At present, the preparation of highly porous graphitic activated carbons (HPGACs) using the usual physical and chemical activation methods has met a bottleneck. In this study, HPGACs are directly synthesized from lignite at 900 °C. The whole process is completed by a microwave pretreatment, a graphitization conversion of the carbon framework at a low temperature using a small amount of FeCl3 (10–30 wt%), and a subsequent physical activation using CO2. Consequently, the dispersed and mobile iron species, in the absence of oxygen functional groups (removed during the microwave pretreatment), can greatly promote catalytic graphitization during pyrolysis, and, as an activating catalyst, can further facilitate the porosity development during activation. The as-obtained AC-2FeHLH-5-41.4(H) presents a low defect density, high purity, and specific surface area of 1852.43 m2 g−1, which is far greater than the AC-HLH-5-55.6(H) obtained solely by physical activation. AC-2FeHLH-5-41.4(H) as a supercapacitor electrode presents an excellent performance in the further electrochemical measurements. Such a convenient and practical method with low cost proves a scalable method to prepare HPGACs from a wide range of coal/biomass materials for industrial scale-up and applications.

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The utilization of coal-based activated carbons focuses on improving the physicochemical structure for achieving high-capacity. Herein, the catalytic effect of NaCl (1 and 3 wt%) in the presence of oxygen functional groups on the improvement of the physicochemical structure of coal-based activated carbons is studied in this work. A large quantity of Na can be retained in 1NaJXO and 3NaJXO with the presence of oxygen functional groups to promote further its catalytic characteristics during pyrolysis, resulting in the disordered transformation of the carbon structure. In addition, the development of micropores is mainly affected by the distribution and movement of Na catalyst, whereas the growth of mesopores is mainly influenced by the evolution of oxygen functional groups. Then, the active sites of 3NaJXO-800 can no longer be consumed preferentially in the presence of Na catalyst during subsequent CO 2 activation to facilitate the sustained disordered conversion of the microstructure and the rapid development of the micropores, resulting in the obvious high S BET value as activation proceeds. And the high S BET /burn-off ratio value (41.48 m 2 ·g −1 /%) of 3NaJXO-800 with a high value of S BET (1995.35 m 2 ·g −1 ) at a low burn-off value (48.1%) can be obtained, presenting the high efficiency of pore formation. Finally, the SO 2 adsorption efficiency of 3NaJXO-800-48.1 maintains at 100% within 90 min. After 180 min, 3NaJXO-800-48.1 still presents a high adsorptive capacity (140.2 mg/g). It is observed that a large micropore volume in the case of hierarchical pore structure necessarily assures optimal adsorption of SO 2 .

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Eggshell is a cheap and environmentally friendly calcium source. In this study, Ca-modified biochar adsorbents (CEA) were prepared by 1:10, 1:2, and 1:1 mass ratio of the eggshell and Eupatorium adenophorum. The CEA-2 sample prepared with a 1:2 mass ratio showed a maximum Pb adsorption capacity (97.74 mg·g –1 ) at the conditions of an initial pH of 7.0, an adsorbent dosage of 0.5 g·L –1 , and a contact time of 8.0 h. The kinetic and isotherm studies indicated that the adsorption process of the CEA-2 sample had monolayer adsorption characteristics, which was controlled together by intraparticle and interface diffusion. Thermodynamic studies indicated that the adsorption process of CEA-2 was spontaneous (Δ G 0 <0) and endothermic (Δ H 0 > 0). X-ray diffraction and scanning electron microscopy analyses showed a uniform distribution of Ca–Pb precipitation on the CEA-2 surface, which proved that chemical precipitation was the main adsorption mechanism. Fourier transform infrared spectra found that CEA-2 had abundant active groups, especially nitrogen-containing functional groups, which could adsorb Pb through a surface complexation reaction. The Brunauer–Emmett–Teller surface area of CEA-2 was found to be 621 m 2 ·g –1 , and such developed pores could ensure the smooth diffusion of Pb. Finally, the effect of coexisting cation and anion experiment and the cyclic regeneration experiment indicated that CEA-2 had prominent stability and reusability for Pb adsorption.