RESUMEN

Nanocellulose is a well-known stabilizer for several colloidal dispersions, including emulsions and solid nanoparticles, replacing surfactants, polymers, and other additives, and therefore providing more minimalistic and eco-friendly formulations. However, could this ability be extended to stabilize oil droplets and inorganic nanoparticles simultaneously in the same colloidal system? This work aimed to answer this question. We evaluated both cationic and anionic nanofibrillated celluloses to stabilize both titanium dioxide nanoparticles and oil droplets. The resulting suspensions held their macroscopic stability for up to 2 months, regardless of pH or surface charge. Cryo-TEM images revealed a complex network formation involving nanofibers and TiO2 nanoparticles, which agrees with the high viscosity values and gel-like behavior found in rheology measurements. We propose that the formation of this network is responsible for the simultaneous stabilization of oil droplets and TiO2 nanoparticles, and that this may be used as a formulation tool for other complex systems.

Asunto(s)

Celulosa , Nanopartículas , Titanio , Emulsiones

RESUMEN

HYPOTHESIS: Hydrophobic oleic acid/water interfaces are negatively charged. Hence, the use of cationic nanocelluloses as stabilizers of Pickering emulsions could improve the colloidal stability due to the electrostatic complexation at the oil-water interface. EXPERIMENTS: Two cationic nanofibrillated cellulose (cNFCs) with two degrees of substitution were prepared and used as stabilizers of Pickering emulsions. The adsorption of cNFCs at the oil: water interface was evaluated by interfacial tension, atomic force microscopy, and centrifugation measurements. LUMiSizer and optical microscopy techniques were used to analyze the colloidal stability and oil droplets morphology, respectively. Besides, the rheological behavior of the continuous aqueous phase was determined through flow and stress sweep curves. Finally, the dispersion of cNFCs in a diluted emulsion was visualized by cryogenic transmission electron microscopy (cryo-TEM). FINDINGS: Cationic NFCs were more efficient in partitioning to the oil:water interface compared to their anionic analogous, oCNF. The electrostatic attraction between the positively charged trimethylammonium groups and the negatively charged deprotonated oleic acid reduced the interfacial tension and improved the colloidal stability of O/W Pickering emulsions. cNFCs dispersed in the aqueous phase were found to increase the viscosity, decelerating the oil drops coalescence. Therefore, the stabilization of cNFCs Pickering emulsions had a synergistic effect from the electrostatic complexation at the liquid-liquid interface and network formation in the aqueous phase, as visualized by cryo-TEM.