JP5179387B2 - キンク化剛直棒状ポリアリーレンの新規な使用、および前記キンク化剛直棒状ポリアリーレンから製造される物品 - Google Patents
キンク化剛直棒状ポリアリーレンの新規な使用、および前記キンク化剛直棒状ポリアリーレンから製造される物品 Download PDFInfo
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- JP5179387B2 JP5179387B2 JP2008557743A JP2008557743A JP5179387B2 JP 5179387 B2 JP5179387 B2 JP 5179387B2 JP 2008557743 A JP2008557743 A JP 2008557743A JP 2008557743 A JP2008557743 A JP 2008557743A JP 5179387 B2 JP5179387 B2 JP 5179387B2
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- Prior art keywords
- polyarylene
- rigid rod
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- phenylene
- kinked
- Prior art date
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- WIPXWWURGIFNRP-UHFFFAOYSA-N (1-chlorocyclohexa-2,4-dien-1-yl)-(4-chlorophenyl)methanone;(2,5-dichlorophenyl)-phenylmethanone Chemical compound C1=CC(Cl)=CC=C1C(=O)C1(Cl)C=CC=CC1.ClC1=CC=C(Cl)C(C(=O)C=2C=CC=CC=2)=C1 WIPXWWURGIFNRP-UHFFFAOYSA-N 0.000 description 1
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Classifications
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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
- C08L65/00—Compositions of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Compositions of derivatives of such polymers
-
- 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
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/04—Reinforcing macromolecular compounds with loose or coherent fibrous material
- C08J5/0405—Reinforcing macromolecular compounds with loose or coherent fibrous material with inorganic fibres
- C08J5/043—Reinforcing macromolecular compounds with loose or coherent fibrous material with inorganic fibres with glass fibres
-
- 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
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L65/00—Compositions of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Compositions of derivatives of such polymers
- C08L65/02—Polyphenylenes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
- C08G2261/31—Monomer units or repeat units incorporating structural elements in the main chain incorporating aromatic structural elements in the main chain
- C08G2261/312—Non-condensed aromatic systems, e.g. benzene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2650/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G2650/28—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type
- C08G2650/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type containing oxygen in addition to the ether group
- C08G2650/40—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type containing oxygen in addition to the ether group containing ketone groups, e.g. polyarylethylketones, PEEK or PEK
-
- 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
- C08J2365/00—Characterised by the use of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Derivatives of such polymers
- C08J2365/02—Polyphenylenes
-
- 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
- C08J2371/00—Characterised by the use of polyethers obtained by reactions forming an ether link in the main chain; Derivatives of such polymers
- C08J2371/08—Polyethers derived from hydroxy compounds or from their metallic derivatives
- C08J2371/10—Polyethers derived from hydroxy compounds or from their metallic derivatives from phenols
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
-
- 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
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
-
- 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
