Measurement of thermal neutron cross-section and resonance integral for the Ho(n,γ)Ho reaction using electron linac-based neutron source

The thermal neutron cross-section and the resonance integral of the ¹⁶⁵Ho(n,γ)^166gHo reaction have been measured by the activation method using a ¹⁹⁷Au(n,γ)¹⁹⁸Au monitor reaction as a single comparator. The high-purity natural Ho and Au foils with and without a cadmium shield case of 0.5 mm thickness were irradiated in a neutron field of the Pohang neutron facility. The induced activities in the activated foils were measured with a calibrated p-type high-purity Ge detector. The correction factors for the γ-ray attenuation (F_g), the thermal neutron self-shielding (G_th), the resonance neutron self-shielding (G_epi) effects, and the epithermal neutron spectrum shape factor (α) were taken into account. The thermal neutron cross-section for the ¹⁶⁵Ho(n,γ)^166gHo reaction has been determined to be 59.7 ± 2.5 barn, relative to the reference value of 98.65 ± 0.09 barn for the ¹⁹⁷Au(n,γ)¹⁹⁸Au reaction. By assuming the cadmium cut-off energy of 0.55 eV, the resonance integral for the ¹⁶⁵Ho(n,γ)^166gHo reaction is 671 ± 47 barn, which is determined relative to the reference value of 1550 ± 28 barn for the ¹⁹⁷Au(n,γ)¹⁹⁸Au reaction. The present results are, in general, good agreement with most of the previously reported data within uncertainty limits.     

Measurement of thermal neutron and resonance integral cross sections of the reaction V(n,γ)V using a 20 Ci Am–Be isotopic neutron source

The thermal neutron capture cross section (σ_o) and the resonance integral (I_o) of the ⁵¹V(n,γ)⁵²V reaction were measured with an activation method to provide fundamental data for reactor calculation, activation analysis, and other theoretical and experimental uses concerning the interaction of neutron with matter. The vanadium and manganese samples were irradiated within and without a Cd shield case using a 20 Ci Am–Be neutron source. The activities of the samples were measured using gamma-ray spectroscopy. The thermal neutron capture cross section and the resonance integral were determined relative to the reference reaction ⁵⁵Mn(n,γ)⁵⁶Mn and the values obtained are 5.16 ± 0.19 barns and 2.53 ± 0.1 barns respectively. The previous measurements of the σ_o and I_o of the reaction ⁵¹V(n,γ)⁵²V were reviewed and the difference between the present values and the previous results were discussed.     

Measurement of thermal neutron cross-section and resonance integral for 186W(n,γ)187W reaction by the activation method using a single monitor

The thermal neutron cross-section (σ₀) and the resonance integral (I₀) of the reaction ¹⁸⁶W(n,γ)¹⁸⁷W were measured by the activation method using ⁵⁵Mn as a single comparator. The diluted MnO₂ and WO₃ samples within and without a cylindrical Cd shield case were irradiated in an isotropic neutron field of the ²⁴¹Am–Be neutron source. The γ-ray spectra from the irradiated samples were measured by high resolution γ-ray spectrometry with a calibrated high purity Ge detector. The necessary correction factors for gamma ray attenuation, thermal and resonance neutron self-shielding effects, and the shape factor (α) for epithermal neutron spectrum were taken into account in the determinations. The thermal neutron cross-section for ¹⁸⁶W(n,γ)¹⁸⁷W reaction has been determined to be 39.5±2.3 b at 0.025 eV. This result has been obtained relative to the reference thermal neutron cross-section value of 13.3±0.1 b for the ⁵⁵Mn(n,γ)⁵⁶Mn reaction. The present value of 39.5±2.3 b for ¹⁸⁶W(n,γ)¹⁸⁷W, in general is in good agreement with most of experimental data and evaluated ones in ENDF/B-VI and JENDL-3.2 within the limits of error. The resonance integral has also been measured relative to the reference value of 14.0±0.3 b for the ⁵⁵Mn(n,γ)⁵⁶Mn monitor reaction using a 1/E^1+α epithermal neutron spectrum of the ²⁴¹Am–Be neutron source. By defining Cd cut-off energy 0.55 eV, the resonance integral obtained was 493±40 b. The existing experimental and evaluated data for the resonance integral are distributed from 290 to 534 b. The present resonance integral value agrees with some previously reported values.     

