Issue 12, 2006

Voltammetric analysis of europium at screen-printed electrodes modified with salicylamide self-assembled on mesoporous silica

Abstract

Mercury-free sensors for europium (Eu3+) assay based on the chemical modification of screen-printed carbon electrodes (SPCEs) with self-assembled salicylamide on mesoporous silica (Sal-SAMMS) have been developed. The preconcentration of Eu3+ at SAMMS-based sensors utilizes the binding affinity of the salicylamide and Eu3+, accomplished at open circuit potential without electrolyte and solution de-gassing. Optimal Eu detection was obtained after 3–5 min preconcentration in Eu solution (pH 2–6), electrolysis at −0.9 V for 60 s in a new medium (0.1–0.2 M NH4Cl, pH 3.5), followed by a square-wave voltammetric detection of Eu in the same electrolyte. Attributed to the strong covalent bonding of the functional groups on mesoporous silica and silane cross-linking, the SAMMS-modified SPCEs with a built-in 3-electrode system can be re-used for tens of measurements with minimal degradation, enabling the establishment of the calibration curve and lowering the costs. A linear calibration curve was found in the range of 75 to at least 500 ppb Eu3+ after 5 min preconcentration. The experimental detection limit was 10 ppb after 10 min preconcentration, which can be improved with increased preconcentration time. Reproducibility (% RSD) of 100 ppb Eu2+ was 10% for a single sensor and 10% for 5 sensors, which can be improved through the precision of sensor manufacturing, in which SAMMS modification can be made in-situ.

Graphical abstract: Voltammetric analysis of europium at screen-printed electrodes modified with salicylamide self-assembled on mesoporous silica

Article information

Article type
Paper
Submitted
29 Jun 2006
Accepted
29 Sep 2006
First published
11 Oct 2006

Analyst, 2006,131, 1342-1346

Voltammetric analysis of europium at screen-printed electrodes modified with salicylamide self-assembled on mesoporous silica

W. Yantasee, G. E. Fryxell and Y. Lin, Analyst, 2006, 131, 1342 DOI: 10.1039/B609211J

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