ML20097C651

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Univ. of Texas - Austin - Submittal of Neutronic and Thermal Hydraulic Analysis
ML20097C651
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Site: University of Texas at Austin
Issue date: 03/31/2020
From: Whaley P
University of Texas at Austin
To: Geoffrey Wertz
Document Control Desk, Office of Nuclear Reactor Regulation
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Download: ML20097C651 (27)


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WALKER DEPARTMENT OF MECHANICAL ENGINEERING Nuclear Engineering Teaching Laboratory Pickle Research Campus R-9000

  • 512-232-5380
  • FAX 512-471-4589 nuclear. engr. utexas. edu
  • wcharlton@austin. utexas. edu March 31, 2020 ATTN: Document Control Desk U.S. Nuclear Regulatory Commission Washington, D.C. 20555-0001 Geoffrey Wertz, P.E.

Non-Power Production and Utilization Facility Licensing Branch Division of Advance Reactors and Non-Power Utilization Nuclear Reactor Regulation

SUBJECT:

Docket No. 50-602, Facility Operating License R-129 - Submission of Neutronic and Thermal Hydraulic Analysis for the University of Texas at Austin Research Reactor

REFERENCE:

October 18, 2018 letter: University- of Texas at Austin - Summary of Site Visit and Request for Schedule for Completion of the Reactor Analyses RE: Renewal of Facility Operating License No.

R-129 for The University ofTexas at Austin Research Reactor (EPID NO. L-2017-RNW -0032)

Sir:

We respectfully submit neutronics and thermal-hydraulic analysis, attached. If you have any questions, please contact me at 512-232-5373 or whaley@mail.utexas.edu.

P. M. Whaley I declare under penalty of perjury that the foregoing is true and correct.

W. S. Charlton ATT:

(1) Analysis of the Neutronic Behavior of the Nuclear Engineering Teaching Laboratory at the University of Texas (2) Thermal Hydraulic Analysis of the University of Texas (UT) TRI GA Reactor

THERMAL HYDRAULIC ANALYSIS OF THE UNIVERSITY OF TEXAS (UT) TRIGA REACTOR Paul (Michael) Whaley and William S. Charlton Nuclear Engineering Teaching Laboratory University of Texas at Austin Austin, TX 78758 March 31. 2020 1

1.0 INTRODUCTION

This report documents analysis of the thermal hydraulic characteristics of the UT TRIGA nuclear research reactor in support of renewal of the U.S. Nuclear Regulatory Commission facility operating license. NRC guidance 1 specifies definition of a limiting core configuration (LCC) as the core that would yield the highest power density using the fuel specified for the reactor, with all other core configurations encompassed by

  • safety analysis for the LCC. Coupled analyses for neutronic and thermal hydraulic behavior are used to characterize thermal hydraulic performance of the LCC. This report describes the thermal hydraulic analysis, .

the neutronic analysis is a separate report 2

  • Heat generated by fission in operation of the UT TRIGA reactor is transferred by conduction from the fuel to the cladding. The fuel cladding is the principal safety feature of the TRIGA reactor, preventing radioactive fission products from release that could result in possible hazardous exposure to radiation for facility personnel and the general public. The integrity of the fuel cladding is assured if the fuel temperature remains below specific values (830°C during pulsing3, 950°C if the cladding temperature is less than S00°C, and 1150°C if the cladding temperature is above S00°C4 ).

Heat is transferred to water [or air in the case of a loss of coolant accident (LOCA)] surrounding the fuel element cladding. The cooling medium temperature increase develops buoyancy forces that drive convection flow. Cooling flow is impeded by momentum changes and friction (across the grid plates, fuel element end fittings, and fuel element cladding surfaces). Above a "critical" heat flux (CHF), cooling flow may not* be adequate to prevent exceeding the temperature limits, and 'burnout' will occur. The NRC guidance limits the ratio of heat flux to critical heat flux (CHFR) to a value greater than 2.0. A correlation for CHFR applicable to TRIGA reactors has been developed by Bernath 5 and is used in this analysis.

The fuel element in the LCC that operates closest to the limits is the element generating the most power,

'hot channel. Analysis of the hot channel demonstrates that operation at.the maximum licensed power level and within licensed reactivity limits maintains the reactor fuel below the temperature limits, and heat transfer to the surrounding cooling media remains above the CHFR limit.

TRACE (TRAC/RELAP Advanced Computational Engine) is the NRC's flagship thermal-hydraulics analysis tool consolidating and extending the capabilities of NRC's three legacy safety codes: TRAC-P, TRAC-B and RELAP. These codes are designed to perform best-estimate analyses of operational transients and accident scenarios by modeling physical geometry and thermodynamic conditions. TRACE and RELAP were developed for commercial nuclear reactors applications, and RELAP has also been widely used in characterizing non-power/research reactor thermal hydraulic performance.

Thermal hydraulic modeling of the hot channel in the UT TRIGA reactor was performed using TRACE. The model was developed using standard, classical methods applied to the fuel element geometry and fuel element pitch. However, fuel element construction includes complex end fittings not well represented in modeling flow resistance classically, and coefficients characterizing the resistance to cooling flow for the UT 1

NURGE 1537, Guidelines for Preparing and Reviewing Applications for the Licensing of Non-Power Reactors, Format and Content 2

Analysis of the Neutronic Behavior of the Nuclear Engineering Teaching Laboratory at The University of Texas, Radiation Center - Oregon State University 3

TRD-070-0.1006.05 Rev A, Pulsing Temperature Limit for TR/GA Fuel (TRIGA Reactors Division of General Atomics-ESI, 2008) 4 NUREG/CR-2387 Credible Accident Analyses for TR/GA and TR/GA-Fueled Reactors (PNL-4028, April 1962) 5 ANL RETR TM 07 01, Fundamental Approach to TRIA Steady-State Thermal-Hydraulic CHF Analysis, E. E. Feldman (2007) 2

TRIGA were therefore developed in the computational fluid dynamics code FLUENT. 6 Data in TRACE output files were parsed to identify maximum fuel temperature and variables used in the Bernath correlation.

TRACE has an internal library of standard material properties relevant to power reactors. The library does not include properties for zirconium and TRIGA fuel; these material characteristics are supplied as manual input. The ratio of the maximum power in the hot channel to average core-wide element power (peaking factor, developed from the neutronics analysis} is used to extend transient calculations from elements generating core average power to calculations for the element generating the maximum power in the core.

