脱氢
蒽
萘
十氢萘
化学
苯
菲
催化作用
联苯
环己烷
光化学
环烷烃
空间速度
冷凝
有机化学
热力学
物理
选择性
作者
А. Н. Каленчук,В. И. Богдан,С. Ф. Дунаев,Л. М. Кустов
出处
期刊:Fuel
[Elsevier BV]
日期:2020-07-14
卷期号:280: 118625-118625
被引量:51
标识
DOI:10.1016/j.fuel.2020.118625
摘要
Abstract The reversible reactions of hydrogenation-dehydrogenation of polycyclic aromatic hydrocarbons with a different extent of condensation (naphthalene, anthracene, biphenyl, meta- and para-terphenyl isomers) were studied in comparison with benzene on a 3%Pt/C catalyst. Hydrogenation of naphthalene and anthracene was carried out at T = 280 °C, P = 90 atm, whereas the reaction of benzene, biphenyl and terphenyl isomers was performed at T = 180 °C, P = 70 atm in an autoclave. Dehydrogenation of the corresponding polycyclic naphthenes (cyclohexane, decalin, perhydroanthracene, bicyclohexyl, ortho, meta, and para-isomers of perhydroterphenyl) was carried out in the temperature range of 280 to 340 °C in a flow setup at the volume hourly space velocity of 1 h−1 and atmospheric pressure. Correlation dependences of the reaction rates of hydrogenation-dehydrogenation of the studied substrates on their structure and extent of condensation were found.
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