Amino-functionalized mesoporous silica modified glassy carbon electrode for ultra-trace copper(II) determination

被引:42
作者
Dai, Xingxin [1 ]
Qiu, Fagui [3 ]
Zhou, Xuan [1 ]
Long, Yumei [1 ,2 ]
Li, Weifeng [1 ]
Tu, Yifeng [1 ]
机构
[1] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Jiangsu, Peoples R China
[2] Key Lab Hlth Chem & Mol Diag Suzhou, Suzhou, Peoples R China
[3] Jilin Univ, Dept Quartermaster Engn, Changchun 130062, Peoples R China
基金
中国国家自然科学基金;
关键词
Mesoporous silica; Amino-functionalized; Sensor; Anodic stripping voltammetry; Copper; CONDENSATION; CADMIUM; METALS; MCM-41;
D O I
10.1016/j.aca.2014.08.002
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This paper described a facile and direct electrochemical method for the determination of ultra-trace Cu2+ by employing amino-functionalized mesoporous silica (NH2-MCM-41) as enhanced sensing platform. NH2-MCM-41 was prepared by using a post-grafting process and characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and fourier transform infrared (FTIR) spectroscopy. NH2-MCM-41 modified glassy carbon (GC) electrode showed higher sensitivity for anodic stripping voltammetric (ASV) detection of Cu2+ than that of MCM-41 modified one. The high sensitivity was attributed to synergistic effect between MCM-41 and amino-group, in which the high surface area and special mesoporous morphology of MCM-41 can cause strong physical absorption, and amino-groups are able to chelate copper ions. Some important parameters influencing the sensor response were optimized. Under optimum experimental conditions the sensor linearly responded to Cu2+ concentration in the range from 5 to 1000 ng L (1) with a detection limit of 0.9 ng L (1) (S/N = 3). Moreover, the sensor possessed good stability and electrode renewability. In the end, the proposed sensor was applied for determining Cu2+ in real samples and the accuracy of the results were comparable to those obtained by inductively coupled plasma optical emission spectrometry (ICP-OES) method. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:25 / 31
页数:7
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