Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/90060
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Title: Transformation of Fe-P complexes in bioreactors and P recovery from sludge : investigation by XANES spectroscopy
Authors: Li, RH
Cui, JL 
Hu, JH
Wang, WJ
Li, B
Li, XD 
Li, XY
Issue Date: 7-Apr-2020
Source: Environmental science & technology, 7 Apr. 2020, v. 54, no. 7, p. 4641-4650
Abstract: The transformation of Fe-P complexes in bioreactors can be important for phosphorus (P) recovery from sludge. In this research, X-ray absorption near-edge structure analysis was conducted to quantify the transformation of Fe and P species in the sludge of different aging periods and in the subsequent acidogenic cofermentation for P recovery. P was readily removed from wastewater by Fe-facilitated coprecipitation and adsorption and could be extracted and recovered from sludge via acidogenic cofermentation and microbial iron reduction with food waste. The fresh Fe-based sludge mainly contained fresh ferrihydrite and amorphous FePO4 with sufficient accessible surface area, which was favorable for Fe-P mobilization and dissolution via microbial reaction. Ferric iron dosed into wastewater underwent rapid hydrolysis, clustering, aggregation, and slow crystallization to form hydrous iron oxides (HFO) with various complicated structures. With the aging of sludge in bioreactors, the HFO densified into phases with much reduced surface area and reactivity (e.g., goethite), which greatly increased the difficulty of P release and recovery. Thus, aging of P-containing sludge should be minimized in wastewater treatment systems for the purpose of P recovery.
Publisher: American Chemical Society
Journal: Environmental science & technology 
ISSN: 0013-936X
EISSN: 1520-5851
DOI: 10.1021/acs.est.9b07138
Rights: © 2020 American Chemical Society
This document is the Accepted Manuscript version of a Published Work that appeared in final form in Environmental Science & Technology, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://pubs.acs.org/doi/abs/10.1021/acs.est.9b07138
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