枯竭石灰岩含水层注入二氧化碳过程中温度对流体-岩石相互作用的影响:实验室和模拟研究

F. Azuddin, I. Davis, Michael A. Singleton, S. Geiger, E. Mackay, Duarte Silva
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引用次数: 3

摘要

当向含水层注入二氧化碳时,注入的二氧化碳通常比储层岩石冷;这导致沿流动路径的热梯度。温度的变化对CO2的溶解度和任何矿物反应的动力学都有影响。通过岩心驱流实验和相关的反应输运模拟,分析了在白云岩含水层中注入二氧化碳时的热效应,并量化了二氧化碳溶解度和矿物反应性是如何受到影响的。实验是通过将酸化盐水注入Edwards石灰石岩心样品进行的。背压为400psi,注入速度分别为30ml /hr和300ml /hr。测试温度范围从21°C到70°C。分析了出口流体成分的变化以及孔隙度和渗透率的变化。采用成分模拟模型对实验结果进行了进一步分析。通过改变反应表面积和动力学速率参数,模拟结果与实验数据进行了历史匹配。然后使用校准后的模型测试对CO2注入速度和温度的敏感性。从矿物体积、孔隙度和渗透率的变化观察温度对co2诱导矿物反应的影响。根据出口溶液浓度估计的反应速率常数比现有的单个矿物的数据低得多。估算的碳酸盐矿物比表面积与已公布的值基本一致。数值研究表明,在较低的温度下,尽管反应速度较慢,但矿物质的溶解度较高,因此,由于这些相互竞争的影响,在流出物中观察到适度升高的钙和镁浓度。在较高的温度下,矿物的溶解度较低,但现在反应速率较高,因此可以达到相似的出水浓度。然而,在较高的流量下,以较低的Damköhler为特征,停留时间较短,因此观察到较低的出水浓度。此外,方解石和白云石的溶解度随温度的变化有不同程度的变化,因此出水盐水中钙镁摩尔比随温度的升高而升高。在CO2注入过程中,近井区和深层储层的矿物组成变化不同。在温度较低的井附近,溶解度升高,但动力学反应速率和停留时间较低,在一定程度上限制了溶解。在含水层深处,溶解度将降低,停留时间将延长,从而能够建立平衡。因此,需要建立模型来连接这些流动状态。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of Temperature on Fluid-Rock Interactions During CO2 Injection in Depleted Limestone Aquifers: Laboratory and Modelling Studies
When CO2 is injected into an aquifer, the injected CO2 is generally colder than the reservoir rock; this results in thermal gradients along the flow path. The temperature variation has an impact on CO2 solubility and the kinetics of any mineral reactions. Core flood experiments and associated reactive transport simulations were conducted to analyse thermal effects during CO2 injection in a dolomitic limestone aquifer and to quantify how CO2 solubility and mineral reactivity are affected. The experiments were conducted by injecting acidified brine into an Edwards Limestone core sample. A back pressure of 400 psi and injection rates of 30 mL/hr and 300 mL/hr were used. A range of temperatures from 21 °C to 70 °C were examined. Changes in the outlet fluid composition and changes in porosity and permeability were analysed. A compositional simulation model was used to further analyse the experiments. The simulations were history-matched to the experimental data by changing the reactive surface area and the kinetic rate parameter. The calibrated model was then used to test the sensitivity to CO2 injection rate and temperature. The impact of temperature on CO2-induced mineral reactions was observed from changes in mineral volume, porosity and permeability. The reaction rate constants estimated from the outlet solution concentrations are much lower than existing data for individual minerals. The estimated specific surface areas for carbonate minerals are in reasonable agreement with published values. The numerical investigations showed that at the lower temperatures, despite the reaction rates being slower, the solubility of the minerals was higher, and so as a result of these competing effects, moderately elevated calcium and magnesium concentrations were observed in the effluent. At higher temperatures, the solubilities of the minerals were lower, but now the reactions rates were higher, so similar effluent concentrations could be achieved. However, at higher flow rates, characterized by a lower Damköhler number, the residence times were shorter, and so lower effluent concentrations were observed. Additionally, the solubilities of calcite and dolomite varied to different extents with temperature, and so the calcium to magnesium molar ratio in the effluent brine increased with increasing temperature. The change in mineral composition during CO2 injection varies between the near well zone and the deeper reservoir. Near the well where the temperatures will be lower, solubilities are elevated, but the kinetic reaction rates and residence times will be lower, somewhat limiting dissolution. Deeper in the aquifer the solubilities will be reduced and residence times will be longer, enabling an equilibrium to be established. Modelling is thus required to connect these flow regimes.
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