电镀与涂饰
電鍍與塗飾
전도여도식
ELECTROPLATING & FINISHING
2013年
8期
55-58
,共4页
吴文心%陈姚%李嘉欣%赖思桃%黄湘华%蔡晓敏%张莹娇
吳文心%陳姚%李嘉訢%賴思桃%黃湘華%蔡曉敏%張瑩嬌
오문심%진요%리가흔%뢰사도%황상화%채효민%장형교
复合材料%丙烯酸酯聚氨酯%有机硅%硅溶胶%改性%乳液聚合
複閤材料%丙烯痠酯聚氨酯%有機硅%硅溶膠%改性%乳液聚閤
복합재료%병희산지취안지%유궤규%규용효%개성%유액취합
composite material%acrylate polyurethane%organic silicon%silica sol%modification%emulsion polymerization
以有机硅KH570为偶联剂,把硅溶胶引入到丙烯酸酯聚氨酯(PUA)中,采用原位分散聚合法制备了硅溶胶/有机硅改性丙烯酸酯聚氨酯(SPUA)复合材料,研究了 KH570和硅溶胶的添加量以及硅溶胶与有机硅/丙烯酸酯聚氨酯的反应时间对SPUA 复合材料平均粒径、附着力、硬度、耐水性和耐醇性的影响,获得了较佳的反应条件:KH5707.0%,硅溶胶5.5%,反应时间3 h。通过红外光谱对较佳条件下制备的SPUA复合材料进行了表征,并与市售产品进行了综合性能对比研究。结果表明,SPUA复合材料出现了N─H弯曲振动吸收峰2046 cm?1,游离态N─H键的产生说明PUA的N─H键在有机硅的作用下产生电子偏移;硅溶胶的 Si─O─H伸缩振动吸收峰从原来的3568 cm?1处移到了复合后的3442 cm?1处,且峰变宽,吸收强度变大,说明硅溶胶通过与有机硅作用接枝到PUA分子上。与市售产品比较,SPUA 复合材料的硬度、附着力、耐水性和耐醇性等性能更好。
以有機硅KH570為偶聯劑,把硅溶膠引入到丙烯痠酯聚氨酯(PUA)中,採用原位分散聚閤法製備瞭硅溶膠/有機硅改性丙烯痠酯聚氨酯(SPUA)複閤材料,研究瞭 KH570和硅溶膠的添加量以及硅溶膠與有機硅/丙烯痠酯聚氨酯的反應時間對SPUA 複閤材料平均粒徑、附著力、硬度、耐水性和耐醇性的影響,穫得瞭較佳的反應條件:KH5707.0%,硅溶膠5.5%,反應時間3 h。通過紅外光譜對較佳條件下製備的SPUA複閤材料進行瞭錶徵,併與市售產品進行瞭綜閤性能對比研究。結果錶明,SPUA複閤材料齣現瞭N─H彎麯振動吸收峰2046 cm?1,遊離態N─H鍵的產生說明PUA的N─H鍵在有機硅的作用下產生電子偏移;硅溶膠的 Si─O─H伸縮振動吸收峰從原來的3568 cm?1處移到瞭複閤後的3442 cm?1處,且峰變寬,吸收彊度變大,說明硅溶膠通過與有機硅作用接枝到PUA分子上。與市售產品比較,SPUA 複閤材料的硬度、附著力、耐水性和耐醇性等性能更好。
이유궤규KH570위우련제,파규용효인입도병희산지취안지(PUA)중,채용원위분산취합법제비료규용효/유궤규개성병희산지취안지(SPUA)복합재료,연구료 KH570화규용효적첨가량이급규용효여유궤규/병희산지취안지적반응시간대SPUA 복합재료평균립경、부착력、경도、내수성화내순성적영향,획득료교가적반응조건:KH5707.0%,규용효5.5%,반응시간3 h。통과홍외광보대교가조건하제비적SPUA복합재료진행료표정,병여시수산품진행료종합성능대비연구。결과표명,SPUA복합재료출현료N─H만곡진동흡수봉2046 cm?1,유리태N─H건적산생설명PUA적N─H건재유궤규적작용하산생전자편이;규용효적 Si─O─H신축진동흡수봉종원래적3568 cm?1처이도료복합후적3442 cm?1처,차봉변관,흡수강도변대,설명규용효통과여유궤규작용접지도PUA분자상。여시수산품비교,SPUA 복합재료적경도、부착력、내수성화내순성등성능경호。
A composite material of silica sol/acrylate polyurethane modified by organic silicon (SPUA) was prepared by in-situ dispersion polymerization with organic silicon KH570 as coupling agent and silica sol incorporated into acrylate polyurethane (PUA). The effects of the amounts of KH570 and silica sol as well as the reaction time of silica sol with organic/acrylate polyurethane on average particle size, adhesion, hardness, water resistance, and alcohol resistance of the SPUA composite material were studied. The optimal reaction conditions were obtained as follows:KH570 7.0%, silica sol 5.5%, and reaction time 3 h. The SPUA composite material prepared under the above conditions was characterized by infrared spectroscopy, and its comprehensive performances were compared with that of commercial product. The results showed that a N─H bending vibration absorption peak appears at 2 046 cm?1 for SPUA composite material, and the formation of free N─H bond indicates that the N─H bond of PUA produces electron shifting as a results of the action of organic silicon. A wider Si─O─H flexing vibration absorption peak of silica sol shifts from 3 568 cm?1 to 3 442 cm?1 and becomes wider and stronger after composition, showing that silica sol is grafted to PUA molecule through its action with organic silicon. The hardness, adhesion, water resistance, and alcohol resistance of the SPUA composite material are better in comparison with that of the commercial product.