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Raman investigation of fibrous zeolites of the natrolite group at high pressures of an aqueous medium / S. V. Goryainov [et al.] // Bull. Russ. Acad. Sci.: Phys. - 2012. - Vol. 76, Is. 7. - P. 804-807, DOI 10.3103/S1062873812070143. - Cited References: 7 . - ISSN 1062-8738
Кл.слова (ненормированные):
Aqueous medium -- High pressure -- Intermediate phase -- Intermediate phasis -- Raman bands -- Raman investigations -- Water molecule -- XRD -- Raman spectroscopy -- Silicon -- Zeolites
Аннотация: The intermediate phases preceding overhydration are observed by Raman spectroscopy both in scolecite Ca[Al2Si3O10] вЂў 3H2O and in thomsonite NaCa2[Al5Si 5O20] вЂў 6H2O upon compression in an aque-ous medium. The first intermediate phase of scolecite is attributed to a phase precursor revealed earlier using XRD at pressure of ~1 GPa. The widening of the Raman bands of O-H vibrations caused by the disordering of H 2O, which appears after additional water molecules are embedded in the zeolite channels, is typical of this intermediate phase. It is assumed on the basis of the Raman spectroscopy data that scolecite contains sec-ond overhydrated and second intermediate phases. В© 2012 Allerton Press, Inc.

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Публикация на русском языке Исследование методом КР волокнистых цеолитов группы натролита при высоких давлениях водной среды [Текст] / С. В. Горяйнов [и др.] // Изв. РАН. Сер. физич. - 2012. - Т. 76 № 7. - С. 895-898

Держатели документа:
Sobolev Institute of Geology and Mineralogy, Siberian Branch, Russian Academy of Sciences, Novosibirsk, 630090, Russian Federation
Novosibirsk State University, Novosibirsk, 630090, Russian Federation
Kirenskii Institute of Physics, Siberian Branch, Russian Academy of Sciences, Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Goryainov, S. V.; Krylov, A. S.; Крылов, Александр Сергеевич; Likhacheva, A.Yu.; Vtyurin, A. N.; Втюрин, Александр Николаевич
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    Low-temperature synthesis and structural properties of ferroelectric K 3WO3F3 elpasolite / V. V. Atuchin [et al.] // Chem. Phys. Lett. - 2010. - Vol. 493, Is. 1-3. - P. 83-86, DOI 10.1016/j.cplett.2010.05.023. - Cited References: 37 . - ISSN 0009-2614
Рубрики:
PEROVSKITE-LIKE OXYFLUORIDES
   CORE-LEVEL SPECTROSCOPY
   PHASE-TRANSITIONS
   SOLID-STATE
   ELECTRON-DIFFRACTION
   DIFFUSE-SCATTERING
   RHEED ANALYSIS
   POLAR
   BEHAVIOR
   (NH4)(3)TIOF5
Кл.слова (ненормированные):
Chemical synthesis -- Elpasolite -- Ferroelectric phase transition -- Fluorine atoms -- Low temperature synthesis -- Low temperatures -- Oxyfluorides -- Partial ordering -- Room temperature -- SEM -- Space Groups -- Structure parameter -- XRD -- Chemical properties -- Ferroelectric materials -- Ferroelectricity -- Fluorine -- Oxygen -- Phase transitions -- Rietveld method -- Single crystals -- Synthesis (chemical) -- X ray photoelectron spectroscopy -- X ray powder diffraction -- Scanning electron microscopy
Аннотация: Low-temperature ferroelectric G2 polymorph of K3WO 3F3 has been prepared by chemical synthesis. Structural and chemical properties of the final product have been evaluated with X-ray powder diffraction (XRD), scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). Structure parameters of G2-K 3WO3F3 are refined by the Rietveld method from XRD data measured at room temperature (space group Cm, Z = 2, a = 8.7350(3), b = 8.6808(5), c = 6.1581(3), ? = 135.124(3), V = 329.46(3) 3; RB = 2.47%). Partial ordering of oxygen and fluorine atoms has been found over anion positions. Mechanism of ferroelectric phase transition in A2BMO3F3 oxyfluorides is discussed. В© 2010 Elsevier B.V. All rights reserved.

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Держатели документа:
Laboratory of Optical Materials and Structures, Institute of Semiconductor Physics, SB RAS, Novosibirsk 630090, Russian Federation
Laboratory of Nanolithography and Nanodiagnostics, Institute of Semiconductor Physics, SB RAS, Novosibirsk 630090, Russian Federation
Laboratory of Physical Principles for Integrated Microelectronics, Institute of Semiconductor Physics, SB RAS, Novosibirsk 630090, Russian Federation
Laboratory of Crystal Physics, Institute of Physics, SB RAS, Krasnoyarsk 660036, Russian Federation

