GB1379028A - Process for preparing polyphenylene oxides - Google Patents
Process for preparing polyphenylene oxidesInfo
- Publication number
- GB1379028A GB1379028A GB5659571A GB5659571A GB1379028A GB 1379028 A GB1379028 A GB 1379028A GB 5659571 A GB5659571 A GB 5659571A GB 5659571 A GB5659571 A GB 5659571A GB 1379028 A GB1379028 A GB 1379028A
- Authority
- GB
- United Kingdom
- Prior art keywords
- cupric
- iodide
- cuprous
- polyphenylene oxides
- iodine
- 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
- 239000004721 Polyphenylene oxide Substances 0.000 title abstract 3
- 229920006380 polyphenylene oxide Polymers 0.000 title abstract 3
- 238000004519 manufacturing process Methods 0.000 title 1
- XTVVROIMIGLXTD-UHFFFAOYSA-N copper(II) nitrate Chemical compound [Cu+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O XTVVROIMIGLXTD-UHFFFAOYSA-N 0.000 abstract 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 abstract 3
- NXXYKOUNUYWIHA-UHFFFAOYSA-N 2,6-Dimethylphenol Chemical compound CC1=CC=CC(C)=C1O NXXYKOUNUYWIHA-UHFFFAOYSA-N 0.000 abstract 2
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 abstract 2
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 abstract 2
- 229910021595 Copper(I) iodide Inorganic materials 0.000 abstract 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 abstract 2
- LSXDOTMGLUJQCM-UHFFFAOYSA-M copper(i) iodide Chemical compound I[Cu] LSXDOTMGLUJQCM-UHFFFAOYSA-M 0.000 abstract 2
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 abstract 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 abstract 2
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 abstract 2
- -1 #-phenylethylamine Chemical compound 0.000 abstract 1
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 abstract 1
- LTHNHFOGQMKPOV-UHFFFAOYSA-N 2-ethylhexan-1-amine Chemical compound CCCCC(CC)CN LTHNHFOGQMKPOV-UHFFFAOYSA-N 0.000 abstract 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 abstract 1
- 239000005749 Copper compound Substances 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 abstract 1
- 150000001880 copper compounds Chemical class 0.000 abstract 1
- BERDEBHAJNAUOM-UHFFFAOYSA-N copper(I) oxide Inorganic materials [Cu]O[Cu] BERDEBHAJNAUOM-UHFFFAOYSA-N 0.000 abstract 1
- DOBRDRYODQBAMW-UHFFFAOYSA-N copper(i) cyanide Chemical compound [Cu+].N#[C-] DOBRDRYODQBAMW-UHFFFAOYSA-N 0.000 abstract 1
- 229940076286 cupric acetate Drugs 0.000 abstract 1
- 229960004643 cupric oxide Drugs 0.000 abstract 1
- KRFJLUBVMFXRPN-UHFFFAOYSA-N cuprous oxide Chemical compound [O-2].[Cu+].[Cu+] KRFJLUBVMFXRPN-UHFFFAOYSA-N 0.000 abstract 1
- 229940112669 cuprous oxide Drugs 0.000 abstract 1
- ZMMDPCMYTCRWFF-UHFFFAOYSA-J dicopper;carbonate;dihydroxide Chemical compound [OH-].[OH-].[Cu+2].[Cu+2].[O-]C([O-])=O ZMMDPCMYTCRWFF-UHFFFAOYSA-J 0.000 abstract 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 abstract 1
- 239000007789 gas Substances 0.000 abstract 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 abstract 1
- 229910000043 hydrogen iodide Inorganic materials 0.000 abstract 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 abstract 1
- 239000011630 iodine Substances 0.000 abstract 1
- 229910052740 iodine Inorganic materials 0.000 abstract 1
- 150000002497 iodine compounds Chemical class 0.000 abstract 1
- HVTICUPFWKNHNG-UHFFFAOYSA-N iodoethane Chemical compound CCI HVTICUPFWKNHNG-UHFFFAOYSA-N 0.000 abstract 1
- BMFVGAAISNGQNM-UHFFFAOYSA-N isopentylamine Chemical compound CC(C)CCN BMFVGAAISNGQNM-UHFFFAOYSA-N 0.000 abstract 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 230000001590 oxidative effect Effects 0.000 abstract 1
- DPBLXKKOBLCELK-UHFFFAOYSA-N pentan-1-amine Chemical compound CCCCCN DPBLXKKOBLCELK-UHFFFAOYSA-N 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 150000003335 secondary amines Chemical class 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 229910021653 sulphate ion Inorganic materials 0.000 abstract 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- C08G65/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
