In this work, graphene-derived N-enriched porous carbons were synthesized by urea modification and KOH activation of thermally shocked graphene oxide. The prepared sorbents were characterized by various techniques and investigated as potential CO 2 capture materials. The as-prepared sorbents possess high CO 2 adsorption capacity of 2.40 mmol/g (25 °C) and 3.24 mmol/g (0 °C) at 1 bar, which is higher than most graphene-based carbons reported previously. The nitrogen incorporation and narrow microporosity are the two major factors that determine CO 2 uptake for these graphene-derived carbonaceous adsorbents under ambient conditions. The adsorption kinetic data of the optimized sample were well-described by the classical Fick’s diffusion model with a high CO 2 diffusion rate. The fast CO 2 adsorption kinetics can be attributed to the short diffusion paths of this sample, which is composed of thin layers of graphene sheets. Moreover, these graphene-derived sorbents also demonstrate excellent stability and recyclability, high selectivity of CO 2 over N 2, suitable heat of adsorption, and excellent dynamic CO 2 capture capacity. As a result, these graphene-derived porous carbons deserve consideration for removal of CO 2 from exhausted flue gas.
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An et al. (2019) studied this question.
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