TWI519910B - 光阻剝離液組成物及使用它之剝離光阻方法 - Google Patents
光阻剝離液組成物及使用它之剝離光阻方法 Download PDFInfo
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- TWI519910B TWI519910B TW099126775A TW99126775A TWI519910B TW I519910 B TWI519910 B TW I519910B TW 099126775 A TW099126775 A TW 099126775A TW 99126775 A TW99126775 A TW 99126775A TW I519910 B TWI519910 B TW I519910B
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- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- HQFQTTNMBUPQAY-UHFFFAOYSA-N cyclobutylhydrazine Chemical compound NNC1CCC1 HQFQTTNMBUPQAY-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- URQUNWYOBNUYJQ-UHFFFAOYSA-N diazonaphthoquinone Chemical compound C1=CC=C2C(=O)C(=[N]=[N])C=CC2=C1 URQUNWYOBNUYJQ-UHFFFAOYSA-N 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 229940043279 diisopropylamine Drugs 0.000 description 1
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 1
- 239000012972 dimethylethanolamine Substances 0.000 description 1
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002429 hydrazines Chemical class 0.000 description 1
- 150000008624 imidazolidinones Chemical class 0.000 description 1
- 238000005468 ion implantation Methods 0.000 description 1
- 238000010884 ion-beam technique Methods 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- NKQBQVNKUQULLD-UHFFFAOYSA-N n'-methylethanimidamide Chemical compound CNC(C)=N NKQBQVNKUQULLD-UHFFFAOYSA-N 0.000 description 1
- RHSSTVUDNMHOQR-UHFFFAOYSA-N n,n-dimethyl-1-(2-methylpropoxy)methanamine Chemical compound CC(C)COCN(C)C RHSSTVUDNMHOQR-UHFFFAOYSA-N 0.000 description 1
- DAZXVJBJRMWXJP-UHFFFAOYSA-N n,n-dimethylethylamine Chemical compound CCN(C)C DAZXVJBJRMWXJP-UHFFFAOYSA-N 0.000 description 1
- OOHAUGDGCWURIT-UHFFFAOYSA-N n,n-dipentylpentan-1-amine Chemical compound CCCCCN(CCCCC)CCCCC OOHAUGDGCWURIT-UHFFFAOYSA-N 0.000 description 1
- KDCHKULYGWACNY-UHFFFAOYSA-N n-(butoxymethyl)-n-ethylethanamine Chemical compound CCCCOCN(CC)CC KDCHKULYGWACNY-UHFFFAOYSA-N 0.000 description 1
- DDUWYDGMCLTDDC-UHFFFAOYSA-N n-(methoxymethyl)-n-methylethanamine Chemical compound CCN(C)COC DDUWYDGMCLTDDC-UHFFFAOYSA-N 0.000 description 1
- QGRBGPKKFIYPSW-UHFFFAOYSA-N n-ethyl-n-(methoxymethyl)ethanamine Chemical compound CCN(CC)COC QGRBGPKKFIYPSW-UHFFFAOYSA-N 0.000 description 1
- GNVRJGIVDSQCOP-UHFFFAOYSA-N n-ethyl-n-methylethanamine Chemical compound CCN(C)CC GNVRJGIVDSQCOP-UHFFFAOYSA-N 0.000 description 1
- UVBMZKBIZUWTLV-UHFFFAOYSA-N n-methyl-n-propylpropan-1-amine Chemical compound CCCN(C)CCC UVBMZKBIZUWTLV-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 229940100684 pentylamine Drugs 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 1
- 150000004032 porphyrins Chemical class 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 150000004040 pyrrolidinones Chemical class 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical compound CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 description 1
