SCIENTIFIC ABSTRACT ADROVA, N.A. - ADUNTS, G.T.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R000100410001-4
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: June 5, 2000
• Sequence Number: 1
• Publication Date: December 31, 1967
• Content Type: SCIENCEAB

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TITLE,: BJ-'frzc'ui-v, 3clntillxtors f,~)r 1~,coon,'J.7,7 of
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ABSTRACT- Var'. -)US
0,:!CI! v ot i,:-,i td:,s,
s
til lat. j
cin It has been o:. -2-i t the
followl-. at,
or or. aro
ofl`-icionu:
r-,,-.LonyI + ~;.l
2. " I ,, i_' , -
J ,V Z Ole .
t;:,,-. hc.,
hon-I + C.G' L,) 0'-*-Io
te tra-ph~anylbutL"(;
5~" rac 2~
0 U,
lic
ny
i z o -bc, n zn c
ILI~ 2, 5-di ~ic., ~Io:- 0.
Card 1/2 .Pjlc, of of ;111,-!~Llc- ~-;cLnlkdil.ators bu,-.cl

Effec,Hvc Fla7,-Uic f-)r
E --i E~ n
3peci;;on (;,,.n be cbt~tim- (I
with (1, iJT:J( It,! rs b,,vc c T~ I f i
U ab I cS, a I'l V 0 f o r ,; I - CJ~ I. "n, i 'a I I
EnE;lisli and are Dutch.
A;3330CIAT!61~ : Inoltit'llito of hi `1 "he
I _. , , I V
0_3Ci01!C(J`_' )f I.; -C,' U,;,~Rl (1:
Acade:l- Of
mo1eku1-rarnj*:_h
SUB1,11TTEM: Doco.!ibcr 5, 1()5-).
AVAILABLE: Library- of Con-ress.
1. Radioactive enipsions-Racording devicqs 7. Plastic
scintillatc-s
Card 2/2 3. Plastics-Dot eminat ion

AMOVA, N.A.; KOTON, M#M.,- YWRINSKIT, F.S.
PraWation of 1, 5-dipherq1oxasolo &-xd stu,47 of Its
velati-kiAtion
officieney An plastics. lzw.AN SSSR.Otd#kh1w..nauk
no.3085-386 Mr
157. (MMIA 10:5)
I.Institut vysokomolskulyarny%h voyaclineniy AkpAsmli
nauk OBER.
(Oxacols) (Plastic, matcriale) (Scintillation minters)

,L) 'v/7
ADROTA, N.A.; KOTON, M.M,
"'w"a"Alieparing offootlye scintillation I-lastics.
Report lo.21 Preparing
1. 4-di-[2- (5-phanyloxazolyl) ]-bantam and studying 1tv
jojft%jjja,%joS
efficiency In polystyrene plastics. hy. AN SSSR Otd.
khts. muk
no.6t758-760 A 157. (NIU 10111)
1. Institut vysokosolskulyarnfth toyedineniy AN SM.
(Untens) (Styrans) (3cintillation counters)

AUTHURSt Piplevskiyp 0. V. and Adroys, , N. A.
TITLE: Study of My~rcnne Dioxide (K iesledovaniyu dickisi
ilrtsena)
PIRIODICALt 7%urral ObehAsy KhWij 1957s Vol, 27j No. 1, PP.
136-137 (U.S.S.R.)
ABSTRACT: Dzing thn derivation of monoxide by the oxidation of
rqrcene with
acetyl hydrngon peri"dde, the authors obtained a troduct
IdervVled
as Wcene dioxide. The formation of the latttr is *Vlainod as
the result of partieLl polyrAritation of myreene and the
orlitlikis-
tion of an active oxyjMn surplus. Efforts were wade to *xpla!n
the structure of mp-cons dioxide and to bewme acquainted wM
acme of its properties. Optical methDds wer) selected over t1w
chemical oaaa becauso the latter have hardly affertd any
specific
results. It was found that one of the oxide rirgs in the
syrt,one
dioxide is oriented in the same way as in myrcere *onoxId*j Q*
orientation of the Aecond oxide ring has not been deridtd.
Hjilro -
genation of myrcene dioAAs resulted in the forwation ot dihytro-
myroene dioxide. The hydrogenation was carried out In presents
of
C&rd 1/2

AUTHORSt Pigulevskiy, G. V., and Adrova, W. A.
TITM VYrconG Manoxido in the "ItribArd Spthosi* (Y4nooklol airtso6a
v *Lat#"
Grinlyara)
M.IODICALs Zhurral Obahchey Rhimlig 1957p vol 27, No 2. pp. Y75-371
(U.S.I.A.1
ABSTRACTs Data are presented on the products obtained fm the
r*zetlon af eso-
neatum lodometbyl vith aVrme w"orldo.. In ordor to wplitin the
tehnvlor
of Weene monoxide in the r1rigneM reaction, It was decided to carry
mit
the reaction with A saturated monoxido figuring it All be poesible
vn&r
those conditions to avoid the effect of the conjupted mtem or double
bonds, The monoxide was ~7dropneted in the prosonce, of platipvt
WksO,
-The oride of tatrahydrooWroene during its reaction vith maposlum
lots
mothyl yielded an unsaturated 011H22 hy&OQArbm. It was *st4kbl"�W
Oat the anomalous Gripard reaction Is not conzictod. vith the
P""wee of 4
conjugated system. The presence 6f an Isopropylidaw grwap In the
ryo-
Card 1/2 theelsed hydrocarbon was confirmed by the lnrgw amounts nf
seeton oM9'kw4
during the ozonolysis. The results of spectral *nalysijk to w%ich
the

AUTHORSt Adrova, N. A. K')tcll, M. M Parlov Pl. F
TITLEt
The Scintillation Activity cf Carbocyc"i-, at! liol.~rl

Compounds as Related to Their Ch,)-nierl Stru-,'uro
:V), i, ;I

mezhdu khimichesicia stroyaniyom karbo- I ;P.olrntoi~
1,-JAj~'

soyedineniy i ikh staintillyntsionnoy ft1Kt1-fho8t,:f

PERIODICAL:
Doklady Akademii Nauk 535R, 195', Vol. VA, ';r

(1j5SR)

ABSTRACTs
Tho
paper under review investigAtes the r*1&1W-,,ioj
:,*61-sat

chemical
structure of the e4rtocycll; &.11

compounds and their
scintillatirp ^ctlytty.

In addition to the known inoriganic I
phnarhcrr,41 a
tf:,#

organic 'phosphors' are at present boine
WIA~4ql.v
Al;

crystalline, liquid, or synthetic scint'llatorr. Anv;
t,,~. t_*

organic compounds, f luoroscence will be ft.;inl J- i~
*q

of the aromatic hydrccarbons knd Alao In a r, ~Pi

number of
hetoroeyolic co2oounds, the

Card 1/4
contain ring-shaped structures
an~

The Scintillation Activity of Carl,ocycli,, to.kl ~i~ ik.
C,W, jt~,"n nx hp-
lated to Their Chemical Struc,.uro
carbons with 4-5 c.Yclva in th(, nolel-tl'-o ~,t-! rit
double bonds, have the hiKhe~it activity. 1r. tAf serioi% of
the
oxazoles and of the ox-Aiazoler'. Which !.etv,- vAupr ~,f
scintillating activity, tile lattor 1, - ~1 'r ."Aiiiarm!'140
degree on tho nature of %he stibitituerits in *6~& 1,,) ro i.
I in, M . . "~ .
If the substituents are tho samo t !w r; 0, -- 4-IR-o1r,
derivatives (IV) are of a h1rher nctivity I ~ .4 I'v ,, 1 .1 -
z o 10 a (V ) - Al so t lie I , 1 4 4 - I, e t rattry I bti
1. a 0 1 p n o ~~ ~ V I a n ~i Y-
-terphenyl (VII) are of i hj~,h activity. ;hr al YP intprrp-
lathnship oxista also tor the hydrocar1-;,,r,-,i t!,,-Pp '~-r-
densed nuclei which differ from each other by tht, structure
of their ringap their number of coniuiataoni, Alld I?`;"
0*110tMCM
of different heterocycles (0, S. NU). Anthrnrene *,; morv *f-
fective than phenanthracene and azenaphthpnp. In the spri*a
of the dibenzyl derivatives of Nrant thiop~',Pnp nni ji)rrolo,
the oxygen-containing heterocyc1c X1 tins t!~e
Different diarylmethanes are of loqer acttivity, -ilal it;
',!;4.)ir
crystallized statr, in the molecuie of
Card 3/4 between the ber~aene rines is interrupto-1. OnIly ~
I' lho r, I, or

