THE SOVIET JOURNAL OF ATOMIC ENERGY VOL. 9 NO. 2
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Vol. 9, No. 2
THE SOVIET JOURNAL OF
August, 1.91
OMIC ENERGY
ATOMHail
.11eprlist
-RANStATE) FOW JA-
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EDITORIAL BOARD OF
ATOMNAYA ENERGIYA
A. I. Alikhanov
A. A. Boehvar
N. A. Dollezhall
D. V. Efrernov
V. S. Ernel'yanov
V. S. Fursov
V. F. Kalinin
A. K. Krasin
A. V. Lebedinskii
A. I. Leipunskii
I. I. Novikov
( Editor-in-Chief )
B. V. Semenov
V. I. Veksler
A. P. Vinogradov
N. A. Vlasov
(Assistant Editor)
A. P. Zefirov
THE SOVIET JOURNAL OF
ATOMIC ENERGY
A translation of ATOMNAY A ENERGIY A,
a publication of the Academy of Sciences of the USSR
(Russian original dated August, 1960)
Vol. 9, No.2 August, 1961
CONTENTS
Theory of Heterogeneous Reactors with Cylindrical Lumps of a Finite Radius. A. D.
PAGE
591
RUSS.
PAGE
89
Galanin .
A Study of the Transfer of Radioactive Materials by Steam and Water and the Chemical
Stability of Deposits in the Steam-Water Loop of the First Atomic Power Station.
P. N. Slyusarev, G. N. Ushakov, 0. V. Starkov; L. A. Kochetkov, L. N. Nesterova,
and V. Ya. Kozlov. .
601
98
The Recrystallization of Cold Rolled Uranium. G. Ya. Sergeev, V. V. Titova, and
L. I. Kolobneva
608
104
Separation of the Stable Isotopes of Boron. N. N. Sevryugova, 0. V. Uvarov, and N. M.
Zhavoronkov
614
110
Determination of Energy Absorption in a Mixed Flux of Fast Neutrons and y -Rays by an
Ionization Method. Yu. I. Bregadze, B. M. Isaev, and V. A. Kvasov.
630
126
LETTERS TO THE EDITOR
"Irradiation Reactor". Yu. S. Ryabukhin and A. Kh. Breger.
637
132
Approximate Determination of the Optimum Thermodynamic Cycle for a Nuclear Power
Station. Yu. D. Arsen'ev and E. K. Averin.
639
133
Approximate Calculation of the Mean Energy of Electrons Produced by y -Rays in an
ionization Chamber. A. K. WaPter, M. L. Gol'din, and V. I. Slavin.
642
135
Investigation of the Behavior of Minerals Accompanying Uranium in the Acid Leaching
of Ores. G. M. Nesmeyanova and N. K. Chernushevich.
646
137
Attenuation of y -Radiation from Volume Sources in Iron and Lead. G. V. Gorshkov and
V. M. Kodyukov.
649
139
Attenuation of y -Radiation from Point Sources in Various Media. V. M. Kodyukov. . . .
651
140
Absorption Corrections in the Backing of the 4/r -Counter. R. M. Polevoi
653
140
Particularities in the Variation of the Capacitance of Irradiated Air-Gap Capacitors.
V. P. Sokolov.
655
142
Application of Neutron Pulse Sources for Investigations in Oil Wells. B. G. Erozolimskii,
658
144
A. S. Shkol'nikov, and A. I. Isakov.
VIII Session of the Learned Council of the Joint Institute for Nuclear Research.
V. Biryukov.
661
146
Atomic Energy at the Czechoslovak Exhibit in Moscow. Yu. Koryakin and V.. Parkhit'ko .
664
148
[Japan's First Nuclear Power Station, see Nuclear Power, 5, No. 47 (1960)
[USA Nuclear Power Development Plans for 1960-1970
[USAEC Financial Report for 1959
Annual subscriptions 75.00
20.00
12.50
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Single article
@ 1961 Consultants Bureau Enterprises, Inc., 227 West 17th St., New York 1, N.Y.
Note: The sale of photostatic copies of any portion of this copyright translation is expressly
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CONTENTS (continued)
PAGE
RUSS.
PAGE?
