Films of chitosan and natural modified hydroxyapatite as effective UV-protecting, biocompatible and antibacterial wound dressings

Chitosan is a natural polysaccharide widely used in biomedicine, for instance for wound dressing. Hydroxyapatite is a very bioactive calcium phosphate which, if modified with an appropriate element (iron Fe), can also have UV-absorbing properties. In this work, we report the study of films of chitosan incorporated with iron-modified hydroxyapatite of natural origin (from cod fish bones); this combination led to an innovative chitosan-based material with excellent and advanced functional properties. The films showed very high UV absorption (Ultraviolet Protection Factor (UPF) value higher than 50). This is the first time that a chitosan-based material has shown such high UV protection properties. The films also showed to be non-cytotoxic, and possessed antimicrobial activity towards both Gram-positive and negative strains. Their mechanical properties, optimised with an experimental design approach, confirmed their potential use as multifunctional wound dressing, capable of reducing bacterial infections and, at the same time, protecting from UV light

Effective removal of anionic and cationic dyes by kaolinite and TiO2/kaolinite composites

The present study investigated the removal of methylene blue (MB) and orange II (OII) dyes from synthetic wastewater by means of adsorption and photocatalysis using natural kaolins. For MB adsorption, the raw kaolinite-rich samples showed the greatest adsorption capacity, with rapid uptake (90% after 20 min). The experimental results were fitted better using the Langmuir isotherm model parameters compared to the Freundlich model, suggesting that the adsorption corresponds to monolayer coverage of MB molecules over the kaolinite surface. For OII, neither the Langmuir nor the Freundlich model gave reliable results, because the adsorption of anionic dye molecules by the clayey particles is not favoured. Mixtures of kaolinite/Degussa TiO2 were also prepared, and their photocatalytic properties under UV-light exposure were investigated. Decolourization of MB solutions was observed, even in a mixture with low TiO2 content. This is related to the combined effect of adsorption and photocatalysis and, unlike the pure clay samples, the efficiency of such mixtures against OII was only slightly weaker (80-94%). For TiO2-impregnated clays, with the kaolinite layers separated by sol-gel TiO2 particles, the MB removal was slow and effective only after >24 h due to the complexity of the bonding of MB molecules. On the other hand, the removal performance against OII solutions was very efficient (nearly 100%) within only 2 h. This excellent performance was attributed to morphological changes in clay particles

Chitosan-hydroxyapatite composites made from sustainable sources: a morphology and antibacterial study

Chitosan (Cs) and hydroxyapatite (HA) 3D scaffolds/composites were prepared with a sustainable process, as HA was obtained using CaCO3 derived from cork, a natural material used as a template agent. The HA@Cs composites were prepared with HA in situ formation in a Cs solution, with a dissolution-precipitation mechanism. Different reaction times were considered, with time of 72 h leading to the best materials (sample CsHA_72). X-ray Diffraction (XRD) analysis confirmed HA formation. The analysis of Cs unit cell parameters showed that, for the unmodified Cs, the cell had larger dimensions and a higher degree of distortion than previously reported in literature; HA incorporation in the CsHA_72 composite led to a further increase in the cell dimensions. The morphology of the scaffolds was studied with Scanning Electron Microscopy (SEM) and a high level of porosity was observed; a statistical comparison was performed between the unmodified Cs and CsHA_72 to determine the pore size, structure, and distribution. This analysis, the first of this kind for this type of composites, showed smaller and more circular pores for the CsHA_72 composite (average diameter of 70 μm vs. 88 μm for unmodified Cs). The overall level of porosity, however, did not change (>77%); likewise, the Young modulus was not affected by HA incorporation (about 11 kPa). Antibacterial tests, performed on Escherichia coli and Staphylococcus aureus, showed that HA presence did not significantly reduce the antimicrobial properties; the composites were particularly effective towards S. aureus, as a >90% the bacterial population reduction was observed for an incubation time of 2 h. HA@Cs also showed excellent biocompatibility and good cell proliferation. The properties of these 3D scaffolds make them suitable for application as biomaterials.info:eu-repo/semantics/publishedVersio

Photocatalytic removal of benzene over Ti3C2Tx MXene and TiO2–MXene composite materials under solar and NIR irradiation

MXenes, a family of two-dimensional (2D) transition metal carbides, nitrides and carbonitrides based on earth-abundant constituents, are prospective candidates for energy conversion applications, including photocatalysis. While the activity of individual MXenes towards various photocatalytic processes is still debatable, these materials were proved to be excellent co-catalysts, accelerating the charge separation and suppressing the exciton recombination. Titanium-containing MXenes are well compatible with the classical TiO2 photocatalyst. The TiO2 component can be directly grown on MXene sheets by in situ oxidation, representing a mainstream processing approach for such composites. In this study, an essentially different approach has been implemented: a series of TiO2-MXene composite materials with controlled composition and both reference end members were prepared, involving two different strategies for mixing sol-gel-derived TiO2 nanopowder with the Ti3C2Tx component, which was obtained by HF etching of self-propagating high-temperature synthesis products containing modified MAX phase Ti3C2Alz (z > 1) with nominal aluminium excess. The prospects of such composites for the degradation of organic pollutants under simulated solar light, using benzene as a model system, were demonstrated and analysed in combination with their structural, microstructural and optical properties. A notable photocatalytic activity of bare MXene under near infrared light was discovered, suggesting further prospects for light-to-energy harvesting spanning from UV-A to NIR and applications in biomedical imaging and sensors.publishe

Synthesis and characterization of Sn‑doped TiO2 flm for antibacterial applications

