Publications by authors named "Couvert Annabelle"

One of the technical barriers to the wider use of biochar in the composting practices is the lack of accurate quantification linking biochar properties to application outcomes. To address this issue, this paper investigates the use of ammonia nitrogen adsorption capacity by biochar as a predictor of ammonia emission during composting in the presence of biochar. With this in mind, this work investigated the use of ammonia nitrogen adsorption capacity of biochar when mixed with solid digestate, and the reduction in ammonia emissions resulting from the addition of biochar during aerobic degradation of solid digestate.

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The fast-growing consumer demand drives industrial process intensification, which subsequently creates a significant amount of waste. These products are discharged into the environment and can affect the quality of air, degrade water streams, and alter soil characteristics. Waste materials may contain polluting agents that are especially harmful to human health and the ecosystem, such as the synthetic dyes, phenolic agents, polycyclic aromatic hydrocarbons, volatile organic compounds, polychlorinated biphenyls, pesticides and drug substances.

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This work aimed at presenting a green method using a new source of peroxidase isolated from Raphanus sativus var. niger (RSVNP) in immobilized form, for the treatment of wastewater. To ensure stability and enzymatic activity in the biodegradation process, RSVNP was immobilized as a cross-linked enzyme aggregate (CLEAs).

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This study aimed to evaluate the global patterns of odor generation and odorant composition for different operational stages of anaerobically digested sewage sludge (ADS) composting at pilot scale. To this end, gas emissions were sampled and analyzed during storage, forced aeration treatment (active phase), turning process and curing. For each operational stage, odors were monitored by measuring the odor emission rates (OER in OU h kgADS) through dynamic olfactometry and computing the odor activity values (OAVs) of compounds quantified by analytical methods (i.

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Hazardous and odorous gas emissions from composting and methanization plants are an issue of public concern. Odor and chemical monitoring are thus critical steps in providing suitable strategies for air pollution control at waste treatment units. In this study, 141 gas samples were extensively analyzed to characterize the odor and chemical emissions released upon the aerobic treatment of 10 raw substrates and five digestates.

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Peroxidase from Brassica rapa was immobilized as cross-linked enzyme aggregates (CLEAs) and used to treat air containing phenol as a model molecule of volatile organic compounds (VOCs). Prior to an enzymatic treatment, phenol was absorbed into an aqueous or organic phase (silicone oil) to reach concentrations ranging from 20 to 160 mg/L. The process was carried out by introducing a desired weighing of BRP-CLEAs into preparations and reaction was started by injecting HO solution to the medium.

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Three volatile organic compounds (VOC) with no acidic or basic function (butanol, butyraldehyde, methylethylketone), encountered at low concentrations in odorous effluents, were absorbed in water in a compact wet scrubber. This gas-liquid contactor consisted of a wire mesh packing structure where the gas phase flows at high velocity (>12 m s). A very turbulent two-phase downward flow could be observed in the scrubber with dispersed fine droplets (around 10 μm).

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This study proposes a new technique to treat waste air containing 2-Chlorophenol (2-CP), namely an integrated process coupling absorption of the compound in an organic liquid phase and its enzymatic degradation. Silicone oil (47V20) was used as an organic absorbent to allow the volatile organic compound (VOC) transfer from the gas phase to the liquid phase followed by its degradation by means of Cross-linked Brassica rapa peroxidase (BRP) contained in the organic phase. An evaluation of silicone oil (47V20) absorption capacity towards 2-CP was first accomplished by determining its partition coefficient (H) in this solvent.

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Synthesis of several hydrophobic ionic liquids (ILs), which might be selected as good candidates for degradation of hydrophobic volatile organic compounds in a two-phase partitioning bioreactor (TPPB), were carried out. Several bioassays were also realized, such as toxicity evaluation on activated sludge and zebrafish, cytotoxicity, fluoride release in aqueous phase and biodegradability in order to verify their possible effects in case of discharge in the aquatic environment and/or human contact during industrial manipulation. The synthesized compounds consist of alkylimidazoliums, functionalized imidazoliums, isoqinoliniums, triazoliums, sulfoniums, pyrrolidiniums and morpholiniums and various counter-ions such as: PF6(-), NTf2(-) and NfO(-).

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Removal of high concentrations of hydrogen sulfide using a biofilter packed with expanded schist under extreme acidic conditions was performed. The impact of various parameters such as H2S concentration, pH changes and sulfate accumulation on the performances of the process was evaluated. Elimination efficiency decreased when the pH was lower than 1 and the sulfate accumulation was more than 12 mg S-SO4(2-)/g dry media, due to a continuous overloading by high H2S concentrations.

