EP0036537B1 - Procédé de teinture de mélanges de fibres de polyester et de cellulose - Google Patents
Procédé de teinture de mélanges de fibres de polyester et de cellulose Download PDFInfo
- Publication number
- EP0036537B1 EP0036537B1 EP81101670A EP81101670A EP0036537B1 EP 0036537 B1 EP0036537 B1 EP 0036537B1 EP 81101670 A EP81101670 A EP 81101670A EP 81101670 A EP81101670 A EP 81101670A EP 0036537 B1 EP0036537 B1 EP 0036537B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- dyeing
- polyester
- cellulose
- phosphate
- dyestuff
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 238000004043 dyeing Methods 0.000 title claims description 14
- 238000000034 method Methods 0.000 title claims description 14
- 229920000728 polyester Polymers 0.000 title claims description 10
- 239000000203 mixture Substances 0.000 title claims description 8
- 239000000835 fiber Substances 0.000 title description 5
- 229920002678 cellulose Polymers 0.000 title description 3
- 239000001913 cellulose Substances 0.000 title description 3
- 239000000975 dye Substances 0.000 claims description 14
- 239000002253 acid Substances 0.000 claims description 7
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 claims description 4
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 claims description 3
- 229920003043 Cellulose fiber Polymers 0.000 claims description 2
- 239000001488 sodium phosphate Substances 0.000 claims description 2
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 claims description 2
- 229910000406 trisodium phosphate Inorganic materials 0.000 claims description 2
- 235000019801 trisodium phosphate Nutrition 0.000 claims description 2
- SOBHUZYZLFQYFK-UHFFFAOYSA-K trisodium;hydroxy-[[phosphonatomethyl(phosphonomethyl)amino]methyl]phosphinate Chemical compound [Na+].[Na+].[Na+].OP(O)(=O)CN(CP(O)([O-])=O)CP([O-])([O-])=O SOBHUZYZLFQYFK-UHFFFAOYSA-K 0.000 claims 1
- 239000000985 reactive dye Substances 0.000 description 7
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 239000000986 disperse dye Substances 0.000 description 3
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 2
- XSIFPSYPOVKYCO-UHFFFAOYSA-N butyl benzoate Chemical compound CCCCOC(=O)C1=CC=CC=C1 XSIFPSYPOVKYCO-UHFFFAOYSA-N 0.000 description 2
- VXIVSQZSERGHQP-UHFFFAOYSA-N chloroacetamide Chemical compound NC(=O)CCl VXIVSQZSERGHQP-UHFFFAOYSA-N 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- -1 difluorochloropyrimidinyl residue Chemical group 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 238000009981 jet dyeing Methods 0.000 description 2
- 150000002596 lactones Chemical class 0.000 description 2
- UFFAFBPZFGAMJJ-UHFFFAOYSA-N (2-methoxy-4,6-dimethylphenyl)boronic acid Chemical compound COC1=CC(C)=CC(C)=C1B(O)O UFFAFBPZFGAMJJ-UHFFFAOYSA-N 0.000 description 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- RELMFMZEBKVZJC-UHFFFAOYSA-N 1,2,3-trichlorobenzene Chemical compound ClC1=CC=CC(Cl)=C1Cl RELMFMZEBKVZJC-UHFFFAOYSA-N 0.000 description 1
- YOHJPFQGGNEGSE-UHFFFAOYSA-N 1-diethoxyphosphorylethanone Chemical compound CCOP(=O)(C(C)=O)OCC YOHJPFQGGNEGSE-UHFFFAOYSA-N 0.000 description 1
- ZOXHFYPCZQICQD-UHFFFAOYSA-N 2,2-dichloroacetic acid;sodium Chemical compound [Na].OC(=O)C(Cl)Cl ZOXHFYPCZQICQD-UHFFFAOYSA-N 0.000 description 1
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- ATACSYDDCNWCLV-UHFFFAOYSA-N 2-chloroacetic acid;sodium Chemical compound [Na].OC(=O)CCl ATACSYDDCNWCLV-UHFFFAOYSA-N 0.000 description 1
