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Raman spectra of diphenylalanine microtubes: polarisation and temperature effects / A. Krylov, S. Krylova, S. Kopyl [et al.] // Crystals. - 2020. - Vol. 10, Is. 3. - Ст. 224, DOI 10.3390/cryst10030224. - Cited References: 43. - This research was funded by the Russian Foundation for Basic Research grant number 18-02-00754, F.S. thanks Scientific and Technological Research Council of Turkey for support under Grant Number 115F227. S.Kopyl and A.Kholkin thank the joint project Portugal-Turkey TUBITAK/0006/2014. This work was developed within the scope of the project CICECO-Aveiro Institute of Materials, refs. UIDB/50011/2020 & UIDP/50011/2020, financed by national funds through the FCT/MEC. S.Kopyl, P.Z. and A.Kholkin were partly supported by FCT (Portugal) through the project "BioPiezo"-PTDC/CTM-CTM/31679/2017 (CENTRO-01-0145-FEDER-031679). Part of this work was funded by national funds (OE), through FCT-Fundacao para a Ciencia e a Tecnologia, I.P., in the scope of the framework contract foreseen in the numbers 4, 5, and 6 of the article 23, of the Decree-Law 57/2016, of 29 August, changed by Law 57/2017, of 19 July. . - ISSN 2073-4352

РУБ Crystallography + Materials Science, Multidisciplinary
Рубрики:
PIEZOELECTRIC PROPERTIES
   PHASE-TRANSITIONS
   SPECTROSCOPY
   SCATTERING
Кл.слова (ненормированные):
diphenylalanine -- Raman spectra -- phase transition -- polarisation -- temperature effects
Аннотация: Diphenylalanine microtubes have remarkable physical properties that allow one to use them in electronics. In this work, we measured polarised temperature-dependent Raman spectra in self-assembled diphenylalanine microtubes grown from the solution. We observed the anomalous temperature behaviour of the Raman lines. Their temperature changes were minimal, which required a significant improvement in the resolution and stability of Raman measurements. The anomalies in the behaviour of the spectra at about 178 K, 235 K, 255 K, 278 K, 296 K, 398 K and 412 K were observed. The structural phase transition at 398 K is irreversible. This transition is associated with the release of water molecules from nanochannels. The irreversible phase transition has a temperature range of about 10 K.

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Держатели документа:
Res Ctr KSC SB RAS, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.
Univ Aveiro, Dept Phys, P-3810193 Aveiro, Portugal.
Univ Aveiro, CICECO Mat Inst Aveiro, P-3810193 Aveiro, Portugal.
Moscow Inst Phys & Technol, Dolgoprudnyi 141700, Russia.
Istanbul Tech Univ, Dept Phys Engn, TR-34469 Istanbul, Turkey.
Ural Fed Univ, Inst Nat Sci & Math, Ekaterinburg 620026, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.

Доп.точки доступа:
Krylov, A. S.; Крылов, Александр Сергеевич; Krylova, S. N.; Крылова, Светлана Николаевна; Kopyl, Svitlana; Salehli, Ferid; Zelenovskiy, Pavel; Vtyurin, A. N.; Втюрин, Александр Николаевич; Kholkin, Andrei; Russian Foundation for Basic ResearchRussian Foundation for Basic Research (RFBR) [18-02-00754]; Scientific and Technological Research Council of TurkeyTurkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) [115F227]; project Portugal-Turkey [TUBITAK/0006/2014]; FCT/MEC [UIDB/50011/2020, UIDP/50011/2020]; FCT (Portugal) through the project "BioPiezo" [PTDC/CTM-CTM/31679/2017 (CENTRO-01-0145-FEDER-031679)]; national funds (OE), through FCT-Fundacao para a Ciencia e a Tecnologia, I.P.
}
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Effect of calcination temperature on activity of Fe2O3-Al2O3 nanocomposite catalysts in CO oxidation / A. M. Kremneva, A. V. Fedorov, O. A. Bulavchenko [et al.] // Catal. Lett. - 2020. - Vol. 150. - P. 3377-3385, DOI 10.1007/s10562-020-03250-8. - Cited References: 31. - This work was supported by the Russian Science Foundation (Grant No. 17-73-20157). The experiments were performed using facilities of the shared research center "National center of investigation of catalysts" at Boreskov Institute of Catalysis. The authors thank A.Yu. Gladky for the TPR measurements and Z.S. Vinokurov for the XRD measurements. . - ISSN 1011-372X. - ISSN 1572-879X

