Vinogradov Jan, Hidayat Miftah, Sarmadivaleh Mohammad, Derksen Jos, Vega-Maza David, Iglauer Stefan, Jougnot Damien, Azaroual Mohamed, Leroy Philippe
University of Aberdeen, School of Engineering, Elphinstone Road, AB24 3UE Aberdeen, United Kingdom.
University of Aberdeen, School of Engineering, Elphinstone Road, AB24 3UE Aberdeen, United Kingdom; Curtin University, Discipline of Petroleum Engineering, 26 Dick Perry Avenue, 6151 Kensington, Australia.
J Colloid Interface Sci. 2022 Mar;609:852-867. doi: 10.1016/j.jcis.2021.11.084. Epub 2021 Nov 20.
Electrochemical interactions at calcite-water interface are characterized by the zeta potential and play an important role in many subsurface applications. In this work we report a new physically meaningful surface complexation model that is proven to be efficient in predicting calcite-water zeta potentials for a wide range of experimental conditions. Our model uses a two-stage optimization for matching experimental observations. First, equilibrium constants are optimized, and the Stern layer capacitance is optimized in the second stage. The model is applied to a variety of experimental sets that correspond to intact natural limestones saturated with equilibrated solutions of low-to-high salinity, and crushed Iceland Spar sample saturated with NaCl at non-equilibrium conditions. The proposed linear correlation of the Stern layer capacitance with the ionic strength is the main novel contribution to our surface complexation model without which high salinity experiments cannot be modelled. Our model is fully predictive given accurately known conditions. Therefore, the reported parameters and modelling protocol are of significant importance for improving our understanding of the complex calcite-water interfacial interactions. The findings provide a robust tool to predict electrochemical properties of calcite-water interfaces, which are essential for many subsurface applications including hydrology, geothermal resources, CO sequestration and hydrocarbon recovery.
方解石 - 水界面的电化学相互作用以zeta电位为特征,并且在许多地下应用中发挥着重要作用。在这项工作中,我们报告了一种新的具有物理意义的表面络合模型,该模型已被证明能够在广泛的实验条件下有效地预测方解石 - 水的zeta电位。我们的模型采用两阶段优化来匹配实验观测结果。首先,优化平衡常数,然后在第二阶段优化斯特恩层电容。该模型应用于各种实验数据集,这些数据集对应于用低至高盐度的平衡溶液饱和的完整天然石灰石,以及在非平衡条件下用氯化钠饱和的破碎冰洲石样品。所提出的斯特恩层电容与离子强度的线性相关性是我们表面络合模型的主要新颖贡献,没有这一点就无法对高盐度实验进行建模。在已知准确条件的情况下,我们的模型具有完全预测性。因此,所报告的参数和建模协议对于增进我们对方解石 - 水复杂界面相互作用的理解具有重要意义。这些发现提供了一个强大的工具来预测方解石 - 水界面的电化学性质,这对于许多地下应用(包括水文、地热资源、二氧化碳封存和烃类采收)至关重要。