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A neutral particle analyzer is used to measure the time-resolved energy spectrum of neutral hydrogen leaving a spheromak plasma. A gas cell filled with 10-50 mTorr of helium is used to strip electrons from incoming neutral hydrogen, lowering the minimum detectable energy well below that obtained with thin foils. Effective neutral particle temperature is calculated by fitting a Maxwellian energy distribution to the measured energy spectrum above and below approximately 300 eV. A computational model with approximated profiles of plasma density and neutral density is used with the measured neutral hydrogen flux to estimate the ion temperature. Measurement of the power flux due to neutral hydrogen emitted at the measurement location is extended to the whole plasma surface to estimate the total charge exchange power loss from the plasma. The initial results indicate that the charge exchange power loss represents only 2% of the total input gun power during the sustainment phase of the discharge.

The flip-over effect in self-similar laser-induced plasma expansion Development of the megahertz planar laser-induced fluorescence diagnostic for plasma turbulence visualization Rev. Sci. Instrum. 75, 4115 (2004); 10.1063/1.1787148 A technique for temperature mapping in fluorocarbon plasmas using planar laser-induced fluorescence of CF By focusing a pulsed single mode Nd:YAG laser, we created low temperature plasmas at various pressures with various target gases and collected spectral light emissions to investigate the possibility of turbulent behavior in these types of plasmas. Characteristic fluctuation frequencies, chaotic dimensions, spectral indices, and turbulent fluctuation energies are determined from fluctuations in these spectral light emissions. Values calculated for the spectral index and the chaotic index for each plasma event are found to be within the known values for other turbulent plasma systems. Thus, turbulent fluctuations on a nanosecond time scale are confirmed in the time evolutions of various singly ionized and neutral spectral lines of various gases.

We detect thin films of 2,4,6-trinitrotoluene (TNT) and hexahydro-1,3,5-hexanitro-1,3,5-triazine (RDX) by one- and two-laser photofragmentation-fragment detection spectroscopy in real time at ambient temperature and pressure. In the one-laser technique, a laser tuned to 226 nm excites the energetic material and both generates the characteristic NO photofragments and facilitates their detection by resonance-enhanced multiphoton ionization (REMPI) using their A-X (0,0) transitions near 226 nm. In contrast, in the two-laser technique, a 454 nm laser generates the analyte molecule in the gas phase by matrix-assisted desorption, and a second laser tuned to 226 nm both photofragments it and ionizes the resulting NO. We report the effects of laser energy, analyte concentration, and matrix concentration on the ion signal and determine the rotational temperatures of the NO photofragments from Boltzmann, rotational distribution analysis of the REMPI spectra. We achieve limits of detection (S/N = 3) of hundreds of ng/cm(2) for both techniques under ambient conditions with a positive signal identification as low as 70 pg using a single 226 nm laser pulse of approximately 50 microJ.

Trace chemical detection is a particularly challenging problem of significant Army interest. Optical diagnostic techniques offer rapid, accurate, sensitive, and highly selective detection of hazardous materials in a variety of systems. Multiplex coherent anti-stokes Raman scattering (MCARS) spectroscopy generates a complete Raman spectrum from the material of interest using a combination of a supercontinuum pulse, which drives multiple molecular vibrations simultaneously, and a narrowband probe pulse. In this study, we demonstrated the ability of MCARS to detect trace amounts of both explosive materials and chemical warfare agent simulants with limits of detection below 0.2 ng and 0.1 nl, respectively. Integration times were on the order of 10 ms, using a compact USB spectrometer. Characteristics of supercontinuum generation were studied and compared to results in the literature. Finally, an algorithm that utilizes a combination of the maximum entropy method and advanced Fourier filtering to analytically remove the non-resonant background from the MCARS spectra without any a priori knowledge of the vibrational spectrum of the material of interest.

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