Microwave modification of iron supported on beta silicon carbide catalysts for Fischer–Tropsch synthesis
Literature Information
Christel Olivier Lenge Mbuya, Chike George Okoye-Chine, Katu Ramutsindela, Linda L. Jewell, Mike Scurrell
This research article investigated the microwave modification of iron supported on beta silicon carbide catalysts (Fe/β-SiC) for Fischer–Tropsch synthesis (FTS). The surface area of the Fe/β-SiC catalyst was not affected by a 15 second (s) exposure to microwave irradiation (MIR) but a slight increase was observed for a 20 s, 25 s, and 30 s MIR exposure. The elemental mapping and XPS results showed a decrease in the silicon (Si) percentage on the Fe/β-SiC catalyst's surface when exposed to MIR. This would be beneficial for the FTS since there will be fewer iron silicate species that are considered inactive for Fe FTS catalysts. Because of the weak Fe and β-SiC interaction, a decrease in the reduction temperature peaks of the Fe/β-SiC catalysts which were exposed to MIR was observed without the use of chemical promoters. As a result, we observed a positive effect of MIR on the CO conversion after 20 s and 25 s exposure times. Meanwhile, the 30 second exposure to MIR was detrimental to the Fe/β-SiC catalyst. Despite the increase in the CO conversion, we also observed an increase in CH4 selectivity with increasing MIR time.
Recommended Journals

Critical Reviews in Solid State and Materials Sciences

Topics in Catalysis

Journal of the Indian Institute of Science

Journal of Chemical Sciences

Colloid Journal

Biocatalysis and Biotransformation

NDT & E International

Acta Metallurgica Sinica-English Letters

Medicinal Chemistry Research

Journal of Asian Natural Products Research
Related Literature
Comparative analysis of ethanol dynamics in aqueous and non-aqueous solutions
Ivo Jukić, Martina Požar, Bernarda Lovrinčević
DOI: 10.1039/D0CP03160G
Analysis of thyme essential oils using gas-phase broadband rotational spectroscopy
DOI: 10.1039/C9CP05583E
Unraveling the regioselectivity of odd electron halogen bond formation using electrophilicity index and chemical hardness parameters
Prasanta Bandyopadhyay, Soumyadip Ray, Md. Motin Seikh
DOI: 10.1039/C9CP05374C
Theoretical insights on acceptor–donor dyads for organic photovoltaics
Domenico Alberga, Ilaria Ciofini
DOI: 10.1039/D0CP03038D
Does addition of 1-octanol as a phase modifier provide radical scavenging radioprotection for N,N,N′,N′-tetraoctyldiglycolamide (TODGA)?
Gregory P. Horne, Christopher A. Zarzana, Cathy Rae, Andrew R. Cook, Stephen P. Mezyk, Peter R. Zalupski, Andreas Wilden, Bruce J. Mincher
DOI: 10.1039/D0CP04310A
DNA-binding mechanisms of human and mouse cGAS: a comparative MD and MM/GBSA study
Honghui Zhang, Wenjin Li
DOI: 10.1039/D0CP04162A
Free volume, gas permeation, and proton conductivity in MIL-101-SO3H/Nafion composite membranes
Chongshan Yin, Chunqing He, Qicheng Liu, Bangyun Xiong, Xiaowei Zhang, Libing Qian, Jingjing Li, Yawei Zhou
DOI: 10.1039/C9CP04832D
Simple thiophene-bridged D–π–A type chromophores for DSSCs: a comprehensive study of their sensitization and co-sensitization properties
Kavya S. Keremane, Islam M. Abdellah, Praveen Naik, Ahmed El-Shafei
DOI: 10.1039/D0CP02781B
You might also like
How should waste containing 2-Ethyl-4-Methyl-1H-Imidazole-5-Carbaldehyde (CAS: 88634-80-4) be handled?
Waste containing 2-Ethyl-4-Methyl-1H-Imidazole-5-Carbaldehyde (CAS: 88634-80-4) ...
What industries use Triethoxy(octyl)silane (CAS: 1385031-14-0)?
Triethoxy(octyl)silane (CAS: 1385031-14-0) is widely used in the pharmaceuticals...
Are there alternatives to 3-iodo-7-nitro-1H-indazole (CAS: 864724-64-1) in synthesis?
Several alternatives to 3-iodo-7-nitro-1H-indazole (CAS: 864724-64-1) exist in t...
Are there alternatives to Benzene, bis[(trimethoxysilyl)ethyl] (CAS: 266317-71-9) in synthesis?
Yes, there are alternatives to Benzene, bis[(trimethoxysilyl)ethyl] (CAS: 266317...
Is Isothiazole-3-carbonitrile (CAS: 1452-17-1) safe?
Isothiazole-3-carbonitrile (CAS: 1452-17-1) is generally considered safe when us...
Is (3-Chlorophenyl)methanol (CAS: 873-63-2) safe?
(3-Chlorophenyl)methanol (CAS: 873-63-2) is considered low to moderately toxic. ...
How is (2S,3S)-2-Hydroxy-3-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-3-(2-naphthyl)propanoic acid (CAS: 959583-98-3) typically synthesized?
(2S,3S)-2-Hydroxy-3-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-3-(2-naphthyl)pr...
What precautions should be taken when handling Methyl 2-(bromomethyl)-5-methoxybenzoate (CAS: 788081-99-2)?
Proper handling of methyl 2-(bromomethyl)-5-methoxybenzoate requires the use of ...
What is 6,8-Dibromoimidazo[1,2-a]pyridine-2-carboxylic acid (CAS: 904805-36-3)?
6,8-Dibromoimidazo[1,2-a]pyridine-2-carboxylic acid (CAS: 904805-36-3) is an aro...
Is 3-Amino-5-bromo-2-pyridinecarbonitrile (CAS: 573675-27-1) safe?
3-Amino-5-bromo-2-pyridinecarbonitrile is considered safe when handled under pro...
Source Journal
Reaction Chemistry & Engineering

Reaction Chemistry & Engineering is an interdisciplinary journal reporting cutting-edge research focused on enhancing the understanding and efficiency of reactions. Reaction engineering leverages the interface where fundamental molecular chemistry meets chemical engineering and technology. Challenges in chemistry can be overcome by the application of new technologies, while engineers may find improved solutions for process development from the latest developments in reaction chemistry. Reaction Chemistry & Engineering is a unique forum for researchers whose interests span the broad areas of chemical engineering and chemical sciences to come together in solving problems of importance to wider society. All papers should be written to be approachable by readers across the engineering and chemical sciences. Papers that consider multiple scales, from the laboratory up to and including plant scale, are particularly encouraged.
![N-[(5,6-Dichloro-1H-benzimidazol-2-yl)methyl]-9-(1-methyl-1H-pyrazol-4-yl)-2-(4-morpholinyl)-9H-purin-6-amine structure N-[(5,6-Dichloro-1H-benzimidazol-2-yl)methyl]-9-(1-methyl-1H-pyrazol-4-yl)-2-(4-morpholinyl)-9H-purin-6-amine structure](https://static.chemtradehub.com/structs/238/2387704-62-1-25f4.webp)



