JP6750673B2 - Bloom bleed inhibitor, composition containing the same, and elastomer molded article - Google Patents
Bloom bleed inhibitor, composition containing the same, and elastomer molded article Download PDFInfo
- Publication number
- JP6750673B2 JP6750673B2 JP2018514142A JP2018514142A JP6750673B2 JP 6750673 B2 JP6750673 B2 JP 6750673B2 JP 2018514142 A JP2018514142 A JP 2018514142A JP 2018514142 A JP2018514142 A JP 2018514142A JP 6750673 B2 JP6750673 B2 JP 6750673B2
- Authority
- JP
- Japan
- Prior art keywords
- bloom
- elastomer
- bleed
- molded article
- structural unit
- 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.)
- Expired - Fee Related
Links
- 229920001971 elastomer Polymers 0.000 title claims description 85
- 239000000806 elastomer Substances 0.000 title claims description 54
- 239000000203 mixture Substances 0.000 title claims description 46
- 239000003112 inhibitor Substances 0.000 title claims description 45
- -1 diene compound Chemical class 0.000 claims description 28
- 239000000843 powder Substances 0.000 claims description 27
- 239000003795 chemical substances by application Substances 0.000 claims description 26
- 150000001875 compounds Chemical class 0.000 claims description 21
- 238000013329 compounding Methods 0.000 claims description 14
- 229920001577 copolymer Polymers 0.000 claims description 13
- 230000000740 bleeding effect Effects 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 10
- 229910010272 inorganic material Inorganic materials 0.000 claims description 9
- 239000011147 inorganic material Substances 0.000 claims description 9
- 238000002441 X-ray diffraction Methods 0.000 claims description 8
- 229920002554 vinyl polymer Polymers 0.000 claims description 5
- 238000000634 powder X-ray diffraction Methods 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 3
- 238000005259 measurement Methods 0.000 claims description 3
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 31
- 239000005060 rubber Substances 0.000 description 31
- 239000002994 raw material Substances 0.000 description 27
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 16
- 239000011787 zinc oxide Substances 0.000 description 16
- 235000014692 zinc oxide Nutrition 0.000 description 16
- 229920005989 resin Polymers 0.000 description 14
- 239000011347 resin Substances 0.000 description 14
- 230000000694 effects Effects 0.000 description 13
- 229910052751 metal Inorganic materials 0.000 description 13
- 239000002184 metal Substances 0.000 description 13
- 239000002245 particle Substances 0.000 description 12
- 238000012360 testing method Methods 0.000 description 12
- 229920000642 polymer Polymers 0.000 description 9
- 238000004073 vulcanization Methods 0.000 description 9
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 8
- 239000005977 Ethylene Substances 0.000 description 8
- 239000000654 additive Substances 0.000 description 8
- 239000003963 antioxidant agent Substances 0.000 description 7
- 239000004014 plasticizer Substances 0.000 description 6
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 5
- 230000000996 additive effect Effects 0.000 description 5
- 239000004611 light stabiliser Substances 0.000 description 5
- 239000010734 process oil Substances 0.000 description 5
- 239000004711 α-olefin Substances 0.000 description 5
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 4
- 229910004298 SiO 2 Inorganic materials 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- 150000001340 alkali metals Chemical group 0.000 description 4
- 230000003078 antioxidant effect Effects 0.000 description 4
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000003431 cross linking reagent Substances 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- 239000006057 Non-nutritive feed additive Substances 0.000 description 3
- 230000003712 anti-aging effect Effects 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 229920003244 diene elastomer Polymers 0.000 description 3
- 150000001993 dienes Chemical class 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 3
- 239000003063 flame retardant Substances 0.000 description 3
- 150000001451 organic peroxides Chemical class 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 150000003464 sulfur compounds Chemical class 0.000 description 3
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical class CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 2
- 244000043261 Hevea brasiliensis Species 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- HXKCUQDTMDYZJD-UHFFFAOYSA-N Methyl selenac Chemical compound CN(C)C(=S)S[Se](SC(=S)N(C)C)(SC(=S)N(C)C)SC(=S)N(C)C HXKCUQDTMDYZJD-UHFFFAOYSA-N 0.000 description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical class C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- DZCCLNYLUGNUKQ-UHFFFAOYSA-N n-(4-nitrosophenyl)hydroxylamine Chemical class ONC1=CC=C(N=O)C=C1 DZCCLNYLUGNUKQ-UHFFFAOYSA-N 0.000 description 2
- 229920003052 natural elastomer Polymers 0.000 description 2
- 229920001194 natural rubber Polymers 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920001084 poly(chloroprene) Polymers 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920005672 polyolefin resin Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 230000001629 suppression Effects 0.000 description 2
- 229920003051 synthetic elastomer Polymers 0.000 description 2
- 239000005061 synthetic rubber Substances 0.000 description 2
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 2
- 229920003046 tetrablock copolymer Polymers 0.000 description 2
- 229960002447 thiram Drugs 0.000 description 2
- 229920000428 triblock copolymer Polymers 0.000 description 2
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- PRBHEGAFLDMLAL-GQCTYLIASA-N (4e)-hexa-1,4-diene Chemical compound C\C=C\CC=C PRBHEGAFLDMLAL-GQCTYLIASA-N 0.000 description 1
- RIPYNJLMMFGZSX-UHFFFAOYSA-N (5-benzoylperoxy-2,5-dimethylhexan-2-yl) benzenecarboperoxoate Chemical compound C=1C=CC=CC=1C(=O)OOC(C)(C)CCC(C)(C)OOC(=O)C1=CC=CC=C1 RIPYNJLMMFGZSX-UHFFFAOYSA-N 0.000 description 1
- JAEZSIYNWDWMMN-UHFFFAOYSA-N 1,1,3-trimethylthiourea Chemical compound CNC(=S)N(C)C JAEZSIYNWDWMMN-UHFFFAOYSA-N 0.000 description 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- FUPAJKKAHDLPAZ-UHFFFAOYSA-N 1,2,3-triphenylguanidine Chemical compound C=1C=CC=CC=1NC(=NC=1C=CC=CC=1)NC1=CC=CC=C1 FUPAJKKAHDLPAZ-UHFFFAOYSA-N 0.000 description 1
- JSCFNQDWXBNVBP-UHFFFAOYSA-N 1,2-diphenylguanidine;phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O.C=1C=CC=CC=1N=C(N)NC1=CC=CC=C1 JSCFNQDWXBNVBP-UHFFFAOYSA-N 0.000 description 1
- OWRCNXZUPFZXOS-UHFFFAOYSA-N 1,3-diphenylguanidine Chemical compound C=1C=CC=CC=1NC(=N)NC1=CC=CC=C1 OWRCNXZUPFZXOS-UHFFFAOYSA-N 0.000 description 1
- 150000005208 1,4-dihydroxybenzenes Chemical class 0.000 description 1
- XQUPVDVFXZDTLT-UHFFFAOYSA-N 1-[4-[[4-(2,5-dioxopyrrol-1-yl)phenyl]methyl]phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C(C=C1)=CC=C1CC1=CC=C(N2C(C=CC2=O)=O)C=C1 XQUPVDVFXZDTLT-UHFFFAOYSA-N 0.000 description 1
- KPAPHODVWOVUJL-UHFFFAOYSA-N 1-benzofuran;1h-indene Chemical compound C1=CC=C2CC=CC2=C1.C1=CC=C2OC=CC2=C1 KPAPHODVWOVUJL-UHFFFAOYSA-N 0.000 description 1
- PPWUTZVGSFPZOC-UHFFFAOYSA-N 1-methyl-2,3,3a,4-tetrahydro-1h-indene Chemical compound C1C=CC=C2C(C)CCC21 PPWUTZVGSFPZOC-UHFFFAOYSA-N 0.000 description 1
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 description 1
- ODBCKCWTWALFKM-UHFFFAOYSA-N 2,5-bis(tert-butylperoxy)-2,5-dimethylhex-3-yne Chemical compound CC(C)(C)OOC(C)(C)C#CC(C)(C)OOC(C)(C)C ODBCKCWTWALFKM-UHFFFAOYSA-N 0.000 description 1
- DMWVYCCGCQPJEA-UHFFFAOYSA-N 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane Chemical compound CC(C)(C)OOC(C)(C)CCC(C)(C)OOC(C)(C)C DMWVYCCGCQPJEA-UHFFFAOYSA-N 0.000 description 1
- 150000003923 2,5-pyrrolediones Chemical class 0.000 description 1
- GSFSVEDCYBDIGW-UHFFFAOYSA-N 2-(1,3-benzothiazol-2-yl)-6-chlorophenol Chemical compound OC1=C(Cl)C=CC=C1C1=NC2=CC=CC=C2S1 GSFSVEDCYBDIGW-UHFFFAOYSA-N 0.000 description 1
- UXYAMCDGZODWNV-UHFFFAOYSA-N 2-(2,4-dinitrophenyl)sulfanyl-1,3-thiazole Chemical class [N+](=O)([O-])C1=C(C=CC(=C1)[N+](=O)[O-])SC=1SC=CN1 UXYAMCDGZODWNV-UHFFFAOYSA-N 0.000 description 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- CPGFMWPQXUXQRX-UHFFFAOYSA-N 3-amino-3-(4-fluorophenyl)propanoic acid Chemical compound OC(=O)CC(N)C1=CC=C(F)C=C1 CPGFMWPQXUXQRX-UHFFFAOYSA-N 0.000 description 1
