ES2222004T3 - Caucho de estireno-butadieno, de emulsion. - Google Patents
Caucho de estireno-butadieno, de emulsion.Info
- Publication number
- ES2222004T3 ES2222004T3 ES99104756T ES99104756T ES2222004T3 ES 2222004 T3 ES2222004 T3 ES 2222004T3 ES 99104756 T ES99104756 T ES 99104756T ES 99104756 T ES99104756 T ES 99104756T ES 2222004 T3 ES2222004 T3 ES 2222004T3
- Authority
- ES
- Spain
- Prior art keywords
- styrene
- rubber
- butadiene
- molecular weight
- butadiene rubber
- 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 - Lifetime
Links
- 239000000839 emulsion Substances 0.000 title claims abstract description 107
- 229920003048 styrene butadiene rubber Polymers 0.000 title claims description 363
- 229920001971 elastomer Polymers 0.000 claims abstract description 241
- 239000005060 rubber Substances 0.000 claims abstract description 241
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 207
- 239000000203 mixture Substances 0.000 claims abstract description 202
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims abstract description 97
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical group C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims abstract description 81
- 238000003860 storage Methods 0.000 claims abstract description 16
- 230000003252 repetitive effect Effects 0.000 claims abstract description 11
- 239000002174 Styrene-butadiene Substances 0.000 claims description 265
- 239000011115 styrene butadiene Substances 0.000 claims description 76
- 238000006116 polymerization reaction Methods 0.000 claims description 75
- 238000000034 method Methods 0.000 claims description 66
- 239000000178 monomer Substances 0.000 claims description 64
- 229920000126 latex Polymers 0.000 claims description 54
- 239000004816 latex Substances 0.000 claims description 42
- 239000000344 soap Substances 0.000 claims description 40
- 229920001195 polyisoprene Polymers 0.000 claims description 38
- 238000006243 chemical reaction Methods 0.000 claims description 34
- 229920003193 cis-1,4-polybutadiene polymer Polymers 0.000 claims description 20
- 229920002857 polybutadiene Polymers 0.000 claims description 20
- 150000003254 radicals Chemical class 0.000 claims description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 19
- 239000005062 Polybutadiene Substances 0.000 claims description 17
- 229920001194 natural rubber Polymers 0.000 claims description 16
- 244000043261 Hevea brasiliensis Species 0.000 claims description 15
- 238000002156 mixing Methods 0.000 claims description 15
- 229920003052 natural elastomer Polymers 0.000 claims description 15
- 238000007334 copolymerization reaction Methods 0.000 claims description 11
- 238000005194 fractionation Methods 0.000 claims description 9
- 239000003995 emulsifying agent Substances 0.000 claims description 7
- 229920002554 vinyl polymer Polymers 0.000 claims description 7
- 230000008569 process Effects 0.000 claims description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 6
- 238000001495 thermal field-flow fractionation Methods 0.000 claims description 5
- 230000010355 oscillation Effects 0.000 claims description 4
- VLLYOYVKQDKAHN-UHFFFAOYSA-N buta-1,3-diene;2-methylbuta-1,3-diene Chemical compound C=CC=C.CC(=C)C=C VLLYOYVKQDKAHN-UHFFFAOYSA-N 0.000 claims description 3
- 238000005345 coagulation Methods 0.000 claims description 3
- 230000015271 coagulation Effects 0.000 claims description 3
- 229920003194 trans-1,4-polybutadiene polymer Polymers 0.000 claims description 3
- ROGIWVXWXZRRMZ-UHFFFAOYSA-N 2-methylbuta-1,3-diene;styrene Chemical compound CC(=C)C=C.C=CC1=CC=CC=C1 ROGIWVXWXZRRMZ-UHFFFAOYSA-N 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 229920005683 SIBR Polymers 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 36
