Relevant bibliographies by topics / Mossbauer

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  2. Dissertations / Theses
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  4. Book chapters
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Academic literature on the topic 'Mossbauer'

Author: Grafiati
Published: 4 June 2021
Last updated: 31 January 2023

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Journal articles on the topic "Mossbauer"

1

Kamzin A. S., Obaidat I. M., Semenov V. G., Narayanaswamy V., Al-Omari I. A., Issa B., and Buryanenko I. V. "Structure and properties of Co-=SUB=-x-=/SUB=-Mn-=SUB=-1-x-=/SUB=-Fe-=SUB=-2-=/SUB=-O-=SUB=-4-=/SUB=- nanoparticles depending on the amount of Co ions (0≤ x≤ 1.0)." Physics of the Solid State 64, no. 6 (2022): 714. http://dx.doi.org/10.21883/pss.2022.06.53838.298.

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The properties of magnetic nanoparticles (MNPs) of spinel ferrites CoxMn1-xFe2O4 (at x=0.0; 0.2; 0.3; 0.4; 0.5; 0.6; 0.8; 1.0) synthesized by chemical co-precipitation method have been studied. The studies of the synthesized CoxMn1-xFe2O4 MNPs were carried out using X-ray diffraction (XRD), Raman scattering and Mossbauer spectroscopy. The results of XRD, Raman and Mossbaur studies indicate that the obtained CoxMn1-xFe2O4 MNPs are single-phase. It was established from XRD measurements that the average size of CoxMn1-xFe2O4 crystallites is 34.86 nm for MnFe2O4 (x=0) and decreases to 14.99 nm for CoFe2O4 (x=1.0) with increasing Co ions concentration. An analysis of the Mossbaur spectra showed that the average crystallite size varies from 25 nm for MnFe2O4 (x=0) to 12 nm for CoFe2O4 (x=1.0). On the Raman spectra of CoxMn1-xFe2O4 MNPs, in the region of ~620 cm-1, splitting of the A1g line is observed, which means that the studied MNPs have a reverse spinel structure. The intensity ratio of the A1g (1) and A1g (2) peaks indicates a significant redistribution of the Co2+ and Fe3+ cations between tetra- and octahedralpositions in MNPs of the CoxMn1-xFe2O4 ferrite, which is confirmed by Mossbauer data. Mossbaur spectroscopy data indicate that the synthesized CoxMn1-xFe2O4 MNPs consist of large particles with magnetic ordering and small particles in the paramagnetic phase. With an increase in the concentration of Mn ions, the proportion of fine particles increases, which leads to a decrease in the magnetic blocking temperature. The saturation magnetization of MNPs at x=0.2 (Co0.2Mn0.8Fe2O4) is 57.41 emu/g and this sample, as was found in [V. Narayanaswamy, I.A. Al-Omari, A.S. Kamzin, B. Issa, H.O. Tekin, H. Khourshid, H. Kumar, A. Mallya, S. Sambasivam, I.M. Obaidat. Nanomaterials 11, 1231 (2021)] has the highest specific absorption rate. As shown by Mossbauer studies, this is due to the fact that these particles are in a superparamagnetic state and the magnetic blocking temperature of these MNPs is in the region of ~315 K, which is most suitable for the treatment of malignant tumors by magnetic hyperthermia. Thus, the synthesized CoxMn1-xFe2O4 MNPs are promising for biomedical applications. Keywords: spinel ferrites CoxMn1-xFe2O4, magnetic structure, superparamagnetism, Mossbauer spectroscopy, materials for biomedicine.
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Norton, S. J. "Mossbauer imaging." Journal of Research of the National Bureau of Standards 92, no. 5 (September 1987): 325. http://dx.doi.org/10.6028/jres.092.032.

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Adar, F., B. Lenain, D. C. Cook, and S. J. Oh. "Corrosion Product Identification by Micro-Raman and Mossbauer Spectroscopy." Microscopy and Microanalysis 4, S2 (July 1998): 506–7. http://dx.doi.org/10.1017/s1431927600022650.

