TY - JOUR
T1 - Virtuous utilization of carbon dioxide in pyrolysis of polylactic acid
AU - Cho, Seong Heon
AU - Kim, Youkwan
AU - Lee, Sangyoon
AU - Andrew Lin, Kun Yi
AU - Chen, Wei Hsin
AU - Jung, Sungyup
AU - Lee, Doyeon
AU - Hyun Moon, Deok
AU - Jeon, Young Jae
AU - Kwon, Eilhann E.
N1 - Funding Information:
This study was supported by a National Research Foundation of Korea (NRF) grant funded by the Korean government (MSIT) (No. NRF-2021R1A6A3A13044307; 2021R1F1A1052782). Seong-Heon Cho also acknowledges the financial support from the Hyundai Motor Chung Mong-Koo Foundation. This research was also supported by Korea Electric Power (Grant Number: R19XO02-01).
Publisher Copyright:
© 2023 Elsevier B.V.
PY - 2023/6/15
Y1 - 2023/6/15
N2 - Polylactic acid has been adopted as a strategic alternative to petroplastics because of its biodegradability. The waste generation rate could be proportional to its use, considering the short lifespan of polylactic acid. However, a practical disposal or recycling protocol for polylactic acid waste has not yet been developed. Thus, this study suggests a promising thermochemical platform for valorizing polylactic acid waste into energy resources (syngas). Specifically, carbon dioxide-assisted pyrolysis has been suggested to impart environmental features to polylactic acid disposal. Before the pyrolysis tests, the polylactic acid waste sample was characterized by Fourier transform-infrared spectrometer and thermogravimetric analyses, which showed that polylactic acid contained a substantial amount of additives and impurities (∼13 wt%). The impurity containing polylactic acid was converted into pyrogenic gases and biocrudes through pyrolysis process. The pyrolysis was performed under carbon dioxide condition and led to enhanced carbon monoxide formation from simultaneous homogeneous reactions between CO2 and volatile organic compounds evolved from thermal degradation of polylactic acid. CO2 was reduced and the volatile compounds were oxidized. The evolution of carbon monoxide from pyrolysis under carbon dioxide condition was 2 times higher than that from nitrogen condition. The concentration of carbon monoxide from the pyrolysis of polylactic acid waste with respect to plastics and biomass was considerably higher. This observation indicates that the susceptibility of carbon dioxide to the homogeneous reaction is highly sensitive. To seek a way to hasten the homogeneous reaction, silica supported nickel catalysts were applied. The evolution of carbon monoxide from catalytic pyrolysis under carbon dioxide condition was 4.5 times higher than inert atmosphere.
AB - Polylactic acid has been adopted as a strategic alternative to petroplastics because of its biodegradability. The waste generation rate could be proportional to its use, considering the short lifespan of polylactic acid. However, a practical disposal or recycling protocol for polylactic acid waste has not yet been developed. Thus, this study suggests a promising thermochemical platform for valorizing polylactic acid waste into energy resources (syngas). Specifically, carbon dioxide-assisted pyrolysis has been suggested to impart environmental features to polylactic acid disposal. Before the pyrolysis tests, the polylactic acid waste sample was characterized by Fourier transform-infrared spectrometer and thermogravimetric analyses, which showed that polylactic acid contained a substantial amount of additives and impurities (∼13 wt%). The impurity containing polylactic acid was converted into pyrogenic gases and biocrudes through pyrolysis process. The pyrolysis was performed under carbon dioxide condition and led to enhanced carbon monoxide formation from simultaneous homogeneous reactions between CO2 and volatile organic compounds evolved from thermal degradation of polylactic acid. CO2 was reduced and the volatile compounds were oxidized. The evolution of carbon monoxide from pyrolysis under carbon dioxide condition was 2 times higher than that from nitrogen condition. The concentration of carbon monoxide from the pyrolysis of polylactic acid waste with respect to plastics and biomass was considerably higher. This observation indicates that the susceptibility of carbon dioxide to the homogeneous reaction is highly sensitive. To seek a way to hasten the homogeneous reaction, silica supported nickel catalysts were applied. The evolution of carbon monoxide from catalytic pyrolysis under carbon dioxide condition was 4.5 times higher than inert atmosphere.
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U2 - 10.1016/j.cej.2023.143307
DO - 10.1016/j.cej.2023.143307
M3 - Article
AN - SCOPUS:85154567958
SN - 1385-8947
VL - 466
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 143307
ER -