Microstructure of polyacrylonitrile-based activated carbon fibers prepared from solvent-free coagulation process

Polyacrylonitrile precursor fibers prepared using a solvent-free coagulation process were stabilized, carbonized, and physically activated by carbon dioxide into activated carbon fibers (ACFs). The activation temperature varied from 600 to 900°C while the activation time was 1 h. Atomic force micros...

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Main Authors: Yusof, Norhaniza, Rana, Dipak, Ismail, Ahmad Fauzi, Matsuura, Takeshi
Format: Article
Published: Universidad Nacional Autonoma de Mexico, Centro de Ciencias Aplicadas y Desarrollo Tecnologico 2016
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Online Access:http://eprints.utm.my/id/eprint/73916/
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84962163318&doi=10.1016%2fj.jart.2016.02.001&partnerID=40&md5=5c1a18bbe003504b1801960604c6dae7
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spelling my.utm.739162017-11-22T00:45:16Z http://eprints.utm.my/id/eprint/73916/ Microstructure of polyacrylonitrile-based activated carbon fibers prepared from solvent-free coagulation process Yusof, Norhaniza Rana, Dipak Ismail, Ahmad Fauzi Matsuura, Takeshi TP Chemical technology Polyacrylonitrile precursor fibers prepared using a solvent-free coagulation process were stabilized, carbonized, and physically activated by carbon dioxide into activated carbon fibers (ACFs). The activation temperature varied from 600 to 900°C while the activation time was 1 h. Atomic force microscopy was used to observe the surface morphology, as well as the surface roughness of the ACFs. Higher pyrolysis temperature formed rougher surfaces, and increased the pore sizes. Meanwhile, Fourier transform infrared spectroscopy revealed more conversion of oxygen containing functional groups to carbonaceous materials as the activation temperature increased. Moreover, the microstructure properties were thoroughly characterized by the X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) studies. XRD analysis showed that the activation of the ACFs shrank the ordered structure, reducing the D-spacing from 0.358 to 0.347 nm for the fibers prepared at activation temperatures of 600 to 900°C. Meanwhile, XPS analysis concluded that that the oxygen containing functional groups were still retained even at high activation temperatures while the nitrogen containing functional groups were reduced during the high temperature activation in the CO2 atmosphere. Universidad Nacional Autonoma de Mexico, Centro de Ciencias Aplicadas y Desarrollo Tecnologico 2016 Article PeerReviewed Yusof, Norhaniza and Rana, Dipak and Ismail, Ahmad Fauzi and Matsuura, Takeshi (2016) Microstructure of polyacrylonitrile-based activated carbon fibers prepared from solvent-free coagulation process. Journal of Applied Research and Technology, 14 (1). pp. 54-61. ISSN 1665-6423 https://www.scopus.com/inward/record.uri?eid=2-s2.0-84962163318&doi=10.1016%2fj.jart.2016.02.001&partnerID=40&md5=5c1a18bbe003504b1801960604c6dae7
institution Universiti Teknologi Malaysia
building UTM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Teknologi Malaysia
content_source UTM Institutional Repository
url_provider http://eprints.utm.my/
topic TP Chemical technology
spellingShingle TP Chemical technology
Yusof, Norhaniza
Rana, Dipak
Ismail, Ahmad Fauzi
Matsuura, Takeshi
Microstructure of polyacrylonitrile-based activated carbon fibers prepared from solvent-free coagulation process
description Polyacrylonitrile precursor fibers prepared using a solvent-free coagulation process were stabilized, carbonized, and physically activated by carbon dioxide into activated carbon fibers (ACFs). The activation temperature varied from 600 to 900°C while the activation time was 1 h. Atomic force microscopy was used to observe the surface morphology, as well as the surface roughness of the ACFs. Higher pyrolysis temperature formed rougher surfaces, and increased the pore sizes. Meanwhile, Fourier transform infrared spectroscopy revealed more conversion of oxygen containing functional groups to carbonaceous materials as the activation temperature increased. Moreover, the microstructure properties were thoroughly characterized by the X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) studies. XRD analysis showed that the activation of the ACFs shrank the ordered structure, reducing the D-spacing from 0.358 to 0.347 nm for the fibers prepared at activation temperatures of 600 to 900°C. Meanwhile, XPS analysis concluded that that the oxygen containing functional groups were still retained even at high activation temperatures while the nitrogen containing functional groups were reduced during the high temperature activation in the CO2 atmosphere.
format Article
author Yusof, Norhaniza
Rana, Dipak
Ismail, Ahmad Fauzi
Matsuura, Takeshi
author_facet Yusof, Norhaniza
Rana, Dipak
Ismail, Ahmad Fauzi
Matsuura, Takeshi
author_sort Yusof, Norhaniza
title Microstructure of polyacrylonitrile-based activated carbon fibers prepared from solvent-free coagulation process
title_short Microstructure of polyacrylonitrile-based activated carbon fibers prepared from solvent-free coagulation process
title_full Microstructure of polyacrylonitrile-based activated carbon fibers prepared from solvent-free coagulation process
title_fullStr Microstructure of polyacrylonitrile-based activated carbon fibers prepared from solvent-free coagulation process
title_full_unstemmed Microstructure of polyacrylonitrile-based activated carbon fibers prepared from solvent-free coagulation process
title_sort microstructure of polyacrylonitrile-based activated carbon fibers prepared from solvent-free coagulation process
publisher Universidad Nacional Autonoma de Mexico, Centro de Ciencias Aplicadas y Desarrollo Tecnologico
publishDate 2016
url http://eprints.utm.my/id/eprint/73916/
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84962163318&doi=10.1016%2fj.jart.2016.02.001&partnerID=40&md5=5c1a18bbe003504b1801960604c6dae7
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