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Published on: July 21, 2011
A new azo dye for colorimetric determination of lead(ii) ions
Sefiu Olalekan Olaleye1,2, Uzma Bibi3
1Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Ibadan, Orita UI Ibadan 200284 Nigeria solaleye5@gmail.com.
Abstract:
A new azo dye, S9b (1-amino-4-[(E)-2-(8-hydroxyquinolin-5-yl)diazen-1-yl]-9,10-dihydroanthracene-9,10-dione), was developed and evaluated as a colorimetric chemosensor for lead(ii) ions. Upon Pb2+ addition, the S9b solution color changed from rosy-brown to sandy-brown. The UV-vis spectrum of the S9b-Pb2+ complex exhibited a hyperchromic shift compared to free S9b and a bathochromic shift relative to S9b complexes with other metal ions. Optimized conditions comprised an ethanol solvent system, pH 6.0, a reaction time of 2 min, and a 2 : 1 molar ratio of S9b to Pb2+.The response of S9b was linear at Pb2+ concentrations of 3.90-9.36 μg mL-1. The calculated detection limit, quantitation limit and binding constant were 1.55 μg mL-1, 4.71 μg mL-1 and 3.07 × 104 L2 g-2, respectively. Determination of Pb2+ was not significantly affected by other interfering cations (Ag+, Co2+, Cu2+, Fe2+, Fe3+, Na+, K+, Ni2+, Hg2+, Ca2+, Zn2+, Mg2+, and Al3+). The S9b-based method demonstrated recoveries of 100.03-103.11% and relative standard deviations (RSDs) of 0.06-2.07% for Pb2+ in spiked water samples, with accuracy and precision comparable to atomic absorption spectroscopy (AAS). FTIR studies and DFT calculations indicated that Pb2+ binding to S9b occurs via the heterocyclic nitrogen and phenolic hydroxyl groups of the azo dye. The sensor demonstrated reusability following regeneration with EDTA, which dissociated the Pb2+ complex. This study highlights the potential of the anthracene-9,10-dione-based azo dye as a simple, eco-friendly, and rapid chemosensor for Pb2+ detection in aqueous systems.
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