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Micro-Raman spectrometry and Mossbauer spectroscopy have been used to identify the corrosion products on a steel coupon exposed in an industrial environment for 16 years. The Raman analysis was performed on a polished metallographic cross-section in order to map the oxides across the thickness of the coating. The spectra were recorded using a LabRam Micro-Raman spectrograph incorporating a 17 mW HeNe laser (attenuated to 1 mW to prevent oxide transformation), focused to 1 μm spot size, and 1800 g/mm grating. The confocal line-scan imaging enabled 100 spectra to be recorded in one scan at 0.5 um intervals across the thickness of the coating. The Mossbauer analysis was performed using in-situ scattering Mossbauer spectroscopy on the attached corrosion coating and transmission Mossbauer spectroscopy at 300K and 77K on the removed coating, to measure the fraction of each oxide present. Micro-Raman spectrometry showed that the corrosion products had formed in distinct layers as shown in Figure 1.
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Tulebayeva, Dinara, Assel Yermekova, Artem Kozlovskiy, and Maxim Zdorovets. "Investigation of phase transformations of iron nanoparticles during thermal annealing." EPJ Web of Conferences 201 (2019): 02003. http://dx.doi.org/10.1051/epjconf/201920102003.

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Structural properties and phase composition of nanoparticles based on iron oxide were studied. Mossbauer spectroscopy, X-ray diffraction, and scanning electron microscopy were used for the analysis of phase transformations. According to XRD and Mossbauer spectroscopy data, an increase in the annealing temperature, as well as the subsequent phase transformations of magnetite into maghemite and then to hematite, indicate an improvement in the structure and a decrease in microdistortions in the lattice as a result of annealing defects and vacancies. According to Mossbauer spectroscopy data at temperatures above 400°C, the lines of characteristic FeO, which are characteristic for disordered iron oxide, are observed, which also confirms the improvement of the crystal structure of nanoparticles.
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Pietrusiewicz, Pawel, Marcin Nabialek, and Bartlomiej Jez. "Structural and Magnetic Relaxation of Fe61Co10Y8Mo1B20 Bulk Amorphous Alloy Obtained Using Two Methods." Revista de Chimie 69, no. 8 (September 15, 2018): 2097–101. http://dx.doi.org/10.37358/rc.18.8.6481.

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Bulk amorphous Fe61Co10Y8Mo1B20 alloys in the form of plates have been prepared using two methods: suction casting and injection casting. The structure of the as cast samples have been studied using Mossbauer spectroscopy. The obtained Mossbauer spectra are typical for materials of amorphous structure. In the hyperfine field distributions obtained from the Mossbauer spectra analysis, there are variations between the probability of occurrence of magnetic atoms around central atom. Then, magnetic susceptibility disaccommodation has been measured for the tested samples. These measurements indicate that the structural relaxation in the studied samples occur at the elementary level. Injection casting method for the tested alloy determines, in the material volume, the formation of more point relaxators in the form of free volume.
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Al-Alawi, Z., A. M. Gismelseed, A. A. Yousif, M. A. Worthing, H. H. Sutherland, A. M. Rais, M. E. El-Zain, and A. D. Al-Rawas. "Cation Distribution in Natural Chromites from Oman." Sultan Qaboos University Journal for Science [SQUJS] 1, no. 1 (January 1, 1996): 55. http://dx.doi.org/10.24200/squjs.vol1iss1pp55-61.

