Chemical Fate of Cerium Oxide Nanoparticles in Soils.
Poster Number 1911
Tuesday, November 5, 2013
Tampa Convention Center, East Hall, Third Floor
Yuji Arai1, Allison Rick VandeVoort2 and Jessica Dahle2, (1)Clemson University, Urbana, IL (2)Clemson University, Clemson, SC
Cerium-based compounds such as CeO2 nanoparticles (NP) have received much attention in the last several years due to their popular applications in industrial and commercial uses. There is a growing concern about the environmental fate of released CeO2 NPs, particularly their unintended impact in aquatic and terrestrial environments. To understand the chemical fate of CeO2 NPs in soils, reactivity of CeO2 NPs in agricultural soils (Taccoa entisols) were studied as a function of particle size (33 and 78 nm), redox condition, and aging time. Batch dissolution experiments show that CeO2 NPs were only soluble at pH <5 under the oxic condition. The distribution coefficient for small and large NPs ranged from 5,101 to 102,039 L kg-1, and from 5,356 to 71,427 L kg-1, respectively, showing the strong sorption CeO2 NPs in soils that is independent of particle size. Furthermore, changes in chemical state of Ce (reduction of Ce(IV) to Ce(III)) was observed after 30d in reduced soils for small CeO2 NPs. However, there was no significant changes in chemical speciation of Ce in the large CeO2 NP reacted soils. The Ce chemical speciation and reactivity of CeO2 in soils might be important in predicting the fate of CeO2NPs to environment.