SCIENTIFIC ABSTRACT BARONENKOV, A.V. - BARONYAN, A.G.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R000203710010-7
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: June 6, 2000
• Sequence Number: 10
• Publication Date: December 31, 1967
• Content Type: SCIENCEAB

BLWgr-,.N'KOV. A.V.j, kazid.t-Ahn.nauk-
Improvement of plarininj and stiniulation of in bonuses
on
the part of miners. Gor. zhur. no.3&15-..19 M~r '63.
3.,-, : /.)

RAMEMOV) A.V.
Improvw,ent of plapning ard workers' material
incentives in
the mining industry. Prace mzda 11 no.9t423-427
S163

MIM'UWV, I?.. BARONXInMV, Ye.
Snvon high prizes out of ton. Must.ujl. 8
no.3:25-26
Mr 15 9. NIRA 13.- 4)
(Bruyellez-Exhibitions) (Coal mining
machinery)

BAROURTSKIY, P. I.
1%" 7, of the White ~qLIBE;iajj s.S.IL Zdrav. Belor 5
ro.l:
25-27 Ja '59. (MIRA 12:7)
1. Predsedatell TSentrallnogo komittta Obahchentva
Krasnogo Kresta
BSSR.
(WHITE RUSSIA--RF.D CiOSS)

EXCERPTA MIN See 4 Vol 12/6 Yled. Yicro. June 59
1778. CULTURE OF A LARGE VIRUS. ISOLATED FROM
NEWBORNS DYING
FROM ENCEPPALO-PNEUMONIA - Culture d'un virus.1
grandes dimensions
isolL% a partir de nourissons morts
d'encephalo-pneunionie - B a r on i V.,
Museteanu C. and Museteanu V. Hop.
d'EnfantsCotr6Z-Cn-r-Llu,:irest-
C. R. SOC. BIOL. (Paris) 1957, 151/10
(1690-1692)
From various organs of deccued newborn infants
an agent was isolated which was
pathogenic for hens' eggs and mice. It measured
0.2-0.3m. It probably belongs to
the lymphogranuloma-psittacosts group ct~
viruses.
Frenkel - Amsterdam (L, 4, 7)
4,

/ I/ ".., -1.1, 1 , -/I - I"I
ANDRWESHCHN, Te.A.; BARONI, Ye.Te.-. KOMRZIMA, K.A.; FANI, I.M.;
RDZYAN,
Plastic scintillators based on polystyrene. Prib. i tekh.
eksp. n0-1:32-34 Jl-Ag 156. (MIJU 10:2)
(Scintillation counters) (Styrene)

21(6)
AUTHORS: Selinov, I. P., Grits, Yu. A., SOV/89-5-6-17/25
Khulelidze, D. Ye. X-.9
Bliodze, Yu. A., Demin, A. G., Kushakevich, Yu. P.
TITLE- New Isotopes of Antimony (Novyye izotopy surlmy)
PERIODICAL: Atomnaya energiya, 1958, Vol 5, Nr 6, pp 66o -
66o (USSR)
Sn 112 (52,3 %), Sn"'(57.2
ABSTRACT: An enriched tin preparation I
was bombarded with 10 MeV deuterons. Two hitherto unknown
activities with 7,0 � 0.5 min and 31 � 1 min half life were
measured. In both cases the 13 +
.L -limiting energy (measured by
the absorption method) amounted to 2 MeV.
Chemical separation of both activities showed that antimony
isotopes were concerned. The probable reactions are
112 113 114 115
Sa (d,n)Sb and Sn (d,n)Sb
The decay scheme is at present being further investigated.
SUBMITTED: September 4, 1958
Card 1/2

New Isotopes of Antimony
SC)V/89-5-(,- 17/21)
Card 2/2

BARON-I. Ye.Ye.; SHONIYA, V.M.
Ag(Tegate state of luminescent organic compoundn in
P0179tyrene.
Part 2: Determination of the molecular weight of
polymers. Vysokom.
soed. 1 no.9:1295-1266 S 159 * (MIRA 13:3)
(Styrene) (Luminescent substances)

21(4), 15(8) SOV/69-6-3-1 - '2ci
.j//
AUTHORS B3roni, Ye. Ye., Shoniya, V. M.
TITLE: Production of Plastic Scintillators (Iz~:otovieniye
--,last-
massovykh 3tsintillyatorov)
-PERIODICAL: Atomiaaya ener6iya, 1959, Vol 6, Nr 3, pj)
330-332 (USSR)
ABSTRACT On the basis of earlier experience a ner, method
ras elaborated
for the production of plastic scintillators by -means of a
thermal polymerization ir, a closed metallic container.Two
different f=s of containers were used, the cross sections
of which are available (FfgS.1p2). Theinner surface of the
mold is chromiumplated and mirror-finished. The discharge
pipe
which is so]Jered to the mold is in its pper part surrounded
by a condenser coil (made of copper) for coolin.~-: styrene
vapors and lov-boilin,, nolymezs. In order to a-,,o4d t',e
stick-
in~, of polystyrene to the walls they are rubbed with a
flannel
cloth which was steered into a lr,~' -A-ture of pure
anhydrous
[:Iycerin dis3olved in pure alcohol. '-,'he purif-ied
styrene in
vihich the luminescent admixtures are dissolved is poured
into
t'ie mold which is then hermetically closed. The still
present
nl.r 1S replaced by nitro-on. Polyziari~ation io carried out
Card 1/2 by stepwine heating up to 140 0C.' At the time
tile coolinj~

Production of Plantic Scintillators SOVIB)-6-71-1412)
water is suitched on. In the course of 2 hours an exothermic
reaction takes place. Temperature is then increased to
2000C. At this temperature polymerization is finished afler
20 hours. After the end of the polymerization process the
entire apparatus is slowly cooled down to 100 0C. ~-*.t 800C
the
scintillator is after-treated in the mold during 6 hours. The
technology described ensures homogeneous, colorless and
cavity-
free scintillators. Also in the light and in the air the
poly-
merizates are stable. An additional mechanical treatment is
not necessary. The fluorescence properties can be learned
from.
reference 3. There are 2 figures and 3 referencep, 2 of which
are Soviet.
SUBMITTED: August 19, 195B
Card 2/2

S/079/60/0,30/05/57/074
31 o 0 B005/B125
AUTHORS: Baroni, Ye, Ye., Kc-:yrzina, K. A
TITLEt On p,p'-~ah~n3~1 Stil~e~ei
PERIODICAL: Zhurnal obshchey khimii, 1960, Vol, 30, No, 5,
pp., 1670-1673
k-
TEXT: To increase the efficiency of plastic scintillators in
scintilla+-icn
counters it proved to be expedient to add two luminescing
organic compour,&-
together, One of them acts as main activatorg while the
other is only
added in small amounts and is used in the role of
co-activator for shift-
ing the fluorescence spectrum and for increasing the total
effect of the
scintillator, p,pl-Diphanyl stilbene is especially suitable
for the co-
activator (Refs, 1-5), The authors of the present report
worked out z-~
production process for this compound, Diphenyl served as
initial prodtict.,
which --.4as converted into p-diphenyl aldehyde by
carbonylation (Refs. 6,
'Phis aldehyde yields p,p'-diphenyl benzoin in the benzoin
condensation vdt-a
sodium cyanide in an alcohol solutions For steric reasons
these compounds
cannot "t~e reduced with the aid of the usual reduction
process for the
prod-action of stilbene from benzoin (Refs. 9-11), The
authors trace out
Card 1/5

