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R. Alberty, T. Bloomstein (1985)
Standard Chemical Thermodynamic Properties of Alkylnaphthalene Isomer GroupsJournal of Physical and Chemical Reference Data, 14
S. Pu, T. Inui (1996)
Synthesis of 2,6-dimethylnaphthalene by methylation of methylnaphthalene on various medium and large-pore zeolite catalystsApplied Catalysis A-general, 146
R. Gläser, Ruifeng Li, M. Hunger, S. Ernst, J. Weitkamp (1998)
Zeolite HNU-87: synthesis, characterization and catalytic properties in the shape-selective conversion of methylnaphthalenesCatalysis Letters, 50
H. Curran, Christine Wu, N. Marinov, W. Pitz, C. Westbrook, A. Burcat (2000)
The Ideal Gas Thermodynamics of Diesel Fuel Ingredients. I. Naphthalene Derivatives and Their RadicalsJournal of Physical and Chemical Reference Data, 29
R. Alberty, Michael Chung, A. Reif (1989)
Standard Chemical Thermodynamic Properties of Polycyclic Aromatic Hydrocarbons and Their Isomer Groups. II. Pyrene Series, Naphthopyrene Series, and Coronene SeriesJournal of Physical and Chemical Reference Data, 18
ISSN 1068-364X, Coke and Chemistry, 2007, Vol. 50, No. 10, pp. 304–309. © Allerton Press, Inc., 2007. Original Russian Text © A.A. Ozerenko, A.M. Gyul’maliev, S.G. Gagarin, 2007, published in Koks i Khimiya, 2007, No. 10, pp. 32–38. CHEMISTRY Physicochemical Properties and Thermodynamic Parameters of Methyl-Substituted Naphthalene Derivatives A. A. Ozerenko, A. M. Gyul’maliev, and S. G. Gagarin OOO Uglerodtopkhim Tekhnologiya DOI: 10.3103/S1068364X07100067 –1 –1 Recently, among the naphthalene derivatives in coal ± 4 kJ mol K in the specific heat and entropy, tar, interest has focused on 2,6-dimethylnaphthalene, according to [4]. Consequently, in the present work, we which is used for the production of polyester plastics. adopt a different additive approach, based on the spe- The small content of this derivative in coal tar precludes cific structure of methylnaphthalenes. The atoms in the its extraction, but its catalytic synthesis may be orga- initial naphthalene core are numbered as follows: nized on an industrial scale on the basis of coke-indus- 8 1 try naphthalene and its monomethyl derivatives [1]. 7 2 The development of this process calls for information 6 3 on the physicochemical properties of methylnaphtha- 5 4 lenes. Given the lack of experimental data, they must be
Coke and Chemistry – Springer Journals
Published: Feb 1, 2007
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