Enhanced biodegradation of perfluorooctanoic acid in a dual biocatalyzed microbial electrosynthesis system.

The toxic perfluorooctanoic acid (PFOA) is widely spread in terrestrial and aquatic habitats owing to its resistance to conventional degradation processes. Advanced techniques to degrade PFOA requires drastic conditions with high energy cost. In this study, we investigated PFOA biodegradation in a simple dual biocatalyzed microbial electrosynthesis system (MES). Different PFOA loadings (1, 5, and 10 ppm) were tested and a biodegradation of 91% was observed within 120 h. Propionate production improved and short-carbon-chain PFOA intermediates were detected, which confirmed PFOA biodegradation. However, the current density decreased, indicating an inhibitory effect of PFOA. High-throughput biofilm analysis revealed that PFOA regulated the microbial flora. Microbial community analysis showed enrichment of the more resilient and PFOA adaptive microbes, including Methanosarcina and Petrimonas. Our study promotes the potential use of dual biocatalyzed MES system as an environment-friendly and inexpensive method to remediate PFOA and provides a new direction for bioremediation research.

Enhanced bio-electrochemical performance of microbially catalysed anode and cathode in a microbial electrosynthesis system.

Most bio-electrochemical systems (BESs) use biotic/abiotic electrode combinations, with platinum-based abiotic electrodes being the most common. However, the non-renewability, cost, and poisonous nature of such electrode systems based on noble metals are major bottlenecks in BES commercialisation. Microbial electrosynthesis (MES), which is a sustainable energy platform that simultaneously treats wastewater and produces chemical commodities, also faces the same problem. In this study, a dual bio-catalysed MES system with a biotic anode and cathode (MES-D) was tested and compared with a biotic cathode/abiotic anode system (MES-S). Different bio-electrochemical tests revealed improved BES performance in MES-D, with a 3.9-fold improvement in current density compared to that of MES-S. Volatile fatty acid (VFA) generation also increased 3.2-, 4.1-, and 1.8-fold in MES-D compared with that in MES-S for acetate, propionate, and butyrate, respectively. The improved performance of MES-D could be attributed to the microbial metabolism at the bioanode, which generated additional electrons, as well as accumulative VFA production by both the bioanode and biocathode chambers. Microbial community analysis revealed the enrichment of electroactive bacteria such as Proteobacteria (60%), Bacteroidetes (67%), and Firmicutes + Proteobacteria + Bacteroidetes (75%) on the MES-S cathode and MES-D cathode and anode, respectively. These results signify the potential of combined bioanode/biocathode BESs such as MES for application in improving energy and chemical commodity production.

Electrocatalytic oxidation of antidiabetic drug metformin adsorbed on intercalated MXene.

Two-dimensional (2D) Ti3C2Tx transition metal carbide (MXene) nanosheets intercalated with sodium ions (SI-Ti3C2Tx MXene) were used in the adsorption and electrochemical regeneration process for removal of the antidiabetic drug metformin (MF) as a model emerging pollutant. After MF adsorption, SI-Ti3C2Tx MXene oxidized the MF on its surface through its electrocatalytic activity at very low current density and cell potential. For complete oxidation the optimum parameters were 0.525 C g-1, 0.005 mA cm-2, and pH 6 in absence of NaCl or 26.25 C g-1 and 0.5 mA cm-2 in the presence of 2.5 w/v% NaCl. The overall regeneration of SI-Ti3C2Tx is governed by a combined mechanism, i.e., desorption followed by degradation. The degradation mechanism, such as direct electron transfer or indirect oxidation, depends on the applied operating conditions. Thus, the investigation suggests that these 2D sheets are good nanoadsorbents as well as good electrocatalysts and proves their usefulness in practical water-treatment applications.

Development of a three-dimensional macroporous sponge biocathode coated with carbon nanotube-MXene composite for high-performance microbial electrosynthesis systems.

