The Effect of DBD Plasma Activation Time on the Dyeability of Woven Polyester Fabric with Disperse Dye.

This study consists of two parts. In the first, the woven polyester fabric, after washing to remove lubricant oils, was treated with the dielectric barrier discharge (DBD) plasma at the short plasma exposure time (from 15 to 90 s). The effect of the plasma exposure time on the activation of the polyester fabric was assessed by the wicking height of the samples. The results show that the wicking height in the warp direction of the plasma-treated samples improved but was virtually unchanged in the weft direction. Meanwhile, although the tensile strength in the warp direction of the fabric was virtually unaffected despite the plasma treatment time up to 90 s, in the weft direction it increased slightly with the plasma treatment time. Scanning Electron Microscope (SEM) images and the X-ray Photoelectron Spectroscopy (XPS) spectra of the samples before and after the plasma treatment were used to explain the nature of these phenomena. Based on the results of the first part, in the second part, two levels of the plasma treatment time (30 and 60 s) were selected to study their effect on the polyester fabric dyeability with disperse dyes. The color strength (K/S) values of the dyed samples were used to evaluate the dyeability of the fabric. The SEM images of the dyed samples also showed the difference in the dyeability between the plasma-treated and untreated samples. A new feature of this study is the DBD plasma treatment condition for polyester fabrics. The first is the use of DBD plasma in air (no addition of gas). Second is the very short plasma treatment time (only 15 to 90 s); this condition will be very favorable for the deployment on an industrial scale.

Investigation of Mechanical, Chemical, and Antibacterial Properties of Electrospun Cellulose-Based Scaffolds Containing Orange Essential Oil and Silver Nanoparticles.

This study demonstrated a controllable release properties and synergistic antibacterial actions between orange essential oil (OEO) and silver nanoparticles (AgNPs) incorporated onto cellulose (CL) nanofibers. The preparation of AgNPs attached on CL nanofibers was conducted through multiple processes including the deacetylation process to transform cellulose acetate (CA) nanofibers to CL nanofibers, the in situ synthesis of AgNPs, and the coating of as-prepared silver composite CL nanofibers using OEO solutions with two different concentrations. The success of immobilization of AgNPs onto the surface of CL nanofibers and the incorporation of OEO into the polymer matrix was confirmed by SEM-EDS, TEM, XRD, and FT-IR characterizations. The tensile strength, elongation at break, and Young's modulus of the nanofibers after each step of treatment were recorded and compared to pristine CA nanofibers. The high antibacterial activities of AgNPs and OEO were assessed against Gram-positive B. subtilis and Gram-negative E. coli microorganisms. The combined effects of two antimicrobials, AgNPs and OEO, were distinctively recognized against E. coli.

Ion-interactions as driving force in polysaccharide assembly.

The structure of cellulose is characterised by extensive non-covalent interactions. Recent discussions suggest that hydrophobic interactions between polymer chains also play a significant role in governing cellulose solubility. Surprisingly in almost all cellulose shaping processes, chemical systems or solvents are applied, which base on melts or solutions of charged molecules. Ionic interactions play a significant role in the shaping and modification of cellulose based materials. Dependent on the systems used different principles govern the processes and define the results, e.g. formation of associates with alkali hydroxides, ion-exchange reactions to selectively bind multivalent ions at carboxylic groups, adsorption of dissolved polymers through surface charge neutralisation or metal complex formation, where cellulose takes the role of a polymer ligand system. Presence of charged compounds takes a significant role in cellulose swelling and dissolution, but also directs reassembly of polysaccharide material to solid three-dimensional structures.

Investigation of the spinnability of cellulose/alkaline ferric tartrate solutions.

Dynamic rheology, UV/VIS spectrometry with temperature programming cuvette and reaction calorimetry were conducted on cellulose pulp/FeTNa (NaOH solution containing ferric tartaric acid complex) solutions to investigate their thermostability and spinnability. Color of cellulose/FeTNa solutions changed above 90°C due to the decomposition of the complex. Thermal activity of cellulose/FeTNa solution started above 130°C induced by water vapor evolution and complex decomposition. Regeneration of cellulose/FeTNa solutions in a non-solvent (acetic acid and Na-gluconate mixture) resulted in transition from cellulose I into cellulose II structure as revealed by WAXS measurements. Wet-spinning attempts of cellulose/FeTNa solutions yielded fiber-like shaped bodies with a brittle structure.