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Phosphorous recovery from water via batch adsorption enrichment combined with struvite crystallization in a fluidized bed reactor.

Authors :
Bah, Amadu T.
Shen, Ziyi
Yan, Junna
Li, Feihu
Source :
Journal of Environmental Chemical Engineering; Jun2023, Vol. 11 Issue 3, pN.PAG-N.PAG, 1p
Publication Year :
2023

Abstract

To assess the feasibility of recovering P from water by combining batch adsorption enrichment with struvite crystallization, we prepared four ternary layered double hydroxides (LDHs) with P-preferring elements (i.e., zirconium (Zr) or lanthanum (La)) via a facile coprecipitation method, and evaluated their performance in recovering P from water, particularly in enriching P from a low-level P solution. We find that all ternary LDHs demonstrate remarkably high P adsorption capacities, e.g., 1029.3 mg PO 4 <superscript>3−</superscript> g<superscript>−1</superscript> for ZnAlLa, outperforming other LDHs reported so far. Microstructural analyses show that the P uptake mechanisms are attributable to anion exchange, surface complexation and electrostatic attraction. Results of recycling tests indicate that all LDHs present good enrichment for P. Besides, more than 96% of phosphorus in the P-enriched eluates can be efficiently reclaimed via struvite crystallization in a fluidized bed reactor. These findings demonstrate the feasibility of combining adsorption enrichment with struvite crystallization for P recovery. [Display omitted] • Four ternary LDHs with P-preferring elements (Zr or La) were prepared. • These ternary LDHs show high stability against either acidic or basic solution. • These LDHs exhibit superior adsorption capacities of P compared to other LDHs. • P-enriched eluates can be obtained from consecutive adsorption-desorption cycles. • P in the eluates can be efficiently recovered via struvite crystallization in an FBR. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
22133437
Volume :
11
Issue :
3
Database :
Supplemental Index
Journal :
Journal of Environmental Chemical Engineering
Publication Type :
Academic Journal
Accession number :
164346782
Full Text :
https://doi.org/10.1016/j.jece.2023.110180