DE2637534C2 - Verfahren zum Polymerisieren von cyclischen Phosphazenen - Google Patents
Verfahren zum Polymerisieren von cyclischen PhosphazenenInfo
- Publication number
- DE2637534C2 DE2637534C2 DE2637534A DE2637534A DE2637534C2 DE 2637534 C2 DE2637534 C2 DE 2637534C2 DE 2637534 A DE2637534 A DE 2637534A DE 2637534 A DE2637534 A DE 2637534A DE 2637534 C2 DE2637534 C2 DE 2637534C2
- Authority
- DE
- Germany
- Prior art keywords
- catalyst
- general formula
- polymerization
- temperatures
- carried out
- 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
- 238000000034 method Methods 0.000 title claims description 16
- 125000004122 cyclic group Chemical group 0.000 title claims description 11
- 230000000379 polymerizing effect Effects 0.000 title claims description 3
- 238000006116 polymerization reaction Methods 0.000 claims description 19
- 229920000642 polymer Polymers 0.000 claims description 17
- 239000003054 catalyst Substances 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 7
- 239000002904 solvent Substances 0.000 claims description 7
- -1 Lewis acid compounds Chemical class 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 229910052782 aluminium Inorganic materials 0.000 claims description 4
- 229910052796 boron Inorganic materials 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- 239000002841 Lewis acid Substances 0.000 claims description 3
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 3
- 150000001450 anions Chemical group 0.000 claims description 3
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 230000015572 biosynthetic process Effects 0.000 claims description 3
- 229910052794 bromium Inorganic materials 0.000 claims description 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims 1
- 239000010452 phosphate Substances 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
- 238000002474 experimental method Methods 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 10
- 229910001220 stainless steel Inorganic materials 0.000 description 9
- 239000010935 stainless steel Substances 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 8
- 239000000460 chlorine Substances 0.000 description 7
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000000654 additive Substances 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 5
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 3
- 230000003197 catalytic effect Effects 0.000 description 3
- 241001233037 catfish Species 0.000 description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000003377 acid catalyst Substances 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 150000001805 chlorine compounds Chemical class 0.000 description 2
- CQYBWJYIKCZXCN-UHFFFAOYSA-N diethylaluminum Chemical compound CC[Al]CC CQYBWJYIKCZXCN-UHFFFAOYSA-N 0.000 description 2
- 239000012634 fragment Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000002902 organometallic compounds Chemical class 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000012719 thermal polymerization Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 238000004383 yellowing Methods 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- GTAVOQRDKZAAJP-UHFFFAOYSA-N diethylalumanylium;oxygen(2-) Chemical compound [O-2].CC[Al+]CC.CC[Al+]CC GTAVOQRDKZAAJP-UHFFFAOYSA-N 0.000 description 1
- YNLAOSYQHBDIKW-UHFFFAOYSA-M diethylaluminium chloride Chemical compound CC[Al](Cl)CC YNLAOSYQHBDIKW-UHFFFAOYSA-M 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 150000002366 halogen compounds Chemical class 0.000 description 1
- UBIJTWDKTYCPMQ-UHFFFAOYSA-N hexachlorophosphazene Chemical compound ClP1(Cl)=NP(Cl)(Cl)=NP(Cl)(Cl)=N1 UBIJTWDKTYCPMQ-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 230000000269 nucleophilic effect Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B21/00—Nitrogen; Compounds thereof
- C01B21/082—Compounds containing nitrogen and non-metals and optionally metals
