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Catalyst Deactivation Modes of PdO/γ-Al2O3 Catalysts for Lean Methane Oxidation
Catalyst Deactivation Modes of PdO/γ-Al2O3 Catalysts for Lean Methane Oxidation
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Catalyst Deactivation Modes of PdO/γ-Al2O3 Catalysts for Lean Methane Oxidation
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Catalyst Deactivation Modes of PdO/γ-Al2O3 Catalysts for Lean Methane Oxidation
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Catalyst Deactivation Modes of PdO/γ-Al2O3 Catalysts for Lean Methane Oxidation
Catalyst Deactivation Modes of PdO/γ-Al2O3 Catalysts for Lean Methane Oxidation
Journal Article

Catalyst Deactivation Modes of PdO/γ-Al2O3 Catalysts for Lean Methane Oxidation

2025
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Overview
PdO/γ-Al2O3 catalysts are one of the most active catalytic components for the complete oxidation of methane. Under reaction conditions, especially in a wet feed, the catalysts suffer severe performance degradation. This study establishes a series of testing protocols to systematically investigate the causes of catalyst deactivation under methane oxidation reaction conditions. Four distinct catalyst deactivation modes are identified. Two of the deactivation modes are directly related to H2O, either from the feed gas or as a part of the reaction products, with one (Mode 2) being attributed to the formation of surface hydroxyl groups and the other (Mode 3) to the competitive adsorption of H2O on the catalysts. The impact of the two deactivation modes is acute and severe but reversible. In contrast, the other two deactivation modes are gradual and persistent but irreversible. Both modes are induced by CH4 oxidation reaction, with the impact of a wet feed (Mode 4) being substantially more severe than that of a dry feed (Mode 1). The major cause of the irreversible catalyst deactivation is attributed to surface reconstruction of PdO nanoparticles, which behaves as a passivation layer lowering the number of coordinately unsaturated Pd sites for CH4 activation. Although the passivation layer is relatively stable against thermal or hydrothermal treatment, it is not completely inert. Formation and partial regeneration of the passivation layer is a highly dynamic process and heavily depends on the reaction temperature: a lower reaction temperature (≤ 450 ℃) can lead to quicker catalyst deactivation; but a higher reaction temperature (between 500 – 550 ℃) can result in a greater extent of catalyst deactivation.

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