US3009894A - Spinning solution comprising acrylonitrile polymer in glycolic acid nitrile and ethylene chlorohydrin, and process for making - Google Patents

Spinning solution comprising acrylonitrile polymer in glycolic acid nitrile and ethylene chlorohydrin, and process for making Download PDF

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Publication number
US3009894A
US3009894A US596152A US59615256A US3009894A US 3009894 A US3009894 A US 3009894A US 596152 A US596152 A US 596152A US 59615256 A US59615256 A US 59615256A US 3009894 A US3009894 A US 3009894A
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US
United States
Prior art keywords
weight
glycolic acid
spinning
acid nitrile
polyacrylonitrile
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Expired - Lifetime
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US596152A
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English (en)
Inventor
Pirot Ernst
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Glanzstoff AG
Vereinigte Glanzstoff Fabriken AG
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Glanzstoff AG
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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
    • 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

Definitions

  • This invention relates to a novel solvent for poly acrylonitrile and mixed polymers of polyacrylonitrile.
  • the invention further relates to a spinning solution and improved process for spinning artificial filaments, and more particularly for spinning filaments, threads, fibers or the like, of polyacrylonitrile or mixed polymers of polyacrylonitrile from a spinning solution containing the polymer dissolved therein.
  • glycolic acid nitrile solvent The addition of nitromethane or aliphatic diesters to the glycolic acid nitrile solvent has been attempted but does not provide any substantial improvement in the properties of the spinning solution as regards its stability against decomposition and its tendency toward stickiness. Also, if glycolic acid nitrile is used alone as the solvent for polyacrylonitrile, it is particularly diflicult to favorably and satisfactorily develop the thread or filament in a subsequent wet-spinning process.
  • One object of the present invention is to provide a novel and effective solvent for poly'aorylonitrile and mixed polymeers of polyacrylonitrile.
  • Another object of the invention is to provide a novel spinning solution for spinning artificial filaments of polyacrylonitrile or its mixed polymers.
  • Still another object of the invention is to provide an improved process for spinning artificial filaments of polyacrylonitrile or its mixed polymers.
  • Yet another object of the invention is to provide a solvent for the purpose described whereby the disadvantages of stickiness or tackiness can be avoided.
  • Another object of the invention is to provide a solvent or spinning solution which is stable against decomposition.
  • Another object of the invention is to provide artificial filaments of polyacrylonitrile or its mixed polymers which have improved textile or fiber properties and characteristics, including an especially good color stability.
  • Glycolic acid nitrile is a well known and readily obtainable solvent, sometimes named methylene cyanohydrin, formaldehyde cyanohydrin, or hydroxy methyl cyanide.
  • Ethlyene chlorohydrin is likewise readily obtainable under various other names such as chloroethyl alcohol, 2-chloroethyl alcohol, and l-hydroxy-Z-chloroethane.
  • Glycolic acid nitrile can be prepared from formalin (-40%) to which there are added equimolecular quantities of hydrocyanic acid (see Beilsteins Handbuch de Organischen Chemie, 4th edition,
  • the solvent mixture preferably consists of these two compounds or components in proportions of about 60 to 95% by Weight of glycolic acid nitrile and about 405% by weight of ethylene chlorohydrin.
  • the most effective proportion is obtained in a mixture preferably containing about 35 to 25% by weight of ethylene chlorohydrin and a corresponding proportion of about 65 to by weight of glycolic acid nitrile.
  • a solvent-reducing substance i.e., a suitable reducing agent
  • a solvent-reducing substance i.e., a suitable reducing agent
  • a suitable reducing agent such as sulfur dioxide or a formaldehyde
  • the quantity of reducing agent required is less than 1% by weight of the solvent mixture, the exact quantity being readily determined by routine experimentation.
  • Tht solvent mixture or spinning solution to which such a reducing agent has been added and the threads spun from the solution are distinguished by a very bright color which fails to darken even after a considerable period of heating.
  • suitable reducing agents include paraformald-ehyde, hydroxylamine, alkali metal-hydrosulfite, rongalite.
  • the novel glycolic acid nitrile-ethylene chlorohydrin solvent is particularly adapted to the formation of spinning solutions of polyacrylonitrile.
  • the solvent is also eifectively utilized with a modified polyacrylonitrile such as is obtained by a copolymerization with various other monomeric compounds such as methyl methacrylate, acrylic acid amides, methacrylate, vinyl pyridine, and vinyl carbazole.
  • Such copolymerization results in mixed polymers or hetero-polymers of polyacrylonitrile which have about the same characteristics as polyacrylonitrile itself, particularly where the acrylonitrile monomer forms a major proportion of the mixed polymer.
  • the solvent and spinning solution of the invention is preferably applicable to those mixed polymers of acrylonitrile in which the proportion of acrylonitrile is at least by weight.
  • the use of the solvent mixture of the invention provides a spinning solution of polyacrylonitrile or its mixed polymers which neither tends to become sticky or tacky nor shows signs of decomposition.