An estimate of the prompt neutron lifetime was generated in an MCNP adjoint calculation to support reactivity calculations in TRACE.

An auxiliary program distributed with MCNP (MAKXS} was used to generate neutron interaction cross sections at specific fuel and water temperatures. These cross sections were used in MCNP criticality calculations to develop reactivity temperature-coefficients for TRACE reactivity calculations. The MCNP model developed in the neutronics analysis was used to generate delayed neutron precursor constants. The constants were used to develop time-dependent heat generation from fission following shutdown for LOCA analysis. The heat generation from fission product decay for LOCA analysis was developed from the method described in ANSI/ANS~5.1-2014, Decay Heat Power in Light Water Reactors. Heat generated from neutron interaction with fission products was neglected.

Analyses were developed to characterize performance associated with steady-state operation, reactor pulsing, continuous control rod withdrawal transients, and a LOCA. Validation of the modeling was performed by comparing analytic results to peak temperatures during steady state operations, and power levels and temperatures that occurred during pulsing operation. The model was validated and then used to develop the LCC.

2.0 TRACE MODEL The TRACE model uses 'break' elements that establish pressure and temperature fluid boundary conditions.

Pool water is delivered from break through a 'downcomer' with a horizontal structure connecting the downcomer to the inlet of the fuel element flow channel. The fuel element flow channel discharges to another break. A conceptual diagram of the model is provided in Fig. 1.

2.1 Flow Channel Geometry The cooling flow channel is modeled as a heated pipe with thermodynamic characteristics based on physical dimensions and properties of the coolant surrounding the fuel elements .. The outer diameter of a fuel element (DF} is 1.475 in. The outer diameter of the fuel is 1.435 in. with an inner diameter of 0.25 in. filled with a 0.225 in. diameter zirconium rod. The cladding is 0.020 in. thick, with a small gap between the inner cladding diameter and the fuel outer diameter. The center-to-center distance to adjacent elements (pitch, Pe} is 1.714 in.

6 (Doctoral Dissertation) Development of thermal Hydraulic Correlations for the University of Texas at Austin TRIGA Reactor Using Computational Fluid Dynamics and In-Core measurements, A. D. Brand (2013),

https://repositories.lib.utexas.edu/handle/2152/23039 3

Inlet Outlet Break Break Figure 1: UT TRACE Model The geometry of the fuel element and surrounding flow area (Figs. 2 and 3) is modeled as a hexagon with an inner radius (i.e., the largest circle centered in and bounded by the hexagon) of Yi of the pitch. A la rge fraction of the model is occupied by the fuel element, leaving a relatively small flow area. End fittings have more complex geometry and are approximated using hydrodynamic characteristics.

COOLIN G WATER CLADDING Zr FILL ROD Figure 2: Flow Channel for UT TRIGA The area of the flow channel (A) is the area of the hexagon less the area of a fuel element. Using Pe as pitch and OF as the diameter of the fuel element, the area of the flow channel is given by:

A=";. p; - rr. (D;) 2 Eqn 1 The wetted perimeter (Pw) is the perimeter of the fuel element:

Eqn 2 4

Flow Adjacent Channel Fuel with Element Area A Figure 3: Pitch and Fuel Element Diameter An d Relation to Flow Channel Non-circular pipes are approximated from the flow area and the wetted perimeter (Pw) with an equivalent hydraulic diameter (Dh) calculated using:

4 *A Dh = - - Eqn 3 Pw Substituting equations 1 and 2 into equation 3 yields the following for the hydraulic diameter:

D= 4 h 1[

  • DF*[.J3 2*p2 -1l *(DF2)2]= 2*.J3. DFp; -DF=DF*[.J32.Dip; -1]

e 1[

Eqn 4 Equations 1-4 are used the TRACE modeling.

2.2 Thermal Hydraulic Loss Factors Pressure drops (head loss) across hydraulic components are the product of the fluid flow and factors such as the coefficient of friction between the fluid and the pipe wall, changes in flow area and diameter, flow channel surface roughness, and/or flow channel length. Standard practice defines the characteristics that determine head loss as coefficients, or K factors based on experimentally derived correlations to support conservation of energy and momentum calculatio ns for fluid flow . The surface roughness for TRIGA fuel elements is 6.998E-6 ft. 7 Correlation of K factors with geometry and flow are based on historical, experimental measurements with cylindrical pipes. Additional work extended this to rectangular ducts; non-circular cross sections are reduced to a flow area and hydraulic diameter developed as circular geometry.

These correlations apply after flow is fully developed following geometry perturbations that create turbulence. The geometry inherent in TRIGA fuel challenges appli cation of standard formula to calculate the Kfactors:

  • The actual entrance and exit to the flow channel between the grid plates is directed by fins, a center pin, and a conical shape with part of the structure extending into the volume bounded by grid plate penetrations; the wetted perimeters vary continuously from entrance to exit for each end fitting.
  • The fuel element end fittings are partially inserted in grid plate penetrations that fix the position of 7

Oregon State University, Model Editor File for the OSTR thermal hydraulic Model (private communication) 5

the fuel elements in the core, causing area expa nsion and contraction over parts of the end fittings at the entrance and exit of the upper an d lower grid plates.

  • The interface between adjacent fuel channels is not separated by a physical boundary, and differential pressure between adjacent flow cha nnels can support cross-channel flow, although analysis has shown that any cross-flow is small and has "no effect on fuel temperature" with a slight increase in critical heat flux ratio 8; cross flow is neglected in this analysis.

Therefore, thermal hydraulic analysis to support relicensin g was developed to independently model thermal hydraulic performance at the end fittings from (1) first principles, (2) the TRACE therm al hydraulics code, and (3) the FLUENT computational fluid dynamics code. The results of experiments in the TRIGA core were used to evaluate UT TRIGA-specific K factors based on actual fuel element geometry. The values determined from the UT research program (Table 1) were used in modeling for TRACE calculations.

