EP0023660A2 - Procédé pour produire des effets de réserve sur des mélanges de fibres de polyester et de fibres cellulosiques - Google Patents

Procédé pour produire des effets de réserve sur des mélanges de fibres de polyester et de fibres cellulosiques Download PDF

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Publication number
EP0023660A2
EP0023660A2 EP80104279A EP80104279A EP0023660A2 EP 0023660 A2 EP0023660 A2 EP 0023660A2 EP 80104279 A EP80104279 A EP 80104279A EP 80104279 A EP80104279 A EP 80104279A EP 0023660 A2 EP0023660 A2 EP 0023660A2
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EP
European Patent Office
Prior art keywords
alkali
dye
reactive
alkaline
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
Application number
EP80104279A
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German (de)
English (en)
Other versions
EP0023660A3 (en
EP0023660B1 (fr
Inventor
Erich Dr. Feess
Friedrich Dr. Reinhardt
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hoechst AG
Original Assignee
Hoechst AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Hoechst AG filed Critical Hoechst AG
Publication of EP0023660A2 publication Critical patent/EP0023660A2/fr
Publication of EP0023660A3 publication Critical patent/EP0023660A3/de
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Publication of EP0023660B1 publication Critical patent/EP0023660B1/fr
Expired legal-status Critical Current

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Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P5/00Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
    • D06P5/15Locally discharging the dyes
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P5/00Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
    • D06P5/12Reserving parts of the material before dyeing or printing ; Locally decreasing dye affinity by chemical means

