SCIENTIFIC ABSTRACT NOVIKOVA, N. V. - NOVIKOVA, S. I.

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• Collection: Scientific Abstracts
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• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: August 23, 2000
• Sequence Number: 14
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

5-_5700 78090
sov/6r- -6o- i - 5o/7-y
AUT11ORS - Nesmeyanov, A. N., Bopisov, A. Ye., Novilcova,-.. V.
TITLE: Letter to the Editov. Geometrical isomera of' Propenyl
Compounds oi' Tri- and Pentavalent Antimony
PERIODICAL: 1,Zvestlya AlcadeinLt nauk SSSR, otdeleniye. khImIcheskilch
nauk, 1900, NV 1, P ill'( (USSR)
ABS'Flit%CT: The authors veport that dLlrlr)[,' tile Study Of' SteVe0-

chenitstry of organometail1c,,, , seri-es Of geometrIcal
a :1
isomers of' propenyl compouncis of tri- and pentavaient
,antimony were synthesized, and that cis- and tt,atv_;-
propyllithium react w1th ant1monv trichlorlde to Al'orm
corresponding cis- and trans- propylantimony. The
reaction between these Ujomers an(] 1-ialogen lead to the
formation of a series of' Isomers ol' pentavalent antimony:
((7113CI I - "Al').,Mv + Xi- I n-('1D3SbXz, X-Cf, fir, 1.
cls- isomers, containing C1 and Br, are crystailine and
Ca-.-c! 112

Letter to the Editor. Geometrical 1somers ybogo
01' PL'openyl Compound.-, of Tri- and Penta- SOV/b2-bO-i-3b/15f
valent Antimony
the trans-isomeps are itq~_tt(js. bi(jutd goometrica-1,
Isomevs ol' pen tap vopenylant imony were synthesized
from cis- and tvans-laomers of tripropenylanttmon,
dictiloride and the corresponding tsomers of' DropenyL-
lithium:
q-!C113(_,1 I ~ (7111.i - (Cl I.,(-[ f~-(711),Sb+ 21-Wr.
These Isomers have different refractive Indices and'
ansorption spectra. They react witti bromine, fo-ming
two tetrapropenylantIrriony bromidezi:
(Ct 13(,11 L, t. 11 h ! Br: ((A 1,C. I I -- cI 1) sf!f;r I- (',I I (" I II
Theve is I Soviet refopenoe.
ASSOCL~ITLON: Institute oC Eie-ment-Orr-anic~ Gorw,,ounds, A
Sc'ences, lj.~SR element
soyedtnenty Akadem-11 natak SSSR)
SUB1-,,1TTE!): October 29, 1959
Card 2/2

USMANOT. A.S.; BORISOV. A-To.; NOTIXDTA. N.Y.
Vinyl caftmutda of tri- and ptntavalent satimovy. lsvJX SM
otdobalmeamk 0003*52 IV 160. (=A 13:6)
1. Institut elmentoorgauichesklkh sayedinenly Akadenii naut GSM*
(Antimony compounds) (VlzWl compounds)

. I
BRE$TKIN# A.P.; NOVIKOVA, N.V.
Klmties of hydrogen perazide decomposition by catalase. Biokhlmila
.25 uo.4sO4-592J2-Ag 160o (Km 13: n)
L" Chair of Inorganic Chemletry, Sanitary-HygienLe Nedical lnstivte,,
L~nlngrm4
tiMROGEN PERCKIDE) (CLTAUSE)

NZSMZTAIIOV. A.U., akad.; BORISOV, A*Ys.; NOVIKOVA, N.V.
Atomic refraction of antimony. Dokl.AN SSSR 134 no.1:100-101
S 160. (MIRA 13:8)
1. Institut elementoorganicheakikh soyedinenly Akademii nauk SSSR.
(Antimony compounds)
(Mercury compourds)
(Arsenic compounds)

NOVIKOVA N V., -BRESTKIN, A.P., PROKOFYEW, YE. G., RaW-INA, NI (USSR)
"Kinetics of Enzymic Hydrolysis of Phenyl Phosphate."
Report presented at the 5th Int'l. Biochemistry Congress,.
Moscow, 10-16 Aug 1961.

NESIEYAMV9 L.K.; BORISOV, A.Ye.; XOVIMVL,~ N.V.
'Propenyl Ao-re-01-some- a 0 tri- and pentavalent antimony* Izv~AN
WOR 0td.Tr'%,f-.nsuT- no44:612-,617 Ap f6le (IWA 24:4)
Is Institut elowntoorganicheakikh soyedinenLy AN SSSR.
(Antimony conmda)

I
A.11*; BORISOVp A.re-; HqVIKOVA, H.V*
CoiPMAS of the tRw (RCN CR-1)3Sb 02902. Izv*AU SSSIR Otdokh4-
dmuk W.4-.730 Ap (KWA 24:4)
U. jwtitut olowntoorgamlobAskikh soyedinenly AN SSSR,,

27486
8/062
/61/000/009/001/014
BI I 7/B1 01
AUTHORS: ffeemeyanov, A. If., Bori7sov, A. Ye., and Novikova, N. V.
TITLE: Isopropenyl and vinyl compounds of tri- and pentavalent
antimony
PERIODICAL: Akademiya nauk SSSR. Izvestiya. Otdeleniye khimicheakikh
nauk, no. 9, 1961, 1578-1582
TEXT: Isopropenyl and vinyl derilvatives of antimony of the types
R Sbo R Sb, R SbX, R SbX where RuCH I CH =CH-; X a 01, Br, I, were
3 5 4 3 2; 2-9- 2
CH3
synthesized in the present work. The authors had previously prepared cis-
and trans propenyl derivatives of tri- and peatavalent antimony (Ref. 1:
Izv. AN SSSR. Otd. khim. n., 1960, 147) and pentavinyl antimony (Ref. 2;
Izv. AN SSSR. altd. khim. n., 1960, 952). Triisopropenyl antimony (C 9a 15 Sb)
and trivinyl antimony (C6H 9Sb) were obtained by reaction of antimony
trichloride with isopropenyl lithium, or vinyl magnesium bromide,
Card 1/3

27486
5/062J61/000/009/001/014
Isopropenyl and vinyl compounds ... BIITIBIOI
respectively. The compounds thus obtained react readily with halogens,-
forming derivatives of pentavalent antimony: R 3Sb + X2 ---P R3SbX2' Tri-
isopropenyl antimony dibromide (C 9H15 SbBr 2)1 a white crystalline subatance,
mop. 138PG$ reacts with isopropenyl lithium to give pentainopropenyl
antimony (C 15 H25 Sb)o a white amorphous substancep mop. 60PC. Treatment
of trivinyl Antimony dibromide (C SbBr n20 1.6480) with vinyl magnesium
09 2# D
bromide leads to pentavinyl antimony (C 10"15 Sb), a slightly greenish
liquid. quantitative analysis showed that both pentaalkenyl antimony
compounds were sufficiently pure. By treating these compounds dissolved
in CHC1 3 with equimolecular quantities of bromine at -5'c, the authors
obtained totraisopropenyl stibonium, bromide (C12H2OSbBr, leaf-shaped shiny
crystals, mop- 125-1350C) and tetravinyl stibonium bromide (CO11,25bBrl
needle-shaped crystals, m-P- 53-540C), respectively. Treatment with
equimolar qu"tities of iodine at room temperature tetraisopropenyl
stibonium iodine (C12H208bI, mop. 163-16400) and, respectively, tetravinyl
Card 2/3

