Keywords

8.1 Experimental Settings

8.1.1 Core Configuration

The experiments of reactivity measurement [1, 2] were carried out in the A cores (EE1 and E3 cores in Figs. 8.1a, b, respectively) that have polyethylene moderator and reflector rods, and different fuel assemblies: “F” and “f” (Figs. 8.2a, b, respectively). In EE1 core (Fig. 8.1a), fuel assembly “F” (1/8″P60EUEU) in Fig. 8.2a is composed of 60 unit cells, and upper and lower polyethylene blocks about 25″ and 20″ long, respectively, in an aluminum (Al) sheath (2.1″ × 2.1″ × 60″). For the fuel assembly, a unit cell in the fuel region is composed of two highly enriched uranium (HEU) fuel plates 1/8″ (2 × 1/16″) thick and a polyethylene moderator plate 1/8″ thick. In E3 core (Fig. 8.1b), another fuel assembly “f” (3/8″P36EU) in Fig. 8.2b is composed of 36 unit cells with an HEU fuel plate 1/16″ thick, polyethylene plates 3/8″ thick, and upper and lower polyethylene blocks about 23″ and 21″ long, respectively, in the Al sheath as in fuel assembly “F”. The neutron spectrum in EE1 core is compared with that in E3 core as shown in Fig. 8.3, demonstrating representatively hard (EE1 core) and soft (E3 core) neutron spectra in the KUCA A-core.

Fig. 8.1
figure 1

Top view of KUCA A-core (Refs. [1, 2])

Fig. 8.2
figure 2

Description of fuel rods in A-core shown in Fig. 8.1 (Refs. [1, 2])

Fig. 8.3
figure 3

Neutron spectra of EE1 and E3 cores shown in Figs. 8.1a, b, respectively (Refs. [1, 2])

8.1.2 Reactivity Measurements

For measuring the excess reactivity, the critical state was adjusted by maintaining a certain position of C3 rod in EE1 core and C1 rod in E3 core, and by withdrawing fully the other control (C1 and C2 in EE1; C2 and C3 in E3) and safety (S4, S5, and S6) rods from the core, respectively. Furthermore, excess reactivities in EE1 and E3 cores were measured by the positive period method, when C3 and C1 rods, respectively, were, under the critical state, fully withdrawn from the core.

For measuring the control rod worth, in cases of C1 and C2 rods in EE1 core, criticality was maintained by C3 rod, and the control rod worth of C1 or C2 rod was acquired by the rod drop method, after full insertion of C1 or C2 rod into the core. For C3 rod in EE1 core, criticality was adjusted by C1 rod, and the control rod worth of C3 rod was obtained by the rod drop method, after the full insertion of C3 rod into the core. Almost the same procedures were followed for the E3 core, with the use of the rod drop method, and the control rod worth of C1, C2, and C3 rods was obtained experimentally.

To estimate the experimental uncertainty of excess reactivity and control rod worth, the dimensions of the HEU plate comprising of core components are considered manufacturing tolerances among the significant factors taken into account, as shown in Table 8.1. In addition to the dimensions of the HEU plate, as previously demonstrated at the Fast Critical Assembly in the Japan Atomic Energy Agency [3], other important uncertainty factors include mechanical reproducibility of control rod position, measurement errors of doubling time by the positive period method, core temperature, delayed neutron parameters induced by numerical analyses, fuel composition uncertainty caused by heterogeneity distribution and deformation inside the Al sheath. Among these factors, the mechanical reproducibility of control rod position, in this study, was considered of great impact caused by tolerance and instability of control rod inside the Al sheath in a horizontal direction than the experimental uncertainty of excess reactivity and control rod worth, because the other uncertainties are relatively minor. Furthermore, heterogeneous arrangement of fuel plates in an axial direction was attributable to random selection of fuel plates for making fuel cells with a record number of fuel plates. Therefore, the experimental uncertainty of excess reactivity and control rod worth was finally determined to be about 3% at most by averaging the experimental data, and estimating its standard deviation, as observed in operations of the previous decade in the KUCA A-core, as shown in Table 8.2.

Table 8.1 Experimental uncertainties of HEU fuel plate (Refs. [1, 2])
Table 8.2 Measured results [pcm] of excess reactivity and control rod worth with standard deviation obtained from experimental data in EE1 and E3 cores (Refs. [1, 2])

8.2 Criticality

8.2.1 Numerical Simulations

8.2.1.1 Stochastic Calculations

Excess reactivity was numerically deduced by the MCNP6.1 code [4] with the JENDL-4.0 [5] and the ENDF/B-VII.0 [6] libraries through the difference between the critical and super-critical states in the core; control rod worth was numerically obtained by the difference between critical and subcritical states. For the evaluation of excess reactivity and control rod worth, in the critical core, the effective delayed neutron fraction (βeff) was acquired by MCNP6.1 (2,000 active cycles of 50,000 histories; 5 pcm statistical error) with JENDL-4.0. The values of βeff at critical state of EE1 and E3 cores were 831 and 805 pcm, respectively; those of the neutron generation time (Λ) were 3.027E-05 and 4.771E-05 s, respectively. Atomic number densities of core components comprise fuel elements, moderator (reflector), control rod, and Al sheath, for analyzing experimental values of excess reactivity and control rod worth.

