Journal
ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 48, Issue 11, Pages 6342-6349Publisher
AMER CHEMICAL SOC
DOI: 10.1021/es500188t
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Funding
- National Science Foundation [EAR-1251732]
- New York City Louis Stokes Alliance for Minority Participation Program
- Undergraduate Research and Mentoring Education program at Queens College
- U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-98CH10886]
- Directorate For Geosciences [1506653] Funding Source: National Science Foundation
- Division Of Earth Sciences [1506653] Funding Source: National Science Foundation
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Sorption of Zn with struvite was assessed both during and after mineral formation at pH 9.0 for 1-100 mu M (0.065-6.54 mg L-1) aqueous Zn. The Zn loadings of recovered solids were lower when Zn was present during struvite precipitation compared to when Zn was added to struvite-bearing solutions. X-ray absorption fine structure spectroscopy confirmed that Zn added to struvite-bearing solutions at concentrations <= 5 mu M sorbed as both octahedral and tetrahedral complexes (Zn-O 1.98-2.03 angstrom), with evidence for bidentate configuration (Zn-P 3.18 angstrom)., Bidentate complexes were incorporated into the near-surface structure, contributing to distortion of the struvite 113 PO43- band in the Fourier transform infrared spectra. At Zn concentrations >5 mu M, tetrahedral monodentate adsorbates (Zn-O 1.98 angstrom) dominated, transitioning to a Zn-phosphate precipitate at 100 mu M. When Zn is present during struvite precipitation, octahedral monodentate sorbates detected at 1 mu M (Zn-O 2.08-2.10 angstrom; Zn-P 3.60-3.64 angstrom) polymerized at 5-50 mu M, ultimately forming a Zn-hydroxide precipitate at 100 mu M. The lowest initial Zn concentrations (0.065 mg L-1) and resultant solid loadings from precipitation experiments (13 mg kg(-1)) are consistent with those reported for struvite recovered from wastewater, suggesting that similar Zn sorption processes may occur in more complex systems.
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