JP2022526988A - 柔軟な光硬化性シアノアクリレート組成物 - Google Patents
柔軟な光硬化性シアノアクリレート組成物 Download PDFInfo
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- JP2022526988A JP2022526988A JP2021559269A JP2021559269A JP2022526988A JP 2022526988 A JP2022526988 A JP 2022526988A JP 2021559269 A JP2021559269 A JP 2021559269A JP 2021559269 A JP2021559269 A JP 2021559269A JP 2022526988 A JP2022526988 A JP 2022526988A
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- 239000000203 mixture Substances 0.000 title claims abstract description 84
- 229920001651 Cyanoacrylate Polymers 0.000 title claims abstract description 45
- MWCLLHOVUTZFKS-UHFFFAOYSA-N Methyl cyanoacrylate Chemical compound COC(=O)C(=C)C#N MWCLLHOVUTZFKS-UHFFFAOYSA-N 0.000 title claims abstract description 31
- 239000004014 plasticizer Substances 0.000 claims abstract description 33
- 239000007795 chemical reaction product Substances 0.000 claims abstract description 16
- 239000000758 substrate Substances 0.000 claims description 18
- -1 alkylene compound Chemical class 0.000 claims description 15
- 239000000853 adhesive Substances 0.000 claims description 13
- 230000001070 adhesive effect Effects 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 229920000515 polycarbonate Polymers 0.000 claims description 8
- 239000004417 polycarbonate Substances 0.000 claims description 8
- 239000003381 stabilizer Substances 0.000 claims description 8
- 238000012360 testing method Methods 0.000 claims description 6
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- 125000005907 alkyl ester group Chemical group 0.000 claims description 5
- VTJUKNSKBAOEHE-UHFFFAOYSA-N calixarene Chemical compound 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 5
- 229920001223 polyethylene glycol Polymers 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 4
- 150000003983 crown ethers Chemical class 0.000 claims description 3
- 150000002440 hydroxy compounds Chemical class 0.000 claims description 3
- 239000002562 thickening agent Substances 0.000 claims description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 2
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- 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 claims description 2
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- VFHVQBAGLAREND-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 VFHVQBAGLAREND-UHFFFAOYSA-N 0.000 description 4
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- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- KTZLFESZLNIZGM-UHFFFAOYSA-N 5-butoxy-2-cyanopent-2-enoic acid Chemical compound CCCCOCCC=C(C#N)C(O)=O KTZLFESZLNIZGM-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
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- 239000004830 Super Glue Substances 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
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- 238000011156 evaluation Methods 0.000 description 2
- 229910052735 hafnium Inorganic materials 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
- 229910052748 manganese Inorganic materials 0.000 description 2
- 239000011572 manganese Substances 0.000 description 2
- 150000004702 methyl esters Chemical class 0.000 description 2
- 229910052750 molybdenum Inorganic materials 0.000 description 2
