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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Воробьев С. А., Лихацкий М. Н., Романченко А. С., Иваненко Т. Ю., Машарова Д. А., Волочаев, Михаил Николаевич, Михлин Ю. Л.
Заглавие : Влияние реакционных условий на размер наночастиц серебра в концентрированных золях Carey Lea
Коллективы : RUSSIAN SCIENCE FOUNDATIONRussian Science Foundation (RSF) [18-73-00142]
Место публикации : Журн. СФУ. Химия. - 2020. - Т. 13, № 3. - С. 372-384. - ISSN 1998-2836, DOI 10.17516/1998-2836-0190; J. Sib. Fed. Univ. Chem. - ISSN 2313-6049(eISSN)
Примечания : Библиогр.: 34. - Работа выполнена при финансовой поддержке Российского научного фонда, грант No 18-73-00142
Предметные рубрики: AG NANOPARTICLES
CITRATE
AGGREGATION
SURFACE
STABILITY
KINETICS
Аннотация: В данной работе был изучен процесс восстановления растворов Ag (I) цитратными комплексами Fe (II), который позволяет получать наночастицы серебра с высокой стабильностью и концентрацией более 60 г/л. В ходе работы было установлено влияние скорости введения, скорости перемешивания, концентрации реагентов, рН среды и некоторых постсинтетических операций на средний размер наночастиц. Показано, что снижение концентрации Ag (I) и повышение концентрации стабилизатора, доведение рН реакционной среды до 7 позволяют получать наиболее мелкие и однородные частицы. В результате были найдены оптимальные условия, которые дали возможность уменьшить размер частиц и вместе с тем снизить концентрацию реактивов на 33 %. По данным РФЭС, ПЭМ, DLS и ИК были получены наночастицы металлического серебра с размером 6.5±1.8 нм, стабилизированные продуктом частичного распада цитрат-иона.The reaction of reduction solution of Ag (I) by Fe (II) citrate complex was studied herein. This allows you to receive silver nanoparticles with high stability with a concentration above 60 g/l. It was determined that the nanoparticles size depends on the injection rate, mixing rate, reagent concentration, pH and some post-synthetic operations on the average size of nanoparticles. It was shown that decreasing the concentration of Ag (I) and increasing the concentration of stabilizer also bringing pH to 7 lead to small and uniform particles. Optimal conditions were found that made it possible to reduce particle size and reduce the concentration of reagents by 33 % in the results. According to XPS, TEM, DLS and FTIR datas, nanoparticles of metallic silver with a size of 6.5±1.8 nm were obtained, which stabilized by the product of partial decay of the citrate ion.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Zharkov S. M., Altunin R. R., Yumashev V. V., Moiseenko E. T., Belousov O. V., Solovyov L. A., Volochaev M. N., Zeer G. M.
Заглавие : Kinetic study of a solid-state reaction in Ag/Al multilayer thin films by in situ electron diffraction and simultaneous thermal analysis
Коллективы : Russian Science Foundation, RussiaRussian Science Foundation (RSF) [181300 080]
Место публикации : J. Alloys Compd. - 2021. - Vol. 871. - Ст.159474. - ISSN 0925-8388, DOI 10.1016/j.jallcom.2021.159474. - ISSN 1873-4669(eISSN)
Примечания : Cited References: 47. - This work was supported by the Russian Science Foundation, Russia under grant #181300 080
Предметные рубрики: STRUCTURAL PHASE-TRANSFORMATIONS
COMMITTEE RECOMMENDATIONS
ICTAC KINETICS
Аннотация: A solid-state reaction process in Ag/Al multilayer thin films has been investigated by the methods of in situ electron diffraction, simultaneous thermal analysis, transmission electron microscopy and X-ray diffraction with the aim of studying the phase formation kinetics of intermetallic compounds. The sequence of the phase transformations in the solid-state reaction has been established: Ag+Al→(Ag)+(Al)→(Ag)+δ-Ag2Al→μ-Ag3Al. The process of the solid-state interaction has been shown to consist of two steps; each of them is described by a kinetic model of the nth order reactions with autocatalysis. The kinetic parameters of the autocatalytic process of the phase formation for δ-Ag2Al and µ-Ag3Al, have been determined, in particular, their apparent activation energy: 126 kJ/mol and 106 kJ/mol, respectively.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Potylitsyna, Arina R., Mishakov, Ilya, V, Bauman, Yury, I, Kibis, Lidia S., Shubin, Yury, V, Volochaev M. N., Melgunov, Maxim S., Vedyagin, Aleksey A.
