Thermodynamics of binding interactions between extracellular polymeric substances and heavy metals by isothermal titration microcalorimetry

被引:76
|
作者
Yan, Peng [1 ,2 ]
Xia, Jia-Shuai [3 ]
Chen, You-Peng [1 ,2 ]
Liu, Zhi-Ping [3 ]
Guo, Jin-Song [1 ,2 ]
Shen, Yu [1 ,2 ]
Zhang, Cheng-Cheng [3 ]
Wang, Jing [4 ]
机构
[1] Chinese Acad Sci, Chongqing Inst Green & Intelligent Technol, Chongqing 400714, Peoples R China
[2] Chinese Acad Sci, Key Lab Reservoir Aquat Environm, Chongqing 400714, Peoples R China
[3] Chongqing Univ, Key Lab Three Gorges Reservoir Regions Ecoenviron, Chongqing 400045, Peoples R China
[4] Chongqing Jianzhu Coll, Chongqing 400072, Peoples R China
基金
中国国家自然科学基金;
关键词
Extracellular polymeric substances; Heavy metals; Isothermal titration calorimetry; Biosorption; EPS; CALORIMETRY; BIOSORPTION; PROTEINS; REMOVAL; SLUDGES; ROLES; PH;
D O I
10.1016/j.biortech.2017.02.067
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
Extracellular polymeric substances (EPS) play a crucial role in heavy metal bio-adsorption using activated sludge, but the interaction mechanism between heavy metals and EPS remains unclear. Isothermal titration calorimetry was employed to illuminate the mechanism in this study. The results indicate that binding between heavy metals and EPS is spontaneous and driven mainly by enthalpy change. Extracellular proteins in EPS are major participants in the binding process. Environmental conditions have significant impact on the adsorption performance. Divalent and trivalent cations severely impeded the binding of heavy metal ions to EPS. Electrostatic interaction mainly attributed to competition between divalent cations and heavy metal ions; trivalent cations directly competed with heavy metal ions for EPS binding sites. Trivalent cations were more competitive than divalent cations for heavy metal ion binding because they formed complexing bonds. This study facilitates a better understanding about the interaction between heavy metals and EPS in wastewater treatment. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:354 / 363
页数:10
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