Microbial electrosynthesis (MES) is a renewable energy platform capable of reducing the carbon footprint by converting carbon dioxide/bicarbonate to useful chemical commodities. However, the development of feasible electrode structures, inefficient current densities, and the production of unfavorable electrosynthesis products remain a major challenge. To this end, a three-dimensional (3D) macroporous sponge coated with a carbon nanotube/MXene composite (CNT-MXene@Sponge) was evaluated as an MES cathode. The macroporous scaffold, together with intrinsic electrical conductivity, enhanced the charge transfer efficiency and selective microbial enrichment characteristics of the CNT-MXene@Sponge cathode resulted in an average current density of -324 mA m-2, which was substantially higher than that of the uncoated (-100 mA m-2), CNT (-141 mA m-2), and MXene (-214 mA m-2) coated sponge electrode. The uniform 3D structure and abundant active sites of the coated material facilitated mass diffusion and microbial growth, which produced 1.5 orders of magnitude higher butyrate than the uncoated sponge. The high-throughput sequencing results showed the selective enrichment of electrogenic and butyrate-producing phylum, Firmicutes. These results suggest that the MES performance could be enhanced using the collective features of large-pore network structure, such as better conductivity, improved capacitance, and selective microbial enrichment.

MXene-coated biochar as potential biocathode for improved microbial electrosynthesis system.

Microbial electrosynthesis (MES) holds tremendous large scale energy storage potential. By promoting the bioconversion of carbon dioxide (bicarbonate) into useful chemical commodities, this technique utilizes renewable energy and reduces carbon footprint. However, expensive electrode materials, low current densities, and multiple electrosynthesis products are major challenges to this field. To this end, this study examines a multilayered and conductive MXene structure that was coated on a cost-effective biochar substrate and tested as a MES cathode. These results show this coating yielded improved electrical conductivity, increased charge transfer efficiency, and selective microbial enrichment characteristics, resulting in a 2.3-fold increase in cathodic current production in comparison to the uncoated biochar. Moreover, an increase in active sites improved mass transfer and microbial growth, producing 1.7-fold increase in butyrate in comparison to the uncoated control. Considering that electrode attached microbial communities play a major role in final products, microbial community analyses was completed, suggesting that selective microbial enrichment was promoted as Firmicutes (66%), Proteobacteria (13%), and Bacteroidetes (12%) (i.e., exoelectrogenic and butyrate producing phyla) which were dominant in the MXene-coated biochar biofilm. These results show that biochar modification is an effective technique for achieving selective products through MES.

Enhanced product selectivity in the microbial electrosynthesis of butyrate using a nickel ferrite-coated biocathode.

Microbial electrosynthesis (MES) is a potential sustainable biotechnology for the efficient conversion of carbon dioxide/bicarbonate into useful chemical commodities. To date, acetate has been the main MES product; selective electrosynthesis to produce other multi-carbon molecules, which have a higher commercial value, remains a major challenge. In this study, the conventional carbon felt (CF) was modified with inexpensive nickel ferrite (NiFe2O4@CF) to realize enhanced butyrate production owing to the advantages of improved electrical conductivity, charge transfer efficiency, and microbial-electrode interactions with the selective microbial enrichment. Experimental results show that the modified electrode yielded 1.2 times the butyrate production and 2.7 times the cathodic current production of the CF cathode; product selectivity was greatly improved (from 37% to 95%) in comparison with CF. Microbial community analyses suggest that selective microbial enrichment was promoted as Proteobacteria and Thermotogae (butyrate-producing phyla) were dominant in the NiFe2O4@CF biofilm (~78%). These results demonstrate that electrode modification with NiFe2O4 can help realize greater selective carboxylate production with improved MES performance. Hence, this technology is expected to be greatly useful in future reactor designs for scaled-up technologies.

MnCo2O4 coated carbon felt anode for enhanced microbial fuel cell performance.

A highly efficient anode is very crucial for an improved microbial fuel cell (MFC) performance. In this study, a binder-free manganese cobalt oxide (MnCo2O4@CF) anode was synthesized using a conventional carbon felt (CF) by a facile hydrothermal method. A large electrochemically active and rough electrode surface area of MnCo2O4@CF anode improved the substrate fluxes and microbial adhesion/growth. Furthermore, the electrochemical tests on the synthesized anode confirmed the superior bioelectrochemical activity, reduced ion transfer resistance, and excellent capacitance. This resulted in an improved power density (945 mW/m2), which was 3.8 times higher than that of CF anode. The variable valence state, high stability and biocompatibility of MnCo2O4@CF resulted in continuous current density performance for five MFC cycles. High-throughput biofilm analysis revealed the enrichment of electricity producing phylum of Proteobacteria and Bacteroidetes (∼90.0%), which signified that the modified MnCo2O4 anode accelerated the enrichment of electro-active microbes.

