Synthesis and Superficial Modification "In Situ" of Copper Selenide (Cu2-x Se) Nanoparticles and Their Antibacterial Activity.

Copper selenide nanoparticles (Cu2-x Se NPs) have received a lot of attention in recent decades due to their interesting properties and potential applications in various areas such as electronics, health, solar cells, etc. In this study, details of the synthesis and characterization of copper selenide nanoparticles modified with gum arabic (GA) are reported. Also, through transmission electronic microscopy (TEM) analysis, the transformation of the morphology and particle size of copper selenide nanoparticles in aqueous solution was studied. In addition, we present an antimicrobial study with different microorganisms such as Staphylococcus aureus (S. aureus), Escherichia coli (E. coli) and Candida albiacans (C. albicans). Copper selenide nanoparticles were characterized by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), differential scanning calorimetry analysis (DSC) and TEM. XRD confirmed the crystal-line structure of the nanoparticles such as cubic berzelanite with a particle size of 6 nm ± 0.5. FTIR and TGA corroborated the surface modification of copper selenide nanoparticles with gum arabic, and DSC suggested a change in the structural phase from cubic to hexagonal. TEM analysis demonstrated that the surface modification of the Cu2-x Se NPs stabilized the nanostructure of the particles, preventing changes in the morphology and particle size. The antimicrobial susceptibility analysis of copper selenide nanoparticles indicated that they have the ability to inhibit the microbial growth of Staphylococcus aureus, Escherichia coli and Candida albicans.

Functional Technical Textile-Based Polymer Nanocomposites with Adsorbent Properties of Toxins and Dyes also Have Antibacterial Behavior.

This is the first study of non-woven fabrics elaborated by melt-blowing from polymer nanocomposites made of Nylon 6 and nanoclay (Cloisite 20A) modified with an amine (1,4 diaminobutane dihydrochloride). Morphological and physical characteristics, adsorption capacity, and antibacterial properties are presented. From the X-ray diffraction (XRD) results, it was possible to observe a displacement of the signals to other 2θ angles, due to an α to ϒ phase shift. The scanning electron microscopy (SEM) images showed that the mean diameter of fiber decreased as the content of nanoclay increased. The mechanical tests showed that the tear strength force of neat nylon was 1.734 N, but this characteristic increased to 2.135 N for the sample with 0.5% modified nanoclay. The inulin adsorption efficiency of the Nylon 6/C20A 1.5% and Nylon 6/C20A 2% samples at 15 min was 75 and 74%, respectively. The adsorption capacity of Nylon 6/C20A 1.5% and Nylon 6/C20A 2% for methylene blue and methyl orange remained above 90% even after four adsorption cycles. In addition, non-woven fabrics present antibacterial activity against E. coli.

Green Flame-Retardant Blend Used to Improve the Antiflame Properties of Polypropylene.

The flammability properties of polymers and polymeric composites play an important role in ensuring the safety of humans and the environment; moreover, flame-retardant materials ensure a greater number of applications. In the present study, we report the obtaining of polypropylene (PP) composites contain a mixture of two green flame retardants, lignin and clinoptilolite, by melt extrusion. These additives are abundantly found in nature. Fourier transform infrared (FT-IR), thermogravimetric analysis (TGA), mechanical properties, scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDS), cone calorimetry, UL-94, and carbonized residues analysis were carried out. TGA analysis shows that PPGFR-10 and PPGFR-20 compounds presented better thermal stability with respect to PP without flame retardants. The conical calorimetric evaluation of the composites showed that PPGFR-10 and PPGFR-20 presented decreases in peak heat release rates (HRRs) of 9.75% and 11.88%, respectively. The flammability of the composites was evaluated with the UL-94 standard, and only the PPGFR-20 composite presented the V-0 and 5VB classification, which indicates good flame-retardant properties. Additives in the polymer matrix showed good dispersion with few agglomerates. The PPGFR-20 composite showed an FRI value of 1.15, higher percentage of carbonized residues, and UL-94 V-0 and 5VB rating, suggesting some kind of synergy between lignin and clinoptilolite, but only at high flame-retardant concentrations.

Influence of Modified Carbon Black on Nylon 6 Nonwoven Fabric and Performance as Adsorbent Material.

The number of chronic kidney disease (CKD) persons continues to rise in Mexico. They require renal replacement therapy, and in the absence of it, hemodialysis is the major option for their survival. The uremic toxins present in the blood are removed by hemodialysis, which involve membranes. In this study, nonwoven fabrics with modified carbon black nanoparticles in a matrix polymer of Nylon 6 were obtained and evaluated as an adsorbent material of uremic toxins. All nonwoven fabrics were characterized by FTIR, XRD, TGA, SEM, and contact angle measurements and were evaluated as an adsorbent material for the urea toxin and as an albumin retainer. The findings suggest their potential application as a hemodialysis membrane. Nanocomposites had a higher hydrophilic characteristic compared to pure Nylon 6. The average diameter size of the fibers was in the range of 5 to 50 µm. All nanocomposites nonwoven fabrics showed high removal percentages of inulin in a range of 80-85% at 15 min of contact. Most Ny6 Zytel/CB nanocomposites showed a high percentage of urea removal (80 to 90%).

