1-C4Alkoxy and SO3M;Y3-Y4Each independently selected from SO2CH=CH2Or SO2CH2CH2OSO3M; m is selected from H, Na or K;
the dye compound C is selected from any one or more of dye compounds shown in a formula (III);
in the formula (III), R9-R10Each independently selected from H, C1-C4Alkyl radical, C1-C4Alkoxy and SO3M;Y5Independently selected from SO2CH=CH2Or SO2CH2CH2OSO3M; m is selected from H, Na or K.
The anhydrous dyeing method according to the invention, wherein the dye compound A is selected from the dye compounds represented by the formula (I-1) or (I-2),
the anhydrous dyeing method according to the invention, wherein the dye compound B is selected from the dye compounds represented by the formula (II-1) or (II-2),
the anhydrous dyeing method according to the invention, wherein the dye compound C is selected from the dye compounds represented by the formula (III-1) or (III-2),
the anhydrous dyeing method is characterized in that the weight percentage of the dye compound A is 45-85 percent based on the total weight of the reactive black dye composition; the weight percentage of the dye compound B is 15-35%; the weight percentage of the dye compound C is 5-18%.
The anhydrous dyeing method is characterized in that the weight percentage of the dye compound A is 60-70 percent based on the total weight of the reactive black dye composition; the weight percentage of the dye compound B is 22-28%; the weight percentage of the dye compound C is 8-12%.
The anhydrous dyeing method according to the invention, wherein the fixing base is selected from a mixture of triethylene diamine, tetramethyl guanidine and sodium carbonate.
According to the anhydrous dyeing method, the weight ratio of the triethylene diamine to the tetramethyl guanidine to the sodium carbonate is (1.5-2): 1: (0.01-0.3).
According to the anhydrous dyeing method, the cotton fabric is swelled by dimethyl sulfoxide in advance.
Reactive dyes
The reactive dye of the present invention is selected from reactive black dye compositions.
Further, the reactive black dye composition comprises a dye compound A, wherein the dye compound A is selected from any one or more of dye compounds shown in a formula (I);
in the formula (I), R1-R4Each independently selected from H, C1-C4Alkyl radical, C1-C4Alkoxy and SO3M;Y1-Y2Each independently selected from SO2CH=CH2Or SO2CH2CH2OSO3M; m is selected from H, Na or K.
Further, the reactive black dye composition also comprises a dye compound B and a dye compound C; wherein,
the dye compound B is selected from any one or more of dye compounds shown in a formula (II);
in the formula (II), R5-R8Each independently selected from H, C1-C4Alkyl radical, C1-C4Alkoxy and SO3M;Y3-Y4Each independently selected from SO2CH=CH2Or SO2CH2CH2OSO3M; m is selected from H, Na or K;
the dye compound C is selected from any one or more of dye compounds shown in a formula (III);
in the formula (III), R9-R10Each independently selected from H, C1-C4Alkyl radical, C1-C4Alkoxy and SO3M;Y5Independently selected from SO2CH=CH2Or SO2CH2CH2OSO3M; m is selected from H, Na or K.
In a preferred embodiment, the dye compound a is selected from any one or more of the dye compounds represented by formula (I');
in the formula (I'), Y1-Y2Each independently selected from SO2CH=CH2Or SO2CH2CH2OSO3M; m is selected from H, Na or K;
the dye compound B is selected from any one or more of dye compounds shown in a formula (II');
in the formula (II'), R6Selected from SO3M;R7-R8Each independently selected from C1-C4Alkyl and C1-C4An alkoxy group; y is3-Y4Each independently selected from SO2CH=CH2Or SO2CH2CH2OSO3M; m is selected from H, Na or K;
the dye compound C is selected from any one or more of dye compounds shown in a formula (III');
in the formula (III), Y5Independently selected from SO2CH=CH2Or SO2CH2CH2OSO3M; m is selected from H, Na or K.
In a specific embodiment, the dye compound A is selected from the dye compounds represented by the formula (I-1),
in another embodiment, the dye compound A is selected from the dye compounds represented by the formula (I-2),
in a specific embodiment, the dye compound B is selected from the dye compounds represented by the formula (II-1),
in another embodiment, the dye compound B is selected from the dye compounds represented by the formula (II-2),
in a specific embodiment, the dye compound C is selected from the dye compounds represented by the formula (III-1),
in another embodiment, the dye compound C is selected from the dye compounds represented by the formula (III-2),
in the present invention, the dye compound is derived from a commercially known product, and can be prepared according to a known method.
Most preferably, the dye compound A, the dye compound B and the dye compound C of the present invention are selected from the dye compounds represented by the formula (I-1), the dye compounds represented by the formula (II-1) and the dye compounds represented by the formula (III-1).
Of course, those skilled in the art know that the dye compounds represented by the formula (I-2), the dye compounds represented by the formula (II-2), and the dye compounds represented by the formula (III-2) may be used instead of the above dye compounds because they can be converted into the dye compounds represented by the formula (I-1), the dye compounds represented by the formula (II-1), and the dye compounds represented by the formula (III-1) under basic conditions.
Advantageously, when the dye compound represented by the formula (I-2), the dye compound represented by the formula (II-2) or the dye compound represented by the formula (III-2) is used, a base is added to form a vinylsulfone dye compound before use, and then the mixture is precipitated under neutral conditions. And extracting the crude product by using an organic solvent, and distilling under reduced pressure to obtain the high-purity vinyl sulfone dye compound.
