CO2 reactivity with Mg2NiH4 synthesized by: In situ monitoring of mechanical milling
- Autores
- Grasso, María Laura; Puszkiel, Julián Atilio; Gennari, Fabiana Cristina; Santoru, Antonio; Dornheim, Martin; Pistidda, Claudio
- Año de publicación
- 2020
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- CO2 capture and conversion are a key research field for the transition towards an economy only based on renewable energy sources. In this regard, hydride materials are a potential option for CO2 methanation since they can provide hydrogen and act as a catalytic species. In this work, Mg2NiH4 complex hydride is synthesized by in situ monitoring of mechanical milling under a hydrogen atmosphere from a 2MgH2:Ni stoichiometric mixture. Temperature and pressure evolution is monitored, and the material is characterized, during milling in situ, thus providing a good insight into the synthesis process. The cubic polymorph of Mg2NiH4 (S.G. Fm3m) starts to be formed in the early beginning of the mechanical treatment due to the mechanical stress induced by the milling process. Then, after 25 hours of milling, Mg2NiH4 with a monoclinic (S.G. C12/c1) structure appears. The formation of the monoclinic polymorph is most likely related to the stress release that follows the continuous refinement of the material's microstructure. At the end of the milling process, after 60 hours, the as-milled material is composed of 90.8 wt% cubic Mg2NiH4, 5.7 wt% monoclinic Mg2NiH4, and 3.5 wt% remnant Ni. The as-milled Mg2NiH4 shows high reactivity for CO2 conversion into CH4. Under static conditions at 400 °C for 5 hours, the interactions between as-milled Mg2NiH4 and CO2 result in total CO2 consumption and in the formation of the catalytic system Ni-MgNi2-Mg2Ni/MgO. Experimental evidence and thermodynamic equilibrium calculations suggest that the global methanation mechanism takes place through the adsorption of C and the direct solid gasification towards CH4 formation.
Fil: Grasso, María Laura. Comisión Nacional de Energía Atómica. Gerencia de Área de Aplicaciones de la Tecnología Nuclear. Gerencia de Investigación Aplicada CAB. Departamento Fisicoquímica de Materiales; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte; Argentina
Fil: Puszkiel, Julián Atilio. Comisión Nacional de Energía Atómica. Gerencia de Área de Aplicaciones de la Tecnología Nuclear. Gerencia de Investigación Aplicada CAB. Departamento Fisicoquímica de Materiales; Argentina. Helmholtz-Zentrum Geesthacht GmbH; Alemania. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte; Argentina
Fil: Gennari, Fabiana Cristina. Comisión Nacional de Energía Atómica. Gerencia de Área de Aplicaciones de la Tecnología Nuclear. Gerencia de Investigación Aplicada CAB. Departamento Fisicoquímica de Materiales; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte; Argentina
Fil: Santoru, Antonio. Helmholtz-Zentrum Geesthacht GmbH; Alemania
Fil: Dornheim, Martin. Helmholtz-Zentrum Geesthacht GmbH; Alemania
Fil: Pistidda, Claudio. Helmholtz-Zentrum Geesthacht GmbH; Alemania - Materia
-
CARBON DIOXIDE
HYDRIDE
CONVERSION
METHANE - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/126642
Ver los metadatos del registro completo
id |
CONICETDig_3d76ef036d8556cf51c98a70f0ed7166 |
---|---|
oai_identifier_str |
oai:ri.conicet.gov.ar:11336/126642 |
network_acronym_str |
CONICETDig |
repository_id_str |
3498 |
network_name_str |
CONICET Digital (CONICET) |
spelling |
CO2 reactivity with Mg2NiH4 synthesized by: In situ monitoring of mechanical millingGrasso, María LauraPuszkiel, Julián AtilioGennari, Fabiana CristinaSantoru, AntonioDornheim, MartinPistidda, ClaudioCARBON DIOXIDEHYDRIDECONVERSIONMETHANEhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1CO2 capture and conversion are a key research field for the transition towards an economy only based on renewable energy sources. In this regard, hydride materials are a potential option for CO2 methanation since they can provide hydrogen and act as a catalytic species. In this work, Mg2NiH4 complex hydride is synthesized by in situ monitoring of mechanical milling under a hydrogen atmosphere from a 2MgH2:Ni stoichiometric mixture. Temperature and pressure evolution is monitored, and the material is characterized, during milling in situ, thus providing a good insight into the synthesis process. The cubic polymorph of Mg2NiH4 (S.G. Fm3m) starts to be formed in the early beginning of the mechanical treatment due to the mechanical stress induced by the milling process. Then, after 25 hours of milling, Mg2NiH4 with a monoclinic (S.G. C12/c1) structure appears. The formation of the monoclinic polymorph is most likely related to the stress release that follows the continuous refinement of the material's microstructure. At the end of the milling process, after 60 hours, the as-milled material is