[go: up one dir, main page]

US2851435A - Method of improving the textile properties of polyacrylonitrile threads - Google Patents

Method of improving the textile properties of polyacrylonitrile threads Download PDF

Info

Publication number
US2851435A
US2851435A US466197A US46619754A US2851435A US 2851435 A US2851435 A US 2851435A US 466197 A US466197 A US 466197A US 46619754 A US46619754 A US 46619754A US 2851435 A US2851435 A US 2851435A
Authority
US
United States
Prior art keywords
threads
polyacrylonitrile
improving
polyvinylacetate
solution
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
US466197A
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.)
Glanzstoff AG
Vereinigte Glanzstoff Fabriken AG
Original Assignee
Glanzstoff 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
Publication date
Application filed by Glanzstoff AG filed Critical Glanzstoff AG
Application granted granted Critical
Publication of US2851435A publication Critical patent/US2851435A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00—Processes of treating or compounding macromolecular substances
    • C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
    • C08J3/09—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids
    • C08J3/091—Making 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
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00—Compositions 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
    • C08L33/18—Homopolymers or copolymers of nitriles
    • C08L33/20—Homopolymers or copolymers of acrylonitrile
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/02—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/18—Monocomponent 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
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/28—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/38—Monocomponent 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
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2333/00—Characterised 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
    • C08J2333/18—Homopolymers or copolymers of nitriles
    • C08J2333/20—Homopolymers or copolymers of acrylonitrile
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L29/00—Compositions 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
    • C08L29/10—Homopolymers or copolymers of unsaturated ethers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L31/00—Compositions 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
    • C08L31/02—Homopolymers or copolymers of esters of monocarboxylic acids
    • C08L31/04—Homopolymers or copolymers of vinyl acetate

Definitions

  • This invention relates to polyacrylonitrile type fibers, and more particularly to a method of improving the textile properties of threads and filaments spun from a solution of polyacrylonitrile or copolymers thereof.
  • Prior proposals of this kind included a process of improving the mechanical properties of threads or filaments spun from solutions of polyacrylonitrile or its copolymers which consisted in adding to the spinning solution, directly before it was spun, a certain quantity of polyvinylacetate.
  • This process made it possible to produce threads or filaments devoid of the tendency to split into fibrillae, which is known to quite particularly reduce the resistivity of the threads against abrasion. In this process from 2 to 30% and preferably from 5 to 15% polyvinylacetate calculated on the solid substance content of the spinning solution were added.
  • polyvinylacetate and polyvinyl ethyl ether at the rate of 2 to 30% and preferably about 15% of the solid matter content of the spinning solution, thus allowing from 98 to 70% of such solid matter content for polyacrylonitrile.
  • a spinning solution of polyacrylonitrile or a coploymer thereof in a solvent for example in dimethylformamide.
  • a mixture of e. g. polyvinylacetate and about 5% polyvinylethylether is added either in solid form or in solution, for example in dimethylformamide.
  • the complete mixture is heated to about 110 C. and spun at about 100 C. in the usual manner.
  • Example 1 To 18.7 kg. polyacrylonitrile having a K-value of about 85 were added 2.2 kg. polyvinylacetate having a K-value of about 70 and 1.1 kg. polyvinylethylether having a K- value of about 50, the whole mixture being dissolved in 78 kg. dimethylformamide. This solution was dissolved under stirring in the solvent by heating to 110 C. The solution was then filtered and cooled down to 80 C. before being spun according to the dry or wet spinning process.
  • the spinning solution was spun from a spinning nozzle having perforations of about 125 to 250 t through a heated tube about 4meters long.
  • the solvent is substantially removed from the bundle of threads by means of a hot air current of about 180 C. traversing the tube.
  • the bundle of threads is caused to issue from the nozzle, for example, into a bath of glycerine heated to about Bil-140 C.
  • the threads recovered in this process are particularly well adapted for being stretched up to twelve times their lengths. After having been shrunk again, they have a strength value of 38 Rkm. at about 20% elongation. Their resistivity against abrasion is about 6 times that of threads formed from the same material, however, without any addition as shown e. g. by the following tests.
  • abrasion tours points to the practice of pressing a rotating cylinder of Carborundum repeatedly against a thread and counting the number of revolutions before breakage.
  • the feel of the threads last soft and supple.
  • Example 2 17 kg. polyacrylonitrile having a K-value of about 90, 1.8 kg. polyvinylacetate having a K-value of about and 1.2 kg. polyvinylethylether having a K-value of about 50 were dissolved in kg. dimethylformamide and spun according to Example 1. After stretching there were obtained threads of great suppleness which had a breaking strength of up to 40 Rkm. at an elongation of 20-25%. These threads had a very soft feel.
  • the method of improving the textile properties of threads of polyacrylonitrile type polymers which comprises dissolving from 98 to 70 percent by weight of polyacrylonitrile, and from 2 to 30 percent by weight of a mixture in the proportion of from 2:1 to 1.5 :1, of polyvinylacetate and polyvinylethylether, in dimethylformamide, and spinning the solution thus obtained.
  • the method of improving the textile properties of threads of polyacrylonitrile type polymers which comprises dissolving about percent by weight of polyacrylonitrile, and about 15 percent by weight of a mixture in the proportion of from about 2:1, of polyvinylacetate and polyvinylethylether, in dimethylformamide, and spinning the solution thus obtained.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Polymers & Plastics (AREA)
  • Medicinal Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Dispersion Chemistry (AREA)
  • Toxicology (AREA)
  • Artificial Filaments (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)

