Yining Hou

Using the combined bioelectrochemical and sulfur autotrophic denitrification system for groundwater denitrification

A combined bioelectrochemical and sulfur autotrophic denitrification system (CBSAD) was evaluated to treat a groundwater with nitrate contamination (20.9-22.0mgNO(3)(-)-N/L). The reactor was operated continuously for several months with groundwater to maximize treatment efficiency under different hydraulic retention times (HRT) and electric currents. The denitrification rate of sulfur autotrophic part followed a half-order kinetics model. Moreover, the removal efficiency of bioelectrochemical part depended on the electric current. The reactor could be operated efficiently at the HRT ranged from 4.2 to 2.1h (corresponding nitrogen volume-loading rates varied from 0.12 to 0.24 kg N/m(3)d; and optimum current ranged from 30 to 1000 mA), and the NO(3)(-)-N removal rate ranged from 95% to 100% without NO(3)(-)-N accumulation. The pH of effluent was satisfactorily adjusted by bioelectrochemical part, and the sulfate concentration of effluent was lower than 250 mg/L, meeting the drinking water standard of China EPA.

Electro-photocatalytic degradation of acid orange II using a novel TiO2/ACF photoanode.

A novel photoanode was prepared by immobilizing TiO(2) film onto activated carbon fibers (TiO(2)/ACF) using liquid phase deposition (LPD) to study the electro-photocatalytic (EPC) degradation of organic compounds exemplified by an azo-dye, namely, Acid Orange II (AOII). Results demonstrated that by applying a 0.5 V bias (vs. SCE) across the TiO(2)/ACF electrode, the AOII degradation rate was increased significantly compared to that of photocatalytic (PC) oxidation. The application of an electric field promotes the separation of photogenerated electrons and holes as confirmed by electrochemical impedance spectroscopy (EIS) measurements. The structural and surface morphology of the TiO(2)/ACF electrode was characterized by field emission scanning electron microscopy (FE-SEM) and X-ray diffraction (XRD). SEM images showed that TiO(2) was deposited on almost every carbon fiber with an average thickness of about 200 nm with the inner space between neighboring fibers being maintained unfilled. The morphological features of the photo-anode facilitated the passage of solution as well as UV light through the felt-form electrode and created a three-dimensional environment favorable to EPC oxidation. Both the large outer surface area of the 3D electrode and the good organic adsorption capacity of the ACF support promoted high contact efficiency between AOII and TiO(2) surface. Anatase was the major crystalline TiO(2) deposited. UV-vis spectrophotometry, TOC (total organic carbon) analysis, and HPLC technique were used to monitor the concentration change of AOII and intermediates as to gain insight into the EPC degradation of AOII using the TiO(2)/ACF electrode.

Effects of amino acids on microcystin production of the Microcystis aeruginosa

A Microcystis aeruginosa which produced high content of microcystin-LR (MC-LR) but no microcystin-RR (MC-RR) was isolated from Dianchi Lake in China. In the molecular structure of MC-LR, glutamic acid, aspartic acid, leucine, alanine and arginine are the constitutional components which are abundant in natural water. In this paper, effects of six amino acids at their natural concentrations on the growth of the M. aeruginosa and the microcystin (MC) production were studied in batch culture. M. aeruginosa could assimilate alanine, leucine and arginine as sole nitrogen sources for growth and MC production. However, glutamic acid, aspartic acid and lysine could not be assimilated quickly, although they could pass the cell membrane and enter into the cell rapidly. Our experiment demonstrated that the possible reason of such phenomenon was that different amino acids had different effects on the process of metabolism through the free dissolved amino acids within the cells.

Role of the Mg/Al atomic ratio in hydrotalcite-supported Pd/Sn catalysts for nitrate adsorption and hydrogenation reduction.

