乳液聚合
化学
透射电子显微镜
聚合
单体
聚合物
化学工程
动态光散射
水溶液
乳状液
粒子(生态学)
纳米颗粒
纳米技术
皮克林乳液
高分子化学
胶体
显微镜
胶束
纳米尺度
粒径
化学物理
电子显微镜
动力学
体积分数
作者
Megan E. Lott,Nathan D. Rosenmann,Cabell B. Eades,Jared I. Bowman,Florencia Merlino,Nathan C. Gianneschi,Brent S. Sumerlin
摘要
Heterogeneous polymerizations account for a significant fraction of global polymer production and underpin the synthesis of latexes used in coatings, adhesives, and advanced materials. Yet, despite their widespread use, emulsion polymerizations remain mechanistically underexplored due to the lack of direct observational tools compatible with liquid-phase environments. In this study, we leverage the combination of liquid-phase transmission electron microscopy (LPTEM) and dry-state transmission electron microscopy (TEM) with dynamic light scattering to visualize the nanoscale evolution of monomer droplets and particles during reversible addition-fragmentation chain-transfer (RAFT) aqueous emulsion polymerization of butyl acrylate. Using a poly(ethylene glycol)-based macro-chain transfer agent to stabilize the growing latex, we capture the progression of the emulsion mechanism, including micellar nucleation, particle growth, and relatively rare higher-order morphologies and morphological transitions in later stages. This visualization provides a mechanistic bridge between kinetic models and particle formation dynamics in emulsion systems. By addressing a key observational barrier, this work establishes a new platform for mechanistically guided design of advanced colloidal materials in solution-phase polymerization systems.
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