8.2.1.2 Deterministic Calculations

Numerical analyses by deterministic calculations were performed by combining the SRAC2006 [7] and the MARBLE [8] code systems: collision probability calculations (PIJ [7]) and eigenvalue calculations (CITATION [9]) of SRAC2006, sensitivity coefficient calculations (SAGEP [10]) and uncertainty calculations (UNCERTAINTY [8, 11]) of MARBLE, coupled with the JENDL-4.0 nuclear data library. Experimental analyses of uncertainty were conducted with the use of covariance data of cross sections contained in JENDL-4.0, including uncertainty of excess reactivity and control rod worth induced by the nuclear data, and the effects of decreasing uncertainty on the accuracy of excess reactivity and control rod worth. Here, in a series of deterministic calculations, the CITATION code was notably executed for obtaining sensitivity coefficients by the SAGEP code based on the diffusion calculations.

8.2.2 Sensitivity and Uncertainty

8.2.2.1 Numerical Reactivity

The experimental values of excess reactivity (positive value) \(\Delta \rho_{\text{Excess}}^{\text{Exp}}\) and control rod worth (negative value) \(( - \Delta \rho_{\text{Rod}}^{\text{Exp}} )\) were deduced by effective multiplication factors \(k_{\text{Clean}}^{\text{Exp}}\) and \(k_{\text{Rod}}^{\text{Exp}}\) in super-critical (clean core) and subcritical states (rod insertion core) obtained by the positive period method and the rod drop method, respectively, as follows:

$$\Delta \rho_{Excess}^{Exp} = 1 - \frac{1}{{k_{Clean}^{Exp} }},$$
(8.1)
$$- \Delta \rho_{\text{Rod}}^{\text{Exp}} = 1 - \frac{1}{{k_{\text{Rod}}^{\text{Exp}} }}.$$
(8.2)

In MCNP analyses, numerical value \(\Delta \rho_{\text{Excess}}^{\text{MCNP}}\) or \(( - \Delta \rho_{\text{Rod}}^{\text{MCNP}} )\) was deduced by the difference between two effective multiplication factors \(k_{\text{Clean}}^{\text{MCNP}}\) or \(k_{\text{Rod}}^{\text{MCNP}}\) and \(k_{\text{Critical}}^{\text{MCNP}}\) in the super-critical or subcritical and critical cores, respectively, as follows:

$$\Delta \rho_{\text{Excess}}^{\text{MCNP}} = \frac{1}{{k_{\text{Critical}}^{\text{MCNP}} }} - \frac{1}{{k_{\text{Clean}}^{\text{MCNP}} }},$$
(8.3)
$$- \Delta \rho_{\text{Rod}}^{\text{MCNP}} = \frac{1}{{k_{\text{Critical}}^{\text{MCNP}} }} - \frac{1}{{k_{\text{Rod}}^{\text{MCNP}} }}.$$
(8.4)

In MCNP calculations, \(k_{\text{Critical}}^{\text{MCNP}}\) needs to be defined as the value of the effective multiplication factor in the critical core, since the numerical value is not always a unit.

On the basis of the experimental methodology shown in Eqs. (8.1) and (8.2), a numerical approach of excess reactivity \(\Delta \rho_{\text{Excess}}^{\text{CITATION}}\) and control rod worth \(( - \Delta \rho_{\text{Rod}}^{\text{CITATION}} )\) by deterministic calculations (CITATION) is generally expressed, respectively, as follows, as were experimental values:

$$\Delta \rho_{\text{Excess}}^{\text{CITATION}} = 1 - \frac{1}{{k_{\text{Clean}}^{\text{CITATION}} }},$$
(8.5)
$$- \Delta \rho_{\text{Rod}}^{\text{CITATION}} = 1 - \frac{1}{{k_{\text{Rod}}^{\text{CITATION}} }},$$
(8.6)

where \(k_{\text{Clean}}^{\text{CITATION}}\) and \(k_{\text{Rod}}^{\text{CITATION}}\) indicate the effective multiplication factors in the super-critical and subcritical cores, respectively.

