材料科学
分散性
聚合
单体
聚合物
甲基丙烯酸甲酯
X射线光电子能谱
傅里叶变换红外光谱
硅烷
化学工程
沉淀聚合
动态光散射
透射电子显微镜
高分子化学
复合材料
纳米颗粒
自由基聚合
纳米技术
工程类
作者
Shengwei Guo,Xin Wang,Guxia Wang,Min Nie
标识
DOI:10.1002/slct.201900426
摘要
Abstract Ultrasonically initiated graft polymerization is employed to prepare poly (methyl methacrylate)/silicon dioxide (PMMA/SiO 2 ) core‐shell particles and PMMA microcapsules. Monodisperse SiO 2 particles are obtained by the Stöber method. Its surface is modified with γ‐methacryloxypropyl trimethoxy silane (MPS) to introduce unsaturated double bonds. And then MMA and MPS are copolymerized under ultrasonic initiation to prepare PMMA/SiO 2 core‐shell particles. PMMA microcapsules are obtained by etching SiO 2 with the HF aqueous solution. The morphology and size of the core‐shell particles and polymer microcapsules are analysed using transmission electron microscopy (TEM) and dynamic light scattering (DLS). The encapsulation state is determined using a Fourier transform infrared spectrometer (FTIR) and X‐ray photoelectron spectrometer (XPS). The results show that both the core‐shell particles and the polymer microcapsules have perfect core‐shell or hollow structures. The control of shell thickness can be easily realized by adjusting the amount of monomer, e. g. 30 nm, 50 nm and 80 nm, respectively. And in the inner of the shell, PMMA is anchored onto the surface of SiO 2 core with covalent bonds. As the monomer amount increases, the contents of Si, O, and C change accordingly. And the polymer shell would become denser and thicker.
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