4.8 Article

Fabrication of novel SnO2-Sb/carbon aerogel electrode for ultrasonic electrochemical oxidation of perfluorooctanoate with high catalytic efficiency

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 136, Issue -, Pages 278-286

Publisher

ELSEVIER
DOI: 10.1016/j.apcatb.2013.02.013

Keywords

Sb-doped SnO2; Carbon aerogel electrode; Electrochemical oxidation; Ultrasonic irradiation; Perfluorooctanoate

Funding

  1. National Natural Science Foundation P.R. China [21077077, 21207101]
  2. Shanghai Municipal Education Commission
  3. Shanghai Educational Development Foundation [2011CG19]
  4. Program for Young Excellent Talents in Tongji University [2010KJ063]

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A novel SnO2-Sb/CA electrode, possessing high surface area, strong adsorption capacity, good electrical conductivity and electrocatalytic activity, was firstly proposed for ultrasonic electrochemical oxidation (US-EC) of persistent high concentration perfluorooctanoate (PFOA) in this study. The optimal calcination temperature for sinking micro-sized SnO2-Sb particles existed on the surface of CA into the structure of CA as nanoparticles was 600 degrees C. Its application on degrading PFOA (60 mL of 100 mg L-1) exhibited efficient electrocatalytic performance. After 5 h electrolysis, over 91% of PFOA was degraded with a first-order kinetic constant of 0.52 h(-1) and over 86% TOC removal was achieved, while 47% PFOA removal and 33% TOC removal were obtained in traditional electrochemical (EC) process. The main role of determining the decomposition efficiency, i.e., the mass transport, hydroxyl radical (center dot OH) generation and electrode surface reaction, were greatly enhanced in US-EC system. Additionally, the generated intermediates existing on electrode surface and in solution were separately detected after different electrolysis time and the proper mechanism for efficient removing PFOA in US-EC process was investigated in detail. At early reaction stage (<0.511), the intermediate products on SnO2-Sb/CA surface were C5F11COO-, C4F9COO-, C3F7COO-, C2F5COO-, CF3COO-, while in solution were C5F11COO-, (C4FCOO-)-C-9, C3F7COO-. At late reaction stage (>5 h), the intermediates either on electrode surface or in solution became the same including C5F11COO-, C4F9COO-, C3F7COO-. (C) 2013 Elsevier B.V. All rights reserved.

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