Estimation of the exchange constants in the Fe sublattice of the Y2Fe17 and Y2Fe17N3−δ compounds from the analysis of Mössbauer measurements

1994 ◽  
Vol 130 (1-3) ◽  
pp. 57-62 ◽  
Author(s):  
M.S. Anagnostou ◽  
I. Panagiotopoulos ◽  
A. Kostikas ◽  
D. Niarchos ◽  
G. Zouganelis
1995 ◽  
Vol 5 (4) ◽  
pp. 501-515 ◽  
Author(s):  
J. A. Hodges ◽  
P. Bonville ◽  
P. Imbert ◽  
A. Pinatel-Phillipot

1996 ◽  
Vol 33 (8) ◽  
pp. 71-77
Author(s):  
I. M.-C. Lo ◽  
H. M. Liljestrand ◽  
J. Khim ◽  
Y. Shimizu

Simple land disposal systems for hazardous and mixed wastes contain heavy metal cationic species through precipitation and ion exchange mechanisms but typically fail by releasing soluble organic and inorganic anionic species. To enhance the removal of anions from leachate, clays are modified with coatings of iron or aluminium cations to bridge between the anionic surface and the anionic pollutants. A competitive surface ligand exchange model indicates that surface coatings of 10 meq cation/gm montmorillonite under typical leachate conditions increase the inorganic anion sorption capacity by at least a factor of 6 and increase the intrinsic surface exchange constants by more than a factor of 100. Similarly, metal hydroxide coatings on montmorillonite increase the organic anion sorption capacity by a factor of 9 and increase the intrinsic surface exchange constants by a factor of 20. For historical concentrations of non-metal anions in US hazardous and mixed waste leachate, sorption onto natural clay liner materials is dominated by arsenate sorption. With cation coatings, anion exchange provides an effective removal for arsenate, selenate, phenols, cresols, and phthalates. Engineering applications are presented for the use of modified clays as in situ barriers to leachate transport of anionic pollutants as well as for above ground treatment of recovered leachate.


Nanomaterials ◽  
2019 ◽  
Vol 10 (1) ◽  
pp. 26 ◽  
Author(s):  
Manel Missaoui ◽  
Sandrine Coste ◽  
Maud Barré ◽  
Anthony Rousseau ◽  
Yaovi Gagou ◽  
...  

Exclusive and unprecedented interest was accorded in this paper to the synthesis of BiFeO3 nanopowders by the polyol process. The synthesis protocol was explored and adjusted to control the purity and the grain size of the final product. The optimum parameters were carefully established and an average crystallite size of about 40 nm was obtained. XRD and Mössbauer measurements proved the high purity of the synthesized nanostructurated powders and confirmed the persistence of the rhombohedral R3c symmetry. The first studies on the magnetic properties show a noticeable widening of the hysteresis loop despite the remaining cycloidal magnetic structure, promoting the enhancement of the ferromagnetic order and consequently the magnetoelectric coupling compared to micrometric size powders.


Polyhedron ◽  
2000 ◽  
Vol 19 (2) ◽  
pp. 205-210 ◽  
Author(s):  
Satoru Nakashima ◽  
Naoki Ichikawa ◽  
Hiroaki Komatsu ◽  
Koji Yamada ◽  
Tsutomu Okuda

1984 ◽  
Vol 62 (3) ◽  
pp. 591-595 ◽  
Author(s):  
Thomas Birchall ◽  
Georges Dénès

19F and 119Sn nmr spectroscopy has been used to study the SnF2–MF–H2O (M = Li+, Na+, K+, Rb+, Cs+, and [NH4]+) system. The nmr data have been supplemented by frozen solution 119Sn Mössbauer measurements. The evidence suggests that the dominant species in the SnF2–H2O system is a hydrated stannous fluoride, probably SnF2•H2O having Mössbauer parameters of δ = 3.46 mm s−1 and Δ = 1.70 mm s−1. When F− is added to these solutions rapid F− exchange occurs with the hydrated SnF2 and the dominant species becomes [SnF3]−. The 119Sn nmr chemical shift of [SnF3]− is ~ −700 ppm from (CH3)4Sn. The 119Sn Mössbauer parameters for frozen solutions of [SnF3]− are δ = ~ 3.1 mm s−1 Δ = 1.9 mm s−1. These spectroscopic data are cation dependent. We could find no strong evidence for high concentrations of [Sn2F5]− in any of these solutions.


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