A facile one‐pot hydrothermal method is developed to synthesize a series of carbon nanotubes–manganese oxide nanocomposites (CNTs–MnOx) with different morphologies and Mn valence states. These nanocomposite materials are then utilized as catalyst supports in iron‐based Fischer–Tropsch synthesis (FTS) for the production of liquid fuels. Experimental results indicate that Fe/CNTs‐K‐190 (iron catalyst supported on the CNTs treated with KMnO4 at 190 °C) and Fe/CNTs‐KU‐190 (iron catalyst supported on the CNTs treated with KMnO4 and urea at 190 °C) display higher FTS activity than the Fe/CNTs‐K‐110 (iron catalyst supported on CNTs treated with KMnO4 at 110 °C) and Fe/CNTs‐KU‐110 (iron catalyst supported on CNTs treated with KMnO4 and urea at 110 °C). This might be due to the weak metal–support interaction and high MnO content, and the poorer stability than Fe/CNTs‐K‐110 and Fe/CNTs‐KU‐110 catalysts with nanosheet morphology might be related to the structural collapse of the nanocubes or nanorods due to MnO evolution during the FTS process. The CNTs–MnOx nanocomposite‐supported iron FTS catalysts in particular display unparalleled high C5+ selectivity (over 90 %) and very low CH4 selectivity (below 4.6 %). The unique CNTs–MnOx nanocomposites may open a new window for the understanding, design, synthesis, and optimization of iron catalysts toward high‐efficiency transport fuel production.
Titanium silicalite (TS) and TiO2 nanocomposites were prepared by mixing TS and TiO2 with different ratios in ethanol. They were impregnated with 15 wt% Co loading to afford Co‐based catalysts. Fischer–Tropsch synthesis (FTS) performance of these TS–TiO2 nanocomposite‐supported Co‐based catalysts was studied in a fixed‐bed tubular reactor. The results reveal that the Co/TS–TiO2 catalysts have better catalytic performance than Co/TS or Co/TiO2 each with a single support, showing the synergistic effect of the binary TS–TiO2 support. Among the TS–TiO2 nanocomposite‐supported Co‐based catalysts, Co/TS–TiO2‐1 presents the highest activity. These catalysts were characterized using N2 adsorption–desorption measurements, X‐ray diffraction, X‐ray photoelectron spectroscopy, H2 temperature‐programmed reduction, H2 temperature‐programmed desorption and transmission electron microscopy. It was found that the position of the active component has a significant effect on the catalytic activity. In the TS–TiO2 nanocomposites, cobalt oxides located at the new pores developed between TS and TiO2 can exhibit better catalytic activity. Also, a positive relationship is observed between Co dispersion and FTS catalytic performance for all catalysts. The catalytic activity is improved on increasing the dispersion of Co.
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