JP6637436B2 - 樹脂改質用粒子、及びそれを含む塩化ビニル系樹脂組成物 - Google Patents
樹脂改質用粒子、及びそれを含む塩化ビニル系樹脂組成物 Download PDFInfo
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- JP6637436B2 JP6637436B2 JP2016556625A JP2016556625A JP6637436B2 JP 6637436 B2 JP6637436 B2 JP 6637436B2 JP 2016556625 A JP2016556625 A JP 2016556625A JP 2016556625 A JP2016556625 A JP 2016556625A JP 6637436 B2 JP6637436 B2 JP 6637436B2
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- resin
- vinyl chloride
- glycidyl group
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- 239000011347 resin Substances 0.000 title claims description 84
- 229920005989 resin Polymers 0.000 title claims description 84
- 239000002245 particle Substances 0.000 title claims description 83
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 title claims description 61
- 239000011342 resin composition Substances 0.000 title claims description 36
- 239000000178 monomer Substances 0.000 claims description 67
- 229920000642 polymer Polymers 0.000 claims description 62
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims description 58
- 229920001577 copolymer Polymers 0.000 claims description 40
- 239000004816 latex Substances 0.000 claims description 39
- 229920000126 latex Polymers 0.000 claims description 39
- 239000000203 mixture Substances 0.000 claims description 38
- 239000011258 core-shell material Substances 0.000 claims description 37
- 238000004519 manufacturing process Methods 0.000 claims description 30
- 239000003381 stabilizer Substances 0.000 claims description 24
- 239000002253 acid Substances 0.000 claims description 20
- 230000015271 coagulation Effects 0.000 claims description 20
- 238000005345 coagulation Methods 0.000 claims description 20
- 239000012792 core layer Substances 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 16
- 150000003839 salts Chemical class 0.000 claims description 14
- 239000010410 layer Substances 0.000 claims description 13
- 230000004048 modification Effects 0.000 claims description 13
- 238000012986 modification Methods 0.000 claims description 13
- 229920001971 elastomer Polymers 0.000 claims description 12
- 239000005060 rubber Substances 0.000 claims description 12
- 229920002554 vinyl polymer Polymers 0.000 claims description 9
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 5
- 238000005469 granulation Methods 0.000 claims description 5
- 230000003179 granulation Effects 0.000 claims description 5
- 229910052749 magnesium Inorganic materials 0.000 claims description 5
- 229910052791 calcium Inorganic materials 0.000 claims description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 50
- 229920002959 polymer blend Polymers 0.000 description 34
- -1 3,4-epoxycyclohexyl Chemical group 0.000 description 29
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 20
- 239000000701 coagulant Substances 0.000 description 18
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 12
- 238000012360 testing method Methods 0.000 description 11