Further, as the reactive black dye composition of the present invention, a dye compound a, a dye compound B and a dye compound C are mainly included.
In the above embodiments, "mainly comprising" generally means that other dye components are optionally included in addition to the dye compound a, the dye compound B, and the dye compound C; however, the dye compound A, the dye compound B and the dye compound C account for more than 70%, preferably more than 80%, more preferably more than 90%, and most preferably more than 95% of the total weight of all the dye components.
In a preferred embodiment, "consisting essentially of means that the ratio of the total weight of the dye compound a, the dye compound B and the dye compound C to the weight of the reactive black dye composition is not less than 90%; preferably not less than 95%; more preferably not less than 97%; and, most preferably not less than 98%.
In a further preferred embodiment, the reactive black dye composition according to the invention consists of a dye compound a, a dye compound B and a dye compound C. That is, the reactive black dye composition of the present invention is obtained by mixing the dye compound a, the dye compound B and the dye compound C.
Advantageously, the mixing can be either dry or wet.
In the dry mixing embodiment, the dye compounds are dry mixed using dye granules obtained by extrusion granulation or spray drying granulation. Advantageously, the particle size of the dye particles is 100-2000 μm, preferably 150-1500 μm, more preferably 200-1000 μm, and most preferably 200-500 μm.
In the wet mixing embodiment, the dye compounds are slurried in a ratio, agitated in a kettle, blended, and then spray dried.
The weight percentage of the dye compound a is 45-85% based on the total weight of the reactive black dye composition.
Preferably, the dye compound a is present in an amount of 50 to 80% by weight, based on the total weight of the reactive black dye composition.
More preferably, the weight percentage of the dye compound a is 55-75% based on the total weight of the reactive black dye composition.
And, most preferably, the weight percentage of the dye compound a is 60 to 70% based on the total weight of the reactive black dye composition.
In a specific embodiment, the weight percentage of dye compound a is 65% based on the total weight of the reactive black dye composition.
The weight percentage of the dye compound B is 15-35% based on the total weight of the reactive black dye composition.
Preferably, the weight percentage of the dye compound B is 18-32% based on the total weight of the reactive black dye composition.
More preferably, the weight percentage of the dye compound B is 20-30% based on the total weight of the reactive black dye composition.
And, most preferably, the weight percentage of the dye compound B is 22-28% based on the total weight of the reactive black dye composition.
In a specific embodiment, the dye compound B is present in an amount of 25% by weight, based on the total weight of the reactive black dye composition.
The dye compound C is present in an amount of 5 to 18% by weight, based on the total weight of the reactive black dye composition.
Preferably, the dye compound C is present in an amount of 6 to 16% by weight, based on the total weight of the reactive black dye composition.
More preferably, the weight percentage of the dye compound C is 7-14% based on the total weight of the reactive black dye composition.
And, most preferably, the weight percentage of the dye compound C is 8-12% based on the total weight of the reactive black dye composition.
In a specific embodiment, the dye compound C is present in an amount of 10% by weight, based on the total weight of the reactive black dye composition.
Anhydrous solvent
The anhydrous solvent of the invention mainly comprises ethylene glycol monomethyl ether acetate and an aprotic polar solvent.
In the present invention, "mainly consisting of …" means that the anhydrous solvent optionally includes other organic solvents in addition to ethylene glycol monomethyl ether acetate and the aprotic polar solvent, but the sum of the volumes of ethylene glycol monomethyl ether acetate and the aprotic polar solvent accounts for 90% or more, preferably 95% or more, more preferably 97% or more, and most preferably 98% or more of the sum of the volumes of all the solvents. In one embodiment, the volume of ethylene glycol monomethyl ether acetate is 65 units, the volume of the aprotic polar solvent is 30 units, and the volume of the other organic solvent is 5 units.
Advantageously, the volume ratio of ethylene glycol monomethyl ether acetate to aprotic polar solvent is (55-80): (45-20). Preferably, the volume ratio of the ethylene glycol monomethyl ether acetate to the aprotic polar solvent is (60-80): (40-20); more preferably, the volume ratio of ethylene glycol monomethyl ether acetate to aprotic polar solvent is (65-80): (35-20); and, most preferably, the volume ratio of ethylene glycol monomethyl ether acetate to aprotic polar solvent is (65-75): (35-25).
In a specific embodiment, the volume ratio of ethylene glycol monomethyl ether acetate to aprotic polar solvent is 70: 30.
in a preferred embodiment, the anhydrous solvent of the present invention consists of ethylene glycol monomethyl ether acetate and an aprotic polar solvent.
As the aprotic polar solvent of the present invention, dimethyl sulfoxide, dimethylformamide, dimethylacetamide, sulfolane, acetonitrile, acetone and hexamethylphosphoramide are included.
Preferably, the aprotic polar solvent is selected from a mixture of any one or more of dimethyl sulfoxide, dimethylformamide, dimethylacetamide, sulfolane, acetonitrile and acetone.
More preferably, the aprotic polar solvent is selected from a mixture of any one or more of dimethyl sulfoxide, dimethylformamide, dimethylacetamide, sulfolane and acetonitrile.
And, most preferably, the aprotic polar solvent is selected from a mixture of any one or more of dimethyl sulfoxide, dimethylformamide and dimethylacetamide.
In a particular embodiment, the aprotic polar solvent is selected from dimethyl sulfoxide.