PLA-ZnO/TiO2 Nanocomposite Obtained by Ultrasound-Assisted Melt-Extrusion for Adsorption of Methylene Blue.

Access to fresh water is an increasing concern worldwide. The contamination of this vital liquid is largely caused by discharges of pollutants into rivers and seas from different types of industries. Waste dyes from different industries have been classified as harmful to health. In this study, polymeric nanomaterials based on polylactic acid (PLA) and nanoparticles of titanium dioxide (TiO2) and zinc oxide (ZnO) modified by ultrasound-assisted extrusion were obtained. These materials were evaluated by FTIR, DRX, TGA, DSC, SEM and methylene blue adsorption. From the results of the physicochemical characterizations, it was possible to observe the presence of TiO2 and ZnO nanoparticles dispersed in the polymeric matrix, increasing the crystallinity and thermal stability of the polymer. In addition, a good dispersion of the nanoparticles could be seen by means of SEM, due to the extrusion assisted by ultrasound. The methylene blue dye adsorption tests revealed that the best result was 98% dye adsorption in a time of 13 min for the 1.5% PZT sample. Additionally, this material could be used for 3 adsorption cycles without affecting its adsorbent properties.

Green Flame-Retardant Composites Based on PP/TiO2/Lignin Obtained by Melt-Mixing Extrusion.

Nowadays, highly flammable and harmful plastic materials are used in many daily applications. To prevent burning of materials, other harmful molecules or materials that are not environmentally friendly are added to plastics. To overcome this environmental issue, new materials have been investigated. Lignin, an industrial by-product, is an abundant biopolymer that can be used in fire safety plastics; it is considered a renewable and readily available resource. In this work, PP-TiO2/lignin composites were obtained with TiO2/lignin mixtures through the melt extrusion process, with different weight percentages of nanoparticles (10, 20, 25, and 30 wt.%). The PP-TiO2/lignin composites were characterized by XRD, FTIR, TGA, and SEM. Furthermore, cone calorimetry tests and the mechanical properties were evaluated. Cone calorimetry tests revealed that the introduction of 25 wt.% TiO2-lignin to the PP matrix reduced the peak of heat release rate (PHRR) and total heat release (THR) by 34.37% and 35.45%, respectively. The flame retardancy index (FRI) values of the composites were greater than 1.0 and were classified as good; the highest value of 1.93 was obtained in the PP-30 sample. The tensile tests demonstrated that the flexural modulus of the composites increased gradually with increasing lignin and TiO2 content, and the flexural strength decreased slightly. The use of lignin in PP composites can be an excellent alternative to synthesize new materials with improved flame-retardant properties and which is friendly to the environment.

Synthesis of Copper Nanoparticles Stabilized with Organic Ligands and Their Antimicrobial Properties.

In this work, we report the synthesis of copper nanoparticles (Cu NPs), employing the chemical reduction method in an aqueous medium. We used copper sulfate pentahydrate (CuSO4·5H2O) as a metallic precursor; polyethylenimine (PEI), allylamine (AAM), and 4-aminobutyric acid (AABT) as stabilizing agents; and hydrated hydrazine as a reducing agent. The characterization of the obtained nanoparticles consisted of X-ray, TEM, FTIR, and TGA analyses. Through these techniques, it was possible to detect the presence of the used stabilizing agents on the surface of the NPs. Finally, a zeta potential analysis was performed to differentiate the stability of the nanoparticles with a different type of stabilizing agent, from which it was determined that the most stable nanoparticles were the Cu NPs synthesized in the presence of the PEI/AAM mixture. The antimicrobial activity of Cu/PEI/AABT toward P. aeruginosa and S. aureus bacteria was high, inhibiting both bacteria with low contact times and copper concentrations of 50-200 ppm. The synthesis method allowed us to obtain Cu NPs free of oxides, stable to oxidation, and with high yields. The newly functionalized Cu NPs are potential candidates for antimicrobial applications.

Green Synthesis of Copper Nanoparticles Using Cotton.

Copper nanoparticles (CuNP) were obtained by a green synthesis method using cotton textile fibers and water as solvent, avoiding the use of toxic reducing agents. The new synthesis method is environmentally friendly, inexpensive, and can be implemented on a larger scale. This method showed the cellulose capacity as a reducing and stabilizing agent for synthetizing Cellulose-Copper nanoparticles (CCuNP). Nanocomposites based on CCuNP were characterized by XRD, TGA, FTIR and DSC. Functional groups present in the CCuNP were identified by FTIR analysis, and XRD patterns disclosed that nanoparticles correspond to pure metallic Cu°, and their sizes are at a range of 13-35 nm. Results demonstrated that CuNPs produced by the new method were homogeneously distributed on the entire surface of the textile fiber, obtaining CCuNP nanocomposites with different copper wt%. Thus, CuNPs obtained by this method are very stable to oxidation and can be stored for months. Characterization studies disclose that the cellulose crystallinity index (CI) is modified in relation to the reaction conditions, and its chemical structure is destroyed when nanocomposites with high copper contents are synthesized. The formation of CuO nanoparticles was confirmed as a by-product, through UV spectroscopy, in the absorbance range of 300-350 nm.

