US3066008A - Process for producing fibers from copolymers of acrylonitrile and vinylidene chloride - Google Patents

Process for producing fibers from copolymers of acrylonitrile and vinylidene chloride Download PDF

Info

Publication number
US3066008A
US3066008A US10880A US1088060A US3066008A US 3066008 A US3066008 A US 3066008A US 10880 A US10880 A US 10880A US 1088060 A US1088060 A US 1088060A US 3066008 A US3066008 A US 3066008A
Authority
US
United States
Prior art keywords
fibres
percent
stretching
acrylonitrile
fibers
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
US10880A
Inventor
Carpenter Albert Stanley
Timms Richard Neville
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.)
Akzo Nobel UK PLC
Original Assignee
Courtaulds PLC
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 Courtaulds PLC filed Critical Courtaulds PLC
Application granted granted Critical
Publication of US3066008A publication Critical patent/US3066008A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

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
    • D01F6/28Monocomponent 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
    • 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
    • D01F6/32Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds comprising halogenated hydrocarbons as the major constituent

Definitions

  • This invention relates to the manufacture of synthetic fibres and is particularly concerned with the manufacture of fibres from the copolymers of acrylonitrile and vinylidene chloride which are soluble in acetone.
  • the invention is applicable to acetone-soluble binary copolymers of acrylonitrile and vinylidene chloride and also acetonesoluble copolymers of the two compounds with small amounts, for example up to about percent by weight, of other monomers such as vinyl pyridine or itaconic acid which may be used to modify the dyeing properties of the copolymer.
  • acetonesoluble copolymers of acrylonitrile and vinylidene chloride see for example British patent specification No. 643,198 and the Carpenter application Serial No. 788,045, now Patent No. 3,004,008.
  • the acetone solutions of the copolymers may be wet or dry spun to form fibres as described for example in British patent specification No. 674,323 of British Celanese Limited.
  • This latter specification also describes the step of stretching the resultant fibres in a heat-softened condition, for example in a hot water bath or in saturated steam; the stretching step may be followed by an annealing treatment so as to reduce the tendency of the fibres to shrink when heated to moderately elevated temperatures such as 60 to 100. C.
  • the term cold stretching means that the fibres are stretched at a temperature not greater than C. In general, for economic reasons, the fibres are stretched at the ordinary temperatures.
  • the degree of stretching should be at least 75 percent and may conveniently be from 100 to 300 percent. Throughout this specification the degree of stretching is expressed as the percentage of the increased length on the original length of the fibre; for example for a fibre stretched to twice its original length the stretch is 100 percent.
  • the cold stretching of the freshly extruded fibres is preferably effected between godets, the fibres leaving the spinning cell or the coagulating bath, as the case may be, being passed round a first godet and then to a second godet the peripheral speed of which is arranged to give the fibres the required degree of stretching.
  • godets the fibres leaving the spinning cell or the coagulating bath, as the case may be, being passed round a first godet and then to a second godet the peripheral speed of which is arranged to give the fibres the required degree of stretching.
  • other known methods of stretching for example using reels or rollers, or a combination of a godet and reel, may be used.
  • the cold stretching is preferably elfected in air, particularly when dry spun fibres are being stretched, but stretching may be effected in water or other non-solvent estates Patented Nov. 27, 1962 at 15-40 C., and the liquid may contain a textile lubricant.
  • One efiect of the cold stretching operation is to make the fibres less rubbery in character.
  • a second eifect is to reduce appreciably or to eliminate entirely the risk of stuck filaments in the collected yarn.
  • the fibres produced by the cold stretching operation are not however suitable for general textile uses and they are therefore given a further stretch treatment at elevated temperature.
  • Such further stretching should be from 500 to 2,000 percent and preferably 700 to 1,500 percent.
  • Suitable elevated temperatures are temperatures not less than C.
  • Such hot stretching may be carried out in hot air, steam or hot water under pressure as described in the above mentioned British specification No. 674,323 and United States Patent No. 2,679,450, and the hot stretching process may be followed by an annealing treatment to reduce the shrinkage of the fibre on heating.
  • the hot stretching treatment is carried out at temperatures above C. using saturated steam at superatmospheric pressure, for example up to 50 lbs. per square inch, as the heating medium.
