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1.


    Паршин, Александр Михайлович.
    Конфигурации директора в структурах нематика, адсорбированного на поверхности полимера / А. М. Паршин, В. Я. Зырянов, В. Ф. Шабанов // Жидк. кристаллы и их практич. использ. - 2015. - Т. 15, Вып. 1. - С. 56-65 ; Liquid Crystals and their Application. - Библиогр.: 20. - Работа выполнена частично при финансовой поддержке программ Президиума РАН и РФФИ (грант № 15-02-06924). . - ISSN 1991-3966
   Перевод заглавия: Director configurations in the structures of the nematic adsorbed on a polymer surface
Кл.слова (ненормированные):
нематический жидкий кристалл -- полимер -- адсорбция -- дисклинация -- конфигурация директора -- nematic liquid crystal -- polymer -- adsorption -- disclination -- director configuration
Аннотация: Исследованы ориентационные структуры нематических жидких кристаллов, возникающие на поверхности полимера в результате адсорбции, и их устойчивость относительно шлирен-текстуры. Изучены особенности точечных и линейных сингулярностей в исследуемых структурах. Рассмотрены конфигурации директора в слое нематика, определяемые комбинацией двух ориентирующих факторов: воздействием линейной дисклинации, фактора, стремящегося задать однородное планарное упорядочение, а также влиянием точечного дефекта, задающего радиальную структуру директора. С использованием расчетного метода проведен сравнительный анализ энергии упругих искажений поля директора для различных видов конфигураций: радиально-планарной, радиально-гомеотропной и радиально-радиальной в зависимости от толщины слоя нематика.
The orientational structures of nematic liquid crystals that form at the polymer surface due to adsorption and their stability with respect to the schlieren texture are investigated. Features of point and linear singularities in these structures are studied. The director configurations in nematic layer as a result of the combination of two aligning factors, which are the linear disclination that tends to impose uniform planar ordering and point defect that imparts the radial structure to the director are considered. The analysis of the elastic distortions energies of the director configurations for the radial-planar, radial-homeotropic and radial-radial structures, depending on the nematic layer thickness was performed using the calculation method.

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Держатели документа:
Институт физики им. Л.В. Киренского СО РАН

Доп.точки доступа:
Зырянов, Виктор Яковлевич; Zyryanov, V. Ya.; Шабанов, Василий Филиппович; Shabanov, V. F.; Parshin, A. M.

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2.


   
    Влияние ионного сурфактанта на энергию сцепления жидкого кристалла с поверхностью, исследованное с использованием магнитных пороговых полей перехода Фредерикса / А. М. Паршин [и др.] // Жидк. кристаллы и их практич. использ. - 2018. - Т. 18, № 3. - С. 59-66 ; Liq. Cryst. Appl., DOI 10.18083/LCAppl.2018.3.59. - Библиогр.: 25. - В. С. Сутормин благодарен РФФИ за поддержку исследований по гранту № 16-32-60036 мол_а_дк. . - ISSN 1991-3966. - ISSN 2499-9644
   Перевод заглавия: Influence of ionic surfactant on the anchoring energy of liquid crystal with a surface investigated using magnetic threshold fields of Freedericksz transition
РУБ Crystallography
Рубрики:
WALL INTERFACE
   TEMPERATURE-DEPENDENCE

   NEMATIC DROPLETS

   ADSORPTION

Кл.слова (ненормированные):
нематический жидкий кристалл -- ионный сурфактант -- энергия сцепления -- магнитное поле -- переход Фредерикса -- nematic liquid crystal -- ionic surfactant -- anchoring energy -- magnetic field -- Freedericksz transition
Аннотация: Исследовано сцепление нематического жидкого кристалла 5ЦБ и 5ЦБ, допированного ионным сурфактантом ЦТАБ, в ячейках с плоскопараллельными ограничивающими поверхностями. Получены зависимости интенсивности проходящего лазерного излучения от величины магнитного поля для ячеек с различными толщинами слоя нематика при различных температурах. Из пороговых полей перехода Фредерикса определены значения полярной энергии сцепления жидкого кристалла с поверхностью. Изучено влияние ионного сурфактанта на энергию сцепления, установлено, что добавление в объем жидкого кристалла ионного сурфактанта ведет к ее ослаблению. Проведен анализ точности определения энергии сцепления на основе выражения, следующего из соотношения Рапини – Популара. Показано, что лучшее экспериментальное разрешение энергии сцепления достигается при использовании тонких слоев нематика, более сильных магнитных полей, а также слабого сцепления молекул жидкого кристалла с поверхностью.
The coupling of nematic liquid crystal 5CB and 5CB doped with ionic surfactant CTAB in the cells with plane parallel interfaces was studied. For the cells with the varied nematic layer thickness at different temperatures, the dependencies of the passed laser radiation intensity on the magnetic field were obtained. From the threshold fields of Freedericksz transition, the polar anchoring energy of the liquid crystal to the surface was determined. The effect of the ionic surfactant on the anchoring energy was studied and it was found that the addition of the ionic surfactant to liquid crystal weakens the anchoring energy. The analysis of the accuracy of the anchoring energy determination based on the expression following from the Rapini - Popular relation was carried out. It was shown that the best experimental resolution of the anchoring energy is achieved when the thin nematic layers, stronger magnetic fields and weak anchoring of the liquid crystal molecules with the surface are used.

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Держатели документа:
Институт физики им. Л. В. Киренского, Федеральный исследовательский центр «Красноярский научный центр Сибирского отделения Российской академии наук», Академгородок, 50, 660036 Красноярск, Россия
Сибирский Федеральный университет, пр. Свободный, 79, 660041 Красноярск, Россия

Доп.точки доступа:
Паршин, Александр Михайлович; Parshin, A. M.; Сутормин, Виталий Сергеевич; Sutormin, V. S.; Зырянов, Виктор Яковлевич; Zyryanov, V. Ya.; Шабанов, Василий Филиппович; Shabanov, V. F.

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3.