- 229910052717 sulfur Inorganic materials 0.000 abstract description 25
- 238000004519 manufacturing process Methods 0.000 abstract description 15
- 239000006185 dispersion Substances 0.000 abstract description 6
- 238000010586 diagram Methods 0.000 abstract 2
- 239000012530 fluid Substances 0.000 abstract 1
- 238000010408 sweeping Methods 0.000 abstract 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 60
- 239000000377 silicon dioxide Substances 0.000 description 29
- -1 dodecylmercaptane Chemical compound 0.000 description 28
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 24
- 239000011593 sulfur Substances 0.000 description 24
- 239000000243 solution Substances 0.000 description 23
- 229920000642 polymer Polymers 0.000 description 22
- 239000006229 carbon black Substances 0.000 description 21
- 239000003795 chemical substances by application Substances 0.000 description 17
- 239000003921 oil Substances 0.000 description 15
- 239000003963 antioxidant agent Substances 0.000 description 13
- 239000003999 initiator Substances 0.000 description 13
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 12
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 11
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 11
- 230000003078 antioxidant effect Effects 0.000 description 11
- 230000002829 reductive effect Effects 0.000 description 11
- 238000005096 rolling process Methods 0.000 description 11
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 11
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 10
- 238000007720 emulsion polymerization reaction Methods 0.000 description 10
- 239000011347 resin Substances 0.000 description 10
- 229920005989 resin Polymers 0.000 description 10
- 230000015572 biosynthetic process Effects 0.000 description 9
- 239000012086 standard solution Substances 0.000 description 9
- 206010033307 Overweight Diseases 0.000 description 8
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 8
- 239000002253 acid Substances 0.000 description 8
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 235000014113 dietary fatty acids Nutrition 0.000 description 8
- 239000000194 fatty acid Substances 0.000 description 8
- 229930195729 fatty acid Natural products 0.000 description 8
- 150000004665 fatty acids Chemical class 0.000 description 8
- DEQZTKGFXNUBJL-UHFFFAOYSA-N n-(1,3-benzothiazol-2-ylsulfanyl)cyclohexanamine Chemical compound C1CCCCC1NSC1=NC2=CC=CC=C2S1 DEQZTKGFXNUBJL-UHFFFAOYSA-N 0.000 description 8
- 230000000704 physical effect Effects 0.000 description 8
- 239000011591 potassium Substances 0.000 description 8
- 238000012545 processing Methods 0.000 description 8
- 125000003118 aryl group Chemical group 0.000 description 7
- 238000002474 experimental method Methods 0.000 description 7
- 229910052700 potassium Inorganic materials 0.000 description 7
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 7
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 6
- 238000009472 formulation Methods 0.000 description 6
- 239000012188 paraffin wax Substances 0.000 description 6
- 238000010058 rubber compounding Methods 0.000 description 6
- 239000011787 zinc oxide Substances 0.000 description 6
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 5
- 238000005516 engineering process Methods 0.000 description 5
- 239000004200 microcrystalline wax Substances 0.000 description 5
- 235000019808 microcrystalline wax Nutrition 0.000 description 5
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 230000000930 thermomechanical effect Effects 0.000 description 5
- 241000234671 Ananas Species 0.000 description 4
- 235000007119 Ananas comosus Nutrition 0.000 description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
