Abstract
The oxidative degradation of 3-amino 5-methyl isoxazole initiated by the VUV photolysis of water at 172 nm has been studied. Mineralization of CO2, H2O, NO −3 and NH +4 is more efficient when reductive conditions (argon saturated solutions) are favoured. Formation of compounds which cannot be completely oxidised to CO2 is observed. Experiments performed under strictly oxidative conditions show higher yields of these inert compounds and, hence, incomplete mineralization. Cyanide was formed in concentrations lower than 5×10−5 mol/l. In alkaline aqueous solutions, cyanide is completely transformed into CO 2−3 , NH +4 and NO −3 during the irradiation time needed to mineralize the isoxazole. Therefore, cyanide does not present a potential risk for the use of the VUV photolysis for isoxazole degradation. Similarly, organic nitrogen is converted into both, NO −3 and NH +4 . The relative concentrations of the two ions depend on total irradiation time, oxygen saturation and reactor geometry. A sequence of reactions is proposed and discussed.
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Dedicated to Professor Dr. Dieter Klockow on the occasion of his 60th birthday
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Gonzalez, M.C., Hashem, T.M., Jakob, L. et al. Oxidative degradation of nitrogen-containing organic compounds: vaccum-ultraviolet (VUV) photolysis of aqueous solutions of 3-amino 5-methylisoxazole. Fresenius J Anal Chem 351, 92–97 (1995). https://doi.org/10.1007/BF00324297
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DOI: https://doi.org/10.1007/BF00324297