基于非等温热重试验的无烟煤与烟煤共燃研究

IF 0.5 Q4 ENGINEERING, CHEMICAL
Xue-peng Mu, Qing-hai Pang, Da-wei Zhang, Chuan-rong Wang, Yi Zhang, Hong-zhuang Gao
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引用次数: 0

摘要

通过非等温热重动力学实验结合傅里叶变换红外光谱分析,系统地阐明了单个煤结构控制混煤燃烧行为的跨尺度机理。选择了三种无烟煤和六种烟煤,根据20%的挥发物阈值设计了梯度混合方案。利用体积模型、未反应核模型和随机孔隙模型对燃烧动力学进行解耦,并辅以扫描电镜对微观结构演化进行表征。结果表明,在250 ~ 450℃之间,脂肪侧链和含氧官能团主导了挥发分的释放,随着短链烷烃比例的增加,混合燃料的热解活化能降低了56%。在450 ~ 700℃的温度范围内,固定碳氧化过程的动力学连续性是由芳香缩合度和碳结构顺序参数之间的协同作用所控制的,通过孔隙拓扑演化和灰层扩散限制来调节。值得注意的是,在无烟煤X与沥青Z配比为1:1的DZX试验组中,芳香族缩合体系中的电子离域导致燃烧曲线左移,达到了680℃的燃尽温度降低,从而证明了官能团的结构互补性,超越了传统混合理论的阈值。通过建立集官能团定向重组、孔隙拓扑演化和燃烧动力学响应为一体的多尺度关联框架,研究了煤分子单元与宏观燃烧性能之间的定量构效关系,为优化工业混煤效率提供了分子相容性驱动的理论基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Investigation on Co-Combustion of Anthracite and Bituminite Based on Non-Isothermal Thermogravimetric Test

Investigation on Co-Combustion of Anthracite and Bituminite Based on Non-Isothermal Thermogravimetric Test

The cross-scale mechanism by which individual coal structures govern blended coal combustion behavior is systematically elucidated through non-isothermal thermogravimetric kinetic experiments integrated with Fourier-transform infrared spectroscopy analysis. Three anthracites and six bituminous coals were selected, with gradient-blending protocols designed based on a 20 wt % volatile matter threshold. Combustion kinetics were decoupled using the volume model, unreacted core model, and random pore model, complemented by scanning electron microscopy to characterize microstructural evolution. Results demonstrate that aliphatic side chains and oxygen-containing functional groups dominated the release of volatile between 250 to 450°C, with pyrolysis activation energy reduced by 56% as short-chain alkane proportions increase in blended fuels. In temperature range between, 450 and 700°C, kinetic continuity during fixed carbon oxidation is governed by synergistic interactions between aromatic condensation degrees and carbon structural order parameters, mediated through pore topology evolution and ash-layer diffusion limitations. Notably, in the DZX experimental group with a 1 : 1 blend ratio of anthracite X and bituminous Z, electron delocalization within aromatic condensation systems induced a leftward shift of combustion profiles, achieving a reduced burnout temperature of 680°C, thereby demonstrating structural complementarity of functional groups that transcends thresholds of traditional blending theories. By establishing a multiscale correlation framework integrating functional group-directed reorganization, pore topology evolution, and combustion kinetic response, this work delineates a quantitative structure-activity relationship between coal molecular units and macroscopic combustion performance, providing a molecular compatibility-driven theoretical foundation for optimizing industrial blended coal efficiency.

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来源期刊
Coke and Chemistry
Coke and Chemistry ENGINEERING, CHEMICAL-
CiteScore
0.70
自引率
50.00%
发文量
36
期刊介绍: The journal publishes scientific developments and applications in the field of coal beneficiation and preparation for coking, coking processes, design of coking ovens and equipment, by-product recovery, automation of technological processes, ecology and economics. It also presents indispensable information on the scientific events devoted to thermal rectification, use of smokeless coal as an energy source, and manufacture of different liquid and solid chemical products.
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