High performance chitosan/nanocellulose-based composite membrane for alkaline direct ethanol fuel cells.

Polysaccharide anion exchange membranes (AEMs) containing chitosan (CS), cellulose nanofibrils (CNFs) and CNFs quaternized with poly(diallyldimethylammonium chloride) (CNF(P)s) were developed for use in alkaline direct ethanol fuel cells (ADEFCs). The resulting composite membranes prepared by the solvent casting process based on an experimental design were comprehensively assessed for morphology, KOH uptake, swelling ratio, EtOH permeability, mechanical properties, ionic conductivity, and cell performance. The fabricated CS-based composite membranes with CNF(P) fillers were superior to the commercial Fumatech FAA-3-50 membrane in terms of Young's modulus and tensile strength (69 % and 85 % higher, respectively), ion exchange capacity (169 % higher), and ionic conductivity (228 % higher). Single fuel cell tests have shown excellent performance of the CS-based membranes with CNF and CNF(P) fillers, as they exhibited up to 86 % improvement in power density at 80 °C compared to the commercial membrane (65.1 mW/cm2 vs. 35.1 mW/cm2) and higher maximum power density at all test conditions.

Cotton Woven Fabrics as Protective Polymer Materials against Solar Radiation in the Range of 210-1200 nm.

The proposed paper describes the influence of woven fabric constructional parameters (type of weave, relative fabric density) and colouration (obtained by eco-friendly dyeing) on the solar transmittance of cotton woven fabrics in the range of 210-1200 nm. The cotton woven fabrics in their raw state were prepared according to Kienbaum's setting theory, at three levels of relative fabric density and three levels of the weave factor, and then exposed to the dyeing process with natural dyestuffs (beetroot, walnut leaves). After ultraviolet/visible/near-infrared (UV/VIS/IRA) solar transmittance and reflection in the range of 210-1200 nm were recorded, the influence of the fabric construction and colouration were analysed. The guidelines for fabric constructor were proposed. The results show that the walnut-coloured satin samples at the third level of relative fabric density provide the best solar protection in the whole solar spectrum. All the tested eco-friendly dyed fabrics offer good solar protection, while only raw satin fabric at the third level of relative fabric density can be classified as solar protective material with even better protection in IRA region than some coloured samples.

Adsorption of Pollutants from Colored Wastewaters after Natural Wool Dyeing.

The presented study assesses the efficiency of selected adsorbents, zeolite 4A in two particle sizes and pelletized activated carbon (AC), for the potential removal of color, chemical oxygen demand (COD), total organic carbon (TOC) and metals from wastewaters after natural wool dyeing. Firstly, the natural coloring compounds were extracted from dried common walnut (Juglans regia) leaves and used further for exhaustion dyeing of wool fibers, together with three different metallic salts in two concentrations (meta-mordanting). Effluents with higher mordant concentration were additionally treated according to a shake-flask adsorption experiment. The obtained results revealed efficient removal of exceeded metallic ions by zeolite (up to 94.7%), on account of their superior ion exchange capability as compared to AC. The zeolites also reduced turbidity and electrical conductivity significantly. On the other hand, AC was more efficient for the reduction in organic pollution, COD up to 96% and TOC up to 95%, due to its higher specific surface area and total pore volume, and, thus, higher potential for adsorption of different compounds in comparison to 4A. All three proposed adsorbents lowered wastewaters' coloration remarkably, up to 78% (AC) and up to 71% (4A), depending on the type of effluent/mordant and inspected wavelength; although, the spectral absorbance coefficient (SAC) values remained highly above the limit values for discharge of wastewaters into watercourses.

Metallisation of Textiles and Protection of Conductive Layers: An Overview of Application Techniques.

