JP2016094566A - Adhesive composition - Google Patents
Adhesive composition Download PDFInfo
- Publication number
- JP2016094566A JP2016094566A JP2014232540A JP2014232540A JP2016094566A JP 2016094566 A JP2016094566 A JP 2016094566A JP 2014232540 A JP2014232540 A JP 2014232540A JP 2014232540 A JP2014232540 A JP 2014232540A JP 2016094566 A JP2016094566 A JP 2016094566A
- Authority
- JP
- Japan
- Prior art keywords
- group
- polyolefin
- manufactured
- composition
- polymer
- 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
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- 239000000203 mixture Substances 0.000 title claims abstract description 55
- 239000000853 adhesive Substances 0.000 title claims abstract description 28
- 230000001070 adhesive effect Effects 0.000 title claims abstract description 28
- 229920000098 polyolefin Polymers 0.000 claims abstract description 40
- 229920000642 polymer Polymers 0.000 claims abstract description 29
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 24
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000000460 chlorine Substances 0.000 claims abstract description 11
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 11
- 238000002844 melting Methods 0.000 claims abstract description 8
- 230000008018 melting Effects 0.000 claims abstract description 8
- -1 methyldimethoxysilyl group Chemical group 0.000 claims description 56
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 239000000758 substrate Substances 0.000 abstract description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 26
- 239000004743 Polypropylene Substances 0.000 description 26
- 229920001155 polypropylene Polymers 0.000 description 26
- 238000000034 method Methods 0.000 description 13
- 229910000019 calcium carbonate Inorganic materials 0.000 description 11
- 125000005702 oxyalkylene group Chemical group 0.000 description 11
- 239000002994 raw material Substances 0.000 description 10
- 239000007795 chemical reaction product Substances 0.000 description 8
- 229920002725 thermoplastic elastomer Polymers 0.000 description 8
- CNPVJWYWYZMPDS-UHFFFAOYSA-N 2-methyldecane Chemical compound CCCCCCCCC(C)C CNPVJWYWYZMPDS-UHFFFAOYSA-N 0.000 description 7
- 239000002202 Polyethylene glycol Substances 0.000 description 7
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 7
- 229920001223 polyethylene glycol Polymers 0.000 description 7
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- 229920002050 silicone resin Polymers 0.000 description 7
- HEXHLHNCJVXPNU-UHFFFAOYSA-N 2-(trimethoxysilylmethyl)butane-1,4-diamine Chemical compound CO[Si](OC)(OC)CC(CN)CCN HEXHLHNCJVXPNU-UHFFFAOYSA-N 0.000 description 6
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 6
- IJKVHSBPTUYDLN-UHFFFAOYSA-N dihydroxy(oxo)silane Chemical compound O[Si](O)=O IJKVHSBPTUYDLN-UHFFFAOYSA-N 0.000 description 6
- 239000000945 filler Substances 0.000 description 6
- 229920002554 vinyl polymer Polymers 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 5
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 239000003208 petroleum Substances 0.000 description 4
- 239000004014 plasticizer Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 3
- 235000013312 flour Nutrition 0.000 description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 150000007934 α,β-unsaturated carboxylic acids Chemical class 0.000 description 3
- RSWGJHLUYNHPMX-UHFFFAOYSA-N 1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid Chemical compound C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical compound CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 description 2
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-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
- 239000004593 Epoxy Substances 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 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
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000012024 dehydrating agents Substances 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 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
- 150000002009 diols Chemical class 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000001298 n-hexoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 2
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
- 125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 2
- 229920000193 polymethacrylate Polymers 0.000 description 2
- 229920006124 polyolefin elastomer Polymers 0.000 description 2
- 229920005672 polyolefin resin Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 125000005369 trialkoxysilyl group Chemical group 0.000 description 2
- PZJJKWKADRNWSW-UHFFFAOYSA-N trimethoxysilicon Chemical group CO[Si](OC)OC PZJJKWKADRNWSW-UHFFFAOYSA-N 0.000 description 2
- 239000004711 α-olefin Substances 0.000 description 2
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- YEVQZPWSVWZAOB-UHFFFAOYSA-N 2-(bromomethyl)-1-iodo-4-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC=C(I)C(CBr)=C1 YEVQZPWSVWZAOB-UHFFFAOYSA-N 0.000 description 1
- IHCCLXNEEPMSIO-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperidin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 IHCCLXNEEPMSIO-UHFFFAOYSA-N 0.000 description 1
- AYKYXWQEBUNJCN-UHFFFAOYSA-N 3-methylfuran-2,5-dione Chemical compound CC1=CC(=O)OC1=O AYKYXWQEBUNJCN-UHFFFAOYSA-N 0.000 description 1
- OFNISBHGPNMTMS-UHFFFAOYSA-N 3-methylideneoxolane-2,5-dione Chemical compound C=C1CC(=O)OC1=O OFNISBHGPNMTMS-UHFFFAOYSA-N 0.000 description 1
- DFGKGUXTPFWHIX-UHFFFAOYSA-N 6-[2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]acetyl]-3H-1,3-benzoxazol-2-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)C1=CC2=C(NC(O2)=O)C=C1 DFGKGUXTPFWHIX-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- MHZGKXUYDGKKIU-UHFFFAOYSA-N Decylamine Chemical compound CCCCCCCCCCN MHZGKXUYDGKKIU-UHFFFAOYSA-N 0.000 description 1
- IEPRKVQEAMIZSS-UHFFFAOYSA-N Di-Et ester-Fumaric acid Natural products CCOC(=O)C=CC(=O)OCC IEPRKVQEAMIZSS-UHFFFAOYSA-N 0.000 description 1
- PYGXAGIECVVIOZ-UHFFFAOYSA-N Dibutyl decanedioate Chemical compound CCCCOC(=O)CCCCCCCCC(=O)OCCCC PYGXAGIECVVIOZ-UHFFFAOYSA-N 0.000 description 1
- IEPRKVQEAMIZSS-WAYWQWQTSA-N Diethyl maleate Chemical compound CCOC(=O)\C=C/C(=O)OCC IEPRKVQEAMIZSS-WAYWQWQTSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 240000007049 Juglans regia Species 0.000 description 1
- 235000009496 Juglans regia Nutrition 0.000 description 1
- 229920000271 Kevlar® Polymers 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 229920004482 WACKER® Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000005370 alkoxysilyl group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 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
- 230000001588 bifunctional effect Effects 0.000 description 1
- ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 description 1
- BQSLMFSQEBXZHN-UHFFFAOYSA-N bis(8-methylnonyl) butanedioate Chemical compound CC(C)CCCCCCCOC(=O)CCC(=O)OCCCCCCCC(C)C BQSLMFSQEBXZHN-UHFFFAOYSA-N 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
- 229940018557 citraconic acid Drugs 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- JJQZDUKDJDQPMQ-UHFFFAOYSA-N dimethoxy(dimethyl)silane Chemical compound CO[Si](C)(C)OC JJQZDUKDJDQPMQ-UHFFFAOYSA-N 0.000 description 1
- LDCRTTXIJACKKU-ARJAWSKDSA-N dimethyl maleate Chemical compound COC(=O)\C=C/C(=O)OC LDCRTTXIJACKKU-ARJAWSKDSA-N 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
- TVWTZAGVNBPXHU-FOCLMDBBSA-N dioctyl (e)-but-2-enedioate Chemical compound CCCCCCCCOC(=O)\C=C\C(=O)OCCCCCCCC TVWTZAGVNBPXHU-FOCLMDBBSA-N 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 229920006351 engineering plastic Polymers 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002169 ethanolamines Chemical class 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000012765 fibrous filler Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 238000010559 graft polymerization reaction Methods 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- SYECJBOWSGTPLU-UHFFFAOYSA-N hexane-1,1-diamine Chemical compound CCCCCC(N)N SYECJBOWSGTPLU-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 239000004761 kevlar Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical compound OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- POPACFLNWGUDSR-UHFFFAOYSA-N methoxy(trimethyl)silane Chemical compound CO[Si](C)(C)C POPACFLNWGUDSR-UHFFFAOYSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- HNEGQIOMVPPMNR-UHFFFAOYSA-N methylfumaric acid Natural products OC(=O)C(C)=CC(O)=O HNEGQIOMVPPMNR-UHFFFAOYSA-N 0.000 description 1
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- CYCFYXLDTSNTGP-UHFFFAOYSA-L octadecanoate;tin(2+) Chemical compound [Sn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CYCFYXLDTSNTGP-UHFFFAOYSA-L 0.000 description 1
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- 239000003960 organic solvent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000009840 oxygen flask method Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
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- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
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- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
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- 229920002647 polyamide Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
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- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920001955 polyphenylene ether Polymers 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
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- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
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- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
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- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 description 1
- 229920002397 thermoplastic olefin Polymers 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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- 239000011787 zinc oxide Substances 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
Landscapes
- Adhesives Or Adhesive Processes (AREA)
Abstract
Description
本発明は、接着剤組成物に関し、さらに詳しくはポリオレフィン等の難接着性基材に適用できる塗料、接着剤等に使用できる接着剤組成物に関する。 The present invention relates to an adhesive composition, and more particularly to an adhesive composition that can be used for paints, adhesives, and the like that can be applied to difficult-to-adhere substrates such as polyolefins.
