A comparative study of dry reforming of methane over nickel catalysts supported on perovskite-type LaAlO3 and commercial a-Al2O3
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRN |
Texto Completo: | https://repositorio.ufrn.br/handle/123456789/45283 |
Resumo: | A systematic and comparative study was made to determine the influence of perovskite-type LaAlO3 and commercial a-Al2O3 on the performance of nickel-based catalysts in dry reforming of methane (DRM). The perovskite-type LaAlO3 was selected due to its characteristics of solid state semiconductor with oxygen vacancies and high structural stability. The catalysts were characterized by X-ray diffraction (XRD), X-ray fluorescence spectroscopy (XRF), N2 adsorption-desorption, temperature programmed reduction (TPR-H2), thermogravimetric analysis (TGA), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The catalyst performance was evaluated based on activity tests (600e800 C) and short- and long-term stability (10 and 20 h) at 700 C at a GHSV (Gas Hourly Space Velocity) of 18 and 72 L g1 h1. The TPR-H2 profiles indicate that the oxygen vacancies on the perovskite surface exerted a strong effect on the reduction temperature and reducibility of the NiO nanoparticles, resulting in weak Ni0/support interaction. The results of the tests after 10 h under GHSV of 18 L g1 h1 indicate that the Ni/LaAlO3 catalyst is 7.8 and 11.5% more stable than Ni/a-Al2O3 in the conversions of CH4 and CO2, respectively. The higher stability and activity of Ni/LaAlO3 is directly ascribed to the presence of NiO (3.38 wt%) after activation, which promoted the formation of carbon nanotubes (CNT) and increased the dispersion of the metallic phase. Even under severe conditions of activation and reaction (high GHSV), as in the long-term test, the Ni/LaAlO3 catalyst showed a 37.2% higher H2 yield than the Ni/a-Al2O3. Analyses by TEM indicate that the Ni/a-Al2O3 catalyst exhibited deactivation problems associated with sintering effects. Thus, the presence of structural defects and surfaces rich in oxygen vacancies makes LaAlO3 perovskite a potential support for application in methane catalytic reforming processes |
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Melo, Marcus Antônio de FreitasFigueredo, Gilvan Pereira deMedeiros, Rodolfo Luiz Bezerra de AraújoMacedo, Heloísa Pimenta deOliveira, Ângelo Anderson Silva deBraga, Renata MartinsMercury, José Manuel RivasMelo, Dulce Maria de Araújo2021-12-08T16:51:51Z2021-12-08T16:51:51Z2018-06-14FIGUEREDO, G. P.; MEDEIROS, R. L.B.A.; MACEDO, H. P.; OLIVEIRA, Â. A.S.; BRAGA, R. M.; MERCURY, J. M.R.; MELO, M. A. F.; MELO, D. M. A.. A comparative study of dry reforming of methane over nickel catalysts supported on perovskite-type LaAlO 3 and commercial α-Al 2 O 3. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, v. 43, p. 11022-11037, 2018. Disponível em: https://www.sciencedirect.com/science/article/abs/pii/S0360319918314484. Acesso em: 06 out. 2021. https://doi.org/10.1016/j.ijhydene.2018.04.224.0360-3199https://repositorio.ufrn.br/handle/123456789/4528310.1016/j.ijhydene.2018.04.224ElsevierHydrogenCarbon nanotubesMicrowave synthesisLaAlO3NiDry reforming of methaneA comparative study of dry reforming of methane over nickel catalysts supported on perovskite-type LaAlO3 and commercial a-Al2O3info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleA systematic and comparative study was made to determine the influence of perovskite-type LaAlO3 and commercial a-Al2O3 on the performance of nickel-based catalysts in dry reforming of methane (DRM). The perovskite-type LaAlO3 was selected due to its characteristics of solid state semiconductor with oxygen vacancies and high structural stability. The catalysts were characterized by X-ray diffraction (XRD), X-ray fluorescence spectroscopy (XRF), N2 adsorption-desorption, temperature programmed reduction (TPR-H2), thermogravimetric analysis (TGA), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The catalyst performance was evaluated based on