  • the spinning of polyacrylonitrile proceeds more perfectly than has heretofore been possible.
  • the threads or spun filaments can be finished either by the dry-spinning process or by 0 the wet-spinning process, and the finished thread is well developed with uniform physical and chemical properties, particularly for use in the textile industry.
  • Example 1 1.8 kilograms of polyacrylonitrile (K value about 95) and 8.2 kilograms of a solvent mixture consisting of 70% by weight of glycolic acid nitrile and 30% by weight of ethylene chlorohydrin are mixed together at a temperature of about 15 C. to 20 C. The resulting solution is concurrently deaerated. The fully deaerated mixture, while being constantly stirred, is gradually brought to a temperature of about 110 C. to 115 C. and kept at this temperature for approximately one hour. A very brilliant spinning solution forms which is then filtered and spun by the dry-spinning process. The resulting threads after being stretched 1000% have a strength of 4.4 grams per denier with an elongation at break of 11 to 12%. After the co-called thermo-fixing of the stretched or drawn threads, the strength increases to from 4.8 to 5.0 grams per denier and the elongation at break rises to from 20 to 25%.
  • Example 2 A spinning solution is formed as described in Example 1, except, however, that sulfur dioxide is introduced into the solvent mixture before the formation of the spinning solution. Sufiicient sulfur dioxide is introduced to give a pH value of about 3.
  • the spinning solution is now spun through a multiple-hole nozzle or spinneret at approximately room temperature into a precipitating bath 4 meters in length which is filled with 80% technical xylol and 20% butanol.
  • the spinning speed or drawing off of the threads is about 70 meters per minute.
  • the resulting bundle of thread is squeezed through a mangle, wound in the customary manner, and then stretched or drawn. With a 900% stretch and subsequent thermo-fixing at 125 C. for a period of 30 minutes, the thread has a strength of approximately 4.7 grams per denier with an elongation at break of 22 to 25%.
  • Example 3 1.6 kilograms of a modified polyacrylonitrile (K value about 100), which is formed by copolymerizing 94% of acrylonitrile and 6% methyl methacrylate, are dissolved at 110 C. to 115 C. corresponding to the data in Example l, with 8.4 kilograms of a solvent mixture consisting of 65% by weight of glycolic acid nitrile and 35% by weight of ethylene chlorohydrin, 0.5% of paraformaldehyde being added (with reference to the quantity of the solvent mixture). The solution is filtered and spun as in Example 2. After stretching and thermo-fixing, threads are obtained which are well adapted to dyeing and which have a very soft handle.
  • K value about 100 a modified polyacrylonitrile
  • a solution for spinning artificial filaments comprising a polymer of the group consisting of polyacrylonitrile and copolymers of acrylonitrile containing at least 85% by weight of acrylonitrile and another monomer selected from the group consisting of methyl methacrylate, acrylic acid amides, methyl acrylate, vinyl pyridine and vinyl carbazole dissolved in a mixture of about 60 to 95 per cent by weight of glycolic acid nitrile and about 40 to percent by weight of ethylene chlorohydrin.
  • a solution for spinning artificial filaments comprising a polymer of the group consisting of polyacrylonitrile and copolymers of acrylonitrile containing at least 85% by weight of acrylonitrile and another monomer selected from the group consisting of methyl methacrylate, acrylic acid amides, methyl acrylate, vinyl pyridine and vinyl carbazole dissolved in a mixture of about 60 to 95 percent by weight of glycolic acid nitrile and about 40 to 5 percent by weight of ethylene chlorohydrin, said mixture also containing less than about 1% by weight of a reducing agent.
  • a solution for spinning artificial filaments comprising polyacrylonitrile dissolved in a mixture of about 60 to 95 percent by weight of glycolic acid nitrile and about 40 to 5 percent by weight of ethylene chlorohydrin, said mixture also containing less than about 1% by weight of sulfur dioxide.
  • a solution for spinning artificial filaments comprising a copolymer of acrylonitrile and methyl methacrylate dissolved in a mixture of about 60 to 95 percent by weight of glycolic acid nitrile and about 40 to 5 percent by weight of ethylene chlorohydrin, said mixture also containing less than about 1% by weight of said solution of paraformaldehyde.
  • a solution for spinning artificial filaments comprising a polymer of the group consisting of polyacrylonitrile and copolymers of acrylonitrile containing at least 85% by Weight of acrylonitrile and another monomer selected from the group consisting of methyl methacrylate, acrylic acid amides, methyl acrylate, vinyl pyridine and vinyl carbazole dissolved in a mixture of about 65 to 75 percent by weight of glycolic acid nitrile and about 35 to 25 percent by weight of ethylene chlorohydrin.
  • a solution for spinning artificial filaments as claimed in claim 9 containing less than about 1% by weight of a reducing agent.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Toxicology (AREA)
  • Dispersion Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Artificial Filaments (AREA)
US596152A 1955-07-08 1956-07-06 Spinning solution comprising acrylonitrile polymer in glycolic acid nitrile and ethylene chlorohydrin, and process for making Expired - Lifetime US3009894A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEV9168A DE1007945B (de) 1955-07-08 1955-07-08 Verfahren zur Herstellung von Spinnloesungen aus Polyacrylnitril bzw. seinen Mischpolymerisaten