Table 1: UT TRIGA Specific K Factors APPLICATION K Factor TRIGA Lower Ch annel 1.63 TRIGA Upper Channel 1.12 2.3 Hydrostatic Pressure The cooling pressure and temperature specifications in the break components are based on local environmental conditions (barometric pressure, confinement pressure regulation) and the pool {level and water temperature). The NETL building is approxim ately 240 m above sea level, and the reactor bay confinement system is designed to control differential pressure to 0.06 in. below atmospheric pressure (minimal compared to atmospheric pressure). Total pressure at the top of the core is:

Eqn 5 Pool water is nominally 7.25 m, with a minimum of 5.25 m above the core. Pool water temperature is nominally 25-27 °C, and limited to less than 49 °C. W here g denotes the gravitational constant {9.8 m*s*2 ),

the pressure (pH20) exerted by a column of water (at density p in kg*m* 2and height h in m) is given by:

Eqn 6 A break is also connected to the exit of the core, representing exit from the flow channel to the same parameters as the entrance. Pressure boundary conditio ns for the limiting cases are provided in Table 2, converted to British units for TRACE input.

Table 2: LCC Temperature & Pressure Temp Pressure Condition

(°F) (Psia)

Limiting 120.2 21.3 Nominal 77 24.2 8

Armed Forces Radiobiology Research Institute (AFRRI) submittal of Safety Analysis Chapters 4 and 13 to the USN RC (ML101650422, submitted on March 4, 2010) 6

2.4 Heat Structure Modeling The heated length of the fuel element is modeled as a TRACE heat structure. Heat structure cells simulate the zirconium fill rod at the center of the fuel element, the fuel matrix, the gap between the fuel and cladding, and the cladding. The UT TRIGA heat structure consists of 15 axial cells that transmit heat from the fuel element to the cooling channel. The UT TRIGA model uses a gas gap heat transfer coefficient9 of 500 Btu h-1 tt-- 2 T1, (2840 W m-2 K-1 ). The flow channel includes non-heated lengths that are not part ofthe heat structure above and below the heated length representing integral graphite reflector and end fittings (with a space in the upper end fitting for fission gas collection incorporated above the upper graphite reflector).

2.5 Power/Reactivity Application Fuel element power is used as an input for steady-state and LOCA analysis, and it supports cases with time-dependent reactivity variation. Reactivity is used as an input for transient analysis (pulsing and control rod withdrawal transient analyses). Reactivity transients are used to generate power levels at times for a fuel element representing the core average in* pulsing and control rod withdrawal analysis; then the time dependent average element power level is scaled by the core peaking factor to represent the hot channel in a time dependent power calculation. For LOCA analysis, the time dependent behavior of power following shutdown was evaluated and developed using reactor kinetics for fission power and for decay heat from fission product using the method of ANSI/ANS-5.1-2014 (equation 7 and 8). For an irradiation interval of time T, a decay time oft, and irradiation intervals i and a constant fission rate of unity, decay heat power (F, units of MeV/fission) can be represented analytically as a function using analytic fit constants a and /3 (the fit constants are provided for all 23 components in the standard):

23 Fi(t, Ta)= L:~*~

  • j=l l,]

exp(-ili,j

  • t) * [1- exp (-ili,j
  • T)] Eqn 7 Assuming a single power generation interval and a long operating time, this reduces to:

23 a*

F(t) = L _}_

il-j=l J

  • exp(-ili
  • t) Eqn 8 The ratio of decay heat power to initial reactor power depends on a reactor specific energy generation per fission (MeV/fission) that is also used in TRACE transient calculations. The MCNP burnup analysis output tabulates fission energy yield data (Q value, Table 3) as given in Table 3.

Table 3: Fission Energy Yield from MCNP Analysis Nuclide Q-Value (MeV) 92235 180.88 92238 181.31 94239 189.44 94241 188.99 9

The University of Texas Safety Analysis Report, Revision 1.01 (5/91) 7

--- -~----

l 1

The fraction of energy produced by each fissionable material (Table 4) is taken from an MCNP burnup calculation supporting the neutronics report for use in TRACE analysis. Estimates of the fraction of isotope 92235 fissions at greater than thermal energy are assumed to have Q values consistent with isotope 92238.

Table 4: Fission Isotope Nuclear Characteristics 10 Fission Fissions at Nuclide Fraction Cross-section Energy Range Energy (b) 585.1 <0.625 eV 94.28%

92235 19.8%

274.4 0.625 ev - 100 kev 4.99%

1.241 92238 80.2%

0.03064 >100 kev 0.72%

The kinetics treatment used fission product nuclear characteristics (precursor fractions, decay constants, and the generation time) from MCNP adjoint calculations given in Table 5. Thermal/non-thermal fission fractions are taken from the MCNP burn up calculations.

Table 5: Delayed Neutron Precursor Group Characteristics p; Standard Energy Standard A; Standard T112 Standard Deviation (MeV) Deviation (s-1) Deviation (s) Deviation 1 0.00022 0.00005 0.40605 , 0.00460 0.01334 0.00000 51.960 0.004 2 0.00138 0.00013 0.47218 0.00202 0.03273 0.00000 21.178 0.001 3 0.00138* 0.00012 0.44217 0.00202 0.12080 0.00000 5.73797 0.00005 4 0.00296 0.00019 0.55867 0.00181 0.30295 0.00001 2.28799 0.00008 5 0.00113 0.00011 0.51895 0.00294 0.85032 0.00004 0.81516 0.00004 6 0.00059 0.00009 0.53926 0.00495 2.85537 0.00021 0.24227 0.00002 Heat generation distribution in the heat structure is based on mesh tally calculations from MCNP modeling described in the neutronics report. The mesh tally provides average fission density at 225 locations throughout the fuel rod. These 225 locations consist of equal volume segments of the fuel with 15 radial segments and 15 axial segments. The normalized mesh values were applied to locations in TRACE. Equal volume segments were allow direct averaging of temperatures in the fuel. This 15x15 matrix was used as a power distribution profile in TRACE.

MCNP calculations were used to acquire estimates of the prompt neutron generation time and effective delayed neutron fractions. The MCNP calculations produced an estimated prompt-neutron generation time of 43.81+/-0.53 µs (Table 6). The 1992 Safety Analysis Report for the UT TRIGA cited a prompt generation time of 41 µs, which is consistent with that calculated by MCNP. For the purposes of this report the MCNP calculated value was considered to be more applicable since it utilized current parameters.

