Influence of Al Substitution and Crystal Size on the Room-Temperature Mössbauer Spectrum of Hematite

1986 ◽  
Vol 34 (1) ◽  
pp. 1-6 ◽  
Author(s):  
Enver Murad
Clay Minerals ◽  
1996 ◽  
Vol 31 (4) ◽  
pp. 455-464 ◽  
Author(s):  
J. Friedl ◽  
U. Schwertmann

AbstractTwo sets of natural Al-substituted goethites from contrasting surface environments (24 tropical and subtropical soils vs. ten lake iron ores from Finland) were characterized by Mössbauer spectra obtained at room temperature and 4.2 K. A negative correlation between Bhf and Al substitution (R2 = 0.751) was found by combining the data of all the samples, which was slightly improved (R2 = 0.779) by taking the mean coherence length perpendicular to 111 (MCL111) into account. The effect of Al on lowering Bhf was, however, stronger for the tropical soil goethites than for those of the lake ores. This is parallelled by a corresponding difference in the unit-cell decrease per unit Al substitution. These differences are believed to result from the crystallization conditions in the two different environments.


2010 ◽  
Vol 156-157 ◽  
pp. 1484-1487
Author(s):  
Hong Li Liu ◽  
Min Guo

We have systemically investigated mössbauer spectrum of R3Fe29-xCrx (R=Y, Gd, Tb, Dy) compound. Isomer shift、Quadrupole split and Hyperfine field at room temperature are studied. We know that the electronics transfer occurs between R and Fe atoms in the R3Fe29-xCrx compound.


1962 ◽  
Vol 17 (3) ◽  
pp. 248-259
Author(s):  
Michael Kalvius

The recoilless nuclear resonance absorption of the 8.42 kev γ-ray of Tm169 in the oxide crystal was investigated. The source (Er2O3) and the absorber (Tm203) were kept at room temperature. The measured MÖSSBAUER-spectrum indicates pure quadrupole splitting of the 8.42 kev nuclear level of Tm169 for the Thuliumions with a C2-symmetry as well as for those with C3i-symmetry. The energy of the electric interaction was found to beWel (C2) =8x 10-7 ev and Wel(C3i) =1.9 x 10 -6 ev.


Author(s):  
Harry A. Atwater ◽  
C.M. Yang ◽  
K.V. Shcheglov

Studies of the initial stages of nucleation of silicon and germanium have yielded insights that point the way to achievement of engineering control over crystal size evolution at the nanometer scale. In addition to their importance in understanding fundamental issues in nucleation, these studies are relevant to efforts to (i) control the size distributions of silicon and germanium “quantum dots𠇍, which will in turn enable control of the optical properties of these materials, (ii) and control the kinetics of crystallization of amorphous silicon and germanium films on amorphous insulating substrates so as to, e.g., produce crystalline grains of essentially arbitrary size.Ge quantum dot nanocrystals with average sizes between 2 nm and 9 nm were formed by room temperature ion implantation into SiO2, followed by precipitation during thermal anneals at temperatures between 30°C and 1200°C[1]. Surprisingly, it was found that Ge nanocrystal nucleation occurs at room temperature as shown in Fig. 1, and that subsequent microstructural evolution occurred via coarsening of the initial distribution.


1976 ◽  
Vol 37 (C6) ◽  
pp. C6-653-C6-655
Author(s):  
G. LANGOUCHE ◽  
B. B. TRIPLETT ◽  
N. S. DIXON ◽  
S. S. HANNA ◽  
P. BOOLCHAND

1974 ◽  
Vol 35 (C6) ◽  
pp. C6-309-C6-313
Author(s):  
M. KATO ◽  
Y. ISHIDA ◽  
K. SASSA ◽  
S. UMEYAMA ◽  
M. MORI

1978 ◽  
Vol 45 (2) ◽  
pp. K139-K143 ◽  
Author(s):  
J. V. de Menezes ◽  
F. de S. Barros

2017 ◽  
Vol 46 (31) ◽  
pp. 10433-10439 ◽  
Author(s):  
Qihua Zhou ◽  
Ruisheng Hu ◽  
Yun Jia ◽  
Hongye Wang

The Mossbauer spectrum and other characterization studies proved that the formation of KFeCl4 enhanced the catalytic performance for ethane oxychlorination.


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