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REPRODUCTION COPY

,,” Evaluated -Induced Cross Sections for “5eFe to 40 MeV

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This report was preptied as an ac’count of work sponsored by an agency of the United States Covcrn- mcnt. Neither the United States Government nor any agency :hereof, nor any of their employees, ‘b nukes any warranty, exprm$ or implied, or assumes any lCSA Iiabtity or responsibility for the acL’ur- acy, mmpletcness, or usefulness of any information, apparatus, product, or process disclosed, or rep- -. resents that its usc would not infringe privately owned rights. Reference hecein to any specbic tom. mercial product, process, or semcc by trade mme, trademark, manufacturer, or otherwise, does not necessarily constitute or imply its endorsement, recommendation, .x favoring by the United .$tatcs Government or any agency thcrmf. The views and opinions of authors expressed herein do not nec- essarily state or reflect tho$c of the United States Government or any agency thereof.

UNITED STATES DEPARTMENT OF ENERGY CONTRACT W-7405 -ENG. 36 LA-8626-MS (END F-304)

UC-34C Issued:December 1980

Evaluated Neutron-Induced Cross Sections for 54?58Feto 40 MeV

E.D. Arthur P.G. Young

. . . . :.. . .—-..

m p.. . s- EVALUATED NEUTRON-INDUCED CROSS SECTIONS FOR 54>56Fe TO 40 MeV

by

E. D. Arthur and P. G. Young

ABSTWICT

Cross sections for neutron-induced reactions on 54~56Fe were calculated employing several nuclear models--optical, Hauser-Feshbach, preequilibrium, and DWBA--in the energy range between 3 and 40 MeV. Aa a prelude to the calcula- tions, the necessary input parameters were determined or ver- ified through analysis of a large body of experimental data both for neutron- and -induced reactions in this mass and energy region. Calculated cross sections as well as neu- tron and gamma-ray emission spectra were incorporated into an ENDF/B-formatted evaluation suitable for use to 40 MeV. De- tails of both the calculations and the final evaluated data files are described in this report, and extensive comparisons to experimental data are given.

1. INTRODUCTION Nuclear data needs for the Fusion Materials Irradiation Test Facility (FMIT) require evaluated neutron cross sections up to energies around 40 MeV.l Since natural iron constitutes one of the most important materials for which such data is needed, we have performed a comprehensive set of nuclear model cal- culations for neutron reactions on 54*56Fe between 3 and 40 MeV. Calculated 2 results expressed in ENDF format were joined to the latest ENDF/B-V evaluation at 3 MeV to produce a new evaluation applicable to 40 MeV. Not only does the . P present evaluation extend the Version V data to higher energies, but certain + energy balance problems occurring below 20 MeV are also corrected. Since generally little neutron experimental data, with the exception of total cross sections, exist above 20 MeV, the majority of the evaluation by

1 necessity depended upon results determined from nuclear-model calculations. In this energy range, the reaction mechanisms governing most neutron-induced reac- tions on medium-mass nuclei can be described by means of the Hauser-Feshbach statistical model,3 along with corrections for preequilibrium and direct- reaction effects. In order to use such models properly, suitable input parame- ters (e.g., optical model sets, gamma-ray strength functions, etc.) must be de- termined that are valid for use in both the mass and energy range of interest in the calculation. Our efforts to determine and verify the choice of input param- eters through use of and comparison to several independent data types are de- scribed in Sec. 11. In Sec. III we describe briefly the nuclear model codes used and present comparisons of calculated cross sections to available experi- mental data, both for neutron and proton-induced reactions. Since our efforts to express calculated cross sections, spectra, and angular distributions in ENDF/B format resulted in the adoption of some nonstandard representations, we describe in Sec. IV some of the formats used and present several examples of the evaluated data at higher energies.

II. PARAMETER DETERMINATION A. Neutron ODtical Potential The spherical optical model was used to calculate total cross sections and elastic scattering angular distributions as well as particle transmission coef- ficients for the Hauser-Feshbach portion of the calculations. For , the optical parameters used to generate such transmission coefficients must be con- strained to produce agreement with higher-energy data (total cross sections, elastic angular distributions, reaction cross sections) while reproducing lower energy information (average resonance quantities). By doing so, the double cri- teria of realistic compound nucleus formation cross sections (important at all incident energies) and reasonable behavior of the low-energy transmission coef- ficients [important in processes such as (n,2n) where low-energy neutrons are emitted] can be met. To determine such parameters, we followed the approach of Lagrange and co-workers4 in which low-energy resonance data are used to simul- . taneously supplement and constrain parameters determined from fits to data at higher energies. We chose a standard representation for the neutron optical po- . tential, that is, a real potential of the Woods-Saxon form, and an imaginary PO- tential consisting of a surface Woods-Saxon derivative form plus a Woods-Saxon volume portion and a Thomas spin-orbit term. (For more detail on the optical

2 potential, see Ref. 5.) In our determination of parameters, we included the following data: (1) total cross sections between 2 and 40 MeV; (2) s- and p-wave strength functions S0, S1, along with values for the potential scattering radius R’; (3) elastic scattering angular distributions between 6 and 14 MeV; and (4) reaction cross sections between 5 and 30 MeV. The resulting neutron parameters determined from fits to these data types appear in Table 1. Figure 1 illustrates the total cross sections calculated with these parameters compared to data available for natural iron.6-19 Below 2 MeV it was difficult to obtain reasonable fits to the data, primarily because of resonance structure that persists in the total cross section up to energies around 3-4 14eV. Optical parameters have been obtained20 that fit these data at lower energies without unphysical parameter values but these are applicable only up to 20 MeV. Since our fits covered a much larger energy range, the lower energy portion was compromised somewhat to achieve reasonable agreement over the entire energy range. The effect of this discrepancy is minimized to some extent since it occurs at the lower end of the energy range covered in the calcula- tions. Since reasonable agreement was obtained for s- and p-wave strength val- ues, this helps ensure the proper behavior of lower-order transmission coeffi- cients used in the Hauser-Feshbach calculations. Examples of elastic cross sections calculated with these parameters are compared to data21-36 between 4.6 and 25 MeV in Figs. 2-6. In Fig. 7, compar- isons are made to nonelastic cross sections37-53 below 40 MeV. Our predicted

TABLE I

NEUTRON OPTICAL MODEL PARAMETERS

r(fm) a(fm) V(MeV) = 49.747 - O.4295E - 0.0003E2 1.287 0.56

wvol(MeV) = -0.207 + 0.253E 1.345 0.47

VSo(MeV) = 6.2 1.12 0.47

WSD(MeV) = 6.053 + 0.074E 1.345 0.47

Above 6 MeV WSD(MeV) = 6.497 - 0.325(E-6) FE TOTAL CROSS SECTION

‘~ PEREY, 1972 GALLOWAY, 1967 . SCHWARTZ, 1969 CA RLSON, 1970 CIERJACKS, 1970 CARLSON, 1967 FOSTER, 1971 LARSON, 1979

Lnl cd I I I I I I I I 2“10° 10’

a BRADY, 1979 0 DECONNI NCK, 1961 o PETERSON, 1960 if’+* “ ROBINSON, 1969 + v A NGELI, 1970 x MC CALLUM, 1960 A PEREY, 1972 ‘+ @ FOSTER, 1967 ++ + C IERJACKS, 1970 +* , ❑ \ LARSON.-. .,-- 1!779.- ,“-, ‘tNai*

8“10’ 10’ NEUTRON ENERGY (MEV)

Fig. 1. Measured and calculated total cross section for iron. Experimental data are from Refs. 6-19. 4 ‘o4:- u H ILL, 1958 + KINNEY, 19’70 2 A HOLMQVI ST, 1970

5.00 MEV

4.58 MEV A +A

I I I I I I I - 1.00 0.’75 0.50 0.25 0.00 –0:25 –0:50 –0.’75– DO COS THETA (CM) Fig. 2. Measured and calculated elastic angular distributions for iron. Experimental data are from Refs. 21-23.

nonelastic cross section over-estimates new results37 available at 40 MeV that were not available for inclusion in our fit. In addition, trends in the older nonelastic data indicated a somewhat higher value when extrapolated to 40 MeV. This over-prediction in the calculated reaction cross section at 40 MeV led us to renormalize downward our calculated Hauser-Feshbach cross sections in this energy range by about 10%.

Be Charged-Particle Optical Parameters . Proton and alpha particle transmission coefficients were calculated from optical parameters based on published sets obtained from experimental data fits in the mass and energy range of interest to our calculations. We adjusted the

5 o WI LENZICK, 1965 0 WI LENZICK, 1961 X HOLMQVIST, 1969 + KINNEY, 1970 .

6.53 MEV . 1

:~”~

— o 6.00 MEV a x x x x

\k - \ v- 5.56 MEV I -1

y t 0 I I I I I I 4 Loo 0.75 0.50 0.25 0.00 –0.25 –0.50 –0.75 –1.00 COS THETA (CM)

Fig. 3, Measured and calculated elastic angular distributions for iron. Experimental data are from Refs. 23-26.

parameters to better fit various experimental data types available at low and high energies?. For , we began with the Perey54 proton optical parame- ter set. We compared the reaction cross sections calculated using these parameters to data55~56 for p + 56Fe and found an over-prediction above 30 MeV as shown by the solid curve in Fig. 8. We then added an energy dependence to the imaginary potential to produce the short-dash curve in Fig. 8, which is in better agreement with the data. We were also interested to determine how well these parameters reproduced low-energy proton data. Recently there has been interest in the behavior of re- action cross sections for cases where sub-Coulomb barrier protons are con- cerned.57 In the calculation of the 54Fe(n,np) cross section, the binding

6 “o A v HOLLANDSWORTH, 1973 + KINNEY, 1970 A HOLMQVIST, 1970 ‘J“l\ -0 a“ 8.05 MEV ? A &a A A A 4 + A z AA o u. AIAI \ v 7.55 MEW + ++

3\ 7.05 MEV

?--I ‘z~ Loo 0.75 0.50 0.25 0.00 –0.25 –0.50 –0.75 - 30 COS THETA (CM)

Fig. 4. Measured and calculated elastic angular distributions for iron. Experimental data are from Refs. 22, 23, and 27.

energy of the proton in the 54Fe compound nucleus is 4.5 MeV less than that of the neutron, leading to an incident energy range where only proton and gamma-ray emission compete. To test the low-energy behavior of these parameters, we cal- culated the 55Mn(p,n) cross section and determined that low-energy proton cross sections58~59 were reasonably described, as shown in Fig. 9. Table 11 lists the modified form of the Perey proton parameters that we obtained.

. We followed a similar approach to determine alpha-particle optical parame- ters for use in our calculations. The Lemos set60 determined from the analy- sis of 20 to 30 MeV alpha scattering in this mass region formed the basis for

7 o FERRER, 1977 x VELKLEY, 1974 + KINNEY, 1970

I 1 “o I I I I 1 i I I + 1.00 0.75 0.50 0.25 0.00 –0.25 –0.50 -0.75 –1.00 COS THETA (CM)

Fig. 5 Measured and calculated elastic angular distributions for iron. Experimental data are from Refs. 23, 28, and 29.

TABLE II

PROTON OPTICAL MODEL PARAMETERS

2xJ2Q— a(fm)

V(MeV) = 58.384 - 0.55E 1.25 0.65 .

WSD(MeV) = 13.5 - 0.15E 1.25 0.47

VSo(MeV) = 7.5 1.25 0.47

rc(fm) = 1.25

8 -o + STUART, 1962 v ANDERSON, 1957 0 COON, 1959 . 0 GURTOVOJ. 1971 x HYAKUTAKE, 1975 X YUASA, 1958 ~ ———-F!l.I,l(_)T.- - > ----1956 klEV

i=l~=/ %0+. 14.60 MEV tn

-“LA. A 14.10 MEV

i I 1 ‘z~ 1.00 0.75 0.50 0.25 0.00 –0.25 –0.50 –0.75 –LOO COS THETA (CM) Fig. 6 Measured and calculated elastic angular distributions for iron. Experimental data are from Refs. 30-36.

our parameters. Energy dependence for both the real and imaginary potential were determined by approximate fits to trends in the potential depths given by Lemos at several incident energies. Further guidance was obtained from measure- ments made at higher energies in which such energy dependence were deter- mined. We checked the applicability of the resulting optical parameters by cal-

culation of 51V(a,n) and 55Mn(a,n) cross sections 61,62 using the neutron . parameters of Table I. The results appear in Fig. 10. We did not attempt to make further tests at higher energies since in the calculations the emission of . higher energy alpha particles is influenced strongly by nonstatistical effects

that have a decreased sensitivity to the transmission coefficients used. The final adopted alpha-particle optical parameters are given in Table 111.

9 FE NONELASTIC CROSS SECTION

I I I I [ 1 I I I I f I IJ a

BRADY, 197!3 MAC GREGOR, 1958 FLEROV, 1956 DEGTYAREV, 1961 MAC GREGOR, 195’7 4’ @ STRIZHAK, 195’7 + GRAVES, 1955 C3 LEBEDEV, 1958 m WALT, 1955 El BEYSTER, 1955 )( MACHWE, 1959 v TAYLOR, 1955 o PASECHNI K, 1955 + BEYSTER, 1956 0 STRIZHAK, 1956 A A BRAMOV, 1962 x MORRISON, 1956

0 I I 1 I 1 I I I I I I 1 J -1 I I I i 1 I 1 I I I 2“10° 10’ NEUTRON ENERGY (MEV)

Fig. 7. Measured and calculated nonelastic cross sections for iron. Experimental data are from Refs. 37-53.

TABLE III

ALPHA OPTICAL MODEL PARAMETERS

r(fm) a(fm)

V(MeV) = 193 - 0.15E 1.37 0.56

w“ol(MeV) = 21+0.25E 1.37 0.56

rc(fm) = 1.4 , , I I I p+ 56Fe BG I

.

