Control of interferences in the determination of Pt, Pd and Rh in airborneparticulate matter by inductively coupled plasma mass spectrometry

The development of methods for the determination of Pt, Pd and Ph (platinum group elements (PGEs)) in environmental samples has attracted considerable interest in recent years due to the spread of these elements into the envi ronment mainly from cars fitted with exhaust catalysts. This work studies t he direct determination of PGEs at ultratrace level in contaminated airborn e samples by quadrupole inductively coupled plasma mass spectrometry (Q-ICP -MS) after mathematical correction of interferences. The interference contr ibution of HfO+ in Pt-195 determination, of Pb2+, ArCu+, SrO+ and RbO+ in R h-103 determination and that of YO+, ArCu+ and ArGa+ in Pd-105 determinatio n was studied in order to find the best analyte/interferent signal ratio. T he influence of instrumental parameters such as nebuliser gas flow rate and plasma power was evaluated. The results showed that argon gas flow rate ca nnot be used for interference alleviation and that, in general, a medium pl asma power of 1350 W yields the best ratio, although Pb2+ formation is mini mised at 1150 W. The detection limits obtained were 0.6, 3.3 and 0.9 ng l(- 1) for Pt, Pd and Ph, respectively, and the relative standard deviation (RS D) (50 ng l(-1), n = 5) was <3%. Analysis of airborne samples collected bes ide the Madrid M-30 ring road on cellulose filters with PM 10 impactors and filter mineralisation in a microwave oven using aqua regia/HF solutions sh owed that the PGE content is at the pg m(-3) level. Pt can be determined wi thout major errors, the HfO+ contribution being about 10%. Pd determination is hampered by the conjugate factors of very low Pd concentration in these samples and a matrix with a high content of Cu and Y, whose interference c ontribution is enormous. The contribution of interferences to the Ph conten t in airborne particles is in the range of 50-75%, and after mathematical c orrection, the Ph content can be evaluated. (C)2000 Elsevier Science B.V. A ll rights reserved.