composed of 90.8 wt% cubic Mg2NiH4, 5.7 wt% monoclinic Mg2NiH4, and 3.5 wt% remnant Ni. The as-milled Mg2NiH4 shows high reactivity for CO2 conversion into CH4. Under static conditions at 400 °C for 5 hours, the interactions between as-milled Mg2NiH4 and CO2 result in total CO2 consumption and in the formation of the catalytic system Ni-MgNi2-Mg2Ni/MgO. Experimental evidence and thermodynamic equilibrium calculations suggest that the global methanation mechanism takes place through the adsorption of C and the direct solid gasification towards CH4 formation.Fil: Grasso, María Laura. Comisión Nacional de Energía Atómica. Gerencia de Área de Aplicaciones de la Tecnología Nuclear. Gerencia de Investigación Aplicada CAB. Departamento Fisicoquímica de Materiales; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte; ArgentinaFil: Puszkiel, Julián Atilio. Comisión Nacional de Energía Atómica. Gerencia de Área de Aplicaciones de la Tecnología Nuclear. Gerencia de Investigación Aplicada CAB. Departamento Fisicoquímica de Materiales; Argentina. Helmholtz-Zentrum Geesthacht GmbH; Alemania. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte; ArgentinaFil: Gennari, Fabiana Cristina. Comisión Nacional de Energía Atómica. Gerencia de Área de Aplicaciones de la Tecnología Nuclear. Gerencia de Investigación Aplicada CAB. Departamento Fisicoquímica de Materiales; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte; ArgentinaFil: Santoru, Antonio. Helmholtz-Zentrum Geesthacht GmbH; AlemaniaFil: Dornheim, Martin. Helmholtz-Zentrum Geesthacht GmbH; AlemaniaFil: Pistidda, Claudio. Helmholtz-Zentrum Geesthacht GmbH; AlemaniaRoyal Society of Chemistry2020-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/126642Grasso, María Laura; Puszkiel, Julián Atilio; Gennari, Fabiana Cristina; Santoru, Antonio; Dornheim, Martin; et al.; CO2 reactivity with Mg2NiH4 synthesized by: In situ monitoring of mechanical milling; Royal Society of Chemistry; Physical Chemistry Chemical Physics; 22; 4; 1-2020; 1944-19521463-90761463-9084CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1039/c9cp05697ainfo:eu-repo/semantics/altIdentifier/url/https://pubs.rsc.org/en/content/articlelanding/2020/cp/c9cp05697a#!divAbstractinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-15T14:26:47Zoai:ri.conicet.gov.ar:11336/126642instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-15 14:26:47.449CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
CO2 reactivity with Mg2NiH4 synthesized by: In situ monitoring of mechanical milling |
title |
CO2 reactivity with Mg2NiH4 synthesized by: In situ monitoring of mechanical milling |
spellingShingle |
CO2 reactivity with Mg2NiH4 synthesized by: In situ monitoring of mechanical milling Grasso, María Laura CARBON DIOXIDE HYDRIDE CONVERSION METHANE |
title_short |
CO2 reactivity with Mg2NiH4 synthesized by: In situ monitoring of mechanical milling |
title_full |
CO2 reactivity with Mg2NiH4 synthesized by: In situ monitoring of mechanical milling |
title_fullStr |
CO2 reactivity with Mg2NiH4 synthesized by: In situ monitoring of mechanical milling |
title_full_unstemmed |
CO2 reactivity with Mg2NiH4 synthesized by: In situ monitoring of mechanical milling |
title_sort |
CO2 reactivity with Mg2NiH4 synthesized by: In situ monitoring of mechanical milling |
dc.creator.none.fl_str_mv |
Grasso, María Laura Puszkiel, Julián Atilio Gennari, Fabiana Cristina Santoru, Antonio Dornheim, Martin Pistidda, Claudio |
author |
Grasso, María Laura |
author_facet |
Grasso, María Laura Puszkiel, Julián Atilio Gennari, Fabiana Cristina Santoru, Antonio Dornheim, Martin Pistidda, Claudio |
author_role |
author |
author2 |
Puszkiel, Julián Atilio Gennari, Fabiana Cristina Santoru, Antonio Dornheim, Martin Pistidda, Claudio |
author2_role |
author author author author author |
dc.subject.none.fl_str_mv |
CARBON DIOXIDE HYDRIDE CONVERSION METHANE |
topic |
CARBON DIOXIDE HYDRIDE CONVERSION METHANE |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
CO2 capture and conversion are a key research field for the transition towards an economy only based on renewable energy sources. In this regard, hydride materials are a potential option for CO2 methanation since they can provide hydrogen and act as a catalytic species. In this work, Mg2NiH4 complex hydride is synthesized by in situ monitoring of mechanical milling under a hydrogen atmosphere from a 2MgH2:Ni stoichiometric mixture. Temperature and pressure evolution is monitored, and the material is characterized, during milling in situ, thus providing a good insight into the synthesis process. The cubic polymorph of Mg2NiH4 (S.G. Fm3m) starts to be formed in the early beginning of the mechanical treatment due to the mechanical stress induced by the milling process. Then, after 25 hours of milling, Mg2NiH4 with a monoclinic (S.G. C12/c1) structure appears. The formation of the monoclinic polymorph is most likely related to the stress release that follows the continuous refinement of the material's microstructure. At the end of the milling process, after 60 hours, the as-milled material is composed of 90.8 wt% cubic Mg2NiH4, 5.7 wt% monoclinic Mg2NiH4, and 3.5 wt% remnant Ni. The as-milled Mg2NiH4 shows high reactivity for CO2 conversion into CH4. Under static conditions at 400 °C for 5 hours, the interactions between as-milled Mg2NiH4 and CO2 result in total CO2 consumption and in the formation of the catalytic system Ni-MgNi2-Mg2Ni/MgO. Experimental evidence and thermodynamic equilibrium calculations suggest that the global methanation mechanism takes place through the adsorption of C and the direct solid gasification towards CH4 formation. Fil: Grasso, María Laura. Comisión Nacional de Energía Atómica. Gerencia de Área de Aplicaciones de la Tecnología Nuclear. Gerencia de Investigación Aplicada CAB. Departamento Fisicoquímica de Materiales; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte; Argentina Fil: Puszkiel, Julián Atilio. Comisión Nacional de Energía Atómica. Gerencia de Área de Aplicaciones de la Tecnología Nuclear. Gerencia de Investigación Aplicada CAB. Departamento Fisicoquímica de Materiales; Argentina. Helmholtz-Zentrum Geesthacht GmbH; Alemania. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte; Argentina Fil: Gennari, Fabiana Cristina. Comisión Nacional de Energía Atómica. Gerencia de Área de Aplicaciones de la Tecnología Nuclear. Gerencia de Investigación Aplicada CAB. Departamento Fisicoquímica de Materiales; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte; Argentina Fil: Santoru, Antonio. Helmholtz-Zentrum Geesthacht GmbH; Alemania Fil: Dornheim, Martin. Helmholtz-Zentrum Geesthacht GmbH; Alemania Fil: Pistidda, Claudio. Helmholtz-Zentrum Geesthacht GmbH; Alemania |
description |
CO2 capture and conversion are a key research field for the transition towards an economy only based on renewable energy sources. In this regard, hydride materials are a potential option for CO2 methanation since they can provide hydrogen and act as a catalytic species. In this work, Mg2NiH4 complex hydride is synthesized by in situ monitoring of mechanical milling under a hydrogen atmosphere from a 2MgH2:Ni stoichiometric mixture. Temperature and pressure evolution is monitored, and the material is characterized, during milling in situ, thus providing a good insight into the synthesis process. The cubic polymorph of Mg2NiH4 (S.G. Fm3m) starts to be formed in the early beginning of the mechanical treatment due to the mechanical stress induced by the milling process. Then, after 25 hours of milling, Mg2NiH4 with a monoclinic (S.G. C12/c1) structure appears. The formation of the monoclinic polymorph is most likely related to the stress release that follows the continuous refinement of the material's microstructure. At the end of the milling process, after 60 hours, the as-milled material is composed of 90.8 wt% cubic Mg2NiH4, 5.7 wt% monoclinic Mg2NiH4, and 3.5 wt% remnant Ni. The as-milled Mg2NiH4 shows high reactivity for CO2 conversion into CH4. Under static conditions at 400 °C for 5 hours, the interactions between as-milled Mg2NiH4 and CO2 result in total CO2 consumption and in the formation of the catalytic system Ni-MgNi2-Mg2Ni/MgO. Experimental evidence and thermodynamic equilibrium calculations suggest that the global methanation mechanism takes place through the adsorption of C and the direct solid gasification towards CH4 formation. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-01 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/126642 Grasso, María Laura; Puszkiel, Julián Atilio; Gennari, Fabiana Cristina; Santoru, Antonio; Dornheim, Martin; et al.; CO2 reactivity with Mg2NiH4 synthesized by: In situ monitoring of mechanical milling; Royal Society of Chemistry; Physical Chemistry Chemical Physics; 22; 4; 1-2020; 1944-1952 1463-9076 1463-9084 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/126642 |
identifier_str_mv |
Grasso, María Laura; Puszkiel, Julián Atilio; Gennari, Fabiana Cristina; Santoru, Antonio; Dornheim, Martin; et al.; CO2 reactivity with Mg2NiH4 synthesized by: In situ monitoring of mechanical milling; Royal Society of Chemistry; Physical Chemistry Chemical Physics; 22; 4; 1-2020; 1944-1952 1463-9076 1463-9084 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1039/c9cp05697a info:eu-repo/semantics/altIdentifier/url/https://pubs.rsc.org/en/content/articlelanding/2020/cp/c9cp05697a#!divAbstract |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Royal Society of Chemistry |
publisher.none.fl_str_mv |
Royal Society of Chemistry |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
_version_ |
1846082716178579456 |
score |
13.22299 |