Formation of Ammonia during the NO−H2 Reaction over Pt/ZrO2
Source abstract
Abstract
The mechanism for the formation of NH 3 during the NO−H 2 reaction over Pt/ZrO 2 was studied. Steady-state isotopic transient kinetic analysis was carried out with isotopic switching from 15 NO−D 2 to 14 NO−D 2, and the results revealed that formation of N 2 and N 2 O was associated with linearly adsorbed NO on the Pt surface, whereas ammonia formation was associated with ND x species adsorbed on ZrO 2 . The adsorbed NH x species were not observed on the surface of ZrO 2 during NH 3 adsorption. From transient kinetic experiments, the formation rates of NH x species and of gaseous NH 3 agreed with each other, suggesting that the NH x species on ZrO 2 was an ammonia intermediate. The ND x species did not react with D 2 directly, but H−D exchange occurred easily. The addition of H 2 O to the NO−H 2 feed gas enhanced the formation of NH 3 . In situ diffuse reflectance spectra and transient kinetic analysis revealed that H 2 O enhanced the conversion of NH x species to NH 3 .
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Catalytic Processes in Materials Science · Ammonia Synthesis and Nitrogen Reduction · Industrial Gas Emission Control
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Research Center for New Fuels and Vehicle Technology, National Institute of Advanced Industrial Science and Technology (AIST), 16-1 Onogawa, Tsukuba 305-8569, Japan, and School of Chemistry, Centre for Theory and Application of Catalysis (CenTACat), Queens University Belfast, Belfast BT9 5AG, U.K.
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