JP2010163566A - エポキシ樹脂組成物 - Google Patents
エポキシ樹脂組成物 Download PDFInfo
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- JP2010163566A JP2010163566A JP2009008198A JP2009008198A JP2010163566A JP 2010163566 A JP2010163566 A JP 2010163566A JP 2009008198 A JP2009008198 A JP 2009008198A JP 2009008198 A JP2009008198 A JP 2009008198A JP 2010163566 A JP2010163566 A JP 2010163566A
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- epoxy
- epoxy resin
- resin composition
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- 239000003822 epoxy resin Substances 0.000 title claims abstract description 51
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- 239000004305 biphenyl Substances 0.000 claims description 22
- 235000010290 biphenyl Nutrition 0.000 claims description 22
- 239000003054 catalyst Substances 0.000 claims description 14
- -1 oxetane compound Chemical class 0.000 claims description 9
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- 125000002091 cationic group Chemical group 0.000 claims description 6
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- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
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- FNYWFRSQRHGKJT-UHFFFAOYSA-N 3-ethyl-3-[(3-ethyloxetan-3-yl)methoxymethyl]oxetane Chemical compound C1OCC1(CC)COCC1(CC)COC1 FNYWFRSQRHGKJT-UHFFFAOYSA-N 0.000 description 1
- URDOJQUSEUXVRP-UHFFFAOYSA-N 3-triethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CCO[Si](OCC)(OCC)CCCOC(=O)C(C)=C URDOJQUSEUXVRP-UHFFFAOYSA-N 0.000 description 1
- UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 1
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 1
- KBQVDAIIQCXKPI-UHFFFAOYSA-N 3-trimethoxysilylpropyl prop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C=C KBQVDAIIQCXKPI-UHFFFAOYSA-N 0.000 description 1
- PRKPGWQEKNEVEU-UHFFFAOYSA-N 4-methyl-n-(3-triethoxysilylpropyl)pentan-2-imine Chemical compound CCO[Si](OCC)(OCC)CCCN=C(C)CC(C)C PRKPGWQEKNEVEU-UHFFFAOYSA-N 0.000 description 1
- 229910002012 Aerosil® Inorganic materials 0.000 description 1
- 229910052582 BN Inorganic materials 0.000 description 1
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- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- HTELVDHNLPTJDW-UHFFFAOYSA-N C=1C=C(C=2C(=CC(OCC3(CC)COC3)=CC=2)C)C=CC=1OCC1(CC)COC1 Chemical group C=1C=C(C=2C(=CC(OCC3(CC)COC3)=CC=2)C)C=CC=1OCC1(CC)COC1 HTELVDHNLPTJDW-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 description 1
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- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical class C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
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- FRGPKMWIYVTFIQ-UHFFFAOYSA-N triethoxy(3-isocyanatopropyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCN=C=O FRGPKMWIYVTFIQ-UHFFFAOYSA-N 0.000 description 1
- VTHOKNTVYKTUPI-UHFFFAOYSA-N triethoxy-[3-(3-triethoxysilylpropyltetrasulfanyl)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCSSSSCCC[Si](OCC)(OCC)OCC VTHOKNTVYKTUPI-UHFFFAOYSA-N 0.000 description 1
- DQZNLOXENNXVAD-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OC)(OC)OC)CCC2OC21 DQZNLOXENNXVAD-UHFFFAOYSA-N 0.000 description 1
- 125000006839 xylylene group Chemical group 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/02—Details
- H05B33/04—Sealing arrangements, e.g. against humidity
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
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- C—CHEMISTRY; METALLURGY
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Abstract
【解決手段】(a)エポキシ化合物、及び、
(b)前記エポキシ化合物と反応性の架橋性基を2個以上有する化合物、
を含むエポキシ樹脂組成物であって、
(a)/(b)の質量比が0.3〜3であり、そして前記エポキシ樹脂組成物の屈折率が1.6以上である、
エポキシ樹脂組成物。
【選択図】なし
Description
1.
