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ORNL-TM-7207 - the Molten Salt Energy Technologies Web Site

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3.3.1.1 Composition of DMSR fuel<br />

47<br />

3.3-1 Basic considerations<br />

Choice of initial composition. A DMSR will derive some of its fis-<br />

sion energy from plutonium isotopes, but 2 3 3 ~ and '3% will be <strong>the</strong> primary<br />

fissile isotopes, while '32~h, with important assistance from 2 48~, is <strong>the</strong><br />

fertile material a<br />

concentration will need to be markedly higher than <strong>the</strong> total concentration<br />

of uranium isotopes.<br />

Clearly (see previous neutronics discussion) <strong>the</strong> 232~h<br />

The only stable fluoride of thorium is ThF4; thus, it must be used in<br />

such fuels. Puke UF3 is appreciably disproportionated at high tempera-<br />

tures by <strong>the</strong> reaction<br />

Generally in molten fluoride s~lutions, this reaction proceeds appreciably<br />

at lower temperatures.<br />

fuel by reaction (reduction) of UP4 with species within <strong>the</strong> container<br />

metal and, as explained below, a small quantity of UF3 deliberately main-<br />

tained in <strong>the</strong> fuel serves as a very useful reduction-oxidation (redox)<br />

buffer in <strong>the</strong> fuel. Such UF3 is sufficiently stable in <strong>the</strong> presence sf<br />

a large excess of UP,, but UF4 must be <strong>the</strong> major uranium species in <strong>the</strong><br />

fuel. 19320<br />

also by LE,), and PuF3 is <strong>the</strong> stable fluoride of this element in DMSR<br />

fuels.<br />

A small amount of UF3 will be formed within <strong>the</strong><br />

~onversely, PUF~ is reduced by <strong>the</strong> metallic container (and<br />

Phase equilibria among <strong>the</strong> pertinent fluorides have been defined in<br />

detail and are well documented. 19-21 Because <strong>the</strong> concentration of ThF4<br />

is much higher than that of UF4, <strong>the</strong> phase behavior of <strong>the</strong> fuel is dic-<br />

tated by that of <strong>the</strong> LiP-BeF2-ThF4 system shown in Pig. 11.<br />

3LIP*ThF4 can incorporate Be2* ions in both interstitial and substitu-<br />

tional sites t o form solid solutions whose compositional extremes are rep-<br />

resented by <strong>the</strong> shaded triangular region near that compound. The maximum<br />

ThF4 concentration available with <strong>the</strong> liquidus temperature below 500°C is<br />

just above 14 mole %. Replacement of a moderate amount of ThP4 by UF4<br />

scarcely changes <strong>the</strong> phase behavior.<br />

The compound

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