US2833738A - Method of producing a spinning solution of an acrylonitrile polymer - Google Patents

Method of producing a spinning solution of an acrylonitrile polymer Download PDF

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Publication number
US2833738A
US2833738A US437285A US43728554A US2833738A US 2833738 A US2833738 A US 2833738A US 437285 A US437285 A US 437285A US 43728554 A US43728554 A US 43728554A US 2833738 A US2833738 A US 2833738A
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US
United States
Prior art keywords
spinning solution
weight
producing
glycolic acid
acid nitrile
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 - Lifetime
Application number
US437285A
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English (en)
Inventor
Pirot Ernst
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.)
VER GLANZTOFF FABRIKEN AG
VEREINIGTE GLANZTOFF-FABRIKEN AG
Original Assignee
VER GLANZTOFF FABRIKEN AG
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
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Application filed by VER GLANZTOFF FABRIKEN AG filed Critical VER GLANZTOFF FABRIKEN AG
Application granted granted Critical
Publication of US2833738A publication Critical patent/US2833738A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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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
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00Compositions 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; Compositions of derivatives of such polymers
    • C08L33/18Homopolymers or copolymers of nitriles
    • C08L33/20Homopolymers or copolymers of acrylonitrile
    • 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
    • D01F6/18Monocomponent 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 nitriles, e.g. polyacrylonitrile, polyvinylidene cyanide
    • 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
    • D01F6/38Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds comprising unsaturated nitriles as the major constituent
    • 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
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L29/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical; Compositions of hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Compositions of derivatives of such polymers
    • C08L29/10Homopolymers or copolymers of unsaturated ethers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L31/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid; Compositions of derivatives of such polymers
    • C08L31/02Homopolymers or copolymers of esters of monocarboxylic acids
    • C08L31/04Homopolymers or copolymers of vinyl acetate

Definitions

  • This invention relates. to a process for producing a spinning solution from polyacrylonitrile or copolymers thereof.
  • Example 1 200 g of polyacrylonitrile having a K-value of were stirred in 800 g of a solvent mixture consisting of 80 percent by Weight of glycolic acid nitrile and 20 percent by weight of methylene glycol diacetate, at a temperature of about 15 C., to form a suspension. While the suspension was stirred, it was deaerated in a vacuum. After about one hour the deaerated mixture was heated gradually to a temperature ranging between and C. and stirring was continued for another hour at this temperature.
  • the spinning solution thus obtained was found to be satisfactory in every way and was then spun continuously according to the dry-spinning method.
  • the threads or filaments were stretched in hot condition in two steps, to from 8 to 10 times their original length. These threads or filaments were found to present a particularly uniform cross-section and to display a favorable strength of about 40 breaking km. at an elongation of between 7 and 8 percent.
  • Example 2 200 g of a copolymer consisting of 90 percent by weight of acrylonitrile and 10 percent of acrylic acid amide were stirred in cold condition together with 800 g of a solvent mixture containing 75 percent by weight of glycolic acid nitrile and 25 percent by weight of methylene glycol dibutyrate, to form a suspension which was then Worked up, in accordance with Example 1. On being spun the solution thus obtained proved very satisfactory and the threads or filaments produced from it had a particularly favorable strength of about 45 breaking km. at an elongation of about 8 percent.
  • n may be a numeral between 0 and 2.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Polymers & Plastics (AREA)
  • Textile Engineering (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Toxicology (AREA)
  • Dispersion Chemistry (AREA)
  • Artificial Filaments (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)
US437285A 1953-06-25 1954-06-16 Method of producing a spinning solution of an acrylonitrile polymer Expired - Lifetime US2833738A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE326493X 1953-06-25
DEV6481A DE1004340B (de) 1953-06-25 1953-11-06 Verfahren zur Herstellung von Faeden aus Polyacrylnitril bzw. seinen Mischpolymerisaten mit verbesserten textilen Eigenschaften

Publications (1)

Publication Number Publication Date
US2833738A true US2833738A (en) 1958-05-06

Family

ID=25807173

Family Applications (2)

Application Number Title Priority Date Filing Date
US437285A Expired - Lifetime US2833738A (en) 1953-06-25 1954-06-16 Method of producing a spinning solution of an acrylonitrile polymer
US466197A Expired - Lifetime US2851435A (en) 1953-06-25 1954-11-01 Method of improving the textile properties of polyacrylonitrile threads

Family Applications After (1)

Application Number Title Priority Date Filing Date
US466197A Expired - Lifetime US2851435A (en) 1953-06-25 1954-11-01 Method of improving the textile properties of polyacrylonitrile threads

Country Status (7)

Country Link
US (2) US2833738A (fr)
BE (2) BE528519A (fr)
CH (3) CH326493A (fr)
DE (1) DE1004340B (fr)
FR (3) FR1230409A (fr)
GB (3) GB752703A (fr)
NL (1) NL83932C (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7199176B2 (en) 1995-05-22 2007-04-03 Cabot Corporation Elastomeric compounds incorporating silicon-treated carbon blacks

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3379794A (en) * 1966-04-27 1968-04-23 Du Pont Blends of fiber forming acrylonitrile polymers and polymeric 2, 2-disubstituted propioleactone
DE2947824A1 (de) 1979-11-28 1981-07-23 Bayer Ag, 5090 Leverkusen Querschnittsstabile, hygroskopische kern/mantelstruktur aufweisende fasern und faeden und verfahren zu deren herstellung
DE3225268A1 (de) * 1982-07-06 1984-01-12 Bayer Ag, 5090 Leverkusen Kontinuierliches trockenspinnverfahren fuer hochschrumpffaehige acrylnitrilfaeden und -fasern
DE3225267A1 (de) * 1982-07-06 1984-01-12 Bayer Ag, 5090 Leverkusen Herstellung loesungsmittelarmer polyacrylnitril-spinnfaeden

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2620324A (en) * 1950-12-01 1952-12-02 Eastman Kodak Co Polymerization of acrylonitrile in the presence of amide polymers

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2123599A (en) * 1930-01-28 1938-07-12 Ig Farbenindustrie Ag Production of polymerization products
NL73540C (fr) * 1942-06-17
US2404725A (en) * 1944-11-18 1946-07-23 Du Pont Polymer solutions
US2571777A (en) * 1950-04-08 1951-10-16 Eastman Kodak Co Acrylonitrile polymer mixed with copolymer of vinyl acetate and isopropenyl acetate
US2571683A (en) * 1950-04-13 1951-10-16 Eastman Kodak Co Mixtures comprising polyacrylonitrile and a polyvinyl acetal
NL160413B (nl) * 1950-04-26 Int Computers Ltd Werkwijze voor het vervaardigen van een magneetkop.

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2620324A (en) * 1950-12-01 1952-12-02 Eastman Kodak Co Polymerization of acrylonitrile in the presence of amide polymers

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7199176B2 (en) 1995-05-22 2007-04-03 Cabot Corporation Elastomeric compounds incorporating silicon-treated carbon blacks

Also Published As

Publication number Publication date
CH326493A (de) 1957-12-31
US2851435A (en) 1958-09-09
DE1004340B (de) 1957-03-14
GB752507A (en) 1956-07-11
CH326494A (de) 1957-12-31
BE528519A (fr)
FR66290E (fr) 1956-06-28
CH329999A (de) 1958-05-15
GB754775A (en) 1956-08-15
FR1100646A (fr) 1955-09-22
GB752703A (en) 1956-07-11
FR1230409A (fr) 1960-09-15
NL83932C (fr)
BE528051A (fr)

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