Oscillatory packing and depletion of polyelectrolyte molecules at an oxide-water interface

被引:54
作者
Biggs, S
Dagastine, RR
Prieve, DC
机构
[1] Univ Newcastle, Chem Discipline, Sch Environm & Life Sci, SRC Multiphase Proc, Callaghan, NSW 2308, Australia
[2] Carnegie Mellon Univ, Dept Chem Engn, Pittsburgh, PA 15213 USA
[3] Carnegie Mellon Univ, Colloids Polymers & Surfaces Program, Pittsburgh, PA 15213 USA
关键词
D O I
10.1021/jp026425k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Total internal reflection microscopy (TIRM) has been used to,study the interactions between a 5 mum borosilicate glass sphere and a silica slide in the presence of a nonadsorbing polyelectrolyte, sodium (polystyrene sulfonate) (NaPSS). The effect of the polymer concentration, within the dilute solution regime, on the observed interactions was investigated. In all cases, the interactions displayed a short-range electrostatic repulsion followed immediately, at larger separations, by a decaying oscillatory interaction that is attributed to structuring of the polyelectrolyte in solution. The periodicity of the oscillations, as a function of concentration, indicates that at large surface separations the polymer chains are ordered as a nonintermixing, space-filling, latex. At polymer concentrations of between 200 and 1000 ppm, a transition to a system of ordered rods, parallel to the interface was seen for the final layer of polymer molecules.
引用
收藏
页码:11557 / 11564
页数:8
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