SCIENTIFIC ABSTRACT ANDREYEVA,I.B. - ANDREYEVA, I. Y.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R000101410002-2
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: March 20, 2001
• Sequence Number: 2
• Publication Date: December 31, 1967
• Content Type: SCIENCEAB

The Results of Seismic-Aooustic Expluration 2o-119-3-52/65
of the Bottom of the Japan Sea
depth of loo-6oo m. 2 pairs of Kpaographs directed
opposite (vatrechnyy) to each other were constructed
from the data on the entering of refracted waves and
data on the limit velocity of the sound as well as on
the depth of the refracting boundaries of the deeper
-seated ground la3ers. 2 layers with considerably diffe-
rent limit velocities in both cross sections could be
distinguishud. The velocities differed in both cross
sections. This difference seems to be due to measurinb.
errors and to the fact that the actual geological cona
ditions did not agree with the idealized assumptions
the computation-was based on. Apparently a basaltic
layer of a thickness of from 6-7 to 7-8 m is stratified
under the loose deposit. As it seems to the authors the
results prove the fact that a considerable mass of loose
ground deposits exists in the western part of the Ya-
ponskoye sea which is not separated by distinct boun.
daries. The change of ihe thickness of this layer is
obviously connected with the supply of deposits from
Card 3/4 the continent and with the relief of the subjacent

ANDREYEVAOI.B.: LISITSYN.,A.P.: lUD:INTSEVO G.B.: NEFROCHNOVIYU.P.: SYSCIEV,N.N.:
)ITIC101#11M, I.)M.
"Results of Seismo-Acoustic Irmestigations of the Ocean Bottom"
31-AUG 11 Sep 59
a paper presented at the international oceanographic congress , 31 aug--=e) ~9
-IL/
, A: w Yo ,C <
so; 73, 3, 142)129 22 )ct 59

FRASE I BOOK F-17LOITATIM SOV/5331
International Geological Congress. 21st, Copenhagen, 1960.
X*rskaya goc2oglya (Iffarlme Ooology) Moscow, Itd-vo AN 3.%Mns 1960.
205 p. 2,500 copies printed. (3erleas Dok2ady movetakLkh
geologoTs problema 10)
Zd1torial Boards P. L. bezrukuys Reap. Ed.; A. V. 2hivaZo. V. P.
Zenkovich and 0. B. Vdintsev; Ed. of Publiching Uouses V. S.
Sheynstan; Tech. Zd.s V. Karpov.
PURPOSEt Oda book is Intended for goo2ogisto and oceanographers.
COVERAdRs The book contains IS articles representing the roporto
given by Soviet goologlets at the 2lot. International GooloCleal
Congress. Individual articles deal with the bott4m tc*aZr.-Ay.
sedimentation, and t,"tonlea of oceans (W:5torn Facifto and
Southern Indian), to well an the Zoomor2holoZj and tectonics of
the Black and Conplass Benz and Soviet sectors of the Baltic.
An 7-01-h rdo=* accopDassise oach article. No personalities
X. W., I. Y.*. my-hax-t,eq!, 0. a.
llcitz7n, and J~. 1. Xoproclpv. 7FCR%Llto Of
tions -tfi--UiW a Crust Under
ountitSURG f a
Seas and Oceans 35
ftldov~ Sh K. StratIgraphi -Cf'Sediment.~ and the YaleorecCrs;4hy
OrtH. j.r torn Pacific and the Far Zr3tarn Seas of the
USSR According to Sea-Dottom Foraminifers 59
Formation of Sediments in the Southern
-Pacific and Indian Oceans 69
laplbj.-JE.P~.. and X. A Belay. Bottom Sedimentation Can.
M-no in ihe Are can 1 88
a t1V.PP_ and TO. F. Xpro6mov. Bottom aeactorphology
o-nMdUctatov. robleass of the black Sea 94
0 " V. V;' L 3 Mdakova and 0. V. A Relief and
HOMMAYP-31 ruVt~u;;. 105
Re on r
M
GerahanovIch D To Recent Shelf Depoolta in the X4xg1nv2
of.11W tn;x-
Seas
1& 116
a, The Oeo2ogr of the Barents Sea 123
Gorahkova, T. 1. Sediments In the Norwegian Sea 132
V. Study of the Diagenessiss of Some Marine
140
Zenkovich V F , 0 K Leontlyevp and To. it V vessak:y. The
-influence or &6irF-fo -ulaclal Tranc~Fosla n r4w
Development or the Coastal Zone of Soviet SeLs 154
bulatov, X. A., V. L @v and V 7 ZonkovIah. go"
l64
Budanov, V. Ii. A; 1. loan, 21n, and V. 3. Modvedev.
-4W" f the 8Zft6f-U=UrT- IT5
-He , Vert 0 1 vemsenta 0 Be orea
jXSv,0. X. Types and Formation of Lagoons a" Recent
3.29hores- IBU
Card-VJ&

ANDREYEVA, I.B.; CHINDONOVA, Yu.G.
- -
Nature of sound-scattering layers. Okeanologiia 4 no.IsII2-124
164, (MIRA 17:4)
1. Akustichoskiy institut AN SSSR.

ANDREYYEVA, I.B.
1.
Z-3cattering of sound by fish bladders in deep Bcattering layers
in the ocean. Akust. zhur. 10 no.ls20-24 164. (MIRA 17:5)
1. Akusticheskiy institut AN SSSR, Moskva.

t W(lVkW( _iAid'(0-4:
lk TJP 0 W/M
ACC Mi AP6011944 SOURCE CODE: UIVO2131651005100611-MA 07
AUTHM Androyqva 1. N
ORG:. Acoustics Institq~.j_hj~SSS& (Akusticheakiy institut AN SM)
TITLE: At,,-austic-characteristies of sound-scattering layers in the ocean and data 4~
of echo ounder observations anT-direct catches
SOURCE: Okeanologiya, v. 5, no. 6, 1965, 1028-1037
~TOPIC TAGS: acoustic scattering- acoustic wave,-ocean acoustics, sonar
ABSTRACT; In order to take into accourit-~he influence of sound-scattering
layers on the pr9pagition of acoiistic waves In the ocean it is necessary
to Mow their quantitative acoustic characteristics: intensity of the
layerp scattering coefficient and the depend,,;.-.ce of these parameters on
frequencr and depth. Data from echosounder observations can be ex-
t
re. onalization of lage ocean
mely effective both for a preliminary regi
-areas on the basis of the abundance of sound-scattering accumulations
,and for faci2-itating the regionalization made on the basis of the results
of quantitative acountic measurements. Hodern echo sounders, designed. '.1
for measuring ocean depths, cannot ensure measurement of the cluantitative''I
characteristics of sound-scattering layers ana therefore do not make
.poss-iblo even qualitative bvaluation of the degree and character or the
'influence of biological accumulations on the underwater propagation of
-sound. Relatively small changes and additions to depth sounder circuits.,,-
L_ Card 1& UDC: 577-472(26)

L 4b956-66 egl~j
ACC NRs AP603045( SOURCE CODE: UR/0213/66/oo6/oo4/o599/o6O7
AUTHOR: Andreveva. I. B.
ORG: Acoustic Institute (Akusticheskiy institut)
\V
TITLE: Study of volume sound scattering in the ocean and measurement of acoustic
characteristics of scattering layers
SOURCE: Okeemologiya, v. 6, no. 4, 1966, 599-607
TOPIC TAGS: acoustic scattering, acoustic detection, acoustic analysis, sbipborne,
acoustic detection, acoustic equipment, acoustic measurement, acoustic propagation,
underwater explosion, underwater acoustics, underwater sound equipment, ocean
acoustics, oceanography, volume sound scattering
ABSTRACT: The article describes the development and use of modifications of a method
of measuring the averaged acoustic characteristics of both the sound-scattering and.~h
surface-bubbling layers. Two types of experiments (see Figs. 1 and 2) were under-
taken to determine the characteristics of volume scattering. Two formulas are giveR-,
which serve as the initial computational relationships used in processing the experf4
mental data. The procedures followed in both experiments are outlined in detail, and
the methods and equipment used,in recording and processing shot data are described.
Two steps are followed in analyzing the experimental data. The first consists of
frequency selection with the output re-recorded on magnetic tape. The primary
Card I/q UDC: 551.463.262(26)
C"d..
Zt3-

L 46956-66
ACC NR, AP603t)456
(I V -, 4 4i e~~~er
Fig. 1. Setup of components in'-
experiment 1
1 - Recording mid control system;
2 - weight; 3 - hydrophone and
preamplifier; 4 - shot. .
layer
Fig. 2. Setup of''compone'nit's in
experiment 2
1 - Recording and control system;
2 - preamplifier; 3 - hydrophone;
4 - charges; 5 - weight; 6 - shot.
recording of each shot is filtered 8 to 10 times. In the second step, the secondary
recording is reproduced, amplified,.and detected. Using formulas given in the article

L- 4695
ACC AP603o456
3
and the detector outDut signal, scattering strength and the dependence of the
scattering coefficient on depth may be calculated mwiu&lly or by computer.* The
assistance of I. Ye. Mikhalltsev, Yu. Yu. Zhitkovskiy, and B. F. Kurlyanoy in
developing the deacribed technique is acknowledged. Orig. art. has: 12 formulas
and 6 figures. [LBI
SUB CODE: 08, 17, 19, 20/ SUBM DATE: 17ju165/ ORIG REF: oo6/ OTH REF: 0o8/
ATD PRESS: 5088
Card 3/3