Determination of thermal neutron cross-section and resonance integral for the As (n, γ)As reaction by activation method using Mn (n, γ)Mn as a monitor

Nuclear constants for use in reactor activation analysis especially (n, γ) cross-sections and absolute gamma intensities, are known to show a rather large scatter in literature. Thermal and resonance cross-sections for the ⁷⁵As (n, γ)⁷⁶As reaction is determined by the method of foil activation using ⁵⁵Mn (n, γ)⁵⁶Mn as a reference reaction. The experimental sample with and without a cadmium cover of 1-mm wall thickness was irradiated in the isotropic neutron field of the outer irradiation sites 7 of Ghana Research Reactor-1 facility which is a miniature neutron source reactor designed by the Chinese. The irradiation channel used has a neutron spectral parameter (α) found to be (0.037 ± 0.001). The induced activity in the sample was measured by gamma ray spectrometry with a high purity germanium detector. A standard solution of Arsenic was used for the analysis. The necessary correction for gamma attenuation, thermal neutrons and resonance neutron self-shielding effects were not taken into account during the experimental analysis because they were negligible. By defining cadmium cut-off energy of 0.55 eV, the result for ⁷⁵As (n, γ)⁷⁶As reaction was found to be: thermal neutron cross-section σ₀ = (4.28 ± 0.19) b and resonance integral I₀ = (61.88 ± 1.07) b.     

Measurement of thermal neutron cross-section and resonance integral for the Yb(n,γ)Yb reaction by the cadmium ratio method

The thermal-neutron cross-section and the resonance integral for the ¹⁷⁴Yb(n,γ)¹⁷⁵Yb reaction were measured by the activation method using a ⁵⁵Mn monitor as single comparator. Analytical grade MnO₂ and Yb₂O₃ powder samples with and without a cylindrical 1 mm Cd shield box were irradiated in an isotropic neutron field obtained from three ²⁴¹Am-Be neutron sources. The gamma-ray spectra from the activated samples were measured with a calibrated n-type high-purity Ge detector. The experimental results were corrected for the correction factors calculated for thermal and epithermal neutron self-shielding effects, epithermal neutron spectrum shape and gamma-ray self attenuation. Thus, the thermal neutron cross-section for the ¹⁷⁴Yb(n,γ)¹⁷⁵Yb reaction is found to be 126.5 ± 6.6 b, relative to that of the ⁵⁵Mn monitor. The resonance integral value for the ¹⁷⁴Yb(n,γ)¹⁷⁵Yb reaction is found to be 59.6 ± 8.5 b, at cadmium cut-off energy of a 0.55 eV. Using the measured cadmium ratios of ⁵⁵Mn and ¹⁷⁴Yb, the result for resonance integral of the ¹⁷⁴Yb(n,γ)¹⁷⁵Yb reaction has also been obtained relative to the reference value of the ⁵⁵Mn monitor. The present results for the ¹⁷⁴Yb(n,γ)¹⁷⁵Yb reaction agree well only with the recent experimental ones obtained by Kafala et al. [1] and De Corte and Simonits [2] within uncertainty limits. However, the previously reported experimental data for the thermal neutron cross-section for this reaction are distributed between 24 and 141 b, and similarly the experimental values for the resonance integral value also show a large scatter in the range of 30-69 b.     