Of the two numerical values by CITATION and MCNP, as mentioned in Sect. 8.2.2.1, the CITATION calculations needed to conduct a series of sensitivity and uncertainty analyses by SAGEP and UNCERTAINTY, respectively. Meanwhile, the MCNP calculations were requisite to assess the precision of eigenvalue calculations, such as eigenvalue bias [12]. That is why two numerical values were introduced by the stochastic (Eqs. (8.3) and (8.4)) and the deterministic (Eqs. (8.5) and (8.6)) approaches, and compared differently with the experimental values shown in Eqs. (8.1) and (8.2).

8.2.2.2 Sensitivity Coefficient

Sensitivity coefficient S of the integral reactor physics parameter (effective multiplication factor) R is defined by the ratio of the rate of change in R and a certain parameter x as follows:

$$S\, = \,{{\frac{dR}{R}} \mathord{\left/ {\vphantom {{\frac{dR}{R}} {\frac{dx}{x}}}} \right. \kern-0pt} {\frac{dx}{x}}}.$$
(8.7)

The effective multiplication factor keff is expressed by a balance equation of neutrons as follows:

$${\mathbf{A}}\phi = \frac{1}{{k_{\text{eff}} }}{\mathbf{F}}\,\phi ,$$
(8.8)

where A and F indicate operators of transport and fission terms, respectively, and ϕ the forward neutron flux. Multiplying Eq. (8.8) by adjoint neutron flux ϕ * and integrating over whole volume and energy, the following equation is obtained:

$$\frac{1}{{k_{\text{eff}} }} = \frac{{\left\langle {\phi^{*} {\mathbf{A}}\phi } \right\rangle }}{{\left\langle {\phi^{*} {\mathbf{F}}\phi } \right\rangle }},$$
(8.9)

where brackets < > indicate integration over the whole volume and energy.

With the use of an operator B, Eq. (8.8) is expressed as follows:

$$\left( {{\mathbf{A}} - \frac{1}{{k_{\text{eff}} }}{\mathbf{F}}} \right)\,\phi = {\mathbf{B}}\phi = 0.$$
(8.10)

Here, assuming that parameter x, operator B, and neutron flux ϕ are changed into x + δx, B + δB, and ϕ + δϕ, respectively, in a critical state, the following equations are obtained:

$$\left( {{\mathbf{B}}\, + \,\delta {\mathbf{B}}} \right)\,\left( {\phi \, + \,\delta \phi } \right)\, = \,0\,\,\,\,\,.$$
(8.11)

Neglecting second-order perturbation terms, Eq. (8.10) is expressed as follows:

$${\mathbf{B}}\,\delta \phi + \,\delta {\mathbf{B}}\,\phi \, = \,0\,\,\,\,\,.$$
(8.12)

Introducing the generalized adjoint flux Γ*, the following equation is obtained with the use of adjoint operator B* and a certain adjoint source term q*, defined as reactivity in these analyses:

$${\mathbf{B}}^{*} \,\varGamma^{*} \, = \,q^{*} \,\,\,\,\,.$$
(8.13)

Considering the theoretical background [13,14,15,16] and using Eqs. (8.10) through (8.13), the sensitivity coefficient in Eq. (8.7) is finally expressed by applying the first-order perturbation approximation [17], as follows:

$$S\, = \,\frac{{\left\langle {\phi^{*} \,\left( { - \frac{{\partial {\mathbf{B}}}}{\partial x}} \right)\,\phi } \right\rangle }}{{\left\langle {\phi^{*} \,{\mathbf{F}}\,\phi } \right\rangle }}\,k_{eff} \,\,\,\,\,.$$
(8.14)

Finally, applicability of sensitivity analyses to keff was investigated for a thermal spectrum core, such as the KUCA core, with the use of SAGEP that had been originally developed for conducting the sensitivity analyses of fast reactors.

8.2.2.3 Uncertainty

In analyzing the cross-section uncertainty of nuclear data [18], the uncertainty of reactor physics parameter ν is expressed as follows:

$$\nu \, = \,{\mathbf{G}}_{tar} \,{\mathbf{M}}\,({\mathbf{G}}_{tar} )^{{\mathbf{t}}} \, = \,\sum\limits_{i} {} \sum\limits_{j} {s_{i} \,c_{i,\,j} \,s_{j} } \, \equiv \,\sum\limits_{i} {} \sum\limits_{j} {\upsilon_{i,\,j} } \,\,\,\,\,(1 \le \,i,\,j\, \le \,p)\,\,\,\,\,,$$
(8.15)

where Gtar (1 × p) indicates the sensitivity vector of reactor physics parameters, M (p × p) the covariance matrix of nuclear reaction parameters, si the sensitivity coefficient, \(c_{i,\,j}\) the covariance, \(\upsilon_{i,\,j}\) the factor of uncertainty and p the number of nuclear reactions including the nuclides. Thus, the contribution of uncertainty ui in each nuclear reaction can be defined as follows:

$$u_{i} \, \equiv \,\sum\limits_{i} {\upsilon_{i,\,j} } .$$
(8.16)

