4.7 Article

Mechanism of carbon structure transformation in plastic layer and semi-coke during coking of Australian metallurgical coals

Journal

FUEL
Volume 315, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.fuel.2022.123205

Keywords

Coking process; Crosslinking structures; Plastic layer; Semi-coke; Radical formation

Funding

  1. Australian Coal Industry's Research Program (ACARP) [C28064, C33059]
  2. National Natural Science Foundation of China [22078141]
  3. Foundation of State Key Laboratory of Coal Conversion [J20-21-301]
  4. University of Newcastle

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This study investigated the impact of parent coal properties on the evolution of carbon structures during the coking process. The results showed that coal undergoes crosslinking reactions, condensation, and re-polymerization, forming carbon-bearing crosslinking structures. Higher rank coals produced more stable radicals in the plastic phase, while lower rank coals formed oxygen-bearing cross-links at early plastic stages.
The transformation of the carbon structure of coal during the coking process influences the coke microstructure and microtexture, and ultimately, the coke quality. This study investigates the impacts of parent coal properties on the evolution of carbon structures of selected Australian coals from the plastic layer to semi-coke stage during coking using electron spin resonance (ESR), Synchrotron attenuated total reflection Fourier transform infrared microspectmscopy (Synchrotron ATR-FTIR) and solid-state carbon-13 nuclear magnetic resonance (C-13 NMR) analyses. The stable radical concentration, the g-value, and the linewidth measured by ESR were combined with IR and Solid-state C-13 NMR results to improve the understanding of carbon structural transformation at the plastic and post-resolidification stages of coke formation. In addition, micro gas chromatography (micro-GC) was used to study the evolution of gaseous species. The results suggested that the coal undergoes crosslinking reaction, condensation, and re-polymerization within the thermoplastic range, resulting in loss of oxygen to form condensed carbon-bearing crosslinking structures. Due to differences in their chemical structure, macerals significantly influenced crosslinking structures during plastic layer formation. Higher rank coals generated more stable radicals in the plastic phase due to their lower H/C and O/C ratios than low-rank coals with higher vitrinite contents. Lower fluidity and lower rank coals formed oxygen-bearing cross-links at the early plastic stages, hindering fluidity development and carbon ordering at high temperatures. Above the resolidification point, the continuous transformation of C-O and C-H bonds to C-C bonds was accompanied by the release of H-2 and CO2, leading to increased ordering and anisotropy of coke carbon structures.

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