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To study the effect of erosion on coal microstructure and its oxidation characteristics, eroded coals were prepared by eroding coal samples in an acidic aqueous solution for 30 days, 90 days and 180 days, respectively. The microcrystalline structure, pore structure and active groups distribution of coal samples were studied using X-ray diffractometer, low-temperature N 2 adsorption and infrared spectra. Temperature-programmed experiment was used to analyze the oxidation characteristics of raw coal and eroded coals. The results reflected that the number of aromatic layers and coalification degree of eroded coal are reduced compared with raw coal. The average pore diameter increases, which promotes oxygen transportation in coal pores. Under the erosion effects, the content of active groups such as hydroxyl (–OH), methylene (–CH 2), and methyl (–CH 3) in coal increases. Eroded coals, especially the coal eroded for 180-day demonstrate more oxygen consumption and CO production than raw coal during the oxidation process, and their apparent activation energies decrease. Besides, the enhancement mechanism of eroded coal's oxidation activity is expounded from the aspects of the increase of active sites and the improvement of pore structure. In brief, erosion effect increases the spontaneous combustion tendency of coal. • The effect of weak acid erosion with different durations on coal oxidation behavior was studied. • Changes of coal physicochemical structure after erosion effect were studied. • The apparent activation energy of eroded coal decreases during low-temperature oxidation. • Mechanism for easier oxidation of dried eroded coal was expounded. [ABSTRACT FROM AUTHOR]

In this work, cold drawing deformation was applied aiming to achieve a good combination of strength and electrical conductivity of Cu–20Fe alloy, and also such underlying mechanisms for microstructure evolution and strengthening, as well as variation in conductivity were clarified. It is also found that both Cu matrix grains and Fe-rich dendrites can be significantly refined and transformed into fibrous structure with increasing of drawing strain. The average size of Cu grains and thickness of Fe fiber are 0.47 ± 0.05 μm and 25 ± 5 nm, respectively for alloy subjected to the drawing strain of η = 5.78. In addition, the Fe dendrites exhibit a strong <110> fiber texture, while the corresponding Cu matrix forms a <111> fiber texture. It is demonstrated that the excellent properties with the yield strength of 1173 MPa and the electrical conductivity of 41 %IACS can be reached for cold-drawn Cu–20Fe alloy. In addition, the quantitative analysis on strengthening contributions shows that the high strength of as-drawn Cu–20Fe alloy is dominantly originated from high-density Fe fibers. Meanwhile, the lower electrical conductivity is ascribed to the high solute Fe content and high-density Cu/Fe heterogeneous phase interface. • The microstructure evolution and properties of Cu–20Fe alloys at different drawing strains were clearly elucidated. • The Cu–Fe dual-phase co-deformation behavior during drawing deformation process was described. • A strengthening model of Cu–Fe dual phase alloy under severe plastic deformation was established. • The Cu–20Fe alloy achieves a good combination of mechanical and electrical properties at drawing strain of η = 5.78. [ABSTRACT FROM AUTHOR]

A refractory high entropy alloy (RHEA) NbHfTiV was selected as the master alloy and carbon element was introduced to synthesize the novel NbHfTiVC x RHEAs (x = 0, 0.1, 0.2, 0.3), which perform outstanding strength and excellent ductility simultaneously. Phase identification, microstructure evolution, and mechanical properties were systematically analyzed. The results show that the primary MC-type carbides and nano-precipitate carbides are generated in the BCC matrix phase with the addition of carbon. The primary carbides evolve from solid spheroid (x = 0.1) to sandwich-like pattern (x = 0.2, 0.3), and grain size is significantly refined from 537 µm (x = 0) to 25 µm (x = 0.3). Compressive tests show that the yield strength increases from 958 MPa to 1115 MPa, and the fracture mechanism is changed from ductile fracture to ductile and brittle mixed fracture with carbon content increasing. Meanwhile, the atomic size mismatch and elastic mismatch of the matrix phase reduce with carbon content increasing, which could decrease the lattice distortion degree and soften the matrix phase. [Display omitted] • Carbides (FCC-MC) are generated in BCC matrix with the addition of carbon. • After adding carbon, the grain size is greatly refined from 537 to 25 µm. • Increasing carbon content release severe lattice-distorted and soften the matrix. • Yield strength of NbHfTiVC x RHEAs increase from 958 (C 0) to 1115 MPa (C 0.3). [ABSTRACT FROM AUTHOR]

In the present study, the effect of C micro-alloying on microstructure evolution and properties of metastable immiscible Cu-20Fe alloy was comprehensively investigated. Experimental results indicate that the microstructure of Cu-Fe alloy is extremely sensitive to the C content. It was found that obvious liquid-liquid phase separation (LLPS) behavior is observed in Cu-20Fe alloy after C micro-alloying, and the tendency of LLPS is enhanced with increasing C content. The calculation of ΔScc(0) suggests that C atoms preferentially pair with free Fe atoms to form new Fe (C) atomic clusters, thus resulting in the enhancement of bonding of the like-atom pairs. In addition, the quasi-binary phase diagram calculation further reveals the existence of a stable miscibility gap for C-containing alloys, and the temperature interval of miscibility gap is significantly enlarged with increasing C content. Meanwhile, the interface energy between two liquids formed by LLPS also slightly increases as C content increasing. These above reasons should be responsible for the microstructure evolution of Cu-20Fe-xC alloys. In addition, the C micro-alloying deteriorates the soft magnetic properties of Cu-Fe alloys to a certain extent, whereas improves its corresponding wear-resistance. • The microstructure evolution and solidification behavior of Cu-20Fe-xC alloys were clearly elucidated. • The calculation of ΔScc(0) indicates that C atoms preferentially pair with free Fe atoms to form new Fe(C) atomic cluster. • Phase calculation indicates that the metastable miscibility gap of Cu-20Fe alloy is stabilized by the introduction of C. • The addition of appropriate amount C enhances the wear-resistance of Cu-20Fe alloy. [ABSTRACT FROM AUTHOR]