dc.description.abstract |
In this work, Laser-Induced Breakdown Spectroscopic Technique was applied for
detection of heavy metals and other contaminants in solid and liquid samples. This
technique was applied for qualitative as well as quantitative measurement of elemental
concentration present in test samples. A special chamber was designed and fabricated for
analysis of solid samples in which provisions were made for insertion of sample, its
rotation, evacuation, and introduction of various gases at different pressures. The LIBS
system was calibrated and applied for determination of contaminants present in the
samples in the pellet forms. Then the system was applied for sample collected from sites
such as crude oil waste dump, greenhouse soil, oil spilled contaminated site, mine ore
waste, iron slag, and chromium contaminated site from different locations of Saudi
Arabia. The role of various binding material in the LIBS performance for trace elemental
analysis of powder samples was also investigated.
The influence of ambient environment such as pressure, temperature, nature of
buffer gas on emission feature of solid sample was studied as well. Prior to LIBS
application to the actual samples, the important parameters influencing LIBS
performance were optimized. In this regard the effect of laser energy, distance between
fiber optics and target material, limit of detection, precision, accuracy, repeatability,
delay time were optimized. The concentrations detected with our LIBS system were
verified by the conventional method such as ICP and the relative accuracy of the system
for various elements was compared and found in the range of 0.03 - 0.6 at 2.5 % error
confidence. Most of the elements under investigation showed maximum signal intensity
at delay time between 4.0 and 5.5 μs and laser pulse energy between 20 mJ to 140 mJ.
Prior to application of LIBS the plasma parameters such as temperature and electron
density were also measured as these parameters play vital role in the sensitivity of LIBS
system. The plasma temperature for iron slag sample was estimated using Boltzman plot
of LIBS intensity for neutral iron lines and Stark broadening. The maximum plasma
temperature and electron densities at 40 mJ energy was 5554 K and 1.46 x 1016 cm-3,
respectively for these samples.
In order to analyze the liquid samples different setups were developed and tested.
The aim of fabricating the setup for liquid samples analysis was to keep the LIBS system
simple, and to improve accuracy & limit of detection of elements under investigation.
Calibration curves for metals of interest were drawn from standard solution of these
metals in distilled water. Later, the system was applied for quantitative detection of
contaminants in wastewater samples collected from paint industry, syringe manufacturing
industry and dairy plant. The results obtained with our LIBS setup were comparable with
that obtained from ICP. The experience gained through this work can be useful for the
development of a portable LIBS system for on-line analysis of contaminated sites with
heavy metals for improvement of the environment and controlling the pollution at
industrial sites. |
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