Voltammetric determination of trace amounts of aluminium

1989 ◽  
Vol 54 (2) ◽  
pp. 370-374 ◽  
Author(s):  
Věra Stará ◽  
Miloslav Kopanica
Keyword(s):  
Linear Dependence ◽  
Differential Pulse ◽  
Hanging Mercury Drop Electrode ◽  
Pulse Technique ◽  
Aluminium Concentration ◽  
Lead And Cadmium ◽  
Effect Of Copper ◽  
Alizarin Violet ◽  
Copper Lead

Aluminium is determined voltammetrically in the form of the aluminium complex with Acid Alizarin Violet N in an acetate buffer of pH 5.2 using a hanging mercury drop electrode and the d.c. or differential pulse technique. A linear dependence between the peak current and the aluminium concentration was obtained in the range from 2.10-8 to 5.10-6 mol l-1. The interfering effect of copper, lead and cadmium is eliminated by the auxiliary complex forming reagent-glycine.

scholarly journals The Effect of Salinity on the Release of Copper (Cu), Lead (Pb) And Zinc (Zn) from Tailing

2010 ◽  
Vol 1 (1) ◽  
pp. 16-22
Author(s):  
Apriani Sulu Parubak ◽  
Eko Sugiharto ◽  
Mudjiran Mudjiran
Keyword(s):  
Limit Of Detection ◽  
Anodic Stripping Voltammetry ◽  
Stripping Voltammetry ◽  
Differential Pulse ◽  
Hanging Mercury Drop Electrode ◽  
Lead And Zinc ◽  
Anodic Stripping ◽  
Determination Of Copper ◽  
Copper Lead

The effects of salinity on the release of copper (Cu), lead (Pb) and zinc (Zn) in tailing sediment have been studied by stripping voltammetry. The purpose of the research is to know the effect of salinity on the release of metals with certain pH, conductivity and variety of metals. Simultaneous determination of copper, lead and zinc in tailing was done by Differential Pulse Anodic Stripping Voltammetry (DPASV) onto hanging mercury drop electrode (HMDE) and nitric acid 65% as support electrolyte. The limit of detection for this method 0.60 µg/L, 0.150 µg/L and 0.238 µg/L for copper, lead and iMc respectively. The stripping solution of 300/00 salinity with pH= 7.85, conductivity= 46.62 mS/cm gives the amounts of released metals as follows :14.867 µg/L Cu, 0.976 µg/L Pb and 6.224 µg/L Zn. These results are higher as compared with the results from 15 0/00 salinity with pH= 7.66, conductivity= 23.22 mS/cm that give released metals of Cu= 7.988 µg/L, Pb= 0.311 µg/L and Zn= 4.699 µg/L. the results from ANOVA suggest that this is due to different in salinity of the solution. It also found that the conductivity does not give any effect. It can be concluded that the higher salinity will that give higher concentration or released metals.

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.

The voltammetric determination of 4-nitrobiphenyl

1991 ◽  
Vol 56 (3) ◽  
pp. 595-601 ◽  
Author(s):  
Jiří Barek ◽  
Gulamustafa Malik ◽  
Jiří Zima
Keyword(s):  
Differential Pulse Voltammetry ◽  
Differential Pulse ◽  
Voltammetric Determination ◽  
Hanging Mercury Drop Electrode ◽  
Optimum Conditions ◽  
Mercury Drop Electrode ◽  
Working Electrode ◽  
Pulse Voltammetry ◽  
Unstirred Solution

Optimum conditions were found for the determination of 4-nitrobiphenyl by fast scan differential pulse voltammetry at a hanging mercury drop electrode in the concentration range 1 . 10-5 to 2 . 10-7 mol l-1. A further increase in sensitivity was attained by adsorptive accumulation of this substance on the surface of the working electrode, permitting determination in the concentration range (2 – 10) . 10-8 mol l-1 with one minute accumulation of the substance in unstirred solution or (2 – 10) . 10-9 mol l-1 with three-minute accumulation in stirred solution. Linear scan voltammetry can be used to determine 4-nitrobiphenyl in the concentration range (2 – 10) . 10-9 mol l-1 with five-minute accumulation in stirred solution, with the advantage of a smoother baseline and smaller interference from substances that yield only tensametric peaks.

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