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Cotton fiber is favored by people because of its good moisture absorption, heat preservation, soft feel, comfortable wearing and other excellent performance. In recent years, due to the destruction of the ozone layer, the intensity of ultraviolet radiation at ground level has increased. Cotton fiber will degrade under long time ultraviolet irradiation, which limits the outdoor application of cotton fiber. In this study, titanium dioxide (TiO2) particles were prepared on the surface of cotton fibers with the help of supercritical carbon dioxide (SCCO2) to improve the UV resistance of cotton fibers. The effects of SCCO2 treatment on the morphology, surface composition, thermal stability, photostability and mechanical properties of TiO2 were studied by Fourier transform infrared spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, thermogravimetric analysis, UV-VIS spectroscopy, and single fiber test. The results showed that TiO2 particles were generated on the fiber surface, which reduced the photo-degradation rate of cotton fiber. This is because TiO2 can absorb UV rays and reduce the absorption of UV rays by the cotton fiber itself. The synthesis process of SCCO2 is simple and environmentally friendly, which provides a promising technology for the synthesis of metal nitrogen dioxide on natural plant fibers. [ABSTRACT FROM AUTHOR]

The development of green materials, especially the preparation of high-performance conductive hydrogels from biodegradable biomass materials, is of great importance and has received worldwide attention. As an aromatic polymer found in many natural biomass resources, lignin has the advantage of being renewable, biodegradable, non-toxic, widely available, and inexpensive. The unique physicochemical properties of lignin, such as the presence of hydroxyl, carboxyl, and sulfonate groups, make it promising for use in composite conductive hydrogels. In this review, the source, structure, and reaction characteristics of industrial lignin are provided. Description of the preparation method (physical and chemical strategies) of lignin-based conductive hydrogel is elaborated along with their several important properties, such as electrical conductivity, mechanical properties, and porous structure. Furthermore, we provide insights into the latest research advances in industrial lignin conductive hydrogels, including biosensors, strain sensors, flexible energy storage devices, and other emerging applications. Finally, the prospects and challenges for the development of lignin-conductive hydrogels are presented. [ABSTRACT FROM AUTHOR]

Soda lignin is a by-product of the soda process for producing cellulose from grassy raw materials. Since a method for the industrial processing of lignin of this type is still lacking, several research teams have been working on solving this problem. We first propose a modification of soda lignin with sulfamic acid over solid catalysts. As solid catalysts for lignin sulfation, modified carbon catalysts (with acid sites) and titanium and aluminum oxides have been used. In the elemental analysis, it is shown that the maximum sulfur content (16.5 wt%) was obtained with the Sibunit-4® catalyst oxidized at 400 °C. The incorporation of a sulfate group has been proven by the elemental analysis and Fourier-transform infrared spectroscopy. The molecular weight distribution has been examined by gel permeation chromatography. It has been demonstrated that the solid catalysts used in the sulfation process causes hydrolysis reactions and reduces the molecular weight and polydispersity index. It has been established by the thermal analysis that sulfated lignin is thermally stabile at temperatures of up to 200 °C. According to the atomic force microscopy data, the surface of the investigated film consists of particles with an average size of 50 nm. The characteristics of the initial and sulfated β-O-4 lignin model compounds have been calculated and recorded using the density functional theory. [ABSTRACT FROM AUTHOR]

As one of the most abundant natural polymers in nature, polysaccharides have the potential to replace petroleum-based polymers that are difficult to degrade in paper coatings. Polysaccharide molecules have a large number of hydroxyl groups that can bind strongly with paper fibers through hydrogen bonds. Chemical modification can also effectively improve the mechanical, barrier, and hydrophobic properties of polysaccharide-based coating layers and thus can further improve the related properties of coated paper. Polysaccharides can also give paper additional functional properties by dispersing and adhering functional fillers, e.g., conductive particles, catalytic particles or antimicrobial chemicals, onto paper surface. Based on these, this paper reviews the application of natural polysaccharides, such as cellulose, hemicellulose, starch, chitosan, and sodium alginate, and their derivatives in paper coatings. This paper analyzes the improvements and influences of chemical structures and properties of polysaccharides on the mechanical, barrier, and hydrophobic properties of coated paper. This paper also summarizes the researches where polysaccharides are used as the adhesives to adhere inorganic or functional fillers onto paper surface to endow paper with great surface properties or special functions such as conductivity, catalytic, antibiotic, and fluorescence. [ABSTRACT FROM AUTHOR]