Simultaneous polarographic determination of isoniazid and rifampicin by differential pulse polarography method and support vector regression

2010 ◽  
Vol 55 (22) ◽  
pp. 6570-6576 ◽  
Author(s):  
Karim Asadpour-Zeynali ◽  
Payam Soheili-Azad
Keyword(s):  
Support Vector Regression ◽  
Differential Pulse ◽  
Polarographic Determination ◽  
Support Vector ◽  
Differential Pulse Polarography ◽  
Pulse Polarography

scholarly journals DIFFERENTIAL PULSE POLAROGRAPHIC DETERMINATION OF ARSENIC IN BITUMINOUS COAL

1998 ◽  
Vol 6 (7) ◽  
pp. 27-32
Author(s):  
M. Nogami Eurica ◽  
M. Dalmeida Gracinda ◽  
Jorge Nozaki
Keyword(s):  
Coal Sample ◽  
Bituminous Coal ◽  
Supporting Electrolyte ◽  
Arsenic Concentration ◽  
Differential Pulse ◽  
Polarographic Determination ◽  
Differential Pulse Polarography ◽  
Acidic Media ◽  
Pulse Polarography

Differential pulse polarography was employed for the determination of arsenic in bituminous coal from Figueiras, Parana, Brazil. The dried coal sample was crushed to -100 mesh, ashed, and treated with reducing reagents in acidic media. The arsine generated was collected and selectively oxidized to Al +3 using an absorbing solution of 0.1 mol.L -1 [tris(hydroxymethyl) aminomethane] ( TRIS) and 0. 002 mol.L -1 silver nitrate. A solution of TRIS and hydrochloric acid, pH -1, was used as supporting electrolyte for differential pulse polarographic determination of Al+3 in the concentration range 0.05 -0.60 μglmL. The average arsenic concentration found was 69.0 ± 2.6 mg.kg -1 and was in agreement with the spectrophotometric method using silver-diethyldithiocarbamate-pyridine.

Analysis of mixtures of 4-nitrotoluene-2-sulphonic acid and 4,4'-dinitrostilbene-2,2'-disulphonic acid by tast polarography, differential pulse polarography and thin layer chromatography

1985 ◽  
Vol 50 (8) ◽  
pp. 1673-1684
Author(s):  
Jiří Barek ◽  
Ivo Daňhel
Keyword(s):  
Thin Layer ◽  
Differential Pulse ◽  
Sulphonic Acid ◽  
Polarographic Determination ◽  
Differential Pulse Polarography ◽  
Pulse Polarography ◽  
Tetramethylammonium Bromide ◽  
Disulphonic Acid ◽  
Layer Chromatography

Conditions are sought for the determination of 4-nitrotoluene-2-sulphonic acid (I) and 4,4'-dinitrostilbene-2,2'-disulphonic acid (II) by TAST polarography within the concentration range of 10-2 - 10-6 mol l-1 and by differential pulse polarography (DPP) within the concentration range of 10-3 - 10-8 mol l-1. DPP is applied to the determination of these substances after the thin layer chromatographic separation of their mixtures. Methods are also worked out for their analysis without prior separation, based either on the combined DPP determination of I and the TAST polarographic determination of the sum of I and II in sulphuric acid solutions, or on the DPP determination of the C=C bond in II and the TAST polarographic determination of the sum of the two substances in tetramethylammonium bromide solutions.

Polarographic Determination of 7-Diethylamino-4-methylcoumarin

1995 ◽  
Vol 60 (5) ◽  
pp. 802-812
Author(s):  
Jiří Barek ◽  
Roman Hrnčíř ◽  
Josino C. Moreira
Keyword(s):  
Mercury Electrode ◽  
Differential Pulse ◽  
Polarographic Determination ◽  
Differential Pulse Polarography ◽  
Whitening Agent ◽  
Polarographic Behaviour ◽  
Pulse Polarography ◽  
Dropping Mercury Electrode ◽  
Technical Products

The polarographic behaviour of the title optical whitening agent was studied in aqueous-methanolic solutions. Conditions for its quantitation were found within the concentration regions of 10 to 100 μmol l-1 by tast polarography, 1 to 100 μmol l-1 by differential pulse polarography on the conventional dropping mercury electrode, and 0.1 to 10 μmol l-1 by differential pulse polarography on a static mercury drop electrode. The analytical procedures developed were applied to the determination of the compound in technical products.

The Polarographic Determination of 1-[4'-(Phenylazo)phenyl]-3,3-dimethyltriazene

1992 ◽  
Vol 57 (11) ◽  
pp. 2248-2262 ◽  
Author(s):  
Jiří Barek ◽  
Dana Dřevínková ◽  
Jiří Zima ◽  
Arnold Fogg
Keyword(s):  
Differential Pulse ◽  
Polarographic Determination ◽  
Differential Pulse Polarography ◽  
Polarographic Reduction ◽  
Optimal Conditions ◽  
Polarographic Behaviour ◽  
Pulse Polarography ◽  
Methanol Medium ◽  
Mixed Water

A study has been made of the polarographic behaviour of genotoxic 1-[4'-(phenylazo)phenyl]-3,3-dimethyltriazene in mixed water-methanol medium. A mechanism has been proposed for its polarographic reduction and optimal conditions have been found for its determination by tast polarography in the concentration range 1 . 10-4 - 2 . 10-6 mol l-1 and using differential pulse polarography in the concentration range 1 . 10-4 - 2 . 10-7 mol l-1.

