SCIENTIFIC ABSTRACT YEROKHINA, L.I. - YERONIN, V.A.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001962830004-8
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: April 3, 2001
• Sequence Number: 4
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

1TIODUY L.A.; YEROK"IfIVA, i~.Al .
wo
Nachine sot fcr r,:-_; j"1
3,lodbeds. ~iul. teb-h.-ekon. Gns.
Ilauch. i tekh. inform. 17
0m. -YT..ll)

1GI.aMSFEU,t, V.O.j MAXOVFTSKIIJP K.L.; YEROXHINA, L,L,
Cyclic trimerization of acotylems. Zlnw.ob.kbjn- 32 no.2:653 -
F 162 * (KMA 15#2)
1. Laningradakiy tekbnolefficheakiy JaStitUt limmi jamsoveta.
(Acetylene)

MAKOMSKlY, K. L.; REYMSFELID, V. 0.,- Yll,'HOUINti, L.L.
siml-taneous cycUc trimerization of butylacsry~mfte h
phanylacetylene. Zhur, ob. Rhim. 34 no,6sl968-197C) Jis 164.
OLCRA 17:7)
1. Le-iingrAiy tekhnologictieskiy inatitut imenA Lennioveta.

,yJaOgBM L-39,- UARWOVAw C.S.; IATWHKINI M.P..$ otv6t-0ve=yy radaktor;
tokbdchookly red4iftOr
(Strest directory of Moscow; an of November 1, 19561 Npravochnik
ulits u0skly. Posostoianila ik's' I nollabria 1956 *9.~Oostd; L.S.
BrakhUm I 1.6.0srUsovs. Otv*torqd. CK4kYa. Isd-vo
axo4coveldi rabachits? 1956. 494 p. :(KUU 10:1)
"atora
(Moscow-streetl)

OVCHUMOU V.7,; BRMMOUp M,N, I YAMMDIYMp S,-Ih,
KOP*f at** redol DUMVAP I%# Mel blMOVAO A.t
[streeu of Gteater Moscow; a tuid#. As of Fstruary 101 1961.,
ul-itsy Bol'shol woetoianiiu na ~ 10 for-
Nook*y; -i**vocbiL%. PO ~
ral4m 1961 g. Moskvit Xosks rabooblip 1961. 551 p, (NBA IA,t6)
1* Mookc ~vkoqz kontom
(moscov-strests)

SHURINOVAO M.N.; LAVOCHKnj~p m.p*p Qtvq riPdo;
SULTAKOVAp N.p red.; TAKGVLEVA, Xw*p tekbn.redt,,
[The streets of Moscov; a inamial ~as of Septembe'~r 1, 19631
Ulitsy Moskvy; spravocbnik po,sostoianiiu na 1:sontiabria
1963.g. Moskva,, Mosk. rabochiij, 1964,,, 477
~4k 17:3)

vr-jj0'tjr JN#9 4 - V
ArmMOT, A.1h., Icind.bi6l.naukg, DA2=0' A 03's 1, kand'. it~V skoldws.tauk:
BRMISMA, K.A.g bW.tGkhn4=i Gown K.Ato, kand.obiolog.
uaukj~ GORD(No reek4t kandoeimtkoami*t DmWKWvv* IN.,-irlbowdp-blolog;
I
r, :HUA, L9T., rybovad-btolog; MOIN, T.M." 31bmli-blolog;
--mm' -
I 1T1;-X.-r.-.rybovo4-bLo1cgt UPOMON, 0.1,4 lrybovI341-biolog;
KOKA110TA, I.V. 9 kand.blol.'nauk; MIM)WA R.T ~ Jrftavildf-molog;
4'
KULAIUVA, A.M., ryb6vod-biolog; Fft~h' L:k j,' kand,biol,nau1c;
KUSIAR, To.V,. ksnd,bio1.aauk-. kILUM, P.T.0 Azn&#~ibl.maukt
XMUINA, R.I., kand.biola3j&ukg PAZHGIWO SmP,0~1and,biol.namk;
Sm"Um". F.M.. ksnd.b1ol.nstLk.- SUOWYA, X.P.. i7bcyvod-bio-
log; TSIUNCHIK. R.I.* ryboyad-biolog-, RTZHMj K,I,,t red*; KOSOVAt
O,U,,, red.; SUOLCTA, L.Aop tokbhorsda
ERandbook ork pond fish oultural OprsivoaWkp~ prud~ovomu rybovodetyu.
Red.frollegiial A.I.Isaev I dr. Koekva, FlohAii1iromisdat, 11959. 374 P.
(KM 3,3:4)
1. Wacow. Yearossiyakly nanahna-le Ialedovate1jaklyAnatitut prmdo-
vodo rybnogo khosymystvae
Illah cultun)

VLASMV# B.V.; YEROXHINA, L.V.
Increase of the reproduction capacity of comeraw zonusks (unio
species) with reference to the reproduction of ralir material
of mother-of-pearl in our inland waters. Report 11o. 1. Problems
and methods of work. Trudy Gidrobiol. ob-va ll.%,')q4-1P05 961.
(MIRA 15:1)
1. Kafedra. zoologii bespozvonochnykh Moskovskogo, Igosudarstvennogo
universiteta i Vserossiyskly nauchno-issledovatel4skiy institut
prudovogo rybnogo khozynystva, Moskva.
(Unionidae)

~,.'Tll, F -T
---.L 101W~: M62
M.46 Mt XK;)Vd4e:)O livuhurf i WIM: ulibel
L. V.
AUVIOR: Yerokhi at
omi rnstitute of Ctnetics, Academy of' Saiences!
ssn (rnAitj
nault
TITIM Study of the change In the pratueolytic Mtlvity of whi
exposed to total-body x-ray irradiation
/M
SOURCE: AN SSSR. Itistitut genetiki. rudy., moh ;39.~ 10~ I
T
chilth lzlucheniy na vastLtelInyy I zhivotayy erg~niznw (Eirfeci
on plant and animal cirganisms), 253-256
TOPIC TAGS: animall physiology, blood, biologic *tabolism, r'
proteolysis, =use, 1-yrosine
ABSTRACT: A study was conducted of changes In the pro.teollytil
of totally irradiateC animals at differeni perio" atter irra~
2.5 months old were gubjected. to 600 red of, iv~i with oi~ dosi
Blood samples were to-ken from expertmenW., ind cOO'tv*1:anj=ij
21 days after irradiction. Experiments shovedt rrsd1aW
dnaa PosimaA an 4novamaga 4n fliss tv"et4nis mnrL*.ak*'wr trlhr%la hInru
:f
j&ew4uia, Akaditmlya
i~ bloWl In mice
stvl tal lonizir%Wus
, h-~
r ioi:Lzing radintioTI
atioit biologic offeat,
:tiv~lty in vhole blood
tiomi. tKice 2 to
Dve,~. aIf50 radjoln.
2 1141 T 14, 6nd
I ~ , ~'O , 91
~~r m.4je 'with this
-%v- +~Ign Onfirp

radiation (Bee Fig. ji.). -It was fount, hat the. i UAM imity pf VFT'~ 114.15 in the b.loud
1/3
Iu!
IT

i Ito
lid ix
I -Its_
C
Days after irradiettion Daye elt6i !irroilAtion
Fig. 1. T~Toslne content in the whole Wool
Fig. 2. Adij ~pi~bteint.64,
blood of irradiated mice activity,.'
I - Experimental mice; 2 can- Rrpetime .~L ml~qi; con-
trol ndce.
trol mIc4.
an antiprot.eolytic
-factor-In normal blood vItich ita*lases!~ sha 1~liq My 14vthe
blml. of irradiated animals, and thus Is the win, mul O~lg eA
4 4
has: 3 figures and 2 tables.
(J[31
2. ~.i
Cmd
~111L,411i~

VINOGRADOV., L V
Iffeativeness of feeding carp with grwmUtedi~06d.,1rud7
ov. Ikht. kam6 xW.14:53~-58 16243 (MnA 15: 12)
Vearosoiyaldy nauchno-Loiladavitallski7 inAl.tut'prudavcgo
"dgo khozyaystva (TEPRKh).
-i,,Oarp)
(Fin beg-Food)

BRUMP SON.; URRKHINAt M.V.
Roie- of the temperatitre and Our's oultures of UcUc, gicid bacteria
in the production iovsUpn of WauerkrauteMpicklao. Kons.
and prow
i ov.prom. 19 no.1:22-24 Ja .164'. OGRA l7s2)
1. Moskovskiy institut narodnogo khozyVetva Imni M.Plakhanava.

