CO<sub>2</sub> Methanation: Nickel–Alumina Catalyst Prepared by Solid-State Combustion

The development of solvent-free methods for the synthesis of catalysts is one of the main tasks of green chemistry. A nickel–alumina catalyst for CO<sub>2</sub> methanation was synthesized by solid-state combustion method using hexakis-(imidazole) nickel (II) nitrate complex. Using X-ray...

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Autores principales: Olga Netskina, Svetlana Mucha, Janna Veselovskaya, Vasily Bolotov, Oxana Komova, Arkady Ishchenko, Olga Bulavchenko, Igor Prosvirin, Alena Pochtar, Vladimir Rogov
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spelling oai:doaj.org-article:eb7aa654e9da45baa8ace24618bd5c032021-11-25T18:13:35ZCO<sub>2</sub> Methanation: Nickel–Alumina Catalyst Prepared by Solid-State Combustion10.3390/ma142267891996-1944https://doaj.org/article/eb7aa654e9da45baa8ace24618bd5c032021-11-01T00:00:00Zhttps://www.mdpi.com/1996-1944/14/22/6789https://doaj.org/toc/1996-1944The development of solvent-free methods for the synthesis of catalysts is one of the main tasks of green chemistry. A nickel–alumina catalyst for CO<sub>2</sub> methanation was synthesized by solid-state combustion method using hexakis-(imidazole) nickel (II) nitrate complex. Using X-ray Powder Diffraction (XRD), Transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and Hydrogen temperature-programmed reduction (H<sub>2</sub>-TPR), it was shown that the synthesized catalyst is characterized by the localization of easily reduced nickel oxide on alumina surface. This provided low-temperature activation of the catalyst in the reaction mixture containing 4 vol% CO<sub>2</sub>. In addition, the synthesized catalyst had higher activity in low-temperature CO<sub>2</sub> methanation compared to industrial NIAP-07-01 catalyst, which contained almost three times more hard-to-reduce nickel–aluminum spinel. Thus, the proposed approaches to the synthesis and activation of the catalyst make it possible to simplify the catalyst preparation procedure and to abandon the use of solvents, which must be disposed of later on.Olga NetskinaSvetlana MuchaJanna VeselovskayaVasily BolotovOxana KomovaArkady IshchenkoOlga BulavchenkoIgor ProsvirinAlena PochtarVladimir RogovMDPI AGarticleCO<sub>2</sub> methanationnickel–alumina catalystsolid-state combustion methodcatalyst activationTechnologyTElectrical engineering. Electronics. Nuclear engineeringTK1-9971Engineering (General). Civil engineering (General)TA1-2040MicroscopyQH201-278.5Descriptive and experimental mechanicsQC120-168.85ENMaterials, Vol 14, Iss 6789, p 6789 (2021)
institution DOAJ
collection DOAJ
language EN
topic CO<sub>2</sub> methanation
nickel–alumina catalyst
solid-state combustion method
catalyst activation
Technology
T
Electrical engineering. Electronics. Nuclear engineering
TK1-9971
Engineering (General). Civil engineering (General)
TA1-2040
Microscopy
QH201-278.5
Descriptive and experimental mechanics
QC120-168.85
spellingShingle CO<sub>2</sub> methanation
nickel–alumina catalyst
solid-state combustion method
catalyst activation
Technology
T
Electrical engineering. Electronics. Nuclear engineering
TK1-9971
Engineering (General). Civil engineering (General)
TA1-2040
Microscopy
QH201-278.5
Descriptive and experimental mechanics
QC120-168.85
Olga Netskina
Svetlana Mucha
Janna Veselovskaya
Vasily Bolotov
Oxana Komova
Arkady Ishchenko
Olga Bulavchenko
Igor Prosvirin
Alena Pochtar
Vladimir Rogov
CO<sub>2</sub> Methanation: Nickel–Alumina Catalyst Prepared by Solid-State Combustion
description The development of solvent-free methods for the synthesis of catalysts is one of the main tasks of green chemistry. A nickel–alumina catalyst for CO<sub>2</sub> methanation was synthesized by solid-state combustion method using hexakis-(imidazole) nickel (II) nitrate complex. Using X-ray Powder Diffraction (XRD), Transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and Hydrogen temperature-programmed reduction (H<sub>2</sub>-TPR), it was shown that the synthesized catalyst is characterized by the localization of easily reduced nickel oxide on alumina surface. This provided low-temperature activation of the catalyst in the reaction mixture containing 4 vol% CO<sub>2</sub>. In addition, the synthesized catalyst had higher activity in low-temperature CO<sub>2</sub> methanation compared to industrial NIAP-07-01 catalyst, which contained almost three times more hard-to-reduce nickel–aluminum spinel. Thus, the proposed approaches to the synthesis and activation of the catalyst make it possible to simplify the catalyst preparation procedure and to abandon the use of solvents, which must be disposed of later on.
format article
author Olga Netskina
Svetlana Mucha
Janna Veselovskaya
Vasily Bolotov
Oxana Komova
Arkady Ishchenko
Olga Bulavchenko
Igor Prosvirin
Alena Pochtar
Vladimir Rogov
author_facet Olga Netskina
Svetlana Mucha
Janna Veselovskaya
Vasily Bolotov
Oxana Komova
Arkady Ishchenko
Olga Bulavchenko
Igor Prosvirin
Alena Pochtar
Vladimir Rogov
author_sort Olga Netskina
title CO<sub>2</sub> Methanation: Nickel–Alumina Catalyst Prepared by Solid-State Combustion
title_short CO<sub>2</sub> Methanation: Nickel–Alumina Catalyst Prepared by Solid-State Combustion
title_full CO<sub>2</sub> Methanation: Nickel–Alumina Catalyst Prepared by Solid-State Combustion
title_fullStr CO<sub>2</sub> Methanation: Nickel–Alumina Catalyst Prepared by Solid-State Combustion
title_full_unstemmed CO<sub>2</sub> Methanation: Nickel–Alumina Catalyst Prepared by Solid-State Combustion
title_sort co<sub>2</sub> methanation: nickel–alumina catalyst prepared by solid-state combustion
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/eb7aa654e9da45baa8ace24618bd5c03
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