Abstract
Currently, synthesizing zeolites with specific physicochemical properties in a more environmentally benign and safe way is challenging. Herein we report a novel ionothermal route of preparing HZSM-5 zeolite, which is featured by the direct interzeolite transformation of HY to HZSM-5. The appropriate synthetic conditions of this HZSM-5 material are refined. Although performing a series of optimization, the resultant product still contains minor (NH4)3AlF6 impurity. Pure HZSM-5 phase with high relative crystallinity can be obtained through successive calcination and acid-washing treatments towards the as-made sample. SEM–EDS characterization and nitrogen physisorption measurement reveal that this pure HZSM-5 sample is composed of classical coffin-like crystals with a low Si/Al ratio and evident hierarchical micro-mesoporous structure. Benefiting from its unique physicochemical properties, this pure HZSM-5 catalyst exhibits more superior methanol-to-aromatics performance than those of the state-of-the-art HZSM-5 and Metal/ZSM-5 catalysts evaluated under similar reaction conditions. It can be anticipated that this HZSM-5 material may be applied in other industrially relevant reactions owing to its particular structure and properties.
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Acknowledgements
This work was supported by the National Natural Science Foundation of China (Grant No. 21666019, 22168022) and The Youth Natural Science Foundation of Gansu Province (Grant No. 20JR10RA189). We cordially thank the Reviewers and Editors for providing us with valuable comments and suggestions.
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Mr. ZY wrote the original draft. Ms. YL conducted the material syntheses. Dr. DW analyzed the XRD data. Dr. XL conducted the SEM analysis. Dr. HL measured the catalytic performance. Prof. XZ proposed the project and revised the draft.
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Yang, Z., Li, Y., Wang, D. et al. Interzeolite conversion of HY to hierarchical HZSM-5 catalyst via an ionothermal route and its excellent catalytic performance in methanol-to-aromatics reaction. J Porous Mater 29, 1039–1047 (2022). https://doi.org/10.1007/s10934-022-01227-z
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DOI: https://doi.org/10.1007/s10934-022-01227-z