JP6540960B2 - ポリカルボン酸で架橋したエポキシドエラストマーを含むゴム組成物を含有するタイヤ - Google Patents
ポリカルボン酸で架橋したエポキシドエラストマーを含むゴム組成物を含有するタイヤ Download PDFInfo
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- JP6540960B2 JP6540960B2 JP2015547029A JP2015547029A JP6540960B2 JP 6540960 B2 JP6540960 B2 JP 6540960B2 JP 2015547029 A JP2015547029 A JP 2015547029A JP 2015547029 A JP2015547029 A JP 2015547029A JP 6540960 B2 JP6540960 B2 JP 6540960B2
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- 239000000203 mixture Substances 0.000 title claims description 119
- 229920001971 elastomer Polymers 0.000 title claims description 76
- 239000005060 rubber Substances 0.000 title claims description 43
- 239000002253 acid Substances 0.000 title claims description 15
- 239000000806 elastomer Substances 0.000 title description 33
- 150000002118 epoxides Chemical class 0.000 title 1
- 125000004432 carbon atom Chemical group C* 0.000 claims description 70
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 64
- 229920003244 diene elastomer Polymers 0.000 claims description 48
- 125000003118 aryl group Chemical group 0.000 claims description 28
- 239000012763 reinforcing filler Substances 0.000 claims description 25
- 125000000217 alkyl group Chemical group 0.000 claims description 24
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 24
- 238000004132 cross linking Methods 0.000 claims description 17
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- 125000005842 heteroatom Chemical group 0.000 claims description 13
- 244000043261 Hevea brasiliensis Species 0.000 claims description 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 12
- 229920003052 natural elastomer Polymers 0.000 claims description 12
- 229920001194 natural rubber Polymers 0.000 claims description 12
- 125000002883 imidazolyl group Chemical group 0.000 claims description 8
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- TVIDDXQYHWJXFK-UHFFFAOYSA-N dodecanedioic acid Chemical compound OC(=O)CCCCCCCCCCC(O)=O TVIDDXQYHWJXFK-UHFFFAOYSA-N 0.000 claims description 3
- 125000001072 heteroaryl group Chemical group 0.000 claims description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 3
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 47
- 239000000377 silicon dioxide Substances 0.000 description 21
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 21
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- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 16
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
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- FBHPRUXJQNWTEW-UHFFFAOYSA-N 1-benzyl-2-methylimidazole Chemical compound CC1=NC=CN1CC1=CC=CC=C1 FBHPRUXJQNWTEW-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 3
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
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- QFGCFKJIPBRJGM-UHFFFAOYSA-N 12-[(2-methylpropan-2-yl)oxy]-12-oxododecanoic acid Chemical compound CC(C)(C)OC(=O)CCCCCCCCCCC(O)=O QFGCFKJIPBRJGM-UHFFFAOYSA-N 0.000 description 2
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- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
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- 239000012190 activator Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- QMKYBPDZANOJGF-UHFFFAOYSA-N benzene-1,3,5-tricarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(C(O)=O)=C1 QMKYBPDZANOJGF-UHFFFAOYSA-N 0.000 description 2
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- 125000002897 diene group Chemical group 0.000 description 2
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- DEQZTKGFXNUBJL-UHFFFAOYSA-N n-(1,3-benzothiazol-2-ylsulfanyl)cyclohexanamine Chemical compound C1CCCCC1NSC1=NC2=CC=CC=C2S1 DEQZTKGFXNUBJL-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