- 239000012190 activator Substances 0.000 description 4
- 238000000149 argon plasma sintering Methods 0.000 description 4
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 4
- 238000011068 loading method Methods 0.000 description 4
- 239000003607 modifier Substances 0.000 description 4
- 159000000000 sodium salts Chemical class 0.000 description 4
- 239000003760 tallow Substances 0.000 description 4
- RYCLIXPGLDDLTM-UHFFFAOYSA-J tetrapotassium;phosphonato phosphate Chemical compound [K+].[K+].[K+].[K+].[O-]P([O-])(=O)OP([O-])([O-])=O RYCLIXPGLDDLTM-UHFFFAOYSA-J 0.000 description 4
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 4
- 229960002447 thiram Drugs 0.000 description 4
- 229910052725 zinc Inorganic materials 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- 241001441571 Hiodontidae Species 0.000 description 3
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 230000000670 limiting effect Effects 0.000 description 3
- 150000003961 organosilicon compounds Chemical class 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 3
- 239000003352 sequestering agent Substances 0.000 description 3
- 239000008149 soap solution Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 230000003068 static effect Effects 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- ZNRLMGFXSPUZNR-UHFFFAOYSA-N 2,2,4-trimethyl-1h-quinoline Chemical compound C1=CC=C2C(C)=CC(C)(C)NC2=C1 ZNRLMGFXSPUZNR-UHFFFAOYSA-N 0.000 description 2
- YAJYJWXEWKRTPO-UHFFFAOYSA-N 2,3,3,4,4,5-hexamethylhexane-2-thiol Chemical compound CC(C)C(C)(C)C(C)(C)C(C)(C)S YAJYJWXEWKRTPO-UHFFFAOYSA-N 0.000 description 2
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- RSWGJHLUYNHPMX-ONCXSQPRSA-N abietic acid Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(O)=O RSWGJHLUYNHPMX-ONCXSQPRSA-N 0.000 description 2
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium peroxydisulfate Substances [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- VAZSKTXWXKYQJF-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)OOS([O-])=O VAZSKTXWXKYQJF-UHFFFAOYSA-N 0.000 description 2
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 239000012267 brine Substances 0.000 description 2
- 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 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 230000001112 coagulating effect Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 229960002380 dibutyl phthalate Drugs 0.000 description 2
- IJKVHSBPTUYDLN-UHFFFAOYSA-N dihydroxy(oxo)silane Chemical compound O[Si](O)=O IJKVHSBPTUYDLN-UHFFFAOYSA-N 0.000 description 2
- 229940071106 ethylenediaminetetraacetate Drugs 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 150000002978 peroxides Chemical group 0.000 description 2
- 239000011414 polymer cement Substances 0.000 description 2
- 239000001103 potassium chloride Substances 0.000 description 2
- 235000011164 potassium chloride Nutrition 0.000 description 2
- 235000019394 potassium persulphate Nutrition 0.000 description 2
- 238000010526 radical polymerization reaction Methods 0.000 description 2
- 230000003014 reinforcing effect Effects 0.000 description 2
- 239000000779 smoke Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- VYGBQXDNOUHIBZ-UHFFFAOYSA-L sodium formaldehyde sulphoxylate Chemical compound [Na+].[Na+].O=C.[O-]S[O-] VYGBQXDNOUHIBZ-UHFFFAOYSA-L 0.000 description 2
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 125000006850 spacer group Chemical group 0.000 description 2
- 238000010561 standard procedure Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000002194 synthesizing effect Effects 0.000 description 2
- 229920003051 synthetic elastomer Polymers 0.000 description 2
