Author:

Keywords:

G083318N#54518651, G0AC524N#57882052, I001321N#56241633, C14/22/099#57006169, WATUSO - 834134;info:eu-repo/grantAgreement/EC/H2020/834134, Science & Technology, Physical Sciences, Chemistry, Multidisciplinary, Crystallography, Chemistry, STRUCTURE-DIRECTING AGENTS, SOLVENT-FREE SYNTHESIS, CRYSTAL-STRUCTURE, CATION MIGRATION, THERMOCHEMISTRY, TEMPERATURE, ADSORPTION, PRECURSORS, FRAMEWORKS, STABILITY, NMRCORE, WATUSO, CMWS, 0302 Inorganic Chemistry, 0306 Physical Chemistry (incl. Structural), 0912 Materials Engineering, Inorganic & Nuclear Chemistry, 3402 Inorganic chemistry, 3403 Macromolecular and materials chemistry

Abstract:

Discovery of their commercial potential gave rise to a massive implementation of zeolites in industrial (petro-)chemical processes. Their robustness and molecular scale porosity in combination with acidic and/or ion exchange properties makes zeolites nearly indispensable for most of these applications. This highlight explores the origins of zeolite porosity. As microporosity is an inherent feature of the formed topology, we emphasize the link with phase selection. For zeolites, phase selection is driven by competition between water and framework elements to coordinate with extra-framework species and framework elements. This competition is important in the final product, where such coordinations provide thermodynamic stability, as well as in the crystallization medium where supermolecular structrures can play a templating role. Synthesis experiments using hydrated silicate ionic liquids show that limited water availability prompts the formation of less porous (or even dense) phases, while moderate hydration supports the development of more open frameworks. Understanding these interactions is key to deepening the insight into zeolite genesis and can guide strategies for tailoring material properties for industrial applications.