67302
0
AUTHORS: Galavanov, V. V., Yerokhinap X. A.
TITLEt Production of a Valve Photocel1Tof In3b With Fu~ed n--p unctionlk
PERIODICALt Fizika tverdogo tela, 1959, Vol 1, Nr 8, pp 1198-1200 (U:ISR)
ABSTRACT: First, reference is made to several previou's papers. Investi-
gation was carried out on monocrystalline n-type InSb with an
impurity concentration of 1013 to 1017 cm-3. For the first time
cadmium was used as alloy metal. A conductivity type inversion
is possible also in fusing indium to n-type InSb. This fusing
is brougth about in graphite containers In wa ar~gon atmosphere
or in vacuo (10-4 to 10-5 torr). After fuiion tho existence of
thep-n-junction was concluded from the sign of the thermo-
electromotive force. The fused junction of Cd with InSb had a
hole-type conductivity. In indium a p-typo conductivity was ob-
served at the boun6ry between n-type InSb crystal and In-In3b
alloy. The electric contacts were made by 301dering the elec-
trodes to the alloy of InSb with Cd (or In) and to an InSb
crystal with tin. Tungsten rubbing contacts iNere also used. The
Caxd 1/3 elements thus prepared were illuminated by,intermittent light

67302
$OV/161-1 -8-7/32
Production of a Valve Photocell of InSb With Fused n-y J~Actioin
from a projector lamp (340 w) or from a millit resistor heated
up to 10000. The light beam fell upon the photocell on the side
of the InSb-Cd (or In) alloy or also from the opposite side.
In toth cases the alloy of InSb with Cd (or in),becaime charged
positively. The variable signal coming fro~,the-photocell was
the transmitted to a broad-band amplifier of th4 28-IM type.
The photooells thus produced have a considerable light aensi-
tivity. The photo-e 'lectromotive force depends on crystal aur-
face working and also on fusion method (tsipegatuve, duration
of fusion~_ Photocells produced at 330 - 340 0 (for Cd) and at
380 - 420 C (for In) and at a fusion time of 5 to 10 minutes
were the most sensitive ones. In the case 0t illumination by
means of one of the above lpht sources, the photo-electromotive
force was 50 to 60 mw at 77 Ko A graph shows the temperature
dependence of the photo-electromotive force for 5 samples with
various donor concentrations. The purer the sample the lower the
temperature at which the sharp drop of the 'Photo-electromotive
force begins. At low illumination intensities, the photo-elec-
tromotive force depends linearly on this quantity and tendo to
Card 2/3 saturation in the caao of high illuminatiorl' inton*ities. The

67302
$07/181- 1-6-7/32
Production of a Valve Photocell of InSb With Fused n-p Junction
discussed n-p junctions have a weakly rectifying affect. The
voltampero characteristics for two ph6tooo],1s asoortained at
the temperature of liquid nitrogen and direct current b~r means
of the probe method are illustrated in a graph. The rectifica-
tion coefficient is 3 to 4. The authors th1hak the leader of
the laboratory D. N. Nasledov for his interest in the present
work and for some useful adyiae. There are 4 figures and 7 ref-
eren,ces, I of which ia Soviet.
ASSOCIATION: Leningradskiy fiziko-tekhnicheskiy inatitut All SSSR
(Leningrad Institute of Physics and Technoloig of the AS USSR)
SUBMITTED: July 30, 1958
Card 313

1-8 8-5 2~ SOURCE 675-16-0 /1-04-9F10-53
ACC-M477M CODE: 076'~477 2W0 6
AUTHOR:' Azimov, S. A*; Beter, Too V.; Gul,,iezov, U.,G,,; Yeroisil ina., L,3vin,
ORG i Iw- tituto of Eluclear Pbysioa. AN VzSSR (Inatitut yadernr* fizi~d AR UzSSR)
TITW- Cohore4-;inelastic iAteractionj Cetwoon high-enorg7 pri sup tmLnua msons mid
heiwy nuclei in Wtoemulsions ghis paper -ings given at the 14th Annual Conference on
Nuclear " Spectroa TTWMA,; February 1964/
SOURCE: Yadernaya Mika, v. 2, no. 6, 1965, io4g-1053
TOPIC TAGSs pi moon, heavy nucleus, inelastio,intoraction, plon, nuclear OnLuion
ABSTRACT: The characteristics of interactions asouiad to be the coherent
',inelastic reactions V + A -tr* + ir- *,r/-*Al an heavy nuclei in a
'phGtoemulsion are investigated,for 17.2 Gey/c primar7 pion moa~mta- The
cross-section -of this process is tound to.be 3*4 -,01*4 mbne Compared vdth i
,the corresponding value for carbonj this Indicates a dep to of the
crops-section on the atmic mmiber of the type A10W or A '0 1 0* art. ha~iz 5
figures and 8 formLlase fused on O'luthorif Engi abstA 'th-RiT
SUB CODEt '20 SMI DAM 17Apr65 / ORIG REFt 003 / OTY REFt 012.

I "
~TEROKHIXA, N.C. sladshiy nauchnyy sotrudnik
UsIng divided charges with air space at the "Lebodill-opon pit
mine in the Kursk. Magnetic AnomaV .. Vzryvo'del.o~no~~4/111
2"-246 164. ?ERA 170)
1. NIIKMA.

)2ROICIIIIA,11. 1161 L01-,ZZGMl,, K. G.~, BULHOM) A. 1. WSW
Tick Hickettsiosio Foci in Ilovonibirskayn Obloottil Z~Xlu of TOMBI.
:~Jst. Of Vaccines and Sera 110-7) PP 153-159) foUnd Ill LtLltfl. 'I'llrazitol. i
Forazitar. Bolez., Vd- quarter, 19q6.
AM: 1391

KOTELYANSKIY., E. 0. 1 dotsent 1_ BROKE NA j N. N. _yradh
Ggnical aspecte and; treatment of neopUaW of- 04 llxbMS W4
cornea. Oft. zhu. 115 noill.134-238 160# (HIM 14S 5)
1. Is Uzbgorodokoy oblastnoy bollnitaye
(~V-TUMOFJ)

MIROXHuL, o.
How the coots of gralu'reoelylag d"ots sam cOll"asatedo Dm I
kred. 16 no.5t53 Wr 158. (miiu nt6)
(GrAiR trEtdG) ii

S/136/62/000/004/001/004
zoai/z435
AUTHORS.' Berengard, A.S.,-VLl1komir*kLy, I.Ye.,
Kozhemyakin, V.A., S_edykh, T.$ LA
TITLE: Study of the chlorination of loparite concentrate
PERIODICA:L: Tavetnyye metally, no.4, 1962, 56-61
TEXTt Resulta*aro given of investigations carried out to
improve the process of chlorination of a loparito concentrate by
using the apparatus for "dry" fractional condendationiof tho
volatizablo chlorides. The loparito or* used*contained
36.2 to 36.5% TL02, B-45 to 8 55% Nb 0 i 0-55 to 0-579 T&205-~
0
28.64 to 31.18% total rare sa;th,, f.91t 3-0416 F02 O~
0.87 to 4.76 % A1203 5 to 5-87% S102, 9.86% N42 + K20,
5.94 to 7.92% CaO, ;.,'5%* P. A dry meth:d is superior to a
wet meth,:d because, for separation of t6a pulp,,there'ls no need
to use complex apparatus which has to a *rate inside aggressive
~media. The ore in crUshed, briquatted with coke and;-.
Ichlorinated. It is shown that for chlorination jt:jj~ possible to
us* a chlorine-air mixture containing Up to'35%*&Lrl~ Thia
correspomda to-the composition Of anode chlorine Sam.: It Id
Card 1/2

s/i36/62/000/004/001/004
Study of the chlorination ... Z021^435
possible to lower the carbon content of the coke brIqU4ittes from
18- 20 to 12- 13% (using concentrated chlorine) whi4h~tisrmi-ts
reducing the quantity of furnace ash,by a factor oC;a6vut :five$
increasing the production of the fur"c*, decreakeint,Ois
consumptioh of coke by 30% and increasing the coefticiont cif
utilization of the working space by 614.
There are 1 figure.and 3 tables.
Card 2/9
ON i

.................. ..
BWNGARD, AA; VILIKONIMIYO I.Y*,j KOZHBWAKIN, V.A,,;~ SEDYIM, T.S.;
YUMBINA., 0.1.
Investigating the chlorination process of loparitoe concentrates,
TS"to not. 35 no.406-61 Ap 162. (MRA 15:4)
(Chlorination) (Ioparits)

kc NR'
AT7001920 SMCZ 00081 UR/30,11)/66/000/017/0055/0058
AUTHM: Berlyand, 0. So; Yerokhtneq Its A.1 Kolacbevul Z, A.~
ORG: none
TITLE: Exchange oil air masses between the stratosphere and tropeopher* in the
M)rthern Hemispheris
M)URCE: AN $81R. lootisichookly bossitoi., Goollsichookly
33-38
TOPIC TAGS: atmospheric circulation, stratoophereq troposphere, atmospheric
temperature, tompoirature distribution
AMUM This article presents the results 04 641mvest4otion ~f the mechanism of
exchange of air immoses betum the troposphere and strato To for given 10"11
sinual zonal distributions of temperature to the 0-16 1km or and the di;Wribution
of atmospheric pressure on tbe'Rarth9a surface by finding !Wtod velocity field for
determining the vartical. imptlon of air masses, It was calculated that during a year
am air moo weighbmg 3-1014t, which amounts to 32 of the weight of the antirs. atmo-
ophare, 'descends f-we the tropopsuse In the 23-3502 sone. The weight of the 10-
16-km air layer aimmusted to approximately 1/6 of the weight L*.f the entire atmosphere
Thus, It to couclubed that sulsonge of the entire air was Utmost thA tVo"$P%4"
and stratosphere occurs within Acut. 3.5 years Is the 25--3$4 region. Ori$. art.
Cmd .112

