A multicommuted flow system for fast screening/sequential spectrophotometric determination of dichromate, salicylic acid, hydrogen peroxide and starch in milk samples

被引:41
作者
de Souza, Gustavo Campelo S. [1 ,2 ]
Bezerra da Silva, Paulo A. [1 ,2 ]
Leoterio, Dilmo Marques da S. [1 ,2 ]
Silveira Paim, Ana Paula [2 ]
Lavorante, Andre F. [1 ]
机构
[1] Univ Fed Rural Pernambuco, Dept Ciencias Mol, BR-52171900 Recife, PE, Brazil
[2] Univ Fed Pernambuco, Dept Quim Fundamental, BR-50740560 Recife, PE, Brazil
关键词
Multicommutation; Milk; Sequential determination; Screening analysis; EXPLOITING MULTICOMMUTATION; INJECTION DETERMINATION; GREEN CHEMISTRY; WATER; MULTIDETERMINATION; QUANTIFICATION; PERFORMANCE; CONSTANT; SENSOR; MICRO;
D O I
10.1016/j.foodcont.2014.05.021
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
In this work a multicommuted flow system for the sequential screening/determination of dichromate, salicylic acid, hydrogen peroxide and starch in milk samples was developed. The concept of multicommutation in flow injection analysis was chosen, resulting in an environmentally friendly system with minimal consumption of reagents and waste generation. The proposed approach is based on a simple binary DETECT or NO-DETECT response, thereby making it possible to determine analytes quickly, with high performance and easy operation. For dichromate determination, the proposed method was based on the reaction between Cr(VI) and 1,5-diphenylcarbazide, enabling a linear working range response, between 1.0 and 10.4 mg L-1, (R = 0.999). In order to determine salicylic acid, the proposed method was based on a complexation reaction of Fe(III) and salicylic acid, with the linear working range response from 103.6 to 414.3 mg L-1 (7.5 x 10(-4)-3.0 x 10(-3) mol L-1) (R = 0.999). The hydrogen peroxide determination was based on the oxidation reaction of hydrogen peroxide with vanadium oxide (V) in an acid environment, with a linear working range of 10.0-200.0 mg L-1 (R = 0.996). Starch determination was based on the complex reaction of starch and triiodide, with a linear working range of 12.5-150.0 mg L-1 (R = 0.999). The mean sampling rate for the four species was 83 determinations per hour. Performance curves were used to verify the quantity of false positives and false negatives. Addition and recovery tests were used for validation of the proposed procedures, resulting in variation between 90.1 and 108.7% for three different samples. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:127 / 135
页数:9
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