Nickel ferrite/MXene-coated carbon felt anodes for enhanced microbial fuel cell performance.

In recent years, the modification of electrode materials for enhancing the power generation of microbial fuel cells (MFCs) has attracted considerable attention. In this study, a conventional carbon felt (CF) electrode was modified by NiFe2O4 (NiFe2O4@CF), MXene (MXene@CF), and NiFe2O4-MXene (NiFe2O4-MXene@CF) using facile dip-and-dry and hydrothermal methods. In these modified CF electrodes, the electrochemical performance considerably improved, while the highest power density (1385 mW/m2), which was 5.6, 2.8, and 1.4 times higher than those of CF, NiFe2O4@CF, and MXene@CF anodes, respectively, was achieved using NiFe2O4-MXene@CF. Furthermore, electrochemical impedance spectroscopy and cyclic voltammetry results confirmed the superior bioelectrochemical activity of a NiFe2O4-MXene@CF anode in a MFC. The improved performance could be attributed to the low charge transfer resistance, high conductivity and number of catalytically active sites of the NiFe2O4-MXene@CF anode. Microbial community analysis demonstrated the relative abundance of electroactive bacteria on a NiFe2O4-MXene@CF anodic biofilm rather than CF, MXene@CF, and NiFe2O4@CF anodes. Therefore, these results suggest that combining the favorable properties of composite materials such as NiFe2O4-MXene@CF anodes can open up new directions for fabricating novel electrodes for renewable energy-related applications.

Investigating the role of anodic potential in the biodegradation of carbamazepine in bioelectrochemical systems.

Anode potential is a critical factor in the biodegradation of organics in bioelectrochemical systems (BESs), but research on these systems with complex recalcitrant co-substrates at set anode potentials is scarce. In this study, carbamazepine (CBZ) biodegradation in a BES was examined over a wide range of set anode potentials (-200 to +600 mV vs Ag/AgCl). Current generation and current densities were improved with the increase in positive anode potentials. However, at a negative potential (-200 mV), current generation was higher as compared to that for +000 and +200 mV. The highest CBZ degradation (84%) and TOC removal efficiency (70%) were achieved at +400 mV. At +600 mV, a decrease in CBZ degradation was observed, which can be attributed to a low number of active bacteria and a poor ability to adapt to high voltage. This study signified that BESs operated at optimum anode potentials could be used for enhancing the biodegradation of complex and recalcitrant contaminants in the environment.

Exfoliation of Titanium Aluminum Carbide (211 MAX Phase) to Form Nanofibers and Two-Dimensional Nanosheets and Their Application in Aqueous-Phase Cadmium Sequestration.

A green approach was adopted to exfoliate a Ti2AlC MAX phase. The exfoliated nanostructures (Alk-Ti2Cfibr and Alk-Ti2Csheet) with exceptional mechanical, thermal, and water stabilites, as well as abundant oxygenated active binding sites, were synthesized via a controlled hydrothermal treatment in an alkaline environment. The successful synthesis of nanofibers and sheetlike nanostructures was inferred with scanning electron microscopy and X-ray diffraction analyses. Field emission scanning electron microscopy, field-emission transmission electron microscopy, Raman spectroscopy, Brunauer-Emmett-Teller surface area, ζ-potential analyses, and X-ray photoelectron spectroscopy were utilized to investigate the material's characteristics and its structural changes after metal ion adsorption. Heavy metal ion adsorption of the synthesized nanostructures was assessed in batch tests based on Cd2+ ion sequestration; the maximum adsorption capacity for Cd2+ was 325.89 mg/g, which is among the highest values reported for similar materials such as graphene oxide and its derivatives. The detailed quantitative investigation confirmed the interaction of hydroxyl groups with Cd2+ ions by electrostatic interactions, adsorption-coupled oxidation, and complex formation. Owing to their unique structure, high porosity, large specific surface area, and oxygenated functional groups, Alk-Ti2Csheet nanosheets were highly time-efficient for Cd2+ removal. Moreover, Alk-Ti2Cfibr and Alk-Ti2Csheet nanostructures were tested for simulated groundwater, showing that synthesized nanostructures were capable for removing Cd2+ ions at the ppb level. The results obtained from this study suggested that nanostructures synthesized using this route could provide a new approach to prepare and exfoliate additional MAX phases for the removal of heavy metal ions and other pollutants in the environment.