Доп.точки доступа:
Atuchin, V. V.; Gavrilova, T. A.; Kesler, V. G.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Aleksandrov, K. S.; Александров, Кирилл Сергеевич
}
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Microwave sol–gel synthesis and upconversion photoluminescence properties of CaGd2(WO4)4:Er3+/Yb3+ phosphors with incommensurately modulated structure / C. S. Lim [et al.] // J. Solid State Chem. - 2015. - Vol. 228. - P. 160-166, DOI 10.1016/j.jssc.2015.04.032. - Cited References:70. - This study was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT & Future Planning (2014-046024). VVA, ASA and ASO are partially supported by the Ministry of Education and Science of the Russian Federation. . - ISSN 0022. - ISSN 1095-726X. -

РУБ Chemistry, Inorganic & Nuclear + Chemistry, Physical
Рубрики:
CORE-LEVEL SPECTROSCOPY
LUMINESCENCE PROPERTIES
WHITE-LIGHT
Кл.слова (ненормированные):
Double tungstate -- Microwave sol-gel -- Upconversion -- XRD refinement -- Raman
Аннотация: CaGd2−x(WO4)4:Er3+/Yb3+ phosphors with the doping concentrations of Er3+ and Yb3+ (x=Er3++Yb3+, Er3+=0.05, 0.1, 0.2 and Yb3+=0.2, 0.45) have been successfully synthesized by the microwave sol–gel method. The crystal structure of CaGd2−x(WO4)4:Er3+/Yb3+ tungstates have been refined, and upconversion photoluminescence properties have been investigated. The synthesized particles, being formed after the heat-treatment at 900 °C for 16 h, showed a well crystallized morphology. Under the excitation at 980 nm, CaGd2(WO4)4:Er3+/Yb3+ particles exhibited a strong 525-nm and a weak 550-nm emission bands in the green region and a very weak 655-nm emission band in the red region. The Raman spectrum of undoped CaGd2(WO4)4 revealed about 12 narrow lines. The strongest band observed at 903 cm−1 was assigned to the ν1 symmetric stretching vibration of WO4 tetrahedrons. The spectra of the samples doped with Er and Yb obtained under the 514.5 nm excitation were dominated by Er3+ luminescence preventing the recording of these samples Raman spectra. Concentration quenching of the erbium luminescence at 2H11/2→4I15/2 transition is weak in the range of erbium doping level xEr=0.05–0.2, while, for transition 4S3/2→4I15/2, the signs of concentration quenching become pronounced at xEr=0.2.

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Держатели документа:
Hanseo Univ, Dept Adv Mat Sci & Engn, Seosan 356706, South Korea.
SB RAS, LV Kirensky Phys Inst, Lab Coherent Opt, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Dept Photon & Laser Technol, Krasnoyarsk 660079, Russia.
SB RAS, LV Kirensky Phys Inst, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
SB RAS, LV Kirensky Phys Inst, Lab Mol Spect, Krasnoyarsk 660036, Russia.
SB RAS, Inst Semicond Phys, Lab Opt Mat & Struct, Novosibirsk 630090, Russia.
Tomsk State Univ, Funct Elect Lab, Tomsk 634050, Russia.
Novosibirsk State Univ, Lab Semicond & Dielect Mat, Novosibirsk 630090, Russia.

Доп.точки доступа:
Lim, Chang Sung; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Atuchin, V. V.; Атучин, Виктор Валерьевич
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    Preparation of NaSrLa(WO4)3:Ho3+/Yb3+ ternary tungstates and their upconversion photoluminescence properties / C. S. Lim [et al.] // Mater. Lett. - 2016. - Vol. 181. - P. 38-41, DOI 10.1016/j.matlet.2016.05.121. - Cited References: 24. - This research was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (2015-058813), SB RAS Program No.II.2P (No. 0358-2015-0012) and Russian Foundation for Basic Research (15-52-53080). . - ISSN 0167-577X
   Перевод заглавия: Синтез тройных вольфраматов NaSrLa1-x(WO4)3:Ho3+/Yb3+ и их апконверсионные люминесцентные свойства

РУБ Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
VIBRATIONAL PROPERTIES
   LUMINESCENCE PROPERTIES
   MODULATED STRUCTURE
   PHOSPHORS
   CRYSTAL
   RED
Кл.слова (ненормированные):
Tungstate -- Phosphor -- Sol-gel preparation -- Luminescence -- Raman spectroscopy -- XRD
Аннотация: NaSrLa1-x(WO4)3:Ho3+/Yb3+ ternary tungstates were synthesized via microwave sol-gel route. Well-crystallized particles with particle sizes of 2-5 ?m were obtained after heat-treatment at 900 °C for 16 h. Under the excitation at 980 nm, the particles showed yellow emissions based on the strong 545 and 655 nm emission bands. The preferable Yb3+:Ho3+ ratio was obtained to be 9:1. Raman spectra of the doped particles indicated the presence of strong Ho3+ luminescence lines. The pump power dependence and Commission Internationale de L'Eclairage chromaticity of the upconversion emission intensity were evaluated. © 2016 Published by Elsevier B.V.

