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碱金属离子介导的聚环氧乙烷在带电表面的选择性吸附。

Selective adsorption of poly(ethylene oxide) onto a charged surface mediated by alkali metal ions.

作者信息

Chai Liraz, Goldberg Ronit, Kampf Nir, Klein Jacob

机构信息

Materials and Interfaces Department, Weizmann Institute of Science, Rehovot, Israel.

出版信息

Langmuir. 2008 Feb 19;24(4):1570-6. doi: 10.1021/la702514j. Epub 2007 Dec 7.

Abstract

Using a surface force balance, we have measured normal and shear interactions between mica surfaces across pure water and across 0.1 M aqueous solutions of LiNO3, NaNO3, KNO3, and CsNO3, both prior to adding polymer and following addition of 1.5 x 10(-4) w/w poly(ethylene oxide) (PEO, Mw = 170 kD) and overnight incubation. Our results reveal that while the PEO adsorbs strongly from the KNO3 and CsNO3 solutions, unexpectedly it does not adsorb at all from the LiNO3 and NaNO3 salt solutions. We attribute this to the different nature of the hydration layers about the alkali metal ions: these favor liganding to the negatively charged mica surface of the etheric -O- group on the ethylene oxide monomer for the case of the more weakly hydrated K+ and Cs+, but not for the case of Na+ or Li+ with their more strongly bound water. A simple model relating the electrostatic energy changes occurring upon such liganding to the experimentally measured hydration energies of the different alkali metal ions supports this attribution.

摘要

使用表面力天平,我们测量了云母表面在纯水以及0.1M硝酸锂、硝酸钠、硝酸钾和硝酸铯水溶液中的法向和剪切相互作用,测量分别在添加聚合物之前以及添加1.5×10⁻⁴w/w聚环氧乙烷(PEO,Mw = 170 kD)并孵育过夜之后进行。我们的结果表明,虽然PEO从硝酸钾和硝酸铯溶液中强烈吸附,但出乎意料的是,它根本不从硝酸锂和硝酸钠盐溶液中吸附。我们将此归因于碱金属离子周围水化层的不同性质:对于水化较弱的K⁺和Cs⁺,这些离子有利于与环氧乙烷单体上带负电荷的云母表面的醚基-O-配位,但对于Na⁺或Li⁺及其结合更紧密的水则不然。一个将这种配位时发生的静电能变化与不同碱金属离子的实验测量水化能相关联的简单模型支持了这一归因。

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