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Impact of photoneutrons on reactivity measurements for TMSR-SF1

NUCLEAR ENERGY SCIENCE AND ENGINEERING

Impact of photoneutrons on reactivity measurements for TMSR-SF1

Rui-Min Ji
Ming-Hai Li
Yang Zou
Gui-Min Liu
Nuclear Science and TechniquesVol.28, No.6Article number 76Published in print 01 Jun 2017Available online 28 Apr 2017
55303

The solid-fueled thorium molten salt reactor (TMSR-SF1) is a 10 MWth test reactor design to be deployed in 5 to 10 years by the TMSR group. Its design combines coated particle fuel and molten FLiBe coolant for great intrinsic safety features and economic advantages. Due to a large amount of beryllium in the coolant salt, photoneutrons are produced by (γ, n) reaction, hence the increasing fraction of effective delayed neutrons in the core by the photoneutrons originating from the long-lived fission products. Some of the delayed photoneutron groups are of long lifetime, so a direct effect is resulted in the transient process and reactivity measurement. To study the impact of photoneutrons for TMSR-SF1, the effective photoneutron fraction is estimated using k-ratio method and performed by the Monte Carlo code (MCNP5) with ENDF/B-VII cross sections. Based on the coupled neutron-photon point kinetics equations, influence of the photoneutrons is analyzed. The results show that the impact of photoneutrons is not negligible in reactivity measurement. Without considering photoneutrons in on-line reactivity measurement based on inverse point kinetics can result in overestimation of the positive reactivity and underestimation of the negative reactivity. The photoneutrons also lead to more waiting time for the doubling time measurement. Since the photoneutron precursors take extremely long time to achieve equilibrium, a "steady" power operation may not directly imply a "real" criticality.

TMSR-SF1Delayed photoneutronsCoupled neutron-photon point kineticsReactivity measurement.

1 Introduction

In recent years, fluoride-cooled high-temperature reactors (FHRs) have gained much attention worldwide due to the potential of achieving outstanding economic performance while meeting high standards for reactor safety and security [1-3]. With superior nuclear properties and heat-transfer characteristics, the FLiBe salt (LiF-BeF2) becomes the most convincing medium for FHRs with thermal neutron spectrum [4]. The Thorium Molten Salt Reactor (TMSR) group in China proposed its research program [5-6] including a 10 MWth solid-fueled thorium molten salt reactor (TMSR-SF1). In this design, about 15,000 pebbles are loaded in the core cavity and about 5 m3 FLiBe salt are filled in the primary loop.

Because of the large amount of beryllium in the core, photoneutrons are generated in the active region via (γ, n) reaction. In general, photoneutrons have little contributions to the overall neutron balance. They affect reactor power level in a negligible manner. However, there are some photoneutrons that are indirectly generated from fission, hence the term of delayed neutrons. Since photoneutrons have insignificant contribution to the fraction of effective delayed neutron and the equilibrium state is difficult to reach, the photoneutrons are often neglected, which results in measurement errors [7-12]. In VVRSZM type research reactor of KFKI-AEKI [10], which uses beryllium reflector, the reactivity meter gave false values because the photoneutrons were not taken into account. In HW-1, a uranium-fueled and heavy water moderated reactor built in China, it is observed that the critical water level is different at different power levels. In the rod-drop measurement on the LITR reactor of beryllium reflector, an underestimation of 6 % was seen in the results by neglecting the photoneutrons [12].

In this paper, the impact of photoneutrons on reactivity measurement for TMSR-SF1 is investigated using neutron-photon coupled point kinetic equations. The methods are introduced in Section 2. The results are presented in Section 3. The conclusions are given in Section 4.

