TY - JOUR
T1 - Enhancement of Low-Temperature Catalytic Activity over a Highly Dispersed Fe-Mn/Ti Catalyst for Selective Catalytic Reduction of NOx with NH3
AU - Mu, Jincheng
AU - Li, Xinyong
AU - Sun, Wenbo
AU - Fan, Shiying
AU - Wang, Xinyang
AU - Wang, Liang
AU - Qin, Meichun
AU - Gan, Guoqiang
AU - Yin, Zhifan
AU - Zhang, Dongke
PY - 2018/8/8
Y1 - 2018/8/8
N2 - A novel Fe2O3-MnO2/TiO2 catalyst was synthesized using a conventional impregnation method assisted with ethylene glycol and used for NH3-SCR. The catalyst exhibited superior low-temperature activity over a broad temperature window (100-325 °C), low apparent activation energy, and excellent sulfur-poisoning resistance. The characterization results revealed that the catalyst was greatly dispersed with smaller particles, and the partial doping of Fe into the TiO2 lattice thereby led to the formation of the Fe-O-Ti structure, which could strengthen the electronic inductive effect and increase the ratio of surface chemisorption oxygen, resulting in the enhancement of NO oxidation and favoring the low-temperature SCR activity via a "fast SCR" process. The in situ FTIR analysis showed that the NOx adsorption capacity was significantly improved due to the desired dispersion property, further helping both the SCR activity and reaction rate at low temperatures. The present work confirmed that more active sites can be provided on the catalyst surface by modifying the dispersity.
AB - A novel Fe2O3-MnO2/TiO2 catalyst was synthesized using a conventional impregnation method assisted with ethylene glycol and used for NH3-SCR. The catalyst exhibited superior low-temperature activity over a broad temperature window (100-325 °C), low apparent activation energy, and excellent sulfur-poisoning resistance. The characterization results revealed that the catalyst was greatly dispersed with smaller particles, and the partial doping of Fe into the TiO2 lattice thereby led to the formation of the Fe-O-Ti structure, which could strengthen the electronic inductive effect and increase the ratio of surface chemisorption oxygen, resulting in the enhancement of NO oxidation and favoring the low-temperature SCR activity via a "fast SCR" process. The in situ FTIR analysis showed that the NOx adsorption capacity was significantly improved due to the desired dispersion property, further helping both the SCR activity and reaction rate at low temperatures. The present work confirmed that more active sites can be provided on the catalyst surface by modifying the dispersity.
UR - http://www.scopus.com/inward/record.url?scp=85049687042&partnerID=8YFLogxK
U2 - 10.1021/acs.iecr.8b01335
DO - 10.1021/acs.iecr.8b01335
M3 - Article
AN - SCOPUS:85049687042
SN - 0888-5885
VL - 57
SP - 10159
EP - 10169
JO - Industrial and Engineering Chemistry Research
JF - Industrial and Engineering Chemistry Research
IS - 31
ER -