scholarly journals Mössbauer study of treated Nd2Fe14B

Nukleonika ◽  
2015 ◽  
Vol 60 (1) ◽  
pp. 7-10 ◽  
Author(s):  
Mieczysław Budzyński ◽  
Virgil C. Constantin ◽  
Ana-Maria J. Popescu ◽  
Zbigniew Surowiec ◽  
Tamara M. Tkachenka ◽  
...  

Abstract The Nd2Fe14B cylindrical magnets were treated with water solutions of alkali, acid, and salt. Mössbauer spectroscopy was applied to study the composition and properties of the surface material of the treated magnets. It is shown that the main phase of the permanent Nd2Fe14B magnet partly decomposes. The released α-Nd at the grain boundaries interacts with water and forms neodymium hydroxide matrix, and the released Fe diffuses into it. The presence of Fe-Nd(OH)3 is reflected in the paramagnet doublet in the Mössbauer spectra of treated neodymium magnets.

2016 ◽  
Vol 2016 ◽  
pp. 1-6 ◽  
Author(s):  
Łukasz Laskowski ◽  
Magdalena Laskowska ◽  
Jerzy Jelonkiewicz ◽  
Tomasz Galkowski ◽  
Piotr Pawlik ◽  
...  

Mesoporous silica SBA-15 containing propyl-iron-phosphonate groups were considered to confirm their molecular structure. To detect the iron-containing group configuration the Mössbauer spectroscopy was used. Both mesoporous silica SBA-15 containing propyl-iron-phosphonate groups and pure doping agent (iron acetylacetate) were investigated using Mössbauer spectroscopy. The parameters such as isomer shift, quadrupole splitting, and asymmetry in57Fe Mössbauer spectra were analyzed. The differences in Mössbauer spectra were explained assuming different local surroundings of Fe nuclei. On this base we were able to conclude about activation of phosphonate units by iron ions and determinate the oxidation state of the metal ion. To examine bonding between iron atoms and phosphonic units the resonance Raman spectroscopy was applied. The density functional theory (DFT) approach was used to make adequate calculations. The distribution of active units inside silica matrix was estimated by comparison of calculated vibrational spectra with the experimental ones. Analysis of both Mössbauer and resonance Raman spectra seems to confirm the correctness of the synthesis procedure. Also EDX elemental analysis confirms our conclusions.


Author(s):  
Amel Kaibi ◽  
Abderrahim Guittoum ◽  
Nassim Souami ◽  
Mohamed Kechouane

Nanocrystalline Ni75Fe25 (Ni3Fe) powders were prepared by mechanical alloying process using a vario-planetary high-energy ball mill. The intermetallic Ni3Fe formation and different physical properties were investigated, as a function of milling time, t, (in the range 6 to 96 h range), using X-Ray Diffraction (XRD) and Mössbauer Spectroscopy techniques. X-ray diffraction were performed on the samples to understand the structural characteristics and get information about elements and phases present in the powder after different time of milling. The refinement of XRD spectra revealed the complete formation of fcc Ni (Fe) disordered solid solution after 24 h of milling time, the Fe and Ni elemental distributions are closely correlated. With increasing the milling time, the lattice parameter increases and the grains size decreases. The Mössbauer experiments were performed on the powders in order to follow the formation of Ni3Fe compound as a function of milling time. From the adjustment of Mössbauer spectra, we extracted the hyperfine parameters. The evolution of hyperfine magnetic field shows that the magnetic disordered Ni3Fe phase starts to form from 6 h of milling time and grow in intensity with milling time. For the milling time more than 24 h, only the Ni3Fe disordered phase is present with a mean hyperfine magnetic field of about 29.5 T. The interpretation of the Mossbauer spectra confirmed the results obtained by XRD.


2021 ◽  
Author(s):  
Natalia Kazak ◽  
Yurii V. Knyazev ◽  
Vyacheslav Zhandun ◽  
Juan Bartolomé ◽  
Ana Arauzo ◽  
...  

The ludwigite Co2FeBO5 has been studied experimentally using 57Fe Mössbauer spectroscopy and theoretically by means of the DFT+GGA calculations. The room-temperature Mössbauer spectra are composed of four quadrupole doublets corresponding...


Mineralogia ◽  
2013 ◽  
Vol 44 (1-2) ◽  
pp. 3-12 ◽  
Author(s):  
Kamaleldin M. Hassan ◽  
Julius Dekan

AbstractOlivine basalts from southern Egypt were studied by 57Fe Mössbauer spectroscopy at 297 and 77 K, and by optical microscopy and X-ray diffraction. The 57Fe Mössbauer spectra show three-magnetic sextets, three doublets of ferrous (Fe2+), and a weak ferric (Fe3+) doublet that is attributable to a nanophase oxide (npOx). The magnetic sextets relate to titanomagnetite and the Fe2+ doublets to olivine, pyroxene, and ulvöspinel. Variations in the hyperfine parameters of the various Fe components are attributed to changes in the local crystal chemistry. The intensity of oxidation (Fe3+/ΣFe) in the rocks varies from 20-27% with the oxidized iron largely residing in the titanomagnetite.


