440. The kinetics of catalytic polymerizatios. Part III. The kinetics and mechanism of the polymerization of α-methylstyrene catalyzed by aluminium chloride

1952 ◽  
Vol 0 (0) ◽  
pp. 2354-2358 ◽  
Author(s):  
D. O. Jordan ◽  
A. R. Mathieson
Keyword(s):  
Kinetics And Mechanism ◽  
Aluminium Chloride ◽  
Kinetics Of

Kinetics and mechanism of the reaction of iron(III) with 6-methyl-2,4-heptanedione and 3,5-heptanedione

1990 ◽  
Vol 55 (8) ◽  
pp. 1984-1990 ◽  
Author(s):  
José M. Hernando ◽  
Olimpio Montero ◽  
Carlos Blanco
Keyword(s):  
Aqueous Solution ◽  
Metal Ion ◽  
Activation Parameters ◽  
Enol Form ◽  
Kinetics And Mechanism ◽  
Kinetic Constants ◽  
Steric Factors ◽  
Kinetics Of ◽  
Mechanism Of The Reaction

The kinetics of the reactions of iron(III) with 6-methyl-2,4-heptanedione and 3,5-heptanedione to form the corresponding monocomplexes have been studied spectrophotometrically in the range 5 °C to 16 °C at I 25 mol l-1 in aqueous solution. In the proposed mechanism for the two complexes, the enol form reacts with the metal ion by parallel acid-independent and inverse-acid paths. The kinetic constants for both pathways have been calculated at five temperatures. Activation parameters have also been calculated. The results are consistent with an associative activation for Fe(H2O)63+ and dissociative activation for Fe(H2O)5(OH)2+. The differences in the results for the complexes of heptanediones studied are interpreted in terms of steric factors.

Kinetics of aluminium deposition from aluminium chloride—alkali chloride melts

1982 ◽  
Vol 27 (11) ◽  
pp. 1595-1598 ◽  
Author(s):  
R. Ødegard ◽  
A. Bjørgum ◽  
Å. Sterten ◽  
J. Thonstad ◽  
R. Tunold
Keyword(s):  
Aluminium Chloride ◽  
Alkali Chloride ◽  
Chloride Melts ◽  
Kinetics Of

scholarly journals Non-isothermal TGA study on the combustion reaction kinetics and mechanism of low-rank coal char

RSC Advances ◽  
2018 ◽  
Vol 8 (41) ◽  
pp. 22909-22916 ◽  
Author(s):  
Yingjie Hu ◽  
Zhiqiang Wang ◽  
Xingxing Cheng ◽  
Chunyuan Ma
Keyword(s):  
Thermal Analysis ◽  
Reaction Kinetics ◽  
Coal Char ◽  
Kinetics And Mechanism ◽  
Combustion Reaction ◽  
Low Rank ◽  
Low Rank Coal ◽  
Pyrolytic Char ◽  
Kinetics Of

The combustion reaction kinetics of pyrolytic char of low-rank coal was investigated by using thermal analysis technology.

Kinetics and mechanism of disproportionation and ferricyanide oxidation of the 10-methylacridinium cation in aqueous base

1984 ◽  
Vol 62 (4) ◽  
pp. 729-735 ◽  
Author(s):  
John W. Bunting ◽  
Glenn M. Kauffman
Keyword(s):  
Ionic Strength ◽  
Second Order ◽  
Kinetics And Mechanism ◽  
Oxidation Pathway ◽  
First Order ◽  
Aqueous Base ◽  
Ph Range ◽  
Rate Profile ◽  
Kinetics Of ◽  
Major Oxidation

The kinetics of disproportionation and ferricyanide ion oxidation of the 10-methylacridinium cation have been measured spectrophotometrically over the pH range 9–14 in.20% CH3CN – 80% H2O (v/v) and ionic strength 1.0 at 25 °C. Disproportionation is kinetically second-order in total acridine species. The pH–rate profile is consistent with the rate-determining reaction of one acridinium cation with the pseudobase alkoxide anion derived from a second acridinium cation. Ferricyanide ion oxidation is kinetically first-order in each of ferricyanide ion and total acridine species. The pH–rate profile requires three distinct pathways for the ferricyanide ion oxidation of the 10-methylacridinium cation. For pH < 9.7, rate-determining attack of ferricyanide ion on the neutral pseudobase predominates, while for pH > 12.8 the predominant oxidation pathway involves reaction of ferricyanide ion with the pseudobase alkoxide ion. Between pH 9.7 and 12.8, the major oxidation pathway involves initial disproportionation of the acridinium cation followed by ferricyanide ion oxidation of the 9,10-dihydro-10-methylacridine product. This latter route accounts for a maximum of 69% of the total ferricyanide ion oxidation at pH 11.1.