A 680 Mev Synchrotron. V. A. Petukhov
665
154
A New Ore Dressing Plant in France
666
155
A Facility for Irradiating Personal Film Holders. B. M. Dolishnyuk.
669
156
BRIEF COMMUNICATIONS
671
157
BIBLIOGRAPHY
Reviews of Books and Symposia
672
159
Articles from Periodical Literature
674
161
NOTE
The Table of Contents lists all material that appears in Atomnaya gnergiya. Those items that originated
in the English language are not included in the translation and are shown enclosed in brackets. Whenever
possible, the English-language source containing the omitted reports will be given.
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THEORY OF HETEROGENEOUS REACTORS
WITH CYLINDRICAL LUMPS OF A FINITE RADIUS
A. D. Galanin
Translated from Atomnaya nergiya, Vol. 9, No. 8, pp. 89-97, August, 1960
Original article submitted December 21, 1959
This article presents a consistent theory of heterogeneous reactors with cylindrical lumps of a
finite, but small, radius. The density of thermal neutrons inside a lump and in the moderator is de-
scribed by taking into account the azimuthal dependence. The diffusion theory is applied to the
entire reactor volume. Simple expressions for the diffusion length in the parallel and perpendicular
directions with an accuracy to the first power of the lump surface to cell surface ratio are obtained.
It is shown that the average scattering length for the perpendicular direction depends on the lump
shape. A simple method for determining the diffusion tensor for the case of weak absorption and
large spacing between the lumps is considered in section 4.
Introduction
The theory of heterogeneous reactors with point (more accurately, filament-shaped) lumps has been devel-
oped systematically and in sufficient detail [1 and 2]. The basic assumption of this theory consists in the fact that
the neutron density in the lump and in the nearby moderator does not depend on the azimuthal angle. If we con-
sider only an infinite lattice, the fact that the lumps are not point-like can be taken into account without violat-
ing this assumption [2]. For a regular lattice structure (for instance, for square cells), the resulting accuracy in
determining the thermal efficiency is very high if the ratio of the lump cross-sectional area to the cell area is
not close to unity. The author of paper [3] considered an infinite lattice renouncing the basic assumption, and he
found the corresponding corrections for the magnitude of the lump-effect in the moderator.
In considering a lattice with finite dimensions, the azimuthal dependence of the neutron density around the
lump arises not only due to the effect of the neighboring lumps on a certain given lump, as is the case in an infinite
lattice, but also due to the over-all neutron field gradient. For this, the azimuthal dependence of the neutron field
near the lump can be expressed by the following equation:
N (r, 9) = Ao (r) + A1 (r)cos + A2 (r)cos 29 + . . .
The effect of neighboring lumps in a square lattice of infinite didierisions results in the dependence
N (r, .9) = Bo (r) + Bj (r) cos 49 + B2 (r) cos 89 + . .
i.e., the expansion in this case begins only with the fourth harmonic. The appearance of the first harmonic in
N(r, 9) is caused by the lattice finiteness, and, therefore, this harmonic is connected with changes in neutron
leakage and not with changes in the multiplication constant. Thus, if we form a theory according to which
A1 cos 9 terms will be taken into account, we shall obtain corrections for the diffusion length in the lattice.
We shall henceforth consider a square lattice consisting of a finite, but sufficiently large number of cylin-
drical lumps of finite length. Anisotropic diffusion, which has been considered in a number of papers [4-111 must
arise in such a lattice. In this, many authors did not restrict their investigations to the diffusion approximation ap-
proach and, therefore, their results are more general with respect to this point. Nevertheless, it seems to us that
591
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the method presented here deserves attention, since, in the first place, it represents a consistent development
of the theory of heterogeneous reactors with point lumps, and, in the second place, the simple diffusion approx-
imation equations can be useful as a physically fully justifiable limiting case in formulating more accurate
theories. As far as the author knows, diffusion approximation equations for diffusion in the perpendicular direc-
tion in the case of cylindrical lumps have not been published before.,
The following restrictions are used in the proposed theory:
1. All calculations are performed under the assumption of diffusion approximation, i.e., in the first place,
it is required that the absorption in lumps be small, in the second place, the spacing of lumps must be large in
comparison with the scattering length in the moderator, and, in the third place, either the lump dimensions must
be large in comparison with the scattering length in the lump or the difference between the scattering lengths in
the lump and the moderator must not be too large. It is possible that nondiffusion corrections, connected with
intensive absorption in the lump, can be taken into account by introducing certain effective values.
