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Pyrolysis performance, kinetic, thermodynamic, product and joint optimization analyses of incense sticks in N_2 and CO_2 atmospheres

机译:N_2和CO_2气氛下香的热解性能,动力学,热力学,产物和联合优化分析

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摘要

Thermogravimetric and pyrolysis-gas chromatography/mass spectrometry analyses were performed to quantify the pyrolysis performances, kinetics, thermodynamics, products and optimization of incense sticks (IS) in N-2 and CO2 atmospheres at five heating rates. The increased heating rate caused a lagged IS pyrolysis, moving its curves to a higher temperature. According to four model-free methods, activation energy estimates ranged from 34.17 to 439.19 kJ.mol(-1) and 28.46-187.34 kJ.mol(-1) in the N-2 and CO2 atmospheres, respectively. The three-dimension diffusion (spherical symmetry) (D3) was determined using the Horowitz-Metzger method as the most probable degradation mechanism in both atmospheres. The main pyrolytic products were found as benzene and its derivatives whose mass accounted for 49.94% of the total 18 products. Significant two-way interaction effects were found between temperature, heating rate, and atmosphere type on the three responses of remaining mass, derivative thermogravimetry, and differential scanning calorimetry (p = 0.001). The best joint optimization was obtained at 899.5 degrees C with the heating rate of 5 degrees C.min(-1) in the CO2 atmosphere and was more sensitive to the increased heating rate in the N-2 than CO2 atmosphere. (C) 2019 Elsevier Ltd. All rights reserved.
机译:进行了热重分析和热解气相色谱/质谱分析,以量化在五个加热速率下在N-2和CO2气氛下香气棒(IS)的热解性能,动力学,热力学,产物和优化。升高的加热速率导致IS热解反应滞后,从而将其曲线移至更高的温度。根据四种无模型方法,在N-2和CO2大气中,活化能估算值分别为34.17至439.19 kJ.mol(-1)和28.46-187.34 kJ.mol(-1)。使用Horowitz-Metzger方法确定了二维扩散(球形对称)(D3),这是两种大气中最可能的降解机理。发现主要的热解产物为苯及其衍生物,其质量占全部18种产物的49.94%。发现温度,加热速率和气氛类型对剩余质量,导数热重分析和差示扫描量热法的三个响应之间存在显着的双向相互作用效应(p = 0.001)。在899.5摄氏度下,CO2气氛中的加热速率为5℃.min(-1)可获得最佳的接头优化,并且对N-2中升高的加热速率比CO2气氛更敏感。 (C)2019 Elsevier Ltd.保留所有权利。

著录项

  • 来源
    《Renewable energy》 |2019年第10期|814-827|共14页
  • 作者单位

    Guangdong Univ Technol, Guangzhou Key Lab Environm Catalysis & Pollut Con, Guangdong Key Lab Environm Catalysis & Hlth Risk, Sch Environm Sci & Engn,Inst Environm Hlth & Poll, Guangzhou 510006, Guangdong, Peoples R China;

    Guangdong Univ Technol, Guangzhou Key Lab Environm Catalysis & Pollut Con, Guangdong Key Lab Environm Catalysis & Hlth Risk, Sch Environm Sci & Engn,Inst Environm Hlth & Poll, Guangzhou 510006, Guangdong, Peoples R China;

    Guangdong Univ Technol, Guangzhou Key Lab Environm Catalysis & Pollut Con, Guangdong Key Lab Environm Catalysis & Hlth Risk, Sch Environm Sci & Engn,Inst Environm Hlth & Poll, Guangzhou 510006, Guangdong, Peoples R China;

    Abant Izzet Baysal Univ, Dept Chem Engn, TR-14052 Bolu, Turkey;

    Abant Izzet Baysal Univ, Dept Environm Engn, TR-14052 Bolu, Turkey|Ardahan Univ, Dept Environm Engn, TR-75002 Ardahan, Turkey;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Joint optimization; Thermogravimetric analysis; Py-GC/MS; Degradation mechanism; Model-free methods;

    机译:联合优化;热重分析;Py-GC / MS;降解机理;无模型方法;

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