activity tests (600e800 C) and short- and long-term stability (10 and 20 h) at 700 C at a GHSV (Gas Hourly Space Velocity) of 18 and 72 L g1 h1. The TPR-H2 profiles indicate that the oxygen vacancies on the perovskite surface exerted a strong effect on the reduction temperature and reducibility of the NiO nanoparticles, resulting in weak Ni0/support interaction. The results of the tests after 10 h under GHSV of 18 L g1 h1 indicate that the Ni/LaAlO3 catalyst is 7.8 and 11.5% more stable than Ni/a-Al2O3 in the conversions of CH4 and CO2, respectively. The higher stability and activity of Ni/LaAlO3 is directly ascribed to the presence of NiO (3.38 wt%) after activation, which promoted the formation of carbon nanotubes (CNT) and increased the dispersion of the metallic phase. Even under severe conditions of activation and reaction (high GHSV), as in the long-term test, the Ni/LaAlO3 catalyst showed a 37.2% higher H2 yield than the Ni/a-Al2O3. Analyses by TEM indicate that the Ni/a-Al2O3 catalyst exhibited deactivation problems associated with sintering effects. Thus, the presence of structural defects and surfaces rich in oxygen vacancies makes LaAlO3 perovskite a potential support for application in methane catalytic reforming processesengreponame:Repositório Institucional da UFRNinstname:Universidade Federal do Rio Grande do Norte (UFRN)instacron:UFRNinfo:eu-repo/semantics/openAccessCC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-8914https://repositorio.ufrn.br/bitstream/123456789/45283/2/license_rdf4d2950bda3d176f570a9f8b328dfbbefMD52LICENSElicense.txtlicense.txttext/plain; charset=utf-81484https://repositorio.ufrn.br/bitstream/123456789/45283/3/license.txte9597aa2854d128fd968be5edc8a28d9MD53123456789/452832023-02-07 17:49:19.198oai:https://repositorio.ufrn.br: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Repositório de PublicaçõesPUBhttp://repositorio.ufrn.br/oai/opendoar:2023-02-07T20:49:19Repositório Institucional da UFRN - Universidade Federal do Rio Grande do Norte (UFRN)false |
dc.title.pt_BR.fl_str_mv |
A comparative study of dry reforming of methane over nickel catalysts supported on perovskite-type LaAlO3 and commercial a-Al2O3 |
title |
A comparative study of dry reforming of methane over nickel catalysts supported on perovskite-type LaAlO3 and commercial a-Al2O3 |
spellingShingle |
A comparative study of dry reforming of methane over nickel catalysts supported on perovskite-type LaAlO3 and commercial a-Al2O3 Melo, Marcus Antônio de Freitas Hydrogen Carbon nanotubes Microwave synthesis LaAlO3 Ni Dry reforming of methane |
title_short |
A comparative study of dry reforming of methane over nickel catalysts supported on perovskite-type LaAlO3 and commercial a-Al2O3 |
title_full |
A comparative study of dry reforming of methane over nickel catalysts supported on perovskite-type LaAlO3 and commercial a-Al2O3 |
title_fullStr |
A comparative study of dry reforming of methane over nickel catalysts supported on perovskite-type LaAlO3 and commercial a-Al2O3 |
title_full_unstemmed |
A comparative study of dry reforming of methane over nickel catalysts supported on perovskite-type LaAlO3 and commercial a-Al2O3 |
title_sort |
A comparative study of dry reforming of methane over nickel catalysts supported on perovskite-type LaAlO3 and commercial a-Al2O3 |
author |
Melo, Marcus Antônio de Freitas |
author_facet |
Melo, Marcus Antônio de Freitas Figueredo, Gilvan Pereira de Medeiros, Rodolfo Luiz Bezerra de Araújo Macedo, Heloísa Pimenta de Oliveira, Ângelo Anderson Silva de Braga, Renata Martins Mercury, José Manuel Rivas Melo, Dulce Maria de Araújo |
author_role |
author |
author2 |
Figueredo, Gilvan Pereira de Medeiros, Rodolfo Luiz Bezerra de Araújo Macedo, Heloísa Pimenta de Oliveira, Ângelo Anderson Silva de Braga, Renata Martins Mercury, José Manuel Rivas Melo, Dulce Maria de Araújo |
author2_role |
author author author author author author author |
dc.contributor.author.fl_str_mv |