Заглавие : Metal dusting as a key route to produce functionalized carbon nanofibers
Коллективы : Ministry of Science and Higher Education of the Russian Federation [AAAA-A21-121011390054-1, 0239-2021-0010, 121031700315-2]
Место публикации : React. Kinet. Mech. Catal. - 2022. - Vol. 135, Is. 3. - P.1387-1404. - ISSN 1878-5190, DOI 10.1007/s11144-022-02169-y. - ISSN 1878-5204(eISSN)
Примечания : Cited References: 65. - This work was supported by the Ministry of Science and Higher Education of the Russian Federation (Project numbers AAAA-A21-121011390054-1 (ID: 0239-2021-0010) and 121031700315-2)
Предметные рубрики: CHLORINATED HYDROCARBONS
NI-CU
DECOMPOSITION
NANOTUBES
CATALYST
Аннотация: The present paper reports a new method of producing N-doped carbon nanofibers via metal dusting of a ternary NiMoW alloy in the atmosphere containing C2HCl3 and CH3CN vapors at 600 °C. The initial alloy was prepared by a co-precipitation technique. The carbon deposition was monitored gravimetrically. The early stages of the metal dusting process were studied in detail using scanning and transmission electron microscopies. It was established that the rapid disintegration of the microdispersed NiMoW alloy with the formation of nanosized particles catalyzing the growth of carbon filaments occurs within the first 5 min of the reaction. The presence of C2HCl3 vapors in the reaction medium was shown to be the urgent condition to provide efficient metal dusting. The effect of the CH3CN concentration in the trichloroethylene-containing reaction mixture on the carbon deposition is investigated. As observed, the CH3CN content noticeable affects the carbon yield (after 2 h of reaction). The dome-shaped dependence of carbon yield reaches its maximal value of ~ 200 g/g(cat) at a CH3CN concentration of 33 vol%. According to X-ray photoelectron spectroscopy, the obtained carbon filaments are functionalized with Cl (0.1–1.2 wt%), O (3–6 wt%), and N (0.5–1.3 wt%). The prepared carbon filaments possess a segmented secondary structure, which is typical for carbon nanomaterials derived via catalytic decomposition of chlorine-substituted hydrocarbons. Low-temperature nitrogen adsorption measurement revealed that the specific surface area of the N-containing samples varies in a range from 370 to 550 m2/g.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Chen M., Nong S., Zhao Y., Riaz M. S., Xiao Y., Molokeev M. S., Huang F.
Заглавие : Renewable P-type zeolite for superior absorption of heavy metals: Isotherms, kinetics, and mechanism
Место публикации : Sci. Total Environ. - 2020. - Vol. 726. - Ст.138535. - ISSN 00489697 (ISSN), DOI 10.1016/j.scitotenv.2020.138535
Примечания : Cited References: 47. - This work was supported by the National Key Research and Development Program of China (Grant No. 2016YFB0901600 ); National Science Foundation of China (Grant No. 21871008 ); Science and Technology Commission of Shanghai Municipality (Grant No. 14520722000 ) and China Postdoctoral Science Foundation [Grant No. 8206300161 ]. Thank Shuying Nong for her experimental assistance
Аннотация: Zeolite is a characteristic material for removing heavy metals exhibiting by low tolerance quantities. It is particularly desirable although challenging to cultivate an unmodified and reusable zeolite for eradicating heavy metals with great capacity. Herein, we sought out and firstly synthesized the uniform octahedral zeolite Na6Al6Si10O32·12H2O for heavy metal ions trap, proven extraordinarily effective decontamination of M2+ (Pb2+, Cd2+, Cu2+, and Zn2+). The maximum capacities of Pb2+, Cd2+, Cu2+, and Zn2+ were 649, 210, 90 and 88 mg/g, and the distribution coefficients (Kd) was ~108 mL/g for Pb2+ which emphasized the superior effectiveness of Na6Al6Si10O32·12H2O contrasted with other zeolites. Rapid adsorption was observed that Pb2+ concentration (7.5 ppm) was reduced to 0.6 ppb in 2 min. The removal mechanism was ascribed to the ion exchange and hydroxyl groups thereby affording high adsorption capacity. We also investigated the heavy metal removal of zeolite 13X and 4A for comparison and concluded the determining factor affecting absorption capacity. The removal rate of Pb remained at 97% even after five regeneration recycles. The zeolite was therefore promising for practical water purification and industrialization.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Gavrilyuk A. P., Isaev I. L., Gerasimov V. S., Karpov S. V.
