CN108342049B - 一种物理分相动态聚合物及其应用 - Google Patents
一种物理分相动态聚合物及其应用 Download PDFInfo
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- CN108342049B CN108342049B CN201710055920.7A CN201710055920A CN108342049B CN 108342049 B CN108342049 B CN 108342049B CN 201710055920 A CN201710055920 A CN 201710055920A CN 108342049 B CN108342049 B CN 108342049B
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- BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
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- 230000008016 vaporization Effects 0.000 description 1
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- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
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- 238000003466 welding Methods 0.000 description 1
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- 239000000811 xylitol Substances 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
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- 239000004246 zinc acetate Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- PZRXQXJGIQEYOG-UHFFFAOYSA-N zinc;oxido(oxo)borane Chemical compound [Zn+2].[O-]B=O.[O-]B=O PZRXQXJGIQEYOG-UHFFFAOYSA-N 0.000 description 1
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WO2020006721A1 (zh) * | 2018-07-04 | 2020-01-09 | 南通纺织丝绸产业技术研究院 | 一种高接枝密度环梳状聚合物及其制备方法 |
JP7202136B2 (ja) * | 2018-10-16 | 2023-01-11 | 旭化成株式会社 | N-アルキル置換アミノピリジン・フタル酸塩及びそれを含むエポキシ樹脂組成物 |
CN109498255B (zh) * | 2018-12-18 | 2020-10-09 | 温州医科大学附属第二医院、温州医科大学附属育英儿童医院 | 一种高效传热型退热贴 |
JP7229028B2 (ja) * | 2019-01-30 | 2023-02-27 | 日産化学株式会社 | N-モノ(炭化水素)イソシアヌル酸の製造方法 |
CN109821572B (zh) * | 2019-02-14 | 2022-08-19 | 上海释颉化工技术合伙企业(有限合伙) | 多孔微球聚合物负载金属型催化剂及其制备方法和应用 |
CN110562954B (zh) * | 2019-08-02 | 2022-09-30 | 安徽师范大学 | 一种荧光碳点探针的制备方法及在检测Fe2+的应用 |
CN110819115B (zh) * | 2019-11-25 | 2021-10-22 | 中国工程物理研究院总体工程研究所 | 一种具有高效自修复特性的聚硅氧烷及其制备方法 |
CN111804279A (zh) * | 2020-08-19 | 2020-10-23 | 湖南三五二环保科技有限公司 | 一种染料废水用的碳材料的制备方法及其产品和应用 |
CN114989506B (zh) * | 2022-05-17 | 2023-08-08 | 久耀电子科技(江苏)有限公司 | 阻燃低介电cof/碳氢树脂复合材料的制备方法 |
CN116023672B (zh) * | 2022-12-15 | 2024-02-06 | 江阴市星宇化工有限公司 | 一种聚合专用磷酸三钙的复合填料及其制备方法 |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1587300A (zh) * | 2004-07-15 | 2005-03-02 | 复旦大学 | 改性软硬多嵌段共轭聚合物及其制备方法 |
CN102775740A (zh) * | 2012-07-24 | 2012-11-14 | 金发科技股份有限公司 | 一种无卤阻燃弹性体组合物 |
CN104758939A (zh) * | 2015-02-26 | 2015-07-08 | 宁波大学 | 一种pH葡萄糖双敏感水凝胶的制备及应用 |
CN105646872A (zh) * | 2016-02-26 | 2016-06-08 | 翁秋梅 | 一种动态聚合物材料 |
CN105924685A (zh) * | 2016-05-03 | 2016-09-07 | 南京邮电大学 | 一种双组份高强度水凝胶及其制备方法 |
WO2016089968A3 (en) * | 2014-12-02 | 2016-11-03 | Massachusetts Institute Of Technology | Thermoreversible hydrogels from the arrested phase separation of elastin-like polypeptides |
CN106146729A (zh) * | 2016-07-04 | 2016-11-23 | 江南大学 | 一种自修复柔性印刷电路板及其制备方法 |
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Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1587300A (zh) * | 2004-07-15 | 2005-03-02 | 复旦大学 | 改性软硬多嵌段共轭聚合物及其制备方法 |
CN102775740A (zh) * | 2012-07-24 | 2012-11-14 | 金发科技股份有限公司 | 一种无卤阻燃弹性体组合物 |
WO2016089968A3 (en) * | 2014-12-02 | 2016-11-03 | Massachusetts Institute Of Technology | Thermoreversible hydrogels from the arrested phase separation of elastin-like polypeptides |
CN104758939A (zh) * | 2015-02-26 | 2015-07-08 | 宁波大学 | 一种pH葡萄糖双敏感水凝胶的制备及应用 |
CN105646872A (zh) * | 2016-02-26 | 2016-06-08 | 翁秋梅 | 一种动态聚合物材料 |
CN105924685A (zh) * | 2016-05-03 | 2016-09-07 | 南京邮电大学 | 一种双组份高强度水凝胶及其制备方法 |
CN106146729A (zh) * | 2016-07-04 | 2016-11-23 | 江南大学 | 一种自修复柔性印刷电路板及其制备方法 |
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