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Nanoparticle Transport, Aggregation, and Deposition  277

        different evolution in the size distribution produced in each instance
        (Figure 7.28).
          The unique aggregation results found observed for the various poly-
        saccharides in Figure 7.28 may be traced to their different molecular
        chemistries and do not demonstrate a clear size effect. In this example,

        the acetate groups (CH COO ) that are characteristic of the MWAP71
                              3
        and gellan seem to promote aggregation. Conversely, no trend was evi-
        denced with regards to molecular size and the degree of aggregation.
        Indeed, the smaller MWAP71 produced a similar degree of aggregation
        as the larger gellan, while less severe aggregation was seen with the dex-
        tran. While not considered as conclusive evidence, these results suggest
        that chemical interactions and not purely size must be considered when
        evaluating nanoparticle interactions with complex molecules like poly-
        sacharrides. In other words, we see that chemistry, and not size alone,
        continues to be important.
          Beyond merely altering particle surface charge, adsorption of NOM
        may affect the type of interactions that occur between particles in water.
        For example, the thickness of the adsorbed organic layer may, under spe-
        cific conditions (high salinity), exceed the thickness of the diffuse double
        layer, ultimately altering the nature of the interfacial interactions
        (Figure 7.29) [86]. Under conditions of high ionic strength, as two
        nanoparticles approach one another the interfacial interaction would
        more likely be determined by chemical interactions between the









                                  Low
                                 salinity











                                  High     Figure 7.29  Illustration showing
                                 salinity  the diffuse double layer and
                                           adsorbed organic layer thick-
                                           ness at low and high salt con-
                                           centrations.
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