GB709995A - Improvements relating to the manufacture of textile materials - Google Patents

Improvements relating to the manufacture of textile materials

Info

Publication number
GB709995A
GB709995A GB8419/51A GB841951A GB709995A GB 709995 A GB709995 A GB 709995A GB 8419/51 A GB8419/51 A GB 8419/51A GB 841951 A GB841951 A GB 841951A GB 709995 A GB709995 A GB 709995A
Authority
GB
United Kingdom
Prior art keywords
per cent
copolymer
filaments
minutes
stearate
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
GB8419/51A
Inventor
Noel Arthur Hampson
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 GB8419/51A priority Critical patent/GB709995A/en
Publication of GB709995A publication Critical patent/GB709995A/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
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/28Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/40Modacrylic fibres, i.e. containing 35 to 85% acrylonitrile
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/022Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the choice of material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
    • B29C48/05Filamentary, e.g. strands
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2105/00Condition, form or state of moulded material or of the material to be shaped
    • B29K2105/0058Liquid or visquous
    • B29K2105/0073Solution
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2313/00Use of textile products or fabrics as reinforcement
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29LINDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
    • B29L2031/00Other particular articles
    • B29L2031/726Fabrics

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Textile Engineering (AREA)
  • Artificial Filaments (AREA)

Abstract

Artificial filaments are made by extruding and solidifying by the removal of solvent an acetone solution of a vinylidene chlorideacrylonitrile copolymer containing 20-50, and especially 40-48 per cent., by weight of acrylonitrile, stretching the filaments by 300-2,000 per cent. of their original length at over 120 DEG C., heating them to 150 DEG C. or over while preventing shrinkage and then heating them to 150 DEG C. or over while allowing them to shrink freely or to a controlled degree. The copolymer may be made by copolymerizing the monomers in an aqueous medium, the initial amount of water present being 2-10 times the total weight of the two monomers as described in Specification 643,198. The acetone used may be pure or may contain up to 7.5 per cent. of water and/or an alcohol boiling below 120 DEG C., especially methyl, ethyl or isopropyl alcohol. The solution may contain about 18-32 per cent. of the copolymer and may be extruded into a current of an evaporative medium at 20-27 DEG C. but preferably 60-80 DEG C. After leaving the spinning cell the filaments may be quickly washed with water before being wound up or stretched. The stretching of the filaments is preferably carried out at about 150 DEG -200 DEG C., and especially about 175 DEG -195 DEG C., and they are preferably stretched to 500-1,000 per cent. of the initial length. The setting or annealing stage following the stretching may be carried out at about 150 DEG -190 DEG C., especially 165 DEG -190 DEG C. for 2-5 minutes. The heating in both stages may be carried out by means of an inert fluid such as air, steam or water under pressure, a mineral oil or a glycol or glycerol, or by radiation. The heating of the set filaments under little or no tension may be carried out for about 2 minutes or more at the setting temperature or at a higher temperature up to about 195 DEG -200 DEG C., or at a temperature not more than about 25 DEG C. below the setting temperature, preferably for about 3-7 minutes. The filaments are preferably dry-spun, but may be wet-spun, e.g. by extruding the spinning solution into an aqueous coagulating bath containing a swelling agent for the copolymer such as acetone or another lower aliphatic ketone. Alternatively the bath may contain water-soluble metal thiocyanates. The freshly coagulated material may be stretched during the spinning. The copolymers may be colourstabilized by the addition of 0.1-2 per cent. of lead orthosilicate, phthalate, stearate or naphthenate, zinc stearate or naphthenate, dibutyl tin laurate, stearate or naphthenate, di-alkyl di-alkoxy compounds of tin such as dibutyl dibutoxy tin, calcium acetoacetate and stearate, cadmium 2-ethyl-hexoate, barium stearate, strontium naphthenate; epoxides such as epoxy-propyl ethers of bis-phenols, e.g. 4, 41-bis-(2, 3-epoxypropoxy)-diphenyl, endomethylene tetrahydrophthalic acid, 1, 11-diphenyl-diethyl ether, maleic acid and derivatives thereof, butyro-lactone, 2, 3, 5-trichloro21-hydroxy-benzophenone, 2, 21-dihydroxybenzophenone, alkaline earth metal salts of chlorinated hydroxy-benzophenones, phenyl salicylate and alkyl-phenyl salicylates such as t-butyl-salol. In an example 22 parts (by weight) of a copolymer of 45 per cent. by weight of acrylonitrile and 55 per cent. of vinylidene chloride (prepared in a described manner) are dissolved in 71.5 parts of acetone, 3.7 parts of methylated spirit and 2.8 parts of water, and the solution is heated to about 75 DEG C. and extruded downwardly into an upwardly flowing air stream at room temperature. The filaments produced are formed into a yarn with a low degree of twist which is stretched at 180 DEG C. by 600 per cent. of its length, heated at p constant length for 3 minutes at 185 DEG C. and heated without tension at 185 DEG C. for 5 minutes. In all the examples one per cent. of stabilizer such as dibutyl tin laurate may be incorporated in the copolymer. Specification 674,323 also is referred to. The Provisional Specification states that the copolymer may contain 30-60 per cent. of acrylonitrile.
GB8419/51A 1951-04-11 1951-04-11 Improvements relating to the manufacture of textile materials Expired GB709995A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB8419/51A GB709995A (en) 1951-04-11 1951-04-11 Improvements relating to the manufacture of textile materials

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB8419/51A GB709995A (en) 1951-04-11 1951-04-11 Improvements relating to the manufacture of textile materials

Publications (1)

Publication Number Publication Date
GB709995A true GB709995A (en) 1954-06-02

Family

ID=9852160

Family Applications (1)

Application Number Title Priority Date Filing Date
GB8419/51A Expired GB709995A (en) 1951-04-11 1951-04-11 Improvements relating to the manufacture of textile materials

Country Status (1)

Country Link
GB (1) GB709995A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4140844A (en) * 1976-12-24 1979-02-20 Bayer Aktiengesellschaft Polyacrylonitrile filament yarns
FR2746820A1 (en) * 1996-03-28 1997-10-03 Hyun Paik Bo New synthetic yarn used for the clothes industry

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4140844A (en) * 1976-12-24 1979-02-20 Bayer Aktiengesellschaft Polyacrylonitrile filament yarns
FR2746820A1 (en) * 1996-03-28 1997-10-03 Hyun Paik Bo New synthetic yarn used for the clothes industry

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