Zhiyong Jason Ren

A comprehensive review of microbial electrochemical systems as a platform technology.

Microbial electrochemical systems (MESs) use microorganisms to covert the chemical energy stored in biodegradable materials to direct electric current and chemicals. Compared to traditional treatment-focused, energy-intensive environmental technologies, this emerging technology offers a new and transformative solution for integrated waste treatment and energy and resource recovery, because it offers a flexible platform for both oxidation and reduction reaction oriented processes. All MESs share one common principle in the anode chamber, in which biodegradable substrates, such as waste materials, are oxidized and generate electrical current. In contrast, a great variety of applications have been developed by utilizing this in situ current, such as direct power generation (microbial fuel cells, MFCs), chemical production (microbial electrolysis cells, MECs; microbial electrosynthesis, MES), or water desalination (microbial desalination cells, MDCs). Different from previous reviews that either focus on one function or a specific application aspect, this article provides a comprehensive and quantitative review of all the different functions or system constructions with different acronyms developed so far from the MES platform and summarizes nearly 50 corresponding systems to date. It also provides discussions on the future development of this promising yet early-stage technology.

Practical Energy Harvesting for Microbial Fuel Cells: A Review

The microbial fuel cell (MFC) technology offers sustainable solutions for distributed power systems and energy positive wastewater treatment, but the generation of practically usable power from MFCs remains a major challenge for system scale up and application. Commonly used external resistors will not harvest any usable energy, so energy-harvesting circuits are needed for real world applications. This review summarizes, explains, and discusses the different energy harvesting methods, components, and systems that can extract and condition the MFC energy for direct utilization. This study aims to assist environmental scientists and engineers to gain fundamental understandings of these electronic systems and algorithms, and it also offers research directions and insights on how to overcome the barriers, so the technology can be further advanced and applied in larger scale.

Bioelectrochemical metal recovery from wastewater: a review.

Metal contaminated wastewater posts great health and environmental concerns, but it also provides opportunities for precious metal recovery, which may potentially make treatment processes more cost-effective and sustainable. Conventional metal recovery technologies include physical, chemical and biological methods, but they are generally energy and chemical intensive. The recent development of bioelectrochemical technology provides a new approach for efficient metal recovery, because it offers a flexible platform for both oxidation and reduction reaction oriented processes. While dozens of recent studies demonstrated the feasibility of the bioelectrochemical metal recovery concept, the mechanisms have been different and confusing. This study provides a review that summarizes and discusses the different fundamental mechanisms of metal conversion, with the aim of facilitating the scientific understanding and technology development. While the general approach of bioelectrochemical metal recovery is using metals as the electron acceptor in the cathode chamber and organic waste as the electron donor in the anode chamber, there are so far four mechanisms that have been reported: (1) direct metal recovery using abiotic cathodes; (2) metal recovery using abiotic cathodes supplemented by external power sources; (3) metal conversion using bio-cathodes; and (4) metal conversion using bio-cathodes supplemented by external power sources.

Microbial Metabolism and Community Structure in Response to Bioelectrochemically Enhanced Remediation of Petroleum Hydrocarbon-Contaminated Soil

This study demonstrates that electrodes in a bioelectrochemical system (BES) can potentially serve as a nonexhaustible electron acceptor for in situ bioremediation of hydrocarbon contaminated soil. The deployment of BES not only eliminates aeration or supplement of electron acceptors as in contemporary bioremediation but also significantly shortens the remediation period and produces sustainable electricity. More interestingly, the study reveals that microbial metabolism and community structure distinctively respond to the bioelectrochemically enhanced remediation. Tubular BESs with carbon cloth anode (CCA) or biochar anode (BCA) were inserted into raw water saturated soils containing petroleum hydrocarbons for enhancing in situ remediation. Results show that total petroleum hydrocarbon (TPH) removal rate almost doubled in soils close to the anode (63.5-78.7%) than that in the open circuit positive controls (37.6-43.4%) during a period of 64 days. The maximum current density from the BESs ranged from 73 to 86 mA/m(2). Comprehensive microbial and chemical characterizations and statistical analyses show that the residual TPH has a strongly positive correlation with hydrocarbon-degrading microorganisms (HDM) numbers, dehydrogenase activity, and lipase activity and a negative correlation with soil pH, conductivity, and catalase activity. Distinctive microbial communities were identified at the anode, in soil with electrodes, and soil without electrodes. Uncommon electrochemically active bacteria capable of hydrocarbon degradation such as Comamonas testosteroni, Pseudomonas putida, and Ochrobactrum anthropi were selectively enriched on the anode, while hydrocarbon oxidizing bacteria were dominant in soil samples. Results from genus or phylum level characterizations well agree with the data from cluster analysis. Data from this study suggests that a unique constitution of microbial communities may play a key role in BES enhancement of petroleum hydrocarbons biodegradation in soils.

