SCIENTIFIC ABSTRACT KAZARINOVA, M.I. - KAZARNOVSKIY, D.L.

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• Collection: Scientific Abstracts
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• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: June 13, 2000
• Sequence Number: 1
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

120-4-4/35
AUTHORS: Gorbachev, Y.M. and Kazarinova, M-I
TITLE: 1 1. t if.-
Detection of Disii ration Fragments and Charged Particles
by Thin Scintillation Films. (Registratsiya oskolkov deleniya
i tyazhelykh zaryazhennykh chastits tonkimi stsintillir-
~iyushchijni plenkairii)
PERIODICAL: Pribory i Tekhnika Eksperimenta, 195?~Ollo*4, (USSR).
pp. - 24
ABSTRACT: The aim of the present work was to design a fast
detector
of disintegration fragrients based on an application of tbin
scintillation films. Tne following scintillators were used:
terphenyl anthracene, 2.5 diphenyloxazol in various concen-
trations in polystyrene. Tne obtained solution %as transferred
by means of a pipette on to a glass surface and was then dried
at room,temperature for a number ofhours. After the drying
process, the film was easily detachable from the glass. To
accelerate the drying pro ss the glAss can be warmed up to
50 - 60 C. A layer of UM ~1 mg/cm---) placed in a beam of
thermal neu'jrons was used as the source of disintegration frag-
ments. The layer was placed in a vacuura chamber at a distance
of 5 cm from the scintillation film. All the measurements were
carried out using a photomultiplier collecting 100% of the
uardl/2photoelectrons. Pulses from the photomultipler were fed
into

24.65 CO, 2'?.6 510
S 0
AUTHORS: Kazarinova, M. I., Zamyatnin, Yu. S..,
3`
TITLE: 2.~) and 14,6' mov Nouf:1,c)[1 cvos,~,, seei 1~1?11:3 I.i
I
,)4 o 24 1 .:1 j% 1.
Pu, .1 ru , and Am~ -1 F1 n E, i
A- --13SR
PERIODICAL: Allommaya energlya, 1960, voi k~d`, 1,,!1, .-2,
ABSTRACT: Following recent. Fission t, e file, Is hy
fast, neutrons va rious resea 1 .01 If, I I, ied u es, I I I
an empirical relation bel.wf.-Ai 'he rel-1, !,7(-- fissioll
cr, f,
probabilil-y f = CT c and para lite 4~u r Ne ver 1 he I C S 0
the functional -relation bel.wef.--n V ari rcumber A
(for a fixed atomic number Z) was invesli~ated in some
detail only for the case of' uranium, and thte !,-la,
ex-pt *.ha, f rise,
tween f and Z was no, ~~Iear a*.. all
quit.e rapidly with increasing Z. TO C103C"' 1 3
aatiell, problem and .o gel.. a more r--elclst~ i'(A)
-e1a`1i,.,ns-1~-.-1*P,
:,4(",
the authops exposed Th", r'u, I'Li- and
Card 1/11

2.5 and 14.6 mev Neutron Cross Sec--lons
230 240
Th
Pu
224 -1 24!
and Am Fission. sc.",
PU
,
,
,
Letter to the
Editor

2."- and 14.6 iTlev neut.rons orig er
J i i iL ngv

) Cj ' '
and targets bombardect Uy 11 k,--v Jeu!

T h eregistra-icn of
even'.ls tcclel- plac-1, '~,y :7~--~ans -,I' a

fission chamber
wil.h electron 13 p e

C01-111CInt. of Th and Am "asz
de,ermlred

me I- r I ca I ly, and ha '-. o f P~l i n a t a vP
i

by "Weighing" it In the flux of, '.herrl,a1 -)n S

The content
of Am241 formed in a la;,er resull.ing

frori, its I i i 1~
disin.egration was dF.'.e~rm

'.rhe amoun'. )f
knc,w'n accumulation time. P

Am 24 1isotopes in layers under
invest li7a- i~n was de-

1~ermined by countim4 CL -particles
e~A,.,ed ~-hose

Isotopes. The Fu2L"~ content in the layer was
also

determined from n~vpber of sporiranec~,S fiSSi-,-113,
'

c,,ri
f p 2~1 by ccun-ir" CL -par-tcles fr
and the amount 0 u

1
41 241
2
Am The PU was ais~'
layer
Card 2/11
therinal neutron flux, taking 1,021-) 10 .Darn
for -,.he

2-5 and 14.6 mev Neutron Cross Sections of' T(P46
Th 230, Pu 240, Pu 241 , and Am 2111 Flasion. SOV/89-8-2-11/30
Letter to the Editor
value of the Pu 241 thermal neutron fission cross sec-
tion. For Pu 240 and Pu 2111 various methods used agreed
within experimental errors. Table 1 contains the
results obtained together with the half'-lives used by
the authors during calculations.
Table 1. The characteristics of layers of Isotopes studied.
r -- ----- ---- -----
Icc
....... .. .
1 (3 1 "j t I.,-)
1.2. lo" 1.1i
13,2 111 12" AIII""; SN", 1.011
Am""' L31
Card 3/11

2-5 and 14.6 mev Neutron Croon Sections of
Th 230., Pu 240 , PU 241., and Am :~41 Fission.
Letter to the Editor
Card 4/11
77246
SOV/89-8-2-11/30
The 14.6 mev neutron cross section was determined by
absolute methods. Neutron flux was obtained counting
ct-particles from T(d, n)He4 reaction, while the
background of scattered neutrons was determined per-
forming measurements at different places between the
chamber and the sources. The 2.5 mev measurements
could not be made completely exact, becauSe of the
small counting rate. Relative meanurementsutilized
twin fission chambers which contained at the same time
a material of known fission cross secWn for neutrons
of given energy. Crca b section of Th w3~otake 941
relative to that of Th , and those of Pu- , Pu
and Am241 relatiNe to the U238 fission cross section.
24l 235
For control purposes Am was compared to U . The
2.5 mev cross sections were also compared to those at
14.6 mev by utilizing the relative fission cross see-
tion3 of materials used in the neutron beam monitors:

2.5 and 14.6 mev Neutron Cross Sections of
Th 230, PU 240, PU 4l, and Am"41 Fission.
Letter to the Editor
77246
SOV/89-8-2-11/30
0.13 and 0.34 barn for Th235 and 0.58 and 1.1 barn
for U238 detectors at the respective energies of 2.5
and 14.6 inev. Cross section values are from papers
of Hughes and Schwartz (see reference at end of
Abstract). All 2.5 mev values agreed on the limit of'
errors, and results are given in Table 2.
Table 2. 2.5 and 14.6 mev neutron Induced fission cross sec-
tions crf
of isotopes, barn.

xsotopeg
I
D.r- 6y
Datm P"., 0., f.,y
--- -- ----

-
'Ire

0, 4 1M

I I; -L-0,3
U. 1-5 JAI
Al
:1 2.1; 1A1

1:2 �0.2

Am'"I
1, I)a 1.0, 1,x. (I]

Card /11 rwi.
cm
C,P%% J.et,p.,

F-swi c.~ui2 a..Oaanb an rh4L tj

2.5 and 14.6
mev Neutron Cross Sections of 77246
Th230P Pu 240
,
Pu 241 , and Am24l Fission. SOV/89-8-2-11/30
Letter to the
Editor

In Table 2, Reference Z-A is: V. G. Nesterov, G. 14.
~I

Smirenkin, Zh . eks 'erim.
teor. fiz., 35, 522 (1958);
and Reference Z-B73 is: A. N. Protopopov, Yu. A.

Selitskly,
Atomnaya energlya, 6, Nr 1, 67 (1959). The

authors paid
spec~jj attention to possible mistakes

in the case of Am ,
where the results disagreed with

results of other authors,
but they did not find any

appreciable error. Evaluation of
Results. The 2.5

mev neutron results verify the decrease of
the fission

cross section and the ratio f with the increase
of A

(for fixed Z). The explanation of this is connected

to
the decrease of neutron binding energy, and to the

related
rise in neutron evaporation probability. From

thin standpoint
the practically negligible influence

of pairing'of the
fissionable isotopes on f(A) seems

slightly strange, since it
affects the binding energy

. The authors found also that f is not a single-
E

lued function of Z2/A since., as seen on Fig. A,
VR

each element has a particular f-curve.
Card 6/h

2.5 and 14.6 mev Neutron Cross Sectiono of
Th 230, Pu 240 , Pu 241, arid Am2111 Fission.
Letter to the Editor
77246
SOV/89-8-2-11/.~O
Fig. "A". Relative proba- M_ _J
bility of nuclear fission f
versus the parameter
2
Z /A. o, neutron-induced
fission; x, photofission 0.4
(points o and x taken fromi
_PU ---
Yu. S. Zamyatnin, The Physics
of Nuclear Fission, Supple- 0,2
ment Nr 1 to the periodical
Atomnaya energiya; M. 35 35,S 36 K, S
Atomizdat, 1957, p 27,
corrected by taking into
account newly published fission cross-section data); are
data from the present investiga6ion. Dashed line Shows
approximate f(z 2/A) relationships for various values of
the
binding energy.
Card 7/11

2.5 and 14.6

v ''_
mev Neutron Cross Sections of* 77 2.'! b
Pu 240
Th 230
PU 2111 , and Am 241 Fission. SOV/8()-8-2-11/30
.0
,
Letter to the
Editor

Trying to fit all the curves togetiler
jlsjrjg 7" n/A , at

n / 2, dependence, It became clear to the
authors

that fitting curves of different groups of elements

would require different exponents of n. To fit Th,

Pa, and U, n
should be 1.7; to fit U, Np, and Pu, n

should be 1.2; to fit
Ain 2 It 2with the Pu curve, n = 0.8.

