Classifications

• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
  • D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
  • D06P1/44—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
  • D06P1/62—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 low-molecular-weight organic compounds with sulfate, sulfonate, sulfenic or sulfinic groups
  • D06P1/621—Compounds without nitrogen
  • D06P1/622—Sulfonic acids or their salts
• • 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
  • D06P1/64—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 low-molecular-weight organic compounds without sulfate or sulfonate groups
  • D06P1/651—Compounds without nitrogen
  • D06P1/65106—Oxygen-containing compounds
  • D06P1/65131—Compounds containing ether or acetal 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
  • 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
  • D06P1/64—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 low-molecular-weight organic compounds without sulfate or sulfonate groups
  • D06P1/651—Compounds without nitrogen
  • D06P1/6515—Hydrocarbons
  • D06P1/65162—Hydrocarbons without halogen
• • 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
  • D06P3/52—Polyesters
  • D06P3/54—Polyesters using dispersed dyestuffs

Definitions

• ABSTRACT Carrier composition comprising a mixture of methylnapthalene and diphenylene oxide and the use thereof in the dyeing and printing of synthetic fibers.
• Carriers are understood to be chemical compositions which are added to the dye bath in a finely dispersed or emulsified form or are precipitated in the dye bath in a finely dispersed form and which promote the penetration of the dyestuff into the fiber, whereby a considerable increase in the color depth of the dyeings or prints is achieved.
• Methylnaphthalene is one of these.
• the use of methylnaphthalene as the carrier offers a disadvantage because a residue thereof remains on the dyed fiber and impairs fastness to light of the dyed and printed materials.
• the methylnaphthalene residue retained by the fibers may be removed as a practical matter only by a special heat treatment, temperatures of at least 150C. and processing times of at least 3 minutes being required.
• the required additional heat treatment makes the dyeing or printing process more expensive because of the expenditure of energy and apparatus and work requirements and prevents an uninterrupted course of work.
• the processing times in the heat treatment may actually be shortened by elevation of the temperature.
• this possibility cannot be utilized in general because the fiber properties of textured polyester materials are impaired.
• the mechanical conditions for the heat treatment, required for the removal of methylnaphthalene residues are not present.
• methylnaphthalene as a carrier for the dyeing of synthetic fibers has remained limited to but a few areas, even though the methylnaphthalene otherwise has advantageous properties as a carrier. These include outstanding colordeepening effect in the dyeing and printing of polyester fibers, good emulsifiability, even dyeing effect and reasonable price.
• the present invention relates therefor to a carrier composition, which contains methylnaphthalene and diphenylene oxide as the carrier-active substances, as well as a process for dyeing and printing of synthetic fibers, wherein this carrier composition is employed during the dyeing procedure.
• diphenylene oxide is equally a readily accessible commercial product.
• methylnaphthalene is understood to mean a-methylnaphthalene, B-methylnaphthalene or a mixture thereof.
• the weight ratio between methylnaphthalene and diphenylene oxide is normally in the range of 1.2:1 to 4:1 and preferably in the range of 1.5:1 to 3:1.
• novel carrier composition may be employed with success in all dyeing and printing methods which are known for the dyeing and printing of synthetic fibers such as polyesters, e.g., polyethylene glycol terephthalate, cellulose triacetate, polyvinyl chloride, polyacrylonitrile, polyolefins, such as isotactic polypropylene and other synthetic fibers or mixtures thereof with natural fibers.
• synthetic fibers such as polyesters, e.g., polyethylene glycol terephthalate, cellulose triacetate, polyvinyl chloride, polyacrylonitrile, polyolefins, such as isotactic polypropylene and other synthetic fibers or mixtures thereof with natural fibers.
• fiber encompasses staple fibers, for example, and also thread, thread skeins, woven and knitted textiles, foils, flocks and other materials consisting of said polymers which can be dyed and printed.
• the novel carrier composition may be added to the dye liquor in a dispersed or emulsified form or dissolved in an organic solvent.
• high-boiling organic solvents with a boiling point above C. are suitable, e.g., tetrahydronaphthalene, dimethylformamide, xylene, aromatic and aliphatic hydrocarbon halides such as benzene halides, esters such as benzene acid alkyl esters and alkylpolyglycol ethers.
• high-boiling petroleum distillates or mineral oils, as well as mixtures of various solvents may also be employed.
• high-boiling petroleum distillates particularly suitable is a transparent, non-toxic and weakly boiling distillate with a content of aromatic substances of about 99 by volume and a high flash point, which has a density of 0.877 g/cm and a boiling range of l62-180C.
• alkylpolyglycol ethers particularly applicable are ethyl, propyl, butyl and pentyl polyglycol ethers.
• the mixture of methylnaphthalene and diphenylene oxide is normally dissolved in sufficient solvent or solvent mixture to provide a weight ratio of solvent or solvent mixture to methylnaphthalene and diphenylene oxide of 4:1 to 0.5:1 preferably 2:1 to 1:1.
• aqueous emulsions of a mixture of methylnaphthalene and diphenylene oxide are obtained in the dye bath if an emulsifier is added to the solution of the mixture of methylnaphthalene and diphenylene oxide in organic solvent or solvent mixture.
• the novel carrier composition is easily emulsifiable in the dye bath even without special precautions and may be poured into the dye bath directly without the usually required preemulsification with water.
• anion-active substances include alkyl sulfates, e.g., sodium lauryl sulfate and sodium cetyl sulfate, turkey red oils, sulfonated oils, alkyl sulfonates and alkylaryl sulfates such as alkylbenzene sulfate and alkylnaphthalene sulfates.
• Nonionic reaction products include alkylene oxides with alkylphenols, alcohols, aliphatic saturated or unsaturated carboxylic acids, fatty amines and hydroxyl group'containing esters of saturated or unsaturated carboxylicacids.
• the preferred emulsifier compositions are those disclosed in German published Application Nos. 1,619,489 and 1,802,210. These emulsifier compositions consist of mixtures of three components hereinafter called Component 1, Component 11 and Component lll.
• Component I is an addition compound of alkylene oxides and, free hydroxyl groups containing esters of saturated orunsaturated aliphatic carboxylic acids or hydroxycarboxylic acids with polyvalent alcohols having2-6 hydroxyl groups.
• Component I may also be an addition compound of alkylene oxides and alkyl phenols.
• Component 11 includes alkali metal and/or alkaline earth metal saltsof alkylbenzene sulfonic acids.
• Component 11 includes aliphatic primary or secondary alcohols with 3-6 carbon atoms.
• the novel carrier composition is dispersed in the printing paste.
• the actual printing process is then carried out in a manner known per se.
• Drying of the dyeings or prints may be carried out under normal drying conditions, e.g., 30 seconds at 150C., without loss of fastness to light of the dyeings and prints. This is also true with respect to textured polyester material.
• EXAMPLE 1 a Five g. of a woven material consisting of polyethylene terephthalate fibers are treated in an aqueous dye bath at boiling temperature for l k hours in a liquor ratio of 1:40, the bath, based on the weight of the goods, containing 2 of the dispersion dyestuff of the formula as well as 3 g/l of a carrier preparation, which is obtained by simple stirring at room temperature, the following substances: i
• the blue dyeing obtained is then treated for reductive purification for 20 minutes at 85C. with a solution containing, in one liter water:
• both samples are dried for 30 seconds at 150C. after reductive purification and subsequently illuminated under the same conditions in a xeno-test apparatus.
• the dyeing (a), prepared using the novel carrier composition of this invention has a considerably better fastness to light than the dyeing (b) prepared with pure methylnaphthalene carrier.
• Disperse Red 60, Cl. Disperse Blue 73, Disperse Red 160, Disperse Violet 47, Disperse Blue 165, Disperse Orange -71 and the novel carrier compositions clearly better stabilities to light are obtained in the dyeing of polyester materials than when using methylnaphthalene as the carrier under comparable conditions.
• a carrier composition comprising a mixture of methylnaphthalene and diphenylene oxide in a weight ratio of 1.2:1 to 4:1.
• the carrier composition of claim 3 containing 5 to' 20% by weight emulsifier, based on the weight of the solution.
• the carrier composition of claim 3 containing 7 to mote the penetration of the dyestuff into the fibers, the 10% by weight emulsifier, based on the weight of the solution.