- 229910052758 niobium Inorganic materials 0.000 description 2
- RPQUGMLCZLGZTG-UHFFFAOYSA-N octyl cyanoacrylate Chemical compound CCCCCCCCOC(=O)C(=C)C#N RPQUGMLCZLGZTG-UHFFFAOYSA-N 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- ITCZEZQMUWEPQP-UHFFFAOYSA-N prop-2-enyl 2-cyanoprop-2-enoate Chemical compound C=CCOC(=O)C(=C)C#N ITCZEZQMUWEPQP-UHFFFAOYSA-N 0.000 description 2
- 229910052721 tungsten Inorganic materials 0.000 description 2
- 229910052720 vanadium Inorganic materials 0.000 description 2
- 229910052724 xenon Inorganic materials 0.000 description 2
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 2
- 229910052727 yttrium Inorganic materials 0.000 description 2
- 229910052726 zirconium Inorganic materials 0.000 description 2
- VEJOYRPGKZZTJW-FDGPNNRMSA-N (z)-4-hydroxypent-3-en-2-one;platinum Chemical compound [Pt].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O VEJOYRPGKZZTJW-FDGPNNRMSA-N 0.000 description 1
- KZPYGQFFRCFCPP-UHFFFAOYSA-N 1,1'-bis(diphenylphosphino)ferrocene Chemical compound [Fe+2].C1=CC=C[C-]1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=C[C-]1P(C=1C=CC=CC=1)C1=CC=CC=C1 KZPYGQFFRCFCPP-UHFFFAOYSA-N 0.000 description 1
- WFUDBPZFGCNRDM-UHFFFAOYSA-N 1-butylcyclopenta-1,3-diene;cyclopenta-1,3-diene;iron(2+) Chemical compound [Fe+2].C=1C=C[CH-]C=1.CCCCC1=CC=C[CH-]1 WFUDBPZFGCNRDM-UHFFFAOYSA-N 0.000 description 1
- VFTFKUDGYRBSAL-UHFFFAOYSA-N 15-crown-5 Chemical compound C1COCCOCCOCCOCCO1 VFTFKUDGYRBSAL-UHFFFAOYSA-N 0.000 description 1
- XEZNGIUYQVAUSS-UHFFFAOYSA-N 18-crown-6 Chemical compound C1COCCOCCOCCOCCOCCO1 XEZNGIUYQVAUSS-UHFFFAOYSA-N 0.000 description 1
- AXWCVSOBRFLCJG-UHFFFAOYSA-N 2,5,12,15,22,25-hexaoxatetracyclo[24.4.0.06,11.016,21]triaconta-1(30),6,8,10,16,18,20,26,28-nonaene Chemical compound O1CCOC2=CC=CC=C2OCCOC2=CC=CC=C2OCCOC2=CC=CC=C21 AXWCVSOBRFLCJG-UHFFFAOYSA-N 0.000 description 1
- YPUCMXNIBKZZOC-UHFFFAOYSA-N 2-(cyanomethylidene)hex-3-enoic acid Chemical compound CCC=CC(=CC#N)C(=O)O YPUCMXNIBKZZOC-UHFFFAOYSA-N 0.000 description 1
- UHFFVFAKEGKNAQ-UHFFFAOYSA-N 2-benzyl-2-(dimethylamino)-1-(4-morpholin-4-ylphenyl)butan-1-one Chemical compound C=1C=C(N2CCOCC2)C=CC=1C(=O)C(CC)(N(C)C)CC1=CC=CC=C1 UHFFVFAKEGKNAQ-UHFFFAOYSA-N 0.000 description 1
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- FCEOGYWNOSBEPV-FDGPNNRMSA-N cobalt;(z)-4-hydroxypent-3-en-2-one Chemical compound [Co].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O FCEOGYWNOSBEPV-FDGPNNRMSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
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- ZKXWKVVCCTZOLD-FDGPNNRMSA-N copper;(z)-4-hydroxypent-3-en-2-one Chemical compound [Cu].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O ZKXWKVVCCTZOLD-FDGPNNRMSA-N 0.000 description 1
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- KOMDZQSPRDYARS-UHFFFAOYSA-N cyclopenta-1,3-diene titanium Chemical compound [Ti].C1C=CC=C1.C1C=CC=C1 KOMDZQSPRDYARS-UHFFFAOYSA-N 0.000 description 1
- VGBAECKRTWHKHC-UHFFFAOYSA-N cyclopenta-1,3-diene;1-ethenylcyclopenta-1,3-diene;iron(2+) Chemical compound [Fe+2].C=1C=C[CH-]C=1.[CH2-]C=C1C=CC=C1 VGBAECKRTWHKHC-UHFFFAOYSA-N 0.000 description 1
