JP5668118B2 - 感光性樹脂組成物及び硬化膜 - Google Patents
感光性樹脂組成物及び硬化膜 Download PDFInfo
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- JP5668118B2 JP5668118B2 JP2013195770A JP2013195770A JP5668118B2 JP 5668118 B2 JP5668118 B2 JP 5668118B2 JP 2013195770 A JP2013195770 A JP 2013195770A JP 2013195770 A JP2013195770 A JP 2013195770A JP 5668118 B2 JP5668118 B2 JP 5668118B2
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- 229950000688 phenothiazine Drugs 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920000767 polyaniline Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
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- 230000003068 static effect Effects 0.000 description 1
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- QJVXKWHHAMZTBY-GCPOEHJPSA-N syringin Chemical compound COC1=CC(\C=C\CO)=CC(OC)=C1O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 QJVXKWHHAMZTBY-GCPOEHJPSA-N 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 150000000000 tetracarboxylic acids Chemical class 0.000 description 1
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Images
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- Optical Filters (AREA)
- Exposure And Positioning Against Photoresist Photosensitive Materials (AREA)
- Materials For Photolithography (AREA)
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Description
本発明の組成物は、(イ)及び(ロ)成分を必須成分として含有し、遮光性の硬化膜を得る場合には更に(ハ)成分を含めて必須成分とする。ここで、(イ)成分である光硬化性樹脂は、例えば、次のような不飽和基含有化合物であることが好ましい。すなわちビスフェノール類から誘導される2個のグリシジルエーテル基を有するエポキシ化合物に、(メタ)アクリル酸(これは「アクリル酸及び/又はメタクリル酸」の意味である)を反応させ、得られたヒドロキシ基を有する化合物に多塩基酸カルボン酸又はその無水物を反応させて得られるエポキシ(メタ)アクリレート酸付加物である。ここで、ビスフェノール類から誘導されるエポキシ化合物とは、ビスフェノール類とエピハロヒドリンを反応させて得られるエポキシ化合物を意味する。かかるエポキシ化合物及び該エポキシ化合物より誘導される不飽和基含有化合物(エポキシ(メタ)アクリレート酸付加物)は、前記特許文献2等により公知であり、かかる化合物が広く使用できる。
アクリル樹脂粒子(日本ペイント社製ファインスフェア)、高分子分散剤及びプロピレングリコールモノメチルエーテルアセテートを表1に示す割合に混合し、ビーズミルにて分散を行い、アクリル樹脂粒子を含有する分散液A-1〜A-4、及びa-1を調製した。また、アクリル樹脂粒子(日本ペイント社製ファインスフェア)、遮光性顔料(遮光性成分)として樹脂被覆カーボンブラック(三菱化学社製MS18E、粒径25nm)、高分子分散剤及びプロピレングリコールモノメチルエーテルアセテートを表1に示す割合に混合し、ビーズミルにて分散を行い、アクリル樹脂粒子/遮光性顔料を双方とも含有する分散液A-5とした。同様に、遮光性顔料としてカーボンブラックにかえて、チタンブラック(三菱マテリアル製、粒径30nm)もしくは混色有機顔料ブラック(御国色素製、粒径30nm)を用いてアクリル樹脂粒子/遮光性顔料を双方とも含有する分散液A-6〜A-7を調製した。製造番号9の分散液a-2はアクリル樹脂粒子を配合せず、遮光性顔料として樹脂被服カーボンブラック(三菱化学社製MS18E、粒径25nm)のみを含有した分散液とした。なお、製造番号1〜8で使用したアクリル樹脂粒子は、いずれも単一組成のアクリル樹脂(単核組成)を球状となるように制御して製造されたものであり、一次粒子径の平均値は表1に示したとおりである。また、製造番号1、4〜8のものは粒子表面に酸性官能基が存在するように表面を処理したものであり、製造番号3のものは粒子表面に塩基性官能基が存在するように表面を処理したものであり、製造番号2は、表面無処理のものである。なお、粒子の一次粒子径の平均値は、透過型電子顕微鏡により粒径観察を行ない、無作為に100個の粒子を選定して粒子の長軸長と短軸長を計測し、これらの相加平均により求めた。その際、凝集塊やアグリゲイトを構成している場合には、一次粒子とはこれらを構成する粒子を指すものとした。
