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作 者:洪友良[1] 商铁存[1] 靳玉伟[1] 杨帆[1] 王策[1]
机构地区:[1]吉林大学麦克德尔米德实验室,长春130012
出 处:《高等学校化学学报》2005年第5期985-987,F013,共4页Chemical Journal of Chinese Universities
基 金:国家自然科学基金(批准号:50173009);国家"九七三"计划项目(批准号:2001CB610500);国家自然科学基金重大国际合作项目(批准号:20320120169)资助.
摘 要:The preparation and formation mechanism of silica/polyvinylpyrrolidone(PVP)-polyacrylonitrile(PAN) coaxial nanofibers were presented in this paper. The PVP-PAN composite nanofibers were obtained via an electrospinning technique, while SiO2 nanoparticles were prepared according to a Stber method. The measurements of water contact angle(WCA), the compared results of silica coating PVP-PAN composite nanofibers with PAN nanofibers indicate that much PVP resided on the composite nanofiber surface, which results in the occurrence of SiO2@polymer coaxial nanofibers due to the formation of hydrogen bonding between silica and composite nanofibers and subsequent adsorption of silica on the fiber surface.The preparation and formation mechanism of silica/polyvinylpyrrolidone(PVP)-polyacrylonitrile(PAN) coaxial nanofibers were presented in this paper. The PVP-PAN composite nanofibers were obtained via an electrospinning technique, while SiO_2 nanoparticles were prepared according to a Stber method. The measurements of water contact angle(WCA), the compared results of silica coating PVP-PAN composite nanofibers with PAN nanofibers indicate that much PVP resided on the composite nanofiber surface, which results in the occurrence of SiO_2@polymer coaxial nanofibers due to the formation of hydrogen bonding between silica and composite nanofibers and subsequent adsorption of silica on the fiber surface.
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