Guo Yi, Zetterlund Per B
Centre for Advanced Macromolecular Design (CAMD), School of Chemical Engineering, The University of New South Wales, Sydney, NSW 2052, Australia.
ACS Macro Lett. 2012 Jun 19;1(6):748-752. doi: 10.1021/mz300213j. Epub 2012 Jun 1.
A novel approach is presented whereby nitroxide-mediated radical polymerization (NMP) is conducted in an aqueous heterogeneous system at an initial polymerization rate an order of magnitude greater than the corresponding bulk system, accompanied by an improvement in the level of control over the molecular weight distribution. NMP of styrene mediated by --butyl--[1-diethylphosphono-(2,2-dimethylpropyl)] nitroxide (SG1) at 90 °C was performed in a miniemulsion with exceptionally small particles of number-average diameter ∼10 nm, generated by ultrasonication combined with in situ surfactant formation. The results are discussed in terms of the effects of compartmentalization, nitroxide partitioning (exit/entry), and a rate-enhancing effect of oleic acid. These findings illustrate that it is possible to significantly improve the performance of an NMP process by the exploitation of intrinsic effects of heterogeneous systems.
本文提出了一种新方法,即在水相非均相体系中进行氮氧自由基介导的自由基聚合(NMP),其初始聚合速率比相应的本体体系高一个数量级,同时分子量分布的控制水平有所提高。在90℃下,由丁基-[1-二乙基膦酰基-(2,2-二甲基丙基)]氮氧自由基(SG1)介导的苯乙烯NMP在细乳液中进行,通过超声处理结合原位表面活性剂形成产生了数均直径约为10nm的异常小的颗粒。从分隔效应、氮氧自由基分配(进出)以及油酸的速率增强效应方面对结果进行了讨论。这些发现表明,通过利用非均相体系的内在效应,可以显著提高NMP过程的性能。