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 10
- 238000011156 evaluation Methods 0.000 description 10
- 238000006116 polymerization reaction Methods 0.000 description 10
- 239000000843 powder Substances 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 9
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 8
- 125000000217 alkyl group Chemical group 0.000 description 8
- 150000001993 dienes Chemical class 0.000 description 8
- 238000002156 mixing Methods 0.000 description 8
- 238000000465 moulding Methods 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 7
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 7
- 239000004014 plasticizer Substances 0.000 description 7
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 6
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 5
- 229910019142 PO4 Inorganic materials 0.000 description 5
- 230000018044 dehydration Effects 0.000 description 5
- 238000006297 dehydration reaction Methods 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 239000003995 emulsifying agent Substances 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 239000010452 phosphate Substances 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 4
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 4
- 239000001110 calcium chloride Substances 0.000 description 4
- 229910001628 calcium chloride Inorganic materials 0.000 description 4
- 239000012986 chain transfer agent Substances 0.000 description 4
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 4
- 238000010556 emulsion polymerization method Methods 0.000 description 4
- 239000011777 magnesium Substances 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 230000000379 polymerizing effect Effects 0.000 description 4
- YAJYJWXEWKRTPO-UHFFFAOYSA-N 2,3,3,4,4,5-hexamethylhexane-2-thiol Chemical compound CC(C)C(C)(C)C(C)(C)C(C)(C)S YAJYJWXEWKRTPO-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 239000003109 Disodium ethylene diamine tetraacetate Substances 0.000 description 3
- ZGTMUACCHSMWAC-UHFFFAOYSA-L EDTA disodium salt (anhydrous) Chemical compound [Na+].[Na+].OC(=O)CN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O ZGTMUACCHSMWAC-UHFFFAOYSA-L 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 235000011054 acetic acid Nutrition 0.000 description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- 230000001112 coagulating effect Effects 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 235000019301 disodium ethylene diamine tetraacetate Nutrition 0.000 description 3
- 238000007720 emulsion polymerization reaction Methods 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 229920000915 polyvinyl chloride Polymers 0.000 description 3
- 239000004800 polyvinyl chloride Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 239000000523 sample Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 238000010558 suspension polymerization method Methods 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical group C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- PMBXCGGQNSVESQ-UHFFFAOYSA-N 1-Hexanethiol Chemical compound CCCCCCS PMBXCGGQNSVESQ-UHFFFAOYSA-N 0.000 description 2
