Dehydroascorbic acid is shown to be converted to 2-(threo-1,2,3-trihydroxypropylkartronic acid in aqueous alkaline solutions. The structure of the acid was determined by mass spectrometry of its acyclic Me,Si derivative. Mass spectrometric and chromatographic data are compared with those of related
Development of a Method to Identify Keto Acids in Ozonated Fulvic Acid Solutions
β Scribed by Xie, Yuefeng; Reckhow, David A.
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 297 KB
- Volume
- 32
- Category
- Article
- ISSN
- 1076-5174
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β¦ Synopsis
A gas chromatographic-mass spectrometric method, combining an O-(2,3,4,5,6-pentaΓuorobenzyl)hydroxylaminediazomethane double derivatization, was developed to identify major keto acids in ozonated fulvic acid solutions. Three keto acids, glyoxylic, pyruvic, and ketomalonic acid, four aldehydes and two analytical artifacts were identi-Γed. The detailed mass spectra, obtained in both electron impact and positive chemical ionization modes, and their fragment assignments are presented. Owing to the similarity of their electron impact mass spectra, electron impact mass spectra along with positive chemical ionization mass spectra are needed to identify these keto acids reliably. The e β ects of the formation of keto acids on water quality are also discussed.
π SIMILAR VOLUMES
Asymmetrical flow field-flow fractionation AsFlFFF is used to measure the size distributions of humic acids in solution. Shifts in the size distribution are used to study the behavior of these amphiphilic macromolecules in solution with changes in pH, ionic strength, and humic acid concentration. Hu