The effective delayed neutron fraction has historically been used as 0.007 for the UT TRIGA. The MCNP calculated value for Pett was 0.00737+/-0.00006 (Table 6). Calculating pulsing reactivity in units of$ based on Pett of 0.007, and therefore represents 91% of the nominal pulsed reactivity. Data from two series of reactor pulses with varying reactivities were analyzed using the Fuchs-Hansen pulse model modified to evaluate Pett 10 https://wwwndc.jaea.go.jp, Fission at Energy from MCNP burn up calculation 8

J

from the convergence of itera~ive calculations. Pulses from November 2018 were found to have a ~eff of 0.007306, and from March 2020 to have a ~eff of 0.007382. Therefore, a correction is necessary in model validation against historical data.

Table 6: MCNP Calculated Reactivity Parameters Standard Parameter Estimate Deviation Generation Time 43.81 µs 0.53 µs

~eff 0.00737 0.00006 2.6 User Defined Materials Zirconium properties are provided in Table 7. The zirconium fill rod is slightly smaller than the center hole of the fuel element. Therefore, the standard zirconium density was reduced by the ratio of the zirconium rod volume to the whole volume.

Table 7: Zirconium Properties Temperature Density Heat Capacity (Cp) Thermal Conductivity Emissivity OF lbm/ft3 Btu/lbm-°F Btu/h-ft-°F

-99.4 328.18 0.082284 14.562 0.8 260.6 328.18 0.102199 12.4812 0.8 620.6 328.18 0.122114 11.9592 0.8 980.6 328.18 0.142029 12.4812 0.8 1340.6 328.18 0.161943 13.6944 0.8 1700.6 328.18 0.181858 15.0228 0.8 2240.6 328.18 0.211731 16.6392 0.8 4481.2 328.18 0.335679 21.6392 0.8 Reference values 11 for specific heat capacity (Cp) and thermal conductivity (kc)of TRIGA fuel are:

  • Cp = 0.018 +/- 0.009 watts [cm-10 C-1]
  • kc= 2.04 + 0.00417 x T [W s-1 cm-3 C- 1] (note that this is given as a function of material 0

temperature T)

These formulae were converted to British units and used to generate tabular values (Table 8} for TRACE.

11 E-117-833, The U-Zrx Alloy: Its Properties and Use in TRIGA Fuel (Simnad, General Atomics Project No. 4314) 9

Table 8: Uranium-Zirconium Hydride (Fuel)

Temperature Density Heat Capacity (Cp) Thermal Conductivity Emissivity OF lbm/ft3 Btu/lbm-°F Btu/h-ft-°F

-65.6 374.5 0.029754 10.16021 0.8 294.4 374.5 0.091403 10.16021 0.8 654.4 374.5 0.153051 10.16021 0.8 1014.4 374.5 0.2147 10.16021 0.8 1374.4 374.5 0.276349 10.16021 0.8 1734.4 374.5 0.337997 10.16021 0.8 2274.4 374.5 0.43047 10.16021 0.8 4548.8 374.5 ' 0.814165 10.16021 0.8 2.7 Temperature Feedback Temperature feedback is incorporated in the transient analysis for pulsing and control rod withdrawal events. General Atomics 12 indicates that the fuel temperature coefficient (water reflected) is convex, with a minimum occurring about 300°C. An analysis at AFRRl 13 based on DIF3D (Argonne National Laboratory, diffusion and transport theory code) calculations show convex structure from 10-1000°C for TRIGA fuel.

Standard MCNP cross sections are available in intervals of about 300°C; it is not possible to get data from calculations where cross-sections are separated by 300°C that would provide accurate data for derivation of cross sections. Therefore, an auxiliary code distributed with MCNP (MAKXSF) was used to generate data over the range for operations of interest. Although fuel temperature and water temperature coefficients are generally considered independently, they are coupled. The temperatures used for generating these cross sections are shown in Table 9.

Table 9: Cross Section Temperatures (°F)

Fuel 98.33 118.13 344.93 458.33 571.73 841.73 1111.73 1291.73 1471.73 1651.73 Water 76.73 76.73 80.33 107.33 134.33 168.53 188.33 215.33 Criticality calculations with the MCNP model developed in the neutronics analysis were performed using all permutations of temperatures indicated. Fuel temperature, water temperature, and the associated excess reactivity for each calculation was used to generate a function of the two temperatures. The function was

-used to evaluate values Yi degree above and Yi degree below specific fuel temperatures with water temperature held constant, and then varying water temperature with constant fuel temperatures. The results are provided graphically at selected fuel temperatures, fuel temperature reactivity coefficients for a series of constant moderator temperatures (Fig. 4) and moderator temperature coefficients for a series of constant fuel temperatures (Fig. 5).

12 Simnad op. cit.

13 AFRRI op. cit.

10

-6.0E-05

~ -7.0E-05 L.

Q)

C.

~

~ -8 .OE-05 I,()

j::' -9.0E-05 z

UJ u

LL

-l.OE-04 LL UJ 8 -1.lE-04

~

j:::

-l.2E-04 u

~ -1.3E-04 0:::

-l.4E-04 0 200 400 600 800 1000 FUEL TEMPERATURE (0 C)

--24.85 --26.85 --41.85 --56.85 --75.85 --86.85 -- 101.85 --116.85 Figure 4: Temperature Coefficient of Reactivity for the Fuel Versus Fuel Temperature (shown at a variety of fixed coolant temperatures) l.OE-05 u O.OE+OO 0

CII c.. -l.OE-05

.ll::

~ -2.0E-05 IO zw -3.0E-05 0

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LI.

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0 u -5.0E-05

~ -6.0E-05 6 -7.0E-05

~

a:

-8.0E-05 20 40 60 80 100 120 WATER MODERATOR TEMPERATURE(°C)

+ FT,25C ~ FT,48C ... FT,800C +- FT,900C Figure 5: Water Temperature Coefficient of Reactivity Versus Water Moderator Temperature (shown at a variety of fixed fuel temperatures) 11

The maximum variation in the fuel temperature reactivity coefficient at low temperature (with respect to water temperature) is on the order of 10% from nominal water temperature to temperatures near boiling in the core. The water temperature change is dominated by the decrease in water density as temperature increases; lower water density increases scattering length and reduces moderation in the cooling channels.

