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A mechanistic investigation of Pickering emulsion polymerization

机译:Pickering乳液聚合的机理研究

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摘要

Pickering emulsion polymerization offers a versatile way of synthetising hybrid core–shell latexes where a polymer core is surrounded by an armour of inorganic nanoparticles. A mechanistic understanding of the polymerization process is limited which restricts the use of the technique in the fabrication of more complex, multilayered colloids. In this paper clarity is provided through an in-depth investigation into the Pickering emulsion polymerization of methyl methacrylate (MMA) in the presence of nano-sized colloidal silica (Ludox TM-40). Mechanistic insights are discussed by studying both the adsorption of the stabiliser to the surface of the latex particles and polymerization kinetics. The adhesion of the Pickering nanoparticles was found not to be spontaneous, as confirmed by cryo-TEM analysis of MMA droplets in water and monomer-swollen PMMA latexes. This supports the theory that the inorganic particles are driven towards the interface as a result of a heterocoagulation event in the water phase with a growing oligoradical. The emulsion polymerizations were monitored by reaction calorimetry in order to establish accurate values for monomer conversion and the overall rate of polymerizations (Rp). Rp increased for higher initial silica concentrations and the polymerizations were found to follow pseudo-bulk kinetics.\ud\ud
机译:Pickering乳液聚合提供了一种合成杂种核-壳胶乳的通用方法,其中聚合物核被无机纳米粒子的铠装所包围。对聚合过程的机械理解是有限的,这限制了该技术在制造更复杂的多层胶体中的使用。在本文中,通过在纳米胶体二氧化硅(Ludox TM-40)存在下对甲基丙烯酸甲酯(MMA)的Pickering乳液聚合的深入研究,提供了清晰的信息。通过研究稳定剂在胶乳颗粒表面的吸附和聚合动力学,讨论了机械的见解。如对水和单体溶胀的PMMA乳胶中的MMA液滴的冷冻TEM分析所证实的,发现Pickering纳米颗粒的粘附不是自发的。这支持了这样的理论,即由于水相中杂化现象的发生以及低聚自由基的增长,无机颗粒被驱向界面。通过反应量热法监测乳液聚合,以建立单体转化率和总聚合速率(Rp)的准确值。 Rp随较高的初始二氧化硅浓度而增加,并且发现聚合遵循拟本体动力学。\ ud \ ud

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