ABSTRACT
Electrocoagulation (EC) using iron (Fe), zinc (Zn) and aluminum (Al) electrodes was comparatively applied in the treatment of selenium (Se) in flour production (FP) wastewater. It was indicated that EC treatment with Fe anode obtained highest removal efficiency (79.1%) for Se in the 90 min treatment in the comparative study, which could be attributed to the superior adsorption capacity of in-situ generated iron flocs. Removal of Se resulted from electrodeposition and adsorption to in-situ generated flocs in EC treatment, and the operational conditions significantly influenced the Se removal performance in this work. The results showed the acidic condition and higher current density favored EC treatment on Se removal, EC removed up to 97.8% of Se at pH 4 under 15 mA cm-2, whereas it obtained 83.5% and 50.4% of removal efficiency at pH 7 and 10, respectively. There was competitive adsorption in the process of selenium removal, as the in-situ generated flocs effectively removed 35.6% of humic acid-like (HA-like) substance in FP wastewater after 90 min treatment. The FTIR results showed that HA-like substance mainly contained the protein water hydrogen bond, carboxylate COO antisymmetric stretching and other functional groups. Through the analysis of existence of Se in flocs and wastewater, it can be found that approximately 2.8%-3.92% of Se was removed by electrodeposition process. This study illustrated the Se removal mechanism and provided constructive suggestion for food manufacturing to the metal removal and utilization of advanced treatment.
Subject(s)
Selenium , Water Purification , Aluminum/chemistry , Electrocoagulation , Electrodes , Flour , Hydrogen-Ion Concentration , Iron/chemistry , Wastewater/chemistry , Water Purification/methods , Zinc/chemistryABSTRACT
Ordered mesoporous carbon (OMC)-supported molybdenum carbide catalysts were successfully prepared in one pot using a solvent-evaporation-induced self-assembly strategy accompanied by a carbothermal hydrogen reduction reaction. Characterization with nitrogen sorption, small-angle XRD, and TEM confirmed that the obtained materials had high surface areas, large pore volumes, ordered mesoporous structures, narrow pore size distributions, and uniform dispersions of molybdenum carbide particles. With nitrogen replaced by hydrogen in the carbothermal reduction reaction, the formation temperature of molybdenum carbide could be reduced by more than 100 °C. By changing the amount of molybdenum precursor added from less than 2 % to more than 5 %, molybdenum carbide structures could be easily regulated from Mo(2) C to MoC. The catalytic performance of OMC-supported molybdenum carbide catalysts was evaluated by hydrodeoxygenation of vegetable oils. Compared with Mo(2)C, MoC exhibited high product selectivity and excellent resistance to leaching in the conversion of vegetable oils into diesel-like hydrocarbons.