;V, Ir-
fll -1 "In,
Rig. F
I -, t
pi
91
poll C
IM
.4~.4
a Alt t
At
W.3 a - ! . r go
.4 7W .6
941 Im I II I u! P.
14
aa t 4"
t. .. A
6%1
13
oil i
!13
All of A i
Ell ij
Ali I
In

,~~v
TITLE, Lfficacy of tho Ocintillaticn ol CLrbo- iond
Compoundc in Plastics Otsiati Ilya. vffe', tivilot't.,
karbo- i
PERIODICAL: ILvestiya All SSSR Seriya
pr,. 41-43 (USSR)-
Receivedt karch 8, 1950
ABSTRACTt The efficacy of the scintillt.tion Gf subitituted
aY;t*',,racer;o-,.
polyphonyls, Eiryl-derivativon, of and an nwjor Ur
hetarocyclic compounds (oxyzolcn, oxydia.,01ell k- -tc.) C!".
introduction into a v:Ls
The above-i,iontioned ijubutn~icuo w,re irito t:,i,
atyrene-monomer in quantitei corroo.,undir.6 to V.oir
efficacy (1-2~v') and were with 0,"-"
oxide at a gradual rise of frc,7. "0 to 1440C
during 4-5 dayo unti, the of tran~,i-Ia r e n t U I rn
blocks which were tben 31haped into Frum t!,,e ki'l.
tained. data it was tc -Ieter-~Ine a con.ect4ot-
the chOlLiCV.1 structiire of t'-Io ~va*~).;t.w'.coc %-:id
tl~.e
Ca:E,d 1/3 officacy of thoir acintillat.1k,n. Ct 1 ~Orjf;("
Ct.r',_ ~,Lm,!u

Efficacy ol the ScintUlation of' Cnrbo- and IluturucYclic I -
C
Compounds in 11astics.
i-ossess the highest efficacy 4n )I.-uAics: 1,i*,-di-[2-(5-
-plienyloxazolyl)] benzene (1) which io dozi,-nated 013 KICT,
quaterphe nyl ( II) , and 9- 10- di !ion-, 1 a-.-. tlXac onp
V
coinpounds with 4-5 cycles in the ;.olecule and co!lj-,;j ate
double bonds. In the series of oxazoles (IV) and
(V) with the same substituents (e.,-. phe.Vl-i-reu1,13) the
oxazole-derivatives have a higher ocintillation-act'I'vi%,
than the oxydiazole-deriv,-,tive3. 1,1'
(VI), where a - H, CH 3 and p-terphenyll (VII) also losE;ess a
sufficiently high scintillatit;n-activity. Other cc! Iounda
with 3 cycles in the molecule (authracene, r:henanthreno
acenaphthene, dibenzofuran, dibenzotliiophene' and othersi do
not ahow a high sointillation-efficacy in plautics. ~tillocnv
and tulane which in Lionucrystal-form ~ossusa a hig-h
nc-Aij,.till-
ation-efficacy are ineffective on introduction. into
1,4-diplienylbutadiene is little effective in 1,lastics,
although it possess suf"f"iciciA (.Affectivenes2 in
1101-Ittik-no.
For increasing the scintiII-Aion-efficacy of plastice it in
expedient to introduce two orranic ocintillator3 -JI'MAIlt,11-
cously into poly3tyrone. One of thoset the chcarer and cusivr
Card 2/3 one to obtain (terplionyl, dil-I"Onyloxaii0e) Ilays
t-.,e I?a,t of

Efficacy of the Scintillation of Carbc- and lleturouyclic 48-
1 -912C,
Compounds in Plastics.
a coactivator (quaterphenyl, POPOP) and is i,.,.rc,ducod iii.
small quantities but at the same tiiic it considerably in-
creases tho total scintillation-effiz;zicy of thu 1,lautic. On
the basis of the obtained exj-!rimental data t%c autncrs iro-
duced effective scilitillation-pla,3ticG on a 11...%one-base
ef a
diameter of from 30 to 150 mm and of u woir~ht up to 3 ',-C.
The
effectiveness varies from an order Of :,-.:Lj,%1'tude Of
~15," in t'le
stilbone-crystals to 50rio' in the
There are I table and 4 referviices, 2 of w'oiich are 51triic.
ASSOCT-ANON: Institute for High-MolGoular Compounds Ali
U3,;111 'Injtitut
vysol:omolekulyarnykli soyedineniy Itkadenii nauk
AVAILABIE: Library of ConeresB
1. Plastics 2. Cyclic compound3 3. Polymerization
CF-rd 3/3

24-4), 5(3) S OV/51 -7 -1 - -5/2
AUTHORSt Panov, Yu.N., Adrova nd Kotan, M.M.
TITLEs Optical Proportiez of Compoundt of the Oxatole,
Oxydlatc]G and Furan
Seriss (Optichaskiye, kharaktoristilci soyediueniy ryadov
o1ciatola,
oksidiazola I furans)
PERI CID I GAL iOptika I spoirtroskopiya, 191,9, Vol 7, 'Kr 1.
pp 29-34 (U33R)
ABSTPUTs The paper was presented at the .3econd Conference, for
Coordination
of Work on Applicatien and FroIxtration of Scintillatora. which
"a!,
hold in Kharlkov In Ncveiaber, 19C,7- To find the relationship
betwern
UL&, ohemi.eal strueturo and seintilAtion properties of orranie
vampound-i
the authors stidled optical proparties of benzene solutions of
2,5-11aryl
derivatives of oxazolec, oxydiazole3 and Puran. For this purpose
the
following compounds were synthesized and wbidied:
2,5-diphenyl-1,3-oxazo16 IPPO);
2-IL-nar,hthyl-,r-phanyl-I.,~-.~xa tole kNPO);
2-0-styryl-5-phanyl-1,3-~-xatole (SPO);
1-phenyl-5-(4-b1phanyl) -1 7-oxazole (PBO);
2-ct-furyl-5-p)ienyl-1,3-czca-.ole (FrO),
Ca rd 1/4

SOV/51-7 -1-5/27
Optical Properties of Gompounds Of the 0XAro1*, Oxydiazols and
Furan Series
tntal abo orption, of the excitation energy. The quantum
Vields of all
the compounas were extrapolated approximately to "a condition$
of
infinite dilution.. The scintillation light yields (1.9. the
maximum
scintillation amplitudes) were dotex-mined by the method
described
earlier by Adrova ot al. (Rot 6). The absorption and
luminescence maxima.
the quantum and light yields are listed fbr none of the
oxa&oles in
Table 1 (this table includes also data on torphonyl and
anthracone). The
same properties of several oxydiazoles are listed in Table 2.
The
absorption and lumlaasconce spectra of some oxazoloa and
oxydiazoles are
shown in Figs 1-4- It was found that In the oxazole and
oxydiazole cories
the luminesconce quantum yield decreased and the absorption and
luminescence spectra were displaced towards longer wavelengths
on
decrease of the number of hotero-atoms of nitrogen (Tables 3
&nd 4). In
each series the spectra were displaced toward3 longmr
vqvalengthe and
Ca rd 3/4

SOV/61-7-1-5/27
Optical Propertiew of Compounds of the Oxazole, oxydiazola and
Furan Series
the luminesconce quantum yield fell
atyryl radicals. Acknovledgment is
her help in this vork. There are 4
4 of ahich are Soviet and 2 English.
on transition from phenyl to
made to Yo.V. Anufriyeva for
figures, 4 tables and 6 references,
SUBMTTEDs August 2, 1958
Card 4/4

