Marc Verhaege

Biofuel Cells Select for Microbial Consortia That Self-Mediate Electron Transfer

ABSTRACT Microbial fuel cells hold great promise as a sustainable biotechnological solution to future energy needs. Current efforts to improve the efficiency of such fuel cells are limited by the lack of knowledge about the microbial ecology of these systems. The purposes of this study were (i) to elucidate whether a bacterial community, either suspended or attached to an electrode, can evolve in a microbial fuel cell to bring about higher power output, and (ii) to identify species responsible for the electricity generation. Enrichment by repeated transfer of a bacterial consortium harvested from the anode compartment of a biofuel cell in which glucose was used increased the output from an initial level of 0.6 W m−2 of electrode surface to a maximal level of 4.31 W m−2 (664 mV, 30.9 mA) when plain graphite electrodes were used. This result was obtained with an average loading rate of 1 g of glucose liter−1 day−1 and corresponded to 81% efficiency for electron transfer from glucose to electricity. Cyclic voltammetry indicated that the enhanced microbial consortium had either membrane-bound or excreted redox components that were not initially detected in the community. Dominant species of the enhanced culture were identified by denaturing gradient gel electrophoresis and culturing. The community consisted mainly of facultative anaerobic bacteria, such as Alcaligenes faecalis and Enterococcus gallinarum, which are capable of hydrogen production. Pseudomonas aeruginosa and other Pseudomonas species were also isolated. For several isolates, electrochemical activity was mainly due to excreted redox mediators, and one of these mediators, pyocyanin produced by P. aeruginosa, could be characterized. Overall, the enrichment procedure, irrespective of whether only attached or suspended bacteria were examined, selected for organisms capable of mediating the electron transfer either by direct bacterial transfer or by excretion of redox components.

Electrochemical degradation of surfactants by intermediates of water discharge at carbon-based electrodes

The electrochemical oxidation of anionic (sodium dodecylbenzenesulfonate) and cationic (hexadecyltrimethyl ammonium chloride) aqueous dilute surfactant solutions at a BDD (boron-doped diamond) electrode has been studied by batch electrolysis experiments and potentiodynamic measurements. In the potential region of water decomposition (E>2.3 V vs. SHE), surfactants could be deactivated and oxidised with total organic carbon (TOC) removals up to 82% by the action of intermediates of water discharge (e.g. hydroxyl radicals). Of the investigated process parameters, the initial electrolyte pH had the highest impact on surfactant oxidation. An initial pH of 10 significantly enhanced the electrochemical oxidation of both surfactants. The process was not diffusion-controlled and instantaneous current efficiencies (ICE) for TOC removal were in all cases low, varying from 5 to 12% on average. The surfactant deactivation and oxidation potential of the BDD electrode was compared with other carbon-based electrodes. Applying an equal electrode surface, the BDD electrode showed much higher surfactant removals compared to plane graphite. Graphite granules and carbon felt suffered from abrasion, leading to additional carbon loading of the surfactant solutions. Based on the current electrolysis configuration, the specific energy requirement with the BDD electrode for the electrochemical oxidation of surfactants was estimated at 10–20 kW h m−3 effective wastewater.

Indirect electrochemical oxidation of reverse osmosis membrane concentrates at boron-doped diamond electrodes

The treatment or disposal of concentrates generated from the filtrative treatment of water is rapidly becoming a factor of major environmental concern. This preliminary study discusses a novel approach in the abatement of reverse osmosis membrane retentate i.e. electrochemical oxidation. The recalcitrant organic constituents as well as the ammonia nitrogen in the retentate could be readily oxidised using boron-doped diamond electrodes. From the model fitted to these data, a constant removal rate and current efficiency was calculated. Analysis of the inorganic chlorinated species revealed that the oxidation mechanism was mainly due to the indirect oxidative action of electrogenerated hypochlorite.

On the methodology of Thermal Desorption Spectroscopy to evaluate hydrogen embrittlement

Thermal desorption spectroscopy (TDS) is a very important tool in hydrogen embrittlement (HE) related research and has been applied on many different materials over the last decades in order to improve knowledge on the HE phenomenon. TDS provides the opportunity to distinguish between different types of hydrogen traps based on the analysis of a spectrum with different peak temperatures each corresponding to hydrogen desorption from a specific trap. These peak temperatures, and consequently the different traps in a material, arise from the various microstructural characteristics of the material. However, TDS results are also influenced by many other parameters, such as the sample surface preparation, the electrolytes used for hydrogen charging, sample geometry, charging time, current density, charging temperature. Even though the use of thermal desorption to evaluate hydrogen-metal interactions has increased over the past years, a careful evaluation of the effect of these other parameters was not yet performed. In this work, the impact of some of the above mentioned parameters was studied. It was demonstrated that the sample geometry, the surface roughness, and the initial total pressure of the TDS chamber influenced significantly the obtained TDS spectrum.

Corrosion properties of nickel free austenitic stainless steels in 0.5M H2SO4 and 0.5M H2SO4 plus 0.4M NaCl

Abstract The corrosion behaviour of four nickel free austenitic stainless steels were investigated in 0·5M H2SO4 and 0·5M H2SO4 plus 0·4M NaCl solutions by means of potentiodynamic and potentiostatic anodic polarisation testing. The performances of the nickel free alloys are compared to those of an experimental intermediate nickel alloy (4%Ni) and a standard AISI 304 steel grade. Once passivity was reached all alloys displayed similar current densities i p in 0·5M H2SO4, independent from alloying. Mo and Cu were shown to be beneficial in decreasing the active dissolution currents and i crit values. The commercial AISI 304 steel displayed superior resistance to pit initiation during potentiodynamic testing, and AISI 304 steel displayed the highest E pit value of all alloys tested. When tested potentiostatically the N and Mo alloyed nickel free alloys showed excellent resistance to pit initiation and growth. The dominant effect of N was associated with repassivation of incipient pits, while Mo appeared to act at an earlier stage, suppressing initiation.