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FFR_chap07.txt
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CHAPTER 7
DESIGN AND CONSTRUCTION OF EXPERIMENTAL
HOMOGENEOUS REACTORS*
7—1. INTRODUCTION
7-1.1 Need for reactor construction experience. The power reactor de-
velopment program in the United States is characterized by the construe-
tion of a series of experimental reactors which, it is hoped, will lead for each
reactor type to an economical full-scale power plant. Outstanding examples
of this approach are afforded by the pressurized water reactor and boiling
water reactor systems. The development of pressurized water reactors
started with the Materials Testing Reactor, followed in turn by the Sub-
marine Thermal Reactor (Mark 1), the Nautilug Reactor (Mark II), and
the Army Package Power Reactor. KExperience obtained from the construce-
tion of these reactors was applied to the full-scale plants built by the West-
inghouse Electric Company (Shippingport and Yankee Atomic Electrie
Plants) and Babeock & Wilcox Company (Consolidated Iidison Plant).
Although many have argued that the shortest route to economic power
will be achieved by eliminating the intermediate-seale plants, most experts
believe that eliminating these plants would be more costly i the long run.
To quote from a speech by Dr. A. M. Weinberg [1], while discussing large-
seale reactor projects: “The reactor experiment—a relatively small-scale
reactor embodying some, but not all, the essential features of a full-scale
reactor—has become an accepted developmental device for reactor tech-
nology.”’
An alternative to the actual construction of experimental nuclear reactors
has been proposed which consists of the development of reactor systems
and components in nonnuclear engineering test facilities, zero-power critical
experiments, and the testing of fuel elements and coolants in in-pile loops.
This approach, although used successfully in the development of various
solid-fuel coolant systems, is not completely applicable to circulating-fuel
reactors because of the difficulty of simulating actual reactor operating
conditions in such experiments. In in-pile loops, for example, the ratio of
the volume of the piping system to the volume of the reacting zone is never
quite the same as in a reactor, making it impossible to duplicate simul-
taneously the conditions of fuel concentration, enrichment, and power
density. In cases where these variables are important, the m-pile loops
*Prepared by J. A. Lane, with contributions from 8. E. Beall, 5. I. Kaplan, Oak
Ridge National Laboratory, and D. B. Hall, Los Alamos Scientific Laboratory.
340
7-2] WATER BOILERS 341
an at best provide information of an exploratory nature which must be
verified In an operating fluid-fuel reactor.
A second aspect of circulating-fuel reactors, which precludes relying
solely on engineering tests and in-pile loops, is the close interrelation of the
nuclear behavior and the operational characteristics of the fuel circulation
system, which can be determined only through construetion and operation
of a reactor. Other aspects of reactor design that can be best determined
nm an operating homogeneous reactor are continuous removal of fission
products produced in the nuclear reaction and remote decontamination
and maintenance of reactor equipment and piping.
7-1.2 Sequence of experimental reactors. It is obvious from the fore-
going that the construction of a sequence of experimental reactors has been
an important factor in the development of homogeneous reactors. In this
sequence, which started with nonpower rescarch reactors, seven such
reactors have been built (not mecluding duplicates of the water boilers).
These are the Low Power Water Boiler (LOPQO), the High Power Water
Boller (HYPO), the Super Power Water Boller (SUPQ), the Homogeneous
teactor Iixperiment (ITRIE-1), the Homogencous Reactor Test (HRE-2),
and the Los Alamos Power Reactor Experiments (LAPRE-1 and -2).
[ the sections of this chapter which follow, these reactors are deseribed
m detail, and their design, construction, and operating characteristics are
compared. Their construction covers the regime of homogencous reactor
technology involving the feasibility of relatively small reactors fueled with
aqueotls =olutions of urantum. Since their construction and operation does
not include svstems fueled with aqueous suspensions of thorium oxide
and or uranium oxides necessary for the development of full-scale homo-
geneous breeders or converters, additional experimental reactors will un-
douhtedly he built.
7—2. Warter BoiLers*
7-2.1 Description of the LOPO, HYPO, and SUPO [2-4]. Interest in
homogencous reactors fueled with a solution of an enriched-uranium salt
was initiated at the Los Alamos Scientific Laboratory in 1943 through an
attempt to find a chain-reacting system using a minimum of enriched fuel.
The first of a sequence of such reactors, known as LOPO (for low power),
went critical at Los Alamos in May 1954 with 565 grams of U2?5 as uranyl
<ulfate. The uraniun, containing 14.5%, U35 was dissolved in approxi-
mately 13 liters of ordinary water contained in a type-347 stainless steel
sphere 11t diameter and 1/32 . in wall thickness. The sphere was sur-
*Prepared {rom reports published by Los Alamos Scientific Laboratory and
other sources as noted.