Generally, since sensitivity coefficient si and covariance ci, j are dominant in the energy group, the factor of uncertainty is finally expressed with the use of the maximum number of energy group G as follows:

$$\upsilon_{i,j} = \sum\limits_{g} {\sum\limits_{g\,'} {s_{g}^{\,i} c_{g,\,g\,'}^{\,i,\,j} s_{g\,'}^{\,j} } \left( {1 \le g,g' \le G} \right)} ,$$
(8.17)

where g and g′ indicate the energy groups.

8.2.3 Results and Discussion

8.2.3.1 Eigenvalue Calculations

In MCNP simulations, excess reactivity and control rod worth were obtained by two eigenvalue calculations in critical and super-critical, and, critical and subcritical states, respectively: the difference between the inverse values of eigenvalue calculations in the two states. Here, MCNP eigenvalue calculations were made with 2,000 active cycles of 50,000 histories, resulting in a standard deviation within 10 pcm. The numerical results of excess reactivity and control rod worth were obtained by MCNP6.1 with JENDL-4.0 in EE1 and E3 cores, as shown in Table 8.3a, b, respectively. Moreover, estimation of C/E (calculation/experiment) values revealed an accuracy of around 5% error with the use of the experimental and numerical results of excess reactivity and control rod worth, as shown in Eqs. (8.1) and (8.2), respectively, excluding small values of excess reactivity and C2 control rod worth in EE1 core. From the calculated results in Table 8.3a, b, the difference between numerical analyses by MCNP6.1 with JENDL-4.0 and ENDF/B-VII.0 was found within an error of 3% of the C/E value.

Table 8.3 Comparison between measured and calculated (MCNP6.1) results of excess reactivity and control rod worth in EE1 and E3 cores (Ref. [1])

The ability of MCNP6.1 calculations was confirmed at a critical state in terms of the eigenvalue bias by the MCNP approach, as shown in Table 8.4. In EE1 core, eigenvalue bias by MCNP6.1 with JENDL-4.0 demonstrated a relatively small value of about 250 pcm, and with ENDF/B-VII.0 a value about 460 pcm (Table 8.4). Similarly, in E3 core, the value with JENDL-4.0 was small, about 440 pcm, compared with that with ENDF/B-VII.0, about 580 pcm. From the analyses of eigenvalue bias, a significant index of the accuracy of experimental analyses was acquired by MCNP calculations in EE1 and E3 cores at KUCA; also, as in previous studies [12, 19], JENDL-4.0 was considered reliable as a reference nuclear data library in a series of sensitivity and uncertainty analyses of excess reactivity and control rod worth in the KUCA A core.

Table 8.4 Numerical results by MCNP6.1 eigenvalue calculations in critical state (Ref. [1])

The numerical values of keff in excess reactivity and control rod worth shown in Eqs. (8.5) and (8.6), respectively, were deduced, for a clean core (withdrawal of all control and safety rods) and a subcritical core (control rod insertion) in super-critical and subcritical states, respectively, through the results of diffusion-based eigenvalue calculations (CITATION) in the 107-energy-group and x-y-z dimensions (3-D) with JENDL-4.0. Also, on the basis of accuracy of experimental analyses by CITATION (Table 8.5), sensitivity analyses of keff in excess reactivity and control rod worth were notably conducted by diffusion-based calculations (SAGEP).

Table 8.5 Comparison between measured and calculated (CITATION with JENDL-4.0) results of keff (excess reactivity: super-critical state; control rod worth: subcritical state) in EE1 and E3 cores (Ref. [1])

8.2.3.2 Sensitivity Coefficients

Sensitivity coefficients Eq. (8.7) of keff in excess reactivity and control rod worth were analyzed by the SAGEP code for assessing cross-section data of inelastic scattering, elastic scattering and capture reactions of 27Al, boron isotopes (10, 11B), carbon (12C), hydrogen (1H), oxygen (16O), and uranium isotopes (234, 235, 236, 238U) comprising the core components.