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Держатели документа:
Department of Advanced Materials Science and Engineering, Hanseo University, Seosan, South Korea
Laboratory of Optical Materials and Structures, Institute of Semiconductor Physics, SB RAS, Novosibirsk, Russian Federation
Functional Electronics Laboratory, Tomsk State University, Tomsk, Russian Federation
Laboratory of Semiconductor and Dielectric Materials, Novosibirsk State University, Novosibirsk, Russian Federation
Laboratory of Coherent Optics, Kirensky Institute of Physics, SB RAS, Krasnoyarsk, Russian Federation
Laboratory of Crystal Physics, Kirensky Institute of Physics, SB RAS, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation

Доп.точки доступа:
Lim, C. S.; Atuchin, V. V.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Molokeev, M. S.; Молокеев, Максим Сергеевич
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Heat capacity, p-T phase diagram, and structure of Rb2KTiOF5 / V. . Fokina [et al.] // Phys. Solid State. - 2008. - Vol. 50, Is. 11. - P. 2175-2183, DOI 10.1134/S1063783408110280. - Cited References: 23. - This work was supported by the Russian Foundation for Basic Research, project no. 06-02-16102. . - ISSN 1063-7834

РУБ Physics, Condensed Matter
Рубрики:
ELECTRON-DIFFRACTION
   TRANSITIONS
   OXYFLUORIDES
   (NH4)(2)KWO3F3
   TEMPERATURE
   XRD
   CS
Кл.слова (ненормированные):
61 -- 50 -- Ks -- 65 -- 40 -- Ba -- 65 -- 40 -- gd -- 78 -- 30 -- Hv -- 81 -- 30 -- Dz
Аннотация: Elpasolite Rb2KTiOF5 (space group, Fm was synthesized using a solid-phase reaction method. The temperature dependences of the heat capacity, the unit cell parameters, the structure, the permittivity, the response to an external pressure, and the Raman spectra were studied. A nonferroelectric phase transition was revealed at T (0) = 215 K; the transition is accompanied by a tetragonal distortion of the unit cell (space group I4/m, Z = 10) and a change in the entropy (S (0) = Rln8), which is anomalously large for perovskite-like oxyfluorides with atomic cations. The specific features of the mechanism of structure distortion are discussed in combination with the previous experimental data obtained for cryolite (NH4)(3)TiOF5 and elpasolite Rb2KGaF6.

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Держатели документа:
Kirensky Institute of Physics, Siberian Branch, Russian Academy of Sciences, Akademgorodok, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, pr. Svobodnyi 59, Krasnoyarsk, 660074, Russian Federation
Institute of Chemistry, Far East Division, Russian Academy of Sciences, pr. Stoletiya Vladivostoka 159, Vladivostok, 690022, Russian Federation

Доп.точки доступа:
Fokina, V. D.; Фокина, Валентина Дмитриевна; Flerov, I. N.; Флёров, Игорь Николаевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Pogoreltsev, E. I.; Погорельцев, Евгений Ильич; Bogdanov, E. V.; Богданов, Евгений Витальевич; Krylov, A. S.; Крылов, Александр Сергеевич; Bovina, A. F.; Бовина, Ася Федоровна; Voronov, V. N.; Воронов, Владимир Николаевич; Laptash, N. M.
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Charge ordering in Mn2BO4: XRD and XANES studies / N. V. Kazak [et al.] // VI Euro-Asian Symposium "Trends in MAGnetism" (EASTMAG-2016) : abstracts / ed.: O. A. Maksimova, R. D. Ivantsov. - Krasnoyarsk : KIP RAS SB, 2016. - Ст. I10.6. - P. 432. - References: 3. - This work has been financed by the Council for Grants of the President of the Russian Federation (SP-938.2015.5), the RFBR (№ 16-32-60049 mol_a_dk, № 16-32-00206 mol_a), SB RAS program № II.2P contract 0358-2015-0005 and by «UMNIK» program. . - ISBN 978-5-904603-06-9
Кл.слова (ненормированные):
charge ordering -- x-ray spectroscopy -- x-ray diffraction -- phase transitions

Доп.точки доступа:
Kazak, N. V.; Казак, Наталья Валерьевна; Platunov, M. S.; Платунов, Михаил Сергеевич; Knyazev, Yu. V.; Князев, Юрий Владимирович; Bezmaternykh, L. N.; Безматерных, Леонард Николаевич; Veligzhanin, A. A.; Велигжанин А. А.; Zubavichus, Y. V.; Зубавичус Я. В.; Trigub, A.; Тригуб А.; Solovyov, L. A.; Соловьев, Леонид Александрович; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич; Euro-Asian Symposium "Trends in MAGnetism"(6 ; 2016 ; Aug. ; 15-19 ; Krasnoyarsk); "Trends in MAGnetism", Euro-Asian Symposium(6 ; 2016 ; Aug. ; 15-19 ; Krasnoyarsk); Институт физики им. Л.В. Киренского Сибирского отделения РАН