Clay Minerals ◽  
2002 ◽  
Vol 37 (4) ◽  
pp. 591-606 ◽  
Author(s):  
E. De Grave ◽  
C. A. Barrero ◽  
G. M. Da Costa ◽  
R. E. Vandenberghe ◽  
E. Van San

AbstractThis paper presents various aspects, revealed by Mössbauer spectroscopy, of structural and magnetic properties of Al-substituted small-particle soil-related oxides. For goethite we focus on the relations between the hyperfine fields on the one hand, and crystallinity and Al content on the other. It is argued that these relations only provide a rough estimate of the Al content in natural samples. The ferrimagnetic-like behaviour reflected in the external-field Mössbauer spectra (4.2 K, 60 kOe) of certain Al goethites is presented. The spectra obtained for lepidocrocites are not spectacular, but confirmed that up to ∼10 at.% Al can be incorporated in the structure. Three differently-made series of hematites are considered. The Morin transition and spin structures in hematite are very sensitive to crystallinity and Al content, and probably to the presence of structural OH–. Integral low-energy electron Mössbauer spectroscopy on non-substituted samples indicates that the Morin-transition temperature in the surface layers (2 to 5 nm) is not significantly shifted from the bulk value. Measurements in extremely high magnetic fields (140 kOe) have shown that a spin-flip transition is induced in highly-substituted samples which exhibit no Morin transition in zero field. The use of external fields is crucial for the characterization and precise determination of the hyperfine parameters and site occupancies for maghemites, and for phase analyses of magnetic soils.


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.


1990 ◽  
Vol 68 (2) ◽  
pp. 350-355 ◽  
Author(s):  
D. Y. Gin ◽  
M. S. R. Cader ◽  
J. R. Sams ◽  
F. Aubke

Addition of 1,3,5-trimethylbenzene (mesitylene or mes) to the tin(II) salts, Sn(SO3F)2 and Sn(SbF6)2, results in the formation of adducts of the composition Sn(SO3F)2•mes and Sn(SbF6)2•2mes in very high yield. The adducts are characterized by chemical analysis and infrared spectra. The adduct formation is followed by 119Sn Mössbauer spectroscopy. It appears that only tin(II) compounds with large, weakly nucleophilic anions are capable of forming mesitylene adducts, while SnCl2, SnF2, and stannocene do not give any indication of adduct formation under similar conditions. Keywords: tin(II)–mesitylene complexes, synthesis, vibrational study, 119Mossbauer spectra.


1974 ◽  
Vol 52 (13) ◽  
pp. 2375-2379 ◽  
Author(s):  
Jack G. Ballard ◽  
Thomas Birchall ◽  
John B. Milne ◽  
W. Duncan Moffett

The 121Sb Mössbauer spectra of a number of SbX4− and Sb2X93− salts have been recorded. Only SbF4−, SbCl4−, and Sb2F93− show significantly large quadrupole splittings with the 5s electrons being stereochemically active.


2012 ◽  
Vol 190 ◽  
pp. 455-458 ◽  
Author(s):  
V. M. Cherepanov ◽  
M. A. Chuev ◽  
M. A. Polikarpov ◽  
S. Yu. Shishkov

Film composites based on magnetite Fe3O4 nanoparticles in the polyvinyl alcohol (PVA) matrix and the dried ferrofluid ARA-250 (Chemicell GmbH, Germany) were studied at temperatures 78-300 K by Mössbauer spectroscopy and magnetic measurements in magnetic fields H < 5 kOe. The Mössbauer spectra taken in magnetic fields show essential restoration of the magnetic hyperfine structure characteristic for the nanoparticles. The experimental Mössbauer spectra have been analyzed within the recently developed three-level [ and multi-level [ relaxation models of magnetic dynamics in an ensemble of single-domain particles. These models take into account the precession and diffusion of particles uniform magnetization as well as the particles size distribution and interparticle interactions.


1992 ◽  
Vol 247 ◽  
Author(s):  
H. H. Wei ◽  
Y. F. Chang

ABSTRACTSeveral new examples of ferro- and antiferromagnetic organometallic and coordinated compounds have been investigated by means of the temperature-dependent magnetic measurements and Mössbauer spectroscopy. Above 70 K the Cu3 [Fe(CN)6] 2-4H2O compound is ferromagnetic as it obeys the Curie-Weiss experession, χm= C/(T-θ), with θ = 25 K; μeff evalued at 200 K is 4.91 μβ. Below 20 K this compound displays the onset of spontaneous magnetization in zero applied field. Above 10 K the Cu[(bpy>2] 3 [Fe(CN)6] 2.5H2O is also ferromagnetic (θ= 2.5 K). Above 20 K the antiferromagnetic [Fe(C5H4Me)2] + [TCNOJ- (θ= 3.25 K) and [Fe(C5H4Me)2]+[TCNE]- (θ= -3.64 K) obey the Curie-Weiss expression. The e.p.r. and Mössbauer spectra for these compounds have been discussed.


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