Search Results (56)

This study explores the feasibility of producing biohydrogen from winery wastewater using a dual-chamber microbial electrolysis cell (MEC). A mixed microbial consortium pre-adapted to heavy-metal environments and enriched with Geobacter sulfurreducens was anaerobically cultivated from diverse waste streams. Over 5000 h of development, the MEC system was progressively adapted to winery wastewater, enabling long-term electrochemical stability and high organic matter degradation. Upon winery wastewater addition (5% v/v), the system achieved a sustained hydrogen production rate of (0.7 ± 0.3) L H₂ L⁻¹ d⁻¹, with an average current density of (60 ± 4) A m⁻³, and COD removal efficiency exceeding 55%, highlighting the system’s resilience despite the presence of inhibitory compounds. Coulombic efficiency and cathodic hydrogen recovery reached (75 ± 4)% and (87 ± 5)%, respectively. Electrochemical impedance spectroscopy provided mechanistic insight into charge transfer and biofilm development, correlating resistive parameters with biological adaptation. These findings demonstrate the potential of MECs to simultaneously treat agro-industrial wastewaters and recover energy in the form of hydrogen, supporting circular resource management strategies. 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

Microbiologically influenced corrosion (MIC) is one of the key causes of material failure in marine engineering, and sulfate-reducing bacteria (SRB) and iron-oxidizing bacteria (IOB) are typical representatives of anaerobic and aerobic microorganisms, respectively. These microorganisms are widely present in marine environments and can form synergistic communities on the surface of metal materials, posing a corrosion threat to them. At the same time, the presence of mixed bacteria may have an effect on cathodic protection, so this study investigates the growth metabolism of mixed SRB and IOB under different cathodic protection potentials in an impressed current cathodic protection (ICCP) system in a marine environment containing SRB and IOB. It also examines the attachment of these microorganisms to the anode and cathode, and the impact on cathodic protection efficiency. The results indicate that in a marine environment containing IOB and SRB, the cathodic protection efficiency of the ICCP system increases with the negative shift of the protection potential. A more positive cathodic protection potential promotes the adhesion of mixed bacteria on the electrode surface and the formation of a biofilm, which reduces cathodic protection efficiency. In contrast, at a cathodic protection potential of −1.05 V (SCE), bacterial growth is inhibited, and a dense crystalline corrosion film primarily composed of Fe₂O₃ and Fe(OH)₃ forms on the cathode surface. This film effectively protects the cathodic metal, significantly mitigating MIC. Full article

Traditional anaerobic digestion (AD) technology continues to have severe limitations in terms of complicated substrate degradation efficiency and methane production. This study optimizes the AD system using corn straw and cattle manure as substrates by introducing an exogenous N-Hexanoyl-L-Homoserine lactone (C6-HSL) signaling molecule in concert with an applied external voltage of 0.8 V, systematically investigating its impact on methanogenic performance and microbial community dynamics. The results show that the combined regulation significantly increased methane production (by 29.74%) and substrate utilization rate (by 74.73%) while preventing acid inhibition and ammonia nitrogen inhibition. Mechanistic analysis revealed that the external voltage enhanced the system’s electrocatalytic activity, while the C6-HSL signaling molecule further facilitated the electron transfer efficiency of the biofilm on the electrode. The combined regulation notably enriched hydrogenotrophic methanogens (with Methanobacterium predominating on the cathode and Methanobrevibacter in the digestate), establishing a stable metabolic cooperative network on both the electrode and in the digestate, optimizing the hydrogenotrophic methanogenesis pathway, and enhancing the synergistic effects among microbial communities and system robustness. This study uncovers the synergistic enhancement mechanism of C6-HSL and external voltage, providing new technological pathways and theoretical support for the efficient conversion of low-quality biomass resources and the production of clean energy. Full article

Microalgae microbial fuel cells (pMFCs) are distinguished by their ability to combine waste utilization with the simultaneous recovery of energy and valuable materials. The generation of high current density is linked to the efficient electron transfer to the anode via the anodic biofilm and the high photosynthetic activity of the microalgae cultivated in the cathode chamber. This review explores the impact of wastewater type on energy production and wastewater treatment. Additionally, it discusses the challenges related to microalgae growth in the cathode chamber, the necessity of aeration, and the sequestration of carbon dioxide from the anode chamber. The efficiency of microalgae in utilizing nutrients from various types of wastewater is also presented. In conclusion, the comparison between wastewater treatment and energy balance in pMFCs and conventional wastewater treatment plants is provided. On average, MFCs consume only 0.024 kW or 0.076 kWh/kg COD, which is approximately ten times less than the energy used by activated sludge bioprocesses. This demonstrates that MFCs offer highly efficient energy consumption compared to traditional wastewater treatment systems while simultaneously recovering energy through exoelectrogenic, bioelectrochemical processes. Full article

