Carbon Dioxide Capture from Ambient Air Using Amine-Grafted Mesoporous Adsorbents

A. Wagner, B. Steen, G. Johansson, E. Zanghellini, P. Jacobsson, P. Johansson
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引用次数: 35

Abstract

Anthropogenic emissions of carbon dioxide (CO2) have been identified as a major contributor to climate change. An attractive approach to tackle the increasing levels of CO2 in the atmosphere is direct extraction via absorption of CO2 from ambient air, to be subsequently desorbed and processed under controlled conditions. The feasibility of this approach depends on the sorbent material that should combine a long lifetime with nontoxicity, high selectivity for CO2, and favorable thermodynamic cycling properties. Adsorbents based on pore-expanded mesoporous silica grafted with amines have previously been found to combine high CO2 adsorption capacity at low partial pressures with operational stability under highly defined laboratory conditions. Here we examine the real potential and functionality of these materials by using more realistic conditions using both pure CO2, synthetic air, and, most importantly, ambient air. Through a combination of thermogravimetric analysis and Fourier transform infrared (TGA-FTIR) spectroscopy we address the primary functionality and by diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy the observed degradation of the material on a molecular level.
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利用胺接枝介孔吸附剂从环境空气中捕集二氧化碳
人为排放的二氧化碳(CO2)已被确定为气候变化的主要因素。解决大气中不断增加的二氧化碳水平的一个有吸引力的方法是通过吸收周围空气中的二氧化碳直接提取,随后在受控条件下解吸和处理。这种方法的可行性取决于吸附剂材料,该材料应结合使用寿命长、无毒、对二氧化碳的高选择性和有利的热力学循环特性。先前已经发现,基于胺接枝的扩孔介孔二氧化硅的吸附剂在低分压下具有高的CO2吸附能力,并且在高度确定的实验室条件下具有操作稳定性。在这里,我们通过使用更现实的条件,包括纯二氧化碳、合成空气,以及最重要的环境空气,来检验这些材料的真正潜力和功能。通过热重分析和傅里叶变换红外(TGA-FTIR)光谱的结合,我们解决了主要功能,并通过漫反射红外傅里叶变换(DRIFT)光谱在分子水平上观察到材料的降解。
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