JP2007112919A - 顔料分散液、着色剤組成物、およびカラーフィルター - Google Patents
顔料分散液、着色剤組成物、およびカラーフィルター Download PDFInfo
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- JP2007112919A JP2007112919A JP2005306685A JP2005306685A JP2007112919A JP 2007112919 A JP2007112919 A JP 2007112919A JP 2005306685 A JP2005306685 A JP 2005306685A JP 2005306685 A JP2005306685 A JP 2005306685A JP 2007112919 A JP2007112919 A JP 2007112919A
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| JP2010002550A (ja) * | 2008-06-19 | 2010-01-07 | Toray Ind Inc | カラーフィルター用緑色着色剤組成物、およびカラーフィルター |
| JP2010044981A (ja) * | 2008-08-15 | 2010-02-25 | Fujifilm Corp | 表示装置 |
| JP2010180376A (ja) * | 2009-02-09 | 2010-08-19 | Fujifilm Corp | インク組成物、及び、インクジェット記録方法 |
| WO2012153669A1 (en) * | 2011-05-10 | 2012-11-15 | Canon Kabushiki Kaisha | Pigment dispersion, ink composition including pigment dispersion, and color filter yellow resist composition including pigment dispersion |
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Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH09122470A (ja) * | 1995-10-28 | 1997-05-13 | Sanyo Shikiso Kk | 顔料分散剤 |
| JP2001188120A (ja) * | 2000-01-05 | 2001-07-10 | Toray Ind Inc | カラーフィルター用着色組成物、およびそれを使用したカラーフィルター、液晶表示装置 |
| JP2004163487A (ja) * | 2002-11-11 | 2004-06-10 | Toyo Ink Mfg Co Ltd | カラーフィルタ用着色組成物およびカラーフィルタ |
| JP2004307854A (ja) * | 2003-03-27 | 2004-11-04 | Toyo Ink Mfg Co Ltd | 着色組成物及びカラーフィルタ |
| JP2005179489A (ja) * | 2003-12-19 | 2005-07-07 | Toyo Ink Mfg Co Ltd | 顔料分散剤、及びそれを含有する顔料組成物 |
| JP2007077340A (ja) * | 2005-09-16 | 2007-03-29 | Toray Ind Inc | 水性顔料分散液およびそれを用いたインク組成物 |
-
2005
- 2005-10-21 JP JP2005306685A patent/JP2007112919A/ja active Pending
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH09122470A (ja) * | 1995-10-28 | 1997-05-13 | Sanyo Shikiso Kk | 顔料分散剤 |
| JP2001188120A (ja) * | 2000-01-05 | 2001-07-10 | Toray Ind Inc | カラーフィルター用着色組成物、およびそれを使用したカラーフィルター、液晶表示装置 |
| JP2004163487A (ja) * | 2002-11-11 | 2004-06-10 | Toyo Ink Mfg Co Ltd | カラーフィルタ用着色組成物およびカラーフィルタ |
| JP2004307854A (ja) * | 2003-03-27 | 2004-11-04 | Toyo Ink Mfg Co Ltd | 着色組成物及びカラーフィルタ |
| JP2005179489A (ja) * | 2003-12-19 | 2005-07-07 | Toyo Ink Mfg Co Ltd | 顔料分散剤、及びそれを含有する顔料組成物 |
| JP2007077340A (ja) * | 2005-09-16 | 2007-03-29 | Toray Ind Inc | 水性顔料分散液およびそれを用いたインク組成物 |
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| US9580576B2 (en) | 2012-02-29 | 2017-02-28 | Canon Kabushiki Kaisha | Pigment dispersion and yellow resist composition for color filter and ink composition containing the pigment dispersion |
