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Kinetic Study on Esterification of Acetic Acid with Isopropyl Alcohol Catalyzed by Ion Exchange Resin

[Image: see text] Esterification kinetics on acetic acid with isopropyl alcohol was studied in an intensified fixed bed reactor at 333–353 K with Amberlyst 36 Wet. The effects of volume flow rate, molar ratio of reactants, catalyst loading, and operating temperature were investigated and optimized....

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Autores principales: Liu, Ying, Liu, Jia, Yan, Hanzhao, Zhou, Zheng, Zhou, Aidong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868888/
https://www.ncbi.nlm.nih.gov/pubmed/31763570
http://dx.doi.org/10.1021/acsomega.9b02994
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author Liu, Ying
Liu, Jia
Yan, Hanzhao
Zhou, Zheng
Zhou, Aidong
author_facet Liu, Ying
Liu, Jia
Yan, Hanzhao
Zhou, Zheng
Zhou, Aidong
author_sort Liu, Ying
collection PubMed
description [Image: see text] Esterification kinetics on acetic acid with isopropyl alcohol was studied in an intensified fixed bed reactor at 333–353 K with Amberlyst 36 Wet. The effects of volume flow rate, molar ratio of reactants, catalyst loading, and operating temperature were investigated and optimized. The method of UNIFAC was applied to calculate the activity coefficient of each component for correcting the nonideality of the solution. Reaction enthalpy, entropy, and Gibbs free energy were calculated in different cases. The pseudohomogeneous model, Eley–Rideal model, and Langmuir–Hinshelwood–Hougen–Watson model were used to establish kinetic equations of the reaction conducted in the IFBR. It was proved that the LHHW model can accurately describe the esterification kinetics in the intensified fixed bed reactor.
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spelling pubmed-68688882019-11-22 Kinetic Study on Esterification of Acetic Acid with Isopropyl Alcohol Catalyzed by Ion Exchange Resin Liu, Ying Liu, Jia Yan, Hanzhao Zhou, Zheng Zhou, Aidong ACS Omega [Image: see text] Esterification kinetics on acetic acid with isopropyl alcohol was studied in an intensified fixed bed reactor at 333–353 K with Amberlyst 36 Wet. The effects of volume flow rate, molar ratio of reactants, catalyst loading, and operating temperature were investigated and optimized. The method of UNIFAC was applied to calculate the activity coefficient of each component for correcting the nonideality of the solution. Reaction enthalpy, entropy, and Gibbs free energy were calculated in different cases. The pseudohomogeneous model, Eley–Rideal model, and Langmuir–Hinshelwood–Hougen–Watson model were used to establish kinetic equations of the reaction conducted in the IFBR. It was proved that the LHHW model can accurately describe the esterification kinetics in the intensified fixed bed reactor. American Chemical Society 2019-11-07 /pmc/articles/PMC6868888/ /pubmed/31763570 http://dx.doi.org/10.1021/acsomega.9b02994 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Liu, Ying
Liu, Jia
Yan, Hanzhao
Zhou, Zheng
Zhou, Aidong
Kinetic Study on Esterification of Acetic Acid with Isopropyl Alcohol Catalyzed by Ion Exchange Resin
title Kinetic Study on Esterification of Acetic Acid with Isopropyl Alcohol Catalyzed by Ion Exchange Resin
title_full Kinetic Study on Esterification of Acetic Acid with Isopropyl Alcohol Catalyzed by Ion Exchange Resin
title_fullStr Kinetic Study on Esterification of Acetic Acid with Isopropyl Alcohol Catalyzed by Ion Exchange Resin
title_full_unstemmed Kinetic Study on Esterification of Acetic Acid with Isopropyl Alcohol Catalyzed by Ion Exchange Resin
title_short Kinetic Study on Esterification of Acetic Acid with Isopropyl Alcohol Catalyzed by Ion Exchange Resin
title_sort kinetic study on esterification of acetic acid with isopropyl alcohol catalyzed by ion exchange resin
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868888/
https://www.ncbi.nlm.nih.gov/pubmed/31763570
http://dx.doi.org/10.1021/acsomega.9b02994
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