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首页> 外文期刊>Polymer Degradation and Stability >Physico-chemical aspects of polyethylene processing in an open mixer. Part 16: Mechanisms and kinetics of ketone formation at low temperature
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Physico-chemical aspects of polyethylene processing in an open mixer. Part 16: Mechanisms and kinetics of ketone formation at low temperature

机译:在开放式混合机中聚乙烯加工的物理化学方面。第16部分:低温下酮形成的机理和动力学

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Ketones are formed essentially on various reactions of polyethylene hydroperoxide. In the low temperature range (150—160℃), some reactions are the same as in the high temperature range (170—200℃) of the experiments. However, there is much more complexity at low temperature than at high temperature. The experimental kinetics reveals three significantly different processes compared to only two at high temperature. Ketone formation according to a constant rate results from the cage reaction between a peroxy radical and a hydroperoxide group during the chain propagation reaction. One of the reactions envisaged for the ketones formed according to the rate increasing with processing time in the initial stages is similar from the chemical point of view to the reaction yielding ketones according to the constant rate. The reaction proceeds between the hydroperoxides accumulated in an elementary volume and the peroxy radicals responsible for an additional oxidation of this volume. It cannot be accounted for by formal homogeneous kinetics that accounts well for the constant rate but by the heterogeneous kinetics taking into account repeated oxidation of elementary volumes. The second possibility of ketone formation according to the rate increasing with time is based on bimolecular hydroperoxide decomposition involving mainly associated hydroperoxides. The kinetic treatment for this process combines the heterogeneous kinetics of oxidation volume overlapping with monomolecular decomposition of associated hydroperoxides. The rate constant deduced from the data is in agreement with literature values as well as with the values deduced previously from the experiments with PE melts.
机译:基本上在聚乙烯氢过氧化物的各种反应上形成酮。在低温(150-160℃)下,某些反应与实验的高温(170-200℃)相同。但是,低温下的复杂性要比高温下大得多。实验动力学揭示了三个明显不同的过程,而高温下只有两个。在链增长反应期间,过氧自由基与氢过氧化物基团之间的笼式反应导致了以恒定速率形成酮。从化学观点来看,在初始阶段根据速率随处理时间增加而形成的酮设想的反应之一类似于根据恒定速率生成酮的反应。反应在基本体积中积累的氢过氧化物与负责该体积的进一步氧化的过氧自由基之间进行。它不能通过形式上均一的动力学来解释,该形式的匀速动力学很好地说明了恒定速率,而不能通过考虑元素体积重复氧化的异质动力学来解释。根据速率随时间增加而形成酮的第二种可能性是基于双分子氢过氧化物分解,其中主要涉及缔合的氢过氧化物。此过程的动力学处理将氧化体积的异质动力学与相关氢过氧化物的单分子分解相结合。从数据推导的速率常数与文献值以及先前从PE熔体的实验推导的值一致。

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