SCIENTIFIC ABSTRACT KUZNETSOVA, G. P. - KUZNETSOVA, I. K.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R000928220005-3
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: June 20, 2000
• Sequence Number: 5
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

POKROVSKAYA, L.I.; PLYUSUCHEV, V. Ye.; KURIFTSOVA, G.P.
Study of the system lithium sulfate-cesium sulfate -water. Izv.
vys. ucheb. zav., khim. i khim. tekh. 7 no.5:705-710 '('-
(MIRA 18:1)
1. Kafedra khimii i tekhnologli redkikh i rasseyannykh ele-
mentov Moskovskogo instituta tonkoy khimicheakoy tekhnologii
Imeni M.V. Lcmonosovae

"of rare

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PLYUSHCHIEvr, V.Yp.; SIIKIOVFR, L.P.; SHKOLINIKOVA, L.M.; F!j7*;N-E-,bOVA, G.P.;
IMUSIJ TNA T.A.
~ .9
Yttrhim and erbiiun formates and the"r propertAlpl. Zhur. ob.
khint. 35 no.lOtl783-1790 0 '65. (MRA 18;10)

KUZNETSOVA,,P~.~.; STEPIN, B.D,
System at RbBrF-IlBr - H20 at 250C, Zhur. neorg. khim, 10
no.2s472-475 65. (MIRA 18tll)
1. Vo&ooyu%nyy nauchno-iseledovatellskly institut khirallcheakikh
reektivov i osobo chistykh khialchaskikh veshcheaty. Submitted
Aug. 24s 1963#

-kVr4IETSOU,.S,P.; SIIVARTSp M.M.1 STEPIN, B.D.
Preparation of highly pure sodium and potansium monochromates.
Izv. AN SSSR. Neorge mat. 1 no.11:1938-19" N 165o
(MIRA 18:12)
1. Voesoyuznyy nauchno-iosledovatellskiy institut khimicheBkikh
reaktivoy i oBoboohistykh khimicheakikb veshchastv. Submitted
May 14, 1965.

BALANDINA, V.A,j XLESHCHEVA.. M,8,j XUZHETSOVA 0.3,; TURKOVA, L.D.
~ ,
Quantitative evaluation of chromatograms with the aid of a
detector of heat conductivity. Zhur,anal,khim. 18 no.7:808-
810 Jl 163, 1(14JAA 16 M)
f
1. Scientific-Research Institute of PolymerizationIklantics
and Experimental Plant) Leningrade I

KARIAKIN, R.N.; PUPYNIN, V.N., kand.tekhn.nauk; KUZNETSOVA, G.S., inzh.
Experimental investigation of the ourrent drain circuit of a.c.
traction substations. Vest.TSNII MPS 22 no.022-25 16).
(WRA 16:10)

KARYAM, R.N., Y_!,nd.tekhn.nauk (1,1,()-kva); KUZNPJ~~GVA linzil. (!-;c1jyV[1)_
FUMIM VA.? MIT rfF f?. ~nz",.
kand.tekhrl.r,auk (MrsW~;O_j7 P P
Be le c LIon of effective networka and optimal paramotxra of t1he
power take-off circuits of a.c. traction substAtions. E1ekfrichs.,f3tvo
no.11:10-18 N 164. (HIRA 18.2)

KUZNETSOVA, G.S., inzhs
Experimental study of the thermal stability of grounding systems.
Trudy WIT no.199:165-177 165-
(MIRA 18:8)

Puiyrflfilp VeN., dQtrant, kand.tekhn,nauk; KULNI,"TSOVA, G.S., Inzh.
Appro-yimate evaluation of the thermal stability of the grounding
stages of a.c. traction substations& Trudy MITT no.199.178m-183
165. (KRA IW)

NOVOOMHOHENOVAp N.S.; XMNMCNA O.S.
1--l-1-- - -
Characteristics of the flea ecology of groater gerbils in
places with chronic plague spizooty. Zool. zhur. 43 no.Ils
1638-1648 164. (MIRA 18%n)
le VseooyumVy nauchno-UsledoTatellskiy protivachumnyy
institut *Hikrob*,, Saratoy.

BALANDINA, V.A.; KLESHCHEVA, M.S.; XUZNETSOVA, G.S.
Determination of the composition of a mixture of acetaldebyde,
methanol,, and vinyl acetate with the aid of gas-liquid partition
chromatography, Plast.masey no.?f6l-62 163. (MIRA 16:8)
(Aestaldshyde) (Vinyl acetate) (Gas chromatography) ~

TSIRL.M. Yu.A.; VASIMYEVA, V.A.; KUMETSOVA, G.S.
Chemical purIfication of sewage containing furfurole. Oldroliz.
I loookbim. prom. 14 no.7:15-10' 161. (MIRA 14ill)
1. Nauchno-looledovatel'okly institut gidro]Aznoy i oullfitno-
spirtovoy pramyBhlennoetl.
Sewage.-Purification)
traldehyde)

F-,-U -r- (,u
Hall"

FZTROV. A.A.; BRAVO, Ye.S.; DAVIDOVICH, V.V.; DYATKOVA, O.S.; KMBTSOVA G.V.
Investigations In the field of conjugated systems. Part 49. Order of
adding alkyl hypohalides to tertiary vinylaostylene alcohols. Zhur.ob.
khim. 23 no.7:1120-11,24 J1 153. (KLH& 6:7)
1. laboratoriya organioheskoy khImii Leningradekogo tekhnologicheekogo
institute. imeni Zensovata. (Halides) (Vinylacetylons alcohol)

PLLIINIK, R.Ya.; 'VlP',`!i4,,4., i,1,
Formation and -structure cf the
r ur;
neglectum Ldb. Trudy TSSIJI; no.7v-)f~44,

S/169/61/000/011/058/065
D228/D304
AUTHORS: Kuznet and Soboleva, N.S.
TITLE: Observations of solar radio-emisBion by means of the
Bollshoy Pulkovskiy Radiotelescope in May 1960 on the
8.7 cm wavelength
PERIODICAL: Referativnyy zhurnalp Geofizika, no. 11, 1961, 10,
abstract 11G87 (Solnechnyye dannyye, no. 3p 1961p
70 - 72)
TEXT:' The observational procedure is described. The end of the ra-
dio-emission splash was recorded during the observations (at 9 hr.
55 min.). The chromospheric flare connected with this radio-emis-
sion splash had a force of 3+ and lasted from 5 hr. 22 min, -to 7 hrl
33 min. world time. The radio-emission splash was also detected by
the Glavnaya astronomicheskays. observatoriya (Central Astronomic
Observatory) radiotelescope (3 cm). An estimate is given for the
flow, size, and temperature of the evolutional brightness which was
still preserved after the splash. [Abatractoi~s note: Complete trans-
lation).
Card 1/1

379h2
S/035/62/000/005/037/098
A055/A1O1
.1,172.0
AUTHORS: --Kuznetsova. G. Y., Pariyakiy, Yu. N., Soboleva, N. S., Khanberdyyev,
TITM; Observations of solar radio emission during the eclipse of February
15, 1961, on the 9-am wavelength
PERIODICAL: Referativnyy zhurnal, Astronomiya I Geodeziya, no. 5, 1962, 42,
abstract 5A326 ("Solnechnyye dannyye", 1961,'no. 4, 65-67)
TEXT: The results of observations of the solar eclipse of February 15,
1961, are described. The observations were carried out with the
aid of a paraboloid(D - 4 m) with azimuthal mounting. The open end of a round
waveguide. Into which were inserted a quarter-wave plate and a ferrite modulator
with 30 cps modulation frequency, was used as primary exciter. The half-power
0 . -travelin&rwave-
directional pattern was 1.5 As radiometer, was used a three
tube strgight amplification receiver with an equivalent input noise temperature
of 4,500 K and with a'passband of 300 Mc. The circularly polarized component of
the radio emission and the nonpolarized radiation of the Sun were recorded. The
recording wan effected on an 3nn-og (EPP-09). The antenna temperature of the
Card 1/2

S/035/62/000/005/037/098
Observations of solar radio emission ... A055/AlOl-
Sun outside of the eclipse was 5,5000K. The Moon was used for the absolute 22
calibration. The flux from the Sun on the day of the eclipse was 125 ' 10-
watt/m2cps. The opening of the coronal condensation from 8hl7mIn .5 to 8h2omin
(universal time) was ascertained from the examination of the eclipse curve.
Under the assumption thai the source has a round shape (D.1-1!2) and that the
condensation has the shape of an ellipse with semiaxes 0. x 1!14, the brigbt.
ness temperature was calculated and proved to be 3.1 - 1090K and 2.75 - '10 K
respectively; i.e. it proved to be higher than the temperature of the undistuib-
ed corona. No polarization of radiation from the condensation was detected,
which is indicative of a sharp directivity of the polarized radiation, this
directivity being related to the radial direction of the magnetic field over the
spots. The residual flux during the maximum phase of the eclipse was 40 - 50%.
M. Gorelova
[Abstracter's note: Complete translation]
Card 2/2

