Dynamics of fossil fuel CO2 neutralization by marine CaCO3

被引:200
|
作者
Archer, D
Kheshgi, H
Maier-Reimer, E
机构
[1] Univ Chicago, Dept Geophys Sci, Chicago, IL 60637 USA
[2] ExxonMobil Res & Engn Co, Annandale, NJ 08801 USA
[3] Max Planck Inst Meteorol, D-20146 Hamburg 54, Germany
关键词
D O I
10.1029/98GB00744
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A detailed model of the ocean circulation and carbon cycle was coupled to a mechanistic model of CaCO3 diagenesis in deep sea sediments to simulate the millennium-scale response of the oceans to future fossil fuel CO2 emissions to the atmosphere and deep sea. Simulations of deep sea injection of CO2 show that CaCO3 dissolution is sensitive to passage of high-CO2 waters through the Atlantic Ocean, but CaCO3 dissolution has a negligible impact on atmospheric pCO(2) or the atmospheric stabilization CO2 emission in the coming centuries. The ultimate fate of the fossil fuel CO2 will be to react with CaCO3 on the seafloor and on land. An initial CaCO3 dissolution spike reverses the net sedimentation rate in the ocean until it is attenuated by an enhanced vertical gradient of alkalinity after about 1000 years. The magnitude of the initial spike is sensitive to assumptions about the kinetics for CaCO3 dissolution, but subsequent behavior appears to be less model dependent. Neutralization by seafloor CaCO3 occurs on a timescale of 5-6 kyr, and is limited to at most 60-70% of the fossil fuel release, even if the fossil fuel release is smaller than the seafloor erodible inventory of CaCO3. Additional neutralization by terrestrial CaCO3 restores a balance between CaCO3 weathering and seafloor accumulation on a timescale of 8.5 kyr, while the deficit of seafloor CaCO3 (the lysocline) is replenished with an e-folding timescale of approximately 18 kyr. The final equilibrium with CaCO3 leaves 7-8% of the fossil fuel CO2 remaining in the atmosphere, to be neutralized by the silicate rock cycle on a time frame of hundreds of thousands of years.
引用
收藏
页码:259 / 276
页数:18
相关论文
共 50 条
  • [1] Multiple timescales for neutralization of fossil fuel CO2
    Archer, D
    Kheshgi, H
    MaierReimer, E
    GEOPHYSICAL RESEARCH LETTERS, 1997, 24 (04) : 405 - 408
  • [2] Decomposition kinetics of CaCO3 in CO2 atmosphere
    Zheng, Ying
    Song, Kan
    Chi, Baohua
    Zheng, Chuguang
    Huazhong Keji Daxue Xuebao (Ziran Kexue Ban)/Journal of Huazhong University of Science and Technology (Natural Science Edition), 2007, 35 (08): : 87 - 89
  • [3] Energy analysis of CaCO3 calcination with CO2 capture
    Lin, Shiying
    Kiga, Takashi
    Wang, Yin
    Nakayama, Katsuhiro
    10TH INTERNATIONAL CONFERENCE ON GREENHOUSE GAS CONTROL TECHNOLOGIES, 2011, 4 : 356 - 361
  • [4] Impact of anthropogenic CO2 on the CaCO3 system in the oceans
    Feely, RA
    Sabine, CL
    Lee, K
    Berelson, W
    Kleypas, J
    Fabry, VJ
    Millero, FJ
    SCIENCE, 2004, 305 (5682) : 362 - 366
  • [5] Current CaCO3 dissolution at the seafloor caused by anthropogenic CO2
    Sulpis, Olivier
    Boudreau, Bernard P.
    Mucci, Alfonso
    Jenkins, Chris
    Trossman, David S.
    Arbic, Brian K.
    Key, Robert M.
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2018, 115 (46) : 11700 - 11705
  • [6] The Role of CaCO3 Reactions in the Contemporary Oceanic CO2 Cycle
    Smith, Stephen V.
    Mackenzie, Fred T.
    AQUATIC GEOCHEMISTRY, 2016, 22 (02) : 153 - 175
  • [7] The Role of CaCO3 Reactions in the Contemporary Oceanic CO2 Cycle
    Stephen V. Smith
    Fred T. Mackenzie
    Aquatic Geochemistry, 2016, 22 : 153 - 175
  • [8] Application of CaCO3 activated by CO2 in semidry FGD process
    School of Municipal and Environmental Engineering, Shenyang Jianzhu University, Shenyang 110168, China
    不详
    Shenyang Jianzhu Daxe Xuebao, 2006, 2 (277-280):
  • [9] Direct sulfation of CaCO3: the influence of CO2 partial pressure
    Nyman, Gunnar
    Ghardashkhani, Sohbat
    Energy and Fuels, 1993, 7 (04): : 512 - 519
  • [10] EFFECT OF CACO3 CONTENT ON THE DEGREE OF CO2 CURING OF CONCRETE
    Tu, Zhenjun
    Shi, Caijun
    He, Pingping
    Cao, Zhang
    ADVANCES IN CHEMICALLY-ACTIVATED MATERIALS (CAM'2014), 2014, 92 : 281 - 289