Will dawsonite form during CO2 storage?

被引:24
作者
Hellevang, Helge [1 ]
Aagaard, Per [2 ]
Jahren, Jens [1 ]
机构
[1] Univ Oslo, Dept Geosci, Oslo, Norway
[2] Univ Oslo, Oslo, Norway
关键词
Dawsonite; Nucleation; Growth; Rate; CLASTIC RESERVOIR ROCKS; DIAGENETIC ALBITIZATION; PRECIPITATION KINETICS; QUARTZ CEMENTATION; OFFSHORE NORWAY; BASIN; RATES; GEOCHEMISTRY; CONSTRAINTS; TEMPERATURE;
D O I
10.1002/ghg.1378
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
For more than a decade, a debate has been going on as to whether dawsonite can sequester CO2, and be the dominant secondary carbonate where reservoirs lack divalent metal cations. Numerical simulations have suggested large-scale formation, whereas natural occurrences in present-day or previously CO2-charged reservoirs are scarce. Natural occurrences, such as in sequences of the Hailaer and Songliao basins, may nevertheless suggest that dawsonite can form under CO2 storage conditions (<120 degrees C) given the right temperature-composition window. The exact conditions, however (CO2 pressure, alkalinity, temperature, ionic strength) are highly uncertain. Moreover, there are no data on the rate of nucleation and growth of dawsonite, and numerical predictions are forced into using simplified kinetic expressions with values of kinetic constants obtained from far-from-equilibrium dissolution rate experiments, a method that is questioned today. There are good indications that a range of reservoirs may become supersaturated with respect to dawsonite during CO2 storage, but this does not imply spontaneous growth. The retention time (the nucleation stage) may be long, and growth rates may be significantly lower than predicted from the far-from-equilibrium dissolution rates. The lack of nucleation and growth rate data for dawsonite, the lack of dawsonite growth in laboratory experiments under CO2 storage conditions (not highly alkaline), and the uncertainty in growth conditions for the natural analogues, thus render numerical predictions highly uncertain. Conclusions on the mineral carbonatization potential should therefore be taken with caution if dawsonite is the dominant secondary carbonate predicted to form. (c) 2013 Society of Chemical Industry and John Wiley & Sons, Ltd
引用
收藏
页码:191 / 199
页数:9
相关论文
共 45 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]   DIAGENETIC ALBITIZATION OF DETRITAL K-FELDSPARS IN JURASSIC, LOWER CRETACEOUS AND TERTIARY CLASTIC RESERVOIR ROCKS FROM OFFSHORE NORWAY, .2. FORMATION WATER CHEMISTRY AND KINETIC CONSIDERATIONS [J].
AAGAARD, P ;
EGEBERG, PK ;
SAIGAL, GC ;
MORAD, S ;
BJORLYKKE, K .
JOURNAL OF SEDIMENTARY PETROLOGY, 1990, 60 (04) :575-581
[3]  
[Anonymous], 2007, DEV GEOCHEM
[4]  
[Anonymous], 1979, ACS SYM SER
[5]   Tentative Kinetic Model for Dolomite Precipitation Rate and Its Application to Dolomite Distribution [J].
Arvidson, Rolf S. ;
Mackenzie, Fred T. .
AQUATIC GEOCHEMISTRY, 1996, 2 (03) :273-298
[6]   The dolomite problem: Control of precipitation kinetics by temperature and saturation state [J].
Arvidson, RS ;
Mackenzie, FT .
AMERICAN JOURNAL OF SCIENCE, 1999, 299 (04) :257-288
[7]   Two-dimensional reactive transport modeling of CO2 injection in a saline Aquifer at the Sleipner site, North Sea [J].
Audigane, Pascal ;
Gaus, Irina ;
Czernichowski-Lauriol, Isabelle ;
Pruess, Karsten ;
Xu, Tianfu .
AMERICAN JOURNAL OF SCIENCE, 2007, 307 (07) :974-1008
[8]  
BAKER JC, 1995, J SEDIMENT RES A, V65, P522
[9]   Dawsonite synthesis and reevaluation of its thermodynamic properties from solubility measurements:: Implications for mineral trapping of CO2 [J].
Benezeth, Pascale ;
Palmer, Donald A. ;
Anovitz, Lawrence M. ;
Horita, Juske .
GEOCHIMICA ET COSMOCHIMICA ACTA, 2007, 71 (18) :4438-4455
[10]   CO2 Sequestration in Deep Sedimentary Formations [J].
Benson, Sally M. ;
Cole, David R. .
ELEMENTS, 2008, 4 (05) :325-331