As fuel temperature increases there is less absorption in the fuel matrix and consequently more neutron scattering out of the fuel matrix into the water. These competing effects cause the difference with respect to water temperature to converge and then reverse the difference at higher fuel temperatures where the neutron spectrum is hardened in the fuel to shift moderation to the water region. With a constant fuel temperature, the moderator temperature coefficient change is almost linear with respect to moderator temperature change from am bient temperature values to near boiling for hydrostatic pressure in the core.

The calculations based on DIF3D 14 suggest fuel coefficient reactivity ranges from -8x10-5 to -1.2x10-4 6k/k °C 1

for a TRIGA core with a circular grid plate (the UT TRIGA has hexagonal pitch), or -4.5x10-5 and -6.8x10-5 6k/k °F-1 . This is in reasonable agreemen t with this analysis. The temperature coefficient data is used in TRACE to determine feedback for transient analysis.

3.0 VALIDATION The neutronics report identifies instrumented elements in core positions B03 and BOG as generating 15.82 kW and 15.39 kW respectively in a 1.1 MW core of 113 elements (based on the MCNP calculations). The UT TRIGA administratively limits power operation to 950 kW, 86.4% of the licensed power level; therefore, the power levels generated in the thermocouple elements at nominal full power operations are 13.66 kW and 13.29 kW. Normal operations occur with a pool (cooling water) temperature of 25°C (77°F) where the limiting core condition assumes 49°C (120°F). Pool level during normal operations is 5.25 m (23.8 ft) above the core while the limiting core condition is 5.25 m (17.2 ft) above the core; hydrostatic pressure is 24.2 psia for normal operations, 21.3 psia for limiting core conditions. A series of calculations using nominal conditions was performed to allow comparison of observed power levels and temperatures to those generated by the TRACE model.

3.1 Steady State The temperature of the location for each of the three thermocouples in the instrumented fuel elements were calculated using the TRACE model, with the thermocouples in each instrumented fuel element deviating by about 13°C (Table 10). Fuel temperature channel readings were taken from records of operation in December 2018 at 950 kW and compared to TRACE calculations (Table 10). Fuel temperature channel indications were 420°C (FTl) and 334°C (FT2). The highest fuel measuring channel indicated 7.3% above the maximum temperature calculated with MCNP/TRACE data, the lowest IFE channel indicated 10% higher th an the lowest indication on the fuel temperature measuring channels. The highest temperature calculated with the TRACE model is about 7% lower than the fuel tem pe rature measuring channel indication, and lowest temperature is about 10% higher.

The difference between the TRACE data from the thermocouples in each IFE is attributed to the axial position of the thermocouples (separated by 1 in. above and below the center thermocouple). There are no records correlating individual thermocouples with specific axial position (although lead wire labeling suggests the center thermocouple may be identifiable). Data calcu lated at each thermocouple position are therefore included in Table 10.

14 AFRRI op cit.

12

Table 10: Comparison of MCNP/TRACE Calculations and Fuel Temperature Measuring Channel Indications Element MCNP/TRACE Fuel Temp Deviation Power (kW) TC Temps Channels 389.03°C -7.37%

13.66 387.00°C 420°C -7.86%

376.03°C -10.47%

380.41°C 13.89%

13.29 378.41 °C 334°c 13.30%

367.70°C 10.09%

Comparison of the TRACE calculation and observed data shows reasonably close agreement, with differences that may be partially attributed to IFE fabrication and coupling with the MCNP model. The channels in the fuel meat accommodating the thermocouples reduce the mass of the fuel in the elements slightly, which was not modeled in MCNP. One ofthe fuel elements was installed in 2018, with the fresh fuel and the gap between fuel and cladding expected to cause elevated temperatures until the fuel has achieved significant burn up. The calculated temperatures are in reasonable agreement with measured data.

3.2 Pulsing Operations The TRACE calculations were compared to historical data to validate the accuracy of the method used.

Historical pulse data (reactivity addition, peak pulse power, and maximum temperature from the fuel temperature measuring channels) was compiled, with incomplete data purged. There is significant scatter in power level (Fig. 6) and temperature (Fig. 7) data with some outliers but the results overall provide a good validation. Pulse records do not include factors with potential to affect pulse characteristics such as initial fuel temperature, pool temperature, or recent operating history that might explain some of the scatter in the data. The TRACE calculations are for individual elements, so peak power level during pulses was distributed across the core for comparison to historical data. Although there is significant scatter and outliers in historical pulse power level data, it is clear that qualitatively the TRACE data agrees well with historical data.

A comparison of peak temperature to historical pulsing data required adjusting the average pulse power to the power generated in the IFE by the ratio of the power in the instrumented fuel elements (identified in the neutronics report) to the average element power. The fuel matrix in IFEs is fabricated with milled channels to accommodate thermocouple leads, and the thermocouples are installed in fuel penetrations extending form the outer surface to near the inner surface of the fuel. Consequently, the volume of the fuel in the IFE is a few percent lower than a standard fuel element. All fuel material specifications in the MCNP model used to calculate power generated in the IFE assumed the same density as standard fuel elements, likely resulting in a higher power generation. It is therefore expected that the peak pulse fuel temperature in the IFEs calculated from MCNP and TRACE (Fig. 7) is slightly higher than historical values. Even with the complications created by MCNP modeling, data scatter, and outliers the TRACE calculations agree well with observed data.

13

2.SOE+07 2.00E+07 D D

I 1.SOE+07 i.

t E D GI uj l.OOE+07

~

l'G 5.00E+06 O.OOE+OO D = ~

$1.00 $1.50 $2.00 $2 .50 $3 .00 Pulsed Reactivity Addition ($)

a Historical Observed Data o TRACE Figure 6: Peak Element Power Level Versus Pulse Reactivity Addition from UT TRACE Calculation Compared to Observed Historical Data 450 400 i;g D qi D

D 350 g D

t300 Q)

'ii) 250 QI a.

E 200

~

.:,,(.

CL i 150 100 D so 0

$1.00 $1.50 $2.00 $2.50 $3 .00 Pulse Reactivity Addition($)

o Historical Observed Data O TRACE Figure 7: Peak Fuel Temperature Versus Pulse Reactivity Addition from UT TRACE Calculation Compared to Historical Data 14

3.3 Conclusion Fuel temperatures indicated by the fuel temperature measuring channels, and power and temperature from historical records of pulsing, were compared to data generated with TRACE calculations. The comparison demonstrates that the TRACE model is capable of predicting thermal hydraulic performance of the UT TRIGA reactor with reasonable accuracy.