On p,pl-Diphenyl Stilbene S,1079/60/030/05/57/074
B0051 B1 25
a new method for the reduction of diphenyl benzoin :Ln a
hydrogen atmoEPh!eXa
with the aid of zinc dust and concentrated hydrochloric acid.
With the
use of usual zinc dust cis diphenyl stilbene forms Jin the
form of white
crystals. When, howevor, the reduction is carried out with
amalgamated
zinc dust trans diphenyl stilbene results in the form of
greenish-yellow
shiny flakes. These two geometric isomers differ in their
fluorescences
(Refs. 13-18), The absorption band of the cis form is found in
shorter
wave lengths; also its absorption maximum has a loweir value
than that of
the trans form. Fig. 2 shows the absorption spectra of the two
geometric
isomers of the diphenyl stilbene in dioxane. Characteristic
differences
also appear in the fluorescences of the two isomeric forms in
the crystal-
line stated the trans form fluoresces intensively blue, while
the cis
form shows an essentially weaker fluorescence, violet in
color. In organic
solvents both forms fluoresce violet; the intensity of the
radiation is,
however, here also greater in the case of the trans form. The
trans form
is more effective than the cis form in its characteristic as
co-activator
-for scintilla.tors, The results of the measurements with
res-pect to thig
will be published separately. In heating in nitrobenzene the
trans form
of the diphenyl stilbene changes into the cis form. The same
effect occurs
Card 213

On p,pl--Diphenyl Stilbene S/'079/60/030/05/57/074
BC,05/BI25
also in the longer action of ultraviolet rays on crystals
of the traE:- ~ I
form. The synthesis of the two isomeric forms of the
diphenyl stilbe."e i-f
thoroughly described in the experimental section, There are
2 figures
and 24 referenc6s, 3 of which are Soviet,
SUBMITTED% May 27, 1959
Card 3/3

RkRONJ, Te.Ta.; KOVYRZINA, K.A.; ANDMISHCHU, Ye.A.
Synthesis of some A2 -pyrazoline darivativea.
Zhur.ob.khim.
30 no.6:2002-2008 Je '60. (W.HA 13:6)
(P~rrazoline)

2115 Z 00 69139
AUTHORS: _Baroni,__Ye._-Ye.j Kovyrzina, K. A., S/076
60/034/03/027/038
R 0- 2 m wn_~_~. Andreyeshchev,_Ye. Ye., BOON016
.Shoniya, V. M. (Sukhumi)
TITLE: Plastic Scintillators on a Polystyrene Basis. III
PERIODICAL: Zhurnal fizicheskoy khimii, 1960, Vol 34, Nr 3, pp
665-667 (USSR)
TEXT: The authors synthesized polystyrene scintillators with
additions of various
Jerivatives of pyrazoline, oxazole, and stilbene according to a
standard method
(cf Ref 2). The synthesis of some of these additions which have
not yet been
described in publications, and the influence exercised by the
cia-trano-configura-
tion of 1,3,4,5-tetraphanyl pyrazoline and p,pt-diphenyl stilbene
upon the in-
tensity of luminescence of the scintillators will be dealt with
in a separate
paper. The intensity of luminescence of standard samples of the
scintillators
synthesized (16 mm diameter, 10 mm height) on excitation by
P-radiation of a
Ce144 - pr144 preparation was measured photoelectrically on an
FEU-29 photo-
multiplier. Ito corrections were considered for the spectrum of
luminescence ra-
diation, for self-absorption ato. Thus, the results obtained
characterize direct-
ly the efficiency of sointillators combined with a
photomultiplier. Table 1
presents thI results obtained for the following luminescent
addtions: 22 aeriva-
tives of A -pyrazoline, 3 derivatives of 10-oxazole, I derivative
of oxazolove,
and 2 derivatives of stilbene. The efficiency of stilbenesAmixed
with p-terphenyl
Card 1/3

69139
Plastic Sointillators on a Polystyrene Basis. III S/07
60/034/03/027/038
B005YB016
was also studied. For each of the additions investigated the
table gives the con-
centration the addition of which causes maximum luminescence of
the sointillator,
furthermorep,the relative efficiency on direct excitation of the
addition by ul-
traviolet radiation, and finally the wavelength o.n whioh the
maximum of the emis-
sion spectrum is found. All these values are given vithout
corrections. The effi-
ciency of an addition is directly proportional to the qnsintum
yield In fluores-
cence and depends on the agreement between the luminescence
spectrum and the
spectral sensitivi-ty of the photomul-ti-plier. -The efficiency
of -the sci-n-tillator
further depends on the extent of excitation enorgy transfer from
the polystyrene
to the addition. Among the additions listed in table 1 there are
s'ome causing
a very high doinii1lator efficiency# which may thereforebe
recommended for the
manufacture of saintillators. The authors also investigated the
applicability of
some-of the above-mentioned additions to the shifting of the
spectrum in poly-
styrene scintillators. Table 2 shows the relative efficiency of
4 derivatives of
Z-pyrazoline and of 2 derivatives of stilbene with respect to
the shifting of
the spectrum in polystyrene saintillatorB. The measurements were
also carried
out by means of an PEU-29 photomultiplier. The concentration of
the additions in
these experiments was 0.001 g1g. There are 2 tables and 3 Soviet
references.
Card 2/3

69139
Plastic Scintillators on a Polystyrene Basis. III S/07
60/034/03/027/038
B005%3W
SUBMITTED:
May 28, 1959
Card 3/3

27700
S/12o/61/000/003/010/041
L E073/E335
0 b
AUTHORS: Baroni, Ye.Ye., Kilin, S.F., Kovyrzina, K.A.,
_iFoz-m`an__,_T_.M. and Shoniya, V.M.
TITLE: On the Duration of the Light-emission of Plastic
Scintillators
PERIODICAL: Pribory i tekhnika eksperimenta, 1961, No. 3,
pp. 72 - 74
TEXT: The results are de5cribed of measurements of the
light-emission time of the relative yield of luminescence for
a number of plastic scintillators based on nnlvstvrnne and
polyvinyltoluol. The measurements were made by means of an
.&-ray phase r-Luorimeter. The data permit estimating the
lisuitability" of plastic scintillators in"high-speed
circuits".
The measured Tluorinetric times" are tabulated for plastic
scintillators with a single luminescent addition. It was
found that the times urere particularly low for scintillators
made of di- and triphenyloxazo.10, diphenyloxodibtzole and
n-terphenyl.Of ttle investigated scintillators the largest
H/Ir,
value was obtained for scintillators with n-terphenyl, the
Card 1/4

27700
S/120/61/000/003/010/041
on the Duration of .... E073/E335
optimum concentra-ion being 4 g per 100 g of monomer. The
dependence of RI-jr, on the polymerisation conditions of
polyvinvltoluol showed an unexelained decrease in -t:~ in the
case of polymerisation at 200 C. The fluorimetric time
for polyvinyltoluol equals 13.5 nanosecs for a polymerisation
time of 120 hours at IZO 'C and 11.5 nanosec for 30 hours
polymerisation at 200 C. Spectrum mixing agents bring about
an increase in H owing to a decrease of the self-absorption
in the basic addition and lead to a better correspondence of
the emission spectra with the spectral sensitivity of the
photo-
electron multipliers. However, the value of 'I,- also
increases
simultaneously. The r0le of the spectrum-mixing agents 4P,
PPS and StS consists basically of the transformation of the
short-wave part of the illumination spectrum 3P into a proper
emission spectrum. Thereby, the influence of' reabsorption in
the 3P itself on the external magnitude of the scintillation
and on the duration of the light emission is excluded. The
obtained data show that as regards the speed of the response
(H/-Y- ) some plastics are superior to stilbene. Table 4
5hows
Card 2/4

on the Duration of
S/I 20/ 15W000/003/010/041
E073/E335
the comparative 'Values; all the plastic scintillators had
a diameter of 28 mma/height of 25 mm with a MSO reflector
and HY was measured by means of et photomultiplier VY-1.1
(FEU-29). There are 4 tables and 8 references: 5 Soviet
and 3 non-Soviet. The two English-language
quoted are: Ref. 1 - R.K. Swank,
Instrum., 1955, 26, 15; Ref.
J. Chem. Phys., 1956, 24, 670.
SUBMITTED: June 21, 1960
references
W.L. Buck - Rev. Scient.
2 - R.C. Sangster, J.W. Irvine
Card 3/4