24(4)
S OV/51 -7-1-24/27
AUTHORS% Adrova, N.A., Androyev, V.N., Roton, Panov, Yt;.N, and
Musalev, N.S
TITLE optical and Scintillation Properties of the
Oxydiatole-Series Compounds
(Optichaskiye i staintillyatsionnyYu khmrt;Attiristik.-I
soyodinaniy ryada
obidiazola)
FERIODICAL:Optika i spektroakoplya, 1959, Vol 7, Kr 1, pp
128-1249 (TJ33R)
ABSTRACTt The authors studied plastic scintillators with
(I) 2-ot-naphthyl-5-(n-biphonyl)-1,3,4-oxydiazols (abbreviated
to uL-IBD)
and (II) 2-phanyl-5-(n-binhonyl)-1,3,4-oxydiaeol.o (PED). Their
properties
were compared with earlibr results (Ref 1) oj~ (1.-II;
2,5-diphenyloxydiazole
(PFD) and (IV) n-terphanyl. Compounds I and 11 waro prepared as
described earlier (Ref 2). Plastic saintillaIx-s .,;are prepared
by low-
temperature polymerization. The scintillatior, +utatum. yield van
daternined using apparatus described earlier (Rtf 4). For the
purpose
of th-3se messursnents the scintillation yisid of ;' 3&mple
containing 2%
by weight of terphanyl in polyatirene -m.F. Vice~i to be 100%.
Scintillatioan
were excited with y-rays from Co 0. fho abiorntionspeutmof
compounds I
and II (Figs la, 2a) were rocordod usint; a a 'ju--trophotometer
SF-4.
Fig 3a nhon the absorption E -,-,3ctr-x,,i of "F0. 'Ziis
1walneacence spectra
of compounde I and IT (Fibs lb Ind 1'rrD o1A.1ined by ineans of a
Card 1/2

3
'OV131
Optical and Scintillation PropertioF of the Oxyd ari 6.1 Ompounds
quartz monochrcmator and a photoinultip)tsr M-19; they were
excited
with light of 313 m1i wavelength. FIG 5b shows the luminescence
spectrum
of PPD. The quantum yields of luminesceinca ivs.ra datemined,
relative
to the yield of a 1 iar/=3 solution ef --.r,t1iracE)ao in
benzene; these
quantum yields wore extrapolated to inf ln~4 to dilixti ons . The
rosi!lte are
summarized in a tible on p 129. This snows that tho scintillation
yields of sVM3D and PRD art) considarlLbly hi,-her 9. ,
~jl'4.; thanthe scintillation
yield of n-tarphonyl. Reasons for thiz, ~iacuased briefly. There
are 3 figures, 1 -utblo and 1 references, of vinich are Soviet and
1 English.
GUEMITTED: January .30, 1959
Ca rd 2/2

81564
010r,
S/19 6
157 a ~13 P0 2 0 041~' 6 6
AUTHORS: Adroval N. A., Kotonz M. M.
A
TITLE: Synthesis and Polymerizationlof 3-Vinyl-295-Dipheiql
F'uran'l
PERIODICAL: Vyaokoinolokulyarnyye soyedineniya, 1960, Vol, 2,
No. 3,
PP. 408-410
TEXT: As was previously shown by onct of the authors (Ref. 1),
many
vinyl derivatives of the furan serien have a high softening
point and
good dielectric properties. It was the purpose of the present
paper to
continue the investigation of the influence exercised by the
accumulati-n
of a number of cyclic groups in thu vinyl furan molecule upon
the
polymerizability and some properties of polymers. First,
3-viayl-2,5-dl'-
phenyl furan was synthesized, and its polymerizability
investigated. As
starting material for the synthesis of 3-vinyl-2,5-diphenyl
furan the
authors used 2,5-diphenyl furan which is obtained by reduction
of tran-i-
dibenzoyl ethylene with stannous dichloride in a mixture of
hydrochloric
acid and acetic acid under simultaneous cyclization (Ref. 2).
The
Card 1/3

Synthesis and Polymerization of S/190/60/00
3-Vinyl-2t5-Diphenyl Furan B020./BoU
content of active hydrogen in the intermediate
methyl-(2,5-diphenyl-fui,.~-J.)
carbinol was determined according to Tserevitinov. The
polymerization and
copolymerization of 3-vinyl-2,5-diphenyl furan was
investigated in bulk
and solution in the presence of 0-5 mole% benzoyl peroxide and
azo-
isobutyric acid dinitrile in the temperature range 60-1200.
The resultant
p2lymeralhad a specific viscosity (n) of 0.91 and a thermal
stability
(accorTi~g to "6TT(IFP)) of 175 - 1820, while the copolymer of
3-vinyl-
295-d,Jkpheryl furan with styrene (in the ratio 1:1) had a
specific
viscosity of 0.9 and a thermal stability of 1260 (according to
IFP)~
Fig. 1 graphically illustrates the polymerization kinetics of
3-vinyl-
-295-diphenyl furan (1 M solution in toluene) in the presence
of
0-5 moles benzoyl peroxideq and Fig. 2 shows log k as a
function of 1/T
for 3-vinyl-2,5-diphenyl furan. A comparison between the
polymerization
rates of the vinyl derivatives of the furan series (1 M
solution in
toluene) in the presence of 0.5 mole% benzoy! peroxide at 1000
(Fig. 3)
kihows that accumulation of benzenr rings in the monomer
molecule uauses
a considerable increase of the polym(:rization rate. The
presence of
benzene rings in the 2,5-Position in the molecule of polyvinyl
furan
Card 2/3

81584
Synthesis and Polymerization of S/19
3-Vinyl-295-Diphenyl Furan B020.YV066
also effects a considerable iacrease of the softening point
of the
polymer. There are 3 figures and 2 regerences; I Soviet and
I US. W/
ASSOCIATION: Institut vysokomolokulyarnykh soyedineniy AN
SSSR
(Institute of High-molecular Compounds AS USSR)
SUBMITTEDi December 14v 1950,
Card 3/3

251,67 - S119 61/003/007/011/021
j31b2%220
AUTHORS: AdTova, V. A Koton, 14. M. Klhgea, V. Jh.
TITLE: Synthesis of now organotin oompuunds
PERIODICAL: Vysokomolekulyarniye soyedingniyal v* Y,' nos 7t 19611.
1041-1043
TEXT: The present paper is based on studies by J..'Curry, K.Kojima,
E.Pear (bee below) with regard to the synthesis of.compounde wi-'ah
direct
si-CH2 or Sn-CH 2 bond it the chain effected by the migration of the
H,
atom from thi disubstituted silane (OZ- stannane) to the double bold
of.'
the hydrocarbon. The authors studied this reactior. on the interaction
of diphenyl or di-n-butyl stannane with di-isorpropenyl benzene, The
following equation was obtained for this reaotion:
R
C113 CH
Pard 113

2~267 S/190/61/003/007/011/021
Synthesis of new organotin compoun s B102/B220
and infusible R.SnO compounds resultedo -There are 1 table
and 8
references: 2 Soviet-bloc and 6 non-Soviet-bloc. Tile 3 most
important
references to Eng3ish-language publications read as follows.
'T. Curry,
G. Harrison, J.org. Chem., Z1, 1219, 195B,-, K. Kojima, Bull.
Chem. Soc.
Japan, 31, 663, 1958; E. Pear, J. Polymer Sci., 40, 273,
19,59.
ASSOCIATION: Institut vysokomolekulyarnykh soyedineniy AN
SSSR (Institute
of High-molecular Compounds, AS USSP)
SUBMITTED: October 1. 106o
Card 3/3

S/190/61/003/010/010/019
blo B124 B110
AUTHORS3 Adrova, N. A., Prokhorova, L. K.
TITLEs Synthesis and polymerization of trityl methacrylate
PERIODICALs Vysokomolekulyarnyye soyedineniya, v. 3, no~
10, 1961,
15C9 - 1510
TEXTt Trityl methacrylate was synthesized by reaction
between trityl
chloride and silver methacrylate (C6H5)3 CCI 4 CH2gw--
C(CH3)COOA.g il
I H ) + AgC1 for several hours at room temperature and in
MZ-*H3)"OOC(C6 5 3
etheric solution under intensive mixing. The product
obtained was
purified by recrystallizing from anhydrous petroleum
ether. It was a
colorless, crystalline substanue having its melting point
at 101 - 1030C.
The yield was 75%6. Trity) methaorylate is easily soluble
in benzene,
methanol, and other organic solvents; it is decomposed by
water with
formation of triphenyl carbinol (melting point 159 -
1610C). The polymers
of trityl methacrylate were synthesized both by
polymerization in cyclo-
hexanol solution in the presence of azoisobutyric acid
dinitrile with a
Card 1/3

