SCIENTIFIC ABSTRACT VOROBYEVA, E.I. - VOROBYEVA, L.A.
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SCIENTIFIC ABSTRACT
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am4LOBRUCHEVO D.Y., doktor biolog. nauk,,
.NIKITINAP O.G., redoizd-"; BA=p A#I~j
~~~KOVA# O.M., takhn, red,
(Rhizodontid crossopterygians in the main Davonian field of
theIU.S.S.R.] Rizodontnya kisteperys ryby Glavnogo devonakogo
polia SSSR. Moskva, Izd-,vo Akad. nauk SSSR#-1962. 137 po
(Akademiia nauk SSSR. Paleontologicheakii institut. Trud
94). Us
o* (MIRA :L6r 6
n
(Rhizodontidas)
SLAVNYY, Yu.A.; VOROBIYEVAO B.S.
Deposition of silica from soil solutions during freezing
Pochvovedenia no.9:80-84 8 062. jMIRA 16:1)
1. Pochvennyy institut imeni V.V.Dokuchayeva.
(Amur Valley-~-Solls-Silicon content)
(Zeya Valley-Soils-Silicon content)
(Frozen ground)
.......... ~ --11- - - - -- .,- ~
bk9j,j3, yr-t, Id pr. --/-,
AIZKSANMOVA, IvudmilA Nikolayevna; WAYDENOVA, Ollga Aleksandrovna;
VOROBOYEVA, F.I., ad.; CHUNAYEVA, Z.V., tekhn.red.
%ftwwmm~ -
(Practical laboratory exDeriments in soil science] Laboratorno-
prakticheskie zaniatiia po pochvovedeniiu. Mockva, Gos. izd-vo
sellkhoz.lit-ry, 1957. 214 -p. (MIRA 11:1)
(Soils--Analysis)
VOROBIYEVA, F. M.
"The Variability of Biological, 11!orphological, and Noononic
Characteristics of Wheat After Its Conversion From Winter to
Vernalized Forms." Cand Biol Sci, All-Union Inst of Plant Growing,
VASKhNIL, Leningrad, 1953. (RZhBiol, No 1, SeP 54)
SO: Stua 4321 21) liar 55
In.
SIOZATA, YO, Fo, prof.,doktor biolo I i~l'skokhosy*ystrswqkh asuk;
VOROBITIVA, F.K., keaL biol. nauk; POGCRWSKTI', B.X., kand. biol. nauk
Studying the Interrelationship of growth and development In higher
plants, Trudy po prikle bot., gens I eel, 30 no, 3173-124 137,
(HIRA 1117)
(Growth(Plants))
USSR/Plant Physiology Growth and Devolopzento I*
Abs Jour : nor Zhur Biol., No '213", 1950, 104399
.1
Author : Ginslmya) YcoN.) Voroo rletskayn, D.K.
List : .
Title : Exploring the Interrelatiollullip of Growth caid Davclojr.,mt.
in IML4ier FlantGo
Orig Pub : Tr. po Pro Botqno Gone-'%,.. i solaktsii) 30) No 3) 75-124;
1957-
Abstract Plants of various spec~cs were Cxown for various periods
of time under individually suitable photoperiodic condi-
tions (long-day picaits on natural day in the stvizior
various regions of the Buro-pean part of the USM, cad
short-day ones, on 8-hour day), ithercupon the lon-day
U
plants vere exposed to t;hort days (from 9 to 12 hovx* i-Or
differa:it species)) and ",-lic short-day plants) to na-Zural
day on their natural plantin,...- sites (towns of PushIld 'n aad
Miibiny for horehound; av.CL Mimsaodar for sesame). For the
Card 1/3
USSR/Pldnt Phy'sioloGy - Growth and Development-*
Abs Jour nof Zh .ur Biol'.~ ~o 23, 19501 1011399
.early-ripening and nornal-ripr-ming varieties of fl-,:,,
lallemantia, oil, milIcviccd, spring rapc~ Elscholtia cr--s-
Lata,wheat- (Krasnodar!= Varict-y) and barley 3 ;-rariciIZS),
the period.of the corincrIcement of the stage of maximal
Growth changed with nchan~~ in the photoperiodic ncCc,
as compared with control plants; in the author's opiuf.011)
this period MY. serve. as an Lidlicator of the termination
of the light-exposure sk'aGe. For the late-ripening, varic-
tics,or flax) Dracoccphal,= moldavicum, spring false flax,
an(! -sesame, the period. c~f ~~th7q~~ conmencement- of the sta,-c of
dmal. growth did notchango Upon a change in the day
~icngth, and it can not-,rorve as an indicator oi~ staGe dcve-
lopment. P.Lants of thc--
.L)crilla both those nonvernalized
aad those vernalized Li darlaictss or in light) werca [Xown
for various periods of 10-hour days and subsequently c,.-po-
sed to natural or aontinuous clay. In the plants [;L7oini for
9 to 15 10-hour days there appeared sprouting forms.
Card 2/3
Namet VOROBIYEVA, G. A.
Dissertation: Stulieo on ajrntheeis In the field of alicyclic terpene,
compounds
Degree; Cand Chem Sci
Min Higher Education USSR, Moscow Inst of Fine Chemical
Technology imeni M. V. Lcmonosov, Chair of Technology
of Drugs and Scents
Date se =-e) Place: 1956, Moscow
Source: Knizhnaya Letopis', No 2~ 1957
Ycl~~ i I.K.;VOROBIYEVA, G.A.; MOBRAZHENSKIT, N.A.
Rev method of synthesizing the asters of polyanocarbonic acids.
Part*7. Zhur.ob.khim. 27 noolO:2653-2662 0 157. (MIRA 11W
1.1natitut tonkoy khimicheeko3r takhnologii.
(carbonic acid) Ocetera) (Unsaturated compounds)
YE-t /-,4 6:
SARYCHIVA, I.K.; VOROBIYEVAp G*A.; MOBUZHEI=IY. N.A.
S7ntheals of 2,3,6-trimethylundecatrion-206,8- one-10 (peaudoirone).
Part 2. Zhur.ob.khlm. 27 no.iO:2662-2667 0 '57. (MIRA 11:4)
l.Institut tonkoy khimicheekoy tekhnologli.
(Peaudoirone)
VO %1' 6-
79-11-17/56
AUT11ORSt Sarychevaq I. K. 9 Voro4feva, G. A, t Kucberyavenko, L. G.
