JP2001114970A5 - - Google Patents

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Publication number: JP2001114970A5
Authority: JP; Japan
Prior art keywords: group; polymer; compound; diolefin; rubber
Prior art date: 1999-10-19
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

Application number

JP1999297494A

Other languages

English (en)

Japanese (ja)

Other versions

JP2001114970A (ja

JP4491868B2 (ja

Filing date

1999-10-19

Publication date

2006-04-20

1999-10-19 Application filed filed Critical

1999-10-19 Priority to JP29749499A priority Critical patent/JP4491868B2/ja

1999-10-19 Priority claimed from JP29749499A external-priority patent/JP4491868B2/ja

2001-04-24 Publication of JP2001114970A publication Critical patent/JP2001114970A/ja

2006-04-20 Publication of JP2001114970A5 publication Critical patent/JP2001114970A5/ja

2010-06-30 Application granted granted Critical

2010-06-30 Publication of JP4491868B2 publication Critical patent/JP4491868B2/ja

2019-10-19 Anticipated expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

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229920000642 polymer Polymers 0.000 description 90
-1 aromatic vinyl compound Chemical class 0.000 description 79
239000000203 mixture Substances 0.000 description 79
150000001993 dienes Chemical class 0.000 description 76
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 74
229920001577 copolymer Polymers 0.000 description 57
229920001971 elastomer Polymers 0.000 description 53
239000005060 rubber Substances 0.000 description 53
239000000377 silicon dioxide Substances 0.000 description 45
238000006116 polymerization reaction Methods 0.000 description 33
239000000945 filler Substances 0.000 description 27
150000001875 compounds Chemical class 0.000 description 24
239000003921 oil Substances 0.000 description 22
OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 19
239000006229 carbon black Substances 0.000 description 19
125000003277 amino group Chemical group 0.000 description 17
239000004606 Fillers/Extenders Substances 0.000 description 12
238000006243 chemical reaction Methods 0.000 description 11
229910052783 alkali metal Inorganic materials 0.000 description 10
125000004432 carbon atoms Chemical group C* 0.000 description 10
238000004073 vulcanization Methods 0.000 description 10
238000005299 abrasion Methods 0.000 description 9
125000005370 alkoxysilyl group Chemical group 0.000 description 9
125000002887 hydroxy group Chemical group [H]O* 0.000 description 9
239000003999 initiator Substances 0.000 description 9
238000004519 manufacturing process Methods 0.000 description 9
229910052757 nitrogen Inorganic materials 0.000 description 9
229910052718 tin Inorganic materials 0.000 description 9
ATJFFYVFTNAWJD-UHFFFAOYSA-N tin hydride Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 9
125000000217 alkyl group Chemical group 0.000 description 8
OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 8
PPBRXRYQALVLMV-UHFFFAOYSA-N styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 8
125000003118 aryl group Chemical group 0.000 description 7
150000002430 hydrocarbons Chemical class 0.000 description 7
239000002904 solvent Substances 0.000 description 7
