Cobalt Carbonyl Cluster as Catalyst Precursor for Fischer-Tropsch Synthesis

2011 ◽  
Vol 236-238 ◽  
pp. 684-688
Author(s):  
Feng Hua Bai ◽  
Yin Xia Zhang ◽  
Hai Quan Su ◽  
Xue Fen Li ◽  
Hui Pan ◽  
...  

The effect of precursors of Co/γ-Al2O3 catalysts prepared from Co(NO3)2 and (CO)6Co2CC(COOH)2 on the Fischer-Tropsch synthesis (FTS) catalytic performance were investigated. All catalysts were characterised by TGA, BET, pore size distribution analysis and TEM techniques. For Aluminium-supported catalyst, the use of cobalt carbonyl cluster as cobalt precursor resulted in a higher activity and C5+ selectivities compared with the reference catalyst prepared from nitrate at low reaction temperature. The activities can be correlated with the zero valent cobalt metal exist on the support. The chain growth attribute to well dispersed smaller metallic cobalt particles resulted from the partial removal of terminal carbonyls at 150°C.

2017 ◽  
Vol 17 (43) ◽  
pp. 38-41
Author(s):  
Byambasuren O ◽  
Ulziibayar D ◽  
Chiibaatar D

On 3rd March 2018, the Editorial Board of the Mongolian Journal of Chemistry decided to retract the article entitled "Effect of pretreatment temperature on catalytic performance of the catalysts derived from cobalt carbonyl cluster in Fischer-Tropsch Synthesis" because of an authorship dispute. The article was originally published in Vol.17 No.43 2016 pp.38-41. DOI: http://dx.doi.org/10.5564/mjc.v17i43.745


2018 ◽  
Vol 18 (44) ◽  
Author(s):  
Byambasuren O ◽  
Ulziibayar D ◽  
Chiibaatar D

On 3rd March 2018, the Editorial Board of the Mongolian Journal of Chemistry decided to retract the article entitled "Effect of pretreatment temperature on catalytic performance of the catalysts derived from cobalt carbonyl cluster in Fischer-Tropsch Synthesis" because of an authorship dispute. The article was originally published in Vol.17 No.43 2016 pp.38-41. DOI: http://dx.doi.org/10.5564/mjc.v17i43.745


2011 ◽  
Vol 346 (1-2) ◽  
pp. 55-69 ◽  
Author(s):  
Dong-Bo Cao ◽  
Yong-Wang Li ◽  
Jianguo Wang ◽  
Haijun Jiao

2017 ◽  
Vol 682 ◽  
pp. 115-121 ◽  
Author(s):  
Yifan Wang ◽  
Ying Li ◽  
Shouying Huang ◽  
Jian Wang ◽  
Hongyu Wang ◽  
...  

Author(s):  
Luis A. Díaz-Trujillo ◽  
Gilberto Toledo-Chávez ◽  
Gladys Jiménez-García ◽  
Héctor Hernández-Escoto ◽  
Rafael Maya-Yescas

AbstractThe main goal of this paper is to critically review current microkinetics available for Fischer-Tropsch synthesis (FTS) modelling, in order to propose the best way to follow this set of complex reactions; therefore a microkinetic model was developed for FTS, accomplishing surface chemistry, heterogeneous kinetics, and single-event previous development for Co-based catalysts. Model starts simulating CO activation on catalyst surface, and then formation of methane, ethane and subsequent chain growth. Reaction rates were derived following the formalism of Langmuir-Hinshelwood-Hougen-Watson (LHHW); surface steps were proposed in consequence of feasibility. Chain growth was modelled by single-event steps, taking into account geometrical conformation explicitly. Number of growth steps of 1-olefins was rectified as requiring one more active site than mechanisms proposed previously; it was found that formation of these olefins exhibits a fast drop in chain growth; this phenomenon is explained in terms of probable geometrical conformations that lead to the number of single events. Experimental results in literature about isothermal synthesis of hydrocarbons in the gasoline range were simulated in a fixed-bed laboratory reactor; thermodynamic consistency was derived from chemical equilibrium over all reactions occurring during FTS. Equilibrium constants were evaluated as function of Gibbs free energy, and partial pressures of reactants and products.


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