ACC NRt jIF7000141 -~66i&i~-c-oi~i-.-6ii6-o-46/66/0'1'2-/00'4/-039~/o o4.
;'.AUTHOR: ~~l!!Xyj~k,I,..,,B.";,-Kharatlyan, Ye. G.
I-ORG: A*C-0*'Ustic natitute, AN GSBR, Moscow (Akusticheakiy institut AN SSSR)
TITLE: Sound sdattering by the ocean surface and by near-surface sound-scattering
layers
iSOURCE: Akusticheakiy zht!-
-nal, v. 12, no. 4, 1966, 399-ho4
TOPIC TAGS: scattering, aaand . grazing angle, oceanAPeG%%rP6u%,, acoustic
scLttering
The resultj of af .-,;,.,stigation ol- sound scattering by' the near,rface layers
u
of !:'he oce~v by the resea.-..h vessel "Hikhail Lomonosov" in the
Vist.ern e-j4at,,!.-..
rrigion of the Atl.~MtiC Ocean in September--Noverber 1963
art- described. Underwater explosioA-i served as acoustic sources, while a
c,.--.-qic sphere locate4 a short disttAce above them point of explosion was the
hydrophone.1 The depth of the wholf system was varied between 200 and 500 m.
The absolute values of the effectivo surface backscattering coefficients (a)
were dateralined from the recorded scattering. The frequency dependence of a
as well as [its variation with the grazing angle were also obtained within
the limits 'of 1-40 ke and 10-60', respectively. It was established that at
Card 1/2 _Vw; 534-24:551-46

ACC NRI APWOK~hl
grazing an es 688 than 30' and at frequencies of 3-10 kc, the scattering
field is termined primarily by volum scattering and not by scattering by
'Ifttif
nonhopogen ities of the air-water interface. At grazing angles greater than
30* and at frequencies of 1-2 ke and 10-40 cps, scattering is believed to
be caused 1by surface nonhomogeneities. Orig. art.. has: * 6 fomulas and'
4 figures.!
suB-com oe/ huBm DATE: O1jun65/ ORIG REF: 006/ M REF: OOT/ An PRESS: 5112
Lcqrd 2/2

s/i86/63/005/001/007/013
E075/E436
AUTHORS: I. B. Andreyov, P.P., Rogozina, E.M.
TITLE: Investigation of the processes and interaction products
of high molecular weight compounds with inorganic salts
II. Formation of complexes between poly (a-methyl)acrolein
and uranyl nitrate
PERIODICAL: Radiokhimiya, v-5, no.1, 1963, 103-1o6
,TEXT: Polymerization of (a-methyl)acrolein was carried out with
different catalysts to investigate the influence of substituents
in the a position on "be ability of the polymer to complex with
U02(NO3)2- Ethyl-, propyl- and butyl-acroleins were also
synthesized but could only be polymerized with metallic Na.
Details of the polymerization procedures will be reported
separately. Poly(a-methyl)acroleins obtained by emulsion
:.polymerization with AgN03 and K2SO5 Mohr's salt and K2SO5,
6
hyposulfite and K2SO5.absorbed 1000 x 10- go U per g of polymer.
Auto-polymerized polymer absorbed 2000 x 10-9 g of U per g of
polymer, its content of aldehyde groups being of the same order
(66 to 69 mo.1%) as in the previous polymers. The polymers
Card 1/2

s/i86/63/005/001/007/013
Investigation of the processes ... E075/E436
obtained in the presence of BF3, lithium-butyl and Na contained
only 9 to 12% aldehyde groups and did not complex with U. The.
complex formation took place to the greatest extent at the pil
values of 3 to 4. In general the presence of inethyl gr-)ups in
the polyiner makes it hydrophobic and less capable of complexing
with U than polyacrololn. There are I figure and 1 table.
SUBMITTED: January 3, 1962
Card 2/2

ANDREYEVA I. F. I ZUBKOVICH, L.E.
=L~-
19856 ANDREYEWVA, I. F. i ZUBKOVICHp L. E., Svoystva karbogidraz v sozrevayushehem
zeme pshenitsy i sintez krakhmalInykh zeren vne zhevoy kletad. Biokhemiya, 1949,,
Vyp- 3, s. 249-55. -Bibllogr: 7 nazv.
SO: LETOPIS ZHURNAL STATEY, Vol. 27, MOSKVA, 1949.

ANDREYEVA, I.I.
Rhythm of the seasonal developmant of plants in the mixed beeoh and
chestnut forests of the Batum seashore of the Caucasus. Biul. Glav.
bot. sada no.51%67-77 163. (MA 17:2)
?c 3dagogicheskiy institut imemi Lenina, Moskva.

ANDRNYEVA, I.I.
Shoot formation and the rhythm of seasonal development of the
same species in Moscow Province and on the Butum shore. Biul.
Glav. bot. sada no-54:9-16 164.
(MIRA 17:11)
It Moskovokiy gosudarstvennyY pedagogichaskiy institut imeni Lenina.

SOURGH CODSt
66o/bl3/bo5q/0O5O
ACC NR, Ap60j560� f4 To~~1661
DWIMORSt Volkov) So No; Makarlinp Vo Poj Falevich, K. X.; Rubaylo, G. ft.;
Gorasimova,j~._4,j Fqazantaeva, Vs Mq Andrey Semenova, A* Go
ORGi none
TITLE; A machine for contact spot welding. Mass 21p No. 183300
SOURCE: Izobrateniyas pronyahlennge obraztey, toyarnyye znaki, no. 13) 1966, 50
TOPIC-TAGS: welding, spot welding, welding technolo y, welding equipment
ABSTRAM This Author Certificate presents a machine for contact spot welding.
'the machine contains a frame and welding transformers, each of which is electrically
connected to a group of welding guns (see Figo I)o To increase the productivity,
the welding transformers together with.the corresponding group of welding guns are
mounted on the vertical planes of plates which move under the action of a driving
mechanism located on the frame. The movement takes place along the horizontal
guides also located on the frameo Rods attached to one of the plates serve as
auxiliary pides for awther plate. These rods are intended for fixing the plates
Card 1/2
I=t 421-701-M.I.nT

ACC
Fig. 1e I - welding transformeraj 2 - welding
gunn 3 wA 4 - vertical"platsai - driving
machanim for plates; 6 fr"ej 7 - guides;
rod*
in their original posit..-. -_-7.~or to w&Uingo. OrIS6 arU hass I figure.
S" CODII 231 SM DVI# 16hrAS

ANDREYETA, I.M.,; IVANOV, I.T.
Use of semiconductor diodes for electric frequency control in
oup6rbigh-frequenoy cavity resonators. Vest.Mosk,,un. Serjt
Fiz.,,astron. 17 no.613-6 N-D 162. (MIRA 15a12)
1. Kafedra teorii kolebaniy Hoskovskogo universiteta.
(Electric resonators) (Diodes)

ALEKSANDROVA, L.N,; ANDRMVA, I.M.
Transformation of humus substances in the soil. Pochvovedanie
nc).7:20-26 JI '63, (MIRA 164)
1. Leningradskiy sellskokh-ozyaystveWi5,y institut.
(Humus)
w

KAGAN, D.F., kand. tekhn.nauk; VANYAXIN, D.M., kand. tolckn, nank;
LOUCREV; F.V., kand, tekhn. nauk; YEKNUKOV, S.V., inzh.j
PAVLOV, L.D., inzh.; RUZINq M.Yn,., inzh.; ANDMEVA, I.N.,
inzh.; SHMOVA, G.D... inzh. Prininali Mucga~stiye.
SAPOZENIKOV, M.M.j kand. tekhn. nauk; GEFDING, A.K., kand.
teklm. nauk; MAUIOVSKIY, H.B.p inzh.; STRASWO, V.P.p
red. izd-va; W3MOV, D.Ya.s tekhn. red,
[Instructions for designing, installing, operating, and
repairing interior water supply systems using vinyl plastic
pipes) Ukazaniia po proektirovaniiu,, wontazhu, ekspluatatsii
i remontu vnutrennikh vodoprovodov iz viniplastovykh trub.
Moekva; Goa. izd-vo lit-ry po stroit., arkhit. i stroit. mi-
terialam, 1961. 91 p. (MIRA .15.-2)
1. Akademiya stroitel'stva i arkhitektury SSSR. Institut sa-
ni-FArnoy tekhniki. 2. Nauchno-isoledovatellskiy institut sa-
nitarnoy tekhniki Akademii stroitel'stva i arkhitektury SSSR
(for Kagan, Vanyakin, Lobachev, Yekhlakov, Pavlov, Ruzin,
Androyeva., Shmakova). 3. Leningradskiy nauchno-iB'sledovatellaidy
institut AAademiJ kommunallnogo khozyaystva in. K.D.Pamfilava
(for Sapozhnikov). 4. Vaegoyuznyy nauohno-insledovatel'okly in-
stitut gidrotakhnichoskikh i qanitarno-tekhnicheskikb rabot
(for Gefding). 5, Institut po proyektirovaniyu zbilisholmo-
grazhdanskogo stroitel'stva V.5. MoDkve (for Malinovskiy).
(Water..pipe

