Impact of plastic type on synergistic effects during co-pyrolysis of rice husk and plastics

烧焦 热解 去壳 化学 聚丙烯 化学工程 聚合物 有机化学 聚乙烯 聚对苯二甲酸乙二醇酯 聚苯乙烯 高分子化学 核化学 材料科学 复合材料 植物 生物 工程类
作者
Engamba Esso Samy Berthold,Wei Deng,Junbo Zhou,A Bertrand,Jun Xu,Long Jiang,Sheng Su,Song Hu,Xun Hu,Yi Wang,Jun Xiang
出处
期刊:Energy [Elsevier BV]
卷期号:281: 128270-128270 被引量:27
标识
DOI:10.1016/j.energy.2023.128270
摘要

Pyrolysis of varied type of plastic waste generates distinct reaction intermediates, which affect their co-pyrolysis with biomass feedstock in different ways. This was investigated herein in co-pyrolysis of specific plastic types, including polypropylene (PP), polystyrene (PS), polyethylene terephthalate (PET), and polycarbonate (PC), as well as rice husk (RH) at 600–800 °C. The experimental results demonstrated that synergistic mechanisms in the co-pyrolysis were dependent on plastic type. PP provided small hydrogen radicals to pyrolyzates derived from RH, leading to an increase in aromatic production up to 69.5% at 600 °C. PS melted and acted as an insulator, inhibiting oil formation while increasing char yield. Organic acids derived from PET enhanced the char formation and dehydration of RH, resulting in increased levels of char and water. The interaction between RH/PET resulted in a reduction of aromatics by 53.2% at 800 °C because of the synergistic promotion of water formation. In contrast, aromatic structures in PC interfered with degradation of oxygen-containing functional groups in RH, enhancing oil, with aromatics increasing by 35.7% at 700 °C, as well as increased gas yields through promoting decomposition of RH. Furthermore, when all the feedstocks were mixed together, accelerated pyrolytic interactions enhanced the cracking of each individual polymer.
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