2017
DOI: 10.1016/j.jart.2016.12.004
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Convenient synthesis, characterization and surface active properties of novel cationic gemini surfactants with carbonate linkage based on C 12 C 18 sat./unsat. fatty acids

Abstract: Convenient synthesis, characterization and surface active properties of novel cationic gemini surfactants with carbonate linkage based on C 12 C 18 sat./unsat. fatty acids

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Cited by 13 publications
(13 citation statements)
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“…b, the most abundant FA in mono‐AE were 16:0 (59.97%) and 18:0 (40.03%) in photoautotrophic cells. Because the fatty acid obtained under this condition did not possess double bonds (i.e., 16:0 and 18:0 only), it would be very useful as a feedstock for surfactant synthesis (Tripathy and Mishra, ). Interestingly, under heterotrophic conditions fed with 30 g L −1 glucose, the percentage of 18:1 in FA in mono‐AE also increased remarkably from 0% to 14.84%.…”
Section: Resultsmentioning
confidence: 99%
“…b, the most abundant FA in mono‐AE were 16:0 (59.97%) and 18:0 (40.03%) in photoautotrophic cells. Because the fatty acid obtained under this condition did not possess double bonds (i.e., 16:0 and 18:0 only), it would be very useful as a feedstock for surfactant synthesis (Tripathy and Mishra, ). Interestingly, under heterotrophic conditions fed with 30 g L −1 glucose, the percentage of 18:1 in FA in mono‐AE also increased remarkably from 0% to 14.84%.…”
Section: Resultsmentioning
confidence: 99%
“…The microwave synthesized the surfactant in 5-10 minutes with a better yield of 80-91% as compared to conventional method i.e. thermal condensation which produced 75-80% [19][20][21][22]. The comparative study has also been done by Jianbin Huang on gemini and Bola, and the role of cephalic groups was found to be important as they alter their properties.…”
Section: Imidazolinium Gemini Surfactantsmentioning
confidence: 99%
“…Tripathy et al (2016) synthesized gemini imidazoline by the reaction of monomeric imidazoline and di iodoalkyl carbonated under microwave irradiation. Synthesis of di (iodoethyl) carbonate as quaternizing has been achieved by mixing the iodo alkanol and diphenyl carbonate (1:2 molar ratio) acted as carbonate exchange reaction in acetone at room temperature [22]. The resultant product was recrystallized by adding ethyl acetate and acetone (50:50) in it.…”
Section: Synthesis Of Cationic Gemini Imidazoline Surfactants With Camentioning
confidence: 99%
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