Adsorption of microcystin-LR onto kaolinite, illite and montmorillonite

被引:26
|
作者
Liu, Yen-Ling [1 ]
Walker, Harold W. [2 ]
Lenhart, John J. [1 ]
机构
[1] Ohio State Univ, Dept Civil Environm & Geodet Engn, Columbus, OH 43210 USA
[2] SUNY Stony Brook, Dept Civil Engn, Stony Brook, NY 11794 USA
基金
美国海洋和大气管理局;
关键词
Clay; Cyanotoxin; Linear isotherm; Fate; HARMFUL ALGAL BLOOMS; HUMIC-ACID; CYANOBACTERIAL HEPATOTOXINS; CLAY-MINERALS; FRESH-WATER; SEASONAL-VARIATION; ORGANIC-COMPOUNDS; SURFACE-CHARGE; ATR-FTIR; MECHANISMS;
D O I
10.1016/j.chemosphere.2018.12.137
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In this study, microcystin-LR (MCLR) interactions with three representative silicate clays were studied using equilibrium batch experiments in order to provide insight into the role of clays on determining MCLR fate. The three tested clay minerals (kaolinite, montmorillonite and illite), saturated with sodium or calcium ions, were equilibrated with MCLR across a range of toxin concentrations at pH 5, 7 or 9. The results were fit to Freundlich and linear isotherm models, with the linear isotherm fits deemed most appropriate. In general, adsorption of MCLR was greater in the systems with Ca than in those with Na, however, regardless of the cation present, montmorillonite had the highest adsorption affinity for MCLR. Furthermore, except for Ca-montmorillonite, MCLR adsorption decreased with increasing pH. The pH dependence of adsorption suggests the polar groups of MCLR, carboxylate associated with the glutamic acid and methylaspartic acid groups and amine associated with the arginine group, were more important in determining MCLR interactions with clays than the nonpolar ADDA group. Increased adsorption in systems enriched with calcium suggests Ca modified the clay interfacial properties and the availability of MCLR groups in a manner that increased MCLR affinity. Overall, the results suggest clays are capable of adsorbing MCLR from the aqueous phase, particularly at low pH and when saturated with Ca2+. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:696 / 705
页数:10
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