28181
S/190/61/00~/010/010/019
Synthesis and polymerization... B124/B11O
stepwise temperature rise from 60 to 1200C within 144 hr
and by block
polymerization in the presence of tart-butyl peroxide
with a atepwise
temperature rise from 120 to 1800C within 144 hr. The
polymers obtained
were insoluble in most of the ordinary organic solvents,
The resistance
to heat was 140 - 1550C (14~9(IPP)). The 1css in weight
by 3-hr heating
up to 2000C was 45%. Copolymers of trityl methacrylate
with styrene and
methyl methacrylate in the ratio 10 were synthesized
under the same
conditions. Under heating, the resulting copolymers were
soluble in
benzene and precipitated by methyl alcohol. The
polymerizability of
trityl methaery3ate was dilatometrically determined in
the block in the
presence of 0-5 moles tert-butyl peroxide at 115, 120,
and 1250C by means
of polymerization kinetics (Fig. 1'). The
polymerization-activation
eneTgy of trityl methacrylate was determined from the
tangent of the
angle of inclination of the straight li'.,e -lnk~f(I/T)
and found to be
equal to 20 kcal/mole. The factor of the exponential
function was
7 -,2
3.43-10 C-M . There are 2 figures and 3 non-Soviet
references.
ASSOCIATION4 Institut vysokomol.ekulyarnykh soyedineniy
AN SSSR
(Institute of High-molecular Compounds AS USSR)
Card 2/3

IROV
IADR Lr-IlvA-v; KHOICNKOVAI K.K.
Synthesis of some derivatives of p-vinylbenzoic acid.
Zhur.cb.klitm.
32 no.7:2267,.2268 Jl 162. (KMA 15:7)
1. Institut vysokomolakulyarnykh sordineniy AN SM.
(J~enzoie acid

ADROVA W.A.j KOTON, M.M.; MOSXVINA, Ye.M.
,Synthdais and ploymerAzation-of sam) new derivatived
or biphemyl.
Izv. " SSSR.Otd.khim.nauk;&04$.18'Y,180'7 0 162. (KUU
15:i0)
1. Institut vyaokomolek-ulyarnykh soyedineniy AN SSSR.
(Butadiene) (Polymerization)

ACCESSION NR: A?007960
S/0190/63/005/012/1817/i618
AUTHORS: Adrova) N. A.; Koton, M. M.; Uages,, V. A.
TITLE: Synthesis of organometallic polymors with 4%in atoms
in the basic chain.
SOUICE: Vy*sokomolokulyarnMe soyedineniya, v. 5, no. 12,
1963; 1817-1818
TOKC TAGS: polymer, organometallic polyn!er, organotin
polymer, organotin,
coV,ound synthesis, tin. dihydrodibutyl-, polymer structure,
polymer property,
methacrylic acid, tin. di1Wdrodipherjyl-., eti-VIene
g~ycol,methacrylie acid diester
ABSMOT: A ne-4 tin-organic polpaer has boan s3mthesized from
the reaction of
R2SrLq2 with dimethacrylate ethylene glycol and with
dimethacrylate hydroquinone.
The structurecof the compoundwe represented by
C112C11COO-2f CCOCHC112Sn-
CHSCHCOOCUSC1150COCHCH, n
w 119*, C,H,,.
=.Cj (118
Card 1/2

ACCFS$ION NR: APL,007930
The reactions were carried out in toluene, wJ th and without
initiators umer
atmospheric nitrogen, increasing the tem~perature gradually from
80 to 100-120C.
The mAecular weights were determined using the aryosoopic
4eoludque in benzol.
Orig. art. has: 14 formulas and 1 table.,
ASSOCIATION: Institut vy*sokomole1ca1yarny*kh soyedineMv AN SSSR
(Institute of
H
I
i-h-Ylolecular-44eight Compounds AN SSSR)
SUBMITTED: 26Apr6? DATE AGQ: 20Jan64 B14CL 1 00
SUB CODE: CH.. M&
NO RFY SOV: 001
- OTHER: 000
Card 2/2

A M.M.; KLAGES. V.A.
.DROVA N.A.; KOTON,
Preparation of organometallic polymers
cortaining tin
atoms in the main chain, Vysokom. soed. 5
no.12:1817-
1818 D '63. (MIRA 17:1)
1. Institut vysokomolekulyarnykh soyedineniy AN
SSSR.

A
~'ACCHSSXOH MR: AT4033976
VIAOvevat" LKe
AWN014 #AM&* N. Lek-Kou"114. ill
f potyna,-.
:TITIZ: Preparation o
:and pbosphorue &too* in the pi t',~o,
SOURCE: Gaterotsepuy*ye vy -a
macromolecular compounds);~
polyucrivatiow
'TOPIC TAGS
metallic polymer
ABSTRIACT: Mw mutallft~ pm~ 1./
T
pbeisylenatripbowletiblAss
and organnotallis "lot
in vUch He to Ong 8b or Tj It &ot C.- 1v -.A~-v'ktji %xi 9
cud '1121
ADROVA N.A.; KHOMENKC- K.T-, DTIWOW, A.-.,.
Synthesis of rpw dr-r~,O- 01,
ob, khim. 34 no. -5 -., -, 5
L. Institut vysckomolel, Lyarn3i--,'.

ACCESSION NR: AT4020708 S/0000/63/000/000/0195/0197
AUTHOR: Koton, M. M.; Adrova,_-N. Khomenkova, K. K.
TITLE, Polymerization of some derivatives ef p-vinylbenzoic acid
SOURCE: Karbotsepnyicye vy*sokomoIeku)yarny*ye soyedinenlya
(Carbon-chain macro-
molecular compounds); sbornik statey. Moscow, Ixd-vo AN SSSR,
1963, 195-197
TOPIC TAGS; polymerization, vln~lbenzoic'acid, vinylbenzoate,
viny)benzamide,
polymer physical property, polyvinylbenzoate, dilatometry,
azodiisobutyronitrile,
butyl peroxide, block polymerization
ABSTRACT: Using a dilatometric method, the a*uthors compared the
block and liquid-.
phase polymerization rates of p-vinylbenzoic acid, its methyl and
amyl esters,
p-vinylbenzamide and its N-methyl, N,N-dimethyl and N-amyl
derivatives, using
0.2 mol.% tert.-butyl peroxide or azodiisobutyronitrile as the
initiators, respec-
tively, at lXO-18OC. Some of the physical properties (thermal
stability, solu-
bility, weight loss during heating) of the polymers obtained were
also studied.
The polymerization rate*of the derivatives of p-vihylbenzoic acid
decreased in
the following order: acid> amides esters. It was found that the
polymerized
amides of p-vinylbenzoic acid have a higher softening poinL and a
higher thermal
conability than the corresponding polymerized esters. OrIg. art.
has: I figure

ACCESSION NR: AT4020708
and I table.
ASSOCIATION: Institut vy*sokomolekulyarn)fth soyedineniy AN*SSSR
(institute
of Macromolecula.r Compounds, AN SSSR)
SUBMITTED: 18Jun62 DATE ACQ: 2OMar64 ENCL: 00'
SUB CODE: OC NO REF SOV; 002 OTHER: 004
Card 2/2

CC TOM T4049864 S/ODOO/64/000/'JDO/0257/0259
Ome
ij~7
CIt
_v
i, j
y6-09by v4 VM6 afffya-Wl or cc
of pOymers); Bboinlk atnicy. Moscow, ftd-vo NnWca, 1964, 257-269
?
r
ibyll
ny mg
_2'
WAM 0. ainifta on*-vo pn"~~Mwnlity
AI VM I % CT: 'Undcar renux iii tcLr.,h%-jro,urar, fio;u*,iD-,, pniv-p-
mylben7cyl ch)orlde, pre-
jxarcd by PDIY filer I YbI_% We 11' a am I JDVC with 0. 02moll. '
azodleolnityronitrile, gave
!Q
Y Zte vl~vh dry metliinncl, and
ool rntiric ~n v I n N, V) g:n~z r
l
u; L---ic mpriovIould by
.4ca"lination.. YIzIds from-1-grpo -vInyIhcnzqyI_chIorId,_ anti 6-ml
ano Me Ah
N.
NOW 0.0~~
16
-y-I to by pol)
n S0;pTCP_2'.'_' .0000 werizing the
or apbroxilwatt
Irwn "me i e klyr ~h g at 2-80-300C In argc n under 8-10 mm Hg pressure, a
4; d

