Laboratoire de Chimie Analytique, Département de Chimie Inorganique, Faculté des Sciences, Université de Yaoundé I, Yaoundé, Cameroun. herveleclerc@yahoo
Talanta. 2010 May 15;81(3):972-9. doi: 10.1016/j.talanta.2010.01.049. Epub 2010 Feb 1.
In this study, an hybrid material obtained by the intercalation of a gemini surfactant between the layers of smectite-type clay, was fully characterized by X-ray diffraction (XRD), infrared spectroscopy (FTIR) and N(2) adsorption-desorption experiments (BET method). To ascertain the intercalation process of the starting clay by the dimeric surfactant, the permselectivity and ion exchange properties of the organoclay were investigated by ion exchange voltammetry using Fe(CN)(6) and Ru(NH(3))(6) as redox probes, by the means of a clay film-modified electrode. Due to its organophilic character, the surfactant-intercalated complex was evaluated as electrode modifier for the accumulation of methylparathion (MP) pesticide. The electroanalytical procedure involves two steps: preconcentration under open-circuit followed by voltammetric detection by square wave voltammetry: the peak current obtained (after 5min preconcentration in 4x10(-5)molL(-1)MP) on a glassy carbon electrode coated by a thin film of the modified clay was more than five times higher than that exhibited by the same substrate covered by a film of the pristine clay. This opens the way to the development of a sensitive method for the detection of the pesticide. Many parameters that can affect the stripping response (surfactant loading of the hybrid material, film composition, pH of the detection medium, preconcentration time, electrolysis potential and duration as well as some other instrumental parameters) were systematically investigated to optimize the sensitivity of the organoclay-modified electrode. After optimization, a linear calibration curve for MP was obtained in the concentration range from 4x10(-7) to 8.5x10(-6)molL(-1) in acetate buffer (pH 5), with a detection limit of 7x10(-8)molL(-1) (signal-to-noise ratio equal to 3). The interference effect of various inorganic ions likely to influence the stripping determination of the pesticide was also examined, and the described method was applied to spring water analysis.
在这项研究中,通过将双子表面活性剂插入到层状蒙脱石粘土之间,得到了一种杂化材料,并通过 X 射线衍射(XRD)、红外光谱(FTIR)和 N2 吸附-解吸实验(BET 法)对其进行了全面表征。为了确定起始粘土被二聚表面活性剂插层的过程,通过使用 [Fe(CN)(6)]3-和 [Ru(NH3)6]3+作为氧化还原探针的离子交换伏安法,以及通过粘土膜修饰电极,研究了有机粘土的选择透过性和离子交换性能。由于其亲油性,该表面活性剂插层复合物被评估为用于积累甲基对硫磷(MP)农药的电极修饰剂。电分析程序包括两个步骤:开路下的预浓缩,然后通过方波伏安法进行伏安检测:在玻璃碳电极上涂覆一层由改性粘土制成的薄膜,在 4x10(-5)molL(-1)MP 中进行 5 分钟预浓缩后,获得的峰电流(与涂覆原始粘土薄膜的相同基底相比)高于五倍。这为开发一种用于检测农药的灵敏方法开辟了道路。许多可以影响剥离响应的参数(杂化材料的表面活性剂负载量、薄膜组成、检测介质的 pH 值、预浓缩时间、电解电位和持续时间以及其他一些仪器参数)都进行了系统研究,以优化有机粘土修饰电极的灵敏度。优化后,在醋酸盐缓冲液(pH 5)中,从 4x10(-7)到 8.5x10(-6)molL(-1)的范围内,获得了 MP 的线性校准曲线,检测限为 7x10(-8)molL(-1)(信噪比等于 3)。还检查了各种可能影响农药剥离测定的无机离子的干扰效应,并将所述方法应用于泉水分析。