Description

United States Patent METHOD OF IMPROVING THE TEXTILE PROP- ERTIES 0F PfiLYACRYLONITRILE THREADS No Drawing. Application November 1, 1954 Serial No. 466,197
Claims priority, application Germany November 6, 1953 2 Claims. (Cl. 260-326) This invention relates to polyacrylonitrile type fibers, and more particularly to a method of improving the textile properties of threads and filaments spun from a solution of polyacrylonitrile or copolymers thereof.
Prior proposals of this kind included a process of improving the mechanical properties of threads or filaments spun from solutions of polyacrylonitrile or its copolymers which consisted in adding to the spinning solution, directly before it was spun, a certain quantity of polyvinylacetate. This process made it possible to produce threads or filaments devoid of the tendency to split into fibrillae, which is known to quite particularly reduce the resistivity of the threads against abrasion. In this process from 2 to 30% and preferably from 5 to 15% polyvinylacetate calculated on the solid substance content of the spinning solution were added.
I have now found that apart from this improvement of the resistivity against abrasion, I can also obtain an improvement of the feel by adding to the polyacrylonitrile or a copolymer thereof, before it is spun, in addition to the polyvinylacetate, also a certain quantity of polyvinyl ethyl ether.
I prefer adding polyvinylacetate and polyvinyl ethyl ether at the rate of 2 to 30% and preferably about 15% of the solid matter content of the spinning solution, thus allowing from 98 to 70% of such solid matter content for polyacrylonitrile. I have obtained the best effects when adding the two substances, to wit: polyvinylacetate and polyvinylethylether, in the proportion of 2 to 1 calculated on the total quantity of 2-30%.
In practicing this process there is first prepared a spinning solution of polyacrylonitrile or a coploymer thereof in a solvent, for example in dimethylformamide. To this solution a mixture of e. g. polyvinylacetate and about 5% polyvinylethylether is added either in solid form or in solution, for example in dimethylformamide. The complete mixture is heated to about 110 C. and spun at about 100 C. in the usual manner.
Example 1 To 18.7 kg. polyacrylonitrile having a K-value of about 85 were added 2.2 kg. polyvinylacetate having a K-value of about 70 and 1.1 kg. polyvinylethylether having a K- value of about 50, the whole mixture being dissolved in 78 kg. dimethylformamide. This solution was dissolved under stirring in the solvent by heating to 110 C. The solution was then filtered and cooled down to 80 C. before being spun according to the dry or wet spinning process.
The K-Value mentioned in this example is defined on pages 58-64 of the book by Fikentscher entitled Cellulosechemie" (1932) and in German Plastics Practice, a
record rewritten and amplified from the Quartermasters Reports by John M. De Bell, William C. Goggin, Walter E. Gloor, published by De Bell and Richardson, Springfield, Mass, 1946, pages 518-521.
In the dry spinning process the spinning solution was spun from a spinning nozzle having perforations of about 125 to 250 t through a heated tube about 4meters long. During this treatment the solvent is substantially removed from the bundle of threads by means of a hot air current of about 180 C. traversing the tube.
In the wet spinning process, the bundle of threads is caused to issue from the nozzle, for example, into a bath of glycerine heated to about Bil-140 C.
The threads recovered in this process are particularly well adapted for being stretched up to twelve times their lengths. After having been shrunk again, they have a strength value of 38 Rkm. at about 20% elongation. Their resistivity against abrasion is about 6 times that of threads formed from the same material, however, without any addition as shown e. g. by the following tests.
One sample, in which no addition was made, had a geometric mean value of 65 abrasion tours.
Another sample also lacking any addition had a mean value of 80 abrasion tours.
A third sample of threads spun from a polyacrylonitrile solution to which had been added 16% polyvinylacetate and 8% polyvinylethylether had a mean value of 460 abrasion tours.
The expression abrasion tours points to the practice of pressing a rotating cylinder of Carborundum repeatedly against a thread and counting the number of revolutions before breakage.
The feel of the threads last soft and supple.
mentioned was particularly Example 2 17 kg. polyacrylonitrile having a K-value of about 90, 1.8 kg. polyvinylacetate having a K-value of about and 1.2 kg. polyvinylethylether having a K-value of about 50 were dissolved in kg. dimethylformamide and spun according to Example 1. After stretching there were obtained threads of great suppleness which had a breaking strength of up to 40 Rkm. at an elongation of 20-25%. These threads had a very soft feel.
Various changes may be made in the steps described in the foregoing specification without departing from the invention or sacrificing the advantages thereof.
I claim:
1. The method of improving the textile properties of threads of polyacrylonitrile type polymers, which comprises dissolving from 98 to 70 percent by weight of polyacrylonitrile, and from 2 to 30 percent by weight of a mixture in the proportion of from 2:1 to 1.5 :1, of polyvinylacetate and polyvinylethylether, in dimethylformamide, and spinning the solution thus obtained.
2. The method of improving the textile properties of threads of polyacrylonitrile type polymers, which comprises dissolving about percent by weight of polyacrylonitrile, and about 15 percent by weight of a mixture in the proportion of from about 2:1, of polyvinylacetate and polyvinylethylether, in dimethylformamide, and spinning the solution thus obtained.
References Cited in the file of this patent UNITED STATES PATENTS 2,123,599 Fikentscher et al July 12, 1938 2,404,714 Latham July 23, 1946 2,571,777 Stam'n et al. Oct. 16, 1951

