EP0036537A2 - 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
- EP0036537A2 EP0036537A2 EP81101670A EP81101670A EP0036537A2 EP 0036537 A2 EP0036537 A2 EP 0036537A2 EP 81101670 A EP81101670 A EP 81101670A EP 81101670 A EP81101670 A EP 81101670A EP 0036537 A2 EP0036537 A2 EP 0036537A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- acid
- dyeing
- dye
- polyester
- 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.)
- Granted
Links
- 238000000034 method Methods 0.000 title claims abstract description 15
- 238000004043 dyeing Methods 0.000 title claims abstract description 14
- 229920000728 polyester Polymers 0.000 title claims abstract description 9
- 239000000203 mixture Substances 0.000 title claims abstract description 5
- 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 abstract description 16
- 239000002253 acid Substances 0.000 claims abstract description 8
- 229920003043 Cellulose fiber Polymers 0.000 claims abstract 2
- 239000000985 reactive dye Substances 0.000 claims description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 4
- 239000000986 disperse dye Substances 0.000 claims description 3
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
- 150000001408 amides Chemical class 0.000 claims description 2
- 150000003977 halocarboxylic acids Chemical class 0.000 claims description 2
- 150000002596 lactones Chemical class 0.000 claims description 2
- 239000008363 phosphate buffer Substances 0.000 claims description 2
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 claims description 2
- 239000003513 alkali Substances 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 150000002894 organic compounds Chemical class 0.000 claims 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical class OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims 1
- 159000000000 sodium salts Chemical class 0.000 claims 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 abstract description 2
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 abstract 1
- 239000001488 sodium phosphate Substances 0.000 abstract 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 abstract 1
- 229910000406 trisodium phosphate Inorganic materials 0.000 abstract 1
- 235000019801 trisodium phosphate Nutrition 0.000 abstract 1
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-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
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- -1 alkali metal salts 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
- 239000000872 buffer Substances 0.000 description 2
- XSIFPSYPOVKYCO-UHFFFAOYSA-N butyl benzoate Chemical compound CCCCOC(=O)C1=CC=CC=C1 XSIFPSYPOVKYCO-UHFFFAOYSA-N 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 238000009981 jet dyeing Methods 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
- ZOXHFYPCZQICQD-UHFFFAOYSA-N 2,2-dichloroacetic acid;sodium Chemical compound [Na].OC(=O)C(Cl)Cl ZOXHFYPCZQICQD-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
- 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
- 229910052783 alkali metal 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
- 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
- 229930188620 butyrolactone Natural products 0.000 description 1
- VXIVSQZSERGHQP-UHFFFAOYSA-N chloroacetamide Chemical compound NC(=O)CCl VXIVSQZSERGHQP-UHFFFAOYSA-N 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
- CZHYKKAKFWLGJO-UHFFFAOYSA-N dimethyl phosphite Chemical compound COP([O-])OC CZHYKKAKFWLGJO-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
- 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
- 235000010292 orthophenyl phenol Nutrition 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
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 fiber mixtures of cellulose and polyester fibers with reactive and disperse dyes by the pull-out process from electrolyte-containing dye baths, characterized in that a dye bath is used which contains a reactive dye with fluorotriazinyl and / or Fluoropyrimidinyl group and 0.1 - 5 g / 1 of an acid donor effective at dyeing temperature.
- Suitable reactive dyes are, in particular, organic dyes from the anthraquinone, azo and phthalocanine 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 Difluorchlorpyrimidinylrest.
- Such dyes are described in large numbers, for example. in British Patents 1,169,254; 1,188,606; 1 526 840.
- 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 dye bath, which is initially neutral to weakly alkaline during the dyeing process, preferably up to pH in the acidic range Move 4-5.
- Suitable acid donors are: alkali metal salts of halocarboxylic acids and their amides, such as sodium monochloroacetic acid, sodium dichloroacetic acid, sodium 3-chloropropionate, monochloroacetamide; Lactones such as butyrolactone; Halbester of sulfuric acid such as lauryl sulfate, hexadecyl sulfate and octadecyl sulfate or preferably 2-ethylhexyl sulfate, butyl sulfate, as well as the oxyethylated and oxypropylated Schwefelklasteder of alcohols, for example butylglycol sulfate, Butyldiglykolsulfat, further C 1 -C 4 alkyl esters of phosphoric acid or phosphorous acid, C 1 -C 4 alkyl esters of phosphonic and phosphinic acid, such as trimethyl phosphate, trie
- polyester fiber components Commercially available carriers may be used for the dyeing of the polyester fiber components. Examples include trichlorobenzene, o-dichlorobenzene, methyl cresotate, 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 packers and packages, 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, 0.1-10 g / l of an acid donor and preferably 0.1-10 g / l of a buffer, in particular one Contains phosphate buffers for a pH range of 7-9, as well as other common auxiliaries, for example 1-8 g / l of a carrier.
- the dye bath is inside heated from 30 - 40 ° C to 95 - 130 ° C for 1 - 2 hours and dyed at this temperature for 1/2 - 1 hour.
