TY - JOUR
T1 - In situ treatment by high-temperature water vapor as a novel health-care approach for commercial SCR catalyst
AU - Pan, Hua
AU - Gao, Er hao
AU - Fang, Tuo tuo
AU - Mei, Yu
AU - He, Yi
AU - Shi, Yao
N1 - Publisher Copyright:
© 2020 Elsevier B.V.
PY - 2021/3/1
Y1 - 2021/3/1
N2 - Commercial selective catalytic reduction (SCR) catalysts used in a 1000 MW coal-fired power plant were in situ treated by high-temperature water vapor. The de-NOx efficiency of the deactivated catalyst increased about 25–30%, comparable to fresh commercial SCR catalysts, after being treated with simulated flue gas with 15–20 vol% high-temperature water vapor. It indicates that treatment by in situ 15–20 vol% high-temperature water vapor could significantly extend the lifetime of commercial SCR catalyst. High-temperature water vapor could remove Fe, Na, Ca, sulphate species and SiO2 depositing on SCR catalyst. Compared with the deactivated catalyst, the specific surface area, the ratio of V4+/V5+ and Lewis acid content of health-care catalyst increased from 41.679 to 44.596 m2·g−1, 1.35 to 1.80 and 45.5 to 73.8%, respectively. Density functional theory (DFT) calculation demonstrated that the electrons transferred from H2O molecule to V5+ cations in the process of H2O adsorption and the subsequent hydroxylation of V5+cations during H2O dissociation contribute to the reduction of V5+ to V4+ on the SCR catalyst.
AB - Commercial selective catalytic reduction (SCR) catalysts used in a 1000 MW coal-fired power plant were in situ treated by high-temperature water vapor. The de-NOx efficiency of the deactivated catalyst increased about 25–30%, comparable to fresh commercial SCR catalysts, after being treated with simulated flue gas with 15–20 vol% high-temperature water vapor. It indicates that treatment by in situ 15–20 vol% high-temperature water vapor could significantly extend the lifetime of commercial SCR catalyst. High-temperature water vapor could remove Fe, Na, Ca, sulphate species and SiO2 depositing on SCR catalyst. Compared with the deactivated catalyst, the specific surface area, the ratio of V4+/V5+ and Lewis acid content of health-care catalyst increased from 41.679 to 44.596 m2·g−1, 1.35 to 1.80 and 45.5 to 73.8%, respectively. Density functional theory (DFT) calculation demonstrated that the electrons transferred from H2O molecule to V5+ cations in the process of H2O adsorption and the subsequent hydroxylation of V5+cations during H2O dissociation contribute to the reduction of V5+ to V4+ on the SCR catalyst.
KW - Commercial SCR catalyst
KW - Health-care
KW - High-temperature water vapor
KW - In situ treatment
UR - http://www.scopus.com/inward/record.url?scp=85097096254&partnerID=8YFLogxK
U2 - 10.1016/j.apsusc.2020.148408
DO - 10.1016/j.apsusc.2020.148408
M3 - 文章
AN - SCOPUS:85097096254
SN - 0169-4332
VL - 541
JO - Applied Surface Science
JF - Applied Surface Science
M1 - 148408
ER -