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 2
- VVAAYFMMXYRORI-UHFFFAOYSA-N 4-butoxy-2-methylidene-4-oxobutanoic acid Chemical compound CCCCOC(=O)CC(=C)C(O)=O VVAAYFMMXYRORI-UHFFFAOYSA-N 0.000 description 2
- SXIFAEWFOJETOA-UHFFFAOYSA-N 4-hydroxy-butyl Chemical group [CH2]CCCO SXIFAEWFOJETOA-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Chemical compound CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- 229920002943 EPDM rubber Polymers 0.000 description 2
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 229920000459 Nitrile rubber Polymers 0.000 description 2
- 239000006057 Non-nutritive feed additive Substances 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 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 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- IHBCFWWEZXPPLG-UHFFFAOYSA-N [Ca].[Zn] Chemical compound [Ca].[Zn] IHBCFWWEZXPPLG-UHFFFAOYSA-N 0.000 description 2
- 229920000800 acrylic rubber Polymers 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- SHLNMHIRQGRGOL-UHFFFAOYSA-N barium zinc Chemical compound [Zn].[Ba] SHLNMHIRQGRGOL-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- GCTPMLUUWLLESL-UHFFFAOYSA-N benzyl prop-2-enoate Chemical compound C=CC(=O)OCC1=CC=CC=C1 GCTPMLUUWLLESL-UHFFFAOYSA-N 0.000 description 2
- SAOKZLXYCUGLFA-UHFFFAOYSA-N bis(2-ethylhexyl) adipate Chemical compound CCCCC(CC)COC(=O)CCCCC(=O)OCC(CC)CCCC SAOKZLXYCUGLFA-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
- WQAQPCDUOCURKW-UHFFFAOYSA-N butanethiol Chemical compound CCCCS WQAQPCDUOCURKW-UHFFFAOYSA-N 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229920003244 diene elastomer Polymers 0.000 description 2
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 229910001651 emery Inorganic materials 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 2
- XLYMOEINVGRTEX-UHFFFAOYSA-N fumaric acid monoethyl ester Natural products CCOC(=O)C=CC(O)=O XLYMOEINVGRTEX-UHFFFAOYSA-N 0.000 description 2
- NKHAVTQWNUWKEO-UHFFFAOYSA-N fumaric acid monomethyl ester Natural products COC(=O)C=CC(O)=O NKHAVTQWNUWKEO-UHFFFAOYSA-N 0.000 description 2
- 238000005227 gel permeation chromatography Methods 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 229910001629 magnesium chloride Inorganic materials 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- XWGJFPHUCFXLBL-UHFFFAOYSA-M rongalite Chemical compound [Na+].OCS([O-])=O XWGJFPHUCFXLBL-UHFFFAOYSA-M 0.000 description 2
- 229920002379 silicone rubber Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- UTOVMEACOLCUCK-SNAWJCMRSA-N (e)-4-butoxy-4-oxobut-2-enoic acid Chemical compound CCCCOC(=O)\C=C\C(O)=O UTOVMEACOLCUCK-SNAWJCMRSA-N 0.000 description 1
- XLYMOEINVGRTEX-ONEGZZNKSA-N (e)-4-ethoxy-4-oxobut-2-enoic acid Chemical compound CCOC(=O)\C=C\C(O)=O XLYMOEINVGRTEX-ONEGZZNKSA-N 0.000 description 1
