Mg-based ternary mixtures (Mg wt% in the range 40% - 80%) containing increasing amount (up to 30 wt %) of Ni and Cu were prepared by ball milling (BM) under Ar for 16 h and subsequently activated at high temperature (623 K) by charging/discharging cycles at H2 pressure of 50 bar/0.7 bar. The work aims to analyze the influence of the mixtures’ composition on the storage properties (H2 intake and sorption kinetics) and to describe the role played by an ad-hoc activation in reaching these same properties. The storage capacity of the mixtures decreases by decreasing the Mg starting content, the H2 active phases being ‘‘free Mg’’ and the ‘‘bonded Mg’’ intermetallic compounds Mg2Ni and Mg2Cu. After full activation (3 charging/ discharging runs), ‘‘free Mg’’ hydrogenates 10 times quicker than the ‘‘bonded Mg phases’’, while the discharging of both ‘‘free’’ and ‘‘bonded’’ Mg hydrides takes place simultaneously with similar kinetics. The best kinetic performance is shown by the samples with Mg = 60 wt% and 70 wt% and the highest Ni content (30% and 20% respectively), with sorption rates up to 7 times higher than those of the pure Mg/ MgH2 system.

Mg – Ni – Cu mixtures for hydrogen storage: a kinetic study

MILANESE, CHIARA;BRUNI, GIOVANNA;COFRANCESCO, PACIFICO;BERBENNI, VITTORIO;MARINI, AMEDEO
2010-01-01

Abstract

Mg-based ternary mixtures (Mg wt% in the range 40% - 80%) containing increasing amount (up to 30 wt %) of Ni and Cu were prepared by ball milling (BM) under Ar for 16 h and subsequently activated at high temperature (623 K) by charging/discharging cycles at H2 pressure of 50 bar/0.7 bar. The work aims to analyze the influence of the mixtures’ composition on the storage properties (H2 intake and sorption kinetics) and to describe the role played by an ad-hoc activation in reaching these same properties. The storage capacity of the mixtures decreases by decreasing the Mg starting content, the H2 active phases being ‘‘free Mg’’ and the ‘‘bonded Mg’’ intermetallic compounds Mg2Ni and Mg2Cu. After full activation (3 charging/ discharging runs), ‘‘free Mg’’ hydrogenates 10 times quicker than the ‘‘bonded Mg phases’’, while the discharging of both ‘‘free’’ and ‘‘bonded’’ Mg hydrides takes place simultaneously with similar kinetics. The best kinetic performance is shown by the samples with Mg = 60 wt% and 70 wt% and the highest Ni content (30% and 20% respectively), with sorption rates up to 7 times higher than those of the pure Mg/ MgH2 system.
2010
Materials Science and Engineering is concerned with admixtures of matter or the basic matter from which products are made. The category covers ceramics, paper and wood products, polymers, textiles, composites, coatings & films, and biomaterials. Other areas covered in this category include Materials Chemistry, the application of chemistry to materials design and testing; Condensed Matter/Solid State Physics, the branch of physics concerned with the structure and properties of condensed matter (superconductors, semiconductors, ferroelectrics, and dielectrics); and Physical Chemistry/Chemical Physics, the application of the concepts and laws of physics to chemical phenomena.
The Physical Chemistry/Chemical Physics category includes resources on photochemistry, solid state chemistry, kinetics, catalysis, quantum chemistry, surface chemistry, electro-chemistry, chemical thermodynamics, thermo-physics, colloids, fullerenes and zeolites. Resources dealing with (liquid) crystals and crystallography are also included in this category. This category also includes resources on atomic, molecular and chemical physics, which concerns the structure of atoms and molecules, atomic and molecular interactions with radiation, magnetic resonance and relaxation, Mossbauer effect, and atomic and molecular collision processes and interactions.
Sì, ma tipo non specificato
Inglese
Internazionale
STAMPA
18
203
211
9
Hydrogen storage; Mechanical alloying and milling; Diffraction
7
info:eu-repo/semantics/article
262
Milanese, Chiara; Girella, Alessandro; Bruni, Giovanna; Cofrancesco, Pacifico; Berbenni, Vittorio; Matteazzi, Paolo; Marini, Amedeo
1 Contributo su Rivista::1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/203555
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