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1.
Teleshev A. T. Vasil"eva L. N. Nifant"ev E. E. Tsodikov M. V. Bukhtenko O. V. Zhdanova T. N. 《Russian Chemical Bulletin》2003,52(9):2083-2085
The reactivities of cyclophosphite precursors in alkoxo syntheses involving titanium(iv) tetra(n-butoxide) were studied by 31P NMR and IR spectroscopy. 2-Diethylamido-4-methyl-1,3,2-dioxaphosphinane and 4-ethyl-2,6,7-trioxaphosphabicyclo[2.2.2]octane in benzene are inert toward Ti(OBu)4. Gelation is accompanied by hydrolysis 2-diethylamido-4-methyl-1,3,2-dioxaphosphinane to give the corresponding hydrophosphoryl compound, while 4-ethyl-2,6,7-trioxaphosphabicyclo[2.2.2]octane remains intact during gelation. 相似文献
2.
E. Yu. Liberman A. V. Naumkin A. A. Revina A. I. Mikhailichenko M. V. Tsodikov S. A. Medvedeva T. V. Kon’kova 《High Energy Chemistry》2018,52(4):307-311
The effect of electron-beam irradiation on the catalytic properties of PdO/CeO2 has been examined. It has been found that irradiation in the range of 15–30 kGy results in an increase in the concentration of the radical anion [O?], thereby enhancing the catalytic activity of PdO/CeO2. 相似文献
3.
A. V. Chistyakov M. A. Gubanov V. Yu. Murzin P. A. Zharova M. V. Tsodikov V. V. Kriventsov A. E. Gekhman I. I. Moiseev 《Russian Chemical Bulletin》2014,63(1):88-93
The features of ethanol conversion into hydrocarbons C4-C12 in the presence of the novel catalyst Pd-Zn/γ-alumina and pilot zeolite system Pd-Zn/MFI/γ-alumina were studied (MFI is high-siliceous zeolite with ZSM-5 type structure). The structure of active sites changes noticeably in the course of preliminary activation and catalytic reaction. High selectivity and stability of the zeolite-containing Pd-Zn catalyst in alcohol conversion into hydrocarbon components of fuels is related to the stable composition of the alloy that forms clusters PdZn. At the same time, the alumina-based catalyst loses stability due to zinc diffusion from the alloy into γ-Al2O3 to form the spinel structure. 相似文献
4.
The state of the art in production and consumption of carbon sorbents and the main directions of research in this field are considered. Approaches to preparing sorbents derived from lignin are summarized. The advantages and drawbacks of lignin as a raw material and prospects for the progress in this field are discussed. 相似文献
5.
Tsodikov M. V. Slivinskii E. V. Yushchenko V. V. Kitaev L. E. Kriventsov V. V. Kochubei D. I. Teleshev A. T. 《Russian Chemical Bulletin》2000,49(12):2003-2006
The data of temperature-programmed desorption of ammonia from the surface of oxide systems and IR spectroscopy were used to demonstrate that the strength of the surface acid sites in titanium oxides prepared by the alkoxo method and modified by aluminum decreases with respect to that in nonmodified titanium oxide. Modification of titanium oxide with P3+ ions from ethriol phosphite almost completely suppresses the acid properties. Modified oxides are able to chemisorb water. XANES data suggest that modification of titanium oxide with phosphorus ions increases the electron density on the titanium atoms and, correspondingly, the basicity of the materials. 相似文献
6.
A. V. Chistyakov P. A. Zharova M. A. Gubanov S. A. Nikolaev T. B. Egorova A. E. Gekhman M. V. Tsodikov 《Kinetics and Catalysis》2017,58(6):741-748
The results of a study on the activity and operational stability of an Au–Pd/MFI/Al2O3 catalyst in the reaction of ethanol conversion into a gasoline fraction of hydrocarbons are reported. In the presence of the Au–Pd/MFI/Al2O3 catalyst, ethanol was almost completely converted into an alkane–aromatic fraction of C3–C11 hydrocarbons at 300°C in an atmosphere of Ar; the yield of this fraction was as high as 90% on a feed carbon basis. It was established that, in the presence of the bimetallic Au–Pd catalyst, the yield of the target fraction increased by 10%, as compared with that on a monometallic Au-containing sample. The Au–Pd/MFI/Al2O3 catalyst exhibited much higher stability in a long-term experiment in comparison with the previously tested pilot sample of Pd–Zn/MFI/Al2O3. After a 40-h operation, the yield of the target fraction of C3+ hydrocarbons in the presence of the Au–Pd/MFI/Al2O3 catalyst decreased by 15%. The treatment of the catalyst with hydrogen led to the complete restoration of its activity. The structure of the Au–Pd active constituents was studied by transmission electron microscopy X-ray photoelectron spectroscopy. methods of the and microscopy. 相似文献
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9.
V. V. Kriventsov E. P. Yakimchuk B. N. Novgorodov D. I. Kochubey I. L. Simakova D. A. Zyuzin D. G. Aksenov A. V. Chistyakov A. S. Fedotov K. V. Golubev V. Yu. Murzin M. V. Tsodikov 《Bulletin of the Russian Academy of Sciences: Physics》2013,77(9):1190-1194
Model low-percentage metal oxide palladium catalysts are prepared from acetate complexes of Pd and Mn to study the nature of the activity and the genesis of nanostructured membrane catalyst Pd-Mn systems. A comprehensive study of the prepared model precursor compounds; specific features of their metal components in gels and oxides; and the genesis of the active component, local structure, and charge state is performed by EXAFS and XANES. Possible versions of structural models for the stabilization of metals on oxide supports aare discussed. 相似文献
10.
A. V. Chistyakov P. A. Zharova M. V. Tsodikov S. A. Nikolaev I. N. Krotova D. I. Ezzhelenko 《Kinetics and Catalysis》2016,57(6):803-811
The direct conversion of ethanol into the linear primary alcohols C n H2n+1OH (n = 4, 6, and 8) in the presence of the original mono- and bimetallic catalysts Au/Al2O3, Ni/Al2O3, and Au–Ni/Al2O3 was studied. It was established that the rate and selectivity of the reaction performed under the conditions of a supercritical state of ethanol sharply increased in the presence of Au–Ni/Al2O3. The yield of target products on the bimetallic catalyst was higher by a factor of 2–3 than that reached on the monometallic analogs. Differences in the catalytic behaviors of the Au, Ni, and Au–Ni systems were discussed with consideration for their structure peculiarities and reaction mechanisms. 相似文献