Yellow pojpn~er w1th ln~rieaaed thermal stabIlity. 7bia polymer waa
inBoluble In "ordinw7l'
solve nts,'wid Its propeTides are aBcTibei~ to Itc; rmrR7nv.r-T
a:!(!
ASSOCIATION: InsUbu vy*&okomo1ek-iL1yarry'kh s.)yedinerity AN Sc~SR
(Institute of Higl:
Po)Yrrlers, AN SSSR)
,SUBMMED- VDJun63 ENCL: 00 SUM CODE: OC
NOREF 90V- u03 OTHER. 003

ACCESSION Wfl S/01j-9WW W-010
M. M.
A
nof nov Vol
the -backbona
Rai d1nou 174, V. 6. no 6 X
TA
I top
polycandenuation, th
.ABSIRACT- Pc1Ivmer& with ben7imlda2oline Uroups in the backbona have
bt-
heen synthesize-d by Polycondeni; a t i c"', 40
phenyltetram nF-,,*itb terzpbtbaldehXd ncetalls,
a acety dIpb n7llmethane,or bixf-acetylphenyl)ether as follows'
11H
Card 1/2

L
'ACCESSION 11 R:: AP40437438
R'- CH -:1) 1 Z
c 406 cip
- 'A :-Psp~~ ~,MeTsIaTa InSOIU~Ie and intwill j6
c 3-s 1, ,..: _-.~ -
sit
p t f U I T' f r n n e~ i T15 ',: 3T -!Dn ft r"-a
m to d, c e I r- I e a
,1.-) at 400C., end ri-,. Prt. has
l tal)le.
r,i v *ki qoved',.eniv AT; %SSV
1
Ali; T, 17
,SUBMITT&Js 04uczbJ & ---- . - 0 1,11-1 -, 00
< i! Tt rn T)R cc. oc Nn Rzr sov 002 OTHE R 005
ra

ACCESSION NAt AP4045096
_ic, r on. c,.q -
po W"7-~P-o
14*
.- ------- ---- - --
Nil NH
N-
NH
tan t'
-rings --in.
4--b-a' iikbbiae _-9:tructure~-cn--the: t-he a ta-
e a a r P-rov
B-0-B units ever prepared. The polymers are n U-161 ' a--
powders solubje in sulfurle acid., Both. polymere have low molecular
weight, aiid batnt espacial!y 11, art stable In air at:300--400C.
Pclymgr T1 hvdrolyzes t n. motat aiT. Orig. art. hadl 2 fornulao,
I table,. and 1 figure,
Card 213

Z:, AS-qD C I AT TON -'In lut its
naiik SSSR Orstitute of Academy of
Sciences SSSR)
-TD -p3mg:51 EN U 1 00
SURNITTI-DI 04148VIA A
VuA .--Coljg -HT
Card 3 3

: '0" 5-j- hours k V. Vw - - - - ~ - - . -
I deteridned in 0.1-0.2,15 N solutions of foraic acj-,i, aLq Lac "- - -
- - -
det.,3rmined by heating ror one hcur wRib at '400, 400 and RkV In a.Lr.
The poly- f
conJensation occurs acccrdi~ to the rosetion
-010 ,-

NH
NI
P4
b6
plt
WR 117
W. FROM 3 448
"it 141:i
Uw=
i Z.

c.
100992-6
gation-~-and modulus of %!lasticity- at various temperatures. The
-data. are, given in
graphic form.- On the buis of the data, optimum conditions for film
d4ing' and
orientation stretching were selected. The results showed that the
polymer,is suitable
for producing high-grade polMr films, In addition to good strength,
elasticity,
and thermal-stability, the-films.also nowed good dielectric propertie /
Film me-
chanical strength could be considerably increased by orientation stret
ng in the
softened state; tensile strength attained 5000 kg/cm2 while film
elacticity and flex-
Ibility met the mat stringent specifications fSic). The polymer wan
considered t07'
be of considerable interest a-qa material for film suitable for
canstruction,'elec-_~
trical And, thermal insulationbourposes and for fibers suitable for
long-timeservice
at temperatures up to 200C. Orig.' art. has: 9 figures and 1 formula,:
.,[Bmj
ASSOCIATION.4 none
"ENCL: 00 SUB CODE:
SUBMITTED: ',00 0C 6V
ATD PPXSE;.,
'NO'REF SO: ---OD6- OT8R. 002 4068

]XILDTIEV, A.G#; ADROVA, N.A.; BES-SONOV, M.1,# XOTON,
M.M.- KUVSIITNSKLY, Ye.V.;
WIJDAKC,V-, MMISTUY, F.S, I y
Electron paramagnetic re:ivnaime atady of free ra6lcals
In polyimides.
Dokl. Ali O"ISR 163 no,51ii43-12.46 Ag 16.5,
(MIRA. 18~38)
1. institut vyFokomo1ekuJyarn5rkh a0yedinc-nay AN SSSR.
2. Chlen-
kcrrespmdan-t Ail SSSR (for Eoton),

ADROVA, N.A.; KOPOI,,', M.Y.; VMSYVM, -Ife.1116
Syntherin of r,.-w aromatic Pv]~Lmldes based on
313:4,41-diphenyltetracarboxylir,, acid
dianhydride. Dokl.
Ali SSSR 365 no.5tlO69-1070 D 165. (MIRA 19:3-)
2. histitut vysokomolekalyarnykh sayadineniy AN
S~SSR.
2. Chlen-korresponderit All SSSR (for Koton).
Siihmitted
April 34# 1965.

t 01263~67 EwT(mWr f-jvTe-Y-w/'ftX----,---
ACC NR% APW03490 W SOURCE CODE: UR/0020/66/166/0010100~l-/009-4,
AUTHOR: Adrova., N,, A,;
Koton, M. M. (Corresinnding mmber AN SM); Prokhr. rova,
ORG: Institute of Hi.0-1~bleciular-Wsight Com~ounda, AN SM
(Institut vysokomolekul-
yarnykh7oyMinen AN SSSR)
TITU: Synthesis of themsD-'r -Menzir4dazoles wi,,~-, oxide and
~J- 4. pALny1_
dipheqylsuMne links in th z-.rn chal-,
-4
SOURCE: AN SMA. DDklady, i66 re.) '1966; 91-9,14
TOPIC TAGSt organio synthetic prooesoj, resin., th6rm&1 stability
ABSTRACT: Pblybenzimidazoles were synth9si2ed by thermal method
(at 3000 ir arff.)n
a tmospherewith subsequent heating in vacuo) according to the
scheme;
4,160CO_//~_X_// \_COOC
li:N-( ~113-Nll:+,r
H N- Nil
Nil Nil X-4
N XM N
where X -0-, -SG2--.
Card 1h -5-4