Proobrazhenakiy,
TITLEj Synthesis of 2,3,6-,2ritiothyloctadione-2,7-olo-6-3-i-,Ictliy1 Linalool
(Sintez 2o3,6-trinetiloktadiyen-2,7-ola-6-3-1~ictillilialoola)
PERIODICAL: Zhurnal Obahchey Khimii, 1957t Vol. 27, Ur 11, pp.2994-2959 (USSR)
ABSTRACTt In the described methods of synthesis of the ironO3 1-brumo-2,3-di-
methylbutene-2 and 2,3-diuethylheptene-2-on-6, which are over 3-
-methyllinalool and 3-mothylcitral converted to poeudoirones, re-
gularly occur as intermediate products. '2he replacement of 2,3-di-
methyllieptene-2-on-6 by 2-methyl-3-methylenehep'lanone-6 caused no
essential chan-es in theschemes recommended earlier and only de-
cided the question concerning new 3ources o~ raw uatcrial. Y'herc-
fore it Yras of interest to work out, on the b_--ji.: of the acOO33ible
a new way for the structural groupink; 11~ 11.3
CH I ~ - CH
which represents a otartin'-point of quite a nuviber of inter-nedia?e
products in the ironc synthoai3. The pr,::_,.,i:t the
uynllhosis of 3-110thyllinalool., itarting fro;:i th6 nethyl acetoacetic
aste r: This cater is converted to 3-:;letli~,11),nt.,aic)ne-4-01-1, t*iis
Card 1/2 is a,-ain transformcd to 2,3-3imethylpc~ntadiol-2,5 which is con-
Synthesis of 79-11-17/56
2,396-2ri7icthyloctadiQne-2,7-olu-6-3-~lctlyI Linalool
vertod to 2-5-dibrorio-2)3-dil:latl,YlPutit~tile cnd ftirthcr to 5-bru,.io-
2,3-dinothylp,entene-2. By conden3ation with Lx thylvinylkatone in
the presence of lithium the firal product -,-ias converted to 3-.-,I--th--
yllinalool with a 14,1 ~o Iiiold (3ce schLime 1). Thuo the sjnthesi3
of 3-nothyllinalool was realized over quite a number of inter-
mediate products. ITC-0 Methods of the iyrithe3ia of 1-bro:lo-2,3-
-dimethylbutene-2 and 20-dimethylhoptone-2-on-6 were worked out.
'2here are I fi:,ure, and 6 references, 1 of which is Sla4c.
AS~JOCIATIOIlt Moscow Mistitute of Fine Cbemical Tlechnology
(1.1oskovskiy institut tonkoy khinicheakoy tokhnolo-ii)
SUMITTED: October 8, 1956
AVAILABLE: Library of Congresi
1. Irone synthesis 2. 2,3,6-TrimettWloctadiene-2
7-ols-6-3-Mett71
,
linalool-Synthesis
Card 2/2
AUTHORS:
TITLEs
PE140DICALs
ABSTRAM
Card 113
Sarycheva, 1. 2[, , VoroYXe-t a G, A,
i 79-28
Kuzn~-tsova, 11. A,-;-Ffeo r-nz A-
A New Synthesis of the 2,6i!0,14-Tetramethylhexadecene-
-15-ols-14 of Isophytene (Irovyy sintez 2.,6,10,14-
tetrametilgeksadetson-15~ola-14, izofitola)
Zhurnal Obshchey Khimil,.1958, Vol, 28, Nr 3, pp. 647-651
(USSR)
The method of synthesio,of the vitamins E (tokoferolov)
and Vitamine K, k-fi2lokhincria) which have been published
until now are based on the utilization of the 2,6,10.14-
tetramethyl.hexadecene.-14--ols.-16, called phytene, wh-4.-.h is
only produced of chlorophyll, one kilogram from one ton
of chlorophyll (Ref 1) (see the respective reaction process).
The known semisyntheses (Ref 2) are based on the utiliza"Cion
of natural tarpene- and.seequiterpene aloohols of the
aliphatic series and until now havo not found oonsiderable
application. A,,1cording to the inve8tigations of vitamins
3 and K, as well as of other natural produc"a It, was found
that the nompound isomerio t3 phytene, namely 2,1.6,10,14-
A New Synthesis of the 2,6,10,14-Tetramethylltexadecene- 79-28.3-118/61
-15-018-14 of Isophytene
T,
tet~rameth,ylhexadecene-15~-01~-14, he ~s,,~phytene (formula
VII) fully substitutes phytene, (Ref 3). (See reaction
process 2 with formula VII 1),-1n the present work a
new complete synthesis of isophytene (VII) is realized
(see formulae I,II,III,IVV.i ard VI); as basic; material
~~6--dimethylundeqadi-.ene.-2,,.6--on..":O and geranAlacetone (II)
is used which -Ls prod-aced of synThe.cic. Iinaloa (I.)..
either by means of the diketene of the carxesponding
acetoacetate, or by a reaction using the aoetoacetate with-
.~put the separat-ion of the aoetoacetate (II).. The 2,6-di-
jaethy,lundekadienG-2,6--on-10 (II) converts t.) 2,6,10-
trimdthyl.dodakadiene.-2,6-in.-I!--ol-lo by the ption of
sodiumacetylenide in liquid ammonia,, The former is tha
deh~lronerolodene (III) which then reacte with acetoacetate.
In this case, different from the known syntheses of phytene
and isophyteno (VII)., the necessary elon...gation of the
carbon chain up +.o C18 is reached In one step, The 2 '.6,10-
trimethylpontadekatetraene-,2.,6,.10,12..on-.14 (VI) synthetized
this way -is hydrated in the presence of a nimkel catalyst
Card 2/3 and ionverte to the 2,6,410-trimeth,,rlpentadekAnol-.1.4. The
A Ifew Svnthesis of the 2,6,10,14-Tetramethylbezadecene- 79-23 3-18161
-15-ols-14 of 1sophytene
latter 4a oxidized with a chromium mixture,in acetic Acid
to 2,6,10-trimethylpentadekanone-44 (V), Furthermore the
condensation (Y) with sodiamacetylendien---~',realized; the
obtained 2,6,10,14-tatramethjlhexadecine--15-o--"4 (VI)
finally converts to isophytene (VII) by "selective hydra-
tion" in the presence of the Lindlar catalyst (Ref 6).
There are6 references, 2 of which are Soviet.
ASSOCIATIO14: Moskovik-1-y.institut tonkoy khimicheakoy tekhnologii
(Moscow Institute for Chemical Precision Teeb-nology)
SUBMITTEDt March 14, 1957
Card 3/3
KRUGI,TKW, S.S.; KUDRYOTSEV, NJ,; VOROBIYEVA, G.F,
. w--~
Mothod of determiLing the concentration of levellng adMItIves -In
eolutions for the electrolytic application of rptallic coatinga.
Zushchomet, 1 no#0439-441 JI-Ag 165o (VJRA IM)
1. Wskovakiy khImIkG-tekhnologichssUiy inatitut Irrert rj,,I,
Wndfileyeva.
KONDILENKOp IJ.; VOROBIYEVA, O.A.
Annular low-pressure mercury lamp. Prib. i tekh. ekepo 6 no*2:
142-145 Mr-Ap 61. (MIRA 14:9)
1. liyevskiy gosudarstvennyy universitet.
(Electric lighting, Mercury vapor)
5 W-
.41UTHdRS: Voroblyevap G. A., Sarychova, I* K#p BOV/75-29-7-46/83
__T F-M-7
feo razh71Mkt7y A.
TITLE: Synthesis of 2t6olOtl4tl8p22-Hexamethyltetracosahexaen--
2j6,10214918,23-01-22, the Farnesylnerolidol (Sintez
2,6,10,14,18,22-1;oksametiltetrakozageksayen-2,6,10,14,18,23-
ola-22 farnazilnerolidola)
PERIODICAL: Zhurnal obshchey khimiij 1959, Vol 299 Nr 7, pp 2314 - 2318
(USSR)
ABSTRACT: Farnesylfarnesol C a component of the natural P-phyllo-
30500'
quinone (vitamin K 2) (Ref 1), belongs to the group of isoprene
polymers'oocurring in nature, such as rubber, gutta-percha,
solaneso *1 (C5OH800), and other polyterpenes. The physico-chem-
ical and biological properties of these compounds are connected
with their stereo-isomerism, caused by the presence of double
bonds and methyl groups. The cis-trans isomerism complicates
the synthesis of similar isoprenoid compounds, as conversions
of the spatial configuration in the course of a reaction lead-
Card 1/3 ing to mixtures of the isomers 'have frequently been observed.
