JP2015224277A - 2−シアノアクリレート系接着剤用プライマー - Google Patents
2−シアノアクリレート系接着剤用プライマー Download PDFInfo
- Publication number
- JP2015224277A JP2015224277A JP2014109009A JP2014109009A JP2015224277A JP 2015224277 A JP2015224277 A JP 2015224277A JP 2014109009 A JP2014109009 A JP 2014109009A JP 2014109009 A JP2014109009 A JP 2014109009A JP 2015224277 A JP2015224277 A JP 2015224277A
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- Japan
- Prior art keywords
- primer
- cyanoacrylate
- cation
- formula
- alkyl group
- 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.)
- Granted
Links
- IJVRPNIWWODHHA-UHFFFAOYSA-N 2-cyanoprop-2-enoic acid Chemical compound OC(=O)C(=C)C#N IJVRPNIWWODHHA-UHFFFAOYSA-N 0.000 title claims abstract description 61
- 239000000853 adhesive Substances 0.000 title abstract description 22
- 230000001070 adhesive effect Effects 0.000 title abstract description 20
- 150000003839 salts Chemical class 0.000 claims abstract description 43
- -1 polypropylene Polymers 0.000 claims abstract description 33
- 150000001450 anions Chemical class 0.000 claims abstract description 13
- 150000001768 cations Chemical class 0.000 claims abstract description 12
- 238000002844 melting Methods 0.000 claims abstract description 8
- 230000008018 melting Effects 0.000 claims abstract description 8
- 239000004830 Super Glue Substances 0.000 claims description 52
- 125000000217 alkyl group Chemical group 0.000 claims description 22
- 125000004432 carbon atom Chemical group C* 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 17
- ZXMGHDIOOHOAAE-UHFFFAOYSA-N 1,1,1-trifluoro-n-(trifluoromethylsulfonyl)methanesulfonamide Chemical compound FC(F)(F)S(=O)(=O)NS(=O)(=O)C(F)(F)F ZXMGHDIOOHOAAE-UHFFFAOYSA-N 0.000 claims description 15
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 15
- 239000003960 organic solvent Substances 0.000 claims description 15
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical compound C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 claims description 11
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 claims description 9
- 150000003949 imides Chemical class 0.000 claims description 7
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims description 7
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 claims description 6
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 claims description 6
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical group C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 4
- 150000001298 alcohols Chemical class 0.000 claims description 4
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 4
- 150000002576 ketones Chemical class 0.000 claims description 4
- 125000003386 piperidinyl group Chemical group 0.000 claims description 4
