GB973821A - Production of artificial filamentary material of enhanced affinity for dyes - Google Patents

Production of artificial filamentary material of enhanced affinity for dyes

Info

Publication number
GB973821A
GB973821A GB41290/60A GB4129060A GB973821A GB 973821 A GB973821 A GB 973821A GB 41290/60 A GB41290/60 A GB 41290/60A GB 4129060 A GB4129060 A GB 4129060A GB 973821 A GB973821 A GB 973821A
Authority
GB
United Kingdom
Prior art keywords
phenyl
phosphate
bis
filaments
cellulose
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB41290/60A
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.)
Celanese Corp
Original Assignee
Celanese Corp
Celanese Corp of America
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 Celanese Corp, Celanese Corp of America filed Critical Celanese Corp
Publication of GB973821A publication Critical patent/GB973821A/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F1/00General methods for the manufacture of artificial filaments or the like
    • D01F1/02Addition of substances to the spinning solution or to the melt
    • D01F1/10Other agents for modifying properties
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S8/00Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
    • Y10S8/93Pretreatment before dyeing
    • Y10S8/931Washing or bleaching

Abstract

Filamentary material of improved dyeability is made from polymers normally yielding difficultly dyeable filaments by spinning filaments of individual denier not exceeding 25 from a composition comprising the polymer and a compatible ester as dyeing assistant, the ester being an aryl phosphate or a compound having the formula Ar.CO.O.R.Y.R.O.CO.Ar or the formula Ar. NH. CO. O.R.Y.R.O. CO. NH. Ar, where Ar is an aryl group, R is an alkylene group having up to 6 carbon atoms and Y is oxygen or sulphur so that the filaments contain the assistant throughout the entire filament cross-section in quantity sufficient to yield a product which, as compared with filaments containing no dyeing assistant but otherwise identical, has a dye take-up with a cellulose acetate disperse dye higher by at least 10% by weight and a safe, ironing temperature not reduced by more than 20 DEG C., and, in the case of cellulose ester products, not reduced to below 200 DEG C. Preferably, the filaments are of denier not greater than 7 and contain 3-15% by weight, based on the weight of filament, of dyeing assistant. Specified polymers include cellulose triesters, e.g. those of formic, acetic, propionic and butyric acids containing less than about 0.29 free hydroxyl groups per anhydro-glucose unit of the cellulose molecule, especially cellulose triacetate of acetyl value over 59%, expressed as acetic acid, linear polyesters of polyhydric alcohols (ethylene and diethylene glycols, dimethylol cyclohexane) with poly-carboxylic acids (terephthalic, isophthalic, phthalic, S-sulphoisophthalic and adipic acids) and linear polyesters of hydroxycarboxylic acids, e.g. polyglycolic acid. Cellulose triacetate and polyethylene terephthalate are especially suitable. Other specified polymers include polyamides especially poly (polymethylene) terephthalamides, adipamides and sebacamides in which the poly-methylene groups have 2-8 carbon atoms, e.g. polyhexamethylene adipamide and terephthalamide, polyaminocaproic acid derivatives, and polyurethanes, e.g. that formed from the bis-(chloroformate) of butane diol and tetramethylene diamine, acrylonitrile polymers and copolymers with over 40% acrylonitrile, vinylidene cyanide copolymers, and polyolefins, e.g. polypropylene. The filaments may be made by dry-spinning or melt-spinning. Preferred assistants are triaryl-phosphates, particularly o-phenyl phenyl bis-(phenyl) phosphate, which is especially suitable for use with cellulose triacetate, and tris(o-phenyl phenyl) phosphate which is especially suitable for polyethylene terephthalate. Others specified are triphenyl-, tricresyl-, tri(2, 5-dimethylphenyl)-, tri (2, 6 dimethylphenyl)-, tri (3, 5 dimethyl-phenyl)-, tri(2, 3, 5 trimethylphenyl) and tri (b -naphthyl) phosphates, dialkyl monoaryl phosphates, e.g. dimethyl monophenyl phosphate and diethyl monophenyl phosphate, diaryl monoalkyl phosphates, e.g. diphenyl monomethyl phosphate and dicresyl monomethyl phosphate, and the bis phosphates of alkylene glycols and dialkylene glycols, e.g. the bis (dicresyl phosphate) of di-ethylene glycol. Other specified assistants are bis-benzoates, e.g. diethylene glycol bis(benzoate) and the bis(benzoic acid) ester of di(b -hydroxy ethyl sulphide), diethylene glycol bis(phenyl urethane) and the bis(phenyl urethane) of di(b -hydroxyethyl) sulphide. Examples are given.ALSO:Filamentary material of improved dyeability is made from a composition comprising a polymer and a compatible ester as dyeing assistant, the ester being an aryl phosphate or a compound having the formula Ar. CO. O. R. Y. R. O. CO. Ar or the formula Ar. NH. CO. O. R. Y. R. O. CO. NH. Ar, where Ar is an aryl group, R is an alkylene group having up to 6 carbon atoms and Y is oxygen or sulphur so that the filaments contain the assistant throughout the entire filament cross-section. Specified polymers include cellulose triesters especially cellulose triacetate of acetyl value over 59%, expressed as acetic acid, linear polyesters of polyhydric alcohols (ethylene and diethylene glycols, dimethylol cyclohexane) with polycarboxylic acids (terephthalic, isophthalic, phthalic, S-sulphoisophthalic and adipic acids) and linear polyesters of hydroxycarboxylic acids, e.g. polyglycolic acid, polyamides especially poly (polymethylene) terephthalamides, adipamides and sebacamides, polyurethanes, acrylonitrile polymers and copolymers with over 40% acrylonitrile, vinylidene cyanide copolymers, and polyolefins, e.g. polypropylene. Preferred assistants are triarylphosphates, particularly o-phenyl phenyl bis (phenyl) phosphate, which is especially suitable for use with cellulose triacetate, and tris (o-phenyl phenyl) phosphate which is especially suitable for polyethylene terephthalate; others are specified. Examples are given.
GB41290/60A 1959-12-09 1960-12-01 Production of artificial filamentary material of enhanced affinity for dyes Expired GB973821A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US85832459A 1959-12-09 1959-12-09
US438813A US3330893A (en) 1959-12-09 1965-01-28 Method for increasing the dyeability of filamentary material