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Two specimens or natural chromite from the Oman ophiolite were studied using Mossbauer Spectroscopy (MS), X-ray Diffraction (XRD). and Scanning Electron Microscopy (SEM). The diffraction patterns obtained at room temperature showed that the two specimens have a face-centered cubic spinal structure. Their Mossbauer spectra at 295 K. 160 K and 78 K have been fitted to three doublets. assigned to two Fe 2+ at the tetrahedral (A1+,A2) sites and one Fe1+ at the octahedral (B) site. The ferrous-ferric ratio obtained from the Mossbauer analysis together with the atomic concentration derived from the microprobe data are used to derive the chemical formulae for the two specimens. The data also supports also supports a model of ordered caution distribution in the specimens examined.
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Tomov, T., S. Asenov, B. Kunov, and I. Spirov. "A Mossbauer source thermostat." Measurement Science and Technology 6, no. 12 (December 1, 1995): 1717–20. http://dx.doi.org/10.1088/0957-0233/6/12/010.

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Fruchart, R., P. L'Heritier, P. Dalmas de Reotier, D. Fruchart, P. Wolfers, J. M. D. Coey, L. P. Ferreira, R. Guillen, P. Vulliet, and A. Yaouanc. "Mossbauer spectroscopy of R2Fe14B." Journal of Physics F: Metal Physics 17, no. 2 (February 1987): 483–501. http://dx.doi.org/10.1088/0305-4608/17/2/017.

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Cardile, CM, and DG Lewis. "Mossbauer spectroscopic evidence of a IVFe3+ intermediate in the oxidation of Fe(Oh)2 to α-FeOOH." Soil Research 29, no. 3 (1991): 399. http://dx.doi.org/10.1071/sr9910399.

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Mossbauer spectroscopy was used to study the oxidation of Fe(OH)2 under high pH conditions with the aim of detecting the formation of Fe(OH)3. The Mossbauer spectral parameters indicated that a small IVFe3+ component was initially present in the Fe(OH)2. The Mossbauer spectra were recorded at 77 K, thus any Fe species in solution would also be observed in the frozen state. The small IVFe3+ component increased progressively with the oxidation of the Fe(OH)2, maximizing with the onset of �-FeOOH formation. As �-FeOOH formation increased, the IVFe3+ component decreased, with �-FeOOH being the final sole phase. It is suggested that the Mossbauer spectral parameters indicate that a component such as Fe(OH)2 may form at high pH values as used in this study. Furthermore, any Fe3+ produced by the initial oxidation of Fe(OH)2 is exsolved from the solid and at the high pH of the surrounding liquid produces Fe(OH)-4 until the formation of the more stable �-FeOOH begins. This suggests Fe(OH)2 could be the building blocks for �-FeOOH in alkaline solution. No apparent Fe(OH)3 phase was observed as anticipated.
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Pavlenko A.V., Stryukov D. V., and Kubrin S.P. "The phase composition and structure of the BiFeO-=SUB=-3-=/SUB=- film grown on MgO(001) substrate by high frequency cathode deposition in oxygen atmosphere." Physics of the Solid State 64, no. 2 (2022): 206. http://dx.doi.org/10.21883/pss.2022.02.52969.215.

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The crystal structure and Mossbauer spectroscopy studies results for BiFeO3 film growth on the MgO(001) single crystal substrate are present in the paper. It been shown that film have high crystal perfection and low defectiveness which results in appearing of narrow lines during the theta-2theta and φ scanning and the small (lower than 0.7o) disorientation of film and substrate crystal axes. It is been revealed that unit cell of BiFeO3/MgO(001) heterostructure possess monoclinic symmetry and deformation of unit cell is negligible. The Mossbauer study shows that magnetic subsystem of film has spatial spin-modulated structure with zero value of anharmonicity parameter (m). This indicate that at room temperature the magnetic anisotropy changes from the "easy axis" type to "easy plane" type. Keywords: thin films, bismuth ferrite, Mossbauer effect.
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Dissertations / Theses on the topic "Mossbauer"

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Cowie, Bruce C. C. "Novel applications of Mossbauer spectroscopy." Thesis, Heriot-Watt University, 1988. http://hdl.handle.net/10399/934.

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Sheen, Nicholas I. "Mossbauer spectroscopy of linear chain systems." Thesis, University of Canterbury. Physics, 1994. http://hdl.handle.net/10092/8074.