- 125000004434 sulfur atom Chemical group 0.000 claims description 4
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 claims description 3
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 12
- 239000000463 material Substances 0.000 abstract description 11
- 239000004743 Polypropylene Substances 0.000 abstract description 10
- 229920001155 polypropylene Polymers 0.000 abstract description 10
- 239000004698 Polyethylene Substances 0.000 abstract description 8
- 229920000573 polyethylene Polymers 0.000 abstract description 8
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 abstract description 6
- 229910052731 fluorine Inorganic materials 0.000 abstract description 6
- 239000011737 fluorine Substances 0.000 abstract description 6
- 229920000098 polyolefin Polymers 0.000 abstract description 5
- 229920006324 polyoxymethylene Polymers 0.000 abstract description 5
- 229920005989 resin Polymers 0.000 abstract description 5
- 239000011347 resin Substances 0.000 abstract description 5
- 229930182556 Polyacetal Natural products 0.000 abstract description 3
- 229920001887 crystalline plastic Polymers 0.000 abstract description 3
- 230000002688 persistence Effects 0.000 abstract 1
- 238000000034 method Methods 0.000 description 11
- 229920001971 elastomer Polymers 0.000 description 9
- 239000000806 elastomer Substances 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- ZUZLIXGTXQBUDC-UHFFFAOYSA-N methyltrioctylammonium Chemical compound CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC ZUZLIXGTXQBUDC-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 229920001707 polybutylene terephthalate Polymers 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- XLJSMWDFUFADIA-UHFFFAOYSA-N 1,3-diethylimidazol-1-ium Chemical compound CCN1C=C[N+](CC)=C1 XLJSMWDFUFADIA-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- FGBJXOREULPLGL-UHFFFAOYSA-N ethyl cyanoacrylate Chemical compound CCOC(=O)C(=C)C#N FGBJXOREULPLGL-UHFFFAOYSA-N 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 description 3
- RVEJOWGVUQQIIZ-UHFFFAOYSA-N 1-hexyl-3-methylimidazolium Chemical compound CCCCCCN1C=C[N+](C)=C1 RVEJOWGVUQQIIZ-UHFFFAOYSA-N 0.000 description 2
- AMKUSFIBHAUBIJ-UHFFFAOYSA-N 1-hexylpyridin-1-ium Chemical compound CCCCCC[N+]1=CC=CC=C1 AMKUSFIBHAUBIJ-UHFFFAOYSA-N 0.000 description 2
- LSFWFJFDPRFPBK-UHFFFAOYSA-N 1-methyl-3-pentylimidazol-1-ium Chemical compound CCCCCN1C=C[N+](C)=C1 LSFWFJFDPRFPBK-UHFFFAOYSA-N 0.000 description 2
- WVDDUSFOSWWJJH-UHFFFAOYSA-N 1-methyl-3-propylimidazol-1-ium Chemical compound CCCN1C=C[N+](C)=C1 WVDDUSFOSWWJJH-UHFFFAOYSA-N 0.000 description 2
- HOZSKYZXBJWURK-UHFFFAOYSA-N 1-pentylpyridin-1-ium Chemical compound CCCCC[N+]1=CC=CC=C1 HOZSKYZXBJWURK-UHFFFAOYSA-N 0.000 description 2
- OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-dimethylpyridine Chemical compound CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Natural products CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000012790 confirmation Methods 0.000 description 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
- OGQYPPBGSLZBEG-UHFFFAOYSA-N dimethyl(dioctadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC OGQYPPBGSLZBEG-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
- WFIYFFUAOQKJJS-UHFFFAOYSA-N tetraoctylphosphanium Chemical compound CCCCCCCC[P+](CCCCCCCC)(CCCCCCCC)CCCCCCCC WFIYFFUAOQKJJS-UHFFFAOYSA-N 0.000 description 2
- SNDRYHUSDCHSDJ-UHFFFAOYSA-N tributyl(dodecyl)phosphanium Chemical compound CCCCCCCCCCCC[P+](CCCC)(CCCC)CCCC SNDRYHUSDCHSDJ-UHFFFAOYSA-N 0.000 description 2
- KLNYRFBLEYSXHW-UHFFFAOYSA-N 1,2-diethylpyridin-1-ium Chemical compound CCC1=CC=CC=[N+]1CC KLNYRFBLEYSXHW-UHFFFAOYSA-N 0.000 description 1
- UMZDENILBZKMFY-UHFFFAOYSA-N 1,2-dimethylpyridin-1-ium Chemical compound CC1=CC=CC=[N+]1C UMZDENILBZKMFY-UHFFFAOYSA-N 0.000 description 1
- FCVKBWXKTRJXTQ-UHFFFAOYSA-N 1,3-diethylpyridin-1-ium Chemical compound CCC1=CC=C[N+](CC)=C1 FCVKBWXKTRJXTQ-UHFFFAOYSA-N 0.000 description 1
- HVVRUQBMAZRKPJ-UHFFFAOYSA-N 1,3-dimethylimidazolium Chemical compound CN1C=C[N+](C)=C1 HVVRUQBMAZRKPJ-UHFFFAOYSA-N 0.000 description 1
- MPUIJCPHOVBPOB-UHFFFAOYSA-N 1,3-dimethylpyridin-1-ium Chemical compound CC1=CC=C[N+](C)=C1 MPUIJCPHOVBPOB-UHFFFAOYSA-N 0.000 description 1
- IZPNVUYQWBZYEA-UHFFFAOYSA-N 1,4-dimethylpyridin-1-ium Chemical compound CC1=CC=[N+](C)C=C1 IZPNVUYQWBZYEA-UHFFFAOYSA-N 0.000 description 1
- IQQRAVYLUAZUGX-UHFFFAOYSA-N 1-butyl-3-methylimidazolium Chemical compound CCCCN1C=C[N+](C)=C1 IQQRAVYLUAZUGX-UHFFFAOYSA-N 0.000 description 1
- REACWASHYHDPSQ-UHFFFAOYSA-N 1-butylpyridin-1-ium Chemical compound CCCC[N+]1=CC=CC=C1 REACWASHYHDPSQ-UHFFFAOYSA-N 0.000 description 1
- MFMBELVKZWEQOM-UHFFFAOYSA-N 1-decylpyridin-1-ium Chemical compound CCCCCCCCCC[N+]1=CC=CC=C1 MFMBELVKZWEQOM-UHFFFAOYSA-N 0.000 description 1
- QHTSJPCQUQAHSQ-UHFFFAOYSA-M 1-dodecylpyridin-1-ium thiocyanate Chemical compound [S-]C#N.C(CCCCCCCCCCC)[N+]1=CC=CC=C1 QHTSJPCQUQAHSQ-UHFFFAOYSA-M 0.000 description 1
- FUZQTBHDJAOMJB-UHFFFAOYSA-N 1-ethyl-2-methylpyridin-1-ium Chemical compound CC[N+]1=CC=CC=C1C FUZQTBHDJAOMJB-UHFFFAOYSA-N 0.000 description 1
- NJMWOUFKYKNWDW-UHFFFAOYSA-N 1-ethyl-3-methylimidazolium Chemical compound CCN1C=C[N+](C)=C1 NJMWOUFKYKNWDW-UHFFFAOYSA-N 0.000 description 1
- REITYCXGQIGALX-UHFFFAOYSA-N 1-ethyl-3-methylpyridin-1-ium Chemical compound CC[N+]1=CC=CC(C)=C1 REITYCXGQIGALX-UHFFFAOYSA-N 0.000 description 1