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- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 150000004756 silanes Chemical class 0.000 description 2
- 230000000930 thermomechanical effect Effects 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 125000006832 (C1-C10) alkylene group Chemical group 0.000 description 1
- GIWQSPITLQVMSG-UHFFFAOYSA-N 1,2-dimethylimidazole Chemical compound CC1=NC=CN1C GIWQSPITLQVMSG-UHFFFAOYSA-N 0.000 description 1
- BKFRZOZNMWIFLH-UHFFFAOYSA-N 1-decyl-2-methylimidazole Chemical compound CCCCCCCCCCN1C=CN=C1C BKFRZOZNMWIFLH-UHFFFAOYSA-N 0.000 description 1
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- ZZMVLMVFYMGSMY-UHFFFAOYSA-N 4-n-(4-methylpentan-2-yl)-1-n-phenylbenzene-1,4-diamine Chemical compound C1=CC(NC(C)CC(C)C)=CC=C1NC1=CC=CC=C1 ZZMVLMVFYMGSMY-UHFFFAOYSA-N 0.000 description 1
- KZTCAXCBXSIQSS-UHFFFAOYSA-N 4-n-(4-methylpentan-2-yl)-4-n-phenylbenzene-1,4-diamine Chemical compound C=1C=C(N)C=CC=1N(C(C)CC(C)C)C1=CC=CC=C1 KZTCAXCBXSIQSS-UHFFFAOYSA-N 0.000 description 1
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- DCXXMTOCNZCJGO-UHFFFAOYSA-N Glycerol trioctadecanoate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 1
- 239000013032 Hydrocarbon resin Substances 0.000 description 1
- 239000006237 Intermediate SAF Substances 0.000 description 1
- 239000004594 Masterbatch (MB) Substances 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- SCPNGMKCUAZZOO-UHFFFAOYSA-N [3-[(3-dimethylsilyl-3-ethoxypropyl)tetrasulfanyl]-1-ethoxypropyl]-dimethylsilane Chemical class CCOC([SiH](C)C)CCSSSSCCC([SiH](C)C)OCC SCPNGMKCUAZZOO-UHFFFAOYSA-N 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
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- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
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- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
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- XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical compound CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 description 1
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- 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
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- GKIPXFAANLTWBM-UHFFFAOYSA-N epibromohydrin Chemical compound BrCC1CO1 GKIPXFAANLTWBM-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
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- 230000005484 gravity Effects 0.000 description 1
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 description 1
- 239000011325 microbead Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- MSRJTTSHWYDFIU-UHFFFAOYSA-N octyltriethoxysilane Chemical compound CCCCCCCC[Si](OCC)(OCC)OCC MSRJTTSHWYDFIU-UHFFFAOYSA-N 0.000 description 1
- 150000001282 organosilanes Chemical class 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- KHIWWQKSHDUIBK-UHFFFAOYSA-N periodic acid Chemical compound OI(=O)(=O)=O KHIWWQKSHDUIBK-UHFFFAOYSA-N 0.000 description 1
- 150000004965 peroxy acids Chemical class 0.000 description 1
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- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 150000003141 primary amines Chemical class 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
- 230000009467 reduction Effects 0.000 description 1
- 239000006235 reinforcing carbon black Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- FBBATURSCRIBHN-UHFFFAOYSA-N triethoxy-[3-(3-triethoxysilylpropyldisulfanyl)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCSSCCC[Si](OCC)(OCC)OCC FBBATURSCRIBHN-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
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
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
- C08K3/34—Silicon-containing compounds
- C08K3/36—Silica
-
- 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
