TY - JOUR
T1 - Highly active and stable VOx/TiO2 nanosheets for low-temperature NH3-SCR of NO
T2 - Structure-directing role of support
AU - Lin, Liang Yi
AU - Wang, Yu Chen
AU - Liu, Zi Lan
N1 - Publisher Copyright:
© 2024 Elsevier B.V.
PY - 2024/3/15
Y1 - 2024/3/15
N2 - Low-temperature NH3-SCR over conventional catalysts based on V2O5/TiO2 is significantly limited by the narrow range of operating temperatures and poor activity at low temperatures. Herein, a novel catalyst consisting of defective TiO2 nanosheets supported vanadia (V/TNS) is successfully developed for the low-temperature NH3-SCR of NO. The V/TNS catalyst demonstrated excellent SCR performance, achieving over 95 % conversion with high N2 selectivity (>90 %) over a wide temperature range of 140–380 °C. Importantly, V/TNS was highly resistant to H2O and SO2 poisoning during 30 h of continuous operation, maintaining an NO conversion efficiency that exceeded 92 % at 180 °C. In contrast, a high-surface-area anatase TiO2 particle-supported catalyst (V/TiO2(A)) suffered from catalytic deactivation. Detailed characterization revealed that the TNS support, with its abundant surface defects and high surface area, improved vanadia dispersion and facilitated the formation of surface V4+ species and oxygen vacancies. These factors synergistically enhanced the adsorption and activation of NH3 and NOx, boosting catalytic performance. Moreover, the presence of SO2 had a notable inhibitory effect on the adsorption and activation of NH3 and NOx and their reactions on V/TiO2(A), while these detrimental effects were considerably mitigated on V/TNS.
AB - Low-temperature NH3-SCR over conventional catalysts based on V2O5/TiO2 is significantly limited by the narrow range of operating temperatures and poor activity at low temperatures. Herein, a novel catalyst consisting of defective TiO2 nanosheets supported vanadia (V/TNS) is successfully developed for the low-temperature NH3-SCR of NO. The V/TNS catalyst demonstrated excellent SCR performance, achieving over 95 % conversion with high N2 selectivity (>90 %) over a wide temperature range of 140–380 °C. Importantly, V/TNS was highly resistant to H2O and SO2 poisoning during 30 h of continuous operation, maintaining an NO conversion efficiency that exceeded 92 % at 180 °C. In contrast, a high-surface-area anatase TiO2 particle-supported catalyst (V/TiO2(A)) suffered from catalytic deactivation. Detailed characterization revealed that the TNS support, with its abundant surface defects and high surface area, improved vanadia dispersion and facilitated the formation of surface V4+ species and oxygen vacancies. These factors synergistically enhanced the adsorption and activation of NH3 and NOx, boosting catalytic performance. Moreover, the presence of SO2 had a notable inhibitory effect on the adsorption and activation of NH3 and NOx and their reactions on V/TiO2(A), while these detrimental effects were considerably mitigated on V/TNS.
KW - Low coordinative sites
KW - low-temperature NH-SCR
KW - SO resistance
KW - TiO nanosheet
KW - VO/TiO
UR - http://www.scopus.com/inward/record.url?scp=85187251620&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2024.149637
DO - 10.1016/j.cej.2024.149637
M3 - Article
AN - SCOPUS:85187251620
SN - 1385-8947
VL - 484
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 149637
ER -