errata - unt digital library/67531/metadc871301/...errata page 3.6, last line - should read and...
TRANSCRIPT
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E R R A T A
Page 3 . 6 , l a s t l i n e - s h o u l d r e a d
and p r o p a g a t e outward. A s shown i n F i g u r e 3 . 5 , t h e f u e l c e n t e r
E n g i n e e r i n g Drawing H-3-27688, F u e l P in
Appendix A - Second drawing s h o u l d b e i d e n t i f i e d a s
E n g i n e e r i n g Drawing H-3-29368, I n n e r Capsule
D i s t r - 5 - 1st Column, 1 5 t h Name s h o u l d be
J . C . Gus ta f son - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -
D i s t r - 5 - 1st Column, 38 th Name s h o u l d be
D . 0 . Sheppard (10)
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BNWL- 1368
UC-25, Metals, Ceramics
and Materials
H A Z A R D S A N A L Y S I S FOR T H E
B A T T E L L E- N O R T H W E S T
E B R - I I I T R E A T T R A N S I E N T I R R A D I A T I O N T E S T - S E R I E S
G. E. Culley
D. 0. Sheppard
FFTF Fuel Department FFTF Division
June 1970
BATTELLE MEMORIAL INSTITUTE PACIFIC NORTHWEST LABORATORIES RICHLAND, WASHINGTON 99352
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Printed in the United States of America Available from
Clearinghouse for Federal Scientific and Technical Information National Bureau of Standards, U.S. Department of Commerce
Springfield, Virginia 22151 Price: Printed Copy $3.00; Microfiche $0.65
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H A Z A R D S A N A L Y S I S FOR T H E
B A T T E L L E- N O R T H W E S T
E B R - I I / T R E A T T R A N S I E N T I R R A D I A T I O N T E S T S E R I E S
G. E. Culley and D. 0 . Sheppard
ABSTRACT
This document describes the experimental equipment used
and contains an analysis of potential hazards involved in the
EBR-II/TREAT series of transient irradiations to be conducted
in support of the Fast Flux Test Facility (FFTF) fuel develop-
ment program. Approximately sixteen transient irradiations in
TREAT will be conducted on prototypic FFTF fuel pins
previously irradiated in EBR-I1 to burnups of 10,000 and
50,000 MWd/MTM. A hazards analysis was conducted on the
maximum burnup fuel pin for both the expected and maximum
accident transient conditions.
iii
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CONTENTS
ABSTRACT . LIST OF FIGURES . . . LIST OF TABLES
1.0 INTRODUCTION . 2.0 DESCRIPTION OF EXPERIMENTAL EQUIPMENT
2.1 Fuel Pin Design . 2.2 Inner Capsule Design
2.3 Treat Capsule Design
2.4 Experiment Instrumentation . 3.0 HAZARDS ANALYSIS .
3.1 Nuclear Effects on Reactor Performance . 3.2 Experiment Response with Expected Transient . 3.3 Maximum Accident Case . 3.4 Handling of Experimental Equipment .
iii
vii
viii
1.1
2.1
2.1
2.4
2.4
2.8
3.1
3.1
3.5
3.16
3.21
3.5 Chemical Reactions . 3.23
3.6 Radiation Hazards . 3.24
3.7 Disposal of Radioactive Materials . 3.33
4.0 CONCLUSIONS . 4.1
APPENDICES
A. Engineering Drawings of Experiment Apparatus
B. Fission Gas Pressure Buildup During Steady-State Irradiation and Pressure Capability of Inner Capsule
C. Calculations for Expected Transient
D. Calculations for Maximum Accident Transient
E. Tables of Photon Production Rates and Fission Gas Concentrations
REFERENCES R-1
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L I S T O F F I G U R E S
2.1 Pre-Irradiated EBR-II/TREAT Test Fuel Pin and Capsule
2.2 EBR-II/TREAT Inner Capsule Assembly
2.3 TREAT Capsule Assembly
3.1 Radial Power Distribution in EBR-II/TREAT Fuel
3.2 Effect of EBR-II/TREAT Experiment Upon Radial Flux Distribution in TREAT
3.3 EBR-II/TREAT Fuel Model for ARGUS
3.4 TREAT Transient Number 926
3.5 EBR-II/TREAT Fuel Pin Temperature Response for TREAT Transient Number 926
3.6 Peak EBR-II/TREAT Fuel Temperatures for Expected Transient
3.7 Fission Gas Release from Mixed Oxide DFR and APO Fuel Pins
3.8 Internal Fuel Pin Pressure for Maximum and Expected Transient
3.9 Cladding Temperature Versus Time for the Maximum and Expected Transient as Calculated by ARGUS
3.10 Maximum Accident Transient for EBR-II/TREAT Tests
3.11 Peak EBR-II/TREAT Capsule Temperatures for Maximum Accident Transient
3.12 TREAT Capsule Shipping Configuration
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LIST OF T A B L E S
FTR Transient Overpower Damage Levels 1.2
PNL 1 and 2 EBR-I1 Fuel Pins for TREAT Experiments 2.3
10,000 MWd/MTM EBR-I1 Exposure Roentgens/hr 3.25
50,000 MWd/MTM EBR-I1 Exposure Roentgenslhr 3.25
Total Activity After Shutdown (Curies) 3.25
10,000 MWd/MTM EBR-I1 Exposure Fission Gas Activity (Curies) After Removal from EBR-I1 3.26
50,000 MWd/MTM EBR-I1 Exposure Fission Gas Activity (Curies) After Removal from EBR-I1 3.28
TREAT Transient Exposure Green Fuel Roentgens/hr 3.30
Total Activity After Shutdown (Curies) 3.30
Fission Gas Activity (Curies) from TREAT Transient Exposure (Green Fuel) 3.31
304 SS Activation (Based on 304 SS Concentrations) 3.34
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H A Z A R D S A N A L Y S I S F O R T H E B A T T E L L E - N O R T H W E S T
E b R - I I / T R E A T T R A N S I E N T I R R A D I A T I O N T E S T S E R I E S
1.0 I N T R O D U C T I O N
A s e r i e s of t r a n s i e n t t e s t s w i l l be conducted on p r o t o -
t y p i c FTR (Fas t Test Reactor) f u e l p i n s i n suppor t of t h e FFTF
d r i v e r f u e l development program, t o e v a l u a t e t h e p in s response
and f a i l u r e t h r e sho lds f o r t h e p o s t u l a t e d acc iden t cond i t i ons
shown i n Table 1.1. The range of t e s t i n g w i l l i nc lude t h e
t h r e sho lds between (a) t h e minor and major acc iden t s and (b)
t he major and d i s r u p t i v e acc iden t s . The t r a n s i e n t t e s t s w i l l
be designed t o produce t h e a p p r o p r i a t e degree of f u e l mel t ing
and c ladd ing temperature . The f u e l p i n response w i l l be e v a l -
ua t ed t o determine i f they meet p l a n t s a f e t y c r i t e r i a . This
e v a l u a t i o n in format ion w i l l be used i n t h e s a f e t y a n a l y s i s
r e p o r t s r equ i r ed f o r c o n s t r u c t i o n and ope ra t i on of t h e FFTF.
The o v e r a l l BNW-FFTF t r a n s i e n t t e s t i n g program inc ludes
both p r e - i r r a d i a t e d and n o n i r r a d i a t e d f u e l p i n s .
P r e - i r r a d i a t e d p i n s w i l l have been i r r a d i a t e d i n e i t h e r GETR
o r E B R - 1 1 . GETR-irradiated p in s c l o s e l y approximate t h e F T R ' s
f u e l l eng th whi le EBR-11- i r radia ted p in s (13-1/2 i n . f u e l
column), more c l o s e l y approximate burnup i n t h e FTR1s neu t ron
f l u x spectrum.
The EBR-II/TREAT t e s t s e r i e s concern only t hose f u e l p in s
p r e - i r r a d i a t e d i n E B R - 1 1 . The i r r a d i a t e d , mixed-oxide f u e l
p i n s w i l l be de - encapsu l a t ed , n o n d e s t r u c t i v e l y examined, and
r e - encapsu l a t ed . The p i n s w i l l t hen be i n s e r t e d i n t o a t e s t -
ing capsu l e , t r a n s i e n t i r r a d i a t e d , and f i n a l l y nondes t ruc t i ve ly
and d e s t r u c t i v e l y examined.
The hazards a n a l y s i s p r e sen t ed f o r t h e EBR-II/TREAT
s e r i e s cons ide r s t h e t e s t f u e l p i n and t e s t cond i t i ons t h a t
w i l l produce t h e most s e v e r e r e s u l t s .
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2.0 DESCRIPTION OF EXPERIMENTAL EQUIPMENT
2.1 FUEL PIN DESIGN
The fuel pins to be transient irradiated in TREAT have
been pre-irradiated in EBR-I1 in subassemblies X031 (PNL-1)
and X032 (PNL-2). Figure 2.1 shows the fuel pin and its
sodium-bonded capsule used in EBR-11. The engineering drawing
of the fuel pin (H-3-27688) is shown in Appendix A. After the
EBR-I1 irradiation, the sodium-bonded capsule is removed, and
the fuel pin is cleaned, gamma scanned, and profilometered.
It is then re-encapsulated in an inner capsule called the
EBR-II/TREAT capsule (discussed in Section 2.2) . The fuel material is a mixed oxide composed of 25 wt%
Pu02 and 75 wt% U02 containing 93% enriched uranium. The
fuel is in the form of pressed and sintered solid and annular
pellets, 0.25 in. long, 0.212 in. in diameter, at 93% of theo-
retical density. Nominal weight of the fuel is 80 grams in a
column 13.5 in. long. Several of the fuel columns contain
axial fuel motion restrictors which are 118-in. thick
Type 304 SS wafers 0.215 in. in diameter with axial grooves on
the periphery. Fuel cladding material is Type 304 SS 0.250 in. diameter with a 0.016 in. wall thickness. Nominal fuel-to-
cladding cold diametral gap is 0.006 in. to yield a planar
smeared density of approximately 88% TD. The as-fabricated
smeared densities were somewhat less. Located directly above
the fuel column is a spring-loaded extensometer. The cladding
end closures were made by TIG welding Type 304 SS end caps in
place. The internal fuel pin atmosphere is helium plus fis-
sion gases released during steady-state irradiation. (1)
Table 2.1 shows the as-fabricated fuel parameters and steady-
state irradiation conditions for EBR-II/TREAT test fuel pins.
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FIGURE 2.1. Pre-Irradiated EBR-II/TREAT Test Fuel Pin and Capsule
i
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TABLE 2.1. PNL 1 and 2 EBR-I1 Fuel Pins for TREAT Experiments
PNL Capsule #
1-1 1-2 1-4 1-5 1-7 1-8 1-1 0 1-11
Fuel P e l l e t Densi ty, % TD
IN ALL CASES:
Fuel Smeared Density, % TD
Fuel Weight, g
78.90 80.53 77.84 78.11 76.80 77.30 72.18 72.00
Pel l e t Hole Dia., i n (Nominal )
-- -- -- --
0.054 0.054 0.054 0.054
Ax ia l Motion R e s t r i c t o r
No No Yes Yes No N 0 Yes Yes
No N 0 Yes Yes No No Yes Yes
Peak Steady Sta te Power, kW/ft
Peak Burnup MWd/MTM
8,200 7,850 8,520 8,200 8,850 8,520 8,850 9,200
Fuel Column Length, i n . 13.5 Fuel P e l l e t O.D., i n . 0.212 Fuel Cladding Dia. Gap, i n . 0.006 C l addi ng Diameter , i n . 0.250 Cladding Thickness , i n . 0.016
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2 . 2 I N N E R C A P S U L E D E S I G N
The f u e l p i n i s t o be con ta ined i n a NaK-bonded, i n s t r u -
mented capsu le a s shown i n Figure 2 . 2 . The eng ineer ing
drawing of t h i s capsu le (H-3-29368) appears i n Appendix A.
The capsu le was designed t o :
Provide an ins t rumented v e h i c l e f o r t h e p r e - i r r a d i a t e d
f u e l p i n .
Permit remote i n s e r t i o n of t h e f u e l p i n wi th subsequent
NaK f i l l i n g .
Be compatible wi th t h e e x i s t i n g BNW-TREAT capsu l e s .
