Adsorption at the biocompatible α-pinene–water interface and emulsifying properties of two eco-friendly surfactants

• Published in: Colloids and surfaces, B, Biointerfaces B, Biointerfaces, 2014-10, Vol.122, p.623-629
• Main Authors: Trujillo-Cayado, Luis Alfonso, Ramírez, Pablo, Alfaro, María Carmen, Ruíz, Manuela, Muñoz, José
• Format: Article
• Language: English
• Subjects: Adsorption; Adsorption equilibrium; Biocompatible Materials; Droplets; Eco-friendly surfactant; Emulsification; Emulsions; Esters; Glycerols; Interfacial pressure isotherm; Monoterpenes - chemistry; Rheology; Surface chemistry; Surface rheology; Surface Tension; Surface-Active Agents - chemistry; Surfactants; Water - chemistry; α-Pinene
• ISSN: 0927-7765; 1873-4367
• DOI: 10.1016/j.colsurfb.2014.07.041

•A model assuming the coexistence of different adsorbed states was used.•Levenol C201 showed higher compressibility and molecular interaction than H&B.•Both surfactants are partly solubilized in α-pinene.•These surfactants produced concentrated emulsions with α-pinene as oil phase.•The most stable emulsion was the one prepared with Levenol C201. In this contribution, we provide an accurate characterization at the α-pinene/water interface of two commercial polyoxytheylene glycerol ester surfactants which differ in the number of ethylene oxide (EO) groups, comprising a systematic analysis of interfacial pressure isotherms, dynamic curves, interfacial rheology and emulsifying properties. Polyoxyethylene glycerol esters derived from cocoa oil are non-ionic surfactants obtained from a renewable source which fulfill the environmental and toxicological requirements to be used as eco-friendly emulsifying agents. α-Pinene is a renewable biosolvent completely insoluble in water, which could find numerous applications. Interfacial rheology and equilibrium interfacial pressure data fitted a rigorous reorientation model that assumes that the surfactant molecules, when adsorbed at the interface, can acquire two orientations. The surfactant with the highest number of EO groups (Levenol C201) turned out to be more surface active at the α-pinene/water interface. In addition, the surfactant with the lowest number of EO groups (Levenol H&B) is solubilized into the adjacent oil phase. Slightly concentrated α-pinene emulsions were obtained using both surfactants. Nevertheless, more stable α-pinene emulsions with smaller droplet sizes and lower polidispersity were obtained when Levenol C201 was used as emulsifier instead of Levenol H&B. The systematic characterization presented in this work provides important new findings on the interfacial and emulsifying properties of polyoxytheylene glycerol ester surfactants, which can be applied in the rational development of new biocompatible products.