US EPA

4810627 

Journal Article 

Fischer-Tropsch synthesis: Effect of pretreatment conditions of cobalt on activity and selectivity for hydrogenation of carbon dioxide 

Gnanamani, MK; Jacobs, G; Keogh, RA; Shafer, WD; Sparks, DE; Hopps, SD; Thomas, GA; Davis, BH 

2015 

1 

Applied Catalysis A: General
ISSN: 0926-860X
EISSN: 1873-3875 

Elsevier 

499 

Elsevier 

39-46 

10.1016/j.apcata.2015.03.046 

WOS:000356209400005 

https://linkinghub.elsevier.com/retrieve/pii/S0926860X1500232X
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The effect of pretreatment conditions of cobalt on activity and product selectivity for the hydrogenation of carbon dioxide was studied over a 1%Na/20%Co SiO2 catalyst using a fixed-bed catalytic reactor operated at 220 degrees C and 1.89 MPa. The metallic form of cobalt was obtained from the reduction of cobalt oxide (CO3O4) by H-2 at 350 C and produced primarily methane and lower hydrocarbons (C-2-C-4) from CO2. Pretreatments with pure H-2 or syngas (H2 :CO) at 250 degrees C yield a fraction of partially reduced cobalt (COO), which tends to suppress the hydrogenation activity of cobalt somewhat, reducing methane selectivity to a limited degree. After CO activation, partially reduced cobalt oxide (CoO) and cobalt carbide phases formed and produced significantly less methane (i.e., selectivity of 15.3%), and surprisingly, the selectivity for alcohols increased to 73.2%. In the absence of sodium, direct methanation is still a preferred reaction for CO2 for CO pretreated cobalt: the XRD results of used catalysts revealed that the cobalt carbide phase converted to metallic cobalt. The results indicate that Na doping and carbide are important for low methane and high oxygenate selectivities. However, further work is needed to determine whether the role of Na is merely to stabilize the cobalt carbide phase, or whether Na is involved in promoting the catalytic cycle. (C) 2015 Elsevier B.V. All rights reserved. 

Carbon dioxide; Hydrogenation; Cobalt; Cobalt oxide; Cobalt carbide; Alcohols