0.6 1 J 1-

‘;~ 10 20 30 40 Ep(MeV)

Fig. 8. Calculated p + 56Fe reaction cross sections compared to experimental data (Refs. 55 and 56). The solid curve results from the parameters of Perey, 54 the long-dashed curve from the parameters of Becchetti,168 and the short- dashed curve from our parameters.

c. Gamma-Ray Strength Functions and Transmission Coefficients Gamma-ray emission can be an important competitor to particle emission, particularly around reaction thresholds. We chose to calculate gamma-ray trans- mission coefficients through use of gamma-ray strength functions determined from fits to cross sections. 63 This method avoids many of the problems that occur when the normalization of gamma-ray transmission coeffi- cients is determined directly from the ratio of the average gamma width, , and the s-wave resonance spacing, , as is often done in these types of calcu- lations. Such and ~> values are not always reliable, especially in the present case where information needed for compound systems away from the line of stability must be inferred from the systematic behavior of such quanti- ties. Gamma-ray strength functions should be more reliable since their behavior is expected to vary slowly between nearby nuclei. 64 For this problem, we det- ermined gamma-ray strength functions through fits to 54Fe and 56Fe capture

11 ● I I 1 I

00—

Io—

I 1, I I I 2 3 4 5 Ep (MeV)

Fig. 9. Measured and calculated cross sections for the 5~n(p,n) reaction. Experimental data are from Refs. 58 and 59.

data65S66 below 1 MeV. A giant dipole resonance shape was used along with pa- rameters determined from photonuclear data. Only El transitions were consid- ered. Some of our preliminary Hauser-Feshbach calculations of photon production - spectra indicated an improvement in the agreement of the calculated spectra to the experimental results if a 45% reduction in the tail of the Lorentz curve used to represent the giant dipole resonance was made below &y = 9 MeV. This alteration was also included in the form assumed in the determination of the

12 I.0 I I .

55 Mn(a,n)

b

n Q 7

0.1 I I I o 5 10 15 o 5 10 15 Ea(MeV) Fig. 10. Measured and calculated cross sections for the 5Wn(a,n) and ‘lf?(a,n) reactions. Experimental data for the two reactions are from Refs. 61 and 62, respectively.

strength function. The normalizing constants obtained for the strength func- tions through fits to 54Fe(n,Y) and 56Fe(n,y) data were essentially identi- cal, differing only by about 5% even though the 54Fe capture cross section is about 50% higher than that of 56Fe. Since gamma-ray production spectra were of interest along with cross sec- tions for the production of isomeric states, we employed a detailed gamma-ray cascade model in our Hauser-Feshbach calculations. In addition to El transi- tions, we allowed gamma-ray emission by Ml and E2 transitions, which were norma- lized to the El component through use of the Weisskopf estimate. A giant dipole resonance form was also assumed for these transitions. D. Discrete Levels and Level-Density Parameters The inclusion of a large number of discrete levels (where reliable experi- mental data exist) is advantageous in these calculations since such level infor- . mation results in more reliable cross sections, particularly around reaction thresholds. Such level data also provide constraints to ensure a reasonable be- . havior of level-density parameters at lower-excitation energies. We took level information-- energies, spins, parities, and gamma-ray branching ratios--from the compilation of Lederer and Shirley. 67 A listing of the discrete levels used appears in Appendix A. To represent the continuum excitation energy region occurring above the last discrete level, we used the Gilbert-Cameron68 level-density model con- sisting of Fermi-gas and constant temperature portions. For the Fermi-gas part, we generally used the level-density parameters, a, and pairing energies~ ~, given by Cook.69 The constant temperature parameters were adjusted to produce agreement with the cumulative number of available discrete levels while joining smoothly to the Fermi-gas expression at an excitation energy, Ux. BOth Fermi-gas and constant temperature parameters appear in Table IV.

E. Preequilibrium Model and Parameters Reaction mechanisms other than those described by the Hauser-Feshbach sta- tistical model begin to have important effects on neutron cross sections and spectra at higher energies. As part of the corrections to the statistical model results, we applied the preequilbrium model based on the master equations method of Kalbach.70 In this model , rates involving transitions between particles and holes are directly proportional to the square of the absolute value of the ma- trix element describing two-body residual interactions. The form for the square of the matri~ element has been recently parameterized by Kalbach71 from fits to higher energy -induced reaction data as

M2 = kf(s) . (1) A3 E Here c is the excitation energy available per exciton, E/n, and f(e) represents a function valid for different ranges of s. We used a normalization constant of .k = 160 MeV3 and the single-particle state densities were taken to be equal to Ai/13 where Ai is the mass of the ith residual nucleus. We also included pairing effects in the calculation of excitation energies that may account for

14 TABLE IV

LEVEL DENSITY PARAMETERS

I . a A E T u (MeV) (Me;) (MeV) ~- Nucleus (MeV-l) &

48Cr 6.587 2.79 -1.379 1.255 5.297 49cr 6.563 1.35 -0.354 1.239 7.104 5ocr 6.545 2.89 0.217 1.367 10.472 51cr 6.442 1.35 -1.098 1.358 8.585 52Cr 6.154 2.65 1.069 1.29 8.368 53cr 6.501 1.35 -0.491 1.272 7.456 5% 6.293 1.54 -0.91 1.383 8.844 52Mn 6.178 0.0 -1.379 1.255 5.297 53m 5.874 1.3 -1.154 1.463 8.846 54m 5.85 0.0 -2.173 1.432 7.047 55m 6.665 1.27 -0.82 1.282 7.813 56M 7.233 0.0 -2.176 1.214 6.505 51Fe 6.054 1.54 1.273 2.226 2.028 52Fe 6.015 3.08 1.142 1.366 9.563 53Fe 5.888 1.54 -0.357 1.385 8.019 54Fe 5.568 2.84 0.322 1.535 10.686 55Fe 5.909 1.54 -1.574 1.538 10.297 56Fe 6.355 2.81 -0.224 1.447 11.712 57Fe 6.923 1.54 -1.587 1.366 9.862

The quantities above are defined as: a = Level density parameter of the Fermi-gas level density expression. . A= Pairing energy. E. and T = Constant temperature level density parameters. U__= Matching energy at which constant temperature and Fermi-gas expressiona are x joined. the slight difference in our value for k over that recommended by Kalbach, namely, k = 135 MeV3. In addition to preequilibrium effects, we also included for (n,a) reactions contributions from pickup and knockout processes as described in a series of phenomenological expressions derived by Kalbach.70 These contributions, in fact, produce most of the cross sections for the (n,a) reaction and allow alpha-particle emission to be calculated without use of quantities such as alpha-particle preformation constants. The prequilibrium model as it is generally used does not include angular momentum effects so we assumed that the spin distribution of the preequilibrium components would be the same as that obtained from the equilibrium Hauser- Feshbach calculations. This approximation becomes worse as one goes to higher incident energies where preequilibrium effects dominate in the emission of par- ticles from the first compound nucleus. However, since parameters for the pre- equilibrium model have in general been determined through the analysis of charged-particle experimental data measured at energies of tens of MeV, the po- tential effect of such problems may have been lessened through the phenomenolog- ical parameter values obtained. In addition to providing corrections to calculated spectra and cross sec- tions, calculated preequilibrium fractions were also used in conjunction with phenomenological expressions for secondary particle angular distributions deter- mined from fits by Kalbach and Mann72 to particle-induced reaction data. Their analysis led to the following expression for the doubly differential cross section:

8 8 d2 o ~ao(MSD) ~ bgPL (cos13)+ ao(MSC) ~ bgP2 (cosO) . (2) dedQ !L=O 2=0 A!?=2

Here aO(MSD) and aO(MSC) refer to fractions of the preequilibrium cross section resulting from multistep direct (MSD) and multistep compound (MSC) contributions. In our calculations, the multistep direct fraction could be approximated through use of the total preequilibrium cross section, and the multistep compound was approximated by using the evaporation portion of the cross section. The Legendre coefficients, b2 , appearing in Eq. (2) were found in Ref. 72 to be essentially dependent only on the energy of the emitted particle,

2g+l ““(3) b~ = 1 + exp [AL(Bfi-S)] ‘

where A and B depend only on 2. !?, !?

F. The Direct Reaction Model and Parameters The preequilibrium and Hauser-Feshbach statistical models are not adequate to fully describe the excitation of low-lying collective states in 54$56Fe through neutron inelastic scattering since strong direct reaction processes are involved. The lower-order terms involving a small number of particle-hole pairs in the preequilibrium model can approximate in a crude manner the direct reac- tion process and for this reason the exciton or geometry-dependent hybrid models have sometimes been used to account for such direct effects in particle emission spectra. We chose, however, to perform Distorted Wave Born Approximation (DWBA) calculations to describe the excitation of collective states through the direct reaction mechanism. We used the DWBA program DWUCK73 along with the neutron optical parameters of Table I. Observed differential cross sections can be related to ones obtained from the DWBA calculation by

do 2 6: U;W(0) , (4) at= I I where is the Clebsch-Gordon coefficient (in this case) for scattering on a spin zero target nucleus. The deformation parameters f3gwere taken from 74 54 values determined by Mani from analysis of proton inelastic scattering on Fe 56 and Fe. Table V lists the states for which DWBA calculations were made along with the I? parameters used. 2 The direct cross sections obtained for the levels appearing in Table V were combined with Hauser-Feshbach calculations after the total compound nucleus formation cross section was renormalized to account for the direct reaction contributions. Because of the ambiguity as to the amount of the direct reaction process accounted for in the preequilibrium model, preequilibrium corrections were not applied to states having calculated DWBA cross sections. In these cases, only the DWBA and compound nucleus contributions were combined to produce a total cross section for such a state. 17 TABLE V

DWBA PARAMETERS USED TO CALCULATE DIRECT INELASTIC SCATTERING FROM 54,56Fe Levels

54Fe Ex(MeV) Jm

1.408 2+ 0.18 2.538 4+ 0.05 2.950 6+ 0.02 2.959 2+ 0.098 3.166 2+ 0.052 3.295 4+ 0.033 3.834 4+ 0.052 4.048 4+ 0.024 4.265 4+ 0.045 4.579 2+ 0.026 56Fe

0.846 2+ 0.22 2.085 4+ 0.03 2.658 2+ 0.06 2.960 2+ 0.02 3.123 4+ 0.087 3.370 2+ 0.06 3.388 6+ 0.037 3.602 2+ 0.05 3.755 6+ 0.04 3.832 2+ 0.03 4.120 4+ 0.045 4.298 4+ 0.04 4.401 2+ 0.05 4.510 3- 0.1 4.612 2+ 0.055 4.740 2+ 0.05 4.880 2+ 0.05

.

18 III. CALCULATED RESULTS AND DATA COMPARISONS A. Nuclear Models and Codes The cross sections presented here result from application of the basic models discussed earlier-- optical, direct reaction, preequilibrium, and Hauser- Feshbach. To generate total cross sections , shape elastic angular distribu- tions, and particle transmission coefficients , we used the spherical optical code SCAT275 with the parameters of Tables I, 11, and 111. As mentioned in Sec. 11 F, the DWBA code DWUCK73 was used to calculate direct reaction cross sections for inelastic scattering from collective levels in 54Fe and 56Fe.

For the Hauser-Feshbach portion of the calculations , we relied on the COMNUC76 and GNASH77 codes, both of which include angular momentum and parity conserva- tion explicitly. The COMNUC code was generally used for neutron energies below 4-5 MeV, since it contains a complete treatment of width-fluctuation corrections needed for accurate cross-section calculations at low energies where only a few channels are open. At higher energies, the GNASH multistep Hauser-Feshbach code was used since it includes preequilibrium corrections and can handle complex de- cay chains involving up to eight compound nuclei. Figure 11 illustrates a used for cross section calculations at higher incident neutron energies. Such detail is required since it is necessary to follow the production and decay of compound nuclei formed not only by successive but also by multiple proton emission. A summary of the important reaction cross sections obtained from the calcu- lations is given in Fig. 12. That it is important to follow the decay of pro- ton emission products is clearly shown. For example, Fig. 12 illustrates that processes involving complex chains such as (n,2np) (sum of n,p2n + n,npn + n,2np) become important and actually begin to dominate when compared to reac- tions involving only neutron emission. This occurs because these cross sections are produced by sequences involving several paths and also because the compound systems produced at higher energies tend to become more proton rich. Gamma-ray production cross sections and spectra were required at all incident neutron en- ergies, which meant that the decay sequences also had to include gamma-ray deex- . citation of nuclei populated in all major reactions.

. B. Inelastic Scattering and Neutron Emission Comparison to data available for inelastic scattering to discrete final states presents an opportunity to check several aspects of the calculations. 19 56Mn A~53cr*53cr~56Mn

~n/’’~%5,n&52CrCr

55Mn &55Mn 55~&55~e

Fig. 11. Schematic diagram of the reaction chains for n + 56Fe that was included in the calculation.

Lo

0.1

z x

0.01

0.001 10 20 30 40 En(MeV)

Fig. 12. Composite of n + 56Fe cross sections that resulted from the calculations. 20 FI+54(N,NPR1ME) EX=l.408MEV

‘o I 1

A 130SCHUNG, 1971 + KINNEY, 1974 ‘\ ‘\,

I 1 1 I I I I I I I I I I I I I I I I I I 10’ NEUTRON ENERGY (IvlEV) Fig. 13. Calculated and measured excitation functions for the 54Fe(n,n’) reaction to the 1.408-MeV level in 54Fe. Experimental data are from Refs. 78 and 79.

