Abstract

Wellbore cement is subjected to a number of mechanical, thermal and chemical stress regimes over its lifetime. Therefore, next-generation wellbore cement formulations need to be evaluated in conditions relevant to these environments. In this work, we investigate the mechanism of the alteration of a novel self-healing polymer-cement composite after exposure to a CO2-rich environment by using synchrotron-based X-ray Fluorescence (XRF), X-ray absorption near edge structure (XANES), and scanning electron microscopy coupled with energy dispersive spectroscopy. Results showed that a chemical alteration of the polymer-cement follows the rim carbonation mechanism, similar to conventional cement, although carbonation takes place to a lesser extent in polymer-cements despite the higher porosity. Along with detailed mechanistic insights on carbonation in polymer-cement composite, the performance of these in CO2-rich environment is further studied using standard compressive strength analysis.

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