30426
B11091611006101210011020
/7// CIIA7) D266/11305
AUTHORS: Yesepkinap N.A., Kaydanovskiy; N.L.1,Kuzneteov, B.G.,
.Kuznetoovap GoVel and Khaykin, S.E.
..... .................... .
TITLE: Investigating the radiation pattern of highly direc-
tive antennas whose reflecting surface is adjustable
PERIODICAL: Radiotekhnika I elektronika, v. 6, no. 12, 1961,
1947 - 1960
TEM The purpose of the paper is to derive mathematical expressi-
ons for the radiation pattern and for the effective area of a cer-
tain class of antennas. The antenna investigated consists of a lar-
ge number of elements (rectangular metal plates of heieht h and
width a) whose position and inclination are adjustable. The elements
are in no mechanical contact with each other which facilitates grea-
ter accuracy of manufacturing. They can be adjusted in such a way
that the main lobe of the vertical radiation pattern is in a speci-
fied direction (8 . in Fig. 1). This condition Is satisfied if the
radius vector of the center of the elements is given by The follow-
Card 1/#

3U426
8/109/61/UU6/UI2/001/020
Investigating the radiation pattern off D266/D305
ing formula
P P R0 - a0 Cos go
1 + Cos 00 COST 1 + Cos go -008 q
where p constantp T - angle between the radius vector and the x
axis (see Fig. 1) , If 0 ---- 6 0-< St/2 (1) represents an ellipsey for
80 = 0 a parabola# and for 0 0 = IT/2 a oircle. It follows from (1)
that the distance between the primary source and the reflector de-
pends also on 0 0. The inclination of the metal plates is determined
by the angles p and X (see Fig. 1) which are related to e 0 and
as follows
sin gin go (3)
+ Coe 00 Gas rp)
and t an X 811a ce (4)
COB 00 + cog re
Oard 2/4-~

Investigating the radiation pattern
S/109/61/uu6/Oi2/OU1/020
D266/D305
In a plane perpendicular to the direction of the main Lobe, the
waves are in phase (this ujust be always the case because the an-
tenna was designed according To -this criterion) and the shape of
the illuminated area in this plane is an incomplete ring. The dis-
tribution of the electric field kboth poiarizations are present)
in the aperture is calculated by geometrical optics and The far
field is obtained with the aid of viave optics. The arising inte-
grals are in-ceerated out leading to an infinite series of Bessel
functions of the lirst kind. The radiation pattern is calcuiated
for the reflector current as well. No analytical solutions are
found in this case, out some numerical calcu.Lations indicnte simi-
iar results to Lhose obtained by the aperture nethod. Aperture ef-
riciency is also determined and wonotonically decreasing function
of 0 0 is found. in conclusion the authors express their 6ratitude
to V-13. i3raude for his assistance. There are 15 figures and 9 re-
ferences: 8 6oviet-bloc and I non-6oviet-bloc. The reference to
the B~nglish-language publication reads as foilovis: :3. silver, mi-
crowave Antenna Theory and Design, m.I.T. Had. Lab. zierics.
SUBMITTED: February 22, 1961
Car(I 3/4

!qJ-ZNET3QVA,-G.V.; S-30BOUNA, N.S.
Polarization measuremonts with an antenna with a variable profile
reflector. Izv. GAO 23 no.3:122-127 1(1,.
(MIRA 17:11)

PETRUNIKIN, V.Yu.; YESEPKINA, N.A.; ~F~IFETSOVA, G.V.; MIZUETSOV, B.G.
Effect of rotation of the principal crons Bections of the
directivity diagram of an antenna with a variable-profile
reflector. Izv. GAO 23 no.3:160-161 164.
(MIRA 17:11)

___Tj
ACC _Nxj SOW= COMS
AUTHCRt Xelfaikovo Me Net H-uridshAMB. Ke A2; K=111stsova. Go Vt; gunn-
ORG: All-Union Scientific Research Institute of-Chemical Aents of Plant Protectil
Xoscow (V8eaq_y__u-%nyy nauchno--Isoledovatolvskiy Inatitut khImicheakikh aredstvMM
rasteniy)
MIES Herbicide~arvd plant growth regulators. XLII . Synthesis of chloramethyl-
arylw-alphazp_~ionic and chloromethylaryloxy-gana-butyric acids
SOURCE: Zhurnal organichaskoy khimii, Y. lp no. 12, 19658 2166-2169
TOPIC TAGSt plant growth,, herbicide# chemical synthesis,, carboxylic acid, methyla:
chemical reduction, Mar &mine
ABSTRACTS Study 0 6jjrr'oj;vthyUtjm of arylox7a2kylearbo3wlic acids
-has shown that in &21 cases the gorrespowurg Gh1or*mtVUry2*jW&lky1_
cav~box7lio &oide a" prodWed In pod JUM4 MA the rwtift 00=0 lullder
rolativoly n11A oonditionve TM chlormet1W). gmp entmg povj+Ao3% 4, but
'it position 4 Is fIlled, It entors position 2. %1~ course, of the reaction
Is domonstrated by the fact that In tbos redu4tim of ehUramthyl derivativas
tho corroxporA4ng matIVI dwivauves described in the Uterature are obtainods
For examples reduction of the prodmt obtained by oblorameWlation of 4.
chlorophwoxy-gomma xxtyrin acids reaUto in 4-ohlaro-Zwoethyl-phenoxy-gamu-
butyrio &OAd. StV4 of the pbpioj0gjQ&j &GUdty of the ocapowAs synthesized
abows that eb1ar6*sthAA*UKPM.&-#___WUo ac"s Gro 1"s to3d to Plants
than the oorrespondim &rY2WW"42G&rboX*-Uo saidae Th find now compounds
physiologicaw seuve fW plabut weral 2074"tkd&X7163W&W1"rbox;y1iG 1
acids 0 UAL 4 odk In us utecata" wwo wPosizods.
urge art* hast
%ffi a 001
SUB C 06 / SM DAM 30 __MG RIW:
M~ IM, 22 3

MKINIXOV, IRIIIIII)ZHANYAN, F.A.; L.P.
ilerbAcIdes and growth promoLing substances. Part 43.6 Synthesis
of chloromethylaryloxy- o~-propionic and chlormathyl-aryloxy-
V%-butyrio acids. '"bur* org, khlm,, 1 not 120166-21.69 D 165
0
(MIRA 19t1)
1. rbasoyuznyy naucluio-issledovatellak3y InsLitut khlmlche--k:Lkb
sredstv vanhchity rasteniy, Moskva. Suhn-ittq5d Novembor 10,
lgfd,.

KUZNETSOVAp Ids Aleksandrovna
Changeableness of Forms and Structures of the Famw and Applied
Significance
Dissertation for candidate of a Medical Science degree, Chair of Normal
Anator#W (headj Prof, V.I, Bik) Saratov Medical Institute, 195h

KnMSOVA,I.A.
0 &a n wilpose tissue in relation to the photoperodic reaction
and diapause of insects. Scol.shur. 34 n0-3:532-541 vq-je 155.
(KU1 8:8)
1. Wedra antomalogii Loningradekogo gasudarstyeanogo universiteta
im. A.A.Zhdanava.
(Insects--Physiology) (Adipose tissues),

I. A.
Kuznetsova, 1. A. -- "The Biology of the Black Pine Beetle in the Fores-
ted Fepirms near the Steppe in Connection with the Development of
Measures to Combat it." All-Union Order of Lenin Academy of A'Igri-
cultural Sciences imeni V. 1. Lenin. All-Union Sci Fes Inst of
Mant Conservation. Leningrad, 1956 (Dissertation for the Degree
of Candidate in Biological Science)
Fot Knizhnaya Letopist No 1,~, 1956

/ , 1 -//7. /_1
1~r r
USSFVGonoral and Systematic Zoology. Insects. Harmful
;naects and Acarids. Forest Posts
Abs Jour Ref Zhur - Biol., No 3, 1959', No 11657
Author Kyznetsqyi~~_.I-A,
Inst A1r--UEf6n Institute for the Protection of Plants*
Title i Biology of the Larvae of the Black Long-Horned
Beetle,
Orig Pub i Tr&' Vaes. in-ta zashchity rast,, 1957, vyp. 80
75,688
Abstract t Investigations were conducted in the Saval foros-
try. The long-horned beetle Monochamus gallo-
provinicalls bears a one-year jeneration; however,
in a portion of the population a larvae (L), the
diapause (D) stretches out to 2 and 3 years. The
characteristics of the 1-year-old and 2-year-old
L are presented, The numbers of the diapausi%
Card 1/3
USSR/Gdnoral and Systematic Zoology, Insects. Harmful P
Insects an4.Acarids. Foroat Posts.
Abs Jour Rof Zhur - Biol., No 3, 1959, No 11657
L increase sharply in old dying-out nidi; this
is connected with drying of the trees as a result
of their tops being defoliated by the beetles.
Prior to pupation, the beetles feed during April
on decayed bast fibers and sapwood, crawling out
for this purpose from passages under the bark.
L. remaining in the D state during the spring per-
iod, are distinguished from the individuals feed-
Ing after hibernation by the Intensity of breath-
ing, the character of metabolism and the quantity
of water and fat in the organism. A low-breathing
coefficient and profound changes In the structure
of the tissues, confirming the prouonoo of D In L,
are peculiar to them, The effect of deep D on the
Increase of the beetle reserve in separate years
Card 2/3 - 41 -

KUZNETSOVA, I.A.
Possibilities for acallmatizing local ecologic races of Lapidoptera
in other zones of the range of the species. Vop. ekol. 7t89-91
1624, (mikk 160)
1. Leningradakiy gosudaretyannyy univerBitet.
(Leningrad Provinoe-Lepidopter'a) (Acclilr4izatign)

-KMLITM-t-~-
Factors causirg the begiming of the diapause in the mal2ow
moth Pectinophora malvena Hb* (lepidoptera,, Gelachiidae).
&to oboar, 41 no,31510-515 162o (MIIU 15:10)
1. Biologicheskiy institut lan3ngradskogo.gasuderstvennogo
universitetat Staryy_potergofs
(Goloohiidael (Diapause)

LEBEDEVA, M.N.; KUZIIWfSOVA, I.A.
Pharmacology of the preparation hexachloroparaxylenes Mod.
paraz. i paraz. bol. 32 no.6t691-696 N-D 163 (NIRA 18:1)
1, Iz laboratorii farmakologii (zav. V.F. Gladkikh) otdela
gellmintologii (zav. - prof. V.P. Pod'Iyapollskaya) Instituta
meditsinskoy parazitologii i tropicheskoy meditsiny imeni
Ye.I.Martsinovskogo (direktor - prof. P.G. Sergiye-w) Mini-
sterstva zdravookhraneniya SSSH.