- BUZICZZQJDLXJN-UHFFFAOYSA-N 3-azaniumyl-4-hydroxybutanoate Chemical compound OCC(N)CC(O)=O BUZICZZQJDLXJN-UHFFFAOYSA-N 0.000 description 1
- MHKLKWCYGIBEQF-UHFFFAOYSA-N 4-(1,3-benzothiazol-2-ylsulfanyl)morpholine Chemical compound C1COCCN1SC1=NC2=CC=CC=C2S1 MHKLKWCYGIBEQF-UHFFFAOYSA-N 0.000 description 1
- HLBZWYXLQJQBKU-UHFFFAOYSA-N 4-(morpholin-4-yldisulfanyl)morpholine Chemical compound C1COCCN1SSN1CCOCC1 HLBZWYXLQJQBKU-UHFFFAOYSA-N 0.000 description 1
- RMDKEBZUCHXUER-UHFFFAOYSA-N 4-methylbicyclo[2.2.1]hept-2-ene Chemical compound C1CC2C=CC1(C)C2 RMDKEBZUCHXUER-UHFFFAOYSA-N 0.000 description 1
- CBNXGQUIJRGZRX-UHFFFAOYSA-N 5-[4-fluoro-3-(trifluoromethyl)phenyl]furan-2-carbaldehyde Chemical compound C1=C(C(F)(F)F)C(F)=CC=C1C1=CC=C(C=O)O1 CBNXGQUIJRGZRX-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 238000004438 BET method Methods 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- PDQAZBWRQCGBEV-UHFFFAOYSA-N Ethylenethiourea Chemical compound S=C1NCCN1 PDQAZBWRQCGBEV-UHFFFAOYSA-N 0.000 description 1
- KFFQABQEJATQAT-UHFFFAOYSA-N N,N'-dibutylthiourea Chemical compound CCCCNC(=S)NCCCC KFFQABQEJATQAT-UHFFFAOYSA-N 0.000 description 1
- FLVIGYVXZHLUHP-UHFFFAOYSA-N N,N'-diethylthiourea Chemical compound CCNC(=S)NCC FLVIGYVXZHLUHP-UHFFFAOYSA-N 0.000 description 1
- FCSHMCFRCYZTRQ-UHFFFAOYSA-N N,N'-diphenylthiourea Chemical compound C=1C=CC=CC=1NC(=S)NC1=CC=CC=C1 FCSHMCFRCYZTRQ-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical class OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 241000872198 Serjania polyphylla Species 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- PVMNBWXRCLEDCL-UHFFFAOYSA-N acetaldehyde;aniline Chemical compound CC=O.NC1=CC=CC=C1 PVMNBWXRCLEDCL-UHFFFAOYSA-N 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000001342 alkaline earth metals Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- ARCGXLSVLAOJQL-UHFFFAOYSA-N anhydrous trimellitic acid Natural products OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- 229910052792 caesium Inorganic materials 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
- 150000001869 cobalt compounds Chemical class 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 229920000359 diblock copolymer Polymers 0.000 description 1
- PGAXJQVAHDTGBB-UHFFFAOYSA-N dibutylcarbamothioylsulfanyl n,n-dibutylcarbamodithioate Chemical compound CCCCN(CCCC)C(=S)SSC(=S)N(CCCC)CCCC PGAXJQVAHDTGBB-UHFFFAOYSA-N 0.000 description 1
- 229940116901 diethyldithiocarbamate Drugs 0.000 description 1
- LMBWSYZSUOEYSN-UHFFFAOYSA-N diethyldithiocarbamic acid Chemical compound CCN(CC)C(S)=S LMBWSYZSUOEYSN-UHFFFAOYSA-N 0.000 description 1
- FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 description 1
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 1
- PXJJSXABGXMUSU-UHFFFAOYSA-N disulfur dichloride Chemical compound ClSSCl PXJJSXABGXMUSU-UHFFFAOYSA-N 0.000 description 1
- 150000004659 dithiocarbamates Chemical class 0.000 description 1
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical compound CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000010097 foam moulding Methods 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000004312 hexamethylene tetramine Substances 0.000 description 1
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 229910052745 lead Inorganic materials 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- ILSQBBRAYMWZLQ-UHFFFAOYSA-N n-(1,3-benzothiazol-2-ylsulfanyl)-n-propan-2-ylpropan-2-amine Chemical compound C1=CC=C2SC(SN(C(C)C)C(C)C)=NC2=C1 ILSQBBRAYMWZLQ-UHFFFAOYSA-N 0.000 description 1
- DEQZTKGFXNUBJL-UHFFFAOYSA-N n-(1,3-benzothiazol-2-ylsulfanyl)cyclohexanamine Chemical compound C1CCCCC1NSC1=NC2=CC=CC=C2S1 DEQZTKGFXNUBJL-UHFFFAOYSA-N 0.000 description 1
- 229940032017 n-oxydiethylene-2-benzothiazole sulfenamide Drugs 0.000 description 1
- 150000005002 naphthylamines Chemical class 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N o-dicarboxybenzene Natural products OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 150000004989 p-phenylenediamines Chemical class 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000010690 paraffinic oil Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical class OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920003192 poly(bis maleimide) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001296 polysiloxane Chemical class 0.000 description 1
- 239000005373 porous glass Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellityc acid Natural products OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 description 1
- 125000002943 quinolinyl group Chemical class N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- FWMUJAIKEJWSSY-UHFFFAOYSA-N sulfur dichloride Chemical compound ClSCl FWMUJAIKEJWSSY-UHFFFAOYSA-N 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229910052714 tellurium Inorganic materials 0.000 description 1
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 150000003585 thioureas Chemical class 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 239000004636 vulcanized rubber Substances 0.000 description 1
- 239000012991 xanthate Substances 0.000 description 1
- BOXSVZNGTQTENJ-UHFFFAOYSA-L zinc dibutyldithiocarbamate Chemical compound [Zn+2].CCCCN(C([S-])=S)CCCC.CCCCN(C([S-])=S)CCCC BOXSVZNGTQTENJ-UHFFFAOYSA-L 0.000 description 1
- NEYNBSGIXOOZGZ-UHFFFAOYSA-L zinc;butoxymethanedithioate Chemical compound [Zn+2].CCCCOC([S-])=S.CCCCOC([S-])=S NEYNBSGIXOOZGZ-UHFFFAOYSA-L 0.000 description 1
- PZKZVLYBWITYEF-UHFFFAOYSA-L zinc;n,n-diethylcarbamothioate Chemical compound [Zn+2].CCN(CC)C([O-])=S.CCN(CC)C([O-])=S PZKZVLYBWITYEF-UHFFFAOYSA-L 0.000 description 1
- LAGTXXPOZSLGSF-UHFFFAOYSA-L zinc;n-butyl-n-phenylcarbamodithioate Chemical compound [Zn+2].CCCCN(C([S-])=S)C1=CC=CC=C1.CCCCN(C([S-])=S)C1=CC=CC=C1 LAGTXXPOZSLGSF-UHFFFAOYSA-L 0.000 description 1
- KMNUDJAXRXUZQS-UHFFFAOYSA-L zinc;n-ethyl-n-phenylcarbamodithioate Chemical compound [Zn+2].CCN(C([S-])=S)C1=CC=CC=C1.CCN(C([S-])=S)C1=CC=CC=C1 KMNUDJAXRXUZQS-UHFFFAOYSA-L 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/32—Phosphorus-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
- C08K3/013—Fillers, pigments or reinforcing additives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L21/00—Compositions of unspecified rubbers
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
本発明は、ゴム、エラストマー等と併含する原料組成物を用いて得られた成形品(以下、「エラストマー成形品」という)から、配合剤のブリード又はブルームを抑制するブルーム・ブリード抑制剤に関する。 TECHNICAL FIELD The present invention relates to a bloom/bleed inhibitor for suppressing bleeding or bloom of a compounding agent from a molded article (hereinafter, referred to as “elastomer molded article”) obtained by using a raw material composition containing rubber, elastomer and the like. ..
従来、エラストマー成形品の形成に用いる原料組成物には、ゴム、エラストマー等の他に、要求性能に応じて、種々の添加剤が配合されている。例えば、ゴムを主とする場合には、プロセスオイル、加工助剤、老化防止剤、加硫促進剤等が配合され、エラストマーを主とする場合には、酸化防止剤、光安定剤、可塑剤等が配合される。
近年、エラストマー成形品の各種性能が向上する中、経時により添加剤が表出する現象が見られることがあった。このようなブルーム・ブリード現象は、外観性を低下させるだけでなく、初期物性が維持できなかったり、エラストマー成形品どうし、又は、エラストマー成形品と包装材料等とが接着してしまったりする不具合をもたらした。そこで、これらの不具合を抑制するために、原料組成物に、新たな添加剤を配合する試みがなされてきた。Conventionally, a raw material composition used for forming an elastomer molded article contains various additives in addition to rubber, elastomer and the like, depending on required performance. For example, in the case of mainly rubber, a process oil, a processing aid, an antioxidant, a vulcanization accelerator, etc. are blended, and in the case of mainly elastomer, an antioxidant, a light stabilizer, a plasticizer. And so on.
In recent years, while various performances of elastomer molded products have been improved, there have been cases where an additive is exposed over time. Such a phenomenon of blooming and bleeding not only deteriorates the appearance, but also cannot maintain the initial physical properties, or the elastomer molded products may adhere to each other, or the elastomer molded product and the packaging material may adhere to each other. Brought. Therefore, in order to suppress these problems, attempts have been made to add new additives to the raw material composition.
