journal article·2008-11-20

Formation of Ammonia during the NO−H2 Reaction over Pt/ZrO2

T. Nanba, F. C. Meunier, C. Hardacre, J. P. Breen, R. Burch, S. Masukawa, J. Uchisawa, A. Obuchi

The Journal of Physical Chemistry C· Volume 112· Issue 46
Publisher page

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 .
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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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