ポリオレフィンやポリオレフィン系熱可塑性エラストマー（以下、ＴＰＯと略す）は、難接着性基材として知られており、優れた接着性を示す接着剤組成物が必要とされている。これに対し、ポリオレフィンに使用される接着剤組成物として、例えば、加水分解性シリル基を有する（メタ）アクリル酸アルキルエステル共重合体と、加水分解性シリル基を有するポリオキシアルキレン重合体と、塩素化ポリオレフィン樹脂とを含むポリオレフィン用接着剤組成物が提案されている（特許文献１）。また、ＴＰＯに使用される接着剤用の硬化剤組成物として、例えば、反応性ケイ素基を有するポリオキシアルキレン系重合体と、ポリオレフィン系重合体と、粘着付与樹脂を含む組成物が提案されている（特許文献２）。 Polyolefins and polyolefin-based thermoplastic elastomers (hereinafter abbreviated as TPO) are known as difficult-to-adhere base materials, and an adhesive composition exhibiting excellent adhesiveness is required. On the other hand, as an adhesive composition used for polyolefin, for example, a (meth) acrylic acid alkyl ester copolymer having a hydrolyzable silyl group, a polyoxyalkylene polymer having a hydrolyzable silyl group, A polyolefin adhesive composition containing a chlorinated polyolefin resin has been proposed (Patent Document 1). Further, as a curing agent composition for an adhesive used in TPO, for example, a composition including a polyoxyalkylene polymer having a reactive silicon group, a polyolefin polymer, and a tackifying resin has been proposed. (Patent Document 2).
しかしながら、実用に耐えうる接着強度を得るためには、必然的にプライマー処理を行わざるを得ず、接着作業の工程数が増大し、作業性が悪いという問題がある。 However, in order to obtain an adhesive strength that can withstand practical use, the primer treatment is inevitably performed, and there is a problem that the number of steps of the bonding operation increases and the workability is poor.
そこで、本発明は、ポリオレフィン等の難接着性基材に対して、プライマー処理が不要で、実用に耐えうる良好な接着強度を得ることが可能な接着剤組成物を提供することを目的とした。 Therefore, the present invention has an object of providing an adhesive composition that can obtain a good adhesive strength that can withstand practical use without requiring a primer treatment for a difficult-to-adhere substrate such as polyolefin. .
本発明者らは、上記課題を解消すべく鋭意研究した結果、加水分解性ケイ素基を有する重合体と、分子量分布が１．５〜４．０で、融点が２０〜５０℃であるα−ポリオレフィンを塩素化してなる、塩素含有率が２０〜５０重量％である塩素化ポリオレフィンを含む樹脂組成物を用いたところ、プライマー処理なしでポリオレフィンやＴＰＯに対して優れた接着強度が得られることを見出して本発明を完成させたものである。
すなわち、本発明の接着剤組成物は、加水分解性ケイ素基を有する重合体１００重量部に対して、分子量分布が１．５〜４．０で、融点が２０〜５０℃であるα−ポリオレフィンを塩素化してなる、塩素含有率が２０〜５０重量％である塩素化ポリオレフィンを１．０〜２０．０重量部含むことを特徴とする。
As a result of diligent research to solve the above-mentioned problems, the present inventors have found that a polymer having a hydrolyzable silicon group, a molecular weight distribution of 1.5 to 4.0, and a melting point of 20 to 50 ° C. When a resin composition containing chlorinated polyolefin having a chlorine content of 20 to 50% by weight obtained by chlorinating polyolefin is used, excellent adhesion strength to polyolefin and TPO can be obtained without primer treatment. The present invention has been found and completed.
That is, the adhesive composition of the present invention is an α-polyolefin having a molecular weight distribution of 1.5 to 4.0 and a melting point of 20 to 50 ° C. with respect to 100 parts by weight of a polymer having a hydrolyzable silicon group. It is characterized by containing 1.0 to 20.0 parts by weight of chlorinated polyolefin having a chlorine content of 20 to 50% by weight.
本発明の接着剤組成物は、プライマー処理なしでポリオレフィンやＴＰＯに対して優れた接着強度を付与することが可能である。 The adhesive composition of the present invention can impart excellent adhesive strength to polyolefin and TPO without primer treatment.
以下、本発明の実施の形態について詳細に説明する。
本発明の接着剤組成物は、加水分解性ケイ素基を有する重合体１００重量部に対して、分子量分布が１．５〜４．０で、融点が２０〜５０℃であるα−ポリオレフィンを塩素化してなる、塩素含有率が２０〜５０重量％である塩素化ポリオレフィンを１．０〜２０．０重量部含むことを特徴とするものである。
Hereinafter, embodiments of the present invention will be described in detail.
The adhesive composition of the present invention is a chlorine-based α-polyolefin having a molecular weight distribution of 1.5 to 4.0 and a melting point of 20 to 50 ° C. with respect to 100 parts by weight of a polymer having a hydrolyzable silicon group. It is characterized by containing 1.0 to 20.0 parts by weight of a chlorinated polyolefin having a chlorine content of 20 to 50% by weight.
加水分解性ケイ素基を有する重合体（以下、重合体Ａという）の主鎖には、オキシアルキレン重合体又はビニル系重合体を用いる。オキシアルキレン重合体には、−ＣＨ２ＣＨ２Ｏ−、−ＣＨ２ＣＨ（ＣＨ３）Ｏ−、−ＣＨ２ＣＨ（Ｃ２Ｈ５）Ｏ−、−ＣＨ（ＣＨ３）ＣＨ２Ｏ−、−ＣＨ（Ｃ２Ｈ５）ＣＨ２Ｏ−、−ＣＨ２ＣＨ２ＣＨ２Ｏ−、及び−ＣＨ２ＣＨ２ＣＨ２ＣＨ２Ｏ−から選択された１種以上の繰り返し単位からなるものを用いることができる。好ましくは、−ＣＨ２ＣＨ（ＣＨ３）Ｏ−である。また、ビニル系重合体には、ポリエチレン、ポリプロピレン、ポリイソブチレン、ポリ（メタ）アクリレート、ポリスチレン、ポリ塩化ビニル、ポリ塩化ビニリデン、ポリブタジエン、ポリイソプレン、ポリ酢酸ビニル、ポリビニルアルコール、ポリビニルブチラール、及びこれら重合体のいずれか２種以上を成分として含む共重合体等を挙げることができる。好ましくは、ポリ（メタ）アクリレートである。 An oxyalkylene polymer or a vinyl polymer is used for the main chain of a polymer having a hydrolyzable silicon group (hereinafter referred to as polymer A). Oxyalkylene polymers include -CH2CH2O-, -CH2CH (CH3) O-, -CH2CH (C2H5) O-, -CH (CH3) CH2O-, -CH (C2H5) CH2O-, -CH2CH2CH2O-, and -CH2CH2CH2CH2O. Those consisting of one or more repeating units selected from-can be used. Preferably, it is -CH2CH (CH3) O-. Vinyl polymers include polyethylene, polypropylene, polyisobutylene, poly (meth) acrylate, polystyrene, polyvinyl chloride, polyvinylidene chloride, polybutadiene, polyisoprene, polyvinyl acetate, polyvinyl alcohol, polyvinyl butyral, and their weights. The copolymer etc. which contain any 2 or more types of a compound as a component can be mentioned. Poly (meth) acrylate is preferable.
