P.R. Palacios, A. Bustamante, P. Romero-Gómez, J.C. González
Hyperfine Interact, 203 (2011) 113-118
doi: 10.1007/s10751-011-0352-2

A kinetic study about the phase limonite (FeO(OH)-nH₂O) was performed through X-ray diffraction, μ-Raman spectroscopy and Mössbauer spectroscopy. The oxide powder sample was extracted from Taraco district, Huancané province of Puno (Peru). X-ray diffraction identified the phase goethite as the main mineralogical component, and then the sample was subjected to in-situ heat treatment in the temperature range: 100 to 500°C in oxidizing (air) and inert (nitrogen) atmospheres. The goethite phase remains stable in this range: room temperature to 200°C. Between 200°C to 250°C there is a phase transition: α-Fe^3 +O(OH) → α-Fe₂O₃, i.e., from goethite to hematite phase, taking as evidence the evolution of the diffraction profiles. At 200°C spectra shows the start of broadened magnetic component and it was adjusted through of a magnetic distribution giving a mean field of 38.6T and a relative area of 52.9%, which is a characteristic of goethite. Also, it is noticed the presence of a small amount of hematite with a mean field of 49.0T linked with a superparamagnetic broadened doublet of relative area of 47.1% where the domains of the particles have sizes smaller than 100 Å and it is evidence the superparamagnetic limit; i.e., the superparamagnetic effect tends toward a distribution of magnetic fields. Moreover, the Raman spectra of the in-situ thermal treatment, support the transition at 290°C through the transformation of characteristic bands of goethite to hematite phase at the frequency range from 200 to 1,800 cm^− 1.