Premium
Construction and characterization of nano iron complex ionophore for electrochemical determination of Fe(III) in pure and various real water samples
Author(s) -
Ali Tamer Awad,
Mahmoud Walaa H.,
Mohamed Gehad G.
Publication year - 2019
Publication title -
applied organometallic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.53
H-Index - 71
eISSN - 1099-0739
pISSN - 0268-2605
DOI - 10.1002/aoc.5206
Subject(s) - electrode , chemistry , detection limit , electrochemistry , ionophore , ion , analytical chemistry (journal) , carbon paste electrode , metal ions in aqueous solution , characterization (materials science) , nanoparticle , nanotechnology , materials science , cyclic voltammetry , membrane , chromatography , organic chemistry , biochemistry
Electrochemical methods represent an important class of widely used techniques for the detection of metal ions. The unique chemical and physical properties of nanoparticles make them extremely suitable for designing new and improved sensing devices, especially electrochemical sensors and biosensors. This study focused on the synthesis of a nano‐Fe(III)–Sud complex and its characterization using various spectroscopic and analytical tools, optimized using the density functional theory method, screened for antibacterial activity and evaluated for possible binding to DNA using molecular docking study. Proceeding from the collected information, nano‐Fe(III)–Sud was used further for constructing carbon paste and screen‐printed ion‐selective electrodes. The proposed sensors were successfully applied for the determination of Fe(III) ions in various real and environmental water samples. Some texture analyses of the electrode surface were conducted using atomic force microscopy. At optimum values of various conditions, the proposed electrodes responded towards Fe(III) ions linearly in the range 2.5 × 10 −9 –1 × 10 −2 and 1.0 × 10 −8 –1 × 10 −2 M with slope of 19.73 ± 0.82 and 18.57 ± 0.32 mV decade −1 of Fe(III) ion concentration and detection limit of 2.5 × 10 −9 and 1.0 × 10 −8 M for Fe(III)–Sud‐SPE (electrode I) and Fe(III)–Sud‐CPE (electrode II), respectively. The electrode response is independent of pH in the range 2.0–7.0 and 2.5–7.0, with a fast response time (4 and 7 s) at 25°C for electrode I and electrode II, respectively. Moreover, the electrodes also showed high selectivity and long lifetime (more than 6 and 3 months for electrode I and electrode II, respectively). The electrodes showed good selectivity for Fe(III) ions among a wide variety of metal ions. The results obtained compared well with those obtained using atomic absorption spectrometry.