The i nne r capsu l e des ign concept i s based on t h a t de s ign
proved i n t h e G.E.-PA-10 program Task C t r a n s i e n t t e s t s . (293)
The capsu l e i s cons t ruc t ed of Type 304 SS tub ing wi th a
1 - 1 /8 i n . OD and a 0.049 i n . w a l l . I t con t a in s an annula r
n i c k e l thermal dam bonded t o t h e f u e l p i n wi th e u t e c t i c NaK
a l l o y . The capsu l e i s ins t rumented w i th s i x Chromel-Alumel
thermocouples s p a t i a l l y ar ranged a s shown i n Figure 2 . 2 .
Three thermocouple h o t j unc t ions a r e l o c a t e d i n t h e NaK
annulus between t h e f u e l p i n and n i c k e l thermal dam, and t h e
o t h e r t h r e e a r e l o c a t e d i n t h e NaK annulus between t h e thermal
dam and t h e capsu le w a l l . The f u e l p i n w i l l be a t t a c h e d a t
t h e bottom, have 10 i n . of a x i a l c l ea rance and 0.090 i n . of
d i ame t r a l c l e a r a n c e i n t h e thermal dam. The o v e r a l l capsu le
l e n g t h i s 63-7/8 i n . w i t h a maximum diameter of 1 - 3 /4 i n . a t
t h e i n s t rumen ta t i on connector .
2 .3 T R E A T C A P S U L E D E S I G N
Cutaway drawing of t h e BNW-TREAT capsu l e is shown i n
Figure 2.3. This capsu le was des igned t o r e p l a c e t h e c e n t r a l
f u e l element i n TREAT and t o p rov ide an i n t e r f a c e between t h e
i n n e r capsu le and t h e TREAT r e a c t o r f o r t r a n s i e n t i r r a d i a t i o n
of mixed oxide f u e l p i n s . The capsu le c o n s i s t s o f a c y l i n -
d r i c a l p r e s s u r e v e s s e l equipped w i t h a TREAT g r ipp ing f i x t u r e
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a t i t s upper end and a f u e l element guide p i n f i t t i n g a t i t s
lower end. The e x t e r i o r of t h e capsu le has t h e same dimensions
a s a TREAT d r i v e r element except t h a t t h e c e n t r a l p o r t i o n i s
round i n c ros s s e c t i o n r a t h e r t han square . The eng ineer ing
drawing of t h i s capsu le (H-3-27729) i s shown i n Appendix A.
The primary des ign c r i t e r i a f o r t h i s capsu le is t h a t a s a
t h i r d and f i n a l containment b a r r i e r i t must r e s t r a i n t h e con-
sequences of a g r o s s f a i l u r e of both t h e f u e l p i n and t h e
i n n e r capsu l e . The capsu l e i s cons t ruc t ed of 3 i n . OD by
0.250 i n . w a l l , h e a t - t r e a t e d 4130 s t e e l tube wi th welded and
h e a t - t r e a t e d 4130 s t e e l end f i t t i n g s . The welds were s u b j e c t e d
t o X-radiography and dye p e n e t r a n t t e s t i n g and t h e completed
capsu le h y d r o s t a t i c a l l y t e s t e d t o 15,000 p s i i n t e r n a l p r e s s u r e .
The i n s i d e of t h e capsu le i s l i n e d wi th g r a p h i t e t o p reven t
molten m a t e r i a l s from c o n t a c t i n g t h e p r e s s u r e v e s s e l i n t h e
case of v i o l e n t f a i l u r e of both t h e f u e l p i n and i n n e r cap-
s u l e . An e l e c t r i c h e a t i n g element thermal ly i n s u l a t e d from
t h e p r e s s u r e v e s s e l i s used t o provide t h e d e s i r e d p r e t r a n -
s i e n t temperature i n t h e t e s t capsu le . S i x thermocouples a r e .
incorpora ted i n t h e h e a t e r can t o monitor temperatures dur ing
t h e p rehea t pe r iod . A connector i s provided t o mate wi th t h e
connector on t h e i n n e r capsu l e , and e l e c t r i c a l l e ads from both
t h e h e a t e r can and inne r capsu le pass through a bulkhead s e a l e d
wi th epoxy r e s i n . The capsu le c l o s u r e c o n s i s t s of a b o l t e d
f l a n g e wi th a p r e s s u r e - a s s i s t e d , p l a t e d , metal 0 r i n g s e a l .
Operat ing exper ience w i th capsu les o f s i m i l a r de s ign has
been ob ta ined under t h e Task C t r a n s i e n t i r r a d i a t i o n s of t h e
G.E.-conducted PA-10 program which shows t h e des ign t o be
adequate f o r t h e t r a n s i e n t t e s t i n g of mixed oxide f u e l p i n s . (3)
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2 . 4 E X P E R I M E N T I N S T R U M E N T A T I O N
The instrumentation incorporated in these experiments is
provided to:
Measure and control the pre-transient temperature.
Provide a history of inner capsule temperatures during
the transient.
Measure the post- transient equilibrium temperature of the
inner capsule.
The failure of any instrumentation will not affect the test
performance or safety features; however, such a failure could
result in loss of useful information for test evaluation. The
instrumentation consists of twelve stainless steel-sheathed
Chromel-Alumel thermocouples. Six thermocouples are located
within the inner capsule and six in the heater can in such a
way that they rest against the outer surface of the inner
capsule.
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3 .0 H A Z A R D S A N A L Y S I S
N U C L E A R E F F E C T S ON R E A C T O R P E R F O R M A N C E
The nuc l ea r E f f e c t s of performing EBR-II/TREAT e x p e r i -
ments i n t h e TREAT r e a c t o r were eva lua t ed u s ing t h e computer
codes HRG, ( 4 ) BATTELLE-REVISED-THERMOS , and DTF- IV. (6)
Because t h e capsu l e des ign i s s i m i l a r t o t h e capsu les used i n
t h e G.E.-PA-10 t r a n s i e n t t e s t i n g program ( S e r i e s I 1 and I11
i n p a r t i c u l a r ( 2 , 3 ) ) , t h e i r e f f e c t upon r e a c t o r performance i s
expected t o be s i m i l a r . The knowledge ob ta ined from t h e G.E .
t e s t s can be d i r e c t l y app l i ed t o t h e E B R - I I / T R E A T s e r i e s of
t e s t s wi th a h igh degree of conf idence.
Two neu t ron energy groups were used i n t h e a n a l y s i s s i n c e
a s i g n i f i c a n t p o r t i o n of t h e power genera ted i n t h e h i g h l y
enr iched t e s t p i n i s due t o nonthermal, neutron- induced f i s -
s i o n s , a s shown i n Figure 3.1. This f i g u r e i l l u s t r a t e s t h e
r a d i a l power p r o f i l e w i t h i n t h e t e s t f u e l and shows t h a t t h e
nonthermal c o n t r i b u t i o n accounts f o r approximately 7 0 % of t h e
power generated i n t h e c e n t e r o f t h e p in .
Figure 3.2 shows the r a d i a l neu t ron f l u x p e r t u r b a t i o n i n
t h e TREAT core a t t h e a x i a l midplane caused by t h e presence of
t h e EBR-II/TREAT capsu l e . The worth of t h e i nne r c o n t r o l rods
l o c a t e d a t a r a d i u s o f 44-1/2 cm i s decreased by on ly 5 % . The
o u t e r c o n t r o l rods a r e n o t s i g n i f i c a n t l y a f f e c t e d . The worth
of t h e E B R - I I / T R E A T capsu le a s compared t o a s t anda rd d r i v e r
element was c a l c u l a t e d t o be - 2 . 7 % A K / K .
A c a l i b r a t i o n experiment u t i l i z i n g t h e EBR-II/TREAT cap-
s u l e geometry was performed i n TREAT t o determine t h e r e l a -
t i o n s h i p between t h e t e s t p i n power and t h e r e a c t o r power.
The r e s u l t s showed t h a t t h i s r a t i o i s 1.00 x W pe r cm3
of t e s t f u e l pe r wa t t of r e a c t o r power f o r n o n i r r a d i a t e d f u e l .
For t e s t p i n s i r r a d i a t e d t o 50,000 MWd/MTM i t was c a l c u l a t e d
t h a t t h i s r a t i o would be reduced by 3 % . The f u e l p i n con ta in s
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R A D I U S , c m
FIGURE 3.1. Radial Power Distribution in EBR-II/TREAT Fuel
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ac,
x 3
w a
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approximately 8 cm3 of f u e l and t h e r e f o r e produces only 0 . 0 8 %
of t h e t o t a l power generated by t h e r e a c t o r . Since t h e e x p e r i -
ment produces such a smal l p o r t i o n of t he t o t a l power and t h e
m a j o r i t y of t h e t e s t capsu le m a t e r i a l s w i l l no t undergo a
l a r g e temperature change dur ing t h e t r a n s i e n t , t h e r e i s n o t
expected t o be a s i g n i f i c a n t e f f e c t upon the temperature
c o e f f i c i e n t of r e a c t i v i t y . The e f f e c t w i l l be s i m i l a r t o t h a t
produced by t h e G . E . experiments p r ev ious ly performed over a
wide range of r e a c t o r powers.
The n a t u r e of t r a n s i e n t t e s t i n g i n t roduces t h e p o s s i b i l i t y
of t h e f u e l be ing rea r ranged w i t h i n t h e t e s t c apsu l e . (See
paragraph 3 . 3 ) . Gross mel t ing and movement of t h e f u e l under
t h e f o r c e s of g r a v i t y and f i s s i o n gas p r e s s u r e t o t h e bottom of t h e i n n e r capsu le no t only l o c a t e s t h e f u e l i n a lower worth
p o s i t i o n i n t h e r e a c t o r , bu t due t o t h e s e l f - s h i e l d i n g e f f e c t
produces a f u e l c o n f i g u r a t i o n t h a t i s worth l e s s than t h e p i n
form. I f t h i s type of f u e l movement were t o occur dur ing t h e
t r a n s i e n t i t would n o t p r e s e n t any n e u t r o n i c hazard t o t h e
r e a c t o r . The o t h e r extreme would be t h e i d e a l i z e d c o n d i t i o n
i n which a l l t h e m a t e r i a l s , and p a r t i c u l a r l y t h e f u e l , become
homogenized w i t h i n t h e i nne r capsu le w a l l from t h e me l t i ng of
a l l i n t e r n a l components. The a n a l y s i s of t h i s c o n d i t i o n
i n d i c a t e s t h a t t h e experiment worth would i n c r e a s e by 0 . 4 %
A K / K upon homogenization. The i n c r e a s e i s caused by t h e
dec rease i n f u e l d e n s i t y and a s s o c i a t e d r educ t ion i n t h e s e l f -
s h i e l d i n g e f f e c t .
Assuming a p e s s i m i s t i c mechanism whereby molten f u e l
r e l e a s e d from t h e f u e l p i n complete ly mel t s and mixes w i th t h e
n i c k e l thermal dam, a s t e p i n c r e a s e i n e f f e c t i v e r e a c t i v i t y
would occur . I f t h e homogenization were t o t ake p l a c e b e f o r e
t h e nega t ive temperature c o e f f i c i e n t could f eed back t o t h e
r e a c t o r , t h e maximum r e a c t i v i t y a v a i l a b l e would be t h e i n i t i a l
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r e a c t o r r e a c t i v i t y (1 .5% A K / K f o r t h e maximum acc iden t c a s e ( 8 ) )
p l u s t he r e a c t i v i t y upon homogenization (0 .4% AK/K) o r
1 .9% A K / K . A r e a c t i v i t y a d d i t i o n of t h i s magnitude i s w e l l
w i t h i n t h e capac i ty o f t h e TREAT r e a c t o r from the s t a n d p o i n t
of maximum co re t empera ture , peak r e a c t o r power, and i n t e -
g r a t ed power. (9)
The l i k e l i h o o d of t h e homogenization process occu r r ing i s
remote a s was demonstrated i n t h e C 2 C t r a n s i e n t t e s t i n t h e
G.E.-PA-10 program S e r i e s I1 t r a n s i e n t . When molten f u e l came
i n con tac t w i th t h e aluminum thermal dam (lower mel t ing p o i n t
and h e a t capac i ty than n i c k e l ) t h e r e was very l i t t l e mixing
of t h e f u e l and aluminum even though t h e thermal dam was p a r -
t i a l l y mel ted. (') There was some slumping and r e l o c a t i o n of
t h e molten f u e l , b u t a review of t h e r e a c t o r power ve r sus time
d a t a d i d no t r e v e a l any s i g n i f i c a n t e f f e c t s upon t h e r e a c t o r
performance.
I t i s concluded t h a t t h e n u c l e a r performance of t h e TREAT
r e a c t o r con ta in ing t h e EBR-II/TREAT capsu le w i l l no t be
adverse ly changed dur ing e i t h e r t h e expected t r a n s i e n t o r one
i n which gross f u e l r e l o c a t i o n occurs .
EXPERIMENT RESPONSE WITH EXPECTED TRANSIENT
Seve ra l t r a n s i e n t experiments a r e planned wi th va r ious
degrees of f u e l mel t ing f o r p i n s of two l e v e l s of s t e a d y s t a t e
burnups. However, t h i s d i s c u s s i o n i s concerned wi th t h e
h i g h e s t exposure p i n and t h e maximum amount of f u e l mel t ing
which w i l l produce t h e most damaging c o n d i t i o n s . The f u e l p i n
d a t a used f o r t h e c a l c u l a t i o n s a r e from p i n number PNL-2-8
which opera ted a t 9 . 8 5 kW/ft peak power and achieved
44,250 MWd/MT exposure. The p r e - i r r a d i a t i o n phys i ca l charac-
t e r i s t i c s of t h i s p i n a r e l i s t e d i n Table 2 . 1 . The p o s t -
i r r a d i a t i o n c h a r a c t e r i s t i c s were assumed from t h e d e s t r u c t i v e
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a n a l y s i s of PNL-1 f u e l p i n s i r r a d i a t e d a t t h e same c o n d i t i o n s .
The i r r a d i a t e d f u e l ( o r i g i n a l l y s o l i d p e l l e t ) was c h a r a c t e r i z e d
a s having 0 .015- in . d iamete r c e n t r a l v o i d , an 0 .080 - in . diam-
e t e r columnar g r a i n r e g i o n of 98% T D , w i t h t h e remainder o f
t h e f u e l be ing 9 3 % TD and i n c o n t a c t w i t h t h e c l a d d i n g . ( lo)
The t r a n s i e n t h e a t t r a n s f e r program ARGUS (11) developed
and modi f i ed(12) a t ANL was used t o s e l e c t a t r a n s i e n t which
would s u b j e c t t h e f u e l p i n t o t h e p o s t u l a t e d FTR t r a n s i e n t
overpower c a s e c h a r a c t e r i z e d by 50 a r e a l % f u e l me l t i ng ( i n a
p l ane normal t o t h e a x i s o f t h e f u e l p i n ) and a peak c l a d d i n g
t empera tu re of 1480 O F . This i s t h e de f i ned t h r e s h o l d between
a "major a c c i d e n t " and a " d i s r u p t i v e acc iden t" shown i n
Table 1.1. The TREAT t r a n s i e n t t hus determined was used a s t h e
"expected t r a n s i e n t " f o r t h e hazards a n a l y s i s .
I n a d d i t i o n t o t h e f u e l p i n c h a r a c t e r i s t i c s , t h e ARGUS
i n p u t used a c o n s t a n t f u e l - t o - c l a d d i n g gap c o e f f i c i e n t of
2,000 ~ t u / h r - f t ~ - ~ ~ and a p r e h e a t t empera tu re of 300 OF. The
m a t e r i a l p r o p e r t i e s i n t h e t e s t p i n and capsu l e va ry a s a
f u n c t i o n o f t empera tu re . The nodal l ayou t and m a t e r i a l r e g i o n s
used t o d e s c r i b e t h e t e s t geometry a r e shown i n F igu re 3 . 3 .
TREAT t r a n s i e n t No. 9 2 6 was found t o produce t h e d e s i r e d
r e s u l t s on t e s t p i n PNL-2-8. T r a n s i e n t No. 9 2 6 had a peak
power o f 124 MW w i t h an i n t e g r a t e d power o f 160.5 MW/sec a s
shown i n F igu re 3 . 4 .
The tempera tu re response of t h e f u e l p i n when s u b j e c t e d
t o TREAT t r a n s i e n t No. 926, a s p r e d i c t e d by ARGUS, i s shown i n
F igu re 3 .5 . The r a d i a l power p r o f i l e of t h e p i n (F igu re 3 .1)
c ause s t h e maximum f u e l t empera tu re t o f i r s t occur a t a r a d i u s
where r /ro e q u a l s approximate ly 0 .5 and p ropaga t e s inward.
I d e a l l y , t h e power p r o f i l e would be f l a t t o s i m u l a t e a f a s t
f l u x power p r o f i l e , and me l t i ng would o r i g i n a t e a t t h e c e n t e r
and p ropaga te outward. As shown i n F igure 3 . 2 , t h e f u e l c e n t e r
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No. o f Node R e g i o n R a d i u s , f t D i a m e t e r , i n . Nodes Number
1 6 .250 x 0 . 0 1 5 2 1 - 2
BNWL-1368
Q 1 2 3 4 5 6 7 8
FIGURE 3.3. EBR-II/TREAT Fuel Model for ARGUS
N i H E A T
S I N K U O C D
I 93% T .D . F U E L 98% T.D.FUEL N a K 304 S S
C A P S U L E
W A L L
C L A D
3 0 4 S S
N a K
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T I M E , s e c
FIGURE 3 . 4 . TREAT T r a n s i e n t Number 9 2 6
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t e m p e r a t u r e l a g s beh ind t h e peak f u e l t e m p e r a t u r e by s l i g h t l y
more t h a n 0 . 5 s e c . The f u e l c e n t e r remains a t t h e phase
change t e m p e r a t u r e 4900 O F f o r 7 s e c and i s assumed t o be
m e l t e d . F i g u r e 3 . 6 shows t h e maximum f u e l t e m p e r a t u r e of
5 1 7 0 O F o c c u r r i n g a t a r a d i u s of 0 .06 i n . from c e n t e r l i n e . The
ARGUS program de te rmined t h a t s l i g h t l y more t h a n 50 a r e a l %
mel t ing . can be o b t a i n e d from t h e e x p e c t e d t r a n s i e n t w i t h a
maximum c l a d d i n g t e m p e r a t u r e of 1480 O F . I t i s a n t i c i p a t e d
t h a t t h e EBR-II/TREAT t e s t w i t h t h e expec ted t r a n s i e n t w i l l
p roduce i n c i p i e n t f u e l p i n f a i l u r e , a s d e s c r i b e d i n T a b l e 1.1.
TREAT t r a n s i e n t No. 9 2 6 was o r i g i n a l l y used on t h e G . E .
t e s t C3E i n v o l v i n g a mixed o x i d e f u e l p i n i r r a d i a t e d t o
65,000 MWd/MTM w i t h t h e p r i n c i p a l d i f f e r e n c e from t h e
EBR-II/TREAT f u e l p i n s b e i n g t h a t t h e G . E . p i n had 80% n a t u r a l
U 0 2 i n s t e a d of 75% f u l l y e n r i c h e d U 0 2 i n t h e mixed o x i d e f u e l .
The t r a n s i e n t produced a 1300 O F maximum c l a d d i n g t e m p e r a t u r e ,
a 4900 O F maximum f u e l t e m p e r a t u r e and a 30 volume p e r c e n t
m e l t i n g . The c o n c l u s i o n s from t h e p o s t - t r a n s i e n t d e s t r u c t i v e
examina t ion a r e t h a t no r a d i a l d e f o r m a t i o n o r c r a c k i n g o f t h e
c l a d d i n g o c c u r r e d , a l t h o u g h t h e r e was some a x i a l movement of
t h e f u e l . (3) I n compar ison , t h e EBR-II/TREAT t e s t t o b e p e r -
formed w i t h t r a n s i e n t 9 2 6 i s e x p e c t e d t o d e v e l o p h i g h e r power
and t e m p e r a t u r e s due t o t h e h i g h e r en r i chmen t .
Because t h e t e s t c o n d i t i o n s may produce f u e l p i n f a i l u r e ,
t h i s a s p e c t was s t u d i e d a s a p a r t o f t h e h a z a r d s e v a l u a t i o n
u s i n g t h e computer code PECT-1. ( I 3 ) The code i n p u t u t i l i z e d
t h e c l a d d i n g i n t e r n a l p r e s s u r e and t e m p e r a t u r e h i s t o r y a l o n g
w i t h an assumed mode o f f a i l u r e t o p r e d i c t t h e t ime o f f u e l
p i n f a i l u r e . The i n t e r n a l f u e l p i n p r e s s u r e d u r i n g t h e t r a n -
s i e n t was de te rmined from t h e amount o f f i s s i o n gas r e l e a s e d
by t h e f u e l d u r i n g m e l t i n g and by t h e volume of t h e i n t e r n a l
v o i d . During s t e a d y - s t a t e o p e r a t i o n i t was assumed t h a t t h e
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E B R - I I I T R E A T T R A N S I E N T
F U E L M A X I M U M T E N P E R A T U R E
FIGURE 3.6. Peak EBR-II/TREAT Fuel Temperatures for Expected Transient
550C
5000-
4500-
4000- LL 0 - 3 5 0 0- W CZ 2
2 3 0 0 0- cx U n z
2 5 0 0- I-
2 0 0 0
1 5 0 0
1 0 0 0
5 0 0
0
5 5 % M E L T-
-
- F U E L C L A D D I N G -
-
I I I I I h
0 . 0 2 0 . 0 4 0 . 0 6 0 . 0 8 0 . 1 0 0 . 1 2
R A D I U S , i n .
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PNL-2-8 f u e l r e l e a s e d 80% o f t h e g e n e r a t e d f i s s i o n gas t o t h e
plenum, based on d a t a c o n t a i n e d i n F i g u r e 3 . 7 . The r emain ing
f i s s i o n gas e n t r a p p e d i n t h e f u e l was assumed t o be r e l e a s e d
when t h e f u e l t e m p e r a t u r e r e a c h e d t h e m e l t i n g p o i n t d u r i n g t h e
t r a n s i e n t . The f u e l vapor p r e s s u r e was i g n o r e d s i n c e t h e f u e l
r e a c h e s a maximum t e m p e r a t u r e of o n l y 5170 OF, and t h e G.E
S e r i e s I1 t e s t s de te rmined t h a t f u e l vapor p r e s s u r e h a s a n
i n s i g n i f i c a n t c o n t r i b u t i o n t o p i n f a i l u r e . ( 2 ) The gas
r e l e a s e d d u r i n g t h e t r a n s i e n t was n o t a l lowed t o expand i n t o
t h e plenum b u t was c o n t a i n e d i n t h e v o i d w i t h i n t h e f u e l .
T h i s volume was based on t h e p l a n a r smeared d e n s i t y o f t h e
f u e l p i n , t h e d i f f e r e n t i a l t he rma l expans ion between t h e f u e l
and t h e c l a d d i n g , and t h e volume i n c r e a s e upon m e l t i n g . (See
Appendix C f o r d e t a i l e d c a l c u l a t i o n s . )
The i n t e r n a l f u e l p i n p r e s s u r e - t i m e r e l a t i o n s h i p i s
shown i n F i g u r e 3 . 8 , and t h e c l a d d i n g t e m p e r a t u r e r e s p o n s e i s
shown i n F i g u r e 3 .9 f o r t h e e x p e c t e d t r a n s i e n t . Cladding
f a i l u r e was assumed t o o c c u r when t h e c r o s s s e c t i o n o f t h e
c l a d d i n g a t t h e a x i a l peak power p o i n t on t h e f u e l p i n becomes
p l a s t i c t h r o u g h o u t . The PECT-1 a n a l y s i s p r e d i c t e d f u e l p i n
f a i l u r e a t 3 .50 s e c i n t o t h e t r a n s i e n t . The e f f e c t i v e
p l a s t i c d i a m e t r a l s t r a i n a t f a i l u r e was c a l c u l a t e d t o b e 0 . 2 %
a t t h e o u t e r s u r f a c e . T h i s compares w i t h b u r s t t e s t d a t a o f
c l a d d i n g s e c t i o n s from s i b l i n g PNL-1 f u e l p i n s which e x h i b i t e d
f a i l u r e s t r a i n s between 0 .2 and 1 8 . 4 % . ( 1 4 )
Assuming f a i l u r e o c c u r s a t t h a t p o i n t , 7 7 % o f t h e t r a n -
s i e n t w i l l have been comple ted , and t h e r ema in ing 23% w i l l
g e n e r a t e 29 Btu i n t h e f u e l a f t e r t h e p i n h a s f a i l e d .