  • the fibres obtained as a result of stretching the cold-stretched fibres in saturated steam at superatmospheric pressure have high dimensional stabilities to wet and dry heat which are adequate for many textile purposes.
  • the fibres so stretched contract only a few percent in boiling water or in air at 136 C. and, moreover, a marked improvement in colour stability on exposure to dry heat is also obtained.
  • still further stabilization can be effected by an annealing treatment carried out by immersing the fibres in hot or boiling water, in open steam, in steam under pressure or in hot air while allowing the natural contraction of the fibre to take place freely.
  • the fibres after the stretching treatment in saturated steam at superatmospheric pressure, may be passed continuously, under conditions of free relaxation, through a bath of water at, or near, its boiling point (that is to say at about 90-100 C.), or through a tube containing saturated steam at atmospheric pressure.
  • the resulting fibres show virtually no contraction on subsequent immersion in boiling water.
  • the present invention is illustrated by the accompanying drawings.
  • the acetone solution of the acrylonitrilevinylidene chloride copolymer is extruded through a jet 1 within a spinning cell 2 to form filaments 3; hot air is continuously circulated within the cell 2 in known manner.
  • the filaments 3 leaving the cell 2 are lapped round a godet 4 and are passed directly to a second godet 5 moving at 'a peripheral speed designed to stretch the filaments at least 75 percent in air between the two godets. From the godet 5 the filaments 3 are collected, without twist, on a bobbin 6.
  • the cold stretched filaments are hot stretched.
  • the filaments 3 are withdrawn from the bobbin 6 and lapped round a godet 7 before being drawn through a steam chest 8 by a godet 9 which stretches the filament in contact with the steam at least 500 percent.
  • the hot stretched filaments are then passed by way of guides 10,.
  • Example 1 amide solution was dissolved in acetone to give a 22 percent by weight solution. This solution was dry spun on conventional dry spinning equipment and the resulting fibres leaving the spinning cell were cold stretched 100 percent between godets and were then collected, untwisted, on a bobbin. The final collection speed was 40 metres per minute and the denier was 266. Examination of the collected yarn showed no stuck filaments and the yarn could be removed from the bobbin without difficulty, even after prolonged storage.
  • the yarn was then withdrawn from the bobbin and passed continuously, with stretching, through saturated steam at 30 lbs. per square inch using an apparatus consisting of two adjoining chambers, containing respectively hot water under pressure and then steam under pressure, and was finally collected as a twisted yarn.
  • the yarn was passed into the water through a plate containing a fine orifice, and from the water into the steam through a second orifice and out of the steam through a third orifice.
  • the stretching tension was 2 grams.
  • the denier of the collected yarn was 26, its tenacity was 4.35 grams denier, its extensibility was 10.7 percent and its contraction on immersion in boiling water for seconds was 4.6 percent.
  • the cold-stretched yarn before the hot stretching process had a tenacity of 1.47 grams/denier, an extensibility of 53.8 percent and a contraction in boiling water of 37 percent.
  • the yarn was finally passed continuously through a bath of boiling water under conditions of free relaxation, the immersion time being 11 seconds. Its tenacity was then 3.40, grams/ denier, its extensibility 13.8 percent and its contraction in boiling water about 0.5 percent; it
  • Example 2 A copolymer of acrylonitrile and vinylidene chloride was produced by the method described in the Carpenter application Serial No. 788,045, now Patent No. 3,004,008, the copolymer containing 47 percent by weight of acrylonitrile and having an intrinsic viscosity, measured in dimethyl formamide, of 1.73. It was dissolved in acetone to produce a 22 percent by weight solution which was then dry spun through a 40 hole jet as described in Example l to produce fibres which Were stretched 100 percent at ordinary temperatures between a godet and a thread-advancing reel and then collected on bobbins without twist. The collected yarn was 900 denier/ 40 filament yarn.
  • the yarn was withdrawn from the bobbin by a godet having a peripheral speed of 4 metres/minute and stretched 1,150 percent in saturated steam at lbs. per
  • the yarn obtained had a tenacity of 4 grams/denier and an extensibility of 14 percent. It was dimensionally stable to dry and wet heat. It was woven into a fabric which was found to be flame-proof according to the British standards specification. Samples of the fabric were unaffected by contact for 5 seconds with a hot iron at temperatures up to 220 C.
  • thermoforming the hotstretched fibres are subjected to an annealing treatment in which they are heated while allowing the natural contraction of the fibres to take place freely.

