The coal structure is extensively used for studying the properties of coal, and the construction of accurate and reliable coal structure models can promote these researches. In this study, Fourier transform infrared (FTIR) spectroscopy and X-ray diffraction (XRD) were used to analyze the changes in the coal structure as a function of the coalification degree, and a semiquantitative model construction method based on FTIR, XRD, and X-ray photoelectron spectroscopy (XPS) analyses was proposed. With an increase in the coalification degree, the size of the aromatic cores in the coal increased. During the conversion from lignite to bituminous coal, the content of aliphatic structures increased, while the content of oxygen-containing functional groups (OFGs) significantly decreased. Conversely, during the conversion from bituminous coal to anthracite, the content of aliphatic structures decreased while the content of OFGs slightly increased. The calculated FTIR spectra of the coal structure models were consistent with the experimental FTIR spectra, which confirmed the accuracy of the models. Furthermore, the models successfully explained the microscopic mechanism underlying the differences in the wettability of the coal samples with varying coalification degrees. The construction method and coal structure models in this study will be more widely applied in future research.

The problem of low-rank coal flotation continues to be a challenge due to the poor hydrophobicity and abundant oxygenated functional groups on particle surfaces. In this study, carrier flotation was used to improve the flotation performance of low-rank coal with polystyrene as a carrier material. Kerosene was used as a collector and played a role in the adhesion of fine low-rank coal to polystyrene due to its hydrophobic properties. The carrier feature of polystyrene was demonstrated by Turbiscan Lab Expert stability analysis and scanning electron microscopy analysis. The flotation experiments revealed that the optimum conditions were: collector dosage 5000 g/t, pulp concentration 40 g/L, and the ratio of low-rank coal to polystyrene 100:10. Under these conditions, the combustible recovery by carrier flotation was obtained as 70.59% when the ash content was 12.32%, which increased by 25.68 points compared with the combustible recovery of conventional flotation under almost the same ash content. The fine coal particles coated the coarse polystyrene particles through hydrophobic interactions between the polystyrene and hydrocarbon chains of the kerosene adsorbed on coal particles. The results suggested that the flotation performance of low-rank coal was significantly improved by carrier flotation with polystyrene, especially for fine particles.

Coal fly ash (CFA), hazardous to the environment and human health, has been considered to be a potential alternative source for rare earth elements (REEs) in recent years. However, information on how REEs distribute and occur in coal fly ash is still incomplete. In this work, particle size analysis, inductively coupled plasma–mass spectrometry, scanning electron microscopy, and electron probe microanalysis were applied to study the occurrence and distribution of REEs in a fly ash sample from the Qianxi coal-fired power plant in Guizhou province. The results show that the REEs content in the CFA was 630.51 ppm. Wet grinding-enhanced leaching experiments revealed that a part of the rare earth particles was encapsulated within the glass body. These rare earth particles could be liberated and released to a certain extent by wet grinding, which would increase the acid-leaching recovery of REEs from 23.49% to 41.68%. This study classifies the speciation of REEs in coal fly ash as (1) amorphous glassy particles with REE minerals or compounds encapsulated inside; (2) amorphous glassy particles with REEs distributed throughout; and (3) discrete REE minerals or compounds. The results of this study are a basis for developing an economically viable and environmentally sustainable technology for recovering REEs from CFA.

One antibacterial material was prepared from exfoliated graphite (EG) decorated with silver nanoparticles (AgNPs). The EG was prepared by the graphite intercalated compound process, AgNPs were prepared by chemical reduction of AgNO₃ in the presence of NaBH₄. The AgNPs-loaded EG (Ag-EG) composite was characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), nitrogen adsorption, mercury intrusion porosimetry, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The antibacterial effect of the Ag-EG was evaluated by using the zone of inhibition method. The loaded AgNPs were highly dispersed on EG sheets and most of them have a size less than 10 nm. The Ag loading slightly increased the surface area of EG. It is shown that the Ag-EG had antibacterial activity and anti-adhesion properties against Pseudomonas aeruginosa and Staphylococcus aureus. It suggests that Ag-EG composites could be used in a variety of industrial applications that require an antibacterial effect.

The preparation of substrate with high specific surface area and conductivity is very important in the development of non-enzymatic glucose sensors. This study presents a non-enzymatic glucose sensor electrode based on a hybrid reduced graphene oxide (rGO) and carbonized silk fabric (CSF) substrate obtained by immersing silk fabric in a graphene oxide solution and carbonizing at 950 °C in an Ar atmosphere, and then decorating the rGO/CSF surface with Cu nanoflowers by electrodeposition. The optimum Cu-rGO/CSF sensor electrode exhibits high glucose sensitivities of 6613.3 μA mM⁻¹ cm⁻² and 1541.7 μA mM⁻¹ cm⁻² with linear responses over separate glucose concentration ranges of 0.05–4.0 mM and 4.0–7.0 mM due to the rGO/CSF substrate has high specific surface area, good conductivity and the Cu nanoflowers have high catalytic activity. The electrode also provides a lower limit of detection of 2.27 μM at a signal-to-noise ratio of 3 and high stability in the air. These results demonstrate that the proposed electrode material facilitates the development of simple and accurate non-enzymatic glucose sensors.