JP6018704B2 - 感光性樹脂組成物および前記感光性樹脂組成物から製造されたベゼルパターンを含むタッチパネル - Google Patents
感光性樹脂組成物および前記感光性樹脂組成物から製造されたベゼルパターンを含むタッチパネル Download PDFInfo
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- JP6018704B2 JP6018704B2 JP2015514890A JP2015514890A JP6018704B2 JP 6018704 B2 JP6018704 B2 JP 6018704B2 JP 2015514890 A JP2015514890 A JP 2015514890A JP 2015514890 A JP2015514890 A JP 2015514890A JP 6018704 B2 JP6018704 B2 JP 6018704B2
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- 239000010409 thin film Substances 0.000 description 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- 239000005341 toughened glass Substances 0.000 description 1
- HTSABYAWKQAHBT-UHFFFAOYSA-N trans 3-methylcyclohexanol Natural products CC1CCCC(O)C1 HTSABYAWKQAHBT-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- YFNKIDBQEZZDLK-UHFFFAOYSA-N triglyme Chemical compound COCCOCCOCCOC YFNKIDBQEZZDLK-UHFFFAOYSA-N 0.000 description 1
- NMEPHPOFYLLFTK-UHFFFAOYSA-N trimethoxy(octyl)silane Chemical compound CCCCCCCC[Si](OC)(OC)OC NMEPHPOFYLLFTK-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 150000007964 xanthones Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 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
- G03F7/004—Photosensitive materials
- G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
- G03F7/032—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with binders
- G03F7/033—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with binders the binders being polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. vinyl polymers
-
- 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
- G03F7/004—Photosensitive materials
-
- 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
- G03F7/004—Photosensitive materials
- G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
- G03F7/032—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with binders
-
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06F—ELECTRIC DIGITAL DATA PROCESSING
- G06F3/00—Input arrangements for transferring data to be processed into a form capable of being handled by the computer; Output arrangements for transferring data from processing unit to output unit, e.g. interface arrangements
- G06F3/01—Input arrangements or combined input and output arrangements for interaction between user and computer
- G06F3/03—Arrangements for converting the position or the displacement of a member into a coded form
- G06F3/041—Digitisers, e.g. for touch screens or touch pads, characterised by the transducing means
-
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06F—ELECTRIC DIGITAL DATA PROCESSING
