SCIENTIFIC ABSTRACT ZHURAVLEVA, I.T. - ZHURAVLEVA, M.G.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R002065020018-7
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: July 16, 2001
• Sequence Number: 18
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT


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ACC NRt AR6010585 SOURCE CODSt UR/0081~6 000/018/SOlq/ 19
AUTHORs Rode V. V.; Zhuravlova, I. V.1 ~2,flkovo S. R.
TITLE: Th rmo dat16n of phonolphtalein-based.polyaryl so.
'SOURGEs Ref zh. Kbimiyal Aboo 18SI16
~REF SOURCE i Vestn. tekhn** i eko*n.,inform. N.-i. in-4 tekiini-ok0i. In led; ;Goo
kom
-ta khim. prom-sti pri Gooplane SSSA, vko 120 1964t X~-14
TOPIG TAGSs thermal decompositionj ox1dation kinaticz, oflyeatbr, plastic
ABSTRACT.- The process of thermooxidative destruction of'heteiro(ihain phenol~ht&iein
.2- polyesters, isophtalic '(1) and,terephtalic acids (2) at toppexaflures of 3500 to 5000
on air and in a closed system under static conditions at: an O,Z pressure of 120M H g
c0lumn) is studied by the continuous weighing method. Kinetie ~uxvets for (1) and
(2) weight loss were plotted. The rate of destruction exPoneatially depends on ths
temperature and in presented by an equation of t1Ae first-orrdei*.~ The offective
activation energy of destruction for
(1) and (2),is equal 29.2 11 31.5 kkal/mol,,
respectively. The study of the thermal destruction or (2),in woclostxi systm ohowed
that the sole gaseous products am CO and Go. The thermal dostruction ot J2.)
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International symposium oil macromolacular chestistry. Moscow.
196-0.
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,Chemistry Held in Moscow, June 14-18, 1960; Papers and
3&U
19601
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Sum=&X'l*,al,Soatlon 111. EKOscow. Xzd-va AN
V. 000 copies printed'.
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Sponsoring Ageacyt The Internstj ... I union of Pure and Applied
Chemistry. CO=m15aIOM an Kaormal.c.l.r Chemistry,

rL=WZ% This book Is latend6d for chemists Interested In poly-
werlagtion reactions =4 the synthesis of high molecular
--comocunde
COTMU=3 We to 3ootion XU Of A SALItIT0110 work contain-
Lae papers an m=rocLol0cul&r chemistry. The articles In
general deal with the bdn*tlcs or polyme.-Iz&tion rm&atI,,,s,
M4, 6"theals Of specIal-parposet polymars, e.g., Ion ex-
Change resins. semiconductor materials, eta.. methods or gat-
&4zlna Polym9rizatian reactions, properties and chemical
interactions of high molecular materials. and the, effects or
various factors an Vo1"*rIzxtIv= a=d the degradation or ..
lar compounds. ft personalities are vi&otloned.
a given follow the &rU*I*s.

1
and R. S. (WSR).
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On Method of Copolymer1:14 A
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Polystyrene and ParchlorovInyl-
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lcohol Under the Action or Zftys 207
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Lazar X, 7~ R d ' .14 (Czacaoslovajda).

Grartfus j6W1
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r7late Onto talyyropylene and Pa
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3tg -Rubbers.amd.-Ir nxtureff ;;Itft
=0 IAction or Gammal Radiation 293
V. A. DerevItsk Sun T'ang, Chang Wei-
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1(10) CZECH/3-59-12-9/39
AUTHOR: Zhuravl6vaj Ludya and N6me6ekj1,:Vec1av
TITLE: Soviet Helicopters

PERIODICAL:
KM'd1a Vlasti, 1959, lir 12, p 6 a'nd- lower par ~of~
t
p 7 (CSR)
ABSTRACT: Primarely this article lists types and design6is
of helicopters now in service in~,USSR. 1) KA~-101
2
KA-15 and KA-18 designed by N.I.Kamov; 2) Mi-1
(3 seater), Mi-3 (medical evacuation), M-4 (10-'12'
seats), Mi_6(50 seats) designed by 14~'L.Mill

y A* S..: Yakovl
3) Yak-24 and Yak 100 designed 1~ . I
ev. The
author points out that the phot6~'or any technical'
details were never released outside the USSR,~thus
making 1101'dla Vlastill the first
foreign.publidation
.
to carry any coverage on it. The d.evelopmenfoif jet-
propelled helicopters is the work of S-barichin.,
Zherebtsov and Breginskiy. There are 7 photos..
Card 1/1

