Kutchko Barbara G, Strazisar Brian R, Dzombak David A, Lowry Gregory V, Thaulow Niels
United States Department of Energy, National Energy Technology Laboratory, Pittsburgh, Pennsylvania 15236, USA.
Environ Sci Technol. 2007 Jul 1;41(13):4787-92. doi: 10.1021/es062828c.
Experiments were conducted to assess the durability of cements in wells penetrating candidate formations for geologic sequestration of CO2. These experiments showed a significant variation in the initial degradation (9 days of exposure) based on the curing conditions. The high-temperature (50 degrees C) and high-pressure (30.3 MPa) curing environment increased the degree of hydration and caused a change in the microstructure and distribution of the Ca(OH)2(s) phase within the cement. Cement cured at 50 degrees C and 30.3 MPa (representing sequestration conditions) proved to be more resistant to carbonic acid attack than cement cured at 22 degrees C and 0.1 MPa. The cement cured at 50 degrees C and 30.3 MPa exhibited a shallower depth of degradation and displayed a well-defined carbonated zone as compared to cement cured under ambient conditions. This is likely due to smaller, more evenly distributed Ca(OH)2(s) crystals that provide a uniform and effective barrier to CO2 attack.
开展了实验以评估水泥在穿透二氧化碳地质封存候选地层的油井中的耐久性。这些实验表明,基于养护条件,初始降解(暴露9天)存在显著差异。高温(50摄氏度)和高压(30.3兆帕)养护环境提高了水化程度,并导致水泥中Ca(OH)₂(s)相的微观结构和分布发生变化。在50摄氏度和30.3兆帕(代表封存条件)下养护的水泥比在22摄氏度和0.1兆帕下养护的水泥更耐碳酸侵蚀。与在环境条件下养护的水泥相比,在50摄氏度和30.3兆帕下养护的水泥降解深度更浅,且呈现出界限分明的碳酸化区域。这可能是由于更小、分布更均匀的Ca(OH)₂(s)晶体为二氧化碳侵蚀提供了均匀有效的屏障。