The thermodynamic stability of the mixtures of hyperbranched poly(ethyleneimine) and sodium dodecyl sulfate at low surfactant-to-polyelectrolyte ratios

被引:13
|
作者
Meszaros, Robert [1 ]
机构
[1] Eotvos Lorand Univ, Inst Chem, Lab Interfaces & Nanosized Syst, H-1117 Budapest, Hungary
关键词
Polyelectrolyte; Surfactant; Colloidal dispersion; Thermodynamic stability; Kinetic stability; OPPOSITELY CHARGED SURFACTANT; CATIONIC SURFACTANT; SALT CONCENTRATION; AQUEOUS-SOLUTIONS; MIXING PROTOCOL; PHASE-BEHAVIOR; COMPLEXES; SCATTERING; POLYETHYLENIMINE; ADSORPTION;
D O I
10.1016/j.jcis.2009.06.053
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
The equilibrium nature of the association between the hyperbranched poly(ethyleneimine) (PEI) and sodium dodecyl sulfate (SDS) has been investigated in the presence of excess polyelectrolyte. It was found that the thermodynamic stability of the system considerably depends on the ionization degree of the PEI molecules. In the case of slightly charged PEI molecules, the PEI/SDS mixtures are thermodynamically stable solutions in the pre-precipitation concentration range. In contrast, at low and moderate pH kinetically stable colloidal dispersions of the positively charged PEI/SDS particles can be observed at low surfactant-to-polyelectrolyte ratios. These dispersions are stabilized by the uncompensated charges of the PEI molecules. In addition to the primary PEI/SDS particles, larger aggregates may also appear in the mixtures. The higher the protonation degree of the PEI molecules and the smaller the net charge of the primary PEI/SDS particles, the more likely the aggregate formation becomes. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:444 / 449
页数:6
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