US2617777A - Solutions of vinyl chloride polymer in a mixture of tetrahydrofurane and a solvent from the group consisting of sulfone, sulfoxides, sulfonic acid esters, and sulfinic acid esters - Google Patents

Solutions of vinyl chloride polymer in a mixture of tetrahydrofurane and a solvent from the group consisting of sulfone, sulfoxides, sulfonic acid esters, and sulfinic acid esters Download PDF

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US2617777A
US2617777A US221715A US22171551A US2617777A US 2617777 A US2617777 A US 2617777A US 221715 A US221715 A US 221715A US 22171551 A US22171551 A US 22171551A US 2617777 A US2617777 A US 2617777A
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solvent
acid esters
tetrahydrofurane
mixture
vinyl chloride
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US221715A
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Heisenberg Erwin
Kleine Johannes
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Glanzstoff AG
Vereinigte Glanzstoff Fabriken AG
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Glanzstoff AG
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    • 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
    • C08L27/00—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 a halogen; Compositions of derivatives of such polymers
    • C08L27/02—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 a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L27/04—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 a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
    • C08L27/06—Homopolymers or copolymers of vinyl chloride
    • 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
    • D01F6/08—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 halogenated hydrocarbons
    • D01F6/10—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 halogenated hydrocarbons from polyvinyl chloride or polyvinylidene chloride
    • 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
    • C08J2327/00—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 at least one being terminated by a halogen; Derivatives of such polymers
    • C08J2327/02—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 at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment
    • C08J2327/04—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 at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
    • C08J2327/06—Homopolymers or copolymers of vinyl chloride