Synth'asin of 2l6llOil4,113f22-flexamothyltatracoca- 807/79-29-7-46/83
hexacn,:-.2t6plOP14tlBP23-01-22I the Farnesylnorolidol
In the present paper the synthesis of farnesylnerolidol (I) by
condensation of Pq-unsaturated alcohols with acotoacetio es-
ter (Ref 3) is described. Norolidol (II) (Ref 4) is used as an
initial substance. The stepwise building up of the isopreno
links of farnesylnerolidol (I) was effected by the application
of three similar methods, which included the synthesis of the
ketones by means of acetoacetic ester or acetylacetone, con-
densation with acetylene, and selective hydrogenation (Scheme
Compound (II) interacted with acetoacetic ester to yield (III~,-
(III) being converted to (IV) by condensation with sodium
acetylide. Pd-catalyzed selective' hydrogenation of (IV) gave
(V). This alcohol (T) was then submitted to a similar reaction
cycle. Thus, the compounds (VI), (VII), and (VIII) were obtain-
ed successively. Farnesylnerolidol was finally synthesized from
(VIII) by way of the intermediates (IX) and (X). There are 5
references, I of which is Solviet.
Card 2/3
Synthesis of 2,6110,14,16,22-Ilexamethyltatracosa- SOV/79-29-7-46/83
hixaen.~-2,6,10,14,.18,23-01-22, the Parnesylnerolidol
ASSOCIATION: Moskovskiy institut tonkoy khimicheskoy tekhnologii imeni
M. V. Lomonosova, (Moscow institute for Fine Chemical Technology
imeni M. V. Lomonosov)
SUBMITTED; March 27) 1958
Card 3/3
50)
AUTHORS: Sarycheva, I.-K., Molotkovskiy, Yu. G., SOV/79-29-4-16/77
Vorobjeva, G. A., Preobrazhenskiy, N. A.
TITLEs Complete Synthesis of 2-Methyl-3-phvtyl-naphthoTjjnme-1 4
Vitamin K, (Polnyy sintez 2-metil-3-fitilnaftokhinona-1,4-
vitamins, Kj)
PERIODICAL Zhurnal obahchey khimiij 1959, Vol 29p Hr 41 pp 1123-1126
(USSR)
ABSTRAM In the present paper the synthesis of vitamin KJ(I) is
,described which is based on the condensation of
2-vieth.vl-naphtho-hydroquinone-1,4 (II) with isophytol (M)
in the resence of the ether compound of trifluoborate
(Schems~ (Ref 7). The initial product for (III),was the
pseudo-ionone (IV) (Ref 8). The pseudo-ionone is hydrogenated
in the autoclave in the presence of the nickel catalyst to
give compound (Y) which is directly oxidized with the
chromium mixture to (VI) without any separation. Compound
(VI) is transformed with sodium acetylenide into (VII)
which is converted by acetoacetic aster first into (VIII)
Card 1/2 and then via (IX) into-(X). The condensation of (X) taken
Complete Synthesis of 2-gothYl-3-PhYtYl-naphtho quinone-1A SOV/79-29-4-16/77
Vitamin Ki
place with sodium acetylenide with (XI) being formed. (XI)
is reduced in the presence of the palladium catalyst to
give isophytol (III). It must be mentioned that the
physico-chemical constants of isophytol which was synthesized
from linalobl (Ref 11) were somewhat different from the
given sample, obviously owing to the predominance of various
diastereoisomeric forma in them. The product of the reaction
of isophytol (III) with 2-mothyl-naphthohydroquinone-1,4 (II)
is the 2-methyl-3-phytyl-naphthohydroquinone-1,4 (XII). This
is oxidized to give the end product (I), the vitamin K,. The
vitamin K, synthesized by the authors corresponds with the
natural one as far as its properties are ooncernedl this
was confirmed by the spectroscopic investigation (Fig).
There are 1 figure and 13 references, 5 of which are Soviet.
ASSOCIATIONt Moskovskiy inatitut tonkoy khimichaskoy tekhnologii
(Moscow Institute of Fine Chemical Technology)
SUBMITTED: 'March 4, 1958
Card 2/2
-5 (3)
AUTHORSt Sarycheval Ia Kot Shuntoroviohl Ye. If-p SOV/79-29-4-32/77
Voroblyevay G. A., Proobrazhonskiy. If. A.
TITLE: Synthesis of the 7-qyano-296-Dimethylt anh 2,326-Trimethyl-
Heptadienes-2 16 of the Nitriles of the Geranic and 3-Methyl
G'eMnio Aoids (Sintez 7-taiano-2p6-dimetil- i 2,'3#6-trimetil-
gaptadiyonov-2,69 nitrilov gortniyevoy i 3.M(j~ilgeraniyovoy
-PERIODICAL: Zhurnal obspchey khimii, 19599 Vol 29, Nr 4t pp 1189-1192
(USSR)
ABSTRACT: In.the terpene series the synthesis of the nitrogenous
compounds is of importance since they (e. g. amines and nitriles
render possible the synthesis of geraniol, citral, geranic
acid and numerous homologues (Ref 1). The present article
contains a description of the synthesis of the nitriles of
geranic acid (I,R=H) and 3-methYl geranic acid: (IfR-CH 3)
starting from 2 -methylheptene-2-on-6 (IV,R- H ) andt
accordingly, from 2,3-dimethyllieptene-2-on-6 (ITR&CH 3)
Cara 1/3 (Pattern 1). Compound (IV,R=H) is synthesized as initial
Synthesis of the 7-Cyano-2,6-Dimethyl, and SOV/79-29-4-32/77
293p6-Trimethyl Hoptadienes-2,6 of the Hitriles of the Geranic and 3-MethYl
Geranic Acids
product from (119R-H). This alcohol is transformed (Ref 2)
into the bromide (iir,RnH) which is condensed by acetic
anhydride (Ref 3) in the presence of magnesium. In order to
artive at (I,R-H), (IV,R-H) is transformed with oyanoacetio
deid. Compound (I,R-H) is also obtained by transformAtion of
kIV) with ethyl cyanoacetate and subsequent selective
shponification and decarboxylation of the compound (V, R-H)
o'btained. Similarly, the synthesis of the nitrile of the
compound (I,R-CH3).'s carried out, namely by the transformation
of (IVPR-CR 3) with the ethyl cyanoacetate. The structure of
the initial product (I) was provediaocording to pattern 2.
The divergency found between the physicochemical constants of
the synthetid nitrile of.geranic acid (ItR.H) and thbee of
the nitrile prepared from natural citral (IX) (Ref 6) is
explained by the differences in-the relative sterecLsomer
contents (Ref 7) (last pattern). There are 7 references,
4 of which are Soviet.
Card 2/3 1
.S$nthesis of the 7-Cyano-2,6-Dimethyl# and BOY/79-29-4-32/77
2,3,6-Trimethyl Heptadienes-2,6 of the Nitriles of the Geranio and 3-methyl
Geranic Acids
ASSOCIATIONt Mookovskiy institut tonkoy khimicheskoy takhnologii
~(Moscow Institute of Fine Chemical Technology)
SUBMITTED: March 31, 1958
Card 3/3
KONDILENKO, I.I. k~2 OBITIVA, G.A.
innalar low pressure mercury lamp. Opt.1 spektr, 9 no.4:524-525
o 16o. (MIU 13:11)
(Electric lighting, Kercury vapor)
VGHOBlYEVAq G.D.