ZKVINA, G.B*; KUZNETSOVA, I&A,-, STAROSTIN, I.V.
Compoeition of foullng in the Gaspian Sea. Trudy Inst, okean.
700-25 163# (MIRA 17:7)

TATEEVOSIYAN, Georgiy Ovanesovich; KUZNETSOVA -I,,9,,,-nauchnyy red.;
BDNDAROVSKAYAO G.V., red. ZLOVSKAYAg M.D.0 tekhn. red.;
PERSONt M.N.# tokhn. red.
[Presser of plastics] PresBovshchik plastmaes. Moskva, 1~en.
uohebno-pedagog, ltd-vo Proftakhizdat, 1961, 318 p.
(MIRA 15W
(Plastica-Molding)

7-UTEVOSIXAN, GOO.; XUZNETSOVA, I.B.
lYete=ining the photontability of coloro of plastics. Pjastmassy
no,l2t54-57 161, (HM 14812)
(Dyeo and dying-Plastics)

- --- - -- -- - --- ---- - --- -- - - - -
FOLYAKOVAi ~ - MMTSOVA, I.B., TATEVOSIYAN, G.O., nauchnyy red.;
C I - ; IM - .0
TISHCH*Ew- . N.I., red.; TRUSOV, N.S., tekbn. red.
(Manufacture of toys from plastics]Proizvodstvo igrushek iz
plasticheakikh mass. Leningrad, Goomestpromizdat, 1962. 318 P.
(MIRA 16s2)
(Plastics) (Toys)

34948
S/19 62/000/003/007/010
S-1 ,p Is- D 0 0 B101X-147
AUTHORS: Tatovostyan, G. 0., Va-gnot-finva- T.D
TITLE: Problem of weather resistant film materials
PERIODICAL: Plastichoskiyq massy,-no. 3, 1962, 44-- 51
TEXT: Films made of polyethylene (PE)i pol,,vinyl chloride (PVC) plastic-
ized with a:BGT (VSF) plasticizer, or PVC type 230 were exposed to
atmospheric influences or to the radiation of are lamps or mercury-ouartz
lamps. Aging was tested by measuring the tensile stren&h d (kj:/c9) and
the relative elonEation F_ at the moment of breakinC. For PE, graphs
d versus T, and F_ versus T, where i . time, were DIfted, and a-in- wa3
assumed to end when FE reached 50Vj' (T50)' Por PVC, aCing was assumed to
end with the occumnee of brittle fraotural when bent 1800 at room tenpe=r-
ture (rDCT 5960-51, COST 5960-5l)- Results: (1) Under atmospheric
influences,aging of PE was MO) faster in Fergana than it was in Mloscow
('r 50 in Moscow 16.0 days). (2) In the laboratory, aging in arc light
yielded comparable results. A conversion factor K - solar radiation
Card 1/3

5/191/62/000/003/007/010
Problem of weather resistant ... B101/B147
houro/laboratory light hours - approximately 3.0 was found. The ratio
Ir Moscow, daya/Tlight hrs ,, 1.737, 'Fergana, days/'vlight hra whs 0*421*
(3) I-To comparable results were obtained with H,-,, lamps which cannot be
used for age tents since the procenses are completely different. (4) A
1.51,19' addition of carbon black to PE increases its light resistance:
without carbon black F- dropped from 400 to 501;~) after 300 hrsl with carbon
black it dropped from 533 to 38%j- (5) Reinforcement of PE with cotton
fabric (percale type A (A)) also increased its service life;
Ir 50 -600 hra. (6) Stabilizer additions to PE showed the followint;: with
2-hydroxy-4-octyl benzophenone: %50 - 252 in Moscow, with phenol -
styrene combination : 7 50 - 338 in Moscow. (7) In PVC stabilized with
lead silicate, brittle fracture occurred after 367 hrs in arc light.
(8) Service life was increased to 954 hrs by lead stearate +3A-5 (ED-5)
epoxy resin owing to synergism. (9) Effect of stabilizers: PVC 230 had
Tloo * 1727-5 hre without stabilizer. Addition of diphenylol propane or
1,1-bis-(4-hydroxy-phenyl)-cyclohexane gave 1 100 , 2162. 2,21-4,4'-tetra-
Card 2/3

S/191/62/000/003/007/010
Problem of weather resiatant ... BIOI/B147
hydroxy sebacephenone (,r 100 ,2350 hro), 2,21-4,41-tatrahydroxy
adipophanone (T 100 "2459 hro), and 2)2-bis-(3-methyl-4-hydroxy-phenyl)
Propane (,rloo - 2715 hra) had the best effects. Z. V. yopova, Ye. N.
hiatveyeva, and A. S. Danyushevskiy prepared the specimens. There are
8 figures, 3 tables, and 5 Soviet referencen.
V4/
Card 3/3

40207
511911621000100910111012
Bi01/B144
AUTHCRSt Antropovat N. Yuzne_ta.ova_,_I__J11__-j_1~t evoolyant G. 0.9
Sharova, A. V.'
TITU: Surface treatment of theM'--4 (PK-4) film with stabilizing
substances
PERIODICAL: Plasticheakiya massy, no. qj 1962, 61 - 64
TEXT. In order -to stabilize the PK-4 polycaproamide film used in
agriculture it was treated with potassium, iodide, manganese chloride,
copper sulfate, potassium bichromate,R -naphthol, benzophenone, resorcinol
dicalicylate, resorcinol dibenzoate, formaling or tannin, The chanees in
the tensile utrength 00 and br akin& elongation & were tested after
artift'ciel aging by ultraviol:t (Hg larips) or Qrc lightf or after.
natural aging under atmospheric conditions in Moscow or Fergana.
Potassium iodide,A -'naphtholl,benzoplionone, potassium bichromate, and
tannin-ahowed a sliCht stabilizing effect against ultraviolot irradiation.
The data -:ot by irradiation with arc lumps were better compdrable with
those obtuined by agine under atmospher-io corditions than the data from
Card 112

S/191/62/OCC/009/011/012
Surface trcatment of the ... MOI/B144
ultraviolpt irradiation. For r, measurud alon6 the nonstabilized film
and alonK the film rtabilizod by tannin the followine data were obtained
respectivel,ys nonirradiatod 371, 452 kC~cc12j aftor 50 hr ir)radiation 395,
677; aftor 120 hr 5C0, 6301 after 140 I,r 316, 36( kg/cM2. The durability
of films exposed to atmospheric effects was 3 months in Noscow and 2 '
months in Fer&ana. Treatment with 1~ taBnir, solution reduded the thermo-
oxidative destruction of the film at 200 C to 1/7 as compared with
untr-jated film. Untreated film contained 11.7% products soluble in watdr,
that treated vith tannin only 3i3~,. Treatment %vith tannin chanees the
optical properties of the PK-4 film. Thu maximum of liGht absorptiont
which i3 250-310 up for.untrouted fIlm, shifto towards 280-400 n*. The
useful life of the filn ie elightly increased by treatment 'with tannin
and this also renders the film more frost-resistant. There are 2
figures ;~,nd 4 tables.
Card 2/2

4*11, 0'.
40906
B/i9IJ62/000/010/001/0io
AUT110IIj i lie DI Kovarokaya, 11. M., Levento I Dral
%j:n, L. v8
Sidarov, V. ":Iah
G, 'V. AxLkaxA+-M-P- A. tk.~, V.
Troi mIn,1G. 6.1 Tatevoslian: 0. 0., Kuznetsova, 1. B.
TITLEs Jt!.billlation of p6lyamide films for agriculture
PFRIODIGALs Plonticbeakiye mosey, nq. 10,,.1962, 6
TLIT, , Prnto.tio. of polyamide films, type 54, an used in hothouses. arid
aLlon; from arrectn.or ph* 6m and tharmo6xIdatIon,'was+teated by trying
varloiia nd-litiven under Y.!i6us test conditions. - The following were added'
its ultrnviolot lipht nbeorborne 2-hydr*XY-4-mothoxy-bonsophonone Oh G~
.(OMBF) (I)9 2-bydro)4-4-alkoxy-bonsophenano (a fbixtur:.of benzophenone:
*ita, vnrin
us nllgoxy froupsIof th.e.type 007 H15 , OC H7 or 0 9 9 ) (it) and
2-hyAroxy'-51-motbyl-bonsotriasole (Tinuvin) (111). As antioxidants, KI
and doppor naphth nato and or4unio stabilizers of the following ty a were
usads .4) derivatives of aromAtic aminesi 2) phenol d*rivativ 35 aromatic
oxamineal 4) 2,6-4itert-butY~-4-mothyl-phonyl-pyrocatoohin ph::Plbito OonO4 :t
Card"1/2
-'7 -7-

