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  4. Vanadate ion-catalyzed oxidation of methane with hydrogen peroxide in an aqueous solution
 
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Vanadate ion-catalyzed oxidation of methane with hydrogen peroxide in an aqueous solution

Auteur(s)
Romakh, Vladimir B
Süss-Fink, Georg 
Institut de chimie 
Shul'pin, Georgiy B
Date de parution
2008
In
Petroleum Chemistry
Vol.
6
No
48
De la page
440
A la page
443
Mots-clés
  • O-2-H2O2-VANADIUM DERIVATIVE-PYRAZINE-2-CARBOXYLIC ACID
  • H2O2-VANADIUM
  • COMPLEX-PYRAZINE-2-CARBOXYLIC ACID
  • PYRAZINE-2-CARBOXYLIC ACID
  • VANADIUM COMPLEXES
  • ALKYL PEROXIDES
  • LOWER ALKANES
  • REAGENT
  • MECHANISM
  • FUNCTIONALIZATION
  • ACETONITRILE
  • O-2-H2O2-VANADIUM DER...

  • H2O2-VANADIUM

  • COMPLEX-PYRAZINE-2-CA...

  • PYRAZINE-2-CARBOXYLIC...

  • VANADIUM COMPLEXES

  • ALKYL PEROXIDES

  • LOWER ALKANES

  • REAGENT

  • MECHANISM

  • FUNCTIONALIZATION

  • ACETONITRILE

Résumé
It was shown that, unlike methane oxidation with the reagent "hydrogen peroxide-vanadate anion-pyrazine-2-carboxylic acid (PCA)" in acetonitrile, the performance of the process in an aqueous solution is accompanied by the intense parallel degradation of the cocatalyst. Therefore, relatively high yields of methane oxidation products (largely, formic acid) cannot be attained unless a rather high PCA concentration is used. Admixtures of a strong acid (sulfuric, trifluoroacetic, or perchloric) increase the yield of the products. It was found that perchloric acid can also be used as a cocatalyst instead of PCA.
Identifiants
https://libra.unine.ch/handle/123456789/13408
Type de publication
journal article
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