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

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585.2.5 Surface Charge Distributi<strong>on</strong>Potentiometric titrati<strong>on</strong>s were c<strong>on</strong>ducted to verify the PZC of Alfa Aesar <strong>and</strong> US <strong>silica</strong>.Usually titrati<strong>on</strong>s can be performed with either acid or base. In acid titrati<strong>on</strong>s, the <strong>silica</strong>suspensi<strong>on</strong> needs to be adjusted to a higher pH <strong>and</strong> is then titrated with an acid. Thisprocess is reversed when the titrati<strong>on</strong> is c<strong>on</strong>ducted with base.In this study, titrati<strong>on</strong> of <strong>silica</strong> was initially performed with acid (HNO3). Theresulting PZC of Alfa Aesar <strong>and</strong> US <strong>silica</strong> was about 5.0 <strong>and</strong> 4.9, respectively, <strong>and</strong> arehigher than that of other studies listed in Table 5.4. These differences which may becaused by the dissoluti<strong>on</strong> of <strong>silica</strong>. Yates (1975) studied the influence of <strong>oxide</strong> solubilityduring a titrati<strong>on</strong> in determining <strong>oxide</strong> surface charge. He found that the dissoluti<strong>on</strong> doesnot affect titrati<strong>on</strong>s below pH 7, because the neutral species Si(OH)4 ° predominates.However, the hydrolysis of Si(OH)4° occurs above this pH c<strong>on</strong>suming Off (has a buffereffect around its pKa1, 9.46, Yates, 1975) <strong>and</strong> thus affecting the titrati<strong>on</strong> procedure.When the effect of dissoluti<strong>on</strong> is not corrected in the calculati<strong>on</strong>, the surface chargeincreases. Therefore, the c<strong>on</strong>sumpti<strong>on</strong> of O1-1- should be c<strong>on</strong>sidered when performingtitrati<strong>on</strong>s with acid, especially when the <strong>silica</strong> c<strong>on</strong>centrati<strong>on</strong> in the suspensi<strong>on</strong> is low <strong>and</strong>surface dissoluti<strong>on</strong> is potentially a significant fracti<strong>on</strong> of the total <strong>silica</strong> present (2 g L -1 inthis study).Ultimately, base titrati<strong>on</strong>s were used to determine the surface charge distributi<strong>on</strong>of <strong>silica</strong> samples. The PZC value of <strong>silica</strong> samples in this study is 2.85 (Figure 5.10) <strong>and</strong>is c<strong>on</strong>sistent with other studies. The acid-washed US <strong>silica</strong> sample has less than 1.5%(mass) impurities as seen in Table 5.3; nevertheless, these impurities are likely <strong>on</strong> thesurface affecting the surface charge.

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