Differential pulse anodic stripping voltammetric determination of traces of copper with a tobramycin-Nafion modified electrode
被引:13
|
作者:
Li, NB
论文数: 0引用数: 0
h-index: 0
机构:
SW China Normal Univ, Sch Chem & Chem Engn, Chongqing 400715, Peoples R ChinaSW China Normal Univ, Sch Chem & Chem Engn, Chongqing 400715, Peoples R China
Li, NB
[1
]
Luo, HQ
论文数: 0引用数: 0
h-index: 0
机构:SW China Normal Univ, Sch Chem & Chem Engn, Chongqing 400715, Peoples R China
Luo, HQ
Chen, GN
论文数: 0引用数: 0
h-index: 0
机构:SW China Normal Univ, Sch Chem & Chem Engn, Chongqing 400715, Peoples R China
Chen, GN
机构:
[1] SW China Normal Univ, Sch Chem & Chem Engn, Chongqing 400715, Peoples R China
[2] Fuzhou Univ, Dept Chem, Fujian 350002, Peoples R China
A Nafion-modified glassy carbon electrode incorporated with tobramycin for the voltammetric stripping determination of Cu2+ has been explored. The electrode was fabricated by tobramycin containing Nafion on the glassy carbon electrode surface. The modified electrode exhibited a significantly increased sensitivity and selectivity for Cu2+ compared with a bare glassy carbon electrode and the Nafion modified electrode. Cu2+ was accumulated in HAc-NaAc buffer (pH 4.6) at a potential of -0.6 V (vs. SCE) for 300 s and then determined by differential pulse anodic stripping voltammetry. The effects of various parameters, such as the mass of Nafion, the concentration of tobramycin, the pH of the medium, the accumulation potential, the accumulation time and the scan rate, were investigated. Under the optimum conditions, a linear calibration graph was obtained in the concentration range of 1.0 x 10(-9) to 5.0 x 10(-7) mol l(-1) with a correlation coefficient of 0.9971. The relative standard deviations for eight successive determinations were 4.3 and 2.9% for 1.0 x 10(-8) and 2.0 x 10(-7) mol l(-1) Cu2+, respectively. The detection limit (three times signal to noise) was 5.0 x 10(-10) mol l(-1). A study of interfering substances was also performed, and the method was applied to the direct determination of copper in water samples, and also in analytical reagent-grade salts with satisfactory results.