Conversion of Methanol to Olefins over H-ZSM-5 Zeolite: Reaction Pathway Is Related to the Framework Aluminum Siting

Abstract

Abstract As the conversion of methanol to olefins (MTO) over a zeolite catalyst is conducted on acid sites derived from framework aluminum (AlF), it is possible to enhance the catalytic performance by altering the siting of AlF if one knows the catalytic behavior of specified AlF located at certain sites. In this work, two series of H-ZSM-5 zeolites, viz., S-HZ-m and T-HZ-m, were synthesized with silica sol and tetraethyl orthosilicate, respectively, as the silicon source. Both series of H-ZSM-5 zeolites exhibit similar acidity, morphology, and textual properties. However, they are quite different with respect to AlF siting, as determined by UV–vis–DRS of Co(II) ions and 27Al MAS NMR; AlF of S-HZ-m is enriched in the sinusoidal and straight channels, whereas AlF of T-HZ-m is concentrated in the channel intersections. When they are used as the catalyst in MTO, T-HZ-m gives higher selectivity to ethene and aromatics and a larger hydrogen transfer index (HTI) than S-HZ-m, whereas S-HZ-m exhibits higher selectivity to propene and higher olefins. Moreover, the 13C/12C-methanol-switching experiments indicate that the incorporation of 12C into pentamethylbenzene and hexamethylbenzene is faster on T-HZ-m, whereas the scramble of 12C for C3–C5 olefins is speedier on S-HZ-m. All of these illustrate that AlF in the channel intersections of H-ZSM-5 is probably more favorable to the propagation of the aromatic-based cycle, whereas AlF in the sinusoidal and straight channels is more encouraging for the alkene-based cycle. These results help to clarify the catalytic behavior of given framework acid sites of H-ZSM-5 in MTO and then bring forward an effective approach to improving the catalytic performance by regulating the framework aluminum siting.