342 IXPERIMENTAL REACTOR DESIGN AND CONSTRUCTION [cuHap. 7
rounded by beryllium oxide as reflector in order to minimize the eritical
mass of the U235 The lack of u shield and cooling system limited the heat
power level of LOPO to 50 milliwatts. A cross-sectional drawing of the
LOPO is shown m Iig. 7-1.
Iollowing successful low-power operation of the LOPO, the reactor was
provided with a thicker sphere (1/16 in.), integral cooling coils, and «a
shield to permit operation at 6 kw. Also, part of the beryllium oxide
refiector was replaced by o graphite thermal column, and holes through
the shield and reflector were provided for experiments. The eritical mass
of the modified reactor was 808 grams of U235 as uranyl nitrate at 14.09%
enrichment, contained in 13.65 liters of solution. The change from uranyl
sulfate to nitrate was made because an extraction method for the removal
of fission products was known only for the latter solution at that time. The
modified reactor, called HYPO (high power), went critical i December
1944 and operated at a normal power of 5.5 kw, producing an average
thermal-neutron flux of 10! neutrons/(em?)(sec). The temperature of
the solution during operation reached 175°F with cooling water (50 gal /hr)
at 46°1.
Since higher neutron fluxes were desired, as well as more rescarch facilities
than available from HYPO, the reactor was further modified and renamed
SUPO (super power water boiler).
The modifications were made in two parts. The first phase, begun 1n
April 1949 and completed in ebruary 1950, improved the experimental
facilities and increased the neutron flux. The second phase, begun in
October 1950 and completed in March 1951, increased the thermal neutron
irradiation facilities, improved the reactor operation, and removed the
explosive hazard in the exhaust gases.
The first group of alterations consisted of the following:
(1) The space around the reactor was increased by enlarging the building
so that experiments could be carried out on all four sides instead of only two.
(2) The construction of a second thermal column was made possible by
eliminating a removable portion of the reactor shield. This made available
a neutron beam and irradiation facilities on a previously unused face of the
reactor.
(3) The entire spherical core assembly was replaced as follows:
(a) Three 20-ft-long, 1/4-in.-OD, 0.035-in.-wall-thickness stainless
steel tubes replaced the former single cooling coil. This inereased the
operating power level from 5.5 kw to a maximum of 45 kw.
(b) A new removable level indicator and exit gas unit was mstalled
in the sphere stack tube. The stack tube itself was made more accessible
for future modifications.
(¢) External joints were not welded, but unions of flare fittings
were used to simplify the removal of the sphere or permit pipe replacements.
T 2] WATER BOILERS 343
Overflow
Cadmium
Safety Curtain Level
Electrode
Safety Cd Control Rod
Electrode
Upper Pipe
Stainless Steel Sphere
Containing Enriched
Uranyl Sulfate (UO 950 4)
Be O Reflector
Graophite Reflector
Level Electrode
Air Pipe
-\D
Basin
L ump
Fig. 7-1. Cross section of LOPO, the first aqueous solution reactor.
(i An additional experimental hole was run completely through the
reccctor tangent to the sphere. This 1is-in-ID tube supplemented the
I-in-1D “glory hole” running through the sphere.
4 The beryllium portion of the reflector was replaced by graphite.
The wll-graphite reflector gave a more rapid and complete shutdown of the
reactor and eliminated the variable starting source produced by the (y,n)
reaction on beryllium. A 200-millicurie RaBe source placed in the reflector
was used as a startup neutron source,
(5) Two additional vertical control rods were added which moved into
the sphere in re-entrant thimbles. These consisted of about 120 grams
of sintered B m the form of 9,/16-in. rods about 18 in. long. These
rods gave the additional control required by the change to an all-graphite
reflector. Previously observed shadow effects were eliminated by the m-
ternal position of the rods and by the location of the control chambers
mnder the reactor.
i1 The reactor solution was changed from 159, U235-enriched uranyl
nitrate to one of 88.79; enrichment. This made possible the continued use
of a low uranium concentration m the solution with the poorer all-graphite
retlector. The gas evolution produced by nitrie acid decomposition was
creathy reduced, due to the lower total nitrogen content.
344 EXPERIMENTAL REACTOR DESIGN AND CONSTRUCTION [cHAP. 7
(7) The entire inmer reactor shicld was improved to permit higher power
operation with o low neutron leakage and also to inerease the neutron-to-
gamma-ray ntensity in the thermal columns. Cadmium wus replaced by
B4C paratiin and additional steel shielding was added.
