Thermodynamic activation parameters for the rhodium complex catalyzed carbonylation of primary alcohols

1978 ◽  
Vol 4 (3) ◽  
pp. 199-203 ◽  
Author(s):  
Jes Hjortkjaer ◽  
J.C. Aerbo Jørgensen
Keyword(s):  
Activation Parameters ◽  
Rhodium Complex ◽  
Primary Alcohols ◽  
Thermodynamic Activation Parameters

Kinetic Studies of [4n+2]π-Thermal Cyclodimerization of 1-(3-Pyridazinyl)-3-oxidopyridinium Betaines

1992 ◽  
Vol 57 (9) ◽  
pp. 1951-1959 ◽  
Author(s):  
Madlene L. Iskander ◽  
Samia A. El-Abbady ◽  
Alyaa A. Shalaby ◽  
Ahmed H. Moustafa
Keyword(s):  
Energy Gap ◽  
Activation Parameters ◽  
Kinetic Studies ◽  
Cyclic Transition ◽  
Concerted Mechanism ◽  
First Order ◽  
Thermodynamic Activation Parameters ◽  
Cyclic Transition State ◽  
Complete Dissociation ◽  
Homo Lumo

The reactivity of the base induced cyclodimerization of 1-(6-arylpyridazin-3-yl)-3-oxidopyridinium chlorides in a pericyclic process have been investigated kinetically at λ 380 nm. The reaction was found to be second order with respect to the liberated betaine and zero order with respect to the base. On the other hand dedimerization (monomer formation) was found to be first order. It was shown that dimerization is favoured at low temperature, whereas dedimerization process is favoured at relatively high temperature (ca 70 °C). Solvent effects on the reaction rate have been found to follow the order ethanol > chloroform ≈ 1,2-dichloroethane. Complete dissociation was accomplished only in 1,2-dichloroethane at ca 70 °C. The thermodynamic activation parameters have been calculated by a standard method. Thus, ∆G# has been found to be independent on substituents and solvents. The high negative values of ∆S# supports the cyclic transition state which is in favour with the concerted mechanism. MO calculations using SCF-PPP approximation method indicated low HOMO-LUMO energy gap of the investigated betaines.

Kinetic Study of the Oxidation of Alcohols with Quaternary Ammonium Permanganates

1993 ◽  
Vol 58 (8) ◽  
pp. 1777-1781 ◽  
Author(s):  
Robert Šumichrast ◽  
Vladislav Holba
Keyword(s):  
Kinetic Study ◽  
Catalytic Reaction ◽  
Rate Constants ◽  
Quaternary Ammonium ◽  
Iterative Procedure ◽  
Activation Parameters ◽  
Reaction Products ◽  
Thermodynamic Activation Parameters ◽  
Oxidation Of Alcohols ◽  
Kinetics Of

Kinetics of the oxidation of 2-propanol, 1-butanol, and 1-pentanol with tetraalkylammonium permanganates have been investigated as function of temperature. The studied reactions are partly autocatalytic, colloidal manganese dioxide as one of the reaction products has been identified as the autocatalyst.A computerized iterative procedure has been used in order to obtained the rate constants of both non-catalytic and catalytic reaction steps together with the thermodynamic activation parameters.

scholarly journals Kinetics and Mechanism of Oxidation of Diethanolamine and Triethanolamine by Potassium Ferrate

2011 ◽  
Vol 8 (2) ◽  
pp. 903-909 ◽  
Author(s):  
Shan Jinhuan ◽  
Zhang Jiying
Keyword(s):  
Activation Parameters ◽  
Rate Equations ◽  
Potassium Ferrate ◽  
Kinetics Of Oxidation ◽  
First Order ◽  
Order Dependence ◽  
Rate Determining Step ◽  
Thermodynamic Activation Parameters ◽  
Plausible Mechanism ◽  
Kinetics Of

The kinetics of oxidation of diethanolamine and triethanolamine by potassium ferrate(VI)in alkaline liquids at a constant ionic strength has been studied spectrophotometrically in the temperature range of 278.2K-293.2K. The reaction shows first order dependence on potassium ferrate(VI), first order dependence on each reductant, The observed rate constant (kobs) decreases with the increase in [OH-], the reaction is negative fraction order with respect to [OH-]. A plausible mechanism is proposed and the rate equations derived from the mechanism can explain all the experimental results. The rate constants of the rate-determining step and the thermodynamic activation parameters are calculated.

Kinetics of oxidation of cis-bis(ethylenediamine)isothiocyanatonitrocobalt(III) ion with peroxodisulphate

1979 ◽  
Vol 44 (12) ◽  
pp. 3588-3594 ◽  
Author(s):  
Vladislav Holba ◽  
Olga Volárová
Keyword(s):  
Ionic Strength ◽  
Rate Constants ◽  
Oxidation Kinetics ◽  
Reaction Rate ◽  
Salt Effect ◽  
Activation Parameters ◽  
Reaction Products ◽  
Kinetics Of Oxidation ◽  
Thermodynamic Activation Parameters ◽  
Kinetics Of

The oxidation kinetics of cis-bis(ethylenediamine)isothiocyanonitrocobalt(III) ion with peroxodisulphate was investigated in the medium of 0.01 M-HClO4 in dependence on the ionic strength and temperature and the reaction products were identified. Extrapolated values of thermodynamic activation parameters were determined from the temperature dependence of the rate constants extrapolated to zero ionic strength. The distance of the closest approach was estimated for the reacting ions by evaluating the primary salt effect. To elucidate the mechanism, the influence of the cyclic polyether 18-crown-6 on the reaction rate was followed.

scholarly journals Comparative Evaluation of Anticorrosive Properties of Mahaleb Seed Extract on Carbon Steel in Two Acidic Solutions

Materials ◽  
2019 ◽  
Vol 12 (18) ◽  
pp. 3013 ◽  
Author(s):  
Aisha A. Ganash
Keyword(s):  
Carbon Steel ◽  
Inhibition Efficiency ◽  
Electrochemical Impedance ◽  
Activation Parameters ◽  
Protection Mechanism ◽  
Acidic Solutions ◽  
Langmuir Adsorption ◽  
Thermodynamic Activation Parameters ◽  
Green Corrosion Inhibitor

Aqueous extract solution of Mahaleb seed (ASMS) was prepared using a simple and safe method. ASMS was tested to examine its potential to act as a green corrosion inhibitor for preventing the dissolution of Carbon steel in highly concentrated corrosive 2 M H2SO4 and 2 M H3PO4 using an electrochemical polarization Tafel plot and electrochemical impedance spectroscopy. ASMS provided a slight increase in the inhibition efficiency of H3PO4 (89%) compared with H2SO4 (86%). Fourier transform infrared spectroscopy (FTIR) and electronic scanning microscopy (SEM) were used to prove that adsorption of ASMS occurred on the metal surface. The thermodynamic adsorption and thermodynamic activation parameters were calculated at a range of concentrations and temperatures. The physisorption of ASMS followed the Langmuir adsorption isotherm (R2 = 0.98). Finally, the role of ASMS as a protection mechanism was discussed.

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