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使用多壁碳纳米管/钴酞菁修饰电极直接电化学测定西维因。

Direct electrochemical determination of carbaryl using a multi-walled carbon nanotube/cobalt phthalocyanine modified electrode.

作者信息

Moraes Fernando C, Mascaro Lucia H, Machado Sergio A S, Brett Christopher M A

机构信息

Departamento de Química, Universidade Federal de São Carlos, São Carlos, SP, Brazil.

出版信息

Talanta. 2009 Oct 15;79(5):1406-11. doi: 10.1016/j.talanta.2009.06.013. Epub 2009 Jun 12.

Abstract

The electrochemical detection of carbaryl at low potentials, in order to avoid matrix interferences, is an important challenge. This study describes the development, electrochemical characterization and utilization of a glassy carbon (GC) electrode modified with multi-wall carbon nanotubes (MWCNT) plus cobalt phthalocyanine (CoPc) for the quantitative determination of carbaryl in natural waters. The surface morphology was examined by scanning electron microscopy, enhanced sensitivity was observed with respect to bare glassy carbon and electrocatalytic effects reduced the oxidation potential to +0.80 V vs. SCE in acetate buffer solution at pH 4.0. Electrochemical impedance spectroscopy was used to estimate the rate constant of the oxidation process and square-wave voltammetry to investigate the effect of electrolyte pH. Square-wave voltammetry in acetate buffer solution at pH 4.0, allowed the development of a method to determine carbaryl, without any previous step of extraction, clean-up, or derivatization, in the range of 0.33-6.61 micromol L(-1), with a detection limit of 5.46+/-0.02 nmol L(-1) (1.09+/-0.02 microg L(-1)) in water. Natural water samples spiked with carbaryl and without any purification step were successfully analyzed by the standard addition method using the GC/MWCNT/CoPc film electrode.

摘要

为避免基质干扰,在低电位下对西维因进行电化学检测是一项重大挑战。本研究描述了一种用多壁碳纳米管(MWCNT)加钴酞菁(CoPc)修饰的玻碳(GC)电极的研制、电化学表征及其在天然水中西维因定量测定中的应用。通过扫描电子显微镜对表面形态进行了检测,相对于裸玻碳电极,观察到灵敏度有所提高,并且电催化效应使在pH 4.0的醋酸盐缓冲溶液中相对于饱和甘汞电极(SCE)的氧化电位降低至+0.80 V。用电化学阻抗谱估算氧化过程的速率常数,并用方波伏安法研究电解质pH的影响。在pH 4.0的醋酸盐缓冲溶液中进行方波伏安法测定,无需任何萃取、净化或衍生化的前期步骤,即可建立一种测定西维因的方法,其测定范围为0.33 - 6.61 μmol L⁻¹,水中的检测限为5.46±0.02 nmol L⁻¹(1.09±0.02 μg L⁻¹)。通过标准加入法,使用GC/MWCNT/CoPc薄膜电极成功分析了添加了西维因且未经过任何净化步骤的天然水样。

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