CARACTERIZACIÓN DE LÁSERS DE BAJA POTENCIA PARA UN SISTEMA DE GRABADO

En este trabajo se realiza la caracterización de un diodo láser que emite en la longitud de onda de 405 nm con potencias de emisión de 150 y 200 mW. El láser es integrado en una máquina CNC de dos grados de libertad, diseñada para analizar el grabado en diferentes materiales. Se obtienen los principales parámetros del diodo láser tales como: corriente de polarización, potencia óptica, corriente de umbral, espectro de emisión y punto focal. Al integrar el diodo láser en el sistema de posición xy, se caracteriza la velocidad y el ancho de la línea de grabado sobre diferentes materiales obteniendo resultados satisfactorios

Sol–Gel and Electrospinning Synthesis of Silica–Hydroxyapatite–Silver Nanofibers for SEIRAS and SERS

Surface-enhanced Raman spectroscopy (SERS) and Surface-enhanced infrared absorption spectroscopy (SEIRAS) are both novel techniques favored by the excitation of surface plasmons onto metal nanostructures. The light emitted from the metal surface couples with the vibrational transitions of molecules in proximity, enhancing its spectral response and leading to more sensitive and effective spectroscopic analysis. The absence of inexpensive and reproducible substrates is among the major impediments to the accurate implementation and optimal performance of the technique. The development of a low-cost active substrate based on silica–hydroxyapatite through sol–gel synthesis and electrospinning is addressed in the present study. Fibers of 512 ± 199 nm diameter were produced after sintering at 1150 °C on the electrospun mats. The fibers are fixed to an indium tin oxide (ITO) glass base for electrodeposition with 10 and 20 mM AgNO3 at 1.5 and 3.3 V at different time periods. Electrodeposition produced silver nanorods and nanocubes on the fibers. The SERS and SEIRAS activity of each one of the nine supports was tested using pyridine 1 nM, comparing it with the spectrum of pyridine 1 mM. An enhancement factor of 2.01 × 106 for the band at 3335 cm−1 was obtained during a SEIRAS essay for the support doped for 2 min at 3.3 V with 10 mM silver nitrate solution. The highest SERS enhancement factor was 3.46 × 108, for the band at 1567 cm−1 in the substrate doped for 5 min at 1.5 V with silver nitrate solution at 10 mM. After testing both samples with 10−4 M violet crystal solution, no SERS enhancement factor was found, but higher band resolution in the spectra was observed

Sol-Gel and Electrospinning Synthesis of Lithium Niobate-Silica Nanofibers

Lithium niobate-silica fibers were produced by the combination of the sol-gel method and the electrospinning technique. Two sol-gel solutions starting from niobium-lithium ethoxide and tetraethyl orthosilicate were prepared and then mixed with polyvinylpyrrolidone; the solutions were electrospun in a coaxial setup. The obtained lithium niobate-silica polymeric fibers were approximately 760 nm in diameter. Raman spectroscopy confirmed the composite composition by showing signals corresponding to lithium niobate and silica. Scanning electron microscopy showed coaxial fibers with a diameter of around 330 nm arranged as a fibrillar membrane at 800 °C. At 1000 °C the continuous shape of fibers was preserved; the structure is composed of silica and lithium niobate nanoparticles within the fibers. The formation of crystalline lithium niobate and amorphous SiO2 phase was also confirmed by XRD peaks

Surface Enhanced Infrared Absorption Studies of SiO2–TiO2–Ag Nanofibers: Effect of Silver Electrodeposition Time on the Amplification of Signals

