Published January 2021 | Version v1
Journal article

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.2020.123530

Additional 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

Optional Information

Copyright
Copyright (c) 2020 Elsevier B.V. All rights reserved.