Heavy metal adsorption on iron oxide and iron oxide-coated silica ...
Heavy metal adsorption on iron oxide and iron oxide-coated silica ...
Heavy metal adsorption on iron oxide and iron oxide-coated silica ...
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147<str<strong>on</strong>g>adsorpti<strong>on</strong></str<strong>on</strong>g> affinity of the <strong>coated</strong> media is str<strong>on</strong>gly influenced by goethite coatings.Similar results were observed in Zn <str<strong>on</strong>g>adsorpti<strong>on</strong></str<strong>on</strong>g> edges (Figure 10.2). Percent Znsorbed increases after pH 5 for <strong>silica</strong> <strong>and</strong> the edge jump was over a broad pH range from4 to 8 for GACS. The goethite coatings present a higher affinity for Zn than <strong>silica</strong> <strong>and</strong>the pH values at which 50% <str<strong>on</strong>g>adsorpti<strong>on</strong></str<strong>on</strong>g> occurs lowered by 1.7 pH units at IS 10 -3 <strong>and</strong> 1.4pH units at IS 10 -2. Both systems show i<strong>on</strong>ic strength effects <strong>on</strong> Zn sorpti<strong>on</strong>; therefore,<strong>silica</strong> again appears to dominate electrostatic interacti<strong>on</strong>s of the <strong>coated</strong> media.Overall, similar to prot<strong>on</strong> <str<strong>on</strong>g>adsorpti<strong>on</strong></str<strong>on</strong>g>, both comp<strong>on</strong>ents of the <strong>coated</strong> <strong>silica</strong> affectNi <strong>and</strong> Zn <str<strong>on</strong>g>adsorpti<strong>on</strong></str<strong>on</strong>g>. By distinguishing inner- <strong>and</strong> outer-sphere <str<strong>on</strong>g>adsorpti<strong>on</strong></str<strong>on</strong>g> with XAS,the triple layer model is expected to be more advantageous in modeling than other modelssuch as CCM, DLM, <strong>and</strong> Stern model. This modeling work al<strong>on</strong>g with XAS isrecommended in future research.10.2 Ni <strong>and</strong> Zn Adsorpti<strong>on</strong> IsothermsNi <str<strong>on</strong>g>adsorpti<strong>on</strong></str<strong>on</strong>g> isotherms with <strong>silica</strong>, GACS, <strong>and</strong> goethite were c<strong>on</strong>ducted from pH 4 to 7under i<strong>on</strong>ic strength 10-3. Results (Figure 10.3) indicate that Ni <str<strong>on</strong>g>adsorpti<strong>on</strong></str<strong>on</strong>g> to thesesorbents increases in the order of <strong>silica</strong> < GACS < goethite. For <strong>silica</strong> (Figure 10.4a), pH4 <strong>and</strong> 5 isotherms have slopes approximately equal to <strong>on</strong>e below a Ni c<strong>on</strong>centrati<strong>on</strong> of10-7 M <strong>and</strong> less than <strong>on</strong>e between 10-7-10-6 M. Saturati<strong>on</strong> of the higher affinity sites(approximately 5 x10 -9 mole Ni g-1 <strong>silica</strong>) may have occurred. The shape of the pH 4 <strong>and</strong>5 isotherms at Ni c<strong>on</strong>centrati<strong>on</strong>s greater than 10 -6 M is c<strong>on</strong>sistent with presence of alower affinity site <strong>and</strong>/or formati<strong>on</strong> of Ni polymer (Dzombak <strong>and</strong> Morel, 1990; Katz <strong>and</strong>Hayes, 1995b; Hayes <strong>and</strong> Katz, 1996). However, there was no indicati<strong>on</strong> of low affinity