Заглавие : Physical principles of the formation of a nanoparticle electric double layer in metal hydrosols
Место публикации : Colloid Polym. Sci. - 2020. - Vol. 298, Is. 1. - P.1-7. - ISSN 0303-402X, DOI 10.1007/s00396-019-04573-8. - ISSN 1435-1536 (eISSN)
Примечания : 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.
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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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Chzhan A. V., Podorozhnyak S. A., Patrin G. S., Rudenko R. Yu., Onufrienok V. V.
Заглавие : Influence of solution acidity on growth kinetics, structure and magnetic properties of Co-P films, obtained by chemical deposition
Коллективы : Euro-Asian Symposium "Trends in MAGnetism"
Место публикации : J. Phys. Conf. Ser. - 2019. - Vol. 1389, Is. 1. - Ст.012116. - ISSN 1742-6588, DOI 10.1088/1742-6596/1389/1/012116. - ISSN 1742-6596 (eISSN)
Примечания : Cited References: 21
Аннотация: The results of studies of the effect of solution acidity on the growth kinetics, structure and magnetic properties of Co-P films obtained by chemical deposition are presented. It was shown that the growth of Co-P films in the low pH region occurs mainly due to the growth of crystallite sizes, and in the high pH region, due to an increase in the nucleation rate. From the analysis of the chemical equilibrium of redox reactions, taking into account the balance of citrate and hydroxyl complexes of Co, a qualitative explanation of the features of the change in the rate and nature of the deposition of Co atoms from pH is proposed.
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Вид документа : Статья из сборника (однотомник)
Шифр издания :
Автор(ы) : Chzhan A. V., Podorozhnyak S. A., Rudenko R. Yu.
Заглавие : Influence of solid acidity on growth kinetics, structure and magnetic properties of CoP films during chemical deposition
Коллективы : Российская академия наук, Уральское отделение РАН, Институт физики металлов им. М. Н. Михеева Уральского отделения РАН, Уральский федеральный университет им. первого Президента России Б.Н. Ельцина, Российский фонд фундаментальных исследований, Euro-Asian Symposium "Trends in MAGnetism", "Trends in MAGnetism", Euro-Asian Symposium
Место публикации : Euro-asian symposium "Trends in magnetism" (EASTMAG-2019): Book of abstracts/ чл. конс. ком.: S. G. Ovchinnikov, N. V. Volkov [et al.] ; чл. прогр. ком. D. M. Dzebisashvili [et al.]. - 2019. - Vol. 2. - Ст.J.P38. - P.254-255. - ISBN 978-5-9500855-7-4 (Шифр В33/E12-125657784)
Примечания : Cited References: 3
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Volova, Tatiana G., Demidenko, Aleksey V., Murueva, Anastasiya V., Dudaev, Alexey E., Nemtsev I. V., Shishatskaya, Ekaterina I.
Заглавие : Biodegradable polyhydroxyalkanoates formed by 3- and 4-hydroxybutyrate monomers to produce nanomembranes suitable for drug delivery and cell culture
Колич.характеристики :23 с
Место публикации : Technologies. - 2023. - Vol. 11, Is. 4. - Ст.106. - ISSN 22277080 (eISSN), DOI 10.3390/technologies11040106
Примечания : Cited References: 116. - his research was funded by State Assignment of the Ministry of Science and Higher Education of the Russian Federation (project No. 0287-2021-0025)
Аннотация: Biodegradable polyhydroxyalkanoates, biopolymers of microbiological origin, formed by 3- and 4-hydroxybutyrate monomers P(3HB-co-4HB), were used to obtain nanomembranes loaded with drugs as cell carriers by electrospinning. Resorbable non-woven membranes from P(3HB-co-4HB) loaded with ceftazidime, doripinem, and actovegin have been obtained. The loading of membranes with drugs differently affected the size of fibers and the structure of membranes, and in all cases increased the hydrophilicity of the surface. The release of drugs in vitro was gradual, which corresponded to the Higuchi and Korsmeyer-Peppas models. Antibiotic-loaded membranes showed antibacterial activity against S. aureus and E. coli, in which growth inhibition zones were 41.7 ± 1.1 and 38.6 ± 1.7 mm for ceftazidime and doripinem, respectively. The study of the biological activity of membranes in the NIH 3T3 mouse fibroblast culture based on the results of DAPI and FITC staining of cells, as well as the MTT test, did not reveal a negative effect despite the presence of antibiotics in them. Samples containing actovegin exhibit a stimulating effect on fibroblasts. Biodegradable polyhydroxyalkanoates formed by 3-hydroxybutyrate and 4-hydroxybutyrate monomers provide electrospinning non-woven membranes suitable for long-term delivery of drugs and cultivation of eukaryotic cells, and are promising for the treatment of wound defects complicated by infection.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Basova S. A., Molokeev M. S., Oreshonkov A. S., Zhernakov M. A., Khritokhin N. A., Aleksandrovsky A. S., Krylov A. S., Sal’nikova E. I., Azarapin N. O., Shelpakova N. A., Muller-Buschbaum K., Denisenko Yu. G.
