DE1770268B2 - Verfahren zur Herstellung von Polythioathern - Google Patents
Verfahren zur Herstellung von PolythioathernInfo
- Publication number
- DE1770268B2 DE1770268B2 DE1770268A DE1770268A DE1770268B2 DE 1770268 B2 DE1770268 B2 DE 1770268B2 DE 1770268 A DE1770268 A DE 1770268A DE 1770268 A DE1770268 A DE 1770268A DE 1770268 B2 DE1770268 B2 DE 1770268B2
- Authority
- DE
- Germany
- Prior art keywords
- hccl
- diphenyl
- sulfur
- parts
- aluminum
- 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 11
- 229920006295 polythiol Polymers 0.000 title description 6
- 238000002360 preparation method Methods 0.000 title description 5
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims description 12
- 239000003054 catalyst Substances 0.000 claims description 7
- PXJJSXABGXMUSU-UHFFFAOYSA-N disulfur dichloride Chemical compound ClSSCl PXJJSXABGXMUSU-UHFFFAOYSA-N 0.000 claims description 7
- 229920000642 polymer Polymers 0.000 claims description 7
- FWMUJAIKEJWSSY-UHFFFAOYSA-N sulfur dichloride Chemical compound ClSCl FWMUJAIKEJWSSY-UHFFFAOYSA-N 0.000 claims description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 5
- LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical compound C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 claims description 4
- 238000000921 elemental analysis Methods 0.000 claims description 4
- 229910000761 Aluminium amalgam Inorganic materials 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- 239000004305 biphenyl Substances 0.000 claims description 3
- 235000010290 biphenyl Nutrition 0.000 claims description 3
- 125000006267 biphenyl group Chemical group 0.000 claims description 3
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 claims description 3
- 229910052742 iron Inorganic materials 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 3
- 238000002329 infrared spectrum Methods 0.000 claims description 2
- 238000001228 spectrum Methods 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims 1
- 210000003298 dental enamel Anatomy 0.000 claims 1
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 claims 1
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N dimethylformamide Substances CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 5
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 4
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 4
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 150000001491 aromatic compounds Chemical class 0.000 description 2
- QGJOPFRUJISHPQ-NJFSPNSNSA-N carbon disulfide-14c Chemical compound S=[14C]=S QGJOPFRUJISHPQ-NJFSPNSNSA-N 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 238000002074 melt spinning Methods 0.000 description 2
- -1 phenyl radicals Chemical class 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000001226 reprecipitation Methods 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- HAHPGQIYPXCFBI-UHFFFAOYSA-N CC(=O)C.N1CCOCC1 Chemical compound CC(=O)C.N1CCOCC1 HAHPGQIYPXCFBI-UHFFFAOYSA-N 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- HOPRXXXSABQWAV-UHFFFAOYSA-N anhydrous collidine Natural products CC1=CC=NC(C)=C1C HOPRXXXSABQWAV-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- UTBIMNXEDGNJFE-UHFFFAOYSA-N collidine Natural products CC1=CC=C(C)C(C)=N1 UTBIMNXEDGNJFE-UHFFFAOYSA-N 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 238000007323 disproportionation reaction Methods 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- GFYHSKONPJXCDE-UHFFFAOYSA-N sym-collidine Natural products CC1=CN=C(C)C(C)=C1 GFYHSKONPJXCDE-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/0204—Polyarylenethioethers
- C08G75/025—Preparatory processes
- C08G75/0268—Preparatory processes using disulfides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/0204—Polyarylenethioethers
- C08G75/0227—Polyarylenethioethers derived from monomers containing two or more aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/0204—Polyarylenethioethers
- C08G75/025—Preparatory processes
- C08G75/0272—Preparatory processes using other sulfur sources
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/12—Polythioether-ethers
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2670467A JPS4627255B1 (enExample) | 1967-04-25 | 1967-04-25 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE1770268A1 DE1770268A1 (de) | 1972-04-06 |