(a)エポキシ化合物、及び、
(b)前記エポキシ化合物と反応性の架橋性基を2個以上有する化合物、
を含むエポキシ樹脂組成物であって、
(a)/(b)の質量比が0.3〜3であり、そして前記エポキシ樹脂組成物の屈折率が1.6以上である、
エポキシ樹脂組成物。
前記エポキシ化合物はビフェニル構造を有する、上記(1)記載のエポキシ樹脂組成物。
前記エポキシ化合物と反応性の架橋性基を2個以上有する化合物(b)は、多価エポキシ化合物、多価オキセタン化合物及びポリオールからなる群より選ばれる、上記(1)又は(2)記載のエポキシ樹脂組成物。
(a)ビフェニル構造を有するエポキシ化合物、及び、
(b)前記エポキシ化合物と反応性の架橋性基を2個以上有する化合物、
を含むエポキシ樹脂組成物であって、
(a)/(b)の質量比が0.3〜3である、エポキシ樹脂組成物。
ビフェニル構造を有するエポキシ化合物は単官能エポキシ化合物である、上記(4)記載のエポキシ樹脂組成物。
カチオン硬化触媒をさらに含む、上記(4)又は(5)記載のエポキシ樹脂組成物。
前記エポキシ化合物と反応性の架橋性基を2個以上有する化合物(b)は、多価エポキシ化合物、多価オキセタン化合物及びポリオールからなる群より選ばれる、上記(4)〜(6)のいずれか1項記載のエポキシ樹脂組成物。
上記(1)〜(7)のいずれか1項記載の(a)及び(b)から形成されるエポキシ樹脂組成物を用いた電子機器。
上述のとおり、本発明のエポキシ樹脂組成物は、(a)エポキシ化合物、及び、
(b)前記エポキシ化合物と反応性の架橋性基を2個以上有する化合物、
を含むエポキシ樹脂組成物であって、
(a)/(b)の質量比が0.3〜3である。エポキシ樹脂組成物の屈折率は、たとえば、1.6以上である。
フィラーの粒子径は特に限定されないが、組成物を透明性が必要な用途に用いる場合には、1nmから100nmのフィラーを用いた場合に、組成物の透明性が損なわれにくいので特に好ましい。
フィラーの屈折率は特に限定されず、1.3〜2.8のものが使用できるが、組成物の透明性が必要な用途で用いられる場合、1.5〜2.4が、屈折率向上させるためには1.6〜2.8のものが好ましい。
これらのフィラーは、エポキシ樹脂への分散性を向上させるたり、吸水率を低下させるために表面処理されていてもよい。
なお、粒子径の測定は、一般に粒子サイズに応じて測定方法が選択されるが、たとえば、広い範囲平均粒子径をカバーする電子顕微鏡による画像解析法、平均粒子径が100nm以下の場合の動的光散乱法(JISZ8826:2005年制定)、平均粒子径が100nm以上の場合のレーザー回折散乱法(JISZ8825:2001年制定)で測定した値を用いることができる。
実施例1
封止剤組成物の調製
ビフェニル構造を有する単官能エポキシ化合物(OPP−G 三光社製)50重量部、ビスフェノールA型エポキシ樹脂(東都化成社製、YD8125)50重量部、カチオン系光硬化触媒(CPI-210S、サンアプロ製)0.5重量部、増感剤(東京化成製 4−ヒドロキシベンゾフェノン)0.1重量部を混合し、粘度3300mPasの組成物を得た。
測定用のサンプルは以下のとおりに調製した。まず、上記のとおりに調製した組成物を、厚み38μmの剥離処理したポリエチレンテレフタレート(PET)フィルム上にコーティングし、その上に、同一の剥離処理したポリエチレンテレフタレート(PET)フィルムに配置した。紫外線(Fusion株式会社製 F300S(Hバルブ使用)、100mJを20回)を照射し、80℃のオーブンで60分間硬化した。これにより、100μmの厚さの透明なフィルムが得られた。
可視光透過率の測定は、分光器U−4000を用いて行った。測定用のサンプルは上記の方法で作成した厚み100μmのフィルムを用いた。波長域400nm〜800nmの範囲での平均の透過率を表2に示す。
屈折率の測定はアタゴ社製アッベ屈折率計を用い、室温(23℃)においてNa−D線における屈折率を測定した。測定用のサンプルは、上記の方法で作成した厚み100μmのフィルムを10mm×20mmにカットしたものを用いた。サンプルと屈折率計のプリズム面との間には中間液としてαブロムナフタリン(屈折率nD=1.657)を用いた。
材料を表1に記載のとおりに変更した以外は、実施例1と同様に組成物を調製し、同様に評価を行った。
表1に示すとおりの材料をメチルエチルケトン(MEK)中に溶解させ、30重量%の溶液とした後に、ナイフコータを用いて厚み38μmの剥離処理したPETフィルムにコーティングし、厚み100μmの透明なフィルムを得た。以後は、実施例1と同様に評価した。
樹脂2(エポキシ基と反応性の架橋性基を2個以上有する化合物):ビスフェノールAジグリシジルエーテル(YD8125、東都化成社製)
樹脂3:ジ(グリシジルメチルトリシクロデカン)(アデカ株式会社製、EP4088S)