VTYYLEPIZMXCLO-UHFFFAOYSA-L calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
MZRVEZGGRBJDDB-UHFFFAOYSA-N n-butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
125000004183 alkoxy alkyl group Chemical group 0.000 description 5
125000003710 aryl alkyl group Chemical group 0.000 description 5
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 5
125000000753 cycloalkyl group Chemical group 0.000 description 5
125000000524 functional group Chemical group 0.000 description 5
229910052751 metal Inorganic materials 0.000 description 5
239000002184 metal Substances 0.000 description 5
238000002156 mixing Methods 0.000 description 5
239000004215 Carbon black (E152) Substances 0.000 description 4
239000006087 Silane Coupling Agent Substances 0.000 description 4
BSYVTEYKTMYBMK-UHFFFAOYSA-N Tetrahydro-2-furanmethanol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 description 4
239000001089 [(2R)-oxolan-2-yl]methanol Substances 0.000 description 4
235000020127 ayran Nutrition 0.000 description 4
KAKZBPTYRLMSJV-UHFFFAOYSA-N butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
230000000694 effects Effects 0.000 description 4
RRHGJUQNOFWUDK-UHFFFAOYSA-N isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
239000002480 mineral oil Substances 0.000 description 4
235000010446 mineral oil Nutrition 0.000 description 4
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
238000005096 rolling process Methods 0.000 description 4
WYURNTSHIVDZCO-UHFFFAOYSA-N tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
150000003606 tin compounds Chemical class 0.000 description 4
DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 3
229960003563 Calcium Carbonate Drugs 0.000 description 3
ZLNQQNXFFQJAID-UHFFFAOYSA-L Magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 3
238000010521 absorption reaction Methods 0.000 description 3
150000001339 alkali metal compounds Chemical class 0.000 description 3
WVDDGKGOMKODPV-UHFFFAOYSA-N benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
229910000019 calcium carbonate Inorganic materials 0.000 description 3
239000011203 carbon fibre reinforced carbon Substances 0.000 description 3
150000001728 carbonyl compounds Chemical class 0.000 description 3
239000004927 clay Substances 0.000 description 3
229910052570 clay Inorganic materials 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
238000001035 drying Methods 0.000 description 3
125000004435 hydrogen atoms Chemical group [H]* 0.000 description 3
239000001095 magnesium carbonate Substances 0.000 description 3
239000011776 magnesium carbonate Substances 0.000 description 3
229910000021 magnesium carbonate Inorganic materials 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
239000002245 particle Substances 0.000 description 3
230000000704 physical effect Effects 0.000 description 3
NQRYJNQNLNOLGT-UHFFFAOYSA-N piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 3
230000003014 reinforcing Effects 0.000 description 3
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 3
229910000077 silane Inorganic materials 0.000 description 3
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-Tetramethylpiperidine Chemical compound CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 2
