Search Results (60)

This study introduces an advanced strategy for improving microbial fuel cell (MFC) performance in hexavalent chromium (Cr(VI)) wastewater treatment. A high-performance nano-iron sulfide (nano-FeS) hybridized biocathode was developed by regulating glucose concentration and applying an external voltage. The combination of a glucose concentration of 1000 mg/L and a 0.2 V applied voltage greatly promoted the in situ biosynthesis of nano-FeS, resulting in smaller particle sizes and increased quantities within the biocathode, leading to enhanced electrochemical performance. The MFC with the hybridized biocathode exhibited the highest power density (43.45 ± 1.69 mW/m²) and Cr(VI) removal rate (3.99 ± 0.09 mg/L·h), outperforming the control by 29% and 71%, respectively. The improvements were attributed to the following processes. (1) Nano-FeS provided additional active sites that enhanced electron transfer and electrocatalytic activity, reducing cathode passivation; (2) it protected microorganisms by reducing Cr(VI) toxicity, promoting redox-active substance enrichment and antioxidant enzyme secretion, which maintained microbial activity; (3) the biocathode selectively enriched electroactive and Cr(VI)-reducing bacteria (such as Brucella), fostering a stable and symbiotic microbial community. This study highlights the promising potential of regulating carbon source and external voltage to boost nano-FeS biosynthesis, offering a sustainable and efficient strategy for MFC-based Cr(VI) wastewater treatment with practical implications. Full article

The growing scarcity of freshwater has accelerated the global deployment of desalination technologies, especially reverse osmosis (RO), as an alternative to meet increasing water demands. However, this process generates substantial quantities of brine—a hypersaline waste stream that can severely impact marine ecosystems if improperly managed. This perspective review explores the use of urease-driven Microbially Induced Carbonate Precipitation (MICP) as a biotechnological solution aligned with circular economy principles for the treatment and valorization of RO brines. Through the enzymatic activity of ureolytic microorganisms, MICP promotes the precipitation of calcium carbonate and other mineral phases, enabling the recovery of valuable elements and reducing environmental burdens. Beyond mineral capture, MICP shows promise in the stabilization of toxic metals and potential integration with microbial electrochemical systems for energy applications. This review summarizes current developments, identifies existing challenges, such as microbial performance in saline conditions and reliance on conventional urea sources, and proposes future directions focused on strain optimization, nutrient recycling, and process scalability for sustainable implementation. Full article

Electro-fermentation (EF) is an emerging bioprocess with the ability to regulate the metabolism of electrochemically active microorganisms. In various fermentation processes, electrodes perform either as an electron acceptor or donor, facilitating the formation and movement of electrons and protons. The bioelectric activity created by external electrodes enhances the metabolic reactions, resulting in a higher yield of value-added chemicals. The conventional fermentation process has a number of limitations in terms of usability and economic feasibility, whereas electro-fermentation presents a hybrid technology, minimizing redox instabilities and enhancing the metabolic process in general to achieve increased product production and a higher biomass yield. Electrochemically active microorganisms such as Geobacter and Shewanella species can carry out the exchange of electrons with electrodes directly or indirectly by using electron mediators. Furthermore, the integration of microbial fuel cells (MFCs) with microbial electrolysis cells (MECs) precludes the need for external manipulation of the fermentation system as the required change in electrochemical gradient is provided by the MFC counterpart. The major beneficial aspects of electro-fermentation include its role as a potential tool for enhancing the production of value-added compounds. The mixed-culture system clearly had a favorable impact on the synthesis of butyric acid from rice straw. Furthermore, cathodic electro-fermentation (CEF) exhibited benefits over anaerobic fermentation, influencing NADH/NAD⁺, enabling a higher product titer, and reducing the accumulation of byproducts. Hence, in this review, we emphasize the importance of electro-fermentation over conventional fermentation for biofuel and biochemical production, covering its fundamentals, interactions, types, future challenges, and ability to provide several benefits to boost the fermentation process, such as the process efficiency and product yield, on an industrial scale. Full article