樹脂4:4,4’−ビス[(3−エチルオキセタン−3−イル)メトキシ]メチルビフェニル(OXBP,宇部興産株式会社製)
樹脂5:ビスフェノールフルオレンジグリシジルエーテル(EX1010,大阪ガス化学株式会社製)
樹脂6:フェノキシ樹脂(YP50、東都化成社製)
硬化触媒1:芳香族スルホニウムパーフルオロアルキルフロロホスフェート(カチオン硬化触媒系・CPI-210S、サンアプロ製)
硬化触媒2:芳香族ヨードニウムパーフルオロフェニルボレート(カチオン硬化触媒系・2074、ローディア製)
染料増感剤1:(4−ヒドロキシベンゾフェノン、東京化成製)
染料増感剤2:2,9−ブトキシアントラキノン(UVS−1331,川崎化学工業株式会社製)
カップリング剤1:3−グリシドキシプロピルトリメトキシシラン(KBM403 信越化学株式会社製)
フィラー1:ヒュームドシリカ(R972、平均粒子径16nm、日本アエロジル株式会社製)(平均粒子径の測定は上記の通りの電子顕微鏡による画像解析法によって行なったものである。)
フィラー2:ヒュームドシリカ(FB−3SDC,平均粒子径3.4μm、電気化学工業株式会社製)(平均粒子径の測定は上記の通りのレーザー回折散乱法によって行なったものである。)
20 紫外線発光ダイオード(LED)素子
1 基板
2 回路
3 発光機能を司る積層体
4 パッシベーション膜
5 封止剤
6 保護層
Claims (8)
- (a)エポキシ化合物、及び、
(b)前記エポキシ化合物と反応性の架橋性基を2個以上有する化合物、
を含むエポキシ樹脂組成物であって、
(a)/(b)の質量比が0.3〜3であり、そして前記エポキシ樹脂組成物の屈折率が1.6以上である、
エポキシ樹脂組成物。 - 前記エポキシ化合物はビフェニル構造を有する、請求項1記載のエポキシ樹脂組成物。
- 前記エポキシ化合物と反応性の架橋性基を2個以上有する化合物(b)は、多価エポキシ化合物、多価オキセタン化合物及びポリオールからなる群より選ばれる、請求項1又は2記載のエポキシ樹脂組成物。
- (a)ビフェニル構造を有するエポキシ化合物、及び、
(b)前記エポキシ化合物と反応性の架橋性基を2個以上有する化合物、
を含むエポキシ樹脂組成物であって、
(a)/(b)の質量比が0.3〜3である、エポキシ樹脂組成物。 - ビフェニル構造を有するエポキシ化合物は単官能エポキシ化合物である、請求項4記載のエポキシ樹脂組成物。
- カチオン硬化触媒をさらに含む、請求項4又は5記載のエポキシ樹脂組成物。
- 前記エポキシ化合物と反応性の架橋性基を2個以上有する化合物(b)は、多価エポキシ化合物、多価オキセタン化合物及びポリオールからなる群より選ばれる、請求項4〜6のいずれか1項記載のエポキシ樹脂組成物。
- 請求項1〜7のいずれか1項記載の(a)及び(b)から形成されるエポキシ樹脂組成物を用いた電子機器。
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JP2009008198A JP2010163566A (ja) | 2009-01-16 | 2009-01-16 | エポキシ樹脂組成物 |
CN2010800047262A CN102282210A (zh) | 2009-01-16 | 2010-01-13 | 环氧树脂组合物 |
EP10732021A EP2387596A2 (en) | 2009-01-16 | 2010-01-13 | Epoxy resin composition |
KR1020117018680A KR20110114645A (ko) | 2009-01-16 | 2010-01-13 | 에폭시 수지 조성물 |
PCT/US2010/020864 WO2010083192A2 (en) | 2009-01-16 | 2010-01-13 | Epoxy resin composition |
US13/144,368 US20110282010A1 (en) | 2009-01-16 | 2010-01-13 | Epoxy resin composition |
TW099101134A TW201031706A (en) | 2009-01-16 | 2010-01-15 | Epoxy resin composition |
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CN (1) | CN102282210A (ja) |
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Cited By (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2012017368A (ja) * | 2010-07-06 | 2012-01-26 | Sekisui Chem Co Ltd | 光学デバイス用封止剤 |
