SINBAD ABSTRACT NEA-1553/74
FNS Clean Experiment on Tungsten Cylindrical Assembly
1. Name of Experiment:
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FNS/JAERI Clean Benchmark Experiment on Tungsten Cylindrical Assembly (1993)
2. Purpose and Phenomena Tested:
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A tungsten cylindrical assembly (diameter = 629 mm, height = 507 mm) was
irradiated in the D-T neutron source of Fusion Neutronic Source (FNS)
facility at JAERI. Neutron spectra down to 5 keV, dosimetry reaction rates,
gamma-ray spectra and gamma-ray heating rates were measured at 3 positions
up to 380 mm inside the tungsten assembly.
3. Description of Source and Experimental Configuration:
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The experimental configuration was basically the same as those used for some
previous clean benchmark experiments like the Lithium-Oxide, Graphite, Copper,
Beryllium, Vanadium assemblies.
The Tungsten assembly was made by stacking bricks of (50.7-50.8 mm) with
thin aluminium support frame in quasi-cylindrical shape (diameter = 629 mm,
height = 507 mm). A view of the experimental assembly is shown in Fig. 1.
The tungsten is not pure, but an alloy with a small amount of nickel and
copper. The material compositions of the tungsten assembly is given in
Table 1.
The experimental assembly was located in front of the neutron source at a
distance of 200 mm from the target. The tritium-titanium target of ~3.7E11 Bq
was bombarded by a deuteron beam of 350 keV energy to produce D-T neutrons.
The number of source D-T neutrons generated during each measurement was
determined by the alpha-particle detector with an accuracy of 2~3 %.
The D-T neutron source can be roughly described as an isotropic point 14-MeV
neutron source. The source neutron spectrum and intensity, however, depend
slightly on the emission angle. The angle-dependent source characteristics
were investigated experimentally and theoretically in detail, and a source
subroutine for the Monte Carlo transport code MCNP-4 has been prepared to
simulate the source condition precisely. This routine is listed in [3]. A
comparison between the measured and calculated angular distribution is given
in Fig. 3.2.7. in [4]. As an adequate alternative to the use of the MCNP
routine it is suggested in [1] that the source spectrum of neutrons emitted
toward the 0 degree direction with respect to the deuteron beam direction can
be used for the incident neutron spectrum on the whole front surface of the
assembly. No quantitative estimation of difference between both sources could
be though found in the available literature. The 0 degree source neutron
spectrum is shown in Fig. 2, and input cards of MCNP for description of the
source spectrum are shown in the MCNP sample input file. The si1 and sp1 cards
indicate upper neutron energies of the energy bins in MeV and probabilities
in the bins, respectively. The dir and vec parameters with the sb2 card are
used for variance reduction with the source biasing method. The weight of a
source neutron specified by the wgt parameter, 1.1261, is larger than 1.0
because more D-T neutrons are emitted to the forward direction than in the
backward direction with respect to the deuteron beam direction.
The tritium target region is also a source of gamma-rays, namely, target gamma-
rays, created by interaction of the source neutrons with structural materials
of the target. Consideration of the target gamma-rays, however, is not needed
in calculations of gamma-ray heating rates because contribution of the target
gamma-ray to the measured heating rates has been already subtracted in the
experimental data. On the other hand, the target gamma-ray contribution is
involved in the measured gamma-ray spectra. The contribution at the detector
positions deep inside the experimental assemblies is negligible, representing
at most few percents, because the experimental assembly largely attenuates the
target gamma-rays. Accordingly, it is not necessary to consider the target
gamma-rays in transport calculations for the clean benchmark experiments.
Since the W assemblies were located at least 4 m from the experimental room
walls and floor, the contribution of the background neutrons and gamma-rays
coming from the room walls and floor on the measured quantities was negligibly
small.
4. Measurement System:
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Three experimental channels for insertion of detectors were set on the lateral
surface of the assembly, and detectors were placed on the central axis of the
assembly at four positions: one on the front surface and other three inside
the assembly at the depths of 76, 228 and 380 mm. The report [1] states that
the spectra measurements were performed one by one, we conclude therefore
that the other experimental channels were closed (plugged with tungsten).