As other organic solvents of the present invention, there may be mentioned, but not limited to, aromatic hydrocarbon solvents, aliphatic hydrocarbon solvents, alicyclic hydrocarbon solvents, halogenated hydrocarbon solvents, alcohol solvents, ether solvents, ester solvents, ketone solvents, polyol solvents and the like.
As the aromatic hydrocarbon solvent, for example, benzene, toluene, ethylbenzene, o-xylene, m-xylene and p-xylene, and the like can be cited.
As the aliphatic hydrocarbon solvent, for example, pentane, hexane, octane and petroleum ether having a boiling point of 60 to 90 ℃ and the like can be mentioned.
Examples of the alicyclic hydrocarbon solvent include cyclopentane, cyclohexane, cyclohexanone, tolucyclohexanone, and the like.
Examples of the halogenated hydrocarbon solvent include chlorobenzene, o-dichlorobenzene, m-dichlorobenzene, p-dichlorobenzene, bromobenzene, dichloromethane, and trichloromethane.
Examples of the alcohol solvent include methanol, ethanol, propanol, isopropanol, butanol, and isobutanol.
Examples of the ether solvent include methyl ether, ethyl ether, methylethyl ether, propylene oxide, tetrahydrofuran, dioxane, and the like.
Examples of the ester solvent include methyl formate, ethyl formate, methyl acetate, ethyl acetate, propyl acetate, and the like.
Examples of the ketone solvent include acetone, methyl ethyl ketone, methyl isopropyl ketone, methyl n-butanone, methyl isobutyl ketone, and the like.
Examples of the polyhydric alcohol solvent include ethylene glycol, glycerol, ethylene glycol, monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monopropyl ether, ethylene glycol monobutyl ether, ethylene glycol dimethyl ether, ethylene glycol diethyl ether, ethylene glycol dipropyl ether, and ethylene glycol dibutyl ether.
As the remaining solvent, for example, dimethyl carbonate, phenol, and the like can be mentioned.
In view of the anhydrous solvent system and the dyeing and fixing mechanism of the present invention, as other organic solvents, it is preferable that the dyeing and fixing reaction is not disturbed. Such solvents may be considered inert solvents. In a particular embodiment, the inert solvent may be acetone. In another specific embodiment, the inert solvent may be dioxane.
However, as a most preferred embodiment, the anhydrous solvent of the present invention consists of ethylene glycol monomethyl ether acetate and dimethyl sulfoxide. That is, the anhydrous solvent of the present invention is a mixture of ethylene glycol monomethyl ether acetate and dimethyl sulfoxide.
Without wishing to be bound by any theory, the anhydrous solvent system of the present invention eliminates hydrolysis of the disperse black dye composition, and to some extent, improves dye uptake and fixation.
Advantageously, the volume ratio of ethylene glycol monomethyl ether acetate to dimethyl sulfoxide is (55-80): (45-20). Preferably, the volume ratio of the ethylene glycol monomethyl ether acetate to the dimethyl sulfoxide is (60-80): (40-20); more preferably, the volume ratio of ethylene glycol monomethyl ether acetate to dimethyl sulfoxide is (65-80): (35-20); and, most preferably, the volume ratio of ethylene glycol monomethyl ether acetate to dimethyl sulfoxide is (65-75): (35-25).
In a specific embodiment, the volume ratio of ethylene glycol monomethyl ether acetate to dimethyl sulfoxide is 70: 30.
the anhydrous solvent system with the specific composition further improves the dyeing fixation rate of the invention.
Color fixing base
In the process of the present invention, it is preferred to add a fixing base in view of fixing and improving dyeing properties.
The fixing base of the present invention may be theoretically an inorganic base or an organic base.
As the inorganic base, sodium carbonate, sodium phosphate, potassium carbonate, potassium phosphate, sodium silicate, potassium silicate, disodium hydrogen phosphate, dipotassium hydrogen phosphate, sodium pyrophosphate, potassium pyrophosphate, sodium hydroxide, potassium hydroxide, sodium tripolyphosphate, potassium tripolyphosphate, sodium hexametaphosphate, and potassium hexametaphosphate, and mixtures thereof can be mentioned.
Preferably, the inorganic base is selected from the group consisting of sodium carbonate, sodium phosphate, potassium carbonate, potassium phosphate, sodium silicate, potassium silicate, disodium hydrogen phosphate, dipotassium hydrogen phosphate, sodium pyrophosphate, potassium pyrophosphate, and mixtures thereof.
More preferably, the inorganic base is selected from the group consisting of sodium carbonate, sodium phosphate, potassium carbonate, potassium phosphate, sodium silicate, potassium silicate, disodium hydrogen phosphate, dipotassium hydrogen phosphate, and mixtures thereof.
And, most preferably, the inorganic base is selected from the group consisting of sodium carbonate, sodium phosphate, potassium carbonate, potassium phosphate, and mixtures thereof.
The addition of the inorganic base can improve the dyeing fixation rate, but the solubility of the inorganic base in the anhydrous solvent system is limited; in addition, the inorganic bases have a limited degree of improvement in the dye fixation of the present invention at the same concentration. Thus, as the fixing base of the present invention, preference is given to organic bases; or primarily an organic base.
In one embodiment, as the fixing base of the present invention, an organic base is preferred.
As the organic base of the present invention, triethylene diamine, tetramethyl guanidine, hexamethylene tetramine, and mixtures thereof are selected.
