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1.


   
    High ionic conductivity of K5-xTlx(Mg0.5Hf1.5)(MoO4)6 (0 ≤ х ≤ 5) solid solutions / V. G. Grossman, M. S. Molokeev, J. G. Bazarova, B. G. Bazarov // Solid State Sci. - 2022. - Vol. 134. - Ст. 107027, DOI 10.1016/j.solidstatesciences.2022.107027. - Cited References: 39. - The work was supported by Basic Project of BINM SB RAS №0273-2021-0008. Structural analysis of materials in this study was partly supported by the Research Grant No. 075-15-2019-1886 from the Government of the Russian Federation . X-ray powder diffraction and thermal analysis were obtained using the equipment of the Collective Use Center BINM SB RAS . - ISSN 1293-2558
   Перевод заглавия: Высокая ионная проводимость твердых растворов K5-xTlx(Mg0.5Hf1.5)(MoO4)6 (0 ≤ х ≤ 5)
Кл.слова (ненормированные):
Synthesis -- Thallium -- Potassium -- Molybdates -- DSC -- Conducting material
Аннотация: Novel K5-xTlx(Mg0.5Hf1.5)(MoO4)6 (0 ≤ х ≤ 5) oxides were successfully synthesized by solid state reaction. The results indicate the formation of a continuous series of solid solutions with the NASICON-like structure (sp. gr. R3¯c) in the composition range 0 < x < 5. The unit-cell parameters of the solid solutions increase linearly with composition, as a consequence of thallium substitution for potassium. The cation conductivity of Tl5Mg0.5Hf1.5(MoO4)6 has been shown to exceed the conductivity of the parent potassium magnesium hafnium molybdate. The highest total conductivity of 2.49 × 10−3 S/cm was found at 831 K for Tl5Mg0.5Hf1.5(MoO4)6.

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Держатели документа:
Baikal Institute of Nature Management, SB RAS, Sakhyanovoy St., 6, Ulan-Ude, 670047, Russian Federation
Kirensky Institute of Physics, Federal Research Center KSC, Siberian Branch, Academy of Sciences, 50 / 38 Akademgorodok, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, 82 Svobodniy Av., Krasnoyarsk, 660041, Russian Federation
Department of Physics, Far Eastern State Transport University, Serysheva str. 47, Khabarovsk, 680021, Russian Federation

Доп.точки доступа:
Grossman, V. G.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Bazarova, J. G.; Bazarov, B. G.
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2.


   
    Solid-state reaction in Cu/a-Si nanolayers: A comparative study of STA and electron diffraction data / E. T. Moiseenko, V. V. Yumashev, R. R. Altunin [и др.] // Materials. - 2022. - Vol. 15, Is. 23. - Ст. 8457, DOI 10.3390/ma15238457. - Cited References: 45. - This work was supported by the Russian Science Foundation under grant # 22-13-00313 . - ISSN 1996-1944
   Перевод заглавия: Твердофазная реакция в нанослоях Cu/a-Si: сравнительное исследование данных, полученных методами СТА и дифракции электронов
Кл.слова (ненормированные):
copper silicide -- thin films -- nanolayer -- solid-state reaction -- phase formation -- kinetics -- activation energy -- enthalpy -- DSC -- electron diffraction
Аннотация: The kinetics of the solid-state reaction between nanolayers of polycrystalline copper and amorphous silicon (a-Si) has been studied in a Cu/a-Si thin-film system by the methods of electron diffraction and simultaneous thermal analysis (STA), including the methods of differential scanning calorimetry (DSC) and thermogravimetry (TG). It has been established that, in the solid-state reaction, two phases are formed in a sequence: Cu + Si → η″-Cu3Si → γ-Cu5Si. It has been shown that the estimated values of the kinetic parameters of the formation processes for the phases η″-Cu3Si and γ-Cu5Si, obtained using electron diffraction, are in good agreement with those obtained by DSC. The formation enthalpy of the phases η″-Cu3Si and γ-Cu5Si has been estimated to be: ΔHη″-Cu3Si = −12.4 ± 0.2 kJ/mol; ΔHγ-Cu5Si = −8.4 ± 0.4 kJ/mol. As a result of the model description of the thermo-analytical data, it has been found that the process of solid-state transformations in the Cu/a-Si thin-film system under study is best described by a four-stage kinetic model R3 → R3 → (Cn-X) → (Cn-X). The kinetic parameters of formation of the η″-Cu3Si phase are the following: Ea = 199.9 kJ/mol, log(A, s−1) = 20.5, n = 1.7; and for the γ-Cu5Si phase: Ea = 149.7 kJ/mol, log(A, s−1) = 10.4, n = 1.3, with the kinetic parameters of formation of the γ-Cu5Si phase being determined for the first time.