After operating the reactor with the above modifications for about 10,000
kwh at a power of 30 kw, the following (second group) alterations were
made:
(1) The original south thermal column was completely rebuilt
improved shielding to provide many more irradiation facilities,
(2) A recombination system was construeted to handle the off-gases from
the reactor. The use of a closed circulating gas system with o catalyst
chamber of platinized alumina removed any explosive hazard in the ex-
haust gases due to the presence of hydrogen and oxygen. The operating
characteristics of the reactor were greatly improved by returning dircetly
back to the reactor as water all but a very small fraction of the gases
produced.
(3) A shielded solution-handling system was constructed to simplify
the procedure of routine solution analysis and for the removal or change of
the entire reactor solution.
The average neutron flux in the SUPQO during operation at 45 kw is
about 1.1 X 10" neutrons/(cm?)(sec), and the peak thermal flux (in the
“glory hole”) 18 1.7 X 10'2 neutrons/(em?)(sec). Fstimated values for the
maximum intermediate and fast fluxes at 45 kw are 2.8 and 1.9 X 102 neu-
trons/(em?) (see), respectively. Calculations made from fast beams emerg-
ing from the north thermal column at this same power level gave the fol-
lowing fast-flux values above 1 Mev in units of neutrons/(em?2)(sec):
(1) at sphere surface, 1.1 X 10'%; (2) at bismuth column, 7 X 10'%; and
(3) at a graphite face 1 ft in front of the bismuth column, 2 X 10%.
The production of hydrogen plus oxygen due to radintion decomposition
amounts to approximately 20 liters/min during operation of the reactor at
45 kw. These gases leave the reactor core and pass through a reflux con-
denser which removes much of the water vapor and then through a stainless
steel-wool trap for final moisture removal. A blower feeds the gas into one
of two interchangeable catalyst chambers containing platinized alumina
pellets. These chambers, operating at 370 to 470°C, recombine the hy-
drogen and oxygen, and the gas leaving the catalyst contains the water
rapor formed. A second condenser reduces the temperature of the exit
gas to that entering the catalyst chamber. A total of 100 liters/min of gas
1s eirculated continuously in the closed gas system at pressures slightly
above atmospheric, and the hydrogen concentration is kept below the
detonation limit at all points of the system. Excess pressures produced in
the gas system can be bled to the atmosphere through a 150-ft-high exhaust
stack.
with
y
7-2]
WATER BOILERS
345
The characteristics of LOPO, HYPO, SUPO, and the North Carolina
State College Water Boilers are summarized in Table 7-1.
DEsioN CHARACTERISTICS OF WATER BOILERS
TasLE 7-1
LOPO HYPO sSUPO NCSR [5]
Power level, kw 5 X 1072 5.6 45 10
Solution (111 HQO) IYOQSO:{ UOz(NO'})z IYOQ(NO3)2 UO2SO4
U235 wt., grams 765 870 870 848
- Solution volume, 13 13.65 13.65 15
hiters
- Enrichment, % 14.6 14.0 88.7 90
AMaximum thermal- | 3 x 109 2.8 X 101 1.7 x 1012 5 x 101
neutron flux
Reflector material BeO Be and Graphite Graphite
graphite
Coolant flow rate None 50 180 240
gal hr
Solution tempera- 39 85 85 &0
ture, °C
Experimental None 1 thermal 2 thermal 1 thermal
facilities column columns {'glory column
hole” and 12 exposure
tangential hole) ports
7-2.2 Kinetic experiments in water boilers. In August 1953, experi-
ments were performed on the SUPO by a group of scientists from the Oak
Ridge National Laboratory and Los Alamos [6,7] to determine the degree
to which a boiling (and nonboiling) homogeneous reactor automatically
compensates for suddenly imposed supereritical conditions. Previous
boiling experiments in 1951, unreported in the open literature [8], had
indicated the stability of SUPO under steady-state boiling conditions;
346 EXPERIMENTAL REACTOR DESIGN AND CONSTRUCTION [CHAP. 7
however, there remained considerable doubt as to the adaptability of a
reactor of this type to a sudden introduction of excess reactivity such as
might occur with a sudden inercase in pressure above the reactor. The
tests were performed by suddenly ejecting a neutron poison, consisting of
an aluminum rod containing boron carbide at its tip, and simultaneously
meaguring the neutron flux level with high-speed recorders connected to
a boron-coated ionization chamber located in the graphite reflector. The
amount of reactivity introduced was determined by the position of a
calibrated control rod. Although the experiments were interrupted by
frequent accidental serams, caused by the unsuitability of SUPO to boil-
ing at high solution levels in the sphere, the results indicated that both
boiling and nonboiling solution reactors are capable of absorbing reactiv-
ity inereases of at least 0.495 kg added in about 0.1 sec. In both boiling
and nonboiling eases, the reactor power was self-regulating, but excur-
siong were terminated more rapidly under boiling conditions. The average
lifetime of prompt neutrons in the reactor was caleulated from the initial
prompt rise in the neutron flux and found to be about 1.7 X 107 * sec.
