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Determination of Trace Amounts of Sulfamethizole Using a Multi-Walled Carbon Nanotube Modified Electrode: Application of Experimental Design in Voltammetric Studies

机译:多壁碳纳米管修饰电极测定痕量的磺胺甲基咪唑:实验设计在伏安研究中的应用

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摘要

The present paper is the first report for the simultaneous investigation of various factors affecting the oxidation peak currents of sulfamethizole (SM) in a 0.20 M Britton-Robinson (B-R) buffer solution. Experimental factors (pH, multiwalled carbon nanotube amount, scan rate, step potential, and modulation amplitude) on voltammetric determination of SM were optimized simultaneously by a central composite rotatable design (CCRD). Then, in the optimized conditions, differential pulse voltammetry (DPV) was applied for selective determination of SM at the surface of a multi-walled carbon nanotube modified carbon paste electrode (MWCNT/CPE).The modified electrode showed enhanced effect on the oxidation peak current of SM. In these conditions the linear dynamic range for SM was from 0.10 up to 131.94 μM and the detection limit was found to be 14.31 nM. The characterization of MWCNT/CPE was carried out bycyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). Also, linear sweep voltammetry (LSV) and chronocoulometry of SM were studied. Using these techniques, the diffusion coefficient (D = 4.91 × 10~(-5) cm~2 s~(-1)) and the kinetic parameters such as the electron transfer coefficient (α = 0.79) and exchange current density (j0 = 2.78 × 10~(-12) μA cm~(-2)) for SM were calculated. The proposed method was then successfully applied to the determination of SM in plasma samples.
机译:本文是同时研究影响0.20 M Britton-Robinson(B-R)缓冲溶液中磺胺甲二唑(SM)氧化峰电流的各种因素的第一份报告。通过中央复合可旋转设计(CCRD)同时优化了关于伏安法测定SM的实验因素(pH,多壁碳纳米管数量,扫描速率,步进电势和调制幅度)。然后,在优化条件下,采用差示脉冲伏安法(DPV)选择性测定多壁碳纳米管修饰碳糊电极(MWCNT / CPE)表面的SM,修饰电极对氧化峰的影响增强。当前的SM。在这些条件下,SM的线性动态范围为0.10至131.94μM,检测极限为14.31 nM。 MWCNT / CPE的表征通过循环伏安法(CV)和电化学阻抗谱(EIS)进行。此外,还研究了线性扫描伏安法(LSV)和SM计时库仑法。使用这些技术,扩散系数(D = 4.91×10〜(-5)cm〜2 s〜(-1))和动力学参数,例如电子转移系数(α= 0.79)和交换电流密度(j0 =计算出SM的2.78×10〜(-12)μAcm〜(-2))。该方法成功地应用于血浆样品中SM的测定。

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