Conclusions
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1.
The conversions of n-octane, 1-methyl-2-ethyl-cyclopentane, n-propylcyclopentane, ethylbenzene, p-, m-, and o-xylenes in the presence of a catalyst 0.6% Pt/γ-Al2O3 at atmospheric pressure in a stream of hydrogen were investigated in the temperature interval 300–520°, using a microreactor.
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2.
The aromatization of n-octane is accompanied by the reaction of C6-dehydrocyclization, forming 1-methyl-2-ethylcyclopentane and n-propylcyclopentane.
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3.
Alkylcyclopentanes undergo dehydroisomerization under the selected experimental conditions, forming aromatic hydrocarbons, hydrogenolysis, and to a negligible degree dehydrogenation, forming alkylcyclopentenes.
-
4.
Ethylbenzene and all three xylenes do not isomerize into one another, but undergo dealkylation, forming benzene and toluene.
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The article is published on the basis of a resolution of the Conference of Editors-in-Chief of the Journals of the Academy of Sciences of the USSR from July 12, 1962, as the dissertation work of V. G. Vlasov.
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No.1, pp. 64–69, January, 1970.
The authors would like to thank I. V. Gostunskaya for her discussion of a number of problems.
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Vlasov, V.G., Fomichev, Y.V. & Kazanskii, B.A. Aromatization of n-octane in the presence of an aluminoplatinum catalyst. Russ Chem Bull 19, 59–64 (1970). https://doi.org/10.1007/BF00913924
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DOI: https://doi.org/10.1007/BF00913924