Abstract
The difficulties encountered in conventional sintering of uranium monocarbide impose serious economic restrictions on the use of this potentially important nuclear fuel. At the high temperatures ordinarily used for sintering, chemical control of the carbide is ineffective and the resultant density is not attractively high. Sintering aids alleviate these difficulties, but any microconstituents resulting from the additive should be eliminated to avoid adverse effects in service.
Three processes have been developed using different sintering aids to consolidate high-purity uranium monocarbide powders below 1600°C to compacts having densities ranging from 95 to greater than 97% of theoretical. Our additives were 7.5% UAl2, 0.75% UBe13, and 0.75% U3Si2; during sintering they were eliminated by either evaporation or dissolution into the carbide. The U3Si2 process holds the greatest promise, since it showed near insensitivity to variations in charge-carbon content and proved highly effective even for UO2-derived carbide powder that has a high oxygen content.
To aid interpretation of the sintering mechanisms, we determined pertinent pseudobinary phase diagrams and derived tentative ternary isotherms at the sintering temperatures. An important feature of these processes was an initial stage in which reactive metal vapor issued from the additive and promoted substantial shrinkage. When highest densities were obtained, this stage was generally followed by liquid-phase sintering. Single-phase compacts were ultimately achieved by either dissolution within the matrix or carburization of the residual constituent.
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© 1966 Metal Powder Industries Federation and The Metallurgical Society of AIME
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Hammond, J.P., Adamson, G.M. (1966). Activated Sintering of Uranium Monocarbide. In: Hausner, H.H. (eds) Modern Developments in Powder Metallurgy. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-7712-2_1
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DOI: https://doi.org/10.1007/978-1-4684-7712-2_1
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