Riperimental data on the course of wounds in radiation sickness.
Eksperakhir.i anest. no*6t46-48 161* (MIRA 15:5)
1~ Iz kafedry gospitallnoy khirurgii (zav. - prof. A.M. EVkhtso
(deceased]) Krasnoyarskogo meditoinakogo instituta (dir. -
doteent, P,G. Podzolkov),,
(RADIATION SIMESS) (WOUNDS)
Wi~MIYZVA, G.D.
~ I -
remale genitalia In a hernial sac in a boy, Pedistriia 36.no.6:9o
Je' 158 (MIRA litO
1. Is goopitalinoy khirargichaskoy kliniki Krasnoynrakogo maditsinskogo
institutas
(HERNIA)
ROZOVSKIY N*V*
.9 , p r o f . ; ~Y~B 1 M. Ci,_Df- - I
Therapy of cardinspasm. alrurgiia 40 no.1:71-73 Ja 164.
(MIRA 17:1:)
1. Kafedra gospi.tallnoy khirurgli (zav. - prof. N.V. Rozovskiy)
Krasnoyarskogo meditsinskogo instituta.
TOROBITIVA. G.7.1 ILYUSERMO, V.M.
Separation of antimony.*and indium by the anodic oxidation of mixed
amalgams, Izv.AN Kazakh.SSR.Ser.khim. no,1:39-43~ '59. (MIRA 13:6)
(Indium-Ifercury alloys--Analysis)
(Antimony-Mercury alloys--Analysis)
KRUOLIKOV, S.S*; DUDRYAVTSEV, LIVOVSKIYJ V.M.
Investigating electrolytes for surface-leveling nickel plating.
Zhur.prikl'.khim. 33 no.4s781-786 Ap 62. (MIRA 15:4)
(Nickel plating),
9RUGLIXOVt S.S.; KVDRYAVTSEVj N.T.; VOROBIYEVAj G.F,; L'VOVSKIYj V.M.
Effect of ripple current on surface leveling in nickel plating,
Dokl. AU SSSR 140 no.4:877-879 0 161. (MIRA 14:9)
I,Moskovskiy khimiko-tpkhnologicheskiy institut im. D.I.Mendeleyeva.
Predstavleno akademikon A II.Frumkinym
6ickel plating)
I**
XUDRYAVTSEV,~*,N.Tj, prof.1 KRUGLIKOV; B.S... kand, khim. nauk;
VMBIYEVA, G.F., kand. Irbimicb. nauk
.-I .-I-~ I.
Eleeimi,ytie metal plating with the leveling of the surface
I of articles. Zhur. VKHO 8 no-5:493-501 163. (MIRA 171l)
VORO,Ylrv~ 6~:F_
XUDRYAVTSEV# NeTe; KRUGLIKOV, SaSe~, ~F#j ZUPOVj M,,S*
Surface-leveling action of some nitrogen-containing heterocyclic
compounds. Zhur.prikl.khim. 35 ne.4: M-781 Ap 162.
(MIRA 15:4) *
(Heterocyclic compounds) (Electroplating)
AUTHORS:
TITLE:
PERIODICAL;
" ~~" -j ~ 1:
S/080/62/035/004/008/022
D202/D301
Kudryatsev, N. T., Kruglikov, S. A., Voroblyeva, G.
and Zubov, M. S.
it study of the smoothing effect of some nitrogen-con-
taining heterocyclic compounds
Zhurnal prikladnoy kiiini-J, v. 35, no. 4, 1962, 777-781
TEXT: The 'authors tested quinoline, methyl-quiriolinium iodide,
quinaldine and acriflavin as smoothing agents in nickel electro-
plating aiid urorked out optimal conditions for their use. In their
opinion only quinaldino may be of practical use, becauoe quinoline
and its -methlodide havc compnratively amall i3moothing effectc and
L-ive brittle deposits. Acriflavin producea it favorable offect but
only in a very narrow concentration range, which mukea It un8uitablo
for practical purposes. An addition of saccharin to electroly-tes
containing quinoline or its derivative gives a less brittle plate,
but markedly lessens the smoothing effect of these compoandO. Ex-
perimental details and.the obtained.re,culto are given. There are
Card 1/2 : I . X
S/080/62/035/C'v'4/00VQ22
A study of the ... D202/D301
5 figures, 1 table and 13 references: 3 Soviet-bloc and 10 non-So-
viet-bloc. The 4 most recont, references to the English-language pu-
blications read as followo: S. A. Watoon and J. E. Edwardj, Tranu.
Inst. Metal Pinish, 34, 167, 222, 1957; E4 Raub, Plating, 46, 486,
1958; S. E. Beacom and B. J. Riley, Metal Ind., 95, 103, 1959; S. E.
Beacom and B. J. Rileym J. Electrochem. Soc., 106, 309, 1959-
SUBMITTEP: March 27, 1961
PWOUKOV.p S-S.1- KUDRrAVTSEVj N.T.; VDHDBMII O.F.1 AMSOV, A.I.
wOn the Mechanism of the Action of LevelUng Agents in the
Electrodeposition of Metals.*
Report presented at the 14th meeting GITC19p Intl, Com, of
Blectrocbendcal Thermodynamics and Kinatiiss, Mbseow,, 19-25
Aug 63o
YAndelsev Chomico-Technological Institute, Moscow, U.S.S.R.
S/080/62/035/004/009/022
f, lit D202/D301
AUTHORS: Kruglikov, S. S., Kadryatoev, N. T., Voroblyr;vla., G., P.
and blvovakiy, V. 14.
TITLE: Investigating electrolytes for umoo-th nickel plating
PERIODICAL: Zhurnal prikladnoy khimii, V. 35, no. 4, 1962, 781-786
TEXT: The aim of this study was to check, the hypothesis of Western
investigators: Watson, Edwards, Foulke and Yardos, concerning the
mechanism of the action of smoothing agents in nickel electroplat-
ing. The present authors used a pulsating d.c. and coumarine and
quinaldine as smoothing agents, these compounds being added to the
electrolyte separately or in mixture. The results proved that iln
the smoothing process the relative speed of diffusion of the agent
to various parts of -the cathode is the decisive factor. The addi-
tion of coumarine is most effective between 20 - 3000; when an ex-
cess of this compound is used the electrolyte becomes self-regulat-
ing, as' the ooumarine solution remains saturated dvring the whole
plating process. The addition of a mixture of the above compoundu
Card''1/2
3/080/62//03 5/004/009/02 2
Investigating electrolytes -Lor ... D202/fD301
is recommended, an even nickc~l plate being obtained in a -wider
range of conditions, and much more compact than v.,ith single
Experimental details and results are g'lven. There arc 5 figuresp
2 tables and 7 references: 4 Soviet-bloc and 3 non-Soviet-bloc. The
references to the English-language publications reLd as follo,.-Is-
S. A. Watson and I.Edwards, Trans. Metal Finish, 34, 222, 1-957; D.
G. Foulke and 0. Kardos, Proc. Am. Electroplater's Soc., 43, 172,
1965; 0. Kardos, Proc. Am. Electroplatuer'8 Soc., 43, 181, 19506.