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ZUBOV, M.F.; FEDOSEYENKO, LO-G.; SANIN, M.A.; PIVOVAROVA,I'T.K.;: ZILIBMINTS,;
I.V., kand. biolog. nauk; FADEYEIV.. Yu.N., kand, s,alOskokhoz. na4k;
aVLFVFA . L.M.; KIPIANI, A.A. aspirant; MLILINII(OV,: N.N.;
ZHU&L I
Ri- -I '.-VO P.; SHVETSOVA-SHIL&HAYA, K.D.; SHATOV oil,
0 ~LOVO G.K
SPIRINA, T.A,; SEDYKH, A.S.; ZINCRENNO, V.A.p aspirantka
From experiments i n the use of new preparations. Ushch. raat.~
0t vred. i.boL8 no.10324-216 0 163. JMA l7t6)l
1. Vseooyuznyy nauchno-iseledovatellskiy.ins.titut k1difticheskilih!
sredstv zashchity raotenly (foriZubov, Fedos6~enk.DiSanin
Pivovarova). 2. Gruzinskiy institut sashchity re-9tbniy:(f'or
Kipiani)~ 3. Moskovskaya ordena Lenina sellskolchoz y*aystvennay&
akademiya im Timirvazeva (for Zincheako).
q j

millillicMIMILRUNU -

S/07~~/6-f/9~1/002/014/019
B118/2208:
AUTHORS: Xirsanov- A. Vand Zhuiavlevat Lo- P.
TITLE: H-dichloro-phosphinyl carbamicaoid
PERIODICAL: Zhurnal obshohey,-khimii v 41~ 31 1n 2: '.1,961 59,a-604
Oo
TEXT:.' It,wasmto be, expected-from:Ret.. 11 that'.X-d chlor p oaphinylid'arbimic
acid formed by,treating the dichldride 6f,iaocyanat~-~ph^sp4orio'acid~with
water splits off readily C02 being converted to phoaphaxic,:scid,.dichloride.
Experiments disclosed that ieooyariatoo-phosphotic acid:,diohloride readily~
splits Off C02 with excess water, in:which connectioiip howevers,the,adid':
chloride part of the molecule is hydrolyzed
01 PONCO + 4H 0 30CO 4g=1 + NE H PO Addition of4aiter only'to.the
2 2
2, 4 2 4',
isocyanate:group, without:hydrolyeis ofsthe chlorinel4tcme' bound to'phos#=4
was possible.only by'the method of R. Graf:(Ref. 2)pJ.(1,41~ with conoentr Iated
hydrochloric acid. In this:way the dichloride of ispoyenato -phosphorid
acid. gives the thermostable N-dichloro-phosphinyl carbamic acid (I),.'
Card 1/3

3/079/%1 /031/002/01
./019
N-dichloro-phosphinyl ... BI I e~k:!oe
+H 0
2
ru 'con
Cl2PONCO ip, C12PONECOOH jts st oture was hrmed' by analyticali data
and the following reactions:. 1) Complete hydrolys is: givei HCl, NH 1 ico
x 9: 29
and
and H PO 2) reaction with PCl 'gives HCI, Pool CILPONCOI 3)~ trialkyl.
3 41
phosphates are formed~nearly quantitatively withalcoholej 4) with aniline,
the aniline saltof N-dianilidophosphonyl carbamic acid 10 U;lts 5Yheating
to 1600C gives HU) C1 PONCOt and:the polymer [HOP N OOHI Th. el. n1ilikie
0
2
salt of N-dianilidophosphinyl carbamic acid obtained';Ifrc,m'N-dichloro'~pho's-
phinyl carbamic acid and aniline hydrolyzes,when treated. with alkali!lye, to
give the sodium salt of dianilidophosphoric acid, anilii-.ei soda, and'NH
When heating N-dichloro-phosphinyl carbamicacid, the fc-Ilowing proctash
take place successively:
100
201 POINHCOOH 1600 >101. PONCO + 1 Oro+ NCOOR) -(HOPOHWx-
2 2 x x
(PO X6
x
Ldard 2/3,

'ACC'N1tf` "_AF1UUUb7Y'_
AUTHOR'. Ihuravlevap. V.
Z'
ORG: All-Union Scientific Research Institute of Railroad rr~n6port esoyuznyy
(Va
nauchno-isaledovatellskiy in'stitut shelez'nodorozhnogo kirans poita)
TITLE: Investigation of the corrosion resistance of aluminum alloys in a calcium
olution
chloride a
SOURCE. Kholodil,naya tekhnika, no. 11,~ 1966, 11-15
TOPIC TAGS, AMts alloy, aluminum magnesium alloy, manganes~,containingialloy,.
silicon containing alloy, refriger~ation equipment, 13TUY corrosibn.realistancef
AMg2 alloy, alloy, AMg5V alloy j AMg6 alloy t AMt al'Lo
ABSTRACT: Hot-rolled flat specimL-ns and work-strained~;tul:,ular,specimens,of~wrought
AMg2 (1.8-2.8% Mg), AMg3 (3.2-3.8Z Mg), Amg5V (4.8-~-5.51, lfg), AMg6 (5,~8-6.8% mg),
AMts (1.0-1.6% Mn) and AV (0.45-0.9% Mg, 0.5-1.2% Si) nl~mlnum alloys'were tested
for corrosion in a 30% CaC12 solution for up to 1200.111 at room temperaturei In
short-term tests up to about 178 hr, the corrosion rate ol of1the Al-Mg
the alloys
system (0-6.5% Mg) was significantly.higher in alloyalwithia higher magnesium con
tentf but it became practically the same in all alloyd'.vif:Wincreasing exposure
time up to 700 hr or more. The weight loss, of annealed Alfj2k~ Alfg3M, and Mg5M
alloys reached 2.1-2.2 g/m2. after a 100-200 hr exposure and,thcn remained practically;
constant# regardless.of the duration otexposure, The WeLg~t loss of~the alloys in
Card . 1/2'. UDC: 62N19:669,018-

