贺兴处, 陈德珍. 典型聚乙烯、聚丙烯、聚苯乙烯废塑料共热解初期反应特性的ReaxFF分子模拟研究[J]. 燃料化学学报(中英文), 2022, 50(3): 346-356. DOI: 10.1016/S1872-5813(21)60161-5
引用本文: 贺兴处, 陈德珍. 典型聚乙烯、聚丙烯、聚苯乙烯废塑料共热解初期反应特性的ReaxFF分子模拟研究[J]. 燃料化学学报(中英文), 2022, 50(3): 346-356. DOI: 10.1016/S1872-5813(21)60161-5
HE Xing-chu, CHEN De-zhen. ReaxFF MD study on the early stage co-pyrolysis of mixed PE/PP/PS plastic waste[J]. Journal of Fuel Chemistry and Technology, 2022, 50(3): 346-356. DOI: 10.1016/S1872-5813(21)60161-5
Citation: HE Xing-chu, CHEN De-zhen. ReaxFF MD study on the early stage co-pyrolysis of mixed PE/PP/PS plastic waste[J]. Journal of Fuel Chemistry and Technology, 2022, 50(3): 346-356. DOI: 10.1016/S1872-5813(21)60161-5

典型聚乙烯、聚丙烯、聚苯乙烯废塑料共热解初期反应特性的ReaxFF分子模拟研究

ReaxFF MD study on the early stage co-pyrolysis of mixed PE/PP/PS plastic waste

  • 摘要: 利用反应力场分子模拟(ReaxFF MD)结合反应机理自分析(AutoRMA)工具,从动力学、热解产物及热解反应过程三方面在原子层面上,探究了典型聚乙烯(PE)、聚丙烯(PP)、聚苯乙烯(PS)废塑料共热解的反应机理。结果表明,PE/PP/PS共热解的动力学参数可通过C–C键和C–H键断裂的活化能加权求和(即Char Bonds方法) 获得,其活化能估计值与实验值的误差仅为±3.86%;因此可以由C–C键和C–H键的断裂来表征热解反应进程。对于PP-PE混合塑料热解体系,增加其中PP的含量可以提高油和可燃气的产率,而对于PP-PS体系,增加其中PS的含量可以提高炭和油产率。在PE-PP-PS混合塑料热解体系中,高温有利于重油裂解为轻油,轻油相对含量从2400 K的44.77%升高到3000 K的56.18%;同时,高温也会促使烃类小分子进一步裂解生成更小分子产物,随热解温度升高,H2和CH4的产率明显上升,但C2H4和C3H6的产率先上升后降低。相比单独热解,混合热解体系开始反应时间有所延迟,但达到第一次平衡的总反应时间缩短,并且更倾向于生成较小分子的产物。PE和PP单独热解时,首先生成其单体,继而生成烷烃和小分子气体,但在共热解过程中,首先生成烷烃和小分子气体,而后生成其单体。PS在共热解体系中更倾向于提供·H自由基从而与PE和PP生成的自由基结合,形成小分子烷烃或H2

     

    Abstract: The early stage co-pyrolysis of typical plastic waste including polyethylene (PE), polypropylene (PP) and polystyrene (PS) were investigated by using the reactive force field molecular dynamics (ReaxFF MD) simulation with an automatic reaction mechanism analysis software (AutoRMA); the kinetic model, product yields and reaction process of co-pyrolysis were analyzed at atomic level. The results show that the kinetic parameters of PE/PP/PS co-pyrolysis can be obtained through the weighted sum of the parameters for the fracture of C–C and C–H bonds; the estimated activation energy is very close to the experimental one with a small error of ±3.86%, indicating that the fracture of C–C and C–H bonds can accurately characterize the co-pyrolysis process. For the co-pyrolysis of PE-PP mixture, an increase of PP content can improve the yields of oil and combustible gas, whereas for the co-pyrolysis of PP-PS mixture, the increase of PS content can improve the yields of tar and oil. In contrast, for the co-pyrolysis of PE-PP-PS mixture, a higher temperature is beneficial for the conversion of heavy oil into light oil; the light oil content increases from 44.77% at 2400 K to 56.18% at 3000 K. In addition, as a higher temperature can promote the further cracking of light hydrocarbons into gas products of smaller molecules, the yields of H2 and CH4 increase significantly with the increase of pyrolysis temperature, whereas the yields of C2H4 and C3H6 increase first and then decrease with the temperature. In comparison with the separated pyrolysis, the co-pyrolysis commences later, but displays shorter time to reach the first equilibrium state and generates products with smaller molecules. For the separate pyrolysis of PE and PP, their monomers emerge first, hereafter the alkanes and small molecule gases are produced; for the co-pyrolysis process, in contrast, the alkanes and small molecule gases are generated prior to the monomers. Moreover, PS tends to provide ·H radicals in the co-pyrolysis process, which can combine with the free radicals generated from PE and PP pyrolysis, forming small molecule alkanes and H2.

     

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