- YSSSPARMOAYJTE-UHFFFAOYSA-N dibenzo-18-crown-6 Chemical compound O1CCOCCOC2=CC=CC=C2OCCOCCOC2=CC=CC=C21 YSSSPARMOAYJTE-UHFFFAOYSA-N 0.000 description 1
- MXCSCGGRLMRZMF-UHFFFAOYSA-N dibenzo-30-crown-10 Chemical compound O1CCOCCOCCOCCOC2=CC=CC=C2OCCOCCOCCOCCOC2=CC=CC=C21 MXCSCGGRLMRZMF-UHFFFAOYSA-N 0.000 description 1
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- QMLGNDFKJAFKGZ-UHFFFAOYSA-N dicyclohexano-24-crown-8 Chemical compound O1CCOCCOCCOC2CCCCC2OCCOCCOCCOC2CCCCC21 QMLGNDFKJAFKGZ-UHFFFAOYSA-N 0.000 description 1
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- 229940117360 ethyl pyruvate Drugs 0.000 description 1
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- FNVQIYPKWVVQID-UHFFFAOYSA-N oxolan-2-ylmethyl 2-cyanoprop-2-enoate Chemical compound N#CC(=C)C(=O)OCC1CCCO1 FNVQIYPKWVVQID-UHFFFAOYSA-N 0.000 description 1
- AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 1
- JLFNLZLINWHATN-UHFFFAOYSA-N pentaethylene glycol Chemical compound OCCOCCOCCOCCOCCO JLFNLZLINWHATN-UHFFFAOYSA-N 0.000 description 1
- 238000000016 photochemical curing Methods 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
- ZTYMNUBYYQNBFP-UHFFFAOYSA-N propyl 2-cyanoprop-2-enoate Chemical compound CCCOC(=O)C(=C)C#N ZTYMNUBYYQNBFP-UHFFFAOYSA-N 0.000 description 1
- ILPVOWZUBFRIAX-UHFFFAOYSA-N propyl 2-oxopropanoate Chemical compound CCCOC(=O)C(C)=O ILPVOWZUBFRIAX-UHFFFAOYSA-N 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000010944 silver (metal) Substances 0.000 description 1
- 125000005415 substituted alkoxy group Chemical group 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- VPYJNCGUESNPMV-UHFFFAOYSA-N triallylamine Chemical compound C=CCN(CC=C)CC=C VPYJNCGUESNPMV-UHFFFAOYSA-N 0.000 description 1
- RJIFVNWOLLIBJV-UHFFFAOYSA-N tributyl benzene-1,2,4-tricarboxylate Chemical compound CCCCOC(=O)C1=CC=C(C(=O)OCCCC)C(C(=O)OCCCC)=C1 RJIFVNWOLLIBJV-UHFFFAOYSA-N 0.000 description 1
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- ODHXBMXNKOYIBV-UHFFFAOYSA-N triphenylamine Chemical compound C1=CC=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 ODHXBMXNKOYIBV-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
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Abstract
Description
様々なメタロセンが本明細書で使用するのに適している。本明細書において特に関心のある材料は、構造I内のメタロセンによって表されてよい。
A及びA’は同一でも異なってもよく、C又はNであってよく;
m及びm’は同一でも異なってもよく、1又は2であってよく;
MeはFe、Ti、Ru、Co、Ni、Cr、Cu、Mn、Pd、Ag、Rh、Pt、Zr、Hf、Nb、V、Mo等である。)
本発明組成物に有用なシラクラウン化合物の具体例は、次のとおりである。
本発明は、以下の実施例によってさらに説明される。
以下の表4は、様々な評価の観察結果を示している。
Claims (24)
- (a)シアノアクリレート成分、(b)メタロセン成分、(c)光開始剤成分、及び(d)可塑剤成分を含むシアノアクリレート組成物。
- 前記可塑剤成分が、複数のアルキルエステル置換基及び/又はその逆アルキルエステル置換基を有する短鎖アルキレン化合物である、請求項1に記載の組成物。
- 前記可塑剤成分が、鎖中に3個又は4個の炭素原子を有する短鎖アルキレン化合物である、請求項1に記載の組成物。
- 前記可塑剤成分が、直鎖を有する短鎖アルキレン化合物である、請求項1に記載の組成物。
- 前記可塑剤成分が、2~4の置換基を有する短鎖アルキレン化合物である、請求項1に記載の組成物。
- 前記可塑剤成分が、複数のアルキルエステル置換基及び/又はその逆アルキルエステル置換基を有する短鎖アルキレン化合物であり、前記アルキルエステル及び/又は逆アルキルエステルが、C1‐3アルキルエステル及び/又は逆アルキルエステルを有する、請求項1に記載の組成物。
- 前記可塑剤成分が約10重量%~約30重量%の量で存在する、請求項1に記載の組成物。
- 前記可塑剤成分が約15重量%~約35重量%の量で存在する、請求項1に記載の組成物。
- 前記可塑剤成分が約15重量%~約20重量%の量で存在する、請求項1に記載の組成物。
- 安定剤をさらに含む、請求項1に記載の組成物。
- 安定量の酸性安定剤、及びフリーラジカル阻害剤をさらに含む、請求項1に記載の組成物。
- 促進剤成分をさらに含む、請求項1に記載の組成物。
- 前記促進剤成分が、カリックスアレーン、オキサカリックスアレーン、シラクラウン、シクロデキストリン、クラウンエーテル、ポリ(エチレングリコール)ジ(メタ)アクリレート、エトキシル化ヒドロキシ化合物、及びそれらの組み合わせから成る群から選択される、請求項13に記載の組成物。