Following a reactivity addition, the initial rate of reactivity decrease
(0.2 sec after start) was greater than about five times the rate which could
be attributed to core-temperature rise and the associated negative tempera-
ture coeflicient (0.0249 k/°C). As the gas bubbles left the core region,
reactivity decrease due to core-temperature rise Increased I relative
importance.
More recent experiments with the Kinetiec Experiment for Water Boilers
(KEWB-1), operated by Atomics International for the U. S. Atomic
Energy Commission [Y], have verified the self-controlling features of a
solution-type reactor. It was found that automatic shutdown due to the
temperature increase and formation of gas bubbles in the reactor fuel
solution occurs under all abnormal operating conditions tested.
7-2.3 The North Carolina State College research reactor [5]. The sim-
plicity of the Water Boiler reactor has made it of interest as a laboratory
tool for experimental work with neutrons and gamma rays and also to
provide training in reactor operation, and ten such reactors were in opera-
tion or planned in the United States by the end of 1957. The first college-
owned nuclear research reactor, which started operating at 10 kw in Sep-
tember 1953 at North Carolina State College, Raleigh, North Carolina,
was of this type. It was completed after four yvears of planning, design,
and construction, at a cost of $130,000 for the reactor, plus $500,000 for
the reactor building and associated laboratory equipment. It differs from
the Los Alamos SUPO in that the fuel container is a cylinder 11 in. in
diameter and 11 in. high, rather than a sphere. Its experimental facilities
include 12 access ports and a thermal column.
p—
7-2] WATER BOILERS 347
In June 1955, the reactor was shut down because of leaks which developed
in the fuel container and permitted the radioactive fuel to contaminate the
inside of the reactor shield. After a major repair job, operation of the
reactor with a new core was resumed in March 1957 at a power level of
500 watts, and the reactor has operated successfully at that level for a year.
7-2.4 Atomics International solution-type research reactors. Several
versions of the Water Boiler are being offered commercially by various
companies. The major supplier is the Atomies International Division of
North American Aviation Company which has built, or is building, 11 such
reactors. Low-power reactors are: the l-watt Water Boiler Neutron Source
(WBNS) originally at Downey, California, which was moved to Santa
Susana and modified to operate at 2 kw; a new J-watt laboratory reactor
(L-17) for Atomics International; the 100-watt Livermore Research
Reactor at Livermore, California; and a 3-watt reactor planned for the
Danish Atomic Energy Commission at Risg, Denmark. Higher power
Water Boilers, operating at 50 kw, include the Kinetic Experiment for
Water Boilers (KEWB-1) at Santa Susana; the UCLA Medical Facility
at Los Angeles, California; and reactors for the Armour Research IFounda-
tion in Chicago, Illinois; the Japan Atomic Energy Research Institute at
Tokai, Japan; Farbwerke Hoechst A. G. at the University of F rankfurt,
" Reactor Core TR |
- %Concrem Shielding X
o )
o
Neutron Exposure Facilii;y_‘_‘
TR s
"Control Room - - \ _
Reactor Utili‘ty Room”
Fig. 7-2. Armour Research Foundation research reactor (courtesy of Atomics
International, a division of North American Aviation Co.)
348 EXPERIMENTAL REACTOR DESIGN AND CONSTRUCTION [cHAP. 7
West Germany ; the Senate of West Berlin (Institute for Nuclear Research),
Germany; and the Politecnico Enrico Fermi Nueclear Study Center at
Milan, Italy.
The first solution-type research reactor for industrial use went into
operation in June 1956. The general features of this reactor, which Atomics
International built for the Armour Research Foundation at the Illinois
Institute of Technology, Chicago, Illinois, are shown in Fig. 7-2.
The exposure facilities include one 6-in.-diameter beam tube extending
radially to within 2 ft of the core tank and 4 in. in diameter from there
to the core tank; two 4-in. and two 3-in. beam tubes extending radially to
the core tank; two 2-in. through-tubes passing tangentially to the core
tank; one 13-in.-diameter tube passing through the central region of the
core; four 4-in. vertical tubes located in the reflector; one 5 ft X 5 ft graphite
thermal column with a 12-in.-square removable section. The tube facilities
consist of steel sleeves extending through the concrete shield and aluminum
thimbles or liners which reach to the immediate vicinity of the core. Each
tube facility i1s equipped with a graphite reflector plug and a dense con-
crete-and-steel shielding plug to be installed when the facility is not in use.
