JP6461924B2 - シアノアクリレート組成物 - Google Patents
シアノアクリレート組成物 Download PDFInfo
- Publication number
- JP6461924B2 JP6461924B2 JP2016515020A JP2016515020A JP6461924B2 JP 6461924 B2 JP6461924 B2 JP 6461924B2 JP 2016515020 A JP2016515020 A JP 2016515020A JP 2016515020 A JP2016515020 A JP 2016515020A JP 6461924 B2 JP6461924 B2 JP 6461924B2
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- JP
- Japan
- Prior art keywords
- crown
- cyanoacrylate
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- weight percent
- amount
- 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.)
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- 239000000203 mixture Substances 0.000 title claims description 61
- 229920001651 Cyanoacrylate Polymers 0.000 title claims description 55
- MWCLLHOVUTZFKS-UHFFFAOYSA-N Methyl cyanoacrylate Chemical compound COC(=O)C(=C)C#N MWCLLHOVUTZFKS-UHFFFAOYSA-N 0.000 title claims description 51
- 239000000758 substrate Substances 0.000 claims description 19
- RPQUGMLCZLGZTG-UHFFFAOYSA-N octyl cyanoacrylate Chemical compound CCCCCCCCOC(=O)C(=C)C#N RPQUGMLCZLGZTG-UHFFFAOYSA-N 0.000 claims description 12
- 239000000853 adhesive Substances 0.000 claims description 9
- 230000001070 adhesive effect Effects 0.000 claims description 9
- FGBJXOREULPLGL-UHFFFAOYSA-N ethyl cyanoacrylate Chemical compound CCOC(=O)C(=C)C#N FGBJXOREULPLGL-UHFFFAOYSA-N 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- WEAPVABOECTMGR-UHFFFAOYSA-N triethyl 2-acetyloxypropane-1,2,3-tricarboxylate Chemical compound CCOC(=O)CC(C(=O)OCC)(OC(C)=O)CC(=O)OCC WEAPVABOECTMGR-UHFFFAOYSA-N 0.000 claims description 8
- 229920000858 Cyclodextrin Polymers 0.000 claims description 5
- 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 5
- 239000003381 stabilizer Substances 0.000 claims description 5
- 150000003983 crown ethers Chemical class 0.000 claims description 4
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 3
- 239000000654 additive Substances 0.000 claims description 3
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- 150000002440 hydroxy compounds Chemical class 0.000 claims description 3
- 229920001223 polyethylene glycol Polymers 0.000 claims description 3
- 239000000047 product Substances 0.000 claims description 3
- XEZNGIUYQVAUSS-UHFFFAOYSA-N 18-crown-6 Chemical compound C1COCCOCCOCCOCCOCCO1 XEZNGIUYQVAUSS-UHFFFAOYSA-N 0.000 claims description 2
- 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 claims description 2
- SVJYFWHFQPBIOY-UHFFFAOYSA-N 7,8,16,17-tetrahydro-6h,15h-dibenzo[b,i][1,4,8,11]tetraoxacyclotetradecine Chemical compound O1CCCOC2=CC=CC=C2OCCCOC2=CC=CC=C21 SVJYFWHFQPBIOY-UHFFFAOYSA-N 0.000 claims description 2
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- YSSSPARMOAYJTE-UHFFFAOYSA-N dibenzo-18-crown-6 Chemical compound O1CCOCCOC2=CC=CC=C2OCCOCCOC2=CC=CC=C21 YSSSPARMOAYJTE-UHFFFAOYSA-N 0.000 claims description 2
- MXCSCGGRLMRZMF-UHFFFAOYSA-N dibenzo-30-crown-10 Chemical compound O1CCOCCOCCOCCOC2=CC=CC=C2OCCOCCOCCOCCOC2=CC=CC=C21 MXCSCGGRLMRZMF-UHFFFAOYSA-N 0.000 claims description 2