主鎖にオキシアルキレン重合体を用いた場合、重合体Ａの分子量は、５００〜３００００、好ましくは５０００〜２００００である。ここで、重合体Ａの分子量は、原料である水酸基末端オキシアルキレン重合体の水酸基価換算分子量に基づいて算出した数平均分子量である。 When an oxyalkylene polymer is used for the main chain, the molecular weight of the polymer A is 500 to 30000, preferably 5000 to 20000. Here, the molecular weight of the polymer A is a number average molecular weight calculated based on the hydroxyl value-converted molecular weight of the hydroxyl group-terminated oxyalkylene polymer as a raw material.
また、主鎖にビニル系重合体を用いた場合、重合体Ａの数平均分子量は３０００〜５００００、好ましくは５０００〜４００００である。 Further, when a vinyl polymer is used for the main chain, the number average molecular weight of the polymer A is 3000 to 50000, preferably 5000 to 40000.
また、加水分解性ケイ素基は分子鎖末端に対する加水分解性ケイ素基の導入率が５０％以上であれば十分である。ここで、分子鎖末端に対する加水分解性ケイ素基の導入率は、末端基が水酸基である場合、加水分解性ケイ素基導入後の未反応の水酸基を水酸基価分析法を用いて算出することができる。また、末端基の種類に限定されない方法として、ＩＲ法やＮＭＲ法を用いて加水分解性ケイ素基導入後の末端基を定量することにより算出する方法を用いることもできる。 The hydrolyzable silicon group is sufficient if the introduction rate of the hydrolyzable silicon group with respect to the molecular chain terminal is 50% or more. Here, when the terminal group is a hydroxyl group, the introduction rate of the hydrolyzable silicon group with respect to the molecular chain terminal can be calculated using the hydroxyl value analysis method for the unreacted hydroxyl group after the introduction of the hydrolyzable silicon group. . Moreover, as a method not limited to the kind of terminal group, a method of calculating by quantifying the terminal group after introduction of the hydrolyzable silicon group using IR method or NMR method can also be used.
加水分解性ケイ素基は、例えば、以下の一般式（Ｉ）で表すことができる。
−ＳｉＲ３−ａＸａ （Ｉ）
ここで、Ｒは、炭素数１〜２０のアルキル基、好ましくは炭素数１〜６のアルキル基、Ｘは水酸基または炭素数１〜６のアルコキシ基、ａは１、２または３である。
The hydrolyzable silicon group can be represented by the following general formula (I), for example.
-SiR 3-a X a (I)
Here, R is an alkyl group having 1 to 20 carbon atoms, preferably an alkyl group having 1 to 6 carbon atoms, X is a hydroxyl group or an alkoxy group having 1 to 6 carbon atoms, and a is 1, 2 or 3.
例えば、加水分解性ケイ素基には、アルキルジアルコキシシリル基やトリアルコキシシリル基を用いることができる。アルキルジアルコキシシリル基は、アルキル基が炭素数１から６のアルキル基が好ましく、アルコキシ基が炭素数１から６のアルコキシ基、すなわち、メトキシ基、エトキシ基、プロポキシ基、ブトキシ基、ペンチルオキシ基又はｎ−ヘキシルオキシ基が好ましく、より好ましくはメチルジメトキシシリル基又はメチルジエトキシシリル基、さらに好ましくはメチルジメトキシシリル基である。また、トリアルコキシシリル基は、アルコキシ基が炭素数１から６のアルコキシ基、すなわち、メトキシ基、エトキシ基、プロポキシ基、ブトキシ基、ペンチルオキシ基、ｎ−ヘキシルオキシ基が好ましく、より好ましくはトリメトキシシリル基である。 For example, an alkyl dialkoxysilyl group or a trialkoxysilyl group can be used for the hydrolyzable silicon group. The alkyl dialkoxysilyl group is preferably an alkyl group having 1 to 6 carbon atoms, and an alkoxy group having 1 to 6 carbon atoms, that is, a methoxy group, an ethoxy group, a propoxy group, a butoxy group, or a pentyloxy group. Alternatively, an n-hexyloxy group is preferable, a methyldimethoxysilyl group or a methyldiethoxysilyl group is more preferable, and a methyldimethoxysilyl group is still more preferable. The trialkoxysilyl group is preferably an alkoxy group having 1 to 6 carbon atoms, that is, a methoxy group, an ethoxy group, a propoxy group, a butoxy group, a pentyloxy group, or an n-hexyloxy group, more preferably a trialkoxy group. It is a methoxysilyl group.
オキシアルキレン重合体に加水分解性ケイ素基を導入する方法としては、２官能の開始剤の存在下、環状エーテルを開環重合させてオキシアルキレンジオールを製造し、このジオールの水酸基に加水分解性ケイ素基を導入する方法等の公知の方法を用いることができる。また、ビニル系重合体に加水分解性ケイ素基を導入する方法としては、ビニル系モノマーと、加水分解性ケイ素基含有モノマーとを共重合する方法を用いることができる。加水分解性ケイ素基の導入率を変化させる方法としては、オキシアルキレン重合体の場合、ジオールの水酸基に対する加水分解性ケイ素基のモル数を変化させることに行うことができる。また、ビニル系重合体の場合、共重合させる加水分解性ケイ素基含有モノマーの配合比を変化させることにより加水分解性ケイ素基の導入率を変化させることができる。 As a method for introducing a hydrolyzable silicon group into an oxyalkylene polymer, an oxyalkylene diol is produced by ring-opening polymerization of a cyclic ether in the presence of a bifunctional initiator, and hydrolyzable silicon is added to the hydroxyl group of the diol. A known method such as a method for introducing a group can be used. In addition, as a method for introducing a hydrolyzable silicon group into a vinyl polymer, a method of copolymerizing a vinyl monomer and a hydrolyzable silicon group-containing monomer can be used. As a method of changing the introduction rate of the hydrolyzable silicon group, in the case of an oxyalkylene polymer, it can be performed by changing the number of moles of the hydrolyzable silicon group with respect to the hydroxyl group of the diol. In the case of vinyl polymers, the introduction rate of hydrolyzable silicon groups can be changed by changing the blending ratio of hydrolyzable silicon group-containing monomers to be copolymerized.
