Xiaojun Zhao

To address the escalating demand for ultra-high-purity tungsten in advanced applications such as semiconductor targets and nuclear-grade shielding, this study synergistically coupled the processes of thermal decomposition, ammonia dissolution, and segmented evaporation crystallization. The optimal parameters for the thermal decomposition and ammonia dissolution stages were subsequently identified through systematic optimization. By independently regulating the nucleation and crystal growth processes during the crystallization of ammonium paratungstate (APT), the limitation of traditional methods, which require multiple crystallization cycles to achieve high purity, is effectively overcome. Experimental results demonstrated that under optimized conditions—thermal decomposition at ~280 °C and ammonia dissolution at 90 °C—high-purity APT (4N5 grade, total impurities < 50 ppm) was achieved in a single crystallization cycle. Furthermore, under segmented crystallization conditions (nucleation at 80 °C with a stirring speed of 1.26 m/s and growth at 90 °C with a stirring speed of 1.09 m/s), the product exhibited an average particle size of 34.43 μm and a direct recovery efficiency of 73.1%. By suppressing burst nucleation and reducing impurity adsorption, this process provides a critical technological pathway for large-scale production of ultra-high-purity tungsten materials.

To address the surface wear issues of tungsten alloys in die-casting mold applications—where low hardness coupled with severe service conditions involving high-pressure impact from molten metal, thermal cycling, and component counter-friction—this study employed three techniques: laser cladding, plasma spraying, and vacuum surface carburization. Three distinct strengthening coatings were prepared on a tungsten heavy alloy (WHA) substrate. X-ray diffraction (XRD), scanning electron microscopy (SEM), a Vickers hardness tester, and block-on-ring friction and wear tests were employed to characterize the phase composition, microstructure, hardness, and wear resistance of the coatings. The results indicate that all three coatings significantly enhanced the hardness of the substrate, albeit through different strengthening mechanisms. The hardness increase in the laser-clad coating is attributed to the combined strengthening effect of rapid solidification-induced fine grains and dispersed WC particles. The enhanced hardness of the plasma-sprayed coating is due to the intrinsic hardness of WC and its dense layered structure. The carburized layer exhibits the highest hardness, resulting from the continuous WC phase formed via in situ reaction and an interface-free gradient transition with the substrate, which eliminates interfacial weak zones. Under loads of 50 N and 100 N, the plasma-sprayed coating demonstrated the best wear resistance, with wear volumes of 0.16% and 0.18% of that of the substrate, and wear depths of 4.57% and 3.50% of that of the substrate, respectively. It also exhibited the optimal load adaptability, making it a preferred solution for surface strengthening of tungsten alloy die-casting molds.

GH3039 nickel-based alloy, as a key material for thermocouple protection tubes, is susceptible to wear and oxidation failure in high-temperature kiln environment. To address this, boronized, chromized and borochromized coatings were prepared on GH3039 substrate, and the friction-wear properties and high-temperature oxidation resistance of both the substrate and the coatings were systematically characterized. The results show that the borochromized coating, benefiting from the synergistic effect of its relatively high surface hardness and the boric acid lubricating film formed during the wear process, reduces the wear rate by 84.07% (to 1.44 × 10⁻⁵ mm³·N⁻¹·m⁻¹). Meanwhile, it exhibits the optimal oxidation resistance due to its dense Cr-rich layer, which can inhibit oxygen diffusion and supply chromium for protective Cr₂O₃ film. After 100 h of oxidation at 950 °C, its oxidation weight gain is reduced by 78.68% compared with the boronized sample (to 1.20 mg/cm²).

