Impact of inorganic ions and natural organic matter on arsenates removal by ferrate(VI): Understanding a complex effect of phosphates ions
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
29804022
DOI
10.1016/j.watres.2018.05.024
PII: S0043-1354(18)30390-7
Knihovny.cz E-zdroje
- Klíčová slova
- Arsenates, Fe(VI), Natural ions, Oxidation, Phosphates, Reaction mechanism, Water treatment,
- MeSH
- adsorpce MeSH
- arseničnany chemie MeSH
- chemické látky znečišťující vodu chemie MeSH
- chloridy chemie MeSH
- čištění vody metody MeSH
- dusičnany chemie MeSH
- fosfáty chemie MeSH
- huminové látky * MeSH
- koncentrace vodíkových iontů MeSH
- sírany chemie MeSH
- spektroskopie Mossbauerova MeSH
- uhličitany chemie MeSH
- železité sloučeniny chemie MeSH
- železo chemie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- arseničnany MeSH
- chemické látky znečišťující vodu MeSH
- chloridy MeSH
- dusičnany MeSH
- ferrate ion MeSH Prohlížeč
- ferric oxide MeSH Prohlížeč
- fosfáty MeSH
- huminové látky * MeSH
- sírany MeSH
- uhličitany MeSH
- železité sloučeniny MeSH
- železo MeSH
Arsenic compounds are carcinogenic to humans and are typically removed from contaminated water using various sorbents. The ionic composition plays a significant role in arsenate removal efficiency during the process of water remediation. Here, we quantify the effects of natural ions (chlorides, nitrates, carbonates, sulfates, and phosphates) and humic acid on the removal of arsenates by ferrate(VI) at pH = 6.6. In the experiments, the initial concentration of arsenates was 10 mg L-1 (as As) and the concentrations of ions varied in the range from 5 to 100 mg L-1 of element in ionic form and humic acid. The achieved results show that only phosphate ions had principle influence on the efficiency of arsenate removal by ferrate(VI). The effect of phosphates was elucidated by applying transmission electron microscopy, energy-dispersive X-ray spectroscopy, and low temperature in-field 57Fe Mössbauer spectroscopy to solid samples, prepared under different weight ratios of ferrate(VI), arsenates, and phosphates. These results show three crucial effects of phosphates on the arsenate removal mechanisms. At low P:As weight ratio (up to 1:1), the incorporation of arsenate ions into the crystalline structure of γ-Fe2O3/γ-FeOOH nanoparticles was found to be suppressed by the presence of phosphates. Thus, arsenates were mainly adsorbed onto the surface of γ-Fe2O3/γ-FeOOH nanoparticles. Further increase in the P:As weight ratio (more than 1:1) resulted in the competition between arsenates and phosphates sorption. With the increased concentration of phosphate ions, the number of arsenates on the surface of γ-Fe2O3/γ-FeOOH nanoparticles was reduced. Finally, the complexation of iron(III) ions with phosphate ions occurred, leading to a decrease in the arsenates removal efficiency, which resulted from a lower content of precipitated γ-Fe2O3/γ-FeOOH nanoparticles. All these aspects need to be considered prior to application of ferrate(VI) for arsenates removal in real natural waters.
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