S/19i 62/000/010/001/010
6tnbil17.ntlon of ... YB I !
B101 Bie
Polyamido film "alanka producci by condensation, namely heXamothylene n4ipi%.
nate and 4 -caprol.-ictam at 260 C in an N-atmoophora, were subjected to
.thermo- -ind photooxidntive action. Light sources were carbon-aro'qnd
morcury,qu-rtz lampa, typo nFK-2 (PR4-2). Temperature in the test h b
Win 70 It POC. Thormoozidation moaaured by Aho drop In oxygen-pressour7ZO; -Y
eliminated most officlently by the pyrocatechin enters and phanyl-p-naph-
thyl-wainc. It v.lao found that stabilisers 'of the OILBY and Tuvin typee sat' 'l"
an antioxidants. ilh6tooxMation experimen'ta showed the followlaf rosultat ~
in moat cocoa the elonLisi,ion at rupture dropped even on Initial *xpoeure. t
After 200 hru of exposure time, breaki ng tenacity of both stabilized and f
nonattibilized films fall by approximately 20 - 25~. Ageing time until
embrittlument wna determined. Without an inhibitor it began after i" hro
or expocuro to the light of n Optimum resulti were obtained
101 pjrcontechin *#torn W h4r8r3,la71p+ copper naphthen1tj 260 hro).and
wontover) o ((2,6-di-tort-butyl-Wroquiabne)) (240 hre . I Different so-
tion of the light from the are lamps and tbo.maroury lamps;was explained
b apeot m differoncee. Vurther fibld tests *ro reconmi Pn4ed. There are
JYf igure and I tables
ard 2/2

h1918
k-
3/191 62/000/011/014/019
B1 ~ YB1 86
AUTHORS: Tatevoslyan, 0. 0.1 Losevs Is Pop Kusnetsova, I. B.
TITLE: Chemical analysis of polyvinyl chloride plastics subjected
to photoaging
PERIODICAL: Plasticheskiye massy) no. 11, 1962,-59-62
TEXT: Polyvinyl chloride plastics of the t~p so 230, 239, 251, and 489
with a composition of 56-70% polyvinyl chloride, 21-33~ liquid
plasticizer, and about lc~4 stabilizer were irradiated at 700C by carbon
arc lamps (6BO-1000 hre) or mercury vapor lamps (24-180 hrs). The changes
in composition, tensile strength, and resistivity were studied. The
composition was arrived at successive extractions with ether, acetone,
benzene, and chloro benzene, by determining how much plasticizer remained
in the plastic after irradiation, and by determining the chlorine content.
.Results: (1) The loss of plasticizer as referred to the total weight of
plastic was 6-10% after irradiation by arc lamps, and 11-15% after irradia-
tion by*Hg vapor lamps. It is noted that determination of the weight lose
alone leads to deviating data. (2) The chlorine content decreased, but
on irradiating with lfg lamp this was masked by the intense loss of
Card 1/2

S/1 91/62/000/011/014/019
Chemical analysis of polyvinyl ... BIOI/B186
plasticizer. (3) The resistivity of non-irradiated specimens was in the
order of 1012 ohm-cm, that of,specimens irradiated by are lamps in the
order of 10 13 1 and that of specimons irradiated with Hg light was
10 14 ohm-cm.2 (4) The tensile strength of non-irradiated specimens was 2
217-280 kg/cm . Under are lamp irradiation it dropped to 105-176 kg/cm
under H9 light irradiation, it dropped at firstg but then increased to
238-328 kg/cm2- Conclusions: Destruction processes prevail in arc lamp
irradiation, and structuration processes in Hg light irradiation.
Structuration processes increase the tensile strength and the resistivity,
and accelerate the volatilization of the plasticizer since struoturized
PVC is no longer soluble in it. There are 5 tables.
Card 2/2

8/191/63/000/002/013/019
B101/B186
AUTHORS: Tatevoslyanj 0. Ott Kuznetsoval I. B.
TITLE. Long-time and alternating effeato of water and molet air
on plastics
PERIODICALt Plaetioheekiye massyl no. 29 1963P 52-50
TEXT: With,a view to uses of plaotics in building and agriculture the
following materials were tested for changes in physicomechanical and dit~
electric properties due to the effect of water and moisture; prees-mold94
homogeneous thormoplastios suoh a" styrene copolymers CHTT (SNP) p MG (Me)
and MCH (MBR), polystyrene, polypropyliine, polyamide 60, Butvurw ethyl
collulose etroll molded powder-filled inhopiogeneous thermosetting plaotios
based on phenol formaldehyde resins including such modified with rubber,
PVC.j or polyamide reeinj monolithic phenol aldehyde plastics based on
novolac resins with organin curing agentl thermosetting laminated plastici
based on phenol furfural or polyester resins with glass fiber reinforoemen4.6
The toots covered the water adsorption at 20 or 400C and the adsorption of
moisture at 4011C during 1-56 days by weighing the moistened and dried
ard
C
1/2

S/191 63/000/002/013/019
Long-time and alternating.&** H1 01 YBI 86
specimens. The change I n weight after five 24-hr.dippings into 20*c; water
and drying at 40PC.was determined. Conclusions drawn from the tabulated
data: (1) Permanent action of water or moisture produces the greatest
changeo of physi come ohani cal and dielectric properties in thermosetting
plastics, and the least In thermoplastics. The great changes in thermo-
setting plastics are due to capillary formations. (2) Among thermosetting
plastice.the highest water adsorption In reached by materials based on
novolao phenol formaldehyde resinu, the lowest by material6 based on resol'
or novolac and resol resins modified by thermoplastica. (3) 200G water
changes the properties in the same Wal as 400C air moisture, so the simpler
200C water teat is to be preforredi 41,Long-time action of water changes
the properties moro than alternatei.M8 v. ning and drying. (5) The tests
ean be used to estimate the ut1litij 01'~Iaetics under atmospheric influen-
ces and to help in their proper ael-Ation. There are 3 tables.,

S/191/63/000/003/016/022
BlOi/B186
A'.'TIIORSt Kuzneteovat 1. B.9 Tatevoslyant 0. 0.
TITLEs Standard method for testing the weather- and lightproofnose of.
plastics
PERIODICALt Plastichookiye.masay, no. 39 1963t 54-59
TEM In 1963, the POCT not 10226-62 (GOST no. 10226-62) standard
published in Standartizatsiya, no. 3, 1962, was introduced in the USSR to
standardize the testing'.of weatherproofnese.and lightproofneas plastics.
Some explanations and recommendations for applying, this standard are given*
Weatherproofne3a is tented in various climatic regionse
The specimens are ;o,
mounted on frames fixed at an angle of 4500 facing the south. Two of theme
frame constructions are described. Equipment such an heliograph# Tani-
shevokiy pyranometerg ombrometer, thermometer# psychrometerp and anomonster
is recommended for opeciai' meteorological stations in caves where no re-
gular reports are obtainable from a state meteorological station. calibra-
tion of the pyranomoter according to the actinometer data from a State
meteorological station is briefly described. The laboratory conditions, the
Card 1/2

. S/191/63/000/003/016/022
Standard method for testing BIOI/B186
AMTTCT-2-4-2 (AIPST-2-4-2) apparatus is used. It consists of a case mount ad
on a rotating holder, for testing the samples in -horizontal or vertical po-
sition, two carbon-aro lamps, four mercury-vapor lamps# two fens to mainteLa
a temperature of 20-9000t a moistening apparatus# and signaling system
which indicates irregularities or when the rotating cases atop or a lamp
faile, otc. Measurement of the light intensity with the Yanishevskiy
pyranometer is described. There are 3 figures.and 3.tables.
Card 2/2
T':

TATEVOSIYANO 0.0s; KUZN.ETS.OVA#.I.B,; LAMINAq ReAe
Aging of polystyrene under the e"ect of ultraviolet light.
Plast. savvy no.8t66-67 163. (MIRA 16:8)
(Styrene polymers) (Ultraviolet rays)

EpR/EWp(j)/EpF(c)/EwT(m)/BD19 AFFTcA9D P&-4#o-4/Pr-4
L 1 M-63
RMIWWIMAY
ACCESSION NR: AP3006531 S/0191/63/000/009/0010/0012
AUTHORS: Tatevoolvan, G. 0,;ILosev, I. P. (Deceased);
Kuznetsova, 1._Bo
..........
TITLE: The effect of plasticizer upon light aging of vinyl
blend.
SOURCE: Plasticheskiye massy*, no. 9, 1963, 10-12.
TOPIC TAGS: polyvinylchloride, vinyl blend, light aging,
plastics, plasticizer.
ABSTRACT: Authors showed that the.aging process of a
plasticizer does not increase its specific gravity, but
increases its acidity, which indicates a decrease of the
specific volume of electrical resistance. The resistance
of polyvinylchloride plasticizer to the effects of light
energy is primaril determined b aging which takes place
in the polyvinylchloride resin .PrAs a result of this aging,
the mutual soLuDi=y in the Fesin and plasticizer changes.
Card 1. / 2