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

Applications Claiming Priority (1)

Publications (1)

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Family Applications (1)

Country Status (14)

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Citations (2)

• 1973
  • 1973-07-17 NL NL7309957A patent/NL7309957A/xx not_active Application Discontinuation
  • 1973-07-19 US US380534A patent/US3897207A/en not_active Expired - Lifetime
  • 1973-07-19 CA CA176,858A patent/CA1005951A/en not_active Expired
  • 1973-07-20 IN IN1709/CAL/73A patent/IN138846B/en unknown
  • 1973-07-24 ES ES417250A patent/ES417250A1/es not_active Expired
  • 1973-07-25 AT AT654473A patent/AT332849B/de not_active IP Right Cessation
  • 1973-07-25 IT IT27070/73A patent/IT992681B/it active
  • 1973-07-25 GB GB3534773A patent/GB1400135A/en not_active Expired
  • 1973-07-25 ZA ZA735069A patent/ZA735069B/xx unknown
  • 1973-07-25 NO NO3012/73A patent/NO132495C/no unknown
  • 1973-07-25 FR FR7327193A patent/FR2193865B1/fr not_active Expired
  • 1973-07-25 JP JP48083223A patent/JPS4992383A/ja active Pending
  • 1973-07-26 BE BE133919A patent/BE802850A/xx unknown
  • 1973-07-26 CH CH1095273A patent/CH545373A/de not_active IP Right Cessation

Patent Citations (2)

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