Extraordinary Deactivation Offset Effect of Arsenic and Calcium on CeO-WO SCR Catalysts.

Environ Sci Technol

State Key Joint Laboratory of Environment Simulation and Pollution Control, School of Environment , Tsinghua University, Beijing 100084 , P. R. China.

Published: August 2018

AI Article Synopsis

  • A new study revealed that calcium and arsenic together significantly enhance the performance of a CeO-WO catalyst used in reducing nitrogen oxides (NO) with ammonia (NH) at high temperatures.
  • The catalyst achieved up to 89% NO conversion at 350 °C, influencing its structure, surface acidity, and redox properties, as analyzed through various techniques like XRD and XPS.
  • The findings indicated that the interaction between cerium and arsenic improved the catalyst's effectiveness by restoring key acid sites and oxygen defects, with the observed drop in performance linked to reduced surface area and changes in particle structure.

Article Abstract

An extraordinary deactivation offset effect of calcium and arsenic on CeO-WO catalyst had been found for selective catalytic reduction of NO with NH (NH-SCR). It was discovered that the maximum NO conversion of As-Ca poisoned catalyst reached up to 89% at 350 °C with the gaseous hourly space velocity of 120 000 mL·(g·h). The offset effect mechanisms were explored with respect to the changes of catalyst structure, surface acidity, redox property and reaction route by XRD, XPS, H-TPR, O-TPD, NH-TPD and in situ Raman, in situ TG, and DRIFTS. The results manifested that Lewis acid sites and reducibility originating from CeO were obviously recovered, because the strong interaction between cerium and arsenic was weakened when Ca and As coexisted. Meanwhile, the CaWO phase generated on Ca poisoned catalyst almost disappeared after As doping together, which made for Brønsted acid sites reformation on catalyst surface. Furthermore, surface Ce proportion and oxygen defect sites amount were also restored for two-component poisoned catalyst, which favored NH activation and further reaction. Finally, the reasons for the gap of catalytic performance between fresh and As-Ca poisoned catalyst were also proposed as follows: (1) surface area decrease; (2) crystalline WO particles generation; and (3) oxygen defect sites irreversible loss.

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Source
http://dx.doi.org/10.1021/acs.est.8b00746DOI Listing

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