Analysis of the Porous Architecture and Properties of Anisotropic Nanocellulose Foams: A Novel Approach to Assess the Quality of Cellulose Nanofibrils (CNFs)

Cellulose nanofibrils (CNFs) are a unique nanomaterial because of their abundant, renewable, and biocompatible origin. Compared with synthetic nanoparticles, CNFs are commonly produced from cellulose fibers (e.g., wood pulp) by repetitive high-shear mechanical disintegration. Yet, this process is still highly demanding in energy and costly, slowing down the large-scale production and commercialization of CNFs. Reducing the energy consumption during fibers fibrillation without using any chemical or enzymatic pretreatments while sustaining the CNF quality is challenging. Here, we show that the anisotropic properties of the CNF foams are directly connected to the degree of nanofibrillation of the cellulose fibers. CNFs were produced from wood pulps using a grinder at increasing specific energy consumptions. The anisotropic CNF foams were made by directional ice templating. The porous architecture, the compressive behavior of the foams, and the CNF alignment in the foam cell walls were correlated to the degree of fibrillation. A particular value of specific energy consumption was identified with respect to the highest obtained foam properties and CNF alignment. This value indicated that the optimal degree of fibrillation, and thus CNF quality, was achieved for the studied cellulose pulp. Our approach is a straightforward tool to evaluate the CNF quality and a promising method for the benchmarking of different CNF grades

Shape-Anisotropic Polyimide Particles by Solid-State Polycondensation of Monomer Salt Single Crystals

Shape-anisotropic particles are of broad interest, e.g., for colloidal crystals or applications at interfaces such as particle-stabilized emulsions. Despite the wealth of accessible shapes of inorganic particles, anisotropic homopolymer particles are to date mostly limited to objects derived from spheres (e.g., ellipsoidal or disk-shaped particles). Here, we report the synthesis of shape-anisotropic, angular polyimide particles by thermal solid-state polycondensation (SSP) of monomer salts. We prepare monomer salt single crystals of relatively narrow size and shape distribution by growth inside hydrogels, and solve their crystal structure. Polyimide particles are obtained by simple heating and retain the shape of the initial salt crystals. Using high-temperature X-ray diffraction, thermal analyses and microscopy techniques, we investigate the mechanism of the transformation. The obtained polyimide particles are temperature-stable up to 640 °C and virtually insoluble in any solvent. This work sheds more light on the mechanism of SSP of monomer salts and reports a new methodology for accessing nonspherical homopolymer particles, which are due to their outstanding stability potentially of interest for applications under extreme conditions