Pregled bibliografske jedinice broj: 36053
The RENi4Ga (RE=Dy,Ho,Er) intermetallic compounds - crystal structure and hydride properties
The RENi4Ga (RE=Dy,Ho,Er) intermetallic compounds - crystal structure and hydride properties // Croatica chemica acta, 72 (1999), 2-3; 567-574 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 36053 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
The RENi4Ga (RE=Dy,Ho,Er) intermetallic compounds - crystal structure and hydride properties
Autori
Šorgić, Božica ; Blažina, Želimir ; Drašner, Antun
Izvornik
Croatica chemica acta (0011-1643) 72
(1999), 2-3;
567-574
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
rare earth intermetallics; hydrogen sorption; crystal structure; thermodynamic properties
(rare earth intermatallics; hydrogen sorption; crystal structure; thermodynamic properties)
Sažetak
New ternary rare earth based intermetallic compounds of the composition RENi4Ga (RE=Dy,Ho,Er) were prepared and studied using X-ray powder diffraction. All compounds were found to be hexagonal and to crystallize in the space group P6/mmm with the CaCu5 type of structure, i.e., the same symmetry as their prototype binaries RENi5. The interaction with hydrogen was also studied. It was found that all intermatallics react readily and reversibly with hydrogen to form hydrides with hydrogen contents of up to 3.48 hydrogen atoms per alloy formula unit at room temperature. The entropy, the enthalpy and the Gibbs free energy of formation have been extracted from the equilibrium plateau in the pressure composition desorption isotherms. The thermodynamic parameters and the hydrogen capacity of the RENi4Ga-hydrogen systems are compared with the corresponding values for their aluminium analogues and briefly discussed.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus