USE OF MULTIPLE EMISSION-LINES AND PRINCIPAL COMPONENT REGRESSION FORQUANTITATIVE-ANALYSIS IN INDUCTIVELY-COUPLED PLASMA-ATOMIC EMISSION-SPECTROMETRY WITH CHARGE-COUPLED-DEVICE DETECTION

Citation
Da. Sadler et D. Littlejohn, USE OF MULTIPLE EMISSION-LINES AND PRINCIPAL COMPONENT REGRESSION FORQUANTITATIVE-ANALYSIS IN INDUCTIVELY-COUPLED PLASMA-ATOMIC EMISSION-SPECTROMETRY WITH CHARGE-COUPLED-DEVICE DETECTION, Journal of analytical atomic spectrometry, 11(11), 1996, pp. 1105-1112
Citations number
33
Categorie Soggetti
Spectroscopy
ISSN journal
02679477
Volume
11
Issue
11
Year of publication
1996
Pages
1105 - 1112
Database
ISI
SICI code
0267-9477(1996)11:11<1105:UOMEAP>2.0.ZU;2-I
Abstract
A procedure for the automatic selection of spectral lines, based upon principal component regression (PCR), is described, The procedure anal yses the consistency of the pattern of emission signals from a number of lines in both a series of standard solutions and the sample solutio n, From the calibration experiment the principal component associated with the largest eigenvalue is shown to be linearly dependent upon con centration and hence can be used to determine the unknown analyte conc entration in the sample solution, The detection limit for this princip al component is shown to be lower than the detection limit of any of t he individual spectral lines. For example, a set of five Fe lines has a detection limit of 5.4 ng ml(-1) for the first principal component, compared to the lowest detection limit of 11 ng ml(-1) for Fe II 260.7 09 nm. In addition, the remaining principal components are shown to be independent of analyte concentration, but dependent upon the presence of unknown, additive spectral interferences, The procedure was used t o determine 0.5 mu g ml(-1) of Cr, Mn and V in a matrix containing Ce, La, Dy, Fe, Mo and Co, Six Cr lines, three Mn lines and seven V lines were used for quantitative analysis. Spectral interferences were corr ectly predicted for 2 Cr lines and 3 V lines, whilst the predicted con centrations for the three analytes were 0.51 +/- 0.01, 0.49 +/- 0.01 a nd 0.51 +/- 0.01 mu g ml(-1), respectively.