- 238000000527 sonication Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- DQWPFSLDHJDLRL-UHFFFAOYSA-N triethyl phosphate Chemical compound CCOP(=O)(OCC)OCC DQWPFSLDHJDLRL-UHFFFAOYSA-N 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/26—Processing photosensitive materials; Apparatus therefor
- G03F7/42—Stripping or agents therefor
- G03F7/422—Stripping or agents therefor using liquids only
- G03F7/425—Stripping or agents therefor using liquids only containing mineral alkaline compounds; containing organic basic compounds, e.g. quaternary ammonium compounds; containing heterocyclic basic compounds containing nitrogen
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/26—Processing photosensitive materials; Apparatus therefor
- G03F7/42—Stripping or agents therefor
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/027—Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34
- H01L21/0271—Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34 comprising organic layers
- H01L21/0273—Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34 comprising organic layers characterised by the treatment of photoresist layers
- H01L21/0274—Photolithographic processes
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
- C11D2111/10—Objects to be cleaned
- C11D2111/14—Hard surfaces
- C11D2111/22—Electronic devices, e.g. PCBs or semiconductors
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Manufacturing & Machinery (AREA)
- Computer Hardware Design (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Power Engineering (AREA)
- Exposure Of Semiconductors, Excluding Electron Or Ion Beam Exposure (AREA)
- Photosensitive Polymer And Photoresist Processing (AREA)
- Cleaning Or Drying Semiconductors (AREA)
- Cleaning By Liquid Or Steam (AREA)
- Manufacturing Of Printed Circuit Boards (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR20090073762 | 2009-08-11 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW201113652A TW201113652A (en) | 2011-04-16 |
| TWI519910B true TWI519910B (zh) | 2016-02-01 |
Family
ID=43586635
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW099126775A TWI519910B (zh) | 2009-08-11 | 2010-08-11 | 光阻剝離液組成物及使用它之剝離光阻方法 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US9081291B2 (enExample) |
| JP (1) | JP5647685B2 (enExample) |
| KR (1) | KR20110016418A (enExample) |
| CN (1) | CN102472985B (enExample) |
| TW (1) | TWI519910B (enExample) |
| WO (1) | WO2011019189A2 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI861087B (zh) * | 2019-04-09 | 2024-11-11 | 日商東京威力科創股份有限公司 | 減輕圖案崩塌用的使用點清洗溶液混合 |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010090146A1 (ja) * | 2009-02-03 | 2010-08-12 | 出光興産株式会社 | レジスト剥離剤組成物及びそれを用いたレジスト剥離方法 |
| KR100950779B1 (ko) * | 2009-08-25 | 2010-04-02 | 엘티씨 (주) | Tft―lcd 통합공정용 포토레지스트 박리제 조성물 |
| KR101879576B1 (ko) * | 2011-06-29 | 2018-07-18 | 동우 화인켐 주식회사 | 오프셋 인쇄용 요판 세정액 조성물 및 이를 이용한 세정방법 |
| CN103064263B (zh) * | 2011-08-22 | 2015-06-10 | 东友精细化工有限公司 | 抗蚀剂剥离液组合物及利用该组合物的抗蚀剂剥离方法 |