- G06F3/00—Input arrangements for transferring data to be processed into a form capable of being handled by the computer; Output arrangements for transferring data from processing unit to output unit, e.g. interface arrangements
- G06F3/01—Input arrangements or combined input and output arrangements for interaction between user and computer
- G06F3/03—Arrangements for converting the position or the displacement of a member into a coded form
- G06F3/041—Digitisers, e.g. for touch screens or touch pads, characterised by the transducing means
- G06F3/0412—Digitisers structurally integrated in a display
-
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06F—ELECTRIC DIGITAL DATA PROCESSING
- G06F2203/00—Indexing scheme relating to G06F3/00 - G06F3/048
- G06F2203/041—Indexing scheme relating to G06F3/041 - G06F3/045
- G06F2203/04103—Manufacturing, i.e. details related to manufacturing processes specially suited for touch sensitive devices
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24777—Edge feature
- Y10T428/24793—Comprising discontinuous or differential impregnation or bond
Landscapes
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Theoretical Computer Science (AREA)
- General Engineering & Computer Science (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Human Computer Interaction (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials For Photolithography (AREA)
- Graft Or Block Polymers (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Polymerisation Methods In General (AREA)
- Adhesives Or Adhesive Processes (AREA)
Description
Rxは、C1〜C10のアルキレン基;C1〜C5のアルキル基で置換もしくは非置換されたC3〜C10のシクロアルキレン基;C1〜C5のアルキル基で置換もしくは非置換されたC6〜C10のアリーレン基;またはC1〜C5のアルキル基で置換もしくは非置換された−NH−R−NH−であり、
Rは、C1〜C10のアルキレン基;C1〜C5のアルキル基で置換もしくは非置換されたC3〜C20のシクロアルキレン基;またはC1〜C5のアルキル基で置換もしくは非置換されたC6〜C10のアリーレン基であり、
Ryは、水素、アクリロイルまたはメタアクリロイルであり、
nは、1〜5,000の整数である。
カーボン分散液(トクシキ社製、BK_8115、カーボン含量20%)600g、アルカリ可溶性アクリル系バインダー1としてベンジルメタクリレート/N−フェニルマレイミド/スチレン/グリシジルメタクリレートが付加されたメタクリル酸/メタクリル酸{(モル比38/7/7/17/31、Mw=9000、124KOHmg/g)、固形分含量30%}70g、アクリル系バインダー2としてベンジルメタクリレート/N−フェニルマレイミド/スチレン/ラウリルメタクリレート/メタクリル酸{(モル比44/7/8/14/27、Mw=19000、105KOHmg/g)、固形分含量30%}130g、多官能性モノマーとしてジペンタエリスリトールヘキサアクリレート35g、光重合開始剤としてN−1919(アデカ社製)20g、密着促進剤として3−メタアクリルオキシプロピルトリメトキシシラン5gおよびレベリング剤としてF−475(DIC社製)1g、溶媒としてプロピレングリコールモノメチルエーテルアセテート530g、3−メトキシブチルアセテート100gを混合した。
