The role and impact of chromium (Cr) on the environment and living organisms depends primarily on its chemical form. High toxicity of hexavalent Cr is well documented, while trivalent Cr is an essential micronutrient. In the last decades numerous analytical procedures have been developed for the determination of Cr(VI) in different sample matrices. To obtain reliable speciation data it is important to preserve species integrity during the sample storage, pre-treatment, extraction and the determination of Cr species. Among different speciation methods combination of high performance liquid chromatography (HPLC) with atomic spectrometry techniques provides comprehensive information on the presence of Cr species in a variety of sample matrices, while hyphenation of HPLC to inductively coupled plasma mass spectrometry (ICP-MS) represents the most powerful and the most sensitive analytical tool for Cr speciation. Precise isotope ratio measurement enables the application of isotope dilution techniques for the quantification of trace amounts of individual Cr species in various environmental and biological samples. Furthermore, enriched stable isotopes can be introduced as tracers to investigations on the fate and role of Cr in the environment and living organisms or to monitor the species transformation during the analytical procedure. Despite general understanding of Cr chemistry, which is closely related to its trivalent and hexavalent oxidation states and knowledge on conditions that may influence species transformation, there are still open questions that should be addressed to obtain reliable speciation analysis data. So, this article is focused mostly to overview recent developments in methodological approaches for Cr speciation in different sample matrices by applying HPLC and spectrometric techniques. Different procedures for preparation of isotopically enriched Cr spike solutions are critically evaluated. The advantages of their use as tracers to follow and account for species transformation during sample preparation and for the quantification of Cr species by HPLC-ID-ICP-MS are discussed. The importance of the use of adequate analytical methodologies and speciation analysis in the determination of Cr(VI) is highlighted in order to avoid inadequate conclusions to be made based on wrongly applied analytical methodologies. An increasing need to develop speciation procedures for selective determination of Cr(III) species is also emphasized.

The extent of pollution was investigated in sediments collected along the course of the river Meža and its tributaries in the lead and zinc mining area of the Mežica valley (Slovenia). In order to evaluate the heavy metal burden, total concentrations of Zn, Pb and Cd were determined and the partitioning of these metals between the easily and sparingly soluble sediment fractions was performed by the use of the slightly modified BCR sequential extraction procedure. The quality of analytical data was checked with Certified Reference Material CRM 601. Good agreement between the determined and certified or indicative metal concentrations was obtained. In order to estimate the natural and anthropogenic inputs of Zn, Pb and Cd in the sediments, normalisation to Al was applied. The results of the partitioning study indicate that Zn prevails in the most sparingly soluble fraction and is distributed between organic matter and sulfides, while a smaller proportion is found in the easily soluble fraction. Pb is distributed mainly between organic matter and sulfides, whereas Cd is predominantly associated with the most sparingly soluble fraction. Data from the normalisation procedure indicate that the anthropogenic inputs of Zn, Pb and Cd correlate with the very high total metal concentrations determined in sediments. The highest total Zn, Pb and Cd concentrations (16.3, 9.3 and 0.13 g kg⁻¹, respectively) were found in the sediment of the Helena rivulet, arising from former mining activities. In spite of the relatively low easily soluble metal fractions in the sediment, the concentrations of metals in these fractions are high, owing to the extremely high total metal concentrations. These data indicate severe pollution of the terrestrial and aquatic environment.

During a sampling campaign in September 2015, elevated chromium (Cr) concentrations were observed in sediments of industrially exposed sites of the Sava River (stainless steel production and impact of metallurgic industry). To verify if sediments also contained hazardous hexavalent Cr (Cr(VI)), there was a need to develop a sensitive and reliable analytical procedure for its determination. In the determination of Cr(VI) in environmental samples, it is necessary to evaluate the suitability of the applied analytical methodology for each individual sample matrix. In these studies, the use of isotopically enriched Cr tracers importantly contribute to the validity of the obtained results. In the present work, an analytical procedure was optimised for the extraction of total Cr(VI) from sediments and the content of Cr(VI) determined by high performance liquid chromatography coupled to inductively coupled plasma mass spectrometry (HPLC-ICP-MS). To leach the total amount of Cr(VI) from sediments, an ultrasound-assisted extraction procedure was applied at 80 °C, using 2% NaOH + 3% Na2CO3 as the extraction solution. The addition of 0.4 mol L-1 MgCl2 prevented oxidation of Cr(III) during the extraction step. To control for species interconversion and for an accurate calculation of Cr(VI) concentration by speciated isotope dilution (ID)-ICP-MS, the alkaline extract was doubly spiked with enriched 50Cr(VI) and 53Cr(III). The accuracy of the determination of Cr(VI) was verified by analysing the certified reference material CRM 041 (Cr(VI) in soil), and by spike recovery test. Low limits of detection (LOD) and quantification (LOQ) (1.25 and 4.0 μg Cr(VI) kg-1, respectively) and good repeatability of measurement (relative standard deviation better than ±4.8%) were obtained. The analytical data revealed that Cr(VI) concentrations in sediments of the Sava River did not represent any known environmental hazard.