Description

Nov. 27, 1962 A. s. CARPENTER ETAL 3,066,008 PROCESS FOR PRODUCING FIBERS FROM COPOLYMERS OF ACRYLONITRILE AND VINYLIDENE CHLORIDE Filed Feb. 25, 1960 INVINTORS ALBERT S.CARPENTER RICHARD N. TIMMS ATTORNEYS United States Patent ()1 F 3,066,008 PROCES FOR PRODUCHNG FIBERS FROM C- POLYMERS 0F ACRYLONITRILE AND VINYL- EDENE CHLORIDE Albert Stanley Carpenter, Sutton Coldfield, Birmingham,
and Richard Neville Tirnms, Coventry, England, assignors to Courtaulds Limited, London, England, 21 Butish company Fiied Feb. 25, 1960, Ser. No. 10,880 Ciainns priority, application Great Britain Mar. 9, 1959 8 Claims. (Cl. 1854) This invention relates to the manufacture of synthetic fibres and is particularly concerned with the manufacture of fibres from the copolymers of acrylonitrile and vinylidene chloride which are soluble in acetone. The invention is applicable to acetone-soluble binary copolymers of acrylonitrile and vinylidene chloride and also acetonesoluble copolymers of the two compounds with small amounts, for example up to about percent by weight, of other monomers such as vinyl pyridine or itaconic acid which may be used to modify the dyeing properties of the copolymer.
Proposals have already been made to produce acetonesoluble copolymers of acrylonitrile and vinylidene chloride, see for example British patent specification No. 643,198 and the Carpenter application Serial No. 788,045, now Patent No. 3,004,008. The acetone solutions of the copolymers may be wet or dry spun to form fibres as described for example in British patent specification No. 674,323 of British Celanese Limited. This latter specification also describes the step of stretching the resultant fibres in a heat-softened condition, for example in a hot water bath or in saturated steam; the stretching step may be followed by an annealing treatment so as to reduce the tendency of the fibres to shrink when heated to moderately elevated temperatures such as 60 to 100. C. A further type of stretching of the acrylonitrile-vinylidene chloride copolymer fibres is described in the Hampson et a1. Patent No. 2,679,450 according to which the fibers are stretched at a temperature above 120 C., for example in steam or hot water under pressure.
We have now found that it is particularly advantageous if the freshly extruded fibres of acrylonitrile-vinylidene chloride copolymers are subjected to a cold stretching operation before they are collected. The term cold stretching means that the fibres are stretched at a temperature not greater than C. In general, for economic reasons, the fibres are stretched at the ordinary temperatures. The degree of stretching should be at least 75 percent and may conveniently be from 100 to 300 percent. Throughout this specification the degree of stretching is expressed as the percentage of the increased length on the original length of the fibre; for example for a fibre stretched to twice its original length the stretch is 100 percent.
The cold stretching of the freshly extruded fibres is preferably effected between godets, the fibres leaving the spinning cell or the coagulating bath, as the case may be, being passed round a first godet and then to a second godet the peripheral speed of which is arranged to give the fibres the required degree of stretching. However, other known methods of stretching, for example using reels or rollers, or a combination of a godet and reel, may be used. Once the fibres have been cold stretched shortly after their extrusion they are preferably collected on bobbins either as twisted or untwisted yarns ready for further processing, but they may be further processed in a continuous operation.
The cold stretching is preferably elfected in air, particularly when dry spun fibres are being stretched, but stretching may be effected in water or other non-solvent estates Patented Nov. 27, 1962 at 15-40 C., and the liquid may contain a textile lubricant.
One efiect of the cold stretching operation is to make the fibres less rubbery in character. A second eifect is to reduce appreciably or to eliminate entirely the risk of stuck filaments in the collected yarn.
The fibres produced by the cold stretching operation are not however suitable for general textile uses and they are therefore given a further stretch treatment at elevated temperature. Such further stretching should be from 500 to 2,000 percent and preferably 700 to 1,500 percent. Suitable elevated temperatures are temperatures not less than C. Such hot stretching may be carried out in hot air, steam or hot water under pressure as described in the above mentioned British specification No. 674,323 and United States Patent No. 2,679,450, and the hot stretching process may be followed by an annealing treatment to reduce the shrinkage of the fibre on heating. According to a preferred embodiment of this invention the hot stretching treatment is carried out at temperatures above C. using saturated steam at superatmospheric pressure, for example up to 50 lbs. per square inch, as the heating medium. The fibres obtained as a result of stretching the cold-stretched fibres in saturated steam at superatmospheric pressure have high dimensional stabilities to wet and dry heat which are adequate for many textile purposes. In general, the fibres so stretched contract only a few percent in boiling water or in air at 136 C. and, moreover, a marked improvement in colour stability on exposure to dry heat is also obtained. If desired, still further stabilization can be effected by an annealing treatment carried out by immersing the fibres in hot or boiling water, in open steam, in steam under pressure or in hot air while allowing the natural contraction of the fibre to take place freely. For example, the fibres, after the stretching treatment in saturated steam at superatmospheric pressure, may be passed continuously, under conditions of free relaxation, through a bath of water at, or near, its boiling point (that is to say at about 90-100 C.), or through a tube containing saturated steam at atmospheric pressure. The resulting fibres show virtually no contraction on subsequent immersion in boiling water.