AUTHORS. ATI-irev-:!-~hctiv~ Ye A
Mid I M.
2 96 L3
S/120/61/ )00/0011/024/034
E'202/E~92
Baroni-Y-t --- ~Lp-- Kursanova N S
TITLF- Press-moulded plaslic phosphors w, th organo-metallic
adoi tives
PERICII)ICAL: 11ribory i tekhnika eksperimento 1- ;t 1')6 1 1
',).1
TEXT. Thr, atitho! s ot)-terved the nhvTo-.!i Jr-s ()t-
lumines-
cence in scintillat~4ng phosphors vf,4i In the orthodox
way by dissolving the oi.4ano-metallic comr,(,!rrlm;
io,~.ether with the
luminescent additives iii a monomer and subsv(j-;4-nf!.v
,)olvmeri9injq
the whole mixtitre, Tns, r~~ut the authors intr(~oiic!-(i
sliccessfully
,aiv)-seatimetallic comnoiiiiii-~ into plastic
organo-metallic Avd er~r
phosphors at th#! stage of press moulding vxi~--rimonts were
based on a plastic phospboi derived from tht- im tymee-.i sat
ion of
styrene with 3A, p- terpheov.1 and 0 04% 1 3
')-tr!tlitt-iiN-4-1!-pyrazoline-
Powder mixtures 0!' LhP aurove were compounded with v.,ch of
the
following- 11WC H- ) Hy, ( '~11 -A Sn(C H ) ana if-I- and were
11 : If --, 2 6 5 it t~ " " 2
press-moulded !or 1; iGiirq at J-~9-130-C at a of 2 5 kg/Cm
in a spl i t me t a i I - c moki Id i n x he ab seiic e o L' i
no v z Since the
Card t/3

296.ti
Press-moulded pl,%-~tic po(~-4t~hors S/11!0/t)lf
E202/Eit)~-,
melting points of the L.i-i; !wo add-it.-ives were the
moulding
temperature the ihosphorn were turbid the
remainAng two ;%dd3tives z,z.~- ri%P to transparer.1L
phospnors The
luminemcence ni. itie abov(, ~):,~osphors was me~%stir,t-d
I'T-)m the mean
current off a ptio,omultipl- c (,xp(.-,%ed to t*-s and i I was
found that a ,er -, s t t w. t-nc hi nK o f Itim i n ri, 4,
cjs cit rr ed in
phosphors wit It tl-z, , .-utrjounds Thi s wft,-; 4 t z oii t
-(i to the
relatively easV torniati(-i el phenyl radicals and th,~i.r
interaction
with the agents responsibl.t- Oir luminescence On flik- other
hand.
relatively low (ju4-ncn.L1ig o! !ead and tin comp~~-,ind~.
was explained
by the absence oi ptieziNll r~-,dicals The lowes, u1 lumnes-
cence was observed with ine tin compound add--tj%-p V, I Z
5'1~91 W/w of
Sn, in the phosphor redtized the relative luiviin(-~icence
c-titput to
60%. All samples were It min thick and 36 mm in di,imf-tel-
There
are I table and 1 2 Soviet and -) The
"I as f'ollows rfe. lias I I e
j Chem Fhys (31) 1 4 . M Hyman IRE
Trans Nu c 19rib No 3 87
SUBMITTED, Sew calbes "11) i 1)b0
[Abs t rac tor s So t. e ~ Th e wr. r d "organoelemen Ea I
r!. ,,notner
Card 2/3

196i3
2
press-moulded plastic phosphors s/i2o/bl/G~)0/004/024/034
E202/E59'.--:
is more than justified to forego the semi -metal I ic
character of
As and treat the whole group as organo-metall.ir-I
A /
Card 3/3

S
AUTHOR: Baroni, Ye. Ye.
TITLE: Structure of plastic
the temperatDre depeidence
determination of the
PERIODICAL: Vysokomolekulyarnyye
52 57
S/!q0/61/00"/OO7/0O/O21
B101/kO8
scintillators. III. Investigation of
of the refractive index and
teMLerature transitions
soyedineniya, v. 3, no. 7, 196!, 956-959
TEXT: It was the purpose of the present study to obtain new
dats on the
state of the luminescent admixtures in polystyrene
scintill.a.tors by
measuring the refractive index at different temperatures.
P-lystyrene
samples were prepared by the standard method (thermal
Doly.,..L-.,z,:,Lun with-
out initiator), which contained the following lumines-:;nt
substances as
admixture (in 1,2 by weight) p-terphenyl (3r') ; p-terpheny)
(31/".) + 1 , 2
.5-
2_
triphenyl-ft pyrazoline (0.0211o); p-terphenyl (3"') 4
1,1,4,4-tetraphenyl
butadiene (O.06c'3);1,1,4,4-tC-traphenyl butadiene (3-');
2,5-diphenyl oxazole
(1.3',,'a) or anthracene (3,/,). The disklike samples (diameter
10 mm, thickness
1 0r 10 mm) were polished and the refractive index was measured
on an Abbe
refractometer, the temperature being adjusted by means of all--
-15;'(TS-15M)
Card 1/5

2,:`157 S/igo/61/003/007/001/021
Structure of plastic ... BIOI/B208
thermostat. K 2RgI4 was used as contact liquid betweaisample
and refracto-
meter prism. The following results were obtained: 1)
IndepEndent of the
concentration of the admixture a salient point appears at'
+73~50C in the
temperature curves of the refractive index (also in pure
polystyrene).
This point corresponds to the transition of the second kind
already
described by R. H. Wiley and G. M. Brauer Osee below),,,, and
is due to the
presence of low-molecular fractions. 2) A second,weaker salient
point
was observed at +900 C. It corresponds to the vitrification
temperature
in agreement with the data by Yu. S. Lipatov, V. A. Kargin, G.
L. Slonimskjy
(Zh. fiz. khimii,, 32, 13'i 19~8) and M. L. Williams (see
below). 3)
The melting point was 119-120 C, 4) the effect of the admixture
concen-
tration of the refractive index is illustrated in Fig. 2. The
refractive
index increases linearly with increasing admixture
concentration'the
most in the case of 2,5-diphenyl oxazole. This is explained by
the
specific volume of the oxygen atom of this compound. The
deviation
from linearity in 1,1,4,4-tetraplienyl butadicne is consi~iered
to be
due to copolymerization of this compound with styrene. 5) The
density
of pure polystyrene was 1.0376�0.0005, that of polystyrene with
admixture
Card 2/5

2525' S1 190/61/00 3/007/001/021
1
Structure of plastic B101/3208
was somewhat higher. 6) If pure polystyrene is polymerized at
2000C the
refractive index changes, de-pending on the time o-f
polymerization (Fig-3).
A competition between polymerization and depolymerizat;on
processes is
assumed to be the cause. All polymers with admixture.show
an,increasing
molecular weight as compared with the initial molecular weight
which was
determined immediatply after preparation (ca 70,000 - 80,000). -
There are
'3 figures ana 15 rrete:,ences: 9 Soviet-bloc and 6
non-Soviet-bloc. The
most important references to English-language publications read
as followss
i.H. U-iley, G.Y. Brauer, J. Poly=er Sci., 1, 455, 1q.jaj R.s.
Spencer,
R.F. Boyer, Appl. 'Physics, 17, 398, 1946; M.L. Williams, J. Phys.
Chemistry,
9.) 9 5 5
SUB1.11TTED: 7, 1*~160
Card 3/5

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52 56 SP ~"V6 3/007/002/021
D E
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Card 5/7,

ALEKSIJIDRIYA, SFVANGIRU)Zl,,', R.R.
Electron diffraction study of a plastic scintillator.
VysoPom.soed.
3 no.8:1285 AF '61. (MIRA 14:9)
(Scintillation counters)

