RESUMO
An effective analytical method for bromine and iodine determination in human hair using interference-free inductively coupled plasma mass spectrometry (ICP-MS) was developed. Human hair was digested based on combustion reaction to obtain compatible solutions with ICP-MS analysis. Using microwave-induced combustion (MIC), masses of human hair ranging from 50 to 300â¯mg were efficiently digested. Only a diluted alkaline solution (100â¯mmolâ¯L-1â¯NH4OH) was used for the absorption of both analytes, which was fully compatible with ICP-MS analysis. Using these conditions low limits of detection were obtained (LOD of 0.01⯵gâ¯g-1 for Br and 0.004⯵gâ¯g-1 for I). Recovery tests at two levels (50% and 100%) using a standard solution or mixtures of the sample with certified reference materials (CRMs) were carried out to evaluate the suitability of proposed method and recoveries between 94% and 102% were always obtained. Accuracy was evaluated by analysis of a human hair CRM, and the Br and I concentrations obtained by the proposed method did not differ significantly from those described in the certificate. Repeatability (RSDsâ¯≤â¯4%) and reproducibility (RSDsâ¯≤â¯7%) of the results using proposed method were always very suitable. The digests obtained using the MIC method were fully compatible with ICP-MS and the interferences currently found using conventional digestion methods were completely eliminated. Ultra-trace concentrations of Br and I were determined in human hair, demonstrating that the proposed method is a suitable strategy, and it presents several advantages compared to others published in the literature.
Assuntos
Bromo/análise , Cabelo/química , Iodo/análise , Humanos , Espectrometria de Massas , Micro-OndasRESUMO
A simple and automated system based on combustion followed by a pyrohydrolysis reaction was proposed for further halogens determination. This system was applied for digestion of soils containing high (90%) and also low (10%) organic matter content for further halogens determination. The following parameters were evaluated: sample mass, use of microcrystalline cellulose and heating time. For analytes absorption, a diluted alkaline solution (6â¯mL of 25â¯mmolâ¯L-1â¯NH4OH) was used in all experiments. Up to 400â¯mg of soil with high organic matter content and 100â¯mg of soil with low organic matter content (mixed with 400â¯mg of cellulose) could be completely digested using the proposed system. Quantitative results for all halogens were obtained using less than 12â¯min of sample preparation step (about 1.8â¯min for sample combustion and 10â¯min for pyrohydrolysis). The accuracy was evaluated using a certified reference material of coal and spiked samples. No statistical difference was observed between the certified values and results obtained by the proposed method. Additionally, the recoveries obtained using spiked samples were in the range of 98-103% with relative standard deviation values lower than 5%. The limits of quantification obtained for F, Cl, Br and I for soil with high (400â¯mg of soil) and low (100â¯mg of soil) organic matter were in the range of 0.01-2⯵gâ¯g-1 and 0.07-59⯵gâ¯g-1, respectively. The proposed system was considered as a simple and suitable alternative for soils digestion for further halogens determination by ion chromatography and inductively coupled plasma mass spectrometry techniques.