SUBIMITTED: March 27, 1961
Card 2/2
KRUGLIKOV,'S.S.; jO%QA'TEVA,.jG.F.; KUDRYAVTSEV, X.T.; YARLYKWtM-M-;
P
ANTONOV, A.Ta.
Mechanism of surface leveling in the electrodeposition of metals.
Dokl. AN SSSR 3.49 no.4:911-914 Ap 16~. (KcRA 16:3)
1. Moskovskiy khimiko-tekhnolojicheskiy institut im. D.I.Mandeloyeva.
Predstavleno akademikom A.N,Frumkinvm,
(Flectroplatipg)
AUTHORS: Karelinj Ya-A- and Voroblyeval G.I. 65-lo-6/13
ication ffluent Waters from Refineries
TITIE: Biochemical Purif Of rer--
(Biokhimicheskaya ochistka stochnykh vod neftepe
abatyvayushchikh zavodov)
PERIODICAL: Khimiya i Tekhnologiya Topliva i masel,_1957, ITO 10$
pp. 29 34 (USSR~
ABSTRACT: Laboratory investigations on the possibility of the
application of bacteriological purification of refinery
effluents are chscribed. It was established that Pseudomonas
bacteria actively decompose crude oil and individual hydro-
carbons. Of the cultures separated, the most active were:
Pseudomonas Putida Flugge, 1886; Pseudomonas Dacunhae (Gray
and Thornton, 1928) and an undetermined type which was called
Pseudomonas species. There are 2 figures, 6 tables and 5
references, I of which is Russian and 4 English.
ASSOCIATION: MISI imeni V.V. Kuybysheva
AVAILABIE: Library of Congress
Card 1/1
USM/MicrobioloEW - General Microbiology, r-1
Abs Jour : Ref Zhue- Biol.., No 12, 1958, 52(26
Author : Voroblyeva, G.I.
Inst AS USSR
Title A Study of the Role of Bacteria of the Psoudomonas Type
in Petroleum Microbiology.
Orig Pub Dokl. All SSSR, 1957., 112, 116 4, 763-765
Abstract From samples of petroleum and water occurring below the
petroleum layer collected from a depth of more than 1000
m in different petroleum-bearing.regions of the Kuybyshev
diGtrict~ fluorescent microorganiems were isolated rescm-
bling the folloving species of the genus Pseudomonas:
P. acroginosa, P, dacumhae) P, fluoreeceno, P. putida, P.
arvilla, These bacteria are facultative anacrobes and can
act under aerobic as well as anaerobic conditions.
Card 1/2
USSR/Microbiolo(g - General Microbiologys F-1
Abs Jour Ref Zhur - Biolo, No 12, 1958, 52726
The same culture can act on various hydrocarbons, while
the absorption of 02 in the presence of glucose is lcxcr
(2.8.10-i-L ml per hour per cell) than in the presence of
docane (22.2.10-11 ml per hour per call). All the cultures
actively develop in the presence of 1-8% NaCl in the madium,
but can withstand con3iderably stronger concentrations of
this oalt (15%). Thu wide distribution of microorganisms
of the genus Pseudomonas in oil wells,, and their ability to
develop on petroleum under anaerobic conditions, allow the
ascumption that they are part of the biocenosis of oil
fields. -- G.I. Vomblyevn
Card 2/2
- 12 -
-7 -?
t ~4'x- ex-
4/1 r Blol Sci
EROB G 6~ VA a e (dies) -- "A stuay of microorganisms of the
~~~ 7
genus Pseudomonas isolated from oil deposits". Moaccw, 195n. 15 pp (Inut of
Microbiolo6f Acad Sci USSR), 130 coplea (KL, I-To 1, 1959, 117)
FISHER, P.N.; KEYLO, I.A.1 VOMBI.YEVA G.I.; SHVARS)UfNp BAI ALYANDVSKATA,,
A.T.; SHILOV,*Yu.P.
T.S.; ZYBIN,
-Growing Mast on hydrolypates from coniferous vood. Gidroliz.
i lesoWm. prom. 16 no.5t7-12 163. (MIRA 17:2)
1. Mookovskoye otdeleniye Gosudarstvannogo nauchno-iseledovatell-
skogo Institute, gidroliznoy i oullfitno-spirtovoy promyshlennosti
(for Fisher, Keyll. VorgIL!M.41 Shvartakroyh, Alyamovskaya).
2. Ivdellskiy gidroliinyy zavod (for Zybin,, Druzhininap Shilov).
OW"ol'4
"UA
KRYUCHKOVA, A.P.;-YOR~I~q~
j.!~ 1. "'
.Respiration of fodder yeasts and the accumulation of their
biomass using various carbon sourceb. Mikrobiologlia 32 no.5t
856-862 S-0163 Off RX 17 %2)
1. Gosudarstirennyy na-ucbno-Issledovatel'skiy institut gidroliz-
noy i oulifitno-spirtovoy prom-,mhlennosti, Moskovakoys otdole-
niye.
KRTUCHKOVAv A.Pij_y~ljlqj~'YEVAp Mel KIM', 1. !A4
Effeat of carbon source in tha medlum on a-m-lno acid a.-ynthesis by
yeasts. llrikl. biokh" i rdkrobiol. I no.D78-82 Ja-F 165.
(MIRA 18:5)
1. Vsesoyuznyy nauchno-issledovatellskiy institut blosinteza
belko,,rfkh voshch-3stvp 1-1,oskva.
RODIONOVA, G.S10; Y~ROBITSVA,~G.--,~; KRYUCHROVAx AP.; STEPAWIMOp V#G.
Yeast adf-Dtatlon to furfurole. Gidroliz. i lesokhim. 18 no.2:3-5
165o (MIRA 18:5)
1, Vsesoraznyy naucbnO--ssledovatellskl.y institut biosinteza
belkovykb. vesbohostv.
KRYUCHKOVA, A.P,; VOROBIYEVA,,- G,I.
Order of assimilation of hexoses and pentoses b7 yeasts. flidroliz.
i lesokhim.prom. 15 no.2:5-7 962. (MUU 18:3)
1. Mookovskcye otdeleniye Gosudarstvennogo nauchno-issledovatell-
skogo instituta gidroliznoy i sullfitno-spirtovoy promyshlennosti.
KMCHKOVA, A.P.; VOROBIYEVA, G.I. ,
Organia acids as a source of carbon for fodder yeasts. Gidroliz.
i.loookhimeprom, 17 no,8:9-3.1 164. (MIRA l8a)
1. VNIlsintazbelok.
VOROBOYEVA, 0.1.; BOBYRI, L.M.
Organic acids of hydrolysis substrates and method for their
determining., Sborotrud,NIIGS 12:129-137 164*
(MIRA 18:3)
r t.
Card ,ib 14 1, ~ I
Authors I Stepukhovich, A. D. aril Vorobyeva, G. !%
Title I Kinc,tics and M-echani3m of hvdroearbon decomuon[tion. : qrt-
Periodical I Zhu- fiz. khim. 8, 1361-1370, Aug 1954
Abatr%at I The effect, of inhibitors (is,-)butylere am proprlene) :~n the
Ca C ;1' W4. qt A r, 1 -R
F jf~ T ii or c d - r- r vo r r-
Institution The N. "hernishevsviv ")t.ate University, `arf~tav
Submitted Octiber 6, 1952 and Decenber 26, 1953
I
ITANCHIKOTA, E.I.t XCLUMOTA. ,T.- NONOBRITEXATA, To H,-, XMTASHOVA,
MSM.; ULIDATMA, 6h,N*/;' K31'1MXVA# B.G.. Priniall uchastlys:
ABDULINA. M.N.; KLIKMO, K.K.; OYSTAIMINA, V.I.: SOKOLOV, N.Y.;
URAZOYA, M.I -TWA@ GoP., AKHKMWA, NOB4, otv.red.;
NOVOKHATSKIT: I.P., red.; SHEYOffUK, T.I., red.: ATTKUKHMETOTA.