- BBGKDYHZQOSNMU-UHFFFAOYSA-N dicyclohexano-18-crown-6 Chemical compound O1CCOCCOC2CCCCC2OCCOCCOC2CCCCC21 BBGKDYHZQOSNMU-UHFFFAOYSA-N 0.000 claims description 2
- QMLGNDFKJAFKGZ-UHFFFAOYSA-N dicyclohexano-24-crown-8 Chemical compound O1CCOCCOCCOC2CCCCC2OCCOCCOCCOC2CCCCC21 QMLGNDFKJAFKGZ-UHFFFAOYSA-N 0.000 claims description 2
- 150000003254 radicals Chemical class 0.000 claims description 2
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- 230000000996 additive effect Effects 0.000 claims 2
- 239000012815 thermoplastic material Substances 0.000 claims 2
- 150000003985 15-crown-5 derivatives Chemical group 0.000 claims 1
- DOOTYTYQINUNNV-UHFFFAOYSA-N Triethyl citrate Chemical compound CCOC(=O)CC(O)(C(=O)OCC)CC(=O)OCC DOOTYTYQINUNNV-UHFFFAOYSA-N 0.000 claims 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 claims 1
- 230000000087 stabilizing effect Effects 0.000 claims 1
- 239000012745 toughening agent Substances 0.000 claims 1
- 239000001069 triethyl citrate Substances 0.000 claims 1
- VMYFZRTXGLUXMZ-UHFFFAOYSA-N triethyl citrate Natural products CCOC(=O)C(O)(C(=O)OCC)C(=O)OCC VMYFZRTXGLUXMZ-UHFFFAOYSA-N 0.000 claims 1
- 235000013769 triethyl citrate Nutrition 0.000 claims 1
- 230000035882 stress Effects 0.000 description 11
- 239000004014 plasticizer Substances 0.000 description 10
- 239000004800 polyvinyl chloride Substances 0.000 description 10
- 229920000915 polyvinyl chloride Polymers 0.000 description 10
- 239000000178 monomer Substances 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 229920003023 plastic Polymers 0.000 description 6
- 239000004033 plastic Substances 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 5
- 230000000712 assembly Effects 0.000 description 5
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- 239000002861 polymer material Substances 0.000 description 5
- 239000004830 Super Glue Substances 0.000 description 4
- 229940053009 ethyl cyanoacrylate Drugs 0.000 description 4
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- WNMUOLOGFSYABW-UHFFFAOYSA-N 2-butoxyethyl 2-cyanoprop-2-enoate Chemical compound CCCCOCCOC(=O)C(=C)C#N WNMUOLOGFSYABW-UHFFFAOYSA-N 0.000 description 2
- XXISUJVWOBVITO-UHFFFAOYSA-N 2-propoxyethyl 2-cyanoprop-2-enoate Chemical compound CCCOCCOC(=O)C(=C)C#N XXISUJVWOBVITO-UHFFFAOYSA-N 0.000 description 2
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 2
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
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- 238000005259 measurement Methods 0.000 description 2
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- 238000009864 tensile test Methods 0.000 description 2
- VFTFKUDGYRBSAL-UHFFFAOYSA-N 15-crown-5 Chemical compound C1COCCOCCOCCOCCO1 VFTFKUDGYRBSAL-UHFFFAOYSA-N 0.000 description 1
- VYPNMUSYTNBGQH-UHFFFAOYSA-N 2,2-dimethyl-1,3,6,9,12,15-hexaoxa-2-silacycloheptadecane Chemical compound C[Si]1(C)OCCOCCOCCOCCOCCO1 VYPNMUSYTNBGQH-UHFFFAOYSA-N 0.000 description 1