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Since the prediction by Villain in 1975 of moving magnetic domain walls (or solitons) in 1-dimensional Ising-like antiferromagnets, there has been interest in compounds with these properties. Mössbauer spectra of CsCo₀⁠⁡⁢⁣⁤.₉₉Fe₀.₀₁Cl₃ in the magnetically ordered phases below TN₁ = 21.2 K were analysed by Ward et al (1987) assuming that only the two lowest energy electronic states of the ⁵⁷Fe⁲⁺ ion were significantly occupied (the 2-level relaxation model). This assumption is unreliable above approximately 18 K because it was estimated that the third lowest-lying electronic state of Fe⁲⁺ was significantly occupied at those temperatures. Nevertheless, it was found that two relaxation processes were present, one attributed to moving domain walls, and the other to transitions between the low-lying electronic states of the Fe⁲⁺ ion. In this work the 2-level relaxation model was extended to include the third lowest-lying electronic state of the Fe⁲⁺ ion. A further extension, the combined relaxation model, enables Mössbauer spectra to be fitted when both 3-level electronic relaxation and relaxation due to moving domain walls occur with similar rates at the same ⁵⁷Fe⁲⁺ site. The quasi 1-dimensional Ising-like antiferromagnetic salt NH₄CₒCl₃ doped with less than 1 atomic % ⁵⁷Fe⁲⁺ was synthesised, and Mössbauer spectra were taken at temperatures between 1.3 and 250 K. The Mössbauer spectra of both CₛC₀₁₋ₓFeₓCl₃ and NHâ‚„Coâ‚ -â‚“Feâ‚“Cl3 in the magnetically ordered phases were analysed using the 2-level, 3-level and combined relaxation models. Although good fits to the Mössbauer spectra of CₛC₀₁₋ₓFeₓCl₃ and NH₄FeₓCl₃ were obtained using all the relaxation models, the combined relaxation model was the most satisfactory since the assumptions of this model were not invalidated by the parameters obtained from the fits. The soliton relaxation rates obtained were much slower than those predicted theoretically and found from other experiments on CsCoCl3. One reason for this which is examined in this thesis is that the determined rates are unduly affected by the approximations made in the relaxation models. Another possible explanation of the discrepancy is that the presence of iron in the cobalt chains changes the soliton dynamics. In order to study the effect of doping NNH₄FeₓCl₃with Fe⁲⁺, the isomorphous crystal NH₄FeₓCl₃ was grown. The magnetic structure of NH₄FeₓCl₃ is expected to be governed by ferromagnetic intra-chain interactions and weaker antiferromagnetic inter-chain interactions. The linewidth broadening of the Mössbauer spectra of NH₄FeₓCl₃ at temperatures up to 10 K is evidence for the existence of magnetic correlations above the Neel temperature (1.7 K). The 4.2 and 1.3 K spectra show that a distribution of magnetic hyperfine fields B are present, possibly due to incommensurate magnetic ordering. At 4.2 K the main components of the Mössbauer spectrum are approximately 79 % with B = 0 and 21 % with B = 5.32 T. At 1.3 K the main components of the Mössbauer spectrum are approximately 72 % with B = 5.2 T and 28 %with B = 0. The non-magnetic subspectrum at 1.3 K may be caused by cancellation between the different components of the magnetic hyperfine field.
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Thorpe, Stephen C. "Surface corrosion studies by Mossbauer spectroscopy." Thesis, Sheffield Hallam University, 1987. http://shura.shu.ac.uk/20440/.