Microbially influenced corrosion (MIC) in anaerobic environments accounts for many severe failures and losses in different industries. Sulfate-reducing bacteria (SRB) represent a typical class of corrosive microorganisms capable of acquiring electrons from steel through extracellular electron transfer processes, thereby inducing severe electrical microbially influenced corrosion (EMIC). Although prior research has underscored the significance of extracellular electron transfer, the contribution of EMIC to the whole MIC has not been comprehensively studied. In this study, Q235 steel coupons were employed in an H-shaped electrochemical cell to conduct electrochemical and coupon immersion experiments, aiming to determine the contribution of EMIC to the overall MIC. The experiments were conducted under two distinct carbon source conditions: 100% carbon source (CS) and 1% CS environments. It was observed that the biotic electrodes exhibited significantly higher cathodic currents, with the most pronounced biological cathodic activity detected in the 100% CS biotic medium. The voltammetric responses of the electrodes before and after changes in the medium confirmed the biocatalytic capability of the attached biofilm in stimulating the cathodic reaction. The proportion of EMIC in MIC was calculated using linear polarization resistance, revealing a trend over time. Additionally, weight loss tests indicated that the contribution of EMIC to the total MIC was approximately 27.69%. Furthermore, the results demonstrated that while the overall corrosion rate was lower in the 1% CS environment, the proportion of EMIC in MIC increased to approximately 37.68%. Full article

A microbial fuel cell (MFC) is a bio-electrochemical system that utilizes electroactive microorganisms to generate electricity. These microorganisms, which convert the energy stored in substrates such as wastewater into electricity, grow on the anode. To ensure biocompatibility, anodes are typically made from carbon-based materials. Therefore, a carbon-based material (by-product of coconut processing) was selected for testing in this study. The anode was prepared by bonding activated coconut carbon with carbon paint on a glass electrode. The aim of this study was to analyze the feasibility of using an electrode prepared in this manner as a surface layer on the anode of an MFC. The performance of an electrode coated only with carbon paint was also evaluated. These two electrodes were compared with a carbon felt electrode, which is commonly used as an anode material in MFCs. In this research, the MFC was fed with a by-product of yeast production, namely a molasses decoction from yeast processing. Measurements were conducted in a standard two-chamber glass MFC with a glass membrane separating the chambers. During the experiment, parameters such as start-up time, cell voltage during MFC start-up, output cell voltage, and power density curves were analyzed. The carbon paint-coated electrode with the activated coconut carbon additive demonstrated operating parameters similar to those of the carbon felt electrode. The results indicate that it is possible to produce electrodes (on a base of by-product of coconut processing) for MFCs using a painting method; however, to achieve a performance comparable to carbon felt, the addition of activated coconut carbon is necessary. This study demonstrates the feasibility of forming a biocompatible layer on various surfaces. Incorporating activated coconut carbon does not complicate the anode fabrication process, as fine ACC grains can be directly applied to the wet carbon paint layer. Additionally, the use of carbon paint as a conductive layer for the active anode in MFCs offers versatility in designing electrodes of various shapes, enabling them to be coated with a suitable active and conductive layer to promote biofilm formation. Moreover, the findings of this study confirm that waste-derived materials can be effectively utilized as electrode components in MFC anodes. The results validate the chosen research approach and emphasize the potential for further investigations in this field, contributing to the development of cost-efficient electrodes derived from by-products for MFC applications. Full article

This study investigates the formation of a protective layer on a 5083 aluminum alloy surface induced by microorganisms from salt marsh. The influence of the initial surface roughness was examined to identify optimal conditions for maximum coverage and thickness of the protective layer. As two opposing effects are suspected, where high surface roughness enhances bacterial adhesion but reduces the resistance to abiotic corrosion, various degrees of roughness were tested. Using electrochemical experiments (OCP measurement, 1/Rp determination, and pitting sensitivity), SEM/TEM observation and EDX characterization, a compromise was found on the initial roughness to obtain a thick protective layer through good bacterial adhesion while minimizing abiotic corrosion. The optimal roughness, achieved through 240-grit grinding, facilitates a uniform distribution of microorganisms and the development of a dense, evenly thick protective layer that significantly enhances the alloy’s resistance to pitting corrosion. The passivity domain doubled when comparing the electrochemical behavior of electrodes immersed in the presence of microbial activity to those immersed without it. Full article

