Department of Petroleum Engineering, Curtin University , 26 Dick Perry Avenue, Kensington, 6151 Western Australia, Australia.
Acc Chem Res. 2017 May 16;50(5):1134-1142. doi: 10.1021/acs.accounts.6b00602. Epub 2017 Apr 13.
Carbon geosequestration (CGS) has been identified as a key technology to reduce anthropogenic greenhouse gas emissions and thus significantly mitigate climate change. In CGS, CO is captured from large point-source emitters (e.g., coal fired power stations), purified, and injected deep underground into geological formations for disposal. However, the CO has a lower density than the resident formation brine and thus migrates upward due to buoyancy forces. To prevent the CO from leaking back to the surface, four trapping mechanisms are used: (1) structural trapping (where a tight caprock acts as a seal barrier through which the CO cannot percolate), (2) residual trapping (where the CO plume is split into many micrometer-sized bubbles, which are immobilized by capillary forces in the pore network of the rock), (3) dissolution trapping (where CO dissolves in the formation brine and sinks deep into the reservoir due to a slight increase in brine density), and (4) mineral trapping (where the CO introduced into the subsurface chemically reacts with the formation brine or reservoir rock or both to form solid precipitates). The efficiency of these trapping mechanisms and the movement of CO through the rock are strongly influenced by the CO-brine-rock wettability (mainly due to the small capillary-like pores in the rock which form a complex network), and it is thus of key importance to rigorously understand CO-wettability. In this context, a substantial number of experiments have been conducted from which several conclusions can be drawn: of prime importance is the rock surface chemistry, and hydrophilic surfaces are water-wet while hydrophobic surfaces are CO-wet. Note that CO-wet surfaces dramatically reduce CO storage capacities. Furthermore, increasing pressure, salinity, or dissolved ion valency increases CO-wettability, while the effect of temperature is not well understood. Indeed theoretical understanding of CO-wettability and the ability to quantitatively predict it are currently limited although recent advances have been made. Moreover, data for real storage rock and real injection gas (which contains impurities) is scarce and it is an open question how realistic subsurface conditions can be reproduced in laboratory experiments. In conclusion, however, it is clear that in principal CO-wettability can vary drastically from completely water-wet to almost completely CO-wet, and this possible variation introduces a large uncertainty into trapping capacity and containment security predictions.
碳封存(Carbon Geosequestration,CGS)已被确定为减少人为温室气体排放的关键技术,从而可以显著减缓气候变化。在 CGS 中,CO 从大型点源排放物(例如燃煤电厂)中捕获、净化,并注入地下深处的地质构造中进行处置。然而,CO 的密度低于原地形成卤水,因此由于浮力而向上迁移。为了防止 CO 回漏到地表,使用了四种捕集机制:(1)结构捕集(其中紧密的冠层岩石作为密封屏障,CO 不能通过),(2)残余捕集(其中 CO 羽流分裂成许多微米大小的气泡,由于毛细力而被固定在岩石的孔隙网络中),(3)溶解捕集(其中 CO 溶解在形成的卤水中,由于卤水密度略有增加而沉入储层深处),和(4)矿物捕集(其中引入地下的 CO 与形成的卤水或储层岩石或两者发生化学反应,形成固体沉淀物)。这些捕集机制的效率和 CO 通过岩石的运移强烈受到 CO-卤水-岩石润湿性的影响(主要是由于岩石中的小毛细状孔隙形成了复杂的网络),因此严格理解 CO 润湿性至关重要。在这种情况下,已经进行了大量的实验,从中可以得出几个结论:最重要的是岩石表面化学,亲水表面是水湿的,而疏水表面是 CO 湿的。请注意,CO 湿表面会大大降低 CO 的储存能力。此外,增加压力、盐度或溶解离子价会增加 CO 的润湿性,而温度的影响尚不清楚。事实上,对 CO 润湿性的理论理解和定量预测的能力目前受到限制,尽管最近取得了一些进展。此外,用于真实储层岩石和真实注入气体(其中包含杂质)的数据很少,因此如何在实验室实验中再现真实的地下条件是一个悬而未决的问题。总之,然而,很明显,CO 润湿性在原则上可以从完全水湿到几乎完全 CO 湿发生巨大变化,这种可能的变化给捕集能力和封存安全性预测带来了很大的不确定性。