Optimization of process variables for esterification of bio-oil model compounds by a heteropolyacid catalyst

In this work, the catalytic upgrading of a bio-oil model compound via esterification with ethanol was studied using 12-tungstosilicic acid as the catalyst. The response surface method was used to investigate and optimize the process variables, which include the ethanol to acid molar ratio, catalyst...

Full description

Bibliographic Details
Main Authors: Prapaporn Prasertpong, Chawannat Jaroenkhasemmeesuk, John R. Regalbuto, Jeremiah Lipp, Nakorn Tippayawong
Format: Article
Language:English
Published: Elsevier 2020-11-01
Series:Energy Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2352484719308285
_version_ 1818721081061539840
author Prapaporn Prasertpong
Chawannat Jaroenkhasemmeesuk
John R. Regalbuto
Jeremiah Lipp
Nakorn Tippayawong
author_facet Prapaporn Prasertpong
Chawannat Jaroenkhasemmeesuk
John R. Regalbuto
Jeremiah Lipp
Nakorn Tippayawong
author_sort Prapaporn Prasertpong
collection DOAJ
description In this work, the catalytic upgrading of a bio-oil model compound via esterification with ethanol was studied using 12-tungstosilicic acid as the catalyst. The response surface method was used to investigate and optimize the process variables, which include the ethanol to acid molar ratio, catalyst loading, reaction temperature, and reaction time for maximum conversion of the organic acid for esterification under atmospheric conditions. The effect of high He pressure on acid conversion for esterification was also studied. The maximum acid conversion was almost 90%, which can be achieved at reaction temperature of 77 °C, ethanol to acid molar ratio of 5:1, catalyst loading of 4.0% w/w, and reaction time of 8.3 h. Pressurizing the reaction with inert He did not have any effect for acid conversion at this optimum condition and had a slight negative effect under the studied conditions. After upgrading, the esterified products were found to improve the heating value from 17.6 to 23.2 MJ/kg and appeared to enhance fuel properties.
first_indexed 2024-12-17T20:33:03Z
format Article
id doaj.art-48f7b62c40ac475aaabf02c09bf7be33
institution Directory Open Access Journal
issn 2352-4847
language English
last_indexed 2024-12-17T20:33:03Z
publishDate 2020-11-01
publisher Elsevier
record_format Article
series Energy Reports
spelling doaj.art-48f7b62c40ac475aaabf02c09bf7be332022-12-21T21:33:31ZengElsevierEnergy Reports2352-48472020-11-01619Optimization of process variables for esterification of bio-oil model compounds by a heteropolyacid catalystPrapaporn Prasertpong0Chawannat Jaroenkhasemmeesuk1John R. Regalbuto2Jeremiah Lipp3Nakorn Tippayawong4Department of Mechanical Engineering, Faculty of Engineering, Chiang Mai University, Chiang Mai, 50200, ThailandDepartment of Mechanical Engineering, Faculty of Engineering, Mahidol University, Nakhon Pathom, 73170, ThailandDepartment of Chemical Engineering, University of South Carolina, Columbia, SC, 29201, United StatesDepartment of Chemical Engineering, University of South Carolina, Columbia, SC, 29201, United StatesDepartment of Mechanical Engineering, Faculty of Engineering, Chiang Mai University, Chiang Mai, 50200, Thailand; Corresponding author.In this work, the catalytic upgrading of a bio-oil model compound via esterification with ethanol was studied using 12-tungstosilicic acid as the catalyst. The response surface method was used to investigate and optimize the process variables, which include the ethanol to acid molar ratio, catalyst loading, reaction temperature, and reaction time for maximum conversion of the organic acid for esterification under atmospheric conditions. The effect of high He pressure on acid conversion for esterification was also studied. The maximum acid conversion was almost 90%, which can be achieved at reaction temperature of 77 °C, ethanol to acid molar ratio of 5:1, catalyst loading of 4.0% w/w, and reaction time of 8.3 h. Pressurizing the reaction with inert He did not have any effect for acid conversion at this optimum condition and had a slight negative effect under the studied conditions. After upgrading, the esterified products were found to improve the heating value from 17.6 to 23.2 MJ/kg and appeared to enhance fuel properties.http://www.sciencedirect.com/science/article/pii/S2352484719308285BiomassCatalytic upgradingDesign of experimentsPyrolysis oilRenewable energy
spellingShingle Prapaporn Prasertpong
Chawannat Jaroenkhasemmeesuk
John R. Regalbuto
Jeremiah Lipp
Nakorn Tippayawong
Optimization of process variables for esterification of bio-oil model compounds by a heteropolyacid catalyst
Energy Reports
Biomass
Catalytic upgrading
Design of experiments
Pyrolysis oil
Renewable energy
title Optimization of process variables for esterification of bio-oil model compounds by a heteropolyacid catalyst
title_full Optimization of process variables for esterification of bio-oil model compounds by a heteropolyacid catalyst
title_fullStr Optimization of process variables for esterification of bio-oil model compounds by a heteropolyacid catalyst
title_full_unstemmed Optimization of process variables for esterification of bio-oil model compounds by a heteropolyacid catalyst
title_short Optimization of process variables for esterification of bio-oil model compounds by a heteropolyacid catalyst
title_sort optimization of process variables for esterification of bio oil model compounds by a heteropolyacid catalyst
topic Biomass
Catalytic upgrading
Design of experiments
Pyrolysis oil
Renewable energy
url http://www.sciencedirect.com/science/article/pii/S2352484719308285
work_keys_str_mv AT prapapornprasertpong optimizationofprocessvariablesforesterificationofbiooilmodelcompoundsbyaheteropolyacidcatalyst
AT chawannatjaroenkhasemmeesuk optimizationofprocessvariablesforesterificationofbiooilmodelcompoundsbyaheteropolyacidcatalyst
AT johnrregalbuto optimizationofprocessvariablesforesterificationofbiooilmodelcompoundsbyaheteropolyacidcatalyst
AT jeremiahlipp optimizationofprocessvariablesforesterificationofbiooilmodelcompoundsbyaheteropolyacidcatalyst
AT nakorntippayawong optimizationofprocessvariablesforesterificationofbiooilmodelcompoundsbyaheteropolyacidcatalyst