Food safety is a pressing global concern due to the risks posed by contaminants such as pesticide residues, heavy metals, allergens, mycotoxins, and pathogenic microorganisms. While accurate, traditional detection methods like ELISA, HPLC, and mass spectrometry are often time-consuming and resource-intensive, highlighting the need for innovative alternatives. Biosensors based on biological recognition elements such as enzymes, antibodies, and aptamers, offer fast, sensitive, and cost-effective solutions. Using transduction mechanisms like electrochemical, optical, piezoelectric, and thermal systems, biosensors provide versatile tools for detecting contaminants. Advances in DNAzyme- and aptamer-based technologies enable the precise detection of heavy metals, while enzyme- and protein-based biosensors monitor metal-induced changes in biological activity. Innovations like microbial biosensors and DNA-modified electrodes enhance detection accuracy. Biosensors are also highly effective in identifying pesticide residues, allergens, mycotoxins, and pathogens through immunological, enzymatic, and nucleic acid-based techniques. The integration of nanomaterials and bioelectronics has significantly improved the sensitivity and performance of biosensors. By facilitating real-time, on-site monitoring, these devices address the limitations of conventional methods to ensure food quality and regulatory compliance. This review highlights the transformative role of biosensors and how biosensors are improved by emerging technologies in food contamination detection, emphasizing their potential to mitigate public health risks and enhance food safety throughout the supply chain. Full article

Ubiquitous microplastics (MPs) severely affect the efficiency of anaerobic membrane bioreactors (AMBR) for wastewater treatment and energy recovery by inhibiting the metabolic activity of anaerobic microorganisms. The electrochemical system can not only accelerate waste metabolism but also improve microbial resistance by promoting interspecies electron transfer within the system, which has broad application potential in the remediation of MPs wastewater. This paper attempts to evaluate the effect of electrical stimulation on the efficiency of biological wastewater treatment processes containing MPs employing an electrochemical system coupled to an anaerobic membrane bioreactor (ECAMBR). The results showed that although MP exposure inhibited methanogenic performance, electrical stimulation effectively alleviated this inhibitory effect. Further analysis showed that microplastics increased cell damage and affected enzyme activity, but electrical stimulation could affect the stress response of microorganisms, leading to changes in their cell viability and enzyme activities. The 16S-rRNA sequencing indicated that the highest abundance of hydrolytic–acidogenic bacteria Firmicutes and Bacteroidota was found at the phylum level, whereas at the genus level, it was Christensenellaceae_R-7_group, and methanogens were dominated by Methylomonas, Methyloversatilis, and Methylobacter. Functional prediction analysis indicated that carbohydrate metabolism, amino acid metabolism, and energy metabolism were the dominant metabolic pathways and that electrical stimulation could enhance their activities. This study demonstrated the important role of electrochemical stimulation in the remediation of wastewater containing high concentrations of MPs. Full article

A comprehensive investigation into the design and electrochemical optimization of composite electrodes consisting of poly(3,4-ethylenedioxythiophene) (PEDOT)/graphene oxide (GO)/Methanococcus deltae and reduced graphene oxide (rGO)/Methanococcus deltae hybrids, anchored onto stainless-steel (SS) substrates, has been conducted. The GO and rGO materials were synthesized using a modified Hummer method. The resulting SS/PEDOT/GO and SS/PEDOT/rGO composite electrodes were subjected to systematic electrochemical characterization, focusing on the PEDOT p-type and n-type doping/undoping processes within diverse solvent environments (CH₃CN and H₂O) and electrolyte compositions (LiClO₄ and KCl). Raman spectroscopy analysis confirmed the successful integration of graphene derivatives into the electrode structures, while field-emission scanning electron microscopy (FESEM) and atomic force microscopy (AFM) revealed increased surface roughness upon GO and rGO incorporation. This increase in surface roughness is believed to enhance the adhesion of Methanococcus deltae microorganisms and facilitate efficient electron transport. Electrochemical measurements showed that the resulting SS/PEDOT/GO and SS/PEDOT/rGO anodes exhibit remarkable electrocatalytic activity. The SS/PEDOT/GO electrode achieved a maximum power density of 1014.420 mW/cm², while the SS/PEDOT/rGO electrode reached 632.019 mW/cm². Full article

