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Adsorption-dissolution reactions affecting the distribution and stability of Co[sup II]EDTA in ion oxide-coated sand

Journal Article · · Environmental Science and Technology; (United States)
DOI:https://doi.org/10.1021/es00058a024· OSTI ID:7124611
; ;  [1]
  1. Pacific Northwest Lab., Richland, WA (United States)

The time-variant chemical behavior of Co[sup II]EDTA (and other metal-EDTA complexes) was investigated in suspensions of iron oxide-coated sand to identify equilibrium and kinetic reactions that control the mobility of Me[sup II]-EDTA complexes in subsurface environments. Batch experiments were conducted to evaluate the adsorption as a function of pH, concentration, and time and to quantify the rate-controlling step(s) of dissolution of the iron oxide by EDTA complexes. Ionic Co[sup 2+] exhibited typical cation-like adsorption, whereas Me[sup II]EDTA adsorption was ligand-like, increasing with decreasing pH. Adsorption isotherms for all reactive species exhibited Langmuir behavior, with site saturation occurring at molar values of <0.5% of Fe[sub tot]. The adsorption of Me[sup II]EDTA enhanced the apparent solubility of the iron oxide phase, which destabilized the Co[sup II]EDTA complex, liberating Co[sup 2+] and Fe[sup III]EDTA. The dissolution rate was an order of magnitude slower at pH 6.5 than at pH 4.5 and was influenced by the re-adsorption of solubilized Fe[sup III]EDTA. Two multireaction kinetic models were developed that each included Langmuir adsorption for Co[sup 2+] and metal-EDTA species but differed in their depiction of the dissolution mechanism (i.e., ligand-versus proton-promoted dissolution). 45 refs., 8 figs., 6 tabs.

DOE Contract Number:
AC06-76RL01830
OSTI ID:
7124611
Journal Information:
Environmental Science and Technology; (United States), Journal Name: Environmental Science and Technology; (United States) Vol. 28:9; ISSN ESTHAG; ISSN 0013-936X
Country of Publication:
United States
Language:
English

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