Hydrogen absorption and desorption in the Mg-Ag system
- Autores
- Urretavizcaya, Guillermina; Sarmiento Chavez, Ana Carolina; Castro, Facundo
- Año de publicación
- 2014
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- We analyze hydrogen absorption and desorption in Mg and Mg?Ag compounds prepared by mechanical milling. The materials were obtained by processing mixtures of Mg or MgH2 with different proportions of Ag under Ar or H2 atmosphere.We observe that Ag and AgMg destabilize MgH2. In the first case the products of the reaction of Ag and MgH2 are AgMg and H2, in the second case MgH2 reacts with AgMg to give AgMg4 and H2. The first reaction was only observed in the forward direction, whereas the second one was registered in both directions. The impossibility to reverse the first reaction was attributed to poor kinetics and experimental limitations. The reversible destabilization induced by AgMg is low, MgH2 overall dehydriding enthalpy is reduced from 76.5 kJ/mol H2 to 69.1 kJ/mol H2. This last value allowed us to estimate the formation enthalpy of AgMg4 at _59.5 kJ/mol. Besides destabilization, a slight improvement in hydrogen absorption kinetics and a more noticeable enhancement in desorption kinetics has been observed in samples containing Ag as an additive. During thermal desorption, the dehydriding temperature decreases by 20 _C. In isothermal desorption experiments at 325 _C, the characteristic induction period of MgH2 without additive practically disappears, and the time to reach 50% of conversion decreases from 17 min to 5.4 min when silver is present. The changes in desorption kinetics could be attributed to AgMg or the interfaces MgH2/AgMg acting as nucleation sites for Mg.
Fil: Urretavizcaya, Guillermina. Comisión Nacional de Energía Atómica. Gerencia del Área de Energía Nuclear. Instituto Balseiro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Sarmiento Chavez, Ana Carolina. Comisión Nacional de Energía Atómica. Gerencia del Área de Energía Nuclear. Instituto Balseiro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Castro, Facundo. Comisión Nacional de Energía Atómica. Gerencia del Área de Energía Nuclear. Instituto Balseiro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina - Materia
-
Hydrogen Absorbing Materials
Intermetallics
Mechanical Milling
Thermodynamic Destabilization
Reaction Pathway
Kinetics - 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:11336/30867
Ver los metadatos del registro completo
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Hydrogen absorption and desorption in the Mg-Ag systemUrretavizcaya, GuillerminaSarmiento Chavez, Ana CarolinaCastro, FacundoHydrogen Absorbing MaterialsIntermetallicsMechanical MillingThermodynamic DestabilizationReaction PathwayKineticsWe analyze hydrogen absorption and desorption in Mg and Mg?Ag compounds prepared by mechanical milling. The materials were obtained by processing mixtures of Mg or MgH2 with different proportions of Ag under Ar or H2 atmosphere.We observe that Ag and AgMg destabilize MgH2. In the first case the products of the reaction of Ag and MgH2 are AgMg and H2, in the second case MgH2 reacts with AgMg to give AgMg4 and H2. The first reaction was only observed in the forward direction, whereas the second one was registered in both directions. The impossibility to reverse the first reaction was attributed to poor kinetics and experimental limitations. The reversible destabilization induced by AgMg is low, MgH2 overall dehydriding enthalpy is reduced from 76.5 kJ/mol H2 to 69.1 kJ/mol H2. This last value allowed us to estimate the formation enthalpy of AgMg4 at _59.5 kJ/mol. Besides destabilization, a slight improvement in hydrogen absorption kinetics and a more noticeable enhancement in desorption kinetics has been observed in samples containing Ag as an additive. During thermal desorption, the dehydriding temperature decreases by 20 _C. In isothermal desorption experiments at 325 _C, the characteristic induction period of MgH2 without additive practically disappears, and the time to reach 50% of conversion decreases from 17 min to 5.4 min when silver is present. The changes in desorption kinetics could be attributed to AgMg or the interfaces MgH2/AgMg acting as nucleation sites for Mg.Fil: Urretavizcaya, Guillermina. Comisión Nacional de Energía Atómica. Gerencia del Área de Energía Nuclear. Instituto Balseiro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Sarmiento Chavez, Ana Carolina. Comisión Nacional de Energía Atómica. Gerencia del Área de Energía Nuclear. Instituto Balseiro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Castro, Facundo. Comisión Nacional de Energía Atómica. Gerencia del Área de Energía Nuclear. Instituto Balseiro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaElsevier Science Sa2014-05-22info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/30867Castro, Facundo; Sarmiento Chavez, Ana Carolina; Urretavizcaya, Guillermina; Hydrogen absorption and desorption in the Mg-Ag system; Elsevier Science Sa; Journal of Alloys and Compounds; 611; 2014; 22-5-2014; 202-2090925-8388CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0925838814011414?via%3Dihubinfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.jallcom.2014.05.066info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-10T13:09:28Zoai:ri.conicet.gov.ar:11336/30867instacron: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:34982025-09-10 13:09:29.103CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Hydrogen absorption and desorption in the Mg-Ag system |
title |
Hydrogen absorption and desorption in the Mg-Ag system |
spellingShingle |
