吸附
碳化物
碳纤维
化学工程
材料科学
碳化物衍生碳
二氧化碳
碳化
多孔性
活性炭
微型多孔材料
无机化学
二氧化碳电化学还原
化学
纳米技术
复合材料
有机化学
吸附
碳纳米纤维
碳纳米管
复合数
工程类
作者
Volker Presser,John H. McDonough,Sun-Hwa Yeon,Yury Gogotsi
摘要
CO2 sorption at atmospheric and sub-atmospheric pressures is a key step towards carbon capture and sequestration (CCS) and materials capable of fast and efficient CO2 uptake are currently being studied extensively. Carbide-derived carbons (CDCs) show a very high sorption capacity for CO2 of up to 7.1 mol/kg at 0 °C and ambient pressure. This value is significantly higher than other carbon materials. Systematic experimental investigation of a large number of different CDCs derived from nano- and micrometer sized precursors with and without activation show a linear correlation between the CO2 uptake at a certain pressure and the pore volume. However, CO2 sorption is not limited by the total pore volume but only by pores smaller than a certain diameter. At 1 bar, pores smaller than 0.8 nm contribute the most to the CO2 uptake and at 0.1 bar pores smaller or equal to 0.5 nm are preferred. With lower total pressure, smaller pores contribute more to the measured amount of adsorbed CO2. The prediction of the CO2 uptake based on the pore volume for pores of a certain diameter is much more accurate than predictions based on the mean pore size or the specific surface area. This study provides guidelines for the design of materials with an improved ability to remove carbon dioxide from the environment at atmospheric and lower pressures.
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