BibTex Citation Data :
@article{Reaktor9835, author = {Maisaroh Maisaroh and Indra Budi Susetyo and Bayu Rusmandana}, title = {SINTESIS ASAM 9,10-DIHIDROKSI STEARAT (DHSA) MELALUI HIDROLISA EPOKSIDA DARI OKSIDASI ASAM OLEAT DENGAN ASAM PERFORMAT}, journal = {Reaktor}, volume = {16}, number = {2}, year = {2016}, keywords = {Process}, abstract = { SYNTHESIS OF 9,10-DIHYDROXYSTEARIC ACID (DHSA) THROUGH HYDROLYSIS EPOXIDE FROM OXIDATION OLEIC ACID AND PERFORMIC ACID. 9,10-dihydroxy stearic acid (DHSA) ; C 18 H 36 O 4 is one of hydroxyl fatty acid s with hydroxyl groups (OH) and carboxyl groups (-COOH) cause DHSA have unique properties for many applications including as an emulsifier in the oil phase/gel candles and water in cosmetic formulations. This study investigated the formation of DHSA of from oleic acid and performic acid through epoxidation and hydrolysis reactions. Epoxidation was carried out by reacting the oleic acid with formic acid to form performic acid in situ reaction at a temperature of 60-70 o C with stirring in order to minimize byproduct , followed hydrolysis obtained DHSA as powder with melting point 86.5 o C, iodine value 0.125 g I 2 /100 g, acid value 171.53 mg KOH/g, the hydroxyl group observed at the absorption band region of 3 345.34 cm -1 , LCMS analysis results show peak spetrograms-mass at m/z 317,269, with a value m/z is equivalent to molecular weight DHSA. Keywords: DHSA; epoxidation; hydrolysis ; hydroxyl fatty acids; oleic acid Abstrak Asam 9,10-dihidroksi stearat (DHSA) dengan rumus molekul C 18 H 36 O 4 merupakan senyawa hidroksil asam lemak dengan gugus hidroksil (-OH) dan karboksil (-COOH) menyebabkan DHSA memiliki sifat unik untuk berbagai aplikasi antara lain sebagai emulsifier antara fasa minyak/lilin gel dan air dalam formulasi kosmetik. Penelitian ini bertujuan untuk menghasilkan DHSA dari asam oleat dan asam performat, melalui tahapan reaksi epoksidasi dan hidrolisa. Epoksidasi asam oleat dengan asam performat yang dibentuk secara in situ dilakukan pada suhu reaksi 60-70 o C dengan pengadukan untuk meminimalkan reaksi samping, dilanjutkan dengan hidrolisa epoksida diperoleh DHSA berupa serbuk berwarna putih gading dengan titik leleh 86,5 o C, bilangan iod ± 0,125 g I 2 /100 g, bilangan asam 171,53 mg KOH/g, gugus hidroksil teramati menggunakan FTIR pada bilangan gelombang 3345,34 cm -1 , yang diperkuat dengan data kromatogram LC-MS yang memberikan puncak spektrogram-massa pada m/z 317.269, dengan harga m/z yang setara dengan Berat Molekul DHSA. Kata kunci: DHSA; epoksidasi; hidrolisa; hidroksil asam lemak; asam oleat }, issn = {2407-5973}, pages = {57--64} doi = {10.14710/reaktor.16.2.57-64}, url = {https://ejournal.undip.ac.id/index.php/reaktor/article/view/9835} }
Refworks Citation Data :
SYNTHESIS OF 9,10-DIHYDROXYSTEARIC ACID (DHSA) THROUGH HYDROLYSIS EPOXIDE FROM OXIDATION OLEIC ACID AND PERFORMIC ACID. 9,10-dihydroxy stearic acid (DHSA); C18H36O4 is one of hydroxyl fatty acids with hydroxyl groups (OH) and carboxyl groups (-COOH) cause DHSA have unique properties for many applications including as an emulsifier in the oil phase/gel candles and water in cosmetic formulations. This study investigated the formation of DHSA of from oleic acid and performic acid through epoxidation and hydrolysis reactions. Epoxidation was carried out by reacting the oleic acid with formic acid to form performic acid in situ reaction at a temperature of 60-70oC with stirring in order to minimize byproduct, followed hydrolysis obtained DHSA as powder with melting point 86.5oC, iodine value 0.125 g I2/100 g, acid value 171.53 mg KOH/g, the hydroxyl group observed at the absorption band region of 3345.34 cm-1, LCMS analysis results show peak spetrograms-mass at m/z 317,269, with a value m/z is equivalent to molecular weight DHSA.