- YNLJHXFENQDVSS-UHFFFAOYSA-N 2,2-dimethylpropyl 2-cyanoprop-2-enoate Chemical compound CC(C)(C)COC(=O)C(=C)C#N YNLJHXFENQDVSS-UHFFFAOYSA-N 0.000 description 1
- IOARUBDCMGYRAT-UHFFFAOYSA-N 2-butoxypropan-2-yl 2-cyanoprop-2-enoate Chemical compound CCCCOC(C)(C)OC(=O)C(=C)C#N IOARUBDCMGYRAT-UHFFFAOYSA-N 0.000 description 1
- SYHYPVSEIMDSAC-UHFFFAOYSA-N 2-cyano-4-methylhex-2-enoic acid Chemical compound CCC(C)C=C(C#N)C(O)=O SYHYPVSEIMDSAC-UHFFFAOYSA-N 0.000 description 1
- LUNMJRJMSXZSLC-UHFFFAOYSA-N 2-cyclopropylethanol Chemical compound OCCC1CC1 LUNMJRJMSXZSLC-UHFFFAOYSA-N 0.000 description 1
- IQDPHMACOQAPBQ-UHFFFAOYSA-N 2-ethoxyethyl 2-cyanoprop-2-enoate Chemical compound CCOCCOC(=O)C(=C)C#N IQDPHMACOQAPBQ-UHFFFAOYSA-N 0.000 description 1
- HMLDHWZWDUUHHJ-UHFFFAOYSA-N 2-ethoxypropan-2-yl 2-cyanoprop-2-enoate Chemical compound CCOC(C)(C)OC(=O)C(=C)C#N HMLDHWZWDUUHHJ-UHFFFAOYSA-N 0.000 description 1
- RYUQUOCOVTVPOA-UHFFFAOYSA-N 2-methoxypropan-2-yl 2-cyanoprop-2-enoate Chemical compound COC(C)(C)OC(=O)C(=C)C#N RYUQUOCOVTVPOA-UHFFFAOYSA-N 0.000 description 1
- LTYWEEUBKYARKZ-UHFFFAOYSA-N 2-phenylethyl 2-cyanoprop-2-enoate Chemical compound N#CC(=C)C(=O)OCCC1=CC=CC=C1 LTYWEEUBKYARKZ-UHFFFAOYSA-N 0.000 description 1
- SJONHNRVTBLSRU-UHFFFAOYSA-N 3-butoxypropyl 2-cyanoprop-2-enoate Chemical compound CCCCOCCCOC(=O)C(=C)C#N SJONHNRVTBLSRU-UHFFFAOYSA-N 0.000 description 1
- LOZOGMFSIMWOPP-UHFFFAOYSA-N 3-chloropropyl 2-cyanoprop-2-enoate Chemical compound ClCCCOC(=O)C(=C)C#N LOZOGMFSIMWOPP-UHFFFAOYSA-N 0.000 description 1
- IGKQGKYWAQQHGB-UHFFFAOYSA-N 3-ethoxypropyl 2-cyanoprop-2-enoate Chemical compound CCOCCCOC(=O)C(=C)C#N IGKQGKYWAQQHGB-UHFFFAOYSA-N 0.000 description 1
- PFSVSOOFNDBGMO-UHFFFAOYSA-N 3-methoxypropyl 2-cyanoprop-2-enoate Chemical compound COCCCOC(=O)C(=C)C#N PFSVSOOFNDBGMO-UHFFFAOYSA-N 0.000 description 1
- UPLMBGKAEBVNAU-UHFFFAOYSA-N 3-propoxypropyl 2-cyanoprop-2-enoate Chemical compound CCCOCCCOC(=O)C(=C)C#N UPLMBGKAEBVNAU-UHFFFAOYSA-N 0.000 description 1
- RLFFAWYYTKPTCZ-UHFFFAOYSA-N 4-butoxybutyl 2-cyanoprop-2-enoate Chemical compound CCCCOCCCCOC(=O)C(=C)C#N RLFFAWYYTKPTCZ-UHFFFAOYSA-N 0.000 description 1
- BZWFBZZBLILDAC-UHFFFAOYSA-N 4-methoxybutyl 2-cyanoprop-2-enoate Chemical compound COCCCCOC(=O)C(=C)C#N BZWFBZZBLILDAC-UHFFFAOYSA-N 0.000 description 1
- HXERDUPKFIKFBM-UHFFFAOYSA-N 7-methyloctyl 2-cyanoprop-2-enoate Chemical compound CC(C)CCCCCCOC(=O)C(=C)C#N HXERDUPKFIKFBM-UHFFFAOYSA-N 0.000 description 1
- YMWFRHAHSVCARN-UHFFFAOYSA-N 8-methylnonyl 2-cyanoprop-2-enoate Chemical compound CC(C)CCCCCCCOC(=O)C(=C)C#N YMWFRHAHSVCARN-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 229920001450 Alpha-Cyclodextrin Polymers 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 229940043377 alpha-cyclodextrin Drugs 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- VRKSJXIKRFNNFZ-UHFFFAOYSA-N benzyl 2-cyanoprop-2-enoate Chemical compound N#CC(=C)C(=O)OCC1=CC=CC=C1 VRKSJXIKRFNNFZ-UHFFFAOYSA-N 0.000 description 1
