2,441 research outputs found

    Remote Raman detection of chlorine with deep UV excitation wavelengths

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    Deep ultraviolet Raman spectroscopy measurements have been performed at the German Aerospace Center (DLR) to detect chlorine gas. In this study a remote Raman set up was optimized to detect chlorine gas at a distance of 60 cm. Several ultraviolet laser wavelengths (224, 232, 235 nm respectively, 2.5 mJ/pulse at 10 Hz) were changed to experimentally observe the highest possible signal to noise ratio. For each tested excitation wavelength, chlorine spectra were successfully detected. Detection limits in acquisition times for a 0.36 bar chlorine sample are discussed. A possible solution to avoid spectral overlapping of the background material with the sample is presented

    Dual-pump CARS of Air in a Heated Pressure Vessel up to 55 Bar and 1300 K

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    Dual-pump Coherent anti-Stokes Raman scattering (CARS) measurements have been performed in a heated pressure vessel at NASA Langley Research Center. Each measurement, consisting of 500 single shot spectra, was recorded at a fixed location in dry air at various pressures and temperatures, in a range of 0.03-5510(exp 5) Pa and 300-1373 K, where the temperature was varied using an electric heater. The maximum output power of the electric heater limited the combinations of pressures and temperatures that could be obtained. Charts of CARS signal versus temperature (at constant pressure) and signal versus pressure (at constant temperature) are presented and fit with an empirical model to validate the range of capability of the dual-pump CARS technique; averaged spectra at different conditions of pressure and temperature are also shown

    RDX Remote Raman Detection on NATO SET-237 Samples

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    Ultraviolet Raman spectroscopy measurements have been performed at DLR Lampoldshausen to detect NATO SET-237 standard samples of RDX. The main goal was to quantify the minimum requirements for an unambiguous identification in remote detection (60 cm distance) with a commercial Czerny-Turner spectrometer coupled with a CCD camera. Well-defined distribution of explosives on surfaces were tested as standardized samples. Therefore, Raman spectra of RDX have been acquired for different sample concentrations (50, 250, and 1000 μg/cm2 respectively) and under several laser energies (1.5, 3.0 and 5.0 mJ/pulse respectively) at 355 nm excitation wavelength. The lowest possible reproducible surface concentration (50 µg/cm2) was detected with excitation energy of 3 mJ/pulse in the described configuration

    EDX Remote Detection on NATO SET-237 Samples

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    Ultraviolet Raman spectroscopy measurements have been performed at DLR Lampoldshausen to detect NATO SET-237 standard samples of RDX. The goal was to quantify the minimum requirements for an unambiguous identification in remote detection (60 cm distance) arrangement using simple and robust spectroscopic equipment on well-defined distribution of explosives on surfaces. Therefore, Raman spectra of RDX have been acquired for different sample concentrations (50, 250, and 1000 μg/cm2 respectively) and under several laser energies (1.5, 3.0 and 5.0 mJ/pulse respectively) at 355 nm excitation wavelength. The lowest producible surface concentration (50 µg/cm2) was detected with excitation energy of 3 mJ/pulse in the described configuration. The presented Raman spectra are also discussed in terms of future applications

    Remote Raman Spectroscopy of Explosive Precursors

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    Deep ultraviolet Raman spectroscopy measurements have been performed at the German Aerospace Center (DLR) with the aim of detecting traces (µg range) of explosive precursors. In this study a backscattering Raman system was set up and optimized to detect urea, sodium perchlorate, ammonium nitrate, and sodium nitrate at a 60 cm short-range remote detection. Sample were tested at 264 nm ultraviolet laser excitation wavelength to experimentally observe any possible trace over textiles samples. For each colored sample textile, Raman spectra were acquired and no background fluorescence interference was observed at this laser excitation wavelength. Detection limits and system sensitivity with an acquisition times up to 3 seconds for microgram traces are presented

    Dual-Pump CARS Measurements in the University of Virginia's Dual-Mode Scramjet: Configuration "A"

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    In this paper we describe efforts to obtain canonical data sets to assist computational modelers in their development of models for the prediction of mixing and combustion in scramjet combustors operating in the ramjet-scramjet transition regime. The CARS technique is employed to acquire temporally and spatially resolved measurements of temperature and species mole-fraction at four planes, one upstream of an H2 fuel injector and three downstream. The technique is described and results are presented for cases with and without chemical reaction. The vibrational energy mode in the heated airstream of the combustor was observed to be frozen at near facility heater conditions and significant nonuniformities in temperature were observed, attributed to nonuniformities of temperature exiting the heater. The measurements downstream of fuel injection show development of mixing and combustion, and are already proving useful to the modelers

    Dual-Pump CARS Measurements in the University of Virginia's Dual-Mode Scramjet: Configuration "C"

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    Measurements have been conducted at the University of Virginia Supersonic Combustion Facility in configuration C of the dual-mode scramjet. This is a continuation of previously published works on configuration A. The scramjet is hydrogen fueled and operated at two equivalence ratios, one representative of the scram mode and the other of the ram mode. Dual-pump CARS was used to acquire the mole fractions of the major species as well as the rotational and vibrational temperatures of N2. Developments in methods and uncertainties in fitting CARS spectra for vibrational temperature are discussed. Mean quantities and the standard deviation of the turbulent fluctuations at multiple planes in the flow path are presented. In the scram case the combustion of fuel is completed before the end of the measurement domain, while for the ram case the measurement domain extends into the region where the flow is accelerating and combustion is almost completed. Higher vibrational than rotational temperature is observed in those parts of the hot combustion plume where there is substantial H2 (and hence chemical reaction) present

    Use of natural clays as sorbent materials for rare earth ions: materials characterization and set up of the operative parameters

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    Two mineral clays of the montmorillonite group were tested as sorbents for the removal of Rare Earths (REs) from liquid solutions. Lanthanum and neodymium model solutions were used to perform uptake tests in order to: (a) verify the clays sorption capability, (b) investigate the sorption mechanisms and (c) optimize the experimental parameters, such as contact time and pH. The desorption was also studied, in order to evaluate the feasibility of REs recovery from waters. The adsorption–desorption procedure with the optimized parameters was also tested on a leaching solution obtained by dissolution of a dismantled NdFeB magnet of a hard-disk. The clays were fully characterized after REs adsorption and desorption by means of X-ray powder diffraction (XRPD) and X-ray photoelectron spectroscopy (XPS); the liquid phase was characterized via Inductively Coupled Plasma–Optical Emission Spectroscopy (ICP–OES) analyses. The experimental results show that both clays are able to capture and release La and Nd ions, with an ion exchange mechanism. The best total efficiency (capture 50%, release 70%) is obtained when the uptake and release processes are performed at pH = 5 and pH = 1 respectively; in real leached scrap solutions, the uptake is around 40% but release efficiency is strongly decreased passing from a mono-ion system to a real system (from 80% to 5%). Furthermore, a strong matrix effect is found, with the matrix largely affecting both the uptake and the release of neodymium
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