Abstract

Langmuir isotherms of poly(o-ethoxyaniline) (PEOA) were investigated at two different subphases containing deionized water at pH 3 using HCl. The doping during the monolayer formation was observed to be an essential condition for obtaining the high quality of the Langmuir film. The PEOA Langmuir-Schaefer (LS) films were manufactured, and linearity in the deposition process was verified by using UV-visible, quartz crystal microbalance, current–voltage, atomic force microscopy (AFM) and cyclic voltammetric (CV) techniques, respectively. The regularity of PEOA LS films could be well maintained by either dedoping the films in NaOH or redoping in 1 M HCl. The linear variation in frequency change as well as systematic doping in PEOA LS films was studied by quartz crystal microbalance measurements. AFM study depicted that the LS films were composed of regular grains of 23±5 nm in diameter. The PEOA LS films showed a conductivity value of 0.001 S/cm. The electrochemical surveyings of PEOA LS films revealed a switching halftime of 300 ms. The presence of heavy metallic ions in the solution revealed well-separated oxidation peak potentials in cyclic voltammetric measurements. This work presents the first evidence in recognition of heavy metallic ions in a solution using PEOA LS films by differential pulse voltammetric (DPV) technique. The DPV study on PEOA LS films in metallic-ions-containing solution showed the distinctive oxidation potentials at 370 (Fe3+), 170 (Hg2+), −130 (Cu2+), −512 (Pb2+) and −720 (Cd2+) mV, respectively. The Pb2+ ions concentration between 0.1 and 5 ppm was detected using PEOA LS films.

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