T. Togawa et al., THE EFFECT OF THE CRYSTAL ORIENTATION ON THE RATE OF FORMATION OF CATION-EXCESS MAGNETITE, Solid state ionics, 89(3-4), 1996, pp. 279-286
Cation-excess magnetite (Fe3O4-delta) has been found to form by passin
g H-2 gas through magnetite powder at 300 degrees C with its spinel st
ructure retained. Cation-excess magnetite is' a metastable phase in th
e transformation of magnetite into alpha-Fe. The lattice constant of t
he cation-excess magnetite was enlarged to a maximum value of 0.8407 n
m, which is substantially larger than that of stoichiometric magnetite
(a(0) = 0.8396 nm). The formation mechanism of cation-excess magnetit
e in the spinel structure was studied using two specimens of magnetite
crystals with (111) and (100) planes developed. They were referred to
as (111)- and (100)-magnetite. The formation of alpha-Fe was decrease
d over the former, where wustite and cation-excess magnetite were form
ed while keeping the fee arrangement of the oxide ions in the solid. O
n the other hand, alpha-Fe was more easily formed over the latter. It
is considered that the cation excess state can appear when lattice oxy
gen is removed faster than the formation of Fe2+ ions coming from Fe3 ions through the H-2 reduction and that the cation excess state is st
abilized due to electron hopping between Fe2+ and Fe3+ ions in the B s
ite of the spinel structure.