   
    Theoretical investigation of the adsorption and diffusion of hydrogen on the surface and in the bulk of the intermetallic compound Mg2Ni / A. A. Kuzubov [et al.] // Phys. Solid State. - 2014. - Vol. 56, Is. 10. - P. 2035-2042, DOI 10.1134/S1063783414100187. - Cited References: 30 . - ISSN 1063-7834. - ISSN 1090-6460
РУБ Physics, Condensed Matter
Рубрики:
STORAGE MATERIAL Mg2NiH4
   INITIO MOLECULAR-DYNAMICS

   AUGMENTED-WAVE METHOD

   MINIMUM ENERGY PATHS

   ELASTIC BAND METHOD

   TEMPERATURE STRUCTURE

   SADDLE-POINTS

   ALLOYS

   TRANSITION

   MAGNESIUM

Аннотация: The intermetallic compound Mg2Ni as a potential material for hydrogen storage has been investigated theoretically. The sorption and diffusion of a hydrogen atom in the bulk and on the surface of this material, as well as the step-by-step process of dissociative chemisorption of a H-2 molecule on the surface, have been considered. The dependence of the sorption energy of atomic hydrogen on the structural characteristics of the intermetallic compound Mg2Ni has been analyzed.

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Публикация на русском языке Теоретическое изучение сорбции и диффузии водорода на поверхности и в объеме интерметаллида Mg2Ni [Текст] / А. А. Кузубов [и др.] // Физ. тверд. тела. - 2014. - T. 56 Вып. 10. - С. 1970-1977

Держатели документа:
Siberian Fed Univ, Krasnoyarsk 660041, Russia
Russian Acad Sci, Siberian Branch, Kirensky Inst Phys, Krasnoyarsk 660036, Russia
Siberian State Technol Univ, Krasnoyarsk 660049, Russia

Доп.точки доступа:
Kuzubov, A. A.; Кузубов, Александр Александрович; Eliseeva, N. S.; Krasnov, P. O.; Краснов, Павел Олегович; Kuklin, A. V.; Куклин, Артем Валентинович; Kovaleva, E. A.; Kholtobina, A. S.
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4.


   
    The effect of copper and iron adsorption on the catalytic performance of alumina nanofiber / nanodiamond composite in sensing applications / N. O. Ronzhin, E. D. Posokhina, E. V. Mikhlina [et al.] // J. Phys. Chem. Solids. - 2022. - Vol. 167. - Ст. 110785, DOI 10.1016/j.jpcs.2022.110785. - Cited References: 68. - This work is supported by the Russian Foundation for Basic Research, Project 18–29–19078. The authors would like to express their special thanks to Krasnoyarsk Regional Center of Research Equipment of Federal Research Center «Krasnoyarsk Science Center SB RAS» for providing the equipment to ensure the accomplishment of this project . - ISSN 0022-3697
Кл.слова (ненормированные):
Nanodiamonds -- Alumina nanofibers -- Indicator system -- Copper ions -- Iron ions -- Phenol detection
Аннотация: Phenolic compounds are common environmental pollutants, which are used in many industries and contaminate water environment due to industrial wastewater discharge. Presently, there is an increasing demand for the development and improvement of inexpensive, easy-to-use analytical tools for in-situ detection of phenolic compounds. In this work, we investigate the effect of adsorption of Cu2+ and Fe2+ ions on the catalytic activity of a composite material based on alumina nanofibers (ANF) and detonation nanodiamonds (DND) in the co-oxidation of phenols with 4-aminoantipyrine in the presence of hydrogen peroxide. We have found more than two-fold increase of the catalytic activity for ANF + DND + Cu composite, while the activity of ANF + DND + Fe composite is found to decrease by several times in comparison with the original ANF + DND material. The results of FTIR analysis indicate that the adsorption of iron ions occurs with the formation of hydroxide surface groups and hydrogen bonds, which apparently block their catalytic activity in the Fenton redox cycle. The higher catalytic performance of AND + DND composite functionalized with copper ions makes it possible to detect two times lower concentrations of analytes (phenol and 4-chlorophenol) in comparison with the original composite. It is shown that the AND + DND + Cu composite provides a linear yield of the co-oxidation reaction product in a wide range of analyte concentrations (0.25–100 μM for phenol and 0.5–25 μM for 4-chlorophenol). Model experiments demonstrate the applicability of copper-functionalized composite as a reusable sensor for the determination of phenol in aqueous samples.

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Держатели документа:
Institute of Biophysics SB RAS, Akademgorodok 50/50, Krasnoyarsk, 660036, Russian Federation
Institute of Computational Modelling SB RAS, Akademgorodok 50/44, Krasnoyarsk, 660036, Russian Federation
Kirensky Institute of Physics SB RAS, Akademgorodok 50/38, Krasnoyarsk, 660036, Russian Federation
Federal Research Center KSC SB RAS, Akademgorodok 50/38, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Svobodny 79, Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Ronzhin, N. O.; Posokhina, E. D.; Mikhlina, E. V.; Shestakov, N. P.; Шестаков, Николай Петрович; Nemtsev, I. V.; Немцев, Иван Васильевич; Bondar, V. S.; Ryzhkov, I. I.
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5.


   
    Template synthesis of CMK-3 nanostructured carbon material and study of its properties / I. V. Ponomarenko [et al.] // Glass Phys. Chem. - 2014. - Vol. 40, Is. 1. - P. 79-87, DOI 10.1134/S1087659614010180 . - ISSN 1087-6596
Кл.слова (ненормированные):
adsorption of N2 -- CMK-3 mesostructured carbon -- mesoporous mesostructured silicates -- SBA-15 -- template synthesis -- transmission electron microscopy -- X-ray diffraction
Аннотация: Mesostructured carbon has been obtained by template synthesis. SBA-15 mesostructured silicate has been used as a template. The effect of the properties of a template on the ordering of a replica has been studied. It has been shown with the use of X-ray diffraction, gas adsorption, and electron microscopy that there are evident correlations of the conditions of synthesis of a template with the ordering of a carbon replica, which can be guided by the synthesis of materials. The ordering of a replica significantly depends on the mesopore volume of the initial template and thickness of the pore wall. One should use templates with the highest possible mesopore volume and minimal wall thickness to obtain highly ordered replicas. These templates can be prepared during the treatment of synthesized materials at temperatures close to 100 C. It has been determined that, when there is SBA-15, the presence of micropores is a necessary condition for the preparation of carbon replicas that retain the structure of the template. © 2014 Pleiades Publishing, Ltd.

