Experiments were conducted to assess the durability ofcements in wells penetrating candidate formations for geologicsequestration of CO
2. These experiments showed asignificant variation in the initial degradation (9 days ofexposure) based on the curing conditions. The high-temperature (50
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C) and high-pressure (30.3 MPa) curingenvironment increased the degree of hydration and causeda change in the microstructure and distribution of theCa(OH)
2(s) phase within the cement. Cement cured at 50
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Cand 30.3 MPa (representing sequestration conditions)proved to be more resistant to carbonic acid attack thancement cured at 22
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C and 0.1 MPa. The cement cured at50
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C and 30.3 MPa exhibited a shallower depth ofdegradation and displayed a well-defined carbonatedzone as compared to cement cured under ambient conditions.This is likely due to smaller, more evenly distributedCa(OH)
2(s) crystals that provide a uniform and effectivebarrier to CO
2 attack.