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Layer-by-layer adsorption of polyelectrolyte and surfactant and adsorption of their complexes on solid surface

机译:聚电解质和表面活性剂的分层吸附以及它们的配合物在固体表面上的吸附

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摘要

The capillary electrokinetics method (measurement of streaming potential and current in a cap- illary with a radius of 5-7 μm made of fused quartz) is employed to study the structure formation at interfaces between quartz and solutions containing a cationic polyelectrolyte (poly(diallyldimethylammonium chloride) with molecular mass M = 100000-200000) and an anionic surfactant (sodium dodecyl sulfate). The kinetics of surface layer formation is studied upon the layer-by-layer adsorption of the components and the adsorption of their complexes at the same component ratios. It is established that the formation time and the electrokinetic potentials of the surface layers are almost independent of the procedure of their formation. In the case of the layer-by-layer adsorption, the first layers of the polyelectrolyte appear to be virtually undeformed, thus indicating that molecules with a planar conformation prevail in the adsorption layer. Surfactant adsorption enhances the deformation (layer loosening), which decreases with time (layer aging). Layers formed from the complexes have a denser (less deformable) structure. Variations in the electrokinetic potentials of the layers during the long-term pumping of a background electrolyte solution through a capillary witnesses the prevailing desorption of the anionic surfactant, with the desorption being noticeably more pronounced for the layers resultant from the adsorption of the complexes.
机译:毛细管电动力学方法(测量由熔融石英制成的半径为5-7μm的毛细管中的流动电势和电流)用于研究石英与含有阳离子聚电解质(聚(二烯丙基二甲基铵)的溶液)之间的界面处的结构形成。分子质量M = 100000-200000)和阴离子表面活性剂(十二烷基硫酸钠)。在组分的逐层吸附及其在相同组分比例下的配合物吸附时,研究了表面层形成的动力学。已经确定,表面层的形成时间和电动势几乎与它们的形成过程无关。在逐层吸附的情况下,聚电解质的第一层似乎实际上未变形,因此表明在吸附层中存在具有平面构型的分子。表面活性剂的吸附会增强变形(层松动),并随时间减少(层老化)。由复合物形成的层具有较致密的(较不易变形的)结构。在通过毛细管长期泵送背景电解质溶液期间,各层的电动势的变化见证了阴离子表面活性剂的普遍解吸,对于由络合物的吸附产生的层,解吸更为明显。

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