Adsorption/photo-electrodialysis combination system for Pb2+ removal using bentonite/membrane/semiconductor

被引:31
作者
Hamane, D. [1 ]
Arous, O. [3 ,4 ]
Kaouah, F. [1 ]
Trari, M. [2 ]
Kerdjoudj, H. [4 ]
Bendjama, Z. [1 ]
机构
[1] USTHB, Fac Chem Engn, Lab Sci Genie Procedes Ind, Algiers, Algeria
[2] USTHB, Fac Chem, Lab Storage & Valorizat Renewable Energies, Algiers, Algeria
[3] Ctr Res Phys & Chem Anal CRAPC, BP 248, Algiers 16004, RP, Algeria
[4] USTHB, Fac Chem, Lab Hydrometallurgy & Inorgan Mol Chem, Algiers, Algeria
来源
JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING | 2015年 / 3卷 / 01期
关键词
Adsorption; Bentonite; Lead; Membrane; Photo-electrodialysis;
D O I
10.1016/j.jece.2014.11.003
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A combination system combining adsorption/photo electrochemistry/dialysis is investigated for the first time for the Pb2+ removal. The Pb2+ adsorption on the Algerian bentonite is studied in batch mode. The initial Pb2+ concentration, adsorption dosage, pH and temperature are optimized. The maximum removal is observed at pH 6 for a concentration of 100mg L (-1) at 25 degrees C. The adsorption is fast with similar to 90% occurring within 40 min of contact time. The process is spontaneous and endothermic. The Langmuir model is successfully applied to fit the experimental data. The remaining concentration is lowered by photo-electrodialysis below the threshold required by the water standards. The ion exchange membrane, configured as a horizontal electrode, is an essential part of the process. The membrane is polymerized from cellulose triacetate modified by poly-ethyleneimine and plasticized by 2-nitrophenyl pentyl ether. It is characterized by FTIR and thermal analysis (TGA). The photo-electrodialysis indicates that the combined system p-CuCrO2/membrane/n-Sr2Fe2O5 enhances considerably the electrons transfer and the diffusion flux of Pb2+. 35 percent of Pb2+ are photo-electrochemically reduced under artificial light. The rate conversion increases up to 86% under solar light. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:60 / 69
页数:10
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