DE1196317B - Verfahren zur Herstellung von Gebilden aus chlorhaltigen Polymeren - Google Patents
Verfahren zur Herstellung von Gebilden aus chlorhaltigen PolymerenInfo
- Publication number
- DE1196317B DE1196317B DEC19631A DEC0019631A DE1196317B DE 1196317 B DE1196317 B DE 1196317B DE C19631 A DEC19631 A DE C19631A DE C0019631 A DEC0019631 A DE C0019631A DE 1196317 B DE1196317 B DE 1196317B
- Authority
- DE
- Germany
- Prior art keywords
- bath
- threads
- thread
- spinning
- chlorine
- 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.)
- Pending
Links
- 229920000642 polymer Polymers 0.000 title claims description 23
- 238000000034 method Methods 0.000 title claims description 15
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 title claims description 8
- 229910052801 chlorine Inorganic materials 0.000 title claims description 8
- 239000000460 chlorine Substances 0.000 title claims description 8
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 238000009987 spinning Methods 0.000 claims description 20
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 9
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 6
- 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 claims description 5
- 229920001515 polyalkylene glycol Polymers 0.000 claims description 5
- 239000000178 monomer Substances 0.000 claims description 4
- 238000006116 polymerization reaction Methods 0.000 claims description 2
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims 1
- 229920001577 copolymer Polymers 0.000 description 10
- 239000002904 solvent Substances 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- -1 Alkyl vinyl ketones Chemical class 0.000 description 7
- 150000002334 glycols Chemical class 0.000 description 6
- 229920002959 polymer blend Polymers 0.000 description 6
- 239000003381 stabilizer Substances 0.000 description 5
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
- 239000012975 dibutyltin dilaurate Substances 0.000 description 3
- 229920001519 homopolymer Polymers 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000005033 polyvinylidene chloride Substances 0.000 description 2
- HHVIBTZHLRERCL-UHFFFAOYSA-N sulfonyldimethane Chemical compound CS(C)(=O)=O HHVIBTZHLRERCL-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- MFEVGQHCNVXMER-UHFFFAOYSA-L 1,3,2$l^{2}-dioxaplumbetan-4-one Chemical compound [Pb+2].[O-]C([O-])=O MFEVGQHCNVXMER-UHFFFAOYSA-L 0.000 description 1
- OZXIZRZFGJZWBF-UHFFFAOYSA-N 1,3,5-trimethyl-2-(2,4,6-trimethylphenoxy)benzene Chemical compound CC1=CC(C)=CC(C)=C1OC1=C(C)C=C(C)C=C1C OZXIZRZFGJZWBF-UHFFFAOYSA-N 0.000 description 1
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 1
- QQZOPKMRPOGIEB-UHFFFAOYSA-N 2-Oxohexane Chemical compound CCCCC(C)=O QQZOPKMRPOGIEB-UHFFFAOYSA-N 0.000 description 1
- VGVHNLRUAMRIEW-UHFFFAOYSA-N 4-methylcyclohexan-1-one Chemical compound CC1CCC(=O)CC1 VGVHNLRUAMRIEW-UHFFFAOYSA-N 0.000 description 1
- VJOWMORERYNYON-UHFFFAOYSA-N 5-ethenyl-2-methylpyridine Chemical compound CC1=CC=C(C=C)C=N1 VJOWMORERYNYON-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- HETCEOQFVDFGSY-UHFFFAOYSA-N Isopropenyl acetate Chemical compound CC(=C)OC(C)=O HETCEOQFVDFGSY-UHFFFAOYSA-N 0.000 description 1
- 229910000003 Lead carbonate Inorganic materials 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 150000001553 barium compounds Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000001112 coagulating effect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000005670 ethenylalkyl group Chemical group 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- YJOMWQQKPKLUBO-UHFFFAOYSA-L lead(2+);phthalate Chemical compound [Pb+2].[O-]C(=O)C1=CC=CC=C1C([O-])=O YJOMWQQKPKLUBO-UHFFFAOYSA-L 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- SHOJXDKTYKFBRD-UHFFFAOYSA-N mesityl oxide Natural products CC(C)=CC(C)=O SHOJXDKTYKFBRD-UHFFFAOYSA-N 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 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
- D01F6/08—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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Artificial Filaments (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US755379A US3011859A (en) | 1958-08-18 | 1958-08-18 | Manufacture of polymeric shaped objects by wet spinning |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1196317B true DE1196317B (de) | 1965-07-08 |
Family
ID=25038882
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEC19631A Pending DE1196317B (de) | 1958-08-18 | 1959-08-18 | Verfahren zur Herstellung von Gebilden aus chlorhaltigen Polymeren |
| DE1959C0019630 Pending DE1288240B (de) | 1958-08-18 | 1959-08-18 | Verfahren zum Herstellen von Faeden aus Acrylnitrolpolymerisaten durch Nassspinnen |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE1959C0019630 Pending DE1288240B (de) | 1958-08-18 | 1959-08-18 | Verfahren zum Herstellen von Faeden aus Acrylnitrolpolymerisaten durch Nassspinnen |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3011859A (forum.php) |
