TY - JOUR
T1 - Synergetic removal of elemental mercury and NO over TiCe 0.25 Sn 0.25 O x catalysts from flue gas
T2 - Performance and mechanism study
AU - Yang, Bo
AU - Li, Zhong
AU - Huang, Qiong
AU - Chen, Mindong
AU - Xu, Leilei
AU - Shen, Yuesong
AU - Zhu, Shemin
N1 - Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2019/3/15
Y1 - 2019/3/15
N2 - A novel TiCe 0.25 Sn 0.25 O x catalyst was designed and prepared by a sol-gel method for synergetic removal of NO and elemental mercury (Hg 0 ) from flue gas. The as-designed TiCe 0.25 Sn 0.25 O x catalyst achieved a synergetic removal efficiency of NO (NH 3 -SCR) and Hg 0 (Hg 0 oxidation) of 95%, 85% and 70%, 65% (after 300 ppm SO 2 and 6 vol% H 2 O were injected) at 200 °C under simulated flue gases conditions, respectively. Moreover, the mercury, which gathered on the surface of TiCe 0.25 Sn 0.25 O x after adsorption and oxidation, could be released and collected by the thermal decomposition method, avoiding the secondary pollution by mercury. The mechanism underlying the synergetic removal of NO and Hg 0 was also investigated using various characterization techniques. The synergistic catalysis between redox and solid acid contributed to the synergetic removal of NO and Hg 0 over TiCe 0.25 Sn 0.25 O x . The results of XRD and XPS revealed that the lattice oxygen was a key factor for Hg 0 oxidation reaction. The results of N 2 -physisorption, NH 3 -TPD, H 2 -TPR and Py-IR illustrated that TiCe 0.25 Sn 0.25 O x possessed the mesopores structure, suitable particle sizes, the excellent redox and weak acid (Lewis sites) properties, contributing to its high NO and Hg 0 removal efficiency. Furthermore, the removal of NO and Hg 0 showed a synergetic effect. The analysis of Hg-TPD and (NO + O 2 )-TPD had confirmed that the mid-product NO 2 of NH 3 -SCR reaction was favorable for Hg 0 oxidation. In summary, the TiCe 0.25 Sn 0.25 O x possesses not only good synergetic removal performance for NO and Hg 0 but also satisfactory anti-sulfur performance, which is a promising candidate for the effective and economical removal of NO and Hg 0 in the cement and steel industries.
AB - A novel TiCe 0.25 Sn 0.25 O x catalyst was designed and prepared by a sol-gel method for synergetic removal of NO and elemental mercury (Hg 0 ) from flue gas. The as-designed TiCe 0.25 Sn 0.25 O x catalyst achieved a synergetic removal efficiency of NO (NH 3 -SCR) and Hg 0 (Hg 0 oxidation) of 95%, 85% and 70%, 65% (after 300 ppm SO 2 and 6 vol% H 2 O were injected) at 200 °C under simulated flue gases conditions, respectively. Moreover, the mercury, which gathered on the surface of TiCe 0.25 Sn 0.25 O x after adsorption and oxidation, could be released and collected by the thermal decomposition method, avoiding the secondary pollution by mercury. The mechanism underlying the synergetic removal of NO and Hg 0 was also investigated using various characterization techniques. The synergistic catalysis between redox and solid acid contributed to the synergetic removal of NO and Hg 0 over TiCe 0.25 Sn 0.25 O x . The results of XRD and XPS revealed that the lattice oxygen was a key factor for Hg 0 oxidation reaction. The results of N 2 -physisorption, NH 3 -TPD, H 2 -TPR and Py-IR illustrated that TiCe 0.25 Sn 0.25 O x possessed the mesopores structure, suitable particle sizes, the excellent redox and weak acid (Lewis sites) properties, contributing to its high NO and Hg 0 removal efficiency. Furthermore, the removal of NO and Hg 0 showed a synergetic effect. The analysis of Hg-TPD and (NO + O 2 )-TPD had confirmed that the mid-product NO 2 of NH 3 -SCR reaction was favorable for Hg 0 oxidation. In summary, the TiCe 0.25 Sn 0.25 O x possesses not only good synergetic removal performance for NO and Hg 0 but also satisfactory anti-sulfur performance, which is a promising candidate for the effective and economical removal of NO and Hg 0 in the cement and steel industries.
KW - Elemental mercury (Hg )
KW - Low temperatures
KW - Nitrogen oxides (NO )
KW - Removal mechanism
KW - Synergetic removal
UR - http://www.scopus.com/inward/record.url?scp=85054015194&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2018.09.193
DO - 10.1016/j.cej.2018.09.193
M3 - 文章
AN - SCOPUS:85054015194
SN - 1385-8947
SP - 990
EP - 1002
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
ER -