27h8
6
0/0 1/000/009/001/014
7YB'1
Isopropenyl and vinyl compounds ... B117 B101
stibonium iodine (a 8a1201. m-P- 68-TOOO) in crystalline form. On heating
on-an oil bath at 1900C, p*ntaisopropenyl and pentavinyl antimony form
triisopropefiyl antimony and trivinyl antimony, respectively. This was
confirmed by bromination of the triisopropenyl antimony obtAined, respec-
tively distillation of the trivinyl antimony, which in the former case
yielded trilsopropenyl antimony dibromids, m.p. 137-1380C, and in the
latter a colorless liquid, 20 1-5595o which was identical with trivinyl
9
antimony. Trivinyl and triisopropenyl antimony react with thallium
trichloride to give trivinyl antimony dichloride (06H 9SbC120 liquid) and
triisopropenyl antimony dichloride (0 9H 15 SbC12, white crystals, m.p.
102-10300- In-this reaction thallium is transformed to the monochloride.
There are 3 references: 2 Soviet and I non-Soviet.
ASSOCIATION: Institut elementoorganichookikh soyedineniy Akademii nauk
SSSR (Institute of Elemental Organic Compounds of the
Academy of Sciences USSR)
SUBMITTED: February 15, 1961
Card 3 3

BIWTUN2 A.P.; NOVIKOVA,.N.V PROKOFIMU, Ye.G.; RZHFMIIA, N.I.
Kinetics of 'sodim phenyl phosphate h*olysis by alkaline -phoapbstase.
Biokhlallm 26 no.2:266-275.Hv-Ap ~~161. (MIFA 14-5)
Is Chair of Inorganic ChemLatr7i SaziltaryQHygienic Medical Institute
Leningimd'
ZPHOSPUTASE) (SODIUMPHEM F%SPHATE)

8M5
5/020/61/136/001,/027/037
113 o 11Y.3 B0041B056
AUTHORS: Borisov, A. Ye., Novikovap N. V., and Chumayevskiy, N. A.
TITLE: Infrared Absorptionspectra of Organometallic Compounds of
the Ethylene Series. On Cis- and Trans-configurations of
Propylene-antimony Compounds (Sb'II and SbV)
PERIODICAL: Doklady Akademii nauk SSSR, 1961, Vol. 136, No. 1,
Pp. 129-139
vestigations of the infrared
TEXT: The present paper is an account on in
absorption spectra of cis- and trans-isomeric propylene compounds with
tri- and pentavalent antimony. Synthesis of these substances was describedin
an earlier paper (Ref. 1). investigation was made with a OVIK(_ M-3 (VIKS
M-3) spectrometer and an NaCl prism within the range of 700-1800 am and
with an qKC-12 (IKS-12) spectrometer and KBr prism within 400-700 am-
Figs. 1-3 show the spectra of
(CH 3g 3SbBr2 1 (CH 3~ .~)3SbBr.; of the aorresponding
Card 1/4

as -ty
Infrared Absorptionspectra of Organcoetallic
3/020 61/136/0W/027/037
Compounds of the Ethylene Series. On Cis- and B004YB05'6
Trans-configurtlions ofVPropylene-antimany
Compounds (Sbi and Sb
chlorides and iodides, moreover of (CH,9 -~) Sb; (CH - Sb;
Ij H 3 3~_ ~) 3
(CH 3g= 9)5Sbj (CH 3r 9)5Sbj (CH 3g= 6)4SbBr; CH 3P_ ~)4 SbBrj and, for
H
H
comparison, sketches bf CH 3-0-b-Br and CH 3_9=X-Br spectra. Frequencies
arelisted in Table 1. All trans-configurations exhibit intense absorption
at 945-970 am- . The frequencies of the CH-group uneven oscillations %re
at 971 cm-1 for tri- and pentapropenyl antimony, at 945 am T for dihalogen
derivatives, and at 967 cm-1 for tetrapropenyl stilbonium bromide. The
trans-configurations are distinguished by bands at 18-726 cm- which do
not exist in the cis-configuration. The 920-940 am- absorption bands of
the cis-configuration are considerably less Intense than the 945-970 cm-1
absorption bands of the trans-configuration. Only cis-tripropenyl antimony
and cis-pentapropenyl antimony turned out to have bands at 970 cm-1, but
their intensity amounts to only one third of the trans-oonfiguration
Card 2/4

Infrared Absorptionspectra of Organometallic 5/020/61/136/001/027/037
Com ounds,of the-.Ethylene - and B
p Series. On Cis 00413056
Trans-sconfiguritions of-Propylene-antimony
Fi.
..~Gom ounds .(SbI,II,'.and Sb V)
p
-Th
intensity. asame holds for propenylbromide: Intensity of the 930 am-1
on
band of the cis-configuration only one third of the trans-configurati
band. The bands at 655-660 am-1 of the cis-configuration.are 2 - 2.5 times
more intense+:than.those of the tran -configuration. Cis-configurations of
the halogeii.,derivatives and of tetrapropenyl stilboniumbromide showed
1ntensebands at.452 cm which were.not observed in the case of trans
i as 'And ci - and trans-tr and peatapropenyl antimony. The
configurat, a a
plane~vibrations'at the:double bonds -are more intense at 1200 cm-1 in the
case of'.trans- .isomers and at 1300 am -lin the case of cia-isomera.
Yeameyanov is mentioned in.th.e.paper. The authorg+,thank Academician,
V.-Obreimov for his interest,in the investigation and R. A. Isayeva
Ye.'D. Vlasov for their collaboration. There are 3 figures, 2 tables,
1 US, and 2 British.
and 8 references: 5 Soviet,
ASSOCIATION.-:1natitut elementoorganichaskikh soyedineniy Akademii nauk
rbunds of,the
SSBR.(Instituts of SlementalOrganic Comp
-Academy of Sciences. USSA)
~Pard3
p

Infrared Ababrptionspectra of Organometallic S/020/60WOO1/027/037
Compounds.of the Ethylene Seri es, On Cis- and BOO4/BO56
Trans-configurtlions of Propylene-antimony
V
I
.
Compounds (Sb and Sb
)
PRESENTEDC July- 18, 1960, by I. ~ V. -Obreimov, Academic ian
~~SUBMITTM.~ June 16, 196o
-Legend to table 1 . Frequencies
i of the SbIll and Sby propenyls. 1) Cis,
't
ani, :3) b
r s oiling point,
4)

elting *Point.

clfl~i
l;CH)e
(11lf,CH_CH)G-
(Cff.CH-CH) .l- ll_CH),.
~&f ~ (MCH-Cli), (CH.CH~Cjlj. 5b
. .
s -SKIS
vp (C-,
J JIL I
1
. J

. IGO-

. Wl~j

G&-

'i22 V. na.

140-

. X19"

V
TP
.
T. 1(11n.)/
7V tG7!14 1 3
2 .1431

a ,

(kw. 4

IGO.
1600
loor.
1607
16"
W5 040 1508
16W
NO tGoo IGO
1 4M 1442 1444 1440 1 3~

2 W4

1 .14 25
8 H37 -
13' 3 1445
M 143?

N7 1
1 140:
%) .1437
IM

t
i
ra
3w
: I
Ig
His
fus jr
.6
M
1
1365
134A
M .
07
13(a
,
YJS
34A
I
1
.
321
1368
1 193 1199- 1201 1191 190 Ifto- It IG 1195. 1195 1223 I M0 1190
ills Ills -
105
1065 110
105 -11 00 106
1 04Z 1109
104S 1165
1062' Ills 1110
f062
1039 1000
10.10 1047 M2 1041 1040 1030 1043 W35 V90

970
971
0140
957
!M9
251 .
037
s
1A5 w0

92A 967

w 070

M
va
935 M

C45

u 025

-
1
72 u

-
718
700
726
E ou

722
710
No 720
-655 6:,.5 667 W .
03~ '660 6GO 660 3
0 GQ,

'
qard 4/4 610 620, .610 613 M 6
!
ON
.
-
,,: IAZ W . ......

