Mineral-water interfacial structures revealed by synchrotron X-ray scattering

被引:318
作者
Fenter, Paul [1 ]
Sturchio, Neil C. [2 ]
机构
[1] Argonne Natl Lab, Argonne, IL 60439 USA
[2] Univ Illinois, Dept Earth & Environm Sci, Chicago, IL 60607 USA
关键词
X-ray scattering; X-ray reflectivity; Crystal truncation rod; Water; Mineral-water interface; Solid-liquid interface; Interfacial water; Surface relaxation; Surface structure;
D O I
10.1016/j.progsurf.2004.12.001
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Chemical reactions occurring at the mineral-water interface are controlled by an interfacial layer, nanometers thick, whose properties may deviate from those of the respective bulk mineral and water phases. The molecular-scale structure of this interfacial layer, however, is poorly constrained, and correlations between macroscopic phenomena and molecular-scale processes remain speculative. The application of high-resolution X-ray scattering techniques has begun to provide substantial new insights into the molecular-scale structure of the mineral-water interface. In this review, we describe the characteristics of synchrotron-based X-ray scattering techniques that make them uniquely powerful probes of mineral-water interfacial structures and discuss the new insights that have been derived from their application. In particular, we focus on efforts to understand the structure and distribution of interfacial water as well as their dependence on substrate properties for major mineral classes including oxides, carbonates, sulfates, phosphates, silicates, halides and chromates. We compare these X-ray scattering results with those from other structural and spectroscopic techniques and integrate these to provide a conceptual framework upon which to base an understanding of the systematic variation of mineral-water interfacial structures. (C) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:171 / 258
页数:88
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