Supported Molybdenum Carbide Catalysts: Structure-Function Relationships for Hydrodenitrogenation

1996 ◽  
Vol 454 ◽  
Author(s):  
Gregory M. Dolce ◽  
Levi T. Thompson

ABSTRACTEarly transition metal carbides and nitrides have been shown to be active for the hydrotreatment of model compounds and petroleum crudes. In this paper we describe our investigations of the structural and compositional properties of γ-Al2O3-supported molybdenum carbides and efforts to correlate these properties with their pyridine and quinoline hydrodenitrogenation (HDN) activities. The HDN activities of the materials scaled linearly with the loading and oxygen chemisorptive uptake. Oxygen chemisorption results also suggested that the molybdenum carbide particles were highly dispersed and perhaps raft-like. Using temperature programmed desorption and infrared spectroscopy of carbon monoxide, we were able to identify two types of sites on the carbides; sites “on top” of the particle and sites at the perimeter. We have tentatively concluded that the most active sites for HDN were “on top” of the supported carbide particles.

2017 ◽  
Vol 5 (17) ◽  
pp. 7764-7768 ◽  
Author(s):  
Rajinder Kumar ◽  
Ritu Rai ◽  
Seema Gautam ◽  
Abir De Sarkar ◽  
Nidhi Tiwari ◽  
...  

A highly efficient, low-cost (precious-metal-free), highly stable nanohybrid electrocatalyst containing carbon-supported molybdenum carbide and nitride nanoparticles of size ranging from 8 to 12 nm exhibit excellent HER catalytic activity.


Author(s):  
Yanlong Lv ◽  
Jian Ru Gong

The design of a universal synthesize strategy of long-term durable transition metal carbides catalysts with controllable nanostructure and sufficient active sites for hydrogen evolution reaction is challenging. Herein, the in-situ...


ChemSusChem ◽  
2012 ◽  
Vol 5 (4) ◽  
pp. 727-733 ◽  
Author(s):  
Junxing Han ◽  
Jinzhao Duan ◽  
Ping Chen ◽  
Hui Lou ◽  
Xiaoming Zheng ◽  
...  

2021 ◽  
Author(s):  
Kushagra Agrawal ◽  
Alberto Roldan ◽  
Nanda Kishore ◽  
Andrew J Logsdail

The decomposition of formic acid is investigated on the β-Mo<sub>2</sub>C (100) catalyst surface using density functional theory. The dehydration and dehydrogenation mechanism for the decomposition is simulated, and the thermochemistry and kinetics are discussed. The potential energy landscape of the reaction shows a thermodynamically favourable cleavage of H-COOH to form CO; however, the kinetics show that the dehydrogenation mechanism is faster and CO<sub>2</sub> is continuously formed. The effect of HCOOH adsorption on the surface is also analysed, in a temperature-programmed reaction, with the decomposition proceeding at under 350 K and desorption of CO<sub>2</sub> observed.


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