Diverse Physical States of Amorphous Precursors in Zeolite Synthesis

成核 结晶 沸石 微型多孔材料 硅酸铝 无定形固体 化学工程 材料科学 纳米技术 化学 有机化学 催化作用 工程类
作者
Rui Li,Aseem Chawla,Noemi Linares,James G. Sutjianto,Karena W. Chapman,Javier García‐Martínez,Jeffrey D. Rimer
出处
期刊:Industrial & Engineering Chemistry Research [American Chemical Society]
卷期号:57 (25): 8460-8471 被引量:57
标识
DOI:10.1021/acs.iecr.8b01695
摘要

The assembly and structural evolution of amorphous precursors during zeolite crystallization is an important area of interest owing to their putative roles in the nucleation and growth of aluminosilicate microporous materials. Precursors range in complexity from oligomeric molecules and colloidal particles to gels comprised of heterogeneous silica and alumina domains. The physical state of precursors in most zeolite syntheses is generally not well understood; however, it is evident that the physicochemical properties of precursors depend on a wide range of conditions that include (but are not limited to) the selection of reagents, the composition of growth mixtures, the methods of preparation, and the use of inorganic and/or organic structure-directing agents. The fact that precursors evolve in size, shape, and/or microstructure during the course of nucleation and potentially throughout crystallization leads to questions pertaining to their mode of action in the formation of zeolites. This also highlights the diversity of species that are present in growth media, thus rendering the topic of zeolite synthesis essentially a black box to those attempting to better understand the fundamental role(s) of precursors. In this Article, we discuss the wide variety of precursors encountered in the synthesis of various framework types, emphasizing their complex physical states and the thermodynamic and kinetic factors that govern their heterogeneity.
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