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    基于喷雾团聚熔盐改性MgO基CO2吸附剂颗粒脱碳性能

    Decarbonization performance of MgO-based CO2 adsorbent particles modified by spray agglomeration with molten saltst

    • 摘要: MgO基吸附剂的脱碳在CO2捕集和碳减排领域具有广阔的应用前景。然而,早期采用传统的成型方法,如浸渍法、挤压−滚圆法和溶胶−凝胶法以及球磨法,在工业放大过程中遇到了许多挑战。因此,迫切需要一种便于大规模生产的技术。喷雾团聚的成型方法是一种很有应用前景的技术,但在合成MgO基吸附剂方面的适用性仍需进一步验证。研究采用了商用MgO,再通过碱金属硝酸盐熔盐掺杂改性,通过浸渍法和喷雾团聚法合成了MgO与碱金属硝酸盐熔盐物质的量比为1.00∶0.15的MgO基吸附剂,并基于微型流化床反应器结合比表面积和孔体积、CO2程序升温脱附、扫描电子显微镜等手段对吸附剂的CO2吸附性能、表面形态以及实际物质的量比等参数进行了表征。结果表明:相同组分掺杂下,采用喷雾团聚法制备的吸附剂的CO2捕集量均优于浸渍法,尤其是MgO-NaK0.15-SA吸附剂在体积分数为10% CO2的混合气体中的CO2捕集容量为4.11 mmol/g。进一步研究了不同工况下MgO-NaK0.15-SA吸附剂的CO2捕集容量。结果显示反应温度为300 ℃,CO2体积分数为25%,混合气体流速为500 mL/min时MgO-NaK0.15-SA吸附剂的脱碳性能最佳,CO2捕集容量为7.84 mmol/g。研究了MgO-NaK0.15-SA吸附剂的循环稳定性,结合比表面积和孔体积以及实际物质的量比对吸附剂的循环衰减做出解释。研究为开发应用高效的MgO基吸附剂提供了新的见解和方向。

       

      Abstract: MgO-based adsorbents hold broad application prospects in the fields of CO2 capture and carbon emission reduction. However, traditional shaping methods, such as impregnation, extrusion-rolling, sol-gel, and ball milling, encountered numerous challenges during the industrial scaling-up process. Therefore, there is an urgent need for a technology that facilitates large-scale production. Spray agglomeration is a promising technology, but its applicability in the synthesis of MgO-based adsorbents still requires further validation. The study used commercial magnesium oxide, which was modified by doping with alkali metal nitrate molten salts, to synthesize MgO-based adsorbents with a molar ratio of MgO to alkali metal nitrate molten salts of 1∶0.15 using impregnation and spray agglomeration methods. The CO2 adsorption performance, surface morphology, and actual molar ratio of the adsorbents were characterized using a micro fluidized bed reactor combined with specific surface area and pore volume, CO2 temperature-programmed desorption, and scanning electron microscopy. The results showed that under the same component doping conditions, the CO2 capture capacity of the adsorbents prepared by the spray agglomeration method was superior to that of the impregnation method, especially for the MgO-NaK0.15-SA adsorbent, which had a CO2 capture capacity of 4.11 mmol/g in a mixed gas containing 10% CO2. Further research on the CO2 capture capacity of MgO-NaK0.15-SA adsorbent under different conditions showed that the best decarbonization performance of the MgO-NaK0.15-SA adsorbent was achieved at a reaction temperature of 300 ℃, a CO2 concentration of 25%, and a mixed gas flow rate of 500 mL/min, with a CO2 capture capacity of 7.84 mmol/g. The study also investigated the cyclic stability of the MgO-NaK0.15-SA adsorbent and explained the cyclic decay of the adsorbent by combining specific surface area, pore volume, and actual molar ratio. This study provides new insights and directions for the development and application of efficient MgO-based adsorbents.

       

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