Cellulose nanocrystals (CNCs) are negatively charged colloidal particles well known to form highly stable surfactant-free Pickering emulsions. These particles can vary in surface charge density depending on their preparation by acid hydrolysis or applying post-treatments. CNCs with three different surface charge densities were prepared corresponding to 0.08, 0.16 and 0.64 e nm −2 , respectively. Posttreatment might also increase the surface charge density. The well-known TEMPO-mediated oxidation substitutes C 6 -hydroxyl groups by C 6 -carboxyl groups on the surface. We report that these different modified CNCs lead to stable oil-in-water emulsions. TEMPO-oxidized CNC might be the basis of further modifications. It is shown that they can, for example, lead to hydrophobic CNCs with a simple method using quaternary ammonium salts that allow producing inverse water-in-oil emulsions. Different from CNC modification before emulsification, modification can be carried out on the droplets after emulsification. This way allows preparing functional capsules according to the layer-by-layer process. As a result, it is demonstrated here the large range of use of these biobased rod-like nanoparticles, extending therefore their potential use to highly sophisticated formulations.
Kraft lignin from black liquor wastes have been converted into epichlorohydrin-crosslinked beads by inverse suspension polymerization. A careful control of the different parameters allowed the preparation of spherical beads with a relatively narrow diameter size distribution. The obtained beads, without permanent porosity, swell well in hydroalcoholic media. Grafting of the sulfonylhydrazine moiety using a two-step route was further performed to apply them to carbonyl compounds scavenging.
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