РУБ Chemistry, Physical
Рубрики:
MOSSBAUER
   SPECTROSCOPY
   CHEMISTRY
   IRON
   XPS
   ADSORPTION
   OXYGEN
   FE
Кл.слова (ненормированные):
Environmental catalysis -- Nanostructure -- Gasification -- Oxidation -- Mossbauer spectroscopy
Аннотация: Nanocomposite Fe–Al oxide catalysts were prepared by the melting of iron and aluminum nitrates with the subsequent calcination in air at different temperatures. It was found that the catalysts calcined at 450 °C are more active in the oxidation of CO than the catalysts calcined at 700 °C. X-ray diffraction and X-ray photoelectron spectroscopy showed that all the catalysts consist of hematite, α-Fe2O3 nanoparticles, and Al2O3 in an amorphous state. Iron oxide is the active component, which provides the oxidation of CO, while alumina is a texture promoter. The increase in the calcination temperature leads to a minor increase in the average size of hematite nanoparticles and an insignificant decrease in the specific surface area. Kinetic measurements showed that the oxidation of CO over the Fe–Al catalysts calcined at 450 and 700 °C proceeds with the activation energy of 61–69 and 91 kJ/mol, respectively. This means that the low-temperature and high-temperature catalysts contain different active species. Temperature-programmed reduction with CO indicated that the decrease in the calcination temperature improves the reducibility of the Fe-Al nanocomposites. According to 57Fe Mössbauer spectroscopy, the low-temperature catalysts contain hydrated iron oxides (acagenite and ferrihydrite) and a significant amount of highly defective hematite, which is absent in the high-temperature catalyst. These species can provide the enhanced activity of the low-temperature catalysts in the oxidation of CO.

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Держатели документа:
Boreskov Inst Catalysis, Novosibirsk 630090, Russia.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.

Доп.точки доступа:
Kremneva, A. M.; Fedorov, A. V.; Bulavchenko, O. A.; Knyazev, Yu. V.; Князев, Юрий Владимирович; Saraev, A. A.; Yakovlev, V. A.; Kaichev, V. V.; Russian Science FoundationRussian Science Foundation (RSF) [17-73-20157]; National center of investigation of catalysts" at Boreskov Institute of Catalysis
}
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Core-hole localization and ultra-fast dissociation in SF6 / V. Ekholm, G. S. Chiuzbaian, C. Sathe [et al.] // J. Phys. B. - 2020. - Vol. 53, Is. 18. - Ст. 185101, DOI 10.1088/1361-6455/aba204. - Cited References: 36. - This work was supported by the Swedish Research Council (VR). The calculations were performed on resources provided by the Swedish National Infrastructure for Computing (SNIC). FG acknowledges support within the Russian Science Foundation (Project No. 16-12-10109) . - ISSN 0953-4075. - ISSN 1361-6455

РУБ Optics + Physics, Atomic, Molecular & Chemical
Рубрики:
X-RAY-EMISSION
   SYMMETRY-BREAKING
   AB-INITIO
   SPECTROSCOPY
   SPECTRA
Кл.слова (ненормированные):
SF6 -- resonant inelastic x-ray scattering -- symmetry selection rules -- ultrafast dynamics -- vibronic couplings
Аннотация: Resonant inelastic x-ray scattering spectra excited at the fluorine K resonances of SF6 have been recorded. While a small but significant propensity for electronically parity-allowed transitions is found, the observation of parity-forbidden electronic transitions is attributed to vibronic coupling that breaks the global inversion symmetry of the electronic wavefunction and localizes the core hole. The dependence of the scattering cross section on the polarization of the incident radiation and the scattering angle is interpreted in terms of local π/σ symmetry around the S–F bond. This symmetry selectivity prevails during the dissociation that occurs during the scattering process.

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Держатели документа:
Lund Univ, MAX IV Lab, Box 118, SE-22100 Lund, Sweden.
Uppsala Univ, Dept Phys & Astron, Box 516, SE-75120 Uppsala, Sweden.
Sorbonne Univ, F-75005 Paris, France.
CNRS, LCPMR, F-75005 Paris, France.
Synchrotron SOLEIL, LOrme Merisiers, BP 48, F-91192 Gif Sur Yvette, France.
Ctr Nacl Pesquisa Energia & Mat CNPEM, BR-10000 Campinas, Brazil.
Royal Inst Technol, Sch Biotechnol, Theoret Chem & Biol, S-10691 Stockholm, Sweden.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.
Stockholm Univ, AlbaNova Univ Ctr, Dept Phys, SE-10691 Stockholm, Sweden.