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Transmission [57]Fe Mossbauer Spectroscopy has been used to investigate two standard iron oxides and two environmental corrosion products in the temperature range 10-300 Kelvin. This was achieved using a specially developed Air Products cryogenic refrigeration system using gaseous helium as the refrigerant - thereby removing the requirement of an expensive liquid helium facility normally required for low temperature work. Characteristic spectra and transitions were observed for both the standard oxides. The environmental corrosion products demonstrated the differences in observed spectra between a sample which exhibits only bulk properties and one in which the particle size distribution within the sample is such that relaxation phenomena become important. The interpretations-made from the variable temperature Mossbauer data were confirmed by the complementary technique of X-ray diffraction. Conversion electron Mossbauer spectroscopy (C.E.M.S.) and conversion X-ray Mossbauer spectroscopy (C.X.M.S.) backscatter techniques have also been developed and are now routinely available in our laboratory. The greater escape depth of the conversion X-ray allows the C.X.M.S. method to be used to record spectra from samples to which a protective layer such as a paint, varnish, grease or oil layer has been applied. To ensure a surface sensitive signal, the substrate surfaces had to be enriched in the Mossbauer isotope 57Fe. This was achieved by vacuum evaporation of 57Fe onto the substrate surface and subsequent diffusion of the 57Fe into the near surface region - this diffusion had to be accomplished without oxidising the surface. Samples thus prepared were subsequently exposed to aggressive atmospheres and their CXM spectra recorded. The limitation of the method is that only room temperature spectra can be recorded at present and difficulties are encountered in the assignment of spectra that contain only quadrupole doublets.
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Lukas, B. "Mossbauer studies on iron protoporphyrin 9 complexes." Thesis, University of Essex, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.355388.

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Smith, Roger. "A Mossbauer study of chromite-magnesia refractories." Thesis, Sheffield Hallam University, 1994. http://shura.shu.ac.uk/20372/.

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A range of natural chrome ores, containing iron in two valence states, have been investigated using the technique of Mossbauer spectroscopy. The instrumentation required to cry out the technique was studied and an additional item of equipment was designed and constructed to extend the temperature range over which the effect could be observed. All the chrome ores yielded a complex spectra which could be attributed to a combination of octahedrally and tetrahedrally co-ordinated Fe2+ and Fe3+ quadrupole doublets. A model for fitting the spectra was devised assuming the presence of octahedrally co-ordinated Fe3+ and tetrahedrally co-ordinated Fe2+. The inhomogeneous nature of the samples caused a broadening of the tetrahedral Fe2+ contribution which was fitted as a distribution of three doublets. The Mossbauer parameters obtained were compared with those of pure compounds of a similar structure. Spectra recorded from 12K to 600K enabled effective Debye temperatures to be calculated. Second order Doppler shift (S.O.D.S.) calculations gave values for theta[D] of 385K and 658K for the Fe2+ and Fe3+ contributions respectively. Absorption area data gave similar values. An examination of the temperature dependence of the quadrupole splitting of the Fe2+ contributions appeared to confirm the validity of the proposed fitting model. Estimations of the Fe2+ / Fe3+ ratio were made using the data obtained and yielded values of 1.6 - 3.6.
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Al-Rawwas, Ahmed Dhofar. "A Mossbauer spectroscopy study of strontium iron oxides." Thesis, University of Liverpool, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.385228.

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Houlton, Andrew. "Mossbauer spectroscopic studies of iron(II) sandwich compounds." Thesis, University of Essex, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.252634.

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Abrahams, I. "Mossbauer spectroscopic and structural studies of tin materials." Thesis, City University London, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.375839.

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Cerón, Loayza María Luisa. "Estudio mineralógico de suelos agrícolas por espectroscopía Mossbauer." Bachelor's thesis, Universidad Nacional Mayor de San Marcos, 2001. https://hdl.handle.net/20.500.12672/1505.

