Hydrogen from Formic Acid via Its Selective Disproportionation over Nanodomain-Modified Zeolites

Ruth I.J. Amos*, Falk Heinroth, Bun Chan, Antony J. Ward, Sisi Zheng, Brian S. Haynes, Christopher J. Easton, Anthony F. Masters, Thomas Maschmeyer, Leo Radom

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    14 Citations (Scopus)

    Abstract

    Sodium germanate is a nontransition-metal catalyst that is active in the selective dehydrogenation of formic acid. However, bulk sodium germanate has a very low surface area, limiting the availability of the germanate sites for catalysis. The dispersion of germanate in the zeolite ZSM-5 has been investigated both computationally and experimentally as a method for the provision of greater surface area and, therefore, higher activity per germanate site. Nanodomain islets of germanate dispersed in the germanium ZSM-5 zeolite invert selectivity from dehydration (in ZSM-5) to dehydrogenation of formic acid, potentially making Na-Ge-ZSM-5 a cost-effective catalyst for releasing hydrogen from formic acid.

    Original languageEnglish
    Pages (from-to)4353-4362
    Number of pages10
    JournalACS Catalysis
    Volume5
    Issue number7
    DOIs
    Publication statusPublished - 18 Jun 2015

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