The authors note that the
weaker dependence of f from

Z is apparently connected to the
fact that, in addi-

tion to the Z 2/A parameter, f is
determined also by

the probability of neutron evaporation,
which again

depends on the binding energy of neut ono. 'If one

takes into account that for a given Z /A and the oanic,

pairing, an Increase In Z Is connected to a decrease

of binding
energy (see Table 3) and, consequently, with

an increase of
evaporation probability, it becomes

understandable why one
observes reduced relative f.ts:31on
Card 8/11
probability of
Isotopes of elements with larger Z.
2.5 and 111.6 mov ?Ieutron
230 P40 24 1
Th Pu Pu
Letter to the Editor
Table 3.
cro.,j.,~ "sectiolij ol,
and Ain-; Fi3aion. /10
Neutron binding eneegy in riuclei versus
Z for fixed Z 2 A, ill inev.
Card 9/11
Th"-" 7.1)
1,;j!33
"7 IN 1 7
21
t 5M
It follows that by observing nuclei which have equal
values of F one can exclude the effect of neutron
'B
evaporation and obtain an f(Z /A depending on the
fission process only (see Fig. fl. The 14.6 mev

2. 5 ai Id mev N'~:utron CrDss See! lon:3
230, Pu 240 , Piz 22 11 241
Th and Am Fission.
Lette.- to the Editor
--j-4!
SOV,4~ 9 - 3 - 2 - I
arid S. K. Sokolova supplied the Isotopes arid pre-
parud the layers; 1, As Tinhehcnko and G. M
Kukavadze performed the mass-spectrometric ;nalysis;
Yu. A. Vasillyev and E. I. Sirot-In performed measure-
ments on the accelerating tube; and M. S. Shvetsov,
Yu. A. Barashkov, and E. D. Beregovenkc) helped "alu.,
mea.3' 'wements. There is I figure; 3 tableo, and 8 ref'-
erences, 3 Soviet, 1 U.K., 11 U.S. The U.K. and U.S.
references are: J. Huizenga, Phys. Rev., 109., 148~
(1958); D. Hughes, R. Schwartz, Neutron Cross See! ioriL:,
New York, BNL (1958); D. Hall, T. Markin, J. Ino!F,.
and Nucl. Chem., 4, 137 (1957); R. Leachman, Report
Nr 24067, presented by U.S.A. at the Second United Na4 T--~
Int-ernational Conference fov the Peaceful Uses of Aicm~"c
Energ%Peneva 1958~; M. Studier, J. Huizenet-a.. Phys.
Rev., , 545 (1954
SUBMITTED: August 8, 1959
Card 11/11

-L 30954-66 EPF(n)_~/4)VA(h)/EWT(j. 4QVT(m)jETG(m)_6/&P(t) 1JP(d
"liNI D ' G
ACC NRz AP6013489 SOURCE CODE: UR/0120/66/000/002/0037/0040
AUTHOR: Degtyarev, Yu. G.; Kazarinova, M. I.; Protopopov, V. N.
41-C
ORG: none lb
TITLE: Fast neutron spectrometer using Si surface-barrier
detectors and LOP
SOURCE~( Pribory i tekhnika eksperimenta, no. 2, 19661 37-40
TOPIC TAGS: spectrometer, neutron spectrometry, neutron
bombardment
ABSTRACT: A semicondt On. An spectrometer has been developed
whose sensing
40 eutT
element is a thin film\of L16F sabdwiched between two layers of
n-Si. Neutron bom-
bardment of the film yields the splitting reaction Li6 + n - T +
a + Q, in which the
combined energies of the triton T and the.a-particle equal the
neutron kinetic energy
plus the reaction energy Q. A section of the sensor is shown in
Fig. 1. Allowing
for the loss caused by the g6ld foil, the authors used a figure
of Q - 4.6 Mev for
thermal neutrons and 4.7 Mev for those above 3 Mev energies. The
preamplified
pulses from each counter are si ed, giving an output of about % +
Q, and this out-
put is connected via an expander to the spectrum analyzer; with t
e expander, any
desired portion of the energy spectrum can be observed. Amplitude
spectra of tritons,
a-particles, and neutrons were obtained for bombarding energies
up to 3.2 Mev. De- %1
Card 1/2
2 -1
ACC NRi AP6013489
Fig. 1*Detector construction
I -- Ni dase; 2 -- epoxy filler; 3 gold
foil; 4 -- L16F layer; 5 - n-Si; 6 outputs
to preampe. -
tected pulse amplitudes v9 neutron energies over the test range
showed a linear
relationship. The spectrometer design is recommended as being
reliable and stable.
Orig. art has: 5 figuress . [SH)
SUB CODE: 20/ SUBM DAM 19Har65/ ORIG REF: 003/ OTH REF: 001/ ATD
PRESS
4? 2- 41
Card 2/2

KAZARINOVAp N. F.
KAZARINOVAO N. F. "The Chemistry of 9-oxy-, 9-orinoaryl
Derivatives of
Acridine." Min Higher Education USSR. Ural Polytechnic
Institute imni S. M. Kirov. Sverdlovsk, 1956.
(Disset-tation for Degree of Candidate in Chomical Science)
So: Kni?hnapi Iatopial, No. 17, 1956.

'R1K'"0T'K0
F
24(7) 3
L'Yov. Wavermyt.t ?X'U I BOOX ZXFLOZTATZON 3OV1,1365
Kate x
r1aly
MO okul
nfm
Cc no -Pkt,-o
ron 3P9ctr;.cCv,,y% (?841~re or th '"Pil- t. 1.
110,
pr -To L-vo Vol. I t &I
akogo Wv * loth Aal.t?njon
Intel
T t Qcu1&r 3p*ct
Its, plyo a 1957. 499 roloopy)
Additlonal ';~;? lbl'Vk, P-.4,opo)ooples
3POnsorin, A,*.,
*P*ktrOmkpjj PA. I j 79 AkA4*
rdltorlai Boa* Aser a L et", A- SUR KOIL1.1'. '0
r4' "'*Qh Ed
B 3 -s 34rarquk, T.V.,
labolins' - " Doctor are 0 3.. Aoad*
I f&Y, I.L. Doe, - h~* I (R**P- U., D.
-Or of p4hya1j,.4jr4a.XathtmAtlcaj Sol 004"d),
K=k%`2t. V.A. &4t
ralt,4U. V al or or phyal &them&tl"_
C4WIdat, or CADd4datq 0Al and MaM LL Sciences.
"WIdato or pph7aloal ;;~ or Teola.al S Ofttloal sotinces.
X&theZAt'oja S C-*nC*4 Raysidy. 3.M..
vamIdAte or plvs-*'u ahd MathomAtl GIOU0*51 ii
1 11 10A . Cal rsal 1010yokly. L.K.
C&I'Al Xa-,"Atilml clence
yo., Oat: Of thralaid *noes" Millyenol'uk V 3.
Card 1130 and MR-meet, Gal I'a and "Subn'"A"
IsAo*4.
Babughkin, A.B. -A V
Infrared 30 . . AW L A
Am Surf Pect"st'Pla 3,,,, r - -
C0 ReactIon, of , 0 the Ad,*rptlo.
On AI__ O.U44 "`yl an~ PkttWl Alcohol@ 161
&Idorov# "r. study or 04 F'rous ler
by Mean@ Of IftfArj Ab,or;tloa Speatra
BelenIkLy. L.Z., X. y. jL,
Photo"trl~ Stud, 4atro'
31d0rov T A ITO
the jn~; -0 AM M-M. 3obol~v Z,,tople f
3,,,,tgV*" 3P*Otrum Of 90;i0 Aeld, AMShiltst 'a
ShAYnker. Yu. M. 3P*Gtrg and Tautomerles or
lists-GY6110 Aaing. AQYI&t*d
"Ostovskly. 1. y4.
Igo
40stragooolo sju~*,,* Shenker and
183
Cam 12/30

POSTOTSKIY, I*Ta.; SHHYXMt Tu.T.; WARINOTA N.Y*
S~mctroscoplo analysis of 9-oxyarylacridines. Fis.
abor. no.3t
183-184 157. (KLU 1118)
I' Voaooyuzry7 nauolmo-iseledovatellskl~v
khImiko-farmtnevtidhskiy
institut im. S. Ordshonikifte i UmIlekly
politekhnichaskly insti-
tut im. S.M. Xirova.
(Aoridine--S;*ctra)

AUTHORS: Kazarinova, N. F., Postovsk-iy, I. Ya.
TITIE: On the Tautomery of Acridine Compounds (K ta-a-
il~-7~d--r-~-y~-'. 5c-ys-
dineniy).
On the Structure of 9 - I-- Oxyphenyl) - an(I 9
dine (0 stroyenii 9 - 'z
nov). 47- - o~xxif en~-,I) 1 9
PERIODICAL: Zhurnal Obshche-y Khimii, 1957, Vol. 27, Nr 12, pp.
ABSTRACT: The subject of tho D.-esent publicaticn is tl-
~r L. - 0 r'-Y
structure of 9 - ~,'- - OVphenyl) - and 9 xyc'~ t-~
Disregarding the piesence of phanolrests ii, tlviy --vct~ not
'~cIv.Y.e
in alkalies. Both compounds are difficullt- t.rj :irzi
drochloric acid and in organic a---icts and have a hLip'li
k**) 340), different from 9-phenylacridine, which, ilicugh
wiVi,,i!, hy-
droxile group., melts already at 181~O and can e;~;1--'s
melted in concentrated hydrochloric acid and o-rg~,ni- A! rEg~-Zds
their characteristics both compounds remird ui c-'
formulae). Based on the zomparison witll co-npcur-.& whi-cr, V-,
~z;'-W'
have a phenol- and quino-d structure, the e-a"hQrL3
dines have oxystructure but not oxc- or The sun",-:'s
Card 1/2 assume that the cause of tha weak phenc.l- AT,.,;-
alk&lin-