The dosimetric foils were irradiated together and simultaneously in plural
detector channels.
No information on the background correction was found in the literature.
Six techniques were employed to measure neutrons and gamma-rays. The detailed
description of the experimental techniques is given in [1] (pages 5-20):
(1) 14 mm-diameter spherical NE213 liquid organic scintillator was used as
the fast (above 2 MeV) neutron spectrometer. It was inserted into the
experimental channel hole of 22 mm diameter.
Various sources of the NE213 measurement uncertainties are discussed in
[1] (page 5) and the systematic errors are summarized in Table 2.
(2) A pair of proton recoil gas proportional counters (PRC) was used to
measure neutron spectrum in the 5 keV to 1 MeV energy range. The counter
has a cylindrical shape with the outer diameter of 19 mm and the effective
length of 127 mm. The counter is inserted into an experimental hole of
21 mm in diameter with its pre-amplifier. PRC is made of type 304 stainless
steel of a thickness of 0.41 mm.
Two types of counters were used to measure neutron spectrum in a wide
energy range. Hydrogen gas at 0.5677 MPa (5.789 kgf/cm2) with 1 percent
of CH4 filled counter was used for low-energy neutrons from 3 keV to 150
keV while for the high-energy neutrons from 150 keV to 1 MeV the counter
was filled with 50-50 mixture of hydrogen and argon gases with 1.8 percent
of nitrogen at 0.6102 MPa (6.222 kgf/cm2).
Error Assessment: Possible error sources are gas pressure (number of
hydrogen atom), n-p scattering cross section, fitting error for
differentiation of recoil proton spectrum due to count statistics and
calibration of recoil proton energy. The fitting error is the largest,
~ 3-10 % above 10 keV, while the other errors are expected to be less
than 1%. Neutron spectra below 10 keV tend to become smaller due to the
uncertainty of the W-value, which is the average energy loss per ion pair.
The error due to W-value is not included in the experimental errors.
(3) Slowing down time (SDT) method for the neutron spectrum from 1 eV to 300 eV.
A BF3 gas proportional counter with an outer diameter of 14 mm and an
effective length of 99 mm, containing 96 % boron-10 (B-10) enriched BF3
gas at the pressure of 71.5 kPa, was used for neutron detection. Using the
standard thermal neutron field the effective number of B-10 atoms in the
counter was determined to be 2.18E20 +- 3 %. The counter was inserted into
one of the experimental holes of the experimental assembly.
(4) Dosimetry reaction rate of the Al-27(n,alpha)Na-24, Nb-93(n,2n)Nb-92m,
In-115(n,n’)In-115m, 186W(n,gamma)187W and Au-197(n,gamma)Au-198 reactions
were measured by the foil activation method. Table 3 provides the
characteristics for the reactions used.
Typical sample size was 10 mm in diameter and 1 mm in thickness for
activation foils except indium and gold. Indium foils had dimensions of
10 x 10 x 1 mm3. In order to minimize the self-shielding effect for the
Au-197(n,gamma) reaction, gold foils with a size of 10 x 10 x 0.001 mm3
were adopted.
Experimental Error and Uncertainty: Major sources of the error for the
reaction rate were the gamma-ray counting statistics (0.1 ~ several %)
and the detector efficiency (2 ~ 3 %). The error for sum-peak correction
was estimated less than 2 % depending on the decay mode and fraction of
multiple gamma-ray cascade. The error for the decay correction was
reflected from the error of half-life of the activity. If the half-life
was accurate, the error for the saturation factor should be less than
1 % even for the short half-life activities.
The other errors associated with foil weight, gamma-ray self-absorption,
irradiation time, cooling time and counting time were negligibly small.
The error for neutron yield was estimated to be 2 %. The overall error
for the major part of reaction rate ranged between 3 ~ 6 %. Some data
for high threshold reaction in the deep positions suffered from poor
counting statistics due to low activation rate.
