This paper reports the mineralogy and geochemistry of the Late Permian C1 Coal from Bole and Laibin mines in eastern Yunnan, Southwestern China (C1 Coal in Laibin mine is composed of three layers termed B1, B2, and B3). The coals are characterized by medium-high ash yields and very low sulfur contents. Compared with average values of trace element concentrations in hard coals worldwide, the Bole and Laibin coals are enriched in V, Co, Cu, Zn, and Se, which were mainly derived from the sediment-source region of the Kangdian Upland. Major minerals in the coal samples and roof and floor strata include quartz, interstratified berthierine/chamosite (B/C), as well as kaolinite, mixed layer illite/smectite, calcite, pyrite, and anatase. Unlike a pure chamosite, the 7 Å peak of interstratified B/C is sharp and narrow, while the 14 Å peak is broad and weak, or absent in some coal samples. Interstratified B/C was largely precipitated from low-temperature Fe-rich and Mg-rich hydrothermal fluids or, in some cases, is an alteration product of kaolinite. Secondary phases of quartz, calcite, pyrite, kaolinite, chalcopyrite, gypsum, and REE-phosphates in the coal samples are the dominant authigenic minerals formed at syngenetic and early diagenetic stages. Four intra-seam partings in C1 Coal, B1, and B3 layers are identified as tonsteins derived from felsic volcanic ashes. These tonsteins consist mainly of cryptocrystalline kaolinite with graupen and vermicular textures, and minor amounts of high-temperature quartz, zircon, apatite, monazite, and anatase. The floor of the C1 Coal in the Bole mine is a tuffaceous claystone and consists of altered high-Ti basalt volcaniclastics, characterized by high concentrations of Zr, Nb, V, Co, Cu, and Zn, low Al₂O₃/TiO₂ ratio (~4.62), high Ti/Y ratio (~900), enrichment of middle rare earth elements, and positive Eu anomalies.

Nanoscale pore structure characteristics and their main controlling factors are key elements affecting the gas storage capacity, permeability, and the accumulation mechanism of shale. A multidisciplinary analytical program was applied to quantify the pore structure of all sizes of Xiamaling shale from Zhangjiakou, Hebei. The result implies that Mercury injection porosimetry (MIP) and low-pressure N₂ curves of the samples can be divided into three and four types, respectively, reflecting different connectivity performances. The maximum CO₂ adsorbing capacity increases with increasing total organic carbon (TOC) content, pore volume (PV), and surface area (SA) of the micropores are distributed in a three-peak type. The full-scale pore structure distribution characteristics reveal the coexistence of multiple peaks with multiple dominant scales and bi-peak forms with mesopores and micropores. The porosity positively correlates with the TOC and quartz content, but negatively correlates with clay mineral content. Organic matter (OM) is the main contributor to micropore and mesopore development. Smectite and illite/smectite (I/S) assist the development of the PV and SA of pores with different size. Illite promotes the development of the nanoscale PV, but is detrimental to the development of the SA. Thermal maturity controls the evolution of pores with different size, and the evolution model for the TOC-normalized PVs of different diameter scales is established. Residual hydrocarbon is mainly accumulated in micropores sized 0.3 to 1.0 nm and mesopores sized 40 nm, 2 nm and less than 10 nm. Since the samples were extracted, the pore space occupied by residual hydrocarbon was released, resulting in a remarkable increase in PV and SA.

The modes of occurrence, migration, and evolution pathways of lithium (Li) and gallium (Ga) during combustion of an Al-rich coal from Inner Mongolia, China, were investigated using methods of simulated combustion experiments, the sequential chemical extraction procedure (SCEP), and the thermodynamic equilibrium calculation. Mineralogical and chemical compositions of the feed coal and combustion ash were analyzed by X-ray fluorescence (XRF), X-ray diffraction (XRD), inductively coupled plasma mass spectrometry (ICP-MS), and scanning electron microscopy (SEM). The study reveals that Li and Ga are significantly enriched in the ash after combustion, with the contents reaching up to 1086 μg/g and 133 μg/g, respectively. The primary modes of occurrence of Li and Ga in the ash are quartz and aluminosilicates, and sulfides, respectively. Li, in the form of LiAlSi₄O₁₀ (s), primarily occurs in hematite, glass, and quartz below 800 °C. However, it migrates into the glass phase, mullite, and quartz above 1000 °C. On the other hand, Ga exists as Ga₄S₅ (s) and transforms into Ga₂S (g) as the temperature rises from 800 °C to 1000 °C, maintaining this gaseous form until 1200 °C. Ga₄S₅ (s) predominantly occurs in the glass phase at 600 °C, whereas mullite and quartz become its dominant modes of occurrence in industrial combustion ashes and ashes obtained from simulated combustion above 600 °C.