- 強化剤、耐衝撃性添加剤、チキソトロピー付与剤、増粘剤、染料、及びそれらの組み合わせから成る群から選択される添加剤をさらに含む、請求項1に記載の組成物。
- 請求項1に記載の組成物の反応生成物。
- 前記反応生成物が、実質的に相分離を示さない、請求項1に記載の組成物。
- 前記反応生成物が、約35%超過の破断点伸びを示す、請求項1に記載の組成物。
- 前記反応生成物が、約125%超過の破断点伸びを示す、請求項1に記載の組成物。
- 前記反応生成物が、約1800psi超過のポリカーボネート上でのブロックせん断強度を示す、請求項1に記載の組成物。
- 前記反応生成物が、約1900psi超過のポリカーボネート上でのブロックせん断強度を示す、請求項1に記載の組成物。
- 前記反応生成物が、約2200psi超過のポリカーボネート上でのブロックせん断強度を示す、請求項1に記載の組成物。
- 前記反応生成物が、スイング試験で約60サイクル超過を示す、請求項1に記載の組成物。
- そのうちの少なくとも1つが熱可塑性材料で構成されている2つの基材を結合する方法であって:
請求項1に記載のシアノアクリレート組成物を、少なくとも1つの基材に塗布する工程、及び
接着剤が固定するのに十分な時間、前記基材を接合する工程、
を含む、方法。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US201962829273P | 2019-04-04 | 2019-04-04 | |
US62/829,273 | 2019-04-04 | ||
PCT/US2020/026789 WO2020206405A1 (en) | 2019-04-04 | 2020-04-05 | Flexible photocurable cyanoacrylate compositions |
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JP2022526988A true JP2022526988A (ja) | 2022-05-27 |
Family
ID=72666297
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JP2021559269A Pending JP2022526988A (ja) | 2019-04-04 | 2020-04-05 | 柔軟な光硬化性シアノアクリレート組成物 |
Country Status (6)
Country | Link |
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US (1) | US20220033544A1 (ja) |
EP (1) | EP3947586A4 (ja) |
JP (1) | JP2022526988A (ja) |
KR (1) | KR20210136134A (ja) |
CN (1) | CN113874459B (ja) |
WO (1) | WO2020206405A1 (ja) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2022187848A1 (en) | 2021-03-05 | 2022-09-09 | H.B. Fuller Company | Cyanoacrylate composition with hazardless stabilizer |
CN114561154B (zh) * | 2022-02-28 | 2022-10-28 | 浙江久而久化学有限公司 | 一种uv、湿气双固瞬干胶及其制备方法 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
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TW369554B (en) * | 1995-10-19 | 1999-09-11 | Three Bond Co Ltd | Photocurable composition |
US5922783A (en) * | 1997-02-27 | 1999-07-13 | Loctite Corporation | Radiation-curable, cyanoacrylate-containing compositions |
DE60129603T2 (de) * | 2001-01-08 | 2008-05-21 | Loctite (R & D) Ltd., Tallaght | Zu flexiblen polymermaterialien aushärtbare cyanoacrylatmassen |
US20100213096A1 (en) * | 2007-06-12 | 2010-08-26 | Clast Trading Limited | Cyanoacrylate Adhesive Compositions and Devices and Process for Sterilization Thereof |
JP5434771B2 (ja) * | 2010-04-27 | 2014-03-05 | 東亞合成株式会社 | 接着方法 |
EP3124509A1 (en) * | 2015-07-31 | 2017-02-01 | Afinitica Technologies, S. L. | Fast light curing cyanoacrylate compositions |
-
2020
- 2020-04-05 EP EP20784275.8A patent/EP3947586A4/en active Pending
- 2020-04-05 KR KR1020217034278A patent/KR20210136134A/ko unknown
- 2020-04-05 JP JP2021559269A patent/JP2022526988A/ja active Pending
- 2020-04-05 CN CN202080039839.XA patent/CN113874459B/zh active Active
- 2020-04-05 WO PCT/US2020/026789 patent/WO2020206405A1/en unknown
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2021
- 2021-10-04 US US17/493,641 patent/US20220033544A1/en active Pending
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US20220033544A1 (en) | 2022-02-03 |
KR20210136134A (ko) | 2021-11-16 |
CN113874459A (zh) | 2021-12-31 |
EP3947586A1 (en) | 2022-02-09 |
WO2020206405A1 (en) | 2020-10-08 |
EP3947586A4 (en) | 2023-01-04 |
CN113874459B (zh) | 2023-07-04 |
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