CN1340553A - 一种新的取代酚的氧化聚合物 - Google Patents
一种新的取代酚的氧化聚合物 Download PDFInfo
- Publication number
- CN1340553A CN1340553A CN01135735A CN01135735A CN1340553A CN 1340553 A CN1340553 A CN 1340553A CN 01135735 A CN01135735 A CN 01135735A CN 01135735 A CN01135735 A CN 01135735A CN 1340553 A CN1340553 A CN 1340553A
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- CN
- China
- Prior art keywords
- carbon atom
- substituted
- expression
- oxypolymer
- unsubstituted
- 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.)
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Classifications
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- 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
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Polyethers (AREA)
Abstract
Description
单体 | 催化剂(对于单体的金属部分mol%) | 反应时间(h) | 单体转化率(%) | 聚合物产率(%) | 溶解性(oDCB/150℃) | Mn | Mw | Tm(℃) | Hm(J/g) | |
(oDCB/140℃) | ||||||||||
实施例1 | 2-正十八酚 | Cu(tacn) (5) | 48 | 98 | 90 | 溶解 | 5400 | 10900 | 39 | 60 |
实施例2 | 2-正十八酚 | Cu(tacn) (5) | 24 | 94 | 73 | 溶解 | 4500 | 8500 | 40 | 70 |
实施例3 | 2-正十八酚 | Cu(tacn) (5) | 240 | 100 | 93 | 溶解 | 13500 | 55500 | 38 | 60 |
实施例4 | 2-正十八酚 | Cu(tmed) (5) | 24 | 100 | 90 | 溶解 | 4100 | 7100 | 39 | 59 |
实施例5 | 2-正十八酚 | CuCl/Py(5) | 29 | 100 | 85 | 溶解 | 2900 | 4500 | 40 | 64 |
实施例6 | 2-正十八酚 | Fe(salen) (5) | 21 | 98 | 69 | 部分不溶解 | 3400* | 6300* | 31 | 41 |
实施例7 | 2-正十二酚 | Cu(tacn) (5) | 48 | 98 | 91 | 溶解 | 7200** | 19800** | -32 | 9 |
实施例8 | 2-正十五酚 | Cu(tacn) (5) | 48 | 98 | 90 | 溶解 | 4100 | 9700 | 17 | 47 |
实施例9 | 2-正二十二酚 | Cu(tacn) (5) | 48 | 99 | 89 | 溶解 | 7300 | 12800 | 59 | 81 |
实施例10 | 3-正十五酚 | Cu(tacn) (0.5) | 192 | 47 | 23 | 溶解 | 4200 | 6900 | 19 | 40 |
实施例11 | 4-正十八酚 | Cu(tacn) (5) | 28 | 98 | 77 | 溶解 | 2600 | 3200 | 50 | 43 |
实施例12 | 2-(2-十八酚) | Cu(tacn) (5) | 52 | 97 | 88 | 溶解 | 4200 | 6900 | 18 | 38 |
单体(1)(mol%) | 单体(2)(mol%) | 单体(1)转化率(%) | 单体(2)转化率(%) | 聚合物产率(%) | 溶解性(oDCB/150℃) | Mn | Mw | Tm(℃) | Hm(J/g) | |
(oDCB/140℃) | ||||||||||
实施例13 | 2-正十八酚(25) | 2-正十五酚(75) | 99 | 99 | 92 | 溶解 | 5700 | 18100 | 21 | 44 |
实施例14 | 2-正十八酚(50) | 2-正十五酚(50) | 99 | 98 | 94 | 溶解 | 6000 | 19000 | 26 | 51 |
实施例15 | 2-正十八酚(75) | 2-正十五酚(25) | 98 | 98 | 85 | 溶解 | 5900 | 12700 | 33 | 55 |
实施例16 | 2-正十八酚(75) | 2-正十二酚(25) | 99 | 98 | 72 | 溶解 | 5500 | 11900 | 31 | 53 |
实施例17 | 2-正十八酚(75) | 2-正二十二酚(25) | 98 | 98 | 81 | 溶解 | 6000 | 11400 | 42 | 78 |
实施例18 | 2-正十八酚(50) | 2-甲酚(50) | 98 | 99 | 83 | 溶解 | 9800 | 17200 | 27 | 38 |
实施例19 | 2-正十八酚(75) | 2-甲酚(25) | 99 | 100 | 87 | 溶解 | 3600 | 9600 | 34 | 58 |
单体 | 反应时间(h) | 单体转化率(%) | 聚合物产率(%) | 溶解性(oDCB/150℃) | Mn | Mw | Tm’(℃) | Hm’(J/g) | Tm(℃) | Hm(J/g) | |
(oDCB/140℃) | |||||||||||
实施例20 | 2-正十八烷基-6-甲酚 | 24 | 100 | 89 | 溶解 | 15900 | 27900 | 40 | 47 | 34 | 49 |
实施例21 | 2-(2-十八烷基)-6-甲酚 | 24 | 99 | 79 | 溶解 | 3300 | 9100 | 9 | 30 | 12 | 27 |
实施例22 | 2,6-二正十八酚 | 29 | 100 | 91 | 溶解 | 6400 | 14600 | 73 | 106 | 66 | 98 |
单体 | 反应时间(h) | 单体转化率(%) | 聚合物产率(%) | 溶解性(oDCB/150℃) | Mn | Mw | Tm’(℃) | Hm’(J/g) | Tm(℃) | Hm(J/g) | |
(oDCB/140℃) | |||||||||||
比较例1 | 2-正壬酚 | 48 | 99 | 78 | 溶解 | 8200 | 17100 | N.D. | N.D. | N.D. | N.D. |
Claims (20)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2000216485A JP4827280B2 (ja) | 2000-07-17 | 2000-07-17 | 新規な2,6−ジ置換フェノール酸化重合体 |