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    Incommensurately modulated structure and spectroscopic properties of CaGd2(MoO4)4:Ho3+/Yb3+ phosphors for up-conversion applications / C. S. Lim [et al.] // J. Alloys Compd. - 2017. - Vol. 695. - P. 737-746, DOI 10.1016/j.jallcom.2016.06.134. - Cited References: 60. - This research was supported by the Basic Science Research Program through the National Research Foundation of Korea funded by the Ministry of Education (2015-058813) and the Russian Foundation for Basic Research (15-52-53080). VVA, ASA and ASO were partially supported by the Ministry of Education and Science of the Russian Federation. . - ISSN 0925-8388
   Перевод заглавия: Несоразмерно модулированная структура и спектроскопические свойства люминофоров CaGd2(MoO4)4:Ho3+/Yb3+ для апконверсионного применения
Кл.слова (ненормированные):
Modulation -- Molybdate -- Raman -- Sol-gel synthesis -- Upconversion -- XRD
Аннотация: CaGd2(MoO4)4:Ho3+/Yb3+ phosphors doped by Ho3+ and Yb3+ (Ho3+ = 0 and 0.05, and Yb3+ = 0, 0.35, 0.40, 0.45 and 0.50) were successfully synthesized by the microwave sol-gel method. The synthesized particles, being formed after heat-treatment at 900 °C for 16 h, showed a well crystallized morphology. All compounds are (3 + 2)D incommensurately modulated with superspace group I41/a(α,β,0)00(-β,α,0)00. It was found that parameter (α2 + β2)1/2 is proportional to cell parameter a for all studied compositions and, therefore, modulation vector k is the same for all known CaRE2(MoO4)4 compounds. The modulation vector invariance is a specific and valuable feature of this type of the structure. Under the excitation at 980 nm, the doped particles exhibited the yellow emission composed of green (545-nm) and red (655-nm) emission bands due to frequency upconversion (UC). The pump power dependence and CIE chromaticity of the UC emission were evaluated. The shape of UC bands in CaGd2(MoO4)4:Ho3+/Yb3+ is dependent on the Yb content due to the influence of the crystal field affecting a holmium ion. 13 Raman-active modes of the CaGd2(MoO4)4 lattice were identified via a comparison of experimental Raman spectra and the lattice dynamics simulation results. Four additional Raman lines were found in the region of stretching vibrations and, at least, two additional modes are present in the bending mode region. These additional modes are ascribed to incommensurate crystal lattice modulation. Luminescence bands of Ho ions are severely broadened due to a statistical disorder in the CaGd2−xYby (MoO4)4 lattice.

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Держатели документа:
Department of Advanced Materials Science & Engineering, Hanseo University, Seosan, South Korea
Laboratory of Optical Materials and Structures, Institute of Semiconductor Physics, SB RAS, Novosibirsk, Russian Federation
Functional Electronics Laboratory, Tomsk State University, Tomsk, Russian Federation
Laboratory of Semiconductor and Dielectric Materials, Novosibirsk State University, Novosibirsk, Russian Federation
Institute of Chemistry, Tyumen State University, Tyumen, Russian Federation
Laboratory for Nonlinear Optics and Spectroscopy, Siberian Federal University, Krasnoyarsk, Russian Federation
Laboratory of Coherent Optics, Kirensky Institute of Physics, SB RAS, Krasnoyarsk, Russian Federation
Laboratory of Crystal Physics, Kirensky Institute of Physics, SB RAS, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation
Laboratory of Molecular Spectroscopy, Kirensky Institute of Physics, SB RAS, Krasnoyarsk, Russian Federation
Department of Photonics and Laser Technologies, Siberian Federal University, Krasnoyarsk, Russian Federation

Доп.точки доступа:
Lim, C. S.; Atuchin, V. V.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич
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    Верещагин, С. Н.
    Изучение фазового перехода порядок-беспорядок в нестехиометрическом Sr-Gd-кобальтате методами ДСК, ТГ и РСА / С. Н. Верещагин, В. А. Дудников, Л. А. Соловьев // Журн. СФУ. Сер. "Химия". - 2016. - Т. 9, № 3. - С. 326-336 ; J. Sib. Fed. Univ. Chem., DOI 10.17516/1998-2836-2016-9-3-326-336. - Библиогр.: 26. - Исследование выполнено при финансовой поддержке Российского фонда фундаментальных исследований, Правительства Красноярского края, Красноярского краевого фонда поддержки научной и научно-технической деятельности в рамках научного проекта 16-43-240505 «р_а». . - ISSN 1998-2836. - ISSN 2313-6049
   Перевод заглавия: DSC+TG and XRD study of order-disorder transition in nonstoichiometric Sr-Gd-cobaltate
Рубрики:
PEROVSKITE-TYPE OXIDES
   PHASE-TRANSITION
   OXYGEN SORPTION
   PERFORMANCE
Кл.слова (ненормированные):
perovskite -- order-disorder -- phase transition -- DSC -- перовскит -- порядок-беспорядок -- фазовый переход -- ДСК
Аннотация: Методами термического и рентгеноструктурного анализа в интервале температур 11001473 К изучен процесс взаимопревращения тетрагонального перовскита Sr ( 0.8 ) Gd ( 0.2 ) CoO ( 3-d ) с упорядоченным расположением катионов Sr/Gd и анионных вакансий в кубическую разупорядоченную модификацию. Показано, что фазовое превращение протекает как размытый фазовый переход первого рода. Процесс разупорядочения не зависит от скорости нагрева и контролируется термодинамическими характеристиками процессов в кристалле, тогда как процесс образования упорядоченной тетрагональной структуры контролируется кинетическими факторами. Проведен количественный анализ температурной зависимости теплоемкости на основе размытых фазовых переходов.
Process of interconversion of tetragonal Sr(0.8) Gd(0.2) CoO(3-d) (with ordered Sr/Gd cations and anion vacancies) to cubic one (with disordered structure) was studied by X-ray structural and thermal analysis at 1100-1473 K. It was shown that the transformation is a first order diffuse phase transition. The ramp rate does not affect cation and anion vacancies disordering which is controlled by thermodynamic parameters of the processes in the solid whereas cubic to tetragonal transition is kinetically controlled. A theory of diffuse phase transition was applied to quantitatively analyze heat capacity temperature dependence.

