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Sensitive and Simple Electrochemical Detection of Lead(II) with Carbon Ionic Liquid Electrode
Author(s) -
Liu HeJian,
Qu LiNing,
Hu Song,
Zhan TianRong,
Zhao ChaoZhi,
Sun Wei
Publication year - 2010
Publication title -
journal of the chinese chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.329
H-Index - 45
eISSN - 2192-6549
pISSN - 0009-4536
DOI - 10.1002/jccs.201000202
Subject(s) - chemistry , detection limit , ionic liquid , anodic stripping voltammetry , stripping (fiber) , voltammetry , electrochemistry , extraction (chemistry) , analytical chemistry (journal) , electrode , dielectric spectroscopy , inorganic chemistry , cyclic voltammetry , buffer solution , chromatography , catalysis , biochemistry , electrical engineering , engineering
In this paper a carbon ionic liquid electrode (CILE) was fabricated by using ionic liquid 1‐ethyl‐3‐methylimidazolium ethylsulphate ([EMIM]EtOSO 3 ) as the modifier and further used as the working electrode for the sensitive anodic stripping voltammetric detection of Pb 2+ . The characteristics of the CILE were investigated by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). In pH 4.5 NaAc‐HAc buffer Pb 2+ was accumulated on the surface of CILE due to the extraction effect of IL and reduced at a negative potential (‐1.20 V). Then the reduced Pb was oxidized by differential pulse anodic stripping voltammetry with an obvious stripping peak appeared at −0.67 V. Under the optimal conditions Pb 2+ could be detected in the concentration range from 1.0 × 10 −8 mol/L to 1.0 × 10 −6 mol/L with the linear regression equation as I p (μA) = −0.103 C (μmol/L) + 0.0376 (γ = 0.999) and the detection limit as 3.0 × l0 −9 mol/L (3σ). Interferences from other metal ions were investigated and Cd 2+ could be simultaneously detected in the mixture solution. The proposed method was further applied to the trace levels of Pb 2+ detection in water samples with satisfactory results.