http://www.cnr.it/ontology/cnr/individuo/prodotto/ID42586
On the role of redox properties of CuO/CeO2 catalysts in the preferential oxidation of CO in H2-rich gases (Articolo in rivista)
- Type
- Label
- On the role of redox properties of CuO/CeO2 catalysts in the preferential oxidation of CO in H2-rich gases (Articolo in rivista) (literal)
- Anno
- 2008-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.apcata.2008.06.025 (literal)
- Alternative label
T. Caputo, L. Lisi, R. Pirone, G. Russo (2008)
On the role of redox properties of CuO/CeO2 catalysts in the preferential oxidation of CO in H2-rich gases
in Applied catalysis. A, General (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- T. Caputo, L. Lisi, R. Pirone, G. Russo (literal)
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- Rivista
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- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Dipartimento di Ingegneria Chimica, Universita` degli Studi ''Federico II'' di Napoli, P.le Tecchio, 80 Napoli, Zip code: I-80125, Italy
Istituto di Ricerche sulla Combustione (CNR), P.le Tecchio, 80 Napoli, Zip code: I-80125, Italy (literal)
- Titolo
- On the role of redox properties of CuO/CeO2 catalysts in the preferential oxidation of CO in H2-rich gases (literal)
- Abstract
- CuO/CeO2 catalysts with CuO content ranging from 0.5 wt.% to 8 wt.%, prepared by wet impregnation of
commercial ceria, have been tested for the preferential oxidation of CO (CO-PROX) under H2-rich
conditions at 70-210 8C. Catalytic activity increases up to 4 wt.% CuO content, with less concentrated
catalysts showing higher intrinsic activity. Catalysts have been characterized by means of XRD, BET
analysis and UV spectroscopy. Formation of segregated CuO clusters has been detected for Cu richest
CuO/CeO2 sample. Redox properties have been deeply investigated using TP analysis (H2 TPR, CO TPR,
TPO) of fresh or pre-treated samples. Participation of surface ceria, induced by the strong interaction with
copper, to reduction/oxidation reactions in the temperature range explored (up to 430 8C) has been
demonstrated. Different copper species and their reactivity towards H2 and CO have been individuated by
comparing TPR of fully oxidized catalysts with those of partially oxidized catalysts. Active species have
been identified as copper-ceria sites able to oxidize CO even at room temperature and to be re-oxidized
by O2 at the same temperature. Transient experiments have been carried out at different temperature
using a diluted mixture starting from oxidized or reduced catalysts and followed by a H2 TPR of the used
samples. The results of these tests have showed that active centres for CO oxidation contain copper in the
+2 oxidation state. At T > 100 8C some reduced copper sites are stabilized which promote H2 oxidation
thus lowering the selectivity of the CO-PROX process. (literal)
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