The present invention is illustrated by the accompanying drawings. The acetone solution of the acrylonitrilevinylidene chloride copolymer is extruded through a jet 1 within a spinning cell 2 to form filaments 3; hot air is continuously circulated within the cell 2 in known manner. The filaments 3 leaving the cell 2 are lapped round a godet 4 and are passed directly to a second godet 5 moving at 'a peripheral speed designed to stretch the filaments at least 75 percent in air between the two godets. From the godet 5 the filaments 3 are collected, without twist, on a bobbin 6.
In order to obtain the desired increase in tensile strength, the cold stretched filaments are hot stretched. Thus the filaments 3 are withdrawn from the bobbin 6 and lapped round a godet 7 before being drawn through a steam chest 8 by a godet 9 which stretches the filament in contact with the steam at least 500 percent. The hot stretched filaments are then passed by way of guides 10,.
11 to a ring spinning machine where a bobbin 12 of twisted filaments is collected.
The invention is illustrated by the following examples.
Example 1 amide solution was dissolved in acetone to give a 22 percent by weight solution. This solution was dry spun on conventional dry spinning equipment and the resulting fibres leaving the spinning cell were cold stretched 100 percent between godets and were then collected, untwisted, on a bobbin. The final collection speed was 40 metres per minute and the denier was 266. Examination of the collected yarn showed no stuck filaments and the yarn could be removed from the bobbin without difficulty, even after prolonged storage.
The yarn was then withdrawn from the bobbin and passed continuously, with stretching, through saturated steam at 30 lbs. per square inch using an apparatus consisting of two adjoining chambers, containing respectively hot water under pressure and then steam under pressure, and was finally collected as a twisted yarn. The yarn was passed into the water through a plate containing a fine orifice, and from the water into the steam through a second orifice and out of the steam through a third orifice. A godet fed the yarn to the apparatus at 2.0 metres per minute and a second godet removed it at 20.0 metres per minute and thus imposed a 900 percent stretch. The stretching tension was 2 grams. The denier of the collected yarn was 26, its tenacity was 4.35 grams denier, its extensibility was 10.7 percent and its contraction on immersion in boiling water for seconds was 4.6 percent. The cold-stretched yarn before the hot stretching process had a tenacity of 1.47 grams/denier, an extensibility of 53.8 percent and a contraction in boiling water of 37 percent.
The yarn was finally passed continuously through a bath of boiling water under conditions of free relaxation, the immersion time being 11 seconds. Its tenacity was then 3.40, grams/ denier, its extensibility 13.8 percent and its contraction in boiling water about 0.5 percent; it
showed no contraction on being heated in air at 136 C. for 1 hour.
Example 2 A copolymer of acrylonitrile and vinylidene chloride was produced by the method described in the Carpenter application Serial No. 788,045, now Patent No. 3,004,008, the copolymer containing 47 percent by weight of acrylonitrile and having an intrinsic viscosity, measured in dimethyl formamide, of 1.73. It was dissolved in acetone to produce a 22 percent by weight solution which was then dry spun through a 40 hole jet as described in Example l to produce fibres which Were stretched 100 percent at ordinary temperatures between a godet and a thread-advancing reel and then collected on bobbins without twist. The collected yarn was 900 denier/ 40 filament yarn.
The yarn was withdrawn from the bobbin by a godet having a peripheral speed of 4 metres/minute and stretched 1,150 percent in saturated steam at lbs. per
square inch by a second godet of peripheral speed 50 metres/minute; it then passed continuously at 5 0 metres/ minute through an atmosphere of saturated steam at atmospheric pressure to a godet of peripheral speed 47 metres/minute and finally collected as a twisted yarn on a ring twisting machine.
The yarn obtained had a tenacity of 4 grams/denier and an extensibility of 14 percent. It was dimensionally stable to dry and wet heat. It was woven into a fabric which was found to be flame-proof according to the British standards specification. Samples of the fabric were unaffected by contact for 5 seconds with a hot iron at temperatures up to 220 C.
What we claim is:
1. In a process for the production of fibres by extrud-- ing an acetone solution of a copolymer of acrylonitrile and vinylidene chloride through a jet into an evaporativeatmosphere within a spinning cell to form fibres and withdrawing the fibres so formed from the spinning cell,.
the step of cold stretching the fibres in air continuously with their withdrawal from the cell from to 300 percent at a temperature in the range of 15 to 40 C.
2. A process as claimed in claim 1 wherein the fibres are stretched from 1.00 to 300 percent.
3. in a process for the production of fibres by extruding an acetone solution of a copolymer of acrylonitrile and vinylidene chloride through a jet into an evaporative atmosphere within a spinning cell to form fibres and withdrawing the fibres so formed from the spinning cell, the steps or" cold stretching the fibres in air continuously with their withdrawal from the cell from 75 to 300 percent at a temperature in the range of 15 to 40 0, collecting the stretched fibres on a bobbin and subsequently withdrawing the fibres from the bobbin and stretching them a second time from 500 to 2000 percent at a temperature not less than C.
A process as claimed in claim 3 wherein the fibers are stretched in saturated steam at supcratmospheric pressure.
5. A process as claimed in claim 3 wherein the freshlyextruded fibers are first stretched from to 300 percent at a temperature in the range of 15 to 40 C. and then from 700 to 1,500- percent at a temperature not less than 95 C.
6. A process as claimed in claim 3 wherein the hotstretched fibres are subjected to an annealing treatment in which they are heated while allowing the natural contraction of the fibres to take place freely.
'7. A process as claimed in claim 6 wherein the annealing treatment is eifected in a bath of water at 90 C. to 100 C.
8. A process as claimed in claim 6 wherein the annealing treatment is effected in saturated steam at atmospheric pressure.
References Cited in the file of this patent UNITED STATES PATENTS 2,420,565 Rugeley May 13, 1947 2,681,265 Hoxie June 15, 1954 2,697,023 Martin Dec. 14, 1954 2,716,586 Terpay Aug. 30, 1955 2,775,507 Downing Dec. 25, 1956

