Synergistic hybrid catalyst synthesis for epoxidation of linoleic acid via in situ performic acid
This study aims to investigate the optimal conditions for the epoxidation of linoleic acid by an in situ peracid mechanism with an applied hybrid sulfuric and hydrochloric acid as catalysts. There is no published work on producing epoxidized linoleic acid by peracetic acid mechanism using a hybrid h...
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Springer Science and Business Media Deutschland GmbH
2024
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2-s2.0-85190394748 Shahrizan A.S.A.; Azmi I.S.; Mubarak N.M.; Jalil M.J. Synergistic hybrid catalyst synthesis for epoxidation of linoleic acid via in situ performic acid 2024 Biomass Conversion and Biorefinery 10.1007/s13399-024-05601-6 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85190394748&doi=10.1007%2fs13399-024-05601-6&partnerID=40&md5=506fb117b4b3ff4a4b064808f3afd012 This study aims to investigate the optimal conditions for the epoxidation of linoleic acid by an in situ peracid mechanism with an applied hybrid sulfuric and hydrochloric acid as catalysts. There is no published work on producing epoxidized linoleic acid by peracetic acid mechanism using a hybrid homogenous-homogenous catalyst. The linoleic acid was epoxidized with performic acid obtained in situ through the reaction between formic acid and hydrogen peroxide in the presence of a catalyst. The highest conversion to oxirane of 85% was achieved at a ratio of 1 M formic acid to 2 M of hydrogen peroxide, a temperature of 45 °C, and a stirring speed of 400 rpm. The characterization using a Fourier-transform infrared spectroscopy (FTIR) shows the existence of the oxirane ring group at wavenumber 860 cm−1. The numerical simulations were performed using a genetic algorithm, and the results showed good agreement between the simulation and experimental data, which validates the kinetic model. © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2024. Springer Science and Business Media Deutschland GmbH 21906815 English Article |
author |
Shahrizan A.S.A.; Azmi I.S.; Mubarak N.M.; Jalil M.J. |
spellingShingle |
Shahrizan A.S.A.; Azmi I.S.; Mubarak N.M.; Jalil M.J. Synergistic hybrid catalyst synthesis for epoxidation of linoleic acid via in situ performic acid |
author_facet |
Shahrizan A.S.A.; Azmi I.S.; Mubarak N.M.; Jalil M.J. |
author_sort |
Shahrizan A.S.A.; Azmi I.S.; Mubarak N.M.; Jalil M.J. |
title |
Synergistic hybrid catalyst synthesis for epoxidation of linoleic acid via in situ performic acid |
title_short |
Synergistic hybrid catalyst synthesis for epoxidation of linoleic acid via in situ performic acid |
title_full |
Synergistic hybrid catalyst synthesis for epoxidation of linoleic acid via in situ performic acid |
title_fullStr |
Synergistic hybrid catalyst synthesis for epoxidation of linoleic acid via in situ performic acid |
title_full_unstemmed |
Synergistic hybrid catalyst synthesis for epoxidation of linoleic acid via in situ performic acid |
title_sort |
Synergistic hybrid catalyst synthesis for epoxidation of linoleic acid via in situ performic acid |
publishDate |
2024 |
container_title |
Biomass Conversion and Biorefinery |
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container_issue |
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doi_str_mv |
10.1007/s13399-024-05601-6 |
url |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85190394748&doi=10.1007%2fs13399-024-05601-6&partnerID=40&md5=506fb117b4b3ff4a4b064808f3afd012 |
description |
This study aims to investigate the optimal conditions for the epoxidation of linoleic acid by an in situ peracid mechanism with an applied hybrid sulfuric and hydrochloric acid as catalysts. There is no published work on producing epoxidized linoleic acid by peracetic acid mechanism using a hybrid homogenous-homogenous catalyst. The linoleic acid was epoxidized with performic acid obtained in situ through the reaction between formic acid and hydrogen peroxide in the presence of a catalyst. The highest conversion to oxirane of 85% was achieved at a ratio of 1 M formic acid to 2 M of hydrogen peroxide, a temperature of 45 °C, and a stirring speed of 400 rpm. The characterization using a Fourier-transform infrared spectroscopy (FTIR) shows the existence of the oxirane ring group at wavenumber 860 cm−1. The numerical simulations were performed using a genetic algorithm, and the results showed good agreement between the simulation and experimental data, which validates the kinetic model. © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2024. |
publisher |
Springer Science and Business Media Deutschland GmbH |
issn |
21906815 |
language |
English |
format |
Article |
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record_format |
scopus |
collection |
Scopus |
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1809677774934245376 |