TY - JOUR
T1 - An integrated utilization strategy of printed circuit boards and waste tire by fast co-pyrolysis
T2 - Value-added products recovery and heteroatoms transformation
AU - Ma, Chuan
AU - Kumagai, Shogo
AU - Saito, Yuko
AU - Kameda, Tomohito
AU - Yoshioka, Toshiaki
N1 - Funding Information:
This study was supported by the Japan Society for Promotion of Science (JSPS) KAKENHI (grant numbers: 20F20089 and 19H04306 ) and JST FOREST Program ( JPMJFR206U ). Dr. Chuan Ma would also like to thank JSPS for providing the JSPS standard postdoctoral fellowship for research in Japan.
Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2022/5/15
Y1 - 2022/5/15
N2 - Fast co-pyrolysis has been suggested as a promising technique to solve the environmental issues and simultaneously recover value-added products from polymer wastes. However, to date, no studies have focused on fast co-pyrolysis of printed circuit boards (PCB) and waste tire (WT). Therefore, we comprehensively investigated the fast co-pyrolysis of PCB and WT using pyrolysis-gas chromatography/mass spectrometry. The results show that an increase in temperature during fast pyrolysis improved the interactions between the PCB and WT pyrolyzates, increasing the formation of aliphatic and aromatic compounds. The formation of p-cymene was greatly induced by the isomerization and dehydrogenation reactions of D-limonene. Co-pyrolysis reduced the formation of brominated phenols and benzothiazole from PCB and WT pyrolysis, respectively, whereas promoted the interactions between Br- and S/N-containing radicals, concentrating them into heavy compounds. Increasing the temperature enhanced the release of heteroatom compounds. The findings suggest that debromination of PCB achieved via dehydrogenation of WT pyrolysis provoked secondary reactions of olefins and interactions of heteroatom radicals. The major products were accurately predicted by different fitting models using response surface methodology, indicating the synergistic interactions during co-pyrolysis. The results were beneficial for optimizing the experimental parameters to obtain the maximum yield of desired products.
AB - Fast co-pyrolysis has been suggested as a promising technique to solve the environmental issues and simultaneously recover value-added products from polymer wastes. However, to date, no studies have focused on fast co-pyrolysis of printed circuit boards (PCB) and waste tire (WT). Therefore, we comprehensively investigated the fast co-pyrolysis of PCB and WT using pyrolysis-gas chromatography/mass spectrometry. The results show that an increase in temperature during fast pyrolysis improved the interactions between the PCB and WT pyrolyzates, increasing the formation of aliphatic and aromatic compounds. The formation of p-cymene was greatly induced by the isomerization and dehydrogenation reactions of D-limonene. Co-pyrolysis reduced the formation of brominated phenols and benzothiazole from PCB and WT pyrolysis, respectively, whereas promoted the interactions between Br- and S/N-containing radicals, concentrating them into heavy compounds. Increasing the temperature enhanced the release of heteroatom compounds. The findings suggest that debromination of PCB achieved via dehydrogenation of WT pyrolysis provoked secondary reactions of olefins and interactions of heteroatom radicals. The major products were accurately predicted by different fitting models using response surface methodology, indicating the synergistic interactions during co-pyrolysis. The results were beneficial for optimizing the experimental parameters to obtain the maximum yield of desired products.
KW - Co-pyrolysis
KW - Heteroatom
KW - Printed circuit boards
KW - Product predication
KW - Waste tire
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U2 - 10.1016/j.jhazmat.2022.128420
DO - 10.1016/j.jhazmat.2022.128420
M3 - Article
C2 - 35149505
AN - SCOPUS:85124205717
SN - 0304-3894
VL - 430
JO - Journal of Hazardous Materials
JF - Journal of Hazardous Materials
M1 - 128420
ER -