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Entropic segregation of short polymers to the surface of a polydisperse melt

机译:短聚合物对多分散熔体表面的熵偏析

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Chain ends are known to have an entropic preference for the surface of a polymer melt, which in turn is expected to cause the short chains of a polydisperse melt to segregate to the surface. Here, we examine this entropic segregation for a bidisperse melt of short and long polymers, using self-consistent field theory (SCFT). The individual polymers are modeled by discrete monomers connected by freely-jointed bonds of statistical length a, and the field is adjusted so as to produce a specified surface profile of width xi. Semi-analytical expressions for the excess concentration of short polymers, delta phi(s)(z), the integrated excess, theta(s), and the entropic effect on the surface tension, gamma(en), are derived and tested against the numerical SCFT. The expressions exhibit universal dependences on the molecular-weight distribution with model-dependent coefficients. In general, the coefficients have to be evaluated numerically, but they can be approximated analytically once xi greater than or similar to a. We illustrate how this can be used to derive a simple expression for the interfacial tension between immiscible A- and B-type polydisperse homopolymers.
机译:已知链末端具有对聚合物熔体表面的熵偏好,这又预期导致多分散熔体的短链以分离到表面。在此,我们使用自洽的场理论(SCFT)来检查用于短和长聚合物的双重熔体的这种熵偏析。各种聚合物由通过统计长度A的自由接合键连接的离散单体进行建模,并且调节该领域以产生宽度Xi的指定表面轮廓。用于过量浓度的短聚合物,δPHI(Z),综合过量,θ,熵对表面张力,γ(en)的熵表达,并测试和测试数值SCFT。表达表现出对具有模型依赖系数的分子量分布的通用依赖性。通常,必须数值评估系数,但是每种大于或类似于a的xi,它们可以分析地近似。我们说明了如何用于推导出在不混溶的A-和B型多分散均聚物之间的界面张力的简单表达。

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