JP5965414B2 - 防振ゴム組成物、架橋防振ゴム組成物及び防振ゴム - Google Patents
防振ゴム組成物、架橋防振ゴム組成物及び防振ゴム Download PDFInfo
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- JP5965414B2 JP5965414B2 JP2013556265A JP2013556265A JP5965414B2 JP 5965414 B2 JP5965414 B2 JP 5965414B2 JP 2013556265 A JP2013556265 A JP 2013556265A JP 2013556265 A JP2013556265 A JP 2013556265A JP 5965414 B2 JP5965414 B2 JP 5965414B2
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- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 description 25
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- DBDNZCBRIPTLJF-UHFFFAOYSA-N boron(1-) monohydride Chemical compound [BH-] DBDNZCBRIPTLJF-UHFFFAOYSA-N 0.000 description 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 12
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- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 11
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- 239000003446 ligand Substances 0.000 description 8
- CPOFMOWDMVWCLF-UHFFFAOYSA-N methyl(oxo)alumane Chemical compound C[Al]=O CPOFMOWDMVWCLF-UHFFFAOYSA-N 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 7
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- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 7
- 239000004698 Polyethylene Substances 0.000 description 7
- 125000000217 alkyl group Chemical group 0.000 description 7
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 7
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- 239000007795 chemical reaction product Substances 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 7
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 description 7
- 238000000113 differential scanning calorimetry Methods 0.000 description 7
- UIWYJDYFSGRHKR-UHFFFAOYSA-N gadolinium atom Chemical compound [Gd] UIWYJDYFSGRHKR-UHFFFAOYSA-N 0.000 description 7
- 238000005227 gel permeation chromatography Methods 0.000 description 7
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- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 7
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- 238000002360 preparation method Methods 0.000 description 7
- 150000007944 thiolates Chemical group 0.000 description 7
- GPNYZBKIGXGYNU-UHFFFAOYSA-N 2-tert-butyl-6-[(3-tert-butyl-5-ethyl-2-hydroxyphenyl)methyl]-4-ethylphenol Chemical compound CC(C)(C)C1=CC(CC)=CC(CC=2C(=C(C=C(CC)C=2)C(C)(C)C)O)=C1O GPNYZBKIGXGYNU-UHFFFAOYSA-N 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 6
- 239000007983 Tris buffer Substances 0.000 description 6
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- 150000004703 alkoxides Chemical group 0.000 description 6
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 6
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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 6
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- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
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- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 6
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- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 6
- MCULRUJILOGHCJ-UHFFFAOYSA-N triisobutylaluminium Chemical compound CC(C)C[Al](CC(C)C)CC(C)C MCULRUJILOGHCJ-UHFFFAOYSA-N 0.000 description 6
- YWWDBCBWQNCYNR-UHFFFAOYSA-N trimethylphosphine Chemical compound CP(C)C YWWDBCBWQNCYNR-UHFFFAOYSA-N 0.000 description 6
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 6
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- 230000003712 anti-aging effect Effects 0.000 description 5
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 5
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- 125000002704 decyl group Chemical group [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])* 0.000 description 5
