Catalytic epoxidation of unsaturated fatty acids in palm stearin via in situ peracetic acids mechanism

Epoxidized vegetable oils present a viable substitute for polymers derived from petroleum. This research focuses on the impact of a process parameter on the epoxidation of palm stearin when zeolite ZSM-5 is used as a catalyst. This study synthesized peracetic acid as the oxidizing agent by combining...

Full description

Bibliographic Details
Published in:Scientific Reports
Main Author: Rahim N.H.; Jalil M.J.; Mubarak N.M.; Azmi I.S.; Anbuchezhiyan G.
Format: Article
Language:English
Published: Nature Research 2025
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85218207572&doi=10.1038%2fs41598-025-89399-x&partnerID=40&md5=b159e71f6a87fddd43d21a9845e25d70
id 2-s2.0-85218207572
spelling 2-s2.0-85218207572
Rahim N.H.; Jalil M.J.; Mubarak N.M.; Azmi I.S.; Anbuchezhiyan G.
Catalytic epoxidation of unsaturated fatty acids in palm stearin via in situ peracetic acids mechanism
2025
Scientific Reports
15
1
10.1038/s41598-025-89399-x
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85218207572&doi=10.1038%2fs41598-025-89399-x&partnerID=40&md5=b159e71f6a87fddd43d21a9845e25d70
Epoxidized vegetable oils present a viable substitute for polymers derived from petroleum. This research focuses on the impact of a process parameter on the epoxidation of palm stearin when zeolite ZSM-5 is used as a catalyst. This study synthesized peracetic acid as the oxidizing agent by combining hydrogen peroxide and acetic acid, adjusting molar ratios relative to palm stearin. The optimal relative conversion oxirane (RCO) percentage reached 43.06% at 70 °C, 200 rpm stirring speed, and 0.8 g of catalyst. The acetic acid to palm stearin molar ratio was 1:1, and the hydrogen peroxide to palm stearin ratio was 0.5:1. Both palm stearin and its epoxide derivative have been studied using Fourier-transform infrared spectroscopy, showing the appearance of an oxirane ring at a wavenumber of 1240 cm⁻¹. Kinetic modelling demonstrates that the simulation and experiment show a reasonable discrepancy, considering several assumptions that have been made. After 100 iterations, the reaction rate constant obtained as follows: =0.01 mol⋅L−1⋅min−1, = 1.85 mol⋅L−1⋅min−1, = 29.90 mol⋅L− 1⋅min− 1, and = 0.04 mol⋅L−1⋅min−1. © The Author(s) 2025.
Nature Research
20452322
English
Article

author Rahim N.H.; Jalil M.J.; Mubarak N.M.; Azmi I.S.; Anbuchezhiyan G.
spellingShingle Rahim N.H.; Jalil M.J.; Mubarak N.M.; Azmi I.S.; Anbuchezhiyan G.
Catalytic epoxidation of unsaturated fatty acids in palm stearin via in situ peracetic acids mechanism
author_facet Rahim N.H.; Jalil M.J.; Mubarak N.M.; Azmi I.S.; Anbuchezhiyan G.
author_sort Rahim N.H.; Jalil M.J.; Mubarak N.M.; Azmi I.S.; Anbuchezhiyan G.
title Catalytic epoxidation of unsaturated fatty acids in palm stearin via in situ peracetic acids mechanism
title_short Catalytic epoxidation of unsaturated fatty acids in palm stearin via in situ peracetic acids mechanism
title_full Catalytic epoxidation of unsaturated fatty acids in palm stearin via in situ peracetic acids mechanism
title_fullStr Catalytic epoxidation of unsaturated fatty acids in palm stearin via in situ peracetic acids mechanism
title_full_unstemmed Catalytic epoxidation of unsaturated fatty acids in palm stearin via in situ peracetic acids mechanism
title_sort Catalytic epoxidation of unsaturated fatty acids in palm stearin via in situ peracetic acids mechanism
publishDate 2025
container_title Scientific Reports
container_volume 15
container_issue 1
doi_str_mv 10.1038/s41598-025-89399-x
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85218207572&doi=10.1038%2fs41598-025-89399-x&partnerID=40&md5=b159e71f6a87fddd43d21a9845e25d70
description Epoxidized vegetable oils present a viable substitute for polymers derived from petroleum. This research focuses on the impact of a process parameter on the epoxidation of palm stearin when zeolite ZSM-5 is used as a catalyst. This study synthesized peracetic acid as the oxidizing agent by combining hydrogen peroxide and acetic acid, adjusting molar ratios relative to palm stearin. The optimal relative conversion oxirane (RCO) percentage reached 43.06% at 70 °C, 200 rpm stirring speed, and 0.8 g of catalyst. The acetic acid to palm stearin molar ratio was 1:1, and the hydrogen peroxide to palm stearin ratio was 0.5:1. Both palm stearin and its epoxide derivative have been studied using Fourier-transform infrared spectroscopy, showing the appearance of an oxirane ring at a wavenumber of 1240 cm⁻¹. Kinetic modelling demonstrates that the simulation and experiment show a reasonable discrepancy, considering several assumptions that have been made. After 100 iterations, the reaction rate constant obtained as follows: =0.01 mol⋅L−1⋅min−1, = 1.85 mol⋅L−1⋅min−1, = 29.90 mol⋅L− 1⋅min− 1, and = 0.04 mol⋅L−1⋅min−1. © The Author(s) 2025.
publisher Nature Research
issn 20452322
language English
format Article
accesstype
record_format scopus
collection Scopus
_version_ 1825722572490145792