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for 5 min at 3000 psi at 1150, 1200,<br />

and 1250OC in an argon atmosphere.<br />

Fur<strong>the</strong>r tests have been run at 1150°C<br />

for 1, 10, and 30 min to determine<br />

<strong>the</strong> effect of time on <strong>the</strong> extent of<br />

bonding. Evaluation of <strong>the</strong>se tests<br />

is not complete.<br />

Examination of <strong>the</strong> first group of<br />

samples revealed little difference in<br />

<strong>the</strong> degree of bonding at <strong>the</strong> various<br />

temperatures. As was expected, considerably<br />

more diffusion occurred at<br />

1250'C than at <strong>the</strong> lower temperatures,<br />

but bonding was only slightly better.<br />

In general, <strong>the</strong> various couples may<br />

be divided into four groups on <strong>the</strong><br />

basis of <strong>the</strong> extent of bonding: excellent,<br />

interface almost obliterated,<br />

insep ar ab1 e; good, inter face we1 1<br />

de fined, in sep ar ab1 e; fa i r , sep ar a te d<br />

with some di f f i cul ty; poor, only<br />

* superficial bonding. The couples<br />

studied fall into <strong>the</strong>se categories in<br />

<strong>the</strong> following manner:<br />

Exce 1 Zen t<br />

Nickel to Inconel<br />

Nickel to stainless steel<br />

Stainless steel to stainless steel<br />

Iron to iron<br />

Good<br />

Nickel to iron<br />

Nickel to nickel<br />

Molybdenum to nickel foil to molybdenum<br />

Farr<br />

Molybdenum to nickel<br />

Molybdenum to Inconel<br />

Molybdenum to molybdenum<br />

Poor<br />

Molybdenum to iron<br />

Molybdenum to stainless steel<br />

The self-welding of <strong>the</strong> molybdenum,<br />

with or without a nickel foil bonding<br />

layer, was poor at 1ZSO'C; so supplementary<br />

runs were made at 1400 and<br />

1500°C, with results as indicated<br />

above.<br />

For molybdenum to nickel and molybdenum<br />

to Inconel, <strong>the</strong>re was a<br />

measurable amount of diffusion but<br />

only fair bonding, possibly because<br />

of <strong>the</strong> formation of a third phase of<br />

PERIOD ENDING DECEMBER 10, 1952<br />

poor strength at <strong>the</strong> interface. EX-<br />

tensive diffusion (2 to 3 m i l s )<br />

occurred between molybdenum and iron<br />

and molybdenum and stainless steel,<br />

but <strong>the</strong>re was even less bonding than<br />

was found between molybdenum and<br />

nickel or between molybdenum and<br />

Inconel.<br />

Fur<strong>the</strong>r work in which electro-<br />

deposited chromium is used as a bonding<br />

layer is being done on <strong>the</strong> bonding of<br />

molybdenum to <strong>the</strong> o<strong>the</strong>r metals.<br />

Chromium is reported to be completely<br />

miscible with molybdenum and may be<br />

more compatible with <strong>the</strong> o<strong>the</strong>r ma-<br />

terial s.<br />

Several small fuel assemblies have<br />

been prepared by using <strong>the</strong> electro-<br />

formed nickel screen, filling with<br />

mixtures of UO, and stainless steel<br />

powder, and pressing rubberstatically.<br />

This step is followed by cladding both<br />

sides with iron or nickel sheet and<br />

by hot pressing at 1250°C. The as-<br />

semblies are now being examined for<br />

fuel distribution and bond integrity.<br />

COLUMBIUM RESEARCIl<br />

E. S. Romar H. Inouye<br />

Me tal lurgy Division<br />

Gaseou s Reac t ions. I nve s ti ga ti on<br />

of <strong>the</strong> reaction of gases with colurnbi-<br />

um was initiated after a literature<br />

survey was made that revealed <strong>the</strong><br />

high reactivity oi <strong>the</strong> metal above<br />

400°C and some preliminary high tem-<br />

perature tests made that gave erratic<br />

results. Minute quantities of dis-<br />

solved gases change <strong>the</strong> mechanical<br />

properties considerably, and hence<br />

<strong>the</strong>se reactions must be controlled.<br />

The primary interest during this<br />

period was in finding a suitable<br />

atmosphere in which to conduct creep<br />

tests. An argon atmosphere was<br />

selected, initially, and some of <strong>the</strong><br />

observations are presented in Table<br />

12.1. Commercial, tank argon was<br />

purified by drying with a tower of<br />

m agne si um perchlorate , fo 1 lowed by<br />

157

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