Assuming t h a t a l l t h e h e a t g i v e n up by t h e f u e l i s i n s t a n t l y
used t o v a p o r i z e NaK i n t h e i n n e r c a p s u l e , a maximum p r e s s u r e
o f 3210 p s i w i l l be g e n e r a t e d w i t h i n t h e i n n e r c a p s u l e . T h i s
i s l e s s t h a n t h e c a l c u l a t e d 5500 p s i con ta inmen t c a p a b i l i t y
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T I V E , s e c
-
FIGURE 3.8. Internal Fuel Pin Pressure for Maximum and Expected Transient
-
-
-
P I N F A I L U R E - A S P R E DI C T E D -1 BY P E C T - 1
-
- MAX I MUM
T R A N S 1 E N T
P I N F A I L U R E
T R A N S I E N T
I I
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of t h e i n n e r c a p s u l e . Assumptions and c a l c u l a t i o n s a r e shown
i n Appendix C . B u r s t t e s t s conducted on i n n e r c a p s u l e s p e c i -
mens ( i n c l u d i n g weld j o i n t s ) have n o t been f o r m a l l y documented
b u t have demons t ra t ed i n t e r n a l p r e s s u r e c a p a b i l i t i e s g r e a t e r
t h a n 6 0 0 0 p s i a t room t e m p e r a t u r e . (15)
I t i s concluded t h a t by u s i n g p e s s i m i s t i c v a l u e s f o r t h e
f u e l p i n v o i d volume and e x p e c t e d s t r a i n t o f a i l u r e , t h e f u e l
p i n w i l l f a i l d u r i n g t h e expec ted t r a n s i e n t and t h e i n n e r
c a p s u l e w i l l c o n t a i n t h e consequences of t h e p i n f a i l u r e .
3 . 3 M A X I M U M A C C I D E N T C A S E
A s p r e v i o u s l y n o t e d , normal conduct o f t h e exper imen t may
induce f a i l u r e o f t h e f u e l p i n c l a d d i n g b u t s h o u l d n o t c a u s e
f a i l u r e o f t h e i n n e r c a p s u l e . I n o r d e r t o b e t t e r e v a l u a t e t h e
t e s t assembly c a p a b i l i t i e s , more ext reme c o n d i t i o n s were pos -
t u l a t e d and a n a l y z e d . A maximum a c c i d e n t t r a n s i e n t r e s u l t i n g
from a r e a c t i v i t y i n s e r t i o n 0 .3% A K / K g r e a t e r t h a n i n t e n d e d
was p r o v i d e d by TREAT p e r s o n n e l . (8 )
T h i s maximum t r a n s i e n t , shown i n F i g u r e 3 . 1 0 , h a s a peak
power o f 510 MW w i t h a n i n t e g r a t e d power o f 345 MW/sec. The
t e s t p i n r e s p o n s e t o t h i s t r a n s i e n t was e v a l u a t e d w i t h t h e
ARGUS computer code , u s i n g t h e same f u e l model and h e a t t r a n s -
f e r a s sumpt ions a s was used i n S e c t i o n 3 .2 f o r t h e e x p e c t e d
t r a n s i e n t . F i g u r e 3 . 1 1 shows t h e maximum t e m p e r a t u r e s c a l c u -
l a t e d i n t h e c a p s u l e , assuming t h a t f u e l p i n i n t e g r i t y i s main-
t a i n e d . Conclus ions were t h a t t h e f u e l p i n c l a d d i n g w i l l
f a i l from e x c e s s i v e i n t e r n a l p r e s s u r e b e f o r e it c o u l d m e l t ,
and PECT-1 was used t o de te rmine when t h e f a i l u r e would t a k e
p l a c e .
The i n t e r n a l p r e s s u r e h i s t o r y f o r t h e f u e l p i n d u r i n g t h e
maximum t r a n s i e n t was c a l c u l a t e d u s i n g t h e same assumpt ions a s
i n S e c t i o n 3 . 2 . F i g u r e 3 . 8 shows t h e i n c r e a s e i n i n t e r n a l
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0 0.1 0 . 2 0 . 3 0 . 4 0 . 5
C A P S U L E R A D I U S , in.
FIGURE 3.11. Peak EBR-II/TREAT Capsule Temperatures for Maximum Accident Transient
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p r e s s u r e w i t h t i m e , and F i g u r e 3.9 shows t h e a s s o c i a t e d c l a d -
d i n g t e m p e r a t u r e h i s t o r y . Sample c a l c u l a t i o n s a r e c o n t a i n e d
i n Appendix D .
PECT-1 p r e d i c t e d f a i l u r e of t h e c l a d d i n g a t 0 . 2 % s t r a i n
2.15 s e c a f t e r i n i t i a t i o n o f t h e t r a n s i e n t , which l e a v e s 7 0 %
of t h e t r a n s i e n t power y e t t o b e g e n e r a t e d . C a l c u l a t i o n s of
t h e amount o f ene rgy r e l e a s e d by t h e f u e l (328 Btu) a f t e r
c l a d d i n g f a i l u r e a r e c o n t a i n e d i n Appendix D . Two approaches
were t a k e n t o d e s c r i b e what happens f o l l o w i n g f u e l p i n f a i l u r e .
The f i r s t approach assumes t h a t m o l t e n f u e l a t 8500 O F
i s e x p e l l e d t o t h e bot tom of t h e i n n e r c a p s u l e and v a p o r i z e s
a l l o f t h e NaK c o n t a i n e d i n t h e i n n e r c a p s u l e . V a p o r i z a t i o n
of t h e NaK r e q u i r e s 285 Btu and would cause t h e i n n e r c a p s u l e
p r e s s u r e t o i n c r e a s e t o 20,200 p s i i f i t d i d n o t f a i l . Ca l -
c u l a t i o n s and a s sumpt ions a r e d e s c r i b e d i n Appendix D . A s
e x p l a i n e d i n S e c t i o n 3 . 2 , t h e p r e s s u r e con ta inmen t c a p a b i l i t y
of t h e i n n e r c a p s u l e a t 600 OF ( w a l l t e m p e r a t u r e ) i s 5575 p s i , and v a p o r i z a t i o n o f a l l t h e NaK c o n t a i n e d w i t h i n
w i l l c a u s e r u p t u r e . I n t h i s e v e n t , a m i x t u r e of mol t en f u e l
and NaK would b e e x p e l l e d i n t o t h e TREAT c a p s u l e , c a u s i n g t h e
p r e s s u r e i n t h e c a p s u l e t o i n c r e a s e t o a maximum of 6500 p s i .
The TREAT c a p s u l e i s c a p a b l e o f c o n t a i n i n g 15 ,000 p s i and h a s
a g r a p h i t e l i n e r t o p r o t e c t t h e c a p s u l e w a l l from c o n t a c t
w i t h m o l t e n m a t e r i a l s . The con ta inmen t c a p a b i l i t i e s of t h e
TREAT c a p s u l e from t h e s t a n d p o i n t o f m i s s i l e p e n e t r a t i o n and
dynamic shock p r e s s u r e l o a d i n g were n o t a n a l y z e d h e r e s i n c e
t h e c a p s u l e and c o n d i t i o n s a r e s i m i l a r t o t h o s e used i n t h e
G . E . t e s t s . G . E . per formed t h e s e a n a l y s e s i n t h e i r S e r i e s 2 ,
3 and 5 h a z a r d s e v a l u a t i o n s ( l 6 , 1 7 ) and found t h a t t h e m i s s i l e
problem i s i n s i g n i f i c a n t and t h a t t h e dynamic shock p r e s s u r e
was w i t h i n t h e con ta inmen t c a p a b i l i t i e s o f t h e TREAT c a p s u l e .
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The second approach i s based upon a more r e a l i s t i c e v a l u -
a t i o n o f t h e p o s t - f a i l u r e p r o c e s s . T h i s approach assumes t h a t
mol t en f u e l i s d i s c h a r g e d from t h e a x i a l c e n t e r o f t h e f u e l
p i n a t t h e h o t t e s t p o i n t . A f t e r v a p o r i z i n g a l l o f t h e NaK
c o n t a i n e d i n t h e annu lus between t h e f u e l p i n and t h e t h e r m a l
dam, t h e f u e l f r e e z e s i n t h e a n n u l u s . The n i c k e l t h e r m a l dam
can conduct h e a t away from t h e f u e l - n i c k e l i n t e r f a c e f a s t e r
t h a n i t can g e t t h rough t h e f u e l . I t has been shown e x p e r i -
m e n t a l l y ( 1 8 ) t h a t when mol t en f u e l ( s t i l l p r o d u c i n g power)
comes i n c o n t a c t w i t h n i c k e l , i t s o l i d i f i e s b e f o r e a s i g n i f i -
c a n t p o r t i o n o f t h e n i c k e l m e l t s . V a p o r i z a t i o n o f a l l t h e NaK
i n t h e annu lus r e q u i r e s o n l y 15 Btu , c a u s i n g t h e i n n e r c a p s u l e
p r e s s u r e t o i n c r e a s e t o 1330 p s i , which i s w i t h i n i t s c o n t a i n -
ment c a p a b i l i t y . Assuming t h e remainder of t h e ene rgy i s
t r a n s f e r r e d t o t h e n i c k e l t h e r m a l dam, i t s t e m p e r a t u r e would
i n c r e a s e from 330 OF t o 1480 OF, w e l l below t h e 2300 OF m e l t i n g
p o i n t of n i c k e l .
There i s e x p e r i m e n t a l e v i d e n c e t o i n d i c a t e t h a t t h e
mol t en f u e l - l i q u i d m e t a l i n t e r a c t i o n does n o t r e s u l t i n t h e
ex t reme p r e s s u r e s assumed i n t h e f i r s t approach . Work p e r -
formed by I v i n s ( l 9 ) h a s shown t h a t o x i d e f u e l p i n s which under
s e v e r e t r a n s i e n t i r r a d i a t i o n e x p e l mol t en f u e l i n t o t h e l i q u i d
m e t a l bond (sodium i n t h i s c a s e ) do n o t produce ext reme p r e s -
s u r e s w i t h i n t h e c a p s u l e . The c a p s u l e s were i n s t r u m e n t e d t o
d e t e c t p r e s s u r e changes , and t h e maximum p r e s s u r e p u l s e
d e t e c t e d w h i l e pe r fo rming f i v e t e s t s was 1800 p s i . The G . E .
t e s t s a l s o showed t h a t p r e s s u r e s g e n e r a t e d f o l l o w i n g f u e l p i n
f a i l u r e a r e w i t h i n t h e con ta inmen t c a p a b i l i t i e s of t h e i n n e r
c a p s u l e . I n t h e C3C e x p e r i m e n t , where t h e f u e l t e m p e r a t u r e s
approached 6000 OF, mol t en f u e l e x p e l l e d from t h e bot tom of
t h e f u e l p i n and c o l l e c t e d i n t h e bot tom of t h e i n n e r c a p s u l e
( s i m i l a r t o t h e f i r s t approach a s s u m p t i o n ) . No ext reme
p r e s s u r e p u l s e s were measured , and t h e i n n e r c a p s u l e c o n t a i n e d
t h e consequences o f t h e f u e l p i n f a i l u r e . (3)
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I t i s concluded t h a t i n t h e c a s e o f t h e maximum a c c i d e n t
t r a n s i e n t , f u e l p i n f a i l u r e w i l l o c c u r e a r l y i n t h e t r a n s i e n t ,
and t h e i n n e r c a p s u l e w i l l r emain i n t a c t . I n t h e u n l i k e l y
e v e n t t h a t t h e i n n e r c a p s u l e were t o f a i l , t h e TREAT c a p s u l e
would be more t h a n adequa te t o c o n t a i n t h e consequences .
3 . 4 H A N D L I N G OF E X P E R I M E N T A L E O U I P M E N T
The TREAT c a p s u l e c o n t a i n i n g t h e r a d i o a c t i v e t e s t p i n
w i l l be s h i p p e d t o and from t h e TREAT f a c i l i t y i n t h e T-2
s h i p p i n g c a s k . I n o r d e r t o f a c i l i t a t e h o r i z o n t a l l o a d i n g o f
t h e c a p s u l e i n t o t h e c a s k a t BNW, a c a s k l i n e r and c a p s u l e
a l ignment clamp w i l l be used a s shown i n F i g u r e 3 .12 . T h i s
c o n f i g u r a t i o n w i l l p e r m i t b o t h h o r i z o n t a l l o a d i n g a t BNW and
v e r t i c a l h a n d l i n g a t TREAT. The a l ignment clamp remains on
t h e c a p s u l e and w i l l n o t i n t e r f e r e w i t h t h e l o a d i n g i n t o t h e
r e a c t o r . ( 8 )
While h a n d l i n g t h e c a p s u l e , c a r e s h o u l d b e t a k e n t o n o t
d r o p , bump, o r o t h e r w i s e j a r t h e a s sembly , p a r t i c u l a r l y i n t h e
l o n g i t u d i n a l d i r e c t i o n . Such m i s h a n d l i n g c o u l d c a u s e t h e
i n n e r c a p s u l e e l e c t r i c a l c o n n e c t o r t o become d i s c o n n e c t e d .
