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Biolubricant basestocks from chemically modified plant oils: ricinoleic acid based-tetraesters
BACKGROUND: Plant oils have been investigated as a potential source of environmentally favorable biolubricants because of their biodegradability, renewability and excellent lubrication performance. Low oxidation and thermal stability, poor low-temperature properties and a narrow range of available v...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3726387/ https://www.ncbi.nlm.nih.gov/pubmed/23885790 http://dx.doi.org/10.1186/1752-153X-7-128 |
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author | Salih, Nadia Salimon, Jumat Yousif, Emad Abdullah, Bashar Mudhaffar |
author_facet | Salih, Nadia Salimon, Jumat Yousif, Emad Abdullah, Bashar Mudhaffar |
author_sort | Salih, Nadia |
collection | PubMed |
description | BACKGROUND: Plant oils have been investigated as a potential source of environmentally favorable biolubricants because of their biodegradability, renewability and excellent lubrication performance. Low oxidation and thermal stability, poor low-temperature properties and a narrow range of available viscosities, however, limit their potential application as industrial lubricants. The inherent problems of plant oils can be improved by attaching functional groups at the sites of unsaturation through chemical modifications. In this article, we will demonstrate how functionalization helps overcome these disadvantages. RESULTS: In this work, mono-, tri- and tetra-esters have been synthesized, including 10,12-dihydroxy-9-(stearoyloxy)octadecanoic acid 3; 9,10,12-tris(stearoyloxy)octadecanoic acid 4; and 18-(4-ethylhexyloxy)-18-oxooctadecane-7,9,10-triyl tristearate 5. Pour-point and cloud-point measurements have shown that these derivatives have improved low-temperature properties as compared to the precursor. The tetra ester compound, 18-(4-ethylhexyloxy)-18-oxooctadecane-7,9,10-triyl tristearate 5, had the lowest pour point (PP) (−44.37°C) and the lowest cloud point (CP) (−41.25°C). This derivatization also improved the compound’s thermo-oxidative stability, measured using pressurized differential scanning calorimetry (PDSC) and thin-film micro-oxidation (TFMO) testing. 18-(4-Ethylhexyloxy)-18-oxooctadecane-7,9,10-triyl tristearate 5 also had the highest onset temperature (OT) (282.10°C) and the lowest volatile loss and insoluble deposit (37.39% and 50.87%, respectively). Furthermore, the compounds’ tribological behaviors were evaluated using the four-ball method. 18-(4-Ethylhexyloxy)-18-oxooctadecane-7,9,10-triyl tristearate 5 also had the lowest coefficient of friction (μ) (0.44). CONCLUSIONS: The results showed that, in general, these derivatives have good anti-wear and friction-reducing properties at relatively low concentrations under all of the test loads. Overall, the data indicates that these derivatives have significant potential to be used as biolubricant basestocks. |
format | Online Article Text |
id | pubmed-3726387 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-37263872013-07-30 Biolubricant basestocks from chemically modified plant oils: ricinoleic acid based-tetraesters Salih, Nadia Salimon, Jumat Yousif, Emad Abdullah, Bashar Mudhaffar Chem Cent J Research Article BACKGROUND: Plant oils have been investigated as a potential source of environmentally favorable biolubricants because of their biodegradability, renewability and excellent lubrication performance. Low oxidation and thermal stability, poor low-temperature properties and a narrow range of available viscosities, however, limit their potential application as industrial lubricants. The inherent problems of plant oils can be improved by attaching functional groups at the sites of unsaturation through chemical modifications. In this article, we will demonstrate how functionalization helps overcome these disadvantages. RESULTS: In this work, mono-, tri- and tetra-esters have been synthesized, including 10,12-dihydroxy-9-(stearoyloxy)octadecanoic acid 3; 9,10,12-tris(stearoyloxy)octadecanoic acid 4; and 18-(4-ethylhexyloxy)-18-oxooctadecane-7,9,10-triyl tristearate 5. Pour-point and cloud-point measurements have shown that these derivatives have improved low-temperature properties as compared to the precursor. The tetra ester compound, 18-(4-ethylhexyloxy)-18-oxooctadecane-7,9,10-triyl tristearate 5, had the lowest pour point (PP) (−44.37°C) and the lowest cloud point (CP) (−41.25°C). This derivatization also improved the compound’s thermo-oxidative stability, measured using pressurized differential scanning calorimetry (PDSC) and thin-film micro-oxidation (TFMO) testing. 18-(4-Ethylhexyloxy)-18-oxooctadecane-7,9,10-triyl tristearate 5 also had the highest onset temperature (OT) (282.10°C) and the lowest volatile loss and insoluble deposit (37.39% and 50.87%, respectively). Furthermore, the compounds’ tribological behaviors were evaluated using the four-ball method. 18-(4-Ethylhexyloxy)-18-oxooctadecane-7,9,10-triyl tristearate 5 also had the lowest coefficient of friction (μ) (0.44). CONCLUSIONS: The results showed that, in general, these derivatives have good anti-wear and friction-reducing properties at relatively low concentrations under all of the test loads. Overall, the data indicates that these derivatives have significant potential to be used as biolubricant basestocks. BioMed Central 2013-07-25 /pmc/articles/PMC3726387/ /pubmed/23885790 http://dx.doi.org/10.1186/1752-153X-7-128 Text en Copyright © 2013 Salih et al.; licensee Chemistry Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Salih, Nadia Salimon, Jumat Yousif, Emad Abdullah, Bashar Mudhaffar Biolubricant basestocks from chemically modified plant oils: ricinoleic acid based-tetraesters |
title | Biolubricant basestocks from chemically modified plant oils: ricinoleic acid based-tetraesters |
title_full | Biolubricant basestocks from chemically modified plant oils: ricinoleic acid based-tetraesters |
title_fullStr | Biolubricant basestocks from chemically modified plant oils: ricinoleic acid based-tetraesters |
title_full_unstemmed | Biolubricant basestocks from chemically modified plant oils: ricinoleic acid based-tetraesters |
title_short | Biolubricant basestocks from chemically modified plant oils: ricinoleic acid based-tetraesters |
title_sort | biolubricant basestocks from chemically modified plant oils: ricinoleic acid based-tetraesters |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3726387/ https://www.ncbi.nlm.nih.gov/pubmed/23885790 http://dx.doi.org/10.1186/1752-153X-7-128 |
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