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Evaluation of the variation in relative response factors of GC-MS analysis with the internal standard methods:
Anton Korban1, Radomír Čabala2, Vladimir Egorov3
1Faculty of Science, Department of Analytical Chemistry, Charles University, Hlavova 2030/8, 128 40, Prague 2, Czech Republic; Chemistry Faculty, Department of Analytical Chemistry, Belarusian State University, Leningradskaya 14, 220050, Minsk, Belarus; Institute for Nuclear Problems of Belarusian State University, 220006, Bobruyskaya Str., 11, Minsk, Belarus.
Abstract:
This paper focuses on the evaluation of variation of relative response factors (RRFs) obtained by two internal standard (IS) methods that are used to control the quality of alcoholic products. A standard IS method using 1-pentanol was compared with an "Ethanol as IS" method. The variation of RRF values for both methods was determined using standard solutions based on 20, 40 and 96% ethanol-water matrices. For this purpose, solutions of the ten most abundant volatile compounds were analysed at four different concentrations (250, 500, 1000 and 5000 mg L-1 absolute alcohol, AA) within these matrices. Each solution was measured four times by gas chromatography-mass spectrometry (GC-MS) in single ion monitoring (SIM) mode under repeatability conditions. Our results showed that for the 40% and 96% matrices, the ethanol and standard IS methods showed similar relative standard deviations (RSDs) variation of no more than 2% within the 250-1000 mg L-1 AA volatile compounds concentration range. For the 20% matrix as well as for the 250-5000 mg L-1 AA concentration range the resulting variation in calibration factors reaches 10% for both methods. As for the whole range of 20-96% alcohol by volume (ABV) and 250-5000 mg L-1 AA volatile concentration range, the resultant RRFs for the standard IS method (8% RSD) were more stable than those for the ethanol IS method (almost 40% RSD). Nonlinearity of the signal-to-amount dependence was also assessed with respect to the injection and detection processes.
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