TW201430030A - 包含溶劑之過氧化物-可固化之氟聚合物組合物及其使用方法 - Google Patents
包含溶劑之過氧化物-可固化之氟聚合物組合物及其使用方法 Download PDFInfo
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- TW201430030A TW201430030A TW102140012A TW102140012A TW201430030A TW 201430030 A TW201430030 A TW 201430030A TW 102140012 A TW102140012 A TW 102140012A TW 102140012 A TW102140012 A TW 102140012A TW 201430030 A TW201430030 A TW 201430030A
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- 229940057404 di-(4-tert-butylcyclohexyl)peroxydicarbonate Drugs 0.000 description 1
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- ZPWVASYFFYYZEW-UHFFFAOYSA-L dipotassium hydrogen phosphate Chemical compound [K+].[K+].OP([O-])([O-])=O ZPWVASYFFYYZEW-UHFFFAOYSA-L 0.000 description 1
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- DOUHZFSGSXMPIE-UHFFFAOYSA-N hydroxidooxidosulfur(.) Chemical compound [O]SO DOUHZFSGSXMPIE-UHFFFAOYSA-N 0.000 description 1
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- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- GHXZPUGJZVBLGC-UHFFFAOYSA-N iodoethene Chemical compound IC=C GHXZPUGJZVBLGC-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229910000464 lead oxide Inorganic materials 0.000 description 1
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- 125000005647 linker group Chemical group 0.000 description 1
- 239000011344 liquid material Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- UHNWOJJPXCYKCG-UHFFFAOYSA-L magnesium oxalate Chemical compound [Mg+2].[O-]C(=O)C([O-])=O UHNWOJJPXCYKCG-UHFFFAOYSA-L 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000003947 neutron activation analysis Methods 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 1
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- 102000045222 parkin Human genes 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000010702 perfluoropolyether Substances 0.000 description 1
- 229920005548 perfluoropolymer Polymers 0.000 description 1
- FHHJDRFHHWUPDG-UHFFFAOYSA-L peroxysulfate(2-) Chemical class [O-]OS([O-])(=O)=O FHHJDRFHHWUPDG-UHFFFAOYSA-L 0.000 description 1
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- 230000008569 process Effects 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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- WYKYCHHWIJXDAO-UHFFFAOYSA-N tert-butyl 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOC(C)(C)C WYKYCHHWIJXDAO-UHFFFAOYSA-N 0.000 description 1
- DLSMLZRPNPCXGY-UHFFFAOYSA-N tert-butylperoxy 2-ethylhexyl carbonate Chemical compound CCCCC(CC)COC(=O)OOOC(C)(C)C DLSMLZRPNPCXGY-UHFFFAOYSA-N 0.000 description 1
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
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- 229910021642 ultra pure water Inorganic materials 0.000 description 1
- 239000012498 ultrapure water Substances 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
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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
- C08F214/00—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 a halogen
- C08F214/18—Monomers containing fluorine
- C08F214/28—Hexyfluoropropene
-
- 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
- C08J3/24—Crosslinking, e.g. vulcanising, of macromolecules
-
- 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
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/14—Peroxides
-
- 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
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
- C08K5/34924—Triazines containing cyanurate groups; Tautomers thereof
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D127/00—Coating compositions based on 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 a halogen; Coating compositions based on derivatives of such polymers
- C09D127/02—Coating compositions based on 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 a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
- C09D127/12—Coating compositions based on 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 a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C09D127/16—Homopolymers or copolymers of vinylidene fluoride
-
- 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
- C08J2327/00—Characterised by the use 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 a halogen; Derivatives of such polymers
- C08J2327/02—Characterised by the use 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 a halogen; Derivatives of such polymers not modified by chemical after-treatment