| JP2014002314A (ja) * | 2012-06-20 | 2014-01-09 | Sakata Corp | カラーフィルター用緑色着色組成物 |
| CN103513513A (zh) * | 2012-06-20 | 2014-01-15 | 阪田油墨股份有限公司 | 彩色滤光片用绿色着色组合物 |
| JP2017502352A (ja) * | 2013-12-23 | 2017-01-19 | エシロル アンテルナショナル（コンパーニュ ジェネラル ドプテーク） | 無色外観を有する透明光学物品 |
| JP2016065115A (ja) * | 2014-09-22 | 2016-04-28 | Jsr株式会社 | 着色組成物、着色硬化膜、並びに表示素子及び固体撮像素子 |
| CN113376963A (zh) * | 2016-09-02 | 2021-09-10 | 住友化学株式会社 | 着色组合物及化合物 |
| JP2021167412A (ja) * | 2016-09-02 | 2021-10-21 | 住友化学株式会社 | 着色組成物及び化合物 |
| CN113376962B (zh) * | 2016-09-02 | 2024-05-28 | 住友化学株式会社 | 着色组合物及化合物 |
| CN113376963B (zh) * | 2016-09-02 | 2024-05-28 | 住友化学株式会社 | 着色组合物及化合物 |
| CN113376964B (zh) * | 2016-09-02 | 2024-04-26 | 住友化学株式会社 | 着色组合物及化合物 |
| JP7315621B2 (ja) | 2016-09-02 | 2023-07-26 | 住友化学株式会社 | 着色組成物 |
| JP7217776B2 (ja) | 2016-09-02 | 2023-02-03 | 住友化学株式会社 | 着色組成物及び化合物 |
| JP2018062644A (ja) * | 2016-09-02 | 2018-04-19 | 住友化学株式会社 | 着色組成物及び化合物 |
| CN113376962A (zh) * | 2016-09-02 | 2021-09-10 | 住友化学株式会社 | 着色组合物及化合物 |
| CN113376964A (zh) * | 2016-09-02 | 2021-09-10 | 住友化学株式会社 | 着色组合物及化合物 |
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| JP2021155749A (ja) * | 2016-09-02 | 2021-10-07 | 住友化学株式会社 | 着色組成物及び化合物 |
| JP2021155746A (ja) * | 2016-09-02 | 2021-10-07 | 住友化学株式会社 | 着色組成物及び化合物 |
| JP7217777B2 (ja) | 2016-09-02 | 2023-02-03 | 住友化学株式会社 | 着色組成物及び化合物 |
| JP6991802B2 (ja) | 2016-09-02 | 2022-01-13 | 住友化学株式会社 | 着色組成物、着色硬化性組成物、カラーフィルタ、液晶表示装置、及び化合物 |
| JP7217774B2 (ja) | 2016-09-02 | 2023-02-03 | 住友化学株式会社 | 着色組成物及び化合物 |
| CN108285652A (zh) * | 2017-01-10 | 2018-07-17 | 东友精细化工有限公司 | 颜料分散组合物、着色感光性树脂组合物及其应用 |
| KR101952768B1 (ko) * | 2017-01-10 | 2019-02-27 | 동우 화인켐 주식회사 | 안료 분산 조성물, 착색 감광성 수지 조성물, 컬러필터 및 이를 포함하는 화상 표시 장치 |
| KR20180082146A (ko) * | 2017-01-10 | 2018-07-18 | 동우 화인켐 주식회사 | 안료 분산 조성물, 착색 감광성 수지 조성물, 컬러필터 및 이를 포함하는 화상 표시 장치 |
| JP7079128B2 (ja) | 2017-03-29 | 2022-06-01 | 住友化学株式会社 | 着色硬化性樹脂組成物 |
| JP2018168365A (ja) * | 2017-03-29 | 2018-11-01 | 住友化学株式会社 | 着色硬化性樹脂組成物 |
| JP6996282B2 (ja) | 2017-12-22 | 2022-01-17 | 東洋インキＳｃホールディングス株式会社 | カラーフィルタ用着色組成物、カラーフィルタ及び顔料分散剤 |
| JP2019113671A (ja) * | 2017-12-22 | 2019-07-11 | 東洋インキＳｃホールディングス株式会社 | カラーフィルタ用着色組成物、カラーフィルタ及び顔料分散剤 |
| JP2020026521A (ja) * | 2018-08-08 | 2020-02-20 | 住友化学株式会社 | 着色組成物 |
| JP7333221B2 (ja) | 2018-08-08 | 2023-08-24 | 住友化学株式会社 | 着色組成物 |
| WO2023100585A1 (ja) * | 2021-11-30 | 2023-06-08 | 富士フイルム株式会社 | 着色組成物、膜、カラーフィルタ、表示装置および構造体 |
| WO2024058001A1 (ja) * | 2022-09-16 | 2024-03-21 | 富士フイルム株式会社 | 着色組成物、膜、光学フィルタ、固体撮像素子、画像表示装置および化合物 |
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