CN109852193A - 一种水性环氧树脂及其制备方法 - Google Patents
一种水性环氧树脂及其制备方法 Download PDFInfo
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- CN109852193A CN109852193A CN201811640849.XA CN201811640849A CN109852193A CN 109852193 A CN109852193 A CN 109852193A CN 201811640849 A CN201811640849 A CN 201811640849A CN 109852193 A CN109852193 A CN 109852193A
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- epoxy resins
- aqueous epoxy
- ether
- methacrylate
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- Epoxy Resins (AREA)
- Paints Or Removers (AREA)
Abstract
Description
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111087544A (zh) * | 2019-12-23 | 2020-05-01 | 浙江中科立德新材料有限公司 | 海洋多糖类水性树脂及其制备方法 |
CN111748309A (zh) * | 2020-07-09 | 2020-10-09 | 漳州市锐普化工有限公司 | 一种耐高温高湿的环保胶黏剂及其制备方法 |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102432773A (zh) * | 2011-08-29 | 2012-05-02 | 河北科技大学 | 一种水性环氧丙烯酸酯接枝复合乳液及其制备方法 |
EP2592099A1 (de) * | 2011-11-10 | 2013-05-15 | Sika Technology AG | Aromatische Aminogruppen aufweisende Härter für Epoxidharze |
CN103467748A (zh) * | 2013-08-13 | 2013-12-25 | 嘉兴市清河高力绝缘有限公司 | 水性丙烯酸改性环氧酯乳液及其氨基烤漆的制备方法 |
CN107011770A (zh) * | 2017-05-19 | 2017-08-04 | 江苏三木化工股份有限公司 | 一种自干漆用水性环氧树脂及制备方法与应用 |
CN107629172A (zh) * | 2017-10-27 | 2018-01-26 | 浙江理工大学 | 一种常温固化单组份水性环氧树脂分散体的制备方法 |
CN108559090A (zh) * | 2018-04-26 | 2018-09-21 | 中山大桥化工集团有限公司 | 一种水性环氧改性丙烯酸树脂及其制备方法 |
-
2018
- 2018-12-29 CN CN201811640849.XA patent/CN109852193B/zh active Active
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102432773A (zh) * | 2011-08-29 | 2012-05-02 | 河北科技大学 | 一种水性环氧丙烯酸酯接枝复合乳液及其制备方法 |
EP2592099A1 (de) * | 2011-11-10 | 2013-05-15 | Sika Technology AG | Aromatische Aminogruppen aufweisende Härter für Epoxidharze |
CN103467748A (zh) * | 2013-08-13 | 2013-12-25 | 嘉兴市清河高力绝缘有限公司 | 水性丙烯酸改性环氧酯乳液及其氨基烤漆的制备方法 |
CN107011770A (zh) * | 2017-05-19 | 2017-08-04 | 江苏三木化工股份有限公司 | 一种自干漆用水性环氧树脂及制备方法与应用 |
CN107629172A (zh) * | 2017-10-27 | 2018-01-26 | 浙江理工大学 | 一种常温固化单组份水性环氧树脂分散体的制备方法 |
CN108559090A (zh) * | 2018-04-26 | 2018-09-21 | 中山大桥化工集团有限公司 | 一种水性环氧改性丙烯酸树脂及其制备方法 |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111087544A (zh) * | 2019-12-23 | 2020-05-01 | 浙江中科立德新材料有限公司 | 海洋多糖类水性树脂及其制备方法 |
CN111748309A (zh) * | 2020-07-09 | 2020-10-09 | 漳州市锐普化工有限公司 | 一种耐高温高湿的环保胶黏剂及其制备方法 |
CN111748309B (zh) * | 2020-07-09 | 2021-11-26 | 漳州市锐普化工有限公司 | 一种耐高温高湿的环保胶黏剂及其制备方法 |
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