For low energies the calculated cross sections depend on the suitability of the neutron optical parameters used to provide transmission coefficients for the Hauser-Feshbach model, the width-fluctuation corrections and, where applicable, the results of DWBA calculations. We compare in Figs. 13 and 14 calculated excitation functions for inelastic scattering to discrete states of 54Fe meas- ured78}79 between 3 and 10 MeV. Similar results23~79-89 are shown in Figs. 15-18 for discrete states in 56Fe. The agreement indicates a proper choice of neutron optical parameters both for use in the compound nucleus calculation and also within the DW8A calculation of direct contributions. Further tests of the calculated direct cross section appear in Fig. 19 where comparisons are made to

21 FIZ-54(N,NPR1ME) EX=2.538+2.561IifEV

I I I I I I [ I I I I

/+

g:. - w’ 1-J

z o z

H(y-q w $?=~ m o (x CJ

y ~ A BOSCHUNG, 1971 + KINNEY, 1974 ‘o ~ - +- - I I I I I I I I I I I I I I 1 I I I I I I ho 10 10’ NEUTRON ENERGY (MEV)

Fig. 14. Calculated and measured composite excitation functions for the 54Fe(n,n’) reactions to the 2.538- and 2.561-MeV levels in 54Fe. Experimental data are from Refs. 78 and 79.

‘n + angular distributions34$g0 measured for excitation of the 0.846-MeV, J = 2 state in 56Fe by 14.1-MeV neutrons. Here compound nucleus contributions are minimal with the neutron optical parameters as used in the DWBA calculation pro- viding the major effect. In this energy range there exist several measurements of the neutron emis- . sion spectrum, and these are compared to our calculated results in Figs. 20-22. In Fig. 20, the angle-averaged results of Hermsdorf,91 Lukyanov, 92 and Vo- nach93 and the 90-degree measurement of Clayeux94 are compared to the cal- culated spectrum at 90 degrees. In Figs. 21 and 22, measurements at 4 angles between 35 and 145 degrees by Kammerdiener95 are compared to the calculations.

22 FE–56(N,NPRIME) EX=O.847MEV

I I I I I I I [ I [ I I

iwrrRoN ENERGY (MEV)

Fig. 15. Calculated (above 3 MeV) and measured excitation functions for the 56Fe(n,n1) reaction to the 00847-MeV level in 56Fe0 Experimental data are from Refs. 23, 79-87.

These comparisons illustrate the importance of preequilibrium effects on the spectrum and confirm the choice of the preequilibrium parameters used. In Sec. 11. E, we described a set of phenomenological expressions72 for the angular distributions of particles populating a continuum of secondary ener- gies. These expressions were derived generally from fits to higher energy . particle-induced data and have not been tested at lower energies of interest to . many neutron applications. At 14.1 MeV, the secondary neutron angular distribu- tions measured by Hermsdorf91 provide data for such a test and are compared in Fig. 23 for a series of secondary energy ranges. While some discrepancies

23 FE–56(N,NPRIME) EX=2.085NIEV

I I I I I I I I I I I

+

1’

gz: : A z o F UN la ‘- I

❑ BOSCHUNG, 19’71 + DEGTYAREV, 196’7 x MEYERHOF, 1962 A KARDASHEV, 1962 @ GI LBOY, 1965 ● HOPKINS, 1964 @ ANTOLKOVIC, 1966 v KiNNEY, 1970

I I I I I I I I I 1 1 I I I I I 10: \ NEUTRON ENERGY (MEV)

Fig. 16. Calculated and measured ex~itation functions for the 56Fe(n,n’ ) reaction to the 2.085-MeV level in ‘bFe. Experimental data are from Refs. 23, 79, 82, 83, and 85-88.

exist, the over all agreement is reasonable. Since these parameters were deter- mined principally from higher energy data, their applicability should increase at the higher incident energies of this calculation.

c. (n,2n) Cross Sections The comparison to (n,2n) data provides the opportunity to evaluate the be- havior of the low energy neutron transmission coefficients as well as to test, indirectly, effects from competing reactions involving mainly proton and gamma- ray emission. Furthermore, the calculated cross section from threshold to sev- eral MeV above threshold results principally from transitions to discrete final

24 FE–56(N,NPRIME) EX=2.658MEV

I I I I I I I I I I I .

A 4 . b –- 1 ‘w+ I n+- - A m ‘‘t

z 0 z c.) la (72 (ZJO CL?+: : !D g BOSCHUNG, 19’71 + DEGTYAREV, 1967 A KARDASHEV, 1962 * HOPKINS, 1964 8 GILBOY, 1965 al A NTOLKOVIC, 1966 v KINNEY, 1970 y o I I I I ! I I i I J I 1 I 1 1 I I I I I I ’10° 101 NmwoN ENERGY (MEv)

Fig. 17. Calculated and measured excitation functions for the 56Fe(n,n’) reaction to the 2.658-MeV level in 56Fe. Experimental data are from Refs. 23, 79, 82, 83, and 85-87.

states in the residual nucleus. Thus, neutron transmission coefficients can be tested without complications from level-density effects. Two types of iron (n,2n) data exist-- the first from scintillator tank mea- surements on natural iron and the second from activation measurements of the 54Fe(n,2n) cross section. The tank measurements on natural iron provide data . mainly about the 56Fe(n,2n) reaction where, in the case of the 56Fe compound

. nucleus, neutron and proton separation energies are essentially equivalent and neutron emission dominates. In this case, calculations are sensitive to the neutron transmission coefficients and, around threshold, to the amount of gamma-ray competition included. As described in Sec. II C., we used the gamma- 25 + I I I I I I I I I I I I *m[() [ 1 I I I 1 I I I —.10 10’ NEUTRON ENERGY (MEv) Fig. 18. Calculated and measured composite excitation functions for the 56Fe(n,n’) reactions to the 2.942- and 2.960-MeV levels in 56Fe. Experimental data are from Refs. 87 and 89.

ray strength function method to provide the normalization for the gamma-ray transmission coefficients occurring in the problem. In the case of the 56Fe compound system, values of the s-wave resonance parameters and @> are not available experimentally and would have to be determined from systematic if gamma-ray transmission coefficients were normalized to the,2m ratio, . which would lead to an increased probability for error. The use of gamma-ray strength functions should alleviate such problems, and the (n,2n) cross section . around threshold provides data to test this assumption. Figure 24 compares the 96 calculated (n,2n) cross section for natural iron to measurements by Frehaut

26 I I I I I I I I n+SGFee56Fe*(0.846MeV En=14.1 MeV 0.0

n k \ n

~ \ b m

I 0.00 i I I I I I I 20 40 60 80 I00 I 20 I 40 160 180 &J deg ) Fig. 19. Calculated and measured angular distributions for the 56Fe(n,n’ ) reaction to the 0.846-MeV level for 14.1-MeV incident neutrons. Experimental data are from Refs. 34 and 90.

and Veeserg7. The threshold agreement confirms both the gamma-ray transmis- sion coefficient normalization as well as the neutron transmission coefficient behavior. Some disagreement occurs with the Veeser data at higher energies, but this is generally less than 8%. A quite different situation exists for the 54Fe(n,2n) reaction. In the 54Fe compound system, the binding energy of the proton is about 4.5 MeV less than that of the neutron so that the probability of neutron emission is de- creased and the effect of the competing (n,np) reaction becomes more important. . Figure 25 compares our calculation to several measurements98-109 of this cross section. The fact that reasonable agreement is obtained for this cross section, . which represents less than 10% of the total reaction cross section, indicates the suitability of the parameters used to describe the competing reactions that dominate.

27 EN = 9.1 MEV THETA = 90 DEG T ~ 1 1 1 I 1 1 I -i

1975

‘&H—H+td 0.00 125 2.50 3.75 5.(XI 625 7.50 8.75 10.00

EN = 14.4 MEV THETA = 90 DEG

+ HERMSDORF, 1974 ) x LUKYANOV, 1975 0 VONACH, 1980 A CLAYEUX, 1972

+

I I t I ! 1 I \ 1 1 1 I 1 1 1.0 2.0 4.0 6.0 8.0 10.0 12.0 14.0 LO NEUTRON ENERGY (MEV) . Fig. 20. Calculated neutron emission spectra at 90 degrees for 9.1- . and 14.4-MeV neutrons incident on iron compared to the meas- urements of Refs. 91-94. The data shown for Hermsdorf,91 Lukyanov, 92 and Vonachg3 have been averaged over several angles.

28 EN = 14.93 MEV THETA = 35 DEG 7

. ~~

.

i

EN = 14.53 MEV THETA = 65 DEG 7 L , dJ- 1 t 1 1 b 1 1 4

& + KAMMERDIENER, 1972 \y m o_ - --1- - t

z 0 R CJ M m my rno_ _ 0+: : c1 u

y o- - *T’- 1 I I N 0.0 2.0 4.0 6.0 8.0 10.0 12.0 14.0 16.0 NEuTRoN ENERGY (MEv) .

Fig. 21. . Calculated neutron emission spectra at 35 and 65 degrees com- pared to Kammerdiener’s95 iron measurements near 14 MeV.

29 EN = 13.88 MEV THETA = 105 DEG T ~ 1 1 I I 1 8 1 -4-J

1972

, ,

q EN = 13.36 MEV THETA = 145 DEG

-r

z & + KAMMERDIENER, 1972 L“ m 0. _ -s+- -

z 0 ~ m m

C)

la -. + I I 1 1 , 1 1 1 I 1 *N ~. ;0 ;0 6.0 6.0 10.0 12.0 14.0 lA.O NEUTRON ENERGY (h4EV) .

. Fig. 22. Calculated neutron emission spectra at 105 and 145 degrees com- pared to Kammerdiener’s75 iron measurements near 14 MeV.

30 I I I [ I I 2-3 hleV , 20

h ‘‘~

10

0 1 I I I I I

4 8-9 MeV

2

0

b 2-II MeV 80

60

40 L I I I I 1 I 40 80 120 160 ec.m.(deg)

. Fig. 23. Calculated angular distributions of emission neutrons from 14.6- . MeV neutron interactions with iron compared to Hermsdorf’s measurementsgl for several secondary energy ranges.

31 I I I I I I I I I I I 1

Fe(n,2n)

I_t

1 I 1 I I I I I 1 I 1 10 12 14 16 [8 20 22 En(MeV)

Fig. 24. Comparison of calculated i~on (n,2n) cross sections with the scintillation tank measurements of Frehaut96 (circles) and Veeserg7 (triangles).

D. (n,p) Reactions and Proton Emission Seve”ral data types exist involving proton emission from iron that provide oppotiunities to test proton transmission coefficients calculated with the parameters of Table II. Figures 26 and 27 compare calculated (n,p) cross sections for 54Fe and 56Fe to data 102,106,107,110-137 measured for these reactions. The 54Fe(n,p) theoretical curve of Fig. 26 was obtained after a 4% reduction was made in the Fermi-gas level-density parameter, a, over that norm- . ally obtained from the Cook systematic. 69 However, this reduction made little difference in the calculation below 10 MeV as more than 90% of the cross . section was obtained from transitions to discrete levels in 54Mn or to the re- gion of the continuum described by the constant temperature level-density ex- pression. Both sets of calculations for the 54Fe and 56Fe(n,p) reactions

32 FE–54(N,2N)CROSS SECTION

I i 1+t z o t R CJ w UI + @ CHITTENDEN, 1961

❑ CROSS, 1963 x RAYBURN, 1961 v CA RLES, 1963

0 SALISBURY, 1965 x ALLA N, 1957 A SIGG, 1975 + + RYVES, 1978 1 I I 10’ NEUTRON ENERGY (MEV)

Fig. 25. Calculated and measured 54Fe(n,2n) cross sections. The experimental results are from Refs. 98-109.

agree reasonably well with the data, although perhaps better agreement could be obtained if some adjustment was made in the proton optical parameters to reduce slightly the amount of lower-energy proton emission. This adjustment was not attempted because of the possible effects on the higher-energy behavior of the proton transmission coefficients, which were checked by calculations of higher energy proton reaction data (see Sec. III B). Recently new data for the total proton-production cross section induced by 15-MeV neutrons have been obtained by measurements of the spectrum and angular distribution of the emitted protons. 138 At 15 MeV this total measured spec- trum is a sum of contributions of (n,p), (n,pn), and (n,np) reactions, thus pro- viding a further test of the behavior of proton transmission coefficients.

33 FE–54(N,P) CROSS SECTION 00 t I I 1 # I 1 1 n 1 1 I

I M BARRALL. 1968 v SINGH, 1972 o STOREY, 1960 0 ALLAN, 1961 x PAULSEN, 1979 A LAUBER. 1965 /’! SMITH, i973 ~ , ,+, ! I 1 I I ! I 1 1 I 1 I b 1 1

00 1 t 1 1 1 1 1 1 I , # 1

+

\] \ -1 \ 4 + o BARRALL, 1969 H CROSS, 1963 v RAO, 1967 o ALLAN, 1957 b 0 CROSS, 1962 x CARROLL, 1964 E CARROLL, 1965 A VAN LOEF, 1961 + SALISBURY, 1965 \ I I ! I I 1 1 I 1 1 I I 1 f I I I I i , 1 0 NEUTRON ENERG;O;MEV) . Fi . 26. Calculated and measured 5fFe(n,p) cross sections. The experimental data are from Refs. 102, 106, 107, 11O-122.

34 FE–56(N,P) CROSS SECTION

‘$ 1$

@ CHITTENDEN, 1961

o ALLAN; 1957 X CROSS, 1962 + ❑ * LISKIEN,1965 A LISKlEN,1966 q H* + SMITH, 1973

1 , # 1 ! 1 I 1

I 4

o x +-l A 1/ + q-&-+H-* NEufr#O; ENERGY (MEV)

I?i. 27. Calculated and measured 58Fe(n,p) cross sections. The experimental results are from Refs. 99, 100$ 1029 105s 107s 110-114, 117, 122-137.

35 I

I I I I I I I “+54Fe~p+x En .15Mev + . Io+; . : z \ ~ 10-2 . w u % w I0-3~ t:

10-4 1 I I I I 1 I o 2 4 6 8 10 12 14 Ep (MeV)

Fig. 28. Calculated and measured138 proton emission spectra from 15-MeV neutron interactions with 54Fe.

