TY - JOUR
T1 - Performance of K-promoted hydrotalcite-derived CoMgAlO catalysts used for soot combustion, NOx storage and simultaneous soot-NOx removal
AU - Li, Qian
AU - Meng, Ming
AU - Tsubaki, Noritatsu
AU - Li, Xingang
AU - Li, Zhaoqiang
AU - Xie, Yaning
AU - Hu, Tiandou
AU - Zhang, Jing
N1 - Funding Information:
This work is financially supported by the National Natural Science Foundation of China (No. 20876110, No. 20676097), the “863” Programs of the Ministry of Science and Technology of China (No. 2008AA06Z323, No. 2006AA06Z348) and the Program of New Century Excellent Talents in University of China (NCET-07-0599). The authors are also grateful to the Natural Science Foundation of Tianjin (No. 07JCYBJC15100), the Cheung Kong Scholar Program for Innovative Teams of the Ministry of Education (No. IRT0641) and the Program of Introducing Talents of Discipline to University of China (No. B06006).
PY - 2009/9/7
Y1 - 2009/9/7
N2 - A series of K-promoted hydrotalcite-derived CoMgAlO catalysts were synthesized by coprecipitation. Their catalytic performance for soot combustion, NOx storage and simultaneous soot-NOx removal was evaluated, respectively. The techniques of TG/DTA, BET, XRD, EXAFS, XPS and in situ DRIFTS were employed for catalyst characterization. When K is added to the catalyst CoMgAlO, soot combustion is largely accelerated, with the temperature (Tm) for maximum soot conversion lowered by at least 50 °C. Moreover, the NOx reduction by soot over the catalysts calcined at 500-700 °C is also facilitated. The K-containing catalyst calcined at 600 °C shows not only the highest soot combustion rate, but also the maximum NOx reduction percentage of 32%, which is attributed to its high surface K/Co atomic ratio and the strong interaction between K and Co. In situ DRIFTS results reveal that NO is readily oxidized to NO2 and stored as nitrates over K-promoted catalysts, which could be reduced by soot more efficiently. Based on these investigations, a reaction pathway for soot combustion, NOx storage and simultaneous soot-NOx removal is proposed.
AB - A series of K-promoted hydrotalcite-derived CoMgAlO catalysts were synthesized by coprecipitation. Their catalytic performance for soot combustion, NOx storage and simultaneous soot-NOx removal was evaluated, respectively. The techniques of TG/DTA, BET, XRD, EXAFS, XPS and in situ DRIFTS were employed for catalyst characterization. When K is added to the catalyst CoMgAlO, soot combustion is largely accelerated, with the temperature (Tm) for maximum soot conversion lowered by at least 50 °C. Moreover, the NOx reduction by soot over the catalysts calcined at 500-700 °C is also facilitated. The K-containing catalyst calcined at 600 °C shows not only the highest soot combustion rate, but also the maximum NOx reduction percentage of 32%, which is attributed to its high surface K/Co atomic ratio and the strong interaction between K and Co. In situ DRIFTS results reveal that NO is readily oxidized to NO2 and stored as nitrates over K-promoted catalysts, which could be reduced by soot more efficiently. Based on these investigations, a reaction pathway for soot combustion, NOx storage and simultaneous soot-NOx removal is proposed.
KW - Calcination temperature
KW - Hydrotalcite-derived CoMgAlO catalysts
KW - NOx
KW - Potassium
KW - Soot
UR - http://www.scopus.com/inward/record.url?scp=67651177834&partnerID=8YFLogxK
U2 - 10.1016/j.apcatb.2009.06.007
DO - 10.1016/j.apcatb.2009.06.007
M3 - 学術論文
AN - SCOPUS:67651177834
SN - 0926-3373
VL - 91
SP - 406
EP - 415
JO - Applied Catalysis B: Environmental
JF - Applied Catalysis B: Environmental
IS - 1-2
ER -