Effective degradation of aqueous carbamazepine on a novel blue-colored TiO2 nanotube arrays membrane filter anode
- 1. Research Center for Eco-Environmental Engineering, Dongguan University of Technology, Dongguan, 523808 (China)
- 2. Key Laboratory of Industrial Ecology and Environmental Engineering, Ministry of Education, School of Environmental and Technology, Dalian University of Technology, Dalian, 116023 (China)
- 3. School of Environmental Science and Engineering, Shaanxi University of Science and Technology, Xi'an, 710021 (China)
- 4. Brook Byers Institute of Sustainable Systems, School of Civil and Environmental Engineering, Georgia Institute of Technology, Atlanta, GA, 30332 (United States)
Description
Highlights: • Novel BC-TiO2NTA membrane filter electrode is developed. • Electrochemical oxidation of carbamazepine in aqueous solution is investigated. • Electrochemical degradation of carbamazepine follows pseudo-first-order reaction kinetics. • Possible electrochemical degradation mechanisms of carbamazepine are proposed. The effective electrochemical oxidation of aqueous carbamazepine (CBZ) using a novel blue-colored TiO2 nanotube arrays (BC-TiO2NTA) membrane filter anode was studied. The BC-TiO2NTA was characterized using SEM, TEM, BET, mercury intrusion porosimetry, XPS, XRD, CV, and LSV. The BC-TiO2NTA had reserved pore structure, formed mesopores, specific and electroactive surface areas of 2.01 m2 g−1 and 9.32 cm2 cm−2, respectively. The oxygen evolution potential was 2.61 V vs. SCE. CBZ could be degraded by OH, SO4− and O2− on BC-TiO2NTA in accordance to pseudo-first-order kinetic, which was greatly enhanced in flow-through mode. The optimal kinetic rate constant of CBZ degradation of 0.403 min−1 was achieved at 3 mA cm−2, while energy consumption per order was 0.086 kW h m−3. The mineralization efficiency and mineralization current efficiency were 50.8 % and 9.5 % at 180 min, respectively. The presence of Cl− (0.3−3 mM) accelerated electrochemical degradation of CBZ, while NO3− (0.1−2 mM) inhibited the reaction. Based on density functional theory calculation and UPLC-Orbitrap-MS/MS measurement, we found that electrochemical degradation of CBZ was initialized by cleavage of −CONH2 group and attack of OH on the olefinic double bond of the central heterocyclic ring.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jhazmat.2020.123530Additional details
Identifiers
- DOI
- 10.1016/j.jhazmat.2020.123530;
- PII
- S0304389420315168;
Publishing Information
- Journal Title
- Journal of Hazardous Materials
- Journal Volume
- 402
- Journal Page Range
- vp.
- ISSN
- 0304-3894
- CODEN
- JHMAD9
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 54051683
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; S46: INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND TECHNOLOGY;
- Descriptors DEI
- ANODES; AQUEOUS SOLUTIONS; CHLORINE IONS; DENSITY FUNCTIONAL METHOD; ELECTROCHEMISTRY; ENERGY CONSUMPTION; NANOTUBES; NITRATES; OXIDATION; PORE STRUCTURE; REACTION KINETICS; SCANNING ELECTRON MICROSCOPY; SURFACE AREA; TITANIUM OXIDES; TRANSMISSION ELECTRON MICROSCOPY; WATER INFLUX; X-RAY DIFFRACTION; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- CALCULATION METHODS; CHALCOGENIDES; CHARGED PARTICLES; CHEMICAL REACTIONS; CHEMISTRY; COHERENT SCATTERING; DIFFRACTION; DISPERSIONS; ELECTRODES; ELECTRON MICROSCOPY; ELECTRON SPECTROSCOPY; HOMOGENEOUS MIXTURES; IONS; KINETICS; MICROSCOPY; MICROSTRUCTURE; MIXTURES; NANOSTRUCTURES; NITROGEN COMPOUNDS; OXIDES; OXYGEN COMPOUNDS; PHOTOELECTRON SPECTROSCOPY; SCATTERING; SOLUTIONS; SPECTROSCOPY; SURFACE PROPERTIES; TITANIUM COMPOUNDS; TRANSITION ELEMENT COMPOUNDS; VARIATIONAL METHODS
Optional Information
- Copyright
- Copyright (c) 2020 Elsevier B.V. All rights reserved.