scholarly journals Rtęć w próbkach mieszanin gazowych – przegląd metod pobierania i oznaczania rtęci

Nafta-Gaz ◽  
2020 ◽  
Vol 76 (11) ◽  
pp. 846-853
Author(s):  
Anna Król ◽  
◽  
Ewa Kukulska-Zając ◽  

The determination of the composition of gas mixtures, especially those analytes which exist, for example, as contaminants for the main components of the gas mixture, very often requires the concentration of the analyte so that it can be quantified. The analysis of gaseous environmental samples, including air and air samples at workplaces, is difficult, which results from: the need to work with samples with an extensive matrix and heterogeneous distribution of pollutants, the stability of the analyte and the presence of interfering substances (interferents) in the sample. On the other hand, the analysis of trace components of gaseous fuels is difficult due to the need to collect a suitably concentrated sample so that these components can be quantified. This article provides an overview and analysis of the methods used for the collection and determination of mercury in gas mixtures. Currently, there are standardized mercury collection and determination methodologies dedicated to matrices such as air, workplace air, waste gases or natural gas. These are both manual and fully automated methods. Most of the methods described in the literature on the subject consist of two stages, i.e. the stage of collecting a sample for a solid or liquid sorbent and the stage of desorption and determination of the mercury content in the collected sample using methods dedicated to the analysis of this element. The most frequently used methods for collecting mercury samples in gas mixtures are: the gold amalgamation method and the sorption methods on powder sorbents (such as activated carbon, hopcalite, impregnated silica gel), glass fibers, impregnated cellulose filters and liquid sorbents (such as e.g. acids). The methods of sample desorption are varied and depend on the material on which the analyte has been absorbed and the selected mercury determination method. Three methods are mainly used to analyze samples for mercury content, i.e. the cold vapor atomic absorption spectrometry method (CV-AAS), the cold vapor fluorescence atomic spectrometry method (CV-AFS) and the inductively coupled plasma mass spectrometry method (ICP-MS). However, it should be kept in mind that although the methods available and used for the analysis of mercury content in gas are standardized, they are not resistant to the presence of hydrocarbons and hydrogen sulphide in the tested samples. These are the compounds that are most often mentioned as substances interfering in the determination of mercury in gases using the above-mentioned methods.

2012 ◽  
Vol 56 (4) ◽  
pp. 585-589 ◽  
Author(s):  
Agnieszka Nawrocka ◽  
Józef Szkoda

Abstract Procedure for determination of chromium in biological materials by Zeeman graphite furnace atomic absorption spectrometry method using a Perkin-Elmer spectrometer equipped with hollow-cathode lamp at 357.9 nm was developed. The samples of animal tissues, food, and feed were digested in muffle furnace at 450ºC. The ash was dissolved in 1 N hydrochloric acid and the final solution was diluted in 0.2% nitric acid. Magnesium nitrate (1%) was used as a matrix modifier. The method was validated in terms of basic analytical parameters. The mean recoveries of chromium was 84.4% for muscle, 79.0% for canned meat, and 80.2% for feed, and analytical detection limit was 0.003 μg/g. Certified reference materials were used for analytical quality assurance. The proposed analytical procedure is well adapted for monitoring chromium content in food and feedstuffs. Content of total chromium in the tested samples (animal muscles and liver) was low and was situated in the range of 0.031-0.101 mg/kg (muscles) and 0.047-0.052 mg/kg (liver).


2020 ◽  
Vol 35 (1) ◽  
pp. 136-144 ◽  
Author(s):  
Flávio V. Nakadi ◽  
Raúl Garde ◽  
Márcia A. M. S. da Veiga ◽  
Julio Cruces ◽  
Martín Resano

Production of dried blood spots and dried urine spots of known volume enables their direct analysis aiming at the fast quantification of Hg.


2011 ◽  
Vol 94 (4) ◽  
pp. 1304-1309 ◽  
Author(s):  
Regina Terumi Yamaki ◽  
Luana Sena Nunes ◽  
Hygor Rodrigues De Oliveira ◽  
André S Araújo ◽  
Marcos Almeida Bezerra ◽  
...  

Abstract The synthesis and characterization of the reagent 2-(5-bromothiazolylazo)-4-chlorophenol and its application in the development of a preconcentration procedure for cobalt determination using flame atomic absorption spectrometry after cloud point extraction is presented. This procedure is based on cobalt complexing and entrapment of the metal chelates into micelles of a surfactant-rich phase of Triton X-114. The preconcentration procedure was optimized by using a response surface methodology through the application of the Box-Behnken matrix. Under optimum conditions, the procedure determined the presence of cobalt with an LOD of 2.8 μg/L and LOQ of 9.3 μg/L. The enrichment factor obtained was 25. The precision was evaluated as the RSD, which was 5.5% for 10 μg/L cobalt and 6.9% for 30 μg/L. The accuracy of the procedure was assessed by comparing the results with those found using inductively coupled plasma-optical emission spectrometry. After validation, the procedure was applied to the determination of cobalt in pharmaceutical preparation samples containing cobalamin (vitamin B12).


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