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Synthesis and Surface Active Properties of a Novel Linear Dodecyl Diphenyl Ether Sulfonate Gemini Surfactant

The linear dodecyl diphenyl ether sulfonate gemini surfactant (C 12 -DLADS) has been synthesized by a new route from lauric acid according to a five-step reaction sequence consisting of acidification, Friedel–Crafts acylation, Clemmensen reduction, sulfonation and a neutralization reaction. The surf...

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Bibliographic Details
Published in:Journal of surfactants and detergents 2012-11, Vol.15 (6), p.703-707
Main Authors: Hujun, Xu, Qicheng, Liu, Dandan, Chen, Xiaoya, Liu
Format: Article
Language:English
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Summary:The linear dodecyl diphenyl ether sulfonate gemini surfactant (C 12 -DLADS) has been synthesized by a new route from lauric acid according to a five-step reaction sequence consisting of acidification, Friedel–Crafts acylation, Clemmensen reduction, sulfonation and a neutralization reaction. The surfactant and intermediates were characterized by 1 H-NMR, HPLC/MS and elemental analysis. The properties have been studied by surface tension ( γ CMC ) and conductivity measurements. The thermodynamic parameters of micellization were calculated. The test results show that C 12 -DLADS has lower critical micelle concentration (CMC) and better capability for lowering the γ CMC . The γ CMC and CMC are 36.04 mN/m and 6.03 × 10 −4  mol/L respectively at 45 °C. Moreover, with the increase in temperature, the conductivity of C 12 -DLADS increased, while the counterion binding K 0 decreased. The thermodynamic data show that the micellization process for the surfactant C 12 -DLADS is entropy driven.
ISSN:1097-3958
1558-9293
DOI:10.1007/s11743-012-1349-9