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Synthesis and Properties of Dissymmetric Gemini Surfactants

A series of novel dissymmetric gemini cationics surfactants was synthesized by three-step reactions. The dissymmetric gemini surfactants contain a dodecanoic acid dimethylethylamine ester as the constant cationic part on one side of the hydroxypropyl center and a similar other cationic part, but wit...

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Detalles Bibliográficos
Autores principales: Xu, Qun, Wang, Liyan, Xing, Fenglan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3150800/
https://www.ncbi.nlm.nih.gov/pubmed/21841907
http://dx.doi.org/10.1007/s11743-010-1207-6
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author Xu, Qun
Wang, Liyan
Xing, Fenglan
author_facet Xu, Qun
Wang, Liyan
Xing, Fenglan
author_sort Xu, Qun
collection PubMed
description A series of novel dissymmetric gemini cationics surfactants was synthesized by three-step reactions. The dissymmetric gemini surfactants contain a dodecanoic acid dimethylethylamine ester as the constant cationic part on one side of the hydroxypropyl center and a similar other cationic part, but with a different acid length (from octanoic to palmitic), on the other side. The critical micelle concentration (CMC) and the effectiveness of surface tension reduction (γ (CMC)) were determined. The surface tension measurements of dissymmetric gemini surfactants showed good water solubility, and low CMC had great efficiency in lowering the surface tension and a strong adsorption at the air/water interface. The CMC was observed to increase initially with the increase of the ester bond alkyl group. They also showed good foaming properties and wetting capabilites.
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spelling pubmed-31508002011-08-10 Synthesis and Properties of Dissymmetric Gemini Surfactants Xu, Qun Wang, Liyan Xing, Fenglan J Surfactants Deterg Original Article A series of novel dissymmetric gemini cationics surfactants was synthesized by three-step reactions. The dissymmetric gemini surfactants contain a dodecanoic acid dimethylethylamine ester as the constant cationic part on one side of the hydroxypropyl center and a similar other cationic part, but with a different acid length (from octanoic to palmitic), on the other side. The critical micelle concentration (CMC) and the effectiveness of surface tension reduction (γ (CMC)) were determined. The surface tension measurements of dissymmetric gemini surfactants showed good water solubility, and low CMC had great efficiency in lowering the surface tension and a strong adsorption at the air/water interface. The CMC was observed to increase initially with the increase of the ester bond alkyl group. They also showed good foaming properties and wetting capabilites. Springer-Verlag 2010-05-26 2011 /pmc/articles/PMC3150800/ /pubmed/21841907 http://dx.doi.org/10.1007/s11743-010-1207-6 Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Article
Xu, Qun
Wang, Liyan
Xing, Fenglan
Synthesis and Properties of Dissymmetric Gemini Surfactants
title Synthesis and Properties of Dissymmetric Gemini Surfactants
title_full Synthesis and Properties of Dissymmetric Gemini Surfactants
title_fullStr Synthesis and Properties of Dissymmetric Gemini Surfactants
title_full_unstemmed Synthesis and Properties of Dissymmetric Gemini Surfactants
title_short Synthesis and Properties of Dissymmetric Gemini Surfactants
title_sort synthesis and properties of dissymmetric gemini surfactants
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3150800/
https://www.ncbi.nlm.nih.gov/pubmed/21841907
http://dx.doi.org/10.1007/s11743-010-1207-6
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