DE60101001T2 - Kautschukzusammensetzung für reifen, die einen anorganischen verstärkenden füllstoff und ein kupplungssystem (anorganischer füllstoff/elastomer) enthält - Google Patents
Kautschukzusammensetzung für reifen, die einen anorganischen verstärkenden füllstoff und ein kupplungssystem (anorganischer füllstoff/elastomer) enthält Download PDFInfo
- Publication number
- DE60101001T2 DE60101001T2 DE60101001T DE60101001T DE60101001T2 DE 60101001 T2 DE60101001 T2 DE 60101001T2 DE 60101001 T DE60101001 T DE 60101001T DE 60101001 T DE60101001 T DE 60101001T DE 60101001 T2 DE60101001 T2 DE 60101001T2
- Authority
- DE
- Germany
- Prior art keywords
- aldimine
- inorganic filler
- asps
- filler
- reinforcing
- 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
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- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 238000000386 microscopy Methods 0.000 description 1
- 239000004005 microsphere Substances 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 230000006855 networking Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl 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])[H] 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- SOQBVABWOPYFQZ-UHFFFAOYSA-N oxygen(2-);titanium(4+) Chemical class [O-2].[O-2].[Ti+4] SOQBVABWOPYFQZ-UHFFFAOYSA-N 0.000 description 1
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N pentanal Chemical compound CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920003192 poly(bis maleimide) Polymers 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001223 polyethylene glycol 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
- 238000002360 preparation method Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 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
- 239000003223 protective agent Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 125000005372 silanol group Chemical group 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229920006027 ternary co-polymer Polymers 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 229920003194 trans-1,4-polybutadiene polymer Polymers 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 239000012936 vulcanization activator Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 125000005023 xylyl group Chemical group 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
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/29—Compounds containing one or more carbon-to-nitrogen double bonds
-
- 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
- C08K5/54—Silicon-containing compounds
- C08K5/5406—Silicon-containing compounds containing elements other than oxygen or nitrogen
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0001012A FR2804120A1 (fr) | 2000-01-24 | 2000-01-24 | Composition de caoutchouc pour pneumatique comportant une charge blanche renforcante et un systeme de couplage (charge blanche/elstomere) |
| FR0001012 | 2000-01-24 | ||
| PCT/EP2001/000662 WO2001055253A1 (fr) | 2000-01-24 | 2001-01-22 | Composition de caoutchouc pour pneumatique comportant une charge inorganique renforçante et un systeme de couplage (charge inorganique/elastomere) |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE60101001D1 DE60101001D1 (de) | 2003-11-20 |
| DE60101001T2 true DE60101001T2 (de) | 2004-07-15 |
Family
ID=8846345
