Affiliation:
1. State Key Laboratory of Molecular & Process Engineering, Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering East China Normal University North Zhongshan Road 3663 Shanghai 200062 China
2. Graduate School of Bio-Applications and Systems Engineering Tokyo University of Agriculture and Technology 2-24-16 Nakacho, Koganei Tokyo 184–8588 Japan
3. Institute of Eco-Chongming Shanghai 202162 China
Abstract
AbstractIn zeolite frameworks, double four‐ring (d4r) configurations are among the most frequent composite building units. The composition variations in d4r units greatly influence the energy and structural modifiability of the zeolitic framework. The introduction of germanium, with a larger ionic radius than silicon or aluminum, not only reduces the energy constraints of d4r in the nucleation and crystal growth of zeolites, but also opens a new window for constructing novel crystalline structures, especially with large or extra‐large pores and channels. Ge‐enriched d4r units endow germanosilicates with structure diversity readily for post treatments. Promising catalytic materials have been gradually developed and increasingly studied by direct synthesis or post‐synthetic isomorphous substitution for Ge. This review focuses on the recent progress in the synthesis, modification, and catalytic application of d4r‐containing zeolites, including germanosilicates, aluminosilicates, and silicates.
Funder
National Natural Science Foundation of China
Subject
General Chemistry,Catalysis,Organic Chemistry
Cited by
3 articles.
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