L
ACCESSION NR: AP3006531
the observed continuous change of plasticizer quantity in
the afing process ofovinKl blend by light'did, not show
:a dec sive effect up n t e stability. Orig. art. has:
3 tables.
ASSOCIATION: none.
SUBMITTED: 00 DATE ACQ: 30Sep63 ENCL: 00
SUB CODE: CH NO REP SOV: 002 OTHER: 0011
Card 22

ACCESSION NR: AP4046022 B/0191/64/000/009/0032/0037
AUTHOR: Kuznetsova, 1. B., Tatevoslyan, G. 0.
TITIX- - Change In the properties of polyamide film under the influence of light
SOURCE: Plasticheskiyo mtwsy*l no, 0, 1904l 32-37
TOPIC TAGS: polyamide, lighti aging, spectroscopy, tensile strength, elongation, light
absorption, polyamide film, film PK-4
ABSTRACT: The changes In the properties of polyamide film PK-4 during aging under fa,
atmospheric and laboratory conditions were studied by spectroscopy under the separate
or combined Influence of artificial changes In climate. A colorless un6tabilized PK-4
film was used as the test sample, with an elongation at break Eo = 292% and maximum
M2
tensile strength & 0 = 388 kgs/c The test sample was subjected to atmospheric aging
on a laboratory apparatus, to atmospheric aging in suspension, excluding direct solar
radiation, to artificial aging at 70C under artificial light (500W incandescent lamp, arc
and mercury lamps), and finally to aging under the Influence of moisture.with are and
mercury ramps. The following characteristics were determined: yellowing factor, %
mwdmum tensile strength (e.); relative elongation at break %) for 80-mm-long and'.
1/3
Card

ACCESSION NR: "4045022
8-mm-wide strips; the monomer content, by extraction with boiling water for 15 hours;
the molecular weight, from the viscosity of a 0. 1% solution In 40% F12SO at room tem-
perature; and the ultraviolet and infrared absorption spectra. The experimental data are
plotted. -t and d -t curves show that variations in relative humidity and atmospheric
drying greatly affect the properties. The process of thermal aging proceeds relatively
slowly, however. At a temperature of 45-48C in visible light, the change in properties
can be attributed to light aging. Yellowing of the film appeared after 145 and 75 hours
of irradiation at intensities of 0. 442 and 0. 866 Cal/CM2 min., respectively. The mol.
weight dropped from 23, 600 to 19330-19062. Visible light together with atmospheric
oxygen affect the polyamide film markedly causing Its destruction. In samples kept In
distille water until the weight changed, ~,increased to 365%, and cf decreased to 267
kgs/cm. ; in dried samples the opposite occurred. In addition to moistum, the monomer
content also affects Lhe film properties. The effect of heat under light from incandescent
and mercury-quartz lamps was also studied. The combined effect of heat, moisture and
light was investigated, and analytical data for monomer content and oxygen content are
'tabulated. The absorption of light by the film before and after aging under differentcon.;,
ditions was investigated and the changes in light transmission In the ultraviolet and in-
frared regions of the spectrum during aging are discussed in dotaiL Under the influence
2/3
Card

ACCESBION NRj AP4045022
of hout and visible light, the absorption in the region 250-290 mp Increased rapidly; later
it Increased Ions rapidly In the range 290-680 mil. During aging under atmospheric con-
ditions, the general light absorption decreased in all regions of the spectrum. it is im-
portant that the light absorption Is smaller after aging In all cases, especially marked
changes being found In the regions 800-000, 1800-2800, and 3600-4000 cm-1. Orls. aft,
has: 6 figures and 2 tables.
-ASSOCIATIONt None
SUBMITTED: 00 ENCL: 00 BUB CODE: MTO'P
'NO REF SOV: 021 OTHER: 016
Card 3/3

- , ~i7 1 -. I . . -. I. , - I
.. , ., e , .;-I- . I .I . . 1.

I .-- I - I--
f I
7L,
KH. L.S.. kandined.nauk; KUZUSTSOVA I.D., kend.med.uauk;
MALINOVSKiYA, T.N.
Controlled bronchograpby with sufoiodol [with summary in Anglish].
Yestooto-rins 19 no.3slOO-103 My-Ja 157. (MIRA 10tlO)
1. Is kafedry rentgenologii (zav. - prof. Yu.N.Sckolov) TSentrall-
nogo institute usovershoustvoveniya vrachey.
(BRONCHI, radiography
contrast sodium, todized poppy seed oil)
(CONTUW KSDIA
iodired poppy seed oil in bronchography)

JK ZNETSQY~A, FALKINA., D.A.; ANONHINA, K.P.p red.; KREMENETSKATA,
K-7.-,red.; ELIBERT, O.A., red.
[Scientific and technological information in the U.S.S.R.
and abroad; a bibliographic Index to the literature
published in 1960 and 1961) Nauchno-tekhnicheakaia Informa-
telis, za 1960-1961 gg. Moskva, 1962. 215 p. (MIRA 16t10)
1. Moscow. Vasooyuznyy institut, naucbnoy I tekhnichaskoy in-
formstail.
(Bibliography-Soience) (Bibliography--Technology)

Thiodiphouylastize is uot toxic to fishes of the Volga delta. Medparas.i
paras.bol. no.6-.563 I-D 133- (mu 6ti.2)
1. ;X,r&vpIyekogo'.UG5qynOTOgo filial& vassoyUsnogo nauchno-Issledovatell-
skogo Instituta morskogo rybnogo khozyaystva i okeanografii.
(ThiodiphenylamiW) (Volga-71shes) (Fishes-Volga)

KUZMSOVA-i-I-.-I-.-"KHLATIJ91,-Y6-.-S.,-x~e-d,--, GOTLIB~_R.A, -taktuired,
~reefnn pike parch on spawning and rearing farms In the
Volga Delta] Razvedenia sudsks. v nerestovo-vyraotnykh
khosiaistvakh dellty Volgi. Moskva, Pishabspromizdat. 1955.
16 p. (MIRA 12s3)
(Volga Delta--Perch)

KUZNZTSOVAj I*Isi kandobiologichookikh nauk.
Ilaments of gas exchange in young bream on fish spawning and
rearing farms of the Volga Delta. Tru,dr VNIRO 32:76-91 '56#
(MIRA 10:10)
(Volga Delta--Dream)
(Respiration)

KUZIMSOVA, I.I., kand;blol.nauk
114mente of gas exchange during early developmental stages of bream.
wild carp and pike parch. Trudy sov.Ikht.koz.no.8:346-358 1 58.
(MMA Ilt2l)
1. Tasplyskiy filial Vaesoyusnogo nauchno-tooledovatellskogo Inatituta
morskogo rybnoro khosyerstva i okeahografii.
Wspiration) (Corp) (Perob)i

26-58-6-30/56
AUTHOR: Kuznetsova, I.I., Candidate of Biological Sciences
TITLF. A "Chomicnl Theory" of Fish,Migration ("Khimicheakaya teoriyall
migratsii ryb)
10
PERIODICALi Priroda, 1958, Nr 6, p 102-104 (USSR)
AB5TRACT: The author reports on the spawning habits of two Volga fish
varieties: the sazan (carp) and the vobla (roach). They in-
variably choose recently inundated plots for spawning, but
avoid places that have been covered by water over longer
periods, to protect the spawn from enemies and to furnish the
young fish with sufficient food. Hydrochemical observations
have proved that the chemical composition of inundated plot
water standing longer than five days, differs considerably
from water of recent inundation, which shows an important in-
crease especially of chlorine in the first few days of inun-
dation. Hence it must be assumed that the above-mentioned
fish are being guided by a "chemical scent".
Card 112 There is 1 diagram, 1 table and 1 Soviet reference.

A "Chemical Theory" of Fish Migration 26-58-6-30/56
ASSOCIATION: Kaspiyakiy nauchno-iseledovatellskiy institut rybnogo
khozyaystva i okeanografti (Astrakhan')
(Caspian Scientific Research Institute of Fishery and Oceano-
graphy - Astrakhan')
Card 212 1. Fishes-Higration-Chemical theory

KU7?4V,,TSOVA, E.I.
Survival increase in the progeny of carp (Cyprinus carpio L.).
Zooi. zhur. 41 no-91l367-1373 S 162. (MIRA 15ill)
1. Volgograd Branch of the State Research Institute of Lake and
1
R
iver nahery Management.
(Fish culture)

KUZNETSOVA I.L.
Increasing the productivity of fisoands by regulating the vater
regime and timing the reproduction of fishes. Vop. ekol. 5:112
062. (KERA l6s6)
1 Volgogradskogo otdeleniye Gosudarstvennogo nau#no-issledovatel,17
siogo instituta ozernogo i rechnogo rybnogo khozyaystva.
(Tsinlyansk Reservoir region-Fish culture)

ACC WRs
AP7002603 S OURCE CODE; UH/0413/0AW/023/01-10/0110
MENTORS: Agayovp As Iq Kollchenko, A. V.1 Malkin, B. D.j 0~6 Iti-
Kumptos
Nikitin, G, M,; Gusman,, M. T.
ORG: none
TITLE:' A stopped rolling axle support. Class 47.. No. 189251+
SOURCE: Izobrateniya, prowlshlenrqye obraztsy, tovarWo znaki, no. 23, 1966, no
TOPIC TAGS: antifriation bearing, ball bearing, bearing race - I
ABSTRACT: This Author Certificate presents a stopped roning axle support containing
thrust roller bearings, spacing collars, and an annular elastic element (3ao Fig. 1).
To eliminate loose We holes and to increase the efficiency 'under cbmamic loads,
the ball bearings of the support are placed in two rows.. with the balls running be-
tween the outside flanges and the-internal flange. The annular elastic element is
mounted on each side of each ball bearing at a sma3.1 distance from a spacing ring.
A split bushing is placed between the inner flanges of,the corresponding ball bear-
ings,
Card 1/2 was 621.822.3

