首页|一例超微孔氢键有机框架用于CO2/CH4和CO2/N2的分离

一例超微孔氢键有机框架用于CO2/CH4和CO2/N2的分离

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二氧化碳(CO2)的有效捕获和分离对能源的高效利用和温室效应等环境问题的解决具有重要意义.氢键有机框架(hydrogen-bonded organic framework,HOF)具有制备条件温和、易再生、溶液加工性能好等优点,对CO2的捕获和分离具有很大的应用潜力.本文使用一例高稳定性电荷辅助型氢键有机磺酸胍框架HOF-GS-10实现了从CH4和N2中有效捕获CO2.在298 K和100kPa条件下,该材料能吸附1.23 mmolg-1的CO2,对CO2/N2(1/1)和CO2/CH4(1/1)混合气体的理想吸附溶液理论(ideal adsorption solution theory,IAST)选择性分别为19.1和5.1,且展现出较低的CO2吸附热(Qst=27.1 kJ mol-1).通过穿透吸附分离实验证实了 HOF-GS-10对CO2/N2和CO2/CH4混合物的分离效果.本研究表明,电荷辅助型氢键有机框架在碳捕获和分离方面具有应用潜力.
An ultramicroporous hydrogen-bonded organic framework for efficient CO2/CH4 and CO2/N2 separation
Efficient capture and separation for carbon dioxide is of great significance for improving energy utilization and addressing environmental concerns such as the upgrading of natural gas,and greenhouse effect.Hydrogen-bonded organic frameworks(HOFs)have great potential for efficient capture and separation of CO2 due to their mild synthesis conditions,ease of regeneration and good solution processability.However,there is a great challenge in fully activation of HOFs for permanent porosity given that hydrogen bonds are relatively weak.In this study,an ultramicroporous hydrogen-bonded organic framework,HOF-GS-10,has been reported to achieve efficient CO2 capture of CH4 and N2.That HOF is assembled by guanidinium cations and 1,5-naphthalene disulfonate anions through charge-assisted hydrogen bonds,showing two-dimensional double-layered networks with honeycomb-like hydrogen bonding units.The HOF structure contains 1D pore channels with pore aperture size of 2.67 Å.By virtue of mild activation involving solvent exchange by acetone and further heating at relatively lower temperature,this HOF can be fully desolvated as verified by its experimental pore volumes.The measured pore volume of micropores in that HOF is 0.16 cm g,which is consistent with the theoretical pore volume of 0.15 cm3 g-1 from crystal structures.At 298 K and 100 kPa,the HOF material can adsorb 1.23 mmol g-1 CO2,which is higher than that for CH4(0.37 mmol g-1)and N2(0.09 mmol g-1),resulting in IAST(ideal adsorbed solution theory)selectivity of 19.1 and 5.1 for equimolar mixture of CO2/N2 and CO2/CH4,respectively.Additionally,the isosteric heat of that HOF material for CO2 adsorption at low coverage is only about 27.1 kJ mol-1.The modelling study by grand canonical Monte Carlo simulations indicates that CO2 molecules interact with the host framework through weak intermolecular interactions,which are stronger than those for CH4 and N2 molecules.Breakthrough experiments validated the separation performance of HOF for CO2/N2(v/v,50/50)and CO2/CH4(v/v,50/50).After flowing through the fixed-bed HOF material,the purity of N2 reaches to 98.52%when the cumulative injection amount of CO2 is 10.90 cm3g-1.On the other hand,the maximum purity of CH4 from CO2/CH4 mixture is up to 99.60%,when the cumulative injection amount of CO2 reaches to 9.06 cm3 g-1.In addition,that HOF can maintain its crystallinity upon heating at elevated temperature and exposure to various solvents.Overall,this work illustrates a successful example of challenging HOF activation,and also demonstrates that HOF has a certain potential application in carbon capture and separation.

hydrogen-bonded organic frameworkporous materialgas adsorption and separationCO2 capture

肖仙仙、李经鸿、薛玮、周浩龙、林锐标、陈小明

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中山大学,绿色化学与分子工程研究院,化学学院,生物无机与合成化学教育部重点实验室,广州 510275

汕头大学化学系,汕头 515063

氢键有机框架 多孔材料 气体吸附分离 CO2捕获

国家自然科学基金国家自然科学基金国家自然科学基金国家自然科学基金广东省"珠江人才计划"引进创新创业团队计划中山大学百人计划中山大学中央高校基本科研业务费专项资金

221013072209006122375221220011602017ZT07C06922qntd2301

2024

科学通报
中国科学院国家自然科学基金委员会

科学通报

CSTPCD北大核心
影响因子:1.269
ISSN:0023-074X
年,卷(期):2024.69(16)