Identifying and implementing techniques for carbon management has become an important endeavor in the mitigation of global climate change. Two important techniques being pursued are geologic and terrestrial carbon sequestration. With regard to terrestrial sequestration, in order to accurately monitor changes in soil carbon potentially induced by sequestration practices, rapid, cost-effective, and accurate measurements must be developed. Spark-induced breakdown spectroscopy (SIBS) has the potential to be used as a field-deployable method to monitor changes in the concentration of carbon in soil. SIBS spectra in the 248 nm region of eight soils were collected, and the neutral carbon line at 247.85 nm was compared to total carbon concentration determined by standard dry combustion techniques. Additionally, Fe and Si emission lines were evaluated in a multivariate statistical model to evaluate their impacts on the model's predictive power for total carbon concentrations. The preliminary results indicate that SIBS is a viable method to quantify total carbon levels in soils, obtaining a correlation of (R(2)=0.972) between measured and predicated carbon in soils. These results show that multivariate analysis can be used to construct a calibration model for SIBS soil spectra.
Public reporting burden for the collection of information is estimated to average 1 hour per response, including the time for reviewing instructions, searching existing data sources, gathering and maintaining the data needed, and completing and reviewing the collection of information. )] produced by this reaction. Upon addition of HI to the flow, the reaction of H + HI produced iodine atoms that were pumped to the excited I( 2 P 1/2 ) state, and we observed strong emission from the I atom 2 P 1/2 -> 2 P 3/2 transition at 1.315 µm. With a tunable diode laser we probed the I atom transition and observed significant transfer of population from ground state ( 2 P 3/2 ) to the excited state ( 2 P 1/2 ) and have observed optical transparency within the iodine atom energy level manifold.
The goal of this review article is to provide a description of recent and novel laser-induced breakdown spectroscopy (LIBS) applications and developments, especially those discussed during the NASLIBS Conference, held during SciX in Providence, RI, in September 2015. This topic was selected in view of the numerous recent overall review papers that have successfully given a broad view of the current understanding of laser-material interactions and plasma development and have also discussed the wide landscape of analytical applications of LIBS. This paper is divided into sections that focus on a few of the many applications under development in the LIBS community. We provide a summary of updates to calibrationfree LIBS (CF-LIBS) and associated developments using plasma characteristics to improve quantification in LIBS output, both in a dedicated section and as applications are discussed. We have also described the most recent publications studying the sources, generation, and use of molecular features in LIBS, including those naturally present in the spectra of organic materials, and those induced with the addition of salts to enable the measurement of halogens, not typically present in LIBS signals. In terms of development of applications of LIBS, we focused on the use of LIBS for indirect measurements such as pH and degree of humification in soil and heating value in coal. We also reviewed the extant literature on LIBS analysis of agricultural materials, coal, minerals, and metals. Finally, we discuss the nascent developments of spatially heterodyne spectroscopy, a method that seeks to circumnavigate a serious drawback of most spectrometers -very small optical throughput -through the use of interferometers.
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