Claims (1)

1. THE METHOD OF IMPROVING THE TEXTILE PROPERTIES OF THREADS OF POLYACRYLONTRILE TYPE POLYMERS, WHICH COMPRISES DISSOLVING FROM 98 TO 70 PERCENT BY WEIGHT OF POLYACRYLONTRILE, AND FROM 2 TO 30 PERCENT BY WEIGHT OF A MIXTURE IN THE PROPORTION OF FROM 2:1 TO 1.5:1, OF POLYVINYLACETATE AND POLYVINYLETHYLETHER, IN DIMETHYLFORMAMIDE, AND SPINNING THE SOLUTION THUS OBTAINED.
US466197A 1953-06-25 1954-11-01 Method of improving the textile properties of polyacrylonitrile threads Expired - Lifetime US2851435A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE326493X 1953-06-25
DEV6481A DE1004340B (en) 1953-06-25 1953-11-06 Process for the production of threads from polyacrylonitrile or its copolymers with improved textile properties

Publications (1)

Publication Number Publication Date
US2851435A true US2851435A (en) 1958-09-09

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 Before (1)

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

Country Status (7)

Country Link
US (2) US2833738A (en)
BE (2) BE528051A (en)
CH (3) CH326493A (en)
DE (1) DE1004340B (en)
FR (3) FR1230409A (en)
GB (3) GB752703A (en)
NL (1) NL83932C (en)

Cited By (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
US4438060A (en) 1979-11-28 1984-03-20 Bayer Aktiengesellschaft Process for producing cross-sectionally stable, hygroscopic fibers and filaments having a core-jacket structure
US4505870A (en) * 1982-07-06 1985-03-19 Bayer Aktiengesellschaft Preparation of low residual solvent content polyacrylonitrile filaments
US4508672A (en) * 1982-07-06 1985-04-02 Bayer Aktiengesellschaft Continuous dry-spinning process for highly shrinkable acrylonitrile filaments and fibers

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6323273B1 (en) 1995-05-22 2001-11-27 Cabot Corporation Elastomeric compounds incorporating silicon-treated carbon blacks

