The stability of Se(IV) and Se(VI) species at 10 and 50 ng ml(-1) conc
entrations, at different pH values, in the presence or absence of chlo
ride and stored at different temperatures and in different containers
was reported. Se(IV) was determined by hydride generation atomic absor
ption spectrometry (HG-AAS) and Se(VI) by reducing Se(VI) to Se(IV) an
d calculating the difference between total inorganic Se and Se(IV). Ne
utron activation analysis (NAA) was used for quality control. Complete
loss of Se(IV) occurred after twelve months when samples were stored
in polyethylene containers at pH 2 in the absence and in the presence
of chloride. Se(VI) was stable under those conditions fos the twelve m
onths tested. The stability of Se(IV) increased at pH 6, with two mont
hs being the maximum storage time without risk of Se(IV) loss. The pre
sence of Cl- decreased the risk of losses in some cases. PTFE containe
rs increased Se(IV) losses at pH 6, especially at 10 ng ml(-1). Both s
pecies were stable at -20 degrees C for the twelve months tested and l
osses of Se(IV) and Se(VI) were lower at 40 degrees C than at room tem
perature. A discussion of these results and data published in the lite
rature are included in this paper.