Publications (1)

Publication Number Publication Date
US3009894A true US3009894A (en) 1961-11-21

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US (1) US3009894A (enrdf_load_stackoverflow)
BE (1) BE548806A (enrdf_load_stackoverflow)
CH (1) CH345110A (enrdf_load_stackoverflow)
DE (1) DE1007945B (enrdf_load_stackoverflow)
FR (1) FR1151623A (enrdf_load_stackoverflow)
GB (1) GB794396A (enrdf_load_stackoverflow)
NL (2) NL207832A (enrdf_load_stackoverflow)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1282932B (de) * 1962-08-07 1968-11-14 Bayer Ag Verfahren zur Herstellung von Loesungen aus Acrylnitrilpolymerisaten in organischen Loesungsmitteln

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB694827A (en) * 1948-10-02 1953-07-29 Roehm & Haas Gmbh Improvements in or relating to the treatment of polymerides and mixed polymerides ofacrylonitrile
US2843558A (en) * 1953-06-08 1958-07-15 Asahi Chemical Ind Compositions comprising acrylonitrile polymers and diamides

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE891018C (de) * 1949-12-18 1953-09-24 Roehm & Haas G M B H Loesungsmittel fuer Polyacrylnitrile und deren Mischpolymerisate mit ueberwiegendem Acrylnitrilgehalt

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB694827A (en) * 1948-10-02 1953-07-29 Roehm & Haas Gmbh Improvements in or relating to the treatment of polymerides and mixed polymerides ofacrylonitrile
US2843558A (en) * 1953-06-08 1958-07-15 Asahi Chemical Ind Compositions comprising acrylonitrile polymers and diamides

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Publication number Publication date
DE1007945B (de) 1957-05-09
CH345110A (de) 1960-03-15
NL90746C (enrdf_load_stackoverflow)
FR1151623A (fr) 1958-02-03
GB794396A (en) 1958-04-30
NL207832A (enrdf_load_stackoverflow)
BE548806A (enrdf_load_stackoverflow)

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