EP1664420A2 - Process for printing or dyeing cellulose/polyester mixed fibres - Google Patents

Process for printing or dyeing cellulose/polyester mixed fibres

Info

Publication number
EP1664420A2
EP1664420A2 EP04766635A EP04766635A EP1664420A2 EP 1664420 A2 EP1664420 A2 EP 1664420A2 EP 04766635 A EP04766635 A EP 04766635A EP 04766635 A EP04766635 A EP 04766635A EP 1664420 A2 EP1664420 A2 EP 1664420A2
Authority
EP
European Patent Office
Prior art keywords
hydrogen
denotes
formula
process according
alkyl
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.)
Withdrawn
Application number
EP04766635A
Other languages
German (de)
French (fr)
Inventor
Véronique Hall-Goulle
Athanassios Tzikas
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.)
Huntsman Advanced Materials Switzerland GmbH
Original Assignee
Ciba Spezialitaetenchemie Holding AG
Ciba SC Holding 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 Ciba Spezialitaetenchemie Holding AG, Ciba SC Holding AG filed Critical Ciba Spezialitaetenchemie Holding AG
Priority to EP04766635A priority Critical patent/EP1664420A2/en
Publication of EP1664420A2 publication Critical patent/EP1664420A2/en
Withdrawn legal-status Critical Current

Links

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
    • D06P3/34—Material containing ester groups
    • D06P3/36—Material containing ester groups using dispersed dyestuffs
    • 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
    • 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
    • D06P1/16—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 dispersed, e.g. acetate, dyestuffs
    • 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
    • D06P1/44—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 insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/60—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 insoluble pigments or auxiliary substances, e.g. binders using compositions containing polyethers
    • D06P1/613—Polyethers without nitrogen
    • 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
    • D06P1/44—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 insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/60—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 insoluble pigments or auxiliary substances, e.g. binders using compositions containing polyethers
    • D06P1/613—Polyethers without nitrogen
    • D06P1/6138—Polymerisation products of glycols, e.g. Carbowax, Pluronics
    • 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
    • D06P1/90—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 dyes dissolved in organic solvents or aqueous emulsions thereof
    • D06P1/908—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 dyes dissolved in organic solvents or aqueous emulsions thereof using specified 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
    • 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
    • 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
    • D06P3/8228—Textiles which contain different kinds of fibres fibres of different chemical nature mixtures of fibres containing hydroxyl and ester groups using one kind of dye
    • D06P3/8233—Textiles which contain different kinds of fibres fibres of different chemical nature mixtures of fibres containing hydroxyl and ester groups using one kind of dye using dispersed dyes

