Activated Carbons Derived from High-Temperature Pyrolysis of Lignocellulosic Biomass

活性炭 热解 木质纤维素生物量 生物量(生态学) 木质素 化学 吸附 氮气 比表面积 碳纤维 介孔材料 化学工程 打赌理论 材料科学 有机化学 催化作用 复合材料 农学 复合数 工程类 生物
作者
Cristian I. Contescu,Sushovit Adhikari,Nidia Gallego,N. D. Evans,Bryan E. Biss
出处
期刊:C [Multidisciplinary Digital Publishing Institute]
卷期号:4 (3): 51-51 被引量:101
标识
DOI:10.3390/c4030051
摘要

Biomass pyrolysis to produce biofuel and hydrogen yields large amounts of charred byproducts with low commercial value. A study was conducted to evaluate their potential for being converted into higher value activated carbons by a low-cost process. Six chars derived from various lignocellulosic precursors were activated in CO2 at 800 °C to 30–35% weight loss, and their surface area and porosity were characterized by nitrogen adsorption at 77 K. It was found that, in similar activation conditions, the surface area of the activated carbons correlates with the activation energy of the oxidation reaction by CO2, which in turn varies inversely with the carbon yield after thermolysis in nitrogen at 1000 °C. Since lignin is the most thermally-stable component of lignocellulosic biomass, these results demonstrate, indirectly, that robust, lignin-rich vegetal precursors are to be preferred to produce higher quality activated carbons. The chars derived from white pine (pinus strobus) and chestnut oak (quercus prinus) were converted to activated carbons with the highest surface area (900–1100 m2/g) and largest mesopores volume (0.85–1.06 cm3/g). These activated carbons have properties similar to those of commercially-available activated carbons used successfully for removal of pollutants from aqueous solutions.
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