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Thermal and epithermal neutron fluence rates in the irradiation facilities of the TRIGA IPR-R1 nuclear reactor

Abstract

The TRIGA IPR-R1 nuclear reactor at the Centro de Desenvolvimento da Tecnologia Nuclear CDTN/CNEN, Belo Horizonte, Brazil, has three irradiation facilities: a rotary specimen rack outside the reactor core with 40 irradiation channels which provide large scale isotope irradiation; the central tube placed at the center of the reactor core which permits sample irradiation with maximum neutron flux, as well as neutron beam extraction; a pneumatic transfer tube which makes possible the analysis of short half-life radioisotopes. The aim of this work is to evaluate the thermal and epithermal neutron fluence rates in the three irradiation facilities of the IPR-R1. Al-0.1%Au reference materials were irradiated bare and Cd-covered, at 100 kW thermal power, and gamma spectrometry was applied with an HPGe detector. For the rotary specimen rack, the values obtained for thermal and epithermal neutron fluence rates are (8.2 ± 0.2) × 10(11)n.cm-2.s-1 and (3.5 ± 0.1) × 10(10)n.cm-2.s-1, respectively. For the pneumatic transfer tube and the central tube, epithermal neutron fluence rate values are respectively (3.3 ± 0.2) ×10(9)n.cm-2.s-1 and (2.6 ± 0.1) x 10(11)n.cm-2.s-1. For these facilities, thermal neutron fluence rate values are (2.5 ± 0.2) × 10(11)n.cm-2.s-1 and (2.8 ± 0.1) × 10(12)n.cm-2.s-1, respectively. Knowledge of these parameters will be fundamental in the planning of sample irradiation for analysis or radioisotope production in a more accurate way.

TRIGA IPR-R1 nuclear reactor; neutron fluence rate; neutron activation analysis; irradiation facilities


Thermal and epithermal neutron fluence rates in the irradiation facilities of the TRIGA IPR-R1 nuclear reactor

Dante Marco ZangirolamiI; Arno Heeren de OliveiraII; Andréa Vidal FerreiraIII

ICentro de Desenvolvimento da Tecnologia Nuclear CDTN/CNEN, Av. Presidente Antônio Carlos, 6627 – Campus UFMG, 31270-901, Belo Horizonte, MG, Brazil and Departamento de Engenharia Nuclear DEN/UFMG, Av. Antônio Carlos, 6627 – Campus UFMG, 31270-090 Belo Horizonte, MG, Brazil

IIDepartamento de Engenharia Nuclear DEN/UFMG, Av. Antônio Carlos, 6627 – Campus UFMG, 31270-090 Belo Horizonte, MG, Brazil

IIICentro de Desenvolvimento da Tecnologia Nuclear CDTN/CNEN, Av. Presidente Antnio Carlos, 6627 – Campus UFMG, 31270-901, Belo Horizonte, MG, Brazil

ABSTRACT

The TRIGA IPR-R1 nuclear reactor at the Centro de Desenvolvimento da Tecnologia Nuclear CDTN/CNEN, Belo Horizonte, Brazil, has three irradiation facilities: a rotary specimen rack outside the reactor core with 40 irradiation channels which provide large scale isotope irradiation; the central tube placed at the center of the reactor core which permits sample irradiation with maximum neutron flux, as well as neutron beam extraction; a pneumatic transfer tube which makes possible the analysis of short half-life radioisotopes. The aim of this work is to evaluate the thermal and epithermal neutron fluence rates in the three irradiation facilities of the IPR-R1. Al-0.1%Au reference materials were irradiated bare and Cd-covered, at 100 kW thermal power, and gamma spectrometry was applied with an HPGe detector. For the rotary specimen rack, the values obtained for thermal and epithermal neutron fluence rates are (8.2 ± 0.2) × 1011n.cm-2.s-1 and (3.5 ± 0.1) × 1010n.cm-2.s-1, respectively. For the pneumatic transfer tube and the central tube, epithermal neutron fluence rate values are respectively (3.3 ± 0.2) ×109n.cm-2.s-1 and (2.6 ± 0.1) x 1011n.cm-2.s-1. For these facilities, thermal neutron fluence rate values are (2.5 ± 0.2) × 1011n.cm-2.s-1 and (2.8 ± 0.1) × 1012n.cm-2.s-1, respectively. Knowledge of these parameters will be fundamental in the planning of sample irradiation for analysis or radioisotope production in a more accurate way.