ACC NRs AP7002603
Fig. 1. 1 - bans; 2 outside flange;,
3 - inner flange; I+ - a=ular,
elastic slomentl 5 - space;
6 - spao~ing ring; 7-.split
bushing
Orige art, has: I figurs'.
SUB CODE: 131 SUBM DAM 03YAr66
2 /2

NIKITINA,, To.I.; BERZINA., A.Pq Y.U*TS0VAr I.K.; SOTNIKOVv V.I.
- I
Svonbergite in the Oornyy Altai. Dokl. AN SSSR 149 no.4t942-9"
Ap 163. 1 OURA 1613)
1. Institut goologii i geofisiki Sibirskogo otdoleniya Af', SSM.
Pnidotavlano akademikom V,S.Sobolavym. .
-(Altai Mountains--Svanbergite)

AUTHORs Sheynker, Tu.ffo, Xuznetsova, IX 76-i24V27
-------------------
TITLEt On the Tautomerism of Some Derivates of Heterocyclic Compounds
(0 tautomerii nekotorykh proizvodriykh geterotaikliaheskikh
9oyedinaniy). V. Spectra aa Structure of Some SulfW'Jand as
M Spektry I stroyeniye nekotorykh sullfanilamidov)
PERIODICAL Zhurn&2 Pizioheskoy Xhimils 1957# Vol. 31, sir 129 pp.2656-2662 (USSR)
ABSTRAOTt Reference in made to the preoeaing paper [Ref - 17 , and -oy means of
infrared, and , in Individual oases, also of ultraviolet spaotra, the
ntzuoture of 2-sulfanylamiaa3 of pyriaine and of pyrimidine, as well
as of some suirwismiaes of the alicordlio series (which are used as
medical preparations) is investisatea. The measuring method ban al-
ready been described in previous works. From the data obtained it
follows that in the pyridine and pyrimidine series, which have
2-Oulf lamidets in the crystalline state, have an imido structure
(1), (171, and are derivatives of 2-pyridomine and 2-pyrimidonins.
As in cases investigmted previouslyt this is due to the strong acid-
ifying influenoe exercised by the So 2 group on the wMe group NH,
Consequently, the ratio of the basic proportion of the nitrogen
atom outside the ring, and that of the nitrogen atom within the ring,
Card 1/3 changes in favor of the latter. It Is shown that in the aqueous

On the Tautomerism of Some Derivates of Heterocyclic
Gompounda. V. Spectra and Structure of Some Sulfanylamides
Oard 213
76-12-807
olutions the 2-sulfanylamiaopyridin shoym essentially an Wdo
ruoturep whereas in alcohol solutionso besides the imido-foms
N
also the amido-form is contained in substantial quantities. The lat-
ter form prevails in diczan solutions and the content of the amido-
form can be evaluated by 99%. In the case of the sulfanylamides of
the pyridin, a tautomerio system is concerned, which is very close
to the state of equilibrium. Further it is shovm that -the sulfanyl-
amides of the alicyolto series (sulfarUliacetamid, sulfanylurea
~(urosulfan)), both in crystalline state, as well as in solutions,
have an amido-struature. The lAtter because they keer the same strip-
systems in infrsrad spectra of such Bolutiony (alcohol, dioxan)p
and especially the cakhonyl-atrips (1700 =7') under the conditions
prevailing here. Gonsequentlyl the aoid-propertioa of the NH-group,
in spite of the strong acidifying effect of the sulfanil-group do
not increase to such an extent that the amid forms (V) and (VI) be-
coem more acidifercue than the ImIdo-forms (VII) and (VIII). The
obtained data correspond to the oonoeptione of the acid-basio ohar--
aater of the amiao-imido tautomeric equilibrium. It is finally shown

On the Tautomerism of Some Derivates of Heterocyclic 76-12-8/27
Compoundso V. Spectra and Structure of Some Sulfanylmided
that the baoteriostatic activity of the sulfanylandd-preparations
cannot be correlated with the imiao-struoture of their molecules.
There are 5 figures, ana 8 references, 3 of which a" Slavic.
ASSOOIATION: An-Union Scientific Chemical-Pharmaceutical Research
Institute imeni S. OrdzhouiKidalej 908cov (Vaespyuznyy nauchao-
issleaovatellskiy Khimiko-farmatsevtichaskiy institut im.
S. Ordzhonikidze, Moskva).
STBMITTED: Ju3-Y 21, 1956
AVAILABLEs Library of Oongress
Cara V3

B/i)62/61/000/008/005/010
B117/B2O6
T 1700
AUTHORS., Andrianov, X. A., and Xuznetsovag 1. K#
TITLE: The reactions of'ohloromethyl mothylalkoxy~ilanes with
sodium salts of diethyl phosphoric and dimethyl phosphinio
acide
PERIODICAL: Akademiya nauk SSSR. Izvestiya. Otdeloniye khimichookikh
nauk, no. 8, 1961, 1454-1456
TEXT: The authorB,investigated the substitution of chlorine in a-chlor-o-
methyl-alkoxy-silanes by dialkyl phosphorio- and phoij~inio aciA roe to
The sodium salt of diethyl phosphate was prepared according to the method
described in Ref. 3 (Canad. J. Chem 1819 (1956)) and carefully dried
in a vacuum exeiccator-over phosphorus pentoxide. The sodium salt of
phosphinic acid was produced in the usual way by neutralization of,
dimethyl phosphinic-acid in absolute alcohol, dried in a d5rying chamber
for several hours at 1200 t01300C and stored in the vacuum exeiccator over I
P 0 The experimento were mado*in a three-neoked flask with mixer and
2 5*
'Card 1/4

3/06y~ 61~000/008/005/016'
Theftreactions of ahloromethyl.00 B117 B20
sealing, recooler with calcium chloride tube'and thermometer. The experi-
ments showed that chlorine in a-ohloromethyl alkoxysilanes easily reacts
with the sodium salts mentioned. Organic compounds containing Si and P
with an Si-C-0-P bond are formed thereby, containing simultaneously
functional groupe at the silicon atom. 'The synthesis of the compounds
mentioned was made according to I I
_N set
1) (CH,),-SI(OR),_,+NnO-P-.~.(CH9)t--(CH.s).-Sl-(OR),-,;
Lip 0 H,'
~"P-Pflh
0
and :2) (Cffs),-SI (OR)&-,, + NaO-P-(OCjHs)s (CHJ~-SI-(OR)j_,
I~Hj
_P-(OCjH&)s
0 1 - .
0
shoved.tha~,t%e
where R-C 2H5; lie(CH 3)2 nm;1.2. The yield of the products
Card 2/4 CH2Cl

64
I / 0)"6'
E
P?!1/000/008/005/010
B
TITe reactions-of chloromethyl... B117 B20.
salt of di6ethyl pho'sphinic acid reacts more easily. new organic compoundi
containing Si and P were obtained as results of the reactions carried-ouW;
methyldiethoxyoilyl mathylester of dimethyl phoaphinio acid (I)i dimiFthyl'.
ethoxynilyl methylester of dimethyl phoophinio acid (11); methyldiethUy-
silyl methylester of diethyl phosphinic dimethyl ethdxyeilyl
methylester of diethyl phosphoric acid (IV); t stramethylsiloxy-l,~- .4i
disilyl methylester of dimethyl phospbinio acid (V). The propertids of --
these compounds are comprised in the Table. There are 1 table and
3 non-Soviet references.-- The three referenoes to English-language
publications-read as folloWs: A. Canavan, C. Eatorn, J. Chem. Soo.' 195~,
375); W. Garden, N. Thompson, Angl. pat. 815231; 24, 06, 1959; R. McIvor,
C. McCarthy, C. Grant, Canad. J. Chem. a, 1819 (1959)-
ASSOCIATION: Institut elementoorganicheakikh soyedineniy Akademii nauk
SSSR (Institute of E~emental-organio Compoundat AS USSR)-
SUBMITTED: October 12, 1960
Card 3/4