On the Tautomery of Acridine Compounds. 9 21
On the Struebux,% of 9 OjWphe- nyl) - and 9
of these compounds is the pcesence Df the st-ong intern-'-~-
gen compounds. The new2,v syr-thetize-1 N-meth'..,)-9.
dine is of unstable chara4,,terp
There are 2' figures, I tablej and 8 referen-~-.-,, 3-
ASSOCIATIOM Ural Polytechnic IrL-iti+.utq (Uraj7a~jy
SUBMITTED: November 14) 1956.
AVAILABLE: Library of Congress.
1. Acridines Isomerism
Card 2/2

XURRATOV, D.L; XAZARINOU, N*F.
1- (2-thiedlazolylaze) -2-naphthel (?,,- =70), a new
acid-bass
indicator. Izv, Sib. otd. AN SSSR no.&4~97 '58. (MIRA
11:10)
1.Urallskly filial AN SSSR.
(Indicators and test papers) (Naphthol)

5(2),5(3)
AUTHORS: Kazarinova, N. F., Vasillyeva, 11. L.
SOV/75-13-6-412/21
TITLEt Photo et 'o D termination of Germanium With 9-
1p-(N-Di'metnyl
Amino) - Pheiiyl-2,3,7-Trihydroxy-6-Fl.uorone
(Potometricheskoye opredeleniye germaniya s 9- lp- (N-Zime
tilaminol
-fenil-2,3,7-trioksi-6-fluoroncm)
PERIODICAL: Zhurnal analiticheskoy khimiij 19589 Vol 13, Nr
6, I)P (177-681
(USSR)
ABSTRACT: Among the known organic reagents on germanium, good
experience
has been made with 9-phenyl-2,'~,7-trihydroxy-6-flti,,)rone
(Ref 1).
By adding traces of germanium to the solution of this reagent
in dilute hydrochloric acid, the color of the solution changes
from yellow to orange and a raspberry-red procipitation takes
place. The formation of this precipitate is an obstacle for
the
photometric determination of germanium and must be prevented
by
stabilizers (Refs 2, 3). It is therefore more advisable tc~
alter the properties of the reagent by introducin,3 other
substituents, maintaining the sensitivity and specificity of
phenyl fluorone and yielding soluble compounds with germanium.
Card 1/4 For this purpose, the authors synthesized

Photometric Determination of Germanium With
sov/7r-1:,-6-12/-',1
9-[p-(N-Dimethyl Amino)) -
Phenyl-2,3,7-Trihydrox;y-6-Fluorone-'
9-[p-(N-dimethyl amino)] - pheM~1-2,3,7-trihydrox~,-6-fluorone
by condensation of p-N-dimethyl amino benzaldehyde, with
hydroquinone triacetate in the presence of concentrated
sulfuric acid. This synthesis is accurately described in the
work (in a yield of 52%). The resulting reagent is a red fine
crystalline powder playing to green and having a melting point
of >3000. It is unsoluble in water as well as in the majority
of organic solvents. It easily dissolves in lyes, in mineral
acids when heated or in the presence of alcohol. A method was
worked out for the photometric determination of germanium
vrith
this new reagent (briefly called DAFF). DAFF forms salts with
acids and is stable in dilute acids. In concentrated
hydrochloric acid a yellow precipitation separates, caused by
the formation of a weakly soluble oxonium salt. The stabil-ity
of the acid solutions increases with temperature in
consequence
of the increasing solubility of the oxonium salt. In the
presence of germanium the color of the hydrochloric solution
of
DAFF changes from yellow to orange, in which connection a
maximum of color intensity occurs only by adding a great
excess
Card 2/4 of reagent. The solutions of the- germanium
compounds with DAFF

Photometric Determination of Germanium With SOV/75-13-6-12/21
9-[p-(N-Dimethyl Amino)] -
Plie'nyl-2,3,7-Trihyd'rox'y-6-Fluorone
are stable in dilute hydrochloric acid (1 n) up to a content
of 1.2jrGe02 per ml. They raprasc-nt highly disperse colloids
and follow the Lambert - Beor's law up to quantities of
1 tGe02 per ml. An increase in acid concentration causes a
decrease in optical density of the solutions. With decreasing
temperature the optical density of the solutions increases
considerably; these changes caused by temperature fluctuation
are, however, wholly reversible. At constant temperature,
coloring remains stable for a few hours, the maxim-am
intensity
being reached after 0.5 - 1.5 hours. The measurement of the
optical densities was carried out by :~ M-4! photocolorimeter
with green light filter. The sensitivity of determination
amounts to 0.05t e02 in I ml Of the experimental solution.
G
As and Bi cause no disturbance. Sb (III), Sn (IV), and Mo
(VI)
react with DAFF in much the same way as germanium; the
sensitivity of the reagent to these elements is, however,
considerably lower than to germanium. Detailed working
instructions for the determination are mentioned in the
paper.
Card 3/4

Photometric Determination of Germanium With SOV/75-1,7-6-12/21
9-(p-(N-Dimethyl Amino)] - I'lionyl-2,.5t7-Trihydroxy-6-Fluorone
The authors thank I. Ya. Postovskiy for his valuable
suggestions and advice. There are 3 figures and 4 references,
1 of which is Soviet.
ASSOCIATION: Institut khimii Urallskogo filiala AN SSSR, Sverdlovsk
(Institute of Chemistry of the Ural Branch of the Academy
of Sciences, USSR, Sverdlovsk)
SUBMITTED: June 29, 1957
Card 4/4

EAZARINOVA, N.F.; L&TOSH, Y*I.; POSTOVSKIY, I.Ta.
InvestigatIM the complexons of amino acid derivatives.
Izv.Sib.
otd.AN SSSR no.2t60-70 160. (MIRA 13:6)
1. Ural'sIdy filial AN SSSR.
(Complexons)
(Amino acids)

1-57 1? 9 0 0
8oo63
S/02 60/132/01/37/064
B011YB126
AUTHORS: Poetovskiy, I. Ya , Kazarinova, N. F., Afanaslyeva, G. B.,
Latosh,
TITLEs New Esters of Dithiocarbamic Acidel
PERIODICAM Doklady Akademii nauk SSSR, 196o, Vol. 132, No. 1, pp. 141-144
TEXT: In the publications data on the protective effect of antiradon (AET,
~-aminoethyl isothiuronium bromide (I)) against ionizing radiation 'have
appeared
(Refs. 1, 2). Thus, the authors tried to synthesize compounds with a
similar
structure, namely, 8-aminoethyl dithiocarbamates (II). They have produced
new
carbamates with a non-substituted amino group (IV, V, V-0. They are
formed by
the reaction of ~-chloroethylamine with sodium salts of the relevant
dithiocar-
bamic acids (sodium diethyl dithiocarbamate, -tatramethylene
dithiocapbamate, and
pentamethylene ditbiocarbamate). The reaction producte were obtained as
easily
crystallizable hydrochlorides (Table 1). By using the known reaction
between
amines and quinones, the authors have synthesized now derivatives of
benzo- and
naphthoquinone (VII-XIV) (see scheme). These types of compound have
recently
become recognized as physiologically active, and as new synthetic drugs,
amongst
Card 1/2
W~

MoO
New Esters of Dithiocarbamic Acids S/020/60/132,101/37/064
BO11/B126
other things as antibacterial and antigrawth mediums. The
benzoquinone derivatives
(VII-IX) and the naphthoquinone derivatives (X-XIV) contain
A-aminoethyl-
dithiocarbamate residues, and easily form on the interaction of
free amines Vt'
(IV, V, VI) with quinones in an ethereal solution. They are
red,readily
crystallizing, not easily soluble substances (Table 2). There are
3 tables
and 8 references, 1 of which is Soviet.
ASSOCIATIONi Institut khimii Ural'skogo filials. Akademii nauk
SSSR (Institute
of Chemistry of the Ural Branch of the Academy of Sciences, USSR)
PRESENTEDt January 17, 1960, by B. A. Kazanskly, Academician
SUBMITTEDs December 21, 1959
Card 2/2

KAZARINOVAP N.F.; PODGORNAYA, I,V.
Chemistry of complexono. Report No.lt Derivatives of
iminodiacetic
acids. Trudy Inst,khim. UFAN SSSR no.W03-110 160. (MIRA
1616)
(Complexons) (Acetic acid)
r-,
I- ~

POSTOVSKIY I.Ya.; KAURINOVA. N.F.; AFAKASIYEVAp G.B.;
IATOSH, N.I.
-.Aminoethyl diethyldithiocarbamate. Zhur. VKHO 5
no.1:3-13
160. (MIPA 14:4)
1. Urall.skiy filial AN SSSRj lutitut kl'-4mii.
(Carbamic acid)

SHEYNKMAN, A.K.; KAZARINOVA, N.F.; UBIN) Ye.P.
N-acylpyridinium salts as pyridilic agents in
Fridel-Grafts
reactions* Zhur*MiO 7 no,1:112-113 162. NIRA 15:3)
l..Donetskoys otdeleniye instituta, organicheskoy
khimii AN SSSR.
(P#7idinium compounds) (Priedel-Crafts reactions)