For excess reactivities in EE1 and E3 cores, the sensitivity coefficients of elastic scattering reactions were relatively highly positive, mostly 1 MeV, in 27Al, 12C, and 1H, as shown in Fig. 8.4a, and b, respectively. Sensitivity coefficients were dominant over the high-energy (MeV) region of the inelastic scattering reactions of 27Al in keff (excess reactivities) at EE1 and E3 cores shown in Fig. 8.5a, b, respectively. In thermal neutron region shown in Fig. 8.6a, b, the capture cross sections of 27Al, 1H, and 235U were highly sensitive at EE1 and E3 cores, respectively. Also, the sensitivity coefficients of 27Al, 1H, and 235U were remarkably higher in E3 core than in EE1 core ranging between 0.01 and 100 eV shown in Fig. 8.6b, because E3 core is a relatively soft-spectrum core shown in Fig. 8.3. In a series of sensitivity analyses shown in Figs. 8.4 through 8.6, effects of Al on sensitivities were observed in entire reactions and energy regions, and attributable to containing Al itself comprising of U-Al alloy (HEU) fuel plates and Al sheath of fuel assembly.

Fig. 8.4
figure 4

Sensitivity coefficients for elastic scattering reactions in excess reactivity (Ref. [1])

Fig. 8.5
figure 5

Sensitivity coefficients for inelastic scattering reactions in excess reactivity (Ref. [1])

Fig. 8.6
figure 6

Sensitivity coefficients for capture reactions in excess reactivity (Ref. [1])

Further study of the sensitivity coefficients was made of keff (worth of C1 control rod) at EE1 and E3 cores, since the worth of C1 control rod was mostly larger in both EE1 and E3 cores, compared with other reactivities shown in Table 8.3. Also, the worth of C1 control rod was selected to investigate directly the effect of the boron isotope component of the control rod. As shown in Fig. 8.7a, b, the sensitivity coefficients of 27Al, 10B, 1H, and 235U were negative in the capture reactions; among these, the capture cross sections of 27Al and 235U were highly sensitive in the thermal neutron region, as well as for capture reactions in the excess reactivity shown in Fig. 8.6a, b. Moreover, the sensitivity coefficient of 27Al was remarkably large in the E3 core with a thermal neutron spectrum, as shown in Fig. 8.7b, as was that of 235U. Finally, in C1 control rod worth, sensitivity coefficient of 10B was found relatively of negligible significance due to an insertion of C1 control rod, although that of 27Al comprising of core components (U-Al alloy fuel plates and Al sheath) was large.

Fig. 8.7
figure 7

Sensitivity coefficients for capture reactions in C1 rod worth (Ref. [1])

8.2.3.3 Uncertainty

The uncertainty analyses by the UNCERTAINTY code of the MARBLE system were conducted with the use of JENDL-4.0 covariance data (107-energy-group). Since the covariance data of 27Al, 12C, and 1H isotopes consisted mainly of core components that are not contained in JENDL-4.0, uncertainty analyses were executed for various reactions of 10, 11B, 16O, and 235, 238U isotopes comprising of control and fuel rods in the KUCA A-core, including capture, elastic scattering, inelastic scattering, fission, and (n, 2n) reactions covered in the SAGEP code. As shown in Table 8.6, the uncertainty of excess reactivity in EE1 core induced by covariance data was large, total uncertainty 135.8 pcm, compared with an experimental error of 6 pcm (Table 8.2). The value of total uncertainty was acquired through the square root of the sum of squares for reaction-wise contributions. Among the isotopes, uncertainty was dominant over the sum of all contributions, including the capture and fission reactions of 235U; a large contribution [19] was attributable to the sensitivity coefficients of 235U capture and fission reactions. For the worth of C1 control rod in E3 core, the total uncertainty was 164.1 pcm, although the reaction-wise contribution was slight in the boron isotopes, as shown in Table 8.7, demonstrating the same tendency of excess reactivity as in EE1 core shown in Table 8.6. Finally, the uncertainty of keff in excess reactivity and control rod worth (C1, C2 and C3 rods) was summarized around 150 pcm in the EE1 and E3 cores.

Table 8.6 Reaction-wise contribution [pcm] to excess reactivity induced by covariance data of JENDL-4.0 in EE1 core (Ref. [1])
Table 8.7 Reaction-wise contribution [pcm] to the worth of C1 control rod induced by covariance data of JENDL-4.0 in E3 core (Ref. [1])

Furthermore, the effect of decreasing uncertainty induced by nuclear data on calculated keff was investigated by the cross-section adjustment method [20, 21], with the use of uncertainty of keff values. The result of this investigation demonstrated a great improvement from around 150 to 3 pcm induced by nuclear data of JENDL-4.0 in all excess reactivity and control rod worth in EE1 and E3 cores. Moreover, by applying the cross-section adjustment method to the uncertainty analyses, the C/E value of all excess reactivity and control rod worth in both EE1 and E3 cores reached around a unit.