Definitions

  • the present invention relates to liquid compositions of matter, more especially solutions of polymers and/or copolymers of vinyl chloride, which can be spun to form threads andthe like andwhich can be cast to form films.
  • the invention relates further to the production of such compositions and to the production of spun filaments with the aid thereof.
  • a primary object of the present invention is the embodiment of spinning solutions which are free of'the prior art defects as hereinbefore set forth.
  • a further object of the invention is the preparation of spun polymeric or copolymeric vinyl chloride filaments of improved physical properties and manifestly superior textile properties, and which can be further conditioned to produce superior textile fibers.
  • admixture with tetrahydrofurane according to the invention produces a fundamental change not only in the solvent power of dimethylsulfoxide but also in the solvent power of other solvents which have previously been proposed for polyacrylonitrile but which by themselves cannot be used to give vinyl chloride polymer solutions which can be satisfactorily spun.
  • Such compounds which can be used with tetrahydrofurane as solvents to give vinyl chloride polymer solutions which can be satisfactorily spun according to this invention comprise other sulfoxides and other chemical compounds of analogous structure, as for instance sulfones, sulfonic acid esters, sulfinic acid esters and the like, such for'example as:
  • the solvent mixture contains from to 50% by weight of the additional solvent.
  • the upper limit can be exceeded since even then a certain improvement in solubility is obtained.
  • solutions produced according to the invention can be spun without difliculty at room temperature to form artificial threads, artificial bristles and the like, either by the wet spinning process or by the dry spinning process. In this way for example artificial threads are obtained with a strength of 2.5 to 3 grams/ denier and extensions of l5-25%.
  • the solutions are also very suitable for the production of films by casting.
  • the solutions preferably contain from about to about by weight of polymer.
  • Example 1 200 parts by Weight of polyvinyl chloride are introduced with stirring at 20 C. into a mixture of 150 parts by weight of dimethylsulfoxide and 600 parts by weight of tetrahydrofurane. The mixture is heated slowly to boilin while stirring and, when complete solution has been achieved, it is cooled again to about 20 C. The resultant solution can be spun, for example through multihole stainless steel jets, into water at 20 C.
  • Example 2 150 parts by weight of polyvinyl chloride are introduced with stirring at 20 C. into a mixture of 100 parts by weight of dimethylsulfone and 600 parts by weight of tetrahydrofurane.
  • Example 3 150 parts by weight of a copolymer from equimolecular amounts of acrylonitrile and vinyl chloride are introduced with stirring at 20 C. into a mixture of parts by weight of dimethy-lsulfone and 600 parts by weight of tetrahydrofu-rane. The mixture is heated until complete solution takes place, and is then cooled again to room temperature whereupon, after filtering if necessary, it may be spun into filament form, for example into water at 25 C.
  • Example 5 parts by weight of polyvinyl chloride are introduced with stirring at 20 C. into a mixture of 60 parts by weight of dimethylsulfone and 600 parts by weight of tetrahydrofurane. The mixture is heated and, when complete solution has been achieved, is cooled again to room temperature. The solution is then ready for use in the spinning of threads or in the casting of films.
  • Example 6 150 parts by weight of polyvinyl chloride are introduced with stirring at 20 C.- into a mixture of 250 parts by weight of dimethylsulfoxide and 509 parts by Weight of tetrahydrofurane, and the mixture heated. After complete solution has taken place, the solution is cooled to 20 C. and filtered, if necessary. It may then be converted into spun thread or cast film form.
  • Example 7 The procedure described in Example 5 is repeated, using parts by weight of the polyvinyl chloride, 300 parts by weight of the dimethylsulfone, and 300 parts by weight of the tetrahydrofurane.
  • the obtained solution may be spun into water at 25 C. or may be cast into film form.
  • dimethylsulfone of Examples 4, 5 and '7 and the dimethylsulfoxide of Example 6 may, with equivalent results, be replaced by an equivalent amount of tetramethylenesulfoxide, hexamethylenesulfoxide or methane sulfinic acid methyl ester, while otherwise proceeding as described in the respective example.
  • a liquid composition of matter which can be spun to form threads and the like and which can be cast to form films comprising a vinyl chloride polymer as solute in solution in tetrahydrofurane as solvent, said solvent having admixed therewith from about 10 to about 50% by weight of the mixture, of an additional solvent selected from the group consisting of sulfone, sulfoxides, sulfonic acid esters and sulfinic acid esters which can di solve polyacrylonitrile completely but which do not by themselves give vinyl chloride polymer solutions which can be spun.
  • a liquid composition of matter which can be spun to form threads and the like and which can be cast to form films comprising a vinyl chloride polymer as solute in a solution in tetrahydrofurane as solvent, said solvent having admixed therewith from about 10 to about 50% by weight of the mixture, of a sulfoxide.
  • a liquid composition of matter which can be spun to form threads and the like and which can be cast to form films comprising a vinyl chloride polymer as solute in solution in tetrahydrofurane as solvent, said solvent having admixed therewith from about 10 to about 50% by weight of the mixture, of dimethylsulfoxide.
  • a liquid composition of matter which can be spun to form threads and the like and which can be cast to form films comprising a vinyl chloride polymer as solute in solution in tetrahydrofurane as solvent, said solvent having admixed therewith an additional solvent selected from the group consisting of sulfone, sulfoxides, sulfonic acid esters and sulfinic acid esters, the
  • a liquid composition of matter which can be spun to form threads and the like and which can be cast to form films comprising a vinyl chloride polymer as solute in solution in tetrahydrofurane as solvent, said solvent having admixed therewith dimethylsulfoxide, the proportion between dimethylsulfoxide and tetrahydrofurane in the solvent mixture being about 1:2 by weight.

