Premium
Characterizing heavy‐metal adsorption on oxides and oxyhydroxides
Author(s) -
SPARK K.M.,
JOHNSON B.B.,
WELLS J.D.
Publication year - 1995
Publication title -
european journal of soil science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.244
H-Index - 111
eISSN - 1365-2389
pISSN - 1351-0754
DOI - 10.1111/j.1365-2389.1995.tb01358.x
Subject(s) - adsorption , chemistry , ionic strength , metal , goethite , inorganic chemistry , substrate (aquarium) , precipitation , metal ions in aqueous solution , aqueous solution , organic chemistry , oceanography , physics , meteorology , geology
Summary Adsorption of Cu(II), Zn(II), Co(II) and Cd(II) on three different substrates: goethite, alumina and silica, was investigated over the pH range from 3.5 to 10. The consistent variation in the pH at which 50% of the metal is adsorbed (pH 50 ) indicates that the identity of the adsorbing ion is the principal factor determining the pH range over which adsorption occurs. However, the nature of the substrate does play a lesser role. The proton coefficient, χ, ranged from about 0.5 to 1.8, and was correlated with the difference between pH 50 and the pH for 50% precipitation. It is suggested that for most metal‐substrate systems, for which χ is about 1, MOH + plays a dominant role in adsorption. Increasing the substrate concentration decreased pH 50 for adsorption of metals on goethite, but there was little change in χ. The change in pH 50 was inversely related to χ. While the effect of the nature and concentration of the background electrolyte on Cu(II), Zn(II) and Co(II) adsorption depended on the substrate, increased ionic strength was found to decrease Cd(II) adsorption on all substrates.