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Integrated bio-electrogenic process for bioelectricity production and cathodic nutrient recovery from azo dye wastewater
Affiliation:1. Engine Research Laboratory, Department of Mechanical Engineering, Indian Institute of Technology Kanpur, Kanpur 208016, India;2. Combustion Engine and Energy Conversion Laboratory, School of Mechanical Engineering, College of Engineering, Hanyang University, Seoul 133-791, Republic of Korea;1. Centre for Ocean Research, Sathyabama University, Jeppiaar Nagar, Rajiv Gandhi Road, Chennai 600119, Tamil Nadu, India;2. ESSO-National Institute of Ocean Technology (ESSO-NIOT), Pallikaranai, Chennai 600100, Tamil Nadu, India;1. Biotechnology Division, CSIR-National Institute for Interdisciplinary Science and Technology, Thiruvananthapuram 695019, Kerala, India;2. Academy of Scientific and Innovative Research (AcSIR), CSIR-NIIST, Thiruvananthapuram 695019, Kerala, India;1. Thermo-catalytic Processes Area (TPA), Bio-Fuels Division (BFD), CSIR-Indian Institute of Petroleum (IIP), Dehradun 248005, India;2. Academy of Scientific and Innovative Research (AcSIR), New Delhi, India;1. Engine Research Laboratory, Department of Mechanical Engineering, Indian Institute of Technology Kanpur, Kanpur 208016, India;2. Department of Civil Engineering, Indian Institute of Technology Kanpur, Kanpur 208016, India
Abstract:Microbial electrochemical treatment (MET) process was designed to evaluate complete mineralization of partially treated dye effluent obtained from anoxically operated Periodic discontinuous batch reactor (PDBR) for simultaneous bioelectricity generation and recovery of nutrients. In MET bioreactor, anode and cathode chambers were fed with designed synthetic wastewater (DSW) and PDBR dye effluents. The dye metabolite (NH4+) will be converted to nitrates by the activity of aerobic biocatalyst present in cathode chamber to be used as biofertilizer. Dye removal of 90.2% was observed with good electrogenic activity (voltage (OCV)/current; 395 mV/1.77 mA). The mineralization of dye and its intermediates were assessed by reduction in overall toxicity from 23% to 4%. Chemical oxygen demand (COD) removal efficiency of 75% (anode) and 88% (cathode) were observed in correspondence to higher azoreductase (18.7 U; 48 h) and dehydrogenase (1.66 μg/ml of toluene; 24 h) enzyme activities which correlated well with metabolic activities of biocatalyst. Bioelectrocatalytic behavior of mixed biocatalyst on the basis of redox catalytic currents and prevalence of redox mediators signified the specific function of electron transfer toward dye mineralization. The results obtained suggest that the use of MET can considerably degrade toxic pollutants and provides nitrate rich solution (biofertilizer). Utilization of recovered nutrients directly to farms without any energy intensive methods is reported in this communication.
Keywords:Microbial electrochemical treatment (MET)  Periodic discontinuous batch reactor (PDBR)  Bioremediation  Nitrate flux  Biofertilizer
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