Professional Documents
Culture Documents
by
atthe
MASSACHUSETTS INSTITUTE OF TECHNOLOGY
May,1990
ay, 1990
Ccrtified by
is Cosupervisor
Certified by
Dr. Marvin M. Miller, Thesis Cosapervisor
Accepted by
Profesor Allan F. Ftenry,
Chairman, Committce on Graduate Students
MASSACHUSffTS INS11TliTE
OF Trr, '~V
NOV 1 :J 1990
LIBRARIES .AF~_ .. qVf:S'
Effects ofVariation of Uranium Enrichment
on Nucleazo Submarine Reactor Design
by
Thomas D. Ippolito J r.
Abstract
2
TabJe ofConteuta
Par:e
Abstract 2
List of Figures 6
List of Tables 8
Aeknowledgements 9
Disclaimer 10
Chapter 1. Introduction 11
1.1 Conventional Vs. Nuclear Propulsion 12
1.2 Submarine Pressurized Water Reactor Nuclear Power Plant 15
1.3 Design Cliteria and Objectives 17
1.4 Selection of Heactor Design Limita Z3
3
3.2 Fuel Element Design 71
References 181
4
Appendix A. Non-Proliferation Treaty and Foreign Nuclear
Objectives 187
5
Ust ofFigures
FifDire PaEe
1.1 Typical PWR plant. 18
1,2 Typical nuclear submarine propulsion system. 19
1.3 Technicatome's integrated PWR which powers France's ID
SSNs.
2.1 Correlation between fission gas release and fu.el center 48
temperatura for uo2 fuels.
3.1 Caramel fuel plate. Gl
3.2 Cermet fuel plate. ffi
3.3 Partial estimate of burnup Vs. U02 volume fraction. ffi
3.4 Schematic cross-sections of cermet dispersion systems. 70
3.5 Thick plate fuel element design. 'TJ
3.6 Assemblage of reactor fuel elements. 'TJ
3.7 Fuel element design window. 75
4.1 Interdependence of reactor design parameters. 85
4.2 Design space. 00
4.3a Design variations for reactor core ( 1). 00
4.3b Design variations for reactor cores (2,3,4,5), 91
4.4 EPRI~Cell data flow. 95
4.5 EPRI-Cell 3-D slab. 00
4.6 Fuel cell for reactor core (1). 100
4.7 Fuel cell for reactor cores (2,3,4,5). 101
4.8 Fuel element extra water. 105
4.9 Thermal flux distribution for reflected reactor. 118
4.10 Design procedure for reactor core (1). 1Z3
4.11 Design procedure for reactor cores (2,3,4,5). 124
4.12 Fuel plate temperature profiles. 132
5.1 Reactor core (1), k-effVs. time. 141
5.2 Reactor core (2), k-effVs. time. 142
5.3 Reactor cors (3), k-effVs. time. 143
5.4 Reactor core (4), k-effVs. time. 144
5.5 Reactor core (5), k-eff Vs. time. 145
5.6 Effects of gadolinia distribution on k-effVs. time. 146
5.7 Reactor core fuel element grids. 154
6
5.8 Reactor core (1), plutonium Vs. time. 159
5.9 Reactor core (2), plutonium Vs. time. 100
5.10 Reactor core (3), plutonium Vs. time. 161
5.11 Reactor core (4), plutonium Vs. time. 162
5.12 Reactor core (5), plutonium Vs. time. 163
B.1 Reflected criticai masses of uranium and plutonium Vs. 1.00
isotopic mix.
7
List ofTabJes
Tabl~ Pa.~
1.1 Submarine Power Requirements at 2670 tons displacement. 14
1.2 Design choices and limita for comparativa core neutron.
analysis studies. 28
2.1 Uranium bearing compounds. :Jj
8
Acknowledgments
The author wishes to express bis thanks to Dr. Marvin M. Miller who,
through the sponsorship of the MIT Center for Intemational Studies,
provided him with the opportunity to participate in this study and who also
provided valuable guidance throu~hout its duration.
He also thanks Ptofessor David D. Le.nning for his expert advice,
guidance and instruction with the many aspects and technical details of
nuclear reactor design and analysis encountered in this study.
A word of appreciation goes to Professor Ronald G. Ballinger with
whom the author consulted regarding the prolonged irradiation
performance of the various nuclear fuels considered.
Special thanks to Dr. Rachei Morton for her invaluable assistance wi th
setting up the computer link from MIT to Argonne National Laboratory.
The author expresses his sincere appreciation to Dr. William Woodruff
of the Engineering Staff of Argonne National Laboratory for bis guidance
with the use of the EPRI-Cell code and his many suggestions for the
application of EPRI-Cell to the reactor physics problems encountered. Dr.
Woodruff also provided much assistance with the IBM Job Contrai
Language needed to run EPRI-Cell. Also, thanks go to Fran Carneghi of
Argonne's Computing Services Division for her administration of the
computer account set. up to conduct this study.
The author must also thank those who provided him with much
encouragement and emotional support through this thesis and his three
years at MIT; his father, mother and grandmothers, and of course his
brother and sisters.
Finally, the author must give thanks to,
- the one who allowed him to come to MIT;
- the one who provided him with endless motivation;
- the one who was with him through the many sleepless nights
spent running EPRI-Cell, mak.ing figures and writing this
thesis;
- the one who made this thesis happen;
9
This study does not involve in any way, the use of classified material;
rather, it is derived from material that is published in the open literature.
10
CHAPTERl
Introduction
U .S. and British nuclear submarine reactors are fueled with very
highly enriched uranium; typically 97.3% in the U.S. case.[l] France,
however, has deployed SSNs fueled with low enriched uranium (LEU);
typically lesa than 10%.[2] (By convention, weapons-grade uranium
(WGU), higbly enriched uranium (HEU) and low enriched uranium (LEU)
are defined to be uranium wbich has a (]235 content of greater than 90%,
greater than 20% and lesa than 20% respectively.) Since the {:ritical mass
increases rapidly below 20%, LEU is considered to be lesa of a proliferation
concem than HEU, although more plutonium is produced in an LEU fu.eled
reactor. For this reason, it is generally easier to purchase LEU on the
intemational market, reducing the argument for the need to develop
indigenous enrichment capability. Relevant here is the fact that more than
half of the separative work of the enrichment process required to produce
HEU has been done in producing LEU .[3]
t AB distinguished from SSBNs which are both nuclear powered andare also armed with
nuclear-tipped ballistic missiles.
11
The purpose of this study is to assess the tradeoffs involved in the use of
HEU Vs. LEU as an SSN reactor fuel, with regard to such factors as core
life, core size, and reactor safety. This has been accomplished by modeling
one HEU and an two LEU reactor cores for comparison<
where,
12
requirement can increase by as much as 40%.[ 4]. One should note the
propulsive power increases with the cube of the forward velocity.
'.rhe Rubis can be considered to be an intermediate size submarina
whose volume displacement and total power requirements will serve as a
design basis. Submarine submerged volume displacements range from the
1070tons (1070m3 )West German Vastergotland class diesel powered
submarin~ or SSK, to the 8400tons (8400m3) ofthe British SSN, HMS
Resolution.[6]
Naval submarines must be able to take evasive action requiring high
speeds of25-30 knots or greater. Since an SSK runs submerged on
electricity produced by diesel generators and stored in batteries, this can
only be achieved for a short period of time; typically 1 hour maximum. This
is due to the tremendous propulsive power requirements which rapidly
deplete the batteriea.[5] SSKs can maintain an average speed of about 13
knots submerged.[6] The higher the average speed, the higher the
"indiscretion rate" or the percentage of time that the submarine must
surface to snorkel. In doing so, an SSK is highly vulnerable to radar
detection, visual detection and attack by surface ships, aircraft and other
submarines.
By contrast, most SSNs can maintain an average speed of25-35 knots
without approaching the surface. SSNs have an underwater endurance
which islimited only by the endurance ofthe crew. The SSN can thus
make high-speed, long distance undetected transite from one part of the
world to another. Only SSNs are capable of traveling under the Polar Ice
Cap, through the N orthwest Passage and in to the Arctic Ocean.
13
Table 1.1 Submarine power requirements at 2670 tons displacement
[adapted from Reference E]
14
1.2 8ubmar.IDe Pnaurized Water Reactor Nuclear Power Plant
15
1) A shielded radioactive compartment containing the reRctor, a
pressurizer, a steam generator anda primary coolant pump.
16
firm, Technicatome, and employed in alt ofFrance's SSNs, Figure 1.3. In
this design, the reactor, eteam generator, and primary coolant pump are
integrated into one steam producing unit eliminating component
separation and the large diameter interconnecting primary loop piping.
17
1 1111 STEAM
(TO TUHOINE~ l SECONDAHY
f LOP
I ._ FEEDWATER
CONTAOLS
fFROM
CONDENSERt
......,._STEAM GENEAATOA
-
00
! 111
CORE
SHROUD-t:
1 ~-11114 I
OOWNCOMER
---PAIMAAY LOOP
1
VESSEL~
REACTOR \ -- ~ I --- PUMP
WATER
CONTAO L CLUTCH
ROO ELECTRICAL
PROPULSION
Steam
Generator
Au:xiliary
Primary
Circuit
Auxiliary
Primary
Circuit
20
3) It was assumed that no shuftling of the mel elements would take
place in order to extend fuel humup. At the end of core life, fuel
elements near the center of the core are depleted more than those
in the outer region of the core. In a fuel shuftling operation,
some of the fuel elements near the outer regions of the core are
switched with fuel elements near the core center. Consequently
the total available reactivity ofthe coreis increased. Reactivity is
defined in Appendix C. Fuel bumup ia discussed in Appendix D.
21
2) Estim.ates of the safety parameters such as the Doppler, void and
temperature coefficients of reactivity as a function of enrichment
and quantity ofburnable poison, Gd203, present in the reactor.
These results can be used as a basis for deciding if selected cases should
be calculated in more detail, inclucling distributed bumable poison and/or
enrichment for power flattening and better bumup; control movement
reactivity and power peaking effects, and thermal-hydraulic considerations.
Power flattening involves the reduction of the peaking factor which is
described in Section 1.4.
Upon reaching the above outlined objectives, conclusions can be drawn
about the effects, i f any, of using LEU as a fuel instead of HEU, on
submarine design and operation. For example, if the LEU cores were
found to be significantly larger than the HEU core for a given reactor
power, a larger hull may be needed for the LEU fueled submarine
compared to the HEU fueled submarine . Based on the discussion of Section
1.2, this will reduce the submarines maximum forward velocity. Also, if
the unshu.tned LEU core lifetimes are shorter than that of the unshuffied
HEU core (the HEU core lifetime may, in some cases, be as longas the
submarine lifetime), the submarine must retum to port for fuel shuffiing
or refueling. These are major operations that for many submarine designs
require cutting open the hull, thus increasing the time the submarine will
be out of service. Submarine designers have generally avoided the use of
22
hatches dueto sealing problema at large depths.[lO] However, the French
Rubis does use large hatches to refuel.
23
be analyzed here was set at IOOOkW/1 and for the LEU reactors was set at
about IOOkW/1. The 93% enriched, U02 fueled Advanced Test Reactor at the
National Reactor Testing Station operated by ldaho National Engineering
Laboratory has a maximum operating power density of about 2600kW/l.[ll]
Com.mercial PWRs fueled with LEU of about 3% ave:rage enrichment,
operate with a maxi.mum power density of al:-out 250kW/l. To be
conservative, the maximum power densities to be applied to these
calculations were reduced. For each reactor design to be considered for this
study, a minimum average power density limit (q"'ave) was set at 50kW/l in
order to ensure the ability ofthe reactor to produce steam. The average
power density in a commercial BWR is about 56kW/l.
Another important dcsign parameter that was estimated for purposes
of this study is the ratio of the maximum heat generation rate to the
average heat generation rate or more simply, the power peaking factor (!l).
111
q max
0 = -..-,-
q ave
(1.2)
enrichment value of97.3% was selected since U.S. and British SSNs are
24
fueled with uranium of this enrichment. U.S. SSN reactor cores are reported
to have refueling httervals greater than 12 years, while future designa are
aimed at refueling intervals approaching 20 years, or the service lifetime of
the submarine.[2] Thus for the HEU core to be analyzed in this study, the
design operating lifetime without fuel shu.ffi.ing or refueling, was set at 20
years. These refueling intervals are based on a submarine service time of 240
days per year at sea while operating at an average of 26% of full power, or 60
full power days per year (60 FPD!Y). As deduced from Equation 1, this
representa about 63% of the maximu.m velocity.
25
dfferences in submarine design and operation between submarines fueled
with HEU and those fueled with LEU. Thus an LEU core also with a
refueling intervaJ of 20 years needed to be modeled. As a result, feasibility
calculations were done for a reactor core of 20 year operating life and fueled
with uranium enriched to 20%.
Throughout a reactor core lifetime (beginning-of-life(BOL)- endnof-life
(EOL)) the total available reactivity swings from some maximum design
value to some minimum design value at which the reactor can no longer
operate. The maximum design value is determined by the total possible
negative reactivity that can be inserted by control roda. The minimum
design value is set at some point above zero readivity in order to
compensate for the buildup to some maximum value, of the neutron
absorbing isotope Xel 3 7 upon shutdown of the reactor. This isotope results
from the decay of certain fission products. The maximum and minimum
design reactivity values that have been conservatively estimated based on
consideration of existing reactors, corresponds to values of ~rr = 1.24 and
kerr = 1.04 respectively. The terms reactivity and kelf are defined in
Appendix C.
During the operating lifetime of a reactor core, the maximum
permissible materials-limited fuel burnup may be reached before the
minimum design reactivity value. At this point, structural integrity of the
fuel element may not be assured if the fission process were allowed to
continue. This results from fission gas pressure buildup (i.e., some fission
products are gases) and irradiation damage to the fuel matrix. For the fuel
element design used in the LEU cases, the materials-limited fuel bumup
limit is estimated to be 60,000MWd!r.[l3] The burnup limit for the fuel
element design used in the HEU case will be further discussed in Chapter 5.
26
neutronics data provided by the EPRI-Cell code, it will be possible to
calculate with accuracy sufficient for this study, the information outlined
in Section 1.3.
The design choices and assumed limita are summarized in Table 1.2.
27
Table 1.2 Design choices and limits for comparative core neutron
analysis studies.
28
Nuclear reactor fuel elements consist of a ayatem of interacting
materiais that includes the fuel material, clad material and and in moat
cases a reactivity control material (i.e., burnable poison). For the optimum
performance required of an SSN reactor as described in Chapter 1, small
size, high power density and marimum refueling lifetime, this system of
materiais must allow good neutron economy. maximum fuel bumup, and
corrosion resistance. This system must attain these goals while subject to
the environment encountered in the PWR core described in Section 1.2
which includes high neutron Ouxes (at high energies) as well as high
operating temperatures, system pressures, thermal gradiente and heat
flu.xes. Also of great importance ia the chemical compatibility of the fuel
element materiais with respect to each other and to the reactor coolant (i.e.,
H20). This taystem of materiais must also be capable of withstanding
transient and ofr-normal conditions without failure and muat retain
coolable geometry during accident conditions such as a LOCA (loss-of-
cooling-accident) or LOFA (loss-of-flow-accident).
A fuel element composed of a given set of materiais may meet a given
set of performance objectives for a given set of reactor operating conditions.
However, the fuel element may be entirely inadequate when exposed to a
different reactor environment. For example, a particular fuel element may
perform satisfactorily in a low temperature research reactor used for the
production of neutrons but may melt or rapidly corrode when exposed to the
relatively high operating temperatures of a central station power
generating reactor or an SSN propulsion reactor. Thia fuel element may be
29
even lesa attractive for use or in a reactor cooled with a fluid other than
H 20. The final materiais seleetion process ia more or lesa a compromise
between the varioua in-reactor operating propertiea and characteriatica of
the fuel element materiais that resulta in a combination that most cl~Ge~J
30
2.1.1 Fuel Selectlon Criterta
The fuel material muat be carefully chosen in order fcr the fuel e!ement
to meet the SSN reactor fuel element deaign objectivea of maximum
bumup, JDllldmum operating lifetime, corrolion reaiatance and ability to
I
2) The fue! material should have only one crystal structure witlnn
the ope:rating temperature range of the reaetor (i.e . room
temperatura to maximum operating temperature). Chang~s in
crystal structure are usually accompanied by a volume change
that can damage the fuel element.
31
3) To preserve fuel element integrity du.ring the attainable lifetime
of tbe fuel element (based on fuel mecbanical behavior fuel
material or available reactivity in the fbel elementa), the fuel
material ahould be chemically and metallurgieally inert 'llith
reapeet to the reactor coolant and fuel element cladding.
32
6) The fuel material ahould permit maximum uranium loading per
unit volume of fuel. An enrichment limit impoaed on the
uraniu.m fuel producea two effects which muat be conaidered.
Lowering the uranium enrichment resulta in the addition of U238
which reducea the reactivity of the fuel element even if the
amount of 1J236 can be kept the same. Further. the added U238
reduces the allowable loading or concentration of U236 in the
reactor fuel el~~l:l~nta. For many reactor fu.el element designa,
use of LEU will aufficiently lower the initial reactivity so as to
render the use of the fuel element impractical. This will be
discussed further in Chapter 3. It should be noted that there are
three ways to regain reactivity lost by the use ofLEU: (1) the use
of higher uranium-loading fuel, (2) the use of a higher
performance reflector material, and (3) incease the core size. Of
courae a combination of these approaches can be userl.[12.]
33
The followi.ng aection review1 the fuel typea that have been considered
for use aa an SSN reactor fuel botb in the paat and for the purpoaea or this
study. The ceramic and metallic compounda of uranium. that were
considered are listed in Teble 2.1. The alloys ofuranium tbat were
considered Cor use aa nuclear fu.els are liated in Table 2.2. These tables are
by no meana emaustive.
The ideal uranium fuel ie the metal itself snce it has th(: hlghest
uranium maes density or uranium loading possible, (18.9 glcm3). Its high
thermal conductivity oC 35 W/m K allowa a fuel maximum temperature on
4
the order of 500C for the fuel element designa considered for this study.
This offsets the relatively low melting point (1130C) of uranium metal.
Other fuel types such as ceramic oxides may require maximum fuel
temperatures approaching 1000C in order to achieve the necessary heat
flux required to produce a coolant outlet temperature of 320C.
A major drawback to the use of uranium metal is that it has three
crystalline structures that are stable in the range of fuel temperaturee that
can be encountered in the reactor. This includes the norml operating
temperature range and temperature increases that can occur in transient
or accident conditions. Uranium metal undergoes a phase change at 661C
from alpha-uranium to beta-uranium and at 769C from beta-uranium to
gamma-uranium. Alpha-uranium has an orthorhombic crystal structure;
beta-uranium a tetragonal crystal structure and gamma-uranium a body-
centered-cubic crystal Gtructure. A volume increase accompanies the
34
Table 2.1. Uranium bearing compounds.
Thermal Thermal
Uranium Microscopic Macroscopic
Thermal Abaorption Ahaorption
Uranium Melting Denaity Ursmium Mua
Bearing Point Denaity Fraction Conduct Cross- C roas-
(W'cm 3) ivity Section of Seetion of
Compound (o C) (glcm 3) (wt'f,)
(For lOO'f, (W/m-K) Second Second
enriched) Element, Element,
oa (barns) Ea (em 1)
35.0
u 1133 18.9 18.9 100 (at4000C) - -
UAI 2 1500 8.1 6.6 81.5 0.23 0.086
UAI3 1350 6.7 5.0 74.6 0.23 0.098
UA1 4 7:1) 6.0 4.1 68.3 0.23 0.106
21.6
uc 2500 13.6 13.0 95.6 (to 1()()(ffi)
0.0032 0.00048
10.6 82.4 35.0 0.0032
uc2 =2500 12.9 (to l()()()OC) 0.(X.l802
35
Table 1.1. Uranium rich alloya.
Thermal Thermal
Microacopic MacroDeOpic
Uranium Meltini Denlity Uranium Uranium Thermal Abtorption Amorption
Beari.og Point c.'em 8) Denlity Mau Coaduet- Cro11 CrOII
Practioa ivity Section~
Alloy (oC) (Wcm a> Section of
(wt.11t) (W/m-K) Second Second
Blement. Element,
era (barna) :ta (em -1)
U -10wt.4MCl 11fJO 17.33 16.87 9) 28 2.6 0.267
uM 10wt.--,.,Nb (SoUdull)
J.3X)
16.68 1&.12 9) 1.1 0.133
11.36
U -10wt'~Zr (Sol.ichu) 15.76 14.25 00 0.027
0.18
U-76wt.,Al 1106 3.93 1.36 3)
0.23 0.132
(Bolidul)
36
not a satisfactory fuel for use in tbe power produci.ng PWRs conaidered for
thie atudy.
37
ueecl where the alphalbeta tranaform.ation temperature has been
raieed by alloying additiona.
38
incapable of meeti.ng the performance objectives of the SSN reactor designa
conaidered in thia atudy.[ 12]
A disadvantage to the use ofmolybdenwn ia that it has a relatively high
macroscopic neutron abeorption croaa-eection (I.,) of 160 cml~ (see Table
2.4), that may sufliciently lawer the available reactivity of a fuel element
using LEU ao as to prohibit its use in a modem SSN reactor core.
The uranium-niobium and uraniwn-zirconium alloys described in
Table 2.2 provide uranium loadinga of 16.68glcm.S and 15. 76g!cm3
respectively. As with uranum-molybdenu.m alloys, fission gas swelling at
2-4at% burnup are prohibitively high at temperatures greater than 400C.
Thus these fuels are also incapable of meeting the performance objectives of
e modem SSN reactor. It should be noted that at lower temperatures
uranium-molybdenum alloya are more resistant to swelling than uranium-
niobiu.m and uranium-zirconium alloys.
As in the case of malybdenum, niobiu.m has a relatively high l:a (60 cm-1)
and will also lower the reactivity of a fuel element using LEU. Zirconium,
however has the advantages of a relatively small I.a (9.8 cm-1) high melting
point ( 1845C), excellent ductility and good resistance to aqueous corrosion.
It is interesting to note that uranium-zirconium alloy fuels were used in
the early nuclear submarine program.[l6] At that time submarines did not
require the refueling lifetimea of modem SSN s.
Although uranium rich alloy fuels appear to be unsuitable for use in
the plate type fuel elements considered for thls study, they can be used in
rod type fuel elementB where there exista a sufficiently large gap between
the outer fuel surface and the claddinc inner surface to accommodate the
excessive swelling. During operation, fission gas swelling increases the
original fuel volume by roughly 20% at which the fuel contacts the cladding.
39
At thia point, aufficient numben of fiaaion gas bubblea present on the fuel
grain bound.ariea 1ink together to form a continuous path which allowa for
fislrion gas relea.se and preventa additional swelliug. The released gasses
collect in a plenum or void element at the top of each fuei element.
A large fuellcladding gap requirea a highly conducting medium such
as liquid sodium in order to prevent escessive fuel temperatures. Due to the
violent aodiumlwater reaction that will OCC1n in the event of cladding
rupture, water can not be used as the reactor coolant. Thus the reactor
must be cooled by liquid sodiu.m. In the 1C50s U.S. Navy Admirai Hyman
Rickover prevented the liquid metal cooled reactor (LMR) from being
implemented on U.S. submarines because of concems of the possibility of
sea water contacting the sodiwn coolant.
Uranium-aluminum alloy fuels clad in alum.inum have been used
extensively in research reactors. The uraniwn loading must be less than
35wt% uranium in the fuel material. Above this 35wt% limit it is extremely
d.ifficult to maintain the specitied homogeneity of the uratum throughout
the fu.el material that is required to prevent hot spots.[15] With the densities
of metallic uranium and aluminum taken as 18.8g!cm3 and 2.7g/cm3
respectively the following equation [12.],
Mu Pu___
--=--=--__..;....
Vmeat I+~( 100 -l)
PAI wt%U (2.1)
40
2.1.2.3 Unmium Alnmlnlde A111minum Dilpendon Fuel (UAla AI)
Dispersion type fuels are two phase alloys consisting of a fi asile isotope
bearing material that is uniformly dispersed in e matrix of nonfissile
material or diluent. These fuela are usually prepared by powder
metallurgy, a process in which fine powders of the fissile phase and
nonfissile phase are mixed, compacted, sintered, and rolled to form a
continuou& fuel material. The diapersion tecbtque offers the following
advantages when the diluent predom.inates in volume.
2) The potential for reaction between the fuel and the coolant is
essentially eliminated in the event of cladding rupture. Only
parti eles on the surface of the fuel material can be exposed to the
coolant.[17]
3) The path for heat flow from the fissile particles is through a highly
conducting metallic nonfissile medium which lowers the required
operating fuel temperatura.