ANDREYLSHCHEV., Yo.A.; B.A.RDVI, Ye.ye.;
YURSAITOW-, RNIKAJI, I.M,
Compres3ed plastic scintillators with additives of
organic
compounds of metals. Prib. i tel:h.eksp. 6 no.4:151
JI-Ag 16L.
(MIFJ, 14:9)
(Scintillation counters)

S1079J611031100210161019
B118/B208
AUTHORS: Baroni, Ye. Ye. and Kovyrzina, K. A.
2
TITLE: Formylation reaction of1d _pyrazoline derivativ:s
PERIODICAL: Zhurnal obahchey khimii, v. 31 , no. 2, 1961 ,
627-628
TEXT: There is only a limited number of methods of introducing
the aldehyde
group into heterocyclic compounds. Gattermann's reaction (Ref.
1) was Used
to some extent, but gives only poor yields and meets with
certain experimen-
tal difficulties. A direct formylation in the heterocyclic
series was first
performed by W. 1. King and F. P. Nord (Ref. 2) who used methyl
formanilide
and phosphorus oxychloride as formylating agents. In Ref. 3, A.
W. Weston
used ethyl formanilide for this purpose. 11, 1946, dimethyl
formamide has
been patented as effective agent for the formylation of
aromatic tertiary
amines (Ref. 4). F. T. Tysor. and I. T. Shaw (Ref. 5) used
dimethyl formamide,
and obtained 3-indolyl aldehyde in a 72% yield. This
formylating agent dif-
fers from methyl formanilide by its comparatively low costs and
high ef-
ficiency. In recent years, the aldehyde group could be
converted to thio-
phene (Ref. 6), to some pyrazole (Ref. 7), furan (Ref. 8),and
pyrrol deriva-
Card 1/2

S/07 61/031/002/016/019
Formylation reaction ... B11 BYB208
tives (Ref. 9) by dimethyl formamide. The authors formylated
1.5-diphenyl-
A 2-pyrazo2nepvith dimethyl formamide. The introduction of the
aldehyde
group into 2_ yrazolines offers new possibilit*es of
synthesizing luminescat
heterocyclic compounds. Direct formylation of2 2_pyrazolines
with dimethyl
formamide is of practical interest owing to simple reaction and
good yield.
Formylation is best carried out with a sixfold excess of
dimethyl formamide
at a temperature of between 95 and 1000C. Higher temperature
(125-1300C),
and reduction of the amide quantity results in lower yields and
gives
resinous products, even causes carbonization. There are 8
references:
2 Soviet-bloc and 8 non-Soviet-bloc.
SUBMITTED: February 29, 1960
Card 2/2

BARONI, Ye.Ye.; KOVYRZIRA, K.A.
Synthesis of luminescent heterocyclic compounds.
Zhur.ob.khim* 31
no.5:1641-1643 Yor 161. (MM 14:5)
(Heterocyclic compounds) (Imminescent substances,j%

5
S/844/62/000/000/107/129
D408/D307
AUTHOA: Baroni, Ye. le.
T IT LE Concerniniz; the damage of polystyrene by ionizini,
radiation
JOURCE: TrLld~' 11 VOC!3JYLAZIIO,-,'>O soveshchaniya po
radiatsionnoy khi-
.,iii. iA. by L. ")'. Polak. Moucow, L,,d-vo j~N 3";SR, 11,162,
629-033
TZXT: Tho ruactioiw occurring when. polystyrene is irradiated with
-i and 3 r7o s in thu presence of atri.ispheric oxygen were
investi-atedt
P10 144_ 1'r 144 oour-
U')ing compounds of Po ;LII(i Ut' ~;e as the ridi-ttion -
ce.s. li'o dif.-Cerence was obLerved in the behavior of pure
polystyrene
LIM! pollystyrene ,.dulterated with laiIiinLscent materials wiien
irradja-
.ed. Surface 1,iyers o.' the polymer were oxidized durinr;
irradiation,
j
'111d inside, the sample, where oxygen and moisture -aere
~Lbsent, con-
densation into thrc:e-dimensional products occurred.
P.-_-roxidus, al-
dehydes and carbcxylic acids were detected in the oxidized
portions.
Hicroscopic examination revealed the formation of cracks, along
.-Which minute gas bubbles frequently accumulated, inside the
polymer.
Card 1/~

3/844/62/000/000/1 07/12c.)
Concornin-'; the da-Maf;e D41 08/D~07
A:.' Minl:[ Of !L C7Lpillir,'~ Wbo,
mercury thread, utt-tched to i CItss ring, in th(2
Vadi,,ltion
source :,.id tulic )ulymer sample v.,ere located, was-
used to ictermine
tLe amount of oxy:,e-i zabz;orbed b:i the saml)le under
tie action of
i3 radiation. There -ire 2 figures and I table.
Card

S/120/62/000/005/036/036
E075/E436
AUTHORS: Baroni ye.Ye., Petrova, N.P.
TITLE: Zone inelting of organic compounds on a microscale
PERIODIC%L: Pribory i tekhnika eksperimenta, no-5, 1962, 198-igg
TEXT: Small quantities (1.0 to 1.5 9) of*anthranilic acid,
dipheny.1, anthracene, o-nitroto'luene, p-brom.ophenol,
benzophenone,
succinic acid, adipic acid, p-bromoaniline, anthraquinone',
thymol,
acetanilide and p-anizidine were purifi-ed by zone melting in
glass
ampules 7 to 7.5 min in diameter and 100 min length. The ampules
were 2/3 filled with the compounds and vacuum sealed. They were
passed at the rate of 0.2 or 0.4 mm/nin through a furnace
consisting
of four zoiies of heating (discs 12 mm thick) and-three
consecutively
placed cooling zones (h min thick) sepa.rate'd from the heating
zones
with asbestos. The method was applied to prepare pure substances
for the investigation of luminescent properties of additives in
plastic scintillators. There is I figure. 91
ASSOCIATION: Fiziko-teklinichoskiy institut AN GruzSSR
(Physico-technical Institute AS Georgian SSR)
SUBMITTED: January 22, 1962
Card 1/1

S106316 2/0()7/()05/()05/006
A057/A 126
'AlMiORS: Kovyrzina, K.A., Radaykina, L.A., Baroni '~e.Ye.
TITLE: Synthesis of 5-stilbenYl-10-diPhenYl- 2 -pirazoline
PERIODICAL: Zhurnal vscsoyuznogo khimlcheskogo obshchL-stva
Imeni D.I. Mendeleyeva,
v. 7, no. 5, 1962, 592 - 593
TEXT A method for the synthesis of
5-stilbenyl-l,~~-diphenyl- Z2~L-pirazoline
(II) from n-3-[I-phonylpropenone-(1)1-stilbene (I) Is
described. The investiga-
tion was carried out in order to synthesize a new
luminescent heterocyclic compound
with high efficiency as an admixture to plastic
scintillators, having a pronounced
fluorescence in the range of abo ut 4,500- . Compound (I)
is-prepared by condensa-
tion of stilbenaldehyde with acetophenone: 1.6 S
stilbenaldehyde is dissolved in
110 ml alcohol, 1.8 g acetopbenone and I ml 10% NaOll added,
the turbid solution
left to stand at room temperature for two days, and
afterwards the precipitated
(I) is filter-ad off, washed, dried, and recrystallized with
acetone. The final
product (II) is prepared by dissolving 4.2 g (I) In 700 ml
of an alcohol/benzene
mixture (6-: 1), subsequent addition of 2.1 ml freshly
distilled phenylhydrazine,
2.1 ml cone: HC1 and the condepsation is carried out at 90 -
950C during 28 h
Card 112