~q

ANUOHIN. T.A,,# red.1 BUGAYWED# P,I*# redol Ilk$ Pokot m4*1
I wtodo
XM:EWV, - T. Z. t "d. GXWIWAv G*T=1211011. rt,14
[Natlwal sones and egricultwml goograpb*. of "~Let, T*Mns-
carpathia; collection of arti.aloij ftirodnmlo~,."s,red4' I goo-
grefUs sellskoco khostaistya Mweti Win';
sbomik statel, Hoakwa, 1939* '193 (KDA 12tlO)
(Transearpathia-nWolcal gecaaphy)
(Transcarpothia-Agricalture)

AUTHORS: Rogovin, Z* Awp Davydov, A.,N., Tearfin, Ia. A. 64-1-4/19
Varozova, He Ve Yerokhi 0.
TITLE: Rapid Method for the Acetylation of Cellulose in a Homogen
neous Medium
(Bystryy metod atsetilirovaniya tsellyulozy v gnmogennoy
srede)
PERIODICAL! Khimicheskaya Promyshlennosti, 1958, Nr 1p PP. 17-2o (LISSR).
ABSTRACT: The cellulose acetylations which have hitherto been carried out
in plants took from 8 - 12 hours. Therefore it was necessary to
find a method of shorter duration. In the present paper a rapid
method is suggested which refers among other things to some pro-
posals of Thomas (reference 3) as being staperfluous, so e. g. a
pretreatment of cellulose with concentratedurea solution. The
usual activation with glacial acetio acid at 6oQC for 3o minutes
is sufficient. Investigations of the influence of the acetyla-
tion temperature showed that a temperature of 7oOC is not to be
surpassed and that with a quantity of 0,3 percentages by weight
of sulfuric acid as catalyst at 8oOC the triacetylcellulose can
Card 1,13 be obtained within from 2o - 3o minutes. In order to obtain

Rapid Method for the Acetylation of Cellulose
in a Homogeneous Medium.
triacetyleellulose with sufficiently highimolecular weight
special attention must be paid to the coMpoeition of the
mixture to be acetylated. Experimental rebialts show that the
decomposition of the obtained acetylcellulcee is proportional
to the added quantity of acetic acid., on the other hand, how-
ever, the procedure becomes too expensive in the case of an
increase' adcUtion of acetic anhydride., except the prod'act is
isolated in an arid medium so that no hydrolysis of the anhy-
dride can occur. On-the strength of various investigations a
mixture of 5o - 6oo/o of acetic anhydride axid of 5o - 4oo/o
of acetic acid was found to be the optimum condition. In in=
vestigations of the catalyst quantity and its character it was
found that the quantity must be reduced at increased temperature
(from 1 - 1*5*/o to 02301o in the case of sulfuric acid), aniline
sulfate (0,6 percentages by weight) is asstimed to be a better
catalyst than the ammonium sulfate suggesfAid by Thomas. Tho inm
voatigationa arc carried on in order to twat ttlam in the indu-
strial scale and to obtain a further roduction of the acetic an&
hydride quantity.
Card 2/3 There are 3 tables, and 3 references, 2 of which are Slavic.

Rapid Method for the Acetylation of Cellulose 64-1-4/19
in a Homogeneous v4dium
AMOCIATrONZ Laboratory of the unpp at. the Chemical Plant Vladimir
(Laboratcriya, NIIPP i% VlAdimirsims khlmichw?~; zavods)
,mrAUMLE18. LIbriI7 Of COUV=6-
1. C611doso-Acetylatia
Card 313

SHCHERBAKOV, V.G.; YEROKHINA, V.L.
Effect of a prelizinaz-f treatment on the biochemical processes in
the storage of rice bran. Izv.vys,ucheb.zav.; pishch,~tekh. no-5:
19-23 1630 (MIRA 16:12-)
1, Kramnodarskiy politekhnichookiy inatitut, kafedra takhnologil
zhirov.

JMMM B.Aq ORWHINUU,, L*A-;
bitemation of 2j,3-dimOtb71X+A41GnG'~ with othyleae* imid *"laco
::4*2
ablorophavOitem, rw, AN SM. OtdAhim.mauk nb~U 076
N 162, MMA 15M)
I* lasemkiy goaudarotmMy wiversitert im. VT, ultyagove...
(Ifttadiens) (Ithylins *ophits)

Mum-
I It
ACC Nat ;'kP001-077
L. A~ Y~roW na j1%
Arbuzov B. A.; !~Ltapshinsk
4-110-711,10 1
Ya~-Aanw University im. V. 1. UV;~dhav -LenjxL nryv
Un'
Lver*itet)
H.;Iz: -interaction of cyclic chloropn__~iA~th dient),*0~1roei"bons
1961; .1820-1826
1 SMFLE: AN SSSR. Izvestiya. Seriya khimicheakaya no., I
TOPIC TAGGS: phosphorous compound, chlorine oompound, con~q!gjLtedj'olyoiefin iydrocarborl
chemdeal reaction
'(;~B -pjr,- - The interaction of ring chlorophoiphites 4ith ti~q;M-' .61 diene
I rste"M f both linear and cyclic structure wads investiga~q II. Uo; addition
of 2 -bltylene- and 3-chloroprop7lenechlord~hos~hites )~-h
0 xadiene
,3 1 1 t
and allo.ocimene wAs accomplished. All ~ of the' reactions, tzidi pl;-_c'~_by &e
SaTie mechanisn, and undergo the Arbuzov rearrangement tes4~ ikg i# iiub3ti-
tuted phospholinoxides. The characteristics of the obt&iz~O I': subil,tituted-
3-phospholin-l-oxides are presented,
Such reactive dienes as cyclopentadieneand anthirac do n V~eater
In'to the diene synthesis with rin4'; clA6ropho phites.
Yalic ~oOeeds
1 The reaction of ring chlorophosjohites with aq, die' +S P)
1 quite difficultly and does not occur.-4AW&~or dieneA (00 iperaadiene
1 .3nd anthracene). The most reactivering qhldroph Iosphitea) ~thei J~Vfia;:tions
jDjj~ 5112'j914
LCard 1/2 661.71113.1
I A

L~ 20353-66 1
ACC NR. A 012077
mith dienes are the pyrocatechinchloro(bromo)~hosphiteo whi i rea~-t with divinyl
wrasually readily at room tergerature and witbout,~a ca-talki Thi 6haracteeistics
of the obtained products are presented.: the i~th6rlis tbankil G. Lztkovan for taUng
4GT
the IR-spectra. Orig. art. has: 2 tables', [41R~]
13UB f E: 07 ME UTE: llJul63 9~14:REF 003 ;~CTR IfOIT: 003
ODE

HXH&A V.N.-,- VEMER., D.D.
PotentUtion of bypnic inUbition by mans *of a ammU-sixed aimplified
apparatus for electrons cools. Trudy Gos. nauch...d.wl Ipoilchonevr.
inst-, no.241167472 161. (MInA 15:5)
1. 2-oy pe.iWatrichookoys otdel~niye i'eksperimintalInap gruppa
po razrabotke meditaindkogo oborudovaniya Gosudaws-tvennago nauchno-
is8ladavateliskogo psikhouevrologicheako o instituta, imeni Bekbtereva.
(ELECTRIC ASESTHESM

YEROKHINA. V N
I
Electric sloop therapy In Astboxic and depressive istaUs. Vop.
Paikh.i nary. 8071-377 162. (MM 17:4)
1. Psikhiatricheskaya klinika. (zav. Yu.A.Povorinskiy) Leningradsleogo
nauchno-issledovatellskogo Psikhonevrologicheakogo instituta imeni
Bakhtereva, (dir. - B.A.Lebodev).

AUTHORS: Yershov,
T IT LE: oatalytio
Olefins
PERIODICAL: Izvestiya
19609 No-
B/06Y60/69D/OQ8/O25/O33/ZX
B013 B0551
ff. I., Yerokhina,,V. R.1 and Bydus,.Ya. T.
Isomerization of-Gycloprop~ne iii MizIures With
Akademii nauk SSSR. Otdeleniye 1th,1mi*h0ok1kh nauk,
89 PP- 1495-1499
TEXT: In the present paper, the authors studied the efftiat of admixing
cyclopropane to ethylene and propylene on their polymerization over various
catalysts. Cyclopropane was prepared by the method describedi,by G. G.
Gustavson (Ref. 11). Quantitative determination of the -propylene and cyclo-
propane mixtures was carried out by a method based on the selective ab-
sorption of propylene in a KI-Br solution (Ref. 13). The apparatus and
2
experimental technique was the same as in Ref. 15. The following catalysts
were applied: Cobalt on alumina (Ref 16) (1), silica g~a- (u), cobalt/
silica gel (III), aluminum silicate 4V), and cobalt/aluminu.in silicate (V).
On catalyst M neither ethylene nor propylene formed liquid polymeriza-
1 0
tion products at 300 C and below. Addition of cyclopropane (7 - 30%) to
Card 1/3