UJOBWOGCFQCDNV-UHFFFAOYSA-N Carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 2
HNDIBXFOXXJZIF-UHFFFAOYSA-N ClC[SiH](OC1=CC=CC=C1)OC1=CC=CC=C1 Chemical compound ClC[SiH](OC1=CC=CC=C1)OC1=CC=CC=C1 HNDIBXFOXXJZIF-UHFFFAOYSA-N 0.000 description 2
BFSVOASYOCHEOV-UHFFFAOYSA-N Diethylethanolamine Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 2
240000008528 Hevea brasiliensis Species 0.000 description 2
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 2
BKIMMITUMNQMOS-UHFFFAOYSA-N Nonane Chemical compound CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 2
239000005062 Polybutadiene Substances 0.000 description 2
RSJKGSCJYJTIGS-UHFFFAOYSA-N Undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 description 2
125000002723 alicyclic group Chemical group 0.000 description 2
150000001340 alkali metals Chemical group 0.000 description 2
238000004164 analytical calibration Methods 0.000 description 2
150000001450 anions Chemical class 0.000 description 2
239000010692 aromatic oil Substances 0.000 description 2
238000011088 calibration curve Methods 0.000 description 2
CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
230000000875 corresponding Effects 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
WGPIFVWDQMTOJZ-UHFFFAOYSA-N ethenyl-tris(2-ethylhexoxy)silane Chemical compound CCCCC(CC)CO[Si](OCC(CC)CCCC)(OCC(CC)CCCC)C=C WGPIFVWDQMTOJZ-UHFFFAOYSA-N 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
239000000446 fuel Substances 0.000 description 2
125000001841 imino group Chemical group [H]N=* 0.000 description 2
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
150000002642 lithium compounds Chemical class 0.000 description 2
WGOPGODQLGJZGL-UHFFFAOYSA-N lithium;butane Chemical compound [Li+].CC[CH-]C WGOPGODQLGJZGL-UHFFFAOYSA-N 0.000 description 2
238000010550 living polymerization reaction Methods 0.000 description 2
239000000463 material Substances 0.000 description 2
238000005259 measurement Methods 0.000 description 2
DRXHEPWCWBIQFJ-UHFFFAOYSA-N methyl(triphenoxy)silane Chemical compound C=1C=CC=CC=1O[Si](OC=1C=CC=CC=1)(C)OC1=CC=CC=C1 DRXHEPWCWBIQFJ-UHFFFAOYSA-N 0.000 description 2
238000006011 modification reaction Methods 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N n-butanol Chemical compound CCCCO LRHPLDYGYMQRHN-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
229920001194 natural rubber Polymers 0.000 description 2
DFPAKSUCGFBDDF-UHFFFAOYSA-N nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 description 2
150000002900 organolithium compounds Chemical class 0.000 description 2
229920002857 polybutadiene Polymers 0.000 description 2
229920001195 polyisoprene Polymers 0.000 description 2
239000003505 polymerization initiator Substances 0.000 description 2
RWRDLPDLKQPQOW-UHFFFAOYSA-N pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 2
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
229920003048 styrene butadiene rubber Polymers 0.000 description 2
239000000126 substance Substances 0.000 description 2
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
ZMANZCXQSJIPKH-UHFFFAOYSA-N triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 2
