Removal mechanism for chromium (VI) in groundwater with cost-effective iron-air fuel cell electrocoagulation

被引:37
作者
Maitlo, Hubdar Ali [1 ]
Kim, Ki-Hyun [1 ]
Park, Joo Yang [1 ]
Kim, Jung Hwan [1 ]
机构
[1] Hanyang Univ, Dept Civil & Environm Engn, 222 Wangsimni Ro, Seoul 04763, South Korea
基金
新加坡国家研究基金会;
关键词
IAFCEC; Cr(VI) removal; Interfering ions; Power generation; Operating cost; ELECTROPLATING WASTE-WATER; X-RAY-ABSORPTION; HEXAVALENT CHROMIUM; PHOTOCATALYTIC REDUCTION; COMPETITIVE ADSORPTION; AQUEOUS-SOLUTION; CR(VI) REMOVAL; ELECTRICITY-GENERATION; POWER-GENERATION; OPERATING COST;
D O I
10.1016/j.seppur.2018.12.058
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Metal-air fuel cell electrocoagulation is one of the most cost-effective and innovative treatment options for metals in water. Here, the removal mechanism of chromium (Cr(VI)) was assessed using an iron-air fuel cell electrocoagulation (IAFCEC) system. Simultaneously, the effects of such treatment were also investigated with respect to a list of parameters controlling groundwater quality. During the IAFCEC operation, in-situ production of stable iron hydroxides (e.g., maghemite, hematite, and goethite) was experienced due to the sacrificial oxidation of the iron anode electrode. Therefore, these iron hydroxides were responsible for direct co-precipitation of aqueous Cr(VI). The removal efficiency of the system was assessed by varying the initial concentrations of Cr(VI) such as 1, 5, and 10 mg L-1). The IAFCEC, when operated with low concentrations of competing anions (e.g., silicate, phosphate, magnesium, and calcium), was capable of treating 6 L of water containing 1 mg L-1 Cr(VI) per day with an operating cost of 0.2 USD m(-3). This study demonstrates the IAFCEC as one of the most cost-effective treatment methods for Cr(VI) removal based on evaluation of performance relative to other options commonly available.
引用
收藏
页码:378 / 388
页数:11
相关论文
共 106 条
[1]   Removal of Cr(VI) from polluted solutions by electrocoagulation: Modeling of experimental results using artificial neural network [J].
Aber, S. ;
Amani-Ghadim, A. R. ;
Mirzajani, V. .
JOURNAL OF HAZARDOUS MATERIALS, 2009, 171 (1-3) :484-490
[2]   Treatment of electroplating wastewater containing Cu2+, Zn2+ and Cr(VI) by electrocoagulation [J].
Adhoum, N ;
Monser, L ;
Bellakhal, N ;
Belgaied, JE .
JOURNAL OF HAZARDOUS MATERIALS, 2004, 112 (03) :207-213
[3]   Sorption of Cr(VI) onto natural iron and aluminum (oxy)hydroxides: Effects of pH, ionic strength and initial concentration [J].
Ajouyed, Omar ;
Hurel, Charlotte ;
Ammari, Mohammed ;
Ben Allal, Laila ;
Marmier, Nicolas .
JOURNAL OF HAZARDOUS MATERIALS, 2010, 174 (1-3) :616-622
[4]   Copper, chromium and nickel removal from metal plating wastewater by electrocoagulation [J].
Akbal, Feryal ;
Camci, Selva .
DESALINATION, 2011, 269 (1-3) :214-222
[5]  
Andrade A. L., 2009, Cerâmica, V55, P420
[6]   Kinetics and adsorption isotherm for the removal of fluoride and chromium (VI) from wastewater by electrocoagulation [J].
Aoudj, S. ;
Cheknane, B. ;
Zemmouri, H. ;
Zermane, F. ;
Khelifa, A. ;
Hecini, M. ;
Drouiche, N. .
DESALINATION AND WATER TREATMENT, 2017, 82 :262-270
[7]   Effect of pH and chloride concentration on the removal of hexavalent chromium in a batch electrocoagulation reactor [J].
Arroyo, M. G. ;
Perez-Herranz, V. ;
Montanes, M. T. ;
Garcia-Anton, J. ;
Guinon, J. L. .
JOURNAL OF HAZARDOUS MATERIALS, 2009, 169 (1-3) :1127-1133
[8]   Photocatalytic degradation of hexavalent chromium emerging contaminant via advanced titanium dioxide nanostructures [J].
Athanasekou, C. ;
Romanos, G. Em. ;
Papageorgiou, S. K. ;
Manolis, G. K. ;
Katsaros, F. ;
Falaras, P. .
CHEMICAL ENGINEERING JOURNAL, 2017, 318 :171-180
[9]   ADSORPTION OF CHROMIUM ION (VI) BY ACID ACTIVATED CARBON [J].
Attia, A. A. ;
Khedr, S. A. ;
Elkholy, S. A. .
BRAZILIAN JOURNAL OF CHEMICAL ENGINEERING, 2010, 27 (01) :183-193
[10]   Cr(VI) removal from synthetic wastewater using coconut shell charcoal and commercial activated carbon modified with oxidizing agents and/or chitosan [J].
Babel, S ;
Kurniawan, TA .
CHEMOSPHERE, 2004, 54 (07) :951-967