Thermal neutron cross-section and resonance integral of the Mo(n,γ)Mo reaction

We measured the thermal neutron cross-section and the resonance integral of the ⁹⁸Mo(n,γ)⁹⁹ Mo reaction by the activation method using a ¹⁹⁷Au(n,γ)¹⁹⁸ Au monitor reaction as a single comparator. The high-purity natural Mo and Au metallic foils with and without a cadmium shield case of 0.5 mm thickness were irradiated in a neutron field of the Pohang neutron facility. The induced activities in the activated foils were measured with a calibrated p-type high-purity Ge detector. The necessary correction factors for the γ-ray attenuation (F_g), the thermal neutron self-shielding (G_th) and the resonance neutron self-shielding (G_epi) effects, and the epithermal neutron spectrum shape factor (α) were taken into account. In addition, for the ⁹⁹Mo activity measurements, the correction for true coincidence summing effects was also taken into account. The thermal neutron cross-section for the ⁹⁸Mo(n,γ)⁹⁹Mo reaction has been determined to be 0.136 ± 0.007 barn, relative to the reference value of 98.65 ± 0.09 barn for the ¹⁹⁷Au(n,γ)¹⁹⁸ Au reaction. The present result is, in general, in good agreement with most of the experimental data and the recently evaluated values of ENDF/B-VII.0, JENDL-3.3, and JEF-2.2 by 5.1% (1σ). By assuming the cadmium cut-off energy of 0.55 eV, the resonance integral for the ⁹⁸Mo(n,γ)⁹⁹Mo reaction is 7.02 ± 0.62 barn, which is determined relative to the reference values of 1550 ± 28 barn for the ¹⁹⁷Au(n,γ)¹⁹⁸Au reaction. The present resonance integral value is in general good agreement with the previously reported data by 8.8% (1σ).     

Measurement of the 77Se(γ, n) cross section and uncertainty evaluation of the 79Se(n, γ) cross section

The ⁷⁷Se (γ, n) cross section was measured for the energy range from 7.6 to 13.8 MeV by using quasi-monochromatic laser-Compton scattering γ-rays. The advanced method to deduce γ-ray strength functions from (γ, n) cross section was developed. By utilizing the method, the γ-ray strength functions of ^{77, 78, 80}Se were deduced so as to reproduce the ^{77, 78, 80}Se (γ, n) cross sections measured in this work and previous systematic measurements. The inverse (n, γ) cross sections for ^{76, 77, 79}Se isotopes were calculated using the statistical model calculation code CCONE with the deduced γ-ray strength functions. The uncertainty of the calculated ⁷⁹Se(n, γ)⁸⁰Se cross section was evaluated by comparing the calculations and the experimental data on ^{76, 77}Se (n, γ) cross sections.     

Measurement of neutron capture cross-section of the Ga(n, γ)Ga reaction at 0.0536 eV energy

The neutron capture cross-section for the ⁷¹Ga(n,  γ)⁷²Ga reaction at 0.0536 eV energy was measured using activation technique based on TRIGA Mark-II research reactor. The ¹⁹⁷Au(n, γ)¹⁹⁸Au monitor reaction was used to determine the effective neutron flux. Neutron absorption and γ-ray attenuation in gallium oxide pellet were corrected in determination of cross-section. The cross-section for the above reaction at 0.0536 eV amounts to 2.75 ± 0.14 b. As far as we know there are no experimental data available at our investigated energy. So far we are the first, who carried out experiment with 0.0536 eV neutrons for cross-section measurement. The present result is larger than that of JENDL-3.3, but consistent within the uncertainty range. The value of ENDF/B-VII is higher than this work. The result of this work will be useful to observe energy dependence of neutron capture cross-sections.     

Measurement of thermal neutron cross-sections and resonance integrals for Hf(n,γ)Hf and Hf(n,γ)Hf reactions at the Pohang neutron facility

The thermal-neutron cross-sections and the resonance integrals for the ¹⁷⁹Hf(n,γ)^180mHf and the ¹⁸⁰Hf(n,γ)¹⁸¹Hf reactions have been measured by the activation method. The high purity Hf and Au metallic foils within and without a Cd shield case were irradiated in a neutron field of the Pohang neutron facility. The gamma-ray spectra from the activated foils were measured with a calibrated p-type high-purity Ge detector.In the experimental procedure, the thermal neutron cross-sections, σ₀, and resonance integrals, I₀, for the ¹⁷⁹Hf(n,γ)^180mHf and the ¹⁸⁰Hf(n,γ)¹⁸¹Hf reactions have been determined relative to the reference values of the ¹⁹⁷Au(n,γ)¹⁹⁸Au reaction, with σ₀ = 98.65 ± 0.09 barn and I₀ = 1550 ± 28 barn. In order to improve the accuracy of the experimental results, the interfering reactions and necessary correction factors were taken into account in the determinations. The obtained thermal neutron cross-sections and resonance integrals were σ₀ = 0.424 ± 0.018 barn and I₀ = 6.35 ± 0.45 barn for the ¹⁷⁹Hf(n,γ)^180mHf reaction, and σ₀ = 12.87 ± 0.52 barn and I₀ = 32.91 ± 2.38 barn for the ¹⁸⁰Hf(n,γ)¹⁸¹Hf reaction. The present results are in good agreement with recent measurements.     