- MHGOKSLTIUHUBF-UHFFFAOYSA-N 2-ethylhexyl sulfate Chemical compound CCCCC(CC)COS(O)(=O)=O MHGOKSLTIUHUBF-UHFFFAOYSA-N 0.000 description 1
- WAVYAFBQOXCGSZ-UHFFFAOYSA-N 2-fluoropyrimidine Chemical compound FC1=NC=CC=N1 WAVYAFBQOXCGSZ-UHFFFAOYSA-N 0.000 description 1
- ZTHQBROSBNNGPU-UHFFFAOYSA-N Butyl hydrogen sulfate Chemical compound CCCCOS(O)(=O)=O ZTHQBROSBNNGPU-UHFFFAOYSA-N 0.000 description 1
- KKUKTXOBAWVSHC-UHFFFAOYSA-N Dimethylphosphate Chemical compound COP(O)(=O)OC KKUKTXOBAWVSHC-UHFFFAOYSA-N 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- HVWGGPRWKSHASF-UHFFFAOYSA-N Sulfuric acid, monooctadecyl ester Chemical compound CCCCCCCCCCCCCCCCCCOS(O)(=O)=O HVWGGPRWKSHASF-UHFFFAOYSA-N 0.000 description 1
- 241001584775 Tunga penetrans Species 0.000 description 1
- JAWMENYCRQKKJY-UHFFFAOYSA-N [3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-ylmethyl)-1-oxa-2,8-diazaspiro[4.5]dec-2-en-8-yl]-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]methanone Chemical compound N1N=NC=2CN(CCC=21)CC1=NOC2(C1)CCN(CC2)C(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F JAWMENYCRQKKJY-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- BVXOPEOQUQWRHQ-UHFFFAOYSA-N dibutyl phosphite Chemical compound CCCCOP([O-])OCCCC BVXOPEOQUQWRHQ-UHFFFAOYSA-N 0.000 description 1
- LXCYSACZTOKNNS-UHFFFAOYSA-N diethoxy(oxo)phosphanium Chemical compound CCO[P+](=O)OCC LXCYSACZTOKNNS-UHFFFAOYSA-N 0.000 description 1
- ATLPLEZDTSBZQG-UHFFFAOYSA-L dioxido-oxo-propan-2-yl-$l^{5}-phosphane Chemical compound CC(C)P([O-])([O-])=O ATLPLEZDTSBZQG-UHFFFAOYSA-L 0.000 description 1
- NFORZJQPTUSMRL-UHFFFAOYSA-N dipropan-2-yl hydrogen phosphite Chemical compound CC(C)OP(O)OC(C)C NFORZJQPTUSMRL-UHFFFAOYSA-N 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
- 229940043264 dodecyl sulfate Drugs 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000003977 halocarboxylic acids Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- LPTIRUACFKQDHZ-UHFFFAOYSA-N hexadecyl sulfate;hydron Chemical compound CCCCCCCCCCCCCCCCOS(O)(=O)=O LPTIRUACFKQDHZ-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 235000010292 orthophenyl phenol Nutrition 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical class N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- LIOTZBNOJXQXIL-UHFFFAOYSA-M sodium;3-chloropropanoate Chemical compound [Na+].[O-]C(=O)CCCl LIOTZBNOJXQXIL-UHFFFAOYSA-M 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- VWBIJLFTDUZNDF-UHFFFAOYSA-J tetrasodium hydrogen phosphate Chemical compound [Na+].[Na+].[Na+].[Na+].OP([O-])([O-])=O.OP([O-])([O-])=O VWBIJLFTDUZNDF-UHFFFAOYSA-J 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 125000000101 thioether group Chemical group 0.000 description 1
- DQWPFSLDHJDLRL-UHFFFAOYSA-N triethyl phosphate Chemical compound CCOP(=O)(OCC)OCC DQWPFSLDHJDLRL-UHFFFAOYSA-N 0.000 description 1
- WVLBCYQITXONBZ-UHFFFAOYSA-N trimethyl phosphate Chemical compound COP(=O)(OC)OC WVLBCYQITXONBZ-UHFFFAOYSA-N 0.000 description 1
- MGEISCKTUGVOHN-UHFFFAOYSA-N tris(2-hydroxyethyl) phosphate Chemical compound OCCOP(=O)(OCCO)OCCO MGEISCKTUGVOHN-UHFFFAOYSA-N 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
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
- 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
