DE1062883B - Verfahren zur Herstellung von verformbaren Polyvinylidencyanid-loesungen - Google Patents
Verfahren zur Herstellung von verformbaren Polyvinylidencyanid-loesungenInfo
- Publication number
- DE1062883B DE1062883B DEG21042A DEG0021042A DE1062883B DE 1062883 B DE1062883 B DE 1062883B DE G21042 A DEG21042 A DE G21042A DE G0021042 A DEG0021042 A DE G0021042A DE 1062883 B DE1062883 B DE 1062883B
- Authority
- DE
- Germany
- Prior art keywords
- vinylidenecyanide
- copolymers
- polymer
- solutions
- solvent
- 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
- 238000000034 method Methods 0.000 title claims description 9
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- 229920001577 copolymer Polymers 0.000 claims description 32
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 22
- FCYVWWWTHPPJII-UHFFFAOYSA-N 2-methylidenepropanedinitrile Chemical compound N#CC(=C)C#N FCYVWWWTHPPJII-UHFFFAOYSA-N 0.000 claims description 18
- 239000002904 solvent Substances 0.000 claims description 17
- 229920000642 polymer Polymers 0.000 claims description 13
- 239000000178 monomer Substances 0.000 claims description 9
- 150000003462 sulfoxides Chemical class 0.000 claims description 9
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 6
- -1 methylethyl Chemical group 0.000 claims description 5
- 239000004215 Carbon black (E152) Substances 0.000 claims description 3
- 229930195733 hydrocarbon Natural products 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 229920000131 polyvinylidene Polymers 0.000 claims description 2
- 239000000243 solution Substances 0.000 claims 16
- 239000000203 mixture Substances 0.000 claims 9
- 238000009987 spinning Methods 0.000 claims 6
- 238000005266 casting Methods 0.000 claims 5
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims 3
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims 3
- 150000001875 compounds Chemical class 0.000 claims 3
- 229920001897 terpolymer Polymers 0.000 claims 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims 2
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000002573 ethenylidene group Chemical class [*]=C=C([H])[H] 0.000 claims 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims 2
- 150000002825 nitriles Chemical class 0.000 claims 2
- 239000002245 particle Substances 0.000 claims 2
- UKDOTCFNLHHKOF-FGRDZWBJSA-N (z)-1-chloroprop-1-ene;(z)-1,2-dichloroethene Chemical group C\C=C/Cl.Cl\C=C/Cl UKDOTCFNLHHKOF-FGRDZWBJSA-N 0.000 claims 1
- UPVJEODAZWTJKZ-UHFFFAOYSA-N 1,2-dichloro-1,2-difluoroethene Chemical group FC(Cl)=C(F)Cl UPVJEODAZWTJKZ-UHFFFAOYSA-N 0.000 claims 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 claims 1
- WYFCZWSWFGJODV-MIANJLSGSA-N 4-[[(1s)-2-[(e)-3-[3-chloro-2-fluoro-6-(tetrazol-1-yl)phenyl]prop-2-enoyl]-5-(4-methyl-2-oxopiperazin-1-yl)-3,4-dihydro-1h-isoquinoline-1-carbonyl]amino]benzoic acid Chemical compound O=C1CN(C)CCN1C1=CC=CC2=C1CCN(C(=O)\C=C\C=1C(=CC=C(Cl)C=1F)N1N=NN=C1)[C@@H]2C(=O)NC1=CC=C(C(O)=O)C=C1 WYFCZWSWFGJODV-MIANJLSGSA-N 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 1
- OSDWBNJEKMUWAV-UHFFFAOYSA-N Allyl chloride Chemical compound ClCC=C OSDWBNJEKMUWAV-UHFFFAOYSA-N 0.000 claims 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims 1
- DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical compound C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 claims 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims 1
- 238000005054 agglomeration Methods 0.000 claims 1
