TWI853070B - 樹脂原料用組成物 - Google Patents
樹脂原料用組成物 Download PDFInfo
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- TWI853070B TWI853070B TW109128088A TW109128088A TWI853070B TW I853070 B TWI853070 B TW I853070B TW 109128088 A TW109128088 A TW 109128088A TW 109128088 A TW109128088 A TW 109128088A TW I853070 B TWI853070 B TW I853070B
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- 239000000203 mixture Substances 0.000 title claims abstract description 65
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- BAQCVMJWHJZMCA-UHFFFAOYSA-N [2,3,6-trimethyl-4-[2,3,5-trimethyl-4-(naphthalene-1-carbonyloxy)phenyl]phenyl] naphthalene-1-carboxylate Chemical compound CC1=CC(C(C=C2C)=C(C)C(C)=C2OC(C2=CC=CC3=CC=CC=C23)=O)=C(C)C(C)=C1OC(C1=CC=CC2=CC=CC=C12)=O BAQCVMJWHJZMCA-UHFFFAOYSA-N 0.000 description 1
- RPJNGJGIXYEMNF-UHFFFAOYSA-N [4-(4-acetyloxy-2,3,5-trimethylphenyl)-2,3,6-trimethylphenyl] acetate Chemical compound CC1=C(C)C(OC(=O)C)=C(C)C=C1C1=CC(C)=C(OC(C)=O)C(C)=C1C RPJNGJGIXYEMNF-UHFFFAOYSA-N 0.000 description 1
- QHGDBCLREIFZGR-UHFFFAOYSA-N [4-(4-butanoyloxy-2,3,5-trimethylphenyl)-2,3,6-trimethylphenyl] butanoate Chemical compound CCCC(OC(C(C)=C1)=C(C)C(C)=C1C(C=C1C)=C(C)C(C)=C1OC(CCC)=O)=O QHGDBCLREIFZGR-UHFFFAOYSA-N 0.000 description 1
- OXIKYYJDTWKERT-UHFFFAOYSA-N [4-(aminomethyl)cyclohexyl]methanamine Chemical compound NCC1CCC(CN)CC1 OXIKYYJDTWKERT-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000005456 alcohol based solvent Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000001346 alkyl aryl ethers Chemical class 0.000 description 1
- 229940064734 aminobenzoate Drugs 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- YFNONBGXNFCTMM-UHFFFAOYSA-N butoxybenzene Chemical compound CCCCOC1=CC=CC=C1 YFNONBGXNFCTMM-UHFFFAOYSA-N 0.000 description 1
- VHRGRCVQAFMJIZ-UHFFFAOYSA-N cadaverine Chemical compound NCCCCCN VHRGRCVQAFMJIZ-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 239000012295 chemical reaction liquid Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000007810 chemical reaction solvent Substances 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000006103 coloring component Substances 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- VKIRRGRTJUUZHS-UHFFFAOYSA-N cyclohexane-1,4-diamine Chemical compound NC1CCC(N)CC1 VKIRRGRTJUUZHS-UHFFFAOYSA-N 0.000 description 1
- 239000012024 dehydrating agents Substances 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 150000001987 diarylethers Chemical class 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000004210 ether based solvent Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
- 239000012433 hydrogen halide Substances 0.000 description 1
- 229910000039 hydrogen halide Inorganic materials 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 239000003350 kerosene Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- XIXADJRWDQXREU-UHFFFAOYSA-M lithium acetate Chemical compound [Li+].CC([O-])=O XIXADJRWDQXREU-UHFFFAOYSA-M 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- CQDGTJPVBWZJAZ-UHFFFAOYSA-N monoethyl carbonate Chemical compound CCOC(O)=O CQDGTJPVBWZJAZ-UHFFFAOYSA-N 0.000 description 1
- AJFDBNQQDYLMJN-UHFFFAOYSA-N n,n-diethylacetamide Chemical compound CCN(CC)C(C)=O AJFDBNQQDYLMJN-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920001521 polyalkylene glycol ether Chemical class 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 238000007867 post-reaction treatment Methods 0.000 description 1
- 235000011056 potassium acetate Nutrition 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- WYVAMUWZEOHJOQ-UHFFFAOYSA-N propionic anhydride Chemical compound CCC(=O)OC(=O)CC WYVAMUWZEOHJOQ-UHFFFAOYSA-N 0.000 description 1
