It is imperative to have an in-depth understanding of the effect of extraneous moisture on the spontaneous combustion of coal not only for the control and prevention of coal spontaneous combustion in the coal mining industry, but also for the optimization design and application of the technological process. In this study, the type of moisture in a coal body has been redefined for the first time from the perspective of disaster prevention and control, i.e., original occurrence of moisture in the coal matrix and the extraneous moisture from the technological process. A suit of coal bodies with different extraneous moisture was prepared by soaking long-flame coal with a low water content. Using a temperature-programmed oxidation test, the effects of extraneous moisture on the temperature increase rate of coal bodies and the emission characteristics of gaseous products during coal spontaneous combustion were studied. Moreover, combined with the characterization of thermal analysis and of pore structure test, the action the mechanism of extraneous moisture on the coal spontaneous combustion process was also explored. The experimental results indicated that the effect of the extraneous moisture content varied with the development of coal spontaneous combustion. In the slow oxidation stage, extraneous moisture played a physical inhibition role in the coal oxidation. In the accelerated oxidation stage, extraneous moisture exhibited a catalytic effect on the coal–oxygen reaction or directly participated in the reaction. After entering the rapid oxidation stage, a delayed effect appeared. When the coal temperature exceeded 180 °C, the spontaneous combustion characteristics of coals with different initial moisture contents gradually tended to achieved balance.

Temperature changes in CO₂ foam-fracturing construction can easily affect surfactant foam stability. To investigate the effect of temperature on the foam stability of different types of surfactants, this study measured the foam half-life and viscosity of four typical surfactants, CTAB, LAS-30, HSB1214, and TX-10, using a novel self-designed and built foam performance measurement device. The effects of temperature on foam half-life and viscosity were studied. The results show that as the temperature increased, the half-life shortened, and the viscosity of the liquid phase decreased, which led to a decrease in foam stability. Moreover, using Materials Studio, a type of molecular simulation software, an interfacial model of the foam film was constructed to calculate the IFE and the self-diffusion coefficient of water molecules at 300 ps after the equilibrium of the foam system to investigate the mechanism of temperature influence on the stability of the foam. The results show that, for CTAB, LAS-30, HSB1214, and TX-10, the temperature increases from 15 °C to 45 °C, the IFE is enhanced by −50.05%, −59.10%, −64.21%, and −44.26%, respectively, the interfacial system changes from a low-energy state to a high-energy state, and the interfacial stability decreases. Meanwhile, D_water increased 1.10-fold, 0.78-fold, 1.43-fold, and 0.64-fold, respectively, which accelerated the diffusion and migration of water molecules, weakened the intermolecular forces, and accelerated the instability of the foam system.

Long-term accumulation of coal gangue hill has a high risk of spontaneous combustion, and the toxic and harmful gases emitted by spontaneous combustion seriously pollute the atmosphere. The key to managing the spontaneous combustion fire of coal gangue hill lies in the accurate measurement of fire source location. However, measuring the fire source location of surface coal gangue hill lacks experimental and empirical research. In this paper, an oxidation warming experiment was conducted on the coal gangue samples, and the law of radon gas exhalation from coal gangue under different temperatures was analyzed. At the same time, surface thermometry and isotope radon measurement were applied to measure the high-temperature areas inside the gangue hill, and the measurement results were compared. The experimental results show that as the temperature of gangue increases, the amount of radon gas exhalation in gangue shows a changing trend of rising first and then decreasing. The radon exhalation from coal gangue can be divided into three stages. In the I stage (30 ~ 100°C), the evaporation of pore water in coal gangue leads to the exhalation of radon in water, causing the increase of radon concentration; in the II stage (100 ~ 350°C), the coal gangue is pyrolyzed at high temperature, and a large amount of radon is exhalated from the closed pores; in the III stage (350 ~ 450°C), after the first two stages of radon release, the number of radon atoms in this stage decreases, leading to a rapid decrease of radon concentration. The field measurement results show that compared with the surface thermometry method, the isotope radon measurement method is less disturbed by external conditions, and the circled fire area is more accurate, which has essential theoretical significance and practical application value for the accurate measurement of fire source location in coal gangue hill.

The threshold dilution ratio of acetaldehyde is much larger than those of other odor compounds generated during the spontaneous combustion process and so it is the most important odorant. Studying the mechanism by which acetaldehyde is generated can provide the necessary theoretical support for acetaldehyde-based odor analysis. In the present work, the release of acetaldehyde was monitored while heating lignite, long-flame coal, and coking coal specimens under either air or nitrogen. The data show that acetaldehyde was primarily produced by the oxidation of active sites in the coal rather than by the pyrolysis of oxygen-containing functional groups. Based on quantum chemistry and coal-oxygen reaction theory, the transition state approach was used to further study the formation of acetaldehyde during the low-temperature oxidation of coal. Using density functional theory, three different coal molecule structures were modeled and optimized structures for acetaldehyde formation and the energies, bond lengths, and virtual frequencies of each reaction stagnation point were obtained at the B3LYP-D3/6-311G** and M062X-D3/Def2-TZVP levels. The results indicate that the low-temperature oxidation of coal to generate acetaldehyde involves the capture of H atoms from aliphatic side chains to generate peroxy radicals. These radicals then attack unsaturated C atoms through complex inversions to generate peroxides. In the third step of this process, the O-O single bonds in the peroxides break in response to thermal energy to form carbonyl groups. Finally, specific C-C or C-O bonds on the aliphatic side chains are thermally cleaved to generate acetaldehyde.