Transition Behavior of Polyelectrolyte Brushes Depending on Polymer Chain Density

S. Hayashi, T. Abe, N. Higashi, M. Niwa, K. Kurihara
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引用次数: 1

Abstract

Abstract Brush layers of polyelectrolytes, ionized poly(L-lysine) (PLL) or poly(L-glutamic acid) (PLGA), at desired densities were prepared by the Langmuir-Blodgett (LB) deposition of amphiphiles bearing PLL or PLGA segments as hydrophilic groups, and subjected to the surface force measurements. Abrupt changes in the surface force, the surface potential, and the transfer ratio of the brush layers were observed at a critical density. The present data is in good agreement with our previous report on the jump in the compressibility of the brushes, and supports the existence of the density dependent transition of polyelectrolytes in solutions.
聚合物链密度对聚电解质电刷过渡行为的影响
摘要:采用Langmuir-Blodgett (LB)沉积方法,以聚l -赖氨酸(PLL)或聚l -谷氨酸(PLGA)为亲水性基团,制备了具有理想密度的聚电解质(离子化聚l -赖氨酸)或聚l -谷氨酸(PLGA))刷状层,并进行了表面力测量。在临界密度下,表面力、表面电位和电刷层的传递比发生了突变。目前的数据与我们之前关于电刷可压缩性跳跃的报告很好地一致,并支持溶液中聚电解质的密度依赖转变的存在。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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