2t272 5/o62
a, etsOve 1. it", sthy' X
U ~U%n hinto Set
ar DOI
is tria"Ityl(srtle'r-'e"'Of dimethl hi,jobesy-i~Lh
Reaction 0 Sethi I es tae-jenile
-IT LJ~ etho%Y still J.Z.Vestila. roup by
. 555?~. 1192 - 1194 the allco%y 9
UV no-
XV I r1ous orga
.O&emils na I j961i tion 0 Va oily'
10 sub6t it %X UPS on etho%y 0 at
naux I no ell th e end gro aimethyl silan
t So the ting &-r0%1 trietbil
inIeStigs hes, thil " OC an& r%edX
thors dAG5 +hot by j+ rie f0
frh e a U old Ta h t 150
hinjo a foun& old V t W)o - - act ter Of
TF,)LT I phosy t % So hinjo a te6 5 hosphinle Uet e
Pounds - SP separs thy' V i.111- git
aimetlay 0 -nil gas , jime e Or e
m Of dijAct - Pho 0 e hO%y a sil
alcohol t &r0% an isi,10%
a ester -1 ester dimethy iuLet at
~jl 1
'19 thy, m,thj I Of lie I -
methy of it ne et tol + e 1-3 61 e 0
ph
stio From the reS hll P I eth g ere 0
a r disilo%a d with diSe A~M I
aiSetbil -6imet 'Pe
and res
5- 14. 'aic Be i,snet. acid id,
in 64 Y 'hoslDhl- i n',c
Phi
Set'hyl P . . hydro%Y phosphin 0 hos
di 11 diphenY dimethyl j climethy, V
Seth'. , ester Of ester 0
Sethloxane jethl'-
aist
CaT& i/A
28272 s/062/61/ooo/010/007/08
B117/B101
Reaction of trialkyl ... atom.
are substituted on the silicon
Not only one but two ethoxy groups hyl di-
Thus, from the reaction of dimethyl phenyl hydroxy silane with met
ethoxy silyl methyl ester of dimethyl phosphinic acid at a ratio of 209
1,5-dimethyl phenyl-5-mothyl trisiloxane methyl ester of dimethyl
phosphinic acid was obtained. similar reactions were conducted with tri-
I ihenyl hydroxy silanea" All reactions were con-
ethyl. and dimethyl dip silane and methyl
ducted without a catalyst. The dimethyl phenyl hydroxy
diphenyl hydroxy silane used were produced by the method of
Y- A. kndrianov and N. Delazari (Ref. 3: Dokl. AN SSSR 1229 39 393 (1958)),
and dimethyl ethoxy silyl methyl ester and methyl dietl~O-X-y silyl methyl
ester of dimethyl phospbinic acid by the authors, method described in
Ref. 4 (Izv. AN SSSR, otd. khim. n. 1961, 1454). Ethyl alcohol produced
during the reaction was distilled off and identified on the basis Of
boiling temperature and refractive index. Reactions conducted yielded
compounds not yet described with 2 or 3 silicon atoms containing a di-
methyl phosphinic group. The compounds obtained are colorless liquids
readily soluble in organic solvents and may be distilled in vacuum. Their
properties are listed in the table. There are 1 table and 4 referencesi
2 Soviet and 2 non-Boviet~,
Card 2/4

20272 S/062/61/000/610/007/018
Reaction of trialkyl... B117/B101
ASSOCIATIONs Inatitut elementoorganichookikh soyedineniy kkademii nauk
BSSR (Institute of Memental organic Compounds of the
Academy of Sciences USSR)
SUBMITTEDi April 6, 1961
Legend to the Tables (1) number; structural formula; (3) boiling
point, OC (p mm, Hg)1 (4) foundl (5N)aleulated.
3/4

28670 J1-
0/020/61/140/002/015/023
A B103/B101
AUTHORS., Andrianovj Ko A., Corresponding Member AS USSR, kuresheval
No As, Kuzneteoval 1. K,t and Garkhardtp B. 1.
TlftEi Synthesis of polymers of regular structure of the polydimothyl-
Biloxane series
PERIODICAL: Akademiya ftauk SSSR. Doklady, v. 140l no. 2', 1961 365-367.
TEXT: The polycondensation of the mothyl-diethoxy silyl-methyl sot
or 0t
dimethyl phosphinio &aid (1) with various alo-dihydroxy-dimethyl'eiloxan'es
II) was studied. The' distance between the dimethyl phosphifie groups,.
NIP) could be varied by using II with different numbers of dimethyl-
siloxane links between the OH groups - The DMP groups were evenly,
distributed along the molecule chain. II was synthesized by the reaction
applied for diphenyl ailanediol (Ref - 3 1 see below). Its data are
presented in Table 1. IX react with I at 1700C without a catalyst in the.
following wayi

2867o
9/020/61/140/002/015/023
Synthesis of polymers of regul,ar B103/B101
Hj)j CH
tit + M HO_ 1,0 H-
P(CHO)l
-0- 0, - jCH-,
&6) + 2W,4H&OH.
O-P(C%)$
The end point:of the reaction was determined from the quantity of liberated
ethanol. It wag 76.50 of the theoretical amount at a degree of polymeriza-.
tion n a 9, and 73% at n a 13- At n a 53t the reaction was considered to
be completed when a conatent viscosity was attained. The molecular
weights of the polymers 'obtained j determined by the visooeimetrie method,
were 2190, 7250, and 31p620. The vitrification temperatures of all these
polymers was low: -110001 -13000. A slight increase of the vitrification
Card 2/4

28670
0/020161/140/002/015/023
Synthesis of polymors of regular ... B103/B101
temperature was obtained by reduaing the distanos between the DMP groups,
The low vitrifiottion tomperstures of polymers with polar DMP groups in
their chains are explained by. the fact that the DUP groups which are
large as oompared with the CH 3t groups, reduoe the paoking density of the
molecule chain. There are I able and 3 references: 2 Soviet and i non-
Soviet. The reference to English-language publication reads as followes
Ref. 33 Yoshio Takiguchug Bull, Chem. Soc. Japanq 12l no'. 6, 665 (1959)-
ASSOCIATION: Inetitut slementoorganiohookikh soyedinaniy Akademii nauk
SSSR (institute of Elemental Organic Oompounds of the
,Academy of Soisnoes USSR)
SUBMITTED: May 171 1961
Card,3/4

3551,32 .coo/003/009 /W4
S/o62/b
Blil/B144
tsove.
and j~,jzrie ethyl methyl' oric-
ohlorom dithi-opho a ph
~.nari ov 1 i~ - I-
an in CL- aibuty
0, chlorine thyl-~
A:UT11QRS oil i e of ate OjdB
'heny
Slabst'tuti du a into a
silarkes by res O-phosph himi
-jTL'F dithi Otdelen'ye
nd silepes
diPhe uX SSsTL ' -17,yestiya' thylet -holLy
- na 19629 456-461)
txaaemlyo 31 oromethyl-me hosph"'Ic
Ohl 1-dithio'p with
na'a'K, DO - Drine in CL- d d,phony ..O.Y811sne -050C
f chli oric. all 6 hre at j30-
Lou 0 h metIly .1dimethyle 10 tholcy
A
substitut! ai thi 0 Pbc,8-Phj Oro 'd f or almetbIle 1,
f2he dialy-'Yl- of horic; horic
beating to 94 0'and
ithiophosp aithiophosp comp
residues 0 il'i re -
by tadied- its yield of.
'08's 8 letbyl-d f aetbYl tions jo
44 n
f to increase I
acids salt 0 yi eld, 0 f diethy 86 es, Ophosph,1%11
9 possible 'a'nte 0
Bsiut , (1i t
a 116 30 of
DO ' .2 Onl"Y -it via 3. yie
. rodUceu tic aT,10 . dipheul t yl-
P stop (1) - tO6lJ '6 j th r O~ an c lorom
1 0 daing 00- 6. W s' h( i & CL -
methy similal thlophool) A
fter 3-4 hre by ain a di an e
Ob tained f dibutY methyletbO74
(-j-1) was salts - 0
P.tass"111 ChIOTOM
acids Ifith
Igloo
Card 1/3
s/062/62/000/003/009/014
B117/B144
Substitution of chlorine jyj aniline also produced
y silane in the presence of dietl jilyl- and methyl-
methyidiethox tstive yields (90 ~) of dimethylethox.YE" (,,I), (IV), (V) and
almost quanti ters of the corresponding acid hyl-dithio-
IiethoxYailYlmethyl es -1,3-di,ilylmethyl eater of diet a 65 ~Y
1). Tetraji )horic acid (Vill) (Yiel
(V iethylsilOxl dithiophoor d from
phosphoric acid (VII)p of dibutyl- lid (IX) (yield 85 ~) were obtaine
and of diphenyl-dithiophosphinic ac ramethyl disiloxane in the presence
romethyltet of diethYl
reactions with 1$3-bie-ablO The catalytic ef*fect
diethyl aniline amounts. cipating in the formation of a
of catalytic robably connected with its parti thoxy silanes. Owing to
aniline is P omplex 'with a-chloroulathyl-methyle of chlorine in
transition 0 f the 0 - Cl bond, this favors the mobility obtained are listed
ionization 0 The properties Of the products
the chloromethyl grOuP*j table and I Soviet reference.
in a .table.. There are elementoorganiohookikh soyedinoniy kkadomii nauk
Institut pounde of th4
ASSOCIATION: 'o of Ejement&j o~ganio com
t,tut
B53B ('no es USSR)
Academy of Scieno
SUBMITTED:' October 169 1961
Card.2/3

Substitution of chlo
rine in... 5/062/62/
B117,/B144 OCC/ 003/ 009/014
rA
Legend to

0o
yna
T. omn. IG
n
20 1
20
d
"An POOP& IfUl
-the Table: p (P. X4 v?. er.) D &
c0 N
(1) Number of
(Clio)% (CIII&O) Sl - Cllspp (oc,116)l
t26 (1)
1,4863
1,0715
81'1
81,M.
the compound; It Clio (ClIlho).891CIIISP (S) (OCIlls)l 150-160 (6) 1,48M 1,0919 80.76 86,75
~2~ Formula; III (CIj2)j(C2II&0) - SjCII*SP(S)(0C4IIrn)j tffi-M (2-3) 1,4821 1.0267 99,82 90,81
3 Boiling IV Clio(Csit&O)DSICI12sp(S)(OCIII*-n)2 M-M (2) t,4770 0,0514 S04,9 105,3
point OC V (C I I')'(C'II'0) Siclis - S - P(S)(Co II0$ UO-220