2 Methods

2.1. The k-ratio method

In 1997, Bretscher of the Argonne National Laboratory introduced the k-ratio method to evaluate the delayed neutron fraction [13]. According to this method, the fraction of effective delayed neutron can be evaluated by the ratio between the prompt and the total multiplication factors, hence the name of k-ratio method,

βeff=χdυdχυ=1χυχdυdχυ=1χυp(χdχ)υdχυ1χpυpχυ=1kpk (1)

where υ, υd and υp are average numbers of the total fission neutrons, delayed fission neutrons and prompt fission neutrons, respectively, produced per fission; χ, χd and χp are spectra of the three neutron categories, respectively. The approximation in Eq. (1) is based on two assumptions: 1) (χdχ)υd is at least two orders of magnitude smaller than the χυp, because υd is two orders of magnitude smaller than υp; and 2) χp is almost equal to χ.

The k-ratio method can be performed by Monte Carlo code (MCNP) which can suppress the delayed neutrons in the critical calculation. In this paper, MCNP5 (ver1.51) and ENDF/B-VII are used. The fraction of effective delayed fission neutrons (βn), which are decayed by the fission products, is modeled by MCNP calculation (MODE N) with and without the delayed neutron (TOTNU card) while ignoring photoneutrons. βn can be estimated by Eq. (2)

βn=ktnkpnktn (2)

where the superscript n stands for MODE N, the subscript t and p denote the neutron transportation with and without the delayed neutron, respectively. As an extension, the contribution of photoneutrons (βph) can be obtained by coupled neutron-photon transport (MODE N P) with MPN card to model (γ, n) reaction [8],

βph=βtotalβn=ktn+pkpnktn+pktnkpnktn (3)

where the superscript n+p stands for MODE N P.

There is an approximation in the simulation. Because MCNP does not simulate the delayed particles in critical calculations, the prompt gammas emitted in the process of fission and neutron capture are used, instead of delayed gammas which are emitted in the decay process of the fission products and activation products. It is reasonable, as the difference is small between the prompt and delayed photon spectra from 235U fission represented by empirical Eqs. (4) and (5) [8, 14].

χpγ(E)νpγ[photonsfission1MeV1]=8.0exp(1.1E), (4) χdγ(E)νdγ[photonsfission1MeV1]=7.4exp(1.1E). (5)
2.2. The neutron-photon coupled point kinetics equations

With the infinite-velocity approximation, we can get the conventional set of point kinetics equations as Eqs.(6–8). The physical interpretation of this approximation is that the photons are transported instantaneously following a change. This approach has been used for fast neutrons in the neutron-only multi-group transportation [14]. Since the speed of photons is at least one order of magnitude greater than the neutron speed, it is more reasonable here.

dn(t)dt=ρβeffΛnn(t)+iλiCi+jλjCj, (6) dCi(t)dt=βinΛnn(t)λii (7) dCj(t)dt=βjphΛnn(t)λjCj (8)

where n(t) is neutron flux (or power), Ci is concentration of the ith group of neutron precursors, λi is decay constant of the ith neutron precursors, Cj=ρphΛγ/(ΛnPj) is concentration of the jth group artificially introduced photoneutron precursors, ρph is the photoneutrons reactivity (photoneutron production rate over photo removal rate), Pj is concentration of the jth group photoneutron precursors, λj is decay constant of the jth photoneutron precursor. Λn is neutron generation time, ρ*≡ ρ + ρph is the total reactivity, βeff = i βin + j βjph is the total effective delayed neutron fraction, βin is the ith group delayed fission neutron fraction, βjph is effective fraction of the jth group delayed photoneutrons, and Λγ is photon generation time.

The coefficients of βeff and Λn are assumed to be independent of time. This is already the case for the exact point kinetic without photoneutron terms. The photoneutron reactivity is contributed by the gamma ray (both prompt and delayed) reactivity. Also, it is no need to calculate the photon generation time (Λγ) and the photoneutron precursor’s concentration (Pj) to get the artificial photoneutron precursor group Cj for the dynamic behavior of the reactor [14].

As listed Table 1, the traditional 6 group delayed fission neutrons parameters per 235U fission [15], and the additional 9 group delayed photoneutrons parameters per 235U fission in infinite beryllium, are used together with the corrected effective fraction of the photoneutrons.