(5) Prompt gamma-ray spectrum were measured by a 40 mm diameter spherical
BC537 liquid organic scintillation counter. Outer diameter of the detector
is 48 mm and length including a photomultiplier assembly is 262 mm.
Experimental uncertainty: As explained in (6) below, typical experimental
uncertainties of the gamma-ray heating rate measured by TLDs range
between 7 ~ 15 %. The gamma-ray spectra are normalized to the gamma-ray
heating rates. Uncertainties of about 10 % is introduced by the
normalization procedure. All of the rest of experimental uncertainties,
such as statistical errors, uncertainties of the response functions,
determination of source D-T neutrons and subtraction of decay gamma-rays,
are less than 5 %. Therefore, total experimental uncertainties are
approximately 15 ~ 20 %. Note that only the statistical erorrs are
included in the Table 7.
(6) Gamma-ray heating rate were measured by thermoluminescent dosimeters
(TLDs) in combination with the atomic number interpolation method.
Gamma-ray heating rates of vanadium were deduced by interpolating the
gamma-ray heating rates measured by three types of TLDs, Mg2SiO4 (MSO,
effective atomic number Zeff = 11.1), Sr2SiO4 (SSO, Zeff = 32.5) and
Ba2SiO4 (BSO, Zeff = 49.9).
Sources of error in the measured gamma-ray heating rates are as follows:
Statistical deviation of four TLDs 5 - 15 %
Number of neutrons generated 2 - 3 %
Calibration of the TLD reader 5 %
Due to the subtraction of target gamma-rays and neutron response, the
following uncertainties are to be added to the above errors according to
the quadratic propagation of error.
Response functions for neutrons 30 %
Neutron energy spectra 10 %
Target gamma-ray 20 %
Overall errors for the obtained gamma-ray heating rates of vanadium are
~ 10%, except at the positions in the front surface of the assemblies
where they are 20 ~ 25 %.
5. Description of Results and Analysis:
-----------------------------------
The measured neutron spectra by the NE213 and PRC at the depths of 76 mm,
228 mm and 380 mm are shown in Figs.3, 4 and 5, respectively. The numerical
data of the spectra measured by the NE213 and PRC are given in Tables 4 and 5,
respectively. A measurement of neutron spectra below 10 keV by the SDT method
was attempted. However, it could not be made because of too low neutron flux
in the energy range. The measured dosimetry reaction rates are shown in Table6.
The measured gamma-ray spectra at the three positions in the tungsten assembly
are shown in Figs.6, 7 and 8. The numerical data of the spectra are given in
Table 7. The Table 8 summarises the measured gamma-ray heating rates in tungsten.
Most of the observed gamma-rays at the front surface of the assembly, 0 mm,
are produced by high energy neutron of > 1 MeV. At 76 mm, both halves of
observed gamma-rays are produced by neutrons of > 1 MeV and 0.01-1 MeV.
At 228 and 380 mm, neutrons with energy between 1 keV - 1 MeV contribute
predominantly to produce secondary gamma-rays.
Example of Experiment Analysis:
The sample input for the MCNP-4A code is given in file mcnp-w.inp. The
input was taken from [1], except that the 0 degree source was used instead
of the source subroutine (not provided in the document [1]).
Transport calculations with the MCNP-4A code are presented in [2]. The
calculations were performed using the JENDL-3.2, JENDL-FF and FENDL/E-1.0
nuclear data libraries.
The calculations were performed at the OECD/NEA Data Bank [5] using the
included MCNP inputs and the FENDL-2 (=JENDL-FF) and ENDF/B-VI.8 cross section
evaluations. The neutron spectra and the corresponding C/E ratios are
presented in Figures 3, 4 and 5. The measured fusion peak is wider than the
one calculated with the provided MCNP input. The gamma spectra obtained using
the ENDF/B-VI.3 data are shown in Figures 6, 7 and 8. They indicate reasonable
agreement between the experiment and the calculation.
