重新探讨了静电稳定溶致层状相的层压缩模量:应用于聚合物诱导的SmA-SmA临界相分离的定量分析

L. Porcar, C. Ligoure, J. Marignan
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引用次数: 11

摘要

我们提出了静电作用稳定的溶致层状相的近晶压缩模量B的计算方法。这个基于泊松-玻尔兹曼方程数值解的计算表明,在两个渐近极限(无添加盐或大添加盐浓度)下,文献中给出的经典解析表达式B仅在非常严格的条件下有效。本研究的动机在于了解由非离子表面活性剂(Triton X100/Triton X35)、阳离子表面活性剂(十六烷基吡啶氯)、水、癸烷和水溶性聚合物(聚乙烯基吡啶酮)混合形成的掺杂两亲性片层相的物理行为。在我们的系统中观察到的临界层状/层状相分离可以通过使用当前的计算和Ligoure等人提出的最近的模型来定量地解释,该模型预测了聚合物介导的膜间相互作用对近晶压缩模量的贡献。
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Layer compression modulus of electrostatically stabilized lyotropic lamellar phases revisited : Application to the quantitative analysis of a polymer induced critical SmA-SmA phase separation
We present a calculation of the smectic compression modulus B of a lyotropic lamellar phase stabilized by electrostatic interactions. This calculation, based on a numerical solution of the Poisson-Boltzmann equation, shows that the classical analytical expressions of B given in the literature in the two asymptotic limits (absence of added salt, or large added salt concentration) are valid under very restrictive conditions only. The motivation of this study lies in the understanding of the physical behavior of a doped amphiphilic lamellar phase formed from a mixture of non ionic surfactants (Triton X100/Triton X35), cationic surfactant (cetylpyridinium chloride), water, decane and water-soluble polymer (polyvynilpyrolidone). A critical lamellar/lamellar phase separation observed in our system is quantitatively well-explained by using both the present calculations and a recent model proposed by Ligoure et al. which predicts the polymer-mediated intermembrane interaction contribution to the smectic compression modulus.
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