Table 1.
Traditional delayed fission neutron parameters and additional photoneutron parameters [15]
Delayed neutrons Delayed photoneutrons
i λi (s−1) βi (×10−4) j λj (s−1) βj (×10−5)
1 0.0124 2.47 1 6.24×10−7 0.057
2 0.0305 13.85 2 2.48×10−6 0.038
3 0.111 12.22 3 1.59×10−5 0.260
4 0.311 26.45 4 6.20×10−5 3.2
5 1.14 8.32 5 2.67×10−4 0.36
6 3.01 1.69 6 7.42×10−4 3.68
      7 3.60×10 1.85
      8 8.85×10−3 3.66
      9 2.26×10−2 2.07
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2.3. Interpretation of reactivity measurements

Because of the photoneutrons in the core, the in-hour equation used to convert a measured stable doubling period T into a reactivity ρ should be modified as Eq. (9) [10].

ρ($)βeff=0.693ΛnT+iβin1+Tλi0.693+jβjph1+Tλj0.693. (9)

Similarly, for the interpretation of inverse kinetics measurements, the time dependent reactivity ρ(t) obtained by the evolution of the neutron population are modified as Eq.(10) [16, 17].

ρ(t)βeff=1+Λnβeffn(t)dn(t)dtΛnβeffn(t)i=16λiCi0BFieλit1βeffn(t)0tn(t')i=16λiβieλi(tt')dt'Λnβeffn(t)j=19λjCj0BFjeλjt1βeffn(t)0tn(t')j=19λjβjeλj(tt')dt', (10)

where, Cj0 and Ci0 are the equilibrium concentration of neutron and photoneutron precursors, respectively; BFi and BFj are the build-up factors which account for the building up of delayed neutron and photoneutron precursors, respectively, prior to the actual measurement. The building factors can be derived from the power history before the measurement via Eq.(11), where, n0 is the neutron flux at full power and Tb is the building up time.

BFi=λiTb0n(t)n0eλit'dt'. (11)

3 Results

MCNP5 is used for explicitly representing the geometry of TMSR-SF1, as shown schematically in Fig. 1. The graphite reflectors build up the core cavity and host the control rods and instruments. Fuel pebbles of Φ6 cm are filled in the core cavity and cooled by the FLiBe salt. Details of TMSR-SF1 can be found in Refs. [6, 19].

Fig. 1
The MCNP model for TMSR-SF1.
pic
3.1. The delayed fission neutron and photoneutron fraction

Using the k-ratio method described in Section 2.1, the delayed fission neutron and photoneutron fraction of TMSR-SF1 were simulated with 109 neutrons, as the (γ, n) reaction rate is very small. The critical eigenvalues were obtained with a statistical uncertainty of about 0.00003. The results are given in Table 2. The effectiveness fraction of the delayed fission neutron is about 1.04 in Mode N, while it is 0.27 for the 235U fission [15]. The k-ratio method is very time consuming for low statistical errors. Besides, photoneutrons generated in the active core and the reflector zones are of the same importance in the k-ratio method. Considering TMSR-SF1 has much more coolant in the reflector zone than in the active zone, the k-ratio method may overestimate the delayed photoneutron fraction.

Table 2.
Calculation of the effectiveness fractions for TMSR-SF1 by the k-ratio method
  βn (pcm) βph (pcm)
TMSR-SF1 679 ± 1.4 4 ± 1.4
235U fission 650 15
Effectiveness fraction 1.04 0.27
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3.2. Influence of photoneutrons on real time reactivity

The real time reactivity measurement, i.e. the reactivity meter, has been used widely [16, 17]. In this section, both positive and negative reactivity insertions are simulated. The theoretical basis is inverse point kinetics descried in Section 2.3.

3.2.1. Negative reactivity insertion

The largest impact of the photoneutrons is expected after shut-down of the reactor that has been operated at high power for a long time. According to the design of TMSR-SF1, the total worth of safety rods is about 6 $ [6], and they should be fully inserted in 6 s at emergency. Such a scram was calculated. In the first 10 s, the reactor is operated at full power, then 6 $ negative reactivity is fully inserted in 6 s.