- C08J2327/12—Characterised by the use 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 a halogen; Derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08J2327/16—Homopolymers or copolymers of vinylidene fluoride
-
- 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
- C08J2327/00—Characterised by the use 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 a halogen; Derivatives of such polymers
- C08J2327/02—Characterised by the use 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 a halogen; Derivatives of such polymers not modified by chemical after-treatment
- C08J2327/12—Characterised by the use 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 a halogen; Derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08J2327/20—Homopolymers or copolymers of hexafluoropropene
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Polymerisation Methods In General (AREA)
- Graft Or Block Polymers (AREA)
Applications Claiming Priority (1)
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| US201261722516P | 2012-11-05 | 2012-11-05 |
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| US (2) | US20150299356A1 (OSRAM) |
| EP (1) | EP2914659B1 (OSRAM) |
| JP (2) | JP6371295B2 (OSRAM) |
| KR (1) | KR102120657B1 (OSRAM) |
| CN (1) | CN104870552B (OSRAM) |
| TW (1) | TW201430030A (OSRAM) |
| WO (1) | WO2014071129A1 (OSRAM) |
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| TWI791559B (zh) * | 2017-07-20 | 2023-02-11 | 美商3M新設資產公司 | 藉由光化輻射固化之氟化彈性體及其方法 |
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| EP3469018A1 (en) * | 2016-06-13 | 2019-04-17 | Solvay Specialty Polymers Italy S.p.A. | Curable fluoroelastomer composition |
| US10362698B2 (en) * | 2017-01-20 | 2019-07-23 | Yaskawa America, Inc. | Method and system for environmental sealing of electrical enclosures |
| US12194717B2 (en) * | 2017-11-17 | 2025-01-14 | Daikin Industries, Ltd. | Air management system member and fluororubber composition |
| WO2019126016A1 (en) * | 2017-12-18 | 2019-06-27 | 3M Innovative Properties Company | Fluorinated elastomers cured by actinic radiation and methods thereof |
| JP6784300B2 (ja) * | 2018-02-09 | 2020-11-11 | ダイキン工業株式会社 | フッ素ゴム組成物及びその成形品 |
| US20230026338A1 (en) | 2019-12-30 | 2023-01-26 | 3M Innovative Properties Company | Composition Including Fluoropolymer, Benzoyl Peroxide, and Crosslinker and Related Articles and Methods |
Family Cites Families (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2559752A (en) | 1951-03-06 | 1951-07-10 | Du Pont | Aqueous colloidal dispersions of polymers |
| US3318854A (en) | 1953-04-03 | 1967-05-09 | Minnesota Mining & Mfg | Fluorinated elastomeric copolymers |
| DE1078329B (de) | 1955-04-27 | 1960-03-24 | Du Pont | Verfahren zur Herstellung eines elastischen Mischpolymerisats aus Vinylidenfluorid und einem anderen Fluorolefin |
| US2968649A (en) | 1958-12-04 | 1961-01-17 | Du Pont | Elastomeric terpolymers |
| GB950084A (en) * | 1959-06-24 | 1964-02-19 | Du Pont | Improvements in or relating to fluorine containing copolymers, their production and cured products obtained therefrom |
| US3507844A (en) | 1965-08-03 | 1970-04-21 | Aviat Uk | Fluoroelastomer sealants |
| US3452126A (en) | 1966-12-09 | 1969-06-24 | Us Air Force | Method of post-curing a benzoyl peroxide cured fluoroelastomer composition |
| US4141874A (en) | 1975-11-15 | 1979-02-27 | Daikin Kogyo Co., Ltd. | Fluorine-containing elastomeric copolymers, process for preparing the same and composition containing the same |
| US4621116A (en) | 1984-12-07 | 1986-11-04 | E. I. Du Pont De Nemours And Company | Process for copolymerization of tetrafluoroethylene in the presence of a dispersing agent comprising a perfluoroalkoxybenzene sulfonic acid or salt |
| JPS62263272A (ja) * | 1986-05-09 | 1987-11-16 | Nok Corp | 加硫接着剤配合物 |
| JP3009676B2 (ja) * | 1989-03-31 | 2000-02-14 | 日本バルカー工業株式会社 | フッ素ゴム成形品の製造方法 |
| JP2501044B2 (ja) * | 1991-03-01 | 1996-05-29 | 信越化学工業株式会社 | 液状発泡性フッ素ゴム組成物 |
| JP3160395B2 (ja) | 1992-11-27 | 2001-04-25 | ダイネオン リミティド ライアビリティー カンパニー | フッ素ゴム塗布用組成物 |
| US5285002A (en) | 1993-03-23 | 1994-02-08 | Minnesota Mining And Manufacturing Company | Fluorine-containing polymers and preparation and use thereof |
| US5268405A (en) | 1993-03-31 | 1993-12-07 | E. I. Du Pont De Nemours And Company | Low temperature perfluoroelastomers |