2. Neutron absorption in moderation is not taken into account.
3. It is assumed that thermal neutron sources are not present in the lumps and that the distribution of sources
outside the lumps is the same as in a homogeneous reactor of the same dimensions.
A simple method for determining the diffusion tensor for the case where the lump-effect is not taken into
account and the lump volume is small in comparison with the cell volume is given in section 4. The obtained
equations can be used for determining 'the moderation length anisotropy (if the diffusion approximation is ap-
plicable).
1. General Theory
Let the z axis be directed along the lump axis, and let the x and y axes be perpendicular to the z axis
along the sides of the square cell. For the sake of simplicity, we shall assume that the reactor is finite only
along the x and z axes. We shall also assume that there are no reflectors along the z axis. Then, the variables
can be separated, and the neutron (thermal and moderated) density dependence on z is given by the over-all
factor az z, which will be thereafter omitted.
The neutron density k inside the lump will be expressed by the equation*
-I-00
Mik) (r, ?) E A(k)/ e? ,
n L
? co
where LI-2 = Lj + a2z. The over-all number of thermal neutrons absorbed by the lump per unit time per unit
length is given by:
(1)
S
Mk) (r, 3c?Di/4
do = 2t ,
Ti
i
(2)
where p is the lump radius.
It is known that, in a lattice with point lumps, the density of thermal neutron sources depends on the
coordinates only because of the reactor finiteness; there is no fine source field structure in the cell (we assume
that the conditions necessary for this are fulfilled). There can hardly be any doubt that this condition will also
hold for nonpoint lumps. Therefore, we shall calculate the density of sources as in the case of point lumps:' ?
27(Q.DiL;
S(r). L, I ,) 11?at
r)2
2
0
- ?4ate 4
(3)
? The quantities pertaining to the lump and the moderator will be denoted by the "i" and "e" indices, respective-
ly. The designations of various geometric quantities are clear from the picture. All vectors are two-dimensional.
? ? The age theory is used here. If we assume that It is not valid, the e-a2 7 factor in Eq. (4) must be changed; it
is only necessary that the neutron field fine structure not be present inside the cell. For the sake of simplicity,
the diffusion anisotropy of moderated neutrons is not taken into account. In the diffusion approximation, it can
be taken into account according to the method presented in section 4.
592
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Assuming that Aok= Ao?ex xk, after summation,* we obtain:
271Q. D iL!
S ( *) = a2L2 i(*)
(4)
r2
where a2 4 + az; is the lattice spacing. The IV (r) = (4 T)' exp ? ). function in Eq. (3) is
normalized in such a manner that the integral over the entire volume is equal to unity. However, we assume
that there are no sources inside the lump. Therefore, the regular W(r) function, obtained by taking into ac-
count the lump finiteness, must be normalized in such a manner that the integral is equal to unity only over
the moderator surface. Hence, it follows that, in the right-hand side of Eq. (4), the (1-c)-1 factor must be
introduced, where
7.[Q2
=
The neutron density in the moderator is
AT e (P), = N (r) N2e (r),
(5)
(6)
where Nie (r) is the solution of the nonhomogeneous equation (4) for sources and N2e (r) is the homogeneous
equation solution. By using Eq. (4), we readily obtain
rie-2,t2T A(L)/ O
N "(r k ' * k) = (1 + a2I,F) go(2 " ? '\ )eittxr4 cos h
where
Io =
1?cC taC'?
0 ,
) / ?) ?
1 Q
e
(7)
(8)
In Eq. (7), rk is the distance of the given point from the lump center k (see figure). By expanding this
equation in a Fourier series, we obtain:
150 = (1+a2/ 2) ( A(k)/ X (A-) E r
? x k e
71-=
The solution of the homogeneous equation can be written thus:
N2e (rk,0a) = E E B()1(L)e?i"?A"
fl=?co '
(9)
(10)
where L'e-2 = + a2z; E denotes summation for all lattice lumps including the kth lump; in this case, Rkke
k'
is equal to rk.
