固废基充填材料CO2矿化与胶凝性能退化关联机制

Mechanisms governing CO2 mineral trapping and cementitious activity degradation of solid waste-based backfill materials

  • 摘要:
    目的 研究钢渣、粉煤灰、炉底灰3种典型碱性工业固废的CO2矿化封存效率差异及固碳产物胶凝活性退化规律,揭示其矿化机理,评估其在充填工程中的应用潜力,推动工业固废资源化与碳减排协同发展。
    方法 采用直接湿法矿化实验,系统研究固废-CO2反应动力学及产物特征;结合X射线衍射(XRD)、扫描电镜(SEM)、红外光谱(FTIR)和热重分析(TGA)表征矿化产物的物相组成与微观结构;以碳酸化固废制备胶结充填试块,对比分析其力学性能与孔隙结构演化规律。
    结果和结论  (1) CO2矿化降碱反应过程受Ca2+含量与溶出动力学调控,钢渣、粉煤灰、炉底灰溶液的pH分别呈现“两段式”“三段式”和“骤降式”变化趋势。(2) 0.3 MPa-25 ℃反应条件下,钢渣固碳量(CO2)最高(136.1 g/kg),显著优于粉煤灰(CO2)(81.86 g/kg)和炉底灰(CO2)(16.2 g/kg),产物分别以方解石型和霰石型CaCO3为主。(3)受活性钙消耗和界面效应影响,固碳后试块抗压强度下降45.65%~73.48%,其中钢渣基材料强度降幅最大(10.22→2.71 MPa),粉煤灰次之(9.8→3.61 MPa),炉底灰因矿化反应不完全降幅最小(7.82→4.25 MPa)。研究结果为工业固废-CO2矿化协同处置提供了理论支撑和技术参考。

     

    Abstract:
    Objective This study investigated three types typical alkaline industrial solid waste: steel slag, fly ash, and bottom ash, highlighting the differences in their CO2 mineral trapping efficiency and the degradation patterns of their cementitious activity after carbon fixation. The purpose is to reveal the mechanisms underlying CO2 mineral trapping in solid waste and evaluate their application potential in backfill engineering, thereby promoting the synergistic development of industrial solid waste recycling and carbon emission reduction.
    Methods Through experiments on CO2 mineral trapping using the direct wet method, the kinetics and product characteristics of solid waste-CO2 interactions were systematically investigated. In combination with X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and thermogravimetric analysis (TGA), the phase composition and microstructures of the products formed during CO2 mineral trapping were characterized. Finally, the cemented backfill specimens were prepared using carbonated solid waste, and their mechanical properties, along with the evolutionary patterns of their pore structures, were compared and analyzed.
    Results and Conclusions The alkalinity reduction process during CO2 mineral trapping was governed by the content and dissolution kinetics of Ca2+. The pH values of the solutions of steel slag, fly ash, and bottom ash exhibited rapid-stable decreases, slow-rapid-stable decreases, and a sudden decrease, respectively. Under the condition of 0.3 MPa and 25 ℃, steel slag demonstrated the highest carbon (CO2) fixation capacity (136.1 g/kg), significantly outperforming both fly ash (81.86 g/kg) and bottom ash (16.2 g/kg). The primary products of the solid waste included calcite CaCO3 (steel slag and bottom ash) and aragonite CaCO3 (fly ash). Influenced by the consumption of active calcium and the interfacial effect, the compressive strength of the specimens decreased by 45.65%-73.48% after carbon fixation. Specifically, the steel slag-based specimens exhibited the highest decreased amplitude (from 10.22 MPa to 2.71 MPa), followed by fly ash-based specimens (from 9.8 MPa to 3.61 MPa). In contrast, the bottom ash-based specimens showed a minimal decline in the compressive strength (from 7.82 MPa to 4.25 MPa) due to incomplete reactions during CO2 mineral trapping. The results of this study provide theoretical support and a technical reference for the synergy between the treatment of industrial solid waste and CO2 mineral trapping.

     

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