Effects resulting from the relative preequilibrium correction applied to the emission of protons can also be tested, since for the (n,p) and (n,pn) reactions at higher energies a large portion of these cross sections originates from the preequilibrium mechanism. Figures 28 and 29 show the calculated proton emission spectra produced by 15-MeV neutron interactions with 54Fe and 56Fe along with the measurements of Grimes et al.138 The low energy portion of the 56Fe emission spectrum is in good agreement with the data and arises from the emission of low-energy protons from the (n,np) reaction. The agreement at the higher energy portion of . the spectrum illustrates the validity of the preequilibrium corrections. For . 54Fe there is an even larger contribution from the (n,np) process; however, the large size of the (n,p) contribution to the emission spectrum prevents the occurrence of an explicit dip in either the measured or calculated spectrum.

36 o 2 4 6 8 10 12 Ep (MeV)

Fig. 29. Calculated and measured138 proton emission spectra from 15-MeV neutron interactions with 56Fe.

E. (n,a) Reactions and Alpha-Particle Emission Alpha-production data for iron isotopes include measurements of the 54Fe(n,a) cross sections below 19 MeV, which are supplemented by recent meas- urements of secondary alpha-particle spectra induced by 15-MeV neutrons on 54Fe and 56Fe. Theoretical calculations for comparison to such data present some difficulties in that there exists much less information concerning alpha-particle optical parameters needed to produce transmission coefficients applicable at lower energies. Furthermore, the mechanism for (n,a) reactions at higher energies seems not to be well described by either the statistical or pre- equilibrium models unless, for the latter case, assumptions are made concerning alpha-preformation constants or phenomenological descriptions of other reaction mechanisms are included. For these calculations we used, in addition to the Hauser-Feshbach and preequilibrium models, empirical expressions developed by Kalbach70 to describe pickup and knockout contributions to the (n,a) cross

37 FE-54(N,ALPHA) CROSS SECTION

-i’ (+ o

E

z o -1u I t

B CHITTENDEN, 1961 ❑ MASLOV, 1972 x SINGH, 1972 V CROSS, 1963 0 RAO, 1967 0 POLLEHN, 1961 x CROSS, 1962 A PAULSEN, 1979 + SA LISBURY, 1965 I I I I I t I I I 1 1 1 I 1 1 J I NEuTRoN ENERGY (MEV)

Fig. 30. Calculated and measured 54Fe(n, a) cross sections from 3-40 MeV. Experimental results are from Refs. 100, 102, 105, 106, 112, 115, 118, 122, and 139.

section. These expressions were generally developed from higher-energy reaction data, and the present calculations provide a further opportunity to examine their applicability by comparison to neutron experimental data at lower incident energies.

Figure 30 compares the calculated 54Fe(n,a) cross section to data avail- able between 1 and 19 MeV.100>102g105~106,112, 115,118,122,139 The sparsity of . the data makes definite conclusions difficult concerning the models or parame-

ters used in the calculations. The calculated results are lower than some of . the data at 14-15 MeV but the total alpha-production cross section (75 mb) is in good agreement with the value of 79 ~ 13 mb determined by integration of the

38 spectrum measured by Grimes et al.138 Our results are compared to Grimes’ measured alpha-emmission spectra from 15-MeV neutron bombardment of 54Fe and 56Fe in Figs. 31 and 32. In both cases the higher energy parts of the calcu- lated spectra agree reasonably with the data, indicating the applicability of the pickup and knockout corrections applied. The disagreement at the lower en- ergy portion of each spectrum [(n,na) contributions)] probably indicates the alpha-particle optical parameters are not completely suited to produce low- energy transmission coefficients. Since total charged-particle production cross sections are of interest to radiation damage calculations, theoretical curves for proton and alpha-particle production up to 40 MeV for 54Fe and 56Fe are shown in Fig. 33 along with available experimental data (see Refs. for Figs. 26-32). The arrows in Fig. 33 indicate thresholds for (n,pxn) and (n,axn) reactions.

F. Gamma-Ray Production Gamma-ray production spectra have been measured on natural iron for neutron energies between 1 and 20 MeV using both continuous and discrete energy neutron sources. Comparisons to such measurements allow us to test the general consis- tency of theoretical calculations since the data provide information pertaining to all reactions having significant cross sections at a given neutron energy. These data are further supplemented by cross-section information for the produc- tion of discrete gamma-ray lines. These data often represent some of the main information available at higher energies through which nuclear model calcula- tions can be verified. Figures 34 through 40 compare calculated spectra to measurements of Chapman et al.140 between 3.5 and 9.5 MeV. Good agreement exists except for portions of some calculated spectra that contain small contributions of discrete lines not seen in the data and parts of the continuum calculation between 5 and 8 MeV. The former problem results most likely from incorrect assignments in the gamma-ray branching information used in the calculation. The main discrete gamma-ray lines appearing in these spectra result from the 0.846- and 1.238-MeV . gamma-rays produced from inelastic scattering on 56Fe. Measured excitation functions141-153 for these 2 lines are compared to our theoretical results in . Figs. 41 and 42. ‘This comparison confirms not only the theoretical calcula- tion of gamma-ray cascades populating low-lying levels in 56Fe but also their population from’compound nucleus and direct-reaction processes. 39 i- 1 I I I I J n+54Fe--a +)( En=15MeV 1

~ IO-2 = \ n u u % u 10-3

I ‘1 t K)-41 I I I I I I I 3 5 7 9 II 13 Ea (MeV)

Fig. 31. Calculated and measured138 alpha emission spectra from 15-MeV neutron interactions with 54Fe.

n+56Fe+o+X En =15MeV

. I0-51 1 I I I I 1 3 5 7 9 II 13 Ea (MeV) .

Fig. 32. Calculated and measured138 alpha emission spectra from 15-MeV neutron interactions with 56Fe. 40 , 0 . a) e U)Q#- .

0w-l v . =

0N hi’

0

I 1 1,,1, , 1 I 1 t I 1 1 I 1 I 1 ,0 z 5 I 0 I (q)-

.

11 1 1 I 1 1 1 1,, ,,, 1 1 I It, ,,, 1 1 1 . 0 —. _ 0 6 0

41 EN = 3049–4.00MEV THETA = 125 DEG 0

+ CHAPMAN, 1976

M u-l- Ill-l%

+ 11”1 11111 111 I 14 1.1 J -1 ‘I ~+tu YI kl 2

‘iIL + ‘1 1+

,

I r I I I I I I ., I I I i 0.0, 0.5 1.0 1.5 2.0 Z.5 3.o 3.5 4.0 ENERGY (MEV)

Fig. 34. Calculated and measured 140 gamma-ray emission spectra from iron at 125 degrees for incident neutrons between 3.49 and 4.00 MeV. .

.

42 EN = 4.00–4.50MEV THETA = 125 DEG .

.

I + CHAPMAN, 1976

CL)y ‘o

0.0 1.0 2.0 3.0 4.0 5.0 6.0 io 8.0 GAMMA RAY ENERGy (METT)

Fig. 35. Calculated and measured140 gamma-ray emission spectra from iron . at 125 degrees for incident neutrons between 4.00 and 4.50 MeV.

. EN = 5.00–5.51MEV THETA = 125 DEG

F-

1 + CHAPMAN, 1976

s

C/2y “o l-l

1.

0.0 1.0 2.0 3.0 4.0 5.0 6.0 7.0 8.0 GAMMA RAY ENERGY (MEV)

Fig. 36. Calculated and measured140 gamma-raY emission sPectra ‘rem iron at 125 degrees for incident neutrons between 5.00 and 5.51 MeV. .

.

44 EN = 6.00–6.51NIEV THETA = 125 DEG

.

.

I ii + CHAPMAN, 1976

o

0.0 1.0 2.0 3.0 4.0 5.0 6.0 7.0 B.o GAMMA RAY ENERGY (IvIEV)

Fig. 37. Calculated and measured 140 gamma-ray emission spectra from iron at 125 degrees for incident neutrons between 6.00 and 6.51 MeV. .

. EN = ‘7.01-’7.51MEV THETA = 125 DEG

.

.

ti + CHAPMAN, 1976 \ my -o

n (72 1+J-l t-y ‘o

I l-l 0.0● 1.0 2.0 3.0 4.0 5.0 6.0 7.0 8.0 GAMMA RAy ENERGY (MEV)

Fig. 38. Calculated and measured140 gamma-ray emission spectra from iron at 125 degrees for incident neutrons between 7.01 and 7.51 MeV. .

.

46 EN = 8.02–8.52MEV THETA = 125 DEG

.

.

I t + CHAPMAN, 19’76

-’01 Iu!’111/~H CA l-y “- q,,,+, ,,+~,,~ ,,

, u [ 1 1 1 I I I I I I I I I I I 1 I + 0.0 1.0 2.0 3.0 4.0 5.0 6.0 7’.O 8.0 GAMMA RAY ENERG}7 (MEV)

Fig. 39. Calculated and measured 140 gamma-ray emission spectra from iron at 125 degrees for incident neutrons between 8.02 and 8.52 MeV. .

.

47 EN = 9.01–9.48MEV THETA = 125 DEG

I I 1 I I I i o 1

+ CHAPMAN, 19’76

o

., 0.0 12.0 G2fMMA4”kiY 8NERG8; (Id:)

Fig. 40. Calculated and measured140 gamma-ray emission spectra from iron at 125 degrees for incident neutrons between 9.01 and 9.48 MeV. .

.

48 FE(N,NGAMMA) EG=O.847MEV

t i

VAN PATTER, 1960 NISHIMURA, 1965 LA CHKAR, 1974 ORPHAN, 1975 BENJAMIN, 1966 BRODER, 197’0 DICKENS, 19’72 DRAKE, 1978 CLAYEUX, 1969 GRENI ER, 1973 SUKHANOV, 1970 ABEONDANNO, 1973 BRODER, 1966 + * I I I I I I I I I I I 1 I 1 1 I I I I I I I I ’10° 10’ NEUTRON ENERGY (MEV)

Fig. 41. Calculated (above 3 MeV) and measured excitation functions for production of the 0.847-MeV gamma ray from iron. The experimental data are from Refs. 141-153.

49 FE(N,NGAMMA) EG=l.238MEV

i .

o BRODER, 1970 N BENJA M IN,1966 ~ DICKENS, 1972 ~ LA CHKAR, 1974 E ORPHAN, 1975 + BRODER, 1966

I I I t I I I I I I 1 I I I I I I I I I )0 10’ NEUTRON ENERGY (M13V)

Fig. 42. Calculated and measured excitation functions for production of the 1.238-MeV gamma ray from iron. The experimental data are from Refs. 143-147, 153.

.

.

50 Further comparisons to the measured spectra of Chapman 140 for neutron en- ergies between 10 and 20 MeV appear in Figs. 43 through 49. Between 13 and 17 MeV there is a general deviation between our calculation and these data, which is somewhat surprising since the theoretical calculations of cross sections and secondary particle spectra around 14 MeV agreed well with several independent data sets. Furthermore, nuclear model calculations by Fu performed for ENDF/B- IV show similar departure in this energy range. Our results are in much better agreement with 14-MeV measurements made by Drake et al.148 as shown in Fig. 50. Between 17 and 20 MeV (Fig. 49), the calculations again agree generally well with the data of Chapman et al. The apparent underprediction of the dis- crete lines lying around 1-1.5 MeV in the theoretical gamma-ray spectrum results from use of spectrum bins to calculate (n,2ny) contributions (dominant for these secondary energies), which were much larger than the width of the bins used to report the experimental results. The 0.846- and 1.238-MeV gamma-ray lines as well as others from inelastic scattering were not affected by such a problem since in the evaluation their production cross sections are given separately (see Sec. IV E). Production cross sections have been measured144$154 for the 0.931-MeV gamma-ray produced in the 56Fe(n,2ny) reaction and are compared to our results in Fig. 51. The lower energy portion of the data of Corcalciuc et al.154 (circles) appear to be in error since they exhibit a threshold shape in an inci- dent energy region somewhat removed from the threshold for the (n,2nY) reac- tion. Our results do agree well with the data of Orphan et al.144 (squares) and with the higher energy portion of the Corcalciuc results.

G. Comparison of Higher Energy Proton Cross Section Data Since neutron reaction data are often sparse above neutron energies of 20 MeV, we compared calculated results for p + 56Fe reactions to experimental da- ta available up to incident proton energies of 40 MeV. Two checks were made from (p,p’) angular distribution measurements. Angular distributions measured . for levels excited by proton inelastic scattering were analyzed using DWBA cal- culations and the proton optical parameters of Table 11 to test the applicabili- . ty of these parameters at higher proton energies. Additionally, by making the assumption that the excitation of the collective levels in iron would be similar for inelastic neutron or proton scattering at higher energies, we checked the

51 EN = 10.0–11.0MEV THETA = 125 DEG

“o I I I I I I I [ I 0.0 2.0 . 12.0 GAMMA4;AY ::ERG? (ME:jO

Fig. 43s Calculated and measured140 gamma-ray emission spectra from iron at 125 degrees for incident neutrons between 10 and 11 MeV.

angular distribution predictions from our DWBA calculation, which employed the b neutron optical parameters of Table I. Further tests were made through calculations of 56Fe(p,xn) reactions us- ing the GNASH code. <hough the compound nuclei involved in the reaction chain for p + 56Fe reactions are different from those for n + 56Fe reactions, com- parison to such proton data does provide additional checks on proton and neutron - transmission coefficients, level-density parameters, and preequilibrium correc- tions. The agreement shown in Fig. 52 for calculated and measured55S155 (p,n) . and (p,2n) cross sections provides further confidence in the use of the parame- ters described in Sec. 11 at higher neutron energies.

52 EN = 11.0–12.0MEV THETA = 125 DEG

. 1 ‘– 1 I I

. +

+ CHAPMAN, 1976

w + l-l

h+

, u , , 1 I I I L 4 I I I i I I I 0.0 2.0 4.0 6.0 8.0 10.0 12.0 GAMMA RAY ENERGy (MEV)

Fig. 44. Calculated and measured 140 gamma-ray emission spectra from iron at 125 degrees for incident neutrons ● between 11 and 12 MeV.

