Activating peroxymonosulfate by halogenated and methylated quinones: performance and mechanism. Issue 47 (30th August 2019)
- Record Type:
- Journal Article
- Title:
- Activating peroxymonosulfate by halogenated and methylated quinones: performance and mechanism. Issue 47 (30th August 2019)
- Main Title:
- Activating peroxymonosulfate by halogenated and methylated quinones: performance and mechanism
- Authors:
- Zhang, Hong
Qiao, Lina
He, Jing
Li, Na
Zhang, Dongmei
Yu, Kai
You, Hong
Jiang, Jie - Abstract:
- Abstract : This work describes the efficiency and mechanism of peroxymonosulfate (PMS) activation by benzoquinone with different functional groups for sulfamethoxazole degradation. Abstract : Activation of peroxymonosulfate (PMS) by halogenated and methylated quinones for destroying sulfamethoxazole (SMX) was investigated, where 2, 6-dimethyl-1, 4-benzoquinone (DMBQ), 2, 6-dichloro-1, 4-benzoquinone (DCBQ), and tetrafluoro-1, 4-benzoquinone (TFBQ) were chosen as model quinones. The PMS could be activated by halogenated and methylated quinones efficiently for SMX degradation, and the process showed high pH and quinones dependency. Different from PMS activated by ultraviolet (UV), singlet oxygen ( 1 O2 ) instead of hydroxyl radical (˙OH) and sulfate radical (SO4 ˙ − ) was the primary oxidizing species in the activation process. The formation of 1 O2 was confirmed by various quenching studies combined with chemical probes (9, 10-diphenylanthracene (DPA)). By sampling in situ and monitoring in real time, droplet spray ionization mass spectrometry (DSI-MS) was applied to capture and identify the intermediates generated in the activation process. A possible mechanism for PMS activation was proposed accordingly. It was found that a series of reactions between PMS and halogenated/methylated quinones formed a dioxirane intermediate, and the subsequent decomposition of this intermediate produced the 1 O2 . These findings would help to better understand the interactions between PMS andAbstract : This work describes the efficiency and mechanism of peroxymonosulfate (PMS) activation by benzoquinone with different functional groups for sulfamethoxazole degradation. Abstract : Activation of peroxymonosulfate (PMS) by halogenated and methylated quinones for destroying sulfamethoxazole (SMX) was investigated, where 2, 6-dimethyl-1, 4-benzoquinone (DMBQ), 2, 6-dichloro-1, 4-benzoquinone (DCBQ), and tetrafluoro-1, 4-benzoquinone (TFBQ) were chosen as model quinones. The PMS could be activated by halogenated and methylated quinones efficiently for SMX degradation, and the process showed high pH and quinones dependency. Different from PMS activated by ultraviolet (UV), singlet oxygen ( 1 O2 ) instead of hydroxyl radical (˙OH) and sulfate radical (SO4 ˙ − ) was the primary oxidizing species in the activation process. The formation of 1 O2 was confirmed by various quenching studies combined with chemical probes (9, 10-diphenylanthracene (DPA)). By sampling in situ and monitoring in real time, droplet spray ionization mass spectrometry (DSI-MS) was applied to capture and identify the intermediates generated in the activation process. A possible mechanism for PMS activation was proposed accordingly. It was found that a series of reactions between PMS and halogenated/methylated quinones formed a dioxirane intermediate, and the subsequent decomposition of this intermediate produced the 1 O2 . These findings would help to better understand the interactions between PMS and quinones, and provide a novel activator for PMS activation toward environmental contaminants. … (more)
- Is Part Of:
- RSC advances. Volume 9:Issue 47(2019)
- Journal:
- RSC advances
- Issue:
- Volume 9:Issue 47(2019)
- Issue Display:
- Volume 9, Issue 47 (2019)
- Year:
- 2019
- Volume:
- 9
- Issue:
- 47
- Issue Sort Value:
- 2019-0009-0047-0000
- Page Start:
- 27224
- Page End:
- 27230
- Publication Date:
- 2019-08-30
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9ra04789a ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 11625.xml