ABDKAPXRBAPSQN-UHFFFAOYSA-N 1,2-Dimethoxybenzene Chemical compound COC1=CC=CC=C1OC ABDKAPXRBAPSQN-UHFFFAOYSA-N 0.000 description 1
LZDKZFUFMNSQCJ-UHFFFAOYSA-N 1,2-diethoxyethane Chemical compound CCOCCOCC LZDKZFUFMNSQCJ-UHFFFAOYSA-N 0.000 description 1
VPBZZPOGZPKYKX-UHFFFAOYSA-N 1,2-diethoxypropane Chemical compound CCOCC(C)OCC VPBZZPOGZPKYKX-UHFFFAOYSA-N 0.000 description 1
LEEANUDEDHYDTG-UHFFFAOYSA-N 1,2-dimethoxypropane Chemical compound COCC(C)OC LEEANUDEDHYDTG-UHFFFAOYSA-N 0.000 description 1
AHWDQDMGFXRVFB-UHFFFAOYSA-N 1,3,5-trimethyl-1,3,5-triazinane-2,4,6-trione Chemical compound CN1C(=O)N(C)C(=O)N(C)C1=O AHWDQDMGFXRVFB-UHFFFAOYSA-N 0.000 description 1
GDXHBFHOEYVPED-UHFFFAOYSA-N 1-(2-butoxyethoxy)butane Chemical compound CCCCOCCOCCCC GDXHBFHOEYVPED-UHFFFAOYSA-N 0.000 description 1
QMGJMGFZLXYHCR-UHFFFAOYSA-N 1-(2-butoxypropoxy)butane Chemical compound CCCCOCC(C)OCCCC QMGJMGFZLXYHCR-UHFFFAOYSA-N 0.000 description 1
UYMQPNRUQXPLCY-UHFFFAOYSA-N 1-(2-piperidin-1-ylethyl)piperidine Chemical compound C1CCCCN1CCN1CCCCC1 UYMQPNRUQXPLCY-UHFFFAOYSA-N 0.000 description 1
OUSXYCTXXLYBGJ-UHFFFAOYSA-N 1-ethenyl-2,4-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=C(C=C)C(C(C)C)=C1 OUSXYCTXXLYBGJ-UHFFFAOYSA-N 0.000 description 1
OEVVKKAVYQFQNV-UHFFFAOYSA-N 1-ethenyl-2,4-dimethylbenzene Chemical compound CC1=CC=C(C=C)C(C)=C1 OEVVKKAVYQFQNV-UHFFFAOYSA-N 0.000 description 1
NVZWEEGUWXZOKI-UHFFFAOYSA-N 1-ethenyl-2-methylbenzene Chemical compound CC1=CC=CC=C1C=C NVZWEEGUWXZOKI-UHFFFAOYSA-N 0.000 description 1
JZHGRUMIRATHIU-UHFFFAOYSA-N 1-ethenyl-3-methylbenzene Chemical compound CC1=CC=CC(C=C)=C1 JZHGRUMIRATHIU-UHFFFAOYSA-N 0.000 description 1
JLBJTVDPSNHSKJ-UHFFFAOYSA-N 1-ethenyl-4-methylbenzene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
WGCYRFWNGRMRJA-UHFFFAOYSA-N 1-ethylpiperazine Chemical compound CCN1CCNCC1 WGCYRFWNGRMRJA-UHFFFAOYSA-N 0.000 description 1
QEDJMOONZLUIMC-UHFFFAOYSA-N 1-tert-butyl-4-ethenylbenzene Chemical compound CC(C)(C)C1=CC=C(C=C)C=C1 QEDJMOONZLUIMC-UHFFFAOYSA-N 0.000 description 1
SDJHPPZKZZWAKF-UHFFFAOYSA-N 2,3-dimethylbuta-1,3-diene Chemical compound CC(=C)C(C)=C SDJHPPZKZZWAKF-UHFFFAOYSA-N 0.000 description 1
ZEBFPAXSQXIPNF-UHFFFAOYSA-N 2,5-dimethylpyrrolidine Chemical compound CC1CCC(C)N1 ZEBFPAXSQXIPNF-UHFFFAOYSA-N 0.000 description 1
HNVIQLPOGUDBSU-UHFFFAOYSA-N 2,6-dimethylmorpholine Chemical compound CC1CNCC(C)O1 HNVIQLPOGUDBSU-UHFFFAOYSA-N 0.000 description 1
IFNWESYYDINUHV-UHFFFAOYSA-N 2,6-dimethylpiperazine Chemical compound CC1CNCC(C)N1 IFNWESYYDINUHV-UHFFFAOYSA-N 0.000 description 1
KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-Vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
FXRQXYSJYZPGJZ-UHFFFAOYSA-N 2-[(2-methylpropan-2-yl)oxy]ethenylbenzene Chemical compound CC(C)(C)OC=CC1=CC=CC=C1 FXRQXYSJYZPGJZ-UHFFFAOYSA-N 0.000 description 1
TYENDWOHUUAIJH-UHFFFAOYSA-N 2-[(4-ethenylphenyl)methoxy]-N,N-dimethylethanamine Chemical compound CN(C)CCOCC1=CC=C(C=C)C=C1 TYENDWOHUUAIJH-UHFFFAOYSA-N 0.000 description 1
SAIKULLUBZKPDA-UHFFFAOYSA-N 2-ethyl-N-(2-ethylhexyl)hexan-1-amine Chemical compound CCCCC(CC)CNCC(CC)CCCC SAIKULLUBZKPDA-UHFFFAOYSA-N 0.000 description 1
