Publications by authors named "Mehmet A Oturan"

Article Synopsis
  • A new bifunctional carbon felt cathode modified with reduced graphene oxide and iron oxide (rGO-FeO/CF) was created to generate hydroxyl radicals on-site, eliminating the need for external catalysts.
  • The study focused on degrading the cytostatic drug cytarabine using two setups: the bifunctional cathode and a combination of a graphene-modified cathode with a magnetic heterogeneous Fenton catalyst.
  • Results showed that the rGO-FeO/CF system could completely degrade 0.1 mM cytarabine in 18 minutes, achieving 98.2% mineralization after 4 hours, while the rGO/CF and CNT-FeO setup reached complete degradation in just
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As an electrochemical advanced oxidation process, the electro-Fenton (EF) process has gained significant importance in the treatment of wastewater and persistent organic pollutants in recent years. As recently reported in a bibliometric analysis, the number of scientific publications on EF have increased exponentially since 2002, reaching nearly 500 articles published in 2022 (Deng et al., 2022).

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The rapid and efficient mineralization of the chemotherapeutic drug busulfan (BSF) as the target pollutant has been investigated for the first time by three different heterogeneous EF systems that were constructed to ensure the continuous electro-generation of HO and OH consisting of: i) a multifunctional carbon felt (CF) based cathode composed of reduced graphene oxide (rGO), iron oxide nanoparticles and carbon black (CB) (rGO-FeO/CB@CF), ii) rGO modified cathode (rGO/CB@CF) and rGO supported FeO (rGO-FeO) catalyst and iii) rGO modified cathode (rGO/CB@CF) and multi walled carbon nanotube supported FeO (MWCNT-FeO) catalyst. The effects of main variables, including the catalyst amount, applied current and initial pH were investigated. Based on the results, HO was produced by oxygen reduction reaction (ORR) on the liquid-solid interface of both fabricated cathodes.

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This study aimed at understanding the influence of the generation of oxidants in a heterogeneous way at boron-doped diamond (BDD) anode (anodic oxidation (AO)) or homogeneously in the bulk (electro-Fenton (EF)) during treatment of a textile industry wastewater. Both processes achieved high TOC removal. A yield of 95 % was obtained by combining EF with BDD anode during 6 h of treatment.

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This study aims to compare the efficiency of anodic oxidation with electrogenerated HO (AO-HO), electro-Fenton (EF), and their association with UV irradiation (photo anodic oxidation (PAO), and photo electro-Fenton (PEF) for the removal of Direct Red 23 from wastewater using a BDD/carbon felt cell in chloride and sulfate medium and in their combination. The effect of the supporting electrolyte was investigated in AO-HO and EF processes. High discoloration efficiency was obtained in chloride media while a higher mineralization rate was achieved in sulfate media.

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This study investigated the degradation of the antineoplastic agent 5-fluorouracil (5-FU) widely applied to treat different cancers using different advanced oxidation processes such as electro-Fenton (EF), photocatalysis with TiO and HO-modified subcritical water oxidation. The treatment with the EF process was the most efficient compared to others. Interestingly, in the EF process, the oxidative degradation of 5-FU behaved differently depending on the anode used.

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A simple, sensitive, and rapid spectrofluorimetric method was developed for the determination of the β-blocker pindolol. The native fluorescence of pindolol was measured in different organic solvents and in cyclodextrin aqueous media. The highest fluorescence signal was obtained in 2-propanol at λ = 303 nm with λ = 260 nm.

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Low yields of HO and a narrow range of appropriate pH values have been two major drawbacks for electro-Fenton (EF) process. Herein, metal-free electrochemical advanced oxidation processes (EAOPs) were developed with nitrogen and sulfur co-doped electrochemically exfoliated graphene (N, S-EEGr) electrocatalysts, which was confirmed as an outstanding bifunctional catalyst for synchronous generation and activation of HO via (2 + 1) e consecutive reduction reactions. Specifically, two elements (N, S) in metal-free N, S-EEGr-CF cathode synergize to promote the formation of HO followed by its activation.

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A lot of soil (particularly, former industrial and military sites) has been contaminated by various highly toxic contaminants such as petroleum hydrocarbons, polycyclic aromatic hydrocarbons (PAHs), polychlorobiphenyls (PCBs) or chlorinated solvents. Soil remediation is now required for their promotion into new industrial or real estate activities. Therefore, the soil washing (SW) process enhanced by the use of extracting agents (EAs) such as surfactants or cyclodextrins (CDs) has been developed for the removal of hydrophobic organic compounds (HOCs) from contaminated soils.

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Combination of the electro-Fenton process with a post-biological treatment could represent a cost-effective solution for application of electrochemical advanced oxidation processes. The objective of this study was to assess this treatment strategy in the case of a complex pharmaceutical mixture. First, main operating parameters ([Fe] and current) of the electro-Fenton process were optimized.

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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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Sequential soil washing and electrochemical advanced oxidation processes (EAOPs) were applied for the remediation of synthetic soil contaminated with diesel. The surfactant Tween 80 was used to enhance the extraction of diesel from synthetic soil, and diesel extraction efficiency was improved with the increase of Tween 80 concentration. Under conditions of 180 min washing time, 10 g synthetic soil with 100 mL surfactant solution and two times of soil washing, about 75.