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31678—Of metal
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
- Laminated Bodies (AREA)
Applications Claiming Priority (15)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EPPCT/EP2006/060535 | 2006-03-07 | ||
| PCT/EP2006/060535 WO2006094988A2 (en) | 2005-03-07 | 2006-03-07 | Polyphenylene-poly(aryl ether sulfone) blends, articles and method |
| US83694606P | 2006-08-11 | 2006-08-11 | |
| US60/836,946 | 2006-08-11 | ||
| US84236806P | 2006-09-06 | 2006-09-06 | |
| US84236606P | 2006-09-06 | 2006-09-06 | |
| US84236506P | 2006-09-06 | 2006-09-06 | |
| US84236706P | 2006-09-06 | 2006-09-06 | |
| US84236906P | 2006-09-06 | 2006-09-06 | |
| US60/842,365 | 2006-09-06 | ||
| US60/842,368 | 2006-09-06 | ||
| US60/842,366 | 2006-09-06 | ||
| US60/842,367 | 2006-09-06 | ||
| US60/842,369 | 2006-09-06 | ||
| PCT/EP2007/052073 WO2007101845A2 (en) | 2006-03-07 | 2007-03-06 | New use of a kinked rigid-rod polyarylene, and articles made from said kinked rigid-rod polyarylene |
Publications (3)
| Publication Number | Publication Date |
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| JP2009529077A JP2009529077A (ja) | 2009-08-13 |
| JP2009529077A5 JP2009529077A5 (enExample) | 2010-04-22 |
| JP5179387B2 true JP5179387B2 (ja) | 2013-04-10 |
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| JP2008557751A Active JP5252400B2 (ja) | 2006-03-07 | 2007-03-06 | 新規なポリアリーレン組成物 |
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| JP2008557751A Active JP5252400B2 (ja) | 2006-03-07 | 2007-03-06 | 新規なポリアリーレン組成物 |
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| US (3) | US7875696B2 (enExample) |
| EP (2) | EP1994093B1 (enExample) |
| JP (2) | JP5179387B2 (enExample) |
| AT (2) | ATE517946T1 (enExample) |
| IN (1) | IN2008CH04665A (enExample) |
| WO (3) | WO2007101847A2 (enExample) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7875696B2 (en) | 2006-03-07 | 2011-01-25 | Solvay Advanced Polymers, L.L.C. | Use of a kinked rigid-rod polyarylene, and articles made from said kinked rigid-rod polyarylene |
| US20080312387A1 (en) | 2006-08-11 | 2008-12-18 | Solvay Advanced Polymers, L.L.C. | New Polyarylene Composition |
| US7820767B2 (en) | 2006-03-07 | 2010-10-26 | Solvay Advanced Polymers, L.L.C. | Aromatic polyimide composition |
| EP2064286B1 (en) * | 2006-09-06 | 2010-12-15 | Solvay Advanced Polymers, L.L.C. | New aromatic polycarbonate composition |
| WO2009034087A2 (en) * | 2007-09-11 | 2009-03-19 | Solvay Advanced Polymers, L.L.C. | New prosthetic devices |
| US8119764B2 (en) | 2007-09-11 | 2012-02-21 | Solvay Advanced Polymers, L.L.C. | Medical devices made of a polymer material |
| US8742064B2 (en) * | 2007-10-23 | 2014-06-03 | Solvay Advanced Polymers, L.L.C. | Medical tubings made of a polymer material |
| EP2393857B1 (en) | 2009-02-05 | 2019-05-29 | Arkema Inc. | Assemblies containing polyetherketoneketone tie layers |
| WO2010112436A1 (en) * | 2009-03-30 | 2010-10-07 | Solvay Advanced Polymers, L.L.C. | Threaded fasteners made of a polymer material |
| JP5702283B2 (ja) * | 2009-07-09 | 2015-04-15 | ダイセル・エボニック株式会社 | 熱可塑性樹脂組成物及びその成形体 |
| US9120898B2 (en) | 2011-07-08 | 2015-09-01 | Baker Hughes Incorporated | Method of curing thermoplastic polymer for shape memory material |
| US8939222B2 (en) | 2011-09-12 | 2015-01-27 | Baker Hughes Incorporated | Shaped memory polyphenylene sulfide (PPS) for downhole packer applications |
| US8829119B2 (en) * | 2011-09-27 | 2014-09-09 | Baker Hughes Incorporated | Polyarylene compositions for downhole applications, methods of manufacture, and uses thereof |