S/063/62/007/005/005/006
Synthesis of 5-stilbenyl-1,3-diphenyl ... A057X26
under stirring. After washing of the precipitate and
recr~stallization, (II) is
obtained with a 96% yield, showii~"g an absorption spectrum
In dioxane (c - 10-3
IWA 63,400; X
mole/1) with X 600 20,992.
Max. 3, 3
ASSOCIATIO14: Fiziko-tekhnicheskiy institut AN GruzSSR
(Phypico-Technical InstituLe
AS GruzSSR)
SUBMITTED: January 25, 1962
Card 2/2
1

L'1814242 - EWT(M) ADS , ASD -
ACCESSION NKs AT3002206 8/2941/63/001/000/0128/0131
AUTHORS; Andreyeshchev, Yee At; Barc-nif Yee Yee; Viktorova, V.
S.; Kovy*rzina,
K. -A.; Rozman, 1. M.; Shoniya, V.
.TITLF,i Excitation energy transfer in solid solutions f organic
substances. 2
f
SCURGE: Optika i spektroskopiya; sbornik statey. v. 1%
Lyu-minestsentsiya.
Moscow, Izd-vo AN SSSR, 1963, 126-131
.TOPIC TAGS: phosphorescence, donor, acceptor, induction resonance
ABSTRACTt Phosphorescent quenching of the donor energy and the
excitation energy
transfer from donor to acceptor were studied in several organic
substances. '1'he
solvents and solutes are listed. The experimentally determined
radiationless
transfer parameter pt (defining optical characteristic of the
donor and acceptor
molecules and the dielectric property of the media) was found to
be consistently
higher (about 1.8 times) than the value determined analytically
by the induction
resonance theory. Orig. art. has: 3 figures, 3 tables, and 3
formulas.
ASSDCIATION% none
Card 1/p/

L18743-6-1- EPR/EWP(J)/EFF1'C)/EWT(m)/EVS ASD Ps_h/Pc_L -h RMI
'-=SION NR: AT3002207 WWIYA Y S/2941/63/001/04PTOM Z31
ALITHORS: Andreyeshchev, Ye. A.; Baroni, Ye, Ue.; Ro7man I. M.;
Shoniya, V, M,
TITLE: Excitation energy transfer in solid solutions f organic
substances. 3
,Tnsf
SOURCE: Optika i spektroskopiya; sbornik statey. v. 1:
Lyuminestsentsiya.
Moscow, Izd-vo AN SSSR, 1963, 131-135
TOPIC TAGS: phosphorescence, donor, induction resonance
ABSTRACT: The quantum phosphorescent yield of tetraphenylbutadione in
polystyrene:
was measured as a function of diviphenyl ethyleneftoncentration. The
concentra-
tion of diviphenyl ethylene varied from 0.0089-2 g~/100gm of
polystyrene. As in
previous solid solutions investigated by the same authors (Optica i
spektroskopiya.,
Sbornik 1, 1963, str. 128) and by I. M. Rozman (Opt. i. spectr., 10,
354, 1960),
the phosphorescent quenching energy of the donor agrees fairly
closely with the
induction resonance theory but the! energy transfer parameter
deviates by a factor
of 1.8 from theoretical predictions. Orig. art. has: 5 formulas, 2
figures, and
2 tables.
Card 1

BARONI...-Ie.Ye . KOVYRZRIA, K.A,
Syntbesis of diphenyl- and terephenyldipyrazolinyls
Zhur.ob.
khim. 33 no.22563-586 F 163. iMIRA 16t2)
1. Fizlko-tekhnicheskiy institut AN Gruzinskoy SSR.
(Pyrazoline)

WONI Ye.Ye.; KOVYRZINA, K.A.
- tifl~-- - - ---- - -
Synthesis of di-e-pyrazolines. Zhur.ob.khim. 33
no.3-.959-963 Mr 163. (MIM 16:3)
(Pyrazoline)

-4
EWP(J)IFWT(I)IEWT(M)IMS--AFnCIASD--Pc-4-V~I
L 11218-63
ACCEMION NH: AP3001632 S/0192/63/004/0Q3/0439/0W
AUTHOR-' Baroni Tea, To.; KsenofoAov, V. A.: lucheElljoy, A. Ge
Oliferchuk N. L.;
Shuand;r,
TITLE4. Nuclear roAnnnnee of scintillatora based on polystyroles
SOURCE: Zhurnal strukturnoy khimii, v. 4, no. 3, 1963, 459-460
TOPIC TAGS: MR of protons., polyatyrole and plastic scintillators
AWTIZACT: rh,13 sqdy shows an experimental jetermination of some
features of NMR
in the R 1 styrol Vand plastic scintillatortrbased on polystyrole
which could be
utilizedyU_ the stydy of structural propertiese It was established
that the WR
proton spectrum'in the polystyrole and polyst1role, with added
scintillating sub-
-30C consist of two components: wide -with
stances at temperatures higher than 20
DELTA H approximately equals 6-7 gausa and the narrow with DELTI H
approximately
equals 0.35 gauss. Theamplitude'of the narrow polystyrole component
shows a tem-
-120C. With the introduction of ltumine3cent materials
perature dependence at about
the transition point is shifted into the region of lower
temperatures. The wide
component shows a transition of polystyrole at a temperature of
approximately 75
Card 1/2

L 3-121-8-63
ACCESSION NR: AP3001632.
and 12DC.' The introduction of scintillating materials shifts the
point of transi-
tion to lower taVeratures. -%A33 additions up to 3% do not affect the
tranaition
at 75C. The M method may find its usefuln63s in the determination of
a known
concentration added to the polystyrole by means of shifting the
transition points
determined from the temperature depepdonce of the amplitude of the
narrow como-
nent at the appropriate temperaturet, "The authors express their
gratitude to V. M.
Shoniya for the preparation of polystyrole and the 3cintiUatora in
its base for
these-investigations." Orig. &A. has.- I figures.
ASSWILTION: Fiziko-tekhnicheddy institut AN Gruz Ma
(Physico-Technical Institute,
Gram SM)
SUMaTM 293an62 DATE ACQ: Olaul63 ENCL: 00
SUB CODE: 00 NO REP SOV: 001 Orm: 001
Card

A-N-DRE"fMHGH!E'V, Ya.A.; BARC111, Ye,,Ye.;
VIKTOROVA, V.S.;
K.A.; RCZMAN, I.M.; S!"0111YA, V.I.',.
Chemical transformation during polymerization
inve---,tigat--d
by meLns of absorption spectra. Vysokom. soed. 5
no.10:1482-
1484 0 163. WIRA 17: 1)

'60
~;3j AFM q ~
AFED/AM/ASID
t

S1006
NRI A
9/64 0171006/449.7 OW,

S FO; dii. T.-'~'N. Ro x
A Ut THO "Barant Yim ~-Yii' Kit, bi a'

T;TLZ'$ jntr'jj~tt
0 ..."Impou [is tie

_1964' 497-
5OtJjtCj i: yAayft- ene Y ._V " - - 0
6
00

*d j j t
01_~~e r I
polys pun -
C TACO I t p cop

, j

a 1`4 U -M&tij T~ a d 8 oitk tioit cl~ui t Or

Y!-Ir* rati" r neuir6n".9hie 4 as. ~amd
'MACT,. Hater a a or

A 611 .'Counte 9.'-~hove. b
id t~-Y hl

-top

'.-,t a t rat hdnvl f j
c ,upoxymer 240M.3
L
p
b

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112h UY IAOrcury
'
d
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enyl i
j Ph
tetrap ~
arst
hen7ttin trl~ anyl
- 0

la
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we
ton
ipheny
1 1 ., :
'L

I

L
y ~71j~jje_ d t, f h
S C L a t t I I a to r9 were,.prep .Are& ii o u4 on, Into- styrene o
SUC

luminescent additives"& Pop lyMeti-,% i tio c6nd n9L
L
r,;terp~ony 0 a n
S

L
:,of I 11%
_t4aierials -containin 12% Pb--;- 6 1 33% H8, .12%. AS. _.Sn,
"