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Держатели документа:
Институт химии и химической технологии СО РАН
Институт физики им. Л. В. Киренского СО РАН

Доп.точки доступа:
Дудников, Вячеслав Анатольевич; Dudnikov, V. A.; Соловьев, Леонид Александрович; Solovyov L. A.; Vereshchagin S. N.

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The Raman spectroscopy, XRD, SEM, and AFM study of arabinogalactan sulfates obtained using sulfamic acid / B. N. Kuznetsov [et al.] // Russ. J. Bioorgan. Chem. - 2017. - Vol. 43, No. 7. - P. 32-36, DOI 10.1134/S106816201707010X. - Cited References: 9. - The work was financially supported by the Russian Foundation for Basic Research and the Government of the Krasnoyarsk krai (project no. 16-43-242083). . - ISSN 1068-1620
Кл.слова (ненормированные):
physicochemical investigation -- sulfated arabinogalactan -- «green» synthesis -- sulfamic acid -- urea
Аннотация: The structure of sodium salts of sulfated arabinogalactan (AG), obtained by sulfation of larch wood AG with sulfamic acid – urea mixture in the medium of 1,4-dioxane was investigated with the use of Raman spectroscopy, X-ray diffraction (XRD), scaning electron microscopy (SEM) and aromatic force microscopy (AFM) methods. The introduction of sulfate groups into the structure of AG was confirmed by appearance in Raman spectra new absorption bands characteristic for the deformation vibrations of d (SO3) at 420 cm-1 and d (O=S=O) at 588 cm-1, stretching vibrations n (C–O–S) at 822 cm-1, symmetric stretching vibrations ns (O=S=O) at 1076 cm-1, asymmetric stretching vibrations nas (О=S=O) at 1269 cm-1. According to XRD data the amorphization of arabinogalactan structure take place during it`s sulfation. The difference in the morphology of initial and sulfated arabinogalactans was established by SEM method. Initial arabinigalactan consists of particles of globular shape with size of 10–90 µm, but sulfates of AG – from particles of different shapes and sizes of 1–8 µm. According to AFM data the surface of film of arabinogalactan sulfates is formed by the rather homogeneous spherical particles with sizes near 70 nm. The mean-square value of the surface rounghness is equal to 33 nm.

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Публикация на русском языке Исследование методами КР, РФА, РЭМ и АСМ сульфатов арабиногалактана, полученных с использованием сульфаминовой кислоты [Текст] / Б. Н. Кузнецов [и др.] // Хим. растит. сырья. - 2016. - № 4. - С. 43-48

Держатели документа:
Институт химии и химической технологии СО РАН
Сибирский федеральный университет
Институт физики им. Л. В. Киренского СО РАН

Доп.точки доступа:
Kuznetsov, B. N.; Vasil'eva, N. Yu.; Levdansky, A. V.; Karacharov, A. A.; Krylov, A. S.; Крылов, Александр Сергеевич; Mazurova, E. V.; Bondarenko, G. N.; Levdansky, V. A.; Kazachenko, A. S.
}
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10.

Study of mixed-valence Mn2BO4 using XRD, XPS and XAFS spectroscopies / N. V. Kazak [et al.] // Physica B. - 2019. - Vol. 560. - P. 228-235, DOI 10.1016/j.physb.2019.02.019. - Cited References: 39. - This work has been financed by Russian Foundation for Basic Research (17-02-00826 and 16-32-60049 grant numbers). . - ISSN 0921-4526. - ISSN 1873-2135