- 230000002776 aggregation Effects 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- PDEXWJGSZIRHMS-UHFFFAOYSA-N chloro(chloromethylsulfinyl)methane Chemical compound ClCS(=O)CCl PDEXWJGSZIRHMS-UHFFFAOYSA-N 0.000 claims 1
- CCAFPWNGIUBUSD-UHFFFAOYSA-N diethyl sulfoxide Chemical compound CCS(=O)CC CCAFPWNGIUBUSD-UHFFFAOYSA-N 0.000 claims 1
- FDPIMTJIUBPUKL-UHFFFAOYSA-N dimethylacetone Natural products CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 claims 1
- 239000006185 dispersion Substances 0.000 claims 1
- 238000004090 dissolution Methods 0.000 claims 1
- LYABNKDOHBOTFF-UHFFFAOYSA-N ethenyl acetate;2-methylidenepropanedinitrile Chemical compound CC(=O)OC=C.N#CC(=C)C#N LYABNKDOHBOTFF-UHFFFAOYSA-N 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 238000002844 melting Methods 0.000 claims 1
- 230000008018 melting Effects 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 239000011259 mixed solution Substances 0.000 claims 1
- 125000004957 naphthylene group Chemical group 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 claims 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
- 238000003756 stirring Methods 0.000 claims 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 claims 1
- 229920001959 vinylidene polymer Polymers 0.000 claims 1
- 239000000126 substance Substances 0.000 description 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- LFSHREXVLSTLFB-UHFFFAOYSA-N 1-cyanoethenyl acetate Chemical compound CC(=O)OC(=C)C#N LFSHREXVLSTLFB-UHFFFAOYSA-N 0.000 description 1
- LPVVECYRRCOUJE-UHFFFAOYSA-N CC(C(C#N)O)(C#N)C Chemical compound CC(C(C#N)O)(C#N)C LPVVECYRRCOUJE-UHFFFAOYSA-N 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
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- BEPAFCGSDWSTEL-UHFFFAOYSA-N dimethyl malonate Chemical compound COC(=O)CC(=O)OC BEPAFCGSDWSTEL-UHFFFAOYSA-N 0.000 description 1
- GAEKPEKOJKCEMS-UHFFFAOYSA-N gamma-valerolactone Chemical compound CC1CCC(=O)O1 GAEKPEKOJKCEMS-UHFFFAOYSA-N 0.000 description 1
- WYVAMUWZEOHJOQ-UHFFFAOYSA-N propionic anhydride Chemical compound CCC(=O)OC(=O)CC WYVAMUWZEOHJOQ-UHFFFAOYSA-N 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C08J3/097—Sulfur containing compounds
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Artificial Filaments (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polymerisation Methods In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US358235XA | 1955-12-09 | 1955-12-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1062883B true DE1062883B (de) | 1959-08-06 |
Family
ID=21884983
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEG21042A Pending DE1062883B (de) | 1955-12-09 | 1956-12-05 | Verfahren zur Herstellung von verformbaren Polyvinylidencyanid-loesungen |
Country Status (5)
Country | Link |
---|---|
CH (1) | CH358235A (enrdf_load_stackoverflow) |
DE (1) | DE1062883B (enrdf_load_stackoverflow) |
FR (1) | FR1165587A (enrdf_load_stackoverflow) |
GB (1) | GB809346A (enrdf_load_stackoverflow) |
NL (2) | NL212799A (enrdf_load_stackoverflow) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3165488A (en) * | 1959-12-15 | 1965-01-12 | Kurashiki Rayon Co | Spinning solutions of a mixture of polyvinyl alcohol and a vinyl acetate-vinylidene cyanide copolymer in dimethyl sulfoxide and fibers therefrom |
US3474163A (en) * | 1967-11-22 | 1969-10-21 | Celanese Corp | Process of spinning filaments of vinylidene cyanide |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB654957A (en) * | 1948-02-26 | 1951-07-04 | Goodrich Co B F | Improvements in or relating to polymers and polymer products |
-
0
- NL NL95714D patent/NL95714C/xx active
- NL NL212799D patent/NL212799A/xx unknown
