Highly mesoporous activated carbon fibers using high density polyethylene precursor with a multi-step stabilization technique for automobile carbon canister

活性炭 碳化 高密度聚乙烯 微型多孔材料 比表面积 材料科学 体积热力学 丁烷 吸附 介孔材料 化学工程 碳纤维 聚乙烯 解吸 纤维 复合材料 化学 有机化学 催化作用 物理 量子力学 复合数 工程类
作者
John H. Ahn,Hyemin Lee,Byung-Joo Kim
出处
期刊:Journal of Industrial and Engineering Chemistry [Elsevier BV]
卷期号:128: 578-585 被引量:2
标识
DOI:10.1016/j.jiec.2023.08.024
摘要

In this study, activated carbon fibers (ACFs) for automobile carbon canisters were produced using high-density polyethylene (HDPE) fibers treated with a multistep stabilization process as the precursor. The stabilization of the HDPE fibers involved the following sequential steps: (1) electron beam irradiation, (2) mild sulfonation, and (3) dry oxidation. The stabilized fibers were carbonized at 900℃ in a nitrogen atmosphere. The carbonized fibers were activated at 900℃ in a water-vapor atmosphere from 30-60 min. The textural properties of the activated carbon fibers were determined using N2/77K adsorption-desorption isotherms. The specific surface area ranged from 1090 to 1980 m2/g, and the total pore volume ranged from 0.56 to 1.11 cm3/g. The specific surface area, micropore volume, and mesopore volume increased with increasing activation time. The fractions of micropores and mesopores were similar across all conditions, whereas the yield decreased gradually until 50 min, and then exhibited a sharp decline at 60 min. The butane working capacity increased as much as 56.24% as the increase in activation time. This can be attributed to the increase in butane activity owing to the increase in micropore volume, along with a decrease in butane resistivity caused by the increase in mesopore volume at a specific diameter.
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