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NAMS 2002 Workshop - ICOM 2008

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macromolecules adsorbed on neighboring silica colloid surface was<br />

hypothesized to be the cause of the greatly enhanced deposition of silica colloids<br />

in the presence of Ca 2+ . Monte-Carlo simulations of the BSA silica system are<br />

currently being performed to better understand how BSA or other<br />

macromolecules affect silica aggregation and deposition behaviors.<br />

Results from these molecular-level characterizations were combined with those<br />

from a series of cross-flow filtration experiments to reveal the mechanisms<br />

involved in the combined effect of model organic and colloidal foulants on NF flux<br />

decline. The enhanced deposition of silica colloids observed in the QCM-D<br />

experiments agreed well with the increased initial flux decline rate during crossflow<br />

filtration of the colloid-organic mixture compared to the additive sum of the<br />

effects of the two individual foulants.<br />

In addition to changing the deposition rate of silica colloids and hence increasing<br />

the initial fouling rate, adsorption of organic macromolecules also alters the<br />

structure of the colloidal cake layer. Transmission electron microscopy (TEM)<br />

imaging of fouled membranes was employed to visualize the structure of the<br />

fouling layer formed with and without the model organic macromolecules. This<br />

effect was manifested at a later stage of the filtration process. Although BSA was<br />

found to significantly increase initial membrane fouling rate, higher quasi-steady<br />

state flux was observed in the presence of BSA due to a more porous fouling<br />

layer.<br />

Results from this study clearly demonstrate that different organic<br />

macromolecules affect colloidal fouling differently. The overall fouling potential of<br />

a complex suspension may not be predicted based on the fouling potential of<br />

each individual foulant.

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