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1.


   
    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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2.


   
    Применение процессного моделирования для интерпретации вариации стабильных изотопов в годичных кольцах деревьев / Н. Д. Васильева, С. Н. Софронова, В. В. Баринов [и др.] // Лесотехнич. журн. - 2023. - Т. 13, № 4, Ч. 2. - С. 23-38 ; Forest. Eng. J., DOI 10.34220/issn.2222-7962/2023.4/15. - Библиогр.: 33. - Исследование выполнено за счет гранта Российского научного фонда № 21-17-00006, (https://rscf.ru/en/project/21-17-00006/) . - ISSN 2222-7962
   Перевод заглавия: Application of process-based modelling for interpretation of stable isotope variations in tree rings
Кл.слова (ненормированные):
дендрохрогология -- стабильные изотопы -- моделирование -- углерод -- кислород -- водород -- dendrochronology -- stable isotopes -- modelling -- carbon -- oxygen -- hydrogen
Аннотация: Ширина годичных колец деревьев и изотопный состав стабильных изотопов углерода (δ13C), кислорода (δ18O) и водорода (δ2H) в целлюлозе годичных колец широко используются для реконструкций условий окружающей среды. Применение моделей, способных описать вариацию стабильных изотопов в годичных кольцах деревьев, представляет собой набор инструментов для интерпретации изменений окружающей среды на экофизиологическом уровне. В данной работе хронологии с погодичным временным разрешением, полученные по стабильным изотопам δ13С, δ18O и δ2H в целлюлозе годичных колец хвойных для региона Дельта реки Маккензи в Канаде (68° 30′ с.ш., 133° 48′ з.д.) для периода с 1901 по 2009 гг., были сопоставлены с модельными расчетами для интерпретации экофизиологического сигнала. При помощи процессной модели (LPX) нам удалось смоделировать δ13С вариацию, значимо коррелирующую с измеренными данными (r = 0.29; p = 0.002) для периода с 1901 по 2009 гг. Модельные расчеты по кислороду и водороду требуют дальнейшего преобразования модельных блоков, в частности, требуют доработки включения источника воды, используемой деревьями, блока оттаивания и промерзания почвы с учетом вечной мерзлоты, а также экспериментальных данных по содержанию δ18O и δ2H в воде.
Tree-ring width and stable isotopes (carbon, oxygen, and hydrogen) in tree-ring cellulose are widely used to reconstruct environmental conditions. The application of models capable to describe a variation of stable isotopes in annual tree rings can be a powerful tool for interpretation of environmental changes at the eco-physiological level. In this paper, we modelled carbon (δ13С), oxygen (δ18O), and hydrogen (δ2H) variations at the tree-ring level and compared results with measured data, obtained from the Mackenzie Delta River (68°30′ N, 133°48′ W) for the common period from 1901 to 2009. Using a process-based model (LPX), we were able to simulate carbon isotope values, which significantly (r = 0.29; p = 0.002) correlate with measured carbon isotope values. The model calculations for oxygen and hydrogen require further modifications and improvements, in particular the inclusion of the source of water used by the trees in the Canadian subarctic, as well as δ18O and δ2H in the water.

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Держатели документа:
Сибирский Федеральный Университет, 660041, пр. Свободный, 79, Красноярск, Российская Федерация
Институт физики им. Л.В. Киренского СО РАН, Академгородок, 50, г. Красноярск, Российская Федерация, 660036
Сибирский государственный университет науки и технологий имени академика М.Ф. Решетнева, Красноярск, Красноярский рабочий 31, 660037, Российская Федерация

Доп.точки доступа:
Васильева, Наталья Дмитриевна; Vasilieva, N. D.; Софронова, Светлана Николаевна; Sofronova, S. N.; Баринов, В. В.; Тайник, А. В.; Трушкина, Т. В.; Чуракова, О. В.; РусДендро-2023, Международная дендрохронологическая конференция(5 ; сентябрь 2023г. ; Воронеж)

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3.


    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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4.


    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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5.


    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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6.


   
    Wüstite stability in the presence of a CO2-fluid and a carbonate-silicate melt: Implications for the graphite/diamond formation and generation of Fe-rich mantle metasomatic agents / Y. V. Bataleva [et al.] // Lithos. - 2016. - Vol. 244. - P. 20-29, DOI 10.1016/j.lithos.2015.12.001. - Cited References: 68. - This work was supported by the Russian Science Foundation under grant no. 14-27-00054. The authors thank A. Moskalev for his assistance in the work preparation, A. Khokhryakov for useful suggestions throughout the study, and S. Ovchinnikov for his assistance in implementation of Mössbauer spectroscopy measurements. The authors thank editor M. Scambelluri, and two anonymous reviewers for their useful comments, which helped to profoundly improve the manuscript. . - ISSN 0024-4937
РУБ Geochemistry & Geophysics + Mineralogy
Рубрики:
EARTHS LOWER MANTLE
   FERRIC IRON CONTENT

