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Joint Nuclear Research Centre

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Reactor Physics Department

Reprinted from

SACTOR SCIENCE AND TECHNOLOGY

(Journal of Nuclear Energy Parts A/B)

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LEGAL NOTIC:

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This document was prepared under the sponsorship of the Commission of the Europi

mie Energy Community (EURATOM).

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Neither the EURATOM Commission, its contractors nor any person acting on their behalf

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lo — Make any warranty or representation, express or implied, with respect to the accuracy

completeness, or usefulness of the information contained in this document, or that the use

of any information, apparatus, method, or process disclosed in this document may not

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nf orma tion, apparatus, method or process disclosed in this document,

authors names are listed in alphabetical order.

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This reprint is intended for restricted distribution only. It reproduce

by kind permission of the publisher, an article from

"REACTOR

SCIENCE

AND TECHNOLOGY"

(Journal

of Nuclear

Energy

Parts A/B), Vol. 17 ­ 1963, 277­279. For further copies please apply

to Pergamon Press Ltd. Journals Department Headington Hill Hall,

ord (England).

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Wiedergabe des vorliegenden in „REACTOR

SCIENCE

AND

TECHNOLOGY"

(Journal of Nuclear Energy Parts AfB), Vol. 17

­ 1963, 277­279 erschienenen Aufsatzes erfolgt mit freundlicher Geneh­

migung des Herausgebers. Bestellungen weiterer Exemplare sind an

Pergamon Press Ltd. Journals Department Headington Hill

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Ce tiré­à­part est exclusivement destiné à une diffusion restreinte. Il

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le «REACTOR

SCIENCE

AND TECHNOLOGY»

(Journal of

Nuclear Energy Parts A\B),

Vol. 17 ­ 1963, 277­279. Tout autre

exemplaire de cet article doit être demandé à Pergamon Press Ltd. Jour­

nals Department Headington Hill Hall, Oxford

(England).

Questo estratto è destinato esclusivamente ad una diffusione

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Esso è stato riprodotto, per gentile concessione dell'Editore,

da

«REACTOR

SCIENCE AND TECHNOLOGY»

(Journal of Nuclear

Energy Parts A\B), Voi. 17 ­1963, 277­279. Ulteriori copie dell'articolo

debbono essere richieste a Pergamon Press Ltd. Journals Department

Headington Hill Hall, Oxford

(England).

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,

„REACTOR

SCIENCE AND TECHNOLOGY"

(Journal of Nuclear

Energy Paris A\B), Vol. 17 ­ 1963, 277­279. Meer exemplaren kunnen

besteld worden bij Pergamon Press Ltd. Journals Department Head;

ton MU

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E U R 4 4 6 . e

REPRINT

ON THE PARAMETRIC REPRESENTATION OF FAST REACTOR SPECTRA by G. BLÄSSER and E. DIANA.

European Atomic Energy Community - EURATOM Joint Nuclear Research Centre

Ispra Establishment - Italy Reactor Physics Department

Reprinted from "REACTOR SCIENCE AND TECHNOLOGY" (Journal of Nuclear Energy Parts A/B) - Vol. 17 - 1963 - 277-279 pages.

Summary not available.

E U R 4 4 6 . e

REPRINT

ON THE PARAMETRIC REPRESENTATION OF FAST REACTOR SPECTRA by G. BLÄSSER and E. DIANA.

European Atomic Energy Community - EURATOM Joint Nuclear Research Centre

Ispra Establishment - Italy Reactor Physics Department

Reprinted from "REACTOR SCIENCE AND TECHNOLOGY" (Journal of Nuclear Energy Parts A/B) - Vol. 17 - 1J63 - 277-279 pages.

Summary not available.

E U R 4 4 6 . e

REPRINT

ON THE PARAMETRIC REPRESENTATION OF FAST REACTOR SPECTRA by G. BLÄSSER and E. DIANA.

European Atomic Energy Community - EURATOM Joint Nuclear Research Centre

Ispra Establishment - Italy Reactor Physics Department

Reprinted from "REACTOR SCIENCE AND TECHNOLOGY" (Journal of Nuclear Energy Parts A/B) - Vol. 17 - 1963 - 277-279 pages.

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Reprinted from

REACTOR SCIENCE

AND TECHNOLOGY

Journal of Nuclear Energy Parts A & Β

P E R G A M O N PRESS

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(7)

Reactor Science and Technology (Journal of Nuclear Energy Parts A/B) 1963, Vol. 17, pp. 277 to 279. Pergamon Press Ltd. Printed in Northern Ireland.

On the parametric representation of fast

reactor spectra

{Received 5 October 1962)

1. I N T R O D U C T I O N

U P TO the present time, fast reactor calculations have been based on the multigroup approach, starting from basic physical data such as cross sections as functions of energy. For thermal reactors, this method is often replaced by a few­group theory based on integral data. Besides reducing the amount of com­ puter time, the integral approach uses information which usually is more easily obtained by the experiments. In the field of fast reactors many cross­sectional data are still unknown, or at least not known with the required precision. Yet, the integral method was seldom used for fast systems, since it was believed that results obtained in this way for one system do not apply to different systems because of the changes in the spectrum. However, if it is possible to represent the spectrum by a small number of parameters, one can use an integral approach for each parameter configuration and extend thereby the information gained from integral experiments to a large extent.

