Nickel-iron-driven heterogenous bio-electro-fenton process for the degradation of methylparaben.

Discharge of emerging contaminants such as parabens in natural water bodies is a grievous concern. Among parabens, methylparaben (MP) is most prevalent due to its extensive usage in personal care and food products and has been purported to trigger hormonal-related diseases. In this regard, the bio-electro-Fenton (BEF) process garners attention for remediating refractory compounds because of its ability to generate in situ hydroxyl radicals (•OH) utilising the energy harvested from electroactive microorganisms. In the present investigation, a Ni-Fe-driven heterogenous BEF system (BEF-MFC) was used to degrade MP from different matrices. At neutral catholyte pH, 99.54 ± 0.22% of MP was removed from an initial concentration of 10 mg/L in 240 min of retention time with an estimated treatment cost of about 1.01 $/m3. The removal rate ameliorated when the catholyte pH was dropped to 3.0 and by imposing an external voltage of 0.5 V, requiring just 120 min to achieve comparable MP removal efficiencies. However, catalyst leaching was higher at acidic pH (leaching of Fe ions = 0.44 mg/L and Ni ions = 0.06 mg/L) and applying external voltage increased the treatment cost slightly to 1.08 $/m3. Further, treatment of 10 mg/L MP-spiked real wastewater at pH of 7.0 with the BEF-MFC attained 85.70 ± 3.30% and 56.50 ± 1.70% reduction in MP and total organic carbon, respectively, in 240 min. In addition, a maximum power density of 205.90 ± 2.27 mW/cm2 was harvested in the BEF-MFC; thus, portraying the dual benefit of Ni-Fe heterogeneous catalyst. Even though, Ni-Fe performed reasonably well as Fenton-cum-cathode catalyst, future endeavours should be poised to fine-tune catalysts to accelerate H2O2 and •OH generation, which will reinforce the scalability of this system.

Graphene and biochar-based cathode catalysts for microbial fuel cell: Performance evaluation, economic comparison, environmental and future perspectives.

Microbial fuel cells (MFCs) have been the prime focus of research in recent years because of their distinctive feature of concomitantly treating and producing electricity from wastewater. Nevertheless, the electrical performance of MFCs is hindered by a protracted oxygen reduction reaction (ORR), and often a catalyst is required to boost the cathodic reactions. Conventional transition metals-based catalysts are expensive and infeasible for field-scale usage. In this regard, carbon-based electrocatalysts like waste-derived biochar and graphene are used to enhance the commercialisation prospects of MFC technology. These carbon-catalysts possess unique properties like superior electrocatalytic activity, higher surface area, and high porosity conducive to ORR. Theoretically, graphene-based cathode catalysts yield superior results than a biochar-derived catalyst, though at a higher cost. In contrast, the synthesis of waste-extracted biochar is economical; however, its ability to catalyse ORR is debatable. Therefore, this review aims to make a side-by-side techno-economic assessment of biochar and graphene-based cathode catalyst used in MFC to predict the relative performance and typical cost of power recovery. Additionally, the life cycle analysis of the graphene and biochar-based materials has been briefly discussed to comprehend the associated environmental impacts and overall sustainability of these carbo-catalysts.

Waste-derived iron catalyzed bio-electro-Fenton process for the cathodic degradation of surfactants.

The application of waste-derived iron for reuse in wastewater treatment is an effective way of utilizing waste and attaining sustainability in the overall process. In the present investigation, bio-electro-Fenton process was initiated for the cathodic degradation of surfactants using waste-iron catalyzed MFC (WFe-MFC). The waste-iron was derived from spent tonner ink using calcination at 600 °C. Three surfactants namely, sodium dodecyl sulphate (SDS), cetyltrimethylammonium bromide, and Triton x-100 were selected as target pollutants. The effect of experimental factors like application of catalyst, contact time, external resistance, and anodic substrate concentration on the SDS degradation was investigated. At a neutral pH, the cathodic surfactants removal efficiency in WFe-MFC was above 85% in a contact time of 180 min with the initial surfactant concentration of ∼20 mg L-1 and external resistance of 100 Ω. The long-term operation using secondary treated real wastewater with unchanged cathode proved that the catalyst was still active to produce effluent SDS concentration of less than 1 mg L-1 in 4 h of contact time after 16 cycles. In a way, the present investigation suggests a potential application for spent tonner ink in the form of Fenton catalyst for wastewater treatment via bio-electro-Fenton MFC.

Microbial fuel cell coupled Fenton oxidation for the cathodic degradation of emerging contaminants from wastewater: Applications and challenges.

