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使用掺杂铁物种的多孔碳材料修饰的玻碳电极对苯二酚和邻苯二酚的电化学测定。

Amperometric determination of hydroquinone and catechol using a glassy carbon electrode modified with a porous carbon material doped with an iron species.

机构信息

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

State Key Laboratory of Trauma, Burns and Combined Injury, Institute of Surgery Research, Daping Hospital, Third Military Medical University, Chongqing, 400042, China.

出版信息

Mikrochim Acta. 2017 Dec 7;185(1):37. doi: 10.1007/s00604-017-2538-z.

Abstract

A porous carbon material doped with an iron species (Fe/PC) was prepared by carbonizing a mixture of zeolitic imidazolate framework-8 in the presence of iron(II) ions. The resulting material was characterized by X-ray diffraction, nitrogen adsorption isotherms, transmission electron microscopy, and by Raman and X-ray photoelectron spectroscopy. Fe/PC was the deposited on the surface of glassy carbon electrode (GCE) to obtain a sensor for amperometric determination of phenolic compounds. The unique catalytic activity, good electrical conductivity and hierarchical structure of the Fe/PC composite results in good electrooxidative activity towards hydroquinone (HQ; typically at 44 mV) and catechol (CC; typically at 160 mV). Under optimal conditions, the amperometric responses are linear in the range from 0.1 to 120 μmol · L for HQ, and from 1.0 to 120 μmol · L for CC. The respective detection limits are 14 and 33 nmol · L. The sensor is highly selective against potential interferents and was successfully applied to the determination of HQ and CC contents in (spiked) water samples. Graphical abstract An amperometric sensor for phenolic compounds was constructed by using a metal-organic framework derived iron doped porous carbon material.

摘要

一种掺杂铁物种的多孔碳材料(Fe/PC)是通过在沸石咪唑酯骨架-8 的混合物存在下碳化铁(II)离子制备的。通过 X 射线衍射、氮气吸附等温线、透射电子显微镜以及拉曼和 X 射线光电子能谱对所得材料进行了表征。Fe/PC 沉积在玻碳电极(GCE)表面上,以获得用于酚类化合物安培测定的传感器。Fe/PC 复合材料独特的催化活性、良好的导电性和分层结构导致其对苯二酚(HQ;通常在 44 mV)和邻苯二酚(CC;通常在 160 mV)具有良好的电氧化活性。在最佳条件下,HQ 的安培响应在 0.1 至 120 μmol · L 的范围内呈线性,CC 的安培响应在 1.0 至 120 μmol · L 的范围内呈线性。相应的检测限分别为 14 和 33 nmol · L。该传感器对潜在干扰物具有高度选择性,并成功应用于(加标)水样中 HQ 和 CC 含量的测定。

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