Eduard Karakhanov

Prof. Eduard Karakhanov

Lomonosov Moscow State University, Faculty of Chemistry, Department of petroleum chemistry and organic catalysis, GSP-1, 1-3 Leninskiye Gory, 119991 Moscow, Russia.

Research Focus & Metrics

Academic Career Length

27Years (2000-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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5 January 2016 in Reaction Kinetics, Mechanisms and Catalysis
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Journal Article
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Anton Lvovich MaksimovAnton Lvovich Maksimov
Anton Lvovich Maksimov
AZAnna Zolotukhina
Anna Zolotukhina
LKLeonid Kulikov
Leonid Kulikov
YKYulia Kardasheva
Yulia Kardasheva
Eduard KarakhanovEduard Karakhanov
Eduard Karakhanov

12 November 2015 in Chemistry and Technology of Fuels and Oils
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Journal Article
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SES. V. Egazar’yants
S. V. Egazar’yants
VVVladimir Vinokurov
Vladimir Vinokurov
AVA. V. Vutolkina
A. V. Vutolkina
MTM. Yu. Talanova
M. Yu. Talanova
VFV. I. Frolov
V. I. Frolov
Eduard KarakhanovEduard Karakhanov
Eduard Karakhanov

12 March 2015 in ChemCatChem
Verified
Journal Article
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Anton Lvovich MaksimovAnton Lvovich Maksimov
Anton Lvovich Maksimov
AZAnna Zolotukhina
Anna Zolotukhina
VMVadim Murzin
Vadim Murzin
Eduard KarakhanovEduard Karakhanov
Eduard Karakhanov
EREdward Rosenberg
Edward Rosenberg

1 August 2021 in Applied Catalysis A: General
Verified
Journal Article
Closed access
GDGorbunov Dmitry
Gorbunov Dmitry
MNMaria Nenasheva
Maria Nenasheva
Evgeny NaranovEvgeny Naranov
Evgeny Naranov
Anton Lvovich MaksimovAnton Lvovich Maksimov
Anton Lvovich Maksimov
EREdward Rosenberg
Edward Rosenberg
Eduard KarakhanovEduard Karakhanov
Eduard Karakhanov

1 January 2022 in Petroleum Chemistry
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Journal Article
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GDGorbunov Dmitry
Gorbunov Dmitry
MNMaria Nenasheva
Maria Nenasheva
MTMaria Terenina
Maria Terenina
YKYulia Kardasheva
Yulia Kardasheva
SKS. V. Kardashev
S. V. Kardashev
Eduard KarakhanovEduard Karakhanov
Eduard Karakhanov
In view of the growing environmental concerns and the need to involve alternative sources of raw materials in the chemical industry, intensive research efforts in the last decades have focused on carbon dioxide reactions. In this context, the present review discusses prior studies that were aimed at producing commercially important compounds, such as acids, alcohols, organic carbonates, and polycarbonates, in homogeneous catalytic systems that contain transition-metal complexes. Such systems have been traditionally valued for their high activity and selectivity under relatively mild conditions. The review provides systematized information both on CO2 reactions with hydrogen to produce C1 chemicals such as formic acid and methanol, and on CO2 interactions with organics (e.g., olefins, alcohols, and epoxides) to produce valuable chemical compounds.

13 May 2020 in Catalysts
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Journal Article
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AGAleksandr Glotov
Aleksandr Glotov
AVAnna Vutolkina
Anna Vutolkina
APAleksey Pimerzin
Aleksey Pimerzin
VNVladimir Nedolivko
Vladimir Nedolivko
GZGleb Zasypalov
Gleb Zasypalov
VVVladimir Vinokurov
Vladimir Vinokurov
Mesoporous ruthenium catalysts (0.74–3.06 wt%) based on ordered Mobil Composition of Matter No. 41 (MCM-41) silica arrays on aluminosilicate halloysite nanotubes (HNTs), as well as HNT-based counterparts, were synthesized and tested in benzene hydrogenation. The structure of HNT core-shell silica composite-supported Ru catalysts were investigated by transmission electron microscopy (TEM), X-ray fluorescence (XRF) and temperature-programmed reduction (TPR-H2). The textural characteristics were specified by low-temperature nitrogen adsorption/desorption. The catalytic evaluation of Ru nanoparticles supported on both the pristine HNTs and MCM-41/HNT composite in benzene hydrogenation was carried out in a Parr multiple reactor system with batch stirred reactors (autoclaves) at 80 °C, a hydrogen pressure of 3.0 MPa and a hydrogen/benzene molar ratio of 3.3. Due to its hierarchical structure and high specific surface area, the MCM-41/HNT composite provided the uniform distribution and stabilization of Ru nanoparticles (NPs) resulted in the higher specific activity and stability as compared with the HNT-based counterpart. The highest specific activity (5594 h−1) along with deep benzene hydrogenation to cyclohexane was achieved for the Ru/MCM-41/HNT catalyst with a low metal content.