Comprehensive valorization of oil-rich food waste through coupling transesterification with pyrolysis

被引:0
|
作者
Park, Gyeongnam [1 ]
Lee, Taewoo [1 ]
Kim, Jung-Hun [1 ]
Song, Hocheol [1 ]
Chen, Wei-Hsin [2 ,3 ,4 ]
Kwon, Eilhann E. [1 ]
机构
[1] Hanyang Univ, Dept Earth Resources & Environm Engn, Seoul 04763, South Korea
[2] Natl Cheng Kung Univ, Dept Aeronaut & Astronaut, Tainan 701, Taiwan
[3] Tunghai Univ, Res Ctr Smart Sustainable Circular Econ, Taichung 407, Taiwan
[4] Natl Chin Yi Univ Technol, Dept Mech Engn, Taichung 411, Taiwan
基金
新加坡国家研究基金会;
关键词
Waste valorization; Transesterification; Biodiesel; Catalytic pyrolysis; CO2; utilization; BIODIESEL PRODUCTION; CATALYST; ACID; FAT;
D O I
10.1016/j.jaap.2025.107082
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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-debrisextracted 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 x 108 kg CO2 in South Korea.
引用
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页数:12
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