Proposed Models for Subcritical Water Extraction of Essential Oils

M. Khajenoori; A. Haghighi Asl; F. Hormozi

doi:10.1016/S1004-9541(08)60217-7

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Proposed Models for Subcritical Water Extraction of Essential Oils

Updated：2026-01-06

- Proposed Models for Subcritical Water Extraction of Essential Oils
- Proposed Models for Subcritical Water Extraction of Essential Oils
- 中国化学工程学报（英文版） 2009年17卷第3期页码：359-365
- Affiliations：
  
  Chemical Engineering Department, Faculty of Engineering, Semnan University, P. O. Box:35195-363, Semnan,Iran
- Author bio：
- Funds：
- DOI：10.1016/S1004-9541(08)60217-7
  中图分类号：
- 纸质出版：2009
- Accepted：
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M. Khajenoori, A. Haghighi Asl, F. Hormozi. Proposed Models for Subcritical Water Extraction of Essential Oils[J]. 中国化学工程学报（英文版）, 2009,17(3):359-365.

M. Khajenoori, A. Haghighi Asl, F. Hormozi. Proposed Models for Subcritical Water Extraction of Essential Oils[J]. , 2009, 17(3): 359-365.
M. Khajenoori, A. Haghighi Asl, F. Hormozi. Proposed Models for Subcritical Water Extraction of Essential Oils[J]. 中国化学工程学报（英文版）, 2009,17(3):359-365. DOI： 10.1016/S1004-9541(08)60217-7.

M. Khajenoori, A. Haghighi Asl, F. Hormozi. Proposed Models for Subcritical Water Extraction of Essential Oils[J]. , 2009, 17(3): 359-365. DOI： 10.1016/S1004-9541(08)60217-7.

摘要

Abstract

Mechanisms that control the extraction rate of essential oil from

Zataria multiflora

Boiss. (

Z. multiflora

) with subcritical water (SW) were studied. The extraction curves at different solvent flow rates were used to determine whether the extractions were limited primarily by the near equilibrium partitioning of the analyte between the matrix and solvent (

i.e

. partitioning thermodynamics) or by the rates of analyte desorption from the matrix (

i.e

. kinetics). Four simple models have been applied to describe the extraction profiles obtained with SW:(1) a model based solely on the thermodynamic distribution coefficient

which assumes that analyte desorption from the matrix is rapid compared to elution;(2) one-site kinetic model

which assumes that the extraction rate is limited by the analyte desorption rate from the matrix

and is not limited by the thermodynamic (

) partitioning that occurs during elution;(3) two-site kinetic model and (4) external mass transfer resistance model. For SW extraction

the thermodynamic elution of analytes from the matrix was the prevailing mechanism as evidenced by the fact that extraction rates increased proportionally with the SW flow rate. This was also confirmed by the fact that simple removal calculations based on determined

(for major essential oil compounds) gave good fits to experimental data for flow rates from 1 to 4 ml·min

-1

. The results suggested that the overall extraction me

chanism was influenced by solute partitioning equilibrium with external mass transfer through liquid film.

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