“…sulfate (anionic, SDS), ,,,, carboxylate (anionic, e.g. sodium cholate), , benzyl sulfonate (anionic, dodecyl benzyl sulfonate), , imidazolium (cationic, 1-decyl-3-methylimidazolium chloride), trialkyl-ammonium (cationic, e.g., cetyltrimethylammonium bromide). , These studies infer that an attractive interaction between HPC and ionic-surfactant increases its cloud point temperature, solution viscosification, reduced counterion binding, and overall negative enthalpy change. , On the other hand, an increase in surfactant tail-length (or number of carbon atoms, n c ) enhances PS stability, growth rate, and HPC-surfactant binding cooperativity. ,,, All these results collectively propose that during PS formation charge–dipole interaction play a dominant role; however, short-range hydrophobic forces also play a meaningful role in the overall free energy change. Moreover, earlier studies ,,, have revealed that anionic surfactants, specifically those having sulfate headgroup, make a stronger interaction with HPC than the cationic ones.…”