Iio~Abad in- d :W t a
i Ot. 'Se To d resul to of,measureluents, of
6

C eff t I" Ciat kio t
ency of a icon t a n, n Fb ,Hg- or 8 d 'a

2JV4 , ..t i
in Or LIg 4 .,.AT

BARONI, Ye.Ys.; KOVYRZINA, K.A.; TSVETKOVA, T.A.
pip--Diphenylatilbone, Part 3, Zhur.org.khim. I
no.3:513-515 Mr
165. (MIRA 18:4)

%IASILIYI,:VA, K.G.; V.I!.; 1~.t. , ", -? "', 1;
1.,
_ ; -
A - L - ; 1~ XT; FER , V . ~ I . ; T S K I R TY 1,
, ! ~ . G . ; i~ A., t I j N 7 (,. r.- ,
doktor khim. nauk , red.
(Analysis of boron and its inorgnnic ew-4--ounds',
AnFliz 'bora
i cgo neorgimicheskikh soodincnii. Pod red,
T'.o:,-kvt,., Atomlz~'Int, 1965. 267 p. Omlu 1q.1)

1'4A)

CAV.v,A,V.,prof. dr.; BARONIJAN,J.,dr.
Use of alpha-chymotrypsin-A "zolulase" in cataract
surgery.
Med. glasn. 13 no.5:321-325 My 159.
1. Oftalmoloska klinika Medicinskog fakulteta u
Beogradu, uprav-nik:
prof. dr. V. Gavka.
(CATARACT EXTRACTION)
(CHYMOTRYPSINS ther.)

"n; ember'of,tt
baronin o,
04
ti
(see loo t4 6n)~, _S"4101
Vol
A mdthod'-6~flm~proiving the-it
TIT
prop~)rti6b~.-"6f,.telep4one..comn
IIERIOD16A: RvLdi'telchnika :v:, -18 no-, 3,
0
TEXT:-"' - .The author, consider.6, a,lelephone co
~,--',,torted byla.fluctuating or periodic noise and
of.4noreasing its interferOnqbw-killing:propex
i a a~non-stat onary prooepi'--'ihe4 method consl
a able parame era". The,filter-
vari
-,,.mean square etror -folio'ws::the statistical px

'
6
8
8
00
/1
/

A,. method of
0
008
8
3/01
3/P05
/
/
Ol/D308'
i D2
M,

'
'
'

and-means of n
its improvamt V~Aisoussed The f ormu
as deri
ve
d

may , b6
appliod Ao white noise~.andlinterfeiences with
other.
spec

,
.
.
"tral, dis tributi on And show:Ahat~ irx:~ all oases the use of
variable

~_~',',-:'~.-,_parameters filter results. Ifi~~ better".
intelligibility of speech.'

-`Th6r6,are 2 -.
figures

Nauchno-tekhnicheskoye obbhohestvo radiotekhniki'.':

-i
el6ktrosvyb~zi im.,A. S. Popova (Scientific d'
'
"

-
'Technical','Boa
n an 0-
iety~ of Radio Engineeri d Ele -
5:

.
~.POPOV
tricaI-wCoiamunications -im. A.~ S

PED
SUBMIT
July 199 1961_~'~ initially),

, 22';:"A 02 (gfter:ie~ii_io~)
February..

..

T'6r:11OV.~MY, .5. 1.; 1 V.1`1'.X,,'.
Crystg.
C IIns5
y spect.r,-).-neti~r l.,ith stibiliz,-ien -of tile
position,
of the tanlitude of the spectrim, of ~i proportionlil
ccunter. Zav.
1- b. '~C
(ETR4 17-,'
1. Konstru'~--crskayp byuro

14(6) SOVI I Lf'.-59 -5-67126
Translation from: Referativnyy zhurnal. Elekt::,)tekhn.-1k--,
1959, N-- 5, p 47 (USSR)
AUTHOR: Baronin, V. V.
TITLE: Studying Velocity Pulsation i7i the Bottorn Layer of
flic Strea.-Ti in the
Tailwater Bed of a Hydraulic Structure That Has Energy
Dis,;-;pators in the
Form of Two Rows of Baffles
PERIODICAL: Nauchro-teklui. inforni. byal. Len-ingr.
politeklul. in-t, 1958,
Nr 1-2, pp 95-101
ABSTRACT: Experiments were condttcted in a vitrified
cor-cretc. chute. The baffles
were staggered in two rows with the head face placed at 450.
Baffle heights ard
their distance from the contracted section were varied.
'Velocities were
measured by cinema filming, using the Mi--iskiy and Fidman's
method. it was
found that the pulsation energy in the bottom layer -Is
dissipated dcovnstream
from the dissipators over a distance of 20-25 rritical depths.
The ruot-mean-
square values of longitudinal pulsatiou velocities oare as lcw
as (0. 04-0. 10) Tisr
Card 1/2

SOVI 112 -59 -5-8746
Studying Velocity Pulsation in the Bottom Layer of the Stream
in the Tailwater . . . .
at this distance, while they are as Idgh as (0. 12-0. 3) - Usr
at the dissip--tors.
The maximum bottom velocities fall off from (1-1. 6) - Usr down
to (0. 2-0. 5) -
Usr respectively. Without dissipators, maximum velocities aze
1. 5-2 times
higher. Placing the dissipators closer to the contracted
section is considerably
more efficient than placing them at the apron's end.
Bibliography: 3 items.
1.1.0.
Card 2/2

PIABC147) V. V., Ciindl(Into Tooh Scl (dirs) --
"Imestigation of the dispersion of
energy ands erosion of the river bad below the wn+,,Or
level In kydraulic structures
equipped with energy dampers in the form of 'knives' and
aprons". LoniAc;rad,
1959. 1L pp (Min '.:Jigher Educ LISP?, Lenirw
,xad Pol4rtech Inst im M. 1. milinin),
1~0 copies (IU,, 1,,,o 24, 1959, 134)

r-n -a r,
rd. 9
he:

~ . i ;
I. . 1.
, . . I

BARONINA, L#A*
Changes in the blood coagulation system of
patients with
breast cancer following radiotherapy. Vop. onk.
11 no.1-1:
31-34 165. (mm 19: 1
1. Kafedra propedevtiki vnutrennikh bolezney
(zav. - prof.
M.G. Masik) Ternopollskogo moditsinskogo
institut,% (rektor
dotsent P.Ye. Ogiy).

BARONKIN, A.K., inshener.
Tw6z,ty-mater tower for use in building repair.
Makh.otroi. 11 no.6:29
Je 154. (91-RA 7:6)
(Building machinery)

BARONXIM, V.S.
Remote control of two amplifying channols using a
single
connecting line. Vest. sivazi 20 no. 12:9-10 D 160.
(MIRA 13:12)
1. Starshty inzherier Moskovskoy gorodakoy
radiotrwislyatsionnoy
seti.
(Raclio stations) (Remote control)

BARON, S.G.; GUBENNIKOV, V.V.; LYJJBINSKP~', NJI.;
TSEYTLIN, G.D.;
BAIRDNOV, A.Ya., red.
(Easing the start of engines in winter] Oblegchenie
puska
dvigatelei v zimnee vremia. Moskva, Nauchno-tekhn.
izd-
vo Y-va -irtmobillnogo trunsporta i shosseinvkh doro
P%SFSR 1963. 70 p. ~MIRA 17:10)

S
633
.B2
Baronovj M F #ED*
Primneniye Udobreniy (Use of Fertilizers)
Moskva., Sellkhozgizj, 1958.
167 P- Illus.p tables.
(Peredovoy Opyt v Sel'skom
Khozyastveo
Bibliographical Footnotes.