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Держатели документа:
Institute of Chemistry and Chemical Engineering, Russian Academy of Sciences, Siberian Branch, Akademgorodok 50/24, Krasnoyarsk 660036, Russian Federation
Siberian Federal University, pr. Svobodnyi 79, Krasnoyarsk 660049, Russian Federation

Доп.точки доступа:
Ponomarenko, I. V.; Parfenov, V. A.; Zaitseva, Y. N.; Zharkov, S. M.; Жарков, Сергей Михайлович; Kirik, S. D.
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6.


   
    Temperature dependent elastic repulsion of colloidal nanoparticles with a polymer adsorption layer / A. P. Gavrilyuk [et al.] // Colloid Polym. Sci. - 2018. - Vol. 296, Is. 10. - P. 1689-1697, DOI 10.1007/s00396-018-4383-y. - Cited References: 49. - The reported research was funded by the Russian Foundation for Basic Research, the government of the Krasnoyarsk territory and Krasnoyarsk Regional Fund of Science, grant 18-42-243023, the RF Ministry of Science and Education, the State contract with Siberian Federal University for scientific research in 2017-2019, and SB RAS Program No II.2P (0358-2015-0010). . - ISSN 0303-402X. - ISSN 1435-1536
РУБ Chemistry, Physical + Polymer Science
Рубрики:
STERICALLY-STABILIZED PARTICLES
   DEPLETION FLOCCULATION

   AGGREGATION

Кл.слова (ненормированные):
Nanoparticle -- Adsorption layer -- Elastic deformation -- Coagulation -- kinetics -- Elasticity modulus
Аннотация: The model of pairwise elastic repulsion of contacting colloidal nanoparticles with a rigid core and deformable shell is discussed. A simple analytical equation is applied for the energy of elastic repulsion of nanoparticles with arbitrary sizes and the elasticity moduli of self-healing polymer adsorption layers. The model is based on the representation of the absorption layer as a continuous medium that is elastically deformed upon the contact of nanoparticles. The major characteristic of this medium is the elasticity modulus. The magnitude of the elasticity modulus is determined from the condition of balance of the van der Waals attractive forces of nanoparticles and the elastic repulsion of their adsorption layers in the contact area, taking into account the temperature variations. We employed the kinetic approach to describe the dependence of the elasticity modulus on both the temperature and the rate of its change.

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Держатели документа:
RAS, SB, Inst Computat Modeling, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Inst Math & Comp Sci, Krasnoyarsk 660041, Russia.
Siberian Fed Univ, Lab Nanotechnol Spect & Quantum Chem, Krasnoyarsk 660041, Russia.
RAS, SB, Fed Res Ctr KSC, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.
Siberian State Univ Sci & Technol, Krasnoyarsk 660014, Russia.

Доп.точки доступа:
Gavrilyuk, A. P.; Gerasimov, V. S.; Герасимов, Валерий Сергеевич; Ershov, A. E.; Ершов, Александр Евгеньевич; Karpov, S. V.; Карпов, Сергей Васильевич; Russian Foundation for Basic Research; government of the Krasnoyarsk territory and Krasnoyarsk Regional Fund of Science [18-42-243023]; RF Ministry of Science and Education,; State contract with Siberian Federal University for scientific research in 2017-2019; SB RAS Program [II.2P (0358-2015-0010)]
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7.


   
    Tailoring adsorption induced switchability of a pillared layer MOF by crystal size engineering / L. Abylgazina, I. Senkovska, S. Ehrling [et al.] // CrystEngComm. - 2021. - Vol. 23, Is. 3. - P. 538-549, DOI 10.1039/d0ce01497d. - Cited References: 71. - The authors thank the DFG (FOR 2433 MOF Switches, Project No. 279409724) for financial support. P.P. and J. D. E. thank Center for Information Services and High Performance Computing (ZIH) at TU Dresden for providing high-performance computing facilities. Authors acknowledge Helmholtz-Zentrum Berlin für Materialien und Energie for allocated beamtime at KMC-2 and MX14.2 beamlines. J. D. E. acknowledges the support of the Alexander von Humboldt foundation and HPC platforms provided by a GENCI grant (A0070807069) . - ISSN 1466-8033
Кл.слова (ненормированные):
Adsorption -- Crystals -- Dichloromethane -- Hinges -- Nickel metallography -- Particle size -- Zinc metallography
Аннотация: The pillared layer framework DUT-8(Zn) (Zn2(2,6-ndc)2(dabco), 2,6-ndc = 2,6-naphthalenedicarboxylate, dabco = 1,4-diazabicyclo-[2.2.2]-octane, DUT = Dresden University of Technology) is a prototypical switchable MOF, showing characteristic adsorption and desorption induced open phase (op) to closed phase (cp) transformation associated with huge changes in cell volume. We demonstrate switchability strongly depends on a framework-specific critical particle size (dcrit). Superposed, the solvent removal process (pore desolvation stress contracting the framework) significantly controls the cp/op ratio after desolvation and, subsequently, the adsorption induced switchability characteristics of the system. After desolvation, the dense cp phase of DUT-8(Zn) shows no adsorption-induced reopening and therefore is non-porous for N2 at 77 K and CO2 at 195 K. However, polar molecules with a higher adsorption enthalpy, such as chloromethane at 249 K and dichloromethane (DCM) at 298 K can reopen the macro-sized crystals upon adsorption. For macro-sized particles, the outer surface energy is negligible and only the type of metal (Zn, Co, Ni) controls the DCM-induced gate opening pressure. The node hinge stiffness increases from Zn to Ni as confirmed by DFT calculations, X-ray crystal structural analysis, and low frequency Raman spectroscopy. This softer Zn-based node hinges and overall increased stabilization of cp vs. op phase shift the critical particle size at which switchability starts to become suppressed to even lower values (dcrit ‹ 200 nm) as compared to the Ni-based system (dcrit ≈ 500 nm). Hence, the three factors affecting switchability (energetics of the empty host, (Eop–Ecp) (I), particle size (II), and desolvation stress (III)) appear to be of the same order of magnitude and should be considered collectively, not individually.

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Держатели документа:
Department of Inorganic Chemistry i, Technische Universitat Dresden, Bergstrasse 66, Dresden, 01069, Germany
Faculty of Chemistry and Pharmacy, University of Sofia, Sofia, 1126, Bulgaria
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Abylgazina, L.; Senkovska, I.; Ehrling, S.; Bon, V.; St. Petkov, P.; Evans, J. D.; Krylova, S. N.; Крылова, Светлана Николаевна; Krylov, A. S.; Крылов, Александр Сергеевич; Kaskel, S.
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8.