ACC NRt AP7000675
ighei and-ine. eas.di.coatLnuously with In: reasing
he a emiwork-a trained condition was'h r
exposure time. Corrosion.tests of.pipes~with aluminum-~'clad inner walls' showed that
~,cladding with,aluminum did not improve~-the corrosion resistiincwof any investigated
alloy, except AMg5V alloy. Similar results,were also obtained in tests in flowing
corrosive solution. In general,:pipes made from the tested aluminum alloys had a
satisfactory corrosion resistance. Parts and piping fort~refripratlon cars and
installations Are best made from AVM and AMg5V alloyaj.'wkch arei~.readilyIhibrkated
rate of 0.037 and'O.035 mm per,ia
and have a low corrosion arAp flowing CaC17-solu-..
ion, respectively, Welded joints of these.'alloys also~hdve alsatisfactor~~Eorrosion
t
lea
resistance. orig. art, has I_2 figures and 2 tab
ORIO REFI.,00
SUN4CODSt ll/. SUBM DATRI.
S/ 6TH W1
J~,
-2/2
LCO.,

I 1WRIINLIMIM
S/0 9~1/60/630/607/02411'039/XX
BOO1/BO66
AUTHORSs Zalesekaya, T& Ye.:and Zhuravl4va:, L. 1e.
TITLE& Identification of Alky 1 'BI an zene S.1 I. mina Ly~si aof ~BinaIry
Mixtures of Acylamino Derivatives of.2-Phanil Butaneland
3-Phenyl Pentane
50~
PERIODICAL: Zhurnal obshchey khimii,.:1960, Vol. 59~' 6; 1) ppe 2164-21:66
TEXTs The purpose of the present work,'was:to iden,ttfy closely related
hydrocarbons that are constituents of a, mixture. lh,tordeti to identify
2-phenyl butane mixed with 3-phenyl pentanep the tw:6 hydiocarbons were
synthesized and converted to their acylamino derivativ. The thermal
analysis of the binary mixtures of the correspond in~: derivatives was made
under conditions applicable with small quantities of the~produotsltb bei
studied. The melting points of mirtureis of the benzalne derivatives' of
2-(p-aminapheny-1) butane and 3-(p-aminophenyl) pentane, rind of mixtures
of the acetyl and benzoyl derivatives of 2-(2,4-dI6~in phanyl.) bu ahe
and 3-(2,4-diaminophonyl) pentane were' determihed*Ixparlmental data
(melting points) are given in the following diagramst Diagram Ij meltiAg
Card 1/2

_~~Mj Jill WHAH" III
- - - - - - - - - - - -
Identification of Alkyl Denzeness 110 Analysis S/079/,60/0~0/007/02VO39/xx
of Binary Mixtures of Acylamino Derivatives BOOI/~066
.-of 2-Phenyl Butane and 3-Phenyl Pentans;
points, of the binary mixture, ~oftha. p-bekizoyl-amino dirivati-Vies of~
2-phenyl butane and 3-pbenyl pentane; diagram 2s:melting points of t1i
binary mixture -of the 294-di iscetyl'-amino'~ derivati.yee, of 2-ph6inyl but4'u*'e.
and 3-phonyl pentane,, diagram 3$ melting:points of tWbln~ry mixtur*~~Iof
the 2,4-dibenzoyl-amino.derivatives of 2-phenyl blatan6. and,'3--;pheny1'
pentane,'Under the experiment al conditions, not only the temperatures
measured when the solid phase disappears but also the, temperature during7.
the,appearance of the.liquid state is important for chkraiiterizing each
of the mixtures, as is clearly seen from the melting-poin-1; diagrams#
There are 3 figures and 4 referencest 1,81ovietp 2 US 9' and 1 Goormane
ASSOCIATIONA Leningr.adakiy.tekhnologiche6kiy- ins titutj-~sellyulozno-
bumazhnoy promyshlennosti (Leningrad Institut6 of
Technology for the Cellulose, and Cotton jndu.jt;rj)
SUBMITTEDs June 23P 1959
-Card 2/2

ZHURAVLEVA, L.Ye.; DANILOVA, Te.K. (Leningrad)
Underpround:gasification of coal, Xhim, y ekkole J.) ~na.10-5
JA-F 158- (MIRA 1102 12)
(Underground coal.gasification

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