Urbanization and industrialization have resulted in the escalation of the occurrence of emerging contaminants (EC) in the wastewater and ultimately to the receiving water bodies due to their bio-refractory nature. The presence of ECs in the water bodies adversely affects all three domains of life, viz. bacteria, archaea and eukaryotes, and eventually the ecosystem. Fenton oxidation is one of the most suitable method that is capable of degrading a variety of ECs by employing a strong oxidizing agent in the form of •OH. The coupling of Fenton oxidation with microbial fuel cell (MFC) offers benefits, such as low-cost, minimal requirement of external energy, and in-situ generation of oxidizing agents. The resulting system, termed as bio-electro-Fenton MFC (BEF-MFC), is capable of degrading the ECs in the cathodic chamber, while harvesting bioelectricity and simultaneously removing oxidizable organic matter from wastewater in the anodic chamber. This review discusses the applications of BEF-MFC for the treatment of dyes, pharmaceuticals, pesticides, and real complex wastewaters. Additionally, the effect of operating conditions on the performance of BEF-MFC are elaborated and emphasis is also given on possible future direction of research that can be adopted in BEF-MFC in the purview of up-scaling.

A novel bio-electro-Fenton process for eliminating sodium dodecyl sulphate from wastewater using dual chamber microbial fuel cell.

The frequent occurrence of surfactants in urban wastewaters represents a multifaceted environmental concern. In this investigation, bio-electro-Fenton-microbial fuel cell (BEF-MFC) was developed for the degradation of sodium dodecyl sulphate (SDS) from wastewater. The synthesised cathode catalyst (powdered activated carbon and iron oxide) facilitated the Fenton reaction in the cathodic chamber of the MFC, concurrently generating a maximum power density of 105.67 mW m-2. The overall performance of the BEF-MFC for SDS removal and power generation excelled the control MFC (C-MFC) having carbon black coated cathode under similar operating conditions. Although, the rate of SDS degradation was favourable in acidic pH, under neutral pH, 70.8 ± 6.4% of SDS degradation was achieved in 120 min in BEF-MFC. A comparison of environmental impacts of BEF-MFC with up-flow MFC and electrochemical oxidation using life cycle assessment tool suggests that BEF-MFC can be one of the promising technologies for the tertiary treatment of wastewater.

Waste-derived biochar: Applications and future perspective in microbial fuel cells.

Application of microbial fuel cell (MFC) is coming to the forefront as a dual-purpose system for wastewater treatment and energy recovery. Future research should emphasize on developing low-cost field-scale MFCs for removal of organic matter, nutrients, xenobiotic and recalcitrant compounds from wastewaters and powering low energy devices. For achieving this, low-cost electrodes, low-cost yet efficient cathode catalysts and proton exchange membrane (PEM) should be developed from waste-based resources to salvage the waste-derived material as much as possible, thereby reducing the fabrication cost of this device. Biochar is one such low-cost material, which has wide range of applications. This review discusses different applications of biochar in MFC, viz. in the form of standalone electrodes, electrocatalyst and material for PEM in light of different characteristics of biochar. Further emphasis is given on the future direction of research for implementation of biochar-based PEMs and electrodes in field-scale MFCs.

Surfactant removal from wastewater using photo-cathode microbial fuel cell and laterite-based hybrid treatment system.

Sodium dodecyl sulfate (SDS) is a widely used anionic surfactant, which finds its way to the receiving water body due to the incapability of conventional wastewater treatment systems to completely remove it. A hybrid treatment system consisting of upflow microbial fuel cell (MFC) with titanium dioxide (TiO2) as a photocathode catalyst was developed for treating synthetic wastewater spiked with SDS (10.00 ± 0.46 mg L-1). Effluent from anodic chamber of MFC was passed through raw laterite soil filter followed by the photo-cathodic chamber with TiO2-coated cathode irradiated with the UV spectrum. This hybrid system was operated under varying hydraulic retention time (HRT) in anodic chamber of MFC. The SDS removal efficiency of more than 96% along with organic matter removal efficiency of more than 71% was obtained by this hybrid system at different HRTs. The MFC having cathode coated with TiO2 could generate a maximum power density of 0.73 W m-3 and 0.46 W m-3 at the HRT of 12 h and 8 h, respectively, showing the adverse effect of increased SDS loading rate on the electrical performance of MFC. This investigation highlighted the importance of HRT in anodic chamber of MFC and offered solution for effective removal of surfactant from wastewater.