JP2012144661A (ja) * | 2011-01-13 | 2012-08-02 | Shin-Etsu Chemical Co Ltd | アンダーフィル材及び半導体装置 |
JP2013021119A (ja) * | 2011-07-11 | 2013-01-31 | Shin Etsu Chem Co Ltd | ウエハーレベルアンダーフィル剤組成物、これを用いた半導体装置及びその製造方法 |
JP2013091676A (ja) * | 2011-10-24 | 2013-05-16 | Panasonic Corp | 新規uv硬化性樹脂組成物 |
WO2014017524A1 (ja) * | 2012-07-26 | 2014-01-30 | 電気化学工業株式会社 | 樹脂組成物 |
WO2014192839A1 (ja) | 2013-05-28 | 2014-12-04 | 株式会社ダイセル | 光半導体封止用硬化性組成物 |
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Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011062851A1 (en) | 2009-11-19 | 2011-05-26 | 3M Innovative Properties Company | Pressure sensitive adhesive comprising blend of synthetic rubber and functionalized synthetic rubber bonded to an acylic polymer |
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5993720A (ja) * | 1982-11-22 | 1984-05-30 | Showa Denko Kk | 重合性組成物 |
WO2006077862A1 (ja) * | 2005-01-24 | 2006-07-27 | Idemitsu Kosan Co., Ltd. | エポキシ樹脂組成物及びそれを用いた光学材料 |
WO2009093467A1 (ja) * | 2008-01-25 | 2009-07-30 | Mitsui Chemicals, Inc. | エポキシ重合性組成物、それを含むシール材組成物 |
JP2009227936A (ja) * | 2008-03-25 | 2009-10-08 | Nippon Shokubai Co Ltd | 硬化性樹脂組成物、その硬化物、光学部材及び光学ユニット |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06100643A (ja) * | 1992-09-22 | 1994-04-12 | Daiso Co Ltd | 重合性組成物およびそれより得られる高屈折率プラスチックレンズ |
US6297332B1 (en) * | 1998-04-28 | 2001-10-02 | Mitsui Chemicals, Inc. | Epoxy-resin composition and use thereof |
JP2002363254A (ja) * | 2001-06-06 | 2002-12-18 | Nippon Kayaku Co Ltd | エポキシ化合物、エポキシ樹脂組成物及びその硬化物 |
JP5207501B2 (ja) * | 2001-08-10 | 2013-06-12 | 日本化薬株式会社 | 光学材料用エポキシ樹脂組成物及びその硬化物 |
US6800373B2 (en) * | 2002-10-07 | 2004-10-05 | General Electric Company | Epoxy resin compositions, solid state devices encapsulated therewith and method |
CN100462385C (zh) * | 2004-03-04 | 2009-02-18 | 东亚合成株式会社 | 紫外线固化型组合物 |
JP2006083314A (ja) * | 2004-09-17 | 2006-03-30 | Toyo Ink Mfg Co Ltd | 硬化性高屈折率材料及び該硬化性高屈折率材料を用いてなる積層体 |
KR100834351B1 (ko) * | 2006-11-24 | 2008-06-02 | 제일모직주식회사 | 멀티칩 패키지 밀봉용 에폭시 수지 조성물 및 이를이용한 멀티칩 패키지 |
CN101977984B (zh) * | 2008-03-25 | 2014-03-26 | 住友电木株式会社 | 环氧树脂组合物、树脂片、半固化片、多层印刷布线板及半导体装置 |