8.3 Benchmarks

8.3.1 Experimental Analyses

8.3.1.1 Reactivity Measurements

Before quantifying the uncertainty in criticality, the validity of the standard modeling of the core configuration was verified by the comparison of the excess reactivity and the control rod worth between the calculation and the experiment, without consideration of variation in the position and material property. The calculation of the reactivity was performed through two eigenvalue calculations with MCNP6.1 and KENO-VI module of SCALE6.2 code system [22] together with ENDF/B-VII.1. The calculated reactivity was obtained as follows:

$$\rho_{\text{excess}}^{\text{cal}} = \frac{1}{{k_{\text{eff}}^{\text{critical}} }} - \frac{1}{{k_{\text{eff}}^{\text{clean}} }},$$
(8.18)
$$\rho_{{{\text{rod}}\,}}^{\text{cal}} = \frac{1}{{k_{\text{eff}}^{\text{rod}} }} - \frac{1}{{k_{\text{eff}}^{\text{critical}} }},$$
(8.19)

where \(\rho_{\text{excess}}^{\text{cal}}\) and \(\rho_{\text{rod}}^{\text{cal}}\) are the calculated excess reactivity and control rod worth, respectively, \(k_{\text{eff}}^{\text{critical}}\) the keff value at the critical state, \(k_{\text{eff}}^{\text{clean}}\) the keff value at the withdrawal of all control rods and \(k_{\text{eff}}^{\text{rod}}\) the keff value at the insertion of control rod C1, C2, or C3 in the critical state.

8.3.1.2 Numerical Simulations

Through the development of the methodology of the adjoint flux [23, 24], sensitivity and uncertainty analyses were easily conducted with the use of the Monte Carlo method applying to rigorous modeling without homogenization [25]. Sensitivity and uncertainty analyses of keff induced by nuclear data were performed by TSUNAMI-3D module of SCALE6.2 together with ENDF/B-VII.1 and its 56-group covariance library (56groupcov7.1) for standard modeling of EE1 and E3 core configurations. Here, the adjoint flux was obtained by the CLUTCH method [26].

Variation in the manufacturing tolerance of HEU plates is provided by statistically processing the measured results (enrichment and thickness) of all plates at KUCA and with specification sheet in the fabrication for length of each side, as shown in Table 8.1. On the basis of the variation in HEU plates, the uncertainty analyses for the enrichment and tolerance of length of both sides were conducted with KPERT option in MCNP6.1 together with ENDF/B-VII.1. Since the variation is too small to explicitly calculate the impact (difference in keff values), a pseudo variation was considered 10%, instead of the actual variation shown in Table 8.1, in the perturbation for the enrichment and length of sides of the HEU plates. Here, while varying the length of the sides of HEU plates, their mass was maintained by retaining the original number of atoms. The pseudo uncertainty of keff attributed to varying the enrichment and length was converted to the actual one (Table 8.1) on the basis of the standard method provided in the guideline by OECD/NEA [27] as follows:

$$\Delta k_{\text{eff}} = \sqrt {\sum\limits_{i\, = \,1}^{N} {\frac{1}{{n_{i} }}\,\left( {\frac{{\Delta k_{{{\text{eff}},\,i}} }}{{\Delta q_{i} }} \cdot \frac{{\Delta q_{i} }}{{\Delta x_{i} }}} \right)^{2} } } ,$$
(8.20)

where, \(\Delta k_{\text{eff}}\) is the difference between keff values before and after variation ∆qi (the intensity of the pseudo variation), ∆xi the real uncertainty shown in Table 8.1, ni the number of HEU plates involved in the variation, finally, i and N the region of perturbation and the total number of regions, respectively. In the calculation for the variation in the enrichment and the length of HEU plates, the core was divided into fuel rod regions in the x-y plane (25 divisions in EE1 core; 21 divisions in E3 core) and into three regions in z axis (N = 75 and 63 in EE1 and E3 cores, respectively). The uncertainty of keff by varying the thickness of HEU plates was evaluated by setting all HEU plates 3.1% decreasing in thickness according to Ref. [14].

The uncertainty attributed to the reproducibility of control rod position was approximately evaluated by eigenvalue calculations (Eq. (8.20)) with MCNP6.1, and by varying control rod position (x-y directions) in the casing for 5.15 mm radially (∆qi in Eq. (8.20)) and by 8 segments circumferentially. Then, the actual uncertainty of control rod position in the x-y plane is limited to a radius of 1.15 mm (∆xi in Eq. (8.20)). In the case of one (two) control rod(s) inserted, N in Eq. (8.20) becomes 8 (64). The uncertainty was finally deduced by subtracting the keff value obtained at the reference position from that obtained by varying the position.

