Mineral Sequestration of Carbon Dixoide in a Sandstone-Shale System
Mineral Sequestration of Carbon Dixoide in a Sandstone-Shale System
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DOI:
10.1016/j.chemgeo.2004.12.015
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发表时间:
2004-07
期刊:
影响因子:
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通讯作者:
Tianfu Xu;J. Apps;K. Pruess
中科院分区:
文献类型:
--
作者:
Tianfu Xu;J. Apps;K. Pruess
A conceptual model of CO2injection in bedded sandstone–shale sequences has been developed using hydrogeologic properties and mineral compositions commonly encountered in Gulf Coast sediments. Numerical simulations were performed with the reactive fluid flow and geochemical transport code TOUGHREACT to analyze mass transfer between sandstone and shale layers and CO2immobilization through carbonate precipitation. Results indicate that most CO2sequestration occurs in the sandstone. The major CO2trapping minerals are dawsonite and ankerite. The CO2mineral-trapping capacity after 100,000 years reaches about 90 kg/m3of the medium. The CO2trapping capacity depends on primary mineral composition. Precipitation of siderite and ankerite requires Fe+2supplied mainly by chlorite and some by hematite dissolution and reduction. Precipitation of dawsonite requires Na+provided by oligoclase dissolution. The initial abundance of chlorite and oligoclase therefore affects the CO2mineral-trapping capacity. The sequestration time required depends on the kinetic rate of mineral dissolution and precipitation. Dawsonite reaction kinetics is not well understood, and sensitivity regarding the precipitation rate was examined. The addition of CO2as secondary carbonates results in decreased porosity. The leaching of chemical constituents from the interior of the shale causes slightly increased porosity. The limited information currently available for the mineralogy of natural high-pressure CO2gas reservoirs is also generally consistent with our simulation. The “numerical experiments” give a detailed understanding of the dynamic evolution of a sandstone–shale geochemical system.