Mercury speciation in hair by headspace injection–gas chromatography–atomic fluorescence spectrometry (methylmercury) and combustion-atomic absorption spectrometry (total Hg)

The speciation of Hg in human hair was carried out with combustion-atomic absorption spectrometry for total Hg (THg) and headspace–gas chromatography–atomic fluorescence spectrometry (HS–GC–AFS) for methylmercury (MMHg). termination of total Hg in hair was carried out with the AMA analyzer (Advanced Mercury Analyser 254). Accuracy and reproducibility were assessed on a Certified Reference hair sample (IAEA-086 CRM), yielding, respectively, a recovery of 97.5% and a RSD of 3.2%. Analyses of 10 blank measurements resulted in a detection limit of 1.5 ng g−1 of THg for a 20 mg sample of human hair. oncentrations in hair were assessed with HS–GC–AFS in a single analysis step. Either acid or alkaline extraction can be applied because they yielded very similar results on a IAEA-086 CRM: we observed a recovery of 103% and a RSD of 7% with acid extraction and a recovery of 110% and a RSD of 9% with alkaline extraction. Optimization of the headspace vial, injection and GC parameters is described. The detection limit of the MMHg determination in human hair, which amounts to 0.04 ng g−1 for a 20 mg sample, is far below the concentrations observed in natural samples. mber of samples that can be analyzed per hour, respectively, amounts to 8 for THg and 4 for MMHg. Finally, Hg speciation in natural human hair samples was carried out by combining both AMA and HS–GC–AFS analysis methods. THg levels were at the μg g−1, level, with an average MMHg fraction of about 70%.