53 EN = 12.0–13.0MEV THETA = 125 DEG

9 1 I I

+ CHAPMAN, 1976

w +-l SI

i I I I ~ I 1 I 1 1 I 0.0 2.0 4.0 6.0 8.0 10.0 12.0 GAMMA RAY ENERGy (MEv)

Fig. 45. Calculated and measured140 gamma-ray emission spectra from iron at 125 degrees for incident neutrons between 12 and 13 MeV.

.

54 EN = 13.0–14.0NIEV THETA = 125 DEG

. I

.

+ CHAPMAN, 1976

.,

0.0 2.0 4.0 6.0 “. 10.0 m GAMMA RAY ENERGY (MEV)

Fig. 46. Calculated and measured140 gamma-ray emission spectra from iron . at 125 degrees for incident neutrons between 13 and 14 MeV.

, EN = 14.0–15.1MEV THETA = 125 DEG o I I I

#

ii L + CHAPMAN, 1976

-L

h I I+4

(n ‘k t +

“o [ 1 1 1 0.0 2.0 4.0 6.0 8.0 1(’).0 12.0 GAMMA RAY ENERGY (MEV)

Fig. 47. Calculated and measured 140 gamms-ray emission spectra from iron at 125 degrees for incident neutrons beteen 14 and 15.1 MeV. .

.

56 EN = 15.1–1’7.6MEV THETA = 125 DEG

● ‘o 4* I I I I I

+ CHAPMAN, 1976

1

I I I 0.0 8.0 10.0 12.0 &MM:O RAYG”:NERGY (MEv)

Fig. 48. Calculated and measured 140 gamma-ray emission spectra from iron ● at 125 degrees for incident neutrons between 15;1 and 17.6 MeV.

.

57 EN = 1’7.6-20.1NIEV THETA = 125 DEG .

.

+ CHAPMAN, 1976

wcQ -F-- t rl + l-- I I

t

1I u 1 1 , I I I I I I ! - 0.0 6.0 8.0 10.0 12.0 &kmA4”Lw ENERGy (MEV)

Fig. 49. Calculated and measured140 gamma-ray emission spectra from iron at 125 degrees for incident neutrons between 17.6 and 20.1 MeV.

58 FE(N,XGAMMA) E = 14.2MEV 90 DEGREES

.

,

‘mo x DRAKE, 1975 \-l (n

I ‘o 1 I I I I 1 I I I A 0.0 1.0 2.0 3.0 4.0 5.0 6.0 7.0 8.0 !3.0 10.0 GAMMA ENERGY (MEV)

Fig. 50. Comparison of calculated gamma-ray emission spectrum at 90 degrees for 14.1-MeV incident neutrons with the measurement of Drake et al.148

59 I I I I I I I I I I I 0.2 56Fe(n,2ny) 55Fe =0.93IMeV ‘Y t I 0.15 n s w b 0.1—

0.0:

I I I I I I 1 I 10 12 14 16 18 20 22 En (MeV)

Fig. 51. Comparison of the calculated reduction cross section for the 0.931-MeV gamma ray from the ~6Fe(n ~n~)55Fe reaction with the measurements of Orphan et al. 14L (solid squares) and Cor~alciuc et al.154 (solid circles).

.

.

60 t I .

.

0,,1~ —

/ — / + — / —

I AO + — I + J(p,2n) 0.0 I— I

I I / 1 I I I I I I I 1 10 20 30 40 Ep(MeV)

Fig. 52. Comparison of the calculated (p,n) and (p,2n) cross sections for 56Fe with the measurements of Michel et al.155 (circles) and and Jenkins and Wain55 (triangles). Iv. EVALUATED DATA The calculated cross sections described here were integrated with the ex- isting ENDF/B-V file2 to produce a new iron evaluation extending up to 40 MeV. Significant changes were made in the ENDF/B-V data at energies down to 3 MeV. In this new evaluation we chose to rely almost completely on the calcu- lated results except for the total cross section. In particular, calculated values were used at all energies for reaction cross sections, angular distribu- tions, and energy spectra, subject only to a small (<10%) renormalization of the nonelastic cross sections above 30 MeV. We made this choice since in general the calculations agree well with most available types of experimental data, and the resulting neutron and gamma-ray production cross sections and spectra are consistent with each other. In this manner we avoid energy imbalance problems that affect some ENDF evaluations. For example, the present ENDF/B-V evaluation for natural iron violates conservation of total energy by about 9% around 13 MeV. We felt also that extensions of cross sections from energy regions having experimental data up to 40 MeV would be more reliable through use of nuclear- model calculations employing consistent parameter sets. Two evaluated data files were produced. The first contains dosimetry cross sections for neutrons incident on 54Fe and 56Fe. The second is a complete NAT ENDF/B evaluated data file for Fe, which includes cross sections, gamma-ray and neutron emission spectra, and their associated angular distributions. For the natural iron evaluation, we retained standard ENDF/B formats below 20 MeV to make this portion compatible with existing codes that use or process such data. Above 20 MeV, because of the necessity to include new reaction types not defined under present ENDF formats and in order to represent angular distributions asso- ciated with secondary neutron continuum energy distributions, we assigned new reaction type (MT) numbers and devised a method for representation of energy-angle correlated data. Details concerning methods used to represent the data both below and above 20 MeV as well as examples of evaluated cross sections and spectra are presented in the following sections.

A. Reaction Type Labels (MT Numbers) The ENDF/B reaction labels or MT numbers, either standard or newly defined, that were used for the dosimetry file are given in Table VI along with reaction thresholds. New reaction descriptors were required for the (n,2na), (n,3na),

62 (n,4n), (n,2np), and (n,3np) reactions, which are given respectively by MT=24, 25, 37, 41, and 42. Each dosimetry reaction is given over the entire energy range from threshold to 40 MeV. Table VII lists the reactions and thresholds used for the natural iron evaluation, together with the energy ranges of applicability. Above 20 MeV, a new MT=99 was defined to be the sum of the reaction types MT=16, 17, 22, 24, 25, 28, 37, 41, 42, and 91. This MT represents a composite of all major reactions resulting in the emission of continuum neutrons. (Inelastic scattering from discrete levels is therefore not included under this label.)

B. Representation of Neutron Emission and Associated Angular Distributions Below 20 MeV, neutron emission was described through a standard representa- tion involving discrete inelastic level information along with contributions from continuum inelastic scattering, (n,2n), (n,np + n,pn) and (n,na+ n,an) re- actions. Angular distributions for neutrons produced by inelastic scattering from discrete levels were generally a combination of results calculated from the use of compound nucleus and direct reaction theory. For those levels not as- sumed to be excited through direct inelastic scattering, only a compound nucleus angular distribution was assumed. Continuous energy secondary neutron spectra for a given reaction type were expressed in tabulated (histogram) form so that preequilibrium contributions, where applicable, could be represented adequate- ly. An angular distribution was assigned for each of these spectra based on its mean secondary energy though use of the Kalbach and Mann systematics72 for the angular distributions of continuum neutrons (see Sec. 11 E). Information con- cerning the foward peaking of higher energy neutrons was suppressed due to the averaging of neutrons of low and high secondary energies that is inherent with this representation. Above 20 MeV, angular distributions of secondary neutrons become much more forward peaked making it necessary to devise a method to represent such effects. As described in Sec. IV A, the use of MT numbers to represent individual reac- tions involving neutron emission was abandoned for the natural iron evaluation ● in favor of a new MT number, 99, which includes continuous neutron emission from all reactions present at a given energy. (The individual reaction cross sec-

✎ tions are preserved in the dosimetry files.) The composite neutron emission spectrum denoted by MT=99 was subdivided into 7 secondary energy groups each 5 MeV wide. To each of these groups a separate angular distribution was assigned, 63 TABLE VI

REACT~QNS, Q-VALUES, AND THRESHOLDS FOR THE 54F~ ~~d 56Fe DOSIMETltY FILES . 54Fe 56Fe — E E . MT (M:V) (M::) (M:V) (M:;) Reaction

16 -13.379 13.620 -11.197 11.399 (n,2n) 17 -24.062 24.497 -20.496 20.866 (n,3n) 22 - 8.418 8.570 - 7.614 7.751 (n,na) 24 -21.419 21.806 -19.653 20.008 (n,2na) 25 -32.001 32.579 -28.914 29.436 (n,3na) 28 - 8.853 9.013 -10.183 10.367 (n,np) 37 ------33.874 34.486 (n,4n) 41 -20.908 21.285 -20.410 20.779 (n,2np) 42 -31.443 32.011 -29.349 29.879 (n,3np) 103 0.085 EXO - 2.913 2.966 (n,p) 107 0.843 EXO 0.326 EXO (n,a)

TABLE VII

REACTIONS, Q-VALUES, AND ENERGY RiNGES INCLUDED IN NATURAL IRON EVALUATION E Energy Rection MT (M:V) (M::) Range (MeV) Description

1 7.646 EXO lo- 11-40 Total 2 0. EXO lo-~l_40 Elastic 3 7.646 EXO lo- 1l_40 Nonelastic 4 - 0.847 0.862 0.862-20 Inelastic 16 -11.197 11.399 11.399-20 (n,2n) 22 - 7.614 7.751 7.751-20 (n,na) 28 - 8.853 9.013 9.013-20 (n,np) 51-90 - 0.847 0.862 0.862-40 (n,n’) discrete 91 - 4.878 4.966 4.966-20 (n,n’) continuum 99 -19.645 20.000 20-40 Sun of MT=16,17,22 24,25,28,37,41, 42,91 102 7.646 EXO lo- 11-40 (n$Y) ‘ -1 l_40 . 103 0.085 EXO 10 (n,p) . 104 - 7.959 8.102 8.102-40 (n,d) 105 -11.928 12.144 12.144-40 (n,!) . 106 -10.533 10.723 10.723-40 (n, He) 107 0.326 EXO 10- 1l_40 (n,a)

64 again through use of the Kalbach systematic. In this manner, angular distribu- tion effects were introduced for continuum neutrons and, along with discrete level angular distributions obtained through DWBA calculations, a reasonable representation was obtained for the physical processes occurring at higher inci- dent energies. This method has some disadvantages as will be noted later, but for this evaluation it represents a first step towards ENDF formats that will describe energy-angle correlations.

c. Neutron Cross Sections The evaluated cross sections for the reaction types listed in Table VI were determined purely from the theoretical results as described earlier. In this section we present cross-section curves only for reaction types not already com- pared to experimental data in Sec. III. Further detail regarding some of these cross sections appears in Appendix B , which tabulates the dosimetry cross sec- tions calculated for individual reactions with 54Fe and 56Fe. 1. Total, Elastic, and Nonelastic Cross Sections. The evaluated total cross section for natural iron is compared to experimental measurements6-19 and to ENDF/B-V2 in Fig. 53. The total consists of ENDF/B-V values below 10 MeV and then follows the recent measurements of Larson 13 to 40 MeV. These da- ta were chosen since they cover the widest range of incident energies and agree well with the previous measurements of Perey, 6 which cover a similar although somewhat smaller energy range. The evaluated elastic cross section is shown with experimental data (Refs. 22-24,26,32,47,87) and ENDF/B-V in Fig. 54. The evaluated elastic was joined to the ENDF/B-V values at 8 MeV. Between 8 and 40 MeV, it was determined from the difference between the evaluated total and the sum of the various components of the reaction cross section. The nonelastic cross section used in the evaluation is compared to experimental data37-50 and to ENDF/B-V in Fig. 55. The nonelastic cross section was generally derived from values calculated with the optical parameters of Table I except in the region around 30-40 MeV where these values were renormalized downward by a maximum of 10% to agree with the recent results of Brady et al.,37 which were not available for use in the determination of the optical parameters.

65 FE TOTAL CROSS SECTION

3xld’ 10’

❑ BRADY. 1979 0 DECONNINCK, 1961 0 PETERSON, 1960 K ROBINSON, 1!309 v A NGELI.1970 x MC CALLUM; 1900 A PEREY, 19’72 @ FOSTER, 1967 + CIERJACKS, 1970 ❑ LARSON, 1979

1 I 1 I I _l I 1 I 8*ld’ 10’ NEuTRoN ENERGY (MEV)

Fig. 53. Evaluated and measured total cross section for iron. The dashed curve is ENDF/B-V, the solid curve is the present evaluation, and the experimental data are from Refs. 6-19.

66 FEELASTIC CROSS SECTION

~ WILENZICK, 1965 Ii a HOLMQVIST, 1969 ‘1 0 KINNEY, 1970 1!1 I K MACHWE, ----1~~~ +GILBOY, 1965: 1’1111. 1 v Hf)~MQV]ST,: 197(

., $.,, * ,“ t’

COON. 1958 I K1NNi3Y,1970 HOLMQVIST, 1970 1

q o I I 1 I 1 1 I 1 1 I 8“ld 10’ NEuTRoN ENERGY (MEV)

Fig. 54. Evaluated and measured elastic cross section for iron. Experi- mental data are from Refs. 22-24, 26, 32, 47, 87. See caption of Fig. 53 for curves.

67 FE NONELASTIC CROSS SECTION m < 1 8 1 1 I B 1 s . q ,.-----...... ------...... z“ 0 Q . :s .. t —: la + mm ,’ ❑ WALT, 1955 ❑ BEYSTER, 1955 0 N MACHWE, 1959 ~o v TAYLOR, 1955 u“ o PASECHN1 K, 1955 + BEYSTER, 1956 q o I !1 1I 8t 1I 1 I1 !I I 3=100 10’

N0 1 I [ 1 BRADY, 1979 MAC GREGOR, 1958 I

8*ld’10’ NEUTRON ENERGY (MEV)

Fig. 55. Evaluated and measured nonelastic cross section for iron. Experimental data are from Refs. 37-50. See caption of Fig. 53 for curves.

.