Claims (1)

  1. 3. IN A PROCESS FOR THE PRODUCTION OF FIBERS BY EXTRUDING AN ACETONE SOLUTION OF A COPOLYMER OF ACRYLONITRILE AND VINYLIDENE CHLORIDE THROUGH A JET INTO AN EVAORATIVE ATMOSPHERE WITHIN A SPINNING CELL TO FORM FIBERS AND WITHDRAWING THE FIBERS SO FORMED FROM THE SPINNING CELL, THE STEPS OF COLD STRETCHING THE FIBERS IN AIR CONTINUOUSLY WITH THEIR WITHDRAWAL FROM THE CELL FROM 75 TO 300 PERCENT AT A TEMPERATURE IN THE RANGE OF 15* TO 40*C., COLLECTING THE STRETCHED FIBERS IN A BOBBIN AND SUBSEQUENTLY WITHDRAWING THE FIBERS FROM THE BOBBIN AND STREATCHING THEM A SECOND TIME FROM 500 TO 2000 PERCENT AT A TEMPERATURE NOT LESS THAN 95*C.
US10880A 1959-03-09 1960-02-25 Process for producing fibers from copolymers of acrylonitrile and vinylidene chloride Expired - Lifetime US3066008A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB7998/59A GB898734A (en) 1959-03-09 1959-03-09 Improvements in the manufacture of filamentary material from copolymers of acrylonitrile and vinylidene chloride