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE60101001T Expired - Lifetime DE60101001T2 (de) | 2000-01-24 | 2001-01-22 | Kautschukzusammensetzung für reifen, die einen anorganischen verstärkenden füllstoff und ein kupplungssystem (anorganischer füllstoff/elastomer) enthält |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US6951897B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP1268650B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP5033289B2 (cg-RX-API-DMAC7.html) |
| CN (1) | CN1239592C (cg-RX-API-DMAC7.html) |
| AT (1) | ATE252129T1 (cg-RX-API-DMAC7.html) |
| AU (1) | AU2001230203A1 (cg-RX-API-DMAC7.html) |
| DE (1) | DE60101001T2 (cg-RX-API-DMAC7.html) |
| FR (1) | FR2804120A1 (cg-RX-API-DMAC7.html) |
| WO (1) | WO2001055253A1 (cg-RX-API-DMAC7.html) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3150401A1 (de) | 2015-09-29 | 2017-04-05 | Continental Reifen Deutschland GmbH | Kautschukmischung und fahrzeugreifen |
| DE102016201195A1 (de) | 2016-01-27 | 2017-07-27 | Continental Reifen Deutschland Gmbh | Kautschukmischung und Fahrzeugreifen |
| DE102016225584A1 (de) | 2016-12-20 | 2018-06-21 | Continental Reifen Deutschland Gmbh | Schwefelvernetzbare Kautschukmischung, Vulkanisat der Kautschukmischung und Fahrzeugreifen |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2501390A1 (fr) * | 2002-10-11 | 2004-04-22 | Michelin Recherche Et Technique S.A. | Ceinture de pneumatique a base d'une charge inorganique et d'un silane-polysulfure |
| US7141622B2 (en) * | 2003-07-30 | 2006-11-28 | The Goodyear Tire & Rubber Company | Process for preparing a silica/rubber blend which includes dispersing silica, asilica coupling agent, and a low molecular weight end-group functionalized diene rubber throughout a cement of a conventional rubbery polymer, and subsequently recovering the silica/rubber blend from an organic solvent |
| US7572851B2 (en) * | 2003-07-30 | 2009-08-11 | The Goodyear Tire & Rubber Company | Process for preparing a silica rubber blend |
| FR2886302B1 (fr) * | 2005-05-26 | 2007-06-29 | Rhodia Chimie Sa | Utilisation d'une combinaison de deux types d'agents de couplage bien differents, comme systeme de couplage (charge blanche-elastomere) dans les compositions de caoutchouc comprenant une charge inorganique |
| EP1885775B1 (en) * | 2005-05-26 | 2013-07-24 | Bridgestone Corporation | Enhancing interactivity between amine-functionalized polymers and particulate fillers |
| FR2903416B1 (fr) * | 2006-07-06 | 2008-09-05 | Michelin Soc Tech | Composition elastomerique renforcee d'une charge de polymere vinylique non aromatique fonctionnalise |
| US10023723B2 (en) * | 2007-06-05 | 2018-07-17 | Momentive Performance Materials Inc. | Process for preparing rubber compositions and articles made therefrom |
| BRPI0821878A2 (pt) | 2008-01-04 | 2019-09-10 | Bard Inc C R | composições, métodos de cura de látex de poliisopreno sintético e cateter de drenagem urinária não residente |
| WO2010002914A1 (en) | 2008-06-30 | 2010-01-07 | C.R. Bard, Inc. | Polyurethane/polysoprene blend catheter |
| TWI398368B (zh) * | 2010-01-29 | 2013-06-11 | Kenda Industry Co Ltd | Tire-free tire |
| US9228072B2 (en) | 2010-10-01 | 2016-01-05 | Bridgestone Corporation | Method for manufacturing rubber composition |
| CN103189424B (zh) | 2010-10-01 | 2014-12-31 | 株式会社普利司通 | 橡胶组合物的制造方法 |
| CN103189423B (zh) * | 2010-10-01 | 2014-12-31 | 株式会社普利司通 | 橡胶组合物的制造方法 |
| WO2012043855A1 (ja) * | 2010-10-01 | 2012-04-05 | 株式会社ブリヂストン | ゴム組成物の製造方法 |