Keywords: TRIGA IPR-R1 nuclear reactor, neutron fluence rate, neutron activation analysis, irradiation facilities

1. INTRODUCTION

The IPR-R1 is a TRIGA Mark 1 reactor produced by General Atomics (USA). This reactor belongs to the Centro de Desenvolvimento da Tecnologia Nuclear CDTN/CNEN, located in the City of Belo Horizonte, Brazil, and has been operating since 1960 [1]. It is a pool type reactor cooled by natural circulation. The current (2009) core configuration has 63 fuel elements which consist of an alloy of zirconium hydride and uranium enriched to 20% uranium-235. Reactor power level is controlled by three control rods containing boron carbide. The principal instrumentation for the operation of the IPR-R1 TRIGA Mark 1 consists of four neutronic channels for measuring power, as well as channels for monitoring temperature, water conductivity, radiation level, etc. Figure 1 shows a diagram of the IPR-R1 pool and reactor core.


Figure 2 shows a horizontal cross-section of the actual reactor core configuration where it is possible to see the three irradiation facilities: the rotary specimen rack (RSR) outside the reactor core with 40 irradiation channels which provide large scale isotope irradiation; the central tube (CT) placed at the center of the reactor core which permits sample irradiation with maximum neutron flux, besides neutron beam extraction; the pneumatic transfer tube (PTT) which makes possible the analysis of short half-life radioisotopes. One of the main applications of the IPR-R1 is neutron activation analysis, NAA. Approximately 3000 samples are analyzed annually by this technique and, in most cases, samples are irradiated in the RSR.


The IPR-R1 core configuration has been changed six times. The original core configuration allowed steady-state operation at 30 kW [1]. The current core configuration, from 2001, permits operations at a maximum steady-state power of 250 kW [2]. Our previous work [3] on the present core configuration evaluated the specific induced activity profile at the RSR and its variation under different irradiation conditions. For the actual core configuration, there are few experimental works concerning the characterization of the thermal and epithermal neutron fluence rates in IPR-R1 irradiation facilities. An experimental work [4] has evaluated the thermal and epithermal neutron fluence rates in five channels of the RSR. Thermal and epithermal neutron fluence rates in the PTT facility and epithermal neutron fluence rate in the CT facility have not been evaluated until now. Therefore, it is very important to evaluate and to update the data concerning the neutron fluence rates in IPR-R1 irradiation facilities. Knowledge of these parameters is fundamental to the planning of sample irradiation for analysis or radioisotope production. It permits calculation of neutron reaction rates in experiments, enabling determination of experimental parameters such as specific induced activity, irradiation time, counting time, decay time, etc. The aim of the present work is to determine the thermal and epithermal neutron fluence rates in eight specific channels of the RSR, in the central position of the CT and in the PTT irradiation facilities of the TRIGA IPR-R1 nuclear reactor.

2. MATERIALS AND METHODS

The thermal and epithermal neutron rates in the IPR-R1 irradiation facilities were measured by the neutron activation method using bare and cadmium-covered foils [5]. Irradiations were performed between May and October, 2008. Al-0.1%Au reference material [6] was used as the neutron fluence rate detector. The reference material was cut into disks about 1cm in diameter and weighed on a precision balance. Each detector was approximately 23mg. The experimental procedure for each of the irradiation facilities are described below. All the experiments were performed at 100kW thermal power.

Rotary Specimen Rack:

Eight irradiation channels were chosen for the measurements: channels 5, 10, 15, 20, 25, 30, 35, 40. Previous work [3] had revealed that the specific induced activity of samples in the RSR has a fluctuation of approximately 2% for samples irradiated on different dates. In order to check variations of thermal and epithermal neutron fluence rates, bare and Cadmium-covered probes were irradiated in the selected irradiation channels on different dates. On any given date, reactor operational parameters, such as pool water temperature, control rod positions, etc., may present slight differences which reflect on induced activity in samples. In this experiment set, probes were irradiated for 1 hour. Another experiment was performed to determine thermal and epithermal neutron fluence rates in a single irradiation, in order to ensure the same reactor operating conditions. After reactor startup and power stabilization, sixteen probes were irradiated, one at a time, in the selected channels. Each probe was irradiated for 5 minutes. For each irradiation channel, two probes were used, one bare and one cadmium-covered. The reactor operation parameters remained stable during the experiment, which lasted approximately 3 hours.

Central Tube and Pneumatic Transfer Tube

For measuring CT and PTT neutron fluence rates, irradiations were performed on different dates. Bare and Cadmium-covered probes were irradiated one at a time. In these experiments, probes were irradiated for 1 hour. For CT and PTT analysis, six and seven irradiations were performed respectively.

