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Dive into the research topics where Bruce E. Logan is active.

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Featured researches published by Bruce E. Logan.


Nature Reviews Microbiology | 2009

Exoelectrogenic bacteria that power microbial fuel cells

Bruce E. Logan

There has been an increase in recent years in the number of reports of microorganisms that can generate electrical current in microbial fuel cells. Although many new strains have been identified, few strains individually produce power densities as high as strains from mixed communities. Enriched anodic biofilms have generated power densities as high as 6.9 W per m2 (projected anode area), and therefore are approaching theoretical limits. To understand bacterial versatility in mechanisms used for current generation, this Progress article explores the underlying reasons for exocellular electron transfer, including cellular respiration and possible cell–cell communication.


Science | 2012

Conversion of Wastes into Bioelectricity and Chemicals by Using Microbial Electrochemical Technologies

Bruce E. Logan; Korneel Rabaey

Waste biomass is a cheap and relatively abundant source of electrons for microbes capable of producing electrical current outside the cell. Rapidly developing microbial electrochemical technologies, such as microbial fuel cells, are part of a diverse platform of future sustainable energy and chemical production technologies. We review the key advances that will enable the use of exoelectrogenic microorganisms to generate biofuels, hydrogen gas, methane, and other valuable inorganic and organic chemicals. Moreover, we examine the key challenges for implementing these systems and compare them to similar renewable energy technologies. Although commercial development is already underway in several different applications, ranging from wastewater treatment to industrial chemical production, further research is needed regarding efficiency, scalability, system lifetimes, and reliability.


Deep-sea Research Part I-oceanographic Research Papers | 1993

The abundance and significance of a class of large, transparent organic particles in the ocean

Alice L. Alldredge; Uta Passow; Bruce E. Logan

Polysaccharide-specific staining techniques reveal the existence and high abundance of a class of large, discrete, transparent particles in seawater and diatom cultures formed from dissolved exopolymers exuded by phytoplankton and bacteria. Transparent exopolymer particles (TEP), ranged from 28 to 5000 particles ml−1 and 3 to 100s μm in longest dimension at five coastal stations off California. A high percentage of seemingly free-living bacteria (28–68%) were attached to these transparent sheets and films, suggesting that they may alter the distributions and microenvironments of marine microbes in nature. Preliminary coagulation experiments demonstrated that TEP are major agents in the aggregation of diatoms and in the formation of marine snow. The existence of microbial exudates acting as large, discrete particles, rather than as dissolved molecules or as coating on other particles, suggests that the transformation of dissolved organic matter into particulate form in the sea can occur via a rapid abiotic pathway as well as through conventional microbial uptake. The existence of these particles has far reaching implications for food web structure, microbial processes, carbon cycling and particulate flux in the ocean.


Nature | 2012

Membrane-based processes for sustainable power generation using water

Bruce E. Logan; Menachem Elimelech

Water has always been crucial to combustion and hydroelectric processes, but it could become the source of power in membrane-based systems that capture energy from natural and waste waters. Two processes are emerging as sustainable methods for capturing energy from sea water: pressure-retarded osmosis and reverse electrodialysis. These processes can also capture energy from waste heat by generating artificial salinity gradients using synthetic solutions, such as thermolytic salts. A further source of energy comes from organic matter in waste waters, which can be harnessed using microbial fuel-cell technology, allowing both wastewater treatment and power production.


Proceedings of the National Academy of Sciences of the United States of America | 2007

Sustainable and efficient biohydrogen production via electrohydrogenesis

Shaoan Cheng; Bruce E. Logan

Hydrogen gas has tremendous potential as an environmentally acceptable energy carrier for vehicles, but most hydrogen is generated from nonrenewable fossil fuels such as natural gas. Here, we show that efficient and sustainable hydrogen production is possible from any type of biodegradable organic matter by electrohydrogenesis. In this process, protons and electrons released by exoelectrogenic bacteria in specially designed reactors (based on modifying microbial fuel cells) are catalyzed to form hydrogen gas through the addition of a small voltage to the circuit. By improving the materials and reactor architecture, hydrogen gas was produced at yields of 2.01–3.95 mol/mol (50–99% of the theoretical maximum) at applied voltages of 0.2 to 0.8 V using acetic acid, a typical dead-end product of glucose or cellulose fermentation. At an applied voltage of 0.6 V, the overall energy efficiency of the process was 288% based solely on electricity applied, and 82% when the heat of combustion of acetic acid was included in the energy balance, at a gas production rate of 1.1 m3 of H2 per cubic meter of reactor per day. Direct high-yield hydrogen gas production was further demonstrated by using glucose, several volatile acids (acetic, butyric, lactic, propionic, and valeric), and cellulose at maximum stoichiometric yields of 54–91% and overall energy efficiencies of 64–82%. This electrohydrogenic process thus provides a highly efficient route for producing hydrogen gas from renewable and carbon-neutral biomass resources.