The relative power level as a function of time following a scram from the full power is shown in Fig. 2(a). In the calculation represented by “6 Group”, the photoneutrons were not taken into account. Meanwhile, the one denoted by “15 Group”, the photoneutrons were included in the calculation. The power difference between two cases grew gradually after shut-down. In the first 100 s, they did not differ from each other because the fission neutrons still took the major part. About 500 s latter, the presence of photoneutrons led to a 10 times larger power level. This can be explained by Eqs. (6–8). After shut-down, the number of photoneutrons was still determined by the original power, while the number of the fission neurons depended on the current low power. The relatively long decay time of relevant fission products made photoneutrons play an important role after shut-down.

Fig. 2
Calculation of negative reactivity insertion (15 Group: with photoneutrons; 6 Group: without photoneutrons.)
pic

The time dependent reactivity calculated with and without considering photoneutrons is shown in Fig. 2(b). In this simulation, the relative power obtained with photoneutrons is regarded as the truth (the blue line in Fig. 2a). One sees that, with photoneutrons, the reactivity meter gives great values; whereas it gives false values without photoneutrons. Although the reactor keeps subcritical after the scram, the reactivity meter without photoneutrons shows that positive reactivity is inserted gradually.

3.2.2. Positive reactivity insertion

To evaluate the influence on positive reactivity, 0.1 $ was inserted after full power operation for a long time. The power evolution after the positive reactivity insertion, shown in Fig. 3(a), was simulated with and without the photoneutrons. It can be seen that the effect of delayed photoneutrons is similar to the delayed fission neutrons. The presence of photoneutrons slowed down the power increase. After 200 s of the reactivity insertion, “6 Group” power led to a power level of 10 times larger than the origin power; while the “15 Group” power led to a power level of 9 times larger than the origin level. The power evaluated with photoneutrons (blue line in Fig. 3a) was considered as the real case. The time dependent reactivities calculated with and without the photoneutrons are shown in Fig. 3(b). With photoneutrons, the reactivity meter met the truth; whereas the reactivity was overestimated when photoneutrons were neglected.

Fig. 3
Calculation of positive reactivity insertion (15 Group: with the photoneutrons; 6 Group: without the photoneutrons.)
pic
3.3. Influence of photoneutrons on doubling time measurement

The doubling time method is widely used for the control rod worth measurement, where the reactivity is calculated by the in-hour equation using the doubling time. The doubling time as a function of the positive reactivity inserted is shown in Fig. 4. In this calculation, follow the regulations, the doubling time was 30 s to 180 s. As expected, the doubling time became longer for the same reactivity insertion by considering the photoneutron contribution. The 60 s doubling time corresponds to 0.108 $ reactivity insertion for “6 Group”; whereas to 0.112 $ for “15 Group”.

Fig. 4
Relationship between the doubling time and the positive reactivity inserted
pic

In order to choose an appropriate waiting time before the reactivity measurement with respect to the positive reactivity insertion, calculations were carried out at different reactivities. The waiting time needed for 2% deviation from the doubling period is shown in Fig. 5(a). The discrepancy in the waiting time was almost negligible for doubling periods close to 30 s, but became more apparent for longer doubling time. At 180 s of doubling time, the waiting time was less than 100 s for “6 Group”, but over 250 s for “15 Group”.

Fig. 5
Calculation of period deviation at 100 s and 108 s of building time, as a function of waiting time.
pic

Since long lived photoneutron precursors take extremely long time for saturation, it is not appropriate to always set the precursors’ concentrations as equilibrium condition. In this context, the building time is used to define the holding time at full power level before the shut-down step. The building time effect on the period measurement was calculated with 0.1 $ reactivity insertion. The error in doubling period measurement as the function of waiting time is shown in Fig. 5(b). Obviously, much less waiting time is required in the non-equilibrium cases to reach the same accuracy as the equilibrium cases. When the reactor is at critical without external source, the equilibrium precursors to neutron flux is proportional to 1/λi. The equilibrium precursors play an important role for the reactor of a positive period. The ones with non-equilibrium precursors have shorter asymptotic period. It increases more rapidly than the equilibrium case, so less waiting time is needed for the doubling period measurement.

