GB1430615A - Polyphenylene ethers - Google Patents
Polyphenylene ethersInfo
- Publication number
- GB1430615A GB1430615A GB5488873A GB5488873A GB1430615A GB 1430615 A GB1430615 A GB 1430615A GB 5488873 A GB5488873 A GB 5488873A GB 5488873 A GB5488873 A GB 5488873A GB 1430615 A GB1430615 A GB 1430615A
- Authority
- GB
- United Kingdom
- Prior art keywords
- phenol
- formula
- morpholine
- cupric
- xylenol
- 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
- 229920001955 polyphenylene ether Polymers 0.000 title abstract 3
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 abstract 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 5
- NXXYKOUNUYWIHA-UHFFFAOYSA-N 2,6-Dimethylphenol Chemical compound CC1=CC=CC(C)=C1O NXXYKOUNUYWIHA-UHFFFAOYSA-N 0.000 abstract 4
- 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
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 abstract 2
- QTMDXZNDVAMKGV-UHFFFAOYSA-L copper(ii) bromide Chemical compound [Cu+2].[Br-].[Br-] QTMDXZNDVAMKGV-UHFFFAOYSA-L 0.000 abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- KUFFULVDNCHOFZ-UHFFFAOYSA-N 2,4-xylenol Chemical compound CC1=CC=C(O)C(C)=C1 KUFFULVDNCHOFZ-UHFFFAOYSA-N 0.000 abstract 1
- KHRHTUNJTHWJPV-UHFFFAOYSA-N 2,6-dimethylphenol 4-methylphenol Chemical compound CC1=C(C(=CC=C1)C)O.C1=CC(=CC=C1O)C KHRHTUNJTHWJPV-UHFFFAOYSA-N 0.000 abstract 1
- ATGFTMUSEPZNJD-UHFFFAOYSA-N 2,6-diphenylphenol Chemical compound OC1=C(C=2C=CC=CC=2)C=CC=C1C1=CC=CC=C1 ATGFTMUSEPZNJD-UHFFFAOYSA-N 0.000 abstract 1
- 229910021590 Copper(II) bromide Inorganic materials 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000004743 Polypropylene Substances 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- 229960003280 cupric chloride Drugs 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 abstract 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 abstract 1
- 239000007789 gas Substances 0.000 abstract 1
- 229920000578 graft copolymer Polymers 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 150000002780 morpholines Chemical class 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- -1 polypropylene Polymers 0.000 abstract 1
- 229920001155 polypropylene Polymers 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
- 239000000243 solution Substances 0.000 abstract 1
- 239000000725 suspension Substances 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
- C08G65/46—Post-polymerisation treatment, e.g. recovery, purification, drying
-
- 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)
- Polyethers (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS808272A CS167575B1 (enExample) | 1972-11-28 | 1972-11-28 | |
| CS852972A CS159552B1 (enExample) | 1972-12-13 | 1972-12-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1430615A true GB1430615A (en) | 1976-03-31 |
Family
ID=25746557
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB5488873A Expired GB1430615A (en) | 1972-11-28 | 1973-11-27 | Polyphenylene ethers |
Country Status (6)
| Country | Link |
|---|---|
| JP (1) | JPS4998899A (enExample) |
| DD (1) | DD108564A1 (enExample) |
| DE (1) | DE2358729A1 (enExample) |
| FR (1) | FR2207951B3 (enExample) |
| GB (1) | GB1430615A (enExample) |
| NL (1) | NL7316296A (enExample) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4705843A (en) * | 1984-04-19 | 1987-11-10 | Bayer Aktiengesellschaft | Process for the production of substituted polyaryl ethers |
| EP0594249A3 (en) * | 1992-10-23 | 1994-09-07 | Enichem Spa | Process for preparing polyphenylene ethers with a low fines content |
| US8017716B2 (en) | 2009-07-01 | 2011-09-13 | Sabic Innovative Plastics Ip B.V. | Morpholine-substituted poly(arylene ether) and method for the preparation thereof |
| US8541505B2 (en) | 2008-09-30 | 2013-09-24 | Sabic Innovative Plastics Ip B.V. | Poly(arylene ether) composition with improved melt flow and method for the preparation thereof |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3224692A1 (de) * | 1982-07-02 | 1984-01-05 | Chemische Werke Hüls AG, 4370 Marl | Verfahren zur herstellung von polyphenylenoxiden |
| DE3313864A1 (de) * | 1983-04-16 | 1984-10-18 | Chemische Werke Hüls AG, 4370 Marl | Verfahren zur herstellung von polyphenylenoxiden |
-
1973
- 1973-11-26 DD DD17488873A patent/DD108564A1/xx unknown
- 1973-11-26 DE DE19732358729 patent/DE2358729A1/de active Pending
- 1973-11-27 GB GB5488873A patent/GB1430615A/en not_active Expired
- 1973-11-28 NL NL7316296A patent/NL7316296A/xx unknown
- 1973-11-28 FR FR7342274A patent/FR2207951B3/fr not_active Expired
- 1973-11-28 JP JP13393273A patent/JPS4998899A/ja active Pending
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4705843A (en) * | 1984-04-19 | 1987-11-10 | Bayer Aktiengesellschaft | Process for the production of substituted polyaryl ethers |
| EP0594249A3 (en) * | 1992-10-23 | 1994-09-07 | Enichem Spa | Process for preparing polyphenylene ethers with a low fines content |
| US8541505B2 (en) | 2008-09-30 | 2013-09-24 | Sabic Innovative Plastics Ip B.V. | Poly(arylene ether) composition with improved melt flow and method for the preparation thereof |
| US8017716B2 (en) | 2009-07-01 | 2011-09-13 | Sabic Innovative Plastics Ip B.V. | Morpholine-substituted poly(arylene ether) and method for the preparation thereof |
| US8124717B2 (en) | 2009-07-01 | 2012-02-28 | Sabic Innovative Plastics Ip B.V. | Morpholine-substituted poly(arylene ether) and method for the preparation thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS4998899A (enExample) | 1974-09-18 |
| NL7316296A (enExample) | 1974-05-30 |
| DD108564A1 (enExample) | 1974-09-20 |
| FR2207951B3 (enExample) | 1976-10-08 |
| DE2358729A1 (de) | 1974-06-06 |
| FR2207951A1 (enExample) | 1974-06-21 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |