Abstract

Fluid-shale interactions appear to significantly affect shale micromechanical properties, which regulate fracture network propagation during multistage hydraulic fracturing in shales and thus the gas production. While published works confirm that fluid-shale interactions can reduce Young's modulus and rock strength compared to dry shale samples, few attentions have been paid to unveil the nature of the physics with a combination of geochemical modelling and disjoining pressure isotherm, and fewer works have envisaged the effect of mineralogy (calcite-rich or quartz-rich rock) on shale weakening with presence of aqueous liquids. We hypothesize that fluid-mineral interactions likely generate electrical double layer force between mineral surfaces which would shift the disjoining pressure from strongly negative (mineral-air-mineral) to less negative or even positive (mineral-fluid-mineral) thus triggering Young's modulus reduction. To test the hypothesis, geochemical modellings including minerals dissolution (calcite, dolomite, quartz, pyrite and illite) and surface complexation were performed together with disjoining pressure isotherm using literature experimental data, accounting for the Young's modulus reduction induced by fluid-shale interactions.The geochemical modelling shows that the amount of mineral dissolution at in-situ condition is negligible, and thus may play a minor role in Young's modulus. Disjoining isotherm shows that both calcite and quartz (plane-plane geometry) give a strong negative disjoining pressure generated by van der Waals force and structural force in the presence of air, whereas the disjoining pressure can be shifted from strongly negative to less negative for calcite and even positive for quartz in presence of fluids due to the electrostatic force, suggesting a Young's modulus reduction due to the weaker adhesion in line with literature experimental data. This work provides an overall conceptual framework, which supports the hydraulic fracturing fluid design and treatment in shale reservoirs from geochemical and disjoining pressure isotherm perspectives.

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