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2020, br. 40, str. 33-39
GC/MS chemical analysis of lavandin (Lavandula x intermedia) hydrolat: Successive extraction fractions
(naslov ne postoji na srpskom)
Institut za proučavanje lekovitog bilja 'Dr Josif Pančić', Beograd

Ministarstvo prosvete, nauke i tehnološkog razvoja Republike Srbije (institucija: Institut za proučavanje lekovitog bilja 'Dr Josif Pančić', Beograd) (MPNTR - 451-03-68/2020-14/200003)

(ne postoji na srpskom)
Hydrolats are valuable co-products of the essential oil distillation process, whose volatile compounds can be quantified by various methods. In this paper, we have tried to estimate the liquid-liquid extraction cycle number threshold for volatile compounds quantification of lavandin (Lavandula x intermedia) hydrolat. For this purpose, ten consecutive hydrolat extractions with n-hexane were analyzed GC/MS with hexadecane (C16) as an internal standard and compared with the lavandin essential oil. The chemical composition of the lavandin hydrolat showed similarity with its essential oil to the great extent, while volatile compounds dissolved in hydrolat exclusively belonged to the class of oxygenated monoterpenes. The total amount of extracted compounds has been estimated to 2174.2 mg/L, where the most dominant compounds in lavandin hydrolat were cisand trans-furanoid linalool oxide (676.3 and 634.1 mg/L, respectively), followed by much smaller amounts of linalool, camphor, and 1,8-cineole (167.6, 157.0, and 148.2 mg/L, respectively). Cumulative recoveries of total compounds yield after the third, fifth, and eighth extractions were 88 %, 96 %, and 99 %, respectively. Combined fraction analysis confirmed that in the first 5 cycles more than 95 % of the total yield (from 10 cycles) of extracted volatile compounds can be collected. Based on the results of this study, for volatile compounds quantification in lavandin hydrolat, 5 cycles of n-hexane liquid-liquid extraction can be recommended.
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O članku

jezik rada: engleski
vrsta rada: istraživanja
DOI: 10.5937/leksir2040033P
primljen: 10.09.2020.
prihvaćen: 18.11.2020.
objavljen onlajn: 19.12.2020.
objavljen: 25.12.2020.
objavljen u SCIndeksu: 31.12.2020.

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