Enhanced 1,2-dichloroethane removal using g-C3N4/Blue TiO2 nanotube array photoanode in microbial photoelectrochemical cells.

The compound 1,2-dichloroethane (1,2-DCA), a persistent and ubiquitous pollutant, is often found in groundwater and can strongly affect the ecological environment. However, the extreme bio-impedance of C-Cl bonds means that a high energy input is needed to drive biological dechlorination. Biotechnology techniques based on microbial photoelectrochemical cell (MPEC) could potentially convert solar energy into electricity and significantly reduce the external energy inputs currently needed to treat 1,2-DCA. However, low electricity-generating efficiency at the anode and sluggish bioreaction kinetics at the cathode limit the application of MPEC. In this study, a g-C3N4/Blue TiO2-NTA photoanode was fabricated and incorporated into an MPEC for 1,2-DCA removal. Optimal performance was achieved when Blue TiO2 nanotube arrays (Blue TiO2-NTA) were loaded with graphitic carbon nitride (g-C3N4) 10 times. The photocurrent density of the g-C3N4/Blue TiO2-NTA composite electrode was 2.48-fold higher than that of the pure Blue TiO2-NTA electrode under light irradiation. Furthermore, the MPEC equipped with g-C3N4/Blue TiO2-NTA improved 1,2-DCA removal efficiency by 45.21% compared to the Blue TiO2-NTA alone, which is comparable to that of a microbial electrolysis cell. In the modified MPEC, the current efficiency reached 69.07% when the light intensity was 150 mW cm-2 and the 1,2-DCA concentration was 4.4 mM. The excellent performance of the novel MPEC was attributed to the efficient direct electron transfer process and the abundant dechlorinators and electroactive bacteria. These results provide a sustainable and cost-effective strategy to improve 1,2-DCA treatment using a biocathode driven by a photoanode.

Boosting o-xylene removal and power generation in an airlift microbial fuel cell system.

Microbial fuel cells (MFCs) are widely acknowledged to be a promising eco-friendly abatement technology of pollutants, and are capable of generating electricity. However, the poor mass transfer and reaction rate in MFCs significantly decrease their treatment capacity for contaminants, especially hydrophobic substances. The present work developed a novel MFC integrated with an airlift (ALR) reactor using a polypyrrole modified anode to promote the bioaccessibility of gaseous o-xylene and attachment of microorganisms. The results indicated that the established ALR-MFC system showed excellent elimination capability, with removal efficiency exceeding 84% even at high o-xylene concentration (1600 mg m-3). The maximum output voltage of 0.549 V and power density of 13.16 mW m-2 obtained by the Monod-type model were approximately twice and sixfold higher than that of a conventional MFC, respectively. According to the microbial community analysis, the superior performances of the ALR-MFC in terms of o-xylene removal and power generation were mainly ascribed to the enrichment of degrader (i.e. Shinella) and electrochemical active bacteria (i.e. Proteiniphilum). Moreover, the electricity generation of the ALR-MFC did not decrease at a high O2 concentration, as O2 was conducive to o-xylene degradation and electron release. The supplication of an external carbon source such as sodium acetate (NaAc) was conducive to increasing output voltage and coulombic efficiency. The electrochemical analysis revealed that released electrons can be transmitted with the action of NADH dehydrogenase to OmcZ, OmcS, and OmcA outer membrane proteins via a direct or indirect pathway, and ended up transferring to the anode directly.

BiOI-SnO2 Heterojunction Design to Boost Visible-Light-Driven Photocatalytic NO Purification.

The efficient, stable, and selective photocatalytic conversion of nitric oxide (NO) into harmless products such as nitrate (NO3-) is greatly desired but remains an enormous challenge. In this work, a series of BiOI/SnO2 heterojunctions (denoted as X%B-S, where X% is the mass portion of BiOI compared with the mass of SnO2) were synthesized for the efficient transformation of NO into harmless NO3-. The best performance was achieved by the 30%B-S catalyst, whose NO removal efficiency was 96.3% and 47.2% higher than that of 15%B-S and 75%B-S, respectively. Moreover, 30%B-S also exhibited good stability and recyclability. This enhanced performance was mainly caused by the heterojunction structure, which facilitated charge transport and electron-hole separation. Under visible light irradiation, the electrons gathered in SnO2 transformed O2 to ·O2- and ·OH, while the holes generated in BiOI oxidized H2O to produce ·OH. The abundantly generated ·OH, ·O2-, and 1O2 species effectively converted NO to NO- and NO2-, thus promoting the oxidation of NO to NO3-. Overall, the heterojunction formation between p-type BiOI and n-type SnO2 significantly reduced the recombination of photo-induced electron-hole pairs and promoted the photocatalytic activity. This work reveals the critical role of heterojunctions during photocatalytic degradation and provides some insight into NO removal.