Доп.точки доступа:
Ekholm, V.; Chiuzbaian, G. S.; Sathe, C.; Nicolaou, A.; Guarise, M.; Simon, M.; Jaouen, N.; Luning, J.; Hague, C. F.; Gel'mukhanov, F.; Гельмуханов, Фарис Хафизович; Odelius, M.; Bjorneholm, O.; Rubensson, J-E; Swedish Research Council (VR)Swedish Research Council; Russian Science FoundationRussian Science Foundation (RSF) [16-12-10109]
}
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Electronic band structure and superconducting properties of SnAs / P. I. Bezotosnyi [et al.] // Phys. Rev. B. - 2019. - Vol. 100, Is. 18. - Ст. 184514, DOI 10.1103/PhysRevB.100.184514. - Cited References: 45. - The authors thank E. Z. Kuchinskii and M. V. Sadovskii for valuable discussions. This work was performed using equipment of the LPI Shared Facility Center and the resource center "Physical methods of surface investigation" (PMSI) of the Research park of Saint Petersburg State University. V.M.P. acknowledges Russian Foundation for Basic Research (RFBR) Grant No. 16-29-03330. P.I.B., K.A.D., A.V.S., K.S.P., A.V.M., A.S.U., A.Y.T., and S.Y.G. were supported within the state assignment of the Ministry of Science and Higher Education of the Russian Federation (Project No. 0023-2019-0005). A.G.R. acknowledges Saint Petersburg State University for research Grant No. 40990069. I.A.N., A.A.S., and N.S.P. acknowledge Russian Foundation for Basic Research (RFBR) Grants No. 17-02-00015 and No. 19-32-50001, the Program No. 12 of Fundamental Research of the Presidium of RAS. N.S.P. was also supported in part by the President of Russia grant for young scientists No. MK-1683.2019.2. . - ISSN 2469-9950. - ISSN 2469-9969

РУБ Materials Science, Multidisciplinary + Physics, Applied + Physics, Condensed Matter
Рубрики:
TOPOLOGICAL CRYSTALLINE INSULATOR
GAP STRUCTURE
SPECTROSCOPY
Аннотация: We report a comprehensive study of physical properties of the binary superconductor compound SnAs. The electronic band structure of SnAs was investigated using both angle-resolved photoemission spectroscopy (ARPES) in a wide binding energy range and density functional theory (DFT) within generalized gradient approximation (GGA). The DFT/GGA calculations were done including spin-orbit coupling for both bulk and (111) slab crystal structures. Comparison of the DFT/GGA band dispersions with ARPES data shows that the spectrum for the (111) slab much better describes ARPES data than that for the bulk. In addition, we studied experimentally superconducting properties of SnAs by specific heat, magnetic susceptibility, magnetotransport measurements, and Andreev reflection spectroscopy. Temperature dependencies of the superconducting gap and of the specific heat were found to be well consistent with those expected for the single band BCS superconductors with an isotropic s-wave order parameter. Despite spin-orbit coupling present in SnAs, our data show no signatures of a potential unconventional superconductivity, and the characteristic BCS ratio 2Δ/Tc=3.48–3.73 is very close to the BCS value in the weak coupling limit.

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Держатели документа:
PN Lebedev Phys Inst, VL Ginzburg Ctr High Tc Superconduct & Quantum Ma, Moscow 119991, Russia.
Natl Res Univ Higher Sch Econ, Fac Phys, Moscow 101000, Russia.
Russian Acad Sci, Inst Electrophys, Ural Branch, Ekaterinburg 620016, Russia.
RAS, SB, KSC, Kirensky Inst Phys,Fed Res Ctr, Krasnoyarsk 660036, Russia.
St Petersburg State Univ, Fac Phys, St Petersburg 198504, Russia.
St Petersburg State Univ, Res Pk, St Petersburg 198504, Russia.
St Petersburg State Univ, Lab Elect & Spin Struct Nanosyst, St Petersburg 198504, Russia.
Natl Res Univ Higher Sch Econ, Quantum Nanoelect Lab, Moscow 101000, Russia.

