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Glycerol as alternative co-solvent for water extraction of polyphenols from Carménère pomace: Hot pressurized liquid extraction and computational chemistry calculations

  • Nils Leander Huamán-Castilla
    ,
  • María Salomé Mariotti-Celis(corresponding author)
    ,
  • Maximiliano Martínez-Cifuentes
    ,
  • José Ricardo Pérez-Correa
*Corresponding author for this work
  • Universidad Nacional de Moquegua
    ,
  • Pontificia Universidad Católica de Chile
    ,
  • Universidad Tecnológica Metropolitana
    ,
  • Universidad Bernardo O'Higgins
Research Output:
Contribution to journal
Article
Peer-review

Open access

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Article number

474

Journal (Volume, Issue Number)

Biomolecules (Volume 10, Issue 3)

Publication milestones

  • Published - 01/03/2020

Publication status

Published - 01/03/2020

Publication IDs

  • Scopus: 85082808375
  • PubMed: 32244874

Abstract

Glycerol is a co-solvent for water extraction that has been shown to be highly effective for obtaining polyphenol extracts under atmospheric conditions. However, its efficacy under subcritical conditions has not yet been studied. We assessed different water-glycerol mixtures (15%, 32.5%, and 50%) in a hot pressurized liquid extraction system (HPLE: 10 MPa) at 90C, 120C, and 150C to obtain extracts of low molecular weight polyphenols from Carménère grape pomace. Under the same extraction conditions, glycerol as a co-solvent achieved significantly higher yields in polyphenols than ethanol. Optimal extraction conditions were 150C, with 32.5% glycerol for flavonols and 50% for flavanols, stilbenes, and phenolic acids. Considering gallic acid as a model molecule, computational chemistry calculations were applied to explain some unusual extraction outcomes. Furthermore, glycerol, methanol, ethanol, and ethylene glycol were studied to establish an incipient structure–property relationship. The high extraction yields of gallic acid obtained with water and glycerol solvent mixtures can be explained not only by the additional hydrogen bonds between glycerol and gallic acid as compared with the other alcohols, but also because the third hydroxyl group allows the formation of a three-centered hydrogen bond, which intensifies the strongest glycerol and gallic acid hydrogen bond. The above occurs both in neutral and deprotonated gallic acid. Consequently, glycerol confers to the extraction solvent a higher solvation energy of polyphenols than ethanol.