JP5526511B2 - エポキシ樹脂組成物、その硬化物、硬化物の製造方法、光半導体封止用樹脂組成物、及び光半導体装置 - Google Patents
エポキシ樹脂組成物、その硬化物、硬化物の製造方法、光半導体封止用樹脂組成物、及び光半導体装置 Download PDFInfo
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- JP5526511B2 JP5526511B2 JP2008226969A JP2008226969A JP5526511B2 JP 5526511 B2 JP5526511 B2 JP 5526511B2 JP 2008226969 A JP2008226969 A JP 2008226969A JP 2008226969 A JP2008226969 A JP 2008226969A JP 5526511 B2 JP5526511 B2 JP 5526511B2
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- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- WGKLOLBTFWFKOD-UHFFFAOYSA-N tris(2-nonylphenyl) phosphite Chemical compound CCCCCCCCCC1=CC=CC=C1OP(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC WGKLOLBTFWFKOD-UHFFFAOYSA-N 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 229940070710 valerate Drugs 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
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- Polymerisation Methods In General (AREA)
- Graft Or Block Polymers (AREA)
- Epoxy Resins (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Description
本発明は、更に、前記透明性エポキシ樹脂組成物を賦型した後、加熱又は活性エネルギー線照射により硬化させることを特徴とする硬化物の製造方法に関する。
本発明は、更に、光半導体を前記透明性エポキシ樹脂組成物で封止してなることを特徴とする光半導体装置に関する。
本発明のエポキシ樹脂組成物は、前記した通り、エポキシ樹脂(A)、メタクリル酸(B)、反応性シリコーン(C)、及びラジカル重合開始剤(D)、を必須成分とするものであり、これを一度に反応させること、即ち、エポキシ基と酸基との反応と、ラジカル重合性基の重合反応とを特に反応工程として区別することなく両反応を同時乃至連続的に行うことを特徴としている。このようなイン・サイチュー反応により硬化させることにより、硬化物における耐熱黄変性と強度が飛躍的に向上することは特筆すべき点である。
ここで、上記式(2)中、R1及びR2は、それぞれ独立的にメチル基又は水素原子を表す。また、上記式(2)中、X、X’、及びX”は、それぞれ独立的に、下記構造式a〜iからなる群から選択される反応性基、又は、メチル基又は水素原子を表し、x及びyは1以上の整数である。また、x及びyの合計は2〜100となる範囲である。
一方、炭酸ジアルキルとしては反応性の点から炭酸ジメチルが挙げられる。
一方、4元系LEDの用途としては、屋外ディスプレイ、自動車のリアランプや車内照明、薄型テレビやパソコンの液晶ディスプレイのバックライト等が挙げられる。
1)ワニス粘度:25℃にてE型粘度計(東機産業(株)製「TV−20形」コーンプレートタイプを使用して測定した。
2)光線透過率:分光光度計「UV−3150」(島津製作所(株)製)を用いて測定した。
3)耐熱劣化性:150℃で72時間加熱後のエポキシ樹脂の硬化物の400nmにおける波長の光線透過率を測定した。
4)耐紫外線性:フェードメーター(スガ試験機(株)製)を使用して照射強度490W/m2、ブラックパネル温度63℃で紫外線を1000h照射した後の硬化物の400nmにおける波長の光線透過率を測定した。
5)曲げ強度、曲げ弾性率:JIS6911に準拠した。
6)貯蔵安定性:ワニスを25℃に2週間保管した後に粘度を測定した。
下記の表1又は表2に示す配合に従い、エポキシ樹脂と各種カルボン酸、重合性化合物、ラジカル重合開始剤、硬化促進剤等を、撹拌機を用いて配合してエポキシ樹脂組成物を得た。このエポキシ樹脂組成物を用いてワニス粘度、貯蔵安定性を評価した。
また、このエポキシ樹脂組成物を、厚さ3mmのスペーサー(シリコーンチューブ)をガラス板で挟んだ型の間隙に流し込み、80℃で2時間硬化させ、型から硬化物を取り出し、タックフリー状になっているのを確認した後、更に、160℃に昇温し、160℃に到達した後、該温度で2時間保持し硬化物を得、これを試験片として用い、各種の評価試験を行った。結果を表1に示す。
下記表2に示す配合に従い、各成分を配合し、撹拌機を用いて配合してエポキシ樹脂組成物を得た。このエポキシ樹脂組成物を用いてワニス粘度、貯蔵安定性を評価した。
また、このエポキシ樹脂組成物を、実施例1で用いた型の間隙に流し込み、110℃で3時間硬化させ、型から硬化物を取り出し、更に、165℃に昇温し、165℃に到達した後、該温度で2時間保持し硬化物を得、これを試験片として用い、各種の評価試験を行った。結果を表1に示す。