Bioelectrochemical system platform for sustainable environmental remediation and energy generation.

The increasing awareness of the energy-environment nexus is compelling the development of technologies that reduce environmental impacts during energy production as well as energy consumption during environmental remediation. Countries spend billions in pollution cleanup projects, and new technologies with low energy and chemical consumption are needed for sustainable remediation practice. This perspective review provides a comprehensive summary on the mechanisms of the new bioelectrochemical system (BES) platform technology for efficient and low cost remediation, including petroleum hydrocarbons, chlorinated solvents, perchlorate, azo dyes, and metals, and it also discusses the potential new uses of BES approach for some emerging contaminants remediation, such as CO2 in air and nutrients and micropollutants in water. The unique feature of BES for environmental remediation is the use of electrodes as non-exhaustible electron acceptors, or even donors, for contaminant degradation, which requires minimum energy or chemicals but instead produces sustainable energy for monitoring and other onsite uses. BES provides both oxidation (anode) and reduction (cathode) reactions that integrate microbial-electro-chemical removal mechanisms, so complex contaminants with different characteristics can be removed. We believe the BES platform carries great potential for sustainable remediation and hope this perspective provides background and insights for future research and development.

Biochar as a sustainable electrode material for electricity production in microbial fuel cells

Wood-based biochars were used as microbial fuel cell electrodes to significantly reduce cost and carbon footprint. The biochar was made using forestry residue (BCc) and compressed milling residue (BCp). Side-by-side comparison show the specific area of BCp (469.9m(2)g(-1)) and BCc (428.6cm(2)g(-1)) is lower than granular activated carbon (GAC) (1247.8m(2)g(-1)) but higher than graphite granule (GG) (0.44m(2)g(-1)). Both biochars showed power outputs of 532±18mWm(-2) (BCp) and 457±20mWm(-2) (BCc), comparable with GAC (674±10mWm(-2)) and GG (566±5mWm(-2)). However, lower material expenses made their power output cost 17-35US

Electricity production and microbial biofilm characterization in cellulose-fed microbial fuel cells

W(-1), 90% cheaper than GAC (402US

Microbial electrolysis cells for waste biorefinery: A state of the art review

W(-1)) or GG (392US

Enhanced bioremediation of hydrocarbon-contaminated soil using pilot-scale bioelectrochemical systems

W(-1)). Biochar from waste also reduced the energy and carbon footprint associated with electrode manufacturing and the disposal of which could have additional agronomic benefits.

Microbial community structure accompanied with electricity production in a constructed wetland plant microbial fuel cell

Converting biodegradable materials into electricity, microbial fuel cells (MFCs) present a promising technology for renewable energy production in specific applications. Unlike typical soluble substrates that have been used as electron donors in MFC studies, cellulose is unique because it requires a microbial consortium that can metabolize both an insoluble electron donor (cellulose) and electron acceptor (electrode). In this study, electricity generation and the microbial ecology of cellulose-fed MFCs were analyzed using a defined co-culture of Clostridium cellulolyticum and Geobacter sulfurreducens. Fluorescent in situ hybridization and quantitative PCR showed that when particulate MN301 cellulose was used as sole substrate, most Clostridium cells were found adhered to cellulose particles in suspension, while most Geobacter cells were attached to the electrode. By comparison, both bacteria resided in suspension and biofilm samples when soluble carboxymethyl cellulose was used. This distinct function-related distribution of the bacteria suggests an opportunity to optimize reactor operation by settling cellulose and decanting supernatant to extend cellulose hydrolysis and improve cellulose-electricity conversion.