2017
DOI: 10.1016/j.indcrop.2017.04.005
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Synthesis of 10-undecenoic acid based C 22 -dimer acid esters and their evaluation as potential lubricant basestocks

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Cited by 28 publications
(26 citation statements)
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“…Various green technologies for esterification have been investigated including self‐esterification, heterogeneous catalysis, and enzymatic reactions, and there are several previous studies highlighting solvent‐free esterification for biolubricant production . However, to the best of our knowledge, most of DFAEs are produced by esterification of dimer acid and alcohol catalyzed by organic acid such as p ‐toluenesulfonic acid, or dimerization of methyl ester of fatty acids .…”
Section: Introductionmentioning
confidence: 99%
“…Various green technologies for esterification have been investigated including self‐esterification, heterogeneous catalysis, and enzymatic reactions, and there are several previous studies highlighting solvent‐free esterification for biolubricant production . However, to the best of our knowledge, most of DFAEs are produced by esterification of dimer acid and alcohol catalyzed by organic acid such as p ‐toluenesulfonic acid, or dimerization of methyl ester of fatty acids .…”
Section: Introductionmentioning
confidence: 99%
“…Substantial progress in the development of industrial and consumer goods based from biorefineries includes broad based biolubricants base oils containing furan ring and branched chain alkanes from oleic acid, milkweed oil, cotton seed oil, canola oil ricinoleic acid from soybean bean. Chemical and enzymatic modification of these renewable materials have led to commercial production of renewable lubricant base oil, cold flow imoprover additives, "green diesel, " surface active agents and rusty and corrosion inhibitors (Adhvaryu et al, 2000;Seo et al, 2012;Yasa et al, 2017;Dunn et al, 2019;Liu et al, 2019).…”
Section: Platform Chemicals From Cellulose and Hemicellulosementioning
confidence: 99%
“…Current advancements in green chemistry and bio-based technologies have given rise to new players among dibasic esters. High-temperature reactions over montmorillonite clay can produce a mix of methyl-branched C22 alpha,omega-dicarboxylic acids, which can be turned into dibasic esters [1]. For feedstock, 11-undecenoic acid is used, yielding trans double bonds.…”
Section: Heat-thinning Of Unsaturated Estersmentioning
confidence: 99%