Catalytic Reforming of Light Hydrocarbons

A special issue of Catalysts (ISSN 2073-4344). This special issue belongs to the section "Catalysis for Sustainable Energy".

Deadline for manuscript submissions: closed (30 September 2023) | Viewed by 8950

Special Issue Editor


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Guest Editor
Chemical Engineering Department, College of Engineering, King Saud University, P.O. Box 800, Riyadh 11421, Saudi Arabia
Interests: catalysis; dry reforming

Special Issue Information

Dear Colleagues,

Reforming has emerged as an advanced process due to its great potential as a green and eco-friendly process for the treatment and mitigation of greenhouse gases and the production of value-added compounds. In this context, the reforming of light hydrocarbons such as methane has been shown to be a prominent method for the generation of useful products such as synthesis gas. Since ancient times, the production of syngas has been known as the most efficient for obtaining the products of the Fischer–Tropsch processand other precious compounds. At present, it has been widely studied in academic research and used in a variety of advanced catalytic applications, including the dry reforming, steam reforming, and oxidative reforming of light hydrocarbons, as well as CO2 reduction.

This Special Issue, Catalytic Reforming of Light Hydrocarbons, covers the design, preparation, characterization, and catalytic performance of light hydrocarbon reforming using a variety of heterogeneous catalysts. We invite authors to contribute original research and review articles with special emphasis on CH4, C2H4, and CO2 reduction and environmental remediation.

Prof. Dr. Ahmed Sadeq A. Al-Fatesh
Guest Editor

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Keywords

  • methane reforming
  • methane decomposition
  • heterogeneous catalysis
  • metal oxides
  • supports of various structures
  • stability study
  • reduction of global warming
  • investigation of catalyst deactivation
  • formation of value-added carbon

Published Papers (5 papers)