JOMNTHCQHJPVAZ-UHFFFAOYSA-N 2-methylpiperazine Chemical compound CC1CNCCN1 JOMNTHCQHJPVAZ-UHFFFAOYSA-N 0.000 description 1
CDODDZJCEADUQQ-UHFFFAOYSA-N 3,3-dimethylpiperidine Chemical compound CC1(C)CCCNC1 CDODDZJCEADUQQ-UHFFFAOYSA-N 0.000 description 1
KQVVPOMBWBKNRS-UHFFFAOYSA-N 3-(1,3-benzothiazol-2-yl)propyl-triethoxysilane Chemical compound C1=CC=C2SC(CCC[Si](OCC)(OCC)OCC)=NC2=C1 KQVVPOMBWBKNRS-UHFFFAOYSA-N 0.000 description 1
UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 1
JCQLPDZCNSVBMS-UHFFFAOYSA-N 5-phenylmethoxy-1H-indole Chemical compound C=1C=C2NC=CC2=CC=1OCC1=CC=CC=C1 JCQLPDZCNSVBMS-UHFFFAOYSA-N 0.000 description 1
XXROGKLTLUQVRX-UHFFFAOYSA-N Allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 1
ZSIQJIWKELUFRJ-UHFFFAOYSA-N Azepane Chemical compound C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 description 1
HONIICLYMWZJFZ-UHFFFAOYSA-N Azetidine Chemical compound C1CNC1 HONIICLYMWZJFZ-UHFFFAOYSA-N 0.000 description 1
QXNDZONIWRINJR-UHFFFAOYSA-N Azocane Chemical compound C1CCCNCCC1 QXNDZONIWRINJR-UHFFFAOYSA-N 0.000 description 1
IQXXEPZFOOTTBA-UHFFFAOYSA-N Benzylpiperazine Chemical compound C=1C=CC=CC=1CN1CCNCC1 IQXXEPZFOOTTBA-UHFFFAOYSA-N 0.000 description 1
VMNAIGYESZZLBW-UHFFFAOYSA-N BrC=C[SiH](OC1=CC=CC=C1)OC1=CC=CC=C1 Chemical compound BrC=C[SiH](OC1=CC=CC=C1)OC1=CC=CC=C1 VMNAIGYESZZLBW-UHFFFAOYSA-N 0.000 description 1
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
HKLWRZOMRLDVOF-UHFFFAOYSA-N C(C)C=C[SiH](OC1=CC=CC=C1)OC1=CC=CC=C1 Chemical compound C(C)C=C[SiH](OC1=CC=CC=C1)OC1=CC=CC=C1 HKLWRZOMRLDVOF-UHFFFAOYSA-N 0.000 description 1
FDBTWYMUCCHKHD-UHFFFAOYSA-N CC=C[SiH](OCC(CCCC)CC)OCC(CCCC)CC Chemical compound CC=C[SiH](OCC(CCCC)CC)OCC(CCCC)CC FDBTWYMUCCHKHD-UHFFFAOYSA-N 0.000 description 1
VAQYLPPYXNKZGG-UHFFFAOYSA-N CCC(C)CO[SiH](CCl)OCC(C)CC Chemical compound CCC(C)CO[SiH](CCl)OCC(C)CC VAQYLPPYXNKZGG-UHFFFAOYSA-N 0.000 description 1
FTJVOUKRKPQVRL-UHFFFAOYSA-N CCCCC(CC)CO[SiH3] Chemical compound CCCCC(CC)CO[SiH3] FTJVOUKRKPQVRL-UHFFFAOYSA-N 0.000 description 1
RZTBGMHNZCSDFA-UHFFFAOYSA-N CCCCC(CC)CO[SiH](CCl)OCC(CC)CCCC Chemical compound CCCCC(CC)CO[SiH](CCl)OCC(CC)CCCC RZTBGMHNZCSDFA-UHFFFAOYSA-N 0.000 description 1
ZXIPAKVMYCMVEQ-UHFFFAOYSA-N CCO[Si](OCC)(OCC)CCCS=C(N(C)C)SSSSC(N(C)C)=SCCC[Si](OCC)(OCC)OCC Chemical compound CCO[Si](OCC)(OCC)CCCS=C(N(C)C)SSSSC(N(C)C)=SCCC[Si](OCC)(OCC)OCC ZXIPAKVMYCMVEQ-UHFFFAOYSA-N 0.000 description 1
YACLQRRMGMJLJV-UHFFFAOYSA-N Chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
KZJADWHHDAAILD-UHFFFAOYSA-N ClC=C[SiH](OCC(CCCC)CC)OCC(CCCC)CC Chemical compound ClC=C[SiH](OCC(CCCC)CC)OCC(CCCC)CC KZJADWHHDAAILD-UHFFFAOYSA-N 0.000 description 1
ZFSLODLOARCGLH-UHFFFAOYSA-N Cyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
150000007973 Cyanuric acids Chemical class 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N Cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
JQVDAXLFBXTEQA-UHFFFAOYSA-N Dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 1
XBPCUCUWBYBCDP-UHFFFAOYSA-N Dicyclohexylamine Chemical compound C1CCCCC1NC1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-N 0.000 description 1
HPNMFZURTQLUMO-UHFFFAOYSA-N Diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
