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Updated: Sep 22, 2025

Towards Biomimicking Wood: Fabricated Free-standing Films of Nanocellulose, Lignin, and a Synthetic Polycation
Published on: June 17, 2014
Continuous Stabilization and Carbonization of a Lignin-Cellulose Precursor to Carbon Fiber
Andreas Bengtsson1, Jenny Bengtsson2, Kerstin Jedvert2
1Division Bioeconomy and Health, RISE Research Institutes of Sweden, P.O. Box 5604, SE-114 86 Stockholm, Sweden.
Abstract:
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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