Description

Patented Nov. 11, 1952 SOLUTIONS OF VINYL CHLORIDE POLYMER IN A MIXTURE OF TETRAHYDROFURANE AND A SOLVENT FROM THE GROUP CON- SISTING OF SULFONE, SULFOXIDES, SUL- ACID ESTERS, AND SULFINIC ACID E S Erwin Heisenberg, Erlenbach-on-the-Main, and Johannes Kleine, Munich, Germany, assignors to Vereinigte Glanzstoff-Fabriken A. G., Wup- I pertal-Elberfeld, Germany No Drawing. Application April 18, 1951, Serial No. 221,715. In Germany August 18, 1949 'The present invention relates to liquid compositions of matter, more especially solutions of polymers and/or copolymers of vinyl chloride, which can be spun to form threads andthe like andwhich can be cast to form films. The invention relates further to the production of such compositions and to the production of spun filaments with the aid thereof.
It has been proposed in the literature to dissolve polyvinyl chloride in tetrahydrofurane and to work up these solutions into artificial threads. In this way, however, solutions are obtained of gluey consistency which in practice cannot be spun.
Attempts have been made to overcome this disadvantage by subjecting the polyvinyl chloride to an additional chlorination before dissolving it. This does give an increased solubility, for example even in acetone, but such a procedure means that the process involves an additional step.
Even when the spinning properties are improved by heating the solutions before spinning, for example to 50 (3., and even when spinning is carried out at this temperature, a satisfactory result is not obtained. Moreover, when working in the vicinity of the boiling point of the solvent, bubbles are readily formed in the thread which considerably reduces its quality. The thread is also embrittled by spinning at raised temperature sothat optimum strength values are no longer obtained upon subsequent stretching.
A whole series of lactones and lactams have been proposed in the patent literature which are said to be suitable as solvents for high polymers and copolymers of vinyl compounds. Such solvents or mixtures thereof, however, do not give solutions which can be used to spin threads of high quality. 1
In order to increase the solubility of polyvinyl chloride, certain quantities of other vinyl compounds have been added during polymerization. It has in fact been possible to increase the solubility of polyvinyl chloride in this way, but only at the cost of imparting inferior textile properties to the spun threads prepared therefrom.
A primary object of the present invention is the embodiment of spinning solutions which are free of'the prior art defects as hereinbefore set forth. A further object of the invention is the preparation of spun polymeric or copolymeric vinyl chloride filaments of improved physical properties and manifestly superior textile properties, and which can be further conditioned to produce superior textile fibers. These objects are achieved ina simple way according to the present inven- 5 Claims. (Cl. 260-304) 2 tion, with production of good spinning solutions of vinyl chloride polymers and copolymers'from which high quality threads can be spun, by incorporating into the tetrahydrofurane, which is used as solvent, certain quantities of dimethylsulfoxide. The results thus achieved are surprising because neither tetrahydrofurane nor dimethylsulfoxide by itself gives vinyl chloride polymer solutions which can be satisfactorily spun. The favorable influence of dimethyl-sulfoxide becomes perceptible even on addition of about 10% by weight, relative to the weight of the solvent mixture, and increases with increasing quantity of the addition. The effect begins to diminish only when the dimethylsulfoxide becomes the predominant component of the mixture. A particularly favorable proportion of the two said compounds in the mixture is a proportion of one part by weight of dimethylsulfoxide to two parts by weight of tetrahydrofurane.
Moreover, admixture with tetrahydrofurane according to the invention produces a fundamental change not only in the solvent power of dimethylsulfoxide but also in the solvent power of other solvents which have previously been proposed for polyacrylonitrile but which by themselves cannot be used to give vinyl chloride polymer solutions which can be satisfactorily spun. Such compounds which can be used with tetrahydrofurane as solvents to give vinyl chloride polymer solutions which can be satisfactorily spun according to this invention comprise other sulfoxides and other chemical compounds of analogous structure, as for instance sulfones, sulfonic acid esters, sulfinic acid esters and the like, such for'example as:
Tetramethylenesulfoxide Pentamethylenesulfoxide Hexamethylenesulfoxide; a-Methyl-trimethylenesulfoxide; 'I'rimethylenesulfoxide; a-Methyl -tetramethylene-sulfoxi-de; fl-Methyl-tetramethylene-sulfoxide p-Keto-tetramethylene -sulfoxide Methane sulfonic acid methyl ester; Methane sulfonic acid ethyl ester; Methane disulf-onic acid dimethyl ester; Methane disulfonic acid diethyl est-er; Ethane-1,2-disulfonic acid diethyl ester; Ethane-LZ-disulfonic acid dimethyl ester; Butane-1,4-disulf-oni-c acid dimethyl ester; Propane-1,3-disulfonic acid dimethyl ester; Chloromethane-disulfonic acid dimethyl ester; Ethane sulfinic acid methyl ester;
Methane sulfinic acid ethyl ester;
3 Methane sulfinio acid methyl ester; Dimethylsulfone; p-Hydroxyethyl-methylsulfone; Tetramethylenesulfone B-Methoxy-tetramethylenesulfone a-Methoxy-tetramethylenesulfone; a-Methyl-tetramethylenesulfone; B-Methyl-tetramethylenesulfone; B-Hydroxy-tetramethylenesulfone; a-Methyl-pentamethylenesulfone Hex amethylenes ulfone p-Amino-tetramethylenesulfone ,B-Keto-tetramethylenesulfone;
- 13-Bromo-tetramethylenesultone;
a-Methyl-trimethylenesulfone; Pentamethylenesulfone Trimethylenesulfone; a.-Cyanomethyl-trimethylenesulfone; etc.
Preferably the solvent mixture contains from to 50% by weight of the additional solvent. In certain circumstances the upper limit can be exceeded since even then a certain improvement in solubility is obtained.
The examples given below describe in more detail individual mixtures which have particularly good properties due to the nature and proportions of their ingredients.