S.; ROROKINA, Z.F., takhn.red.
[The Karaganda Economic Administrative Region; bibliography]
Karagandinskii ekonomichaskii administrativnyi raion: biblio-
grafichaskii ukazatell literatury. Alma-Ata, 1959. 458 p.
(KIRA 13:2)
1. Akademiya nauk Kazakhakoy SSR. Alma-Ata. TSentralinaya
naucbnaya biblioteka.
(Bibliography--Xaraganda Econor4o Region)
(Karaganda Economic Region-Bibliography)
USSR/ Physical Chemistry - Kinetics. Combustion. Uplosives. Topochemistry. B-9
catalysis
Abs Jour : Referat Zhur - Khimiya, lqo 4., 195T, "P16
Author : M-A.D. Stepukhovich and 0.1. Kate
IV. A.D. Stepukhovich and G.r. Voroblyeva
V. A.D. Stepokhovich and L.V. Derevenskikh
VI. Stepukhovich A.D.., Stallmakhova L.S., Yeremin VS.
VII. Stepukhovich A.D.,'Derevenekikh L.V*
Title Kinetics and Mechanism of Decomposition of Hydrocarbons.
III. Kinetics and Mechanism of Thermal,Decomposition of Divinyl at Low
Temperatures.
IV. Kinetics and Xechanism'of Decomposition of Iaobutane in the Pre-
eence of Isobutylene and Propylene'as Inhibitors
V. Kinetics of Thermal Decomposition of Gaseous Paraffins in the Pre-
sence of Added Divinyl
VX. Kinetics of Thermal Decomposition of Gaseous Paraffins in the Pre-
seh6e -of Acetyl-ini
VII. Kinitics and Mechanism of Decomposition of Gaseous Alkanes in the
Presence of Allene
Orig Pub Zhurnal fiz. khimii, 1954, 28, No 7, 1174-3.185; No 8, 1361-1370; No 10,
172o-1724; No 11, 1878-1881; 1955, 29, No 12, 2129-2132
1/4
USSR/ Physical Chendstry - Kinetics. Combustion. Explosives. Topochemistry. B-9
Catalysis
Abe Jour : Referat Zhur.- Xhimiya) No 4., 1937) u216
Abstract : M. The velocity constant of divinyl decomposition, calculated in accor-
dance vith the equation of the reactions of second order, varies linearly,
at 570-620o and 2-30 Rg pressure,-depending on 1/po (po-- initial pres-
sure).' Calculatsd vere mean duration of life'of divinyl molecule in activ&-
ted state, 5.10- seconds, the number of kinetically active degrees of free-
dom 20, and dissociaton energy of divinyl 9 = 79.4 1-1.9 kcal/mole. Decom-
position of divinyl conforms to the Dintiess-Frost equation and is interpre-
ted as a chain reaction undergoing spontaneous Eihibition by decomposition
products. 'Additions of divinyl accelerate decomposition of c2u6 at 62oP.
Accelerative action of divihyl reaches a limit at 12%.
IV. By-the methc~ of inhibiting additives (R&Khii, 19530 L 8215) ik study
iids madib'oif thermal decompositi8i of'iaobi!tejie at, priaiiiib'6f'10 nid Ng
and'temperatured"of-548 and 573 - -Addition of 0.5p eldvs'dovn-.the..de'-
composition sharply, on increase OfL the addition from'l to 7% effective-
ness of its action decreasda.,''and'vith 7-10% saturation is reached (fikst
order velocity constant acquires constant'valud),.- Underth6 same condi-
tions inhibition by isobutylene is more effective than by propylene.
2/4
USSR/ Physical Chemistry Kinetics. Combustion. Explosives. Topochemistry. B-9
Catalysis
Abs Jour Referat Zhur FbImiya, No 4, 1957, lm6
ftperimental data on inhibiting action of additives fit the equation:
11W - Woo A + BC (1), wherein W -- reaction velocity, Wo-- residual
velocity, A and B 2- constants, C(add) concentration of additive,
which'proves the chain nature of the decomposition'. The primary'effect
is decomposition of iaobutahemolecule at C-C bond. Inhibiting action
of olefins is explained by removal of H atom by'active radical from fno-
lecule of additive with formdtion'of inactive unsaturated radicals. By
means of equation (1) were calculated velocity constants of the reaction
of chain termination at the wall and at molecules of additive. Activa-
tion energy of inhibiting reactions,brought about by isobutylene and pro-
pylene is, respectively, 5.6'and 8-5 kcal/mole, that of the reaction of
termination at wall, 14-7 kcal/mOle.
V. Study,of'kinetice of thermal decomposition of propane, butane and
iaobutane, in the presenc6 of diviAyl, with initial pressure of decom-
posing hydrocarbons- 10 mai Hg, and at temperatures'of 510-5930. Ad-
ditions of divinyl, which is a product of cracking of hydrocarbons, do
not inhibit decomposition of these hydrocarbons. Absence of inhibiting
3/4
USSR/ Physical Chemistry Kinetiose Combustion* Explosivass Topoohemistrye B-9
Catalysis
Abs Jour t Referat Zhur Khimlya, No 4,-1967, 11216
action of divinyl is correlated'with greater durability of C-H bond, in
CH2 groups, at the double bond carbon, In comparison with durabilit-y of
C-H bond in methyl groups of propylene of isobutylene.
Vre Study of kinetics of thermal decomposition of propane and butanes
in the presence of 1- 20% C2H &i pressure of decomposing hydrooarbons--IL,
mm and temperatures of 50OZ680o, Additions of C H do not inhibit rate
J,2 velocity constant
of decomposition. Xnareased values of decomposs on
of propane at pressures below 10 mm, in the presence Of C2H2, sre due to
the fact that that C2H 2impedes diffusion of active centers to the walls*
Thermal calculations have shown the possibility of a reaction between
stomlo hydrogen and C2H2, with formation of highly reactive vinyl radical
which Is stable under cracking conditionse
V11# Additions of allene inhibit cracking of CJH? and too-C010, but do
not affect decomposition of C4H Methanilsm 0 nhibition resides In ad-
ddition "of H atoms to allens moloacule with formation of little active allyl
radicals,. Absence of Inhibition in the case or C Ao Is due to the fact
that increase of latter occurs essentially with f6mation of CH3 radical*
4/4 Communication rr, see RZhKh1m, 1957, 393.
VO.WBIYEVA,, G.P,
Remats of the Clinical test of aceelidine. Oft.zhur. 16
no.6:352-359 16L. (MIRA 3-4:10)
1, Iz klinfld glaznykh bolezney (zav. - prof* SsFs W Ora) j
2-y Odeeskoy gorodqkoy klinicheskoy bolliaitsy.
