Octahedral cation distribution in glauconites from Southern Urals by combination of crystal-chemical model and quasi-continuous model-independent quadrupole splitting distributions (QSD) fitted to their Mössbauer spectra

2013 ◽  
Vol 25 (3) ◽  
pp. 405-414 ◽  
Author(s):  
Lidia G. Dainyak ◽  
Viacheslav S. Rusakov ◽  
Ivan A. Sukhorukov ◽  
Victor A. Drits
Clay Minerals ◽  
1984 ◽  
Vol 19 (1) ◽  
pp. 77-83 ◽  
Author(s):  
E. Murad ◽  
R. M. Taylor

AbstractMössbauer spectra of Fe2+Fe3+ and Fe2+Al hydroxycarbonates taken in the paramagnetic state were fitted using two Fe2+ and Fe3+ doublets each. These spectra can be interpreted in terms of an ordered cation arrangement in the pyroaurite-type structure. The inner Fe2+ doublet seems to be the outcome of excess Fe3+ in the samples studied. The outer Fe2+ doublet (quadrupole splitting ∼2·8 mm s−1, FWHM = 0·26 mm s−1) is relatively well-defined and can, together with the fact that this doublet disappears on oxidation, possibly serve to identify these compounds in natural systems.


2015 ◽  
Vol 70 (10) ◽  
pp. 765-767
Author(s):  
Birgit Gerke ◽  
Thanh Thao Tran ◽  
Rainer Pöttgen ◽  
P. Shiv Halasyamani

AbstractThe complex Sn(II) fluorides ASnF3 (A = Na, K, Rb, Cs) were synthesized from the alkali fluorides and SnF2 in methanol through a solvothermal route. Their 119Sn Mössbauer spectra manifest divalent tin. The isomer shifts range from 3.09 to 2.94 mm s–1. The pronounced lone-pair character at the Sn(II) centres is expressed by strong electric quadrupole splitting (1.91–1.95 mm s–1). The two, respectively four crystallographically independent tin sites in NaSnF3, KSnF3 and RbSnF3 could not be resolved in the 119Sn spectra.


1973 ◽  
Vol 59 (2) ◽  
pp. 707-714 ◽  
Author(s):  
I. B. Bersuker ◽  
S. A. Borshch ◽  
I. Ya. Ogurtsov

1971 ◽  
Vol 24 (11) ◽  
pp. 2231 ◽  
Author(s):  
RL Martin ◽  
IAG Roos

The temperature dependence of the Mossbauer spectra of some iron- containing compounds of dithioacetylacetone are reported between 4 and 293 K. ��� The quadrupole splitting ΔEq of [Fe(SacSac)3] is larger than usually observed for low-spin six-coordinated iron(III) and is ascribed to the lifting of orbital degeneracy of the 2T2 ground state by small axial and rhombic distortions. ��� The unsubstituted and phenyl-substituted dithiolium salts of [FeCl4]2- exhibit strongly temperature-dependent quadrupole splittings, which arise directly from the lifting of the orbital degeneracy of the 5E ground state due to distortion of the [FeCl4]2- tetrahedron.


2000 ◽  
Vol 55 (1-2) ◽  
pp. 193-198 ◽  
Author(s):  
M. I. Oshtrakh ◽  
O. B. Milder ◽  
V. A. Semionkin ◽  
A. L. Berkovsky ◽  
M. A. Azhigirova ◽  
...  

Human adult hemoglobin modified by both pyridoxal-5'-phosphate and glutaraldehyde in the oxy-form was studied by Mössbauer spectroscopy. Mössbauer spectra were measured at 87 and 295 K (hemoglobin in lyophilized form) and at 87 K (hemoglobin in frozen solution). The values of the quadrupole splitting for modified oxyhemoglobin were found to be lower then those of oxyhemoglobin without modifications in lyophilized form and frozen solution, respectively. The Mössbauer spectra of modified oxyhemoglobin were also analyzed in terms of the heme iron inequivalence in α-and β-subunits of the tetramer. Differences of the tendencies of temperature dependencies of quadrupole splitting for modified and non-modified oxyhemoglobin in lyophilized form were shown.


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