Hydrogen absorption and desorption in the Mg-Ag system Urretavizcaya, Guillermina Hydrogen Absorbing Materials Intermetallics Mechanical Milling Thermodynamic Destabilization Reaction Pathway Kinetics |
title_short |
Hydrogen absorption and desorption in the Mg-Ag system |
title_full |
Hydrogen absorption and desorption in the Mg-Ag system |
title_fullStr |
Hydrogen absorption and desorption in the Mg-Ag system |
title_full_unstemmed |
Hydrogen absorption and desorption in the Mg-Ag system |
title_sort |
Hydrogen absorption and desorption in the Mg-Ag system |
dc.creator.none.fl_str_mv |
Urretavizcaya, Guillermina Sarmiento Chavez, Ana Carolina Castro, Facundo |
author |
Urretavizcaya, Guillermina |
author_facet |
Urretavizcaya, Guillermina Sarmiento Chavez, Ana Carolina Castro, Facundo |
author_role |
author |
author2 |
Sarmiento Chavez, Ana Carolina Castro, Facundo |
author2_role |
author author |
dc.subject.none.fl_str_mv |
Hydrogen Absorbing Materials Intermetallics Mechanical Milling Thermodynamic Destabilization Reaction Pathway Kinetics |
topic |
Hydrogen Absorbing Materials Intermetallics Mechanical Milling Thermodynamic Destabilization Reaction Pathway Kinetics |
dc.description.none.fl_txt_mv |
We analyze hydrogen absorption and desorption in Mg and Mg?Ag compounds prepared by mechanical milling. The materials were obtained by processing mixtures of Mg or MgH2 with different proportions of Ag under Ar or H2 atmosphere.We observe that Ag and AgMg destabilize MgH2. In the first case the products of the reaction of Ag and MgH2 are AgMg and H2, in the second case MgH2 reacts with AgMg to give AgMg4 and H2. The first reaction was only observed in the forward direction, whereas the second one was registered in both directions. The impossibility to reverse the first reaction was attributed to poor kinetics and experimental limitations. The reversible destabilization induced by AgMg is low, MgH2 overall dehydriding enthalpy is reduced from 76.5 kJ/mol H2 to 69.1 kJ/mol H2. This last value allowed us to estimate the formation enthalpy of AgMg4 at _59.5 kJ/mol. Besides destabilization, a slight improvement in hydrogen absorption kinetics and a more noticeable enhancement in desorption kinetics has been observed in samples containing Ag as an additive. During thermal desorption, the dehydriding temperature decreases by 20 _C. In isothermal desorption experiments at 325 _C, the characteristic induction period of MgH2 without additive practically disappears, and the time to reach 50% of conversion decreases from 17 min to 5.4 min when silver is present. The changes in desorption kinetics could be attributed to AgMg or the interfaces MgH2/AgMg acting as nucleation sites for Mg. Fil: Urretavizcaya, Guillermina. Comisión Nacional de Energía Atómica. Gerencia del Área de Energía Nuclear. Instituto Balseiro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Sarmiento Chavez, Ana Carolina. Comisión Nacional de Energía Atómica. Gerencia del Área de Energía Nuclear. Instituto Balseiro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Castro, Facundo. Comisión Nacional de Energía Atómica. Gerencia del Área de Energía Nuclear. Instituto Balseiro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina |
description |
We analyze hydrogen absorption and desorption in Mg and Mg?Ag compounds prepared by mechanical milling. The materials were obtained by processing mixtures of Mg or MgH2 with different proportions of Ag under Ar or H2 atmosphere.We observe that Ag and AgMg destabilize MgH2. In the first case the products of the reaction of Ag and MgH2 are AgMg and H2, in the second case MgH2 reacts with AgMg to give AgMg4 and H2. The first reaction was only observed in the forward direction, whereas the second one was registered in both directions. The impossibility to reverse the first reaction was attributed to poor kinetics and experimental limitations. The reversible destabilization induced by AgMg is low, MgH2 overall dehydriding enthalpy is reduced from 76.5 kJ/mol H2 to 69.1 kJ/mol H2. This last value allowed us to estimate the formation enthalpy of AgMg4 at _59.5 kJ/mol. Besides destabilization, a slight improvement in hydrogen absorption kinetics and a more noticeable enhancement in desorption kinetics has been observed in samples containing Ag as an additive. During thermal desorption, the dehydriding temperature decreases by 20 _C. In isothermal desorption experiments at 325 _C, the characteristic induction period of MgH2 without additive practically disappears, and the time to reach 50% of conversion decreases from 17 min to 5.4 min when silver is present. The changes in desorption kinetics could be attributed to AgMg or the interfaces MgH2/AgMg acting as nucleation sites for Mg. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-05-22 |
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/11336/30867 Castro, Facundo; Sarmiento Chavez, Ana Carolina; Urretavizcaya, Guillermina; Hydrogen absorption and desorption in the Mg-Ag system; Elsevier Science Sa; Journal of Alloys and Compounds; 611; 2014; 22-5-2014; 202-209 0925-8388 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/30867 |
identifier_str_mv |
Castro, Facundo; Sarmiento Chavez, Ana Carolina; Urretavizcaya, Guillermina; Hydrogen absorption and desorption in the Mg-Ag system; Elsevier Science Sa; Journal of Alloys and Compounds; 611; 2014; 22-5-2014; 202-209 0925-8388 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0925838814011414?via%3Dihub info:eu-repo/semantics/altIdentifier/doi/10.1016/j.jallcom.2014.05.066 |
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 |
Elsevier Science Sa |
publisher.none.fl_str_mv |
Elsevier Science Sa |
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 |
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12.993085 |