- AYAUWVRAUCDBFR-ONEGZZNKSA-N (e)-4-oxo-4-propoxybut-2-enoic acid Chemical compound CCCOC(=O)\C=C\C(O)=O AYAUWVRAUCDBFR-ONEGZZNKSA-N 0.000 description 1
- AYAUWVRAUCDBFR-ARJAWSKDSA-N (z)-4-oxo-4-propoxybut-2-enoic acid Chemical compound CCCOC(=O)\C=C/C(O)=O AYAUWVRAUCDBFR-ARJAWSKDSA-N 0.000 description 1
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 description 1
- HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 1
- KTZVZZJJVJQZHV-UHFFFAOYSA-N 1-chloro-4-ethenylbenzene Chemical compound ClC1=CC=C(C=C)C=C1 KTZVZZJJVJQZHV-UHFFFAOYSA-N 0.000 description 1
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 description 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 1
- OMVSWZDEEGIJJI-UHFFFAOYSA-N 2,2,4-Trimethyl-1,3-pentadienol diisobutyrate Chemical compound CC(C)C(=O)OC(C(C)C)C(C)(C)COC(=O)C(C)C OMVSWZDEEGIJJI-UHFFFAOYSA-N 0.000 description 1
- JCTXKRPTIMZBJT-UHFFFAOYSA-N 2,2,4-trimethylpentane-1,3-diol Chemical compound CC(C)C(O)C(C)(C)CO JCTXKRPTIMZBJT-UHFFFAOYSA-N 0.000 description 1
- LDXJRKWFNNFDSA-UHFFFAOYSA-N 2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound C1CN(CC2=NNN=C21)CC(=O)N3CCN(CC3)C4=CN=C(N=C4)NCC5=CC(=CC=C5)OC(F)(F)F LDXJRKWFNNFDSA-UHFFFAOYSA-N 0.000 description 1
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- NKHAVTQWNUWKEO-NSCUHMNNSA-N monomethyl fumarate Chemical compound COC(=O)\C=C\C(O)=O NKHAVTQWNUWKEO-NSCUHMNNSA-N 0.000 description 1
- 229940005650 monomethyl fumarate Drugs 0.000 description 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical group CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000012875 nonionic emulsifier Substances 0.000 description 1
- 125000001400 nonyl 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])C([H])([H])[H] 0.000 description 1
- KZCOBXFFBQJQHH-UHFFFAOYSA-N octane-1-thiol Chemical compound CCCCCCCCS KZCOBXFFBQJQHH-UHFFFAOYSA-N 0.000 description 1
- 229940065472 octyl acrylate Drugs 0.000 description 1
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- QUPCNWFFTANZPX-UHFFFAOYSA-M paramenthane hydroperoxide Chemical compound [O-]O.CC(C)C1CCC(C)CC1 QUPCNWFFTANZPX-UHFFFAOYSA-M 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- JQCXWCOOWVGKMT-UHFFFAOYSA-N phthalic acid diheptyl ester Natural products CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC JQCXWCOOWVGKMT-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001485 poly(butyl acrylate) polymer Polymers 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
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- 238000002360 preparation method Methods 0.000 description 1
- FZYCEURIEDTWNS-UHFFFAOYSA-N prop-1-en-2-ylbenzene Chemical compound CC(=C)C1=CC=CC=C1.CC(=C)C1=CC=CC=C1 FZYCEURIEDTWNS-UHFFFAOYSA-N 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
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- 102200046998 rs62645894 Human genes 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000565 sealant Substances 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