When more than one of the said additional substances are admixed with tetrahydrofurane, which is possible according to the present invention, preferably the proportions of the ingredients are maintained within the above described limits, the total quantity of the additional substances lying within these limits.
The favorable effects in improvin the solubility with the solvent mixtures used according to the invention are obtained not only with polyvinyl chloride but also with copolymers of vinyl chloride, for example vinyl chloride-vinyl acetate copolymers, vinyl chIoride-vinylidene chloride copolymers, vinyl chloride-styrene copolymers, vinyl chloride-vinyl acetate-vinylidene chloride copo-lymer-s, etc.
One of the most important advantages of solutions produced according to the invention is that the solutions can be spun without difliculty at room temperature to form artificial threads, artificial bristles and the like, either by the wet spinning process or by the dry spinning process. In this way for example artificial threads are obtained with a strength of 2.5 to 3 grams/ denier and extensions of l5-25%. The solutions are also very suitable for the production of films by casting. The solutions preferably contain from about to about by weight of polymer.
The following examples describe, solely by way of illustration, presently preferred embodiments of the process of the invention.
Example 1 200 parts by Weight of polyvinyl chloride are introduced with stirring at 20 C. into a mixture of 150 parts by weight of dimethylsulfoxide and 600 parts by weight of tetrahydrofurane. The mixture is heated slowly to boilin while stirring and, when complete solution has been achieved, it is cooled again to about 20 C. The resultant solution can be spun, for example through multihole stainless steel jets, into water at 20 C.
Example 2 150 parts by weight of polyvinyl chloride are introduced with stirring at 20 C. into a mixture of 100 parts by weight of dimethylsulfone and 600 parts by weight of tetrahydrofurane. The
4 mixture is heated slowly to boiling while stirring and, when complete solution has been achieved, it is cooled again to about 20 C. The resultant solution can be spun into water at 20 C.
Example 3 Example 4 150 parts by weight of a copolymer from equimolecular amounts of acrylonitrile and vinyl chloride are introduced with stirring at 20 C. into a mixture of parts by weight of dimethy-lsulfone and 600 parts by weight of tetrahydrofu-rane. The mixture is heated until complete solution takes place, and is then cooled again to room temperature whereupon, after filtering if necessary, it may be spun into filament form, for example into water at 25 C.
Example 5 .parts by weight of polyvinyl chloride are introduced with stirring at 20 C. into a mixture of 60 parts by weight of dimethylsulfone and 600 parts by weight of tetrahydrofurane. The mixture is heated and, when complete solution has been achieved, is cooled again to room temperature. The solution is then ready for use in the spinning of threads or in the casting of films.
Example 6 150 parts by weight of polyvinyl chloride are introduced with stirring at 20 C.- into a mixture of 250 parts by weight of dimethylsulfoxide and 509 parts by Weight of tetrahydrofurane, and the mixture heated. After complete solution has taken place, the solution is cooled to 20 C. and filtered, if necessary. It may then be converted into spun thread or cast film form.
Example 7 The procedure described in Example 5 is repeated, using parts by weight of the polyvinyl chloride, 300 parts by weight of the dimethylsulfone, and 300 parts by weight of the tetrahydrofurane. The obtained solution may be spun into water at 25 C. or may be cast into film form.
The dimethylsulfone of Examples 4, 5 and '7 and the dimethylsulfoxide of Example 6 may, with equivalent results, be replaced by an equivalent amount of tetramethylenesulfoxide, hexamethylenesulfoxide or methane sulfinic acid methyl ester, while otherwise proceeding as described in the respective example.
Having thus disclosed the invention, what is claimed is I l. A liquid composition of matter which can be spun to form threads and the like and which can be cast to form films, comprising a vinyl chloride polymer as solute in solution in tetrahydrofurane as solvent, said solvent having admixed therewith from about 10 to about 50% by weight of the mixture, of an additional solvent selected from the group consisting of sulfone, sulfoxides, sulfonic acid esters and sulfinic acid esters which can di solve polyacrylonitrile completely but which do not by themselves give vinyl chloride polymer solutions which can be spun.
2. A liquid composition of matter which can be spun to form threads and the like and which can be cast to form films, comprising a vinyl chloride polymer as solute in a solution in tetrahydrofurane as solvent, said solvent having admixed therewith from about 10 to about 50% by weight of the mixture, of a sulfoxide.
3. A liquid composition of matter which can be spun to form threads and the like and which can be cast to form films, comprising a vinyl chloride polymer as solute in solution in tetrahydrofurane as solvent, said solvent having admixed therewith from about 10 to about 50% by weight of the mixture, of dimethylsulfoxide.
4. A liquid composition of matter which can be spun to form threads and the like and which can be cast to form films, comprising a vinyl chloride polymer as solute in solution in tetrahydrofurane as solvent, said solvent having admixed therewith an additional solvent selected from the group consisting of sulfone, sulfoxides, sulfonic acid esters and sulfinic acid esters, the
proportion between additional solvent and tetrahydrofurane in the solvent mixture being about 1:2 by weight.
5. A liquid composition of matter which can be spun to form threads and the like and which can be cast to form films, comprising a vinyl chloride polymer as solute in solution in tetrahydrofurane as solvent, said solvent having admixed therewith dimethylsulfoxide, the proportion between dimethylsulfoxide and tetrahydrofurane in the solvent mixture being about 1:2 by weight.
ERWIN HEISENBERG. JOHANNES KLEINE.
Number Name Date Stuchlik Mar. 13, 1951