Thermal neutron cross-section and resonance integral of the W(n, γ)W reaction

We measured the thermal neutron cross-section and the resonance integral of the reaction ¹⁸⁶W(n, γ)¹⁸⁷W by the activation method using a ¹⁹⁷Au(n, γ)¹⁹⁸Au monitor reaction as single comparator. The high-purity natural W and Au metallic foils with and without a cadmium shield case of 0.5 mm thickness were irradiated in a neutron field of the Pohang neutron facility. The induced activities in the samples were measured by high-resolution γ-ray spectrometry with a calibrated p-type high-purity Ge detector. The necessary correction factors for γ-ray attenuation (F_g), thermal neutron self-shielding (G_th), and resonance neutron self-shielding (G_epi) effects, and the epithermal neutron spectrum shape factor (α) were taken into account. The thermal neutron cross-section for the ¹⁸⁶W(n, γ)¹⁸⁷W reaction has been determined to be 37.2 ± 2.1 barn, relative to the reference value of 98.65 ± 0.09 barn for the ¹⁹⁷Au(n, γ)¹⁹⁸Au reaction. The present result is, in general, in good agreement with most of the experimental data and the recently evaluated value of ENDF/B-VII.0 by 5.7%. By assuming the cadmium cut-off energy of 0.55 eV, the resonance integral obtained is 461 ± 39 barn, which is determined relative to the reference values of 1550 ± 28 barn for the ¹⁹⁷Au(n, γ)¹⁹⁸Au reaction. The present resonance integral value is in general good agreement with the recently measured values by 9%. The present result is lower than the evaluated ones by 10-13%.     

Thermal neutron capture cross sections for the Sm(n,γ)Sm and Sm(n,γ)Sm reactions at 0.0536 eV energy

The neutron capture cross sections for the ¹⁵²Sm(n,γ)¹⁵³Sm and ¹⁵⁴Sm(n,γ)¹⁵⁵Sm reactions at 0.0536 eV neutron energy were measured using an activation technique based on the TRIGA Mark-II research reactor, relative to the reference reaction ¹⁹⁷Au(n,γ)¹⁹⁸Au. The activity was measured nondestructively using gamma-ray spectroscopy. Our measured values at this neutron energy are the first ones and are compared with 1/v based evaluated cross sections reported in the ENDF/B-VII and JENDL-3.3 libraries. The measured value for the ¹⁵²Sm(n,γ)¹⁵³Sm reaction is 0.28% lower than JENDL-3.3 and 0.48% higher than ENDF/B-VII. Our value for the production of ¹⁵⁵Sm is about 3% and 2.3% higher than the evaluated value with ENDF/B-VII and JENDL-3.3 at 0.0536 eV, respectively.     

Stellar reaction rate of ~(55)Ni(p,γ)~(56)Cu in Type I X-ray bursts

~(56)Cu is close to the waiting-point nucleus ~(56)Ni and lies on the rapid proton capture(rp) process path in Type I X-ray bursts(XRBs). In this work, we obtained a revised thermonuclear reaction rate of ~(55)Ni(p,γ)~(56)Cu in the temperature region relevant to XRBs. This rate was recalculated based on the recent experimental level structure in ~(56)Cu, the recently measured proton separation energy of Sp = 579.8(7.1) keV, together with shell-model calculation, and the mirror nuclear structure in ~(56)Co. The associated uncertainties in the rates were estimated by a Monte Carlo method. Our revised rate is significantly different from the recent results, which were partially based on experimental results; in addition, we found that a result in a previous work was incorrect. We recommend our revised rate to be incorporated in the future astrophysical network calculations.     