Publications (1)

Publication Number Publication Date
GB973821A true GB973821A (en) 1964-10-28

Family

ID=27031804

Family Applications (1)

Application Number Title Priority Date Filing Date
GB41290/60A Expired GB973821A (en) 1959-12-09 1960-12-01 Production of artificial filamentary material of enhanced affinity for dyes

Country Status (3)

Country Link
US (2) US3330893A (en)
DE (1) DE1469043A1 (en)
GB (1) GB973821A (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0421145D0 (en) * 2004-09-23 2004-10-27 Unilever Plc Laundry treatment compositions
CA2575589C (en) 2004-09-23 2013-11-12 Unilever Plc Laundry treatment compositions comprising hydrophobic dyes
DE102004051174A1 (en) * 2004-10-20 2006-05-04 BSH Bosch und Siemens Hausgeräte GmbH Lighting device for a water-conducting household appliance
US20080177089A1 (en) 2007-01-19 2008-07-24 Eugene Steven Sadlowski Novel whitening agents for cellulosic substrates
US8715368B2 (en) 2010-11-12 2014-05-06 The Procter & Gamble Company Thiophene azo dyes and laundry care compositions containing the same

Family Cites Families (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2397320A (en) * 1946-03-26 Plastic composition
US1217028A (en) * 1913-10-20 1917-02-20 Leon Lilienfeld Manufacture of artificial textile material and process of producing same.
US1116627A (en) * 1914-01-31 1914-11-10 Eastman Kodak Co Cellulose compound.
US1468609A (en) * 1922-11-16 1923-09-18 Columbia Graphophone Mfg Co Plastic composition of matter having a basis of cellulose ester
US1963974A (en) * 1928-07-31 1934-06-26 Celanese Corp Treatment of materials made of or containing cellulose esters or ethers
US1999405A (en) * 1930-05-20 1935-04-30 Dreyfus Henry Manufacture of plastic materials
US2021887A (en) * 1931-04-09 1935-11-26 Eastman Kodak Co Cellulose mixed ester composition
US2073629A (en) * 1932-10-19 1937-03-16 Celanese Corp Treatment of textile materials
US2099455A (en) * 1934-09-28 1937-11-16 Du Pont Cellulosic article of manufacture and method for preparing same
GB461593A (en) * 1935-03-06 1937-02-19 Degussa Improvements in and relating to processes for the manufacture of foils or films of cellulose tri-acetate
US2280863A (en) * 1938-12-24 1942-04-28 Hercules Powder Co Ltd Cellulose acetate molding composition
US2286041A (en) * 1938-12-24 1942-06-09 Hereules Powder Company Cellulose acetate molding composition
US2464784A (en) * 1945-08-09 1949-03-22 Gen Aniline & Film Corp Film forming solution of cellulose acetate
US2715763A (en) * 1950-06-27 1955-08-23 American Viscose Corp Synthetic textile fiber
US2612679A (en) * 1950-10-23 1952-10-07 Ladisch Rolf Karl Filaments containing fillers
US2591077A (en) * 1951-04-12 1952-04-01 Hercules Powder Co Ltd Method of producing a thermoplastic cellulose acetate composition
NL189028B (en) * 1954-07-07 Wella Ag METHOD OF REDUCING THE CONCENTRATION OF THE ACTIVE SUBSTANCES IN ALKALINE-REACTING COSMETIC PREPARATIONS.
