Influence of the Electrolyte Type on the Adsorption and Electrokinetic Properties of the Ionic Polyamino Acids – Cr2O3 System

I. Ostolska, M. Wiśniewska
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引用次数: 1

Abstract

Abstract The influence of a kind of support electrolyte on the ionic polyamino acids adsorption at the chromium (III) oxide – polymer solution interface was investigated. The NaCl and CaCl2 were used as the background electrolytes. In order to determine the effect of the electrolyte, the same value of ionic strength of the test solutions were taken. It was proved that formation of intermolecular and intramolecular complexes in the presence of divalent calcium ions is responsible for essential changes in polymer adsorption. Related to the ionic character of polyamino acid two different adsorption behaviours can be observed. The increase of the ASP adsorption amount in the presence of calcium ions may be explained by formation of complexes between the dissociated carboxylic groups and Ca2+ ions. The opposite situation takes place in the case of polylysine – the application of CaCl2 results in the dramatic decrease in the polymer adsorption caused by blocking the active sites available for LYS macromolecules. In order to make a comprehensive analysis, the zeta potential and surface charge density measurements were performed taking into account the kind of the background electrolyte. The above-mentioned tests were carried out in the absence and presence of the polyamino acid at two different concentrations – 10 and 100 ppm respectively.
电解质类型对离子型多氨基酸- Cr2O3体系吸附及电动力学性能的影响
摘要研究了一种载体电解质对离子型多氨基酸在氧化铬-聚合物界面吸附的影响。采用NaCl和CaCl2作为背景电解质。为了确定电解质的影响,测试溶液的离子强度取相同的值。研究证明,在二价钙离子存在下,分子间和分子内复合物的形成是聚合物吸附发生本质变化的原因。与多氨基酸的离子性质有关,可以观察到两种不同的吸附行为。在钙离子存在的情况下,ASP吸附量的增加可能是由于解离羧基与Ca2+离子之间形成了配合物。在聚赖氨酸的情况下,相反的情况发生了——CaCl2的应用导致聚合物吸附急剧减少,这是由于阻断了LYS大分子可用的活性位点。为了进行全面的分析,考虑了背景电解质的种类,进行了zeta电位和表面电荷密度的测量。上述试验分别在10 ppm和100 ppm两种不同浓度的多氨基酸不存在和存在的情况下进行。
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