Physico-chemical aspects of polyethylene processing in an open mixer. Part 9: complements to the experimental kinetics of oxidation product formation

2005 ◽  
Vol 87 (2) ◽  
pp. 231-243 ◽  
Author(s):  
F. Gugumus
Keyword(s):  
Oxidation Product ◽  
Product Formation ◽  
Kinetics Of Oxidation ◽  
Physico Chemical ◽  
Experimental Kinetics ◽  
Kinetics Of

Kinetics of oxidation-product formation in highly refined fuels

1973 ◽  
Vol 9 (9) ◽  
pp. 720-723
Author(s):  
V. A. Astaf'ev ◽  
B. A. �nglin ◽  
V. V. Malyshev ◽  
R. R. Aliev ◽  
V. D. Borisov ◽  
...  
Keyword(s):  
Oxidation Product ◽  
Product Formation ◽  
Kinetics Of Oxidation ◽  
Kinetics Of

scholarly journals Kinetics and Mechanism of Oxidation ofL-Cystine by Hexacyanoferrate(III) in Alkaline Medium

2009 ◽  
Vol 6 (1) ◽  
pp. 93-98 ◽  
Author(s):  
Annapurna Nowduri ◽  
Kalyan Kumar Adari ◽  
Nageswara Rao Gollapalli ◽  
Vani Parvataneni
Keyword(s):  
Alkaline Medium ◽  
Oxidation Product ◽  
Experimental Results ◽  
Cysteic Acid ◽  
Kinetics Of Oxidation ◽  
First Order ◽  
Order Dependence ◽  
Plausible Mechanism ◽  
Mechanism Of Oxidation ◽  
Kinetics Of

Kinetics of oxidation ofL-cystine by hexacyanoferrate(III) was studied in alkaline medium at 30 °C. The reaction was followed spectrophotometrically at λmax = 420 nm. The reaction was found to be first order dependence each on [HCF(III)] and [cystine]. It was found that the rate of the reaction increases with increase in [OH-]. The oxidation product of the reaction was found to be cysteic acid. A plausible mechanism has been proposed to account for the experimental results.

Oxidation Behaviors of DO3 Type Fe3Si Based Intermetallics at 900°C

2010 ◽  
Vol 146-147 ◽  
pp. 1904-1910
Author(s):  
Qi Zhou ◽  
Jian Gang Jia ◽  
Hong Shun Zhao ◽  
Xin Min Zhang
Keyword(s):  
Oxidation Resistance ◽  
Oxidation Product ◽  
Oxidation Reaction ◽  
Protective Oxide ◽  
Kinetics Of Oxidation ◽  
Good Oxidation Resistance ◽  
Arc Melting ◽  
Protective Oxide Film ◽  
Kinetics Of ◽  
Oxidation Behaviors

In the present work, intermetallics Fe3Si and Fe3 (Si1-xAlx) (x=0.33, 0.67, 0.80) produced by arc melting, were evaluated regarding the oxidation at 900°C in air. The test preformed was the isothermal and cyclic oxidation. The microstructures of oxide films were analyzed by XRD, SEM, EDS, EPMA. The result showed that the four kinds of intermetallics had good oxidation resistance at 900°C.The addition of Al element can increase the oxidation resistance of Fe3Si based intermetallics. The oxidation kinetics of the four intermetallics follows the rule of the parabola. The main oxidation product of Fe3Si is SiO2.The kinetics of oxidation reaction is mainly controlled by Si diffusion. The oxidation product of three Al alloying Fe3Si based intermetallics is Al oxide. Al moves outward from the substrate to form a protective oxide film which restrained the diffusion of Si and Fe outward.

Spectrocoulometry – a new spectro-electrochemical technique

1987 ◽  
Vol 52 (6) ◽  
pp. 1386-1396 ◽  
Author(s):  
Ján Mocák ◽  
Michal Németh ◽  
Mieczyslaw Lapkowski ◽  
Jerzy W. Strojek
Keyword(s):  
Optical Probe ◽  
Optical Signal ◽  
Open Circuit ◽  
Electrochemical Technique ◽  
Kinetics Of Oxidation ◽  
Hydrolytic Reaction ◽  
Experimental Errors ◽  
Mechanism And Kinetics ◽  
Kinetics Of

A spectrocoulometric macrocell with a direct-view optical probe was designed and constructed, where the optical signal is transferred by light-conducting glass or quartz fibres permitting to work at wavelengths above 410 or 300 nm. The method of measurement on the proposed equipment is described; it was tested in the study of the mechanism and kinetics of oxidation of Fe(bipy)32+ ions (bipy = 2,2'-bipyridyl) with the use of potentiostatic coulometric electrolysis with open-circuit relaxation at a suitable time. The primary product of electrolysis, Fe(bipy)33+, undergoes a follow-up hydrolytic reaction with the formation of a binuclear complex. The rate constant of the reaction of the first order involves the contributions, kBi, from all bases present in solution; the corresponding values for H2O, OH-, bipy, and CH3COO- ions at a ionic strength 0·5 mol dm-3 and 25 °C were determined as kOH = (5·0 ± 0·6) . 105 mol-1 dm3 s-1, kbipy = (1·3 ± 0·2) . 10-1 mol-1 dm3 s-1, kAc = (5·8 ± 1·0) . 10-2 mol-1 dm3 s-1, and kH2O is not significant with respect to experimental errors.

Effects of salts on the kinetics of oxidation of alkenes by thallic salts in aqueous solutions

1981 ◽  
Vol 46 (3) ◽  
pp. 693-700 ◽  
Author(s):  
Milan Strašák ◽  
Jaroslav Majer
Keyword(s):  
Aqueous Solutions ◽  
Phase Transfer ◽  
Heterogeneous Reaction ◽  
Qualitative Model ◽  
Kinetic Effect ◽  
Tetraalkylammonium Salts ◽  
Reaction Conditions ◽  
Kinetics Of Oxidation ◽  
Kinetics Of ◽  
Heterogeneous Reaction Conditions

The kinetics of oxidation of alkenes by thallic sulphate in aqueous solutions, involving the two reaction steps-the hydroxythallation and the dethallation - was studied, and the effect of salts on the kinetics was examined; this made it possible to specify more precisely the reaction mechanism and to suggest a qualitative model of the reaction coordinate. It was found that in homogeneous as well as in heterogeneous reaction conditions, the reaction can be accelerated appreciably by adding tetraalkylammonium salts. These salts not only operate as catalysts of the phase transfer, but also exert a significant kinetic effect, which can be explained with a simplification in terms of a stabilization of the transition state of the reaction.

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