また、重合体Ａとして本発明に使用可能な重合体は、変性シリコーン樹脂として上市されている、例えば以下のものを挙げることができるが、これらに限定されるものではない。
・株式会社カネカ製 ＭＳポリマーＳ２０３（メチルジメトキシシリル基を有するオキシアルキレン重合体）
・株式会社カネカ製 サイリルＭＡ４４０（メチルジメトキシシリル基を有するオキシアルキレン重合体とアルコキシシリル基を有するアクリル重合体の混合物）
・株式会社カネカ製 サイリルＳＸ５８０（トリメトキシシリル基を有するオキシアルキレン重合体）
・旭硝子株式会社製 ＥＸＣＥＳＴＡＲ Ｓ２４２０（メチルジメトキシシリル基を有するオキシアルキレン重合体）
・ワッカーケミー社製 ＳＴＰ Ｅ−３０（トリメトキシシリル基を有するオキシアルキレン重合体）
Moreover, the polymer which can be used for this invention as the polymer A can list the following, for example as a modified silicone resin, However, It is not limited to these.
-Kaneka Corporation MS polymer S203 (oxyalkylene polymer having a methyldimethoxysilyl group)
・ Kaneka Co., Ltd. Silyl MA440 (mixture of oxyalkylene polymer having methyldimethoxysilyl group and acrylic polymer having alkoxysilyl group)
・ Sailyl SX580 (oxyalkylene polymer having a trimethoxysilyl group) manufactured by Kaneka Corporation
-EXCESTAR S2420 (oxyalkylene polymer having a methyldimethoxysilyl group) manufactured by Asahi Glass Co., Ltd.
-STP E-30 (oxyalkylene polymer having a trimethoxysilyl group) manufactured by Wacker Chemie
本発明で用いる塩素化ポリオレフィンは、α−ポリオレフィンを塩素化したものである。α−ポリオレフィンとしては、ポリエチレン、ポリプロピレン、ポリ（１−ブテン）等を挙げることができるが、ポリプロピレンが好ましい。また、ポリプロピレンとしては、プロピレンの単独重合体や、プロピレンと他のα−オレフィンとの共重合体を用いることができる。共重合体に用いるα−オレフィンとしては、エチレン、１−ブテン、１−ペンテン、１−ヘキセン、１−ヘプテン、１−オクテン等を挙げることができるが、エチレンが好ましい。なお、ポリオレフィンに対する接着性の観点から、この共重合体中のプロピレン成分の含有量は５０モル％以上であることが好ましい。 The chlorinated polyolefin used in the present invention is a chlorinated α-polyolefin. Examples of the α-polyolefin include polyethylene, polypropylene, poly (1-butene) and the like, and polypropylene is preferable. Moreover, as a polypropylene, the homopolymer of propylene and the copolymer of propylene and another alpha olefin can be used. Examples of the α-olefin used for the copolymer include ethylene, 1-butene, 1-pentene, 1-hexene, 1-heptene, 1-octene and the like, and ethylene is preferable. From the viewpoint of adhesion to polyolefin, the content of the propylene component in the copolymer is preferably 50 mol% or more.
また、本発明で用いる塩素化ポリオレフィンには、酸変性塩素化ポリオレフィンも含まれる。酸変性塩素化ポリオレフィンは、α，β−不飽和カルボン酸および／またはその誘導体をポリオレフィンに導入した酸変性ポリオレフィンに塩素を導入したものである。α，β−不飽和カルボン酸としては、マレイン酸、無水マレイン酸、フマル酸、シトラコン酸、無水シトラコン酸、メサコン酸、イタコン酸、無水イタコン酸、（メタ）アクリル酸、（メタ）アクリル酸エステル等を挙げることができるが、無水マレイン酸が好ましい。α，β−不飽和カルボン酸は、例えばグラフト重合により導入することができ、その場合、導入率は１〜２０重量％、好ましくは１〜１０重量％である。 The chlorinated polyolefin used in the present invention also includes acid-modified chlorinated polyolefin. The acid-modified chlorinated polyolefin is obtained by introducing chlorine into an acid-modified polyolefin obtained by introducing an α, β-unsaturated carboxylic acid and / or a derivative thereof into the polyolefin. As α, β-unsaturated carboxylic acid, maleic acid, maleic anhydride, fumaric acid, citraconic acid, citraconic anhydride, mesaconic acid, itaconic acid, itaconic anhydride, (meth) acrylic acid, (meth) acrylic acid ester Maleic anhydride is preferable. The α, β-unsaturated carboxylic acid can be introduced by, for example, graft polymerization. In this case, the introduction rate is 1 to 20% by weight, preferably 1 to 10% by weight.
本発明で用いる塩素化ポリオレフィンの塩素含有率は、２０〜５０重量％、好ましくは２３〜４０重量％、より好ましくは２７〜３３重量％である。２０重量％より小さいと有機溶媒への溶解性が十分ではなく、また５０重量％より大きいと基材への接着性が低下するからである。塩素含有率は、ＪＩＳ−Ｋ７２２９に準じて酸素フラスコ燃焼法で測定することができる。すなわち、塩素化ポリオレフィンを酸素雰囲気で燃焼させ、発生した気体塩素を水で吸収し、滴定により定量することができる。 The chlorine content of the chlorinated polyolefin used in the present invention is 20 to 50% by weight, preferably 23 to 40% by weight, more preferably 27 to 33% by weight. This is because if it is less than 20% by weight, the solubility in an organic solvent is not sufficient, and if it is more than 50% by weight, the adhesion to the substrate is lowered. The chlorine content can be measured by an oxygen flask combustion method according to JIS-K7229. That is, chlorinated polyolefin can be burned in an oxygen atmosphere, and gaseous chlorine generated can be absorbed with water and quantified by titration.
本発明に用いる塩素化ポリオレフィンは、原料に、分子量分布が１．５〜４．０、好ましくは１．５〜３．０、より好ましくは２．０〜３．０であるα−ポリオレフィンを用いて塩素化したものである。ここで、分子量分布とは、ゲルパーミエーション（ＧＰＣ）法で測定されるＭｗ／Ｍｎの値である。 The chlorinated polyolefin used in the present invention uses an α-polyolefin having a molecular weight distribution of 1.5 to 4.0, preferably 1.5 to 3.0, more preferably 2.0 to 3.0 as a raw material. Chlorinated. Here, the molecular weight distribution is a value of Mw / Mn measured by a gel permeation (GPC) method.
また、本発明に用いる塩素化ポリオレフィンの原料のα−ポリオレフィンのＴｍ（融点）は、２０〜５０℃、好ましくは２０〜４０℃、より好ましくは２０〜３０℃である。ここで、Ｔｍは示差走査熱量測定（ＤＳＣ）法により測定することができる。 Moreover, Tm (melting | fusing point) of (alpha) -polyolefin which is a raw material of chlorinated polyolefin used for this invention is 20-50 degreeC, Preferably it is 20-40 degreeC, More preferably, it is 20-30 degreeC. Here, Tm can be measured by a differential scanning calorimetry (DSC) method.
また、塩素化ポリオレフィンとして本発明に使用可能なものとして、例えば以下の上市されている塩素化ポリオレフィンを挙げることができるが、これに限定されるものではない。
・東洋紡株式会社製 ハードレンＤＸ−５３０Ｐ（塩素含有率３０重量％、塩素化ポリプロピレン、原料ポリプロピレンのＭｗ／Ｍｎ＝２．５、Ｔｍ（融点）＝３０℃）
Examples of chlorinated polyolefins that can be used in the present invention include the following commercially available chlorinated polyolefins, but are not limited thereto.
-Toyobo Co., Ltd. HARDREN DX-530P (chlorine content 30% by weight, chlorinated polypropylene, raw material polypropylene Mw / Mn = 2.5, Tm (melting point) = 30 ° C.)
本発明の組成物は、重合体Ａ １００重量部に対して、塩素化ポリオレフィンの含有量が、１．０〜２０．０重量部、好ましくは１．０〜１５．０重量部、より好ましくは１．０〜１０．０重量部である。１．０重量部より少ないと、ポリオレフィンに対する接着性が低下し、２０．０重量部より多いと塩素化ポリオレフィンが重合体Ａと分離し易くなるからである。 The composition of the present invention has a chlorinated polyolefin content of 1.0 to 20.0 parts by weight, preferably 1.0 to 15.0 parts by weight, more preferably 100 parts by weight of the polymer A. 1.0 to 10.0 parts by weight. When the amount is less than 1.0 part by weight, the adhesion to polyolefin is lowered, and when the amount is more than 20.0 parts by weight, the chlorinated polyolefin is easily separated from the polymer A.
