Radiation-Chemical Transformations of Ethylene Glycol and Its Deuterated Derivative in Deaerated Aqueous Solutions

Мұқаба

Дәйексөз келтіру

Толық мәтін

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

Аннотация

This study is devoted to the effect of complete deuteration of the ethylene glycol carbon skeleton on the formation of its radiation-induced free-radical transformations products in deaerated aqueous solutions at pH 7.00 ± 0.10 and a dose rate of 0.064 ± 0.002 Gy/s. It has been established that the chain process of fragmentation of carbon-centered ethylene glycol radicals (∙CH(OH)CH2OH) plays an important role in the formation of acetaldehyde. The replacement of protium atoms located at carbon atoms by deuterium decreased the radiation-chemical yield of acetaldehyde in aqueous 1 M solutions of diols by a factor of 8. The results of this study indicate that the use of deuterium exchange at the carbon skeleton of organic molecules is a promising way for increasing their resistance to radiation-induced free radical fragmentation processes.

Авторлар туралы

O. Urbanovich

Belarusian State University

Email: olga.urbanovich@gmail.com
Minsk, 220030 Belarus

A. Davydenko

Belarusian State University

Email: olga.urbanovich@gmail.com
Minsk, 220030 Belarus

R. Sverdlov

Belarusian State University; Research Institute for Physicochemical Problems, Belarusian State Universit

Email: olga.urbanovich@gmail.com
Minsk, 220030 Belarus; Minsk, 220006 Belarus

A. Bekish

Institute of Physical and Organic Chemistry, National Academy of Sciences of Belarus

Email: olga.urbanovich@gmail.com
Minsk, 220072 Belarus

S. Lastovskii

Scientific and Practical Center for Materials Science, National Academy of Sciences of Belarus

Email: olga.urbanovich@gmail.com
Minsk, 220072 Belarus

E. Tochilin

Scientific and Practical Center for Materials Science, National Academy of Sciences of Belarus

Хат алмасуға жауапты Автор.
Email: olga.urbanovich@gmail.com
Minsk, 220072 Belarus

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© О.В. Урбанович, А.И. Давыденко, Р.Л. Свердлов, А.В. Бекиш, С.Б. Ластовский, Е.В. Точилин, 2023