(RIOTICS)
,VCRCBIYEVA, G.V.; KIREYEV, Yu.A.; BRATUS, I.N,; VORONIN, V.G,
Production of phenylethyl alcohol from styrene. Trudy VNIISIMV
no,6t48-50 16t - OffRA 1?.-4)
GLUSHCHMIKO, N.N., kand. sellkhoz. nauk; ALEKSEYEVA, Yo.I., kand.
sellkhoz. nauk; VOROBIYEVA, G.V.; LUZINA, L.V., kand.
-1-1-1--z- 1--C m
biol. nauk; IMCIMIKO, G., III OV, B.M., kand. sell-
khoz. nauk; KiSJ-J%TOVA, S.A., red.
[Recomendations for the production of w.omatic plant seeds)
Rekomendatsii po semonovodstvu efiromaslichrVkh kulltur. Mlo-
skva, Sollkhozizdat, 1963. 27 p. (1,11ILk 17:6)
1. Russia (1923- U.S.S.R.) Ministerstvo sellskago khozyay-
stva. Upravleniye nauki, propagandy i vnedreniya peredovogo
opyta. 2. Pauchnyye sotrudniki Vsosoyuznogo nauchno-
isoledovatellskogo instituta maslichnykh I ofiromaslichnyl-h
kulltur. (~O-r all except Krylatova).
-. . I - - ~ i71, I - 4~, - T~
anz ",- ~OIRIOBITXTA _i- -- - -- - -
11~1~~Iiil I - -
Prospects for the use of fluorine plastics in the hydrolysis
industry. Gidroliz. I 1080khlm. Prom. 11 no.9-10- 158.
(Plastics) (Hydrolysis) (MIRA 11:2)
VCROBIUVA, G.7h.; VYRODOVA, Ye.P.
Testing plastic materials in hydrochloric acid media of glucose
manufacture. Gidroliz. i lesokhim.pron. 12 no*ltl8-20 159.
(MM 12:2)
I# Vooequsnyy nauchno-Iseledovatel'okly 1natitut g1drolignoy
i sullfitnoapirtovoy promyshlennosti.
(Plastics--Testing) (Hydrochloric acid)
VOROBITVAq G.Ta.-, VrRODOVAq Ts.P.
I
Chavical stability of graphitic materials in hydroclor'Ver.-mpid
media In the production of glucose. Gidrolix.i loookhim. ron.
12 no.6:8-10 159. (141RA 13:25
1, Vs#jsoyuzW nauabno-Iseledovatellekty Inatitut gidroliznoy I
oullfitno-spirtovoy promynblennostit
(Graphite)
NOVINSKIY. G., vrach; VOROBIYNV, L., inzh,; VcaoBly]WA, I.# biofisik
Diagnosis by instruments. Izobrol rate, no.8.-12-14
Ag 16o. (Diagnosis) (UM 13:7)
(Medical instruments and apparatus)
88917
S/025/60/000/012/005/Cfjlr,
A166/AO26
AL'THORS: Novlnskiy, G.D.; Voroblyeva, I.A.; Physicians; Voroblyev, L.N.,
Engineer
TITLE; Acupuncture Apparatus
PERIODICAL: Nauka i zhizn', 1960, No. 12, pp. 46 - 47
TEXT: The Kafedra biofiziki biologo-pochvennogo fakull-teta Moskovskogo uni-
versiteta imeni M.V. Lomonosova'(Department of Biophysics of the Biology and Soil
Faculty of the Moscow University imeni M.V. Lomonosov) has designed two devices
for finding the exact location of acupuncture points. Research has shown that,
these points, as specified in Chinese medicine, are covered by more friable.con-
nective tissue than normally. This can be detected by an electronic device. When
the electrode finds such a place it causes a neon lamp to-light. In cases where
it is impossible to make use of the electronic device a portable acoustic appara-
tus can be used. This consists of two 6mall metal tubes tipped with rubber caps,
which the physician inserts in his ears. The tubes are then soratched along
certain lines of the body and the physician analyses the reeulting sound. The
acupuncture point is indicated by a weakening of the sound, otherwise the sound
in both ears is the same. The principle of the device is that the s-31.md caused
Ca:rd 1/2
88917
Acupuncture Apparatus
3/025/60/0W/0 1210051004
A166/AC-26
by friction against the body is transmitted dissimilarly through media of dif fenrl",
&-nslty. The dIfference In this case is between normal connective tIss,.ie and the
more friable skin oVer the acupuncture points. Work on improving theze two de-'
vices continues and the scientists concerned are Inves-Agatine the POzsibilit7 :~f
designing a portable semiconductor device.
Card 2/2
ky
VOROBOYEVA, ~1. A,t CAND BIG S019 ON CERTAIN ONARACTER18-
TICS Of THE SIOLOOICAL EFFECT OF ULTRAVIOLET RAYS Of VARIOUS
- ft
WAVELENGTH$& Moscowl 1960* (MOSCOW ORDER OF LENIN AND OR-
A
DER of LABOR RED BANNER STATE-UNI.V Im M. V# Lomomosov), (KLI
2-619 204).
-75-
VIDVIRSKIT, G,D*, vrach; VOROBIMA, I.A9, vrach; VOROBIMO L,R., insh.
Instruments for acupuncture, lauka i shisn' 27 no-12:46-47 D o6o.
(JaU 13:32)
(ACUFMCVM)
VOFDB 'TWA, I.A.
Perforated gastric ulcer in an 11-yearpold boy. Xhlrargila
no.7:83 Jl 155. (W24 8.-12)
1. Is khirurgicheskogo otaeleniya (say. S.I.Repln) BollnUffir
no.12: Sormovskogo rayzdravotdola g. Gor1kogo (glavr4ry vrach
YO.R.Rysev) .
(STOMACH-ULOIMS)
VOROBITEVA. I A,; VOROBOYEV, L.N.
iffoct of adenosine triphosphate on the resting potentlal and
the movement of the Hitella mucronata protoplasm, Biofizi.ka
10 no.6tlOO7-1013 065.
(Hua 19ti)
1. Inatitut biologicheskoy fiziki AN SSSRO Moskvap i Biologo-
pochvenny,y fakulitat MoBkovskogo gosudarstvennogo unIveraitata
imeni. H.V.Lomonosova. Submittod May 210 1965.
ZMTOMIRSKIY, S.I., inshener; V_OROBITAVA, I.A., inshener.
Statistical control of induction motors In factory tests, Test*
elektroprom, 27 no.12:12-15 D 156& (KLRA 10:1)
1. Zavod Imeni Tladimira Illichao
(Rectrio motors--Qualitr. control)
. .1
~WD~VAJ* 1. A. U. a. S.,R.
"Certain peculiarities of Biological action of UV-rays vith different wave
lengths. "
paper submitted for the Third Intl- Congresu on Photobiology, Copenhagen) 31 July -
5 August 196o.
VOROB I MAP- I
11--~.---l'
Iffect of ultraviolet rays of different ways length on the electric
conductivity of the rabbit skin, B&ucb.dokl.vys,obkoly,- biol.tauki
no.2.-173-17? 160. (MM 13:4)
L Rekomendovam Wedroy b1ofisiki Moskovskogo gosudaretwennogo
universitsta im. N.V. Lomonosova.
(ULTBAVIOLET RAYS-PHYSIOWGICAL AMC?)
(SKIN) (ZLZCTROPHYSIOLOOY)
VOROBIYEVAJ, I.A.; POGLAZOVP B.F.
Isolation of contractile proteins from the alga Hitella, flexillo.
