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由低温稳定化线性低密度聚乙烯纤维制备的活性炭纤维的合成与表征

Synthesis and Characterization of Activated Carbon Fibers Derived from Linear Low-Density Polyethylene Fibers Stabilized at a Low Temperature.

作者信息

Kim Kwan-Woo, Lee Hye-Min, Kang Seong-Hyun, Kim Byung-Joo

机构信息

R&D Office 1st, Korea Carbon Industry Promotion Agency, Jeonju 54852, Korea.

Department of Organic Materials & Fiber Engineering, Jeonbuk National University, Jeonju 54896, Korea.

出版信息

Polymers (Basel). 2021 Nov 12;13(22):3918. doi: 10.3390/polym13223918.

DOI:10.3390/polym13223918
PMID:34833216
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8625871/
Abstract

In this study, activated carbon fibers (ACFs) were prepared using a new method from polyethylene (PE) fibers. The stabilizing (or crosslinking) process of PE, an essential step, was achieved through a hybrid treatment using electron-beam/sulfuric acid at 110 °C that was more effective than the traditional method of using sulfuric acid at 180 °C for polyolefin. The stabilized precursor was then carbonized at 700 °C and activated at 900 °C with different activation times. The structural characteristics and morphologies of these ACFs were observed using an X-ray diffractometer and a field-emission scanning electron microscope, respectively. In addition, the N/77K adsorption isotherm was used to discern textural properties. The total pore volume and specific surface area of these ACFs were found to be increased with a longer activation time, reaching final values of 0.99 cm/g and 1750 m/g, respectively. These ACFs also exhibited a high mesopore volume ratio (39%) according to crosslinking and crystallite formation conditions.

摘要

在本研究中,采用一种新方法由聚乙烯(PE)纤维制备了活性炭纤维(ACF)。PE的稳定化(或交联)过程是一个关键步骤,通过在110℃下使用电子束/硫酸的混合处理实现,该方法比在180℃下对聚烯烃使用硫酸的传统方法更有效。然后将稳定化的前驱体在700℃碳化,并在900℃下以不同的活化时间进行活化。分别使用X射线衍射仪和场发射扫描电子显微镜观察这些ACF的结构特征和形貌。此外,采用N/77K吸附等温线来识别织构性质。发现这些ACF的总孔体积和比表面积随着活化时间的延长而增加,最终分别达到0.99 cm/g和1750 m/g。根据交联和微晶形成条件,这些ACF还表现出较高的中孔体积比(39%)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46a0/8625871/4215f275c200/polymers-13-03918-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46a0/8625871/6546afc7a397/polymers-13-03918-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46a0/8625871/fadd8b44a2ee/polymers-13-03918-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46a0/8625871/71b4e6df304d/polymers-13-03918-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46a0/8625871/6c444a323384/polymers-13-03918-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46a0/8625871/3c709f6fd892/polymers-13-03918-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46a0/8625871/1f2545ddb03e/polymers-13-03918-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46a0/8625871/6e62f936c82e/polymers-13-03918-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46a0/8625871/3ccd4e94f53c/polymers-13-03918-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46a0/8625871/a80f7b1603fe/polymers-13-03918-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46a0/8625871/4215f275c200/polymers-13-03918-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46a0/8625871/6546afc7a397/polymers-13-03918-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46a0/8625871/fadd8b44a2ee/polymers-13-03918-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46a0/8625871/71b4e6df304d/polymers-13-03918-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46a0/8625871/6c444a323384/polymers-13-03918-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46a0/8625871/3c709f6fd892/polymers-13-03918-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46a0/8625871/1f2545ddb03e/polymers-13-03918-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46a0/8625871/6e62f936c82e/polymers-13-03918-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46a0/8625871/3ccd4e94f53c/polymers-13-03918-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46a0/8625871/a80f7b1603fe/polymers-13-03918-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46a0/8625871/4215f275c200/polymers-13-03918-g010.jpg

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Phys Rev A. 1990 Sep 15;42(6):3382-3387. doi: 10.1103/physreva.42.3382.