Selective Catalytic Reduction of NO<sub>x</sub> by CO over Doubly Promoted MeMo/Nb<sub>2</sub>O<sub>5</sub> Catalysts (Me = Pt, Ni, or Co)

Doubly promoted MeMo/Nb<sub>2</sub>O<sub>5</sub> catalysts, in which Me = Pt, Ni, or Co oxides were prepared for the selective catalytic reduction of NO<sub>x</sub> by CO reaction (CO-SCR). Comparable chemical, textural, and structural analyses revealed similariti...

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Main Authors: João Pedro S. Nascimento, Lais F. Oton, Alcineia C. Oliveira, Elena Rodríguez-Aguado, Enrique Rodríguez-Castellón, Rinaldo S. Araujo, Monique S. Souza, Rossano Lang
Format: Article
Language:English
Published: MDPI AG 2020-09-01
Series:Catalysts
Subjects:
Online Access:https://www.mdpi.com/2073-4344/10/9/1048
Description
Summary:Doubly promoted MeMo/Nb<sub>2</sub>O<sub>5</sub> catalysts, in which Me = Pt, Ni, or Co oxides were prepared for the selective catalytic reduction of NO<sub>x</sub> by CO reaction (CO-SCR). Comparable chemical, textural, and structural analyses revealed similarities between NiMo and CoMo impregnated on Nb<sub>2</sub>O<sub>5</sub>, in contrast to PtMo sites, which were not homogeneously dispersed on the support surface. Both the acid function and metal dispersion gave a synergistic effect for CO-SCR at moderate temperatures. The reactivity of PtMo catalysts towards NO<sub>x</sub> and CO chemisorption was at low reaction temperatures, whereas the NO<sub>x</sub> conversion over CoMo was greatly improved at relatively high temperatures. Careful XPS, NH<sub>3</sub>-TPD, and HRTEM analyses confirmed that the large amounts of strong and moderate acid sites from PtO<sub>x</sub> entrapped on MoO<sub>3</sub> sites induced high NO<sub>x</sub> conversions. NiMo/Nb<sub>2</sub>O<sub>5</sub> showed poor performance in all conditions. Poisoning of the MeMo sites with water vapor or SO<sub>2</sub> (or both) provoked the decline of the NO<sub>x</sub> conversions over NiMo and PtMo sites, whereas the structure of CoMo ones remained very active with a maximum NO<sub>x</sub> conversion of 70% at 350 °C for 24 h of reaction. This was due to the interaction of the Co<sup>3+</sup>/Co<sup>2+</sup> and Mo<sup>6+</sup> actives sites and the weak strength Lewis acid Nb<sup>5+</sup> ones, as well.
ISSN:2073-4344