   DIAMOND FORMATION

   MINERAL INCLUSIONS

   NATURAL DIAMOND

   OXIDATION-STATE

   DEEP MANTLECRUST

   LITHOSPHERIC MANTLE

   OXYGEN FUGACITY

   OCEANIC-CRUST

Кл.слова (ненормированные):
Wustite -- CO2-fluid -- Carbonate-silicate melt -- Decarbonation -- Graphite formation -- HPHT experiment
Аннотация: Experimental simulation of the interaction of wüstite with a CO2-rich fluid and a carbonate-silicate melt was performed using a multianvil high-pressure split-sphere apparatus in the FeO-MgO-CaO-SiO2-Al2O3-CO2 system at a pressure of 6.3GPa and temperatures in the range of 1150°C-1650°C and with run time of 20h. At relatively low temperatures, decarbonation reactions occur in the system to form iron-rich garnet (Alm75Prp17Grs8), magnesiowüstite (Mg#≤0.13), and CO2-rich fluid. Under these conditions, magnesiowüstite was found to be capable of partial reducing CO2 to C0 that leads to the formation of Fe3+-bearing magnesiowüstite, crystallization of magnetite and metastable graphite, and initial growth of diamond seeds. At T≥1450°C, an iron-rich carbonate-silicate melt (FeO~56wt.%, SiO2~12wt.%) forms in the system. Interaction between (Fe,Mg)O, SiO2, fluid and melt leads to oxidation of magnesiowüstite and crystallization of fayalite-magnetite spinel solid solution (1450°C) as well as to complete dissolution of magnesiowüstite in the carbonate-silicate melt (1550°C-1650°C). In the presence of both carbonate-silicate melt and CO2-rich fluid, dissolution (oxidation) of diamond and metastable graphite was found to occur. The study results demonstrate that under pressures of the lithospheric mantle in the presence of a CO2-rich fluid, wüstite/magnesiowüstite is stable only at relatively low temperatures when it is in the absolute excess relative to CO2-rich fluid. In this case, the redox reactions, which produce metastable graphite and diamond with concomitant partial oxidation of wüstite to magnetite, occur. Wüstite is unstable under high concentrations of a CO2-rich fluid as well as in the presence of a carbonate-silicate melt: it is either completely oxidized or dissolves in the melt or fluid phase, leading to the formation of Fe2+- and Fe3+-enriched carbonate-silicate melts, which are potential metasomatic agents in the lithospheric mantle. © 2015 Elsevier B.V.

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Держатели документа:
Sobolev Institute of Geology and Mineralogy, Siberian Branch of Russian Academy of Sciences, Koptyug ave 3, Novosibirsk, Russian Federation
Novosibirsk State University, Pirogova str 2, Novosibirsk, Russian Federation
Kirensky Institute of Physics, Siberian Branch of Russian Academy of Sciences, Akademgorodok 50, bld. 38, Krasnoyarsk, Russian Federation

Доп.точки доступа:
Bataleva, Yu. V.; Palyanov, Y .N.; Sokol, A. G.; Borzdov, Y. M.; Bayukov, O. A.; Баюков, Олег Артемьевич
}
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7.


   
    Toxicity and antioxidant activity of fullerenol C60,70 with low number of oxygen substituents / E. S. Kovel, A. G. Kicheeva, N. G. Vnukova [et al.] // Int. J. Mol. Sci. - 2021. - Vol. 22, Is. 12. - Ст. 6382, DOI 10.3390/ijms22126382. - Cited References: 93. - This research was funded by RFBR, N18-29-19003; RFBR, Krasnoyarsk Territory and Krasnoyarsk Regional Fund of Science, N20-44-243001; and partly supported by the Program of the Federal Service for Surveillance on Consumer Rights Protection and Human Wellbeing, Fundamental Study 2020-2025 (Russian Federation) . - ISSN 1661-6596
   Перевод заглавия: Токсичность и антиоксидантная активность фуллеренола C60,70 с низким количеством кислородных заместителей
Кл.слова (ненормированные):
fullerenol -- toxicity -- antioxidant activity -- reactive oxygen species -- bioluminescent assay -- hormesis
Аннотация: Fullerene is a nanosized carbon structure with potential drug delivery applications. We studied the bioeffects of a water-soluble fullerene derivative, fullerenol, with 10-12 oxygen groups (F10-12); its structure was characterized by IR and XPS spectroscopy. A bioluminescent enzyme system was used to study toxic and antioxidant effects of F10-12 at the enzymatic level. Antioxidant characteristics of F10-12 were revealed in model solutions of organic and inorganic oxidizers. Low-concentration activation of bioluminescence was validated statistically in oxidizer solutions. Toxic and antioxidant characteristics of F10-12 were compared to those of homologous fullerenols with a higher number of oxygen groups:F24-28 and F40-42. No simple dependency was found between the toxic/antioxidant characteristics and the number of oxygen groups on the fullerene’s carbon cage. Lower toxicity and higher antioxidant activity of F24-28 were identified and presumptively attributed to its higher solubility. An active role of reactive oxygen species (ROS) in the bioeffects of F10-12 was demonstrated. Correlations between toxic/antioxidant characteristics of F10-12 and ROS content were evaluated. Toxic and antioxidant effects were related to the decrease in ROS content in the enzyme solutions. Our results reveal a complexity of ROS effects in the enzymatic assay system.

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Держатели документа:
Institute of Biophysics SB RAS, FRC KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Institute of Physics SB RAS, FRC KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
FRC KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Institute of Fundamental Biology and Biotechnology, Siberian Federal University, Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Kovel, E. S.; Kicheeva, A. G.; Vnukova, N. G.; Внукова, Наталья Григорьевна; Churilov, G. N.; Чурилов, Григорий Николаевич; Stepin, E. A.; Kudryasheva, N. S.
}
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8.


