Effect of the structure of the ortho, meta, and para isomers of perhydroterphenyl on their reactivity in heterogeneous catalytic dehydrogenation
- 作者: Kalenchuk A.N.1,2, Bogdan V.I.1,2, Bogorodskii S.E.3, Kustov L.M.1,2
-
隶属关系:
- Faculty of Chemistry
- Zelinsky Institute of Organic Chemistry
- Institute on Laser and Information Technologies
- 期: 卷 57, 编号 2 (2016)
- 页面: 219-223
- 栏目: Article
- URL: https://journal-vniispk.ru/0023-1584/article/view/162399
- DOI: https://doi.org/10.1134/S0023158416020038
- ID: 162399
如何引用文章
详细
The kinetics of the dehydrogenation of the individual ortho, meta, and para isomers of perhydroterphenyl and their mixtures over a (3 wt % Pt)/C catalyst has been investigated in a flow reactor at 280–340°C. The rate of the isomerization of the stereoisomers of the initial substrate (perhydroterphenyl) and terphenyl dehydrogenation products has an effect on the hydrogen release kinetics. The highest reactivity in isomerization is shown by the ortho isomer. The largest amount of hydrogen (7.0 wt %) is released in the dehy-drogenation of perhydro-meta-terphenyl and perhydro-para-terphenyl, whose conversion at 320°C is 96%.
作者简介
A. Kalenchuk
Faculty of Chemistry; Zelinsky Institute of Organic Chemistry
编辑信件的主要联系方式.
Email: akalenchuk@yandex.ru
俄罗斯联邦, Moscow, 119991; Moscow, 119991
V. Bogdan
Faculty of Chemistry; Zelinsky Institute of Organic Chemistry
Email: akalenchuk@yandex.ru
俄罗斯联邦, Moscow, 119991; Moscow, 119991
S. Bogorodskii
Institute on Laser and Information Technologies
Email: akalenchuk@yandex.ru
俄罗斯联邦, Troitsk, Moscow oblast, 142190
L. Kustov
Faculty of Chemistry; Zelinsky Institute of Organic Chemistry
Email: akalenchuk@yandex.ru
俄罗斯联邦, Moscow, 119991; Moscow, 119991
补充文件