| KR101880302B1 (ko) * | 2011-10-25 | 2018-07-20 | 동우 화인켐 주식회사 | 레지스트 박리액 조성물 및 이를 이용한 레지스트 박리방법 |
| KR101880303B1 (ko) * | 2011-11-04 | 2018-07-20 | 동우 화인켐 주식회사 | 포토레지스트 박리액 조성물 |
| KR20140024625A (ko) * | 2012-08-20 | 2014-03-03 | 주식회사 동진쎄미켐 | 포토레지스트 제거용 박리액 조성물 |
| US20140100151A1 (en) * | 2012-10-08 | 2014-04-10 | Air Products And Chemicals Inc. | Stripping and Cleaning Compositions for Removal of Thick Film Resist |
| CN102956505B (zh) * | 2012-11-19 | 2015-06-17 | 深圳市华星光电技术有限公司 | 开关管的制作方法、阵列基板的制作方法 |
| KR101946379B1 (ko) * | 2012-11-20 | 2019-02-11 | 주식회사 동진쎄미켐 | 포토레지스트 박리액 조성물 및 포토레지스트의 박리방법 |
| US9158202B2 (en) * | 2012-11-21 | 2015-10-13 | Dynaloy, Llc | Process and composition for removing substances from substrates |
| CN103308654B (zh) * | 2013-06-13 | 2016-08-10 | 深圳市华星光电技术有限公司 | 用于测试光阻剥离液中水分含量的方法 |
| KR102119438B1 (ko) * | 2013-10-30 | 2020-06-08 | 삼성디스플레이 주식회사 | 박리액 및 이를 이용한 표시 장치의 제조방법 |
| US9346737B2 (en) * | 2013-12-30 | 2016-05-24 | Eastman Chemical Company | Processes for making cyclohexane compounds |
| KR102092922B1 (ko) * | 2014-03-21 | 2020-04-14 | 동우 화인켐 주식회사 | 레지스트 박리액 조성물 및 이를 이용한 레지스트의 박리방법 |
| KR101586453B1 (ko) * | 2014-08-20 | 2016-01-21 | 주식회사 엘지화학 | 포토레지스트 제거용 스트리퍼 조성물 및 이를 이용한 포토레지스트의 박리방법 |
| US10191380B2 (en) * | 2014-10-14 | 2019-01-29 | Az Electronic Materials (Luxembourg) S.A.R.L. | Composition for resist patterning and method for forming pattern using same |
| KR102347618B1 (ko) * | 2015-04-02 | 2022-01-05 | 동우 화인켐 주식회사 | 레지스트 박리액 조성물 |
| KR102529951B1 (ko) * | 2015-12-14 | 2023-05-08 | 삼성디스플레이 주식회사 | 포토 레지스트 박리제 조성물 및 이를 이용한 박막 트랜지스터 어레이의 제조 방법 |
| KR102422264B1 (ko) * | 2016-03-11 | 2022-07-18 | 주식회사 이엔에프테크놀로지 | 신너 조성물 |
| KR102433114B1 (ko) * | 2016-05-02 | 2022-08-17 | 주식회사 이엔에프테크놀로지 | 신너 조성물 |
| WO2018058341A1 (en) * | 2016-09-28 | 2018-04-05 | Dow Global Technologies Llc | Sulfoxide/glycol ether based solvents for use in the electronics industry |
| KR102465604B1 (ko) * | 2016-11-01 | 2022-11-11 | 주식회사 이엔에프테크놀로지 | 신너 조성물 |
| CN106773562A (zh) * | 2016-12-23 | 2017-05-31 | 昆山艾森半导体材料有限公司 | 一种去除az光刻胶的去胶液 |
| CN108255027B (zh) * | 2016-12-28 | 2024-04-12 | 安集微电子(上海)有限公司 | 一种光刻胶清洗液 |
| JP6899220B2 (ja) * | 2017-01-11 | 2021-07-07 | 株式会社ダイセル | レジスト除去用組成物 |
| KR102434647B1 (ko) | 2017-01-17 | 2022-08-22 | 주식회사 다이셀 | 반도체 기판 세정제 |
| CN108424818A (zh) * | 2017-02-14 | 2018-08-21 | 东友精细化工有限公司 | 掩模清洗液组合物 |
| CN108693717A (zh) * | 2017-03-29 | 2018-10-23 | 东友精细化工有限公司 | 抗蚀剂剥离液组合物 |
| CN108929808B (zh) * | 2017-05-26 | 2020-11-27 | 荒川化学工业株式会社 | 无铅软钎料焊剂用清洗剂组合物、无铅软钎料焊剂的清洗方法 |
| CN107271450A (zh) * | 2017-06-20 | 2017-10-20 | 深圳市华星光电技术有限公司 | 一种聚酰胺/氮化硅膜致密性的检测方法 |
| CN110396315B (zh) * | 2019-07-22 | 2020-11-10 | 深圳市华星光电技术有限公司 | 改性修复液、制备方法及修复色阻的方法 |
| KR102453332B1 (ko) * | 2019-11-20 | 2022-10-11 | 닛산 가가쿠 가부시키가이샤 | 세정제 조성물 및 세정 방법 |
| JP7577906B2 (ja) * | 2020-09-22 | 2024-11-06 | エルジー・ケム・リミテッド | フォトレジスト除去用ストリッパー組成物およびこれを用いたフォトレジストの剥離方法 |