   
    The role of rocks saturated with metallic iron in the formation of ferric carbonate-silicate melts: experimental modeling under PT-conditions of lithospheric mantle / Y. V. Bataleva [et al.] // Russ. Geol. Geophys. - 2015. - Vol. 56, Is. 1-2. - P. 143-154, DOI 10.1016/j.rgg.2015.01.008. - Cited References:68. - This work was supported by Integration project 31 from the Siberian Branch of the Russian Academy of Sciences and by grant 12-05-00740 from the Russian Foundation for Basic Research. . - ISSN 1068. - ISSN 1878-030X. -
РУБ Geosciences, Multidisciplinary
Рубрики:
OXYGEN FUGACITY
   DIAMOND FORMATION

   OXIDATION-STATE

   EARTHS MANTLE

Кл.слова (ненормированные):
carbonate-silicate melt -- graphite -- CO2 fluid -- iron carbide -- garnet -- redox gradient -- high-pressure experiment
Аннотация: Experimental modeling of the processes of formation of ferric carbonate-silicate melts through the carbonate-oxide-metal interaction is performed in the (Mg,Ca)CO3-SiO2-Al2O3-Fe0 system at 6.3 and 7.5 GPa and within 1150-1650 °C, using a multianvil high-pressure apparatus of “split-sphere” type (BARS). Two parallel reactions run in the subsolidus region (1150-1450 °C): decarbonation, producing pyrope-almandine (Fe# = 0.40-0.75) and CO2 fluid, and redox interaction between carbonate and Fe0, resulting in the crystallization of iron carbide in assemblage with magnesiowustite (Fe# = 0.75-0.85). It is shown that the reduction of carbonate or CO2 fluid by iron carbide and parallel redox interaction of magnesiowustite with CO2 produce graphite in assemblage with Fe3 + -containing magnesiowustite. In the temperature range of 1450-1650 °C, generation of carbonate-silicate melts coexisting with pyrope-almandine, magnesiowustite, magnetite, ferrospinel, and graphite takes place. The composition of the produced melts is as follows: SiO2 - 10-15 wt.%, X(FeO + Fe2O3) = 36-43 wt.%, and Fe3+/XFe - 0.18-0.23. These Fe3 + -enriched carbonate-silicate melts/fluids are saturated with carbon and are the medium of graphite crystallization. Oxide and silicate phases (almandine, ferrospinel, and magnetite) coexisting with graphite are also characterized by high Fe3+/XFe values. It has been established that Fe3 + -enriched carbonate-silicate melts can result from the interaction of Fe0-containing rocks with carbonated rocks. In the reduced mantle (with the presence of iron carbides or oxides), melts of this composition can be the source of carbon and the medium of graphite crystallization at once. After separation and ascent, these ferric carbonate-silicate melts can favor oxidizing metasomatism in the lithospheric mantle.

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Публикация на русском языке Роль пород, содержащих самородное железо, в образовании железистых карбонатно-силикатных расплавов: экспериментальное моделирование при P-T-параметрах литосферной мантии [Текст] / Ю. В. Баталева [и др.] // Геол. и геофиз. - Новосибирск : Изд-во СО РАН, 2015. - Т. 56 № 1-2. - С. 188-203

Держатели документа:
Russian Acad Sci, Siberian Branch, VS Sobolev Inst Geol & Mineral, Novosibirsk 630090, Russia.
Russian Acad Sci, Kirensky Inst Phys, Siberian Branch, Krasnoyarsk 660036, Russia.
Novosibirsk State Univ, Novosibirsk 630090, Russia.

Доп.точки доступа:
Bataleva, Yu. V.; Palyanov, Yu. N.; Sokol, A. G.; Borzdov, Yu. M.; Bayukov, O. A.; Баюков, Олег Артемьевич; Siberian Branch of the Russian Academy of Sciences [31]; Russian Foundation for Basic Research [12-05-00740]
}
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9.


   
    The role of oxygen in the formation of a continual metal shell strongly bonded to the carbon surface / G. N. Churilov, G. A. Glushenko, Ye. V. Tomashevich [et al.] // International conference "Functional materials" : book of abstracts / ed. V. N. Berzhansky ; org. com. S. G. Ovchinnikov [et al.]. - Simferopol, 2021. - P. 244-245. - Библиогр.: 3

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Доп.точки доступа:
Berzhansky, V. N. \ed.\; Бержанский, Владимир Наумович; Ovchinnikov, S. G. \org. com.\; Овчинников, Сергей Геннадьевич; Churilov, G. N.; Чурилов, Григорий Николаевич; Glushenko, G. A.; Глущенко, Гарий Анатольевич; Tomashevich, Ye. V.; Томашевич Е. В.; Nikolaev, N. S.; Николаев, Никита Сергеевич; Vnukova, N. G.; Внукова, Наталья Григорьевна; "Functional materials", International conference(2021 ; Oct. 4-8 ; Alushta, Russia); Крымский федеральный университет имени В.И. Вернадского
}
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10.


   
    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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11.