-
2009
- 2009-01-16 JP JP2009008198A patent/JP2010163566A/ja active Pending
-
2010
- 2010-01-13 CN CN2010800047262A patent/CN102282210A/zh active Pending
- 2010-01-13 EP EP10732021A patent/EP2387596A2/en not_active Withdrawn
- 2010-01-13 WO PCT/US2010/020864 patent/WO2010083192A2/en active Application Filing
- 2010-01-13 KR KR1020117018680A patent/KR20110114645A/ko not_active Application Discontinuation
- 2010-01-13 US US13/144,368 patent/US20110282010A1/en not_active Abandoned
- 2010-01-15 TW TW099101134A patent/TW201031706A/zh unknown
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5993720A (ja) * | 1982-11-22 | 1984-05-30 | Showa Denko Kk | 重合性組成物 |
WO2006077862A1 (ja) * | 2005-01-24 | 2006-07-27 | Idemitsu Kosan Co., Ltd. | エポキシ樹脂組成物及びそれを用いた光学材料 |
WO2009093467A1 (ja) * | 2008-01-25 | 2009-07-30 | Mitsui Chemicals, Inc. | エポキシ重合性組成物、それを含むシール材組成物 |
JP2009227936A (ja) * | 2008-03-25 | 2009-10-08 | Nippon Shokubai Co Ltd | 硬化性樹脂組成物、その硬化物、光学部材及び光学ユニット |
Cited By (30)
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JP2012017368A (ja) * | 2010-07-06 | 2012-01-26 | Sekisui Chem Co Ltd | 光学デバイス用封止剤 |
JP2012144661A (ja) * | 2011-01-13 | 2012-08-02 | Shin-Etsu Chemical Co Ltd | アンダーフィル材及び半導体装置 |
JP2013021119A (ja) * | 2011-07-11 | 2013-01-31 | Shin Etsu Chem Co Ltd | ウエハーレベルアンダーフィル剤組成物、これを用いた半導体装置及びその製造方法 |
JP2013091676A (ja) * | 2011-10-24 | 2013-05-16 | Panasonic Corp | 新規uv硬化性樹脂組成物 |
WO2014017524A1 (ja) * | 2012-07-26 | 2014-01-30 | 電気化学工業株式会社 | 樹脂組成物 |
US10273389B2 (en) | 2012-07-26 | 2019-04-30 | Denka Company Limited | Resin composition |
JPWO2014017524A1 (ja) * | 2012-07-26 | 2016-07-11 | デンカ株式会社 | 樹脂組成物 |
KR20160015226A (ko) | 2013-05-28 | 2016-02-12 | 주식회사 다이셀 | 광반도체 밀봉용 경화성 조성물 |
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Also Published As
Publication number | Publication date |
---|---|
US20110282010A1 (en) | 2011-11-17 |
WO2010083192A3 (en) | 2010-10-21 |
TW201031706A (en) | 2010-09-01 |
KR20110114645A (ko) | 2011-10-19 |
WO2010083192A2 (en) | 2010-07-22 |
EP2387596A2 (en) | 2011-11-23 |
CN102282210A (zh) | 2011-12-14 |
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