An experimental study of calcite dissolution rates at acidic conditions and 25 °C in the presence of NaPO3 and MgCl2

被引:59
作者
Alkattan, M [1 ]
Oelkers, EH [1 ]
Dandurand, JL [1 ]
Schott, J [1 ]
机构
[1] Univ Toulouse 3, CNRS, UMR 5563, OMP,Lab Geochim, F-31400 Toulouse, France
关键词
calcite dissolution rates; NaPO3; MgCl2;
D O I
10.1016/S0009-2541(02)00121-3
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
Dissolution rates of single calcite crystals were determined from sample weight loss using free-drift rotating disk techniques. Experiments were performed at 25 degreesC in aqueous HCl solutions over the bulk solution pH range - 1 to 3 and in the presence of trace concentrations of aqueous NaPO3 and MgCl2. These salts were chosen for this study because aqueous magnesium and phosphate are known to strongly inhibit calcite dissolution at neutral to basic pH. Reactive solutions were undersaturated with respect to possible secondary phases. Neither an inhibition or enhancement of calcite dissolution rates was observed in the presence of aqueous MgCl2 at pH 1 and 3. The presence of trace quantities of NaPO3, which dissociates in solution to Na+ and H2PO4-, decreased the overall calcite dissolution rate at pH less than or equal to 2. This contrasting behavior could be attributed to the different adsorption behavior of these dissolved species. As calcite surfaces are positively charged in acidic solutions, aqueous Mg2+ may not adsorb, whereas aqueous phosphate, present as either the anion H2PO4 or the neutral species H3PO40, readily adsorbs on calcite surfaces leading to significant dissolution inhibition. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:291 / 302
页数:12
相关论文
共 80 条
[1]   An experimental study of calcite and limestone dissolution rates as a function of pH from -1 to 3 and temperature from 25 to 80°C [J].
Alkattan, M ;
Oelkers, EH ;
Dandurand, JL ;
Schott, J .
CHEMICAL GEOLOGY, 1998, 151 (1-4) :199-214
[2]   Experimental studies of halite dissolution kinetics:: II.: The effect of the presence of aqueous trace anions and K3Fe(CN)6 [J].
Alkattan, M ;
Oelkers, EH ;
Dandurand, JL ;
Schott, J .
CHEMICAL GEOLOGY, 1997, 143 (1-2) :17-26
[3]  
ALKATTAN M, 1996, THESIS U P SABATIER
[4]  
ALKATTAN M, 1997, CHEM GEOL, V137, P210
[5]   KINETICS OF CALCITE DISSOLUTION AS AFFECTED BY CARBON-DIOXIDE PARTIAL-PRESSURE [J].
AMRHEIN, C ;
JURINAK, JJ ;
MOORE, WM .
SOIL SCIENCE SOCIETY OF AMERICA JOURNAL, 1985, 49 (06) :1393-1398
[6]  
[Anonymous], THESIS U P SABATIER
[7]  
[Anonymous], ACS S SER
[8]  
BATES RG, 1973, DETERMINATION PH
[9]   DISSOLUTION KINETICS OF CALCIUM-CARBONATE IN SEA-WATER .4. THEORY OF CALCITE DISSOLUTION [J].
BERNER, RA ;
MORSE, JW .
AMERICAN JOURNAL OF SCIENCE, 1974, 274 (02) :108-134
[10]   ROLE OF MAGNESIUM IN CRYSTAL-GROWTH OF CALCITE AND ARAGONITE FROM SEA-WATER [J].
BERNER, RA .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1975, 39 (04) :489-&