By using the addition theorem [12]
r.1_12;.
n(r einap
Le
and the relationships between angles IT = xk,?; = 11) we obtain
+00
N20 (r, 0) = E e?i"ftun (r),
71= ?co
It is assumed that the number of lumps in the reactor is sufficiently large; paper [2] describes how this sum-
mation is performed.
(12)
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Diagram explaining the mutual position of
the k and k' lumps.
where
? (r) = 13K ? (7?Fr )H
,
E (_ i)" 11'
/11=-4?,C0
(13)
ei 01-1,1)
L'e )
where the kth lump is conventionally taken as the 0th lump
r -== ro, rk,= rok,, X0k and E' denotes summation
with respect to le under the condition that k' 0.
The limiting conditions
are valid for each harmonic separately, i.e.,
(
A?in 77") Ile
(1+ a2L,) g0(2
e ?rt Deaxic?a2T
Li n ? t
q0Y
, X
Ni (Q, it) =
Ajo
A I )
0 1
Are (Q, 0); Di aAr
=
(14)
(15)
aN (r
D
ear
ofr,
I
\
n kv/7
e
,r?Q
Jn (as) + Un (Q);
. ?? , D, u,
1
n k a ?NI 1-- ,
Le
where the prime denotes the derivatives with respect to the argument of the corresponding Bessel function. The
(10 (k)
system of equations (15) makes it possible to determine the An and Bn constants.
2.Small Lump Theory
Hereafter, we shall consider only the first correction to the theory of point lumps, and we shall assume
that Aflk) = 41() = 0 for I n I 2. The solution of the system of Eqs.(1.5) will be given by an expression of the
following form (it is assumed here that the lattice is sufficiently large):
== jh,B = 1. (16)
By assuming that n = 0 and eliminating Ao from the system of Eqs.(15), we obtain the characteristic lattice
equation [hereafter, Jn (a,p) is replaced by the first expansion term for cc, p ? 1]:
where
_a2t Li2
( cot r.,2
_i_a24: 1? c ? goV G'
= 23t/4 L2 Q ?
ci o(Q)
Here, U0 ( p) also contains the unknown Oil coefficients. For their determination,
system of equations (15) for n = 1. Let us introduce the following notation:
U.1+ U1= 2W1; U +1? II _1= 2W2
a2 (1? c) (Q)
and
B?.= ;
594
(17)
(18)
we must consider the
(19)
(20)
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where
where
Equations (15) yield:
De Q 1
-767 L'e 2Q-1 W; (Q) Wi (Q)= D e Q I Ty,
ne?a2t
C = (1 De 1' ') 1+ a24 LI,L,;2 1?c
Di 2Q-1
ie?a2T calLg Li2
1?c TL
By using Eqs. (13) and (16), we obtain
x ti ? y(E0H-E2)?yi 221:
x [21- yi (LH- E2)-- v
o= K (IT) -I- I (IT) X [E ? 2iy Ei? 2y 21],
el'it cos K L
(r k) ?
'eiaxkK ? ? E _ ,
0? LI 0 -1. 7
e
= eiaxiz cos 2X K2 (rk 2
k -
For reasons of symmetry, it is readily found that
? ?
? Z2 ?
1 iejaxh sin x K (r k );
lc 1 iT
elan, sin 2X K. (---7r k ? .
L
(21)
(22)
(23)
(24)
(25)
Then, the second of the Eqs. (21) yields yi = 0, and the first makes it possible to determine y in the follow-
ing manner:
[ii (ID] 21+[K1( /-1-) 11 a)] axL:C (26)
L;
\ e I
where
De
s = DE- (2Q? lr'.
For p ? 1, the Bessel functions in Eq. (26) can be expanded in the series
iv
axl4C (1? 2
2 E 0)
(s ? 1)
1
Q2
2 .?
n2
C
? s+ 2/42 (s-1) (.111
(27)
(28)
Let us now calculate the sums (24). The sum E0 can be calculated according to the method described in
(21. As a result, we obtain:*
*It is assumed that
I
=
2rcL/e2
O 4aL
a2 ( I -4- a1/42) '
1,78a 6 '
in 6
21tLF aa
1, < 1.
a2 21t
(29)
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The E1 and E2 sums can be written as
= ' ki sin axak K 17 1,1)
? r I
Z.1 Z-J h2 kl+ki
/ = (k?/4)Cos Kk2, .