8.3.2 Uncertainty

8.3.2.1 Eigenvalue Bias

The eigenvalue calculations with the use of MCNP6.1 and SCALE code system were performed for a total of 1E + 08 histories (1E + 03 active cycles of 1E + 05 each); the statistical error was less than 10 pcm. Through the comparison of the results of keff between MCNP6.1 and SCALE6.2/KENO-VI, the difference was found about 100 pcm in EE1 core and about 200 pcm in E3 core, as shown in Tables 8.8 and 8.9, respectively. Moreover, eigenvalue bias was dependent on the neutron spectrum of the core: about 350 pcm and about 600 pcm in EE1 and E3 cores, respectively. Interestingly, the uncertainty induced by nuclear data showed about 950 pcm in the keff evaluation by the SCALE code. Also, the uncertainty was found almost same value regardless of the control rod position, indicating that the neutronic characteristics are the same even at insertion and withdrawal of control rods.

Table 8.8 Comparison of keff values between experiments and calculations (MCNP6.1 and SCALE6.2) in EE1 core (Ref. [2])
Table 8.9 Comparison of keff values between experiments and calculations (MCNP6.1 and SCALE6.2) in E3 core (Ref. [2])

To validate the modeling of core configuration and eigenvalue calculations, the calculated results of excess reactivity and control rod worth compared with the measured ones in EE1 and E3 cores, as shown in Tables 8.10 and 8.11, respectively. Although eigenvalue bias was smaller than the uncertainty induced by nuclear data, the comparison revealed the relative difference of 10% in C/E (calculation/experiment) values, indicating that the calculations of EE1 and E3 cores were valid and pertinently modeled for experimental analyses.

Table 8.10 Comparison between measured and calculated reactivity at critical experiments in EE1 core (Ref. [2])
Table 8.11 Comparison between measured and calculated reactivity at critical experiments in E3 core (Ref. [2])

8.3.2.2 Core Components

The impact of 235U was observed about a significant 900 pcm in both EE1 and E3 cores, as shown in Tables 8.12 and 8.13, respectively. Especially, in the EE1 core, the uncertainty was mostly composed of the values of χ, ν and (n, γ) (capture cross section) reactions of 235U that are related to the infinite multiplication factor. In fact, sensitivity profiles of the χ value of 235U shown in Fig. 8.8 were large with a large number of standard deviations. A marked difference was observed in the \(\overline{\nu }\) value of 235U shown in Fig. 8.9 between EE1 and E3 cores at thermal neutron and resonance regions in sensitivity profiles; also, core spectrum dependence on sensitivity was effectively canceled by constant standard deviation at these regions.

Table 8.12 Breakdown of the uncertainty [pcm] of keff in nuclides and nuclear reactions in EE1 core (Ref. [2])
Table 8.13 Breakdown of the uncertainty [pcm] of keff in nuclides and nuclear reactions in E3 core (Ref. [2])
Fig. 8.8
figure 8

Sensitivity profile and standard deviation covariance data for χ value of 235U (Ref. [2])

Fig. 8.9
figure 9

Sensitivity profile and standard deviation covariance data for \(\bar{v}\) value of 235U (Ref. [2])

The uncertainty of capture reactions of polyethylene with the consideration of the thermal scattering law S(α, β) (termed *1H in Tables 8.12 and 8.13) was effective in E3 core more than scattering (*1H (n, n)) reactions caused by the soft spectrum core with a large number of moderators as indicated by sensitivity profiles in Figs. 8.10 and 8.11.

Fig. 8.10
figure 10

Sensitivity profile and standard deviation covariance data for H (n, n) reactions (polyethylene) (Ref. [2])

Fig. 8.11
figure 11

Sensitivity profile and standard deviation in covariance data for H (n, γ) reactions (polyethylene) (Ref. [2])

Furthermore, the core spectrum was found to be dependent on the uncertainty of aluminum (Al) in the HEU plate (U-Al alloy) and aluminum in the core component (Al sheath) at KUCA indicated by “27Al” and “*27Al,” respectively, as shown in Figs. 8.12 and 8.13. In the EE1 core, elastic scattering and inelastic scattering (27Al (n, n′)) reactions in HEU plates affected the uncertainty because of the large sensitivity at the fast neutron region as shown in Figs. 8.14 and 8.15, respectively. Also, at the hard spectrum core, elastic scattering reactions of the Al sheath indicated higher value than that of 27Al in HEU plates. Here, uncertainty that is not varied by control rod insertion should be emphasized, because the impact of nuclear reactions related to boron are very small and not shown in Tables 8.12 and 8.13. Accordingly, the calculated results of excess reactivity and control rod worth were considered in good agreement with the measured ones within a 10% difference because the uncertainty of boron is not induced by control rod insertions.