特許文献1には、エチレン、プロピレン及び非共役ジエンからなるエチレン・プロピレンゴムを含むゴム基材100重量部あたり、0〜150重量部のプロセスオイル及び加硫ゴム硬度70以上とするに十分なカーボンブラック又はカーボンブラックを主体とする充填剤を含み、0.01〜10重量部のジチオ酸塩化合物を加硫促進剤として用いるゴム組成物において、0.1〜15重量部の非反応性フェノールホルムアルデヒド樹脂又はポリエチレングリコールを添加することを特徴とする硫黄加硫可能な高硬度ゴム組成物が開示されている。
特許文献2には、硫黄系加硫剤と、場合により加硫促進剤とを含有するエチレン・プロピレン・ジエン三元共重合体とを基体とするゴムに、基体ゴム100重量部あたり特定構造を有するジチオリン酸亜鉛化合物を0.2〜10.0重量部配合してなることを特徴とするブルーム現象の改善されたゴム組成物が開示されている。
特許文献3には、その表面及び細孔内に老化防止剤を付着させた多孔質ガラス繊維をゴム配合中に配合されていることを特徴とする老化防止剤によるブルームを抑制したゴム製品が開示されている。
特許文献4には、天然ゴム、ジエン系合成ゴム又はエチレン・プロピレンゴムを主とする原料組成物に配合されるブリード・ブルーム防止剤として、特定構造を有する第4級アンモニウム塩化合物からなるものが開示されている。
特許文献5には、天然ゴム又は合成ゴムを主とする原料組成物に配合されるブルーム防止剤として、エチレン・飽和カルボン酸ビニルエステル共重合体けん化物のアルキレンオキサイド付加物と、ポリエーテル化合物とからなるものが開示されている。
また、特許文献6には、ポリオレフィン系樹脂を含む樹脂100重量部、層状珪酸塩0.1〜20重量部、並びに、ヒンダードアミン系光安定剤及び/又は紫外線吸収剤0.01〜5重量部を含有し、層状珪酸塩は、層状結晶の少なくとも一部の単層同士が単層表面の中心をずらせて重なりあって、見掛け上、厚さ5〜50nm、長さ500nm以上の平板状となって分散していることを特徴とする耐候性樹脂組成物が開示されている。In Patent Document 1, 0 to 150 parts by weight of a process oil and a vulcanized rubber having a hardness of 70 or more per 100 parts by weight of a rubber base material containing an ethylene/propylene rubber composed of ethylene, propylene and a non-conjugated diene are used. In a rubber composition containing a filler mainly composed of black or carbon black and using 0.01 to 10 parts by weight of a dithioate compound as a vulcanization accelerator, 0.1 to 15 parts by weight of non-reactive phenol formaldehyde is used. A sulfur-vulcanizable high-hardness rubber composition characterized by adding a resin or polyethylene glycol is disclosed.
Patent Document 2 discloses a rubber based on an ethylene/propylene/diene terpolymer containing a sulfur-based vulcanizing agent and optionally a vulcanization accelerator, with a specific structure per 100 parts by weight of the base rubber. Disclosed is a rubber composition having an improved bloom phenomenon, which is characterized by comprising 0.2 to 10.0 parts by weight of the zinc dithiophosphate compound.
Patent Document 3 discloses a rubber product in which bloom due to an anti-aging agent is suppressed, wherein porous glass fibers having an anti-aging agent attached to the surface and pores thereof are compounded in a rubber compound. Has been done.
Patent Document 4 discloses a bleeding/bloom preventing agent which is blended in a raw material composition mainly composed of natural rubber, diene-based synthetic rubber or ethylene/propylene rubber, and which comprises a quaternary ammonium salt compound having a specific structure. It is disclosed.
Patent Document 5 discloses an ethylene/saturated carboxylic acid vinyl ester copolymer saponified alkylene oxide adduct and a polyether compound as a bloom inhibitor mixed in a raw material composition mainly composed of natural rubber or synthetic rubber. Are disclosed.
Further, in Patent Document 6, 100 parts by weight of a resin containing a polyolefin resin, 0.1 to 20 parts by weight of a layered silicate, and 0.01 to 5 parts by weight of a hindered amine light stabilizer and/or an ultraviolet absorber. The layered silicate contains at least a part of the monolayers of the layered crystals overlapping with each other by shifting the centers of the monolayer surfaces, and apparently becomes a flat plate having a thickness of 5 to 50 nm and a length of 500 nm or more. A weather-resistant resin composition characterized by being dispersed is disclosed.
本発明の課題は、エラストマー成形品から、配合剤のブリード又はブルームの抑制効果に優れたブルーム・ブリード抑制剤及びそれを含む組成物並びにエラストマー成形品を提供することである。 An object of the present invention is to provide, from an elastomer molded article, a bloom/bleed inhibitor having an excellent effect of suppressing bleeding or bloom of a compounding agent, a composition containing the same, and an elastomer molded article.
本発明者は、非晶質の無機材料からなる粉末を含有する原料組成物を用いると、得られるエラストマー成形品において、添加剤等の配合剤に関わるブルーム・ブリード現象の発生が抑制されたことを見い出し、本発明を完成するに至った。
本発明は、以下に示される。
1.エラストマー成形品から配合剤のブリード又はブルームを抑制する材料であって、非晶質の無機材料からなる粉末を含有するブルーム・ブリード抑制剤。
2.上記無機材料が、下記一般式(1)で表される化合物である上記項1に記載のブルーム・ブリード抑制剤。
aM1 2O・bM2O・cM3 2O3・dM4O2・eP2O5・fH2O (1)
(式中、M1はアルカリ金属原子、M2は2価の金属原子、M3は3価の金属原子、M4は4価の金属原子であり、a、b、c、d及びeのうち、少なくとも1つは正数であり、残りは0又は正数であり、fは正数である。)
3.上記一般式(1)におけるM2OがZnOである上記項2に記載のブルーム・ブリード抑制剤。
4.上記一般式(1)におけるM3 2O3がAl2O3である上記項2に記載のブルーム・ブリード抑制剤。
5.上記粉末の比表面積が30g/m2以上である上記項1乃至4のいずれか一項に記載のブルーム・ブリード抑制剤。
6.上記項1乃至5のいずれか一項に記載のブルーム・ブリード抑制剤と、エラストマー又は未架橋ゴムとを含有する組成物であって、
上記ブルーム・ブリード抑制剤の含有量が、上記組成物の全体に対して0.5〜10質量%である組成物。
7.上記項6に記載の組成物から得られたエラストマー成形品。
8.上記項1乃至5のいずれか一項に記載のブルーム・ブリード抑制剤を用いて、エラストマー成形品から配合剤のブリード又はブルームを抑制する方法。The inventor of the present invention used the raw material composition containing a powder of an amorphous inorganic material, and in the obtained elastomer molded article, the occurrence of the bloom bleed phenomenon associated with the compounding agent such as an additive was suppressed. The present invention has been completed and the present invention has been completed.
The present invention is shown below.
1. A material for suppressing bleeding or bloom of a compounding agent from an elastomer molded article, which comprises a powder made of an amorphous inorganic material.
2. The bloom bleed inhibitor according to item 1, wherein the inorganic material is a compound represented by the following general formula (1).
aM 1 2 O·bM 2 O·cM 3 2 O 3 ·dM 4 O 2 ·eP 2 O 5 ·fH 2 O (1)
(In the formula, M 1 is an alkali metal atom, M 2 is a divalent metal atom, M 3 is a trivalent metal atom, M 4 is a tetravalent metal atom, and each of a, b, c, d and e Among them, at least one is a positive number, the rest are 0 or a positive number, and f is a positive number.)
3. Item 3. The bloom bleed inhibitor according to Item 2, wherein M 2 O in the general formula (1) is ZnO.
4. Item 3. The bloom bleed inhibitor according to Item 2, wherein M 3 2 O 3 in the general formula (1) is Al 2 O 3 .
5. Item 5. The bloom bleed inhibitor according to any one of Items 1 to 4, wherein the powder has a specific surface area of 30 g/m 2 or more.
6. A composition comprising the bloom bleed inhibitor according to any one of the above items 1 to 5 and an elastomer or an uncrosslinked rubber,
A composition in which the content of the bloom/bleed inhibitor is 0.5 to 10% by mass based on the entire composition.
7. An elastomer molded article obtained from the composition according to item 6.
8. A method for suppressing bleeding or blooming of a compounding agent from an elastomer molded article, using the bloom bleeding inhibitor according to any one of items 1 to 5 above.
本発明において、エラストマー成形品は、エラストマー又は未架橋ゴムを主とし、必要に応じて、樹脂を含有してもよい原料組成物(本発明の組成物)を用いて得られた成形品であり、原料組成物に含まれる配合剤の種類によっては、エラストマー成形品が架橋物からなる場合と、非架橋物からなる場合とがある。 In the present invention, the elastomer molded article is a molded article obtained by using a raw material composition (composition of the present invention) mainly containing an elastomer or uncrosslinked rubber and optionally containing a resin. Depending on the type of compounding agent contained in the raw material composition, the elastomer molded article may be a crosslinked product or a non-crosslinked product.
本発明のブルーム・ブリード抑制剤によれば、ブルーム・ブリード現象の発生が抑制されるエラストマー成形品を与えることができる。
本発明の組成物は、非晶質無機粉末からなるブルーム・ブリード抑制剤を含有するため、ブルーム・ブリード現象の発生が抑制されるエラストマー成形品の形成に好適である。また、組成物を用いてエラストマー成形品を製造する際に、変質、分解等を引き起こすことなく、また、他の成分と反応することなく、所定形状のエラストマー成形品を効率的よく製造することができる。
本発明のエラストマー成形品は、非晶質無機粉末からなるブルーム・ブリード抑制剤を含有するため、使用又は保管における経時によるブルーム・ブリード現象が発生しにくく、長期に渡って外観性に優れる。The bloom bleed inhibitor of the present invention can provide an elastomer molded article in which the occurrence of the bloom bleed phenomenon is suppressed.
Since the composition of the present invention contains a bloom bleed inhibitor composed of an amorphous inorganic powder, it is suitable for forming an elastomer molded article in which the occurrence of the bloom bleed phenomenon is suppressed. Further, when producing an elastomer molded article using the composition, it is possible to efficiently produce an elastomer molded article having a predetermined shape without causing alteration, decomposition, etc. and without reacting with other components. it can.
Since the elastomer molded article of the present invention contains the bloom bleed inhibitor composed of an amorphous inorganic powder, the bloom bleed phenomenon is less likely to occur over time during use or storage, and has excellent appearance over a long period of time.
以下、本発明を詳細に説明する。
本発明のブルーム・ブリード抑制剤は、非晶質の無機材料からなる粉末(以下、「非晶質無機粉末」という)を含有する。本発明のブルーム・ブリード抑制剤は、非晶質無機粉末のみからなるものであってよいし、ブルーム・ブリード現象の発生を抑制する限りにおいて、非晶質無機粉末と、他の粉末とからなるものであってもよい。
本発明において、非晶質とは、粉末X線回折測定により得られたX線回折像において検出されるピークが認められないか、又は、認められてもピークの半値幅が0.5degree以上の低結晶質のものである。図1は、非晶質無機材料の一種である、0.01Al2O3・ZnO・0.05H2Oからなる粉末のX線回折像であり、31.7degreeにおける特徴的な回折ピークの半値幅Hを求める方法を示す概略図であり、Hが約0.8degreeであることを示す。Hereinafter, the present invention will be described in detail.
