The activated iron system for phosphorus recovery in aqueous environments. (April 2018)
- Record Type:
- Journal Article
- Title:
- The activated iron system for phosphorus recovery in aqueous environments. (April 2018)
- Main Title:
- The activated iron system for phosphorus recovery in aqueous environments
- Authors:
- Wan, Jun
Jiang, Xiaoqing
Zhang, Tian C.
Hu, Jiong
Richter-Egger, Dana
Feng, Xiaonan
Zhou, Aijiao
Tao, Tao - Abstract:
- Abstract: Finding a good sorbent for phosphorus (P) recovery from the aquatic environment is critical for preventing eutrophication and providing P resources. The activated iron system (mainly consisted of zero-valent iron (ZVI), Fe3 O4 and Fe 2+ ) has been reported to exhibit a favorable performance towards various contaminants in wastewater, but its effect on P recovery has not been studied systematically. In this study, we used Fe 2+ -nitrate pretreatment reaction to prepare the activated iron system and then applied it to P recovery. Results show that more than 99% P was removed from water in 60 min; co-existing anions (NO3 −, Cl − and SO4 2− ) and natural organic matter (NOM) had little effect on P removal. The P removal capacity of activated iron system is very high compared with currently reported sorbents. Externally-supplied Fe 2+ plays an important role on P removal in the system. Regeneration study shows that the activated iron system exhibited stable P recovery ability by using 0.1 M NaOH solution. Various methods were applied to characterize the ZVI and iron corrosion, and results conclude that sorption precipitation, and co-precipitation contribute to P removal. This method will be promising and have an application potential in the field for efficient and cost-effective recovery of P with cheap microscale zero valent iron. Highlights: Activated iron system was prepared using nitrate and Fe 2+ to pretreat Fe 0 . Co-existing anions and NOM had little effect on PAbstract: Finding a good sorbent for phosphorus (P) recovery from the aquatic environment is critical for preventing eutrophication and providing P resources. The activated iron system (mainly consisted of zero-valent iron (ZVI), Fe3 O4 and Fe 2+ ) has been reported to exhibit a favorable performance towards various contaminants in wastewater, but its effect on P recovery has not been studied systematically. In this study, we used Fe 2+ -nitrate pretreatment reaction to prepare the activated iron system and then applied it to P recovery. Results show that more than 99% P was removed from water in 60 min; co-existing anions (NO3 −, Cl − and SO4 2− ) and natural organic matter (NOM) had little effect on P removal. The P removal capacity of activated iron system is very high compared with currently reported sorbents. Externally-supplied Fe 2+ plays an important role on P removal in the system. Regeneration study shows that the activated iron system exhibited stable P recovery ability by using 0.1 M NaOH solution. Various methods were applied to characterize the ZVI and iron corrosion, and results conclude that sorption precipitation, and co-precipitation contribute to P removal. This method will be promising and have an application potential in the field for efficient and cost-effective recovery of P with cheap microscale zero valent iron. Highlights: Activated iron system was prepared using nitrate and Fe 2+ to pretreat Fe 0 . Co-existing anions and NOM had little effect on P removal. Fe 2+ plays an important role in P removal. Activated Iron system is a promising technology for P removal and recovery. … (more)
- Is Part Of:
- Chemosphere. Volume 196(2018)
- Journal:
- Chemosphere
- Issue:
- Volume 196(2018)
- Issue Display:
- Volume 196, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 196
- Issue:
- 2018
- Issue Sort Value:
- 2018-0196-2018-0000
- Page Start:
- 153
- Page End:
- 160
- Publication Date:
- 2018-04
- Subjects:
- Activated iron -- Phosphorus recovery -- Zero valent iron -- Magnetite -- Ferrous ion
Pollution -- Periodicals
Pollution -- Physiological effect -- Periodicals
Environmental sciences -- Periodicals
Atmospheric chemistry -- Periodicals
551.511 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00456535/ ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.chemosphere.2017.12.140 ↗
- Languages:
- English
- ISSNs:
- 0045-6535
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3172.280000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 23135.xml