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

Bengtsson, Andreas (author)
RISE,Material- och ytdesign,Division Bioeconomy and Health, RISE Research Institutes of Sweden, P.O. Box 5604, SE-114 86 Stockholm, Sweden
Bengtsson, Jenny (author)
RISE,Polymera material och kompositer,Division Material and Production, RISE Research Institutes of Sweden, P.O. Box 104, SE-431 22 Mölndal, Sweden
Jedvert, Kerstin (author)
RISE,Polymera material och kompositer,Division Material and Production, RISE Research Institutes of Sweden, P.O. Box 104, SE-431 22 Mölndal, Sweden
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Kakkonen, Markus (author)
Fibrobotics OY, Korkeakoulunkatu 1, FI-33720 Tampere, Finland
Tanhuanpää, Olli (author)
Fibrobotics OY, Korkeakoulunkatu 1, FI-33720 Tampere, Finland
Brännvall, Elisabet (author)
RISE,Bioekonomi och hälsa,Division Bioeconomy and Health, RISE Research Institutes of Sweden, P.O. Box 5604, SE-114 86 Stockholm, Sweden
Sedin, Maria, PhD (author)
RISE,Material- och ytdesign,Division Bioeconomy and Health, RISE Research Institutes of Sweden, P.O. Box 5604, SE-114 86 Stockholm, Sweden
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 (creator_code:org_t)
2022-05-05
2022
English.
In: ACS Omega. - : American Chemical Society (ACS). - 2470-1343. ; 7:19, s. 16793-16802
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • : The demand for carbon fibers (CFs) based onrenewable raw materials as the reinforcing fiber in composites forlightweight applications is growing. Lignin−cellulose precursorfibers (PFs) are a promising alternative, but so far, there is limitedknowledge of how to continuously convert these PFs underindustrial-like conditions into CFs. Continuous conversion is vitalfor the industrial production of CFs. In this work, we havecompared the continuous conversion of lignin−cellulose PFs (50wt % softwood kraft lignin and 50 wt % dissolving-grade kraft pulp)with batchwise conversion. The PFs were successfully stabilizedand 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 atensile strength of 710−920 MPa. In comparison, CFs obtained at 1000 °C via batchwise conversion (12−15 μm diameter) with arelative 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 moduluscan 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.

Subject headings

TEKNIK OCH TEKNOLOGIER  -- Materialteknik -- Pappers-, massa- och fiberteknik (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Materials Engineering -- Paper, Pulp and Fiber Technology (hsv//eng)
TEKNIK OCH TEKNOLOGIER  -- Materialteknik -- Kompositmaterial och -teknik (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Materials Engineering -- Composite Science and Engineering (hsv//eng)

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