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在存在和不存在赤藓红及喹啉黄食用色素的情况下,通过阴极溶出伏安法测定亮蓝FCF。

Determination of brilliant blue FCF in the presence and absence of erythrosine and quinoline yellow food colours by cathodic stripping voltammetry.

作者信息

Florian M, Yamanaka H, Carneiro P A, Zanoni M Valnice Boldrin

机构信息

Departamento de Química Analítica, Instituto de Química - Universidade Estadual Paulista, Caixa Postal 355, 14800-900, Araraquara - S.P., Brazil.

出版信息

Food Addit Contam. 2002 Sep;19(9):803-9. doi: 10.1080/02652030210146855.

Abstract

A study of the voltammetric behaviour of the food colours brilliant blue FCF (C.I. 42090), erythrosine (C.I. 45430) and quinoline yellow (C.I. 47005) in the pH range 2-10 have been carried out by cathodic#10; stripping voltammetry. At pH 4.5 (acetate buffer) with an accumulation potential of 0 V and accumulation time of 30s, the voltammograms presented well-defined reduction peaks at potential - 0.76 V for brilliant blue FCF, - 0.85 V for quinoline yellow and - 0.54 V for erythrosine. Linear calibration graphs were obtained from 8 to 80 microg l(-1) brilliant blue, from 4 to 43 microg l(-1) quinoline yellow and from 10 to 70 microg l(-1) erythrosine. The method has been successfully applied to identify and quantify binary mixtures of these dyes and applied for determining brilliant blue FCF in commercial food products.

摘要

采用阴极溶出伏安法研究了食用色素亮蓝FCF(C.I. 42090)、赤藓红(C.I. 45430)和喹啉黄(C.I. 47005)在pH值为2至10范围内的伏安行为。在pH 4.5(醋酸盐缓冲液)、富集电位为0 V、富集时间为30 s的条件下,伏安图显示亮蓝FCF在电位-0.76 V处有清晰的还原峰,喹啉黄在-0.85 V处,赤藓红在-0.54 V处。亮蓝在8至80 μg l⁻¹、喹啉黄在4至43 μg l⁻¹、赤藓红在10至70 μg l⁻¹范围内获得了线性校准曲线。该方法已成功应用于鉴定和定量这些染料的二元混合物,并用于测定商业食品中的亮蓝FCF。

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