   
    The investigation of the influence of oxygen concentration in the gas mixture on nanodispersed oxides synthesis / I. V. Karpov [et al.] // IOP Conf. Ser.: Mater. Sci. Eng. - 2017. - Vol. 255, Is. 1. - Ст. 012008, DOI 10.1088/1757-899X/255/1/012008. - Cited References: 25
   Перевод заглавия: Исследование влияния концентрации кислорода в газовой смеси на синтез нанодисперсных оксидов
Кл.слова (ненормированные):
Cathodes -- Electrodes -- Particle size -- Vacuum applications -- Average particle size -- Cathode process -- Discharge gaps -- Energy of ions -- Influence of oxygen -- Low pressure arc -- Oxides synthesis -- Superheated gas -- Gases
Аннотация: Thermal effects in cathode space of low-pressure arc discharge, which contribute to the synthesis of nanopowders with an average particle size of less than 10 nm, are considered. One of the most important parameters, characterizing the cathode processes of vacuum arc, is a voltage drop across the discharge gap. All the gases demonstrate a decrease of a voltage drop across the discharge gap under the condition ofincreasing the gas pressure in the range of p = 10-3 - 1 Pa. Dissipation of energy of ions and electrons on gas molecules causes abrupt heating of the gas. Heat, coming from gas plasma, has a significant impact on evaporating material of a cathode. It can be assumed that a microdrop fraction, formed as a result of a cathode spraying in a liquid phase, will further evaporate in a superheated gas.

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Доп.точки доступа:
Karpov, I. V.; Ushakov, A. V.; Lepeshev, A. A.; Лепешев, Анатолий Александрович; Fedorov, L. Y.; Dorozhkina, E. A.; Karpova, O. N.; Shaikhadinov, A. A.; Demin, V. G.; Bachurina, E. P.; Lichargin, D. V.; Abkaryan, A. K.; Zeer, G. M.; Зеер Г.М.; Zharkov, S. M.; Жарков, Сергей Михайлович; International Scientific Conference Reshetnev Readings(20 ; 2016 ; Nov. 9-12 ; Krasnoyarsk)
}
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12.


   
    The influence of oxygen concentration on the formation of CuO and Cu2O crystalline phases during the synthesis in the plasma of low pressure arc discharge / A. V. Uschakov [et al.] // Vacuum. - 2016. - Vol. 128. - P. 123-127, DOI 10.1016/j.vacuum.2016.03.025. - Cited References: 19. - This study was supported by the Russian Foundation for Basic Research. (Project No 15-08-02132). . - ISSN 0042-207X
   Перевод заглавия: Влияние концентрации кислорода на формирование кристаллических фаз CuO и Cu2O в процессе синтеза в плазме дугового разряда низкого давления
РУБ Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
Nanoparticles
   Oxide

Кл.слова (ненормированные):
Oxides -- Vapor deposition -- X-ray diffraction -- Transmission electron microscopy (TEM) -- Catalytic properties
Аннотация: This paper describes the synthesis of copper oxide nanoparticles with different percentages of CuO and Cu2O phases. It was achieved by the control of the percentage of oxygen in the gas mixture (N2 + O2) in a plasma-chemical process of evaporation-condensation by means of low-pressure arc discharge. In all the experiments, the pressure in the plasma-chemical reactor remained constant at 60 Pa. By means of X-ray diffraction (XRD), high resolution transmission electron microscopy (HRTEM), energy-dispersive X-ray spectroscopy (EDS), Fourier transform infrared spectroscopy (FTIR) it was found that the average particle size was 6 nm, and Cu2O phase content decreases with increasing oxygen content in the gas mixture. High photocatalytic properties of Cu2O powder were shown by the example of the reaction of the methyl orange dye decomposition in water solution. The problems, associated with the performance of this method and the formation of crystalline phases, are discussed.

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Держатели документа:
Siberian Federal University, Russian Federation
Reshetnev Siberian State Aerospace University, Krasnoyarsk, Russian Federation
Krasnoyarsk Scientific Center of the Siberian Branch of the Russian Academy of Science, Krasnoyarsk, Russian Federation
Kirensky Institute of Physics, Russian Academy of Sciences, Russian Federation

Доп.точки доступа:
Uschakov, A. V.; Karpov, I. V.; Lepeshev, A. A.; Zharkov, S. M.; Жарков, Сергей Михайлович
}
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13.


   
    The FeIV-O• oxyl unit as a key intermediate in water oxidation on the FeIII-hydroxide: DFT predictions / A. A. Shubin, V. Y. Kovalskii, S. P. Ruzankin [et al.] // Int. J. Quantum Chem. - 2021. - Vol. 121, Is. 10. - Ст. e26610, DOI 10.1002/qua.26610. - Cited References: 21. - Aleksandr A. Shubin, Igor L. Zilberberg, and Valentin N. Parmon acknowledge the support of Russian Foundation for Basic Research under grant No. 15-29-01275. Viktor Yu. Kovalskii acknowledges the support of Russian Foundation for Basic Research under grant No. 18-33-00932. Calculations have been performed at the Siberian Supercomputer Centre SB RAS . - ISSN 0020-7608
Кл.слова (ненормированные):
negative spin density -- oxyl oxygen -- the FeOOH hydroxide -- the O-O coupling -- water oxidation
Аннотация: The O-O coupling process in water oxidation on the gamma FeOOH hydroxide catalyst is simulated by means of density functional theory using model iron cubane cluster Fe4O4(OH)4. A key reactive intermediate is proposed to be the HO-FeIV-O• oxyl unit with terminal oxo radical. The “initial” vertex FeIII(OH) moiety forms this intermediate at the calculated overpotential of 0.93 V by adding one water molecule and withdrawing two proton–electron pairs. The O-O coupling goes via water nucleophilic attack on the oxyl oxygen to form the O-O bond with a remarkably low barrier of 11 kcal/mol. This process is far more effective than alternative scenario based on direct interaction of two ferryl FeIV-O sites (with estimated barrier of 36 kcal/mol) and is comparable with the coupling between terminal oxo center and three-coordinated lattice oxo center (12 kcal/mol barrier). The process of hydroxylation of terminal oxygen inhibits the O-O coupling. Nevertheless, being more effective for ferryl oxygen, the hydroxylation in fact enhances selectivity of the O-O coupling initiated by the oxyl oxygen.