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Держатели документа:
Laboratory of Electron Microscopy, Siberian Federal University, 79 Svobodny Ave., 660041 Krasnoyarsk, Russia
Institute of Chemistry and Chemical Technology, Federal Research Center KSC SB RAS, Akademgorodok 50/24, 660036 Krasnoyarsk, Russia
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Akademgorodok 50/38, 660036 Krasnoyarsk, Russia

Доп.точки доступа:
Moiseenko, E. T.; Yumashev, V. V.; Altunin, R. R.; Zeer, G. M.; Nikolaeva, N. S.; Belousov, O. V.; Zharkov, S. M.; Жарков, Сергей Михайлович
}
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3.


   
    Tetragonal to cubic transition of Sr0.8Dy0.2CoO3-δ and oxygen mobility: TG-DSC-XRD study / S. Vereshchagin, V. Dudnikov, Y. Orlov, L. Solovyov // J. Alloys Compd. - 2021. - Vol. 860. - Ст. 158257, DOI 10.1016/j.jallcom.2020.158257. - Cited References: 35. - This work was conducted within the framework of the budget project (Project No. АААА-А17-117021310222-4) for Institute of Chemistry and Chemical Technology SB RAS using the equipment of Krasnoyarsk Regional Research Equipment Centre of SB RAS and in part was funded by Russian Foundation for Basic Research (projects 19-03-00017), RFBR and BRFBR (project 18-52-00017), Russian Foundation for Basic Research, Government of Krasnoyarsk Territory, Krasnoyarsk Regional Fund of Science (project 18-42-243004) . - ISSN 0925-8388
Кл.слова (ненормированные):
Ceramics -- Perovskite -- Phase transitions -- Oxygen mobility -- Thermal analysis -- X-ray diffraction
Аннотация: Processes of ordering (d-o) and disordering (o-d) of Sr2+/Dy3+ cations in a single-phase Sr0.8Dy0.2CoO3-δ was investigated by TG-DSC and XRD as a function of heating/cooling rate (β = 2,10,20,50,99 K min−1 and ~50 K/s) in 20% O2-Ar flow. According to DSC data the interconversion of disordered cubic (c) and ordered tetragonal (t) structure appears at 1276–1328 K as a first-order phase transition; the temperature and enthalpy of o-d transformation have only slight dependence on β whereas the characteristics of reversed d-o process vary greatly with cooling rate. XRD powder patterns of all samples showed no indications of a simultaneous presence of c+t domains, pointing to a single phase composition (c or t). It was suggested that the observed behavior is a consequence of two simultaneous interconnected processes of A-sublattice melting and cation/ (anion vacancy) ordering. A rarely used novel TG-DSC method based on variable gas phase composition was utilized to study properties of mobile oxygen over Sr0.8Dy0.2CoO3-δ samples. It was shown that the appearance of tetragonal phase reduces both oxygen mobility and its bonding energy, the latter decreasing substantially only at high degree of Sr2+/Dy3+ ordering.

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Держатели документа:
Institute of Chemistry and Chemical Technology, Federal Research Center “Krasnoyarsk Scientific Center, Russian Academy of Sciences, Siberian Branch”, Krasnoyarsk, 660036, Russian Federation
Kirensky Institute of Physics, Federal Research Center “Krasnoyarsk Scientific Center, Russian Academy of Sciences, Siberian Branch”, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Institute of Engineering Physics and Radio Electronics, Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Vereshchagin, S.; Dudnikov, V. A.; Дудников, Вячеслав Анатольевич; Orlov, Yu. S.; Орлов, Юрий Сергеевич; Solovyov, L.
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4.