.3/06:?/63/000/001/024/025
101/B166
A
AUTHORSs Noomeyanov, A. K., borinov, A. Ye., anA Novikova, N. V.
TITLE: Diphenyl stibine
PERIODICALs Akademiya nauk SSSR. Izventiya. Otdoloniyo khimicheskikh
nauk, no. 1, 19639 194
TEXT: Reaction of diphenyl antimony chloride with lithium aluminum hydride
in anhydrous ether under an atmosphere of argon, produced the hitherto un-
known diphenyl stibine ' (C 6H5),Sbfz, in 500A yield, colorless liquid, b.R.
20
115-1200C/0'.5 mm Hg, n 1.6882, which quickly.decomposes in air with for-
D
mation of a precipitate.
AS 5 0 C I A TIO!i-:-_.- e- me -t'6'-6 rg-a-n-1-c heskikh soyedineniy Akademii nauk SSSR
(Institute of Elemental Organic Coopounds of the Academy' of
Cciences USSR)
SUBMITTED: November 27, 1962 1
Card 1/1

BMISOV, A.Ye.; VaULZI -.9- tESMIANN, A.M.
Trial lylatibins. Izv.ANWM.5er.khix. no.&1506-1507 Ag 163.
(=A 16s9)
110- Inistitut elementoorgwdehaskikh soyedlmnLy AN SM.
(Stibins)

.:,/C120/63/148/006/015/023
B117/~186
'AT A. ff., Academician., Borisov, A. Ye., Novikova, N. V.,
JTROSSs Nesmoyanov,
Chu=yavskiy# N. A.
ftMs Infia-roid absorption spectra-of stereo-isomers of propenyl-
-lithium
tPERIODICALs Akademiya nauk SSSR. Doklady, v. 148, no. 6, 1963, 1312 1313'
TEXT s Infra-red absorption spectra-of cis- and trans-isomers of propenyl-
lithium were,, studied- - more -accurately. in compariuou with the results ob-.
in a 20% other solution) earlier (DAN, 119j, 712 (1958)) by the
same authors and with those of N. L. Allinger and-R. B. Hermann (J. Org.
hea.9 26, -1040 C1961)). In order to eliminate the misleading frequencies
C
by which the other is characterized, the spectra mentioned were taken both
other solution and in paraffin oil. A comparison of the spectra taken
.~An this* media showed the following-frequencies-to be consistents
625~ a 1540 and.1300 ca- n spectra of the din-isomer; 1635 ca-
a -ca
550 the spactrum, of the trans-isomer. Hence the higher frequencies
th*-. lnfra~-r dspectrum of propenyllithium of the C-C oscillations

NESMEYANOV,, A.N.; BORISOV,, A.Ye.; NOVIKOVA, N.V.
Trialkanyldialkyl and trialkenyldiaryl compounds of antimony.
Izv, AN SSSR Ser. khim. no.7:1197-1202 Jl 164.
(MIFIA 17:8)
1. Institut elementooreanicheskikh soyedineniy AN SSSR.

~L~~- EWT(M)/EPF(C)/EPR/FWP(J)/1T P,, - 4//,D r - 4/P S - 4.3 S D/.kE DC ( a ~ /A 3 D ( p3
A"-(' 7ESSION NR- AP4042870 W/R IV, S/0062/64/000/00'71/1262j'12(19-
AUTHOR: Nesmeyanov, -A.--N. ; '.~3orisov, A. Ye. ; Novikova, N. V.
TITLE: Pentaalkenyl compounds.of antimony
SOTIMM, AN SSSR. Izvestlya. Serlya khimicheskaya, no. 7, 1964, 1202- 1209
TOPIC TAGS: organoantimony compound, pentaaken yl antimony, pentacovalent
;.;numony compound, synthesis, penta~sopropen '-vlanumony. pentavinylantimony,
',~er-nai stability, halogentation, brominat4on, lodination, trialkenylantinionydi-
bromide, pent ana phthy !ant i mony, exchange reaction
ABSTRACT: Cis-propenyllithfum, trans- propenyllithium, isopropenyllithium
and viry1fragnesium bromide were reacted with SbC15 to form the pentacova1ent
__&_ I-&-- -dTl

ACCESSION NR: AP4042870
moted gas evolution and formation of the tri(cis- or trans- p:-openyl) antimony,
16--h-,"~ th- fi~~iiii~ed m - . -,,.- . , -, . :-- I- I ..~ ; ,
-w-ii- 6 ant
w1i 6 the trimis-propenyl) imony dibromide (V) or
tri(trans-propenyl)antimony dibromide M). Reaction of I or 11 with an equiva-
lent amount of iodine gave the tetra (cis- or trans-propeny0stibonium iodide.
AA four initial compounds reacted with 2 moles of iodine to form the correspond-
~n2~ Deriodides: R,.S'f)l. 19. Reaction of the I e ~raalkenvl sti Finn iiirn hrnmiri,-q with

L 14335-65
ACCESSION -NP,.: AP4042870
ASSOCLATION- Institut elementoorganicheskikh soved"nenly Akademii nauk SSSR
ir tute of Org
metaUic Compounds Academy of Sciences SSSR)
ano ---------
SUBTvUTTED- MovU ENCL: 00
Card 3/3

NOVIKOVA, N.V.; PROKOFIYEVA, Ye.G. (Imningrad)
Comparative evaluation of vwious methods for determining the
activity of alcalins phosphatase. !Ab. delo no. l2s713-716 164.
(MIRA 1811)

L .27093-65 M1(m)/EPF(c)/EWP(j)/T Pc-4/Pr-4 RM
ACGMSSIOW-Mi AP5022459 UR f0W /65/000/004/Cr/63 /0763
542.957
AMCPSi Neameyanov. A. N.; E~qrisov ikcva, N. V.
~qr A. Ye. Nov
TITU:-, Organometallic derivatives of -~hu-ien,
Seriya khimicheskaya, no' 4, 1965, 763
TOPIC TAGS: organo metallic compound;. ethylene, organic synthesis, antimony
LIRSTRACT: The authors have synthesized dimetallic derivatives of antimorq and
9'hylene by combining organometallic A.-rdrides with or-ganometallic monoacetylides
af~ccrding to the schemei
CA 1 '1 7' A )I
CIX 161 -~- (n.C,jj,~2 S.1
nils at 1001-10W (2.5-10-3
the -e3uiting 1,2-bio(n-dibu".ylantimoriyl)ethylenel-.~

L 5?093-65
Measized aQWsjtjcn,(Jn %) gave 42.49 and 42.23 C)
7.51 and 7.68 H, and 48.33 and
18H3SSb2. Computed percentages were 43.41 Gy I
3b; C 7.60 111, and 48.90 Sb.
simllar fashion (C h )2SbCB=ClBb(C if n) vas obtained from dipheny) antimo-
6 5 4 9- 2
nous an~Tdride and di-n-butyletbMl rantimcny. Boiling point is 147-150C
r"lo-3 n20 %
mm): D 1.5960. Measured compos4tion "in %) -ave 48.66 and 48.83 CP
b.Z6 and 6.23 H, and 44.06 and 43.89 Sb; C2-2H 3(P32, Compute-i composition gave
49-09 G, 5.62 H, and 45.27 Sb. Orig. art. has: 1 forw-la.
ASSOGIMONS Institut elementoorganicheskikh soyedinenly, Akadem'ii nauk SSSR
(Institute of Organoelewental Compounds, Acade-Wof-ScienceslSiSSR)
-T-ED: 2LFeb65
IBM - EjNGL- 00 SUB GCDE: OC, G C
NO REF SOVt 001 OTHERs 004