Publications (1)

Publication Number Publication Date
US3066008A true US3066008A (en) 1962-11-27

Family

ID=9843826

Family Applications (1)

Application Number Title Priority Date Filing Date
US10880A Expired - Lifetime US3066008A (en) 1959-03-09 1960-02-25 Process for producing fibers from copolymers of acrylonitrile and vinylidene chloride

Country Status (5)

Country Link
US (1) US3066008A (en)
BE (1) BE588371A (en)
ES (1) ES256346A1 (en)
GB (1) GB898734A (en)
NL (1) NL249219A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3278663A (en) * 1963-02-04 1966-10-11 Union Carbide Corp Method for producing biaxially oriented extruded polymeric film

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2658916A1 (en) * 1976-12-24 1978-07-06 Bayer Ag POLYACRYLNITRILE FILAMENT YARN

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2420565A (en) * 1943-02-20 1947-05-13 Carbide & Carbon Chem Corp Synthetic textile articles
US2681265A (en) * 1948-11-27 1954-06-15 American Viscose Corp Spinning artificial filaments
US2697023A (en) * 1950-04-29 1954-12-14 Eastman Kodak Co Spinning acrylonitrile
US2716586A (en) * 1951-09-08 1955-08-30 Ind Rayon Corp Wet spinning of acrylonitrile polymers
US2775507A (en) * 1952-01-10 1956-12-25 British Celanese Manufacture of filamentary material from copolymers of acrylonitrile and vinylidene chloride

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2420565A (en) * 1943-02-20 1947-05-13 Carbide & Carbon Chem Corp Synthetic textile articles
US2681265A (en) * 1948-11-27 1954-06-15 American Viscose Corp Spinning artificial filaments
US2697023A (en) * 1950-04-29 1954-12-14 Eastman Kodak Co Spinning acrylonitrile
US2716586A (en) * 1951-09-08 1955-08-30 Ind Rayon Corp Wet spinning of acrylonitrile polymers
US2775507A (en) * 1952-01-10 1956-12-25 British Celanese Manufacture of filamentary material from copolymers of acrylonitrile and vinylidene chloride

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3278663A (en) * 1963-02-04 1966-10-11 Union Carbide Corp Method for producing biaxially oriented extruded polymeric film

Also Published As

Publication number Publication date
GB898734A (en) 1962-06-14
BE588371A (en) 1900-01-01
NL249219A (en) 1900-01-01
ES256346A1 (en) 1960-06-16

Similar Documents

Publication Publication Date Title
US2210774A (en) Fibers from ethylene polymers
US2715763A (en) Synthetic textile fiber
US3259681A (en) Polyester filaments
US3412191A (en) Method for producing artificial fibers
US2445042A (en) Method of treating oriented acrylonitrile structures
US2346208A (en) Treatment of high tenacity yarn of synthetic origin
US2312152A (en) Rayon and method of manufacturing same
US2831748A (en) Process for melt spinning crimped filaments
US3513110A (en) Open-celled low density filamentary material
US2287099A (en) Artificial wool
US2953428A (en) Production of polychlorotrifluoroethylene textiles
US2426719A (en) Wet spinning of acrylonitrile polymers
US3415922A (en) Mist spinning
US3093444A (en) Process of preparing a helically crimped polypropylene filament
US3553305A (en) Melt-spinning process
US3233023A (en) Spinning of polypropylene
US3066008A (en) Process for producing fibers from copolymers of acrylonitrile and vinylidene chloride
US2472842A (en) Apparatus and method of dry spinning vinyl compounds
US3775961A (en) Yarn process
US3558761A (en) Method for manufacturing acrylonitrile filaments
US2988419A (en) Process for spinning and drying fibers of a polymer containing a significant amount of acrylonitrile polymerized therein
US2692185A (en) Wet spinning of acrylonitrile polymers
US2975023A (en) Production of regenerated cellulose filaments
US3424833A (en) Synthetic vinyl fibres of high shrink ability
US3493646A (en) Drawing and heat relaxing nylon yarn