Definitions

  • the invention relates to a process for printing or dyeing water swellable cellulose fibres or cellulose/polyester mixed fibres with specific disperse dyes.
  • DE 1 811 796 describes a process for dyeing cellulose fibres or blends of cellulose fibres and synthetic fibres with a single disperse dye which process comprises contacting said cellulosic material with water in sufficient amount to swell the cellulose, a solution or dispersion of the dye and a high-boiling water-soluble solvent in an amount sufficient to maintain swelling of the cellulose if water is removed.
  • the present invention relates to a process for printing or dyeing cellulose fibres or cellulose/polyester mixed fibres characterised in that the fibres are treated in any sequence with water, a water-soluble organic solvent having a boiling point >150 °C and a disperse dye selected from the compounds of formulae (1) to (10)
  • Ri and R 2 are each independently of the other C ⁇ -C 8 -alkyl, -(CH 2 ) n -O-(CH2) m R 5 , wherein R 5 denotes hydrogen or C ⁇ -C 8 -alkyl, n is a number from 2 to 6 and m is a number from 0 to 6, Cs-C ⁇ aryl, which is unsubstituted or substituted with one or more hydroxy groups, C C 8 alkyl groups, CrC alkoxy groups or halogen atoms or C ⁇ -Csoaralkyl, which is unsubstituted or substituted with one or more hydroxy groups, C ⁇ -C alkyl groups, Cr
  • R 3 and R are each independently of the other chlorine, bromine, cyano, methyl or trifluoromethyl,
  • X is a radical of formula (1a), (1 b), (1c) or (1d)
  • R 6 and R 7 independently of the other represent hydrogen, chlorine, bromine or cyano
  • R 8 denotes CrC 8 -alkyl or -(CH 2 ) n -O-(CH 2 ) m R 5 ⁇ wherein R denotes hydrogen or C C 8 -alkyI, n is a number from 2 to 6 and m is a number from 0 to 6,
  • R 9 is hydrogen, fluorine, chlorine, bromine, cyano, methyl, trifluoromethyl or-SO 2 CH 3 and
  • R 10 represents hydrogen, hydroxy or amino
  • Rn denotes a radical of formula (2a), (2b), (2c) or (2d) wherein R 17 is hydrogen, chlorine , bromine, methyl or methoxy,
  • R 18 is hydrogen, phenylamino, benzamido or CrC ⁇ 2 acyIamido, one of the radicals R ⁇ 2 , R 13 and R M denotes a radical of formula (2a), (2b), (2c) or (2d) as defined above and the others are hydrogen, and
  • R 15 and R ⁇ 6 are each independently of the other hydrogen, bromine or chlorine;
  • R 19 denotes C C 8 alkyl or -(CH 2 ) n -O-(CH 2 ) m -OR 2 o
  • R 20 is hydrogen, methyl or ethyl
  • n denotes a number from 2 to 6
  • m denotes a number from 0 to 6;
  • R 2 ⁇ is C C 8 alkyl, Cs-C 2 aryl, which is unsubstituted or substituted with one or more hydroxy groups, C C 8 alkyl groups, d-C 4 alkoxy groups or halogen atoms or C 6 -C 3 oaralkyl, which is unsubstituted or substituted with one or more hydroxy groups, C C alkyl groups,
  • R 22 and R 23 are each independently of the other hydrogen, bromine or chlorine;
  • R 24 denotes chlorine, bromine, cyano or-CONH 2 ,
  • R 25 is CrC 20 alkyl or -(CH 2 ) n -0-(CH 2 ) m R 5 , wherein R 5 denotes hydrogen or d-C ⁇ -alkyl, n is a number from 2 to 6 and m is a number from 0 to 6,
  • D is a radical of formula (1c) as defined above or a radical of formula (6a)
  • R 9 , R 10 and R 25 are as defined above;
  • R 26 denotes CrC 12 alkoxy
  • Me denotes Ni, Zn, Pd or preferably Cu
  • R 27 is hydrogen, d-C ⁇ alkoxy or -SO 2 -NH-R 25 and R 2 5 is as defined above; wherein R 28 and R 29 are each independently of the other a radical of formula (2b) or (2d) as defined above;
  • R 8 and R17 are as defined above.
  • the compounds of formulae (1) to (10) are known and either commercially available or can be prepared according to known processes.
  • Preferred compounds of formula (1) are those wherein R 3 is cyano and R 4 is methyl.
  • a compound of formula (1) is used as disperse dye, wherein R 3 is cyano, R 4 is methyl and X is a radical of formula (1a), (1b) or (1d).
  • Particularly preferred disperse dyes are the compounds of formula (1 ), wherein R 3 is cyano, R 4 is methyl and X is a radical of formula (1d).
  • Particularly preferred disperse dyes are the compounds of formulae (101), (102), (108), (109), (110), (115), (116), (118), (119), (120), (124), (133), (141), (143), (144), (152) and (154).
  • the most preferred disperse dyes are the compounds of formula (101) and (102)
  • the organic solvent used in the process according to the invention should be water-soluble and have a high dissolving capacity for the disperse dyes of formulae (1) to (10) at the fixation temperature.
  • Water-soluble in this context means solubility in water of at least 2.5 % by weight at 25 °C.
  • Suitable solvents of this type are glycols and their derivatives, in particular the ethers and esters.
