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- W2072665064 abstract "Gaseous 1-phenylnaphthalene was allowed to react with two H+ZSM-5 zeolites distinguished by a different acidity. The isomerisation to 2-phenyl naphthalene was the principal reaction observed, but also fragmentation to benzene plus naphthalene and self-condensation to fluoranthene occurred. The yields of all the products were higher when the more acidic zeolite was used. A temperature dependence study showed that, varying the temperature from 390 to 450°C, the yield of fluoranthene increased. By the Arrhenius plots for fluoranthene formation it was concluded that the activation energy of this reaction is independent on the acidity of zeolites." @default.
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- W2072665064 date "1990-01-01" @default.
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- W2072665064 title "An ionic pathway to fluoranthene" @default.
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- W2072665064 doi "https://doi.org/10.1016/0045-6535(90)90003-c" @default.
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