The journal of Nuclear Science and Technology - Volume 8, Number 4, December 2018

ISSN 1810-5408  
Nuclear Science  
and Technology  
Volume 8, Number 4, December 2018  
Published by  
VIETNAM ATOMIC ENERGY SOCIETY  
VIETNAM ATOMIC ENERGY INSTITUTE  
NUCLEAR SCIENCE AND TECHNOLOGY  
Volume 8, Number 4, December 2018  
Editorial Board  
Editor-in-chief  
Tran Huu Phat (VINATOM)  
Executive Editors  
Vuong Huu Tan (VARANS)  
Tran Chi Thanh (VINATOM)  
Cao Đình Thanh (VINATOM)  
Hoang Anh Tuan (VAEA)  
Editors  
Nguyen Kien Cuong (VINATOM)  
Nguyen Nhi Dien (VINATOM)  
Nguyen Thi Kim Dung (VINATOM)  
Ho Manh Dung (VINATOM)  
Nguyen Nam Giang (VINATOM)  
Trinh Van Giap (VINATOM)  
Le Ngoc Ha (108 Military Central Hospital)  
Phan Son Hai (VINATOM)  
Le Hong Khiem (IOP)  
Dao Tien Khoa (VINATOM)  
Tran Hoai Nam (Duy Tan University)  
Dang Duc Nhan (VINATOM)  
Nguyen Hao Quang (VINATOM)  
Nguyen Mong Sinh (VINATOM)  
Tran Duc Thiep (IOP)  
Dang Quang Thieu (VINATOM)  
Le Ba Thuan (VINATOM)  
Le Huy Ham (VAAS)  
Nguyen Quoc Hien (VINATOM)  
Le Van Hong (VINATOM)  
Nguyen Trung Tinh (VARANS)  
Tran Ngoc Toan (VINATOM)  
Duong Thanh Tung (VARANS)  
Nguyen Nu Hoai Vi (VARANS)  
Nguyen Tuan Khai (VINATOM)  
Pham Dinh Khang (VINATOM)  
Science Secretary  
Hoang Sy Than (VINATOM)  
....................................................................................................................................................................................................................  
Copyright: ©2008 by the Vietnam Atomic Energy Society (VAES), Vietnam Atomic Energy Institute  
(VINATOM).  
Pusblished by  
Vietnam Atomic Energy Society, 59 Ly Thuong Kiet, Hanoi, Vietnam  
Tel: 84-24-39420463 Fax: 84-24-39424133 Email: [email protected]  
Vietnam Atomic Energy Institute, 59 Ly Thuong Kiet, Hanoi, Vietnam  
Tel: 84-24-39420463 Fax: 84-24-39422625 Email: [email protected]  
....................................................................................................................................................................................................................  
Contents  
Reactivity induced transient analysis when the occurrence of leakage in the dry  
irradiation channels of the Dalat Nuclear Research Reactor  
Dau Duc Tu, Nguyen Minh Tuan, Le Vinh Vinh, Huynh Ton Nghiem, Nguyen Kien  
Cuong, Tran Quoc Duong, Bui Phuong Nam  
01  
Burnup calculation of the OECD VVER-1000 LEU benchmark assembly using  
MCNP6 and SRAC2006  
Nguyen Huu Tiep, Nguyen Thi Dung, Tran Viet Phu, Tran Vinh Thanh, Pham Nhu  
Viet Ha  
10  
20  
26  
Particle identification for neutron rich nuclei 63,65Cr from knockout reactions  
N. D. Ton, L. X. Chung1, A. Corsi, A. Gillibert, P. D. Khue, B. D. Linh, A. Obertelli  
Development of neutron survey meter using prescila neutron probe  
Luong Thi Hong, Nguyen Tien Phong, Pham Thi Bich, Nguyen Duc Huyen  
87  
Study on the removal of interferences for the determination of Sr/86Sr isotopic  
ratio in petroleum drill-hole water samples using isotope dilution – inductively  
coupled plasma mass spectrometry (ID – ICP-MS)  
Nguyen Thi Kim Dung, Thai Thi Thu Thuy  
34  
Nuclear Science and Technology, Vol.8, No. 4 (2018), pp. 01-09  
Reactivity induced transient analysis when the occurrence  
of leakage in the dry irradiation channels  
of the Dalat Nuclear Research Reactor  
Dau Duc Tu, Nguyen Minh Tuan, Le Vinh Vinh, Huynh Ton Nghiem,  
Nguyen Kien Cuong, Tran Quoc Duong, Bui Phuong Nam  
Reactor Center, Dalat Nuclear Research Institute, VINATOM  
01 Nguyen Tu Luc Str., Dalat, Lamdong, Vietnam.  
(Received 06 December 2018, accepted 28 December 2018)  
Abstract: The leakage from the reactor pool back into the dry irradiation channels due to corrosion or  
mechanics based reason is a postulated event that could occur under operating conditions of the Dalat  
nuclear research reactor (DNRR), especially the channel 7-1 which has been installed more than 30  
years. When it occurs, the air space in these channels will be occupied by the water, subsequently a  
water column will appear in fuel region. The appearance of water column considerably enhances  
medium of neutron moderation for its surrounding fuel assemblies. As a result, a positive reactivity is  
inserted in the core and this event is classified as an insertion of excess reactivity. This event needs to  
be addressed by analysis and assessment from safety point of view and the results of analysis are also  
important for updating the reactor operating procedures. This paper presents assumptions, computer  
models and the results of analysis for such event in the DNRR by using MCNP5 code (code for  
neutronics analysis) and EUREKA-2/RR code (code for transient analysis). The calculation results  
include value of reactivity insertion, change in power of reactor, as well as surface temperature of the  
hottest fuel assembly. This research contributes to updating the reactor operating procedure.  