- 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
- D06P3/82—Textiles which contain different kinds of fibres
- D06P3/8204—Textiles which contain different kinds of fibres fibres of different chemical nature
- D06P3/8223—Textiles which contain different kinds of fibres fibres of different chemical nature mixtures of fibres containing hydroxyl and ester groups
- D06P3/8238—Textiles which contain different kinds of fibres fibres of different chemical nature mixtures of fibres containing hydroxyl and ester groups using different kinds of dye
- D06P3/8252—Textiles which contain different kinds of fibres fibres of different chemical nature mixtures of fibres containing hydroxyl and ester groups using different kinds of dye using dispersed and reactive dyes
Definitions
- the invention relates to a process for single-bath, single-stage dyeing of polyester / cellulose fiber mixtures by the exhaust process using a dye bath which, in addition to a disperse dye, contains a reactive dye and 0.1 to 5 g / l of an acid donor effective at the dyeing temperature.
- the process is characterized in that a reactive dye having a fluorotriazinyl or fluoropyrimidinyl group is used as the reactive dye and the starting pH of the dyebath is adjusted by adding disodium hydrogen phosphate or a trisodium phosphate / monosodium dihydrogen phosphate mixture.
- DE-A-1 819464 discloses a process for dyeing mixtures of cellulose and polyester fibers with reactive and disperse dyes, in addition to the above-mentioned dyes, alkalis and halogen-containing organic compounds acting as acid donors and, if appropriate, carriers customary for dyeing polyester fibers Dye bath are included.
- Suitable reactive dyes in the process according to the invention are, in particular, organic dyes from the anthraquinone, azo and phthalocyanine series which have a monofluoro-s-triazinyl radical, in particular those which contain an ether or thioether group or in particular an optionally substituted amino group as further substituents on the triazine ring or else fluoropyrimidine dyes, especially those with a difluorochloropyrimidinyl residue.
- Such dyes are described in large numbers, for example in British Patents 1,169,254; 1 108 606; 1 526840.
- Water-soluble derivatives of organic or inorganic acids are used as acid donors, which release acidic groups specifically in the temperature range from 60 to 100 ° C and thus the pH value of the initially neutral to weakly alkaline dye bath during the dyeing process in the acidic range, preferably up to pH Move 4-5.
- Half esters of sulfuric acid such as lauryl sulfate, hexadecyl sulfate or octadecyl sulfate and preferably 2-ethylhexyl sulfate, butyl sulfate, and the sulfuric acid esters of oxyethylated and oxypropylated alcohols such as.
- trimethyl phosphate triethyl phosphate, tris (hydroxyethyl) phosphate, dimethyl phosphate, diethyl phosphite, dipropyl phosphite, di-isopropyl phosphite, dibutyl phosphite, dimethyl methanephosphonate, Ethanphosphonklarediethylester, Phosphonopropionchuretrimethylester, Cyanethanphosphonklaredimethylester, Cyanmethanphosphonklaredimethylester, and hydroxyethane Hydroxymethanphosphonklaredimethylester, 2-Chlorethanphosphonklaredimethylester, 2-Chlorethanphosphonklathylester, Acetylphosphonklaredimethylester and diethyl acetylphosphonate and tetramethyl phosphonosuccinate.
