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Synthesis and Physical Properties of Estolide Ester Using Saturated Fatty Acid and Ricinoleic Acid

A study was conveyed to produce estolide ester using ricinoleic acid as the backbone. The ricinoleic acid reacted with saturated fatty acid from C8–C18. These reactions were conducted under vacuum at 60°C for 24 h without solvent. The reaction used acid catalyst, sulphuric acid. The new saturate ric...

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Detalles Bibliográficos
Autores principales: Salimon, Jumat, Nallathamby, Neeranjini, Salih, Nadia, Abdullah, Bashar Mudhaffar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3189567/
https://www.ncbi.nlm.nih.gov/pubmed/22007150
http://dx.doi.org/10.1155/2011/263624
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author Salimon, Jumat
Nallathamby, Neeranjini
Salih, Nadia
Abdullah, Bashar Mudhaffar
author_facet Salimon, Jumat
Nallathamby, Neeranjini
Salih, Nadia
Abdullah, Bashar Mudhaffar
author_sort Salimon, Jumat
collection PubMed
description A study was conveyed to produce estolide ester using ricinoleic acid as the backbone. The ricinoleic acid reacted with saturated fatty acid from C8–C18. These reactions were conducted under vacuum at 60°C for 24 h without solvent. The reaction used acid catalyst, sulphuric acid. The new saturate ricinoleic estolide esters show superior low-temperature properties (−52 ± 0.08°C) and high flash point (>300°C). The yield of the neat estolide esters ranged from 52% to 96%. The viscosity range was 51 ± 0.08 to 86 ± 0.01 cp. These new saturated estolide esters were also compared with saturated branched estolide esters.
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spelling pubmed-31895672011-10-17 Synthesis and Physical Properties of Estolide Ester Using Saturated Fatty Acid and Ricinoleic Acid Salimon, Jumat Nallathamby, Neeranjini Salih, Nadia Abdullah, Bashar Mudhaffar J Autom Methods Manag Chem Research Article A study was conveyed to produce estolide ester using ricinoleic acid as the backbone. The ricinoleic acid reacted with saturated fatty acid from C8–C18. These reactions were conducted under vacuum at 60°C for 24 h without solvent. The reaction used acid catalyst, sulphuric acid. The new saturate ricinoleic estolide esters show superior low-temperature properties (−52 ± 0.08°C) and high flash point (>300°C). The yield of the neat estolide esters ranged from 52% to 96%. The viscosity range was 51 ± 0.08 to 86 ± 0.01 cp. These new saturated estolide esters were also compared with saturated branched estolide esters. Hindawi Publishing Corporation 2011 2011-10-05 /pmc/articles/PMC3189567/ /pubmed/22007150 http://dx.doi.org/10.1155/2011/263624 Text en Copyright © 2011 Jumat Salimon et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Salimon, Jumat
Nallathamby, Neeranjini
Salih, Nadia
Abdullah, Bashar Mudhaffar
Synthesis and Physical Properties of Estolide Ester Using Saturated Fatty Acid and Ricinoleic Acid
title Synthesis and Physical Properties of Estolide Ester Using Saturated Fatty Acid and Ricinoleic Acid
title_full Synthesis and Physical Properties of Estolide Ester Using Saturated Fatty Acid and Ricinoleic Acid
title_fullStr Synthesis and Physical Properties of Estolide Ester Using Saturated Fatty Acid and Ricinoleic Acid
title_full_unstemmed Synthesis and Physical Properties of Estolide Ester Using Saturated Fatty Acid and Ricinoleic Acid
title_short Synthesis and Physical Properties of Estolide Ester Using Saturated Fatty Acid and Ricinoleic Acid
title_sort synthesis and physical properties of estolide ester using saturated fatty acid and ricinoleic acid
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3189567/
https://www.ncbi.nlm.nih.gov/pubmed/22007150
http://dx.doi.org/10.1155/2011/263624
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