Surface Enhanced on Infrared Absorption (SEIRAS) and Raman Spectroscopy (SERS) are nondestructive analytic techniques used to detect low concentrations and recognize the fingerprints of molecules. The recognition of the absorption from samples by conventional infrared spectroscopy (IR) via Attenuated Total Reflection (ATR) is difficult for molecules with a low signal strength. However, developed structures with SERS and SEIRAS effect present problems such as high cost, low stability, and low compatibility. Research into new media to obtain greater amplification is largely based on the creation of nanoscale structures with symmetrical arrangements and reproducible distances, resulting in aggregates of nanoparticles that help generate hot spots which are active for amplification. The sol-gel and electrospinning method for the obtention of ceramics provides an alternative means by which to produce said substrates. Fibers of nanometric scale provide an increase of surface area which allows more contact to occur with analytes. Consequently, in this study, a silica-titania-silver nanostructured support that amplifies signal intensity for Raman and infrared spectroscopy was developed. The silica-titania support was developed by sol-gel and electrospinning techniques, and the as spun fibers were treated at 800 °C. Then, the ceramic fibrous membrane was placed on conductive indium tin oxide plastic to be doped with silver using an electroplating technique, varying the silver nitrate concentration (5, 10 and 20 mM), as well as electrodeposition times (1, 2, 5 and 10 min), with a constant voltage (1 V). Twelve different supports were obtained that showed amplification. The enhancement of infrared signals from pyridine and crystal violet molecules adsorbed on silica-titania-silver (SiO2–TiO2–Ag) nanofibers was studied in situ by Attenuated Total Reflection-Fourier Transformed Infrared Spectroscopy (ATR-FTIR). The highest amplification was obtained by the support doped at 10 min in a 10 mM concentration, with an amplification factor of 2.74 in the band localized at 3301 cm−1. In Raman spectroscopy, the highest amplification factor was 27.03, on the support doped for 5 min at a concentration of 5 mM

Thickness Effect on the Solvent Sensing Parameters of Carbon Black-polymer Composites

AbstractStudy of the sensing parameters: sensibility, response and recuperation times to hexane vapors for layers of different thickness of poly(butadiene) + carbon black (CB) composites is presented. The results show that sensibility increases as the CB- weight percent diminishes, being in agreement with reported results by several researches. In this work another variable was studied on the sensing parameters, the thickness. The initial electrical resistance of the studied layers increases until three magnitude orders as diminish theirs thickness and the sensibility in this study increases until one magnitude order as the layer thickness diminishes around 0.25μm

Structural and Magnetic Behavior of Oxidized and Reduced Fe Doped LiNbO3 Powders

Changes in structural and magnetic properties have been systematically induced in lithium niobate (LiNbO3) powders, Fe-doped with different concentrations and thermally treated in oxidized and reduced states. A rather strong ferromagnetic response at room temperature with a saturation magnetization of 0.96 Am2kg−1 was obtained for the higher utilized doping concentration, which is of the order of 1% mol. This may be considered a first report of the manifestation of ferromagnetism in nanocrystalline lithium niobate powders within the regime of very low Fe-doping concentrations. Post-thermal treatment in a controlled atmosphere is key for inducing and detecting this behavior, which can also be explained as the effective recombination of Fe impurities with oxygen vacancies in the surface of the material. Mechanochemical-calcination was employed for the synthesis of LiNbO3 powders and after that, a diffusion process of 0.44%, 0.89%, 1.47% and 2.20% mass of Fe2O3 was used in the Fe-doping. Oxidation and reduction processes were performed using a controlled atmosphere of ultra-high purity oxygen and hydrogen, respectively. X-ray diffraction and Raman spectroscopy were employed to characterize the materials. The magnetic properties were studied using Vibration Sample magnetometry and Electron Spin Resonance spectroscopy

Structural and Magnetic Behavior of Oxidized and Reduced Fe Doped LiNbO3 Powders

Changes in structural and magnetic properties have been systematically induced in lithium niobate (LiNbO 3) powders, Fe-doped with different concentrations and thermally treated in oxidized and reduced states. A rather strong ferromagnetic response at room temperature with a saturation magnetization of 0.96 Am 2 kg− 1 was obtained for the higher utilized doping concentration, which is of the order of 1% mol. This may be considered a first report of the manifestation of ferromagnetism in nanocrystalline lithium niobate powders within the regime of very low Fe-doping concentrations. Post-thermal treatment in a controlled atmosphere is key for inducing and detecting this behavior, which can also be explained as the effective recombination of Fe impurities with oxygen vacancies in the surface of the material. Mechanochemical-calcination was employed for the synthesis of LiNbO 3 powders and after that, a diffusion process of 0.44%, 0.89%, 1.47% and 2.20% mass of Fe 2 O 3 was used in the Fe-doping. Oxidation and reduction processes were performed using a controlled atmosphere of ultra-high purity oxygen and hydrogen, respectively. X-ray diffraction and Raman spectroscopy were employed to characterize the materials. The magnetic properties were studied using Vibration Sample magnetometry and Electron Spin Resonance spectroscopy