In the invention, the addition of the organic alkali can obviously improve the dyeing fixation rate of the invention. In the case of not using organic alkali, although cotton fabrics with high degree of blackness can be obtained only depending on the used reactive dye and anhydrous solvent, the dyeing fixation rate is low and is only about 10%. This results in inefficient dyeing and significant waste of dye. Under the condition of using organic alkali, if only triethylene diamine is used, the dyeing fixation rate can reach about 65 percent at most; if only tetramethyl guanidine is used, the dyeing fixation rate can reach about 60 percent at most; whereas, if only hexamethylenetetramine is used, the dye fixation is generally around 30-40%.
Therefore, preferably, as the organic base of the present invention, triethylenediamine, tetramethylguanidine, and a mixture thereof are selected. When these organic bases are used, the dye fixation of the present invention is at least comparable to, or significantly higher than, existing aqueous dyeing processes.
In order to further improve the dyeing efficiency, the composition of an anhydrous solvent system needs to be optimized, and the mixture of triethylene diamine and tetramethyl guanidine is used as a color fixing base, so that the dyeing color fixing rate can be obviously improved. The inventor finds that the dye fixation rate of the invention can be optimized to 70-80% under the same other process parameters by adjusting the weight ratio of triethylene diamine and tetramethyl guanidine within a specific value range.
Advantageously, in the mixture of triethylenediamine and tetramethylguanidine, the weight ratio of triethylenediamine to tetramethylguanidine is (1.5-2): 1, preferably (1.5-1.9): 1, more preferably (1.5-1.8): 1, and, most preferably, (1.5-1.7): 1.
in a specific embodiment, the fixing base is selected from a mixture of triethylene diamine and tetramethyl guanidine, wherein the weight ratio of triethylene diamine to tetramethyl guanidine is 1.6: 1.
without wishing to be bound by any theory, since dyeing is carried out in an anhydrous solvent, the organic base of the specific composition of the present invention interacts with the dye compound a, the dye compound B and the dye compound C of the present invention, respectively, and finally promotes the nucleophilic addition or nucleophilic substitution reaction of the disperse black dye composition with the hydroxyl group on the cotton fiber. In contrast, triethylene diamine is more beneficial to improving the fixation rate of the dye compound A; and the tetramethylguanidine is more beneficial to improving the fixation rate of the dye compound B and the dye compound C.
On the other hand, for the effect on the fastness of dyeing, the organic bases of the specific composition according to the invention likewise have a greater effect on smooth cotton fabric fibers and on enhancing the dye-fiber interaction. The test result shows that the color fastness to rubbing and washing is improved.
In another embodiment, the fixing base of the present invention comprises primarily an organic base.
In the above embodiments, "consisting essentially of means that the fixation base optionally includes other organic and inorganic bases in addition to the organic base; but the weight of organic base is more than 90%, preferably more than 95%, more preferably more than 97%, and most preferably more than 98% of the sum of the weight of all fixing bases. Preferably, the fixing base optionally comprises an inorganic base as described above in addition to the organic base.
As the inorganic base, sodium carbonate, sodium phosphate, potassium carbonate, potassium phosphate, sodium silicate, potassium silicate, disodium hydrogen phosphate, dipotassium hydrogen phosphate, sodium pyrophosphate, potassium pyrophosphate, sodium hydroxide, potassium hydroxide, sodium tripolyphosphate, potassium tripolyphosphate, sodium hexametaphosphate, and potassium hexametaphosphate, and mixtures thereof can be mentioned.
Preferably, the inorganic base is selected from the group consisting of sodium carbonate, sodium phosphate, potassium carbonate, potassium phosphate, sodium silicate, potassium silicate, disodium hydrogen phosphate, dipotassium hydrogen phosphate, sodium pyrophosphate, potassium pyrophosphate, and mixtures thereof.
More preferably, the inorganic base is selected from the group consisting of sodium carbonate, sodium phosphate, potassium carbonate, potassium phosphate, sodium silicate, potassium silicate, disodium hydrogen phosphate, dipotassium hydrogen phosphate, and mixtures thereof.
And, most preferably, the inorganic base is selected from the group consisting of sodium carbonate, sodium phosphate, potassium carbonate, potassium phosphate, and mixtures thereof.
In a particular embodiment, the fixing base is selected from a mixture of triethylenediamine, tetramethylguanidine and sodium carbonate.
Advantageously, in the mixture of triethylenediamine, tetramethylguanidine and sodium carbonate, the weight ratio of triethylenediamine, tetramethylguanidine and sodium carbonate is (1.5-2): 1: (0.01-0.3), preferably (1.5-1.9): 1: (0.01-0.25), more preferably (1.5-1.8): 1: (0.01-0.2), and, most preferably, (1.5-1.7): 1: (0.01-0.15).
In a more specific embodiment, the fixing base is selected from a mixture of triethylene diamine, tetramethyl guanidine and sodium carbonate in a weight ratio of 1.5: 1: 0.1.
dyeing method
The dyeing method of the invention comprises the steps of placing the cotton fabric in an anhydrous dye bath, heating at a certain speed, keeping the temperature after reaching the target temperature, and dyeing for a certain time; and cooling to room temperature after dyeing is finished, washing the dyed fabric by using an anhydrous solvent, and finally drying to obtain the dyed cotton fabric.
The anhydrous dye bath is obtained by dissolving the reactive dye (or the reactive black dye composition) in the anhydrous solvent.
In the present invention, the bath ratio of the cotton fabric (dry weight) to the anhydrous dye bath is 1: (8-25) g/mL.