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- XQUPVDVFXZDTLT-UHFFFAOYSA-N 1-[4-[[4-(2,5-dioxopyrrol-1-yl)phenyl]methyl]phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C(C=C1)=CC=C1CC1=CC=C(N2C(C=CC2=O)=O)C=C1 XQUPVDVFXZDTLT-UHFFFAOYSA-N 0.000 description 4
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- NRBXJCXWJPDJFE-UHFFFAOYSA-N C[SiH](C)[NH-].C[SiH](C)[NH-].C=1C=CC=CC=1C1=CC2=CC=CC=C2C1[Gd+2]C(C1=CC=CC=C1C=1)C=1C1=CC=CC=C1 Chemical compound C[SiH](C)[NH-].C[SiH](C)[NH-].C=1C=CC=CC=1C1=CC2=CC=CC=C2C1[Gd+2]C(C1=CC=CC=C1C=1)C=1C1=CC=CC=C1 NRBXJCXWJPDJFE-UHFFFAOYSA-N 0.000 description 4
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- QEFYFXOXNSNQGX-UHFFFAOYSA-N neodymium atom Chemical compound [Nd] QEFYFXOXNSNQGX-UHFFFAOYSA-N 0.000 description 4
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- 150000002894 organic compounds Chemical class 0.000 description 4
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- 125000003638 stannyl group Chemical group [H][Sn]([H])([H])* 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
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- 239000003981 vehicle Substances 0.000 description 4
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Classifications
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- 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
- C08K3/06—Sulfur
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- 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
- C08F297/00—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
- C08F297/06—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type
- C08F297/08—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins
-
- 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
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3415—Five-membered rings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L21/00—Compositions of unspecified rubbers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/16—Ethene-propene or ethene-propene-diene copolymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/18—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms
- C08L23/20—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms having four to nine carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L7/00—Compositions of natural rubber
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Springs (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2012017129 | 2012-01-30 | ||
| JP2012017129 | 2012-01-30 | ||
| PCT/JP2013/000486 WO2013114869A1 (ja) | 2012-01-30 | 2013-01-30 | 防振ゴム組成物、架橋防振ゴム組成物及び防振ゴム |
Publications (2)
| Publication Number | Publication Date |
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| JPWO2013114869A1 JPWO2013114869A1 (ja) | 2015-05-11 |
| JP5965414B2 true JP5965414B2 (ja) | 2016-08-03 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013556265A Expired - Fee Related JP5965414B2 (ja) | 2012-01-30 | 2013-01-30 | 防振ゴム組成物、架橋防振ゴム組成物及び防振ゴム |
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| Country | Link |
|---|---|
| US (1) | US9567448B2 (enExample) |
| EP (1) | EP2810985B1 (enExample) |
| JP (1) | JP5965414B2 (enExample) |
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| BR (1) | BR112014018621A8 (enExample) |
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Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6283572B2 (ja) * | 2014-05-30 | 2018-02-21 | 株式会社ブリヂストン | ゴム組成物及び防振ゴム |
| CN106916383B (zh) * | 2015-12-25 | 2019-06-25 | 比亚迪股份有限公司 | 一种隔音材料组合物和车用隔音片材 |
| EP3998307B1 (en) * | 2019-07-08 | 2024-04-03 | NOK Corporation | Rubber composition for torsional dampers |
| FR3141462A1 (fr) * | 2022-11-02 | 2024-05-03 | Compagnie Generale Des Etablissements Michelin | Copolymères couplés diéniques riches en unités éthylène et leur procédé de préparation |
Family Cites Families (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU504810A1 (ru) * | 1971-11-11 | 1976-02-28 | Предприятие П/Я В-8749 | Резинова смесь |
| JPH0815843B2 (ja) * | 1985-04-16 | 1996-02-21 | 株式会社ブリヂストン | 耐久性の改善された空気入りタイヤ |
