том 13 издание 10 страницы 4607

In situ Raman and in situ XRD analysis of PdO reduction and Pd° oxidation supported on γ-Al2O3 catalyst under different atmospheres

Тип публикацииJournal Article
Дата публикации2011-01-31
scimago Q2
wos Q2
БС2
SJR0.698
CiteScore5.3
Impact factor2.9
ISSN14639076, 14639084
Physical and Theoretical Chemistry
General Physics and Astronomy
Краткое описание
Reduction of Pd° and decomposition of palladium oxide supported on γ-alumina were studied at atmospheric pressure under different atmospheres (H(2), CH(4), He) over a 4 wt% Pd/Al(2)O(3) catalyst (mean palladium particle size: 5 nm with 50% of small particles of size below 5 nm). During temperature programmed tests (reduction, decomposition and oxidation) the crystal domain behaviour of the PdO/Pd° phase was evaluated by in situ Raman spectroscopy and in situ XRD analysis. Under H(2)/N(2), the reduction of small PdO particles (<5 nm) occurs at room temperature, whereas reduction of larger particles (>5 nm) starts at 100 °C and is achieved at 150 °C. Subsequent oxidation in O(2)/N(2) leads to reoxidation of small crystal domain at ambient temperature while oxidation of large particles starts at 300 °C. Under CH(4)/N(2), the small particle reduction occurs between 240 and 250 °C while large particle reduction is fast and occurs between 280 and 290 °C. Subsequent reoxidation of the catalyst reduced in CH(4)/N(2) shows that small and large particle oxidation of Pd° starts also at 300 °C. Under He, no small particle decomposition is observed probably due to strong interactions between particles and support whereas large particle reduction occurs between 700 and 750 °C. After thermal decomposition under He, the oxidation starts at 300 °C. Thus, the reduction phenomenon (small and large crystal domain) depends on the nature of the reducing agent (H(2), CH(4), He). However, whatever the reduction or decomposition treatment or the crystal domain, Pd° oxidation starts at 300 °C and is completed only at temperatures higher than 550 °C. Under lean conditions, with or without water, the palladium consists of reduced sites of palladium (Pd°, Pd(δ+) with δ < 2 or PdO(x) with x < 1) randomly distributed on palladium particles.
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Baylet A. et al. In situ Raman and in situ XRD analysis of PdO reduction and Pd° oxidation supported on γ-Al2O3 catalyst under different atmospheres // Physical Chemistry Chemical Physics. 2011. Vol. 13. No. 10. p. 4607.
ГОСТ со всеми авторами (до 50) Скопировать
Baylet A., Marécot P., Duprez D., Castellazzi P., Groppi G., Forzatti P. In situ Raman and in situ XRD analysis of PdO reduction and Pd° oxidation supported on γ-Al2O3 catalyst under different atmospheres // Physical Chemistry Chemical Physics. 2011. Vol. 13. No. 10. p. 4607.
RIS |
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TY - JOUR
DO - 10.1039/c0cp01331e
UR - https://doi.org/10.1039/c0cp01331e
TI - In situ Raman and in situ XRD analysis of PdO reduction and Pd° oxidation supported on γ-Al2O3 catalyst under different atmospheres
T2 - Physical Chemistry Chemical Physics
AU - Baylet, Alexandre
AU - Marécot, Patrice
AU - Duprez, Daniel
AU - Castellazzi, Paola
AU - Groppi, Gianpiero
AU - Forzatti, P.
PY - 2011
DA - 2011/01/31
PB - Royal Society of Chemistry (RSC)
SP - 4607
IS - 10
VL - 13
PMID - 21279224
SN - 1463-9076
SN - 1463-9084
ER -
BibTex |
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@article{2011_Baylet,
author = {Alexandre Baylet and Patrice Marécot and Daniel Duprez and Paola Castellazzi and Gianpiero Groppi and P. Forzatti},
title = {In situ Raman and in situ XRD analysis of PdO reduction and Pd° oxidation supported on γ-Al2O3 catalyst under different atmospheres},
journal = {Physical Chemistry Chemical Physics},
year = {2011},
volume = {13},
publisher = {Royal Society of Chemistry (RSC)},
month = {jan},
url = {https://doi.org/10.1039/c0cp01331e},
number = {10},
pages = {4607},
doi = {10.1039/c0cp01331e}
}
MLA
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Baylet, Alexandre, et al. “In situ Raman and in situ XRD analysis of PdO reduction and Pd° oxidation supported on γ-Al2O3 catalyst under different atmospheres.” Physical Chemistry Chemical Physics, vol. 13, no. 10, Jan. 2011, p. 4607. https://doi.org/10.1039/c0cp01331e.