カーボン分散液(トクシキ社製、BK_8115、カーボン含量20%)600g、アルカリ可溶性アクリル系バインダー1としてベンジルメタクリレート/N−フェニルマレイミド/スチレン/グリシジルメタクリレートが付加されたメタクリル酸/メタクリル酸{(モル比38/7/7/17/31、Mw=9000、124KOHmg/g)、固形分含量30%}70g、アクリル系バインダー2としてベンジルメタクリレート/N−フェニルマレイミド/スチレン/ラウリルメタクリレート/メタクリル酸{(モル比44/7/8/14/27、Mw=19000、105KOHmg/g)、固形分含量30%}100g、フルオレン系バインダー{アクリル酸が付加されたビスフェノールフルオレンエポキシアクリレート/1,3−シクロヘキシルジイソシアネート(モル比65/35、Mw=5000、酸価80KOHmg/g)固形分含量35%}30g、多官能性モノマーとしてジペンタエリスリトールヘキサアクリレート35g、光重合開始剤としてN−1919(アデカ社製)20g、密着促進剤として3−メタアクリルオキシプロピルトリメトキシシラン5gおよびレベリング剤としてF−475(DIC社製)1g、溶媒としてプロピレングリコールモノメチルエーテルアセテート530g、3−メトキシブチルアセテート100gを混合した。
カーボン分散液(トクシキ社製、BK_8115、カーボン含量20%)600g、アルカリ可溶性アクリル系バインダーとしてベンジルメタクリレート/N−フェニルマレイミド/スチレン/ラウリルメタクリレート/グリシジルメタクリレートが付加されたメタクリル酸/メタクリル酸{(モル比35/7/7/14/12/25、Mw=18000、105KOHmg/g)、固形分含量30%}150g、フルオレン系バインダー{アクリル酸が付加されたビスフェノールフルオレンエポキシアクリレート/1,3−シクロヘキシルジイソシアネート(モル比65/35、Mw=5000、酸価80KOHmg/g)固形分含量35%}40g、多官能性モノマーとしてジペンタエリスリトールヘキサアクリレート35g、光重合開始剤としてN−1919(アデカ社製)20g、密着促進剤として3−メタアクリルオキシプロピルトリメトキシシラン5gおよびレベリング剤としてF−475(DIC社製)1g、溶媒としてプロピレングリコールモノメチルエーテルアセテート530g、3−メトキシブチルアセテート100gを混合した
カーボン分散液(トクシキ社製、BK_8115、カーボン含量20%)600g、アルカリ可溶性アクリル系バインダーとしてベンジルメタクリレート/N−フェニルマレイミド/スチレン/グリシジルメタクリレートが付加されたメタクリル酸/メタクリル酸{(モル比38/7/7/17/31、Mw=15000、124KOHmg/g)、固形分含量30%}200g、多官能性モノマーとしてジペンタエリスリトールヘキサアクリレート35g、光重合開始剤としてN−1919(アデカ社製)20g、密着促進剤として3−メタアクリルオキシプロピルトリメトキシシラン5重量部およびレベリング剤としてF−475(DIC社製)1g、溶媒としてプロピレングリコールモノメチルエーテルアセテート530g、3−メトキシブチルアセテート100gを混合した。
カーボン分散液(トクシキ社製、BK_8115、カーボン含量20%)600g、アルカリ可溶性アクリル系バインダーとしてベンジルメタクリレート/ラウリルメタクリレート/グリシジルメタクリレートが付加されたメタクリル酸/メタクリル酸{(モル比30/35/8/27、Mw=13000、105KOHmg/g)、固形分含量30%}200g、多官能性モノマーとしてジペンタエリスリトールヘキサアクリレート35g、光重合開始剤としてN−1919(アデカ社製)20g、密着促進剤として3−メタアクリルオキシプロピルトリメトキシシラン5重量部およびレベリング剤としてF−475(DIC社製)1g、溶媒としてプロピレングリコールモノメチルエーテルアセテート530g、3−メトキシブチルアセテート100gを混合した。
その次、前記混合物を5時間攪拌して感光性樹脂組成物を製造した。
カーボン分散液(トクシキ社製、BK_8115、カーボン含量20%)600g、アルカリ可溶性アクリル系バインダー1としてベンジルメタクリレート/N−フェニルマレイミド/スチレン/グリシジルメタクリレートが付加されたメタクリル酸/メタクリル酸{(モル比38/7/7/17/31、Mw=9000、124KOHmg/g)、固形分含量30%}50g、アクリル系バインダー2としてベンジルメタクリレート/N−フェニルマレイミド/スチレン/ラウリルメタクリレート/メタクリル酸{(モル比44/7/8/14/27、Mw=19000、105KOHmg/g)、固形分含量30%}50g、フルオレン系バインダー{アクリル酸が付加されたビスフェノールフルオレンエポキシアクリレート/1,3−シクロヘキシルジイソシアネート(モル比65/35、Mw=5000、酸価80KOHmg/g)固形分含量35%}100g、多官能性モノマーとしてジペンタエリスリトールヘキサアクリレート35g、光重合開始剤としてN−1919(アデカ社製)20g、密着促進剤として3−メタアクリルオキシプロピルトリメトキシシラン5gおよびレベリング剤としてF−475(DIC社製)1g、溶媒としてプロピレングリコールモノメチルエーテルアセテート530g、3−メトキシブチルアセテート100gを混合した。
その次、前記混合物を5時間攪拌して感光性樹脂組成物を製造した。
実施例1〜3および比較例1〜3の感光性樹脂組成物をガラスにスピンコーティングを用いてコーティングした後、約100℃で2分間前熱処理して約1.42μm厚さの塗膜を形成した。その次、室温で冷却した後、フォトマスクを用いて高圧水銀ランプ下で100mJ/cm2のエネルギーで露光させた。前記露光された基板を25℃の温度で0.04%のKOH水溶液においてスプレー方式で現像した後、純水で洗浄して乾燥し、230℃の対流式オーブンで20分間ポストベーク(post−bake)を行った。
Claims (12)
- 基板、および前記基板上に感光性樹脂組成物から製造されたベゼル(bezel)パターンを含むタッチパネルであって、
前記感光性樹脂組成物は、
アクリル系バインダーを含むバインダー樹脂;重合性化合物;開始剤;および溶媒を含み、