- FOWDZVNRQHPXDO-UHFFFAOYSA-N propyl hydrogen carbonate Chemical compound CCCOC(O)=O FOWDZVNRQHPXDO-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000011403 purification operation Methods 0.000 description 1
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000036632 reaction speed Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000013517 stratification Methods 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000004154 testing of material Methods 0.000 description 1
- 238000001269 time-of-flight mass spectrometry Methods 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- YFNKIDBQEZZDLK-UHFFFAOYSA-N triglyme Chemical compound COCCOCCOCCOC YFNKIDBQEZZDLK-UHFFFAOYSA-N 0.000 description 1
- 239000010887 waste solvent Substances 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 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
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
- C08G73/16—Polyester-imides
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Compositions Of Macromolecular Compounds (AREA)
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2019-150805 | 2019-08-21 | ||
| JP2019150805 | 2019-08-21 |
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|---|---|
| TW202115157A TW202115157A (zh) | 2021-04-16 |
| TWI853070B true TWI853070B (zh) | 2024-08-21 |
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| JP (2) | JPWO2021033655A1 (enrdf_load_stackoverflow) |
| KR (1) | KR20220051330A (enrdf_load_stackoverflow) |
| CN (1) | CN114222778B (enrdf_load_stackoverflow) |
| TW (1) | TWI853070B (enrdf_load_stackoverflow) |
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Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200948862A (en) * | 2008-05-16 | 2009-12-01 | Asahi Chemical Ind | Polyester-imide precursor and polyester-imide |
| CN104640907A (zh) * | 2012-09-19 | 2015-05-20 | 本州化学工业株式会社 | 聚酰亚胺及其成形体 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58219238A (ja) * | 1982-06-15 | 1983-12-20 | Mitsui Toatsu Chem Inc | 芳香族ポリアミド−ポリイミド共重合体の製造法 |
| JPS62227953A (ja) * | 1986-03-28 | 1987-10-06 | Hitachi Chem Co Ltd | ポリイミド樹脂組成物 |
| JPH0660249B2 (ja) * | 1988-08-18 | 1994-08-10 | イー・アイ・デユポン・デ・ニモアス・アンド・カンパニー | 溶媒抽出によるポリイミド分子量の向上 |
| JP5037759B2 (ja) * | 2001-04-25 | 2012-10-03 | 株式会社カネカ | ポリイミドフィルムおよびそのポリイミドフィルムを用いたフレキシブルプリント基板 |
| JP2003238684A (ja) * | 2002-02-15 | 2003-08-27 | New Japan Chem Co Ltd | ポリアミド酸溶液の製造方法 |
| JP2008101187A (ja) * | 2006-09-19 | 2008-05-01 | Asahi Kasei Corp | ポリエステルイミドおよびその製造方法 |
| US9023974B2 (en) * | 2007-01-26 | 2015-05-05 | Honshu Chemical Industry Co., Ltd. | Ester group-containing tetracarboxylic acid dianhydride, novel polyesterimide precursor derived therefrom, and polyesterimide |
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- 2020-08-17 JP JP2021540933A patent/JPWO2021033655A1/ja active Pending
- 2020-08-17 WO PCT/JP2020/030935 patent/WO2021033655A1/ja active Application Filing
- 2020-08-17 CN CN202080054438.1A patent/CN114222778B/zh active Active
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200948862A (en) * | 2008-05-16 | 2009-12-01 | Asahi Chemical Ind | Polyester-imide precursor and polyester-imide |
| CN104640907A (zh) * | 2012-09-19 | 2015-05-20 | 本州化学工业株式会社 | 聚酰亚胺及其成形体 |
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| TW202115157A (zh) | 2021-04-16 |
| JPWO2021033655A1 (enrdf_load_stackoverflow) | 2021-02-25 |
| JP2025032249A (ja) | 2025-03-11 |
| CN114222778A (zh) | 2022-03-22 |
| KR20220051330A (ko) | 2022-04-26 |
| CN114222778B (zh) | 2023-11-14 |
| WO2021033655A1 (ja) | 2021-02-25 |
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