An experimental study of dolomite dissolution kinetics at conditions relevant to CO2 geological storage

被引:2
作者
Baritantonaki, Angeliki [1 ]
Bolourinejad, Panteha [1 ,2 ]
Herber, Rien [1 ]
机构
[1] Univ Groningen, Dept Geoenergy, Nijenborgh 4, NL-9747AG Groningen, Netherlands
[2] NAM, Schepersmaat 2, NL-9405 TA Assen, Netherlands
关键词
REACTIVE SURFACE-AREA; CALCITE DISSOLUTION; ACTIVATED COMPLEX; AQUEOUS-SOLUTIONS; PH; SEQUESTRATION; RATES; 25-DEGREES-C; TEMPERATURE; CONSTRAINTS;
D O I
10.1144/petgeo2016-048
中图分类号
P [天文学、地球科学];
学科分类号
07 ;
摘要
The kinetics of dolomite dissolution have been experimentally investigated under subsurface conditions characteristic of the Rotliegend gas fields in the NE of The Netherlands. Experiments were performed in closed, stirred, batch reactors at far from equilibrium conditions, with dolomite powders of different grain sizes. The experiments were repeated for all grain sizes at 25 degrees C and an experiment was also conducted in deionized water. The rates were derived from the measured concentrations of Mg2+ or Ca2+ released from dolomite dissolution and were normalized by the surface area of the minerals at each time interval. Regression of the rates with the pH resulted in the kinetic rate constants of: log k(1) = -8.16 +/- 0.06 at 25 degrees C and log k(2) = -7.61 +/- 0.05 at 100 degrees C (300 - 350 mu m), log k(3) = -7.88 +/- 0.20 at 25 degrees C, log k(4) = -7.45 at 100 degrees C (75 - 100 mu m), log k(5) = -6.62 +/- 0.50 at 25 degrees C and log k(6) = -5.96 +/- 1 at 100 degrees C (20 - 25 mu m). The results obtained in this study indicate that in an acidic regime the dissolution of dolomite in brine is a factor of 2 faster than in deionized water. It was also shown that the dissolution rates, when normalized by surface area, increase with decreasing grain size.
引用
收藏
页码:353 / 362
页数:10
相关论文
共 48 条
[1]   THERMODYNAMIC AND KINETIC CONSTRAINTS ON REACTION-RATES AMONG MINERALS AND AQUEOUS-SOLUTIONS .1. THEORETICAL CONSIDERATIONS [J].
AAGAARD, P ;
HELGESON, HC .
AMERICAN JOURNAL OF SCIENCE, 1982, 282 (03) :237-285
[2]   IONIC CONCENTRATIONS AND ACTIVITIES IN SOIL SOLUTIONS [J].
ADAMS, F .
SOIL SCIENCE SOCIETY OF AMERICA PROCEEDINGS, 1971, 35 (03) :420-&
[3]   Sequestering CO2 by Mineral Carbonation: Stability against Acid Rain Exposure [J].
Allen, Daniel J. ;
Brent, Geoff F. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2010, 44 (07) :2735-2739
[4]  
[Anonymous], 2015, The Paris Agreement
[5]  
[Anonymous], 2001, CLIMATE CHANGE 2001
[6]  
[Anonymous], CONTRIBUTION WORKING
[7]   Sequestration of CO2 in geological media in response to climate change:: capacity of deep saline aquifers to sequester CO2 in solution [J].
Bachu, S ;
Adams, JJ .
ENERGY CONVERSION AND MANAGEMENT, 2003, 44 (20) :3151-3175
[8]   AQUIFER DISPOSAL OF CO2 - HYDRODYNAMIC AND MINERAL TRAPPING [J].
BACHU, S ;
GUNTER, WD ;
PERKINS, EH .
ENERGY CONVERSION AND MANAGEMENT, 1994, 35 (04) :269-279
[9]  
Barrante J.R., 1974, APPL MATH PHYS CHEM
[10]  
Bibi I., 2010, Proceedings of the 19th World Congress of Soil Science: Soil solutions for a changing world, Brisbane, Australia, 1-6 August 2010. Working Group 3.1 Processes in acid sulfate soil materials, P36