Effect of Different Reaction Conditions on the Deactivation of Alumina-Supported Cobalt Fischer–Tropsch Catalysts in a Milli-Fixed-Bed Reactor: Experiments and Modeling

2014 ◽  
Vol 53 (17) ◽  
pp. 6913-6922 ◽  
Author(s):  
Majid Sadeqzadeh ◽  
Stéphane Chambrey ◽  
Jingping Hong ◽  
Pascal Fongarland ◽  
Francis Luck ◽  
...  
Author(s):  
Majid Sarkari ◽  
Farhad Fazlollahi ◽  
Hossein Atashi

The effects of K, Ce, Zn, Cs, and Rb promoters on the structure and catalytic behavior of precipitated 50%Fe/50%Mn catalyst in Fischer–Tropsch synthesis (FTS) were investigated in a fixed-bed reactor. The effects of promoter on Fischer-Tropsch iron catalysts caused an increased growth probability of hydrocarbon chains from 0.67 to 0.75 for K to Rb promoter, and the olefin/paraffin ratios increased from 0.99 to 1.36 for Rb to K-promoted catalyst. The effect on the olefin selectivity was certainly due to increased adsorption strength of CO causing an enhanced displacement of olefin. The catalysts were assessed in terms of their FTS activity and product selectivity using Anderson–Schulz–Flory (ASF) models. The effects of various reaction conditions such as flow rates, temperatures, and H2/CO feed ratios were studied and process synthesis concepts were used to investigate interactions between the optimum regions for reactor operation and the experimental results.


Author(s):  
Alba Mena Subiranas ◽  
Georg Schaub

The main objectives of the further downstream operations (product upgrading) of Fischer-Tropsch products are to i) improve yields and selectivities of the desired fractions, and ii) improve fuel properties to meet the fuel product specifications. The present study addresses the combination of low-temperature Fischer-Tropsch (FT) synthesis (with Co or Fe catalysts) and hydrocarbon modification reactions (hydroprocessing) in one reactor.In addition to earlier results with Pt/ZSM-5 in a dual-layer configuration in a fixed-bed reactor (Mena et al. 2007), the objective of the present investigation was to study the influence of CO during hydroprocessing and oligomerisation reactions of hydrocarbon model compounds (1-octene, ethene/propene) on two different bifunctional catalysts (Pt/ZSM-5, Pt/Beta). In addition, the influence of the catalyst-bed configuration for the combination FT synthesis and hydrocarbon reactions was investigated (dual layer/physical mixture).The achieved results indicate a potential of combining FT and hydrocarbons reactions in one reactor. Hydrogenation, isomerisation, cracking and oligomerisation reactions take place on a Pt/zeolite catalyst at FTS temperatures and in the presence of CO and H2O. The most critical point of this combination seems to be the deleterious effect of CO on the cracking reactions of isomers. For that reason, the wax fraction (C21+) was only partially cracked. The experimental results also indicate that the type of zeolite and the catalyst-bed configuration have an influence on the diesel/gasoline ratio obtained. It seems that the final fuel products will be a mixture of gasoline and diesel fuel and C1 to C5 compounds, as long as no diesel-selective hydroprocessing catalyst is found.


2012 ◽  
Vol 142 (11) ◽  
pp. 1382-1387 ◽  
Author(s):  
Dragomir B. Bukur ◽  
Zhendong Pan ◽  
Wenping Ma ◽  
Gary Jacobs ◽  
Burtron H. Davis

2021 ◽  
Vol 1 (1-2) ◽  
pp. 15
Author(s):  
Elham Yaghoobpour ◽  
Yahya Zamani ◽  
Saeed Zarrinpashne ◽  
Akbar Zamaniyan

Promoters and their loading amount have crucial roles in cobalt Fischer – Tropsch catalysts. In this regard, the effects of vanadium oxide (V2O5) as a proposed promoter for Co catalyst supported on TiO2 have been investigated. Three catalysts with 0, 1, and 3 wt.% of V2O5 promoter loading are prepared by the incipient wetness impregnation method, and characterized by the BET surface area analyzer, XRD, H2-TPR, and TEM techniques. The fixed-bed reactor was employed for their evaluations. It was found that the catalyst containing 1 wt.% V2O5 has the best performance among the evaluated catalysts, demonstrating remarkable selectivity: 92 % C5+ and 5.7 % CH4, together with preserving the amount of CO conversion compared to the unpromoted catalyst. Furthermore, it is reported that the excess addition of V2O5 promoter (> 1 wt.%) in the introduced catalyst leads to the detrimental effect on the CO conversion and C5+ selectivity, mainly owing to diminished active sites by V2O5 loading.


2020 ◽  
Vol 343 ◽  
pp. 156-164
Author(s):  
Nikola Nikačević ◽  
Branislav Todić ◽  
Miloš Mandić ◽  
Menka Petkovska ◽  
Dragomir B. Bukur

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