微乳液
单体
自由基聚合
聚合
乳液聚合
乳状液
钴介导的自由基聚合
水溶液
机制(生物学)
高分子化学
光化学
一氧化氮介导的自由基聚合
材料科学
化学
激进的
航程(航空)
反应机理
化学工程
本体聚合
水介质
可逆加成-断裂链转移聚合
链式转移
活性自由基聚合
聚合物
作者
Juan F. Hincapié,Dorleta Otaegui,Zhong Zeng,Bernd Reck,Nicholas Ballard,José M. Asua
标识
DOI:10.1021/acsmacrolett.6c00015
摘要
Understanding the mechanism of radical entry has been a major challenge in the development of process-by-design in emulsion polymerization systems. Although many theories have been put forward across decades of experimental work, conclusive evidence of the determining factors in radical entry across the range of systems that are of industrial importance has not been forthcoming. In this work, a new technique for elucidating the root causes of radical entry is described. The technique involves the initial synthesis of a miniemulsion system in which the monomer droplets contain a hydrophobic, UV-active radical trap. This method allows the rate of entry to be followed by UV-vis spectroscopy and, furthermore, by MALDI-ToF-MS analysis of the oligomeric products present in the aqueous and organic phases; it is shown that it is possible to gain additional insights into the nature of radical entry.
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