The bloom bleed inhibitor of the present invention contains a powder made of an amorphous inorganic material (hereinafter referred to as "amorphous inorganic powder"). The bloom bleed inhibitor of the present invention may be composed only of an amorphous inorganic powder, or may be composed of an amorphous inorganic powder and another powder as long as the occurrence of the bloom bleed phenomenon is suppressed. It may be one.
In the present invention, the term "amorphous" means that a peak detected in an X-ray diffraction image obtained by powder X-ray diffraction measurement is not observed, or even if it is observed, the half-value width of the peak is 0.5 degree or more. It is of low crystalline quality. Figure 1 is a type of amorphous inorganic material, an X-ray diffraction pattern of the powder consisting of 0.01Al 2 O 3 · ZnO · 0.05H 2 O, semi the characteristic diffraction peaks in 31.7degree It is the schematic which shows the method of calculating|requiring price range H, and shows that H is about 0.8 degrees.
上記非晶質無機材料は、特に限定されず、アルカリ金属原子、2価の金属原子、3価の金属原子、及び、4価の金属原子から選ばれる少なくとも一種の金属原子を含む酸化物又はこれを含む複合物であることが好ましく、例えば、下記一般式(1)で表される化合物が好ましい。
aM1 2O・bM2O・cM3 2O3・dM4O2・eP2O5・fH2O (1)
(式中、M1はアルカリ金属原子、M2は2価の金属原子、M3は3価の金属原子、M4は4価の金属原子であり、a、b、c、d及びeのうち、少なくとも1つは正数であり、残りは0又は正数であり、fは正数である。)The amorphous inorganic material is not particularly limited, and an oxide containing at least one metal atom selected from an alkali metal atom, a divalent metal atom, a trivalent metal atom, and a tetravalent metal atom, or an oxide thereof. The compound represented by the following general formula (1) is preferable.
aM 1 2 O·bM 2 O·cM 3 2 O 3 ·dM 4 O 2 ·eP 2 O 5 ·fH 2 O (1)
(In the formula, M 1 is an alkali metal atom, M 2 is a divalent metal atom, M 3 is a trivalent metal atom, M 4 is a tetravalent metal atom, and each of a, b, c, d and e Among them, at least one is a positive number, the rest are 0 or a positive number, and f is a positive number.)
上記一般式(1)において、M1はアルカリ金属原子であり、Li、Na、K、Rb、Cs等が挙げられる。これらのうち、Naが好ましい。M2は2価の金属原子であり、Be、Mg、Ca、Ba等のアルカリ土類金属原子、Cu、Zn、Fe、Co、Ni、Ru、Pd、Pt、Pb、Cd等が挙げられる。これらのうち、Mg及びZnが好ましい。M3は3価の金属原子であり、Al、Fe等が挙げられる。これらのうち、Alが好ましい。また、M4は4価の金属原子であり、Si、Ti、Zr等が挙げられる。これらのうち、Siが好ましい。
尚、上記一般式(1)を構成するM1、M2、M3又はM4は、いずれも一種のみであってよいし、二種以上であってもよい。In the above general formula (1), M 1 is an alkali metal atom, and examples thereof include Li, Na, K, Rb and Cs. Of these, Na is preferred. M 2 is a divalent metal atom, and examples thereof include alkaline earth metal atoms such as Be, Mg, Ca and Ba, Cu, Zn, Fe, Co, Ni, Ru, Pd, Pt, Pb and Cd. Of these, Mg and Zn are preferable. M 3 is a trivalent metal atom, and examples thereof include Al and Fe. Of these, Al is preferable. Further, M 4 is a tetravalent metal atom, and examples thereof include Si, Ti, and Zr. Of these, Si is preferable.
In addition, M 1 , M 2 , M 3 or M 4 constituting the general formula (1) may be only one kind, or may be two or more kinds.
上記一般式(1)で表される化合物の具体例は、下記式(1−1)〜(1−16)で表される。尚、下記式において、a、b、c、d及びeは、0又は正数であり、fは、正数であり、b=b1+b2、c=c1+c2、d=d1+d2である。
aM1 2O・dSiO2・fH2O (1−1)
aM1 2O・bM2O・dSiO2・fH2O (1−2)
aM1 2O・cM3 2O3・dSiO2・fH2O (1−3)
aM1 2O・d1M4O2・d2SiO2・fH2O (1−4)
aM1 2O・bM2O・eP2O5・fH2O (1−5)
aM1 2O・cM3 2O3・eP2O5・fH2O (1−6)
aM1 2O・dM4O2・eP2O5・fH2O (1−7)
aM1 2O・bM2O・cAl2O3・fH2O (1−8)
aM1 2O・c1M3 2O3・c2Al2O3・fH2O (1−9)
aM1 2O・dM4O2・cAl2O3・fH2O (1−10)
aM1 2O・bZnO・fH2O (1−11)
cM3 2O3・bZnO・fH2O (1−12)
aM1 2O・b1M2O・b2ZnO・fH2O (1−13)
aM1 2O・cM3 2O3・bZnO・fH2O (1−14)
aM1 2O・dZrO2・fH2O (1−15)
aM1 2O・dTiO2・fH2O (1−16)Specific examples of the compound represented by the general formula (1) are represented by the following formulas (1-1) to (1-16). In the following formula, a, b, c, d and e are 0 or a positive number, f is a positive number, b=b 1 +b 2 , c=c 1 +c 2 , d=d 1 +d 2 .
aM 1 2 O · dSiO 2 · fH 2 O (1-1)
aM 1 2 O · bM 2 O · dSiO 2 · fH 2 O (1-2)
aM 1 2 O · cM 3 2 O 3 · dSiO 2 · fH 2 O (1-3)
aM 1 2 O · d 1 M 4 O 2 · d 2 SiO 2 · fH 2 O (1-4)
aM 1 2 O · bM 2 O · eP 2 O 5 · fH 2 O (1-5)
aM 1 2 O · cM 3 2 O 3 · eP 2 O 5 · fH 2 O (1-6)
aM 1 2 O · dM 4 O 2 · eP 2 O 5 · fH 2 O (1-7)
aM 1 2 O · bM 2 O · cAl 2 O 3 · fH 2 O (1-8)
aM 1 2 O · c 1 M 3 2 O 3 · c 2 Al 2 O 3 · fH 2 O (1-9)
aM 1 2 O · dM 4 O 2 · cAl 2 O 3 · fH 2 O (1-10)
aM 1 2 O · bZnO · fH 2 O (1-11)
cM 3 2 O 3 .bZnO.fH 2 O (1-12)
aM 1 2 O · b 1 M 2 O · b 2 ZnO · fH 2 O (1-13)
aM 1 2 O · cM 3 2 O 3 · bZnO · fH 2 O (1-14)
aM 1 2 O · dZrO 2 · fH 2 O (1-15)
aM 1 2 O · dTiO 2 · fH 2 O (1-16)
本発明においては、上記一般式(1−1)、(1−2)、(1−3)、(1−11)、(1−12)及び(1−13)で表される化合物が、ブルーム・ブリード現象の発生の抑制効果に優れることから、特に好ましい。具体的な化合物は、以下に例示される。
0.1Na2O・SiO2・0.1H2O
Na2O・0.01MgO・SiO2・0.1H2O
Na2O・0.2Al2O3・SiO2・0.1H2O
0.13Na2O・Al2O3・8.2SiO2・0.7H2O
0.1Na2O・ZnO・0.1H2O
ZnO・0.27H2O
0.2Na2O・0.1MgO・ZnO・0.1H2O
0.007Al2O3・ZnO・0.02H2O
0.007Al2O3・ZnO・0.15H2OIn the present invention, the compounds represented by the general formulas (1-1), (1-2), (1-3), (1-11), (1-12) and (1-13) are It is particularly preferable because it has an excellent effect of suppressing the occurrence of the bloom/bleed phenomenon. Specific compounds are exemplified below.
0.1Na 2 O・SiO 2・0.1H 2 O
Na 2 O/0.01MgO/SiO 2 /0.1H 2 O
Na 2 O/0.2Al 2 O 3 /SiO 2 /0.1H 2 O
0.13Na 2 O・Al 2 O 3・8.2SiO 2・0.7H 2 O
0.1Na 2 O/ZnO/0.1H 2 O
ZnO・0.27H 2 O
0.2Na 2 O/0.1MgO/ZnO/0.1H 2 O
0.007Al 2 O 3 ·ZnO ·0.02H 2 O
0.007Al 2 O 3 ·ZnO ·0.15H 2 O
上記非晶質無機粉末の形状及び粒径は、特に限定されない。レーザー回折式粒度分布機で測定されるメジアン粒径は、好ましくは0.1〜20μm程度である。エラストマー成形品を製造する際に用いる原料組成物における分散性や加工性、並びに、得られるエラストマー成形品におけるブルーム・ブリード現象の発生を抑制する効果が確実に得られることから、特に好ましくは0.5〜15μmである。 The shape and particle size of the amorphous inorganic powder are not particularly limited. The median particle diameter measured by a laser diffraction type particle size distribution machine is preferably about 0.1 to 20 μm. Particularly preferably, the dispersibility and processability of the raw material composition used for producing the elastomer molded product and the effect of suppressing the occurrence of the bloom and bleed phenomenon in the obtained elastomer molded product are reliably obtained. It is 5 to 15 μm.
上記非晶質無機粉末の比表面積は、エラストマー成形品におけるブルーム・ブリード現象の発生を抑制する効果が十分に得られることから、好ましくは30g/m2以上、より好ましくは50m2/g以上、更に好ましくは80m2/g以上、特に好ましくは100〜450m2/gである。尚、上記非晶質無機粉末の比表面積は、BET法で測定することができる。The specific surface area of the amorphous inorganic powder is preferably 30 g/m 2 or more, more preferably 50 m 2 /g or more, since the effect of suppressing the occurrence of the bloom/bleed phenomenon in the elastomer molded product can be sufficiently obtained. more preferably 80 m 2 / g or more, particularly preferably 100~450m 2 / g. The specific surface area of the amorphous inorganic powder can be measured by the BET method.
