期刊
INORGANIC CHEMISTRY FRONTIERS
卷 9, 期 21, 页码 5444-5453出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2qi01360f
关键词
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资金
- Czech Science Foundation through project EXPRO [19-21534S]
- Czech Science Foundation through OP VVV Excellent Research Teams [CZ.02.1.01/0.0/0.0/15_003/0000417 - CUCAM]
- project Grant Schemes at CU [CZ.02.2.69/0.0/0.0/19_073/0016935]
- Czech Science Foundation [19-21534S]
This study modified the Reverse ADOR process to prepare extra-Large pore zeolite UTL, incorporating a high amount of aluminium into the framework. The modified process significantly reduces synthesis time and improves catalytic performance of the reconstructed UTL zeolite.
Extra-Large pore zeolites dear the way for the synthesis of fine chemicals and bulky compounds unable to enter the channels of medium- and Large-pore zeolites. However, such extra-Large pore zeolites rarely contain catalytically active elements and often show Limited stability. In this study, we modified the Reverse assembly-disassembly-organisation-reassembly (ADOR) process to prepare extra-Large pore zeolite UTL from Layered IPC-1P while simultaneously incorporating a high amount of aluminium (reaching Si/Al = 15) into the framework. Using this modified Reverse ADOR approach, we significantly reduced the synthesis time of alumino-germanosilicate UTL from the 28 days needed for direct synthesis to only 24 hours for reconstruction and 14 days in total. Furthermore, in the tetrahydropyranylation of 1-decanol over the reconstructed UTL zeolite, directly synthesised UTL and commercial Beta zeolite, used as a reference, reconstructed UTL provided conversion up to 61.4%, outperforming directly synthesised UTL and Beta with 14.8 and 0% conversion, respectively. The modified Reverse ADOR procedure enables us to introduce mesoporosity into zeolites, which further improves their catalytic performance by facilitating active site accessibility.
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