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Este trabajo tiene como objetivo determinar los componentes mineralógicos de perfiles de suelos agrícolas con muestras tomadas a diferentes profundidades: superficie, 50 cm y 100 cm, considerando las diferentes fracciones granulométricas de cada muestra, sobre la base de su estructura cristalina y de los parámetros hiperfinos asociados a sitios estructurales ocupados por átomos de hierro (Fe). Las muestras se recolectaron de la zona de Chinchero, Cusco. Las técnicas analíticas utilizadas en este estudio son la difracción de rayos-X (DR-X) y la espectroscopía Mössbauer por transmisión (TMS); como técnicas complementarias se utiliza tratamientos químicos de disolución selectiva de Fe y la microscopía metalográfica. Mediante la TMS se pudo obtener información en forma selectiva de minerales de Fe, ya sean cristalinos o amorfos, y/o de minerales con sustituciones de cationes por Fe. Esta técnica permitió detectar los compuestos de Fe presentes en concentraciones muy bajas y sin importar la presencia de otros compuestos. La alteración de los parámetros Mössbauer da cuenta de la baja cristalinidad y/o sustituciones de los cationes de Fe de los minerales por otros cationes. Esta información se complementa con la que proporcionan DR-X y microscopía metalográfica. Los resultados de las muestras fotografiadas mediante el microscopio metalográfico nos sirve para observar de acuerdo a su coloración la presencia de los componentes mineralógicos, ya se cuarzo, feldespato, plagioclasa, arcillas y óxidos. Los resultados obtenidos nos permiten determinar en forma cualitativa la composición mineralógica de las distintas fracciones granulométricas a diferentes profundidades en los perfiles estudiados. Los resultados por DR-X permiten identificar minerales presentes en alta concentración y cristalinidad de acuerdo a la intensidad de sus picos de difracción; los resultados por EM finalmente nos permiten determinar los compuestos mineralógicos que contienen Fe; algunos de ellos que por su baja concentración y baja cristalinidad no son perceptibles por DR-X. Merece mencionar que en algunos casos fue necesario tomar medidas por TMS enfriando la muestra a temperatura de nitrógeno líquido y helio líquido para discernir el efecto de superparamagnetismo en minerales en forma de granos muy pequeños. Los minerales identificados por DR-X fueron: cuarzo, feldespato potásicos como Sanidine, microline y ortoclasa, minerales de Fe como: hematita, goetita, minerales arcillosos como: illita montmorillonita y muscovita, y la presencia de la calcita. Los minerales identificados por TMS fueron: Minerales de Fe como: hematita, goethita, magnetita, ferrihidrita, y minerales arcillosos como: illita, montmorillonita y muscovita.
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Younis, Adbelhamid Mohamed. "Characterisation of iron in Libyan soil using Mossbauer spectroscopy." Thesis, University of St Andrews, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.731715.

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Books on the topic "Mossbauer"

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Cook, Desmond C. Industrial Applications of the Mössbauer Effect: Proceedings of ISIAME 2000 held in Virginia Beach, USA, 13-18 August 2000. Dordrecht: Springer Netherlands, 2003.

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Marcel, Miglierini, Petridis Dimitris, and North Atlantic Treaty Organization. Scientific Affairs Division., eds. Mossbauer spectroscopy in materials science. Dordrecht: Kluwer, 1999.

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Jones, Stuart Leigh. Mossbauer studies of iron associated with montmorillonite clays. Birmingham: University of Birmingham, 1985.

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V, Morris Richard, and United States. National Aeronautics and Space Administration., eds. Mossbauer mineralogy on the moon: The lunar regolith. [Washington, DC: National Aeronautics and Space Administration, 1997.

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E, Dickson Dominic P., and Berry Frank J. 1947-, eds. Mössbauer spectroscopy. Cambridge: Cambridge University Press, 1986.

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E, Cranshaw T., ed. Mössbauer spectroscopy and its applications. Cambridge [Cambridgeshire]: Cambridge University Press, 1985.

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Maddock, A. G. Mössbauer spectroscopy: Principles and applications. Chichester: Horwood, 1997.

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Pszczoła, Jarosław. Ferrimagnetism and hyperfine interactions of the Dyx̳Fey̳ compounds, their pseudobinaries, and other intermetallics. Cracow: Stanisław Staszic Academy of Mining and Metallurgy, 1987.

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Seeheim Workshop on Mössbauer Spectroscopy (5th 2002). Mössbauer spectroscopy. Dordrecht: Kluwer Academic Publishers, 2003.