- C01B21/097—Compounds containing nitrogen and non-metals and optionally metals containing phosphorus atoms
- C01B21/098—Phosphonitrilic dihalides; Polymers thereof
- C01B21/0986—Phosphonitrilic dichlorides; Polymers thereof
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B21/00—Nitrogen; Compounds thereof
- C01B21/082—Compounds containing nitrogen and non-metals and optionally metals
- C01B21/097—Compounds containing nitrogen and non-metals and optionally metals containing phosphorus atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Polyethers (AREA)
- Polyesters Or Polycarbonates (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US60680275A | 1975-08-22 | 1975-08-22 | |
| BE172213A BE848157A (fr) | 1975-08-22 | 1976-11-09 | Catalyse par les acides de lewis de la polymerisation des phosphazenes cycliques. |
| FR7636090A FR2372117A1 (fr) | 1975-08-22 | 1976-11-30 | Catalyse, a l'aide d'un acide de lewis, de la polymerisation de dichlorophosphazenes oligomeres |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2637534A1 DE2637534A1 (de) | 1977-03-03 |
| DE2637534C2 true DE2637534C2 (de) | 1984-08-09 |
Family
ID=27158614
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2637534A Expired DE2637534C2 (de) | 1975-08-22 | 1976-08-20 | Verfahren zum Polymerisieren von cyclischen Phosphazenen |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US4123503A (enExample) |
| JP (1) | JPS5244900A (enExample) |
| AU (1) | AU502967B2 (enExample) |
| CA (1) | CA1086024A (enExample) |
| DE (1) | DE2637534C2 (enExample) |
| FR (1) | FR2372117A1 (enExample) |
| GB (1) | GB1506835A (enExample) |
| NL (1) | NL173509C (enExample) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1109636A (en) * | 1977-04-18 | 1981-09-29 | Mark S. Prichard | Metal salt catalyzed polymerization of (npcl.sub.2) oligomers |
| EP0004877B1 (en) * | 1978-04-20 | 1982-05-12 | The Firestone Tire & Rubber Company | A process for thermally polymerizing cyclic phosphazenes |
| US4242316A (en) * | 1979-06-29 | 1980-12-30 | Standard Oil Company (Indiana) | Sulfamic acid as a catalyst for the polymerization of chlorocyclophosphazenes |
| US4226840A (en) * | 1979-09-19 | 1980-10-07 | The Firestone Tire & Rubber Company | Process for the polymerization of cyclic polyhalophosphazenes using a catalyst composition of boron trihalide and oxygenated phosphorus compounds |
| US4327064A (en) * | 1980-08-04 | 1982-04-27 | The Firestone Tire & Rubber Company | Solution polymerization of cyclic dichlorophosphazene oligomers in cycloaliphatic solvents |
| US4327063A (en) * | 1980-08-25 | 1982-04-27 | The Firestone Tire & Rubber Company | Method of purifying cyclic dichlorophosphazenes containing trace amounts of protic impurities |
| US4708858A (en) * | 1985-04-17 | 1987-11-24 | The Dow Chemical Company | Polymerization of cyclic dihalophosphazene oligomers |
| US4867957A (en) * | 1988-04-11 | 1989-09-19 | The United States Of America As Represented By The Secretary Of The Army | Process for making polyphosphazenes |
| US4870113A (en) * | 1988-12-23 | 1989-09-26 | Ethyl Corporation | Rigid polyphosphazene foam and process for making same |
| US5855809A (en) * | 1995-11-13 | 1999-01-05 | Arizona Board Of Regents | Electrochemically stable electrolytes |
| JP4184158B2 (ja) * | 2003-06-05 | 2008-11-19 | 旭化成ケミカルズ株式会社 | ホスホニトリル酸エステルの製造法 |
| FR2941455B1 (fr) * | 2009-01-29 | 2011-02-11 | Rhodia Operations | Procede de fabrication de composes comprenant des fonctions nitriles |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB883587A (en) * | 1957-09-06 | 1961-11-29 | Albright & Wilson Mfg Ltd | Production of phosphonitrilic polymers |
| US3917802A (en) * | 1973-04-11 | 1975-11-04 | Firestone Tire & Rubber Co | Molecular weight control in (NPCl{11 ){11 {11 polymerization |
