Electrochemical determination of para-nitrophenol at apatite-modified carbon paste electrode: Application in river water samples

被引:158
|
作者
El Mhammedi, M. A. [1 ]
Achak, M. [2 ]
Bakasse, M. [3 ]
Chtaini, A. [1 ]
机构
[1] Univ Sultan Moulay Slimane, Equipe Electrochim & Mat Inorgan, Fac Sci & Tech, Beni Mellal, Morocco
[2] Univ Cadi Ayyad, Fac Sci Semlalia, Lab Hydrobiol & Algol, Marrakech, Morocco
[3] Univ Chouaib Doukkali, Fac Sci, Equipe Anal Micropolluants Organ, El Jadida, Morocco
关键词
Carbon paste electrode; Hydroxyapatite; para-Nitrophenol; Square wave voltammetry; PERFORMANCE LIQUID-CHROMATOGRAPHY; VOLTAMMETRIC DETERMINATION; P-NITROPHENOL; 4-NITROPHENOL; PHENOLS;
D O I
10.1016/j.jhazmat.2008.06.126
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The behavior of a modified carbon paste electrode (CPE) for para-nitrophenol detection by cyclic and square wave voltammetry (SWV) was studied. The electrode was built by incorporating the hydroxyapatite (HAP) to carbon paste. The overall analysis involved a two-step procedure: an accumulation step at open circuit, followed by medium exchange to a pure electrolyte solution for the voltammetric quantification. During the preconcentration step, para-nitrophenol was adsorbed onto hydroxyapatite surface. The influence of various experimental parameters on the HAP-CPE response was investigated (i.e. pH, carbon paste composition, accumulation time). Under the optimized conditions, the reduction peak shows that the peak height was found to be directly proportional to the para-nitrophenol concentration in the range comprised between 2 x 10(-7) mol L-1 and 1 x 10(-4) mol L-1. With this, it was possible to determine detection limit (DL), which resulted in 8 x 10(-9) mol L-1 for peak 1. The proposed electrode (HAP-CPE) presented good repeatability, evaluated in term of relative standard deviation (R.S.D. = 2.87%) for n = 7 and was applied for para-nitrophenol determination in water samples. The average recovery for these samples was 86.2%. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:323 / 328
页数:6
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