(P MM HO
(4)
0
'"
6 1, 6056 1,148 1 110, 1 100,4
;
V I CIIS(WIo0)jS1CIfxSP(SXC1H01 -
235
-
Molecular (I-IGP) I,W,8 1, 1545 115,1 114,82
vil
refraction; (5) (Clio), - S1 - 0 St - (Clio),
found; (6) (t-io-) 1,4915 I,tl34 138,4 139,2
calculated;
*) T
t A .H,O)P(S)- IS ~-P(Spc'llo)s
empera
ures Vill (CI`I')'_SI_0-SI(CHx)j
of the bath.
200-204
1,4906
1,0753
176,1
176,42
2(n-C4HoO) P(S) P(S)(0C4IIo-n)j
Ix (CH,)g - 31-0- Sl-(CHs)s
I I I
& T. wt. 126-127
Card 3/3, 1 S P(s)(Colls)II
(C-!I6iS(S)PS

AMRIANOVS K.A.1 DABAGOVA, A.K.; KUZNF,7SOVA, I.K.
Synthesis of unsaturated phosphorooganosilicon compounds of the
ailoxane series* Isv*AN SSSR,Otd,khJ-*n&Uk no.q:jlk4m#666 S 162.
T (MIM 15tlO)
lo Institut 4esentoorganichookikh soyedineniy AN SSSR.
(Silicox~organie compounds) (Phosphorus organic compounds)

5/062/63/000/003/008/018
BIOI/B186
Andrianov, K. A., ~uznetsova, K. and Pakhomova, I.
Reaction of mothyl-ethozy-silyl-mothyl caters of dialkyl-
dithio-phoophoric acids with triethyl-hydroxy-silane
PERIODIOALI Akademiya nauk S33H, Izvestiya. Otdeleniye khimiohaskikh
naukp noe 3, 11963, 500 - 502
TEXT; The authors studied the reaction
(CH3)2'1 i0c2H 5+ (C 2H5 3SiOH (CH 3)2S1'_O_3'(G2H5 3 + C2 H5OHO
CH CH
, 2 2
B-P-(OR)2
pV(OR)2
S
In the case of R - 0 2H5 after heating at 140 - 150 0C the dimethyl.
ethoxy-silyl-methyl eater of the diethyl-dj8hio-phosphorio 0 acid was ob- 1
tained, yield 50 16, b.p. 153OC/2 mm Hg, n5 a 1,46iS, d2 m 1.029. Witi
4
Card 1/2

3/062/63/000/003/006/018
Roaction of mothyl-othoxy- B!01/B)86
R - C H the correspd~ding eotor of 04o dibutyl-dithio-phosphoric acid
4 9 20
was obtain ed.in 40 ~, yield., b.P. 150OC/1-10 mm H9, n. .1-4769,
20
d 0,9947. The struoture of these compounds was identified by their
4
synthaois from 1-triethyl-3-chloro-motliyl-dimat,liyl-diailoxane and
-DotaGaium diethyl-dithio-phosphate.
ASSOCIATIONs Institut elemenioorganichoskikh ooyndineniy Akademii nauk
333R (Institute of Elemental Organic Compounds of the
Academy ot Sciences USSR)
SUB'HITTED: IMay 29 1962
Card 2/2

MASTRYUKOVA, T.A.j 811111M, Yu.N.; XVZI&T
~4~VA I.K.; MiESUNI, Ye.M,;
SAIGWOVA, T.B.; UBACHNIK, ff.I.
Hammett equation in the theory of tautomeric equilibritun. Part
2: Tautomerism, ofa -aryloulfaminopyridines,?otentA21MW
*,atudy,
AO 163.
~qrzt*kbla. 33 no.lQj3328-3335 0 . i
Hamm tt equation in the theory of tautomeric equilibrium.
Part 2: Tautomerism. ofOL -aft;oulfaminopyridines. Spectro-
photometric study. 3336-3342 WMA 16:11)
1. Inatitut elementoorganicheak-ilh soyedineniy All SSSR i In-
stitut khimii prirodnykh aoyedineniy AN SSSR.

ACCESSION NR: AP4025009 0/0062/64/000/00310454/0457
AUTHOR: Andrianov, K. A.;_"s Wwa.1s. K.; Yermakova, M. N.
TITLE: Polydimethylailoxanes containing tris(trimethylsiloxy) and dimethyl-
phosphinoxy terminal groups
7
SOURCE: AN SSSR. Izv. Seriya khimicheskaya.- no.- 3, 1964, 454-45
TOPIC TAGS: liquid polydimethyls:Uoxane, terminal polkiner group, tris(tri-
methylsiloxy) group, dimethylphosphinojq~ group, viscous flow ictivation energy,
polymer viscosity, polydimethylailoxane viscosity, condensation synthesis,
polymer synthesis, -polymer molecule number
ABSTRACT: Now liquid poVdimethylailoxanes containing the above terminal
groups were synthesized by condensation of ot, (4-dihydroxydimethylailoxanes
with the dimethylethoxymilybuethyl eater of dimethylphosphinic acid or trio (tri-
methylsiloxy) ethoxyxilane, and some of their properties (molecular weight,
glass-forming temperature, activation energy) studied. Tho reaction formula to
Card 1/3

ACCESSION NR: AP4025009
presented and properties tabulated. In the end products, n, denoting the numbers
of polymer molecules, was equal to 9, 13, 42, 45, 75 and 120. Viscosity In the
20-120C range was higher in polymers with terminal tris (trimethylolloxy)
groups than in those with the dimethylphosphinoxy group for the same degree of
polymerization. The logarithm of viscosity, inversely dependent upon tempera- I
ture, to also figured. The activation energy of viscous flow, calculated accord-
ing to experimental data in the range studied, decreased upon increasing the
distance between the terminal groups, which may point towards a comparatively
great influence of these groups, as against that of the dime thyls iloxane groupsi
of the backbone. The synthesis to described. Orig. art. has: 2 formulas, 2
tables and 4 figures.
ASSOCIATION: Institut elementoorganicheskikh soedinennty AkadeM.U nauk SSSR
(Institute of Orpnoejawfta Campowdsp AcaderAy of Sciences, SSSR)
SUBMITTED: J00602 DATE ACQ: 17Apr64 ENCL: 01
SUB CODE: CH NO REF SOV: 005 C)THER: 001
catj 2/ 3
V!

ACCESSION NRIA?4025009 malms 101
oil arduml pral MHSOH +
f ol 1. -.1. till
0 1 ('C' H
+(CH
'Jai
jug
(CHS)l P ~-p 041
whore n 45. 73, 1
20
fe'lls
CH
l(Cags woll al 0 JAI I'ositow(CU4104MR&OU
Card 3/3 where n,~

.ACCESSION NR* AP4033366 0/0062/64/000/004/0651/0636
AUTHO11 Andrianovp Ko A91 Kusnatsovaq Is Ke
';TITLEs Synthesis of certain phosphorus-cont&LnLng orS¬Lt&nLu1W
'compounds
!SOURCE: AN SSSR, Izvootiyes SerLya khLmichaskaya, no. 4, 1964,
651-656
iTOPIC TACSt polymersp heat-reiistant polymers# organotLtauLus poly-
imers. phosphorus containing organotitanLum polymers# dimethyl-
-O-T backbone,
phovphLnatolbutrarxytLtanLumg polymers with TL
ipolymer'wLth TL-O-P backbone
:ABSTRACTs Polymers with TI-0-Ti backbones and pendant dLmethyl-
:phosphonate groups and polymers with TL-O-P backbones with pendant
~alkoxy and methyl groups havt been synthesized for the first times
;Honomers with TL-O-P backbones and functional groups linked with the
itLtanLum aton-dLuothylphoophLnatobutoxytLteaLums-of the type
card 1/4

AMSSION NR9 AP4033386
I (CH3)2P-O-jSI - Ti-(wOCIHg),,-,, where nw2, 3, or 4. were synthesized
0
by condensation at 140-150C of dimethylphosphinic acid with tatra-
~butoxytLtanium,, taken in the ratios 2slq 3slg 4sle Hydrolysis of
lbie(dimethylphosphinato) disbutoxy-tLtanium yielded a powdorlLko
'polymer
(CIIS)s P - 01 - TIO
'(polymer 1) which is insoluble in water and the usual organic solvents'
.and has a melting point of 435-460C (thermomachaaLcal curves I and 2
In Fig* 1 of the enclosure)* Reactions of bis(dinothylphosphinato)
,dibutoxytitanium with triethyl- or nothyldtphanylailanolp or of bis
.(triethylailoxy)dibutoxytitanium with dimethylphosphLaLe acid yielded
solid products with a melting point (thermomechanLeal curves 3 and 4
An Fig& 1) and other properties similar to those of polymer to Retero-
.functional condensation of tatrabutoxytitanium with methylphosphisLa g
Card 2/4

ACCESSION NRs AP4033386
chlorLde yielded a r~sLnILko polymer with TL-O-P backbone and pendant
butoxy- and mathyl groups* Orig, art. bast 2 figures,
ASSOCIATION1 ln#tLtut elementoorgauLcheekLkh soyedLnenty AN SSSR
(institute of OrSanoeleviental. Compounds, AN SSSR)
ISUBMITTEDt 278op62 DLTZ ACq i 151(ayG4 IINC161 01
SUB CODEt CH. WRIVOISOTS 002 OTHZR& 002
LCSrd 3 4