Definitions

  • the same difficulties also stand in the way of developing an etching or reserve printing process.
  • the invention was therefore based on the object of producing white and colored reserves on mixed materials composed of polyester and cellulose fibers.
  • This object is achieved in that a mixture of a slightly acidic preparation is applied to the mixing material, the at least one etchable reactive dye which stains both types of fibers, or a mixture of at least one etchable reactive dye and at least one disperse dye which is mixed with alkali in a water-soluble anionic Form can be transferred, and possibly contains a neutral fixing aid for reactive dyes, then prints on a paste that contains alkali and a reducing agent, whereupon fixation with superheated steam or saturated steam in conjunction with hot air takes place, and, if the acidic preparation is not the neutral Contains fixative, a treatment with alkaline agents and a steaming process.
  • White reserves are obtained by this process.
  • vat dyes, alkali-stable or viable disperse dyes or a combination of such dyes are added to the alkaline printing paste.
  • conversion articles can also be produced if non-etchable dyes are added to the acidic preparation.
  • the substrates colored according to the invention comprise mixed materials composed of polyester fibers, in particular polyethylene glycol terephthalate fibers, and natural and regenerated cellulose fibers in all usual mixing ratios.
  • the slightly acidic preparation is expediently applied by padding or splashing, but also by printing, in particular when large-area patterns (decks) are pre-printed.
  • the embodiment of the process according to the invention in which the acidic preparation contains one or more etchable reactive dyes which stain both types of fibers, has the advantage that there are no fission products of disperse dyes which can be difficult to remove from the cellulose fiber. These dyes are preferably applied together with the neutral fixing aid for reactive dyes, whereupon they are fixed in a superheated steam atmosphere.
  • Disperse dyes which can be converted into a water-soluble anionic form with alkali, in particular at a higher temperature, are known.
  • the alkali solubility of these dyes is dependent on functional groups, especially esterified carboxy groups or phenolic or enolic hydroxyl groups or a combination of such groups.
  • these disperse dyes In their water soluble In anionic form, these disperse dyes no longer attach to the polyester fiber and can also be easily removed from the cellulose fiber.
  • the neutral fixing auxiliary for reactive dyestuffs may be added by the appropriate 5 to 100 g p ro liter of padding liquor or per kilogram of printing paste, causes the fixing of the rear Re effetfarbstoffsauf occurs already in the course of Dämpfoperation with superheated steam.
  • these auxiliaries are alkali metal or alkaline earth metal salts of aliphatic or aromatic, preferably low molecular weight, mono- or polycarboxylic acids, in particular alkali metal or alkaline earth metal salts of multiply halogenated low molecular weight aliphatic carboxylic acids and low molecular weight cyclic carbonic acid esters.
  • the alkaline etching paste can be printed on without intermediate drying. In general, however, intermediate drying is recommended.
  • the etching paste contains alkali, preferably in the form of alkali hydroxide or carbonate or a mixture of both, and a reducing agent which is customary in etching and vat printing inks, preferably a stabilized sulfinate, in particular the sodium salt of hydroxymethanesulfinic acid.
  • a suitable dye or a mixture of dyes is added to the alkaline etching paste, which is selected from the range of vat dyes, the alkali-stable dispersion dyes and the combinable dispersion dyes. Combinations of several dyes from different classes are also possible.
  • the alkaline printing paste contains a vat dye
  • treatment with saturated steam at atmospheric pressure follows.
  • the vat dye is incubated so that it can be drawn onto the cellulose portion of the mixed fiber material.
  • vat dyes are very sensitive to temperatures above 100 ° C during the fixing process, but high-temperature fixing is required for the dyes on the polyester fiber portion, it is advisable to add an auxiliary agent that releases water above 100 ° C. This prevents or otherwise at least strongly suppresses the clouding of the color tone.
  • auxiliary agent that releases water above 100 ° C. This prevents or otherwise at least strongly suppresses the clouding of the color tone.
  • auxiliary agents of this type are aqueous dispersions of polymers, for example ethylene polymers, but especially organic dicarboxylic acids which are expediently used in the form of their salts, for example their alkali metal salts. From these aids, 50 to 400 g per kilogram of printing paste are appropriately added.
  • colored reserves are generated with the aid of alkali-stable disperse dyes which are added to the alkaline etching paste.
  • This alkali-stable disperse dye is advantageously used in combination with a vat dye which has the same shade.
  • colored reserve effects are created with the aid of linkable disperse dyes, which in a linked form penetrate the cellulose fiber, where they are firmly anchored in the course of the reoxidation.
  • the fixation of the color depends on the dyes used. As mentioned, saturated steam treatment is required when using vat dyes, which can be omitted if, apart from the reactive dyes, only disperse dyes are used. If saturated steam treatment is carried out, the reactive dye is destroyed by the reducing agent and the alkali-sensitive disperse dye is converted into its water-soluble anionic form in this step.
  • the disperse dyes are expediently fixed in the same unit as a previous saturated steam treatment with superheated steam or hot air in connection with saturated steam. This also promotes reoxidation of the vat dye. If the acidic preparation contains the neutral fixing aid for reactive dyes, the reactive dye is also fixed in this step.
  • the reactive dye is fixed after the fixation of the other dyes by a two-phase steaming process.
  • alkali is applied to the fiber material, preferably in the form of alkali hydroxide, carbonate, bicarbonate, phosphate or silicate or a mixture of such alkalis. It can be applied in any manner, for example by spraying, padding or splashing.
  • the subsequent steaming process is advantageously carried out as short-term steaming in saturated steam, which takes 3 to 20 seconds.
  • the reactive dyes which can be used in the process according to the invention can belong to the various organic dye classes, for example azo, anthraquinone and phthalocyanine dyes, which contain at least one ⁇ -hydroxyethylsulfonic sulfate group, vinylsulfonyl group, monochlorotriazine group, dichlorotriazine group, 2,2,3,3-tetrafluorocyclobutane contain acroylamino group, vinylsulfonylamino group, ß-hydroxyethylsulfonylamino sulfuric acid ester group, ß-phenylsulfonylpropionylamino group or a dichloroquinoxaline group.
  • disperse dyes that can be converted into a water-soluble anionic form with alkali, preferred are those whose cleavage products are easy to eliminate. Dyes which contain one or more carboxylic acid ester groups and nitro-thiazole dyes are preferred.
  • Disperse dyes with an anthrarhinone structure which can be linked, and naphthalene di- and tetracarboxylic acid derivatives and quinophthalone derivatives, which are resistant to alkali and reducing agents, are suitable for the colored etching reserve effects.
  • Vat dyes are in particular indigoid, thioindigoide, anthraquinone or naphthochinoid compounds, which are advantageously used in the commercial dough form.
  • locust bean gum ether thickeners come into consideration. Of this, 50 to 200 g of a 4 to 8% strength are expediently used per liter of liquor added aqueous preparation.
  • Suitable thickeners for the printing pastes are, for example, mixtures of degraded types of rubber and low-viscosity alginates or locust bean gum carboxymethyl ether and starch carboxymethyl ether.
  • the goods are treated with superheated steam for 8 minutes at 180 ° C, briefly rinsed, reoxidized at 50 ° C with 2 g / 1 hydrogen peroxide and 5 ml / 1 acetic acid, rinsed again and finally with 0.5 g / 1 of a 20-fold ethylated nonylphenol washed at 90 ° C, rinsed and dried.
  • a brilliant red print is obtained on a greenish-yellow background with good fastness properties.
  • the goods After printing and drying, the goods are steamed for 10 minutes at 102 ° C in saturated steam and then for 7 minutes at 175 ° C in superheated steam.
  • the further treatment is carried out as in Example 1.
  • the fabric is padded with 50 g / 1 acetic acid in a block bath with a squeezing effect of 70% and then steamed in superheated steam at 175 ° C for 8 minutes.
  • the further treatment is carried out as in Example 1.
  • the result is a deep blue print on a red background with good fastness properties.
  • the fabric After drying, the fabric is printed with a printing ink which, apart from the dye, contains the same constituents as described in Example 1.
  • the printed and dried goods are steamed for 7 minutes at 180 ° C in superheated steam, with a squeezing effect of 70% padded with a liquor of 100 g / l 32.5% sodium hydroxide solution and 150 g / 1 sodium carbonate and 8 seconds in saturated steam Steamed 102 ° C.
  • Completion is as in example 1.
  • the printed and dried fabric is passed through superheated steam at 180 ° C. for 7 minutes and then further treated as in Example 1.
  • the fabric is printed with a printing ink which is composed according to Example 1, but contains no glycerol and 150 g sodium formaldehyde sulfoxylate and correspondingly 160 g water or thickener.
  • a printing ink which is composed according to Example 1, but contains no glycerol and 150 g sodium formaldehyde sulfoxylate and correspondingly 160 g water or thickener.
  • the goods are treated with superheated steam for 8 minutes at 180 ° C, briefly rinsed, reoxidized as usual, washed with 0.5 g / l of a 20-fold ethylated nonylphenol at 90 ° C., rinsed and dried.