. -IT-
A~ --I
ANDREMNA, 1. N. "Detemination of Gonstan-~s of the Vigration of
a Chain of Organic Compounds in the Initiated PolynierizatJon of !b-thyl
Metacrylate." Min Higher Education USSR. Leningrad ()rder of Labor Red
Banner 7echnological In:31,-, imeni Leningrad Soviet. Chair of the 'reclinology
of Plastics. Leningrad, 1955. (Dissertation for the Derrme of Candidate in
Chemical Sciences)
SOURCE Kn1zhnaya Letopis', 'mo 6 1956

AM 0 R E'Y F- Y141 ~T-, 1Y,
YEGOROV, N.Me; AMIPOVA, Z.V.; VBSBWVSKAYA,, Yaj.; IJCVINA, A.A.; SIMOTA,
A.&,;.3MAVSKIY, A.Ge; ADMITIVAg I*N*
Gyalic and continuous methods for the polymerization of ethylene
at low.pressures.-Khim. nauka i prom. 2 no-3098-399 157,
-- _i I" iy ins' WRA. 10:8)
1. Hauchno-iseledovate sk titut polimerizatsionnykh plastuass,
(Ithylens (Pblymerization)~

RtORF-YEVA, I-W
50) P. PHASE I BOOK ECEWITATION SM11639
Polietilen nizkogo dayleni" (Im-~resoure'Plolqethylene) laningrad
Goskfilmizdat,, 1958, 90 p. (Series: Novyye plastichepkiye mwly~ 10,0W
copies printed.
Ed. (Title page)- N.M. Yegorov; Ed, (Inside book)t Ye. T. Shur;
., Tech. Ed.: Ye. Ye. Irlikh.
PW.1039: This booklet is intended for sechanicii engineers and 1,echnicians in
chemistry., petroleizm technology, foods., pharmaceuticals, electrical enginearingi,
battery manufacturing, radio engineering, automobile manufacturing, - hifilb;; .
frequency engineering, televisions ommmicationss machine- and ihiV-bftild1ngp
aviation, construction and other branches of industry empioying plastic
materials.
COVERAW: Thar booklet deseribes a nev mater:L4.- polyethyle.ne-produced at low
pressures. ' Its industrial preparation and properties are deseribed along with
rbethods of taking articles from this material and its application in building
technology, medicine and other branches of science, The booklet vas compiled
by personnel of the Scientific Research Institute for Polymerized Plastics.,
Ch. I.: I.11. Andreyeva, Z.V. Arkhtpovs, Ye,V. Veselovskaya, AA, JAvina;
CardlA

I.ow-pressure, Polyethylene sov/1639
Resistivity and electric strength
Aging of low-pressure polyethylene
30
Ch. III. Manufacture of Polyethylene Articles and Their Fields of
Application 55
Die caiting 50
Extrusion method of processing 61
Coating of conductors with polyethylene insulation 70
Processing low-pressure polyethylene by press forming 71
Applying protective coatings of low-pressure polyethylene to
metal parts by fusion 76
Welding plates and pipes of low-pressure polyethylene and the
formation of sheets (bending operations) 77
Welding sheets and plates 78
Welding pipes and welding-on flanges 80
Making T-Joints by velding pipes at right angles 83
length-irise weldiT* of tubing from sheets of low-pressure
polyethylene for ventilation and other purposes 84
]L-ndbg low-pressure polyethylene sheets and plates to a given angle 86
Welding low-pressure polyethylene parts with a rod and employing a
stream of hot air or nitrogen 87
Card 3/4

ANMN"74 A,LII.-;-ARKHIPOVA. Z.V.; VASSLOVSEAYA, Ye.Y.; UVINA, A.A.;
ANTOKOLISKAYA, U.N.; LAZAREVA, K.P.; SAMIN, B.I.; KRINIKIS,
S.S.; SHCHEREAK, P.H.; GERBILISKIY, I.S.; LYANDZMG, G.Ya.;
PARMORKOVA, T.V.; PHOHERKIN, A.L.; INGOROV, Y.M., red.;
MM, Ye.I., red.; POMKINA, T.A.. tekhn.red.
[Lov-pressure polyethylene] rolietilen nizkogo davleniia.
Izd.2.& lepr. i dop. Leningrad, Goe.nauchno-tekhn.izd-vo
khim.lit-ry. 1960. 95 p. (MIRA 14.-1)
1. Nauchno-issledovatel'skiy inatitut polimeri2atsionnykh plast-
mass (for all, except Yegorov, Shur, Pomkina).
('Pol~athylene)

EWT(z)/9PF(c)/EWP(J)j;~1' RPL W)~M
M
L 3913,-
AP5024496 UR/0191/651000101010OQ4/0006
ACCMSION NR:
4'~' ~< 678. 742. 2-134. 24:678. 044:547. 419A
N. Z able
AUTHOP- An_dreyeva. tual, V, ---M Seyergvg. N.
v, 7 7
V t1
Cq' 'iihylene (with p
#nTLV WlXnerizalt6n using certain 6rgat-omkill
catalysto
SOURCE: Plasticheskiye massy, no. 10, 1965, 4-6
'a
TOPICTAGS- ethylene, propylene, copolymerization, catalytic polymerization,
polymerization rate, copoly,::aer, polymerization catalyst, organoaluminum com-~,,
pound
ADMIACT: The relative activity of ethylent~- and propylene in their copolymeriii
y s'
tion using Ziegler;-NattaS died to obtain data necessary for the,
1~as Stu.
-%Ljl Sts
t ve
perties. The rela i
production of copolymers. having valuable technical p,~d,
activity. of propylene during copolymer-1 zation w1t4.0ift~:re6t ~,aialyst.sy~teMs'
i~~ creased Inj-he folloviing;-Order. + TIC14; (2~Al(
(1) AUCA )2Cl C2lI5)3.+ TIM
5 1 . 4
(3) A1(C2H -13 + VOC13-; (4) Al(C H5)2C1 +V. -=13; and, (5) AI(C2"5)3 + IX -TiCl
5 2 30:
Change In catalyst concentration had no effect on the activity of the monomers.
hange in the ratio of catalyst components in catalysts (4) and (5) did not chealge
Card 1/2

17 L 3912-66 -
ACCESSION NR, AP5024496,
the composition of the copolymer, but decrease in the ratio of the aluminum alkyl
in the other catalyst systems led to an increase in the propylene content in the
copolymer made with catalysts (1) and (2), and a decrease in propylene when us-.
ing catalyst (3). The copolymerization constants have the same values when ca-
talyst systems (4) or (5) ar6 used or when the Al(C6Hl3)3 + K -TiC13 system is
used, indicating that different'aluminum alkyl derivatives in combination with
V - TiC13 do not change the. relative activity of the monomers. Thecopolymeriza
tion constants change significantly with a change in the aluminum organic deriva-_
tives in systems based on Tidl4, This Is apparently due to the different reductf-
vility of the aluminum, organic derivatives and subsequent formation of different-.,
active centers. Orill. art. htis., 2 tables, 1 figure and 2 equations.
ASSOCIATION: None
SUBMITTED: 00 ENCL: 00 SUB CODE! OCI MT
SOV.- 002-._,.~" '_ -0 ER. 004 t '14
i?
Car 2

7
AIZA
4WEM OMIN
7 -7:-
-'R-PT.; Ww vu
PR:
~j -TrXLE: of an eZhyleni
propylene tqp_OU_~
mer
uw- 1965 9' 127,
Pra-st, C 11AUye iWSSy0_A
a- c0 yme -s 'thesis- -'poly
TOPIC TAGS -pihilene: cdp~lymer. 'POI. rp~
_,:,V;c?pyie-n polyolefin: yn
mer structure, p6lydi3persity, Zieglir.catalyst, polymer fractionation, Polymer
-molecular- weight
f--- ---
--in the-presenm-o a
p~hne' fii d-
'_ABSEVRACre. -Ethylitne. -_-ware_6olution~p yme a
n to aw-dy- the molecular weight distribution, COM o ition~
Ziegler-catalystj order - I P 8
and intrinsic vi6covity ofthe.copolymer and the mutual effects of molecular
weight and viscosity. The monamers were polymerized at 4-5 atm. with triethyla-
luminum-titanium tetrachloridet'o form a copolymer containing 4-10 mol.% propy-I-
lene, determined ' apectrographically from the methyl group concentrations.
The intrinsic viscosity was mangured in decalin solution on a capillary viscome-
ter- at 135C, the weight -average molecular weight was'datermined with an optical

77
------ ------
-44 0 C ------------
4t- j
tj J"01-~ellt aj~~-t tkilin
h- ti
ion wi to that of low pressure--P0
by precipitat to be a imilar
jar weight distribution va own. ctoril- by Tung's distribution functions
ethylene and to be described satisfa 7 molecular weight of the fractio
Wourn. Polymer Science v. 241,19.57, 333). The ns
decreased with increasing.content of propylene links. Fractionation was t;hown
to proceed both by copolymer Icomposition -and by molecular weight. The studied
did-not _indtcate a dii Ict de-efidence-of molecular weight-on intrinsic'.
--specimen e p
_isoodity,,--and --latte -,ParoLmetAi~is.,nof---recommenied for determining tile mole
-+
v
lar in this ty e:, of ~~opqjymer'#-. Or S'., ar
u -weight
c

I
ASSOCIATION,: :., vone
Zj

06
JD_ 9
.00
SUEHMED
4t
OTMt 005 77
- No REv-sovi -003
7,
- J
M4 V4

-ACC NR, A1'6(i2~65~- F-uft/o4l3-/6-6/o,)o/014/0050/0081
INVENTORS: Kuznetsov, Y06 Vs; Gusev, V. I.; Zhi4kova, T. N.1 Andreyeva, I. no;
Somenovap L. S..
ORG; none
TITLE: A motaod for obtaWng copolymers of propyleno. 01ass 39, No. 183938
SgtJR(;E-. Izobret prom obraz tov zn, no. lh, 1966, 60-81
TOPIC TAGSt polyiner,, copolymer, propylone, polyinerization, ester, phosphoric acid.,
catalyst, titanium compound, compound
ABSTRACT: This Author Certificate presents a ~.~Dhod for obtaining copolymers of
propylene with unsaturated compounds in the medium of an inert carbonaceous solvent
at the temperature from 20 to 60C. The process is carried out in the presence of a
catalyst consisting of titanipm tetrachloride and aluminum alkyls. To impart the
property of fire resistance to the copolymers, unsaturated mixed esters of phosphoric
acid are used as the unsaturated compounds,
SUB CODE: ll/ SUB14 DATE: 06Sep62
0
UDC.- 678.

