INRAE, UR BIA, F-44316 Nantes, France.
ICMMP, Université de Poitiers-CNRS, 86000 Poitiers, France.
Biomacromolecules. 2022 Sep 12;23(9):3517-3524. doi: 10.1021/acs.biomac.2c00201. Epub 2022 Aug 31.
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.
纳米纤维素可用于稳定油水表面,形成所谓的 Pickering 乳液。在这项工作中,我们比较了天然和丝光化纤维素纳米晶体(CNC-I 和 CNC-II)在不同 CNC 浓度下吸附在十六烷液滴表面分散在水中的表面组织。这两种类型的 CNC 都具有细长的颗粒形态,并在界面上形成强烈吸附的层。然而,虽然用 CNC-I 形成的层厚与浓度无关,厚度为 7nm,但用 CNC-II 形成的层厚随浓度增加而从 9nm 变化到 14nm,这是通过使用具有匹配对比的小角中子散射实验确定的。分子动力学(MD)模拟表明,两种晶型变体都有一个优先相互作用的结晶平面,暴露了 CH 基团(100 和 010),因此被认为是疏水的。此外,这项研究表明,无论晶型如何,CNC 向油水界面的迁移都是自发和不可逆的,由焓和熵过程驱动。