With the use of laser-induced breakdown spectroscopy (LIBS), the effects of chemical speciation and matrix composition on Pb and Ba measurements have been investigated by using sand and soil matrices. A cylindrical lens was used to focus the laser pulses on the samples because it yielded higher measurement precision than a spherical lens for the experimental conditions used here. The detection limits for Pb and Ba spiked in a sand matrix were 17 and 76 ppm (w/w), respectively. In spiked soil, the detection limits were 57 and 42 ppm (w/w) for Pb and Ba, respectively. Measurement precision for five replicate measurements was typically 10% RSD or less. Two factors were found to influence emissions from Pb and Ba present in sand and soil matrices as crystalline compounds: (1) compound speciation, where Ba emission intensities varied in the order carbonate > oxide > sulfate > chloride > nitrate, and where Pb emission intensities varied in the order oxide > carbonate > chloride > sulfate > nitrate; and (2) the composition of the bulk sample matrix. Emissions from Ba(II) correlated inversely with the plasma electron density, which in turn was dependent upon the percent sand in a sand/soil mixture. The analytical results obtained here show that a field-screening instrument based on LIBS would be useful for the initial screening of soils contaminated with Pb and Ba.

We present validation and some applications of two laser-driven shock wave loading techniques: laser-launched flyer plate and confined laser ablation. We characterize the flyer plate during flight and the dynamically loaded target with temporally and spatially resolved diagnostics. With transient imaging displacement interferometry, we demonstrate that the planarity (bow and tilt) of the loading induced by a spatially shaped laser pulse is within 2-7 mrad (with an average of 4+/-1 mrad), similar to that in conventional techniques including gas gun loading. Plasma heating of target is negligible, in particular, when a plasma shield is adopted. For flyer plate loading, supported shock waves can be achieved. Temporal shaping of the drive pulse in confined laser ablation allows for flexible loading, e.g., quasi-isentropic, Taylor-wave, and off-Hugoniot loading. These techniques can be utilized to investigate such dynamic responses of materials as Hugoniot elastic limit, plasticity, spall, shock roughness, equation of state, phase transition, and metallurgical characteristics of shock-recovered samples.

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Two-photon polarization spectroscopy is an established method for making excited state symmetry assignments in randomly oriented samples. The relationship between the two-photon absorption process and the symmetry of the excited state, as established by previous theoretical developments, is illustrated in terms of the principles of the interaction between polarized light and oriented symmetric molecules. A description of the experimental methodology is presented and several applications for which this method has been used in vibronic coupling studies are discussed.

We have observed enhanced optical limiting behavior in solutions of a derivatized fullerene (phenyl-C(61)-butyric acid cholesteryl ester) from 532 to 700 nm. Transient absorption measurements determined the spectral and temporal regions of interest for optical limiting in C(60) and in C(60) derivatives that are due to a reverse saturable absorption mechanism and predicted enhanced limiting at longer wavelengths. Intensity-dependent transmission measurements made at several wavelengths confirmed these results. The increased solubility and the broadened ground-state absorption of the functionalized C(60) make it suitable for use as an optical limiter in the red and the near infrared.