- 230000035939 shock Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- VYGBQXDNOUHIBZ-UHFFFAOYSA-L sodium formaldehyde sulphoxylate Chemical compound [Na+].[Na+].O=C.[O-]S[O-] VYGBQXDNOUHIBZ-UHFFFAOYSA-L 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 125000004079 stearyl 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])C([H])([H])C([H])([H])C([H])([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
- 238000003860 storage Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- SJMYWORNLPSJQO-UHFFFAOYSA-N tert-butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)(C)C SJMYWORNLPSJQO-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- GEKDEMKPCKTKEC-UHFFFAOYSA-N tetradecane-1-thiol Chemical compound CCCCCCCCCCCCCCS GEKDEMKPCKTKEC-UHFFFAOYSA-N 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 239000003017 thermal stabilizer Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- 229910000404 tripotassium phosphate Inorganic materials 0.000 description 1
- 235000019798 tripotassium phosphate Nutrition 0.000 description 1
- KOWVWXQNQNCRRS-UHFFFAOYSA-N tris(2,4-dimethylphenyl) phosphate Chemical compound CC1=CC(C)=CC=C1OP(=O)(OC=1C(=CC(C)=CC=1)C)OC1=CC=C(C)C=C1C KOWVWXQNQNCRRS-UHFFFAOYSA-N 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
- C08F220/32—Esters containing oxygen in addition to the carboxy oxygen containing epoxy radicals
- C08F220/325—Esters containing oxygen in addition to the carboxy oxygen containing epoxy radicals containing glycidyl radical, e.g. glycidyl (meth)acrylate
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/04—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08L27/06—Homopolymers or copolymers of vinyl chloride
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/062—Copolymers with monomers not covered by C08L33/06
- C08L33/068—Copolymers with monomers not covered by C08L33/06 containing glycidyl groups
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/003—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/04—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to rubbers
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/08—Stabilised against heat, light or radiation or oxydation
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/06—Polymer mixtures characterised by other features having improved processability or containing aids for moulding methods
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- C—CHEMISTRY; METALLURGY
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- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2207/00—Properties characterising the ingredient of the composition
- C08L2207/53—Core-shell polymer
Description
さらに、本発明者は、好ましくは酸凝固剤や塩凝固剤の両方が所望の特性を呈する樹脂改質用粒子の調製に有効である事、より好ましくは酸凝固剤が所望の特性(特に樹脂表面のブツ低減)を呈する樹脂改質用粒子の調製に有効であることも見出した。
[1] グリシジル基含有重合体(B)とコアシェル共重合体(C)とを一粒子内に複合して含む樹脂改質用粒子。
[2] 前記グリシジル基含有重合体(B)が、グリシジル基含有エチレン性不飽和単量体(B1)50〜100重量%と、その他の不飽和単量体(B2)0〜50重量%の重合体である[1]に記載の樹脂改質用粒子。