3.4. Influence of photoneutrons on criticality estimation

Criticality measurements play an important role in reactor experiments. It is a usual method to bring the reactor to a steady power representing criticality. However, the limitation is that the effective multiplication factor, keff, equals to one only when the delayed neutron precursors have reached equilibrium. Since the delayed photoneutrons have much longer half-life than the delayed fission neutrons, it takes fairly long time to reach the equilibrium or decay from the equilibrium. Two conditions, non-saturated photoneutron precursors and extra precursors compared to the equilibrium, were analyzed.

3.4.1. Non-saturation of the delayed photoneutron precursors

With increasing precursors, more neutrons are being consumed than yielded when the power is steady. Thus, there is a net deficit in the neutron balance and some excess keff is required to keep the power steady. For math simplicity, it was assumed that the reactor was brought up to given power instantaneously and all precursors’ concentrations were zero at the origin. Furthermore, the reactivity is constrained to maintain steady power, i.e., dn/dt = 0. A Matlab code was written to find the root of Eqs.(6–8).

The excess k required to keep the power steady after startup is shown in Fig. 6. In this calculation, different effectiveness factors were assumed. It can be predicted that, the fission neutron precursors got equilibrium in 15 minutes while the photoneutron precursors did not reach equilibrium in 2 hours. Hence, the reactor would need excess reactivity, about a few pcm, even after one or more hours. This may lead some trouble for high-precision measurements. As mentioned before, it was assumed that the reactor was brought up to steady power very rapidly, which is impossible in practice. So we made a correction for the finite start-up time by adding the time equal to the period that the reactor spent on bringing up the power. It should be emphasized that this effect applies only when the reactor is brought to power from shutdown. If the rector restores the steady power, the precursor equilibrium would be essentially undisturbed and no waiting time is needed for the criticality measurement.

Fig. 6
Excess k required to hold steady power after startup with and without the photoneutrons
pic
3.4.2. Extra photoneutron precursors compared to the equilibrium

After operating at the high power level for a long time, the delayed photoneutrons originated from the fission products would decay slowly after the shutdown. As long as the delayed photoneutrons are strong enough, the reactor can restart without the external source which has been demonstrated in PIK reactor and MNSRs, where heavy water and beryllium are uses as the reflector [7, 18]. Similar to the last section, there is a net gain in the neutron balance and negative keff is required to keep the power steady when there are extra photoneutron precursors compared to the equilibrium.

4 Conclusions

In this work we focused on addressing the impact of the photoneutrons in TMSR-SF1. The photoneutron contribution was calculated using k-ratio method by the MCNP5 code. Based on the coupled neutron-photon kinetics, the impact of the delayed photoneutrons was demonstrated in reactivity measurements. Conclusions drawn from this study are as follows:

1) The result shows that the delayed fission neutron fraction in TMSR-SF1 is about 680 pcm; whereas the delayed photoneutron fraction is only 4 pcm. Although significant computational time was consumed to reduce the statistical uncertainty, the delayed photoneutron fraction obtained is not accurate.

2) The presence of photoneutrons makes TMSR-SF1 more sluggish than the reactors without photoneutrons. The largest impact of photoneutrons can be found after the shut-down. The asymptotic period of the positive reactivity is greater than the case without photoneutrons. The critical extrapolation costs additional time due to the photoneutrons presence.

3) Omitting photoneutrons in on-line reactivity measurement can lead to overestimation of the positive reactivity and underestimation of the negative reactivity.

4) For the doubling time measurements, the presence of photoneutrons can increase the doubling time and the waiting time both. The increase in the waiting time is much more pronounced than that in the doubling time.

5) Since the photoneutron precursors take very long time to reach equilibrium, the “steady” power operation may not directly imply a “real” criticality. If the precursors are unsaturated, the TMSR-SF1 needs slightly excessive reactivity to operate at steady power.

Since the delayed photoneutrons impact the reactivity measurement greatly for TMSR-SF1, the effectiveness of the photoneutrons will be further studied in the near future. Another reason is that the result calculated by the k-ratio method is not sufficiently accurate due to large statistical uncertainties.

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