Homogeneous liquid-liquid extraction followed by X-ray fluorescence spectrometry of a microdroplet on filter-paper for the simultaneous determinationof small amounts of metals

Citation
S. Igarashi et al., Homogeneous liquid-liquid extraction followed by X-ray fluorescence spectrometry of a microdroplet on filter-paper for the simultaneous determinationof small amounts of metals, ANALYST, 125(5), 2000, pp. 797-798
Citations number
12
Categorie Soggetti
Chemistry & Analysis","Spectroscopy /Instrumentation/Analytical Sciences
Journal title
ANALYST
ISSN journal
00032654 → ACNP
Volume
125
Issue
5
Year of publication
2000
Pages
797 - 798
Database
ISI
SICI code
0003-2654(2000)125:5<797:HLEFBX>2.0.ZU;2-A
Abstract
Homogeneous liquid-liquid extraction with perfluorooctanate ion (PFOA(-)) w as utilized for the preconcentration of certain types of metal chelates, su ch as diethyldithiocarbamate, 1,10-phenanthroline and desferrioxamine B. Un der the experimental conditions {i.e., [PFOA(-)](T) = 6.0 x 10(-3) mol l(-1 ), [acetone](T) = 2.0 vol%, [HCl](T)=0.72 mol l(-1), room temperature}, the maximum concentration factor was 500-fold. A method was then developed to determine those metal chelates deposited in a microdroplet on filter-paper using X-ray fluorescence spectrometry. As a result, when three types of che lating agent were used together in the process, 15 metal ions [Ti(IV), Zr(I V), V(V), Nb(V), Ta(V), W(VI), Fe(II), Co(II), Ni(II), Pd(II), Cu(II), Au(I II), Hg(II), Bi(III) and Se(IV)] were simultaneously determined. The recove ry of each metal was ca. 83-100%, except for W(VI) which was 60.2%. The cal ibration curves for each metal ion were linear over the range from 5.0 x 10 (-7) to 1.0 x 10(-5) mol l(-1). The detection limits were at the 10(-8) mol l(-1) level and the relative standard deviations were below 5%.