   
    Study of interaction between transition metal atoms and bigraphene monovacancy by means of quantum chemistry / A. A. Kuzubov [et al.] // Comput. Mater. Sci. - 2016. - Vol. 112, Part A. - P. 269-275, DOI 10.1016/j.commatsci.2015.11.002. - Cited References: 39. - The authors would like to thank Siberian Supercomputer Center (SSCC) of SB RAS, Novosibirsk; and L.V. Kirensky Institute of Physics of SB RAS, Krasnoyarsk, for providing the access to their supercomputers. This work was supported by the government contract of the Ministry of Education and Science of the Russian Federation to Siberian Federal University (Grant No. 16.1500.2014/K). . - ISSN 0927-0256
РУБ Materials Science, Multidisciplinary
Рубрики:
INITIO MOLECULAR-DYNAMICS
   MASSLESS DIRAC FERMIONS

   GRAPHENE

   VACANCIES

   POINTS

   GAS

Кл.слова (ненормированные):
Bigraphene -- Spintronics -- Transition metal -- Adsorption -- Migration
Аннотация: First-row transition metal atoms adsorption on bigraphene monovacancy was studied within the framework of DFT in periodic boundary conditions. Electronic and magnetic properties of composites were analyzed and their potential utilization in spintronics was discussed. Barriers of metal atoms migration from bigraphene surface to the interlayer space through the vacancy were estimated in order to consider both thermodynamic and kinetic aspects of composites experimental preparation. Formation of metal atoms inner-sorbed on bigraphene was found to demand harsh synthesis conditions; whereas outer-sorbed composites demonstrate significantly higher degree of spin polarization which makes them perspective for usage in spintronic devices. © 2015 Elsevier B.V.

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Держатели документа:
Siberian Federal University, 79 Svobodny pr., Krasnoyarsk, Russian Federation
L.V. Kirensky Institute of Physics, 50 Akademgorodok, Krasnoyarsk, Russian Federation
Kyungpook National University, 80 Daehakro, Bukgu, Daegu, South Korea

Доп.точки доступа:
Kuzubov, A. A.; Кузубов, Александр Александрович; Avramov, P. V.; Аврамов, Павел Вениаминович; Nikolaeva, K. M.; Mikhaleva, N. S.; Kovaleva, E. A.; Kuklin, A. V.; Куклин, Артем Валентинович; Fedorov, A. S.; Федоров, Александр Семенович
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9.


   
    Simultaneous ion exchange recovery of platinum and rhodium from chloride solutions / O. N. Kononova [et al.] // Hydrometallurgy. - 2011. - Vol. 105, Is. 3-4. - P. 341-349, DOI 10.1016/j.hydromet.2010.11.009. - Cited Reference Count: 46 . - JAN. - ISSN 0304-386X
Рубрики:
GROUP-METALS PGM
   SEPARATION

   CATALYST

   ANION

   ADSORPTION

   EXTRACTION

   CHEMISTRY

   RESIN

Кл.слова (ненормированные):
platinum -- rhodium -- sorption -- anion exchangers -- chloride solutions -- anion exchangers -- chloride solutions -- platinum -- rhodium -- sorption -- ammonium thiocyanate -- anion exchangers -- basic parameters -- chemical structure -- chloride solutions -- diffusion coefficients -- distribution coefficient -- exchange capacities -- kinetic properties -- noble metals -- purolite -- rhodium chloride -- separation factors -- sorption ability -- work focus -- ammonium compounds -- chlorine compounds -- desorption -- hydrochloric acid -- ion exchange -- ion exchange resins -- ions -- platinum -- platinum compounds -- potassium hydroxide -- precious metals -- recovery -- rhodium -- sulfuric acid -- thioureas -- urea -- rhodium compounds
Аннотация: This work focuses on the sorption recovery of platinum (II, IV) and rhodium (III) simultaneously present in chloride solutions, freshly prepared and stored over 3 months, on commercial anion exchangers with different physical and chemical structure. The sorption was carried out from solutions with 0.001-4.0 mol/L HCl. The initial platinum and rhodium concentrations in contacting solutions were 0.25-2.5 mmol/L Sorption and kinetic properties of the chosen anion exchangers were investigated and the basic parameters of exchange capacity, recovery, distribution coefficients, separation factors, process rate, diffusion coefficients and half-exchange times were calculated. It is shown that anion exchangers investigated possess high sorption ability to platinum and rhodium chloride complexes, which does not deteriorate in case of stored solutions. Desorption of platinum and rhodium from the resins investigated was carried out with hydrochloric acid (2 mol/L), thiourea (1 mol/L) in sulfuric acid (2 mol/L) or in potassium hydroxide (2 mol/L) as well as by ammonium thiocyanate (2 mol/L). It was shown that complete separation of platinum and rhodium can be carried out with 2 mol/L HCl on anion exchanger Purolite S 985, whereas 2 mol/L NH(4)SCN as an elution agent leads to complete separation of noble metals on anion exchangers Purolite S 985, Purolite A 500 and AM-2B. (C) 2010 Elsevier B.V. All rights reserved.

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Держатели документа:
Siberian Fed Univ, Dept Chem, Krasnoyarsk 660041, Russia
Russian Acad Sci, LV Kirensky Phys Inst, Siberian Dept, Krasnoyarsk 660036, Russia

Доп.точки доступа:
Kononova, O.N.; Melnikov, A.M.; Borisova, T.V.; Krylov, A. S.; Крылов, Александр Сергеевич
}
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10.


   
    Selective adsorption capacity of Fe3O4@C nanoparticles with respect to organic cationic dyes / O. S. Ivanova, I. S. Edelman, A. Е. Sokolov [et al.] // The Sixth Asian school-conference on physics and technology of nanostructured materials : Proceedings. - VLadivostok, 2022. - Ст. IV.p.14. - P. 231-232. - Cited References: 3 . - ISBN 987-5-8044-1716-2
Рубрики:

Аннотация: The Fe3O4 and core-shell Fe3O4@C magnetic nanoparticles (NPs) with an average size of 15 ± 2 nm were synthesized and characterized. Comparative study of two types of NPs revealed their different sorption capacity of cationic and anionic dyes. The leading role of electrostaticinteractions in the dyes adsorption by Fe3O4@C NPs has been revealed.