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Держатели документа:
Boreskov Institute of Catalysis, Novosibirsk, Russian Federation
Novosibirsk State University, Novosibirsk, Russian Federation
Kirensky Institute of Physics SB RAS, FRC “Krasnoyarsk Science Center SB RAS”, Krasnoyarsk, Russian Federation
National Research Tomsk State University, Tomsk, Russian Federation
Department of Chemistry, Kyungpook National University, Daegu, South Korea

Доп.точки доступа:
Shubin, A. A.; Kovalskii, V. Y.; Ruzankin, S. P.; Zilberberg, I. L.; Parmon, V. N.; Tomilin, F. N.; Томилин, Феликс Николаевич; Avramov, P. V.
}
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14.


   
    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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15.


   
    Synthesis, mass spectroscopy detection, and density functional theory investigations of the Gd endohedral complexes of C82 fullerenols / A. A. Shakirova, F. N. Tomilin, V. A. Pomogaev [et al.] // Computation. - 2021. - Vol. 9, Is. 5. - Ст. 58, DOI 10.3390/computation9050058. - Cited References: 41. - The experimental results were funded by RFBR project No. 18-29-19003 MK. The quantum chemical study was funded by project 0721-2020-0033 of the Russian Ministry of Science and Education. The collaboration and coordination of Russian and Korean teams was supported by Collaborative NRF-RFBR grant (Korean ID: NRF-2019K2A9A1A06100125; Russian ID: Project No. 19-53-51005 NIFa RFFI-Korea) and NRF 2021R1A2C1010455 grant . - ISSN 2079-3197
   Перевод заглавия: Синтез, масс-спектроскопическое определение и исследование теорией функционала плотности Gd-эндоэдральных комплексов фуллеренолов C82
РУБ Mathematics, Interdisciplinary Applications
Рубрики:
ZETA VALENCE QUALITY
   BIOLOGICAL-ACTIVITY

   BASIS-SETS

   TOXICITY

Кл.слова (ненормированные):
endohedral fullerenes -- density functional theory -- antioxidant activity -- reactive oxygen species -- magnetic resonance imaging
Аннотация: Gd endohedral complexes of C82 fullerenols were synthesized and mass spectrometry analysis of their composition was carried out. It was established that the synthesis yields a series of fullerenols Gd@C82Ox(OH)y (x = 0, 3; y = 8, 16, 24, 36, 44). The atomic and electronic structure and properties of the synthesized fullerenols were investigated using the density functional theory calculations. It was shown that the presence of endohedral gadolinium increases the reactivity of fullerenols. It is proposed that the high-spin endohedral fullerenols are promising candidates for application in magnetic resonance imaging.

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Держатели документа:
Siberian Fed Univ, Dept Biophys, Sch Engn Phys & Radio Elect, Sch Petr & Gas Engn, Pr Svobodny 79, Krasnoyarsk 660041, Russia.
Russian Acad Sci, Siberian Branch, Kirensky Inst Phys, Krasnoyarsk Sci Ctr, Akad Gorodok 50, Krasnoyarsk 660036, Russia.
Natl Res Tomsk State Univ, Dept Phys, Lenina Ave 36, Toms 634050, Russia.
Kyungpook Natl Univ, Dept Chem, 80 Daehak Ro, Daegu 41566, South Korea.
Kyungpook Natl Univ, Green Nano Mat Res Ctr, 80 Daehak Ro, Daegu 41566, South Korea.
Russian Acad Sci, Siberian Branch, Inst Biophys, Krasnoyarsk Sci Ctr, Akad Gorodok 50-50, Krasnoyarsk 660036, Russia.

Доп.точки доступа:
Shakirova, A. A.; Tomilin, F. N.; Томилин, Феликс Николаевич; Pomogaev, V. A.; Vnukova, N. G.; Внукова, Наталья Григорьевна; Churilov, G. N.; Чурилов, Григорий Николаевич; Kudryasheva, N. S.; Tchaikovskaya, O. N.; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич; Avramov, P. V.; RFBRRussian Foundation for Basic Research (RFBR) [18-29-19003 MK]; Russian Ministry of Science and EducationMinistry of Education and Science, Russian Federation [0721-2020-0033]; Collaborative NRF-RFBR grant (Korean) [NRF-2019K2A9A1A06100125]; Collaborative NRF-RFBR grant (Russian) [19-53-51005 NIFa RFFI-Korea]; NRF [2021R1A2C1010455]
}
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16.


