Evolution of macromolecular structure during coal oxidation via FTIR, XRD and Raman

IF 7.2 2区 工程技术 Q1 CHEMISTRY, APPLIED Fuel Processing Technology Pub Date : 2024-07-31 DOI:10.1016/j.fuproc.2024.108114
Fei Gao , Zhe Jia , Zheng Cui , Ying-di Li , Hao Jiang
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Abstract

The analysis of the macromolecular structure and morphology in coal during oxidation is the basis to explore the mechanism of spontaneous combustion. To explore the evolutionary rules of coal macromolecular structure during oxidation, Fourier Transform Infrared Spectroscopy (FTIR), X-ray Diffraction (XRD), and Raman Spectroscopy (Raman) were employed to analyze the coal samples with different oxidation degrees. The results revealed that the oxidation action led to the decrease of the aliphatic structures and aromatic hydroxyl groups in coal, while promoting the formation of oxygen-containing functional groups and aromatic structures. It also led to a relative increase of free hydroxyl groups linked to hydrogen bonds. The aromatic layer spacing (d002) decreased with increasing oxidation degree, while the microcrystal stacking height (Lc), the aromatic layer diameter (La), the average number of crystal stacking layers (n) generally increased. It indicated that small aromatic ring molecules in coal could undergo continuous polymerization during oxidation to form a single aromatic layer structure. The variation of Raman spectrum parameters exhibited a consistent decreasing trend in WD/WG, ID/IG, AD/AG, and A(GR+SL)/AG value, indicating an increase in the vibration of sp2 hybridization carbon atoms within the lattice structure of coal. Conversely, PG-D, AS/AD and A(GR+VL+VR)/AD value increased overall, suggesting that small aromatic rings decreased in content during oxidation while polymerizing into larger aromatic rings. The coal structure underwent a brief stage of disordered evolution during oxidation, followed by removal of impurity structures and condensation of aromatic structures due to increasing oxidation temperatures, ultimately leading to a highly ordered crystalline state. The oxidation process significantly influenced the development of coal's aromatic structure, particularly in less metamorphic coal. The research findings provide a theoretical basis for analyzing the underlying mechanism behind spontaneous combustion induced by coal oxidation.

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通过傅立叶变换红外光谱、X 射线衍射和拉曼光谱观察煤氧化过程中大分子结构的演变
分析煤在氧化过程中的大分子结构和形态是探索自燃机理的基础。为探索氧化过程中煤炭大分子结构的演化规律,采用傅立叶变换红外光谱法、X射线衍射法和拉曼光谱法对不同氧化程度的煤样进行了分析。结果表明,氧化作用导致煤中脂肪族结构和芳香羟基的减少,同时促进了含氧官能团和芳香结构的形成。氧化作用还导致与氢键相连的游离羟基相对增加。随着氧化度的增加,芳香层间距(d)减小,而微晶堆积高度(L)、芳香层直径(L)、平均晶体堆积层数(n)普遍增加。这表明煤中的小芳香环分子在氧化过程中可以发生连续聚合,形成单层芳香层结构。拉曼光谱参数的变化在 W/W、I/I A/A 和 A/A 值上表现出一致的下降趋势,表明煤晶格结构中 sp 杂化碳原子的振动增加。相反,P、A/A 和 A/A 值则整体上升,表明在氧化过程中,小芳香环的含量减少,同时聚合成较大的芳香环。煤的结构在氧化过程中经历了短暂的无序演化阶段,随后随着氧化温度的升高,杂质结构被去除,芳香结构凝结,最终形成高度有序的结晶状态。氧化过程极大地影响了煤的芳香结构的发展,尤其是在变质程度较低的煤中。这些研究成果为分析煤氧化诱发自燃的内在机理提供了理论依据。
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来源期刊
Fuel Processing Technology
Fuel Processing Technology 工程技术-工程:化工
CiteScore
13.20
自引率
9.30%
发文量
398
审稿时长
26 days
期刊介绍: Fuel Processing Technology (FPT) deals with the scientific and technological aspects of converting fossil and renewable resources to clean fuels, value-added chemicals, fuel-related advanced carbon materials and by-products. In addition to the traditional non-nuclear fossil fuels, biomass and wastes, papers on the integration of renewables such as solar and wind energy and energy storage into the fuel processing processes, as well as papers on the production and conversion of non-carbon-containing fuels such as hydrogen and ammonia, are also welcome. While chemical conversion is emphasized, papers on advanced physical conversion processes are also considered for publication in FPT. Papers on the fundamental aspects of fuel structure and properties will also be considered.
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