前記アクリル系バインダーを構成するモノマーは、不飽和結合を含む化合物、側鎖が長い化合物、および酸基を含む化合物を含み、
前記側鎖が長い化合物は、エチレン性不飽和結合を有し、側鎖に置換された炭素数が8〜18のアルキル鎖を有し、
前記モノマーの総モル数を基準に、前記側鎖が長い化合物の含量は1〜30モル%であるタッチパネル。 - 前記バインダー樹脂の総重量を基準に、前記アクリル系バインダーの含量は50〜90重量%である請求項1に記載のタッチパネル。
- 前記バインダー樹脂は、不飽和結合を含む化合物および酸基を含む化合物から重合された追加のアクリル系バインダーをさらに含む請求項1または2に記載のタッチパネル。
- 前記バインダー樹脂は、下記化学式1で表される繰り返し単位を有するフルオレン系バインダーをさらに含む請求項1〜3のうちいずれか1項に記載のタッチパネル:
[化学式1]
前記化学式1において、
Rxは、C1〜C10のアルキレン基;C1〜C5のアルキル基で置換もしくは非置換されたC3〜C10のシクロアルキレン基;C1〜C5のアルキル基で置換もしくは非置換されたC6〜C10のアリーレン基;またはC1〜C5のアルキル基で置換もしくは非置換された−NH−R−NH−であり、
Rは、C1〜C10のアルキレン基;C1〜C5のアルキル基で置換もしくは非置換されたC3〜C20のシクロアルキレン基;またはC1〜C5のアルキル基で置換もしくは非置換されたC6〜C10のアリーレン基であり、
Ryは、水素、アクリロイルまたはメタアクリロイルであり、
nは、1〜5,000の整数である。 - 前記バインダー樹脂の総重量を基準に、前記アクリル系バインダーの含量は50重量%以上90重量%未満であり、前記フルオレン系バインダーの含量は10〜50重量%である請求項4に記載のタッチパネル。
- 前記感光性樹脂組成物は着色剤をさらに含む請求項1〜5のうちいずれか1項に記載のタッチパネル。
- 前記着色剤の表面抵抗値は1012Ω/square以上である請求項6に記載のタッチパネル。
- 前記感光性樹脂組成物の総重量を基準に、前記バインダー樹脂の含量は1〜20重量%であり、前記重合性化合物の含量は1〜10重量%であり、前記着色剤の含量は5〜30重量%であり、前記開始剤の含量は0.1〜10重量%であり、前記溶媒の含量は60〜90重量%である請求項6または7に記載のタッチパネル。
- 前記ベゼルパターンのテーパー角は0°超過60°以下である請求項1から8のいずれか1項に記載のタッチパネル。
- 前記ベゼルパターンの厚さは0.3μm〜5μmである請求項1から9のいずれか1項に記載のタッチパネル。
- 前記ベゼルパターンの表面抵抗値は1012Ω/square以上である請求項1から10のうちいずれか1項に記載のタッチパネル。
- 前記ベゼルパターンの厚さ1μm当たりの光学密度は1〜5である請求項1から11のうちいずれか1項に記載のタッチパネル。
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KR101521775B1 (ko) * | 2013-12-20 | 2015-05-20 | 주식회사 엘엠에스 | 굴절률 매칭용 조성물, 이를 이용하여 제조된 터치스크린 기판 및 표시장치 |
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KR102202975B1 (ko) | 2014-07-09 | 2021-01-14 | 동우 화인켐 주식회사 | 후막 패턴 구조 및 그의 형성 방법 |
KR102212674B1 (ko) * | 2014-07-09 | 2021-02-05 | 동우 화인켐 주식회사 | 후막 패턴 구조 및 그의 형성 방법 |
US10723900B2 (en) * | 2014-10-21 | 2020-07-28 | Lg Chem, Ltd. | UV curable ink for inkjet, method for manufacturing a bezel using the same, a bezel pattern using the same method and display panel comprising the bezel pattern |
KR20160117817A (ko) * | 2015-03-31 | 2016-10-11 | 삼성디스플레이 주식회사 | 화소 및 이를 이용한 표시 장치 |
JP6700710B2 (ja) * | 2015-10-16 | 2020-05-27 | 日鉄ケミカル&マテリアル株式会社 | ブラックカラムスペーサー用の感光性樹脂組成物、ブラックカラムスペーサー、液晶表示装置、ブラックカラムスペーサー用の感光性樹脂組成物の製造方法、ブラックカラムスペーサーの製造方法、および液晶表示装置の製造方法 |
WO2017110893A1 (ja) * | 2015-12-24 | 2017-06-29 | 三菱化学株式会社 | 感光性着色組成物、硬化物、着色スペーサー、画像表示装置 |
KR102067857B1 (ko) | 2016-04-08 | 2020-01-17 | 주식회사 엘지화학 | 잉크젯 프린팅을 이용한 베젤 패턴의 형성 방법 |
KR102054045B1 (ko) * | 2017-03-03 | 2019-12-09 | 주식회사 엘지화학 | 고분자 수지 화합물 및 이를 포함하는 블랙 뱅크용 감광성 수지 조성물 |
KR102333186B1 (ko) | 2018-08-17 | 2021-11-29 | 주식회사 엘지화학 | 필름 인쇄 가능한 자외선 경화형 잉크 조성물, 이를 이용한 베젤패턴의 제조방법, 이에 따라 제조한 베젤패턴 및 이를 포함하는 디스플레이 기판 |