Optimal product synthesis in bioelectrochemical systems (BESs) requires a comprehensive understanding of the relationship between external voltage and microbial yield. While most studies assume constant growth yields or rely on empirical estimates, this study presents a novel thermodynamic model, linking anodic oxidation and cathodic carbon dioxide (${CO}_2$) reduction to methane (${CH}_4$) by growing microbial biofilm. Through integrating theoretical Gibbs free energy calculations, the model predicts electron and proton transfers for autotrophic methanogen and anode-respiring bacteria (ARB) growth, accounting for varying applied voltages and substrate concentrations. The findings identify an optimal applied cathodic potential of −0.3 V vs. the standard hydrogen electrode (SHE) for maximizing ${CH}_4$ production under standard conditions (pH 7, 25 °C, 1 atm) regardless of ohmic losses. The model bridges the stoichiometry of anodic and cathodic biofilms, addressing research gaps in simulating anodic and cathodic biofilm growth simultaneously. Additionally, sensitivity analyses reveal that lower substrate concentrations require more negative voltages than standard condition to stimulate microbial growth. The model was validated using experimental data, demonstrating reasonable predictions of biomass growth and ${CH}_4$ yield under different operating voltages in a multi substrate system. The results show that higher voltage inputs increase biomass yield while reducing ${CH}_4$ output due to non-optimal voltage. This validated model provides a tool for optimizing BES performance to enhance ${CH}_4$ recovery and biofilm stability. These insights contribute to finding optimum voltage for the highest ${CH}_4$ production for energy efficient ${CO}_2$ reduction for scaling up BES technology. Full article

This study explores the efficient decolorization and complete mineralization of the diazo dye Evans blue, using an integrated aerobic bioreactor system coupled with a double-chamber microbial fuel cell (DCMFC) including a bio-cathode and acetate as a cosubstrate. The research addresses the environmental challenges posed by dye-laden industrial effluents, focusing on achieving high decolorization efficiency and understanding the microbial communities involved. The study utilized mixed strains of actinomycetes, isolated from garden compost, to treat initial dye concentrations of 100 mg/L and 200 mg/L. Decolorization efficiency and microbial community composition were evaluated using 16S rRNA sequencing, and electrochemical impedance spectroscopy (EIS) was used to assess anode and DCMFC resistance. The results demonstrated decolorization efficiencies ranging from 90 ± 2% to 98 ± 1.9% for 100 mg/L and from 79 ± 2% to 87% ± 1% for 200 mg/L. An anode resistance of 12.48 Ω indicated a well-developed biofilm and enhanced electron transfer. The microbial community analysis revealed a significant presence of Pseudomonadota (45.5% in dye-acclimated cultures and 32% in inoculum cultures), with key genera including Actinomarinicola (13.75%), Thermochromatium (4.82%), and Geobacter (4.52%). This study highlights the potential of the integrated DCMFC–aerobic system, utilizing mixed actinomycetes strains, for the effective treatment of industrial dye effluents, offering both environmental and bioenergy benefits. Full article

Microbial metal corrosion has become an important topic in metal research, which is one of the main causes of equipment damage, energy loss, and economic loss. At present, the research on microbial metal corrosion focuses on the characteristics of corrosion products, the environmental conditions affecting corrosion, and the measures and means of corrosion prevention, etc. In contrast, the main microbial taxa involved in metal corrosion, their specific role in the corrosion process, and the electron transfer pathway research are relatively small. This paper summarizes the mechanism of microbial carbon steel corrosion caused by SRB, including the cathodic depolarization theory, acid metabolite corrosion theory, and the biocatalytic cathodic sulfate reduction mechanism. Based on the reversible nature of electron transfer in biofilms and the fact that electrons must pass through the extracellular polymers layer between the solid electrode and the cell, this paper focuses on three types of electrochemical mechanisms and electron transfer modes of extracellular electron transfer occurring in microbial fuel cells, including direct-contact electron transfer, electron transfer by conductive bacterial hair proteins or nanowires, and electron shuttling mediated by the use of soluble electron mediators. Finally, a more complete pathway of electron transfer in microbial carbon steel corrosion due to SRB is presented: an electron goes from the metal anode, through the extracellular polymer layer, the extracellular membrane, the periplasm, and the intracellular membrane, to reach the cytoplasm for sulfate allosteric reduction. This article also focuses on a variety of complex components in the extracellular polymer layer, such as extracellular DNA, quinoline humic acid, iron sulfide (FeS_X), Fe³⁺, etc., which may act as an extracellular electron donor to provide electrons for the SRB intracellular electron transfer chain; the bioinduced mineralization that occurs in the SRB biofilm can inhibit metal corrosion, and it can be used for the development of green corrosion inhibitors. This provides theoretical guidance for the diagnosis, prediction, and prevention of microbial metal corrosion. Full article

