181 research outputs found

    Biological and microbial fuel cells

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    Biological fuel cells have attracted increasing interest in recent years because of their applications in environmental treatment, energy recovery, and small-scale power sources. Biological fuel cells are capable of producing electricity in the same way as a chemical fuel cell: there is a constant supply of fuel into the anode and a constant supply of oxidant into the cathode; however, typically the fuel is a hydrocarbon compound present in the wastewater, for example. Microbial fuel cells (MFCs) are also a promising technology for efficient wastewater treatment and generating energy as direct electricity for onsite remote application. MFCs are obtained when catalyst layer used into classical fuel cells (polymer electrolyte fuel cell) is replaced with electrogenic bacteria. A particular case of biological fuel cell is represented by enzyme-based fuel cells, when the catalyst layer is obtained by immobilization of enzyme on the electrode surface. These cells are of particular interest in biomedical research and health care and in environmental monitoring and are used as the power source for portable electronic devices. The technology developed for fabrication of enzyme electrodes is described. Different enzyme immobilization methods using layered structures with self-assembled monolayers and entrapment of enzymes in polymer matrixes are reviewed. The performances of enzymatic biofuel cells are summarized and approaches on further development to overcome current challenges are discussed. This innovative technology will have a major impact and benefit to medical science and clinical research, health care management, and energy production from renewable sources. Applications and advantages of using MFCs for wastewater treatment are described, including organic matter removal efficiency and electricity generation. Factors affecting the performance of MFC are summarized and further development needs are accentuated

    From microbial fuel cell (MFC) to microbial electrochemical snorkel (MES): maximizing chemical oxygen demand (COD) removal from wastewater

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    The paper introduces the concept of the microbial electrochemical snorkel (MES), a simplified design of a “short-circuited” microbial fuel cell (MFC). The MES cannot provide current but it is optimized for wastewater treatment. An electrochemically active biofilm (EAB) was grown on graphite felt under constant polarization in an urban wastewater. Controlling the electrode potential and inoculating the bioreactor with a suspension of an established EAB improved the performance and the reproducibility of the anodes. Anodes, colonized by an EAB were tested for the chemical oxygen demand (COD) removal from urban wastewater using a variety of bio-electrochemical processes (microbial electrolysis, MFC, MES). The MES technology, as well as a short-circuited MFC, led to a COD removal 57% higher than a 1000 Ω-connected MFC, confirming the potential for wastewater treatment

    IMPACT OF THE 1998 ICE STORM ON THE EASTERN ONTARIO MAPLE SYRUP INDUSTRY: A CASE STUDY OF NATURAL DISASTER POLICY IN CANADA

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    Under Canada's Disaster Financial Assistance Arrangements (DFAA), the federal government can provide provinces with funds for emergency response and recovery in the event of a natural disaster. This assistance has historically been provided on an ad hoc basis. In recent years, the amount of DFAA assistance has significantly increased without any auditing to determine how effective and efficient these expenditures are in offsetting economic losses due to natural disasters. The goal of this paper is to examine the implications of natural disaster compensation and assistance programs for economic efficiency. A framework is developed to determine if government assistance expenditures have offset economic losses to a specific industry using a case study of the 1998 ice storm and the eastern Ontario maple syrup industry. Projections of damage recovery are used to measure the economic impact of the storm, and a comparison is then drawn between the change in producers' welfare and government assistance. The implications of the findings for the case study and for future natural disaster assistance programs in Canada are discussed.Environmental Economics and Policy, Resource /Energy Economics and Policy,

    Non-conventional gas phase remediation of volatile halogenated compounds by dehydrated bacteria