41
relatively low temperature. Since alnminum metal melts at 660C, a
temperatura wbich can easily be exceeded during transient or accident
conditiona, it should not be used u a fuel matris or cladding material for
PWR operating eonditions.
Uraniu:m alnminide ~ aluminum dispersion type fuel is used in the
Advanced Test Reactor operated by the Idaho National Engineering
Laboratory with an average uranium loading in the fuel plates of 42wt%
uranium or about 60wt% UAI. As calculated from Equation 1.2, thi~;
Another more prom.ising fuel type is uranium silicide which has been
used to form a disparsion with aluminum. The uranium silicide
compounds of interest are UaSi which has a uranium density of 14.91g/cm3
and UaSi2 which has a uraniu.m. density of 11.3g/cm3. UaSi 2 has a
moderately high melting point of l665C while U3Si has a nielting point of
930C. U ,Si2 was shown to more stable under irradiation than U aSi.[ 17]
Uranium silicide- aluminum dispersion type fuels (U 3Sis- Al) offer
higher uranium. loadings than the UAlx- AI dispersion type fuels. Fuel
elements containing UsSix- AI dispersion type fuel of up to 45 volume
percent (45Vol%) UsSix, corresponds to a uranium loading of 4.75g/cm3,
have been succe&sfully irradiated in the Oak Ridge Research Reactor (ORR)
with maximum fuel temperatures of approximately 130C.[ 17] Also, it has
42
been reported that U3Si:.:- AI disperaion type fuela with a uranium loading
of 6glcm3 have been irradisted to a bumup of 50at'll.[21] However, this was
done with fuel maximum. operating temperaturf!ls at about low
temperature. At the operating temperatures of 500C or greater required
for a power producing rsactor, uranium sUicide fuels exhibit excessive
swelling under irradiation. Furthermore, uranium silcide fuel undergoes
rapid and gN&B awelling at fuel temperaturea in exceBS of 900C. Such fuel
temperatures can be reached quickly during a LOCA.{18] Thus, urarJum
silicide diaperaion type fuels are also not suitable for use in the power
producing reactors needed by SSNs.
development testa for UsOs- AI dispersion type fuel, samples were madep
and irradiated, evaluated, and deemed satisfactory up to a maximum
loading of 42wt% uranium (50wt% UaOs) in the fuel material. [12] With the
densities of the UaOa compound and aluminum taken as 8.4g/cm3 and
2.7glcm3 respectively, Equation 1.2,
Mue _ Pu,oe
Vmeat - I + PuA ( 100 _1)
PAI wt%Us0s (2.2)
43
yields a UsOs compound loading of 2.04g/cm3 for 50wt% UaOa. Since the
uranium maas fraction in U 30a is 84.5% as listed in Table 2.1, the uranium
loading is 1.73glcm3. lt has been estimated, however, that U 3 0a- AI
dispersion type fuels with a uranium loading of2.8 to 3.7g/cm3 could be
fabricated.[12] Based on atomic geometry considerations, a uranium
loading ofabout 3.6 -3.7glcm3 (about 80wt% UsOs) ia thought to be the
theoretical limit at wbich the continuous aluminum phase can be
maintained. This is required in order to facilitate beat removal from the
fuel element through the highly conducting continuous aluminum
matrix.[12) Higher uraniwn loadings than those mentioned above are
required for SSN reactor fuel elements.
A major drawback to the use ofUaOa fuel is that it reverta to U02 at
44
2.1.2.8 Unmlum Carbide aod Uranium Nitride Fu.el.u
45
lt should be noted that these fuela are beat auited for the liquid sodium
cooled reactor deacribed in Section 2.1.2.2. where ezcessive swelling can be
accommodated and the fuellwater reaction ia eliminated.
46
inner aurface of the cladding which will cause some awelling. Rod type
fuel elementa uaed in commercial reactors are comtructed with a plenu.m
at the top of each fuel rod where released fisaion guaes collect. In these
fuel roda, there is no fuellcladding bond, thus allowing fission gasses to
reach this plenum via tbe gap. Figure 2.1 sbowa the percentage of fission
gases released as a function of temperature. Although uo2 exhibits some
fission gas swelling it ia considerad to be one of the most stable under
irradiation and fission gas swelling reaistant fuels available.
Despite these limitations caused by poor thermal conductivity and
fission gas swelling, uo2 is considered to be the .fuel best suited for use in
the SSN PWR reactor design ofthis study. Furthermoret much operating
experience has been gained through the years with uo2 fuel clad in
zircaloy by itB use in commercial PWRs and to a lesser extent in research
rea~tors.
47
1000
100
~
~
Ji 10 ,/
~ ..... /
'~
~
J
1
/
.1
/
.01
900 1100 1300 1500 1700 1900 2100 2300 2500
48
the case of weak or defective cladding, fission gas pressure can result in
failure of the cladding.
3) High me~ting point: Almost ali materiais that have been used as
nuclear fuel cladding materiais have a lower melting point than
U02 (2800C). During normal operation, the average
49
temperature of the fuel in a power producing PWR is about
l000C and the average temperature of the cladding ia about
380C. lf a loss-of-Oow-accident were to occur, in a brief time
period, the temperature profile through the fueVcladding system
would Oatten which can posaibly result in melting of the
cladding. Thus a cladding material with a high melting point
increases the safety margin for the reactor.
so
where they may induce stre88 corroaion cracking or other
d.egrading phenomena. Also, in PWRa, uceseive hydrogen
concentrations in the coolant water can react with some potential
cladding materiais to form hydrides. Hydrides are very brittle
materiais which can result in cladding failure if formed in
high atresses regiona.
Zr + 2H2 -+ Zr02 + 4H
51
Table JJL Pouible cladding materiais.
Thermal Thermal
'l'bermal Mic:Toacopic Macroacc;pic
Atomie Denlity Coa.cluct- Meltina lt.bsorption lt.bsorption
Material Wei1ht {alem a) ivity Point (OC) Crou-Section, Cro-Section,
(W/m-K) :ta(cm -1)
<& <harn)
52
neutron economy ia necessary.[16]
Although una11oyed zirconium (zireoniwn metal) haa a lower
I.C9.8cJnl) than zircaloy {10.7cm-1), it ia not suitable as a cladd.ing material
S3
TabiE z.c. Zircaloy alloy series.
7..b:alo7-1 2.5
54
C- axis. Such complicationa can be overcome with proper fahrication
techniques anel orientati.on of the hexagonal crystal otructure.[22]
55
ga.dolinium. Witb proper design and distribution of Gd2s throughout the
reactor core, flatter power distributiona and low neutron leakage can be
achieved. A flatter power distribution resulta in a reduction of the reactor
power pealring factor which alao resulta in better fuel utilization.
Additional advantages to the uae of Gd20s u a solid aolution with U02 are
no displacement of water and little displacement of the fuel.
There are two potential diaadvantages to the use of Gd20s. Although
Gd:zOa ia physically compatible with uo2, the thermal conductivity and the
melting point ofthe fuel material islowered with its addition to uo2.[19]
However, for the reactor designa and fuel elements considered for this
study, this is nota problem. It was stated earlier that maximum uranium
fuel temperature heat would be encountered in the uo2 fuel elements
considered for this study ia 975C and that the melting point ofU0 2 is
2875C. Thus there is a wide ma.rgin to accommodate these undesirable
effects and gadolinium has been chose for this study.
It should be noted tbat for the 20% and 97.3% enriched reactor designa,
Gd20s is lumped into separate plates for reasooo that will be discussed in
detail in Chapter 5. In the 7% enriched reactor design, the Gd20a is
uniformly distributed throughout the reactoi" fuel elements.
56
Table 2JL &actmty control materiais.
Tbermal
.
Macroaeopic
Compound Cont.rolliDg Ahaorption
Element Croaa-Section,
I.a (cm1 )
s.c B 759
HfC Hf 102
,,_
&.zOa B 759
Gd203 Gd 49(XX)
E~0 3 Eu 4.8X)
lltOz Hf lW
HaBOs B 7tiJ
- Er 0
2 3 Er 162
Ag 63.6
Ag-In-Cd In 193.5
Cd 2450
51
Table 2.8. Iaotopea of gadoUnium.
Thermal
llotopic Microacopic
GadoliDium Atomic Abaorption
I aotope Abundance Weight
(alo) Croea-Section.
(q.) barns
1M 2.18 153.921 8)
Gadolinium
mass fraction 86.8%
.
Thermal
Macroscopic
Absorption 4900)
Cross-Section,
l:a (cm~l)
58
A. statecl in Chapter 1, H~ ia tbe coolant material by choice of the SSN
reactor type, the PWR. Water serves two functiona in this rea~Mr. It acts
aa a reactor coolant and aa a neutron moderator which elows down
neutrons to thermal energiea (..0.026eV) at which moet fiesion occur. Each
fi88ion releases an aversge of 2.4 neutrons with an average energy of about
2MeV.
With regard to reactor operation and contml, water haa two opposing
effects. lta neutron moderating characteristics contribute positive
reactivity to the reactor, while its neutron abeorpti.on characteristic~
From the discussion of this chapter, our SSN reactors will consist of an
arra.ngement of uo2 fuel at some enrichment levelo zircaloy - 4 cladding
and structural material, Gd20s burnable poison material and H20 coolant.
The remainder of this study will consist of determining the quantity,
distribution and arrangement of these materiais that will result in the
optimum utilization of 7%, 20% and 97.3% enriched uranium.
59
Table 2.8. lmportant physics properties of H:z().
c p(305CXJikJ.K) 5.7
kw (305C)(W/m.K 0.56
J1 w (305CXJ!Pa.s) 92x 10-6
60
CBAPJERS
Fuel tlement Deaip
61
design geometry is determined primarily by physica considerations since
heat removei is not the major concem. In conti.Duous operation high
power ructon, especially those that muat operate at high temperatures,
fuel element design geometry ie determined primarily by heat removal or
thermal hydraulica conaiderationa. Since the reactor designa considered
for this study are high power density, relatively high temperature pcwer
produciog reactors, fuel elem.ent designa witb a high surface to fuel volume
ratio shouid be employed. Of the two baaic power reactor fuel element types,
those uaing clad fuel roda and clad fuel plates, plates o:ffer the highest
surface to volume ratio. Thus plate type fuel elements have been selected
for this study.
The structure ofthe fuel platc (i.e., cladding and fuel material) has a
direct influence on the ability of the reactor core in question to obtain high
fuel burnup and thus a long l'tifueling lifeti.me. For the fuel plates
considoered for this study, the volume of the fuel plates, exduding that of the
cladding, is not completely occupied by fuel material. The remaining
volume is occupied by plate structural material, which is ued to form
structurea that are more resistant to fission gas swelling with respect to
fuel platea occupied by fuel material only. For the LEU case, a fuel
structure known as caramel type fuel haa been employed. For the HEU
reactor cores considered for this study, a lower fuel volume fraction ia
required in the fuel plates than for the fuel plateo of the LEU fueled reactor
cores. Thia lower fuel volume fraction enablos the use of a structure known
62
as a c:ermet that ia highly reaistant to fiaaion pa awelling enabling high
fuel bumup.
In recent y~, the French have utilized 7'*' enriched uo2 caramel type
fuel in the Osiria reactor which islocated at the Saclay Nuclear Research
Center in France. A description of theae fuel platea and fuel element has
been published by the French as a part of the atudies for conversion of
research reactor fuels from HEU to LEU.[12] It should be noted that fuel
plates similar to the French caramel fuel plates have been used in the
Shippingport reactor core 11.[ 18]
The caramel fuel plate used in the Osiris reactor takes the form of two
thin sheeta of zircaloy cladding enclosing a regular array of rectangular
uo2 platelets or caramels which are separated by small pieces of zircaloy'
Figure 3.1.[ 12] Thia type of design allows a uo2 fuel bumup of
approximately 60,000MWdll'.[13] Zircaloy separators which are each
bonded to tbe inner surfaces of both zircaloy cladding plates provide an
added restraining effect against fission gas swelling. Regular research
reactor fuel plates are composed
63
1.45.1_ _L
IL 2.22
T l-l1.s.&-J T
Top View
o.76ti IrJ
17.So&
1111 L
..
......_
Patelet
(C arame))
1.~
ZrSeparatora
T
14 -- Side Plate
64
Table 8.1 Feaaible dimenaions ofvarioua parta of
the caramel fuel plate.[12]
The caramel fuel plate ia well suited for the direct integration of the
bumable poison gadolinium oxide with the uo2 fuel platelets.
Experimental irradiation of caramel type fuel plates containing mixed
Gd20a-U02 onde haa already shown satisfactory bebavior.[12]
It was stated. in section 3.1, that the caramel fuel design increased the
allowable fuel burnup by increaeing tbe ability of the cladding to resist
swelli'ng dueto internai fission gas pressure. The cermet fuel design
provides cladding restraint as well as providing the fuel with tremendous
structural strength, enabling the fuel element to resist fission gas swelling
to high fuel bumupe. Cenneta are dispersions of ceramic fuel particles
65
UD2 Particlel
"ii ..
~
... ...
.. i
,
mbedded in Zircaloy
l~Diameter
1.~
T
Top View
Side Plate
Clad
core. Thinner cermet type fuel plates were used to model two other reactor
cores as discuased in Section 3.2. Cermet type fuels are also highly
corrosion reaistant since in the event of cladding failure; only those
particlea near the inside surface of the cladding will be in contact with the
reactor coolant.
The most common e:umple of a cermet is uo2 dispersed in a stainless
steel matrix material. In the proceeding sectione, irradiation testa that
have been perform.ed on these cermets will be cited. However, stainless
steel is not an ideal matrix material, since it has a relatively high
macroscopic neutron absorpti.on cross-section (I,8 ) of 258cmt. The
relatively large volume fraction of the stainless steel resulta in large
parasitic neutron losees. The characteristics of the ideal cladding material
described in Section 2.2.1 also apply to tbe ideal matri.I material. As a
result, it was reasonably assumed that zircaloy-4, the material selected for
use as a cladding. could replace the volume occupied by the stainless steel
in the cited testa without reducing the attainable fuel burnup.[ 10] Since the
large volume of matrix or structural material present in cermet type fuels,
66
regardleae of the particular material, will always reault in parasitic
neutron louea, cermeta have been atudied primarily for military reactors
rather than Cor commercial type reactore uaing approximately 3% enriched
U02.[16] As atated earlier, moat military reactora have employed HEU.
Tbus neutron economy was not of concem as it ia in LEU commercial
reactors.
The attainable fuel burnup of a cermet fuel ia directly related to the
volume fraetion of structural material present in the fuel plate. As the
volume fraction of the atructural material is increased the attainable fuel
bumup also increasea. The following irradiation testa were used to obtain a
reaaonable estimate of attainable fuel bumup 88 a function of uo2 volume
fraction in the fuel. This partial estimate is illustrated in Figure 3.3.
67
100
90
80
\
~
70
\
I 80
\
\
-I
a.
::s
50
40 1\
; \
= 30
20 \
10 \
o
o 1 o 20 ao o so so 10 ao 9o 1oo
-
UO'l Volume Fraction in Cennet
68
As a cermet fuel element is irradiated, damage to the fuel structure is
caused by a combination of the static and dynamic effecta of the fission
products. At low fuel bumups the major damaging effect is due primarily
to the dynamic properties of the fission fragmente (i.e., fission product
recoil in the matrix). At high fuel bumups where higher concentrations of
fission products are approached the major damaging effect is due to the
static properties of the fission products (i.e., fission gas pressure).
In order to combat damage due t.he dynamic properties of fission
fragmenta, fuel particle diameter in a properly designed cermet should be
large compared to the range of the fission fragmenta. Thus fission
products released from the fuel during reactor operation are confined to
narrow regions or damage zones surrounding the fuel particles, while
most damage is concentrated in the fuel particles. Thus an undamaged
fission product free region of matrix metal exista around around each zone
of damage which surrounds each fuel particle. This objective cannot be
achieved in a homogeneous fissile metal or two ph.ase alloy systems where
both the fuel bearing compound and matrix may contain fissile atoms. For
a given volume fraction of fuel, the volume of damagcd matrix is
proportional to the surface area of the particles. Thus the fraction of the
matrix subject to recoil damage can be minimized by the use of smooth,
spherical particlea as large as can be tolerated. Most fuels designed to take
advantage of the cermet dispersion principie have particlea of a Ieast
1001Lm diameter.[20] Schematic cross sections of cermet dispersant
systems are shown in Figure 3.4. The dispersed particles are assumed to
be spheres in a cubically close-packed array. Two particle sizes are shown
with a spherical zone of damaged matrix metal surround.ing each particle.
Figure 3.4a illustrates a poorly designed cermet where damage zones
69
Partiele
..age Zone
.b
70
the fuel pvticles wbicb preuurizea the mat.rix ahell causing it to expand
as a tbick~walled veaael U.Dder preaaure. ThusD the matrix swelling that
can be allowed will determine the maximum fu.,l burnup. Swelling limits
are determined on the baaia of allowabl8 dimensional changea or a
maximum atrain baaed on reduced ductility limit of the neutron embrittled
matrix.[18] In effect, the matriz material acta u the atructural material in
the fuel element. The cermet of Fip:re 3.4b ia mcre resistant to ewelling
than the cermet of Figure 3.4a due to ita continuoWI web of undamaged
matrix material.
In order for the design principies deecriOOd above to be effective, the
particlea muat be uniform.ly diapersed throughout a m.atrix that
predominatea in volu.me.[20] lf the particlea are not unifonnly dispersed
some fiuion product damage zones will overlap thus weakening the
matrii. If the fuel material predomina te& in volume, it remains possible to
design a eermet aystem in which fission product damage :wnes do not
overlap. However, in this case the structural etrength of the matri:z:
materie.l is significantly reduced and the susceptibility to swelling
approachea that of a plate type fuel element utilizing a continuou.s sheet of
uo2 fuel.
Reacto&" cores fueled with 7%, 20% and 97.3% enrichcd uranium were
modeled using fuel element designa adopted from the original caramel fuel
element design of the Ooiris reactor. lt.R geometry ia similar to that of
current UAl MTR-type fuel elements ueed in some research reactors.
71
Figure 3.5 illuetratea the 17 plate caram.el fuel element used in the 7%
enriched core. Figure 3.6 showa how these fuel elements fit together as
building blocks to form a reactor core. As n the case of the Osiris reactor
and many other research reactors using plate type fuel, the intra-.element
spacing ia set at lmm.
In order to facilitate the reactor core modeling process the following
mod.ifications were made to the original caramel fuel element,
1) Fuel element end spacings were decreased in order that the intra-
element gap and the end-spacing of two acljacent fuel elementa
will equal the width of a water channel.
2) To allow for a square lattice pitch, the width of the fuel plates was
increased.
72
0.8151 3~_......I-
1""'1
I
2.221 I
T I
I
2.631
I I
T I
I
I
I
81.04
I
Fuel Plate
Water Chan ne~ ._ . I
I
J
-
I
Side Plate I
-
...
""
I
I
I
I
I
I
-
I I
,_
~----------81.04---------t
I I Fuel Element
I
Intra-Element Gap
I /
I
i
... L
,
, L
f
I .1 L
,
1.~
I
-;:::.:::: /
T I
lv
.I
_l I
I I
I
I 1
I I
I
73
1) In the first thin plate reactor core, the coolant channel thickness
(2.63mm) remained as it ia in thick plate fuel element design of
Figure 3.5, increasing the water/metal ratio.
The modifications that were applied to the thick plate fuel elements
described above were also applied to the thin plate fuel elements. Also, the
number of fuel plates in the thin plate fuel element designs were increased
in arder that the thin plate fuel element ]attice dimensions be dose to the
thick plate fuel element lattice dimensiona. Use of larger fuel elements
reduces the ratio of structural material (i.e., side platas) to fuel material in
the core and thus decreases parasitic neutron losses. Ali relevant
dimensions for the five reactor cores considered for this study are
sum.marized in Table 3.2.
As stated earlier, the design of a reactor fuel element ia a balance
between neutronics considerations and thennal hydraulic considerations,
where for the high power density, relatively high temperature reactor,
thermal-hydraulics considerations dominate. Figure 3. 7 illustrates the
design space in which neutronic and thermal hydraulics are compatible.
If the fuel plate thickness (i.e., thin plate thickness) ia assumed to be
constant, a water/metal ratio exceeding r mu resulta in a positive void
coefficient of reactivity or the overmoderation of the reactor. Also,
increasing the water/metal ratio also reduces the heat transfer area to the
74
E.uluded du. to
u bdin
limit mthe LEU
cue and too hilh
a value olk eft'in
theHEUcue
overmoderation oflattiae
rHUltinc in a pomtivw wid
c:oefticiet of reaetivity
kefT
(min)
rmin rmu
t-1--- Undermoderated-- - - Overmoderated----t
75
For tbe aecond tbin plate HEU reactor cue, plate and coolant channel
dimenaiona were dflC!'eased in similar proportiona resulting in a constant
water/m~tal ratio. Tbia, however, increaaea the bomogeneity of the reactor
core and reduce8 k..,. Tbia can be compensated for by increasing the uo2
volume fraction in the cermet fuel. A disadvantage to decreasing the
coolant ebannel thiekneBS, as stated earlier, is the increase in the wetted
perimeter which increasea required pumping power. Thin fuel platea
provide the advantage of increaaed heat tranafer area and thua lower fuel
centerline temperatures. However factors exiat which prohibit fuel plates
from being made extremely thin. Some of these are listed below
76
cover the metbods uaec:l to design and analye each reactor con considered
while Chapter & presente the resulta of the analysi1.
77
Tule 8.1. Fuel element ehanu:teristica.
FissU.E PABT
Fuel Material U02/Zircaloy-4 U02)Z!rcaloy-4 U02/Zircaloy-4
Enrichment 7%-97.3% 97.3% 97.3%
U02 denaity(glcm3) 10.3 10.3 10.3
Thickness(mm) 1.45 0.6 0.5
Active width(mm) 75.45 74.90 74.26
Platelet(caramelXmm) 17.34 N.A. N.A.
Spacing between plateleta(mm) 1.53 N.A. N.A.
SIDEPI,ATES
Material Zircaloy-4 Zircaloy-4 Zircaloy-4
Thickness(mm) 3.0 3.0 3.0
Width(mm) 81.04 80.90 80.26
FUEI. EI.EMEN'f
Nu.mber of plates per element 17 31 :J)
Cross-section(m.m) (81.04x81.04) (80.90x80.90) (80.26x80.26)
Lattice pi tch(mm) (82.04x82.04) (81.90x81.90) (81.26x.81.26)
78
In Chapter 1, certain operating characteristics and design
specificationa for a modem SSN reactor were selected as derived from the
performance requirementa of a modem SSN. Chapter 2 outlined the basis
for which the reactor fuel, cladding, coolant anel reactivity control material
(bumable poiaon) were aelected iD order to meet the required reactor
aperati.Dg characteriatica and deeip apeci6cationa. Chapter 3 descriood
the reactor fuel element designa chofien for this study, which are
conatructed baaed on the required reactor operating characteristics selected
in Chapter 1. This present chapter ia divided into two sections which cover
the reactor physica and the thermal hydraulic analysis methods used in
this atudy. However, as stated in Chapter 1, th.ermal-hydraulics
considerationa are assumed not to be limiting for the reactor designa
modeled in this study. Thus the design effort focwr;es on the reactor physics
{i.e., the a(ijustment of the reactor design to aatisfy ali relevant reactor
pbysica criteria). Following the reactor physics analysis, a simplified
thermal-hydraulic analyais ia however included to verify that fuel element
temperatures are within acceptable bounda and tbat the required coolant
flow ratee needed to remove hat are practical. All analytical methods
employed in thia study are covered in this chapter.
Table 4.1 aummarizes the reactor designa conaidered for this study.
Three reactor cores fueled with 7%, 20%, and 97.3% enriched urani um are
considered. For the HEU case (97.3%), two additional reactor core designa
are considered which use fuel oonta.ining thinner plates. AB stated in
Chapter 3, a thinner fuel plate reduces the required fuel center-line
79
Table 4..1. Reactor deaip.
operating temperature. For one thin plate design, the coolant channel
thickness is reduced in order to examine the eff'ect of water/metal ratio on
reactor physics and aafety parametera.
Table 4.2 aummarizes the de~ign specifications and operating limita
that have thus far been selected for each reactor core listed in Table 4.1.
80
Dadp Paramelar s,mbol ....
. data.
Table 4.1. Reactor detiJjp.
Coostraint
Buckling 82 Unknown -
Control Swing Akeff Unknown 1.04- 1.24
81
For the comparative purpoaes of tb.ia atudy, a aimplified one-
dimenaionalateacly-atate overall core reactor phyaica calculation ia used to
model the reactor corealisted in Table 4.1. With thia model, tb.e spatial
dependeoce of neutron fluz and fuel depletion (burnup) are neglected. (The
consumption of fuel ia treated as coDStant in alllocatioll.l of tbe reactor
core. In an actual reactor, the neutron fluz ia greateat in the center of the
core. Thua fuel depletion ia alao greateet in the center.) Tbia model also
does not eimulate the etrecta of control rod motion or atartup, shutdown and
transient behavior.
For the one-dimensional overall core model the entire reactor core is
characterized by each reactor physics parameter employed. For this
analysis, these parameters are,
82
4) Power denaity (q"'ave,r> wbere the aubecript (r) refere to the
retleeted nactor. A sublcript \..i) deaignatee an unreflected
reactor core. The specification of q"'ave,r seta the reactor core
volume (V) by tbe following equation,
... Q
q ave,rv
core (4.1)
With items 1 through 8, all important information about the steady state
operation of a nuclear reactor can be determined. A three-dimensional
steady state analysis can provide space dependent burnup data and hence,
a better estimate of the end-of-cycle core materiais inventory. It would also
83
provide a more accurate estimation of keft"= j(t) and Akeff. However, as
stated in Chapter 1, it was decided that such refinement is unnecessary for
the comparative purpoaes of this study.
Figure 4.1 illustrates the relationship and interdependence of each of
these parameters which together describe the operating reactor system. A
certain percentage of the composition of this system is fuel material and a
certain percentage is non fuel material. The fuel is consumed in a nuclear
reaction to produce power for an operating time, after whlch the fuel has
reached a burnup levei (i.e., a certain percentage of fuel has been
consumed). At any particular time during the operating time span the
system h,11S excess reactivity or excess capability trt sustain the power
producing reaction. This excess capahility changes over the operating
time. The range of excess reactivity over the operating time determines the
amount of control capability that must be provided to this system. Some of
this capability is supplied the bumable poison (Gd203), a non fuel material.
84
fhed ~
InPJatee
Vol%(U02 ~
Material a e ~
Vol%(GdtOs>
Vol%(Zr-4)
_L
Power
Q(MW) I
I
q-~[~~~~~
Operating
Time
trt (d)
lnpgt
--------------------~-- --~--------~------------ ----* - ----
Outwt
Amount
of Fuel
Consumed
System
Reactivity ..........~-----~ k(. /(t) ,___ __.... 2
t--------\ B
Control
Swing .
85
Design apace for reactor core of fixed
Uranium enriehment (e).
RefueliDg time (trf).
Total power
Akeff
(Cont1'0l Swing)
ketJ = f(t) BU
(System (Mechanical
Reactivity) Bumup)
In Plates
Vol%(U~)
Vol%<Gd.JlJ)
Vol%(Zr4)
86
In tbia fipre each ci.rc:le representa ali poaeible valuea of each variable
parameter. The deaip apace or repon of overlap of the circlea repr0aents
the accept.ble range of valuee of each variable parameter in combination
with the ra.np ol acceptable valueo of tbe other variable param.etera. Thus
each reactor cora muat be deaipecl in order tbat the value of each of these
parametera lie in the deaip apace. ODe can aee by inapection ofFigures 4.1
and 4.2 that tbe one-dimeuaional calculation uaed for tbia atudy requires
iteration in orcler to acijuat tbe reactor phyaica deaip parameters to lie in
the design space.
To perform tbeae iterativa 1-D calculations the EPRICell code ia
employed.(9] AB ahown in Fipre 4.1, tbe parameters above the horizontal
daahed 1ine are required aa input to EPRI-Cell while the parameters below
the dashed line are produced in the EPRI-Cell output. Tbus the valuea for
q"'ave,r \B2 and Vol%mCU02. Zr-4, Gd20a) are varied in the EPRI-Cell input
to cause the values of BU, kefr z f(t) and Akefr to satisfy the constraints listed
in Table 4.2. At thia point the value of q"'ave,r \B2, Vol%m(U02, Z'r-4,
Gd20s), BU, ketr and Akeft' will simultaneoualy lie in the design space of
Figure 4.2.
For each core deoign, Figure 4.3 illustrates the variable input design
parameten (physical reP~tor design acijustments) of q'"ave,r\B2 and
Vol%mCU02, Zr-4, Gd203) with regard to the complete core system. The
variable input design parameten (pbysical characteristics which are
variable) a.re contained in c:irclee while the physical characteristics which
are c,_ J&tant (pbysical characteristics which are not design variables) are
contained in rectangles. The physical basis for the variable input
111
parameters Q ave,r \B2 and Vol%mCU02, Zr_., Gd20a) for each reactor core
design is discuesed below.
87
CD.re (1)
For reactor core design 1 which utilizes 7% enriched caramel type fuel,
it is desirable for the uo2 volume percent in the fuel meat to be aslarge as
possible in order to maximize available reactivity. Thus for this core, the
UO?~Zr-4 volume percent ratio in the fuel meat ia fixed at what it is in the
original caramel fuel design. Note that the Zr-4 structural material in the
fuel meat ia structural material as described in Chapter 3. Also, for this
LEU design, the reactivity control material (Gd203) ia mixed directly with
the uo2 fuel material. Thus the variable input design parameters 88
These parameters are adjusted in the EPRI-Cell input to cause the values of
BU, keft' =f(t) and Akew to satsfy the constraints listed in Table 4.2.
88
Cores (2.3.4.5)
For reactor core designa 2,3,4 and 5, the U02 volume percent in the fuel
plate must be lower than that of eore 1 in order to reduce excess reactivity to
a controllable levei. Tbue for thie core, the UO:I{lr...f volume percent ratio
in tbe fuel meat ia a va.riable input deaign parameter. AB discusaed in
Chapter 3, a lumped gadolinia diatribution wu employed for these cores.
For theae cores the thickneu ofthe Gd2a plate lump was varied. Note that
as the lump thickneu decreaaea, the tbickne11 oC tbe cladding which
covera the lump muat increase proportionally. Tls ia discussed in detail
in Section 4.1.2.3. Thua the variable input dcsign parameters for these
cores, as illustrated by Figure 4.3b are,
These parameters are adjusted in the EPRI-Cell input to cause the values of
BU, ketr = j( t) and AkeK to satisfY the constraints liated in Table 4.2.
89
Reactor Core
...
q ave,r
~v
>'
~
core -""""ly B
2
N(U~)I
{N(Zr-4~ (NcZr-4~
N<Gd..A>
90
ReaetorCore
Fuel Platea
Fuel M0at ---
Clad
Channel Poison Platea
91
Sectiona 4.4.1.- 4.1.4. describe the methoda uaed to model the reactor cores
ofTable 4.1 using the EPRI-Cell code.
92
Control La.nguage (JCL) and accompanying EPRI-Cell input data. Job
Control La.nguage controla the data input proceaa to EPRI-Cell and the data
output proceaa from EPRI-Cell to appropriate memory locations and
retrieval quea. In order to further reduce computer usage costa, each batch
job waa aubmitted and nm during night and weekend hours and specified
as a low priority job. Low priority apecification, at times, :resulted in
signiticant time intervale between data aubmi88ion and output file
retrieval. Chargea per CPU hour were prohibitively high for full priority
batch joba regardless of the time period in which they were submitted.
As stated in Section 1.3, EPRI-Cell computes the space, energy, and
bumup dependence of the neutron spectrum in light water reactor fuel
cella. lta output consista mainly of broad group, macroscopic, exposure
deper,dent cross-sections for subsequent input into multidimensional
transport theory codes or diffusion theory codes such as DIF3D or REBUS-3
(this ia discussed further in Section 6.2). EPRI-Cell combines a GAM
resonance treatment in the fast and epithermal energy ranges with a
THERMOS, heterogeneous integral-transport treatment in the thermal
energy range. The original GAM and THERMOS codes have been modifi.ed
for use in EPRI-Cell; these modifications are fully described in the EPRI-
Cell users manual. The GAM and THERMOS cross-aectiori libraries
coru;ist of 68 and 35 energy groups respectively. These cross-section sets are
collapsed by EPRI-Cell into 1, 2, 3, 4 or 5 energy groups, according to the
specificati.on of the user. The broad-group energy break points used by
EPRI-Cell are listed in Table 4.3.
A modified version of CINDER, which is a general 'point' program that
evaluates the time dependent concentrations of coupled nuclides following
irradiation in a specified time-dependent flux, is incorporated into the
93
Table 4.3.. Energy break points.[9]
Numberof
Broad
Groups
Lower 5 4 3 2
Energy
ofGroup
1 0.821 MeV 0.821 MeV 5.53 keV 0.625 eV
EPRI-Cell package. The modificatim .... made to the CINDER program are
also fully described in the EPRI-Cell user manual, Reference [9]. Built into
CINDER, are depletion chains which are distinguished from fission chains
for the fission products. These chains include fuel and transuranic
isotopes as well as burnable poisons. The 21 depletion chains contain 116
linear nuclides: 27 distinct heavy elements and 19 bumable poisons. The 69
fission chains of CINDER cont.ain 367 linear nuclides with 179 distinct
fission products. The number of depletion calculations perfonned and
timesteps between each is specified by the user {See Appendix E).
Figure 4.4 illustrates the general flow of data during an EPRI-Cell
depletion run. The output of each iteration is processed into ECDATA files
with later entries overriding earlier values.
94
Input
"'IHERMOS"
Thermal Raqe
Calculation
"GAM"
FaatRanp
Caleulation
Generate Broad
Group Croaa-Sections
"ClNDER"
Space Dependent
Bumup
'ECDATA
Files
End
95
I
I
I
ReOected I
I
Reflected
C'l'e:C'r,)
fCD
c
~:tS
I
z
I
I
I
I I
D I A
1-t. Ce~
y
As illu.strated in Figure 4.5, plate type fuel elements are modeled by EPRI-
Cell as multi-zoned infinite slab unit cells. The one-dimensional slab
geometry unit cell cal~.llation is infinite in the Y and Z directions.
Conditions in the X direction are reflected infinitely at boundary planes
ABC and DEF which represent symmetry of the various zones of the
particular fuel element. Dueto symmetry, only the half thickness of the
particular zone in which the symmetry planes occur need be considered.
Each zone can be clivided into separate space intervals. These are the
smallest subdivisions of a eell andare chosen such that the flux is
deten:IV.ned at the midpoiut of the interval (the midpoint of the interval is
called a space point). EPRI-Cell has the capability to model40 zones and 60
space points.
96
Each zone in the fuel cell can represent fuel, cladding, coolant
channela, burnable poiaon of any other materi&l component o( the fuel
e1ement in queation. EPRI-Cell breab each zone into compositiona and
requirea input specifying the volume percent of each material composition
in each zone and the number .denaity of each nuclide in each composition.
EPRI-Cell haa the capability to treat 20 compositiona and 36 nuclides.
The EPRI-Cell code was used to mock up the reactor cores of this study
with one-dimenaional calculationa. In general, une-dimensional
calculations performed on high power denaity reactor cores are used only
for preliminary or survey type analysis.[12] Since the objectives of these
calculations are only to provide an estimate of reactor core aize, refueling
lifetime, reactivity coefficients, and plutoniwn buildup for comparativa
purpoaes, on~dimensional calculations were deemed appropriate. Other
reactor design considerations such as spatially dependant burnup, control
element motion and atartup, shutdown and transient behavior have been
neglected for the comparativa purposes of this study. Possibilities for
further, more detailed analysis are discussed in Chapter 6.
This section describes the methods used to model the reactor cores
considered for this study which are summ.arized in Table 4.1. Also
described in this section are the methods used to calculate the values of the
particular EPRI-Cell input parameters listed in Table 4.4 which represent
the reactor core design variables described in Figures 4.1 and 1.2. Each
calculation is baserl on the fixed and variable input data listed in Table 4.2
97
Table 4.4. EPRI-CeU input variahles uaed for reactor design.
and also the fuel element design dimensione of Table 3.2 and materiais data
presented in Chapter 2.
Ali EPRI-Cell input parameters not used as reactor design variables
are ruscussed in detail in Appendix E whlch provides the following
information,
98
4) The first and second depletion timesteps of the reactor core 3
EPRICflll output file.
Core (1)
As discussed earlier, for this core which is fueled with 7% enriched
99
00
I
I FueJ I
r~~~~
00
100
Cores (2.3.4.5.)
For reactor core designa 2,3,4 and 5, a lumped gadolinia distribution
was employed in order to take advantage of self ahielding effects in the
gadolinia. As will be discussed further in Chapter 5, this preventa the
rapid depletion of gadolinia near B.O.C., thus providing reactivity control
towards E.O.C. Unlumped gadolinia depletes faster than the uranium fuel
since it has a larger absorption cross-section. For these designa, the
gadolinia waslumped into fuel plate locations and clad with Zr-4. This
requires an expanded fuel cell model.
Calculations were performed with burnabl~ poison plates occurring at
every fourth and sixth plate location as illustrated by Figures 4.7a and 4.7b.
As will he discussed in Chapter 5, the reactor core with burnable poison
plates distribut.ed every sixth plate exhibited a lower control swing, Akeff
For these designa, the fuel element is modeled with four zone types, fuel,
cladding, coolant and burnable poison zones. The planes of symmetry for
this fuel cell occur in the center of the bumable poison zones and the center
of the middle fuel plate or zone with respect to the bumable poison zones.
However, the fuel cells shown in Figures 4.7a and 4.7b contain three planes
of sym.metry and not two as in the case of Figure 4.6. This was done in
order to verify, using t.he corresponding EPRI-Cell output, that the code was
performing a symmetric depletion calculation about the center planes of
symmetry. In other words, to verify the reflection of boundary conditions
across the symmetry planes.
In this case, the fuel zone consista of the compositions, uo2 and
zircaloy-4 structural material. The U02 consista of the nuclides U235, U238
andO. No Gd20a is present since it is lumped into a solid sheets occupying
fuel plate locations. The zircaloy-4 in the fuel and cladding zones is treated
101
Reflected
oo"C cond:ition.1
..,.,.-.__ boundary__.. O<;
condition1
adolinia Lump
Piate
Refled:ed lad
boundary
~eondition 1 00
co 00
~
....-i
102
as in the above case (core 1). Also, the water zone is treated as in the above
case. The bumable poison zone consista of the composition Gd203 which in
turn consista of the nuclides Qd157, Qd155 andO. The remaining
gadolinium isotopes are treated as in the above case.
It must be noted that for EPRI-Cell calculation involving a change in
the fuel zone or plate thickness, the input parameters Res(2, J) and and
Res(3, J) must be recalculated. These parameters are described in
Append.ix E.
reactor fuel elements considered here, the reactivity effects of the zircaloy-4
side plates and a portion of the intra-element gap water mUBt be taken into
account. Together, the side plates and the intra element gap comprise
8.53%, 8.55%, and 8.61% ofthe total core volume for the thick plate/thlck
channel, thin plate/thick channel and thin platelthin channel reactor
designa respectively. To model the extra zircaloy-4 of the side plates, the
total cross-sectional area of the side plates of each fuel element design was
divided by the total wetted perimeter of the fuel plates in a fuel element and
added to the actual cladding zone thick.ness. This effective cladding zone
thickness (effective thickness with regard to neutronics considerations) is
used in the EPRI-Cell input. The modified cladd.ing zone thickness ia given
~y'
103
where,
(4.3)
104
I I Fuel Element
I I
lntra-Element Gap
l I L
I I _,
I 1 ~ L
I
I I I
I I I
Region of
I
L
I , Intra-Eiement
1.21_ I
Gap Treated as
T _I
I
I
I
Extra Water
I ! ,-
,
I I -
I I
I I
I
I I
---1~
Figure 4.8. Fuel element extra water.
where
SJ = Lattice pitch
tg = Intra-element water gap thickness
tw = Actual water channel thickness
t'w = Modified water channel zone thickness
105
According to the earlier discussion, the thickness of the gadolinia
lu.mps is a variable input design parameter for the cores utilizing 20% and
97.3% enriched uraniu.m, Vol%{Gd20a) in the fuel plate locations. This
Cores (2.3.4.5)
For reactor core designa 2,3,4 and 5 which employ a lumped gadolinia
distribution, the lu.mp thickness was used as a design variable (i.e., the
lump thickness was varied for the iterative design calculations).
Throughout theae calculations, the su.m thickness of the Gd203 lu.mp and
associated cladding must be equal to the regular fuel plate thickness. For
each lump thckness variation, the corresponding cladd.ing thickness can
be calculated by the following relation,
(4.4)
where,
106
4.1.2.4 Com.posltion Volume PerceiUB In tbe Fuel Meat
For each reactor core design, the volume fraction (volume percent
divided by 100) ofthe uo2 fuel and the Zr-4 structural material in the fuel
meat must be determined and input into EPRI-Cell. As discussed earlier,
the the volume percent ratio of uo2 to Zr -4 structural material in the fuel
meat ia a design variable for reactor cores 2,3,4 and 5 which utilize the
lumped Gd203 distribution. For reactor core 1, this ratio is fixed. The
volume fraction of each composition is specified in the EPRI-Cell input file
by the parameter VOLFRC(K,L), where K refere to the particular material
composition and L specifies the particular zone. Note that for any changes
ofthe number densities ofthe nuclides Tfl35 and U238 or volwne percent
U02 which bears these nuclides, the values of the resonance input
parameters Res (4, tJ235) and Re~ (4, tJ238), (Res (5, U235), Res (5, U238) must
be recalculated. This is discussed in detail in Appendix E.
Core< I>
For reactor core design 1 which utilizes 7% enriched caramel type fuel,
it is desirable for the uo2 volume fraction in the fuel meat to be as large as
possible in order to maximize available reactivity. Thus forthis core, the
Vol%m(U02) in the fuel meat is nota design variable. In thls case the U02
ia actually a mixture of uo2 and Gd20a. The following equation is used to
calculate the U02 volume fraction, Volm(U02), in the fuel meat of the
original caramel fuel plate design.
(4.5)
107
where,
The fixed uo2 volume percent in the fuel meat of the original caramel fuel
plate Vol%m(U02) is calculated to be 84.44%.
The corresponding fixed Zr-4 volume percent, Volm(Zr-4), in the fuel
meat is determined by the volume fraction relation,
(4.6)
Core(2)
As calculated above the m.a:ximum uo2 volume percent allowed for this
study is 84.44% (Vol x 100), that of the original caramel fuel plate design.
Since a uranium enrichment of 20% is used in this core and as will be
shown in Chapter 5, the U02 volume percent Vol%m(U02) in the fuel meat
must be decreased in order to reduce the core excess reactivity to a
controllable levei. Th118, as discussed earlier, the uo2 volume percent in
the fuel meat is a design variable. Since t.he optimum Vol%m(U02) for this
design lies in the range,
108
a caramel fuel design was employed. As discussed in Chapter 3, fuel plates
with fuel zone uo2 volume per~nts lesa than 50% will employ cermet fuel
plate design. With each variation the corresponding Zr-4 volume percent in
the fuel meat was calculated by equation 4.6. (The calculated fuel meat
Vol%mU02 for each core design islisted in Table 5.1).
A reduction in the Vol%m(U02) requires a reduction in the fuei platelet
(4.7)
V= 4~
{Rcs + l)wp (4.8)
where Vis the U02 volume fraction, Volm(U02). Rearranging Equation 4.8
yields,
(4.9)
Solving the above equation by the quadratic formula and rearranging yields
(4.10)
109
Thus, solving Equation 4. 7 for w 1 ,
(4.11)
(4.12)
(4.13)
The value ofw8 can be found by substituting the value ofwc into the
constraint equation, Equation 4.11.
Cores (3.4.5)
For reactor core designa 3,4,and 5 which are fueled with 97.3% enriched
uranium (i.e., HEU), a low fuel meat U02 volume percent is required to
maintain controllable excess reactivity. Since the U02 volume percents for
these cores are lesa than 50% (this was initially assumed and later found to
be true) a cennet fuel design is employed. The uo2 volume fraction was
varied over the interval,
110
where 20% is the lower bound of the cermet uo2 volume percent, below
which irradiation behavior can not be estimated (see Figure 3.1 ). The
corresponding Zr-4 volume percents are determined by the volume fraction
relation,
(4.6)
Core (1)
As shown in Figure 4.3a, for reactor core design 1 the Vol%m(U02-
Gd203 mixture)Nol%m(Zr-4 structural material) r a tio in the fuel meat is
constanc.. However, the fuel material consists of a mixture of U02 and
Gd20a where the UOvGd20a ratio is a design variable. Thus with each
variation of the wt%Gd203 in this mixture, the nuclide number densities in
the fuel/bumable poison mixture (U02-Gd20a mixture) must be
111
recalculated. In effect, the U02-Gd20a mixture is treated as a single
material composition in this case. The nuclide number densitiea in the
Zr-4 structural material volume as well as in the cladding and coolant
zones are constant.
Cores <2.3.4.5)
As shown in Figure 4.3b, reactor core designa 2,3,4 and 5, which utilize
a lumped burnable poison distribution, the Vol%m(U02Wol%m(Zr-4
structural material) ratio in the fuel meat is a design variable. The fuel
consista of pure uo2 while the bumable poison lumps consist of pure
Gd203. Thus the nuclide number densities in the U02 fuel volume Zr-4
structural material volume, bumable poison lumps ar.. d cladding and
coolant zones are constant.
The equations used to calculate the nuclide number densities for each
material composition are described below for each composition. Also, the
parameters used in each of these equations are defined as,
.....
uoa. Gib.Oa
For tha U02 fuel of7%, 20% and 97.3% enrichment wlch consista of a
mixture of 1J235 and U238 atoms, the average molecular weight of the
uranium atoms is given by the relation,
1 _ [ (1- e) + e ]
Mave- M(U238) M(U 235) (4.14)
The weigbt percent uranium in the uo2 compound is then given by,
f=- Mave
Mave + 2M(O) (4.15)
The number density of the nuclides {]235 and {]238 can then be determined
by the following equations,
(4.16)
The term (1- w) is the weight percent ofU02 in the U02-Gd203 mixture and
(0 is thc weigbt percent of uraniun:. in the U02 compound. For reactor
cores 2,3,4 and 5 which do not utilize the lumped bumable poison (Gd203)
distribution, (w) is set equal to -zero.
113
The number density of the Gd20a molecule ia given by,
(4.18)
where M(Gd203) is the molecular weight of the Gd20a molecule (See Table
2.7). The number densities ofthe nuclides Gdl55 and Gd157 are the given by,
(4.19)
(4.20)
where a/o(Gd155) and a/o(Gd157) are the natural atomic abundances of the
respective nuclides (See Table 2.6). Note that the other gadolinium isotopes,
Gd154, Gd156, Gd158 and Gd160 must be treated as void. Upon specification of
the isotope Gd155, EPRI-Cell automatically initializes Gdl54, Gd156 and Gd158
in the naturally occurring proportions. This is discussed in
Appendix E.
For the oxygen number density can now be determined by,
where the first and second terma on the 1ighthand-side are the
contributions from the U02 and Gd20a compositions respectively. The term
(1- w) is t.he weight percent U02 in the U02-Gd203 mixture and the term
114
( 1 - 0 is the weight percent oxygen in the U02 compound. For reactor co:-es
2,3,4 and 5 which do not utilize the lumped burnable poison (Gd203)
distribution, (w) is set equal to zero. For tha second term on the right-hand-
side, the coefficient rt!sulta since 1.5 oxygen atoms ar e present for every
N(Zr-4) = p(Zr4XN_A)_---:-
M(Zr-4( 1024barns/cm2) (4.22)
where the asso<:iated Zr-4 properties are listed in Table 2.3, Thus N(Zr-4) is
calculated to be 0.042518atomslb-cm.
H20 Coolanl-
'rhe number density of the H20 molecule is given by,
(4.23)
where the associeted H20 properties are listed in Table 2.8. Thus N(H20) is
calculated to be 0.02429atoms/b-cm. The number densities of the hydrogen
and oxygen constituents are given by,
115
(4.24)
(4.25)
For ali the calculational results given in this thesis, primarily Chapter 5,
the value of Proom temp<H20) =l.Oglcm3 was used A correction to P305C
(i.e.,lower H20 density in core) is discussed in Section 5.8. Thus N(H) and
N(O) are 0.04840atoms/b-cm and 0.02420atoms/b-cm respectively, where
P305oc(H20) = 0.74glcm3.
