Kinetics of partly diffusion controlled reactions, IX. Cage effect in the photolysis of benzyl chloride in the liquid phase. First results

1981 ◽  
Vol 17 (3-4) ◽  
pp. 433-437 ◽  
Author(s):  
J. C. Andre ◽  
A. Tournier ◽  
M. Bouchy ◽  
X. Deglise
Keyword(s):  
Liquid Phase ◽  
Benzyl Chloride ◽  
Cage Effect ◽  
Diffusion Controlled ◽  
First Results ◽  
Kinetics Of

Effects of Pressure on the Kinetics of Manganese Evaporation from the Ot4 Alloy / Wpływ Cisnienia Na Kinetyke Procesu Odparowania Manganu Ze Stopu Ot4

2013 ◽  
Vol 58 (1) ◽  
pp. 197-201 ◽  
Author(s):  
L. Blacha ◽  
R. Burdzik ◽  
A. Smalcerz ◽  
T. Matuła
Keyword(s):  
Mass Transfer ◽  
Liquid Phase ◽  
Gaseous Phase ◽  
Pressure Range ◽  
Evaporation Rate ◽  
Evaporation Process ◽  
Pressure Reduction ◽  
Diffusion Controlled ◽  
Kinetics Of ◽  
Evaporation Kinetics

In the paper, results of the study on manganese evaporation from the OT4 alloy are presented. In the experiments, the effects of pressure on the manganese evaporation kinetics and the stages that limit the evaporation rate were investigated. It was demonstrated that the rate of manganese evaporation from the alloy increased with pressure reduction in the system. When the pressure decreases from 1000 Pa to 10 Pa, the value of overall mass transfer kMn increases from 3.9*10-6 ms-1 to 208.4*10-6 ms-1. At the same time, the manganese fraction in the alloy decreased from 1.49% mass to 0.045% mass. Within the whole pressure range, the analysed evaporation process is diffusion-controlled. For pressures above 50 Pa, the determining stage is transfer in the gaseous phase, while for pressures below 50 Pa, it is transfer in the liquid phase.

Effect of ionizing radiation on the kinetics of hydrogenation on the Ni-MgO mixed catalyst

1982 ◽  
Vol 47 (7) ◽  
pp. 1780-1786 ◽  
Author(s):  
Rostislav Kudláček ◽  
Jan Lokoč
Keyword(s):  
Experimental Data ◽  
Activation Energy ◽  
Liquid Phase ◽  
Ionizing Radiation ◽  
Oxide Catalyst ◽  
Absorbed Dose ◽  
Hydrogenation Rate ◽  
Solution Composition ◽  
Mixed Catalyst ◽  
Kinetics Of

The effect of gamma pre-irradiation of the mixed nickel-magnesium oxide catalyst on the kinetics of hydrogenation of maleic acid in the liquid phase has been studied. The changes of the hydrogenation rate are compared with the changes of the adsorbed amount of the acid and with the changes of the solution composition, activation energy, and absorbed dose of the ionizing radiation. From this comparison and from the interpretation of the experimental data it can be deduced that two types of centers can be distinguished on the surface of the catalyst under study, namely the sorption centres for the acid and hydrogen and the reaction centres.

Kinetics of esterification of monoisopropylphenols with phosphoryl trichloride

1989 ◽  
Vol 54 (5) ◽  
pp. 1311-1317
Author(s):  
Miroslav Magura ◽  
Ján Vojtko ◽  
Ján Ilavský
Keyword(s):  
Liquid Phase ◽  
Rate Constants ◽  
Reaction Rates ◽  
Activation Energies ◽  
The Individual ◽  
Kinetics Of

The kinetics of liquid-phase isothermal esterification of POCl3 with 2-isopropylphenol and 4-isopropylphenol have been studied within the temperature intervals of 110 to 130 and 90 to 110 °C, respectively. The rate constants and activation energies of the individual steps of this three-step reaction have been calculated from the values measured. The reaction rates of the two isomers markedly differ: at 110 °C 4-isopropylphenol reacts faster by the factors of about 7 and 20 for k1 and k3, respectively. This finding can be utilized in preparation of mixed triaryl phosphates, since the alkylation mixture after reaction of phenol with propene contains an excess of 2-isopropylphenol over 4-isopropylphenol.

The Reactivity of Different Active Forms of Sodium Carbonate with Respect to Sulfur Dioxide

1992 ◽  
Vol 57 (11) ◽  
pp. 2302-2308
Author(s):  
Karel Mocek ◽  
Erich Lippert ◽  
Emerich Erdös
Keyword(s):  
Thermal Decomposition ◽  
Liquid Phase ◽  
Sulfur Dioxide ◽  
Specific Surface ◽  
Surface Area ◽  
Sodium Carbonate ◽  
Room Temperature ◽  
Active Form ◽  
The Other ◽  
Kinetics Of

The kinetics of the reaction of solid sodium carbonate with sulfur dioxide depends on the microstructure of the solid, which in turn is affected by the way and conditions of its preparation. The active form, analogous to that obtained by thermal decomposition of NaHCO3, emerges from the dehydration of Na2CO3 . 10 H2O in a vacuum or its weathering in air at room temperature. The two active forms are porous and have approximately the same specific surface area. Partial hydration of the active Na2CO3 in air at room temperature followed by thermal dehydration does not bring about a significant decrease in reactivity. On the other hand, if the preparation of anhydrous Na2CO3 involves, partly or completely, the liquid phase, the reactivity of the product is substantially lower.

Sign in / Sign up

Export Citation Format

Share Document