Fe–Ce–Al Catalysts for Decomposition of Methane to High Purity Hydrogen and High-Value Carbon

Catalytic methane decomposition is a promising technique for COx-free hydrogen production and carbon nanomaterials. In this research, iron-supported catalysts, prepared by successive wetness impregnation, were studied for methane decomposition at 700 °C. The results showed that Fe0 turned out to be the active site and greater metal–support interaction led to the formation of iron aluminate (FeAl2O4), both of which played a role in the catalytic activity performance. The 30Fe/Ce–Al catalyst performed the best catalytic activity in terms of maximum methane conversion (76%) and hydrogen production rate (1.04 mol/gMetal/s/surface area). The observation also suggested that the 10Fe/Ce–Al catalyst significantly deactivated due to metal particle agglomeration, as evidenced by negligible weight loss in thermogravimetric analysis. In contrast, the 20Fe/Ce–Al and 30Fe/Ce–Al catalysts were deactivated from both agglomeration and carbon deposition. The surface morphology analysis of the spent catalyst indicated that the deposited carbon was multiwalled carbon nanotubes that followed the base-growth mechanism.

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Publication Details

Journal
Industrial & Engineering Chemistry Research
Published
2024-10-28
DOI
https://doi.org/10.1021/acs.iecr.4c02856
Citations
8
Primary Topic
Catalysts for Methane Reforming
Type
article
Field-Weighted Citation Impact
0.86

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article

Fe–Ce–Al Catalysts for Decomposition of Methane to High Purity Hydrogen and High-Value Carbon

Wasim Ullah Khan, Dwi Hantoko, Ahmed Al Shoaibi, C. Srinivasakannan et al.
8 citations
Industrial & Engineering Chemistry Research
Catalysts for Methane Reforming
0.86
article

Fe–Ce–Al Catalysts for Decomposition of Methane to High Purity Hydrogen and High-Value Carbon

Wasim Ullah Khan, Dwi Hantoko, Ahmed Al Shoaibi, C. Srinivasakannan, Aprizon Putra, Mohammad M. Hossain
article en
8 citations

Abstract

Catalytic methane decomposition is a promising technique for COx-free hydrogen production and carbon nanomaterials. In this research, iron-supported catalysts, prepared by successive wetness impregnation, were studied for methane decomposition at 700 °C. The results showed that Fe0 turned out to be the active site and greater metal–support interaction led to the formation of iron aluminate (FeAl2O4), both of which played a role in the catalytic activity performance. The 30Fe/Ce–Al catalyst performed the best catalytic activity in terms of maximum methane conversion (76%) and hydrogen production rate (1.04 mol/gMetal/s/surface area). The observation also suggested that the 10Fe/Ce–Al catalyst significantly deactivated due to metal particle agglomeration, as evidenced by negligible weight loss in thermogravimetric analysis. In contrast, the 20Fe/Ce–Al and 30Fe/Ce–Al catalysts were deactivated from both agglomeration and carbon deposition. The surface morphology analysis of the spent catalyst indicated that the deposited carbon was multiwalled carbon nanotubes that followed the base-growth mechanism.

Industrial & Engineering Chemistry ResearchVol. 63(44)
King Fahd University of Petroleum and Minerals (SA), Khalifa University of Science and Technology (AE)
King Fahd University of Petroleum and Minerals
Openalex Percentile: Top 31%
Catalysts for Methane Reforming
0.86
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