Keywords: Dalat nuclear research reactor (DNRR), MCNP5, EUREKA-2/RR, reactivity  
insertion, transient analysis.  
wet channel), 12 beryllium rods and a neutron  
trap [1]. The fuel assemblies are VVR-M2  
I. INTRODUCTION  
A. General information  
tubular  
fuel  
assemblies  
designed  
fuel  
The Dalat reactor, which is a swimming  
pool type reactor and uses light water as  
moderator and coolant, has 500 kW thermal  
power and put into operation in March, 1984. It  
was reconstructed and upgraded from the USA  
made 250 kW TRIGA reactor. A number of  
structures from the original TRIGA reactor such  
as the aluminum tank with the surrounding  
concrete shield, four beam-ports, thermal  
column and the graphite reflector were  
remained.  
and manufactured in Russia.  
Each  
assembly consists of three coaxial annular  
tubes as well as a header and a tail. The  
outermost fuel element has a hexagonal shape  
of 32 mm in width across parallel sides and the  
other two inner ones have a circular shape of  
22 mm and 11 mm in outer diameter,  
respectively. The beryllium rods of the reactor  
have a hexagonal shape of 32 mm in width  
across its parallel sides [1].  
B. Description of dry irradiation channels  
The reactor core is currently loaded 92  
low enriched fuel (LEU) assemblies (19.75%),  
3 irradiation channels (2 dry channels and 1  
In the reactor core, there are two dry  
irradiation channels located in cells 7-1 and 13-  
©2018 Vietnam Atomic Energy Society and Vietnam Atomic Energy Institute  
REACTIVITY INDUCED TRANSIENT ANALYSIS WHEN THE OCCURRENCE OF  
…
2 and designed for neutron activation analysis  
(NAA). Their characteristics are described in  
Table I. They are vertical channels and made  
of watertight aluminum tubes. Samples for  
NAA are packaged in small plastic bags and  
then placed in a high purity polyethylene  
irradiation capsule (so-called rabbit). Finally,  
the capsules are sent to and returned from the  
channels by a pneumatic transfer system  
(PTS). At these two channels, samples are  
irradiated for a short time from 5 seconds to 5  
minutes to analyze elements by measuring  
emission ray gamma spectrum of the short-  
lived radionuclides. The PTS of channel 7-1 is  
a remote-control system located nearby the  
reactor building. The PTS of channel 13-2 is  
mainly used for fast analysis of elements. Its  
terminal station and measuring equipments are  
located in the reactor building [2]. These  
channels enter the reactor from the top surface  
of the reactor pool, pass through the pool,  
penetrate into cells 7-1 and 13-2 of the reactor  
core and terminate 25 cm from the bottom of  
the reactor core as shown in Figures 1 and 2.  
Table I. Characteristics of the dry vertical irradiation channels  
Characteristics  
Thermal neutron flux, n/cm2/s  
Channel 7-1  
Channel 13-2  
(3.8 ÷ 4.4)1012  
(3.8 ÷ 4.2)1012  
Epithermal neutron flux, n/cm2/s  
Fast neutron flux, n/cm2/s  
Loading capacity, gram  
(4.0 ÷ 4.5)1011  
(3.0 ÷ 5.0)1012  
(3.7 ÷ 4.1)1011  
(3.0 ÷ 6.0)1012  
20  
45  
20  
10  
4
5
Irradiation time (min.), sec  
Irradiation time (max.), min.  
Sample moving speed, m/s  
30  
20  
Fig. 1. Technical drawing of pneumatic transfer channel 13-2 [2]  
2
DAU DUC TU et al.  
Fig. 2. The layout of pneumatic transfer systems (PTS) [2]  
the DNRR operating procedures after 35 years  
of operation.  
C. The leakage and assumptions for the  
transient analysis  
Under normal operating conditions, the  
The main assumption selected for  
transient analysis is a small break occurring at  
one of two dry irradiation channels (channel 7-  
1 or 13-2) with diameter of 2 mm (Ø = 2 mm)  
when the reactor is operating at the nominal  
power (500 kW). This assumption was made in  
order to simulate the above mentioned leakage.  
The other physics parameters needed for the  
transient analysis are given in Table II.  
