Kinetics of 2-Methylfuran Acylation with Fatty Acid Anhydrides for Biorenewable Surfactants

Ankita V Naik, Kristeen E. Joseph, Manish M Shetty, M. Alexander Ardagh, Paul J. Dauenhauer

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

Friedel-Crafts acylation using long-chain fatty acid derivatives and biomass-derived furans is the key reaction to produce "alkyl furan ketones", an important precursor for biorenewable oleo-furan surfactants. In this work, the steady-state acylation kinetics and reaction mechanism were investigated using a model system of 2-methylfuran and n-octanoic anhydride in a fixed-bed tubular reactor using Al-MCM-41, a mesoporous aluminosilicate. An apparent activation energy (15.5 ± 1.4 kcal mol-1) was obtained for the formation of the acylated product, 2-octanoyl-5-methylfuran (2O5MF), for a temperature range of 348-408 K. The apparent reaction rate orders were â0.6 and â0.5 in the 2-methylfuran and anhydride concentrations, respectively, while near-zero apparent rate orders were measured in the product concentrations, indicating negligible product inhibition. An Eley-Rideal catalytic acylation mechanism was proposed to explain the experimentally observed apparent rate orders.

Original languageEnglish (US)
Pages (from-to)18616-18625
Number of pages10
JournalACS Sustainable Chemistry and Engineering
Volume8
Issue number50
DOIs
StatePublished - Dec 21 2020

Bibliographical note

Publisher Copyright:
© 2020 American Chemical Society.

Keywords

  • Al-MCM-41
  • acylation
  • biomass
  • chemical kinetics
  • oleo-furan surfactants
  • reaction mechanism

Fingerprint

Dive into the research topics of 'Kinetics of 2-Methylfuran Acylation with Fatty Acid Anhydrides for Biorenewable Surfactants'. Together they form a unique fingerprint.

Cite this