XMYAIW,g A*Nt akitdso&; BMISQVt A.Tool _KCffXq*,O. 5.V.
Goometzle - Sm plu"Im aMmayl -eampouWas Dekl. AN SWR
165 20,21333-336 5 f6se (KMA its 11)
1e limotilat elan - a AIM se7edliardy AN SSSR,,

NOVIKOVA, N.V.; YEVSTIGNEYEV, V.B.
conditions for photophosphorylation in extracts from the
anaerobic sulfur bacterium Chromatioum. Biokhimiia 30 no.6:
1245-1250 14-D 165. OATMA 19: 1)
1. Institut fotosinteza i Institut biokhimii imeni A.N. Bakha
AN SSSR, Moskva. Submitted March 29, 1965.

S4DURCF. CODEt URI OZ 16[66[G3 L/0031046310461-
AUTHOR: _j~;otip_ya N. __FrokoEfeva, E. G. ..... .
_*_._._Y~jjrokof tyeva,, Yee G.
ON: Sanitary-Hygienic Medical Institute, Lenkrgrad (Sant tarno-S 16iyant cheskly
TITLE: Kinetics of stmiltaneous hydrolysis of phenylphospliate and glycolphasphate.;.
under the action
oUalkailna phosphatase,
SOURCE Blokht Iyat v. 31g no. 31, 1966, 463-467
A
TOPIC UGS: hydrolysis phosphatase, organic phosphate
SUB CODE: 06,07
ABSTRACT: In view of an earlier Investigation by Yu. G. Zhukovskly dealing
with the simultaneous hydrolysis of phenyLphosphate and glycolphosphate under
the Action of acid phosphatase, the authors considered it of interest to conduct
an analogous investigation with alkaline phosphatase. It was found that under
the very some conditions (370, 0.075 H carbonate buffer, pH 10, concenLrat-lon
alkaline phosphatase preparation 0.004 mg/ml and substrate concentration 2
mtILIntoles) the rate of enzymic hy~rolysia of sodium gXycolphosphate is alnost
32-fold less than that of sodium phenylphosphate, 1. e. much less than for acid
phosphatas 6 and V are deter
a according to.Zhukovsktyts data. The quantities V
mined Co both_st&stratesi:-.It was found that when both''So
3 3
;cwd., 112

ACC NR.- AM124U
der Edentical conditions,phanylphosphate displays strong Inhibitor action In
to glycolpftasphateq, ~rkl to th* latter h&$, practicat ly no such effect
-a~vls ON"w1phosphato. r mittfng cmvutation of th*:
-*Wtims ire doriveo po
'Li.ratwof iftw*l6lydmIysIs wg-eacb:of the, esters'mhen'.etthe,
r or both are r*s'"
ifil the zeactlimi 2'f -CJFRSu~ 40*42b
Yn'
~!4
zil
f -
T
Y
1-4
ti

,GLADKOVAg A.I.; MOVIKOVAI, N.V.
Use of omid in h)pertension of endocrine origln. Pat. Ifitiol.
i eksp. terep, 9 uo.N60-61 My-Je 165. (IWJRA 18A 9)
1, Mel fisiologli (xav.- prof. B.A. Vartopetov) Ukralnokago
instituta eksperlsentallnor andokrinologil, Kharlkov.

BLYUG?;Rs AQF9 $- WSHaLVICH, ru V - KOVSH, G.T4L 2- GLUDYNISIII.E.P.1 NOVIKOVA,
O.A.; FAVLOVSKAYA, A.I.-;.fZRAMT, LX; U=, B.A.
Bicillizb.-3 and its clinical use, Sav.wd. 25 no.7-. o6i.
15:2)
1. Institut orgwddhssjWgo~L)9inteff& AN I#W fMz4wkfiy
T infIt Rishakaya g~co4"yadot*k&ya Til-InIcheskaym
MOCUtaiiWki. AtUt JL
bollnitsa.
(BIGI

0 # 0 fee G* 0 so 00 00 e-9
f'0 a * 0 4 fff~O
(#&I;;u gu.& XajL1q;r-1t tra wis it a a Q (I MIT itaeg
It,
j_A A
4.0 moctl4s Aq(S
frl!y
V4" ,-00
4
V4d W..ftad ift.6.1 -9-d
lot.,
ift
- 1, stad Ce W" kwd Pmd*MW-Odiy
NJ
St
144 J;
.~i, - Tam.
it 00610.11,0VID
ion in 014d On aftef*4 am bY C* &Wwg tmPmf
00 (wim (MWWIM C4% did Wt 00
ag. a - Tbe
ed's
Mr. Ca hmpamd
00
WEI tf
ber&WO.
111C on"- d jaggagaw pasibly,
Joe (4rMpCriV c
(mm
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-00
tMp.: CA Ow stabMir cc askelitc 08 clud-
a Joe and N'kpwnd wmAwW the budaM Of b-demA
ragrAmica (d a bad, W" dkp-td PM__
if the bardmew owd md' see
bwmw- the Wittie-
bl. it -I- W--d
britdcam JrKnowd with tW
(it
C4. lamej
hWAId to
amuld be takm ta pm-t it
ugh temp, too
Los
floo
p "o 0
#MOON* get*", Nik'"T 04C
V 7r-4r--V- a rida "it-vassais 9 v
P.:'A a WE 19 1 go
.f-WO 0 0_A_ 0 wo ,0.0-0 0 0 w0 & 0 4 4 0 0,0 wo 4i 6 09
I .'. .0 0 0 0 0 41-
0,6 we'.6416.64'Ce wo 0 0-0 0 04 of * 0 0 0 a 0 a * ao a & a 0 a 0 a 6, a &,& a a fj

_UzX2W?X*=A I =ddy Mad
1137R., 19661" -(In Russian], f 11
co"Olvit re- INIT W2111y. "&are 1QM
I atinumady cooled ram
low-17W (I"Stsome optimum rate (single beat-ti tmont),
then the value of the coercive force (,He) obtained is greater
than the value obtained by rapid quenching followed b
anneWing (double heat-treatment). To investigate tb~
phenotntmn, L. K, iuA N. prepared specimens in the form of
iods (3 mm.-in d1&*r W-100 mm. leng) of two series of alloys .
(1) c6ntg. 90-20 at..% Fe in the Fe-WLAJ section, and (H)
n1g. 11 32-14,aV A1L"%tt.-,O/.,,,For, each alley,
e~l
ere Z. ed I C.. half the
the '=
C
'. A,
NNW ENRON=
I Cally. For the A-NiAl series of alloj% H, lncre~wi
I
a a ly as the Fe content fell below 80 at..%, rising to a max..
. at -45 at..% Fe rqr single heatkreatment, and
of 540 Oe
7250e" at 20 at *.O/c Fe for double heat-treatment. Various
reasons are given w9y this difference cannot be due to in-
complete fleeomposition of the initial supersaturated Soln.
4nI~ vari~a linearly ~%-ith compn. (and fins the same magnitude
for fptimum single and dotible tnatments for any given alloy),
falling to zero at 6 Fe (the ~j phase), For the second
RenOR of alloys, single heat-treat-Vant gave greater values of
H, than did double treatment, &W the mm values occurred
at -24-28 at-% A]. The curres of W. for einglo-treat.
men& alloys con9g. 18-24 at.-% Al were somewhat lower than
those for the double-treatment materials. Themobservations
are explained in terms of the theories of Kittel' (Uspdhi FiL
Nauk, 1950, 41, 452) and Kondorsky (Doklady Abad. NwA
1950, 70, 215; 1950, 74, 213; M.A., 1& 600; 20,
683). H, falls below the max. valus if the d ofp"ai of the
particles of phan V. E. T.