MCNP5 Monte Carlo code and ENDF/B-VII.0  
nuclear data library were used to analyze  
reactivity insertion and EUREKA-2/RR code  
was used to study the transient of core power  
and fuel surface temperature. In fact, the  
possibility of simultaneous leakage at the 2 dry  
channels is extremely low; therefore it was not  
included in this investigation.  
leakage from the reactor pool back into the  
pneumatic irradiation channels due to  
corrosion or mechanics based reasons is a  
postulated event that could occur at the DNRR.  
When it occurs, the air space in these channels  
will be occupied by the water, subsequently a  
water column will appear in fuel region. The  
appearance of water column considerably  
enhances medium of neutron moderation for its  
surrounding fuel assemblies. As a result, a  
positive reactivity is inserted in the core that  
leads to an unwanted increase in fission rate,  
reactor power and fuel temperature. The value  
and speed of reactivity insertion mainly depend  
on the leakage rate, volume and location of the  
channels, power level and coolant temperature,  
etc. This event is classified as an event of  
insertion of excess reactivity. The events of  
insertion of excess reactivity that has the most  
potential consequences as a shim rod (SR) or  
the automatic regulating rod (AR) of the  
reactor can be withdrawn with the maximum  
speed of 3.4 mm/s and 20 mm/s, respectively,  
has been analyzed and described in the safety  
analysis report (SAR) for the DNRR [2].  
However, the event presented here has not  
been analyzed in detail so far and the result of  
this analysis is important to develop and update  
II. CALCULATION MODELS  
In the investigation, the reactor core and  
its components such as fuel assemblies, control  
rods, beryllium blocks, graphite reflector, beam  
ports, thermal column, etc. were modeled  
almost as exactly as they are. Figures 3 and 4  
show in detail MCNP5 model for the core  
configuration with 92 fuel assemblies of low  
enriched fuel (LEU) and the irradiation  
channels of the DNRR [3].  
3
REACTIVITY INDUCED TRANSIENT ANALYSIS WHEN THE OCCURRENCE OF…  
Table II. Summary of the reactor and safety parameters needed for the transient analysis  
Parameters  
Values  
Power, kW  
500  
Coolant inlet temperature, oC  
Reactor kinetics parameters  
- Prompt neutron life, s  
- Delayed neutron fraction (1$)  
Temperature reactivity coefficients  
- Moderator, (ΔK/K); (293 - 400oK)  
- Fuel, (ΔK/K)/oC;  
32  
8.92510-5  
7.55110-3  
- 1.26410-2  
(293 - 400oK)  
(400 - 500oK)  
(500 - 600oK)  
- 1.8610-3  
- 1.9210-3  
- 1.5610-3  
- Void, ΔK/K % of void  
(0 - 5%)  
-0.2432  
-0.2731  
-0.3097  
(5 - 10%)  
(10 - 20%)  
Reactivity control  
- Shutdown worth, % (2 safety rods)  
4.98  
3.4  
- Maximum withdrawal speed of one shim rod,  
mm/s  
and of the regulating rod, mm/s  
Reactor protection characteristics  
- Response time to overpower scram, s  
- Response time to fast period scram, s  
Start-up range  
20  
0.16  
9.1  
6.7  
Working range  
- Drop time of control rods, s  
0.67  
Channel No.2  
Channel No.3  
Channel No.4  
Channel No.1  
Fig. 3. Cross-sectional and vertical views of the reactor modeled by MCNP5  
4
DAU DUC TU et al.  
Core center  
Channel No.7-1  
Channel No.13-2  
Channel position  
Fig. 4. Core configuration with 92 LEU fuel assemblies and the irradiation channels modeled by MCNP5  
The EUREKA-2/RR model for the  
DNRR is shown in Figure 5. The reactor core  
contains 92 fuel assemblies and they were  
divided into 5 distinct channels. Each fuel  
channel can consist of one or more fuel  
assemblies, in which fuel channel No. 1 was  
chosen as the hottest channel containing the  
hottest fuel assembly with maximum FR (radial  
power factor). The number of fuel assembly in  
each channel and FR factors taken from  
MCNP5 calculations are given in Table III.  
The axial power distribution was also taken  
from MCNP5 calculations.  
In the present model, each fuel channel  
was divided more into 10 heat slabs along with  
10 nodes as shown in Figure 5. The model uses  
a total of 54 nodes, 50 heat slabs and 59  
junctions. The junction No. 59 is declared as a  
fill junction to simulate the primary coolant  
flow (50 m3/h) passing through the reactor core  
and by pass volume as shown in Figure 5.  
Table III. The number of fuel assemblies in each channel and radial power factors  
Fuel channel No.  
The number of fuel assemblies  
Radial power factor (FR)  
1
2
3
4
5
1
1.421  
1.256  
0.932  
0.887  
0.985  
17  
18  
28  
28  
With the scenario of leaking the  
irradiation channel in reactor core, the  
equation (1) was used to calculate the water  
column height (h) depending on the time (t)  
and the parameters L, S1, S2.  