KOLOK)YTSEV, L.R.; KAZARINCIVA, N.F.; 0SONYA, N.I.;
SHEYNKMAN, A.K.
Antibacterial action of some N-substituted py-ridine
derivatives.
Report No.l. HAkrobiol.zhur. 24 no.3:23-28 162. (MIRA
15t8)
1. Donetskoye otdeleniye Instituta organicheskoy khimii
AN UkrSSR.
(PYRIDINE) (BACTERIA, EFFECT OF DRUGS UN)

KAURINOVA R.F.; BABI14, Ye.P.; SOLO&O, K.A.; KOTELMTS,
M.I.;
A.A.; SHEYNDWI, A.K.
PreparatiWi of 4-ethylpyridine. Zhur.prikl-WP, 36 no.3:
649-654 MV 163. (MIRA 16:5)
(Pyridine)

SHEYNKMAN, A.K.; RUDENKO, N.Z.; KAZARINUVAv N.F,;
LYSENKO, V.B.
Structure of quaternary salts of
4-(p-dimethylaminophenyl)- and
4-(p-dimethylaminosiqryl)pyridines. 2hur.ob.kbim- 33
no.61l964-
1969 A 163, (MIIU 16:7)
1. Donetakoye otdolemiye Inatituta organichaakoy khimii
At UkrSSR
i Donetskiy gosudartitvennyy neditsinakiy institut.
(Pyridinium compounda)

KOST, A. N.; SHEYMCMANp Ae K.; LAZARINOVA, N. F.
Interaction of acetylpyridinium salts with dialkyl
anilines.
Zhur. ob. Khim. 34 no.6t2O44-2049 Je 164. (MIRA 17:7)
1. Donetskoyt otdaleniye Instituta organicheskoy
khimii AN UKrSSR
i Moskovskiy gosudarst,irennyy universitet imeni.
Lomonosova.

V.A.; KAZARINOVA R.P.
Temporary disability in skin diseases. Vest. derm. i ven. 38
no.3:71-72 Mr 164. (MIRA 18:4)
1. Ullyanovskiy oblastnoy kozhno-venerologicheskiy dispanser
(glavnyy vrach V.A.Konnov).

,_KAZ~R~NOVA,_V.,_ kand.arkhitektury; FEDOROV, M.,
kand.arkhitektury
Composition; basic categories and regiLlarities.
Tekh.est. 2
no.l2s2-7 D 165.
(MIRA 19:1)
1. Vaesoyuzny)r nauchno-isoledovatellakly in8titut
tekhnicheskoy
eatetiki Gosudarstvannogo komiteta Soveta Ministrov
SSSR.

7
Al
GRXBOV, I.V., inshener; VYAM Aand.tekhn.nauk, red.;
SKYORTSOVI,
--Fm
I.P., red. iZdat el'stTa; STIPANOVA, X.S., tekhn.red.
[Methods of transporting large reinforced concrete panels by
geans
of trucks] Sposoby pereT4)zki krupnorasmarnykh
zhelezobetonnykh
detalei avtomobilIny, transportom. Pod.red.V.M.Kazarinove.
MoskTa.
Gos.izd-TO lit-ry po stroitJ arkhit., 1957. 34 p. (MIRA 10:12)
(Motor trucks) (Concrete blocks--Transportation)

DROBTSHUA, D.V., rod.; CHIZHOV. A.A., voduehchiy
red.: GHN='YEVk,-I.M.,, tekhn.red.
[Geology and oil potential of the Vast Siberian Plain.] Geologlia
i neftenost' Zapadno-Siblrukoi nizoannouti. Leningrad,
Gos.nauchno-
tekhn.izd-vo neft. i gorno-toplIvnoi lit-ry. Leningradekoe
otd-nie.
1958. 273 p. (Leningrad. Yseaoluznyl neftianol
nauebw-lasladovatel'-
skil goologorazvedocbryi institut. Trud7, no.114)
(HIRA 12:6)
(West Siberian I'Lain-Petroleum goology)

KUZIETSOVA, N.P.; KAZARINOVA, V.P.
Geopbysical prospeoting In studying regional
geologloal struoture
of the West Siberian Ple6in. Geol. nefti 2 no.4:11-16
Ap 158.
(KIBA 3.lt5)
1. Novooibirekly-geofixiohealdy treat.
(West Siberian Plain-Proapeoting-Geophysical methods)

WCC-NK AP5022639 ml/oo8g/65/019/002/0179/0100
AMR: Gromov. D. F.; ygrma Ia.
Solodyankin,' M. A.
TITIZ: Angular andenergy distribution of Mmma radiation on the
surface of a iolume souroe 17
SOURCE: Atomnaya energiya, Y. 19, no. 2, 11165, 179-180
TOPIC TAGS: nuclear reactor, gamma radiation, nuclear physics
apparatus
ABSTRACT: Many layers of material are usually placed in nuclear
reac-
tors between the reactive core itself and the outside surface
of the
shield. Thereforep various attenuntion processes must be taken
into
account In calculations of biological shielding. The authors
Investi-
gated the angular and energy d1 Istribution of garuna radiation
on the out-
'he results of their research are given
side surface of the reactor. fl ' I
for two cases. In one case, the reactor vessel wns protected in
water
b
y a boron shield while in the other case no boron shielding was
rovided, The Monte Carlo method vras used for calculations by
means of
-20 electronic computing machinee It was assumed, that the
gamma rays
are generated at the initial einergy levels of 29 31 49 59 6
and 7 Mev6
Mi 539-122!539-121.73:5391121.64
JL/

A Z -C WR -s A-'P- 5-- -0- 2-- -2- 6 3-- -9 0
The greatest statistical error after 12000 tests was less thnn
25% for
angular and 20% for energy distributions, The distributions
applied to
two above mentionod cases and seven energy lavels were
illustrated by
two sets of histogramat The attenuation of 7 Mev gainma.
radiations in
lead shields was also analyzed, The results of this analysis
expressed
in dose rates were tabulated and graphically illustrated.
ASSOCIATION: None
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00 tbil, trials. until Ills hax di,attt ovart conijOrf
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i Drutarmalials with Ima 0.03 N I(CI until (be inall,
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A. Cana On-
Dissertation: "Photocolorimetrie Methods for Chemical Analysis
of Natural
Phosphates and Boron-Containirg Ores." 20110150
Sci Inst for Fertilizers and InsectofungicideB, XJnIstry of
Chemical Inchistry
USSR.
so VeCheryaya M,Oskva
%9.urn 71

Vin
rT
and vres contaWrix bitron.
21
(n), fill ol Nigan,11 (a
fit it-0, 5ofilti"ll :it 1.14 It ii t1trat(d -1,1th
EDTA ;Llbodium Salt) (11~ Ith miltvXiLIC al indi-
,xt~,r, to give tho cc-nuat of Ca. Anothr, I-Itic'm
is titrateil, mith Etiothrome blAck T a, indici,tar,
I. give file stink M ('a alld Vill: NIC Is ollt;lm-I I.).
Pot, tbn duterminatiou of Ca and Mr in
bgritte otirs, the nrt is rxwict~d with ncl, .n, 25
to ~a int -of the rolticn containing I to :Iijing
Ca and IiII; =v trvated kith Aq IM to ppt *tlie
mv4Uioxi,Ics. anti file solution is Zlt~rpd. 'Thi%
solution ils tval,orated to a mfitabte vulame and
Ca and Mg are detcrinined as dtscriN-d alwr.
For the dotetillination of Ca and JAV, In the prestiict-
of phospIliale. e.g.. in apatite, Ca Is dejertinkled hi%t
by decumposing 0-6 g of apalite with 10 ini of 110
if 4 1), Itiltiting to '230 nil. taking a 50-m1 aliquot
JK)rUnn And Wing 0 it 2.5 rm? cif 0- 1 N 1; 1
soluiirm, 10 tu 20 per cent . I% add,,-d to ttvv a 1,11
Of 12 (Ultiveffal tildivatorl, and tbell 0".' to 0.- j;
of 3a, -ator. The ex(m, )f I is d,trt.
in t, tin
(,d bIr t! a lwl larl'o-1 *%' Cacti. Und" i1".
the Cacti[,_%6lUtfo.n.__ --he result is c4lcxllawd ti-ci.
The tota. ! Ca and Mg is determined by vidding 25 nk,
uf 0-1 N :1 to .10 In[ of the acid extrazt. adding I D ml
of a buff,ir Solution lprejwcd 1)), 07g of
.11 ter, f-dding 570 I'll tit tr, jwr c cot ~~tj
tion ai,d d-luting to I lal 0 . mid 9 it, 10
droIA ,f Vrik~Jlx,mw black T I'lle 4;!,,
tion is (Illuttil to IM IDI unit c-im(olly tift-atvd tith
0.1 s A1,;,.;0, Und,r the _nm conditi'lliN. V.', n1l
of 1 sohl lion mr! fitratcd Nvith the Mpot 1, sollition ,
4, Is. ,kit I it
!,arm
Abs Jour: Ref Zhur-Biol., NO 12, 1958,
Author Kazark11ij_2a-Y--_
.-t-
inst of-gTv-en. ing of Karakul
Title on Breading Idork in the Roar
Sheeps,
Orig Pub: Khodzhagii qishloqi Todzhikiston, S. kho
Tadzhikistanal 1957, No 7, 10-12.
Abstract: No abstract.
Card 1/1
39

Concerning the Structure of an
Intermetallic Zr Compound. Brief
Communication
SUBMITTED:
Card 2/2
77122
SOV/70-4-6-23/31
J. Inst. Metals, 86, 504, 1957-1958.
July 21, 1959

