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Experimental and theoretical study of the thermal decomposition of ethyl acetate during fast pyrolysis

Authors
  • Vargas Solis, Diana Cristina
  • Salazar, Sebastián
  • Mora, José R.
  • Van Geem, Kevin
  • Almeida Streitwieser, Daniela
Publication Date
Jan 01, 2020
Identifiers
DOI: 10.1016/j.cherd.2020.03.001
OAI: oai:archive.ugent.be:8656548
Source
Ghent University Institutional Archive
Keywords
Language
English
License
Green
External links

Abstract

The thermal decomposition of ethyl acetate was experimentally studied in a newly designed fast pyrolysis set-up. The results were compared to theoretical calculations and literature values in order to proof the experimental concept. The reaction was carried out in a free fall tubular reactor with a residence time of 0.15 s. The identification and quantification of products stream composition was performed online using a GC-TCD/FID. First, an overview of the reaction rate at feed volumes of 0.25, 0.50 and 0.75 mL was obtained at reaction temperature between 400 to 600 degrees C in intervals of 50 degrees C. As a result mass transfer limitation for feeds larger than 0.5 mL were identified. For the second approach, a constant feed volume of 0.25 mL and temperatures between 420 to 550 degrees C were investigated. Using the experimental results, a global kinetic model is proposed for the thermal decomposition of ethyl acetate into ethylene and acetic acid through a first order unimolecular reaction. Also, theoretical calculations were performed at wB97XD/6-311++G(d,p) level. A concerted mechanism through a six-membered transition state was identified in the reaction path. The theoretical and experimental activation energy values lie within the literature values between 193 and 213 kJ/mol. 2020 The Authors. Published by Elsevier B.V. on behalf of Institution of Chemical Engineers. This is an open access article under the CC BY-NC -ND license (http://creativecommons.orgilicenseseby-nc-nd/450/).

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