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A new methodology to assess the performance of AOPs in complex samples: Application to the degradation of phenolic compounds by O 3 and O 3 /UV-A-Vis
A methodology combining experimental design methodology, liquid chromatography, excitation emission matrixes (EEM) and bioassays has been applied to study the performance of O and O /UVA-vis in the treatment of a mixture of eight phenolic pollutants. An experimental design methodology based on Doehl...
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Published in: | Chemosphere (Oxford) 2019-05, Vol.222, p.114 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Online Access: | Get full text |
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Summary: | A methodology combining experimental design methodology, liquid chromatography, excitation emission matrixes (EEM) and bioassays has been applied to study the performance of O
and O
/UVA-vis in the treatment of a mixture of eight phenolic pollutants. An experimental design methodology based on Doehlert matrixes was employed to determine the effect of pH (between 3 and 12), ozone dosage (02-1.0 g/h) and initial concentration of the pollutants (1-6 mg/L each). The following conclusions were obtained: a) acidic pH and low O
dosage resulted in an inefficient process, b) increasing pH and O
amount produced an enhancement of the reaction, and c) interaction of basic pH and high amounts of ozone decreased the efficiency of the process. The combination of O
/UVA-vis was able to enhance ozonation in those experimental regions were this reagent was less efficient, namely low pH and low ozone dosages. The application of EEM-PARAFAC showed four components, corresponding to the parent pollutants and three different groups of reaction product and its evolution with time. Bioassys indicated important detoxification (from 100% to less than 30% after 1 min of treatment with initial pollutant concentration of 6 mg/L, pH = 9 and ozone dosage of 0.8 g/h) according to the studied methods (D. magna and P. subcapitata). Also estrogenic activity and dioxin-like behavior were significantly decreased. |
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ISSN: | 1879-1298 |
DOI: | 10.1016/j.chemosphere.2019.01.015 |