Magnesite growth rates as a function of temperature and saturation state

被引:223
作者
Saldi, Giuseppe D. [1 ]
Jordan, Guntram [2 ]
Schott, Jacques [1 ]
Oelkers, Eric H. [1 ]
机构
[1] Univ Toulouse, LMTG CNRS OMP, F-31400 Toulouse, France
[2] Univ Munich, Dept Geo & Umweltwissensch, D-80333 Munich, Germany
关键词
ATOMIC-FORCE MICROSCOPY; SCANNING PROBE MICROSCOPY; ACIDIC AQUEOUS-SOLUTION; IN-SITU AFM; CRYSTAL-GROWTH; MOLECULAR-SCALE; CALCITE GROWTH; CARBON-DIOXIDE; ELECTROLYTE-SOLUTIONS; DISSOLUTION KINETICS;
D O I
10.1016/j.gca.2009.06.035
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
Magnesite growth rates and step velocities have been measured systematically as a function of temperature from 80 to 105 degrees C and saturation state in 0.1 M NaCl solutions using hydrothermal atomic force microscopy (HAFM). The observations indicate that at these conditions magnesite precipitation is dominated by the coupling of step generation via spiral growth at screw dislocations and step advancement away from these dislocations. As these two processes occur in series the slowest of these dominates precipitation rates. At 100 degrees C magnesite growth rates (r) determined by HAFM are consistent with r = k(Omega - 1)(2), where k is a constant equal to 6.5 x 10(-16) mol/cm(2)/s and Omega is the saturation index with respect to magnesite. This equation is consistent with spiral growth step generation controlling magnesite precipitation rates. Corresponding magnesite precipitation rates measured using mixed-flow reactors are shown to be consistent with both the rates measured by HAFM and the spiral growth theory, confirming the rate limiting mechanism. Step advancement, however, is observed to slow far faster than step generation with decreasing temperature; the activation energy for step advancement is 159 kJ/mol whereas step generation rates have an estimated activation energy of similar to 60 kJ/mol. As such, it seems likely that at ambient temperatures magnesite growth is limited by very slow step advancement rates. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5646 / 5657
页数:12
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