- WMHWQEPQRZIOCT-UHFFFAOYSA-N 1-ethyl-4-methylpyridin-1-ium Chemical compound CC[N+]1=CC=C(C)C=C1 WMHWQEPQRZIOCT-UHFFFAOYSA-N 0.000 description 1
- OIDIRWZVUWCCCO-UHFFFAOYSA-N 1-ethylpyridin-1-ium Chemical compound CC[N+]1=CC=CC=C1 OIDIRWZVUWCCCO-UHFFFAOYSA-N 0.000 description 1
- BOFYFGANDNPXEM-UHFFFAOYSA-N 1-heptylpyridin-1-ium Chemical compound CCCCCCC[N+]1=CC=CC=C1 BOFYFGANDNPXEM-UHFFFAOYSA-N 0.000 description 1
- KVUBRTKSOZFXGX-UHFFFAOYSA-N 1-hexyl-4-methylpyridin-1-ium Chemical compound CCCCCC[N+]1=CC=C(C)C=C1 KVUBRTKSOZFXGX-UHFFFAOYSA-N 0.000 description 1
- PLZKUGNPZXCRBY-UHFFFAOYSA-N 1-nonylpyridin-1-ium Chemical compound CCCCCCCCC[N+]1=CC=CC=C1 PLZKUGNPZXCRBY-UHFFFAOYSA-N 0.000 description 1
- XDEQOBPALZZTCA-UHFFFAOYSA-N 1-octylpyridin-1-ium Chemical compound CCCCCCCC[N+]1=CC=CC=C1 XDEQOBPALZZTCA-UHFFFAOYSA-N 0.000 description 1
- CRTKBIFIDSNKCN-UHFFFAOYSA-N 1-propylpyridin-1-ium Chemical compound CCC[N+]1=CC=CC=C1 CRTKBIFIDSNKCN-UHFFFAOYSA-N 0.000 description 1
- BJMBCVIFMXOIIH-UHFFFAOYSA-N 2-ethyl-1-methylpyridin-1-ium Chemical compound CCC1=CC=CC=[N+]1C BJMBCVIFMXOIIH-UHFFFAOYSA-N 0.000 description 1
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- OLOJVDZXVFIAFJ-UHFFFAOYSA-N 3-ethyl-1-methylpyridin-1-ium Chemical compound CCC1=CC=C[N+](C)=C1 OLOJVDZXVFIAFJ-UHFFFAOYSA-N 0.000 description 1
- JIGUICYYOYEXFS-UHFFFAOYSA-N 3-tert-butylbenzene-1,2-diol Chemical compound CC(C)(C)C1=CC=CC(O)=C1O JIGUICYYOYEXFS-UHFFFAOYSA-N 0.000 description 1
- JMWUAFSVHRBNNW-UHFFFAOYSA-N 4-ethyl-1-methylpyridin-1-ium Chemical compound CCC1=CC=[N+](C)C=C1 JMWUAFSVHRBNNW-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical compound FB(F)F.CCOCC KZMGYPLQYOPHEL-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- YYLLIJHXUHJATK-UHFFFAOYSA-N Cyclohexyl acetate Chemical compound CC(=O)OC1CCCCC1 YYLLIJHXUHJATK-UHFFFAOYSA-N 0.000 description 1
- JGFDZZLUDWMUQH-UHFFFAOYSA-N Didecyldimethylammonium Chemical compound CCCCCCCCCC[N+](C)(C)CCCCCCCCCC JGFDZZLUDWMUQH-UHFFFAOYSA-N 0.000 description 1
- ZVFDTKUVRCTHQE-UHFFFAOYSA-N Diisodecyl phthalate Chemical compound CC(C)CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC(C)C ZVFDTKUVRCTHQE-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- AFVFQIVMOAPDHO-UHFFFAOYSA-M Methanesulfonate Chemical group CS([O-])(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-M 0.000 description 1
- MWCLLHOVUTZFKS-UHFFFAOYSA-N Methyl cyanoacrylate Chemical compound COC(=O)C(=C)C#N MWCLLHOVUTZFKS-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- PQBAWAQIRZIWIV-UHFFFAOYSA-N N-methylpyridinium Chemical compound C[N+]1=CC=CC=C1 PQBAWAQIRZIWIV-UHFFFAOYSA-N 0.000 description 1
