Experimental Determination of Calcite Dissolution Rates and Equilibrium Concentrations in Deionized Water Approaching Calcite Equilibrium

被引:0
作者
龚庆杰
邓军
王庆飞
杨立强
佘敏
机构
[1] StateKeyLaboratoryofGeologicalProcessesandMineralResources,ChinaUniversityofGeosciences
关键词
calcite; dissolution rate; equilibrium concentration; reaction order;
D O I
暂无
中图分类号
P579 [实验矿物学、应用矿物学];
学科分类号
070901 ;
摘要
The calcite dissolution rates at 50-250 ℃ and 20 MPa in deionized water with flow rate varying from 0.2 to 5 mL/min were experimentally measured in a continuous flow column pressure vessel reactor.Equilibrium concentration(ceq) of calcite dissolution in deionized water at 20 MPa was determined using dissolution data according to the iterative method presented by Jeschke and Dreybrodt.The equilibrium concentrations at 50,100,150,200 and 250 ℃ are 1.84×10-4,2.23×10-4,2.25×10-4,2.31×10-4 and 2.24×10-4 mol/L,respectively.The ceq increases first and then decreases with temperature varying from 50 to 250 ℃ at 20 MPa,and the same variation trend occurs at 10 MPa with lower values.The maximum value(or extremum) of ceq would increase with temperature at constant pressures.The dissolution reaction of calcite in this experiment is approaching the calcite equilibrium,and the reaction order doesn't keep a constant at different temperatures,which could imply that a change of the reaction mechanism was occurring.The Arrhenius equation shouldn't be used to calculate apparent activation energy using rate constant data at different temperatures when the reaction order or reaction mechanism changed.
引用
收藏
页码:402 / 411
页数:10
相关论文
共 15 条
[1]   Mechanism of Secondary Pore Formation and Prediction of Favorable Reservoir of Paleogene in Jiyang Sag, Eastern China [J].
朱筱敏 ;
陈欢庆 ;
钟大康 ;
张琴 ;
张善文 ;
吕希学 .
Journal of China University of Geosciences, 2008, 19 (06) :675-684
[2]  
Calcite Dissolution in Deionized Water from 50℃ to 250℃ at 10 MPa:Rate Equation and Reaction Order[J]. GONG Qingjie~* DENG Jun WANG Qingfei YANG Liqiang SHE Min State Key Laboratory of Geological Processes and Mineral Resources,China University of Geosciences,Beijing 100083.Acta Geologica Sinica(English Edition). 2008(05)
[3]  
Mechanism for calcite dissolution and its contribution to development of reservoir porosity and permeability in the Kela 2 gas field,Tarim Basin,China[J]. YU BingSong1,3, DONG HailLiang2,3 & RUAN Zhuang1,3 1 State Key Laboratory of Geological Processes and Mineral Resources, China University of Geosciences, Beijing 100083, China;2 Department of Geology, Miami University,Oxford, OH 45056, USA;3 Geomicrobiology Laboratory, China University of Geosciences, Beijing, 100083, China.Science in China(Se
[4]  
Carbonate Diagenesis Controlled by Glacioeustatic Sea-Level Changes: A Case Study from the Carboniferous-Permian Boundary Section at Xikou, China[J]. 张海军,丁林,王训练,王雷,王清山,夏国英.Journal of China University of Geosciences. 2006(02)
[5]  
Calcite dissolution kinetics in the system CaCO 3 –H 2 O–CO 2 at high undersaturation[J] . Georg Kaufmann,Wolfgang Dreybrodt.Geochimica et Cosmochimica Acta . 2007 (6)
[6]  
Calcite dissolution kinetics in Na–Ca–Mg–Cl brines[J] . Dwight K. Gledhill,John W. Morse.Geochimica et Cosmochimica Acta . 2006 (23)
[7]   Comparative study of dissolution rate-determining mechanisms of limestone and dolomite [J].
Liu, ZH ;
Yuan, DX ;
Dreybrodt, W .
ENVIRONMENTAL GEOLOGY, 2005, 49 (02) :274-279
[8]   How do mineral coatings affect dissolution rates?: An experimental study of coupled CaCO3 dissolution -: CdCO3 precipitation [J].
Cubillas, P ;
Köhler, S ;
Prieto, M ;
Causserand, C ;
Oelkers, EH .
GEOCHIMICA ET COSMOCHIMICA ACTA, 2005, 69 (23) :5459-5476
[9]  
The processes dominating Ca dissolution of limestone when exposed to ambient atmospheric conditions as determined by comparing dissolution models[J] . C. Cardell-Fernández,G. Vleugels,K. Torfs,R. Van Grieken.Environmental Geology . 2002 (1-2)
[10]  
The dissolution kinetics of major sedimentary carbonate minerals[J] . John W Morse,Rolf S Arvidson.Earth Science Reviews . 2002 (1)