ACC NR. W7001410 A/) ---S--O-URCH CODE:
UR/0413/66/000/021/0110/yIll
INVENTOR: Koton, M. M.; Adrova, N. A.; Dubnova, A. M.; Bessonov,
M. I.;
Rudakov, A. P. -W ------
ORq: none
TITLE: Preparative method for polyimides. Class 39, No. 188005
[announced by the
Institute of Yfacromolecular 6mpounds AN SSSR (Institut
vysokomolekulyarnykh
soyedineniy AN SSSR))
SOURCE; Izobreteniya, promyshlennyye obraztsy, tovarnyye znaki,
no. 21, 1966,
110-111
TOPIC TAGS: polyimido_,,el sticity
ABST,RACT: An 'Author Certificate has been-issued for a
preparative method for polyi-
mides, involvina the polycoadensation of pyromellitic anhydride
and an aromatic
diamine. To produce poly:'%Mi(,es exhibiting high elasticity,
hydroquinon.e bis(4-amino-
phenyl) ether is used as the! ainine. [SM)
SUB CODE: 07, ll/ SUBM DATE: 07Jun65/' ATD PRESS: 5109

kj~q. NRI jP Wj
UW5190/ WiT662707075eei,
-APTH _r nk
Fro
Shiba % A. .-A hivi 0111 $01sel jMes Lo-Ail
" .NJ
Adrova, Nat AO:7
ORGI Insti-t4te of H&h-Moieciilar PpjLmrsi~ AN SWR (Institut
7yookamolskulyarnykh
Isoyodineniy AN &5M),
TIThEt Cryst ty -of--p tame nzimidazoU
4nd qly-2iV-od thrlenv-5*91-dibe imidazoU -7
-SDURCEs Vyaokonolaku),varft)7o-sovWineniyaj Y# Up no# 2p 1966p ?78-281
~IWIC- TAGSt--.x- dif olymer/-IIR
ray!, fraction study) crystalline p X-ray -diffroaction-
j-_50?
aPP2
ABMAQTi~ X-.~ray diffraction study of..Vreshly prepared fib r and filMj
of poly'-2s2ft-
octametWene!*>',50-dibenzinddazole (1) disclosed a
crys-tallAne'structure of high
in spite, of',earlier observations to the cont
order for that, polymer., rary by the
authors as-wall an by other workers_(A.'A.:Izyn9yevj V. V. Kurashey, V,,
Vo Korshakp
T. 14. Frunzep-and N. She'Aldarova, Izv, IN SSMp OVI, khim, n,p 1963,p
_20l9j___L.__A*___
LaYusj_,X.-1.--bissonoY __Ne--Aw- Adrova,--apd--M-6--Ho---K6t6h-.-
-Plast. massy, 1965, No 89 3h)o
The x-ray diffraction 4tudy was perform-d using instrument UR~-50iwith
goniometer
GUR-34djusted for,measuremients at small angles.- It was-e"t
idi5_hsd-that-a-.3-hr. ----------
-thermal- treattofit- it_16W_iivufCi71_n&lmoat.totA amorphization of the
structure., as:
be.seen in Fig* L However) it also -leads to a two-f old rise of
tenacity and a
-112, UDGt 6 8 ols53+61#,
_1[~ ~---77
cwd 2 2

ACC NRt AP7011355 SOURC9 CODEt UR/0062/66/000/010/1824/1828
AUTHORt Adrova, N. A.-;' Prokhorova, L. K. Koton, M. F..
ORG: Institute of 111gh-Molecular Compounds, Academy of Sciences USSR
(Institut vysokomolakulyarnykh soyedineniy AN SSSR)
TITLEi Production of now polymers with dibonzophosphorimidazoline
links
In tho principal chain
SOURCE: AN SSSR. Izvestlyn. Seriya khImIchnskaya, no. 10, 1966p
1824-1828
TOPIC TAGS: polymer heat resistance, aster. polycondensation
SUB CODE: 07
ABSTRACT: A number of heat-resistant polymers containing
dibenzophospho-
rimidazoline links in the principal chain were produced by
polycondensation
of 3,31-diaminobenzidine with tetraphenyl esters of
phosphorus-containing
acids in equimolar quantities with heating for two hours in a stream
of
inert gas at 250-2600 C. The phenyl esters included
triphenoyyphosphine,
diphenoxychlorophosphine, tetraphenyl ester of pentamethylene
diphosphoroUS
acid, tetraphenylpyrophosphate and tetraphenylpyrophosphite. The
resultant
materials show thermal stability with heatinR UD to 400'C-1 The
aithors
Card 1/2 UDC: 54*_.64+_54l.(j+547.7+66l.7l8.1

ACC NR: AP7011355
thank Yo. I. 11ol(rovskly for taking the Infrared
spectra of the0lymers.
Orig. art. has: 2 figures, 5 formulas, 1 table.
[jVRS: 40,35V
Card 2/2

AIX NRI AP7002974 0 SO URCE COD E: UR/0413/66/000/024/0070/0070
INVENTOR: ....Adrova,, N. A.; Bessonov, M. I.; Dubnova, A. M.~'
Koton, M. M.; Moskvina,
Ye. M.; Rudakov, A. P.
OAG: none
TITLE; Preparative method for polyimides. Class 39, No. 189574
(announced by Insti-
tute of Macromolecular Compounds, AN SSSR (Institut
vysokomolekulynr-nykh soyedineniy
AN SSSR)l
Izobreteniya, promyshlennyye obraztsy, tovarnyye znaki, no. 24,
1966, 70
TOPIC TAGS: polyimide, heat resistant material, elastic material
ABSTRACT:
An Author Certificate has been issued for a method of preparing
polyimides
having high elasticity and high heat resistance. The method
involves
polycondensation of 3,3',4,4'-biphenyltetracarboxylic dianhydride
with
hydroquinone bis(4-aminophenyl ether).
,SUB CODE: IV SUBM DATE., 180ct651 ATD PRESS: 5112
Card 1/1 UDC: 678.675

AD-ROVICZ. Istvan
Deformation of the customary indexes of the working
time utilita-
tion in case of reduced working time. Munka szemle 6
no.6:
18-22 Je 162.

APRUSFKO, At me
~2419. ADRUSMY0, A. M. MAatcrinly pa biologii Alsophylex pipiend
lieuch.
bjidleten' LeDirgT. g06. UL-ta AM- Zhdpnovs, No. 23, 1949, s-
n.5-39-Bibliokr: '9, na-v.
SO: Letopis 'Z7hu-rial'nykh Statey, Vol. L14

ADRYKHAYEV9 A.M., dotment
Dynamics of changes in the fundue ocull in the
treatmbnt of
hypertension with apressin and ganglionic blocking
agents.
Sbor. nauoh. trud, SOGMI no.14sI70-177 163, (MiRA
1839)
1. Iz kafedx7 obahchey terapi! Severo-0.9etinskogo
meditsitskege
instituta.

SMIRNOV, V.A.; ADSKAYA, I,N,,- BAWWW, L.I..
Calculation of the gas consumption levels in
film-iing urban gas
supp3Y systems. Gaz. prom. 6 no.9:29-33 161. (MIRA
14:12)
(Gas diatribution)

,SMIRNOVP V.A., kand. tekhn. nauk;_AD~~ATA, inzh.;
BAGRAWAN, L.A.,
inzh.; CRERKASOVA, A.Ya., inzh,
Optimum distribution of differential pressure in 1-p
annular
systems. Ispoll. gaza v nar. khoz. no.2:133-138 163.
(MIRA 18:9)
1. Laboratoriya tekhniko-ekonomicheskikh izyskaniy
Saratovskogo
gosudarstvennogo nauchiio-issledovatellskogo i
proyektnogo
instituta po ispolizovaniyu gaza v narodnom
khozyaystve.

SMIRNOV, V.A., kand. tekhn. nauk; ADSKAYA, 1,N., inzb.
Method for calculating the optimum number of gas
distribution
stations. Ispoll. gaza v nar. khoz. no,2:11.39-145
163.
(MIRA 180)
1. Laboratorlya tekhniko-ekonomicheskikh izyBkaniy
Saratovskogo
gosudarstvennogo nauchno-isaledovatellskogo i
proyaktnogo
instituta po ispollzovaniy-a gaza v narodnom
khozyaystve.

