Determination of tetramethrin (neo-pynamin) by differential pulse voltammetry with a carbon paste electrode modified with sepiolite

1989 ◽  
Vol 334 (6) ◽  
pp. 550-553 ◽  
Author(s):  
Pedro Hernandez ◽  
Jose Vicente ◽  
Lucas Hernandez
Keyword(s):  
Differential Pulse Voltammetry ◽  
Carbon Paste Electrode ◽  
Differential Pulse ◽  
Carbon Paste ◽  
Pulse Voltammetry ◽  
Paste Electrode

DIFFERENTIAL PULSE VOLTAMMETRY FOR DETERMINATION OF PARACETAMOL AT A PUMICE MIXED CARBON PASTE ELECTRODE

2001 ◽  
Vol 34 (15) ◽  
pp. 2747-2759 ◽  
Author(s):  
Chengyin Wang ◽  
Xiaoya Hu ◽  
Zongzhou Leng ◽  
Gongjun Yang ◽  
Gendi Jin
Keyword(s):  
Differential Pulse Voltammetry ◽  
Carbon Paste Electrode ◽  
Differential Pulse ◽  
Carbon Paste ◽  
Pulse Voltammetry ◽  
Paste Electrode

A graphene/ionic liquid modified selenium-doped carbon paste electrode for determination of copper and antimony

2016 ◽  
Vol 8 (5) ◽  
pp. 1120-1126 ◽  
Author(s):  
Rong Liu ◽  
Cunxi Lei ◽  
Tongsheng Zhong ◽  
Liping Long ◽  
Zhaoyang Wu ◽  
...  
Keyword(s):  
Ionic Liquid ◽  
Differential Pulse Voltammetry ◽  
Carbon Paste Electrode ◽  
Differential Pulse ◽  
Carbon Paste ◽  
Pulse Voltammetry ◽  
Paste Electrode ◽  
Determination Of Copper

A graphene (GN) and ionic liquid (IL) modified selenium-doped carbon paste electrode (GN/IL/Se/CPE) was established to simultaneously determine trace Cu(ii) and Sb(iii) by differential pulse voltammetry (DPV).

scholarly journals Electrochemical Behavior and Voltammetric Determination of a Manganese(II) Complex at a Carbon Paste Electrode

2016 ◽  
Vol 11 ◽  
pp. ACI.S32150 ◽  
Author(s):  
Sophia Karastogianni ◽  
Stella Girousi
Keyword(s):  
Carboxylic Acid ◽  
Differential Pulse Voltammetry ◽  
Carbon Paste Electrode ◽  
Electrochemical Behavior ◽  
Differential Pulse ◽  
Carbon Paste ◽  
Oxidation Reduction ◽  
Pulse Voltammetry ◽  
Paste Electrode

Investigation of the electrochemical behavior using cyclic voltammetry and detection of [Mn2+(thiophenyl-2-carboxylic acid)2 (triethanolamine)] with adsorptive stripping differential pulse voltammetry. The electrochemical behavior of a manganese(II) complex [Mn2+(thiophenyl-2-carboxylic acid)2(triethanolamine)] (A) was investigated using cyclic and differential pulse voltammetry in an acetate buffer of pH 4.6 at a carbon paste electrode. Further, an oxidation-reduction mechanism was proposed. Meanwhile, an adsorptive stripping differential pulse voltammetric method was developed for the determination of manganese(II) complex.

Determination of flunitrazepam by differential-pulse voltammetry using a bentonite-modified carbon paste electrode

The Analyst ◽  
1988 ◽  
Vol 113 (11) ◽  
pp. 1719-1722 ◽  
Author(s):  
Lucas Hernández ◽  
Pedro Hernández ◽  
Manuel H. Blanco ◽  
Encarnacion Lorenzo ◽  
Engracia Alda
Keyword(s):  
Differential Pulse Voltammetry ◽  
Carbon Paste Electrode ◽  
Differential Pulse ◽  
Modified Carbon Paste Electrode ◽  
Carbon Paste ◽  
Pulse Voltammetry ◽  
Paste Electrode

scholarly journals Development of a Carbon Paste Electrode Containing Benzo-15-Crown-5 for Trace Determination of the Uranyl Ion by Using a Voltammetric Technique

2009 ◽  
Vol 92 (1) ◽  
pp. 241-247 ◽  
Author(s):  
Sunil K Agrahari ◽  
Sangita D Kumar ◽  
Ashwini K Srivastava
Keyword(s):  
Detection Limit ◽  
Differential Pulse Voltammetry ◽  
Modified Electrode ◽  
Carbon Paste Electrode ◽  
Electrochemical Impedance ◽  
Differential Pulse ◽  
Carbon Paste ◽  
Pulse Voltammetry ◽  
Paste Electrode

Abstract The interaction of macrocyclic compounds like crown ethers and UO22+ has been studied by electrochemical methods. A modified carbon paste electrode incorporating benzo-15-crown-5 (B15C5) was used to evaluate the electron transfer reaction of UO22+ by cyclic voltammetry, differential pulse voltammetry, and electrochemical impedance spectroscopy. Electrochemical impedance studies showed that charge transfer resistance was less for the B15C5-modified electrode than for the plain carbon paste electrode (PCPE). On the basis of these observations, a UO22+-sensitive crown ether chemically modified electrode (CME) for trace analysis was fabricated and investigated in aqueous solutions. It was found that a 5 B15C5CME for UO22+ showed a better voltammetric response than did the PCPE. UO22+ could be quantified at sub-μg/mL levels by differential pulse voltammetry with a detection limit of 0.03 μg/mL. By differential pulse adsorptive stripping voltammetry, UO22+ could be quantified in the working range of 0.002-0.2 μg/mL, with a detection limit of 1.1 μg/L. Simultaneous determination of UO22+, Pb2+, and Cd2+ was possible. The method was successfully applied to the determination of UO22+ in synthetic, as well as real, samples; the results were found to be comparable to those obtained by inductively coupled plasma-atomic emission spectroscopy.

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