Constrained growth of anisotropic magnetic δ-FeOOH nanoparticles in the presence of humic substances

    Function distribution magnetic splitting the mossbauer spectrum for different temperatures of the composite d-FeOOH-HSConstrained growth of anisotropic magnetic δ-FeOOH nanoparticles in the presence of humic substances. Polyakov A.Yu., Goldt A.E., Sorkina T.A., Perminova I.V., Pankratov D.A., Goodilin E.A., Tretyakov Y.D. //CrystEngComm. 2012. V.14. №23. P.8097-8102.Search the full text below. Ищи полный текст ниже.

    Natural polyelectrolytes, humic substances, are suggested to control in situ growth of feroxyhyte nanoparticles of a highly reduced mean size and with enhanced colloidal stability in salt solutions. The feroxyhyte is formed as 2-5 nm thick and 20 × 20 nm wide nanoflakes due to the blocking of developing facets of feroxyhyte and constraints caused by diffusion limitations of ionic constituents across partially charged branches of humic substances.

    Superparamagnetic iron oxide nanoparticles (SPIONs) are known as effective biocompatible agents for various biomedical applications like drug delivery, in vivo magnetic resonance imaging, cell and protein separation, hyperthermia and transfection. At present, synthesis and application of rods, disks, fibers, tubes, sheets, ellipsoids, dumbbell-shaped, acorn-shaped and other anisotropic nanoparticles attract growing attention because of their unique properties. Aggregation is a serious problem in the preparation and storage of such magnetic nanoparticles limiting considerably their practical applications. This problem can be solved by a surface modification of nanoparticles with organic macromolecules, their preparation in the presence of surfactants, application of hydrophilic, surface-active ligands improving biocompatibility and resulting in multifunctional nanoparticles for medical diagnostics.

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    Possibilities of cryogenic autoradiography

    Characteristic curves obtained under different conditions: 1, at room temperature; 2, at the temperature of liquid nitrogen (experimental data, approximating straight lines of the regions of normal exposures, regions of photographic latitude, and inertia points are shown).

    Possibilities of cryogenic autoradiography. Pankratov D.A., Korobkov V.I. //Journal of Analytical Chemistry. 2014. V. 69. Is. 7. P. 632–637Search the full text below. Ищи полный текст ниже.

    Photographic properties of the nuclear photographic detector BioMax MR Film from KODAK are studied at the temperature of liquid nitrogen. The characteristic curves obtained at room and cryogenic temperatures indicate that the detector retains its physical and photographic properties, and its possibilities can be expanded to studies of deeply frozen samples. The data obtained point to an increase in the sensitivity of the photographic material frozen to cryogenic temperatures at short exposures.

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    Synthesis and magnetic properties of cobalt ferrite nanoparticles in polycarbosilane ceramic matrix

    Mössbauer spectra of the sample comprised of cobalt ferrite nanoparticles in a ceramic matrix after sintering in argon.Synthesis and magnetic properties of cobalt ferrite nanoparticles in polycarbosilane ceramic matrix. Yurkov G.Y., Shashkeev K.A., Kondrashov S.V., Popkov O.V., Shcherbakova G.I., Zhigalov D.V., Pankratov D.A., Ovchenkov E.A., Koksharov Yu.A. //Journal of Alloys and Compounds. 2016. V.686. P.421–430

    Composite materials comprised of a ceramic matrix with metal-containing nanoparticles were prepared by sintering a blend of cobalt ferrite nanoparticles and polycarbosilane. Sintering process was performed either in air or argon, resulting in different material composition. The air-sintering materials consist mainly of oxide phases (silica matrix and cobalt ferrite nanoparticles). The process of sintering in argon leads to partial reduction of oxides and formation of α-Fe, carbide and silicate phases. The prepared samples were characterized by the SEM, TEM, XRD and EMR techniques and the Mössbauer spectroscopy. Static magnetic properties were also studied. All samples were found to be soft magnetic. Sintering, especially in argon, increases remnant magnetization of resulting composite products.

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    Mössbauer study of oxo derivatives of iron in the Fe2O3-Na2O2 system

    Possible models for describing of sum Mössbauer spectra at different temperaturesMössbauer study of oxo derivatives of iron in the Fe2O3-Na2O2 system. Pankratov D.A. //Inorganic Materials. 2014. V. 50. № 1. P. 82-89Search the full text below. Ищи полный текст ниже.

    Various compositions of oxo derivatives of iron reacting with sodium peroxide have been studied by Mössbauer spectroscopy. We have examined several mathematical models of the measured spectra. The results obtained are inconsistent with hypotheses made previously that such conditions may lead to the formation of compounds of iron in oxidation states above (+6). We demonstrate that a large excess of an alkali peroxide leads, most likely, to the formation of at least two iron(V) derivatives in tetrahedral coordination. In their Mössbauer spectra, they have isomer shifts of −0.45 and −0.51 mm/s and unusually large quadrupole splittings: 1.32 and 1.94 mm/s (at room temperature).

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    Potassium hexahydroperoxostannate: synthesis and structure

    Mossbauer spectra of (1) K2Sn(OH)6 and (2) K2Sn(00H)6
    Potassium hexahydroperoxostannate: synthesis and structure.
     Ippolitov E.G., Tripol'skaya T.A., Prikhodchenko P.V., Pankratov D.A.
    //Russian Journal of Inorganic Chemistry. 2001. V.46. №6. P.851-857 Search the full text below. Ищи полный текст ниже.

    Polycrystalline potassium hexahydroperoxostannate was prepared by replacement of hydroxo groups in potassium hexahydroxostannate upon its dissolution in hydrogen peroxide. A comparative study of the product and the starting hydroxostannate by powder X-ray diffraction analysis, thermogravimetry, and IR, 2H, 39K, and 119Sn NMR, and Mössbauer spectroscopy was carried out. The peroxo compound K2Sn(OOH)6 crystallizes in the hexagonal system with a = 7.264(7) Å, c = 10.168(4) Å. IR, NMR, and Mössbauer spectroscopy data show that the tin coordination polyhedron in the peroxo compound is an octahedron formed by the coordinated hydroperoxo groups.

    Previously, sodium hexahydroperoxostannate was prepared and characterized by powder X-ray diffraction analysis, thermogravimetry, IR, 1H NMR, and Mossbauer spectroscopy, and by thermodynamic and kinetic method. The tin atom in this compound were found to occur in the octahedral environment of hydroperoxo group. It appeared pertinent to confirm the possibility of formation of this type of tin compound by preparing a new hydroperoxo complex. To this end, we performed the first synthesis of potassium hexahydroperoxostannate. Comparative study of potassium hexahydrosstannate (1) and hexahydroperoxosstannate (2) and their deuterated analogue (1a and 2a, respectively) was carried out by powder X-ray diffraction analysis, thermogravimetry, and IR, NMR (2H, 39K and 119Sn), and Mossbauer spectroscopy.

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