| Literature DB >> 36044601 |
Somia Haouache1,2, Yu Chen3, Clara Jimenez-Saelices1, Fabrice Cousin4, Pan Chen3, Yoshiharu Nishiyama5, François Jerome2, Isabelle Capron1.
Abstract
Nanocelluloses can be used to stabilize oil-water surfaces, forming so-called Pickering emulsions. In this work, we compare the organization of native and mercerized cellulose nanocrystals (CNC-I and CNC-II) adsorbed on the surface of hexadecane droplets dispersed in water at different CNC concentrations. Both types of CNCs have an elongated particle morphology and form a layer strongly adsorbed at the interface. However, while the layer thickness formed with CNC-I is independent of the concentration at 7 nm, CNC-II forms a layer ranging from 9 to 14 nm thick with increasing concentration, as determined using small-angle neutron scattering with contrast-matched experiments. Molecular dynamics (MD) simulations showed a preferred interacting crystallographic plane for both crystalline allomorphs that exposes the CH groups (100 and 010) and is therefore considered hydrophobic. Furthermore, this study suggests that whatever the allomorph, the migration of CNCs to the oil-water interface is spontaneous and irreversible and is driven by both enthalpic and entropic processes.Entities:
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Year: 2022 PMID: 36044601 PMCID: PMC9472801 DOI: 10.1021/acs.biomac.2c00201
Source DB: PubMed Journal: Biomacromolecules ISSN: 1525-7797 Impact factor: 6.978