- WHGYBXFWUBPSRW-FOUAGVGXSA-N beta-cyclodextrin Chemical compound OC[C@H]([C@H]([C@@H]([C@H]1O)O)O[C@H]2O[C@@H]([C@@H](O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O3)[C@H](O)[C@H]2O)CO)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H]3O[C@@H]1CO WHGYBXFWUBPSRW-FOUAGVGXSA-N 0.000 description 1
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- MHQAEUJLOHUGPD-UHFFFAOYSA-N but-2-enyl 2-cyanoprop-2-enoate Chemical compound CC=CCOC(=O)C(=C)C#N MHQAEUJLOHUGPD-UHFFFAOYSA-N 0.000 description 1
- UMSYVRSBTJYRNW-UHFFFAOYSA-N butoxymethyl 2-cyanoprop-2-enoate Chemical compound CCCCOCOC(=O)C(=C)C#N UMSYVRSBTJYRNW-UHFFFAOYSA-N 0.000 description 1
- YZFWTZACSRHJQD-UHFFFAOYSA-N ciglitazone Chemical compound C=1C=C(CC2C(NC(=O)S2)=O)C=CC=1OCC1(C)CCCCC1 YZFWTZACSRHJQD-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- NLCKLZIHJQEMCU-UHFFFAOYSA-N cyano prop-2-enoate Chemical class C=CC(=O)OC#N NLCKLZIHJQEMCU-UHFFFAOYSA-N 0.000 description 1
- ILRMPAUJTPZAIQ-UHFFFAOYSA-N cyclohexyl 2-cyanoprop-2-enoate Chemical compound N#CC(=C)C(=O)OC1CCCCC1 ILRMPAUJTPZAIQ-UHFFFAOYSA-N 0.000 description 1
- RFKRFZSVPNPRQQ-UHFFFAOYSA-N cyclohexylmethyl 2-cyanoprop-2-enoate Chemical compound C(#N)C(C(=O)OCC1CCCCC1)=C RFKRFZSVPNPRQQ-UHFFFAOYSA-N 0.000 description 1
- KWKVJEUILVQMRR-UHFFFAOYSA-N decyl 2-cyanoprop-2-enoate Chemical compound CCCCCCCCCCOC(=O)C(=C)C#N KWKVJEUILVQMRR-UHFFFAOYSA-N 0.000 description 1
- LFJLAWZRNOKTDN-UHFFFAOYSA-N dodecyl 2-cyanoprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(=C)C#N LFJLAWZRNOKTDN-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- JJJFUHOGVZWXNQ-UHFFFAOYSA-N enbucrilate Chemical compound CCCCOC(=O)C(=C)C#N JJJFUHOGVZWXNQ-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
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- GDSRMADSINPKSL-HSEONFRVSA-N gamma-cyclodextrin Chemical compound OC[C@H]([C@H]([C@@H]([C@H]1O)O)O[C@H]2O[C@@H]([C@@H](O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O3)[C@H](O)[C@H]2O)CO)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H]3O[C@@H]1CO GDSRMADSINPKSL-HSEONFRVSA-N 0.000 description 1
- 229940080345 gamma-cyclodextrin Drugs 0.000 description 1
- 239000003349 gelling agent Substances 0.000 description 1
- WVXQYJXDTJWWEA-UHFFFAOYSA-N heptyl 2-cyanoprop-2-enoate Chemical compound CCCCCCCOC(=O)C(=C)C#N WVXQYJXDTJWWEA-UHFFFAOYSA-N 0.000 description 1
- XDZLHTBOHLGGCJ-UHFFFAOYSA-N hexyl 2-cyanoprop-2-enoate Chemical compound CCCCCCOC(=O)C(=C)C#N XDZLHTBOHLGGCJ-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- QRWOVIRDHQJFDB-UHFFFAOYSA-N isobutyl cyanoacrylate Chemical compound CC(C)COC(=O)C(=C)C#N QRWOVIRDHQJFDB-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M methacrylate group Chemical group C(C(=C)C)(=O)[O-] CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- WAYUQIGSHZZMTP-UHFFFAOYSA-N methyl 2-cyanoprop-2-eneperoxoate Chemical compound COOC(=O)C(=C)C#N WAYUQIGSHZZMTP-UHFFFAOYSA-N 0.000 description 1
