Voltammetric determination of trace amounts of diacetyl at a mercury meniscus modified silver solid amalgam electrode following gas-diffusion microextraction

被引:15
|
作者
Ramos, Rui M. [1 ]
Goncalves, Luis M. [1 ]
Vyskocil, Vlastimil [2 ]
Rodrigues, Jose A. [1 ]
机构
[1] Univ Porto, REQUIMTE LAQV, Dept Quim & Bioquim, Fac Ciencias, Rua Campo Alegre 687, P-4169007 Oporto, Portugal
[2] Charles Univ Prague, Dept Analyt Chem, Fac Sci, UNESCO Lab Environm Electrochem, Hlavova 2030-8, Prague 12843 2, Czech Republic
关键词
Food analysis; Food control; Electroanalysis; Sample preparation; Differential pulse voltammetry (DPV); Volatile extraction; ALPHA-DICARBONYL COMPOUNDS; PRINTED CARBON ELECTRODES; ACCURATE GC/MS METHOD; CHROMATOGRAPHIC ANALYSIS; VICINAL DIKETONES; HPLC-UV; QUINOXALINE DERIVATIVES; PHASE MICROEXTRACTION; QUANTITATIVE-ANALYSIS; EXTRACTED COMPOUNDS;
D O I
10.1016/j.talanta.2017.03.077
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A new approach was developed for the determination of trace amounts of diacetyl in food products using gas diffusion microextraction (GDME) and subsequent detection by differential pulse voltammetry (DPV) at a mercury meniscus modified silver solid amalgam electrode (m-AgSAE). Diacetyl is a vicinal diketone responsible for the buttery aroma in many fermented foods and beverages. Its determination is important not only for evaluation of the final product quality (note of mention: health related concerns were associated with continuous diacetyl exposure) but also to monitor fermentation. GDME, a technique combining gas diffusion and microextraction, particularly aimed to volatile and semi-volatile analytes, seemed the best way to selective extract diacetyl. A solution of 0.05% o-phenylenediamine (OPDA) prepared in a Britton-Robinson buffer (pH 5.0) was chosen as the extracting solution. This solution simultaneously extracts, pre-concentrates and derivatizes diacetyl to 2,3-dimethylquinoxaline (DMQ), enhancing the extraction selectivity and making the analyte electroactive. After finding the optimum conditions for the extraction process (10 min at 60 degrees C with 1.0 mL of OPDA at pH 5.0), the DPV measurements at the m-AgSAE were conducted with a scan rate of 7 mV s(-1), a modulation amplitude of 50 mV and a modulation time of 100 ms. Under these conditions, the resulting DMQ could be easily measured at a potential of -0.6 V vs. Ag vertical bar AgCl (3 mol L-1 KCl). The amalgam electrode keeps the advantages of classic mercury electrodes, like high sensitivity, while being environmentally friendly. The GDME/m-AgSAE produced suitable method features for the determination of low amounts of diacetyl (as DMQ) in alcoholic beverages, and in fact, to the best of our knowledge, the limit of quantification of 0.18 mu g L-1 is one of the lowest reported in literature.
引用
收藏
页码:203 / 208
页数:6
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