Kinetics of a monomolecular reaction between n components

1980 ◽  
Vol 45 (4) ◽  
pp. 1197-1220 ◽  
Author(s):  
Jaromír Jakeš

The reaction kinetics has been investigated of a general monomolecular reaction between n components, where reactions between some components are reversible and between others irreversible. The reacting components may be divided into groups so that all the components inside one group may change reversibly into each other, while reactions between components of different groups are irreversible. The reaction kinetics for each reversible group may be found similarly to the case where all the reactions are reversible; solutions for the individual reversible groups may be used to obtain solution for the whole system. A solution was also found to a difficult case in which matrices have multiple eigenvalues for irreversible consecutive reactions, namely, for a general case of degeneracy. Formulas are given for the calculation of derivatives of concentrations of the individual components with respect to parameters. The equations thus derived were applied to the reaction kinetics of a polymeranalogous reaction (e.g., hydrolysis of polyacrylonitrile).

1979 ◽  
Vol 44 (4) ◽  
pp. 1146-1159 ◽  
Author(s):  
Jaromír Jakeš

It has been shown that the solution of kinetic equations can be transformed into diagonalization of a symmetrical matrix, in contrast with the solution known so far and requiring diagonalization of a nonsymmetrical matrix. Simple formulas are given for the calculation of derivatives of the concentrations of individual components with respect to the parameters. All formulas are presented in a compact matrix form; their uniformity for a large number of cases recognized in the existing literature greatly facilitates writing computer programs for calculations of reaction kinetics.


1986 ◽  
Vol 51 (12) ◽  
pp. 2786-2797
Author(s):  
František Grambal ◽  
Jan Lasovský

Kinetics of formation of 1,2,4-oxadiazoles from 24 substitution derivatives of O-benzoylbenzamidoxime have been studied in sulphuric acid and aqueous ethanol media. It has been found that this medium requires introduction of the Hammett H0 function instead of the pH scale beginning as low as from 0.1% solutions of mineral acids. Effects of the acid concentration, ionic strength, and temperature on the reaction rate and on the kinetic isotope effect have been followed. From these dependences and from polar effects of substituents it was concluded that along with the cyclization to 1,2,4-oxadiazoles there proceeds hydrolysis to benzamidoxime and benzoic acid. The reaction is thermodynamically controlled by the acid-base equilibrium of the O-benzylated benzamidoximes.


1983 ◽  
Vol 14 (17) ◽  
Author(s):  
L. I. SVYATKINA ◽  
N. D. ABRAMOVA ◽  
L. L. DMITRIEVA ◽  
B. V. TRZHTSINSKAYA ◽  
G. G. SKVORTSOVA

1994 ◽  
Vol 105 (2) ◽  
pp. 169-176 ◽  
Author(s):  
Nancy L. Pochopin ◽  
William N. Charman ◽  
Valentino J. Stella

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