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Arsenic Incorporation in Synthetic Struvite (NH4MgPO4路6H2O): A Synchrotron XAS and Single-Crystal EPR Study
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  • 作者:Jinru Lin ; Ning Chen ; Yuanming Pan
  • 刊名:Environmental Science & Technology
  • 出版年:2013
  • 出版时间:November 19, 2013
  • 年:2013
  • 卷:47
  • 期:22
  • 页码:12728-12735
  • 全文大小:372K
  • 年卷期:v.47,no.22(November 19, 2013)
  • ISSN:1520-5851
文摘
Struvite, a common biomineral and increasingly important fertilizer recovered from wastewater treatment plants, is capable of sequestering a wide range of heavy metals and metalloids, including arsenic. Inductively coupled plasma mass spectrometric (ICPMS) analyses and microbeam synchrotron X-ray fluororescence (渭-SXRF) mapping show that struvite formed under ambient conditions contains up to 547 卤 15 ppm As and that the uptake of As is controlled by pH. Synchrotron As K-edge XANES spectra measured at 20 K show that As5+ is the predominant oxidation state in struvite, irrespective of Na2HAsO4路7H2O or NaAsO2 as the source for As. Modeling of As K-edge EXAFS data suggest that local structural distortion associated with the substitution of As5+ for P5+ in struvite reaches up to 3.75 脜. Single-crystal electron paramagnetic resonance (EPR) spectra of gamma-ray-irradiated struvite disclose five [AsO3]2鈥?/sup> radicals and one [AsO4]2鈥?/sup> radical. These arsenic-centered oxyradicals are all readily attributed to form from diamagnetic [AsO4]3鈥?/sup> precursors during irradiation, providing further support for exclusive incorporation and local structural expansion beyond the first shell of As5+ at the P site in struvite.

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