- -1 naphthyl cyanoacrylate Chemical compound 0.000 description 1
- GQCBFHBKISYEQQ-UHFFFAOYSA-N nonyl 2-cyanoprop-2-enoate Chemical compound CCCCCCCCCOC(=O)C(=C)C#N GQCBFHBKISYEQQ-UHFFFAOYSA-N 0.000 description 1
- 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
- SBPXGLQYUALAQV-UHFFFAOYSA-N pentan-2-yl 2-cyanoprop-2-enoate Chemical compound CCCC(C)OC(=O)C(=C)C#N SBPXGLQYUALAQV-UHFFFAOYSA-N 0.000 description 1
- CMYFXTNUSQPQNH-UHFFFAOYSA-N pentan-3-yl 2-cyanoprop-2-enoate Chemical compound CCC(CC)OC(=O)C(=C)C#N CMYFXTNUSQPQNH-UHFFFAOYSA-N 0.000 description 1
- SXRFXXNXVPFXDU-UHFFFAOYSA-N pentyl 2-cyanoprop-2-enoate Chemical compound CCCCCOC(=O)C(=C)C#N SXRFXXNXVPFXDU-UHFFFAOYSA-N 0.000 description 1
- IPDQIHIYQHAUCO-UHFFFAOYSA-N phenyl 2-cyanoprop-2-enoate Chemical compound N#CC(=C)C(=O)OC1=CC=CC=C1 IPDQIHIYQHAUCO-UHFFFAOYSA-N 0.000 description 1
- 239000012994 photoredox catalyst Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 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 1
- UVTYYXOSOUBFIW-UHFFFAOYSA-N prop-2-ynyl 2-cyanoprop-2-enoate Chemical compound N#CC(=C)C(=O)OCC#C UVTYYXOSOUBFIW-UHFFFAOYSA-N 0.000 description 1
- VQRDNGVJZDEMHO-UHFFFAOYSA-N propoxymethyl 2-cyanoprop-2-enoate Chemical compound CCCOCOC(=O)C(=C)C#N VQRDNGVJZDEMHO-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance 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
- 238000003878 thermal aging Methods 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- GCSWIIQKEVHVMJ-UHFFFAOYSA-N undecyl 2-cyanoprop-2-enoate Chemical compound CCCCCCCCCCCOC(=O)C(=C)C#N GCSWIIQKEVHVMJ-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/11—Esters; Ether-esters of acyclic polycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L3/00—Compositions of starch, amylose or amylopectin or of their derivatives or degradation products
- C08L3/02—Starch; Degradation products thereof, e.g. dextrin
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
- C09J133/04—Homopolymers or copolymers of esters
- C09J133/14—Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur or oxygen atoms in addition to the carboxy oxygen
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J4/00—Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; adhesives, based on monomers of macromolecular compounds of groups C09J183/00 - C09J183/16
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L5/00—Compositions of polysaccharides or of their derivatives not provided for in groups C08L1/00 or C08L3/00
- C08L5/16—Cyclodextrin; Derivatives thereof
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
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Description
シアノアクリレート組成物を、以下の表1に記載の構成物質から、示された量で調製した。比較のため、LOCTITE 401、LOCTITE 435およびLOCTITE 4851も表に含めた。
Claims (13)
- (a)エチル−2−シアノアクリレートおよび20重量パーセントから45重量パーセントの量のオクチル−2−シアノアクリレートの混合物を含むシアノアクリレート成分、ならびに
(b)5重量パーセントから15重量パーセント未満の量のアセチルトリエチルシトレート
を含むシアノアクリレート組成物。 - 安定化量の酸性安定剤およ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。