Preferably, the bath ratio of the cotton fabric to the anhydrous dye bath is 1: (10-22) g/mL; more preferably, the bath ratio of the cotton fabric to the anhydrous dye bath is 1: (12-20) g/mL; and, most preferably, the bath ratio of the cotton fabric to the anhydrous dye bath is 1: (14-18) g/mL.
In a specific embodiment, the bath ratio of the cotton fabric to the anhydrous dye bath is 1: 16 g/mL.
In the present invention, the amount of the dye is 2 to 6 o.w.f..
Specifically, the dye amount is 2 o.w.f%, 3 o.w.f%, 4 o.w.f%, 5 o.w.f%, 6 o.w.f%.
Preferably, the dye is used in an amount of 2-5 o.w.f%; more preferably, the dye is used in an amount of 3-5 o.w.f..
In one embodiment, the dye is present in an amount of 4 o.w.f..
In the invention, the heating rate of dyeing is 0.5-5 ℃/min.
Preferably, the heating rate is 1-4.5 ℃/min; more preferably, the temperature rise rate is 1.5-4 ℃/min; and, most preferably, the rate of temperature rise is 2-3.5 ℃/min.
In a specific embodiment, the temperature ramp rate is 3 ℃/min.
In the present invention, the target temperature for dyeing is 70 to 100 ℃.
Preferably, the target temperature is 75-95 ℃; more preferably, the target temperature is 80-95 ℃; and, most preferably, the target temperature is 80-90 ℃.
In a specific embodiment, the target temperature is 85 ℃.
In the present invention, the dyeing time is 1 to 12 hours.
Preferably, the dyeing time is 2-10 h; more preferably, the dyeing time is 3-8 h; and, most preferably, the dyeing time is 4-6 h.
In a specific embodiment, the staining time is 5 h.
In the invention, the method further comprises the step of adding a fixing alkali for fixing.
As the fixing base of the present invention, organic bases are preferred; or primarily an organic base.
After cooling to room temperature at the end of dyeing, the washing is advantageously carried out more than once, preferably more than twice, each with ethylene glycol monomethyl ether acetate and with aprotic polar solvents, respectively, until the last wash is colorless.
In a specific embodiment, after the dyeing is finished and cooled to room temperature, the washing is respectively carried out more than once, preferably more than twice by using ethylene glycol monomethyl ether acetate and dimethyl sulfoxide until the washing liquid at the last time is colorless.
More advantageously, the washing is carried out alternately with hot ethylene glycol monomethyl ether acetate and hot dimethyl sulfoxide more than once, preferably more than twice, each until the last washing is colorless.
In the above, "hot" means a temperature between 40 and 60 c, preferably between 45 and 55 c.
In a specific embodiment, "hot" means 50 ℃.
Advantageously, the cotton fabric used as the above-mentioned method is previously subjected to dimethyl sulfoxide swelling. Preferably, the swelling degree of the cotton fabric is between 10 and 30%, more preferably between 15 and 30%, and, most preferably between 20 and 30%.
In a particular embodiment, the cotton fabric has a swelling degree of 22%.
The swelling of the cotton fabric is preferably obtained by soaking at 60-90 deg.C, preferably 70-90 deg.C for 0.5-12h, preferably 1-6 h.
On swelling, the bath ratio is advantageously 1: (10-50); preferably, the bath ratio is advantageously 1: (15-45); more preferably, the bath ratio is advantageously 1: (20-40); and, most preferably, the bath ratio is advantageously 1: (25-35).
In a specific embodiment, the swelling of the cotton fabric is obtained by soaking for 4h at 80 ℃ with a bath ratio of 1: 30. the swelling degree of the product is 22% according to a centrifugal weighing method.
In a preferred embodiment, when a fixing base is used and when the fixing base is the aforementioned organic base, the invention also provides a dyeing process for simultaneous fixing of cotton fabric on dyeing, said process comprising the further addition of the aforementioned organic base to the aforementioned anhydrous dye bath before the start of the temperature increase.
In the present invention, the organic base is added in an amount of 2 to 8 g/L. Preferably, the addition amount of the organic base is 3-8 g/L; more preferably, the addition amount of the organic base is 4-8 g/L; and, most preferably, the organic base is added in an amount of 5 to 8 g/L.
In a specific embodiment, the organic base is added in an amount of 6 g/L.
Advantageously, the cotton fabric used as the above-mentioned method is previously subjected to dimethyl sulfoxide swelling. Preferably, the swelling degree of the cotton fabric is between 10 and 30%, more preferably between 15 and 30%, and, most preferably between 20 and 30%.
In a particular embodiment, the cotton fabric has a swelling degree of 22%.
Swelling of the cotton fabric was carried out as described above.
In another preferred embodiment, when a fixing base is used and when the fixing base mainly comprises the aforementioned organic base, the present invention also provides a dyeing process for fixing cotton fabrics by dyeing in steps, which comprises further adding the aforementioned fixing base in the aforementioned anhydrous dye bath after reaching the target temperature.
In the present invention, the fixing base is added in an amount of 2-8 g/L. Preferably, the addition amount of the fixing base is 3-8 g/L; more preferably, the fixing base is added in an amount of 4-8 g/L; and, most preferably, the fixing base is added in an amount of 5 to 8 g/L.
In a specific embodiment, the fixing base is added in an amount of 6 g/L.
