Catalytic synthesis of dialkyl sulfides from dialkyl disulfides
- Авторы: Mashkina A.V.1, Khairulina L.N.1
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Учреждения:
- Boreskov Institute of Catalysis, Siberian Branch
- Выпуск: Том 58, № 4 (2017)
- Страницы: 402-408
- Раздел: Article
- URL: https://journal-vniispk.ru/0023-1584/article/view/163113
- DOI: https://doi.org/10.1134/S0023158417040115
- ID: 163113
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Аннотация
Dialkyl disulfides R2S2 where R = Me, Et, or Pr, both as individual compounds and as their mixtures, isolated from petroleum products can turn into alkanethiols and dialkyl sulfides under the action of catalysts having strong acid sites and medium-strength basic sites on their surface. In a helium atmosphere, the main conversion products are alkanethiols, while dialkyl sulfides form in low yield at a selectivity of no higher than 20%. A much higher dialkyl sulfide selectivity is attained in the reaction involving methanol. The most efficient catalyst for this reaction is alumina, with which the dialkyl sulfide selectivity is up to 99%.
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Об авторах
A. Mashkina
Boreskov Institute of Catalysis, Siberian Branch
Автор, ответственный за переписку.
Email: amash@catalysis.ru
Россия, Novosibirsk, 630090
L. Khairulina
Boreskov Institute of Catalysis, Siberian Branch
Email: amash@catalysis.ru
Россия, Novosibirsk, 630090
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