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Cobalt, cadmium, and lead sorption to hydrous iron oxide: Residence time effect

Journal Article · · Soil Science Society of America Journal; (United States)
;  [1]; ;  [2]
  1. Pacific Northwest Lab., Richland, WA (United States)
  2. Univ. of Montana, Missoula, MT (United States)
The adsorption-desorption of the divalent metal cations (Me[sup 2+]) Co[sup 2+], Cd[sup 2+], and Pb[sup 2+] to hydrous ferric oxide (HFO) was investigated as a function of oxide aging and Me[sup 2+]-oxide residence time. The HFO was produced and stored for up to 86 wk. Periodically, Me[sup 2+] sorption was determined across the pH range of 2.5 to 12. In addition, the Me[sup 2+] ions were contacted with freshly produced HFO and stored at a pH that dictated that 80 to 100% of the Me[sup 2+] would be in the sorbed state; desorbability of the Me[sup 2+] was determined as a function of Me[sup 2+]-oxide residence time. The change in the crystallinity of the HFO as a function of time was also monitored. The HFO aged without the Me[sup 2+] ions displayed no hysteresis between the adsorption-desorption curves and no substantial shifts in fractional Me[sup 2+] adsorption were observed with pH throughout 21 wk of aging. The HFO aged with the Me[sup 2+] ions displayed increasing desorption hysteresis with time for Co[sup 2+] and Cd[sup 2+], but not Pb[sup 2+]. The magnitude of hysteresis followed the order Co > Cd > Pb, which is the inverse of the ionic radii of the metal sorbates. While oxalate-extractable Fe decreased with time during a 20-wk period, powder x-ray diffraction was unchanged during the same period. 38 refs., 11 figs., 2 tabs.
DOE Contract Number:
AC06-76RL01830
OSTI ID:
6707306
Journal Information:
Soil Science Society of America Journal; (United States), Journal Name: Soil Science Society of America Journal; (United States) Vol. 58:6; ISSN 0361-5995; ISSN SSSJD4
Country of Publication:
United States
Language:
English