The effect of the Rh–Al, Pt–Al and Pt–Rh–Al surface alloys on NO conversion to N2 on alumina supported Rh, Pt and Pt–Rh catalysts

A. Pietraszek; P. Da Costa; R. Marques; P. Kornelak; Thomas Willum Hansen; J. Camra; M. Najbar

doi:10.1016/j.cattod.2006.08.009

The effect of the Rh–Al, Pt–Al and Pt–Rh–Al surface alloys on NO conversion to N2 on alumina supported Rh, Pt and Pt–Rh catalysts

A. Pietraszek, P. Da Costa, R. Marques, P. Kornelak, Thomas Willum Hansen, J. Camra, M. Najbar

Fritz Haber Institute of the Max Planck Society

Research output: Contribution to journal › Journal article › Research › peer-review

Abstract

NO conversion to N2 in the presence of methane and oxygen over 0.03 at.%Rh/Al2O3, 0.51 at.%Pt/Al2O3 and 0.34 at.%Pt–0.03 at.%Rh/Al2O3 catalysts was investigated. d-Alumina and precious metal–aluminum alloy phases were revealed by XRD and HRTEM in the catalysts. The results of the catalytic activity investigations, with temperature-programmed as well as steady-state methods, showed that NO decomposition occurs at a reasonable rate on the alloy surfaces at temperatures up to 623 K whereas some CH4 deNOx takes place on d-alumina above this temperature. A mechanism for the NO decomposition is proposed herein. It is based on NO adsorption on the precious metal atoms followed by the transfer of electrons from alloy to antibonding p orbitals of NO(ads.) molecules. The CH4 deNOx was shown to occur according to an earlier proposed mechanism, via methane oxidation by NO2(ads.) to oxygenates and then NO reduction by oxygenates to N2.

Original language	English
Journal	Catalysis Today
Volume	119
Pages (from-to)	187-193
DOIs	https://doi.org/10.1016/j.cattod.2006.08.009
Publication status	Published - 2007
Externally published	Yes

Access to Document

10.1016/j.cattod.2006.08.009

OpenUrl availability

Full text

Cite this

@article{2419466f7f0349f693d7d3fed91698df,

title = "The effect of the Rh–Al, Pt–Al and Pt–Rh–Al surface alloys on NO conversion to N2 on alumina supported Rh, Pt and Pt–Rh catalysts",

abstract = "NO conversion to N2 in the presence of methane and oxygen over 0.03 at.%Rh/Al2O3, 0.51 at.%Pt/Al2O3 and 0.34 at.%Pt–0.03 at.%Rh/Al2O3 catalysts was investigated. d-Alumina and precious metal–aluminum alloy phases were revealed by XRD and HRTEM in the catalysts. The results of the catalytic activity investigations, with temperature-programmed as well as steady-state methods, showed that NO decomposition occurs at a reasonable rate on the alloy surfaces at temperatures up to 623 K whereas some CH4 deNOx takes place on d-alumina above this temperature. A mechanism for the NO decomposition is proposed herein. It is based on NO adsorption on the precious metal atoms followed by the transfer of electrons from alloy to antibonding p orbitals of NO(ads.) molecules. The CH4 deNOx was shown to occur according to an earlier proposed mechanism, via methane oxidation by NO2(ads.) to oxygenates and then NO reduction by oxygenates to N2.",

author = "A. Pietraszek and {Da Costa}, P. and R. Marques and P. Kornelak and Hansen, {Thomas Willum} and J. Camra and M. Najbar",

year = "2007",

doi = "10.1016/j.cattod.2006.08.009",

language = "English",

volume = "119",

pages = "187--193",

journal = "Catalysis Today",

issn = "1873-4308",

publisher = "Elsevier",

}

TY - JOUR

T1 - The effect of the Rh–Al, Pt–Al and Pt–Rh–Al surface alloys on NO conversion to N2 on alumina supported Rh, Pt and Pt–Rh catalysts

AU - Pietraszek, A.

AU - Da Costa, P.

AU - Marques, R.

AU - Kornelak, P.

AU - Hansen, Thomas Willum

AU - Camra, J.

AU - Najbar, M.

PY - 2007

Y1 - 2007

N2 - NO conversion to N2 in the presence of methane and oxygen over 0.03 at.%Rh/Al2O3, 0.51 at.%Pt/Al2O3 and 0.34 at.%Pt–0.03 at.%Rh/Al2O3 catalysts was investigated. d-Alumina and precious metal–aluminum alloy phases were revealed by XRD and HRTEM in the catalysts. The results of the catalytic activity investigations, with temperature-programmed as well as steady-state methods, showed that NO decomposition occurs at a reasonable rate on the alloy surfaces at temperatures up to 623 K whereas some CH4 deNOx takes place on d-alumina above this temperature. A mechanism for the NO decomposition is proposed herein. It is based on NO adsorption on the precious metal atoms followed by the transfer of electrons from alloy to antibonding p orbitals of NO(ads.) molecules. The CH4 deNOx was shown to occur according to an earlier proposed mechanism, via methane oxidation by NO2(ads.) to oxygenates and then NO reduction by oxygenates to N2.

AB - NO conversion to N2 in the presence of methane and oxygen over 0.03 at.%Rh/Al2O3, 0.51 at.%Pt/Al2O3 and 0.34 at.%Pt–0.03 at.%Rh/Al2O3 catalysts was investigated. d-Alumina and precious metal–aluminum alloy phases were revealed by XRD and HRTEM in the catalysts. The results of the catalytic activity investigations, with temperature-programmed as well as steady-state methods, showed that NO decomposition occurs at a reasonable rate on the alloy surfaces at temperatures up to 623 K whereas some CH4 deNOx takes place on d-alumina above this temperature. A mechanism for the NO decomposition is proposed herein. It is based on NO adsorption on the precious metal atoms followed by the transfer of electrons from alloy to antibonding p orbitals of NO(ads.) molecules. The CH4 deNOx was shown to occur according to an earlier proposed mechanism, via methane oxidation by NO2(ads.) to oxygenates and then NO reduction by oxygenates to N2.

U2 - 10.1016/j.cattod.2006.08.009

DO - 10.1016/j.cattod.2006.08.009

M3 - Journal article

SN - 1873-4308

VL - 119

SP - 187

EP - 193

JO - Catalysis Today

JF - Catalysis Today

ER -

The effect of the Rh–Al, Pt–Al and Pt–Rh–Al surface alloys on NO conversion to N2 on alumina supported Rh, Pt and Pt–Rh catalysts

Abstract

Access to Document

OpenUrl availability

Fingerprint

Cite this