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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:已知链端对聚合物熔体的表面具有熵偏好,这反过来会导致多分散熔体的短链分离到表面。在这里,我们使用自洽场理论(SCFT)研究了短聚合物和长聚合物双组分熔体的熵偏析。单独的聚合物由离散单体建模,该离散单体通过统计长度A的自由接合键连接,并且调整场以产生宽度席XI的指定表面轮廓。推导了短聚合物过量浓度δφ(s)(z)、积分过量θ(s)和表面张力的熵效应γ(en)的半解析表达式,并用数值SCFT进行了测试。这些表达式表现出对分子量分布的普遍依赖性,具有模型依赖系数。通常,必须对数值进行数值计算,但它们可以在一次席上大于或大于a时近似地解析。我们说明了这一点是如何用来推导不混溶的A型和B型多分散均聚物之间的界面张力的简单表达式。

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