| BR112013021475A2 (pt) | 2011-02-23 | 2016-10-11 | Bridgestone Corp | composição de borracha e pneu produzido utilizando-se a mesma e processo de produção de composição de borracha |
| WO2012137951A1 (ja) | 2011-04-06 | 2012-10-11 | 株式会社ブリヂストン | ゴム組成物の製造方法 |
| EP2703439A4 (en) | 2011-04-28 | 2015-06-10 | Bridgestone Corp | RUBBER COMPOSITION |
| JP5894588B2 (ja) | 2011-04-28 | 2016-03-30 | 株式会社ブリヂストン | ゴム組成物の製造方法 |
| WO2012147891A1 (ja) * | 2011-04-28 | 2012-11-01 | 株式会社ブリヂストン | ゴム組成物 |
| BR112013027610A2 (pt) | 2011-04-28 | 2017-02-14 | Bridgestone Corp | composição de borracha |
| BR112013027611A2 (pt) | 2011-04-28 | 2017-02-14 | Bridgestone Corp | método para fabricar uma composição de borracha |
| EP2703442B1 (en) | 2011-04-28 | 2016-04-27 | Bridgestone Corporation | Rubber composition |
| EP3502176A1 (en) | 2011-04-28 | 2019-06-26 | Bridgestone Corporation | Production method of a rubber composition |
| CN103635522B (zh) | 2011-04-28 | 2016-03-02 | 株式会社普利司通 | 橡胶组合物 |
| JP5783797B2 (ja) | 2011-05-25 | 2015-09-24 | 株式会社ブリヂストン | ゴム組成物の製造方法 |
| JP6328558B2 (ja) * | 2011-10-24 | 2018-05-23 | ブリヂストン アメリカズ タイヤ オペレイションズ エルエルシー | シリカ充填ゴム組成物及びその調整方法 |
| US20140296375A1 (en) * | 2011-10-24 | 2014-10-02 | Bridgestone Americas Tire Operations, Llc | Silica-Filled Rubber Composition And Method For Making The Same |
| JP5977517B2 (ja) | 2011-12-26 | 2016-08-24 | 株式会社ブリヂストン | ゴム組成物の製造方法、そのゴム組成物及びそれを用いた空気入りタイヤ |
| JP5838089B2 (ja) | 2011-12-26 | 2015-12-24 | 株式会社ブリヂストン | ゴム組成物の製造方法 |
| FR2986531B1 (fr) * | 2012-02-07 | 2014-02-28 | Michelin & Cie | Composition a base de caoutchouc naturel et d'un compose poly-aldimine |
| US10501601B2 (en) | 2013-05-31 | 2019-12-10 | Bridgestone Corporation | Tire rubber composition and manufacturing method therefor |
| CN116060214B (zh) * | 2022-12-21 | 2023-07-21 | 昆明理工大学 | 一种高钙硅质氧化锌矿的多金属耦合活化浮选方法 |
Family Cites Families (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1310379A (en) | 1970-12-10 | 1973-03-21 | Ppg Industries Inc | Tire tread |
| US3873489A (en) | 1971-08-17 | 1975-03-25 | Degussa | Rubber compositions containing silica and an organosilane |
| BE787691A (fr) | 1971-08-17 | 1973-02-19 | Degussa | Composes organosiliciques contenant du soufre |
| US3978103A (en) | 1971-08-17 | 1976-08-31 | Deutsche Gold- Und Silber-Scheideanstalt Vormals Roessler | Sulfur containing organosilicon compounds |
| BG25805A3 (en) | 1972-11-13 | 1978-12-12 | Degussa Ag | A rubber mixture |
| SU580840A3 (ru) | 1974-02-07 | 1977-11-15 | Дегусса (Фирма) | Способ получени серосодержащих кремнийорганических соединений |
| US4002594A (en) | 1975-07-08 | 1977-01-11 | Ppg Industries, Inc. | Scorch retardants for rubber reinforced with siliceous pigment and mercapto-type coupling agent |
| DE2542534C3 (de) | 1975-09-24 | 1979-08-02 | Deutsche Gold- Und Silber-Scheideanstalt Vormals Roessler, 6000 Frankfurt | Verfahren zur Herstellung von schwefelhaltigen Organosiliciumverbindungen |
| DE2712866C3 (de) | 1977-03-24 | 1980-04-30 | Deutsche Gold- Und Silber-Scheideanstalt Vormals Roessler, 6000 Frankfurt | Verfahren zum Herstellen von schwefelhaltigen Organosiliciumverbindungen |
| IE50442B1 (en) | 1980-11-21 | 1986-04-16 | Loctite Corp | Two part adhesive composition |
| WO1987004172A1 (fr) * | 1986-01-10 | 1987-07-16 | Asahi Kasei Kogyo Kabushiki Kaisha | Caoutchouc pour la bande de roulement de pneus |
