ORNL-4191 - the Molten Salt Energy Technologies Web Site
ORNL-4191 - the Molten Salt Energy Technologies Web Site
ORNL-4191 - the Molten Salt Energy Technologies Web Site
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f 243uUF,-7biF Fuel<br />
for <strong>the</strong><br />
J. M. Chandler<br />
Plans are nosv being made for refueling and op-<br />
erating <strong>the</strong> MSXE with 233U fuel early in 1968;<br />
approximately 40 kg of 233U as 233UF4-7LiF (27<br />
and 73 mole %) eutectic salt will be required.<br />
This material must be prepared in a shielded fa-<br />
cility because of <strong>the</strong> high 232U content (240 ppm)<br />
of <strong>the</strong> 233U. The following sections describe <strong>the</strong><br />
process, equipment, and status of <strong>the</strong> fuel prep-<br />
aration process.<br />
PROCESS<br />
'The process for preparing eutectic- UF4-T,iF (27<br />
and 73 mole %) salt for <strong>the</strong> original MSRE charge<br />
started with UF4 and LiF.' Since 233U is avail-<br />
able only as <strong>the</strong> oxide, <strong>the</strong> process was modified.<br />
The UO, is charged to a nickel-lined vessel, and<br />
LiF is added on top of it. 'The charge is heated,<br />
under helium, to 9QOOC to melt <strong>the</strong> LiF, which<br />
wets <strong>the</strong> oxide and <strong>the</strong>rmally decomposes <strong>the</strong> UO,<br />
to an average composition of U02.6. 'The charge<br />
is treated with H, to reduce <strong>the</strong> U02,6 to U02 and<br />
<strong>the</strong>n hydrofluorinated with H,-HF (approximately<br />
1O:l mole ratio) to convert <strong>the</strong> UO, to UF4. The<br />
progress of <strong>the</strong> reaction of 1J02 to form UF4 is<br />
followed by <strong>the</strong> changes in <strong>the</strong> liquidus tempera-<br />
ture of <strong>the</strong> binary mixture as <strong>the</strong> melting point of<br />
<strong>the</strong> charge decreases from <strong>the</strong> initial melting point<br />
of 845OC for <strong>the</strong> LiF to 49OOC for <strong>the</strong> UF4-LiF<br />
(27 and 73 mole %) eutectic product. Hydrogen<br />
fluoride utilization and water production are also<br />
indicative of <strong>the</strong> progress of <strong>the</strong> reaction. After<br />
MSR Program Semiann. Progr. Hept. Feb. 28, 1965,<br />
OHNL-3812, pp. 149-50.<br />
252<br />
E. L. Nicholson<br />
a final H, sparge to reduce impurities, such as<br />
iron and nickel fluorides, to metals and to sweep<br />
out dissolved HF, <strong>the</strong> salt is sampled, filtered,<br />
and stored in a product container. This process<br />
has been satisfactorily tested on a small scale,<br />
and <strong>the</strong> results indicate that <strong>the</strong> processing time<br />
will be about 15 days/batch.<br />
'Tentative plans are to make three 12-kg 233U<br />
batches of salt, which will be used for <strong>the</strong> major<br />
additions to <strong>the</strong> barren salt in <strong>the</strong> MSRE, and one<br />
7-kg 233U batch, which will be loaded into 60 en-<br />
riching capsules.<br />
EQUIPMENT AND OPERATIONS<br />
The scheiiiatic equipment flowsheet for salt<br />
preparation is shown in Fig. 26.1. The cans of<br />
U03, each containing about 500 g of uranium, will<br />
be transported in a shielded cask from <strong>the</strong> 233U<br />
storage Bcility in Building 3019 to <strong>the</strong> TURF<br />
building (7930) and introduced into cell G. All<br />
operations in cell G will be done remotely. k?y <strong>the</strong><br />
use of manipulators, <strong>the</strong> cans will be loaded into<br />
<strong>the</strong> alpha-sealed can opener and <strong>the</strong> dunipei box,<br />
which discharges <strong>the</strong> oxide into <strong>the</strong> heated nickellined<br />
8-in.-diarn by 3-ft-high reaction vessel and<br />
routes <strong>the</strong> empty cans to storage for subsequent<br />
removal from <strong>the</strong> cell. The 'LiF is charged to<br />
<strong>the</strong> reaction vessel via <strong>the</strong> dumper. Process<br />
gases are supplied from outside <strong>the</strong> cell, and<br />
instrumentation is provided to control gas flows<br />
and processing temperatures. Waste gases are<br />
filtered to remove entrained 233U and scrubbed<br />
with KOH to remove unreacted WF before disposal<br />
to <strong>the</strong> radioactive off-gas system. After<br />
sampling, <strong>the</strong> product is transferred via a heated