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Abstract: There is a need to develop high‐performance cellulose fibers as sustainable replacements for glass fibers, and as alternative precursors for carbon filaments. Traditional fiber spinning uses toxic solvents, but in this study, by using dimethyl sulfoxide (DMSO) as a co‐solvent with an ionic liquid, a novel high‐performance fiber with exceptional mechanical properties is produced. This involves a one‐step dissolution, and cost‐effective route to convert high concentrations of low molecular weight microcrystalline cellulose into high stiffness cellulose fibers. As the cellulose concentration increases from 20.8 to 23.6 wt%, strong optically anisotropic patterns appear for cellulose solutions, and the clearing temperature (Tc) increases from ≈100 °C to above 105 °C. Highly aligned, stiff cellulose fibers are dry‐jet wet spun from 20.8 and 23.6 wt% cellulose/1‐ethyl‐3‐methylimidazolium diethyl phosphate/DMSO solutions, with a Young's modulus of up to ≈41 GPa. The significant alignment of cellulose chains along the fiber axis is confirmed by scanning electron microscopy, wide‐angle X‐ray diffraction, and powder X‐ray diffraction. This process presents a new route to convert high concentrations of low molecular weight cellulose into high stiffness fibers, while significantly reducing the processing time and cost. [ABSTRACT FROM AUTHOR]

A deep eutectic solvent composed of choline chloride (ChCl) and urea has been recently introduced as a promising cellulose compatible medium that enables e.g. fibre spinning. This paper clarifies the influence of such a solvent system on the structure and chemical composition of the cellulosic pulp fibres. Special emphasis was placed on the probable alterations of the chemical composition due to the dissolution of the fibre components and/or due to the chemical derivatisation taking place during the DES treatment. Possible changes in fibre morphology were studied with atomic force microscopy and scanning electron microscopy. Chemical compositions of pulp fibres were determined from the carbohydrate content, and by analysing the elemental content. Detailed structural characterisation of the fibres was carried out using spectroscopic methods; namely X-Ray Photoelectron Spectroscopy, solid state Nuclear Magnetic Resonance and Raman Spectroscopy. No changes with respect to fibre morphology were revealed and negligible changes in the carbohydrate composition were noted. The most significant change was related to the nitrogen content of the pulp after the DES treatment. Comprehensive examination using spectroscopic methods revealed that the nitrogen originated from strongly bound ChCl residuals that could not be removed with a mild ethanol washing procedure. According to Raman spectroscopic data and methylene blue adsorption tests, the cationic groups of ChCl seems to be attached to the anionic groups of pulp by electrostatic forces. These findings will facilitate the efficient utilisation of DES as a cellulose compatible medium without significantly affecting the native fibre structure. [ABSTRACT FROM AUTHOR]

We report the production of cellulose-derived hybrid carbon nanofiber (CNF)/carbon nanotubes (CNTs) electrodes for the fabrication of high-performance supercapacitors. The CNTs were grown via a floating catalyst chemical vapor deposition (CVD) method on the top surface of electrospun cellulose-derived CNFs. The morphology of these hybrid CNF/CNTs fibrous structures was investigated using scanning electron and transmission electron microscopy. The development of these carbon structures was characterized using Raman spectroscopy. The electrochemical performance of the devices including cyclic voltammetry (CV), galvanostatic charge/discharge (GCD), electrochemical impedance spectroscopy measurements (EIS), and electrochemically stability was carried out. These hybrid CNF/CNTs electrodes had a high value of specific capacitance of 149 F g-1 at a current density 0.5 A g-1, an increase of 15% compared with pristine CNFs. The BET specific surface area increases from 712 m² g-1 to 1211 m² g-1 from pristine CNFs to hybrid CNF/CNTs, leading to a specific capacitance (per unit area) of ~170 mF cm-2. These supercapacitors also retain 90% of the original capacitance over 1000 cycles, showing an excellent stability. This method of supercapacitor electrode production is suggested as a basis to convert a sustainable cellulosic material into a useful energy storage material. [ABSTRACT FROM AUTHOR]

