首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >Effects of the oil-water interface on network formation in nanogel synthesis using nitroxide-mediated radical copolymerization of styrene/divinylbenzene in miniemulsion
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Effects of the oil-water interface on network formation in nanogel synthesis using nitroxide-mediated radical copolymerization of styrene/divinylbenzene in miniemulsion

机译:油水界面对细乳液中氮氧化物介导的苯乙烯/二乙烯基苯自由基共聚合的纳米凝胶合成中网络形成的影响

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摘要

Nitroxide-mediated radical copolymerization of styrene (99 mol%)/divinylbenzene (1 mol%) employing the nitroxide 2,2,6,6-tetramethylpiperidinyl-1-oxy (TEMPO) in aqueous miniemulsion using sodium dodecylbenzenesulfonate as surfactant has been carried out at 125 degrees C. At a given styrene conversion, the degree of crosslinking increases with decreasing polystyrene-TEMPO macroinitiator concentration in excess of what is predicted based on the increase in primary chain length assuming an ideal controlled/living process. This discrepancy is mainly a result of the oil-water interface effect on the deactivation reaction between propagating radicals and TEMPO. This interface effect causes a marked increase in primary chain length, and therefore an accompanying increase in the number of crosslinks per primary chain. Polymerizations in the presence of free TEMPO minimizes the interface effect, and one then obtains molecular weight distributions and well-defined networks conducive with a control led/living process.
机译:使用十二烷基苯磺酸钠作为表面活性剂,在水性细乳液中使用硝基氧化2,2,6,6-四甲基哌啶基-1-氧基(TEMPO),进行了硝基苯乙烯介导的苯乙烯(99 mol%)/二乙烯基苯(1 mol%)的自由基共聚合。在125℃下。在给定的苯乙烯转化率下,交联度随着聚苯乙烯-TEMPO大分子引发剂浓度的降低而增加,其超过基于理想的控制/活性过程的基于主链长度的增加所预测的。这种差异主要是由于油水界面作用对自由基和TEMPO之间的钝化反应的影响。这种界面效应导致主链长度显着增加,因此伴随着每条主链交联数的增加。在游离TEMPO的存在下进行聚合可最大程度地降低界面效应,然后获得分子量分布和明确定义的网络,这有利于控制引发/活化过程。

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