TY - JOUR
T1 - Effects of pyrolysis temperature on the chemical composition of refined softwood and hardwood lignins
AU - Diehl, Brett G.
AU - Brown, Nicole R.
AU - Frantz, Curtis W.
AU - Lumadue, Matthew R.
AU - Cannon, Fred
N1 - Funding Information:
Funding for this project was provided by USDA National Needs Graduate Fellowship Competitive Grant No. 2007-38420-17782 from the USDA National Institute of Food and Agriculture , and from NIFA grant #2011-67009-20049. Many thanks to Alan Benesi and Wenbin Luo for assistance with solid state NMR sample preparation and data collection. Josh Stapleton and Joe Stitt of the Penn State Materials Research Institute are acknowledged for their contributions to IR and Raman data collection and interpretation.
PY - 2013/8
Y1 - 2013/8
N2 - The current study uses nuclear magnetic resonance, Fourier-transform infrared spectroscopy and Raman spectroscopy to investigate the evolution of refined softwood and hardwood lignins under various pyrolytic exposures. Little chemical change occurred at pyrolysis temperatures of 250 and 300 C, whereas significant mass loss and chemical change was observed at 400 and 500 C. These losses were mainly attributed to evolution of methoxyl, hydroxyl, and propyl groups. Mass loss plateaued following pyrolysis at 500 C, but rearrangements continued to occur at higher temperatures, resulting in char that became increasingly polyaromatic in nature. Following brief pyrolytic exposures at 500 and 600 C, the refined hardwood and softwood lignins yielded coal-like products. Lignin pyrolyzed at higher temperatures yielded chars with greater order, similar in composition to coke. These coal and coke-like products are called "lignin-based carbon" (LBC). The polyaromatic nature of the LBC after high temperature pyrolysis was perceived as the result of radical formation and recombination, leading to fused aromatic structures, which occurs more readily at higher temperatures.
AB - The current study uses nuclear magnetic resonance, Fourier-transform infrared spectroscopy and Raman spectroscopy to investigate the evolution of refined softwood and hardwood lignins under various pyrolytic exposures. Little chemical change occurred at pyrolysis temperatures of 250 and 300 C, whereas significant mass loss and chemical change was observed at 400 and 500 C. These losses were mainly attributed to evolution of methoxyl, hydroxyl, and propyl groups. Mass loss plateaued following pyrolysis at 500 C, but rearrangements continued to occur at higher temperatures, resulting in char that became increasingly polyaromatic in nature. Following brief pyrolytic exposures at 500 and 600 C, the refined hardwood and softwood lignins yielded coal-like products. Lignin pyrolyzed at higher temperatures yielded chars with greater order, similar in composition to coke. These coal and coke-like products are called "lignin-based carbon" (LBC). The polyaromatic nature of the LBC after high temperature pyrolysis was perceived as the result of radical formation and recombination, leading to fused aromatic structures, which occurs more readily at higher temperatures.
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U2 - 10.1016/j.carbon.2013.04.087
DO - 10.1016/j.carbon.2013.04.087
M3 - Article
AN - SCOPUS:84878592176
SN - 0008-6223
VL - 60
SP - 531
EP - 537
JO - Carbon
JF - Carbon
ER -