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One-pot formation of monodisperse polymer@SiO2 core-shell nanoparticles via surfactant-free emulsion polymerization using an adaptive silica precursor polymerстатья
Статья опубликована в высокорейтинговом журнале
Информация о цитировании статьи получена из
Web of Science,
Scopus
Статья опубликована в журнале из списка Web of Science и/или Scopus
Дата последнего поиска статьи во внешних источниках: 9 ноября 2017 г.
- Авторы: Zhao Yongliang, Wang Haitao, Zhu Xiaomin, Moeller Martin
- Журнал: Polymer Chemistry
- Том: 8
- Номер: 40
- Год издания: 2017
- Первая страница: 6263
- Последняя страница: 6271
- DOI: 10.1039/c7py01264k
- Аннотация: Aqueous emulsion polymerization is by far the most important method for synthesizing polymer nano-particles. In this work we report a new type of surfactant-free emulsion polymerization process for one-pot formation of monodisperse poly(methyl methacrylate)@SiO2 core-shell nanoparticles. The strategy utilizes a silica precursor polymer, hyperbranched polyethoxysiloxane (PEOS), whose chemical structure can be adapted by hydrolysis at water/oil interfaces for their stabilization. The core-shell particles are obtained simply by adding a monomer/PEOS solution into water and subsequent heating to initiate polymerization. A high-shear emulsification step that is undesirable for industrial scale-up is not needed. In contrast to most emulsion polymerization processes where water soluble initiators are employed, an oil soluble initiator is required in this process for achieving narrow particle size distribution and precise control of silica content in the particles. As the polymerization proceeds, the growing chains are precipitated from the aqueous phase forming polymer particles, which are in turn stabilized by partially hydrolysed amphiphilic PEOS molecules. After the polymerization is complete, the conversion of PEOS continues depositing silica onto the silica-coated polymer particles. This method allows an easy control of silica shell thickness by varying the PEOS concentration and the particle size can be adjusted by changing the pH of the aqueous phase.
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