Catalytic Isomerization of Cyclopropane S106 60100010081025A31XX
in Mixtures With Olefins B013YBO05
ethylene produced only slight formation of liquid polym~rlzaiea. The
yield was less than 1% of the initial ethylene and 9 - it3% of the added
cyolopropane. The latter was isomerized only up to 20% (Table 1). In ex-
periments with pro ylene (Table 2), the portion of reacted oyclopropane
was lower (5 - 15Z. The data listed in the table shov,that liquid poly-
merizates are formed in small quantities,or not at all9 j1heDL cyolopropane
is added to ethylene or propylene. The cyclopropane is Isjomsr:ized only
vlightly, only up to 20%. in the presence of hydrogen, the yields of
liquid hydropolymerizates of ethylcrne) obtained with and without addition
of cyclopropane, did not exceed 4.1% of the initial alkene. The addition
of cyclopropane did not affect the yield. 33 - 57% of the cyclopropane
antered into reaction, i.e., a much higher per,3entage than In the absence
of hydrogen. No liquid polymerizatee were formed in experime .nts employing
catalysts containing aillca gel, (II) and (III). Neither pr4yiene poly-
merization nor cyclopropane ioomerization occurred. In tests employing
catalysts of propylene polymerization which are based on synthetic alu-
minum, silicate, the cyclopropane in mixture with olefins is isomerized
155 - 100%- It was stated that no final conclusions concerning the poly-
merizing effect of cyclopropane admixtures could be drawn froin the ex-
perimental data, since the yields of liquid polymerizates were lower than
Card 2/3

Catalytic Isomerizatlon of Cyclopropane S/062/60/000/0()8/025/033/XX
in Mixtures With Olefins B013/BO55,
the amount of reacted cyclopropanoo It was, however, posmible to determine
the activity of the,various catalysts. Cat 'alysts oontaining aluminum
silicate were found to be very active in i aomeiization of eyalopropane
in mixtures with ethylene and propylene. Cobalt on alumina was much less
efficient. There are 4 tables and 22 refefences: 12 Soviots 10 US,
1~ British, 7 German, and I French.
ASSOCIATION: Inatitut organicheskoy khimii im. ff. D. Zelinskogo Akademii
nauk 85SR
(Institute of organic Chemistry imeni N. D.. Zelinakiy of the
Academy of Sciences USSR)
13
UBMITTED: March 9t 1959
Card 3/3

S/026J'60/-133/01/50/070
B01111'003~
1UTHOASt Tershov, N. I., Eydus,,Ya. T., Torokbinap V. P.
TITLE: Oxygen-initiated Polymeri2ation of to bV ffeterogeneous
Catalysis in the Presence of Hydrogen .
PERIODICALs Doklady Akadsaii nauk SSSR, 1960, Vol- 133, No# it
pp. 108-111
TEM In a preceding investigation (Ref. 1) the authors have found that
ethglene is polarized on a Co-olay catelystlduring hydrogenation at
100 C. So far, such a polymerizati; had not been observed if the gas did
not contain 00 Impurities. It was proved that polymerisation at 1000C
is not initiated by 00 but by oxygen. This reaction is reduced by a rise
In temperature, and is most vigorous between IOD and:12000. It is
additionally intensified by an Increase in the oxygen content up to 2%.
It does not take place in the absence of oxygen and 'hydrogen. In the
article under reviewq the authorereport on son* reau. 'Its of this new
reaction named in the title. The same apparatus and cittalVat were used
as in Refs I and 2. Table I lists the experimental re'nults obtained at
Card 1/3

81720
Oxygen-initiated Polymerization of Ethylene by 8/00/60/133/01/30/070
Heterogeneous Catalysis in the Presence of B011/11003
Hydrogen
a ratio of It3.2 between C H and 9 It may be soon ilhat ~olymeriza-
2 4 2
tion yields a gaseous dimer and up to ~5% of liquid products (referred
to the ethylene used). The waste gas contains 1-1.5f.'of CO. The authors
assume that the said reaction is identical with the hydropolymerization
of ethylene under the action of 00 (Refo 2). This was, hooever, not the
case since the reaction did not give the highest yield between 190 and
2000C and was not intensified with rising CO concentra.tiot. Table 2
proves that this is the case with 0 2R4 t a2 a 1.1 and an 02 content of
2%o At the same timeg the ethane yield rises from 45 ,to 79%, Experimental
results obtained at different temperaturesp which shoir tho effect of CO
additior. upon polymerization and hydrogenation, are giLven in Table 3.
The presence of CO and R 20 in the waste gas and the reaction water of
several experiments indicah that 0 2 added to the reaction mixture
reacted vigorously with the main components.during tba reaction. The
authors assume that active surfaces are thus formed, which initiate the
polymerization of ethylene. This is proved by the izoreasing quantity of
Card 2/3

61720
Oxygen-initiated Polymerization of Ethylene by 5 0207 60/133/01/30/070
Heterogeneous Catalysis in the Presence of 110117111003
Hydrogen
reaction products with rising 0 2 content at 1000C. ftook all this the au-
thors conclude that the reaction named in the title is initiated by 02*
The polymerization of ethylene in the pree nee of E ill not
identical with the hydropolymerization und:r the aohon of 00. There
are I figure, .3 tables, and 4 referenceso 3 Soviet and 1 German.
ASSOCIATIONs Institut organicheskoy khimii is. N. D. Zelinakogo
Akad*mii nauk SSSR (institute of Organio'chem .Istry Imeni
X. D. Zelinskiy of t~e -Academy of Sciences, U38R)
PRESENTED: March 10, 1960, by B. A. Kazanakiy, Acadenician
SUBMITTEDs March 8, 1960
Card 3/3

-YERSHOV, N.I.; EYDUSp YU.T,: YEROXHINAg VAL.
Catalytic t7drocondensation of carton monoxids,r4th olefins and the
hydropplymerization of olefins under the effect of onrbon monoxide
and hydrogen. Report No.32: Conversion of I-octene. Izv. AN SSSR.
Otd.khim.nauk no*9:1696-1702 S 161. (MIRA 14:9)
1. Institut orgenicbeekoy khtmit im. N.D.4114kogo AN SSSR.
(Carbon mnoxide) (Oatene) .~(~jdroffen)

8 .
SA116121),61 /000/010/010/01 a
B106/Blol
AUTHORSt Yershov, N. I., Eydua t Ya. T. , and 1 "raunfL. VR.
TITLEi Catalytic hydrocondeneation of carbon monoxide with olefins
and their hydropolymerization under th~ action of carbon
monoxide and hydrogen. Communication 33. Formation of
higher hydrocarbons with a number of carbon atoms not being
an integral Multiple Of the initial olefin
PERIODICAL: Akademiya, nauk SSSR. Izvestiya. Otdoleniye khimicheskikh
aauk, no. 10, 1961v 1871-1874
TEXT: T4e catalytic hydropolymerization of olefins under the action of
carbon monoxide in the presence of hydrogen and the hydrocondensation of
carbon monoxide with olefins yield both real polymers wid their hydro-
genation products, and a considerable quantity of higher hydrocarbons with
a number of carbon atoms not being an integral multiple of the initial
olefin. The authors clarified the reasons of formation of these higher
hydrocarbons. The yield of theae hydrocarbons increases with increasing
Card 1/4

2P,1273
S/06%61/000/010/010/018
Catalytic hydrocondensation of carbon... 'Blo6/ 1101
molecular weight of the initial olefin (double bond In 1-position) while the
value of the mean multiple K decreases for the whole higher-boiling frac-
m
tion of the condensate. K m . (5- aini)/n (2) (cti - fraction. of the i-th
hydrocarbon in the higher-boiling fraction of the coadensote; n. - number
of carbon atoms in the i-th hydrocarbon; n w number of carbon atoms in the
initial olefin). The formation of larger amounts of higher hydrocarbons,
the carbon number of which is not an integral multiple of the initial
olefint can be explained neither by hydrocracking of the initial olefin nor
by its hydracondensation with carbon monoxide. Therefore, it is assumed
that the formation of the higher hidrocarbons mentioned is due to the
cleavage of carbon-carbon bonds during h-!-dropolymeriz'ation or hydrocondensa-
tion. Radicals are formed which may lead to the formation of higher
hydrocarbons with a carbon number not being an integral. multiple of the
initial olefin. The authors concludes In catalytic roactlans of olefina
under the action of carbon monoxide and hydrogen, the kiydrocarbon chains
grow less by molecular interaction of the initial olefin than by reaction
Card 2/4

2,8273
,/.61/000/010/010/018
S/062
Catalytic hydrocondensation of carbon... B106/A.101
of the initial olefin with radicals formed by oleavago of carbon-oarbon
bonds on the catalyst. Therefore, the higher-boiling reaotion products
mainly yield hydrocarbons the carbon number of which is not an integral
multiple of the initial olefin. Hydrocarbons with f6ter oarbon atoms than
are present in the initial olefin are also formed in small quantity. The
cleavage of the C-C bonds is facilitated by plane addition of the absorbed
olefin molecule to the catalyst surface and the resulting deformation.
This plane absorption only occurs at low carbon monoxide concentrations.
At higher concentrationsp the carbon monoxide may displace, from the
catalyst surface, the carbon atoms of the olefin which do not lie at the
double bond. This eliminates the deformation of the,olefin molecule.
Under such conditions, the hydrocarbon chain may grow -without cleavage of
carbon-carbon bonds by hydrocondensation of the olefin with the carbon
monoxide accordinc- to the following schemet
CH2-CII2 + CH 2 ) CH 3) CH-CH2
CH.$ CH-CH2 + CH2 0 CH3 CH2CHwCU 2) etc' (3).
Thus, the type of adsorption of the olefin molecule and., therefore, also
Card 3/4