Claims (1)

1. A LIQUID COMPOSITION OF MATTER WHICH CAN BE SPUN TO FORM THREADS AND THE LIKE AND WHICH CAN BE CAST TO FORM FILMS, COMPRISING A VINYL CHLORIDE POLYMER AS SOLUTE IN SOLUTION IN TETRAHYDROFURANE AS SOLVENT, SAID SOLVENT HAVING ADMIXED THEREWITH FROM ABOUT 10 TO ABOUT 50% BY WEIGHT OF THE MIXTURE, OF AN ADDITIONAL SOLVENT SELECTED FROM THE GROUP CONSISTING OF SULFONE, SULFOXIDES, SULFONIC ACID ESTERS AND SULFINIC ACID ESTERS WHICH CAN DISSOLVE POLYACRYLONITRILE COMPLETELY BUT WHICH DO NOT BY THEMSELVES GIVE VINYL CHLORIDE
US221715A 1949-08-18 1951-04-18 Solutions of vinyl chloride polymer in a mixture of tetrahydrofurane and a solvent from the group consisting of sulfone, sulfoxides, sulfonic acid esters, and sulfinic acid esters Expired - Lifetime US2617777A (en)

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US221713A Expired - Lifetime US2616868A (en) 1949-08-18 1951-04-18 Spinning solutions of vinyl chloride polymer dissolved in a solvent mixture containing tetrahydrofurane and an additional solvent selected from the group consisting of lactones and lactams
US221715A Expired - Lifetime US2617777A (en) 1949-08-18 1951-04-18 Solutions of vinyl chloride polymer in a mixture of tetrahydrofurane and a solvent from the group consisting of sulfone, sulfoxides, sulfonic acid esters, and sulfinic acid esters

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US221713A Expired - Lifetime US2616868A (en) 1949-08-18 1951-04-18 Spinning solutions of vinyl chloride polymer dissolved in a solvent mixture containing tetrahydrofurane and an additional solvent selected from the group consisting of lactones and lactams

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DE965657C (en) * 1953-08-28 1957-06-13 Basf Ag Solvent for acetylene
US3005739A (en) * 1957-04-29 1961-10-24 Donald D Lang Method and apparatus for making multiconductor cable
US3109828A (en) * 1959-12-30 1963-11-05 Mobil Finishes Company Inc Dimethyl sulfoxide-aromatic hydrocarbon solvent system for vinyl chloride copolymers
US3361697A (en) * 1965-03-24 1968-01-02 Du Pont Plasticized polylactams containing cyclic saturated sulfone
US4454091A (en) * 1980-06-10 1984-06-12 Rhone-Poulenc-Textile Solutions, which can be shaped, from mixtures of cellulose and polyvinyl chloride, and shaped articles resulting therefrom and the process for their manufacture
CN102414173A (en) * 2009-05-04 2012-04-11 罗地亚经营管理公司 Method for preparing fluoroalkanesulphinic acid esters
US20180016416A1 (en) * 2015-03-31 2018-01-18 Kaneka Corporation Thermoplastic modacrylic resin composition, method for manufacturing same, molded article of same, and acrylic fibers and method for manufacturing same