-
1956
- 1956-11-28 GB GB36366/56A patent/GB809346A/en not_active Expired
- 1956-12-04 FR FR1165587D patent/FR1165587A/fr not_active Expired
- 1956-12-05 DE DEG21042A patent/DE1062883B/de active Pending
- 1956-12-08 CH CH358235D patent/CH358235A/fr unknown
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB654957A (en) * | 1948-02-26 | 1951-07-04 | Goodrich Co B F | Improvements in or relating to polymers and polymer products |
Also Published As
Publication number | Publication date |
---|---|
NL95714C (enrdf_load_stackoverflow) | |
FR1165587A (fr) | 1958-10-27 |
GB809346A (en) | 1959-02-25 |
CH358235A (fr) | 1961-11-15 |
NL212799A (enrdf_load_stackoverflow) |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE972816C (de) | Verfahren zur Herstellung klarer und im wesentlichen farbloser Loesungen von Acrylsaeurenitrilpolymeren | |
DE916348C (de) | Plastische, polymere Massen, insbesondere fuer die Herstellung von kuenstlichen Gebilden, wie Faeden oder Fasern | |
DE920206C (de) | Verfahren zur Herstellung von formbaren Massen auf der Grundlage von Acrylsaeurenitrilpolymerisaten | |
DE1570771C3 (de) | Verfahren zur Herstellung einer stabilen Dispersion aus einem synthetischem Polymer in einer organischen Flüssigkeit | |
DE2637603C2 (de) | Beständige Latices von Styrolhomo- oder -copolymerisaten, Verfahren zu ihrer Herstellung und ihre Verwendung | |
DE1921946B2 (de) | Verfahren zur herstellung von waessrigen dispersionen von polymerisaten olefinisch ungesaettigter monomerer | |
DE2433486C3 (de) | Verfahren zur Herstellung von Emulsionen, konzentrierten Dispersionen und Pasten von hydrophilen polymeren Füllstoffen in Weichmachern | |
DE1062883B (de) | Verfahren zur Herstellung von verformbaren Polyvinylidencyanid-loesungen | |
DE1645329A1 (de) | Verfahren zum Unterbrechen der Tieftemperaturpolymerisation von Vinylchlorid | |
US2588335A (en) | Solutions of acrylonitrile polymers | |
DE906515C (de) | Verfahren zur Herstellung von Polyacrylsaeurenitril- oder Acrylsaeurenitrilmischpolymerisat-Weichmacher-Mischungen | |
DE2050723C3 (de) | Verfahren zur Herstellung von Vinylchloridpolymerisaten | |
DE1138921B (de) | Schlagfeste thermoplastische Kunststoff-Formmassen | |
DE862368C (de) | Verfahren zur Herstellung von Loesungen von Acrylnitrilpolymeren | |
DE962651C (de) | Verfahren zur Herstellung von Filmen, Fasern und anderen geformten Gegenstaenden aus Polymerisaten bzw. Mischpolymerisaten, die mehr als 50% Chloracrylnitril enthalten | |
DE968130C (de) | Verfahren zur Herstellung pulver- oder kornfoermiger Mischpolymerisate aus Maleinsaeureanhydrid und Styrol bzw. Styrol-Derivaten | |
DE855161C (de) | Verfahren zur Herstellung von Mischpolymerisaten aus Acrylsaeurenitril und Vinylpyridinen | |
AT247001B (de) | Verfahren zur Herstellung von Copolyestern | |
DE953659C (de) | Verfahren zur Herstellung von Mischpolymerisaten auf Grundlage von Vinylidencyanid | |
DE879017C (de) | Verfahren zur Herstellung von Polymerisationsprodukten | |
DE1093557B (de) | Verfahren zur Herstellung von weitgehend thermostabilen Acrylnitril-Polymerisaten mit verbesserter Anfaerbbarkeit gegenueber basischen Farbstoffen | |
DE2714948A1 (de) | Verfahren zur kontinuierlichen herstellung von vinylchlorid-polymerisaten | |
DE1494048B2 (de) | Verfahren zur herstellung von loesungen aus acrylnitril polymerisaten in organischen loesungsmitteln | |
DE923507C (de) | Verfahren zur Polymerisation von Acrylnitrilen mit Vinylpyridinen | |
DE821554C (de) | Verfahren zur Herstellung von Polymerisaten und Mischpolymerisaten von Vinylverbindungen |