ANDREYEVA, I.N.I,ZAPLETNYAK, V.M.1 SEVEROVA, N.N.; ARKHIPOVA, Z.V.
Copolymerization of ethylene and propylene with the use of some
organometallie catalysts. Plast. massy no.10:4-6 165.
(MIRA 18:10)

1. Ti.
GINULI, ?.A.; ANDREVIVA, I.N.; YXMAKOVA, K.G.; TSVrGTKOVA,
Xffect CT the-newti'llage system on the basic features in the
physiology of wheat* Isy. AN SSSR. Ser.biol. no.4:44V465 Jl-Ag '57-
(KLRA 10:8)
1. Institut fisiologii rastenty Im, I.A.Timiryateva Akedemit nauk
SSSR.
(TIIJAGB) (WHIIAT)

AOFI~'VA.p I.N.
Plant nutrition as influenced by T.S. Malitsev's new tillage system
[with summary In ftlighl, liziol. rast. 4 no.6.'533-541 X-D 157.
(MIRA lOt12)
1, Institut fitiologii rasteniy Im. K.A. Timiryazeva AN SSSR. Xoskva.
(Tillage) (Plants--Nutrition)

NDREyEvA, _IL-,-Oand Biol Svi (dies) "Peculiarities of nutrition
A 41
of plants unde r now system of treatment of soil. fteovvA -ing-066 W-e-T
Physio
I"al-tsev jVt%WpO 1joa, 1958.. 20 pp (Inst oi logy of Plante
im K. A. Timiryazev, Pcaa Sci USSR), 150 copies (KL, 13-58, 106)
-/F-

OMTRY USSR
CAT3XVRY Plant Physiology. Mineral Ilutrition.
B5. JOUR.~ i RM161.0 No. 6 ~959,o No- 24533
: Andreyeva, 1.11.
S -
TITLE Gharagteristios of Plant Nutrition Under the New
r;yatem of Soil Wtivation of T. S. Malltsev
OZG- PUB-- t P1ziol-.rast6ni7-q 19571 4, No. 6t 533-541
BSTRACT t In fields on the collective farm "Zavat Illichall
and in the Shadrinskiy Rayon experimental station
of. Mrganekeya oblesti, for the purpose of
soientifioally testing the new system of soil
cultivation of To So Valltser I a system of
mineral nutrition of corn and sunflower vms studied
by determining the composition of the plant juices
by the Sabinin method (Biol. otd. semled., 1928,
No. 15). It has been established that the method
of diagnosing mineral nutrition by analysis of the
1/2
11

GENKELI, P.A., prof.; ANDREYEVA,..1 ., kand.biologicheakikh nauk
"j(
Now scientific data on cellular structure. Biol.v shkole
no.6t83-88 N-D 162. (MIRA 16W
1. Institut fisiologii rastenly imeni K.A*Timiz7azfva AN SWR.
(COUS) (Electron microscopy)

ANDREYEVA, I.N.
Absorption of mineral substances by plants subjected to a
desiccant wind. Fiziol. rast. 11 no.1:79-86 Ja-F 164.
(MIRA' 17:2)
1. Institut fiziologii rasteniy imeni K.A. Timiryazeva AN
SSSR, Moskva.

Oxidative phoophor-y3Ation in the mitochondria
Fiziol.rast. 12 no-4215,84-590 JI-Ag 165,,
1. Institut fiziologit
Moskva. Submitted June
(MIRA 1802)
K.A.Timiryazeva AN SSSR,

A1TD1--ZF%VA-)- - I.- - P.-
nInvestigation of Irregular Operation of Hydroelectric Station Aggregates."
M;scow Order of Lenin Power Engineering Inst imeni V. M. Molotov, Min Higher
Education USSR, Moscow, 1955. (KL, No 14, Apr 55)
SO: Sum. No. 704, 2 Nov 55 - Survey of Scientific and Technical Dissertations Defended
at USSR Higher Ed-ccational Institutions (16).

-F, W-
ANDRUIVA, I.P., kandidat takhnichaskikh nauk,
StalAlity of steady states in hydroelectric power stations and
power systems. Tr*r NEI no.19:95-105 156. (MIRA IM-1)
1. Xafe&ra gidroonergetiki.
(Pbwer engineering)
TV

ANDRMTVA, 1. S.
-
"Anatomiconorphological and Biochanical Character of Pears with Different Rates of
Ripening." Cand Agr Sci, Fruit and Vegetable Inst imeni 1. V. Michurin, Min Higher
Education USSR, Michurinsk, 1954. (KLI 140 17, Apr 55)
SO: Sum. No. 704, 2 Nov 55 - Survey of Scientific and Tec1mical Dissertations Defended
at USSR Higher Educational Institutions (16).

ANDRrMA, I.S., kand.sel'ekokhozyaystvannykh nauk
The ability of pear to take root from green cuttings.
AgrobiologRa no.1:146-147 Ja-F 159. (MIRA 12:4)
1. Baratovskly sellskokhosysystvenzily institut.
Mari

ANDREMA.. I.S.
Anatomic structure of Acanthopanax sessiliflorum Seem. Soob. MAN
SSSR no.18s67-72 163. (MIRA 17:11)
1. Dallnerostochnyy filial imeni Komarova Sibirskogo otdeleniya AN
SSSR.

ANDREYEVA I S
Anatomical characteristics of ginseng roots of various age. Mat.
k izuch. zhen'shenia, i lim. no-4:216-M 160. (MIRA 13:9)
1. DallnevostochM filial Sibirskogo otdelaniya AN SSSR.
(GINsENQ (ROOTS (BOTANY)-4HATOMY)

ANMYEVA
Comparative microohomioal study of plarits of the ginseng famJ17 in
the Far East. Mat. k izuoh. zhen'shenia i lim.,no.4t222-224 160.
(MIRA 13:9)
1. Dalinevostoohnyy filial Sibirskogo otdeleniya, AN SSSR.
(SOVIET FAR EAST-GINSENG) (GLYCOSID.&S)

.-ANDREYEVA, I.S.
Some anatomical characteristics of Eleutherococcus sentioocus Bax.
Soob.DVFAN SSSR no. 15:135-138 162. (PIRA DO)
1. Dallnevostochnyy filial Sibirskogo otdelenlya AN SSSR.

ISAYEVA, Z.G.; An_
Int'eraction of 4 3 -carene oxide-with.methyl alcohQl.in the
-prenance-of-sodium methylate. ..Dokl. AN SSSR 152 no.2-34-2-
345.S 163. (kRA 16 M)
1. Nauchno-:Lsaledovateliskiy kbimiche-skiy institut im.A.M.Butlerova
pri Kazanskom gosudarstvennom universiteteim. VJ. Ullyanova-
Lenina. Predstavleno akademikom B.A. Arbuzovym.

ISAYEVA, Z.G.; ANDREYEVA,_I.-S.
Isomerization of 4 3 -carene oxide in the reaction with alcohols
in the presence of acids. Dokl. AN SSSR 152 no.1:106-109 S
163. (MIRA 160)
1. Nauchno-issledovateltakiy khimichaskiy institut im. A.M.Butlerova
Kazanskogo gosudarstvennogo universiteta. im. Ullyanova-lanina.
Predstavleno akademikom B.A.Arbuzovym.
(Carene) (Alcohols) (Isomerization)

ANDREYEVA, I.S.
Dynamics of the reserve substances of ginseng during the vege-
tative period. Hat. k izuch. zhen'. i drug. 2ek. rast. Dal'.
Vost, no.5W-52 163.
Anatomic and microchemical characterittics of the roots of
ginro4g, from distant regions. lbid.t63-67 (MIRA 170)
1. Pallnevestt-chayy f1lia-I Iment Xomarova Sibirakogo otdoleniya
AN &SM.

ARBUZOV, B.A.; ISAYEVA, Z.G.; AIIDREYF.VA, I.S.
Isomerization of OL-pinene and,43-carene oxides with lithium di-
ethylamine. Izv. AN SSSR. Ser. khim. no.5:838-843 165. (MIRA 18:5)
1. Nauohno-issledovateltakiy khimicheakiy institut im. A.M.Butlerova
Kazanskogo gosudarstvannogo universiteta im. V.I.Ullyanova-Lenina.

