Gas-Phase Regeneration of Metal-Poisoned V2O5-WO3/TiO2 NH3-SCR Catalysts via a Masking and Reconstruction Strategy

被引:8
|
作者
Wang, Sha [1 ]
Liu, Jun [1 ]
Jin, Zaisheng [1 ]
Guo, Shiqi [1 ]
Cheng, Danhong [1 ]
Deng, Jiang [1 ]
Zhang, Dengsong [1 ]
机构
[1] Shanghai Univ, Coll Sci, Res Ctr Nano Sci & Technol, Dept Chem,Innovat Inst Carbon Neutral,Int Joint La, Shanghai 200444, Peoples R China
基金
中国国家自然科学基金;
关键词
selective catalytic reduction; NO x elimination; heavy metalpoisoning; gas-basedregeneration; active sites reconstruction; COMMERCIAL SCR CATALYSTS; LOW-TEMPERATURE NH3-SCR; REACTION-MECHANISM; ACTIVE-SITES; NITRIC-OXIDE; ACID SITES; VANADIUM; SO2; NOX; REDUCTION;
D O I
10.1021/acs.est.4c05260
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Renewing metal-poisoned NH3-SCR catalysts holds great potential for mitigating environmental pollution and utilizing hazardous wastes simultaneously. Ionic compounds containing heavy metals often exhibit limited solubility due to their high polarizability, making traditional washing techniques ineffective in removing heavy metal poisons. This study presents a gas-based method for regenerating heavy-metal-poisoned V2O5-WO3/TiO2 catalysts employed in NH3-SCR techniques. The regeneration is achieved by employing a masking and reconstruction strategy, which involves the in situ formation of NO2 to mediate the production of SO3. This enables the effective bonding of Pb and triggers the reconstruction of active VOx sites. In situ spectroscopy confirms that the sulfation of PbO restores acidity, while the occupied effect resulting from the sulfation of TiO2 promotes the formation of more polymeric VOx species. Consequently, the regenerated catalyst exhibits enhanced activity and superior resistance to metal poisons compared with the fresh catalyst. The innovative method offers a promising solution for extending the lifespan of poisoned catalysts, reducing waste generation, and enhancing the efficiency of NH3-SCR systems.
引用
收藏
页码:13574 / 13584
页数:11
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