РУБ Physics, Condensed Matter
Рубрики:
SPIN-GLASS BEHAVIOR
MAGNETIC-PROPERTIES
PROFILE REFINEMENT
Кл.слова (ненормированные):
Charge-ordering -- Mixed-valence -- XAS -- XRD -- XPS
Аннотация: The valence states and local structure around Mn atoms in mixed-valence Mn2BO4 have been studied by temperature dependent X-ray powder diffraction (XRPD), X-ray photoelectron (XPS) and Mn K-edge X-ray absorption (XAFS) spectroscopies measurements. X-ray absorption near-edge structure (XANES) and XPS have been used to measure the average oxidation state of Mn in bulk and near-surface of the material. The edge position, peak shapes and pre-edge features of Mn K-edge XANES spectra have been discussed. The pronounced temperature dependence of the Debye-Waller (DW) factor corresponding to the MnO coordination shell has been found from the extended x-ray absorption fine structure (EXAFS) analysis and has been associated with variations in the local distortions in MnO6 octahedra and emergence of short-range magnetic correlations at low temperatures. The XRPD measurements have been carried out at 298, 523 and 773 K. The monoclinic symmetry (P21/n) was found to persist up to highest temperature measured. The BVS calculations have revealed large valence difference between two manganese sites that strongly supports the presence of charge ordering up to high temperatures.

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Держатели документа:
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.
Fed Res Ctr KSC SB RAS, Inst Chem & Chem Technol, Krasnoyarsk 660036, Russia.
Natl Res Ctr, Kurchatov Inst, Moscow 123182, Russia.

Доп.точки доступа:
Kazak, N. V.; Казак, Наталья Валерьевна; Platunov, M. S.; Платунов, Михаил Сергеевич; Knyazev, Yu. V.; Князев, Юрий Владимирович; Moshkina, E. M.; Мошкина, Евгения Михайловна; Solovyov, L. A.; Vereshchagin, S. N.; Mikhlin, Yu. L.; Veligzhanin, A. A.; Trigub, A. L.; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич; Russian Foundation for Basic Research [17-02-00826, 16-32-60049]
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11.

    Состав, структура и реакционная способность при восстановлении водородом композиционных материалов системы α-Fe2O3–CaFe2O4 / В. В. Юмашев [и др.] // Журнал СФУ. Химия. - 2019. - Т. 12, Вып. 1. - С. 54-72 ; J. Sib. Fed. Univ. Chem., DOI 10.17516/1998-2836-0108. - Библиогр.: 37 . - ISSN 1998-2836. - ISSN 2313-6049
   Перевод заглавия: Composition, Structure and Reduction Reactivity of Composite Materials of the α-Fe2O3-CaFe2O4 System by Hydrogen

РУБ Chemistry, Multidisciplinary
Рубрики:
CHEMICAL LOOPING GASIFICATION
OXYGEN CARRIER
PARTIAL OXIDATION
Кл.слова (ненормированные):
твердофазный синтез -- феррит кальция -- РФА -- СЭМ-ЭДС -- термопрограммируемое восстановление водородом -- solid-phase synthesis -- calcium ferrite -- XRD -- SEM-EDS -- temperature-programmed reduction by hydrogen
Аннотация: В работе изучены композиционные материалы системы α-Fe2O3-CaFe2O4, полученные методом высокотемпературного твердофазного синтеза из оксидов Са и Fe(III) с вариацией мольного отношения СаО/Fe2O3 от 0.15 до 1.00. Материалы охарактеризованы методами рентгеновской дифракции (РФА), сканирующей электронной микроскопии с системой энергодисперсионного микроанализа (СЭМ-ЭДС) и синхронного термического анализа (СТА) в режиме термопрограммируемого восстановления водородом (H2-ТПВ). СЭМ-ЭДС - исследование образцов выявило формирование сложной микроструктуры материала по типу «ядро-оболочка» с фазой гематита в качестве «ядра». H2-ТПВ образцов позволило установить, что с увеличением содержания фазы CaFe2O4 (от 33.4 до 97.5 мас. %) наблюдается снижение вклада низкотемпературных форм решеточного кислорода в областях 350-510 °С (до 2.6 раза) и 510-650 °С (до 1.7 раза) и рост вклада высокотемпературной формы кислорода в интервале 650-900 °С (до 2 раз). На основе оценки подвижности решеточного кислорода высказано предположение о перспективности использования полученных композиционных материалов с содержанием фазы CaFe2O4 более 55.2 мас. % в качестве носителей кислорода в химических циклических процессах получения синтез-газа.
In this paper, α-Fe2O3–CaFe2O4 composite materials obtained by high-temperature solid-phase synthesis from Ca and Fe (III) oxides with varying molar ratio CaO/Fe2O3 in the range 0.15-1.00 were investigated. The materials are characterized by Х-ray diffraction (XRD), scanning electron microscopy with energy-dispersive X-ray microanalysis (SEM-EDS) and simultaneous thermal analysis (STA) in the hydrogen temperature-programmed reduction mode (H2-TPR). SEM-EDS studies of the specimens were revealed a formation of the “core-shell” type complex microstructure of material with the hematite phase as the “core”. H2-TPR of the specimens allowed to establish a decrease of the contribution of low-temperature forms of lattice oxygen in areas of 350-510 °С (up to 2.6 times) and 510-650 °С (up to 1.7 times), and the growth of the contribution of the high-temperature oxygen form in the range of 650-900 °С (up to 2 times) with an increase in the content of the phase CaFe2O4 from 33.4 to 97.5 wt. %. Relying on the assessment of lattice oxygen mobility, it was suggested, that the samples with content of CaFe2O4 phase more than 55.4 wt. % are promising for use as oxygen carriers in chemical looping processes of syngas production.