As listed in Table 4.2 and discussed in Section 1.1, the total desired
reactor core power, Q, is 50MW, on which ali reactor core calculations are
based. The reactor core power is specified by the EPRI-Cell input
parameter POWR (Watts/cm of height). The value of POWR is given by the
relation,
where q"'ave,r ia the reactor core average power density. The cell
thickness,tcelh is detennined by summing the thicknesses of the individual
fuel cell zones used to represent the fuel element of the particular reactor
core under consideration. The unit thickness,tunit, is equal to lcm and
conserves dimensione. The reactor core average power density q"'ave,r is
given by the Equation 4.1,
116
q '" ave,r =V Q
e ore (4.1)
where Vcoreis the reactor core volume. Since Vcore ia not known initially,
q"'ave,r can not be calculated and therefore must be guessed and is
...
q max =
nr q ...ave,r s 11oookwiLI
lOOkWIL (4.27b)
where q'" mu: ia the maximum core power density and !lr. which is defined
below from Equation 1.2, is the power peaking factor for a finite cylindrical
reflected reactor.
ar -_q"' max
111
q ave,r (4.28)
111
n _2,q max
r - 3 "'
q avc,u (4.29)
117
I I I I
Retl~ 'Reflectori
:..c < Core ------:i~>-..,.:.< >
FutOux, t Thermal
'
I
I
I
I
1 'lllermal ftux
: unreflec:t:ed ____,~~""'"
: baro reador,
2
o Rc Rr
Distance from center of reactor core
118
The volume in cm3 for tb.e reflected reactnr core for a particular total
power Q (SOMW) is given by rearranging Equation 4.1.
v - I Q Y 1 MWV__l__t_)
core,r- \q 11 'ave,r~1()(X) kW ~l(XX) cm3 (4.31)
H=2.5
R (4.32)
as in the case of the reactor which J)CJwers the USS Savannah. The olume
of a cylinder is given by,
for the reflected reactor cores of this study. Solving for Rr gives,
Rr =~{V-;
'Vi:Si (4.35)
Hr =2.5Rr (4.36)
119
For a reactor core of finite dimensione, some neutrons are lost to
leakage. The term used to account for this loss for a bare unreflected
reactor core modeled in 1-D is known as the geometric buckling, B2 , which
is a function of reactor geometry. The value of this term affects the value of
keff The geometric buckling, B2, for an unreflected finite cylindrical
reactor is given by,
(4.37)
where Ru and Hu are the effective height and radius of the unreflected finite
cylindrical reactor and taken for this approximation to be equal to the
actual unreflected height and r8d.ius. For a constant total reactor power,
Q, Ru and Hu are larger than Rr and H r. Thus, if the values for Rr and H r,
as derived from the guess of q'"sve,r are used in Equaton 4.37, the neutron
leakage loss 88 represented by B2, will be overestimated. Since the reactor
cores considered for this study are reflected (i.e., surrounded by a water
shroud), neutron leakage is reduced, q"' ave is increased and the required
reactor volume to produce a total power of 50MW decreases. Thus for the
approximate comparative purposes of this study, it is 8ssumed that the
tenn B2, 88 calculated for the unreflected finite cylindrical reactor also
operating at a total power of 50MW, is representa tive of the neutron leakage
of the 50MW reflected reactor. Both reflected and unreflected reactors have
a height to radius ratio of 2.5. The volume of this unreflected counterpart is
determined by substituting q"' 8 ve,u as defined by Equation 4.30 into
Equation 4.31. Thus,
120
V eore,u = (a .~ ) Jn ~:l~~ ~)
q ave,r 1 em
3 (4.38)
(4.40)
Back substituting the value ofRu into Equation 4.36 for the unreflected
reactor gives,
Hu=2.5Ru (4.41)
Substituting the values of Ru and Hu into Equation 4.37 yields B2 for the
121
discusaes a more accurate method to calculate the constant value of
reflector savings or extrapolation length.
Core <1>
Figure 4.10 is a flow chart of the design procedure used to model reactor
core 1. In order to model the fuel cell geometry, zone thicknesses are
calculated according to Section 4.1.2.1 and 4.1.2.2. The material volume
percents are calculated as discussed in Section 4.1.2.4. A value of the
weight percent Gd20a wt%<Gd20a) present in the U02-Gd20a mixture is
guessed which typically ranges from 1-10%. With this value, the nuclide
number deitBities within this mixture are calculated by the methods
described in Section 4.1.2.5. As discussed in Section 4.1.2.6, a value for the
average power density (q'"ave r> is g"..lessed, which also sets the core volume
'
and dimensione by which the value ofthe neutron leakage term, B2, is
determined. This datais ent.ered into an EPRI-Cell input file as outlined in
Section E.2 of Appendix E, and used to run EPRI-Cell. The values of keff for
each timestep, k = j(t), and the value for burnup, BU, are obtained from the
output file. H these values do not satisfy the constraints of Table 4.2, the
values for wt%(Gd20a) snd q'"ave r are adjusted in further EPRI-Cell runs
'
122
to yield k = /(t) and BU which satisfy these constraints. At this point, ali
reactor deaign parameten willlie in the design space of Figure 4.2.
Core (2.3.4.5)
Figure 4.11 illustrates the design procedure used to model reactor cores
2,3,4 and 5. Ali material number densities are calculated according to
Section 4.1.2.4. The fuel cells are modeled as discussed in Section 4.1.2.1
and 4.1.2.2. A velue for the thickneu ofthe burnable poison (Gd203) lump
is guessed, and the corresponding poison plate cladding thickness is
calculated as discussed in Section 4.1.2.3. The U02 and Zr-4 volume
percents in the fuel meat, Vol%m(U02, Zr-4), are guessed based on the
discussion of Section 4.1.2.5. AB described in Section 4.1.2.6. a. value for
q"' ave,r is guessed, which seta the v alue of Vcore by which the neutron
123
Start
Guess wt%<GdA)
,..
""" present in the uo2- Gd.A
fuel mixture
til
Guess q ave,r ;.... vcore ,...B2
Run EPRI-Cell
(Depletion calculation)
Innut
-------------------------- -------------------
Retrieve output file
No keff =j(t)
Satisfies constraints of Table 4.2
Yes
No BU
Satisfies constraints of Table 4.2
Yes
Finish
124
Start
111
Guess q ave,r ,.,. vcore ~B2
Run EPRI-Cell
(Depletion calculation)
Iu.uut
t-----------~------* ------------- Oumt
Retrieve output file
No keff = j(t)
Satisfies constraints ofTable 4.2
Yes
No BU
Satisfies constraints of Figure 3.3
Yes
Finish
where,
l.?.n
Core Cll
As described in Section 4.1.2.5., for reactor core 1, the ratio of thc U02-
Gd2s m:ixture to the Zr-4 atru.ctural material i e thed. However, the
U02f'Gd20a is a variable design parameter. Thua the wt%Gd203 in the
U02-Gd203 fuel mixture is known upon completion of the design procedure.
The volume fraction U02 within the U02-Gd203 fuel mi"tw~, Volf(U02), is
given by,
Volt(U02) = - - - - - - - - - - - - (4.43)
1 + PUO! ( 100 _ l)
PGd2 0 3 1 - wt%Gd2J
The corresponding volume fraction within this fuel mixture is given by,
(4.44)
Volc(Gd23) =Vol~Gd2aJVolm(fueli ~ -, )
'tr+ 2 tc+w (4.46)
127
Cores (2.3.4.5)
For reactor cores 2,3,4 and 5 which utilize a lumped bumable poison
distribution, the ratio of U02 to Zr-4 structural material in the fuel meat
and the tbickneas of the bumable poiaon (Gd:a{)a) plate lumps are design
variables. Thus, upon completion of the design proeedure outline in Section
4.3, the uo2 volume fraction in the fuel meat and tbe bumable poison lump
thicknesa ~re known. The whole core volume fractions for U02 cmd Gd20a
are given by the following equations.
where,
128
To estimate the reactivit1 cbange caused by an increase in fuel
temperature, EPRI-Cell was run with the fuel temperature specified by the
resonance data input parameter P.es(1,J) waa decreased to 293C room
temperature (&e Appendii E.) As stated in this appendix, the fuel
operating temperature was set at U>00C. For each reactor core, the
reactivity change for a fuel temperature increase at B.O.C. and E.O.C. ie
given by the following equation,
kett(~C) - 1
ken( 1()()()0C)- 1
PT = keft(293"C) - keft(1()()()0C) (4.49)
129
As stated in Chapter 1, thermal-hydraulics considerations are
assumed not to be limiting for the reactor designe modeled in this study. A
simplified tbermal-bydraulic analyeis, however, haa been included to verify
that fuel element temperaturea are within acceptable bounds and that the
required coolant tlow ratea needed to remove heat are practical. Figure 4.12
illuatrates the fuel plate and CCM>lant channel geometry to which this
analyaia ia applied.. Below, each of the parameters used in the ensuing
discussion are defined.
130
Wp =Width of fuel plate (m)
Ar = Fuel zone croa..;-oectional area (m2)
Aw = Flow area of coolant channel (m2)
Pt. :: Heated perimeter of coolant channel (m)
Pw = Wetted perimeter of coolant channel (m)
l>b = Hydraulic diameter of coolant cbannel (m)
De = Equivalent diam.eter
H = Heigbt of reactor core (m)
Re = Reynolds number (dimensionless)
Pr = Prandtl number (dimensionless)
Nu = Nusselt number (dimensionleas)
v =Coolant velocity (m/s2)
T _ q'"max,m tr 'Ib
co- h +
(4.52)
._T q"'max,m te f
Tc1- co+ kc
(4.53)
131
111
q mu.m
tr2
Tfc =Tfa + 4kr (4.54)
(4.55)
1
The maximum power density in the fuel meat, q" max,m is determ.ined by
the relation,
...
q "' _ q ma][
ma][,m- Volc(meat)) (4.56)
where q"'mu ie detennined by Equation 4.27b and representa the fuel cell
averaged maximum power density. The value of the fuel meat volume
fraction, Volc(meat), ia given for reactor core 1 by,
Volc(meat) = (
tr+ 2tc+tw
!;r , )
(4.57)
Volc(meat) = ( ~ , YN NrN)
,tr+ 2te+ twA r+ t (4.58)
132
Clad F\J.el Clad Coolant Clad Ft.el Clad
For reactor cores 1 and ~ which utilize caramel type fuel, the medium
from fuel surface to fuel center-line is solid uo2 (i.e., through a fuel platelet
as shown in Figure 3.1). Thus only the thermal conductivity of U02 is
needed. However, for reactor cores 3,4 and 5 which utilize a cennet type
fuel, the medi um from fuel surface to fuel center-line consists of U02
particles and Zr-4 structural material. For this type of fuel, the net thennal
conductivity can be estimated by the following correlation,
133
(4.59)
where kp and lr.m are the thermal condu.cti.vitiea oC the U02 particlee and
Zr-4 structural material reepectively.[18] The valuea of (a) and (b) are
defined by the follo'Wing relationa.
a 3km
2km+k., (4.60)
b= Vol%m(U<>2)
Vol%m(Zr-4) + Vol%m(U<>2) (4.61)
I
q max =q flt ... I'
max,m"' Wp (4.63)
134
subatitutiq Equation 4.63 into Equation 4.62 and integrating from H/2 to ..
H/2 yielda,
(4.64)
wherA q is tbe total heat rate tranaferred to the coolant in the hot channel.
The heat rate removed by the coolant is given by,
From continuity,
m=pAwv (4.66)
where,
Aw=twwp (4.67)
Substituting Equations 4.66 and 4.67 into 4.68 and rearranging yields the
required maximum coolant velocity for the reactor core.
V= q
pAw Cp (Tout - Tinluot Channel (4.68)
135
where Nu, Re, and Pr are the Nuaaelt, Reynolds and Prandtl numbeTs
respectively which are defined below.
Nu=~
k (4.70)
(4.71)
Pr = CpU
k (4.72)
(4.73)
(4.74)
1\ =2wp (4.75)
136
The tero~ De is the equivalent diameter of the coolant channel and is defi.ned
(4.76)
Pw=2Wp+2tw (4.77)
137
Thia chapter preaents the resulta of the calculationa described in
Chapter 4 for each reactor core design. A detailed tabular summary of all
calculated resulta ia presented in Appendix F.
Figure 5.1 to 5.5 are plots ofk.etr= f(t) for reactor cores 1,2,3,4 and 5
which are summarized in Table 4.1. each excess reactivity profile satisfies
the constraint of Table 4.2.
138
and 5. The tbiclt lump providea aufticient aelf-ahielding near B.O.C. such
tbat the net uranium depletion ia larger than the net Gd20a depletion thus
reaultiog in exce88 reactivity decreaae.
Tbe Xe135 buildup etreet on exce88 reactivity is not observed in Figure
5.1 which representa reactor core 1. In thia case, the uniformly distributed
gadolinia depletea rapidly at B.O.C. (i.e., no self-shielding effects) causing
an addition of positive reactivity which overridee the negative reactivity
addition caused by the buildup ofXel36.
During the core refuel:ing litetime, a peak in excess reactivity occurs as
observed in Figures 6.1 to 5.5. At this point, positive reactivity addition due
to Gd2s depletion ia equal to the negative reactivity addition due to
uranium depletion. Since reactor core 1 utilizes a uniform Gd203
distribution, this peak occur near B.O.C. while for reactor cores 2,3,4 and 5
which utilize a lumped Gd203 distribution, it occurs near E.O.C.
The importance ofthe reduction ofB.O.C. reactivity by the addition of
the burnable poison Gd203 is readily observed in Figure 5.1 (core 1) and
Figure 5.3 (core 2) which utilize a unorm and a lumped Gd20a distribution
respectively. In these figures, the straight sections of the excess reactivity
curves near E.O.C. are extrapolated to B.O.C. as illustrated by the sloped
dashed line. For reactor core 1, thia extrapolation yields a B.O.C. keff value
of approximately 1.206 without B.O.C. Gd2<)3 reactivity control. By
inspection of Figures 5.2 to 5.5, Xel3li buildup reduces B.O.C. keffby about
0.015. Combining this value with the extrapolatior.. value yields a B.O.C.
keff value of about 1.22. The reactivity peak with Gd20a corresponds to a ketr
value of 1.8. Although the uae of the Gd203 bumable poison is not required
in this case since the B.O.C. ketrvalue remains less than 1.24, it has the
desirable effect of reducing the required control swing, Akeft', from 1.24 to 1.8.
139
The necessity of the reduction of B.O.C. reactivity by the addition of the
bumable poison Gd203 is seen in Figure 5.3, the excess reactivity curve for
reactor core 3. Extrapolating the E.O.C, straight section of the curve back to
B.O.C. (illustratec by the sloped dashed line) yields a keff value aoove 1.28
(this extrapolation can also be done for reactor cores 2,4, and 5). A reactor
core with such a large excess reactivity would be, for practical purposes,
impossible to control. Thus the use ofbumable poison to control B.O.C.
excesa reactivity is essential.
140
1.28
1.26
1.24
1.22 -
1, ..
1.20 ... ,
~ .... ~
1.11
r - --...
~
1.16
1
I L ~ r--....
k-eff
1.14
-......
~
--
1.12
~
1.10
~
-...........
1.01
1.06
~
-~
-..........
1.()4 h ~
1.02
1.00
0.98
o 100 200 300 400 soo tiOO
'11me(da,a)
00"1
un
t()"[
~
~
9(rt
~
L tcn
v
/ on ~
/
/
tn -
"'11:7'
/ tl'l
JPl(
/ 91"1
_., / sn
~
-!'--- -- v
v
ot"l
t:Z"I
nr
9t"l
St"l
1.28
''
1.26 '
' '~
1.24 .... ,
1.22
' ...
''
1.20 ' .. ....
!",
~ ....
1.18
1.16
L ~
1.14
/
/
.~
ket / "'
- 1.12
'
~
~ 1.10
1.08
/
v
/ ""
" ~
1.06
1.04
k. ~
"'
~.i
I
1.02
1.00
0.98
o 100 200 300 400 soo 600 100 800 900 1()()() 1100 1200
Thne(days)
1.26
~
1.24
L ~
1.22
/
/
1.20
1.18
v
1.16
/
v
-t
....
)(.
1.14
1.12
~
/
~
1.10
/
/
1.08
L
V"
~
1.06
1.04
\... - ~
1.02
1.00
0.98
o 100 :.m 300 400 ~ 600 700 800 900 1000 1100 lnt
'Itme(daya)
1.26
1.24
1.22
1.20
~ -~
/
1.18
v
/
~'
1.16
1.14
v '
k-Eif / i
-..
VI
i.12
/
'ti'
1.10
1.08
/ v
..,..,. ~
1.06
____., V'
1.04
1.02 -
1.00
0.98
o 100 Dl 300 400 500 600 700 800 900 1000 1100 1200
'11me(days)
1.26
.
1.24
4th plate, 1.01 core Vol'f,(gadollnia' I--
I I I I
1.22
8th plte, t.79 C:on v~olinia\
.
"Y " "-
\v
1.20
/""
~
UfJ
7' ~
-
kefr
1.16
1.14
1.12
.
.
/
v \
\ /
-, ~
~
/
" ~
~~
~ 7 ~
1.10
7 v ' ~~
1.08
1.06
.
_,/"
v ~
/
~
1.04
l. -
1.02
1.00
.
0.98 .
o 100 3X) 300 400 500 600 700 800 900 1000 1100 1200
'Dme(days)
the reactivity peak is suppressed and also pushed closer to E.O.C. The
increased self-shielding effect causes the net amount of bumable poison in
the core to deplete more slowly. Second, the net amount of bumable poison
in the coreis increased without suppressing the B.O.C. keff value (excess
reactivity) below the minimum allowed value of 1.04. (The value of 1.04 is
set to allow for Xe135 override capability). As with the first effect, the
increase in the net mass of Gd203 is possible due to the increased self-
shielding effect which resulta in a slower Gd203 depletion rate. Thus with
the conclusions derived from Figure 5.6, it is obvious that the reactivity peak
of Figure 5.2 can be suppressed with increased lumping. For purposes of
147
this study, however, this was not possible due to the limit in the number of
space point and zonea tbat can be modeled by the EPRI-Cell code.
With a more sophisticated distribution or/and the use of other burnable
poisons it may be possible to levei the excess reactivity curve of F!gures 5.1 to
5.5. In such a case, the rate of poliitive reactivity addition caused by Gd203
depleon and the rate of negave reactivity addition caused by uranium
depletion are equal throughout the refueling lifetime of the reactor core.
This is what is done in an actual reactor.
148
the mechanically allowable bumup of 60,000MWd/T can not be obtained.
The core refueling lifetime for this core (600FPD) is thus reactivity limited. Reactor
core 2 also uses the caramel fuel design and is thus allowed a maximum
bumup of 60,000MWd/T as liste'-' in Table 4.2. A calculated bumup value of
62J20MWd/T was obtained. The excess reactivity curve for this core (Figure
5.2) shows an E.O.C. value of ketf =1.19 where the minimum value for keff is
1.04. Thus the refueling lifetime for this oore is not reactivity limited, rather
it is limited by the structural mechanics of the fuel. As discussed in Section
3.1.1, internai fission gas pressure will cause fuel failure ata burnup greater
149
Table 5.1. Core bumup data
B.O.C.
Akeff (fuel temp) ~.027 -0.019 -0.0025 ~.00053 -0.00065
B.O.C.
-0.027 -~).021 -0.030 -0.017 -0.018
k. 8 rr(void)
E.O.C.
Akeff (fuel temp) -0.026 -{).022 -0.007 -0.0043 -0.0051
E.O.C.
Ak 8 rr(void) -0.038 -0.028 -0.030 -0.025 -0.033
lq)
Table 5.2 summarizes the B.O.C. and E.O.C. temperature and void
coefficients of reactivity for each rea.ctor core deaign. AB required, the
values are negative in ali cases. lt can be seen that the B.O.C. and E.O.C.
temperatura coefficients of reactivity decrease with increase in uranium
enrichment. This is due to the decrease in the lJ238 concentration. The
effective neutron absorption cro88-section of lJ238 increases with
temperature by a phenomenon known as Doppler broadening. this is
discussed in detail in Reference [7].
In Section 4.6, it was stated that the selection {guess) of the value of
q'"avetr automatically set Vcore by which the core height and radius can be
determined. Table 5.3 summarizes the power maximum and average
power densities and associated core dimensione for each reactor core. The
core refueling times, tn, and fuel meat U02 volume percents, Vol%m(U02)
are also listed in Table 5.3.
Since the net lJ235loading islarger for reactor core 2 whlch is fuel with
20% enriched unmiwn than for reactor core 3 which ia fueled with 97.3%
enriched uranium, Vc:ore is larger for core 2 (667L) than for core 3 (265L).
Both cores operate with the same refueling lifetime of 1200FPD.
Although the U235 loading is smaller for reactor core 1 which is fueled
with 7% enriched uranium than for reactor core 2, Vcore ia smaller for core 1
(506L) than for l:Ore 2 (667L). This resulta since the refueling lifetime for
,..,.1
Table LS. Core dimenaiona and power densities.
reactor coi'E!l is 600FPD while for reactor core 2 it is 1200FPD. Thus reactor
core 1 consumes ha1f as much uranium as reactor core 2.
For reactor cores 4 md 5 which are fueled with 97.3% enriched uranium
and which also operate with refueling lifetimes of 1200FPD, the calculated
values for Vcore are 385L and 333L respectJ.vely. These values for Vcore are
larger than Vcore for reactor core 3 which io al90 fueled fueled with 97.3%
enriched uranium and operated with a refueling lifetime of 1200FPD. The
larger volumes of reactor cores 4 and 5 compareci to core 3 is caused by the ia
caused by the thinner fuel plates used by these cores. For a reactor core of
constant ura:nium mass inventory, as the thickness of the fuel plates ia
decreased, a more homogeneous system is obtained. This resulta in a core
reactivity decrease which, in thia case, ia compensated for by an increase in
Vcore This topic ia discuued in detail in Reference [25].
The associated reactor core dimensions range from 88cm to 65cm and
108cm to 79cm for the core diameters and heights respectively. This
representa net differences of 29cm in height and 23cm in diameter.
Based on the calculated reactor core diameter values liated in Table 5.3,
and the associated fuel element lattice cross-sectional areaa listed in Table
3.2, the fuel element core grid layouta of Figure 5. 7 were estimated. Figures
5.la, 5.lb, 5.lcp 5.ld and 5.1e represent the esti:mated core grids for reactor
cores 1, 2, 3, 4, and 5 respectively. Each square in the figures representa a
fuel element
For reactor core 2 which ia fueled with 20% enriched uranium, a mass
of 193kg U23S i5 required while a mass of 106kg U235 is required for reactor
core 3, where both operate with trf of 1200FPD. Reactor core 2 requires the
larger U236 in order to provide sufficient positive reactivity in order to
override the negativa reactivity added by the increased UZJS mass.
The calculated values of q"'ave,r for each reactor core satisfy the
conatraints liated in Table 4.2.
I '1
&
h
Core 1 Core 2
"
Core3
I
d. ~
Core4 Core 5
155
Table 5.4. '11lermal-hydraulic data.
conductivity of the fuel meat. This high thermal conductivity resulte from
the cermet fuel design were the volume percent in the fuel meat~
156
Table 5.5 enmmarizea the whole core B.O.C. and E.O.C. materiais data.
calculated by the methods described in Section 4. 1.4. which have been
calculated for raference p\li"))Ollea. The E.O.C. enriehment ia the
percentap of tJ236 which ia contained in the total E.O.C. uranium mass
(i.e, the aum ofthe E.O.C. mauea oflJ233, tJ236 and 1J238).
Figurea 6.8 to 5.12 are plota over the refuel.ing lifetime ofthe plutonium.
mass contained in reactor cores 1, 2, 3, 4 and 5 reapectively. Plutonium
buildup resulta from the conversion ofU238 to Pu239, which in turn is
converted to Pu240, Pu241 and Pu242. Reactor core 1 which utilizes 7%
enriched uranium contains lesa plutonium than reactor core 2 which is
fueled with 20% enriched uranium since it haa a refueling lifetime half
that of core 2. For reactor core 3, Figure 5.10 indicates that the total mas a of
plutonium in the core decreases near E.O.C. Thia results since the U238
concent.ration has been depleted to an extent that Pu 239 production is lesa
than the consumption cf Pu isotopes by fiBSion or conversion to higher
actinides.
157
Table U Core materiais data.
158
\
\
\
~
\ \ ~
~
....8
12:
~ ~
;>
a~
\ 3
- --
::1
,_
!\
0..
\ ~li
i .....t
'-"
G:l
~
o(.)
~ ~ ....
.s
t)
\\ ~
~
cu
~ a
\ l
!
\ 8
-
fZ
\ __
,
. . .
""' . Q
159
~
-
\ 8....
...
1\\
- .
G,)
\ !j
e
'.::3
\ i
>
a:i
9
\ ~
a
3
- -=..
'a
\ I C'l1
........
f
' 8
\ ~
...
~:~
'\
~
.
~
'
"'1\ ~ j
~
'\ ~
-
8
"
. . . .
"
160
~
-
1/
1/ -
8
....
- Q)
.
~ .o8.
11)
>
r;
a
\ -
.s::s
~
~
- -
i --
t:l.
A
C'f':)
Q)
\
J.o
oCJ
\ ~ lo-4
~ ~Cl
\ ~
~ .