The horizontal thermal column is formed by a 5-ft-square column of
graphite, in the center of which are nine removable graphite stringers. A
large volume which may be used for exposures is provided between the
end of the thermal column and the inner face of a movable concrete door.
The thermal column access ports open into this volume.
To take advantage of the 50,000 curies of gamma activity produced by
the fission-product gases circulating through the gas recombiner tank,
exposure facilities are provided which extend from the subpile room into
the exposure room and into the valve room. The facilities listed below
consist of steel sleeves and aluminum thimbles which extend through the
dense concrete walls of the exposure room.
2 gamma ports, 4 in. diameter
2 gamma ports, 8 in. diameter
1 rectangular gamma slot, 6 in. X 18 in.
In addition, two 4-in.-diameter gamma ports extend from the subpile
room into the valve room. As with the beam tubes, each port is equipped
with a plug to be installed for shielding purposes when the port is not in use.
7-3. Tae HomogeENEOUs REacTOrR ExpermMExT (HRE-1) [10-13]*
7-3.1 Introduction. In 1950 the Oak Ridge National Laboratory under-
took the task of designing, building, and operating a pilot-plant fluid-
fuel reactor, the Homogeneous Reactor Experiment (HRE-1), shown in
*Based on a paper by C. E. Winters and S. E. Beall [10].
7-3] THE HOMOGENEOUS REACTOR EXPERIMENT (HRE-1) 349
¥
STy
A
v
5
y
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Fia. 7-3. The homogeneous reactor experiment (HRE-1).
Fig. 7-3. The purpose of this reactor was to investigate the nuclear and
chemical characteristics of a ecirculating uranium solution reactor at
temperatures and powers sufficiently high for the production of electricity
from the thermal energy released. Specifically, it was designed to operate
with a full-power heat release of 0.6 to 3.5 million Btu/hr (200 to 1000 kw
of heat), and a maximum fuel-solution temperature of 482°F, yielding,
after heat exchange, a saturated-steam pressure of about 200 psi.
During the 24-month period in which the reactor was in operation,
starting in April 1952, liquid was circulated for a total of about 4500 hr.
The reactor was critical a total of 1950 hr and operated above 100 kw for 720
hr. The maximum power level attained was 1600 kw. The reactor was shut
down in the spring of 1954 and dismantled to make room for the Homo-
geneous Reactor Test (HRE-2), having successfully demonstrated the
nuclear stability of a circulating-fuel reactor. The characteristics of the
HRE-1 are summarized in Table 7-2.
7-3.2 The reactor fuel system. The reactor core consisted of a stainless
steel sphere 18 in. in diameter, through which was circulated 100 to 120 gpm
of 93% enriched uranyl sulfate dissolved in distilled water. The temperature
350 EXPERIMENTAL REACTOR DESIGN AND CONSTRUCTION [CHAP. 7
TABLE 7-2
CHARACTERISTICS oF HRE-1
Power, heat 1000 kw
Fuel U0:804 (939, enriched) in Ho0
Fuel concentration ~30 g U235 per liter (0.17 m UO2504)
U235 in core 1.5 — 2 kg
Core 18 in. diameter, stainless steel
Pressure vessel 39 in. ID, 3 in. thick, forged steel
Reflector 10 in. D20, pressurized with He
Specific power 20 kw/liter
Fuel inlet temperature 210°C
Fuel outlet temperature 250°C
System pressure 1000 psi (430 psi above vapor pressure)
Gas removal system Vortex flow through core
Radiolytic gas recombination CuSO4 (internal); flame and catalytic re-
combination (external)
Control system Reflector level, safety plates, temperature
control
Shielding 7 ft barytes conecrete
Stearn temperature 382°F
Steam pressure 200 psi
Electrical capacity 140 kw
rise of the solution passing through the core was about 72°F at a power
level of 1000 kw. The liquid was discharged from the core at a temperature
of 482°F, and cooled to 410°F by evaporating water from the shell side of a
U-~tube heat exchanger, thus generating about 3000 Ib/hr of 200 psi steam.
A canned-rotor centrifugal pump returned the fuel to the core to be re-
heated. The total volume of solution in the high-pressure system was about
90 liters, of which 50 liters were in the core. A schematic flow diagram of
HRE-1 is shown in Fig. 7-4.