Заглавие : Thermochemistry, structure, and optical properties of a new β-La2(SO4)3 polymorphic modification
Колич.характеристики :14 с
Место публикации : Inorganics. - 2023. - Vol. 11, Is. 11. - Ст.434. - ISSN 23046740 (eISSN), DOI 10.3390/inorganics11110434
Примечания : Cited References: 58. - The work was partly carried out within the framework of the Strategic Academic Leadership Program “Priority-2030” for the Kazan Federal University and the state assignment of the Kirensky Institute of PhysicsWe acknowledge Lisa-Marie Wagner (JLU Giessen) for help with X-ray powder diffractometry, and Svetlana Volkova and Irina Palamarchuk (UTMN) for help with IR- and UV-spectrometry. The use of equipment provided by the Krasnoyarsk Regional Center of Research Equipment of Federal Research Center “Krasnoyarsk Science Center SB RAS” is acknowledged
Аннотация: A new polymorphic modification of lanthanum sulfate was obtained by thermal dehydration of the respective nonahydrate. According to powder X-ray diffraction, it was established that β-La2(SO4)3 crystallized in the C2/c space group of the monoclinic system with the KTh2(PO4)3 structure type (a = 17.6923(9), b = 6.9102(4), c = 8.3990(5) Å, β = 100.321(3)°, and V = 1010.22(9) Å3). Temperature dependency studies of the unit cell parameters indicated almost zero expansion along the a direction in the temperature range of 300–450 K. Presumably, this occurred due to stretching of the [LaO9]n chains along the c direction, which occurred without a significant alteration in the layer thickness over the a direction. A systematic study of the formation and destruction processes of the lanthanum sulfates under heating was carried out. In particular, the decisive impact of the chemical composition and formation energy of compounds on the thermodynamic and kinetic parameters of the processes was established. DFT calculations showed β-La2(SO4)3 to be a dielectric material with a bandgap of more than 6.4 eV. The processing of β-La2(SO4)3 with the Kubelka–Munk function exhibited low values below 6.4 eV, which indicated a fundamental absorption edge above this energy that was consistent with LDA calculations. The Raman and infrared measurements of β-La2(SO4)3 were in accordance with the calculated spectra, indicating that the obtained crystal parameters represented a reliable structure.
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10.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Zharkov S. M., Yumashev V. V., Moiseenko E. T., Altunin R. R., Solovyov L. A., Volochaev M. N., Zeer G. M., Nikolaeva N. S., Belousov O. V.
Заглавие : Thermokinetic study of aluminum-induced crystallization of a-Si: The effect of Al layer thickness
Колич.характеристики :24 с
Место публикации : Nanomaterials. - 2023. - Vol. 13, Is. 22. - Ст.2925. - ISSN 20794991 (eISSN), DOI 10.3390/nano13222925
Примечания : Cited References: 70. - This work was supported by the Russian Science Foundation under grant #22-13-00313
Аннотация: The effect of the aluminum layer on the kinetics and mechanism of aluminum-induced crystallization (AIC) of amorphous silicon (a-Si) in (Al/a-Si)n multilayered films was studied using a complex of in situ methods (simultaneous thermal analysis, transmission electron microscopy, electron diffraction, and four-point probe resistance measurement) and ex situ methods (X-ray diffraction and optical microscopy). An increase in the thickness of the aluminum layer from 10 to 80 nm was found to result in a decrease in the value of the apparent activation energy Ea of silicon crystallization from 137 to 117 kJ/mol (as estimated by the Kissinger method) as well as an increase in the crystallization heat from 12.3 to 16.0 kJ/(mol Si). The detailed kinetic analysis showed that the change in the thickness of an individual Al layer could lead to a qualitative change in the mechanism of aluminum-induced silicon crystallization: with the thickness of Al ≤ 20 nm. The process followed two parallel routes described by the n-th order reaction equation with autocatalysis (Cn-X) and the Avrami–Erofeev equation (An): with an increase in the thickness of Al ≥ 40 nm, the process occurred in two consecutive steps. The first one can be described by the n-th order reaction equation with autocatalysis (Cn-X), and the second one can be described by the n-th order reaction equation (Fn). The change in the mechanism of amorphous silicon crystallization was assumed to be due to the influence of the degree of Al defects at the initial state on the kinetics of the crystallization process.
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