'
~ =
'1""4
"~
at5
~ 1
" ~ ~
~
"' ~
""
' -
8
C"1
o -
c::i
"' ~
c
o
o
1 h1
-
-
8
-
\ i
~
8
:0
\ >
..;
a~
~
~
\ ~
s:::1
-a
\\
~ I .s
---'
f
\ ~
8
...
u
CXJ
1\ ~
~
....
,...
1\ ~
~
j
~ .
~
~ [\._
-8
"~
V"l
o
~
o a C"1
o -
d
C!
o
o
f
162
~
-
-
-
8
- .
\ ~
e
(I)
""""
~
\\ >
Cll
a~
\ .s
--
~
~ 'a
\ \
~
I
..-.....
1.0
f
8
...
\ ~
.su
ca
\ ~
~ ~ c4
'\ .-4
at5
~ ~ !
"i', r::
~
""' "
~
~
-
8
o
.,..,
o d C"''
c:i
N
o -
d ~
~
~
163
AB di8CU.81Jed in Section 4.1.2.5, the hydrogen nnd oxygen number
density values specified in the EPRI-Cell input files for ali reactor core
designa were calculated baaed on the density of water at room temperature
rather than at the ave:age reocior coolant temperature of 305C. The
density ofwater at room temperature (20C) is lglcm3 while at 305C it is
O. 74g/cm3. The Equationa uaed to caiculate the hydrogen and oxygen
number densities are listed below.
The number density ofthe H2<) molecule is given by)
N(H2) = p(H:tJXNA)
M(H2l102-fbams/cm2) (4.23)
where the associated H2 properties are listed in Table 2.8. The number
densities ofthe hydrogen and oxygen constituents are given by,
(4.24)
(4.25)
164
neutron absorption properties decreases the thermal neutron population.
Consequently, a decrease in coolant water density must be offset with an
increase in Vcore in arder to maintain constant core excess reactivity with
ali other core materiais volume fractions remaining nnchanged. As a
reault, an increase in Vcore for constant refueling time will result in a
decrease in the values of q"'ave,r B2 and BU. Ao increase in Vcore will
also cause an increase in the total mass of materiais present in each core
which are calculated by Equation 4.42.
In this section an estimated correction factor for Vcore. which ia
applicable to each core considered for ia study, is derived using an
approximate 2-group diffusion analysis. The general multigroup neutron
diffusion equation solved is,
(5.2)
where,
G
~g =L~~g + L L~~g'
g'=l (5.3)
165
The terma used in Equations 5.2 and 5.3 are defined below.
Solving Equation 5.2 for with = keff for two neutron energy groups
yields,
k ff = VI.f2:21 + V:,fl
2 2
e (DtB 2 + Iat + IuXD2B + :Ea2) (DtB + I.at + I:u) (5.4)
For purposes of this analysie it ia assumed that :12 (scattering from the
thermal to the fast energy group) is equal to zero since it is sufficiently
small. Also since most fission neutrons are bom into the fast energy
group, it is assumed that 11 = 1 and 12 =O. These considerations are
further explained in Reference [Henry]. The diffusion coefficient D is
defined by the following relation,
166
Dr=a~ (5.5)
where,
Each macroscopic crose-section used in Equations 5.2 and 5.3 are the
sum of the contributions of the macroecopic cross section cf water and the
macroscopic cross-section of ali non-coolant materiais present in the
reactor. Thus Itrt, Ur2 Lat, La2 and l:21 are defined as,
(5.6a)
(5.6b)
(5.6c)
(5.6d)
(5.6e)
11\7
Equations 5.6a and 5,6b into Equation 5.4 and Equations 5.6c, 5.6d and 5.6e
into Equation 5.6 the followi.ng result is obtained.
"~(Dm) + Dw))B 2
+ I,dm) + ld'w~)
(5.7)
168
4
I, ~I) ~I) (H)
11'1=1
Oxt(H) ~ ..;..-~-----
4
I, ~I)
pl (5.8)
4
l: q,) Ox{e) (O)
pl
o)
0':.:1( = ..;..._-.----
L~~>
pl (5.9)
(5.10)
(5.11)
The core averaged macroocopic cross-sections for oxygen and hydrogen are
then determined by the follcwing equatiom.
169
Id<H2) = Volc(<Jd{H)N(H) + <Jd{O)N(O)) (5.13)
where the hydrogen and oxygen number denaities. N(H) and N(O), are
listed in the zone homogenized numbeT densitiea of the EPRICell output
file ofSection E.4. The multiplying factor Volc(H20), which is the H20
volume fraction (volume percent divided by 100) in the core, muBt be include
since the microscopic crosssectiona are not core averaged. The core H20
volume fraction is given by,
4
L ~g) l:x(g)
~ g=l
Loz.l = --.---
L ~g)
g=l (5.15)
170
The thermal group macroscopic cross sections are given by the relation,
(5.17)
(5.18)
(5.19)
The values of I.21 can not be calculated directly from the cross-section
data listed in the EPRI-Cell output file. The scattering cross-sections listed
include ingroup scattering acr::ording to the following equation.
(5.20)
which is used to determine l:u. Subatituting this value into Equation 5.20,
I21 ia determined by,
171
Ia1 I.1 .. I.u (5.22)
(4.37)
where
R-~~
-v 2.5i (4.35)
and
H=2.5R (4.36)
172
The data calculated uaing the techniques deacribed above and the
associated values are listed below.
Lal(m) = 0.0145cm 1
l:8 t(W) = 0.00017cm-1
l:a2(m) =0.3642cm-l
l:a2(w) =0.00547cm-l
Ltrt<m) = 0.1367cm-1
~trl(w) =0.1872cm-l
Ltr2(m) = 0.3436cnrl
I:triw) = 0.7572cnrl
D1(m) = 2.483cm
Dt(W) = 1.781cm
D2(m) =0.9700cm
D:l{w) =0.4402cm
VLfl =0.0187cml
v In = 0.4876cnrl
l:u(w) = 0.45393cm-l
I.at(w) =0.46149cnrl
Lri(W) = 0.07071cm.-l
I.n(w) = 0.38322cnrl
l:2t(W) = 0.07827cnrl
B2 = 0.00533cm2
173
To determine the effect of a reductit~~n in coolant density on Vcore,
Equation 5. 7 ie rewritten as,
(5.23)
where,
Substituting a value for fw =0.75 into Equation 5.23 along with the
calculated values for the other parameters Equation 5.23 is solved via
iteration for fs. The para.meter fa is the approximate fraction by which the
geometric buckling of each reactor core must be decreased in order to
maintain constant reactivity. As evident from Equations 4.36 and 4.37, f ais
proportional to the in verse square of fR (fraction by which the core radius
must be increased) by the following relation,
(5.24)
174
Solving Equation 5.24 for fa yielda,
fa={& (5.25)
By Equation 4.35 the correction multiplier, fv, for Vcore is given by,
fv = (fa)3 (5.26)
fq =_l_
fv (5.27)
(5.28)
The correction multiplier, fm, for the net core material masses which are
listed in Table 5.4 ia given by,
(5.29)
The values for the approximate correction factors are listed in Table 5.6.
175
Table 5..8. Approximate correction multipliers.
fs 0.90
fR 1.05
fH 1.05
fv 1.17
fq 0.85
fsu 0.85
fm 1.17
176
CB.API.'ER 8
CoacJwdon aad BecommendGtiODI
6.1 CoDclutdon
AB stated earlier, it is known that modem U.S. are fueled with very
highly enriched uranium; greater than 90111. In this study, a reactor core
using plate type fuel elementa fueled with 97.3% enriched uranium which
operates with a refueli.ng lifetime oi 1200FPD, waa m.odeled. The safety
coeffi.cienta of reactivity and thermal hydraulics resulta calculated are
acceptable.
The French have proved that the use of LEU (i.e., approx:imately 7%
enriched uraniu.m) as a nuclear submarine fuel is feasible. In this study a
reactor core uaing plate type fuel elementa fueled with 7% was enriched
hl'BDium was modeled. However, it was not possible for this core to
maintain criticality beyond a refueling lifetime of approx:imately 600FPD.
Also for thia case, the aafety coefficient of reactivity and thermal hydraulics
are acceptable. Tbe volume of tbis core is roughly twice the size of the core
fueled with 97.35 enriched uranium. This corresponds to a 17cm and 20cm
increase in diameter and height respectively (these dimensione are
corre,:ted using correction facton of Table 5.6) .
A reador core using plate type fuel elements fueled with 20% enriched
uranium which operates with a refueling lifetime of 1200FPD, was
modeled. The safety coefticient of reactivity and thermal hydraulics differ
very little compared to the core fueled with 97.3% enriched uranium. AB
discussed in Chapter 1, low enriched uranium, LEU, is intcmationally
regarded to be u.ranium with enrichment in the range0%- 20%. Thus it is
177
demonstrated that a reactor core using LEU and with operating
performance similar to the 97.3% enriched core, can be designed. The core
fuel with 20% enriched uranium is, however, about two and one half times
largar than the core fueled with 97.3% enriched uranium. This
corresponds to a 24cm and 30cm inaease in diameter and height
respectively (these dimensions are corrected using correction factors of
Table 5.6). Thua as maintained in Chapter 1, these dimensional increases
are sufficiently amall that they can eaaily be compensated for by the use of
an integral reactor design.
178
For each reactor core modeled in this study using one dimensional
calculations, a more detailed analysis can be done which accounts for
spatial dependence of fuel deple.on, control rod motion and startup,
shutdown and transient bebavior.
The DIF3D code developed by Argonne National Laboratory can be used
to model, with 3AD di..ffusion theory, the steady-stat.e behavior of each reactor
core. DIF3D solves multigroup diffusion theory eigenvalue, adjoint, fixed
source and criticality (concentration search) problema in 1-, 2- and 3-space
dimensions for for orthogonal (rectangular and cylindrical), triangular
and hexagonal geometries.[26] The reactor core fuel element grids
illustrated in Figure 5,1 and dimensions ofTable 3.2 can be used in
preparation of a DIF3D input file. The core heights listed in Table 5.5 can
aloo be used. (Note that these dimensions must be corrected using the
correction factors listed in Table 5.6). The EPRI-Cell input files used for
this study are set up to produce 5-group cross-section data in ISOTXS data
seta (see Appendix E) which can be input directly into DIF3D.
To model the time dependant aspecta of the fuel cycle of each reactor
core, the REBUS-3 fuel cycle analysis code, also developed by Argonne
National Laboratory, can be used. AB in the above case the corrected
dimensional data deucribed above can be used in preparation of a REBUS-3
input file. There are four types of of search procedures thRt may be carried
out in order to satisfy user supplied constraints.[27]
179
1) Adjustment of the reaetor refueling lifetime in order to achleve a
apeci.fied E.O.C. fuel bumup.
Also, for REBUS.3, the 5-group cross-section data listed in the ISOTXS
data seta can be input directly.
For thennal hydraulic transient analysis, the P ARET code developed by
the Phillips Petroleu.m Company, can be used. PARET is a digital
computer program designed for use in predicting the course and
consequences of nondestructive reactivity accidents in smail reactor cores.
This code couples neutronics and thermal hydraulics and uses point
kinetics, 1-D hydrodynamics and 1-D heat tnmsfer.[28]
1RO
[1] Cochran, Thomas B., Arlrin, William M., Norris, Robert S., Hoenig,
Milton M., Nuclear Weapona Data Book, Volume 11, U.S. Nuclear
Warhead Production, Ballinger Publishing Company, Cambridge,
Massachusetts, 1987.
[3] Nuclear Theft: Risks and Safeguards, A Report to the Energy Policy
Project of the Ford Fot' iation, Manson Willrich, Theodore B.
Taylor, Ballinger Publishing Company, Cambridge, Mass, 1974,
Pg. 228.
181
[7] Lamarsh, John R., Introduction to Nuclear Engineering (2nd
Edition), Addison-Wealey publishing Company, Reading,
Maasachusetts, 1983.
I R?.
[13] Barnier, M., Baylot,J.P., Oeiria, A M.TR Adopted and Well Fitted to
LEU Utilization, Qualifieation and Development, Experimental
Reacton Department, Saclay Nuclear Center, France, As Presented
in, JAERI-M 80-073, Proceed.ings of the Intemational Meeting on
Reduced Enrichment for Reaearch and Teat Reactors, October
24-27, 1983, Tokai, ,lapan, May 1984.
[17] Kaunan, Albert F., Nuclear Reactor Fuel Elemcnts, Metallurgy and
F~brication, John Wiley & Sons, N.Y., 1962.
183
[19] Copeland, G.L., Hohba, R.W., Hofman. G.L., Snelgrov, J.L.,
Performance of Low-Enriched U3Si2- Aluminum Dispersion Fuel in
t...'te Oak Ridge Rasean:h Reactor, Argonne National Laboratory,
ANl/RERTIVI'M-10, October, 1987.
[23] Rahn, Frank J., Adamantiades, Achilles G., Kenton, John E.,
Braun, Chaim, (of the Electric Power Research of California), A
Guide to Nuclear Power Technology, A resource for Decision
Making, John Wiley & Sons, N.Y. 1984, Pg 437.
184
[26] ANJ..,..82-64, DIF3D: ACode to Solve One-, Two-, and Three~
[27] A.NL-83-2, A U ser's Guide for the REBUS-3 Fuel Cycle Analysis
Capability, B.J. Toppel, Applied Physics Division, Argonne
National Laboratory, 9700 South Cass Avenue, Argonne
Dlinois, 60439, March, 1983, Prepared for the U.S. Department
ofEnergy.
185
[31] Nero, Anthony B. Jr., A Guidebook to Nuclear Resctors, Fuel Cycles,
The Iaauea of Nuclear Power, Univeraity of Califomia Presa, Los
Angeles, 1979.
186
AppendixA
Non-Proliferati.on Treaty and Fornign Nuclear Objectives
Modem day concerns are not only with the continued diffuson of
information related to he design of nuclear weapona, but also with the
increasing availability of the technology to produce weapons usable
materiais. To date there are five "official" nuclear weapons states (NWS),
the U.S., the U.S.S.R., the U.K., France and China. However, Israel, South
Mrica and Pakistan are widely believed to have the capability to produce
nuclear weapons, while lndia detonated a peaceful nuclear exploaion (PNE)
in 1974.
Relatively early on in the nuclear age, pressure began to develop for an
inter-national agreement to thwart both the vertical and especia1ly ~ he
hori7ontal proliferation of nuclear weapons. (Horizontal proliferation refers
to an increase in the number of states possessing nuclear weapons, while
vertical proliferation refers to the growth in the nuclear arsenais of the five
nuclear weapons states.)
Consequently, in June 1958, lreland submitted to the UN General
Assembly, a resolution.-requesting the establishment of a committee to
study the dangers inherent in the further dissemination of nuclear
weapons. This resolution did not deal specifically with horizontal
proliferation; however it recognized the possibility that an increase in the
nurnber of nuclear weapons states may occur. Following mount.ing
concern by the international community, the title Non-Proliferation of
Nuclear Weapons was adopted in 1965 by the UN General Assembly in a
resolution calling on the Eighteen Nation Disarmament Committee (ENDC)
to lay the foundation for such a treaty. After intense negotiations between
187
the US and the USSR, final draft.a of a treaty were aubm.itted at the UN .[29]
Upon further reviaiona by the ENDC the Non-Proliferation of Nuclear
Weaponat Treaty waa aigned in June 1968. A central element of the Treaty
is a syatem of safeguarda to be administered by the Vienna based
Intemational Atomic Energy Agency (IAEA), which waa established in
1957. The objective of the safeguards ayatem ia to verify that nuclear
materiais used for peaceful activitiea in NNWS ia not diverted to the
production of nuclear weapons.
Since it eu~i-ed into force in March of 1970, 135 natione have signed the
treaty, including three of the five nuclear weapons states. France and China
refused to aign, along with a number of NNWS auch as Argentina, Brazil,
India, Israel, Pakistan and South Africa. Thia brings to light an inherent
weakness in the non-prolifemtion regime; not ali of the significant NNWS
are members.[30] Thia waa further demonstrated by the indigenous
acquisition of a nuclear explosive by lndia in 1974 as evidenced by its so called
"peaceful nuclear explosion". In ita attainment of a nuclear explosive
capability, India aet a precedent; none of the other NWS had reached this
status via commercial nuclear development, rather the converse is true:
commercial nuclear development was based, in part. on previoua military
work.[31] Since lndia is not an NPI' signatory, it could clairn to have violated
neither the Treaty'a prohibition of ali nuclear explosive devices or explosive
use of nuclear material supplied by other nations. However, Canada did
claim that India violated its pledge not use a Canadian supplied research
reactor to produce the plutonium for the PNE.
Another perceived weakness of the NPr is the nonrequirement of
safeguards for nuclear material used for maritime nuclear propulsion,
including its military application. This was intended by the Treaty's
188
draftera. In the 1960&, aeveral NATO membera, including ltaly and the
Netherlanda, were activeJy conaidering the acquisition of nuclear powered
shlps and demanded an ezclu&ion for nuclear propulsion.[29] As a result,
it ia penniaaible under Paragraph 14 of the IAEA model safeguards
agreement INFCIRCL153 10 to withdraw from IAEA safeguards, nuclear
fuel when it is uaed in non--e.zploaive military applications such as fuel for
submarina reactora.[30] Tbe NPI' only uaigna the IAEA the obligation of
applying aafeguards to nuclear materiais in use for peaceful activities such
as that used in research or commercial reactora. However, to date, no
NNWS has availed itaelf to this ezemption to the rule that all nuclear
material in NPr NNWS is subjected to safeguards.
To date, only the five members of the official nuclear weapons club have
developed the technology to build nuclear powered submarines (SSN s).
However, in December 1987, lndia "leased" an SSN of the Charlie class
from the Soviet Union, making it the first ever NNWS to opera te this type of
submarine.[32] The NPT and associated IAEA system of safeguards did
not prohibit this transfer on either the part of the Soviets or India.[33] A
related development occurred in June 1987, when Canada, a long time
supporter of non-proliferation, announced planes to acquire a fleet on 10-12
SSNs. Since Canada has impeccable non-proliferation crdentials, there
was little concem that it would utilize the safeguards exemption to divert
enriched uranium for weapons. However, some analysts thought that it
would set an unfortunate precedent in this regard. However, Canada
sought to alloy these concems by decla.ring that it would enter into a
bilateral monitoring arrangement with its supplier w cover the period
during which the material is not subject to IAEA safeguards.
Another problem is that st.ates such aa Brazil may seek to justify the
189
development of an indigenous uranium enrichment eapability by the
requirement for enriched uranium for nuclear submarine reactor fuel.
The potential for nuclear weapona development existe if such a capability
were achieved.
In April 1989, Canada hu since cancelled its SSN acquisition program due to
budgetary conatraint&.
190
AppmdizB
Nuclear MateriaJe Crifblity
and lJ138 where for our purposea, tJl34 ia negligible. The enrichment of
natural uranium or UNat ia 0.711% where enrichment is defined as,
235
mass (U
)
E=---------------------
235 238
mass (U ) + masa ~U ) (B.2)
Fissile iaotopea (0233, {]235, Pu239, Pu241) have alarge fission tToss-section at
thermal neutron energies (i.e., 500b at 0.025eV), while fissionable isotopes
such as Pu241 and U238 have a very low crose-section at such energies. In
fact, the fission cross-section of lJ238 is essentially zero below a neutron
energy of lMeV.
The principal fissile isotopes used in nuclear weapons are lJ235 and
Pu239. Weapons grade uranium and plutoniwn contain greater than 90% of
these isotopes respectively. The actual amounts required for weapons use
depend on the details of a number of factors which are not available to the
general public. However, it is known that the criticai mass (minimum
mass required fcr criticality based on prompt neutrons) of the fissile metal
as a reflected sphere is roughly 5kg for Pu239. and 18kg for lJ235. A possible
reflector in this case is beryllium.
191
About 8q of typical LWR plutonium constitutea a criticai mass when
fab:icated int.o a reOected. sphere.[31] Use of an o:Dde reduces the fissile
atom denaity and increases the criticai masa by appro:a:imately 50%. Such
quMtitiea of theae material& are not very large; i.e., a 4kg sphere of
plutonium ia amaller than a baaeball.[l]
When tbe concentration or enrichment of lJ23S drops below 20%, the
refleeted criticai ma88 becomea prohibitively high, becoming infinite below
about 6%. For Pu239, tbe re0ect4:td criticai mau ia 20kg at 0% fi asile content.
This is illustrated in Figure B.l. Bare unreflected criticai masses are a
factor of three to four times higher.[34].
192
100
80
\
\ .,t
23!i
\ ~
~
Pu239
20
[/
~r ~
---...
-
o .
o 20 40 60 00 100
Fisaile Content (%)
193
The nuclear fiuion cbain reaction can be deacribecl quantitatively in
terma of the neutron multiplication faetor (k). Tbia ia defined as the ratio of
the number of ftsaiona (or fiaaion neutrona) in in one generation to the
number of fiaaiona (or 688ion neutronl) in tbe prec:eding generation.
k -1
p= k efr (C.2)
were reduced, for example, by the insertion of a neutron &bSGrber into the
reactor, the reactivity would be negative. Thus the insertion of a neutron
absorber or control rod corresponds to the insertion of nega tive reactivity. A
194
poaitive reactivity inlertion correeponda to the a chaqe that inc:reaaea the
neutron population auch u replaciq a fuel element with one containing
uranium fuel of a higher enrichment. There are many other changea that
can take placa in a reactor that correapond to the inlertion ofnegative
reac:tivity or poaitive reactivity.
19Cf
For a reactor operating at a tbermal power of P megawatts (MW) and
with a recoverable energy per fission, the rate at which fiasions occur per
second in the entire reactor ia,
8. ul
. . 10 JO ee fiaaion Me V 86,400 sec
Fiaston rate = P MW I MW I M" x x d
-eec 200 ev 1.60:.: 10.13 joule ay
21
= 2.70 I 10 P fissionalday. (D.l)
This can be converted. to grama per day fissioned, which ia also called the
bumup rate.
21 23
Burnup rate = 2.70 x 10 P fissions x 6.023 x 10 atoms x mole
day mole 235 grama 235U
the ratio of the microscopic absorption cross section t.o the microscopic
fission crosa-section,
o.
(1 + a)=o
r (D.3)
IOF..
From Equations D.l and D.3 it follows that,
Since the value of a at thermal energies is 0.169, from Equation D.4, U235 is
consumed at a rate of 1.23g/day for every megawatt of reactor thermal
operating power. The consumption rate however does not represent the
amount of heavy metal destroyed.
Since a reactor operating at lMW for 1 d.ay fissions 1.05 grams of U235,
6
lMWd 10 g
1.05 g X t =S50.000MWdlt
197
AppendixE
EPRI-CELL IDputJOutput Descripti.on
This appendix is divided into four section that together describe the
EPRI-Cell inputJoutput data and process. These sections include an input
description as presented by the EPRI-Cell user's manual, a discussion of
the input data required to satisfy the input parameters needed to perform
the calculations, description and interpretation of the EFRI-Cell output,
and a sample EPRI-Cell output file.
Titles
Alphanwneric titles for EPRI-Cell must precede ali other input cards. The contem of
title cards are as follows:
(1) CARD 1 This is a case title, which may use 80 columns and be in any fonnat.
(2) CARD2 Four character name for each composition K in increasing order.
(20A4 formal)
(3) CARD 3 Four character name for each region in increasing order. ( 1OA4
formar)
(4) CARD4 Four character name for each rone L in increasing order. ( 1OA4
format)
198
Nuclides and Number Densities
The NAMELIST input rcquired to describe lhe initial number densities are listed
below.
(7) NUCLID(J) ZAS LD. for each nuclide present in lhe problem, entered in
increuina onier. The ZAS I.D. for an isotope is detennined from:
(8) TEMPID(I) Temperature lD. for scattering kemel of each nuclide. Allowable
values of ZAS I.D. and temperature I.D. for the current library are
listed in Ta.ble 3.3 of the EPRI-Cell user's manual. eK)
(14) OPTION(3) Group dependent buckling will be used. Array AL2(J) also
required as input
199
(16) OPTION(5) Resoo.ance overlap can:ction applicd. Appropriale for mixed oxide
fuel only.
(18) OJ7fi0N(7) Buckling search: With this option, group constants edited reflect
converged buckling. Note that opnons 7 and 3 may nol be selected
sim~~~sly.
(23) OPTION(12) Edit fast and therrnal microgroup fluxes (thennaJ fluxes are ~u).
(24) ornoN(l3) CINDER numbcr densities printed for each depletable point
(intended only as debug output). Note that only main chain Xe 1JS
and Sm 1.t9 are printed.
(26) OPTION ( 15) Heterogeneous fast effect correction applied. Use~ if the three
innermost zones are fuel, clad and moderator.
