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首页> 外文期刊>Macromolecular chemistry and physics >N-tert-butyl-1-diethylphosphono-2,2-dimethylpropyl nitroxide as counter radical in the controlled free radical polymerization of styrene: kinetic aspects
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N-tert-butyl-1-diethylphosphono-2,2-dimethylpropyl nitroxide as counter radical in the controlled free radical polymerization of styrene: kinetic aspects

机译:N-叔丁基-1-二乙基膦酰基-2,2-二甲基丙基硝基氧作为苯乙烯受控自由基聚合中的反自由基:动力学方面

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The controlled free radical polymerization of styrene with N-tert-butyl-1-diethylphosphono-2,2-dimethylpropyl nitroxide (DEPN) as counter radical was studied. Polymerizations were performed in bulk, with a DEPN-capped polystyryl as alkoxyamine initiator, in the presence of an excess of DEPN nitroxyl free radicals. Kinetics of the polymerization were followed at 115 degrees C, 125 degrees C and 130 degrees C. The equilibrium rate constant K = k(d)/k(c) of exchange between dormant and active species was determined experimentally from the slope of Ln([styrene]0/[styrene]) versus time. The obtained Arrhenius relation was the following: K(mol . L-1) = 1.45 x 10(7) exp (-113.5 kJ . mol-(RT)-R-1/), i.e., K = 1.9 x 10(-8) mol . L-1 at 125 degrees C. This result is consistent with a much faster polymerization of styrene with DEPN than with Tempo as nitroxyl counter radical (K = 2.1 x 10(-11) mol . L-1 at 125 degrees C determined previously by Fukuda). [References: 41]
机译:研究了以N-叔丁基-1-二乙基膦酰基-2,2-二甲基丙基氮氧化物(DEPN)为抗自由基的苯乙烯的受控自由基聚合。在过量的DEPN硝氧基自由基存在下,使用DEPN封端的聚苯乙烯作为烷氧基胺引发剂进行本体聚合。在115摄氏度,125摄氏度和130摄氏度下追踪聚合动力学。休眠状态和活性状态之间交换的平衡速率常数K = k(d)/ k(c)由Ln( [苯乙烯] 0 / [苯乙烯])与时间的关系。所获得的Arrhenius关系如下:K(mol。L-1)= 1.45 x 10(7)exp(-113.5 kJ mol-(RT)-R-1 /),即K = 1.9 x 10(- 8)摩尔。 L-1在125摄氏度时的结果。这一结果与苯乙烯与DEPN的聚合反应相比,与Tempo作为硝氧基抗自由基自由基的聚合要快得多(K = 2.1 x 10(-11)mol。L-1在125摄氏度时先前由福田)。 [参考:41]

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