Advantageously, the cotton fabric used as the above-mentioned method is previously subjected to dimethyl sulfoxide swelling. Preferably, the swelling degree of the cotton fabric is between 10 and 30%, more preferably between 15 and 30%, and, most preferably between 20 and 30%.
In a particular embodiment, the cotton fabric has a swelling degree of 22%.
Swelling of the cotton fabric was carried out as described above.
Without wishing to be bound by any theory, swelling contributes to an improved interaction between the cotton fabric fibers and the reactive dyes, thereby increasing the dye fixation of the present invention, while also contributing to further improvement of the fastness to washing.
Detailed Description
The invention will be further illustrated with reference to specific embodiments.
It should be understood that the detailed description of the invention is merely illustrative of the spirit and principles of the invention and is not intended to limit the scope of the invention. Furthermore, it should be understood that various changes, substitutions, deletions, modifications or adjustments may be made by those skilled in the art after reading the disclosure of the present invention, and such equivalents are also within the scope of the invention as defined in the appended claims.
In the present invention, the swelling degree of the cotton fabric is carried out by a centrifugal weighing method. The specific method comprises the following steps: and (3) centrifuging the swelled cotton fabric, drying to constant weight, and measuring the increase percentage of the weight of the cotton fabric relative to the dry weight of the cotton fabric before the swelling process, namely the swelling degree.
The measurement of the apparent color depth Integ value is carried out on a Datacolor color measuring and matching instrument, the dyed fabric is laminated into 4 layers, one point is taken on the front surface and the back surface of each layer, 8 points are measured and the average value is taken.
The fixation rate comprises two fixation rates of each dye component and an absolute fixation rate. The former method is to calculate the concentration of dye before and after fixation by measuring the molar absorption coefficient at the maximum absorption wavelength of each dye component and the absorbance before and after fixation and using the maximum absorption wavelength-simultaneous equation method. The color fixing rate of each dye component is weighted according to the weight proportion of the dye components, and then the color fixing rate is calculated. In the present invention, the fixation ratios are the latter when the case of the specific dye components is not specified.
The crocking fastness and the washing fastness (60 ℃) are determined according to the relevant international standards ISO105-X12 and ISO105-C10, respectively.
Example 1
A reactive black dye composition was prepared by mixing 65% of the dye compound represented by the formula (I-1), 25% of the dye compound represented by the formula (II-1) and 10% of the dye compound represented by the formula (III-1). Dissolving a reactive black dye composition in a solvent with a volume ratio of 70: and (3) obtaining a dye bath from 30 parts of ethylene glycol monomethyl ether acetate and dimethyl sulfoxide in an anhydrous solvent. Then adding a mixture of triethylene diamine and tetramethyl guanidine into an anhydrous dye bath, wherein the weight ratio of the triethylene diamine to the tetramethyl guanidine is 1.6: 1; the amount of organic base added was 6 g/L. And (4) carrying out ultrasonic treatment to obtain a uniform anhydrous dye bath. Placing the cotton fabric which is swelled by dimethyl sulfoxide in advance and has swelling degree of 22% into an anhydrous dye bath. The bath ratio of the cotton fabric to the anhydrous dye bath is 1: 16 g/mL. The dye amount was 4 o.w.f%. Heating at the speed of 3 ℃/min, keeping the temperature after the target temperature is reached to 85 ℃, and dyeing for 5 hours; and after dyeing is finished, cooling to room temperature, alternately washing 3 times by using ethylene glycol monomethyl ether acetate at 50 ℃ and dimethyl sulfoxide at 50 ℃, wherein the dosage of each time is 20mL, and finally drying to obtain the dyed cotton fabric.
Example 2
70% of dye compound shown in formula (I-1), 22% of dye compound shown in formula (II-1) and 8% of dye compound shown in formula (III-1) are mixed to form the reactive black dye composition. Dissolving a reactive black dye composition in a volume ratio of 65: 35 and (3) obtaining a dye bath in an anhydrous solvent of ethylene glycol monomethyl ether acetate and dimethyl sulfoxide. Then adding a mixture of triethylene diamine and tetramethyl guanidine into an anhydrous dye bath, wherein the weight ratio of the triethylene diamine to the tetramethyl guanidine is 1.8: 1; the amount of the organic base added was 8 g/L. And (4) carrying out ultrasonic treatment to obtain a uniform anhydrous dye bath. Placing the cotton fabric which is swelled by dimethyl sulfoxide in advance and has swelling degree of 22% into an anhydrous dye bath. The bath ratio of the cotton fabric to the anhydrous dye bath is 1: 18 g/mL. The dye amount was 4 o.w.f%. Heating at the speed of 3 ℃/min, keeping the temperature after the target temperature is reached to 90 ℃, and dyeing for 4 h; and after dyeing is finished, cooling to room temperature, alternately washing 3 times by using ethylene glycol monomethyl ether acetate at 50 ℃ and dimethyl sulfoxide at 50 ℃, wherein the dosage of each time is 20mL, and finally drying to obtain the dyed cotton fabric.
