Stability and Aggregation of Metal Oxide Nanoparticles in Natural Aqueous Matrices

被引:1127
作者
Keller, Arturo A. [1 ]
Wang, Hongtao [1 ,2 ]
Zhou, Dongxu [1 ]
Lenihan, Hunter S. [1 ]
Cherr, Gary [3 ]
Cardinale, Bradley J. [1 ]
Miller, Robert [1 ]
Ji, Zhaoxia [4 ]
机构
[1] Univ Calif Santa Barbara, Santa Barbara, CA 93106 USA
[2] Tongji Univ, Shanghai 200092, Peoples R China
[3] Univ Calif Davis, Davis, CA 95616 USA
[4] Univ Calif Los Angeles, Los Angeles, CA USA
基金
美国国家科学基金会;
关键词
IONIC-STRENGTH; ORGANIC-MATTER; PARTICLE-SIZE; KINETICS; NANOSCALE; TOXICITY; MONOVALENT; MECHANISM; FIELD; ACID;
D O I
10.1021/es902987d
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
There is a pressing need for information on the mobility of nanoparticles in the complex aqueous matrices found in realistic environmental conditions. We dispersed three different metal oxide nanoparticles (TiO2, ZnO and CeO2) in samples taken from eight different aqueous media associated with seawater, lagoon, river, and groundwater, and measured their electrophoretic mobility, state of aggregation, and rate of sedimentation. The electrophoretic mobility of the particles in a given aqueous media was dominated by the presence of natural organic matter (NOM) and ionic strength, and independent of pH. NOM adsorbed onto these nanoparticles significantly reduces their aggregation, stabilizing them under many conditions. The transition from reaction to diffusion limited aggregation occurs at an electrophoretic mobility from around -2 to -0.8 mu m s(-1) V-1 cm. These results are key for designing and interpreting nanoparticle ecotoxicity studies in various environmental conditions.
引用
收藏
页码:1962 / 1967
页数:6
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