University Grenoble Alpes, CNRS, Grenoble INP (Institute of Engineering ), LGP2, F-38000 Grenoble, France.
Department of Bioproducts and Biosystems, School of Chemical Engineering, Aalto University, P.O. Box 16300, Aalto, Espoo FIN-00076, Finland.
Biomacromolecules. 2021 Feb 8;22(2):880-889. doi: 10.1021/acs.biomac.0c01596. Epub 2020 Dec 30.
Cellulose (CNF) and chitin (ChNF) nanofibers are known to form materials that are both tough and strong. In this study, we hypothesize that the inertness of networks produced from CNF and ChNF makes them ideal templates for heterogeneous reactions and formation of nanoarchitectures. We expand nanoparticle templating on polysaccharide colloids by introducing a new and facile process that leads to the growth of organic nanoparticles on CNF and ChNF in aqueous media. The process, based on solvent shifting supported on solid interfaces, is demonstrated by direct observation of lignin nanoparticles that are further used for their photocatalytic activity. Importantly, the dynamics of nanoparticle nucleation and growth is correlated with the surface chemistry of the templating nanopolysaccharides. Electrostatic repulsion between the deprotonated lignin molecules and the slightly negative CNF support led to limited adsorption and was effective in producing free (nonbound) lignin nanoparticles (28 ± 7 nm) precipitation. In contrast, the stronger interfacial interactions between the positively charged ChNF and lignin molecules facilitated instantaneous and extensive lignin adsorption, followed by nucleation and growth into relatively larger nanoparticles (46 ± 17 nm). The latter were homogeneously distributed and strongly coupled to the ChNF support. Overall, we introduce lignin nanoparticle nucleation and growth on renewable nanopolysaccharides, offering an effective route toward synthesis of highly functional fibrils and related cohesive films that offer a great potential in packaging and other applications.
纤维素 (CNF) 和几丁质 (ChNF) 纳米纤维以形成既坚韧又坚固的材料而闻名。在这项研究中,我们假设 CNF 和 ChNF 形成的网络的惰性使它们成为异相反应和纳米结构形成的理想模板。我们通过引入一种新的简便工艺扩展了多糖胶体上的纳米颗粒模板化,该工艺导致在水介质中 CNF 和 ChNF 上有机纳米颗粒的生长。该工艺基于在固体界面上支持的溶剂转移,通过直接观察木质素纳米颗粒得到证明,进一步利用其光催化活性。重要的是,纳米颗粒成核和生长的动力学与模板纳米多糖的表面化学有关。木质素分子的去质子化与 CNF 支撑物的轻微负电荷之间的静电排斥导致有限的吸附,有效地产生了游离(未结合)木质素纳米颗粒(28 ± 7nm)沉淀。相比之下,带正电荷的 ChNF 和木质素分子之间更强的界面相互作用促进了木质素的瞬时和广泛吸附,随后进行成核和生长成相对较大的纳米颗粒(46 ± 17nm)。后者均匀分布且与 ChNF 支撑物紧密结合。总的来说,我们在可再生纳米多糖上引入了木质素纳米颗粒的成核和生长,为合成具有高功能的原纤维和相关的有凝聚力的薄膜提供了有效途径,这些纤维和薄膜在包装和其他应用中具有巨大的潜力。