Dissemin is shutting down on January 1st, 2025

Published in

American Chemical Society, Environmental Science and Technology, 22(47), p. 12844-12851, 2013

DOI: 10.1021/es402880u

Links

Tools

Export citation

Search in Google Scholar

Surface Charge Controls the Fate of Au Nanorods in Saline Estuaries

This paper is available in a repository.
This paper is available in a repository.

Full text: Download

Green circle
Preprint: archiving allowed
  • Must obtain written permission from Editor
  • Must not violate ACS ethical Guidelines
Orange circle
Postprint: archiving restricted
  • Must obtain written permission from Editor
  • Must not violate ACS ethical Guidelines
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO

Abstract

This work reports the distribution of negatively charged, gold core nanoparticles in a model marine estuary as a function of time. A single dose of purified polystyrene sulfonate (PSS) coated gold nanorods was added to a series of three replicate estuarine mesocosms to emulate an abrupt nanoparticle release event to a tidal creek of a Spartina-dominated estuary. The mesocosms contained several phases that were monitored: seawater, natural sediments, mature cordgrass, juvenile northern quahog clam, mud snails and grass shrimp. Aqueous nanorod concentrations rose rapidly upon initial dosing then fell to stable levels over the course of approximately 50 hr, after which they remained stable for the remainder of the experiment (41 days total). The concentration of nanorods rose in all other phases during the initial phase of the experiment, however some organisms demonstrated depuration over extended periods of time (100 hr +), even in the dosed tanks. Clams and biofilm samples were also removed from the contaminated tanks post exposure to monitor their depuration in pristine seawater. The highest net uptake of gold (mass normalized) occurred in the biofilm phase during the first 24 hrs, after which it was stable (to the 95% level of confidence) throughout the remainder of the exposure experiment. The results are compared against a previous study of positively charged nanoparticles of the same size to parameterize the role of surface charge in determining nanoparticle fate in complex aquatic environments.