KR20170027724A - 폴리아릴렌설파이드 및 그 제조 방법 - Google Patents
폴리아릴렌설파이드 및 그 제조 방법 Download PDFInfo
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- KR20170027724A KR20170027724A KR1020167035870A KR20167035870A KR20170027724A KR 20170027724 A KR20170027724 A KR 20170027724A KR 1020167035870 A KR1020167035870 A KR 1020167035870A KR 20167035870 A KR20167035870 A KR 20167035870A KR 20170027724 A KR20170027724 A KR 20170027724A
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- nitrogen
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- cyclic
- polyarylene sulfide
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- 238000000034 method Methods 0.000 title claims abstract description 99
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- 238000004519 manufacturing process Methods 0.000 title description 40
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- 238000000944 Soxhlet extraction Methods 0.000 description 1
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- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
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- 125000004018 acid anhydride group Chemical group 0.000 description 1
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- 125000003545 alkoxy group Chemical group 0.000 description 1
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- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
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- 230000005540 biological transmission Effects 0.000 description 1
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- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
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- 125000003262 carboxylic acid ester group Chemical group [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
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- 238000005119 centrifugation Methods 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- IBSGAWQJFSDRBJ-UHFFFAOYSA-M cesium sulfanide Chemical compound [SH-].[Cs+] IBSGAWQJFSDRBJ-UHFFFAOYSA-M 0.000 description 1
- 239000012295 chemical reaction liquid Substances 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000011437 continuous method Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 230000006837 decompression Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- QTNDMWXOEPGHBT-UHFFFAOYSA-N dicesium;sulfide Chemical compound [S-2].[Cs+].[Cs+] QTNDMWXOEPGHBT-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
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- 150000002168 ethanoic acid esters Chemical class 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
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- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000002828 fuel tank Substances 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 210000004209 hair Anatomy 0.000 description 1
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- 238000009998 heat setting Methods 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 238000007602 hot air drying Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
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- 235000000396 iron Nutrition 0.000 description 1
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- 238000001840 matrix-assisted laser desorption--ionisation time-of-flight mass spectrometry Methods 0.000 description 1
- 238000002074 melt spinning Methods 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- 150000002829 nitrogen Chemical class 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920006124 polyolefin elastomer Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920001955 polyphenylene ether Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- ZOCLAPYLSUCOGI-UHFFFAOYSA-M potassium hydrosulfide Chemical compound [SH-].[K+] ZOCLAPYLSUCOGI-UHFFFAOYSA-M 0.000 description 1
- DPLVEEXVKBWGHE-UHFFFAOYSA-N potassium sulfide Chemical compound [S-2].[K+].[K+] DPLVEEXVKBWGHE-UHFFFAOYSA-N 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- MWWATHDPGQKSAR-UHFFFAOYSA-N propyne Chemical group CC#C MWWATHDPGQKSAR-UHFFFAOYSA-N 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 1
- LXOXXUIVMOYGST-UHFFFAOYSA-M rubidium(1+);sulfanide Chemical compound [SH-].[Rb+] LXOXXUIVMOYGST-UHFFFAOYSA-M 0.000 description 1
- AHKSSQDILPRNLA-UHFFFAOYSA-N rubidium(1+);sulfide Chemical compound [S-2].[Rb+].[Rb+] AHKSSQDILPRNLA-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000012916 structural analysis Methods 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- 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
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/0204—Polyarylenethioethers
-
- 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
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/0204—Polyarylenethioethers
- C08G75/025—Preparatory processes
- C08G75/0259—Preparatory processes metal hydrogensulfides
-
- 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
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
-
- 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
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/0204—Polyarylenethioethers
- C08G75/0209—Polyarylenethioethers derived from monomers containing one aromatic ring
