scholarly journals Lead Complexation by Humic Acids and Their Analogs: A Voltammetric Study

Environments ◽  
2020 ◽  
Vol 7 (11) ◽  
pp. 94
Author(s):  
Spencer Steinberg ◽  
Vernon Hodge
Keyword(s):  
Humic Acid ◽  
Humic Acids ◽  
Reduction Potential ◽  
Differential Pulse ◽  
Ligand Concentration ◽  
Differential Pulse Polarography ◽  
Reduction Peak ◽  
Solution Ph ◽  
Voltammetric Study ◽  
Pulse Polarography

Differential pulse polarography (DPP) was used to assess the interaction of Pb2+ with various humic acid analogs and several humic acids. DPP analysis demonstrated that the reduction peak maximum (Ep) for Pb2+ shifted to more negative values in the presence of humic acids and humic acid analogs. The observed Ep for Pb2+ in the presence of humic acids and humic acid analogs is influenced by ligand concentration, solution pH and Pb2+ concentration. Shifts in the Ep for Pb2+ are related to the reduction potential and can be rationalized using the Lingane equation.

scholarly journals Voltammetric Behavior of Zaleplon and Its Differential Pulse Polarographic Determination in Capsules

2005 ◽  
Vol 88 (4) ◽  
pp. 1135-1141 ◽  
Author(s):  
Gipsy Larenas ◽  
Soledad Bollo ◽  
Marcelo Rodriguez ◽  
Igor Lemus ◽  
Luis J Nuñez-Vergara ◽  
...  
Keyword(s):  
Column Liquid Chromatography ◽  
Differential Pulse ◽  
Differential Pulse Polarography ◽  
Content Uniformity ◽  
Reduction Peak ◽  
Buffer Solution ◽  
Pulse Polarography ◽  
Voltammetric Behavior ◽  
Ph Range ◽  
The Individual

Abstract In this work both the electrochemical behavior and the analysis of the hypnotic pyrazolopyrimidine derivative zaleplon were studied. Zaleplon in ethanol–0.1M Britton Robinson buffer solution (30–70) showed 2 irreversible, well-defined cathodic responses in the pH range of 2–12 using differential pulse polarography (DPP), tast polarography, and cyclic voltammetry. From chronocoulometric studies, it was possible to conclude that one electron was transferred in each reduction peak or wave. For analytical purposes, the DPP technique working at pH 4.5 for peak I was selected, which exhibited adequate repeatability, reproducibility, and selectivity. The recovery was 99.97 ± 1.52%, and the detection and quantitation limits were 5.13 × 10−7M and 1.11 × 10−6M, respectively. The DPP method was applied successfully to the individual assay of capsules in order to verify the content uniformity of zaleplon. Treatment of the sample is not required because the excipients do not interfere, the method is not time consuming, and it is less expensive than column liquid chromatography.

A new and sensitive method for the determination of trace arsenic using differential pulse polarography

2014 ◽  
Vol 92 (3) ◽  
pp. 221-227 ◽  
Author(s):  
Güler Somer ◽  
Şükrü Kalaycı
Keyword(s):  
Intermetallic Compound ◽  
Limit Of Detection ◽  
Arsenic Concentration ◽  
Differential Pulse ◽  
Differential Pulse Polarography ◽  
Reduction Peak ◽  
Trace Determination ◽  
Established Method ◽  
Pulse Polarography

A new and simple differential pulse polarographic method has been developed for the trace determination of arsenic. When selenite was added into solutions of some ions such as copper, lead, cadmium, zinc, and chromium, their differential pulse polarographic peak decreased. A new reduction peak appeared at a more positive potential than the ion present and it was always higher than the corresponding reduction peak of the ion. Thus, we made use of this interference for the trace determination of As(III). By the addition of selenite onto As(III), a new As−Se intermetallic compound peak was formed at about −0.35 V (pH at about 1.0–2.0). The trace arsenic concentration could be determined simply from this peak by the addition of standard arsenic into a polarographic cell. In the presence of large amounts of selenite, 2 × 10−7 mol/L As(III) could be determined from this peak precisely. With the newly established method, the limit of detection was 1 × 10−8 mol/L (S/N = 3). Among the most common cations and anions, only Cd−Se and Pb−Se intermetallic compound peaks had an overlap with the As−Se peak. This interference could be eliminated simply by the addition of EDTA. This method was applied successfully for the determination of arsenic in a digested beer sample.