Keywords: DHSA; epoxidation; hydrolysis; hydroxyl fatty acids; oleic acid
Abstrak
Asam 9,10-dihidroksi stearat (DHSA) dengan rumus molekul C18H36O4 merupakan senyawa hidroksil asam lemak dengan gugus hidroksil (-OH) dan karboksil (-COOH) menyebabkan DHSA memiliki sifat unik untuk berbagai aplikasi antara lain sebagai emulsifier antara fasa minyak/lilin gel dan air dalam formulasi kosmetik. Penelitian ini bertujuan untuk menghasilkan DHSA dari asam oleat dan asam performat, melalui tahapan reaksi epoksidasi dan hidrolisa. Epoksidasi asam oleat dengan asam performat yang dibentuk secara in situ dilakukan pada suhu reaksi 60-70oC dengan pengadukan untuk meminimalkan reaksi samping, dilanjutkan dengan hidrolisa epoksida diperoleh DHSA berupa serbuk berwarna putih gading dengan titik leleh 86,5oC, bilangan iod ± 0,125 g I2/100 g, bilangan asam 171,53 mg KOH/g, gugus hidroksil teramati menggunakan FTIR pada bilangan gelombang 3345,34 cm-1, yang diperkuat dengan data kromatogram LC-MS yang memberikan puncak spektrogram-massa pada m/z 317.269, dengan harga m/z yang setara dengan Berat Molekul DHSA.
Kata kunci: DHSA; epoksidasi; hidrolisa; hidroksil asam lemak; asam oleat
Note: This article has supplementary file(s).
Article Metrics:
Last update:
Utilization of fatty acid from papaya seed waste oil (carica papaya l) as a raw material in the making of epoxy compound
Proceedings of the 2nd International Conference on Science Education and Sciences 2022 (ICSES 2022)
Last update: 2025-01-14 22:32:31
In order for REAKTOR to publish and disseminate research articles, we need non-exclusive publishing rights (transferred from the author(s) to the publisher). This is determined by a publishing agreement between the Author(s) and REAKTOR. This agreement deals with transferring or licensing the publishing copyright to REAKTOR while Authors still retain significant rights to use and share their published articles. REAKTOR supports the need for authors to share, disseminate, and maximize the impact of their research and these rights in any databases.
As a journal author, you have the right to use your article for many purposes, including by your employing institute or company. These Author rights can be exercised without the need to obtain specific permission. Authors publishing in BCREC journals have wide rights to use their works for teaching and scholarly purposes without needing to seek permission, including, but not limited to:
Authors/Readers/Third Parties can copy and redistribute the material in any medium or format and remix, transform, and build upon the material for any purpose, even commercially. Still, they must give appropriate credit (the name of the creator and attribution parties (authors detail information), a copyright notice, an open access license notice, a disclaimer notice, and a link to the material), provide a link to the license, and indicate if changes were made (Publisher indicates the modification of the material (if any).
Authors/Readers/Third Parties can read, print and download, redistribute or republish the article (e.g., display in a repository), translate the article, download for text and data mining purposes, reuse portions or extracts from the article in other works, sell or re-use for commercial purposes, remix, transform, or build upon the material, they must distribute their contributions under the same license as the original Creative Commons Attribution-ShareAlike (CC BY-SA).
JURNAL REAKTOR (p-ISSN: 0852-0798; e-ISSN: 2407-5973)
Published by Departement of Chemical Engineering, Diponegoro University