Nd Vt N,* v.4,0.A .
ITAKOT, O*Se.; MOVIKOVA9 O.A.P; RTABOVA, G.G.
Study of the system 1ron - cobalt - nickel - aluminum, based on
the section with 50 f. 1ron. Izv,5~kt,fIx.-khIn.aml. 22:ln-139 153*
(HERA 7:3)
1. tustitut obehebey I neorgwdchoskoy khiaii ln..N.S.Kurnakova
Akademil. nauk SSM. (Iron.. cobalt - nickel - aluminum alloys)

NQTIXDVA, G,A.; RUDNITSXIY# AwAs
Irmstigating the slIver-pUtinum system. 7.hmr. noorg. khIv. 2
noo8:18406-IM7 19 057. (KMA 11:3)
(511"r) (PUtimm) (Chemical equilibrium)

78-3-3-35/47
AUTHORSs Novikovag 0. A. dnitakiy, A. A.
Investigations of the System Gold-Si-lver-Platinum
(Ionledovaniye sistemy zoloto-serebro-platina)
PIERIODICALt Zhurnal Neorganicheskoy Khim-4i, 1958,Vol-3g Ur 3,PP-729-749
(USSR)
ABSTRAM By the thermal analysis in the system gold-silver-platinuo
an m-solid solution,.enriahed with gold and silv*r,, and
an -solid solution of silver gold In platinum was do-
tormined..TheAomains of the oC- and ~-Bolid solution in
the phase diagram were determined.~The alloys were also
determined by determinations-of the microstructure, the
hrmnesso the strengtho the specific weighto the electric
resistance-as well: at the temperature coefficient of the
electric rsaistance for three-isothernal Aections at 9000
600 and 20.C0 By the6titmination of the thermoelectric
force the solubility of platinum in the ckl,-aolid solution
was determined. In alloys with 10 % silver the thermoelec-
card 1/3 tric force on addition of platinum and gold increases. On

Investigations of the System Gold-Silver-Platinum
78-3-3-35/47
further increase of the quantity of gold the thermoelectric
force further increases and at 60 % it attains its-maximun.
In alloys with 20 % silver -in an heterogeneous domain the
thermoelectric force decreases with am increase in the gold
contentg as the concentration of platinum in the vc-solid
solution decreaseso In the case,of a. constant platinum
content-and with an increase of the gold and silver content
the thermoelectric force decreases. ror the construction of
the ternary diagram binary sections with a constant silver
content were produced which stand in parallel with the gold-
-platinum side. The limit between the*4g-phase iz determined
on the basis of the analyais, of the composition diagram and
''by the nicrostracture analysis. It was found that the un-
limited solubility of gold in silver is limited by the
introduction ofthe third component, platinum. On addition
.,-of 10 % platinum the 1Z-phase-ooours in the structure of the
alloyaq enriched with gold and silver. On the basis of the
performed investigations the phase diagram of the systems
silver-gold-platinum was constructed and the properties of
the occurring phases in dependence on temperature'and com-
position were investigated. There are 23 figures, 5 tableag
Card 2/3 and 28 references, 8 of which are Soviet.

T8-3 - 3- 35/47
Investigations of the System Gold-Silver-Platinum
ASSOCIATIONt Institut metallurgii in* A. A. Baykova Akademii nauk SSSR
.(Uetallurgical Institute imeni A. A. BaykovAS USSR)
SUMITTEDs June 189 1957
Card 3/3

5(2), 18(7) SOV/78-4-7-21/44
AUTHORS. Rudnitaki-y, A. A*, Novikovat 0o A.
TITLE: Investigation of the Alloys of Silver With Ruthenium (Issledo-
vaniye splavov serebra, s ruteniyem)
PERIODICAL: Zhurnal neorganicheskoy khimii., 1959, Vol 4, Hr 7,
PP 1596-1600 (USSR)
ABSTRACT: 'In the present paper alloys are investigated which are rich in
silver* The production of alloys having a high ruthenium content
is difficult because of the diverging melting points. Ruthenium
melts only at 24450, ise. above theboiling point of 3ilver.
Alloys containing Oe59 1, 2, 3 and 5% ruthenium were investi-
gated,s All alloys crystallize by forming an eutectic at 9200,
the maximum of which is near 3% rutheniumo In the crystallizaton
of the phases with a higher ruthenium content destratification
into ~*o liquid phases occurs. First, the 0-phase, which is
richer in ruthenium, solidifies..Beoauae of the more rapid
cooling afid the inclination towards undercoolingt crystal-
lization does not develop according to the phase diagram.
Orystallizati6nLof the P-phase is not complete, and the liquid
phase solidifies with a higher ruthenium content than cor-
Card 1/2 responds to the diagram. The eutectic is formed at the end and

Investigation of the Alloys.of Silver With Ruthenium
SOY/78-4--7-21/44
fills the gapabetween the grains of the metastablo phases.
During thermal treatment the metastable phase decays, separat-
ing the P-phase. Separation takes place very sl,owly. Figure I
shows the microstruature ef the eastj and figure 3 that of the
annealed alloys* Figure 2 shows the phase diagrams of the alloys.
Table 1 gives the data of the thermal ahalysis, table 2 shows
-the mechanical properties and the electric resistance of the
alloys, and table 3 the e.n.f. of the thermocouples Ag-Pt and
alloy-Pt. There are 3 figures, 3 tables, and 4 references,
1 of which is Soviet.
SUBMITTED: April 2, 1958
Card 2/2

5(2)r 16M
AUTHORS:
TITLE:
PERIODICAL:
SOV/TB-4-7-22/44
Rudnitskiyj A. A., Novikova, 0. A.
Investigation of the Alloys of Gold With Ruthenium (Issledo-
vaniye splavoy zolota s ruteniyem)
Zhurnal neorgenicheakoy khimii* 1959, Vol 4, Nr 7,
pp'1601-1605 (USSR)
ABSTRACT: The subject mentioned in the title is refened to only once in
publication,- -L' tthe statement made by J. 0. Linde (Ref 1)
that the solubility of ruthenium in gold is negligibly lows
In the present paper gold alloys with 0-5, 1, 2 and 3~ ruthenium
were investigated. In order to facilitate a crystallization in
phase equilibrium, the alloys were kept at a temperature
slightly above the point of solidification for a considerable
time, were mixed several times, after which they were cooled
as slowly as permitted by experimental conditions. .111 alloys
were found to be biphase, the quantity of the second phase in-
creasing with an increasing concentration of the ruthenium.
Signs of non-miscibility of the two-phases have already been
detected in alloys with ig ruthenium. Figure I show3 the micro-
structure of the alloys with from 0-5 to 2% Ru. The bright
Card 1/3 phases of Rug which are not etchable by means of aqua regia,