Simple sol–gel method has been exploited to deposit Sn-doped TiO2 thin flms on glass substrates. The resultant coatings were characterized by X-ray difraction (XRD), UV–visible techniques (UV–Vis), Fourier transform infrared spectroscopy (FTIR), and photoluminescence analysis (PL). The XRD pattern reveals an increase in crystallite size of the prepared samples with the increasing doping concentration. A decrease in doping concentrating resulted in the decrease in bandgap values. The diferent chemical bonds on these flms were identifed from their FTIR spectra. The photoluminescence analysis shows an increase in the emission peak intensity with increasing dopant concentration, and this can be attributed to the efect created due to surface states. The prepared samples were tested as antibacterial agent toward both Gram-positive and Gram-negative bacteria like S.aureus (Staphylococcus aureus) and E.coli (Escherichia coli), respectively. The size of the inhibition zones indicates that the sample shows maximum inhibitory property toward E.coli when compared to S.aureus

Dielectrical Properties of CeO2 Nanoparticles at Different Temperatures

A template-free precipitation method was used as a simple and low cost method for preparation of CeO2 nanoparticles. The structure and morphology of the prepared nanoparticle samples were studied in detail using X-ray diffraction, Raman spectroscopy and Scanning Electron Microscopy (SEM) measurements. The whole powder pattern modelling (WPPM) method was applied on XRD data to accurately measure the crystalline domain size and their size distribution. The average crystalline domain diameter was found to be 5.2 nm, with a very narrow size distribution. UV-visible absorbance spectrum was used to calculate the optical energy band gap of the prepared CeO2 nanoparticles. The FT-IR spectrum of prepared CeO2 nanoparticles showed absorption bands at 400 cm(-1) to 450 cm(-1) regime, which correspond to CeO2 stretching vibration. The dielectric constant (er) and dielectric loss (tan delta) values of sintered CeO2 compact consolidated from prepared nanoparticles were measured at different temperatures in the range from 298 K (room temperature) to 623 K, and at different frequencies from 1 kHz to 1 MHz

Mix design and mechanical performance of geopolymeric binders and mortars using biomass fly ash and alkaline effluent from paper-pulp industry

This work investigates the use of biomass fly ash (BFA) and an alkaline effluent (AEF), both generated from the Kraft pulp industry, in the preparation of geopolymeric binders and mortars for construction applications. BFA replaced the metakaolin (MK) while the AEF substituted the distilled water used to dissolve NaOH pellets. The mix design aims to maximize the amount of both the wastes and to optimize the materials properties, such as workability and mechanical performance. At the same time, also the environmental impact decreases enhancing the materials’ sustainability and facilitating the circular economy. For the previously optimized BFA/MK ratio (70/30 wt.%) several NaOH/Na2SiO3 ratios and water to AEF substitutions were tested. The best performance was achieved for the alkaline activator having one part of NaOH and three parts of Na2SiO3. According to the main results, the biologic AEF can totally replace the distilled water in the NaOH preparation. Thus will increase the sustainability of the novel materials. Subsequently, the optimized binder was used – with and without AEF - to manufacture mortars with various binder/aggregate ratios. It is concluded that the formulations with a binder/aggregate mass proportion of 1:3 showed the best mechanical performance (compressive strength surpassing 20 MPa, class M20) and the replacement of distilled water with AEF did not affect the specimens final properties, but enhance the materials sustainability. Furthermore, in the pursuit of sustainability, manufacture and curing were conducted at ambient conditions (20 °C, 65% RH), avoiding any external source of energy, involving simple, reproducible, and low-cost processes

Pseudobrookite ceramic pigments: Crystal structural, optical and technological properties.

Pseudobrookite pigments were synthesized by the conventional ceramic route, calcining at 1300 C four mixts., with a Fe2O3:TiO2 ratio ranging from 47:53 to 40:60, and were characterised by XRPD, DRS and coloring performance in several ceramic matrixes. Titania in moderate excess of the Fe2TiO5 stoichiometry, necessary to minimise the occurrence of unreacted precursors, induced lattice parameters smaller than ideal pseudobrookite, in agreement with the different radii of Ti4+ and Fe3+ ions. These pigments exhibit a peculiar, intensely brown coloration originated by several light absorptions in the visible spectrum due to both d5 electronic transitions and a magnetically-coupled paired transition between iron ions in adjacent lattice sites. A doubling of the 6A1  4T1 and 4T2 bands is related to the occurrence of Fe3+ in both octahedral sites of pseudobrookite. Besides, distinct metal-oxygen distances imply different energy absorptions in good accordance with the crystal field theory, despite the strongly covalent character of the Fe-O bonding. Although an entropy-stabilized phase, pseudobrookite persists dispersed in glazes and glassy coatings even after fast firing at 1200 C, so being suitable as ceramic pigment. However, its coloring performance depends on the chemico-phys. properties of ceramic matrixes: satd. brown shades achieved in low temp. glasses shift to a lighter brown in opacified glazes and fade to a light gray in wall tile glazes, where the high CaO and ZnO content contributes to rapidly dissolve pseudobrookite

Fully quantitative X-ray characterisation of Evonik Aeroxide TiO 2 P25®

Photocatalysis with TiO2 is one of the most promising methods for combatting environmental pollution. Of commercially available photocatalysts, Evonik Aeroxide (formerly Degussa) P25® titania is probably the most extensively used. In this communication, we quantitatively characterise the full phase composition (both crystalline and amorphous content) of P25®, as well as the microstructure of individual phases (crystalline domain size distribution and dislocation density). This was achieved with advanced X-ray diffraction (XRD) methods: Rietveld-RIR and whole powder pattern modelling (WPPM). Quantitative phase analysis (QPA) showed the precise composition of P25 to be 76.3 wt% anatase, 10.6 wt% rutile and 13.0 wt% amorphous, and microstructural details are given for the two crystalline phases. © 2014 Elsevier B.V