Nanostructured Copper Selenide Coatings for Antifouling Applications.

The accumulation of microorganisms, plants, algae, or small animals on wet surfaces that have a mechanical function causes biofouling, which can result in structural or other functional deficiencies. The maritime shipping industry must constantly manage biofouling to optimize operational performance, which is a common and long-lasting problem. It can occur on any metal structure in contact with or submerged in ocean water, which represents additional costs in terms of repairs and maintenance. This study is focused on the production of antifouling coatings, made with nanoparticles of copper selenide (CuSe NPs) modified with gum arabic, within a water-base acrylic polymeric matrix. During the curing of the acrylic resin, the CuSe NPs remain embedded in the resin, but this does not prevent the release of ions. The coatings released copper and selenium ions for up to 80 days, and selenium was the element that was released the most. The adhesion of film coatings to metallic substrates showed good adhesion, scale 5B (ASTM D3359 standard). Antimicrobial activity tests show that the coatings have an inhibitory effect on Escherichia coli and Candida albicans. The effect is more noticeable when the coating is detached from the substrate and placed on a growing medium, compared to the coating on a substrate. Scanning electron microscopy (SEM) observations show that nanostructured CuSe coatings are made up of rod-shaped and spherical particles with an average particle size of 101.6 nm and 50 nm, respectively. The energy dispersive X-ray spectroscopy (EDS) studies showed that the ratio of selenium nanoparticles is greater than that of copper and that their distribution is homogeneous.

Production and Incorporation of Calcium-Hydrolyzed Nanoparticles in Alkali-Activated Mine Tailings.

This work presented the production and incorporation of calcium-hydrolyzed nano-solutions at three concentrations (1, 2, and 3 wt.%) in alkali-activated gold mine tailings (MTs) from Arequipa, Perú. As the primary activator solution, a sodium hydroxide (NaOH) solution at 10 M was used. Calcium-hydrolyzed nanoparticles with a particle size of 10 nm were localized inside self-assembled molecular spherical systems (micelles) with diameters of less than 80 nm that were well-dispersed in aqueous solutions and acted as secondary activator, and also as additional calcium resource for alkali-activated materials (AAMs) based on low-calcium gold MTs. High-resolution transmission electron microscopy/energy-dispersive X-ray spectroscopy (HR-TEM/EDS) analyses were carried out to characterize the morphology, size, and structure of the calcium-hydrolyzed nanoparticles. Fourier transform infrared (FTIR) analyses were then used to understand the chemical bonding interactions in the calcium-hydrolyzed nanoparticles and in the AAMs. Scanning electron microscopy/energy-dispersive X-ray spectroscopy (SEM/EDS) and quantitative X-ray diffraction (QXRD) were performed to study the structural, chemical, and phase compositions of the AAMs; uniaxial compressive tests evaluated the compressive strength of the reaction AAMs; and nitrogen adsorption-desorption analyses measured porosity changes in the AAMs at the nanostructure level. The results indicated that the main cementing product generated was amorphous binder gel with low quantities of nanostructured C-S-H and C-A-S-H phases. The surplus production of this amorphous binder gel produced denser AAMs at the micro-level and nano-level (macroporous systems). In addition, each increase in the concentration of calcium-hydrolyzed nano-solution had a direct/proportional effect on the mechanical properties of the AAM samples. AAM with 3 wt.% calcium-hydrolyzed nano-solution had the highest compressive strength, with a value of 15.16 MPa, which represented an increase of 62% compared with the original system without nanoparticles that were aged under the same conditions at 70 °C for seven days. These results provided useful information about the positive effect of calcium-hydrolyzed nanoparticles on gold MTs and their conversion into sustainable building materials through alkali activation.

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.

Morphology and thermal properties of clay/PMMA nanocomposites obtained by miniemulsion polymerization.

Miniemulsion polymerization was used as the synthetic method to produce clay/poly(methyl methacrylate) nanocomposites. Two kinds of interfacial interactions clay-polymer particle were observed by electron microscopy, one where the polymer particles are adhered on the surface of the larger fragments of clay, and another where nanometric fragments of clay are encapsulated by polymer particles. Variations in the glass transition temperature (T(g)) and thermomechanical properties of the matrix, as function of clay content, were observed. In particular, at the highest clay loading (1.0 wt%) depression of T(g) and thermomechanical properties were observed. The increased clay-polymer matrix interfacial area appears to be the conditioning factor that determines such behavior.