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Держатели документа:
Kirensky Institute of Physics, FRC KSC SB RAS
Department of Applied Physics, National Pingtung University

Доп.точки доступа:
Ivanova, O. S.; Иванова, Оксана Станиславовна; Edelman, I. S.; Эдельман, Ирина Самсоновна; Sokolov, A. Е.; Соколов, Алексей Эдуардович; Svetlitsky, E. S.; Светлицкий, Евгений Сергеевич; Lin, C.-R.; Chun-Rong Lin; Chen, Y. -Z.; Ying-Zhen Chen; Tseng, Y.-T.; Yaw-Teng Tseng; Asian School-Conference on Physics and Technology of Nanostructured Materials(6 ; 2022 ; Apr. 25-29 ; Vladivostok); Азиатская школа-конференция по физике и технологии наноструктурированных материалов(6 ; 2022 ; 25-29 апр. ; Владивосток)
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11.


   
    Preparation and characterization of colloidal copper xanthate nanoparticles / Y. Mikhlin [et al.] // New J. Chem. - 2016. - Vol. 40, Is. 4. - P. 3059-3065, DOI 10.1039/c6nj00098c. - Cited References:50. - This research was supported by the Russian Science Foundation grant 14-17-00280. We thank Dr Roberto Felix Duarte (HZB) and bilateral program "German-Russian laboratory at BESSY II" for assistance with the X-ray absorption experiments. . - ISSN 1144-0546. - ISSN 1369-9261
   Перевод заглавия: Получение и исследование коллоидных наночастиц ксантогената меди
РУБ Chemistry, Multidisciplinary
Рубрики:
X-ray-absorption
   Self-assembled monolayers

   Sulfide nanoparticles

   Electronic-structure

   Waste-water

   Complexes

   Flotation

   Spectroscopy

   Adsorption

   Oxidation

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

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

Доп.точки доступа:
Mikhlin, Y. L.; Михлин, Юрий Леонидович; Vorobyev, S.; Saikova, S. V.; Сайкова, С. В.; Tomashevich, Y.; Fetisova, O.; Kozlova, S.; Zharkov, S. M.; Жарков, Сергей Михайлович; Russian Science Foundation [14-17-00280]
}
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12.


   
    Potential energy surfaces of adsorption and migration of transition metal atoms on nanoporus materials: The case of nanoporus bigraphene and G-C3N4 / I. Melchakova, K. M. Nikolaeva, E. A. Kovaleva [et al.] // Appl. Surf. Sci. - 2021. - Vol. 540. - Ст. 148223, DOI 10.1016/j.apsusc.2020.148223. - Cited References: 39. - The authors would like to thank Joint Supercomputer Center of RAS, Moscow; Center of Equipment for Joint Use of Siberian Federal University, Krasnoyarsk; and Information Technology Centre, Novosibirsk State University for providing the access to their supercomputers. Publication was supported by Project FSWM-2020-0033 of Russian Ministry of Science and Education . - ISSN 0169-4332
   Перевод заглавия: Поверхностная потенциальная энергия адсорбции и миграции атомов переходных металлов на нанопористых материалах: случай нанопористого биграфена и G-C3N4
Кл.слова (ненормированные):
Bigraphene -- g-C3N4 -- Transition metal -- Adsorption -- Migration
Аннотация: First-row transition metal (TM) atoms adsorption and migration on nanoporus 2D materials like bigraphene with double vacancies and g-C3N4 as the active sites for TM nanocluster's growth was studied within the framework of density functional theory. Both thermodynamic and kinetic aspects of composite synthesis were discussed. It was found that potential barriers of adatom's migration from bigraphene's outer surface to the interlayer space through the double vacancy are rather low values. High potential barriers of TM migration along the carbon plane prevents TM clusterization due to enhanced chemical activity of double vacancies which gives a possibility to capture the surface adatoms. As was shown for the monolayer graphene, the decrease of vacancies concentration reduces the barrier of adatom migration along the surface while the second graphene sheet in bigraphene stabilizes the structure. The behavior of TM-atom regarding g-CN2 and g-CN1 nanosheets was investigated. Potential energy surfaces were obtained and discussed. The migration barriers were found surmountable that means high probability of migration of TM adatoms to global minima and formation of TM vacancies. Comparison of barriers values with Boltzmann factor demonstrated that just standalone temperature fluctuations cannot initiate structural transitions. The properties of designed structures can be of interest of catalysts and biosensors for biomedical applications.

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Kyungpook National University, 80 Daehakro, Bukgu, Daegu, 41566, South Korea
Siberian Federal University, 79 Svobodny Pr., Krasnoyarsk, 660041, Russian Federation
Tomsk State University, 36 Lenin Ave., Tomsk, 634050, Russian Federation
Kirensky Institute of Physics, FRC KSC SB RAS, 50 Akademgorodok, Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Melchakova, I.; Nikolaeva, K. M.; Kovaleva, E. A.; Tomilin, F. N.; Томилин, Феликс Николаевич; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич; Tchaikovskaya, O. N.; Avramov, P. V.; Kuzubov, A. A.
}
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13.


   
    Polar anchoring energy and tilt angle measured by magneto-optical technique in nematic doped with ionic surfactant / A. M. Parshin, V. S. Sutormin, V. Y. Zyryanov, V. F. Shabanov // Liq. Cryst. - 2020. - Vol. 47, Is. 12. - P. 1825-1831, DOI 10.1080/02678292.2020.1733683. - Cited References: 32 . - ISSN 0267-8292. - ISSN 1366-5855
   Перевод заглавия: Полярная энергия сцепления и угол наклона измеренные магнитооптической методикой в нематике допированном ионным сурфактантом
РУБ Chemistry, Multidisciplinary + Crystallography + Materials Science, Multidisciplinary
Рубрики:
LIQUID-CRYSTAL
   TEMPERATURE-DEPENDENCE

   INTERFACE

   ADSORPTION

Кл.слова (ненормированные):
Nematic -- ionic surfactant -- tilt angle -- anchoring energy -- magnetooptics
Аннотация: The surface anchoring of a nematic doped with the ionic surfactant has been investigated and compared with the one in the undoped sample. The director tilt angle at the substrates coated with the orienting polymer film has been determined by the null method in a rotating magnetic field. The Frederiks transition in a magnetic field has been chosen as a convenient technique to measure the polar anchoring energy Wθ. The temperature dependences of anchoring energy have been obtained for the various nematic cells. The Wθ values for nematic doped with the ionic surfactant are less than for the undoped one. The factors affecting the measurement accuracy have been discussed. The accuracy is higher for the thinner nematic layers and weaker anchoring energy.

