Controlling the competitive growth of zeolite phases without using an organic structure-directing agent. Synthesis of Al-rich *BEA

沸石 结晶 水热合成 化学工程 材料科学 溶解 热液循环 相(物质) 产量(工程) 亚稳态 溶解度 化学 有机化学 催化作用 复合材料 工程类
作者
Radim Pilař,Jaroslava Morávková,Galina Sádovská,Štěpán Sklenák,Libor Brabec,Jana Pastvová,Petr Sazama
出处
期刊:Microporous and Mesoporous Materials [Elsevier BV]
卷期号:333: 111726-111726 被引量:16
标识
DOI:10.1016/j.micromeso.2022.111726
摘要

The synthesis of zeolites without using an organic structure-directing agent (OSDA) offers great environmental and economic advantages; however, the zeolites being formed are not stabilized by the organic molecules and kinetic control of the synthesis ensuring high yield and purity of the phases is challenging for many zeolites. For OSDA-free synthesis of an Al-rich *BEA zeolite, this study shows that the zeolite is formed as a metastable phase that can undergo transformation immediately after completion of its crystallization to form a thermodynamically more stable MOR zeolite according to Ostwald's rule of stages. The OSDA-free zeolite synthesis is a dynamic process in which crystallization and dissolution occur simultaneously. As soon as a thermodynamically more stable MOR zeolite begins to form in the synthesis mixture, its formation causes depletion of the Al and Si from the synthesis mixture, and, because of the desaturation of the synthesis gel, the original *BEA zeolite begins to dissolve rapidly under hydrothermal conditions. The formation of targeted and parasitic zeolite structures is fundamentally affected by the Al and Si sources. Sources of Al and Si with suitable solubility and the presence of stable zeolite *BEA seeds allow kinetic control to direct the exclusive formation of *BEA zeolite up to a relatively high yields. Then, however, the MOR zeolite phase appears in the product and its formation becomes predominant. This study demonstrates the crucial importance of kinetic control for the selective formation of metastable zeolites in the OSDA-free synthesis.

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