  • the preferred organic solvents that can be applied in the process according to the invention are polyethylene glycol, polypropylene glycol or an ether or ester derivative of polyethylene glycol or polypropylene glycol.
  • Polyethylene glycol having a molecular weight of 100 to 600 is particularly preferred.
  • water, dye and solvent can be applied to the substrate in any sequence.
  • the preferred method for dyeing fabrics composed of cellulosic fibres or mixtures of cellulosic and synthetic fibres is to impregnate the fabric with a mixture of one or more dyes, water and solvent in a conventional dye pad bath followed by squeezing to remove excess dye liquor, or to print with a solvent-containing printing paste, and subsequently heating to evaporate sufficient water to effect dissolution of the dye, at which time the fabric is dyed.
  • water is evaporated, but in an insufficient amount to effect dissolution of the dye, after which pressure and heat are applied to effect dissolution without further evaporation of water.
  • Dye pastes can be prepared by conventional techniques such as by milling the dye in the presence of a dispersing agent or surfactant.
  • a dyebath can be prepared by diluting the dye paste with water or with aqueous solvent. Addition of a solvent to the dye paste before addition of water may cause dye separation and usually is avoided. It will be understood by those skilled in the art that conventional additives other than a dye solvent and a dispersing agent can be present in dye baths and printing pastes.
  • Further components which may be present in the printing pastes or dye baths are e.g. natural or synthetic thickeners, pigments, acids, bases and/or salts to adjust the pH to the desired value, anionic, nonionic or cationic surfactants, antifoaming and antifrosting agents, dispersing agents, fixing agents, polyhydroxy compounds, reaction products of hydroxyl compounds and isocyanates, polyesters prepared by reaction of terephthalic acid and one or more polyethylene glycols. These components are commonly used or recommended for textile printing or finishing.
  • the three components are preferably contemporaneously applied to the fibre.
  • the relative amounts of water, solvent and dye that can be applied in the printing pastes and dye baths are known to the skilled artisan.
  • the printing paste which can be applied in the process according to the invention preferably contains 50 to 95 %, more preferably 60 to 90 % and in particular 70 to 85 by weight of water, based on the total weight of the printing paste.
  • the amount of organic solvent is preferably 1 to 20 %, more preferably 2 to 15 % and in particular 5 to 10 by weight of, based on the total weight of the printing paste.
  • the amount of dye dispersion is preferably 1 to 15 %, more preferably 2 to 10 % and in particular 3 to 8 by weight of, based on the total weight of the printing paste.
  • the temperature at which dyeing or printing is effected by the instant process depends on the solubility of the dye in the dye solvent or aqueous dye solvent.
  • the fibres are heated in a liquor at 125 °C to 225 °C, said liquor containing as liquid ingredients 10 to 95 % by weight of water and 5 to 90 % by weight of organic solvent.
  • the cellulosic materials which can be dyed by the process of this invention include all forms of cellulose which increase in size and flexibility upon exposure to water. Suitable materials include natural fibres and purified wood pulps as well as reconstituted cellulose in fiber and film form.
  • the invention is particularly useful for dyeing cotton/polyester mixed fibres.
  • Each dye is dispersed according to the following formulation: • 29,2% dye • 7.3% 1,2-propylenglykol (solvent) • 3.7% Lutensol AT25 (dispersant) • 0.8% Geropon T77 (wetting agent) • 0.1 % Surfinol DF58 (antifoam agent) • 0.4% Proxel GXL (antimicrobial) • 58.5% deionised water
  • Zirconium beads (diameter 0.6 to 1 mm) are then added to the above-obtained dispersion in a glass bottle tightly closed. The bottle is then placed in a Scandex apparatus and thereby agitated for 4 hours.
  • the thus obtained fine dispersion is then filtered on a conventional Buchner funnel to provide the final dye dispersion.
  • Printing paste A typical run consists in the preparation of a mother paste, to which a quantity of the dye dispersion and water will be subsequently added.
  • the amount of added deionised water can vary as a function of the viscosity of the dye dispersion and/or of the printing paste.
  • the printing paste is applied in a classical way on the textile (CO or PES/CO) through a screen. After drying at 90°C, the textile is thermofixed at 220°C for 1 minute.

