Loading…
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...
Saved in:
Published in: | Journal of surfactants and detergents 2012-11, Vol.15 (6), p.703-707 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
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 |