TY - JOUR
T1 - Electro-peroxone treatment of the antidepressant venlafaxine
T2 - Operational parameters and mechanism
AU - Li, Xiang
AU - Wang, Yujue
AU - Zhao, Jian
AU - Wang, Huijiao
AU - Wang, Bin
AU - Huang, Jun
AU - Deng, Shubo
AU - Yu, Gang
N1 - Publisher Copyright:
© 2015 Published by Elsevier B.V.
PY - 2015/12/1
Y1 - 2015/12/1
N2 - Degradation of the antidepressant venlafaxine by a novel electrocatalytic ozonation process, electro-peroxone (E-peroxone), was studied. The E-peroxone treatment involves sparging ozone generator effluent (O2 and O3 gas mixture) into an electrolysis reactor that is equipped with a carbon-polytetrafluoroethylene cathode to electrocatalytically transform O2 in the bubbled gas to H2O2. The in-situ generate H2O2 then reacts with the bubbled O3 to yield OH, which can non-selectively degrade organic compounds rapidly in the solution. Thanks to the significant OH production, the E-peroxone treatment greatly enhanced both venlafaxine degradation and total organic carbon (TOC) removal as compared to ozonation and electrolysis alone. Under optimal reaction conditions, complete venlafaxine degradation and TOC elimination could be achieved within 3 and 120min of E-peroxone process, respectively. Based on the by-products (e.g., hydroxylated venlafaxine, phenolics, and carboxylic acids) identified by UPLC-UV and UPLC/Q-TOF-mass spectrometry, plausible reaction pathways were proposed for venlafaxine mineralization by the E-peroxone process. The results of this study suggest that the E-peroxone treatment may provide a promising way to treat venlafaxine contaminated water.
AB - Degradation of the antidepressant venlafaxine by a novel electrocatalytic ozonation process, electro-peroxone (E-peroxone), was studied. The E-peroxone treatment involves sparging ozone generator effluent (O2 and O3 gas mixture) into an electrolysis reactor that is equipped with a carbon-polytetrafluoroethylene cathode to electrocatalytically transform O2 in the bubbled gas to H2O2. The in-situ generate H2O2 then reacts with the bubbled O3 to yield OH, which can non-selectively degrade organic compounds rapidly in the solution. Thanks to the significant OH production, the E-peroxone treatment greatly enhanced both venlafaxine degradation and total organic carbon (TOC) removal as compared to ozonation and electrolysis alone. Under optimal reaction conditions, complete venlafaxine degradation and TOC elimination could be achieved within 3 and 120min of E-peroxone process, respectively. Based on the by-products (e.g., hydroxylated venlafaxine, phenolics, and carboxylic acids) identified by UPLC-UV and UPLC/Q-TOF-mass spectrometry, plausible reaction pathways were proposed for venlafaxine mineralization by the E-peroxone process. The results of this study suggest that the E-peroxone treatment may provide a promising way to treat venlafaxine contaminated water.
KW - Electrocatalysis
KW - Hydrogen peroxide
KW - Hydroxyl radical
KW - Pharmaceutical
KW - Venlafaxine
UR - http://www.scopus.com/inward/record.url?scp=84937217957&partnerID=8YFLogxK
U2 - 10.1016/j.jhazmat.2015.07.004
DO - 10.1016/j.jhazmat.2015.07.004
M3 - Article
C2 - 26188873
AN - SCOPUS:84937217957
SN - 0304-3894
VL - 300
SP - 298
EP - 306
JO - Journal of Hazardous Materials
JF - Journal of Hazardous Materials
ER -