| CN112947015A (zh) * | 2021-02-08 | 2021-06-11 | 绵阳艾萨斯电子材料有限公司 | Pr胶剥离液及其在液晶面板制程再生中的应用 |
| CN116285995A (zh) * | 2021-12-20 | 2023-06-23 | 李长荣化学工业股份有限公司 | 用于移除硅的蚀刻组成物及使用其移除硅的方法 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100528266B1 (ko) * | 1996-03-22 | 2006-03-09 | 바스프 악티엔게젤샤프트 | 건식에칭후측벽잔류물제거용용액및제거방법 |
| DE19801049A1 (de) * | 1998-01-14 | 1999-07-15 | Clariant Gmbh | Verwendung von Formamidinium-Salzen als Bleichaktivatoren |
| KR100761608B1 (ko) * | 2000-07-26 | 2007-09-27 | 미츠비시 가스 가가쿠 가부시키가이샤 | 팔라듐 제거액 및 팔라듐 제거방법 |
| JP2002278092A (ja) * | 2000-12-27 | 2002-09-27 | Sumitomo Chem Co Ltd | 剥離剤組成物 |
| DE60328014D1 (de) * | 2002-04-25 | 2009-07-30 | Fujifilm Electronic Materials | Nicht korrodierende reinigungsmittel zur entfernung von ätzmittelrückständen |
| JP2004029346A (ja) * | 2002-06-25 | 2004-01-29 | Mitsubishi Gas Chem Co Inc | レジスト剥離液組成物 |
| JP4443864B2 (ja) * | 2002-07-12 | 2010-03-31 | 株式会社ルネサステクノロジ | レジストまたはエッチング残さ物除去用洗浄液および半導体装置の製造方法 |
| KR20060024478A (ko) * | 2004-09-13 | 2006-03-17 | 주식회사 동진쎄미켐 | 포토레지스트 박리액 조성물 |
| US20060116313A1 (en) * | 2004-11-30 | 2006-06-01 | Denise Geitz | Compositions comprising tannic acid as corrosion inhibitor |
| KR20060064441A (ko) | 2004-12-08 | 2006-06-13 | 말린크로트 베이커, 인코포레이티드 | 비수성 비부식성 마이크로전자 세정 조성물 |
| US7700533B2 (en) * | 2005-06-23 | 2010-04-20 | Air Products And Chemicals, Inc. | Composition for removal of residue comprising cationic salts and methods using same |
| KR101304723B1 (ko) * | 2006-08-22 | 2013-09-05 | 동우 화인켐 주식회사 | 아미드계 화합물을 포함하는 포토레지스트 박리액 및 이를이용한 박리 방법 |
| JP4617337B2 (ja) * | 2007-06-12 | 2011-01-26 | 富士フイルム株式会社 | パターン形成方法 |
| US8361237B2 (en) * | 2008-12-17 | 2013-01-29 | Air Products And Chemicals, Inc. | Wet clean compositions for CoWP and porous dielectrics |
-
2010
- 2010-08-10 WO PCT/KR2010/005238 patent/WO2011019189A2/ko not_active Ceased
- 2010-08-10 CN CN201080034160.8A patent/CN102472985B/zh active Active
- 2010-08-10 US US13/387,087 patent/US9081291B2/en active Active
- 2010-08-10 JP JP2012524640A patent/JP5647685B2/ja active Active
- 2010-08-10 KR KR1020100076819A patent/KR20110016418A/ko not_active Ceased
- 2010-08-11 TW TW099126775A patent/TWI519910B/zh active
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI861087B (zh) * | 2019-04-09 | 2024-11-11 | 日商東京威力科創股份有限公司 | 減輕圖案崩塌用的使用點清洗溶液混合 |
| US12393121B2 (en) | 2019-04-09 | 2025-08-19 | Tokyo Electron Limited | Point-of-use blending of rinse solutions for EUV processing to mitigate pattern collapse |
Also Published As
| Publication number | Publication date |
|---|---|
| CN102472985B (zh) | 2014-01-08 |
| US20120181248A1 (en) | 2012-07-19 |
| JP5647685B2 (ja) | 2015-01-07 |
| KR20110016418A (ko) | 2011-02-17 |
| WO2011019189A3 (ko) | 2011-06-23 |
| CN102472985A (zh) | 2012-05-23 |
| TW201113652A (en) | 2011-04-16 |
| JP2013501958A (ja) | 2013-01-17 |
| WO2011019189A2 (ko) | 2011-02-17 |
| US9081291B2 (en) | 2015-07-14 |
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