DISSOLUTION OF PRIMARY BASALTIC MINERALS IN NATURAL-WATERS - SATURATION STATE AND KINETICS

被引:123
作者
GISLASON, SR
ARNORSSON, S
机构
[1] Science Institute, University of Iceland, Reykjavik, Dunhagi 3
关键词
D O I
10.1016/0009-2541(93)90122-Y
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
The state of saturation of olivine, orthopyroxene and plagioclase of variable composition has been assessed in various types of natural waters in Iceland including river waters, groundwater and geothermal waters with temperatures up to 250-degrees-C. The stability of olivine and orthopyroxene decreases with increasing Mg content. Similarly, the stability of plagioclase decreases with increasing anorthite content. The river waters which are representative of the weathering environment are always undersaturated with both olivine and orthopyroxene, the degree of undersaturation being dominated by the water pH. All river waters tend to dissolve olivine of the composition encountered in basalts according to the linear rate law and orthopyroxene when the pH is < 8. Groundwaters, which have a higher pH, appear to dissolve orthopyroxene and Fe-rich olivine according to the slower near-equilibrium dissolution rate law. In river waters and groundwaters Na-rich plagioclase is stable but when Ca-rich it is close to equilibrium or slightly undersaturated. The state of saturation is independent of pH in the range occurring in these waters (pH 7-10). Geothermal waters of high temperature ( > 200-degrees-C) are undersaturated with olivine, orthopyroxene and plagioclase, the first two particularly when Fe rich, and sufficient to cause olivine to dissolve according to the linear rate law. At intermediate temperatures (50-150-degrees-C) the geothermal waters are close to equilibrium with these minerals except for Mg-rich olivine. It seems likely that dissolution of glass from basalt, which is very reactive, will favor stability of the igneous minerals.
引用
收藏
页码:117 / 135
页数:19
相关论文
共 65 条
[1]  
APPS JA, 1988, NUREGCR5271 US NUCL
[2]   THE CHEMISTRY OF GEOTHERMAL WATERS IN ICELAND .3. CHEMICAL GEOTHERMOMETRY IN GEOTHERMAL INVESTIGATIONS [J].
ARNORSSON, S ;
GUNNLAUGSSON, E ;
SVAVARSSON, H .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1983, 47 (03) :567-577
[3]   THE CHEMISTRY OF GEOTHERMAL WATERS IN ICELAND .1. CALCULATION OF AQUEOUS SPECIATION FROM O-DEGREE-C TO 370-DEGREE-C [J].
ARNORSSON, S ;
SIGURDSSON, S ;
SVAVARSSON, H .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1982, 46 (09) :1513-1532
[4]   CHEMISTRY OF GASES ASSOCIATED WITH GEOTHERMAL ACTIVITY AND VOLCANISM IN ICELAND - A REVIEW [J].
ARNORSSON, S .
JOURNAL OF GEOPHYSICAL RESEARCH-SOLID EARTH AND PLANETS, 1986, 91 (B12) :2261-2268
[5]   THE CHEMISTRY OF GEOTHERMAL WATERS IN ICELAND .2. MINERAL EQUILIBRIA AND INDEPENDENT VARIABLES CONTROLLING WATER COMPOSITIONS [J].
ARNORSSON, S ;
GUNNLAUGSSON, E ;
SVAVARSSON, H .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1983, 47 (03) :547-566
[6]   NEW GAS GEOTHERMOMETERS FOR GEOTHERMAL-EXPLORATION - CALIBRATION AND APPLICATION [J].
ARNORSSON, S ;
GUNNLAUGSSON, E .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1985, 49 (06) :1307-1325
[7]   INTERNALLY-CONSISTENT THERMODYNAMIC DATA FOR MINERALS IN THE SYSTEM NA2O-K2O-CAO-MGO-FEO-FE2O3-AL2O3-SIO2-TIO2-H2O-CO2 [J].
BERMAN, RG .
JOURNAL OF PETROLOGY, 1988, 29 (02) :445-522
[8]  
BOURCIER WL, 1993, UNPUB ALUMINUM HYDRO
[9]   FREE-ENERGY DEPENDENCE OF ALBITE DISSOLUTION KINETICS AT 80-DEGREES-C AND PH 8.8 [J].
BURCH, TE ;
NAGY, KL ;
LASAGA, AC .
CHEMICAL GEOLOGY, 1993, 105 (1-3) :137-162
[10]  
BURCH TE, 1991, 1991 GEOL SOC AM ANN, pA260