Investigation of the Alloys,o:r Gold Vith Ruthenium
SOT/78-4-7-22/44
are irregularly distributed upon the background of the funda-
inental structure. Its distribution, shape, and dimensions show
that they have been formed in the liquid phase and that their
growth has not been hampered by anything except by the rate of
cooling, The primary secretions of the ruthenium-rich P-phase
form no crystallizatiom.centers. The melt more rich in gold
solidifies by building polymers of the solid solution, the con-
centration of which varies with temperature. Figure 2 shows
the phase diagram and ,the physical properties of Au-Ru alloys.
The results obtaineq by thermal analysis and the microstructures
lead to the conclusion.that in the system-Au - Ru the solid
a-solution of ruthenium, In gold is formed as the result of a
peritectic reaction developing at 10660. The alloy with 0-5%
Rug which is hardened at 10000 and chilled with ice water,
remains diphase (Fig 3). The electric resistance of pure Au
is hardly changed by the addition of Hu. Table I gives the
res of the alloys, figure 4 shows
crystallization temperatu
the microstructures of the annealed alloys, ani table 2 gives
;iese A consilerable part of the ruthenium phase is
their proper",
Card 2/3 separated aIt the boundaries of the laree Crains of the solid

SOV/78-4-7-22/44
Investigation of the-Alloys of Cold With-Ruthenium
a-solution in form of long; thin polyhedrons. The thermo-
electric properties of the alloys with 0-5 and 1% Ru are given
!a Bale 3. They prove the low degree of solubility of
ruthenium.in gold. The addition of 0-5~~ Ru deteriorates the
plasticity of gold, reduces tensile strength, and does not
influence hardness to any considerable extent. There are
5 figures, 3 tables, and 1 reference.
SUBMITTED: April 2, 19531 Ab3tractor'3 Note: Misprint: should read 1956
Card 3/3

00/011/011/01
9
Z021 P

Inpo-le ongat'd resistance
ion.
E Co M

RU: 2-9- 100 *C
-21

5 ~-20 5:*~~ 22.7

7 23

7- 7

a r d

w5og/62/000/011/012/019
w: - Th a': iiiflue"ne a;-. of: nxth eniuxn a 0,
no grain-
i~nd 1#-oduc ed fi -
t
_
-'t at-ur es.- theaium
Ru
s ru
-
,_ and
ins'. fi--the.-. alloys but
-d- ~iho ~hardness
.
decreased their
1 P-1 ist -a- n' -electr dal- conductivity. Them results- are tabulated.,.
er ~:T gu 1 tab e*
i roes, and;. 16
t_j ard ss' -Blimgation
Cdmpos-i
ng Olectrical

m resistanc-e,
,cm
olith

,RU Pd
Au 0 0

25 C 10i -7c;
j6
16. 2'- -3.8. 4

87' 62.0 -22 2 1710 19 2
0:2

85 79 - 1 .0

. 2
18-5
80,7:::
-a Ip
O~
18.6
16.5

:x-%~ 7'

'Investightion"'Of

sis -Bleo rica :resistancef
t
ki/aim 110hraf Cm
25 C- 100 c
00
5

-14-05-
11 .70:
-16#0 18 ob - 19-75
........
10T 4 .--15*10 17455
My
17 cO
30
8o-0

L 466oa-66 YdT(m,, /V-,!P( R14
'j Z'-P IJP'
ACC NR: Ap6oi6482 (A) SOURCE CODE: UR/0021/66/000/005/062T/0628
AUTHOR: Novikova, 0. A.; Kuznyetsova, V. N.-Kuznetsova, V. P.; Kornyev, K. A. -
Kornev, K._A-.TWrFF-esjWAding member AN Ukr6SRJ__
ORG: Institute of Chemistry of Macromolecular Compounds,,Aff UkrSSR (In stit ut
khimii visokomolekulyarnikh spoluk AN URSR)
TITLE: Polymerizat-1 riet~)rle
qnJof t thynylsilane~in the presence of (C2H,)3Al.T'C'4
as catalystri
SOURCE: AN UkrRSR.: Dopovidi, no. 5, 1966, 627-628
TOPIC TAGS: polymer, polymerization catalyst, conjugated polymer, triple bond
system, triethylethynylsilane
ABSTRACT: The article deals with the polymerization of triethylethynylsilane in
the presence of (c2H5)3 Al.TiCl4as catalyst. The resulting polymers have molecular
weight of the order of 1000, and are orange oil-like products. The infrared spectra
confirm that polymerization is effected along the triple bond system, resulting In
the formation of conjugated double bonds products. (Translation of authors' abstrac
(AM)
SUB CODE: OV SUBM DATE: 13Nay651 ORIG REF: 005/ OTH REF: 003
Card 111 mjs

LYUBIMVA, W.V. doktor skon. nai*,- -KOMMITA,~afis-kand. ekon. nauk;
A.G... kand. skon. nauk; IVANDV,, X.P.,, kand. istor.
-nmik; OBDRMi G.A.,, kand. ekon.-nam4_KHLYXOV, V.M., kwA.
MAp daktorsken. nauk; POKATAUTAI
T.S. j kqdC ekoho nauki USOV, G.A. 04and. _ ist. im4;
SALf KOVSKIYj~ 0. V. t, kand. . geogr, nauk, Prinimali achastlyst
MORIMS..IY,.. V V. , kand. ist. nauk; PIWWVA, I.M.; PROMIN,
S"V.--USVYATSOV. A Yea; MAKABOVq,V.F,r4d.,; DAROMN, K~I,
I V ~ ~ ~4
;;Xhly teC; ULMVAq L.1, tekhn. red.-
lReal.wages during-the period of.th& general crisis of capt-
talism]Rmalinals, sarabotnaia plata v period obshch6go krizisa
kapita lisma. Moskya, Sotsekgis, 1962. 559 P. (MIRA 16:3)
1. Akad nauk SSSR. Institut mirovoy ekonomiki i mxhdu-
body.
(Wages)

NOVIKOT&ON&IWelelfthly umchnyy sotrudgLik
Calou2stica Of TOUCHY pOtentials MA flow veloolties about annular
cascrAss. with high volIdIties. ITMAYI TSUI no*-27:52-58 154.
(Gas f low) (mm 8:12)

ZHUROMIt-M.I., doktor tekhn.nau-k; SINARI, N.A.#, kand.t4khn.nauk;
GWLASOVAj, TeA., inah.; MIKHAILOYA, V.A., iizh.; NOVIKOVA, 0.1., inzh.
Aerodynamic -characteristics of blade profile lattices of"the
terminal stages of X-300-240-IM turbines. 'Energow hinostr;onis
8 no.10:29-33 0 162. (MM 15:21)
(Steam turbines)

ZRUKOVSKIY, K.I.,, dektor tekhn.nauk; NOVIKOVA, 0.1., inzh.; qKNARI,, N.A.,
kand.tekhn,nauk
Dmaing method mid experimental de"lopment, of a group of guide
blade profiles with incres"d values of the moments of resistance.
Thploonargetika 9 no.10852-55 0 162. OIRA 15:9)
L. T.Sentral-layy ketloturbinnyy institut.
(Turbines--Blades)

DURAKOVv N.I., Inzb.; NOVIKOVA, O.r.,, inzb.
Calculations of an axleymetriial flow In tho blad-Ing of to
axial-flow blover using electrmic calculating maehIns3.
Teploonergetna 10 noelOt35-38 Ot63 (MIRA 1797)
1. TSentrallnyy kotloturbirmn Instituto

