热解
生物炭
热重分析
聚乙烯
聚氯乙烯
聚苯乙烯
聚丙烯
聚对苯二甲酸乙二醇酯
傅里叶变换红外光谱
材料科学
核化学
化学工程
残留物(化学)
化学
有机化学
复合材料
聚合物
工程类
作者
Rongjie Chen,Shiyu Zhang,Xiaoxiao Yang,Guanghao Li,Hui Zhou,Qinghai Li,Yanguo Zhang
标识
DOI:10.1016/j.wasman.2021.03.001
摘要
The coexistence of plastics and microalgae in the ocean has brought great challenges to the environment. Therefore, co-pyrolysis of microalgae Dunaliella salina (DS) and typical plastics (polypropylene (PP), polystyrene (PS), polyethylene terephthalate (PET), and polyvinyl chloride (PVC)) were investigated using thermogravimetric analyzer with Fourier transform infrared spectrometer. The results showed that the coating effect of the molten plastics promoted the pyrolysis of DS. The solid residue amounts of DS-PP, DS-PS, and DS-PET blends were reduced by 1.55 wt%, 1.39 wt%, 1.69 wt%, respectively, as a result of the hydrogenation reaction between the unsaturated products generated by plastics and biochar. While for DS-PVC, attributed to the physical and chemical effects during the co-pyrolysis process, the solid residue was increased by 1.36 wt%. For the other three blends, the solid residues were reduced due to the hydrogenation reaction between the unsaturated products generated by plastics and biochar. FTIR analysis of gaseous products indicated the total CO2 production increased significantly for DS-PET. Besides, the alkyls generated by DS reacted with HCl during DS-PVC co-pyrolysis, the resulting products were then fixed in biochar. Kinetic results suggested that due to the co-pyrolysis with DS, the activation energies of PP, PS, and PET were reduced by 1/2, 1/3, and 3/4, respectively, and this value for PVC in its second stage was reduced by 1/4. Our results indicated the advantage to co-pyrolyze the microalgae and marine plastics.
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