Influence of ionic strength, anions, cations, and natural organic matter on the adsorption of pharmaceuticals to silica

被引:146
作者
Bui, Tung Xuan [1 ]
Choi, Heechul [1 ]
机构
[1] GIST, Dept Environm Sci & Engn, Kwangju 500712, South Korea
基金
新加坡国家研究基金会;
关键词
Adsorption; Pharmaceuticals; Silica; Ionic strength; Cations; Natural organic matter; MOLECULAR-STRUCTURE; HUMIC SUBSTANCES; TETRACYCLINE; SORPTION; FATE; ALUMINUM; CLAY; OXYTETRACYCLINE; CIPROFLOXACIN; ENVIRONMENT;
D O I
10.1016/j.chemosphere.2010.05.046
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The adsorption of four wide-use pharmaceuticals (carbamazepine, diclofenac, ibuprofen, and ketoprofen) onto a porous silica was investigated under varied ionic strengths, different anions, divalent cations (Ca2+ and Mg2+), trivalent cations (Al3+ and Fe3+), and natural organic matter (NOM). The experiments demonstrated that at a given pH the adsorption was most affected by ionic strength, trivalent cations, and properties of pharmaceuticals. The increase of ionic strength resulted in an increase in the adsorption of ketoprofen, but a decrease in the adsorption of carbamazepine. Trivalent metal cations made intense increases in the adsorption of three acidic pharmaceuticals, which could be due to the formation of inner-sphere complex of the cations on the surface and/or complexation of the pharmaceuticals with both surface and aqueous metal species. It was found that the adsorption of carbamazepine was not affected by divalent and trivalent cations, whereas the adsorption of diclofenac was solely impacted by the presence of Al3+. Moreover, divalent cations at low concentration could slightly enhance the adsorption of ibuprofen and ketoprofen, whereas NOM caused a reduction in the adsorption of the tested pharmaceuticals except for diclofenac. These results suggest that ionic strength, divalent cations, trivalent cations, and NOM are notable factors affecting the adsorption of pharmaceuticals and thus the ultimate fate of pharmaceuticals in the aqueous environment. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:681 / 686
页数:6
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