Source abstract
Abstract
ABSTRACT The spatial distribution of aluminum in zeolites plays a crucial role in optimizing their catalytic performance. Existing strategies often rely on combinations of inorganic and organic structure‐directing agents to guide crystal growth and aluminum incorporation. However, these methods typically result in zeolite crystals with an aluminum‐rich surface, providing limited control over the spatial placement of aluminum within the crystal structure. In this study, we explore an alternative “weaving” strategy aimed at synthesizing zeolites with alternating Al‐rich and Si‐rich nanodomains within single crystals. This approach involves the physical blending of two separately aged, amorphous sols with contrasting Si/Al ratios, followed by freeze‐drying and steam‐assisted crystallization of the resulting solid in vapor. Unlike conventional hydrothermal synthesis, which produces zeolites with Al‐enriched crystal surfaces, this modularized assembly enables systematic modulation of aluminum distribution, resulting in zeolite crystals with comparable bulk and surface Si/Al ratios, an uncommon feature for high‐silica zeolites. The resulting interwoven zeolites, with closely matched bulk and surface Si/Al ratios, exhibit nearly a twofold increase in catalytic lifetime in the methanol‐to‐hydrocarbons reaction compared to a reference zeolite with a similar bulk composition but significant surface aluminum enrichment, underscoring the significant impact of aluminum spatial distribution on catalytic stability.
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Affiliations
State Key Laboratory of Heavy Oil Processing College of Chemistry and Chemical Engineering China University of Petroleum (East China) Qingdao China
Laboratoire de Catalyse et Spectrochimie, LCS UMR 6506 ENSICAEN France
Univ Rouen Normandie, INSA Rouen Normandie, CNRS Groupe de Physique des Matériaux UMR 6634 Rouen France
Advanced Material Analysis Co‐creation Research Center, Institute of Multidisciplinary Research for Advanced Materials Tohoku University Sendai Japan
Application planning group, JEOL Ltd. Tokyo Japan
Beijing Key Laboratory of Green Chemical Reaction Engineering and Technology, Department of Chemical Engineering Tsinghua University Beijing China
Petrochemical Research Institute PetroChina Company Limited Beijing China
Funding
National Natural Science Foundation of China