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Polymerization-induced phase separation: Intermediate dynamics

机译:聚合诱导的相分离:中间动力学

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摘要

When phase separation is induced by polymerizating monomers in a mixture of monomers and nonreacting molecules, the dynamics is different depending on the time scale of polymerization tau(pl) and the time scale of phase separation tau(ps) Previous studies have explored the dynamic regimes where tau(pl) tau(ps) and that where tau(pl) tau(ps). In the former, a spanning gel emerges before the phase separation and the phase separation is driven largely by activation. In the latter, phase separation occurs first between polymers and nonbonding molecules and then the polymers turn into a gel, and therefore the driving mechanism is the same as in the usual liquid-liquid demixing processes. Using Molecular Dynamics simulations, we explore in this paper the intermediate dynamic regime where the two time scales are comparable. When the polymerization is done by means of the thermal condensation reaction, we observe the expected crossover, one limit behavior at early times and then the other at late times. When the polymerization is done by means of the radical addition reaction, the results suggest that the driving mechanism changes more than once. [References: 10]
机译:当通过在单体和非反应分子的混合物中聚合单体来诱导相分离时,动力学取决于聚合tau(pl)的时间尺度和相分离tau(ps)的时间尺度而有所不同。先前的研究已经探索了动力学机制其中tau(pl) tau(ps),而tau(pl) tau(ps)。在前者中,跨相凝胶在相分离之前出现,并且相分离很大程度上由活化驱动。在后者中,相分离首先发生在聚合物和非键分子之间,然后聚合物变成凝胶,因此驱动机理与通常的液-液混合过程相同。使用分子动力学模拟,我们在本文中探索了两个时间尺度可比的中间动力学机制。当通过热缩合反应进行聚合时,我们观察到了预期的交叉,一个是在早期的极限行为,然后是在后期的另一个极限行为。当通过自由基加成反应进行聚合时,结果表明驱动机理变化不止一次。 [参考:10]

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