Pulse voltammetric methods of analysis

The techniques of normal and differential pulse voltammetry are presented together with equations describing these techniques. A number of specific applications for both differential and normal pulse, including determination of As III in sewage and the determination of sulphide, are presented. Advantages of amperometric titrations in eliminating ‘background’ errors are shown, with the titration of Cu II with EDTA as a specific example. The use of square-wave voltammetry, a new, rapid-pulse technique, is presented, and an application in which this technique is employed in an electrochemical high performance chromatographic detector used for nitrosamine analysis is discussed.

2015 ◽  
Vol 7 (8) ◽  
pp. 3411-3418 ◽  
Author(s):  
Gustavo Stoppa Garbellini ◽  
Romeu C. Rocha-Filho ◽  
Orlando Fatibello-Filho

A cathodically pretreated boron-doped diamond electrode is successfully used to determine ciprofloxacin (CIP) by differential pulse voltammetry and to infer the type of binding of CIP to DNA by square-wave voltammetry.


2005 ◽  
Vol 70 (3) ◽  
pp. 292-304 ◽  
Author(s):  
Natalija German ◽  
Saulius Armalis ◽  
Jiří Zima ◽  
Jiří Barek

Square wave voltammetry and differential pulse voltammetry have been used for the determination of 2-acetamidofluorene and fluoren-9-ol using carbon paste electrodes, following the study of the influence of the carbon paste composition on the voltammetric signals of the analytes. The methods are based on the oxidation of the above compounds and they include adsorptive accumulation of the analyte on the surface of the working electrode. The limit of detection was 1 μmol l-1for fluoren-9-ol in a medium of 0.1 M H2SO4, and 40 nmol l-1for 2-acetamidofluorene in Britton-Robinson buffer (pH 7).


2019 ◽  
Vol 15 (6) ◽  
pp. 648-655 ◽  
Author(s):  
Shengzhong Rong ◽  
Deng Pan ◽  
Xuehui Li ◽  
Mucong Gao ◽  
Hongwei Yu ◽  
...  

Background: 8-Hydroxy-2’-deoxyguanosine (8-OHdG) has been regarded as a typical stable biomarker of DNA oxidative damage, and its level is one of the criteria for early diagnosis of various diseases. Considering the significance of 8-OhdG, various analytical techniques have been used for assaying 8-OHdG but all of them suffer from basic limitations like highly expensive instrumentation, large amount of sample requirement, complicated sample pre-treatment, tedious and time-consuming procedures etc. However, electroanalytical sensors provide a faster, easy and sensitive means of analyzing. Methods: The chitosan (CS) film provided the high electrode activity and stability which is required for detecting 8-OHdG though direct electrochemical oxidation. Zirconia was employed because it has some unique properties, such as high redox activity and selectivity etc. High-performance composite was easily detected by differential pulse voltammetry at a working voltage of 0. 51 V (vs. Ag/AgCl). A rapid and sensitive electrochemical sensor based on CS and metal oxide nanocrystalline for the determination of 8-OHdG was established. Results: Under optimized experimental conditions, the peak currents of differential pulse voltammetry increased as the concentrations of 8-OHdG increased from 10 to 200 ng·mL-1. The detection limit was 3.67 ng·mL-1 which was calculated by the S/N ratio of 3. The recoveries of the real spiked samples are in the range between 93.2 to 105.3%. Conclusion: The electrochemical sensor for direct 8-OHdG determination using a new CS/zirconia composite for GCE modification was developed and showed excellent reproducibility, stability and sensitivity for the specific determination of 8-OHdG in real urine specimen.


1986 ◽  
Vol 51 (11) ◽  
pp. 2466-2472 ◽  
Author(s):  
Jiří Barek ◽  
Antonín Berka ◽  
Ludmila Dempírová ◽  
Jiří Zima

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.


1991 ◽  
Vol 56 (3) ◽  
pp. 595-601 ◽  
Author(s):  
Jiří Barek ◽  
Gulamustafa Malik ◽  
Jiří Zima

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.


2021 ◽  
Author(s):  
Yan Jin ◽  
Tong QI ◽  
Yuqing Ge ◽  
Jin Chen ◽  
Li juan Liang ◽  
...  

In this paper, ultrasensitive electrochemical determination of phosphate in water is achieved by hydrophilic TiO2 modified glassy carbon electrodes for the first time. Differential pulse voltammetry (DPV) method is proposed...


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