(28) OPTION ( 17) Enter OPTION ( 17)=2,3 or 4 indicating the number of collapsed
broad groups to be edited. Table 3.2 of the EPRI~Cell user's
manual defines the energy break:points for lhe standard collapsed
edits. Set=5 for standard 5 group edit.
200
(35) OPTION(2.4) Enter O if timestep lengths input in MWD(fONNE, or l if input in
hou;s.
(36) OPTION(25)
(42) AL2(J) Group dependent buckling for 68 fast groups. U!;e v:hen
OPTION(3)=1, in which case BUCKLG is used as a single value- of
buckling for the thennal group.
(45) PHITYP Ent~r 1.0 for P1 or 0.0 for B-1 fast calculation.
(46) IEDIT(L) Emt indicator for each zone L. Each zone L w'losc edit indicator is
1 is included in the ''edit cell". Extra zooes in a supercell calculation
supercell calculation, IEDIT for the extra region should be O. For a
supercell edi~ IEDIT for the extra regon shauld be l.
(47) LBG(I) First fme group in broad fast group !. The standard 5 group
structure is obtained by inputtin,6 LBG-=1,11,31,63. (DEfAULTS)
(48) I5GT(I) The thennal broad group for each fine thennal gmup. The ~.t.andfu""d
5 group structure is obwbed by inputting ISGT-:~21 *5, 14~~.
(DEFAULTS)
201
(51) TEMP(L) Temperature (K): lf a nuclide is entered whose thennal cross-
sections are determined from doppler-broadened resonance
parameters, (e.g.,Pul<IO, Gd 155 ), TEMP(l) is required. TEMP(3),
required for the 5 or collapsed group edits, Is the moderator
temperature (utilized in the generatioo of the MND diffusion
coefficient).
Geometry Data
(52) NGEOM Set this equal to 1 to invoke slab geometry. Absence of this flag
invokes the stand.ard cylindrical geometry.
(55) ZONECf(l) Depletion indicator for zone I. Use 1 if zone I is depletable or zero
if zone I is depletable.
(56) XTREG Region number or scattering ring, if any. This signals the code that
region number "XTREG" has no physical signi.ficance and is not to
be induded in the thermal flux nonnalization, etc. (DEFAULT=())
Resonance Data
(57) NUCRE Number of nuclides for which resonance data are entered.
(58) IDRES(J) ZAS I.D. number of nuclides for which resonance calculations are
to be done. For each of the nudides listed in IDRES(J), five input
values are required.
(59) RES(l ,1) Resonance temperature in K for the Jlh resonance nuclide.
(60) RES(2,J) The mean chord length Lave. for the absorbing lump where the Jth
nuclide exists. For Lhe fuel cell problem,
4V
Lave =s (E,l)
whcre,
202
(61) RES(3,J) The Dancoff factor, C, for the interaction between lumps containing
the .J1h resonance nuclide.
(62) RES(4)) Tite excess potential scattering cross-section in absorbing lump for
the J1h resonance nuclide. This value in calculated from,
(E.2)
Recommended values for . and <Jp are listed in Table 3.4 of the
EPRI-Cell user's manual.
(63) RES(5,J) Number density of the Jth resonance nuclide in the absorbing lump
where,
203
Variables Used to Designate an ISOTXS Data Set
An ISOIXS data sct must bc cn:atcd in ordcr to allow the input of the EPRI-Cell
generatcd data into DIF3D. (DIF3D is acode usal to solve one, two and three dimensional
diffusion theory problems)
(67) ISOSTP(N) Flag for generation of ISOTXS cross-scctions for timestep N.
=O (DEFAULn Exclude cross-sections for this timestep.
= 1 lnclude aoss-sections for this timestep. Combine the
epithermal and thermal fission products into one fission
product
=2 lnclude cross-section for this timestep. l.eave the epithermal
and thennal ftsSion products as se.parate lumped fission
products.
(68) ISOCS flag to describe bow the epithennal and thermal fission product
cross-sectioos are to be calculated in the ISOTXS data set.
=O (DEFAULT) Write the pseudo cross-sections. These are the
same cross-sections that are printed in the EPRI-Cell output
These pseudo cross-sectioos when multiplied by the
horoogenized concentrations printed in EPRI-Cell give "true"
macroscopic cross-scctions.
= 1 Write the "real" cross-sections. These cross-sections are the
pseudo cross-sections multiplied by the homogenized
concentrations divided by the total fission source per unit
volume. The ECOATA file generated by the EPRI-Cell
contains the pseudo lumped fission product cross-sections,
homogenized concenttations, and total fission source per unit
volume.
(72) HISONM(J) User supplied isotope name to designate lhe isotope in the ISOTXS
data set Isotope names must be in the same order as the Z-\S
nuclide I.D.'s specified in the NUCLID array. (DEFAULT=names
specified in the 111ERMOS library). Blank name designates that
isotope will not be written into the ISOI'XS data set for any time
step.
CARD2 (2) Fow- character name for each composition, in increasing order,
in fuel cell to be roodeled.
GAD = Gadolinia
ZR4 = Zirealov - 4
H20 = Water ..
U02 = Uranium dioxide fucl
CARD4 (4) Four character name for each wne L, in increasing order, in
increasing order.
205
NGEOM (52) Set equal to 1 to invok.c slab gCOilletry (i.e., plate type fuel).
NCOM (.5) Set at 4, (i.e . four compositions in the fuel elemenr, GAD,
ZR4, H20 ANO U02)
NUCLID(J) (7) Thc ZAS I.D. of the 17 nuclides or lumped nuclides present in
the fuel element Each nuclide and its ZAS I.D. are listed
beiow. Note that lhe higher actinides have been neglected for
purposes of this study.
Nuclidc; ZAS ID.
206
Gdl55 641550 Treats lhe isotope GdlSS. Entering
Gctl55 initializes Gdl54, Gdl56,
Qdl58 and Gdl59 in the CINDER
calculation in the natura.lly occwring
proponions. Thus on1y the number
densities of the isotopes Gd ISS and
Gd 157 are entered in the input files,
while the remaining gadolinium
isotopes are teated as a void by the
user.
i-IISONM(n (72) Each input file was set up for the generation o f the ISOTXS
data set soas to allow the option of running DIF3D for a
particular case in the event a more detailed calculation was
deemed necessary. Thus an entry for HISONM was required
for each nuclide in order to designare its existence in the
ISOTXS data set The abbreviation or HISONM chosen for
each each of the 17 nuclides, in order of increasing ZAS I. O.
are, ZR, H, B, O, XE, SM, 0155, G157, U35, U36, U38,
P39, P40, P41, P42, FPI and FP2.
207
TEMPID(J) (8) The values of fc:r this paramcter were selected from TABLE
3.3 of the EPRI-Cell user's manual based on an estimated
average coolant tcmperature d. JO()DC for the coolant, 3800C
for the cladding and 7000C for the fuel. These numbers need
not bc refincd si.nce the current EPRI-Celllibrary contains
roughly 3 to 7 temperatures at which microscopic cross-
section sets are available. The crosssection sets at the
temperatmes closest to those specified above for coolan~,
cladding and fuel were selected.
OlDISO (69) Set at Oin mier to generate a new ISOTXS data set after each
EPRI-CeU run.
ISOTSP(N) (67) Set at 1 for each timestep in order that the cross-sections for
each timestep be included in the ISOTXS data set A value of
l results in the epithennal and thermal fission products being
combined into one fission product.
NTIIBG (70) Default taken resulting in two broad groups in the thennal
region.
NFSBG (71) Default taken resulting in three broad groups in d.e fast
region.
ISOCS (68) Set at 1 by me diiection of Reference [10].
PUREDN(J,K) (9) Design variable which specifies the number densities of each
nuclide in each composition. The number densities in each
fuel zone must be changed with each design calculation.
Number densiti~ in the moderator wne are changed in order
to calculate thc coolant void coefficient of reactivity for a
particular reactor core. 1be calculation of these values is
discusscd in Section 4.1.2.5. These values are read into an
array by the EPRI-Cell code. Array locations not receiving an
entty are set at O by default.
VOLFRC(K,L) (10) Design variable which specifies the volume fractions of each
composition in each zone of the cell and which must be
changed with each calculation. The calculation of these values
is discussed in Section 4.1.2.4. These values are read into an
array by the EPRI-Cell code. Array locations not receiving an
entry are set at Oby default.
OPTION(6) (17) Set at one resulting in lhe space points of a particular
zone be!ng set at equal thickness. The number of space points
is designated by the input parameter ZONEPT(I) where I is the
wne number in the ceU.
OPTION(8) (19) Set at 1 to invoke the analytic isotropic boundary condition.
OPTION(17) (28) Set=S for the standard 5 group edit in the EPRI-Cell output.
Thus tive collapsed broad groups will be edited.
208
OP110N(24) (35) Set=l in order to permit rime steps to be entered in
MWD/fonne.
OPTION(25) (36)
( 0-1-4-20-70-160-250-400-600-800-1000-1200 )
(24.0,72.0,384.0, 1200.0,2*2160.0,3600.0,5*4800.0,)
POWR (39) Design variable specifying the reactor core power density in
Watts/crn of height lts use is discussed in Section 4.1.2.6.
This \'alue is calculated by the following equation,
IEDIT(L) (49) Set= 1 for for each zone to be modelcd in order that dara
calculated for each :wne appear in the output file.
209
TEMP(L) (51) Set=293 f<r each zonc by thc dircction of Reference [10].
WNEPT (53) Tbe EPRI-Cell oode has the capability to handle 6() space
points or intervals. Howevez, on the mM 3033 computer
used for tbis study, cases rwa with greater than 50 space pointl\
resulted in run time errors. Thus tbe number of space points
was kept to SO or below. In mler to pennit lhe modeling of a
maximum IJIDDbcr~late sand coolant channels into one
ce~ spacc. ,...oints in cacb of tbese zones was kept to a
minimum. For fuel p~atcs., 3 space points w~ spxified; thus
approximating the self shielding effect. For burnable poison
plates consisting of solid lumped gadolinium. 7 space points
wc:re specified in mler to modcl the desired self shielding
effect. 1be number of space points in the cladding and
DIOdlerator (coolant cha.rmels) WCR set at l and 2 respectively.
WNETK (54) Design variable specifying the thickness of each zone; fuel
cladding, moderator and also bumable poison.
ZONECI' (55) Set= 1 for fuel and bumable poison wnes since they are
depletable. Set=O for cladding and moderator zones since they
are none depletable.
NUCRE (57) Set=7 since 7 nuclides are present in the fuel element for
which resonance data are entered.
IDRES(J) (58) The 7 nuclides and corresponding ZAS I.D. for which
resonance data are entered are listed below.
210
RES(2,J) (60) The mean choni length, specificd by RES(2,J), was calculated
by Equatioo E. I to be 0.29cm and O.lcm for the thick plate
and thin plale reactor designs respectively.
RES(3,J) (61)
Oxygen 3.748
U235 11.500
u236 10.995
1)238 10.599
Pu239 10.200
Pu240 10.599
Pu241 10.939
Pu242 10.694
211
REs{4, u23S) = Vol%(UDI)[N 38 oJ~ + rP0p0 + ~CJp 0 ] + (1- Vol% (UOz)) Nu4<Jpzr4
Vol% (U~) N38 (E.5)
212
E.3 EPRI-CeD. Output Deecription aod Interpretation
(3) Geometry edit containing the intaval radii of the t:ach space point in the m<Xleled cell
along with its respective zone number, region number, depletion indicator and edit
indicator.
(5) Density Factors for each zone as specified by DENFRC(K,L). Note that in
this study, this input parameter has not been used.
Beginning of Calculation (Edited for Each Timestep)
(6) Homogenized Number Densities of nuclides by region.
(7) Homogenized Concentrations of nuclides for the Super Cell and the Edit Cell.
(9) Two Group High Cut Off Macroscopic Cross-Sections and kerr for lwo group
Super Cell.
213
E.4 SampJe EPRI-Cell Output File
This appendix contains two sample time steps printed with the EPRI-
Cell output file for the thick plate 97.3% enriched HEU case. The edit for
timestep 1 containa the data for the initial undepleted fuel cell calculation,
while the edit for timestep 2 contains the data for the second depletion
calculation. Also included are tbe preceding input echo back and processed
input data listings.
214
50~ RE~CTOR,CARAMEL TYPE FutL,J7PLATES,E=20.0%l~35,1.3NTY.60203,RHOU=2.077/CC.
SAD ZR4 H2'0 IAl2
FUELFUELCLADHOD CLADFUELFutLFUELCLADHOD CLADFUELFUElFUELCLADHOO CLADPOISPOISPOJS
POISPOISPOISPOISCLADHOD CLADFUELFUELFUELCLAOHOD CLAOFUELFUELFUELCLAOHOO CLAOFUEL
FUEL
FUELCLAOHOD CLADFUELCLAOMOO CtAOFUElCLAOHOO CLADPOISCLADHOO CLADFUELCLADHOD CLAD
fUHCLADHOO CL~OFUEL
UHFREE
NGEOH= 1,
Ht0?1=4.
ID= 17,
hOCliDI 11=4040, 10010,501UU,SD160,54135D,621490,6~1550,~~1570,
922354.922361,922~4,942394,942402,9424V1.9~2421,99999!,999999,
HISOHHI ll='ZR ','H ','8 ,o ,XE ,SH ,&~55',
'6157','U35 ','U36 ','Ula ','P39 ','P40 ','P41 '
'P42 ','FPI ','F?Z ,
TEHPIOI fl=63t,578,25!1,2D29J,20,7~,20,
OLDISO::O,
ISOSTPI11:121,
HnlBG=Z,
HFSB6=3,
ISOCS:1,
PUREDHI 1,11=31.0~20,1.904102,21.0~20,1.87871-3,1.9!661-3,
1.0-20,1.0-20,1.0-20.61.0-20,
PUREDHI 1,21=0.042518,
PUREOHI2,31=0.066!6102,t.DE-20,0.03343051,
PURF.DHI 1,41=31.0~20,4.64482-2.41.0-ZO,
1:'-' Z.Z6D~-2,1.D-20,6. 19342~4,61.0-20,
~ VDlFRCI2,11=0.8000,0.0,0.2000,
VOLFRCl2,21=1.0,
VOLFRCI3,31=1.0,
VOLfRCI2,41=1.0,
VOlFRCI2,51=0.80D0,0.0,0.2000,
VOlFRCI2,61=1.0,
VOlfRCI3,7J:1.D,
VOtFRCI2,!1=1.0,
VOlfRC~2.91=0.80D0,0.0,0.2000,
VOLFRCI2,101=1.0,
VOlFRCI3,11l=1.0,
VOLFRCI2,121=1.0,
VQ[ FRC I 1, 13 I= 1. O,
VOLFRCI2,141=1.0,
VOlFRCIJ,151=1.0,
VOLFRCI2, 16l=1.0,
>1)LFRCI2.17l=0.!000,0.0.0.2000,
V!OtFr.C!2,18l=1.0,
VOLFRCI3,19l=l.O,
VQLFRCI2,2DI=1.0,
VOLFRCI2,21l=0.300b,0.0,0.2000,
~FRC12,221=1.0,
'10lfP.CI3,231=1.Q,
VOlfRCI2,241=1.C,
VOLFRCI2,251=G.8000,0.C,0.2000,
OPTIOH161=I,OPTIOHI!I=1,0PTIOH1171:5,0PTtOHt24l=1,0PTIOHI251=1,
HT9=12,TI.MSTPI11=24.0,72.D,J84.0,120~.0.ZZ1~0.0,l600.0,54800.0,
PDWR=&01.01C472~.
BUCKL5=5.355661-3,
lS~EC=9,FHITYPO.O,IEDITt11=2S.1,TEHPl llc25-29l.G,
ZOHEPH 1 1=2, 1,2, 1, J ,1, 2., 1, 3, 1,2, 1, 7, 1,2, i, 3, 1,2, 1, 3, 1, 2, 1, 2,
~rKI11=0.0725,0.05755,0.26ttD,O.D5755,0.1450,0.05755,D.26990,0.05755,D.1~5D,
C.D5755,0.2699D,O.D96!~,0.D6650,D.n968D,0.26990,0.05755,0.1450,0.0575
0.2699D,0.05755,D.1~50,0.05755,0.2699D,D.05755,G.0725,
lOHECTI11=1,l0,1,30,1,3wD,1,3D,1,30,1,leD,~,
IURE:7,
IORE91 11 =922354, 9l2361, 922384, ~2l94,9ltM02, 942411,9112421,
RE911.11=10DD.D,D.29,0.43598,54.759Z5,4.52095-l,
RE911,21=1000.0,D.Z9,0.43598,3.864~09E+19,1.0E-20,
AES1l,]l21Q09.0,8.29,0.4l598,~07.73454,1.23868-4,
RE511,41=iOOD.O,D.29,0.4359&,l.864409E19,1.0E-20,
RES11,51=1000.0,0.Z9,0.4l59&,3.864't9E~19,1.0E-20,
AESI1,61=1000.D,D.29,0.43598,].8644D9E+19,1.0E-20,
RESI 1,71:100D.O,D.29,0.4359a,l.86~09E19,1.0E-2D,
&Etl
SHCJlT LIBRARIE9 CRtATtO ~ FILE!I FAST AMI THEIM. COfTAIHDIJ iHE FOLLONIHB 17 ~LIM!VTEP'ftRA'MES -
lt04tll 6l1 100101 ~s 501oe1 581 &0160/ 581 541350/ 293 6214901 29! 61H5501 I
6415701 o 922354/ 886 9223611 au 922384/ 8M 9~2394/ w 9424021 w 91t24111 186
~24211 w 99999&1 o 9999991 11
.
SPACE IHTERVAL RADII (CHt REGI OH OEPUTIOH
............
POIHT ItiER
0.0
HIDOLE
0.0
l!TER
............ R
0.02417
.........
ZOHE
I'UIIER
1
............
tUIIER
1
Jti:IICATI:Jt
.............
EDIT
ItlliCATQR
2 0.02i\17 o. Dlt311 0.07250 1 2
3 0.07250 o. 10127 0.13005 2 3 o
4 0.1300~ 0.19752 0.26500 3 4 o 1
5 0.26500 0.33248 0.39995 J 4 o
6 0.39995 o.42!73 0.45750
"5 5 o
7 0.45750 1!.43167 0.50533 6
s 0.50583 0.53000 0.55417 7
9 0.551117 0.57831 0.60250
'
5 a 1
1!l 0.60250 0.63127 1!.660)5 6 9 o
11 0.66005 0.72752 0.79500 1 10 o
to.:)
...... 12 0.7~500 0.86N 0.92995 7 10 o
....;J
13 0.92995 11.95873 0.93750 a 11 o
14 0.9!750 L01167 1.03581 9 12
15 1.035!3 1.060110 1.08~17 9 1l
16 1.03417 1.10833 1. 13250 9 14
17 1.13250 1.16127 1.19005 10 15 o
1! 1.19005 1.Z5752 1.32500 11 16 o
19 1.32500 1.392'\3 1.4591J5 11 16 o
20 1.45995 1.50855 1.55675 12 17 o
21 1.55675 1.56150 1.56625 1l 1& 1
13
22
23
1.56625
1.57575
,.57100
1.!5!050
1.57575
1.58525 13
"
20 1
~ 1.5!525 1.59000 1.59475 13 21
2.5 1.59475 1.S99!i0 1.60425 13 22
26 1.6042.5 1.60900 1.61375 13 23
Z7 1.61375 1.611150 1.6232S 13 24
~ t .62325 1.67165 1.72C05 14 25 D
29 1.7~05 1. 78753 1.!5500 15 26 o
30 1.85500 1.92248 1.93995 15 26 o
31 1. CJ!995 2.01871 2.04750 16 27 o
32 2.il475D 2.07167 2.095!!3
33 2.119583 2. 1:!000 2.1"17
"
17
28
29
~ 2. 1lt417 2.16835 2.1925!) 17 lO 1
3.5 2.19Z50 2.22125 2.~000 18 lt o
36 2.25000 2.31748 2.3!495 19 l2 o
37 2.38495 2.45243 2.51990 19 32 o 1
3ll 2.51990 2.54868 2.57745 20 3l o
39 2.577'\5 2.60162 2.62578 21 34
1:1 COtiP
HAHE GAD ZR4 H20 U02
tU: L 11
ro.
ti.IHBER 1 2 3 4
HAHE *
4040 ZIRC4
---~~****~***************~~~
1.0000000-20 4.2518000-02 0.0 1.0000000-20
10010 HYUROGEH
li! 1.000i:J000-20 0.0 6.6861030-02 1.(t!)0000D-20
50100 BOROH-10 1.0000000-20 0.0 1.0000000-20 1.000COOt-20
S0160 OXYSEH-1 1.9041000-02 0.0 3.3430510-02 4.6448200-02
1.0000000-20 a.o
t...:l 541350 XE1354 0.0 1.0000000-20
EC 621490 SH1494
1.0000000-20 0.0 0.0 1.0000000-20
641550 GD-155 1.8737100-03 0.0 0.0 1.0000000-20
64t570 G0-157 1.9866100-03 0.1) 0.0 1.0000000-20
922354 U-235S
1.0000000-20 0.0 0.0 2.260~00-02
!!!
922361 U-2369 1.0000000-20 0.0 0.0 1.0000000-20
922}84 U-23139
1.0000000-20 0.0
l:t 0.0 6. 1934210-0I't
!il
942394 PU239!\ 1.0000D00-20 0.0 0.0 1.0000000-20
942't02 PU21't0S
!f 1.0000000-20 o. o o.c 1. 0000000-20
942411 PU241S
~ 1.0000000-20 0.0 0.0 1.0000000-20
I!
942421 FU2'iZS 1.0000000-20 0.0 0.0 1.0000000-20
99999B F .P. EPI
a 1.0000000-20 0.0 0.0 1.0000000-20
999999 F.P. nlE
1.0000000-20 0.6 0.0 1.0000000-20
VOLUHE FRACTIONS
ZOHE
* NAHE FUEL CLAD HOD CLAD FUEL CUD HOO
HTRL
HUI1B HAHE "
HUHB~R 1 2 3 4 5 6 7
~************W****~********~**********************************************************************
1 GAD 0.0 0.0 0.0 0.0 0.0 0.0 D.O
2 ZR4 S.OOOOOOD-01 1.0000000+00 0.0 1.0000000+00 5.0000000-01 1.0000000+00 0.0
3 H20
0.0 0.0 1.0000000+00 0.0 0.0 0.0 1.0DOOOOD+OO
~, U02
lf
Z.OOOOOQD-01 0.0 0.0 0.0 2.0000000-01 0.0 0.0
~
* ZONE
tt NAHE CUD FUEL CLAD 1100 CLAD POIS CUJJ
Krnl tt
t..eER 8 9 10 11 12 13 14
HUH8 HAHE *
a**~~~********************************************************* ..
1 6AO "
~ 0.0 0.0 0.0 0.0 0.0 1.0000000+00 0.0
2 ZR4
lt 1.0000000+00 8.0000000-01 1. OOOOOOD+OO 0.0 1.0000000+00 0.0 1.0000000+00
3 H20
10 0.0 0.0 0.0 1.000000000 0.0 0.0 0.0
4 U02 0.0 2.0000000-01 0.0 0.0 0.0 D.O D.O
~
""""
J1 ztlHE
lf FUEl CLAD
MAME KOD CLAO CLAD HOO
tff'Rl
l'lJ'EER 15 16 17 18 19 20 21
NI..Jitm HAHE o
~----a .. ..***...****..****....
1 6AD 0.0 0.0 o. o o. o 0.0 0.0 0.0
2 ZR4
li 0.0 1.0000000+00 8.0000000-01 1.0000000+00 0.0 1.0000000+00 8.0000DOD-01
3 H20 1.0000000+00 0.0 0.0 0.0 1.0000000+00 0.0 0.0
o.o
4 U02
!11
0.0 2.0000000-01 O.G 0.0 0.0 2.0000DOD-01
f
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DEHS:nY FI.CTOR9
* ZOKE
FUEL
* KAHE FUEL CLAD ..00 CLAD CLAD t:lD
HTRL IUitER 1 2 3 4 5 6 7
*
tuB HAHE
****** ..w** ..****** .....*************~********************-.~~ow~~~~---~
6AD 1.0000000+00 1.0000rOD+OO 1.0000000+00 1.0000000+00 1.0000000+00 1.0000000+00 1.0000000+DD
2 ZR4
1.0000000+00 1.0000000+00 1.0000000+00 1.0000000+00 1.0000000+1:10 1.0000000+00 1.000000000
*
J H20 t.OCOOODD+OO 1.0000000+00 1.0000000+00 1.0000000+00 1.0000000+80 1.0000000+00 1.0000000+00
4 U02
lt 1.0000GOD+UO 1. COOOOOO+OO 1.0000000+00 1.0000000+00 1.0000000+00 1.0000000+00 1.0000000+00
~
lf.."l
.......
a .w~.. ~~~ .... ~~~~
1 6AD 1.0000000+00 1.0000000+00 1.0000000+00 1.aOOOOOD+CO 1.000000000 1.00000GO+OO 1.DOOOODD+OO
2 lR4 1.0000000+00 1.0000000+00 1.0000000+00 1.0000000+00 1.000000D+OO 1.0000000+00 1.DOOOOSO+OG
3 H20
R 1.000e30D+90 1.0000000+00 1.~000800,00 1.0000000+00 1.0000000+00 1.0000000+00 1.0000000+00
4 lMl2 1.0000000+00 1.0000000+00 1.0GDOOOD+eO 1.000000DoaO 1.COOODOD+OO 1.0GOOOOD+OO 1.0000000+10
~
.....