The use of gas diffusion electrodes (GDEs) in microbial fuel cells (MFCs) can improve their cell performance, but tends to cause fouling. In order to allow long-term stable operation, the search for antifouling methods is necessary. Therefore, an antibacterial coating with ammonium compounds is investigated. Within the first 30 days of operation, the maximum measured power density of a GDE with antibacterial ionomer was 606 mW m⁻². The GDE without an antifouling treatment could only reach a maximum of 284 mW m⁻². Furthermore, there was an optimum in the loading amount with ionomer below 2.6 mg cm⁻². Further investigations showed that additional aeration of the GDEs by a fan had a negative effect on their performance. Despite the higher performance, the antibacterial coating could not prevent biofilm growth at the surface of the GDE. The thickness of the biofilm was only reduced by 14–16%. However, the weight of the biofilm on the treated GDEs was 62–80% less than on a GDE without an antifouling treatment. Consequently, the coating cannot completely prevent fouling, but possibly leads to a lower density of the biofilm or prevents clogging of the pores inside the electrodes and improves their long-term stability. Full article

The increasing global water pollution leads to the need for urgent development of rapid and accurate water quality monitoring methods. Microbial fuel cells (MFCs) have emerged as real-time biosensors for biochemical oxygen demand (BOD), but they grapple with several challenges, including issues related to reproducibility, operational stability, and cost-effectiveness. These challenges are substantially shaped by the selection of an appropriate air-breathing cathode. Previous studies indicated a critical influence of the cathode on both the enduring electrochemical performance of MFCs and the taxonomic diversity at the electroactive anode. However, the effect of different gas diffusion electrodes (GDE) on 3D-printed single-chamber MFCs for BOD biosensing application and its effect on the bioelectroactive anode was not investigated before. Our study focuses on comparing GDE cathode materials to enhance MFC performance for precise and rapid BOD analysis in wastewater. We examined for over 120 days two Pt-coated air-breathing cathodes with distinct carbonaceous gas diffusion layers (GDLs) and catalyst layers (CLs): cost-effective carbon paper (CP) with hand-coated CL and more expensive woven carbon cloth (CC) with CL pre-applied by the supplier. The results show significant differences in electrochemical characteristics and anodic biofilm composition between MFCs with CP and CC GDE cathodes. CP-MFCs exhibited lower sensitivity (16.6 C L mg⁻¹ m⁻²) and a narrower dynamic range (25 to 600 mg L⁻¹), attributed to biofouling-related degradation of the GDE. In contrast, CC-MFCs demonstrated superior performance with higher sensitivity (37.6 C L mg⁻¹ m⁻²) and a broader dynamic range (25 to 800 mg L⁻¹). In conclusion, our study underscores the pivotal role of cathode selection in 3D-printed MFC biosensors, influencing anodic biofilm enrichment time and overall BOD assessment performance. We recommend the use of cost-effective CP GDL with hand-coated CL for short-term MFC biosensor applications, while advocating for CC GDL supplied with CL as the preferred choice for long-term sensing implementations with enduring reliability. Full article

Tetrahedral amorphous carbon (taC) is a hydrogen-free carbon with extensive properties such as hardness, optical transparency, and chemical inertness. taC coatings have attracted much attention in recent times, as have coatings doped with a noble metal. A known antimicrobial metal agent, silver (Ag), has been used as a dopant in taC, with different Ag concentrations on the Ti64 coupons using a hybrid filtered cathodic vacuum arc (FCVA) and magnetron sputtering system. The physiochemical properties of the coated surface were investigated using spectroscopic and electron microscopy techniques. A doping effect of Ag-taC on biofilm formation was investigated and found to have a significant effect on the bacterial-biofilm-forming bacteria Staphylococcus aureus and Pseudomonas aeruginosa depending on the concentration of Ag. Further, the effect of coated and uncoated Ag-taC films on a pathogenic bacterium was examined using SEM. The result revealed that the Ag-taC coatings inhibited the biofilm formation of S. aureus. Therefore, this study demonstrated the possible use of Ag-taC coatings against biofilm-related complications on medical devices and infections from pathogenic bacteria. Full article