2 14,
/to
(30)
(31)
In calculating these sums in the first approximation, the summation can be replaced by integration from ?co to
co with respect to ki and k2 (including the k1 = 1 E and the perpendicular diffusion coefficient is
-7k I F
, t
2 (t?s)i
-Fs j ?
(66)
Equations (63), (64), and (66) coincide with Eq. (49). In the same manner, it can be shown that, in the
case of spherical lumps, the diffusion coefficient is
D c 3 (1 8)]
e s ? (67)
The obtained equations are valid in the first order with respect to c. For this approximation, the diffusion
coefficient depends only on concentration c. If the concentration increases, the field *acting* on each lump
differs from the *average* field in the lattice, and, generally speaking, the average diffusion coefficient depends
on the lattice structure.
The author is indebted to B. I. Il'ichev, N. I. Laletin, and Ya. V. Shevelev for the discussion of this paper.
LITERATURE CITED
1. S. M. Fainberg, Transactions of the International Conference on the Peaceful Uses of Atomic Energy,
Geneva, 1955 [in Russian] (Izd. AN SSSR, Moscow, 1957) Vol. 5, p. 578.
2. A. D. Galanin, Theory of Thermal Neutron Nuclear Reactors [in Russian] (Atomizdat, Moscow, 1959).
3. Ya. V. Shevelev, Atomnaya Energ. 2, 3, 217 (1957).?
4. D. Behrens, Proc. Phys. Soc. A62, 607 (1949).
5. B. Spinrad, J. Appl. Phys. 26,548 (1955).
6. Ya. V. Shevelev, Atonpaya &erg. 2, 3, 224 (1957). ?
7. L. Trlifai, Atomnaya Ener4g. 2, 3, 231 (1957).?
8. V. V. Smelov,AtomnayaEnerg. 6, 5, 546 (1959).*
9. N. I. Laletin, Transactions of the Second International Conference on the Peaceful Uses of Atomic Energy,
Geneva, 1958. Reports by Soviet Scientists: Nuclear Reactors and Nuclear Power Engineering [in Russian]
(Atomizdat, Moscow, 1959) Vol. 2, p. 634.
10. P. Benoist, Rapport S. P. M., No. 522, Saclay (1958).
11. B. Davison, J. Nucl. Energy. 7, 51 (1958).
12. I. M. Ryzhik and I. S. Gradshtein, Tables of Integrals, Sums, Series, and Products [in Russian] (Gostekhteorizdat,
Moscow, 1951) Equation 6.540.2.
13. L D. Landau and E. M. Lifshits, Electrodynamics of Continuous Media [in Russian] (Gostekhteorizdat, Moscow,
1957) p. 63.
*Original Russian pagination. See C. B. translation.
600
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A STUDY OF THE TRANSFER OF RADIOACTIVE MATERIALS
BY STEAM AND WATER, AND THE CHEMICAL STABILITY
OF DEPOSITS IN THE STEAM-WATER LOOP
OF THE FIRST ATOMIC POWER STATION
P. N. Slyusarev, G. N. Ushakov, 0. V. Starkov, L. A. Kochetkov,
L. N. NGsterova, and V. Ya. Kozlov
Translated from Atomnaya fnergiya, Vol. 9, No. 8, pp. 98-103, August, 1960
Original article submitted November 23, 1959
An important problem in the design of boiling reactors or reactors with boiling and super-
heating of the steam in channels is the study of the level of contamination of steam by radio-
active materials, generated and directed into the turbine, the physicochemical properties of the
radioactive deposits and the possibility of deactivation of the internal surfaces of the pipes and
turbine.
At the first atomic power station, studies were made on the transfer of radioactive mate-
rials by steam and water in the loop built into the first circuit of the power station. A deter-
mination was made of the coefficient of deposition of the materials on the internal surface of
the pipes, and the chemical stability of the deposits was studied. Studies were made on prob-
lems of deactivation of some parts of the steam power equipment of the station.