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Coloring (AREA)

Abstract

The invention relates to a process for printing or dyeing cellulose fibres or cellulose/polyester mixed fibres characterised in that the fibres are treated in any sequence with water, a watersoluble organic solvent having a boiling point >150 °C and a specific disperse dye.

Description

Process for Printing or Dyeing Cellulose or Cellulose/Polyester Mixed Fibres
The invention relates to a process for printing or dyeing water swellable cellulose fibres or cellulose/polyester mixed fibres with specific disperse dyes.
Many attempts have been made to develop efficient processes for printing or dyeing polyester-cotton blends.
Two fundamentally different approaches were taken:
Processes using one class of dye only and processes using mixtures of two classes of dyes. Usually reactive dyes or vat dyes are combined with disperse dyes. However, the use of such dye mixtures is associated with several drawbacks and it is hardly possible to obtain the same colour and depth on the two fibres by this method.
DE 1 811 796 describes a process for dyeing cellulose fibres or blends of cellulose fibres and synthetic fibres with a single disperse dye which process comprises contacting said cellulosic material with water in sufficient amount to swell the cellulose, a solution or dispersion of the dye and a high-boiling water-soluble solvent in an amount sufficient to maintain swelling of the cellulose if water is removed.
In J. Soc. Dyers Colour., 96, 347-354 (1980) specific disperse dyes (Cellestren®, supplied by BASF) in combination with Glyezin® CD, a polyalkylene oxide derivative, are recommended for application in the printing process described in DE 1 811 796. The prints on polyester- cotton blends obtained by this process are described as exhibiting brilliant colours with the same depth of colour on both fibres.
However, the Cellestren/Glyezin system does not meet the top requirements with respect to light fastness and wash fastness.
It has now been found that the application of some specific disperse dyes in the process disclosed in DE 1 811 796 yields prints and dyeings on polyester-cotton blends having extraordinarily good light fastness and wash fastness.
The present invention relates to a process for printing or dyeing cellulose fibres or cellulose/polyester mixed fibres characterised in that the fibres are treated in any sequence with water, a water-soluble organic solvent having a boiling point >150 °C and a disperse dye selected from the compounds of formulae (1) to (10)
wherein Ri and R2 are each independently of the other Cι-C8-alkyl, -(CH2)n-O-(CH2)mR5, wherein R5 denotes hydrogen or Cι-C8-alkyl, n is a number from 2 to 6 and m is a number from 0 to 6, Cs-C^aryl, which is unsubstituted or substituted with one or more hydroxy groups, C C8alkyl groups, CrC alkoxy groups or halogen atoms or Cβ-Csoaralkyl, which is unsubstituted or substituted with one or more hydroxy groups, Cι-C alkyl groups, Cr
C4alkoxy groups or halogen atoms,
R3 and R are each independently of the other chlorine, bromine, cyano, methyl or trifluoromethyl,
X is a radical of formula (1a), (1 b), (1c) or (1d)
wherein R6 and R7 independently of the other represent hydrogen, chlorine, bromine or cyano,
R8 denotes CrC8-alkyl or -(CH2)n-O-(CH2)mR5ι wherein R denotes hydrogen or C C8-alkyI, n is a number from 2 to 6 and m is a number from 0 to 6,
R9 is hydrogen, fluorine, chlorine, bromine, cyano, methyl, trifluoromethyl or-SO2CH3 and
R10 represents hydrogen, hydroxy or amino;
wherein Rn denotes a radical of formula (2a), (2b), (2c) or (2d) wherein R17 is hydrogen, chlorine , bromine, methyl or methoxy,
R18 is hydrogen, phenylamino, benzamido or CrCι2acyIamido, one of the radicals Rι2, R13 and RM denotes a radical of formula (2a), (2b), (2c) or (2d) as defined above and the others are hydrogen, and
R15 and Rι6 are each independently of the other hydrogen, bromine or chlorine;
wherein R19 denotes C C8alkyl or -(CH2)n-O-(CH2)m-OR2o, and R20 is hydrogen, methyl or ethyl, n denotes a number from 2 to 6 and m denotes a number from 0 to 6;
wherein R2ι is C C8alkyl, Cs-C2 aryl, which is unsubstituted or substituted with one or more hydroxy groups, C C8alkyl groups, d-C4alkoxy groups or halogen atoms or C6-C3oaralkyl, which is unsubstituted or substituted with one or more hydroxy groups, C C alkyl groups,
CrC alkoxy groups or halogen atoms;
wherein R22 and R23 are each independently of the other hydrogen, bromine or chlorine;
wherein R24 denotes chlorine, bromine, cyano or-CONH2,
R25 is CrC20alkyl or -(CH2)n-0-(CH2)mR5, wherein R5 denotes hydrogen or d-Cβ-alkyl, n is a number from 2 to 6 and m is a number from 0 to 6,
D is a radical of formula (1c) as defined above or a radical of formula (6a)
wherein R9, R10 and R25 are as defined above;
wherein R26 denotes CrC12alkoxy;
wherein Me denotes Ni, Zn, Pd or preferably Cu,
R27 is hydrogen, d-C^alkoxy or -SO2-NH-R25 and R25 is as defined above; wherein R28 and R29 are each independently of the other a radical of formula (2b) or (2d) as defined above;
wherein R8 and R17 are as defined above.
The compounds of formulae (1) to (10) are known and either commercially available or can be prepared according to known processes.
Preferred compounds of formula (1) are those wherein R3 is cyano and R4 is methyl.
In a preferred embodiment of the invention a compound of formula (1) is used as disperse dye, wherein R3 is cyano, R4 is methyl and X is a radical of formula (1a), (1b) or (1d).
Particularly preferred disperse dyes are the compounds of formula (1 ), wherein R3 is cyano, R4 is methyl and X is a radical of formula (1d).
Further preferred disperse dyes are the following compounds:
Particularly preferred disperse dyes are the compounds of formulae (101), (102), (108), (109), (110), (115), (116), (118), (119), (120), (124), (133), (141), (143), (144), (152) and (154).
The most preferred disperse dyes are the compounds of formula (101) and (102)
