吸附
微型多孔材料
碳化
聚合物
碳纤维
氮气
材料科学
活性炭
羧酸
选择性
表面改性
化学工程
化学
有机化学
无机化学
高分子化学
催化作用
物理化学
复合材料
复合数
工程类
作者
Kai Ge,Yuting He,Wenyi Cai,Linyan Cheng,Cheng Fang,Jing Ding,Hui Wan,Guofeng Guan
标识
DOI:10.1016/j.jece.2022.107849
摘要
Nitrogen-doped microporous carbon materials were fabricated by carbonization of 1,8-diazabicyclo[5.4.0]undec-7-ene modified carboxylic acid polymers (PDA-DBU) without extra additional activators. The introduction of DBU could not only increase surface nitrogen content that enhanced the alkaline adsorption sites of carbon material itself, but also improved its specific surface area and pore volume. Therefore, CO 2 capture capacity of the nonactivated porous carbon (PDA-DBU-800) was 2.98 mmol·g −1 under 1 bar at 25 °C and the CO 2 adsorption selectivity based on the IAST adsorbed solution theory was 27.3 (CO 2 /N 2 =85:15). Meanwhile, the dynamic breakthrough experiment further confirmed that PDA-DBU adsorbent exhibited good selective adsorption capacity for CO 2 . Furthermore, PDA-DBU owned a great stability and reusability. The microporous carbon materials derived from DBU-modified carboxylic acid polymers will be a potential candidate for CO 2 capture. Nitrogen-doped microporous carbon materials were fabricated by carbonization of PDA-DBU without extra additional activators. The CO 2 capture capacity of PDA-DBU-800 was 2.98 mmol·g −1 under 1 bar at 25 °C and the CO 2 adsorption selectivity was 27.3 (CO 2 /N 2 =85:15), which was comparable or even better than those of the reported carbon-based adsorbents. • PDA-DBU derived nitrogen-doped microporous carbon materials were fabricated. • The introduction of DBU increased surface nitrogen content, activated carbon skeleton and generated micropore. • The synergy between micropores and basic sites enhanced CO 2 adsorption capacity and selectivity.
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