本発明の組成物には、溶剤、硬化触媒、充填剤、粘着付与剤、可塑剤、脱水剤等の公知の添加剤を添加することができる。 Known additives such as a solvent, a curing catalyst, a filler, a tackifier, a plasticizer, and a dehydrating agent can be added to the composition of the present invention.
溶剤としては、イソパラフィン系溶剤を用いることができる。イソパラフィン系溶剤としては、例えば上市されている以下のものを用いることができるが、それに限定されるものではない。また、組成物中の溶剤の濃度は、１．０〜２０．０重量％、好ましくは１．０〜１０．０重量％である。
・安藤パラケミー株式会社製 アイソパーＧ
・安藤パラケミー株式会社製 アイソパーＨ
・安藤パラケミー株式会社製 アイソパーＭ
As the solvent, an isoparaffin-based solvent can be used. As the isoparaffinic solvent, for example, the following commercially available ones can be used, but are not limited thereto. Moreover, the density | concentration of the solvent in a composition is 1.0-20.0 weight%, Preferably it is 1.0-10.0 weight%.
・ Isopar G manufactured by Ando Parachemy Co., Ltd.
・ Isopar H manufactured by Ando Parachemy Co., Ltd.
・ Isopar M manufactured by Ando Parachemy Co., Ltd.
また、硬化反応を促進させるために硬化触媒を用いることもできる。例えば、アルキルチタン酸塩、有機ケイ素チタン酸塩、ビスマストリス−２−エチルヘキサノエート等の金属塩、リン酸、ｐ−トルエンスルホン酸、フタル酸等の酸性化合物、ブチルアミン、ヘキシルアミン、オクチルアミン、デシルアミン、ラウリルアミン等の脂肪族モノアミン、エチレンジアミン、ヘキサンジアミン等の脂肪族ジアミン、ジエチレントリアミン、トリエチレンテトラミン、テトラエチレンペンタミン等の脂肪族ポリアミン類、ピペリジン、ピペラジン等の複素環式アミン類、メタフェニレンジアミン等の芳香族アミン類、エタノールアミン類、トリエチルアミン、エポキシ樹脂の硬化剤として用いられる各種変性アミン等のアミン化合物を挙げることができる。また、ジオクチル酸スズ、ジナフテン酸スズ、ジステアリン酸スズ等の有機アルキルスズ塩と上記アミン類の混合物を挙げることもできる。また、有機アルキルスズオキシドとエチルシリケート、マレイン酸ジメチル、マレイン酸ジエチル、マレイン酸ジオクチル、フタル酸ジメチル、フタル酸ジエチル、フタル酸ジオクチル等のエステル化合物との反応生成物を挙げることもできる。またキレートスズ化合物とアルコキシシランとの反応生成物を挙げることもできる。 A curing catalyst can also be used to accelerate the curing reaction. For example, metal salts such as alkyl titanates, organosilicon titanates, bismuth tris-2-ethylhexanoate, acidic compounds such as phosphoric acid, p-toluenesulfonic acid, phthalic acid, butylamine, hexylamine, octylamine , Aliphatic monoamines such as decylamine and laurylamine, aliphatic diamines such as ethylenediamine and hexanediamine, aliphatic polyamines such as diethylenetriamine, triethylenetetramine and tetraethylenepentamine, heterocyclic amines such as piperidine and piperazine, meta Examples include amine compounds such as aromatic amines such as phenylenediamine, ethanolamines, triethylamine, and various modified amines used as curing agents for epoxy resins. Moreover, the mixture of organic alkyl tin salts, such as tin dioctylate, tin dinaphthenate, and tin distearate, and the said amines can also be mentioned. Moreover, the reaction product of ester compounds, such as an organic alkyl tin oxide, ethyl silicate, dimethyl maleate, diethyl maleate, dioctyl maleate, dimethyl phthalate, diethyl phthalate, dioctyl phthalate, can also be mentioned. Moreover, the reaction product of a chelate tin compound and alkoxysilane can also be mentioned.
また、充填剤としては、充填剤としては、公知の充填剤を使用することができる。例えば、表面を脂肪酸または樹脂酸系有機物で表面処理した炭酸カルシウム、さらにこれを微粉末化した平均粒径１μｍ以下の膠質炭酸カルシウム、沈降法により製造した平均粒径１〜３μｍの軽質炭酸カルシウム、平均粒径１〜２０μｍの重質炭酸カルシウム等の炭酸カルシウム、フュームドシリカ、沈降性シリカ、無水ケイ酸、含水ケイ酸、およびカーボンブラック、炭酸マグネシウム、ケイソウ土、焼成クレー、クレー、タルク、酸化チタン、ベントナイト、有機ベントナイト、酸化第二鉄、酸化亜鉛、活性亜鉛華、シラスバルーン、木粉、パルプ、木綿チップ、マイカ、くるみ穀粉、もみ穀粉、グラファイト、アルミニウム微粉末、フリント粉末等の粉体状充填剤、ガラス繊維、ガラスフィラメント、炭素繊維、ケブラー繊維、ポリエチレンファイバー等の繊維状充填剤等を挙げることができる。これらの充填剤は単独で用いてもよく、２種以上併用してもよい。 Moreover, as a filler, a well-known filler can be used as a filler. For example, calcium carbonate whose surface is treated with a fatty acid or a resin acid organic substance, fine calcium carbonate powder having an average particle diameter of 1 μm or less, light calcium carbonate having an average particle diameter of 1 to 3 μm manufactured by a precipitation method, Calcium carbonate such as heavy calcium carbonate with an average particle size of 1 to 20 μm, fumed silica, precipitated silica, anhydrous silicic acid, hydrous silicic acid, and carbon black, magnesium carbonate, diatomaceous earth, calcined clay, clay, talc, oxidation Titanium, bentonite, organic bentonite, ferric oxide, zinc oxide, activated zinc white, shirasu balloon, wood flour, pulp, cotton chips, mica, walnut flour, rice flour, graphite, aluminum fine powder, flint powder, etc. Filler, glass fiber, glass filament, carbon fiber, Kevlar fiber, polyester Mention may be made of a fibrous filler such as Ren fiber. These fillers may be used alone or in combination of two or more.
また、粘着付与剤としては、フェノール樹脂、テルペン樹脂、石油系樹脂、ロジン系樹脂等の公地の粘着付与剤を用いることができる。好ましくは、水素基含有水素化石油樹脂である。 Moreover, as a tackifier, public tackifiers, such as a phenol resin, a terpene resin, a petroleum resin, and a rosin resin, can be used. Preferably, it is a hydrogen group-containing hydrogenated petroleum resin.
また、可塑剤を用いて硬度調整を行うことができ、例えば、フタル酸ジオクチル、フタル酸ジブチル、フタル酸ブチルベンジル等のフタル酸アルキルエステル類；アジピン酸ジオクチル、コハク酸ジイソデシル、セバシン酸ジブチル、オレイン酸ブチル等の脂肪族カルボン酸アルキルエステル類；ペンタエリスリトールエステル等；リン酸トリオクチル、リン酸トリクレジル等のリン酸エステル類；エポキシ化大豆油、エポキシステアリン酸ベンジル等のエポキシ可塑剤；ポリプロピレングリコール；ポリエチレングリコール；塩素化パラフィン；等を挙げることができる。これらの可塑剤を単独で用いてもよく、２種以上併用してもよい。 Further, the hardness can be adjusted using a plasticizer, for example, phthalic acid alkyl esters such as dioctyl phthalate, dibutyl phthalate, butyl benzyl phthalate; dioctyl adipate, diisodecyl succinate, dibutyl sebacate, olein Aliphatic carboxylic acid alkyl esters such as butyl acid; pentaerythritol esters and the like; phosphoric acid esters such as trioctyl phosphate and tricresyl phosphate; epoxy plasticizers such as epoxidized soybean oil and benzyl epoxy stearate; polypropylene glycol; polyethylene Glycol; chlorinated paraffin; and the like. These plasticizers may be used alone or in combination of two or more.