SMIRNGVj V.A.1 ADSKAYA, L.N.; BAGRAWAN, L.A.;
GOLIX, V.G.
Technical and economic Indices of mmicip&I
distribution
of liquefied, petroleum gases. Gat.prom. 10
no,11130-33 165.
(Mlp,k 19a)

KULAKOV, D.V.; CC11KIN, F.V.; URPOVA, V.V.; S.WKINA,
N.V.; YAGUDIN,
Z.Kh.; GMENSHCHIKOVA, N.F.; CHEREITSHKIPA, V.M.;
YELISEYEV,
I.A.; CHERVYAKOVA, A.P.; BEREZOV, A.A.; MTVOVA, A.I.;
SILKIM,,
I.V.; NOVIKOVA, V.P,3 TANOVA, V.P.; UBSV91AYEVA,
_,.~1.M.;_DRYUC11TN, A.P., otv. red.; KONDRASHOVA2
V.I.,, tekhn. red.
(Economy of Saratov Ptovince in 1960; collected
statisticollia-
rodnoe kboziaistvo Saratovskoi oblasti v 1960 godu;
statistiche-
skii sbornik. Saratov, -')s.stat.izd-vo.,1962. 325 p.
(MIRA 15:9)
1. Saratov(Provinco)Statisticheskoye upravleniye. 2.
Nachallnik
Statisticheskoeo upravleniya Saratovskcy oblnsti (for
Dryuchin).
(Saratov Province-Statistics)

SHUROVSKIYO V.G.; VLADIMIROV, VJe; G-UTYSHERKO, G.I.;
KMOCHKIN, A.F.;
SHGHURCYVSKIY,, Yu*A.; ADSCV, R.I.; GOLOVKOF V.V.
Sow physico-chemical properties of charges for and the
products of
the electric smelting of Dzheakazgan. copper
concentrates, Izv.AN
Kazakho=,Serezets, obog.i ogneup. no.188-13 161. (MM 146)
(Dxhezkazgan-Copper-Blectrometallurgy)

ONAYEV, I.A.; WROCHEIN, A.F.; A.L.; ADSO!', NI.I.;
GOI-k)VFO, V.V.;
KRUTASOV , V.I.
Smelting of the Balkhash conver concentrates with
an oxygen-
enriched blow in cyclone furnaces. Vest. AN
Kazaldi. SSR 2).
no.1-27-34 Ja 165. (MIRA 18:7)

MEET, A.L.; (VAYEV~ j.A.,- -NUIT.
ADSM, Mop Go"C'U"), V.V.
Liquative electr1o ameltLng of ft~ezkazgwn copper
-ionLnn-
t-rates with the prodiction of high calcium slag.
'i-rudy
bst. met. i obog. AN Yazzakh. SSR 8V,0-49 063 (MITIN
17%8)

ACCEISSION NR! AROW18
SOURCE.i. Ref. zh..Metallurgiji-*-Abej-5i4o8
AUTHOR: Kristallf He M.t Adu!~~"~.,N*,A*; govetnikovat Yeo N.
TITLE: Investigation of corrosion stability of electric welded pipes of
steel
lKhlfiN9T
CITED SOURCE: Tr. Vaes. m.-i konstrukt. in-t khim. mashinostr4i vy0pe 45,
1963'
3-15
TOPIC TAGS: corrosion, corrosion stability,'electric welded pipe, welded
pipe,
steel ipe, intercrystalline corrosiont M18149T steel
p
TRANSLATION: Electric welded pipets of steel IKhIBN9T in state of
delivery do not
possess inclination to intercryetalline corrosion if they are prepared
from tape
not inclined to 'this form of disintegration. Stability of pipes against
inter-
crystalline corrosion after tempering at 6500 'can be ensured by
adiitional cold
rolling of pipes and use for their manufacture of tape with content
040.08% and
ratio of TI:C-*X-5. Electric welded pipes.6 not possess increased
inclination to'
Card 1/2

L 32800-66 EdT(m)1EWP(t)1ETI IJP(c) JD/W13
ACC NR: AP6012587 SOURCE CODE: UR/Ojl4/66/000/004/0036/0039
AUTHOR: Kristal't me Me; Kh A.Lu~N~.A.
ORG: none tK
TITLE: IC,~orrosion sistance of two-layer metals
I "
SOURCE: Khimicheskoye i neftyanoye mashinostroyeniye, no. 4,
1966, 36-39
TOPIC TAGS: corrosion resistance, bimetal, corrosion resistant
metal
ABSTRACT: The paper reqxirts on tests of coriRgion resistanc?~of
1) two-lay,e~ metals with
I '.
the cladding layeroade of the steels Khl8NIOTPKhl8Nl2M2T)
Khl7Nl3M2T.i hnd
OKWN28M=T,~ -2) I~Pld jo;'nts of thi--same she'ets; and 3)
tw9rlayer metals with the clad-
ding layer made of Ni M3SINpper, No. 0. 4 bronze, and LWbrass, In
all the cases the
.corrosion resistance of the two-lVer metal proved to be
approximately equal to the corro-
sion resistance of the pure metal Wen when the joints exhibited
fissures of transcrystallite
.character Some of the inVestigations were carried out at the
NIlkhimmash in conjunction
Card 1/2 UDC! 621.9-419:620.193..001.5

GUSBINOV~ G.D.j AXHUNDOVp G.A.; ALTWAj M.1l.j
ADULLAYLT, G.B.
Keotrophysioal properties of TlSa mignla
P,-.rtala. 15T.
AN SSSR. Sar. fit. 28 no.St!323-1327 Ag, t64 (MIRA
1718)

ADULIAYAEV R.N.
Principal geological and petrographical features of the
M65020iC
granitoid intrusives of the nort.1 eastern Lesser Caucasus
(Azerbaijan).
Sov.geol. .4 no.6:58-70 Je 161. (KIRA 14:6)
1, Institut geologii AN AS'SSR.
(Caucasus-,Geology, Stratigrapbic)

NIKOLIC, Z.; ADUMS 0.1 RALMEVIC, 1.
Evaluation of the Inoidence of accidents as a basis
for preventive
measures in coal mining industry. Arh. hig. rads, 15
no-41405-412
164,
1. Institut za m-ediainu rada , Sooijallisticke
Republike Srbije,,
Beograd.

ADUM, Ognjan, dr.
Some experiences with health educaticn jr; 11-fed'.
glas.
18 no.3-.90--91 Mr-Ap 164.
1. Institut za medicinu rada SocljalJstj.ckc
hapublE~e Srbije
u Beogradu (Direktor: prof. dr. D. Karajovic);
Zdrav5tvana
stanica Radloindustrije "Nikola Teslall u Beogradu
(Upravnik:
dr. 0. Adum).

YUGOSIAVIA
ADUM Dr Ognjan; and VA-RKOVIC, Dr Miodrag; instil-ifte of
Occupational 14~di-
c- 'L~
, ' EZAA'~'epublic of Serbia (Institut za
fEe-. oc a medicinu rada SR Srbije)
Hencl (Dir--ktor) Docent Dr Milos KILI--BARDA,* and Medical
Department of Public
Transit Agency of City of Belgrade (7Ara-,rstvena stanica
Gradskog
saobracajnog preduzeca) Head (Upravnik) Dr Dragan JOVANOVIC,
Belgrade.
"Protecting the Health of Transportation Workers."
Belgradep Narodno Zdravljc, Vol 21, No 8-9, 1965; pp 257-264.
Abstract : Very thorough analysisof the many reasons why
traffic accidents
have been increasing very sharply in both frequency'and
severity over the
course of the recent years in Yugoslavia: professional drivers
and tram or
trolley or bus conductors are incredibly overworked, as some
of them may
work 7 days a week for months on end, often with overtime at
night too;
then the noise, temperature; many of these and other noxious
factors are
analyzed and discussed in detail, as are some proposed
corrective steps.
Graph, 4 tables; 5 Yugoslav and 8 Western references.
21 -

a -
M.
Dynamics oil the activity of thiamine and riboflavin in
edible green
plants at various developmental stages (in Armenian
with summary in
Russian). Izv.AN Arrm.&U.Biol.i sell khos.ilauki. 4
no.5:423-429 151.
(VITUM-B) (GRMS, IDIBIS) WU 9 -. 8)

ADUNTS, G.T.
Anhowpir
Dynamics of the amount of ascorbic acid and carotenes
in edible
green plants at different stages of development (in
Armenian with
summary in Russian]. Izv.AN Arm.SSR.Biol.i
sellkhoz.nauki 4 no.6:
527-532 '51. (Niah 9:8)
(Ascorbic acid) (Caroteass) (Caucasus--Greens, edible)

ADUNTS, G. T.
...-OPPOM
Dynamics of the amount of vitamins in some cabbage
varieties
cultivated in Erivan [in Armenian vith summary In
Russian]. Izv.
AN Arm.SSR.Biol.i sellkhoz.nauki. 5 no.2:83-87 '52.
(HLBA 9;8)
(BRIVAN--UBBAGE) (VITAMINS)

77
6 t1i $4,C34
WIAtter iip~ ud
amirit Wrim.). Abovp th4t (!01~ztlon ill th.
-TUt 4-aun Im Win jjuri~dm-- w mmam~- jm4
wd
itIi Y.-t
ef
27

