New Methods for Atomic-Absorption Determination of Metals in Aviation and Automotive Gasolines

Author(s):  
G. M. Balak ◽  
S. N. Volgin ◽  
A. N. Privalenko
Author(s):  
G. M. Balak ◽  
◽  
S. N. Volgin ◽  
A. N. Privalenko ◽  
◽  
...  

New methods for direct atomic absorption determination of lead and lithium as antiknock additives components in aviation and automotive gasoline in the concentration ranges 100–1700 (Pb) and 2.5/0.25–100 (Li) mg/L have been developed. To overcome the difference in analytical signals for samples and standard solutions due to concentration values and matrix effects the proper sample dilution and the addition of the blank as pure reagent hydrocarbons mixture in the solutions have been offered. The methods have high precision, are simple and may be recommended for gasoline quality control and identification procedures.


2019 ◽  
Vol 85 (2) ◽  
pp. 12-16
Author(s):  
I. V. Saunina ◽  
E. N. Gribanov ◽  
E. R. Oskotskaya

The sorption of Hg (II), Cd (II), and As (III) by natural aluminosilicate is studied. It is shown that the mineral absorbs those toxicants in a rather wide pH range, quantitative extraction of analytes being achieved in a neutral or close to neutral medium (pH values range within 7.0 - 8.0; 6.3 - 7.5; 7.4 - 8.5 for Hg (II), As (III), and Cd (II), respectively). The effect of the time of phase contact on the degree of extraction of elements is shown. The sorption capacity of the mineral in optimal conditions of the medium acidity (0.06 mmol/g for mercury, 0.31 mmol/g for cadmium, and 0.52 mmol/g for arsenic) is determined. The distribution coefficients attain values of aboutnX 103-nX 104. A new combined method for determination of Hg (II), Cd (II), and As (III) in natural and waste water is developed and tested. The method consists in a preliminary group sorption concentration of the analytes by aluminosilicate, desorption of the analytes from the surface of the mineral and their subsequent atomic absorption determination. The correctness of the method is verified in analysis of spiked samples. The method is easy to use and exhibits high sensitivity, reproducibility and accuracy of analyte determination. The relative standard deviation does not exceed 0.13. Economic availability and possibility of using domestic sorption materials are the important advantages of the proposed procedure which can be used in the practice of laboratories monitoring the quality and safety of environmental objects.


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