. 2. Inelastic Cross Sections. Discrete inelastic cross sections for the lowest 33 levels in 56Fe and the lowest 7 levels*in 54Fe are included from threshold to 40 MeV in the evaluation. Continuum inelastic scattering (Eth = 5 MeV) is tabulated in MT=91 below 20 MeV and is combined in MT=99 above 20 MeV with all other neutron-emitting reactions except discrete (n,n’). Comparisons of the calculated and measured excitation cross sections for low-lying levels of 54Fe and 56Fe were presented in Figs. 13-19 of Sec. 111. B. Figures 56-58 compare the ‘ATFe excitation functions for the first 10 levels included in the evaluation with ENDF/B-V values in cases where the latter exist for the same states. These levels include the low-lying collective states of these nuclei that have a significant cross section up to 40 MeV be- cause of calculated direct reaction components. These cross sections as well as the remainder of the discrete level inelastic cross sections (MT=61-90) were joined to the ENDF/B-V results near 3 MeV. The total inelastic cross section (MT=4) is compared to available experim- ental data86S 137S146Y156-161 and to ENDF/B-V from 2 to 20 MeV in Fig. 59. The very old measurement of Landon160 (1958) near 14 MeV disagrees with both ENDF/B-V and the present evaluation. 3. Fe(n,y) Cross Section. The (n,y) cross section is represented expli- citly under MT=102 at all energies to 40 MeV. Statistical theory GNASH calcula- tions were coupled with a preequilibrium-like semi-direct calculation above 3 YeV to obtain the evaluated curve. ‘L’heresults are compared to ENDF/B-V and to the available experimental data162-164 in Fig. 60. 4. Fe(n,2n) Cross Section. The (n,2n) cross section is represented under MT=16 below 20 MeV and is included in MT=99 at higher energies. The results for 54Fe and ‘ATFe were compared to experimental data in Figs. 24 and 25 of Sec. 111 c. The results for ‘ATFe are compared to ENDF/B-V and to additional experi- mental data165~166 in Fig. 61. 5. The Fe(n,p) and Fe(n,a) Cross Sections. The evaluated (n,p) and (n,a) cross sections for natural iron are given explicitly under MT=103 and 107 from 10-5 ev to 40 MeV. Comparisons of the present results with ENDF/B-V are a included in Fig. 62. Comparisons of the constituent isotopic results to experiment were presented earlier in Figs. 26-33 of Sees. 111 D and E. .

*The J= = 6+ fourth excited state of 54Fe at Ex = 2.9501 MeV was omitted due to its small cross section.

69 n EX=O.847MEV MT=51

.

.

EX=l.408MEV MT=52 z z ! I I I 1 1 1 1 I I 1 3 ZN g ‘a g+ ------...... _ ------w v+ ~o rg* E ~y

EX=2.085MEV MT=53 Gw- ‘0 z“ 0 qY ~o . ;+ m g ‘~ o a U? ! t I I 1 I 1 { 1 t ! o 1 I I 1 1 1 I I ! I ’10° 1 NEUTRON ENERG;O(MEV)

. Fig. 56. Evaluated Fe(n,n’) cross sections for the first three discrete states. The solid curve is the present evaluation and the dashed curve is ENDF/B-V.

70 EX=2.658MEV MT=56 E . JO 04 . ~ ~lx.10 CA- Cf2 2 q

o 1 1 ! 1 ! I 1 I 1 f I 1 1 1 # I 1 1 1 I 1 1

EX=2.960MEV MT=59 n Iu q ~ z o ~& Ga VI V-J. o“ u q

~ 1 1 1 J 1 1 1 1 1 I [ 1 I 1 1 8 II i 1 10° 10’ NEuTRoN ENERGy (MEV)

. Fig. 57 Evaluated Fe(n,n’) cross sections for the 6th, 7th, and 9th discrete states. See caption of Fig. 56 for curves. .

71 ‘o“$ +++++

+ \ +* + MT=53+++ L ++ +++++++ ‘%

t I I [ I I ! ! ! 1 I 1 I I 1 I 1 1 I I ENERG;O~MEV)

Fig. 58. Evaluated Fe(n,n’) cross sections for the 4th, 5th, 8th, and 10th discrete states. The dashed curve is ENDF/B-V; the solid curves, triangles, and crosses are the present evaluation. .

.

72 FE INELASTIC CROSS SECTION

la -o 0 +

e JOENSSON, 1969 B BEGHIAN, 1955 ‘! ❑ BARROWS, 1965 ❑ THOMSON, 1963 ‘. v PROKOPESC, 1969 ‘. o LA NDON, 1958 \ ‘. x JACQUOT, 1966 + BRODER, 1970 o HOPK INS,1964 ‘o + * I I I 1 1 [ 1 I t 1 1 I 1 1 n)‘“~.looI I 10’ NEUTRON ENERGY (MEV)

Figs 59. The inelastic cross section of iron from 2 to 20 MeV. The solid curve is the present evaluation; the dashed curve is ENDF/B-V; and the experimental data are from Refs. 86, 137, 146, 156-161.

6. The Fe(n,np) and Fe(n,na) Cross Sections. The evaluated (n,np) and (n,na) cross sections for natural iron are given to 20 MeV under MT=28 and 22, respectively. These results are compared to ENDl?/B-V in Fig. 63. At higher en- ergies, contributions from these reactions are included in the MT=99 composite for ‘ATl?ebut are tabulated individually in the 54Fe and 56Fe dosimetry file. . 7. Fe(n,d), Fe(n,t), and Fe(n,3He) Cross Sections. The evaluated cross sections for the (n,d), (n,t), and (n,3He) reactions are shown in Fig. 64. We . did not attempt to calculate these with theoretical models since their cross sections are small and the parameters and reaction mechanisms associated with them are somewhat uncertain. For the (n,d) reaction, we assumed a shape similar 73 FE(N,GAMMA) CROSS SECTION

m ~ ‘o n--- 0+=$ y-- ...... L ...... __.. /~”- ] a

\ x CV ELBAR, 1969 -1- — y A DIVEN, 1960 o + MALYSHEV, 1964

(f! I I I 1 I I I I I I o I 1 I 1 I 1 I 1 I “L-’10° 101 NEuTRohJ ENERGY (MEV)

Fi . 60. Evaluated and measured162-16 ~ cross section for the Fe(n,Y) reaction. See caption to Fig. 59 for curves.

to that for the (n,p) cross section (adjusted for threshold differences) and normalized the curve to the integrated deuteron emission spectrum measured by Grimes et al.138 at 14 MeV , since at this energy the (n,d) reaction domi- nates. A similar approach was followed for the (n,t) reaction with the normali- zation determined from the 14-MeV systematic of (n,t) reactions as described by Qaim.167 For the (n,3He) reactions the cross section was assumed to have a shape similar to that for the (n,a) reaction (again adjusted for threshold dif- ferences), and the Qaim (n,3He) systematic were used for absolute normaliza- tion at 14 MeV. The present results for the (n,d), (njt) and (n,3He) cross sections are seen in Fig. 64 to be significantly lower than ENDF/B-V.

74 FE(N,2N)CROSS SECTION

...... ------.----- ,. ..” / i ------. . \ ,.------. ., ,,, ?’ ,, .’ ,’ .’ .’ , j ,’ .’

,’ .’ .’ ,’ ,’

x WENUSCH, 1962 ~ V EESER,1979 + ASHBY, 1958

.,” .. I I I I I 1 I I I I 1 I 11.0 12.0 13.0 14.0 15.0 16.0 17.0 18.0 19.0 ).0 NEUTRON ENERGY (MEV)

Figs 61. Evaluated and measured97S165’166 cross section for the Fe(n,2n) reaction. See caption to Fig. 59 for curves.

Il. Neutron Emission Spectra Comparisons to experimental spectra measured for 14-MeV neutrons shown in Sec. III B indicate that the calculated spectra provide a realistic representa- tion of this data. Here we show examples of neutron emission spectra calculated

● at higher incident energies to illustrate angular distribution effects that are present as well as the need to incorporate them into the evaluated data file. , Figure 65 shows the laboratory angle dependence of the secondary neutron spectra induced by 36-MeV neutrons. The higher energy portions of the spectra contain discrete level cross sections (elastic and inelastic) that exhibit a large 75 FE(N,ALPHA) CROSS SECTION 1 1 1 r 1Ii ..... , , , 1

y ~. -

‘? o– .

7 7 , I I I , , 1 I , ! , 1 I t I I 1 , I I ~ [ / 0 :; , I I 1 1 1 I 1 I t , 1 1 1 I , 1 I I 1 10° ‘3*ld’ 1ni NEUTRON ENER& (MEV) NEUTRO~-ENERGY (MEV)

Fig- 62. Evaluated (n$p) and (n,a) cross sections for iron. Curves are the same as described for Fig. 59.

degree of forward peaking. Likewise, the continuum energy region between 10 and 25 MeV exhibits a similar dependence with almost a factor of ten difference in cross section between forward and backward angles. The discontinuity.es shown are artificial and arise from the assignment of one angular distribution to each 5-MeV wide group of secondary energies. ‘l’hisproblem indicates that a format should be de!rised that would allow angular distributions to be assigned for smaller secondary energy ranges in a compact manner. Such an effort is in progress.

E. Gamma-Ray Cross Sections and Spectra . Discrete gamma-ray lines from inelastic scattering are included in the evaluation from threshold to 40 MeV. The discrete data are given as multiplici- . ties in ENOF/B File 12 and are assumed to have isotropic angular distributions. Gamma lines from all other reactions were binned with the continuum gamma rays

76 FE(N,NP)CROSS SECTION FE(N,NALPHA) CROSS SECTION 7 0 I , # ,. ,...,”’ ,., ZT ,..’ =o- - ... .-1-- #.. z 0 ,.$ G u 7 w 0- - m .+ -- m m gy

‘i’ 0 -- ‘? .-l I I t 0 , , [ *m , I 1 I 8*ld’ ‘ “ 8*& ‘1 N&TRoN ENERGy (MEV) N&TRON ENERGY (MEv)

Fig. 63. Evaluated (n,np) and (n,na) cross sections for iron. The curves are described in the caption to Fig. 59.

and are represented as tabulations in Files 13 and 15. Again, isotropy is as- sumed in all cases. As with the neutron files, gamma rays resulting from all reactions that produce neutrons (except discrete inelastic) were lumped under MT=99 for incident neutron energies above 20 MeV. A large portion of the gamma-ray production spectra has been compared in Sec. III F to experimental data available up to neutron energies of 20 MeV. We show here in Fig. 66 examples of gamma-ray production spectra calculated for higher incident neutron energies (28 and 40 MeV). These spectra illustrate the increasing importance of continuum gamma-ray contributions with a decreased con- tribution from discrete lines. However, the 0.846- and 1.238-MeV gamma rays . from 56Fe(n,n’) and the 0.953-MeV gamma ray from 56Fe(n,2n) are still iden-

. tifiable at these higher energies. The total calculated gamma-production cross section maintains an almost constant value of about 2 barns in the neutron ener- gy range between 20 and 40 MeV.

77 FE(N,D)CROSS SECTION FE(N,T)CROSS SECTION , ,...... $’ ... 0 EiI ... -o ,.. zo ~ ; ‘? o u) CIN U-Jo C&” CJ“;;(T; 7 0

7 0 I , I f , ‘8”ld’10’ 10’ NEUTRON ENERGY (MEV) NEUTRON ENERGY (MEV)

10’ NEUTRON ENERGY (MEV)

Fig. 64. Evaluated (n,d), (n,t), and (n,3He) cross sections for iron. The curves are described in the caption to Fig. 59.

.

78 .

90°

.

I I ! I 00 1 0.0 N::TRON E%’RGY (ht%)

Q-

00

A 3 $ -y z o. 0-; ~ m g~- - g

To - 0.0 10,0 20.0 1.0 NEUTRON ENERGY (M%)

Fig- 65. Calculated neutron emission spectra at O, 90, and 180 degrees for 36-MeV neutrons incident on iron.

a

.

79 .

.

40 MEW

?.0 GAh4h4A RAy ENERGY (MEV)

Figs 66. Calculated gamma-ray emission spectra at 90 degrees for 28- and 40-MeV neutrons incident on iron. .

. v. suMMARY A consistent set of nuclear models and parameters for calculating neutron- induced reactions on 54Fe and 56Fe between 3 and 40 MeV has been presented. The calculations were made using a multistep Hauser-Feshbach statistical model with corrections for preequilibrium and direct-reaction effects. A spherical optical model was used to determine neutron, proton, and alpha transmission co- efficients, and gamma-ray strengths were parameterized to calculate photon emis- sion. Extensive comparisons with experimental data, including neutron-, proton-, and alpha-induced reactions, show that the calculations are in general agreement with most of the available experimental data. The calculated data were used to develop two ENDF/B-formatted evaluated da- ta files: a dosimetry file , which includes individual 54Fe and 56Fe neutron- induced reaction cross sections to 40 MeV; and a complete, general purpose ‘ATFe file, which was joined at lower energies to ENDF/B-V and which includes neutron- and photon-production cross sections, angular distributions, and energy spectra from 10-5 eV to 40 MeV. To describe the data above 20 MeV, new formats, proce- dures, and reaction type ‘“labels’”were developed for the ENDF representation, and some lumping of reactions was found desirable for the natural Fe evalua- tion. Both evaluated data files have been provided to the ENDF/A library in the National Nuclear Data Center at Brookhaven National Laboratory. The use of nuclear theory to augment the rather sparse experimental data base above 20 MeV has been suggested16g as the most feasible way to extend eval- uated data files to the 40-50 MeV regime in the detail needed for certain appli- cations. The present work verifies that such extensions are indeed feasible and can lead to internally consistent evaluations that are in good overall agreement with experimental results.

