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ORNL-1771 - Oak Ridge National Laboratory

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4NP QUARTERLY PROGRESS REPORT<br />

on d<br />

3FeC12 = 2FeCI, + Fe , Fo = 0.35 V.<br />

The NiCI, solutions, as far as is known, undergo<br />

the same electrochemical reactions regardless of<br />

concentration. Thus the changes in decomposition<br />

potential with concentration may be assigned to<br />

differences in NiC!, activity alone. With the aid<br />

of the Nernst equation, the NiCI, activity at 33.3<br />

mole % NiCI, may be coniputed to be 100 times that<br />

in the 3.3 mole 76 solution and 300 times that in<br />

the 1 mole % solution.<br />

Solubility of Xenon in Molten Salts<br />

R. F. Newton, Researcli Director's Department<br />

D, G. Hill, Consultant<br />

The use of molten salts as reactor fuels offers<br />

the possibility of removing the gaseous fission-<br />

product poisons, of which zmon is the rnost im-<br />

portant, If, for example, the xenon concentration of<br />

the SO-Mw CFRE can be held at 10% of its equi-<br />

librium value (1.1 x mole of xenon per milli-<br />

I iter of fuel), important perturbations in reactivity<br />

can be avoided, In on aircraft reactor, however,<br />

it will be nccessary to effect this removal nd xenon<br />

with on absolute minimum of ouxiIiary equiprrient.<br />

The available literature appears to contain no<br />

measureinents of she solubility of gases in molten<br />

salts. Accordingly, it has seemed desirable to<br />

evaluate the solubility of xenon in molten fluorides<br />

over the temperature range of interest. Preliminary<br />

tests indicate that the following experimental tech-<br />

nique is satisfactory.<br />

The apparatus, which is constructed of nickc!<br />

where it will be in contact with the fluoridc melt<br />

and of glass elsewhere, consists of two sections<br />

that can be isolated by freezing a plt~g of fluoride<br />

in the U-tube connecting them, In one section of<br />

the apparatus the melt is allowed to saturate with<br />

xenon under predetermined conditions of ternpera-<br />

ture and pressure. Melting of the fluoride plug<br />

permits the saturated salt to flow into the other<br />

section, whi!e the 1J-tube seal prevents entrance of<br />

gaseous xenon into this section; refreezing of the<br />

plug isolates the sections again. 117 the second<br />

section, xenon is stripped from the salt by repeated<br />

circulation of the hydrogen contained in the a p p<br />

ratus through the salt and past a liquid-nitrogen-<br />

cooled trap. After the stripping process is com-<br />

plete, the hydrogen is removed, $he xenon is allowed<br />

to come to room temperature, arid he amount col-<br />

70<br />

lected is ascertained by measurements in a modi-<br />

fied Mcl_eod gage.<br />

Preliminary experiments at 600'6 and essentially<br />

1 atm of xenon indicate that the solubility in the<br />

NaF-KF-LiF eutectic is not greater than loM7<br />

mole of xenon per milliliter of salt. The method and<br />

technique proved to be feasible, but minor experimental<br />

difficulties necesFitatsd modification of<br />

the nickel apparatus. More accurate data under<br />

these and other conditions will be available in the<br />

near fWtIJre.<br />

Meanwhile, in order to gain familiarity with the<br />

technique, the solubility of xenon in the KNO,-<br />

NaNQ, eutectic (36 mole '36 NaNQ,) has been<br />

measured in an apparatus constructed entirely of<br />

glass. The solubility of xenon in this melt is<br />

about 8.5 x mole/itil at 280°C and low7<br />

mole/ml at 360°C. This liquid apparently shows<br />

the positive temperature coefficient of solubility<br />

expected for gases in molten salts.<br />

%-Ray DiFfr~~fi~n Studies in Salt Systems<br />

P. A. Agron M. A. Bredig<br />

Chemistry Division<br />

Cesium Halides. It has been suggested21t22 that<br />

the increase in volume on melting of simple binary<br />

salts is indicative ofstructural changes in the melt,<br />

that is, of a decrease to a lower ionic coordination.<br />

Volume increases up to 30% have been indicated for<br />

the alkali halides. The x-ruy data23 on the thermal<br />

expansion of solid CsBr and Csl gave volume<br />

changes of approximately 26%, but an extrapolation<br />

of about 50°C to their melting points WQS required<br />

for the computation of these changes. It WQS there-<br />

fore of interest to uscertain whether a solid-phase<br />

transition analogous to the one known to exist in<br />

CsCl occurs in the unexplored temperature interval.<br />

This would replace the assumed structural change<br />

in the melting process by one in the solid state.<br />

High-purity CsBr and Csl were intimately mixed<br />

with fine nickel powder to provide airs internal<br />

stairdurd whose thermal expansion is know BCCU-<br />

rate~y.,~ ~attice parameters as a function of tem-<br />

perature were obtained on the hi yh-temperature<br />

21J. W. Johnson, M. A. Bredig, and W. J. Smith, Gem.<br />

Dzv. @LOT. ?Tog. Rep. Der. 31, 1952, <strong>ORNL</strong>-1482, p 32.<br />

,P, A. Agron and M. A. Bredig, Ch~rn. Semzann. Prog.<br />

Rep. June 20, 1954, ORML-1755 (in press).<br />

24Ls Jo;dan and W. H. Swunger, J. Research Nnt. Bur.<br />

xtandn7ds 5, 123 i ( 1930)-

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