After neutron irradiation and appropriate decay time, probes were submitted to gamma spectrometry in a system equipped with an HPGe detector CANBERRA® 5019 and Gennie 2000 v2.0, CANBERRA® software. The counting time was adjusted to provide a net peak area of at least 20,000 countings for the 411.8keV peak from the 198Au radioisotope. Gamma spectrometer analyses provide the induced activity of the probes at each irradiation.

The characteristic nuclear reactions in the experiments are:

198Au radioisotope has a half-life of 2.694 days, while the 28Al radioisotope has a half-life of 2.24 minutes. Therefore, half an hour after ending irradiation, almost all 28Al will have decayed without disturbing the 198Au counting.

Adopting the Högdahl convention [7], the sample induced activity A0 at the end of the irradiation time tirr, is given by:

where N is the number of target nuclei in the sample; σth is the thermal neutron radioactive capture cross-section of the target nuclei; thand epi are the thermal and epithermal neutron fluence rates, respectively, in the samples; Iγ is the radioactive capture resonance integral of the target nuclei; λ is the radioisotope decay constant (λ= ln2/T1/2; T1/2 is the radioisotope half-life). After gamma spectrometry analysis, the induced activity may be obtained by [7]:

where td is the time interval between the termination of irradiation and the start of counting; tm is the counting interval time; e is the photo peak counting efficiency; θ is the isotopic abundance of the target nuclide; γ is the gamma emission probability; w is the target nuclide mass in the sample; Np is the net peak area.

When samples are irradiated under Cadmium cover, the (

th σth) term is much smaller than the (epi Iγ ) term, because Cadmium cover almost completely absorbs the thermal neutrons and transmits all the epithermal neutrons. Therefore equation (3) becomes:

From equations (4) and (5), the neutron epithermal fluence rate

epi may be determined directly.

The ƒ parameter, defined as the thermal to epithermal neutron fluence rate ratio, is given by [6]:

where

0 is the ratio of the radioactive capture resonance integral and the thermal neutron radioactive capture cross-section of the target nuclei; RCd is the Cadmium ratio, defined as the ratio of the activity of the bare sample to the activity of the Cadmium covered sample; FCd is the correction factor for Cadmium transmission of epithermal neutrons. When a bare and a Cadmium-covered sample are irradiated by a stable neutron flux in an irradiation channel, 0, FCd and RCd are constants, experimentally determined, which permits determination of ƒ. Therefore, if the ƒ parameter is known, the thermal neutron fluence rate is obtained by:

3. RESULTS AND DISCUSSIONS

Rotary Specimen Rack:

Figure 3 shows the results of specific induced activity on bare and cadmium-covered probes at different irradiations.


The results indicate a variation of 2.7% for values for induced activity on bare probes and a variation of 4.9% for values for induced activity on cadmium-covered probes. Results for bare samples are consistent with previous work [4], while the results for cadmium-covered probes were measured for the first time in this work. These results permit one to state that thermal and epithermal neutron fluence rates in the IPR-R1 RSR have a fluctuation less than or equal to 5% in different reactor operations.

The obtained values for thermal and epithermal neutron fluence rates in the chosen RSR irradiation channels are shown in Figure 4.


The mean values and standard deviations for thermal and epithermal neutron fluence rates at the RSR are respectively

th=(8.2x1011 ± 2%)n.cm-2.s-1 and epi=(3.5x1010 ± 3%)n.cm-2.s-1, which correspond to ƒ=24. The values obtained in this work are respectively 30% and 20% higher than the previous results reported by other authors [4]. This difference may be due to the time lapse between the two works. The IPR-R1 reactor is periodically submitted to thermal calibration, the last one being carried out on March 5th, 2009 [8]. At that time, the value of the thermal power obtained by the heat balance method was (112.0 ± 6.6) kW. This value indicates that the difference between 100kW nominal thermal power and the experimental power value may roughly reach 20%, which explains our higher results when compared to those previous [4].

Central Tube:

The values obtained for thermal and epithermal fluence rates in the CT central position are:

th = (28.0 x1011± 4%) n.cm-2.s-1 and epi = (26.0 x1010± 4%) n.cm-2.s-1. These values are 3.4 and 7.4 times higher than those obtained for the RSR facility. The ratio of thermal to epithermal neutron fluence rates in the CT is ƒ = 11. This value is two times smaller than those observed for the RSR and indicates that neutron moderation increases with the distance from the core central position, as expected.

