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Fast room temperature lability of aluminosilicate zeolites

Author

Listed:
  • Christopher J. Heard

    (Charles University)

  • Lukas Grajciar

    (Charles University)

  • Cameron M. Rice

    (University of St Andrews)

  • Suzi M. Pugh

    (University of St Andrews)

  • Petr Nachtigall

    (Charles University)

  • Sharon E. Ashbrook

    (University of St Andrews)

  • Russell E. Morris

    (Charles University
    University of St Andrews)

Abstract

Aluminosilicate zeolites are traditionally used in high-temperature applications at low water vapour pressures where the zeolite framework is generally considered to be stable and static. Increasingly, zeolites are being considered for applications under milder aqueous conditions. However, it has not yet been established how neutral liquid water at mild conditions affects the stability of the zeolite framework. Here, we show that covalent bonds in the zeolite chabazite (CHA) are labile when in contact with neutral liquid water, which leads to partial but fully reversible hydrolysis without framework degradation. We present ab initio calculations that predict novel, energetically viable reaction mechanisms by which Al-O and Si-O bonds rapidly and reversibly break at 300 K. By means of solid-state NMR, we confirm this prediction, demonstrating that isotopic substitution of 17O in the zeolitic framework occurs at room temperature in less than one hour of contact with enriched water.

Suggested Citation

  • Christopher J. Heard & Lukas Grajciar & Cameron M. Rice & Suzi M. Pugh & Petr Nachtigall & Sharon E. Ashbrook & Russell E. Morris, 2019. "Fast room temperature lability of aluminosilicate zeolites," Nature Communications, Nature, vol. 10(1), pages 1-7, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-12752-y
    DOI: 10.1038/s41467-019-12752-y
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    Cited by:

    1. Andreas Erlebach & Martin Šípka & Indranil Saha & Petr Nachtigall & Christopher J. Heard & Lukáš Grajciar, 2024. "A reactive neural network framework for water-loaded acidic zeolites," Nature Communications, Nature, vol. 15(1), pages 1-14, December.

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