A~-""EZIUN XR1 AP5005264 3/0291/64/000/t)06/0061/0066
I-
IL)
.~JTHDRS: Novikova 0. S.; Rassonekaya, 1. 3.; Rya4ova, ii. D.
1-3
TITLEi Thermographic investigation of SOMC. Syrnthebic Mat."
WUFCL. Uzbekskiy khImicheskiy zhiirnal, no. 6, 1964, 61-66
TOP:.-C TADS: themographic ariaj-yais, x raq analyLls, zoo"lite/ Kurnakov pyrometer
AMMACTs This paper Is concerned witch rhenria--, treatatent, thermal stability, and
aen~j-d.~~-atiDn of zeolites. A large series of zeolibes vere examined by being first
e2h hours.
at constant weigbt in a desiccator over a
I -!CJ'U' 3olution of H2304 for
Vhe-:-nal cuxves were obtained c-a a Kurnakov p-:-romet.r.,r '-seecLmen wei&ht of 0.6 g).
All thermograms shwed a

AC(;K-MON NRI AP5oo5264
de!izIration of zoolites ma7 be reached by heating to 500C. The most rapid
~-~i.mination of water takes place in tha ;Interval Greatest capacity
IUX
w;~~ obrw-vod in 'Nal (29%). CaY (29.2%). 1.44 (29.03%), and 14 (29.3%) . Thf3
iaLlqvt capacity was f ouW in CaA Orig. art. has t It f lgitrea and 2
t
"'ab 1 e 8
A-SS(XLATION: Institut khimii W4 Uz-53P (Institute of Chemi-st
I - 1-1 _4 ~1- K7 Q A~AO.Dakrr-,

NolrmovA, O.m.; SATTAROV, I.S.; BELYAYEV, L.A.
Epidemiological and clinical characteristics of pertussis-like
dix-eases caused by Bordetella, parapertussis. Zhur.mikrobiol..'
epid. i immuno 42 no*4:1.26-131 Ap 165. (MIRA 18:5)
1. Ministerstva zdravookhranenlya SSSR i Institut epidemiologii
i mlkrobiolog~i imeni Gamalei AMN SSSA

NOVIKOVA-C.S.; RASSONSKAYA, 1.3,; RYABOVA, N.D.
Thermographic investigation of some synthetic zerlitee. Uzb, khim.
zhL,--. 8 no.6361-66 t64. (MIRA 18:4)
1. Institut khimii AN UzSSR i InaUtut obshchey i neorganicheskoy
lehijali Imeni Kurriakova AN SSSR.

RASSOIISKAYA, I.S.; NOVIKOVA, O.S.
Dehydmtion of crystal hydrates of disubstituted ragnesium
phosphate. Zhur. neorg. khim. 10 no.6:1423-W6 Je 165.
(14IRA 18:6)
1. Institut obshchey i neorganicheskoy khimil imeni Kurnakova
AN SSSR.

NOVIKOVA, O.Si,; ADYLOVA, T.T.; IffABOVA, N.D.
Using the differential thermal analysio data for the ebaracteri-
zation, of mineral adsorbents. Uzb.khim.zhur. 8 no.4s43-46 t64.
(MIRA 18:12)

GOLUSHKO, N.A.; ALE&UNDROVA, T.A.; FROKHOROVA, I.Ya.; NOVIKOVA,, O.V.
__.- ...
Graphite-containing cruciblas. Ogneupory 29 no.1:5-U 164.
04IRA 17:3)
1. Luzbakiy zavod "Krasnyy Tigell" (for Golushko). 2. Vsesoyuznyy
institut ogneuporov (for Aleksandrovap Prokhorova,, Novikova).

A
I I-.- I I

0 0 0 0 0 0
L: ja jr
E_J~ AL A -,g- 4--c-L, S6--A-J-- t _IE~ L~ L_L_4_~71
k jo ls~.40,p ms
00 -
A On Ow'hr AN dw CqOn Id dw
llppmlllllkl~ Ind U. V. Savestpu4m.
0_0 -atign); cum. zc,*.
low. 0, WA-S.-CAMCOWS. FOOD a" und as a fifter for
dw Wrored. The bw cvmdts mtre obtained with an FcO
-4 min.
of 0.33% of lk glam ol.1
Tfw imusparrmy to radiations 44 various rt-Siom at the
Spectrum =d the undtiflicyof the titter were teled with
both natural &W xnWK4&1 sunkht. It. G. Mwcc
1. 10 OCTAWW' OCAI, WIEWIMV CLAINMCATICO
-a -1.1" 40 eel$
#&&lairw 4mv All
a
U 9S..&W ID is[, It
0 0 Iv IV 10 9 K 9 41,19 X.All
too
Goo
moo
goo
GOO
dG*
see
see

live
P.
I lit
19 ~A Rai
'low
Im
triag.111
ILI 41 it I
tic
t P lit
Millitt
fill

AC%; A-17002121,.
~AUTHORS; Novikovai-q:'V.; Hozanov, N. S.
OIRG: none
-TIM; A study of'the stressed state of hydrotechnical pressure tunnels
SOMCE: VsesoyUZnaya konferentsiya: po polyarizatsionno-optichesk6ma metodu
i5sledovaniya nap :azheniy- 5th, Leningrad, 1964- Polyarizatsionno-opticheskiy metod
ry
issledovaniya napryazheniy (Polarizing-optical method of investigating stresses);
trudy konferentsii, Leningrad, Izd-vo Leningr. univ., 1966, 433-444
TOPIC TAGS: hy, draulics, material strength, dam, stress analysis, concrete
ABSTRACT: The results of an experimental study of Ithe stressed state of the jacketing!
in underwater tunnels of the Aswan Dam (United Arab Republic) are presented. The
studies viere conducted with the use of the polarization-optical method. The '.,I=els
have different outlines at various sections, and are strengthened by concrete jacket-
ine 1-4 m thick. In certain instaLces the surrounding mass of the dam is cement-
strengthened to a depth of 7 m. The stiffness of the materials at various sections is
characterized by their deformation modulus Eg taken to be equal to 2.0-10-2.4-10
k,-,/cm2 for concrete jacketing, and 0.25-1o5-1-5-io5 k,-,/cm2 for respective parts or
the dam. During use$ the tunnels undergo hydrostatic supply water pressure heads up.
to 100 m. Such presoure may also occur in the clearances between the Jackoting and

PETROV.. 7.A.; 9SIPOV, I.S.; FIVANOVA, P.S.; MOVIKOVAj R.K.
Relation-of the surface qose distribution in -off
:9", T 1640
to~-,th*4tate of collimation. Med. rad. 9 no 2.,
17:9)
1e TSentrallnyy nauchno-issledovatel'skly institut'.6odiiiinskoy
radioloei-(dir. Ye.I. Voroblyev) Mini sterstva %drm"okhraneniya

,NOVk~G.VA, ~ppirantu
. ......
Clinical symptoms in experimental trichomoniasis of swine.
Vaterirarila 41 no.9s62-64 9 164. (IaRA 18-.4)
1. Vitebakiy veterinarnyy institut.

NOVI KOVAAalw; - - ---
Anesthesia in thymectow( for malignant myasthenia. Eksper. kbir. i
anest. 9 no.1:73-74 Ja-F 164. (MIRA 17:12)
1. Kafedra fakulftetakoy khirurgii (zave - pror. KeT.Ovnatanyan)
Donetskago meditsinskogo Instituta (dir, - dotsent A.MoGanichkin) na
baze oblastnoy bollnitsy (glavnyy vrach M.Zubko).

