TY - JOUR
T1 - Influence of the preparation process on the performance of three hydrotalcite-based De-SOx catalysts
AU - Kong, Jiechen
AU - Jiang, Lei
AU - Huo, Zhiping
AU - Xu, Xiangyu
AU - Evans, David G.
AU - Song, Jiaqing
AU - He, Mingyuan
AU - Li, Zhaofei
AU - Wang, Qian
AU - Yan, Lijun
PY - 2013
Y1 - 2013
N2 - In this study, three hydrotalcite-based De-SOx catalysts were prepared using different approaches: impregnation, coprecipitation, and precipitation using the separate nucleation and aging steps (SNAS) method. The physicochemical properties of these catalysts were studied and their SOx removal behaviors were characterized with a custom-built apparatus simulating the conditions in a fluid catalytic cracking (FCC) regenerator. The results showed that the catalyst prepared using the SNAS method had the highest SOx adsorption rate, the largest SOx pick-up capacity (1.31 g/g cat.) and the lowest onset reduction temperature (805 K), which makes it an excellent De-SOx catalyst with promising applications in industry.
AB - In this study, three hydrotalcite-based De-SOx catalysts were prepared using different approaches: impregnation, coprecipitation, and precipitation using the separate nucleation and aging steps (SNAS) method. The physicochemical properties of these catalysts were studied and their SOx removal behaviors were characterized with a custom-built apparatus simulating the conditions in a fluid catalytic cracking (FCC) regenerator. The results showed that the catalyst prepared using the SNAS method had the highest SOx adsorption rate, the largest SOx pick-up capacity (1.31 g/g cat.) and the lowest onset reduction temperature (805 K), which makes it an excellent De-SOx catalyst with promising applications in industry.
KW - Ce/MgAl mixed oxides
KW - Reduction temperature
KW - SNAS
UR - https://www.scopus.com/pages/publications/84879475228
U2 - 10.1016/j.catcom.2013.05.026
DO - 10.1016/j.catcom.2013.05.026
M3 - Article
AN - SCOPUS:84879475228
SN - 1566-7367
VL - 40
SP - 59
EP - 62
JO - Catalysis Communications
JF - Catalysis Communications
ER -