また、脱水剤として、硬化物の物性や硬化性及び貯蔵安定性を調節する目的で加水分解性ケイ素化合物を任意に添加できる。具体例としては、テトラメチルシリケート、ビニルトリメトキシシラン、メチルトリメトキシシラン、ジメチルジメトキシシラン、トリメチルメトキシシランなどやこれらのメトキシ基がエトキシ基に置換された化合物などを挙げることができるが、これらに限定されない。 Further, as a dehydrating agent, a hydrolyzable silicon compound can be optionally added for the purpose of adjusting the physical properties, curability and storage stability of the cured product. Specific examples include tetramethyl silicate, vinyltrimethoxysilane, methyltrimethoxysilane, dimethyldimethoxysilane, trimethylmethoxysilane, and the like, and compounds in which these methoxy groups are substituted with ethoxy groups. It is not limited.
なお、本明細書で用いるポリオレフィン等の難接着性基材には、ポリエチレン、ポリプロピレン、エチレンプロピレン共重合体、エチレンプロピレンジエン共重合体等のポリオレフィン樹脂；オレフィン系熱可塑性エラストマー；ポリアセタール、ポリアミド、ポリカーボネイト、変成ポリフェニレンエーテル、ポリブチレンテレフタレート等のエンジニアリングプラスチックが含まれる。 In addition, the difficult-to-adhere base materials such as polyolefin used in the present specification include polyolefin resins such as polyethylene, polypropylene, ethylene propylene copolymer and ethylene propylene diene copolymer; olefin thermoplastic elastomers; polyacetal, polyamide, polycarbonate Engineering plastics such as modified polyphenylene ether and polybutylene terephthalate.
以下、実施例を用いて本発明を説明するが、本発明は以下の実施例に限定されるものではない。 EXAMPLES Hereinafter, although this invention is demonstrated using an Example, this invention is not limited to a following example.
実験例１
アイソパーＧ（安藤パラケミー社製：イソパラフィン系炭化水素）６ｇにハードレンＤＸ−５３０Ｐ（東洋紡社製：塩素化ポリプロピレン、原料ポリプロピレンのＭｗ／Ｍｎ＝２．５、Ｔｍ＝３０℃）３ｇを溶解させ、サイリルＳＡＸ５８０（カネカ社製：変成シリコーン樹脂）を１００ｇ、エクセノール３０２０（旭硝子社製：ポリエチレングリコール）を８０ｇ、ハクエンカＣＣＲ（白石工業社製：炭酸カルシウム）を１５０ｇ、それぞれ自公転式攪拌機に添加し、撹拌することによって混練した。その混合物にＺ−６３００（東レ・ダウコーニング社製：ビニルトリメトキシシラン）を４ｇ、Ｚ−６０９４（東レ・ダウコーニング社製：３−（２−（アミノエチル）アミノプロピルトリメトキシシラン）を５ｇ、ネオスタンＳ−１（日東化成社製：アルキルスズ塩とシリケートの反応物）を０．６ｇそれぞれ添加し組成物を調製した。得られた組成物の組成を表１に示す。
Experimental example 1
Hardylene DX-530P (manufactured by Toyobo Co., Ltd .: chlorinated polypropylene, Mw / Mn of raw material polypropylene, Tm = 30 ° C.) 3 g was dissolved in 6 g of Isopar G (produced by Ando Parachemy Co., Ltd .: isoparaffinic hydrocarbon). 100 g of SAX580 (manufactured by Kaneka: modified silicone resin), 80 g of Exenol 3020 (manufactured by Asahi Glass Co., Ltd .: polyethylene glycol), and 150 g of Hakuenka CCR (manufactured by Shiraishi Kogyo Co., Ltd .: calcium carbonate) were added to the revolving stirrer and stirred. Kneaded. 4 g of Z-6300 (Toray Dow Corning: vinyltrimethoxysilane) and 5 g of Z-6094 (Toray Dow Corning: 3- (2- (aminoethyl) aminopropyltrimethoxysilane) were added to the mixture. A composition was prepared by adding 0.6 g of Neostan S-1 (manufactured by Nitto Kasei Co., Ltd .: reaction product of alkyl tin salt and silicate), and the composition of the obtained composition is shown in Table 1.
実験例２
アイソパーＧ（安藤パラケミー社製：イソパラフィン系炭化水素）６ｇにハードレンＦ−６Ｐ（東洋紡社製：酸変性塩素化ポリプロピレン、原料ポリプロピレンのＭｗ／Ｍｎ＝２．６、Ｔｍ＝７０℃）３ｇを溶解させ、サイリルＳＡＸ５８０（カネカ社製：変成シリコーン樹脂）を１００ｇ、エクセノール３０２０（旭硝子社製：ポリエチレングリコール）を８０ｇ、ハクエンカＣＣＲ（白石工業社製：炭酸カルシウム）を１５０ｇ、それぞれ自公転式攪拌機に添加し、撹拌することによって混練した。その混合物にＺ−６３００（東レ・ダウコーニング社製：ビニルトリメトキシシラン）を４ｇ、Ｚ−６０９４（東レ・ダウコーニング社製：３−（２−（アミノエチル）アミノプロピルトリメトキシシラン）を５ｇ、ネオスタンＳ−１（日東化成社製：アルキルスズ塩とシリケートの反応物）を０．６ｇそれぞれ添加し組成物を調製した。得られた組成物の組成を表１に示す。
Experimental example 2
3 g of Hardren F-6P (Toyobo Co., Ltd .: acid-modified chlorinated polypropylene, Mw / Mn of raw material polypropylene, Tm = 70 ° C.) was dissolved in 6 g of Isopar G (manufactured by Ando Parachemy). 100 g of Silyl SAX580 (manufactured by Kaneka Corporation: modified silicone resin), 80 g of Exenol 3020 (manufactured by Asahi Glass Company: polyethylene glycol), and 150 g of Hakuenka CCR (manufactured by Shiraishi Kogyo Co., Ltd .: calcium carbonate) were added to the revolving stirrer. The mixture was kneaded by stirring. 4 g of Z-6300 (Toray Dow Corning: vinyltrimethoxysilane) and 5 g of Z-6094 (Toray Dow Corning: 3- (2- (aminoethyl) aminopropyltrimethoxysilane) were added to the mixture. A composition was prepared by adding 0.6 g of Neostan S-1 (manufactured by Nitto Kasei Co., Ltd .: reaction product of alkyl tin salt and silicate), and the composition of the obtained composition is shown in Table 1.
