Remote Instrumentation Lab, University Science Instrumentation Centre, Dayalbagh Educational Institute, Agra 282110 UP, India.
Environ Sci Pollut Res Int. 2013 May;20(5):3068-76. doi: 10.1007/s11356-012-1194-4. Epub 2012 Oct 4.
In recent years, increasing awareness of the environmental impact of heavy metals has prompted a demand for monitoring and decontaminating industrial wastes prior to discharging into natural water bodies. This paper describes the preparation and electrochemical application of carbon paste electrode modified with nanocellulosic fibers for the determination of cadmium and lead in water samples using anodic stripping voltammetry. First, cadmium and lead were adsorbed on the carbon paste electrode surface at open circuit potential, followed by anodic stripping voltammetric scan from -1 to 0 V. Different factors affecting sensitivity and precision of the electrode, including accumulating solvent, pH of the accumulating solvent, accumulation time, supporting electrolyte, and scan rate were investigated. The proposed method was also applied to the determination of Cd (II) and Pb (II) in the presence of other interfering metal ions and cetyl trimethyl ammonium bromide, sodium dodecyl sulfate, and Triton X-100 as a representative of cationic, anionic, and neutral surfactants. Linear calibration curves were obtained in the concentration ranges of 150-650 μg L(-1) and 80-300 μg L(-1), respectively, for cadmium and lead at an accumulated time of 10 min with limits of detection 88 and 33 μg L(-1). Optimized working conditions are defined as acetate buffer of pH 5 as accumulating solvent, hydrochloric acid as supporting electrolyte, and scan rate 50 mV/s. This technique does not use mercury and therefore has a positive environmental benefit. The method is reasonably sensitive and selective and has been successfully applied to the determination of trace amounts of Cd (II) and Pb (II) in water samples.
近年来,人们对重金属对环境的影响的认识不断提高,促使人们要求在将工业废物排放到自然水体之前对其进行监测和净化。本文描述了纳米纤维素纤维修饰的碳糊电极的制备及其在阳极溶出伏安法中的电化学应用,用于水样中镉和铅的测定。首先,在开路电位下,镉和铅被吸附在碳糊电极表面上,然后进行从-1 到 0 V 的阳极溶出伏安扫描。研究了影响电极灵敏度和精度的不同因素,包括累积溶剂、累积溶剂的 pH 值、累积时间、支持电解质和扫描速率。该方法还用于在存在其他干扰金属离子和十六烷基三甲基溴化铵、十二烷基硫酸钠和 Triton X-100 的情况下测定 Cd(II)和 Pb(II),后三者分别代表阳离子、阴离子和中性表面活性剂。在 10 分钟的累积时间下,镉和铅的浓度范围分别为 150-650 μg L(-1)和 80-300 μg L(-1),得到了线性校准曲线,检测限分别为 88 和 33 μg L(-1)。优化的工作条件定义为 pH 5 的乙酸盐缓冲液作为累积溶剂、盐酸作为支持电解质和 50 mV/s 的扫描速率。该技术不使用汞,因此具有积极的环境效益。该方法具有合理的灵敏度和选择性,已成功应用于水样中痕量 Cd(II)和 Pb(II)的测定。