JPWO2021153178A5 - - Google Patents
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- Publication number
- JPWO2021153178A5 JPWO2021153178A5 JP2021574577A JP2021574577A JPWO2021153178A5 JP WO2021153178 A5 JPWO2021153178 A5 JP WO2021153178A5 JP 2021574577 A JP2021574577 A JP 2021574577A JP 2021574577 A JP2021574577 A JP 2021574577A JP WO2021153178 A5 JPWO2021153178 A5 JP WO2021153178A5
- Authority
- JP
- Japan
- Prior art keywords
- bis
- hydroxyphenyl
- bisphenol
- diglycidyl ether
- dihydric phenol
- 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.)
- Granted
Links
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 10
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 10
- 239000003822 epoxy resin Substances 0.000 description 8
- 229920000647 polyepoxide Polymers 0.000 description 8
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 5
- 239000004593 Epoxy Substances 0.000 description 5
- 230000001588 bifunctional effect Effects 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 4
- -1 phenol compound Chemical class 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- HCNHNBLSNVSJTJ-UHFFFAOYSA-N 1,1-Bis(4-hydroxyphenyl)ethane Chemical compound C=1C=C(O)C=CC=1C(C)C1=CC=C(O)C=C1 HCNHNBLSNVSJTJ-UHFFFAOYSA-N 0.000 description 1
- DIQCVUZVAPYLCM-UHFFFAOYSA-N 2-[[2-chloro-4-(oxiran-2-ylmethoxy)phenoxy]methyl]oxirane Chemical compound C=1C=C(OCC2OC2)C(Cl)=CC=1OCC1CO1 DIQCVUZVAPYLCM-UHFFFAOYSA-N 0.000 description 1
- LRVJEADXJYKWPQ-UHFFFAOYSA-N 2-[[2-methyl-4-(oxiran-2-ylmethoxy)phenoxy]methyl]oxirane Chemical compound C=1C=C(OCC2OC2)C(C)=CC=1OCC1CO1 LRVJEADXJYKWPQ-UHFFFAOYSA-N 0.000 description 1
- AGXAFZNONAXBOS-UHFFFAOYSA-N 2-[[3-(oxiran-2-ylmethyl)phenyl]methyl]oxirane Chemical compound C=1C=CC(CC2OC2)=CC=1CC1CO1 AGXAFZNONAXBOS-UHFFFAOYSA-N 0.000 description 1
- FSYPIGPPWAJCJG-UHFFFAOYSA-N 2-[[4-(oxiran-2-ylmethoxy)phenoxy]methyl]oxirane Chemical compound C1OC1COC(C=C1)=CC=C1OCC1CO1 FSYPIGPPWAJCJG-UHFFFAOYSA-N 0.000 description 1
- ZDRSNHRWLQQICP-UHFFFAOYSA-N 2-tert-butyl-4-[2-(3-tert-butyl-4-hydroxyphenyl)propan-2-yl]phenol Chemical compound C1=C(O)C(C(C)(C)C)=CC(C(C)(C)C=2C=C(C(O)=CC=2)C(C)(C)C)=C1 ZDRSNHRWLQQICP-UHFFFAOYSA-N 0.000 description 1
- VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 description 1
- YMTYZTXUZLQUSF-UHFFFAOYSA-N 3,3'-Dimethylbisphenol A Chemical compound C1=C(O)C(C)=CC(C(C)(C)C=2C=C(C)C(O)=CC=2)=C1 YMTYZTXUZLQUSF-UHFFFAOYSA-N 0.000 description 1
- RXNYJUSEXLAVNQ-UHFFFAOYSA-N 4,4'-Dihydroxybenzophenone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=C(O)C=C1 RXNYJUSEXLAVNQ-UHFFFAOYSA-N 0.000 description 1