Regenerated water serves as a supplementary source for circulating cooling water systems, but it often fosters microbial growth within pipelines. Given its widespread use as a corrosion inhibitor, understanding HEDP’s efficacy in microbial environments and its impact on microorganisms is imperative. This study established an iron bacterial system by isolating and enriching iron bacteria. Through a comprehensive approach incorporating corrosion weight loss analysis, XPS analysis, SEM electron microscopy, as well as microbial and electrochemical testing, the corrosion inhibition behavior and mechanism of HEDP within the iron bacterial system were investigated. The findings reveal that within the iron bacterial system, HEDP achieves a corrosion inhibition rate of 76% following four distinct stages—weakening, strengthening, stabilizing, and further strengthening—underscoring its robust corrosion inhibition capability. Moreover, HEDP enhances the density of biofilms and elevates the activation energy of carbon steel interfaces. It alternates with oxygen to continuously suppress the activity of IRB while gradually inhibiting the activity of IOB. This process culminates in a corrosion inhibition mechanism where cathodic inhibition predominates, supported by anodic inhibition as a complementary mechanism. Full article

Agroindustry waste has exponentially increased in recent years, generating economic losses and environmental problems. In addition, new ways to generate sustainable alternative electrical energy are currently being sought to satisfy energy demand. This investigation proposes using avocado waste as fuel for electricity generation in single-chamber MFCs. The avocado waste initially operated with an ambient temperature (22.4 ± 0.01 °C), DO of 2.54 ± 0.01 mg/L, TDS of 1358 ± 1 mg/L and COD of 1487.25 ± 0.01 mg/L. This research managed to generate its maximum voltage (0.861 ± 0.241 V) and current (3.781 ± 0.667 mA) on the fourteenth day, operating at an optimal pH of 7.386 ± 0.147, all with 126.032 ± 8.888 mS/cm of electrical conductivity in the substrate. An internal resistance of 67.683 ± 2.456 Ω was found on day 14 with a PD of 365.16 ± 9.88 mW/cm² for a CD of 5.744 A/cm². Micrographs show the formation of porous biofilms on both the anodic and cathodic electrodes. This study gives preliminary results of using avocado waste as fuel, which can provide outstanding solutions to agro-industrial companies dedicated to selling this fruit. Full article

The management of drainage water (DW), which is produced during the soilless cultivation of plants, requires a high energy input. At the same time, DW is characterized by a high electrolytic conductivity, a high redox potential, and is also stable and putrefaction-free. In the present study, the natural properties of drainage water and a biotreatment method employing an external organic substrate in the form of citric acid (C/N 1.0, 1.5, 2.0) were utilized for energy recovery by a microbial fuel cell (MFC). The cathode chamber served as a retention tank for DW with a carbon felt electrode fixed inside. In turn, a biological reactor with biomass attached to the filling in the form of carbon felt served as the anode chamber. The filling also played the role of an electrode. The chambers were combined by an ion exchange membrane, forming an H letter-shaped system. They were then connected in an external electrical circuit with a resistance of 1k Ω. The use of a flow-through system eliminated steps involving aeration and mixing of the chambers’ contents. Citric acid was found to be an efficient organic substrate. The voltage of the electric current increased from 44.34 ± 60.92 mV to 566.06 ± 2.47 mV for the organic substrate dose expressed by the C/N ratio ranging from 1.0 to 2.0. At the same time, the denitrification efficiency ranged from 51.47 ± 9.84 to 95.60 ± 1.99% and that of dephosphatation from 88.97 ± 2.41 to 90.48 ± 1.99% at C/N from 1.0 to 2.0. The conducted studies confirmed the possibility of recovering energy during the biological purification of drainage water in a biofilm reactor. The adopted solution only required the connection of electrodes and tanks with an ion-selective membrane. Further research should aim to biologically treat DW followed by identification of the feasibility of energy recovery by means of MFC. Full article

Acetate can be produced from carbon dioxide (CO₂) and electricity using bacteria at the cathode of microbial electrosynthesis (MES). This process relies on electrolytically-produced hydrogen (H₂). However, the low solubility of H₂ can limit the process. Using metal cathodes to generate H₂ at a high rate can improve MES. Immobilizing bacteria on the metal cathode can further proliferate the H₂ availability to the bacteria. In this study, we investigated the performances of 3D bioprinting of Sporomusa ovata on three metal meshes—copper (Cu), stainless steel (SS), and titanium (Ti), when used individually as a cathode in MES. Bacterial cells were immobilized on the metal using a 3D bioprinter with alginate hydrogel ink. The bioprinted Ti mesh exhibited higher acetate production (53 ± 19 g/m²/d) at −0.8 V vs. Ag/AgCl as compared to other metal cathodes. More than 9 g/L of acetate was achieved with bioprinted Ti, and the least amount was obtained with bioprinted Cu. Although all three metals are known for catalyzing H₂ evolution, the lower biocompatibility and chemical stability of Cu hampered its performance. Stable and biocompatible Ti supported the bioprinted S. ovata effectively. Bioprinting of synthetic biofilm on H₂-evolving metal cathodes can provide high-performing and robust biocathodes for further application of MES. Full article