| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4425252 | Environmental Pollution | 2011 | 6 Pages |
It has been shown that starch can effectively stabilize nanoscale magnetite particles, and starch-stabilized magnetite nanoparticles (SMNP) are promising for in situ remediation of arsenic-contaminated soils. However, a molecular level understanding has been lacking. Here, we carried out XAFS studies to bridge this knowledge gap. Fe K-edge XAFS spectra indicated that the Fe–O and Fe–Fe coordination numbers of SMNP were lower than those for bare magnetite particles, and these coordination numbers decreased with increasing starch concentration. The decrease in the average coordination number at elevated stabilizer concentration was attributed to the increase in the surface-to-volume ratio. Arsenic K-edge XAFS spectra indicated that adsorbed arsenate on SMNP consisted primarily of binuclear bidentate (BB) complexes and monodentate mononuclear (MM) complexes. More BB complexes (energetically more favorable) were observed at higher starch concentrations, indicating that SMNP not only offered greater adsorption surface area, but also stronger adsorption affinity toward arsenate.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Starch as a stabilizer of magnetite nanoparticles. ► Characterization of starch-stabilized magnetite nanoparticles by XAFS. ► Fe–O and Fe–Fe coordination numbers decreased with starch concentration increasing. ► Ratio of two arsenate complexes adsorbed varied with starch concentration. ► More binuclear bidentate arsenic complexes formed at higher starch concentrations.
