Ternary Mg–Nb2O5 – graphitic C mixtures (molar ratio % = 97.5:0.5:2.0) were prepared by high-energy ball milling (BM) under Ar for different times (from 0.25 h to 4 h) and thoroughly characterized by manometric, calorimetric, X-ray powder diffraction, and scanning electron microscopy analyses. The aims of the work were: - to assess the effect of the simultaneous presence of the two dopants on the reactivity and the sorption properties of the Mg–MgH2 system; - to study the influence of the milling time on the performance of the mixtures. Neither milling nor the high temperature/high pressure treatments led to reactions among the components of the mixtures, and Mg was the only hydrogen active phase. After 4 activation cycles at 623 K and 35 bar/1 bar charging/discharging pressure, the mixture milled for 1 h was the best performing one: it reversibly charged up to 6.8 wt% H2 with absorption/desorption rates 64/4.5 times higher than those of a pure Mg sample BM for the same time and activation energies 3.6/2 times lower. The desorption temperature and the dehydrogenation enthalpy of the ternary mixture were respectively 40 K and 4 kJ/mol H2 lower than those of pure MgH2.

Synergetic effect of C (graphite) and Nb2O5 on the H2 sorption properties of the Mg-MgH2 system

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

Abstract

Ternary Mg–Nb2O5 – graphitic C mixtures (molar ratio % = 97.5:0.5:2.0) were prepared by high-energy ball milling (BM) under Ar for different times (from 0.25 h to 4 h) and thoroughly characterized by manometric, calorimetric, X-ray powder diffraction, and scanning electron microscopy analyses. The aims of the work were: - to assess the effect of the simultaneous presence of the two dopants on the reactivity and the sorption properties of the Mg–MgH2 system; - to study the influence of the milling time on the performance of the mixtures. Neither milling nor the high temperature/high pressure treatments led to reactions among the components of the mixtures, and Mg was the only hydrogen active phase. After 4 activation cycles at 623 K and 35 bar/1 bar charging/discharging pressure, the mixture milled for 1 h was the best performing one: it reversibly charged up to 6.8 wt% H2 with absorption/desorption rates 64/4.5 times higher than those of a pure Mg sample BM for the same time and activation energies 3.6/2 times lower. The desorption temperature and the dehydrogenation enthalpy of the ternary mixture were respectively 40 K and 4 kJ/mol H2 lower than those of pure MgH2.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/213542
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