,.71
a ZOHE
~
---~**~*** ..************~**~**v****-~---~**..._..******-
1 6AD
li 1. 000000000 1.0000000+00 1.0000000+00 1.000000009 1.0000~DOOO 1. 00000~1JOO 1. OOOOOOD+DrJ
11'1
2 ZR4
11
1. OOOOODCOO 1.000000000 1.01)0000000 1.000000000 1.000000000 1.00000~-tOO 1. OCOODDOOO
J H20 1. OOOOOOIHOO 1.001l000D+OO 1.0000000+00 t.OOOOOOOOO 1.0000000+1}3 1. ODODDDihDO 1.000UOOOOO
4 002 1.000000000 1.000000DOO 1.000000000 1.00000CD+DD 1.DOODODDDO 1.0DODDODDO 1.DDDOOOD+GO
~
i
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c c c c
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BESIH TIMESTEP 1
REGIOH HOHOGEHIZED NUHBER OEHSITIES
REG.
"
* HAHE FUEL FUEL CLAD HOD ClAD FUEL FUEL
HL'Cl
ID.
tUeER 1 2 3 4 5 6 7
HHE
.................................................................................................... ~
40140 ZIRC4 3.4014400-02 3.4014400-02 4.2518000-02 0.0 4.2518000-02 3.4014400-02 3. 4014400-02
10010 HYDROGEN 2.0000000-21 2. 0000000-21 0.0 6.6861030-02 0.0 2.0000000-21 2.0000eD0-21
50100 BORON-10 .. 2.0000000-21 2. 00000002 1 0.0 1. ODOOODD-20 0.0 2.0000000-21 2.0000000-21
8\l16ll OXYG'EH-1 9.2896400-03 9.2896400-03 0.0 3.Yt3051D-02 0.0 9.2896400-tl3 9.2896400-03
~ 51\1350 :<EB54 * 2.0000000-21 2.0000000-21 0.0 D.D 0.0 2.0000000-21 2. 0000000-21
621490
2.0000000-21
SHl494
..
* 2.0000000-21 0.0 0.0 0.0 2.0000000-~1 2.0000000-21
641550 60-15~ 2.0000000-21 2.0000000-21 0.0 0.0 0.0 2.0000000-21 2. 0000000-21
641570 60-157 2.000000D-C!1 2.0000000-21 0.0 0.0 0.0 2.00000-21 2.0000000-21
922354 U-235S
4. 5209600-0'3 4.5209600-(13 0.0 0.0 D.O 4.5209600-03 4.5209600-03
"
922361 U-236S 2.0000000-21 2.0000000-21 0.0 0.0 0.0 2.0000000-21 2.0000000-21
922:5.84 U-2~S
!f
1. 23.!6!40-04 1.23!6MD-04 0.0 0.0 0.0 1. 2386!40-0~ 1.2386840-04
942394 P\.12394 2.0000000-21 2.0000000-21 0.0 0.0 0.0 2.0000000-21 2.0000000-21
942402 PU240S 2.0000000-21 2.0000000-21 0.0 0.0 0.0 2.0000000-21 2.0000000-21
942411 PU2419 2.DOOOOO!l-21 2.0000000-21 0.0 0.0 0.0 2. 0000000-21 2.0000000-21
9~2421 PU242S
ll
2.00001!00-21 2.0000000-21 0.0 0.0 0.0 Z.OIJODOQ0-21 2.0000QOD-21
999998 F. P. EPI
tf
2.0000000-21 2.0000000-21 0.0 0.0 0.0 2.0000000-21 2.00000~0-21
80160 OXYGEH-1
0.0 3.3430510-02 0.0 1.9041000-!)2 1. 904 UIOD-02 1. 9041000-02 1. 9041000-02
o.o
541350 XE1354 0.0 0.0 5. 07 09le2b -25 4. 7370600-Z!j 4.5891560-25 4.54m7D-25
621490 SH1494 0.0 0.0 0.0 2.5237200-25 2. 2692730-25 2.1852090-25 2.16139~-25
641550 G0-15.S 0.0 0.0 0.0 1.8736920-03 1.8757390-03 1.8759690-03 1.1760200-Gl
~ 1. 980886U- n
641570 60-157 0.0 0.0 0.0 1. 971~10-03 1. 9819620-D:! 1. 9322010-03
922354 U-2359 0.0 0.0 0.0 9.9953760-21 9.995703D-21 9. 9957850-21 9.9953060-21
922361 U-2369 0.0 0.0 0.0 9.9983240-21 9.99827~-21 9.9912620-21 9.9912590-21
922~4 U-2389 0.0 0.0 0.0 9.9917G8D-21 9.9977090-21 9.9977100-21 9.9977100-21
9'\2394 PU239~ ~
0.0 0.0 0.0 9.9874870-21 9.9391030-21 9.9896970-21 9.9893690-21
942402 PU240S .
li
0.0 0.0 0.0 9.9479540-21 9.9476110-21 9.74560-21 9.M7411D-21
942.'t 11 PU2419 0.0 0.0 0.0 1.001t469C-20 1. 0045730-20 1.0M606D-20 1.0046160-20
942421 PU2429 ..
if
0.0 0.0 !LO 9.9946740-21 9. 9943450-21 9.9942350-21 9.994204D-2t
999998 F.P. EPI
lf 0.0 0.0 D.O 6.0865780-05 2.7224380-05 2.3434690-05 2.2592280-05
;J
999999 F.P. THE .. O.D 0.0 0.0 7.9603250-05 3.4209990-05 2.9094910-05 2. 7958230-05
REG
*
HAHE POIS POIS POIS CLAD til) CLAD FUEL
tU: L 11 ti.I'SER 22 21 24 25 26 27 28
ID. HA.HE *
111111*~~-~. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
4MO ZIRC4 1.0000000-20 1.0000000-20 1.DOOOOOD-20 lt.2518DDD-02 0.0 4.2515000-02 3.4014400-02
10010 HYDROGEH l.OODOODD-20 1.000000D-20 1.0000DOD-20 0.0 6.6861030-02 0.0 2. 000000021
50100 BOROH-10 9.982J5lD-21 9.9818450-21 9 9798050-21
o G.O 1.0000000-20 0.0 1.99~1740-21
~0160 OXYGEH-1 1.9041000-02 1.9041000-02 1.904100D-D2 0.0 3.3430510-02 0.0 9.2396400-03
541350 XE1l54
111
4.5891590-25 4.7370720-25 5.0709570-25 D.O 0.0 G.O ]. 72442tD-08
621490 Stt1494 2. 1852110-25 2.2692800-25 2. 5257290-25 O.D 0.0 0.0 1. 9703910-08
641550 60-155 1.8759690-03 1.8757390-03 1.87~920-03 O.D 0.0 0.0 3.6566420-13
EZ 641570 60-157 1. 9819620-03 1. 9SDM6D-03 1.9713470-03 0.0 0.0 0.0 5.1251380-11
~
922354 U-2359 9.9957340-21 9.9957030-21 9.9953760-21 D.D 0.0 0.0 4.5182030-03
922361 U-2369
9.9982620-21 9.9982750-21 9.99832itD-2' O.D 0.0 0.0 6.6511750-07
9223M U-238S 9.9977100-21 9.9977090-21 9.9977080-21 0.0 0.0 0.0 1. 2383990-04
942394 PU239~ 9.9896970-21 9.9891030-21 9.9874870-21 0.0 0.0 0.0 2 .8024730-DI
942402 PU240S 9.9474560-21 9.9476110-21 9.9479530-21 0.0 0.0 0.0 1. 0588250-11
942411 PU241S 1.0046070-20 1. 0045730-20 1.00"690-20 0.0 0.0 0.0 1. 979011D- 14
942421 PU2~2S 9.9942350-21 9.9943450-21 9.99467't0-21 0.0 0.0 O.D 1.9991630-21
999998 F.P. EPI 2.3434710-05 2.7224460-05 6.0866030-05 0.0 O.D ,,0 :5.605.5680-05
999999 F.P. Til E 2.9094930-05 3.4210090-05 7.9603580-05 0.0 0.0 0.0 2.6896530-04
lf
~EG .
~ HAHE FUEl FUEL CLAD HOD CLAD FUEL FUEL
~1JCL tf.I'IBER 29 30 31 32 33 ~ 35
ID. HAHE
~-**** ..v..***e...R*W...--. ......w***-.....--....
4040 ZIRC4
11 3.4014400-02 3.4014400-02 4.2518000-02 0.0 4.2518000-02 3.4014400-02 3.401"00-02
10010 HVDROGEH
2.0000000-21 2.00000C!J-21 0.0 6.6861030-02 0.0 2.0000000-21 2.0000000-21
50101) SORON-10 1. 9942q00-21 1.9939850-21 0.0 1.0000000-20 0.0 1. 9936570-21 1. 9938020-21
80160 OXY6H'-1 9.2!961\0D-03 9.28961'100-03 CI.O 3.3430510-02 0.0 9.28964DD-03 9.2396400-03
541350 XE1354
I!
3.701330D-08 3. 7621690-08 0.0 0.0 0.0 3.8203CBD-08 3. 7837780-03
621490 SH1494
ti
1.9504D9o-oa 2. 0249470-08 0.0 G.O 0.0 2.117631~-oa 2.0746820-oa
641550 Ei0-155 3.6194060-13 3.7604810-13 0.0 0.0 o.a 3.9379160-13 3.8568500-13
~
11
641570 Ei0-157 v 5.0n718D-11 5. 2656450-11 0.0 o.a 0.0 5.5058690-11 5.3967050-11
922354 U-235S
~
4.51&2290-03 4.5181320-03 0.0 0.0 11.8 4.5~0110-03 4.5180660-03
922361 U-2365 il 6.6127800-07 6.7603650-07 0.0 G.D 0.8 6.9W25D-07 6 .86ltlt 11-07
o.a
92238tt U-2389 1.2383990-04 1.2383990-04 0.0 0.0 1. 2383990-M 1.2383990-0~
942394 PU2394
2.8022060-08 2.8032290-08 0.0 0.0 0.0
~
2.3045330-08 2.8039480-0S
Cll4~02 PU24DS 1.047011D-11 1.03930~-11 0.0 0.0 0.0 1.1451090-11 1.121"50-11
942411 PU241S 1.9322670-iif 2.0312330-14 0.0 0.0 0.0 2.124887D-14 2.0.563040-14
942421 PU242S
R 1.4i991550-21 1. 9991390-2, ll.D 0.0 a.o ~.9992360-21 1.9992180-21
999998 F. P. EPI
3.5686800-05 3.7052970-05 0.0 0.0 0.0 3.8137310-05 3.3034040-05
999999 F .P. THE
lli 2.6621190-0t\ 2. 76641SD-O~ D.O O.D 0.0 2.8975130-Cit 2.8375220-0it
~ REG.
~ FUEL CLAD t10D CLAD fUEL ~un
ti.JCL
ID. HAHE
tutBER 36 37 38 39 40 41
...... ~ .............................*****.............................................................
4040 ZIRC4 3.4014400-02 4.2518000-02 0.0 4.2518000~02 3.~014400-02 3.401"00-02
10010 HYDROGEH 11 2.000000D-Z1 0.0 6.6861030-02 0.0 2.0000000-21 2.0000000-21
50100 BOROH-10 1.9935860-21 D.O 1.00D0000-20 0.0 1. 993't50D-21 1. 9936640-21
80160 OXYSEH-1
.. 9.2896400-0l 0.0 l."'3051D-Q2 0.0 9.28961t00-0l 9.2896400-03
541350 XE1354 3.8325180-08 0.0 0.0 0.0 3.8573580-08 3 .8Ga372D-08
o.o
621490 SH149~ 2. 1378820-08 0.0 0.0 2. 1767010-0& 2. 1136890-06
641550 60-155 3.9766320-13 0.0 0.0 0.0 4. 0508310-13 3.9314990-13
~ 641570 60-157 5.5580210-11 0.0 0.0 0.0 5.6580350-11 5.4976170-11
922354 U-2359
4.517984D~D3 0.0 0.0 0.0 't.517933D-D3 4.5180150-03
922361 U-236S 6.9.!93590-117 0.0 0.0 0.0 7. 067636D-07 6.9434050-07
o.e
922lM U-238S , .2~~~?90-04 G.O 0.0 1. 2383990-04 1. 2383990-04
942394 PU2394
2.80431SD-08 0.0 0.0 0.0 2.8053630-0S 2.8044990-08
942402 PU2409 1.1561670-11 0.0 0.0 0.0 1.1785720-11 1.1443300-11
942411 F\12419
J:
2. 1~43340-1~ 0.0 0.0 ~.0 2.1896110-14 2. 0977250-14
942421 PU242S 1.9992463-21 0.0 G.O 0.0 1.fl926SIJ-21 1."92370-21
99999& F .P. EPI
li
3. 9220540-05 0.0 0.0 0.0 3.'1954910-05 3.8772350-05
999'!199 F.P. THE 2.926f49D-04 0.0 0.0 0.0 2.9310170-04 2.8926900-04
ZOHE HOHOGEHIZED HUHBER DEH91TIE9
11 ztM
*
HAHE FUEL CUD fG) CLAD FUEL CLAD JGJ
tiJCl e N.leER 1 2 3 4 5 6 7
ID. HAHE tt
a....w~..._ ... N....w..ww..wM .............masK
~MO ZIRC~
3.4014400-02 ,.,251&000-02 G.O 4.2511000-02 3.4014400-02 4.2518010-12 G.t
c.o
10010 HVDROGEH 2.0060000-21 6.6861030-02 0.0 2.0000000-21 0.1 6.6861030-02
50100 BOROH-10
R 1. 9935570-21 0.0 1.0000000-20 0.0 1. 993682D-21 0.0 1. 0080000-20
80160 OXYSEN-1
!!i 9.2896400-0! o.o l.3430.5,D-02 0.0 9.2396,.00-0l O.D 3. 3430510-02
5tt1350 XE1354 3.8329870-08 0.0 0.0 0.0 3.1121970-01 0.0 D~O
~ 621490 SH1494
Q 2. 1452280-08 o.a 0.0 0.0 2.1100.58D-D8 O.D D.O
a.o
641550 60-155 3.9911980-13 0.0 O.G 3. 923761tD-U 0.0 0.0
641570 00-157 5.577S97D-11 0.0 0.0 0.0 5.W8260-11 8.0 1.0
922354 U-2359
11 4.5179740-03 e.o 0.0 0.0 4.51SC20D-03 O.D 0.0
~
4040 ZIRC4
~.2518000-02 3.4014400-02 4.2518000-02 0.0 4.2518000-02 1.0000000-20 4.2518000-02
*
o.o
10010 HYDROGEH
111
O.tl 2.0000000-21 0.0 6.6861030-02 1.0000000-ZO 0.0
50100 BORmf-10 0.0 1. 9941330-21 0.0 1.0000000-20 0.0 9.9814990-21 0.0
aot60 OXYSEH-1 * 0.0 9.2896400-0] 0.0 3.Yt3G51D-02 0.0 I. 90411011-02 D.D
o.e
541350 XE1354 0.0 3. 7292t90- 08 0.0 0.0 0.6 4.7627930-25
621490 SH1494
0.0 1. 9819050-08 0.0 0.0 o.o 2.30254SD-Z5 D.l
o.o o.o
641550 EiG-155 o. o 3.6788120-13 0.0 0.0 1.8752600-03
~ S41570 60-157 0.0 5.1551290-1 t 0.0 O.IJ 0.0 j. 9786560-03 O.D
922354 U-235S 0.0 4.5181880-03 0.0 0.8 0.1 9.M56W-21 O.D
922361 U-2J6S 0.0 6.6747420-07 0.0 0.0 0.0 9.991ZalD-21 0.0
o.o o.o
922384 U-Z38S 0.0 1. 2383990-04 0.0 0.0 9.9977090-21
942394 F\.12394 0.0 2.8026270-08 0.0 0.0 0.0 9.91&9210-21 0.0
o.a o.a
942402 PU240S
0.0 1.0650350-11 0.0 9.9476360-21 0.0
9ft2411 PI.J241S D.D 1.MOSUD-14 0.0 0.0 0.0 I. OK559D-20 a.e
o.o
942421 PU242S 0.0 1.9991690-21 0.0 0.0 9.9M381D-21 0.0
99999S F.P. EPI
1!1 0.0 3.6274950-05 0.0 0.0 o.o 3.5091760-05 0.0
999999 F.P. THE
'li 0.0 2.7060ft80-0~ 0.0 0.0 0.0 ~.48250110-05 0.0
g
~ Z\M:
!I
ti.JCL
5
HAHE HOO CLAD FUEL CLAD PQI CUD
ID. twtE
tueER 15 16 17 18 19 20 21
. . ~.-~.._ . . . . ~ . . . . . . . . . . . . . ~..._._ N..._. . . . . . . . . . . . .._ . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
I!
4040 ZIRC4 0.0 lt.25180DD-02 3.4014400-02 4.2513000-02 0.0 4.2518000-02 3 .40 11tlt00-02
c.c
10010 HVDROGEH e 6.6861030-02 0.0 2.0000000-21 0.0 6.6861030-02 2.000DO!l0-21
5011)0 BOR00-10 ~.OOOOOOD-20 0.0 1. 994 13:50-21 0.0 1.0000000-20 o. o 1. 993682D-21
80160 OXYEiEH-1
., 3.34305111-02 0.0 9.2896400-03 0.0 3.3430510-02 0.0 9.2896400-03
o.c
541350 XE13S4 0.0 0.0 3.7293070-08 0.0 0.1 3.8 122C10-DI
621490 SH1494
0.0 O.G 1. 9819160-03 0.0 G.~ D.D 2.1100610-Da
~41550 GD-155 0.0 0.0 3.67&8430-13 0.0 0.0 0.0 3.9237990-13
e.o
641570 60-157 0.0 0.0 5.1551670-11 0.0 6.0 5.48686!5D-11
u.o
922J~ U-2359 0.0 4.5181880-03 0.0 0.0 0.0 4. 5180201HI:S
922361 U-2J6S 0.0 0.0 6.6747730-07 0.0 0.0 0.0 6.9341320-07
9223.84 U-2389 0.0 0.0 1.2383990-0~ 0.0 0.0 0.0 1.2383HD-04
942:594 PU2394
Q 0.0 0.0 2.8026360-08 0.0 c.o 0,0 2.1044330-Da
942402 PIJ2lt0S 0.0 0.0 1.0650470-11 0.0 o.~ 0.0 1.11t0907D-11
942411 PU241S 0.0 O.D 1. 9!0351W-11t 0.0 0.0 0.0 2. 10S501D-14
942421 PU2429 0.0 0.0 , . 9991690-21 0.0 0.0 0.0 1.9992330-21
999998 F .P. EPI
M
0.0 0.0 3.6275150-05 0.0 0.0 0.1 3.8697300-05
999999 F.P. THE
11
0.0 0.0 2.7060630-0~ 0.0 0.0 0.@ 2.8170610-04
lll ltH
tWfE
NUCL
ID. HAHE
tOe ER 22 23 ~ 25
40~0 ZIRC4
4.2518000-02 0.0 4.2518COD-IJ2 3.4014400-02
10010 HYDROGEH 0.0 6.6861030-02 D.O 2.0000000-21
50100 BOROH-10 "'a 0.0 1.0000000-20 0.0 1. 9935570-2 i
80160 OXYSEH-1 0.0 3.3430510-02 n.o 9.2896400-0l
.54B50 XE1354 0.0 0.0 0.0 3.8328650-0S
o.c
621490 SH1494 ti.O 0.0 2. 145 '95D-M
641550 GD-155
' 0.0 0.0 0.0 3. 9911650-13
~
641570 60-157 0.0 0.0 0.0 5. 5778260-11
922354 U-2359 0.0 0.0 0.0 4.5179740-03
922361 U-2:56S *I' 0.0 0.0 0.0 7 '055210-07
922384 U-238S
11
0.0 0.0 0.0 1.2383990-114
942394 PU2394 ~ 0.0 0.0 0.0 2.8049310-03
lf
9ft2402 PU24GS l1.0 0.0 0.0 1.1614510-11
942411 PU241S
I&
0.0 0.0 0.0 2. 143b680-1ft
942421 PU2429 0.0 0.0 0.0 1.9992510-21
999998 ~ .P. EPI
111 o. o 0.0 0.0 3.9363630-05
o.c
999999 F.P. lHE
~
0.0 0.0 2.9363530-04
~liDE HOHOGEHJlED CONCEHTRATJOHS
GRruP OIFF. COU. TRAHSRJRT SCA TT'EJ! IH& RE'IJVAL P-1 SCATTER:tH6 P-1 REKJVAL
HORH10-1DOO: TOTAL PONER : 6.0101050002 IWATT~) J'AST FRJCTIDH =0.,101) ntERMAL FRACTUif =ll. 58987
TlttE FOR SAtt-TllERmS FLUX CALC\A.ATIOH
HUttiDE-ZilfCit
GIIP ABSOOPTIOH FISSIIJ4 sunEJtJH& TOTll. NJ-FISSIOH 11l AHSF'(JI f RHfl\IAL H-2-H KAPPA FISSIOH IR f
1 0.0 0.0 0\.975-75000 4.97575000 0.11 4.4~42000 ~.415600-01 7 .!45700-05 D.O 4. ~!71[1-02
2 1. 065570-03 o.o a. o&l65DlJO 11.0&1\72::100 0.0 7 .179J8DOD 2 .ZOl96D-D2 0.0 D.D J.5J994D-OZ
l 1. 538140- o' 0.0 6.7l6&2DIIO 6.11')06~DOO o.o 6.8557,0+01 1.15:M7D-02 0.0 0.0 1. !434ZD 02
4.170080-02 0.0 6.]1<\alODII 6.l~5lll~oa o.o 6 .309700110 1.l86HI0-01 0.0 0.0 1.27.3750-01
"'!5 a. 12oso-oz 0.0 6.06000Dtll0 6.1't1J8Dt00 D.D 6. 0938.3GOD O.D 0.11 D.D 0.0
HUCLIDE-HYDR06EH
6RP ABSOIIPTIOH FISSic.l !!ICATTEJIJMi TOTAl 111- FI 'JS lctl TRAHSPORT IIEtCJVAL H-2-H kAPPA F I!35ID'i IRT
1 l.tti7450-D5
2 1.45Sl7D-O'i
1.0
C.l
3.M213Dil 3.04216011
1. 189170&1~ I. 109t9Dt1 1. 706 71D DI 1.66l750oDI 0.0 D.O 2.03414010
3 7.702320-13 c.o 2.1ll54011 Z.t34lJDI1 t.D 3.291660611 2. 13329000
5.99220000 1.884700011
O.D
I.D
D.l
D.D
2. 13-'tlJCDO
2.H353DOD
4 5. 19 1it2D--OZ UI a. tlii6':50DD 1.99057DDt 1.1 9.21l60DDO a.9Ja6500D 0.0 O.D 1. 7632600 1
5 L51014D-ii1 0.0 2.1071011 2. 15311001 I.D 1.89!7MD1 11.11 0.0 0.!1 0.11
HUtliDE-BORDH-10
SRP A35a'P1IOH FIS5ICI4 ~TTDIIIII TOTAL tiJ-FISSIOH TWAHSf'G'T IIEtCJVAL H-2-H UPPA FJSSII> illf
1 2.'122760-!1 fi.t t.a1557DOO 2.117MODI 0.1 1 .75951000 1.102210-01 iJ.I 0.0 1 . .369450-01
~ Z
l
4
2.118997000
a.36959081
5.97326002
0.11
0.0
0.0
2.99038000
2.191110+00
2.024950+00
5.11&035000
9.11MDDD1
5.99]511.102
11.1
t.D
4.68900000
1.88259011
5.a~15BDII2
4.26\510-02
3.35.3620-02
0.1
o.o
D.l
1. 1271iXl-ot
~. 9455l!Hl2
0.1 3.818470-01 1.11 D.O 3.5G8950-0t
5 1.67382DOl 0.0 2. 13168000 1.67595003 O.D 1 .34016003 0.0 O.D 0.0 11.0
HUtl!DE-OXYGEH-1
&RP ~PTlc.l
1 a. 0649!10-DJ
2 11.0
J 6. 170 110-M
4 2.a 151ao-o5
0.0
~
11.0
0.0
..
