VUV-photolysis of aqueous solutions of hydroxylamine and nitric oxide. Effect of organic matter: phenol
VUV-irradiation of aqueous solutions containing hydroxylamine (NH 2 OH) in its acid form (NH 3 OH + ) and phenol (C 6 H 5 OH) results in the simultaneous mineralization of the organic substrate and the almost quantitative reduction of NH 3 OH + to ammonium ions (NH 4 + ). Irradiation of aqueous solu...
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Veröffentlicht in: | Photochemical & photobiological sciences 2019-09, Vol.18 (9), p.224-2247 |
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Sprache: | eng |
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Zusammenfassung: | VUV-irradiation of aqueous solutions containing hydroxylamine (NH
2
OH) in its acid form (NH
3
OH
+
) and phenol (C
6
H
5
OH) results in the simultaneous mineralization of the organic substrate and the almost quantitative reduction of NH
3
OH
+
to ammonium ions (NH
4
+
). Irradiation of aqueous solutions of NH
3
OH
+
in the absence of organic substrates showed the formation of nitrate (NO
3
−
) and nitrite (NO
2
−
) and minor quantities of NH
4
+
. In line with these experiments, VUV-irradiation of aqueous solutions of nitrogen monoxide (NO&z.rad;) yields NH
4
+
only when C
6
H
5
OH is simultaneously mineralized. A possible reaction mechanism is discussed, where reactions of NO&z.rad; and NH
3
OH
+
with hydrogen atoms (H&z.rad;), hydroxyl radicals (HO&z.rad;) and hydrated electrons (e
−
aq
), all generated by the VUV-photochemically initiated homolysis of water, are of great importance to the observed results. In the presence of phenol, competition between phenol and either NO&z.rad; or NH
3
OH
+
for these reactive intermediates in the primary volume of reactions strongly determines the oxidation state and nature of the N-containing products. C-Centered radicals and intermediate products of reactions may also have an important effect on the overall mechanism. The present results are discussed in relation to the actual state of knowledge presented in the literature.
VUV-irradiation of aqueous solutions containing, both, hydroxylamine (NH
2
OH/NH
3
OH
+
) and phenol results in the mineralization of the organic substrate and the quantitative reduction of NH
3
OH
+
to NH
4
+
ions. |
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ISSN: | 1474-905X 1474-9092 |
DOI: | 10.1039/c9pp00143c |