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- CORMBJOFDGICKF-UHFFFAOYSA-N 1,3,5-trimethoxy 2-vinyl benzene Natural products COC1=CC(OC)=C(C=C)C(OC)=C1 CORMBJOFDGICKF-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
- LGJCFVYMIJLQJO-UHFFFAOYSA-N 1-dodecylperoxydodecane Chemical compound CCCCCCCCCCCCOOCCCCCCCCCCCC LGJCFVYMIJLQJO-UHFFFAOYSA-N 0.000 description 1
- YHOMZMOAUNOPCN-UHFFFAOYSA-N 1-ethenyl-2,3,4,5-tetraethylbenzene Chemical compound CCC1=CC(C=C)=C(CC)C(CC)=C1CC YHOMZMOAUNOPCN-UHFFFAOYSA-N 0.000 description 1
- HVOKBODBWQEEGI-UHFFFAOYSA-N 1-ethenyl-3,5-diethylbenzene Chemical compound CCC1=CC(CC)=CC(C=C)=C1 HVOKBODBWQEEGI-UHFFFAOYSA-N 0.000 description 1
- XSHXURIGVYRXAD-UHFFFAOYSA-N 1-ethenyl-3,5-diphenylbenzene Chemical compound C=1C(C=C)=CC(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 XSHXURIGVYRXAD-UHFFFAOYSA-N 0.000 description 1
- LFZRKMOWVSTEMD-UHFFFAOYSA-N 1-ethenyl-3-ethylnaphthalene Chemical compound C1=CC=CC2=CC(CC)=CC(C=C)=C21 LFZRKMOWVSTEMD-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
- VVTGQMLRTKFKAM-UHFFFAOYSA-N 1-ethenyl-4-propylbenzene Chemical compound CCCC1=CC=C(C=C)C=C1 VVTGQMLRTKFKAM-UHFFFAOYSA-N 0.000 description 1
- ZUJBNWMWGTYWMW-UHFFFAOYSA-N 1-ethenyl-6-propan-2-ylnaphthalene Chemical compound C=CC1=CC=CC2=CC(C(C)C)=CC=C21 ZUJBNWMWGTYWMW-UHFFFAOYSA-N 0.000 description 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 1
- 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
- ABERXULXRGIGTD-UHFFFAOYSA-N 2-dodecyl-7-ethenylnaphthalene Chemical compound C1=CC(C=C)=CC2=CC(CCCCCCCCCCCC)=CC=C21 ABERXULXRGIGTD-UHFFFAOYSA-N 0.000 description 1
- PDELBHCVXBSVPJ-UHFFFAOYSA-N 2-ethenyl-1,3,5-trimethylbenzene Chemical compound CC1=CC(C)=C(C=C)C(C)=C1 PDELBHCVXBSVPJ-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- DXFURPHVJQITAC-UHFFFAOYSA-N 4-benzyl-1-ethenyl-2-ethylbenzene Chemical compound C1=C(C=C)C(CC)=CC(CC=2C=CC=CC=2)=C1 DXFURPHVJQITAC-UHFFFAOYSA-N 0.000 description 1
- QJRVOJKLQNSNDB-UHFFFAOYSA-N 4-dodecan-3-ylbenzenesulfonic acid Chemical compound CCCCCCCCCC(CC)C1=CC=C(S(O)(=O)=O)C=C1 QJRVOJKLQNSNDB-UHFFFAOYSA-N 0.000 description 1
- GYLGGODPGFTNRX-UHFFFAOYSA-N 6-cyclohexyl-1-ethenylnaphthalene Chemical compound C=1C=C2C(C=C)=CC=CC2=CC=1C1CCCCC1 GYLGGODPGFTNRX-UHFFFAOYSA-N 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000238586 Cirripedia Species 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 229920001174 Diethylhydroxylamine Polymers 0.000 description 1
- 239000004908 Emulsion polymer Substances 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- RSPISYXLHRIGJD-UHFFFAOYSA-N OOOO Chemical compound OOOO RSPISYXLHRIGJD-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000007630 basic procedure Methods 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 239000003738 black carbon Substances 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000012986 chain transfer agent Substances 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
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- 230000008878 coupling Effects 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
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- 239000006071 cream Substances 0.000 description 1
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- 125000000000 cycloalkoxy group Chemical group 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- BSVQJWUUZCXSOL-UHFFFAOYSA-N cyclohexylsulfonyl ethaneperoxoate Chemical compound CC(=O)OOS(=O)(=O)C1CCCCC1 BSVQJWUUZCXSOL-UHFFFAOYSA-N 0.000 description 1
- 238000013480 data collection Methods 0.000 description 1
