Publications by authors named "Marc Cretin"

Per-and polyfluoroalkyl substances (PFAS), known as "forever chemicals", are posing a considerable threat to human health and the environment, that conventional treatment methods are unable to treat. In recent years, electrochemical advanced oxidation emerged as a promising technology for the degradation of recalcitrant pollutants such as PFAS. This work reports the degradation of perfluorooctanoic acid (PFOA) and perfluorooctanesulfonic acid (PFOS), using a Magnéli phase-based anode type TiO by electro-oxidation and electro-oxidation combined with electro-Fenton.

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Advanced oxidation processes are the most efficient tool to thwart the overaccumulation of harmful organic compounds in the environment. In this direction bioinspired metal complexes may be a viable solution for oxidative degradations in water. However, their synthesis is often elaborated and their scalability consequently low.

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It has become necessary to develop effective strategies to prevent and reduce water pollution as a result of the increase in dangerous pollutants in water reservoirs. Consequently, there is a need to design new catalyst materials to promote the efficiency of advanced oxidation processes (AOPs) in the field of wastewater treatment plant to ensure the mineralization of trace organic contaminants. A notable approach gaining attention involves the coupling of sulfate radicals-based AOPs to photocatalysis or electrocatalysis processes, aiming to achieve the complete removal of refractory contaminants into water and carbon dioxide.

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Cellulose-based materials are a sustainable alternative to polymers derived from petroleum. Cellulose nanocrystal (CNC) is a biopolymer belonging to this family; it is commonly known for its important physical and chemical properties and ability to form a film. Modifying CNC via electrostatic interaction provided by cationic polymers is a facile and promising technique to enlarge the application of CNC.

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The many pollutants detected in water represent a global environmental issue. Emerging and persistent organic pollutants are particularly difficult to remove using traditional treatment methods. Electro-oxidation and sulfate-radical-based advanced oxidation processes are innovative removal methods for these contaminants.

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Electrodeposited bismuth ferrite (BiFeO) thin films on fluorine-doped tin oxide (FTO) substrate were employed as photoanodes in the photoelectrocatalytic degradation of methylene blue. The BiFeO thin films electrodeposited for 300 s, 600 s, 1200 s, 1800 s and 3600 s were characterised with XRD, field emission scanning electron microscopy (FESEM) and UV-vis diffuse reflectance spectroscopy. SEM images displayed different morphology at different electrodeposition times which affects the photoelectrocatalytic (PEC) performances.

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In this study, we combined electrospinning of a large amount of halloysite (HNT, 95%) with nitriding to produce N-HNT-TiO composite nanofibers (N-H95T5 hereafter) to be used for acetaminophen (ACT) photodegradation. Investigation of the morphological and structural properties of the obtained materials did not highlight any significant difference in their morphological features and confirmed that nitrogen was evenly distributed in the samples. Photocatalytic tests under visible light showed that acetaminophen photodegraded faster in the presence of samples with nitrogen (N-H95T5) than without (H95T5 nanofibers).

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The study of the adsorption efficiency of new carbon/CNT composites was undertaken to remove a cationic dye, Rhodamine B (RhB), from dye-contaminated wastewater. Indeed, we investigated the effect of different experimental parameters such as time, initial concentration of dye and temperature on the adsorption of RhB by the carbon composites (KS44-0 and KS44-20). The results showed that the adsorption uptake increased with the initial concentration and solution temperature while maintaining a relatively constant pH.

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Cellulose nanocrystal (CNC) has recently gained much attention due to its unique properties such as abundancy, biodegradability, high strength, large surface area, functional ability, template structure, and sustainability. To broaden its application and enhance its compatibility with other materials, CNC can be modified via different methods. The modification is based on introducing new functions, including esterification, silylation, carbamation, polymerization, and so on.

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Flow capacitive deionization is a water desalination technique that uses liquid carbon-based electrodes to recover fresh water from brackish or seawater. This is a potential second-generation water desalination process, however it is limited by parameters such as feed electrode conductivity, interfacial resistance, viscosity, and so on. In this study, titanium oxide nanofibers (TiONF) were manufactured using an electrospinning process and then blended with commercial activated carbon (AC) to create a well distributed flow electrode in this study.

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We developed free-standing nitrogen-doped carbon nanofiber (CNF) electrodes incorporating Co/CoO nanoparticles (NPs) as a new cathode material for removing Acid Orange 7 (AO7; a dye for wool) from wastewater by the heterogeneous electro-Fenton reaction. We produced the free-standing N-doped CNF electrodes by electrospinning a polyacrylonitrile (PAN) and cobalt acetate solution followed by thermal carbonation of the cobalt acetate/PAN nanofibers under a nitrogen atmosphere. We then investigated electro-Fenton-based removal of AO7 from wastewater with the free-standing N-doped-CNFs-Co/CoO electrodes, in the presence or not of Fe ions as a co-catalyst.

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The objective of this work was to evaluate obtaining LiOH directly from brines with high LiCl concentrations using bipolar membrane electrodialysis by the analysis of Li ion transport phenomena. For this purpose, Neosepta BP and Fumasep FBM bipolar membranes were characterized by linear sweep voltammetry, and the Li transport number in cation-exchange membranes was determined. In addition, a laboratory-scale reactor was designed, constructed, and tested to develop experimental LiOH production tests.

