scholarly journals Traceable Determination of Atmospheric Mercury Using Iodinated Activated Carbon Traps

Atmosphere ◽  
2020 ◽  
Vol 11 (8) ◽  
pp. 780
Author(s):  
Igor Živković ◽  
Sabina Berisha ◽  
Jože Kotnik ◽  
Marta Jagodic ◽  
Milena Horvat

Traceable determination of atmospheric mercury (Hg) represents a major analytical problem due to low environmental concentrations. Although Hg pre-concentration on activated carbon (AC) traps is a simple method for sample collection, Hg determination is difficult due to a complex matrix that cannot be easily digested using wet chemistry. Two approaches for Hg loading on iodinated AC, the purging of elemental mercury (Hg0) and the spiking a solution of standard reference material (SRM), were used to test whether spiking SRM solution on AC can be used for the traceable determination of atmospheric mercury collected as Hg0. Mercury on AC was determined using atomic absorption spectrometry after sample combustion. The detector’s response for both loading methods was identical in a wide concentration range, indicating that the spiking of SRM on AC can, indeed, be used for the calibration of analytical systems used for the determination of atmospheric mercury. This was confirmed by the determination of Hg in a real atmospheric sample collected on an iodinated AC trap and using an SRM spiking calibration. Different ACs were compared regarding their ability to quantitatively capture Hg while having the lowest breakthrough. Use of a specific impregnating solution probably converted Hg on AC to Millon’s iodide, as estimated from the fractionation thermogram.

2016 ◽  
Vol 16 (5) ◽  
pp. 3061-3076 ◽  
Author(s):  
David S. McLagan ◽  
Maxwell E. E. Mazur ◽  
Carl P. J. Mitchell ◽  
Frank Wania

Abstract. Because gaseous elemental mercury (GEM) is distributed globally through the atmosphere, reliable means of measuring its concentrations in air are important. Passive air samplers (PASs), designed to be cheap, simple to operate, and to work without electricity, could provide an alternative to established active sampling techniques in applications such as (1) long-term monitoring of atmospheric GEM levels in remote regions and in developing countries, (2) atmospheric mercury source identification and characterization through finely resolved spatial mapping, and (3) the recording of personal exposure to GEM. An effective GEM PAS requires a tightly constrained sampling rate, a large and stable uptake capacity, and a sensitive analytical technique. None of the GEM PASs developed to date achieve levels of accuracy and precision sufficient for the reliable determination of background concentrations over extended deployments. This is due to (1) sampling rates that vary due to meteorological factors and manufacturing inconsistencies, and/or (2) an often low, irreproducible and/or unstable uptake capacity of the employed sorbents. While we identify shortcomings of existing GEM PAS, we also reveal potential routes to overcome those difficulties. Activated carbon and nanostructured metal surfaces hold promise as effective sorbents. Sampler designs incorporating diffusive barriers should be able to notably reduce the influence of wind on sampling rates.


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