Introduction
It is well known (1-31 that the radioactivity of steam in boiling reactors with nuclear superheating, due
to the entrainment of radioactive materials in the boiling zone, can be about 0.0150 of the level of radioactivity
in the boiling water. However, this value depends to a considerable extent on the type of reactor-operation and
the design of evaporators and separators. The radioactivity of steam caused by activation of impurities in the
steam when it passes through the active zone (7- = 0.02 sec) is very small in practice. It is difficult to calculate
the radioactivity of steam caused by washing out active corrosion products and deposits from the internal surface
of the circuit, especially for certain systems and unstable operation of the installation. The oxygen radioactivity
of the steam was not taken into account.
Description of the Installation
The steam-water loop [4] consisted of two circuits of 1Kh18N9T stainless steel (Table 1), insulated from
one another and mounted in the reactor of the first atomic power station (Fig. 1). The coolant was regular
distilled water. The heat source was provided by heat-evolving elements of the reactor channels of the atomic
power station.
The working channels B I of the circuit were cooled by water which passed through the heat exchanger 1
and was further cooled in the cooler 2, and the working channels A II of the circuit were cooled by steam super-
heated to the given temperature. The coolant was circulated by the circulation pumps 3 and 4. The steam ob-
tained in the vaporizer 1 was directed to the steam superheating channels (SSD) and then through a heat exchanger
6 and cooler 5 they were returned to the vaporizer.
601
Declassified and Approved For Release 2013/02/14: CIA-RDP10-02196R000100060002-6
Declassified and Approved For Release 2013/02/14: CIA-RDP10-02196R000100060002-6
TABLE 1
Characteristics of Circuits I and II of the Steam-Water Loop
Parameters
?Pressure, atm
Flow of coolant, ton/hr
Volume, m3
Pressure drop along route, atm
Number of channels
1.d
.41???
Fig. 1. Arrangement of steam-water loop. Samples
were taken from the following points: a) from feed
tank; b) from the head of pump I of the circuit;
c) from the vaporizer of circuit II; d) from the in-
let to the steam superheating channel of circuit II;
e) from the outlet of the steam superheating chan-
nel of circuit II; f) from the suction side of the
pump of circuit II; g) from the head of the pump
of circuit II; h) from the suction part of the pump
of circuit L
Circuit I
95-100
10
0.33
11
10
Circuit II
40-60
1
0.61
11
3
The first and second circuits of the loop were fed
with di?tilled water 7. Two systems were investigated:
with superheating of the steam (working channels) and
without superheating of the steam (blank channels). The
water temperature at the inlet to the SSD was 265?C, at
the outlet it was 310?C (with steam content of 250/0) and
in the case of superheating of the steam? at the inlet
275?C, at the outlet-340-365?C.
Points for the removal of coolant samples were
placed along the routes of circuits I and II of the loop.
The samples were taken with a steady system. The
places where samples were taken along the circuits of
the loop are designated by Latin letters (see Table 2).
In each sample of the coolant, measurements were
made of the B and y activity, the amount of dry residue,
pH of the medium, studies were made of the radioisotope,
anion and cation compositions of the impurities.
Transfer of Radioactive Materials by Steam
and Water
The transfer of radioactive materials by steam and
water was studied from the change in level of the radio-
activity of the dry residue along the route of the loop.
Samples of the coolant were taken regularly over a long period of time. Table 2 gives the results of measure-
ments on the level of radioactivity of the coolant along the route of circuit II of the loop during various periods
of operation. The periods are due to the fact that the operation of the loop was interrupted or was changed to a
different system. In the first and second periods the steam passed through channels without superheating the steam;
in the third and fourth periods it passed through the channels with superheating of the steam. The days were counted
from the day when a stable system was established. The system was changed over to steam by gradually replacing
water in the SSD by steam [5].
