Effects of Oxidation on the Magnetization of Nanoparticulate Magnetite

被引:147
作者
Rebodos, Robert L.
Vikesland, Peter J. [1 ]
机构
[1] Virginia Tech, NSF EPA Ctr Environm Implicat Nanotechnol CEINT, Dept Civil & Environm Engn, Blacksburg, VA 24060 USA
基金
美国国家科学基金会;
关键词
IRON-OXIDE NANOPARTICLES; PARTICLE-SIZE; AGGREGATION; DISPERSIONS; KINETICS; SEDIMENTATION; FLOCCULATION; REDUCTION; FILMS;
D O I
10.1021/la102461z
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Synthetic nanomagnetite has been suggested as a potential reactant for the in situ treatment of contaminated groundwater. Although the application of magnetite nanoparticles for environmental remediation is promising, a full understanding of particle reactivity has been deterred by the propensity of the nanoparticles to aggregate and become colloidally unstable, Attractive magnetic interactions between particles are partially responsible for their aggregation. In this study, we characterized the magnetic behavior of magnetite by determining the saturation magnetization, coercivity, remanent magnetization, susceptibility, and blocking temperature of synthetic magnetite using a superconducting quantum interference device (SQUID). We show how these properties vary in the presence of surface-associated solutes such as tetramethylammonium (TMA(1)) and ferrous (Fe-II) cations. More importantly, because magnetite readily reacts with O-2 to produce maghemite, we analyzed the effect of oxidation on the magnetic properties of the particles. Because maghemite has a reported magnetic saturation that is less than that of magnetite, we hypothesized that oxidation would decrease the magnitude of the magnetic attractive force between adjacent particles. The presence of TMA(4) and Fe-II caused si change in the magnetic properties of magnetite potentially because of alterations in its crystalline order. Magnetite oxidation caused a decrease M saturation magnetization, resulting in less significant magnetic interactions between particles. Oxidation, therefore, could lead to the decreased aggregation of magnetite nanoparticles and a potential enhancement of their colloidal stability.
引用
收藏
页码:16745 / 16753
页数:9
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