| DE4402694A1 (de) | 1993-06-02 | 1995-08-03 | Hoechst Ag | Verfahren zur Rückgewinnung von fluorierten Carbonsäuren |
| DE19824614A1 (de) | 1998-06-02 | 1999-12-09 | Dyneon Gmbh | Verfahren zur Rückgewinnung von fluorierten Alkansäuren aus Abwässern |
| US6429258B1 (en) | 1999-05-20 | 2002-08-06 | E. I. Du Pont De Nemours & Company | Polymerization of fluoromonomers |
| DE19933696A1 (de) | 1999-07-17 | 2001-01-18 | Dyneon Gmbh | Verfahren zur Rückgewinnung fluorierter Emulgatoren aus wässrigen Phasen |
| US6410630B1 (en) | 1999-12-29 | 2002-06-25 | Pelseal Technologies, Llc | High solids fluoroelastomer compositions |
| US6720360B1 (en) | 2000-02-01 | 2004-04-13 | 3M Innovative Properties Company | Ultra-clean fluoropolymers |
| US6794550B2 (en) | 2000-04-14 | 2004-09-21 | 3M Innovative Properties Company | Method of making an aqueous dispersion of fluoropolymers |
| WO2005003075A1 (ja) | 2003-07-02 | 2005-01-13 | Daikin Industries, Ltd. | フルオロアルキルカルボン酸誘導体、含フッ素重合体の製造方法及び含フッ素重合体水性分散液 |
| WO2005007707A1 (ja) | 2003-07-16 | 2005-01-27 | Daikin Industries, Ltd. | 含フッ素重合体の製造方法、含フッ素重合体水性分散液、2−アシルオキシカルボン酸誘導体及び界面活性剤 |
| EP1681308B1 (en) | 2003-10-22 | 2014-07-09 | Daikin Industries, Ltd. | Method of producing an aqueous tetrafluoroethylene polymer dispersion |
| JP2005220161A (ja) | 2004-02-03 | 2005-08-18 | Three M Innovative Properties Co | 加硫用パーフルオロエラストマー組成物およびパーフルオロエラストマー成型品の製造方法 |
| EP1561729A1 (en) | 2004-02-05 | 2005-08-10 | 3M Innovative Properties Company | Removal of fluorinated surfactants from waste water |
| US20050187331A1 (en) | 2004-02-20 | 2005-08-25 | Yuan Hui L. | Fluoroelastomer gasket compositions |
| JP2006036986A (ja) | 2004-07-28 | 2006-02-09 | Asahi Glass Co Ltd | 含フッ素ポリマーラテックス、その製造方法および含フッ素ポリマー |
| US20060105285A1 (en) * | 2004-11-17 | 2006-05-18 | Naiyong Jing | Nonelastomeric dental article with a protective fluoropolymer layer |
| JP5061446B2 (ja) | 2005-03-04 | 2012-10-31 | 旭硝子株式会社 | 含フッ素エラストマーラテックス、その製造方法、含フッ素エラストマーおよび含フッ素ゴム成形品 |
| GB0525978D0 (en) | 2005-12-21 | 2006-02-01 | 3M Innovative Properties Co | Fluorinated Surfactants For Making Fluoropolymers |
| GB0514387D0 (en) | 2005-07-15 | 2005-08-17 | 3M Innovative Properties Co | Aqueous emulsion polymerization of fluorinated monomers using a perfluoropolyether surfactant |
| US20070015937A1 (en) | 2005-07-15 | 2007-01-18 | 3M Innovative Properties Company | Process for recovery of fluorinated carboxylic acid surfactants from exhaust gas |
| US20070142513A1 (en) | 2005-12-21 | 2007-06-21 | Daikin Industries, Ltd. | Surfactant, method of producing a fluoropolymer, fluoropolymer aqueous dispersion |
| WO2009036131A2 (en) * | 2007-09-14 | 2009-03-19 | 3M Innovative Properties Company | Ultra low viscosity iodine containing amorphous fluoropolymers |
| WO2010147815A2 (en) * | 2009-06-19 | 2010-12-23 | 3M Innovative Properties Company | Low temperature curable amorphous fluoropolymers |
| US20110206878A1 (en) * | 2010-02-25 | 2011-08-25 | Sullivan James P | Reinforced Elastomers |
| JP5607442B2 (ja) * | 2010-07-09 | 2014-10-15 | スリーエム イノベイティブ プロパティズ カンパニー | フルオロポリマー系粘接着性組成物 |
-
2013
- 2013-11-01 US US14/440,693 patent/US20150299356A1/en not_active Abandoned
- 2013-11-01 WO PCT/US2013/067964 patent/WO2014071129A1/en not_active Ceased
- 2013-11-01 EP EP13792154.0A patent/EP2914659B1/en active Active
- 2013-11-01 KR KR1020157014523A patent/KR102120657B1/ko not_active Expired - Fee Related
- 2013-11-01 CN CN201380067497.2A patent/CN104870552B/zh not_active Expired - Fee Related
- 2013-11-01 JP JP2015541814A patent/JP6371295B2/ja active Active
- 2013-11-04 TW TW102140012A patent/TW201430030A/zh unknown
-
2018
- 2018-04-12 JP JP2018076645A patent/JP2018119161A/ja not_active Withdrawn
-
2020
- 2020-02-18 US US16/793,947 patent/US11130829B2/en active Active
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI791559B (zh) * | 2017-07-20 | 2023-02-11 | 美商3M新設資產公司 | 藉由光化輻射固化之氟化彈性體及其方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| JP6371295B2 (ja) | 2018-08-08 |
| JP2018119161A (ja) | 2018-08-02 |
| US20150299356A1 (en) | 2015-10-22 |
| KR20150082430A (ko) | 2015-07-15 |
| WO2014071129A1 (en) | 2014-05-08 |
| EP2914659A1 (en) | 2015-09-09 |
| CN104870552B (zh) | 2018-07-10 |
| KR102120657B1 (ko) | 2020-06-09 |
| US20200181302A1 (en) | 2020-06-11 |
| JP2015533924A (ja) | 2015-11-26 |
| US11130829B2 (en) | 2021-09-28 |
| CN104870552A (zh) | 2015-08-26 |
| EP2914659B1 (en) | 2018-10-03 |
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