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GB720380A - Improvements in the manufacture of filamentary material from copolymers of acrylonitrile and vinylidene chloride - Google Patents

Improvements in the manufacture of filamentary material from copolymers of acrylonitrile and vinylidene chloride

Info

Publication number
GB720380A
GB720380A GB79152A GB79152A GB720380A GB 720380 A GB720380 A GB 720380A GB 79152 A GB79152 A GB 79152A GB 79152 A GB79152 A GB 79152A GB 720380 A GB720380 A GB 720380A
Authority
GB
United Kingdom
Prior art keywords
filaments
per cent
copolymer
hydrocarbons
acetone
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
GB79152A
Inventor
John Downing
James Gordon Napier Drewitt
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.)
Acordis UK Ltd
Original Assignee
British Celanese Ltd
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 British Celanese Ltd filed Critical British Celanese Ltd
Priority to GB79152A priority Critical patent/GB720380A/en
Publication of GB720380A publication Critical patent/GB720380A/en
Expired legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H04ELECTRIC COMMUNICATION TECHNIQUE
    • H04JMULTIPLEX COMMUNICATION
    • H04J1/00Frequency-division multiplex systems
    • H04J1/02Details
    • H04J1/04Frequency-transposition arrangements
    • H04J1/045Filters applied to frequency transposition
    • 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
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/02Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/08Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polymers of halogenated hydrocarbons
    • D01F6/10Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polymers of halogenated hydrocarbons from polyvinyl chloride or polyvinylidene chloride

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Textile Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Electromagnetism (AREA)
  • Computer Networks & Wireless Communication (AREA)
  • Signal Processing (AREA)
  • Artificial Filaments (AREA)

Abstract

Artificial filaments are obtained by extruding an acetone solution of an acetone-soluble copolymer of acrylonitrile and vinylidene chloride into a coagulating bath of which at least 83 per cent by weight consists of one or more hydrocarbons. Single filaments, multifilament twisted and untwisted yarns, tow, bristles and like filamentary material may be obtained. The filaments are preferably subjected to stretching so as to increase the tensile strength, and they may also be heated first under tension and then while free to shrink so as to improve the extensibility and dimensional stability. The coagulating bath preferably comprises an aliphatic hydrocarbon, but an aromatic hydrocarbon such as benzene, toluene, xylene or solvent naphtha may be used. Hydrocarbons of boiling points above 120 DEG C. are suitable but mixtures of aliphatic hydrocarbons boiling within the range 150-300 DEG C., e.g. commercial kerosene, are preferred. The hydrocarbons may contain up to 20 per cent of their weight of a solvent or swelling agent for the polymer. The copolymer preferably contains 20-50 per cent by weight of acrylonitrile. It may be obtained by the methods described in Specification 643,198. The copolymer may be used in solution in pure acetone or in acetone containing a small proportion of water or methyl, ethyl or isopropyl alcohol. The concentration of the copolymer in the spinning solution may be 15-32 per cent. and the temperature of extrusion may be room temperature or higher, e.g. 60-85 DEG C. The coagulating bath may be at room or higher temperature, e.g. up to 90 DEG C., and it may be quiescent or may move in the same or opposite direction to that of the filaments. The filaments may be elongated during their travel through the bath, and on leaving the bath may be washed with petrol, ether or other volatile liquid until free from the coagulating liquid. The filaments may be stretched at temperatures of 120-210 DEG C. while or immediately after passing over heated surfaces, or through hot air or hot liquids. Following the stretching the filaments may be set by heating them at 150-190 DEG C. while under tension and may then be heated while under little or no tension. To avoid darkening of the filaments as a result of the heat treatment, a stabilizer may be incorporated in the copolymer which is used in preparing the spinning solution. The proportion of stabilizer may be 0.1-2 per cent of the weight of the polymer. Numerous stabilizers are specified, e.g. lead orthosilicate, phthalate, and stearate, zinc stearate, dibutyl tin laurate, calcium stearate, cadmium 2-ethyl-hexoate, barium stearate, epoxy-propyl ethers of bis-phenols, endo - methylene tetra - hydrophthalic acid, maleic acid, butyrolactone, 2,3,5-trichloro-21-hydroxybenzophenone and phenyl salicylate. Specifications 674,323 and 709,995 also are referred to.
GB79152A 1952-01-10 1952-01-10 Improvements in the manufacture of filamentary material from copolymers of acrylonitrile and vinylidene chloride Expired GB720380A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB79152A GB720380A (en) 1952-01-10 1952-01-10 Improvements in the manufacture of filamentary material from copolymers of acrylonitrile and vinylidene chloride

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB79152A GB720380A (en) 1952-01-10 1952-01-10 Improvements in the manufacture of filamentary material from copolymers of acrylonitrile and vinylidene chloride

Publications (1)

Publication Number Publication Date
GB720380A true GB720380A (en) 1954-12-15

Family

ID=9710561

Family Applications (1)

Application Number Title Priority Date Filing Date
GB79152A Expired GB720380A (en) 1952-01-10 1952-01-10 Improvements in the manufacture of filamentary material from copolymers of acrylonitrile and vinylidene chloride

Country Status (1)

Country Link
GB (1) GB720380A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1186977B (en) * 1959-07-30 1965-02-11 Crylor Fa Process for improving the stretchability of threads made of polymers based on acrylonitrile
US3491179A (en) * 1967-01-03 1970-01-20 American Cyanamid Co Preparation of acrylonitrile polymer fibers

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1186977B (en) * 1959-07-30 1965-02-11 Crylor Fa Process for improving the stretchability of threads made of polymers based on acrylonitrile
US3491179A (en) * 1967-01-03 1970-01-20 American Cyanamid Co Preparation of acrylonitrile polymer fibers

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