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Low‐temperature, solvent‐free dehydration of cineoles with heterogeneous acid catalysts for the production of high‐density biofuels
Author(s) -
Meylemans Heather A.,
Quintana Roxanne L.,
Rex Megan L.,
Harvey Benjamin G.
Publication year - 2014
Publication title -
journal of chemical technology and biotechnology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.64
H-Index - 117
eISSN - 1097-4660
pISSN - 0268-2575
DOI - 10.1002/jctb.4390
Subject(s) - dehydration , biofuel , catalysis , chemistry , solvent , organic chemistry , chemical engineering , biochemistry , waste management , engineering
BACKGROUND Oxygenated terpenoids such as 1,4‐cineole and 1,8‐cineole can be major components of turpentine and essential oils. These terpenoids can also be produced from sugars via a biosynthetic approach. Catalytic deoxygenation of these substrates has the potential to efficiently generate commercially important chemicals and high density fuels for turbine or diesel propulsion.RESULTS The low‐temperature deoxygenation reactions of 1,4‐cineole and 1,8‐cineole over the heterogeneous acid catalysts Amberlyst‐15, Nafion SAC ‐13, and Montmorillonite K10 have been studied. 1,4‐cineole was found to isomerize to terpinene‐1‐ol followed by dehydration to a mixture primarily composed of α‐ and γ‐terpinene. In a similar manner, 1,8‐cineole was found to isomerize to α‐terpineol followed by dehydration to primarily terpinolene and α‐terpinene. Amberlyst‐15 was the most active catalyst on a mass basis and gave 100% conversion of 1,4‐cineole in 24 h at 85°C. Longer reaction times or higher reaction temperatures led to significant conversion of the dehydrated monoterpenes to diterpenes. Similar trends were observed for Nafion SAC ‐13 and Montmorillonite K10 .CONCLUSION This work provides important mechanistic information regarding the dehydration chemistry of cineoles and shows the potential of heterogeneous acid catalysts to effectively convert oxygenated terpenoids to high density hydrocarbon mixtures with potential uses as renewable diesel fuels. Published 2014. This article is a U.S. Government work and is in the public domain in the USA.