An EFTEM/HRTEM high-resolution study of the near surface of labradorite feldspar altered at acid pH: evidence for interfacial dissolution-reprecipitation

被引:165
作者
Hellmann, R [1 ]
Penisson, JM
Hervig, RL
Thomassin, JH
Abrioux, MF
机构
[1] Univ Grenoble 1, OSUG, LGIT, CNRS,UMR C5559, F-38041 Grenoble 9, France
[2] CEA Grenoble, DRFMC, F-38054 Grenoble, France
[3] Arizona State Univ, Ctr Solid State Sci, Tempe, AZ 85287 USA
[4] Univ Poitiers, ESIP, LMGE, CNRS,UMR 6532, F-86022 Poitiers, France
关键词
feldspar dissolution; EFTEM and HRTEM; interfacial dissolution; reprecipitation mechanism; leached layers and preferential cation release;
D O I
10.1007/s00269-003-0308-4
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Using an approach combining high-resolution and energy-filtered transmission electron microscopy (HRTEM and EFTEM), we have studied with Angstrom to nm-spatial resolution the interfacial region that delimits the near-surface altered zone and non-altered labradorite feldspar after dissolution under acid pH conditions. The interface is characterized by extremely sharp and spatially coincident changes in structure and chemistry. The 500-nm-thick altered zone is depleted in interstitial cations (Ca, Na, K) and Al, a framework element, whereas it is enriched in H, O, and Si. Modeling H+-alkali interdiffusion within a 500-nm-thick altered zone shows that volume interdiffusion cannot reproduce the sharp chemical interfaces measured by EFTEM. Based on these new data, we propose that the near-surface altered zone is a result of interfacial dissolution-reprecipitation, and not of preferential leaching of cations and interdiffusion with H+. This implies an intrinsic dissolution process that is stoichiometric, where the breaking of bonds and release of interstitial cations and framework elements (Al, Si, and O) to solution occur contemporaneously at equal relative rates from the original fluid mineral interface.
引用
收藏
页码:192 / 197
页数:6
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