   
    Synthesis of samarium oxysulfate Sm2O2SO4 in the high-temperature oxidation reaction and its structural, thermal and luminescent properties / Y. G. Denisenko, E. I. Sal'nikova, S. A. Basova [et al.] // Molecules. - 2020. - Vol. 25, Is. 6. - Ст. 1330, DOI 10.3390/molecules25061330. - Cited References: 56. - This research was funded by the Russian Foundation for Basic Research (Grants 18-02-00754, 18-32-20011) and Russian Science Foundation (project 19-42-02003). . - ISSN 1420-3049
   Перевод заглавия: Синтез оксисульфата самария Sm2O2SO4 в реакции высокотемпературного окисления и его структурные, термические и люминесцентные свойства
РУБ Biochemistry & Molecular Biology + Chemistry, Multidisciplinary
Рубрики:
RARE-EARTH SULFATES
   SPECTROSCOPIC PROPERTIES

   OXYGEN-STORAGE

   LN

   LA

Кл.слова (ненормированные):
samarium -- oxysulfate -- structure -- luminescence -- thermochemistry
Аннотация: The oxidation process of samariumoxysulfide was studied in the temperature range of 500–1000 °C. Our DTA investigation allowed for establishing the main thermodynamic (∆Hºexp = −654.6 kJ/mol) and kinetic characteristics of the process (Ea = 244 kJ/mol, A = 2 × 1010). The enthalpy value of samarium oxysulfate (ΔHºf (Sm2O2SO4(monocl)) = −2294.0 kJ/mol) formation was calculated. The calculated process enthalpy value coincides with the value determined in the experiment. It was established that samarium oxysulfate crystallizes in the monoclinic symmetry class and its crystal structure belongs to space group C2/c with unit cell parameters a = 13.7442 (2), b = 4.20178 (4) and c = 8.16711 (8)Å, β = 107.224 (1)°, V = 450.498 (9)Å3, Z = 4. The main elements of the crystalline structure are obtained and the cation coordination environment is analyzed in detail. Vibrational spectroscopy methods confirmed the structural model adequacy. The Sm2O2SO4 luminescence spectra exhibit three main bands easily assignable to the transitions from 4G5/2 state to 6H5/2, 6H7/2, and 6H9/2 multiplets.

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Держатели документа:
Ind Univ Tyumen, Dept Gen & Special Chem, Tyumen 625000, Russia.
Tyumen State Univ, Inst Chem, Tyumen 625003, Russia.
Northen Trans Ural Agr Univ, Dept Gen Chem, Tyumen 625003, Russia.
RAS, Fed Res Ctr, Kirensky Inst Phys, KSC,SB,Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Sch Engn Phys & Radioelect, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
RAS, Kirensky Inst Phys, Fed Res Ctr, KSC,SB,Lab Mol Spect, Krasnoyarsk 660036, Russia.
RAS, Kirensky Inst Phys, Fed Res Ctr, KSC,SB,Lab Coherent Opt, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Inst Nanotechnol Spect & Quantum Chem, Krasnoyarsk 660041, Russia.
Siberian Fed Univ, Sch Engn & Construct, Krasnoyarsk 660041, Russia.
RAS, Inst Semicond Phys, Lab Opt Mat & Struct, SB, Novosibirsk 630090, Russia.
Novosibirsk State Univ, Lab Semicond & Dielectr Mat, Novosibirsk 630090, Russia.
Kemerovo State Univ, Res & Dev Dept, Kemerovo 650000, Russia.
Tyumen State Univ, Res Resource Ctr, Nat Resource Management & Physicochem Res, Tyumen 625003, Russia.
RAS, Inst Solid State Chem, Lab Chem Rare Earth Cpds, UB, Ekaterinburg 620137, Russia.

Доп.точки доступа:
Denisenko, Yu. G.; Sal'nikova, E. I.; Basova, S. A.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Krylov, A. S.; Крылов, Александр Сергеевич; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Atuchin, V. V.; Volkova, S. S.; Khritokhin, N. A.; Andreev, O. V.; Russian Foundation for Basic ResearchRussian Foundation for Basic Research (RFBR) [18-02-00754, 18-32-20011]; Russian Science FoundationRussian Science Foundation (RSF) [19-42-02003]
}
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17.


   
    Structure of metastable Sr0.8Dy0.2Co3-δ phases and their electrical and magnetic properties / V. A. Dudnikov, S. N. Vereshchagin, L. A. Solov’ev [et al.] // J. Exp. Theor. Phys. - 2022. - Vol. 134, Is. 3. - P. 290-299, DOI 10.1134/S1063776122030037. - Cited References: 40. - Investigation was supported by the Russian Foundation for Basic Research (grant no. 19-03-00017). Thermal and X-ray diffraction studies were conducted in the framework of State Task 0287-2021-0013 for the Institute of Chemistry and Chemical Technologies, Siberian Branch, Russian Academy of Sciences . - ISSN 1063-7761
Кл.слова (ненормированные):
Cobalt alloys -- Metastable phases -- Oxygen -- Perovskite -- Temperature distribution
Аннотация: Polycrystalline Sr0.8Dy0.2Co3-δ complex cobalt oxides with a different amount of oxygen (δ = 0.26, 0.44, 0.46) have been prepared by solid-state synthesis. An increase in oxygen deficiency causes the brownmillerite phase to appear in the perovskite structure, which significantly changes its properties. At δ = 0.46, the content of the brownmillerite phase reaches 38%. A comparative analysis of the magnetic and transport properties of synthesized samples has been carried out. The asymptotic Curie temperature changes sign from positive at δ = 0.26 to negative at δ = 0.46. The magnetoresistance of the sample with δ = 0.46 is negative and exceeds 40% at T = 10 K. The temperature dependence of resistivity is characteristic of semiconductors, and the absolute values for samples at low temperatures differ almost tenfold.

