TY - JOUR
T1 - Promoting effect of Nb doping on NH3-SCR of NOx at high temperature over Zr5W1Ox
AU - Wang, Shouli
AU - Shen, Yuesong
N1 - Publisher Copyright:
© 2025 Elsevier Ltd
PY - 2025/8/15
Y1 - 2025/8/15
N2 - Driven by the strategy of reducing pollution and CO2 emissions, high-temperature deNOx has become a major demand for NOx treatment of gas exhaust such as gas power generation. This paper intends to further improve the high-temperature deNOx performance of Zr5W1Ox by Nb doping. A series of Zr5W1NbaOx with different Nb contents were synthesized by sol–gel method for NH3-SCR of NO. Combined with characterization analysis of FE-SEM, XRD, XPS, N2 adsorption–desorption, H2-TPR, NH3-TPD and in situ DRIFTS, the influence mechanism of Nb incorporation was discussed. The results showed that the addition of Nb promoted the deNOx activity temperature window of the catalyst to shift towards high temperature by 30 ℃. Among them, Zr5W1Nb0.09Ox exhibited better high-temperature NH3-SCR deNOx activity, and its efficiency of NH3-SCR of NO reached over 90 % within 480–683 ℃ at a space velocity of 50000 h−1; Moreover, under the coexistence of 5 vol% water vapor and 200 ppm SO2, its deNOx activity did not decrease, exhibiting excellent resistance to water vapor and SO2 poisoning. Analysis showed that there were both Lewis and Brønsted acid sites on the surface of Zr5W1Nb0.09Ox. The addition of Nb increased the strength of the medium and strong acid sites of the catalyst, enhanced its effective adsorption of NH3 molecules, and broadened the high-temperature deNOx activity temperature window. in situ DRIFTS analysis confirmed that the high-temperature NH3-SCR deNOx reaction of Zr5W1Nb0.09Ox followed both Eley-Rideal and Langmuir-Hinshelwood mechanisms.
AB - Driven by the strategy of reducing pollution and CO2 emissions, high-temperature deNOx has become a major demand for NOx treatment of gas exhaust such as gas power generation. This paper intends to further improve the high-temperature deNOx performance of Zr5W1Ox by Nb doping. A series of Zr5W1NbaOx with different Nb contents were synthesized by sol–gel method for NH3-SCR of NO. Combined with characterization analysis of FE-SEM, XRD, XPS, N2 adsorption–desorption, H2-TPR, NH3-TPD and in situ DRIFTS, the influence mechanism of Nb incorporation was discussed. The results showed that the addition of Nb promoted the deNOx activity temperature window of the catalyst to shift towards high temperature by 30 ℃. Among them, Zr5W1Nb0.09Ox exhibited better high-temperature NH3-SCR deNOx activity, and its efficiency of NH3-SCR of NO reached over 90 % within 480–683 ℃ at a space velocity of 50000 h−1; Moreover, under the coexistence of 5 vol% water vapor and 200 ppm SO2, its deNOx activity did not decrease, exhibiting excellent resistance to water vapor and SO2 poisoning. Analysis showed that there were both Lewis and Brønsted acid sites on the surface of Zr5W1Nb0.09Ox. The addition of Nb increased the strength of the medium and strong acid sites of the catalyst, enhanced its effective adsorption of NH3 molecules, and broadened the high-temperature deNOx activity temperature window. in situ DRIFTS analysis confirmed that the high-temperature NH3-SCR deNOx reaction of Zr5W1Nb0.09Ox followed both Eley-Rideal and Langmuir-Hinshelwood mechanisms.
KW - High-temperature deNO
KW - Nb doping
KW - NH-SCR
KW - Promoting effect
KW - ZrWO
UR - http://www.scopus.com/inward/record.url?scp=105000232016&partnerID=8YFLogxK
U2 - 10.1016/j.fuel.2025.135137
DO - 10.1016/j.fuel.2025.135137
M3 - 文章
AN - SCOPUS:105000232016
SN - 0016-2361
VL - 394
JO - Fuel
JF - Fuel
M1 - 135137
ER -