IR Study on the Mechanism of Room Temperature Methane and Benzene Interaction with alfa-Oxygen over Fe-ZSM-5 zeolites Conference Abstracts
Conference |
220th ACS National Meeting: Symposium "Metal Oxide Catalysts: Active Sites, Intermediates and Reaction Mechanisms" 20-24 Aug 2000 , Washington, DC |
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Abstracts of Papers of the American Chemical Society
ISSN: 0065-7727 |
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Output data | Year: 2000, Volume: 220, Number: part 1, Article number : COLL-282, Pages count : 1 | ||
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Abstract:
Earlier, iron complexes in ZSM-5 matrix have been shown to generate from nitrous oxide active oxygen species
(alfa-oxygen) responsible for the zeolite activity in selective oxidation of hydrocarbons. In the present work,
IR-spectroscopy, adsorption and isotope methods have been used to investigate the mechanism of alfa-oxygen interaction with methane, benzene and hydrogen at room temperature on the FeZSM-5 surface. Methane interaction is accompanied by its dissociation yielding methoxy (2823, 2920, 2945 and 2964 cm-1) and hydroxy (3635 and 3673 cm-1) groups bonded to alfa-oxygen. The high value of the kinetic isotope effect (kH/kD=3.2) indicates that the C-H bond cleavage is the rate limiting step. Hydrogen interaction also results in the dissociation producing two OH groups per each mol. Contrary to that, benzene interacts with alfa-oxygen most likely via the formation of an epoxy-type intermediate without the C-H bond breaking at a rate limiting step.
Cite:
Dubkov K.A.
, Paukshtis E.A.
, Panov G.I.
IR Study on the Mechanism of Room Temperature Methane and Benzene Interaction with alfa-Oxygen over Fe-ZSM-5 zeolites
Abstracts of Papers of the American Chemical Society. 2000. V.220. Npart 1. COLL-282 :1-1. WOS РИНЦ AN
IR Study on the Mechanism of Room Temperature Methane and Benzene Interaction with alfa-Oxygen over Fe-ZSM-5 zeolites
Abstracts of Papers of the American Chemical Society. 2000. V.220. Npart 1. COLL-282 :1-1. WOS РИНЦ AN
Dates:
Published print: | Aug 1, 2000 |
Identifiers:
Web of science: | WOS:000166091201416 |
Elibrary: | 46663712 |
Chemical Abstracts: | 2000:794474 |
Citing:
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