Abstract
Differential pulse voltammetry with a glassy carbon electrode was used for the determination of trace amounts of 4-nitroaniline in Britton-Robinson buffer at pH 2.0 as an optimal base electrolyte. 4-Nitroaniline can be determined by differential pulse voltammetry directly using either its electrochemical oxidation or reduction. The calibration curve was measured for both reactions in the same concentration range from 2 to 100 μmol dm-3. The calculated limits of detection and quantification are 0.2 and 0.7 μmol dm-3 (RSD 6.62 % and R 2 = 0.9906 for n = 5) for cathodic reduction and 0.3 and 1.0 μmol dm-3 (RSD 7.62 % and R 2 = 0.9995 for n = 5) for anodic oxidation.
| Original language | English |
|---|---|
| Pages (from-to) | 111-118 |
| Number of pages | 8 |
| Journal | Monatshefte fur Chemie |
| Volume | 147 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 1 Jan 2016 |
| Externally published | Yes |
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Keywords
- Nitro aromatic compounds
- Oxidations
- Reductions
- Voltammetry
ASJC Scopus subject areas
- Chemistry(all)
Cite this
Differential pulse voltammetric determination of 4-nitroaniline using a glassy carbon electrode : Comparative study between cathodic and anodic quantification. / Pfeifer, Rene; Tamiasso-Martinhon, Priscila; Sousa, Célia; Moreira, Josino Costa; Do Nascimento, Marco Antônio Chaer; Barek, Jíři.
In: Monatshefte fur Chemie, Vol. 147, No. 1, 01.01.2016, p. 111-118.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Differential pulse voltammetric determination of 4-nitroaniline using a glassy carbon electrode
T2 - Comparative study between cathodic and anodic quantification
AU - Pfeifer, Rene
AU - Tamiasso-Martinhon, Priscila
AU - Sousa, Célia
AU - Moreira, Josino Costa
AU - Do Nascimento, Marco Antônio Chaer
AU - Barek, Jíři
PY - 2016/1/1
Y1 - 2016/1/1
N2 - Differential pulse voltammetry with a glassy carbon electrode was used for the determination of trace amounts of 4-nitroaniline in Britton-Robinson buffer at pH 2.0 as an optimal base electrolyte. 4-Nitroaniline can be determined by differential pulse voltammetry directly using either its electrochemical oxidation or reduction. The calibration curve was measured for both reactions in the same concentration range from 2 to 100 μmol dm-3. The calculated limits of detection and quantification are 0.2 and 0.7 μmol dm-3 (RSD 6.62 % and R 2 = 0.9906 for n = 5) for cathodic reduction and 0.3 and 1.0 μmol dm-3 (RSD 7.62 % and R 2 = 0.9995 for n = 5) for anodic oxidation.
AB - Differential pulse voltammetry with a glassy carbon electrode was used for the determination of trace amounts of 4-nitroaniline in Britton-Robinson buffer at pH 2.0 as an optimal base electrolyte. 4-Nitroaniline can be determined by differential pulse voltammetry directly using either its electrochemical oxidation or reduction. The calibration curve was measured for both reactions in the same concentration range from 2 to 100 μmol dm-3. The calculated limits of detection and quantification are 0.2 and 0.7 μmol dm-3 (RSD 6.62 % and R 2 = 0.9906 for n = 5) for cathodic reduction and 0.3 and 1.0 μmol dm-3 (RSD 7.62 % and R 2 = 0.9995 for n = 5) for anodic oxidation.
KW - Nitro aromatic compounds
KW - Oxidations
KW - Reductions
KW - Voltammetry
UR - http://www.scopus.com/inward/record.url?scp=84952792083&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84952792083&partnerID=8YFLogxK
U2 - 10.1007/s00706-015-1596-3
DO - 10.1007/s00706-015-1596-3
M3 - Article
AN - SCOPUS:84952792083
VL - 147
SP - 111
EP - 118
JO - Monatshefte fur Chemie
JF - Monatshefte fur Chemie
SN - 0026-9247
IS - 1
ER -