Synthesis of Nylon 6/Modified Carbon Black Nanocomposites for Application in Uric Acid Adsorption.

High uric acid levels cause different clinic conditions. One of them is hyperuricemia, which leads to kidney damage. A solution for eliminating uric acid in the blood is by hemodialysis, which is performed using nanocomposite membranes. In this work, Nylon 6 nanocomposites were synthesized with modified carbon black (MCB), which were considered candidate materials for hemodialysis membranes. The modification of carbon black was made with citric acid using the variable-frequency ultrasound method. The new MCB was characterized by Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), X-ray diffraction (XRD), transmission electron microscopy (TEM), and dispersion tests. Nylon 6/MCB nanocomposites were processed using the ultrasound-assisted melt-extrusion method to improve the dispersion procedure of the nanoparticles. The Nylon 6/MCB nanocomposites were characterized by FTIR, TGA, and differential scanning calorimetry (DSC). These were assessed for the absorption of toxins and hemocompatibility. MBC and nanocomposites showed excellent uric acid removal (78-82%) and hemocompatibility (1.6-1.8%). These results suggest that Nylon 6/MCB nanocomposites with low loading percentages can be used on a large scale without compatibility problems with blood.

Pigmentation and Degradative Activity of TiO2 on Polyethylene Films Using Masterbatches Fabricated Using Variable-Frequency Ultrasound-Assisted Melt-Extrusion.

Ultrasound-assisted melt-extrusion method (USME) is a high-quality process used to produce polymeric compounds with an adequate homogeneous dispersion. This study evaluates white-color films of linear low-density polyethylene (LLDPE) prepared using TiO2 masterbatch obtained by ultrasound-assisted melt-extrusion at variable frequencies (USME-VF). LLDPE with three different melt-flow indices (2, 20 and 50 g/10 min) were used as the polymer matrix. The films were obtained from the dilution of masterbatches of LLDPE (melt-flow index = 2) at a concentration of 7 wt% TiO2. The morphology, pigmentation, TiO2 reactivity, and the mechanical stability of the films were assessed. The masterbatch compounds were evaluated by melt-flow index (MFI) and scanning electron microscopy (SEM). The contrast ratio, yellowness index and mechanical properties of films were also measured. The properties of whiteness and elongation at break improved in the films prepared using masterbatches with higher dispersion. Though the reactivity of the TiO2 particles increased during accelerated aging, it did not affect the elongation to rupture. The yellowness index was moderately affected in films that included TiO2 particles processed using USME-VF.

Dióxido de zirconio: alternativas de síntesis y aplicaciones biomédicas / Zirconium dioxide: synthesis alternatives and biomedical applications

Resumen Entre los diferentes materiales cerámicos, el dióxido de zirconio (ZrO2) se destaca, debido a sus aplicaciones en el área médica, química y farmacéutica. Esto es posible al ser un material de carácter anfótero, con tres fases cristalinas: monoclínica, tetragonal y cúbica, las cuales presentan distintas propiedades. El objetivo de este trabajo fue analizar los fundamentos de los diferentes métodos utilizados para la síntesis del ZrO2 y sus aplicaciones biomédicas. Las principales metodologías empleadas son los procesos hidrotérmico, precipitación, solvotérmica y sol-gel. La energía de ultrasonido y la radiación de microondas permiten reducir los tiempos de reacción y proporcionar mayor eficiencia energética a los procesos. El método de síntesis modifica las propiedades del ZrO2, lo cual es aprovechado para desarrollar diferentes aplicaciones, entre ellas destacan reemplazos óseos, prótesis dentales y liberación de fármacos.

Abstract Among the different ceramic materials, zirconium dioxide (ZrO2) stands out, due to its applications in the medical, chemical and pharmaceutical areas. This is possible, since it is an amphoteric material with three crystalline phases: monoclinic, tetragonal and cubic, which have different properties. The objective of this work was to analyze the fundamentals of the different methods used for the synthesis of ZrO2, and its main biomedical applications. The main methodologies used include the hydrothermal, precipitation, solvothermal and sol-gel processes. The use of ultrasound energy and microwave radiation allows the reduction in reaction times, and provides greater energy efficiency to the process and a lower environmental impact. The synthesis method modifies the properties of ZrO2, which is used to develop different applications, including bone replacements, dental prostheses and drug release.