用胺浸树脂直接捕获空气中的二氧化碳:树脂孔结构和潮湿条件的影响

Jiali Hua , Xuehua Shen , Xianfeng Jiao , Han Lin , Guanghuan Li , Xin Sun , Feng Yan , Hao Wu , Zuotai Zhang
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引用次数: 0

摘要

利用固体胺吸附剂进行直接空气捕集(DAC)是一项很有前景的技术,可用于抑制大气中二氧化碳含量的增加。尽管做出了大量努力,但这类材料在超稀释条件下吸收二氧化碳和吸附动力学方面的改进仍然有限。而且目前的研究大多集中在粉末状吸附剂上,这些吸附剂需要造粒或制成装置才能应用于 DAC,从而导致二氧化碳吸收率进一步下降。本文使用一系列商用树脂颗粒(1.0 毫米)作为支撑物,发现 X5 在制备固体胺吸附剂时表现出良好的支撑特性。值得注意的是,X5 具有 1.90 cm3/g 的大孔隙率,并具有由中孔和大孔组成的分层双峰多孔网络。所制备的吸附剂(PEI@X5)具有相当高的聚乙烯亚胺(PEI)分散性,即使 PEI 含量高达 50%,也能表现出优异的二氧化碳吸附性能,在模拟环境空气条件(25 °C、400 ppm CO2)下的 TGA 或固定床中,二氧化碳吸附量高达 118 或 108 mg/g。此外,这些吸附剂还表现出极佳的循环稳定性,在 10 次吸附-再生循环中未观察到衰减现象。引入 25% 相对湿度(RH)的水蒸气可显著提高吸附剂对二氧化碳的吸收率,使其达到 130 mg/g,提升效率为 20.4%。然而,由于吸附水过多,50 %PEI@X5 孔隙中的部分 PEI 被浸出,因此相对湿度进一步增加会降低二氧化碳吸收率和吸附率。考虑到原材料的商业化生产、50 %PEI@X5 的简易合成及其卓越的二氧化碳捕获效率,这些发现为 DAC 技术开辟了新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Direct air capture of CO2 by amine-impregnated resin: The effect of resin pore structure and humid conditions

Direct air capture of CO2 by amine-impregnated resin: The effect of resin pore structure and humid conditions

Direct air capture (DAC) by solid amine adsorbents is a promising technology to curb the increasing atmospheric CO2 level. Despite extensive efforts, there are still limited improvements for this type of materials in their CO2 uptake and adsorption kinetics under ultra-dilute conditions. And most current research focuses on powdered adsorbents, which need to be granulated or fabricated into devices for DAC application, resulting in a further decline in CO2 uptake. Herein, a series of commercial resin particles (1.0 mm) were used as supports, and it was found that X5 exhibited favorable support characteristics in the preparation of solid amine adsorbents. Notably, X5 possessed a large pore volume of 1.90 cm3/g and featured a hierarchical bimodal porous network comprising mesopores and macropores. The prepared adsorbents (PEI@X5) had considerable polyethyleneimine (PEI) dispersion even at PEI content up to 50 %, and thus demonstrated excellent CO2 adsorption performances with high CO2 uptakes of 118 or 108 mg/g in TGA or fixed bed under simulated ambient air conditions (25 °C, 400 ppm CO2). Additionally, the adsorbents exhibited superb cyclic stability with no decay observed over 10 adsorption-regeneration cycles. The introduction of 25 % relative humidity (RH) of water vapor significantly improved the CO2 uptake of the adsorbent to 130 mg/g, with a lifting efficiency of 20.4 %. However, further increases in RH reduced the CO2 uptake and adsorption rate due to the excessive adsorption water, which leached part of PEI from the pores of 50 %PEI@X5. Considering the commercial production of raw materials, the facile synthesis of 50 %PEI@X5, and its superior CO2 capture efficiency, these findings open up new avenues for DAC technology.

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