Green synthesis of ZnO nanoparticles from ball moss (Tillandsia recurvata) extracts: characterization and evaluation of their photocatalytic activity.

Green synthesis (GS), referred to the synthesis using bioactive agents such as plant materials, microorganisms, and various biowastes, prioritizing environmental sustainability, has become increasingly relevant in international scientific practice. The availability of plant resources expands the scope of new exploration opportunities, including the evaluation of new sources of organic extracts, for instance, to the best of our knowledge, no scientific articles have reported the synthesis of zinc oxide nanoparticles (ZnO NPs) from organic extracts of T. recurvata, a parasitic plant very common in semiarid regions of Mexico.This paper presents a greener and more efficient method for synthesizing ZnO NPs using T. recurvata extract as a reducing agent. The nanoparticles were examined by different techniques such as UV-vis spectroscopy, X-ray diffraction, scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and BET surface analysis. The photocatalytic and adsorptive effect of ZnO NPs was investigated against methylene blue (MB) dye in aqueous media under sunlight irradiation considering an equilibrium time under dark conditions. ZnO nanoparticles were highly effective in removing MB under sunlight irradiation conditions, showing low toxicity towards human epithelial cells, making them promising candidates for a variety of applications. This attribute fosters the use of green synthesis techniques for addressing environmental issues.This study also includes the estimation of the supported electric field distributions of ZnO NPs in their individual spherical or rounded shapes and their randomly oriented organization, considering different diameters, by simulating their behavior in the visible wavelength range, observing resonant enhancements due to the strong light-matter interaction around the ZnO NPs boundaries.

Bone samples' behavior in sunlight, IR light, and temperature increase with FEM simulation.

Biological and environmental factors produce biochemical processes that modify the bone structure. A few studies have attempted to show the adverse biological effects of sun radiation. The bone tissue exposures to infrared and sunlight radiation are analyzed by using focused sound, characterization spectroscopy techniques, and image processing. The study is complemented with a finite element method simulation on temperature behaviors. The crystal morphology on the bone hydroxyapatite and functional groups was characterized by X-ray diffraction and infrared spectroscopy. The infrared spectra confirmed the hydroxyl group of bovine hydroxyapatite, amines, and lipids are also correlated with modifications of the hydroxyapatite. The diffractograms showed the characteristic peaks of hydroxyapatite, with the main intensity at 2θ = 32.02°. Bone samples exposed to sun radiation presented a peak at 2θ = 27.5°, evidencing the possible formation of ß-TCP y α-TCP. The analysis with the spectroscopy techniques about the structural changes in the samples suggests interpreting an increase of sound obtained by expanding the exposure time. It is possible to verify that there are some structural changes in the bone samples due to exposure to non-ionizing radiation. These results show an increase in the registered intensity sound correlated with the interpretation of the structural changes of bone. Thanks to the different novel analysis techniques established in the present study, it could establish the changes that experienced the bone structure under different sources of radiation, which will help to better detect scenarios of bone deficiency.

A novel and stretchable carbon-nanotube/Ni@TiO2:W photocatalytic composite for the complete removal of diclofenac drug from the drinking water.

We present the structural, morphological and photocatalytic properties of stretchable composites made with carbon nanotubes (CNTs), silicon rubber and Ni@TiO2:W nanoparticles (TiWNi NPs) with average size of 37 ± 2 nm. Microscopy images showed that the TiWNi NPs decorated the surface of the CNT fibers, which are oriented in a preferential direction. TiWNi NPs presented a mixture of anatase/rutile phases with cubic structure. The performance of the TiWNi powders and stretchable composites was evaluated for the photocatalytic degradation of diclofenac (DCF) anti-inflammatory drug under ultraviolet-visible light. The results revealed that the maximum DCF degradation percentages were 34.6%, 91.9%, 97.1%, 98.5% and 100% for the CNT composite (stretched at 0%), TiWNi powders, CNT + TiWNi (stretched at 0%), CNT + TiWNi (stretched at 50%) and CNT + TiWNi (stretched at 100%), respectively. Thus, stretching the CNT + TiWNi composites was a good strategy to enhance the DCF degradation percentage from 97.1% to 100%, since stretching created additional defects (oxygen vacancies) that acted as electron sink, delaying the electron-hole recombination, and favors the DCF degradation. Raman/absorbance measurements confirmed the presence of such defects. Moreover, the reactive oxygen species (ROS) were determined by the scavenger's experiments and found that the main ROS were the ·OH and O2- radicals, which attacked the DCF molecules, causing their degradation. The results of this investigation confirmed that the stretchable CNT/TiWNi-based composites are a viable alternative to remove pharmaceutical contaminants from water and can be manually separated from the decontaminated water, which is unviable using photocatalytic powders.