28 1
S100/61 ~(0700/01 0/010/01 a
Catalytic hydrocondensation of carbon."# B 106/11101
the direction of the reaction may change as dependent on,the content of
carbon monoxide and hydrogen in the initial gas mixture and on the
capability of the olefin of being adsorbed. These reciprocal transitions
of the reactions of olefins under the action of carhon monoxide and hydrogen
will be thoroughly studied in the following communioation. There are
8 referencesi 7 Soviet and 1 non-Soviet. The reference to the English-
language publication reads as follows; A. W. Pletcher, 14. J. Gibson,
Radioisotope Conf. 11, 41 (1954).
ASSOCIATION: Institut organicheskoy khimii im. X. D. Ze,lJ.nskogo Akadeinii
nauk SSSR (Institute of Organic Chemistry ~roeni
N. D. Zelinakiy of the Aoadsmy of 3dienceo. '133R)
SUBMITTED; April 8, 1961
Card 4/4

SIO 42~~611000101010111018
Q
B106/B101
AUTHORS: Eydus, Ya. T., Yershovt N. I., and Yerokhina., V. R.
. ....................
TITLE% Catalytic hydrocondensation of carbon monoxide with olefins
and their hydropolymerization under the action of carbon
monoxide and hydrogen. Communication 34. Reaiprocal
transitions of formation reactions of hydrocarbons from
mixtures of ethyleneq hydrogenp and carbon monoxide
PERIODICALi Akademiya nauk SSSR. Izvostip. Otdsloniye khtmiaheakikh
nauk, no. 10, 1961p 1874 - 1879
TEXT: It had been assumed previously (Ref. Is N. 1. YerAhov,
Ya. T. Eydus, Dokl. AN SSSR, 115, 1126 (1957); =, 1062 (1958)) that one
stage of the synthesis of higher hydrocarbons from carbon monoxide and
hyd.rogen is a radically proceeding hydrooondeneation of carbon mono;Ude
with olefins. In the subsequent stages of synthesis, thia reaction may
change into a hydropolymerization of olefins, which constitutes a radical
chain reaction. In the present study, the authors considered the
possibility of' a similar transition of these reactions into each other on
Card 1/5 A

2M274
S10621611000101010111018
Catalytic hydrocondensation of... B106/BIOI
a catalyst thatio efficient both in the reaction aocording to
Orlov-Fischer-Tropoch, and in hydropolymerization r'oaotlons of olefins and
their hyclrooc-ndeneation with carbon monoxide. Such a. catalyst was obtained
by activatine: a Co-clay catalyst with addition of 1$% Th02 (referred to
metallic cobe,lt). A Co-kieaelguhr catalyst is also catalytigally active
in all reactioIno mentioned. The tests were conductsd at 190 C and
atmospheric pressure in a flowing system. The volume velocity of the
initial gas mixture was close toolOO hr Before the tests, the catalyst
was reduced vith hydrogen at 450 C for 5 hr; the catalyst was regenerated
in the same manner. Binary mixtures 00 _ H2 (1s2) and ternary mixtures
C2H4 - H2 - CO of different compositions were used 4's initial mixtures.
No liquid hydrocarbons but mainly CH4 $ 002' and H20 were formed in the
tests with binary mixtures CO - a, dur ing the first 5-7 hr of the reaction,
immediately after reduction of the catalyst. The same occurred
immediately after regeneration of the oatalysto The formation of liquid
hydrocarbons Dnly begins after 6-T hr contact timej1heir yield grows from
Card 2/5

.OpM
s/o6 0/000/010/oll/ols
Catalytic hyd:rocondeneation of... B106Y)3 ioi
one regenerat4.on to the other (Fig. 1). Initial mixtures with 7-7.5~* CO
and with 25-35fo CO were used in tests with C 2H 4 - H2 " CO mixtures. At
lower CO conceintrations under otherwise equal conditions, the yield of
liquid hydroccrbons was 2-3 times the yield at high CO concentrations.
In the presence of small CO amounts the ethylene hydrapolymerizes, at
higher CO concentrations hydrocondeneation with carbon morioxide occurs.
Thus, it is possible to attain a transition from one reaction into
anothery and vice versa, by changing the composition of the initial gas
in the presence of the catalyst. A reduction of the C 2H4/H2 ratio in the
initial mixture favors hydrogenation of ethylene to ethane. It was found
that the molar ratios at which CO, H 21 and C2H4 react with formation of
liquid hydrocarbons are -very similar to the molar ratios of these gases
in the initial mixture. Fig. I shows that hydropolymerizatioA and
hydrocondensation in ternary mixtures also proceed in the first 5-7 hr
after reduction or regeneration of the catalyst, and even produce
maximum yields of liquid hydrocarbons in the period of regeneration. The
synthesis of hydrocarbons from CO and H 2 , however, yields only methane
Card-3/5

2627h S10612/61/000/010/011/018
Catalytic hydrocondensation of... B1067,3101
at the same stage. This interesting fac.t may be explained as follows:
In the synthesis of hydrocarbons from CO and H 29 the xeduction of carbon
monoxide produces radicals which either polymerize (inothylene radicals)
or condense, eog., with cleavage of water (hydroxy methylene radicals).
During methane formation at the beginning of contact, the interactions
of radicals are apparently hindered so that the radicals act on the
adjacent particles (hydrogen in binary CO - H2 mixtures, olefin in
ternary olefin - CO - H2 mixtures). Thus, the same factors that effect
methane formation in the synthesis from CO and H 2 favor, in the case of
ternary mixtures, the hydropolymerization of olefins under the action of
small CO amounts and the hydrocondensation of CO with olefins. In this
case, the methylene radicals do not associate but are prenerved as
reaction centers and reaction initiators with the hell) of olefins. There
are 1 figure, 3 tables, and 10 references, 7 Soviet and 3 non-.Soviet.
The two references to English-language publications -road as follows:
E. F. G. Herington, L. A. Woodword, Transo Farads. SOC. 11. 0158 (1939);
S# R. Craxfordq Trans. Faraday Soc. 3Jv 947 0939~.
Card 4/5

20274 7062/61/000/,10/011/618
Catalytic hydrocondensation of... B106/B101
ASSOCIATION: Institut organicheakoy khimii im. N, D. Zelinskogo Akademii
nauk SSSR (Institute of Organic Chemistry imeni
N. D. Zelinskiy of the Academy of Sciences USSR)
SUBMITTED: A~ril 8t 1961
Fig.l. Various types of formation reactions
of hydrocarbDns and their reciprocal trans-
formItion. Legend: (a) hydrocarbon yieldq
ml/m ; (b) hours; (1)p (1a)q (19)t and (18)
synthesis of hydrocarbons from CO and H.;
(2) and 1,2a) hydrocondensatibn of CO
with CA[ (initial mixture contained 25~6 CO);
(3) and (3a) hydropolymerization Of 02H4 under') 14
the action of CO (initial,mixture contained
0 to 40 60 Wvrv
7-7-5',!) CO); the vertical broken lines
indicate the instant of catalyst regenera-
tion.
Car& 5/5

310621621000100510061008
B110/3101
AUTHORSs Yershov, No Lg Sydus, Tat Tot and Yerokkina#,V. R.
TITLEs Gatalytio hydrooondensation of carbon monoxide with olefina
and their hydrdpolymerization under the adtift of carbon
monoxide and hydrogen- 36. Hydrooondeneatiot and
hydropolymerization of olefins on the nickel catalyst
PERIODICALs Akademiya nauk SSSR. Izvestiya. Otdoleniye khimicheskikh
nauk, not 5, 1962t gii-gi6
TEM The specific character of the nickel catalyst (as compared with the
cc catalyst) was examinodi and the hydropolymerization ofethylenet
propylenet and butylene under 00 action was tentativalv per.'rormed on it.
The catalyst was Ni-Mn-Al 203 kieselguhr (100t2000000). However, the
synthesis of liquid hydrocarbons from ICO+2H 2 (200*0) does not set in
3
until after 20 hre. The yield first attgined 12e M then 145 ml/m
while 'What of CO2 and CH4 dropped to/v1O and 20-2;V..3W'ith 15-18A
additiqn of ethylene to 100+2H., liquid hydrocarbons4ormed in the
Card 1/4

3106Y621000106 ~/006/006
Ostalytic hydroconaensation of carbon B11 0 B101
first hours already underev75% hydrogenation of ethylene. This is
brought about (I) by dilution of the initial CO-9 2 mix ture with ethylene
which# in reducing the reaction ratep also reduces the.catalyst heating,
and thus inhibits the methane formation; (2) by preferred ethylene
adsorption to the most active catalyst centers, at which the methane
formation takes place.. Since the hydrocarbon formation, from carbon
monoxide and hydrogen in the presence of ethylene takett plaoe at the
less active catalyst centers, liquid hydrocarbons are immediately formed.
Ethylene isImost readily hydrogenated on the catalyatt at 1000C, the
process was almost as rapid as at 200 0C9 the yields of gaseous paraffin
hydrocarbons being 25-27A at 100 0C, and 29-4A at 200000 1. At 19CI-2000 0
on the Hi catalyatt ethylene chiefly reacts with hydrogen, an the latter
cannot react with the products of incomplete 00 reduotion. Xfp however,
this is made po'asiblb, othylene can take part in the synthenis of higher
hydrocarbons. Thus, when-& binary mixture of ICO+2H and ethylene waa
alternatingly blown through for 3 and 6 mint respectively-, the yield of
liquid hydrooarb~ns was 240-260 ml/m3. 60-68% of reseting ethylene is
Oard 2/4

