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Experimental Investigation on the Behavior of Supercritical CO_2 during Reservoir Depressurization

机译:油藏减压过程中超临界CO_2行为的实验研究

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摘要

CO_2 sequestration in saline aquifers is a promising way to address climate change. However, the pressure of the sequestration reservoir may decrease in practice, which induces CO_2 exsolution and expansion in the reservoir. In this study, we conducted a core-scale experimental investigation on the depressurization of CO_2-containing sandstone using NMR equipment. Three different series of experiments were designed to investigate the influence of the depressurization rate and the initial CO_2 states on the dynamics of different trapping mechanisms. The pressure range of the depressurization was from 10.5 to 4.0 MPa, which covered the supercritical and gaseous states of the CO_2 (named as CO_2(sc) and CO_2(g)> respectively). It was found that when the aqueous phase saturated initially, the exsolution behavior strongly depended on the depressurization rate. When the CO_2 and aqueous phase coexisting initially, the expansion of the CO_2(sc/g) contributed to the incremental CO_2 saturation in the core only when the CO_2 occurred as residually trapped. It indicates that the reservoir depressurization has the possibility to convert the solubility trapping to the residual trapping phase, and/or convert the residual trapping to mobile CO_2.
机译:盐水层中的CO_2隔离是解决气候变化的一种有前途的方法。但是,螯合储层的压力实际上可能会降低,这会导致CO_2的释放和在储层中膨胀。在这项研究中,我们使用NMR设备对含CO_2砂岩降压进行了核心规模的实验研究。设计了三个不同系列的实验来研究降压速率和初始CO_2状态对不同捕集机制动力学的影响。降压的压力范围为10.5至4.0 MPa,涵盖了CO_2的超临界状态和气态(分别命名为CO_2(sc)和CO_2(g)>)。发现当水相最初饱和时,析出行为强烈取决于降压速率。当CO_2和水相最初共存时,仅当CO_2残留时,CO_2(sc / g)的膨胀才有助于岩心中CO_2饱和度的增加。这表明储层减压有可能将溶解度捕集转化为残留捕集相,和/或将残留捕集转化为流动的CO_2。

著录项

  • 来源
    《Environmental Science & Technology》 |2017年第15期|8869-8876|共8页
  • 作者单位

    Beijing Key Laboratory of CO_2 Utilization and Reduction Technology, Department of Thermal Engineering, Tsinghua University, Beijing, China,Key Laboratory for Thermal Science and Power Engineering of Ministry of Education, Tsinghua University, Beijing, China;

    Beijing Key Laboratory of CO_2 Utilization and Reduction Technology, Department of Thermal Engineering, Tsinghua University, Beijing, China,Key Laboratory for Thermal Science and Power Engineering of Ministry of Education, Tsinghua University, Beijing, China;

    Beijing Key Laboratory of CO_2 Utilization and Reduction Technology, Department of Thermal Engineering, Tsinghua University, Beijing, China,Key Laboratory for Thermal Science and Power Engineering of Ministry of Education, Tsinghua University, Beijing, China;

    Beijing Key Laboratory of CO_2 Utilization and Reduction Technology, Department of Thermal Engineering, Tsinghua University, Beijing, China,Key Laboratory for Thermal Science and Power Engineering of Ministry of Education, Tsinghua University, Beijing, China;

    Beijing Key Laboratory of CO_2 Utilization and Reduction Technology, Department of Thermal Engineering, Tsinghua University, Beijing, China,Key Laboratory for Thermal Science and Power Engineering of Ministry of Education, Tsinghua University, Beijing, China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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