RU2015118590A - Дисперсии полимерных частиц с дивиниларендиоксидами - Google Patents
Дисперсии полимерных частиц с дивиниларендиоксидами Download PDFInfo
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Abstract
1. Композиция, содержащая:a) от 45 до 97 мас.% дивиниларендиоксида; иb) от 3 до 55 мас.% каучука типа ядро-оболочка, включающего ядро частицы каучука и слой оболочки, где указанный каучук типа ядро-оболочка имеет размер частиц от 0,01 мкм до 0,50 мкм.2. Композиция по п. 1, где дивиниларендиоксид включает дивинилбензолдиоксид.3. Композиция по любому из предшествующих пунктов, где дивиниларендиоксид содержит примеси менее чем 50%.4. Композиция по п. 1 или 2, где каучук типа ядро-оболочка имеет ядро, выбранное из группы, состоящей из бутадиенового ядра, силиконового ядра, ядра из сополимера бутадиен-стирол и их комбинаций.5. Композиция по п. 3, где каучук типа ядро-оболочка имеет ядро, выбранное из группы, состоящей из бутадиенового ядра, силиконового ядра, ядра из сополимера бутадиен-стирол и их комбинаций.6. Композиция по любому из пп. 1, 2 или 5, где каучук типа ядро-оболочка имеет оболочку, выбранную из группы, состоящей из метилметакрилатной оболочки, стирольной оболочки и их комбинаций.7. Композиция по п. 4, где каучук типа ядро-оболочка имеет оболочку, выбранную из группы, состоящей из метилметакрилатной оболочки, стирольной оболочки и их комбинаций.8. Композиция по любому из пп. 1, 2, 5 или 7, где каучук типа ядро-оболочка дополнительно включает промежуточный слой.9. Способ получения композиции по любому из предшествующих пунктов, включающий диспергирование каучука типа ядро-оболочка в компоненте на основе дивиниларендиоксида в смесителе высокого сдвига в условиях диспергирования, включающих температуру диспергирования от 40°С до 100°С, число Рейнольдса, большее 10, и время диспергирования от 30 минут до 80 минут.10. Композиция, содержащая:a) эпоксидную смолу;b) отвердитель; иc) агент повышения ударной вязкости,
Claims (19)
1. Композиция, содержащая:
a) от 45 до 97 мас.% дивиниларендиоксида; и
b) от 3 до 55 мас.% каучука типа ядро-оболочка, включающего ядро частицы каучука и слой оболочки, где указанный каучук типа ядро-оболочка имеет размер частиц от 0,01 мкм до 0,50 мкм.
2. Композиция по п. 1, где дивиниларендиоксид включает дивинилбензолдиоксид.
3. Композиция по любому из предшествующих пунктов, где дивиниларендиоксид содержит примеси менее чем 50%.
4. Композиция по п. 1 или 2, где каучук типа ядро-оболочка имеет ядро, выбранное из группы, состоящей из бутадиенового ядра, силиконового ядра, ядра из сополимера бутадиен-стирол и их комбинаций.
5. Композиция по п. 3, где каучук типа ядро-оболочка имеет ядро, выбранное из группы, состоящей из бутадиенового ядра, силиконового ядра, ядра из сополимера бутадиен-стирол и их комбинаций.
6. Композиция по любому из пп. 1, 2 или 5, где каучук типа ядро-оболочка имеет оболочку, выбранную из группы, состоящей из метилметакрилатной оболочки, стирольной оболочки и их комбинаций.
7. Композиция по п. 4, где каучук типа ядро-оболочка имеет оболочку, выбранную из группы, состоящей из метилметакрилатной оболочки, стирольной оболочки и их комбинаций.
8. Композиция по любому из пп. 1, 2, 5 или 7, где каучук типа ядро-оболочка дополнительно включает промежуточный слой.
9. Способ получения композиции по любому из предшествующих пунктов, включающий диспергирование каучука типа ядро-оболочка в компоненте на основе дивиниларендиоксида в смесителе высокого сдвига в условиях диспергирования, включающих температуру диспергирования от 40°С до 100°С, число Рейнольдса, большее 10, и время диспергирования от 30 минут до 80 минут.
10. Композиция, содержащая:
a) эпоксидную смолу;
b) отвердитель; и
c) агент повышения ударной вязкости, включающий
i) от 45 до 97 мас.% дивиниларендиоксида; и
ii) от 3 до 55 мас.% каучука типа ядро-оболочка, включающего ядро частицы каучука и слой оболочки, где каучук типа ядро-оболочка имеет размер частиц от 0,01 мкм до 0,03 мкм.
11. Композиция по п. 10, где отвердитель выбран из группы, состоящей из алифатических аминов, циклоалифатических аминов, ароматических аминов, ангидридов, амидоаминов, полиамида, дициклоамида и сложных цианатных эфиров.
12. Композиция по любому из пп. 10 или 11, где каучук типа ядро-оболочка дополнительно включает промежуточный слой.
