4.7 Article

Surface, interfacial and thermodynamic aspects of the Rhamnolipid-salt systems

Journal

JOURNAL OF MOLECULAR LIQUIDS
Volume 384, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.molliq.2023.122245

Keywords

Rhamnolipid-salt system; Critical micelle concentration; Surface tension; Surface excess; Adsorption and micellization; Contact angle

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This study investigated the variations in thermodynamic and physicochemical properties of the rhamnolipid-salt system. The results showed that the addition of salts significantly reduced the critical micelle concentration (CMC) and surface tension of rhamnolipids, leading to changes in wettability and the formation of agglomerated structures.
Rhamnolipids have been exploited for fluid-fluid and solid-fluid interactions in various applications due to their excellent surface and interfacial properties. The present work deals with the rhamnolipid-salt system and measured the variation in the thermodynamic and physicochemical properties. A systemic investigation has been carried out; first measured the critical micelle concentration (CMC) of rhamnolipid (200 mg/L) and then the effect of salts over various physiochemical properties of biosurfactant was evaluated. Further, the concentration of rhamnolipid was varied with the selected salts (NaCl, Na2CO3, NaNO3) at optimum concentrations. The physio-chemical characterization of biosurfactant-salt systems was conducted by performing surface tension, particle size/zeta potential, contact angle and microscopic analyses using a tensiometer, dynamic light scat-tering, goniometer and microscope, respectively. The results demonstrated that the CMC values of rhamnolipid in the biosurfactant-salts system were reduced to 40-60 mg/L. The addition of electrolyte in the rhamnolipid reduced the CMC and surface tension values significantly, which altered the wettability and formed agglomer-ated structure. The contact angle of rhamnolipid decreased from 76 & DEG; to 58 & DEG; in the presence of salt. The reductions in surface tension and CMC value of rhamnolipid have been correlated with the physio-chemical properties of biosurfactant-salt systems. Further, Gibb's standard free surface energies of rhamnolipid micellization and adsorption at the air-water interface were estimated to predict the thermodynamical behaviour. At CMC values, the surface excess of rhamnolipid was 2.09 x 10-6 mol/m2, which reduced to 1.93 x 10-6 mol/m2 for rhamnolipid-salt systems.

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