Microbial fuel cells (MFCs) represent a promising technology for sustainable energy generation, which leverages the metabolic activities of microorganisms to convert organic substrates into electrical energy. In oil spill scenarios, hydrocarbonoclastic biofilms naturally form at the water–oil interface, creating a distinct environment for microbial activity. In this work, we engineered a novel MFC that harnesses these biofilms by strategically positioning the positive electrode at this critical junction, integrating the biofilm’s natural properties into the MFC design. These biofilms, composed of specialized hydrocarbon-degrading bacteria, are vital in supporting electron transfer, significantly enhancing the system’s power generation. Next-generation sequencing and scanning electron microscopy were used to characterize the microbial community, revealing a significant enrichment of hydrocarbonoclastic Gammaproteobacteria within the biofilm. Notably, key genera such as Paenalcaligenes, Providencia, and Pseudomonas were identified as dominant members, each contributing to the degradation of complex hydrocarbons and supporting the electrogenic activity of the MFCs. An electrochemical analysis demonstrated that the MFC achieved a stable power output of 51.5 μW under static conditions, with an internal resistance of about 1.05 kΩ. The system showed remarkable long-term stability, which maintained consistent performance over a 5-day testing period, with an average daily energy storage of approximately 216 mJ. Additionally, the MFC effectively recovered after deep discharge cycles, sustaining power output for up to 7.5 h before requiring a recovery period. Overall, the study indicates that MFCs based on hydrocarbonoclastic biofilms provide a dual-functionality system, combining renewable energy generation with environmental remediation, particularly in wastewater treatment. Despite lower power output compared to other hydrocarbon-degrading MFCs, the results highlight the potential of this technology for autonomous sensor networks and other low-power applications, which required sustainable energy sources. Moreover, the hydrocarbonoclastic biofilm-based MFC presented here offer significant potential as a biosensor for real-time monitoring of hydrocarbons and other contaminants in water. The biofilm’s electrogenic properties enable the detection of organic compound degradation, positioning this system as ideal for environmental biosensing applications. Full article

Microbial electrochemical cells (MxCs) offer a sustainable approach for wastewater treatment and energy recovery by harnessing the electroactive properties of microorganisms. This study explores the enrichment of Geobacter species on anode biofilms in single-(S-MxCs) and double-chambered (D-MxCs) MxCs, using domestic wastewater without an external anode potential. Stable current densities were achieved within 10 days for S-MxCs (9.52 ± 0.8 A/m²) and 14 days for D-MxCs (4.28 ± 0.9 A/m²), with S-MxCs showing a superior electrochemical performance. Hydrogen production rates were higher in D-MxCs (14.93 ± 0.66 mmol H₂/L/day) compared to S-MxCs (9.46 ± 0.8 mmol H₂/L/day), with cumulative production rates of 12.9 ± 1.3 mmol H₂/g COD and 6.48 ± 1.4 mmol H₂/g COD, respectively. Cyclic voltammetry confirmed enhanced bioelectrocatalytic activity in S-MxCs, while SEM imaging showed denser biofilms on S-MxC anodes. The novelty of this study lies in its demonstration of efficient biofilm development and microbial community resilience under non-potentialized conditions, providing insights that advance the practical application of MxCs in environmental biotechnology. Full article

Microbial fuel cells (MFCs) can realize the conversion of chemical energy to electrical energy in high-salt wastewater, but the easily deactivated cathode seriously affects the performance of MFCs. To enhance the stability and sustainability of MFC in such circumstances, a bimetallic organic framework ZIF-8/ZIF-67 was utilized for the synthesis of a carbon cage-encapsulated metal catalysts in this study. Catalysts with different Co and Ce ratio (Co@C (without the Ce element), CoCe_0.25@C, CoCe_0.5@C, and CoCe₁@C) were employed to modify the activated carbon cathodes of MFCs. The tests demonstrated that the MFCs with the CoCe_0.5@C cathode catalyst obtained the highest maximum power density (188.93 mW/m²) and the smaller polarization curve slope, which boosted the electrochemical activity of microorganisms attached to the anode. The appropriate addition of the Ce element was conductive to the stability of the catalyst’s active center, which is beneficial for the stability of catalytic performance. Under the function of the CoCe_0.5@C catalyst, the MFCs exhibited superior and stable norfloxacin (NOR) degradation efficiency. Even after three cycles, the NOR degradation rate remained at 68%, a negligible 5.6% lower than the initial stage. Furthermore, based on the analysis of microbial diversity, the abundance of electrogenic microorganisms on a bioanode is relatively high with CoCe_0.5@C as the cathode catalyst. This may be because the better cathode oxygen reduction reaction (ORR) performance can strengthen the metabolic activity of anode microorganisms. The electrochemical performance and NOR degradation ability of MFC were enhanced in a high-salt environment. This paper provides an approach to address the challenge of the poor salt tolerance of cathode catalysts in MFC treatment, and presents a new perspective on resource utilization, low carbon emissions, and the sustainable treatment of high-salt wastewater. Full article