- L: Height from the center of the  
reactor core to the surface of the reactor pool  
surface  
- h: Height of water column in the  
irradiation channel (depending on the time  
since the accident started)  
2  
S1 2g  
2S2  
- S1: The section of breaking  
(1)  
h L L   
t
- S2: The section of irradiation channel  
- g: The gravity acceleration  
In which:  
5
REACTIVITY INDUCED TRANSIENT ANALYSIS WHEN THE OCCURRENCE OF…  
Fig. 5. Schematic diagram of the model prepared for EUREKA-2/RR analysis [4]  
III. RESULTS AND DISCUSSION  
library. The number of simulated events is 260  
cycles and each of 106 particles. The calculation  
The MCNP5 calculations for the DNRR  
results of reactivity insertion depending on time  
are shown in Table IV and Figures 6 and 7.  
were performed with the critical calculation  
(KCODE) and the ENDF/B-VII.0 nuclear data  
Table IV. Time-dependent reactivity insertion for the channels 7-1 and 13-2 when air occupies by water  
Time  
Reactivity of channel 7-1  
Reactivity of channel 13-2  
(second)  
(cents)  
(cents)  
1
2
3
4
5
1.62  
5.07  
7.09  
8.52  
9.63  
0.02  
0.05  
0.04  
0.06  
0.05  
0.35  
1.96  
2.90  
3.57  
4.09  
0.03  
0.05  
0.09  
0.09  
0.08  
6
DAU DUC TU et al.  
6
7
8
9
10.54  
11.31  
11.97  
12.55  
0.07  
0.07  
0.06  
0.04  
4.51  
4.87  
5.18  
5.46  
0.06  
0.05  
0.06  
0.08  
The calculation results shown in  
Figures 6 and 7 revealed that about 9.0  
seconds after the leakage occurs, the  
channels 7-1 and 13-2 will be flooded with  
water to the corresponding height on the top  
surface of the reactor core and the  
maximum reactivity insertions are 12.55 and  
5.46 cents, respectively. The reactivity  
insertion at the channel 7-1 is greater than  
the channel 13-2. This can be explained by  
the fact that the channel 7-1 is located  
closer to the center of the reactor core and  
its volume is larger than the volume of the  
channel 13-2.  
Fig. 6. Reactivity insertion versus time when water occupies the air space in the channel 7-1  
Fig. 7. Reactivity insertion versus time when water occupies the air space in the channel 13-2  
For the next step, the calculation results  
of reactivity depending on the time by MCNP5  
were introduced into the transient calculations  
using EUREKA-2/RR. The calculation results  
of the transition of power and fuel surface  
temperature for the reactor at the hottest  
channel for the cases of channel 7-1 and 13-2  
are shown in Figures 8 and 9, respectively.  
7
REACTIVITY INDUCED TRANSIENT ANALYSIS WHEN THE OCCURRENCE OF…  
The transient calculations (see Figure.  
8) show that as soon as the event occurs, the  
time to reach the power scram set point are 3  
and 8 seconds (power scram point of the  
reactor was set at 550 kW). From Figure 9, it  
is seen that after 3.4 and 8.5 seconds, the fuel  
surface temperature increases to reach to the  
channels 7-1 and 13-2, respectively. These  
temperature values are much lower than the  
design limit imposed for the transient  
conditions (the design limit of fuel surface  
temperature is 400 oC). Therefore, this type of  
transient does not cause safety concern for the  
DNRR if the reactor protection system fulfills  
its safety functions.  
o
o
maximal values (90.8 C and 92.2 C) for the  
Fig. 8. The change in reactor power  
Fig. 9. The fuel surface temperature  
dry irradiation channels 7-1 and 13-2. The  
IV. CONCLUSIONS  
results showed that approximately 9.0  
seconds after starting the event, the  
channels 7-1 and 13-2 will be flood with  
water to the height corresponding to the top  
of reactor core. The maximal values of  
This report presented the investigation  
of reactivity insertion and transient analysis  
in power and fuel surface temperature for  
the DNRR when the leakage occurs in the  
8
DAU DUC TU et al.  
reactivity insertion determined by MCNP5  
for the channels 7-1 and 13-2 were  
12.55 0.04 and 5.46 0.08 cents,  
REFERENCE  
[1]. Nuclear Research Institute, Regulations of  
operation of Dalat nuclear reactor, March 2014.  
respectively. The transient analysis by  
[2]. Nuclear Research Institute, Safety analysis  
report for the Dalat nuclear reactor, 2012.  
EUREKA-2/RR showed that the fuel surface  
o
temperature does not exceed 92.2 C that is  
[3]. MCNP - A General Monte Carlo N-Particle  
Transport Code, Version 5, April, 2003.  
o
very low compared to design limit (400 C).  
The results of this investigation are  
considered to update the operating procedures  
of the DNRR after 35 years of operation.  
[4]. EUREKA-2/RR: A Computer Code for the  
Reactivity Accident Analyses in Research  
Reactors, Private Communication.  
