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Stability of Fe- and Mn-(oxyhydr)oxides in Common Soil Dispersion Solutions

Authors
Manh, Phung N.Khan, Moonis AliJeon, Byong HunKim, Jae GonLee, Giehyeon
Issue Date
May-2011
Publisher
SPRINGER
Keywords
Dispersion reagent; Fe oxides; Mn oxides; Pyrophosphate; Soil dispersion
Citation
WATER AIR AND SOIL POLLUTION, v.217, pp.677 - 687
Indexed
SCIE
SCOPUS
Journal Title
WATER AIR AND SOIL POLLUTION
Volume
217
Start Page
677
End Page
687
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/168455
DOI
10.1007/s11270-010-0619-2
ISSN
0049-6979
Abstract
Soil dispersion is a prerequisite process for the separation of metal oxides from bulk soil when magnetic separation is employed to enhance the efficiency for soil treatment. This study examined the stability of goethite, hematite, birnessite, and manganite in common dispersion solutions. The stability of pH in the oxide suspension decreased in the order carbonate (50 mM Na2CO3) ˃ pyrophosphate (50 mM Na4P2O7) ˃ simple alkaline (1 mM NaOH) solutions regardless of the oxides. Dissolution of the four oxides was negligible in the carbonate and the simple alkaline solutions. In the pyrophosphate solutions, however, the oxides were subject to ligand-promoted dissolution by pyrophosphate ion. The extent of dissolution was highest for goethite followed by manganite, hematite, and birnessite. Dissolved Fe and Mn concentrations reached 68.3 and 4.1 mu M for goethite and manganite suspensions, respectively, in 21 days with 5 mM pyrophosphate. Higher pyrophosphate concentrations (up to 150 mM) did not substantially affect the extent of ligand-promoted dissolution due to the limited surface sites of the oxides. The results of this study suggest that the carbonate solution would be more desirable than the simple alkaline or the pyrophosphate solution for soil dispersion in the presence of common Fe or Mn oxides.
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COLLEGE OF ENGINEERING (DEPARTMENT OF EARTH RESOURCES AND ENVIRONMENTAL ENGINEERING)
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