Obtaining glycerol carbonate and glycols using thermomorphic systems based on glycerol and cyclic organic carbonates: Kinetic studies

J. Esteban, A.J. Vorholt

Research output: Contribution to journalArticlepeer-review

Abstract

Glycerol carbonate has mostly been synthesized by transesterification of glycerol with dimethyl carbonate and ethylene carbonate. We propose to obtain it using propylene and butylene carbonate as co-substrates with Na2CO3 as catalyst, also generating 1,2-propanediol and 1,2-butanediol. The reactants exhibit thermomorphic behavior, so we capitalized on this feature to avoid mass transfer limitations instead of using co-solvents. The kinetics of both reactions were studied, obtaining activation energies and deactivation constants of 67.13 ± 1.82 kJ mol−1 and 0.14 ± 0.02 min−1 for the reaction between glycerol and propylene carbonate and 58.56 ± 1.10 kJ mol−1 and 0.39 ± 0.03 min−1 for the reaction of glycerol with butylene carbonate. © 2018 The Korean Society of Industrial and Engineering Chemistry
Original languageEnglish
Pages (from-to)124-132
Number of pages9
JournalJournal of Industrial and Engineering Chemistry
Volume63
Early online date12 Feb 2018
DOIs
Publication statusPublished - 2018

Keywords

  • Glycerol
  • Glycerol carbonate
  • Kinetic model
  • Solventless reaction
  • Thermomorphic system
  • Activation energy
  • Butenes
  • Carbonation
  • Ethylene
  • Kinetic theory
  • Kinetics
  • Mass transfer
  • Propylene
  • Reaction kinetics
  • Sodium compounds
  • Solid state reactions
  • Deactivation constants
  • Kinetic modeling
  • Mass transfer limitation
  • Propylene carbonate
  • Solventless reactions
  • Thermomorphic behavior

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