The c a p s u l e s h o u l d remain i n e i t h e r t h e h o r i z o n t a l o r v e r t i c a l
p o s i t i o n ( g r i p p i n g f i x t u r e up) and must n o t b e i n v e r t e d . The
v e r t i c a l p o s i t i o n i s recommended f o r s t o r a g e .
The chances o f damage from h a n d l i n g c a u s i n g a r a d i o a c t i v e
h a z a r d a r e remote s i n c e t h e f u e l has t r i p l e c o n t a i n m e n t .
However, damage such a s f u e l r e l o c a t i o n p r i o r t o t h e t e s t may
produce e r r a n t r e s p o n s e t o t h e t r a n s i e n t . T h e r e f o r e , b e f o r e
t h e y a r e i n s e r t e d i n t o t h e TREAT r e a c t o r , t h e c a p s u l e s w i l l be
n e u t r o n r a d i o g r a p h e d t o a s s e s s t h e c o n d i t i o n of t h e i n t e r n a l *
components.
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TREAT C a s k
A1 i g n m e n t C l a m p
TREAT C a p s u l e
C a s k L i n e r
FIGURE 3.12. TREAT Capsule Shipping Configuration
3 . 2 2
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3 . 5 C H E M I C A L R E A C T I O N S
The p o s s i b i l i t y o f d e l e t e r i o u s chemica l r e a c t i o n s between
t h e m a t e r i a l s p r e s e n t i s remote. The m a t e r i a l s t o be used i n
t h e expe r imen t do n o t r e a c t e x p l o s i v e l y , and s p e c i a l c a r e w i l l
be e x e r c i s e d t o a s s u r e t h e e l i m i n a t i o n of a i r and w a t e r vapor
which might r e a c t w i t h t h e sodium-potass ium (NaK) a l l o y .
N e i t h e r n i c k e l no r any major c o n s t i t u e n t s of s t a i n l e s s s t e e l
r e a c t t o form a l l o y s w i t h NaK. There i s no i n d i c a t i o n t h a t
t h e thermocouple i n s u l a t o r (MgO) o r t h e Thermoflex i n s u l a t i o n
w i l l be reduced by NaK.
The p o s s i b i l i t y o f v i o l e n t chemica l r e a c t i o n s between t h e
f u e l , NaK and o t h e r c a p s u l e components i s a l s o q u i t e remote .
Chemical r e a c t i o n s between U02 and sodium were found t o o c c u r
i n a s e a l e d c o n t a i n e r h e a t e d t o 850 " C w i t h an e x c e s s o f
oxygen (O/U r a t i o g r e a t e r t h a n 2) . ( 2 0 ) A s t a b l e compound,
Na3U04 was found i n c o n c e n t r a t i o n s o f o n l y 1 0 0 t o 2 0 0 ppm
i n d i c a t i n g a v e r y l i m i t e d r e a c t i o n .
U02 and Pu02 can be reduced by a l k a l i m e t a l s b u t t h e
r e a c t i o n i s n o t s i g n i f i c a n t u n l e s s t h e a l k a l i me ta l o x i d e
p r o d u c t i s removed from t h e r e a c t i o n . S i n c e t h e c a p s u l e con-
s t i t u t e s a c l o s e d sys tem w i t h no mechanism f o r removing
sodium o r p o t a s s i u m o x i d e s , t h e r e d u c t i o n p r o c e s s i s n o t con-
s i d e r e d p r o b a b l e .
Exper imen ta l ev idence t h a t no haza rdous chemica l r e a c -
t i o n s w i l l o c c u r was found i n t h e p o s t i r r a d i a t i o n examina t ion
o f t h e G . E . C 2 C e x p e r i m e n t . ('1 Molten f u e l was e x p e l l e d from
t h e f u e l p i n i n t o t h e NaK annu lus w i t h no d e t e c t a b l e chemica l r e a c t i o n s . The aluminum t h e r m a l dam was m e l t e d and a p o r t i o n
of i t found i n s i d e t h e f u e l p i n . M e t a l l o g r a p h i c examina t ion
of t h e a luminum-conta in ing s e c t i o n r e v e a l e d a d e n d r i t i c
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s t r u c t u r e i n t h e aluminum t y p i c a l of once-mol ten a l l o y mate-
r i a l s . The a s s o c i a t e d a u t o r a d i o g r a p h y d i d n o t r e v e a l any
p lu ton ium o r uranium i n t h e aluminum c o r e .
The TREAT c a p s u l e w i l l be a . r g o n - f i l l e d d u r i n g assembly t o
a p r e s s u r e o f 1 atm ( a b s o l u t e ) i n o r d e r t o minimize t h e p o s s i -
b i l i t y o f a NaK r e a c t i o n w i t h a i r i n t h e u n l i k e l y e v e n t o f
f a i l u r e o r l e a k a g e o f t h e i n n e r c a p s u l e .
3.6 R A D I A T I O N H A Z A R D S
The computer code R I B D ( ~ ~ ) was used t o c a l c u l a t e f i s s i o n
and decay p r o d u c t s , and I S O S H L D ( ~ ~ ) was used t o c a l c u l a t e
pho ton p r o d u c t i o n and dose r a t e s . C a l c u l a t i o n s were made on
t h e b a s i s o f f i r s t p r e - i r r a d i a t i n g t e s t p i n s t o exposures o f
10 ,000 and 50,000 MWd/MTM i n EBR-I1 and t h e n , a f t e r a s u b s t a n -
t i a l c o o l i n g t i m e , s u b j e c t i n g them t o a TREAT t r a n s i e n t o f
345 MW/sec.
T a b l e s 3 . 1 and 3 .2 p r e s e n t c a l c u l a t e d dose r a t e s v e r s u s
t ime a f t e r t h e EBR-I1 i r r a d i a t i o n w i t h t h e f u e l s h i e l d e d by
b o t h t h e i n n e r and TREAT c a p s u l e s . Tab le 3 . 3 shows t o t a l
c u r i e s a s a f u n c t i o n o f c o o l i n g t i m e s . Because o f t h e remote
p o s s i b i l i t y o f c a p s u l e r u p t u r e d u r i n g s h i p m e n t , f i s s i o n gas
a c t i v i t y i s p r e s e n t e d a s a f u n c t i o n of c o o l i n g t i m e f o r b o t h
e x p o s u r e s i n T a b l e s 3 .4 and 3 . 5 . F i s s i o n gas a c t i v i t y d r o p s
o f f r a p i d l y , and by t h e t ime t h e f u e l p i n i s r e - e n c a p s u l a t e d ,
most o f t h e r a d i o a c t i v e f i s s i o n gas i s o t o p e s have decayed
away.
T a b l e s 3.6 th rough 3 . 8 show t h e dose r a t e and c u r i e con-
t e n t d a t a r e s u l t i n g from a 345 MW/sec TREAT t r a n s i e n t on g r e e n
( n o n p r e - i r r a d i a t e d ) f u e l . The dose r a t e o f a p r e - i r r a d i a t e d
t r a n s i e n t t e s t c a p s u l e i s t h e n de te rmined by add ing t h e a p p r o -
p r i a t e d o s e r a t e s f o r p r e - i r r a d i a t e d and g r e e n f u e l . The
same p r o c e d u r e i s u s e d f o r t h e c u r i e c o n t e n t . The h i g h e s t
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TABLE 3.1. 1 0 , 0 0 0 MWd/MTM EBR-I1 E x p o s u r e R o e n t g e n s / h r
D i s t a n c e f r o m C e n t e r l i n e C o o l i n g ( T r e a t C a p s u l e
T i m e s ( D a y s ) S u r f a c e ) 1 . 5 i n . 6 i n . 5 f t
0 1 . 7 1 5 x l o 6 1 . 7 3 1 x l o 5 3 . 6 7 7 x l o 3
30 5 . 1 1 4 x l o 4 4 . 9 2 0 x l o 3 1 . 1 0 2 x 1 0 '
7 5 2 . 4 6 5 x l o 4 2 . 3 4 8 x l o 3 5 . 2 9 7 x l o 1
TABLE 3 . 2 . 5 0 , 0 0 0 MWd/MTM EBR-I1 E x p o s u r e R o e n t g e n s / h r
D i s t a n c e f r o m C e n t e r l i n e C o o l i n g ( T r e a t C a p s u l e
T i m e s ( D a y s ) S u r f a c e ) 1 . 5 i n . 6 i n . 5 f t
0 1 . 7 4 6 x 1 0 6 1 . 7 6 0 x 1 0 ' 3 . 7 4 3 x l o 3
TABLE 3.3. T o t a l A c t i v i t y A f t e r S h u t d o w n ( C u r i e s )
T i m e s ( ~ a ~ s ) 1 0 , 0 0 0 MWd/MTM 5 0 , 0 0 0 MWd/MTM
0 2 . 7 2 6 x l o 4 2 . 8 2 3 x l o 4
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TABLE 3.4. 10,000 MWd/MTM EBR-I1 Exposure Fission Gas Activity (Curies) After Removal from EBR-I1
I so tope & H a l f- l i f e
B r 8 2
35.5 h
B r 8 3 2.3 h
B r 84m
6 m
B r 8 4 32 m
B r 8 5 3 m
B r 86
54 s
B r 87 56 s
B r 8 8
16 s
B r 89 4.5 s
B r 90 1.6 s
To ta l
K r 8 3m
K r 8 5m
K r 8 5
Kr 8 7
K r 88
K r 89
K r 90
K r 9 1
K r 9 2
K r 9 3
K r 94
K r 95
T o t a l
1.86 h
4.6 h
10.1 y
7 5 m
2.79 h
3.1 m
34 s
9.9 s
3 s
2 s
1.4 s
s h o r t
30 days
1.767 x
75 days
1.065 x 10-l7
180 days
0.0
0.0
0.0
0.0
0.0
0.0
0.0
0.0
0.0
0.0
0.0
0 .0
0.0
2.005 x 10-I
0.0
0.0
0.0
0 .o
0.0
0.0
0.0
0.0
0.0
2.005 x lo-'
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TABLE 3.4. (contd)
I s o t o p e & H a l f - l i f e 0 30 days 75 days 180 d a y s
T o t a l 1 .931 x 1 0 1 . 6 1 ~ 1 0 3.244 x 10-I 3.932 x
Xe 131m 11.9 d 1 . 1 8 1 4.584 x 10-I 4 .271 x l o e 2 9 .791 x
Xe 133m 2.26 d 7.767 1 . 4 8 1 ~ 1.897 x l o - ' 3.455
Xe 1 4 1
2 . 3 s 5 .243 x 1 0 0.0 0 . 0 0 .0 1
Xe 142
1 . 5 s 2.254 x 1 0 0 .0 0.0 0 .0 1
Xe 143
1 . 0 s 7.227 0.0 0.0 0 .0
Xe 144 1 .0 s 4.791 x lo-' 0 .0 0.0 0 . 0
T o t a l 1.714 x 10 7.942 6.345 x 9.793 x
Grand T o t a l 5.457 x 10 2.425 x 1 0 5 . 9 2 2 ~ 1 0 - I 2 . 0 0 5 x 1 0 - ~
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TABLE 3.5. 50,000 MWd/MTM EBR-I1 Exposure Fission Gas Activity (Curies) After Removal from EBR-I1
I so tope & H a l f- l i f e
B r 82
35.5 h
B r 83 2.3 h
B r 84m 6 m
B r 34 32 m
B r 85 3 m
B r 8 6 54 s
B r 87 56 s
B r 8 8 16 s
B r 89 4.5 s
B r 90 1 .6 s
To ta l
T o t a l
1.86 h
4.6 h
1 0 . 1 y
75 m
2.79 h
3 . 1 m
34 s
9.9 s
3 s
2 s
1 .4 s
s h o r t
30 days 75 days 180 days
1.084 x lo-17 0.0
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TABLE 3.5. (contd)
I so tope & H a l f- l i f e 0 30 days 75 days 180 days
1138 5.9 s 8.438 x 10 0.0 0.0 0.0
1
1139 2.3 s 3.543 x 10 0.0 0.0 0.0 1
T o t a l 1.931 x 10 1 . 6 1 1 ~ 1 0 3.246 x 10-I 4.261 x
T o t a l 1 . 7 1 4 ~ 1 0 ~ 7.945 6.359 x 9.821 x
Grand T o t a l 5.458 x 10 2 . 5 0 5 ~ 1 0 1.376 9.677 x 10-I
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TABLE 3 .6 . TREAT T r a n s i e n t Exposure Green Fue l Roentgens/hr
0
1 hour
1 day
Cooling t imes (days)
TABLE 3.7. T o t a l A c t i v i t y A f t e r Shutdown ( C u r i e s )
Dis tance from C e n t e r l i n e -
10 days
Cooling Times A c t i v i t y
2.365 x 10 1
1 hour
5 f e e t (Treat Capsule
1.510 x 10 0
1 day 7.271 x 10-I
Sur face) - 1.5 in .
10 days 4.99 x lo-" 30 days 1.496 x
6 i n .
2.323 x 10-I 3.359
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TABLE 3.8. Fission Gas Activity (Curies) from TREAT Transient Exposure (Green ~ u e l )
I s o t o p e and Ha l f- L i f e 0 1 h o u r 1 day 1 0 d a y s
B r 8 2
B r 8 3
B r 8 4m
B r 8 4
B r 8 5
B r 86
B r 8 7
B r 88
B r 89
B r 9 0
T o t a l
K r 8 3m
K r 8 5m
K r 8 5
K r 87
K r 8 8
K r 89
K r 90
K r 9 1
K r 9 2
K r 9 3
K r 94
K r 95
K r 9 7
T o t a l
1.86 h
4.6 h
1 0 . 1 y
75 m
2.79 h
3 . 1 m
34 s
9.9 s
3 s
2 s
1.4 s
s h o r t
1 . 0 s
30 days
7 .723 x 10-l~
0 .0
0.0
0 .0
0 .0
0 .0
0 .0
0 .0
0 .0
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TABLE 3 . 8 . (contd)
0 1 hour
3.112 3.286 x
1 . 1 9 3 x 1 0 - ~ 5 . 9 9 2 x 1 0 - ~
8.121 x 8.056 x
3.073 x 10-I 1.413 x 10 0
1.690 x lo-' 3.416 x 10-I
4.934 x 10 1 4.325 x 10-l2
2.938 x 10 2 0.0
8.129 x 10 2 0.0
1.139 x 10 3 0.0
1 day 10 days 30 days I so tope and H a l f - L e
1131 8 .1 d 1132 2.3 h 1133 20.5 h 1134 52.5 m 1135 6.7 h 1136 84 s 1137 23 s 1138 5.9 s 1139 2.3 s
T o t a l
X e 131m 11.9 d
X e 133m 2.26 d
X e 133 5.3 d
X e 135m 15.6 m
X e 135 9.16 h
X e 13 7 3.8 m
X e 138 17 m
X e 139 42 s
X e 140 1 6 s
X e 141 2.3 s
X e 14 2 1 . 5 s
X e 14 3 1 .0 s
X e 144 1.0 s
T o t a l
Grand t o t a l
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l e v e l s t h a t cou ld be e n c o u n t e r e d d u r i n g t h i s s e r i e s o f t e s t s
would be f o r a PNL-2 (50,000 MWd/MTM) f u e l p i n s u b j e c t e d t o a
TREAT t r a n s i e n t 7 5 days a f t e r removal from EBR-11. PNL-2 was
removed from EBR-I1 on August 31 , 1969 and PNL-1 on
June 1 4 , 1968. The c u r i e c o n t e n t immedia te ly a f t e r t h e t r a n - 4 s i e n t would be 6 .2 x 10 c u r i e s ( i n c l u d i n g f i s s i o n g a s ) and
t h e dose r a t e a t t h e s u r f a c e o f t h e c a p s u l e would b e
1 . 2 x l o 5 R/hr .
S p e c i f i c c a l c u l a t i o n s were n o t made o f s t a i n l e s s s t e e l
a c t i v a t i o n i n E B R - 1 1 , b u t a c t i v i t y p e r cm3 o f 304 SS s t e e l was
c a l c u l a t e d f o r t h e FTR. (23 ) Using t h e s e , t o t a l a c t i v a t i o n i s
found t o be o n l y 6 6 c u r i e s f o r t h e amount o f s t a i n l e s s s t e e l
i n t h e EBR-I1 t e s t p i n c l a d d i n g , assuming s a t u r a t e d concen-
t r a t i o n o f a l l n u c l i d e s a t 0 .025 MW ( s e e Tab le 3 . 9 ) . T h i s i s
n e g l i g i b l e when compared t o t h e f i s s i o n p r o d u c t a c t i v i t y even
a t 180 days c o o l i n g t i m e . The 6 0 ~ o , however , may c o n t r i b u t e a
s i g n i f i c a n t p a r t o f t h e a c t i v i t y a t much l o n g e r t i m e s because
o f i t s l o n g h a l f - l i f e . The spec t rum o f EBR-I1 and FTR do n o t
d i f f e r enough t o change t h i s r e s u l t a p p r e c i a b l y . A l s o , t h e
FTR spec t rum i n t e n s i t y on which t h e r e s u l t s a r e based i s
about doub le t h a t o f EBR-I1 , t h u s l e n d i n g even more c o n s e r v a -
t i s m t o t h i s r e s u l t .
Appendix E c o n t a i n s s e v e r a l t a b l e s showing photon p r o -
d u c t i o n r a t e s and f i s s i o n gas c o n c e n t r a t i o n s f o r t h e
10,000 MWd/MTM, 50,000 MWd/MTM, and t h e TREAT t r a n s i e n t c a s e s .
3 . 7 D I S P O S A L O F R A D I O A C T I V E M A T E R I A L S
A l l r a d i o a c t i v e m a t e r i a l s g e n e r a t e d d u r i n g t h e s e t e s t s
w i l l be c o n t a i n e d w i t h i n t h e TREAT c a p s u l e which w i l l be
r e t u r n e d t o BNW i n t h e T-2 s h i p p i n g c a s k .
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TABLE 3.9. 304 SS Activation (Based on 304 SS Concentrations)
Nucl ide
C 0 6 0
C r 5 1
Fe 59
5 8 5 8 ~ i ( n , p ) co 5 4
5 4 ~ e ( n , p ) Mn
5 6 5 6 Fe(n ,p ) Mn
5 2 5 2 Cr (n ,p ) V
28 2 8 ~ i ( n , p ) AI
5 4 ~ e ( n , a ) 5 1 ~ r 287 d 4.9 x 10 9
6 0 ~ i ( n , p ) 6 0 ~ o 5 .2 y 1 .2 x 1 0 9
TOTAL 96.66 x l o l o dis/cm3-sec
f o r 304 SS i n E B R - I 1 ,-) 66.356 Cur ies .
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BNWL - 136 8
4 . 0 C O N C L U S I O N S
This document d i s c u s s e s t h e p o s s i b l e hazards a s s o c i a t e d
w i t h t h e expected t r a n s i e n t and maximum a c c i d e n t t r a n s i e n t f o r
a maximum exposure f u e l p i n ( 4 4 , 2 5 0 MWd/MTM). I t i s concluded
t h a t even w i t h t h e most s e v e r e response c r e d i b l e , t h e e x p e r i -
ment w i l l be con t a ined w i t h i n t h e TREAT c a p s u l e and w i l l impose
no undue hazards t o t h e t e s t i n g f a c i l i t i e s o r pe r sonne l . Th i s
document w i l l be r e f e r e n c e d a s t h e hazards a n a l y s i s f o r t h e
complete EBR-II/TREAT t r a n s i e n t t e s t s e r i e s which i n c l u d e s
f u e l p i n s and t r a n s i e n t s o f equa l o r l e s s i r r a d i a t i o n exposure .
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A P P E N D I X A
E N G I N E E R I N G D R A W I N G S OF E X P E R I M E N T A P P A R A T U S
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i.2 1
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A P P E N D I X B
F I S S I O N GAS P R E S S U R E B U I L D U P
D U R I N G S T E A D Y - S T A T E I R R A D I A T I O N A N D
P R E S S U R E C A P A B I L I T Y O F I N N E R C A P S U L E
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A P P E N D I X B
F I S S I O N G A S P R E S S U R E I N P N L 2 - 8 B E F O R E T R E A T
I R R A D I A T I O N
7 6 . 5 7 g f u e l i n PNL 2 - 8
g o f meta l = 7 6 . 5 7 ( 2 3 9 ) = 6 7 . 5 g - 271 = 6 . 7 5 x MTM
P e a k B u r n u p = 4 . 4 2 5 x l o 4 MWd/MTM A x i a l P e a k / A v e = 1 . 1 2 5
4 . 4 2 5 x 1 0 4 MWd . 6 . 7 5 x MTM = 2 . 6 5 MWd 1.125
- MTM
2 . 6 5 MWd ( 3 . 1 x l o l o f i s s i o n s ) ( l o 6 w a t t ) ( 2 4 h r ) ( 3 6 0 0 s e c ) MW
- Watt-sec d a y hr
= 7 . 1 x l o Z 1 f i s s i o n s
A s s u m i n g 2 7 % o f f i s s i o n s f o r m gas i n f a s t f l u x
7 . 1 x 1 0 2 1 f i s s i o n s ( 0 ~ 2 7 g a s a t o m s ) = 1 . 9 2 x l o 2 ' a t o m s f l s s l o n
Vo lu me = ( 1 . 9 2 x l o Z 1 a t o m s ) ( 2 . 2 4 x l o 4 cm3 /mo le )
(STP) 6 . 0 2 x l o z 3 a t o m s / m o l e
= 7 1 . 3 cm3 f i s s i o n g a s g e n e r a t e d (STP)
O n l y 8 0 % o f t h e g a s i s a c t u a l l y r e l e a s e d t h e r e f o r e
V STP = 0 . 8 0 ( 7 1 . 3 ) c m 3
= 5 7 . 0 cm3
Volume o f He a t STP = 7 . 1 cm3
C o m b i n e d v o l u m e = 5 7 . 0 + 7 . 1 = 6 4 . 1 c m 3 (STP) Assume p r e - t r a n s i e n t t e m p e r a t u r e o f 3 0 0 OF
P 2 = '1 '1 T2 = ( 1 a t m ) ( 6 4 . 1 c m 3 ) ( 4 6 0 + 3 0 0 ) OR T1 v2 60 + 3 2 ) " R (7 . lcm3)
= 1 3 . 9 atm
= 2 0 4 p s i % I n i t i a l f u e l p i n p r e s s u r e
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P R E S S U R E C A P A B I L I T Y O F I N N E R C A P S U L E
E s t i m a t e s o f t h e i n t e r n a l p r e s s u r e c a p a b i l i t y o f t h e
i n n e r c a p s u l e a r e based on hoop s t r e s s e q u a t i o n .
Y i e l d p r e s s u r e
2 o u t - B u r s t p r e s s u r e Pb - ---h
where O Y
= y i e l d s t r e n g t h
a, = u l t i m a t e s t r e n g t h
t = 0 . 0 4 9 ' i n . d = 1 .125 i n .
Temperature o f t h e w a l l ( i n n e r s u r f a c e , wax) a t (ARGUS)
5 s e c 600 O F
10 s e c 1000 O F
a t , 600 O F ay = 23,000 p s i : (17,000-27,000)
au = 64,000 p s i : (60 ,000-67,000)
a t 1000 OF a = 23,000 p s i : (17 ,000-28,000) (BNW 891) Y
a, = 58,000 p s i : (54,000-62,000)
600 O F Py = 2004 p s i
Pb = 5 5 7 5 p s i
1 0 0 0 OF Py = 2004 p s i
Pb = 5052 p s i
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A P P E N D I X C
C A L C U L A T I O N S F O R E X P E C T E D T R A N S I E N T
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A P P E N D I X C
I N T E R N A L F U E L P I N P R E S S U R E DUE T O F U E L M E L T I N G A N D R E T A I N E D
F I S S I O N GAS R E L E A S E D U R I N G E X P E C T E D T R A N S I E N T
B A S I S :
1. N e g l i g i b l e f i s s i o n gas i s produced du r ing t r a n s i e n t
i r r a d i a t i o n .
2 . F i s s i o n gas r e t e n t i o n du r ing s t e a d y s t a t e i s assumed
a s f o l l o w s : columnar g r a i n r e g i o n 0.080 i n . diam has
5% gas r e t e n t i o n , remainder has 90% of r e t e n t i o n .
3. The f i s s i o n gas r e l e a s e d du r ing s t e a d y s t a t e i s
al lowed t o e q u i l i b r a t e w i t h t h e plenum a t a l l t imes .
4 . 100% f i s s i o n gas r e t a i n e d i n t h e f u e l du r ing s t e a d y
s t a t e i s r e l e a s e d when t h e f u e l me l t s and occup ies t h e
vo id r e g i o n a s determined by t h e smeared d e n s i t y . The
t r a n s i e n t r e l e a s e d gas does n o t e q u i l i b r a t e w i t h t h e
plenum.
5 . The f u e l i s assumed mel ted when it reaches 4900 O F .
6 . A s t h e f u e l m e l t s , i t expands and reduces t h e vo id
a v a i l a b l e f o r t r a n s i e n t r e l e a s e d f i s s i o n ga se s .
Time After Nodes Melted Transient (see Figure 3.4)
3.1 None
3.2 17-19
3.3 15-19
3.4 13-19
3.5 11-19
3.6 8-19
3.7 6-19
3.8 3-19
Sample calculations for this
* 1 0 % r e l e a s e d d u r i n g m e l t
Volume of Fuel Melted (in. 3)
None
0.0575
0.0512
0.0449
0.0391
0.0323
0.0369
0.0285
table follow
Cumulative Volume of Fuel Melted (in. 3)
None
0.0575
0.1086
0.1536
0.1926
0.2249
0.2618
0.2903
Vo 1 ume of gas Released (cm3) None
7.32
6.51
5.72
4.98
4.10
0.52"
0.40*
Size of Void Available (cm3) * *
* * Assumes t h e m e l t e d f u e l volume i n c r e a s e s 1 0 % . The o t h e r f u e l e x p a n s i o n up t o 4 9 0 0 O F i s compensated f o r b y c l a d d i n g e x p a n s i o n .
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The o r i g i n a l t o t a l volume o f f u e l
V = T ~ ~ L
= 1 ~ ( 0 . 1 0 9 ) 2 ( 1 3 . 5 ) = 0.504 i n . 3
Volume o f f i s s i o n gas g e n e r a t e d i n me l t ed f u e l a t 3.2 s e c
r 0 ' 0 5 7 5 in L71.3 crn3] = 8 . 1 3 cm3
Vf = 10.504 i n . 3 I 90% i s r e l e a s e d
S i z e of v o i d a v a i l a b l e a t 3 . 1 smeared d e n s i t y = 76.57%
3 = (0.118 i n 3 ) (16 .4 a ) = 1 . 9 3 cm 3
i n . 3
S i z e o f v o i d a v a i l a b l e a t 3 .2
= 0.0575 i n . 3 = 0.943 cm 3 'melt Volume i n c r e a s e = (0.943) (0 .1 ) = 0.094 cm3
Void d e c r e a s e = 1.93-0 .094 = 1 .84 cm 3
Sample c a l c u l a t i o n o f p r e s s u r e due t o t e m p e r a t u r e i n c r e a s e o f
s t e a d y - s t a t e r e l e a s e d f i s s i o n gas a t 3 . 1 s e c
Model
1 P , V , N , ~ Plenum Phase 1: h e a t v o i d r e g i o n t o t e m p e r a t u r e
I P , V , N , T ~ Void Phase 2 : Open v a l v e between r e g i o n s and
e q u i l i b r a t e p r e s s u r e s
a d i a b a t i c a l l y
I n i t i a l t e m p e r a t u r e ( p r e - t r a n s i e n t ) o f b o t h r e g i o n s 3 0 0 O F
T o t a l i n i t i a l f i s s i o n gas volume a t STP (bo th r e g i o n s )
6 4 . 1 cm3 (Appendix B)
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Constant values
v = 5.17 cm3 R = 670.5 psia ~ m ~ / ~ - m o l e OR
Cp = 0.00274 Btu/g O F MWaVe = 25.34 g/g-mole
= 0.0694 Btu/g-mole OF
at Time 0 pressure P = 204 psi (Appendix B)
at Time 3.1:
Grams of gas in each region at 300 OF before heat up
25.23 g-mole (64'1 cm3) g-moleg 22,400 cm
3 = 0.072 g
37% in void 63% in plenum
Phase 1: TI = 4400 OF (bulk fuel temp, ARGUS)
= [(0.045g) (300 OF) + (0.027g) (4400 OF)]O.O0274B s OF = 0.363 Btu
nlT'v Phase 2: nT = v r -
0.0694B q = 0.363 Btu = [11,786 OF n' + 4400 OF nl]g-mole OF
1 0.363 Btu g-mole OF = 0.0003*3 g-mole n = 0.0694 Btu 16,186 OF - n'TIR - (0.000324 g-mole) (4860 OR) (670.5) psi cm 5
p = , r - 1.93 cm3 g-mole OR
= 547.4 psi
at Time 3.2: 11.3% fuel melts-void size reduces
T' = 4500 OF
Phase 1:
q = [(0.00285) 1340 + 0.000324(4500)]0.0694
= 0.366 Btu
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Phase 2 : nT = n l T 1 v - - [4500] [ 5 . 1 7 cm3]
v ' 1 .84 cm3
= 555 p s i
To t h i s must be added t h e p r e s s u r e due t o e n t r a p p e d f i s s i o n
gas r e l e a s e d u r i n g m e l t
'STP ' S T P ~ - (14 .7 p s i ) (7.32 cm3) (4900 + 460) O R
P = - v T ~ ~ ~ (1.84 cm3) (460 + 32) O R
= 637 p s i
T o t a l p r e s s u r e a t 3 .2 s e c 637 + 555 = 1192 p s i
Tab le o f P r e s s u r e C a l c u l a t e d a s Above
Time
P r e s s u r e Due t o Ent rapped F i s s i o n
Gas Re lease
P r e s s u r e Due t o P r e - t r a n s i e n t Released
Gas Heatup
T o t a l a s Shown i n
F i g u r e 3 . 7
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BNWL - 1 .-i. 3
P O W E R T O B E G E N E R A T E D I N F U E L A F T E R C L A D
F A I L U R E D U R I N G E X P E C T E D T R A N S I E N T
Time of f a i l u r e 3.50 s e c a f t e r i n i t i a t i o n of t r a n s i e n t .
77% o f t r a n s i e n t has passed l e a v i n g 23% o r 37 bIW-sec.
Power f a c t o r = 1.004 x w a t t s f u e l power/cm3 f u e l
p e r w a t t o f r e a c t o r power
Volume of f u e l a t f a i l u r e = 8 .23 cm5
1 .004 w a t t s f u e l power 8 .23 cm3 f u e l 37 W-sec x l o 6 x l o m 4 Q = cm3 f u e l w a t t s r e a c t o r power
Q = 3.06 x l o 4 W-sec x 948 x Btu/W-sec
= 29 Btu g e n e r a t e d i n f u e l a f t e r f a i l u r e
Heat r e l e a s e d from c o o l i n g t h e f u e l t o 4900 O F ( f r e e z i n g
p o i n t )
Q = MCpAT C~ = 0.15 B/ lbm O F
= 5 .05 Btu
T o t a l h e a t a v a i l a b l e 29 + 5 = 34 Btu
P R E S S U R E W I T H I N I N N E R C A P S U L E F R O M V A P O R I Z I N G N a K
Weight o f NaK v a p o r i z e d by 34 Btu
Heat o f v a p o r i z a t i o n
Na = 1811 B t u / l b m
K = 872 B t u / l b m
N a K compos i t ion 78% K 2 2 % Na
Weight NaK = ( 0 . 7 g ) (34 Btu) + (0 .22) (34 Btu)
872 B t u / l b m 1811 B t u / l b m
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Volume of NaK vapor at STP
Available void for vapor exp&sion 267 cm3
Pressure after expansion with final temperature 1450 O F
(vaporization temperature)
= 3,210 psi
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A P P E N D I X D
C A L C U L A T I O N S F O R M A X I M U M
A C C I D E N T T R A N S I E N T
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A P P E N D I X D
I N T E R N A L F U E L P I N PRESSURE DUE TO F U E L M E L T I N G
AND F I S S I O N GAS R E L E A S E D U R I N G MAXIMUM
A C C I D E N T T R A N S I E N T
The b a s i s f o r t h e s e c a l c u l a t i o n s a r e t h e same a s those i n
Appendix C f o r t h e expected t r a n s i e n t , and t h e c a l c u l a t i o n s
a r e t h e same.
Time After Nodes Melted Transient (see Figure 3.4)
2.10 None
2.15 19-21
2.20 14 - 24
2.25 10 - 24
2.30 5- 25
2.35 3-35 (Au)
Volume of Fuel Melted (in. 3)
None
0.065
0.239
0.078
0.104
0.018
Cumulative Volume of Fuel Melted (in. 3)
None
0.065
0.304
Volume of Fission Gas Released
(cm31
None
8.28
Size of Void
Available (cm3) * *
* 10% r e l e a s e d d u r i n g m e l t
*Qssumes t h e m e l t e d f u e l volume i n c r e a s e s 10%. The o t h e r f u e l e x p a n s i o n up t o 4 9 0 0 OF i s compensated f o r b y c l a d d i n g e x p a n s i o n .
Table o f P re s su re s Ca lcu l a t ed a s i n Appendix C
P re s su re Due t o P re s su re Due t o To ta l a s Entrapped F i s s i o n P r e t r a n s i e n t Released Shown i n
Time Gas Released Gas Heatup Figure 3 .7
2.10 0 p s i 505 p s i 505 p s i
2.15 729 625 1354
2 . 2 0 4136 7 4 2 4878
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P O W E R T O B E G E N E R A T E D I N F U E L A F T E R C L A D
F A I L U R E D U R I N G M A X I M U M A C C I D E N T T R A N S I E N T
Time of f a i l u r e = 2.15 s e c
Power t o f u e l = 270 MW-sec
Power f a c t o r 1 .004 x w a t t s f u e l power
cm3 f u e l w a t t s r e a c t o r power
Volume o f f u e l a t f a i l u r e = 8 .23 cm3
1 .004 x w a t t s f u e l power 8 .23 cm3 f u e l 270 x l o 6 W-sec Q =
cm3 f u e l w a t t s r e a c t o r power Btu = 2.235 x l o 5 W-sec x 9.48 x fiec
= 2 . 2 Btu
Heat r e l e a s e d from c o o l i n g t h e f u e l t o 4900 O F maximum
b u l k f u e l t e m p e r a t u r e 7600 O F ( f r e e z i n g p o i n t ) (ARGUS)
= 6 8 . 5 Btu
T o t a l h e a t g e n e r a t i o n 2 1 2 + 68 .5 = 280.5 Btu
P R E S S U R E W I T H I N I N N E R C A P S U L E F R O M V A P O R I Z I N G
NaK A F T E R F A I L U R E C A U S E D BY M A X I M U M A C C I D E N T
T R A N S 1 E N T
Weight o f NaK t o b e v a p o r i z e d ( a l l NaK)
' N ~ K = 0.2175 l b m
Volume o f NaK vapor
Void = 267 cm 5
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P r e s s u r e a f t e r expansion
- (14.7 p s i ) (9.45 x l o 4 ;m3)f.:.i0) ' N ~ K - 2 6 7 cm
= 2 0 , 2 0 0 p s i vapo r i z ing a l l NaK
R e s u l t a n t p r e s s u r e when a l l NaK i n annulus between t h e
f u e l p i n and t h e h e a t s i n k i s vapor ized and t h e remaining f u e l
f r e e z e s on t h e h e a t s i n k and r a i s e s t h e h e a t s i n k t empera tu re .
Weight of NaK i n annulus = 0.0143 lbm
Volume NaK vapor
= 1 ,325 p s i
F I N A L B U L K H E A T S I N K T E M P E R A T U R E I F T H E ENERGY
R E M A I N I N G A F T E R V A P O R I Z A T I O N O F T H E N a K I N T H E
A N N U L U S A S A B S O R B E D BY T H E H E A T S I N K .
Energy r e q u i r e d t o vapo r i ze 0.0143 l b NaK
X = 14 .7 Btu t o vapo r i ze t h e NaK
280.5 Btu t o t a l energy a v a i l a b l e l e s s 14 .7 Btu
absorbed i n t h e N i h e a t s i n k .
