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采用壳聚糖功能化银纳米粒子修饰的多壁碳纳米管糊电极伏安法测定亚硝酸盐。

Voltammetric determination of nitrite by using a multiwalled carbon nanotube paste electrode modified with chitosan-functionalized silver nanoparticles.

机构信息

Department of Chemistry, University of Science & technology, KPK, Bannu, 28100, Pakistan.

Interdisciplinary Research Centre in Biomedical Materials (IRCBM), COMSATS University Islamabad, Campus, Lahore, 54000, Pakistan.

出版信息

Mikrochim Acta. 2019 Aug 2;186(9):595. doi: 10.1007/s00604-019-3699-8.

Abstract

A cyclic voltammetric method is described for the determination of nitrite by using a multiwalled carbon nanotube paste electrode (MWCNT) that was modified with chitosan-functionalized silver nanoparticles (Chit-AgNPs). The AgNPs were prepared by one step procedure using chitosan as stabilizing agent. The resulting modified AgNPs were drop-coated onto the electrode. By combining the advantages of chitosan, AgNPs (in the form of Chit-AgNPs) and MWCNT, the assay exhibits a remarkable improvement in the cyclic voltammetric response towards the oxidation of nitrite at a typical peak potential of 0.81 V (vs. SCE) in buffer of pH 4.0. The accumulation of nitrite on the electrode also was achieved, and this further enhances the analytical sensitivity. Under optimized conditions, the oxidation peak current increases linearly in the 100 nM to 50 μM nitrite concentration range, and the detection limit is 30 nM. The method has high selectivity for nitrite even in the presence of other potentially interfering ions. Graphical abstract Schematic illustration of the prepared chitosan functionalized silver nanoparticles (transmission electron microscope image) and modification of multi-walled carbon nanotube paste electrode with chitosan functionalized silver nanoparticles for the electrochemical oxidation of nitrite to nitrate.

摘要

一种循环伏安法用于测定亚硝酸盐,使用壳聚糖功能化的银纳米粒子(Chit-AgNPs)修饰的多壁碳纳米管糊电极(MWCNT)。AgNPs 通过一步法制备,壳聚糖作为稳定剂。所得修饰的 AgNPs 被滴涂在电极上。通过结合壳聚糖、AgNPs(以 Chit-AgNPs 的形式)和 MWCNT 的优点,该测定法在 pH 4.0 的缓冲液中对亚硝酸盐的氧化表现出显著改善的循环伏安响应,典型的峰电位为 0.81 V(相对于 SCE)。还可以在电极上进行亚硝酸盐的积累,这进一步提高了分析灵敏度。在优化条件下,氧化峰电流在 100 nM 至 50 μM 亚硝酸盐浓度范围内呈线性增加,检测限为 30 nM。该方法对亚硝酸盐具有高选择性,即使存在其他潜在干扰离子也是如此。

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