9
Nuclear Science and Technology, Vol.8, No. 4 (2018), pp. 10-19  
Burnup calculation of the OECD VVER-1000 LEU benchmark  
assembly using MCNP6 and SRAC2006  
Nguyen Huu Tiep*, Nguyen Thi Dung, Tran Viet Phu, Tran Vinh Thanh and Pham Nhu Viet Ha  
Institute for Nuclear Science and Technology, Vietnam Atomic Energy Institute  
179 Hoang Quoc Viet, Cau Giay, Hanoi, Vietnam  
(Received 16 November 2018, accepted 28 November 2018)  
Abstract: The present work aims to perform burnup calculation of the OECD VVER-1000 LEU (low  
enriched uranium) computational benchmark assembly using the Monte Carlo code MCNP6 and the  
deterministic code SRAC2006. The new depletion capability of MCNP6 was applied in the burnup  
calculation of the VVER-1000 LEU benchmark assembly. The OTF (on-the-fly) methodology of  
MCNP6, which involves high precision fitting of Doppler broadened cross sections over a wide  
temperature range, was utilized to handle temperature variation for heavy isotopes. The collision  
probability method based PIJ module of SRAC2006 was also used in this burnup calculation. The  
reactivity of the fuel assembly, the isotopic concentrations and the shielding effect due to the presence  
of the gadolinium isotopes were determined with burnup using MCNP6 and SRAC2006 in  
comparison with the available published benchmark data. This study is therefore expected to reveal  
the capabilities of MCNP6 and SRAC2006 in burnup calculation of VVER-1000 fuel assemblies.  
Keywords: VVER-1000 LEU fuel assembly, fuel burnup, MCNP6, SRAC2006.  
configurations. In this regard, the Experts  
Group has carried out a benchmarking effort  
called the OECD VVER-1000 LEU (low  
enriched uranium) and MOX assembly  
computational benchmark for verification of  
the Russian calculation codes and methods in  
support for the WG plutonium disposition  
mission [1]. The benchmark consists of two  
different hexagonal fuel assemblies: a uniform  
LEU fuel assembly with 12 UGD (uranium-  
gadolinium) rods and a profiled MOX fuel  
assembly with 12 UGD rods. These two  
assemblies are representative of the advanced  
designs under active R&D in Russia for  
VVER-1000 reactors and similar to the  
designs that are expected to be used in the  
plutonium disposition mission. Various  
solutions of the benchmark are reported in the  
I. INTRODUCTION  
The United States and Russian  
Federation, under a mutual agreement, have  
been working towards the final disposition of  
weapons-grade (WG) surplus plutonium in  
each country as mixed-oxide (MOX) fuel in  
existing commercial nuclear reactors. To  
support this mission, the OECD/NEA  
established an international Experts Group to  
facilitate the sharing of existing information  
and experience and to deal with the physics  
and fuel behavior of MOX fuel as it relates to  
the WG plutonium disposition. Recent work  
in Russia, where WG MOX fuel will be used  
in both fast reactor (BN-600) and light water  
reactors (VVER-1000), has focused on the  
certification of the calculation codes and the  
design of MOX fuel assemblies and core  
©2018 Vietnam Atomic Energy Society and Vietnam Atomic Energy Institute  
NGUYEN HUU TIEP et al.  
literature and they are based on different  
methodology for MCNP, which involves  
high precision fitting of Doppler broadened  
cross sections over a wide temperature  
range, will be utilized to handle temperature  
variation for heavy isotopes [14]. In  
addition, the collision probability method  
based PIJ module of SRAC2006 will also be  
utilized in the burnup calculation of the  
VVER-1000 LEU assembly. The ENDF/B-  
VII.0 nuclear data library will be used in the  
MCNP6 and SRAC2006 calculations,  
respectively. This study is therefore  
expected to reveal the capabilities of  
MCNP6 and SRAC2006 in burnup  
calculation of VVER-1000 fuel assemblies.  
calculation codes and nuclear data libraries  
[1-7]. Most of these solutions have been  
obtained by means of collision probability or  
similar methodologies, while few of them are  
based on Monte Carlo methods.  
In  
Vietnam,  
the  
reactor  
fuel  
management in general and fuel burnup  
calculation in particular have been studied for  
years, especially for the Dalat Nuclear  
Research Reactor (DNRR) [8-10]. While a  
huge experience with the fuel burnup  
calculation of the DNRR has been  
accumulated over 30 years, there are only few  
publications related to fuel burnup calculation  
for power reactors like VVER-1000. In 2016,  
Hiep et al. [11] developed an MCNP5-  
ORIGEN coupling scheme for burnup  
calculation of VVER-1000 fuel assemblies.  
The coupling scheme was verified against the  
II. CALCULATION METHODOLOGY  
The VVER-1000 LEU benchmark  
hexagonal assembly consists of 300 fuel pin  
cells with 3.7 wt% 235U, 12 UGD (Uranium-  
Gadolinium) pin cells with 3.6 wt% 235U and  
4 wt% Gd2O3, 18 water filled guide tubes for  
control rod insertion and one central water  
filled instrumentation tube. The configuration  
and main design parameters of the VVER-  
1000 LEU fuel assembly are shown in Fig. 1  
OECD  
VVER-1000  
LEU  
benchmark  
assembly [1]. However, the predictor-  
corrector method has not yet been applied in  
the scheme and this can result in potential  
errors during the burnup calculation.  
Additionally, only the cross sections for 24  
actinides and 61 fission products were used in  
this verification due to the unavailability of  
many MCNP5 cross sections.  
and Table  
I,  
respectively.  
