Fundamental and applied aspects of ICP-MS have been investigated to gain an increased
understanding of the technique and improve on its analytical capabilities.
Dissociation temperatures of polyatomic ions were calculated using a double-focusing sector
instrument, to obtain more reliable mass spectral data with controlled vapour introduction via a
Dreschel bottle to allow accurate calculation of the ingredients in the plasma. The equilibrium
temperature for the plasma, operated at 1280 W calculated using CO*, and as the
thermometric probes, was c.a. 5800 - 7400 K, while using ArO* and ArC* as the thermometric
probes the temperature calculated was c.a 2000 - 7000 K. Calculated dissociation temperatures
were used to elucidate the site of formation of these ions. Results confirmed that strongly bound
ions such as CO* and C2* were formed in the plasma whereas weakly bound ions such as ArO*
and ArC* were formed in the interface region due to gross deviation of the calculated
temperatures from those expected for a system in thermal equilibrium.
The use of helium gas in a hexapole collision cell Attenuated the signals of ArH* Ar*
ArO*, Arc*, ArCl* and Ara* allowing improved determination of ^^K*, *'Ca*, ^^e* ^^Cr*, ''As*
and ^°Se*in standard solutions. The use of the hexapole collision cell also resulted in an
enhancement of analyte signals due to the thermalisation of the ion beam.
The ion kinetic energy of ions sampled from the plasma and those sampled from the
skimmer cone were determined using a modified lens stack to assess the significance for
memory effects of material deposited on the skimmer cone. The most probable kinetic energy of
Be* ions sampled from the skimmer cone was found to be 2A eV, which was considerably
lower than the most probable kinetic energy of Be* ions sampled from the plasma, which was
found to be 9.5 eV. The low kinetic energy of the ions deposited on the skimmer cone means
they will only contribute to the analytical signal under certain instrumental operating conditions.
The feasibility of liquid sample introduction into a LP-ICP-MS system designed for
gaseous sample introduction was investigated using a particle beam separator. The low signal
was attributed to the low gas kinetic temperature of the plasma which was confirmed by the fact
that the signal increased rapidly with increasing temperature of the transfer line between the
particle beam separator and the LP-ICP torch. This was also supported by the fact that more
volatile compounds gave mass spectra whereas less volatile compounds did not. A limit of
detection of 30 mg 1'^ for chlorobenzene was achieved.
Finally, silicon and phosphorus speciation was performed by HPLC coupled to sectorfield
ICP-MS. Silicones ranging in molecular weight from 162 g mol'^ - 16500 g mol"^ were
extracted from spiked human plasma and separated by size exclusion chromatography. Limits of
detection ranged from 12 ng ml"' Si* for the 162 gmol'^ silicone to 30 ng ml'' Si* for the 16500 g
mol' silicone. Organophosphate pesticides were extracted from spiked plasma and separated by
reversed phase chromatography. Recoveries were between 55 - 81 %. Limits of detection were
0.9 ng ml'' P* 1.8 ng ml'' P* 1.6 ng ml"' P* and 3.0 ng ml'' P* for dichlorvos, methyl parathion,
malathion and quinolphos respectively. Phosphates were extracted from various food products
and separated by ion-exchange chromatography. Limits of detection were 1.0 ng ml"' P* 2.3 ng
ml"' P*, and 39 ng ml"' P* for P04^", PaOy"^ and PsOio^" respectively.
Date of Award | 2002 |
---|
Original language | English |
---|
Awarding Institution | |
---|
Supervisor | E. Hywel Evans (Other Supervisor) |
---|
FUNDAMENTAL AND APPLIED MEASUREMENTS IN ICP-MS
CARTER, J. R. (Author). 2002
Student thesis: PhD