S/062J62/000/005/008/006
Catalytic hydrocondensation of carbon B110/3101
hydrogenated to ethane. When alternatingly blowing,through with
propylene (6 min) and ICO+29 (3 min)v the hydrocarbon yield was raised It
2
3
to 154-172 ml/m3p i. e,, it rose by 60-79 ml/m as oompired with the
binary mixture. The propylene hydrogenation was relatively poor in this
connection (17-5A of initial propylene). When alt~rnatingly blowing
through with butylene (~ 'min) and ICO+232 (3 min) , *he olefin yield rose
to 210 ml/M-3, and the yield of gaseous paraffins dropped to 9-10A of
initial butylene. When blowi ,ng through with ternary miXturoa of Cot 1121
and olefin (9thylenet propyler,*0 butyleno) at 19000 an&an atmospheric
-1 : LIZ
preosure with -100 hr volume rate on the Ii. catalystp the Olefin is
hydrogenated to the corresponding paraffin* The formation of higher
hydrocarbons from CO and H2 in the presence of ethylene and its homologs
takes place at 190-2000 0 on the catalyst surface which is free from olefin
molecules. This surface is the smaller the higher the olefin
concentration in the initial gaseous mixture. This, causes the yield of
liquid hydrocarbons to decrease on olefin additiqn. lf,.however, the
olefin reacts with reduction products (methylene and other radicals),
Card 3/4

5/062/62/000/005/008/008
Cataly#c hydrocondensation of carbon B110/B101
hydropolymerization ancl hydr ocondensation prevail oyer,olofln hyarogenation.
There are 4 tables.
ASSOCIATIONs Institut organicheakOy khimii im, No D. Zolinskogo
Akademii nauk SSSR (Instituts ot Organia4hemistry Imeni
N. D. Zelinskiy of the Academy of soienoes USSR)
S'M.'ITTF.Dt -December 16, ig6i.-
Card 4/4

MUSO 7&.T,l YERSHOVp N.I.; MMaNAt V.R.; ANDRUBVo N.-S.
Gqgen-initiated haterage"Ma caulytic reactim af'oondeasa-
tion of olefins in the presence Of l7drogen. Part 2 tConversions
of etbrIene. M. - L kat. 4 to. 31416-Ql M;-Jo ~ 163.,
: (MMA ~637)
1. lastitut organtahesko khisdi! imni Z*Hnsk4o AS 962.
(Itbylene5 (polmrizatlon)
(ftygen)

YERSHOV, N.I.j SYDUS0 YaTmj Y&ROXHIRA, Me; AMIRSYSVt N.111,i
Oxygen-initiated heterogeneous catalytic reai.-tion; of 1:on-
densation of olefins in the presence of bydrq,,en, Part 3s
Conversions of propylene. Kin. i kat. 4 no,,,6':029-$,3/, N-D 163.
(WPA 17: 1)
1. Institut organichaskoy khimli imeni Zelinalcogo AN SSSR.

YERMOV, N.I.; MUS, Ya.T.; YEROKHINA V R.; AHDRLIEli~l lf.s,;
Oxygen-initiated beterIogemous cat~Vtic reactl~ml d condensation
of olefLns In the preseAce of hydrogen. Part 5s Cbh*rdlon ~of isobutylons.
Kin. I kat. 6 no.'2000-30,7'
Mr--4p "65. (MRA 18s7)
.1. Institut organicbeskoy1hiiii ZAINA AN SSSR.
mill

EYDUS, Ya.T.; YERSHOV, N.I.; YEROKHINA, V.R.j AIIDIBYEVj N.S.
Oxygen-initiated heterogeneous cata3jytic candentation reaction of
olefins in the presence of bydrogem, Part 43 1-Butene conversions.
Kin.i kat. 5 no.6t1063-1068 N-D 164. (MIRA l8tl)
1, Institut organichookoy khimii imeni Zolinokogo All 158SR,

DOBRI)SHKOP D.B.; I'Maimali uchustiyej.~ OKIMEVA, [,.A.
Round aross-seption ring packingso Much, I- rez, 244 no.5; '
My 165. (1,1111A LAO)
1. Sverdl-ovskiy filial Nauchno-Isoledovatellskogo inutituva
rezJ..novny promyshlennostt.

BLINOVSKIT, A.A.; BUMVA, Y.A,; TJROKHOVj_.Ar,,_j_.IVAXIYf, IC,A.; KITAYBYA,
G.T.; LMOSHITS, L.K.; IUMTAYBV, I.A.; PALEADIMA. N.Y.:
PZT"M. L.K.-, PWR YG.D'-, Rowmry, U.N.; ImlyY9 NAO;
9MNOV, B.F.; IMNISOVA, I.S.#,red.; RAKOVp SPI*# t4ftnered.
(Through our land; tourist sites and Itineraries -Dr the mosoaw
Interprovince Tour Administration of the All-11nion Central
Council of.Trade Unions] Po rodnal senle; twistskie basy i
marshruty Koskoysiogo iseshoblestnogo turistoko-sko'kursionnogo
upravlenila MOS. Moskva, Izd-vo VTpW3 PrDfitflat. 1959.
134 pe (%IRA 13:4)
1. Moskovskoys mashoblastaoye turistako-okskursio"nore uprnylaniyo
Yeavoyusnogo teentrallnogo so-yeta profsoyuzov (for all, except
Denisoy Rakov)O
ourism) (Steamboat lime)

TIMDK3)V. 5
Flying an Au-2 at night, Graxbd.av. 13 so.8i'll Ag 1~56- (NLRA 9:10)
(jxqtr=sg4 flylog) (Airplaws)

MOKHOVO
Recent data an the composition of products of PdAdlo, Kiwene voloanim
In Mftray District (Sakhalin). DWd. AN MH' 1,37 ila,,34V-639 Mr
161. (MIRA 14P 2)
1. Sakhalinakly kompleksayy nauabno-isslodovatel'skil institut Sibirskogo
otdoleniya AN SSSR. Predstayleno akadealkam Viet.3abolviyu.
(Makarov District (Sskbs1Jn)-#AcksO IgI20OUS)

IEROKHOV) VC30
Some problems of planning design oWationst apital
and the organization of customarol capitil conatruAimn diviel-ina.
Trudy KMI no.15a4A.6-40 t61, 011RA ly+:32)
1. Irachallnik otdola kapita-Ilnogo stroitellotva Zar-q=zbskogo
sovwLrkhoza.
(Zaporothl7a-Conetruction induotx7)

GFIIBOM, B.B., kand.tokhn.nauk; YP2~Qj,.U&D.; D&MIYANYUK, V.A.
DetermWn6 the ti= and path for motor-vehicle pansing. Avt.prom.
31 no.7oll-13 Jl 1659 (MJRA 18:8)
1. Lsvovskiy politeMmicheskiy inatitu'4.

2-58-5-11/17
AUTHORSs Yerokhovetep I., Chairman and Serebrennikov, I., RWou
-Tnapeot3Y'
TITLE: On the Importqnce of Centralizing the Aegistration and Stati-
stics at the District Inapectorate of TaSU USSR (0 znachenii
tsentralizatsii uchdta i statistiki v rajonnoy inspekture
TsSU SSSR)
PERIODICALs Vfastnik Statistiki, 1958, Nr 5, PP 76 - 77 (USSR)
ABSTRACTs Information is presented on the activities of the TsSU USSR
District Inapectorate of the Altay kray, wherii the centraliza-
tion of statistics on agriculture, national education, public
health and culture was brought about in 1957. The authors
state that this new orga3iization has proved satisfactory, al-
though there are still some difficulties to be ovdftome.
ASSOCIATIONs Kamenskiy rayispolkom Altayokogo kraya (KmenskiY rV1.0olkom
of the Altayakiy lirW)
AVAILABLE: Library of Congress
Card 1/1

............. ..
TXROKIN 'P.
7,ollowlM the example of ValAmt1ft GsPwTA, lbko-elev- pros. 25
U0.11:3 M 139 (KLU 13:3)
1. Balashovinkly mmllulobM kombluisto
(Shchagoltkova, Sim DullbrIevvis)

BAGIMIEV,, Vladimir Vladimirovich; VINDXMV* Anstoliy Ivanoviabi
XISMZV,, Vyacheslar AlsksandroviW4. PANION., P~A#
Bentsionovich; ITSKOVICH, Gftrgijr. #Lkbsylovtc~j
KONDRASHOV, D.A. . insh.., rets.ensfttj WINSHKIII, A.Cs.j
insh.p reteensont; APJMSHA9 A.I. nauchn. red, KOZIAOMWOV
B.S., nauchn. red.; VASILIMA, r*461 InKnoriyA -
Ye To. red.; SH,AURAK, TeX. red.; RAIALUTA,; P.M.9 ',MMs
4kW
[Collootion of problems la toohnical 890hamcis Sboinlk sa-
dach po tekhnichemkoi sekhardkolpy) V.VA&69~v 1 4 ra Ls-
nin4pm4 Sudprougis, 1963* 551 Olt 164)
(Meahanical engineering--?" aw, exerclosi,', 6tc.0