- C08G75/0213—Polyarylenethioethers derived from monomers containing one aromatic ring containing elements other than carbon, hydrogen or sulfur
-
- 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
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/0204—Polyarylenethioethers
- C08G75/025—Preparatory processes
-
- 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
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/0204—Polyarylenethioethers
- C08G75/0277—Post-polymerisation treatment
- C08G75/0281—Recovery or purification
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2014134152 | 2014-06-30 | ||
| JPJP-P-2014-134152 | 2014-06-30 | ||
| JP2014172348 | 2014-08-27 | ||
| JPJP-P-2014-172348 | 2014-08-27 | ||
| PCT/JP2015/003286 WO2016002210A1 (ja) | 2014-06-30 | 2015-06-30 | ポリアリーレンスルフィドおよびその製造方法 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20170027724A true KR20170027724A (ko) | 2017-03-10 |
Family
ID=55018786
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
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| KR1020167035870A Withdrawn KR20170027724A (ko) | 2014-06-30 | 2015-06-30 | 폴리아릴렌설파이드 및 그 제조 방법 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20170130005A1 (enExample) |
| EP (1) | EP3162839A4 (enExample) |
| JP (2) | JP6123902B2 (enExample) |
| KR (1) | KR20170027724A (enExample) |
| CN (1) | CN106459413A (enExample) |
| WO (1) | WO2016002210A1 (enExample) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102088007B1 (ko) * | 2017-09-20 | 2020-03-11 | 주식회사 엘지화학 | 폴리아릴렌 설파이드의 제조방법 |
| CN109776798B (zh) * | 2018-12-18 | 2020-08-25 | 浙江新和成特种材料有限公司 | 高分子量聚苯硫醚树脂及其制备方法和用途 |
| CN113004520A (zh) * | 2021-04-14 | 2021-06-22 | 深圳市华盈新材料有限公司 | 一种聚苯硫醚树脂的合成工艺 |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05163349A (ja) | 1991-08-06 | 1993-06-29 | Tosoh Corp | ポリアリーレンスルフィドおよびその製造方法 |
| US5869599A (en) | 1995-04-10 | 1999-02-09 | Hay; Allan S. | Free radical ring opening for polymerization of cyclic oligomers containing an aromatic sulfide linkage |
| WO2007034800A1 (ja) | 2005-09-22 | 2007-03-29 | Toray Industries, Inc. | ポリアリーレンスルフィドおよびその製造方法 |
| WO2010074482A2 (ko) | 2008-12-23 | 2010-07-01 | 에스케이케미칼주식회사 | 폴리아릴렌 설파이드의 제조 방법 |
| WO2013147141A1 (ja) | 2012-03-30 | 2013-10-03 | 株式会社クレハ | 粒状ポリアリーレンスルフィド及びその製造方法 |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE69222997T2 (de) * | 1991-08-06 | 1998-04-30 | Tosoh Corp | Verfahren zur Herstellung von Polyarylensulfid |
| JP3141459B2 (ja) * | 1991-10-15 | 2001-03-05 | 東ソー株式会社 | アミノ基含有ポリアリ−レンスルフィドの製造方法 |
| JP4700277B2 (ja) * | 2003-01-21 | 2011-06-15 | 株式会社クレハ | ポリアリーレンスルフィド及びその製造方法 |
| JP4777610B2 (ja) * | 2003-12-26 | 2011-09-21 | 株式会社クレハ | ポリアリーレンスルフィド及びその製造方法 |
| EP1849834B1 (en) * | 2004-12-21 | 2012-08-22 | Polyplastics Co., Ltd. | Polyarylene sulfide resin composition and method for producing same |
| JP2008202164A (ja) * | 2007-02-20 | 2008-09-04 | Toray Ind Inc | ポリフェニレンスルフィド繊維 |
| MY158565A (en) * | 2007-02-28 | 2016-10-14 | Toray Industries | Process for producing cyclic polyarylene sulfide |
| JP2011174033A (ja) * | 2010-01-28 | 2011-09-08 | Toray Ind Inc | 環状ポリアリーレンスルフィドからなる粉体塗料および粉体塗装方法 |
| MY167574A (en) * | 2011-10-24 | 2018-09-20 | Toray Industries | Production method of cyclic polyarylene sulfide |
| US9029484B2 (en) * | 2012-02-29 | 2015-05-12 | Toray Industries, Inc. | Production method of polyarylene sulfide, cyclic polyarylene sulfide pellet and production method thereof |
| EP2843001A4 (en) * | 2012-04-27 | 2016-01-20 | Toray Industries | POLY (ARYLENE SULFIDE) RESIN COMPOSITION, PROCESS FOR PRODUCING THE SAME, AND MOLDED ARTICLE THEREOF |
| JP5888118B2 (ja) * | 2012-05-25 | 2016-03-16 | Dic株式会社 | オリゴアリーレンスルフィドおよびカルボキシアルキルアミノ基含有化合物の製造方法 |
| JP6136292B2 (ja) * | 2013-01-25 | 2017-05-31 | Dic株式会社 | ポリアリーレンスルフィドの製造方法 |
-
2015
- 2015-06-30 WO PCT/JP2015/003286 patent/WO2016002210A1/ja not_active Ceased
- 2015-06-30 US US15/321,952 patent/US20170130005A1/en not_active Abandoned
- 2015-06-30 CN CN201580034390.7A patent/CN106459413A/zh active Pending
- 2015-06-30 KR KR1020167035870A patent/KR20170027724A/ko not_active Withdrawn
- 2015-06-30 EP EP15815458.3A patent/EP3162839A4/en not_active Withdrawn
- 2015-06-30 JP JP2015535906A patent/JP6123902B2/ja active Active
-
2017
- 2017-02-03 JP JP2017018335A patent/JP2017075337A/ja active Pending
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05163349A (ja) | 1991-08-06 | 1993-06-29 | Tosoh Corp | ポリアリーレンスルフィドおよびその製造方法 |
| US5869599A (en) | 1995-04-10 | 1999-02-09 | Hay; Allan S. | Free radical ring opening for polymerization of cyclic oligomers containing an aromatic sulfide linkage |
| WO2007034800A1 (ja) | 2005-09-22 | 2007-03-29 | Toray Industries, Inc. | ポリアリーレンスルフィドおよびその製造方法 |
| WO2010074482A2 (ko) | 2008-12-23 | 2010-07-01 | 에스케이케미칼주식회사 | 폴리아릴렌 설파이드의 제조 방법 |
| WO2013147141A1 (ja) | 2012-03-30 | 2013-10-03 | 株式会社クレハ | 粒状ポリアリーレンスルフィド及びその製造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP3162839A1 (en) | 2017-05-03 |
| CN106459413A (zh) | 2017-02-22 |
| JPWO2016002210A1 (ja) | 2017-04-27 |
| JP6123902B2 (ja) | 2017-05-10 |
| JP2017075337A (ja) | 2017-04-20 |
| EP3162839A4 (en) | 2018-01-10 |
| WO2016002210A1 (ja) | 2016-01-07 |
| US20170130005A1 (en) | 2017-05-11 |
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