People | Locations | Statistics |
---|---|---|
Naji, M. |
| |
Motta, Antonella |
| |
Aletan, Dirar |
| |
Mohamed, Tarek |
| |
Ertürk, Emre |
| |
Taccardi, Nicola |
| |
Kononenko, Denys |
| |
Petrov, R. H. | Madrid |
|
Alshaaer, Mazen | Brussels |
|
Bih, L. |
| |
Casati, R. |
| |
Muller, Hermance |
| |
Kočí, Jan | Prague |
|
Šuljagić, Marija |
| |
Kalteremidou, Kalliopi-Artemi | Brussels |
|
Azam, Siraj |
| |
Ospanova, Alyiya |
| |
Blanpain, Bart |
| |
Ali, M. A. |
| |
Popa, V. |
| |
Rančić, M. |
| |
Ollier, Nadège |
| |
Azevedo, Nuno Monteiro |
| |
Landes, Michael |
| |
Rignanese, Gian-Marco |
|
Bartroli, Jordi
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (4/4 displayed)
- 2015Improvement of the detection limit for biosensors: Advances on the optimization of biocomposite compositioncitations
- 2014Towards to the improvement of the analytical response in voltammetric sensors based on rigid compositescitations
- 2009Novel amperometric sensor based on rigid near-percolation compositecitations
- 2007Multicomponent titration of calcium + magnesium mixtures employing a potentiometric electronic-tonguecitations
Places of action
Organizations | Location | People |
---|
article
Multicomponent titration of calcium + magnesium mixtures employing a potentiometric electronic-tongue
Abstract
A fast novel potentiometric titration procedure is proposed, in which the detection system is formed by a potentiometric electronic tongue. The titration consists in a reduced number of fixed titrant additions to the sample and the recording of the potentials of an array of Ion Selective Electrodes. The obtained data matrix is entered to an Artificial Neural Network response model, previously trained to furnish concentrations of a multicomponent mixture. The principle is demonstrated with automated EDTA titration of mixtures of Ca2+ and Mg2+ at fixed pH 8.5. In this case, five 2 ml fixed volume additions plus the readings of four sensors were adequate for the resolution of the mixture. In the conditions used, titration was feasible up to 3.3 mM total ion concentration, the precision was estimated as 3.20% RSD for Ca2+ and 2.76% RSD for Mg2+ (n=5), and the detection limits 0.16 mM Ca2+ and 0.26 mM Mg2+. The procedure was applied to mineral waters and compared with reference methods (correlation=0.92 for Ca2+ and correlation=0.89 for Mg2+, n=14). Copyright © Taylor & Francis Group, LLC.