Hybrid microbial electrolytic/UV system for highly efficient organic pollutants removal.

This study for the first time proposed an efficient microbial electrolyte/UV system for Methyl Orange decomposition. With an external applied voltage of 0.2 V and cathode aeration of 20 mL/min, H2O2 could be in-situ generated from two-electron reduction of oxygen in cathode, reaching to 8.1 mg/L in 2 hr and continued to increase. The pollutant removal efficiency of approximate 94.7% was achieved at initial neutral pH, with the activation of •OH in the presence of UV illumination. Although the nature of its guiding principles remain on the vista of practical exploration, this proof-of-concept study provides an alternative operation pattern of solar-microbial hybrid technology for future wastewater treatment from a basic but multidisciplinary view.

CO2 sequestration in microbial electrolytic cell-anaerobic digestion system combined with mineral carbonation for sludge hydrolysate treatment.

The combination of microbial electrolytic cells and anaerobic digestion (MEC-AD) became an efficient method to improve CO2 capture for waste sludge treatment. By adding CaCl2 and wollastonite, the CO2 sequestration effect with mineral carbonation under 0 V and 0.8 V was studied. The results showed that applied voltage could increase dissolved chemical oxygen demand (SCOD) degradation efficiency and biogas yield effectively. In addition, wollastonite and CaCl2 exhibited different CO2 sequestration performances due to different Ca2+ release characteristics. Wollastonite appeared to have a better CO2 sequestration effect and provided a wide margin of pH change, but CaCl2 released Ca2+ directly and decreased the pH of the MEC-AD system. The results showed methane yield reached 137.31 and 163.50 mL/g SCOD degraded and CO2 content of biogas is only 12.40 % and 2.22 % under 0.8 V with CaCl2 and wollastonite addition, respectively. Finally, the contribution of chemical CO2 sequestration by mineral carbonation and biological CO2 sequestration by hydrogenotrophic methanogenesis was clarified with CaCl2 addition. The chemical and biological CO2 sequestration percentages were 46.79 % and 53.21 % under 0.8 V, respectively. With the increased applied voltage, the contribution of chemical CO2 sequestration rose accordingly. The findings in this study are of great significance for further comprehending the mechanism of calcium addition on CO2 sequestration in the MEC-AD system and providing guidance for the later engineering application.

Degradation of sulfamethazine by microbial electrolysis cell with nickel-cobalt co-modified biocathode.

In this study, nickel-cobalt co-modified stainless steel mesh (Ni-Co@SSM) was prepared and used as the biocathode in microbial electrolysis cell (MEC) for sulfamethazine (SMT) degradation. The optimal electrochemical performance of the Ni-Co@SSM was obtained at the electrodeposition time of 600 s, electrodeposition current density of 20 mA cm-2, and nickel-cobalt molar ratio of 1:2. The removal of SMT in MEC with the Ni-Co@SSM biocathode (MEC-Ni-Co@SSM) was 82%, which increased by 30% compared with the conventional anaerobic reactor. Thirteen intermediates were identified and the potential degradation pathways of SMT were proposed. Proteobacteria, Firmicutes, Patescibacteria, Chloroflexi, Bacteroidetes, and Euryarchaeota are the dominant bacteria at the phylum level in the MEC-Ni-Co@SSM, which are responsible for SMT metabolism. Due to the electrical stimulation, there was an increase in the abundance of the metabolic function and the genetic information processing. This work provides valuable insight into utilizing MECs for effective treatment of antibiotic-containing wastewater.

Performance and mechanism of azo dyes degradation and greenhouse gases reduction in single-chamber electroactive constructed wetland system.

A single-chamber microbial fuel cell-microbial electrolytic cell with a novel constructed wetland system was proposed for synergistic degradation of congo red and reduction in emissions of greenhouse gases. The closed-circuit system showed higher chemical oxygen demand and congo red removal efficiencies by 98 % and 96 % on average, respectively, than traditional constructed wetland. It could also significantly reduce the emissions of CH4 and N2O (about 52 % CO2-equivalents) by increasing the electron transfer. Microbial community analysis demonstrated that the progressive enrichment of dye-degrading microorganisms (Comamonas), electroactive bacteria (Tolumonas, Trichococcus) and denitrifying microorganisms (Dechloromonas) promoted pollutant removal and electron transfer. Based on gene abundance of xenobiotics biodegradation, the congo red biodegradation pathway was described as congo red â†’ naphthalene and alcohols â†’ CO2 and H2O. In summary, the single-chamber closed-circuit system could significantly improve the degradation of congo red and reduce the emissions of greenhouse gases by influencing electron transfer and microbial activity.

Magnetite-enhanced bioelectrochemical stimulation for biodegradation and biomethane production of waste activated sludge.

Microbial electrolytic cell (MEC) and magnetite (M) have shown excellent performance in promoting anaerobic digestion (AD) of biowastes. In this study, four types of anaerobic systems (i.e. single AD, M-AD, MEC-AD, and M-MEC-AD) were developed to comprehensively investigate the potential effects of magnetite-enhanced bioelectrochemical stimulation on the biodegradation of waste activated sludge (WAS) and methane (CH4) production. Results showed that M-MEC-AD system produced the highest cumulative CH4 yield, 9.4% higher than that observed in MEC-AD system. Bioelectrochemical stimulation enriched electroactive Geobacter, and classical methanogens (Methanosaeta and Methanobacterium), and the proliferation was further promoted when coupling with magnetite. The relative abundance of Geobacter (6.9%), Methanosaeta (0.3%), and Methanobacterium (12.6%) in M-MEC-AD system was about 10.8, 1.2, and 1.2 times of MEC-AD system, respectively. The integration of magnetite could serve as the conductive materials, and promote inherent indirect electron transfer (IET) and emerging direct electron transfer (DET) between methanogens and fermentative bacteria, building a more energy-efficient route for interspecies electron transfer and methane productivity. This study demonstrated the positive promotion of the coupled bioelectrochemical regulation and magnetite on organic biodegradation, process stability and CH4 productivity, providing some references for the integrated technology in sludge treatment and bioenergy recovery.

A Review on Microbial Electrocatalysis Systems Coupled with Membrane Bioreactor to Improve Wastewater Treatment.

Microbial electrocatalysis is an electro reaction that uses microorganisms as a biocatalyst, mainly including microbial electrolytic cells (MEC) and microbial fuel cells (MFC), which has been used for wastewater treatment. However, the low processing efficiency is the main drawback for its practical application and the additional energy input of MEC system results in high costs. Recently, MFC/MEC coupled with other treatment processes, especially membrane bioreactors (MBR), has been used for high efficiency and low-cost wastewater treatment. In these systems, the wastewater treatment efficiency can be improved after two units are operated and the membrane fouling of MBR can also be alleviated by the electric energy that was generated in the MFC. In addition, the power output of MFC can also reduce the energy consumption of microbial electrocatalysis systems. This review summarizes the recent studies about microbial electrocatalysis systems coupled with MBR, describing the combination types and microorganism distribution, the advantages and limitations of the systems, and also addresses several suggestions for the future development and practical applications.