- GSBKRFGXEJLVMI-UHFFFAOYSA-N Nervonyl carnitine Chemical compound CCC[N+](C)(C)C GSBKRFGXEJLVMI-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- PLZVEHJLHYMBBY-UHFFFAOYSA-N Tetradecylamine Chemical compound CCCCCCCCCCCCCCN PLZVEHJLHYMBBY-UHFFFAOYSA-N 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- HEZJLLQLTPQSMT-UHFFFAOYSA-N acetic acid;1,2-diphenylethane-1,2-dione Chemical compound CC(O)=O.C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1 HEZJLLQLTPQSMT-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 238000010539 anionic addition polymerization reaction Methods 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- INDFXCHYORWHLQ-UHFFFAOYSA-N bis(trifluoromethylsulfonyl)azanide;1-butyl-3-methylimidazol-3-ium Chemical compound CCCCN1C=C[N+](C)=C1.FC(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F INDFXCHYORWHLQ-UHFFFAOYSA-N 0.000 description 1
- XHIHMDHAPXMAQK-UHFFFAOYSA-N bis(trifluoromethylsulfonyl)azanide;1-butylpyridin-1-ium Chemical compound CCCC[N+]1=CC=CC=C1.FC(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F XHIHMDHAPXMAQK-UHFFFAOYSA-N 0.000 description 1
- LRESCJAINPKJTO-UHFFFAOYSA-N bis(trifluoromethylsulfonyl)azanide;1-ethyl-3-methylimidazol-3-ium Chemical compound CCN1C=C[N+](C)=C1.FC(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F LRESCJAINPKJTO-UHFFFAOYSA-N 0.000 description 1
- SLEKRZBYCSJUNO-UHFFFAOYSA-N bis(trifluoromethylsulfonyl)azanide;hexyl(trimethyl)azanium Chemical compound CCCCCC[N+](C)(C)C.FC(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F SLEKRZBYCSJUNO-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 150000003983 crown ethers Chemical class 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- BGIWPLZAYSSXPH-UHFFFAOYSA-N decyl(triheptyl)phosphanium Chemical compound CCCCCCCCCC[P+](CCCCCCC)(CCCCCCC)CCCCCCC BGIWPLZAYSSXPH-UHFFFAOYSA-N 0.000 description 1
- IACLCJVNAROMPM-UHFFFAOYSA-N decyl(tripentyl)phosphanium Chemical compound CCCCCCCCCC[P+](CCCCC)(CCCCC)CCCCC IACLCJVNAROMPM-UHFFFAOYSA-N 0.000 description 1
- VQNIOZLNRYKVEF-UHFFFAOYSA-N decylphosphane Chemical compound CCCCCCCCCCP VQNIOZLNRYKVEF-UHFFFAOYSA-N 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 229940078672 didecyldimethylammonium Drugs 0.000 description 1
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 1
- 229960001826 dimethylphthalate Drugs 0.000 description 1
- HPYNZHMRTTWQTB-UHFFFAOYSA-N dimethylpyridine Natural products CC1=CC=CN=C1C HPYNZHMRTTWQTB-UHFFFAOYSA-N 0.000 description 1
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- RYQKCWVYSTXPAY-UHFFFAOYSA-N dodecyl(triheptyl)phosphanium Chemical compound CCCCCCCCCCCC[P+](CCCCCCC)(CCCCCCC)CCCCCCC RYQKCWVYSTXPAY-UHFFFAOYSA-N 0.000 description 1
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- 229910052739 hydrogen Inorganic materials 0.000 description 1