KASBANSK31, Mikhail Stanislavovich; FINSKIYp losif Yevoi3yevich;
SOKOLOV., Nikolay Vladimirovichl ALEKSEMj, P.M. p inah.,
retsenzent; KLINI S*V.p inzh., rets9nmout;,.YMl=MWAl,-. .
Ye,Yeej, red.
[Standardization and toohnology of the mandacturn of
marine pipe fittingal Tipizatolia i tokbnologlia lzgo-
tovlenila nudovoi armaturyo Leningrad, Sudostroeoies
3.964. 317 P. (MIPA 180)

511MANDIN, Yovgeniv Mikhaylovich [deasaaed]l RAMV, 11rorl
AloksoMrovichl DYTENSKIYp LA,# kando tokhtt. nauk
nauchn. red.1 OMLOV V M Wind. tekbn. jakok,
rateenzent; YEROMITRAYA, ioJo., red.
~," -It ..z , -, j ., 7
(Cold brittleness and plasticity limit of metals In sbip-
building] Khladnolomkost' t prodeltnaia plastichnost' me-
tallov v sudostroonii. Leningrad., Sudootrooniep 1965.
335 p. 011A 1911)

YnIGMj,.,2,I,jYer'omina,, Z.1.1; WRMCHO V.G. [Bur-evyl3h,, V.H.]
Using vanadomtry to detemine orgwdo PI IHASI pmpamtiona.,
ramtsev. shur. 16 nooltl3-18 161o WRA 170)
1, lafedra analilichookoy Waii Xbar'kvvokogo,l)u-mboovti-
chaskago inotitutao

- 7=MTSKlr, [IRromWts'kyl, 041 .--
Ion exchsqprs,, the catchers of admixturts. Zswuta pratola
no.6:12-13 Js 160. (MMA 13:,B)
(Ion exchmace)

TJRMTSgff# 0. C13rwwts'W, 0*1
---------
RNI'tran.0 Snaa to pistol& w*9t22-13 3 160. (KM 130)
(ImAile fabrics, 9yattwt1c)

WOMITS 0 Mtalkyi2 0.1
Story about ?ran. ta pratsia no.10*.,22-23 0 v 61.
011RA 311:8)
(Glass manufacture)

MIGCRIM# 1mv Yakovlevich;ASTRATOVpN.A.p kand. tekbn, naukj
retsanmtj MARTOV, I.M.v kmA, tAW=, nauk# zmmobn4
rod.;-YUCMBKIU,, TO.Te', red*
Eship vessels operating under pteemrs; determination
of stresses wA deformAtiome] &AM70 sosudyp ;'VA7OOtAiUMhCbi6
pod davlenim; operedelenis napriashenii i deformateiio Le-
ningrad# Sudostroonie, 1965o 19,4 ps (MIRA 18s6)

PAPIR, Abram Nutovichl FEVZM, B.M.v retsenzentj YEFLOWITSKAYA,
-1.1-1i'll
--%-.I.."- I I ,
I Ye.Te., red.
[w&3,.flow Pumps for water-jet propel-lero] Oserje natiosy
vodometrqkh dyishiteloil onnovy toorii i raschOtAx. lonin-
grado Sudostroonlop 1965o 250 p. (14XRA

KOXICHEV, Wasutin NikolaWavlehl KOZLOVI F.V-p retsenment;
YWHITSYZA To To , redo
,
I [Noncircular joints in marine ~4i~eeringj flek.ruglya
soedino=Ua v sudovom mashinostroonli. Lenitgrad ' a!Ado-
atroenie, 1965. 216 p. (MIRA 1815) 1

1; 33-003-M FM/WT(1)/]%I?(e)/D/T(M)/P,~C(k)-2/7/W( IJP(c'
ACC NH: APW07001 W13/4WH SOME CODE: IWOR1414/011/002/0217/0218 dl
AUTHOR: AtsnyM. M.-M.; Yerlooks, V. D.: Donchkovallwyp V. T.
ORG: Institute of H~4161OWeics and Electronics,, AN Ukr0SRp rlkov (Instytut,
radiofizylw I elektroni]W AN
TITW; 1"er y1th IN= Q switching
1SOUKE: UbVIns JWy fIzychWy zhurnal., v. Up no. 2j, IWO 217-218
TOPIC TAGO: laser opticaj laser moftlationp resorAtorp;laser r and d,Q switching
ABSTRACT: Whoreas in earlier wq~eriments Q switching was usmlly effected by In-
terrupting the coupling between the aotive rod and only one resonator mirror, the
authors investigated the properties of a laser in which the coupling with bath mir-
rors is interinipted. An estimate shows that the gain cati be Increased in this case
Ical ",, Two variants of such a laser were tested (Fig. 1).
to almost/the theoret
Two Vby%ryWt&1s each 24 on 1mg aid 1. 25 cm In diameter were used. One crystal oper-
ated I-n-the Q-switching mode. The ends or the crystals mid the hypotenuse faces
of the total-reflection prisms were coated with ftF2 &M C&Fg fIl=O respective
The resonator comprised alternating dielectric coatings of CaF2 and ZnS (2 and T
layers) on plate glass and the prism. The plate was rotated at 120000 rpm. The
pump Illumination cam from two IPP-15000. and raw IYN9)00 j!!qLs and was Buff I-
Cord 1/3

L 31003-66
Ace xR: Ap6om8oi
Fig. 1. Diagram of laser resonator In Alch
the coupling between the active rod and both
reflectors is Interrupted. 1# 2 -- Ruby
crystalp Interm.1-reftection priamp
,4 -- plans-paranel glase put* with two
dielectric amtIngs.
4
cleat to cause losing without mirroze of one Mstalp by reflection from the free
ends# or else or two Metals with bleached ends. in tho case or a two-Dwer
coating on the semitransparent uIrrml, the vatrAD6nvW, was somewhat lwger than
5 j and 30% am than in the case of a free plAte, certain conditionsp an
energy of -U j was obtidned In variant a# as it re;uj ~of the toot that the reso-
Card 2/3
7
III, In

1; 310033-66
Acc mR: m6oo7fti
nator was Q-switched twice during the pumW pulse. 2te focused giant pulse pro-
duced breakdown in air. The laser pulse repetition frequency was 0.1 cps. Orig.
art. has: 1 figure and 1 formla. (021
80 CODIs 20/ OM DAM IOAt%65/ OM M 005/ OTH RM 002
ATD PRESS: q s
rd 313
C-0-
[

BODULINO VX., Prof.1 SHKLYAMMKAYA, Ys,Vo# kand. med, naukj YEROMHOLAN,
G.An student* -W~~
-- '=Lz
Toplical diagnosis of pulamary sebinococcosis. Uch sap, Stayr,
gost. mad. inst. M77-187 16.1 4MM 1727)
1. Xafedra obishchey khirurgli ( eav. - prof, VJ. Boduhn) Star-
rop)llakogo meditsinskogo inatituta ( roktar zaaluzhunnyy daya-
tell' nauki., Prof. V,Go Badylln)*

KOLPAKOV, L.G.; SAFRONOV, V.Ya.; LOPATIN, G.K.; FEDOROY, T.A.; r.RONEN, V.I.
,--
Possibility of usIng glandless puWs for pipelines. Trudy
heft' no-3:107-113 164. (MIRA 1R.-2)

SOCHILIK, R.G.; BLYUKMK. L.S.I_P~WTA. Ye.l.; AURCT. R.K.,
0 ill 0
red..; 0 TOA*~ -0
, t
Clisusitiou of Zeningrod onterWsos to a sh*rtor warMay]
Op3t perekhoda laningradakikk predprliatiL no isokrashchmnAyi
rabochii den'. Zeningrado Senisdatp 1960. 69 p. (KIRA 13:7)
(Seningrad-Mmrs of labor)

YEROITENKOV Ye L
-- -::,* 1--
Increacing the engineorIng atandardn, quality, reliability
and durability of manufactured articles. Bkt1.Lakh.-ekcn.
inform.Gos.nauch.-isol.inst.nauch.i tekh.inform. rio.6:62-
64 Ag 165. (MIRA 18:12)

PMQIMN;Rn-
takho
Cftt Is produotion cost) Cht t 50000isjoo~bl v~oduktfil.
0 OvO
Lanim,grad, Lanisdat, 1960. 41 p4
(Costs, Industrisl),

XALMTKOV, P.Te,; YZHDNIN. 7.2., LaiduWad
Physiological staMors of water consmWtion durtmg considerable
exposure to host. 71siol. sbur. 41 no.4:547-553 JI.-Ag ~ 155.
(WATUO WRA S.. 10)
requirommosi, off. of heat)
(HW, effects.
ou water roqmlrenonto)

MOM, 7.T.,, mayor medo'slubbr, kandensid,nauk
Improving conditions for working In protective (rabberived) clothing
In hot weather; Tosnq-pod~xhur.' no*'8#74-73 Ag 156 (XIU 1232)
(FRO""In dIMIX)
(NNAT-FgYSIOTMZOAX# Ir
I .

