The evolution of pore structure during in situ underground exploitation of oil shale directly affects the diffusion and permeability of pyrolysis products. In this study, on the basis of mineral analysis and thermogravimetric results, in combination with the low-pressure nitrogen adsorption (LPNA) and mercury intrusion porosimetry (MIP) technique, the evolution of pore structure from 23 to 650 °C is quantitatively analyzed by simulating in situ pyrolysis under pressure and temperature conditions. Furthermore, based on the experimental results, we analyze the mechanism of pore structure evolution. The results show the following: (1) The organic matter of Fushun oil shale has a degradation stage in the temperature range of 350–540 °C, and there is no obvious temperature gradient between decomposition of kerogen and the secondary decomposition of bitumen. The thermal response mechanisms of organic matter and minerals are different in each temperature stage, and influence the change of pore structure. (2) Significant changes occur in pore shape at 350 °C, where thermal decomposition of kerogen begins. The ink-bottle pores are dominant when the temperature is less than 350 °C, whereas slit pores dominate when the temperature is greater than 350 °C. (3) The change in pore structure of oil shale is much less significant from 23 to 350 °C. The pore volume, porosity, and specific surface area (SSA) of samples increase rapidly with temperature varying from 350 to 600 °C. The variation of each parameter is dissimilated from 600 to 650 °C: the porosity and pore volume increases with a small gradient from 600 to 650 °C, and SSA decreases significantly. (4) The lithostatic pressure does not cause change in the evolution discipline of the pore structure, but the inhibitory effect on the pore development is significant.

Underground in situ pyrolysis and gasification is an important method to enable clean utilization of lignite in China. In this study, using the high-temperature triaxial permeability test equipment for different ranges of temperature and pore pressure, the permeability and mechanical characteristics of lignite from the Pingzhuang Mine Area in Chifeng have been examined. The results show that, at constant confining pressure, the elastic modulus of lignite decreases with increasing temperature. For temperature up to approximately 75°C, the elastic modulus is close to the modulus under the uniaxial state. As the temperature increases, the stress-strain curves during loading and unloading are different. The differences between the curves during loading and unloading are greater at higher temperature due to the greater residual deformation. In addition, in different temperature ranges (i.e., 150–650°C), the triaxial creep curves of lignite are different. In particular, at 300–450°C, the triaxial creep curve of lignite alternates between the accelerated creep and the steady creep. Moreover, the permeability change rule in the lignite is complex, and it is governed by the temperature and pore pressure. Hence, for different temperature range and pore pressure, the variations in the permeability are different. In fact, as the temperature increases, the permeability of lignite fluctuates.

In this research, corrugated Mg/Al clad sheet with good interface bonding was prepared with a rolling mill of upper corrugated roll and a lower flat roll under the conditions of 35% reduction and 400 °C. The mechanical properties of the corrugated Mg/Al clad sheet were studied using the transverse tensile test, Vickers microhardness and as well as its bending properties. Moreover, the interface bonding mechanism of the corrugated clad sheet was researched through three-dimensional contour analysis. The results showed that the UTS at the trough position was the highest (~296 MPa), and that the peak position was the lowest (~257 MPa). The maximum fracture EL at the peak position was ~13.4%, while the minimum fracture EL at the trough position was ~10.6%. In the transverse tensile process, the interface cracked first due to the uneven stress distribution in the matrixes. Then, the Mg sheet broke, and finally the Mg/Al clad sheet failed with final fracturing of the Al sheet. The microhardness of interface metal Al at the four positions was higher than that of the interface metal Mg, which was closely related to the dislocation strengthening of the Al sheet. The interface bonding mechanism of the corrugated Mg/Al clad sheet could be divided into four stages: extrusion deformation, rubbing fracture, compound extension and compound completion.