Synergistic degradation of PNP via coupling H2O2 with persulfate catalyzed by nano zero valent iron. Issue 35 (28th June 2019)
- Record Type:
- Journal Article
- Title:
- Synergistic degradation of PNP via coupling H2O2 with persulfate catalyzed by nano zero valent iron. Issue 35 (28th June 2019)
- Main Title:
- Synergistic degradation of PNP via coupling H2O2 with persulfate catalyzed by nano zero valent iron
- Authors:
- Du, Jiangkun
Wang, Yang
Faheem,
Xu, Tiantian
Zheng, Han
Bao, Jianguo - Abstract:
- Abstract : Simultaneous activation of H2 O2 and persulfate by nanoscaled Fe 0 shows synergistic effect for degradation of p -nitrophenol with generating both hydroxyl and sulfate radicals in a wide initial pH range. Abstract : H2 O2 and persulfate (PDS) activated by iron are attracting much attention due to their strong oxidation capacity for the effective degradation of organic pollutants. However, they face problems such as requiring an acidic reaction pH and difficulty of Fe 2+ regeneration. In this study, the simultaneous activation of H2 O2 and persulfate by nanoscaled zero valent iron (nZVI) was investigated for the degradation of p -nitrophenol (PNP). The nZVI/H2 O2 /PDS oxidation system exhibited significantly higher reactivity toward PNP degradation than the systems with a single oxidant. A synergistic effect was explored between H2 O2 and PDS during nZVI-mediated activation, and the molar ratio of H2 O2 /PDS was a key parameter in optimizing the performance of PNP degradation. The nZVI/H2 O2 /PDS system could function well in a wide pH range, and even 95% PNP was removed at an initial pH 10, thus markedly alleviating the pH limitations of Fenton-like processes. Both hydroxyl radicals and sulfate radicals could be identified during H2 O2 /PDS activation, in which H + produced during PDS decomposition promoted H2 O2 activation. The increase of oxidant concentration could significantly enhance the PNP degradation, while the presence of HCO3 − and HPO4 2− exerted greatAbstract : Simultaneous activation of H2 O2 and persulfate by nanoscaled Fe 0 shows synergistic effect for degradation of p -nitrophenol with generating both hydroxyl and sulfate radicals in a wide initial pH range. Abstract : H2 O2 and persulfate (PDS) activated by iron are attracting much attention due to their strong oxidation capacity for the effective degradation of organic pollutants. However, they face problems such as requiring an acidic reaction pH and difficulty of Fe 2+ regeneration. In this study, the simultaneous activation of H2 O2 and persulfate by nanoscaled zero valent iron (nZVI) was investigated for the degradation of p -nitrophenol (PNP). The nZVI/H2 O2 /PDS oxidation system exhibited significantly higher reactivity toward PNP degradation than the systems with a single oxidant. A synergistic effect was explored between H2 O2 and PDS during nZVI-mediated activation, and the molar ratio of H2 O2 /PDS was a key parameter in optimizing the performance of PNP degradation. The nZVI/H2 O2 /PDS system could function well in a wide pH range, and even 95% PNP was removed at an initial pH 10, thus markedly alleviating the pH limitations of Fenton-like processes. Both hydroxyl radicals and sulfate radicals could be identified during H2 O2 /PDS activation, in which H + produced during PDS decomposition promoted H2 O2 activation. The increase of oxidant concentration could significantly enhance the PNP degradation, while the presence of HCO3 − and HPO4 2− exerted great inhibition. Furthermore, five degradation intermediates of PNP were detected and its degradation pathways in the nZVI/H2 O2 /PDS system were presented. This study reveals that the simultaneous activation of H2 O2 and PDS by nZVI is a promising advanced oxidation tool as an alternative to typical Fenton processes for recalcitrant pollutant removal. … (more)
- Is Part Of:
- RSC advances. Volume 9:Issue 35(2019)
- Journal:
- RSC advances
- Issue:
- Volume 9:Issue 35(2019)
- Issue Display:
- Volume 9, Issue 35 (2019)
- Year:
- 2019
- Volume:
- 9
- Issue:
- 35
- Issue Sort Value:
- 2019-0009-0035-0000
- Page Start:
- 20323
- Page End:
- 20331
- Publication Date:
- 2019-06-28
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9ra02901j ↗
- 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:
- 10968.xml