Measurement of Thermal Neutron Cross Section of 137Cs(n, γ)138Cs Reaction

A calculational model for a modified diffusion coefficient has been developed to incorporate the neutron streaming effect in heterogeneous low-density channels accurately into diffusion theory calculations. The model uses a supercell, and the axial and radial diffusion coefficients of the heterogeneous inner cell are so defined that they can reproduce Benoist's axial and radial diffusion coefficients of the supercell when the diffusion coefficient of the outer cell is given as 1/3 Σ_tr . In the case of the axial diffusion coefficient, the axial buckling effect is taken into account by modifying the neutron path length within the streaming channel in calculating the collision probabilities. This model has been applied to an RZ fast reactor Core model with a gas expansion module (GEM). By using the axial diffusion coefficient obtained with the presented model, calculational error of GEM worth was reduced to less than 1/7 compared to the formula of Rowlands and Eaton.     

Depth profiling of Mg by 2010 keV resonance of Mg(p,p′γ)Mg nuclear reaction

Studies on the characteristics of 2010 keV resonance in ²⁴Mg(p,p′γ)²⁴Mg nuclear reaction for depth profiling Mg in thin films are reported. The resonance reaction, based on the detection of characteristic 1368 keV γ-rays, enables interference free measurement of Mg down to 2 × 10²⁰ atoms/cm³ and has a probing depth of about 20 μm. The width of the resonance extracted from excitation curves for thick (>180 nm) thermally grown elemental Mg films, by SPACES is about 350 ± 50 eV. The reaction has been used to depth profile Mg in a Mg/Ti/Mg/Si film which provides interesting information on interfacial mixing involving Ti layer and the underlying Mg layer.     

Measurement of 76Se and 78Se (γ, n) Cross Sections

The (γ, n) cross sections of Se isotopes (⁷⁶Se,⁷⁸Se) were measured to supply fundamental data for estimating the inverse reaction cross section, i.e., the ⁷⁹Se(n, γ)⁸⁰Se cross section. The enriched samples and a reference ¹⁹⁷Au sample were irradiated with laser-Compton scattering (LCS) γ-rays. The excitation function of each (γ, n) cross section was determined for the energy range from each near neutron separation energy to the threshold energy of (γ, 2n) reaction. The energy point corresponding to each cross section was deduced using the accurately determined energy distribution of LCS γ-rays. Systematic (γ, n) cross sections for Se isotopes including ⁸⁰Se were compared with those calculated by using a statistical model calculation code TALYS.     

Measurement of 232Th(n,f) and 232Th(n,γ) reaction rates in thorium powder cylinder bombarded with D-T neutrons†

In order to provide reference for the evaluation of thorium parameters for the conceptual design of fusion–fission hybrid energy reactor, a dedicated integral experiment was carried out in a thorium powder cylinder bombarded with D-T neutrons. Thorium capture and fission rates in the 0° direction to the incident D⁺ beam were obtained using the activation method followed by the off-line gamma-ray technique, experimental uncertainties were ～3.1% for thorium capture rate, and were 5.5%, 8.1%, and 6.3% for thorium fission rates based on fission products ^85mKr, ¹⁴³Ce, and ⁸⁷Kr, respectively. The thorium fission rate based on ^85mKr agreed well with the simulation employing ENDF/B-VII.0 library data. The influence of the oxygen contained in the thorium oxide powder and the scattering neutrons from the experimental hall was also evaluated. MCNP simulations employing ENDF/B-Ⅶ.0, JENDL-4.0 library data agreed with experiment within uncertainties except that employing ENDF/B-Ⅶ.1 (6.0%) and CENDL-3.1 (7.9%) for thorium fission rate, while for thorium capture rate, simulation employing JENDL-4.0 agreed with experiment best. The influence of reaction channels of thorium transport medium employing different library data on the thorium reaction rates could be neglected according to the simulation. The thorium capture to fission ratio demonstrated that the fuel breeding efficiency is quite low and energy production plays a leading role under the neutron spectra in this experiment.