Matrix sensitivity of solid sampling AAS. Determination of zinc in geological samples

Abstract

Direct solid sampling techniques in AAS have several advantages over wet digestion methods such as small sample size requirements and simple calibration procedures. But some disadvantages also exist such as the sample in homogeneity and the matrix sensitivity of calibration. The calibration is commonly carried out by varying the sample mass and evaluating the peak intensity versus absolute analyte amount. It is shown here that this procedure must be considered doubtful when matrix effects are expected. In the case of zinc determination in geological samples it has been shown that calibration functions obtained by different reference materials differ significantly from each other. As an alternative a three-dimensional calibration technique can be applied that evaluates the peak intensity versus both analyte content and sample weight. The resulting calibration planes are expected to be hyperbolically curved. This three-dimensional calibration has been applied to the determination of Zn in geological samples and compared with classical solid sampling AAS calibration procedures.