- NZGQHKSLKRFZFL-UHFFFAOYSA-N 4-(4-hydroxyphenoxy)phenol Chemical compound C1=CC(O)=CC=C1OC1=CC=C(O)C=C1 NZGQHKSLKRFZFL-UHFFFAOYSA-N 0.000 description 1
- BATCUENAARTUKW-UHFFFAOYSA-N 4-[(4-hydroxyphenyl)-diphenylmethyl]phenol Chemical compound C1=CC(O)=CC=C1C(C=1C=CC(O)=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 BATCUENAARTUKW-UHFFFAOYSA-N 0.000 description 1
- UMPGNGRIGSEMTC-UHFFFAOYSA-N 4-[1-(4-hydroxyphenyl)-3,3,5-trimethylcyclohexyl]phenol Chemical compound C1C(C)CC(C)(C)CC1(C=1C=CC(O)=CC=1)C1=CC=C(O)C=C1 UMPGNGRIGSEMTC-UHFFFAOYSA-N 0.000 description 1
- KOWHWSRFLBFYRR-UHFFFAOYSA-N 4-[1-[3-[2-(4-hydroxyphenyl)propyl]phenyl]propan-2-yl]phenol Chemical compound C=1C=C(O)C=CC=1C(C)CC(C=1)=CC=CC=1CC(C)C1=CC=C(O)C=C1 KOWHWSRFLBFYRR-UHFFFAOYSA-N 0.000 description 1
- OKWDECPYZNNVPP-UHFFFAOYSA-N 4-[1-[4-[2-(4-hydroxyphenyl)propyl]phenyl]propan-2-yl]phenol Chemical compound C=1C=C(O)C=CC=1C(C)CC(C=C1)=CC=C1CC(C)C1=CC=C(O)C=C1 OKWDECPYZNNVPP-UHFFFAOYSA-N 0.000 description 1
- BKTRENAPTCBBFA-UHFFFAOYSA-N 4-[2-(4-hydroxy-3-phenylphenyl)propan-2-yl]-2-phenylphenol Chemical compound C=1C=C(O)C(C=2C=CC=CC=2)=CC=1C(C)(C)C(C=1)=CC=C(O)C=1C1=CC=CC=C1 BKTRENAPTCBBFA-UHFFFAOYSA-N 0.000 description 1
- BDUZRCOGHMYBQN-UHFFFAOYSA-N 4-[3-(4-hydroxyphenyl)-15,18,21-trioxahexacyclo[11.9.0.02,10.04,9.014,16.020,22]docosa-1(13),2(10),4,6,8,11-hexaen-3-yl]phenol Chemical compound OC1=CC=C(C=C1)C1(C2=CC=CC=C2C2=CC=C3C(=C12)C1C(COCC2C3O2)O1)C1=CC=C(C=C1)O BDUZRCOGHMYBQN-UHFFFAOYSA-N 0.000 description 1
- YWFPGFJLYRKYJZ-UHFFFAOYSA-N 9,9-bis(4-hydroxyphenyl)fluorene Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C2=CC=CC=C21 YWFPGFJLYRKYJZ-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- VOWWYDCFAISREI-UHFFFAOYSA-N Bisphenol AP Chemical compound C=1C=C(O)C=CC=1C(C=1C=CC(O)=CC=1)(C)C1=CC=CC=C1 VOWWYDCFAISREI-UHFFFAOYSA-N 0.000 description 1
- HTVITOHKHWFJKO-UHFFFAOYSA-N Bisphenol B Chemical compound C=1C=C(O)C=CC=1C(C)(CC)C1=CC=C(O)C=C1 HTVITOHKHWFJKO-UHFFFAOYSA-N 0.000 description 1
- SDDLEVPIDBLVHC-UHFFFAOYSA-N Bisphenol Z Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)CCCCC1 SDDLEVPIDBLVHC-UHFFFAOYSA-N 0.000 description 1
- ALEHMZVXZAOMNG-UHFFFAOYSA-N OC12C(C3=CC=C(C=C3C=C1)O)C1C(COCC3C2O3)O1 Chemical compound OC12C(C3=CC=C(C=C3C=C1)O)C1C(COCC3C2O3)O1 ALEHMZVXZAOMNG-UHFFFAOYSA-N 0.000 description 1
- VCCBEIPGXKNHFW-UHFFFAOYSA-N biphenyl-4,4'-diol Chemical group C1=CC(O)=CC=C1C1=CC=C(O)C=C1 VCCBEIPGXKNHFW-UHFFFAOYSA-N 0.000 description 1
