High temperature Mössbauer spectroscopy of titanomagnetite and maghemite in basalts

1994 ◽  
Vol 91 (1) ◽  
pp. 595-599 ◽  
Author(s):  
ö. Helgason ◽  
H. P. Gunnlaugsson ◽  
K. Jónsson ◽  
S. Steinthórsson
1990 ◽  
Vol 42 (4) ◽  
pp. 2188-2192 ◽  
Author(s):  
M. G. Smith ◽  
R. D. Taylor ◽  
M. P. Pasternak ◽  
H. Oesterreicher

2003 ◽  
Vol 629 (10) ◽  
pp. 1787-1794 ◽  
Author(s):  
V. Ksenofontov ◽  
S. Reiman ◽  
M. Waldeck ◽  
R. Niewa ◽  
R. Kniep ◽  
...  

1993 ◽  
Vol 15 (3-4) ◽  
pp. 211-224 ◽  
Author(s):  
E. Kuzmann ◽  
Z. Homonnay ◽  
S. Nagy ◽  
M. Gál ◽  
A. Vértes

57Fe,119Sn, and151Eu Mössbauer spectroscopy was used to study the chemical structure, phonon mode changes, and low-temperature phase transformation around the Tcas well as suppression of superconductivity in high-temperature superconductors and related compounds. Anomalous temperature-dependent changes in the total57Fe spectral area fraction and in the Mössbauer line shift were simultaneously found around the Tcin a EuBa2(Cu0.9957Fe0.01)3O7-dsuperconductor. These anomalous changes were attributed to phonon softening and low-temperature phase transformation occurring around the superconducting transition. Significant differences were observed between the57Fe Mössbauer spectra of superconducting EuBa2(Cu0.9957Fe0.01)3O7-dand the isostructural non-superconducting PrBa2(Cu0.9957Fe0.01)3O7-d. The differences were interpreted in connection with the suppression of superconductivity (by hole filling or hybridization of Pr, Cu and O states) in the Pr-containing compound. The unusually high isomer shift value observed in the Pr-containing material can give evidence for the charge transfer mechanism between the Cu(1) chains and the Cu(2) planes and for its role in the suppression of superconductivity.


1992 ◽  
Vol 56 (383) ◽  
pp. 185-199 ◽  
Author(s):  
S. Steinthorsson ◽  
Ö. Helgason ◽  
M. B. Madsen ◽  
C. Bender Koch ◽  
M. D. Bentzon ◽  
...  

AbstractCurie temperatures indicating non-titaniferous magnetite are common in Icelandic basalts of all ages, especially Tertiary ones. Yet, microprobe analyses of such samples have shown high titanium in the magnetite. To resolve this paradox, and the mechanism at work, the magnetic mineral fraction of eight basalt samples with Js-T curves characteristic for pure magnetite was subjected to a multi-disciplinary analysis including Mössbauer spectroscopy and X-ray diffraction. In most of the samples titanium in the magnetite, as analysed with the microprobe, ranged between 16 and 28 wt.%, indicating submicroscopic solvus exsolution in the titanomagnetite, beyond the power of resolution for the microprobe. More unexpectedly in view of the reversible Js-T curves, Mössbauer spectroscopy showed appreciable proportion of maghemite in the magnetic fraction. A three-stage mechanism is proposed for the formation of the mineral assemblages observed: (1) limited high-temperature oxyexsolution; (2) solvus exsolution during low-temperature hydrothermal alteration; and (3) maghemitization of the magnetite. Finally, the maghemite may transform to hematite with time. It is concluded that maghemite is much more common in Icelandic rocks than hitherto believed.


Author(s):  
Yaroslav P. Biryukov ◽  
Almaz L. Zinnatullin ◽  
Rimma S. Bubnova ◽  
Farit G. Vagizov ◽  
Andrey P. Shablinskii ◽  
...  

The investigation of elemental composition, crystal structure and thermal behavior of vonsenite and hulsite from the Titovskoe boron deposit in Russia is reported. The structures of the borates are described in terms of cation-centered and oxocentred polyhedra. There are different sequences of double chains and layers consisting of oxocentred [OM 4] n + tetrahedra and [OM 5] n + tetragonal pyramids forming a framework. Elemental composition was determined by energy-dispersive X-ray spectroscopy (EDX). Oxidation states and coordination sites of iron and tin in the oxoborates are determined using Mössbauer spectroscopy and compared with EDX and X-ray diffraction data (XRD). According to results obtained from high-temperature Mössbauer spectroscopy, the Fe2+ to Fe3+ oxidation in vonsenite and hulsite occurs at approximately 500 and 600 K, respectively. According to the high-temperature XRD data, this process is accompanied by an assumed deformation of crystal structures and subsequent solid-phase decomposition to hematite and warwickite. It is seen as a monotonic decrease of volume thermal expansion coefficients with an increase in temperature. A partial magnetic ordering in hulsite is observed for the first time with T c ≃ 383 K. Near this temperature, an unusual change of thermal expansion coefficients is revealed. Vonsenite starts to melt at 1571 K and hulsite melts at 1504 K. Eigenvalues of thermal expansion tensor are calculated for the oxoborates as well as anisotropy of the expansion is described in comparison with their crystal structures.


CORROSION ◽  
10.5006/2676 ◽  
2018 ◽  
Vol 74 (6) ◽  
pp. 623-634 ◽  
Author(s):  
Rafał Idczak ◽  
Karolina Idczak ◽  
Robert Konieczny

The high-temperature corrosion behavior of three polycrystalline Fe-Si alloys containing approximately 4, 5, and 10 at% Si was studied using transmission Mössbauer spectroscopy (TMS), conversion electron Mössbauer spectroscopy (CEMS), and x-ray photoelectron spectroscopy (XPS). The XPS measurements reveal the strong segregation process of silicon atoms to the surface. Moreover, the obtained XPS results suggest that the presence of adsorbed oxygen on the Fe-Si surface effectively enhances the silicon segregation process. On the other hand, the obtained TMS and CEMS spectra show that even 10% of silicon atoms dissolved in the iron matrix do not prevent high-temperature corrosion of the studied Fe-Si alloys. During exposure to air at 870 K, a systematic growth of an α-Fe2O3 compound was observed. Finally, the Mössbauer results show that, during exposure to air, oxygen atoms diffuse to the studied polycrystalline materials not only through the oxide/metal interface on the surface but also along the grain boundaries. Such effects result in the formation of iron oxides in deeper parts of the alloy.


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