| US4005171A (en) * | 1974-05-28 | 1977-01-25 | Horizons Incorporated, A Division Of Horizons Research Incorporated | Catalytic preparation of soluble poly(dichlorophosphazenes) |
| US4080432A (en) * | 1975-08-22 | 1978-03-21 | The Firestone Tire & Rubber Company | Dissolution of polydihalophosphazenes |
-
1976
- 1976-08-20 GB GB34860/76A patent/GB1506835A/en not_active Expired
- 1976-08-20 AU AU17043/76A patent/AU502967B2/en not_active Expired
- 1976-08-20 JP JP51099556A patent/JPS5244900A/ja active Granted
- 1976-08-20 CA CA259,560A patent/CA1086024A/en not_active Expired
- 1976-08-20 NL NLAANVRAGE7609253,A patent/NL173509C/xx not_active IP Right Cessation
- 1976-08-20 DE DE2637534A patent/DE2637534C2/de not_active Expired
- 1976-11-30 FR FR7636090A patent/FR2372117A1/fr active Granted
-
1977
- 1977-03-23 US US05/771,221 patent/US4123503A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| AU502967B2 (en) | 1979-08-16 |
| JPS5426239B2 (enExample) | 1979-09-03 |
| DE2637534A1 (de) | 1977-03-03 |
| CA1086024A (en) | 1980-09-23 |
| NL7609253A (nl) | 1977-02-24 |
| FR2372117A1 (fr) | 1978-06-23 |
| GB1506835A (en) | 1978-04-12 |
| JPS5244900A (en) | 1977-04-08 |
| US4123503A (en) | 1978-10-31 |
| AU1704376A (en) | 1978-02-23 |
| NL173509B (nl) | 1983-09-01 |
| NL173509C (nl) | 1984-02-01 |
| FR2372117B1 (enExample) | 1980-03-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2637534C2 (de) | Verfahren zum Polymerisieren von cyclischen Phosphazenen | |
| DE2135884C2 (de) | Verfahren zur Polymerisation von Äthylen oder dessen Gemischen mit α-Olefinen und/oder Diolefinen | |
| DE1958046C3 (de) | Verfahren zur Herstellung von Polymerisationskatalysatoren und deren Verwendung | |
| DE1958488B2 (de) | Polymerisationskatalysatoren, ihre Herstellung und Verwendung | |
| DE2624359A1 (de) | Verfahren zur herstellung von polyketonen | |
| DE2517142C2 (enExample) | ||
| DE2635895A1 (de) | Verfahren zur isolierung von polymeren | |
| EP0367106B1 (de) | Organosiloxanamin-Copolykondensate, Verfahren zu ihrer Herstellung und Verwendung (I) | |
| DE2745885C2 (de) | Verfahren zur Herstellung von Phosphazenpolymeren oder -copolymeren und deren Verwendung | |
| DE3425407C2 (de) | Katalysatorkomponente, Katalysator und Verfahren zur Polymerisation von Olefinen | |
| DE1595046C3 (de) | Verfahren zur Herstellung von PoIyarylenäthern | |
| EP0056229B1 (de) | Verfahren zur Herstellung von Trägerkatalysatoren für die Polymerisation von alpha-Olefinen | |
| DE1922017C3 (de) | Verfahren zur Herstellung von 2-Methylenglutarnitril durch Dimerisierung von Acrylnitril | |
| DE2829804A1 (de) | Verfahren zur herstellung von siloxanen und methylchlorid | |
| DE1542225A1 (de) | Polymerisationsverfahren | |
| DE2637535A1 (de) | Verfahren zur herstellung von loesungen von im wesentlichen linearen polydihalophosphazenen | |
| DE3422936C2 (enExample) | ||
| DE2646455A1 (de) | Verfahren zum isolieren von organozinnhalogeniden | |
| DE2822859C2 (de) | Verfahren zur Herstellung von acylgekoppelten Polymeren von chinongekoppelten Polyphenylenoxiden | |
| DE818425C (de) | Verfahren zur Herstellung linearer makromolekularer Aminosaeurepolykondensate aus Lactamen | |
| EP0602546B1 (de) | Verfahren zur Herstellung von 1-Amino-4-hydroxyanthrachinon | |
| DE1282616B (de) | Verfahren zur Herstellung teilweise reduzierter UEbergangsmetallbromide | |
| DE2262156A1 (de) | Verfahren zur herstellung von katalysatoren zur homopolymerisation von aethylen oder zur copolymerisation von aethylen mit alpha-olefinen | |
| DE1907242A1 (de) | Polymerisationskatalysator und kationische Polymerisation | |
| DE2816227C2 (enExample) |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OD | Request for examination | ||
| 8128 | New person/name/address of the agent |
Representative=s name: KOHLER, M., DIPL.-CHEM. DR.RER.NAT., PAT.-ANW., 80 |
|
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition | ||
| 8339 | Ceased/non-payment of the annual fee |