Abstract:We have prepared a series of novel gemini surfactants having ester bonds in their structures. These surfactants possess two identical hydrophilic polyethylene glycol moieties, two hydrophobic alkyl group moieties, and an anionic spacer. The structures of these compounds were confirmed through infrared and nuclear magnetic resonance spectroscopic and elemental analyses. The novel gemini surfactants exhibit excellent surface activity in terms of their surface tension, low-foaming, wetting power, and fluorescence… Show more
“…Besides, they have better wetting, solubilizing and foaming properties, and good mildness to the skin, safe ecology, and environmental control [5,6]. These unique properties make them potentially useful in many applications, for example, in soil remediation, enhanced oil recovery, drug entrapment and release, and the construction of high-porosity materials [7][8][9][10].…”
A straightforward synthetic strategy to an anionic gemini surfactant having both N‐acylamide and carboxylate groups in a molecule has been demonstrated. The surface properties of the anionic gemini surfactant, such as CMC (critical micelle concentration), C20 (the concentration required to reduce the surface tension of the solvent by 20 mN/m), γCMC (the surface tension at the CMC), ∏CMC (the surface pressure at the CMC), Γmax (the maximum surface excess concentration at the air/aqueous solution interface), Amin (the minimum area per surfactant molecule at the air/water interface), and the CMC/C20 ratio (a measure of the tendency to form micelles relative to adsorbtion at the air/water interface), have been studied. The influence of the different concentrations of NaCl on the surface properties of the gemini surfactant has been discussed. The results have shown that the CMC values decreased with an increase in the concentration of NaCl indicating that the Na+ preferentially adsorbs onto the surface of the charged aggregate and facilitates the aggregate growth by suppressing the main impediment of electrostatic repulsion among head groups. Additionally, the values of Γmax are always higher in salt solutions as compared to those in pure water due to their salting out effect. The larger pC20 value indicates that the surfactant adsorbs more efficiently at the air/water interface and reduces surface tension more efficiently. In addition, the geminis in water show little or no break in their specific conductance versus surfactant molar concentration plots. This is attributable to protonation of the carboxylate group and strong Na+ release during micellization.
“…Besides, they have better wetting, solubilizing and foaming properties, and good mildness to the skin, safe ecology, and environmental control [5,6]. These unique properties make them potentially useful in many applications, for example, in soil remediation, enhanced oil recovery, drug entrapment and release, and the construction of high-porosity materials [7][8][9][10].…”
A straightforward synthetic strategy to an anionic gemini surfactant having both N‐acylamide and carboxylate groups in a molecule has been demonstrated. The surface properties of the anionic gemini surfactant, such as CMC (critical micelle concentration), C20 (the concentration required to reduce the surface tension of the solvent by 20 mN/m), γCMC (the surface tension at the CMC), ∏CMC (the surface pressure at the CMC), Γmax (the maximum surface excess concentration at the air/aqueous solution interface), Amin (the minimum area per surfactant molecule at the air/water interface), and the CMC/C20 ratio (a measure of the tendency to form micelles relative to adsorbtion at the air/water interface), have been studied. The influence of the different concentrations of NaCl on the surface properties of the gemini surfactant has been discussed. The results have shown that the CMC values decreased with an increase in the concentration of NaCl indicating that the Na+ preferentially adsorbs onto the surface of the charged aggregate and facilitates the aggregate growth by suppressing the main impediment of electrostatic repulsion among head groups. Additionally, the values of Γmax are always higher in salt solutions as compared to those in pure water due to their salting out effect. The larger pC20 value indicates that the surfactant adsorbs more efficiently at the air/water interface and reduces surface tension more efficiently. In addition, the geminis in water show little or no break in their specific conductance versus surfactant molar concentration plots. This is attributable to protonation of the carboxylate group and strong Na+ release during micellization.
“…Cationic 14-E2-14 was found to undergo chemical hydrolysis in alkaline condition and thus was cleaved through chemical means by using phosphatebuffered saline and sodium hydroxide/potassium hydrogen phosphate (Ringer Buffer) [21].…”
Section: Cleavable Propertiesmentioning
confidence: 99%
“…Cleavable/biodegradable gemini surfactants are the better alternatives. With this view point, a number of surfactants with polar or labile bonds (amide, carbonate, ethoxylated, fluorinated and ester containing) which are highly soluble, easily hydrolysable, less stable and degradable, have, therefore, been synthesized by many workers [17][18][19][20][21]. As the nature of spacer and the constituent groups play a significant role in the micellization process of the gemini surfactants, the abovementioned surfactants show interesting properties.…”
A novel anionic Gemini surfactant containing oxygen atoms in the linking group was designed and synthesized. The surface properties of the anionic Gemini surfactant were investigated by measuring the surface tension and conductivity. The Gemini surfactant showed a low critical micelle concentration value, which decreases with increasing concentration of NaCl. The calculated physicochemical properties indicate that oxygen atoms in the linking group interact with water molecules stronger than CH2.
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