FIELD: food industry.
SUBSTANCE: sample is distilled at the temperature of 50, 78 and 90°C. Aliquots of distilled fractions of distillate are placed into ampoules, where oxidised copper oxide is previously placed, frozen, ampoules are vacuumised and sealed. Aliquot of each fraction is burnt to produce carbon dioxide, which is quantitatively collected and exposed to isotopic mass spectrometric analysis. In process of analysis, currents provided by quantity of ions with m/z 44(12C16O2 +), m/z 45(13C16O2 +) and m/z 46(12C16O18O) are alternately registered in mass spectra of carbon dioxide sample and laboratory standard. Characteristics of isotopic composition of carbon dioxide produced when each fraction of distillate is burnt, relative to international carbon standard V-PDB, are defined in relative units δ16C (‰), using formula, included into software for mass-spectrometer Delta V plus Thermo Finnigan, of the following type: δ13C=(Rs/Rst-1)·1000(‰), where Rs=([13C16O2]/[12C16O2])s, Rst=([13C16O2]/[12C16O2])st, Rs and Rst - ratios of abundances of stable isotopes 13C and 12C in analysed carbon dioxide, produced when fraction of distillate and standard are burnt. Isotopic characteristics of carbon composition are defined in reference samples produced using available samples of ethanol. Produced ratios of abundances of stable isotopes 13C and 12C are compared to each other and to characteristics of reference sample, and extent of match or deviation is used to justify origin of ethanol. Difference in values of quantitative isotopic characteristics of carbon in all fractions of distillate that exceeds 0.5‰ is used to detect availability of ethanol of non-grape origin in sample.
EFFECT: increased accuracy and validity of method.
2 tbl, 6 ex
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SU1456887A1 |
Authors
Dates
2010-10-10—Published
2009-09-22—Filed