Continuous De-NO<sub><i>x</i></sub> underRich/Lean Cycles by Multifunctional Catalysis of Platinum-Loaded Mordenites

Limited catalytic methods have been reported for urea-free lean NO<sub><i>x</i></sub> emission control. This study reports a continuous and cyclic de-NO<sub><i>x</i></sub> system utilizing mordenite-supported low-loading (0.3 wt %) platinum, Pt(0.3)/MOR, as a multifunctional catalytic and NH<sub>3</sub> storage material. Under alternating feeds of rich (0.1% NO + 0.5% CO + 1% H<sub>2</sub>O) and lean (0.1% NO + 2% O<sub>2</sub> + 1% H<sub>2</sub>O) gas mixtures, Pt(0.3)/MOR demonstrated higher de-NO<sub><i>x</i></sub> efficiency under relatively lean conditions compared to the steady-state reaction in a temperature range of 300–500 °C. The de-NO<sub><i>x</i></sub> mechanism under periodic rich/lean conditions on Pt(0.3)/MOR was investigated using operando infrared experiments. During the rich period, the Pt-catalyzed water–gas shift reaction gives H<sub>2</sub> which reduces NO into in situ formed NH<sub>3</sub>. The generated NH<sub>3</sub> is subsequently captured by the Brønsted acid sites of the zeolite support. In the subsequent lean period, NO is reduced by adsorbed NH<sub>3</sub> on Pt sites. This study presents a new multifunctional material for a urea-free de-NO<sub><i>x</i></sub> system, offering a potential alternative for automotive de-NO<sub><i>x</i></sub> applications.

Publication Details

Journal
Figshare
Published
2025-03-11
DOI
https://doi.org/10.1021/acsestengg.5c00113.s001
Primary Topic
Catalytic Processes in Materials Science
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article
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article

Continuous De-NOx underRich/Lean Cycles by Multifunctional Catalysis of Platinum-Loaded Mordenites

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Catalytic Processes in Materials Science
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Continuous De-NOx underRich/Lean Cycles by Multifunctional Catalysis of Platinum-Loaded Mordenites

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Abstract

Limited catalytic methods have been reported for urea-free lean NO<sub><i>x</i></sub> emission control. This study reports a continuous and cyclic de-NO<sub><i>x</i></sub> system utilizing mordenite-supported low-loading (0.3 wt %) platinum, Pt(0.3)/MOR, as a multifunctional catalytic and NH<sub>3</sub> storage material. Under alternating feeds of rich (0.1% NO + 0.5% CO + 1% H<sub>2</sub>O) and lean (0.1% NO + 2% O<sub>2</sub> + 1% H<sub>2</sub>O) gas mixtures, Pt(0.3)/MOR demonstrated higher de-NO<sub><i>x</i></sub> efficiency under relatively lean conditions compared to the steady-state reaction in a temperature range of 300–500 °C. The de-NO<sub><i>x</i></sub> mechanism under periodic rich/lean conditions on Pt(0.3)/MOR was investigated using operando infrared experiments. During the rich period, the Pt-catalyzed water–gas shift reaction gives H<sub>2</sub> which reduces NO into in situ formed NH<sub>3</sub>. The generated NH<sub>3</sub> is subsequently captured by the Brønsted acid sites of the zeolite support. In the subsequent lean period, NO is reduced by adsorbed NH<sub>3</sub> on Pt sites. This study presents a new multifunctional material for a urea-free de-NO<sub><i>x</i></sub> system, offering a potential alternative for automotive de-NO<sub><i>x</i></sub> applications.

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Catalytic Processes in Materials Science
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