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氧化对纳米磁铁矿磁化的影响。

Effects of oxidation on the magnetization of nanoparticulate magnetite.

机构信息

Department of Civil and Environmental Engineering and The Institute of Critical Technology and Applied Science, NSF-EPA Center for the Environmental Implications of Nanotechnology, Virginia Tech, Blacksburg, Virginia 24060, USA.

出版信息

Langmuir. 2010 Nov 16;26(22):16745-53. doi: 10.1021/la102461z. Epub 2010 Sep 29.

Abstract

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(+)) 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(+) and Fe(II) caused a change in the magnetic properties of magnetite potentially because of alterations in its crystalline order. Magnetite oxidation caused a decrease in 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.

摘要

合成纳米磁铁矿已被提议作为一种潜在的反应剂,用于原位处理受污染的地下水。尽管磁铁矿纳米粒子在环境修复中的应用很有前景,但由于纳米粒子倾向于聚集并变得胶体不稳定,对颗粒反应性的全面了解受到了阻碍。颗粒之间的吸引力磁性相互作用部分是它们聚集的原因。在这项研究中,我们使用超导量子干涉装置 (SQUID) 来确定合成磁铁矿的饱和磁化强度、矫顽力、剩余磁化强度、磁化率和阻塞温度,从而对磁铁矿的磁性进行了表征。我们展示了这些特性在存在表面相关溶质(如四甲基铵 (TMA(+)) 和亚铁 (Fe(II)) 阳离子)时如何变化。更重要的是,因为磁铁矿很容易与 O(2)反应生成磁赤铁矿,所以我们分析了氧化对颗粒磁性的影响。由于磁赤铁矿的磁饱和报告值小于磁铁矿,我们假设氧化会降低相邻颗粒之间磁性吸引力的大小。TMA(+) 和 Fe(II) 的存在可能会改变其晶体有序性,从而改变磁铁矿的磁性。磁铁矿氧化导致饱和磁化强度降低,从而导致颗粒之间的磁性相互作用不那么显著。因此,氧化可能会导致磁铁矿纳米颗粒聚集减少,并潜在增强其胶体稳定性。

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