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The effect of Cl- on CeO2-WO3/TiO2 catalyst for selective catalytic reduction of NO with NH3
被引:2
作者:

Yang, Yuming
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Northeastern Univ, Sch Met, 3-11 Wenhua Rd, Shenyang 110819, Peoples R China Northeastern Univ, Sch Met, 3-11 Wenhua Rd, Shenyang 110819, Peoples R China

Bian, Xue
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Northeastern Univ, Sch Met, 3-11 Wenhua Rd, Shenyang 110819, Peoples R China Northeastern Univ, Sch Met, 3-11 Wenhua Rd, Shenyang 110819, Peoples R China

Xie, Feng
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Northeastern Univ, Sch Met, 3-11 Wenhua Rd, Shenyang 110819, Peoples R China Northeastern Univ, Sch Met, 3-11 Wenhua Rd, Shenyang 110819, Peoples R China

Bai, Yuting
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机构:
Liaoning Inst Sci & Technol, Sch Met & Mat Engn, Benxi 117004, Peoples R China Northeastern Univ, Sch Met, 3-11 Wenhua Rd, Shenyang 110819, Peoples R China
机构:
[1] Northeastern Univ, Sch Met, 3-11 Wenhua Rd, Shenyang 110819, Peoples R China
[2] Liaoning Inst Sci & Technol, Sch Met & Mat Engn, Benxi 117004, Peoples R China
关键词:
Denitration;
CeO2-WO3/TiO2;
C1(-)poisoning mechanism;
NH3-SCR;
LOW-TEMPERATURE NH3-SCR;
MIXED-OXIDE;
MNOX/TIO2;
CATALYST;
NITROGEN-OXIDES;
SO2;
PERFORMANCE;
SCR;
CE;
DEACTIVATION;
MECHANISM;
D O I:
10.1016/j.apsusc.2024.162131
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
The 30CeO(2)-4WO(3)/TiO2 catalyst was prepared utilizing cost-effective cerium chloride instead of the traditional cerium nitrate as the cerium source in this paper. The structure, physical and chemical properties, catalytic performance were characterized. The catalytic performance and N-2 selectivity of the 30CeO(2)-4WO(3)/TiO2 catalyst significantly deteriorate with increased the content of Cl-. Specifically, denitration efficiency of 30CeO(2)-4WO(3)/TiO2-0.007 % exceeding 80 % and 90 % were 225 similar to 520 degrees C and 241 similar to 504 degrees C, respectively, whereas the maximum denitration efficiency of the 30CeO(2)-4WO(3)/TiO2-0.161 % sample was only 79.83 %. The effect mechanism of Cl- on catalytic performance was discussed. (1) XRD and BET results show that Cl- can cause the expansion of the lattice of TiO2 and CeO2, thereby increasing its crystallinity and decreasing the specific surface area. (2) Cl- interacts with NH4+ to form NH4Cl, which subsequently reacts with CeO2 to produce CeOCl, leading to the obstruction of the catalyst's micropores. (3) XPS, NH3-TPD, and H-2-TPR analyses reveal that Cl- would occupy the oxygen vacancies, impeding oxygen migration and diminishing active surface centers. (4) In-situ DRIFTs analysis demonstrates that elevated Cl- concentrations diminish NH3 adsorption capacity and facilitate nitrate species formation. The accumulation of nitrates was a primary cause of the decline in catalyst activity.
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