All the embodiments described in DE 1 811 796, hereby incorporated by reference, can basically be performed by using the disperse dyes of formula (1) to (10).
The organic solvent used in the process according to the invention should be water-soluble and have a high dissolving capacity for the disperse dyes of formulae (1) to (10) at the fixation temperature. Water-soluble in this context means solubility in water of at least 2.5 % by weight at 25 °C.
Suitable solvents of this type are glycols and their derivatives, in particular the ethers and esters. The preferred organic solvents that can be applied in the process according to the invention are polyethylene glycol, polypropylene glycol or an ether or ester derivative of polyethylene glycol or polypropylene glycol.
Polyethylene glycol having a molecular weight of 100 to 600 is particularly preferred.
In dyeing cellulosic materials by the process of the invention, water, dye and solvent can be applied to the substrate in any sequence. The preferred method for dyeing fabrics composed of cellulosic fibres or mixtures of cellulosic and synthetic fibres is to impregnate the fabric with a mixture of one or more dyes, water and solvent in a conventional dye pad bath followed by squeezing to remove excess dye liquor, or to print with a solvent-containing printing paste, and subsequently heating to evaporate sufficient water to effect dissolution of the dye, at which time the fabric is dyed. Alternatively, water is evaporated, but in an insufficient amount to effect dissolution of the dye, after which pressure and heat are applied to effect dissolution without further evaporation of water. Dye pastes can be prepared by conventional techniques such as by milling the dye in the presence of a dispersing agent or surfactant. A dyebath can be prepared by diluting the dye paste with water or with aqueous solvent. Addition of a solvent to the dye paste before addition of water may cause dye separation and usually is avoided. It will be understood by those skilled in the art that conventional additives other than a dye solvent and a dispersing agent can be present in dye baths and printing pastes.
Further components which may be present in the printing pastes or dye baths are e.g. natural or synthetic thickeners, pigments, acids, bases and/or salts to adjust the pH to the desired value, anionic, nonionic or cationic surfactants, antifoaming and antifrosting agents, dispersing agents, fixing agents, polyhydroxy compounds, reaction products of hydroxyl compounds and isocyanates, polyesters prepared by reaction of terephthalic acid and one or more polyethylene glycols. These components are commonly used or recommended for textile printing or finishing.
Although it is possible to treat the fibres in any sequence with water, solvent and dye, the three components are preferably contemporaneously applied to the fibre. The relative amounts of water, solvent and dye that can be applied in the printing pastes and dye baths are known to the skilled artisan.
The printing paste which can be applied in the process according to the invention preferably contains 50 to 95 %, more preferably 60 to 90 % and in particular 70 to 85 by weight of water, based on the total weight of the printing paste.
The amount of organic solvent is preferably 1 to 20 %, more preferably 2 to 15 % and in particular 5 to 10 by weight of, based on the total weight of the printing paste.
The amount of dye dispersion is preferably 1 to 15 %, more preferably 2 to 10 % and in particular 3 to 8 by weight of, based on the total weight of the printing paste.
The temperature at which dyeing or printing is effected by the instant process depends on the solubility of the dye in the dye solvent or aqueous dye solvent.
Preferably, the fibres are heated in a liquor at 125 °C to 225 °C, said liquor containing as liquid ingredients 10 to 95 % by weight of water and 5 to 90 % by weight of organic solvent.
The cellulosic materials which can be dyed by the process of this invention include all forms of cellulose which increase in size and flexibility upon exposure to water. Suitable materials include natural fibres and purified wood pulps as well as reconstituted cellulose in fiber and film form.
The invention is particularly useful for dyeing cotton/polyester mixed fibres.
The following non-limitative Examples illustrate the invention in more detail. Application Examples:
1. Dispersion
Each dye is dispersed according to the following formulation: • 29,2% dye • 7.3% 1,2-propylenglykol (solvent) • 3.7% Lutensol AT25 (dispersant) • 0.8% Geropon T77 (wetting agent) • 0.1 % Surfinol DF58 (antifoam agent) • 0.4% Proxel GXL (antimicrobial) • 58.5% deionised water
Zirconium beads (diameter 0.6 to 1 mm) are then added to the above-obtained dispersion in a glass bottle tightly closed. The bottle is then placed in a Scandex apparatus and thereby agitated for 4 hours.
The thus obtained fine dispersion is then filtered on a conventional Buchner funnel to provide the final dye dispersion.
2. Printing paste A typical run consists in the preparation of a mother paste, to which a quantity of the dye dispersion and water will be subsequently added.
Mother paste: • 84.2% deionised water • 0.8% NH4OH (28%) • 0.4% Alcoprint PA-NS • 9.9% PEG400 • 2.3% Alcoprint PSC • 2.4% Alcoprint PTP
Printing paste • 33.3% deionised water • 60.1 % mother paste • 6.6% dye dispersion The amount of added deionised water can vary as a function of the viscosity of the dye dispersion and/or of the printing paste.
3. Printing
The printing paste is applied in a classical way on the textile (CO or PES/CO) through a screen. After drying at 90°C, the textile is thermofixed at 220°C for 1 minute.
After a brief cold rinse, a 30 minutes wash at 80°C is performed in a bath containing: • 2g/L carbonate • 1g/L Calgon • 1g/L UItravon JU
4. Tests All thus obtained printed fabrics exhibit a very good light fastness, wash fastness and wet rubbing fastness.