External potential regulated biocathode for enhanced removal of gaseous chlorobenzene in bioelectrchemical system.

Microbial electrolysis cell (MEC) with a biocathode could provide extra reaction driving force for gaseous chlorobenzene (CB) removal. In this work, external potentials (-0.1 to -0.7 V vs. SHE) were applied to regulate the biocathodic activity. Results showed -0.3 V was the optimum potential, while the removal efficiency, dechlorination efficiency and Coulombic efficiency achieved 94%, 65%, and 89%, respectively. Electrochemical stimulation enriched dechlorination microorganisms (Achromobacter and Gordonia), and significantly improved CB mineralization efficiency, which was twice higher than that without additional potential at 300 mg m-3 inlet concentration. Furthermore, electron transfer between biocathode and microorganisms was mainly through direct electron transfer (DET). A new integrated redox pathway for CB anaerobic degradation was proposed, in which CB was sequentially converted into 2-chlorophenol and 3-chlorocatechol, then dechlorinated to catechol, and finally mineralized into CO2. Overall, this work provided an insight into gaseous CB bioelectrochemical degradation through the potential regulation.

Performance and mechanism of carbon dioxide fixation by a newly isolated chemoautotrophic strain Paracoccus denitrificans PJ-1.

CO2 is regarded as a major contributor to the global warming. CO2 utilization is promising to reduce the CO2 emissions. Currently, the biofixation of CO2 using chemoautotrophs has markedly gain interest in CO2 utilization. In this study, a newly isolated chemoautotroph, Paracoccus denitrificans PJ-1, was used for the biofixation of CO2 under anaerobic condition. Experimental results revealed that Paracoccus denitrificans PJ-1 achieved a high carbon fixation rate (13.25 mg·L-1·h-1) which was ∼10 times faster than the previous reported chemotrophic bacteria using thiosulfate as electron donor. The best CO2 fixation activity of Paracoccus denitrificans PJ-1 was achieved at the pH value of 9.0 and CO2 concentration of 20 vol%. Meanwhile, a high CO2 fixation yield of 106.03 mg·L-1 was reached. The presence of oxygen was adverse to the biofixation, indicating that strain PJ-1 was more suitable for CO2 fixation in anaerobic environments. Carbon mass balance analysis revealed that the carbon from CO2 was mainly fixed into the extracellular organic carbon rather than the biomass. GC-MS analysis and cbbL gene test revealed that Paracoccus denitrificans PJ-1 fixed CO2 through the Calvin-Benson-Bassham cycle and mainly converted CO2 to oxalic acid and succinic acid. Overall, the excellent CO2 fixation capacity of Paracoccus denitrificans PJ-1 suggests that it had potential for CO2 utilization.

Superior performance and mechanism of chlorobenzene degradation by a novel bacterium.

A newly isolated strain was identified as Ochrobactrum sp. by 16S rRNA sequence analysis and named as ZJUTCB-1. The strain was able to degrade mono-chlorobenzene (CB) as the sole carbon and energy source under aerobic conditions. This study is the first to report the degradation of CB by the genus Ochrobactrum. The degradation rate of CB reached 170.9 µmol L-1 h-1, which is at least 6 times higher than the previously reported data. The strain can efficiently degrade CB under a rang of temperatures (30-40 °C) and pH (6.0-7.0) with optimum at 40 °C and pH 7.0. Salt concentration higher than 0.05 mol L-1 remarkably reduced the biodegradation capability. Moreover, true oxic condition was not an essential element for biodegradation given that the CB degradation rate of 210.4 µmol L-1 h-1 was obtained under microaerobic condition. Based on the Haldane kinetic model, the maximum specific growth rate was 0.895 h-1, which is the highest in ever described CB-degrading strains. According to GC-MS analysis and enzymatic assay, CB was degraded via the meta-cleavage pathway by using 2,3-dioxygenase and 2-chlorophenol as the main intermediates, producing CO2 and Cl- as the final products. The great performance of CB degradation by Ochrobactrum sp. ZJUTCB-1 provided an alternative for development of more effective and reliable biotreatment process.