4.7 Article

Degradation of anti-inflammatory drug dexamethasone by pulsed corona discharge: The effect of peroxycompounds addition

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.jece.2022.108042

关键词

Dexamethasone; Non-thermal plasma; Energy efficiency; Persulfate; Hydrogen peroxide; Groundwater

资金

  1. Institutional Development Program of Tallinn University of Technology [2014-2020.4.01.16-0032]
  2. EU Regional Development Fund
  3. City Council Scholarship - City of Tallinn

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The oxidation of anti-inflammatory dexamethasone in water using gas-phase pulsed corona discharge (PCD) with the addition of extrinsic oxidants was experimentally studied. The results showed that the degradation of dexamethasone was faster and more efficient in acidic media, and the combination of PCD and peroxydisulfate showed the highest removal efficiency. In groundwater matrix, the PCD/peroxydisulfate and PCD/hydrogen peroxide combinations demonstrated considerably faster degradation and mineralization of dexamethasone at higher efficiency.
The oxidation of anti-inflammatory dexamethasone (DXM) in water was experimentally studied using a gasphase pulsed corona discharge (PCD) with the addition of extrinsic oxidants: peroxydisulfate (PDS), peroxymonosulfate (PMS), and hydrogen peroxide (H2O2), aiming the increased energy and overall treatment efficiency. The effects of pH, the dose of supplementary oxidant, and the composition of real water matrix on the efficiency of DXM oxidation were established. For PCD and the PCD/oxidant combinations, a faster and more complete degradation of DXM was observed in acidic media. In neutral media, the PCD/PDS process showed the highest TOC removal and energy efficiency of DXM oxidation. Overall, the carefully optimized dose of extrinsic oxidant resulted in a perceptible improvement of oxidation efficiency in PCD/PDS and PCD/H2O2 combinations compared to PCD under similar treatment conditions. In the groundwater matrix, the use of PCD/PDS and PCD/ H2O2 combinations demonstrated considerably faster DXM degradation and mineralization at higher efficiency. The results of this study contribute to the possible application of combined PCD/oxidant processes for efficient removal of DXM from polluted water matrices.

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