実験例３
アイソパーＧ（安藤パラケミー社製：イソパラフィン系炭化水素）６ｇにハードレン１４−ＬＷＰ（東洋紡社製：塩素化ポリプロピレン、原料ポリプロピレンのＭｗ／Ｍｎ＝２．６，Ｔｍ＝８０℃）３ｇを溶解させ、サイリルＳＡＸ５８０（カネカ社製：変成シリコーン樹脂）を１００ｇ、エクセノール３０２０（旭硝子社製：ポリエチレングリコール）を８０ｇ、ハクエンカＣＣＲ（白石工業社製：炭酸カルシウム）を１５０ｇ、それぞれ自公転式攪拌機に添加し、撹拌することによって混練した。その混合物にＺ−６３００（東レ・ダウコーニング社製：ビニルトリメトキシシラン）を４ｇ、Ｚ−６０９４（東レ・ダウコーニング社製：３−（２−（アミノエチル）アミノプロピルトリメトキシシラン）を５ｇ、ネオスタンＳ−１（日東化成社製：アルキルスズ塩とシリケートの反応物）を０．６ｇそれぞれ添加し組成物を調製した。得られた組成物の組成を表１に示す。
Experimental example 3
Hardylene 14-LWP (manufactured by Toyobo Co., Ltd .: chlorinated polypropylene, Mw / Mn of raw material polypropylene: Tm = 80 ° C.) 3 g was dissolved in 6 g of Isopar G (produced by Ando Parachemy Co., Ltd .: isoparaffinic hydrocarbon). 100 g of SAX580 (manufactured by Kaneka: modified silicone resin), 80 g of Exenol 3020 (manufactured by Asahi Glass Co., Ltd .: polyethylene glycol), and 150 g of Hakuenka CCR (manufactured by Shiraishi Kogyo Co., Ltd .: calcium carbonate) were added to the revolving stirrer and stirred. Kneaded. 4 g of Z-6300 (Toray Dow Corning: vinyltrimethoxysilane) and 5 g of Z-6094 (Toray Dow Corning: 3- (2- (aminoethyl) aminopropyltrimethoxysilane) were added to the mixture. A composition was prepared by adding 0.6 g of Neostan S-1 (manufactured by Nitto Kasei Co., Ltd .: reaction product of alkyl tin salt and silicate), and the composition of the obtained composition is shown in Table 1.
実験例４
アイソパーＧ（安藤パラケミー社製：イソパラフィン系炭化水素）６ｇにハードレンＣＹ−９１２４Ｐ（東洋紡社製：酸変性塩素化ポリプロピレン、原料ポリプロピレンのＭｗ／Ｍｎ＝２．７，Ｔｍ＝８０℃）３ｇを溶解させ、サイリルＳＡＸ５８０（カネカ社製：変成シリコーン樹脂）を１００ｇ、エクセノール３０２０（旭硝子社製：ポリエチレングリコール）を８０ｇ、ハクエンカＣＣＲ（白石工業社製：炭酸カルシウム）を１５０ｇ、それぞれ自公転式攪拌機に添加し、撹拌することによって混練した。その混合物にＺ−６３００（東レ・ダウコーニング社製：ビニルトリメトキシシラン）を４ｇ、Ｚ−６０９４（東レ・ダウコーニング社製：３−（２−（アミノエチル）アミノプロピルトリメトキシシラン）を５ｇ、Ｓ−１（日東化成社製：アルキルスズ塩とシリケートの反応物）を０．６ｇそれぞれ添加し組成物を調製した。得られた組成物の組成を表１に示す。
Experimental Example 4
3 g of HARDREN CY-9124P (manufactured by Toyobo Co., Ltd .: acid-modified chlorinated polypropylene, raw material polypropylene Mw / Mn = 2.7, Tm = 80 ° C.) is dissolved in 6 g of ISOPAR G (manufactured by Ando Parachemie: isoparaffinic hydrocarbon). 100 g of Silyl SAX580 (manufactured by Kaneka Corporation: modified silicone resin), 80 g of Exenol 3020 (manufactured by Asahi Glass Company: polyethylene glycol), and 150 g of Hakuenka CCR (manufactured by Shiraishi Kogyo Co., Ltd .: calcium carbonate) were added to the revolving stirrer. The mixture was kneaded by stirring. 4 g of Z-6300 (Toray Dow Corning: vinyltrimethoxysilane) and 5 g of Z-6094 (Toray Dow Corning: 3- (2- (aminoethyl) aminopropyltrimethoxysilane) were added to the mixture. , S-1 (manufactured by Nitto Kasei Co., Ltd .: reaction product of alkyl tin salt and silicate) was added to prepare 0.6 g of each composition, and the composition of the obtained composition is shown in Table 1.
実験例５
アイソパーＧ（安藤パラケミー社製：イソパラフィン系炭化水素）６ｇにハードレンＤＸ−５３０Ｐ（東洋紡社製：塩素化ポリプロピレン、原料ポリプロピレンのＭｗ／Ｍｎ＝２．５、Ｔｍ＝３０℃）を３ｇ、ＫＲ−１８４０（荒川化学工業社製：水素基含有水素化石油樹脂）を６ｇ溶解させ、サイリルＳＡＸ５８０（カネカ社製：変成シリコーン樹脂）を１００ｇ、エクセノール３０２０（旭硝子社製：ポリエチレングリコール）を８０ｇ、ハクエンカＣＣＲ（白石工業社製：炭酸カルシウム）を１５０ｇ、それぞれ自公転式攪拌機に添加し、撹拌することによって混練した。その混合物にＺ−６３００（東レ・ダウコーニング社製：ビニルトリメトキシシラン）を４ｇ、Ｚ−６０９４（東レ・ダウコーニング社製：３−（２−（アミノエチル）アミノプロピルトリメトキシシラン）を５ｇ、ネオスタンＳ−１（日東化成社製：アルキルスズ塩とシリケートの反応物）を０．６ｇそれぞれ添加し組成物を調製した。得られた組成物の組成を表１に示す。
Experimental Example 5
3 g of KR-1840, 6 g of Isopar G (manufactured by Ando Parachemy: isoparaffinic hydrocarbon) and 3 g of Hardren DX-530P (manufactured by Toyobo: chlorinated polypropylene, raw material Mw / Mn = 2.5, Tm = 30 ° C.) 6 g of Arakawa Chemical Industries, Ltd. (hydrogen group-containing hydrogenated petroleum resin) are dissolved, 100 g of silyl SAX580 (manufactured by Kaneka Corporation: modified silicone resin), 80 g of Exenol 3020 (manufactured by Asahi Glass Co., Ltd .: polyethylene glycol), 150 g of Shiraishi Kogyo Co., Ltd .: calcium carbonate) was added to each of the self-revolving stirrers and kneaded by stirring. 4 g of Z-6300 (Toray Dow Corning: vinyltrimethoxysilane) and 5 g of Z-6094 (Toray Dow Corning: 3- (2- (aminoethyl) aminopropyltrimethoxysilane) were added to the mixture. A composition was prepared by adding 0.6 g of Neostan S-1 (manufactured by Nitto Kasei Co., Ltd .: reaction product of alkyl tin salt and silicate), and the composition of the obtained composition is shown in Table 1.
実験例６
アイソパーＧ（安藤パラケミー社製：イソパラフィン系炭化水素）６ｇにハードレンＣＹ−９１２４Ｐ（東洋紡社製：酸変性塩素化ポリプロピレン、原料ポリプロピレンのＭｗ／Ｍｎ＝２．７、Ｔｍ＝８０℃）を３ｇ、ＫＲ−１８４０（荒川化学工業社製：水素基含有水素化石油樹脂)を６ｇ溶解させ、サイリルＳＡＸ５８０（カネカ社製：変成シリコーン樹脂）を１００ｇ、エクセノール３０２０（旭硝子社製：ポリエチレングリコール）を８０ｇ、ハクエンカＣＣＲ（白石工業社製：炭酸カルシウム）を１５０ｇ、それぞれ自公転式攪拌機に添加し、撹拌することによって混練した。その混合物にＺ−６３００（東レ・ダウコーニング社製：ビニルトリメトキシシラン）を４ｇ、Ｚ−６０９４（東レ・ダウコーニング社製：３−（２−（アミノエチル）アミノプロピルトリメトキシシラン）を５ｇ、ネオスタンＳ−１（日東化成社製：アルキルスズ塩とシリケートの反応物）を０．６ｇそれぞれ添加し組成物を調製した。得られた組成物の組成を表１に示す。
Experimental Example 6
3 g of Hardren CY-9124P (Toyobo Co., Ltd .: acid-modified chlorinated polypropylene, raw material Mw / Mn = 2.7, Tm = 80 ° C.) to 6 g of Isopar G (manufactured by Ando Parachemy): KR -1840 (Arakawa Chemical Industries, Ltd .: hydrogenated hydrogenated petroleum resin) is dissolved, Silyl SAX580 (Kaneka: modified silicone resin) is 100 g, Exenol 3020 (Asahi Glass: polyethylene glycol) is 80 g, Hakuenka 150 g of CCR (manufactured by Shiraishi Kogyo Co., Ltd .: calcium carbonate) was added to each of the self-revolving stirrers and kneaded by stirring. 4 g of Z-6300 (Toray Dow Corning: vinyltrimethoxysilane) and 5 g of Z-6094 (Toray Dow Corning: 3- (2- (aminoethyl) aminopropyltrimethoxysilane) were added to the mixture. A composition was prepared by adding 0.6 g of Neostan S-1 (manufactured by Nitto Kasei Co., Ltd .: reaction product of alkyl tin salt and silicate), and the composition of the obtained composition is shown in Table 1.