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

Доп.точки доступа:
Юмашев, Владимир Витальевич; Yumashev, Vladimir V.; Кирик, Надежда Павловна; Kirik N. P.; Шишкина, Нина Николаевна; Shishkina, Nina N.; Князев, Юрий Владимирович; Knyazev, Yu. V.; Жижаев, Анатолий Михайлович; Zhyzhaev, A. M.; Соловьев, Леонид Александрович; Solov'ev, L. A.

}
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12.

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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13.

Solid-phase transformation of Cs+- and Sr2+-bearing zeolite sorbents derived from cenospheres to mineral-like forms / S. N. Vereshchagin [et al.] // Materials Research Society Symposium Proceedings. - 2009. - Vol. 1193: 32nd Symposium on Scientific Basis for Nuclear Waste Management (24 May 2009 through 29 May 2009, St. Petersburg, ) Conference code: 79940. - P87-94 . - ISBN 02729172 (ISSN); 9781605111667 (ISBN)
Кл.слова (ненормированные):
Apparent activation energy -- Cenospheres -- Crystalline minerals -- Crystalline phasis -- Crystallization temperature -- Higher temperatures -- Long-term disposal -- Multi phase systems -- Pollucites -- Principal Components -- Solid-phase transformation -- Temperature range -- Thermal treatment -- Thermochemical transformations -- Transformation temperatures -- XRD analysis -- Activation energy -- Atmospheric pressure -- Cesium -- Crystalline materials -- Crystallization -- Fly ash -- Metallic glass -- Radioactive waste disposal -- Radioactive wastes -- Silicate minerals -- Sodium -- Sorbents -- Sorption -- Strontium -- Synthesis (chemical) -- Waste management -- Atmospheric temperature
Аннотация: The paper describes the studies of the transformation of Cs+- and Sr2+-containing zeolite sorbents synthesized from fly ash cenospheres to crystalline mineral composition, suitable for the long-term disposal. Series of Cs+- and Sr2+-exchanged NaP1-containing sorbents were subjected to the thermochemical transformation in the temperature range 40-1100°C at atmospheric pressure in air and the progress of reaction was monitored by DSC and XRD analysis. It was shown that initial sodium zeolite undergoes two-step transformation at 736-785°C and 892-982°C forming nepheline as the principle product, with the conversion temperatures being dependant on the heating rate. The thermal treatment of Cs+-bearing zeolite sorbent led to formation of a complex multiphase system, the principal components of which were nepheline and pollucite. Increasing cesium content in the samples led to a monotonous shift of crystallization peak to the higher temperature range (1005-1006°C). A more complicated behavior was observed for Sr2+-containing samples, for which the crystallization temperature tends to increase (compared with NaP1) at lower Sr contents, but it starts decreasing parallel to the Sr2+ content at Sr2+ loadings 10 mg/g. The principal crystalline phases in Sr-NaP1 sample conversion were nepheline and Sr2+- containing feldspar, the quantity of which increased parallel to the increase of strontium content in zeolite. Apparent activation energies of thermochemical transformations were calculated and possible approaches to reduce transformation temperature are discussed and experimentally illustrated. © 2009 Materials Research Society.

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Держатели документа:
Institute of Chemistry and Chemical Technology SB RAS, 42 K. Marx Street, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, 79 Svobodnyi Avenue, Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Vereshchagin, S.N.; Vereshchagina, T.A.; Solovyov, L.A.; Shishkina, N.N.; Vasilieva, N.G.; Anshits, A.G.
}
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14.

    Kinetics and mechanism of BaLaCuS3 oxidation / N. O. Azarapin, N. A. Khritokhin, V. V. Atuchin [et al.] // Crystals. - 2023. - Vol. 13, Is. 6. - Ст. 903, DOI 10.3390/cryst13060903. - Cited References: 65. - The work was partially carried out using the resources of the Research Resource Center “Natural Resources Management and Physico-Chemical Research” (Tyumen University) with financial support from the Ministry of Science and Higher Education of the Russian Federation (contract No. 05.594.21.0019., Unique identification number RFMEFI59420X0019). M.S. Molokeev was supported by the Tyumen Oblast Government, as part of the West-Siberian Interregional Science and Education Center’s project No. 89-DON (3). - The authors would like to thank the staff of the Engineering Center of the Tyumen State University (special Alexej V. Matigorov) for their help in carrying out physical and chemical tests . - ISSN 2073-4352
   Перевод заглавия: Кинетика и механизм окисления BaLaCuS3
Кл.слова (ненормированные):
BaLaCuS3 -- complex sulfide -- oxidation -- kinetic -- XRD analysis
Аннотация: The oxidation reactions of BaLaCuS3 in the artificial air atmosphere were studied at different heating rates in the temperature range of 50–1200 °C. The oxidation stages were determined by DSC-TG, XRD and IR–vis methods. The kinetic characteristics of the proceeding reactions were obtained with the use of the Kissinger model in a linearized form. Compound BaLaCuS3 was stable in the air up to 280 °C. Upon further heating up to 1200 °C, this complex sulfide underwent three main oxidation stages. The first stage is the formation of BaSO4 and CuLaS2. The second stage is the oxidation of CuLaS2 to La2O2SO4 and copper oxides. The third stage is the destruction of La2O2SO4. The final result of the high-temperature treatment in the artificial air atmosphere was a mixture of barium sulfate, copper (II) oxide and La2CuO4. The mechanism and stages of BaLaCuS3 oxidation and further interactions of the components were discussed.