Доп.точки доступа:
Bezotosnyi, P. I.; Dmitrieva, K. A.; Sadakov, A. V.; Pervakov, K. S.; Muratov, A. V.; Usoltsev, A. S.; Tsvetkov, A. Yu.; Gavrilkin, S. Yu.; Pavlov, N. S.; Slobodchikov, A. A.; Слободчиков, А. А.; Vilkov, O. Yu.; Rybkin, A. G.; Nekrasov, I. A.; Pudalov, V. M.; Russian Foundation for Basic Research (RFBR)Russian Foundation for Basic Research (RFBR) [16-29-03330, 17-02-00015, 19-32-50001]; Ministry of Science and Higher Education of the Russian Federation [0023-2019-0005]; Saint Petersburg State University [40990069]; Presidium of RASRussian Academy of Sciences [12]; [MK-1683.2019.2]
}
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Observation of soft phonon mode in TbFe3(BO3)4 by inelastic neutron scattering / M. S. Pavlovskiy [et al.] // Phys. Rev. B. - 2018. - Vol. 97, Is. 5. - Ст. 054313, DOI 10.1103/PhysRevB.97.054313. - Cited References:40. - This research used resources at the Spallation Neutron Source, a DOE Office of Science User Facility operated by Oak Ridge National Laboratory. L.S.W. was supported by the Laboratory Directed Research and Development Program of Oak Ridge National Laboratory, managed by UT-Battelle, LLC, for the US DOE. The work was funded by RFBR, Government of Krasnoyarsk Territory, Krasnoyarsk Region Science and Technology Support Fund according to Research Project No. 16-42-243039. . - ISSN 2469-9950. - ISSN 2469-9969

РУБ Physics, Condensed Matter
Рубрики:
STRUCTURAL PHASE-TRANSITIONS
SINGLE-CRYSTAL
SPECTROSCOPY
Аннотация: The phonon dispersion in terbium iron borate TbFe3(BO3)4 has been measured by inelastic neutron scattering in a temperature range 180˂T˂350 K through the displacive structural transition at TS=192.5K and studied by ab initio calculations. Significant, but not complete, softening of the transverse acoustic (TA) branch has been observed at the corner of the Brillouin zone (Λ point) at temperatures T⪆TS, in full agreement with theoretical calculations. The TA soft mode undergoes considerable broadening at the Λ point near the transition temperature that can be attributed to the anharmonic interference between transverse acoustic and optical modes.

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Держатели документа:
Kirensky Inst Phys, Fed Res Ctr, Krasnoyarsk 660036, Russia.
Oak Ridge Natl Lab, Neutron Scattering Div, Oak Ridge, TN 37831 USA.
Oak Ridge Natl Lab, Neutron Technol Div, Oak Ridge, TN 37831 USA.

Доп.точки доступа:
Pavlovskiy, M. S.; Павловский, Максим Сергеевич; Shaykhutdinov, K. A.; Шайхутдинов, Кирилл Александрович; Wu, L. S.; Ehlers, G.; Temerov, V. L.; Темеров, Владислав Леонидович; Gudim, I. A.; Гудим, Ирина Анатольевна; Shinkorenko, A. S.; Шинкоренко, Алексей Сергеевич; Podlesnyak, A.; Laboratory Directed Research and Development Program of Oak Ridge National Laboratory; RFBR, Government of Krasnoyarsk Territory, Krasnoyarsk Region Science and Technology Support Fund [16-42-243039]
}
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Crystal structure, phase transition and structural deformations in iron borate (Y0.95Bi0.05)Fe3(BO3)4 in the temperature range 90–500 K / E. S. Smirnova [et al.] // Acta Crystallogr. B. - 2018. - Vol. 74. - P. 226-238, DOI 10.1107/S2052520618002962. - Cited References:27. - The following funding is acknowledged: Russian Foundation for Basic Research (award No. 17-02-00766) and Federal Agency of Scientific Organizations (Agreement No 007-GZ/Ch3363/26). . - ISSN 2052-5206

