| Home > Publications database > The enhancing effect of Co$^{2+}$ on propane non-oxidative dehydrogenation over supported Co/ZrO$_2$ catalysts |
| Journal Article | PUBDB-2024-01186 |
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2024
Elsevier
Amsterdam [u.a.]
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Please use a persistent id in citations: doi:10.1016/j.jcat.2024.115440 doi:10.3204/PUBDB-2024-01186
Abstract: Due to the increased production of shale gas containing propane, the share of non-oxidative propane dehydrogenation (PDH) in the large-scale production of propene is expected to continue to grow. There are, however, some ecofriendly and cost shortcomings associated with the currently applied Cr- or Pt-containing catalysts. Against this background, we present here Co/ZrO$_2$ alternatives and reveal the fundamentals affecting their activity, which can be used for purposeful catalyst design. Co$^{2+}$ species homogeneously distributed within the lattice of ZrO$_2$ significantly increase the activity of coordinatively unsaturated Zr$^{4+}$ for the PDH reaction. The increase is caused by accelerating both the cleavage of CH bonds in propane and the recombination of surface H species, with the latter reaction being the rate-limiting step. The best-performing catalyst outperformed an analogue of commercial K-CrO$_x$/Al$_2$O$_3$ in terms of the rate of propene formation and demonstrated durable performance over a series of 10 PDH/regeneration cycles under industrially relevant conditions. It also outperformed most previously developed Co-containing catalysts in terms of propene productivity. The space–time yield of propene formation achieved at 57 % equilibrium propane conversion at 550 °C was 0.71 kg·h$^{−1}$·kg$_{cat}$$^{-1}$.
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