TY - JOUR
T1 - The transient reduction of NO with CO and naphthalene in the presence of oxygen using a core-shell SmCeO2@TiO2-supported copper catalyst
AU - Venegas, Fernanda
AU - López, Naima
AU - Sánchez-Calderón, Luis
AU - Aguila, Gonzalo
AU - Araya, Paulo
AU - Guo, Xuyun
AU - Zhu, Ye
AU - Guerrero, Sichem
N1 - Funding Information:
Funding from the Chilean National Commission for Scientific and Technological Research (CONICYT) is gratefully acknowledged (FONDECYT Regular 1160721 and FONDEF IDeA ID16I10358). TEM work was carried out at the Hong Kong Polytechnic University and was supported by the Hong Kong Research Grants Council through the Early Career Scheme (Project 25301617) and the Hong Kong Polytechnic University grant (Project 1-ZE6G). Dr. X. Guo and Dr. Y. Zhu thank Dr. Wei Lu for optimizing the JEOL JEM-2100F microscope.
Publisher Copyright:
© 2019 The Royal Society of Chemistry.
PY - 2019
Y1 - 2019
N2 - This work studied the reaction of common pollutants on a catalytic surface under oxidizing conditions. CO and naphthalene were used to reduce NO in the presence of oxygen during the transient heating of metal oxide nanoparticles. The latter consisted of a core-shell SmCeO2@TiO2 support with a TiO2 core and a samarium-stabilized CeO2 shell, impregnated with copper and potassium. The addition of potassium simulated the gradual accumulation of an alkali metal during biomass combustion, which can poison the catalyst. The Cu/SmCeO2@TiO2 catalyst achieved the complete conversions of NO, CO and naphthalene at 225, 236 and 255 °C, respectively. Even though the inclusion of potassium had the expected negative effect, the K/Cu/SmCeO2@TiO2 catalyst was still able to fully convert NO and CO at 323 and 299 °C, respectively, whereas a maximum naphthalene conversion of only 66% was obtained at 350 °C.
AB - This work studied the reaction of common pollutants on a catalytic surface under oxidizing conditions. CO and naphthalene were used to reduce NO in the presence of oxygen during the transient heating of metal oxide nanoparticles. The latter consisted of a core-shell SmCeO2@TiO2 support with a TiO2 core and a samarium-stabilized CeO2 shell, impregnated with copper and potassium. The addition of potassium simulated the gradual accumulation of an alkali metal during biomass combustion, which can poison the catalyst. The Cu/SmCeO2@TiO2 catalyst achieved the complete conversions of NO, CO and naphthalene at 225, 236 and 255 °C, respectively. Even though the inclusion of potassium had the expected negative effect, the K/Cu/SmCeO2@TiO2 catalyst was still able to fully convert NO and CO at 323 and 299 °C, respectively, whereas a maximum naphthalene conversion of only 66% was obtained at 350 °C.
UR - http://www.scopus.com/inward/record.url?scp=85068471850&partnerID=8YFLogxK
U2 - 10.1039/c9cy00545e
DO - 10.1039/c9cy00545e
M3 - Article
AN - SCOPUS:85068471850
SN - 2044-4753
VL - 9
SP - 3408
EP - 3415
JO - Catalysis Science and Technology
JF - Catalysis Science and Technology
IS - 13
ER -