   
    Potassium and thallium conductors with a trigonal structure in the M2MoO4–Cr2(MoO4)3–Hf(MoO4)2 (M = K, Tl) systems: Synthesis, structure, and ionic conductivity / V. G. Grossman, M. S. Molokeev, B. G. Bazarov, J. G. Bazarova // J. Alloys Compd. - 2021. - Vol. 873. - Ст. 159828, DOI 10.1016/j.jallcom.2021.159828. - Cited References: 62. - The work was supported by Basic Project of BINM SB RAS № 0273-2021-0008 . Research was conducted using equipment of the CCU BINM SB RAS (Ulan-Ude, Russia). Structural analysis of materials in this study was partly supported by the Research Grant No. 075-15-2019-1886 from the Government of the Russian Federation . - ISSN 0925-8388
   Перевод заглавия: Калиевые и таллиевые проводники с тригональной структурой в системах M2MoO4-Cr2(MoO4)3–Hf(MoO4)2 (M = K, Tl): синтез, структура и ионная проводимость
Кл.слова (ненормированные):
Synthesis -- Thallium -- Potassium -- Molybdates -- Phase diagram -- DSC -- Conducting material
Аннотация: The triple molybdates M5CrHf(MoO4)6 (M = K, Tl) and TlCrHf0.5(MoO4)3 were found upon studying the corresponding ternary molybdate systems M2MoO4–Cr2(MoO4)3–Hf(MoO4)2 (M = K, Tl) in the subsolidus region using X-ray powder diffraction. The crystal structures of M5CrHf(MoO4)6 (M = K, Tl) and TlCrHf0.5(MoO4)3 are refined by Rietveld method. M5CrHf(MoO4)6 (M = K, Tl) crystallizes in space group Rc with unit cell parameters: a = b = 10.45548 (5), c = 37.24614 (3) Å, V = 3526.14 (4) Å3, Z = 6 for K5CrHf(MoO4)6 and a = b = 10.53406 (12), c = 37.6837 (5) Å, V = 3621.39 (9) Å3, Z = 6 for Tl5CrHf(MoO4)6. TlCrHf0.5(MoO4)3 crystallizes in space group R with unit cell parameters: a = b = 12.9710 (2), c = 11.7825 (2) Å, V = 1716.78 (6) Å3, Z = 6. The thermal stability and electrical conductivity of the new compounds were investigated. Electrical conductivity measurements gave high values for the triple molybdates M5CrHf(MoO4)6 (M = K, Tl) (σ = 5.22 × 10−4 S / cm for K5CrHf(MoO4)6, σ = 1.1 × 10−2 S / cm for Tl5CrHf(MoO4)6 at 773 K) and relatively low values for the triple molybdate TlCrHf0.5(MoO4)3 (σ = 4.42 × 10−6 S / cm at 773 K).

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Держатели документа:
Baikal Institute of Nature Management, SB RAS, Sakhyanovoy St., 6, Ulan-Ude, 670047, Russian Federation
Kirensky Institute of Physics, Federal Research Center KSC, Siberian Branch, Academy of Sciences, 50/38 Akademgorodok, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, 82 Svobodniy Av., Krasnoyarsk, 660041, Russian Federation
Department of Physics, Far Eastern State Transport University, Serysheva str. 47, Khabarovsk, 680021, Russian Federation

Доп.точки доступа:
Grossman, V. G.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Bazarov, B. G.; Bazarova, J. G.
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5.


   
    New triple molybdate K5ScHf(MoO4)6: Synthesis, properties, structure and phase equilibria in the M2MoO4–Sc2(MoO4)3–Hf(MoO4)2 (M = Li, K) systems / V. G. Grossman, J. G. Bazarova, M. S. Molokeev, B. G. Bazarov // J. Solid State Chem. - 2020. - Vol. 283. - Ст. 121143, DOI 10.1016/j.jssc.2019.121143. - Cited References: 53. - This study was carried out within the state assignment of FASO of Russia (Theme No 0339-2016-0007) as well was supported by RFBR Grants 18-08-00799 and 18-03-00557 . - ISSN 0022-4596
   Перевод заглавия: Новый тройной молибдат K5ScHf(MoO4)6: синтез, свойства, структура и фазовые равновесия в системах M2MoO4-Sc2(MoO4)3-Hf(MoO4)2 (M = Li, K)
Кл.слова (ненормированные):
Synthesis -- Molybdates -- X-ray diffraction -- DSC -- Electric properties
Аннотация: Subsolidus phase relations in the M2MoO4–Sc2(MoO4)3–Hf(MoO4)2 (M ​= ​Li, K) systems have been studied by the method of “intersecting cuts”. No new triple molybdates have been identified in the Li2MoO4–Sc2(MoO4)3–Hf(MoO4)2 system and a new triple molybdate K5ScHf(MoO4)6 is formed in the K2MoO4–Sc2(MoO4)3–Hf(MoO4)2 system. The structure of K5ScHf(MoO4)6, have been determined in space group Rc through Rietveld analysis of X-ray powder diffraction data. The melting point of molybdate is 999 ​K. The compound has high ion conductivity (about 10−3 ​S ​cm−1).

