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Highly Sensitive and Selective Poly(vinyl chloride)-Membrane Potentiometric Sensors Based on a Calix[4]arene Derivative for 2-Furaldehyde

A 2-furaldehyde-selective PVC-membrane electrode is designed based on the host−guest interaction between tetrabenzyl ether Calix[4]arene, as an ionophore, and a lipophilic hydrazone derivative generated in situ from reaction of 2-furaldehyde and Girard’s reagent T. At a pH of 9.2, the electrode exhi...

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Bibliographic Details
Published in:Analytical chemistry (Washington) 2009-08, Vol.81 (16), p.6789-6796
Main Authors: Shamsipur, Mojtaba, Miran Beigi, Ali Akbar, Teymouri, Mohammad, Rasoolipour, Solmaz, Asfari, Zouhair
Format: Article
Language:English
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Summary:A 2-furaldehyde-selective PVC-membrane electrode is designed based on the host−guest interaction between tetrabenzyl ether Calix[4]arene, as an ionophore, and a lipophilic hydrazone derivative generated in situ from reaction of 2-furaldehyde and Girard’s reagent T. At a pH of 9.2, the electrode exhibits a Nernstian response over the 2-furaldehyde concentration range of (5.0 × 10−5)−(1.0 × 10−1) M. The electrode has found to be chemically inert and of adequate stability with a response time of 15 s with a good reproducibility (±0.2 mV) and can be used for a long working lifetime. In order to improve the minimum detectable concentration of 2-furaldehyde, further studies have been performed using a coated graphite electrode and coated platinum and gold disks. Some analytical aspects of adsorptive square wave voltammetry have also been presented in order to elucidate the adduct formation between 2-furaldehyde and Girard’s reagent T. The interfering effects of some Na+, K+, NH4 +, formaldehyde, 5-hydroxymethyl 2-furaldehyde (HMF), excess of Girard’s reagent T and organic solvents such as isopropyl alcohol and N,N-dimethylformamide on the sensor’s response have been studied. The viability of using the electrode for the trace determination of 2-furaldehyde in several Iranian oil refinery wastewater samples is also demonstrated. The results obtained from the developed method for real samples are compared with those from UV-spectrophotometric and high-performance liquid chromatographic experiments.
ISSN:0003-2700
1520-6882
DOI:10.1021/ac900920u