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Держатели документа:
Russian Acad Sci, Siberian Branch, Fed Res Ctr,Krasnoyarsk Sci Ctr, Kirensky Inst Phys, Krasnoyarsk, Russia.
Siberian Fed Univ, Krasnoyarsk, Russia.

Доп.точки доступа:
Parshin, A. M.; Паршин, Александр Михайлович; Sutormin, V. S.; Сутормин, Виталий Сергеевич; Zyryanov, V. Ya.; Зырянов, Виктор Яковлевич; Shabanov, V. F.; Шабанов, Василий Филиппович
}
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14.


   
    Physical principles of the formation of a nanoparticle electric double layer in metal hydrosols / A. P. Gavrilyuk [et al.] // Colloid Polym. Sci. - 2020. - Vol. 298, Is. 1. - P. 1-7, DOI 10.1007/s00396-019-04573-8. - Cited References: 25. - The reported research was funded by the Russian Foundation for Basic Research and the government of the Krasnoyarsk territory, Krasnoyarsk Regional Fund of Science, grant No 18-42-243023, the RF Ministry of Education and Science, the State contract with Siberian Federal University for scientific research in 2017–2019. . - ISSN 0303-402X. - ISSN 1435-1536
Кл.слова (ненормированные):
Nanoparticle -- Adsorption layer -- Elastic deformation -- Coagulation kinetics -- Elasticity modulus
Аннотация: The Brownian dynamics method is employed to study the formation of an electrical double layer (EDL) on the metal nanoparticle (NP) surface in hydrosols during adsorption of electrolyte ions from the interparticle medium. Also studied is the charge accumulation by NPs in the Stern layer. To simulate the process of the formation of EDL, we took into account the effect of image forces and specific adsorption, dissipative and random forces, and the degree of hydration of adsorbed ions on the EDL structure. The employed model makes it possible to determine the charge of NPs and the structure of EDL. For the first time, the charge of both the diffuse part of EDL and the dense Stern layer has been determined. A decrease in the electrolyte concentration (below c ˂ 0.1 mol/l) has been found to result in dramatic changes in the formation of the Stern layer.

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Держатели документа:
Institute of Computational Modeling SB RAS, Krasnoyarsk, Russia
Siberian Federal University, Krasnoyarsk, Russia
L. V. Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, Russia
Siberian State University of Science and Technology, Krasnoyarsk, Russia

Доп.точки доступа:
Gavrilyuk, A. P.; Isaev, I. L.; Gerasimov, V. S.; Герасимов, Валерий Сергеевич; Karpov, S. V.; Карпов, Сергей Васильевич
}
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15.


    Parshin, A. M.
    The director field distribution with the strongly pinned alignment in nematic structures at the polymer surface / A. M. Parshin, V. Y. Zyryanov, V. F. Shabanov // Liq. Cryst. - 2015. - Vol. 42, Is. 1. - P. 57-64, DOI 10.1080/02678292.2014.960904. - Cited References:18. - This work was partially supported by the Russian Foundation for BasicResearch [project No. 12-03-00816] and by the Siberian Branch of theRussian Academy of Sciences (SB RAS) [grants nos. 30, 24.29, 24.32] andby SB RAS through a Taiwan-SB RAS joint project. . - ISSN 0267. - ISSN 1366-5855
   Перевод заглавия: Распределение поля директора с сильно фиксированным упорядочением в нематических структурах на поверхности полимера
РУБ Chemistry, Multidisciplinary + Crystallography + Materials Science,
Рубрики:
LIQUID-CRYSTALS
   DISCLINATION LINES

   DEFECTS

Кл.слова (ненормированные):
orientational order -- disclination -- adsorption -- nematic -- polymer surface -- director configuration
Аннотация: We investigate orientational nematic liquid crystal structures that form at the polymer surface due to adsorption, their stability against the schlieren texture and features of point and linear singularities in them. We demonstrate that surface disclination lines, which also occur due to molecular adsorption, can lead to azimuthal anchoring of a bulk layer and make the singularities with the charge m=+/- 1 stable. We consider the director field distribution in a nematic layer as a result of the combination of two aligning factors, which are the linear disclination that tend to impose uniform planar ordering and point defects that impart the radial configuration to the director. With the use of the calculation, we analyse the energies of elastic distortions of the director field for the radial-planar, radial-homeotropic and radial-radial configurations, depending on the nematic layer thickness.

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Держатели документа:
Russian Acad Sci, LV Kirensky Phys Inst, Krasnoyarsk Sci Ctr, Siberian Branch, Krasnoyarsk, Russia.
Siberian Fed Univ, Dept Energy, Krasnoyarsk, Russia.

Доп.точки доступа:
Zyryanov, V. Ya.; Зырянов, Виктор Яковлевич; Shabanov, V. F.; Шабанов, Василий Филиппович; Паршин, Александр Михайлович; Russian Foundation for Basic Research [12-03-00816]; Siberian Branch ofthe Russian Academy of Sciences (SB RAS) [30, 24.29, 24.32]; SB RASthrough a Taiwan-SB RAS joint project
}
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16.


