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Heavy metal adsorption on iron oxide and iron oxide-coated silica ...

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6is further retarded by adsorbed species (Scheinost et al. 2001; Schwertmann et al. 1985;Cornell, 1987; Cornell et al. 1987, 1992). Given localized increases in ferricc<strong>on</strong>centrati<strong>on</strong>s, its precipitati<strong>on</strong> is accompanied by a high partiti<strong>on</strong>ing of trace <str<strong>on</strong>g>metal</str<strong>on</strong>g>s insoils (Manceau et al. 2003). Therefore, goethite <strong>and</strong> HFO have been widely used asmodel sorbents in <str<strong>on</strong>g>adsorpti<strong>on</strong></str<strong>on</strong>g> studies (Cornell <strong>and</strong> Schwertmann, 1996). Dzombak <strong>and</strong>Morel (1990) comprehensively compiled <strong>and</strong> modeled <str<strong>on</strong>g>metal</str<strong>on</strong>g> <str<strong>on</strong>g>adsorpti<strong>on</strong></str<strong>on</strong>g> <strong>on</strong> HFO usingthe diffuse double layer model. However, since 1990, spectroscopic evidence has provento be critical in mechanistic model development.In natural aquatic envir<strong>on</strong>ments, many reacti<strong>on</strong>s such as dissoluti<strong>on</strong>, <str<strong>on</strong>g>adsorpti<strong>on</strong></str<strong>on</strong>g>,precipitati<strong>on</strong>, <strong>and</strong> colloidal adhesi<strong>on</strong> result in multi-comp<strong>on</strong>ent solids with bulk <strong>and</strong>surface characteristics different from the original pure phases (Anders<strong>on</strong> <strong>and</strong> Benjamin,1990). Specifically, <strong>oxide</strong> mineral coatings are often observed in soils <strong>and</strong> sediments(Ryan <strong>and</strong> Gschwend, 1994; Cost<strong>on</strong> et al. 1995; Wang et al. 1993). For example, Ryan<strong>and</strong> Gschwend (1994) found that in oxic sediments, quartz grains are <strong>coated</strong> by colloidalkaolinite <strong>and</strong> microcrystalline ir<strong>on</strong> (III) <strong>oxide</strong>, primarily goethite (a-FeOOH) at 39 ± 2μmol Fe g-1 sediment (0.22% by weight). Cost<strong>on</strong> et al. (1995) reported that in a shallow,unc<strong>on</strong>fined aquifer of glacial out wash, s<strong>and</strong> <strong>and</strong> gravel were extensively <strong>coated</strong> with Al<strong>and</strong>Fe-bearing minerals <strong>and</strong> that the ir<strong>on</strong> c<strong>on</strong>centrati<strong>on</strong>s ranged between 0.0736 <strong>and</strong> 4.96mg Fe g-1 s<strong>and</strong>. Ir<strong>on</strong> <strong>oxide</strong> coatings were also found <strong>on</strong> ped surfaces <strong>and</strong> pores of paddy<strong>and</strong> n<strong>on</strong>-paddy soils at c<strong>on</strong>centrati<strong>on</strong>s of 10 to 44 mg Fe g -1 soil <strong>and</strong> were characterizedas ferrihydrite, lepidocrocite, <strong>and</strong> goethite (Wang et al. 1993). Many studies have shownthe importance of these surface coatings in c<strong>on</strong>trolling <str<strong>on</strong>g>metal</str<strong>on</strong>g> distributi<strong>on</strong> in soils <strong>and</strong>sediments (Edwards <strong>and</strong> Benjamin, 1989; Cost<strong>on</strong> et al. 1995; Zachara et al. 1995; Fuller

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