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This page contains a single entry from the blog posted on March 22, 2013 11:53 AM.

The previous post in this blog was CBEE travels to Isongo, Kenya for a clean water project with EWB-UMBC.

The next post in this blog is Ph.D. Dissertation Defense by John Bendick (Wed. 4/17).

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PhD Dissertation Defense by Angele Kwimi (Mar. 29, 8:30am)

When: Friday, March 29th , 2013, 8:30am
Where: TRC 206.

Department of Chemical, Biochemical, and Environmental Engineering

Student: Angele Kwimi

Dissertation title:

Interaction of As(III), As(V) and PO4 with Fe Oxide Impregnated Activated Carbons: Modeling Multisorbate Adsorption using the Surface Complexation Approach


Abstract:

The adsorption behavior of As (III) as a function of pH on an iron oxide impregnated activated carbon (FeAC, 7% Fe(III) amorphous iron-oxide) at different adsorbate/adsorbent concentrations was modeled using the surface complexation modeling approach. The surface complexation constants developed from single sorbate experiments successfully predicted competition between As(V) and As(III) and the surface complexation modeling (SCM) predictions were verified experimentally. The monoprotic surface site representation described the experimental data better than the diprotic representation. Based on surface complexation modeling simulations, the effect of As(V) on As(III) removal was greater than As(III) on As(V) removal. As(III)à As(V) was observed beginning at pH = 8. As(V) and As(III) removal by an iron-oxide impregnated carbon (L-Act, 9% Fe(III) amorphous iron-oxide) over a range of environmental conditions using SCM approach were also investigated. L-Act surface complexation constants determined from single adsorbate systems were effectively used to predict pH dependent removal of As(V), As(III) and PO4 across a range of adsorbent/adsorbate ratios in single, binary and tertiary adsorbate systems and from a ‘National Sanitation Foundation’ challenge water. As(V) and PO4 complexes were modeled as bidentate binuclear species at low pH and monodentate species at high pH; using the two monoprotic surface site representations with the diffuse electric double layer model (MDLM). For the bidentate-binuclear complexation, two approaches based on the value of the exponent on [NOH] in the mass action law (n = 1 or 2), produced similarly good results. The effect of As(V) on As(III) removal was greater than As(III) on As(V). In the tertiary system, the effect of PO4 on As(III) removal was more pronounced than on As(V) removal. As(III) à As(V) was observed for L-Act beginning at pH = 8.5. The MDLM successfully predicted As(III)/As(V)/PO4 behavior for other iron-based adsorbents that were reported in the literature. The MDLM was also used to address other arsenic-related environmental questions.