Claims

Claims
1. A process for printing or dyeing cellulose fibres or cellulose/polyester mixed fibres characterised in that the fibres are treated in any sequence with water, a water-soluble organic solvent having a boiling point >150 °C and a disperse dye selected from the compounds of formulae (1) to (10)
wherein R^ and R2 are each independently of the other Cι-C8-alkyl, -(CH2)n-0-(CH2)mR5, wherein R5 denotes hydrogen or CrC8-alkyl, n is a number from 2 to 6 and m is a number from 0 to 6, C5-C24aryl, which is unsubstituted or substituted with one or more hydroxy groups, C C8alkyl groups, C C4alkoxy groups or halogen atoms or Ce-Csoaralkyl, which is unsubstituted or substituted with one or more hydroxy groups, C C4alkyl groups, C C alkoxy groups or halogen atoms,
R3 and R4 are each independently of the other chlorine, bromine, cyano, methyl or trifluoromethyl,
X is a radical of formula (1a), (1b), (1c) or (1d)
wherein R6 and R7 independently of the other represent hydrogen, chlorine, bromine or cyano,
R8 denotes CrC8-alkyl or -(CH2)n-O-(CH2)mR5, wherein R5 denotes hydrogen or C C8-alkyl, n is a number from 2 to 6 and m is a number from 0 to 6, R9 is hydrogen, fluorine, chlorine, bromine, cyano, methyl, trifluoromethyl or-SO2CH3 and
Rio represents hydrogen, hydroxy or amino; wherein Rn denotes a radical of formula (2a), (2b), (2c) or (2d)
wherein R17 is hydrogen, chlorine , bromine, methyl or methoxy, Rι8 is hydrogen, phenylamino, benzamido or C C12acylamido, one of the radicals Rι2, R13 and RM denotes a radical of formula (2a), (2b), (2c) or (2d) as defined above and the others are hydrogen, and
R15 and Rι6 are each independently of the other hydrogen, bromine or chlorine;
wherein R19 denotes Cι-C8alkyl or -(CH2)n-O-(CH2)m-OR2o, and R2o is hydrogen, methyl or ethyl, n denotes a number from 2 to 6 and m denotes a number from 0 to 6;
wherein R2ι is CrC8alkyl, C5-C2 aryl, which is unsubstituted or substituted with one or more hydroxy groups, C C8alkyl groups, C C4alkoxy groups or halogen atoms or C6-C3oaralkyl, which is unsubstituted or substituted with one or more hydroxy groups, C C4alkyl groups, d-C alkoxy groups or halogen atoms;
wherein R22 and R23 are each independently of the other hydrogen, bromine or chlorine;
wherein R2 denotes chlorine, bromine, cyano or -CONH2,
R25 is Ci-C2oalkyl or -(CH2)n-0-(CH2)mR5, wherein R5 denotes hydrogen or Cι-C8-alkyl, n is a number from 2 to 6 and m is a number from 0 to 6,
D is a radical of formula (1c) as defined above or a radical of formula (6a)
wherein R9, R10 and R25 are as defined above;
wherein R26 denotes C C12alkoxy;
wherein Me denotes Cu, Ni, Zn or Pd,
R27 is hydrogen, d-C^alkoxy or -SO2-NH-R25 and R25 is as defined above;
wherein R28 and R29 are each independently of the other a radical of formula (2b) or (2d) as defined above;
wherein R8 and R17 are as defined above.
2. A process according to claim 1, characterised in that a compound of formula (1) is used as disperse dye, wherein R3 is cyano and R4 is methyl.
3. A process according to claim 2, characterised in that a compound of formula (1) is used as disperse dye, wherein X is a radical of formula (1a), (1b) or (1d).
4. A process according to claim 3, characterised in that the disperse dye is a compound of formula (101) or (102)
5. A process according to claim 1, characterised in that the organic solvent is polyethylene glycol, polypropylene glycol or an ether or ester derivative of polyethylene glycol or polypropylene glycol.
6. A process according to claim 5, characterised in that the organic solvent is polyethylene glycol having a molecular weight of 100 to 600.
7. A process according to claim 1 , characterised in that water, organic solvent and disperse dye are contemporaneously applied to the fibre.
8. A printing process according to claim 1, characterised in that the printing paste contains 50 to 95 % by weight of water, based on the total weight of the printing paste.
9. A printing process according to claim 1, characterised in that the printing paste contains 1 to 20 % by weight of organic solvent, based on the total weight of the printing paste.
10. A printing process according to claim 1, characterised in that the printing paste contains 1 to 15 % by weight of a dye dispersion, based on the total weight of the printing paste.
11. A dyeing process according to claim 1 , characterised in that the fibres are heated in a liquor at 125 °C to 225 °C, said liquor containing as liquid ingredients 10 to 95 % by weight of water and 5 to 90 % by weight of organic solvent.
12. A process according to claim 1, characterised in that the fibres are cotton/polyester mixed fibres.
EP04766635A 2003-09-08 2004-08-30 Process for printing or dyeing cellulose/polyester mixed fibres Withdrawn EP1664420A2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP04766635A EP1664420A2 (en) 2003-09-08 2004-08-30 Process for printing or dyeing cellulose/polyester mixed fibres