13. Композиция по любому из пп. 10 или 11, где дивиниларендиоксид включает дивинилбензолдиоксид.
14. Композиция по п. 12, где дивиниларендиоксид включает дивинилбензолдиоксид.
15. Композиция по любому из пп. 10 или 11, где дивиниларендиоксид содержит примесей менее чем 50%.
16. Композиция по п. 14, где дивиниларендиоксид содержит примесей менее чем 50%.
17. Композиционный материал, полученный из композиции по п. 1.
18. Покрытие, полученное из композиции по п. 1.
19. Клей, полученный из композиции по п. 1.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201261715925P | 2012-10-19 | 2012-10-19 | |
US61/715,925 | 2012-10-19 | ||
PCT/US2013/065385 WO2014062891A1 (en) | 2012-10-19 | 2013-10-17 | Polymer particle dispersions with divinylarene dioxides |
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RU2015118590A true RU2015118590A (ru) | 2016-12-10 |
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RU2015118590A RU2015118590A (ru) | 2012-10-19 | 2013-10-17 | Дисперсии полимерных частиц с дивиниларендиоксидами |
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US (1) | US20150247031A1 (ru) |
EP (1) | EP2909268A1 (ru) |
JP (1) | JP2016500728A (ru) |
CN (1) | CN104704047A (ru) |
BR (1) | BR112015008196A2 (ru) |
RU (1) | RU2015118590A (ru) |
TW (1) | TW201418353A (ru) |
WO (1) | WO2014062891A1 (ru) |
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US9617413B2 (en) * | 2012-10-01 | 2017-04-11 | Dow Global Technologies Llc | Curable epoxy resin compositions |
JP7217258B2 (ja) * | 2017-07-12 | 2023-02-02 | ヘクセル コンポジッツ、リミテッド | 樹脂組成物 |
CN116102712B (zh) * | 2022-12-28 | 2024-06-25 | 厦门大学 | 一种环氧树脂增韧剂及其制备方法和应用 |
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Publication number | Priority date | Publication date | Assignee | Title |
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US2750395A (en) | 1954-01-05 | 1956-06-12 | Union Carbide & Carbon Corp | Diepoxides |
US2890194A (en) | 1956-05-24 | 1959-06-09 | Union Carbide Corp | Compositions of epoxides and polycarboxylic acid compounds |
US3018262A (en) | 1957-05-01 | 1962-01-23 | Shell Oil Co | Curing polyepoxides with certain metal salts of inorganic acids |
US2924580A (en) | 1957-08-08 | 1960-02-09 | Union Carbide Corp | Divinyl benzene dioxide compositions |
EP0776917B1 (de) * | 1995-11-29 | 2002-05-29 | Vantico AG | Core/Shell-Partikel und diese enthaltende härtbare Epoxidharzzusammensetzungen |
JP5027509B2 (ja) * | 2004-08-18 | 2012-09-19 | 株式会社カネカ | 半導体封止剤用エポキシ樹脂組成物およびエポキシ樹脂成形材料 |
US20080287586A1 (en) * | 2007-03-22 | 2008-11-20 | Jones Jamie N | Functionalized nanoparticles and their use in particle/bulk material systems |
BRPI0918349A2 (pt) | 2008-12-30 | 2015-08-11 | Dow Global Technologies Llc | Processo para preparar dióxido de divinilareno |
WO2011015716A1 (fr) * | 2009-08-04 | 2011-02-10 | Arkema France | Particules de type " cœur-ecorce " comprenant une ecorce a base de monomeres hydrophiles |
WO2011063327A2 (en) * | 2009-11-23 | 2011-05-26 | Dow Global Technologies Llc. | Toughened epoxy resin formulations |
CA2803851A1 (en) * | 2010-06-25 | 2011-12-29 | Dow Global Technologies Llc | Curable epoxy resin compositions and composites made therefrom |
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2013
- 2013-10-17 WO PCT/US2013/065385 patent/WO2014062891A1/en active Application Filing
- 2013-10-17 US US14/432,770 patent/US20150247031A1/en not_active Abandoned
- 2013-10-17 EP EP13786048.2A patent/EP2909268A1/en not_active Withdrawn
- 2013-10-17 RU RU2015118590A patent/RU2015118590A/ru unknown
- 2013-10-17 CN CN201380052926.9A patent/CN104704047A/zh active Pending
- 2013-10-17 JP JP2015537815A patent/JP2016500728A/ja active Pending
- 2013-10-17 BR BR112015008196A patent/BR112015008196A2/pt not_active IP Right Cessation
- 2013-10-18 TW TW102137741A patent/TW201418353A/zh unknown
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WO2014062891A1 (en) | 2014-04-24 |
JP2016500728A (ja) | 2016-01-14 |
BR112015008196A2 (pt) | 2017-07-04 |
EP2909268A1 (en) | 2015-08-26 |
CN104704047A (zh) | 2015-06-10 |
TW201418353A (zh) | 2014-05-16 |
US20150247031A1 (en) | 2015-09-03 |
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