- XJOBOFWTZOKMOH-UHFFFAOYSA-N decanoyl decaneperoxoate Chemical compound CCCCCCCCCC(=O)OOC(=O)CCCCCCCCC XJOBOFWTZOKMOH-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- FVCOIAYSJZGECG-UHFFFAOYSA-N diethylhydroxylamine Chemical compound CCN(O)CC FVCOIAYSJZGECG-UHFFFAOYSA-N 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000001825 field-flow fractionation Methods 0.000 description 1
- ISXSFOPKZQZDAO-UHFFFAOYSA-N formaldehyde;sodium Chemical compound [Na].O=C ISXSFOPKZQZDAO-UHFFFAOYSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- QWVBGCWRHHXMRM-UHFFFAOYSA-N hexadecoxycarbonyloxy hexadecyl carbonate Chemical compound CCCCCCCCCCCCCCCCOC(=O)OOC(=O)OCCCCCCCCCCCCCCCC QWVBGCWRHHXMRM-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- ZQMHJBXHRFJKOT-UHFFFAOYSA-N methyl 2-[(1-methoxy-2-methyl-1-oxopropan-2-yl)diazenyl]-2-methylpropanoate Chemical compound COC(=O)C(C)(C)N=NC(C)(C)C(=O)OC ZQMHJBXHRFJKOT-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
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- 239000003960 organic solvent Substances 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
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- HDBWAWNLGGMZRQ-UHFFFAOYSA-N p-Vinylbiphenyl Chemical compound C1=CC(C=C)=CC=C1C1=CC=CC=C1 HDBWAWNLGGMZRQ-UHFFFAOYSA-N 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
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- 239000011148 porous material Substances 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
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- XWGJFPHUCFXLBL-UHFFFAOYSA-M rongalite Chemical compound [Na+].OCS([O-])=O XWGJFPHUCFXLBL-UHFFFAOYSA-M 0.000 description 1
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- 239000011780 sodium chloride Substances 0.000 description 1
- NUTBUHYTTNKZOR-UHFFFAOYSA-M sodium;n,n-dimethylcarbamothioate Chemical compound [Na+].CN(C)C([O-])=S NUTBUHYTTNKZOR-UHFFFAOYSA-M 0.000 description 1
- 239000008234 soft water Substances 0.000 description 1
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- 238000012360 testing method Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000012549 training Methods 0.000 description 1
- XQCNPXMIHJAHGO-UHFFFAOYSA-N trimethoxy-[(trimethoxysilylmethyltetrasulfanyl)methyl]silane Chemical compound CO[Si](OC)(OC)CSSSSC[Si](OC)(OC)OC XQCNPXMIHJAHGO-UHFFFAOYSA-N 0.000 description 1
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
- C08L9/06—Copolymers with styrene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60C—VEHICLE TYRES; TYRE INFLATION; TYRE CHANGING; CONNECTING VALVES TO INFLATABLE ELASTIC BODIES IN GENERAL; DEVICES OR ARRANGEMENTS RELATED TO TYRES
- B60C1/00—Tyres characterised by the chemical composition or the physical arrangement or mixture of the composition
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60C—VEHICLE TYRES; TYRE INFLATION; TYRE CHANGING; CONNECTING VALVES TO INFLATABLE ELASTIC BODIES IN GENERAL; DEVICES OR ARRANGEMENTS RELATED TO TYRES
- B60C1/00—Tyres characterised by the chemical composition or the physical arrangement or mixture of the composition
- B60C1/0016—Compositions of the tread
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F236/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
- C08F236/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
- C08F236/04—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
- C08F236/10—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated with vinyl-aromatic monomers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F6/00—Post-polymerisation treatments
- C08F6/14—Treatment of polymer emulsions
- C08F6/22—Coagulation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/12—Powdering or granulating
- C08J3/16—Powdering or granulating by coagulating dispersions
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
- C08L25/08—Copolymers of styrene