US2982597A (en) * 1954-12-02 1961-05-02 Celanese Corp Textile treating
US3037956A (en) * 1955-06-10 1962-06-05 Onderzoekings Inst Res Process for extruding a fiber forming composition comprising a linear resinous condensate and a thickening agent
US2996466A (en) * 1956-01-07 1961-08-15 Onderzoekings Inst Res Process for preparing extruded high molecular weight substances and the resulting products
US2999056A (en) * 1956-10-04 1961-09-05 Du Pont Irradiation bonding of acidic compounds to shaped polymeric structures
US2924503A (en) * 1957-07-30 1960-02-09 Du Pont Process for melt spinning polyesters containing an alkaline earth sulfate filler
NL246911A (en) * 1958-03-06
US2965437A (en) * 1958-04-02 1960-12-20 Du Pont Process for wet spinning plasticized elastomeric polymers and subsequently removing the plasticizer
NL252702A (en) * 1959-06-16

Also Published As

Publication number Publication date
US3330893A (en) 1967-07-11
DE1469043A1 (en) 1968-11-07
US3172723A (en) 1965-03-09

Similar Documents

Publication Publication Date Title
US4035343A (en) Flame resistant synthetic linear polyesters and shaped structures made thereof
US5180793A (en) Flame resistant, low pilling polyester fiber
IE42101B1 (en) Process for the preparation of flame retarding linear polyesters
US3865783A (en) Flame-retardant polyester
US4548975A (en) Discoloration-resistant spandex fiber
US5382474A (en) Method for producing polyethylene terephthalate fibers with reduced flammability
US5750635A (en) Thermally stable polyesters formed utilizing antimony compounds as catalysts
US5145941A (en) Flame resistant, low pilling polyester fiber
GB1237310A (en) Novel polyamide and fibre thereof
GB973821A (en) Production of artificial filamentary material of enhanced affinity for dyes
US3874155A (en) Flame-retardant fiber blend
US3542737A (en) Polymeric polyesters containing alkylor alkenylsuccinic acids
US4504612A (en) Polyester antifume additive for spandex fiber
US4110301A (en) Polyester fiber dye stabilization
US3238178A (en) Elastomeric polymers stabilized with trialkylated phenol and thioor-ganic esters
US5238982A (en) Method for producing polyamide fibers with reduced flammability
US2952652A (en) Solutions of polyesters in substituted phosphoric amides and process for making same
US3833542A (en) Manufacture of thermally stabilized polyethylene terephthalate
US3464851A (en) Stabilized polyurethanes
US4102867A (en) Copolyesters of phthalic acids and hydantoins
US3085987A (en) Linear polyester containing a diaryl ether and process of producing same
US3669927A (en) Polycondensing bis(hydroxyalkyl) therephthalates in the presence of small amounts of a germanium compound and a sterically hindered bisphenol or trisphenol
US3776887A (en) Flame retardant polyester products prepared from halo-substituted-aryl-oxy-alkanols
JP2883778B2 (en) Method for producing flame-retardant polyester fiber
US3813454A (en) Flame-retardant polyesters