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    Traditional biological removal processes are limited by the low solubility of halogenated compounds in aqueous media. A new technology appears very suitable for the remediation of these volatile organic compounds (VOCs). Solid/gas bio-catalysis applied in VOC remediation can transform halogenated compounds directly in the gas phase using dehydrated cells as a bio-catalyst. The hydrolysis of volatile halogenated substrates into the corresponding alcohol was studied in a solid/gas biofilter where lyophilised bacterial cultures were used as the catalyst. Four strains containing dehalogenase enzymes were tested for the hydrolysis of 1-chlorobutane. The highest removal yield was obtained using the dhaA-containing strains, the maximal reaction rate of 0.8 micromol min(-1)g(-1) being observed with Escherichia coli BL21(DE3)(dhaA). Various treatments such as cell disruption by lysozyme or alkaline gas addition in the bio-filter could stabilise the dehalogenase activity of the bacteria. A pre-treatment of the dehydrated bacterial cells by ammonia vapour improved the stability of the catalyst and a removal activity of 0.9 micromol min(-1)g(-1) was then obtained for 60h. Finally, the process was extended to a range of halogenated substrates including bromo- and chloro-substrates. It was shown that the removal capacity for long halogenated compounds (C(5)-C(6)) was greatly increased relative to traditional biological processes

    First air-tolerant effective stainless steel microbial anode obtained from a natural marine biofilm

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    Microbial anodes were constructed with stainless steel electrodes under constant polarisation. The seawater medium was inoculated with a natural biofilm scraped from harbour equipment. This procedure led to efficient microbial anodes providing up to 4 A/m2 for 10 mM acetate oxidation at −0.1 V/SCE. The whole current was due to the presence of biofilm on the electrode surface, without any significant involvement of the abiotic oxidation of sulphide or soluble metabolites. Using a natural biofilm as inoculum ensured almost optimal performance of the biofilm anode as soon as it was set up; the procedure also proved able to form biofilms in fully aerated media, which provided up to 0.7 A/m2. The current density was finally raised to 8.2 A per square meter projected surface area using a stainless steel grid. The inoculating procedure used here combined with the control of the potential revealed, for the first time, stainless steel as a very competitive material for forming bioanodes with natural microbial consortia

    Nonconventional hydrolytic dehalogenation of 1-chlorobutane by dehydrated bacteria in a continuous solid-gas biofilter

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    Rhodococcus erythropolis NCIMB 13064 and Xanthobacter autotrophicus GJ10 are able to catalyze the conversion of halogenated hydrocarbons to their corresponding alcohols. These strains are attractive biocatalysts for gas phase remediation of polluted gaseous effluents because of their complementary specificity for short or medium and for mono-, di-, or trisubstituted halogenated hydrocarbons (C2-C8 for Rhodococcus erythropolis and C1-C4 for Xanthobacter autotrophicus). After dehydration, these bacteria can catalyze the hydrolytic dehalogenation of 1-chlorobutane in a nonconventional gas phase system under a controlled water thermodynamic activity (aw). This process makes it possible to avoid the problems of solubility and bacterial development due to the presence of water in the traditional biofilters. In the aqueous phase, the dehalogenase activity of Rhodococcus erythropolis is less sensitive to thermal denaturation and the apparent Michaelis-Menten constants at 30°C were 0.4 mM and 2.40 μmol min−1 g−1 for Km and Vmax, respectively. For Xanthobacter autotrophicus they were 2.8 mM and 0.35 μmol min−1 g−1. In the gas phase, the behavior of dehydrated Xanthobacter autotrophicus cells is different from that observed with Rhododcoccus erythropolis cells. The stability of the dehalogenase activity is markedly lower. It is shown that the HCl produced during the reaction is responsible for this low stability. Contrary to Rhodococcus erythropolis cells, disruption of cell walls does not increase the stability of the dehalogenase activity. The activity and stability of lyophilized Xanthobacter autotrophicus GJ10 cells are dependant on various parameters. Optimal dehalogenase activity was determined for water thermodynamic activity (aw) of 0.85. A temperature of 30°C offers the best compromise between activity and stability. The pH control before dehydration plays a role in the ionization state of the dehalogenase in the cells. The apparent Michaelis-Menten constants Km and Vmax for the dehydrated Xanthobacter autotrophicus cells were 0.07 (1-chlorobutane thermodynamic activity) and 0.08 μmol min−1 g−1 of cells, respectively. A maximal transformation capacity of 1.4 g of 1-chlorobutane per day was finally obtained using 1g of lyophilized Xanthobacter autotrophicus GJ10 cell

    Bioremediation of halogenated compounds: comparison of dehalogenating bacteria and improvement of catalyst stability