`;06
D2 25 /'D j 0 5
A ("j, ;.alkliia, N.I., and Yuz,~-,rncosklly, 3.1.7
In j s~nthesls ol" cyanuric a,-Ld' f.-o!
1, 1 'J'L ~',!.-arnal prikladnoy khimii, v. 34, no. 7, 1961,
1563 - 1587
D, in technical literature do not give the reaction me-
I 12 1.4 the thermal treatment of urea nitrate under atmospheric
,_nd the present work deals with these aspects. With an
of 0,01 gr., 3 gr. of urea nitrate in a glass test tube
hea*-d in an oil thermostats to the required temperature and
J_i tlir_ required time. After this the test tube was taken out,
~_';_'Ied and the contents weighed. Ammonium cyanate was determined
the portions of the product by potentiometric titrntion. The
of the separation method for determining ammeline and
consisted of the alkaline extraction of samples of the
1/5

22h36
5/08 61/034/007/011/016
The eynthesis of cyanuric D223YD305
product followed by the spectrophotometric analysis of ammeline
and ami;iclide (Ref. 27: N.I. Malkina, A.I. Finkel'shteyny ZhFKh
32,
5P 981, 1958). For better clarification of the procesep the sepa-
rate products were expressed as the yield on the initial urea ni-
i-rate via carbon mass balance. To study the kinetics of
formation,
cjmvirio acid was produced at temperature intervals of 132-15000
azil for corresponding experimental times of 15, 30, 60, 120, 180
n,inutss. In order to increase the yield of cyanuric acid and also
to '*ree it from side products a series of experiments were
carried
011t, the results of which are given in the following table:
T,-.-ble. Cyanuric acid and oxyamino products (ammeline and
ammelide)
in the melt.
],~-6end: 1 - content (% on initial urea nitrate); 2 - before HN03
treatment; 3 - after HN03 treatment; 4 cyanuric acid; 5 - amme-
I
-Lina and ammelide; 6 - cyanuric acid; 7 ammeline and ammelide.
Card 2/5

224 6
The synthesis of cyanuric 8/080/61/03.4 007/011/016
D223/D'405
Table.(cont'd)
Cogspmanve xuanypovol xxono7m
N ~O:VxImXXOuPOR~3OAxUX (m mu 0
X5& X &X348nxAs) 2 unaNG
(D cwwpmmm ,wxo=og
0 AD 00 R6 PA WOTWAO
. P="I"M
Epuir"0300 RumnWra a WE"to'. L.1"
45.0 14.21 64.0 0
45.7 131 63.3 0
46.6 MCI 64.0 0
45.6 141 04.1 0
46.0 MO. 64.8 0
44.8 MCI 63.0 0
45j) t4l 64.6 0
44.2 13.0 00.2 0
Card 3/5

22436
S/080/61/034/007/011/016
The synthesis of cyanuric D223/D305
1 table and 27 references: 8 Soviet-bloc and 19
non-Soviet-bloc.
The 4 most recent references to the Englit3h-language
publications
read as follows: H. Iidaj J. Chem-Soc.v Japanp Ind. Chem.
Sect.9
54P 775v 1951; Ch. A., 47Y 1953; H. Iidap K. Vamakawap J. Chem.
Soc. Japan, Ind. Chem. Sect., 57, 587, 1954; Ch. A.P 499 6609,
1955; Z. Voshida, R. Oda, J. Chem. Soc. Japan, Ind. Chem.
Sect.,
56t 92t 1953; Ch. A. 49t 4679, 1955; H. Kinoshita, Rev. Phys.
Chem.
Japan, 25, 34, 1955; Ch. A., 50# 7114, 1956.
ASSOCIATION: Gorlkovskiy politekhnicheskiy institut imeni A.A.
Zhdanova (Gor1ky Polytechnic Institute imeni A.A.
Zhdanov)
SUBMITTED: May 4, 1960
Card 5/5

KAZARNOV3KAYA, B. E.
~
Dissertation: "Shifting
Water Pressure Corditions
Inst imeni Academician 1.
Cand. Tech. Sci.
; 1
of the Water-Petroleum Contact
of a Field." Moscow Order of
M. Gubkin, 3 Jun 47.
and Flooding of Cil Vell,13 Under
Up. Tabor Red Danner Petro2eizz
SO: Vechernvaya Mcskva, Jun, 1947 (P~roject #17836)

K11 ZL1 _117 _'~'KAYAI 1. 7.
;/'. t? f
MM/Oll Wells YAr 194T'
Petroleum - Well drilling
"Movement of Water-oil Interface and Water
Incroachment Into Wells Under Hydrostatic Heat,"
B. F. Kazarnovekaya, 4 pp
TR Acad Sci" Vol LVP No 8
Consideration of an oil reservoir of great length
with a plane oll-bearing stratum, slightly Inclined
to the horizon, and wells drilled at right angles
to it.
P. -,
8T57

KAZAMOVSKAYA, D. B.
Kazarmovskaya, D. B. -- "The Equilibriwa of the
Reaction of Methanal
Synthesis from Carbon Monoxide and Hydrogen at
Elevated Pressure." Moscow
State U imeni M. V. Lomonosov. moscow, 1956.
(Disseration For the DeTee
of Candidate in Chemical Sciences).
So: Knizhnaya Letopis', lio. 11, 19,56, pp 103-114

KA7A.RNOVSKIY, U.S., karA.khtm.nauk-, SIDOROV,
I.P., kand.tekhn.nauk;
,,-Ek7,ARNDV . kand.khim.nauk
Equilibrium of horogenevue gas reactions at high
pressure.
Trudy GIAP no.7:21-25 '57. (MIRA 12t9)
(Phaeov rule and equilibrium) (Onnes)

SIDOROVO I.P.L-KALAMOVSKAYAp D.B.j ANDREICHEV, F.P.
Recirculation flow method for studying the kinetics of
hetero-
geneous catalytic reactions at high pressures. Kin.i
kat. 3
no.4:523-526 Jl-Ag '62. (?URA 15t8)
1. Gosudarstvannyy nauchno-issledovatellskiy institut
azotnoy
promyshlennosti.
(catalysis)

KAZLIMOVSKIY, Ya.S.; KAZARNOWSKAYA., D.B.; SIDal
ov, I. P.
SquilibrIum of homogerjeouo gas mix" reactions
at high
pressure, Khim.prom, no,10.-747-750' 0 162.
(MIRA 15:12)
(Gases)
(Chemical equilibriun)

K"ARNOVSKATA, D. B.; SIDOROTp I. P.; KAZARNOVSI=, Ya. S.
Peteruination of the compressibility of methanol, carbon
monoxide-bydrogen and carbon monoxide-bydrogen--notbanol
mixtures at high temperal-mros and pressures& Eximo prom,
no.3:205-~32 Mr 163, (KM 16:4)
(methanol) (carbon monoxide) (Hydrogen)
(Compressibility)
2
t3i

f.t)T-11~j prit r,,) r
mf~ 4.,j air, C, e

KAZARNOVSKIY, U.S.; KAZARNOVSKAYA, D.B.; SIDCROV, I.P.
Equilibrium of the reaction of methanol synthesis
from carbon
monoxide and hydrogen at high pressure. Xhim. prom.
no.6:
426-433 Je 16). (MM 16s8)
(Wthanol) (Carbon monoxide) (Hydrogen)

KAZARNOVSKIY, Ya. S.; MAHAYLOVA, S.
Aq_!~Z~RNOVSKAYA, D. B.
Influence of pressure on the tberwal effect of
the synthesis
of methanol from carbon oxide tind hydrogen. Khim
prom no. 3:
183-187 Kr '64. (MIRA 17:5)

XATARNOVSKrr, V.D., inzh.,- FAZARNOTSIATA, Z.A-, insh.
Washing salty soils for road construction* Trudy KADI
no,22:
170-175 '58- (MIRA 12r4)
(Soil physics) (Road construction)

PKAZAR SKM-
~NO
They have been teachers from the very
beginning. lUn.nat.
no.1:13-15 Ja 160. (MM 13:5)
(TUNSPIANATION or OR.GKMj TISSUES, RTC.)

