激光诱导击穿光谱
分析化学(期刊)
光谱学
色散(光学)
谱线
土工试验
材料科学
原子发射光谱法
激光器
电离
化学
土壤水分
等离子体
环境科学
环境化学
光学
土壤科学
离子
感应耦合等离子体
物理
天文
量子力学
有机化学
作者
Nick Glumac,Willie K. Dong,W. M. Jarrell
标识
DOI:10.2136/sssaj2010.0100
摘要
Standard laser‐induced breakdown spectroscopy (LIBS) offers a potentially rapid, accurate, field‐portable, and low‐cost technique for the measurement of C content in soil samples. Neutral and singly ionized Fe lines form significant interferences, however, that can compromise the LIBS C measurement. In this study, the 247.8‐nm line of atomic C (C I) was examined in detail to assess the effect of potential elemental interferences. These interferences and their spectral and temporal signatures were evaluated using control graphite and Fe oxide samples. A combination of high dispersion and appropriate time gating of the LIBS signal was found to generate very high signal/noise ratio spectra using low laser powers and therefore, allowed accurate determination of the C content down to the subpercent level in the presence of Fe interferences. Although the contribution of one singly ionized Fe line cannot be entirely eliminated, a method to quantitatively assess the contribution of this line was developed. The new technique was tested on soil samples with organic C content in the 0.5 to 3% (w/w) range, and a strong correlation of the LIBS C signal with measurements made by the thermal oxidation, dry combustion method was observed. The findings reaffirm the utility of standard LIBS for rapid and accurate laboratory measurement of soil C and the potential use of standard LIBS with further study and development for assessing soil C in situ.
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