- C08L25/10—Copolymers of styrene with conjugated dienes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2030/00—Pneumatic or solid tyres or parts thereof
- B29L2030/002—Treads
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02T—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
- Y02T10/00—Road transport of goods or passengers
- Y02T10/80—Technologies aiming to reduce greenhouse gasses emissions common to all road transportation technologies
- Y02T10/86—Optimisation of rolling resistance, e.g. weight reduction
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T152/00—Resilient tires and wheels
- Y10T152/10—Tires, resilient
- Y10T152/10495—Pneumatic tire or inner tube
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Dispersion Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Tires In General (AREA)
- Polymerisation Methods In General (AREA)
- Graft Or Block Polymers (AREA)
Applications Claiming Priority (12)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11366398P | 1998-03-11 | 1998-03-11 | |
| US113663P | 1998-03-11 | ||
| US7978998P | 1998-03-28 | 1998-03-28 | |
| US79789P | 1998-03-28 | ||
| US10475598P | 1998-10-19 | 1998-10-19 | |
| US104755P | 1998-10-19 | ||
| US10953098P | 1998-11-23 | 1998-11-23 | |
| US109530P | 1998-11-23 | ||
| US11730599P | 1999-01-26 | 1999-01-26 | |
| US117305P | 1999-01-26 | ||
| US12002499P | 1999-02-13 | 1999-02-13 | |
| US120024P | 1999-02-13 |
Publications (1)
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|---|---|
| ES2222004T3 true ES2222004T3 (es) | 2005-01-16 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES99104756T Expired - Lifetime ES2222004T3 (es) | 1998-03-11 | 1999-03-10 | Caucho de estireno-butadieno, de emulsion. |
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| US (2) | US6469104B1 (enExample) |
| EP (1) | EP0942042B1 (enExample) |
| JP (1) | JP2000017021A (enExample) |
| KR (1) | KR100597804B1 (enExample) |
| CN (1) | CN1230564A (enExample) |
| AT (1) | ATE269376T1 (enExample) |
| AU (1) | AU1862899A (enExample) |
| BR (1) | BR9915758A (enExample) |
| CA (1) | CA2265153A1 (enExample) |
| CO (1) | CO5060538A1 (enExample) |
| DE (1) | DE69917959T2 (enExample) |
| ES (1) | ES2222004T3 (enExample) |
| HU (1) | HUP9900785A3 (enExample) |
| ID (1) | ID22093A (enExample) |
| NZ (1) | NZ334587A (enExample) |
| PE (1) | PE20000344A1 (enExample) |
| SG (1) | SG165133A1 (enExample) |
| SK (1) | SK31299A3 (enExample) |
| TR (1) | TR199900530A2 (enExample) |
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030050370A1 (en) | 2001-03-16 | 2003-03-13 | Victor Thielen Georges Marcel | Silica filled multi-viscoelastic response rubber |
| DE19963781A1 (de) * | 1998-12-31 | 2000-07-06 | Goodyear Tire & Rubber | Reifenlaufflächen-Compound |
| CA2301788A1 (en) * | 1999-05-12 | 2000-11-12 | The Goodyear Tire & Rubber Company | Endless rubber track and vehicle containing such track |
| CA2368002A1 (fr) * | 2000-02-02 | 2001-08-09 | Michelin Recherche Et Technique S.A. | Bande de roulement de pneumatique comprenant un copolymere styrene/butadiene prepare en emulsion |
| CA2368003A1 (fr) * | 2000-02-02 | 2001-08-09 | Roland Rauline | Bande de roulement de pneumatique comprenant un copolymere styrene/butadiene prepare en emulsion |
| DE60118364T8 (de) * | 2000-06-07 | 2007-05-10 | Zeon Corp. | Konjugiertes dienkautschukgel, kautschukzusammensetzungen die dieses enthalten und verfahren zur herstellung von konjugiertem dienkautschuk |
| US6455655B1 (en) * | 2000-09-28 | 2002-09-24 | The Goodyear Tire & Rubber Company | Emulsion styrene-butadiene rubber |
| EP1385708B1 (en) * | 2001-04-13 | 2004-10-13 | PIRELLI PNEUMATICI Società per Azioni | Tyre with high roadholding, tread band and elastomeric composition used therein |