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Mitra, S. Applied Mossbauer Spectroscopy. Elsevier Science Pub Co, 1993.

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Book chapters on the topic "Mossbauer"

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Hawthorne, Frank C. "Chapter 8. MOSSBAUER SPECTROSCOPY." In Spectroscopic Methods in Mineralogy and Geology, edited by Frank C. Hawthorne, 255–340. Berlin, Boston: De Gruyter, 1988. http://dx.doi.org/10.1515/9781501508974-010.

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Dunham, W. R., W. R. Hagen, A. Braaksma, H. Haaker, S. Gheller, W. E. Newton, and B. Smith. "Mossbauer and EPR Studies on Nitrogenase." In Nitrogen fixation research progress, 591–96. Dordrecht: Springer Netherlands, 1985. http://dx.doi.org/10.1007/978-94-009-5175-4_81.

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Gel’berg, A. "Angular Correlation in the Mossbauer Effect." In Proceedings of the Dubna Conference on the Mössbauer Effect 1963, 152–54. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-4848-9_15.

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Gol’danskii, V. I. "Applications of the Mossbauer Effect in Chemistry." In Proceedings of the Dubna Conference on the Mössbauer Effect 1963, 177–233. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-4848-9_17.

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DeMarco, M., G. Trbovich, X. Wang, P. G. Mattocks, and M. Naughton. "Mossbauer Effect Studies in YBa2Cu3−YSnYO7−x." In Superconductivity and Applications, 419–24. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4684-7565-4_39.

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Williamson, D. L., B. Morosin, E. L. Venturini, and R. A. Graham. "Mossbauer Study of Shock-Synthesized Zinc Ferrite." In Shock Waves in Condensed Matter, 809–14. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4613-2207-8_119.

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Gol’danskii, R. I., G. M. Gorodinskii, L. A. Korytko, L. M. Krizhanskii, E. F. Makarov, I. P. Suzdalev, and V. V. Khrapov. "Investigation of the Mossbauer Effect in Tin Compounds." In Proceedings of the Dubna Conference on the Mössbauer Effect 1963, 261–68. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-4848-9_23.

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Smorodinskii, Ya. "The Mossbauer Effect and the Theory of Relativity." In Proceedings of the Dubna Conference on the Mössbauer Effect 1963, 87–95. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-4848-9_8.

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Turta, C., Svetlana A. Bobcova, and V. Mereacre. "Mossbauer Spectra of Two Ancient Ceramic Products from Moldova." In Molecular and Structural Archaeology: Cosmetic and Therapeutic Chemicals, 119–22. Dordrecht: Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-010-0193-9_11.

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Alfimenkov, V. P., and Yu M. Ostanevich. "Methods and Compilation of Data on Mossbauer γ-Transitions." In Proceedings of the Dubna Conference on the Mössbauer Effect 1963, 1–15. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-4848-9_1.

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Conference papers on the topic "Mossbauer"

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Bachurin, V. I., I. N. Zakharova, M. A. Shipilin, and A. M. Shipilin. "Mossbauer study of nanomagnetics." In International Conference on Micro- and Nano-Electronics 2009, edited by Kamil A. Valiev and Alexander A. Orlikovsky. SPIE, 2009. http://dx.doi.org/10.1117/12.854768.

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Yadav, Ravi Kumar, R. Govindaraj, and G. Amarendra. "Mossbauer spectroscopic studies in ferroboron." In DAE SOLID STATE PHYSICS SYMPOSIUM 2016. Author(s), 2017. http://dx.doi.org/10.1063/1.4980202.

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Bibicu, I., G. Nicolescu, and C. Cretu. "Mossbauer backscattering measurements on Sn." In Advanced Topics in Optoelectronics, Microelectronics, and Nanotechnologies IV, edited by Paul Schiopu, Cornel Panait, George Caruntu, and Adrian Manea. SPIE, 2009. http://dx.doi.org/10.1117/12.823676.