[3] 前記コアシェル共重合体(C)が、ゴム弾性を有するコア層と、このコア層を被覆するビニル系重合体のシェル層とから構成されている[1]又は[2]に記載の樹脂改質用粒子。
[4] 前記グリシジル基含有重合体(B)の量が、グリシジル基含有重合体(B)とコアシェル共重合体(C)の合計100重量部に対して、1〜30重量部である[1]〜[3]のいずれかに記載の樹脂改質用粒子。
[5] Mg及びCaの含有量が、100ppm以下である[1]〜[4]のいずれかに記載の樹脂改質用粒子。
[6] 塩化ビニル系樹脂(A)と、[1]〜[5]のいずれかに記載の樹脂改質用粒子とを含有する塩化ビニル系樹脂組成物。
[7] 前記樹脂改質用粒子の量が、塩化ビニル系樹脂(A)100重量部に対して、1〜30重量部である[6]に記載の塩化ビニル系樹脂組成物。
[8] 錫系安定剤0.1〜3.0重量部をさらに含む[6]又は[7]に記載の塩化ビニル系樹脂組成物。
[9] グリシジル基含有重合体(B)とコアシェル共重合体(C)をラテックス状態で混合し、酸凝固あるいは塩凝固のいずれかの造粒方法により造粒することを特徴とする樹脂改質用粒子の製造方法。
[10] グリシジル基含有重合体(B)とコアシェル共重合体(C)をラテックス状態で混合し、酸凝固の造粒方法により造粒することを特徴とする[9]に記載の樹脂改質用粒子の製造方法。
[11] グリシジル基含有重合体(B)0.1〜10重量部、コアシェル共重合体(C)0.1〜20重量部を混合する[9]又は[10]に記載の樹脂改質用粒子の製造方法。
[12] 塩化ビニル系樹脂組成物(A)100質量部に対して、[9]〜[11]のいずれかに記載の製造方法で得られた樹脂改質用粒子1〜30重量部を含ませる塩化ビニル系樹脂組成物の製造方法。
[13] [6]〜[8]のいずれかに記載の塩化ビニル系樹脂組成物の成形体であって、成形体表面に現れる大きさ10μm以上1000μm以下の粒状物の個数が、20cm×20cm当たり600個以下である事を特徴とする成形体。
本発明の樹脂改質用粒子は、グリシジル基含有重合体(B)とコアシェル共重合体(C)とを一粒子内に複合して含む。樹脂改質用粒子は、後述される通り、グリシジル基含有重合体とコアシェル共重合体それぞれをラテックス状態で混合し、グリシジル基含有重合体とコアシェル共重合体が互いに複合した状態で凝固してなるものであり、グリシジル基含有重合体とコアシェル共重合体とは、ラテックス粒子サイズ(例えば、サブミクロンサイズ)のレベルで均一に混ざっており、この状態を本明細書では「複合」という。
本発明のグリシジル基含有重合体(B)は、グリシジル基含有エチレン性不飽和単量体(B1)50〜100重量%と、その他の不飽和単量体(B2)0〜50重量%の重合体であることが好ましい。
重量平均分子量は、例えばゲルパーミエーションクロマトグラフィー(東ソー(株)社製、HLC−8220GPC)を使用して求めることができる。
本発明のコアシェル共重合体(C)は、ゴム弾性を有するコア層と、このコア層を被覆するビニル系重合体のシェル層とから構成されていることが好ましく、前記コア層に前記シェル層がグラフト結合していることがより好ましい。前記コア層は、グラフト結合した前記シェル層により、一部又は全部が覆われていてもよい。
コア層は、多層構造であってもよく、この場合、各層の組成は、互いに相違していても同一であってもよい。
ジエン系単量体(C1−1)は、ブタジエン、イソプレン、クロロプレン等が好ましく、より好ましくはブタジエンである。
ジエン系単量体と共重合可能な単量体(C1−2)は、スチレン、α−メチルスチレン、ビニルナフタレン等の芳香族ビニル系単量体、(メタ)アクリロニトリル等のシアン化ビニル系単量体等であることが好ましい。
ジエン系単量体と、ジエン系単量体と共重合可能な単量体は、それぞれ1種又は2種以上を使用してもよい。
コア層は、架橋度を高める為に、多官能性単量体を用いて重合されていてもよい。多官能性単量体は、ジビニルベンゼン、(イソ)シアヌル酸トリアリル、(メタ)アクリル酸アリル、イタコン酸ジアリル、フタル酸ジアリル等であることが好ましい。
(メタ)アクリル酸エステル単量体(C1−3)は、(メタ)アクリル酸メチル、(メタ)アクリル酸エチル、(メタ)アクリル酸ブチル、(メタ)アクリル酸2−エチルヘキシル、(メタ)アクリル酸オクチル、(メタ)アクリル酸ドデシル等のアルキル基含有(メタ)アクリル酸エステル、(メタ)アクリル酸2−ヒドロキシエチル、(メタ)アクリル酸4−ヒドロキシブチル等の(メタ)アクリル酸ヒドロキシアルキルエステル等であることが好ましい。
(メタ)アクリル酸エステル単量体と共重合可能な単量体(C1−4)は、ジエン系単量体と共重合可能な単量体(C1−2)と同様であってもよい。
(メタ)アクリル酸エステル単量体と、(メタ)アクリル酸エステル単量体と共重合可能な単量体は、それぞれ1種又は2種以上で使用されてもよい。
他方、コア層は、アクリル系ゴムとシリコン系ゴムの複合ゴムであってもよく、ジメチルシロキサンゴムとブチルアクリレートゴムの複合ゴムであってもよい。
これら単量体と共重合可能な単量体(C2−2)は、アクリロニトリル、メタクリロニトリル等の(メタ)アクリロニトリル、スチレン、α−メチルスチレン等の芳香族ビニル単量体、塩化ビニル、臭化ビニル、フッ化ビニル等のハロゲンビニル単量体等であることが好ましい。
これら単量体は単独でまたは2種以上を混合して用いられる。特に、塩化ビニル系樹脂への分散性および粉体化の観点から、(メタ)アクリル酸アルキル、芳香族ビニル単量体が好ましく、メタクリル酸メチル、スチレン、アクリル酸n−ブチルの組み合わせが好ましい。
コア層が40重量%未満であると、耐衝撃性が充分発揮できない場合があり、コア層が99.9重量%超であると、組成物の粘度が高くなりすぎて作業性が悪化する場合がある。
中でも、塩化カルシウム、塩化マグネシウムが好ましい。
凝固剤をラテックス混合物に添加する場合、凝固剤の使用量は、ラテックス混合物100重量部に対して、例えば0.0001〜0.01重量部であり、好ましくは0.001〜0.01重量部である。
凝固剤の溶液をラテックス混合物に添加する場合、凝固剤溶液の濃度は、例えば0.1〜10重量%であり、好ましくは0.2〜5重量%である。
凝固したラテックス混合物は、熱処理、脱水、洗浄および乾燥等に供され、樹脂改質用粒子を調製することができる。
他方、コアシェル共重合体(C)の含有量が樹脂改質用粒子100重量%中、例えば70重量%以上、好ましくは80重量%以上、より好ましくは85重量以上であることが望ましい。
またあまりにも少ない場合には、塩化ビニル系樹脂組成物に対して充分な熱安定性効果が発現されないため、グリシジル基含有重合体(B)が例えば0.5重量%以上、好ましくは5.0重量%以上、すなわちコアシェル重合体(C)の含有量が例えば99.5重量%以下、好ましくは95.0重量%以下である。