Deep-sea Research Part I-oceanographic Research Papers | 1994

The role of particulate carbohydrate exudates in the flocculation of diatom blooms

Uta Passow; Alice L. Alldredge; Bruce E. Logan

Diatom blooms are frequently terminated by mass aggregation of cells into large, rapidly sinking aggregates. It has been hypothesized that transparent exopolymer particles (TEP), abundant particles formed from the polysaccharides exuded by living cells, may be essential for this mass flocculation processes. We investigated the abundance of TEP and their role in the aggregation of diatoms in laboratory cultures and during a natural diatom bloom off California. TEP and dissolved carbohydrates accumulated appreciably over the growth cycle of Chaetoceros gracilis in the laboratory. The flocculation of C. gracilis in a laboratory flocculator was dominated by TEP, not cells, and large flocs, consisting predominantly of particulate polysaccharides, formed at a rate more than an order of magnitude higher than predicted by coagulation theory for cells alone. The frequency of interparticle attachment was three orders of magnitude higher for TEP than for cells. The pattern of flocculation of a natural diatom bloom was similar to that of laboratory cultures. Prior to bloom flocculation the abundance and total quantity of TEP and the concentration of particulate carbohydrates increased, while dissolved carbohydrate concentrations decreased. During the flocculation stage TEP aggregated into fewer, but much larger particles and concentrations of dissolved carbohydrates decreased further. The percentage of diatom cells which were attached to TEP increased during the flocculation period from 3 to 90% and TEP formed the matrix of all the natural diatom aggregates observed. During the late flocculation stage the quantity of TEP and TEP aggregates did not increase further and concentrations of diatoms decreased, presumably because large flocs sank out. Our findings indicate that TEP should be included in models of particle aggregation in the ocean. The abundance, large size and high sticking coefficient of TEP make them essential to the aggregation of diatom blooms. The extracellular release of polysaccharides by growing cells may be an adaptation for aggregation. The abiotic formation of particulate organic matter (TEP) from dissolved organic matter (DOC) may help to explain the extremely high turnover rates of DOC observed during blooms.


Bioresource Technology | 2010

Effectiveness of domestic wastewater treatment using microbial fuel cells at ambient and mesophilic temperatures.

Young-Ho Ahn; Bruce E. Logan

Domestic wastewater treatment was examined under two different temperature (23+/-3 degrees C and 30+/-1 degrees C) and flow modes (fed-batch and continuous) using single-chamber air-cathode microbial fuel cells (MFCs). Temperature was an important parameter for treatment efficiency and power generation. The highest power density of 422 mW/m(2) (12.8 W/m(3)) was achieved under continuous flow and mesophilic conditions, at an organic loading rate of 54 g COD/L-d, achieving 25.8% COD removal. Energy recovery was found to depend significantly on the operational conditions (flow mode, temperature, organic loading rate, and HRT) as well as the reactor architecture. The results demonstrate that the main advantages of using temperature-phased, in-series MFC configurations for domestic wastewater treatment are power savings, low solids production, and higher treatment efficiency.


Environmental Science & Technology | 2009

Separator characteristics for increasing performance of microbial fuel cells.