| US8800615B2 (en) | 2005-03-14 | 2014-08-12 | Bridgestone Corporation | Rubber composition and pneumatic tire using the same |
| US20060266454A1 (en) * | 2005-05-27 | 2006-11-30 | Sandstrom Paul H | Tire with tread comprised of natural rubber and specialized emulsion prepared styrene/butadiene elastomer |
| EP1887037A1 (en) * | 2006-08-10 | 2008-02-13 | PolymerLatex GmbH | Latex with reduced odour |
| BRPI0603376A (pt) * | 2006-08-17 | 2008-04-08 | Petroflex Ind E Com S A | processo para a obtenção de copolìmeros de butadieno e estireno, através da polimerização em emulsão, agente modificador da reologia do copolìmero, composição de borracha, goma base, goma de mascar e goma para chicle de bola |
| US8136562B2 (en) * | 2006-12-29 | 2012-03-20 | Bridgestone Firestone North American Tire, Llc | Tire bead insulation |
| US7594528B2 (en) | 2007-03-08 | 2009-09-29 | The Goodyear Tire & Rubber Company | Tire with sidewall comprised of emulsion styrene/butadiene rubber, cis 1,4-polyisoprene rubber and cis 1,4-polybutadiene rubber |
| JP5259332B2 (ja) * | 2007-10-25 | 2013-08-07 | 東洋ゴム工業株式会社 | 空気入りタイヤ |
| JP5259337B2 (ja) * | 2007-11-19 | 2013-08-07 | 東洋ゴム工業株式会社 | 空気入りタイヤ |
| WO2010078248A2 (en) | 2008-12-31 | 2010-07-08 | Bridgestone Corporation | Rubber compositions including a polymeric component having a multi-modal molecular weight distribution |
| DE102010061469A1 (de) * | 2010-12-22 | 2012-06-28 | Continental Reifen Deutschland Gmbh | Kautschukmischung mit verbessertem Rollwiderstandsverhalten |
| RU2571135C2 (ru) * | 2011-06-03 | 2015-12-20 | Бриджстоун Корпорейшн | Резиновая смесь и шина, изготовляемая с ее использованием |
| NL2007262C2 (en) | 2011-08-12 | 2013-02-13 | Kraton Polymers Us Llc | A process for preparing articles from a latex comprising water and a styrenic block copolymer and such a latex. |
| EP2771397A4 (en) | 2011-10-24 | 2015-06-10 | Bridgestone Americas Tire | SILICA-CHARGED RUBBER COMPOSITION AND METHOD FOR MANUFACTURING THE SAME |
| CN102585316B (zh) * | 2012-04-20 | 2013-12-25 | 贵州轮胎股份有限公司 | 耐切割斜交轮胎胎面胶料及其制备方法 |
| JP6061919B2 (ja) * | 2012-05-09 | 2017-01-18 | 株式会社ブリヂストン | 天然ゴム、天然ゴムを含むゴム組成物及びその製造方法、及びタイヤ |
| CN103421144B (zh) * | 2012-05-16 | 2016-03-30 | 中国石油化工股份有限公司 | 一种母炼胶及其制备方法和硫化橡胶及其应用 |
| CN103450396B (zh) * | 2012-06-01 | 2015-05-27 | 中国石油天然气股份有限公司 | 一种乳液聚合法制备易加工型丁苯橡胶的方法 |
| US20140256858A1 (en) | 2013-03-11 | 2014-09-11 | Robert Anthony Bethea | Solution polymerization prepared styrene/butadiene elastomer containing liquid styrene/butadiene polymer and tire with component |
| CN104693455B (zh) * | 2015-02-15 | 2017-10-10 | 北京化工大学 | 一种溶聚丁苯橡胶乳液的制备方法 |
| KR101950705B1 (ko) | 2015-11-30 | 2019-02-21 | 주식회사 엘지화학 | 결합 스티렌 함량이 낮은 스티렌-부타디엔 고무의 제조방법 |
| CN107849195B (zh) | 2015-12-28 | 2020-10-23 | 株式会社Lg化学 | 丁苯橡胶的制备方法和丁苯橡胶 |
| CN105838879B (zh) * | 2016-03-29 | 2019-02-12 | 云南华联锌铟股份有限公司 | 从锌冶炼的沉铟后液中去除钙镁的方法和装置 |
| KR101950707B1 (ko) | 2016-11-10 | 2019-02-21 | 주식회사 엘지화학 | 스티렌-부타디엔 고무 컴파운드 및 이를 포함하는 타이어 비드 필러용 고무 조성물 |
| US10427463B2 (en) | 2016-11-16 | 2019-10-01 | The Goodyear Tire & Rubber Company | Pneumatic tire having a dual layer tread |
| CN106519119B (zh) * | 2016-11-30 | 2019-10-11 | 黄河三角洲京博化工研究院有限公司 | 一种丁苯胶乳的制备方法 |
| CN106519118A (zh) * | 2016-11-30 | 2017-03-22 | 黄河三角洲京博化工研究院有限公司 | 一种改性乳化沥青用丁苯胶乳的制备方法 |
| JP6922391B2 (ja) * | 2017-05-01 | 2021-08-18 | 住友ゴム工業株式会社 | タイヤ用ゴム組成物及び空気入りタイヤ |
| CN109776726B (zh) * | 2017-11-15 | 2021-11-02 | 中国石油天然气股份有限公司 | 丁苯橡胶的制备方法及丁苯橡胶 |
| WO2019133365A1 (en) * | 2017-12-26 | 2019-07-04 | Bridgestone Corporation | Synthesis of low molecular weight tapered styrene-butadiene copolymer and its use in tires |
| KR102648095B1 (ko) * | 2019-05-20 | 2024-03-18 | 주식회사 엘지화학 | 방사원액의 응고현상 분석방법 |