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.

Polarographic and voltammetric determination of N,N’-dinitrosopiperazine

1991 ◽  
Vol 56 (7) ◽  
pp. 1434-1445 ◽  
Author(s):  
Jiří Barek ◽  
Ivana Švagrová ◽  
Jiří Zima
Keyword(s):  
Mercury Electrode ◽  
Linear Sweep Voltammetry ◽  
Differential Pulse ◽  
Differential Pulse Polarography ◽  
Polarographic Reduction ◽  
Concentration Region ◽  
Pulse Polarography ◽  
Chemical Efficiency ◽  
Dropping Mercury Electrode

Polarographic reduction of the genotoxic N,N’-dinitrosopiperazine was studied and its mechanism was suggested. Optimum conditions were established for the determination of this substance by tast polarography over the concentration region of 1 . 10-3 to 1 . 10-6 mol l-1 and by differential pulse polarography on the conventional dropping mercury electrode or by fast scan differential pulse voltammetry and linear sweep voltammetry on a hanging mercury drop electrode over the concentration region of 1 . 10-3 to 1 . 10-7 mol l-1. Attempts at increasing further the sensitivity via adsorptive accumulation of the analyte on the surface of the hanging mercury drop failed. The methods are applicable to the testing of the chemical efficiency of destruction of the title chemical carcinogen based on its oxidation with potassium permanganate in acid solution.

Determination of Organic Bases by Ion-Pair Extraction Polarography Using Orange II as Counter Ion

1992 ◽  
Vol 57 (11) ◽  
pp. 2272-2278 ◽  
Author(s):  
Václav Koula ◽  
Daria Kučová ◽  
Jiří Gasparič
Keyword(s):  
Model Compound ◽  
Differential Pulse ◽  
Ion Pair ◽  
Differential Pulse Polarography ◽  
Orange Ii ◽  
Organic Bases ◽  
Counter Ion ◽  
Pulse Polarography ◽  
Ammonium Compounds

The combination of ion-pair extraction and differential pulse polarography is shown to be a method suitable for the determination of 10-7 mol l-1 concentrations of organic bases of quaternary ammonium compounds. Orange II (4-[2-hydroxy-1-naphtyl]azobenzenesulfonic acid) was found to be an appropriate polarographically active counter-ion. The proposed method was used for the determination of tetrapentylammonium bromide (as model compound), Septonex ([1-(ethoxycarbonyl)-pentadecyl]trimethylammonium bromide) and codeine.

Polarographic Determination of 6-β-D-Glucopyranosyloxy-7-hydroxycoumarin

1996 ◽  
Vol 61 (3) ◽  
pp. 333-341
Author(s):  
Jiří Barek ◽  
Roman Hrnčíř ◽  
Josino C. Moreira ◽  
Jiří Zima
Keyword(s):  
Natural Compound ◽  
Mercury Electrode ◽  
Direct Determination ◽  
Differential Pulse ◽  
Differential Pulse Polarography ◽  
Whitening Agent ◽  
Polarographic Behaviour ◽  
Pulse Polarography ◽  
Dropping Mercury Electrode

The polarographic behaviour was studied for 6-β-D-glucopyranosyloxy-7-hydroxycoumarin, a natural compound serving as an optical whitening agent. The substance can be quantitated by tast polarography, differential pulse polarography using a conventional dropping mercury electrode, and differential pulse polarography using a static mercury drop electrode over the regions of 20-1 000, 2-1 000, and 0.2-1 000 μmol l-1, respectively. The methods developed for the quantitation of the compound were applied to its direct determination in a raw product.

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