A total pressure of 1000 psi was maintained in the fuel system by heating
a small volume of fuel to 545°F in a pressurizer chamber directly above the
sphere. 'The 1000 psi total pressure, which is over 400 psi greater than is
required to prevent boiling of the fuel solution, was necessary to minimize
the volume of decomposition gases.
7-3.3 The reflector system. The reflector of HRE-1 was a 10-in. layer
of heavy water surrounding the core vessel. The heavy water was pressur-
1zed with helium to within 4100 psi of the fuel pressure in order to minimize
stresses 1In the 3/16-in. wall of the spherical fuel container. Both the
reflector and the concentric core were contained in an outer pressure vessel
7-3] THE HOMOGENEOUS REACTOR EXPERIMENT (HRE-1) 351
To Stack ¢ Steom Drum
200 psi St
t o psi eum/
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e
Rod Drive Mechuanism 120 gpm 3
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Fission Gas 1 /s . '
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Pressurizer . o
2 1000 psi 250°C
Cold T e el supnies § [ AL
(-20°C) Storage Tun 1000 psi) 7
Condensate Weighing Tanks b3 Hydrogen-Oxygen ! s Generator
Flame Recombiner
Hydrogen, Oxygen,
Staam, and Fission Gases
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2 D0 Cooler
(ondener Neutron Absorhing
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High Pressure oo .
Reducing Valve® D,0 Druin Valve
i 2
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Condensote
15 osi . Return Valve
p 1000 psi (Close To 1000 psi
(. Concentrate ‘ 15 psi
{) Fuel Feed Pump Fuel) \’ DzoFeed Pump
F1g. 7-4. Schematic flow diagram, HRE-1.
of forged steel, 39 in. in inside diameter, with a 3-in.-thick wall. A 24-in.,
1500-psi standard ring-joint flange at the top of the vessel permitted
removal of the inner core.
In order to limit thermal stresses and to reduce corrosion of the steel
vessel, the reflector temperature was regulated near 350°I. About 50 kw
of heat conducted from the fuel core to the reflector liquid was removed by
cireculating the heavy water with a 30-gpm canned-rotor pump through a
reflector cooler which acted as a boiler feedwater preheater. A jet was
located in this high-pressure circulating loop, the suction of which drew a
continuous stream of gas from the vapor space above the reflector to a
catalytic recombiner so that the concentration of deuterium and oxygen
gases in this vapor space could be kept below explosive limits.
Some measure of nuclear control was obtained by changing the level of
the reflector. The level could be lowered by draining liquid through a valve
to storage tanks, or raised by starting a feed pump. This pump, which
emploved a hydraulically driven diaphragm with check valves, had a
capacity of approximately 2 gpm against 1000 psi. Its intake was connected
to supply tanks at atmospheric pressure, located below the reactor. These
tanks also served as degas chambers for the reflector liquid which was dis-
charged from the pressure vessel. Helium, water vapor, and D2 and O:
352 EXPERIMENTAL REACTOR DESIGN AND CONSTRUCTION [cHaAP. 7
gas liberated here passed upward through a condenser to a small low-
pressure catalytic bed where the ()2 and Do gases were recombined to D»O.
Cold traps operated at —20°I" were included in the reflector-system vent
lines to prevent the loss of D20 or its contamination with H20) vapor.
7-3.4 The fuel off-gas system. When the reactor was operating, with-
out copper sulfate in the fuel solution, the fuel solvent (H.O) was decom-
posed by the energy of fission to yield a stoichiometric mixture of hydrogen
and oxygen gas at a rate of 0.28 c¢fm (10 efm at STP). In addition to this
large volume of decomposition gases, there was also produced a very small
volume (20 ce/day) of intensely radioactive fission gus. If these gases had
not been removed and replaced by more liquid, excessive pressures would
soon result, and since virtually all of this gas was liberated within the core,
the displacement of fuel solution by the gas would make it impossible for
the chain reaction to continue. I'or this reason, the gas was continuously
separated from the fuel in the core by injecting the main circulating stream
tangentially near the equator of the sphere, which caused the fluid to rotate
and form a vertical cylindrical vortex approximately 1/4 1. in diameter.
The centrifugal action of the rotating fluid served to separate the decom-
position and fission gases from the liquid to the vortex, the axig of which
was aligned with the fuel outlet. A nozzle with a central opening in the
fluid outlet allowed the removal of gas from the vortex. This gas plus
about 0.8 gpm of the fuel solution was passed through the outer annulus of
a countercurrent, concentric-tube heat exchanger, which was partially
cooled by 0.8 gpm flow of fresh makeup liquid being pumped back to the
core. The cooled mixture of gas and liquid was then throttled through a
valve into a gas separator which was connected to the fuel-solution storage
tanks. The gas-steam mixture rose from the gas separator to a condenser
immediately preceding a flame recombiner, so that the gases leaving the
condenser were combustible and reunited to water in the flame of the re-
combiner shown in Fig. 7-4.