- polyester fiber components may be used for the dyeing of the polyester fiber components.
- examples include trichlorobenzene, o-dichlorobenzene, methyl cresotlonate, butyl benzoate, o-phenylphenol, p-phenylphenol.
- the carriers are used in the usual amounts for dyeing polyester fibers and are added to the dye bath after the dye and salt have been added.
- the process is suitable for dyeing yarn and pieces on packing and cross-winding machines, jet dyeing machines, reel runners and jiggers.
- the process is generally carried out as follows:
- the textile material is introduced into a dyebath which has a pH of about 7-10, preferably 7-9 and 0.01-10 g / 1 of a fluorotriazinyl and / or fluoropyrimidinyl reactive dye , 01 ⁇ 10 g / l of a conventional disperse dye, 10-200 g / l of a conventional electrolyte such as sodium sulfate or sodium chloride, 0.1 ⁇ 5 g / l of an acid dispenser and 0.1-10 g / l disodium monohydrogen phosphate or trisodium phosphate monosodium dihydrogen phosphate Mixture and other conventional auxiliaries, for example 1-8 g / 1 of a carrier contains.
- the dyebath is heated from 30-40 ° C to 95-130 ° C within 1-2 hours and dyed at this temperature for 2-1 hours.
- the reactive dye is dyed in the alkaline range, preferably at pH 7.5-9 below 100 ° C.
- the amount of acid donor is measured so that after dyeing the pH is below 7, preferably in the range 4-5.
- 100 of a knitted fabric consisting of 50 g polyester and 50 g cotton are treated on a HT jet dyeing machine with a 30 ° C. liquor, which consists of consists.
- the liquor is brought to 130 ° C. in 100 minutes and kept at this temperature for 1 hour.
- the liquor is brought to 130 ° C. in 100 minutes and kept at this temperature for 1 hour.
- 100 g of a knitted fabric consisting of 50 g polyester and 50 g mercerized cotton are treated at 75 ° C. for 45 minutes on a HT tree dyeing machine with a liquor which consists of consists.
- the liquor is brought to 130 ° C. in 55 minutes and kept at this temperature for 1 hour.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Coloring (AREA)
Claims (2)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19803010979 DE3010979A1 (de) | 1980-03-21 | 1980-03-21 | Faerbeverfahren |
DE3010979 | 1980-03-21 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0036537A2 EP0036537A2 (fr) | 1981-09-30 |
EP0036537A3 EP0036537A3 (en) | 1981-12-16 |
EP0036537B1 true EP0036537B1 (fr) | 1983-09-28 |
Family
ID=6097954
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP81101670A Expired EP0036537B1 (fr) | 1980-03-21 | 1981-03-07 | Procédé de teinture de mélanges de fibres de polyester et de cellulose |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP0036537B1 (fr) |
JP (1) | JPS5846594B2 (fr) |
DE (2) | DE3010979A1 (fr) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104074069A (zh) * | 2014-07-02 | 2014-10-01 | 浙江航民股份有限公司 | 染色用分散染料与活性染料的同浴剂 |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3115069A1 (de) * | 1981-04-14 | 1982-11-04 | Bayer Ag, 5090 Leverkusen | Faerbeverfahren |