6 T.; OGANESM, A.S.
Zffect of severin& the va-gue nerve on diurests and
renal filtration.
1xv.AH Arm.SM.BidIA,s6l'khoz.nauki 7 no.10:65-71 0 154.
(KLRL 9-18)
1. Institut fiziologii AN Armyanskoy ISM.
(VAGUS MM) (11MYS) (DItMTICS,M DIURESIS)

USSR/Human and Animal Physiology - Sensory Organs. T-11
Abs Jour : Ref Zhur - Bioll, No 7, 1958, 32253
Author : DanirchoGlyun, G.G., Adunts, G.T., Avakyan, Ts.M.
Inst . ...........................
Title Action of Radioactive Phosphorus on the Functional
Dondition of the Retina of the Eye.
Orig Pub izv. AN ArmSSR. Biol. i s.-kh. M.) 1957, 10, No 2,
3-13-
Abstract Imersion of a preparation of an isolated froc, eye
in a
solution of %2~uMIN04 (strength not -.-ndicated) caused
stronger depression of ERG than di immersion of the same
in a solution of 1&2HP04- Someti, s depression of ERG
preceded an increase. With subcutaneous introduction of
Najjp320 4' impairments of the ERG (removed also from the
isolated preparation) set in only through four to ton
clays after the introduction. In addition, the accumila-
tion of p32 was the same in the retim of an exposed and
unexposed eye.
Card 1/1

ADUNTS, G.T.
Effect of x-radiation on glycogenic function of the
liver.
Izv.AN Arn.SSR-Biol.nauki 12 no.4:49-54 Ap '59.
(MIRA 12:9-11
1. Sektor biolchimii Akademii nauk ArmSSR.
(BBTA RAYS--PHYSIOLOGICAL EFaCT)
(LIM--GLYCOGEIIIC FMICTION)

-ADUNTS, G.T.; XMBSrAN, R.R.
Glycogen content of a chick embryo on different days of
develop-
ment. Izv.AN Arm.SM Biol.nauki 32 no.11:15-23 N 159.
(MMA 130)
1. Saktor biokbinii Akademii nauk ArmSSEI.
(OLTOOM). (INRY-OLOGT--BIRDS)

BUNYATYAN, G.Kh.- ADUNT".Z-~
Changes in the polyphosphatase activity with relation
to inorganic
polyphosphates during the development of a chick
embryo. Vop.
biokhim. 1:149-160 160, (MIRA 141-12)
1:,Department of Biochemistry, Academy of Sciences of
Armenian
Erevan.
(FOLMOSPHATASE) (FUM OLOGY-BIRDS)
I

ADUM, G.To; NERSESYANp R.R.j CHALABYAN., G.A.
Aotivation of Amylase by bile. 127, A# Am. SSR.
no,lOiW-99 160.
1. Sektor biokldmii Akads~ii nauk AnnSSR.
(AMYLOB) (BILE)
Biol. nauki 13
(MIRA 11112)

ADVNTst G 11ANYAN, I.G.
--- ~,T.;,AS
,- --- ----------
Activity of inorganic polyphosphatases, Izv. AN Arm. SSR.
Biol. nauki
14 no. 4:79-85 Ap 161. (MIRA 14:4)
(PHOSPHATASES) (FliBRYOLOGY-BIRDS)

ADUNTS, G.T. -- NKSMYA11, R.R.
........... .
Amylase activity of bile. Izv. All Arm. SSR. B-1ol.
nauki 14 no.8;
47-53 Ag '61. (MIRA 11,: 9)
1. Sektor b-iokhimii AN Am -- k y $SR.
(A,.,.4,,1,)v'mu 0 (BILE)

ADUIM.. G.T.
-
Reactivation of sops- phwiphomonoesterases after
their
denaturation by hes);. Vop.blokliim. 2:129-137 16",
"IMM 15212)
1. Institute of Blochendstry,, AcadexW of Sciences
of Armenian
5,30R*,, Erevan, (Phosphatase)
(Reat-Physiological effect)

ADUNTS, GaTo
Dynamics of phosphomonoesterase activity in the
develqp"nt of
a chicken ermbryo. Vop.biokhim. 29139-152 161. (MmA
1521"')
1. Institute cX Biochemis~x7q Acad-i!jW of Sciences
(,f Armenian
SaS*Re, Erevan#
(Phosphatase) (En'bryology-Birds)

ADUNTS.,_G.T,; HERSESUNt R.R.
Changes in the amylase &M phorphoi7lase activity in
the
development of a chicken embryo. Vop.biokhim.
4'-s153-158 161.
(MIRA 15:12)
1. Institute of Biochemistry, AcadeW of Sciences of
Armenian
S.S.R , Erevan.
i.Uwlase) (Phoophorylase) (Embryology-BirdB)

ADURTS $ G. T.
Specific differences of phosphomonoesterases. Izv. AN
Arm. SSR.
Biol. nauki 15 no.lt4l-51 A 162. (MIRA 15:2)
1. Institut biokbinii AN Armyanako SSR.
(PHOSPHATASEff

ADUN �,.~ SARKISYAN, L.V.
Change in the activity of phosphomonoesteraseq
related to the
preservation of the homogenate. Izv.AN
Arm.SSR.Biol.nauki 15
no.7:13-22 Jl 162. (MIRA 15: 11)
(PHOSPHATASE) (TISSUES-PRESERVATION)

ADUNTS, G.T.; SIM)NYAN, A,A.
Studying the dynamics of phosphoprotein phosphatse
activity during
the development of a chick embryo. Izv.AN
Arm.SSR.Biol.nauki 15
no.9;35-45 S 162, (KTIA 15 t 11)
1. Institut biokhimii AN Arinyanskoy SSR.
(PHOSPHOPROTEIN PHOS-PRATASE)(EI-MRYOLOGY-BIRDS)

ADUNTS, G.T.; NMSESYANp R.R.
Effect of gamm-ax!nobutyric acid on the phosphorylase
activity,
Vop. biokhim. 3:99-105 163. (MrRA MV)
1. ~-'nstitute of Biochemistryl Academy of Sciences of
the Armenian
S.S'R. , Erevan.

ADUNTS, G,T,; SARKISYAN, L,V,
Effect of adreiallne and serotoni-n on the activity of
alkaline
phosphatase of the liver and kidney. Vops biokhim.
3tll5-123 163,
(KMA 17 1122)
1, Institute of Biochemistry, Academy of Sciences of the
Armenian
S,S*Ro, Erevan*

ADMITS, 0.7.~ARRAMDVAO R.A.
Effect of adrenaline on the activity ol" alkaline
phosphatase of
rat kidneys (in vivo)* Vop. biokhim. ~,M5-131 163. (MIRA
M12)
1. Institute of Bioahemistry, Aaadeqr of Sc~ences of the
Armenian
S,,S,R., Erevant
N

ADUNTS, G.T,; ASLWANj I,G.
Effect of aertAln factors on the activity of
glucoce..6-phoophatass,
Vop. biokhime N133-146 163s (KMA M12)
1, Institute of Bioobemlatryo Academy of Soienoes of
the Armenian
S,S$R,, Erevan*

-ADUNTS, G,T.
Fluctuations in the actlv, t-,- of ~~ of varinus
brain nections of a oldoken embryo wider changing
1:11" of the
wi d I u n. 1'zv. AN Arin. ;~,)R. Blo.l. nfoz'ki 16
no.5.25--`,'~ M,y "63.
(mlk~L 1-1:0

ADUNTS, G.T.i ABUMOVA, R.A.
Effect of pair, on the functional activity of
alkaline phosphats-)e
in the kidneyq of white rata. Iz-v. AN Arm. SSR,
Viol. miki 17
no.2:21-32 F 164. (KiL4 37, 8)
1. InstItut biokhLmii AN Armyanskoy SSR.

ADUNTS, G.T.; A51,ANYAN, I.G.
Chani- I- +I-- -Iiiaose-6-phosphatase
(D-glucose-o'.-phosphate-
phospho.-hydrolase) activity under the influence of
adrenaline
in embryonic tissues of chickens. izv. AN Am. SSR. Biol.
nau7