The flame recombiner is best described as an oversized Bunsen or Meeker
burner enclosed in a water-jacketed cylinder. In the HRE-I no attempt
was made to use this 40 kw of high-temperature heat, although in larger
scale reactors this energy might be used to superheat steam about 70°L.
The exit gases from the flame recombiner contained only fission products
and small amounts of unrecombined hydrogen and oxygen. They were
passed through a catalytic recombiner which contained a platinized alumina
catalyst to eliminate the traces of hydrogen and oxygen. Also, the catalytic
bed was used to react the entire gaseous output at low reactor powers when
insufficient gas was being liberated to maintain a steady flame at the burner
of the flame recombiner. The catalytic bed was followed by a condenser
and cold traps to prevent the loss of water from the system. The gas stream
7-3] THE HOMOGENEOUS REACTOR EXPERIMENT (HRE-1) 353
at this point was composed mainly of excess oxygen plus the highly active
fission gases, mainly xenon, krypton, and their decay products. The ac-
tivity of these gases was many orders of magnitude greater than the activity
which can be discharged directly to the atmosphere without the construc-
tion of a very expensive stack; therefore it was desirable to provide some
inexpensive means of storage for the dissipation of the radioactivity. This
was accomplished by passing the gases through cold traps to remove
moisture and adsorbing them onto water-cooled activated-carbon beds
which were buried underground outside the reactor building. It is estimated
that the equilibrium activity of the gases held on the carbon bed was 400,000
curies, *
The adsorption efficiency of the charcoal, even at ground temperature,
was good enough to prevent a discharge of activity greater than a few
curies per day. However, even this amount of activity had to be diluted
so that the atmospheric concentration at ground level was not greater
than 10718 curies/cc of air. Dilution was accomplished by feeding the
active gas into a 1000-cfm ventilating air stream from the reactor shield
and then to a 100-ft-high stack. During operation the gaseous activity
inside the stack barely exceeded inhalation tolerance.
7-3.5 Fuel concentration control. The condensate which was removed
from the vapor-gas mixture upstream of the recombiner was returned either
to the fuel storage tanks or to weighed holding tanks. The accumulation
of water in the holding tanks provided a means of increasing the concen-
tration of fuel in the storage tanks underneath the reactor. Since fuel was
pumped continuously from the storage tanks to the high-pressure system
by means of a duplex-diaphragm type pump at a rate of 0.8 gpm, it was
possible to vary the concentration of the fuel which circulated through
the reactor. Figure 7-5 shows how the core temperature varied with fuel
concentration, in g/kg HoO. Furthermore, since the operating temperature
of the core was controlled by the fuel concentration as shown in this figure,
the operator had a convenient means of adjusting the solution temperature
to the desired level. This feature of variable concentration was employed
during startup of the reactor when the concentration had to be changed
by large amounts, and also during steady operation for small changes in
temperature. When sudden dilution of the fuel was desired, as in the case
of a complete shutdown, the condensate holdup tanks were quickly emptied
through a drain valve into the fuel-storage tanks, or condensate was pumped
directly into the core.
The steep slope of the curve in Fig. 7-5—i.e., the large negative tempera-
ture coefficient—was a feature which was extremely important from safety
*One curie equals 3.7 X 101¢ disintegrations per second.
354 EXPERIMENTAL REACTOR DESIGN AND CONSTRUCTION [cHAP. 7
YT T T T T T T
40 |—
39—
38 }— |
37 |— ]
36— —
35—
34—
33—
32 |—
31—
30 +—
Fuel Concentration, g U235/kg H,0
29—
Theoretical - ~4— Experimental
28—
27}
26—
25—
gal
0 25 50 75 100 125 150 175 200 225 250
Temperature, °C
Fic. 7-5. Dependence of eritical fuel concentration on temperature in HRE-1.
and power-demand standpoints. Tor instance, a temperature rise of only
15°C was necessary to overcome a reactivity increase of 19, an amount
considered very dangerous in most solid-fuel reactors.
7-3.6 Power removal. The steam generated in the fuel heat exchanger
was fed to a conventional multistage condensing turbine generator rated
at 312 kva. With the reactor operating at 1000 kw and 250°C, a sufficient
quantity of steam at 200 psi was produced to generate about 140 kw of
electricity. Steam leaving the heat exchanger was first passed through a
time-delay drum with a radioactivity monitor at the inlet and a quick-
closing valve at the outlet to prevent the escape of activity into the turbine
system in the event of boiler tube failure. Small feed pumps returned the
condensate from the turbine to the boiler.