- KIWOEMYWJYYRNL-UHFFFAOYSA-N icosyl(trioctyl)phosphanium Chemical compound C(CCCCCCC)[P+](CCCCCCCCCCCCCCCCCCCC)(CCCCCCCC)CCCCCCCC KIWOEMYWJYYRNL-UHFFFAOYSA-N 0.000 description 1
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- 125000002883 imidazolyl group Chemical group 0.000 description 1
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- 230000002045 lasting effect Effects 0.000 description 1
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- KTQDYGVEEFGIIL-UHFFFAOYSA-N n-fluorosulfonylsulfamoyl fluoride Chemical group FS(=O)(=O)NS(F)(=O)=O KTQDYGVEEFGIIL-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- TXBPMXYUBKFFDW-UHFFFAOYSA-N nonadecyl(trioctyl)phosphanium Chemical compound CCCCCCCCCCCCCCCCCCC[P+](CCCCCCCC)(CCCCCCCC)CCCCCCCC TXBPMXYUBKFFDW-UHFFFAOYSA-N 0.000 description 1
- XMSLFERHLXTWNP-UHFFFAOYSA-N nonadecyl(tripentyl)phosphanium Chemical compound CCCCCCCCCCCCCCCCCCC[P+](CCCCC)(CCCCC)CCCCC XMSLFERHLXTWNP-UHFFFAOYSA-N 0.000 description 1
- 230000000269 nucleophilic effect Effects 0.000 description 1
- WAVPCNDAVQRZJO-UHFFFAOYSA-N octadecyl(trioctyl)phosphanium Chemical compound CCCCCCCCCCCCCCCCCC[P+](CCCCCCCC)(CCCCCCCC)CCCCCCCC WAVPCNDAVQRZJO-UHFFFAOYSA-N 0.000 description 1
- LAJNKQFMFZUMJH-UHFFFAOYSA-N octadecyl(tripentyl)phosphanium Chemical compound CCCCCCCCCCCCCCCCCC[P+](CCCCC)(CCCCC)CCCCC LAJNKQFMFZUMJH-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- AZRYABPJLSBNIU-UHFFFAOYSA-N octyl(tripentyl)phosphanium Chemical compound CCCCCCCC[P+](CCCCC)(CCCCC)CCCCC AZRYABPJLSBNIU-UHFFFAOYSA-N 0.000 description 1
- VDDBYTZQROBWGY-UHFFFAOYSA-N octyl(tripropyl)phosphanium Chemical compound CCCCCCCC[P+](CCC)(CCC)CCC VDDBYTZQROBWGY-UHFFFAOYSA-N 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 1
- ZRCIEUCJKPUBRO-UHFFFAOYSA-N pentadecyl(tripentyl)phosphanium Chemical compound CCCCCCCCCCCCCCC[P+](CCCCC)(CCCCC)CCCCC ZRCIEUCJKPUBRO-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 150000004714 phosphonium salts Chemical class 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920003225 polyurethane elastomer Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- VWGARRKCFILYNY-UHFFFAOYSA-N tetra(nonyl)azanium Chemical compound CCCCCCCCC[N+](CCCCCCCCC)(CCCCCCCCC)CCCCCCCCC VWGARRKCFILYNY-UHFFFAOYSA-N 0.000 description 1
- WCKZOASXBBGEKB-UHFFFAOYSA-N tetra(nonyl)phosphanium Chemical compound CCCCCCCCC[P+](CCCCCCCCC)(CCCCCCCCC)CCCCCCCCC WCKZOASXBBGEKB-UHFFFAOYSA-N 0.000 description 1
- DAUOXRUBCACRRL-UHFFFAOYSA-N tetradecylphosphane Chemical compound CCCCCCCCCCCCCCP DAUOXRUBCACRRL-UHFFFAOYSA-N 0.000 description 1
- UOBBAWATEUXIQF-UHFFFAOYSA-N tetradodecylazanium Chemical compound CCCCCCCCCCCC[N+](CCCCCCCCCCCC)(CCCCCCCCCCCC)CCCCCCCCCCCC UOBBAWATEUXIQF-UHFFFAOYSA-N 0.000 description 1
