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锶在水合氧化锰上吸附的局部结构分析

Local Structure Analysis of Strontium Sorption to Hydrous Manganese Oxide.

作者信息

Axe L, Tyson T, Trivedi P, Morrison T

机构信息

Department of Civil and Environmental Engineering, New Jersey Institute of Technology, Newark, New Jersey, 07102

出版信息

J Colloid Interface Sci. 2000 Apr 15;224(2):408-416. doi: 10.1006/jcis.2000.6737.

Abstract

To develop mechanistic models of contaminant distribution processes, we conducted an X-ray absorption fine structure analysis of strontium sorption to hydrous manganese oxide (HMO). Sr K-edge measurements were performed at 298, 220, and 77 K, and at sample loadings from 10(-4) to 10(-2) mol Sr/g HMO. Results from fitting the first shell in the sorbed samples indicate that strontium is surrounded by 10-12 oxygen atoms at an average distance of 2.58 Å. This coordination environment is consistent with the strontium atom remaining hydrated upon sorption to the oxide, where in water hydrated strontium has approximately 9 atoms of oxygen at 2.62 Å. Furthermore, the temperature dependence of the strontium-oxygen bond also suggests physical adsorption due to the large contribution of the dynamic component of the Debye Waller factor. Although second-shell data are consistent with either 3 manganese atoms at 4.12 Å or 6 strontium atoms at 3.88 Å, both the near-edge and fine structure data for the manganese K-edge indicate that the local coordination environment of the manganese ion remains intact as a function of time or strontium sorption. Furthermore, the local structure of amorphous manganese oxide is highly ordered. Copyright 2000 Academic Press.

摘要

为了建立污染物分布过程的机理模型,我们对锶在水合氧化锰(HMO)上的吸附进行了X射线吸收精细结构分析。在298K、220K和77K以及样品负载量为10^(-4)至10^(-2) mol Sr/g HMO的条件下进行了Sr K边测量。对吸附样品中第一壳层拟合的结果表明,锶被10 - 12个氧原子包围,平均距离为2.58 Å。这种配位环境与锶在吸附到氧化物上时仍保持水合状态一致,在水中水合锶在2.62 Å处大约有9个氧原子。此外,锶 - 氧键的温度依赖性也表明是物理吸附,这是由于德拜 - 瓦勒因子的动态成分贡献很大。虽然第二壳层数据与4.12 Å处的3个锰原子或3.88 Å处的6个锶原子一致,但锰K边的近边和精细结构数据均表明,锰离子的局部配位环境随时间或锶吸附而保持不变。此外,非晶态氧化锰的局部结构高度有序。版权所有2000年学术出版社。

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