Department of Chemical Technology, Chemical Faculty, Gdańsk University of Technology, ul. Narutowicza 11/12, 80-233 Gdańsk, Poland.
Chemosphere. 2013 Jan;90(2):706-12. doi: 10.1016/j.chemosphere.2012.09.053. Epub 2012 Oct 15.
As the amount of industrial processes involving ionic liquids (ILs) increase the question of their environmental fate awaits an answer. Should ILs become a source of pollution they will primarily be found in soils and water. Interaction of imidazolium IL with soils is a complex interplay of many parameters making predicting their fate and mobility a challenging task. In order to shed more light on the mechanism of adsorption in soils we examined the interactions of imidazolium ILs with the major component of soils, namely mineral fraction. Within this work adsorption on kaolinite and quartz was investigated in terms of adsorption isotherms, partition coefficients and changes of zeta potentials of clays modified by ILs aggregates. The zeta potential was found to be dependent on the alkyl chain length of the imidazolium homologues. It can therefore be concluded that although adsorption seems to rely on electrostatic attraction, at least in the initial stage, the hydrophobicity of molecules is just as significant.
随着涉及离子液体 (ILs) 的工业过程数量的增加,它们的环境命运问题亟待解答。如果 ILs 成为污染的来源,它们主要将存在于土壤和水中。离子液体与土壤的相互作用是许多参数的复杂相互作用,使得预测它们的命运和迁移成为一项具有挑战性的任务。为了更深入地了解土壤中吸附的机制,我们研究了离子液体与土壤主要成分,即矿物质部分的相互作用。在这项工作中,我们研究了在高岭石和石英上的吸附等温线、分配系数以及 ILs 团聚体改性粘土的 ζ 电位变化,研究了离子液体在这些矿物上的吸附。发现 ζ 电位取决于离子液体同系物的烷基链长度。因此可以得出结论,尽管吸附似乎依赖于静电吸引,但至少在初始阶段,分子的疏水性同样重要。