Direct determination of the thermodynamics of polyelectrolyte complexation and implications thereof for electrostatic layer-by-layer assembly of multilayer films

被引:57
作者
Bharadwaj, Satish [1 ]
Montazeri, Reza [1 ]
Haynie, Donald T. [1 ]
机构
[1] Louisiana Tech Univ, Bionanosyst Engn Lab, Ruston, LA 71272 USA
关键词
D O I
10.1021/la0518391
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Interpolyelectrolyte complex (IPEC) formation between poly(styrene sulfonate) (PSS) and poly(allylamine hydrochloride) (PAH) has been studied over a range of ionic strengths by isothermal titration calorimetry (ITC), turbidity titration, and electrostatic layer-by-layer assembly (ELBL). The results indicate that IPEC formation of PSS/PAH in aqueous solution is predominantly entropy-driven. The thermodynamic parameters suggest the formation of different types of complexes and aggregates due to salt-induced conformational changes in the polyelectrolyte conformation. Differences in polyelectrolyte behavior in the different salt-concentration regimes are described in terms of changes in the Debye screening length of the polyelectrolytes. The relationship of the results to the effect of salt concentration on the assembly of polyelectrolyte multilayer films (PEMs) is discussed.
引用
收藏
页码:6093 / 6101
页数:9
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