上記のように、本発明のブルーム・ブリード抑制剤は、他の無機材料又は有機材料からなる粉末(他の粉末)を含有してもよいが、この場合、本発明のブルーム・ブリード抑制剤に含まれる非晶質無機粉末の含有割合の下限は、好ましくは50質量%、より好ましくは80質量%である。 As described above, the bloom bleed inhibitor of the present invention may contain a powder (another powder) made of another inorganic material or an organic material. In this case, the bloom bleed inhibitor of the present invention The lower limit of the content ratio of the amorphous inorganic powder contained is preferably 50% by mass, more preferably 80% by mass.
本発明の組成物(以下、「原料組成物」という)は、上記本発明のブルーム・ブリード抑制剤と、エラストマー又は未架橋ゴムとを含有することを特徴とする。本発明の原料組成物は、更に、樹脂、添加剤、溶剤等を含有することができる。樹脂は、熱可塑性樹脂及び硬化性樹脂のいずれでもよい。以下、樹脂の含有の可否に関わらず、エラストマー又は未架橋ゴムを合わせて「高分子成分」という。 The composition of the present invention (hereinafter referred to as "raw material composition") is characterized by containing the above-described bloom/bleed inhibitor of the present invention and an elastomer or an uncrosslinked rubber. The raw material composition of the present invention may further contain a resin, an additive, a solvent and the like. The resin may be either a thermoplastic resin or a curable resin. Hereinafter, the elastomer or uncrosslinked rubber will be collectively referred to as “polymer component” regardless of whether or not the resin is contained.
上記エラストマー及び未架橋ゴムとしては、ジエン系化合物に由来する構造単位を含む(共)重合体又はその水素添加物(以下、「ジエン系エラストマー」という);オレフィン共重合体;アクリルゴム;ウレタン系エラストマー;ポリエステル系エラストマー;ポリアミド系エラストマー等を用いることができる。 As the elastomer and the uncrosslinked rubber, a (co)polymer containing a structural unit derived from a diene compound or a hydrogenated product thereof (hereinafter referred to as "diene elastomer"); an olefin copolymer; an acrylic rubber; a urethane type Elastomers; polyester elastomers; polyamide elastomers and the like can be used.
上記ジエン系エラストマーは、更に、芳香族ビニル化合物に由来する構造単位、シアン化ビニル化合物に由来する構造単位等を含んでもよい。
上記ジエン系エラストマーとしては、ポリブタジエンゴム、ポリイソプレンゴム、スチレン・ブタジエン共重合ゴム(SBR)、クロロプレンゴム(CR)、アクリロニトリル・ブタジエンゴム(NBR)、イソプレン・イソブチレン共重合ゴム(IIR)、スチレン系AB型ジブロック共重合体、スチレン系ABA型トリブロック共重合体、スチレン系ABAB型テトラブロック共重合体、スチレン系ABABA型ペンタブロック共重合体、これら以上のAB繰り返し単位を有するスチレン系マルチブロック共重合体等が挙げられる。The diene elastomer may further contain a structural unit derived from an aromatic vinyl compound, a structural unit derived from a vinyl cyanide compound, and the like.
Examples of the diene elastomer include polybutadiene rubber, polyisoprene rubber, styrene/butadiene copolymer rubber (SBR), chloroprene rubber (CR), acrylonitrile/butadiene rubber (NBR), isoprene/isobutylene copolymer rubber (IIR), styrene rubber. AB type diblock copolymer, styrene type ABA type triblock copolymer, styrene type ABAB type tetrablock copolymer, styrene type ABABA type pentablock copolymer, styrene type multiblock having AB repeating units of these or more Examples thereof include copolymers.
上記オレフィン共重合体としては、エチレン単位と、α−オレフィンに由来する構造単位とを含み、更に、非共役ジエン化合物に由来する構造単位を含む共重合体又はその無水カルボン酸変性物(以下、「エチレン・α−オレフィン系共重合ゴム」という)、エチレン単位と、不飽和カルボン酸に由来する構造単位とを含む共重合体等が挙げられる。 As the olefin copolymer, an ethylene unit and a structural unit derived from α-olefin, a copolymer containing a structural unit derived from a non-conjugated diene compound or a carboxylic anhydride modified product thereof (hereinafter, "It is referred to as "ethylene/α-olefin copolymer rubber"), a copolymer containing an ethylene unit and a structural unit derived from an unsaturated carboxylic acid, and the like.
上記エチレン・α−オレフィン系共重合ゴムに係るα−オレフィンとしては、プロピレン、1−ブテン、1−ペンテン、1−ヘキセン等が挙げられ、非共役ジエン化合物としては、ジシクロペンタジエン、5−エチリデン−2−ノルボルネン、1,4−ヘキサジエン、メチルテトラヒドロインデン、メチルノルボルネン等が挙げられる。
上記エチレン・α−オレフィン系共重合ゴムとしては、エチレン・プロピレン共重合ゴム、エチレン・ブテン共重合ゴム、エチレン・ヘキセン共重合ゴム、エチレン・オクテン共重合ゴム等が挙げられる。Examples of the α-olefin relating to the ethylene/α-olefin copolymer rubber include propylene, 1-butene, 1-pentene, 1-hexene, and the like, and non-conjugated diene compounds include dicyclopentadiene and 5-ethylidene. 2-norbornene, 1,4-hexadiene, methyltetrahydroindene, methylnorbornene and the like can be mentioned.
Examples of the ethylene/α-olefin copolymer rubber include ethylene/propylene copolymer rubber, ethylene/butene copolymer rubber, ethylene/hexene copolymer rubber, and ethylene/octene copolymer rubber.
上記高分子成分が樹脂を含有する場合、この樹脂は、通常、エラストマー又は未架橋ゴムの種類により、選択される。上記樹脂としては、オレフィン系樹脂、アクリル樹脂、芳香族ビニル化合物に由来する構造単位を含む樹脂等が挙げられる。 When the polymer component contains a resin, the resin is usually selected depending on the type of elastomer or uncrosslinked rubber. Examples of the resin include an olefin resin, an acrylic resin, and a resin containing a structural unit derived from an aromatic vinyl compound.
本発明の原料組成物を製造する場合、均一組成のエラストマー成形体が効率よく得られることから、使用するブルーム・ブリード抑制剤の水分量は、好ましくは1〜15質量%、より好ましくは1〜10質量%である。上記水分量は、カールフィッシャー法により測定することができる。 When the raw material composition of the present invention is produced, an elastomer molded body having a uniform composition can be efficiently obtained. Therefore, the amount of water in the Bloom/bleed inhibitor used is preferably 1 to 15% by mass, more preferably 1 to It is 10% by mass. The water content can be measured by the Karl Fischer method.
本発明の原料組成物におけるブルーム・ブリード抑制剤の含有量は、エラストマー成形品におけるブルーム・ブリード現象の発生を抑制する効果が十分に得られることから、好ましくは0.5〜10質量%、より好ましくは1〜8質量%、更に好ましくは2〜6質量%である。含有量が10質量部を超えると、エラストマー成形品の強度低下、色調変化等の不具合を招く可能性がある。本発明において、ブルーム・ブリード抑制剤は、一種のみ、又は、二種類以上を組み合わせて使用することも可能である。 The content of the bloom bleed inhibitor in the raw material composition of the present invention is preferably 0.5 to 10% by mass, because the effect of suppressing the occurrence of the bloom bleed phenomenon in the elastomer molded product can be sufficiently obtained. It is preferably 1 to 8% by mass, more preferably 2 to 6% by mass. If the content exceeds 10 parts by mass, the elastomer molded product may have problems such as strength reduction and color tone change. In the present invention, the bloom bleed inhibitor may be used alone or in combination of two or more kinds.
本発明の原料組成物は、加工性を向上させる、所望の形状又は特性を有するエラストマー成形品を効率よく製造する等のために、通常、添加剤、溶剤等の配合剤を含有する。
添加剤としては、酸化防止剤、紫外線吸収剤、光安定剤、老化防止剤、可塑剤、難燃剤、帯電防止剤、防黴剤、着色剤、架橋剤(加硫剤)、加硫促進剤、加硫遅延剤、しゃっ解剤、ステアリン酸等の加工助剤、ワックス等の滑剤、プロセスオイル、粘着付与剤、充填剤、メチレン供与体、メチレン受容体有機コバルト化合物等が挙げられる。これらのうち、ブルーム・ブリード現象に係る成分は、酸化防止剤、紫外線吸収剤、光安定剤、老化防止剤、可塑剤、難燃剤、帯電防止剤、防黴剤、加硫促進剤、加工助剤、滑剤、プロセスオイル等である。The raw material composition of the present invention usually contains a compounding agent such as an additive and a solvent in order to improve processability and efficiently produce an elastomer molded article having a desired shape or characteristic.
As additives, antioxidants, ultraviolet absorbers, light stabilizers, antioxidants, plasticizers, flame retardants, antistatic agents, mildew-proofing agents, colorants, cross-linking agents (vulcanizing agents), vulcanization accelerators. , A vulcanization retarder, a pacifier, a processing aid such as stearic acid, a lubricant such as wax, a process oil, a tackifier, a filler, a methylene donor, and a methylene acceptor organic cobalt compound. Among these, components related to the bloom/bleed phenomenon are antioxidants, ultraviolet absorbers, light stabilizers, antiaging agents, plasticizers, flame retardants, antistatic agents, antifungal agents, vulcanization accelerators, processing aids. Agents, lubricants, process oils, etc.
上記酸化防止剤としては、ヒンダードアミン系化合物、ハイドロキノン系化合物、ヒンダードフェノール系化合物、含硫黄化合物、含リン化合物等が挙げられる。
上記紫外線吸収剤としては、ベンゾフェノン系化合物、ベンゾトリアゾール系化合物、
トリアジン系化合物等が挙げられる。
上記光安定剤としては、ヒンダードアミン系化合物等が挙げられる。
上記老化防止剤としては、ナフチルアミン系化合物、ジフェニルアミン系化合物、p−フェニレンジアミン系化合物、キノリン系化合物、ヒドロキノン誘導体系化合物、モノフェノール系化合物、ビスフェノール系化合物、トリスフェノール系化合物、ポリフェノール系化合物、チオビスフェノール系化合物、ヒンダードフェノール系化合物、亜リン酸エステル系化合物、イミダゾール系化合物、ジチオカルバミン酸ニッケル塩系化合物、リン酸系化合物等が挙げられる。Examples of the antioxidant include hindered amine compounds, hydroquinone compounds, hindered phenol compounds, sulfur-containing compounds, phosphorus-containing compounds and the like.
