碳化作用
微型多孔材料
吸附
化学工程
活性炭
介孔材料
材料科学
烟气
吸附剂
碳纤维
热液循环
碱金属
热解
比表面积
多孔性
水热碳化
化学
有机化学
碳化
催化作用
复合材料
复合数
工程类
作者
Mengyuan Zhu,Weiquan Cai,Francis Verpoort,Jiabin Zhou
标识
DOI:10.1016/j.cherd.2019.03.044
摘要
The pineapple waste-derived porous carbons with enhanced CO2 adsorption performance were successfully prepared by a facile hydrothermal carbonation and followed thermal activation using facile alkali metal oxalates instead of KOH or K2CO3 for chemical activation. Compared with macroporous-mesoporous carbons activated by Li2C2O4 and Na2C2O4, the microporous carbon activated by K2C2O4 at 700 °C with a relatively high specific surface area of 1076.3 m2 g−1 and big pore volume of 0.92 cm3 g-1 for narrow micropores (<1 nm)for narrow micropores (<1 nm) shows the highest adsorption capacities of 5.32 mmol g-1 at 0 °C, and 4.25 mmol g-1 at 25 °C under 1 bar, respectively. Furthermore, all the samples show high selectivities from 18.24 to 38.42 for CO2/N2 separation, stable cyclic capability with adsorption loss of 12.6–17.8% after twelve cycles at 25 °C and reasonable isosteric heat of CO2 adsorption. Especially, the microporous carbon activated by facile K2C2O4 at 700 °C shows speedy adsorption dynamics and excellent dynamic adsorption performance for simulated flue gas based on its breakthrough curve. In combination with the low-cost carbon source, the above advantages make the pineapple waste-derived porous carbons exceptionally potential sorbent to capture and separate CO2 under real conditions.
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