| US9144925B2 (en) | 2012-01-04 | 2015-09-29 | Baker Hughes Incorporated | Shape memory polyphenylene sulfide manufacturing, process, and composition |
| WO2014086744A1 (en) * | 2012-12-06 | 2014-06-12 | Solvay Specialty Polymers Usa, Llc | Polyarylene foam materials |
| US9707642B2 (en) | 2012-12-07 | 2017-07-18 | Baker Hughes Incorporated | Toughened solder for downhole applications, methods of manufacture thereof and articles comprising the same |
| WO2014130275A2 (en) | 2013-02-22 | 2014-08-28 | Ticona Llc | High performance polymer composition with improved flow properties |
| CN106574184A (zh) | 2014-08-21 | 2017-04-19 | 提克纳有限责任公司 | 包含聚芳基醚酮和低环烷液晶聚合物的组合物 |
| EP3183321A1 (en) | 2014-08-21 | 2017-06-28 | Ticona LLC | Polyaryletherketone composition |
| US20170349699A1 (en) * | 2014-12-22 | 2017-12-07 | Solvay Specialty Polymers Usa, Llc | Polyphenylene fibers and corresponding fabrication methods |
| DE102015204494B4 (de) * | 2015-03-12 | 2025-06-18 | Hyundai Motor Company | Hybrid-Seitenschweller für ein Kraftfahrzeug und Herstellungsverfahren desselben |
| US11352480B2 (en) * | 2016-03-18 | 2022-06-07 | Ticona Llc | Polyaryletherketone composition |
| WO2019129595A1 (en) * | 2017-12-27 | 2019-07-04 | Solvay Specialty Polymers Usa, Llc | Method for manufacturing a three-dimensional object |
| US11118053B2 (en) | 2018-03-09 | 2021-09-14 | Ticona Llc | Polyaryletherketone/polyarylene sulfide composition |
| CN112513557B (zh) * | 2018-07-30 | 2023-11-21 | 高新特殊工程塑料全球技术有限公司 | 包含聚合物药筒壳的轻量弹药制品 |
| KR102754519B1 (ko) * | 2019-10-31 | 2025-01-14 | 한화솔루션 주식회사 | 결정화 속도가 향상된 고분자 조성물 및 그의 제조방법 |
| KR20230148412A (ko) * | 2021-02-22 | 2023-10-24 | 솔베이 스페셜티 폴리머즈 유에스에이, 엘.엘.씨. | 고 경도 필름 |
Family Cites Families (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA847963A (en) | 1970-07-28 | Zutty Nathan | Process for preparing polyarylene polyethers | |
| GB1586972A (en) * | 1977-02-01 | 1981-03-25 | Ici Ltd | Production of aromatic polyethers |
| US4365037A (en) * | 1980-07-18 | 1982-12-21 | Dainippon Ink & Chemicals, Inc. | Glass fiber-reinforced polyarylene sulfide resin composition |
| JPS6137417A (ja) * | 1984-07-31 | 1986-02-22 | Sumitomo Bakelite Co Ltd | 熱可塑性ポリエーテルエーテルケトンフイルムの製造方法 |
| US5646231A (en) * | 1988-02-17 | 1997-07-08 | Maxdem, Incorporated | Rigid-rod polymers |
| US5227457A (en) * | 1988-02-17 | 1993-07-13 | Maxdem Incorporated | Rigid-rod polymers |
| US5565543A (en) * | 1988-02-17 | 1996-10-15 | Maxdem Incorporated | Rigid-rod polymers |
| US5654392A (en) | 1988-02-17 | 1997-08-05 | Maxdem Incorporated | Rigid-rod polymers |
| DE3931649A1 (de) * | 1989-09-22 | 1991-04-04 | Basf Ag | Thermoplastische formmassen aus faserverstaerkten hochtemperaturbestaendigen thermoplasten |
| DE4001915A1 (de) | 1989-12-06 | 1991-06-13 | Bayer Ag | Mischungen aus substituierten homo-poly-p-phenylenen und thermoplasten |
| DE4015542A1 (de) | 1990-05-15 | 1991-11-21 | Bayer Ag | Mischungen aus substituierten co-poly-p-phenylenen und polycarbonaten und/oder polyestercarbonaten |
| EP0599886B1 (en) * | 1991-08-19 | 2001-03-21 | Mississippi Polymer Technologies, Inc. | Macromonomers having reactive end groups |
| US5869592A (en) * | 1991-08-19 | 1999-02-09 | Maxdem Incorporated | Macromonomers having reactive side groups |
| CA2130004C (en) | 1992-03-06 | 2007-04-24 | Matthew L. Marrocco, Iii | Rigid-rod polymers |
| JPH07506861A (ja) * | 1992-05-15 | 1995-07-27 | セラニーズ・アセテート・リミテッド・ライアビリティ・カンパニー | 強化された射出成形可能なブレンド |