SBZXBUIDTXKZTM-UHFFFAOYSA-N Diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
WEHWNAOGRSTTBQ-UHFFFAOYSA-N Dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 1
HEZNVIYQEUHLNI-UHFFFAOYSA-N Ethiofencarb Chemical compound CCSCC1=CC=CC=C1OC(=O)NC HEZNVIYQEUHLNI-UHFFFAOYSA-N 0.000 description 1
229920002456 HOTAIR Polymers 0.000 description 1
238000004566 IR spectroscopy Methods 0.000 description 1
239000006237 Intermediate SAF Substances 0.000 description 1
AFRJJFRNGGLMDW-UHFFFAOYSA-N Lithium amide Chemical compound [Li+].[NH2-] AFRJJFRNGGLMDW-UHFFFAOYSA-N 0.000 description 1
JFTBTTPUYRGXDG-UHFFFAOYSA-N Methyl violet Chemical compound Cl.C1=CC(=NC)C=CC1=C(C=1C=CC(=CC=1)N(C)C)C1=CC=C(N(C)C)C=C1 JFTBTTPUYRGXDG-UHFFFAOYSA-N 0.000 description 1
UBHHTPOLMACCDD-UHFFFAOYSA-N N,N-dimethyl-4-phenylbut-3-en-1-amine Chemical compound CN(C)CCC=CC1=CC=CC=C1 UBHHTPOLMACCDD-UHFFFAOYSA-N 0.000 description 1
XTAZYLNFDRKIHJ-UHFFFAOYSA-N N,N-dioctyloctan-1-amine Chemical compound CCCCCCCCN(CCCCCCCC)CCCCCCCC XTAZYLNFDRKIHJ-UHFFFAOYSA-N 0.000 description 1
DZRKBPWATCKLKY-UHFFFAOYSA-N N-benzyl-N-methylprop-2-en-1-amine Chemical compound C=CCN(C)CC1=CC=CC=C1 DZRKBPWATCKLKY-UHFFFAOYSA-N 0.000 description 1
OBYVIBDTOCAXSN-UHFFFAOYSA-N N-butan-2-ylbutan-2-amine Chemical compound CCC(C)NC(C)CC OBYVIBDTOCAXSN-UHFFFAOYSA-N 0.000 description 1
UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
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ADLSSRLDGACTEX-UHFFFAOYSA-N tetraphenyl silicate Chemical compound C=1C=CC=CC=1O[Si](OC=1C=CC=CC=1)(OC=1C=CC=CC=1)OC1=CC=CC=C1 ADLSSRLDGACTEX-UHFFFAOYSA-N 0.000 description 1
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ASAOXGWSIOQTDI-UHFFFAOYSA-N triethoxy-[2-(2-triethoxysilylethyltetrasulfanyl)ethyl]silane Chemical compound CCO[Si](OCC)(OCC)CCSSSSCC[Si](OCC)(OCC)OCC ASAOXGWSIOQTDI-UHFFFAOYSA-N 0.000 description 1
VTHOKNTVYKTUPI-UHFFFAOYSA-N triethoxy-[3-(3-triethoxysilylpropyltetrasulfanyl)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCSSSSCCC[Si](OCC)(OCC)OCC VTHOKNTVYKTUPI-UHFFFAOYSA-N 0.000 description 1
DVYQCRRVXOXJSA-UHFFFAOYSA-N tris(2-ethylhexoxy)-methylsilane Chemical compound CCCCC(CC)CO[Si](C)(OCC(CC)CCCC)OCC(CC)CCCC DVYQCRRVXOXJSA-UHFFFAOYSA-N 0.000 description 1
125000002948 undecyl 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])[H] 0.000 description 1
239000004636 vulcanized rubber Substances 0.000 description 1
238000005406 washing Methods 0.000 description 1
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125000005023 xylyl group Chemical group 0.000 description 1
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JP29749499A 1999-10-19 1999-10-19 ジオレフィン系重合体組成物の製造方法、および加硫用ゴム組成物の製造方法 Expired - Fee Related JP4491868B2 (ja)

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JP3625919B2 (ja) *	1995-10-16	2005-03-02	株式会社ブリヂストン	重合体の製造方法
JPH10218920A (ja) *	1997-02-05	1998-08-18	Bridgestone Corp	共役ジエン系重合体及びそのゴム組成物
JPH11246633A (ja) *	1997-12-16	1999-09-14	Jsr Corp	共役ジオレフィン系共重合体ゴムおよびその組成物
JP4348795B2 (ja) *	1999-10-19	2009-10-21	Ｊｓｒ株式会社	ジオレフィン系重合体組成物、その製造方法、および加硫用ゴム組成物

1999
- 1999-10-19 JP JP29749499A patent/JP4491868B2/ja not_active Expired - Fee Related

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