V.AWNIN,I, kand,med.nauk
11:7 ...............................
Water intake during work under high air tmap~rmturw and restoration
of body weight at different water rations. mod. zhur. Uzb. no.12:
41-43 D 161. (MIRA 15Q)
1. Is kafedry obahchey i voyennoy gigiyeny Voymmo-meditsinskoy
akad,emii imeni S.M.Kirova.
(DRIMUNG VAUR) (THIRST)
(BODY WEART)

YEHONINI N-4L.PO2kaVn'k-'
Weapons and tactics of t6 Platoon in the United States AM.
Starsh,-serezh. w.12:34 D 161. OML 15:3)
(United States--AnW)

#;aitrly Ivanovieb; TIMONIN, P.. redaktor; DANILIIIA, A., tekhnichooldy
rodalk.tor.
ttlnUnd; * polttleal and ocommic elmtob] flaltandlim; polittko-
ekon-micheskii otlwrk. Kooky&, Gov,lvd-ve politolit-ry, 1957*
215 ip - MU 10:7)
(linland)

15-57-7-10346
TrAnslation from: Referativnyy zhurnal, Geol0e;iYA, 1957, Nr 7,
p 250 (USSR)
AUTHORS: Snarskiy, A. N., Loginov, B. G., Yeronin, V. A.,
Shchelkachev, V. N.
TITLE: Results of Heat Application (Vystupleniya v preniyakh)
PERIODICAL: V sb: Metody uvelicheniya nefteotdachi plastov.
Moscow, Gostoptekhizdat, 1955, pp 107-113
ABSTRACT: Bibliographic entry
Card 1/1

- ......... ...... .-I......."", ....... ....... . .. ......... .. .............. -'-m I., " I.- I" - ~ "..I. ~ I - y u . , , ; I., P :;: I I I
- - - - - - - - --- --- - -- - -- - - - - -- - -- -- - --- - - - - -- - -- -- - --
YZRONIN, V.A.; MALITSIT, X.T.1 TAKRITOTj G.0o; SXYLTANOV,,S.A.
7--~NWO%ft ~
4Z= rntroducing now machinery and methods In the exploitation of
Tatar oil fields* Saft. Khos * 33,no.M24-31 0 ;i 1137. ~ (NM 11:1)
(Tatar AoSeS.R.-Petrolaux onginewins)

4~-N/93-58-7-7!17
AUMOR: G.G.; Y--r=i.=, V.A.; NO-1-1tosev. ~LV.; Malwrskiy, Y.P.
TITM: Pt~t:w~t', S+,eA w:d FLO-,me Devel%pmat of the RMIMSMI-: Oilfinlt~ i-..
Ibe Tat~ AM (Takoshcheye da'.I'-:,eysh--y raz;--aI,-Avki
matmzMemiya Tetarakcrr A39R)
PLPFaOVW-AL: W--fVjPzz:,-Je 1958,,,,Itr 7,,. PP- 324T 11IMS)
ABSMAM: T',-e ailfield of tba TWA-r ASOR use'-dItiowi-mrad in. ;Ia~y 1949.
A-5 th.Is fiOA the -Al cf vajmrcial valve is in the swr~ of the
DirL-, D--: D, ; W.A D-.5 ~.;be Mikbayiovakiy) Ii&v=-iaa fanwwas, as well as ia
tllvi f-,117-'~eaxtng sw;-as ;,f tbe earb=aceoas Voxwatica of :Uywer 03e D,
f,~r=1,61= is mie-; IuWrWev anA it hao'beez arbitrairtly w.,bdividei iat,-)
five 3ayprs: e-,-.a e. The 4 &-ad a 2&-~vra have b6tter jver.~silizjr &ad per-
waabili-1-7, azA Sraw~:,r oil capacity. Fig. 1 prtseatz #vi E"Ological pv:)fiel
nf the -. -) r
. R,-)mashkI: 11field, vhich is being davelAje-l acct~rdlzg to a VNII scbeme.
This scheme pr:;,vilss f,,r t2ae of reisarroir ppiesm". by we;.,-q c-f
-j
k-,jectiza ezA ttis makes it, p.--ssibls iv) artificia.317 ftputw:ot the cilfteld itto
23 mserv,:irs a:.,A tii expLoit -:lie five lAyers eof the D lormtlfv. J:-L*TWy- G,-::---
c-!A;T ftvn:.-. .:;t' the 23 restrvoira ara bmirz 4"r~wmi IIAL1.3p IOYP>i+AI-
Abdmkbm;3.,:-v-, Paylovukzqyu.
aad t~e Allmittl~v-v --:Ll reserviire
4-,:. Fig. 2. 7w AllmetIpv, A=Jmyevo., ea&aqp.I'm rilfieli aftit-
"Icme axe, k% (thpirp -,,f thc w3von -Al reservArti. %b2it ~. presex,s dat,% aa

]?xesent State and Fature Development of (cont.) Sov/9.3-58-7-7/17
vell spacing et the oilfield. The high operating presou M1 012. the injection
11z"As has made it, possible, to Increase the volum of vat.~r Injection (ref.1).
Shifts in tJi-. oil-bearing contows were determined by a 1!)57 TatN3:1 study using
isobar mps (Ref .2). M3e oil vield vas increased by fraelmtriua the formatioa
(IL-f-3). By A~Oril 1958 about 127 vells were being exploiled e'ither by EFN or
SM-5 Puns- !Me azilors make seven suggestions for the. Improve-ment, of the
Romashkiz.o oilrield ex 1P and Sovie
ploitation. There are 2 figares,, I tab 3 t
references.
Card 2/2 1. Petroleum--USSR

SAKU/60MO/005/002/002
A0,5VAOS
AUMOR: Yeroninp V,A.'-
Tl=i The Tartar Scientific Research Institute for Petroleum
PERIODICAL; Neftyanik, 1960, No. 5, pp. 2T - 28
TEMs A now method used in the Tartar RepublIc in oil drilling is the
maintenance of strita pressure by pumping water In-to prot6ising drilling levels.
The discovery of new oil fields was based.on research work-done by the All-Union
Scientific Research Institute of Petroleurd and Gas, (VNII); however, a local cen-
ter for promoting this woek inTw:tar SSR was considered rAO es"ry and has been g-- ow-
lng steadily since 1956, developing into a isciontific-teohnionl organization. Ear-
ly in 1960, as many as 200 specialists with higher educakton were employed at the
institute, 16 candidates of science and one professor. Ali many as 25 scientific
research laboratories have been organized, where 32 subj~ots were dealt with only
during 1959. The VNII was responsiblo for developing the first 6 drilling slte_~,
but the other projects numbering more than 15, were desIgned by the local In-qti-
tute of TatNII. New oil fields have been discovered on the territory ot Tartar Z~IZFR
in the last few years, and the institute has already prospared plans for thelr de-
velopment. 'Special attention is devoted by the institute to the problem of further
Card 1/3

S/ (R2166100010051002-100 2
AO,5'1/AO26
The Tartar Soifintific Research Institute for Petroleum
study of the Romashkinakiy oil fields, introducing new p?4ssure wells, the hydro-
-explosion of utrata, and maximum oil yield from the strata undeer conclitions of
contour and internal-contour water pumping. The department far drilling laborato-
ries has complooted research work on the following subjeate: 1mreasing -the effec-
tiveness of thii fight agaiKist absorption of irrigating 1:1,quids under corsdItions
encountered In the Homashkinskiy oil depositel the aomp~)oltian and techniquq of
preparing high-viscose plugging liquids, It was recommended that local materl.fds 1;A_
used as inert fillers for plugging cements. Suggestions viere made for improving
the prospecting of promising strata and cementing of casing colimm under cor4lti7n
enccuntered In Tartar SSR. Asummary of experiences was madle of dfl1ling oil.-wells,
having a smaller diameter. The laboratories ot the oil fteld dopartment are f3tiidy-
Ing working parameters of the gusher elevator, they are ,inproving the flatit,
paraffin deposits, they are working on analysis and lmpvrnremert of a:~-~!~e d-enT~~1-
sifying apparatus, on testing new types of de-emulsifiers.. A number of deB.-gr.5
fi4ve been drawn up for simultaneous individual oil aelontlon und that of water in
tAe well, located in the water-oil zone. Several instrumertB witt, local a";Ilomatlorl
have been produced, the designing of a bellows-sealed aut'.omatic relay. tested in this
Card Z/3

SAY9216010001005100 P
AO5.1/AO26
The Tartar Scientific Research Institute for Petroleum
oil field, has been completed to be used for pumping proc~,&Ires, using limited-
-level transmitters; an instrument for recording the dellyVation of oil, dmring
the movement of the liquid along the pipes; a connumption-meteti, for determinirg
the acceptability of each stratum, especially when water Is pumped Into the pres-
sure wells; tesperature-determining device in an active gusher well, based on elec-
tronics and semiconductors. In 1959,departments for oil k,*fining and gas were
established, participating in the formation of a Tartar oil-refInIng base. The In-
stitute is said -to be located directly on the site of the oil wells, thus facill
tating productian and attracting oil specialists to scientific research work. V
Card 3/3