Mayenite-Based Electride C12A7e−: A Reactivity and Stability Study

  • Sebastian Weber
    hte GmbH, Kurpfalzring 104, 69123 Heidelberg, Germany
  • Sebastian Schäfer
    hte GmbH, Kurpfalzring 104, 69123 Heidelberg, Germany
  • Mattia Saccoccio
    hte GmbH, Kurpfalzring 104, 69123 Heidelberg, Germany
  • Nils Ortner
    Leibniz Institute for Catalysis (LIKAT Rostock), Albert-Einstein-Straße 29a, 18059 Rostock, Germany
  • Marko Bertmer
    Felix-Bloch-Institut für Festkörperphysik, Leipzig University, Linnéstraße 5, 04103 Leipzig, Germany
  • Karsten Seidel
    BASF SE, Carl-Bosch-Straße 38, 67056 Ludwigshafen am Rhein, Germany
  • Stefan Berendts
    Institute of Chemistry, TU Berlin, Straße des 17. Juni 135, 10623 Berlin, Germany
  • Martin Lerch
    Institute of Chemistry, TU Berlin, Straße des 17. Juni 135, 10623 Berlin, Germany
  • Roger Gläser
    Institute of Chemical Technology, Leipzig University, Linnéstraße 3, 04103 Leipzig, Germany
  • Holger Kohlmann
    Institute of Inorganic Chemistry, Leipzig University, Johannisallee 29, 04103 Leipzig, Germany
  • Stephan A. Schunk
    hte GmbH, Kurpfalzring 104, 69123 Heidelberg, Germany

Description

<jats:p>Ru supported on mayenite electride, [Ca24Al28O64]4+(e−)4 a calcium aluminum oxide denoted as C12A7e−, are described in the literature as highly active catalysts for ammonia synthesis, especially under conditions of low absolute pressure. In this study, we investigated the application of recently reported plasma arc melting synthesized C12A7e− (aluminum solid reductant) as supports of Ru/C12A7e− catalysts in ammonia synthesis up to pressures of 7.6 MPa. Together with the plasma-arc-melting-based catalyst support, we investigated a similar plasma-synthesized C12A7e− (graphite solid reductant) and a vacuum-sintering-based C12A7e−. Complementary to the catalytic tests, we applied 2H solid-state NMR spectroscopy, DRUVVis-spectroscopy, thermal analysis and PXRD to study and characterize the reactivity of different plasma-synthesized and vacuum-sintered C12A7e− towards H2/D2 and H2O. The catalysts showed an immediate deactivation at pressures > 1 MPa, which can be explained by irreversible hydride formation at higher pressures, as revealed by reactivity tests of C12A7e− towards H2/D2. The direct formation of C12A7:D from C12A7e− is proven. It can be concluded that the application of Ru/C12A7e− catalysts at the industrial scale has limited prospects due to irreversible hydride formation at relevant pressures > 1 MPa. Furthermore, we report an in-depth study relating to structural changes in the material in the presence of H2O.</jats:p>

Journal

  • Catalysts

    Catalysts 11 (3), 334-, 2021-03-05

    MDPI AG

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