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US2756218A (en) * 1953-10-09 1956-07-24 Chemstrand Corp Solutions of acrylonitrile polymers in 1, 5-dimethylpyrrolidone-2
US2906721A (en) * 1956-09-28 1959-09-29 Dow Chemical Co Method for preparing tetrahydrofuran lacquer of wet vinylidene chlorideacrylonitrile copolymer
US2918443A (en) * 1957-01-31 1959-12-22 American Marietta Co Vinyl chloride-vinyl acetate copolymer dissolved in solvent mixture containing aromatic hydrocarbon and pyrrolidone component
US2913430A (en) * 1957-04-09 1959-11-17 American Marietta Co Vinyl chloride-vinyl acetate copolymer dissolved in solvent mixture containing aromatic hydrocarbon and lactone component
GB1035998A (en) * 1962-07-28 1966-07-13 Kurashiki Rayon Kk Method of manufacturing a spinning solution
DK153684C (en) * 1982-12-01 1990-02-26 Heimann F & Co As PROCEDURE FOR PREPARING A LIMITED JOINT BETWEEN SURFACES OF SUBSTANCES MADE BY WATER INSOLuble, SYNTHETIC ORGANIC POLYMERS
US4767808A (en) * 1984-10-05 1988-08-30 Hercon Laboratories Corporation Article useful for administration of pharmacologically-active substances transdermally, orally, or by means of implant
US4687798A (en) * 1986-01-27 1987-08-18 King Lloyd H Sr Solvent cement
FR2638167B1 (en) * 1988-10-26 1994-07-29 Eternit Financiere ADHESIVE FOR PLASTIC MATERIALS AND METHOD OF IMPLEMENTING THE SAME
US5821289A (en) * 1996-07-19 1998-10-13 The B.F. Goodrich Company Low volatile organic solvent based adhesive
US5817708A (en) * 1996-07-19 1998-10-06 The B. F. Goodrich Company Low volatile organic solvent based adhesive

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Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE965657C (en) * 1953-08-28 1957-06-13 Basf Ag Solvent for acetylene
US3005739A (en) * 1957-04-29 1961-10-24 Donald D Lang Method and apparatus for making multiconductor cable
US3109828A (en) * 1959-12-30 1963-11-05 Mobil Finishes Company Inc Dimethyl sulfoxide-aromatic hydrocarbon solvent system for vinyl chloride copolymers
US3361697A (en) * 1965-03-24 1968-01-02 Du Pont Plasticized polylactams containing cyclic saturated sulfone
US4454091A (en) * 1980-06-10 1984-06-12 Rhone-Poulenc-Textile Solutions, which can be shaped, from mixtures of cellulose and polyvinyl chloride, and shaped articles resulting therefrom and the process for their manufacture
CN102414173A (en) * 2009-05-04 2012-04-11 罗地亚经营管理公司 Method for preparing fluoroalkanesulphinic acid esters
CN102414173B (en) * 2009-05-04 2014-01-01 罗地亚经营管理公司 Method for preparing fluoroalkanesulphinic acid esters
US20180016416A1 (en) * 2015-03-31 2018-01-18 Kaneka Corporation Thermoplastic modacrylic resin composition, method for manufacturing same, molded article of same, and acrylic fibers and method for manufacturing same
US20190300675A1 (en) * 2015-03-31 2019-10-03 Kaneka Corporation Thermoplastic modacrylic resin composition, method for manufacturing same, molded article of same, and acrylic fibers and method for manufacturing same
US10752752B2 (en) * 2015-03-31 2020-08-25 Kaneka Corporation Thermoplastic modacrylic resin composition, method for manufacturing same, molded article of same, and acrylic fibers and method for manufacturing same
US10787558B2 (en) * 2015-03-31 2020-09-29 Kaneka Corporation Thermoplastic modacrylic resin composition, method for manufacturing same, molded article of same, and acrylic fibers and method for manufacturing same

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US2616868A (en) 1952-11-04
FR1023581A (en) 1953-03-20

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