Volatile Compounds in Acacia, Chestnut, Cherry, Ash, and Oak Woods, with a View to Their Use in Cooperage

Abstract

Extracts of wood from acacia, European ash, American ash, chestnut, cherry, and three oak species (Quercus pyrenaica, Quercus alba and Quercus petraea) before and after toasting in cooperage were studied by GC-MS. 110 compounds were detected, and 97 of them were identified. In general, all studied woods showed more lignin derivatives than lipid and carbohydrate derivatives, with a higher variety of compounds detected and abundance of them. The toasting led to an increase in the concentrations of most of these compounds, and this increase is especially important in acacia, chestnut and ash woods. The cis and trans isomers of beta-methyl-gamma-octalactone and isobutyrovanillone were only detected in oak wood, 3,4-dimethoxyphenol and 2,4-dihydroxybenzaldehyde only in acacia wood, and p-anisaldehyde and benzylsalicylate only in cherry wood, before and after toasting, and these compounds could be considered chemical markers for each one of these woods. Moreover, each wood has a characteristic volatile composition, from a quantitative point of view, and therefore we can expect a characteristic sensorial profile. The oak wood turned out to be the most balanced, since although it provides a lot of volatile compounds to the aroma and flavor of aged wine, it can do so without masking their primary and secondary aroma. On the whole, toasted acacia and chestnut woods showed a very high richness of studied compounds, as lignin as lipid and carbohydrate derivatives, while cherry and ash were much richer than toasted oak wood in lignin derivatives, but much poorer in lipid and carbohydrate derivatives.