543.42To increase the sensitivity of the atomic-absorption analysis, we suggest concentrating the analytes on a tungsten probe through multiple fractional condensation of the sample vapor obtained in a graphite atomizer. This technique makes it possible to additionally reduce the matrix interference. To this end, a sample with a high interference level is preliminarily diluted to the level eliminated by the stage of fractional condensation and then concentrated on the probe. The influence of potassium sulfate on the Pd, Cd, and Ag absorption has been reduced by a factor of 1.5-4.5 and that of sodium chloride -by a factor of 4-300 compared to the influences in the longitudinally heated atomizer with a platform, a modifier, and a background corrector based on the Zeeman effect. In a number of cases, advantages over the transversely heated atomizer have been attained.Introduction. For atomic-absorption determination of elements whose concentration is below the detection limit of the spectrometer, the sample concentration is used. If the content of interfering components in the sample is small, then concentration is carried out directly in the electrothermal atomizer, dosing multiply and drying before the sample atomization step and absorption measurement. Otherwise, to eliminate matrix interferences, one has to take recourse to more laborious and expensive methods of extraction or flowing injection with a concentration of elements in selectively sorbing microcolumns [1]. Earlier [2], we reported on a decrease in matrix interferences in a graphite tubular atomizer by a few orders of magnitude by means of the stage of fractional condensation (FC) of elements on a tungsten probe. At this stage the matrix volatilizes to a considerable extent from the atomizer and reevaporation of elements from the probe occurs without its influence. The probe set at the FC stage over the dosing port of the atomizer traps the analytes from the outgoing flow of sample vapors and lets the matrix components pass. However, beginning with a certain matrix content in the sample, such a selective trap loses its efficiency. This can be due to the formation in the gaseous phase of molecules and condensed particles of the matrix, which, trapping the elements, prevent their deposition on the cold surface of the probe. To get out of such a situation, it is logical to dilute the sample to a level acceptable by the probe and realize several sequential stages of FC, simultaneously concentrating the element and reliably removing the matrix. In the present work, this technique has been used for lead, cadmium, and silver with a high content of chloride and sulfate matrices that are problematic to analyze directly in production-type graphite atomizers, even those using a platform, a modifier, and a Zeeman-effect background corrector, i.e., under the conditions of the universally accepted concept of the stabilized temperature platform furnace (STPF) [3].The experiments were performed on an AAS-30 atomic-absorption spectrometer with a deuterium background co...