Microfibrillated cellulose (MFC) obtained from eucalyptus was embedded in gelatin from two sources; namely bovine and salmon gelatin. Raman spectroscopy revealed that stress is transferred more efficiently from bovine gelatin to the MFC when compared to salmon gelatin. Young’s modulus, tensile strength, strain at failure and work of fracture of the nanocomposite films were improved by ∼67, 131, 43 y 243% respectively when using salmon gelatin as matrix material instead of bovine gelatin. Imaging of the tensile fracture surface of the MFC-gelatin nanocomposites revealed that crack formation occurs predominantly within bovine and salmon gelatin matrices rather than within the MFC or at the MFC/gelatin interface. This suggests that the mechanical failure mechanism in these nanocomposite materials is predominantly governed by a matrix-cohesive fracture mechanism. Both strength and flexibility are desirable properties for composite coatings made from gelatin-based materials, and so the findings of this study could assist in their utilization in the food and pharmaceutical industry. [ABSTRACT FROM AUTHOR]

The molecular deformation and crystal orientation of a range of next generation regenerated cellulose fibers, produced from an ionic liquid solvent spinning system, are correlated with macroscopic fiber properties. Fibers are drawn at the spinning stage to increase both molecular and crystal orientation in order to achieve a high tensile strength and Young’s modulus for potential use in engineering applications. Raman spectroscopy was utilized to quantify both molecular strain and orientation of fibers deformed in tension. X-ray diffraction was used to characterize crystal orientation of single fibers. These techniques are shown to provide complimentary information on the microstructure of the fibers. A shift in the position of a characteristic Raman band, initially located at ∼1095 cm −1 , emanating from the backbone structure of the cellulose polymer chains was followed under tensile deformation. It is shown that the shift rate of this band with respect to strain increases with the draw ratio of the fibers, indicative of an increase in the axial molecular alignment and subsequent deformation of the cellulose chains. A linear relationship between the Raman band shift rate and the modulus was established, indicating that the fibers possess a series aggregate structure of aligned crystalline and amorphous domains. Wide-angle X-ray diffraction data show that crystal orientation increases with an increase in the draw ratio, and a crystalline chain slip model was used to fit the change in orientation with fiber draw ratio. In addition to this a new model is proposed for a series aggregate structure that takes into better account the molecular deformation of the fibers. Using this model a prediction for the crystal modulus of a cellulose-II structure is made (83 GPa) which is shown to be in good agreement with other experimental approaches for its determination. [ABSTRACT FROM AUTHOR]

The textile industry is resource-intensive, which has a significant impact on global emissions and waste pollution. To meet the demand of textiles over a third of fibres used in manufacturing are sourced from fossil fuels. As the global demand for textiles continues to grow, manufacturers are having to seek innovative approaches to providing sustainable and regenerative cellulose fibres. However, the latest climate change pressures on the textile industry have uncovered grave environmental issues associated with traditional regenerative cellulose production, such as the viscose manufacturing process. The viscose process requires intensive use of hazardous chemicals which leads to water pollution and ecotoxicity. In addition, if forestry products are unsustainably sourced for this process, this can lead to resource scarcity and deforestation. To provide a holistic solution for mitigating these challenges this study uses the by-products of paper manufacturing dissolved in an ionic liquid to produce regenerated cellulose filaments. Paper mill sludge (PMS) is a cellulosic by-product typically used on animal bedding and land spreading. The material has been dissolved in an ionic liquid - 1-ethyl-3-methylimidazolium diethyl phosphate - with the aid of a co-solvent dimethyl sulfoxide (DMSO) - and spun into continuous filaments for textile production. The mechanical properties of paper sludge filaments are found to be competitive with commercial viscose, which is promising for their drop-in replacement. It is also demonstrated that by increasing the concentration of the PMS from 9% to 12.4%, an improvement of the filament properties can be achieved; an increase in modulus from ∼19 GPa to ∼26 GPa and strength from ∼223 MPa to ∼282 MPa. These values are shown to be competitive with other commercial, less sustainable, regenerated cellulose fibres. Image 1 [ABSTRACT FROM AUTHOR]