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GB1126321A - Method of producing polyvinyl alcohol fibre - Google Patents

Method of producing polyvinyl alcohol fibre

Info

Publication number
GB1126321A
GB1126321A GB572967A GB572967A GB1126321A GB 1126321 A GB1126321 A GB 1126321A GB 572967 A GB572967 A GB 572967A GB 572967 A GB572967 A GB 572967A GB 1126321 A GB1126321 A GB 1126321A
Authority
GB
United Kingdom
Prior art keywords
filaments
draw ratio
polyvinyl alcohol
aqueous solution
cooling
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
GB572967A
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.)
Kurashiki Rayon Co Ltd
Original Assignee
Kurashiki Rayon Co 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 Kurashiki Rayon Co Ltd filed Critical Kurashiki Rayon Co Ltd
Publication of GB1126321A publication Critical patent/GB1126321A/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
    • D01F6/02Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/14Monocomponent 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 unsaturated alcohols, e.g. polyvinyl alcohol, or of their acetals or ketals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Artificial Filaments (AREA)
  • Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)

Abstract

1,126,321. Wet spinning polyvinyl alcohol filaments. KURASHIKI RAYON K.K. 7 Feb., 1967 [8 Feb., 1966; 15 March, 1966 (2); 5 April, 1966], No. 5729/67. Heading B5B. Polyvinyl alcohol filaments are produced by wet spinning an aqueous solution of polyvinyl alcohol into a coagulating bath which is an aqueous solution of an inorganic salt and which is at a temperature above 55‹ C. and subjecting the filaments to cooling immediately after their being withdrawn from the bath, the cooling being effected at a temperature at least 30‹ C. below the temperature of the coagulating bath, and thereafter drawing the filaments in one or more stages at a draw ratio of not less than 4 : 1 and preferably not less than 6 : 1. The cooling may be effected by means of cold water and/or a cooled organic liquid, a cooled gas or cooling rolls. The concentration of the spinning solution may depend upon the average degree of polymerization of the polyvinyl alcohol used, the ranges of concentration being 20 to 50%, 15 to 45%, 10 to 40% and 8 to 35% corresponding to ranges of average D.P.s of 1000 to 1500, 1500 to 2000, 2000 to 3000 and 3000 to 5000 respectively. The organic cooling liquids which may be used include alcohols such as methanol and ethanol, acetone, esters, ethers and benzene. When a mixture of water and an organic liquid is used, the latter should be miscible with water. The salt present in the coagulating bath may be sodium, ammonium or zinc sulphate, sodium chloride or sodium carbonate. Two or more of these may be used conjointly. When sodium sulphate is used, the conjoint use therewith of potassium sulphate gives especially satisfactory results. In an example, a 15% aqueous solution of PVA of average DP 3000 is extruded into an aqueous solution of sodium sulphate at 80‹ C. and the filaments thereby formed are withdrawn from the coagulating bath, passed through water at 10‹ C., drawn by means of rolls at a draw ratio of 2 : 1 and further drawn at a draw ratio of 2 : 1 while wet with an aqueous solution of sodium sulphate at 60‹ C., the total draw ratio being 4 : 1. The filaments are then dried and drawn at a temperature of 235‹ C. and a draw ratio of 3 : 1, the overall draw ratio thus being 12 : 1. The filaments are thereafter heat set at 240‹ C. while being allowed to shrink 20%.
GB572967A 1966-02-08 1967-02-07 Method of producing polyvinyl alcohol fibre Expired GB1126321A (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP750266 1966-02-08
JP1625766 1966-03-15
JP1625866 1966-03-15
JP2165766 1966-04-05

Publications (1)

Publication Number Publication Date
GB1126321A true GB1126321A (en) 1968-09-05

Family

ID=27454729

Family Applications (1)

Application Number Title Priority Date Filing Date
GB572967A Expired GB1126321A (en) 1966-02-08 1967-02-07 Method of producing polyvinyl alcohol fibre

Country Status (3)

Country Link
DE (1) DE1669480A1 (en)
FR (1) FR1511205A (en)
GB (1) GB1126321A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112226840B (en) * 2020-08-04 2021-07-23 东华大学 A kind of high-strength and high-modulus PVA fiber and preparation method thereof

Also Published As

Publication number Publication date
DE1669480A1 (en) 1971-09-02
FR1511205A (en) 1968-01-26

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