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Propylene Metathesis over Molybdenum Silicate Microspheres with Dispersed Active Sites.

David ŠkodaRan ZhuBarbora HanulikovaAles StyskalikVit VykoukalPetr MachacLucie SimonikovaIvo KuritkaClaude PoleunisDamien P DebeckerYuriy Roman-Leshkov
Published in: ACS catalysis (2023)
In this work, we demonstrate that amorphous and porous molybdenum silicate microspheres are highly active catalysts for heterogeneous propylene metathesis. Homogeneous molybdenum silicate microspheres and aluminum-doped molybdenum silicate microspheres were synthesized via a nonaqueous condensation of a hybrid molybdenum biphenyldicarboxylate-based precursor solution with (3-aminopropyl)triethoxysilane. The as-prepared hybrid metallosilicate products were calcined at 500 °C to obtain amorphous and porous molybdenum silicate and aluminum-doped molybdenum silicate microspheres with highly dispersed molybdate species inserted into the silicate matrix. These catalysts contain mainly highly dispersed MoO x species, which possess high catalytic activity in heterogeneous propylene metathesis to ethylene and butene. Compared to conventional silica-supported MoO x catalysts prepared via incipient wetness impregnation (MoIWI), the microspheres with low Mo content (1.5-3.6 wt %) exhibited nearly 2 orders of magnitude higher steady-state propylene metathesis rates at 200 °C, approaching site time yields of 0.11 s -1 .
Keyphrases
  • highly efficient
  • metal organic framework
  • molecularly imprinted
  • quantum dots
  • transition metal
  • mass spectrometry