玄武岩CO2原位矿化封存研究进展及展望

Advances and prospects of research on in-situ CO2 mineralization storage in basalts

  • 摘要:
    背景 玄武岩地层CO2封存具有快速矿化、封存安全性高的显著优势,逐渐成为国内外研究的热点。系统综述了CO2原位矿化封存机理、矿化作用下地层物性演化特征、CO2原位矿化封存矿场示范3个方面的研究现状,并提出未来研究方向。
    进展 (1)玄武岩地层CO2原位矿化封存本质上是CO2-水−岩相互作用的过程,主要通过原生硅酸盐矿物的溶解及次生碳酸盐矿物的沉淀实现。其中,原生矿物溶解为整个反应的“限速”步骤。现有研究多采用静态反应釜与动态岩心驱替实验,系统揭示了不同类型玄武岩中矿物的溶解−沉淀行为,并识别出矿物组成、粒度/比表面积、体系pH、温度及流体组分等关键因素对CO2矿化反应动力学与产物的调控机制。(2) CO2-水−岩反应通过矿物溶解−沉淀耦合作用,不仅改变地层矿物组成,还显著影响其宏观物理性质。具体表现为孔隙结构重构、孔−渗特征演化以及力学性质的强化或弱化,这些变化共同决定了CO2的长期封存效能与地质安全性。(3)以冰岛CarbFix和美国Wallula为代表的矿场示范工程,分别实践了两种差异化的技术路径:CarbFix采用CO2未饱和水溶液注入,以“转化”为核心逻辑,通过加速溶解与矿化实现CO2的快速固定,并创新引入同位素示踪技术实时监测反应进程;Wallula则沿用超临界CO2注入方式,以“储存”为主导,依托盖层与圈闭构造保障封存安全,并借助地球物理测井评估泄漏风险。两者为不同地质条件下玄武岩CO2封存项目的选址、设计与监测提供了重要技术借鉴。
    展望 尽管玄武岩CO2原位矿化封存技术已取得显著进展,目前相关研究仍存在若干关键瓶颈亟待突破:包括次生矿物的精准定性与定量表征、钝化层形成机制及其对反应动力学的抑制效应、实际复杂地质−化学耦合条件下CO2矿化影响因素的全局敏感性分析,以及多矿物系统中“多源−多汇”反应路径的解耦与识别等。这些问题的深入探究,是推动该技术从示范走向规模化应用的核心基础,对未来实现安全高效的CO2地质封存具有重要意义。

     

    Abstract:
    Background CO2 storage in basalts, enjoying distinct advantages of rapid mineralization and high safety, has gradually emerged as a hot research topic both in China and abroad. This study presents a systematic review of the current status of research on the mechanisms of in-situ CO2 mineralization storage, the evolutionary characteristics of the physical properties of strata under the condition of mineralization reactions, and representative demonstration projects. On this basis, the future research directions are proposed.
    Advances in Research  The in-situ CO2 mineralization storage in basalts is essentially a process of CO2-water-rock reactions, achieved primarily through both the dissolution of primary silicate minerals and the precipitation of secondary carbonate minerals, with the former limiting the speed of the whole reaction process. Through static autoclave experiments and dynamic core flooding experiments, existing studies have systematically revealed the dissolution and precipitation behavior of minerals in various types of basalts and have identified the mechanisms by which factors such as mineral composition, grain size/specific surface area, pH, temperature, and fluid composition regulate the kinetics and products of CO2 mineralization reactions. Through the coupling of mineral dissolution and precipitation, CO2 mineralization reactions alter the composition of minerals in strata while also significantly affecting their macroscopic physical properties, as manifested by pore structure reconstruction, porosity and permeability evolution, and mechanical property enhancement or weakness. These changes jointly determine the efficiency and geological safety of long-term CO2 storage. The two global representative demonstration projects, i.e., the CarbFix project in Iceland and the Wallula project in the United States, employ two different CO2 injection techniques. In the CarbFix project, CO2-unsaturated aqueous solution is injected into basalts, with conversion used as the core logic. In this project, accelerated dissolution and mineralization reactions are employed for rapid CO2 fixing, while isotope tracing technology is innovatively introduced to monitor the reaction process in real time. In contrast, the Wallula project focuses on CO2 storage. In this project, supercritical CO2 is injected into target strata, with caprocks and trap structures playing a key role in ensuring safe CO2 sequestration. Additionally, geophysical logging is adopted to assess the CO2 leakage risk. The two projects provide a valuable reference for the siting, design, and monitoring of CO2 storage in basalts under various geological conditions.
    Prospects  Although significant advances have been achieved in in-situ CO2 mineralization storage in basalts, there is a urgent need to make breakthroughs in some key issues, including (1) the accurate identification and quantitative characterization of secondary minerals; (2) the understanding of the formation mechanisms of passivation layers and their inhibiting effects on reactions; (3) global sensitivity analysis of factors influencing CO2 mineralization under actual complex geological-chemical coupling conditions; and (4) the decoupling and identification of multi-source and multi-sink reaction pathways in multi-mineral systems. Thoroughly investigating these issues will lay a core foundation for driving the large-scale applications of in-situ CO2 mineralization storage from demonstration, thus holding great significance for safe and efficient geological CO2 sequestration in the future.

     

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