- Suitable buffer systems are, for example, trisodium phosphate monosodium dihydrogen phosphate or disodium hydrogen phosphate.
- the reactive dye is dyed in the alkaline range, preferably at pH 7.5-9 below 100 ° C.
- 100 g 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.
- 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)
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 true EP0036537A2 (fr) | 1981-09-30 |
| EP0036537A3 EP0036537A3 (en) | 1981-12-16 |
| EP0036537B1 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 (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0062865A1 (fr) * | 1981-04-14 | 1982-10-20 | Bayer Ag | Procédé de teinture |
| EP0597330A1 (fr) * | 1992-11-10 | 1994-05-18 | Bayer Ag | Composition de colorants réactifs pour mélanges de fibres polyester/cellulose |
| CN102561071A (zh) * | 2010-12-23 | 2012-07-11 | 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 |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| TW330957B (en) * | 1995-06-22 | 1998-05-01 | Daistar Japan Kk | Method of dyeing a blended fiber containing cellulose fibers and polyester fibers |
| 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 |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1469750A1 (de) * | 1965-12-31 | 1968-12-12 | Hoechst Ag | Verfahren zum Faerben von Fasermaterialien aus nativer oder regenerierter Cellulose mit Reaktivfarbstoffen oder von Gemischen aus diesen Cellulosefasern und Fasermaterialien aus hochmolekularen linearen Polyestern mit Reaktivfarbstoffen und Dispersionsfarbstoffen |
| 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 |
| DE2354728A1 (de) * | 1972-11-06 | 1974-05-09 | Sandoz Ag | Verfahren zum faerben und fixieren von textilen materialien |
| US3910758A (en) * | 1971-06-17 | 1975-10-07 | Bayer Ag | Dyeing wool with fluorine substituted pyrimidine containing azo reactive dyestuff |
| DE2834997B1 (de) * | 1978-08-10 | 1980-01-03 | Hoechst Ag | Verfahren zum Faerben von synthetischen Polyamidfasern mit Reaktivfarbstoffen nach der Ausziehmethode |
| GB2027756A (en) * | 1978-08-10 | 1980-02-27 | Hoechst Ag | Process for dyeing cellulose fibres with reactive dyes according to the batchwise exhaustion method |
| EP0017172A1 (fr) * | 1979-04-05 | 1980-10-15 | Bayer Ag | Procédé de teinture de fibres cellulosiques et de mélanges fibreux contenant des fibres cellulosiques et de polyesters avec des colorants réactifs |
| EP0024332A1 (fr) * | 1979-08-17 | 1981-03-04 | Bayer Ag | Teinture de mélanges de fibres de laine et de fibres cellulosiques |
-
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
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1469750A1 (de) * | 1965-12-31 | 1968-12-12 | Hoechst Ag | Verfahren zum Faerben von Fasermaterialien aus nativer oder regenerierter Cellulose mit Reaktivfarbstoffen oder von Gemischen aus diesen Cellulosefasern und Fasermaterialien aus hochmolekularen linearen Polyestern mit Reaktivfarbstoffen und Dispersionsfarbstoffen |
| 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 |
| DE2354728A1 (de) * | 1972-11-06 | 1974-05-09 | Sandoz Ag | Verfahren zum faerben und fixieren von textilen materialien |
| DE2834997B1 (de) * | 1978-08-10 | 1980-01-03 | Hoechst Ag | Verfahren zum Faerben von synthetischen Polyamidfasern mit Reaktivfarbstoffen nach der Ausziehmethode |
| GB2027756A (en) * | 1978-08-10 | 1980-02-27 | Hoechst Ag | Process for dyeing cellulose fibres with reactive dyes according to the batchwise exhaustion method |
| EP0017172A1 (fr) * | 1979-04-05 | 1980-10-15 | Bayer Ag | Procédé de teinture de fibres cellulosiques et de mélanges fibreux contenant des fibres cellulosiques et de polyesters avec des colorants réactifs |
| EP0024332A1 (fr) * | 1979-08-17 | 1981-03-04 | Bayer Ag | Teinture de mélanges de fibres de laine et de fibres cellulosiques |
Non-Patent Citations (1)
| Title |
|---|
| CHEMICAL ABSTRACTS, Band 90, Nr. 20, 14. Mai 1979, seite 53, zusammenfassung 153.370d Columbus Ohio (US) & Cellul. Chem. Technol. 1978, 12(6) 693-702 A. BENDAK et al. "New Processing Technique for Dyeing of Polyester/Cotton Blend" * Abstract * * |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0062865A1 (fr) * | 1981-04-14 | 1982-10-20 | Bayer Ag | Procédé de teinture |
| EP0597330A1 (fr) * | 1992-11-10 | 1994-05-18 | Bayer Ag | Composition de colorants réactifs pour mélanges de fibres polyester/cellulose |
| CN102561071A (zh) * | 2010-12-23 | 2012-07-11 | 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 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0036537B1 (fr) | 1983-09-28 |
| 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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