Potentiometric method for determination of kinetic characteristics of radical reactions in aqueous media


Дәйексөз келтіру

Толық мәтін

Ашық рұқсат Ашық рұқсат
Рұқсат жабық Рұқсат берілді
Рұқсат жабық Тек жазылушылар үшін

Аннотация

Kinetic features of the reactions of K4[Fe(CN)6] with radicals initiated by water-soluble azo-initiator 2,2′-azobis(2-amidinopropane) dihydrochloride (AAPH) at 37 °C were studied using the potentiometric method. Potassium ferrocyanide was shown to be a radical acceptor, whereas K3[Fe(CN)6] formed by the oxidation with the radicals in combination with K4[Fe(CN)6] is an electrochemical system, the study of which makes it possible to determine kinetic characteristics of radical reactions. The rate constants for the reactions of peroxide radicals RO2 · with K4[Fe(CN)6] were calculated.

Авторлар туралы

A. Ivanova

Ural Federal University named after the First President of Russia B. N. Yeltsin, Chemical Technological Institute

Хат алмасуға жауапты Автор.
Email: a.v.ivanova@urfu.ru
Ресей, 19 ul. Mira, Ekaterinburg, 620002

E. Gerasimova

Ural Federal University named after the First President of Russia B. N. Yeltsin, Chemical Technological Institute

Email: a.v.ivanova@urfu.ru
Ресей, 19 ul. Mira, Ekaterinburg, 620002

E. Gazizullina

Ural Federal University named after the First President of Russia B. N. Yeltsin, Chemical Technological Institute

Email: a.v.ivanova@urfu.ru
Ресей, 19 ul. Mira, Ekaterinburg, 620002

A. Davletchurina

Ural Federal University named after the First President of Russia B. N. Yeltsin, Chemical Technological Institute

Email: a.v.ivanova@urfu.ru
Ресей, 19 ul. Mira, Ekaterinburg, 620002

A. Kozitsina

Ural Federal University named after the First President of Russia B. N. Yeltsin, Chemical Technological Institute

Email: a.v.ivanova@urfu.ru
Ресей, 19 ul. Mira, Ekaterinburg, 620002

O. Kasaikina

N. N. Semenov Institute of Chemical Physics, Russian Academy of Sciences

Email: a.v.ivanova@urfu.ru
Ресей, 4 ul. Kosygina, Moscow, 119991


© Springer Science+Business Media, LLC, part of Springer Nature, 2017

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