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/092—Polycarboxylic acids
-
- 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
-
- 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
- C08K3/02—Elements
- C08K3/04—Carbon
-
- 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
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3442—Heterocyclic compounds having nitrogen in the ring having two nitrogen atoms in the ring
- C08K5/3445—Five-membered rings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L15/00—Compositions of rubber derivatives
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)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR1262162 | 2012-12-17 | ||
| FR1262162A FR2999587B1 (fr) | 2012-12-17 | 2012-12-17 | Pneumatique comportant une composition de caoutchouc comprenant un elastomere epoxyde reticule par un poly-acide carboxylique |
| PCT/EP2013/076417 WO2014095583A1 (fr) | 2012-12-17 | 2013-12-12 | Pneumatique comportant une composition de caoutchouc comprenant un elastomere epoxyde reticule par un poly-acide carboxylique |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016501940A JP2016501940A (ja) | 2016-01-21 |
| JP2016501940A5 JP2016501940A5 (enExample) | 2017-01-26 |
| JP6540960B2 true JP6540960B2 (ja) | 2019-07-10 |
Family
ID=47833276
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015547029A Expired - Fee Related JP6540960B2 (ja) | 2012-12-17 | 2013-12-12 | ポリカルボン酸で架橋したエポキシドエラストマーを含むゴム組成物を含有するタイヤ |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20150337109A1 (enExample) |
| EP (1) | EP2931529B1 (enExample) |
| JP (1) | JP6540960B2 (enExample) |
| CN (1) | CN104870206B (enExample) |
| FR (1) | FR2999587B1 (enExample) |
| WO (1) | WO2014095583A1 (enExample) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2999588B1 (fr) * | 2012-12-17 | 2015-02-13 | Michelin & Cie | Pneumatique comportant une composition de caoutchouc comprenant un elastomere epoxyde reticule par un poly-acide carboxylique |
| FR3006320B1 (fr) * | 2013-05-28 | 2015-05-29 | Michelin & Cie | Pneumatique comportant une composition de caoutchouc comprenant un elastomere olefinique epoxyde reticule par un poly-acide carboxylique |
| FR3022547B1 (fr) * | 2014-06-18 | 2016-06-24 | Michelin & Cie | Procede de preparation d'une composition de caoutchouc comprenant un elastomere epoxyde reticule par un poly-acide carboxylique |
| FR3022548A1 (fr) * | 2014-06-18 | 2015-12-25 | Michelin & Cie | Composition de caoutchouc comprenant un elastomere epoxyde reticule par un poly-acide carboxylique |
| JP6869163B2 (ja) * | 2017-10-20 | 2021-05-12 | 株式会社ブリヂストン | ゴム組成物 |
| JP7275136B2 (ja) * | 2017-12-21 | 2023-05-17 | コンパニー ゼネラール デ エタブリッスマン ミシュラン | フェノール化合物を含む二酸架橋ゴム組成物 |
| CN110642964B (zh) * | 2018-06-27 | 2020-10-27 | 北京化工大学 | 一种可重复加工的环氧官能化橡胶交联弹性体及制备方法 |
| FR3089990A3 (fr) * | 2018-12-17 | 2020-06-19 | Michelin & Cie | Composition de caoutchouc à base d’au moins un élastomère fonctionnalisé comprenant des groupes fonctionnels polaires et un composé polyphénolique spécifique |
| FR3097224B1 (fr) * | 2019-06-11 | 2021-05-21 | Michelin & Cie | Polymère greffé portant des groupes pendants fonctionnels imidazole. |
| FR3101877B1 (fr) | 2019-10-10 | 2022-06-17 | Michelin & Cie | Composition de caoutchouc comprenant un élastomère diénique comprenant des fonctions carbonates |
| FR3101878B1 (fr) | 2019-10-10 | 2021-10-01 | Michelin & Cie | Compositions de caoutchouc comprenant un élastomère diénique époxydé et un système de réticulation |
| FR3104590B1 (fr) | 2019-12-12 | 2021-12-03 | Michelin & Cie | Composite comprenant un élément de renfort et une composition de caoutchouc |
| FR3104593B1 (fr) | 2019-12-12 | 2021-12-03 | Michelin & Cie | Système de réticulation et composition de caoutchouc diénique le comprenant |
