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在裸掺硼金刚石电极上伏安法测定饮料样品中的咖啡因。

Voltammetric determination of caffeine in beverage samples on bare boron-doped diamond electrode.

机构信息

Institute of Analytical Chemistry, Faculty of Chemical and Food Technology, Slovak University of Technology, Radlinského 9, Bratislava SK-812 37, Slovak Republic.

出版信息

Food Chem. 2012 Dec 1;135(3):1198-204. doi: 10.1016/j.foodchem.2012.05.052. Epub 2012 May 18.

Abstract

A sensitive and selective electrochemical method for the caffeine determination using bare boron-doped diamond electrode was developed. It was found that caffeine provided highly reproducible and well-defined irreversible oxidation peak at very positive potential. The effects of supporting electrolyte, pH and scan rate on the voltammetric response of caffeine oxidation were studied to select the optimum experimental conditions. Linear response of peak current on the concentration in the range from 4×10(-7) to 2.5×10(-5)M, good repeatability (RSD of 2.1%) and detection limit of 1.5×10(-7)M without any chemical modifications and electrochemical surface pretreatment were evaluated. The effect of possible interferents appeared to be negligible which evidently proved very good selectivity. The proposed method was successfully applied for the caffeine determination in commercially available beverage samples, with results in a close statistical agreement to those declared by manufacturer and HPLC used as independent method.

摘要

本文采用裸硼掺杂金刚石电极发展了一种灵敏且选择性的电化学方法用于咖啡因的测定。结果发现,咖啡因在非常正的电势下提供了高度重现且定义良好的不可逆氧化峰。研究了支持电解质、pH 值和扫描速率对咖啡因氧化伏安响应的影响,以选择最佳的实验条件。在未进行任何化学修饰和电化学表面预处理的情况下,在 4×10(-7) 到 2.5×10(-5) M 的浓度范围内,峰电流与浓度呈线性响应,重复性好(RSD 为 2.1%),检测限为 1.5×10(-7) M。可能存在的干扰物质的影响可忽略不计,这明显证明了该方法具有很好的选择性。该方法成功地应用于市售饮料样品中咖啡因的测定,结果与制造商声明值和作为独立方法的 HPLC 非常吻合。

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