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP03405656 2003-09-08
PCT/EP2004/051952 WO2005024123A2 (en) 2003-09-08 2004-08-30 Process for printing or dyeing cellulose/polyester mixed fibres
EP04766635A EP1664420A2 (en) 2003-09-08 2004-08-30 Process for printing or dyeing cellulose/polyester mixed fibres

Publications (1)

Publication Number Publication Date
EP1664420A2 true EP1664420A2 (en) 2006-06-07

Family

ID=34259308

Family Applications (1)

Application Number Title Priority Date Filing Date
EP04766635A Withdrawn EP1664420A2 (en) 2003-09-08 2004-08-30 Process for printing or dyeing cellulose/polyester mixed fibres

Country Status (6)

Country Link
US (1) US20070000076A1 (en)
EP (1) EP1664420A2 (en)
KR (1) KR20060090805A (en)
CN (1) CN1846028A (en)
TW (1) TW200523428A (en)
WO (1) WO2005024123A2 (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007017430A1 (en) * 2005-08-11 2007-02-15 Huntsman Advanced Materials (Switzerland) Gmbh Infrared ray-absorbing fibers
US8399161B2 (en) 2007-02-23 2013-03-19 Basf Se Transparent colourants and colourant compositions, and their use
KR101231050B1 (en) * 2010-11-29 2013-02-07 주식회사에스케이니트 Dyeing method of rayon-polyester union cloth
KR101231051B1 (en) * 2010-11-29 2013-02-07 주식회사에스케이니트 Textile printing method of rayon-polyester union cloth
TWI707002B (en) * 2016-05-25 2020-10-11 瑞士商杭斯曼高級材料公司 Disperse azo dyes, a process for the preparation thereof and the use thereof
PT3574055T (en) 2017-01-27 2023-04-13 Huntsman Textile Effects Switzerland Gmbh Method for printing textile fibre materials in accordance with the ink-jet printing process
WO2018177652A1 (en) 2017-03-29 2018-10-04 Huntsman Advanced Materials (Switzerland) Gmbh Process for printing cellulose containing textile fibre material
ES3001083T3 (en) * 2017-04-07 2025-03-04 Archroma Switzerland Gmbh Mixtures of dyes
CN111527257B (en) 2017-06-22 2022-01-28 Hbi品牌服饰企业有限公司 Fabric treatment composition and method

