Reply to the ‘Comment on “Theoretical investigations on hydrogen peroxide decomposition in aquo”’ by W. H. Koppenol, Phys. Chem. Chem. Phys., 2021, 23, DOI: 10.1039/D1CP03545B

Author(s):  
Takao Tsuneda ◽  
Tetsuya Taketsugu

The H2O2 decomposition reaction mechanism based on the production of a de facto Fe+ ion hydration complex is strongly supported by a simple test based on the Gibbs energies considering the O–O bond dissociation of H2O2.

2018 ◽  
Vol 20 (38) ◽  
pp. 24992-24999 ◽  
Author(s):  
Takao Tsuneda ◽  
Tetsuya Taketsugu

Hydrogen peroxide (H2O2) decomposition mechanisms in the absence and presence of iron ions in aqueous solution, which contain no OH radical formation, are theoretically determined. H2O2 decomposition in the presence of iron ions is driven by electron transfer to the iron ion and proceeds by hydrogen transfers in the hydrogen bond network around H2O2.


Author(s):  
Vladimir Sergeevich Dolmatov ◽  
Sergey Kuznetsov

Abstract Coatings of TaC and NbC and Mo2C crystals on carbon fibers were obtained by currentless transfer in molten salts. Investigation of electrocatalytic properties of these compositions in the reaction of the hydrogen peroxide decomposition was carried out. It was determined that the hydrogen peroxide decomposition reaction has a zero order for all refractory metal carbides. Using the values of the rate constants at different temperatures the activation energies for the reaction of the hydrogen peroxide decomposition on refractory metal carbides were calculated using the Arrhenius equation. It has been established that coating of NbC on carbon fibers has a higher electrocatalytical properties in comparison with other carbides. The electrocatalytic properties of NbC/C, TaC/C and Mo2C/C composites were studied also by cyclic voltammetry.


1980 ◽  
Vol 45 (6) ◽  
pp. 1780-1784 ◽  
Author(s):  
Atanas Andreev ◽  
Lachezar Prahov ◽  
Dimitar Shopov

The formation of Oxygen paramagnetic adducts of Co(II) containing ion-exchange resins in the presence of adsorbed ethylenediamine has been found. The EPR parameters of a complex of the type Co(III) (en)2O-2 and of O-2 species formed in the presence of Co(en)2+3 have been described. The catalytic properties of Co-ethylenediamine surface complexes with respect to the hydrogen peroxide decomposition reaction have been investigated and a probable mechanism has been suggested.


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