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水载超临界 CO2 中硅灰石碳酸化:粒度的影响。

Wollastonite Carbonation in Water-Bearing Supercritical CO: Effects of Particle Size.

机构信息

Department of Energy, Environmental and Chemical Engineering, Washington University , Saint Louis, Missouri 63130, United States.

Earth and Environmental Science, Lawrence Berkeley National Laboratory , Berkeley, California 94720, United States.

出版信息

Environ Sci Technol. 2017 Nov 7;51(21):13044-13053. doi: 10.1021/acs.est.7b04475. Epub 2017 Oct 18.

DOI:10.1021/acs.est.7b04475
PMID:28968071
Abstract

The performance of geologic CO sequestration (GCS) can be affected by CO mineralization and changes in the permeability of geologic formations resulting from interactions between water-bearing supercritical CO (scCO) and silicates in reservoir rocks. However, without an understanding of the size effects, the findings in previous studies using nanometer- or micrometer-size particles cannot be applied to the bulk rock in field sites. In this study, we report the effects of particle sizes on the carbonation of wollastonite (CaSiO) at 60 °C and 100 bar in water-bearing scCO. After normalization by the surface area, the thickness of the reacted wollastonite layer on the surfaces was independent of particle sizes. After 20 h, the reaction was not controlled by the kinetics of surface reactions but by the diffusion of water-bearing scCO across the product layer on wollastonite surfaces. Among the products of reaction, amorphous silica, rather than calcite, covered the wollastonite surface and acted as a diffusion barrier to water-bearing scCO. The product layer was not highly porous, with a specific surface area 10 times smaller than that of the altered amorphous silica formed at the wollastonite surface in aqueous solution. These findings can help us evaluate the impacts of mineral carbonation in water-bearing scCO.

摘要

地质封存 CO2(GCS)的性能可能会受到 CO2 矿化以及含水超临界 CO2(scCO2)与储层岩石中硅酸盐之间相互作用导致的地质地层渗透率变化的影响。然而,如果不了解尺寸效应,之前使用纳米或微米级颗粒进行的研究结果就无法应用于现场的块状岩石。在这项研究中,我们报告了在含水 scCO2 中,60°C 和 100 巴条件下,颗粒大小对硅灰石(CaSiO3)碳酸化的影响。通过表面积归一化后,表面上反应的硅灰石层的厚度与颗粒大小无关。20 小时后,反应不再受表面反应动力学的控制,而是受含水 scCO2 在硅灰石表面产物层中的扩散控制。在反应产物中,无定形二氧化硅而不是方解石覆盖了硅灰石表面,并充当了含水 scCO2 的扩散屏障。产物层的孔隙度不高,比在水溶液中硅灰石表面形成的变质无定形二氧化硅的比表面积小 10 倍。这些发现可以帮助我们评估含水 scCO2 中矿物碳酸化的影响。

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