“…There are some works on the direct GC determination of short chain carboxylic acids without their derivatization [5,20]. Zenkevich et al [20] suggest that derivatization is desirable or necessary for simple dicarboxylic acids but could be omitted for monocarboxylic acids.…”
Section: Gas Chromatographic Determination Of Carboxylic Acidsmentioning
confidence: 99%
“…There are some works on the direct GC determination of short chain carboxylic acids without their derivatization [5,20]. Zenkevich et al [20] suggest that derivatization is desirable or necessary for simple dicarboxylic acids but could be omitted for monocarboxylic acids. Thus, to verify the possibility of gas chromatographic determination of the analytes of interest (acetic acid, propionic acid, oxalic acid and succinic acid) without their derivatization, the solutions of the acids in acetone were directly injected into the GC system.…”
Section: Gas Chromatographic Determination Of Carboxylic Acidsmentioning
Headspace gas chromatographic analysis is suggested for the determination of acetic and propionic acids in aqueous media. Derivatization of the acids was accomplished by tributyl borate. The derivatization and headspace extraction were coupled into a single step. Analytical characteristics of the suggested technique at the optimized derivatization/headspace extraction conditions were determined. The technique was applied for the analysis of bakery products, ketchup, tomato paste and kefir.
“…There are some works on the direct GC determination of short chain carboxylic acids without their derivatization [5,20]. Zenkevich et al [20] suggest that derivatization is desirable or necessary for simple dicarboxylic acids but could be omitted for monocarboxylic acids.…”
Section: Gas Chromatographic Determination Of Carboxylic Acidsmentioning
confidence: 99%
“…There are some works on the direct GC determination of short chain carboxylic acids without their derivatization [5,20]. Zenkevich et al [20] suggest that derivatization is desirable or necessary for simple dicarboxylic acids but could be omitted for monocarboxylic acids. Thus, to verify the possibility of gas chromatographic determination of the analytes of interest (acetic acid, propionic acid, oxalic acid and succinic acid) without their derivatization, the solutions of the acids in acetone were directly injected into the GC system.…”
Section: Gas Chromatographic Determination Of Carboxylic Acidsmentioning
Headspace gas chromatographic analysis is suggested for the determination of acetic and propionic acids in aqueous media. Derivatization of the acids was accomplished by tributyl borate. The derivatization and headspace extraction were coupled into a single step. Analytical characteristics of the suggested technique at the optimized derivatization/headspace extraction conditions were determined. The technique was applied for the analysis of bakery products, ketchup, tomato paste and kefir.
Аналитика и контроль. 2020. Т. 24. № 2.GC systems. In addition to that, the simplification of experimental opera tions and minimizing the number of parallel determina ti ons as well as more rational algorithm of data processing was achieved. The essence of the modified appro ach was the approximation of S rel = f(pm) data sets with the 3 rd degree polynomials, following by comparing these data with the averaged S rel (with standard deviations) values for the most reproducible S rel values of three test-so lu tions with the highest concentrations of test-compounds. It was shown that the limits of the inertness for the WCOT-column (with the standard non-polar polydimethylsiloxane stationary phase) were from the fractions of nano gram to several nanograms of polar analytes in the chromatographic zone. The results for the test-samples contained some polar constituents (e.g., benzyl alco hol) which lead to suggesting that the integral manifestations of the insufficient inertness could be caused not only by the influence of chromatographic systems, but also by the sorp tion of polar analytes on the surfaces of vials used for the dilution of test-samples. The differences in m lim values for the same polar components at the same analytical conditions, when the dilutions were carried out in the glass or polypropylene vials, were revealed.
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