Journal
CATALYSIS SCIENCE & TECHNOLOGY
Volume 7, Issue 3, Pages 607-618Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c6cy02564a
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Funding
- National Natural Science Foundation of China [21303089, 21303087, 21421001]
- Municipal Natural Science Foundation of Tianjin [13JCQNJC05900, 13RCGFGX01124, 14JCQNJC05700]
- Ministry of Education of China [IRT-13022]
- Deutsche Forschungsgemeinschaft [HU533/13-1]
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Low-silica AlPO-34 materials with similar crystal sizes but different Bronsted acid site densities were prepared and investigated as catalysts in methanol-to-olefin (MTO) conversion. The effect of Bronsted acid site density on catalyst activity and the dominant reaction mechanism during the MTO conversion was investigated via TGA, GC-MS, solid-state NMR spectroscopy, and in situ UV/vis spectroscopy together with the catalytic performance. For the catalysts with lower Bronsted acid site densities, the olefin-based cycle mechanism is the dominant mechanism during the MTO conversion. Long-chain alkenes, e.g., C-5=-C-6=alkenes, act as intermediates that are cracked to lower olefins, or are converted to dienes via hydride transfer reactions, and can also diffuse out of the cages of low-silica AlPO-34 catalysts as the products. With decreasing Bronsted acid site density or reaction temperature, the methylation route of the olefin-based cycle was found to be much more favored than the cracking route. Therefore, a higher selectivity to C-5=C-6=alkenes (similar to 50%) is achieved. Simultaneously, dienes are the predominant deposits occluded in the used catalysts. For catalysts with slightly higher Bronsted acid site densities, the long-chain alkenes are rapidly transformed to aromatics and, subsequently, an aromatic-based cycle mechanism contributes to the MTO conversion. Interestingly, the catalyst with the most suitable Bronsted acid site density can well balance the above-mentioned two reaction cycles accompanied by a low deactivation rate, leading to a long catalyst lifetime of up to 15 h.
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