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1811796C3 (en) * 1968-11-25 1974-01-03 E.I. Du Pont De Nemours And Co., Wilmington, Del. (V.St.A.) Process for dyeing cellulose fibers or mixtures thereof with synthetic fibers
US3706525A (en) * 1971-03-08 1972-12-19 Du Pont Water swollen cellulose dyeing with high molecular weight disperse dye in a glycol ether solution
US3744967A (en) * 1971-03-22 1973-07-10 Du Pont Process for dyeing napped fabrics of water swellable cellulose fibers
DE2528743C2 (en) * 1975-06-27 1982-06-09 Basf Ag, 6700 Ludwigshafen Process for dyeing and printing cellulose fibers or mixtures of cellulose fibers with synthetic fibers
AT373930B (en) * 1975-10-29 1984-03-12 Basf Ag DYE PREPARATIONS FOR DYEING AND PRINTING CELLULOSE AND CELLULOSE-CONTAINING TEXTILE MATERIAL
DE4432833A1 (en) * 1994-09-15 1996-03-21 Basf Ag Process for coloring melamine-formaldehyde condensation products

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2005024123A2 *

Also Published As

Publication number Publication date
WO2005024123A3 (en) 2005-06-02
WO2005024123A2 (en) 2005-03-17
US20070000076A1 (en) 2007-01-04
KR20060090805A (en) 2006-08-16
TW200523428A (en) 2005-07-16
CN1846028A (en) 2006-10-11

Similar Documents

Publication Publication Date Title
EP0775776B1 (en) Process for di- or trichromic dyeing or printing
JPH11158402A (en) Disperse dye composition and method for coloring hydrophobic material using the same
WO2005024123A2 (en) Process for printing or dyeing cellulose/polyester mixed fibres
US3288551A (en) Process for the coloring of fiber blends of polyester and native or regenerated cellulose
US3990846A (en) Process for the continuous dyeing and printing of piece goods
JPH09176509A (en) High light resistance coloring composition and method for coloring hydrophobic material using the same
KR920000745B1 (en) Composition of monoazo dyestaffs
CN111117290B (en) Disperse red dye composition and dye product
US5324330A (en) Dye mixtures and the use thereof
EP2958962B1 (en) Mixtures of reactive dyes and their use in a method of di- or trichromatic dyeing or printing
KR20040012521A (en) Non-azo disperse dye mixtures
EP0742270A2 (en) Mixtures of phthalocyanine reactive dyes
JPH01289870A (en) Mixture of monoazo dyes
US4560387A (en) Aqueous formulations for dyeing and printing blended fabrics
US3835154A (en) Blue disperse 1,4-diaminoanthraquinone-2,3-dicarboximide dyes
JP3170917B2 (en) Benzodifuranone-containing composition and method for coloring hydrophobic material using the same
JPH06240586A (en) Method for dyeing of natural or synthetic polyamide fiber material with dye mixture
JPH04226571A (en) Mixture of monoazo dye
US4235596A (en) Process for the pad-dyeing and printing of textile material made from mixed fibres of cellulose and polyester
US4193763A (en) Dyeing and printing of water-swellable cellulose material and blends thereof with synthetic fibres, by means of disazo dyes derived from amino-pyrazole
DE3320430C2 (en)
CN109796785A (en) A kind of reactive blue is to black dye composition and dye preparations and its application
TWI835843B (en) New pyridine- and pyrimidine-substituted triazine uv absorbers
KR100251605B1 (en) Method for preparing monoazo dye mixtures and dyeing and printing methods using the same
JPH05263004A (en) Process for dyeing or printing hydroxyl group-containing fiber material

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20060119

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LI LU MC NL PL PT RO SE SI SK TR

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: HUNTSMAN ADVANCED MATERIALS (SWITZERLAND) GMBH

DAX Request for extension of the european patent (deleted)
17Q First examination report despatched

Effective date: 20090807

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20091218