- CHYBTAZWINMGHA-UHFFFAOYSA-N tetraoctylazanium Chemical compound CCCCCCCC[N+](CCCCCCCC)(CCCCCCCC)CCCCCCCC CHYBTAZWINMGHA-UHFFFAOYSA-N 0.000 description 1
- USFPINLPPFWTJW-UHFFFAOYSA-N tetraphenylphosphonium Chemical compound C1=CC=CC=C1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 USFPINLPPFWTJW-UHFFFAOYSA-N 0.000 description 1
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- SKWPRNVKIJEVCC-UHFFFAOYSA-N triheptyl(undecyl)phosphanium Chemical compound CCCCCCCCCCC[P+](CCCCCCC)(CCCCCCC)CCCCCCC SKWPRNVKIJEVCC-UHFFFAOYSA-N 0.000 description 1
- HSLJRXHBBJBJQS-UHFFFAOYSA-N trihexyl(tridecyl)phosphanium Chemical compound CCCCCCCCCCCCC[P+](CCCCCC)(CCCCCC)CCCCCC HSLJRXHBBJBJQS-UHFFFAOYSA-N 0.000 description 1
- LAGQNGWYNLUQRI-UHFFFAOYSA-N trioctylmethylammonium bis(trifluoromethylsulfonyl)imide Chemical compound FC(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F.CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC LAGQNGWYNLUQRI-UHFFFAOYSA-N 0.000 description 1
- SBRRUWARASWHKG-UHFFFAOYSA-N tripentyl(tetradecyl)phosphanium Chemical compound CCCCCCCCCCCCCC[P+](CCCCC)(CCCCC)CCCCC SBRRUWARASWHKG-UHFFFAOYSA-N 0.000 description 1
- ZYMUOGYKYFMPPF-UHFFFAOYSA-N tripentyl(tridecyl)phosphanium Chemical compound CCCCCCCCCCCCC[P+](CCCCC)(CCCCC)CCCCC ZYMUOGYKYFMPPF-UHFFFAOYSA-N 0.000 description 1
- KOUFMZLAXUENBY-UHFFFAOYSA-N tripentyl(undecyl)phosphanium Chemical compound CCCCCCCCCCC[P+](CCCCC)(CCCCC)CCCCC KOUFMZLAXUENBY-UHFFFAOYSA-N 0.000 description 1
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Abstract
Description
式(1)
前記カチオンがアンモニウムカチオン、ピリジニウムカチオン、イミダゾリウムカチオンまたはホスホニウムカチオンである〔1〕記載の2−シアノアクリレート系接着剤用プライマー。
前記アンモニウムカチオンが式(2)
で表されるアンモニウムカチオン、前記ピリジニウムカチオンが式(3)
で表されるホスホニウムカチオンである〔2〕記載の2−シアノアクリレート系接着剤用プライマー。
前記カチオンが前記式(2)で表されるアンモニウムカチオンである〔1〕記載の2−シアノアクリレート系接着剤用プライマー。
前記アニオンがS原子を含有するアニオンである〔1〕〜〔4〕のいずれか1つに記載の2−シアノアクリレート系接着剤用プライマー。
前記アニオンがチオシアネート、ビス(トリフルオロメタンスルホニル)イミド、ビス(フルオロメタンスルホニル)イミド、トリフルオロメタンスルホネートまたはp−トルエンスルホナートである〔1〕〜〔5〕のいずれか1つに記載の2−シアノアクリレート系接着剤用プライマー。
〔1〕〜〔6〕のいずれか1つに記載の2−シアノアクリレート系接着剤用プライマーの少なくとも1種と有機溶媒を含有してなる2−シアノアクリレート系接着剤用プライマー組成物。
前記有機溶媒が脂肪族炭化水素、芳香族炭化水素、エステル、ケトンおよびアルコールよりなる群より選ばれる少なくとも1種の有機溶媒である〔7〕記載の2−シアノアクリレート系接着剤用プライマー組成物。
〔1〕〜〔6〕のいずれか1つに記載のシアノアクリレート系接着剤用プライマーの少なくとも1種を0.01〜20重量%含有する〔7〕または〔8〕記載のシアノアクリレート系接着剤用プライマー組成物。
で表される融点が150℃以下のオニウム塩である。用いるオニウム塩の融点が150℃より高い場合、プライマーとしての効果が持続しないだけでなく、プライマーそのものの効果(難接着材に対する接着強度の向上)が発現しない等の問題がある。
で表されるアンモニウムカチオンが挙げられる。
で表されるホスホニウムカチオンが挙げられる。
下記方法によりプライマー組成物として調製する前のプライマーの臭気を確認した。
強い臭気あり・・・×、強い臭気なし・・・○
表1に示すオニウム塩および3級アミンを、表2〜5に示す濃度(重量%)となるよう、表2〜5に示す有機溶媒に加え、攪拌溶解して本発明のプライマー組成物を調製した。
JIS K−6861−6「引張剪断接着強さ測定方法」に準ずる方法により測定した。
(単位(N/mm2))
