4.2 Article

A zeolite crystallisation model confirmed by in situ observation

期刊

FARADAY DISCUSSIONS
卷 235, 期 -, 页码 162-182

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ROYAL SOC CHEMISTRY
DOI: 10.1039/d1fd00093d

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资金

  1. Austrian COMET-K2 program [I3680-N34]
  2. FWO [1.5.061.18N, G083318N]
  3. Flemish Methusalem program - European Research Council (ERC)
  4. [834134]

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This study investigated zeolite crystallization from single phasic hydrated silicate ionic liquids (HSiL) using a specifically designed conductivity measurement set-up, providing access to the crystallization kinetics. A crystallization model based on a surface growth mechanism was proposed, showing that zeolite crystallization from highly ionic media proceeds via a multi-step mechanism involving reversible surface condensation and incorporation of growth units into the crystal. The agreement between experiment and theory suggests that the crystallization process is governed by liquid phase concentration, surface energy, and cation mobility.
Probing nucleation and growth of porous crystals at a molecular level remains a cumbersome experimental endeavour due to the complexity of the synthesis media involved. In particular, the study of zeolite formation is hindered as these typically form in multiphasic synthesis media, which restricts experimental access to crystallisation processes. Zeolite formation from single phasic hydrated silicate ionic liquids (HSiL) opens new possibilities. In this work, HSiL zeolite crystallisation is investigated in situ using a specifically designed conductivity measurement set-up yielding access to crystallisation kinetics. Based on the conductivity data and final yields, a crystallisation model explaining the results based on a surface growth mechanism was derived. The excellent agreement between experiment and theory indicates zeolite crystallisation from highly ionic media proceeds via a multi-step mechanism, involving an initial reversible surface condensation of a growth unit, followed by incorporation of that unit into the growing crystal. The first step is governed by the liquid phase concentration and surface energy, while the final step shows a correlation to the mobility of the cation involved.

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