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Titolo:
Structure and properties of cobalt-exchanged H-ZSM5 catalysts for dehydrogenation and dehydrocyclization of alkanes
Autore:
Li, W; Yu, SY; Meitzner, GD; Iglesia, E;
Indirizzi:
Univ Calif Berkeley, Dept Chem Engn, Berkeley, CA 94720 USA Univ Calif Berkeley Berkeley CA USA 94720 em Engn, Berkeley, CA 94720 USA Edge Analyt, Middleton, WI 53562 USA Edge Analyt Middleton WI USA 53562Edge Analyt, Middleton, WI 53562 USA
Titolo Testata:
JOURNAL OF PHYSICAL CHEMISTRY B
fascicolo: 6, volume: 105, anno: 2001,
pagine: 1176 - 1184
SICI:
1520-6106(20010215)105:6<1176:SAPOCH>2.0.ZU;2-6
Fonte:
ISI
Lingua:
ENG
Soggetto:
PROPANE; ZEOLITES; HYDROCARBONS; CALCINATION; REDUCTION; CATIONS; DENSITY; METHANE; ZSM-5; EDGE;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Physical, Chemical & Earth Sciences
Citazioni:
31
Recensione:
Indirizzi per estratti:
Indirizzo: Iglesia, E Univ Calif Berkeley, Dept Chem Engn, Berkeley, CA 94720 USA Univ Calif Berkeley Berkeley CA USA 94720 rkeley, CA 94720 USA
Citazione:
W. Li et al., "Structure and properties of cobalt-exchanged H-ZSM5 catalysts for dehydrogenation and dehydrocyclization of alkanes", J PHYS CH B, 105(6), 2001, pp. 1176-1184

Abstract

Co/H-ZSM5 catalysts with Co/Al ratios of 0.09-0.22 were prepared by aqueous exchange. Turnover rates for propane conversion to propene and to C-6-C-8aromatics on these catalysts are about 10-fold higher than on H-ZSM5. The selectivities to propene, aromatics, and H-2 are also higher on Co/H-ZSM5 than on H-ZSM5. The rate of D-2 exchange with OH groups increases with increasing Co/Al ratio, suggesting that Co cations catalyze D-2 dissociative chemisorption steps that limit the rate of isotopic exchange. Co cations also catalyze hydrogen recombinative desorption steps, which limit the rate of propane dehydrogenation and aromatization reactions. The density of residualzeolitic hydroxyls was measured by D-2-OB isotopic exchange and by changesin the intensity of OH infrared bands as a function of Co content. D-2-OH and infrared measurements showed that Co2+ cations replace 1.1-1.3 zeoliticprotons, suggesting the predominant presence of Co2+- O-Co2+ dimers, with some Co2+ monomers, each bridging two next-nearest neighbor Al sites. The location and structure of exchanged Co cations were probed using X-ray absorption spectroscopy (XAS) and temperature-programmed reduction (TPR). No Hz consumption was detected up to 1273 K during TPR in any of the Co/H-ZSM5 samples, consistent with the absence of CoOx crystallites, which reduce at similar to 800 K. In situ near-edge X-ray absorption studies confirmed that Co species remain as divalent cations during exposure to H-2 or C3H8 at 773 K. Near-edge and fine structure analysis detected Co2+ cations with similarstructure in all Co/H-ZSM5 samples (Co/Al < 0.22), and Co coordination changes from octahedral to tetrahedral upon sample dehydration at 773 K in He. Radial structure functions showed weak contributions from the first and second shells around Co. This reflects the nonunifomm nature of the distance and orientation in Al-Al next-nearest neighbor sites in ZSM5.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 09/07/20 alle ore 00:29:07