The insufficient corrosion resistance and high interfacial contact resistance (ICR) of 316L stainless steel (316L SS) severely limit its application as bipolar plates (BPs) in proton exchange membrane fuel cells (PEMFCs). In this study, a graphite/carbon black/PVDF composite coating was first developed by hot rolling on the surface of 316L SS to enhance both corrosion resistance and conductivity. By incorporating 5 wt% polyaniline (PANI) as a corrosion inhibitor, the optimized RP5 coating exhibited further improvements in corrosion resistance. The potentiodynamic polarization tests revealed that the RP5 coating achieved a corrosion current density of 0.977 μA·cm⁻², representing a two-orders of magnitude reduction compared to bare 316L SS (34.1 μA·cm⁻²). The coating also exhibits a satisfactory interfacial contact resistance (ICR) of 8.20 mΩ·cm² at 1.5 MPa, meeting the U.S. Department of Energy (DOE) 2025 targets (2). Additionally, the RP5 coating exhibited superior hydrophobicity with a water contact angle of 96.5°, which is advantageous for water management within PEMFCs. The results confirm that the RP5 coating achieves an optimal balance between high conductivity, excellent corrosion resistance, and improved hydrophobicity, making it a promising solution for advancing PEMFC bipolar plates’ performance.

High-reflectivity metallic films on aluminum substrates are crucial in advanced aerospace and military applications due to their excellent reflectivity and workability. In order to further improve the reflectivity and thermal stability of films, this study investigated the deposition of AgInCu_x (x = 1, 3, and 5 wt.%) films on Al 6061 alloy substrates using magnetron sputtering, exploring the impact of deposition parameters and composition on their optical properties and thermal stability. Increased copper content improved thermal stability, while it compromised reflectivity. Additionally, increasing deposition power and time initially enhanced reflectivity, but beyond an optimal point, it decreased. Therefore, the AgInCu films deposited at 30 W for 2 min exhibited the highest reflectivity of 99.8% in the near-infrared range, making them promising candidates for reflective films in next-generation optical applications.

Advancements in electrical components have intensified the challenges for copper alloy wear resistance and high-temperature performance in electrical applications. The surface coating preparation of Cu alloys is crucial for enhancing their lifespan and promoting sustainable resource development. This study explored the microstructure and properties of Cu-Cr-X coatings (X = Mo/W, Al₂O₃/TiO₂) on Cu alloy substrates via laser-cladding to improve wear resistance and hardness, vital for electrical component reliability and switching capacity. The process involved adjusting the power and reinforcing the phase particle size. The results showed hardness > 110 HV for all coatings (vs. 67.4 HV for the substrate). Cu-Cr-W achieved the highest hardness at 179 HV due to W dispersion and WCr precipitate reinforcement. It also maintained a stable CoF and the lowest wear rate (1.87 mg/km), with a fivefold wear resistance compared to the substrate alone. Cu-Cr-W excelled in lifespan extension and material loss reduction due to superior hardness, wear resistance, and conductivity.

A novel TiB₂-CeO₂-modified (Nb,Mo,Cr,W)Si₂ coating was prepared on a Nb-5W-2Mo-1Zr alloy substrate using two-step slurry sintering and halide-activated pack cementation to address the limitations of a single NbSi₂ coating in meeting the service requirements of niobium alloys at elevated temperatures. At 1700 °C, the static oxidation life of the coating exceeded 20 h, thus indicating excellent high-temperature oxidation resistance. This was due to the formation of a TiO₂-SiO₂-Cr₂O₃ composite oxide film on the coating surface, which, due to low oxygen permeability, effectively prevented the inward infiltration of oxygen. Additionally, the dense structure of the composite coating further enhanced this protective effect. The composite coating was able to withstand over 1600 thermal shock cycles from room temperature to 1700 °C, and its excellent thermal shock performance could be attributed to the formation of MoSi₂, CrSi₂, and WSi₂ from elements such as Mo, Cr, and W, which were added during modification. In addition to adjusting the difference in thermal expansion coefficients between the layers of composite coatings to reduce the thermal stress generated by thermal shock cycles, the formation of silicide compounds also improved the overall fracture toughness of the coating and thereby improved its thermal shock resistance.