Citations (3)

* 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
US2404714A (en) * 1942-06-17 1946-07-23 Du Pont Polymer products
US2571777A (en) * 1950-04-08 1951-10-16 Eastman Kodak Co Acrylonitrile polymer mixed with copolymer of vinyl acetate and isopropenyl acetate

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2404725A (en) * 1944-11-18 1946-07-23 Du Pont Polymer solutions
US2571683A (en) * 1950-04-13 1951-10-16 Eastman Kodak Co Mixtures comprising polyacrylonitrile and a polyvinyl acetal
NL75895C (en) * 1950-04-26
US2620324A (en) * 1950-12-01 1952-12-02 Eastman Kodak Co Polymerization of acrylonitrile in the presence of amide polymers

Patent Citations (3)

* 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
US2404714A (en) * 1942-06-17 1946-07-23 Du Pont Polymer products
US2571777A (en) * 1950-04-08 1951-10-16 Eastman Kodak Co Acrylonitrile polymer mixed with copolymer of vinyl acetate and isopropenyl acetate

Cited By (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
US4438060A (en) 1979-11-28 1984-03-20 Bayer Aktiengesellschaft Process for producing cross-sectionally stable, hygroscopic fibers and filaments having a core-jacket structure
US4505870A (en) * 1982-07-06 1985-03-19 Bayer Aktiengesellschaft Preparation of low residual solvent content polyacrylonitrile filaments
US4508672A (en) * 1982-07-06 1985-04-02 Bayer Aktiengesellschaft Continuous dry-spinning process for highly shrinkable acrylonitrile filaments and fibers

Also Published As

Publication number Publication date
GB752703A (en) 1956-07-11
CH329999A (en) 1958-05-15
US2833738A (en) 1958-05-06
FR1100646A (en) 1955-09-22
DE1004340B (en) 1957-03-14
BE528051A (en)
FR66290E (en) 1956-06-28
NL83932C (en)
GB754775A (en) 1956-08-15
CH326494A (en) 1957-12-31
CH326493A (en) 1957-12-31
FR1230409A (en) 1960-09-15
GB752507A (en) 1956-07-11
BE528519A (en)

Similar Documents

Publication Publication Date Title
US2210774A (en) Fibers from ethylene polymers
Carothers et al. Studies of polymerization and ring formation. XV. Artificial fibers from synthetic linear condensation superpolymers
US2233442A (en) Polymeric vinylidene chloride article
ES488304A1 (en) Dry-spinning polymer filaments
CH313960A (en) Process for the production of tear-resistant fibers or threads from a synthetic polyester
ES313032A1 (en) Procedure for the preparation of filaments based on polyamide. (Machine-translation by Google Translate, not legally binding)
US2786043A (en) Plasticized acrylonitrile compositions
US3097415A (en) Acrylonitrile fiber and process for
US2851435A (en) Method of improving the textile properties of polyacrylonitrile threads
US2681265A (en) Spinning artificial filaments
US2822237A (en) Process for producing filament of vinyl chloride polymer
US3180845A (en) Method of preparing void free fibers from acrylonitrile polymers
US3342920A (en) Method of manufacturing synthetic fibers containing crystalline isotactic polystyrene having excellent physical properties
US2558793A (en) Mixtures comprising polyacrylonitrile and polyvinyl formate
EP0048846A2 (en) Fibres and filaments from acryl polymers that contain carboxyl groups, their use and process for their preparation
DE1435335C3 (en) Process for increasing the shrinkability of polyvinyl chloride fibers
DE1286684B (en) Process for the production of threads, fibers or films by wet or dry spinning of an acrylonitrile polymer mixture
DE763277C (en) Process for the production of threads from films of plastics
US3129273A (en) Process of producing non-fibrillating acrylonitrile polymer filaments
US2676161A (en) Compositions comprising a polymer of acrylonitrile and a cyanomethyl ester
US3122443A (en) Process for preventing cohesion between acrylonitrile polymer fibers with certain pentanediols
US3368015A (en) Spinning of acrylonitrile polymer solutions
US2631989A (en) Compositions comprising an acrylonitrile polymerization product and a dioxanone
US3701820A (en) Process for high speed wet spinning of acrylonitrile fibers
US2520150A (en) Compositions comprising an acrylonitrile polymerization product and an oxo-oxazolidine