4.0 LIMITING CORE CONFIGURATION 4.1 Steady-State Power Level The neutronic analysis indicates that for a licensed power of 1.1 MW, the maximum power in any element is 22.14 kW with 84 elements. With a maximum potential instrument error of 10%, the maximum power in the hot channel could be as high as 24.34 kW. UT TRIGA hot channel power level in this report is well within TRIGA operating experience, less than reported values for the AFFRI TRIGA reactor (35.3 kW) and the TRIGA conversion reactor at the University of Wisconsin (26.04 kW) 15, and less than the 30 kW value cited in ANL RERTR TM 07 01 (which references the MNCR reactor at 33.2 kW).

To evaluate steady-state performance of the LCC, a series of TRACE calculations were performed for the UT TRIGA for fuel element power levels between 5 kW and 60 kW under limiting core conditions. Temperature dependence of the fuel versus power is shown in Fig. 8 for the hot channel, while the radial and axial distribution across the hot channel are shown in Figs. 9 and 10. Fuel element power at 44.9 kW is found to result in a maximum fuel temperature during steady state operations of 1149.9°C, essentially the maximum safety limit if cladding temperate is less than S00°C. Fuel element power at 36.6 kW results in 948.1 °C, approaching the 950°C safety limit if cladding te mperature is greater than S00°C.

1200 1100 1000 u 900 0

Q) 800 700

~ 600 Q)

a. 500 E 400

~

300 200 100 0

0 5 10 15 20 25 30 35 40 45 50 55 Fuel Element Power Level (kW}

- o- IFE - TCl **-.t:1** IFE - TC2 __. MAX FT Figure 8: LCC Steady-State Fuel Temperature Versus Fuel Element Power at Each Thermocouple and at the Maxim um Fuel Temperature Location 15 University of Wisconsin LEU Conversion Report (Request for Amendment No. 17 to Faci lity License No. R-17, 08/25/2008) 15

800 700 0-------- Clad 600 Zirc

+-- Fill -

~ 500 Rod GJ to

.... 400 GJ 0.

E

~ 300 Fuel 200 100 0

0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 Distance from Rod Center (in.)

Figure 9: LCC Hot Channel Radial Fuel Temperature Profile at Hottest Axia l Position 800 700 600 u

0

~ 500

~

GJ 400 0.

E GJ

!::GJ 300 LL.

200 100 0

0.0 2.0 4.0 6.0 8.0 10.0 12.0 14.0 16.0 Elevation from Bottom of the Element (in.)

o Hottest Channel

  • Average Channel Figure 10: LCC Hot Channel Axial Radial Fuel Temperature Profile 16

The critical heat flux that leads to burnout is calculated by the Bernath correlation {with variables defined in Table 11):

Table 11: Bernath Correlation Variables De Hydraulic diameter ft Previous formula D; Heater surface diameter ft Fuel element diameter V Pressure Psia Calculated by TRACE p Velocity ft*s* 1 Calculated by TRACE Ts Coolant Temperature oc Calculated by TRACE A series of calculations were performed using the Bernath correlation to determine the relationship between element power and the minimum CHFR along a rod in limiting core conditions (Fig. 11). The limiting value of 2.0 for CHFR occurs at 56 kW generated in the hot channel, in agreement with analysis cited in ANL RERTR TM 07 01. With the UT TRIGA hot channel operating at 24.35, the critical heat flux ratio is 4.69.

25 23 21 19 17 0

ro a:: 15 X

13 U:::

ro QJ 11

z::

ro 9 u

  • 7 ***o.

u ***o ~

5 *00¢ ..

3 ~..... () .......

" ¢ ............ ~ ........... ~ ............¢ 1

0 5 10 15 20 25 30 35 40 45 so 55 60 65 Element Power Level {kW)

Figure 11: CHFR (Bernath Correlation) Versus Fuel Element Power The critical heat flux ratio varies along th e length of the hot channel fuel element at full power as indicated in Fig 12. The minimum CHFR is slightly above the center of the section of the fuel element that contains fuel.

17

10.0 o.

9.0 0

.:; 8.0 ro er:

X

?

.
o.

ro 7.0 (1/

c:

iii u

.:; o. .
  • .: 6.0 u

.. ~

Q /

                    • o ..9...

5.0 **.. .....**

.o-**

              • O..........O*********o**********o*********

4.0 0.0 2.0 4.0 6.0 8.0 10.0 12.0 14.0 16.0 Elevation Along Heated Length (in.)

Figure 12: CHFR Hot Channel Axial Values from the Bernath Correlation for UT TRIGA Fuel Element Operating at 24.34 kW With the hot channel operating at 24.34 kW, the maximum temperature in the core is calculated to be 650°C, approximately 300°C below the 950°C safety lim it (68% of the limit). The hot channel element CHFR with power level of 24.34 kW is 4.69 which is significantly above the CHFR limit of 2.0. The power level that would result in a CH FR of 2.0 is at 55 kW which gives significant factor of safety.

4.2 Pulsing Operations Pulsing reactivity calculations were performed in TRACE for $3, $4, $5, $6, and $7 insertions with initial conditions approximating shutdown power levels. The calculations were performed in two steps: (1) using reactivity to calculate time-dependent core power level and (2) using the time/power profile for the second step (with the power of the second step scaled by the hot channel peaking factor). The peak power as a function of pulsed reactivity is shown in Fig. 13, and th e time-development of the power pulse for the reactivity insertions in Fig. 14. Note that the $7 insertion were high enough compared to the other insertions that it was not included so that the remai ning data can be shown on a reasonable scale.

18

l.6E+08 I I I

1.4E+08 v, l.2E+08 ,,

i:: , ,,

ro

~... l.OE+08 ,,

Cl/

3 ,,

0 a.

Cl/

8.0E+07 VI

a. 6.0E+07 ,,

E E 4.0E+07

  • x ro

~

2.0E+07 O.OE+OO

$2.50 $3.00 $3.50 $4.00 $4.50 $5.00 $5.50 $6.00 $6.50 Pulse Reactivity Insertion Figure 13: Hot Channel LCC Peak Power Level Versus Reactivity Insertion l.60E+08 l.40E+08 1.20E+08 f ro 1.00E+08

~ ... 8.00E+07 ,' \

Cl/ I \

3 I \

g_ 6.00E+07 I \

I I

I I I I I

4.00E+07 I I I ,

I I \ _,.