| BE (1) | BE581752A (forum.php) |
| CH (1) | CH395423A (forum.php) |
| DE (2) | DE1196317B (forum.php) |
| FR (1) | FR1233863A (forum.php) |
| GB (1) | GB888343A (forum.php) |
| NL (1) | NL242435A (forum.php) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE624420A (forum.php) * | 1961-11-07 | 1900-01-01 | ||
| NL298105A (forum.php) * | 1962-09-27 | |||
| US3327037A (en) * | 1962-12-24 | 1967-06-20 | Snia Viscosa | Process for the spinning of the crystalline polymer of vinyl chloride |
| US3619453A (en) * | 1969-11-03 | 1971-11-09 | Celanese Corp | Wet spinning process for the production of polybenzimidazole filaments |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE496324A (forum.php) * | 1949-06-13 | |||
| US2642333A (en) * | 1949-07-26 | 1953-06-16 | Omni Products Corp | Method of spinning polyvinyl alcohol fibers |
| US2742444A (en) * | 1951-10-09 | 1956-04-17 | Eastman Kodak Co | Solutions of polymers of vinylidene chloride |
| US2761855A (en) * | 1952-05-05 | 1956-09-04 | Chemstrand Corp | Polymeric vinyl chloride fiberforming compositions |
| US2773114A (en) * | 1954-08-31 | 1956-12-04 | Us Rubber Co | Battery separator and method of making same |
-
0
- NL NL242435D patent/NL242435A/xx unknown
-
1958
- 1958-08-18 US US755379A patent/US3011859A/en not_active Expired - Lifetime
-
1959
- 1959-08-11 CH CH7681359A patent/CH395423A/fr unknown
- 1959-08-11 GB GB27460/59A patent/GB888343A/en not_active Expired
- 1959-08-14 FR FR802917A patent/FR1233863A/fr not_active Expired
- 1959-08-17 BE BE581752D patent/BE581752A/xx unknown
- 1959-08-18 DE DEC19631A patent/DE1196317B/de active Pending
- 1959-08-18 DE DE1959C0019630 patent/DE1288240B/de active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| BE581752A (forum.php) | 1960-02-17 |
| US3011859A (en) | 1961-12-05 |
| FR1233863A (fr) | 1960-10-12 |
| NL242435A (forum.php) | |
| GB888343A (en) | 1962-01-31 |
| CH395423A (fr) | 1965-07-15 |
| DE1288240B (de) | 1969-01-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2458912C2 (forum.php) | ||
| EP0044534B1 (de) | Hochmodul-Polyacrylnitrilfäden und -fasern sowie Verfahren zu ihrer Herstellung | |
| DE2403947A1 (de) | Schmelzspinnverfahren zur herstellung von geformten gegenstaenden aus acrylnitrilpolymerisaten | |
| DE1030970B (de) | Verfahren zur Herstellung von Faeden und Fasern aus Polyacrylsaeurenitril | |
| DE1247640B (de) | Verfahren zur Herstellung von Faeden oder Formkoerpern aus Polypropylen | |
| EP0019870B1 (de) | Fäden und Fasern aus Acrylnitril-Copolymer-Mischungen sowie Verfahren zu ihrer Herstellung | |
| DE1256838B (de) | Verfahren zum Herstellen von Faeden durch Nassverspinnen einer Polyvinylidenfluoridloesung | |
| DE1196317B (de) | Verfahren zur Herstellung von Gebilden aus chlorhaltigen Polymeren | |
| DE1292310B (de) | Verfahren zur Herstellung von Fasern und Faeden aus Acrylnitrilpolymerisaten | |
| DE1286684B (de) | Verfahren zur Herstellung von Faeden, Fasern oder Folien durch Nass- oder Trockenverspinnen einer Acrylnitrilpolymerisatmischung | |
| DE1270216B (de) | Verfahren zur herstellung von faeden aus linearen polyestern | |
| DE2009708B2 (de) | NaBspinnverfahren zur Herstellung von Fäden aus einer Spinnlösung von Acrylnitrilmischpolymerisaten | |
| DE1469093C3 (de) | Verfahren zur Herstellung von PoIycarbonatfäden oder -fasern | |
| DE1201003B (de) | Verfahren zur Herstellung von gut anfaerbbaren Faeden oder Fasern aus Polyvinylalkohol | |
| DE1278066B (de) | Verfahren zur Herstellung von Faeden, die ueberwiegend aus Polyvinylchlorid hochsyndiotaktischen Grades bestehen | |
| DE3630244C2 (de) | Kontinuierliches Trockenspinn- und Nachbehandlungsverfahren des Spinngutes für hochschrumpffähige Acrylnitrilfäden und -fasern und entsprechende Fäden und Fasern | |
| DE3634753C2 (forum.php) | ||
| DE1807781A1 (de) | Verfahren zum Herstellen von Akrylnitril-Synthese-Fasern | |
| DE1224872B (de) | Herstellen von Faeden oder Fasern aus vinylidencyanidhaltigen Mischpolymerisaten | |
| DE1569139C (de) | Stabilisierung von Acrylnitril/ Vinylchlorid Mischpolymerisaten bzw Polymerisat Gemischen | |
| DE1069819B (forum.php) | ||
| DE2164917A1 (de) | Modacrylfaeden und -fasern, die beim kontakt mit heissem wasser glaenzend und transparent bleiben, sowie verfahren zu ihrer herstellung | |
| DE1494601A1 (de) | Verfahren zur Herstellung von Faeden aus Beta-Polyamiden | |
| DE2854314A1 (de) | Verfahren zur herstellung von hydrophilen faeden oder fasern aus einem acrylnitrilhomo- oder acrylnitrilmischpolymerisat | |
| DE1937266C (de) | Verfahren zur Herstellung von Faden aus Acrylnitrilpolymensaten |