Family Cites Families (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2038785C (en) * | 1990-03-27 | 1998-09-29 | Atsushi Oyamatsu | Magneto-optical recording medium |
KR19980068288A (ko) * | 1997-02-17 | 1998-10-15 | 한형수 | 불포화기와 감광기를 동시에 함유하는 감광성수지조성물 및 착색조성물 |
KR19990015097A (ko) * | 1997-08-01 | 1999-03-05 | 한형수 | 광개시제 성분을 측쇄에 함유하는 감광성 수지조성물 |
TWI285297B (en) * | 2004-02-09 | 2007-08-11 | Chi Mei Corp | Light-sensitive resin composition for black matrix |
US20060166114A1 (en) | 2004-06-21 | 2006-07-27 | Chun-Hsien Lee | Photosensitive resin composition for black matrix |
KR20130042049A (ko) | 2004-07-14 | 2013-04-25 | 아사히 가세이 이-매터리얼즈 가부시키가이샤 | 감광성 조성물, 패턴형성재료, 감광성 적층체, 및 패턴형성장치 및 패턴형성방법 |
KR100731325B1 (ko) * | 2005-06-23 | 2007-06-25 | 주식회사 삼양이엠에스 | 음성 레지스트 조성물 |
KR100791817B1 (ko) | 2005-09-30 | 2008-01-04 | 주식회사 동진쎄미켐 | 감광성 수지 조성물 |
JP5255783B2 (ja) * | 2006-06-01 | 2013-08-07 | 新日鉄住金化学株式会社 | カラーフィルター用レジスト組成物及びその製造方法並びにそれを用いたカラーフィルター |
CN101657414A (zh) * | 2007-01-23 | 2010-02-24 | 富士胶片株式会社 | 肟化合物、感光性组合物、滤色片及其制造方法以及液晶显示元件 |
JP2008304527A (ja) * | 2007-06-05 | 2008-12-18 | Hitachi Chem Co Ltd | 感光性樹脂組成物、これを用いた感光性エレメント、レジストパターンの形成方法及びプリント配線板の製造方法 |
KR101032275B1 (ko) | 2007-11-08 | 2011-05-06 | 주식회사 엘지화학 | 착색 분산액, 감광성 수지조성물 및 블랙매트릭스 |
JP2010032683A (ja) * | 2008-07-28 | 2010-02-12 | Toppan Printing Co Ltd | 着色アルカリ現像型感光性樹脂組成物及びカラーフィルタ |
JP5669386B2 (ja) * | 2009-01-15 | 2015-02-12 | 富士フイルム株式会社 | 新規化合物、重合性組成物、カラーフィルタ、及びその製造方法、固体撮像素子、並びに、平版印刷版原版 |
KR101208893B1 (ko) * | 2009-08-04 | 2012-12-07 | 롬엔드하스전자재료코리아유한회사 | 초소수성 감광성 수지조성물 및 이를 이용한 블랙매트릭스 |
JP5458848B2 (ja) * | 2009-12-08 | 2014-04-02 | 株式会社リコー | 電子写真感光体、画像形成装置及びプロセスカートリッジ |
KR101068622B1 (ko) | 2009-12-22 | 2011-09-28 | 주식회사 엘지화학 | 기판접착력이 향상된 고차광성 블랙매트릭스 조성물 |
KR101140954B1 (ko) * | 2010-05-13 | 2012-05-03 | 삼성전기주식회사 | 투명 전도성 기판과 그 제조방법, 및 이를 이용한 터치스크린 |
JP5966278B2 (ja) * | 2010-08-26 | 2016-08-10 | 住友大阪セメント株式会社 | 黒色膜、黒色膜付き基材及び画像表示装置、並びに黒色樹脂組成物及び黒色材料分散液 |
CN103069316B (zh) * | 2010-08-26 | 2015-09-09 | 住友大阪水泥股份有限公司 | 黑色膜、带黑色膜的基材和图像显示装置以及黑色树脂组合物和黑色材料分散液 |
KR101367253B1 (ko) * | 2010-10-13 | 2014-03-13 | 제일모직 주식회사 | 감광성 수지 조성물 및 이를 이용한 차광층 |
KR101333712B1 (ko) * | 2010-10-22 | 2013-11-27 | 제일모직주식회사 | 감광성 수지 조성물 및 이를 이용한 컬러필터 |
TWI564661B (zh) * | 2012-05-25 | 2017-01-01 | Lg化學股份有限公司 | 光敏樹脂組成物、使用其形成之圖案以及包含其之顯示面板 |
KR20140066417A (ko) * | 2012-11-23 | 2014-06-02 | 삼성전기주식회사 | 터치 스크린 모듈 및 이의 제조방법 |
KR101709698B1 (ko) * | 2013-09-02 | 2017-02-23 | 제일모직 주식회사 | 흑색 감광성 수지 조성물 및 이를 이용한 차광층 |
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US9470975B2 (en) | 2016-10-18 |
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