scholarly journals A study of the kinetics and mechanism of rabbit muscle l-glycerol 3-phosphate dehydrogenase

1974 ◽  
Vol 143 (1) ◽  
pp. 19-27 ◽  
Author(s):  
Philip Bentley ◽  
F. Mark Dickinson
Keyword(s):  
Basic Mechanism ◽  
Kinetics And Mechanism ◽  
Dihydroxyacetone Phosphate ◽  
Rabbit Muscle ◽  
Kinetics Of Oxidation ◽  
Mechanism Of Catalysis ◽  
Glycerol 3 Phosphate Dehydrogenase ◽  
Ph Range ◽  
Kinetics Of

1. The kinetics of oxidation of l-glycerol 3-phosphate by NAD+and of reduction of dihydroxyacetone phosphate by NADH catalysed by rabbit muscle glycerol 3-phosphate dehydrogenase were studied over the range pH6–9. 2. The enzyme was found to catalyse the oxidation of glyoxylate by NAD+at pH8.0 and the kinetics of this reaction were also studied. 3. The results are consistent with a compulsory mechanism of catalysis for glycerol 3-phosphate oxidation and dihydroxyacetone phosphate reduction in the intermediate regions of pH, but modifications to the basic mechanism are required to fully explain results at the extremes of the pH range, with these substrates and for glyoxylate oxidation at pH8.0.

The kinetics and mechanism of solvent extraction of Pr(iii) from chloride medium in the presence of two complexing agents with di-(2-ethylhexyl) phosphoric acid

RSC Advances ◽  
2015 ◽  
Vol 5 (60) ◽  
pp. 48659-48664 ◽  
Author(s):  
Shao-Hua Yin ◽  
Shi-Wei Li ◽  
Jin-Hui Peng ◽  
Li-Bo Zhang
Keyword(s):  
Lactic Acid ◽  
Citric Acid ◽  
Solvent Extraction ◽  
Phosphoric Acid ◽  
Interfacial Area ◽  
Kinetics And Mechanism ◽  
Complexing Agents ◽  
Extraction Kinetics ◽  
Chloride Medium ◽  
Kinetics Of

The extraction kinetics of Pr(iii) from chloride medium containing two complexing agents lactic acid (HLac) and citric acid (H3cit) with di-(2-ethylhexyl)phosphoric acid (D2EHPA, H2A2) have been investigated by constant interfacial area cell with lamina flow.

scholarly journals Pyrolysis of azetidinones. Part 2. Kinetics and mechanism of thermolysis of β-lactams and β-thiolactams

2016 ◽  
Vol 94 (9) ◽  
pp. 788-793 ◽  
Author(s):  
Nouf S. Al-Hamdan ◽  
Alya M. Al-Etaibi ◽  
Rasha F. Al-Bashir ◽  
Yahia A. Ibrahim ◽  
Nouria A. Al-Awadi ◽  
...  
Keyword(s):  
Gas Phase ◽  
Rate Constants ◽  
Kinetics And Mechanism ◽  
Energy Of Activation ◽  
The Novel ◽  
Temperature Range ◽  
Entropy Of Activation ◽  
Kinetics Of ◽  
Thermolysis Reaction

The kinetics of the gas-phase thermolysis reaction of seven β-lactams and their thione analogues were investigated over the temperature range 533–603 K for the β-lactams and 463–542 K for the β-thiolactams. The average values of the energy of activation (Ea) (kJ mol−1) and Arrhenius log A (s–1) were, respectively, 170.8 ± 18.6 and 12.4 ± 1.6 for the lactams and 131.7 ± 18.2 and 11.0 ± 2.0 for the thione analogues. The entropy of activation (ΔS#) was negative for of the substrates and slightly positive for three. The rate constants (k) (s−1) were calculated for 510 K and compared for the two series of azetidinones. The effects of substituents on rates and the novel role played by the C=O and C=S moieties on the relative reactivities of the cyclic amides are rationalized on the basis of a formal retro[2+2]cycloaddition mechanism used earlier to explain the products of the gas-phase thermolysis reaction of the present azetidinones.

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