In the initial period when the loop operated on steam the radioactivity of the dry residue of the coolant
at the outlet from the SSD was much greater than at the input. This difference is gradually reduced since the
deposits or corrosion products are washed out. Deposition takes place during this period at the section of outlet
from the SSD?the suction part of the pump of circuit II; the radioactivity of the dry deposit at the suction part
of "he pump is less than at the outlet from the SSD. This difference is also gradually reduced. These phenomena
are caused by the change in rate of elution and precipitation of deposits in the loop, and also by the change in
quality of the coolant. Before exit into the steam system in the working channels, water was circulated with a
602
Declassified and Approved For Release 2013/02/14: CIA-RDP10-02196R000100060002-6
Declassified and Approved For Release 2013/02/14: CIA-RDP10-02196R000100060002-6
TABLE 2
Radioactivity of Dry Residue of the Coolant in Circuit II of the Loop, 10-8 C/kg
Points of sanr
pie removal
Periods
first I second
2 3
4 I 5
third
days
fourth
2 3 4 5
5 6 7 10 11
d, e
e, f
2,6
3,2
2,8
+0,6
-0,4
7,0
19
7,1
+12
-12
3,8
5,3
3,3
+1,5
-2,0
3,6
4.5
amples
not taken
+0,91+0,2
ample
not taken
2,8
3,0
were
s were
19
41,0
14
+22,0
-27,0
2,9
9,2
4,6
-1-6,3
-4,6
1,0
3,2
2,5
+2,2
-0,7
1,4
3,6
3,3
+2,2
-0,3
2,1
2,8
+0,7
1,0
1,7
2,4
+0,7
+0,7
0,5
0,8
1,8
+0,3
+1,0
2,5
1,7
4,1
-0,8
+2,5
(3,0
2,1
38
-3.9
+6.7
Note. The accuracy of measurements was ? 0.1 ? 10-8 C/kg,
41I
Fig. 2. Relative changes in radioactivity
AI of a dry residue of steam and water in
relation to the time of operation of the loop:
1) difference in radioactivity of the dry re-
sidue of steam and water at the points d and
e; 2) the difference in radioactivity of the
dry residue of steam and water at the points
e and f; 3, 4) the curves for difference in
radioactivity with fluctuations in the quality
of the steam.
higher content of salts, which were deposited on the walls of
the channels. Since the steam has a lower content of salts,
in the steam system the prevailing process is the elution of the
previously settled deposits. The contaminated steam, passing
the section of outlet from the SSD-the suction part of the pump
of circuit II, loses a part of the previously washed radioactive
deposits, as a result of which the radioactivity at the sampling
point f is reduced. With the passage of time, these selective
processes are retarded and dynamic equilibrium should be estab-
lished between the content of impurities in the coolant and
deposits at the inside surfaces of the loop. Figure 2 shows the
experimental curves representing the change in difference of
radioactivities of the dry residue of the superheated steam and
water in relation to the time of operation of the loop. The
symbol Almin represents the increase in radioactivity due to
activation of the impurities or due to elution of the corrosion
products from the channels of the active zone. With changes
in the quality of steam, the curves can assume the form of
curves 3, 4 of Fig. 2.
The Physicochemical Factors of the Coolant
in Circuits I and II
These factors are given in Table 3. The radioisotope
composition of impurities in the coolant of the loop circuit
and the first circuit of the atomic power station are the same.
The radioactivity of water in the evaporator during blow-
ing is reduced from 5 ? 10-8 C/kg. The radioactivity of the
steam is - 10% of the radioactivity in the evaporator (the
entrainment factor is 1 ? 10-1).
The entrainment factor obtained in our experiments is 100-1000 times greater than the factors given in (61.
This is due to the features of design of the evaporators and separator and to the fact that in our experiments the
concentration of active impurities of the water in the evaporator differs considerably from the activity of solutions
described in [6].
603
Declassified and Approved For Release 2013/02/14: CIA-RDP10-02196R000100060002-6
Declassified and Approved For Release 2013/02/14: CIA-RDP10-02196R000100060002-6
TABLE 3
Physicochemical Factors of Feed Water and Water of Circuits I and II of the Loop
Point of sample
removal
Dry residue,
mg/liter
Total a and
Y activity,
10-8 C / kgotal,
pH
Concentration of ions,
mg/kg
Concentration Of
chromium
CO2
NO;
Cl'C
mg/kg
Cr,
5,04'
Cr*3
% '
Feed water
Water of circuit I
1 '
Water of circuit H '
0,9-1,3
2
{ 4',2
( 1,3-2,1
0,6-1,1
6
0, -1,1
0,6-1,1
1
1 0,6-1,1
l
0
220-2200
500-5000
5-50
1-7
0,5-19
3-7
3-5
6,2
5,4
5,2
5,2-5,8
5,4
5,4
5.2
5,5
0,6
0,9
0,9
0,9
0,9
0,9
0,9