Published December 30, 2016 | Version v1
Journal article

Synthesis and characterization of pure and (Ce, Zr, Ag) doped mesoporous CuO-Fe2O3 as highly efficient and stable nanocatalysts for CO oxidation at low temperature

Description

Highlights: • Highly active and stable Fe-Cu mixed oxides were prepared by co-precipitation method. • Addition of CuO to Fe2O3 increases the chemisorbed oxygen, the conductivity and SBET. • Activation energy of CO oxidation significantly decreased via doping with foreign ions. - Abstract: A series of single and mixed oxide nanocatalysts of mesoporous CuO-Fe2O3 with different CuO contents (1–50 wt.%) were prepared by a co-precipitation method and further promoted by trace amounts of CeO2, ZrO2 and Ag2O (0.1–0.5 wt.%) dopants. The original and calcined catalysts were characterized by TG, DTA, XRD, TEM, VSM, N2 sorption analysis, surface chemisorbed oxygen and DC electrical conductivity measurements. The catalytic performance of these nanocatalysts toward CO oxidation was studied using a conventional fixed bed flow type reactor. The results revealed that the addition of 1–20 wt.% CuO to Fe2O3 monotonically increases the specific surface area, the amount of surface chemisorbed oxygen, electrical conductivity and catalytic activity of the nanocatalysts. In addition, the catalytic activity indicated that Fe-Cu mixed oxide nanocatalyst promoted with the three dopants (CeO2, ZrO2 and Ag2O) exhibited the highest catalytic activity with a total conversion of CO into CO2 at 100 °C. Moreover, the activation energy of CO oxidation decreased from 38.4 to 23.1 kJmol−1 upon treating the catalyst containing 20 wt.% CuO with the three dopants. Finally the effects of various operational parameters were also studied.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.apsusc.2016.08.114

Additional details

Identifiers

DOI
10.1016/j.apsusc.2016.08.114;
PII
S0169-4332(16)31757-3;

Publishing Information

Journal Title
Applied Surface Science
Journal Volume
390
Journal Page Range
p. 649-665
ISSN
0169-4332
CODEN
ASUSEE

Optional Information

Copyright
Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.