6. Special Features:
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None
7. Author/Organizer:
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Experiment and analysis:
F. Maekawa, C. Konno, Y. Kasugai, Y. Oyama, Y. Ikeda
Japan Atomic Energy Research Institute
Tokai-mura, Naka-gun, Ibaraki-ken, 319-1195 Japan
Phone: 81-292-82-6809 (for Y.O.) or -6015 (for H.M.)
Fax: 81-292-82-5996 (for Y.O.) or -6365 (for H.M.)
E-mail: oyama@cens.tokai.jaeri.go.jp
or fujio@cens.tokai.jaeri.go.jp
Compiler of data for Sinbad:
S. Kitsos
OECD/NEA, 12 bd des Iles, 92130 Issy les Moulineaux, France
E-mail: stavros.kitsos@free.fr
Reviewer of compiled data:
I. Kodeli
OECD/NEA, 12 bd des Iles, 92130 Issy les Moulineaux, France
e-mail: ivo.kodeli@oecd.org
8. Availability:
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Unrestricted
9. References:
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[1] F. Maekawa, C. Konno, Y. Kasugai, Y. Oyama, Y. Ikeda:
“Data Collection of Fusion Neutronics Benchmark Experiment Conducted at
FNS/JAERI”, JAERI-Data/Code 98-021 (1998).
[2] F. Maekawa, M. Wada, C. Ichihara, Y. Makita, A.Takahashi, Y. Oyama:
“Compilation of Benchmark Results for Fusion Related Nuclear Data ”,
JAERI-Data/Code 98-024 (1998).
[3] F. Maekawa, C. Konno, K. Kosako, Y. Oyama, Y. Ikeda and H. Maekawa:
“Bulk Shielding Experiments on Large SS316 Assemblies Bombarded by
D-T Neutrons, Volume II: Analysis“, JAERI-Research 94-044 (1994).
[4] Y. Oyama: “Experimental Study of Angular Neutron Flux Spectra on a Slab
Surface to Assess Nuclear Data and Calculational Methods for a Fusion
Reactor Design“, JAERI-M 88-101 (1988).
[5] I. Kodeli, Recent Progress in the SINBAD Project, EFFDOC-866, EFF
Meeting, Issy-les-Moulinaux (April 2003)
References to other useful documents can be found in the above reports.
10. Data and Format:
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DETAILED FILE DESCRIPTIONS
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Filename Size[bytes] Content
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1 fnsw-abs.htm 20,069 This information file
2 fnsw-exp.htm 30,854 Description of experiment
3 mcnp-w.inp 12,010 Input data for MCNP-4A calculations
4 fnsw-1.gif 39,827 Fig. 1: Experimental assembly of tungsten
5 fnsw-2.gif 11,332 Fig. 2: Source neutron spectrum emitted towards the
0 degree from the target.
6 fnsw-3.gif 27,839 Fig. 3: Neutron spectra at z=76 mm in W (ref. [5])
7 fnsw-4.gif 29,378 Fig. 4: Neutron spectra at z=228 mm in W (ref. [5])
8 fnsw-5.gif 28,549 Fig. 5: Neutron spectra at z=380 mm in W (ref. [5])
9 fnsw-6.jpg 37,080 Fig. 6: Gamma-ray spectra at z=76 mm in W (ref. [5])
10 fnsw-7.jpg 36,395 Fig. 7: Gamma-ray spectra at z=228 mm in W (ref. [5])
11 fnsw-8.jpg 36,642 Fig. 8: Gamma-ray spectra at z=380 mm in W (ref. [5])
12 j98-021.pdf 6,886,161 Reference JAERI-Data/Code 98-021
13 j98-024.pdf 10,339,840 Reference JAERI-Data/Code 98-024
File fnsw-exp.htm contains the following tables:
Table 1: Material specification
Table 2: Systematic errors for neutron spectra measurements by NE213
Table 3: Dosimetry Reactions used in the foil activation method
Tables 4-5: Measured neutron spectra
Tables 6: Measured dosimetry reaction rates
Table 7: Gamma-ray spectra
Table 8: TLD Measurements
Figures are included in GIF and JPG formats.
SINBAD Benchmark Generation Date: 05/2003
SINBAD Benchmark Last Update: 05/2003