scholarly journals In-situ Measurement of Sm3+ Concentration in NaCl-2CsCl Molten Salt by Differential Pulse Voltammetry.

2003 ◽  
Vol 2 (4) ◽  
pp. 580-584
Author(s):  
Takayuki NAGAI
Keyword(s):  
Differential Pulse Voltammetry ◽  
Molten Salt ◽  
Differential Pulse ◽  
In Situ Measurement ◽  
Pulse Voltammetry

Electrically stimulated liquid phase microextraction combined with differential pulse voltammetry: a new and efficient design for in situ determination of clozapine from complicated matrices

RSC Advances ◽  
2016 ◽  
Vol 6 (16) ◽  
pp. 12943-12952 ◽  
Author(s):  
Ahmad Rouhollahi ◽  
Masoomeh Kouchaki ◽  
Shahram Seidi
Keyword(s):  
Liquid Phase ◽  
Differential Pulse Voltammetry ◽  
Differential Pulse ◽  
Efficient Design ◽  
Liquid Phase Microextraction ◽  
Electromembrane Extraction ◽  
Pulse Voltammetry ◽  
Complicated Matrices

Electromembrane extraction combined with differential pulse voltammetry for in situ determination of clozapine from complicated matrices.

Investigations On The Binding Of Mercury Ions To Albumins Employing Differential Pulse Voltammetry

2003 ◽  
Vol 10 (2) ◽  
pp. 155-164 ◽  
Author(s):  
Clarissa Pires de Castro ◽  
Jurandir SouzaDe ◽  
Carlos Bloch Jr
Keyword(s):  
Differential Pulse Voltammetry ◽  
Differential Pulse ◽  
Mercury Ions ◽  
Pulse Voltammetry

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 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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