РУБ Chemistry, Multidisciplinary + Crystallography
Рубрики:
HIGH-PRESSURES
   GDFE3(BO3)4
   SPECTROSCOPY
   IFEFFIT
Кл.слова (ненормированные):
rare-earth iron borates -- crystal structure -- structural phase transition -- structural deformations
Аннотация: An accurate X-ray diffraction study of (Y0.95Bi0.05)Fe3(BO3)4 single crystals in the temperature range 90–500 K was performed on a laboratory diffractometer and used synchrotron radiation. It was established that the crystal undergoes a diffuse structural phase transition in the temperature range 350–380 K. The complexity of localization of such a transition over temperature was overcome by means of special analysis of systematic extinction reflections by symmetry. The transition temperature can be considered to be Tstr ≃ 370 K. The crystal has a trigonal structure in the space group P3121 at temperatures of 90–370 K, and it has a trigonal structure in the space group R32 at 375–500 K. There is one type of chain formed by the FeO6 octahedra along the c axis in the R32 phase. When going into the P3121 phase, two types of nonequivalent chains arise, in which Fe atoms are separated from the Y atoms by a different distance. Upon lowering the temperature from 500 to 90 K, a distortion of the Y(Bi)O6, FeO6, B(2,3)O3 coordination polyhedra is observed. The distances between atoms in helical Fe chains and Fe—O—Fe angles change non-uniformly. A sharp jump in the equivalent isotropic displacement parameters of O1 and O2 atoms within the Fe—Fe chains and fluctuations of the equivalent isotropic displacement parameters of B2 and B3 atoms were observed in the region of structural transition as well as noticeable elongation of O1, O2, B2, B3, Fe1, Fe2 atomic displacement ellipsoids. It was established that the helices of electron density formed by Fe, O1 and O2 atoms may be structural elements determining chirality, optical activity and multiferroicity of rare-earth iron borates. Compression and stretching of these helices account for the symmetry change and for the manifestation of a number of properties, whose geometry is controlled by an indirect exchange interaction between iron cations that compete with the thermal motion of atoms in the structure. Structural analysis detected these changes as variations of a number of structural characteristics in the c unit-cell direction, that is, the direction of the helices. Structural results for the local surrounding of the atoms in (Y0.95Bi0.05)Fe3(BO3)4 were confirmed by EXAFS and Mössbauer spectroscopies.

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Держатели документа:
Russian Acad Sci, Fed Sci Res Ctr Crystallog & Photon, Shubnikov Inst Crystallog, Moscow 119333, Russia.
Natl Res Ctr, Kurchatov Inst, Moscow 123182, Russia.
Russian Acad Sci, Inst Phys, Siberian Branch, Krasnoyarsk 660036, Russia.

Доп.точки доступа:
Smirnova, Ekaterina S.; Alekseeva, Olga A.; Dudka, Alexander P.; Artemov, V. V.; Zubavichus, Yan V.; Gudim, I. A.; Гудим, Ирина Анатольевна; Bezmaternykh, L. N.; Безматерных, Леонард Николаевич; Frolov, Kirill V.; Lyubutin, Igor S.; Russian Foundation for Basic Research [17-02-00766]; Federal Agency of Scientific Organizations [007-GZ/Ch3363/26]
}
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    Preparation and characterization of colloidal copper xanthate nanoparticles / Y. Mikhlin [et al.] // New J. Chem. - 2016. - Vol. 40, Is. 4. - P. 3059-3065, DOI 10.1039/c6nj00098c. - Cited References:50. - This research was supported by the Russian Science Foundation grant 14-17-00280. We thank Dr Roberto Felix Duarte (HZB) and bilateral program "German-Russian laboratory at BESSY II" for assistance with the X-ray absorption experiments. . - ISSN 1144-0546. - ISSN 1369-9261
   Перевод заглавия: Получение и исследование коллоидных наночастиц ксантогената меди

РУБ Chemistry, Multidisciplinary
Рубрики:
X-ray-absorption
   Self-assembled monolayers
   Sulfide nanoparticles
   Electronic-structure
   Waste-water
   Complexes
   Flotation
   Spectroscopy
   Adsorption
   Oxidation
Аннотация: Despite the important role of metal xanthates in a number of industrial processes and emerging applications, no attempts have been made to prepare the metal xanthate nanoparticles and to study colloidal solutions of insoluble heavy metal xanthates. Here, we examined the formation of colloidal copper xanthate particles during the reactions of aqueous solutions of cupric sulfate and various potassium xanthates, which occur in flotation and water treatment slurries and can be used to manufacture nanoparticles for materials science (e.g., as precursors for copper sulfide nanoparticles and biomedicine). The products were characterized using UV-vis absorption, dynamic light scattering, zeta potential measurements, transmission electron microscopy (TEM), electron diffraction, Fourier transform infrared spectroscopy, thermogravimetry, X-ray photoelectron spectroscopy, and X-ray absorption spectroscopy (XANES). Colloidal copper xanthates with compositions of ROCSSCu (R = ethyl, isopropyl, butyl, isobutyl, and amyl groups), disordered structures and average diameters of 20–80 nm easily formed and aggregated and were stable for at least several hours, especially if excessive xanthate was used. The hydrodynamic diameters of the nanoparticles were smaller at lower temperatures. Dixanthogens, which were produced in the reactions along with ROCSSCu, seemed to promote nanoparticle aggregation and precipitated with the copper xanthate, affecting their thermal decomposition. The TEM micrographs and S K- and Cu K-edge XANES spectra revealed core/shell particle morphologies, likely with Cu(I) bonded to four S atoms in the core and reduced copper coordination in the shell.