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265.8 Btu
Volume of Ni heat sink = 8.25 in.3
Initial temperature heat sink = 330 O F
'PN i = 0.103 B/lbm O F e = 0.321 lb/in3
(ARGUS)
= ( 9 7 4 + 330) O F
= 1,304 O F final Ni temperature
melting temperature of Ni = 2250 O F
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A P P E N D I X E
T A B L E S OF P H O T O N P R O D U C T I O N R A T E S
A N D F I S S I O N G A S C O N C E N T R A T I O N S
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Group
1
2
3
4
5
6
7
8
9
1 0
11
12
1 3
1 4
1 5
16
TOTAL
TABLE I. 10,000 MWd/MTM EBR-I1 Exposure
Group Average Energy
MeV
Group Production Rate; Photcns
30 days 75 days
3 . 2 7 7 ~ 1 0 ~ ~ 1 .2 46x10
180 days
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Group
1
2
3
4
5
6
7
8
9
10
11
12
1 3
14
15
16
TOTAL
TABLE 11. 5 0 , 0 0 0 MWd/MTM EBR-I1 E x p o s u r e
Group Average Energy
MeV
.15
.25
.35
.475
.65
.825
1.00
1.225
1.475
1.700
1.900
2.100
2.300
2.500
2.700
3.00
Grwp Production Rate ; Photcns
Shutdown 180 days
7.298 x 10 l3 4.167 x 10
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GROUP
TABLE 111. TREAT Transient Exposure of Green Fuel
T o t a l
Group Avg. Energy
MeV Shutdown
9.889 x 10 12
3.939 x 10 12
2.936 x 10 12
6.047 x 10 12
4.190 x 1012
6.810 x 1 0 12
9.909 x lo1' 5.436 x 1012
4.392 x 1012
1.176 x 10 12
8.033 x 1 0 11
3.366 x 10 11
6.324 x 10 11
3.513 x 1 0 11
1.106 x 1012
8.109 x 10 11
4.98 x 10 1 3
Group Produc t ion Ba te : Photons 1 Hour 1 day 1 0 days
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TABLE IV. Fission Gas Concentration (grams)
Exposure
Element 0 30 days 75 days 180 days
B r 6.563 x 6.538 x 6.533 x 6 .533 x l o m 4 K r 8.260 x 8.238 x 8.234 x 8 . 2 2 4 ~ loe3
T o t a l 9.756 x 9.647 x 9.648 x 9.656 x
50 000 I"IwD/MTM EBR-I1
Exposure
Element 0 30 days 75 days 180 days
B r 3.269 x 3.266 x 3.266 x 3.266 x loe3 K r 4.113 x 4.110 x 4.108 x 4.103 x
I 3.354 x 3.187 x 3.187 x 3.202 x
Xe 4.059 x lo-' 4.065 x lo-' 4.066 x 10-I 4.066 x lo-' T o t a l 4.838 x 10-I 4.828 x 10-I 4.829 x loe1 4.829 x 10-I
TABLE V. F i s s i o n Gas C o n c e n t r a t i o n (grams)
TREAT T r a n s i e n t Exposure
(Green F u e l )
Element 0 I hour 1 day 10 days 30 days
T o t a l 16 .095 x 5 .173 x 5.099 x 4 .616 x 4.407 x
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R E F E R E N C E S
J . E.. Hanson. Exper imen t D e s c r i p t i o n and Hazards Eva lu- a t i o n f o r t h e PNL Mixed Oxide I r r a d i a t i o n s i n EBR-11, Task A S u b t a s k I I r r a d i a t i o n s , BNWL-650. -- B a t t e Z Z e - N o r t h w e s t , R i c h l a n d , Wash ing ton , J u l y 1968.
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D . O k r e n t e t aZ. The R e a c t o r K i n e t i c s o f t h e T r a n s i e n t R e a c t o r T e s t F a c i l i t y (TREAT), ANL-61 7 4 . Argonne Nat ionaZ L a b o r a t o r y , Argonne, I Z Z i n o i s , Sep t ember 1960.
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D . F . SchoeberZe e t aZ . A Method o f C a l c u Z a t i n g T r a n s i e n t Tempera ture s i n a M u Z t i r e q i o n , A x i s y m m e t r i c , CyZindr icaZ C o n f i g u r a t i o n . The Argus Program, 1 0 8 9 / ~ ~ 2 4 8 , W r i t t e n i n F o r t r a n 11, ANL-6654. Argonne N a t i o n a l L a b o r a t o r y , Argonne, I l l i n o i s , November 1963.
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12. J . R e g i s . " M o d i f i e d ARGUS Code" d a t e d May 12 , 1969; A t t a c h m e n t t o l e t t e r from C . E . Dickerman ( A N L ) t o J . E . Hanson ( B N W ) , d a t e d may 1969 .
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t i o n i n l ' h i c k - w a l l e d C y l i n d e r s , BNWL-1171. B a t t e Z Z e - N o r t h w e s t , R i c h l a n d , W a s h i n g t o n , O c t o b e r 1969 .
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A . E . W a l t a r e t aZ. C o n s i d e r a t i o n s on t h e Use o f Fuel Mot ion R e s t r i c t o r s i n t h e FTR Fuel P i n s , BNWL-623. B a t t e l l e - N o r t h w e s t , R i c h l a n d , W a s h i n g t o n , November 1967 .
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R. T . P e p p e r , J . R. S t u b b l e s , and C . R . T o t t Z e . " C o n s t i - t u t i o n o f t h e Sodium R i c h R e g i o n o f t h e Sodium-Uranium- Oxygen S y s t e m , " A p p l . MatZ. R e s . , p . 203. O c t o b e r 1964 .
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E . T . B o u l e t t e and C . A . Mans ius . U n p u b l i s h e d Data. B a t t e l l e - N o r t h w e s t , R i c h l a n d , W a s h i n g t o n . ( P r i v a t e Commun ica t i on )
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No. o f Couies
OFFSITE
1
3 4
DISTRIBUTION
AEC Chicago P a t e n t G r o w
G . H . Lee
AEC D i v i s i o n o f R e a c t o r Development and Technology
M . Shaw, D i r e c t o r , RDT ( 5 ) A s s t D i r f o r Nuc lea r S a f e t y A n a l y s i s F, E v a l u a t i o n B r , RDT:NS A s s t Dir f o r P l a n t Engrg, RDT F a c i l i t i e s B r , RDT:PE Components B r , RDT:PE I n s t r u m e n t a t i o n 6 C o n t r o l B r , RDT:PE L i q u i d Meta l Systems B r , RDT:PE Asst D i r f o r Program A n a l y s i s , RDT Asst D i r f o r P r o j e c t Mgmt, RDT L i q u i d Meta l s P r o j e c t s B r , RDT:PM FFTF P r o j e c t Manager, RDT:PM Asst D i r f o r R e a c t o r Engrg, RDT C o n t r o l Mechanisms B r , RDT : R E Core Design B r , RDT :RE ( 2 ) Fue l E n g i n e e r i n g B r , RDT:RE ( 5 ) Fue l Handl ing B r , RDT:RE R e a c t o r V e s s e l s B r , RDT:RE Coolant Chemis t ry B r , RDT:RT Fue l Recycle B r , RDT:RT F u e l s 6 M a t e r i a l s B r , RDT:RT R e a c t o r P h y s i c s B r , RDT:RE S p e c i a l Technology B r , RDT:RT Asst D i r f o r Engrg S t a n d a r d s , RDT E B R - I 1 P r o j e c t Manager, RDT:PM
AEC D i v i s i o n of T e c h n i c a l I n f o r m a t i o n E x t e n s i o n
AEC Idaho O p e r a t i o n s O f f i c e Nuc lea r Technology D i v i s i o n
C . W . B i l l s , D i r e c t o r
AEC San F r a n c i s c o O p e r a t i o n s O f f i c e D i r e c t o r , R e a c t o r D i v i s i o n
AEC Chicago O u e r a t i o n s O f f i c e Manager
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AEC S i t e R e p r e s e n t a t i v e s
Argonne N a t i o n a l L a b o r a t o r y - CH Argonne N a t i o n a l L a b o r a t o r y - ID Atomics I n t e r n a t i o n a l Genera l E l e c t r i c Co, Sunnyvale West inghouse E l e c t r i c C o r p o r a t i o n
Argonne N a t i o n a l L a b o r a t o r y
R . A . J a r o s s LMFBR Program Off i c e N . J . Swanson EBR-I1 Experiment Manager (15) EBR-I1 l r r a d i a t i o n C o o r d i n a t o r
Atomic Power Development Assoc .
Document L i b r a r i a n
Atomics I n t e r n a t i o n a l
FFTF Program O f f i c e
Babcock 6 Wilcox Co. Atomic Energy D i v i s i o n
S . H . E s l e e c k G . B . Gar ton
Babcock 6 Wilcox Co. B o i l e r D i v i s i o n S t e r l i n g Avenue B a r b e r t o n , Ohio 44203
T . P. F a r r e l l
B e c h t e l C o r ~ o r a t i o n
J . J . Teachnor
BNW R e ~ r e s e n t a t i v e
R . M. Fleishman (ZPPR)
Combustion E n g i n e e r i n g 1000 MWe Follow-On Study
W . P. S t a k e r , P r o j e c t Manager
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1 Combustion E n g i n e e r i n g 911 West Main S t r e e t Cha t t anooga , Tennessee 37401
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W . E . B a i l y Kar l Cohen (3) R . E . Skavdahl
Genera l E l e c t r i c Company Nuc leon ics L a b o r a t o r y P.O. Box 846 P l e a s a n t o n , C a l i f o r n i a 94566
D r . H . W . A l t e r , Manager
Gulf Genera l Atomic I n c . Genera l Atomic D i v i s i o n
Idaho Nuc lea r C o r p o r a t i o n
J . A . Buckham
L i q u i d Meta l E n g i n e e r i n g C e n t e r
R . W . Dickinson
L i q u i d Meta l I n f o r m a t i o n C e n t e r
A . E . M i l l e r
Oak Ridee N a t i o n a l L a b o r a t o r v
W . 0 . Harms
D i v i s i o n of blechanical Engrg
R . She r
Un i t ed Nuc lea r C o r p o r a t i o n Research and E n g i n e e r i n g Cen te r
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15 West inghouse E l e c t r i c C o r p o r a t i o n Atomic Power O i v i s i o n Advanced Reac to r Systems
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1 AEC Chicago P a t e n t Group
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RDT A s s i s t a n t D i r e c t o r f o r P a c i f i c Northwest L a b o r a t o r i e s
L . R . Lucas T . A . Nemzek (2) A . D . Toth
AEC R ich land O p e r a t i o n s O f f i c e
J . M . S h i v l e y
B a t t e l l e Memorial I n s t i t u t e
B e c h t e l C o r p o r a t i o n
W . A . Smith (R ich land)
WADCO --
W. H . Esselman W . M . Gajewski J . M . N o r r i s B . G . Rieck
West inghouse E l e c t r i c C o r p o r a t i o n
J . D . Herb
B a t t e l l e - N o r t h w e s t
Arneson B a l l a r d Bard Batch Bement Boyd Boyd B u l l i n g t o n Brown Bunch Burgess C a b e l l ( 2 ) C a l l e n J . C a r l s o n Cawley Chand le r
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T . T . Claudson J . C . Cochran P . D . Cohn R . $4. Crawford G . E . Cu l ley (10) G . M . Dalen J . M . Davidson D . R . Doman J . F . Erben E . A . Evans T . W. Evans L . M . F inch G . L . Fox E . E . G a r r e t t V . M . Gustafson J . W . Hagan J . P . Hale J . E . Hanson (5) R . E . Harvey B . R. Hayward P . Hofman G . R . Horn L . A . Jones G . A . L a s t R . D . Legget F . J . L e i t z W . W . L i t t l e W . B. McDonald J . S. McMahon C . R . Nash C . L . Peckinpaugh L . A . Pember R . E . P e t e r s o n 0 . W . P r i e b e J . C . Richardson W . E . Roake F. H . Shade1 D . 0 . Sheppherd (10) D . E . Simpson R . J . S q u i r e s D . D . Stepnewski C . D . Swanson J . C . Tobin R . C . Walker W . E . Warden J . W . Weber
J . H. Westsik N . G . Wi t tenbrock B. Wolfe Legal - 703 Bldg Legal ROB, 2 2 1 A BNW Techn ica l In fo rmat ion ( 5 ) BNW Technica l P u b l i c a t i o n (3) FFTF F i l e (703) (10) FFTF-TPO ( 7 0 3 )