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A CHEMICAL MODEL FOR THE SEAWATER-CO2- CARBONATE SYSTEM – AQUEOUS AND SURFACE CHEMISTRY

机译:海水 - 二氧化碳碳酸盐体系的化学模型 - 水性和表面化学

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We present a chemical model of the aqueous and surface chemistry of a calcium carbonate rock in equilibrium with a brine and CO2(g). The predicted surface chemistry match zeta potential measurements reported in the literature. We calculate the surface charge and potential of a rock in equilibrium with high salinity brines, such as seawater and Ekofisk formation water in the temperature range 25-130°C. We show that a calcium carbonate (chalk) core exposed to seawater at high temperature will experience dissolution and mineralogical change. Experiments performed on Stevns Klint chalk (which is a very clean chalk with a high content of calcium carbonate) show a significant water weakening effect when exposed to seawater at high temperatures. These cores also behave more water wet at high temperatures. From our calculations, we find no clear evidence that the explanation for these experiments could be due to changes in surface potential or charge, simply because the temperature dependence in the surface potential is too weak. Instead we find that dissolution of calcite have the right temperature dependence. We therefore suggest that a dissolution process inside the core could explain the experimental results. We present calculations that show a nice correlation between the oil produced in six imbibition experiments, and the calculated amount of dissolved calcium inside the core.
机译:我们在盐水和CO 2(G)的平衡中呈现碳酸钙岩的水化学和表面化学的化学模型。预测的表面化学匹配文献中报告的Zeta电位测量。我们计算高盐度盐水平衡的岩石的表面电荷和电位,例如海水和Ekofisk地层水25-130℃。我们表明,在高温下暴露于海水的碳酸钙(粉笔)核心将体验溶解和矿物学变化。在STEVN klint粉笔(其具有高含量的碳酸钙含量非常干净的粉笔)进行的实验表明,在高温下暴露于海水时,显着的水弱化效果。这些芯也表现出更多的水在高温下湿润。从我们的计算中,我们发现没有明确的证据表明这些实验的解释可能是由于表面潜力或充电的变化,仅仅因为表面电位的温度依赖性太弱。相反,我们发现方解石的溶解具有正确的温度依赖性。因此,我们建议核心内的溶出过程可以解释实验结果。我们呈现了在六种吸收实验中产生的油之间的良好相关性,以及核心内的计算量的溶解钙。

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