| FR3104592B1 (fr) | 2019-12-12 | 2021-12-03 | Michelin & Cie | Système de réticulation et composition de caoutchouc diénique le comprenant |
| JP7552022B2 (ja) * | 2020-02-05 | 2024-09-18 | 住友ゴム工業株式会社 | ゴム組成物及びタイヤ |
| FR3122658B1 (fr) * | 2021-05-10 | 2024-06-14 | Michelin & Cie | Composite à base d’une composition de caoutchouc et d’un élément de renfort métallique traité au plasma |
| FR3122657B1 (fr) * | 2021-05-10 | 2024-06-21 | Michelin & Cie | Composite à base d’une composition de caoutchouc et d’un élément de renfort métallique traité en milieu supercritique |
| JP2023174336A (ja) * | 2022-05-27 | 2023-12-07 | 住友ゴム工業株式会社 | タイヤ用ゴム組成物およびタイヤ |
Family Cites Families (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2731481A (en) * | 1951-08-01 | 1956-01-17 | Gen Mills Inc | Dimeric fatty acids |
| US3843466A (en) | 1969-11-10 | 1974-10-22 | Ajinomoto Kk | Method of producing dicarboxylic acids by fermentation |
| JPS61171727A (ja) * | 1985-01-28 | 1986-08-02 | Dainippon Ink & Chem Inc | 新設または修繕用エポキシ樹脂組成物およびそれを含んだ施工材料 |
| IT1245551B (it) * | 1991-05-17 | 1994-09-29 | Firestone Int Dev Spa | Procedimento per la vulcanizzazione senza zolfo di un elastomero e mescole autovulcanizzanti a base di elastomeri epossidati. |
| JPH07304902A (ja) * | 1994-05-09 | 1995-11-21 | Daicel Chem Ind Ltd | 天然ゴム系組成物 |
| IT1277581B1 (it) | 1995-09-14 | 1997-11-11 | Enichem Elastomers | Composizione elastomerica utile come battistrada per pneumatici |
| CN101186724B (zh) | 1996-04-01 | 2011-01-19 | 卡伯特公司 | 新型弹性体组合物、其制备方法及设备 |
| KR100617997B1 (ko) | 1997-09-30 | 2006-09-05 | 캐보트 코포레이션 | 엘라스토머 복합재 블렌드 및 그들의 제조 방법 |
| BR9916543B1 (pt) * | 1998-12-22 | 2008-11-18 | processo para a produÇço de pneus para as rodas de veÍculos, composiÇço compreendendo um polÍmero elastomÉrico, processo para a preparaÇço de uma composiÇço elastomÉrica, produto reticulado manufaturado, e, pneu para rodas de veÍculos. | |
| US20060231183A1 (en) * | 2000-06-14 | 2006-10-19 | Antonio Serra | Process for producing tyres, tyres thus obtained and elastomeric compositions used therein |
| JP2004521772A (ja) * | 2000-06-14 | 2004-07-22 | ピレリ・プネウマティチ・ソチエタ・ペル・アツィオーニ | タイヤを製造する方法、それにより得られるタイヤ、およびそこに用いられるエラストマー組成物 |
| CN1263792C (zh) | 2000-10-13 | 2006-07-12 | 米其林技术公司 | 包含多官能有机硅烷作为偶联剂的橡胶组合物 |
| ES2256317T3 (es) | 2000-10-13 | 2006-07-16 | Societe De Technologie Michelin | Organosilano polifuncional utilizable como agente de acoplamiento y su procedimiento de obtencion. |
| FR2823215B1 (fr) | 2001-04-10 | 2005-04-08 | Michelin Soc Tech | Pneumatique et bande de roulement de pneumatique comportant a titre d'agent de couplage un tetrasulfure de bis-alkoxysilane |
| EP1403287B1 (en) | 2001-05-14 | 2010-01-06 | DAICEL CHEMICAL INDUSTRIES, Ltd. | Process for producing epoxidized diene polymer |
| CN1325549C (zh) | 2001-06-28 | 2007-07-11 | 米其林技术公司 | 采用具有非常低比表面积的二氧化硅增强的轮胎胎面 |
| WO2003002648A1 (fr) | 2001-06-28 | 2003-01-09 | Societe De Technologie Michelin | Bande de roulement pour pneumatique renforcee d'une silice a basse surface specifique |
| SE519792C2 (sv) | 2001-08-17 | 2003-04-08 | Volvo Lastvagnar Ab | Metod för estimering av massan hos ett fordon vilket framförs på en väg med en varierande lutning samt metod för estimering av lutningen av den väg där ett fordon framförs |
| US6845797B2 (en) * | 2001-10-12 | 2005-01-25 | Bridgestone Corporation | Tire compositions comprising epoxidized natural rubber and a functionalized polyolefin |
| JP2003238735A (ja) * | 2002-02-15 | 2003-08-27 | Bridgestone Corp | ゴム組成物及びそれを用いた空気入りタイヤ |
| DE602004001807T2 (de) * | 2003-06-03 | 2007-08-02 | Sumitomo Rubber Industries Ltd., Kobe | Gummizusammensetzung für Reifenlaufflächen und peneumatischer Reifen auf der Basis derselben |
| US7836928B2 (en) * | 2004-10-26 | 2010-11-23 | Bridgestone Corporation | Method of producing a tire composition having improved silica reinforcement |
