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Comparison of different heterogeneous catalysts for the estolides synthesis from oleic acid

Mohamad Nordin, Nor Asikin and Adnan, Nadia Farhana and Hamzah, Noraini and Wan Isahak, Wan Nor Roslam and Ayatillah, Alifee and Salimon, Jumat and Yarmo, Mohd. Ambar and Kamaruddin, Rose Aini (2012) Comparison of different heterogeneous catalysts for the estolides synthesis from oleic acid. In: International Conference for Nanomaterials Synthesis and Characterization. Trans Tech Publications, Switzerland, pp. 288-292. ISBN 978-303785301-6

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Official URL: http://dx.doi.org/10.4028/www.scientific.net/AMR.3...

Abstract

Different catalysts, namely various loading of perchloric acid on various supports; HClO 4/silica (SiO 2), HClO 4/silica gel (SG) and HClO 4/alumina (Al 2O 3) were tested for the direct addition reaction of oleic acid (OA) to form estolide compounds. The reactions were carried out under vacuum (2 mBar) for 10 hours at 70 °C under solvent-less conditions. LC-MS ToF of reaction products results showed chromatographic peaks for the presence of two new estolide compounds, oleic-oleic monoestolide acid (m/z 563.51, as [M-H]-), and oleic-oleic diestolide acid (m/z 845.77 [M-H]-). The optimum loading of HClO 4 for every support are 15 wt.% HClO 4/SiO 2 (SiO 215), 10 wt.% HClO 4/SG (SG10) and 35 wt.% HClO 4/Al 2O 3 (Al 2O 335). The SG10 turned out to be the best catalyst, achieving a final conversion of 97.5 % with 79.8 % selectivity to oleic-oleic monoestolide acid and 17.7 % selectivity to oleic-oleic diestolide acid. The activity and selectivity of the SG10 have been investigated and compared with homogeneous HClO 4. The optimum catalysts for every support were characterized by XPS analysis, BET, TEM and TPD-NH 3.

Item Type:Book Section
Additional Information:Indexed by Web of Science
Uncontrolled Keywords:estolide synthesis, oleic acid, silica, silica gel, alumina
Subjects:Q Science > Q Science (General)
Divisions:Others
ID Code:34554
Deposited By:INVALID USER
Deposited On:09 Oct 2013 06:44
Last Modified:02 Feb 2017 05:53

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