Search

In recent decades, interest in oxide nanomaterials with multifunctional properties has grown significantly. Titanium dioxide undoubtedly belongs to them, characterized by exceptional photocatalytic activity, non-toxicity, high availability, biocompatibility, antibacterial properties, and low cost. The treatment of textile materials with TiO2 nanoparticles is relatively simple, but the insufficient bonding efficiency between certain fibers and TiO2 nanoparticles creates a problem regarding the stability and durability of the nanocomposites. In this study, an attempt was made to improve the properties of cotton modified with gelatin hydrogel, which was cross-linked by glutaraldehyde, and incorporated titanium nanoparticles. Three modification methods were applied, varying the mixing regimes of the components and the conditions. The composite materials were investigated via SEM, FTIR, UV-Vis and elemental analysis. For the first time, titanium nanoparticles obtained by the reduction of TiO2 with oxalic acid were used to modify cotton. Cotton samples were modified with gelatin hydrogel cross-linked with glutaraldehyde to increase the active groups of cellulose fibers that bind to Ti ions. Using the hydrogel, the nanoparticles are deposited on the surface of the textile substrate. The elemental analysis shows the presence of TiO2 nanoparticles. Lines for Ti atoms appear, which is evidence that the particles retain their composition after immobilization. Microscopic analyzes showed that TiO2 nanoparticles were distributed unevenly in the cotton matrix. In the UV analysis, the appearance of a new absorption at 890 cm-1 was observed due to the attachment of Ti-NPs. The appearance of the IR peak at 878 cm-1 confirms the formation of chelate complexes of the nanoparticles in the composite material. [ABSTRACT FROM AUTHOR]

Climate change, waste disposal challenges, and emissions generated by the manufacture of non-renewable materials are driving forces behind the production of more sustainable composite materials. All-cellulose composites (ACCs) originate from renewable biomass, such as trees and other plants, and are considered fully biodegradable. Dissolving cellulose is a common part of manufacturing ACCs, and currently there is a lot of research focused on effective, but also more environmentally friendly cellulose solvents. There are several beneficial properties of ACC materials that make them competitive: light weight, recyclability, low toxicity, good optical, mechanical, and gas barrier properties, and abundance of renewable plant-based raw material. The most prominent ACC applications are currently found in the food packing, medical, technical and vehicle industries. All-cellulose nanocomposites (ACNCs) expand the current research field and can offer a variety of more specific and functional applications. This review provides an overview of the manufacture of sustainable ACCs from lignocellulose, purified cellulose, and cellulosic textiles. There is an introduction of the cellulose dissolution practices of creating ACCs that are currently researched, the structure of cellulose during complete or partial dissolution is discussed, and a brief overview of factors which influence composite properties is presented. [ABSTRACT FROM AUTHOR]

Abstract This work deals with provision and characterization of the biopolymer-based composites achieved by incorporation of cellulose fibers as the reinforcement within the glycerol plasticized matrix formed by thermoplastic cornstarch biopolymer. The function of starch-based polymers is limited due to poor mechanical properties. However, it is improved with forming a biocomposite of thermoplastic starch (TPS) as matrix and the cellulose fibers (CF) as reinforcement. The surface of cellulose fibers is successfully modified using the air plasma treatment with the aim of improving the matrix/fiber adhesion. The modified fibers are studied using X-ray diffraction (XRD), scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). The TPS/CF composites are prepared using high friction and hot compression procedure. Tensile test results and SEM images of the fracture surfaces show significant improvement of adhesion between treated cellulose fibers and TPS matrix. Thermogravimetric analysis shows a considerable decomposition at approximately 250–350 °C. XRD proved the significant increase in crystallinity percentage of composites compared to TPS. [ABSTRACT FROM AUTHOR]