   
    Oxidation of Ag nanoparticles in aqueous media: Effect of particle size and capping / Y. L. Mikhlin [et al.] // Appl. Surf. Sci. - 2014. - Vol. 297. - P. 75-83, DOI 10.1016/j.apsusc.2014.01.081. - Cited References: 58. - This work was partially financially supported by the Ministry of Education and Science of RF (Grant 8580) and RFBR (12-03-31178). . - ISSN 0169-4332. - ISSN 1873-5584
   Перевод заглавия: Окисление наночастиц Ag в водной среде: Влияние размера частиц и оболочки.
РУБ Chemistry, Physical + Materials Science, Coatings & Films + Physics, Applied + Physics, Condensed Matter
Рубрики:
EX-SITU XPS
   POLYCRYSTALLINE SILVER ELECTRODES

   RAY PHOTOELECTRON-SPECTROSCOPY

   METAL NANOPARTICLES

   ELECTROCHEMICAL OXIDATION

   ABSORPTION SPECTROSCOPY

   PYROLYTIC-GRAPHITE

   OXYGEN-ADSORPTION

   TRANSFORMATIONS

   DISSOLUTION

Кл.слова (ненормированные):
Silver nanoparticles -- Oxidation -- Resistive switching effect -- X-ray photoelectron spectroscopy
Аннотация: Many applications and environmental impact of silver-bearing nanomaterials critically depend upon their specific reactivity, which is still poorly understood. Here, silver nanoparticles (Ag NPs) of about 3-5 nm and 10-12 nm in diameter, uncapped and capped with l-glucose or citrate, were prepared, characterized using UV-vis absorption spectroscopy, SAXS, TEM, and their (electro) chemical oxidation was examined in comparison with each other and bulk metal applying scanning tunneling microscopy and spectroscopy, cyclic voltammetry, and XPS. A resistive switching effect was found in the tunneling spectra measured in air at the smaller uncapped Ag NPs deposited on HOPG and was interpreted in terms of Ag transfer between the particle and the probe. The anodic oxidation of these Ag NPs in 1 M NaOH yielded 3D Ag2O, while only a layer of "primary"Ag(I) oxide emerged on larger uncapped nanoparticles during the potential sweep. The formation of AgO at higher potentials proceeded readily at the "primary"oxide but was retarded at the smaller NPs. The citrate- and glucose-capping substantially impeded the formation both of Ag2O and AgO. The findings highlighted, particularly, a non-trivial effect of particle size and transient mobilization of Ag species on the reactions of silver nanoparticles. (c) 2014 Elsevier B.V. All rights reserved.

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Держатели документа:
Russian Acad Sci, Siberian Branch, Inst Chem & Chem Technol, Krasnoyarsk 660036, Russia
Siberian Fed Univ, Krasnoyarsk 660041, Russia
Russian Acad Sci, Siberian Branch, Boreskov Inst Catalysis, Novosibirsk 630090, Russia
Russian Acad Sci, Siberian Branch, Kirensky Inst Phys, Krasnoyarsk 660036, Russia

Доп.точки доступа:
Mikhlin, Y. L.; Vishnyakova, E. A.; Romanchenko, A. S.; Saikova, S. V.; Сайкова, С. В.; Likhatski, M. N.; Larichev, Y. V.; Tuzikov, F. V.; Zaikovskii, V. I.; Zharkov, S. M.; Жарков, Сергей Михайлович
}
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17.


   
    On the nature of citrate-derived surface species on Ag nanoparticles: Insights from X-ray photoelectron spectroscopy / Y. L. Mikhlin [et al.] // Appl. Surf. Sci. - 2018. - Vol. 427. - P. 687-694, DOI 10.1016/j.apsusc.2017.09.026. - Cited References: 50. - We thank the Russian-German bilateral program “Russian-German laboratory at BESSY II” and the staff of the RGLab and HZB for their kind assistance with XANES experiments. . - ISSN 0169-4332
   Перевод заглавия: Исследования методом фотоэлектронной рентгеновской спектроскопии адсорбатов на поверхности наночастиц Ag
Кл.слова (ненормированные):
Silver nanoparticles -- Adsorption -- Citrate capping -- X-ray photoelectron spectroscopy
Аннотация: Citrate is an important stabilizing, reducing, and complexing reagent in the wet chemical synthesis of nanoparticles of silver and other metals, however, the exact nature of adsorbates, and its mechanism of action are still uncertain. Here, we applied X-ray photoelectron spectroscopy, soft X-ray absorption near-edge spectroscopy, and other techniques in order to determine the surface composition and to specify the citrate-related species at Ag nanoparticles immobilized from the dense hydrosol prepared using room-temperature reduction of aqueous Ag+ ions with ferrous ions and citrate as stabilizer (Carey Lea method). It was found that, contrary to the common view, the species adsorbed on the Ag nanoparticles are, in large part, products of citrate decomposition comprising an alcohol group and one or two carboxylate bound to the surface Ag, and minor unbound carboxylate group; these may also be mixtures of citrate with lower molecular weight anions. No ketone groups were specified, and very minor surface Ag(I) and Fe (mainly, ferric oxyhydroxides) species were detected. Moreover, the adsorbates were different at AgNPs having various size and shape. The relation between the capping and the particle growth, colloidal stability of the high-concentration sol and properties of AgNPs is briefly considered. © 2017 Elsevier B.V.

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Держатели документа:
Institute of Chemistry and Chemical Technology of the Siberian Branch of the Russian Academy of Sciences, Akademgorodok 50/24, Krasnoyarsk, Russian Federation
Siberian Federal University, Svobodny av. 79, Krasnoyarsk, Russian Federation
Department of Chemistry and The Smalley-Curl Institute, Rice University, 6100 Main Street, Houston, United States
Kirensky Institute of Physics of the Siberian Branch of the Russian Academy of Sciences, Akademgorodok 50/38, Krasnoyarsk, Russian Federation
Boreskov Institute of Catalysis of the Siberian Branch of the Russian Academy of Sciences, Lavrent’, ev av. 5, Novosibirsk, Russian Federation

Доп.точки доступа:
Mikhlin, Y. L.; Vorobyev, S. A.; Saikova, S. V.; Vishnyakova, E. A.; Romanchenko, A. S.; Zharkov, S. M.; Жарков, Сергей Михайлович; Larichev, Y. V.
}
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18.


