Photometric determination of 2-oxoglutaric acid and some other 2-oxo acids by reaction with 3-methyl-2-benzothiazolinone hydrazone

1984 ◽  
Vol 49 (8) ◽  
pp. 1869-1880 ◽  
Author(s):  
Jiří Šafanda ◽  
Pavel Sobotka

2-Oxoglutaric acid reacts with 3-methyl-2-benzothiazoline hydrazone in acid solutions in the presence of FeCl3 to give a stady yellow colour. The method enables the substance to be determined in concentrations as low as 15 μmol l-1 with an accuracy of about 10%. The analysis can be performed in the presence of some additional natural or synthetic 2-oxo acids. The applicability of the method was tested in the determination of the activity of some enzymes involved in the metabolism of 2-oxoglutaric acid. Glutamic acid can be determined after its prior nonenzymatic transamination. A number of 2-oxo acids including 2-oxoglutaric acid can be determined photometrically with a high sensitivity by reaction with 3-methyl-2-benzothiazolinone hydrazone in conditions favouring the formation of blue tetra-aza-pentamethinecyanine dyes. The molar absorptivities largely lay within the region of (2-4.5) . 104 l mol-1cm-1.

2020 ◽  
Vol 6 (6(75)) ◽  
pp. 54-57
Author(s):  
T.F. Rudometkina

A method for determining the total phosphorus content in foods containing food additives of pyrophosphates and polyphosphates (E 450, E339, E452) is proposed. The reaction of formation of a reduced form of phosphormolybdenum heteropolyacid was used. As a reducing agent, a solution of hydrazine sulfate was used as a reagent that provides high sensitivity of determination . The objects of analysis were: chicken meat Roll "Snezana", processed Cheese "Cheeseburger", Instant coffee "Nescafe Gold Crema," containing food additives of pyrophosphates and polyphosphates (E 450,E339, E452). The correctness of the obtained results was confirmed by the method of additives.


1984 ◽  
Vol 49 (9) ◽  
pp. 2078-2095
Author(s):  
Milan Kotouček ◽  
Josef Růžička

The reactions of gallocyanine methyl ester with germanium(IV) and tin(IV) in 7.7% (m/m) ethanol and with lead(II) in 15.5% ethanol are studied spectrophotometrically. In slightly acid solutions, complexes of GeL3 (pH 2.5-6.5), SnL2 and SnL3 (pH 1.7-6 in the presence oftartaric acid), and PbL and PbL2 (pH 4-7) are formed. The conditional stability constants of the complexes and the equilibrium constants of the complexation reactions are calculated and procedures are suggested for the photometric determination of tin and for the chelometric determination of lead using visual or photometric indication with gallocyanine methyl ester as metallochromic indicator (colour change from red-violet to blue). A gallocyanine methyl ester-methyl orange screened indicator proved useful for the visual determination of lead, showing an expressive colour change from brown to green.


2014 ◽  
Vol 6 (24) ◽  
pp. 9667-9674 ◽  
Author(s):  
Tuanne R. Dias ◽  
Jarbas J. R. Rohwedder ◽  
Marcos A. S. Brasil ◽  
Boaventura F. Reis

This article focuses on the development of an analytical procedure for the photometric determination of vanadium in fresh and mineral waters, implemented employing a downsized multicommuted flow analysis approach.


1985 ◽  
Vol 50 (3) ◽  
pp. 611-620 ◽  
Author(s):  
Jiří Šimek ◽  
Nguyen Truong Son ◽  
Eduard Ružička

The coordination properties of alizarin green series dyes with uranyl ions were studied in the presence of cationoid surfactants (cetylpyridinium bromide, carbethoxypentadecyltrimethylammonium bromide). Ternary complexes of the composition UO2L2S2, UO2L2S4, UO2L2S6, and UO2L3S9, where L is dye and S is surfactant, are formed in weakly acid solutions. The formation constants of the complexes were established and a procedure was worked out for the direct photometric determination of uranium.


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.


2019 ◽  
Vol 85 (10) ◽  
pp. 23-28
Author(s):  
F. S. Aliyeva ◽  
F. O. Mamedova ◽  
F. N. Bahmanova ◽  
Yu. A. Yusibov ◽  
F. M. Chyragov

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