Related Experiment Video
Updated: Jun 7, 2025

Temperature-programmed Deoxygenation of Acetic Acid on Molybdenum Carbide Catalysts
Published on: February 7, 2017
Molybdenum Carbide Catalyst Enables Efficient Conversion of Chlorinated Volatile Organic Waste into Syngas through
Feng Lin1, Zezhi Chen1, Huijuan Gong1,2
1State Key Laboratory of Pollution Control and Resource Reuse, School of Environment, Nanjing University, Nanjing 210023, PR China.
Abstract:
Catalytic steam reforming offers a groundbreaking approach for converting industrial chlorinated volatile organic compound (CVOC) waste into valuable syngas (H2 and CO) and recovering HCl. However, the lack of C-Cl bond activation ability in traditional transition metal catalysts results in their insufficient reforming activity toward CVOCs. Herein, a novel molybdenum carbide (β-Mo2C) catalyst is developed and loaded onto a γ-Al2O3 support synthesized through a self-assembly method. The γ-Al2O3 support provides abundant unsaturated coordinated Al3+ ions, which effectively anchor and disperse β-Mo2C nanoparticles. In the catalytic steam reforming reaction at 600 °C, the β-Mo2C/γ-Al2O3 catalyst achieves a conversion efficiency higher than 95% and syngas yields of 82.4-92.3% for various typical industrial CVOCs. The mechanistic research reveals that the coordination between C and Mo atoms in β-Mo2C leads to a slightly electron-deficient state of the Mo sites, accompanied by a high density of unoccupied 4d orbitals. These characteristics are highly advantageous for the adsorption and dechlorination of CVOC molecules. The produced nonchlorinated intermediates can subsequently be oxidized to CO and H2 by hydroxyl radicals on adjacent Mo sites.
More Related Videos
10:57Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
Published on: April 10, 2018
07:47Reverse Microemulsion-mediated Synthesis of Monometallic and Bimetallic Early Transition Metal Carbide and Nitride Nanoparticles
Published on: November 27, 2015
Related Concept Videos
Alkenes via Reductive Coupling of Aldehydes or Ketones: McMurry Reaction
Reduction of Alkenes: Catalytic Hydrogenation
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Radical Substitution: Halogenation of Alkanes and Alkyl Substituents
In the initiation step of the reaction, the chlorine molecule undergoes homolytic cleavage in the presence of light or heat, forming two highly reactive chlorine radicals. Propagation occurs in two...
Olefin Metathesis Polymerization: Overview
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists...