A simple and inexpensive method for producing water-stable pulp fibre yarns using a deep eutectic mixture composed of choline chloride and urea (ChCl/urea) was developed in this work. Deep eutectic solvents (DESs) are eutectic mixtures consisting of two or more components that together have a lower melting point than the individual components. DESs have been previously studied with respect to cellulose dissolution, functionalisation, and pre-treatment. This new method uses a mixture of choline chloride and urea, which is used as a swelling and dispersing agent for the pulp fibres in the yarn-forming process. Although the pulp seemed to form a gel when dispersed in ChCl/urea, the ultrastructure of the pulp was not affected. To enable water stability, pulp fibres were crosslinked by esterification using polyacrylic acid. ChCl/urea could be easily recycled and reused by distillation. The novel process described in this study enables utilisation of pulp fibres in textile production without modification or dissolution and shortening of the textile value chain. An interdisciplinary approach was used, where potential applications were explored simultaneously with material development from process development to the early phase prototyping.
Development of physical properties of bleached eucalyptus kraft pulp is typically based on the refining process. However, many studies have reported that xylan deposition is a viable alternative. As the mechanisms of xylan and cellulose interactions are not clear, the main goal of this study was to achieve a better understanding of these interactions. Considering that a sample of pulp enriched with xylan is a very complex matrix, a model system was developed. Cellulosic thin films were prepared by spincoating and the Langmuir-Schaefer (LS) method from trimethylsilylcellulose (TMSC). Their interactions with xylan were analyzed using the quartz crystal microbalance with dissipation (QCM-D) monitoring technique. The topological changes on cellulose were studied using atomic force microscopy (AFM). For the 13C solid-state nuclear magnetic resonance (NMR) studies, samples were prepared using commercial microcrystalline cellulose (MCC) and xylan. The xylan was extracted from bleached birch kraft pulp using a cold caustic extraction (CCE) method. The QCM-D monitoring showed deposition only with higher concentrations of xylan solution (1 mg · l−1) for the LS method. The AFM images showed that xylan deposits as agglomerates on the cellulose surface, and the NMR experiments showed that there are interactions for the more ordered region of the cellulose fiber and for the less-ordered region.
We report fully-printed top-gate-bottom-contact organic thin-film transistors using substrates prepared from cellulose nanofibers and commercially available printing inks to fabricate the devices. Gravure printing was used to coat the substrate with a polymer resist to decrease the surface roughness and close the surface. Transistor structures were fabricated using inkjet printing for conductors and gravure printing for the dielectric and semiconducting layers. The obtained transistor performance is compared to that of similar transistors on plastic substrate.
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