As the ultraviolet absorber, a benzophenone compound, a benzotriazole compound,
Examples thereof include triazine-based compounds.
Examples of the light stabilizer include hindered amine compounds.
Examples of the antioxidant include naphthylamine compounds, diphenylamine compounds, p-phenylenediamine compounds, quinoline compounds, hydroquinone derivative compounds, monophenol compounds, bisphenol compounds, trisphenol compounds, polyphenol compounds, thiol. Examples thereof include bisphenol type compounds, hindered phenol type compounds, phosphite type compounds, imidazole type compounds, dithiocarbamic acid nickel salt type compounds and phosphoric acid type compounds.
上記可塑剤としては、フタル酸エステル、トリメリット酸エステル、ピロメリット酸エステル、脂肪族一塩基酸エステル、脂肪族二塩基酸エステル、リン酸エステル、多価アルコールのエステル、エポキシ系可塑剤、高分子型可塑剤、塩素化パラフィン等が挙げられる。
上記難燃剤としては、含ハロゲン化合物、含リン化合物、シリコーン系化合物等が挙げられる。
上記加硫促進剤としては、ジメチルジチオカルバミン酸亜鉛、ジエチルチオカルバミン酸亜鉛、ジ−n−ブチルジチオカルバミン酸亜鉛、エチルフェニルジチオカルバミン酸亜鉛、ブチルフェニルジチオカルバミン酸亜鉛、ジメチルジチオカルバミン酸ナトリウム、ジメチルジチオカルバミン酸セレン、ジエチルジチオカルバミン酸テルル等のジチオカルバミン酸系化合物;テトラメチルチウラムモノスルフィド、テトラメチルチウラムジスルフィド、テトラエチルウラムジスルフィド、テトラブチルチウラムジスルフィド、ジペンタメチレンチウラムテトラスルフィド等のチウラム系化合物;N−シクロヘキシル−2−ベンゾチアゾールスルフェンアミド、N−オキシジエチレン−2−ベンゾチアゾールスルフェンアミド、N,N−ジイソプロピル−2−ベンゾチアゾールスルフェンアミド、2−メルカプロベンゾチアゾール、2−(2,4−ジニトロフェニル)メルカプトベンゾチアゾール、2−(2,6−ジエチル−4−モルホリノチオ)ベンゾチアゾール、ジベンゾチアゾール−ジベンゾチアジル−ジスルフィド等のチアゾール系化合物;ジフェニルグアニジン、トリフェニルグアニジン、ジオルソトリルグアニジン、オルソトリル−ビ−グアニド、ジフェニルグアニジンフタレート等のグアニジン系化合物;チオカルバニリド、ジエチルチオウレア、ジブチルチオウレア、トリメチルチオウレア、ジオルソトリルチオウレア等のチオウレア系化合物;アセトアルデヒド−アニリン縮合物、ヘキサメチレンテトラミン、アセトアルデヒドアンモニア等のアルデヒドアミン又はアルデヒド−アンモニア系化合物;2−メルカプトイミダゾリン等のイミダゾリン系化合物;ジブチルキサントゲン酸亜鉛等のザンテート系化合物;亜鉛華等が挙げられる。
上記プロセスオイルとしては、ナフテン系オイル、パラフィン系オイル等が挙げられる。Examples of the plasticizer include phthalic acid ester, trimellitic acid ester, pyromellitic acid ester, aliphatic monobasic acid ester, aliphatic dibasic acid ester, phosphoric acid ester, polyhydric alcohol ester, epoxy plasticizer, high Examples include molecular type plasticizers and chlorinated paraffins.
Examples of the flame retardant include halogen-containing compounds, phosphorus-containing compounds and silicone compounds.
Examples of the vulcanization accelerator include zinc dimethyldithiocarbamate, zinc diethylthiocarbamate, zinc di-n-butyldithiocarbamate, zinc ethylphenyldithiocarbamate, zinc butylphenyldithiocarbamate, sodium dimethyldithiocarbamate, selenium dimethyldithiocarbamate, Dithiocarbamate compounds such as tellurium diethyldithiocarbamate; Thiuram compounds such as tetramethylthiuram monosulfide, tetramethylthiuram disulfide, tetraethyluram disulfide, tetrabutylthiuram disulfide, dipentamethylenethiuram tetrasulfide; N-cyclohexyl-2-benzo Thiazolesulfenamide, N-oxydiethylene-2-benzothiazolesulfenamide, N,N-diisopropyl-2-benzothiazolesulfenamide, 2-mercaprobenzothiazole, 2-(2,4-dinitrophenyl)mercapto Thiazole compounds such as benzothiazole, 2-(2,6-diethyl-4-morpholinothio)benzothiazole, dibenzothiazole-dibenzothiazyl-disulfide; diphenylguanidine, triphenylguanidine, diorthotrilguanidine, orthotril-bi- Guanidine compounds such as guanide and diphenylguanidine phthalate; thiourea compounds such as thiocarbanilide, diethylthiourea, dibutylthiourea, trimethylthiourea, diorsotolylthiourea; aldehyde amines or aldehydes such as acetaldehyde-aniline condensates, hexamethylenetetramine, acetaldehyde ammonia. -Ammonia-based compounds; imidazoline-based compounds such as 2-mercaptoimidazoline; xanthate-based compounds such as zinc dibutylxanthate; zinc white and the like.
Examples of the process oil include naphthenic oil and paraffinic oil.
上記充填剤としては、シリカ、タルク、炭酸カルシウム、カーボンブラック等の無機充填剤;クマロンインデン樹脂、ハイスチレン樹脂、フェノール樹脂等の高分子充填剤が挙げられる。 Examples of the filler include inorganic fillers such as silica, talc, calcium carbonate and carbon black; polymer fillers such as coumarone indene resin, high styrene resin and phenol resin.
架橋構造を有するエラストマー成形品を製造する場合には、イオウ系化合物、有機過酸化物等の架橋剤(加硫剤)が用いられる。
上記イオウ系化合物としては、イオウ、塩化イオウ、二塩化イオウ、モルホリンジスルフィド、アルキルフェノールジスルフィド、テトラメチルチウラムジスルフィド、ジメチルジチオカルバミン酸セレン等が挙げられる。
上記有機過酸化物としては、ジクミルペルオキシド、2,5−ジメチル−2,5−ジ(tert−ブチルペルオキシ)ヘキサン、2,5−ジメチル−2,5−ジ(ベンゾイルペルオキシ)ヘキサン、2,5−ジメチル−2,5−ジ(tert−ブチルペルオキシ)ヘキシン−3、ジ−tert−ブチルペルオキシド、ジ−tert−ブチルペルオキシ−3,3,5−トリメチルシクロヘキサン、tert−ブチルヒドロペルオキシド等が挙げられる。When producing an elastomer molded article having a crosslinked structure, a crosslinking agent (vulcanizing agent) such as a sulfur compound or an organic peroxide is used.
Examples of the sulfur compounds include sulfur, sulfur chloride, sulfur dichloride, morpholine disulfide, alkylphenol disulfide, tetramethylthiuram disulfide, and selenium dimethyldithiocarbamate.
As the organic peroxide, dicumyl peroxide, 2,5-dimethyl-2,5-di(tert-butylperoxy)hexane, 2,5-dimethyl-2,5-di(benzoylperoxy)hexane, 2, 5-dimethyl-2,5-di(tert-butylperoxy)hexyne-3, di-tert-butylperoxide, di-tert-butylperoxy-3,3,5-trimethylcyclohexane, tert-butylhydroperoxide and the like can be mentioned. To be
尚、架橋剤として有機過酸化物を使用する場合、架橋助剤と併用することが好ましい。架橋助剤としては、イオウ;p−キノンジオキシム等のキノンジオキシム系化合物;ポリエチレングリコールジメタクリレート等のメタクリレート系化合物;ジアリルフタレート、トリアリルシアヌレート等のアリル系化合物;ビスマレイミド等のマレイミド系化合物;ジビニルベンゼン等が挙げられる。
また、加硫剤としてイオウ系化合物を使用する場合、上記加硫促進剤と併用することが好ましい。When an organic peroxide is used as the cross-linking agent, it is preferably used together with a cross-linking aid. As the cross-linking aid, sulfur; quinone dioxime compounds such as p-quinone dioxime; methacrylate compounds such as polyethylene glycol dimethacrylate; allyl compounds such as diallyl phthalate and triallyl cyanurate; maleimide compounds such as bismaleimide. Compounds: divinylbenzene and the like can be mentioned.
When a sulfur compound is used as the vulcanizing agent, it is preferably used in combination with the vulcanization accelerator.
本発明の原料組成物は、例えば、原料成分を、密閉型混練機、オーブンロール、押出機等により、混練した後、得られた混練物に、必要に応じて、架橋剤(加硫剤)、加硫促進剤等を配合することにより製造することができる。ここで、原料成分の使用方法としては、全量を一括して用いる方法、ブルーム・ブリード抑制剤と配合剤とを、予め混合し、その後、得られた混合物と、エラストマー又は未架橋ゴムとを混練する方法等とすることができる。 The raw material composition of the present invention, for example, after the raw material components are kneaded by a closed kneading machine, an oven roll, an extruder, etc., the resulting kneaded product, if necessary, a crosslinking agent (vulcanizing agent) It can be produced by adding a vulcanization accelerator or the like. Here, as a method of using the raw material components, a method of using the whole amount at once, a Bloom bleed inhibitor and a compounding agent are mixed in advance, and then the obtained mixture is kneaded with an elastomer or an uncrosslinked rubber. It can be set as a method or the like.
