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Continuous Stabilization and Carbonization of a Lignin–Cellulose Precursor to Carbon Fiber

[Image: see text] The demand for carbon fibers (CFs) based on renewable raw materials as the reinforcing fiber in composites for lightweight applications is growing. Lignin–cellulose precursor fibers (PFs) are a promising alternative, but so far, there is limited knowledge of how to continuously con...

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Autores principales: Bengtsson, Andreas, Bengtsson, Jenny, Jedvert, Kerstin, Kakkonen, Markus, Tanhuanpää, Olli, Brännvall, Elisabet, Sedin, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9118265/
https://www.ncbi.nlm.nih.gov/pubmed/35601329
http://dx.doi.org/10.1021/acsomega.2c01806
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author Bengtsson, Andreas
Bengtsson, Jenny
Jedvert, Kerstin
Kakkonen, Markus
Tanhuanpää, Olli
Brännvall, Elisabet
Sedin, Maria
author_facet Bengtsson, Andreas
Bengtsson, Jenny
Jedvert, Kerstin
Kakkonen, Markus
Tanhuanpää, Olli
Brännvall, Elisabet
Sedin, Maria
author_sort Bengtsson, Andreas
collection PubMed
description [Image: see text] The demand for carbon fibers (CFs) based on renewable raw materials as the reinforcing fiber in composites for lightweight applications is growing. Lignin–cellulose precursor fibers (PFs) are a promising alternative, but so far, there is limited knowledge of how to continuously convert these PFs under industrial-like conditions into CFs. Continuous conversion is vital for the industrial production of CFs. In this work, we have compared the continuous conversion of lignin–cellulose PFs (50 wt % softwood kraft lignin and 50 wt % dissolving-grade kraft pulp) with batchwise conversion. The PFs were successfully stabilized and carbonized continuously over a total time of 1.0–1.5 h, comparable to the industrial production of CFs from polyacrylonitrile. CFs derived continuously at 1000 °C with a relative stretch of −10% (fiber contraction) had a conversion yield of 29 wt %, a diameter of 12–15 μm, a Young’s modulus of 46–51 GPa, and a tensile strength of 710–920 MPa. In comparison, CFs obtained at 1000 °C via batchwise conversion (12–15 μm diameter) with a relative stretch of 0% and a conversion time of 7 h (due to the low heating and cooling rates) had a higher conversion yield of 34 wt %, a higher Young’s modulus (63–67 GPa) but a similar tensile strength (800–920 MPa). This suggests that the Young’s modulus can be improved by the optimization of the fiber tension, residence time, and temperature profile during continuous conversion, while a higher tensile strength can be achieved by reducing the fiber diameter as it minimizes the risk of critical defects.
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spelling pubmed-91182652022-05-20 Continuous Stabilization and Carbonization of a Lignin–Cellulose Precursor to Carbon Fiber Bengtsson, Andreas Bengtsson, Jenny Jedvert, Kerstin Kakkonen, Markus Tanhuanpää, Olli Brännvall, Elisabet Sedin, Maria ACS Omega [Image: see text] The demand for carbon fibers (CFs) based on renewable raw materials as the reinforcing fiber in composites for lightweight applications is growing. Lignin–cellulose precursor fibers (PFs) are a promising alternative, but so far, there is limited knowledge of how to continuously convert these PFs under industrial-like conditions into CFs. Continuous conversion is vital for the industrial production of CFs. In this work, we have compared the continuous conversion of lignin–cellulose PFs (50 wt % softwood kraft lignin and 50 wt % dissolving-grade kraft pulp) with batchwise conversion. The PFs were successfully stabilized and carbonized continuously over a total time of 1.0–1.5 h, comparable to the industrial production of CFs from polyacrylonitrile. CFs derived continuously at 1000 °C with a relative stretch of −10% (fiber contraction) had a conversion yield of 29 wt %, a diameter of 12–15 μm, a Young’s modulus of 46–51 GPa, and a tensile strength of 710–920 MPa. In comparison, CFs obtained at 1000 °C via batchwise conversion (12–15 μm diameter) with a relative stretch of 0% and a conversion time of 7 h (due to the low heating and cooling rates) had a higher conversion yield of 34 wt %, a higher Young’s modulus (63–67 GPa) but a similar tensile strength (800–920 MPa). This suggests that the Young’s modulus can be improved by the optimization of the fiber tension, residence time, and temperature profile during continuous conversion, while a higher tensile strength can be achieved by reducing the fiber diameter as it minimizes the risk of critical defects. American Chemical Society 2022-05-05 /pmc/articles/PMC9118265/ /pubmed/35601329 http://dx.doi.org/10.1021/acsomega.2c01806 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Bengtsson, Andreas
Bengtsson, Jenny
Jedvert, Kerstin
Kakkonen, Markus
Tanhuanpää, Olli
Brännvall, Elisabet
Sedin, Maria
Continuous Stabilization and Carbonization of a Lignin–Cellulose Precursor to Carbon Fiber
title Continuous Stabilization and Carbonization of a Lignin–Cellulose Precursor to Carbon Fiber
title_full Continuous Stabilization and Carbonization of a Lignin–Cellulose Precursor to Carbon Fiber
title_fullStr Continuous Stabilization and Carbonization of a Lignin–Cellulose Precursor to Carbon Fiber
title_full_unstemmed Continuous Stabilization and Carbonization of a Lignin–Cellulose Precursor to Carbon Fiber
title_short Continuous Stabilization and Carbonization of a Lignin–Cellulose Precursor to Carbon Fiber
title_sort continuous stabilization and carbonization of a lignin–cellulose precursor to carbon fiber
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9118265/
https://www.ncbi.nlm.nih.gov/pubmed/35601329
http://dx.doi.org/10.1021/acsomega.2c01806
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