4.8 Article

Design of an intercalated Nano-MoS2 hydrophobic catalyst with high rim sites to improve the hydrogenation selectivity in hydrodesulfurization reaction

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 286, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.apcatb.2021.119907

Keywords

Ammonium exchange; Intercalation method; Hydrophobic; Monolayer; Pathway selectivity

Funding

  1. National Natural Science Foundation of China [21975285, U1862118, 21991091]
  2. Fundamental Research Funds for the Central Universities [20CX02203A]
  3. State Key Laboratory of Advanced Technology for Materials Synthesis and Processing (Wuhan University of Technology)
  4. National Key Research and Development Program of China [2017YFB0306600]

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By intercalating amine groups into nano-MoS2, the hydrophobic catalyst exhibited higher activity and selectivity in hydrodesulfurization reactions. The intercalated hydrophobic nano-MoS2 catalyst has increased number of active sites and shows good stability in catalytic cycles.
The preparation of the intercalated lamellar hydrophobic nano-MoS( )2 (size: 60-100 nm, interlayer spacing: 0.7-1.2 nm) through the substitution of organic amine for inorganic ammonium salt and the subsequent catalytic reaction as a hydrodesulfurization catalyst is presented. The intercalated amine groups broadened the interspacing of the lamellar nano-MoS2 and promoted the formation of hydrophobic stacking structure consisting of stable monolayers. The high hydrophobicity of the nano-MoS2 monolayer catalyst was confirmed. The assynthesized intercalated hydrophobic nano-MoS2 catalyst with lower steric hindrance and higher number of rim sites showed better hydrodesulfurization performance and higher hydrogenation mute selectivity than the traditional MoS2 catalyst. The conversion of dibenzothiophene using the intercalated hydrophobic nano-MoS2 catalyst was 86 % in comparison to 23 % for the traditional MoS2 catalyst. The intercalated hydrophobic nano-MoS2 catalyst was stable in five subsequent catalytic cycles.

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