- C08G65/44—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols by oxidation of phenols
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyethers (AREA)
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7143662A FR2116555B1 (enExample) | 1970-12-07 | 1971-12-06 | |
| CA129,470A CA944897A (en) | 1970-12-07 | 1971-12-06 | Process for preparing polyphenylene oxides |
| DE2160419A DE2160419C3 (de) | 1970-12-07 | 1971-12-06 | Verfahren zur Herstellung von PoIyphenylenoxiden |
| GB5659571A GB1379028A (en) | 1970-12-07 | 1971-12-06 | Process for preparing polyphenylene oxides |
| NL7116787.A NL166483C (nl) | 1970-12-07 | 1971-12-07 | Werkwijze ter bereiding van polyfenyleenoxyden. |
| BE776339A BE776339A (fr) | 1970-12-07 | 1971-12-07 | Procede de preparation d'oxydes de polyphenylene |
| US05/639,141 US4067851A (en) | 1970-11-16 | 1975-12-09 | Process for preparing polyphenylene oxides |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10763770A JPS4842480B1 (enExample) | 1970-12-07 | 1970-12-07 | |
| GB5659571A GB1379028A (en) | 1970-12-07 | 1971-12-06 | Process for preparing polyphenylene oxides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1379028A true GB1379028A (en) | 1975-01-02 |
Family
ID=26267632
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB5659571A Expired GB1379028A (en) | 1970-11-16 | 1971-12-06 | Process for preparing polyphenylene oxides |
Country Status (6)
| Country | Link |
|---|---|
| BE (1) | BE776339A (enExample) |
| CA (1) | CA944897A (enExample) |
| DE (1) | DE2160419C3 (enExample) |
| FR (1) | FR2116555B1 (enExample) |
| GB (1) | GB1379028A (enExample) |
| NL (1) | NL166483C (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0045395A1 (de) * | 1980-08-02 | 1982-02-10 | BASF Aktiengesellschaft | Verfahren zur Herstellung von Polyphenylenäthern |
| RU2806582C1 (ru) * | 2023-01-30 | 2023-11-01 | Акционерное общество "Научно-производственное объединение "ГЕЛИЙМАШ" (АО "НПО "ГЕЛИЙМАШ") | Способ получения поли-2,6-диметил-1,4-фениленоксида |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4067851A (en) | 1970-11-16 | 1978-01-10 | Mitsubishi Gas Chemical Company, Inc. | Process for preparing polyphenylene oxides |
| DE3033813A1 (de) * | 1980-09-09 | 1982-04-22 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von polyphenylenaethern |
| DE3035599A1 (de) * | 1980-09-20 | 1982-05-06 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von polyphenylenaethern |
| DE3042149A1 (de) * | 1980-11-08 | 1982-06-24 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von polyphenylenaethern |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3344116A (en) * | 1965-03-29 | 1967-09-26 | Gen Electric | Process for the formation of polyphenylene oxides |
-
1971
- 1971-12-06 CA CA129,470A patent/CA944897A/en not_active Expired
- 1971-12-06 DE DE2160419A patent/DE2160419C3/de not_active Expired
- 1971-12-06 FR FR7143662A patent/FR2116555B1/fr not_active Expired
- 1971-12-06 GB GB5659571A patent/GB1379028A/en not_active Expired
- 1971-12-07 NL NL7116787.A patent/NL166483C/xx not_active IP Right Cessation
- 1971-12-07 BE BE776339A patent/BE776339A/xx not_active IP Right Cessation
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0045395A1 (de) * | 1980-08-02 | 1982-02-10 | BASF Aktiengesellschaft | Verfahren zur Herstellung von Polyphenylenäthern |
| RU2806582C1 (ru) * | 2023-01-30 | 2023-11-01 | Акционерное общество "Научно-производственное объединение "ГЕЛИЙМАШ" (АО "НПО "ГЕЛИЙМАШ") | Способ получения поли-2,6-диметил-1,4-фениленоксида |
Also Published As
| Publication number | Publication date |
|---|---|
| BE776339A (fr) | 1972-04-04 |
| DE2160419C3 (de) | 1974-04-04 |
| FR2116555B1 (enExample) | 1976-04-02 |
| NL166483C (nl) | 1981-08-17 |
| CA944897A (en) | 1974-04-02 |
| FR2116555A1 (enExample) | 1972-07-13 |
| DE2160419A1 (de) | 1972-07-13 |
| NL7116787A (enExample) | 1972-06-09 |
| DE2160419B2 (de) | 1973-09-13 |
| NL166483B (nl) | 1981-03-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |