4.6 Article

Investigation of electrocatalytic activity of nanostructure Ce-doped MnOx sol-gel coating deposited on porous Ti membrane electrode

Journal

JOURNAL OF SOL-GEL SCIENCE AND TECHNOLOGY
Volume 86, Issue 2, Pages 468-478

Publisher

SPRINGER
DOI: 10.1007/s10971-018-4620-3

Keywords

Phenolic wastewater; Ce-doped MnOx; Sol-gel; MnOx/Ti membrane electrode; Electrocatalytic membrane reactor

Funding

  1. National Natural Science Foundation of China [21676200]
  2. Program for Innovative Research Team in University of Ministry of Education of China [IRT-17R80]
  3. National key research and development plan [2016YFC0400506]

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Ce-doped MnOx/Ti electrocatalytic membrane electrodes were prepared by doping rare earth element Ce into manganese oxide (MnOx) via sol-gel method, and coated on the porous Ti substrate membrane electrode. In order to evaluate electrocatalytic activity of the Ce-MnOx/Ti electrode, a functional electrocatalytic membrane reactor (ECMR), which assembled a Ce-MnOx/Ti electrode as an anode and a stainless steel mesh as a cathode, has been employed for phenolic wastewater treatment. The results revealed that a new crystal form Ce2O3 appeared after doping Ce into the system, and the urchinlike morphology and smaller grain size of Ce-MnOx led the catalytic activity of the composite membrane electrode to improve. Moreover, the 25 mol% Ce-MnOx/Ti (C25MT) composite membrane electrode represented the best activity in the degradation of phenolic wastewater. During ECMR with C25MT operation under the conditions of 450 mg/L phenolic wastewater (500 mL), residence time of 5 min, pH of 1-13 and current density of 0.3-1.2 mA/cm(2), the highest degradation efficiency of phenolic wastewater achieved in current density of 0.9 mA/cm(2) and pH of 7, that is, the achieved remove rate of phenol, COD and TOC were 99.61, 93.12, and 84.23%, respectively. Finally, the effective reusability of C25MT composite membrane electrode was assessed, and a proposed reaction mechanism has been analyzed in the ECMR operation. [GRAPHICS] .

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