   
    Modification of synthetic valleriite surface with gold nanoparticles: The roles of specific adsorption and zeta potential / A. A. Karacharov, M. N. Likhatski, R. V. Borisov [et al.] // Colloid J. - 2024. - Vol. 86, Is. 1. - P. 40-51, DOI 10.1134/S1061933X23601075. - Cited References: 69. - This work was supported by the Russian Science Foundation project no. 22-13-00321 . - ISSN 1061-933X. - ISSN 1608-3067
Кл.слова (ненормированные):
synthetic valleriites -- gold nanoparticles -- X-ray photoelectron spectroscopy -- transmission electron microscopy -- zeta potential
Аннотация: Layered two-dimensional materials, whose properties dramatically differ from their bulk precursors, are of great theoretical and applied importance. Recently, a layered 2D material, an analog of a natural mineral, valleriite, in which quasi-monoatomic Cu−Fe−S sheets alternate with brucite-like ones, has been prepared using a simple hydrothermal synthesis procedure. The features of the electronic structure of these materials make it possible to propose them as new materials for a wide field of applications such as (electro)photocatalysis, high-capacity batteries, etc. In this work, nanocomposite materials have been prepared via immobilization of gold nanoparticles (AuNPs) from citrate hydrosols on the surface of the synthesized valleriites having different compositions of hydroxide layers, which control the surface charge density. According to X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), energy-dispersive X-ray microanalysis (EDX), and selected area electron diffraction (SAED) data, AuNPs are immobilized on valleriite nanoflakes, which have lateral sizes of 150–200 nm and thicknesses of several tens of nanometers, as isolated metal nanoparticles with an average diameter of 11 nm. A small amount of aggregates indicates a high affinity of AuNPs for the valleriite surface. The amounts of immobilized gold are the same on all studied valleriites (~0.2%). This finding may be related to the simultaneous sorption of free citrate ions from the AuNP hydrosols, with these ions, according to zeta potential measurements, charging the surfaces of all studied valleriite samples to nearly the same negative value of –40 mV. According to the XPS data, the AuNPs immobilization markedly decreases the magnesium and oxygen contents on the surfaces of the synthesized valleriites due to the partial degradation/dissolution of the brucite layer. In addition, the amount of Fe3+ ions bound to OH groups decreases with a simultaneous increase in the fraction of Fe3+–O species. The TEM data have confirmed the preservation of the layered structure of valleriites after the immobilization of AuNPs.

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Публикация на русском языке Модификация поверхности синтетического валлериита наночастицами золота: роль специфической адсорбции и дзета-потенциала [Текст] / А. А. Карачаров, М. Н. Лихацкий, Р. В. Борисов [и др.]. - 13 с. // Коллоид. журн. - 2024. - Т. 86 № 1. - С. 45-57

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

Доп.точки доступа:
Karacharov, A. A.; Likhatski, M. N.; Borisov, R. V.; Tomashevich, E. V.; Vorobyev, S. A.; Zharkov, S. M.; Жарков, Сергей Михайлович
}
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19.


   
    Magnetic Resonance Imaging of Water Absorption by Highly Porous Ceramic Materials / E. V. Morozov [et al.] // Dokl. Chem. - 2019. - Vol. 484, Is. 2. - P. 44-47, DOI 10.1134/S0012500819020058. - Cited References: 9. - The studies were performed using equipment of KRTsKP FITs "KNTs SO RAN" in the framework of the program of basic research of the Russian Academy of Sciences (project no. V.44.1.7.) regarding the development of the MRI methodology for studying composite and porous materials, and also supported by the Russian Foundation for Basic Research (project no. 16-29-05334ofi_m "Scientific foundations for creating thin-film coatings with controlled wettability") regarding the development of water-repellent porous materials. . - ISSN 0012-5008
Кл.слова (ненормированные):
magnetic resonance imaging -- porosity -- ceramic materials -- hydrophobic coatings -- adsorption -- capillary phenomena
Аннотация: A nontrivial character of water absorption in highly porous ceramic materials has been demonstrated for the first time by magnetic resonance imaging: a phenomenon of hygroscopic memory has been detected consisting in the concentration of adsorbed water in certain areas inside the sample, repeated during subsequent wetting with water. It has been shown that hydrophobization of the material by applying fluoro paraffin coatings to oxide fibers using the method of dissolution of fluoropolymers in supercritical CO2 has a significant impact on the transport of water into products and can be considered an efficient means of protecting porous materials from moisture. The results demonstrate the capabilities of the MRI method in studying the water absorption and identifying water migration pathways in highly porous materials.

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Публикация на русском языке Магнитно-резонансная томография водопоглощения высокопористыми керамическими материалами [Текст] / Е. В. Морозов [и др.] // Докл. Акад. наук. - 2019. - Т. 484 № 5. - С. 563-567

Держатели документа:
Institute of Chemistry and Chemical Technology, Siberian Branch, Russian Academy of Sciences, Krasnoyarsk, 660036, Russian Federation
Kirenskii Institute of Physics, Siberian Branch, Russian Academy of Sciences, Krasnoyarsk, 660036, Russian Federation
All-Russian Research Institute of Aviation Materials, Moscow, 105005, Russian Federation
Gubkin State University of Oil and Gas, Moscow, 119991, Russian Federation

Доп.точки доступа:
Morozov, E. V.; Морозов, Евгений Владимирович; Buznik, V. M.; Bespalov, A. S.; Grashchenkov, D. V.
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    Magnetic nanoparticles Fe3O4, Fe3O4@sIo2, Fe3O4@C, and Fe3O4@C@C for the organic dyes adsorption / O. S. Ivanova, I. S. Edelman, A. Е. Sokolov [et al.] // VIII Euro-Asian symposium "Trends in magnetism" (EASTMAG-2022) : Book of abstracts / program com. S. G. Ovchinnikov [et al.]. - 2022. - Vol. 2, Sect. M : Magnetism in biology and medicine. - Ст. M.O4. - P. 424-436. - Cited References: 1. - Support by Ministry of Science and Technology of Taiwan, Grants MOST № 108-2923-M-153-001-MY3 and № 109-2112-M-153-003- is acknowledged . - ISBN 978-5-94469-051-7

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Держатели документа:
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, Russia
National Pingtung University, Pingtung City, Taiwan

Доп.точки доступа:
Ivanova, O. S.; Иванова, Оксана Станиславовна; Edelman, I. S.; Эдельман, Ирина Самсоновна; Sokolov, A. Е.; Соколов, Алексей Эдуардович; Svetlitsky, E. S.; Chun-Rong Lin; Ying-Zhen Chen; Российская академия наук; Физико-технический институт им. Е.К. Завойского ФИЦ Казанского научного центра РАН; Казанский (Приволжский) федеральный университет; Euro-Asian Symposium "Trends in MAGnetism"(8 ; 2022 ; Aug. ; 22-26 ; Kazan); "Trends in MAGnetism", Euro-Asian Symposium(8 ; 2022 ; Aug. ; 22-26 ; Kazan)
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