Incorporating Nanoscale Effects into a Continuum-Scale Reactive Transport Model for CO2-Deteriorated Cement
Author(s) -
Qingyun Li,
Carl I. Steefel,
YoungShin Jun
Publication year - 2017
Publication title -
environmental science and technology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.851
H-Index - 397
eISSN - 1520-5851
pISSN - 0013-936X
DOI - 10.1021/acs.est.7b00594
Subject(s) - brine , cement , portlandite , dissolution , nucleation , nanoscopic scale , materials science , characterisation of pore space in soil , chemical engineering , mineralogy , geology , geotechnical engineering , portland cement , chemistry , nanotechnology , composite material , porosity , organic chemistry , engineering
Wellbore cement deterioration is critical for wellbore integrity and the safety of CO 2 storage in geologic formations. Our previous experimental work highlighted the importance of the portlandite (CH)-depleted zone and the surface dissolution zone in the CO 2 -attacked cement. In this study, we simulated numerically the evolution of the CH-depleted zone and the dissolution of the cement surfaces utilizing a reduced-dimension (1D) reactive transport model. The approach shows that three nanoscale effects are important and had to be incorporated in a continuum-scale model to capture experimental observations: First, it was necessary to account for the fact that secondary CaCO 3 precipitation does not fill the pore space completely, with the result that acidic brine continues to diffuse through the carbonated zone to form a CH-depleted zone. Second, secondary precipitation in brine begins via nucleation kinetics, and this could not be described with previous models using growth kinetics alone. Third, our results suggest that the CaCO 3 precipitates in the confined pore space are more soluble than those formed in brine. This study provides a new platform for a reduced dimension model for CO 2 attack on cement that captures the important nanoscale mechanisms influencing macroscale phenomena in subsurface environments.
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