| US4808561A (en) | 1985-06-21 | 1989-02-28 | Exxon Chemical Patents Inc. | Supported polymerization catalyst |
| IN172494B (enExample) * | 1986-12-19 | 1993-09-04 | Exxon Chemical Patents Inc | |
| JP2525821B2 (ja) | 1986-11-18 | 1996-08-21 | 株式会社ブリヂストン | タイヤビ−ドフィラ−用ゴム組成物 |
| JPH01118547A (ja) * | 1987-11-02 | 1989-05-11 | Bridgestone Corp | ゴム組成物 |
| JPH062844B2 (ja) | 1988-07-16 | 1994-01-12 | 鬼怒川ゴム工業株式会社 | 防振ゴム組成物 |
| JPH0268937A (ja) * | 1988-09-02 | 1990-03-08 | Nec Yamagata Ltd | ペレットの位置決め装置 |
| JPH0267342A (ja) * | 1988-09-02 | 1990-03-07 | Bridgestone Corp | ゴム組成物 |
| JP2897836B2 (ja) | 1990-03-08 | 1999-05-31 | 株式会社ブリヂストン | 防振ゴム用ゴム組成物 |
| CN101274973A (zh) * | 1997-04-25 | 2008-10-01 | 三井化学株式会社 | α-烯烃/共轭二烯共聚物 |
| SG75157A1 (en) * | 1998-03-06 | 2000-09-19 | Sumitomo Chemical Co | Etylene-isoprene random copolymer |
| CN1120202C (zh) | 1998-07-31 | 2003-09-03 | 山内株式会社 | 具有超低硬度的橡胶防振体 |
| JP2002187987A (ja) * | 2000-12-19 | 2002-07-05 | Jsr Corp | ゴム組成物 |
| CN100523023C (zh) * | 2002-10-16 | 2009-08-05 | 米其林技术公司 | 乙烯/丁二烯共聚物,用于合成其的催化体系和方法 |
| JP4595488B2 (ja) | 2003-12-09 | 2010-12-08 | 東海ゴム工業株式会社 | 防振ゴム組成物 |
| JP5291858B2 (ja) * | 2004-03-16 | 2013-09-18 | 株式会社ブリヂストン | ゴム組成物及びこれを用いた空気入りタイヤ |
| US7166678B2 (en) | 2004-03-31 | 2007-01-23 | The Gates Corporation | Rubber composition and vibration damper using the rubber composition |
| JP2006199792A (ja) | 2005-01-19 | 2006-08-03 | Bridgestone Corp | 防振ゴム用ゴム組成物及び防振ゴム |
| US8800615B2 (en) * | 2005-03-14 | 2014-08-12 | Bridgestone Corporation | Rubber composition and pneumatic tire using the same |
| JP4622618B2 (ja) | 2005-03-28 | 2011-02-02 | 東海ゴム工業株式会社 | 防振ゴム組成物 |
| JP4622619B2 (ja) * | 2005-03-28 | 2011-02-02 | 東海ゴム工業株式会社 | 防振ゴム組成物 |
| US7566748B2 (en) * | 2005-12-19 | 2009-07-28 | The Goodyear Tire & Rubber Company | Pneumatic tire having a rubber component containing N, N′-(m-phenylene) bismaleimide and zinc dibenzyl dithiocarbamate |
| JP2008007546A (ja) | 2006-06-27 | 2008-01-17 | Toyo Tire & Rubber Co Ltd | 防振ゴム組成物及び防振ゴム |
| JP5083870B2 (ja) * | 2007-05-08 | 2012-11-28 | 株式会社ブリヂストン | 共重合体の製造方法 |
| JP5420224B2 (ja) * | 2008-10-20 | 2014-02-19 | 東洋ゴム工業株式会社 | 防振ゴム用ゴム組成物、防振ゴムおよびその製造方法 |
| JP5210801B2 (ja) * | 2008-10-31 | 2013-06-12 | 東洋ゴム工業株式会社 | 防振ゴム用ゴム組成物及び防振ゴム |
| JP2010254872A (ja) * | 2009-04-28 | 2010-11-11 | Bridgestone Corp | 防振ゴム用ゴム組成物 |
| JP2011046795A (ja) | 2009-08-26 | 2011-03-10 | Bridgestone Corp | 防振ゴム組成物及び防振ゴム |
| JP2011148935A (ja) | 2010-01-22 | 2011-08-04 | Bridgestone Corp | タイヤ |
| US8987347B2 (en) | 2011-02-04 | 2015-03-24 | Bridgestone Corporation | Copolymer of conjugated diene compound and non-conjugated olefin, rubber composition, rubber composition for tire tread, crosslinked rubber composition, and tire |
| JP5993879B2 (ja) * | 2012-01-30 | 2016-09-14 | 株式会社ブリヂストン | 防振ゴム組成物、架橋防振ゴム組成物及び防振ゴム |
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- 2013-01-30 BR BR112014018621A patent/BR112014018621A8/pt active Search and Examination
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- 2013-01-30 RU RU2014135381/05A patent/RU2579103C1/ru active
- 2013-01-30 EP EP13743352.0A patent/EP2810985B1/en not_active Not-in-force
- 2013-01-30 JP JP2013556265A patent/JP5965414B2/ja not_active Expired - Fee Related
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Also Published As
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|---|---|
| BR112014018621A8 (pt) | 2017-07-11 |
| WO2013114869A1 (ja) | 2013-08-08 |
| EP2810985B1 (en) | 2017-04-05 |
| EP2810985A1 (en) | 2014-12-10 |
| BR112014018621A2 (enExample) | 2017-06-20 |
| US20150001434A1 (en) | 2015-01-01 |
| CN104204061B (zh) | 2016-08-24 |
| JPWO2013114869A1 (ja) | 2015-05-11 |
| EP2810985A4 (en) | 2015-11-11 |
| CN104204061A (zh) | 2014-12-10 |
| US9567448B2 (en) | 2017-02-14 |
| RU2579103C1 (ru) | 2016-03-27 |
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