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Держатели документа:
Baikal Institute of Nature Management, Siberian Branch, Russian Academy of Sciences, Sakhyanovoy St., 6, Ulan-Ude, Buryat Republic 670047, Russian Federation
Kirensky Institute of Physics, Federal Research Center KSC, Siberian Branch, RAS, 50 / 38 Akademgorodok, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, 82 Svobodniy Av., Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Grossman, V. G.; Bazarova, J. G.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Bazarov, B. G.
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6.


   
    Thallium ionic conductivity of new thallium indium hafnium molybdate ceramics / V. G. Grossman, J. G. Bazarova, M. S. Molokeev, B. G. Bazarov // Ionics. - 2020. - Vol. 26. - P. 6157-6165, DOI 10.1007/s11581-020-03739-7. - Cited References: 60. - This study was carried out within the state assignment of FASO of Russia (Theme No 0339-2016-0007) as well was supported by RFBR Grants 18-08-00799 and 18-03-00557 . - ISSN 0947-7047. - ISSN 1862-0760
   Перевод заглавия: Таллий-ионная проводимость новой керамики на основе таллия, индия, гафния, молибдата
РУБ Chemistry, Physical + Electrochemistry + Physics, Condensed Matter
Рубрики:
POSITIVE ELECTRODE MATERIAL
   CRYSTAL-STRUCTURE

   TRIPLE MOLYBDATE

Кл.слова (ненормированные):
Synthesis -- Thallium -- Molybdates -- Phase diagram -- DSC -- Conducting material
Аннотация: In the process of studying the system Tl2MoO4–In2(MoO4)3–Hf(MoO4)2, a new thallium indium hafnium molybdate was found. The crystal structure of the molybdate Tl5InHf(MoO4)6 was determined in the centrosymmetric space group R3¯c (a = 10.63893 (5) Å, c = 38.1447(3) Å; V = 3739.04 (4) Å3, Z = 6). The structure is a three-dimensional framework consisting of alternating (Hf,In)O6-octahedra connected by МоО4-tetrahedra. Each octahedron has common vertices with tetrahedra. The atoms arranged in this way form channels extended along with the a and b axes, in which thallium atoms are located. The conductivity behavior of Tl5InHf(MoO4)6 ceramics was studied in the temperature range from 300 to 870 K. The conductivity of the heavy cations of thallium is activated with increasing temperature.

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Держатели документа:
Russian Acad Sci, Baikal Inst Nat Management, Siberian Branch, Sakhyanovoy St 6, Ulan Ude 670047, Buryat Republic, Russia.
Russian Acad Sci, Fed Res Ctr KSC, Kirensky Inst Phys, Siberian Branch, 50-38 Akademgorodok, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, 82 Svobodniy Av, Krasnoyarsk 660041, Russia.

Доп.точки доступа:
Grossman, Victoria G.; Bazarova, J. G.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Bazarov, B. G.; RFBRRussian Foundation for Basic Research (RFBR) [0339-2016-0007]; [18-08-00799]; [18-03-00557]
}
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7.


   
    Exploration of structural, vibrational and spectroscopic properties of self-activated orthorhombic double molybdate RbEu(MoO4)2 with isolated MoO4 units / V. V. Atuchin, A. S. Aleksandrovsky, B. G. Bazarov [et al.] // J. Alloy. Compd. - 2019. - Vol. 785. - P. 692-697, DOI 10.1016/j.jallcom.2019.01.013. - Cited References: 42. - The reported study was funded by RFBR according to research projects 16-52-48010, 17-52-53031 and 18-03-00557. Besides, this study was supported by the Ministry of Science and Higher Education of the Russian Federation (project 0339-2016-0007). The work was supported by Act 211 Government of the Russian Federation, contract No 02.A03.21.0011. Additionally, the work was partially supported by the Ministry of Education and Science of the Russian Federation (4.1346.2017/4.6). . - ISSN 0925-8388. - ISSN 1873-4669
   Перевод заглавия: Исследование структурных, колебательных и спектроскопических свойств самоактивированного орторомбического двойного молибдата RbEu(MoO4)2 с изолированными группами MoO4
РУБ Chemistry, Physical + Materials Science, Multidisciplinary + Metallurgy & Metallurgical Engineering
Рубрики:
MORPHOLOGY-CONTROLLED SYNTHESIS
   LUMINESCENCE PROPERTIES

