JP2000264953A5 - - Google Patents
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- Publication number
- JP2000264953A5 JP2000264953A5 JP1999065706A JP6570699A JP2000264953A5 JP 2000264953 A5 JP2000264953 A5 JP 2000264953A5 JP 1999065706 A JP1999065706 A JP 1999065706A JP 6570699 A JP6570699 A JP 6570699A JP 2000264953 A5 JP2000264953 A5 JP 2000264953A5
- Authority
- JP
- Japan
- Prior art keywords
- epoxy resin
- cross
- mmol
- reaction
- mca
- 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.)
- Pending
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- 239000003822 epoxy resin Substances 0.000 claims description 46
- 229920000647 polyepoxide Polymers 0.000 claims description 46
- 239000000203 mixture Substances 0.000 claims description 39
- 239000003431 cross linking reagent Substances 0.000 claims description 19
- 239000003054 catalyst Substances 0.000 claims description 12
- VTJUKNSKBAOEHE-UHFFFAOYSA-N calixarene Chemical class COC(=O)COC1=C(CC=2C(=C(CC=3C(=C(C4)C=C(C=3)C(C)(C)C)OCC(=O)OC)C=C(C=2)C(C)(C)C)OCC(=O)OC)C=C(C(C)(C)C)C=C1CC1=C(OCC(=O)OC)C4=CC(C(C)(C)C)=C1 VTJUKNSKBAOEHE-UHFFFAOYSA-N 0.000 claims description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 3
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims 1
- 230000026731 phosphorylation Effects 0.000 claims 1
- 238000006366 phosphorylation reaction Methods 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 description 40
- 238000004132 cross linking Methods 0.000 description 27
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 16
- 238000010438 heat treatment Methods 0.000 description 16
- 239000002904 solvent Substances 0.000 description 11
- 150000001361 allenes Chemical class 0.000 description 10
- 125000003700 epoxy group Chemical group 0.000 description 9
- 238000002329 infrared spectrum Methods 0.000 description 9
- -1 resorcin allenes Chemical class 0.000 description 8
- 229960001755 resorcinol Drugs 0.000 description 7
- 229930185605 Bisphenol Natural products 0.000 description 6
- 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 6
- 230000009477 glass transition Effects 0.000 description 6
- RKHXQBLJXBGEKF-UHFFFAOYSA-M tetrabutylphosphanium;bromide Chemical compound [Br-].CCCC[P+](CCCC)(CCCC)CCCC RKHXQBLJXBGEKF-UHFFFAOYSA-M 0.000 description 6
- 238000010586 diagram Methods 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 229920003986 novolac Polymers 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 101100207323 Arabidopsis thaliana TPPC gene Proteins 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 125000004185 ester group Chemical group 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- 229920000858 Cyclodextrin Polymers 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 150000003983 crown ethers Chemical class 0.000 description 1
- 150000001923 cyclic compounds Chemical class 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 125000002270 phosphoric acid ester group Chemical group 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- BRKFQVAOMSWFDU-UHFFFAOYSA-M tetraphenylphosphanium;bromide Chemical compound [Br-].C1=CC=CC=C1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 BRKFQVAOMSWFDU-UHFFFAOYSA-M 0.000 description 1
Images
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11065706A JP2000264953A (ja) | 1999-03-11 | 1999-03-11 | エポキシ樹脂硬化性組成物 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11065706A JP2000264953A (ja) | 1999-03-11 | 1999-03-11 | エポキシ樹脂硬化性組成物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2000264953A JP2000264953A (ja) | 2000-09-26 |
| JP2000264953A5 true JP2000264953A5 (https=) | 2005-05-19 |
Family
ID=13294744
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11065706A Pending JP2000264953A (ja) | 1999-03-11 | 1999-03-11 | エポキシ樹脂硬化性組成物 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2000264953A (https=) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7037638B1 (en) * | 2000-05-31 | 2006-05-02 | International Business Machines Corporation | High sensitivity crosslinkable photoresist composition, based on soluble, film forming dendrimeric calix[4] arene compositions method and for use thereof |
| DE102007035734A1 (de) | 2006-08-29 | 2008-03-20 | Ivoclar Vivadent Ag | Dentalmaterialien mit geringem Polymerisationsschrumpf |
| JP5750777B2 (ja) * | 2009-04-24 | 2015-07-22 | 日立化成株式会社 | カリックスアレーン誘導体、カリックスアレーン誘導体の製造方法、エポキシ樹脂用硬化剤、エポキシ樹脂組成物及び電子部品装置 |
| JP5584878B2 (ja) * | 2010-02-10 | 2014-09-10 | 学校法人神奈川大学 | 重合性低屈折ポリマーの製造方法、及び光学材料の製造方法 |
| JP6156818B2 (ja) * | 2013-04-30 | 2017-07-05 | 学校法人 関西大学 | 高分子および当該高分子の製造方法 |
| CN108864654B (zh) * | 2017-05-10 | 2023-07-14 | 味之素株式会社 | 树脂组合物层 |
| CN111849344B (zh) * | 2020-08-17 | 2021-08-13 | 山东世安化工有限公司 | 一种环保建筑防火涂料及其制备方法 |
| CN118599425B (zh) * | 2024-06-04 | 2025-10-21 | 江苏苏博特新材料股份有限公司 | 一种自修复抗辐射涂层涂料、抗辐射涂层及其制备方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02123126A (ja) * | 1988-11-01 | 1990-05-10 | Wakayama Pref Gov | 熱硬化性樹脂の製造方法 |
| JPH06136341A (ja) * | 1992-10-22 | 1994-05-17 | Toray Ind Inc | 接着剤 |
| JPH07292050A (ja) * | 1994-04-21 | 1995-11-07 | Daihachi Chem Ind Co Ltd | 含燐ノボラック型フェノール樹脂及び難燃性樹脂組成物 |
| JPH0834835A (ja) * | 1994-07-26 | 1996-02-06 | Hitachi Chem Co Ltd | エポキシ樹脂組成物及びその硬化物 |
| JP3596630B2 (ja) * | 1995-02-28 | 2004-12-02 | 大日本インキ化学工業株式会社 | 硬化性エポキシ樹脂組成物 |
-
1999
- 1999-03-11 JP JP11065706A patent/JP2000264953A/ja active Pending
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