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Держатели документа:
Russian Acad Sci, Inst Chem & Chem Technol, Siberian Branch, Akad 50-24, Krasnoyarsk 6600036, Russia.
Siberian Fed Univ, Svobodny Pr 79, Krasnoyarsk 660041, Russia.
Russian Acad Sci, Siberian Branch, Kirensky Inst Phys, Akad 50-38, Krasnoyarsk 660036, Russia.

Доп.точки доступа:
Mikhlin, Y. L.; Михлин, Юрий Леонидович; Vorobyev, S.; Saikova, S. V.; Сайкова, С. В.; Tomashevich, Y.; Fetisova, O.; Kozlova, S.; Zharkov, S. M.; Жарков, Сергей Михайлович; Russian Science Foundation [14-17-00280]
}
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NMR applications for polymer composite materials moisture uptake investigation / V. M. Bouznik [et al.] // Appl. Magn. Reson. - 2016. - Vol. 47, Is. 3. - P. 321-334, DOI 10.1007/s00723-015-0748-2. - Cited References: 41. - This research was performed with the financial support of Russian Foundation for Basic Research (project no. 14-29-10178 ofi_m). . - ISSN 0937-9347

РУБ Physics, Atomic, Molecular & Chemical + Spectroscopy
Рубрики:
FIELD GRADIENT NMR
   REINFORCED EPOXY COMPOSITES
   WATER SELF-DIFFUSION
   TRANSPORT
   GLASS
   SYSTEM
   SPECTROSCOPY
   TEMPERATURE
   ABSORPTION
   ADHESIVE
Аннотация: The 1H nuclear magnetic resonance (NMR) spectroscopy, NMR imaging, and pulsed field gradient NMR (PFG NMR) were applied for comparative study of moisture–polymer composite materials (PCM) interaction. The water uptake in PCM reinforced by aramid and carbon fibers was measured by NMR spectroscopy techniques. The aramid fiber-reinforced PCM absorbs water more intensively compared with PCM reinforced by carbon fiber, but both of them are retaining water inside of pores without formation of chemical bonds. Using NMR imaging the spatial distribution of water absorbed was visualized; preferable water pathways and influence of surface treatment on water-resistant properties were revealed. It was found that the surface rough treatment sufficiently improves the water absorption, but penetration of water molecules is still occurring only through the surfaces and it happens within a thin layer. PFG NMR technique revealed influence of pore structure on moisture–PCM interaction; it was found that additionally to strong hydrophobic properties of carbon fiber, the smaller total volume of pores sufficiently decrease the water uptake. Results achieved in this work demonstrate efficiency of NMR methods applied all together for investigation of PCM, and information obtained is practically important when designing advanced PCM with required properties. © 2016, Springer-Verlag Wien.

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Держатели документа:
Institute of Problems of Chemical Physics RAS, Chernogolovka, Russian Federation
All-Russian Scientific Research Institute of Aviation Materials, Moscow, Russian Federation
Kirensky Institute of Physics SB RAS, Krasnoyarsk, Russian Federation
Institute of Chemistry and Chemical Technology SB RAS, Krasnoyarsk, Russian Federation
Science Center in Chernogolovka of the Russian Academy of Sciences, Chernogolovka, Russian Federation

Доп.точки доступа:
Bouznik, V. M.; Morozov, E. V.; Морозов, Евгений Владимирович; Avilova, I. A.; Volkov, V. I.
}
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Gorelik, V. S.
Raman scattering in sodium nitrite crystals near the phase transition / V. S. Gorelik, A. Y. Pyatyshev, A. S. Krylov // Phys. Solid State. - 2016. - Vol. 58, Is. 1. - P. 170-176, DOI 10.1134/S1063783416010133. - Cited References: 39. - This study was supported by the Russian Foundation for Basic Research (project nos. 12-02-00491, 13-02-00449, 13-02-90420, and 14-02-00190). . - ISSN 1063-7834

