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GB979342A - Production of filamentary materials from difficultly meltable condensation polymers - Google Patents

Production of filamentary materials from difficultly meltable condensation polymers

Info

Publication number
GB979342A
GB979342A GB646661A GB646661A GB979342A GB 979342 A GB979342 A GB 979342A GB 646661 A GB646661 A GB 646661A GB 646661 A GB646661 A GB 646661A GB 979342 A GB979342 A GB 979342A
Authority
GB
United Kingdom
Prior art keywords
filaments
coagulant
sulphuric acid
solution
groups
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
GB646661A
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
Priority claimed from US83981A external-priority patent/US3227793A/en
Application filed by Celanese Corp, Celanese Corp of America filed Critical Celanese Corp
Publication of GB979342A publication Critical patent/GB979342A/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
    • D01F6/58Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
    • D01F6/60Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyamides

Landscapes

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

Abstract

979,342. Synthetic filaments. CELANESE CORPORATION OF AMERICA. Feb. 22, 1961 [Feb. 25, 1960; Jan. 23, 1961], No. 6466/61. Heading B5B. Filamentary materials are made from difficultly meltable synthetic linear polymers having repeating -CO.NR- groups in the molecule, where R is hydrogen or a monovalent organic radical, by extruding a solution of such a polymer in sulphuric acid of at least 80% by weight concentration through an orifice into an acidic liquid coagulant to form the filamentary material, stretching it while still swollen with sulphuric acid and thereafter washing free from sulphuric acid and drying the stretched product. Difficultly meltable polymers include polyamides melting above 275‹ C., polyurethanes and polyureas melting above 179‹ C., especially above 210‹ C., and in general polymers containing cyclic groups, e.g. m- and p-phenylene cycloalkylene groups, e.g. 1,4-cyclohexylene and/or heterocyclic groups, e.g. piperazylene, as an integral part of the chain. A long list of suitable polymers is given. The polymer may be a polyamide melting above 275‹ C., preferably a poly-(polymethylene) terephthalamide in which the polymethylene groups contain 2-10 carbon atoms, e.g. polyhexamethylene terephthalamide, and may be dissolved in sulphuric acid of 95-100% concentration to give a polymer solution of 5-30% by weight concentration. A spinning temperature between 20‹ C. and 100‹ C. is preferred. Aqueous sulphuric acid of 40-60% by weight concentration may be used as the coagulant, maintained at 40- 60‹ C., the coagulant temperature and concentration being such as to fall within the closed area between curves A and B in Fig. 1. Aqueous formic and acetic acids may also be used as coagulants, suitably in concentrations of 52-68% by weight and 52% to 63% by weight respectively at temperatures of about 20‹ C., or in lower concentrations at higher temperatures. After being withdrawn from the coagulant the filaments may be further stretched in water or aqueous sulphuric acid of up to 30% by weight concentration at temperatures up to the boiling point of the solution. After washing free from acid, filaments may also be stretched in air while heated to an elevated temperature. Other liquid heating media which may be used for stretching include tetralin, toluene, heptane, benzene, methanol, methanol/ water mixtures, acetone, acetone/water mixtures and ethylene glycol. The filaments may subsequently be annealed, e.g. polyhexamethylene terephthalamide filaments may be annealed at 270‹ C. for a period of 5 minutes. In a preferred method, the solution is extruded downwards into the coagulant to form filaments which are passed round a guide where the filaments are substantially coagulated and are drawn upwards and out of the coagulant so as to stretch the filaments, the guide preventing the tension in the filaments passing back to the material leaving the extrusion orifice to an extent sufficient to cause breakage. In Fig. 2, spinning solution is supplied through pipe 10 to spinneret 11, below the surface of the coagulant 12. The filaments formed are pulled around guide 15 and taken up by the positivelydriven godet roll 16. The angle α may be varied from 5-70 degrees and the distance A varied from 12-100 inches, being preferably from 20-70 inches. Filaments of poly-(polymethylene) terephthalamides melting above 275‹ C. and having a tensile factor of at least 10, e.g. polyhexamethylene terephthalamides having tensile factors of from 10 to 25 may be made by the process of the invention. Specification 977,405 is referred to.
GB646661A 1960-02-25 1961-02-22 Production of filamentary materials from difficultly meltable condensation polymers Expired GB979342A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US1109460A 1960-02-25 1960-02-25
US83981A US3227793A (en) 1961-01-23 1961-01-23 Spinning of a poly(polymethylene) terephthalamide

Publications (1)

Publication Number Publication Date
GB979342A true GB979342A (en) 1965-01-01

Family

ID=26681986

Family Applications (1)

Application Number Title Priority Date Filing Date
GB646661A Expired GB979342A (en) 1960-02-25 1961-02-22 Production of filamentary materials from difficultly meltable condensation polymers

Country Status (3)

Country Link
BE (1) BE600587A (en)
DE (1) DE1222621B (en)
GB (1) GB979342A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1810426A1 (en) * 1968-06-12 1970-02-12 Du Pont Mass and fibers or threads made from it
DE2219703A1 (en) * 1971-04-28 1972-11-09 E.I. Du Pont De Nemours And Co., Wilmington, Del. (V.St.A.) Polyamide fibers and films and processes for making the same
FR2178772A1 (en) * 1972-03-08 1973-11-16 Inst Iskusstvennogo Volokna Heat-resistant fibres - based on completely aromatic polyamides contg heterocycles in the molecule, prepd by wet-spinning
US4702876A (en) * 1984-07-11 1987-10-27 Akzo N.V. Variable-aperture process for the manufacture of filaments from aromatic polyamides

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB542034A (en) * 1940-06-21 1941-12-23 Henry Dreyfus Improvements in or relating to artificial filaments, films and like materials
US2360406A (en) * 1940-06-21 1944-10-17 Celanese Corp Manufacture of artificial filaments, films, and like materials
DE929578C (en) * 1942-08-06 1955-07-04 Bayer Ag Process for the production of linear polycondensation products
CH262562A (en) * 1946-11-01 1949-07-15 Tootal Broadhurst Lee Co Ltd Process for the concentration of solutions of synthetic linear polyamides in mineral acids.
BE537046A (en) * 1954-03-23

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1810426A1 (en) * 1968-06-12 1970-02-12 Du Pont Mass and fibers or threads made from it
FR2010753A1 (en) * 1968-06-12 1970-02-20 Du Pont
DE1929694A1 (en) * 1968-06-12 1970-09-03 Du Pont Mass and items made from it
DE1929694B2 (en) 1968-06-12 1976-04-22 E.I. du Pont de Nemours 'and Co., Wilmington, Del. (V.St.A.) OPTICALLY ANISOTROPIC MASSES OF AROMATIC POLYAMIDES
DE2219703A1 (en) * 1971-04-28 1972-11-09 E.I. Du Pont De Nemours And Co., Wilmington, Del. (V.St.A.) Polyamide fibers and films and processes for making the same
FR2134582A1 (en) * 1971-04-28 1972-12-08 Du Pont
DE2265806C3 (en) * 1971-04-28 1991-03-07 E.I. Du Pont De Nemours & Co., Wilmington, Del., Us
FR2178772A1 (en) * 1972-03-08 1973-11-16 Inst Iskusstvennogo Volokna Heat-resistant fibres - based on completely aromatic polyamides contg heterocycles in the molecule, prepd by wet-spinning
US4702876A (en) * 1984-07-11 1987-10-27 Akzo N.V. Variable-aperture process for the manufacture of filaments from aromatic polyamides

Also Published As

Publication number Publication date
BE600587A (en)
DE1222621B (en) 1966-08-11

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