Hydrotalcite-supported Pd/Sn catalysts with different Mg/Al atomic ratios (2, 3, 4, and 5) for nitrate adsorption and hydrogenation reduction were successfully synthesized by a coprecipitation method. The results showed that different atomic ratios of Mg/Al resulted in different interlayer spacings and zeta-potentials of the catalysts, which thus influenced its adsorption capacity. With the increase of Mg/Al atomic ratio, the interlayer spacing rose and zeta-potential decreased. The adsorption properties of the catalysts were mainly affected by interlayer spacing when Mg/Al atomic ratios increased from 2 to 4. However, when Mg/Al atomic ratios further increased from 4 to 5, there was a negative impact on the adsorption properties of zeta-potential. Also, the adsorption capacity of the catalysts for nitrate followed the order: Mg/Al=2<Mg/Al=3<Mg/Al=5<Mg/Al=4. In the catalytic reduction process, the adsorbed nitrates were further reduced to nitrites that remained in the same position in catalysts, but some of superabundant nitrites were released into water as primary and unstable products. The concentration of released nitrites was in the reverse order of the adsorption capacity. The catalytic selectivity and activity of the catalysts for nitrate reduction had the same sequence as its adsorption capacity.

Electrochemical incineration of dimethyl phthalate by anodic oxidation with boron-doped diamond electrode

The anodic oxidation of aqueous solutions containing dimethyl phthalate (DMP) up to 125 mg/L with sodium sulfate (Na2SO4) as supporting electrolyte within the pH range 2.0-10.0 was studied using a one-compartment batch reactor employing a boron-doped diamond (BDD) as anode. Electrolyses were carried out at constant current density (1.5-4.5 mA/cm2). Complete mineralization was always achieved owing to the great concentration of hydroxyl radical (*OH) generated at the BDD surface. The effects of pH, apparent current density and initial DMP concentration on the degradation rate of DMP, the specific charge required for its total mineralization and mineralization current efficiency were investigated systematically. The mineralization rate of DMP was found to be pH-independent and to increase with increasing applied current density. Results indicated that this electrochemical process was subjected, at least partially, to the mass transfer of organics onto the BDD surface. Kinetic analysis of the temporal change of DMP concentration during electrolysis determined by High Performance Liquid Chromatography (HPLC) revealed that DMP decay under all tested conditions followed a pseudo first-order reaction. Aromatic intermediates and generated carboxylic acids were identified by Gas Chromatography-Mass Spectrometry (GC-MS) and a general pathway for the electrochemical incineration of DMP on BDD was proposed.

Relationship of energy charge and toxin content of Microcystis aeruginosa in nitrogen-limited or phosphorous-limited cultures.

Effects of nitrogen-limitation and phosphorus-limitation on microcystin (MC) content and energy charge (EC) of the Microcystis aeruginosa were investigated in batch cultures and semi-continuous cultures. In batch cultures, nitrogen-limitation retarded the MC synthesis and phosphorus-limitation had little effects on MC production. The EC remained constant in nitrogen-limited cultures, while it decreased largely when phosphorus was extinct in phosphorus-limited culture. In the semi-continuous cultures, MC production in nitrogen- and phosphorus-limited cultures increased with the increase of dilution rate; however, MC content in phosphorus-limited cultures was more than that in nitrogen-limited cultures. The EC in nitrogen-limited cultures remained constant and in phosphorus-limited cultures increased with the increase of dilution rate. In phosphorus-limited semi-continuous cultures, a direct relationship between EC and MC content was demonstrated. No correlation was observed in nitrogen-limited semi-continuous cultures. Based on the above analysis, a mechanism of nitrogen and phosphorus effect on the MC synthesis was suggested, that the MC synthesis was determined by the combination of necessary enzymes and precursors and EC.

Combination of electroreduction with biosorption for enhancement for removal of hexavalent chromium

Hexavalent chromium is one of the most toxic heavy metals in aqueous solutions. It has been well documented that the brown seaweed can be used as a promising biosorbent for the sequestration of this heavy metal from wastewater. However, the uptake of Cr(VI) is reportedly a rather slower process; the sorption equilibrium can only be established after a few days, much slower than a few hours for the trivalent chromium ion. In this study, we developed a novel technology of electrochemically assisted biosorption (ECAB) system for the enhancement of the treatment efficiency. It was found through our study that the removal efficiencies of Cr(VI) and total chromium were greatly enhanced by 48.1% and 51.3%, respectively, with the application of -1.0 V in the ECAB system. The conversion of Cr(III) due to the electroreduction of Cr(VI) and the higher pH due to the cathodic H(2) evolution created a favorable condition for the uptake of chromium onto the modified seaweed (MSW). The reduction and adsorption of Cr(VI) by MSW was proved to play a minor role in the removal. Both direct electroreduction and indirect electroreduction by atomic H* contributed to the reduction of Cr(VI).