- ZFVMWEVVKGLCIJ-UHFFFAOYSA-N bisphenol AF Chemical compound C1=CC(O)=CC=C1C(C(F)(F)F)(C(F)(F)F)C1=CC=C(O)C=C1 ZFVMWEVVKGLCIJ-UHFFFAOYSA-N 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- 229960001755 resorcinol Drugs 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2020014084 | 2020-01-30 | ||
| JP2020014084 | 2020-01-30 | ||
| PCT/JP2021/000302 WO2021153178A1 (ja) | 2020-01-30 | 2021-01-07 | 非晶性エポキシ系繊維、繊維構造体および成形体 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JPWO2021153178A1 JPWO2021153178A1 (https=) | 2021-08-05 |
| JPWO2021153178A5 true JPWO2021153178A5 (https=) | 2022-09-15 |
| JP7374230B2 JP7374230B2 (ja) | 2023-11-06 |
Family
ID=77078365
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021574577A Active JP7374230B2 (ja) | 2020-01-30 | 2021-01-07 | 非晶性エポキシ系繊維、繊維構造体および成形体 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20220363810A1 (https=) |
| EP (1) | EP4098785A4 (https=) |
| JP (1) | JP7374230B2 (https=) |
| CN (1) | CN115038828B (https=) |
| TW (1) | TWI862775B (https=) |
| WO (1) | WO2021153178A1 (https=) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20240019322A (ko) * | 2021-06-24 | 2024-02-14 | 주식회사 쿠라레 | 섬유 구조체, 가교 성형체, 및 가교 성형체의 제조 방법 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS519408B1 (https=) * | 1971-06-01 | 1976-03-26 | ||
| JPS4925219A (https=) * | 1972-05-22 | 1974-03-06 | ||
| US4207408A (en) * | 1972-05-22 | 1980-06-10 | The Carborundum Company | High tenacity phenolic resin fibers |
| JP2580892B2 (ja) * | 1991-06-28 | 1997-02-12 | 日立化成工業株式会社 | エポキシ繊維 |
| KR100474798B1 (ko) * | 2002-12-27 | 2005-03-10 | 주식회사 효성 | 고무 또는 폴리비닐 클로라이드에 대한 접착력이 우수한폴리에스테르 섬유 및 이의 제조방법 |
| ATE384150T1 (de) | 2005-03-22 | 2008-02-15 | Ems Chemie Ag | Aus einem polyhydroxyether enthaltenden rohstoff gesponnenes thermoplastisches fasermaterial, verfahren zu seiner herstellung und verwendungen dafür |
| US20080055724A1 (en) * | 2006-08-30 | 2008-03-06 | 3M Innovative Properties Company | Optical devices containing birefringent polymer fibers |
| CN102362021B (zh) * | 2009-03-26 | 2014-04-23 | 株式会社可乐丽 | 非晶性聚醚酰亚胺类纤维和耐热性布帛 |
| JP5860798B2 (ja) | 2012-12-07 | 2016-02-16 | 住江織物株式会社 | フェノキシ樹脂製糸の製造方法 |
| CN104032409B (zh) * | 2014-06-05 | 2016-06-15 | 哈尔滨工业大学 | 热固/热塑核壳结构的形状记忆复合纤维及其制备方法 |
-
2021
- 2021-01-07 CN CN202180011813.9A patent/CN115038828B/zh active Active
- 2021-01-07 EP EP21748430.2A patent/EP4098785A4/en active Pending
- 2021-01-07 WO PCT/JP2021/000302 patent/WO2021153178A1/ja not_active Ceased
- 2021-01-07 JP JP2021574577A patent/JP7374230B2/ja active Active
- 2021-01-15 TW TW110101564A patent/TWI862775B/zh active
-
2022
- 2022-07-22 US US17/870,982 patent/US20220363810A1/en active Pending
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