Comprehensive valorization of oil-rich food waste through coupling transesterification with pyrolysis
- Authors
- Park, Gyeongnam; Lee, Taewoo; Kim, Jung-Hun; Song, Hocheol; Chen, Wei-Hsin; Kwon, Eilhann E.
- Issue Date
- Aug-2025
- Publisher
- Elsevier BV
- Keywords
- Waste valorization; Transesterification; Biodiesel; Catalytic pyrolysis; CO2 utilization
- Citation
- Journal of Analytical and Applied Pyrolysis, v.189, pp 1 - 12
- Pages
- 12
- Indexed
- SCIE
SCOPUS
- Journal Title
- Journal of Analytical and Applied Pyrolysis
- Volume
- 189
- Start Page
- 1
- End Page
- 12
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/206845
- DOI
- 10.1016/j.jaap.2025.107082
- ISSN
- 0165-2370
1873-250X
- Abstract
- Recent shifts in food consumption trends toward fried foods have increased the generation of oil-rich food waste. Although biological processes show promise for the food waste valorization, the presence of oil components limits microbial activity. This study proposes a thermochemical approach for valorizing oil-rich fried debris, a by-product of deep-frying, by coupling transesterification with pyrolysis. Characterization of fried-debris-extracted oil (FDO) revealed high impurity levels, free fatty acids and aldehydes. This necessitates transesterification method with more tolerance to these impurities than the conventional acid-treated process. A thermally-induced transesterification demonstrated the impurity tolerance, representing biodiesel yield exceeding 95 wt% regardless of the mixing ratio of aldehyde-to-refined olive oil. When applying to FDO, this process yielded a consistent biodiesel output (41.1 wt%), representing a 1.43-fold increase compared with the conventional transesterification. As a strategy for the comprehensive valorization of fried debris, de-fatted fried debris (DFD) remaining after oil extraction was further pyrolyzed. To impart a sustainability to the pyrolysis system, CO2 was employed as a reactive agent. CO2 showed a reactivity of converting DFD-derived volatiles into syngas, particularly CO, while producing biochar. The CO2 reactivity was accelerated when conducting catalytic pyrolysis over Ni catalyst, resulting in 71.43 wt% syngas and 18.47 wt% biochar. To evaluate the environmental benefits of this process, the CO2 mitigation potential of biodiesel, syngas, and biochar was estimated, representing an annual reduction of 14.24 × 108 kg CO2 in South Korea.
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Collections - 서울 공과대학 > 서울 자원환경공학과 > 1. Journal Articles

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