| DE19535086B4 (de) * | 1995-09-21 | 2004-08-12 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Verwendung von polymeren Festkörperelektrolyten sowie Verfahren zu deren Herstellung |
| US5886130A (en) * | 1995-11-02 | 1999-03-23 | Maxdem Incorporated | Polyphenylene co-polymers |
| US5668245A (en) * | 1995-11-02 | 1997-09-16 | Maxdem Incorporated | Polymers with heterocyclic side groups |
| JP4104680B2 (ja) * | 1995-11-09 | 2008-06-18 | ミシシッピ ポリマー テクノロジーズ | 複素環式側基を有するポリマー |
| JP4104679B2 (ja) * | 1995-11-09 | 2008-06-18 | ミシシッピ ポリマー テクノロジーズ | ポリフェニレンコポリマー |
| DE69528463T2 (de) | 1995-11-09 | 2003-02-06 | Mississippi Polymer Technologies, Inc. | Polyphenylencopolymere |
| JP4031595B2 (ja) | 1999-07-15 | 2008-01-09 | 独立行政法人科学技術振興機構 | ポリアリーレン及びその製造方法 |
| JP2001115087A (ja) | 1999-10-20 | 2001-04-24 | Nissan Chem Ind Ltd | 高屈折率ハードコート膜及び反射防止基材 |
| JP2001116904A (ja) | 1999-10-20 | 2001-04-27 | Nissan Chem Ind Ltd | 多層反射防止膜 |
| JP3733516B2 (ja) * | 1999-12-27 | 2006-01-11 | 独立行政法人科学技術振興機構 | 高分子化合物 |
| GB2355464B (en) * | 2000-02-11 | 2004-08-11 | Victrex Mfg Ltd | Aromatic polyetherketones |
| GB2364319B (en) * | 2000-07-06 | 2003-01-15 | Gharda Chemicals Ltd | Melt processible polyether ether ketone polymer |
| JP2003073461A (ja) | 2001-08-31 | 2003-03-12 | Sony Corp | 真空表示管用強化フィルムとこれを用いた真空表示管 |
| JP4583705B2 (ja) * | 2002-11-28 | 2010-11-17 | トヨタ自動車株式会社 | 含燐高分子化合物、その合成方法、高耐久性固体高分子電解質組成物、及び燃料電池 |
| JP2007526393A (ja) | 2004-03-04 | 2007-09-13 | ソルヴェイ アドバンスド ポリマーズ リミテッド ライアビリティ カンパニー | 枝分かれしたポリフェニレンポリマー |
| US8240252B2 (en) | 2005-03-07 | 2012-08-14 | Nikica Maljkovic | Ammunition casing |
| JP5020535B2 (ja) * | 2005-05-09 | 2012-09-05 | 住友化学株式会社 | 芳香族重合体およびその製造方法 |
| JP5004149B2 (ja) * | 2006-02-10 | 2012-08-22 | 住友化学株式会社 | 新規な芳香族重合体 |
| US20080312387A1 (en) * | 2006-08-11 | 2008-12-18 | Solvay Advanced Polymers, L.L.C. | New Polyarylene Composition |
| US7875696B2 (en) | 2006-03-07 | 2011-01-25 | Solvay Advanced Polymers, L.L.C. | Use of a kinked rigid-rod polyarylene, and articles made from said kinked rigid-rod polyarylene |
| US7820767B2 (en) * | 2006-03-07 | 2010-10-26 | Solvay Advanced Polymers, L.L.C. | Aromatic polyimide composition |
| EP1994094B1 (en) | 2006-03-07 | 2010-11-10 | Solvay Advanced Polymers, L.L.C. | New aromatic polyimide composition |
| EP2064286B1 (en) | 2006-09-06 | 2010-12-15 | Solvay Advanced Polymers, L.L.C. | New aromatic polycarbonate composition |
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- 2007-03-06 EP EP20070726660 patent/EP1994093B1/en active Active
- 2007-03-06 JP JP2008557743A patent/JP5179387B2/ja not_active Expired - Fee Related
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| EP1994093A2 (en) | 2008-11-26 |
| US20110046292A1 (en) | 2011-02-24 |
| JP2009529079A (ja) | 2009-08-13 |
| US20090036594A1 (en) | 2009-02-05 |
| US7875696B2 (en) | 2011-01-25 |
| ATE517946T1 (de) | 2011-08-15 |
| EP1994092A2 (en) | 2008-11-26 |
| WO2007101857A3 (en) | 2008-01-03 |
| US8048966B2 (en) | 2011-11-01 |
| US8754162B2 (en) | 2014-06-17 |
| JP5252400B2 (ja) | 2013-07-31 |
| JP2009529077A (ja) | 2009-08-13 |
| WO2007101847A2 (en) | 2007-09-13 |
| WO2007101857A2 (en) | 2007-09-13 |
| EP1994093B1 (en) | 2011-07-27 |
| EP1994092B1 (en) | 2011-10-05 |
| WO2007101845A3 (en) | 2008-02-28 |
| IN2008CH04665A (enExample) | 2009-03-13 |
| ATE527314T1 (de) | 2011-10-15 |
| WO2007101845A2 (en) | 2007-09-13 |
| WO2007101847A3 (en) | 2007-12-27 |
| US20090234077A1 (en) | 2009-09-17 |
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