Xiaoyuan Zhang; Shaoan Cheng; Xin Wang; Xia Huang; Bruce E. Logan

Two challenges for improving the performance of air cathode, single-chamber microbial fuel cells (MFCs) include increasing Coulombic efficiency (CE) and decreasing internal resistance. Nonbiodegradable glass fiber separators between the two electrodes were shown to increase power and CE, compared to cloth separators (J-cloth) that were degraded over time. MFC tests were conducted using glass fiber mats with thicknesses of 1.0 mm (GF1) or 0.4 mm (GF0.4), a cation exchange membrane (CEM), and a J-cloth (JC), using reactors with different configurations. Higher power densities were obtained with either GF1 (46 +/- 4 W/m(3)) or JC (46 +/- 1 W/m(3)) in MFCs with a 2 cm electrode spacing, when the separator was placed against the cathode (S-configuration), rather than MFCs with GF0.4 (36 +/- 1 W/m(3)) or CEM (14 +/- 1 W/m(3)). Power was increased to 70 +/- 2 W/m(3) by placing the electrodes on either side of the GF1 separator (single separator electrode assembly, SSEA) and further to 150 +/- 6 W/m(3) using two sets of electrodes spaced 2 cm apart (double separator electrode assembly, DSEA). Reducing the DSEA electrode spacing to 0.3 cm increased power to 696 +/- 26 W/m(3) as a result of a decrease in the ohmic resistance from 5.9 to 2.2 Omega. The main advantages of a GF1 separator compared to JC were an improvement in the CE from 40% to 81% (S-configuration), compared to only 20-40% for JC under similar conditions, and the fact that GF1 was not biodegradable. The high CE for the GF1 separator was attributed to a low oxygen mass transfer coefficient (k(O) = 5.0 x 10(-5) cm/s). The GF1 and JC materials differed in the amount of biomass that accumulated on the separator and its biodegradability, which affected long-term power production and oxygen transport. These results show that materials and mass transfer properties of separators are important factors for improving power densities, CE, and long-term performance of MFCs.


Bioremediation Journal | 1998

A Review of Chlorate- and Perchlorate-Respiring Microorganisms

Bruce E. Logan

Chlorate (CIO3 −) and perchlorate (CIO4 −) have been manufactured in large quantities, and therefore it is not surprising that they have been found at high concentrations (>50 mg/L and >1000 mg/L, respectively) in surface waters and groundwaters around the world. These compounds are chemically stable in water, and they are difficult to remove using typical physical-chemical water treatment technologies. Fortunately, chlorate and perchlorate can be removed by biodegradation to low levels in water. Both compounds are highly oxidized and can serve as electron acceptors for several strains of microorganisms under anoxic conditions. Although it has been known for more than 40 years that chlorate can be reduced by mixed cultures, several bacteria have been isolated recently that are able to respire using either chlorate or perchlorate. The purpose of this paper is to review the characteristics of these mixed cultures and isolates in order to assess their future potential for biological water and wastewater trea...


Biotechnology and Bioengineering | 2009

Energy from algae using microbial fuel cells

Sharon B. Velasquez-Orta; Thomas P. Curtis; Bruce E. Logan

Bioelectricity production from a phytoplankton, Chlorella vulgaris, and a macrophyte, Ulva lactuca was examined in single chamber microbial fuel cells (MFCs). MFCs were fed with the two algae (as powders), obtaining differences in energy recovery, degradation efficiency, and power densities. C. vulgaris produced more energy generation per substrate mass (2.5 kWh/kg), but U. lactuca was degraded more completely over a batch cycle (73 ± 1% COD). Maximum power densities obtained using either single cycle or multiple cycle methods were 0.98 W/m2 (277 W/m3) using C. vulgaris, and 0.76 W/m2 (215 W/m3) using U. lactuca. Polarization curves obtained using a common method of linear sweep voltammetry (LSV) overestimated maximum power densities at a scan rate of 1 mV/s. At 0.1 mV/s, however, the LSV polarization data was in better agreement with single‐ and multiple‐cycle polarization curves. The fingerprints of microbial communities developed in reactors had only 11% similarity to inocula and clustered according to the type of bioprocess used. These results demonstrate that algae can in principle, be used as a renewable source of electricity production in MFCs. Biotechnol. Bioeng. 2009;103: 1068–1076.

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Xiuping Zhu

Pennsylvania State University

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Wulin Yang

Pennsylvania State University

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Weihua He

Harbin Institute of Technology

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Michael A. Hickner

Pennsylvania State University

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Yujie Feng

Harbin Institute of Technology

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John M. Regan

Pennsylvania State University

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Jia Liu

Harbin Institute of Technology

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