An atomic force microscopy study of calcite dissolution in saline solutions: The role of magnesium ions

被引:102
|
作者
Ruiz-Agudo, E. [1 ]
Putnis, C. V. [2 ]
Jimenez-Lopez, C. [3 ]
Rodriguez-Navarro, C. [1 ]
机构
[1] Univ Granada, Dept Mineral & Petrol, Granada 18002, Spain
[2] Univ Munster, Inst Mineral, D-48149 Munster, Germany
[3] Univ Granada, Dept Microbiol, Granada 18002, Spain
关键词
CARBONATE MINERALS; AQUEOUS-SOLUTION; KINETICS; SURFACE; GROWTH; RATES; INHIBITION; WATER; MG2+; SOLUBILITY;
D O I
10.1016/j.gca.2009.03.016
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 situ Atomic Force Microscopy, AFM, experiments have been carried Out using calcite cleavage surfaces in contact with solutions of MgSO4, MgCl2, Na2SO4 and NaCl in order to attempt to understand the role of Mg2+ during calcite dissolution. Although previous work has indicated that magnesium inhibits calcite dissolution, quantitative AFM analyses show that despite the fact that Mg2+ inhibits etch pit spreading, it increases the density and depth of etch pits nucleated oil calcite surfaces and, subsequently, the overall dissolution rates: i.e., froin 10(-11.75) mol cm(-2) s(-1) (in deionized water) up to 10(-10.54) mol cm(-2) s(-1) (in 2.8 M MgSO4). Such an effect is concentration-clepenclent and it is most evident in concentrated solutions ([Mg2+] >> 50 mM). These results show that common soluble salts (especially Mg sulfates) may play it critical role in the chemical weathering of carbonate rocks in nature its well as in the decay of carbonate stone in buildings and statuary. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3201 / 3217
页数:17
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