Detailed  
information of material composition and  
geometry of fuel pins, cladding, moderator,  
UGD pins, central and guide tubes, etc. can be  
easily found in Ref. [1]. The cell numeration  
of the one-sixth of the fuel assembly for  
simulating different isotopic compositions is  
illustrated in Fig. 2.  
The present work aims at performing  
a comparative burnup analysis of the OECD  
VVER-1000 LEU computational benchmark  
assembly using the Monte Carlo code  
MCNP6 [12] and the deterministic code  
SRAC2006 [13]. The new depletion  
capability of MCNP6 will be applied in the  
burnup calculation for the VVER-1000 LEU  
The burnup calculation for the VVER-  
1000 LEU benchmark assembly under the  
hot operating poisoned condition (the S1  
state) will be performed using MCNP6 and  
assembly.  
The  
On-The-Fly  
(OTF)  
11  
BURNUP CALCULATION OF THE OECD VVER-1000 LEU BENCHMARK ASSEMBLY…  
SRAC2006. Under this condition, the fuel  
temperature is 1027 K and the moderator  
temperature is 575 K with equilibrium 135Xe  
and 149Sm concentrations and a power  
density of 108 MWt/m3 up to a burnup 40  
MWd/kgHM. In the MCNP6 and SRAC  
calculations, the UGD rods are divided into 5  
annuli of equal area as required in the  
benchmark document [1] in order to account  
for the shielding effect due to the gadolinium  
isotopes. This allows the calculation of  
nuclide concentrations as a function of the  
radial position in the UGD rods.  
However, the default nuclear data  
in MCNP6 are given at certain  
temperatures for heavy isotopes (293.6,  
600, 900, 1200 and 2500K); while the  
fuel temperature of 1027K is needed in  
this calculation. There are various  
methods to cope with such kind of  
temperature dependence [14]. One of the  
suitable methods for MCNP6 is the OTF  
methodology for fitting of Doppler  
broadened cross sections and this method  
was applied in this study. The OTF data  
for heavy isotopes in the VVER-1000  
LEU  
benchmark  
assembly  
that  
In the MCNP6 simulation, the  
statistical error of ~30 pcm was obtained as  
the neutron history of 5x106 for parallel  
depletion calculation was selected and the  
burnup calculation was performed with 160  
steps of 0.25 MWd/kgHM. MCNP6 includes  
the new depletion capability that links steady  
state flux calculations in MCNP6 and nuclide  
depletion calculations in CINDER90. A  
steady state flux calculation is run in MCNP6  
to determine the system eigenvalue, group  
fluxes, energy integrated reaction rates,  
fission multiplicity, and recoverable energy  
per fission. CINDER90 then uses these  
values generated by MCNP6 to perform  
depletion calculation to generate new number  
densities for the next time step. MCNP6  
takes the new number densities generated by  
CINDER90 for the next steady state flux  
calculation. This linked process is repeated  
until the end of the final time step. It is noted  
that CINDER90 contains transmutation data  
information for over 3400 isotopes, 1325  
fission products, yield set for 30 actinides.  
correspond to the temperature range of  
293.6 to 1200 K were created from the  
ENDF/B-VII.0 library at the temperature  
of 293.6 K.  
The PIJ module with its cell burnup  
routine of the SRAC2006 code system was  
also utilized for the burnup calculation of  
the VVER-1000 LEU benchmark assembly.  
The PIJ module that is based on the  
collision probability method was used for  
lattice cell calculations. The cell burnup  
routine used one-group collapsed flux  
distribution and the collapsed microscopic  
cross sections to solve the depletion  
equation using the Bateman’s method. The  
burnup calculation using the cell burnup  
routine of the PIJ module was performed  
with 40 steps of 0.25 MWd/kgHM followed  
by 5 steps of 1.0 MWd/kgHM and 10 steps  
of 2.5 MWd/kgHM. The 107 neutron energy  
groups based on the ENDF/B-VII.0 library  
were collapsed to four groups for use in the  
SRAC2006 calculations.  
12  
NGUYEN HUU TIEP et al.  
Fig. 1. VVER-1000 LEU benchmark assembly configuration  
Fig. 2. Cell numeration in the one-sixth of VVER-1000 LEU benchmark assembly  
Table I. Main design parameters of VVER-1000 LEU benchmark assembly.  
Parameter  
Value  
300  
Number of UO2 fuel cells  
Number of fuel cells with Gd  
Number of guide tubes  
Number of central tubes  
Fuel cell inner radius, cm  
Fuel cell outer radius, cm  
12  
18  
1
0.3860  
0.4582  
13  
BURNUP CALCULATION OF THE OECD VVER-1000 LEU BENCHMARK ASSEMBLY…  
Central tube cell inner radius, cm  
Central tube cell outer radius, cm  
Pin pitch, cm  
0.5450  
0.6323  
1.2750  
23.6  
Fuel assembly pitch, cm  
235U enrichment, wt%  
3.7  
Gd2O3 density, g/cm3  
7.4  
increases with burnup at the beginning of  
the cycle thanks to the use of Gd2O3 in the  
UGD pins for excess reactivity control. As  
the gadolinium isotopes burn out, the  
reactivity starts to decrease with burnup in  
a nearly linear manner due to the effect of  
fissile material depletion and neutron  
absorber accumulation. It was also seen  
that the effect on reactivity of the  
gadolinium burnable absorber and the time  
at which the reactivity starts to decrease  
can be well simulated by MCNP6 and  
SRAC2006.  
