Incongruent dissolution of wollastonite measured with vertical scanning interferometry

被引:30
作者
Green, E [1 ]
Luttge, A
机构
[1] Univ Calif Berkeley, Dept Earth & Planetary Sci, Berkeley, CA 94709 USA
[2] Rice Univ, Dept Earth Sci, Houston, TX 77005 USA
[3] Rice Univ, Dept Chem, Houston, TX 77005 USA
关键词
wollastonite; dissolution kinetics; leached layer; interferometry; mineral dissolution; surface studies;
D O I
10.2138/am.2006.1968
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
In this Study, we investigated the dissolution kinetics of wollastonite, a pyroxenoid with composition CaSiO3, at earth-surface temperatures. We used vertical scanning interferometry (VSI) to quantify the surface normal retreat (or advance) of it crystallographically defined cleavage face on a single wollastonite crystal its it function of time. Nanometer-scale measurements of (100) faces show that the wollastonite surface undergoes a net expansion normal to the surface and relative to the pristine mineral surface. These observations were made during the dissolution process at acidic conditions. The swelling is the result of the Formation of a cation-depleted layer at the wollastonite-water interface. We combined VSI measurements with electron microprobe measurements to track the chemical evolution of the leached layer during dissolution, and then used previously reported Ca release rates to calculate the density of the cation-depleted layer. Using ail average Ca release of 9.09 x 10(-9) mol/m(2-)s at pH 3 and 25 degrees C, the density of the leached layer is 1.2 g/cm(3), and grows to a thickness of similar to 50 nm after 20 hours of reaction. Although our observations do show direct evidence of the formation of a cation-depleted layer during dissolution, they do not favor a particular mechanism of formation of this layer. At this time, Our results cannot rule out either cation migration through the depleted crystal Structure or re-precipitation at the mineral surface.
引用
收藏
页码:430 / 434
页数:5
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