81 I

APPENDIX A

DISCRETE LEVELS USED IN THE CALCULATIONS

. ~1- =&& . 24048 0.0000 0.0 + 24052 0.0000 7g7s4 2.0 + 1.4342 4.0 + 2.3698 3:4200 :: : 2.6470 3.4520 . 2.7680 2.9650 24049 0.000o 3.1138 0.2720 t; : 3.1620 1.08S0 4.5 - 3.4153 lJSGZO S.c - 3.6166 1.7040 1.5 - 3.7710 1.7420 3.9510 1.9820 ::: + 4.0154 2.1690 1.5 - 4.0400 2.4330 4.5630 24980 k: : 24053 :Oo& 24050 0.0000 0.0 + 0.7833 2.0+ 1:0060 1.8814 4.0+ 1.2895 2.9250 2.0 + 1.5365 3.lell 2.0 + 1.s736 3.1637 6.0 + 2.1724 3.3246 4.0 + 2.2332 3.5945 3.0 + 23205 3.6110 :: : 2.4530 yg 2.6570 0:0 + 26700 3:6980 2.0 + 3.7920 5.0 + 24055 0.000o 3.8254 6.0 + 0.2440 0.5210 24051 0.000o 3.s - 0.5720 0.7490 o.8mo 0.7770 2: : 1.1645 4.s - 2s0s 1 0.0000 1.3500 2.s - 1.4803 :: - 1.5574 .- 1.8994 2.0010 ;: : 1.8246 2.2557 7.5 - 1.9589 2.3130 2.1403 2.3796 u : 2.2559 2.38S6 6.5 - 2.2759

82 Levo I&orgy 5pIn Lov. ~c~rgy 5pln NUCIOU9 !W!!Y Nuc t● US &!!Y

25052 0.000o 6.0 + 25055 ::) 0.3778 2.0 + k:: 0.5459 1.0 + $;::; 4.5 - 0.73 1s 4.0 + 5.5 - 0.82s2 3.0 + 1:5298 1.5 - 0.8697 7.0 + MiE U : 3.s - “ 22153 2.5- y: - Z2525 .- 2L2690 ::: : p;: Z3118 ;:: ~ 23660 E : $::;;: .- 25056 0.0000 3.0 + 2k30 :::: 0.0266 20 + $:;:: 0.1105 1.0 + ;! : 0.2120 :: : 2:6870 0.2150 2.6935 7.5 : 0.3355 5:0 + 2.6973 M - 0.3410 3.0 + 2.7070 0.5 + 0.4540 4.0 + 0.4860 3.0 + 25054 0.0000 3.0 + 0.7160 3.0 + 0.0545 2.0+ 0.7540 3.0 + 0.1562 ~: : $43:: 3.0 + 0.3680 1.0 + 0.4078 3:0+ 1:1660 1.0 + (p; 4.0+ 3.0 + 25057 0.000o 2.5 - ;::;:; 6.0 + 5.0 + 25058 0.0000 3.0 + ;::&4g :: : 26051 0.000o 2.5 - 1:4S42 <0 + 0.2700 3.5 - 1.S085 3.0 + 1.5437 3.0 + 26052 0.0000 0.0 + 1.6340 :: : 0.;::: 2.0 + 1.6508 4.0 + 1.7840 7:0 + 2.7400 2.0 + 3.5500 2.0 + 3.5900 4.0 +

83 L.v. llfmrgy Spin L.v.~~~rgy Spin Nuclws Parlt y Nucl Olm Parity

26053 26056 0.0000 0.0 + :Eo 0.8468 20 + 1.3280 %08s 1 4.0 + 1.4240 2.6576 2.0 + 1.6970 2.9417 0.0 + 20430 2.%00 Zo + 23390 3.1200 1.0+ 3.1230 4.0 + 26054 0.0000 3.3702 ~: : 1.4084 3.3880 205384 3.4450 :.; : 25613 ::= 2.9500 2:0 + 2.9590 3:6070 0.0 + 3.1661 3.7556 6.0 + 3.2952 ::M2: 20 + 3.3450 3.0 + 3.8340 4:0490 3.0 + 4.0280 4.1003 3.0 + 4.0400 4.1200 4.0 + ::;&o 4.2960 4.0 + :;:: 0.0 + 4:2920 3.0 + 4.5790 4:4010 2.0 + 4.4580 3.0 + 260s5 O.0000 4.5100 3.0 - 0.4115 4.5395 1.0+ 0.9313 ~::;: 3.0+ 1.3167 2.0 + 1.4066 4:6600 3.0+ 1.9190 4.6847 3.0+ %0s20 4.7299 0.0+ Z 1442 4.7396 2.0 + 202119 4.8780 20 + 2.3009 Z4700 26057 0.0000 0.5 - 2.5390 0.0144 2.5779 0.1365 # : ~m: 0.3667 :$:;; 2:5 ~ 2:9390 3.5 - 2.9830 1:1980 29840 1.2650 ~: ~:;;: 1.3657 1.6277 ;::- 3:1090 1.7257 1.9750 0:s : 1.9894 4.5 - 2.1170 2.5 - $::;: +; -

2:3350 0:5: 2.3550 5.s - 2.4550 4.5 + 2.5060 2.5 +

84 APPENDIX B

LISTING OF THE 54Fe AND 56Fe DOSIMETRY FILES IN ENDF/B FORMAT (See Table VI in the text for definition of the MT numbers) .

i?;bO$dE+OU S,5ib5E+nl 0 0 Fi265uli! 16 0 0. ●lm3379E+e7 0 0 : 3S2bSul@ lb lb : 16 3 16 4 l;6000E+07 3,7300E~U2 1.b5~C~E+0t U9752UF-tli? 1.71!FI@E+a7 5;6BflJE-P2?65410 lb 5 lp7S00E+07 60461aE=02 1.80~~E+07 7.!3ak~E-@2 1:85UOE+I?7 7,b~flHE-?i?2b5u10 16 b l,9000E+f17 8.fA9@~lE-@a l,95@qE+fAT PmU65FjE-t?Z 2.:IAi31aE+@7 8,75i3tiE-@2Zb~ul@ lb 7 2p1090E+07 9,1030E-OZ 2.ZC10k3E+0? 9.4@0@E-a2 2p3nO~E+@l 9,b78tiE-022b3410 16 8 ZpUI?0@E+07 9,8fItJ0E=02 2a5FifleE+07 9,71i?0Eoai! 2$bt?Gl@E+f47 9,3UtiQEw022b3u10 lb 9 2.7000E+ti7 8.7U1OF-O2 2.8naflE+07 R.1UO14EWC4Z 2mQv\:@E+@7 7,5b7Qk-0~?b5fJl@ lb !0 3q0000E+d7 b,Q548E-(72 3.1(30$7E+1J7 f)a3hb2F-C12 3.2ni3LJE+G17 5,8eb2E-f12?b5fJlfi lb 11 3p3009E+07 5,42$3QE-Q2 3.ucA~’PE+G7 5at31uuF-f12 305aoflE+07 fl.63b~t-022b5ul@ lb 12 3pb000E+07 u.2963t-92 3.703~E+k~7 Ua~lU?F-OZ 3.8flL!QE+@7 3,7~91E-U22b5uld lb 13 3.9000Et07 3,5403E-@2 4.00tiL3E+07 3.3U39E-QZ 26s410 lb lU i?b!i41n 15 2;605dE+@a 5,S3b5E+0j a 0 0265410 1; 0 0. 02,0062E+07 a : 172bSfJ10 17 5 2 1! 5“ 2b541t3 17 ; 2;U49fE+07 0, 2.500dE+@7 lmU359Emt34 2gb0tJ0E+fj~ U,2Q0bE-f182bS41@ 17 3 2P7@00E+07 7,14S3E_04 I?.nOO@E+Of 1,00~0E-03 Zp90k10E+Q? l,5566E=03?65u10 17 4 SpOOO@E+O? z,24Q13EQ93 3.l@tiOE+~T 3.0242E~03 3,2000E+07 3.8@9ZE-a326S410 17 s 3,300BE+c37 u,fi560E-03 3.fJI?00E+07 5.2408E-a3 3P5019W+37 5,8390E*0326541fl 17 b 3,6@00E+07 b.S0a9E-03 3.700t?E+E17 b06957E~03 3.801?OE+0? b.Qb79E-kY3Zb!541ti 7 3.9@00E+07 7,1728E-03 4.0000E+07 7.214BE-03 i!b5Ql@ :; 8 2b~41Q 9 2;b8sQE+0u s,S31)5E+0\ 0 0 02b5ulfi 2: 0 0. -8,Ut80E+06 e : 53265410 22 15 z : 2654!0 22 : 8;5T0@E+i3b 0, 8,b00iiiE+;: f,$309E=97 8;7W30Et0h 9,1852E-0726~410 2i? 3 8,8Ci00E+@6 1,$737E-66 9.tiFi~OE+06 2.19Q2E-t36 9~i?QW?C3E+a6 3m21U8E~flh2b5ul@ 22 4 9p25BflE+0b 3,h700E006 9,4000E+06 U0235UE-06 9p530t?E?@b &m7U57f-062b9u~Q 22 5 9,6000E+06 5.2560E-t3fa 9.750fiE+f16 6.0214E-@6 9.80c30E+r36 b,2765E-0b265uld b l,@B00E+i37 7,2V71E-ab la0500E+07 9.hUf3bE~Ob l.l~O@E+a$ 1.2U0i3E-@52bS410 :: 7 tp\S00E+07 5,93fF10E-@S lmF?0t3BE+D7 beb8f113E-05 l,250f4E+a7 7.4u0UE-@sZb5u!8 2i! 8 lp3000E+07 l,0003E-flu 1.350tIE+f47 t?.Q400E404 1.U000E+k37 7,@5fl@E-f142b5ul@ 22 9 l,450flE+07 1,395aE-a3 lm5fl@t3E+O$ 2c3300Ew03 1.550GiE+d? 3,8550E-032b5ul!iI 22 la lp6000E+07 6,2800E-Iz13 lsb50@E+97 1.0160E-02 1.7’20@E+@7 l,620~E=922b5410 22 11 l,7!100E+07 2,3136uE-F12 l,80nOE+D7 3.t?ZOOE-OZ 1.8500E+B? 4,1U0@E=0aZ65410 22 12 1.9000E+07 5.cIVfl~E-C12 1.95Q0E+07 3m9790E-02 2ptitI?80E+P7 6,8k~BtiE-a22b5ftifl 22 13 2pla00E+07 8,td70E-fd2 2.20GflE+t37 9m$20tiE-02 2.3i?kJQk+tJ7 1.O14QE*O1265U1O 22 lU 2,UfJ00E+07 l,9700E-01 2.50UfIE+07 lm135tiE-al 2.tIonnE+t)7 l,178@E-P12b5410 22 15 Z,7000E+07 l,1300E=01 2a800@E+07 9.b000E~FJ2 2.9t380E+07 7.47UOE-02269410 22 3p000BE+f17 5,6693E-a2 3.l@fJnE+07 4.R954E-02 3.2qnnE+ti7 3,3331E*02t?b5410 22 :! 3pS000E+07 2.6445E-aa 3.4cIt3!E+Q7 ~a1091E-02 3.5nflaE+0t l,b87bE-Q2265u10 22 18 3,b000E+07 1,BS11E=02 3.7t3QmE+U7 1.0813Ew02 3.8800E+07 8.57i31E*03Zb5fIlU22 3.9000E+07 6,8S08ED03 4.0009E+0? 9,4317E*03 Z65LJ10 22 K a 2bS4i0 n 21 2~60ShE+$U 5.5Sb5E+fl”l e a 0265410 a 0. ●2,!419E+Gi7 1 20265410 :: . 2 2: : i?65410 24 : 2;18a6E+0~ 0, “ 2ei?f10dE+b37 R,8423E