Biofizlka 8 no.41427-429 163. (MIRA 17:10)
1. Institut biologicheskoy fiziki, AN SSSR, Moskva i Institut radia-
tsionnoy i fiziko-khimicheskoy biologii AN SSSR, Moskva.
VoRaBlym tychlyan)
Relation between the local and total-body reaction In ultraviolet
Irradiation with different wave lengths, Zhur.ob.biol. 21 no.l:
71-73 Ja-7 t6o. (MIRA 130)
.1. Chair of Biological Physics, Noacow State University.
.(UMRAVIOLIT RATS---PHYSIOLOGICAL ZMCT) (LXUGOCTTtS)
VOROBIYEVA, LI.
Physical culture therapy in the clinical aspects of pulmonary
tuberculosis. Probl. tub. 4;~ no.107-63 164. (MIRA 17:8)
1. Otdeleniye funktBionallnoy diagnostiki i.fiziloheskikh
metodov leoheniya (rukovQditell - kande mod, nauk S.R. La
lachinyan) Mookovskogo nauchno-isoledovateliskogo instituta
tuberkuleza (die,'- kand. mod. nauk T.P. Mochalova, zamesti-
tell;direktora po nauchnoy chasti - prof, D.D. Aoeyev) Minis-
terstva zdravookhianeniya HSFSR.
STEPANOV, B.I.; VOROBIXEVA, I.I.1 ANDREYEVA, M.A.
Subs titution of halogen in azo compounds, Part 14t
Substitution of chlorine in the azo dye of
3-chloro-3-aminoanthraquinone and 2-naphthols Zhuroob,khim,
32 no.10:3281-3283 0 162. (MIRA 15:11)
1. Moakovskiy khimiko-tekhnologicheakiy institut imeni.
D.I. Mendeleyeva.
(Azo dyes) (Chlorine)
(Subatitution (Chemistry))
5M SOV/76-33-7-25/40
AUTHORSt Malitsev, A. N., Yeremin, Ye. N., Voroblyeva, 1. It.
TITLEs On Steady Concentrations of Nitrogen Oxide in Discharge. II~
Experiments With Air and a Narrow Tube
PERIODICALt Zhurnal fizicheskoy khimii, 1959, Vol 33, Nr 7,
pp 1618 - 1624 (USSR)
ABSTRACTt In aprevious pa er (Ref the dependence of the steady con-
centration of Mroger. oxi'le' M r"N .0 on the amperage in pro-
L/V 0
du-,tion from air during smoldering acharge was investigated
in a wide vessel at difforent pressure. In the present cane, 'the
authors checked the same dependence on C6 N03,, in a reacticn
tube at an atmospheric pressure of between 50 and 300 torr.
(I) was synthesized within a range of electric dischargc by
means of a circulation apparatus described already earlier (Ref 1).
A quartz tube was used as a reaction tube (Fig 1) which was
3 mm thick within the range of (.ischarge (diameter of the ranges
32 mm). Measurement results indicate that there are two kinds
of dependences of % Noj,,~, on amperage presents 1) At 50 and
100 torr the steady M-concentration first increases, and then
Card 1/2 apparently approaches a final value; 2) At 200 and 300 torr
On Steady Concentrations of Nitrogen Oxidi in SOV/76-33-7-25/40
Discharge. 11. Experiments With Air and a Narrow Tube
D NO)", pauses,after a sharp rise, through a maximum. In t-e
present tubeq~the concentrations of (1) are higher than in that
mentioned in reference 11 at 100 torr t-hey attained 1..2
.1%, the
highest value ever attained in direct synth031B from air. Thus,
the non-the.-mal nature of activation of the reaction is con-
firmed. Measurements of the dependence of [,d, N01, on the pro-
duot of amperage and pressure (ip) showed a nature similar to
that described in reference 1. The voltage of disobarge was
measured by means of S-95 and S-96 voltmeter3, compared with
measurements on Nom-6 and 'NOLI-10 measuring transformers; the re-
sults agreed well with one another. It was found that th~? re-
lative longitudinal potential gradients are four times lower
than in the reactor (Ref 1). The experimental results obtained
are explained from the standpoint of a chain decomposition of
(I). There are 5 figures and 6 references, 5 of which are Soviet.
ASSOCIATIONt Moskovskiy gosudarstvennyy universitet im. M. V. Lomonosova
(Moscow State University imeni M. V. Lomonosov)
SUBMITTEDs January 10, 1958
Card 2/2
KURSANOV, A L.; KULAYEVA., 0.11.1 SVESIINIKOVA, I.N.; POPOVAP E.A.;
BOZ~;KIIIA, Yu.P.; KLYACHKO, N.L.; VCROBIYFVA,'!.P.
Restoration of cellular structures and notaboll.'sm in yellow
leaves under the effect of 6-benzylaminopurins. Fitiol. rast.
11 no.5t838-847 S-0 16"'Ib (KRA 17310)
1. Timiriazov lns~ttute of Plant Physiology, U.S.S.R., Academy
of. Sciences, Noscow.
KUJAYEVAP O.N.; CHERNY-SHEV, Ye.A.; KAYUTENKOP L.A.; DOLGAYA, M.Ye.;
VOROBIYEVA.-I.P.; POFOVAJI E.A.; KLYACHKO, Y.L.
Synthesis and test of the physiological activity of some compounds
of the kinin series. Fiziol. rast. 12 no-5:902-908 S-0 165.
(WRA 19: 1)
1. Institut fiziologii rasteniy imeni Timiryazeva AN SSSR, Moskva
i Institut organichookoy khimii imeni Zelinskogo AN SSSR, Moskva.
KULAYEVA, O.N.; JRE~~YEVA
Mado, of action of kinetin on protein synthesis. Fiziol. rast. 9
no.1:106-108 162. (MIRA 15:3)
1. K.A.Tisdriazev Institute-of Plant Physiology, U.S.S.R. Academy
of Sc-'~ences, Moscow.
(Protein metabolism) (Kinetin)
RN,
Czwntry : USSR T
v= : Human and Animal Fbysiology, Thermoregulation
Cc. t o
7 or
.
_
1111bo . Tour, : Ref Zhur - Biol., No. 20 1959, No. 7863
.Aut'L-~Dr : V orob I yeva. I,V,
_
'0
`
vanov~
o~~~ Institute
Institlitil :I
Titlo :A Study of the Effectiveness of Steeling Child-
ran to the Cold by Means of Cutaneous Vascular
Reactions*
: Sb. naucbn, tr. Ivanovsk. med. in-ta, 1957,
No. 12, 67--72
,Abotract no abstract
Cara:
61- _A_
-0-MMMOZE ;51_~AMIMMM
NNE FM" M
NITMI W&MMOMOR
GEGUZIN, la.Ye.; OVCIIARMII~O, U.N.; VOROBIYEVA., I.V.
Surface phenomena on single crystals. Mechanism and kiristf-Cs
the filling of deep cracks on the siirface of ionic single
KrIstallografiIa 10 no.3:371-379 My-Je 165.
- 18:7)
1. Kharlkavskiy gosudarstvenny-I univervitet.
SIMIN, Ivan Nazarovichl ANUMW. Viktor Iyanovich; IVANOT, Fedor
MikhAyloyloh. Prinimall uchostlys: VASTUTA, L.G.: TALTUB, T.K.;
VClRO3,'.TZVA, X.G.-I ZHARMA, Ta.P.-, MWJWYA. