Microbially induced carbonate precipitation (MICP) has been widely studied for its broad application potential in geotechnical engineering. Exploring the pore-scale CaCO3 precipitation processes is one of the key aspects of fully understanding the mechanism of MICP for enhancing mechanical properties and controlling hydraulic properties of soils and rocks. Additionally, solution tests are typically the first step to understanding the reaction processes of MICP before conducting pore-scale and macro-scale tests. However, most explanations remain qualitative and do not establish a direct link between solution tests, pore-scale processes, and macro-scale performance. In this study, a saturation-dependent kinetic model is developed to describe the chemical reactions involved in MICP, and a phase-field model is employed to simulate the growth of CaCO3 crystals at the pore scale. The two models are coupled through the CaCO3 precipitation rate, enabling direct translation of solution test parameters into pore-scale simulations. Model predictions are validated against experimental data from microdroplet tests, showing good agreement in crystal growth dynamics under varying bacterial densities. The results demonstrate the capability of the proposed approach to quantitatively link solution chemistry with pore-scale mineralization processes. This work provides a robust framework for further investigation of MICP-induced pore sealing and particle bridging, contributing to the optimization and design of bio-mediated ground improvement strategies.
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