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多壁碳纳米管和金属有机骨架纳米复合材料作为新型混合电极材料,用于阀上实验室中纳摩尔级别的铅的测定。

Multi-walled carbon nanotubes and metal-organic framework nanocomposites as novel hybrid electrode materials for the determination of nano-molar levels of lead in a lab-on-valve format.

机构信息

College of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, China.

出版信息

Analyst. 2013 Sep 7;138(17):5113-20. doi: 10.1039/c3an00598d. Epub 2013 Jul 12.

DOI:10.1039/c3an00598d
PMID:23853779
Abstract

Metal-organic frameworks have been the subject of intense research because of their unique physicochemical properties. The presented study investigates the application of multi-wall carbon nanotubes and metal-organic frameworks (MWCNTs@Cu3(BTC)2) nanoparticles-modified electrode for the determination of trace levels of lead. The nanocomposites were prepared by solvothermal synthesis and characterized in detail. The experimental procedure was carried out by accumulating lead on the electrode surface and subsequently measuring with differential pulse anodic stripping voltammetry in a lab-on-valve format. The main parameters affecting the analytical performance, including the amount of MWCNTs@Cu3(BTC)2 suspension, supporting electrolyte and its pH, stripping mode, and flow rate, have been investigated in detail. Under the optimum conditions, the oxidation peak current displayed a calibration response for lead over a concentration range from 1.0 × 10(-9) to 5.0 × 10(-8) mol L(-1) with a excellent detection limit of 7.9 × 10(-10) mol L(-1). The relative standard deviation of 7 successive scans was 3.10% for 1.0 × 10(-8) mol L(-1) lead. The established method showed a great improvement in sensitivity and sample throughput for lead analysis.

摘要

金属有机骨架因其独特的物理化学性质而成为研究热点。本研究探讨了多壁碳纳米管和金属有机骨架(MWCNTs@Cu3(BTC)2)纳米粒子修饰电极在痕量铅测定中的应用。通过溶剂热合成制备了纳米复合材料,并对其进行了详细的表征。实验过程通过在电极表面上积累铅,随后以阀上实验室格式进行差分脉冲阳极溶出伏安法进行测量。详细研究了影响分析性能的主要参数,包括 MWCNTs@Cu3(BTC)2悬浮液的量、支持电解质及其 pH 值、剥离模式和流速。在最佳条件下,氧化峰电流在 1.0×10(-9)至 5.0×10(-8)mol L(-1)浓度范围内对铅显示出校准响应,检测限低至 7.9×10(-10)mol L(-1)。对于 1.0×10(-8)mol L(-1)的铅,7 次连续扫描的相对标准偏差为 3.10%。所建立的方法在灵敏度和样品通量方面对铅分析有了很大的改进。

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