Polarographic determination of some nitro group-containing pesticides

1983 ◽  
Vol 48 (9) ◽  
pp. 2636-2643 ◽  
Author(s):  
Hana Beňadiková ◽  
Milan Popl ◽  
Věra Jakubíčková
Keyword(s):  
Nitro Group ◽  
Supporting Electrolyte ◽  
Differential Pulse ◽  
Environmental Water ◽  
Polarographic Determination ◽  
Differential Pulse Polarography ◽  
Pulse Polarography ◽  
Water Purity

The differential pulse polarography technique was applied to the determination of some pesticides containing nitro groups in their molecules. The nitro groups were found to be reduced to hydroxylamines or to the corresponding amines. The effect of medium, particularly of pH of the supporting electrolyte, was examined. The pesticides were determined in concentrations less than 10 μg l-1, which shows primose for the application of the technique to environmental water purity monitoring.

Determination of platinum in biological material by differential pulse polarography: Analysis in urine, plasma and tissue following sample combustion

1983 ◽  
Vol 48 (10) ◽  
pp. 2903-2908 ◽  
Author(s):  
Viktor Vrabec ◽  
Oldřich Vrána ◽  
Vladimír Kleinwächter
Keyword(s):  
Biological Material ◽  
Biological Fluid ◽  
Mercury Electrode ◽  
Differential Pulse ◽  
Differential Pulse Polarography ◽  
Linear Calibration ◽  
Catalytic Current ◽  
Pulse Polarography ◽  
Dropping Mercury Electrode

A method is described for determining total platinum content in urine, blood plasma and tissues of patients or experimental animals receiving cis-dichlorodiamineplatinum(II). The method is based on drying and combustion of the biological material in a muffle furnace. The product of the combustion is dissolved successively in aqua regia, hydrochloric acid and ethylenediamine. The resulting platinum-ethylenediamine complex yields a catalytic current at a dropping mercury electrode allowing to determine platinum by differential pulse polarography. Platinum levels of c. 50-1 000 ng per ml of the biological fluid or per 0.5 g of a tissue can readily be analyzed with a linear calibration.

Polarography of N,N-dimethyl-4-amino-4'-hydroxyazobenzene in water-methanol mixtures

1985 ◽  
Vol 50 (3) ◽  
pp. 712-725 ◽  
Author(s):  
Jiří Barek ◽  
Lubomír Kelnar
Keyword(s):  
Differential Pulse ◽  
Differential Pulse Polarography ◽  
Polarographic Reduction ◽  
Reduction Mechanism ◽  
Pulse Polarography ◽  
Methanol Medium

The polarographic reduction of N,N-dimethyl-4-amino-4'-hydroxyazobenzene in water-methanol medium was investigated. Evidence is presented for adsorption of the depolarizer on the electrode, and a reduction mechanism is proposed. Conditions are indicated for the determination of this compound in the concentration range 10-4-10-6 mol/l by d.c. polarography, 10-5 to 3 . 10-7 mol/l by Tast polarography, and 10-5-3 . 10-8 mol/l by differential pulse polarography.

Polarographic and voltammetric determination of 6-mercaptopurine and 6-thioguanine

1986 ◽  
Vol 51 (11) ◽  
pp. 2466-2472 ◽  
Author(s):  
Jiří Barek ◽  
Antonín Berka ◽  
Ludmila Dempírová ◽  
Jiří Zima
Keyword(s):  
Detection Limit ◽  
Differential Pulse Voltammetry ◽  
Detection Limits ◽  
Differential Pulse ◽  
Voltammetric Determination ◽  
Differential Pulse Polarography ◽  
Hanging Mercury Drop Electrode ◽  
Pulse Polarography ◽  
Pulse Voltammetry

Conditions were found for the determination of 6-mercaptopurine (I) and 6-thioguanine (II) by TAST polarography, differential pulse polarography and fast-scan differential pulse voltammetry at a hanging mercury drop electrode. The detection limits were 10-6, 8 . 10-8, and 6 . 10-8 mol l-1, respectively. A further lowering of the detection limit to 2 . 10-8 mol l-1 was attained by preliminary accumulation of the determined substances at the surface of a hanging mercury drop.

The polarographic and voltammetric determination of 2,6-dicyano-4-nitro-2'-acetylamino-4'-diethylaminoazobenzene

1990 ◽  
Vol 55 (6) ◽  
pp. 1508-1517 ◽  
Author(s):  
Jiří Barek ◽  
Dagmar Civišová ◽  
Ashutosh Ghosh ◽  
Jiří Zima
Keyword(s):  
Azo Dye ◽  
Differential Pulse ◽  
Differential Pulse Polarography ◽  
Determination Limit ◽  
Polarographic Reduction ◽  
Hanging Mercury Drop Electrode ◽  
Optimal Conditions ◽  
Pulse Polarography ◽  
Pulse Voltammetry

The polarographic reduction of the title azo dye was studied and optimal conditions were found for its analytical utilization in the concentration range 1 . 10-6 - 1 . 10-7 mol l-1 using differential pulse polarography and 1 . 10-6 - 1 . 10-8 mol l-1 using fast scan differential pulse voltammetry or linear scan voltammetry at a hanging mercury drop electrode. When the latter technique is combined with adsorptive accumulation of the studied substance on the surface of the hanging mercury drop, the determination limit can be further decreased to 3 . 10-9 mol l-1.

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