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The removal of the analgesic tramadol (TMD) from water was studied by electro-Fenton (EF) process using BDD anode. Hydroxyl radicals (OH) generated in this process are very strong oxidants and able to successfully oxidize TMD until its total mineralization in aqueous solution. The oxidative degradation of TMD was very rapid with complete disappearance of 0.

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Oxidative degradation and mineralization of the antifungal drug Nystatin (NYS) was investigated using photochemical advanced oxidation processes UV-C irradiation (280-100 nm), HO photolysis (UV/HO), and photo-Fenton (UV/HO/Fe). The effect of operating parameters such as [HO], [Fe], and [NYS] initial concentrations on degradation efficiency and mineralization ability of different processes was comparatively examined in order to optimize the processes. Photo-Fenton was found to be the most efficient process attaining complete degradation of 0.

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To develop conducting organic polymers (COPs) as luminescent sensors for determination of toxic heavy metals, a new benzene sulfonic acid-doped polypyrrole (PPy-BSA) thin film was electrochemically prepared by cyclic voltammetry (CV) on flexible indium tin oxide (ITO) electrode in aqueous solution. PPy-BSA film was characterized by FTIR spectrometry, X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM). The optical properties of PPy-BSA were investigated by ultraviolet (UV)-visible absorption and fluorescence spectrometry in dimethylsulfoxide (DMSO) diluted solutions.

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Diflubenzuron (DFB) and fenuron (FEN) are benzoylurea and phenylurea pesticides, widely used in Senegal, that do not exhibit any natural fluorescence, but can be determined by means of photoinduced fluorescence (PIF) methods. Photodegradation of DFB and FEN yielded a number of fluorescent and non-fluorescent photoproducts. For both pesticides, at least 10 photoproducts were detected and identified by gas chromatography-mass spectrometry (GC/MS).

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The detoxification process mediated by carboxylic acids (CAs) has received considerable spotlights since CAs are clean reagent and ubiquitous in the natural environments and effluents. Here, we present an exhaustive review on surface-bound/dissolved metals-catalyzed Cr(VI) reduction by CAs and CAs-mediated Cr(VI) reduction by many highly/poorly reductive reagents. The overall mechanisms of Cr(VI) reduction are mainly associated with the coordination of CAs with surface-bound/dissolved metals or Cr(VI,V,IV) species and the electron donating abilities of CAs.

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An electro-Fenton (EF) based technology using activated carbon (AC) fiber as cathode and BDD as anode has been investigated for both regeneration of AC and mineralization of organic pollutants. The large specific surface area and low intraparticle diffusion resistance of AC tissue resulted in high maximum adsorption capacity of phenol (PH) (3.7 mmol g) and fast adsorption kinetics.

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Adhesively bonded polypyrrole thin films doped with benzene sulfonic acid (BSA) were electrodeposited on aminobenzenediazonium-modified flexible ITO electrodes and further employed for the detection of Pb, Cu, and Cd metal ions in aqueous medium. The aminophenyl (AP) adhesive layer was grafted to ITO by electroreduction of the in situ generated parent diazonium compound. Polypyrrole (PPy) thin films exhibited remarkable adhesion to aminophenyl (ITO-AP).

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The degradation of the herbicide fenuron was investigated using a new porous bifunctional electrode where the electrooxidation takes place on one side and the photocatalysis on the other side. The characterization of the synthetized bifunctional electrode (PbO/SnO-SbO/Ti//Ti/TiO) was performed by scanning electron microscopy, energy dispersive X-ray spectrometry and X-ray diffraction analysis and showed that the anodic side (Ti/SnO-SbO/PbO) is covered with a tetragonal β-PbO film and that the photocatalytic side (Ti/TiO) consists of an anatase phase of TiO. The single application of electrooxidation achieved 87.

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The effective removal of recalcitrant organochlorine pesticides including hexachlorocyclohexane (HCH) present in a real groundwater coming from a landfill of an old lindane (γ-HCH) factory was performed by electrochemical oxidation using a BDD anode and a carbon felt cathode. Groundwater (ΣHCHs = 0.42 mg L, TOC = 9 mg L, pH = 7, conductivity = 3.

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This study focuses on the effect of electrode materials on abatement of lindane (an organochlorine pesticide) by electrooxidation process. Comparative performances of different anodic (platinum (Pt), dimensionally stable anode (DSA) and boron-doped diamond (BDD)) and cathodic (carbon sponge (CS), carbon felt (CF) and stainless steel (SS)) materials on lindane electrooxidation and mineralization were investigated. Special attention was paid to determine the role of chlorine active species during the electrooxidation process.

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This study is focused on the effective removal of recalcitrant pollutants hexaclorocyclohexanes (HCHs, isomers α, β, γ, and δ) and chlorobenzenes (CBs) present in a real groundwater coming from a landfill of an old lindane factory. Groundwater is characterized by a total organic carbon (TOC) content of 9 mg L, pH = 7, conductivity = 3.7 mS cm, high salt concentration (SO, HCO, Cl), and ferrous iron in solution.

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Wastewater containing dyes are one of the major threats to our environment. Conventional methods are insufficient for the removal of these persistent organic pollutants. Recently much attention has been received for the oxidative removal of various organic pollutants by electrochemically generated hydroxyl radical.

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