化学
木质素
化学工程
活性炭
吸附
碳纤维
氧气
苯酚
氮气
苯
生物量(生态学)
有机化学
材料科学
复合材料
工程类
地质学
海洋学
复合数
作者
Félix Mérimé Bkangmo Kontchouo,Yuchen Jiang,Jingyi Liang,Mengjiao Fan,Yuewen Shao,Lijun Zhang,Shu Zhang,Xun Hu
标识
DOI:10.1016/j.joei.2023.101288
摘要
KOH and K2C2O4 are frequently used for activation of biomass to produce activated carbon (AC) but they could impact the evolution of pore characteristics of AC and bio-oil/gas during activation in different ways. This was investigated herein by activation of cola nut shell with KOH or K2C2O4 at 600 to 800 °C. The results indicated that cracking and gasification reactions dominated with presence of either KOH or K2C2O4, diminishing the production of solid products and shifting main products from bio-oil to gases. Nevertheless, KOH was more active than K2C2O4 for cracking of carboxylic acids, furans, nitrogen-containing organics, diminishing their formation in bio-oil while promoting the formation of phenolics from lignin. Additionally, K2C2O4 was more effective than KOH in developing pores at a lower temperature of 600 °C but not at 800 °C (1232.20 cm2g-1 with K2C2O4 versus 1376.0 cm2g-1 with KOH). Nevertheless, K2C2O4 favored formation of macropores, which, however, did not help to enhance the adsorption of phenol. The in-situ IR characterization suggested that KOH or K2C2O4 were highly active to crack -OH and C=O, suppressing their transformation to unsaturated functionalities. Substantial amount of oxygen species could be retained in resulting AC, but mainly in the thermally more stable form of C-O-C bonds for bridging benzene rings.
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