JP2012507548A5 - - Google Patents

Info

Publication number

JP2012507548A5

JP2012507548A5 JP2011534751A JP2011534751A JP2012507548A5 JP 2012507548 A5 JP2012507548 A5 JP 2012507548A5 JP 2011534751 A JP2011534751 A JP 2011534751A JP 2011534751 A JP2011534751 A JP 2011534751A JP 2012507548 A5 JP2012507548 A5 JP 2012507548A5

Authority

JP

Japan

Prior art keywords

ethyl

toluene

ester

bis

acid

Prior art date

2009-10-29

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Granted

Links

• Espacenet
• Global Dossier
• Discuss

• -1 2-ethylhexyl Chemical group 0.000 claims description 58
• 239000002253 acid Substances 0.000 claims description 45
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 24
• 229910052717 sulfur Inorganic materials 0.000 claims description 24
• 239000011593 sulfur Substances 0.000 claims description 24
• 239000000203 mixture Substances 0.000 claims description 17
• 150000001334 alicyclic compounds Chemical class 0.000 claims description 12
• FHBSGPWHCCIQPG-UHFFFAOYSA-N hydroxy-methyl-oxo-sulfanylidene-$l^{6}-sulfane Chemical compound CS(S)(=O)=O FHBSGPWHCCIQPG-UHFFFAOYSA-N 0.000 claims description 12
• 150000002148 esters Chemical class 0.000 claims description 5
• YOZTUWQIMBMYPN-UHFFFAOYSA-N 2-[4,6-bis[2-(benzenesulfonylsulfanyl)ethyl]-2,4,6-trimethyl-1,3,5,2,4,6-trioxatrisilinan-2-yl]ethoxy-oxo-phenyl-sulfanylidene-$l^{6}-sulfane Chemical compound O1[Si](C)(CCSS(=O)(=O)C=2C=CC=CC=2)O[Si](C)(CCSS(=O)(=O)C=2C=CC=CC=2)O[Si]1(C)CCOS(=O)(=S)C1=CC=CC=C1 YOZTUWQIMBMYPN-UHFFFAOYSA-N 0.000 claims description 3
• IKPAUUCODANWTA-UHFFFAOYSA-N cyclohexyl-hydroxy-oxo-sulfanylidene-$l^{6}-sulfane Chemical compound SS(=O)(=O)C1CCCCC1 IKPAUUCODANWTA-UHFFFAOYSA-N 0.000 claims description 3
• AKCUHGBLDXXTOM-UHFFFAOYSA-N hydroxy-oxo-phenyl-sulfanylidene-$l^{6}-sulfane Chemical compound SS(=O)(=O)C1=CC=CC=C1 AKCUHGBLDXXTOM-UHFFFAOYSA-N 0.000 claims description 3
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
• 229920001971 elastomer Polymers 0.000 claims 19
• 239000000806 elastomer Substances 0.000 claims 12
• PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 8
• 239000000945 filler Substances 0.000 claims 7
• 239000005060 rubber Substances 0.000 claims 7
• BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims 6
• 229910000077 silane Inorganic materials 0.000 claims 6
• RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 claims 4
• 229920002857 polybutadiene Polymers 0.000 claims 4
• RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims 3
• MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims 3
• 125000004432 carbon atom Chemical group C* 0.000 claims 3
• 238000007720 emulsion polymerization reaction Methods 0.000 claims 3
• KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims 2
• 239000004215 Carbon black (E152) Substances 0.000 claims 2
• XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims 2
• 239000005062 Polybutadiene Substances 0.000 claims 2
• VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 2
• 229910052783 alkali metal Inorganic materials 0.000 claims 2
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
• 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
• 239000003795 chemical substances by application Substances 0.000 claims 2
• 229910052801 chlorine Inorganic materials 0.000 claims 2
• 239000000460 chlorine Substances 0.000 claims 2
• 229920001577 copolymer Polymers 0.000 claims 2
• 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 2
• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 2
• 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 2
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
• 150000004820 halides Chemical class 0.000 claims 2
• DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 claims 2
• 229930195733 hydrocarbon Natural products 0.000 claims 2
• 150000002430 hydrocarbons Chemical class 0.000 claims 2
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
• VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims 2
• 125000006178 methyl benzyl group Chemical group 0.000 claims 2
• 125000002950 monocyclic group Chemical group 0.000 claims 2
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
• 229920001021 polysulfide Polymers 0.000 claims 2
• 239000005077 polysulfide Substances 0.000 claims 2
• 150000008117 polysulfides Polymers 0.000 claims 2
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
• 229920001897 terpolymer Polymers 0.000 claims 2
• 125000003944 tolyl group Chemical group 0.000 claims 2
• 125000005023 xylyl group Chemical group 0.000 claims 2
• NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims 1
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
• 239000005065 High vinyl polybutadiene Substances 0.000 claims 1
• 125000001931 aliphatic group Chemical group 0.000 claims 1
• RTACIUYXLGWTAE-UHFFFAOYSA-N buta-1,3-diene;2-methylbuta-1,3-diene;styrene Chemical compound C=CC=C.CC(=C)C=C.C=CC1=CC=CC=C1 RTACIUYXLGWTAE-UHFFFAOYSA-N 0.000 claims 1
• 229910052799 carbon Inorganic materials 0.000 claims 1
• 125000001309 chloro group Chemical group Cl* 0.000 claims 1
• 229920003193 cis-1,4-polybutadiene polymer Polymers 0.000 claims 1
• 229920003211 cis-1,4-polyisoprene Polymers 0.000 claims 1
• 238000004132 cross linking Methods 0.000 claims 1
• 239000003431 cross linking reagent Substances 0.000 claims 1
• 150000001924 cycloalkanes Chemical class 0.000 claims 1
• 238000010528 free radical solution polymerization reaction Methods 0.000 claims 1
• 229910052736 halogen Inorganic materials 0.000 claims 1
• 230000002140 halogenating effect Effects 0.000 claims 1
• 150000002367 halogens Chemical group 0.000 claims 1
• 229920003049 isoprene rubber Polymers 0.000 claims 1
• 238000004519 manufacturing process Methods 0.000 claims 1
• 229920001195 polyisoprene Polymers 0.000 claims 1
• 229920001296 polysiloxane Polymers 0.000 claims 1
• 229920006395 saturated elastomer Chemical group 0.000 claims 1
• 239000000377 silicon dioxide Substances 0.000 claims 1
• 229920003048 styrene butadiene rubber Polymers 0.000 claims 1
• 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 1
• 238000010059 sulfur vulcanization Methods 0.000 claims 1
• 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
• 229920002554 vinyl polymer Polymers 0.000 claims 1
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3