Microbial electrochemical systems that integrate the advantages of inorganic electrocatalysis and microbial catalysis are expected to provide sustainable solutions to the increasing energy shortages, resource depletion, and climate degradation. However, sluggish extracellular electron transfer (EET) at the interface between electroactive microorganisms and inorganic electrode materials is a critical bottleneck that limits the performance of systems. Electrocatalytic nanomaterials are highly competitive in overcoming this obstacle due to their effective association with microbial catalysis. Therefore, this review focuses on the cutting-edge applications and enhancement mechanisms of nanomaterials with electrocatalytic activity in promoting microbial EET. First, the EET mechanism of microbial electrocatalysis in both microbial anodes and cathodes is briefly introduced, and then recent applications of various electrocatalytic nanomaterials in diverse microbial electrochemical systems are summarized, including heteroatom-doped carbons and precious metal, as well as transition metal oxides, sulfides, carbides, and nitrides. The synergistic effects of nanomaterial electrocatalysis and microbial catalysis on enhancing interfacial EET are analyzed. Finally, the challenges and perspectives of realizing high-performance microbial electrochemical systems are also discussed in order to offer some reference for further research. Full article

The wastewater produced by the pharmaceutical industry is highly organic and toxic. Dual-chambered microbial fuel cells (DMFCs) may represent a sustainable solution to process wastewater while simultaneously recovering its energy content. DMFCs are bio-electrochemical devices that employ microorganisms to transform the chemical energy of organic compounds into electrical energy. This study aims to demonstrate the feasibility of a DMFC with a manganese cobalt oxide-coated activated carbon fiber felt (MnCo₂O₄-ACFF) electrode to treat pharmaceutical industry wastewater (PW) and exploit its energy content. The proposed technology is experimentally investigated considering the effect of the organic load (OL) on the system performance in terms of organic content removal and electricity production. As per the experimental campaign results, the optimum OL for achieving maximum removal efficiencies for total chemical oxygen demand, soluble oxygen demand, and total suspended solids was found to be 2 g COD/L. At this value of OL, the highest current and power densities of 420 mA/m² and 348 mW/m² were obtained. Therefore, based on the outcomes of the experimental campaign, the (MnCo₂O₄-ACFF) electrode DMFC technique was found to be a sustainable and effective process for the treatment and energy recovery from PW. Full article

Advanced Oxidation Processes (AOPs) offer promising methods for disinfection by generating radical species like hydroxyl radicals, superoxide anion radicals, and hydroxy peroxyl, which can induce oxidative stress and deactivate bacterial cells. Photocatalysis, a subset of AOPs, activates a semiconductor using specific electromagnetic wavelengths. A novel material, Cu/Cu₂O/CuO nanoparticles (NPs), was synthesized via a laser ablation protocol (using a 1064 nm wavelength laser with water as a solvent, with energy ranges of 25, 50, and 80 mJ for 10 min). The target was sintered from 100 °C to 800 °C at rates of 1.6, 1.1, and 1 °C/min. The composite phases of Cu, CuO, and Cu₂O showed enhanced photocatalytic activity under visible-light excitation at 368 nm. The size of Cu/Cu₂O/CuO NPs facilitates penetration into microorganisms, thereby improving the disinfection effect. This study contributes to synthesizing mixed copper oxides and exploring their activation as photocatalysts for cleaner surfaces. The electronic and electrochemical properties have potential applications in other fields, such as capacitor materials. The laser ablation method allowed for modification of the band gap absorption and enhancement of the catalytic properties in Cu/Cu₂O/CuO NPs compared to precursors. The disinfection of E. coli with Cu/Cu₂O/CuO systems serves as a case study demonstrating the methodology’s versatility for various applications, including disinfection against different microorganisms, both Gram-positive and Gram-negative. Full article