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Adsorption of sulfonamides on lake sediments |
Zhenxing ZHONG1,2, Jian XU1,3, Yuan ZHANG1,3( ), Lei LI1,3, Changsheng GUO1,3, Yan HE1,3, Wenhong FAN4, Beiping ZHANG2 |
| 1. State Key Laboratory of Environmental Criteria and Risk Assessment, Chinese Research Academy of Environmental Sciences, Beijing 100012, China; 2. School of Environmental Science and Engineering, Huazhong University of Science & Technology, Wuhan 430074, China; 3. Laboratory of Riverine Ecological Conservation and Technology, Chinese Research Academy of Environmental Sciences, Beijing 100012, China; 4. Department of Environmental Science and Engineering, School of Chemistry and Environment, Beihang University, Beijing 100191, China |
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Abstract Sulfonamides (SAs) are one class of the most widely used antibiotics around the world. Their fate and transport in the aquatic environment is of great concern. In this study, adsorption of four SAs—sulfadiazine (SD), sulfamethoxazole (SMZ), sulfadimethoxine (SDM) and sulfamethazine (SM2)—in single-solute and multi-solute systems on sediments of Dianchi (DC) Lake and Taihu (TH) Lake, China was investigated with batch experiments. In the single-solute adsorption system, the Langmuir model and the dual-mode model described the adsorption process better than the Freundlich model. Model fitness was better on DC sediment than on TH sediment. The order of adsorption capacity approximately followed a decreasing order of SDM>SD>SM2>SMZ on both sediments, which was likely attributed to the distinctly different water solubility of the four SAs. In the multi-solute system, the order of adsorption capacity was SM2>SDM>SD>SMZ, which was probably related to the compound speciation caused by the pH values of the experimental solution. In the multi-solute system, both competitive and cooperative adsorption played important roles in the adsorption of sulfonamides on sediments.
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| Keywords
sulfonamides
sediments
competitive adsorption
cooperative adsorption
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Corresponding Author(s):
ZHANG Yuan,Email:zhangyuan@craes.org.cn
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Issue Date: 01 August 2013
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