BAROPOV,-0., 1Impitan-le7tenant
Navigation electricians. Voen. znan. 36 no.1:27-28
Ja ,6o.
(MIRA 12:12)
(Gyrocompass) (Nautical instruments)

BARONOV, O.J. kapitan 3 ranga
Helmsman and signalman. Voen. znan. 40
no.8:10-11 Ag 164.
(MIRA 17:11)

. . I . I .-. / ..-~ 1, . -~
. ', . , . ? , , !.~ 6.. ..

c., kapitan 2-Fo mni-a
q,j~c. top voci.. zri.,ln. - nc-1:16 Ja f(,'
. . 1~ . - 0.
( 1q: 3 )

. " ! G.
,
Complex urc, of nerial nnd lan.4 m-nimell- SUZ-VeYs
11-0- th., riirpo-es
of i 1 b.".
('111RA 18:41
O'ni;Y'ri E~eofinic-heskay- VOVOI-L-~ne I ,k.
1. TS~en,r, - .1-' ,!,

BARONOV, V.A., polkovnik meditsinekoy sluzhby
- -
Combined iesions of the nervous system in atomic
explosions. Voen.
mod. zhur. no.4:21-26 Ap 156. (MLRA 9:9)
(ATOMIC BOKB--PHYSIOLOGICAL &VACT)
(NIRVOUS SYSTIK--WOUNDS AND INMINS)

NTNOV. V.I., Dolkovnik mad. sluzhby; WONOV, VjL, T)olkovnik
med. sluzhb7;
TITOV. A.I., nolkovnik mad. sluzhb3r, dots.; IAIZOVSKIT,
Y.T., polkovnik
Tied. sluzhby; SMIRMV, K.K., )olkovnik red. sluzhby, kand.
mad. nauk;
DOV7,930KO, G.I., Dollrovnik mad. sluzhby; MUM. P.G.,
polkovnik mad.
sluzhby; GORYLISHIN. G.S.. ,)odpoD-ovrjik ned. sluzhby;
SH*C nov, N.I.
T)j)dT)o1k6*nik mad. sluz1foy; ZMK, Ye. G., wapolkovnik
mod. alushby: BUTOMO,
N.V., raydr med. sluzhby; FFOOBRAAMERSKIY, P.V., mayor mad.
slu2hby;
TMONOV, K.B., mayor mad. sluzhby
Clinical ranifeqtations in subjects exposed to prolonged
ionizing ir-
radiation. V.)en. ried. zhur. no.2:40-43 F 157 (MIRA 12-7)
(IRADIATIOIS. effects. ft
clin. manifest. in subjects exposed to prolonged ionizing
irradiation (Rae))

SHAMOV, VladWr Nikolayevich. prof.; BARONOV, Y.A.,
doktor med.nauk;
SAHOTOKIN, B.A., dotsent; GMKHTUK, V.J.#
prepodavatel';
GRIGOROVICH, K.A., prof.; ALIKSANDROV, N.H., doktor
med.nauk;
MARGORIN. Te.M., red.; RULEVA, M.S.. takhn.red.
tSurgery for injuries of the nervous system; a
practical manual]
Xhirurgiia, povrezhdanii nervnoi sistemy;
prekticheekoe ruko-
vodstvo. Leningrad, GOS.i2d-vo med.lit-r7,
Leningr.otd-nia, 1959.
479 P. (MIRA 13:5)
1. Deystvitellnyy chlen ANN SSSR (for Shamov).
(NERVOUS STSTXY--S URG XRT)

8ARONOV, V.A., polkovnik twdit-ainakoy sluzhby, prof.
Dlagno5ts of thasequelaa rf a closed aarabriiI trauma
In ailitiry
modical expertise. Voon.-raed, zhur. no.Ba44-48 164.
(MIM 180)

Antibiotics
CZECHOSLOVAKIA LDC 615.779.93-033
BAMA, K. ; BA1LNOVAj E~ ; BELOVA, V. ; WESSIUJI, E. ;
Chair of Medical Chemistry,
Medical Faculty, P.~J. Safarik University (Katedra
Lekarskej Chemie Lekarskej
Fakulty Univerzity P.J. Safarika), Kosice, Head (Veduci)
Docent Dr K. BAMNA
"Distribution of Antibiotics in Blood. V. Tetracyclines
and Erythrocytes."
Prague, Casopis Lekaru Ceskynh, Vol 105, No 27-28, 4 Jul
66, pp 726-731
Abstract [Authors' En-lish surpnary modified]z The bond of
tetracycline to
intacT, bovine erythrocytes and to isolated erythrocytes
fractions -- hemo-
globin and stroma- in vitro was investigated. Erythrocytes
have greater
affinity for oxytotracycline, followed by tetracycline,
and finally chlor-
tetracycline. The bond is established immediately and
alters during incu-
bation period. Part of the chlortetracycline and
tetracycline is irreversi-
bly bound to red blood cells; oxytotracycline is bound by
a labile bond.
Chlortetracycline and tetracycline have a great affinity
for stroma, oxy-
tetracycline has a greater affinity for hemoglobin than
for the stroma.
5 Fig., 4 Tab., 12 West., 5 East., 1 Jap. ref. (Ms. rec.
Nov. 65).
1/1

L 10986-66 Ea(n)/r/EWP(j)/EWP(b)AWA(
a)--- IJP(C) M
ACC N1h AP6000004 UR/0080/65/038/01 1/247 479
AUTHOR: Layner, L.V.; Layneir, V.I.; Baronova, Z.A.
ORG: None
TITLE: Chemical_2olishln ~knd etching of single silicon arystals
for
exposure of d1slocailons -'?
SOURCE: Zhurnal prikladnoy khimii, v.38, no.11, 1965, 2473-2479
TOPIC TAGS: crystal dislocation, silicon single crystal,
metallography
ABSTRACT: Two ternary systems were investigated in the
experiments:
HF-HNO -H20 and HF-CrO -H 0. The system HF-HN03-H,O w." used to
estab-
lish t2e optimum'reglog f3r the polishing of a sil conpingle
crystal,
.,HP-CrO H 0 f the opti
and the system or mum region for etching to expose
fj- 2
dislocations0'The e ect of concentration of Individual components
of
the HF-1-iNO3-H'O system on the quality of the polished surface
vas deter-
mined by settj ng up a triangular concentration diagram. The
diagram was
constructed with data from the study of 230 tested solutions and
is
given In the article. A Pjgure shows the dependence of the rate
of sol-
ution of silicon with an Increase In the concentration of HN03
and the
decrease In the concentration of H? with a varying amountof added
water
For exposure of dislocations, the authors studied the etching of

ACC NRs AFC3000004
chemically polished silicon in the mixture HF-OrO3-H20. These
experi-
mental data are also exhibited in the form of a triangular
diagram. It
was established that the rate of 0olution of silicon in the
optimum
regions of the system HP-HROA-HOO is approximately 100 times
greater
than in the corresponding reglAe of the system HP-OrOYH20-
Orig. art.
has: 7 figures.
SUB CODE: 07,11/ SURM DATE: 22Apr64/ ORIG REP: 001/ OTH REP:*004

LUBFNETS, I.A.; ZHUKOV, D.G.; VOINOV, S.G.;
Sl!n'L!Yk)V, A.~,.; KG'SOY, L.F.;
KALINNIKOV, Ye.s,; CHMNIYAKOV, V.L.; YAITS~'V, GOLIYOV,
ye,s,;
MYSINA, G.Ye.; Prinimli uchastiye: F7.0, FT-GOV, 7.G.;
p Y
MENISHFNIN Yo.B.; BARNOVALOV, X.A.; G.Fi.; SWA'Al"'T,
M.I.;
Y
MOLCHANIOVA, A.A.; ANISIMOVA, M.Yo,
Refini-nf, steel with synthetic ol:ig from,
Pirj!c-c%7%cit%l %rc
furnaces. Stall 25 no.3:232-2-14, mr 16". !S:4)

