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On the deactivation of Mo/HZSM-5 in methane dehydroaromatization

By CHL Christiaan Tempelman and EJM Emiel Hensen


The deactivation of Mo/HZSM-5 during the non-oxidative methane aromatization (MDA) reaction that yields benzene and hydrogen was investigated. Catalysts were recovered from the reactor after pre-activation and after increasing time on stream in methane. The physico-chemical properties of the spent catalysts were characterized in detail by Ar physisorption, 27Al MAS NMR and X-ray photoelectron spectroscopy. The nature of the carbon deposits was determined by UV Raman spectroscopy and TGA, and the size and location of the Mo-carbide particles by TEM and STEM-HAADF. The results show that the main cause for catalyst deactivation is the formation of a carbonaceous layer at the external zeolite surface. This layer is made up from polyaromatic hydrocarbons and decreases the accessibility of the Brønsted acid sites in the micropores. At the same time, the decreased interaction of the Mo-carbide particles with the external zeolite surface results in their sintering. The lower Mo-carbide dispersion decreases methane conversion rates. The decreased accessibility of the Brønsted acid sites shifts the selectivity from benzene to unsaturated intermediates formed on the Mo-carbide particles. Silylation of the external surface mainly results in lower rate of coke formation at the external surface, slowing down catalyst deactivatio

Publisher: 'Elsevier BV'
Year: 2015
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Provided by: Repository TU/e
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