GB712999A - Improvements in or relating to acrylonitrile polymer solutions - Google Patents

Improvements in or relating to acrylonitrile polymer solutions

Info

Publication number
GB712999A
GB712999A GB1438851A GB1438851A GB712999A GB 712999 A GB712999 A GB 712999A GB 1438851 A GB1438851 A GB 1438851A GB 1438851 A GB1438851 A GB 1438851A GB 712999 A GB712999 A GB 712999A
Authority
GB
United Kingdom
Prior art keywords
hydroxy
weight
per cent
propionitrile
cyano
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
GB1438851A
Inventor
John Downing
Arthur Hodge
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 GB1438851A priority Critical patent/GB712999A/en
Publication of GB712999A publication Critical patent/GB712999A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/02Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
    • C08J3/09Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids
    • C08J3/091Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids characterised by the chemical constitution of the organic liquid
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2333/00Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
    • C08J2333/18Homopolymers or copolymers of nitriles
    • C08J2333/20Homopolymers or copolymers of acrylonitrile

Landscapes

  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Artificial Filaments (AREA)

Abstract

Solutions suitable for the manufacture of fibres and filaments comprise an acrylonitrile polymer dissolved in an anhydrous mixture comprising 60-95 per cent. by weight if nitromethane and 40-50 per cent. by weight of one or more compounds selected from lactones of hydroxy-fatty acids, alkylene cyclic carbonates, cyclic anhydrides of saturated aliphatic dicarboxylic acids, beta-nitro-and -cyano-ethanols, nitro- and cyano-substituted higher homologues of ethanol containing one further polar substituent atom or group for each carbon atom in excess of two in the nitro- or cyano-substituted alkanol, and unsaturated aliphatic acids of dissociation constant above 2 x 10-3 at 25 DEG C.; or a mixture comprising less than 50 per cent. by weight of nitromethane and more than 50 per cent. by weight of a cyclic anhydride of an aliphatic unsaturated dicarboxylic acid. Compounds specified are butyrolactone, valerolactone, glycol carbonate, succinic, glutaric and maleic anhydrides, 3-hydroxy- 2-chloro-propionitrile, 3 - chloro - 2 - hydroxy - propionitrile, 3, 3 - dichloro - 2 - methyl - 2 - hydroxy - propionitrile, and maleic acid. The acrylonitrile polymer may be polycrylonitrile and copolymers of acrylonitrile with vinyl chloride, vinylidene chloride, vinyl acetate, methyl or phenyl acrylate, or styrene. The fibres and films may be made by dry or wet-spinning or wet-casting techniques such as those described in Specification 712,984 and the fibres oriented by stretching, e.g. as described in Specification 636,476. The solutions may also be used in the production of coatings. Specifications 676,889 and 712,998 also are referred to.
GB1438851A 1950-06-29 1950-06-29 Improvements in or relating to acrylonitrile polymer solutions Expired GB712999A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1438851A GB712999A (en) 1950-06-29 1950-06-29 Improvements in or relating to acrylonitrile polymer solutions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1438851A GB712999A (en) 1950-06-29 1950-06-29 Improvements in or relating to acrylonitrile polymer solutions

Publications (1)

Publication Number Publication Date
GB712999A true GB712999A (en) 1954-08-04

Family

ID=10040287

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1438851A Expired GB712999A (en) 1950-06-29 1950-06-29 Improvements in or relating to acrylonitrile polymer solutions

Country Status (1)

Country Link
GB (1) GB712999A (en)

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