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Coloring (AREA)
EP80104279A 1979-07-27 1980-07-21 Procédé pour produire des effets de réserve sur des mélanges de fibres de polyester et de fibres cellulosiques Expired EP0023660B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19792930541 DE2930541A1 (de) 1979-07-27 1979-07-27 Verfahren zur herstellung von reserveeffekten auf mischmaterialien aus polyester- und cellulosefasern
DE2930541 1979-07-27

Publications (3)

Publication Number Publication Date
EP0023660A2 true EP0023660A2 (fr) 1981-02-11
EP0023660A3 EP0023660A3 (en) 1981-05-06
EP0023660B1 EP0023660B1 (fr) 1983-09-28

Family

ID=6076962

Family Applications (1)

Application Number Title Priority Date Filing Date
EP80104279A Expired EP0023660B1 (fr) 1979-07-27 1980-07-21 Procédé pour produire des effets de réserve sur des mélanges de fibres de polyester et de fibres cellulosiques

Country Status (2)

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EP (1) EP0023660B1 (fr)
DE (2) DE2930541A1 (fr)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0051261A1 (fr) * 1980-10-31 1982-05-12 CASSELLA Aktiengesellschaft Procédé pour réaliser des impressions au rongeant-réserve sur des matières textiles
EP0180119A2 (fr) * 1984-10-29 1986-05-07 Hoechst Aktiengesellschaft Procédé de production de réserves blanches et colorées sur des matières fibreuses en polyamide
CN103451800A (zh) * 2013-09-03 2013-12-18 无锡市天然绿色纤维科技有限公司 一种色纺纱线及其加工方法

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4446943A1 (de) * 1994-12-28 1996-07-04 Cassella Ag Verfahren zum Färben von Polyester und polyesterhaltigen Textilmaterialien

