Novel insights into mass transfer-controlled radical-mediated co-pyrolysis of lignin with typical plastics

木质素 化学 电子顺磁共振 激进的 纤维素 有机化学 热解 烧焦 化学工程 高分子化学 核磁共振 物理 工程类
作者
Yuyang Fan,Chao Liu,Zhengxue Zhang,Jia Ouyang,Fuli Deng,Ruixue Zhao,Huiyan Zhang,Rui Xiao
出处
期刊:Chemical Engineering Journal [Elsevier]
卷期号:480: 148150-148150 被引量:2
标识
DOI:10.1016/j.cej.2023.148150
摘要

Co-pyrolysis of lignin with representative waste plastics, including polypropylene (PP), acrylonitrile butadiene styrene (ABS), polystyrene (PS), and polyethylene terephthalate (PET), was investigated, focusing on radical-mediated reactions, with radical detection via electron paramagnetic resonance (EPR). During the co-pyrolysis of lignin with PP, favorable synergistic effects were observed, resulting in a significant 17 % enhancement in phenolic compound yields within the fixed-bed reactor, whereas the presence of other plastics led to exacerbated cross-linking carbonization in contrast. Furthermore, TOF-MS and FT-ICR-MS analyses corroborated that the bio-oil derived from lignin/PP exhibited a higher phenolic content and lower carbon number distribution. Additionally, the radical concentrations in bio-oil of lignin/PP were determined to be the lowest (1.07 × 1013 spins/µL), providing compelling evidence of the strong interaction between lignin and PP. Interestingly, EPR spectroscopy detected the resultant lowest spin concentrations (1.28 × 1019 spins/g) in lignin/PP char, in contrast to lignin in isolation or within other plastics, which strongly indicating that hydrogen-rich radicals originating from PP were responsible for inducing more effective quenching reactions with lignin intermediates. Moreover, the lignin/PP char demonstrated the highest carbon content (80.30 %) and the lowest ID/IG ratio (1.98), further affirming a highly effective interaction between lignin and PP. The perspective drawn from this study is that the abundant hydrogen source of PP can provide hydrogen-rich radicals to quench lignin intermediates and improve phenolic yield. This intriguing work provides a fresh perspective to evaluate the effect of plastic origin on lignin co-pyrolysis based on radical theory.
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