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RAFT-Mediated Emulsion Polymerization of Styrene using a Non-Ionic Surfactant

机译:非离子表面活性剂的RAFT介导的苯乙烯乳液聚合

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We report the successful RAFT-mediated emulsion polymerization of styrene using a non-ionic surfactant (Brij98),the highly reactive 1-phenylethyl phenyldithioacetate (PEPDTA)RAFT agent,and water-soluble initiator ammonium persulfate (APS).The molar ratio of RAFT agent to APS was identical in all experiments.Most of the monomer was contained within the micelles,analogous to microemulsion or miniemulsion systems but without the need of shear,sonication,cosurfactant,or a hydrophobe.The number-average molecular weight increased with conversion and the polydispersity index was below 1.2.This ideal 'living'behavior was only found when molecular weights of 9000 and below were targeted.It was postulated that the rapid transportation of RAFT agent from the monomer swollen micelles to the growing particles was fast on the polymerization timescale,and most if not all the RAFT agent is consumed within the first 10% conversion.In addition,it was postulated that the high nucleation rate from the high rate of exit (of the R radical from the RAFT agent)and high entry rate from water-phase radicals (high APS concentration)reduced the effects of 'superswelling'and therefore a similar molar ratio of RAFT agent to monomer was maintained in all growing particles.The high polydispersity indexes found when targeting molecular weights greater than 9000 were postulated to be due to the lower nucleation rate from the lower weight fractions of both APS and RAFT agent.In these cases,'superswelling'played a dominant role leading to a heterogeneous distribution of RAFT to monomer ratios among the particles nucleated at different times.
机译:我们报道了使用非离子表面活性剂(Brij98),高反应性1-苯基乙基苯基二硫代乙酸酯(PEPDTA)RAFT试剂和水溶性引发剂过硫酸铵(APS)成功进行RAFT介导的苯乙烯乳液聚合的方法.RAFT的摩尔比在所有实验中,APS的活性剂是相同的。大多数单体都包含在胶束中,类似于微乳液或细乳液体系,但不需要剪切,超声处理,助表面活性剂或疏水物。数均分子量随转化率和分子量的增加而增加。多分散指数低于1.2。只有在分子量达到9000及以下时才发现这种理想的``活性''行为。据推测,RAFT剂从单体溶胀的胶束到增长的颗粒的快速运输在聚合反应中是快速的。时间尺度,并且大多数(如果不是全部)RAFT剂在最初的10%转化过程中被消耗掉。此外,据推测,hig的高成核率h(RAFT试剂中R自由基的逸出速率)和水相自由基的高进入速率(高APS浓度)降低了'超溶胀'的作用,因此,在所有情况下,RAFT试剂与单体的摩尔比均保持相似假定分子量大于9000时发现高多分散指数是由于APS和RAFT剂的重量分数较低导致成核率降低。在这些情况下,``超溶胀''起着主导作用,导致在不同时间成核的颗粒中,RAFT与单体比率的不均匀分布。

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