Example 3
The reactive black dye composition is prepared by mixing 60% of the dye compound shown in the formula (I-1), 28% of the dye compound shown in the formula (II-1) and 12% of the dye compound shown in the formula (III-1). Dissolving a reactive black dye composition in a volume ratio of 75: 25 and the ethylene glycol monomethyl ether acetate and the dimethyl sulfoxide to obtain the dye bath. Then adding a mixture of triethylene diamine and tetramethyl guanidine into an anhydrous dye bath, wherein the weight ratio of the triethylene diamine to the tetramethyl guanidine is 1.5: 1; the amount of the organic base added was 5 g/L. And (4) carrying out ultrasonic treatment to obtain a uniform anhydrous dye bath. Placing the cotton fabric which is swelled by dimethyl sulfoxide in advance and has swelling degree of 22% into an anhydrous dye bath. The bath ratio of the cotton fabric to the anhydrous dye bath is 1: 14 g/mL. The dye amount was 4 o.w.f%. Heating at the speed of 3 ℃/min, keeping the temperature after reaching the target temperature of 80 ℃, and dyeing for 6 hours; and after dyeing is finished, cooling to room temperature, alternately washing 3 times by using ethylene glycol monomethyl ether acetate at 50 ℃ and dimethyl sulfoxide at 50 ℃, wherein the dosage of each time is 20mL, and finally drying to obtain the dyed cotton fabric.
Example 4
A reactive black dye composition was prepared by mixing 65% of the dye compound represented by the formula (I-1), 25% of the dye compound represented by the formula (II-1) and 10% of the dye compound represented by the formula (III-1). Dissolving a reactive black dye composition in a solvent with a volume ratio of 70: and (3) obtaining a dye bath from 30 parts of ethylene glycol monomethyl ether acetate and dimethyl sulfoxide in an anhydrous solvent. And (4) carrying out ultrasonic treatment to obtain a uniform anhydrous dye bath. Placing the cotton fabric which is swelled by dimethyl sulfoxide in advance and has swelling degree of 22% into an anhydrous dye bath. The bath ratio of the cotton fabric to the anhydrous dye bath is 1: 16 g/mL. The dye amount was 4 o.w.f%. Heating at the speed of 3 ℃/min, keeping the temperature after the target temperature is reached to 85 ℃, adding a mixture of triethylene diamine, tetramethylguanidine and sodium carbonate into an anhydrous dye bath, wherein the weight ratio of the triethylene diamine to the tetramethylguanidine to the sodium carbonate is 1.5: 1: 0.1. the addition of the fixing base was 6 g/L. And (5) dyeing for 5 h. And after dyeing is finished, cooling to room temperature, alternately washing 3 times by using ethylene glycol monomethyl ether acetate at 50 ℃ and dimethyl sulfoxide at 50 ℃, wherein the dosage of each time is 20mL, and finally drying to obtain the dyed cotton fabric.
Example 5
A reactive black dye composition was prepared by mixing 65% of the dye compound represented by the formula (I-1), 25% of the dye compound represented by the formula (II-1) and 10% of the dye compound represented by the formula (III-1). Dissolving a reactive black dye composition in a solvent with a volume ratio of 70: and (3) obtaining a dye bath from 30 parts of ethylene glycol monomethyl ether acetate and dimethyl sulfoxide in an anhydrous solvent. Then adding triethylene diamine into an anhydrous dye bath; the amount added was 6 g/L. And (4) carrying out ultrasonic treatment to obtain a uniform anhydrous dye bath. Placing the cotton fabric which is swelled by dimethyl sulfoxide in advance and has swelling degree of 22% into an anhydrous dye bath. The bath ratio of the cotton fabric to the anhydrous dye bath is 1: 16 g/mL. The dye amount was 4 o.w.f%. Heating at the speed of 3 ℃/min, keeping the temperature after the target temperature is reached to 85 ℃, and dyeing for 5 hours; and after dyeing is finished, cooling to room temperature, alternately washing 3 times by using ethylene glycol monomethyl ether acetate at 50 ℃ and dimethyl sulfoxide at 50 ℃, wherein the dosage of each time is 20mL, and finally drying to obtain the dyed cotton fabric.
Example 6
A reactive black dye composition was prepared by mixing 65% of the dye compound represented by the formula (I-1), 25% of the dye compound represented by the formula (II-1) and 10% of the dye compound represented by the formula (III-1). Dissolving a reactive black dye composition in a solvent with a volume ratio of 70: and (3) obtaining a dye bath from 30 parts of ethylene glycol monomethyl ether acetate and dimethyl sulfoxide in an anhydrous solvent. Then tetramethylguanidine was added in an amount of 6 g/L. And (4) carrying out ultrasonic treatment to obtain a uniform anhydrous dye bath. Placing the cotton fabric which is swelled by dimethyl sulfoxide in advance and has swelling degree of 22% into an anhydrous dye bath. The bath ratio of the cotton fabric to the anhydrous dye bath is 1: 16 g/mL. The dye amount was 4 o.w.f%. Heating at the speed of 3 ℃/min, keeping the temperature after the target temperature is reached to 85 ℃, and dyeing for 5 hours; and after dyeing is finished, cooling to room temperature, alternately washing 3 times by using ethylene glycol monomethyl ether acetate at 50 ℃ and dimethyl sulfoxide at 50 ℃, wherein the dosage of each time is 20mL, and finally drying to obtain the dyed cotton fabric.
Comparative example 1
The same as in example 1 was repeated except that the reactive black dye composition was replaced with 100% of the dye compound represented by the formula (I-1).
Comparative example 2
The same as in example 1 except that ethylene glycol monomethyl ether acetate was replaced with ethylene glycol dimethyl ether.
Comparative example 3
The procedure is as in example 1 except that no fixing base is added.