Fig. 8.12
figure 12

Uncertainty of aluminum in HEU (U-Al alloy) plates, aluminum sheath, and control rod guide tube induced by nuclear data in EE1 core (Ref. [2])

Fig. 8.13
figure 13

Uncertainty of aluminum in HEU (U-Al alloy) plates, aluminum sheath, and control rod guide tube induced by nuclear data in E3 core (Ref. [2])

Fig. 8.14
figure 14

Sensitivity profile and standard deviation in covariance data for 27Al (n, γ) reactions (HEU plate) (Ref. [2])

Fig. 8.15
figure 15

Sensitivity profile and standard deviation in covariance data for 27Al (n, n′) reactions (HEU plate) (Ref. [2])

8.3.2.3 Tolerance of HEU Plate

For the variation in manufacturing tolerance of HEU plates shown in Table 8.1, uncertainty was evaluated with MCNP6.1 together with ENDF/B-VII.1 with the same number of histories as was reactivity evaluation, as shown in Tables 8.14 and 8.15. Based on the evaluation of the uncertainty for HEU plates, the uncertainty of the enrichment (4–14 pcm), length of sides (5 pcm), and thickness (10 pcm) was small regardless of the position of the control rods. Nonetheless, the difference of neutron spectra demonstrated its dependence on the uncertainty between EE1 and E3 cores, emphasizing especially the variation of total number of fuel plates: 3000 and 756 plates in EE1 and E3 cores, respectively. Additionally, the uncertainty attributed to variation in manufacturing tolerance was smaller than that induced by nuclear data, indicating that uncertainty induced by nuclear data is reasonable for the accuracy of criticality at KUCA.

Table 8.14 Uncertainty [pcm] of keff attributed to manufacturing variation in HEU plates in Table 8.1 and reproducibility of control rods for EE1 core (Ref. [2])
Table 8.15 Uncertainty [pcm] of keff attributed to manufacturing variation in HEU plates in Table 8.1 and reproducibility of control rods for E3 core (Ref. [2])

8.3.2.4 Reproducibility of Control Rod Position

The uncertainty induced by the reproducibility of control rod positions, as shown in Tables 8.14 and 8.15, indicated about 3 pcm even at the withdrawal (no insertion) of control rods in Cases I-1 and II-1, showing an index of accuracy induced by the approximation in Eq. (8.20). By considering the index from the control rod insertion pattern, the uncertainty attributed to varying control rod position was evaluated about 8 pcm depending slightly on the insertion pattern. Here, the evaluated uncertainty was nearly the same as the experimental uncertainty in the reactivity shown in Tables 8.10 and 8.11 (2 pcm through 11 pcm), demonstrating that the measured reactivity was slightly varied by the position of control rods.

8.4 Conclusion

Sensitivity and uncertainty analyses were conducted with the combined use of experimental results (excess reactivity and control rod worth) carried out at KUCA and numerical simulations by the MCNP6.1 calculations, the SRAC2006 and MARBLE code systems. The experimental value was compared with the calculated one by the deterministic approach with the covariance data of JENDL-4.0. Sensitivity and uncertainty analyses demonstrated that the impact of 27Al and 235U was remarkably large in the KUCA A cores, respectively. Moreover, the numerical results revealed the quantitative evaluation (about 150 pcm) of uncertainty induced by the JENDL-4.0 data library in the A cores. Also, these results indicated that further investigation is needed of the numerical analyses of uncertainty of 27Al composed mainly of core components in the A cores, with the use of 27Al covariance data, in order to assess the effect of the uncertainty of 27Al cross sections on reactivity.

To ensure the accuracy of criticality by experimental analyses at KUCA, the modeling of core configuration was examined through the comparison of excess reactivity and control rod worth between the calculation and the experiment in hard and soft spectrum cores. Furthermore, uncertainty was evaluated for manufacturing tolerance in HEU plates, for reproducibility of the control rod position, and for nuclear data. In the validation estimation of calculated keff values in the modeling of reference core materials and core configurations with MCNP6.1 and SCALE6.2/KENO-VI, the bias in calculated keff values showed that the difference in the spectrum was about 350 pcm in EE1 core and about 600 pcm in E3 core. Moreover, uncertainty of keff induced by nuclear data indicated about 950 pcm for keff evaluation with a slight variation in control rod position and core spectrum. In the breakdown of the uncertainty of keff induced by nuclear data, the impact of 235U was significantly dominant in over 90% for both cores. The sensitivities of Al in HEU plates and in Al sheaths were marked in fast neutron and resonance regions, leading to large uncertainty about 100 pcm and 40 pcm in EE1 and E3 cores, respectively. Also, uncertainty was evaluated about 10 and 8 pcm in the tolerance of HEU plates and the reproducibility of control rod positions, respectively.