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Enzymatic discoloration of the diazo dye, Congo red (CR), by immobilized plant peroxidase from turnip "Brassica rapa" is investigated. Partially purified turnip peroxidase (TP) was immobilized by entrapment in spherical particles of calcium alginate and was assayed for the discoloration of aqueous CR solution. Experimental data revealed that pH, reaction time, temperature, colorant, and H2O2 concentration play a significant role in dye degradation.

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In this work, a simulation tool was developed for hydrogen sulphide (H₂S) removal in an alkaline solution in packed columns working at countercurrent. Modelling takes into account the mass-transfer enhancement due to the reversible reactions between H₂S and the alkaline species (CO(²⁻)(3), HCO⁻(3), and HO⁻) in the liquid film. Many parameters can be controlled by the user such as the gas and liquid inlet H₂S concentrations, the gas and liquid flow rates, the scrubbing liquid pH, the desired H₂S removal efficiency, the temperature, the alkalinity, etc.

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A solid/liquid system involving activated sludge immobilized in an agar medium and a non-aqueous phase liquid containing the target pollutant has been considered to treat a model hydrophobic volatile organic compound, toluene. The positive impact of the use of a multiphase bioreactor is that the organic phase constitutes a pollutant reservoir and also helps to overcome possible pollutant toxicity. In addition and to overcome the drawbacks of the use of a solid organic phase (high pressure drop and low mass transfer) instead of a liquid organic phase, the considered solid phase was the aqueous.

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A two-phase partitioning bioreactor was considered to remove toluene contained in a biodegradable organic phase by activated sludge (AS). The selected solvent was hexadecane. In a first step, the biodegradation of toluene dissolved in hexadecane by AS was examined.

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A wide range of siloxanes exist but the most abundant in biogas are Hexamethyldisiloxane (L2) and Octamethyltrisiloxane (L3) as linear siloxanes and Octamethylcyclotetrasiloxane (D4) as a cyclic siloxane. In order to remove volatile organic compound from biogas, different processes can be used. A promising process for siloxane removal is their absorption in an organic solvent.

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The enzyme peroxidase is known for its capacity to remove phenolic compounds and aromatic amines from aqueous solutions and also to decolourize textile effluents. This study aims at evaluating the potential of a turnip (Brassica rapa) peroxidase (TP) preparation in the discolouration of textile azo dyes and effluents. An azo dye, Congo Red (CR), was used as a model pollutant for treatment by the enzyme.

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This study assesses the potential of ozonation and advanced oxidation process O(3)/H(2)O(2) to enhance the dimethyldisulfide (DMDS) mass transfer in a compact chemical scrubber developed for air treatment applications. Theoretical calculations, through Hatta number and enhancement factor evaluations for two parallel irreversible reactions, were compared to experimental data and enabled the description of the mass transfer mechanisms. These calculations required the determination of the kinetic constant of the DMDS oxidation by molecular ozone ( [Formula: see text] ) and the measurement of the hydroxyl radical concentration within the scrubber.

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Ionic liquids (ILs) constitute a new generation of solvents entirely composed of ions. ILs are usually considered as green solvents due to their negligible vapor pressure and other properties, such as non-flammability and high thermostability. Biotechnological applications involving the use of ILs are currently emerging.

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A lab-scale pilot plant was developed in order to measure the efficiency of some odour-neutralizing products for the removal of odorous compounds. Experiments were carried out on gas and liquid flows in two configurations: co-current and counter-current, which differ in the values of the drop diameter and the contact time, leading to different behaviours between highly water-soluble compounds like ammonia and other compounds like sulphurous compounds. Mass transfer was shown to be modified by the presence of neutralizing products as a result of their pH and surface tension.

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More stringent legislation on dissolved organic matter (DOM) urges the drinking water industry to improve in DOM removal, especially when applied to water with high dissolved organic carbon (DOC) contents and low turbidity. To improve conventional processes currently used in drinking water treatment plants (DWTPs), the performances of a hybrid membrane bioreactor containing fluidized activated carbon were investigated at the DWTP of Rennes. Preliminary results showed that the residual DOC was the major part of the non-biodegradable fraction.

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Dimethyl disulphide (DMDS) removal was investigated in a compact scrubber (hydraulic residence time approximately 20ms), composed of a wire mesh packing structure where liquid and gas flow at co-current and high gas superficial velocity (>12m s(-1)). In order to regenerate the scrubbing liquid and to maintain a driving force in the scrubber, ozone and hydrogen peroxide were added to water since they allow the generation of nonselective and highly reactive species, hydroxyl radicals HO(). Three ways of reagent distribution were tested.

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To slow down the hydrogen peroxide decomposition in basic aqueous conditions, the addition of stabilizers and co-stabilizers in the scrubbing solution was investigated. Results found with sodium silicate (Na2SiO3) were quite promising but several problems still remained. Based on these observations, this study focused on the research of a better stabilizer.

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