Nikiel i jego związki. Metoda oznaczania w powietrzu na stanowiskach pracy

Nickel due to its physicochemical properties is used to produce high strength, corrosion resistant, temperature resi-stant, high resistance and acid resistant alloys. Nickel in the form of fine powder can induce an allergic response when in contact with the skin, carcinogenic properties have been proven with long-term exposure to nickel dust. According to the proposed directive of the European Parliament No. 2020/0262, a value of maximum allowable concentration (MAC) in a workplace air in Poland for the inhalable fraction should be at 0.05 mg/m3 and for the respirable fraction at 0.01 mg/m3 (2020/0262/COD). The aim of this study was to develop a method for determining nickel in the range of 1/10 ÷ 2 of the MAC. The method is based on gathering nickel aerosol and its compounds contained in the air on a filter, filter mineralization in nitric acid(V) and hydrochloric acid at elevated temperature then determination of nickel content in the sample using atomic absorption spectrometry (AAS) with flame atomization. The method for the determination of nickel is presented in the form of an analytical procedure, which is included in the appendix. This article discusses the problems of occupational safety and health, which are covered by health sciences and environmental engineering.

Związki manganu, niklu i żelaza. Metoda oznaczania w powietrzu na stanowiskach pracy

The aim of this study was to develop and validate a method for determining of inhalable and respirable fraction of compounds of manganese, nickel and iron in workplace air. The method is based on passing the tested air through a filter from the cellulose ester mixture placed in a specific sampler. The filter mineralizes in concentrated nitric acid (V) and makes a solution for analysis in diluted nitric acid (V). The use of different dilutions of the sample solution after mineralization makes it possible to use the ranges of standard curves for the determination of substances as manganese, nickel and iron. The addition of lanthanum salt (correction buffer) prevents the occurrence of chemical interference, the use of deuterium lamp eliminates background interference. The developed method enables the determination of selected substances in the air of the working environment in the concentration ranges corresponding to the range from 0.1 to 2 MACs values and also enables the determination of nickel and its compounds in the inhalable fraction for the currently proposed new value of the maximum permissible concentration. The developed method has been validated in accordance with the requirements of Standard No. PN-EN 482 and good validation results were obtained. The method can be used for assessing occupational exposure to compounds of manganese, nickel and iron and associated risk to workers’ health. The developed method of determining compounds of manganese, nickel and iron has been recorded as an analytical procedure (see Appendix). This article discusses the problems of occupational safety and health, which are covered by health sciences and environmental engineering.

Organic Ion-Associate Phase Microextraction/Back-Microextraction for Preconcentration: Determination of Nickel in Environmental Water Using 2-Thenoyltrifluoroacetone via GF-AAS

An ion-associate phase (IAP) microextraction/ back-microextraction system was applied for the enrichment, separation, and detection of trace amounts of nickel from environmental water samples. Thenoyltrifluoroacetone (HTTA) acted not only as a chelating reagent for nickel, but also as a component of the extraction phase, i.e., IAP. Nickel in a 40 mL sample solution was pH-adjusted with phenolsulfonate (PS−) and tetramethylammonium hydroxide and converted by chelation reaction in the presence of thenoyltrifluoroacetonate (TTA−). When benzyldodecyldimethylammonium ion (C12BzDMA+) was added, a suspension of IAP formed in the solution. The IAP consisted of TTA−, a chelating reagent, the PS−, a component of pH buffer, and C12BzDMA+, which helps extract the chelating complex. When the solution was centrifuged, the IAP separated from the suspension and the nickel-TTA chelate was extracted into the bottom phase of the centrifuge tube. After the aqueous phase was taken away, 100 µL of nitric acid (2 M) solution containing phosphate was used to back-microextract nickel from the IAP. The acid phase was measured via graphite-furnace atomic-absorption spectrometry (GF-AAS). The proposed method facilitated a 400-fold enrichment. The limit of detection was 0.02 µg L−1. The proposed method was applied for the determination of nickel in river water and seawater samples.

Determination of Nickel and Cadmium in Freshwater Fishes at Sungai Kuantan, Sungai Riau And Sungai Pinang

Heavy metal exhibit toxic and persistent characteristics, can enter into the food chains and the ecosystem where they cause adverse impact on the biotic and abiotic components of ecosystem. Heavy metal pollution in Malaysia has become a major health concern for humans. Thus, this study was conducted to determine the level of cadmium (Cd) and nickel (Ni) in the muscle and gill of fishes collected from the Sungai Kuantan and Sungai Riau. Field sampling was conducted between September and December 2017. Five different species of fishes: Barbonymus gonionotus (Lampam Jawa), B. schwanenfeldii( Lampam Sungai), Hampala macrolepidota(Sebarau), Chitala chitala (Belida), and Hemibagrus nemurus(Baung) were digested by using acid digestion method and analysed with Inductively Coupled Plasma-Mass Spectrometry (ICPMS). Concentration of Cd among species were in order of: H. macrolepidota >B.gonionotus> B. schwanenfeldii> C.chitala> H.nemurus, whereas Ni level in fishes were: C. chitala> H. macrolepidota> B. gonionotus> H. nemurus> B. schwanenfeldii. Among all the species, H. macrolepidota from Sungai Kuantan had the highest Cd in both muscle (0.1761±0.0062¬mg/kg) and gills (0.2938±0.0066mg/kg) whereas the highest Ni level in muscle was noted in C. chitala from Sungai Kuantan with (0.1473±0.0755 mg/kg) and in gills of B.gonionotus (0.4544±0.0470mg/kg) from the same river respectively. It was obtained that there was a significant difference (p<0.05) of Cd in muscle between species. Ni concentration in fishes was below the permissible limit stipulated by World Health Organizations WHO (1985) and Food and Agriculture Organizations (2012) but the concentration of Cd was recorded high. However, it was still below the World Health Organization (WHO) 1985 and Malaysian Food Act (MFA) 1983.

Sorption-spectrometric determination of nickel by monoammonium salt of glycirrizic acid

There was obtained IR spectra of the nickel diglycyrrhizinate complex. A simple and express spectral method for determination of the nickel ion is presented. The optimal conditions for the determination of the nickel ion are found. Under optimal conditions, a gradual graph was drawn up, which is linear in the concentration range for nickel of 20.0–40.0 μg/25 ml, the composition of the complex of nickel with the monoammonium salt of glycyrrhizic acid (MASGA) were determined.