Zobrazeno 1 - 10
of 27
pro vyhledávání: '"V. A. Semikolenov"'
Autor:
Sandro Recchia, V. Dal Santo, Rinaldo Psaro, A. V. Golovin, Irina V. Deliy, Nicoletta Ravasio, Nataliya V. Maksimchuk, Eugenii A. Paukshtis, V. A. Semikolenov
Publikováno v:
Applied catalysis. A, General
279 (2005): 99–107. doi:10.1016/j.apcata.2004.10.017
info:cnr-pdr/source/autori:Deliy I.V., Maksimchuk N.M., Psaro R., Ravasio N., Dal Santo V., Recchia S., Paukshtis E.A., Golovin A.V., Semikolenov V.A./titolo:Kinetic peculiarities of cis%2Ftrans methyl oleate formation during hydrogenation of methyl linoleate over Pd%2FMgO/doi:10.1016%2Fj.apcata.2004.10.017/rivista:Applied catalysis. A, General (Print)/anno:2005/pagina_da:99/pagina_a:107/intervallo_pagine:99–107/volume:279
279 (2005): 99–107. doi:10.1016/j.apcata.2004.10.017
info:cnr-pdr/source/autori:Deliy I.V., Maksimchuk N.M., Psaro R., Ravasio N., Dal Santo V., Recchia S., Paukshtis E.A., Golovin A.V., Semikolenov V.A./titolo:Kinetic peculiarities of cis%2Ftrans methyl oleate formation during hydrogenation of methyl linoleate over Pd%2FMgO/doi:10.1016%2Fj.apcata.2004.10.017/rivista:Applied catalysis. A, General (Print)/anno:2005/pagina_da:99/pagina_a:107/intervallo_pagine:99–107/volume:279
Kinetic peculiarities of cis and trans methyl oleate formation in the course of methyl linoleate hydrogenation over Pd/MgO were studied. Liquid phase hydrogenation was carried out in temperature range of 303–323 K and under hydrogen pressure within
Publikováno v:
Applied Catalysis A: General. 272:109-114
Kinetic peculiarities of α-pinene liquid-phase oxidation by molecular oxygen were studied (in a temperature range of 343–393 K and at oxygen pressure within 0.5–6 bar range). The process proceeds selectively at a low α-pinene conversion and the
Publikováno v:
Reaction Kinetics and Catalysis Letters. 82:165-172
Thermal isomerization of verbenol in the gas and liquid phases is discussed. The effect of temperature and residence time on the reaction mixture composition was studied (at 460-600°C and a residence time t of about 10-3 min for the gas phase condit
Publikováno v:
Journal of Molecular Catalysis A: Chemical. :383-393
The regularities of pinane-2-ol isomerization over block catalyst under reagent pressure of 2–45 Torr and within a temperature range of 450–620 °C were studied. A scheme of key product—linalool, as well as side products—hydrocarbons and 5-me
Publikováno v:
Kinetics and Catalysis. 43:645-651
The liquid-phase hydrogenation of α-pinene on a Pd/C catalyst at 0–100°С and hydrogen pressures of 1–11 atm was studied. It was found that the order of reaction with respect to pinene increased with hydrogen pressure and did not depend on temp
Publikováno v:
Kinetics and Catalysis. 43:652-656
The liquid-phase hydrogenation of pinane hydroperoxide (PHP) to pinanol on a Pd/C catalyst at 20–80°C and hydrogen pressures of 1–11 atm was studied. It was found that the rate of hydrogenation decreased with PHP concentration. The rate of PHP h
Publikováno v:
Kinetics and Catalysis. 42:686-692
Isomerization of 2-pinanol into linalool is studied on a monolith carbon-containing catalyst at 733–893 and a total pressure of 2–40 torr. The rate constants of cis(trans)-2-pinanol transformation into linalool and linalool cyclization are determ
Publikováno v:
Kinetics and Catalysis. 42:41-45
The liquid-phase oxidation of pinane to pinane hydroperoxide (PHP) by dioxygen is studied at 353–373 K and under dioxygen pressures ranging from 2 to 4 atm. The rate of pinane oxidation is described by the equation w = w O 2 + w PHP , where the ter
Publikováno v:
Inorganic Materials. 36:591-594
The oxidation resistance of porous carbon materials in air was studied by thermal analysis. The effects that the size, ordering, and orientation of carbon microcrystallites and the curvature of the surface of primary particles have on the temperature
Autor:
Irina L. Simakova, V. A. Semikolenov
Publikováno v:
Kinetics and Catalysis. 41:383-387
A selective catalytic system for the hydrogenation of 1-vinylpyrrolidone-2 (VP) to 1-ethylpyrrolidone-2 (EP) is found. The factors responsible for the formation of by-products in the conversion of VP are studied. The presence of acid sites or radical