III. RESULTS AND DISCUSSION  
A. Infinite multiplication factor versus  
burnup  
The infinite multiplication factor (k-  
inf) of the VVER-1000 LEU benchmark  
assembly as a function of burnup was  
calculated using MCNP6 and SRAC2006. It  
was found that the k-inf results obtained  
with MCNP6 and SRAC2006 compare well  
with the benchmark mean (BM) values as  
shown in Fig. 3. The k-inf values calculated  
with MCNP6 and SRAC2006 were slightly  
different from the BM values at the first  
burnup steps and such difference became  
B. Concentration of isotopes versus burnup  
significantly  
bigger  
after  
about  
5
The variation of the concentration  
of the nuclides 235U, 236U, 238U, 239Pu,  
240Pu, 241Pu, 242Pu, 135Xe, 149Sm, 155Gd,  
157Gd in Cell 1 and Cell 24 (see Fig. 2) as  
a function of burnup was calculated using  
MCNP6 and SRAC2006 in comparison  
with the BM values as shown in Figs. 4  
and 5. It can be seen that the isotopic  
concentrations calculated by MCNP6 and  
SRAC2006 generally agree well with the  
BM values. The maximum deviations of  
the MCNP6 and SRAC2006 results with  
the BM values for Cell 1 are -7.93% for  
149Sm and 7.29% for 239Pu at the end of  
MWd/kgHM. After the gadolinium burns  
out, the k-inf value calculated by  
SRAC2006 and the BM value tend to  
approach to each other and their differences  
with that calculated by MCNP6 become  
roughly stable. The maximum differences in  
the k-inf calculated with MCNP6 and  
SRAC2006 with the BM values are 413 pcm  
and 352 pcm, respectively; whereas those  
for MCU, TVS-M, WIMS8A, HELIOS,  
MULTICELL [1], and MCNP5-ORIGEN  
[11] are 440, 400, 460, 260, 360, and 585  
pcm, respectively.  
the  
burnup  
(40  
MWd/kgHM),  
As can be seen in Fig. 3, the  
respectively.  
reactivity of the fuel assembly slightly  
14  
NGUYEN HUU TIEP et al.  
Fig. 3. Variation of k-inf of VVER-1000 LEU benchmark assembly versus burnup  
As can be seen in Fig. 5, the burnable  
absorbers 155Gd and 157Gd deplete quickly at  
the beginning burnup steps and such quick  
depletion can be simulated by both MCNP6  
and SRAC2006. In particular, 157Gd depletes  
faster than 155Gd because of its larger thermal  
neutron absorption cross section (Gd-155σa   
60,801 barn and Gd-157σa   253,939 barn at  
E=0.0253 eV). The maximum deviations of the  
MCNP6 and SRAC2006 results with the BM  
values are -53.1% and 65.14% for 157Gd at 7  
MWd/kgHM, respectively. Those maximum  
deviations are 24.13%, 14.98%, 25.62%,  
3.06% and 61.67% for MCU, TVS-M,  
WIMS8A, HELIOS and MULTICELL,  
respectively. The discrepancies of 157Gd was  
large at the first burnup values, because 157Gd  
burns out quickly in the first burnup steps and  
its concentration becomes very small, leading  
to a large uncertainty in the calculation results.  
Fig. 4. Concentration of isotopes in Cell 1 as a function of burnup  
15  
BURNUP CALCULATION OF THE OECD VVER-1000 LEU BENCHMARK ASSEMBLY…  
Fig. 5. Concentration of isotopes in Cell 24 as a function of burnup  
section as mentioned above and thus it burns  
most in the outer zone, where the thermal  
neutron flux is highest. Consequently, the  
concentration of 157Gd at the outer zone is  
very small as compared to the inner zones,  
leading to a large statistical error.  
C. Radial isotopic concentration in UGD rod  
To investigate the variation of the  
isotopic composition in the radial direction  
of the UGD rod, Cell 24 was divided in to 5  
regions to account for the shielding effect  
due to the gadolinium isotopes. The  
concentrations of 235U, 239Pu at 40  
MWd/kgHM and 155Gd và 157Gd at 2  
MWd/kgHM were calculated using MCNP6  
and SRAC2006 and compared with the BM  
values as shown in Table II. It can be seen  
that the 235U, 239Pu, and 155Gd concentrations  
versus radius calculated by MCNP6 were in  
good agreement with the BM values within  
6.35%. However, the difference in the 157Gd  
concentration calculated by MCNP6 and the  
BM values was as high as -32.45% at the  
outer zone. It is because that 157Gd has very  
large thermal neutron absorption cross  
The  
235U,  
155Gd  
and  
157Gd  
concentrations calculated by SRAC2006  
generally agreed well with the BM values.  
