卤水
固碳
多孔性
降水
盐(化学)
地质学
含水层
化学工程
矿物学
材料科学
二氧化碳
化学
地下水
岩土工程
气象学
物理化学
工程类
物理
有机化学
作者
Myeongsub Kim,Andrew Sell,David Sinton
出处
期刊:Lab on a Chip
[Royal Society of Chemistry]
日期:2013-01-01
卷期号:13 (13): 2508-2508
被引量:160
摘要
In this study, we develop a lab-on-a-chip approach to study pore-scale salt precipitation dynamics during CO2 sequestration in saline aquifers-a challenge with this carbon management strategy. Three distinct phases-CO2 (gas), brine (liquid), and salt (solid)-are tracked through microfluidic networks matched to the native geological formations. The resulting salt formation dynamics indicate porosity decreases of ~20% in keeping with large scale core studies. At the network scale, the salt precipitation front moves at a constant velocity, ~2% that of the superficial CO2 velocity in this case. At the pore-scale, we observe two dominant types of salt formation: (1) large bulk crystals, on the order of the pore size (20-50 μm), forming early within trapped brine phases; and (2) polycrystalline aggregated structures, ranging over broad length scales, forming late in the evaporation process and collecting/projecting from the CO2-brine interface. Together, these two salt formation mechanisms show particular propensity for pore blockage and reduced carbon storage capacity.
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