Abstract

HypothesisThe salinity at which the dynamic phase inversion of the reference system C10E4/n-Octane/Water occurs in the presence of increasing amounts of a test surfactant S2 provides quantitative information on the hydrophilic/lipophilic ratio and on the sensitivity to NaClaq of S2. ExperiencesThe Salinities causing the Phase Inversion (SPI) of the reference system mixed with 12 ionic and 10 nonionic well-defined surfactants are determined in order to quantify the contributions of the nature of the polar head and of the alkyl chain length. FindingsThe SPI varies linearly upon the addition of S2. The slope of the straight variation with the molar fraction of S2 is called the “SPI-slope”. It quantifies the hydrophilic/lipophilic ratio of S2 in saline environment and its salt-sensitivity with respect to the reference surfactant C10E4. The SPI-slopes of C12 surfactants bearing different polar heads are found to decrease in the following order: C12NMe3Br > C12E8 > C12E7 ≥C12SO3Na ≈ C12COONa ≥ C12SO4Na > C12E6 > C12E5 > C12E3. This classification is different from that obtained when the phase inversion is caused by a change in temperature (PIT-slope method) because the addition of NaCl in significant amounts (3 to 10 wt%) partially screens the ionic heads and diminishes their apparent hydrophilicities. A simple model, valid for all types of nonionic surfactants, is developed on the basis of the HLDN equation (Normalized Hydrophilic-Lipophilic Deviation) to express the SPI-slope as a function of the hydrophilic/lipophilic ratio (PACN2) and the salinity coefficient (δ2) of S2. All studied surfactants are positioned on a 2D map according to the values of their SPI-slope and their PIT-slope to graphically highlight their hydrophilic/lipophilic ratio and their salt-sensitivity. Finally, a linear model connecting the PIT-slope and the SPI-slope is derived for nonionics, emphasizing that the thermal partitioning of C10E4 towards n-octane is much greater in the PIT-slope than in the SPI-slope experiments.

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