Study by Mössbauer-Spectroscopy of Iron Oxides in Acid-Resistant Ceramic Materials Based on Production Waste

2020 ◽  
Vol 61 (2) ◽  
pp. 183-187
Author(s):  
A. K. Kairakbaev ◽  
V. Z. Abdrakhimov ◽  
E. S. Abdrakhimova
1973 ◽  
Vol 13 (12) ◽  
pp. 933-938 ◽  
Author(s):  
D.A. Channing ◽  
S.M. Dickerson ◽  
M.J. Graham

2021 ◽  
Vol 25 (3) ◽  
pp. 263-273
Author(s):  
Brahiam Hincapié ◽  
Alexander Cortés-Soto ◽  
Mauricio A Bermudez ◽  
Santiago Yepez ◽  
Juan Sebastián Trujillo-Hernández ◽  
...  

The presence of iron oxides may provide a sensitive indicator of the effects of cropping practices on coffee plantations. Authors characterized the mineral phases present in soil A horizons at three different farms located in the Department of Tolima within the regions of Líbano and Villahermosa. Our analysis includes X-ray diffraction, Mössbauer spectroscopy, and remote sensing to discriminate the distribution of the different magnetic mineral phases. X-ray diffraction was used to identify the mineralogical properties of iron oxide such as hematite, goethite, and ferrihydrite (Fh), as well as tectosilicate minerals such as albite and sanidine. Mössbauer spectroscopy results for samples taken at room temperature indicate the presence of Fe2+ and Fe3+ mineral phases, which possibly correspond to ilmenite or magnetite. Finally, Sentinel-2A multi-spectral imager (MSI) data was used to map the distribution of iron oxides and study the influence of their distribution throughout the study area. A high correlation between Mössbauer spectroscopy and Sentinel-2A MSI data exists throughout the study area. The results suggest that farms close to the main Nevado del Ruíz Volcano have a more significant mineralogical variability. In contrast, more distant farms are characterized by soils with more iron oxides, the product of weathering, erosion, and human activities.


Clay Minerals ◽  
1994 ◽  
Vol 29 (1) ◽  
pp. 1-10 ◽  
Author(s):  
E. Murad ◽  
U. Wagner

AbstractEight illites were studied by Mössbauer spectroscopy at room temperature and 4.2 K. On the basis of their Fe contents, these illites can be divided into an Fe-rich (>5 wt% Fe) and an Fe-poor (<1 to ∼3 wt% Fe) group. Mössbauer spectroscopy showed that the Fe-rich illites had lower proportions of divalent Fe than their Fe-poor counterparts. Slow paramagnetic relaxation was observed in the Fe-poor illites and must be accounted for when fitting the spectra. Two samples contained iron oxides that were superparamagnetic and thus, although contributing to the Fe3+ doublets, escaped detection at room temperature. Structural Fe3+ had a temperature-independent quadrupole splitting that was lower for the Fe-rich illites (0.59 mm/s) than that of the Fe-poor illites (0.73 mm/s). The Fe2+ quadrupole splittings were higher at 4.2 K than at room temperature, but the Fe-rich illites again had lower Fe2+ quadrupole splittings both at room temperature (2.69 vs. 2.88 mm/s) and at 4.2 K (2.96 mm/s vs. 3.08 mm/s). Distinction of Fe sites in the illites with cis- and trans-OH coordination was not possible. The presence of tetrahedral Fe3+ was observed only in the most Fe-rich sample (8.4 wt% Fe).


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