State Key Laboratory of Chemical Engineering and Department of Chemistry, East China University of Science and Technology, Shanghai, 200237, PR China.
ChemSusChem. 2012 Oct;5(10):1912-7. doi: 10.1002/cssc.201200355. Epub 2012 Aug 21.
The search for a better carbon dioxide (CO(2) ) capture material is attracting significant attention because of an increase in anthropogenic emissions. Porous materials are considered to be among the most promising candidates. A series of porous, nitrogen-doped carbons for CO(2) capture have been developed by using high-yield carbonization reactions from task-specific ionic liquid (TSIL) precursors. Owing to strong interactions between the CO(2) molecules and nitrogen-containing basic sites within the carbon framework, the porous nitrogen-doped compound derived from the carbonization of a TSIL at 500 °C, CN500, exhibits an exceptional CO(2) absorption capacity of 193 mg of CO(2) per g sorbent (4.39 mmol g(-1) at 0 °C and 1 bar), which demonstrates a significantly higher capacity than previously reported adsorbents. The application of TSILs as precursors for porous materials provides a new avenue for the development of improved materials for carbon capture.
由于人为排放的增加,寻找更好的二氧化碳(CO(2))捕获材料引起了人们的极大关注。多孔材料被认为是最有前途的候选材料之一。通过使用特定于任务的离子液体(TSIL)前体的高产碳化反应,开发了一系列用于 CO(2)捕获的多孔氮掺杂碳。由于 CO(2)分子与碳骨架中含氮碱性位之间的强相互作用,源自 TSIL 在 500°C 碳化的多孔氮掺杂化合物 CN500 表现出异常高的 CO(2)吸收能力,每克吸附剂可吸收 193mg 的 CO(2)(在 0°C 和 1 巴下为 4.39mmol/g),其容量明显高于先前报道的吸附剂。将 TSIL 用作多孔材料的前体为开发用于碳捕获的改进材料提供了新途径。