ABSTRACT
Several additives, including inorganic (NaCl) and organic salts (derivatives of benzoate), were added into aqueous solutions of a gemini cationic surfactant, 2-hydroxypropyl-1,3-bis (myristyldimethylammonium chloride) (abbreviated as 14-3(OH)-14(2Cl)). The mixed systems were investigated using rheological measurement, cryo-TEM and 1H NMR analysis. The results showed that addition of salts induced rich aggregate morphologies in the 14-3(OH)-14(2Cl)/salt systems. The influence of an inorganic salt on the viscoelasticity of 14-3(OH)-14(2Cl) solutions is much weaker than that of organic salts. Furthermore, the ability of three organic salts in enhancing the viscoelasticity of 14-3(OH)-14(2Cl) solutions is in the order sodium m-hydroxybenzoate > sodium o-hydroxybenzoate > sodium p-hydroxybenzoate. The different roles of these organic salt isomers arise from the different types of hydrogen bonding formed between 14-3(OH)-14(2Cl) and the organic counter ions.
ABSTRACT
A series of unexpected thermo-responsive phenomena were discovered in an aqueous solution of the cationic gemini surfactant, 2-hydroxypropyl-1,3-bis(alkyldimethylammonium chloride) (n-3(OH)-n(2Cl), n = 14, 16), in the presence of an inorganic salt. The viscosity change trend for the 14-3(OH)-14(2Cl) system was investigated in the 20-40 °C temperature range. As the temperature increased, the viscosity of the solution first decreased to a minimum point corresponding to 27 °C, and then increased until a maximum was reached, after which the viscosity decreased again. In the 16-3(OH)-16(2Cl) system, the gelling temperature (T(gel)) and viscosity changes upon heating were similar to those in the 14-3(OH)-14(2Cl) system above 27 °C. The reversible conversion of elastic hydrogel to wormlike micelles in the aqueous solution of the 16-3(OH)-16(2Cl) system in the presence of an inorganic salt was observed at relatively low temperatures. Various techniques were used to study and verify the phase-transition processes in these systems, including rheological measurements, cryogenic transmission electron microscopy (cryo-TEM), electric conductivity, and differential scanning calorimetry. The abovementioned phenomena were explained by the formation and destruction of intermolecular hydrogen bonds, and the transition mechanisms of the aggregates were analyzed accordingly.
ABSTRACT
Aqueous two-phase systems (ATPS) were obtained in the aqueous mixtures of a cationic surfactant and a series of ionic liquids (ILs). The effects of IL structure, temperature and additives on the phase separation were systematically investigated. The microstructures of some ATPS were observed by freeze-fracture replication technique. Lyotropic liquid crystal was found in the bottom phase besides micelles under different conditions. Remarkably, both IL structure and additives profoundly affected the formation and properties of the ATPSs. The phase separation can be attributed to the existence of different aggregates and the cation-π interactions of the cationic surfactant with the ILs, which has a significant role in the formation of ATPS. The extraction capacity of the studied ATPS was also evaluated through their application in the extraction of two biosubstances. The results indicate that the ILs with BF4(-) as anion show much better extraction efficiencies than the corresponding ILs with Br(-) as anion do under the same conditions. l-Tryptophan was mainly distributed into the NPTAB-rich phase, while methylene blue and capsochrome were mainly in the IL-rich phase.