M V~
'ACCESS= NRI AP4032638 A/0903/dh/WWd02/0333/03U
~AUMORS; Bobrovj, He S.; KGr*lWft# N. F.) No*fJkCV&p He He
~TXTLZZ Properties of the solar wind dwordiag to pacmasat gempetia astubsA44
on days with v*x7 law 11P
SMUEs Gsomagnatl= L asronomiyas v. 4* no. 28 1964j, 333-341
TOPIC TAGS: solar windp geomapetic disturbance, coryuscular stresm, polar caps
Mariner 20 F)?
;ABSTRACT.- Initial data for this study were the hmwly amplitudes of the H
,component of magnetic disturbances recorded at observatories on the northern and
!southera polar caps during days of very 2aw planetar7 magnetic wtivity. The
.investigated interval waa from July 195T to D4cember 1962,, Days ot law activity
.were considered to be those in wh4ch Kp and the daily total 11~ did not exceed 20
'and 100 respective2ye The authors have shown that the disturbances were due to tho.
:solar wind, An analysis of the disturbances indicated that for the parind Investi.
-gated the solar wind was permawt with respect to tims, It repress&W an
card 1/2 .... .....

BOBROV, M.S.;JIIT~IKOVA, R.T.
Relationship between the solar corpusd%Ur wind intensity and
the phase of the solar oycle. Astron.tsir. no.242:1-2 Yq 164.
(MIFA 17:4)
1. Astronmicheskiy sovet AN SSM.

-4
14, /E 7C t W -4 h
~-6
A A F 7' 7: Z. W F
A-11CUSION MRi "4038682
SOMONs Rat, Sho Astron, ft4- TrPes Abu, 3#51-420
A117110M Bo
TITIM Dependence of the intensity of the Fjolar aorpusoAlar q
jz4 or t. a of
e')lrlr nativity qq pbs"
- ---- -- ---
S.OMU-A~~cku* tairkulyar, no, 242(MV& 4),, 1963j, 1-2
TOPIC TAGSt astrophysics,, volar antivity, aol,3r aorpu9oular wdnd, roomagnetio
N-31d, gemAgmstio disturbwice
'100SLAT1014i Using ths period frm July 057 w-ithorti ha"
-.he mean lossraal -ftdul~~ .-~f th~-N ho~2r;y ~-he horilmmt4l oum-
c n (I n t n r t h ~ 27 e emn gm a ti n f 1 6 14, 'A i r n ~n, An'3 Yl q I

:-A, 7 77-
:DM IJCQI liripvka
SM CODIs M, AA
VCLs 00

(A
ARKRUGHLI~~.'KePe, kmdldat takhnicheskikh nauk;NCWIMA. S.A..
P.r., imzhe"T.
$pal" method of determining - lrrqp2arit Is@ In dyeing wisce"
rayon. Idmt.prm. ii no.n:40-41 1 155. (KZU 9:1)
(Dyes and 4yolmg-layou)

- NOVIKOTA,# 8,L; VOROBOIRVAP V*l*
lacroscopic studies of dyed cross sections of viscose fibers.
Rhimovolok. no*3951-53 -64, (MIRA 17:8)
L VeasoyuzMy nauchno-iseledovatellskiy inatitut iskasstvannogo
voloknas

DWINA, Natallya Vasillyevna; NICTORINA, Aleksandra Vasillyevna;
IIOVIKOV, Nikolay Alekseyevich., kand.tekhn.nauk;
NIOVIKOVA, Sofiya Aleksardrovna; LEYCh-E-11KO, Eleonora
e dW'."--W-AI9!V'~?ABFILOVA Mariya,
MMaylovna; ROGOVINA, Alias. Aleksandrovna, kand. tekhn.
nauk; RWIAIIOVA, Lyubov' Stepanovna; TALYZIN, M.D., kand.
tekhn. nauk, retsenzent; VERBITSKAYA, Ye.M., red.
(Methods of physicomechanical testing of synthetic fibers,
threads and films] Metody fiziko-mekhanicheskikh ispytanii
khimicheskikh volokon, nitei i plenok, Moskvaq Lagkaia
industriia., 1964. 352 p. (MIRA 18:1)
1. Vsesoj-uznyy nauchno-issledovatellskiy institut iskus-
stvennykh volokon (for all except Talyzin, VerVtskaya).

ROGOVINA, A.A.; NOVIKOVA, S.A.; GILIMAN, I.S.; VASILIYEV, Yu.V.
.Some structural changes in polymmide fibers ocmwr.'Jr;g dwing
heating and dynamic fatigueo Khim, volok, no,4:56-60 164.
(MIRA 18%4)
1, Vsesoyusnyy nauchno-issladovatellskiy inatitut takusshrennogo
volckna (for Rogovina, Novikova). 2. Moskovskiy tekstilinyy
institut (for Giltman, Vasillyev.).

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MVINS'rA. L. Yu.;, NOVIKOVA, S. 1.
Serological proportion of secondary phagorasistaat cultures of
Str. lactim. Mikroblol. shur. 16 no.l-.48-53 154 CHM 8-4)
1. Z Institutu m1krobiologil AN MM.
(STIVTOCOCCUS.
lactis, serol. properties of phago-resist. strains)

MEDVINSUrA, L.Tu.; MOVIKOVA. S.I.
ftes of lactLo acid stmptococal bacterLophap. Report K*.3L:
ObtalnUW *as of lactic acid streptacceeL bacterLophegs and their
chareqteri stices Mrobiolexhur. 16 no.4:52-57 f54. (MM 10:1)
le 2 Institutu nikrobiologii Akedenii nank URM.
(BACUSIOMO) (IACTIC ACID HACTUIA)

thL, ini cy~j~
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1. Nov ova. AY47gbridif. Zktjr.. 't
Mouk im. D. X~ ZU646marg
11, No. 2, 41-hMuvslan wtumary, 401,0W).-Ruh6a
Sud Novikava (Cl. fou"ing abstr.) Showied !hat .3. laclis
Vown in aft in the presence of luietwe uoizeA ititrg. P
A#, ANO the frW" at enoy k5l4tolylt'i P t"3 incrtas"I
It vM WAumed that thz 6witastj Ir. Oi~ fmatinn ucv.'r.'ril t
the exqma of the faruiagtwi 4 S-gw'uvt%Ke
T
and at-glucattim-p"pluift 6N, lmlicacing thut thr-e -iiUS
men jp~gtdiaxy pmPxeto of tit, procega of jact.3c fdr-
S. ilactir. An attempt was maile to check
Ou d*=00itnem of this as.!,umptiun. I and H were sui>-
1=04*1t4e actiou of-wasbcd culturts of S. iocttu and of azu.
eeiW. Neither the livin Nwtelial nor
Unit Ii attacked 1, ve r1
-hich i--; the pro uct oi dh x( phi:5-
w0f. ltwto-e - I t was c"(1clud ed tha t I "U I'll Out be
phosj&t-
reprdj4jW it produv if lactiAc (ei-rnentafian by S. lactm
that 3~ kulu dt.,es vijt ihril-oiyze kicnric by wt~y
dirtct phtephorylatloij. 1-he witsbed cells -,,i 3 ~ricnj
actively ferml-"Itcd 11, hydrolyxif'4 in lia-tw ci:!.
..U It"ta. cil" -.'ertcd 11 Into ~;'w hydri,syzed P
eatem gluc"'~*" 5~phospiratfi.' that ul these exl~-
ph-Phomutuse was pre.,-evt. It Eq Conelit';t"I th-at glu-
,ose phosphate ~,-vd Kluui~r jzitvr-
mediary prod"ts of tit,- J lnrt-~ u)
S, l4clij. 1-vine