4.6 Article

Preparation and electrochemical property of TiO2/Nano-graphite composite anode for electro-catalytic degradation of ceftriaxone sodium

Journal

ELECTROCHIMICA ACTA
Volume 180, Issue -, Pages 957-964

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2015.09.055

Keywords

Electrochemical property; Anode material; Nano-graphite (Nano-G); Anodic oxidation

Funding

  1. National Natural Science Foundation of China for Youth [21106035]
  2. Youth Scholar Backbone Supporting Plan Project for General Colleges and Universities of Heilongjiang province [1151G034]
  3. Key Laboratory of Chemical Engineering Process & Technology for High-efficiency Conversion

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Titanium dioxide/Nano-graphite (TiO2/Nano-G) composite was synthesized by a sol-gel method and TiO2/Nano-G electrode was prepared in hot-press approach. The composite was characterized by X-ray photoelectron spectroscopy (XPS), fourier transform infrared (FT-IR), scanning electrons microscopy (SEM), transmission electron microscopy (TEM) and X-ray diffraction (XRD). The electrochemical performance of the TiO2/Nano-G anode electrode was investigated through cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The electro-catalytic performance was evaluated by the yield of (OH)-O-center dot radicals, degradation of methyl orange and ceftriaxone sodium. The results demonstrated that TiO2 nanoparticles were dispersed on the surface and interlamination of the Nano-G uniformly, TiO2/Nano-G electrode owned higher electro-catalytic oxidation activity and stability than Nano-G electrode. Degradation rate of ceftriaxone sodium within 120 min by TiO2(40)/Nano-G electrode was 97.7%. And (OH)-O-center dot radicals given by TiO2/Nano-G electrode was higher than that of Nano-G electrode and DSA (Ti/IrO2-RuO2) electrode. The excellent electro-catalytic performance could be ascribed to the admirable conductive property of the Nano-G and more production of (OH)-O-center dot offered by TiO2(40)/Nano-G electrode. (C) 2015 Elsevier Ltd. All rights reserved.

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