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通过水乳液聚合制备的全丙烯酸酯成膜胶体聚合物/二氧化硅纳米复合材料颗粒。

All-acrylic film-forming colloidal polymer/silica nanocomposite particles prepared by aqueous emulsion polymerization.

机构信息

Dainton Building, Department of Chemistry, The University of Sheffield, Brook Hill, Sheffield, S3 7HF, UK.

出版信息

Langmuir. 2011 Sep 6;27(17):11129-44. doi: 10.1021/la202066n. Epub 2011 Aug 1.

DOI:10.1021/la202066n
PMID:21776995
Abstract

The efficient synthesis of all-acrylic, film-forming, core-shell colloidal nanocomposite particles via in situ aqueous emulsion copolymerization of methyl methacrylate with n-butyl acrylate in the presence of a glycerol-functionalized ultrafine silica sol using a cationic azo initiator at 60 °C is reported. It is shown that relatively monodisperse nanocomposite particles can be produced with typical mean weight-average diameters of 140-330 nm and silica contents of up to 39 wt %. The importance of surface functionalization of the silica sol is highlighted, and it is demonstrated that systematic variation of parameters such as the initial silica sol concentration and initiator concentration affect both the mean particle diameter and the silica aggregation efficiency. The nanocomposite morphology comprises a copolymer core and a particulate silica shell, as determined by aqueous electrophoresis, X-ray photoelectron spectroscopy, and electron microscopy. Moreover, it is shown that films cast from n-butyl acrylate-rich copolymer/silica nanocomposite dispersions are significantly more transparent than those prepared from the poly(styrene-co-n-butyl acrylate)/silica nanocomposite particles reported previously. In the case of the aqueous emulsion homopolymerization of methyl methacrylate in the presence of ultrafine silica, a particle formation mechanism is proposed to account for the various experimental observations made when periodically sampling such nanocomposite syntheses at intermediate comonomer conversions.

摘要

通过在 60°C 下使用阳离子偶氮引发剂,在甘油功能化的超细二氧化硅溶胶存在下,将甲基丙烯酸甲酯与正丁酯原位进行水乳液共聚,高效合成了全丙烯酸、成膜、核壳胶体纳米复合材料颗粒。结果表明,相对单分散的纳米复合材料颗粒可以用典型的重均直径为 140-330nm 和二氧化硅含量高达 39wt%来生产。强调了二氧化硅溶胶表面功能化的重要性,并表明初始二氧化硅溶胶浓度和引发剂浓度等参数的系统变化会影响平均粒径和二氧化硅聚集效率。通过水电泳、X 射线光电子能谱和电子显微镜确定了纳米复合材料的形态由共聚物核和颗粒状二氧化硅壳组成。此外,还表明由富含正丁酯的共聚物/二氧化硅纳米复合材料分散体浇铸的薄膜比以前报道的由聚苯乙烯-共-正丁酯/二氧化硅纳米复合材料颗粒制备的薄膜具有更高的透明度。在超细二氧化硅存在下进行甲基丙烯酸甲酯的水乳液均聚的情况下,提出了一种颗粒形成机制,以解释在这种纳米复合材料合成的中间共聚单体转化率下周期性取样时所观察到的各种实验结果。

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