Development of Highly Active Silica-Supported Nickel Phosphide Catalysts for Direct Dehydrogenative Conversion of Methane to Higher Hydrocarbons

2021 ◽  
Author(s):  
Arnoldus Lambertus Dipu ◽  
Yuta Nishikawa ◽  
Yuta Inami ◽  
Shoji Iguchi ◽  
Ichiro Yamanaka
ACS Catalysis ◽  
2019 ◽  
Vol 10 (1) ◽  
pp. 375-379 ◽  
Author(s):  
Arnoldus Lambertus Dipu ◽  
Shunya Ohbuchi ◽  
Yuta Nishikawa ◽  
Shoji Iguchi ◽  
Hitoshi Ogihara ◽  
...  

1989 ◽  
Vol 42 (10) ◽  
pp. 1655 ◽  
Author(s):  
FP Larkins ◽  
AZ Khan

Some basic thermodynamic parameters such as Gibbs free energies, enthalpies of reactions and equilibrium compositions of products from the pyrolysis and partial oxidation of methane to higher hydrocarbons in the gas phase have been determined within a consistent framework for the temperature range 800-1500 K and the pressure range 0.1-3 MPa , by using the CSIRO-SGTE THERMODATA system. It has been established that the pyrolysis of methane to higher hydrocarbons, e.g. acetylene, ethylene, ethane, prop-1-ene, propane, benzene, toluene, naphthalene, 1-methylnaphthalene and 2-methylnaphthalene, considered as separate reactions, is a highly endothermic reaction with the Gibbs free energies for the individual reactions being positive until 1300 K. The aromatics are thermodynamically most favoured with the equilibrium yields increasing with temperature. Addition of O2 lowers the heats of synthesis and the free energies for methane conversion but no enhancement in the equilibrium yields of hydrocarbons is observed. When solid carbon is allowed, it is the dominant product in all cases with the equilibrium yields for all hydrocarbons becoming negligible. Increasing the pressure at a particular temperature has more effect on the lowering of the equilibrium conversion of methane than on the suppression of solid carbon. Such data are valuable for understanding the conversion limits for methane into higher hydrocarbons.


1987 ◽  
Vol 5 (2) ◽  
pp. 169-183 ◽  
Author(s):  
Prasad S. Yarlagadda ◽  
Lawrence A. Morton ◽  
Norman R. Hunter ◽  
Hyman D. Gesser

2013 ◽  
Vol 31 (3) ◽  
pp. 481-486 ◽  
Author(s):  
H.A. Navid ◽  
E. Irani ◽  
R. Sadighi-Bonabi

AbstractConversion of CH4molecule into higher hydrocarbons using two different wavelengths of 248 nm KrF laser and 355 nm of third harmonic of Nd:YAG laser is studied experimentally and theoretically. The stable products are analyzed and the effect of pressure on conversion of methane is measured. The detected reaction products are C2H2, C2H4, and C2H6. The conversion efficiency of 33.5% for 355 nm in comparison to 2.2% conversion for 248 nm for C2H2is achieved. The potential of laser parameters as an important variable in controlling of final products is investigated.


2017 ◽  
Vol 129 (11) ◽  
pp. 1705-1711 ◽  
Author(s):  
Sourabh Mishra ◽  
Sonit Balyan ◽  
Kamal K Pant ◽  
M Ali Haider

1991 ◽  
Vol 69 (1) ◽  
pp. 37-42 ◽  
Author(s):  
Alain R. Bossard ◽  
Margaret H. Back

Mixtures of ethylene and methane have been pyrolyzed in the temperature range 925–1023 K for the purpose of converting methane to higher hydrocarbons. Addition of methane to thermally-reacting ethylene increases the rate of formation of propylene but decreases the rates of formation of the other major products, ethane, acetylene, and butadiene. Hydrogen abstraction from methane is a major propagation reaction and causes a shift in the radical distribution from ethyl and vinyl radicals, the main radicals in the pyrolysis reactions of ethylene alone, to methyl radicals, which lead to the formation of propylene. At 1023 K with a pressure of ethylene of 6.5 Torr and of methane of 356 Torr, 1.5 mol of methane is converted to higher molecular weight products for every mole of ethylene reacted. The rate of conversion of methane in the homogeneous system is lower than in catalytic reactions but the product is entirely hydrocarbon and no methane is lost to carbon monoxide or carbon dioxide. Key words: methane, ethylene, kinetics, pyrolysis, fuels.


2016 ◽  
Vol 335 ◽  
pp. 204-214 ◽  
Author(s):  
Andrea I. d’Aquino ◽  
Samuel J. Danforth ◽  
Tess R. Clinkingbeard ◽  
Boris Ilic ◽  
Lee Pullan ◽  
...  

2003 ◽  
Vol 36 (4) ◽  
pp. 313-326 ◽  
Author(s):  
M. A. Gondal ◽  
Zain H. Yamani ◽  
A. Dastgeer ◽  
M. A. Ali ◽  
A. Arfaj

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