2. M E T H O D O F A N A L Y S I S

We calculated the spectrum Φ in the centre of a certain number of unreflected spherical uranium fuelled fast assemblies by a multigroup code (ZOOM­7090 version) using 16 groups and

the cross sections as given by YIFTAH, OKRENT and MOLDAUER

(1960). We assumed, heuristically, that the spectrum Φ can be written as a superposition of the normalized fission spectrum χ and a residual normalized spectrum ρ :

Φ = Α(μχ + ρ)

where A is a factor related to the normalization of Φ or the total flux level and α gives the ratio of the numbers of neutrons distributed according to the two different spectra χ and ρ respectively.

The residual spectrum ρ might be characterized in terms of its mean lethargy and its higher moments:

/'„

it = Σ ¡¿¡ρ»

= Σ («,. ­

ay

Pi

where is the value of lethargy attributed to the group ;'. In statistical literature, one often finds the following problem : given the moments up to the fourth, find a distribution curve with these moments. The simplest approach is that using the K. Pearson system of frequency curves (PEARSON and HARTLEY, 1958). There one classifies the frequency curves in eight types according to the values of βχ and β2 where:

ßi = μ*Ιμΐ,

β,

=

μύμ?.

3. R E S U L T S O F T H E C A L C U L A T I O N S We calculated the items mentioned in Section 2 for the following assemblies:

(a) Pure uranium metal assemblies with an enrichment varying between 94 and 10%.

(b) Uranium metal assemblies with an enrichment of 50%, containing sodium up to 50% in volume.

(c) One assembly containing 50% (vol.) Na, 2 0 % steeland 30% uranium metal (50% enriched).

(d) Uranium oxide assemblies with an enrichment between 75% and 2 5 % .

(e) One uranium oxide (50% enriched) assembly with 50% (vol.) Na.

(f) One uranium oxide (50% enriched) assembly with 50% (vol.) of Na and 20 % (vol.) of steel.

(g) Uranium carbide assemblies with an enrichment between 75% and 25%.

(h) One uranium carbide (50% enriched) assembly with 50% (vol.) Na.

(i) One uranium carbide (50% enriched) assembly with 50% (vol.) of Na and 2 0 % (vol.) of steel.

TABLE

1.-Case

-VALUES OF a, a, //„, μ3, μ4, CALCULATED FOR Λ NUMBER OF FAST ASSEMBLIES

/<3 /<4

(a) 9 4 % enr. 75% enr. 50% enr. 25% enr. 10% enr.

(b) 30% vol. Na 50% vol. Na

(c)

(d) 7 5 % enr. 50% enr. 25% enr.

(e)

(f)

(g) 7 5 % enr. 50% enr. 25% enr. (h) (i) 1-327 1043 0-701 0-375 0165 0-759 0-617 2-921 2-917 2-937 3-029 3-251 2-972 2-978 0-771 0-741 0-707 0-708 0-816 0-758 0-757 0152 0194 0-249 0-332 0-483 0-211 0-251 1-667 1-575 1-532 1-668 2-243 1-772 1-780 0-406 3008 0-880 0-341 2-465

0-561 0-416 0-262 0-382 0-249 0-830 0-576 0-331 0-504 0-309 2-965 3-123 3-443 3-222 3-354 3-014 3-107 3-321 3-172 3-243 1033 1-087 1-301 1186 1-371 0-955 0-997 1190 1081 1-255 0-274 0-369 0-634 0-441 0-772 0-319 0-456 0-767 0-502 0-744 2-990 3-508 5-156 4-269 6005 2-634 3053 4-521 3-643 5111

The most striking result has been the relative linearity in the dependence of the parameter α on the enrichment down to enrichments of about 15-20 per cent (Fig. 1) and the smallness of the variation of the mean lethargy and the second moment (Table 1) with the change in core composition. It turned out, furthermore, that all spectra could be fitted by Type I curves of the Pearson system. To give an idea of the 'goodness ol' fit' a comparison between the exact reduced spectrum and such a representation by a Pearson Type I curve is given in Fig. 2 for a typical example.

The expression for a Type I frequency curve is:

= const.

(>+T('-T

where the relation between the parameters ;«„ ιη.λ, «,, a.L and

the moments is given in the Appendix and where .Y is the differ­ ence between the lethargy value // and the mode value, i.e. the value of lethargy for which the distribution attains its maxi­ mum.

Dept. of Reactor Physics Euratom-C.C.R., Ispra, Italy

G. BLÄSSER E. DIANA

R E F E R E N C E S

PEARSON E. S. and HARTLEY H . O. (1958) Biomelrika Tables

for Statisticians—I, p. 79, Cambridge University Press. VIANELLI S. (1959) Prontuari per Calcoli Statistici, p. 1334.

Abbaco Palermo­Roma.

YIFTAH S., OKRENT D . and MOLDAUER P. Α. (1960) Fast

Reactor Cross Sections, Pergamon Press, Oxford.

(8)

278 Lettere to the editors

a i-O

FIG. 1.—As a function of enrichment of: uranium metal (case A) uranium carbide (case B) uranium oxide (case C).

FIG. 2.—Comparison between the calculated reduced spectrum and the fitted frequency curve (case A 94% enriched).

A P P E N D I X

According to VIANELLI (1959), the position of the mode and the parameters of the Type I distribution curve are expressed in terms of the moments by :

where

, , , . 1 μ» r + 2

Mode = a — ζ , 2 μζ r — 2

r = 6 + 3ft ­ 2ft ' Ä = ^ > ­ Α ­ Λ / Λ1.

*· = 5 {' ­ 2 + Kr + 2>Jm + W 5 m + 1)

mj> mj>

al = ~ i = Õ >

mt + m% r — 2

mj> m2b

where

mi + m2 r — 2 '

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CDNA00446ENC

Mm

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