Activated Carbon from Manchurian Walnut Shells for CO2 Adsorption: A Comparison of CO2 and KOH Activation Methods

IF 0.8 4区 工程技术 Q4 CHEMISTRY, MULTIDISCIPLINARY
O. V. Gorbunova, M. V. Trenikhin, A. V. Lavrenov
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Abstract

In this study, a two-stage approach was employed to produce porous carbons from Manchurian walnut shells (MNS). The shells were utilized as a cost-effective biomass precursor for activated carbon production. The first step involved the carbonization of the shells, followed by activation using either carbon dioxide or potassium hydroxide. As a result, two series of biochar samples were prepared by varying the duration of CO2 activation and the KOH-to-precursor ratio. This approach enabled an investigation of the CO2 capture potential of the MNS-derived activated carbons. The structural evolution of the biochars was characterized using N2 physisorption, scanning and transmission electron microscopy. The results revealed that the original cellular structure was well-preserved after carbonization, while the activation step led to its significant transformation. Notably, the specific surface area, total pore volume, and micropore volume achieved after KOH activation were more than three times higher than those after CO2 activation. Nevertheless, CO2 activation is more economical and simpler than the chemical KOH method. The microporous structure of the samples changed with the KOH/carbonized MNS ratio. As the amount of KOH increased, all textural properties improved, except for the volume of narrow micropores (size <0.8 nm). The CO2 adsorption capacities of all samples were measured at 298 K and 1 bar. The maximum CO2 uptake in each series was 3.0 and 4.0 mmol/g, respectively. These values are competitive within the current state of CO2 adsorbent development.

Abstract Image

东北核桃壳活性炭吸附CO2: CO2和KOH活化方法的比较
以东北核桃壳为原料,采用两阶段法制备多孔碳。这些壳被用作生产活性炭的具有成本效益的生物质前体。第一步是将壳碳化,然后用二氧化碳或氢氧化钾进行活化。因此,通过改变CO2活化时间和koh -前驱体比,制备了两个系列的生物炭样品。这种方法能够研究mns衍生活性炭的CO2捕获潜力。利用N2物理吸附、扫描电镜和透射电镜对生物炭的结构演化进行了表征。结果表明,炭化后的细胞结构得到了较好的保存,而活化后的细胞结构发生了明显的变化。值得注意的是,KOH活化后的比表面积、总孔体积和微孔体积比CO2活化后的大3倍以上。然而,CO2活化比化学KOH法更经济、更简单。样品的微孔结构随KOH/碳化MNS比的变化而变化。随着KOH用量的增加,除窄微孔(尺寸为0.8 nm)体积外,所有织构性能均有所改善。在298k和1bar条件下测定了样品的CO2吸附量。各系列最大CO2吸收量分别为3.0和4.0 mmol/g。这些值在目前二氧化碳吸附剂发展的状态下是有竞争力的。
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来源期刊
Solid Fuel Chemistry
Solid Fuel Chemistry CHEMISTRY, MULTIDISCIPLINARY-ENERGY & FUELS
CiteScore
1.10
自引率
28.60%
发文量
52
审稿时长
6-12 weeks
期刊介绍: The journal publishes theoretical and applied articles on the chemistry and physics of solid fuels and carbonaceous materials. It addresses the composition, structure, and properties of solid fuels. The aim of the published articles is to demonstrate how novel discoveries, developments, and theories may be used in improved analysis and design of new types of fuels, chemicals, and by-products. The journal is particularly concerned with technological aspects of various chemical conversion processes and includes papers related to geochemistry, petrology and systematization of fossil fuels, their beneficiation and preparation for processing, the processes themselves, and the ultimate recovery of the liquid or gaseous end products.
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