Issue 20, 2021, Issue in Progress

Yttrium stabilization and Pt addition to Pd/ZrO2 catalyst for the oxidation of methane in the presence of ethylene and water

Abstract

Catalytic oxidation is the most efficient method of minimizing the emissions of harmful pollutants and greenhouse gases. In this study, ZrO2-supported Pd catalysts are investigated for the catalytic oxidation of methane and ethylene. Pd/Y2O3-stabilized ZrO2 (Pd/YSZ) catalysts show attractive catalytic activity for methane and ethylene oxidation. The ZrO2 support containing up to 8 mol% Y2O3 improves the water resistance and hydrothermal stability of the catalyst. All catalysts are characterized by X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET), O2-temperature-programmed desorption (O2-TPD), and CO-chemisorption techniques. It shows that high Pd dispersion and Pd–PdO reciprocation on the Pd/YSZ catalyst results in relatively high stability. In situ diffuse reflectance infrared Fourier-transform (DRIFT) experiments are performed to study the reaction over the surface of the catalyst. Compared with bimetallic catalysts (Pd : Pt), the same amounts of Pd and Pt supported on ZrO2 and Y2O3-stabilized ZrO2 catalysts show enhanced activity for methane and ethylene oxidation, respectively. A mixed hydrocarbon feed, containing methane and ethylene, lowers the CH4 light-off temperature by approximately 80 °C. This shows that ethylene addition has a promotional effect on the light-off temperature of methane.

Graphical abstract: Yttrium stabilization and Pt addition to Pd/ZrO2 catalyst for the oxidation of methane in the presence of ethylene and water

Supplementary files

Article information

Article type
Paper
Submitted
23 Dec 2020
Accepted
06 Mar 2021
First published
23 Mar 2021
This article is Open Access
Creative Commons BY license

RSC Adv., 2021,11, 11910-11917

Yttrium stabilization and Pt addition to Pd/ZrO2 catalyst for the oxidation of methane in the presence of ethylene and water

H. A. Khan, J. Hao, O. E. Tall and A. Farooq, RSC Adv., 2021, 11, 11910 DOI: 10.1039/D0RA10773E

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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