笼状水合物
结晶
烟气
二氧化碳
环境压力
材料科学
盐(化学)
碳纤维
物理吸附
碳捕获和储存(时间表)
锂(药物)
化学工程
吸附
化学
有机化学
水合物
热力学
工程类
医学
生态学
物理
气候变化
生物
复合数
复合材料
内分泌学
作者
Zhiling Xiang,Congyan Liu,C. Chen,Xin Xiao,Thien S. Nguyen,Cafer T. Yavuz,Qiang Xü,Bo Liu
标识
DOI:10.1016/j.xcrp.2023.101383
摘要
Reversible CO2 capture and release under ambient conditions is crucial for energy-efficient carbon capture and storage. Here, we report the pressure swing crystallization of CO2 in a single-crystalline guanidinium sulfate-based clathrate salt under practical conditions of 52 kPa and 298 K, with a high CO2 density (0.252 g cm−3) and capacity (17 wt %). The captured CO2 is released as a pure stream through moderate means of pressure or temperature stimulation, all while the desorbed Gua2SO4 is ready for another cycle. The clathrate is selective exclusively to CO2 even in the presence of common flue gas components, such as water vapor and N2, owing to the specific electrostatic interaction between the CO2 and guanidinium cations. The mechanism unraveled through single-crystal studies is distinctively different from physisorption or chemisorption, opening up a promising venue for future carbon capture and storage technologies through rapid CO2 solidification using an abundant salt.
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