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Nitroxide-mediated living free radical miniemulsion polymerization of styrene

机译:一氧化氮介导的苯乙烯活性自由基微乳液聚合

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摘要

Living free-radical bulk polymerization using a stable free r; initiator system based on nitroxide stable radicals such as TEMPO (2,2 tetramethyl-l -piperidynyloxy) has permitted the synthesis of polymers molecular weight distributions only slightly broader than those obtained via ar polymerization (PDI < 1.3). Most recently we were able to successfully appl living free-radical polymerization in a miniemulsion polymerization process: prepare stable latexes with 20% solids and having relatively narrow mole weight distributions (1.14 - 1.6). Styrene miniemulsions were prepared using anionic surfactant Dowfax 8390 with hexadecane as costabilizer. The miniemu polymerizations were carried out at 125 degrees C in pressure bottles using be peroxide (BPO) and TEMPO. The kinetics of the living free radical miniemu polymerization were followed as a function of the [TEMPO]/[BPO] ratio in ore develop a mechanistic understanding of the nucleation and growth processes in disperse system. The development of particle number and the total numb polymer chains (through the molecular weight analysis) during the cour polymerizations in the presence and absence of TEMPO are used to deve comprehensive picture of the process. [References: 24]
机译:使用稳定的游离基进行活性自由基本体聚合;基于氮氧化物稳定基团的引发剂体系,例如TEMPO(2,2-四甲基-1-哌啶基氧基),允许合成的聚合物分子量分布仅比通过ar聚合获得的分子量分布稍宽(PDI <1.3)。最近,我们能够在细乳液聚合工艺中成功地进行自由基聚合:制备具有20%固体含量和相对窄的分子量分布(1.14-1.6)的稳定胶乳。使用阴离子表面活性剂Dowfax 8390和十六烷作为助稳定剂制备苯乙烯细乳液。使用e过氧化物(BPO)和TEMPO,在125℃的压力瓶中进行小e聚合。随活性自由基最小e聚合反应的动力学变化,随矿石中[TEMPO] / [BPO]比的变化,对分散体系中成核和生长过程的机理有了深入的了解。在存在和不存在TEMPO的情况下,在聚合反应过程中,颗粒数和总的聚合物链数(通过分子量分析)的发展都可用于对该过程进行全面描述。 [参考:24]

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