The rapid growth in wearable technology has recently stimulated the development of conductive textiles for broad application purposes, i.e., wearable electronics, heat generators, sensors, electromagnetic interference (EMI) shielding, optoelectronic and photonics. Textile material, which was always considered just as the interface between the wearer and the environment, now plays a more active role in different sectors, such as sport, healthcare, security, entertainment, military, and technical sectors, etc. This expansion in applied development of e-textiles is governed by a vast amount of research work conducted by increasingly interdisciplinary teams and presented systematic review highlights and assesses, in a comprehensive manner, recent research in the field of conductive textiles and their potential application for wearable electronics (so called e-textiles), as well as development of advanced application techniques to obtain conductivity, with emphasis on metal-containing coatings. Furthermore, an overview of protective compounds was provided, which are suitable for the protection of metallized textile surfaces against corrosion, mechanical forces, abrasion, and other external factors, influencing negatively on the adhesion and durability of the conductive layers during textiles' lifetime (wear and care). The challenges, drawbacks and further opportunities in these fields are also discussed critically.

Efficiency of Differently Processed Membranes Based on Cellulose as Cationic Dye Adsorbents.

In order to minimize the pollution caused by the reuse of textile dyes, technologies and materials have been developed that purify waste water in an efficient and cost-effective manner before it is discharged into a water body. In this context, the presented research investigates the potential of two types of fully cellulose-based membranes as adsorbents for cationic dyes used in the textile industry. The first type combines cellulose nanofibrils (CNFs) and carboxymethylated cellulose (CMC) using the solvent casting process and an esterification coupling reaction, while the second type uses commercial bacterial cellulose (BC) in a native and sodium periodate-treated form (BCox). The corresponding membranes were comprehensively evaluated by means of Fourier Transform Infrared (FTIR) Spectroscopy. Results confirm the esterification process within the CNF/CMC membranes, as well as BC oxidation after periodate treatment, as shown by bands at 1726.2 cm-1 and 895 cm-1, respectively. The Potentiometric Titration shows the highest total negative charge of 1.07 mmol/g for 4CNF/4CMC, which is assigned to the presence of COO- within CMC polymers, and lowest (0.21 mmol/g) for BCox. The Contact Angle Goniometry data confirm the hydrophilicity of all membranes, and the angle increased from 0 ° (in pure BC) to 34.5 ° in CMC-rich and to 31.4 ° in BCox membranes due to the presence of CH2COO- and CHO groups, respectively. Confocal Fluorescent Microscopy (CFM) demonstrated the highest µ-roughness in 4CNF/4CMC, while Scanning Electron Microscopy (SEM) depicted diverse morphological features between the membranes, from ultrafine nanofiber networks (in BC and BCox) to larger fiber bundles connected within the polymer phase in CNF/CMC membranes. The adsorption experiment followed by UV-VIS spectroscopy, showed ~100% dye removal efficiency in both CNF/CMC-based membranes, while BC and BCox adsorbed only 24.3% and 23.6%, respectively, when anthraquinone dye was used. Azo dye was only adsorbed with an efficiency of 7-9% on CMC/CNF-based membranes, compared with 5.57% on BC and 7.33% on BCox membranes. The adsorption efficiency at equilibrium was highest for BC (1228 mg/g) and lowest for 7CNF/1CMC (419.24 mg/g) during anthraquinone dye adsorption. In the case of azo dye, the BCox was most effective, with 445.7 mg/g. Applicability of a pseudo second-order model was confirmed for both dyes and all membranes, except for BCox in combination with azo dye, showing the fastest adsorption rate in the case of the 7CNF/1CMC membrane.

Electrospun nanofibrous composites from cellulose acetate / ultra-high silica zeolites and their potential for VOC adsorption from air.

The optimized preparation of novel electrospun nanofibrous composites from cellulose acetate (CA) and ultra-high silica zeolites (UHSZ) are reported as a promising material for the adsorption of Volatile Organic Compound (VOCs). Two types of UHSZs, i.e. silicalite and USY were prepared by hydrothermal crystallization while the fabrication of composites was performed using single needle and needle-less electrospinning systems, demonstrating the scalability of the composite fibres' manufactured. Herein, factors such as properties of spinning solutions and electrospinning process parameters were studied, as well as interactions between the CA and UHSZs. In addition, Quartz Crystal Microbalance - Dissipation technique (QCM-D) was employed with an aim to study the adsorption behaviour of newly developed composites using ammonia as a model pollutant. The QCM-D data revealed that the presence of UHSZs in the CA materials increased adsorption capacity, designating CA/UHSZ composites as potential materials suitable for a large-scale removal of VOCs from polluted air.

