Li4(NH2)3Cl amide-chloride: A new synthesis route, and hydrogen storage kinetic and thermodynamic properties
- Autores
- Gamba, Nadia Soledad; Arneodo Larochette, Pierre Paul; Gennari, Fabiana Cristina
- Año de publicación
- 2016
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Amide-halide compounds were identified as possible promoters of the dehydrogenation kinetics of the Li-N-H system. However, reversible hydrogen storage capacities and sorption kinetics of Li4(NH2)3Cl and Li3Mg0.5(NH2)3Cl have not been reported yet. In the present work, Li4(NH2)3Cl was synthesized using a new synthesis route that involves the pre-milling of a LiNH2-LiCl mixture. Attempts to synthesize Li3Mg0.5(NH2)3Cl by applying similar synthesis procedures using LiNH2 and 0.5MgCl2 were unsuccessful; instead, a mixture of Li4(NH2)3Cl-0.5Mg(NH2)2 was obtained. The hydrogen storage properties of the Li4(NH2)3Cl-3LiH and Li4(NH2)3Cl-0.5Mg(NH2)2-3LiH composites were evaluated between 200 °C and 300 °C. The onset of hydrogen release was reduced by 20 °C when Li4(NH2)3Cl-3LiH decomposed in the presence of Mg(NH2)2 (180 °C with respect to 200 °C) and its hydrogen desorption rate increased by 83%. However, no change in the dehydrogenation activation energy was observed for Li4(NH2)3Cl-3LiH decomposition due to minor amounts of Mg(NH2)2. The hydrogen storage capacity under cycling was reduced from about 3.0 wt% to 1.5 wt% at 300 °C, after rehydrogenation at 6.0 MPa. The formation of Li7(NH)3Cl was clearly identified in the dehydrogenated material. Unfortunately, the sloped plateau and the thermodynamic stability of Li4(NH2)3Cl-3LiH precludes its hydrogen storage applicability.
Fil: Gamba, Nadia Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Comisión Nacional de Energía Atómica. Centro Atómico Bariloche; Argentina
Fil: Arneodo Larochette, Pierre Paul. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Comisión Nacional de Energía Atómica. Centro Atómico Bariloche; Argentina. Comisión Nacional de Energía Atómica. Gerencia del Área de Energía Nuclear. Instituto Balseiro; Argentina
Fil: Gennari, Fabiana Cristina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Comisión Nacional de Energía Atómica. Centro Atómico Bariloche; Argentina. Comisión Nacional de Energía Atómica. Gerencia del Área de Energía Nuclear. Instituto Balseiro; Argentina - Materia
-
Hydrogen Storage
Amide-Chloride Compounds
Kinetic Properties
Thermodynamic Properties - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/60079
Ver los metadatos del registro completo
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Li4(NH2)3Cl amide-chloride: A new synthesis route, and hydrogen storage kinetic and thermodynamic propertiesGamba, Nadia SoledadArneodo Larochette, Pierre PaulGennari, Fabiana CristinaHydrogen StorageAmide-Chloride CompoundsKinetic PropertiesThermodynamic Propertieshttps://purl.org/becyt/ford/2.5https://purl.org/becyt/ford/2Amide-halide compounds were identified as possible promoters of the dehydrogenation kinetics of the Li-N-H system. However, reversible hydrogen storage capacities and sorption kinetics of Li4(NH2)3Cl and Li3Mg0.5(NH2)3Cl have not been reported yet. In the present work, Li4(NH2)3Cl was synthesized using a new synthesis route that involves the pre-milling of a LiNH2-LiCl mixture. Attempts to synthesize Li3Mg0.5(NH2)3Cl by applying similar synthesis procedures using LiNH2 and 0.5MgCl2 were unsuccessful; instead, a mixture of Li4(NH2)3Cl-0.5Mg(NH2)2 was obtained. The hydrogen storage properties of the Li4(NH2)3Cl-3LiH and Li4(NH2)3Cl-0.5Mg(NH2)2-3LiH composites were evaluated between 200 °C and 300 °C. The onset of hydrogen release was reduced by 20 °C when Li4(NH2)3Cl-3LiH decomposed in the presence of Mg(NH2)2 (180 °C with respect to 200 °C) and its hydrogen desorption rate increased by 83%. However, no change in the dehydrogenation activation energy was observed for Li4(NH2)3Cl-3LiH decomposition due to minor amounts of Mg(NH2)2. The hydrogen storage capacity under cycling was reduced from about 3.0 wt% to 1.5 wt% at 300 °C, after rehydrogenation at 6.0 MPa. The formation of Li7(NH)3Cl was clearly identified in the dehydrogenated material. Unfortunately, the sloped plateau and the thermodynamic stability of Li4(NH2)3Cl-3LiH precludes its hydrogen storage applicability.Fil: Gamba, Nadia Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Comisión Nacional de Energía Atómica. Centro Atómico Bariloche; ArgentinaFil: Arneodo Larochette, Pierre Paul. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Comisión Nacional de Energía Atómica. Centro Atómico Bariloche; Argentina. Comisión Nacional de Energía Atómica. Gerencia del Área de Energía Nuclear. Instituto Balseiro; ArgentinaFil: Gennari, Fabiana Cristina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Comisión Nacional de Energía Atómica. Centro Atómico Bariloche; Argentina. Comisión Nacional de Energía Atómica. Gerencia del Área de Energía Nuclear. Instituto Balseiro; ArgentinaRoyal Society of Chemistry2016-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/60079Gamba, Nadia Soledad; Arneodo Larochette, Pierre Paul; Gennari, Fabiana Cristina; Li4(NH2)3Cl amide-chloride: A new synthesis route, and hydrogen storage kinetic and thermodynamic properties; Royal Society of Chemistry; RSC Advances; 6; 19; 1-2016; 15622-156292046-2069CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1039/C5RA25271Ginfo:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2016/RA/C5RA25271Ginfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-11-05T10:51:48Zoai:ri.conicet.gov.ar:11336/60079instacron: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:34982025-11-05 10:51:49.18CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Li4(NH2)3Cl amide-chloride: A new synthesis route, and hydrogen storage kinetic and thermodynamic properties |
| title |
Li4(NH2)3Cl amide-chloride: A new synthesis route, and hydrogen storage kinetic and thermodynamic properties |
| spellingShingle |
Li4(NH2)3Cl amide-chloride: A new synthesis route, and hydrogen storage kinetic and thermodynamic properties Gamba, Nadia Soledad Hydrogen Storage Amide-Chloride Compounds Kinetic Properties Thermodynamic Properties |
| title_short |
Li4(NH2)3Cl amide-chloride: A new synthesis route, and hydrogen storage kinetic and thermodynamic properties |
| title_full |
Li4(NH2)3Cl amide-chloride: A new synthesis route, and hydrogen storage kinetic and thermodynamic properties |
| title_fullStr |
Li4(NH2)3Cl amide-chloride: A new synthesis route, and hydrogen storage kinetic and thermodynamic properties |
| title_full_unstemmed |
Li4(NH2)3Cl amide-chloride: A new synthesis route, and hydrogen storage kinetic and thermodynamic properties |
| title_sort |
Li4(NH2)3Cl amide-chloride: A new synthesis route, and hydrogen storage kinetic and thermodynamic properties |
| dc.creator.none.fl_str_mv |
Gamba, Nadia Soledad Arneodo Larochette, Pierre Paul Gennari, Fabiana Cristina |
| author |
Gamba, Nadia Soledad |
| author_facet |
Gamba, Nadia Soledad Arneodo Larochette, Pierre Paul Gennari, Fabiana Cristina |
| author_role |
author |
| author2 |
Arneodo Larochette, Pierre Paul Gennari, Fabiana Cristina |
| author2_role |
author author |
| dc.subject.none.fl_str_mv |
Hydrogen Storage Amide-Chloride Compounds Kinetic Properties Thermodynamic Properties |
| topic |
Hydrogen Storage Amide-Chloride Compounds Kinetic Properties Thermodynamic Properties |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/2.5 https://purl.org/becyt/ford/2 |
| dc.description.none.fl_txt_mv |
Amide-halide compounds were identified as possible promoters of the dehydrogenation kinetics of the Li-N-H system. However, reversible hydrogen storage capacities and sorption kinetics of Li4(NH2)3Cl and Li3Mg0.5(NH2)3Cl have not been reported yet. In the present work, Li4(NH2)3Cl was synthesized using a new synthesis route that involves the pre-milling of a LiNH2-LiCl mixture. Attempts to synthesize Li3Mg0.5(NH2)3Cl by applying similar synthesis procedures using LiNH2 and 0.5MgCl2 were unsuccessful; instead, a mixture of Li4(NH2)3Cl-0.5Mg(NH2)2 was obtained. The hydrogen storage properties of the Li4(NH2)3Cl-3LiH and Li4(NH2)3Cl-0.5Mg(NH2)2-3LiH composites were evaluated between 200 °C and 300 °C. The onset of hydrogen release was reduced by 20 °C when Li4(NH2)3Cl-3LiH decomposed in the presence of Mg(NH2)2 (180 °C with respect to 200 °C) and its hydrogen desorption rate increased by 83%. However, no change in the dehydrogenation activation energy was observed for Li4(NH2)3Cl-3LiH decomposition due to minor amounts of Mg(NH2)2. The hydrogen storage capacity under cycling was reduced from about 3.0 wt% to 1.5 wt% at 300 °C, after rehydrogenation at 6.0 MPa. The formation of Li7(NH)3Cl was clearly identified in the dehydrogenated material. Unfortunately, the sloped plateau and the thermodynamic stability of Li4(NH2)3Cl-3LiH precludes its hydrogen storage applicability. Fil: Gamba, Nadia Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Comisión Nacional de Energía Atómica. Centro Atómico Bariloche; Argentina Fil: Arneodo Larochette, Pierre Paul. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Comisión Nacional de Energía Atómica. Centro Atómico Bariloche; Argentina. Comisión Nacional de Energía Atómica. Gerencia del Área de Energía Nuclear. Instituto Balseiro; Argentina Fil: Gennari, Fabiana Cristina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Comisión Nacional de Energía Atómica. Centro Atómico Bariloche; Argentina. Comisión Nacional de Energía Atómica. Gerencia del Área de Energía Nuclear. Instituto Balseiro; Argentina |
| description |
Amide-halide compounds were identified as possible promoters of the dehydrogenation kinetics of the Li-N-H system. However, reversible hydrogen storage capacities and sorption kinetics of Li4(NH2)3Cl and Li3Mg0.5(NH2)3Cl have not been reported yet. In the present work, Li4(NH2)3Cl was synthesized using a new synthesis route that involves the pre-milling of a LiNH2-LiCl mixture. Attempts to synthesize Li3Mg0.5(NH2)3Cl by applying similar synthesis procedures using LiNH2 and 0.5MgCl2 were unsuccessful; instead, a mixture of Li4(NH2)3Cl-0.5Mg(NH2)2 was obtained. The hydrogen storage properties of the Li4(NH2)3Cl-3LiH and Li4(NH2)3Cl-0.5Mg(NH2)2-3LiH composites were evaluated between 200 °C and 300 °C. The onset of hydrogen release was reduced by 20 °C when Li4(NH2)3Cl-3LiH decomposed in the presence of Mg(NH2)2 (180 °C with respect to 200 °C) and its hydrogen desorption rate increased by 83%. However, no change in the dehydrogenation activation energy was observed for Li4(NH2)3Cl-3LiH decomposition due to minor amounts of Mg(NH2)2. The hydrogen storage capacity under cycling was reduced from about 3.0 wt% to 1.5 wt% at 300 °C, after rehydrogenation at 6.0 MPa. The formation of Li7(NH)3Cl was clearly identified in the dehydrogenated material. Unfortunately, the sloped plateau and the thermodynamic stability of Li4(NH2)3Cl-3LiH precludes its hydrogen storage applicability. |
| publishDate |
2016 |
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2016-01 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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article |
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publishedVersion |
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http://hdl.handle.net/11336/60079 Gamba, Nadia Soledad; Arneodo Larochette, Pierre Paul; Gennari, Fabiana Cristina; Li4(NH2)3Cl amide-chloride: A new synthesis route, and hydrogen storage kinetic and thermodynamic properties; Royal Society of Chemistry; RSC Advances; 6; 19; 1-2016; 15622-15629 2046-2069 CONICET Digital CONICET |
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http://hdl.handle.net/11336/60079 |
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Gamba, Nadia Soledad; Arneodo Larochette, Pierre Paul; Gennari, Fabiana Cristina; Li4(NH2)3Cl amide-chloride: A new synthesis route, and hydrogen storage kinetic and thermodynamic properties; Royal Society of Chemistry; RSC Advances; 6; 19; 1-2016; 15622-15629 2046-2069 CONICET Digital CONICET |
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eng |
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eng |
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Royal Society of Chemistry |
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