-) -T.---T. - - - - -- --- - --- -- -
1420 Tasladova.lye napr-yazhennly v tallindrakh UldravItcheskikh pressov. M., 1954
8 a. 19 sm. (M-vo vyssh. obrAzovaniya SSSR. Moak. stankoinstrum. In-t im. I. V.
Stalina). 100 ekz. Bespl. -(54-53768)
SO: Knizhaya Letopis', Vol. 1, 1955

77-
520-4 ~: I -
-(z)/EWP _HH-_
rA -
~56 W
ACC_kks_' AP6001658 SOURGE CODE3 UHTow_07g;w~/O-i2 2039/2047~
AUTHORSt Kot6n. M. H.j. reveyg. 11 V Getmanchuk. )L~U P.; ttadMkaYaj_L.'YaL1
Pokrovskiy, Ye. I.; Ko ItSov, A. 1.sjxl~mbovat V. A.
ORG: Institute of Huh-Molecular Polymers AN SM (Institut vysokomolakulyarnYkh,
soyed Y AN SSSR)
TITLEt Structure of nethacroleintpolymeraj obtained in the presence of anionic
cataly;0tv, 3rd rep.ort--i'on-tl-i-e-,rer-ie~i~Polyuierization of Acrolein and Its Derivatives
SOUR~Et Vysokomolokulyarnyye soyedineniya., Y. 7. no. 12, 1965, 2039-2041
TOPIC TAGSt polymerization, polymer structure,, reaction machanism, caW-,'y stl Nippon
Bunko infrared spectrophotometer DS 301) GNM 3 nuclear magnetic resonance.spectrometer
ABSTRAM The structure of.polymers obtained from methacrolein and 6( -ethyla~crolein
in the presence of sodium naphthalene and sodium trityl -Asing the method described
by M. M. Koton, 1. V. Andreyevai and Yu. P. Getmanchuk (Dokl. AN SSSR, 155, 836,~ 1964
was investigated. -The structure analysis was performed by chemical meanst~, oxime
formation. hydrogenation, 9xidation with perbenzoic, acid,, ozonization, as well as
physical meanst infrared spectra, using Nippon-Bunko spectrophotometer DS-301, and
NMR spectra, using instrument GNM-3, It was established that the rate of conversion
of methacrolein &nd the structure of the obtained polymer are both functions of the qj~
polymerization tsVzi-ature, as illustrated in Fig. 1e Mechanism of the polymerizatibn
I Card L113 UDCa 678-01t53+67 0744

L 13082-66 HW(m)1EWP(J)1T Hff
ACC NR: AP6002215 SOURCE COM UR/0080/65/038/012/2740/2744~
iAUTHOR: Andreyeva, I. Yjs KQto
~nM. ~M. GqtmancbA;k Tarasova,
IORG: Institute of High Molecular Compounds, AN SSSR (Institut vysckomo1.ekulyArnY
'soedinenTy-ANSSSR)
IVA
TITLE: Emulsion riz
-pol atio of methacrolein
iSOURCE:' Zhurnal prikladnoy khimii, v. 38, no. 12, 1965, 2740-2744
..-ITOPIC TAGS- emulsion polymerization, methacroleiri, catalytic.polymerization, high
polymer, polymerp acrylic plastic
P.
IABSTRACT: Emulsion polymerization of methacrolein was studied in the presence of
-1
ipotassium persulfate and.silver nitrafe*-w,ith a solution of polyacrolein bisulfite as,
la apecific emulsifier. The object of the workwas to develop a process for making a
Asoluble polymer with high molecular weight containing reactive aldebyde groups, The
optimum ratio of the monomer to water Is 1:8 and the optimum polymerization tempera-:
turo is 500 C. In all experiments the emulsifier content was constant (5 wt % based
ion the monomer). The pmount of the initiator varied but the ratio of silver nitrate
4,1
UDCitli78.74

L -13082-&
!ACC NR: AIP6002215
f
at

W
at
70 -
df

L 6__B
Fig. 2. The effect of solution pH
on
Z 4 6 polyacrolein characteristic vlscosity~q
and polymer yield for 6 hr polymeriza-
Fig. 1. Polyacrolein characteristic vis- tion and K2S208:AgNO3 ratio of 0.6:0.0
q
cosity n asa function of polymerization ,
mole
duration. A characteristic viscosity q;
-in
B~- is polymerizdtion duration hours;
A - n; B percent conversion; V.- ini-
the ratio of K2S208 to AgNOS:in mole'%; tial solution pH; 1 polyacrolein
I - 0.6:0,06; 2 - 0o6:0.06 (in presenoe of yield in percent; 2 polymer charac-.
a buffer)q 3 and 4 1.3:0.13; 5 2*6t teristic viscosity q.
3
_

0;O0006geo0o off 09 o a "1 9 0
I " a
a I I _11,_ 11 1 - I I IV It
L Al A f.
A A- A Al-I
A
.4 Pi-0.91st
go. F pelf 'EVOWICS -6f.
0
goes* 000000000001W
0
I A-
0 A 0
orliol.__
fol
,-The gynthells of viliefa 9( thr- 1,3-dicialkiro- &ad -df-
. Andrveva still I.- N.
.
tromakyoldne of I. N
"
so Ir t, I ,
SNUmlim Vormir.-h. GosudaW,
chrinov. val MCA .
Wly
so t Org, Kkim. 1193fl. Pi. 1. 73 %1: KAim.

dividestshyddo wims.A.talard Nora AeCl six) the ilk loto-
-mi
s
t w
P0%
h
d
ld
f
l
t.
a
o
e ctsk
e pro
uc
t
apt
hydrin, The Vir
and that to( the purv product dirpmc 00% bit 1q4. 1mr,
$ 1
4571. Utz esttr (as well as all o1her
it
4"
mV 1
.
.
.
,
raQy Vol. In MeM 1
in tmnlctw and water
eActs) I- Instol
;
,
still U1011. AcONt. CIICIa samal other lotti. sialyttits. The
drio% wiv% o1stainell with sk
oomb
ven4 d1hi
t
l
t
t
avor
i
ield t
e ti
s
-v
)
A
took 11t$'
of crude or "N" tal
tuiv Illodlit'j
of Sl
y
11 1
d ,
.
,v
I
.879, and ms%r 1.5141. 1rhe v iltnuoicrtate of t1yettol
4 .
dichl urroloydrin was obtained front the dirldofohydTin still
cielItCOM 'nif Yield W t Ito rate potoduct WAA 71 %,
b. W-41" ago I 'At poll 1 4AM The chlottucctiall, A
k`ha was :411jahard Its a milliho 1.
l
evrol JIQM,ji~
a
r
~d
The yiehl *Av:bL,O%. Ili, " 1113", ilk, 2 146. 10%,1
It was not poomalble to symbesize the bv;~tlat. .4 gly'l-tol
dichlam- or dibrorwhydrin. W R~ Mean

AIMLUWGKI~ 11MItOf CWIWKAT"
s-ft. 11*-.-A,,%;-
/-1 islesi) "it "v Got 414131CON-11 boliall OK Olkv ask
AM L
U 0 AV 10 1311, 0 1
0 0 0 0 0 4
-00
.00
000
'00
see
400
see
its 0
coo

ANTJUw-TwVAY I. V*
ANDREYEVA, I. V.--IrIU Synthesis and Polymerization of ViVl Deriva-
tives of the Furane and Thiophene Series." Acad Sci USSR.
Inst of &-gh-Moleculw.- Compounds. Leningrad,, 1955.
(Dissertation for the Degree of Candiate in Chemical
Science).
60 Knizhnaya letopial
No 2, 1956.

15-57-10-14441
Translation from: Referativnyy zhurnal, Geologlya, 1957, Nr 10,
p 177 (USSR)
AUTHORS: Andreyev, P. F., Andreyeva, I. V
TITLE: The Internal Structure ot Paraffin Oils (K voprosu o
vnutrennem stroyenii parafinistykh neftey)
PERIODICAL: Tr. Vses. neft. n.-i. geologorazved. in-ta, 1956,
Nr 95, pp 355-383.
ABSTRACT: Paraffin oil is believed to be a system consisting of
a dispersing medium (liquid hydrocarbons) and a dis-
persed phase (heavy tarry substances and solid hydro-
carbons). The materials of the dispersed phase ere
capable of mutual adsorption and formation of complex
Card 1/1 aggregates. G. A. Gladysaeva

Ueu WN".
VIM
v
I A,,J--...nJ '%I V
raie-n- ht ilid-
indimitcri ttmus. the aciivation enerrv fw iwt~ojdf- catak.
Id Im Itill:,

-- .. -- !~~! 1,-11. Tt-'~~t tt~41

YUAYk --I-X---KOTON, X.M.
Synthesis of vinvl derivatives of the furan series. Zhur. ob, khIIC
27 n.o.3-.671-677.mr '57. (NLRL 10:61
1. Institut vyookomolei:~IiarnAh soyedineniy Akad'smii nauk SSSR.
(Puran) (Vinyl compounds)

DI 4Z4j/'4E-Dc (j 4 E 3J
~11) and
.ix~ut A) II.Api-I 74 71j! 1.66m. I ills J;)rr-iexaL)IV ill fit(.
cn de statc It) improve thr i,-I I 'x Lj~ Cal
gave tile o,rtr,.I.)Fjtil g c".11kall"I to'l l'.1.,l,-d
VIA-lig 1" file A