AZER111KOV, V.; ARLAZOROV, M.; ARSKIY) F.;
BAKM~IOVp S.; BELOUSOV, I.;
BILENKIN.. D.; VAIELI, I.; VLADDIIROV, L.;
GUSHCHEV, S.;
YELAGIN, V.; YERESHKO, F.; ZHURBINA, S.;
KAZAHNOVSKAYA, G.;
KALIN11", Yu.; KELER, V.; KONOVALOV, B.;
LE:3EDEV, L.; PODGORODNIKOV, M.; RADIKOVIC11) I.;
REPIN) L.;
WOLYAN, G.; TITARENKO, V.; TOPILINA, It.;
FEDCHENKO, V.;
EYDELII~',All, N.; WT) A.; NAWOVp F.; YAKOVLEV, N.;
MIKHAYLOV, K., nauchn. red.; LIVANOV, A., red.
[Little stories about tho great cosmos] Malon'kie
rasskaq o
bol'shom Kosmose. lzd.2., Moskva, Molodtda
gvardiia, 1964.
368 p. (MIRA 18:4)

IL 04311-67- EWT(m)/EWP(t)/ET1 JJP(C) M-~NB
ACC NRa AP6018265 W SOURCE CODE: UR/0133/66/000/002/0171/0173
AUTFORS: Fomin, V. V. (Candidate of technical sciences);
Kazarnovskaya, I, I,
(EngineeO
ORG: none
TITLE: Resistance of martensite and martensite-forrite type stools
to hydro-erosion
SOURCE: Stall, no. 2, 19660 171-173
TOPIC TAGS: alloy steel, - ine equipment, sea water corrosion
ABSTRACT: kho resistance of 10 different martensite and
martensite-forrite types
of steel tJ hydro-erosion was studied. The study was carried out
with the aid of
a magnetostriction vibrator as described by 1. N. Bogachov and R.
L Mints
(Kavitatsionnoye razrushoniye zholezouglerodistykh splavov,,
Mashgiz, 1959). The
rate of motion of the specimen was approximately 60 m/soc and the
diameter was 8 =0
Several specimens were tested under natural conditions in sea
water. The influence
of annealing temperature on the flow impact resistance of the
different stools was
determined. Microstructure photographs of the apecinens are
presented. The experi-
mental results are omvmrized in graphs and tables (sea Fig. 1). It
was found that
the martonsite and martensite-forrite type stools acquire a
higi.141!'
resistance I~F hydro-
erosion as a result of quenching and annealing. Stools ;YJLIODl
OKhl6N4D4T,I-hnd
30Kh14G6T soess high resistance to hydro-orosion and action of sea
water. It is
Card 1/2 UDC: 620.193.16:669. 15-194:669.26
L 04311-67
ACC,NR: AP6018265
Fig. I Destruction curves for steel
18=4VA obtained in hydro-
erosion experiments:
(a) annealed state,*
b) quenched and annealed state.

a

L
LI
~

0
0 12
.'Time from beg ning of experiments, hours
recommended that stools 4KU3. 20Khl3 fgg.8~ and KhlOS2M be used in
the construc.
tion of parts designed to operate under conditions of intensive
cavitation. orig.
art, has; 1 table and 5 graphs,
SUB CODE: 3-1,O/SUBM DATE: none/ ORIG REF: oo5
Stainless Steel

ACC NRt
AP6004175
SOURCE CODE: UA/0096/66/000/002/0083/0086
Dissert'aDt);
AUTITOR: ?0minj V.V.' (Candidate of technical Belences,
"azarnovskaya, Iol. (Engineer)
I
ORG: Murmansk Marine High School (H=anskoe Vysshe morekhodnoe
uchilishcrie)
TITLE: Resistance of high strength stainless ste'els~to the shook-
cyclic action of a water Se ~ /i
SOURCE: Teploenergetika, no. 2, 1966, 83-86
,TOPIC TAGS: wear resistant alloy, high strength steel, stainless
steel,
mechanical shock resistance
ABSTRACT: In the experimental work, the res1stance to failure was
de-
termined in a ~et-shock unit In fresh water, at a rotation
velocity of
the samples of about 80 meters/sea and a diameter of the exit
open 6
zzle of 8 mm,(,' The foll iing type iteel w4e tested-
of the X.
X BT(~1918119T; 1257,hl4Gl -
_lY.h4lND,k OKhlMy__4D2T)"N~414q6T, 'Olhl6~ D4 9 2,
%J A te. __I1_
,lKh16314AT~k2OKh16G14H3AFAand Kh25N5M ble sts the mec
propertia n the resi ce to $f the steels investiGated under
the conditions of the experli-ents.-10was found that the highest
wear resistance.under the experimental conditions was exhibited
by tha
,'Ca-rd -17"2- UDO: 669.15--44:620-193-16

ACC NRs
AP6004175
dispersion-hardened austenitic ste'9~s lXh16G14AT and
201K'hl6Gl41T3AF,
additionally alloyed with gitrogenV~nd the dispersion hardened
steel
OKhl6N4D4T. A high resistance to jet-shock wear was attained by
quenching from 11600C with subsequent aging at 70000 for 10 hours.
The steels investigated are atainlass and have sufficient
corrosion IV
resistance In fresh and salt water. Orig. art. has: 4 figures ahd
3.55-1
tables.
SUB CODE: l1/ SUBM DATE: 00/ ORIG REP: 002/ SOV REF: 000/ OTH
REP. 000
lift
2/2
D'i

A
004
000
00*000000 0*6 0 0
Ilo*******
E-K VIVIF-A 9U Ad A it 9 X 0 0 41 19 0 All lla~q
LLLM-jk-JM-x - A- I , .
Pavia$
T 00

00
The Allowstastic scwU Ali Im#k" of the cald- C--

bids trpe.
IX)V Intl. J Phy.,
Chrn- 20. IM11,

in
'60

t F&tj," C,4d ill till, I&ItkV
its diffin"

4111,1111

F&S Cue.. KOO. II&(h. fe-I
11
NI:1
177
7

-
.
,
.
"I", milli
eo
got
mand 972.5 ki.-cal.jutok,
see
00 j
00,01
:100
eel
Site SLA 411ALLVIROKAL LFTIBATL41 CLASSIFICATION
itim. lill'aliv.
son*" .0 1 salami .10 a.. Gal
AV 00 -jiT". 8 . W I I I I I . p -T
It a ; I
* 0 0 It
0 0 *1* a 0 0 0 0 0 0 0 0 * 0 0 : a
zot
too
too
I I I pw a a 9 1 IF a 9 aw a 3 1 V
0 0 0 0 0 q 9 0 0 a 0 4 a 0 0

oAff I- i-
_- 1_._i .
A
Host of was" gunkm ese" 614 Waited
aWly of Ow sow %Amlo. 0. P. MkWskil. L- J.
"-" t. A. M*jp&m*r'y%u. and 1. A. Kami-
-*.W - a. xwpwfnr.4:brm. lost.. Mowvwi.
lwwl Aw. SMA S.M. . ". TWISOW.-The
bmt of ". of the asomkis K% (pmpd. the action a(
Os on dry KOH sod cift, witli liquid NJ7. in Till. HA0j.
16 4&4.) - KJ% (&q.) + IW +
W+Mimuy to (ST.) AS.. %Cal./nu*;
new, with the aid of kwwo lbermorlmus. dats, The cmlcd.
t of tonnaticis of KO~ from the elements is #12.1 - 11.0
kml./mok. For The down". 2K0, - 21M, + 0,.
Am' - -11.6. AS* - W em AP. - -21 1 bml.:.
Mole. FarThe rameflaus iu;4,7d-I'n*tbv lwrp:of Ko~.
the mecbAu6m XW + OX - X" + Olt Is exchulewl by
the tkfmAyftmk Ws, caW. to All' is 13.4. IV n
-32 Ar. m 111M, sow possible nwekx*Kn involv"
The ;4;=te FICUSwely Koli-(h + Ch - KOs +
0~+1101. The kt;Wof KOmbduganslogoutto that d
KI... te"Usawal of the X.F. type with a - IIJ194. c -
MUS A.. Use lattiot is calcd. to 149 kcul.; brmv.
the clecu 8"Y w"IeT
4 0". rated. to 67 bml.. Eg. 3 thum
the election aftity of Of. IN. Than

Had ad iwoMWi of 1. Xammovska
'a1"1 1. A. Xammy -ICUS776T.'
Moscow). Aw. "22-8(1061).-
hftt of lartuallass AN of (XW + (h
6 CAWI.
d *tqd.SJ=.cfK(h dd-16806
4:m
alilu%. . aaarimuica0y betwva 21 sad 23*. CAw-
refliam am Mao& our uw of KA (2.43%1.
Koll "I) im
mm
KOV.
67A ~6 (111"NOL
obtAined In SaW Wmant with tbev"al GT.5kW-1uwk
311mmum by F.-.W (C.A. 8, 2319) Jtk ft_T& d ----
vmiw eculpti. m Boadan

I -
p
I ~ - 1~,i - ~ -) li-- , I., ~, _ ~ . ~.'i --I--."
KAZARNOVSKAYA,, L.I., kand. khim. muk.
.,:, 1
Catal,vats for the oxidation of hydrocarbons in a krypton concen-
trate. Kislorod 10 no.3:25 157. (MLRA 10:11)
(Catalystv ) Otvdrocarbong)

A e
AUTHM: Xuarnovskays., L.I., Dykhuo, N.M., Nsrinskiy, G.B.
32-11-W60
TITM A Device for the Analysis of Oxygen-Nitrogen-Argon Mixtures
(Usta-
uovka dlya arAlisa. unsay kinlorod-axot-argon)
PMODIMI Zavodskava Laborstoriya, 1957, Vol. 23, Nr 11 , pp.
1387-13M (USSR)
ABSTRAOTt In order to be able to carry out the walysU mentioned
aooumtely,
a devioe is moommended, which in based upon the principle of the
ab-
sorption of oxygen by copper and of mLtrogen by calcium with
inter-
mediate measurements of the pressure of the remaining gas. The
content
of argon and nitrogen can in this o&se be attained with an
aooumqy of
up to 0.02-0.05% at a occoentmtion of < 5%. Though beyond that
analysis up to a content of 80% is possible, accuravy is then
reduced.
The following are the basic parts of such a device: A burette
with a
oapillar,y &rot a U-shaped glass tube with copper and calcium; the
burette k of 30 ml oontent) oonsists of some cylindrical
reservoirs
with oapillaries between them. The glass tubes are sealed by
mercury
with a -anom ter tube. The burette in in a glass vessel, which is
filled with water and is provided with a thermometer. Gas
pressure is
here measured aooording to the mercury oolumn, for which purpose a
Card 1/2 vessel in provided in which mercury ia able to rise
under pressure.
A Derioa for the Analysis of Oxygen-Nitrogen-Argon Mixtures
32-ii-W6o
It is provided with two faucets: one leading to the air, the other
to the pro-vaouum. pumps Absorption of oxygen is carried out in a
Jens, glass tube by meww of granulated copper. Absorption of the
ni-
trogen was brought about in a quartz tube which is filled with
calcium shavings. The gu mixture is oonveyed by means of a mercury
pump. The process of amlyeia is deaaribea and examples of oomputa-
tions carried out are given. There is i figure.
ASSOOIATICK: AUAhtlft Scientific Research Institute for the
Building of Oxygen
Machines (Vaesoy4nyy nauchno-isaledovatel'skiy institut
kislorodnogo
muhinostroyaniya)
AVAIMLIt Libmr7 of Congress
card 2/2