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    Five bacterial strains were compared for halogenated compounds conversion in aqueous media. Depending on the strain, the optimal temperature for dehalogenase activity of resting cells varied from 30 to 45 degrees C, while optimal pH raised from 8.4 to 9.0. The most effective dehalogenase activity for 1 chlorobutane conversion was detected with Rhodococcus erythropolis NCIMB13064 and Escherichia coli BL21 (DE3) (DhaA). The presence of 2-chlorobutane or propanal in the aqueous media could inhibit the 1-chlorobutane transformation

    Coupled oxidation–reduction of butanol–hexanal by resting Rhodococcus erythropolis NCIMB 13064 cells in liquid and gas phases

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    Rhodococcus erythropolis is a promising Gram-positive bacterium capable of numerous bioconversions including those involving alcohol dehydrogenases (ADHs). In this work, we compared and optimized the redox biocatalytic performances of 1-butanol-grown R. erythropolis NCIMB 13064 cells in aqueous and in non-conventional gas phase using the 1-butanol–hexanal oxidation–reduction as model reaction. Oxidation of 1-butanol to butanal is tightly coupled to the reduction of hexanal to 1-hexanol at the level of a nicotinoprotein–ADH-like enzyme. Cell viability is dispensable for reaction. In aqueous batch conditions, fresh and lyophilized cells are efficient redox catalysts (oxidation–reduction rate = 76 micromol min−1 g cell dry mass−1) being also reactive towards benzyl alcohol, (S)-2-pentanol, and geraniol as reductants. However, butanol hexanal oxidation–reduction is strongly limited by product accumulation and by hexanal toxicity that is amajor factor influencing cell behavior and performance. Reaction rate is maximal at 40 ◦C pH 7.0 in aqueous phase and at 60 ◦C- pH 7.0–9.0 in gas phase. Importantly, lyophilized cells also showed to be promising redox catalysts in the gas phase (at least 65 micromol min−1 g cell dry mass−1). The system is notably stable for several days at moderate thermodynamic activities of hexanal (0.06–0.12), 1-butanol (0.12) and water (0.7)

    Election by Majority Judgement: Experimental Evidence

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    Le jugement majoritaire est une méthode d'élection. Cette méthode est l'aboutissement d'une nouvelle théorie du choix social où les électeurs jugent les candidats au lieu de les ranger. La théorie est développée dans d'autres publications ([2, 4]). Cet article décrit et analyse des expériences électorales conduites pendant les deux dernières élections présidentielles françaises dans plusieurs buts: (1) démontrer que le jugement majoritaire est une méthode pratique, (2) la décrire et établir ses principales propriétés, (3) démontrer qu'elle échappe aux paradoxes classiques, et (4) illustrer comment dans la pratique tous les mécanismes de vote connus violent certains critères importants. Les démonstrations utilisent des concepts et méthodes nouveaux.

    Biodeterioration of cementitious materials in biogas digester

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    In biogas production plants, concrete structures suffer chemical and biological attacks during the anaerobic digestion process. The attack on concrete may be linked to the effects of (i) organic acids; (ii) ammonium and CO2 co-produced by the microorganisms’ metabolisms; and (iii) the bacteria’s ability to form biofilms on the concrete surface. In a context of biogas industry expansion, the mechanisms of concrete deterioration need to be better understood in order to propose innovative, efficient solutions. This study aims, firstly, to characterise the evolution of the biochemical composition of the biodegradable wastes during digestion so as to identify the compounds that are aggressive for concrete. Secondly, it aims to evaluate the mechanisms of concrete deterioration in anaerobic digesters. CEM I paste specimens were immersed in synthetic inoculated biowaste in anaerobic digestion conditions. The liquid fractions were analysed chemically. The alteration mechanisms of the cementitious matrices were investigated using XRD and SEM analyses. The maximal total concentration of organic acids was 65 mmol/L in the liquid fraction during the digestion process. The pH evolution showed two phases: acidification in the first few days and then a slow increase to pH 7–8. In only 4 weeks, an abundant biofilm developed on the cement paste surface. Biodeterioration leads to calcium leaching and carbonation of the cement past
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