| FR2880354B1 (fr) | 2004-12-31 | 2007-03-02 | Michelin Soc Tech | Composition elastomerique renforcee d'une charge de polyvinylaromatique fonctionnalise |
| FR2880349B1 (fr) | 2004-12-31 | 2009-03-06 | Michelin Soc Tech | Nanoparticules de polyvinylaromatique fonctionnalise |
| FR2886305B1 (fr) | 2005-05-26 | 2007-08-10 | Michelin Soc Tech | Composition de caoutchouc pour pneumatique comportant un agent de couplage organosilicique et un agent de recouvrement de charge inorganique |
| FR2886304B1 (fr) | 2005-05-26 | 2007-08-10 | Michelin Soc Tech | Composition de caoutchouc pour pneumatique comportant un systeme de couplage organosilicique |
| FR2886306B1 (fr) | 2005-05-26 | 2007-07-06 | Michelin Soc Tech | Composition de caoutchouc pour pneumatique comportant un agent de couplage organosiloxane |
| ATE474727T1 (de) * | 2006-03-03 | 2010-08-15 | Pirelli | Reifen aus einer vernetzten elastomeren zusammensetzung |
| JP5005940B2 (ja) | 2006-03-30 | 2012-08-22 | 日本合成化学工業株式会社 | ジアルキルイミダゾールの製造方法 |
| US7534917B1 (en) | 2006-04-27 | 2009-05-19 | The United States Of America As Represented By The Secretary Of Agriculture | Method of producing dicarboxylic acids |
| FR2903411B1 (fr) | 2006-07-06 | 2012-11-02 | Soc Tech Michelin | Nanoparticules de polymere vinylique fonctionnalise |
| FR2903416B1 (fr) | 2006-07-06 | 2008-09-05 | Michelin Soc Tech | Composition elastomerique renforcee d'une charge de polymere vinylique non aromatique fonctionnalise |
| BRPI0622192B1 (pt) * | 2006-12-13 | 2019-11-19 | Pirelli | pneu |
| JP2010180337A (ja) * | 2009-02-06 | 2010-08-19 | Nippon Soda Co Ltd | 半導体封止用エポキシ樹脂組成物 |
| JP4821868B2 (ja) * | 2009-03-13 | 2011-11-24 | 横浜ゴム株式会社 | 熱可塑性エラストマー組成物 |
| FR2943680B1 (fr) * | 2009-03-31 | 2012-12-28 | Michelin Soc Tech | Composition de caoutchoux et pneumatique utilisant cette composition. |
| FR2946050B1 (fr) * | 2009-06-02 | 2016-10-28 | Rhodia Operations | Utilisation comme agent de couplage,dans une composition d'elastomere(s)comprenant une charge inorganique renforcante d'un compose organosilicique fonctionnalise particulier |
| JP5518501B2 (ja) * | 2010-01-21 | 2014-06-11 | 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 |
| JP5249404B2 (ja) * | 2010-12-13 | 2013-07-31 | 住友ゴム工業株式会社 | ゴム組成物及び空気入りタイヤ |
| JP2012211122A (ja) | 2011-03-22 | 2012-11-01 | Nippon Synthetic Chem Ind Co Ltd:The | 1,2−ジアルキルイミダゾールの製造方法、および1,2−ジアルキルイミダゾール |
| JP5438169B2 (ja) * | 2012-06-21 | 2014-03-12 | 住友ゴム工業株式会社 | ゴム組成物およびそれを用いたタイヤ |
| FR2999588B1 (fr) * | 2012-12-17 | 2015-02-13 | Michelin & Cie | Pneumatique comportant une composition de caoutchouc comprenant un elastomere epoxyde reticule par un poly-acide carboxylique |
| FR2999589B1 (fr) * | 2012-12-17 | 2014-12-26 | Michelin & Cie | Pneumatique comportant une composition de caoutchouc comprenant un elastomere epoxyde reticule par un poly-acide carboxylique |
-
2012
- 2012-12-17 FR FR1262162A patent/FR2999587B1/fr not_active Expired - Fee Related
-
2013
- 2013-12-12 JP JP2015547029A patent/JP6540960B2/ja not_active Expired - Fee Related
- 2013-12-12 US US14/652,899 patent/US20150337109A1/en not_active Abandoned
- 2013-12-12 CN CN201380065999.1A patent/CN104870206B/zh not_active Expired - Fee Related
- 2013-12-12 EP EP13803025.9A patent/EP2931529B1/fr not_active Not-in-force
- 2013-12-12 WO PCT/EP2013/076417 patent/WO2014095583A1/fr not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| FR2999587B1 (fr) | 2014-12-26 |
| FR2999587A1 (fr) | 2014-06-20 |
| JP2016501940A (ja) | 2016-01-21 |
| WO2014095583A1 (fr) | 2014-06-26 |
| US20150337109A1 (en) | 2015-11-26 |
| EP2931529A1 (fr) | 2015-10-21 |
| CN104870206B (zh) | 2017-11-24 |
| CN104870206A (zh) | 2015-08-26 |
| EP2931529B1 (fr) | 2018-02-21 |
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