Structuring of poly(DADMAC) chains in aqueous media: a comparison between bulk and free-standing film measurements

被引:56
|
作者
von Klitzing, R
Kolaric, B
Jaeger, W
Brandt, A
机构
[1] Tech Univ Berlin, Stranski Lab Phys & Theoret Chem, D-10623 Berlin, Germany
[2] Hahn Meitner Inst Berlin GmbH, D-14109 Berlin, Germany
[3] Fraunhofer Inst Angew Polymerforsch, D-14476 Golm, Germany
关键词
D O I
10.1039/b106929m
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
Recently, thin film balance (TFB) measurements have shown that foam films (thickness 5-120 nm) containing polyelectrolytes thin stepwise. This was connected to the ordering of the polyelectrolyte chains in the film, since pure foam films thin in a continuous way. The present paper shows disjoining pressure isotherms of films containing the polycation poly(DADMAC) and small angle neutron scattering (SANS) spectra of the corresponding aqueous solutions at different polyelectrolyte concentrations. The steps Deltah in the isotherms are of the same size as the correlation length xi in the bulk solution. This leads to the conclusion that the interactions between the polyelectrolyte chains which are responsible for their structuring in the bulk determines also the strati cation behavior of polyelectrolyte/surfactant films. These findings were confirmed by the influence of further parameters like the molecular weight, the ionic strength and the degree of charge. The results of the TFB measurements and the SANS experiments show the same dependence on these parameters.
引用
收藏
页码:1907 / 1914
页数:8
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