首页 | 本学科首页   官方微博 | 高级检索  
     检索      

Gneiss-Water Interaction and Water Evolution During the Early Stages of Dissolution Experiments at Room Temperature
作者姓名:朱义年
作者单位:[1]Dept.ofResourceandEnvironmentalEngineering,GuilinInstituteofTechnology,Guilin541004,China [2]GeologicalSurvey,Baden-Wuirttemberg,Albertstr.5,79104Freiburg,Germany [3]InstituteforMineralogy,PetrologyandGeochemistry,UniversityofFreiburg,Albertstr.23b,79104Freiburg,Germany
基金项目:FinancialsupportbyDAAD (GermanAcademicExchangeService)andtheSachtlebenBergbauGmbHisgratefullyacknowledged.
摘    要:Gneiss-distilled water interaction at room temperature was investigated with batch-reactors to study water-rock reaction and geochemical evolution of the aqueous phase with time. The ion concentrations in water were controlled not only by the dissolution of primary minerals, but also by the precipitation of secondary minerals. The decreasing fraction sizes of gneiss could favor dissolution and precipitation simultaneously. Ca^2 and K^ were the major cations, and HCO3^- was the major anion in water. All the ions except Ca^2 increased in concentration with time. The Ca^2 release from the rock to the aqueous phase was initially much faster than the release of K^ , Na^2 and Mg^2 . But after about 5 - 24 hours, the Ca^2 concentrations in water decreased very slowly with time and became relatively stable. During the experiment, the water varied from the Ca-( K)-HCO3-type water to the K-Ca-HCO3-type water, and then to the K-(Ca, Na)-HCO3-type water. The water-gneiss interaction was dominated by the dissolution of Kfeldspar in the solution. The remaining secondary minerals were mainly kaolinite, illite and K (Mg) -mica.

关 键 词:gneLss  water  interaction  water  evolufion
收稿时间:29 February 2008

Gneiss-Water interaction and water evolution during the early stages of dissolution experiments at room temperature
Zhu Yinian,Ingrid Stober,Kurt Bucher.Gneiss-Water Interaction and Water Evolution During the Early Stages of Dissolution Experiments at Room Temperature[J].Chinese Journal of Geochemistry,2003,22(4):302-312.
Authors:Zhu Yinian  Ingrid Stober  Kurt Bucher
Institution:(1) Dept. of Resource and Environmental Engineering, Cuilin Institute of Technology, 541004 Guilin, China;(2) Institute for Mineralogy, Petrology and Geochemistry, University of Freiburg, Albertstr. 23b, 79104 Freiburg, Germany;(3) Geological Survey, Baden-Württemberg, Albertstr. 5, 79104 Freiburg, Germany
Abstract:Gneiss\|distilled water interaction at room temperature was investigated with batch\|reactors to study water\|rock reaction and geochemical evolution of the aqueous phase with time. The ion concentrations in water were controlled not only by the dissolution of primary minerals, but also by the precipitation of secondary minerals. The decreasing fraction sizes of gneiss could favor dissolution and precipitation simultaneously. Ca\+\{2+\} and K\++ were the major cations, and HCO\+-\-3 was the major anion in water. All the ions except Ca\+\{2+\} increased in concentration with time. The Ca\+\{2+\} release from the rock to the aqueous phase was initially much faster than the release of K\++, Na\++ and Mg\+\{2+\}. But after about 5-24 hours, the Ca\+\{2+\} concentrations in water decreased very slowly with time and became relatively stable. During the experiment, the water varied from the Ca\|(K)\|HCO\-3\|type water to the K\|Ca\|HCO\-3\|type water, and then to the K\|(Ca,Na)\|HCO\-3\|type water. The water\|gneiss interaction was dominated by the dissolution of K\|feldspar in the solution. The remaining secondary minerals were mainly kaolinite, illite and K(Mg)\|mica.
Keywords:gneiss  water  interaction  water evolution
本文献已被 CNKI 维普 万方数据 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号