Kinetic studies of oxidation–reduction of cobalt–ethylenediaminetetra-acetic acid complexes. Part IV. The reduction of ethylenediaminetetra-acetatocobaltate(III) and related complexes by chromous ion

1966 ◽  
Vol 0 (0) ◽  
pp. 1645-1652 ◽  
Author(s):  
P. B. Wood ◽  
W. C. E. Higginson
Keyword(s):  
Acetic Acid ◽  
Kinetic Studies ◽  
Oxidation Reduction

Degradation of tetracycline antibiotics: Mechanisms and kinetic studies for advanced oxidation/reduction processes

Chemosphere ◽  
2010 ◽  
Vol 78 (5) ◽  
pp. 533-540 ◽  
Author(s):  
Joonseon Jeong ◽  
Weihua Song ◽  
William J. Cooper ◽  
Jinyoung Jung ◽  
John Greaves
Keyword(s):  
Advanced Oxidation ◽  
Kinetic Studies ◽  
Tetracycline Antibiotics ◽  
Reduction Processes ◽  
Oxidation Reduction

scholarly journals Kinetic studies of metalloporphyrin formation. Part I. Mn(II) with hematoporphyrin

1968 ◽  
Vol 46 (22) ◽  
pp. 3431-3436 ◽  
Author(s):  
Doreen A. Brisbin ◽  
Robert J. Balahura
Keyword(s):  
Acetic Acid ◽  
Glacial Acetic Acid ◽  
Kinetic Studies ◽  
Activation Energies ◽  
Kinetics Of

The kinetics of the formation of Mn(III) hematoporphyrin in glacial acetic acid has been studied spectrophotometrically.On addition of Mn(II) to porphyrin in glacial acetic acid a species which appears to be the monocation immediately is formed and is then converted to Mn(III) hematoporphyrin at a rate suitable for kinetic studies.The rates of reaction were measured at 45, 50, and 55 °C and the activation energies were calculated.

scholarly journals Oxidation–reduction reactions of simple hydroxamic acids and plutonium(IV) ions in nitric acid

2008 ◽  
Vol 96 (6) ◽  
Author(s):  
M. J. Carrott ◽  
O. D. Fox ◽  
G. LeGurun ◽  
C. J. Jones ◽  
C. Mason ◽  
...  
Keyword(s):  
Acid Hydrolysis ◽  
Kinetic Studies ◽  
Hydroxamic Acids ◽  
Single Cycle ◽  
Fuel Cycles ◽  
Oxidation Reduction ◽  
Advanced Fuel ◽  
Extraction Processes ◽  
The Stability ◽  
Hydrolysis Of

SummarySimple hydroxamic acids such as formo- and aceto-hydroxamic acids have been proposed as suitable reagents for the separation of either Pu and/or Np from U in modified or single cycle Purex based solvent extraction processes designed to meet the emerging requirements of advanced fuel cycles. The stability of these hydroxamic acids is dominated by their decomposition through acid hydrolysis. Kinetic studies of the acid hydrolysis of formo- and aceto-hydroxamic acids are reported in the absence and the presence of Pu(IV) ions. The slow reduction of these plutonium(IV) hydroxamate complexes to Pu(III) aquo-ions has been characterised by spectrophotometry and cyclic voltammetry. The reductions of Pu(IV) in the presence of FHA and AHA are consistent with a mechanism in which free hydroxamic acid in solution is hydrolysed whilst Pu(IV) ions remain fully complexed to hydroxamate ligands; then at some point close to a 1 : 1 Pu(IV) : XHA ratio, some free Pu

The catalytic oxidation of ethylene on palladium films

1962 ◽  
Vol 270 (1341) ◽  
pp. 219-231 ◽  
Keyword(s):  
Acetic Acid ◽  
Acetic Anhydride ◽  
High Pressures ◽  
Kinetic Studies ◽  
Side Reaction ◽  
Reaction Scheme ◽  
Zero Order ◽  
Main Reaction ◽  
Rate Of Reaction ◽  
Low Pressures

The oxidation of ethylene has been studied on evaporated films of palladium in the temperature range 50 to 140 °C, and products were analyzed by means of a mass spectrometer. The main reaction was complete oxidation to carbon dioxide and water, but trace amounts of acetic anhydride and acetic acid were formed by a side reaction. Kinetic studies showed that the reaction was zero order with respect to the pressure of oxygen, first order in ethylene at low pressures but zero order at high pressures, and progressively poisoned by the two minor products. The activation energy associated with the initial rate of reaction was 14 kcal/mole. A number of subsidiary experiments were carried out including the oxidation of acetaldehyde at 77 °C which occurred rapidly producing acetic anhydride and some acetic acid. A reaction scheme was developed which accounted for the detailed kinetic behaviour of the oxidation of ethylene and possible mechanisms are discussed

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