AUTHORS: Andreyeva, I. V., Koton, M. M. 706-32-5-4/47
TITLE: The Influence of the Structure of Monomers on the Polymeriza-
bility in the Series of Vinyl Derivatives of Furan (Vliyaniye
stroyeniya monomer~,v na sposobnost' k polimerizatsii v ryadu
vin.illnykh proizvod-nykh furana)
PERIODICAL: Zhurnal fizicheskoy khimii, 1958, Vol. 32, Nr 5, PP. 991-994
('USSR)
ABSTRADT: The influence of the increase in number of condensed benzene
k ~ngs in the initial monomers on the polymerizability and on
some other properties was investigated; for this purpose "-
-vinylfuran, 2-vinylbenzofuran and 2--vinyldibenzofuran were
synthetized. In the determination of the polymerization kine-
tics in the block close to the benzoylperoxide a modified -
mercury dilatometer according to L.I. Yefimov was used, while
in using ionic catalysts a catalyst according to Schlenk was
taken. The characteristic viscosity and heat resistance of the
investigated Dolymers were determined by the IFL instrument-and are
given on Table 29 together with the obtained values
of activa-,'Lon energies. From the experimental results obtained
C&rd 1/2 can be seen that the velocity of polymerization in the series

The Influence of the Structure of Monomers on the 76-32-5-4/47
Polymerizability in the Series of Vinyl Derivatives of Puran
of 2--vinyldibenzofuran- 2-vinylbenzofuran- 2--vinylfuran in-
creases which is in agreement with the obtained values for the
aotivation energies; it was also observed in the case of
using an ionic oatalyat. In the same order also an increase of
the molecular weight and of the heat resistance of the corres-
ponding polymers was observed, a..-. well as an improvement of the
dielectric properties, which corresponds to the data of refer-
ences and to the data obtained. There are 6 figures, 2 tables,
and 5 references, 3 of which are Soviet.
ASSOCIATION: Akademiya nauk SSSR)Institut vysokomolelculyarnykh soyedineniy
(Institute of High-Molecular Compounds )AS USSR)
SUBMITTED: June 19, 1956
.1, Fi-ran derivatives--Polynterizatior, 2. Vinyl compounds
(Pol,Yme--ized) 3. Viul compound s- --Chemical reactioi)s
Card 2/2

AUTHORS: Anareyeva, I. V., Kotoni M. M. SOV/76-32-8-19/37
TITLE: The Effect of.,the Monomer Structure on the Polymerizability of
Vinyl Derivatives of Thiophene (Vliyaniye stroypniya monomeroy
na SPOBobnost' k polimeriZatBii Yinil'Inykh proiz~vodnykh tiofena)
PERIODICAL: Zhurnal fizicheskoy khimii, 1958, Vol. 32, Nr 8, pp. 1847-1850
(USSR)
ABSTRACT: According to.data in publications the derivatives mentioned
above are cap~tble of forming polymers having,dieleotrio pro-
perties simikar to those.of polystyrene and having a higher
softening temperature. An investigation of these compounds is
also interesting as the influence exerted by,the type of dif-
ferent substituted heterocycles in the ethylene'molecule may
be inybotigdted with re-elect to the polymerizability and the
properties of the compounds obtained. In 'he present paper the
number of oondensed benzene rings in the initial monomer was
inoreased, and therefore 2-vinyl thiophene and 2-Tinyl dibenzo
thiophens were synthesized. The polymerizability was investi-
gated according to the ailatometria method, viz., in the first
solution with 0,5 mole% of benzoyl peroxide (in block and
Card 1/2 solution)l and in the second in solution at B01 90 and 1000.

BOV/76-32-8-19/37
The Effect of the Monomer Structure on the Polymerizability,of Vinyl
Derivatives of Thiophene
The operation technique has already been described. It was
found that analogous to the furfurans series the introduction
of condensed aromatic rings into the ethylene molecule in-
creases the rate of polymerization. Besides the heat resistance
increased to more than the double and the dielectrio properties
also improved oft the occasion of the transition from 2-vinyl
thiophene to 2-vinyl dibenzo thiophens. A comparison of the
polymers obtained With than of the furane series shows' that the
latter exhitit wore& prop'ertiesi There are 5 figures and 10
references, 3 of which are Soviet.
ASSOCIATION: Akademiya nauk.WSR~Institut vysokomolekulyarnvkh soyedineniy
(AS USSR,Inbtitute of High-Molecular..Compounds)
SUBMITTED: March 21, 1957
Card 2/2

50)
ATITHORS: Andreyeva, I. V., Koton, M. M. SOV/62-59-3-28/37
TITLE: On the Polymerization of a-Methyl, Styrene in Solid (Frozen) State
(0 polimerizatsii a-metilstirola v tverdom (zamorozhennom)
sostoyanii)
PERIODICAL: Izvestiya Akademii nauk SSSR. Otdoleniyo khimioheskikh nauk,
1959, Hr 3, pp 552-553 (USSR)
ABSTRACT: This is a brief communication on the polymerization of styrene
in the block with gaseous 73 in solid state at -800 (freez-
ing point of styrene -230) in an atmosphere as dry and free
from oxygen as possible. Under the same conditions a-methyl
styrene was polymerized in a yield of 85 %. The polymer is
soluble in organic solvents (benzene, toluene, chloroform, etc)
and Is precipitated from methyl or ethyl alcohol. The data on
the polymerization kinetics of' -i-methyl styrene are given on
a figure. As may be seen from it, the pressure of gaseous BF 3
in a block (without cracks) exercises only an unimportant
influence on the polymerization of styrene. From the data
mentioned in the table it may be seen the the yield of poly-
mera, their molecular weight and the melting temperatures
Card 1/2 increase with the decrease of the polymerization temperature.

q
On.the Polymerization of a-Methyl Styrene in Solid SOV/62-59-3-28/37
(Frozen) State
There are 1 figure, 1 table, and 1 reference.
ASSOCIATION: Institut vysokomolekulyarnykh soyedineniy Akademii nauk SSSR
(Institute of High-molecular Compounds of the Academy of
Sciences, USSR)
SUBMITTED: July 18, 1958
Card 2/2

!Z_7
28650
S/020/61/139/006/017/022
B103/B101
AUTHORSi Koton, M. M., Corresponding Member AS USSR, Andreyeva, 99
Andreyev, P. P., and Rogozinaj E. M.
TITLEt Comnlexea of polyacrolein with heavy-metal salts
-3-,. -.. .
PERIODICALt Akademiya nauk SSSR. Doklady, v. 139, no. 6, 1961, 1372-1374
TEXTt It is noted that samples of polyacrolein powder obtained under
different conditions differ in their ability to form coordination complexes
with heavy-metal salts. The strongest ability to cause such reactions
has ura-,kyl nitrate. In the pH range investigated salts of Fb, Co, Mn, Cu,
N-4, and Fe are not able to form stable complexes with polyacrolein.
Conoerning the extraotion of heavy-metal salts with organic compounds, the
authors refer to papers by V. M. Vdov *enko (Xhimiya urana i transuranovykh
elementov (Chemistry of uranium and transuranic elements) Izd. AN SSSR,
1960) and V. 1. Kuznetsov (Usp. khim., 31, v. 6, 654 (1954)). The maximum
quan-.i+.y of uranlium (2305-10-6g/g) was extracted from aqueous solutions by
means of polyacrolein samples obtained by polymerization of acro.lein in
Card 1/3

28650
5/020/61/139/006/017/022
Complexes of polyacrolein with heavy-... B103/B101
aqueous solutions under the action of the redox system K 2S208+ AgNO3 which
is somewhat more effective than. the system K 2s 208+ Mohr's salt. Disacryl
and polyacrolein obtained under the action of K 2S208 + Na2 5203are less
effective. The poorest extracting agents are samples of polymers obtained
at low temperatures in the presence of boron trifluoriae or by means of
lithium butyl. The authors established a relationship between the content
of alda~qde groups which are able to form oximes and the ability to
extract uranium from aqueous solutions. Uraniur can be extracted in the
range of pH3 - PH4. Outside this range the percentage of extracted uranium
drops q,;ickly. The distribution coefficients for different samples of
polya,.rola~_n differ by a factor of ton (from 0-005025 to 0.04803).
Uranium absorbed by polyacrolein can be quantitatively dissolved by dilute
ECI. There are 2 figures, 2 tables, 4 Soviet ard 6 non-Soviet references.
The reference to English-language publication3 reads as follows: J. S.
A~iderson, Nature, jjA, No. 165 (1950)-
Cari 2/3

28650
S/020/61/139/006/017/022
Complex9a of polyacroloin with heavy-... B103/B101
ASSOCIATIONs Institut vysokomolskulyarnykli soyedineniy Akademii nauk '
SSSR (Institute of High-moleoular Compounds, Aoademy of 4
Soienoes USSR)
SUBMITTM April 81 1961
Card 3/3

ANDREYEV, P.F.; MDREYB.TAj,I,V.j ROWZINAt E.M.
Reaction of uranyl salts with the components of plant tissue and
some of its derivat'vea. GookhImlia no.4013-317 '62. (MIRA 160)
..(&an.vl salts) (Plant cells and tissues)

