Recovery of 2,6-dialkyl-naphthalene isomers

In a process for selective crystallization of 2,6-dialkyl-naphthalene selected from the group consisting of methyl-n-propyl-naphthalene, methyl isopropyl-naphthalene, ethyl-isopropyl-napthalene, ethyl-n-butyl-naphthalene, di-n-propyl-naphthalene, diisopropyl-naphthalene, methyl-amyl-naphthalene, eth...

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Bibliographische Detailangaben
Hauptverfasser:	ZELLERHOFF, ROBERT, STAEGLICH, PETER, OBERKOBUSCH, RUDOLF, HOELTMANN, WILHELM, CHARPEY, BERNHARD
Format:	Patent
Sprache:	eng
Schlagworte:	ACYCLIC OR CARBOCYCLIC COMPOUNDS CHEMISTRY GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS METALLURGY ORGANIC CHEMISTRY TECHNICAL SUBJECTS COVERED BY FORMER USPC TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ARTCOLLECTIONS [XRACs] AND DIGESTS
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Beschreibung
Zusammenfassung:	In a process for selective crystallization of 2,6-dialkyl-naphthalene selected from the group consisting of methyl-n-propyl-naphthalene, methyl isopropyl-naphthalene, ethyl-isopropyl-napthalene, ethyl-n-butyl-naphthalene, di-n-propyl-naphthalene, diisopropyl-naphthalene, methyl-amyl-naphthalene, ethyl-amyl-naphthalene, propyl-amyl-naphthalene, di-n-butyl-naphthalene and diisobutyl-naphthalene from their isomer mixtures from a polar solvent solution, the improvement comprising effecting the crystallization with constant stirring at a temperature from 25 DEG to -30 DEG C. to obtain the 2,6-dialkyl-naphthalene at least 95% pure.