<p>Atmospheric mercury speciation is of paramount importance for understanding the behavior of mercury once it is emitted into the atmosphere as gaseous elemental (GEM), gaseous oxidized (GOM) and particulate-bound (PBM) mercury. GOM and PBM sampling are the most problematic steps in the analytical procedure. GOM sampling with speciation traps composed of KCl sorbent materials and KCl trapping solutions are commonly used sampling methods, although the work done at ambient air concentrations is limited. The results of the specificity test showed that the KCl sorbent traps are very specific when using new traps, while their specificity drops dramatically when they are reused. The results of the stability test showed that the highest Hg<sup>2+</sup> losses (up to 5.5 % of Hg<sup>2+</sup> loss) occur when low amounts of Hg<sup>2+</sup> (< 1 ng) are loaded, due to a reduction of Hg<sup>2+</sup> to Hg<sup>0</sup>. GOM losses should be taken into account when using KCl sorbent traps for atmospheric Hg speciation, especially at low ambient GOM concentrations. KCl trapping solutions have also been considered as a selective trapping media for GOM in atmospheric samples. A dimensionless Henry’s law constant was experimentally derived and was used to calculate the solubility of elemental Hg in KCl solution. The degree of GEM oxidation was established by purging elemental Hg calibration gas into a KCl solution and determining the GOM trapped using aqueous phase propylation liquid-liquid extraction GC-AFS. A positive GOM bias was observed due to the solubility and oxidation of GEM in KCl trapping solutions strongly suggesting that this approach is unsuitable for atmospheric mercury speciation measurements.</p>