RESUMEN
Molecular gases are highly relevant in healthcare, production control, safety, and environmental monitoring. They often appear in small concentrations. The measurement of trace gases has increasingly become a key technique in those domains. Quartz-enhanced photoacoustic spectroscopy (QEPAS) is a suitable method that can provide the required low detection limits in such applications at comparatively low cost and small size. For mobile implementation, the size of an entire sensor unit matters. In this paper, we present a QEPAS sensor that fits into a standard butterfly package, its characterization, and its application on CH4 and CO2.
Asunto(s)
Contaminantes Atmosféricos/análisis , Técnicas Biosensibles/instrumentación , Dióxido de Carbono/análisis , Metano/análisis , Técnicas Fotoacústicas/instrumentación , Cuarzo/química , Análisis Espectral/métodos , Monitoreo del Ambiente/métodos , Diseño de EquipoRESUMEN
The rapid detection of trace gases is of great relevance for various spectroscopy applications. In this regard, the technology of external cavity diode lasers (ECDLs) has firmly established itself due to its excellent properties. Outside of the laboratory environment, however, these still have some restrictions, especially with regard to high acquisition rates for sensitive spectroscopy applications and mode-hop-free tuning. In this article, we present our innovative GaSb-based ECDL concept, in which a resonantly driven microelectromechanical system actuator is used. With this, a defined frequency range can be tuned extremely fast and without mode hops. Results of the characterization and its use for the rapid detection of trace gases are presented.
RESUMEN
The MIR wavelength regime promises better gas detection possibilities than the NIR or the visible region because of the higher absorbencies simulated by HITRAN. In the MIR region are many important absorption lines of significant gases, which are relevant in healthcare, production supervision, and safety and environmental monitoring. One of those gases is methane. CH4 shows significant variations in absorbance with a maximum at 3.3 µm, which results in low detection limits in the range of low ppm. Interband-cascade- and quantum-cascade-based lasers emit at higher wavelengths, where the absorbencies of methane are higher. The comparison is done by analyzing the performance of two spectroscopy applications: tunable diode laser absorption spectroscopy and quartz-enhanced photoacoustic spectroscopy.
RESUMEN
The measurement of trace gases has increasingly become a key technique in healthcare and other medical applications. Quartz-enhanced photoacoustic spectroscopy (QEPAS) is a suitable method that can provide the required characteristics in such applications for a comparatively low cost and small size. The quantitative detection and a low detection limit are also required by applications. In this paper, we present new results on sensing biomedically relevant gases using the on-beam QEPAS technique with some newly developed tunable high-power single-mode laser diodes based on GaSb material. The data processing and detection limit determination are done by a field programmable gate array device, as well as an automatic measurement of the resonance frequency.
RESUMEN
The wavelength, λ, range of 1.8 µm≤λ≤3.5 µm contains strong spectral absorption lines of many gases used in health, industry, safety, and medicine and whose sensitive and quantitative detection is desirable. However, the performance of InP diode lasers markedly deteriorates beyond λâ¼2 µm. In this paper we present new results on developing tunable high power single mode laser diodes based on the GaSb material system with emission in the wavelength range of 1.8 µm≤λ≤2.2 µm.
RESUMEN
The manufacture of 3D scaffolds with specific controlled porous architecture, defined microstructure and an adjustable degradation profile was achieved using two-photon polymerization (TPP) with a size of 2 × 4 × 2 mm(3). Scaffolds made from poly(D,L-lactide-co-É-caprolactone) copolymer with varying lactic acid (LA) and É -caprolactone (CL) ratios (LC16:4, 18:2 and 9:1) were generated via ring-opening-polymerization and photoactivation. The reactivity was quantified using photo-DSC, yielding a double bond conversion ranging from 70% to 90%. The pore sizes for all LC scaffolds were see 300 µm and throat sizes varied from 152 to 177 µm. In vitro degradation was conducted at different temperatures; 37, 50 and 65 °C. Change in compressive properties immersed at 37 °C over time was also measured. Variations in thermal, degradation and mechanical properties of the LC scaffolds were related to the LA/CL ratio. Scaffold LC16:4 showed significantly lower glass transition temperature (T g) (4.8 °C) in comparison with the LC 18:2 and 9:1 (see 32 °C). Rates of mass loss for the LC16:4 scaffolds at all temperatures were significantly lower than that for LC18:2 and 9:1. The degradation activation energies for scaffold materials ranged from 82.7 to 94.9 kJ mol(-1). A prediction for degradation time was applied through a correlation between long-term degradation studies at 37 °C and short-term studies at elevated temperatures (50 and 65 °C) using the half-life of mass loss (Time (M1/2)) parameter. However, the initial compressive moduli for LC18:2 and 9:1 scaffolds were 7 to 14 times higher than LC16:4 (see 0.27) which was suggested to be due to its higher CL content (20%). All scaffolds showed a gradual loss in their compressive strength and modulus over time as a result of progressive mass loss over time. The manufacturing process utilized and the scaffolds produced have potential for use in tissue engineering and regenerative medicine applications.