Thiourea catalysis of MeHg ligand exchange between natural dissolved organic matter and a thiol-functionalized resin: a novel method of matrix removal and MeHg preconcentration for ultratrace Hg speciation analysis in freshwaters

• Published in: Analytical and bioanalytical chemistry Vol. 388; no. 2; pp. 341 - 352
• Main Authors: Vermillion, Brian R, Hudson, Robert J. M
• Format: Journal Article
• Language: English
• Published: Germany Berlin/Heidelberg : Springer-Verlag 01.05.2007; Springer Nature B.V
• Subjects: Acidification; Adsorption; Algorithms; Catalysis; Chromatography, Liquid - methods; Dissolved organic matter; Exchanging; Fluorescence; Fluvial sediments; Fresh water; Fresh Water - analysis; Hydrogen-Ion Concentration; Kinetics; Ligands; Matrix algebra; Mercury Compounds - chemistry; methylmercury compounds; Methylmercury Compounds - analysis; Methylmercury Compounds - chemistry; Natural waters; Nitrates - chemistry; Porewater; Reproducibility of Results; Resins; Resins, Synthetic - chemistry; Sediments; solid phase extraction; Solid Phase Extraction - methods; Solid phases; Speciation; Speciation analysis; Spectrometry; Spectrometry, Fluorescence; Styrenes - chemistry; Sulfhydryl Compounds - chemistry; Thiourea; Thiourea - chemistry; Thioureas; Water Pollution, Chemical - analysis; Water sampling
• ISSN: 1618-2642; 1618-2650
• DOI: 10.1007/s00216-007-1207-1

Ultratrace analysis of dissolved MeHg in freshwaters requires both dissociation of MeHg from strong ligands in the sample matrix and preconcentration for detection. Existing solid phase extraction methods generally do not efficiently adsorb MeHg from samples containing high concentrations of natural dissolved organic matter. We demonstrate here that the addition of 10-60 mM thiourea (TU) quantitatively releases MeHg from the dissolved matrix of freshwater samples by forming a more labile complex (MeHgTU⁺) that quantitatively exchanges MeHg with thiol-functionalized resins at pH~3.5 during column loading. The contents of these columns were efficiently eluted with acidified TU and MeHg was analyzed by Hg-TU complex ion chromatography with cold-vapor atomic fluorescence spectrometry detection. Routinely more than 90% of MeHg was recovered with good precision (average relative standard deviation of 6%) from natural waters--obtained from pools and saturated sediments of wetlands and from rivers--containing up to 68.7 mg C L-¹ dissolved organic matter. With the preconcentration step, the method detection limit of 0.29 pg absolute or 0.007 ng L-¹ in 40-mL samples is equivalent to that of the current state-of-the- art as practiced by skilled analysts. MeHg in 20-50-mL samples was completely trapped. On the basis of our knowledge of the chemistry of the process, breakthrough volume should depend on the concentrations of TU and H⁺. At a TU concentration of 12 mM breakthrough occurred between 50 and 100 mL, but overall adsorption efficiency was still 85% at 100 mL. Formation of artifactual MeHg is minimal; only about 0.7% of ambient MeHg is artifactual as estimated from samples spiked with 4 μg L-¹ HgII.