However, the 239Pu concentration calculated  
by SRAC2006 showed a big difference with  
the BM value for the radial fuel zone 4 of -  
24.36% as can be seen in Table II. The  
reason might be mainly due to the using of  
only four neutron energy groups for the  
lattice cell calculations with the PIJ module  
in which the spatial self-shielding effect of  
238U or any other resonant nuclide could not  
be properly taken into account.  
Table II. Isotopic composition in Cell 24 vs radius, atoms/barn*cm  
U-235 concentration vs radius in Cell 24 at 40 MWd/kgHM  
Fuel zone number  
Radius, cm  
1
2
3
4
5
0.173  
0.244  
0.299  
0.345  
0.386  
16  
NGUYEN HUU TIEP et al.  
BM  
2.193E-04  
2.135E-04  
2.277E-04  
-2.64  
2.126E-04  
2.094E-04  
2.203E-04  
-1.51  
2.053E-04  
1.998E-04  
2.116E-04  
-2.68  
1.975E-04  
1.942E-04  
2.015E-04  
-1.67  
1.879E-04  
1.818E-04  
1.889E-04  
-3.25  
MCNP6  
SRAC  
Discrepancy, % (MCNP6-BM)/BM  
Discrepancy, % (SRAC-BM)/BM  
3.85  
3.62  
3.08  
2.00  
0.56  
Pu-239 concentration vs radius in Cell 24 at 40 MWd/kgHM  
Fuel zone number  
1
2
3
4
5
Radius, cm  
0.173  
0.244  
0.299  
0.345  
0.386  
BM  
1.083E-04  
1.065E-04  
9.847E-05  
-1.66  
1.107E-04  
1.092E-04  
9.778E-05  
-1.36  
1.159E-04  
1.139E-04  
9.699E-05  
-1.73  
1.273E-04  
1.245E-04  
9.629E-05  
-2.20  
1.978E-04  
1.967E-04  
2.083E-04  
-0.56  
MCNP6  
SRAC  
Discrepancy, % (MCNP6-BM)/BM  
Discrepancy, % (SRAC-BM)/BM  
-9.07  
-11.67  
-16.31  
-24.36  
5.29  
Gd-155 concentration vs radius in Cell 24 at 2 MWd/kgHM  
Fuel zone number  
1
2
3
4
5
Radius, cm  
0.173  
0.244  
0.299  
0.345  
0.386  
BM  
1.676E-04  
1.676E-04  
1.704E-04  
0.00  
1.636E-04  
1.632E-04  
1.665E-04  
-0.24  
1.551E-04  
1.530E-04  
1.580E-04  
-1.35  
1.333E-04  
1.284E-04  
1.366E-04  
-3.68  
8.407E-05  
7.873E-05  
8.536E-05  
-6.35  
MCNP6  
SRAC  
Discrepancy, % (MCNP6-BM)/BM  
Discrepancy, % (SRAC-BM)/BM  
1.67  
1.80  
1.86  
2.44  
1.54  
Gd-157 concentration vs radius in Cell 24 at 2 MWd/kgHM  
Fuel zone number  
1
2
3
4
5
Radius, cm  
0.173  
0.244  
0.299  
0.345  
0.386  
BM  
1.502E-04  
1.489E-04  
1.519E-04  
-0.87  
1.353E-04  
1.328E-04  
1.373E-04  
-1.85  
1.074E-04  
1.003E-04  
1.087E-04  
-6.61  
5.624E-05  
4.674E-05  
5.716E-05  
-16.89  
8.722E-06  
5.892E-06  
7.697E-06  
-32.45  
MCNP6  
SRAC  
Discrepancy, % (MCNP6-BM)/BM  
Discrepancy, % (SRAC-BM)/BM  
1.15  
1.51  
1.20  
1.64  
-11.75  
collision probability method based PIJ  
module of SRAC2006 was also utilized in  
this benchmarking calculation. The reactivity  
of the fuel assembly and the concentration of  
isotopes versus burnup obtained with  
MCNP6 and SRAC2006 generally show a  
good agreement with the BM values. The  
maximum difference in the k-inf calculated  
by MCNP6 and SRAC2006 with the BM  
values was 413 pcm and 352 pcm,  
IV. CONCLUSIONS  
A comparative burnup analysis of the  
OECD VVER-1000 LEU benchmark  
assembly was performed in this study using  
the Monte Carlo code MCNP6 and the  
deterministic code SRAC2006. The new  
depletion capability of MCNP6 and the OTF  
methodology for MCNP were applied in the  
the MCNP6 calculations; whereas the  
17  
Tải về để xem bản đầy đủ
pdf 48 trang yennguyen 13920 Free
Bạn đang xem 20 trang mẫu của tài liệu "The journal of Nuclear Science and Technology - Volume 8, Number 4, December 2018", để tải tài liệu gốc về máy hãy click vào nút Download ở trên

File đính kèm:

  • pdfthe_journal_of_nuclear_science_and_technology_volume_8_numbe.pdf