Purification of 2,6-Diisopropylnaphthalene by Static Melt Crystallization from a Mixture Containing Diisopropylnaphthalene Isomers

2,6-Diisopropylnaphthalene (2,6-DIPN), as the precursor of important monomer 2,6-naphthalene dicarboxylic acid, could be produced by the shape-selective isopropylation of naphthalene with propene resulting in an isomeric mixture having different alkylation levels. Since the boiling points of DIPNs w...

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Bibliographic Details
Published inChinese journal of chemistry Vol. 25; no. 1; pp. 108 - 112
Main Author 田正华 贾宏敏 赵桂利 胡伟琪
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 2007
WILEY‐VCH Verlag
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ISSN1001-604X
1614-7065
DOI10.1002/cjoc.200790002

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Summary:2,6-Diisopropylnaphthalene (2,6-DIPN), as the precursor of important monomer 2,6-naphthalene dicarboxylic acid, could be produced by the shape-selective isopropylation of naphthalene with propene resulting in an isomeric mixture having different alkylation levels. Since the boiling points of DIPNs were very close and the differences of melting points in-between isomers were quite distinctive, the static melt crystallization was applied to separate and purify 2,6-DIPN from its isomers. 2,6-DIPN with purity ≥99% was produced through a process of three stages: crystallization→sweating→melting. The phase diagram of 2,6-DIPN-2,7-DIPN binary system was plotted to opti- mize the temperature control of crystallization. By repeated crystallization of melts with different concentration levels, the yield of pure 2,6-DIPN could be enhanced to 87%. No solvent was necessary. Keywords 2,6-diisopropylnaphthalene, static melt crystallization, crystallization rate, sweating rate, eutectic temperature
Bibliography:31-1547/O6
2,6-diisopropylnaphthalene, static melt crystallization, crystallization rate, sweating rate, eutectic temperature
O625.151
ArticleID:CJOC200790002
ark:/67375/WNG-6SXCMCX5-1
istex:C205F93478A3BA1D25E393D9A236D91BC532485F
the Northeast Rejuvenation Strategy Foundation of Anshan city - No. 032042
ISSN:1001-604X
1614-7065
DOI:10.1002/cjoc.200790002