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1929231A1 (de) * 1969-06-10 1970-12-17 Hoechst Ag Verfahren zur Herstellung rapportlos gemusterter Druckartil el auf textilen Flaechengebilden
DE2314541A1 (de) * 1973-03-23 1974-10-10 Hoechst Ag Verfahren zur herstellung von aetzeffekten auf faerbungen oder drucken mit dispersionsfarbstoffenauf textilen flaechengebilden aus synthesefasern
DE2326522A1 (de) * 1973-05-24 1974-12-12 Hoechst Ag Verfahren zur herstellung von bunteffekten mit reaktivfarbstoffen unter reaktivfarbstoffen
FR2321009A1 (fr) * 1975-08-13 1977-03-11 Ici Ltd Procede de coloration d'une matiere textile synthetique
DE2836391A1 (de) * 1978-08-19 1980-02-28 Cassella Farbwerke Mainkur Ag Verfahren zum faerben und bedrucken von synthetischem hydrophobem fasermaterial
EP0013378A1 (fr) * 1978-12-27 1980-07-23 CASSELLA Aktiengesellschaft Procédé pour la réalisation d'effets de réserve sur des matières textiles fibreuses mixtes polyester-cellulose
EP0021432A1 (fr) * 1979-07-02 1981-01-07 Hoechst Aktiengesellschaft Procédé d'impression en deux phases pour la préparation d'articles de conversion et de rongeant-réserve

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1929231A1 (de) * 1969-06-10 1970-12-17 Hoechst Ag Verfahren zur Herstellung rapportlos gemusterter Druckartil el auf textilen Flaechengebilden
DE2314541A1 (de) * 1973-03-23 1974-10-10 Hoechst Ag Verfahren zur herstellung von aetzeffekten auf faerbungen oder drucken mit dispersionsfarbstoffenauf textilen flaechengebilden aus synthesefasern
DE2326522A1 (de) * 1973-05-24 1974-12-12 Hoechst Ag Verfahren zur herstellung von bunteffekten mit reaktivfarbstoffen unter reaktivfarbstoffen
FR2321009A1 (fr) * 1975-08-13 1977-03-11 Ici Ltd Procede de coloration d'une matiere textile synthetique
GB1543724A (en) * 1975-08-13 1979-04-04 Ici Ltd Process for the production of discharge printing effects on synthetic textile materials
DE2836391A1 (de) * 1978-08-19 1980-02-28 Cassella Farbwerke Mainkur Ag Verfahren zum faerben und bedrucken von synthetischem hydrophobem fasermaterial
GB2028383A (en) * 1978-08-19 1980-03-05 Cassella Ag Process for dyeing and printing synthetic hydrophobic fibre material
EP0013378A1 (fr) * 1978-12-27 1980-07-23 CASSELLA Aktiengesellschaft Procédé pour la réalisation d'effets de réserve sur des matières textiles fibreuses mixtes polyester-cellulose
EP0021432A1 (fr) * 1979-07-02 1981-01-07 Hoechst Aktiengesellschaft Procédé d'impression en deux phases pour la préparation d'articles de conversion et de rongeant-réserve

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
RESEARCH DISCLOSURE, Band 174, Nr. 1, 10. Oktober 1978, Seiten 19,20, Nr. 17405, Havant, Hampshire, GB * Ganz * *

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0051261A1 (fr) * 1980-10-31 1982-05-12 CASSELLA Aktiengesellschaft Procédé pour réaliser des impressions au rongeant-réserve sur des matières textiles
EP0180119A2 (fr) * 1984-10-29 1986-05-07 Hoechst Aktiengesellschaft Procédé de production de réserves blanches et colorées sur des matières fibreuses en polyamide
EP0180119A3 (en) * 1984-10-29 1987-08-26 Hoechst Aktiengesellschaft Process for producing white and coloured resists on polyamide fibrous materials
CN103451800A (zh) * 2013-09-03 2013-12-18 无锡市天然绿色纤维科技有限公司 一种色纺纱线及其加工方法
CN103451800B (zh) * 2013-09-03 2016-02-03 无锡市天然绿色纤维科技有限公司 一种色纺纱线及其加工方法

Also Published As

Publication number Publication date
DE3065045D1 (en) 1983-11-03
EP0023660A3 (en) 1981-05-06
EP0023660B1 (fr) 1983-09-28
DE2930541A1 (de) 1981-02-12

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