（せん断試験）
２５×５０ｍｍのポリプロピレン板(エンジニアリングテストサービス品)に組成物を塗布面積２５×１２ｍｍで塗布し、０．１ｍｍの厚みでポリプロピレン板同士を接着し、２３℃、５０％ＲＨ条件下で７日間養生して試験用片を作製した。せん断試験は、ＪＩＳ Ｋ６８５０に準じ、引張試験機（東洋精機社製型式ストログラフＶＥ５Ｄ）を用いて行い、接着せん断強度（Ｎ／ｍｍ２）を測定した。また、破断後の試験片の表面状態は目視で観察した。表面状態は、組成物自身が破壊した場合、ポリプロピレン板に接着しているとみなして評価を○とし、組成物がポリプロピレン板から界面剥離する場合はポリプロピレン板と接着していないとみなし、評価を×とした。結果を表１に示す。
(Shear test)
The composition is applied to a 25 × 50 mm polypropylene plate (engineering test service product) with an application area of 25 × 12 mm, the polypropylene plates are bonded to each other with a thickness of 0.1 mm, and cured for 7 days under conditions of 23 ° C. and 50% RH. Thus, a test piece was produced. The shear test was performed according to JIS K6850 using a tensile tester (model strograph VE5D manufactured by Toyo Seiki Co., Ltd.), and the adhesive shear strength (N / mm 2 ) was measured. Moreover, the surface state of the test piece after the fracture was visually observed. When the composition itself is destroyed, the surface condition is considered as being adhered to the polypropylene plate, and the evaluation is ○, and when the composition peels off from the polypropylene plate, the surface state is regarded as not being adhered to the polypropylene plate and evaluated. X. The results are shown in Table 1.
（剥離試験）
２５×１００ｍｍの東洋紡社製のオレフィン系熱可塑性エラストマー（ＴＰＯ）シートに組成物を塗布面積２５×９０ｍｍで塗布し、０．１ｍｍの厚みでＴＰＯシート同士を接着し、２３℃、５０％ＲＨ条件下で７日間養生した。１８０度剥離試験は、ＪＩＳ Ｋ６８５４に準じ、引張試験機（東洋精機社製型式ストログラフＶＥ５Ｄ）を用いて行い、剥離接着強度（Ｎ／ｍｍ）を測定した。また、破断後の試験片の表面状態は目視で観察した。表面状態は、組成物自身が破壊した場合、ポリプロピレン板に接着しているとみなして評価を○とし、組成物がポリプロピレン板から界面剥離する場合はポリプロピレン板と接着していないとみなし、評価を×とした。結果を表１に示す。
(Peel test)
The composition is applied to an olefinic thermoplastic elastomer (TPO) sheet manufactured by Toyobo Co., Ltd. of 25 × 100 mm with a coating area of 25 × 90 mm, and the TPO sheets are bonded to each other with a thickness of 0.1 mm, at 23 ° C. and 50% RH Cured under 7 days. The 180 degree peel test was performed using a tensile tester (model strograph VE5D manufactured by Toyo Seiki Co., Ltd.) according to JIS K6854, and the peel adhesive strength (N / mm) was measured. Moreover, the surface state of the test piece after the fracture was visually observed. When the composition itself is destroyed, the surface condition is considered as being adhered to the polypropylene plate, and the evaluation is ○, and when the composition peels off from the polypropylene plate, the surface state is regarded as not being adhered to the polypropylene plate and evaluated. X. The results are shown in Table 1.
（結果）
表１に示すように、実験例１と５では、ポリプロピレン板に対して優れた接着性が得られた。実験例２，３，４，６では、分子量分布が１．５〜４．０の範囲にある塩素化ポリプロピレンを用いたが、融点が７０℃または８０℃と高く、接着強度は不十分であった。
(result)
As shown in Table 1, in Experimental Examples 1 and 5, excellent adhesion to the polypropylene plate was obtained. In Experimental Examples 2, 3, 4, and 6, chlorinated polypropylene having a molecular weight distribution in the range of 1.5 to 4.0 was used, but the melting point was as high as 70 ° C or 80 ° C, and the adhesive strength was insufficient. It was.
本発明の接着剤組成物によれば、ポリオレフィン等の難接着性基材に対して、プライマー処理が不要で、実用に耐えうる良好な接着強度を付与することが可能となるので、塗料、接着剤、インキ、シーリング剤等の用途において有用である。 According to the adhesive composition of the present invention, a primer treatment is not required for a difficult-to-adhere substrate such as polyolefin, and it is possible to impart good adhesive strength that can withstand practical use. Useful in applications such as adhesives, inks, and sealing agents.
Claims (3)
−ＳｉＲ３−ａＸａ （Ｉ）
（ここで、Ｒは、炭素数１〜２０のアルキル基、Ｘは水酸基または炭素数１〜６のアルコキシ基、ａは１、２または３である。） The adhesive composition according to claim 1, wherein the hydrolyzable silicon group is represented by the following general formula (I).
-SiR 3-a X a (I)
(Here, R is an alkyl group having 1 to 20 carbon atoms, X is a hydroxyl group or an alkoxy group having 1 to 6 carbon atoms, and a is 1, 2 or 3.)
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| JP2007269935A (en) * | 2006-03-31 | 2007-10-18 | Nogawa Chemical Co Ltd | Adhesive composition for adhering polyolefin |
| WO2007142067A1 (en) * | 2006-06-02 | 2007-12-13 | Kaneka Corporation | Curable composition |
| JP2013060589A (en) * | 2011-08-25 | 2013-04-04 | Cemedine Co Ltd | Room-temperature, moisture-curable adhesive composition |
| JP2013234235A (en) * | 2012-05-08 | 2013-11-21 | Konishi Co Ltd | Moisture-curable adhesive composition |
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| JP2007269935A (en) * | 2006-03-31 | 2007-10-18 | Nogawa Chemical Co Ltd | Adhesive composition for adhering polyolefin |
| WO2007142067A1 (en) * | 2006-06-02 | 2007-12-13 | Kaneka Corporation | Curable composition |
| JP2013060589A (en) * | 2011-08-25 | 2013-04-04 | Cemedine Co Ltd | Room-temperature, moisture-curable adhesive composition |
| JP2013234235A (en) * | 2012-05-08 | 2013-11-21 | Konishi Co Ltd | Moisture-curable adhesive composition |
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| WO2021132523A1 (en) * | 2019-12-27 | 2021-07-01 | 東洋紡株式会社 | Moisture-curable adhesive composition |
| CN114901776A (en) * | 2019-12-27 | 2022-08-12 | 东洋纺株式会社 | Moisture-curable adhesive composition |
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