Кл.слова (ненормированные):
Rubidium europium molybdate -- Solid state reaction -- Rietveld refinement -- DSC -- Raman luminescence
Аннотация: RbEu(MoO4)2 is synthesized by the two-step solid state reaction method. The crystal structure of RbEu(MoO4)2 is defined by Rietveld analysis in space group Pbcn with cell parameters a = 5.13502(5), b = 18.8581(2) and c = 8.12849(7) Å, V = 787.13(1) Å3, Z = 4 (RB = 0.86%). This molybdate possesses its phase transition at 817 K and melts at 1250 K. The Raman spectra were measured with the excitation at λ = 1064 and 514.5 nm. The photoluminescence spectrum is evaluated under the excitation at 514.5 nm. The absolute domination of hypersensitive 5D0→7F2 transition is observed. The ultranarrow 5D0→7F0 transition in RbEu(MoO4)2 is positioned at 580.2 nm being 0.2 nm blue shifted, with respect to that in Eu2(MoO4)3.

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Держатели документа:
SB RAS, Lab Opt Mat & Struct, Inst Semicond Phys, Novosibirsk, Russia.
Tomsk State Univ, Funct Elect Lab, Tomsk 634050, Russia.
South Ural State Univ, Lab Single Crystal Growth, Chelyabinsk 454080, Russia.
Kemerovo State Univ, Res & Dev Dept, Kemerovo 650000, Russia.
SB RAS, Kirensky Inst Phys, Lab Coherent Opt, Fed Res Ctr KSC, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Dept Photon & Laser Technol, Krasnoyarsk 660079, Russia.
SB RAS, Baikal Inst Nat Management, Lab Oxide Syst, Ulan Ude 670047, Russia.
Buryat State Univ, Ulan Ude 670000, Russia.
Ind Univ Tyumen, Dept Gen & Special Chem, Tyumen 625000, Russia.
SB RAS, Inst Semicond Phys, Lab Nanodiagnost & Nanolithog, Novosibirsk 630090, Russia.
SB RAS, Kirensky Inst Phys Fed Res Ctr KSC, Lab Mol Spect, Krasnoyarsk 660036, Russia.
SB RAS, Inst Inorgan Chem, Lab Funct Films & Coatings, Novosibirsk 630090, Russia.
SB RAS, Lab Crystal Phys, Kirensky Inst Phys, Fed Res Ctr KSC, Krasnoyarsk 660036, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
Siberian Fed Univ, Krasnoyarsk 660079, Russia.
SB RAS, Inst Automat & Elect, Lab Condensed Matter Spect, Novosibirsk 630090, Russia.

Доп.точки доступа:
Atuchin, V. V.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Bazarov, B. G.; Bazarova, J. G.; Chimitova, Olga D.; Denisenko, Yuriy G.; Gavrilova, T. A.; Krylov, A. S.; Крылов, Александр Сергеевич; Maximovskiy, Eugene A.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Pugachev, Alexey M.; Surovtsev, Nikolay V.; RFBR [16-52-48010, 17-52-53031, 18-03-00557]; Ministry of Science and Higher Education of the Russian Federation [0339-2016-0007]; Act 211 Government of the Russian Federation [02.A03.21.0011]; Ministry of Education and Science of the Russian Federation [4.1346.2017/4.6]
}
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8.


    Верещагин, Сергей Николаевич.
    Применение ТГ/ДСК-анализа c программированным составом газовой фазы для изучения фазового перехода порядок-беспорядок в нестехиометрическом Sr-Dy-кобальтате / С. Н. Верещагин, В. А. Дудников, Ю. С. Орлов // J. Sib. Fed. Univ. Chem. - 2018. - Vol. 11, Is. 4. - P. 507-517 ; Журн. СФУ. Химия, DOI 10.17516/1998-2836-0095. - Библиогр.: 17. - Исследование выполнено при финансовой поддержке Российского фонда фундаментальных исследований, Правительства Красноярского края, Красноярского краевого фонда науки в рамках научного проекта No 18-42-243004 и проекта фундаментальных исследований СО РАН V.45.3.3. . - ISSN 1998-2836. - ISSN 2313-6049
   Перевод заглавия: Application of TG/DSC analysis under variable gas phase composition to study order-disorder transition in nonstoichiometric Sr-Dy-cobaltate
РУБ Chemistry, Multidisciplinary
Рубрики:
PEROVSKITE
   OXYGEN