| IT1233882B (it) | 1988-03-25 | 1992-04-21 | Mini Ricerca Scient Tecnolog | Composizioni adesive. |
| US5268413A (en) * | 1990-04-09 | 1993-12-07 | Bridgestone/Firestone, Inc. | Elastomers and products having reduced hysteresis |
| US5109907A (en) * | 1990-04-09 | 1992-05-05 | Bridgestone/Firestone, Inc. | Diene polymers and copolymers terminated by reaction with N-alkyl and N-aryl imines |
| FR2673187B1 (fr) | 1991-02-25 | 1994-07-01 | Michelin & Cie | Composition de caoutchouc et enveloppes de pneumatiques a base de ladite composition. |
| NO300693B1 (no) | 1991-03-06 | 1997-07-07 | Loctite Ireland Ltd | Luftaktiverbare, polymeriserbare blandinger, og anvendelse av disse |
| DE69411984T2 (de) * | 1993-04-30 | 1998-12-10 | Bridgestone Corp., Tokio/Tokyo | Anionische Polymerisationsinitiatoren und Produkte mit niedriger Hysteresis |
| US5310798A (en) * | 1993-08-16 | 1994-05-10 | Bridgestone/Firestone, Inc. | Diene polymers and copolymers terminated with compounds having multiple-bonded nitrogen atoms and partially crosslinked with polyfunctional reagents |
| DE4415658A1 (de) | 1994-05-04 | 1995-11-09 | Bayer Ag | Schwefelhaltige Organosiliciumverbindungen enthaltende Kautschukmischungen |
| DE4417354A1 (de) | 1994-05-18 | 1995-11-23 | Bayer Ag | Kieselsäure-gefüllte Kautschukmischungen mit verbesserter Vulkanisationskinetik |
| DE4435311A1 (de) | 1994-10-01 | 1996-04-04 | Huels Silicone Gmbh | Verstärkungsadditive |
| US5674932A (en) | 1995-03-14 | 1997-10-07 | The Goodyear Tire & Rubber Company | Silica reinforced rubber composition and use in tires |
| US5580919A (en) | 1995-03-14 | 1996-12-03 | The Goodyear Tire & Rubber Company | Silica reinforced rubber composition and use in tires |
| FR2732351B1 (fr) | 1995-03-29 | 1998-08-21 | Michelin & Cie | Composition de caoutchouc pour enveloppe de pneumatique renfermant de la silice dopee aluminium a titre de charge renforcante |
| JPH0987426A (ja) * | 1995-09-20 | 1997-03-31 | Bridgestone Corp | ゴム組成物の製造方法 |
| DE19541404A1 (de) | 1995-11-07 | 1997-05-15 | Degussa | Verfahren zur selektiven Synthese von Silylalkyldisulfiden |
| FR2743564A1 (fr) | 1996-01-11 | 1997-07-18 | Michelin & Cie | Compositions de caoutchouc pour enveloppes de pneumatiques a base de silices contenant un additif de renforcement a base d'un polyorganosiloxane fonctionnalise et d'un compose organosilane . |
| US5675014A (en) | 1996-01-22 | 1997-10-07 | The Goodyear Tire & Rubber Company | Process for the preparation of organosilicon disulfide compounds |
| US5663358A (en) | 1996-01-22 | 1997-09-02 | The Goodyear Tire & Rubber Company | Process for the preparation of organosilicon disulfide compounds |
| US5583245A (en) | 1996-03-06 | 1996-12-10 | The Goodyear Tire & Rubber Company | Preparation of sulfur-containing organosilicon compounds |
| IT1283201B1 (it) | 1996-03-07 | 1998-04-16 | Great Laker Chemical Italia S | Diidropiridine come acceleranti di vulcanizzazione per gomme naturali o sintetiche |
| US5652310A (en) | 1996-03-20 | 1997-07-29 | The Goodyear Tire & Rubber Company | Rubbers having improved interaction with silica |
| FR2749313A1 (fr) | 1996-05-28 | 1997-12-05 | Michelin & Cie | Composition de caoutchouc dienique a base d'alumine en tant que charge renforcante et son utilisation pour la fabrication d'enveloppes de pneumatiques |
| US5696197A (en) | 1996-06-21 | 1997-12-09 | The Goodyear Tire & Rubber Company | Heterogeneous silica carbon black-filled rubber compound |