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Singh, L. Herojit, R. Govindaraj, S. Ravishankar, S. Rajagopalan, and G. Amarendra. "Mossbauer spectroscopic studies on NiCoFe." In NANOFORUM 2014. AIP Publishing LLC, 2015. http://dx.doi.org/10.1063/1.4918240.

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Taylor, R. Dean, and Gilbert R. Hoy. "Mossbauer Effect Experiments Applicable To Grasers." In 1988 Los Angeles Symposium--O-E/LASE '88, edited by Randy C. Jones. SPIE, 1988. http://dx.doi.org/10.1117/12.943893.

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Kitaol, S., T. Matsuyama, M. Seto, Y. Maeda, S. Masubuchi, and S. Kazama. "Mossbauer study of polythiophene and its derivatives." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.834692.

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Hamdeh, H. H., and S. A. Oliver. "Mossbauer Characterization Of Non-Equlilibrium Zinc Ferrites." In 1997 IEEE International Magnetics Conference (INTERMAG'97). IEEE, 1997. http://dx.doi.org/10.1109/intmag.1997.597703.

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Pathak, Biswajit, and Bosanta R. Boruah. "Zonal wavefront estimation using an array of hexagonal grating patterns." In MOSSBAUER SPECTROSCOPY IN MATERIALS SCIENCE - 2014. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4898224.

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Cuda, Jan, Tomas Kohout, Jiri Tucek, Jan Filip, Ondrej Malina, Michal Krizek, and Radek Zboril. "In-field 57Fe Mössbauer spectroscopy below spin-flop transition in powdered troilite (FeS) mineral." In MOSSBAUER SPECTROSCOPY IN MATERIALS SCIENCE - 2014. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4898605.

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Aparicio, Claudia, Jan Filip, Miroslav Mashlan, and Radek Zboril. "The influence of the iron content on the reductive decomposition of A3−xFexAl2Si3O12 garnets (A = Mg, Mn; 0.47 ≤ x ≤ 2.85)." In MOSSBAUER SPECTROSCOPY IN MATERIALS SCIENCE - 2014. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4898606.

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Reports on the topic "Mossbauer"

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Oliver, Frederick W., and Windsor Morgan. Mossbauer Investigation of Intermetallic Hydrides. Fort Belvoir, VA: Defense Technical Information Center, December 1985. http://dx.doi.org/10.21236/ada163762.

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Kocharovskaya, Olga, Zameer Hasan, and James Carroll. Laser Modification of Mossbauer Spectra in Eu2+:CaS. Fort Belvoir, VA: Defense Technical Information Center, August 2001. http://dx.doi.org/10.21236/ada402837.

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Hoy, Gilbert R. SDIO/IST Ultrashort Wavelength. Mossbauer and Gamma-Ray Studies for Grasers. Fort Belvoir, VA: Defense Technical Information Center, June 1994. http://dx.doi.org/10.21236/ada283091.

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Riedel, F. R. Ferrocyanide safety program: FY 1995 report on Mossbauer spectroscopy tank activities. Office of Scientific and Technical Information (OSTI), October 1995. http://dx.doi.org/10.2172/409839.

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G.P. Huffman, K. R. P. M. Rao, and F.E. Huggins. MOSSBAUER SPECTROSCOPY STUDIES OF IRON CATALYSTS USED IN SLURRY PHASE FISCHER-TROPSCH SYNTHESIS. Office of Scientific and Technical Information (OSTI), February 1998. http://dx.doi.org/10.2172/769337.

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Hoy, Gilbert R. SDIO/IST Ultrashort Wavelength Laser: Novel Experimental Schemes for Observing the Mossbauer Effect in Long-Lived Nuclear Levels and Nuclear Coherent States. Fort Belvoir, VA: Defense Technical Information Center, March 1989. http://dx.doi.org/10.21236/ada207838.

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Multi-beam Mossbauer scattering facility. Final technical report. Office of Scientific and Technical Information (OSTI), October 1994. http://dx.doi.org/10.2172/10195852.

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