Upon increase in generator load, the turbine governor opened the
turbine throttle valves, increasing the steam demand, lowering the steam
7-3] THE HOMOGENEOUS REACTOR EXPERIMENT (HRE-1) 305
pressure and temperature, and reflecting itself into increased cooling of
the uranium solution, which automatically increased the reactivity of the
core and completely compensated for this increased load.
7-3.7 Internal-recombination experiments. The use of copper dissolved
in the reactor fuel for the complete recombination of radiolytic gas was
successfully demonstrated in the HRE-1 [14]. Copper ion was added as
copper sulfate on four occasions, increasing the copper concentration to
10, 25, 75, and 1509 of that necessary for complete recombination (i.e.,
6.6 g CuSOy4/liter) in a static system at 250°C, at 1000 psig total pressure,
and at a uniform power density of 20 kw/liter. The Investigation was
conducted at temperatures from 185 to 260°C, at pressures from 765 to
1200 psig, and at power levels as high as 1600 kw. In the main, the copper
behaved as expected from static bomb tests. The highest power level for
which all the gas was internally recombined was 1350 kw. In the course of
all copper experiments, including 350 hr of operation at the highest copper
concentration, 0.062 molar, no deleterious effects due to the presence of
copper were observed.
7-3.8 Nuclear safety. Although operating experience later verified early
predictions of the inherent safety of this reactor, at the time of design it
was considered judicious to incorporate conventional safety devices in the
reactor for protection against potentially dangerous situations which might
arise during low-power operation and until the dynamic stability had been
demonstrated by experiment. Safety measures in the order of their auto-
matic action as installed to limit reactor power or power doubling time
were:
(1) Two magnetically coupled safety plates, worth about 45 g of uranium,
which by falling in 0.01 sec caused the reactor temperature to be lowered
from 250°C to approximately 243°C.
(2) Dumping of the reflector.
(3) Dilution of the fuel (this was the normal shutdown procedure).
(4) Stopping of the steam extraction hy closing either a steam valve or
the turbine governor.
(5) Draining the fuel solution to the noncritical-geometry tanks below
the reactor.
IIxperiments demonstrated that the reactor was extremely fast-acting
with respect to limiting power surges and led to the belief that mechanical
control devices were unnecessary [15]. These consisted of a series of kinetic
experiments in which the power responses to reaetivity increases were
observed. Tirst, the entire range of normally available reactivity increases
—fuel concentration, rod withdrawal, and reflector level—was tested with
initial power levels as low as 10 watts and reactivity rates up to 0.05% per
356 EXPERIMENTAL REACTOR DESIGN AND CONSTRUCTION [cHap. 7
second. Then, in order to provide more drastic tests, the main fuel circu-
lating pump was stopped, the reactor was maintained at a low power and
at high temperature, but the heat exchanger was cooled about 100°C.
When the pump was restarted, the cold fuel from the heat exchanger was
rapidly injected into the core, producing a rate of reactivity increase of as
much as 0.8% k. per second. The results of two experiments in which
only the initial powers differed are shown in Fig. 7-6; the power increased
in a period as short as 35 msee, reaching a peak of 10 Mw in 1 see, and then
approached the equilibrium power demand within 0.2 sec after the peak.
The calculated pressure rise associated with the peak power of 10 Mw
was only 5 psi.
In these experiments the worst combination of circumstances was im-
posed on the reactor. It was successfully demonstrated that the HRE-1
was sufficiently stable to withstand nuclear transients greater than those
expected from operating errors.
7-3.9 Leak prevention. A major problem in the HRE-1 was to main-
tain absolute leaktightness in all components. The radioactivity of the
solution during operation was about 30 curies/ce. Twenty-four hours
after shutdown the activity was about 3 curies/ce. With these high
activities, the total leakage from the system had to be kept below 1 cc per
day. A much better performance than this was attained through the use
of canned-rotor pumps, double tube-sheet exchangers, and bellows-sealed
valves.
All welded joints were made with extraordinary care and tested by sev-
eral nondestructive methods before being approved for use. Flanged
joints were assembled with stainless steel ring gaskets of oval cross section
TABLE 7-3
HRE-1 ConsTrUcTION CoOST SUMMARY™
Total %% of total
Building $ 300,000 27.5
Fuel and reflector equipment and piping 420,000 38.2
Instrumentation 190,000 17.6
Shield 110,000 9.7
Power system 80,000 6.9
Total construction cost for HRE-1 31,100,000 100.0