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Trace determination of vanadium(V) using anodic adsorptive voltammetry at a glassy carbon electrode modified with multi-walled carbon nanotubes

机译:阳极吸附伏安法在多壁碳纳米管修饰的玻碳电极上痕量测定钒(V)

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A glassy carbon electrode modified with multi-walled carbon nanotubes (MWCNT) was prepared and the determination of trace amount of vanadium(V) based on the anodic adsorptive voltammetry of the vanadium-alizarin red S (ARS) complex is described for the first time. The results show that the sensitivity and the selectivity of the method are excellent. The second derivative linear scan voltammograms of the complex were recorded using a polarographic analyzer in the range from 0 to 1,000 mV (vs. SCE). It was found that the complex can be adsorbed on the surface of the electrode, yielding a peak at about 706 mV, corresponding to the oxidation of ARS in the complex. The peak current increases linearly with the V(V) concentration in the range of 6.0 nM to ∼1.0 μM (4.0 μM ARS), 2.0 μM∼10 μM (40 μM ARS) and the detection limit (at S/N = 3) was 2.0 nM (accumulation time 120 s). The method was successfully applied to the determination of trace amounts of vanadium in water samples. Keywords Multi-walled carbon nanotubes - Modified electrode - Anodic adsorptive voltammetry - Vanadium
机译:制备了用多壁碳纳米管(MWCNT)改性的玻璃碳电极,并首次描述了基于钒-茜素红S(ARS)络合物的阳极吸附伏安法测定痕量钒(V)的方法。 。结果表明,该方法灵敏度高,选择性好。使用极谱分析仪在0至1,000 mV(vs. SCE)范围内记录复合物的二阶导数线性扫描伏安图。发现该络合物可以被吸附在电极表面上,在约706mV处产生一个峰,这对应于络合物中ARS的氧化。峰值电流随着V(V)浓度在6.0 nM至〜1.0μM(4.0μMARS),2.0μM〜10μM(40μMARS)和检测极限(在S / N = 3)范围内线性增加为2.0 nM(累积时间120 s)。该方法已成功应用于水样中痕量钒的测定。关键词多壁碳纳米管修饰电极阳极吸附伏安法钒

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