KR20230164004A - 경화성 접착제 조성물, 및 경화물 - Google Patents
경화성 접착제 조성물, 및 경화물 Download PDFInfo
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- KR20230164004A KR20230164004A KR1020237026434A KR20237026434A KR20230164004A KR 20230164004 A KR20230164004 A KR 20230164004A KR 1020237026434 A KR1020237026434 A KR 1020237026434A KR 20237026434 A KR20237026434 A KR 20237026434A KR 20230164004 A KR20230164004 A KR 20230164004A
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- adhesive composition
- curable adhesive
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- component
- cured product
- Prior art date
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- 239000000853 adhesive Substances 0.000 title claims abstract description 226
- 230000001070 adhesive effect Effects 0.000 title claims abstract description 226
- 239000000203 mixture Substances 0.000 title claims abstract description 186
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- 239000011347 resin Substances 0.000 claims abstract description 126
- 239000003431 cross linking reagent Substances 0.000 claims abstract description 76
- 239000011230 binding agent Substances 0.000 claims abstract description 45
- 125000000524 functional group Chemical group 0.000 claims abstract description 29
- 239000004480 active ingredient Substances 0.000 claims abstract description 21
- 150000001875 compounds Chemical class 0.000 claims description 109
- 229920001955 polyphenylene ether Polymers 0.000 claims description 45
- 238000000034 method Methods 0.000 claims description 39
- 238000010538 cationic polymerization reaction Methods 0.000 claims description 21
- 239000003505 polymerization initiator Substances 0.000 claims description 20
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- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical group OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims description 16
- 229920001187 thermosetting polymer Polymers 0.000 claims description 13
- 239000007788 liquid Substances 0.000 claims description 9
- 239000012787 coverlay film Substances 0.000 claims description 7
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 7
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 238000001723 curing Methods 0.000 description 71
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- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 150000001491 aromatic compounds Chemical class 0.000 description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
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- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 238000003475 lamination Methods 0.000 description 3
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
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- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 description 2
- HASUCEDGKYJBDC-UHFFFAOYSA-N 1-[3-[[bis(oxiran-2-ylmethyl)amino]methyl]cyclohexyl]-n,n-bis(oxiran-2-ylmethyl)methanamine Chemical compound C1OC1CN(CC1CC(CN(CC2OC2)CC2OC2)CCC1)CC1CO1 HASUCEDGKYJBDC-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 239000004642 Polyimide Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 150000008065 acid anhydrides Chemical group 0.000 description 2
- 229940091181 aconitic acid Drugs 0.000 description 2
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 125000005370 alkoxysilyl group Chemical group 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
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- 125000002091 cationic group Chemical group 0.000 description 2
- GTZCVFVGUGFEME-IWQZZHSRSA-N cis-aconitic acid Chemical compound OC(=O)C\C(C(O)=O)=C\C(O)=O GTZCVFVGUGFEME-IWQZZHSRSA-N 0.000 description 2
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- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
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- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical class I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 2
- SHFJWMWCIHQNCP-UHFFFAOYSA-M hydron;tetrabutylazanium;sulfate Chemical compound OS([O-])(=O)=O.CCCC[N+](CCCC)(CCCC)CCCC SHFJWMWCIHQNCP-UHFFFAOYSA-M 0.000 description 2
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- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229910021645 metal ion Inorganic materials 0.000 description 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 2
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- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
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- 125000003396 thiol group Chemical group [H]S* 0.000 description 2
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 2
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- SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 1
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- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
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- C09J7/00—Adhesives in the form of films or foils
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
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- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K3/00—Apparatus or processes for manufacturing printed circuits
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| PCT/JP2022/015341 WO2022210671A1 (ja) | 2021-03-30 | 2022-03-29 | 硬化性接着剤組成物、及び硬化物 |
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| JP6172520B2 (ja) * | 2013-10-31 | 2017-08-02 | パナソニックIpマネジメント株式会社 | 樹脂組成物、プリプレグ、金属張積層板、及びプリント配線板 |
| JP6335384B2 (ja) * | 2015-03-13 | 2018-05-30 | 京セラ株式会社 | 樹脂組成物、プリプレグ、金属張積層板および配線基板 |
| JP6074698B1 (ja) * | 2015-07-31 | 2017-02-08 | 東洋インキScホールディングス株式会社 | 熱硬化性接着シート、およびその利用 |
| JP2018035226A (ja) * | 2016-08-30 | 2018-03-08 | リンテック株式会社 | 粘着剤組成物、及び粘着シート |
| JP6921586B2 (ja) * | 2017-03-31 | 2021-08-18 | リンテック株式会社 | 粘着性組成物、粘着剤、粘着シートおよび表示体 |
| JP7375364B2 (ja) * | 2018-08-21 | 2023-11-08 | 東洋紡エムシー株式会社 | 接着剤組成物、積層体、およびリチウムイオン電池用包装材料 |
| CN114207068B (zh) * | 2019-09-06 | 2024-04-02 | 东洋纺Mc株式会社 | 聚烯烃系粘接剂组合物 |
| JP2021161130A (ja) * | 2020-03-30 | 2021-10-11 | 東洋紡株式会社 | ダイマージオール共重合ポリイミドウレタン樹脂及び前記樹脂を含む接着剤組成物 |
| JP7173252B2 (ja) * | 2020-09-24 | 2022-11-16 | 三菱ケミカル株式会社 | 粘着剤組成物、粘着剤及び粘着剤層 |
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| CN117098825A8 (zh) | 2023-12-22 |
| JPWO2022210671A1 (https=) | 2022-10-06 |
| WO2022210671A1 (ja) | 2022-10-06 |
| TW202248387A (zh) | 2022-12-16 |
| CN117098825A (zh) | 2023-11-21 |
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