JP216482/2000 | 2000-07-17 | ||
JP2000216482A JP4783494B2 (ja) | 2000-07-17 | 2000-07-17 | 新規な置換フェノール酸化重合体 |
JP216485/2000 | 2000-07-17 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1340553A true CN1340553A (zh) | 2002-03-20 |
CN1185280C CN1185280C (zh) | 2005-01-19 |
Family
ID=26596171
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB011357355A Expired - Fee Related CN1185280C (zh) | 2000-07-17 | 2001-07-17 | 一种新的取代酚的氧化聚合物 |
Country Status (3)
Country | Link |
---|---|
US (1) | US6576800B2 (zh) |
CN (1) | CN1185280C (zh) |
DE (1) | DE10134627A1 (zh) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW572882B (en) * | 2001-10-17 | 2004-01-21 | Mitsubishi Gas Chemical Co | Bifunctional biphenyl and process for producing bifunctional phenylene ether oligomer compound using the same |
JP4471073B2 (ja) * | 2003-07-02 | 2010-06-02 | 三菱瓦斯化学株式会社 | 2官能性フェニレンエーテルオリゴマー体の製造法 |
JP2008509272A (ja) * | 2004-08-09 | 2008-03-27 | スティヒティング エネルギーオンダーゾーク セントラム ネーデルランド | プロトン伝導性コポリマー |
US10995182B2 (en) | 2018-04-30 | 2021-05-04 | Shpp Global Technologies B.V. | Phenylene ether oligomer, curable composition comprising the phenylene ether oligomer, and thermoset composition derived therefrom |
CN111793203B (zh) * | 2020-07-22 | 2022-12-27 | 广东省石油与精细化工研究院 | 一种聚苯醚及其合成方法 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5853948A (ja) * | 1981-09-28 | 1983-03-30 | Kanegafuchi Chem Ind Co Ltd | 耐熱性樹脂組成物 |
JP2514051B2 (ja) * | 1986-10-31 | 1996-07-10 | 住友化学工業株式会社 | 熱可塑性樹脂組成物 |
JP3028561B2 (ja) * | 1990-07-10 | 2000-04-04 | 宇部サイコン株式会社 | ポリフェニレンエーテル組成物 |
DE69124481T2 (de) * | 1990-11-29 | 1997-06-12 | Mitsubishi Chem Corp | Polyhydroxyphenylenetherharzzusammensetzung und Verfahren zu ihrer Herstellung |
US5037943A (en) * | 1990-12-18 | 1991-08-06 | General Electric Co. | Polyphenylene ether process and resin composition |
DE69329136T2 (de) * | 1992-10-14 | 2001-06-07 | Mitsubishi Chem Corp | Verfahren zur Herstellung einer thermoplastischen Harzzusammensetzung |
TW377367B (en) * | 1994-06-21 | 1999-12-21 | Asahi Kasei Corp | Aromatic polycarbonate-styrene polymer resin composition |
-
2001
- 2001-07-17 CN CNB011357355A patent/CN1185280C/zh not_active Expired - Fee Related
- 2001-07-17 US US09/905,978 patent/US6576800B2/en not_active Expired - Fee Related
- 2001-07-17 DE DE10134627A patent/DE10134627A1/de not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
US20020028907A1 (en) | 2002-03-07 |
CN1185280C (zh) | 2005-01-19 |
US6576800B2 (en) | 2003-06-10 |
DE10134627A1 (de) | 2002-03-07 |
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Effective date of registration: 20091127 Address after: Tokyo Co-patentee after: Sumitomo Chemical Co., Ltd. Patentee after: Comprehensive Research Institute of industrial technology of independent administrative legal person Address before: Tokyo Co-patentee before: Chemical technology strategy promoter Patentee before: Comprehensive Research Institute of industrial technology of independent administrative legal person |
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CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20050119 Termination date: 20150717 |
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