粉末挤出打印制备异型UO2-W燃料的脱脂-烧结工艺优化与致密化研究

Optimization of Debinding-Sintering Processes and Densification Study on Fabricating Complex-shaped UO2-W Fuel via Powder Extrusion Printing

  • 摘要: 钨基二氧化铀(UO2-W)金属陶瓷燃料因其高熔点、优异导热性及辐照稳定性,在空间核热推进系统中具有重要应用潜力。钨金属熔点高、硬度大,传统粉末冶金工艺难以实现异型钨基金属陶瓷燃料结构的精密成型,而粉末挤出打印(PEP)技术可通过逐层堆积实现钨基燃料的高精度成型。针对核热推进系统对异型UO2-W金属陶瓷燃料的研发需求,通过优化蜡基黏结剂配方,制备出UO2体积分数≥55%的均匀喂料;采用PEP技术实现蜂窝状UO2-W燃料芯块的成型;结合正庚烷脱脂与氢气烧结,成功制备出UO2-W燃料芯块样品。性能检测结果表明,芯块样品中UO2与W分布均匀,密度达理论密度的96%以上,硬度达520 HV。本研究验证了PEP技术在异型金属陶瓷燃料制备中的可行性,为复杂形状燃料的设计制造提供了工艺基础。

     

    Abstract: To meet the demands of future complex space missions, more advanced space propulsion systems are essential. Among these, nuclear thermal propulsion (NTP) systems offer high specific impulse, high thrust, and long operating times, making them an ideal choice for propulsion needs in manned deep space exploration, large interplanetary transportation, and space weapons platform maneuvering. The NTP system design often employs complex structures of tungsten-based uranium dioxide (UO2-W) CERMET fuel elements, typically configured as honeycomb structures with multiple elongated coolant channels uniformly distributed throughout the fuel pellets. The intricate design of CERMET fuels, combined with the high melting point and hardness of tungsten, poses significant challenges for the molding and production of these fuel elements. Powder extrusion printing (PEP) technology, an emerging additive manufacturing technique, can achieve near-net-shaping of complex structures while reducing heat treatment temperatures, thereby significantly simplifying the fabrication process of cermet fuel elements. To address the developmental needs for complex-shaped UO2-W CERMET fuels in NTP systems, PEP technology was utilized and the debinding and sintering processes were systematically optimized, enabling efficient fabrication and densification of complex-shaped fuels. By optimizing a wax-based binder formulation, a uniform feedstock with a UO2 volume fraction of ≥55% was developed, effectively mitigating the segregation issues caused by the large density differences between UO2 and W. The feedstock was processed using PEP technology, followed by n-heptane debinding (50 ℃, 12-72 h) and hydrogen sintering (1 900 ℃, 6 h holding time). Dense honeycomb-shaped fuel pellet samples were successfully fabricated, achieving a density of about 97% of the theoretical density. Microstructural characterization revealed uniform distribution of UO2 and W without significant phase separation, with post-sintering W grain sizes of 5-8 μm and a hardness of about 520 HV. During the debinding process, n-heptane achieved a debinding rate of over 85%, while forming interconnected pore channels that provided ideal diffusion pathways for subsequent sintering. In the sintering stage, the hydrogen atmosphere effectively suppressed the formation of tungsten surface oxides, promoting grain boundary migration and pore closure. Optimization of the sintering process indicated that sintering at 1 900 ℃ resulted in an open porosity of <2.5%, although the grain size was relatively large. Furthermore, the corrosion resistance of the fabricated materials was indirectly inferred from their dense microstructure and low porosity, which minimize surface area exposed to corrosive environments. The hydrogen sintering atmosphere further enhances resistance by reducing oxide formation on tungsten surfaces. The low-porosity, uniform, and low-oxide-content surface state is crucial for improving the long-term corrosion resistance and service reliability of fuel elements in the high-temperature hydrogen coolant environment of NTP systems. This study validates the feasibility of PEP technology for the fabrication of complex-shaped nuclear fuels, overcoming the limitations of traditional processes in terms of complex shape formation and densification. Through the synergistic optimization of debinding and sintering processes, the densification of complex-shaped UO2-W fuels was achieved, providing critical technical support for the development of NTP systems.

     

/

返回文章
返回