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  • 1
    Electronic Resource
    Electronic Resource
    Evaluation of reforming catalyst activity in integral reactor (1986)
    Springer
    Chemistry and technology of fuels and oils 22 (1986), S. 526-530 
    Details
    ISSN: 1573-8310
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00727118
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Kinetic studies of Pt/Al2O3 catalyst pellets with nonuniform activity (1984)
    Springer
    Reaction kinetics and catalysis letters 26 (1984), S. 279-284 
    Details
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Abstract Изучены катализаторы с неравномерным распределением активного компонента (Pt) по эерну носителя (Al2O3). Показано, что неравномерное распределение активности приводит не только к изменению наблюдаемой скоростн на зерне, но и кинетический законометхостей самой реакции.
    Notes: Abstract Catalysts with nonuniform distribution of the catalytically active component (Pt) over their porous support (Al2O3) have been studied. A nonuniform activity distribution changes not only the reaction rate but also the kinetics can be different on these catalysts.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02067850
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  • 3
    Electronic Resource
    Electronic Resource
    Catalytic properties of metallic and electron-deficient platinum in reforming over Pt/Al2O3 catalysts (1988)
    Springer
    Reaction kinetics and catalysis letters 37 (1988), S. 457-462 
    Details
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Abstract Исследована активность катализаторов с различным содержанием металлической (Pto) и электронодефицитной (Ptσ) платины в реакциях дегидроциклизации н-гептана и дегидрирования циклогексана. Показано, что активность в дегидроциклизации пропорциональна числу поверхностных атомов Ptσ, а в дегидрировании — поверхности металлической платины Pto.
    Notes: Abstract The activity of Pt/Al2O3 catalysts with various contents of metallic (Pto) and electron-deficient (Ptσ) platinum has been examined in dehydrocyclization of n-heptane and dehydrogenation of cyclohexane. In the former case it is proportional to the number of surface Ptσ atoms and in the latter case it is proportional to the BET surface of metallic platinum Pto.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02062099
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  • 4
    Electronic Resource
    Electronic Resource
    Kinetic equation for catalyst deactivation (1989)
    Springer
    Reaction kinetics and catalysis letters 39 (1989), S. 287-292 
    Details
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Abstract Предложено общее кинетическое описание дезактивации, отражающее механизмы целевой реакции и реакции дезактивации. В качестве примера дана реакция реформинга гептана с закоксовыванием катализатора.
    Notes: Abstract Proposed is a general form of the kinetic description of catalytic reaction with deactivation. This description takes into account mechanisms of both main and deactivation reactions. Heptane reforming accompanied by catalyst coking is considered as an example.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02071341
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  • 5
    Electronic Resource
    Electronic Resource
    Contribution of electron-deficient platinum to benzene hydrogenation and its activation by water (1989)
    Springer
    Reaction kinetics and catalysis letters 40 (1989), S. 131-136 
    Details
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Abstract Исследована активность металлической (Pto) и электронодефицитной (Ptσ) платины Pt/Al2O3-катализаторов в низкотемпературном гидрировании бензола. Определена кинетика реакции. Показано, что предадсорбция воды не меняет вид кинетической зависимости, но приводит к увеличению скорости реакции за счет роста удельной активности Ptσ.
    Notes: Abstract The activity of metallic (Pto) and electron-deficient (Ptσ) platinum in Pt/Al2O3 catalysts has been studied in the low temperature hydrogenation of benzene. Reaction kinetics has been clarified. It is shown that water preadsorption does not affect the character of kinetic curves, but enhances the reaction rate due to an increase in the specific activity of Ptσ.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02235151
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  • 6
    Electronic Resource
    Electronic Resource
    Deactivation of reforming catalysts. Coke formation on metallic and acidic centers (1990)
    Springer
    Reaction kinetics and catalysis letters 41 (1990), S. 277-282 
    Details
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Abstract Для контроля закоксования металлических (Pto) и кислотных (Al3+) центров катализаторов Pt/Al2O3 и Pt−Sn/Al2O3 обосновано использование ИК-спектроскопии адсорбированного CO с детектированием связей Pto−CO (2070 см−1) и Al3+−CO (2190 см−1). Показано, что снижение числа активных центров Pto коррелирует с уменьшением скорости дегидрирования циклогексана, а Al3+-изомеризации гептана.
    Notes: Abstract To check coke formation on metallic (Pto) and acidic (Al3+) centers of Pt/Al2O3 and Pt−Sn/Al2O3 catalysts, the application of IR spectroscopy of adsorbed CO for detecting Pto−CO (2070 cm−1) and Al3+−CO (2190 cm−1) bonds has been substantiated. Decrease in the number of active Pto and Al3+ centers is shown to correlate with that in the dehydrogenation rate of cyclohexane and in the isomerization rate of heptane, respectively.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02097881
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  • 7
    Electronic Resource
    Electronic Resource
    Catalytic reactions accompanied by capillary condensation. 1. Formulation of the problems (1994)
    Springer
    Reaction kinetics and catalysis letters 53 (1994), S. 253-259 
    Details
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Capillary condensation was found to accompany gasphase catalytic reactions, in particular motor fuel hydrotreatment. Reaction conditions appear to differ significantly in large pores (filled with gas) and small ones (filled with liquid). Regarding capillary condensation we explain the “strange” dependences observed in this study or described in the literature. We have simulated jet fuel dearomatization taking into account capillary condensation as well.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02073028
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  • 8
    Electronic Resource
    Electronic Resource
    Catalytic reaction accompanied by capillary condensation, 3. Influence on reaction kinetics and dynamics (1998)
    Springer
    Reaction kinetics and catalysis letters 65 (1998), S. 321-329 
    Details
    ISSN: 1588-2837
    Keywords: Catalytic reaction ; capillary condensation ; kinetics ; dynamics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The influence of capillary condensation of reagents on the catalytic reaction kinetics and dynamics was studied. The hydrogenation ofp-xylene over Pt/SiO2 was used as a model reaction. Two types of SiO2 were used (KCK-1 with large pores and KCM-5 with small pores). It was shown that capillary condensation could modify the kinetics and the transition regimes. The proposed mathematical model demonstrates good agreement with experimental results for both steady-state and dynamic regimes, including reaction rate—temperature hysteresis.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02475271
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    Paper (German National Licenses)
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  • 9
    Electronic Resource
    Electronic Resource
    Catalytic reactions accompanied by capillary condensation 2. Mass transfer inside a pellet (1995)
    Springer
    Reaction kinetics and catalysis letters 56 (1995), S. 391-399 
    Details
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The influence of mass transfer inside a catalyst pellet is analyzed in the case when a catalytic reaction accompanied by capillary condensation takes place. It is shown that gas-liquid interfacial transfer as well as diffusion in the liquid does not limit the process. The overall rate is determined by diffusion in “macropores” filled with gas, or by the reaction rate in the liquid phase.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02076045
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    Paper (German National Licenses)
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  • 10
    Electronic Resource
    Electronic Resource
    Distribution of the active component among pores of different size (microdistribution) (1996)
    Springer
    Reaction kinetics and catalysis letters 58 (1996), S. 161-168 
    Details
    ISSN: 1588-2837
    Keywords: Catalytic reactions ; active component distribution
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The role of active component distribution among the pores of different size in supported catalysts has been examined. The influence of “microdistribution” on catalyst pellet activity and stability were studied. It was shown that the “microdistribution” parameter does not affect the pellet effectiveness factor in the case of gas-phase reactions. High catalyst stability can be achieved when the fraction of “micropores” does not exceed 30–40%, otherwise the deactivation rate constants in small and large pores differ less than 5 times.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02071120
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