IntroductionThe determination of non-metals via molecular hyperfine structured rotational lines of diatomic molecules generated between the analyte and a molecule forming element has been successfully performed using high-resolution continuum source atomic absorption spectrophotometers (HR-CS-AAS). For this purpose, Ga, 1-3 Ca, 4 Al, 5 Sr 6 etc. were used to form the diatomic molecules of halogens, whereas CS rotational lines formed in the presence of excessive carbon in flames and a graphite furnace were benefited for the determination of S. 7,8 Various mechanisms can be proposed for the formation of diatomic molecule of halogens in a graphite furnace: (i) a salt of analyte is formed upon interaction with the molecule-forming elements during the drying step, which is later decomposed at elevated temperature to produce a diatomic molecule and/or (ii) the atoms of the analyte and the molecule forming element are combined in the gas phase to form the diatomic molecule. This gas-phase interference occurred during metal and metalloid determination by the atomic absorption, and every attempt was made to reduce it to obtain free gaseous analyte atoms, although it is helpful to form the diatomic molecule during the determination of halogens. Of course, another mechanism may be responsible from diatomic molecules of the analyte, but whatever it is, the diatomic molecule is formed upon interaction of the halogen with the molecule-forming element either in the condensed phase (solid and/or liquid phase depending on the temperature) and/or in the gas phase.For investigating the interference mechanisms during the determination of metals by graphite furnace atomic absorption spectrometry (GFAAS), the analyte and interferent were pipetted on different locations in the graphite furnace 9,10 or cavities of a specially designed dual cavity platform. [11][12][13][14][15][16][17][18] The results were compared with those of mixed injections. It was assumed that if the analyte and the interferent were separated, they subsequently do not contact in the condensed phase. Therefore, any interference should be due to the gas-phase interactions between the analyte and the interferent. If they mixed, both condensed-phase and gas-phase interferences are expected. Comparing the results, i.e. the change of the sensitivities for the two cases, made it possible to distinguish the condensed-phase and the gas-phase interferences.In this study, the formation mechanisms of SrF, which was selected as a diatomic molecule for the determination of F, was investigated. For this purpose, the analyte and the moleculeforming element were mixed as well as separately injected on the platform of the graphite furnace. Then, the sensitivities, peak shapes and appearance times for the two cases were compared in order to interpret the SrF formation mechanisms. In previous work, Sr was proved to be a useful moleculeforming element for the determination of F. 6 Therefore, to interpret molecule formation, it is used as a test metal for the formation of a diatomic mo...