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Публикация на русском языке Структура, электрические и магнитные свойства метастабильных фаз Sr0.8Dy0.2CoO3-δ [Текст] / В. А. Дудников, С. Н. Верещагин, Л. А. Соловьев [и др.] // Журн. эксперим. и теор. физ. - 2022. - Т. 161 Вып. 3. - С. 346-357

Держатели документа:
Kirenskii Institute of Physics, Siberian Branch, Russian Academy of Sciences, Krasnoyarsk, 660036, Russian Federation
Institute of Chemistry and Chemical Technologies, Siberian Branch, Russian Academy of Sciences, Krasnoyarsk, 660036, Russian Federation
Lebedev Physical Institute, Russian Academy of Sciences, Moscow, 119991, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Dudnikov, V. A.; Дудников, Вячеслав Анатольевич; Vereshchagin, S. N.; Solov’ev, L. A.; Gavrilkin, S. Y.; Tsvetkov, A. Y.; Sitnikov, M. V.; Ситников, Максим Владиславович; Orlov, Yu. S.; Орлов, Юрий Сергеевич
}
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18.


   
    Structural, magnetic, electronic, and dilatation properties of the ordered solid solutions Ln0.2Sr0.8CoO3-δ (Ln = Sm, Gd, Dy) with the same oxygen nonstoichiometry index δ / V. A. Dudnikov, Y. S. Orlov, M. V. Bushinsky [et al.] // J. Alloy. Compd. - 2020. - Vol. 830. - Ст. 154629, DOI 10.1016/j.jallcom.2020.154629. - Cited References: 44. - The work was financially supported by Russian Foundation for Basic Research (grant No. 19-03-00017); RFBR and BRFFR as a part of scientific project No. 18-52-00017 and project F18R-119; Russian Foundation for Basic Research, Government of Krasnoyarsk Territory, Krasnoyarsk Regional Fund of Science to the research project: "New thermoelectric materials based on multi-scale spatially inhomogeneous substituted rare-earth cobalt oxides and the Ruddlesden-Popper phases " project No. 18-42-243004, Project of Basic Research SB RAS V.45.3.3. . - ISSN 0925-8388. - ISSN 1873-4669
РУБ Chemistry, Physical + Materials Science, Multidisciplinary + Metallurgy & Metallurgical Engineering
Рубрики:
LN(1-X)SR(X)COO(3-DELTA) LN
   COBALTATE PEROVSKITES

Кл.слова (ненормированные):
Rare earth cobalt oxide solid solutions -- Layered perovskite-type cobalt oxides -- Structural -- Magnetic -- Electronic -- Dilatation properties
Аннотация: Single-phase samples of the layered perovskite-like cobalt oxides Ln0.2Sr0.8CoO3-δ (Ln = Sm, Gd, Dy) with the same oxygen nonstoichiometry index δ = 0.37 ± 0.01 were synthesized. All samples are characterized by a tetragonal unit cell with the space group I4/mmm. The structural, magnetic, electric transport and dilatation properties of the obtained samples are investigated. The studied samples are characterized by two anomalies in magnetic properties, a high-temperature maximum near Тm = 350 К with magnetic field hysteresis below Tm, and a diffuse peak in the intermediate temperature range, which shifts with ionic radius decrease of the rare-earth element to higher temperatures. The high-temperature maxima of the magnetic susceptibility correlate with anomalies in thermal expansion, heat capacity and the features in the temperature dependences of the electrical resistivity, pointing to a strong relationship between the structural, magnetic and electronic degrees of freedom. The given comparative analysis of the experimental data of various substituting rare-earth elements with the same oxygen nonstoichiometry has been carried out for the first time.

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Держатели документа:
RAS, Fed Res Ctr KSC SB, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.
RAS, Fed Res Ctr KSC SB, Inst Chem & Chem Technol, Krasnoyarsk 660036, Russia.
Lebedev Phys Inst, Moscow 119991, Russia.
NAS Belarus, Sci Pract Mat Res Ctr, Minsk 220072, BELARUS.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Russian Acad Sci, Ioffe Inst, St Petersburg 194021, Russia.

Доп.точки доступа:
Dudnikov, V. A.; Дудников, Вячеслав Анатольевич; Orlov, Yu. S.; Орлов, Юрий Сергеевич; Bushinsky, M. V.; Solovyov, L. A.; Vereshchagin, S. N.; Gavrilkin, S. Yu; Tsvetkov, A. Yu; Gorev, M. V.; Горев, Михаил Васильевич; Novikov, S. V.; Mantytskaya, O. S.; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич; Russian Foundation for Basic ResearchRussian Foundation for Basic Research (RFBR) [19-03-00017]; RFBRRussian Foundation for Basic Research (RFBR) [18-52-00017, F18R-119]; BRFFR [18-52-00017, F18R-119]; Russian Foundation for Basic Research, Government of Krasnoyarsk Territory [18-42-243004, SB RAS V.45.3.3]
}
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19.