Кл.слова (ненормированные):
перовскит -- порядок-беспорядок -- фазовый переход -- ТГ -- ДСК -- perovskite -- order-disorder -- phase transition -- TG -- DSC
Аннотация: Методом термического анализа (ТГ/ДСК) в условиях постоянного и программированного состава газовой фазы изучено влияние скорости закалки на полноту перехода кубического разупорядоченного нестехиометрического перовскита (I) Sr(0.8)Dy(0.2)CoO(3-d) в тетрагональную модификацию (II) с упорядоченным расположением катионов Sr/Dy и анионных вакансий, а также взаимосвязь степени превращения I в II с количеством мобильного кислорода и его энергетическими характеристиками. Показано, что фазовое превращение протекает как фазовый переход первого рода, процесс образования структуры II контролируется кинетическими факторами, а использование скоростей охлаждения 3-99 К/мин позволяет получить образцы, формально соответствующие 98-30 % превращению I в II; при этом как количество подвижного кислорода, так и энтальпия его удаления из образца нелинейно зависят от полноты перехода I в II.
For the first time a method of TG/DSC analysis under constant and variable gas phase composition was applied to reveal interconnection between quenching ramp rates and degree of phase transformation of cubic nonstoichiometric disordered perovskite (I) Sr(0.8)Dy(0.2)CoO(3-d) to tetragonal structure (II) with ordered Sr/Dy cations and anion vacancies. It was shown that the transformation is a first order phase transition and the ordering process is kinetically controlled. Based on the experimental transition enthalpy it was found that a formal conversion degree of I to II was 98-30% under cooling ramp rates 3-99 K/min. Non-linear relationship between the completeness of I-to-II transformation and mobile oxygen characteristics (content and the enthalpy of O-removal) was demonstrated.

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Держатели документа:
SB RAS, FRC Krasnoyarsk Sci Ctr, Inst Chem & Chem Technol, 50-24 Akademgorodok, Krasnoyarsk 660036, Russia.
SB RAS, FRC Krasnoyarsk Sci Ctr, Kirensky Inst Phys, 50-38 Akademgorodok, Krasnoyarsk 660036, Russia.

Доп.точки доступа:
Дудников, Вячеслав Анатольевич; Dudnikov, V. A.; Орлов, Юрий Сергеевич; Orlov, Yu. S.; Vereshchagin S. N.

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9.


   
    Joint studies of water phase transitions in Na-bentonite clay by calorimetric and dielectric methods / V. L. Mironov [et al.] // Cold Reg. Sci. Technol. - 2018. - Vol. 153. - P. 172-180, DOI 10.1016/j.coldregions.2018.04.010. - Cited References: 30. - The authors are sincerely grateful to the reviewers for their concerned analyses of the content of this paper and providing the valuable helpful discussion that allowed us to introduce many principle improvements in the text of the manuscript. This work was supported by Programs II.12.1. Fundamental Research SB RAS, Russia. . - ISSN 0165-232X
   Перевод заглавия: Совместные исследования фазовых переходов воды в Na-бентонитовой глине калориметрическим и диэлектрическим методами
Кл.слова (ненормированные):
Frozen soil -- Non-freezing water -- Unfrozen water -- Bound water -- Phase transitions -- DSC -- Dielectric permittivity -- Dielectric model
Аннотация: The present study consisted of an experimental investigation of phase transitions of soil water contained in moist Na-bentonite clay, using the differential scanning calorimetry (DSC) method, within the temperature range from −40 to 20 °C. Based on the results of DSC analysis, the following components of soil water were found in the frozen bentonite: non-freezing water, unfrozen water and ice. The proposed method of processing the obtained experimental calorimetric data allowed us to determine the temperature dependencies of the content of particular soil water components. Latent heat of fusion was found in two cases, namely: where the ice was transformed into bound or unbound unfrozen soil water. The results of the investigation into phase transitions, obtained via calorimetric measurements, were used to substantiate the method for studying the phase transitions of soil water by dielectric measurements. With this in mind, complex relative permittivity testing was conducted on the same moist Na-bentonite clay, in the temperature range from −30 to 0 °C and a gravimetric moisture range from the dry soil to 1 g/g. Based on the results of these dielectric tests and a refractive dielectric mixture model (RDMM), the following components of water were identified in the frozen soil: tightly bound water, loosely bound water, unbound water and ice. The dependences of the content of these components of soil water on the temperature were calculated. It was shown that the increase in the mass of unfrozen loosely bound water, as a result of a decrease in the ice mass, determined with dielectric measurements, is quantitatively consistent with the dependence calculated using calorimetric testing. This proves that the changes of the mass of the loosely bound water, determined by dielectric measurements, is a result of the phase transition and the corresponding temperature dependence can be used to determine the characteristics of these phase transitions.