Melo, Marcus Antônio de Freitas Figueredo, Gilvan Pereira de Medeiros, Rodolfo Luiz Bezerra de Araújo Macedo, Heloísa Pimenta de Oliveira, Ângelo Anderson Silva de Braga, Renata Martins Mercury, José Manuel Rivas Melo, Dulce Maria de Araújo |
dc.subject.por.fl_str_mv |
Hydrogen Carbon nanotubes Microwave synthesis LaAlO3 Ni Dry reforming of methane |
topic |
Hydrogen Carbon nanotubes Microwave synthesis LaAlO3 Ni Dry reforming of methane |
description |
A systematic and comparative study was made to determine the influence of perovskite-type LaAlO3 and commercial a-Al2O3 on the performance of nickel-based catalysts in dry reforming of methane (DRM). The perovskite-type LaAlO3 was selected due to its characteristics of solid state semiconductor with oxygen vacancies and high structural stability. The catalysts were characterized by X-ray diffraction (XRD), X-ray fluorescence spectroscopy (XRF), N2 adsorption-desorption, temperature programmed reduction (TPR-H2), thermogravimetric analysis (TGA), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The catalyst performance was evaluated based on activity tests (600e800 C) and short- and long-term stability (10 and 20 h) at 700 C at a GHSV (Gas Hourly Space Velocity) of 18 and 72 L g1 h1. The TPR-H2 profiles indicate that the oxygen vacancies on the perovskite surface exerted a strong effect on the reduction temperature and reducibility of the NiO nanoparticles, resulting in weak Ni0/support interaction. The results of the tests after 10 h under GHSV of 18 L g1 h1 indicate that the Ni/LaAlO3 catalyst is 7.8 and 11.5% more stable than Ni/a-Al2O3 in the conversions of CH4 and CO2, respectively. The higher stability and activity of Ni/LaAlO3 is directly ascribed to the presence of NiO (3.38 wt%) after activation, which promoted the formation of carbon nanotubes (CNT) and increased the dispersion of the metallic phase. Even under severe conditions of activation and reaction (high GHSV), as in the long-term test, the Ni/LaAlO3 catalyst showed a 37.2% higher H2 yield than the Ni/a-Al2O3. Analyses by TEM indicate that the Ni/a-Al2O3 catalyst exhibited deactivation problems associated with sintering effects. Thus, the presence of structural defects and surfaces rich in oxygen vacancies makes LaAlO3 perovskite a potential support for application in methane catalytic reforming processes |
publishDate |
2018 |
dc.date.issued.fl_str_mv |
2018-06-14 |
dc.date.accessioned.fl_str_mv |
2021-12-08T16:51:51Z |
dc.date.available.fl_str_mv |
2021-12-08T16:51:51Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
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article |
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publishedVersion |
dc.identifier.citation.fl_str_mv |
FIGUEREDO, G. P.; MEDEIROS, R. L.B.A.; MACEDO, H. P.; OLIVEIRA, Â. A.S.; BRAGA, R. M.; MERCURY, J. M.R.; MELO, M. A. F.; MELO, D. M. A.. A comparative study of dry reforming of methane over nickel catalysts supported on perovskite-type LaAlO 3 and commercial α-Al 2 O 3. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, v. 43, p. 11022-11037, 2018. Disponível em: https://www.sciencedirect.com/science/article/abs/pii/S0360319918314484. Acesso em: 06 out. 2021. https://doi.org/10.1016/j.ijhydene.2018.04.224. |
dc.identifier.uri.fl_str_mv |
https://repositorio.ufrn.br/handle/123456789/45283 |
dc.identifier.issn.none.fl_str_mv |
0360-3199 |
dc.identifier.doi.none.fl_str_mv |
10.1016/j.ijhydene.2018.04.224 |
identifier_str_mv |
FIGUEREDO, G. P.; MEDEIROS, R. L.B.A.; MACEDO, H. P.; OLIVEIRA, Â. A.S.; BRAGA, R. M.; MERCURY, J. M.R.; MELO, M. A. F.; MELO, D. M. A.. A comparative study of dry reforming of methane over nickel catalysts supported on perovskite-type LaAlO 3 and commercial α-Al 2 O 3. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, v. 43, p. 11022-11037, 2018. Disponível em: https://www.sciencedirect.com/science/article/abs/pii/S0360319918314484. Acesso em: 06 out. 2021. https://doi.org/10.1016/j.ijhydene.2018.04.224. 0360-3199 10.1016/j.ijhydene.2018.04.224 |
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