L 3258k~6 --F~'IT-U-) SQTR DD
ACC NR% AR5024067 SOURCE CODE: UR/0299/65/OOO/Ol6/Gool/GOO2
AUTHOR: Baronovfjk1y,,.A..G,
T112LE: Accumulation dynamics or the photosynthetid pigments in
plant
ontogenesis in relation to phosphoroug--mit-riff-on
SOURCE: Ref, zh. Biologiya, Abs. 16G5
-b-4 0 -
PW SOURCE: Tr._I=l
__Resp. nauchn. konferentaii fiziol9g9v
khimikov rast. Moldavii. mrswifi&V---kar ya I o1 ovenyas e, 39-
1964, 1 1 Ift
TOPIC TAGSt agriculture, plant physiology, photosynthesis
ABSTR.ACT: A study viae made of geminate corn hybrids: the early
VIR-25,!
L.Iie raid-ceason VIR-117 and the late VIR-156. The plants were
grovin
on loamy ground (Biological Station of the Kiyev University).
Granu-
lated superphosphate containing 20% PSO- ( an estimated 30 of pri-
mary nutrition to one hectare'~Vlas ad e8 to experimental plots.
The
green pigments were deteniiined according to Godnev, the yellow
accordinr~ to Sapozlinilcov, Throughout the vegetation period, the
leaves'---
of the experimental plants contained frorn 10 to 12% more green
and from 5 to 6,,, more yellow. During the ontogenesis process the
Card 1/2 VDQ-531~132

L 32588-66--
ACC NR, AR5024087
content of rreen and yellow pigments increased regularly untll the
L.~ C.> LI- .'
headinrr of p,-Inlcles phtane, DurIng the following phases, their
conte,-It-
gradually decreased. Under the effect of phosphorous fer'L-1M,-crs,
IL-111'.C
ratio of the green pigzaents of the plants increased in relation
'L-.o the
relloi,.,. The difference between the hybrids in pigment content is
in
direct ration to the vegetative mass and grain accumulated by the
plants. Ye. Yurina
SUB CODE: o6/ SUBIM DATLPt Aug65
Cod 2/2

BARCXIOVSKIY, Nikolay Fedorovich
Ozokerit; dobychap pererabotka i primeneniye
Z'6zocerite; eictraction,,
treatment and applicationp by2 N. F. BaranovskiZ Z-1
7 M. F. Sukharev.
Moskva, Gostoptekhizdat,, 1959-
205 P. Illus., Diagrs., Maps, Tables.
"Uteratura": P. 202-204

Nc.

BARONOWSKI, Bronislaw, ngr.inzo
Aluninim foil Cor electric engineering. Rudy i metale
7 no.6s268-271
Je 162.

BARONSKIY, A,V.
Problem concerning the determination of criterion of
economic
efficiency of electric mot---~rs for diesel
locomotives. Sborerabopo vopo
elektromekh.no.8t342-345 163.
(MIRA 1635)
(Diesel locomotives) (Electric railway motors)

!-`ivii -r- '~:nvl n or;I
Coal :-:ines anci I'ining
IWIAC. sinA'-ini- ,f u cage lift shaft at the "Savernyi :,Ia~
anak" tr-,.d. rab. 6
no. (1~)52)
9. Monthl List of I.Russian Accessions, Library of Congress,
:,-,t, - 195X, Uncl.
2

BARONSKIY, Isaak Vlacilyalrov444,; VOIA)VICII. M."",
otv. rod.; CHEKHOVSKAYA,
T.F.. red. izd-va.
vatittlation in
[Organization of hoistiW,. haulaea, drainirg jvd -
mine construction) Organizatsiia pod"ema, otkatki,
vodoctliva
i ventilataii pri stroitellstve shakht. Mosk-va.
Ugletekhizdat,
19.58. 150 P. (mra. 11:11)
(Goal mines and nining)

BA,ZONSKIY, I.q.
Mine builders march ahead. Mast. upl. 8 no.8:12 Ag
'59.
(MIRA 12:12)
l.Glavnyy inzhoner kombinata Kwbannshakhtostroy.
(Kuznetsk Basin-Mining engineering)

BAROUSHY, I.V.
Rate of mining in the Kuznetsk Basin can be
Increased. Shakht.
stroi. no.11:6-8 N 159. (mIRA 13:3)
1. Glavnyy inzhoner kombinata Kuzbassehak-htostroy.
(Kuznetsk Basin-Mining, engineering)
j
I I

BkRONSKIY, I.V., inzh.; CBEKAREV, V.A.,
ksad.tekhn.nauk
OVertical shaft sinking in the usual way-by N. M.
Pokrovskii. Reviewed by I.V.BaronAkii, V.A.Chekarev.
Shakht.stroi. 4 no-9:32-3 of cover B 160.
(MIRA 13:8)
(Shaft Ginking) "'Ombm-
(Pok.rovskii, N.M.)

FARCINSKIY~ J~V,
u
l.r;- rate of shaft Binking in the con3traction
and
lll'.4Orc,,,.n;-za-.i-,,n of Ruznetsk Basin
mines. Ugo-- no..12:2,,
r 14 -12)
25 D III.
!~,Kuznetz;k Basin. - Coal mi-es and --rdning)

GRAFOV, L.Ye., gofmyy inzh.; GORBUSHIN, V.I., V.I.;
ZAWKIN, N.Ye.;
DUD111K,G.N.;_RAT?DNSKIY, I.V.; KOSTYUKOVSKIY,
V.Ya.[deceased];
LINDENAU, N.I.; BIRYUMT,-R.A.; LISFOVETS, ~.R.;
MUFAVIYEEV,
V.P.; FESUN, V.A.; EERDYUGIN, V.A.; BEREZNYAK, M.M.;
VASILIYEV,
1e.1.; KOLLODIY, K.K.; ILICHENKO, D.F.; YALEVSKIY, D.B.;
GERASIMOV, V.P.; IVANOV, V.V.; GAVRILOV, G.V.; SUROVA,
V.A., red.
izd-va; OSVALID, E.Ya., red. izd-va; PfbDWMVSKAYA,
V.L., tekhn.
red.
[Development and improvement in the technology of coal
production]
Razvitie i sovershenstvovanie tekhniki dobychi uglia.
Moskva, Gosr
gortekhizdat, 1962. 359 P. (MIRA 16:2)
(Kuznets Basin--Coal mines and mining)

BARONSKIY, I.V.; TSAY, T.N.
The Ab",hlevo-Baidaevskaia Central Dressing Plant.
Pr=. stroi.
41 no.2:17-20 F 163. (MIRA 16:3)
1. Kombinat po shakhtno= stroitel'stva Kuznetskogo
kamennougollnogo basseyna.
(Novokumetsk-r-Ore dressing)
(Novokuznetsk-Industrial plants)

BARONSKIY, I.V.
Dast control in the newly conotructed mines of tha
"Kutbass.-
shakhtoatroi"'Combina. Vop. bort s oil. v Sib.
no,ls65-69161
(MMU 16:12)

BAROLSHY, Isaak Vladimirovich, inzh.; 'v'ATOROV,
Georgiy
'W'O:tOb'YFV, Vladizmir Illichp KJI,!, Anatoliy
Senyumvich;
LEONTIYEEV, Sergey Nikolayevich, kand. te~hn. nauk;
MJZYKANTOV, Stepan Parlrat2yevich; PROSTEMEGV,
Grigoriy
Yevgenlyevich; TSAY, Trofim Nikolayevich
(Building of mining enterprises] Stroitel'stva
r-ornyl-h prei-
priii,.tii. Moskva, Nedra, 1965. 323 P. (MIRA
1F,:10)

j~A..
E~usii~g the start of in wint.crl Cuacgolenie
ruf-'~-.
dvigatelai v zirm.,-la
v0 !-va avtc):.(;bil'no,,,,, traiispol.4&
i963. 70

I I
-~/c,
MIROV, S.A.; HAROITYAN, A.G.
Commercial use of the new method for closed
exploitation of oil
wells. Azorb. noft.khoz. 36 no.9:23-39 S 157. (MIRA
11:2)
(Petroleum engineering)