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Держатели документа:
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, Russian Federation
Krasnoyarsk, Russia Institute of Engineering Physics and Radioelectronics, Siberian State University, Krasnoyarsk, Russian Federation

Доп.точки доступа:
Mironov, V. L.; Миронов, Валерий Леонидович; Karavayskiy, A. Yu.; Каравайский, Андрей Юрьевич; Lukin, Y. I.; Лукин, Юрий Иванович; Pogoreltsev, E. I.; Погорельцев, Евгений Ильич
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10.


    Верещагин, Сергей Николаевич.
    Изучение подвижного кислорода в упорядоченном/разупорядоченном нестехиометрическом кобальтате Sr-Gd методом синхронного термического анализа / С. Н. Верещагин, В. А. Дудников, Л. А. Соловьев // Журн. СФУ. Химия. - 2017. - Т. 10, № 3. - С. 346-357 ; J. Sib. Fed. Univ. Chem. - 2017, DOI 10.17516/1998-2836-0031. - Библиогр.: 19 . - ISSN 1998-2836. - ISSN 2313-6049
   Перевод заглавия: Study of mobile oxygen in ordered/disordered nonstoichiometric Sr-Gd-cobaltate by simultaneous thermal analysis
Кл.слова (ненормированные):
разупорядоченный перовскит -- кобальтат -- ДСК -- ТГ -- кристаллическая структура -- подвижный кислород -- disordered perovskite -- cobaltate -- DSC -- TG -- crystal structure -- mobile oxygen
Аннотация: Методом синхронного термического анализа (ДСК/ТГ/масс-спектрометрия) при переменном парциальном давлении кислорода изучены разупорядоченная кубическая и упорядоченная по А-позициям тетрагональная фазы Sr-Gd-кобальтата (Sr/Gd=4). Показано, что упорядочение А-катионов приводит к снижению энтальпии отщепления О2, преимущественной локализации образовавшейся вакансии в одной из четырёх неэквивалентных позиций аниона О2- и снижению количества подвижного кислорода, удаляемого при изменении парциального давления О2. Наблюдаемые различия в свойствах мобильного кислорода и каталитической активности в реакции глубокого окисления метана для упорядоченной/разупорядоченной фазы перовскита обсуждены с позиций изменения доли анионов О2- с различным локальным окружением, содержащим от 0 до 4 катионов гадолиния.
Simultaneous thermal analysis (DSC/TG/mass-spectroscopy) under variable pressure was applied to study properties of mobile oxygen in cubic disordered and tetragonal A-site ordered Sr-Gd-cobaltate (Sr/Gd=4). It was shown that A-site cation ordering results in a decrease of an enthalpy of oxygen elimination, predominant localization of created anion vacancies only at one of four unequivalent crystallographic O-sites and depletion of amount of mobile oxygen, which can be removed at a reduced pressure. The observed properties of mobile oxygen and catalytic activity in reaction of methane deep oxidation for ordered/disordered perovskite phases are discussed in connection with a local environment of O2- crystallographic sites with a different number of Gd3+ cations nearby.

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Держатели документа:
RAS, SB, Inst Chem & Chem Technol, FRC Krasnoyarsk Sci Ctr, 50-24 Akad Gorodok, Krasnoyarsk 660036, Russia.
RAS, SB, Kirensky Inst Phys, 50-38 Akad Gorodok, Krasnoyarsk 660036, Russia.

Доп.точки доступа:
Дудников, Вячеслав Анатольевич; Dudnikov, V. A.; Соловьев, Леонид Александрович

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