3 years ago

Enhancement in Conversion and Selectivity of Trivalerin Using Reactive Distillation

Enhancement in Conversion and Selectivity of Trivalerin Using Reactive Distillation
Kamalpreet Kaur, Amrit Pal Toor, Ravinder Kumar Wanchoo
The feasibility and potential of reactive distillation was studied to evaluate the enhancement in trivalerin selectivity in the esterification of valeric acid with glycerol, using n-octane as an entrainer over sulfated iron oxide catalyst. Effect of process parameters such as entrainer loading, reaction temperature, and reaction time was evaluated. Results have indicated that the selectivity toward trivalerin can be enhanced up to 95.07%, in comparison to batch process (74.80%), using the stoichiometric molar ratio, which describes the novelty of this work. Kinetic models such as pseudo-homogeneous, Eley–Rideal, and Langmuir–Hinshelwood model were used to study the kinetics of the reaction. The Eley–Rideal model supported the proposed mechanism with higher reliability and accuracy, resulting in an activation energy of 23.77 kJ/mol, which is plausibly less, compared to the batch process (27.37 kJ/mol).

Publisher URL: http://dx.doi.org/10.1021/acs.iecr.7b02098

DOI: 10.1021/acs.iecr.7b02098

You might also like
Never Miss Important Research

Researcher is an app designed by academics, for academics. Create a personalised feed in two minutes.
Choose from over 15,000 academics journals covering ten research areas then let Researcher deliver you papers tailored to your interests each day.

  • Download from Google Play
  • Download from App Store
  • Download from AppInChina

Researcher displays publicly available abstracts and doesn’t host any full article content. If the content is open access, we will direct clicks from the abstracts to the publisher website and display the PDF copy on our platform. Clicks to view the full text will be directed to the publisher website, where only users with subscriptions or access through their institution are able to view the full article.