'1,
#_-
36292
sl19ol621004100410081019
B119/B136
AUTHORS: Andreeva, 1. V., Koton, 11. M., Kovalevaq K. A.
TITLE: Polymerization of acrolein and its derivatives. I. Low-
temperature polymerization of acrolein and a-methyl acrolein
PE11IODICAL: Vysokomolokulyarnyye soyodineniyap V- 4t no, 4, 1962, 526-532
TEXT: Acrolein (1) and a-methyl acrolein 0 (2) were polymerized in the
preuence of gasco*as BF3 between 0 and -60 C in block and in solution
(solvent: CH 2C1 2) . The experiments were made in sealed ampoules, partly
with exclusion of 02 and H 20, partly in the presence of very small amounts
of H2O-Results4 Polymers obtained in block polymerization with 10-15rlfo
conversion are completely soluble in organic solvents. With a higber
deGree of conversion, the reaction product becomes insoluble in organic
solvents but soluble in sulfurous acid. The reaction with 15-2MA
conversion without H20 takes 15-30 hr at -20 0C, with H20, 3-8 hr.
Card 1/3

s/igo/62/004/004/008/019
Polymerization of acrolein and its B119/B138
The molecular weight of thd polymer produced in the presence of H20 is
lower than in the one produced without water. Maximum conversion was
attained at -20 to -40 OC with 1.5 mole% BF (with 1) and 2.5 - 3 mole%
3
(with 2). The block polymers give no aldehyde reaction, they are cyclized:
CH CH CH
2 2\ 2\
7H VH CH CH Polymerization of acrolein in solution
CH 0 /CH 0 ICE 0 /,C
0
givon a soluble product*%vith a melting point of 150-170 C and
JI'l (,.06 - 0-07 in benzene at -600c and 301o conversion, but an insoluble
and nonmelting product at -200C and 30% conversion. The polymer obtained
from dilute colutions is not cyclized. At -200C the rate of polymerization
decreases in the order acrolein a-methtyl acrolein - a-ethyl acrolein.
There are 4-figures and 1-table.
Card 2/3

E
075/E436
AUTHORSt Andreyon., _I-V Andreyev P.F#, Rogozina, E.M.
TITLE: Investigation of the process -.d products of
interaction of high molecular weight compounds with
inorganic salts. I. The formation of polyacroleir.~.
complexes with urpnylnitrate
PERIODICAL ho.6, 1962,,66o-667
F Radiokhimiya, v
TEXT: The complex formiag ability of,various polyacroleins
was examined for the'first time. This work forms a start of a
long-tcem investigation of complex formation between metals and'
the derivatives of polyacrolein and other-polymers with carbonyl
groups. The polyacroleins investigated were obtained by
1) polymerization of acrolein in water in the presence of
oxidation-reductI.on initiators; 2) polymerization of pure, dry
acrolein without initiators; 3) low temperature (-200C)
polymerization in the presence of traces of H20 or BT
4) polymerization In benzene solution * Na; 5) bloc
polymerization in the presence of lithium butyl at 200C. The
complexes with U02(NO3)2 were formed in-aqueous solutional their..~'
Card 1/ 2

ANDREY(EVA, I.V., KOTON, M.M.; KOVALEVA,, K.A.
Polymerization of styrene derivatives in the solid (froxeA) Oute.
Izve AN SSSR.Otd,khimenauk no.lq:1890-1891 0 162. (NIRA 15:10)
11 Institut aokomolekulyarnykh soyedineniy AN SSSR.
(Styrenle (Polymerization)

ANDRSX3VA,, I.V.,- AMRMV) P.F.; -RWMINA) S.M.
Proaasswand.interaotton produets of macromolecular compo=ds
with,inorgazLic Part 2: Formation of corplexes of
poly(purmethyl)acr ein w-Ith uranyl nitrate. Radiokbimiia
5 no.1:103-106 163. (MIRA 16:2)
(Acroloin)
(Uranyk nitrate)
(Maeramoleoular compTaids)

S/020/62/144/005/013/017
B I 24/jB 138
op to
AUTHORS: Koton, IL M.; Correoponding Member, AS USSHf Androyeva, 1. V-j
and Getmanchuk~ Yu. P.
71TLE: Emulsion polymerization of a-methyl acrolein in the presence
of various redox systems
PERIODI.CAL: Akademiya -iauk SSSR. Doklady, v. 144, no. 5, 1962, 1091-1093
TEXT: a-methyl acrolein was polymerized in various redox systems in the
presence of a new type of emulsifier, aqueous polyacrolein sulfite. This
yields a stable emulsion, and polymerization takes place in the micelles of
'IV
the emulsifier. Polymerization is carried out in ten times the amount of V11,
water with audition of twice the amount of a 2 % aque-ous emulsifier, all
related to the monomer usuld. The most suitable redox system for thi's scope
is potassium persulfate and silver nitrate which gives high polymer yield6
of maximum molecular weight. All a-me,thyl-aoroloin polymers obtained
contain 65-70 ~ aldehydic groups, while for polyacrolein preppxed in the
same redox ssstems this figure is 20-70 %6 This ib due to the mothyl group
in the side chai.n ckf the a-methyl aorolein molecule, which pievents the
Card 1/2

KOTON"M.M.j ANDaEYLVA,,I.V.; ANDREM, P.Y.; DANILOV, L.G.; RDGOZINA, E.M.
Reaction4, 9f an aqueous solution of polyacrolein with inorganic
salts. Dnlkl,.AN SSSR 146 no.3:60f-61q, S 162. (KIRA 15:10)
I* Institut vyaokomolekulyaruykh soyedinsaiy AN SSSR,,-2,, Chlen-
korrespondent AN SWIM (for Koton).
(Acrolein) (salts) (Macromolecular compounds)

KOTON, M.M.;.~VDRE _-I,.V.; GEIMANCHUK, Yu.P.
Polvmerization of meta-acrolein with anion catalysta. Dokl. AN
SSSR 155 no. 4:836-838 Ap 164. (MIRA 1-1:5)
1. Institut vysokomolekulyarnykh soyedineniy AN MO. 2. Chlen-
korroupondent AN sssR (ror Koton).

ANDREYEVA 1.V,; AND."MIMN, P.F.j DANILOV, L.T., ROGOZINA, E.M.
Processes and proiucts of the in' raction of high-molecular
weight compounds with inorganic alts, Part 31 Reaction of
aqueous solutions of polyacrolei .. ladioklilmlin 6 no. Is
86-93 164. (WRA 17%6)

ACCESSION NR: AP4020057 SJOIU616410061001/0086/00h
AUTHOR: Andreyeva, 1. V.; Andreyev, P. F.'; Danilov, L. T.; Rogoz4na, E. M
TITLE: Processes and products of reaction ot high molecular compounds with
inorganic salts
SOURCE: RadiokhlmiyF-. v. 6. no. 1, 1964, 86-93
TOPIC TAGS: polyacrolein inorganic salt reaction, polyacrolein reaction,
polyvinylalcohol, coagulation, gel formation, metalprecipitation, variable val-
ence metal reduction, polyaldehyde, hydrated aldehyde group, t:horium polyacro-
lein complex
ABSTRACT: In continuation of earlier work L polyacrolein and its ability to ex-
tract metals from aqueous solutions, a number oi reactions were run or attempt-
ed between 3% polyacrolein and 3% mineral salt solutions. Aqueous solutions of
polyacrolein have a series of characteristic properties explained by tne presence
of an external hydrate shell and hydrated aldeny'de groups for the polymeric mol-
eculq:
ard 1

ACCESSION NR: AP4020057
acid medium. The complexes formed have constant compositions, differing
depending on pH of the media. In acid solution one thorium atom is complexed
with 24 or 28 elementary ligand links; at pH 4. 73 and 8. 32, with 8 and 9 linicages
regardless of the ratio of the reactants. Reaction with potassium bicnromate
and ammoniacal solution of hydrated copper oxide gives, as do polyvinylalcohol
solutions, galn which are insoluble in water. The structure of the polyacrolein-
hydrated copper oxide complex may be represented by geiation of polyvinylalco-
hol. Preliminary data obtained indicates that elements with variable valence
can be reduced with aqueous polyacrolein solutions under determined conditions.
It is therefore assumed that the polyacrolein molecule can react as a polyalde-
hyde. This capacity of polyacrolein for many chemical and physical- chemical
conversions makes it a theoretically and practically interesting material. Orig.
art. has: 4 tables, 7 formulas, wd 1 figure.
ASSOCIATION: None
SUBbUTTED: Mept12 DATE ACQ: 31MarG4 ENCL: 00
SUE CODE: VTj GG NO REF SOV: 003 OTHER: 005
Cord3/3

L 16o88_6c;_,. E;W.T(m)/EPF(0~jV_zP
-CCE 8 S I ON -Of-7 AM 91 3-.- ":V6020/64/
159 /003/0602, egIM51i
XI~TrOlgpon
--uw-_ 77~
'i k-il
V
_Yav G
TITLE t f h ketone
polynerizatt o- giroxy2henyl vinyl
SOURCE: A9 SSSR. Dokl,adyh, v, 159, no. 3, 1964, 602-604
..TOPIC TAGSt chel-ate polymer, o-hydroky.phenyl vinyl ketone, polymer,
1 metal chelats copolymex,, Methyl methacrylats, divinylbenttne:
B - S T RA ZT i ; T h 7 i n--d -t _16 at4on d
t vme
-tu'dfed-_rh_7_i__1e_ -o-r t ~_qob_tain ---- po-:Ly-~
tViny'l- etone~ rige-r-5---c-on
ny 9
t'--" i it at on or cop
-0 lyme ri 2-4 t-i
,on
T 7 _~f ___ -, - -1 - .
t -'a ze specidlly-16r th ---
+ he o_-hydrbxyph0_tiy1--viq1-' i 1 oi'n e'- 9 Q e 'study'
was'polymerized in-,a* nitrogen atocaphere by su'veral methodst i
. - 11 R - . .. I-
6 _bu~lk, ind i il :9 : -'-- '.
on -do
Goluti Ln
f
a I'ators if PbLymer a tion.
Cz
V -1 ------- 75'- 8.M 'col-orle6s-, (af ter reprecipitaki )'..powde
-amp a ra ure~was T a
like polymer Is