AUTHORS: DiVman, V.V., Candidate of Technical Sciences,
67-0-3-7/18
Kazarnovskayat Lel. j Candidate of Chemical. Sciences
TITLE.- The Prevention of theCarrying-Off of Lye From
Decarbonizers
(Preduprezhdeniya unosa shchelochi im dekarbonizatorov)
PMUODICAL: Kislorod, 1958, fj Nr 3, PP. 35-36 (USSR)
ABSTRACT: In high-pressure o_xyglen apparatus the
purification of air from
carbon dioxide is in the USSR carried out with lye (Yrith
a caustic
soda content of 9.5-10%). It happens on this occasion that
the lye
is carried into the apparatus by the draft of air if an
excessive
quantity of foam foms on the lye. It is said that this
forming of
foam, which exercises a detrimental effect and usmilly
disturbs
the operation of the apparatus, cannot be explainea by the
quality
of or by t4e manner in which the lye is prepared, and
therefore
investigations were carried out in this direction. Four
samples of
caustic mixtures were investigated: 1.) Used (impure)
samples;
2.) Pure samples; -1.) Such as were taken from the upper
part of
the carbonizex, 4. 5 Such taken from the lower Tart of the
carbon-
izer. The results obtained showed in a convincing manner
that the
Card 1/2 carrying away of the lye from the deoarbonizer
into the apparatus

25(6),5(2) Kazarnovsk2y V/67-59-2-5/18
AUTHORS: _a, L. I., Candidate of so
-Mi'mical sciences,-Dykhno, N. M., Candidate of Chemical
Sciences
TITLE: Catalytic Combustion of Small Quantities of Methane
in Oxygen
(Kataliticheskoye szhiganiye malykh kolichestv metana v
kislorode)
PERIODICAL: Kislorod, 1959,,.Nr 2, pp 28-33 (USSR)
ABSTRACT: Small quantities of hydrocarbons are always
contained in the
first krypton concentrate (during the extraction of krypton
from air and liquid oxygen). They were removed on various
catalysts by combustion at 0000. Due to its low degree of
oxidizability, methane forms the main part of these hydro-
carbons. Only a few papers have hitherto been published con-
cerning the process of catalytic combustion of methane in
oxygen. In this article the efficiency of various catalystg
was investigated and the catalysts were selected according
tc
whieh are best suited for the combustion of small impurities
of oxygen resulting from methane and other hydrocarbons.
The authors Investigated cupric oxide, active aluminum oxide
Card 1/3 platinum catalysts, copper-chromium catalystst and

Catalytic Combustion of Small Quantities of Methane
SOV/67-59-2-5/18
in Oxygen
manganese ores activated by silver. OxyCen with an impurity_
of 0.02-0.4 % methane was uced for the investigation. The
diagram of the plant used for investigating the catalysts is
contained in figure 1. First, the gas was purified from
carbon dioxide and then passed throuCh the reaction vessel,
which was heated in a crucible furnace. The gas consumption
was indicated by a rheometer. A small portion of the gas
which had flowed through the reaction. vesoel was passed
through caustic soda in order to determine the quantity of
methane burnt on the catalyst. The other portion is led over
a glowing platinum coil, where the rest of methane is burnt.
The CO 2 content of the gas flowinG out here is determined
by the titrimetric method. The degree of combustion of methane
was measured in dependence of temperature and the gas volume
which had passed through. (FiGs 293; Table 1). Further, the
authors investigated the catalytic activity of manganese
ores activated by silver, i.e. dependent on their siliver
content and grain size. It resulted from all investigations
Card 2/3 that manganese ores with and with no silver content
are

-Catalytic Combustion of Small--quantitien of Methane
SOV/67-59-2-5/18
in Oxygen
the most favorable catalysts. A change in the silver content
affects the catalytic activity only to a small extent. Methane
is completely burnt on manganese ore as soon as a temperature
of 3600, a content of 0-10-0-15 % methane in oxyeen and a
weight rate of flow of up to 560 11h has been attained. At
4000 the rate may be increased to 750 1/h. It resulted
from investigations performed in the krypton plant of the
Shchekinskiy gazovyy zavod (Shchekino Gas Works) with the
assistance of A. A. Mokin, head of the oxygen plant, and
A. P. Podchufarov, head of the krypton plantl that, by use
of a furnace with catalysts filled with manganese ore or
manganese ore activated by silver hydrocarbon, impurities
of the krypton concentrate are burnt already at 4600
(compared with '(800 in the case of alumina catalysts) with-
out deteriorating the degree of methane combustion. There
are 6 figures, 3 tables, and 6 Soviet references.
Card 3/3
3/064/61/000/001/007/0111
B132JB218
AUTHORS: Kazarnovskava, L, I., Dykhno, N. M, Vagin, Ye. V.
TITLEs Burning of methane in mixtures with inert gases
PER10DICALt Khimicheskaya promyshlennost', no. 1, 1961, 29-32
TEXTt The authors have developed an industrial method of
purifying inert
gases obtained in the production of orypton from methane.
Several catalysts
were used to oxidize methane quantitativelys manganese ores
from Nikopoll
and Chiatura, nickel catalysts, and aotivated cupric oxide.
The initial
mixtures contained nitrogen and methane, and some of themalso
small amounts
of oxygen. Also other carbon hydroxides were burned under the
oxidation
conditions for methane. The experimental unit used for this
purpose is
schematically shown in Fig. 1. The catalyst was introduced
into stainless
steel tube (1) and heated in electric furnace (2). The
necessary CH 4 /N2
ratio was brought about by rheometers (3) and (4), and then
the mixture was
conveyed to mixing vessel (5). In column (6), the mixture was
purified from
CO 2 admixtures by means of solid NaOH, and then passed into
tube (1). A
Card 1/7

S/064/61/000/001/007/011
Burning of methane in mixtures... B132/B218
special procedure was applied when the CH 4 content waB less
than 1~. In
this case, part of the gas current was diluted with 0 2 up to a
ratio 10:1;
this was done in mixing vessel (10) by means of rheometers (a)
and (9). Then,
the gas was purified from CO 2' CH4 was burned on a platinum
coil, and then
the CO2 evolved was determined titrimetically. When the CH 4
concentration
was above 1-2%, the gas analyzer BTH(VTI) was used. The
catalysts were
reactivated by N2_02 mixtures, reactivation being determined
from the dif-
ference in oxygen content in front of and behind the catalyst
layer. As
manganese ore is not regenerable, it cannot be used as a
catalyst. A nickel
catalyst loses its activity if the gas mixture contains C02 or
high con-
centrations of CH 4* At methane concentrations below 5A, it may
easily be
used. At a temperature of 500 OC, a volume rate of 65 hr- 1,
and an initial
CH4 content 0f-4-5", the residual methane concentration was
less than 0-5-0-TA
/0
for 10 hr . The use of activated cupric oxide yielded the best
results.
Card 2/7

S/06Y61/000/001/00 7/011
Burning of methane in mixtures ... B132 B218
This catalyst was produced by the method of M. A.
Shpolyanskiy (Ref. 3,
Zav. lab. 19, no. 10, 1166 (1953)). It was composed of a 990
mixture of
GuO and Fe203 (BOA) and kaolin (20A). The experiments were
made at 6600C
and at a volume rate of 65 hr - 1 with binary N2 at a CH4
content of 4-5ci*', and
with ternary N2 (82~'o) at a CH4content of 11~ (02 amounting
to 7%). With one
catalyst, 15 cycles of methane burning and catalyst
reactivation were carried
out. The residual CH 4 concentration did not exceed 0-5%
before seven to nine
hr . After this time, the utilization coefficient of CuO was
about 25~'. The
0
above experiments were made in a pilot plant schematically
shoun in Fig. 4.
At a CH4 content of 9.1j.', the residual CH4concentration
could be maintained
for three and a half hr at 0.24'a if a temperature of 7500C
and a volume rate
of 70 hr:-l were used (Fig- 5)- When the volume rate of 70
hr - 1 was reduced
to 35 hr -11 the residual CH 4 concentration dropped below
0-075',0'. At initial
concentrations of methane of 2.3A and 9.1~46 the residual
concentrations were
Card 3/7

S/064/61/000/001/007/011
Burning of mezhune in mixtures ... B132/B218
0.1-0.2%. A residual concentration of O,5A was attined after
13 hr at an
initial concentration of 2-3%, and after 7 to 8 hr at an
initial concentra-
tion of 9.1%. Then the initial concentration was 0-35~~Op the
residual
methane concentrationdid not exceed 0,0031,4 during 5 hr .
The authors re-
commend the following experimental conditions as being most
favorablet
1
temperature: 700OC; volume rate: 70 hr - , Activated cupric
oxide is the
best catalyst since it warrants a maximum efficiency in
burning of methane
and can be easily regenerated, As P. LIvova and Ye. N,
Razheva took part
in experiments with the pilot plant. There are 7 figures and
5 Soviet-bloc
references.
Card 4/7