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Research

12 pages, 2785 KiB  
Article
Fe-Promoted Alumina-Supported Ni Catalyst Stabilized by Zirconia for Methane Dry Reforming
by Anis H. Fakeeha, Yousef A. Al-Baqmaa, Ahmed A. Ibrahim, Fahad S. Almubaddel, Mohammed F. Alotibi, Abdulaziz Bentalib, Ahmed E. Abasaeed, Ateyah A. Al-Zahrani, Yahya Ahmed Mohammed and Ahmed S. Al-Fatesh
Catalysts 2023, 13(5), 806; https://0-doi-org.brum.beds.ac.uk/10.3390/catal13050806 - 27 Apr 2023
Cited by 1 | Viewed by 1189
Abstract
The dry reforming of methane is a highly popular procedure since it can transform two of the most abundant greenhouse gases, methane and carbon dioxide, into useful syngases that can be further processed into valuable chemicals. To successfully achieve this conversion for the [...] Read more.
The dry reforming of methane is a highly popular procedure since it can transform two of the most abundant greenhouse gases, methane and carbon dioxide, into useful syngases that can be further processed into valuable chemicals. To successfully achieve this conversion for the effective production of syngas, an optimal catalyst with advantageous physicochemical features must be developed. In this study, a variety of Ni-based catalysts supported by zirconia alumina (5Ni-10Zr + Al) were prepared by using the impregnation approach. Different loadings of Fe promoter were used, and the performances of the resulting catalysts in terms of activity and stability were investigated. The catalyst used in this study had an active metal component made of 5% Ni and x% Fe supported on 10ZrO2 + Al2O3, where x = (1, 2, 3, and 4). The physicochemical characteristics of both freshly calcined and used catalysts were studied using a range of characterization techniques, such as: N2 adsorption–desorption isotherms, XRD, H2-TPR, Raman spectroscopy, TGA, and TEM. An investigation of the effects of the Fe promoter on the catalytic activity of the catalyst (5Ni + xFe-10Zr + Al) was conducted. Amongst the studied catalysts, the 5Ni + 3Fe-10Zr + Al catalyst showed the best catalytic activity with CH4 and CO2 conversions of 87% and 90%, respectively, and had an H2/CO ratio of 0.98. Full article
(This article belongs to the Special Issue Catalytic Reforming of Light Hydrocarbons)
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15 pages, 2637 KiB  
Article
Carbon Dioxide Valorization into Methane Using Samarium Oxide-Supported Monometallic and Bimetallic Catalysts
by Radwa A. El-Salamony, Ahmed S. Al-Fatesh, Kenit Acharya, Abdulaziz A. M. Abahussain, Abdulaziz Bagabas, Nadavala Siva Kumar, Ahmed A. Ibrahim, Wasim Ullah Khan and Rawesh Kumar
Catalysts 2023, 13(1), 113; https://0-doi-org.brum.beds.ac.uk/10.3390/catal13010113 - 04 Jan 2023
Cited by 6 | Viewed by 1581
Abstract
Samarium oxide (Sm2O3) is a versatile surface for CO2 and H2 interaction and conversion. Samarium oxide-supported Ni, samarium oxide-supported Co-Ni, and samarium oxide-supported Ru-Ni catalysts were tested for CO2 methanation and were characterized by X-ray diffraction, [...] Read more.
Samarium oxide (Sm2O3) is a versatile surface for CO2 and H2 interaction and conversion. Samarium oxide-supported Ni, samarium oxide-supported Co-Ni, and samarium oxide-supported Ru-Ni catalysts were tested for CO2 methanation and were characterized by X-ray diffraction, nitrogen physisorption, infrared spectroscopy, H2-temperature programmed reduction, and X-ray photoelectron spectroscopy. Limited H2 dissociation and widely available surface carbonate and formate species over 20 wt.% Ni, dispersed over Sm2O3, resulted in ~98% CH4 selectivity. The low selectivity for CO could be due to the reforming reaction between CH4 (methanation product) and CO2. Co-impregnation of cobalt with nickel over Sm2O3 had high surface adsorbed oxygen and higher CO selectivity. On the other hand, co-impregnation of ruthenium and nickel over Sm2O3 led to more than one catalytic active site, carbonate species, lack of formate species, and 94% CH4 selectivity. It indicated the following route of CH4 synthesis over Ru-Ni/Sm2O3; carbonate → unstable formate → CO → CH4. Full article
(This article belongs to the Special Issue Catalytic Reforming of Light Hydrocarbons)
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14 pages, 2603 KiB  
Article
Effect of Modified Alumina Support on the Performance of Ni-Based Catalysts for CO2 Reforming of Methane
by Salwa Bader Alreshaidan, Ahmed A. Ibrahim, Anis H. Fakeeha, Abdulaziz M. Almutlaq, Fekri Abdulraqeb Ahmed Ali and Ahmed S. Al-Fatesh
Catalysts 2022, 12(9), 1066; https://0-doi-org.brum.beds.ac.uk/10.3390/catal12091066 - 18 Sep 2022
Cited by 11 | Viewed by 1957
Abstract
The CO2 reforming of methane to syngas was examined over five different supported catalysts. In this study, 5% Ni was used as the active metal part of the catalyst. To better comprehend the impact of the supports on the catalytic properties, 5% [...] Read more.