被着体としてポリブチレンテレフタレート(PBT)板、ポリプロピレン(PP)板およびポリエチレン(PE)板(2×25×50mm、エンジニアリングテストサービス社製)を用意し、PBT同士、PP同士、PE同士の接着試験を行った。具体的には、2枚同種の被着体の両表面に上述の方法で調製したプライマー組成物を塗布し、20℃の室内に10分間放置乾燥した後、2−シアノアクリレート系接着剤(シアノボンドRP−X;田岡化学工業株式会社製・エチル−2−シアノアクリレート))を片方の被着体のプライマー組成物を塗布した面に滴下し、2−シアノアクリレート系接着剤を25×12.5mmの面となるように塗り広げた後、被着体を貼り合せ、24時間養生後、引張剪断接着強さを測定した。結果を表2〜4に示す。なお、表中の「オープンタイム」とはプライマー組成物を塗布した後、2−シアノアクリレート系接着剤を滴下するまでの時間のことを表す。
また、特にオニウム塩のカチオンが前記式(2)で表される4級アンモニウムカチオンである場合(D、H)、その効果がより顕著であることが判明した。
被着体としてポリプロピレン(PP)板(2×25×50mm、エンジニアリングテストサービス社製)を使用し、オープンタイムを3時間とする以外は実施例1と同様に試験を行った。結果を表5に示す。(下記表におけるオープンタイム10分の引張剪断接着強さの値は上記実施例7、9、10、11、比較例8の値である。)
Claims (9)
- 前記カチオンがアンモニウムカチオン、ピリジニウムカチオン、イミダゾリウムカチオンまたはホスホニウムカチオンである請求項1記載の2−シアノアクリレート系接着剤用プライマー。
- 前記アンモニウムカチオンが式(2)
で表されるアンモニウムカチオン、前記ピリジニウムカチオンが式(3)
で表されるピリジニウムカチオン、前記イミダゾリウムカチオンが式(4)
で表されるイミダゾリウムカチオン、前記ホスホニウムカチオンが式(5)
で表されるホスホニウムカチオンである請求項2記載の2−シアノアクリレート系接着剤用プライマー。 - 前記カチオンが前記式(2)で表されるアンモニウムカチオンである請求項1記載の2−シアノアクリレート系接着剤用プライマー。
- 前記アニオンがS原子を含有するアニオンである請求項1〜4いずれか1項に記載の2−シアノアクリレート系接着剤用プライマー。
- 前記アニオンがチオシアネート、ビス(トリフルオロメタンスルホニル)イミド、ビス(フルオロメタンスルホニル)イミド、トリフルオロメタンスルホネートまたはp−トルエンスルホナートである請求項1〜5いずれか1項に記載の2−シアノアクリレート系接着剤用プライマー。
- 請求項1〜6いずれか1項に記載の2−シアノアクリレート系接着剤用プライマーの少なくとも1種と有機溶媒を含有してなる2−シアノアクリレート系接着剤用プライマー組成物。
- 前記有機溶媒が脂肪族炭化水素、芳香族炭化水素、エステル、ケトンおよびアルコールよりなる群より選ばれる少なくとも1種の有機溶媒である請求項7記載の2−シアノアクリレート系接着剤用プライマー組成物。
- 請求項1〜6いずれか1項に記載のシアノアクリレート系接着剤用プライマーの少なくとも1種を0.01〜20重量%含有する請求項7または8記載のシアノアクリレート系接着剤用プライマー組成物。
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Cited By (1)
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CN114686100A (zh) * | 2022-04-13 | 2022-07-01 | 宁波鑫智达新材料有限公司 | 瞬干胶底涂剂及其制备方法 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5086537A (ja) * | 1973-12-04 | 1975-07-11 | ||
JPS5889674A (ja) * | 1981-11-20 | 1983-05-28 | ミネソタ・マイニング・アンド・マニユフアクチユアリング・コンパニ− | 接着剤および接着法 |
JPH026577A (ja) * | 1988-03-16 | 1990-01-10 | Loctite Corp | プライマー組成物 |
WO2014042082A1 (ja) * | 2012-09-11 | 2014-03-20 | 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 |
WO2014091966A1 (ja) * | 2012-12-14 | 2014-06-19 | 東亞合成株式会社 | 接着剤組成物 |
-
2014
- 2014-05-27 JP JP2014109009A patent/JP6319897B2/ja active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5086537A (ja) * | 1973-12-04 | 1975-07-11 | ||
JPS5889674A (ja) * | 1981-11-20 | 1983-05-28 | ミネソタ・マイニング・アンド・マニユフアクチユアリング・コンパニ− | 接着剤および接着法 |
JPH026577A (ja) * | 1988-03-16 | 1990-01-10 | Loctite Corp | プライマー組成物 |
WO2014042082A1 (ja) * | 2012-09-11 | 2014-03-20 | 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 |
WO2014091966A1 (ja) * | 2012-12-14 | 2014-06-19 | 東亞合成株式会社 | 接着剤組成物 |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114686100A (zh) * | 2022-04-13 | 2022-07-01 | 宁波鑫智达新材料有限公司 | 瞬干胶底涂剂及其制备方法 |
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