| EP4015238A1 (en) * | 2020-12-18 | 2022-06-22 | The Goodyear Tire & Rubber Company | Rubber composition, tire comprising such a rubber composition and its method of manufacturing |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4110240A (en) * | 1977-07-29 | 1978-08-29 | Wyrough And Loser, Inc. | Coprecipitation process |
| CA1196139A (en) * | 1982-02-26 | 1985-10-29 | Hiroshi Furukawa | Elastomer composition |
| JPS60192739A (ja) * | 1984-03-15 | 1985-10-01 | Japan Synthetic Rubber Co Ltd | ブロック共重合体 |
| JPH0637578B2 (ja) * | 1988-02-01 | 1994-05-18 | 日本合成ゴム株式会社 | ゴム組成物 |
| US5202387A (en) | 1992-05-08 | 1993-04-13 | The Goodyear Tire & Rubber Company | Elastomer with outstanding characteristics for use in making tire tread compounds |
| JP3290469B2 (ja) * | 1992-08-17 | 2002-06-10 | ジェイエスアール株式会社 | ゴム組成物 |
| JPH07188462A (ja) * | 1993-12-27 | 1995-07-25 | Bridgestone Corp | タイヤトレッド用ゴム組成物 |
| US5583173A (en) * | 1995-04-10 | 1996-12-10 | The Goodyear Tire & Rubber Company | Process for preparing styrene-butadiene rubber |
| DE69612912T2 (de) * | 1995-06-30 | 2001-10-18 | Bridgestone Corp., Tokio/Tokyo | Kautschukmischung und daraus hergestellter Reifen |
| US5837756A (en) | 1997-05-28 | 1998-11-17 | The Goodyear Tire & Rubber Company | Polymer for asphalt cement modification |
| US6136899A (en) * | 1999-09-14 | 2000-10-24 | The Goodyear Tire & Rubber Company | SBR for asphalt cement modification |
-
1999
- 1999-03-08 SG SG9901075-3A patent/SG165133A1/en unknown
- 1999-03-08 AU AU18628/99A patent/AU1862899A/en not_active Abandoned
- 1999-03-09 SK SK312-99A patent/SK31299A3/sk unknown
- 1999-03-09 US US09/264,937 patent/US6469104B1/en not_active Expired - Fee Related
- 1999-03-10 NZ NZ334587A patent/NZ334587A/en unknown
- 1999-03-10 ES ES99104756T patent/ES2222004T3/es not_active Expired - Lifetime
- 1999-03-10 EP EP99104756A patent/EP0942042B1/en not_active Expired - Lifetime
- 1999-03-10 CO CO99014708A patent/CO5060538A1/es unknown
- 1999-03-10 ID IDP990204D patent/ID22093A/id unknown
- 1999-03-10 CA CA002265153A patent/CA2265153A1/en not_active Abandoned
- 1999-03-10 AT AT99104756T patent/ATE269376T1/de not_active IP Right Cessation
- 1999-03-10 BR BR9915758-6A patent/BR9915758A/pt not_active Application Discontinuation
- 1999-03-10 DE DE69917959T patent/DE69917959T2/de not_active Expired - Fee Related
- 1999-03-10 KR KR1019990007948A patent/KR100597804B1/ko not_active Expired - Fee Related
- 1999-03-11 JP JP11064663A patent/JP2000017021A/ja not_active Withdrawn
- 1999-03-11 TR TR1999/00530A patent/TR199900530A2/xx unknown
- 1999-03-11 PE PE1999000194A patent/PE20000344A1/es not_active Application Discontinuation
- 1999-03-11 CN CN99105530A patent/CN1230564A/zh active Pending
- 1999-03-26 HU HU9900785A patent/HUP9900785A3/hu unknown
-
2000
- 2000-10-17 US US09/690,555 patent/US6458884B1/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EP0942042B1 (en) | 2004-06-16 |
| AU1862899A (en) | 1999-09-23 |
| SG165133A1 (en) | 2010-10-28 |
| BR9915758A (pt) | 2001-07-24 |
| HUP9900785A2 (hu) | 1999-08-30 |
| KR100597804B1 (ko) | 2006-07-10 |
| SK31299A3 (en) | 2000-10-09 |
| HUP9900785A3 (en) | 1999-11-29 |
| PE20000344A1 (es) | 2000-04-20 |
| DE69917959D1 (de) | 2004-07-22 |
| NZ334587A (en) | 2000-06-23 |
| TR199900530A2 (xx) | 1999-10-21 |
| JP2000017021A (ja) | 2000-01-18 |
| ID22093A (id) | 1999-09-02 |
| KR19990077755A (ko) | 1999-10-25 |
| US6469104B1 (en) | 2002-10-22 |
| CA2265153A1 (en) | 1999-09-11 |
| US6458884B1 (en) | 2002-10-01 |
| HU9900785D0 (en) | 1999-05-28 |
| ATE269376T1 (de) | 2004-07-15 |
| EP0942042A3 (en) | 2001-11-07 |
| DE69917959T2 (de) | 2005-06-30 |
| CN1230564A (zh) | 1999-10-06 |
| EP0942042A2 (en) | 1999-09-15 |
| CO5060538A1 (es) | 2001-07-30 |
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