JPS5930971A (ja) * | 1982-07-06 | 1984-02-18 | 日本化薬株式会社 | セルロ−ス及びセルロ−ス含有繊維材料の捺染又はパジング染色法 |
JPS59106583A (ja) * | 1982-12-13 | 1984-06-20 | 日本化学工業株式会社 | ポリエステル/セルロ−ス混紡繊維品の染色方法 |
JPS6253376A (ja) * | 1985-09-03 | 1987-03-09 | Nippon Chem Ind Co Ltd:The | 染料組成物 |
JPH0684593B2 (ja) * | 1985-09-15 | 1994-10-26 | 一方社油脂工業株式会社 | ポリエステル/セルロ−ス混紡・交織品の染色方法 |
JPS62230858A (ja) * | 1985-12-27 | 1987-10-09 | Nippon Chem Ind Co Ltd:The | 染料組成物 |
DE4237883A1 (de) * | 1992-11-10 | 1994-05-11 | Bayer Ag | Reaktivfarbstoffmischung für Polyester/Cellulosefasermischungen |
TW330957B (en) * | 1995-06-22 | 1998-05-01 | Daistar Japan Kk | Method of dyeing a blended fiber containing cellulose fibers and polyester fibers |
CN102561071B (zh) * | 2010-12-23 | 2014-04-09 | 福建凤竹纺织科技股份有限公司 | 一种涤棉织物的分散、活性一浴染色工艺 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1469750B2 (de) * | 1965-12-31 | 1973-12-06 | Farbwerke Hoechst Ag, Vormals Meister Lucius & Bruening, 6000 Frankfurt | Verfahren zum Farben von Fasermateriahen aus nativer oder regene nerter Cellulose mit Reaktivfarb stoffen oder von Gemischen aus diesen Cellulosefasern und Fasermateriahen aus hochmolekularen linearen Poly estern mit Reaktivfarbstoffen und Dis persionsfarbstoffen |
DE1619464A1 (de) * | 1966-02-23 | 1970-10-29 | Hoechst Ag | Verfahren zum Faerben von Cellulosefasern mit Reaktivfarbstoffen oder von Mischungen aus Cellulose- und Polyesterfasern mit Reaktiv- und Dispersionsfarbstoffen |
US3910758A (en) * | 1971-06-17 | 1975-10-07 | Bayer Ag | Dyeing wool with fluorine substituted pyrimidine containing azo reactive dyestuff |
US3980428A (en) * | 1972-11-06 | 1976-09-14 | Sandoz Ltd. | Dyeing process |
DE2835035B2 (de) * | 1978-08-10 | 1980-10-09 | Hoechst Ag, 6000 Frankfurt | Verfahren zum Färben von Cellulosefasern mit Reaktivfarbstoffen nach der Ausziehmethode |
DE2834997C2 (de) * | 1978-08-10 | 1980-08-28 | Hoechst Ag, 6000 Frankfurt | Verfahren zum Färben von synthetischen Polyamidfasern mit Reaktivfarbstoffen nach der Ausziehmethode |
DE2913718B2 (de) * | 1979-04-05 | 1981-02-05 | Bayer Ag, 5090 Leverkusen | Verfahren zum Färben von Cellulosefasern und Cellulosefasern enthaltenden Fasermischungen mit Reaktivfarbstoffen |
DE2933343A1 (de) * | 1979-08-17 | 1981-03-26 | Bayer Ag, 51373 Leverkusen | Faerben von wolle/cellulosefasermischungen |
-
1980
- 1980-03-21 DE DE19803010979 patent/DE3010979A1/de not_active Withdrawn
-
1981
- 1981-03-07 DE DE8181101670T patent/DE3160995D1/de not_active Expired
- 1981-03-07 EP EP81101670A patent/EP0036537B1/fr not_active Expired
- 1981-03-18 JP JP56038027A patent/JPS5846594B2/ja not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104074069A (zh) * | 2014-07-02 | 2014-10-01 | 浙江航民股份有限公司 | 染色用分散染料与活性染料的同浴剂 |
Also Published As
Publication number | Publication date |
---|---|
EP0036537A2 (fr) | 1981-09-30 |
JPS56144277A (en) | 1981-11-10 |
DE3010979A1 (de) | 1981-10-01 |
DE3160995D1 (en) | 1983-11-03 |
EP0036537A3 (en) | 1981-12-16 |
JPS5846594B2 (ja) | 1983-10-17 |
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