2.00E+07 I I

V

\

I I

I \

O.OOE+OO 1.02 1.04 1.06 1.08 Time {s)


$3.00 - *- $4.00 --- $5.00 -$6.00 Figure 14: LCC Pulse Power Versus Time for Varying Reactivity Insertions A $3 insertion resulted in a peak temperature of 378°C. As shown in Fig. 15, the temperature limit was not exceeded for any reactivity insertions below $6 {with a 130°C or 16% margin at $6). The temperature safety limit was not exceeded at a $7. Time dependent behavior is shown in Fig. 16.

19

750 700 650 E6oo

~

I

..... 550

~

Q) a.

E 500

~

a:i

I 450 LI..

400 350 300

$2.50 $3.00 $3.50 $4.00 $4.50 $5.00 $5.50 $6.00 $6.50 Pulse Reactivity Figure 15: LCC Hot Channel Peak Fuel Temperature Versus Pulse Reactivity Addition 825 725 625

.u 525

~

C1I

'/.*,**. - .-*-*-*-*-*- -*- - - *- -*-*-*-*-*-*-*-*-*-*-*-*-*-*-*- -

  • t'. 425 n,  : *'

..,./!'. ,' , , ,,---------------------------------------------

~

C1I C.

E 325

~ .,,

I I Gi 225 I

, I LL 125 25 0 10 20 30 40 so 60 Time (s)

---$3.00 - *- $4.00 -----$5.00 -$6.00 Figure 16: LCC Hot Channel Fuel Temperature Versus Time from Pulse Initiation for Several Pulse Reactivity Additions The maximum effect of initial conditions at power were evaluated by simulating the reactor operating at the maximum available reactivity with $3 reserved for th e pulsed reactivity addition (core excess at the maximum of $7). Immediately prior to pulsing operations, the hot channel element was established at 8.25 kW (corresponding to a core power of 433 kW). The maximum fuel temperature in the hot channel prior to the pulse was 252 °C, and following the pulsed insertion of $3, the peak hot channel fuel temperature was 579°C and peak power 74.4 kW (Fig. 17).

20

700 9.0E+04 8.0E+04 600 I -- - -----

u ,,I

- 7.0E+04

/

, /

--3...:

0 /

500

..i II I

l!:! 6.0E+04

s n, 400
,n, 5.0E+04 a, a,

=t Q.

300 ~~ 4.0E+04 3 E 0


-- ~i :. ...

Q.

~ 3.0E+04 C

Qi 200 a,

s L&.
                                                                                                  • 2.0E+04 E a,

100

................... l .OE+04 w 0 O.OE+OO 60 70 80 90 100 Time (s)

- - Fuel Temperature ****

  • Power Figure 17: LCC Hot Channel Fuel Temperature and Element Power Versus Time for a $3 Pulse from Steady-State Operation with Element at an Initial Power of 8.25 kW and Fuel Temperature of 252 °C (Note that pulse was initiated at 70 seconds on the time scale shown)

A maximum pulsed reactivity addition of $3 .00 is adequate to maintain fuel element temperature less than 50% of the limit. Maximum pulsed reactivity addition with the reactor operating at the balance of excess reactivity will not exceed the limiting fuel temperature at any initial achievable power level.

4.3 Continuous Reactivity Addition Transient (Control Rod Withdrawal Event)

Annual measurement of control rod speeds support evaluation of the maximum reactivity addition rate; control rod drive speeds are typically about 30 in. per minute. A set of TRACE calculations were performed to simulate the effect of a continuous control rod withdrawal to the full out position for various integral rod worths. Reactivity addition was modeled based on the fraction of total reactivity added as a function of position, and a constant speed was assumed to determine the fraction of the total integral reactivity added as a function of time for intervals (full in to full out) of 5, 30, 45, 75, 90, 120 and 135 seconds. Scale factors of $3, $4, $5, $6 and $7 were applied to each interval. The power and time resulting from this set of calculations was modified with the hot channel peaking factor, and a time dependent power calculation was performed. The characteristic of a 5 second interval are essentially a reactor pulse with a small perturbation on the pulse-tail. Power, temperature, and reactivity characteristics for a reactivity addition to $3 over 45 seconds is displayed in Figs. 18 and 19. The CHFR (using the Bernath correlation) was calculated as a minimum of 2.41 for the $7 reactivity additions to a minimum of 5.76 for a $3 addition, both at 135 seconds (2.25 minutes) for full reactivity addition .

21

20 400 18 ,". ,,,.---------- ..J 350

/ ~/

16 l

/ ,, /

I \

" \ 300 -G....

0 Q)

~ 14

,l.,'

/ \. ....

.QJ... 12

,/ /

/

\. . . ______________________ .................................................................................... . 250 ....ttlQ) a.

3: E 0

a.. 10

\

,_,,' I/ 200 ~

QJ I ....C C

C 8 I 150 Q) ttl I E

~

6 I ~

u w

....0 *I I 100 E

c 4  :/  ::,

- -~ so E 2 *xttl

____ _] ~

0 0 0 so 100 150 200 Run Time (s)


Hot Channel Power - -Max Fuel Temp.

Figure 18: Hot Channel Power and Maximum Fuel Temperature Versus Run Time for a $3 Reactivity Addition in 45 Seconds 2.SE-02

.. 0.E+OO 2.0E-02 i ,**- ** - ** - ** - ** - **- ** - ** - ** - **- **- ** - **

\/

~

~

-2.E-06 u l.SE-02

.a "D

CII CII l.OE-02

\/

I!!

I I!

CII S.OE-03 ..

/ \

1\

a. . '

~

E O.OE+OO --

I \

\

"ii

I

-5.0E-03

' \\

\

oil \ \

C 0

\ \

~ -1.0E-02 \\

CII \\

.E \\

l:

~\ -l.E-05

~

"'CII

\

a,: -2.0E-02

-2.SE-02 m ~ ro =

Time (s) rn ~ ~ ~

-1.E-05

- *

  • 6k Add - - 6k FTC ----* 6k MTC Figure 19: Reactivity Addition, Fuel Temperature Reactivity Feedback, and Moderator Temperature Reactivity Feedback Reactivity Versus Time for a Contin uous Reactivity Addition for $3 in 45 Seconds 22

The maximum fuel temperature at $3 and $4 reactivity additions (748°C) did not vary significantly at any interval. The maximum fuel temperature for the $5 reactivity addition was 925°C for intervals from 30 seconds to 90 seconds and exceeded 950°C for intervals greater than 90 seconds (as well as all $6 and $7 reactivity additions) . Maximum fuel temperature values at $4.5 and $4.75 at 135 second intervals were tested and found to be 791 °C and 835°C, respectively.