Fluorescent organic particle doped polymer-based gel dosimeter for neutron detection.

The purpose of this work is to develop a material capable of detecting neutrons produced by photodisintegration in a linear accelerator for its medical use. In this study, we have developed a gel-like material doped with fluorescent organic particles. PPO at 1 wt% is used as primary dopant and POPOP as secondary one at 0.03 wt%. A set of four samples is produced, with boric acid concentrations of 0, 400, 800 and 1200 ppm. The viscoelastic properties of the material are characterized with rheological measurements, finding a gel-like behavior, i.e., a material that can keep its original shape if no stresses are applied, but can also be deformed by applying a moderate shear rate. Furthermore, the material was irradiated with gamma, electron, and neutron emission sources from 137Cs, 22Na, 60Co, 210Po, 90Sr and 241AmBe, and its response was measured in two different experimental settings, in two different institutions, for comparative purposes. From these measurements, one can clearly establish that the new material detects neutrons, electrons, and gammas within the MeV regions and below. Thus, our findings show that the developed material and its properties make it a promising technology for its use in a neutron detector.

Nanoparticulate Double-Heterojunction Photocatalysts Comprising TiO2(Anatase)/WO3/TiO2(Rutile) with Enhanced Photocatalytic Activity toward the Degradation of Methyl Orange under Near-Ultraviolet and Visible Light.

Nanoparticulate double-heterojunction photocatalysts comprising TiO2(Anatase)/WO3/TiO2(Rutile) were produced by a sol-gel method. The resulting photocatalysts exhibit clear synergistic effects when tested toward the degradation of methyl orange under both UV and visible light. Kinetic studies indicate that the degradation rate on the best double-heterojunction photocatalyst (10 wt % WO3-TiO2) depends mainly on the amount of dye concentration, contrary to pure oxides in which the degradation rate is limited by diffusion-controlled processes. The synergistic effects were confirmed through systematic and careful studies including holes and OH radical formation, X-ray diffraction, electron microscopy, elemental analysis, UV-vis diffuse reflectance spectroscopy, and surface area analysis. Our results indicate that the successful formation of a double heterojunction in the TiO2(Anatase)/WO3/TiO2(Rutile) system leads to enhanced photoactivity when compared to individual oxides and commercial TiO2 P25.

MAl2O4 (M=Ba, Mg) photocatalytic activity dependence on annealing atmosphere.

Aluminate spinel type ${{\rm MAl}_2}{{\rm O}_4}$MAl2O4 (M=Ba or Mg) materials prepared using the combustion synthesis method were annealed either in an air or carbon atmosphere. The materials were characterized using X-ray diffraction, scanning electron microscopy, diffuse reflectance spectra, electrochemical impedance spectroscopy, and photoluminescence (PL) measurements. Their photocatalytic activity was evaluated for the dye degradation and hydrogen evolution. Methylene blue (15 ppm) was completely degraded using the air-annealed barium aluminate after 90 min, while a maximum hydrogen generation rate of $97 . 0 \;{\rm\unicode{x00B5}{\rm mol}\cdot{\rm h}^{ - 1}\cdot{\rm g}^{ - 1}}$97.0µmol⋅h-1⋅g-1 was achieved using the carbon-annealed magnesium aluminate. The results suggest that air-annealed photocatalysts are suitable for oxidation-dependent reactions, while carbon annealing may enhance reduction-dependent reactions.

Photodegradation of indigo carmine and methylene blue dyes in aqueous solution by SiC-TiO2 catalysts prepared by sol-gel.

Indigo carmine and methylene blue dyes in aqueous solution were photodegraded using SiC-TiO(2) catalysts prepared by sol-gel method. After thermal treatment at 450°C, SiC-TiO(2) catalysts prepared in this work showed the presence of SiC and TiO(2) anatase phase. Those compounds showed specific surface area values around 22-25 m(2)g(-1), and energy band gap values close to 3.05 eV. In comparison with TiO(2) (P25), SiC-TiO(2) catalysts showed the highest activity for indigo carmine and methylene blue degradation, but this activity cannot be attributed to the properties above mentioned. Therefore, photocatalytic performance is due to the synergy effect between SiC and TiO(2) particles caused by the sol-gel method used to prepare the SiC-TiO(2) catalysts. TiO(2) nanoparticles are well dispersed onto SiC surface allowing the transfer of electronic charges between SiC and TiO(2) semiconductors, which avoid the fast recombination of the electron-hole pair during the photocatalytic process.