Theory and Methodology for Determining Nanoparticle Affinity for Heteroaggregation in Environmental Matrices Using Batch Measurements

Published

Journal Article

© Copyright 2014, Mary Ann Liebert, Inc. 2014. In this study, we present a method for determining the relative affinity of nanoparticles (NPs) for an ensemble of other particles in a complex, heterogeneous suspension. We evaluated this method for NPs heteroaggregating with suspended solids present in activated sludge. A relationship was derived between the heterogeneous affinity coefficient, α, and measurements over time of the distribution coefficient, γ, of NPs measured in supernatant versus those removed by heteroaggregation and subsequent settling. Application of this method, which uses a mathematical relationship to determine α from experimentally measured γ values, to a series of metal and metal oxide NPs heteroaggregated with activated sludge indicated a relative affinity in the order of pristine CeO2, TiO2 NPs, and ZnO NPs>Ag(0) NPs surface-modified with polyvinylpyrrolidone (PVP)>citrate-functionalized CeO2 NP>Ag(0) NPs surface-modified with gum arabic. This trend in relative affinity followed the observed trend in removal such that higher affinity corresponded to higher removals of NPs. Values of α were calculated from measured relative affinities using average diameter and concentration of the activated sludge particles. The value calculated for PVP-stabilized Ag(0) NPs was comparable to a value previously reported for the attachment of these same NPs to a biofilm. Calculations also yielded size dependence of α in the case of the two Ag(0) evaluated that may be linked to NP dissolution.

Full Text

Duke Authors

Cited Authors

  • Barton, LE; Therezien, M; Auffan, M; Bottero, JY; Wiesner, MR

Published Date

  • July 1, 2014

Published In

Volume / Issue

  • 31 / 7

Start / End Page

  • 421 - 427

Electronic International Standard Serial Number (EISSN)

  • 1557-9018

International Standard Serial Number (ISSN)

  • 1092-8758

Digital Object Identifier (DOI)

  • 10.1089/ees.2013.0472

Citation Source

  • Scopus