首页> 美国卫生研究院文献>Journal of Analytical Methods in Chemistry >Dioctylsulfosuccinate Functionalized NiAl-Layered Double Hydroxide for Sensitive Fenuron Electroanalysis Using a Carbon Paste Electrode
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Dioctylsulfosuccinate Functionalized NiAl-Layered Double Hydroxide for Sensitive Fenuron Electroanalysis Using a Carbon Paste Electrode

机译:二辛基磺基琥珀酸酯官能化 NiAl-层状双氢氧化物用于使用碳膏电极进行灵敏的 Fenuron 电分析

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摘要

Environmental pollution resulting from the use of pesticides such as fenuron poses significant health risks due to the carcinogenic and teratogenic properties of these compounds. There is an urgent need to develop rapid and cost-effective detection methods for quantifying fenuron. In this study, an inorganic-organic composite material was obtained by intercalating sodium dioctylsulfosuccinate (DSS) within the interlayer space of a nickel-aluminum-layered double hydroxide (NiAl-LDH). The pristine and modified LDHs (NiAl-LDH) were characterized using Fourier transform infrared, X-ray diffraction, and thermogravimetric analysis, confirming the successful intercalation of DSS in the mineral structure. The modified LDH was used to elaborate a sensor for detecting fenuron herbicide via differential pulse voltammetry (DPV) employing a carbon paste electrode (CPE). The electrochemical procedure for fenuron analysis consisted of immersing the working electrode in an electrolytic solution containing the appropriate amount of fenuron, followed by voltammetry detection without any preconcentration step. Compared to CPE modified by pristine LDH, the peak current obtained on the organo-LDH-modified CPE was twice as high. The increase in the fenuron signal was attributed to the high organophilic feature of this composite material induced by DSS modification. To optimize the sensitivity of the organo-LDH modified electrode, the effects of several experimental parameters such as pH of the medium and proportion of the modifier in the paste on the stripping response were examined. Linear calibration curves were obtained for the fenuron concentrations ranging from 0.5 × 10−6 to 1 × 10−6 mol.L−1 and 1 × 10−6 to 5 × 10−6 mol.L−1. The limit of detection (LOD) calculated on the basis of a signal-to-noise ratio of 3 was found to be 1.8 × 10−8 mol.L−1 for the low concentration range with a limit of quantification (LOQ) which was 6 × 10−8 mol.L−1. Furthermore, the interference effect of several inorganic ions and other pesticides potentially affecting fenuron stripping was explored, and the method's applicability was confirmed by determining fenuron levels in a river sample taken from down-town Yaoundé.
机译:由于这些化合物的致癌和致畸特性,使用葫芦脲等杀虫剂造成的环境污染会带来重大的健康风险。迫切需要开发快速且具有成本效益的检测方法来定量 fenuron。在本研究中,通过在镍铝层状双氢氧化物 (NiAl-LDH) 的层间空间内嵌入二辛基磺基琥珀酸钠 (DSS) 获得了无机-有机复合材料。使用傅里叶变换红外、X 射线衍射和热重分析对原始和改性 LDH (NiAl-LDH) 进行了表征,证实了 DSS 在矿物结构中的成功嵌入。改性的 LDH 用于制作一种传感器,用于通过采用碳膏电极 (CPE) 的差分脉冲伏安法 (DPV) 检测氟脲除草剂。葫草脲分析的电化学程序包括将工作电极浸入含有适量腥脲的电解液中,然后进行伏安法检测,无需任何预浓缩步骤。与由原始 LDH 修饰的 CPE 相比,有机 LDH 修饰的 CPE 上获得的峰值电流高出两倍。葫芦脲信号的增加归因于 DSS 修饰诱导的这种复合材料的高亲有机特性。为了优化有机 LDH 修饰电极的灵敏度,检查了几个实验参数(如培养基的 pH 值和浆料中改性剂的比例)对剥离响应的影响。获得 0.5 × 10-6 至 10-6 mol × 10-6 mol 的葫草隆浓度的线性校准曲线。L-1 和 1 × 10-6 至 5 × 10-6 mol。L−1.根据信噪比 3 计算的检测限 (LOD) 为 1.8 × 10−8 mol。L−1 用于低浓度范围,定量限 (LOQ) 为 6 × 10−8 mol。L−1.此外,还探讨了几种可能影响葫脲剥离的无机离子和其他农药的干扰作用,并通过测定从雅温得市中心采集的河流样本中的葫草脲水平来证实该方法的适用性。

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