体積平均粒子径は、例えば粒度分析計(日機装(株)社製、Nanotracwave)を使用して測定することができる。
本発明には、塩化ビニル系樹脂(A)に対し、グリシジル基含有重合体(B)及びコアシェル共重合体(C)をラテックス状態で混合、酸凝固あるいは塩凝固の造粒方法により造粒した重合体混合物(樹脂改質用粒子)を含むことを特徴とする塩化ビニル系樹脂組成物が一態様として包含される。
塩化ビニル系樹脂組成物は、塩化ビニル系樹脂(A)と、重合体混合物の前記樹脂改質用粒子とを含有する。
粒状物(ブツ)は、成形体の表面に肉眼が観察できる大きさ10μm以上1000μm以下のものを意味する。粒状物の個数は、20cm×20cm当たり580個以下であることが好ましく、より好ましくは560個以下、さらに好ましくは540個以下、さらにより好ましくは520個以下である。
測定試料をテトラヒドロフラン(THF)に溶解させ、その可溶分を、ポリスチレンを基準とするゲルパーミエーションクロマトグラフィー(東ソー(株)社製、HLC−8220GPC)を使用して、グリシジル基含有重合体(B)の重量平均分子量を求めた(試料溶液:試料20mg/THF10mL、測定温度:25℃、検出器:示差屈折系、注入量:1mL)。
0.01〜0.5μmの重合体である樹脂改質用粒子の体積平均粒子径は、粒度分析計(日機装(株)社製、Nanotracwave)を使用して546nmの波長の光散乱を用いて測定した。
得られる(B)と(C)の重合体混合物(樹脂改質用粒子)の粉末10部を、メチル錫メルカプト系安定剤((株)勝田化工製 商品名:TM−181FSJ)1.0部、加工助剤((株)カネカ製 商品名:カネエース(登録商標)PA−20)1.0部、内部滑剤(Emery Oleochemicals社製 商品名:GH4)0.5部及び外部滑剤(Emery Oleochemicals社製 商品名:G70S)0.4部を含む塩化ビニル樹脂(A1)((株)カネカ製 商品名:カネビニール(登録商標)S−1008 平均重合度800)100部に粉体状態で混合し、8インチテストロール(関西ロール(株)社製、テストロール)を用い、回転数17rpm、165℃で5分間混練りした後、180℃のプレスで15分間加圧、成形して厚さ1.0mmのプレス板を作製した。このプレス板より厚さ5.0mm、長さ70mm、幅15mmの2号Aのアイゾット衝撃試験用テストピースを作製した。得られたテストピースを用いてJIS K 7110規格に従い、0℃及び23℃における耐衝撃性を測定した。
耐衝撃性評価と同様の組成・条件でロール混練り、プレス成形により厚さ1.0mm、10×10mmの試験片を作成した。この試験片を恒温乾燥機(サタケ社製 熱風循環恒温乾燥機)にてJIS K 7212に従い、180℃、試験時間110分、吊り下げ方式で試験を行い、試験開始から10分毎に試験片を取り出し、色調のL値が20以下の値となる点を黒化と判断し、黒化までの時間を熱安定性として評価した。
上記熱安定性で使用した試料において、20cm×20cm面積に含まれるシート上の未ゲル化物の個数を目視で観察し、数を数えた。未ゲル化物は、成形体表面の大きさ10μm以上1000μm以下のブツとした。
あらかじめ水に溶解したジオクチルコハク酸ナトリウム0.8部(重量部、以下同様)および硫酸第一鉄(FeSO4・7H2O)0.0005部、エチレンジアミン四酢酸二ナトリウム塩0.002部、炭酸ナトリウム0.5部及びホルムアルデヒドスルホキシル酸ナトリウム0.055部を撹拌機付き反応器に入れ、さらに水を加えて水の全量を200部とした。反応器内をチッ素置換して空間部および水中の酸素を除去したのち、撹拌しつつ内容物を60℃まで昇温しつつ、メタクリル酸グリシジル85部、メタクリル酸メチル10部、スチレン5部、t−ドデシルメルカプタン0.5部及びt−ブチルハイドロパーオキサイド0.03部を連続追加しながら重合を行い、共重合成分の追加終了後もそのまま内容物を60℃に保ったまま撹拌を1時間以上続けて重合を完結させたのちに冷却し、グリシジル基含有重合体(B−1)のラテックスを得た。
製造例1−1と同様の方法で、表1で示す組成でもって乳化重合を行い、グリシジル基含有重合体(B−2〜B−6)を得た。
GMA:メタクリル酸グリシジル
MMA:メタクリル酸メチル
St:スチレン
tDM:t−ドデシルメルカプタン
耐圧重合機に水200部、オレイン酸ソーダ2.2部、硫酸第一鉄(FeSO4・7H2O)0.002部、エチレンジアミン四酢酸二ナトリウム塩0.007部、ホルムアルデヒドスルホキシル酸ソーダ0.08部、リン酸三カリウム0.4部、ブタジエン100部及びパラメンタンハイドロパーオキサイド0.1部を仕込み、これらを重合させてジエン系ゴム状重合体のラテックスを得た。このラテックス195部(固形分量70部)に、水20部、硫酸第一鉄0.003部、エチレンジアミン四酢酸二ナトリウム塩0.012部およびホルムアルデヒドスルホキシル酸ソーダ1.7部を添加し、これに60℃でスチレン4.5部、メタクリル酸メチル21部、アクリル酸n−ブチル4.5部及びt−ブチルハイドロパーオキサイド0.1部の混合液を連続追加してグラフト重合し、コアシェル共重合体(C−1)を得た。
Bd:ブタジエン
MMA:メタクリル酸メチル
St:スチレン
BA:アクリル酸n−ブチル
得られたグリシジル基含有重合体(B−1)のラテックス30部(固形分量10部)と前記コアシェル共重合体(C−1)のラテックス257部(固形分量90部)をラテックス状態で混合した(この時のグリシジル基含有重合体(B−1)とコアシェル共重合体(C−1)との重量比は10/90となる)。ラテックス状態の重合体混合物に25℃の温度条件下で1%に希釈した塩酸1部を加えて凝固を行ない、熱処理、脱水、洗浄および乾燥を行ない、重合体混合物(樹脂改質用粒子)(X1)を得た。
表3記載の(B−1)と(C−1)の重量比でもって混合したラテックス状態の重合体混合物に25℃の温度条件下で1%に希釈したリン酸1部を加えて凝固を行ない、熱処理、脱水、洗浄および乾燥を行ない、重合体混合物(樹脂改質用粒子)(X2)を得た。
表3記載の(B−1)と(C−1)の重量比でもって混合したラテックス状態の重合体混合物に25℃の温度条件下で1%に希釈した酢酸1部を加えて凝固を行ない、熱処理、脱水、洗浄および乾燥を行ない、重合体混合物(樹脂改質用粒子)(X3)を得た。
表3記載の(B−1)と(C−1)の重量比でもって混合したラテックス状態の重合体混合物に25℃の温度条件下で1%に希釈した硫酸1部を加えて凝固を行ない、熱処理、脱水、洗浄および乾燥を行ない、重合体混合物(樹脂改質用粒子)(X4)を得た。