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In recent years, electrochemical methods utilizing reactive electrochemical membranes (REM) have been recognized as the most promising technologies for the removal of organic pollutants from water. In this paper, we propose a 1D convection-diffusion-reaction model concerning the transport and oxidation of oxalic acid () and oxygen evolution in the flow-through electrochemical oxidation system with REM. It allows the determination of unknown parameters of the system by treatment of experimental data and predicts the behavior of the electrolysis setup.

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The use of reactive electrochemical membranes (REM) in flow-through mode during the anodic oxidation of organic compounds makes it possible to overcome the limitations of plate anodes: in the case of REM, the area of the electrochemically active surface is several orders of magnitude larger, and the delivery of organic compounds to the reaction zone is controlled by convective flow rather than diffusion. The main problem with REM is the formation of fouling and gas bubbles in the pores, which leads to a decrease in the efficiency of the process because the hydraulic resistance increases and the electrochemically active surface is shielded. This work aims to study the processes underlying the reduction in the efficiency of anodic oxidation, and in particular the formation of gas bubbles and the recharge of the REM pore surface at a current density exceeding the limiting kinetic value.

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Capacitive deionization is a second-generation water desalination technology in which porous electrodes (activated carbon materials) are used to temporarily store ions. In this technology, porous carbon used as electrodes have inherent limitations, such as low electrical conductivity, low capacitance, etc., and, as such, optimization of electrode materials by rational design to obtain hybrid electrodes is key towards improvement in desalination performance.

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Capacitive deionization is an emerging brackish water desalination technology whose principle lies in the utilization of porous electrodes (activated carbon materials) to temporarily store ions. Improving the properties of carbon material used as electrodes have been the focus of recent research, as this is beneficial for overall efficiency of this technology. Herein, we have synthesized a composite of activated carbon/graphene oxide electrodes by using a simple blending process in order to improve the hydrophilic property of activated carbon.

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Electro-oxidation of acetaminophen (ACT) in three different doped secondary effluents collected from a conventional Municipal Waste Water Treatment Plant (MWWTP), a MWWTP using a membrane bioreactor (WWTP MBR) and a lab-scale MBR treating source-separated urine (Urine MBR) was investigated by electro-Fenton (EF) coupled with anodic oxidation (AO) using sub-stoichiometric titanium oxide anode (TiO). After 8 h of treatment, 90 ± 15%, 76 ± 3.8% and 46 ± 1.

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In recent years, electrochemical methods utilizing reactive electrochemical membranes (REM) have been considered as a promising technology for efficient degradation and mineralization of organic compounds in natural, industrial and municipal wastewaters. In this paper, we propose a two-dimensional (2D) convection-diffusion-reaction model concerning the transport and reaction of organic species with hydroxyl radicals generated at a TiO REM operated in flow-through mode. It allows the determination of unknown parameters of the system by treatment of experimental data and predicts the behavior of the electrolysis setup.

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Electrochemical water desalination has been a major research area since the 1960s with the development of capacitive deionization technique. For the latter, its modus operandi lies in temporary salt ion adsorption when a simple potential difference (1.0-1.

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The traditional electro-Fenton (EF) has been facing major challenges including narrow suitable range of pH and non-reusability of catalyst. To overcome these drawbacks we synthesized FeFe-layered double hydroxide modified carbon felt (FeFe LDH-CF) cathode via in situ solvo-thermal process. Chemical composition and electrochemical characterization of FeFe LDH-CF were tested and analyzed.

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In the recent years, polyborate anions have been considered as possible candidates for energy. In aqueous solutions, they have been studied as either hydrogen carriers or anodic fuels. In the solid state (as an alkali salt), they have been seen as solid electrolytes.

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The objective of this study was to implement electrochemical advanced oxidation processes (EAOPs) for mineralization and biodegradability enhancement of nanofiltration (NF) concentrate from landfill leachate initially pre-treated in a membrane bioreactor (MBR). Raw carbon felt (CF) or FeFe layered double hydroxides-modified CF were used for comparing the efficiency of homogeneous and heterogeneous electro-Fenton (EF), respectively. The highest mineralization rate was obtained by heterogeneous EF: 96% removal of dissolved organic carbon (DOC) was achieved after 8 h of electrolysis at circumneutral initial pH (pH = 7.

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Catalytic electrodes were prepared via carbonization of MIL-53(Fe) on the surface of porous carbon felt electrodes (CF) for use in wastewater treatment by the heterogeneous electro-Fenton (EF) process. The best results were obtained when the carbon felt was pretreated with nitric acid, enhancing the affinity of the MIL-53(Fe) for the surface. Following a series of optimization experiments, carbonization conditions of 800 °C for 5 h were used to form Fe-nanoporous carbon (MOFs@CF).

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Article Synopsis
  • Electro-oxidation processes offer a promising way to remove organic pollutants from water without needing chemical reagents, but they face challenges like slow mass transfer that limits efficiency for large-scale use.
  • Recent breakthroughs like reactive electrochemical membranes (REMs) improve performance by enhancing the electrochemically active surface area and speeding up the mass transport of pollutants.
  • Advancements in materials, particularly sub-stoichiometric titanium oxide REMs, show promise due to their high electrical conductivity, reactivity, stability, and effective mass transport properties, aiming for better electrodes for electro-oxidation.
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Reactive Electrochemical Membrane (REM) prepared from carbothermal reduction of TiO is used for the mineralization of biorefractory pollutants during filtration operation. The mixture of TiO and TiO Magnéli phases ensures the high reactivity of the membrane for organic compound oxidation through OH mediated oxidation and direct electron transfer. In cross-flow filtration mode, convection-enhanced mass transport of pollutants can be achieved from the high membrane permeability (3300 LMH bar).

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