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METALLOTHERMIC REDUCTION OF YTTRIUM HALIDES

Technical Report ·
OSTI ID:4694115

An investigation was made of methods to prepare highpurity yttrium metal. Various methods were used to prepare pure intermediate compounds, primarily cblorides, bromides, and iodides, which were subsequently reduced to metal. The process found most suitable for the preparation of pure anhydrous yttrium chloride involved thermal dehydration of a mixture of hydrated yttrium chloride and ammonium chloride while under vacuum. Yttrium bromide and iodide were prepared most effectively by the direct halogenation of yttrium carbide. Yttrium carbide was obtained by reacting and melting yttrium oxide-- carbon mixtures in a carbon-arc furnace. Yttrium halides were purified by vacuum distillation and reduced by alkali or alkaline-earth metals. Lithium and sodium proved to be the best reductants from the standpoint of yield ()96%) and purity ()99.8%) of the yttrium. The product of the reduction step was sponge metal, which was consolidated readily by conventional cold-mold, arc-melting procedure. The purest yttrium obtained in laboratory scale work was prepared by sodium reduction of yttrium cbloride and contained only 125 ppm oxygen; other imparities did not exceed 1,660 ppm. In larger scale tests ytirium containing ouly 800 to 1,000 ppm total impurities was obtained by lithium reduction of yttrium chloride. The tensile properties of high-purity yttrium were determined. Mechanical tests showed that yttrium can be forged, extuded, rolled, spot welded, and deep drawn. (auth)

Research Organization:
Bureau of Mines. Albany Metallurgy Research Center, Ore.
NSA Number:
NSA-17-029247
OSTI ID:
4694115
Report Number(s):
BM-RI-6259
Country of Publication:
United States
Language:
English