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首页> 外文期刊>Macromolecular theory and simulations >The kinetics of free radical polymerizing systems at low conversion, 1. On the rate determining step of the bimolecular termination reaction
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The kinetics of free radical polymerizing systems at low conversion, 1. On the rate determining step of the bimolecular termination reaction

机译:自由基聚合体系在低转化率下的动力学,1.在双分子终止反应的速率确定步骤上

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Using a styrene bulk system as a model, this paper examines rates of termination at very low conversions in bulk and solution polymerizations. No definitive answer to the question of what determines such rates of termination is arrived at. Indeed, it is argued that on the basis of existing kinetic information, no such definitive answer is possible. However several things may be said with conviction. To begin with, it is rigorously shown that low conversion rates of termination cannot be explained by assuming that all radical chain end encounters result in termination, and then using center-of-mass diffusion coefficients of polymer in free solution to calculate rates of chain end encounter. However this does not mean that rates of center-of-mass diffusion do not determine rates of low conversion termination, as is shown; the idea that it may be the case that not all chain end encounters result in termination, this a manifestation of a spin multiplicity effect, is especially worthy of mention. It is also possible to explain low conversion rates of termination, as has traditionally been done, in terms of chain end motions being hindered by the presence of another polymer chain. However in concentrating on interactions between overlapping long chain macroradical coils, this traditional picture is certainly inaccurate, for it is shown that most termination interactions must involve at least one radical of shorter than expected degree of polymerization. This has the important consequence that an understanding of overall rates of dilute solution termination must be founded on an understanding of the diffusional behavior of the ends of short and intermediate length polymer chains.
机译:本文使用苯乙烯本体系统作为模型,研究了本体和溶液聚合中非常低的转化率下的终止速率。对于决定这种终止率的因素没有最终的答案。确实,有人认为,根据现有的动力学信息,不可能有这样的明确答案。但是,可以坚定地说几件事。首先,它严格地表明,不能通过假设所有自由基链端均会导致终止,然后使用游离溶液中聚合物的质心扩散系数来计算链端的速率来解释低的终止转化率遭遇。但是,这并不意味着质心扩散速率不会决定低转换终止的速率,如图所示。特别值得一提的是,并不是所有的链末端都会遇到终止的情况,这是自旋多重效应的体现。正如传统上所做的那样,还可以解释由于存在另一条聚合物链而阻碍链末端运动的低端基转化率。然而,在集中于重叠的长链大自由基线圈之间的相互作用时,该传统图像肯定是不准确的,因为已表明大多数终止相互作用必须涉及至少一个比预期的聚合度短的自由基。这具有重要的结果,即必须基于对短和中等长度聚合物链末端的扩散行为的理解来建立对稀溶液终止速率的总体理解。

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