2007
DOI: 10.1016/j.jaap.2006.04.006
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Limonene ethers from tire pyrolysis oil

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Cited by 28 publications
(9 citation statements)
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“…12,13 Stanciulescu et al reported the superior activity of zeolite beta in the etherification of limonene extracted from tyre pyrolysis oil when compared to zeolites like ZSM-5, Y, X and ion exchange resin Amberlyst-15. 14,15 D-Limonene etherification was also reported by Catrinescu et al over acid and ion exchanged clays. 16 Herein we report the first demonstration of a heterogeneous catalytic process for chemoselective etherification of β-citronellene over zeolite beta to produce ethers useful as fragrances and flavor additives as well as developing a solvent for flexographic printing plates.…”
Section: Introductionsupporting
confidence: 56%
“…12,13 Stanciulescu et al reported the superior activity of zeolite beta in the etherification of limonene extracted from tyre pyrolysis oil when compared to zeolites like ZSM-5, Y, X and ion exchange resin Amberlyst-15. 14,15 D-Limonene etherification was also reported by Catrinescu et al over acid and ion exchanged clays. 16 Herein we report the first demonstration of a heterogeneous catalytic process for chemoselective etherification of β-citronellene over zeolite beta to produce ethers useful as fragrances and flavor additives as well as developing a solvent for flexographic printing plates.…”
Section: Introductionsupporting
confidence: 56%
“…Furthermore, the biological activity of limonene, such as its chemopreventive activity against rat mammary cancer, has been recently investigated [7]. In order to enhance the marketability of tire pyrolysis liquids, Stanciulescu and Ikura [14,15] separated limonene-enriched fraction using vacuum distillations and reacted with methanol to produce limonene ethers. Methyl limonene ether is a high value product and has a very pleasant fragrance.…”
Section: Introductionmentioning
confidence: 99%
“…Limonene is classified as a cyclic monoterpene [17] with the chemical formula C 10 H 16 and the IUPAC name 1-methyl-4-(1-methylethenyl)-cyclohexene. Its common name derives from lemons: limonene is present in the skins of these fruit and is responsible for their distinctive smell.…”
Section: Chemical Structure Of Limonenementioning
confidence: 99%