РУБ Physics, Condensed Matter
Рубрики:
NaNO2
   SPECTROSCOPY
   DEPENDENCE
   SPECTRUM
   SEARCH
   MODES
Аннотация: Optical Raman spectra of a ferroelectric sodium nitrite crystal have been detected in a wide spectrum range at various temperatures, including the region of the ferroelectric phase transition. A manifestation of a transverse soft polar mode of the A1(z) type responsible for the ferroelectric phase transition has been discovered in the spectrum at room temperature. This mode has been found to become overdamped even far from the ferroelectric phase transition temperature. This mode also appears as a central peak under heating. It has been found that the pseudoscalar mode of the A2 type has the highest intensity in the Raman spectrum of sodium nitrite. The frequency corresponding to the maximum intensity of this mode in the Raman spectrum varies from 130 cm–1 at 123 K to 106 cm–1 at T = 513 K. A fair agreement of the experimental data for the A1(z) mode with the Lyddane–Sachs–Teller relation has been established. The polariton curves for the A1(z) polar mode and the dispersion curves for axinons has been plotted. © 2016, Pleiades Publishing, Ltd.

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Публикация на русском языке Горелик, Владимир Семенович. Комбинационное рассеяние света в области фазового перехода в кристаллах нитрита натрия [Текст] / В. С. Горелик, А. Ю. Пятышев, А. С. Крылов // Физ. тверд. тела : Физико-технический институт им. А. Ф. Иоффе РАН, 2016. - Т. 58 Вып. 1. - С. 163-169

Держатели документа:
Lebedev Physical Institute, Russian Academy of Sciences, Leninskii pr. 53, Moscow, Russian Federation
Bauman Moscow State Technical University, Vtoraya Baumanskaya ul. 5, Moscow, Russian Federation
Kirensky Institute of Physics, Siberian Branch, Russian Academy of Sciences, Akademgorodok 50, Krasnoyarsk, Russian Federation

Доп.точки доступа:
Pyatyshev, A. Y.; Krylov, A. S.; Крылов, Александр Сергеевич
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10.

    Gorelik, V. S.
    Raman light scattering in sodium nitrite crystals / V. S. Gorelik, A. Y. Pyatyshev, A. S. Krylov // Bull. Lebedev Phys. Inst. - 2016. - Vol. 43, Is. 5. - P. 167-173, DOI 10.3103/S1068335616050043. - Cited References:37. - This study was supported by the Russian Foundation for Basic Research, projects nos. 12-02-00491, 13-02-00449,13-02-90420, 14-02-00190. . - ISSN 1068-3356. - ISSN 1934-838X
Рубрики:
NANO2
   PHASE
   SPECTROSCOPY
   PARAPHOTONS
   DEPENDENCE
   SPECTRUM
   SEARCH
Кл.слова (ненормированные):
sodium nitrite -- Raman scattering -- spectrum -- polar mode -- polariton -- ferroelectric -- dispersion curves
Аннотация: Raman light scattering spectra of a ferroelectric sodium nitrite crystal is studied in the lattice mode region as the temperature is lowered from room temperature to 123 K. The existence of a Raman satellite corresponding to the soft lattice mode, i.e., transverse polar vibration responsible for the ferroelectric phase transition, is established for the first time. It is found that the intensity of the Raman scattering by the pseudo-scalar low-frequency A (2) mode exceeds the intensity of other lattice variations by an order of magnitude.

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Публикация на русском языке Горелик, Владимир Семенович. Комбинационное рассеяние света в кристаллах нитрита натрия [Текст] / В. С. Горелик, А. Ю. Пятышев, А. С. Крылов // Кратк. сообщ. по физ. : Физический институт им. П. Н. Лебедева РАН, 2016. - Т. 43 № 5. - С. 26-36

Держатели документа:
Russian Acad Sci, PN Lebedev Phys Inst, Leninskii Pr 53, Moscow 119991, Russia.

Доп.точки доступа:
Pyatyshev, A. Yu.; Krylov, A. S.; Крылов, Александр Сергеевич; Russian Foundation for Basic Research [12-02-00491, 13-02-00449, 13-02-90420, 14-02-00190]
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