The three electrode direct current plasma (DCP), has been investigated
for the analysis of samples introduced using aqueous solution nebulisation, hydride generation and slurry atomisation. For aqueous solutions,
simplex optimisation with signal to background ratio as the criterion
of merit, vertical viewing position was found to be most critical.
A continuous-flow hydride generator was interfaced to the DCP via a
modified sample introduction chimney. Optimisation indicated that total
sample introduction gas flow rates were essentially similar to those
for conventional nebulisation and that vertical viewing position was
again critical. Generation conditions for lead hydride were also simplex
optimised. Acid, sodium hydroxide, and hydrogen peroxide concentration
were all found to be critical. Detection limits for hydride generation
were: As 4 ng cmˉ³, Se 4 ng cmˉ³, Pb 10 ng cmˉ³. Arsenic and selenium
were accurately determined in various reference materials.
The determination of Mg in aqueous slurries of kaolin was optimised
using the Mg(II) 279.079 nm line and conventional sample introduction.
Vertical viewing position was again critical with the optimum on the
boundary of the analytical zone and over the plasma core. A reduction
of emission intensity at high slurry concentrations (> 12%), was
observed.
Particle size was the most important parameter in slurry atomisation,
< 5 µm being preferred. Soils, milk, plant materials and sewage sludges
were successfully analysed by slurry atomisation. Where necessary,
particle size was reduced using simple grinding procedures. For fibrous
materials, prior matrix carbonisation was advantageous. Results obtained
using these procedures and simple aqueous calibration showed excellent
agreement with certified values of reference materials.
Electron number density (ne), excitation temperature (Texc) and ionisation
temperature (Tion), were measured for two series of kaolin slurries,
(1-20% m/V), one containing 5 g 1ˉ¹ lithium as enhancement buffer. For
the slurries containing added lithium, Texc and ne were found to be
reduced with increasing slurry concentration. Observed decreases in
analyte emission with increased sample loadings (> 12%), are considered to
be consistent with proposed excitation models.
Date of Award | 1986 |
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Original language | English |
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Awarding Institution | |
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AGRICULTURAL ANALYSIS BY PLASMA EMISSION SPECTROSCOPY WITH SLURRY ATOMISATION
SPARKES, S. T. (Author). 1986
Student thesis: PhD