| DE1770268B2 true DE1770268B2 (de) | 1973-10-31 |
Family
ID=12200762
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE1770268A Pending DE1770268B2 (de) | 1967-04-25 | 1968-04-25 | Verfahren zur Herstellung von Polythioathern |
Country Status (4)
| Country | Link |
|---|---|
| JP (1) | JPS4627255B1 (enExample) |
| DE (1) | DE1770268B2 (enExample) |
| FR (1) | FR1589417A (enExample) |
| GB (1) | GB1213678A (enExample) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0678556A1 (en) | 1988-11-08 | 1995-10-25 | Ge Plastics Japan Limited | Polyphenylene sulfide resin composition |
| EP0440106A3 (en) * | 1990-01-29 | 1992-05-20 | Seisan Kaihatsu Kagaku Kenkyusho | Process for preparing polyarylene thioethers |
| WO2007114056A1 (ja) | 2006-03-30 | 2007-10-11 | Asahi Kasei Chemicals Corporation | 樹脂組成物およびその成形品 |
| WO2008102851A1 (ja) | 2007-02-21 | 2008-08-28 | Asahi Kasei E-Materials Corporation | 高分子電解質組成物、高分子電解質膜、膜電極接合体、及び固体高分子電解質型燃料電池 |
| US20140335440A1 (en) | 2011-09-21 | 2014-11-13 | Toray Industries, Inc. | Molded article of polymer electrolyte composition and solid polymer type fuel cell using same |
| JP6002685B2 (ja) | 2011-12-28 | 2016-10-05 | 旭化成株式会社 | レドックスフロー二次電池及びレドックスフロー二次電池用電解質膜 |
| JP6418852B2 (ja) | 2014-09-05 | 2018-11-07 | 株式会社クレハ | ポリアリーレンスルフィドの製造方法及びポリアリーレンスルフィド |
| US20190226525A1 (en) | 2016-09-28 | 2019-07-25 | Ntn Corporation | Sliding member |
| WO2018207325A1 (ja) | 2017-05-11 | 2018-11-15 | 旭化成株式会社 | 高分子電解質膜、膜電極接合体、及び固体高分子型燃料電池 |
| WO2019078303A1 (ja) | 2017-10-18 | 2019-04-25 | Ntn株式会社 | カバーおよび車載用フィン型アンテナ装置 |
| EP4383457A4 (en) | 2021-08-05 | 2024-12-11 | Asahi Kasei Kabushiki Kaisha | ANTENNA ELEMENT |
| JPWO2024185634A1 (enExample) * | 2023-03-07 | 2024-09-12 |
-
1967
- 1967-04-25 JP JP2670467A patent/JPS4627255B1/ja active Pending
-
1968
- 1968-04-16 GB GB07783/68A patent/GB1213678A/en not_active Expired
- 1968-04-24 FR FR1589417D patent/FR1589417A/fr not_active Expired
- 1968-04-25 DE DE1770268A patent/DE1770268B2/de active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| DE1770268A1 (de) | 1972-04-06 |
| FR1589417A (enExample) | 1970-03-31 |
| JPS4627255B1 (enExample) | 1971-08-07 |
| GB1213678A (en) | 1970-11-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1770268B2 (de) | Verfahren zur Herstellung von Polythioathern | |
| DE2648470A1 (de) | Poly(arylat-sulfone) und verfahren zu ihrer herstellung | |
| DE2438327C2 (de) | Polyätherchinoxaline und Verfahren zu deren Herstellung | |
| DE3686339T2 (de) | Copolymere und verfahren zu ihrer herstellung. | |
| DE1595781C3 (de) | Verfahren zur Herstellung hochmolekularer, thermoplastischer Polyester. Ausscheidung aus: 1445384 | |
| EP0175205B1 (de) | Hochmolekulare Polyester, ihre Herstellung und Verwendung | |
| DE2428124A1 (de) | Verfahren zur herstellung von poly(halogenaryloxyphosphazen)-homopolymeren | |
| DE3725997A1 (de) | Verfahren zur herstellung von polyarylensulfiden | |
| DE2508710A1 (de) | 1,1,2-tris-(p-hydroxyphenyl)-1- phenyl-aethane sowie ein verfahren zu ihrer herstellung | |
| DE1235900B (de) | Verfahren zur Herstellung von Hexabrom-, Tetrabrom-, Tetrabromdichlor- oder Dibromdichlordiphenylsulfiden | |
| DE1495621A1 (de) | Verfahren zur Verbesserung der physikalischen Eigenschaften von Polycarbonaten | |
| DE2529487C2 (de) | Verfahren zur Herstellung hochreiner, mehrwertiger Cyansäureester | |
| DE1493430A1 (de) | Verfahren zur Herstellung aromatischer Saeuren sowie neuer Ester und Polyester | |
| DE3521123A1 (de) | Phosphorhaltige polyarylenaether und verfahren zu ihrer herstellung | |
| DE1595579B2 (enExample) | ||
| DE2701096C2 (de) | Thermoplastische Polybibenzylsulfon-Polymere | |
| DE1221448B (de) | Verfahren zur Herstellung von Copolymerisaten | |
| DE2441105A1 (de) | Verfahren zur herstellung aromatischer polymere | |
| DE2856966A1 (de) | Solution polymerized halogenated polyesters | |
| DE3231331A1 (de) | Phosphorhaltige polyarylenester und verfahren zu ihrer herstellung | |
| DE861610C (de) | Verfahren zur Herstellung von Polythioestern | |
| DE1620971B2 (de) | Verfahren zur Herstellung von Poly furoxanen | |
| DE2052378C3 (de) | Halogenhaltige hochmolekulare aromatische Polyestercarbonate, Verfahren zu ihrer Herstellung und ihre Verwendung | |
| DE1595630C3 (de) | Verfahren zur Herstellung von spinnfähigen Acrylnitrll-Polymerisatlösungen | |
| EP0297037A1 (de) | Poly(arylensulfide) |