86 3p70QJ0E+06 2,3W1Z’EWO1 30060@E+06 2mU660E-121 3,90B@f+@b 2.6328E-012b54 3103 il.08%0E+06 2,df100E=01 4,1000E+06 2,9691E.Q1 u,2@0@E+tj6 3,1373E-01~6siJ 31(33 : 4;3flQl@E+Gjb 3,3@3uFm@t 4,4@fJoF+(lb >mU664F-fll 4m50C41?E+@6 3,6251E-a1265u 31k13 7 ilp60@tIE+a6 3,778SE-a\ 4.7@H@E+@b 3.9256Eo01 4,8rnOflE+k~6 4.13b54L-@Ii?654 3103 8 4p9000E+0b 4,1Q72E-cI1 5.0uO13E+@6 Uo~2tW-L31 5.200VE+Lf6 4,5307E-0i265U 31B3 9 ● 5p2s0flE+@b 4,9?58Ewfil 5.u0@GIE+@6 4,6939Fw01 5,5~fiflE+Q6 U,75~’lc-@12b54 3!93 lfl 5p60013E+06 4,@154E-@l 5.75~@E+06 4.6832E-tJl S.80@@E+@6 4,9f~.2?E-012bS4 31G43 11 6.00@0E+06 4.Q6~I~E-@l 6,2@~OE+L46 5m005vE-Gl 6025@@~+k16 5,’3158E-012654 3103 12 * 6p4000E+0b 5.PU5f3E-C!l 6.5nOOE+k?6 5m0b3UE-@l b.6’3k!@t+f)6 5,0787E_01Pb!34 3103 13 6,75a@E+Vb 5.0965E-121 b.8nfiPE+Uh 5.10a9EwOl 7.f5flf13E+r16 5,11flflE*@12b543tk?3 14 7p2000E+61b 5.ll16E=fil 7.25kIOE+~6 5.lli(lE-01 7.U00VE+ti6 5,112VEW312654 3103 15 7p5000E+0b 5,11tSE-@l 7,6n08E+@6 5,11135Ewai 7.7S00E+06 5,1G79E-L31Zb9U 31f13 16 7p800@E+Ob 5,1nb7E-01 8,f40@~F+06 5,1@@@E-01 8DZf18@E+@6 5,G~16E-91?b54 3103 17 8.25@BE+~6 5,0894E-P1 8.uFkl@E+P6 5.~822F~@l 8p5~@flE+L’6 5.k’7hQE~312654 31k13 la 8p6000E+06 5.@71@E-al 8.75@fiE+~6 5.06a9F*@l B.89~?fiE+~6 5.9572E-01i?65U 31,15 19 9,0000E+06 5,fd4RflE-01 9.2(IOOF+06 5mC1173EW91 9.z5r?OE+@6 5,RlP~E*~12b54 3103 2a 9pQ00@E+0b u,9898E-nl 9.5flQ’ZIE+klb /Jc9753E~91 9.6C10fflE+kj6 Uo9e@9E-F112b54 31@3 21 9p800@E+Ob 4,9334E-EI1 l.@OOflE~~? Um91nPEW91 l.O!!itiPE+@t 4,87?1L-012’654 31C3 22 lp10fi0E+97 U,~U0f3E-G?l 1,15S3E+07 4.7738E-(11 IP22(IC?E+27 4,6F9L’EvQll?6g4 31d3 23 l,2500E+07 4s3199E-61 1.3f10f?E+07 u.25~0E~Ql 1.3500E+U? 3,8761E-@12654 3103 24 l,Q000E+07 3,f+90LlE-01 l,4509E+07 30C4407EW01 1.5C38CEt0? 2.6500E-0126S4 3103 25 l,550BE+@7 2,26)3tiE-01 1.600t3E+0t 1.95f10E*@l ;p6500E+W7 l,bu75E-0i2bS4 3103 26 l,7000E+07 le~R@[email protected]~flE+~71.2080E_01 lp8f10@E+f17l,@5kI~E-@126!J41elQ3 33 l,6S00E+97 9,193QE-02 1.90kI@E+Id78,129EE-Q2 l,9500E+07 7.2b6@E?@22b5u’0103 34 ZpO@O@E*@? 6,$80@E=Q2 2.l~fl$?E+~75,50n0E=02 2~2f10@E+u74,69fl~E~V2E6SU’01(33 35 2,3000E+07 4,ab~~E-OZ 2.4000E+a? 3.61OOE-Q2 2.5000E+@7 3,271OE-Q22654’ 0183 36 Z~60BBE+07 .2.91QaE-02 2m700flE+07 2.*240E-02 2=8@@0EtEIl 2.50C10EO@22694101~3 37 2p9000E+07 2,a992E-02 3.000@E+a7 2,13924E-02 3p1000E+07 l,9017QEB02265410103 38 3,20@0E+07 1.7427Ew$?2 3.3f?a8E+0t l,b289E-02 3.40@0E+@7 l,546BE-0226S41~103 39 3,500BE+07 l,a707E-02 3t60@OE+07 1.3871E~02 3p7Bt10E+07 1.3E27Ew0Z26941BlB3 UB 3.0@00E+07 l,RIUZE-02 3.9006E+07 1.137$E-02 4.09kJ0E+Bl l,0609E=9226S410103 41 26S410 ~ a2 2;68SfIf+045.5J65E+01 e e 02bS4101f!7 0 0. 8.4a90E+05 0 : 117265410107 23 2 11! 265410107 ; l;liifMOEWOS 0, j,0ti@@IE+06 la0192Ed l;1000E+O& l,1400E-05265410197 3 l,?000E+96 l,2issE-nS1.3~@OE+06 1.3887E~05 iF4000E+U6 1.51b~E=@5265410107 4 lp5@WUE+0b l,64a9E-a5 lm6@B@E+0b 1.7752E~@5 l,7@00E+0b l,9a66E~@5265410107 5 $p8@0k3E+B6 2,0389E-05 1.90@OE+06 2.1718EoC15 2.0000E+06 2.3V91EW95265410197 6 2,iW6E+06 2,4304E-05 2,2000E+0b i?,5716E*05 2p3@00E+06 2.7@U3E~a526S41@197 7 ?p4@B0E+Iitb ?!,IB364E=05 2.5@0dE+06 2.Q675EQ05 2p6000E+06 1.09?uE-~52b5410107 8 2,7000E+0b 3,i?i159E-05 2.80110E+06 3m3527Ewh5 2p9flnflE+@6 3,4774E*@5Pb5410107 9 3,0000E+06 3,6000E-05 3.la00E+f36 3.7633EvflS 3m2fdC4~E+@6 4,@~J00E-0SP6$41@lr47 10 3p3%06E+06 8,8100EwCf5 3.4@V0E+0b 1.9000Ew04 3,5900E+0b 3,3QlGIE*0dl!654!0107 11 3p6000E+96 5.0000E=04 3,700QE+@b 7.533(4E=04 3.89k30E+@6 Q,609@E=0426541@107 12 3,9600E+0b 1ots3BE~f13 4s0000E+@6 1.1700E093 U,1000E+Mb l,613QE~032654i0!07 13 4p200EIE+fJb l,8900E-a3 4.3@00E+tib 2.200i3Ew03 4.4B00E+@b 2.51@0Em@32654101@7 14 4pS000E+f36 2.76BdE=03 4,60L’0E+06 3,0600E*03 4;700@E+b6 3,3850E=03269410107 15 4p80@0E+@b 3,714UE=B3 4,9000E+0b 4,045tiE-b3 5p13B0BE+Q6 4,390flE*@3Z!b5410107 16 5p2608E+0b 5,0s6DE-B3 S,2500E+06 5.2220Ee@3 5p4000E+06 5.787@E-0526541@lL37 17 SP6900E+a6 b.8820Ew03 5a75@fiE+@b h.@240Ewf13 Sg800UE+Ob 8.454QE-P526541B1B7 18 6p6000E+EIb l,03tIOE=02 6.2aQfiE+@6 lgt3113Ew02 b.2500E+06 l,2850Ew0Z~6541@l~7 b,409@E+06 1.45dtiE-@2 6.60f3tiE+k)6 l,V0612Evti2 6p7$00E+Q6 l,8Q9VE-f322bS4101Gt7 ;; 6p8@00E+~b 1.9660E-f12 7000UaE+@6 2.2u00E-@i? 7,2flfl~E+06 2,5Z7f4E~P22bB41alu7 21 7p25QJtiE+06 2,6000E-F12 7,u000E+Ob 2.8210E*02 7,6000E+0t 3,119@E~02Zb5410107 22 . 7p7500E+06 3,3U90E-02 7.8@fiGIE+B6 3.U13DEW02 8;0000E+U6 3.690kJE-@22b541@107 23 8p2@00E+@b 3.949@E-f12 8.25@0E+ti6 4.fl120Em02 8p4flBBk+Ub 4. 1960E00226f3410107 24 8p6900E+0b 4,G41@E-02 8.75@@E+06 a,b209E*02 Bp80UaE+PJ6 4,678UE-0226!3410107 25 . 9p9000E+Ob 4,60~~JE-02 9.2000E+06 5e@970E~U2 9.25@0Etf#6 5, 141f4EQ0226541010? 26 9P4QW3E+06 5.2SY0E-132 Q,60~flE+@6 5.$730Ew02 9.750171E+f16 5,4u6~E-0226941@lf17 27 9,8@00E+b36 5,&690Ew@2 l.kJPOnE+O? 5.S79UE-02 I.OSO@E+O? 5,86fltiE-P22b541D107 1.199bE*07 6,0600E~02 1.150bE+07 &.i790E~02 1.2900E+0t 603fJ00E~@22b5U19107 ;:

87 6e86tlk~E-022b94 0107 30 7,2~MflE-02265U 0107 31 7,4u8@E-0226!ZU 0107 32 6,19@@E-022b54 0107 33 U,3Ub~lE-@22b54 ,0107 3a 2,2@VkIE-~2265U 0107 35 ? 1.1233E-C22b5U ,FI107 36 6,7t~@tiE-nJ?6s4(3107 37 3,819iiE-@3265U ,tiln7 38 - Z@445UE-f132654 ,BlGj7 39 1,6779E-P326SU Dl@7 40 l,lt)8ZE-032b5u ,ult17 U1 26541Q w- U2 2654 0 n

2;6tMtE+0U 5.5S65E+01 e 0 kWbdl: 1: u 0. ●101197E+07 0 : 39265bl@ 16 2 z 3: 5 265610 16 i l;159#E+07 0, l,15f30E+07 5.f908E=$3 l:200~E+0? 6,6800E-022b5610 16 3 lp2s0@E+~T1.5260E-01 1.3a@~E+a7 2,4970EPBl lt350flE+~7 3,427UEw01265610 16 tra@0aE+07 a.2~90E-81 1.US00E+U7 4m865BE-@l 1.50f3@E+U7 5,368flE~fllZ65610 16 : 1P55EME+07 5,725BEQ01 1.6ROnE+07 S.0830Es01 1.65GIOE+V7 6,173(4E-01265b10 16 b lP700BE+@7 6,f?8ZaEDBl l,75M@E+@7 6.S22flE~fll 1.00@0E+07 6,1U7@E=fllZ69610 lb 7 lP8500E+0? 6,362@Ew01 l.QflflUE+OY 6.3690EQ01 l;95B@E+0? 6,3u9~E~a12b5610 16 8 2p000fM+07 6,3030E-fll 2.1009E+07 6.14QBE-B1 2;2t10flE+@7 5,9410E-kl1265610 lb 9 2p30GMIE+07 5,6850E-01 2.400@E+0T 5c3@U0E-til 2~500@E+Q7 4,8180E?@1265b10 lb 10 2pb000E+07 a.323fiE=fll .2.700f3E+~7 3,857t3EmC?l 2.80@nE+O? 3,U65VE-012656.lB 16 11 2Z90E3BE+07 3,14U5E-01 3.0n0@E+07 2m828ZE-01 3:l@G10E+t37 2,5422Ew@12b5610 lb 12 sp2~00E+07 203B74E-I?l 3.30f10E+07 2,109UE?O1 3p4a00E+@7 1.9297Ec0126!3610 16 13 3,5000E+@7 l,?t)82E-01 S.60QtiE+07 1.b24QE-01 3p7000E+07 l,5027E=0t265610 14 3.80@tlC+B7 l,3s52E-t31 3.900flE+07 1.2898Ew@l 4.D000E+07 l,ZM09EWE1265610 :: 15 26S610 lb i?;60$tE+0fJ 5,~3b5E+01 6 e 0265610 1: 0 0. ●2.0a96E+e7 e e : 21265610 17 2 21 5 269610 17 : 2;0846E+O; 0, 2,100~E+07 1C1817ET04 2.2000E+U7 l,OnOOE-03265610 17 3 ZP300@E+b7 5,?l~0Ew~3 2.U0~~E+@7 1.8D@flEvU2 2.50flflE+@Y 3,Us8J~EW02265610 17 2,6EKME+~? 5,3?00E=02 2.700@E~07 7,2850Ev02 2F800~E+@7 9,03flBE-02265610 17 ; 2,9000E+k37 l,0282E-01 3.0R0aE+07 1C1289E+01 3pl@00E+07 1,1996EvO!26561O 17 6 S.200CJE+Bl i,2380E-01 3.3Qf~@E+07 1.2549F+01 3F400@E+07 1.2552E-O126561O 17 7 3p500@E+a7 1,24B1E-01 3.6000E+07 1.2069E-I?l 3p7FW10E+07 1,1666E-OI26561O 17 8 3.8000E+07 1.l139E-01 3.900@E+07 1.06i2UE~Ol fI.00a0E+@7 l,0~15E-Ql~65610 17 9 Zb5b10 0 10 2;6@SbE+0a 5.53b5E+01 B 0 G!26!3b10 22 u 0. -7,b140E+06 0 ; 59269610 22 2L3 2 5: 22 : 7;7510E+06 $?, 7.80DflE+06 2m8324EB0? 8f000@E+06 l,4393Ew06%::: 22 3 8p200flE+06 2.S9SaE-@6 8.25@@E+0b 2m8844E~@b 8P4000E+06 3,7514E-0tJ2656113 22 4 8p5000E+06 LI,3295E-n6 8.6P~nE.+~6 409fJ75E-@6 ”8.75@@E+@6 5.774bE-@b2b5610 22 8P8QMME+B6 6.k1636E-@6 9mB@@nE+f16 ?.21V3E-ti6 9.200@E+@6 8m3757E-@6~6s61@ 22 : 9,2500E+@6 8,6&47E-@6 9.UO(3@E+06 9.E318Ew06 9.50f10E+@& l,0110EcJ05265610 22 7 9P6FM6E+’36 f,@688E-@5 9.75@CIE+06 1,1555E-U5 9:8GMOE+06 l,18aUE-05?bS610 22 8 lp600$?E+n71,30@@EQp5 1.W5@~E+@7 3.1000E=Oa lp1000E+@7 Qs6b~@E=@0265b10 22 l,lS0@E+07 l,700@E-03 1.2~@hE+@i !.7500E@03 l,25f?0E+072,05@@E-~32b5610 22 1: l,300tiE+07 2,59@14E-a3 1.35@PE+U7 3.Ou@OE-n3 1.~@01?E+137 3,a70VE-f132b561@ 22 11 l,450@E+07 a,06@0E-f13 l,5n@@E+~t 5,230@Ew@3 lp55P0E+@7 70246QIE-a326g610 22 !2 “ lp6@kWE+f37 9,940@Eon3 l,65@aE+07 1.3270Ew02 1.7n00E+07 1.739EE~@2265b10 22 13 lp7500E+07 2,i?050E-08 1.8fl@OE+@7 ?.69f10E*@2 l;85GIflE+v7 3.1730E-f122b5b10 22 la lp900flE+07 3,65VQEWn2 l,95HCiE+07 U.135UE-(72 2.tiG10flE+@7 4,56R~~-P2269b10 22 15 “ 2.1OQM3E+O7 5.$06aE@32 2.200f?E+07 !5.7800Ew02 2:3t3t3nE+u7 6.335L?E-022b5610 22 lb

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90 lb 17 18 19 Z@ 21 22 23 24 25 26 27 28 29 3U 31 32 33 34 35 36 37 38 39

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