Preparation and Evaluation of Skeletal Cobalt-Molybdenum Hydrodesulfurization Catalysts

1995 ◽  
Vol 60 (4) ◽  
pp. 568-575
Author(s):  
Karel Sporka ◽  
Jiří Hanika ◽  
Vladimír Jůn
Keyword(s):  
Aqueous Solutions ◽  
Active Component ◽  
Catalyst Activity ◽  
Gas Oil ◽  
Gamma Alumina ◽  
Molybdenum Sulfides ◽  
Hydrodesulfurization Catalysts ◽  
Hds Catalysts ◽  
Kinetics Of ◽  
Preparation And Evaluation

Preparation of skeletal Co-Mo catalysts by controlled impregnation of aluminosilicate skeletons containing deposited gamma-alumina with aqueous solutions of active component precursors has been investigated. The activity of the laboratory catalysts in gas oil hydrodesulfurization has been determined. Kinetics of impregnation of skeletal supports, the effect of their type, and the dependence of catalyst activity on the content of cobalt and molybdenum sulfides are reported. HDS skeletal catalysts prepared were compared with the extruded types. It was found that skeletal HDS catalysts show the higher activity (related to the content of alumina and Co-Mo sulfides) than the extruded ones due to the less significant effect of internal diffusion. However, if the activity is related to the same volume of catalyst bed, the activity of skeletal catalysts is only one fourth of that of the extruded types.

Development of Cobalt-Molybdenum Hydrodesulfurization Catalysts

1992 ◽  
Vol 57 (12) ◽  
pp. 2501-2508 ◽  
Author(s):  
Karel Sporka ◽  
Jiří Hanika
Keyword(s):  
Aqueous Solutions ◽  
Aromatic Compounds ◽  
Laboratory Scale ◽  
Gas Oil ◽  
Active Components ◽  
Hydrodesulfurization Catalysts ◽  
The Individual ◽  
Kinetics Of

The Co-Mo catalysts have been prepared on laboratory scale by controlled impregnation of extruded γ-alumina with aqueous solutions of suitable active components, and their activity has been tested in the hydrodesulfurization and hydrogenation of aromatic compounds in gas oil. The kinetics of impregnation of the carrier, the effect of its nature, the order of impregnation of precursors of the individual active components, and the effect of their nature on the activity of the catalyst prepared have been studied. The samples prepared have been compared with selected commercial catalysts.

Effects of salts on the kinetics of oxidation of alkenes by thallic salts in aqueous solutions

1981 ◽  
Vol 46 (3) ◽  
pp. 693-700 ◽  
Author(s):  
Milan Strašák ◽  
Jaroslav Majer
Keyword(s):  
Aqueous Solutions ◽  
Phase Transfer ◽  
Heterogeneous Reaction ◽  
Qualitative Model ◽  
Kinetic Effect ◽  
Tetraalkylammonium Salts ◽  
Reaction Conditions ◽  
Kinetics Of Oxidation ◽  
Kinetics Of ◽  
Heterogeneous Reaction Conditions

The kinetics of oxidation of alkenes by thallic sulphate in aqueous solutions, involving the two reaction steps-the hydroxythallation and the dethallation - was studied, and the effect of salts on the kinetics was examined; this made it possible to specify more precisely the reaction mechanism and to suggest a qualitative model of the reaction coordinate. It was found that in homogeneous as well as in heterogeneous reaction conditions, the reaction can be accelerated appreciably by adding tetraalkylammonium salts. These salts not only operate as catalysts of the phase transfer, but also exert a significant kinetic effect, which can be explained with a simplification in terms of a stabilization of the transition state of the reaction.

Kinetics of carbon monoxide methanation on a Ni/SiO2 catalyst

1990 ◽  
Vol 55 (7) ◽  
pp. 1678-1685
Author(s):  
Vladimír Stuchlý ◽  
Karel Klusáček
Keyword(s):  
Carbon Monoxide ◽  
Reaction Rate ◽  
Catalyst Activity ◽  
Adsorbed Hydrogen ◽  
Reaction Products ◽  
Co Methanation ◽  
Molar Ratios ◽  
Rate Determining Step ◽  
Higher Temperature ◽  
Kinetics Of

Kinetics of CO methanation on a commercial Ni/SiO2 catalyst was evaluated at atmospheric pressure, between 528 and 550 K and for hydrogen to carbon monoxide molar ratios ranging from 3 : 1 to 200 : 1. The effect of reaction products on the reaction rate was also examined. Below 550 K, only methane was selectively formed. Above this temperature, the formation of carbon dioxide was also observed. The experimental data could be described by two modified Langmuir-Hinshelwood kinetic models, based on hydrogenation of surface CO by molecularly or by dissociatively adsorbed hydrogen in the rate-determining step. Water reversibly lowered catalyst activity and its effect was more pronounced at higher temperature.

Study of potential oscillations during reaction of an aluminium single crystal with an aqueous KOH solution

1990 ◽  
Vol 55 (2) ◽  
pp. 345-353 ◽  
Author(s):  
Ivan Halaša ◽  
Milica Miadoková
Keyword(s):  
Aqueous Solutions ◽  
Single Crystal ◽  
Single Crystals ◽  
Periodic Potential ◽  
Optimum Conditions ◽  
Potential Oscillations ◽  
Dilute Aqueous Solutions ◽  
Experimental Findings ◽  
Kinetics Of

The authors investigated periodic potential changes measured on oriented sections of Al single crystals during spontaneous dissolution in dilute aqueous solutions of KOH, with the aim to find optimum conditions for the formation of potential oscillations. It was found that this phenomenon is related with the kinetics of the reaction investigated, whose rate also changed periodically. The mechanism of the oscillations is discussed in view of the experimental findings.

Apparent Kinetics of Co‐Gasification of Biomass and Vacuum Gas Oil (VGO)

2020 ◽  
Author(s):  
Tareq A. Al-Attas ◽  
Rahima A. Lucky ◽  
Mohammed Mozahar Hossain
Keyword(s):  
Vacuum Gas Oil ◽  
Gas Oil ◽  
Kinetics Of

Effect of ionic strength on the aggregation kinetics of the amidated amyloid beta peptide Aβ (1-40) in aqueous solutions

2017 ◽  
Vol 228 ◽  
pp. 98-107 ◽  
Author(s):  
Adriana Campos-Ramírez ◽  
Maripaz Márquez ◽  
Liliana Quintanar ◽  
Luis F. Rojas-Ochoa
Keyword(s):  
Ionic Strength ◽  
Aqueous Solutions ◽  
Amyloid Beta ◽  
Amyloid Beta Peptide ◽  
Aggregation Kinetics ◽  
Beta Peptide ◽  
Kinetics Of

The Study of the Kinetics of the Passivation of Nickel in High Temperature Aqueous Solutions

1995 ◽  
Vol 185-188 ◽  
pp. 655-666
Author(s):  
T. Agladze ◽  
G. Tsurtsumia ◽  
I. Khorbaladze ◽  
T. Ekhvaia
Keyword(s):  
High Temperature ◽  
Aqueous Solutions ◽  
Kinetics Of
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