http://www.cnr.it/ontology/cnr/individuo/prodotto/ID304294
Methane oxidation on Pd@ZrO2/Si-Al2O3 is enhanced by surface reduction of ZrO2 (Articolo in rivista)
- Type
- Label
- Methane oxidation on Pd@ZrO2/Si-Al2O3 is enhanced by surface reduction of ZrO2 (Articolo in rivista) (literal)
- Anno
- 2014-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1021/cs501146u (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Chen C.; Yeh Y.-H.; Cargnello M.; Murray C.B.; Fornasiero P.; Gorte R.J. (literal)
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- http://www.scopus.com/inward/record.url?eid=2-s2.0-84909954555&partnerID=q2rCbXpz (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
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- Department of Chemical and Biomolecular Engineering, University of Pennsylvania, 231 South 34th Street, Philadelphia, PA, 19104, United States; Department of Chemistry, University of Pennsylvania, 231 South 34th Street, Philadelphia, PA, 19104, United States; Department of Materials Science and Engineering, University of Pennsylvania, 3131 Walnut Street, Philadelphia, PA, 19104, United States; Department of Chemical and Pharmaceutical Sciences, ICCOM-CNR, University of Trieste, via L. Giorgieri 1, Trieste, 34127, Italy (literal)
- Titolo
- Methane oxidation on Pd@ZrO2/Si-Al2O3 is enhanced by surface reduction of ZrO2 (literal)
- Abstract
- The catalytic properties of Pd@ZrO2 core-shell catalysts supported on Si-modified alumina were studied for application to methane oxidation and compared to the analogous Pd@CeO2 catalysts. In the absence of water (dry conditions), both Pd@ZrO2 and Pd@CeO2 were highly active and showed nearly identical reaction rates and thermal stabilities. However, unlike catalysts based on Pd@CeO2, the Pd@ZrO2 catalysts were also very stable in the presence of high concentrations of water vapor. By means of Coulometric titration and pulse-reactor studies, we demonstrate that ZrO2 in contact with Pd can be reduced. Additionally, Coulometric titration showed that the Pd-PdO equilibrium at 600 °C is shifted to much lower P(O2) in the Pd@ZrO2 catalyst compared to conventional Pd/ZrO2 or Pd/Al2O3 catalysts. Because PdO is more active for methane oxidation, this observation provides a possible explanation for the superior performance of the Pd@ZrO2 catalyst. (literal)
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