L 16088-65
ACCESSION NRt A?4049923
acetonei, pyridiue,,-or--diuethylformemides and in dilute alkalis: it
insoluble In methanol, carbon tetrachloride, or ethyl ether. The
imolecular weight of 125,000 vas-determined by the light-dispersion
!method. The intrinsic viscosity of polymers depends on the method of
lobtaining them. The lovest-Wes were obtained for the product
1polymerized In solution; the bIgheatp Ir suspension. The kinetics of;
ithe polymerization were studied, and the curves and the constants
~wara obtained. The IR -spectra- confirm that polymerization takes placi
7 only along the double bonds-* -The a2ime derivatives confirm the pre-
~sence of the theoretical number of carbonyl groups in the polymars
.obtained. Products of q2yolymsrizationqof o-hydroxyphenyl vinyl - -
:ketone with methyl methaery.ate (br dMi4ylbenxene were also obtelned;t
_properties~. The presence-of
the latter Product hWs-Ion_s-z0h4#ge
ps -in the polymer# studiod makes it possible to us
chelate grint these
p____, piers' or--copolymers-1 or __o4t*.InInj_.;polymeric, -complexes --with -talss],~
oly :e
i
e4R.17 an
9
ASSOCI a 'k
AfIONJ~ i-.':IUiBtitUt~vy,*46kasolak'Ul~1 rny hsoyeeineniy'AkadevfW~nauk
(In' titut --of -Mactolviidlelii~ulalr--Co c an
C
a vapounds Academy-of 6 1
-SOS ------- - -
Card 2/3~

.U'kVlN, V.K.; AYMYLVA, I.V.
I
------
Inactivation of the phage genome A by acridine dyes following
infection with Fscherichia coli K12S. l4ikrobiologiia 33 no-5:
819-823 S-0 164. (lqiRA 18:3)
1. Institut biofiziki AN SSSR.

ANDREYEVA, I.V.j RGGOZINA, E.M.; ANDRMV, P.P.
'Processes and products of the rpection U high-mole-cular coiffpounds
idth Ifigrg'anib aalts.-Part 5t rhysicochemical studies of the
reaction'bf pol~acrolein with inorganic salts. RndiokhiTniis 7
no 01:83-90 163. (MIRA 18:6)

RAVI 11, V.K. -. J~ i% P! &: Yl-, VA , I.V.
Effect of ultraviolet irradiation on the temperate phage-tecteritm
complex In various stages after its formation. 14.1krobiologlia 34
iic-~.IMC-113 Ja-F 165. (MIRA 18:7)
1. Inotitut biologicheskoy fiziki AN SSSR i Institut mikrobiologii
i epidemiologii Imeni N.F. Gamalei AMN SSSF.

GFRSHANOVIC-3,11, V.N.; BURD, G.I.; _MOTLEYEVA, I.V,; .njD,,V, V.A.
Effect of phagm T2 "ghosta* on the synthesis of inducible beta-
galactoBidase in Eacherichin coli B calla. Bickhimiia 30 no.2:
395-406 Mr-Ap 165. (MRA 18:7)
1. Institut, epidemialogii i mikroblologii imed Gamalai AMN SSSR,
Moskva.

ANDREYFVA,, I.V.; XESHV*.%'AN, G.O.; ANDRRYEV, P.F.; DANILOV, L.T.
Processes hi.1 products of the reaction of macromolecular com-
pounds with inorganic salts. Part 4t Reaction-of aqueous solu-
tions of polyacrolain with tannin and gelatin in salt solutions.
Radiokhimiia 6 no.4t491-493 164. (MIRA 18:4)

ACC NRAP6034385 SOURCE -COI)9;.--W/0-4W/66-/000-/005/0~r)T3/057
AUTHOR: Ravin, V.
ORO: Institute or B4ophysicap AN SSSR (Institute bioloricheakoy fiziki
AN MR); Institute of EpidemioLogy and microbiology im. N. F. Gamaleir
AmN,SSSR, Moscow (Institut epidemiologii i mikrobiologii AMN SSSR)
TITLE: A mutant or x bacteriophage resiztant to acridine-orange
SOURCE: Voprosy virusologii, no.. 5. 19660 575-578
TOPIC TAGS: virology, cytology, immunology, ~bacteriop~age, DIV)
ABSTRACT: A mutant of A bacteriophage resistant to acridine orange
both vithiq and outside the cell was obtained from cultures
of 96 coZi K 12k. The mutant was sorologically identical
to wild-type phage, No differences were noted between
strains in lysogenic capacitys sensitivity to ultraviolet
UDC:576.856.9-695-57-097.22:615-778.292

AUTHORS: Yefremov, G.V., Andreycva, I.Yu. 54-10-2-12/16
TITIE: The Co-Precipitaticn of Thallium and Cadmium Sulfide
fSoosazhdeniye talliya s sul'fidom kadmiya)
PMT-ODICAL: Vestnik Leningradskogo Universiteta,Seriya fiziki i
khimii , 1958, Vol.1 0 , Nr 2 , PP- 117-121 (USSR)
ABSTRACT: I.P. Alimarin (Ref 1) and other authors showed that cadmium sul-
fide is a good collector for microgram quantities of thallium. In
view of the quantities of thalliwn that are usually lost in pro-
duotion and because of the difference in the conditions of co-
precipitation, the authors studied the oo-precipitation of thal-
lium with cadmium sulfide. Final determination vas carried out ac-
cording to the calorimetric method by the application of methyl
violet after oxidation of the thallium by bromine,water. Under
prevailing conditions the 10nslOmr? and dcl~ are formed, which,
according to data' supplied by II.T.Voskrese kaya (Ref 4) form com-
4
pounds with vat dyes mid thereby render the determination of thal-
lium difficult. It was found by an investigation of this develop-
ment that if UP to 75 milligram of cadmium are present, the in-
Card 1/2 fluenoe exercised b-r the ion [OdBr,)" is so small that it is hardly

The Co-Precipitation of TIkillium and Cadiaium Sulfide 54-10-2-12116
manifested at all in results obtained, nor vas thallium determina-
tion i-nfluqnced in any Ymy by the presence of the ion [CdCl 7 " un-
der the same conditions. Average values of the precipitatD per-
centage of thallium for different correlations of thallium., cadmi-
um, and pH solution are given (table 1). It may be seen from this
table that the highest co-precipitation percentage is found at
PH 5-5,6. Both an increase and a reduction of pH, conditions other-
wise remining the same, leads to a reduction of the percentage.
Precipitation of sulfide vas, in the case of all previous experi-
ments, carried out at a temperature of 70-800. At lower tempera-
tures precipitation is finely dispersed, and therefore co-precipi-
tation of thallium increases. At low precipitation temperatures
(200) the coagulation of the precipitation is made difficult. For
a long time it remains in the form of sol (table 3)- In the case
of repeated precipitation of cadmium. sulfide thallium can practi-
cally be fully eliminated. The values obtained show that the co-
precipitation of thallium Yrith cadmium sulfide takes place mainly
at the expense of surface adsorption. There are 7 tables, and 4
referenoes,&U of which are Soviet.
SUBMITTED: December 25, 1957
AVAIIABLE: Library of Congress
Card 2/2 1. Thallium-Precipitation 2. Cadmium sulfide-Precipitation
3. Thallium-Datermination 4. Cadmium sulfide-Determination
5. Colorimetry-Applications

YM2WOTV
Copmol itation of thallium with cadmium'sulfide [with suzmaz7 in
3tagimb Vast. IGU 13 no,lOtll7-121 158, (MIR& 11W
(Thallium)
(Cadmium sulfide)-

S/032/601/026/012/012/036
B020/BO56
AUTHORS: Fraiki`nj Z. G. and Andr
.TITM The Spectroscopic Analysis of Impurities in High-purity
Sulfur
PERIODICAL: Zavodskaya laboratoriya# 1960, Vol. 26, xo,. 12,
pp. 1370-1371
TEXT: Two methods of determining the purity of high-purity sulfur by means
of spectrum analysis were worked out, namely the direct spectroscopic de-
termination and the determination with previous enrichment of the sampke.
Work in this field was carried out by A. N. Bronshteyn and L. M. Ivantsov
(Refv-1). In the oassi of the first me'thod, the standards were prepared in
such- a- manner that the e,',,eme,nts Fe, Co, Cu', Ag to be determined were mixed,
is sxklfid9i,Aog9ther with sulfur into a jasper- or agate mortar, and alu-
.%4um was introduced as Al 20 30 The spectra were recorded by means of the
,speotrograph WCn-28 (ISP-28). Aa exciter, an a.c. aro with an amperage of
7*k was used. The sample was pressed into the channel of the lower carbon
electrode, whose diameter was 3 mm and whose depth was 4 mm. The upper
Card 1/4