<隔壁用感光性樹脂組成物の調製>
上記で得た分散液と表2記載の各成分とをそれぞれ表中に示した割合で混合した上で、シランカップリング剤S-510(信越化学製)0.30部とともにプロピレングリコールモノメチルエーテルアセテートを加えて全量100重量部、固形分濃度20重量%とした。さらにシリコン系界面活性剤SH3775M(東レ・ダウコーニング製)0.005重量部を加えて、2μmのポリプロピレン製メンブレンフィルターを用いて0.2kg/cm2加圧にてろ過し、感光性樹脂組成物を調製した。なお、表2中に記載した各成分の略号はそれぞれ以下のものを表す。
B-1:フルオレン骨格を有するエポキシアクリレートの酸無水物重縮合物のプロピレングリコールモノメチルエーテルアセテート溶液(樹脂固形分濃度=56.1重量%、新日鐵化学社製 商品名V259ME)
C-1:ジペンタエリスリトールヘキサアクリレートとジペンタエリスリトールペンタアクリレートとの混合物(日本化薬社製 商品名 DPHA)
C-2:トリメチロールプロパントリアクリレート(巴工業製 商品名 SARTOMER SR-351S)
D-1:光重合開始剤、IRGACURE OXE01(チバ・ジャパン製)
D-2:光重合開始剤、IRGACURE OXE02(チバ・ジャパン製)
スピンコート後の塗膜に放射状スジが観察された場合を×<不良>、観察されなかった場合を○<良好>とした。
[感度]
ステップマスクを用いて、BT(ブレイクタイム)+20秒にて残膜が観測される露光量(mj/cm2)を測定した。
[現像密着性]
BT(ブレイクタイム)+40秒において20μmパターンが残っている場合を○、剥離したものを×とした。
[パターン直線性]
ポストベーク後の20μmラインを顕微鏡で観察し、ギザツキが観測された場合を×、ない場合を○とした。また、局所的にギザツキが観測される場合を△とした。
[膜厚ならびに表面粗度(表面粗さRa:JIS B0601-1994)]
触針式膜厚計(テンコール(株)製)を用いて測定した。表面粗度はブラックマトリックス表面上2mm幅に置けるRa(Å)とし、150Å未満を○、150Åを超える場合を×とした。
[テーパ形状]
現像時間が抜け時間+10〜30秒において、ポストベーク後の20μmライン断面を操作型電子顕微鏡で観察し、基板と構造物(硬化膜)テーパ部のなす角度が常に60°以上を○、60°未満を△、円弧形状(図2、(b))の場合を×とした。
[体積抵抗値]
全面にクロム蒸着したガラス基板上に前述と同様にしてポストベーク後2.1μm膜厚の塗膜を形成した。塗膜上に10mmφのAl蒸着膜を形成し、Cr−Al間に1〜10Vの電圧を印加し、電流値を測定して、抵抗を求めた。
[OD測定]
ポストベーク後2.1μmの塗膜を用いて、大塚電子製OD計を用いて測定、1μmあたりのOD値として記載した。
実施例6〜11で用いた感光性樹脂組成物を用い、開口部(画素領域)が300μm×100μmであり、尚且つ、ライン幅が30μm、膜厚(高さ)2.1μmの遮光性隔壁を有するマトリックスを形成した。その後、酸素大気圧プラズマで3秒間処理した後に、CF4大気圧プラズマにて3秒間処理を行った。この遮光性隔壁(遮光膜)上に水またはブチルカルビトールアセテート(BCA)を用いて、静的接触角を測定したところ、それぞれ100°、50°を示した。このブラックマトリックス中にむかって、東芝テック製インクジェットヘッドを用い、粘度9mPa・sec、固形分濃度20%のレッド、ブルー、グリーンのインキを打ち込み、230℃にてポストベークを行い、カラーフィルターを形成した。その結果、良好なカラーフィルターを得ることができた。
2:塗膜
2a:塗膜の硬化部分
3:硬化後の塗膜の理想形状
Claims (5)
- (イ)光硬化性樹脂及び/又は光硬化性単量体と、(ロ)アクリル樹脂粒子とを必須成分とし、更に(ハ)黒色有機顔料、混色有機顔料及び遮光材から選ばれる少なくとも1種の遮光性成分とを含有してなる感光性樹脂組成物であって、(ロ)成分のアクリル樹脂粒子が表面酸処理されたアクリル樹脂粒子であると共に、一次粒子径の平均値が50〜200nmであり、前記組成物中のアクリル樹脂粒子(ロ)、及び遮光性成分(ハ)の総重量と光硬化性樹脂及び/又は光硬化性単量体(イ)との重量比((ロ)+(ハ)/(イ))が0.1〜2.0の範囲であることを特徴とする感光性樹脂組成物。
- (ハ)成分の遮光性成分がカーボンブラックである請求項1に記載の感光性樹脂組成物。
- 請求項1〜3のいずれかに記載の感光性樹脂組成物を基板上に塗布、乾燥した後、(a)紫外線露光装置による露光、(b)アルカリ水溶液による現像、及び(c)熱処理の各工程を必須として得られる硬化膜。
- 体積抵抗値が1010Ωcm以上である請求項4に記載の硬化膜。
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