本発明のエラストマー成形品は、上記本発明の原料組成物を用いて得られた物品である。具体的な製造方法は、射出成型、押出成型、インフレーション成型、真空成型、発泡成型、熱プレス等が挙げられる。従って、本発明のエラストマー成形品は、中実体又は発泡体からなるものとすることができ、固体部分においては、架橋された高分子マトリックス又は非架橋の高分子マトリックスの中に、ブルーム・ブリード抑制剤と、原料組成物に配合剤として含まれたブルーム・ブリード現象に係る成分とが分散して含まれた構造を有する。 The elastomer molded article of the present invention is an article obtained by using the above-mentioned raw material composition of the present invention. Specific manufacturing methods include injection molding, extrusion molding, inflation molding, vacuum molding, foam molding, and heat pressing. Therefore, the elastomer molded article of the present invention can be composed of a solid body or a foam, and in the solid portion, it is possible to suppress bloom bleed in a crosslinked polymer matrix or an uncrosslinked polymer matrix. It has a structure in which an agent and a component relating to the bloom bleed phenomenon included as a compounding agent in the raw material composition are dispersed and included.
本発明のブルーム・ブリード抑制剤を含むエラストマー成形品が、ブルーム・ブリード現象の発生が抑制される効果を有する理由は、判明していないが、本発明者は、ブルーム・ブリード抑制剤と添加剤との親和性が高いことによるものと考えている。 The reason why the elastomer molded article containing the bloom bleed inhibitor of the present invention has the effect of suppressing the occurrence of the bloom bleed phenomenon is not known, but the present inventors have found that the bloom bleed inhibitor and the additive We believe that this is due to its high affinity with.
以下、実施例を挙げて、本発明を更に具体的に説明するが、本発明は、かかる実施例に限定されるものではない。尚、「%」は質量%である。 Hereinafter, the present invention will be described in more detail with reference to examples, but the present invention is not limited to the examples. In addition, "%" is the mass %.
1.評価方法
(1)ブルーム・ブリード抑制剤の粉末X線回折
粉末X線回折の測定を、リガク社製X線回折装置「RINT2400V」(型式名)を用いて、Cu Kα線により行い、X線回折像を得た。測定条件は、管電圧40kV及び電流150mAとした。得られた回折ピークの特定位置(2θ)における半値幅を、図1に示す方法により求めた。
(2)ブルーム・ブリード抑制剤の比表面積
JIS Z8830−2001、「気体吸着による粉体(固体)の比表面積測定方法」に準じ、堀場製作所社製連続流動式表面積計「SA−6200」(型式名)を用いて測定した。
(3)ブルーム・ブリード抑制剤のメジアン粒径(d50)
ブルーム・ブリード抑制剤を、マルバーン社製レーザー回折式粒度分布測定装置「MS2000」(型式名)を用いて測定し、メジアン粒径(d50)を体積基準で測定した。
(4)ブルーム・ブリード現象の抑制効果確認試験
70質量部のスチレン系テトラブロック共重合体の水素添加物と、30質量部のスチレン系トリブロック共重合体の水素添加物と、20質量部のポリプロピレン樹脂と、これらの高分子成分の合計に対して、3質量%又は6質量%相当量のブルーム・ブリード抑制剤と、0.5質量部のカーボンブラックとを、ヘンシェルミキサーを用いてドライブレンドした。次いで、100質量部のナフテン系オイルを添加して、十分に混合し原料組成物を得た。その後、押出機を用いて約200℃で溶融混練して、原料ペレットを作製した。そして、射出成形機を用い、170℃で板状試験片(11mm×11mm×1mm)を得た。そして、50℃で2週間保管した。保管前後の板状試験片の表面を目視観察し、下記基準で評価した。
○:ブリード又は虹色発色現象等が見られなかった
×:ブリード又は虹色発色現象が顕著であった1. Evaluation Method (1) Powder X-Ray Diffraction of Bloom Bleed Inhibitor Powder X-ray diffraction was measured by Cu Kα ray using Rigaku X-ray diffractometer "RINT2400V" (model name), and X-ray diffraction was performed. Got the statue. The measurement conditions were a tube voltage of 40 kV and a current of 150 mA. The full width at half maximum of the obtained diffraction peak at the specific position (2θ) was determined by the method shown in FIG.
(2) Specific Surface Area of Bloom/Bleed Inhibitor According to JIS Z8830-2001, “Method for measuring specific surface area of powder (solid) by gas adsorption”, continuous flow type surface area meter “SA-6200” manufactured by Horiba Ltd. Name).
(3) Median particle size (d50) of the bloom/bleed inhibitor
The bloom bleed inhibitor was measured using a laser diffraction particle size distribution analyzer “MS2000” (model name) manufactured by Malvern Instruments Ltd., and the median particle diameter (d50) was measured on a volume basis.
(4) Test for confirming effect of suppressing bloom/bleed phenomenon 70 parts by mass of styrene-based tetrablock copolymer hydrogenated product, 30 parts by mass of styrene-based triblock copolymer hydrogenated product, and 20 parts by mass of Dry blend of polypropylene resin, 3 mass% or 6 mass% equivalent bloom/bleed inhibitor, and 0.5 mass part of carbon black with respect to the total of these polymer components using a Henschel mixer. did. Next, 100 parts by mass of naphthenic oil was added and mixed sufficiently to obtain a raw material composition. Then, the raw material pellet was produced by melt-kneading at about 200° C. using an extruder. Then, using an injection molding machine, a plate-shaped test piece (11 mm×11 mm×1 mm) was obtained at 170° C. Then, it was stored at 50° C. for 2 weeks. The surface of the plate-shaped test piece before and after storage was visually observed and evaluated according to the following criteria.
◯: No bleeding or iridescent coloring phenomenon was observed ×: Bleeding or iridescent coloring phenomenon was remarkable
2.ブルーム・ブリード抑制剤を含有する組成物の調製、試験片(エラストマー成形品)の作製及び評価
実施例1及び2
ブルーム・ブリード抑制剤として、X線回折像の31.7deg.における回折ピークの半値幅が約0.8deg.である0.007Al2O3・ZnO・0.15H2O粉末(比表面積:104m2/g、メジアン粒径:1.7μm)を用い、高分子成分の合計に対してこれを3質量%又は6質量%含む原料組成物を調製した。その後、ブルーム・ブリード現象の抑制効果確認試験を行った(表1参照)。2. Preparation of Composition Containing Bloom/Bleed Inhibitor, Preparation and Evaluation of Test Piece (Elastomer Molded Article) Examples 1 and 2
As a bloom bleed inhibitor, 31.7 deg. The half-value width of the diffraction peak at about 0.8 deg. 0.007Al 2 O 3 .ZnO.0.15H 2 O powder (specific surface area: 104 m 2 /g, median particle size: 1.7 μm) was used, and this was 3% by mass with respect to the total of the polymer components. Alternatively, a raw material composition containing 6% by mass was prepared. Then, a test for confirming the effect of suppressing the bloom/bleed phenomenon was conducted (see Table 1).
実施例3
ブルーム・ブリード抑制剤として、X線回折像で明瞭な回折ピークが検出されないZnO・0.27H2O粉末(比表面積:188m2/g、メジアン粒径:9.8μm)を用い、高分子成分の合計に対してこれを3質量%含む原料組成物を調製した。その後、ブルーム・ブリード現象の抑制効果確認試験を行った(表1参照)。Example 3
As a bloom/bleed suppressor, ZnO.0.27H 2 O powder (specific surface area: 188 m 2 /g, median particle size: 9.8 μm) in which a clear diffraction peak was not detected in an X-ray diffraction image was used. A raw material composition containing 3 mass% of this was prepared. Then, a test for confirming the effect of suppressing the bloom/bleed phenomenon was conducted (see Table 1).
実施例4
ブルーム・ブリード抑制剤として、X線回折像で明瞭な回折ピークが検出されない0.13Na2O・Al2O3・8.2SiO2・0.7H2O粉末(比表面積:245m2/g、メジアン粒径:7.9μm)を用い、高分子成分の合計に対してこれを3質量%含む原料組成物を調製した。その後、ブルーム・ブリード現象の抑制効果確認試験を行った(表1参照)。Example 4
As Bloom bleed inhibitor, 0.13Na to clear diffraction peak in X-ray diffraction pattern is not detected 2 O · Al 2 O 3 · 8.2SiO 2 · 0.7H 2 O powder (specific surface area: 245m 2 / g, Using a median particle diameter of 7.9 μm), a raw material composition containing 3% by mass of the polymer component was prepared. Then, a test for confirming the effect of suppressing the bloom/bleed phenomenon was conducted (see Table 1).
比較例1
ブルーム・ブリード抑制剤として、X線回折像の31.7deg.における回折ピークの半値幅が0.1deg.である酸化亜鉛(以下、「酸化亜鉛(I)」という)からなる粉末(比表面積:0.4m2/g、メジアン粒径:0.3μm)を用い、高分子成分の合計に対してこれを3質量%含む原料組成物を調製した。その後、ブルーム・ブリード現象の抑制効果確認試験を行った(表1参照)。Comparative Example 1
As a bloom bleed inhibitor, 31.7 deg. The half-value width of the diffraction peak at 0.1 deg. A powder (specific surface area: 0.4 m 2 /g, median particle size: 0.3 μm) made of zinc oxide (hereinafter, referred to as “zinc oxide (I)”) is used for the total amount of polymer components. A raw material composition containing 3% by mass was prepared. Then, a test for confirming the effect of suppressing the bloom/bleed phenomenon was conducted (see Table 1).
比較例2
ブルーム・ブリード抑制剤として、X線回折像の31.7deg.における回折ピークの半値幅が0.3deg.である酸化亜鉛(以下、「酸化亜鉛(II)」という)からなる粉末(比表面積:20m2/g、メジアン粒径:0.2μm)を用い、高分子成分の合計に対してこれを3質量%含む原料組成物を調製した。その後、ブルーム・ブリード現象の抑制効果確認試験を行った(表1参照)。Comparative example 2
As a bloom bleed inhibitor, 31.7 deg. The half width of the diffraction peak at 0.3 deg. A powder (specific surface area: 20 m 2 /g, median particle diameter: 0.2 μm) made of zinc oxide (hereinafter, referred to as “zinc oxide (II)”) was used, and this was 3 A raw material composition containing mass% was prepared. Then, a test for confirming the effect of suppressing the bloom/bleed phenomenon was conducted (see Table 1).