Thermal, Mechanical and Optical Features of Aluminosilicate-Coated Cotton Textiles via the Crosslinking Method.

The presented study focuses on the development of a pad-dry-thermofix functional coating process using a mixture of microporous aluminosilicate particles in diverse bath formulations to impart UV-ray-blocking, thermal stability and easy-care properties to the cotton fabric. The results of Scanning Electron Microscopy (SEM) and X-ray powder Diffraction (XRD) revealed the presence of three different types of zeolites within the examined sample, i.e., the largest amount being zeolite A, followed by the zeolite X, and the zeolite ZSM-5. The surface characterization results of zeolite-coated/cross-linked textiles provided evidence of acceptable UV-ray-blocking properties and increased thermal stability, as well as enhanced tensile strength and breaking tenacity without considerably decreasing the whiteness degree. Moreover, the dry crease recovery angle increased for the cotton fabric cross-linked via an mDMDHEU, and decreased significantly using 30 g/L zeolites negatively influencing qualitative values. TG/DTA results have proven the enlarged thermal stability of aluminosilicate-coated cotton, although combustion was not prevented.

Enhanced catalytic activity of the surface modified TiO2-MWCNT nanocomposites under visible light.

Fusing multiwall carbon nanotubes (MWCNTs) with TiO2 at the nano-scale level promotes the separation of those electron-hole charges generated upon UV and daylight irradiation. In this study, we investigated facile sonochemical synthesis, combined with the calcination process for the preparations of TiO2-MWCNT composites with different mole ratios of titanium and carbon. In order to produce stable nano dispersions we exploited an innovative biotechnology-based approach for the covalent functionalizations of TiO2-MWCNTs with in-situ synthesized soluble phenoxazine dye molecules. The none and functionalized TiO2-MWCNTs composites were analyzed by a range of analytical techniques including XRD, Raman, XPS, SEM and UV-vis diffuse reflectance spectroscopy (DRS), and dynamic light scattering (DLS). The photocatalytic activity was evaluated toward the liquid-phase degradation of MB in aqueous solution under both UV and visible light irradiation. TiO2-MWCNTs with optimized mole ratio exhibit much higher photocatalytic activity and stability than bare TiO2. The as-prepared TiO2-MWCNTs photocatalyst possessed good adsorptivity of dyes, extended light absorption range and efficient charge separation properties simultaneously. The results indicated that the soluble phenoxazine dyes and amino-benzenesulfonic acid monomers were covalently grafted on to the surfaces of TiO2-MCNTs, which promoted good aquatic dispersibility and extended light absorption, resulting in increased photocatalytic efficiency.

Analysis of reactive dyestuffs and their hydrolysis by capillary electrophoresis.

The objective of the presented research was to examine the potential of capillary electrophoresis (CE) for the analysis of structurally different reactive dyestuffs, their activation and posterior hydrolysis, with special focus on optimization of the working conditions. Preliminary, the effect of various additives to the background electrolyte on the resolution improvements versus migration time of Reactive Black 5 as a model dyestuff was investigated. Based on these results, the electropherograms of eight commercially interesting reactive dyestuffs of various chemical structures and their converted forms upon alkaline pH were carried-out. In order to examine the behavior of the reactive dyestuff during the dyeing process, the dye-bath absorbance was monitored throughout the Reactive Black 5 exhaustion, and the conversion of the dye's form was highlighted using the CE technique. The obtained results unequivocally prove that CE could offer a fast and efficient detection method of structurally different reactive dyestuffs, as well as their hydrolysis products in the dye-baths and effluents later on.