CN112135888A - 固化性组合物、固化性组合物套组、蓄热材料及物品 - Google Patents
固化性组合物、固化性组合物套组、蓄热材料及物品 Download PDFInfo
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- CN112135888A CN112135888A CN201880093217.8A CN201880093217A CN112135888A CN 112135888 A CN112135888 A CN 112135888A CN 201880093217 A CN201880093217 A CN 201880093217A CN 112135888 A CN112135888 A CN 112135888A
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Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1626612A (zh) * | 2003-12-13 | 2005-06-15 | 鸿富锦精密工业(深圳)有限公司 | 散热装置及其相变导热片 |
JP2007029312A (ja) * | 2005-07-25 | 2007-02-08 | Matsushita Denko Bath & Life Kk | 浴槽 |
CN101117572A (zh) * | 2007-07-25 | 2008-02-06 | 中南大学 | 以凝胶为载体的复合相变蓄热材料及其制备方法 |
CN102576766A (zh) * | 2009-10-15 | 2012-07-11 | 日立化成工业株式会社 | 导电性粘接剂、太阳能电池及其制造方法、以及太阳能电池模块 |
CN103183922A (zh) * | 2011-12-27 | 2013-07-03 | 比亚迪股份有限公司 | 用于相变储能的载体和相变储能材料及它们的制备方法 |
CN104059615A (zh) * | 2013-03-18 | 2014-09-24 | 南京工业大学 | 二元脂肪酸/pmma定形相变材料的制备方法 |
JP2016089065A (ja) * | 2014-11-06 | 2016-05-23 | 共同技研化学株式会社 | 蓄熱粘着シート |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2000109787A (ja) | 1998-10-06 | 2000-04-18 | Hope Seiyaku Kk | パラフィン類用のゲル化剤及びゲル化方法 |
JP2004026971A (ja) * | 2002-06-25 | 2004-01-29 | Idemitsu Kosan Co Ltd | 架橋蓄熱材料 |
JP4810189B2 (ja) * | 2004-11-02 | 2011-11-09 | エスケー化研株式会社 | 蓄熱断熱体 |
JP2009029985A (ja) * | 2007-07-30 | 2009-02-12 | Achilles Corp | 蓄熱性アクリル系樹脂シート状成形体 |
JP2009079115A (ja) | 2007-09-26 | 2009-04-16 | Achilles Corp | 蓄熱性ウレタン系樹脂シート状成形体 |
JP2011132421A (ja) | 2009-12-25 | 2011-07-07 | Kansai Paint Co Ltd | 親水化処理組成物 |
JP6081796B2 (ja) | 2012-12-28 | 2017-02-15 | 東邦化学工業株式会社 | 2液硬化型ポリウレタン樹脂組成物 |
JP2017132899A (ja) * | 2016-01-27 | 2017-08-03 | Jxtgエネルギー株式会社 | 硬化性樹脂組成物、硬化物の製造方法、該硬化物を備えた物品 |
WO2017200936A1 (en) * | 2016-05-19 | 2017-11-23 | Kemet Electronics Corporation | Polyanion copolymers for use with conducting polymers in solid electrolytic capacitors |
-
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Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1626612A (zh) * | 2003-12-13 | 2005-06-15 | 鸿富锦精密工业(深圳)有限公司 | 散热装置及其相变导热片 |
JP2007029312A (ja) * | 2005-07-25 | 2007-02-08 | Matsushita Denko Bath & Life Kk | 浴槽 |
CN101117572A (zh) * | 2007-07-25 | 2008-02-06 | 中南大学 | 以凝胶为载体的复合相变蓄热材料及其制备方法 |
CN102576766A (zh) * | 2009-10-15 | 2012-07-11 | 日立化成工业株式会社 | 导电性粘接剂、太阳能电池及其制造方法、以及太阳能电池模块 |
CN103183922A (zh) * | 2011-12-27 | 2013-07-03 | 比亚迪股份有限公司 | 用于相变储能的载体和相变储能材料及它们的制备方法 |
CN104059615A (zh) * | 2013-03-18 | 2014-09-24 | 南京工业大学 | 二元脂肪酸/pmma定形相变材料的制备方法 |
JP2016089065A (ja) * | 2014-11-06 | 2016-05-23 | 共同技研化学株式会社 | 蓄熱粘着シート |
Non-Patent Citations (2)
Title |
---|
宋启煌等: "《精细化工工艺学》", 30 June 1995, 化学工业出版社 * |
徐修成等: "《家庭实用胶粘剂及胶接技术》", 30 September 1995, 航空工业出版社 * |
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