比較例3
ブルーム・ブリード抑制剤として、X線回折像の9.4deg.における回折ピークの半値幅が0.2deg.であるタルク粉末(比表面積:22m2/g、メジアン粒径:7.8μm)を用い、高分子成分の合計に対してこれを3質量%含む原料組成物を調製した。その後、ブルーム・ブリード現象の抑制効果確認試験を行った(表1参照)。Comparative Example 3
As a bloom bleed inhibitor, an X-ray diffraction image of 9.4 deg. Half width of the diffraction peak at 0.2 deg. Of talc powder (specific surface area: 22 m 2 /g, median particle size: 7.8 μm) was used to prepare a raw material composition containing 3% by mass of the total amount of polymer components. Then, a test for confirming the effect of suppressing the bloom/bleed phenomenon was conducted (see Table 1).
比較例4
ブルーム・ブリード抑制剤を配合しないエラストマーのみを用いて、板状試験片を作製し、ブルーム・ブリード現象の抑制効果確認試験を行った(表1参照)。Comparative Example 4
A plate-shaped test piece was prepared using only an elastomer containing no bloom/bleed inhibitor, and a test for confirming the bloom/bleed phenomenon suppression effect was conducted (see Table 1).
表1から明らかなように、実施例1〜4で用いたブルーム・ブリード抑制剤は、長期に渡って、ブルーム・ブリード現象の抑制効果を有するエラストマー成形品を与えることが分かる。 As is clear from Table 1, the bloom bleed inhibitors used in Examples 1 to 4 provide elastomer molded products having a bloom bleed phenomenon suppression effect over a long period of time.
本発明のブルーム・ブリード抑制剤又はこれを含む組成物を使用することで、各種エラストマー成形品の外観不良等の不具合が抑制されるので、物性の低下等を低減することができる。従って、本発明のブルーム・ブリード抑制剤又はこれを含む組成物は、長期に渡って使用される、車両分野、OA・家電分野、電気・電子分野、医療分野、工具、日用雑貨等の各種部材の形成に好適である。そして、具体的なエラストマー成形品としては、ガスケット、キャップシール、チューブ、消音ギア、工具類のグリップ、歯ブラシ、ペン、かみそり、カッター等のグリップ、靴底、ハンドブレーキグリップカバー、シフトノブ、アームレスト、アシストグリップ、玩具等が挙げられる。 By using the bloom/bleed inhibitor of the present invention or the composition containing the same, problems such as poor appearance of various elastomer molded products can be suppressed, and thus deterioration of physical properties and the like can be suppressed. Therefore, the bloom bleed inhibitor of the present invention or the composition containing the same is used for a long period of time in various fields such as vehicle field, OA/home appliances field, electric/electronic field, medical field, tools, daily sundries and the like. It is suitable for forming members. Specific examples of elastomer molded products include gaskets, cap seals, tubes, noise reduction gears, grips for tools, toothbrushes, pens, razors, grips for cutters, shoe soles, handbrake grip covers, shift knobs, armrests, assists. Examples include grips and toys.
Claims (5)
aNa 2 O・bZnO・cAl 2 O 3 ・dSiO 2 ・fH 2 O (1)
(式中、a、b、c、dは0又は正数であり、かつ、b及びcのうち、少なくとも1つは正数であり、fは正数である。) From an elastomer molded article containing an elastomer containing a hydrogenated product of a copolymer containing a structural unit derived from a diene compound and a structural unit derived from an aromatic vinyl compound, and a compounding agent containing a naphthenic oil , A material for suppressing bleeding or bloom of a compounding agent, which contains a powder of an inorganic material, wherein the inorganic material is a compound represented by the following general formula (1), and by powder X-ray diffraction measurement: A bloom bleed inhibitor having a low crystallinity in which the peak detected in the obtained X-ray diffraction image is not observed, or even if it is observed, the half-width of the peak is 0.5 degree or more.
aNa 2 O·bZnO·cAl 2 O 3 ·dSiO 2 · fH 2 O (1)
(In the formula, a, b, c, d are 0 or a positive number, and at least one of b and c is a positive number and f is a positive number.)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2016089873 | 2016-04-27 | ||
JP2016089873 | 2016-04-27 | ||
PCT/JP2017/006033 WO2017187727A1 (en) | 2016-04-27 | 2017-02-20 | Blooming/bleeding-preventing agent and composition containing same, and elastomer molded article |
Publications (2)
Publication Number | Publication Date |
---|---|
JPWO2017187727A1 JPWO2017187727A1 (en) | 2019-02-28 |
JP6750673B2 true JP6750673B2 (en) | 2020-09-02 |
Family
ID=60160262
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2018514142A Expired - Fee Related JP6750673B2 (en) | 2016-04-27 | 2017-02-20 | Bloom bleed inhibitor, composition containing the same, and elastomer molded article |
Country Status (5)
Country | Link |
---|---|
JP (1) | JP6750673B2 (en) |
KR (1) | KR20190003509A (en) |
CN (1) | CN108884278B (en) |
TW (1) | TWI729077B (en) |
WO (1) | WO2017187727A1 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019167745A1 (en) * | 2018-02-27 | 2019-09-06 | 日本ゼオン株式会社 | Tetra-block copolymer, and polymer composition, and hot-melt sticky adhesive composition using these |
CN111574757B (en) * | 2020-05-28 | 2022-05-13 | 厦门正新橡胶工业有限公司 | Rapid assessment method for rapid blooming of protective wax |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3610301B2 (en) * | 2000-12-06 | 2005-01-12 | 株式会社タイキ | Fine resin particles for makeup |
JP4804651B2 (en) * | 2001-06-13 | 2011-11-02 | 日本化学工業株式会社 | Red phosphorus flame retardant composition for epoxy resin, production method thereof, epoxy resin composition for semiconductor encapsulant, encapsulant, and semiconductor device |
JP4619628B2 (en) * | 2003-04-24 | 2011-01-26 | 株式会社イノアックコーポレーション | Conductive resin composition and method for producing the same |
JP5048395B2 (en) * | 2007-06-05 | 2012-10-17 | 日本ペイント株式会社 | Inorganic organic composite coating composition |
JP5929317B2 (en) * | 2012-02-29 | 2016-06-01 | 大日本印刷株式会社 | Sealant film and packaging material using the same |
CN105518180B (en) * | 2013-09-05 | 2019-02-05 | 三菱工程塑料株式会社 | Thermoplastic resin composition, synthetic resin and the synthetic resin with plating layer manufacturing method |
JP6324059B2 (en) * | 2013-12-24 | 2018-05-16 | 日本合成化学工業株式会社 | Resin composition, coat layer, heat-sensitive recording medium, and aqueous coating solution |
WO2015194466A1 (en) * | 2014-06-17 | 2015-12-23 | 石原産業株式会社 | Titanium dioxide pigment and method for manufacturing same, and composition in which same is blended |
-
2017
- 2017-02-20 WO PCT/JP2017/006033 patent/WO2017187727A1/en active Application Filing
- 2017-02-20 KR KR1020187030581A patent/KR20190003509A/en not_active Application Discontinuation
- 2017-02-20 CN CN201780019807.1A patent/CN108884278B/en not_active Expired - Fee Related
- 2017-02-20 JP JP2018514142A patent/JP6750673B2/en not_active Expired - Fee Related
- 2017-02-22 TW TW106105954A patent/TWI729077B/en active
Also Published As
Publication number | Publication date |
---|---|
TWI729077B (en) | 2021-06-01 |
CN108884278A (en) | 2018-11-23 |
TW201825572A (en) | 2018-07-16 |
WO2017187727A1 (en) | 2017-11-02 |
KR20190003509A (en) | 2019-01-09 |
JPWO2017187727A1 (en) | 2019-02-28 |
CN108884278B (en) | 2021-04-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR101572776B1 (en) | Foam composition, method for producing same, and foam | |
JP6336630B2 (en) | Thermoplastic elastomer composition having improved vibration insulation and heat resistance and molded article formed therefrom | |
JP6609650B2 (en) | Thermoplastic elastomer composition for crosslinked foam and use thereof | |
JP6071175B2 (en) | Thermoplastic elastomer composition | |
JP2006002085A (en) | Thermoplastic elastomer composition | |
JP6750673B2 (en) | Bloom bleed inhibitor, composition containing the same, and elastomer molded article | |
JP4050570B2 (en) | Flame retardant thermoplastic elastomer composition | |
KR102272775B1 (en) | Thermoplastic elastomer composition with excellent molding appearance and molded article thereof | |
JP2021172812A (en) | Thermoplastic elastomer composition and molded body | |
JP2001059049A (en) | Thermoplastic elastomer composition | |
JP2008226850A (en) | Flame-retardant thermoplastic elastomer resin composition and manufacturing method therefor | |
JP6512054B2 (en) | Method for producing resin composition | |
JP2013028653A (en) | Thermoplastic elastomer composition | |
JP2005036169A (en) | Thermoplastic elastomer composition | |
KR102387508B1 (en) | Polymer compositions and uses thereof | |
JP2000327846A (en) | Thermoplastic elastomer composition | |
JP2017075236A (en) | Rubber composition and pneumatic tire prepared therewith | |
JP2004075874A (en) | Conveyor roller | |
JP2010272531A (en) | Flame-retardant thermoplastic elastomer resin composition and method for manufacturing the same | |
JP2002348434A (en) | Thermoplastic elastomer composition | |
KR101501688B1 (en) | Thermoplastic elastomer composition and molded article manufactured therefrom having advenced thermal resistance | |
WO2002051929A1 (en) | Thermoplastic elastomer composition | |
JP2004307564A (en) | Styrenic thermoplastic elastomer composition | |
JP2009013429A (en) | Thermoplastic elastomer composition | |
JP2020122039A (en) | Fire-retardant ethylene copolymer composition and railway product |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20181024 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20190904 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20191029 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20191217 |
|
RD02 | Notification of acceptance of power of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7422 Effective date: 20191217 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20200407 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20200525 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20200714 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20200727 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 6750673 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
LAPS | Cancellation because of no payment of annual fees |