Pneumatic Transfer Tube:

The values obtained for thermal and epithermal fluence rates in the PTT are: th =(2.5 × 1011 ± 8%) n.cm-2.s -1 and epi =(3.3x109 ± 6%) n.cm-2.s-1. The ratio of thermal to epithermal neutron fluence rate in the PTT is ƒ =75, which is almost 5 times greater than the value obtained for the central tube.

Table 1 summarizes the results for neutron fluence rates in the IPR-R1 irradiation facilities.

4. CONCLUSIONS

In this work, thermal and epithermal neutron fluence rates were determined for the three irradiation facilities of the IPR-R1 reactor at the CDTN/CNEN.

The mean values and standard deviations for the thermal and epithermal neutron fluence rates in the RSR are respectively

th = (8.2 × 1011 ± 2%)n.cm-2.s-1 and epi = (3.5 × 1010 ± 3%)n.cm-2.s-1, which correspond to ƒ =24. The values obtained for the thermal and epithermal fluence rates in the CT central position are: th = (28.0 × 1011 ± 4%) n.cm-2.s-1 and epi = (2.6 × 1011 ± 4%) n.cm-2.s-1. The ratio of thermal to epithermal neutron fluence rate in the CT is ƒ =11. The values obtained for thermal and epithermal fluence rates in the PTT are: th = (2.5 × 1011 ± 8%) n.cm-2.s-1 and epi = (3.3 × 109 ± 6%) n.cm-2.s-1. The ratio of thermal to epithermal neutron fluence rates in the PTT is ƒ =75.

The results reveal that the epithermal neutron fluence rate in the PTT facility is approximately ten times smaller than that in the RSR which is about seven times smaller than that in the CT. In the case of the thermal neutron fluence rate, the rate ratio between the CT and the RSR or the RSR and the PTT is about three. These results show clearly the neutron thermalization from the center to the periphery of the reactor core, as expected. The ƒ parameter at the RSR is about two times higher than that for the CT, while for the PTT the ƒ value is about seven times higher than the CT value.

Knowledge of the thermal and epithermal neutron fluence rate in the irradiation facilities of the TRIGA IPR-R1is fundamental in the planning of sample irradiation for analysis or radioisotope production in a more accurate way. It will permit the calculation of the actual neutron reaction rates in the different irradiation channels, which will enable the determination of parameters such as specific induced activity, irradiation time, counting time, decay time, etc., for different experimental works. In a future article, the experimental values obtained in this work will be compared with results from a Monte Carlo simulation of IPR-R1 neutronic parameters.

5. ACKNOWLEDGEMENTS

The authors would like to thank Dr. Amir Z. Mesquita, Fausto M. Júnior, M.Sc, supervisors of the TRIGA IPR-R1 reactor, as well as reactor operators Paulo F. Oliveira and Luiz O.I.S. Câmara. We are grateful to Geraldo F. Kastner, M.Sc, Dr. Rose M. G. P. Souza and Dr. Maria Â.B.C. Menezes for invaluable technical discussions.

(Received on 25 September, 2009)

  • [1] J.M. Lima, V.M. Andrade, Transactions of the American Nuclear Society 11, 270 (1968).
  • [2] H.M. Dalle, C. Pereira, R.G.P. Souza, Annals of Nuclear Energy 29, 901 (2002).
  • [3] D.M. Zangirolami, A.V. Ferreira, A.H. Oliveira, Brazilian Journal of Physics 39, 260 (2009).
  • [4] M.Å .B.C. Menezes, R. Jacimovic, Nuclear Instruments & Methods in Physics Research A 564, 707 (2006).
  • [5] K.H. Beckurts, "Neutron Physics", Springer-Verlag, New York, USA, (1964).
  • [6] Institute for Reference Materials and Measurements, Certified reference material IRMM-530R, Certificate of analysis, Gold mass fraction in Al-0.1 % Au Alloy. Geel, Belgium, (2007).
  • [7] F. de Corte, The k0-Standardization Method. A Move to the optimization of Neutron Activation Analysis, Thesis, Gent University, Belgium (1987).
  • [8] A.Z. Mesquita, H.C. Rezende, R. M. G. P. Souza, Proceedings of the 20th International Congress of Mechanical Engineering, Gramado, RS, Brazil, (2009).

Publication Dates

  • Publication in this collection
    22 Apr 2010
  • Date of issue
    Mar 2010

History

  • Received
    25 Sept 2009
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