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Abstract In the last years, hydrogels from renewable biopolymers and low-cost row materials are a hot topic for biomedical applications. In this context, cellulose nanofibrils are considered suitable building blocks for the synthesis of many biocompatible products, with a variety of chemical-physical properties. Herein we report a multi-technique and multi-scale study, from the molecular to the nanometric length scale, of the sol–gel transition observed in aqueous solutions of TEMPO-oxidized nano-sized cellulose fibrils (TOCNFs), when in the presence of polyvalent cations (Mg2+ and Ca2+). We combine the data from Small Angle Neutron Scattering (SANS), which provide information about the inner structure of the nanofibril, with those from UV Resonant Raman (UVRR) spectroscopy, which is a sensitive probe of the intra- and inter-molecular interactions in the gel and the liquid state. The transition between the gel and the liquid phases is investigated as a function of the concentration of both TOCNFs and cations, the nature of the latter, and the pH at which the phenomenon is observed. SANS analysis reveals that ion concentration induces an anisotropic swelling in the nanofibrils which, at the same time, become more and more flexible. The nanofibrils flexibility is also dependent on TOCNF concentration and pH value. UVRR allows us to elucidate the structural organization and hydrogen-bonding properties of water in aqueous TOCNF dispersions and gels, showing how water molecules partially lose their typical bulk-like tetrahedral organization when ions are added, and the gel phase is formed. Graphical abstract

Cellulose nano-sponges (CNS), obtained by cross-linking TEMPO oxidized and ultra-sonicated cellulose nano-fibers (TOUS-CNFs) with branched polyethyleneimine (bPEI), underwent here a systematic small angle neutron scattering investigation, by varying the amount of cross-linker and the water content. The aim was to provide experimental evidence of nano-porosity in the TOUS-CNF network of these nano-sponges (CNSs) by investigating the water nano-confinement geometries in the adsorbent material. Moreover, we also verified how the breaking/reformation of specific intermolecular hydrogen bond interactions between water and the chemical groups present in the architecture of the CNSs could contribute to regulate the water adsorption process observed at macroscopic level. The analysis of the experimental data, performed in terms of the correlation length model, allowed us to extract the short-range correlation length ξ, interpreted as a very first indirect estimation of the effective nano-dimension of the cavities produced by the cross-linking of the reticulated cellulose nano-fibers. From the model, power-law (n) and Lorentzian (m) exponents have been also obtained, associated with the density of TOUS-CNFs at high (larger than hundreds of A) and low (~ 10–100 A) spatial scales, respectively. These parameters were all sensitive to the structural variations induced by the progressive uptake of water on the bPEI/TOUS-CNF sponges with different bPEI:TOUS-CNF (w/w) ratios. Finally, we investigated the effect of the addition of citric acid in the CNS formulation, confirming its role in increasing cross-linking density and sponge rigidity. The obtained results appear crucial in order to rationalize the design of these sponges and to track the changes in the ability of the final products as efficient nano-confinement systems for water.

Co-author Andrea Fiorati’s status as one of the two corresponding authors was not originally indicated on the published version. This Correction remedies that omission.