Thermal stability and hcp–fcc allotropic transformation in supported Co metal catalysts probed near operando by ferromagnetic NMR

2015 ◽  
Vol 17 (22) ◽  
pp. 14598-14604 ◽  
Author(s):  
Andrey S. Andreev ◽  
Jean-Baptiste d'Espinose de Lacaillerie ◽  
Olga B. Lapina ◽  
Alexander Gerashenko

Ferromagnetic NMR reveals which cobalt metallic phase is actually at work in Fischer–Tropsch catalysts and what is its state of dispersion under operando conditions.

2020 ◽  
Vol 130 (2) ◽  
pp. 813-823
Author(s):  
Mariia E. Markova ◽  
Alexandra V. Gavrilenko ◽  
Antonna A. Stepacheva ◽  
Valentina G. Matveeva ◽  
Mikhail G. Sulman ◽  
...  

Author(s):  
I. V. Derevich ◽  
V. S. Ermolaev ◽  
V. Z. Mordkovich

Investigation of oscillation of temperature and synthesis gas concentration inside spherical catalytic particle it is executed. Approximate distributions of temperature and concentrations in a particle with internal heat release and synthesis gas consumption are obtained. Stationary distributions of thermal and gaseous parameters are found. In the frame of small disturbances of temperature and concentrations thermal stability is investigated. It is revealed, that diffusion resistance synthesis gas inside a porous particle can lead to occurrence oscillation regime.


Author(s):  
Jennifer Lindsey Suder Klettlinger

Fischer-Tropsch (F-T) jet fuel composition differs from petroleum-based, conventional commercial jet fuel because of differences in feedstock and production methodology. Fischer-Tropsch fuel typically has a lower aromatic and sulfur content and consists primarily of iso and normal parafins. The ASTM D3241 specification for Jet Fuel Thermal Oxidation Test (JFTOT) break point testing method was used to test the breakpoint of a baseline commercial grade F-T jet fuel, and various blends of this F-T fuel with an aromatic solution. The goal of this research is to determine the effect of aromatic content on the thermal stability of Fischer-Tropsch fuel. The testing completed in this report was supported by the NASA Fundamental Aeronautics Subsonics Fixed Wing Project.


2020 ◽  
Vol 42 ◽  
pp. e45899
Author(s):  
Lidiane Sabino da Silva ◽  
Gabriela Gonzaga Cher ◽  
Maria Auxiliadora Scaramelo Baldanza ◽  
Victor Luis dos Santos Teixeira da Silva ◽  
Pedro Augusto Arroyo

 In the present work, the synthesis of Co/SBA-15 catalysts intended for Fischer-Tropsch (FT) synthesis was performed. During the synthesis of catalysts there was contamination of samples with sodium nitrate due to the nature of the reducing agent used for the synthesis of metallic phase. This kind of impurity is not advantageous for the FT reaction. Attempts at removal of sodium compounds were carried out by means of simple leaching treatments, using ethanol and acid ethylenediaminetetraacetic (EDTA) as solvent and complexing agent, respectively, followed by heat treatment at temperatures of 150 or 300°C. It was possible to conclude that the treatment using EDTA was more effective in removing almost all the alkaline phase of samples, despite the occurrence of oxidation, agglomeration, and removal of the metal nanoparticles in this process. In addition, there were no significant differences in the product selectivity of FT synthesis of the catalysts after sodium removal, although the nanoparticles were larger than 10 nm.


2019 ◽  
Vol 26 (1) ◽  
pp. 137-144 ◽  
Author(s):  
Chandrani Nayak ◽  
Preeti Jain ◽  
C. P. Vinod ◽  
S. N. Jha ◽  
D. Bhattacharyya

This article describes the setting up of a facility on the energy-scanning EXAFS beamline (BL-09) at RRCAT, Indore, India, for operando studies of structure–activity correlation during a catalytic reaction. The setup was tested by operando X-ray absorption spectroscopy (XAS) studies performed on a Co-based catalyst during the Fischer–Tropsch reaction to obtain information regarding structural changes in the catalyst during the reaction. Simultaneous gas chromatography (GC) measurements during the reaction facilitate monitoring of the product gases, which in turn gives information regarding the activity of the catalyst. The combination of XAS and GC techniques was used to correlate the structural changes with the activity of the catalyst at different reaction temperatures. The oxide catalyst was reduced to the metallic phase by heating at 400°C for 5 h under H2 at ambient pressure and subsequently the catalytic reaction was studied at four different temperatures of 240, 260, 280 and 320°C. The catalyst was studied for 10 h at 320°C and an attempt has been made to understand the process of its deactivation from the XANES and EXAFS results.


2021 ◽  
pp. 116604
Author(s):  
Lizandra M.N.C. Alves ◽  
Mayra P. Almeida ◽  
Martin Ayala ◽  
Caleb D. Watson ◽  
Gary Jacobs ◽  
...  

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