脂環式エポキシ樹脂 : (3,4−エポキシシクロヘキサン)メチル−3’,4’−エポキシシクロヘキシル−カルボキシレート(商品名「セロキサイド2021P」、ダイセル化学工業(株)製)
ビスフェノールA型エポキシ樹脂 : エポキシ当量188g/eq.のビスフェノールA型エポキシ樹脂(商品名「EPICLON 850S」、DIC(株)製)
水添ビスフェノールA型エポキシ樹脂 : 水添ビスフェノールA型エポキシ樹脂(商品名「EPICLON EXA−7015」エポキシ当量200g/eq.、DIC(株)製)
HO−MS : 3‐[[2‐(メタクリロイルオキシ)エトキシ]カルボニル]プロピオン酸(商品名「ライトエステルHO−MS」、共栄社化学(株)製)
HO−HH : 2−メタクリロイルオキシエチルヘキサヒドロフタル酸(商品名「ライトエステルHO−HH」、共栄社化学(株)製))
ジシクロペンタニルメタクリレート : 商品名「ファンクリルFA−513M」日立化成工業(株)製
反応性シリコーン1 メタクリル基含有シリコーンオイル(信越化学製、商品名「X−22−2475」、粘度(25℃)5mm2/s、比重(25℃)0.93、屈折率(25℃)1.418、官能基当量420g/モル)
反応性シリコーン2 メタクリル基含有シリコーンオイル(信越化学製、商品名「X−22−164A」、粘度(25℃)25mm2/s、比重(25℃)0.98、屈折率(25℃)1.415、官能基当量860g/モル)
過酸化物 : 1,1−ジ(t−ヘキシルペルオキシ)シクロヘキサン(商品名「パーヘキサHC」日油(株)製))
硬化促進剤 : メチルトリブチルホスホニウムジメチルホスフェート(商品名「ヒシコーリンPX−4MP」日本化学工業(株)製))
Claims (14)
- エポキシ樹脂(A)、メタクリル酸(B)、シリコーン(C)、及び熱ラジカル重合開始剤(D)を必須成分とするエポキシ樹脂組成物であって、
前記シリコーン(C)が、ポリシロキサン構造にアミノ基、エポキシ基、脂環式エポキシ基、カルビノール系水酸基、シラノール系水酸基、メタクリロイル基、アクリロイル基、ポリエーテルアルコール基、メルカプト基、及びカルボキシル基から選択される官能基を含むものであることを特徴とするエポキシ樹脂組成物。 - エポキシ樹脂(A)、メタクリル酸(B)、及びシリコーン(C)の合計100質量部のうち、前記エポキシ樹脂(A)を10〜60質量部、前記メタクリル酸(B)を1〜30質量部、及びシリコーン(C)を20〜80質量部となる割合で含有する請求項1に記載のエポキシ樹脂組成物。
- 上記エポキシ樹脂(A)、メタクリル酸(B)、シリコーン(C)、及び熱ラジカル重合開始剤(D)に加え、脂肪族エステル結合又は脂肪族カーボネート結合を有する酸基含有ラジカル重合性単量体(E)を含有する請求項1又は2記載のエポキシ樹脂組成物。
- エポキシ樹脂(A)、メタクリル酸(B)、シリコーン(C)、及び脂肪族エステル結合又は脂肪族カーボネート結合を有する酸基含有ラジカル重合性単量体(E)の合計100質量部のうち、前記エポキシ樹脂(A)を10〜60質量部、前記メタクリル酸(B)を1〜30質量部、シリコーン(C)を15〜70質量部、前記脂肪族エステル結合又は脂肪族カーボネート結合を有する酸基含有ラジカル重合性単量体(E)を5〜30質量部となる割合で含有する請求項3又は4記載のエポキシ樹脂組成物。
- エポキシ樹脂(A)、メタクリル酸(B)、シリコーン(C)、脂肪族エステル結合又は脂肪族カーボネート結合を有する酸基含有ラジカル重合性単量体(E)、及び熱ラジカル重合開始剤(D)の各成分に加え、脂肪族環状構造含有モノメタクリレート化合物(F)を含有する請求項3〜5の何れか1つに記載のエポキシ樹脂組成物。
- エポキシ樹脂(A)、メタクリル酸(B)、シリコーン(C)、脂肪族エステル結合又は脂肪族カーボネート結合を有する酸基含有ラジカル重合性単量体(E)、及び熱ラジカル重合開始剤(D)の合計質量100質量部に対して、前記脂肪族環状構造含有モノメタクリレート化合物(F)を47.1〜55.0質量部となる割合で含有するエポキシ樹脂組成物であって、
前記脂肪族エステル結合又は脂肪族カーボネート結合を有する酸基含有ラジカル重合性単量体(E)が、下記構造式(1)
前記脂肪族環状構造含有モノメタクリレート化合物(F)が、ジシクロペンタニルメタクリレート、ジシクロペンテニルオキシエチルメタクリレート、1,2−エポキシ−4−ビニルシクロヘキサン、3,4−エポキシシクロヘキシルメチルメタアクリレート、シクロヘキシルメタクリレート、2−メチルシクロヘキシルメタクリレート、イソボニルメタクリレートからなる群から選択される少なくとも1種の化合物である請求項6記載のエポキシ樹脂組成物。 - 前記エポキシ樹脂(A)が、環状脂肪族構造を有するエポキシ樹脂である請求項1〜7の何れか1つに記載のエポキシ樹脂組成物。
- 前記エポキシ樹脂(A)が、エポキシ当量150〜1,000g/eq.のビスフェノール型エポキシ樹脂である請求項1〜7の何れか1つに記載のエポキシ樹脂組成物。
- 請求項1〜9の何れか1つに記載のエポキシ樹脂組成物からなることを特徴とする光半導体封止用樹脂組成物。
- 高輝度LED素子封止用材料である請求項10記載の組成物。
- 請求項1〜9の何れか1つに記載のエポキシ樹脂組成物を賦型した後、イン・サイチュー反応により硬化させてなる硬化物。
- 請求項1〜9の何れか1つに記載のエポキシ樹脂組成物を成形機内でイン・サイチュー反応により硬化させることを特徴とする硬化物の製造方法。
- 光半導体を請求項1〜9の何れか1つに記載のエポキシ樹脂組成物で封止してなることを特徴とする光半導体装置。
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