- 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、エトキシ化ヒドロキシ化合物およびそれらの組み合わせからなる群より選択される、請求項3に記載の組成物。
- クラウンエーテルが15−クラウン−5、18−クラウン−6、ジベンゾ−18−クラウン−6、ベンゾ−15−クラウン−5−ジベンゾ−24−クラウン−8、ジベンゾ−30−クラウン−10、トリベンゾ−18−クラウン−6、asym−ジベンゾ−22−クラウン−6、ジベンゾ−14−クラウン−4、ジシクロヘキシル−18−クラウン−6、ジシクロヘキシル−24−クラウン−8、シクロヘキシル−12−クラウン−4、1,2−デカリル−15−クラウン−5、1,2−ナフト−15−クラウン−5、3,4,5−ナフチル−16−クラウン−5、1,2−メチル−ベンゾ−18−クラウン−6、1,2−メチルベンゾ−5、6−メチルベンゾ−18−クラウン−6、1,2−t−ブチル−18−クラウン−6、1,2−ビニルベンゾ−15−クラウン−5、1,2−ビニルベンゾ−18−クラウン−6、1,2−t−ブチル−シクロヘキシル−18−クラウン−6、asym−ジベンゾ−22−クラウン−6、および1,2−ベンゾ−1,4−ベンゾ−5−オキシゲン−20−クラウン−7およびそれらの組み合わせからなる群内の要素から選択される、請求項4に記載の組成物。
- 強化剤、耐衝撃添加剤、チキソトロピー付与剤、増粘剤、色素およびそれらの組み合わせからなる群より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。
- 少なくとも一方が熱可塑性材料から成る2つの基材を互いに接着する方法であって、
少なくとも1つの基材に、請求項1に記載のシアノアクリレート組成物を塗布するステップと、
接着剤が硬化するのに十分な時間、基材を互いに合わせるステップと、
を含む方法。 - シアノアクリレート組成物の硬化物に、改善された耐ねじり応力性を付与する方法であって、
エチル−2−シアノアクリレートおよび20重量パーセントから45重量パーセントの量のオクチル−2−シアノアクリレートの混合物を含むシアノアクリレート成分を用意するステップと、
そこへ、5重量パーセントから15重量パーセント未満の量のアセチルトリエチルシトレートを供給・混合して、シアノアクリレート組成物を形成するステップと、
合わせることが可能な表面を有する2つ以上の基材を用意し、その後、少なくとも一方が熱可塑性材料から成る基材の合わせることが可能な表面を、その間のシアノアクリレート組成物と共に合わせてアセンブリを形成するステップと、
を含む方法。 - アセチルトリエチルシトレートが5重量パーセントから12重量パーセントの量で存在する、請求項1に記載の組成物。
- オクチルシアノアクリレートおよびアセチルトリエチルシトレートが、合わせて30重量パーセントから65重量パーセントの範囲内の量で存在する、請求項1に記載の組成物。
- オクチルシアノアクリレートおよびアセチルトリエチルシトレートが、合わせて40重量パーセントから55重量パーセントの範囲内の量で存在する、請求項1に記載の組成物。
- シアノアクリレート成分の量が85重量パーセント超から95重量パーセントである、請求項1に記載の組成物。
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US201361825766P | 2013-05-21 | 2013-05-21 | |
US61/825,766 | 2013-05-21 | ||
PCT/US2014/038797 WO2014189938A1 (en) | 2013-05-21 | 2014-05-20 | Cyanoacrylate compositions |
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JP2016521773A JP2016521773A (ja) | 2016-07-25 |
JP6461924B2 true JP6461924B2 (ja) | 2019-01-30 |
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US (1) | US9528034B2 (ja) |
EP (1) | EP2999689B1 (ja) |
JP (1) | JP6461924B2 (ja) |
KR (1) | KR102063507B1 (ja) |
CN (1) | CN105246872B (ja) |
ES (1) | ES2651855T3 (ja) |
WO (1) | WO2014189938A1 (ja) |
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JP7293584B2 (ja) * | 2018-07-18 | 2023-06-20 | 東亞合成株式会社 | 2-シアノアクリレート系接着剤組成物 |
GB2576704B (en) * | 2018-08-16 | 2022-01-12 | Henkel IP & Holding GmbH | Cyanoacrylate compositions |
WO2020206405A1 (en) * | 2019-04-04 | 2020-10-08 | Henkel IP & Holding GmbH | Flexible photocurable cyanoacrylate compositions |
CN112680120B (zh) * | 2020-12-31 | 2022-05-17 | 杭州电子科技大学 | 一种光学元件加工用材料及其制备方法 |
KR102237285B1 (ko) * | 2021-01-29 | 2021-04-07 | 이혜경 | 안전성이 개선된 미용 접착제 조성물 및 이의 제조방법 |
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CN105246872A (zh) | 2016-01-13 |
WO2014189938A1 (en) | 2014-11-27 |
KR20160009024A (ko) | 2016-01-25 |
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US20160017189A1 (en) | 2016-01-21 |
EP2999689A1 (en) | 2016-03-30 |
ES2651855T3 (es) | 2018-01-30 |
JP2016521773A (ja) | 2016-07-25 |
EP2999689A4 (en) | 2016-10-05 |
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