Potential of pulsed corona discharges generated in water for the degradation of persistent pharmaceutical residues
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
26218466
DOI
10.1016/j.watres.2015.07.018
PII: S0043-1354(15)30120-2
Knihovny.cz E-zdroje
- Klíčová slova
- Advanced oxidation, Diclofenac, Ethinylestradiol, Hydroxyl radicals, Non-thermal plasma, Phenol,
- MeSH
- chemické látky znečišťující vodu chemie MeSH
- čištění vody metody MeSH
- diatrizoát chemie MeSH
- diazepam chemie MeSH
- diklofenak chemie MeSH
- ethinylestradiol chemie MeSH
- ibuprofen chemie MeSH
- karbamazepin chemie MeSH
- monitorování životního prostředí MeSH
- odpad tekutý - odstraňování metody MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- chemické látky znečišťující vodu MeSH
- diatrizoát MeSH
- diazepam MeSH
- diklofenak MeSH
- ethinylestradiol MeSH
- ibuprofen MeSH
- karbamazepin MeSH
Anthropogenic pollutants and in particular pharmaceutical residues are a potential risk for potable water where they are found in increasing concentrations. Different environmental effects could already be linked to the presence of pharmaceuticals in surface waters even for low concentrations. Many pharmaceuticals withstand conventional water treatment technologies. Consequently, there is a need for new water purification techniques. Advanced oxidation processes (AOP), and especially plasmas with their ability to create reactive species directly in water, may offer a promising solution. We developed a plasma reactor with a coaxial geometry to generate large volume corona discharges directly in water and investigated the degradation of seven recalcitrant pharmaceuticals (carbamazepine, diatrizoate, diazepam, diclofenac, ibuprofen, 17α-ethinylestradiol, trimethoprim). For most substances we observed decomposition rates from 45% to 99% for treatment times of 15-66 min. Especially ethinylestradiol and diclofenac were readily decomposed. As an inherent advantage of the method, we found no acidification and only an insignificant increase in nitrate/nitrite concentrations below legal limits for the treatment. Studies on the basic plasma chemical processes for the model system of phenol showed that the degradation is primarily caused by hydroxyl radicals.
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