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Pyrolysis Characteristics of Low-Rank Coal under a CO-Containing Atmosphere and Properties of the Prepared Coal Chars

机译:含CO气氛下低阶煤的热解特性及制得的煤焦性质

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摘要

Herein, the pyrolysis characteristics of low-rank coal under a CO-containing atmosphere was studied via thermogravimetry coupled with mass spectrometry and Fourier transform infrared analysis. Further, the pore structure, carbon chemical structure, and combustion reactivity of the prepared coal chars were characterized via N-2/CO2 adsorption, Raman spectroscopy, and thermal analysis, respectively. The CO-containing atmosphere suppressed coal devolatilization at the rapid pyrolysis stage. During coal pyrolysis, this atmosphere reduced CH4 evolution by suppressing the formation of free radicals such as CH3 center dot and CH2 center dot; H-2 evolution reduced owing to the inhibition of the formation of hydrogen free radicals and the working of the inverse water-gas reaction; the H2O yield was increased through the inverse water-gas reaction but not by the conversion of the hydroxyl group in coal. At 300-700 degrees C, the disproportionation reaction of CO produced copious CO2 molecules, significantly raising the CO2 emission intensity over the CO2 released during coal pyrolysis. The pore structure of the chars-CO was suppressed via shingling of the carbon particles generated in the disproportionation reaction and the inverse water-gas reaction, which inhibits the release of volatiles in a CO-containing atmosphere. The carbon chemical structure of the chars-CO was ordered by the interaction between the char's skeleton structure and the newly formed carbon and the contribution of the carbon particles with an ordered structure adhered on the char. The combustion reactivity of chars-CO was not improved by its higher volatile content, because the underdeveloped pore structure and ordered carbon structure degraded the combustion reactivity of chars-CO. Conversely, the pore structure of chars-CO is more developed than that of chars-N-2 due to the release of volatiles in the high-temperature segment before the gasification reaction starts so as to improve the gasification reactivity of chars-CO.
机译:在此,通过热重分析,质谱分析和傅立叶变换红外分析,研究了低阶煤在含CO气氛下的热解特性。此外,分别通过N-2 / CO2吸附,拉曼光谱和热分析对制得的煤焦的孔结构,碳化学结构和燃烧反应性进行了表征。含CO的气氛在快速热解阶段抑制了煤的挥发。在煤热解过程中,这种气氛通过抑制自由基的形成(如CH3中心点和CH2中心点)减少了CH4的释放。由于抑制了氢自由基的形成和水煤气逆反应的进行,H-2的析出减少。 H2O的收率是通过逆水煤气反应而增加的,而不是通过煤中羟基的转化而增加的。在300-700摄氏度下,CO歧化反应产生大量的CO2分子,大大提高了煤热解过程中释放的CO2的排放强度。通过歧化反应和逆水煤气反应中生成的碳颗粒的混叠,抑制了焦炭-CO的孔结构,从而抑制了在含CO的气氛中挥发物的释放。炭-CO的碳化学结构是通过炭的骨架结构与新形成的碳之间的相互作用以及附着在炭上的具有有序结构的碳颗粒的贡献而有序的。焦炭-CO的燃烧反应性没有因为其较高的挥发物含量而得到改善,因为孔结构和碳结构的不发达降低了焦炭-CO的燃烧反应性。相反,由于在气化反应开始之前高温段中挥发物的释放,使得chars-CO的孔结构比chars-N-2的孔结构更发达,从而提高了chars-CO的气化反应性。

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  • 来源
    《Energy & fuels》 |2019年第7期|6098-6112|共15页
  • 作者单位

    Xian Univ Architecture & Technol, Sch Met Engn, Xian 710311, Shaanxi, Peoples R China;

    Xian Univ Architecture & Technol, Sch Met Engn, Xian 710311, Shaanxi, Peoples R China;

    Xian Univ Architecture & Technol, Sch Met Engn, Xian 710311, Shaanxi, Peoples R China;

    Xian Univ Architecture & Technol, Sch Met Engn, Xian 710311, Shaanxi, Peoples R China;

    Xian Univ Architecture & Technol, Sch Met Engn, Xian 710311, Shaanxi, Peoples R China;

    Xian Univ Architecture & Technol, Sch Met Engn, Xian 710311, Shaanxi, Peoples R China;

    Xian Univ Architecture & Technol, Sch Met Engn, Xian 710311, Shaanxi, Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
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  • 正文语种 eng
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