4.4 Article

Kinetic Approach by Photocurrent Measurements to the Photoelectrocatalytic Oxidation of an Anionic Surfactant Using an S,N-TiO2/Ti Electrode: Distinguishing Between Direct and Indirect Mechanisms

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TOPICS IN CATALYSIS
卷 64, 期 1-2, 页码 26-35

出版社

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11244-020-01404-x

关键词

Photoelectrochemical degradation; TiO2 based photoanode; Langmuir-Hinshelwood kinetic models; Direct interfacial hole transfer; Photoinduced hydroxyl radical oxidation

资金

  1. Universidad Industrial de Santander-UIS
  2. Instituto Colombiano del Petroleo-ICP, ECOPETROL (Convenio Marco de Cooperacion Tecnologica y Cientifica UIS-ECOPETROL S.A.) [5222395]
  3. COLCIENCIAS [647-2014]

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The photoelectrocatalytic oxidation of an anionic surfactant in synthetic oilfield wastewater using a S,N-TiO2/Ti electrode was studied. Results showed that at high IOS concentrations, IOS adsorption played a main role, while at low concentrations, both IOS adsorption and H2O adsorption were important for the oxidation process.
The photoelectrocatalytic oxidation of an anionic surfactant (internal olefin sulfonate C20-C24, IOS) in synthetic oilfield wastewater was investigated by photocurrent measurements using a sulfur and nitrogen co-doped titanium dioxide electrode (S,N-TiO2/Ti). For the electrode preparation, S,N-TiO2 films were supported on Ti expanded meshes by sol-gel dip-coating, followed by thermal treatment at 400 degrees C. Photocurrent measurements were performed by linear sweep voltammetry (LSV) under UV-Vis irradiation using different IOS concentrations (20-200 ppm). The photocurrent values obtained at 0.5 V vs Ag/AgCl (i(ph)) for each IOS concentration (C-IOS) were used to plot the 1/i(ph) vs 1/C-IOS graph, in which two trends were identified. For high IOS concentrations (70-200 ppm), the values fitted well to the unimolecular Langmuir-Hinshelwood (LH1) kinetic model (R-2 = 0.973), which can be associated with the direct oxidation mechanism. For low IOS concentrations (20-70 ppm), the values fitted better to a linear combination of both unimolecular and bimolecular Langmuir-Hinshelwood (LH1 and LH2) kinetic models (R-2 = 0.854), which can be associated with direct and indirect oxidation mechanisms, respectively. These results suggest that at high IOS concentrations the IOS adsorption plays the main role on the photoelectrocatalytic oxidation, while at low IOS concentrations both IOS adsorption and H2O adsorption (surface hydrophilicity) play important roles on the photoelectrocatalytic oxidation.

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