表3記載の(B−1)と(C−1)の重量比でもって混合したラテックス状態の重合体混合物に25℃の温度条件下で1%に希釈した塩化カルシウム4部を加えて凝固を行ない、熱処理、脱水、洗浄および乾燥を行ない、重合体混合物(樹脂改質用粒子)(X5)を得た。
表3記載の(B−1)と(C−1)の重量比でもって、(B−1)は塩化カルシウム凝固、(C−1)は塩酸凝固によってそれぞれを単独に造粒したものを粉体状態で混合した重合体混合物(X6)を得た。
表3記載の(B−1)と(C−1)の重量比でもって混合したラテックス状態の重合体混合物をスプレードライヤー(大川原化工機(株)製、L−8型)を用いて、入り口温度130℃、出口温度60℃、アドマイザー回転数16000rpmにて噴霧乾燥した重合体混合物(X7)を得た。
塩化ビニル樹脂(A1)100部に対し、重合体混合物(樹脂改質用粒子)(X1)10部を添加した塩化ビニル樹脂組成物の物性を前記記載の評価項目によって評価を行った。結果を表4に示す。
実施例1において、重合体混合物(樹脂改質用粒子)(X1)に換えて、(X2)を添加した塩化ビニル樹脂組成物を調製し、当該組成物に対し、同様の評価を行った。結果を表4に示す。
実施例1において、重合体混合物(樹脂改質用粒子)(X1)に換えて、(X3)を添加した塩化ビニル樹脂組成物を調製し、当該組成物に対し、同様の評価を行った。結果を表4に示す。
実施例1において、重合体混合物(樹脂改質用粒子)(X1)に換えて、(X4)を添加した塩化ビニル樹脂組成物を調製し、当該組成物に対し、同様の評価を行った。結果を表4に示す。
実施例1において、重合体混合物(樹脂改質用粒子)(X1)に換えて、(X5)を添加した塩化ビニル樹脂組成物を調製し、当該組成物に対し、同様の評価を行った。結果を表4に示す。
実施例1において、重合体混合物(樹脂改質用粒子)(X1)に換えて、(X6)を添加した塩化ビニル樹脂組成物を調製し、当該組成物に対し、同様の評価を行った。結果を表4に示す。
実施例1において、重合体混合物(樹脂改質用粒子)(X1)に換えて、(X7)を添加した塩化ビニル樹脂組成物を調製し、当該組成物に対し、同様の評価を行った。結果を表4に示す。
得られる重合体混合物(樹脂改質用粒子)の粉末(X1)6部を、メチル錫メルカプト系安定剤(Dow Chemical社製 商品名:ADVANSTAB TM181)2.0部、加工助剤(Dow Chemical社製 商品名:PARALOIDK175)1.0部、安定剤(水澤化学工業(株)製 STABINEX DSM−1)3.6部、酸化防止剤(BASF社製 商品名:Irganox 175)0.3部および酸化チタン3.0部(Dupont社製 商品名:Ti−pure R−902+)を含む塩素化塩化ビニル樹脂(A2)((株)カネカ製 商品名:カネビニールH−829 平均重合度900)100部に粉体状態で混合し、8インチテストロール(関西ロール(株)社製、テストロール)を用い、回転数18rpm、190℃で5分間混練りした後、200℃のプレスで15分間加圧、成形して厚さ1.0mmのプレス板を作製した。このプレス成形板より、前記記載の23℃における耐衝撃性および熱安定性の評価法の条件でもって評価した。結果を表5に示す。
実施例6において、重合体混合物(樹脂改質用粒子)(X1)に換えて、コアシェル共重合体(C−1)の塩酸凝固物を添加した塩化ビニル樹脂組成物を調製し、当該組成物に対し、同様の評価を行った。結果を表5に示す。
Claims (12)
- グリシジル基含有重合体(B)とコアシェル共重合体(C)とを一粒子内に複合して含む酸凝固または塩凝固粒子であり、
前記グリシジル基含有重合体(B)が、グリシジル基含有エチレン性不飽和単量体(B1)50〜100重量%と、その他の不飽和単量体(B2)0〜50重量%の重合体である樹脂改質用粒子。 - 前記コアシェル共重合体(C)が、ゴム弾性を有するコア層と、このコア層を被覆するビニル系重合体のシェル層とから構成されている請求項1に記載の樹脂改質用粒子。
- 前記グリシジル基含有重合体(B)の量が、グリシジル基含有重合体(B)とコアシェル共重合体(C)の合計100重量部に対して、1〜30重量部である請求項1又は2のいずれかに記載の樹脂改質用粒子。
- Mg及びCaの含有量が、100ppm以下である請求項1〜3のいずれかに記載の樹脂改質用粒子。
- 塩化ビニル系樹脂(A)と、請求項1〜4のいずれかに記載の樹脂改質用粒子とを含有する塩化ビニル系樹脂組成物。
- 前記樹脂改質用粒子の量が、塩化ビニル系樹脂(A)100重量部に対して、1〜30重量部である請求項5に記載の塩化ビニル系樹脂組成物。
- 錫系安定剤0.1〜3.0重量部をさらに含む請求項5又は6に記載の塩化ビニル系樹脂組成物。
- グリシジル基含有エチレン性不飽和単量体(B1)50〜100重量%と、その他の不飽和単量体(B2)0〜50重量%の重合体であるグリシジル基含有重合体(B)とコアシェル共重合体(C)をラテックス状態で混合し、酸凝固あるいは塩凝固のいずれかの造粒方法により造粒することを特徴とする樹脂改質用粒子の製造方法。
- グリシジル基含有重合体(B)とコアシェル共重合体(C)をラテックス状態で混合し、酸凝固の造粒方法により造粒することを特徴とする請求項8に記載の樹脂改質用粒子の製造方法。
- グリシジル基含有重合体(B)0.1〜10重量部、コアシェル共重合体(C)0.1〜20重量部を混合する請求項8又は9に記載の樹脂改質用粒子の製造方法。
- 塩化ビニル系樹脂組成物(A)100重量部に対して、請求項8〜10のいずれかに記載の製造方法で得られた樹脂改質用粒子1〜30重量部を含ませる塩化ビニル系樹脂組成物の製造方法。
- 請求項5〜7のいずれかに記載の塩化ビニル系樹脂組成物の成形体であって、成形体表面に現れる大きさ10μm以上1000μm以下の粒状物の個数が、20cm×20cm当たり600個以下である事を特徴とする成形体。
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CN107075259B (zh) | 2020-09-04 |
JPWO2016068239A1 (ja) | 2017-08-17 |
EP3214137B1 (en) | 2019-10-23 |
CN107075259A (zh) | 2017-08-18 |
WO2016068239A1 (ja) | 2016-05-06 |
EP3214137A4 (en) | 2018-05-09 |
EP3214137A1 (en) | 2017-09-06 |
US10259937B2 (en) | 2019-04-16 |
US20170335097A1 (en) | 2017-11-23 |
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