The CO2 reforming of methane to syngas was examined over five different supported catalysts. In this study, 5% Ni was used as the active metal part of the catalyst. To better comprehend the impact of the supports on the catalytic properties, 5% Ni-based catalysts were characterized using nitrogen adsorption–desorption isotherms, XRD, H2-TPR, CO2-TPD, TGA, TPO, FTIR, and Raman. The results showed that the catalyst support with the highest surface area provided the best catalytic activity. The acquired CH4 and CO2 conversions at 700 °C were 58.2% and 67.6%, respectively, with a hydrogen/carbon ratio of 0.85. The TGA investigation of the high-surface-area sample produced a minimum carbon deposition of 11.2 wt.%, and in the CO2-TPD investigation, the high-surface-area sample exhibited the absence of a peak in the strong-basic-sites zone. The formation of NiAl2O4 spinel, moderate basicity, and the high surface area explained the outperformance of the high-surface-area catalyst sample. Full article
(This article belongs to the Special Issue Catalytic Reforming of Light Hydrocarbons)
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14 pages, 5072 KiB  
Article
Lanthanum–Cerium-Modified Nickel Catalysts for Dry Reforming of Methane
by Mahmud S. Lanre, Ahmed E. Abasaeed, Anis H. Fakeeha, Ahmed A. Ibrahim, Abdulrahman S. Al-Awadi, Abdulrahman bin Jumah, Fahad S. Al-Mubaddel and Ahmed S. Al-Fatesh
Catalysts 2022, 12(7), 715; https://0-doi-org.brum.beds.ac.uk/10.3390/catal12070715 - 29 Jun 2022
Cited by 9 | Viewed by 1613
Abstract
The catalyst MNi0.9Zr0.1O3 (M = La, Ce, and Cs) was prepared using the sol–gel preparation technique investigated for the dry reforming of methane reaction to examine activity, stability, and H2/CO ratio. The lanthanum in the catalyst [...] Read more.
The catalyst MNi0.9Zr0.1O3 (M = La, Ce, and Cs) was prepared using the sol–gel preparation technique investigated for the dry reforming of methane reaction to examine activity, stability, and H2/CO ratio. The lanthanum in the catalyst LaNi0.9Zr0.1O3 was partially substituted for cerium and zirconium for yttrium to give La0.6Ce0.4Ni0.9Zr0.1−xYxO3 (x = 0.05, 0.07, and 0.09). The La0.6Ce0.4Ni0.9Zr0.1−xYxO3 catalyst’s activity increases with an increase in yttrium loading. The activities of the yttrium-modified catalysts La0.6Ce0.4Ni0.9Zr0.03Y0.07O3 and La0.6Ce0.4Ni0.9Zr0.01Y0.09O3 are higher than the unmodified La0.6Ce0.4Ni0.9Zr0.1O3 catalyst, the latter having methane and carbon dioxide conversion values of 84% and 87%, respectively, and the former with methane and carbon dioxide conversion values of 86% and 90% for La0.6Ce0.4Ni0.9Zr0.03Y0.07O3 and 89% and 91% for La0.6Ce0.4Ni0.9Zr0.01Y0.09O3, respectively. The BET analysis depicted a low surface area of samples ranging from 2 to 9 m2/g. The XRD peaks confirmed the formation of a monoclinic phase of zirconium. The TPR showed that apparent reduction peaks occurred in moderate temperature regions. The TGA curve showed weight loss steps in the range 773 K–973 K, with CsNi0.9Zr0.1O3 carbon deposition being the most severe. The coke deposit on La0.6Ce0.4Ni0.9Zr0.1O3 after 7 h time on stream (TOS) was the lowest, with 20% weight loss. The amount of weight loss increases with a decrease in zirconium loading. Full article
(This article belongs to the Special Issue Catalytic Reforming of Light Hydrocarbons)
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17 pages, 6044 KiB  
Article
Optimizing MgO Content for Boosting γ-Al2O3-Supported Ni Catalyst in Dry Reforming of Methane
by Abdulaziz Bagabas, Ahmed Sadeq Al-Fatesh, Samsudeen Olajide Kasim, Rasheed Arasheed, Ahmed Aidid Ibrahim, Rawan Ashamari, Khalid Anojaidi, Anis Hamza Fakeeha, Jehad K. Abu-Dahrieh and Ahmed Elhag Abasaeed
Catalysts 2021, 11(10), 1233; https://0-doi-org.brum.beds.ac.uk/10.3390/catal11101233 - 13 Oct 2021
Cited by 8 | Viewed by 1811
Abstract
The dry reforming of methane (DRM) process has attracted research interest because of its ability to mitigate the detrimental impacts of greenhouse gases such as methane (CH4) and carbon dioxide (CO2) and produce alcohols and clean fuel. In view [...] Read more.
The dry reforming of methane (DRM) process has attracted research interest because of its ability to mitigate the detrimental impacts of greenhouse gases such as methane (CH4) and carbon dioxide (CO2) and produce alcohols and clean fuel. In view of this importance of DRM, we disclosed the efficiency of a new nickel-based catalyst, which was promoted with magnesia (MgO) and supported over gamma-alumina (γ-Al2O3) doped with silica (SiO2), toward DRM. The synthesized catalysts were characterized by H2 temperature-programmed reduction (H2-TPR), X-ray diffraction (XRD), X-ray Photoelectron Spectroscopy (XPS), Thermogravimetric analysis (TGA), and Transmission electron microscopy (TEM) techniques. The effect of MgO weight percent loading (0.0, 1.0, 2.0, and 3.0 wt. %) was examined because the catalytic performance was found to be a function of this parameter. An optimum loading of 2.0 wt. % of MgO was obtained, where the conversion of CH4 and CO2 at 800 °C were 86% and 91%, respectively, while the syngas (H2/CO) ratios relied on temperature and were in the range of 0.85 to 0.95. The TGA measurement of the best catalyst, which was operated over a 15-h reaction time, displayed negligible weight loss (<9.0 wt. %) due to carbon deposition, indicating the good resistance of our catalyst system to the deposition of carbon owing to the dopant and the modifier. TEM images showed the presence of multiwalled carbon nanotubes, confirming the TGA. Full article
(This article belongs to the Special Issue Catalytic Reforming of Light Hydrocarbons)
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