Foam-formed cellulose biocomposites are a promising technology for developing lightweight and sustainable packaging materials. In this work, we produce and characterize biocomposite foams based on methylcellulose (MC), cellulose fibers (CF), and lignin (LN). The results indicate that adding organosolv lignin to a foam prepared using MC and CF moderately increases Young’s modulus, protects the foam from the growth of Escherichia coli bacteria, and improves the hydrophobicity of the foam surface. This article concludes that organosolv lignin enhances many properties of cellulose biocomposite foams that are required in applications such as insulation, packaging, and cushioning. The optimization of the foam composition offers research directions toward the upscaling of the material solution to the industrial scale. Graphical

Colloidal gels are soft solids composed of particles dispersed in a fluid phase. Their rheological behavior highly depends on the particle concentration, but establishing a relationship can be challenging. This article showcases the potential of fractional rheology to model and predict linear viscoelastic responses of colloidal hydrogels containing TEMPO-oxidized cellulose nanofibers. Cellulose nanofiber hydrogels are soft solids whose rheology is directly related to the particle concentration. Therefore, this work defined the rheological behavior of the hydrogels using a fractional order derivative analytically solved to determine rheological responses in frequency, stress relaxation, and creep. Using two parameters, it evaluated the rheology of cellulose nanofiber hydrogels and established tests that predict rheological behaviors for given particle concentrations. The findings suggested that the fractional approach could become a standard method for characterizing cellulose nanofiber hydrogels in the reported concentration regime. The two parameters of the fractional model build a comparison framework to assess the rheology of different viscoelastic materials. Graphic

This work reports the dielectric behavior of the biopolymer ethyl cellulose (EC) observed from transient currents experiments under the action of a direct current (DC) electric field (~10⁷ V/m) under vacuum conditions. The viscoelastic response of the EC was evaluated using dynamic mechanical analysis (DMA), observing a mechanical relaxation related to glass transition of around ~402 K. Furthermore, we propose a mathematical framework that describes the transient current in EC using a fractional differential equation, whose solution involves the Mittag–Leffler function. The fractional order, between 0 and 1, is related to the energy dissipation rate and the molecular mobility of the polymer. Subsequently, the conduction mechanisms are considered, on the one hand, the phenomena that occur through the polymer–electrode interface and, on the other hand, those which manifest themselves in the bulk material. Finally, alternating current (AC) conductivity measurements above the glass transition temperature (~402 K) and in a frequency domain from 20 Hz to 2 MHz were carried out, observing electrical conduction described by the segmental movements of the polymeric chains. Its electrical properties also position EC as a potential candidate for electrical, electronics, and mechatronics applications.