FI5'31DH SCATTEIUH8
2.476.JOD+OI
3. 9D776U+iJI
:S.63N1DOl
3.80D64D+08
TOTAL
2.'\1431DDU
3.9071~01
J.68&&2DOO
3.!1ti066DDO
~FI'JSIIt
0.0
D.l
1.0
!1. o
TRAHP'ORT
2.11667011
l.571S67Dt00
3.54D~OO
3.64081t0lll
ltEtCVAL
:S. 11D77D-11
4.723190-12
3.16DODD-12
4.596760-01
H-2-H
o,o
1.0
1.1
1.0
t:'"""A FISSICJH
o.e
1.0
I. O
0.1
UIT
1. 191010-11
9.4526~-12
5.57&890-112
4. 224160-0 I
5 7. 94D9D-05 0.11 3.995710+00 .3.99579000 11.0 3.81~23000 0.11 0.0 11.0 O.D
i:t I!IE-$W;9:0
I!IIIP
DSORPT IOH FI!I'SIOH SCATTDIIHS TOTAL tti-FIS910H Tl.t.HSPOIIT IIIDIWAL lt-2-H Kii'PA Fl991~ IRT
1 5 . 2:>860-;)2 0.0
z 9.2628~-01 0.0
6.70438000 i.76Z610til
. 311UDGO 1. ll2550DG 1. 150270-02 O.G 3. 6Z252D-12
l '. 7023800 1 0.0
9.00i821DOD
6. 27303lltllt
9.97-\5CODI
1. ~75-WJ Dl
D.lt
9.l129aDDD
1. 57792DD2
2.71122J1-DZ
1.249850-02
0.0
!1.11
O.D
o.c
2."3020-12
1.t5&57D-Ii1
4 1.U925tJ03 0.0 3.~4111DD1 '. 92'390003 l!l.t 1.6060!002 4.6770~0-01 1.0 0.0 4. Z979l0-D I
5 1. 901'67004 0.0 1.59816002 1. 91665:104 11. o 1. 74M7Db3 D.D 0.0 0.0 0.0
1-IUtllOE-G0-15~
,
&RP ASstWtPT I ()I
2
2.228690-01
1.78424000
FJSSIC!tt
e.o
0.0
!ICA'ITEIIINB
6.521380taD
8.~57720011
TOTM.
6.744250110
1. 02tt2'0D 01
ttJ-FlSSI()I
0.0
a.o
TliAHSPORl'
4.~~37Det
8.392970011
RlPJVAl
1.63637080
1.869350-0Z
H-2-H
0.0
0.0
KAPPA FISSIDH
0.0
0.0
lRT
3.382070-02
2. 193 1"0-02
l 1.304~002 0.11 1. t97260trt1 1.423960112 tLO 1. 378731112 3.539650-0't 0.0 a.o 1.940360-02
4 3. 146"'0+CU 11.0 D.l 3. 1~41001 1.11 1. 76472110 1 0.0 0.0 0.0 D.O
5 5.6~610002 0.0 0.6 5.64610002 0.0 l. Yt251DII2 0.0 0.0 0.0 0.0
~LIOE-60-157
IIIIP A9S(JIPTIIJ'I FISSUJH !CATTtiUtll TOTAL NJ- FIS31114 TRAH9PORJ R[PIOYAL H-2-H I(APPA FISSICtl IRT
1 7 .501!J2D-01
2 3.943700110
3 S.~31GDOI
O.D
0.!1
0.0
6.51893000
S.31MlDDD
1.50898001
7.26911001
1 .226751lOt
9.99208011
o.e
0.0
4.96166000
1.0277000 ~
9.866'tZDD1
1. 635710 DO
1. 8292.50-02
5.702810-03
0.0
e.o
O.D
0.0
11.0
11. o
3.337740-DZ
2.129650-02
2.414410-0Z
1.0 1. 303930. B2
4 1. 303930>0Z
5 2.46319003
0.0
O.D 11.1 2.46J19DDl
lU
D.ll
7 .283640111
,.50179003
0.1
o.a
D.D
e.o
0.0
0.0
0.0
IU:LIOE-U-:!355
1111 P A89(J! I'TICJI Fl~JCJI !ltAT'TtRJNB TOTAL ttJ-FlSSI~ TRAHSPORT REtiOYAL H-2-f4 KAPPA FI~IOH !RT
:so
~
1 1. !36000 1.23640000 5.88864000 7. 190011000 ].35488000 ~.718~00 7.536700-11 8. 106350-03 3.946190-11 2.1115870-02
2 2.09ZS4DDII 1.632760+00 8.82115000 1.09137DD1 ].991650+00 9.2tt6'+60DO 1. 111440-02 0.1 5.N91D-11 1.50MSU-12
3 J. 15~SZD01 2.02628Dll1 1.217""D+D1 4.37697DD1 4.90123001 4.32950001 1.52M50-i:l3 o.o 6. 66JDJI1111 1.~00-0Z
4 5.367~!11 ~-~5703001 1. 185480 OI 6.55302001 1. 10225DtOZ 5.262S1DDt 1.114570-111 O.G t .rt5986D-D9 9.323320-02
5 2.3B96DD2 1. 95555002 1. 11i384001 2.42834002 4.73008002 1.87513002 0.0 11.0 6.353610-09 0.0
tU:LTDE -U-2369
G!P .I.SSORPT ICJI FI"IOit !IUTTERIHB TOTAL ttJ- FISSIOH TRAMSPIJII r lltiHAL lf-~-M KAPPA FI9SI!Ji Ptr
1 8. 712'HD-0 1 7. 16aG7D-01 6.68lG2DDO 7 . .55427000 1. 95!5641101 5.172570111 1. !118300 tO 7.900070-113 2.266650-11 2.278,311-12
z 4.579140-01 7.1S4432D-Dl 1.M6260n 1. 14205001 1. 939690-112 9.a81MODD 1.444280-R
2.498010-13 1.868Wl-OZ
l 3..~1\60001 0.0 2.ltJ167DOt 5.81li21'0D1 a.o 5.737000+01 6 .24712D-03 1.1 o.a 2.590370-02
0.0 0.0
4 1.0G9ttZDDD
5 , .59.536000
0.0
0.0
a.69l37DOi
6.99~92DOO
9.70329GOO
8.58978000 ~.0
9.67802DDO
8.51JOlDDD
7.409000-02
1.0 1.0
e.o
6.!SM1t50-0Z
0.0
tJCLIDE-U-23115
6RP ABSORPH~ FISSION SCATTEIIIINS TOTAL 'i.I-FISSICII TlbHSPORT REPIJVAl H2H KAF'f'A ;: I SSIOH IRJ
I ~-~il5'40-01 3.61MlD-01 6. 906630+00 7 .31.."680110 1. D095lUI ~.;~CD 1.31621000 1.622111J-02 1. 16Z050-11 2. 3l458D-OZ
z Z.58liHD-01 l.63&6D-04 1.W910t01 1. 10971Qt01 8.797391HM 9.l089lDDO 1.462070-DZ l.t 1. 17~680-14 1. 831910-0Z
J Z.7U'i'24001 7.M555D-C5 2.9351"'+01 5.6"'t4DD1 1.!SZ9150-D4 5.54M0011 6. 113&70-03 11.0 2.599Z2D-15 l. 1001t7D-OZ
~ 5.11!5750-111 l. 962alD-08 8.4~16000 8.9627%000 9. 1~1760-08 1.9,726DID 7. 144180-112 0.0 1.27~000-13 6.565090-02
5 1. OS45DDOD 0.0 e. IS704DOO 9.2115o'!D+OD 11.0 9.18150000 0.11 0.0 0.0 0.0
tu:LIOE-PU239'
GJ:P ABSORPTICtl FlSSI~ SUTTlRlH8 fDTAl ttJ-FIS!IOH TRA~m'URT REPIJVAL H-2-H KAPPA FISSIOH DIT
1 1. 856570110 1.8'"720~1 5.47671DOcl 7 .ln27DOO 5.91101011 5 . 02t\42ll DO I.Z0871D-11 3. 380850-113 6.U~t~a-11 1.143500-02
2 1.9H~DDO 1.62'1156000 8.66829001 1. 061\1600 1 4-72M!iD+OD 9.0049lDU 1. 6749110-0Z 0.1 5.3.56300-11 1 . 458900-02
3 4. 1!24700, 2. 361\0ZDO 1 1.31:53:~~01 5. -\9!58000 1 6 .7926000 1 5.428Z2D01 6.M7~2D-D3 c.o 8. 00l57D-10 1. 3& 1490-02
4 5. ztl~99ilG 1 3.1t69M01 9.5.5619000 6.211,.0011 t.HI7lD02 5.31947DDt 8.141700-02 0.0 1.~383009 7 .l!I986D02
s 1. 111160+0] .a~.w~~cz 7.M7!w.)CO 1. 111!1850+03 1.97062D+IIl 5.41J375oD2 11.0 0.0 2. 2!99,.003 0.0
N'XLIDEPU24G9
~p ABSORPTIOH FISSI~ SUTTERIHII TOTAL 1.1 FI SSHif ntAHSPORJ REIIJVAI.. H-2-H klPPA FISSJOH IR f
1 L65l!lDDD 1. 59299000 !I.W440+~11 7.20027D+OQ !1. 111221! DO 4. 9~37oOD 7.6~41001 t.l67MDOl 5. 155230-11 1 .!5920002
2 6.5le'f60-01 l::.6318!.001 1.02'\1lD+01 1. 0895tD+01 7.760MD-01 9.0158.50+00 1.43172002 11.0 8.591160-12 L 7161t6D-02
3 1.8111l2DDt 2.123700-01 2.51U10+11 4.3.YtD3itGt 6. 109180-01 4.l21tOZD+111 2.021580-02 11.0 7. ll2l50-12 2. 6lii21D-G2
4 6 .lt4095003 ~ 2Z9Z8D 1111 3.05'110001 6 .47176D+O:S 3. 52779001 3.66291002 2.582590-01 0.1 3.9951511-11 2.373260-01
5 1.%0:59002 2.87~720-0l 2.479170+111 1.70531DC2 1.2"4140-02 1.6 1678002 l.t 0.0 9.4913]ll-13 0.0
HUCliDE-~IS
~p lli!SORPTIO"tf FI,IOH !ICATTOINI TOTAL 161-FIS91Cif T1t1H91'0111T RE110'ill H-2-H KAPf"' FISSIDii IIIJ
t t. 74606000 1.654550+11 5.17206Ct 7.618 1211+01 5.3947~01 ~-9~+11 1.~717~-11 2. 2728211-02 !1.50047011 1.960250-02
2 2.456550+00 l. 101~CI 9.513590+10 1. 1t701Dtlt ~.22371001 'L54&11\D+Dt 1.2015211-R 0.1 7 .041780-U 1.5&79~-02
3 6.6~+01 5.43546a+Of 1. 25408011 7.f0ZJ7DI1 ,_ 59315Dt2 7.77967001 6.031900-03 0.1 I. 870850-09 1.3118260-12
4
5
3.58!Yta+Oi
6. 719l01J02
3.1.1&866001 1.4884'1011 4.51211111 9.15686001 4.39718001 7. 918710-02
,. .9197'NJ02 7.6330~+00 6 .85,.30+12 1.44Z. 111+03 l.M662DD2 1.0
0.1
.Olt:JSG-H 7.276910-02
1.6699~-oa 0.0
tU:liGE-PU2429
6RP MSGIPTIOH FI !!I IOH ICAnEJn. TOTAL MJ-FJUJCit nt....,..T ltfiiJVAL tt-2-N F.IPI'I FISSII:Jf nn
! 1 L510't6DOO
2 4. 1711~1-01
1.471671)+00 5.t.5110D+O!I
1.6889!!1-11 1.076280+01
7. 16155011 4.645SBDII
1. 117WID01 4.879760-11
~.69581001 6.590170-01 5.19ot90-D5 4.7597211-11
9. 13559010 1. 7291180-12 1.1 5 . .508200-12
o.e
1.8173!ICI-02
!.71775012
3 9.ZV757D01
4 f.2Zl58DOO
0.0
o.e
3.357ot3Do01
4.4591Stt+Gt
1. 265530112
1.3632a011
1.21510002 2.9t939D-t3
1.21478001 3.7113450-0Z . lt.l
3 "i55:5D-02
3.403260-02
5 6.45577000 lJ.D 3.5&717D~oo 1.004291101 D.l 9. 90!180 to 0.0 a.o 1.0 0.0
HUCllDE-f.P. EPI
&aP .taSORFT lt!t FI!'JIN SCAn~Il-16 TOlA!. ..,_ nss IOH TUHSPC!RT JIEMIJVAL tt-2-H UPPA FISSI~ IIIT
t
z a.o
lJ.O 0.1
0.0
O.t
11.1
t.O
e.o
D.l o.e 0.1
1.1
1.1
1.1
1.1
11.0
0.1
HUtliOE-F.P. THE
&RP
t
2
l
AB'lCJ'PTtOH
o.a
0.0
ti.O
FISSICIH
0.0
a.o
B.D
SCAmlfJNS
1.0
o.a
CI.O
..,
TOTAL
1.0
0.0
tJ-FIS!IICtl
0,,
1.1
T11D!Sf'OR T
0.0
Jlt1'GV1ll
J.O
1.0
H-2-M
lt.a
1.1
ICAJIPA. FISSIOH
t.l
o.e
0.1
1.0
D.D
(i.D
I'IT
SRil I.BSORPTI~ FISSICtt ICATIERM TOTAL tll-FISSICIH lltAHSPORT REJIJYAL H-2-N KAPPA FISSIOH IRT
1 1. 552040-ll 1.21462D-13 2.'151lD-11 2.5110660-11 l.W5.2Dt3 1.!321190-11 7. 16~090-02 1.02288D-05 4.101030-14 7.2414211-02
2 2.42248!>-U 1.6&2950-ll i.D95510-11 i\.1191JII-11 4.114370-0l 3.l28801Ht1 7.397100-02 1.11 5.4118221H4 7.517570-02
l 4.50167D-D2 2.188560-tz 9.~77DII 9.45'i940-fll 5.051&SD-02 4.5258JD-01 6.~H817D-02 D.O 6.86784D-1l 8.5729211-Gl
6.451l31HI:! 4.697itD-G2 5.149840-11 5.694971-111 1.136140-11 5.5927~-01 5.810190-01 O.D 1.S047ft0-12 6.127300-01
"
!l 1.696650-01 2.111!5WI-111 9. 29l24iH11 1.2919901111 4.57547tHH 1. 111091008 II.C o.c 6.~910-12 11.0
k-EFF. = 1.1Xt~O
K-INf. : 1.29359
PHJ
AS!ImPTt~ IIJ-FIS910f DIFFU9IOH Cllf!T ~A Fl!I'JIOH AYI.CELl vtlOClTY
~ 8.9}g1711D-01 1.177791000 1.4745910-01 1.582052D-11 2.415749000
SlH1.ARY TAB!.E
I HlMHALilrD TO 0HE HEUTROH LOSS I
FRACT!OHAL
HUtliDE DENSITYI K&/1. I ABSORPTIOHS FlliSIOHS PROOUCTIOHS POWER
ltOitO ZIRC4 2.73218000 2.213670-02 i). o 2.520640-05 0.0
100 10 HYORCGEH 5.697900-02 8.964410-0l 0.0 G.O 0.0
50100 Bc.(lf-10 0.0 t. 705360-17 0.0 o.o o...
80160 OXY&EH-1 5.191200-01 1.1tC6480-03 0.0 o.o 11.0
54 1350 XE 1354 0.0 ft. 571t36D -16 0.0 o.o a.o
6211t90 Stt1494 o.o 1.553700-17 0.0 1.362670-22 ii.O
641550 G0-155 1.010610-0~ 6.312730-02 0.0 0.0 0.0
6~1570 60-137 1. 08252D -02 1.457!90-01 0.0 o.o o.o
92235&\ U-235S 4.02272D-01 5.748720-01 lt.l!S3Z6D-01 1. 064200+00 9.997950-0t
922361 U-236S 0.0 1.707050-19 ft.3Cl20D-21 1.181920-20 9.533600-21
9223M U-2383 1.116270-02 5.688890-03 9. 11444D-05 2.623790-04 2.050J80-04
9lt2391t M394 0.1 1. 077160-18 6. 6~13~0-19 1. 913070-18 1 . 556150-11
94~02 ~09 0.0 3.271100-18 1.2.-:17/20-20 4.060610-20 2.9~30-20
M~11 f!U2lt1S 0.0 a. 661~50-19 6.64l750-19 1.9SZ09D-14 , . 586930-18
94~21 ~2S 0.0 4.620390-19 9.952490-21 3. 11561P-20 2.257l30-20
~ 999998 F .P. EPI
999999 F. P. lHE
o.o
0.0
5.207180-21
2.230970-22
0.0
0.0
0.0
0.0
0.0
O.fJ
TOTAl TOTAL TOTAl TOTAL
.IBSORPTIIIG FISSIDHS PROOUCli<If.l POWER
1.220350-01 4.314170-01 1. 06ltl9D~OG 4.539580-11
~
-l
4 9 .483l-'D12
5 1.4aii40DB
1
2
3. 4874't7E-e5
1.~5Sl72E-Djj
1!1. o 0.1 J.042158Et00 ~.041mtOO 1. 706 779E +00 o.o
0.0 0.0 1. 109184[ +O '1 1. 109024(0 1 J.29163Ut00 0.0
3
~
7. 702li:U -QJ IUI 0.0 2.D~lOlEi11 1.8lt5004ED1 5.9922'13ECO o.o
'. l91391f.-IJZ 0.0 O.tl t1.99D49~00 8. 9:5857Jl DO 8.84!18370EOC O.D
5 1.510102Hl1 0.0 0.0 2. 15372.cE01 2. 14l6JU01 , 750105[01 D.D
1
2
5.6l6Z37E-04
3. 18:!6ll7E-13
0.1
0.1
5.9J97f1E+DI
6.ll4201Etl
5.t!l921fll l.:Ml795EOD 0.1
J 2.107867EDt 1.1 l!.l 6.46911)(+11
6.l39994EOI
4.273799Et1
4.856222[00
6.290112!01
D.l
"
5
3.41122!1!13
6.11Z501ED5
D.l
0.0
D.O
5.842155EIl
7 .]6]4Z2E +05
2.4l1511E03
1. 250896( 05
].469U~EtDS
1.116897~04
D.D
0.0
1
2
l
2. 228682(-G 1
1. 7842ft2E DD
1.lD42YlE02
0.1
o.o
0.1
ll.il
0.1
6. 71t4~5E lO
1.0ZCI 11HE;t
1.ft2~9!9ED2
6.521DIUIO
1.111575D5EOO
1.1972191:11
4.4!J0369hll
8.392955EOI
1.37172lf.IZ
li.D
0.1
0.1
4 ]. 1~6393E01 1.1 0.1
5 S.6ft603ftEOZ D.O 0.0
].1463931:111
5.6460ME02
D.O
t.764722f01
].!M2510E02
0.0
0.0
'5
!.Z49789E01
1. t 11111E03
:S.8169lfl+iH
6. BS8079E Ol
1. D966t5E OZ
1.'n0~5Etll3
6.2053E01
1. 118806E 03
9.55576aE06
7.68731DEOO
5.31M78E01
5.~3755(02
0.1
0.11
1
2
0.8
1.1 1.1
0.0
1.1 1.1 1.1
3
0.0
1.~5COOOE+iH
e.a O
I). 1.4500101+81
0.1
l.t
1.1
1.454011111
1.1
1.1
4 1.425000E+C1 11.8
~
1. 425800[. 01 1.1 1.~DIE+D1 t.l
!j G.D O.D cu 0.0 0.1
1.0
'
2.
]
B.G
11.1
D.D
D.l
D.l
8.1
C.ll
0.1
1.1
1.1
t.l
1.1
1.1
t.l
,,,I
l).t
't 0.11 t.l
0.1
1.1
o.o
1.11
5 5.oooaooEDt 0.0 0.1 5. DODDIHIE+et t.CI 5.0DOtcH+I1
D.O
Appeadh:F
Tabular Summ.ary ol Calculated Be!JUlJ
251
Table F.n.. Summary of calculated results (thick plate design).
LEU HEU
Core Size
Diameter (m) 0.81 0.88 0.65
Height (m) 0.98 1.08 0.79
Voll!llle (liters) 506.1 666.7 264.6
Buckling (cm-3) 3.4754xl0-3 2.8921xt03 5.3557x 1o-3
q"'~vg (kw/Jiter} 99 75 189
q"'max (kw/liter) 240 182 535
Bcmup(MWDm 28290 62120 548570
Burnup (at%) 3.0 6.6 57.9
252
Eud of Core Ufe (E,QQ
Final Fuel Enrichoxnt 4.3 13.9 68.1
U-235 number den:\ity (a/cm3) 8.9016x 102 2.093lx1021 1.4282xi()21
U-235 content (kg) 43.7 124.2 33.6
U-23ti numn.:z. <k.nsity (a!cm3)* l. 0482x 1()2 2.3891x1()20 5.9040xt02
U-236 content (kg) 3.1 14.2 14.0
U238 number density (aicm3~ l.7752xl()22 1.2SS4X i ()22 9.1914x10l9
U-238 content (kg) ~72 754 L75
Pu-239 number density (aJcm3)* 1.2042xl()20 1.4453xt()20 5.6331x1Q18
Pu-240 number density (afcm3)"' 2.4873x1019 2,5580xl019 1.5063x10 18
llu~241 number densiiy (afcm3) l.4070x1Ql~ l.7663xiQ19 2.6001x10 18
Pu-242 number density (afcm3) 1.6359xl018 1.7679x 10 18 9.9400x 10 17
Pu-239 contem (kg) 6.62 8.72 0.135
Pu-240 content (kg) 1.37 1.55 0.036
Pu-241 conten' (kg) 0.78 l.08 0.063
Pu-242 conteat (kg) 0.09 0.18 0.024
Puialll contem (kg) 8.86 11.45 0.262
&kfucl Lr:mp (Tfud 293K - 1000K) -0.026 -0.022 -0.007
Llkvoid (p(water) decrease 10%) -0.038 -0.028 -0.030
"' - The isotopic number densities lsred are for the fuel meat and are not averaged over lhe
core.
253
Table F.2. Sum.mary of calculated resulta (ATR type, thin plate design).
HEU HEU
(Regular Channel) (Thin Channel)
Core Sizst
Diameter (m) 0.74 0.70
Height (m) 0.90 0.86
Volume (liters) 384.6 333.3
Buckling (cm-3) 4.1732xiQ-3 4 .5909x 10-3
q"'avg (kw/liter) 131 150
q"'max (kw/liter) 368 425
Bwnup (MWDnJ 336160 382700
Bwnup (at%) 35.5 40.4
254
End of Core Lif~ CEQC
Final Fuel Enrichment 81.8
U-235 numbc:r density (a/cm3) 0 4.4455x 102 1 3.6650xJ()21
U-235 content (kg) 95.66 74.9
U-236 number density (a/cm1) 8.1154xi02
U-236 content (kg) 16.7
U-238 number density (a/cm3) 1.6026x 102
U-238 contem (kg) 3.3
Pu-239 number density (a/cm3) 1.5055x 10 19 1.4138xl019
Pu-240 number density (aJcm3) 2.7132x101R 2.6677x tQ18
Pu241 numberdensity (aJcm3) 3.8509x 101 7 4.3772xt018
Pu-242 number density (a/cm3) 5.4273x 1018 7.5292xt017
Pu-239 contem (kg) 0.330 0.294
Pu-240 content (kg) 0.012 0.056
Pu-241 content (k.g) 0.085 0.092
Pu-242 content (kg) 0.012 0.016
Putolal content (k.g) 0.437 0.457
Mc:ruc1 ternp (ffuel 293K- l()(X)K) -0.0043 -0.0051
Akvoid (p(water) decrease 10%) -0.025 -0.033
* - 'The isotopic number densities listed are for the fuel meat and are not averaged over lhe
core.
255
AppendixG
lmproved Reflector Savillp CaJculation l~thod
where
(G.2)
whe:te
256
For water, tis 27cm2. The thennal neutron diffusion areais defined as,
where
f = Thermal utilization
f= z
Z+l (G.4)
z = N.r2aF
NMO"aM (G.5)
where the subscripts F and M refers to the fuel and modera to r respectively.
As in earlier discussion, N and a refer to atom number density and
m.icroscopic neutron absorption cross-section respectively.
257