Adsorptive removal of selected pharmaceuticals by mesoporous silica SBA-15

被引:317
|
作者
Bui, Tung Xuan [1 ]
Choi, Heechul [1 ]
机构
[1] Gwangju Inst Sci & Technol GIST, Dept Environm Sci & Engn, Kwangju 500712, South Korea
关键词
Removal; Adsorption; Mesoporous silica SBA-15; Pharmaceuticals; Surface water; DRINKING-WATER TREATMENT; SEWAGE-TREATMENT PLANTS; AQUEOUS-SOLUTION; SURFACE WATERS; FATE; IBUPROFEN; NAPROXEN; SORPTION; ALUMINA; MCM-41;
D O I
10.1016/j.jhazmat.2009.02.072
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The removal of five selected pharmaceuticals, viz., carbamazepine, clofibric acid, diclofenac, ibuprofen, and ketoprofen was examined by batch sorption experiments onto a synthesized mesoporous silica SBA-15. SBA-15 was synthesized and characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), N-2 adsorption-desorption measurement, and point of zero charge (PZC) measurement. Pharmaceutical adsorption kinetics was rapid and occurred on a scale of minutes, following a pseudo-second-order rate expression. Adsorption isotherms were best fitted by the Freundlich isotherm model. High removal rates of individual pharmaceuticals were achieved in acidic media (pH 3-5) and reached 85.2% for carbamazepine, 88.3% for diclofenac, 93.0% for ibuprofen, 94.3% for ketoprofen, and 49.0% for clofibric acid at pH 3 but decreased with increase in pH. SBA-15 also showed high efficiency for removal of a mixture of 5 pharmaceuticals. Except for cloflbric acid (35.6%), the removal of pharmaceuticals in the mixture ranged from 75.2 to 89.3%. Based on adsorption and desorption results, the mechanism of the selected pharmaceuticals was found to be a hydrophilic interaction, providing valuable information for further studies to design materials for the purpose. The results of this study suggest that mesoporous-silica-based materials are promising adsorbents for removing pharmaceuticals from not only surface water but also wastewater of pharmaceutical industrial manufactures. (c) 2009 Published by Elsevier B.V.
引用
收藏
页码:602 / 608
页数:7
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