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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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151sites in the pH 6 <strong>and</strong> 7 isotherms. For these two c<strong>on</strong>diti<strong>on</strong>s, the isotherm appearsapproach saturati<strong>on</strong> (approximately 5x10 -7 mole Ni g -1 <strong>silica</strong>) for Ni c<strong>on</strong>centrati<strong>on</strong>sgreater than 10-6 M <strong>and</strong> less than 10 -4 M. Interestingly, using a n<strong>on</strong>-electrostatic model,Delolme et al. (2004) obtained an optimized SiOH site c<strong>on</strong>centrati<strong>on</strong> of 8x10 -7 mole g-1for a natural s<strong>and</strong> with a diameter of 0.3 to 2 mm, similar to that used in this study. The<strong>silica</strong> isotherms overlap at Ni c<strong>on</strong>centrati<strong>on</strong>s greater than 10 -4 M; this may suggestformati<strong>on</strong> of Ni polymers instead of a lower affinity site. The Ni/<strong>silica</strong> <str<strong>on</strong>g>adsorpti<strong>on</strong></str<strong>on</strong>g>isotherm seems to reveal more informati<strong>on</strong> than the <str<strong>on</strong>g>adsorpti<strong>on</strong></str<strong>on</strong>g> edges about surface sitessuggesting more than <strong>on</strong>e mechanism. Coupled with electrophoretic informati<strong>on</strong>, Kuanet al. (2004) modeled Al(III) <str<strong>on</strong>g>adsorpti<strong>on</strong></str<strong>on</strong>g> to an amorphous <strong>silica</strong> reas<strong>on</strong>ably well with asurface complexati<strong>on</strong>/precipitati<strong>on</strong> model over Al(III) c<strong>on</strong>centrati<strong>on</strong>s ranging from 10 4 ' 5to 10-2 M. The authors proposed Al(H2O)6 3+ complex at low pH (

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