Power level response versus time is illustrated in Figs. 20 and 21 for $3 and $7 insertions that occur over a range of intervals. As the interval time for the reactivity addition increases, the maximum power over the interval decreases.

Therefore, it was concluded that continuous complete withdrawal of control rods with an integral worth less than $4.75 at a control rod drive speed less than 0.11 in. per second (6.7 in. per minute) is adequate to maintain fuel temperature less than the maximum fuel temperature limit. Continuous full withdrawal of control rods with an integral worth less than $5 and a control rod drive speed less than 0.17 in. per second (10 in. per minute) approaches but remains below the maximum fuel temperature limit.

40000 35000 30000

!25000 ai

~ 20000 Cl/

~ 15000 Q.

10000 5000 0

0 so 100 150 Time after Initiation of Transient (s) 45 - 60 75 120 - 135 Figure 20: Power Level Versus Time After Initiation ofTransient for a Continuous Rod Withdrawal of $3 in Reactivity 23

120000 100000 80000

!ai

_,QI> 60000 QI 3

C Cl.

40000 20000 0

0 so 100 150 Time after lntiiation of Transient (s) 45 75 105 - 120 Figure 21: Power Level Versus Time After Initiation ofTransient for a Continuous Rod Withdrawal of $7 in Reactivity 4.4 LOCA Analysis The LOCA analysis is initiated with a steady-state TRACE calculation to establish initial conditions, operating at 25 kW until all temperatures are stable. A TRACE restart case was initiated as a transient calculation following the initial calculation, with fission and fission product power decay in time established using the method of ANSI/ ANS-5 .1-2014, Decay Heat Power in Light Water Reactors (as described). Four cases were calculated (table 12) using four intervals between shutdown and instantaneous replacement of water cooing with air cooling. The time-dependent behavior is shown in Fig. 22 over four hours following shutdown .

Table 12: LOSS OF WATER-COOLING ANALYSIS DELAY FOR AIR MAXIMUM COOLING (s) TEMPERATURE ( C) 0 1 709 60 699 600 663 1200 637 In a rational scenario, an automatic shutdown will be initiated before the core is voided. Drain down of pool water under the most exaggerated conditions will require on the order of 10 to 20 minutes before water cooling is secured. A 10-minute delay will result in a maximum temperature of 663°C, and a 20-minute delay will result in a maximum temperature of 637°C.

There are other practical considerations not considered in modeling that make the analysis conservative in a LOCA event. A drain-down through t he beam ports (the only path for flow) will not drain below the core, and some lower portion of the fuel elements will remain in a water environment to provide heat with conduction through the stainless-steel cladding. The air cooling will occur in extremely humid conditions, increasing heat removal capability.

24

800 700

_ 600 u

t...

~ 500

~

~ 400 a.

E

{! 300 ai

I
u. 200 QI C

~

~ 100

!C QI u 0 0 5000 10000 15000 20000 Time After Cessation of Water Cooling (s)


1 s H20 ---60 s H20 - *-600 s H20 - ** 1200 s H20 Figure 22: Maximum Post LOCA Temperatures for a 25 kW Element Versus Time Following a LOCA Event (shown for a variety of delay times for air cooling)

Analysis of fuel performance during a LOCA for the AFF RI reactor predicated on 72 hours8.333333e-4 days <br />0.02 hours <br />1.190476e-4 weeks <br />2.7396e-5 months <br /> of full power per week indicates a maximum fuel temperature of about 550°C if there is no delay before water displacement and about 475°C assuming a 15-minute delay. The UT analysis assumes equilibrium steady state analysis, about 2.3 times the power history of the AFFRI reactor, generating more decay heat.

In the event of the LOCA, fuel temperature is calculated to rise to 709°C, 75% of the limiting temperature and a margin of 241 °C to the limiting temperature, for a minimal 1 second delay between reactor shutdown and displacement of water. The LCC is adequate maintain fuel integrity unchallenged by temperature in a LOCA.

5.0

SUMMARY

AND CONCLUSION A thermal-hydraulics calculation using TRACE linked to a neutronics calculation using MCNP 6.2 was performed to verify th e safety margins available in operation of the UT TRIGA reactor limiting core configuration. There are two limits that ensure fuel integrity during steady state operations and one for pulsing. During steady-state operations a fuel temperature limit of 950°C and a CHFR limit of 2.0 applies.

During pulsing operations, a fuel temperature limit of 830°C applies.

With a limiting core configuration producing 24.3 kW in the hottest element in the core, analysis shows that the CHFR is greater than 4, and fuel temperature is 6S0°C. Therefore, the limiting core configuration does not exceed limits during steady-state operations at 1.21 MW with a large margin of safety available.

In pulsing operations to $3 from non-power conditions, th e maximum fuel temperature is calculated to be 378°C. When pulsing at power, from the maximum power level available with $3 reserved for pulsing, the 25

maximum fuel temperature is calculated to be 579°C. Both of these temperatures are well below the limit.

Therefore, a $3 pulsing limit is adequate to assure the safety limit is met by a large margin.

The maximum fuel temperature from a continuous reactivity addition event to less than $4.75 at any reactivity addition rate will not exceed 835°C. Therefore, an integral control rod worth less than $4.75 is adequate to limit fuel temperature in a continuous rod withdrawal event to the safety limit with a substantial margin. If integral control rod worth is $5 in the event, temperature will not exceed the safety limit with a minimal margin as long as control rod speed does not exceed approximately 3 times the normal control rod speed.

A loss of coolant accident after continuous full power operations to steady-state conditions will not result in fuel temperature greater than 709°C with air cooling (with t he cooling delayed by 1 second). Therefore, 1.21 MW operations ensures cooling is adequate for fuel integrity in a loss of coolant accident by a large margin.

26