A method for semi-continuous measurement of dissolved elemental mercury in industrial and natural waters.

Mercury in aqueous systems can be present in different chemical forms. Of these, dissolved elemental Hg(0) (DEM) is of great importance because it can readily be partitioned between air and water. Analytical methods used for determining DEM are conventionally based on removal of Hg(0) by purging, pre-concentration on gold and detection by either cold vapour atomic absorption (CV-AAS) or atomic fluorescence spectrophotometry (CV-AFS). At present, there is no agreed protocol for the measurement of DEM in aqueous samples. A new method is described here, which is based on continuous stripping of DEM by mercury-free nitrogen in a flow injection mode and detection by CV-AAS. The partitioning of DEM between aqueous and gas phases is largely dependent on the composition of the former. Moreover, calibration using the standard addition method is not possible due to the reactivity of DEM introduced from calibration solutions. Calibration is therefore done by reference measurements using a manual method for DEM involving quantitative removal and CV-AFS detection. DEM is then determined in the water sample by applying the partitioning factor. The optimised method is precise, sensitive and linear over a wide concentration range. It has provided comparable results with the manual method when applied on board a research vessel in the Mediterranean Sea (0.02–0.05 ng L−1) and during a pilot laboratory-scale experiment on industrial aqueous media from wet flue gas desulphurisation (WFGD) equipment (2–300 ng L−1). [ABSTRACT FROM AUTHOR]