GB711344A - Improvements in the production of filaments, films and like shaped articles from acrylonitrile polymers - Google Patents
Improvements in the production of filaments, films and like shaped articles from acrylonitrile polymersInfo
- Publication number
- GB711344A GB711344A GB2318450A GB2318450A GB711344A GB 711344 A GB711344 A GB 711344A GB 2318450 A GB2318450 A GB 2318450A GB 2318450 A GB2318450 A GB 2318450A GB 711344 A GB711344 A GB 711344A
- Authority
- GB
- United Kingdom
- Prior art keywords
- per cent
- solution
- filaments
- dimethyl formamide
- films
- 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
Links
- 229920002239 polyacrylonitrile Polymers 0.000 title abstract 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 abstract 12
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 5
- 230000001112 coagulating effect Effects 0.000 abstract 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 abstract 3
- 239000007788 liquid Substances 0.000 abstract 3
- 239000002904 solvent Substances 0.000 abstract 3
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 abstract 2
- 239000000470 constituent Substances 0.000 abstract 2
- 235000019441 ethanol Nutrition 0.000 abstract 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 abstract 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 abstract 2
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 abstract 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 abstract 1
- VUZPGEIXNYGDJN-UHFFFAOYSA-N 1-nitroethanol Chemical compound CC(O)[N+]([O-])=O VUZPGEIXNYGDJN-UHFFFAOYSA-N 0.000 abstract 1
- FRSSCXBIIPYXOU-UHFFFAOYSA-N 1-nitropropan-1-ol Chemical compound CCC(O)[N+]([O-])=O FRSSCXBIIPYXOU-UHFFFAOYSA-N 0.000 abstract 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 abstract 1
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 abstract 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 abstract 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 abstract 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 abstract 1
- 125000005396 acrylic acid ester group Chemical group 0.000 abstract 1
- 150000004996 alkyl benzenes Chemical class 0.000 abstract 1
- 125000003180 beta-lactone group Chemical group 0.000 abstract 1
- VEZXCJBBBCKRPI-UHFFFAOYSA-N beta-propiolactone Chemical compound O=C1CCO1 VEZXCJBBBCKRPI-UHFFFAOYSA-N 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- -1 cyclic aliphatic anhydrides Chemical class 0.000 abstract 1
- 235000019253 formic acid Nutrition 0.000 abstract 1
- VANNPISTIUFMLH-UHFFFAOYSA-N glutaric anhydride Chemical compound O=C1CCCC(=O)O1 VANNPISTIUFMLH-UHFFFAOYSA-N 0.000 abstract 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- WRAQQYDMVSCOTE-UHFFFAOYSA-N phenyl prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1 WRAQQYDMVSCOTE-UHFFFAOYSA-N 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 229960000380 propiolactone Drugs 0.000 abstract 1
- 229940014800 succinic anhydride Drugs 0.000 abstract 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- 239000008096 xylene Substances 0.000 abstract 1
- 150000003738 xylenes Chemical class 0.000 abstract 1
Classifications
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Artificial Filaments (AREA)
Abstract
A solution of a fibre-forming acrylonitrile polymer is shaped and set by a coagulating medium comprising as the chief or sole constituent a liquid aromatic hydrocarbon or a liquid halogenated aliphatic hydrocarbon to form filaments, films and other shaped articles. The term acrylonitrile polymer includes copolymers in which acrylonitrile is the main constituent (especially exceeding 85 per cent.) with methacrylonitrile, vinyl chloride, vinyl acetate, acrylic acid esters such as methyl and phenyl acrylate, styrene and its derivatives and vinylidene chloride. Aromatic hydrocarbons, especially benzene, toluene, the xylenes and alkyl benzenes such as solvent naphtha are preferred as the coagulating medium. Chlorinated paraffins such as carbon tetrachloride, ethylene dichloride and symmetrical tetrachlorethane may also be used. If desired, a more polar liquid such as ethanol may be added to the coagulating medium in an amount up to 30 per cent. by volume or the limit of miscibility with the aromatic hydrocarbon or halogenated aliphatic hydrocarbon, whichever is the lower. The acrylonitrile polymer may be dissolved in dimethyl formamide, gamma-butyrolactone, gamma- and delta-valerolactones, propiolactone and other beta-lactones, tetramethylene sulphone and solvents comprising nitromethane with or without formic acid. Dimethyl formamide or a mixture of nitromethane and a minor proportion but at least 6 per cent. of water are preferred. Preferably the polymer has a viscosity in 1 per cent. solution in dimethyl formamide at 20 DEG C. of between 2.5 and 4 centistokes. The solution to be extruded or cast may have a concentration between 7.5 and 25 per cent. and the temperature should be high enough to maintain solution. The temperature of the coagulating medium may be preferably between 50 and 100 DEG C. The filaments films and other shaped articles may be stretched or relaxed by known methods. In an example a 20 per cent. solution of polyacrylonitrile (viscosity 2.52 centistokes) in dimethyl formamide at 40 DEG C. is extruded as filaments into benzene or a 5:1 by volume benzene/ethyl alcohol mixture at 60 DEG C. The Provisional p Specification also refers to the following as suitable solvents for the acrylonitrile polymer: nitro ethanol, nitro propanol, and cyclic aliphatic anhydrides such as maleic anhydride, succinic anhydride and glutaric anhydride. Specification 690,553 is referred to.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2318450A GB711344A (en) | 1950-09-21 | 1950-09-21 | Improvements in the production of filaments, films and like shaped articles from acrylonitrile polymers |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2318450A GB711344A (en) | 1950-09-21 | 1950-09-21 | Improvements in the production of filaments, films and like shaped articles from acrylonitrile polymers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB711344A true GB711344A (en) | 1954-06-30 |
Family
ID=10191510
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2318450A Expired GB711344A (en) | 1950-09-21 | 1950-09-21 | Improvements in the production of filaments, films and like shaped articles from acrylonitrile polymers |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB711344A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1272485B (en) * | 1954-10-25 | 1968-07-11 | Fosfatbolaget Aktiebolag | Process for the production of threads or fibers by wet spinning of acrylonitrile copolymers |
| US3491179A (en) * | 1967-01-03 | 1970-01-20 | American Cyanamid Co | Preparation of acrylonitrile polymer fibers |
| US3984515A (en) * | 1972-03-07 | 1976-10-05 | Akzo Belge S.A. | Polyacrylonitrile fibers having a natural crimp and process for producing the same |
| WO2001027371A1 (en) * | 1999-10-08 | 2001-04-19 | 3M Innovative Properties Company | Method and apparatus for making a nonwoven fibrous electret web from free-fiber and polar liquid |
-
1950
- 1950-09-21 GB GB2318450A patent/GB711344A/en not_active Expired
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1272485B (en) * | 1954-10-25 | 1968-07-11 | Fosfatbolaget Aktiebolag | Process for the production of threads or fibers by wet spinning of acrylonitrile copolymers |
| US3491179A (en) * | 1967-01-03 | 1970-01-20 | American Cyanamid Co | Preparation of acrylonitrile polymer fibers |
| US3984515A (en) * | 1972-03-07 | 1976-10-05 | Akzo Belge S.A. | Polyacrylonitrile fibers having a natural crimp and process for producing the same |
| WO2001027371A1 (en) * | 1999-10-08 | 2001-04-19 | 3M Innovative Properties Company | Method and apparatus for making a nonwoven fibrous electret web from free-fiber and polar liquid |
| US6375886B1 (en) | 1999-10-08 | 2002-04-23 | 3M Innovative Properties Company | Method and apparatus for making a nonwoven fibrous electret web from free-fiber and polar liquid |
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