Department of Chemistry, Institute of Chemistry for Renewable Resources, University of Natural Resources and Life Sciences Vienna (BOKU), Konrad-Lorenz-Straße 24, A-3430 Tulln, Austria.
Nanoscale. 2019 Oct 3;11(38):17773-17781. doi: 10.1039/c9nr05309c.
High axial aspect crystalline nanomaterials have emerged as polymeric building blocks for the construction of supermaterials. In contrast to this form, amorphous nanospheres have remained largely untapped. This is especially peculiar in the context of material assembly, due to the wide range of opportunities they offer by virtue of their soft particle characteristics, high volume ratio at low solid content and their highly swollen and accessible structure. In the context of cellulose, these colloids represent a new field in the family of nanocelluloses. We report an organic solvent-free, heterogeneous and simple synthesis of spherical carboxylated nanoparticles bearing a distinctive, amorphous outer shell structure. The particle shape is evaluated by atomic force microscopy, cryo-transmission electron microscopy, dynamic light scattering and small-angle X-ray scattering. The soft shell structure of the particles and their responsiveness to ionic strength and pH are quantified by the combination of quartz-crystal microgravimetry and atomic force microscopy. Aqueous dispersions of the nanocolloids feature distinctive sol/gel behaviour: at solid content <2 wt% they behave as a low viscous liquid (sol state), whereas at higher concentrations the shells dominate the interparticle interactions, causing an exponential increase in viscosity, typical of a gel state (hydrogel). Gelation is reversible and can be triggered alternatively by protonation of the carboxylate groups under acidic conditions. Supercritical drying of the hydrogels yields a highly porous, isotropic aerogel composed of aggregated nanoparticles. In contrast, ambient drying results in an anisotropic, fully transparent film. These colloids will allow the study of the interaction between soft cellulose and rigid matter, and have high potential as toughening additives in composites. Furthermore, the amorphous nature of this new class of cellulose nanocolloids makes them attractive as support materials for catalysts and enzymes.
高轴向比的结晶纳米材料已成为构建超材料的聚合结构单元。相比之下,非晶态纳米球在很大程度上尚未得到开发。这在材料组装的背景下尤为特殊,因为它们具有软颗粒的特性,在低固体含量下具有高体积比,以及高度溶胀和可及的结构,从而提供了广泛的机会。在纤维素的背景下,这些胶体代表了纳米纤维素家族中的一个新领域。我们报告了一种无有机溶剂、多相且简单的方法,用于合成具有独特非晶外壳结构的球形羧基化纳米颗粒。通过原子力显微镜、低温传输电子显微镜、动态光散射和小角 X 射线散射评估颗粒形状。通过石英晶体微天平与原子力显微镜相结合,定量研究了颗粒的软壳结构及其对离子强度和 pH 的响应。纳米胶体的水性分散体具有独特的溶胶/凝胶行为:在固体含量 <2wt%时,它们表现为低粘性液体(溶胶状态),而在更高浓度下,壳层主导着颗粒间的相互作用,导致粘度呈指数增长,表现出凝胶状态(水凝胶)的典型特征。凝胶化是可逆的,可以通过在酸性条件下质子化羧酸盐基团来触发。水凝胶的超临界干燥得到由聚集纳米颗粒组成的高度多孔、各向同性的气凝胶。相比之下,环境干燥会导致各向异性、完全透明的薄膜。这些胶体将允许研究软纤维素与刚性物质之间的相互作用,并在复合材料中作为增韧添加剂具有很高的潜力。此外,这种新型纤维素纳米胶体的非晶态性质使其成为催化剂和酶的支撑材料的理想选择。