   
    Structural, Magnetic, and Thermodynamic Properties of Ordered and Disordered Cobaltite Gd0.1Sr0.9CoO3 – δ / V. A. Dudnikov [et al.] // J. Exp. Theor. Phys. - 2019. - Vol. 128, Is. 4. - P. 630-640, DOI 10.1134/S1063776119020171. - Cited References: 27. - This work was supported by the Russian Foundation for Basic Research (grant nos. 17-02-00826, 16-02-00507, and 18-52-00017 Bel_a) and by the Council on Grants of the President of the Russian Federation (SP-1844.2016.1). X-ray spectra were recorded using the equipment of a unique scientific facility Kurchatov Synchrotron Radiation Source financed by the Ministry of Education and Science of the Russian Federation (project ID RFMEFI61917X0007). . - ISSN 1063-7761. - ISSN 1090-6509
Рубрики:
PROFILE REFINEMENT
   PHASE-TRANSITION

   OXYGEN SORPTION

   PEROVSKITE

Аннотация: The effect of cationic and anionic orderings on the crystal structure and magnetic properties of substituted rare-earth cobaltites Gd0.1Sr0.9CoO3 – δ was studied using X-ray diffraction, measurement of XANES spectra, and magnetic and thermodynamic characteristics. The effects of ordering cause a decrease in symmetry to tetragonal and a distortion of the coordination octahedra of CoO6. Anomalous magnetic and thermodynamic quantities are observed at 260 and 360 K, respectively, for disordered and ordered samples. The XANES spectra measured at the CoK edge did not reveal a noticeable shift in the absorption edge compared with the spectrum of original GdCoO3. This suggests that the charge compensation process is associated not only with a change in the electronic state of cobalt ions, but also with the emergence of holes in the 2p states of oxygen.

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Публикация на русском языке Структурные, магнитные и термодинамические свойства упорядоченного и разупорядоченного кобальтита Gd0.1Sr0.9CoO3-δ [Текст] / В. А. Дудников [и др.] // Журн. эксперим. и теор. физ. - 2019. - Т. 155 Вып. 4. - С. 737-749

Держатели документа:
Russian Acad Sci, Kirensky Inst Phys, Siberian Branch, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Russian Acad Sci, Inst Chem & Chem Technol, Siberian Branch, Krasnoyarsk 660036, Russia.
Russian Acad Sci, Lebedev Phys Inst, Moscow 119991, Russia.
Natl Res Ctr, Kurchatov Inst, Moscow 123182, Russia.
Natl Acad Sci Belarus, Sci & Pract Mat Res Ctr, Minsk 220072, BELARUS.

Доп.точки доступа:
Dudnikov, V. A.; Дудников, Вячеслав Анатольевич; Kazak, N. V.; Казак, Наталья Валерьевна; Orlov, Yu. S.; Орлов, Юрий Сергеевич; Vereshchagin, S. N.; Gavrilkin, S. Yu.; Tsvetkov, A. Yu.; Gorev, M. V.; Горев, Михаил Васильевич; Veligzhanin, A. A.; Trigub, A. L.; Troyanchuk, I. O.; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич; Russian Foundation for Basic Research [17-02-00826, 16-02-00507, 18-52-00017 Bel_a]; Russian Federation [SP-1844.2016.1]; Ministry of Education and Science of the Russian Federation [RFMEFI61917X0007]
}
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20.


   
    Strong spin triplet contribution of the first removal state in the insulating regime of Bi2Sr2Ca1-xYxCu2O8+delta / C. . Janowitz [et al.] // JETP Letters. - 2004. - Vol. 80, Is. 11. - P. 692-696, DOI 10.1134/1.1862796. - Cited References: 18 . - ISSN 0021-3640
РУБ Physics, Multidisciplinary
Рубрики:
ELECTRONIC-STRUCTURE
   APICAL OXYGEN

   MODEL

   SUPERCONDUCTIVITY

   ONSET

Аннотация: The experimental dispersion of the first removal state in the insulating Bi2Sr2Ca1 - xYxCu2O8 + delta regime is found to differ significantly from that of other parent materials: oxyclorides and La2CuO4. For Y contents of 0.92 greater than or equal to x greater than or equal to 0.55 due to nonstoichiometric effects in the Bi-O layers, the hole concentration in the CuO2 layers is almost constant and, on the contrary, the crystal lattice parameters a, b, c change very strongly. This (a, b) parameter increase and c parameter decrease results in an unconventional three peak structure at (0, 0), (pi/2, pi/2), (pi, pi) for x = 0.92. We can describe the experimental data only beyond the framework of the three-band p-d-model involving the representations of a new triplet counterpart for the Zhang-Rice singlet state. (C) 2004 MAIK "Nauka/Interperiodica".

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Держатели документа:
Humboldt Univ, Inst Phys, D-12489 Berlin, Germany
Russian Acad Sci, LV Kirensky Phys Inst, Krasnoyarsk 660036, Russia
ИФ СО РАН
Institute of Physics, Humboldt University of Berlin, 12489 Berlin, Germany
Kirensky Institute of Physics, Russian Academy of Sciences, Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Janowitz, C.; Seidel, U.; Unger, RST; Krapf, A.; Manzke, R.; Gavrichkov, V. A.; Гавричков, Владимир Александрович; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич
}
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