| US5708053A (en) | 1996-08-15 | 1998-01-13 | The Goodyear Tire & Rubber Company | Silica-filled rubber compositions and the processing thereof |
| US5663396A (en) | 1996-10-31 | 1997-09-02 | The Goodyear Tire & Rubber Company | Preparation of sulfur-containing organosilicon compounds |
| US5684172A (en) | 1997-02-11 | 1997-11-04 | The Goodyear Tire & Rubber Company | Process for the preparation of organosilicon polysulfide compounds |
| US5684171A (en) | 1997-02-11 | 1997-11-04 | The Goodyear Tire & Rubber Company | Process for the preparation of organosilicon polysulfide compounds |
| US5865936A (en) | 1997-03-28 | 1999-02-02 | National Starch And Chemical Investment Holding Corporation | Rapid curing structural acrylic adhesive |
| FR2765881B1 (fr) * | 1997-07-09 | 1999-08-13 | Michelin & Cie | Composition de caoutchouc vulcanisable au soufre contenant de la silice |
| DE19734295C1 (de) | 1997-08-08 | 1999-02-25 | Degussa | Verfahren zur Herstellung von Organosiliciumdisulfanen hoher Reinheit |
| CN1330961C (zh) | 1997-11-28 | 2007-08-08 | 米什兰集团总公司 | 测量颗粒聚集体形式的填料的解聚速率的设备和方法 |
| JP4111590B2 (ja) * | 1998-06-04 | 2008-07-02 | 株式会社ブリヂストン | 重合体の製造方法、得られた重合体、及びそれを用いたゴム組成物 |
| KR20010072010A (ko) | 1998-07-22 | 2001-07-31 | 미첼 롤리에르 | 폴리설파이드 알콕시실란, 엔아민 및 구아니딘 유도체를기본으로 하는 커플링 시스템(백색 충전제/디엔엘라스토머) |
| DE19915281A1 (de) | 1999-04-03 | 2000-10-05 | Degussa | Kautschukmischungen |
-
2000
- 2000-01-24 FR FR0001012A patent/FR2804120A1/fr active Pending
-
2001
- 2001-01-22 WO PCT/EP2001/000662 patent/WO2001055253A1/fr not_active Ceased
- 2001-01-22 DE DE60101001T patent/DE60101001T2/de not_active Expired - Lifetime
- 2001-01-22 AU AU2001230203A patent/AU2001230203A1/en not_active Abandoned
- 2001-01-22 EP EP01902347A patent/EP1268650B1/fr not_active Expired - Lifetime
- 2001-01-22 AT AT01902347T patent/ATE252129T1/de not_active IP Right Cessation
- 2001-01-22 CN CN01804010.1A patent/CN1239592C/zh not_active Expired - Fee Related
- 2001-01-22 JP JP2001561099A patent/JP5033289B2/ja not_active Expired - Fee Related
-
2002
- 2002-07-23 US US10/201,482 patent/US6951897B2/en not_active Expired - Lifetime
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3150401A1 (de) | 2015-09-29 | 2017-04-05 | Continental Reifen Deutschland GmbH | Kautschukmischung und fahrzeugreifen |
| DE102016201195A1 (de) | 2016-01-27 | 2017-07-27 | Continental Reifen Deutschland Gmbh | Kautschukmischung und Fahrzeugreifen |
| DE102016225584A1 (de) | 2016-12-20 | 2018-06-21 | Continental Reifen Deutschland Gmbh | Schwefelvernetzbare Kautschukmischung, Vulkanisat der Kautschukmischung und Fahrzeugreifen |
| DE102016225584B4 (de) | 2016-12-20 | 2023-05-25 | Continental Reifen Deutschland Gmbh | Schwefelvernetzbare Kautschukmischung, Vulkanisat der Kautschukmischung und deren Verwendung in Fahrzeugreifen |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2804120A1 (fr) | 2001-07-27 |
| JP2003530443A (ja) | 2003-10-14 |
| CN1239592C (zh) | 2006-02-01 |
| US6951897B2 (en) | 2005-10-04 |
| CN1395595A (zh) | 2003-02-05 |
| WO2001055253A1 (fr) | 2001-08-02 |
| US20030105242A1 (en) | 2003-06-05 |
| AU2001230203A1 (en) | 2001-08-07 |
| EP1268650A1 (fr) | 2003-01-02 |
| JP5033289B2 (ja) | 2012-09-26 |
| EP1268650B1 (fr) | 2003-10-15 |
| DE60101001D1 (de) | 2003-11-20 |
| ATE252129T1 (de) | 2003-11-15 |
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