Comparative example 4
The reactive black dye composition was replaced with 100% of the dye compound represented by the formula (I-2), and dissolved in water to prepare a 2.5g/L dye bath. The dried cotton fabric was placed directly into the dye bath. The bath ratio of the cotton fabric to the dye bath is 1: 16 g/mL. The dye amount was 4 o.w.f%. Adding 15% anhydrous sodium sulfate at 30 deg.C, and maintaining the temperature for 60 min. Then the temperature was raised to 60 ℃ at a rate of 3 ℃/min and the dye was blotted for 45 min. Then adding sodium carbonate with the total amount equivalent to 20g/L in two batches for fixation, wherein the total fixation time is 60 min. And taking out the dyed fabric, washing with water, boiling in 3g/L soap solution for 15min, and finally drying to obtain the dyed cotton fabric.
The Integ values and the two fixation degrees of examples 1-6 and comparative examples 1-4 were determined according to the method of the invention as described previously. See table 1 for results.
TABLE 1
The rubbing fastness and washing fastness (60 ℃) of examples 1 to 6 and comparative examples 1 to 4 were measured according to the method of the present invention as described previously. See table 2 for results.
TABLE 2
As can be seen from tables 1 and 2, examples 1 to 3 relate to a dyeing method in which dyeing and fixation are carried out simultaneously, and due to the adoption of specific reactive dyes, anhydrous solvents and fixation bases, the effect of high black can be achieved, and the high fixation rate and the high dyeing fastness are achieved. Example 4 relates to a dyeing process with dye-fixing carried out in steps, which is comparable to examples 1 to 3. Examples 5-6 use a single fixing base, although the jetness and the fastness of dyeing are slightly lower than examples 1-4, but still significantly higher than the existing bath dyeing process; furthermore, the fixation yield is comparable to the prior art. Comparative example 1 was conducted to confirm that the increase in value of integer values of examples 1 to 6 was mainly due to the synergistic effect of the three dye components of the reactive black dye composition. Comparative examples 2 and 3 were used to demonstrate the role of a particular solvent and fixing base, respectively, in the present invention. Comparative example 4 represents a prior art water bath dyeing process.
The above description is only a preferred embodiment of the present invention and is not intended to limit the present invention, and various modifications and changes may be made by those skilled in the art. Any modification, equivalent replacement, or improvement made within the spirit and principle of the present invention shall fall within the protection scope of the present invention.
Claims (8)
1. A waterless dyeing method for dyeing and fixing dark-tone cotton fabric step by step comprises the following steps: placing the cotton fabric in an anhydrous dye bath, heating at a certain speed, keeping the temperature after reaching a target temperature, and dyeing for a certain time; cooling to room temperature after dyeing is finished, cleaning the dyed fabric by using an anhydrous solvent, and finally drying to obtain a dyed cotton fabric; wherein the anhydrous dye bath is obtained by dissolving a reactive dye in an anhydrous solvent, and the reactive dye is selected from a reactive black dye composition; the method is characterized by further adding a fixation base mainly comprising an organic base into the anhydrous dye bath after the target temperature is reached; by "consisting essentially of" is meant that the weight of the organic base is greater than 90% of the sum of the weight of all the fixing bases;
the reactive black dye composition consists of a dye compound A, a dye compound B and a dye compound C; wherein,
the dye compound A is selected from any one or more of dye compounds shown in a formula (I);
In the formula (I), R1-R4Each independently selected from H, C1-C4Alkyl radical, C1-C4Alkoxy and SO3M;Y1-Y2Each independently selected from SO2CH=CH2Or SO2CH2CH2OSO3M; m is selected from H, Na or K;
the dye compound B is selected from any one or more of dye compounds shown in a formula (II);
in the formula (II), R5-R8Each independently selected from H, C1-C4Alkyl radical, C1-C4Alkoxy and SO3M;Y3-Y4Each independently selected from SO2CH=CH2Or SO2CH2CH2OSO3M; m is selected from H, Na or K;
the dye compound C is selected from any one or more of dye compounds shown in a formula (III);
in the formula (III), R9-R10Each independently selected from H, C1-C4Alkyl radical, C1-C4Alkoxy and SO3M;Y5Independently selected from SO2CH=CH2Or SO2CH2CH2OSO3M; m is selected from H, Na or K;
the weight percentage of the dye compound A is 50-80 percent based on the total weight of the reactive black dye composition; the weight percentage of the dye compound B is 15-35%; the weight percentage of the dye compound C is 5-18%;
the organic base is selected from a mixture of triethylene diamine and tetramethyl guanidine; the weight ratio of triethylene diamine to tetramethyl guanidine is (1.5-2): 1;
the anhydrous solvent consists of ethylene glycol monomethyl ether acetate and an aprotic polar solvent; the volume ratio of the ethylene glycol monomethyl ether acetate to the aprotic polar solvent is (55-80): (45-20).
5. the waterless dyeing method according to claim 1, wherein the weight percentage of dye compound a is 60-70% based on the total weight of the reactive black dye composition; the weight percentage of the dye compound B is 22-28%; the weight percentage of the dye compound C is 8-12%.
6. The waterless dyeing method of claim 1, wherein the fixing base is selected from a mixture of triethylenediamine, tetramethylguanidine, and sodium carbonate.
7. The waterless dyeing method according to claim 6, wherein the weight ratio of triethylenediamine, tetramethylguanidine and sodium carbonate is (1.5-1.7): 1: (0.01-0.15).
8. The waterless dyeing method according to claim 1, wherein the cotton fabric is previously subjected to dimethyl sulfoxide swelling.
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