Chain explosion in the oxidation of hydrogen for intense degrees of burn-up

1974 ◽  
Vol 10 (3) ◽  
pp. 325-328
Author(s):  
V. I. Babushok ◽  
V. A. Bunev ◽  
V. S. Babkin ◽  
L. A. Lovachev

1984 ◽  
Vol 49 (10) ◽  
pp. 2320-2331 ◽  
Author(s):  
Miroslav Březina ◽  
Martin Wedell

Reduction of oxygen and oxidation of hydrogen peroxide at the dropping mercury electrode are electrochemical processes strongly influenced both by the pH value and the anions in solution. With decreasing pH, both processes become irreversible, especially in the presence of anions with a negative φ2 potential of the diffusion part of the double layer. In the case of irreversible oxygen reduction, the concept that the rate-controlling step of the electrode process is the acceptance of the first electron with the formation of the superoxide anion, O2-, was substantiated. Oxidation of hydrogen peroxide becomes irreversible at a lower pH value than the reduction of oxygen. The slowest, i.e. rate-controlling step of the electrode process in borate buffers at pH 9-10 is the transfer of the second electron, i.e. oxidation of superoxide to oxygen.



2019 ◽  
Vol 191 ◽  
pp. 121-128 ◽  
Author(s):  
Minghui Sun ◽  
Xuzhen Wang ◽  
Xin Pan ◽  
Lang Liu ◽  
Yong Li ◽  
...  


2005 ◽  
Vol 41 (5) ◽  
pp. 318-322
Author(s):  
V. K. Yatsimirskii ◽  
N. P. Maksimovich ◽  
O. Yu. Boldyreva ◽  
N. V. Nikitina ◽  
A. G. Telegeeva




2009 ◽  
Vol 610-613 ◽  
pp. 161-164
Author(s):  
Li Li Liang ◽  
Xue Gang Luo ◽  
Xiao Yan Lin

A ferric stearate electrode was made by doctor-blade methods using the Fluorine tin oxide (FTO) conductive glass. The electrochemical behavior of ferric stearate electrode was studied by the cyclic voltammetry. The electro-catalytic effects of ferric stearate on H2O2 were also investigated by cyclic voltammetry.



2005 ◽  
Vol 4 (2) ◽  
pp. 157-175 ◽  
Author(s):  
Guoxiong Hua ◽  
Qingzhi Zhang ◽  
Derek McManus ◽  
Alex M. Z. Slawin ◽  
J. Derek Woollins


Author(s):  
Eduard G. Karpov ◽  
Ievgen I. Nedrygailov

We report on the unusual properties of single-faced SiC metal-semiconductor heterojunction nanostructures manifested by the ability to atalyze the hydrogen oxidation reaction, and also maintain internal electron emission over the Schottky barriers. As a result a stationary current has been detected in the preheated nanostructure when exposed to the oxyhydrogen gas mixture flux. The structures maintain both the non-adiabatic and electron-phonon channels of energy transfer, and the results of studies indicate the possibility for a very efficient conversion of chemical energy released in the catalytic oxidation of hydrogen into electricity.



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