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Держатели документа:
Department of Inorganic and Physical Chemistry, Tyumen State University, Tyumen 625003, Russia
Laboratory of Optical Materials and Structures, Institute of Semiconductor Physics, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090, Russia
Research and Development Department, Kemerovo State University, Kemerovo 650000, Russia
Department of Industrial Machinery Design, Novosibirsk State Technical University, Novosibirsk 630073, Russia
R&D Center “Advanced Electronic Technologies”, Tomsk State University, Tomsk 634034, Russia
Laboratory for Nanomaterials and Nanoelectronics, Center for Nature-Inspired Engineering, Technology Park, Tyumen State University, Tyumen 625003, Russia
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk 660036, Russia
Laboratory of Theory and Optimization of Chemical and Technological Processes, University of Tyumen, Tyumen 625003, Russia
Institute of Engineering Physics and Radioelectronics, Siberian Federal University, Krasnoyarsk 660041, Russia
Hybrid Nanodevice Research Group (HNRG), Department of Electrical Engineering, Indian Institute of Technology Indore, Indore 453552, India
Centre for Advanced Electronics (CAE), Indian Institute of Technology Indore, Indore 453552, India
School of Engineering, RMIT University, Melbourne, VIC 3001, Australia
Institute of Solid State Chemistry, UB RAS, Yekaterinburg 620990, Russia

Доп.точки доступа:
Azarapin, N. O.; Khritokhin, N. A.; Atuchin, V. V.; Gubin, A. A.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Mukherjee, S.; Andreev, O. V.
}
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15.

The relationship between the structural characteristics of α-Fe2O3 catalysts and their lattice oxygen reactivity regarding hydrogen / N. Kirik, A. Krylov, A. Boronin [et al.] // Materials. - 2023. - Vol. 16, Is. 12 : The 15th Anniversary of Materials — Recent Advances in Catalytic Materials. - Ст. 4466, DOI 10.3390/ma16124466. - Cited References: 63. - This work was conducted within the framework of the budget project for the Institute of Chemistry and Chemical Technology of the Siberian Branch of the Russian Academy of Sciences, Federal Research Center KSC SB RAS, No. FWES–2021–0013 . - ISSN 1996-1944
Кл.слова (ненормированные):
α-Fe2O3 -- catalysts -- calcinations -- XRD -- XPS -- Raman spectroscopy characterization -- temperature-programmed reduction
Аннотация: In this paper, the relationship between the structural features of hematite samples calcined in the interval of 800–1100 °C and their reactivity regarding hydrogen studied in the temperature-programmed reaction (TPR-H2) was studied. The oxygen reactivity of the samples decreases with the increasing calcination temperature. The study of calcined hematite samples used X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), X-ray Photoelectron Spectroscopy (XPS), and Raman spectroscopy, and their textural characteristics were studied also. According to XRD results, hematite samples calcined in the temperature range under study are monophase, represented by the α-Fe2O3 phase, in which crystal density increases with increasing calcination temperature. The Raman spectroscopy results also register only the α-Fe2O3 phase; the samples consist of large, well-crystallized particles with smaller particles on their surface, having a significantly lower degree of crystallinity, and their proportion decreases with increasing calcination temperature. XPS results show the α-Fe2O3 surface enriched with Fe2+ ions, whose proportion increases with increasing calcination temperature, which leads to an increase in the lattice oxygen binding energy and a decrease in the α-Fe2O3 reactivity regarding hydrogen.

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Держатели документа:
Federal Research Center “Krasnoyarsk Science Center of Siberian Branch of the Russian Academy of Sciences”, Institute of Chemistry and Chemical Technology, 50/24, Akademgorodok, 660036 Krasnoyarsk, Russia
Federal Research Center “Krasnoyarsk Science Center of Siberian Branch of the Russian Academy of Sciences”, Kirensky Institute of Physics, 50/38, Akademgorodok, 660036 Krasnoyarsk, Russia
Federal Research Center Boreskov Institute of Catalysis, 5, Ac. Lavrentieva Ave., 630090 Novosibirsk, Russia
Department of Chemistry, 79, Svobodny Ave., Siberian Federal University, 660041 Krasnoyarsk, Russia

Доп.точки доступа:
Kirik, N.; Krylov, A. S.; Крылов, Александр Сергеевич; Boronin, A.; Koshcheev, S.; Solovyov, L.; Rabchevskii, E.; Shishkina, N.; Anshits, A.
}
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