TY - JOUR
T1 - Insight into SO2 poisoning and regeneration of one-pot synthesized Cu-SSZ-13 catalyst for selective reduction of NOx by NH3
AU - Yong, Xin
AU - Chen, Hong
AU - Zhao, Huawang
AU - Wei, Miao
AU - Zhao, Yingnan
AU - Li, Yongdan
N1 - Publisher Copyright:
© 2021 The Chemical Industry and Engineering Society of China, and Chemical Industry Press Co., Ltd
PY - 2022/6
Y1 - 2022/6
N2 - The effects of SO2 on an one-pot synthesized Cu-SSZ-13 catalyst for selective reduction of NOx by NH3 were examined. The addition of SO2 inhibited NOx conversion significantly below 300 °C, while no effect on NOx conversion was observed above 300 °C. TGA, TPD, and XPS results showed that the deactivation was caused by the formation of (NH4)2SO4, SO2 chemisorption on the isolated Cu2+ ion sites, as well as the formation of CuSO4-like species. Among them, the site-blocking effect of (NH4)2SO4 on Cu2+ was the primary reason for deactivation. Fortunately, 89% of deNOx activity of the poisoned catalyst was recovered after thermal treatment at 500 °C in air, where (NH4)2SO4 was completely decomposed. The activity was further recovered with regeneration temperature increasing to 600 °C, removing the adsorbed SO2 on the Cu2+ sites. The regeneration at 600 °C could not recover the activity completely, because of the high stability of CuSO4-like species.
AB - The effects of SO2 on an one-pot synthesized Cu-SSZ-13 catalyst for selective reduction of NOx by NH3 were examined. The addition of SO2 inhibited NOx conversion significantly below 300 °C, while no effect on NOx conversion was observed above 300 °C. TGA, TPD, and XPS results showed that the deactivation was caused by the formation of (NH4)2SO4, SO2 chemisorption on the isolated Cu2+ ion sites, as well as the formation of CuSO4-like species. Among them, the site-blocking effect of (NH4)2SO4 on Cu2+ was the primary reason for deactivation. Fortunately, 89% of deNOx activity of the poisoned catalyst was recovered after thermal treatment at 500 °C in air, where (NH4)2SO4 was completely decomposed. The activity was further recovered with regeneration temperature increasing to 600 °C, removing the adsorbed SO2 on the Cu2+ sites. The regeneration at 600 °C could not recover the activity completely, because of the high stability of CuSO4-like species.
KW - Activity regeneration
KW - Emission control
KW - One-pot synthesis of Cu-SSZ-13
KW - SCR
KW - SO poisoning
UR - http://www.scopus.com/inward/record.url?scp=85130103345&partnerID=8YFLogxK
U2 - 10.1016/j.cjche.2021.06.012
DO - 10.1016/j.cjche.2021.06.012
M3 - Article
AN - SCOPUS:85130103345
SN - 1004-9541
VL - 46
SP - 184
EP - 193
JO - Chinese Journal of Chemical Engineering
JF - Chinese Journal of Chemical Engineering
ER -