Z /06#61/000/001/007/011
Burning of methane ini XixiUil' 09 '-B132/B218
Fig. 1 1 Scheme of
10
laboratory unit tor
bmnin g of methane
Legendt I ) steel
tube; 2) electric N,
lurnace
1 3)~ 4)
9) rheometers; 6 and
11) columns with NaOH I
1 7) water tap; 12) platinum..,..
coil; '13 to gas andlyzer
rM
Card 5/-7 (h

3106416110001001100qlOil
Burning of methane in m xturese'.. B132/B218
Fig. 4s Scheme,lof the-, pilot.,.
- ~ ~)vq
plant; Legends 1 JMdI 8).'
valves; 2) and I I ,rotamete reI
3) CH container; rhbo-.
4
con'ta'ot furnaoej-.:,,-.,,
meter;,&;
6) water separatorl 7) colu~m
for the removal of CO I
2
9) ejectcLrl 10) regulating,:.....
cohtaot galvanometer of-typo-,, I;
mpwnP-64 (MRShohft~-54) a)
50
hydrogen, b)c) to type XTA .
(KhTDK) analyzer.
1''Card 6~7
~UALLLI'.Lu_ ILEH 1 1-11"'
4,)7
U _LL~A
A

i
Burning of methane in mixtures ...
Legend to Fig- 5: Time
dependence of the residual concentra
on of methane during burning with
activated CuO at various temDeratures.
Initital mixture'9.1~!, CH4in IN 2;
- -1
volume rate: 70 hr
x) time, hr; Y) residual con-
centration of CH /Q.
4
S/064/61/000/0011/007/01 1
3132/3-71a
Card 7/7

I P. "S 2
5/061/62/000/010/058/085
B168/BI80
AUTHORSt Kazarnovskaya, L. I., Kraft, D. P.
TITLEi Determination of concentration and 8olubili of mineral
oils in liquid oxygen
PERIODICALt Referativnyy zhurnal. Rhimiya, no * 10, 19t 401,
abstract
1OK92 (Tr. Vaes. n.-i. in-ta kislorodn. mao inostr., no* 2,.
1959, 149-158)
TEXTs A visual fluorescent method is described for determining the
concentration of oils in liquid oxygen. The oil remaining after
evaporating a sample of oxygen is dissolved in dichlorethane, the
luminescence of the solution in UV light is compared with that of
standard samples. The results agree satisfactorily with
determinations
by weight. The solubility of lubricating oils in liquid oxygen was
found
to.be ---0.002 mg/l. VAbatracter's notei Complete tranelation.'~
Card 1/1

-----WAFIiOVSKAYA,,L.I.,, kand. khirrichaskikh nauk;
DYKHNO, N.M., kand.
k.himicbeskik.h nauk
Removal of carbon dioxIda and watsr vapor from krypton
concen-
trates by absorption on synthetic zeclites. Trudy
VIIIIKI,'.!ASII
no.9:170-179 165. (MIRA 18:6)

Av C, v 5
Doxadlhik ov~ctlile. V. G.
Put,illf) 4ud .1-1. A. 7*rl,;Iy
A421 I- - 1~
Di ~=4i~
"CA. and
V
Ix;iul on the 0:1
?I~t vagicj between 0.5 P.-A The
I,r.k i; a ~,uqd:,Irar viah ubrui valional,., 1, ~bly-
5rvcll rt~.rr-~O , amlittrefit%ale
liWe 4- C--;, Of 017 b)tlll-IV~ fl rth--~l
lh~
,LrA enly I
slfolll~ly oxjdl~"', w,tb thr f,mm,.ntj-:3n of uA1,49 from.
pimf.n h unit aria!, jib %r d,.Wc tq,,,d

SHT.Y.AXOV# E.N.; SHROIT, I.G,j GUZv Ye.V*; UZARNOVSKAYAp M.L.
Primary intestinal form of anthrax. Zdravookhrananie 4 no.
1:58-
59 Ja-F 161, (MIRA 14:2)
lo Iz Moldavskogo instituta epidemiologii, mikrobiologii i
gigiyeny
(direktor - N.N. YezhovL4 Kishinovskogo maditsinakogo
instituta
(direktor - N.A. Notemitsanu).
(ANTHRAY.)

BSRKHW. D.L., o sent (Leningrad); ITSKINA, R.S.
(Leningrad);
KAZARNOVSKAYA 0 S. (Leningrad); P&RKHMOVA. A.I.
(Leningrad);
RMD'j?r 9 ningrad).
Treatment of tuberculous maningitis in adults.
Klin.med. 31
no.12:31-36 D 153. (MLRA 7:1)
1. It tubarkuleznogo otdoloniya bollnitey im.
Kuybyshava.
(Tuberculosis) (Straptomycin) (Meningitis)

3 35 8 7
S/204/6i/001/005/005/008
h2d 0 E075/E484
AUTHORS: Bobkov, S.S., Kazarnovskay~kR.Sh..
TITLE. Some problems concerning oxidation of ethylene
PERIODICAL: Neftekhimiya, v.1, no-5, 1961, 661-668
TEXT: The paper gives results of an investigation into the
oxidation kinetics of explosion-safe mixtures of ethylene with
oxygen and nitrogen. The concentration of oxygen was below the
upper limit of flammability, i.e. below 13%. The experiments were
conducted in a flow-circulating apparatus. Ethylene was mixed with
nitrogen and fed into the circulating system. Oxygen was added
immediately before the gases entered the contacting zone. The
catalyst (5 nil of AgO with surface area of 0.3 m2/g) was placed in
a glass tubular reactor (I.D. 22 nun) heated electrically. The VK
oxidation temperature was varied from 200 to 2400C. It was shown
that no diffusion effects existed at these temperatures. For the
mixtures containing more than 33% of ethylene the velocity constant
for the formation of ethylene oxide increases more than 100-fold.
Energies of activation calculated for the formation of ethylene
oxide and carbon dioxide and water were 14.3 and 21.4 kcal/mole
Card 1/4
4

33587
S/204/61/001/005/005/008
Some problems concerning E075/E484
respectively. All products of the oxidation form directly from
ethylene between 1.90 and 230'C. Formation Of C02 from ethylene
oxide is predominant above 230*C. By changing the concentration
of ethylene in the mixture it was shown that the reaction order
for the complete and incomplete oxidation of ethylene is zero
in
the temperature range 200 to 240"C. Reaction of the second
order
is observed for the reactions C,!H4 + 0 = C2H40 and
C2114 -t- 302 = 2C02 + 2H20- As the reaction velocity depends
both
on the content of oxygen and ethylene in the reaction mixture
for
the above reactions, it is impossible to increase the
selectivity
of the process by changing the composition of the mixture of
reactants. Introduction Of C02 into the reaction mixture does
not increase the oxidation selectivity. Concentration of
ethylene oxide has the most marked retarding effect on the
velocity
of' its formation from ethylene, but has no such effect on the
formation Of C02 and H20. Thus the removal of ethylene oxide
from
the reaction mixture greatly increases the selectivity of the
process. The retarding action of ethylene oxide, or its
oxidation
products, results from its irreversible adsorption on ethylene
oxide. This effect is especially visible if the catalyst is
Card 2/4

33587
S/2o4/6i/00l/005/005/oo8
Some problems concerning E075/E484
heated before the reaction at 200 to 2500C in the atmosphere of
oxygen. It was shown that a part of the adsorbed ethylene oxide
can be desorbed from the contact surface in an unchanged state.
Apparently the deactivation process in this case is due to
adsorption of ethylene oxide on silver. The following empirical
equations give the dependence of velocities Wl and W2 of the
complete and incomplete oxidation of ethylene respectively:
klC2
W 02 (6)
CC2H40 + kICC02
k2c2
W 02 (7)
;C C02

3358
S/294/61/001/005/005/008
Some problems concerning ... E075/E484
M.I.Temkin, N.V.Kullkova, A.I.Kurilenko and M.Ya.Rubanik are
mentioned in connection with their contributions in this
field.
There are 4 figures, 4 tables and 5 references: 3
Soviet-bloc and
2 non-Soviet-bloc. The two references to English language
publications read as follows: Ref.3: Shen Wu-wan. Ind. Eng.
Chem.
v.45, 1953, 234; Ref-5: A.Orzechowski, K.E.McCormack.
Canad. J.
Chem., V-32, 1954, 388.
SUBMITTED: MaY 3, 1961
Card 4/4

KAZA VSKIY, A.N., inzh.
Preventive maintenance of painted Burfaces. Trud7
TSNII MPS
no.208sI59-110 161, (HIM 14: 5)
(Railroads-Care-,Maintenance and repair)

XAZARNOVSLIY, D.L.
Creative initiative at the ITR Dmitrov Wt goods
factory. Leg.prom.
14 ro.2:14-17 F 054. (HLRA 7:5)
1. Glavnyy inshener fabriki. (Dmitrov--Knit goods
industry)
(Knit goods industry--Dmitrov)

UZLRNOVSXIT, D.L.
Improving the preparation of yarn for knitting.
Leg.prom. 16
no.5:51-52 My 156. O= 9:8)
1. Glanvyy inslasner DmitrOTOkoy trikotazhnoy fabriki.
(Dmitrov-Milt goods industry)

KAZARNOVSKIT, D.L.
New system of repairing tachnological equipment.
Laq;,prome 18
no.9:9-10 S 158. R& 11:10)
1. Glavnyy inshoner DmItrovskoy parchatochnny fabriki.
(Knitting machines--Maintenance and repair)

e
lb
I oles
6
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ere
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0q S) .
OGP7~ '160
WW nvo
evor olq,~%Jl-
Vp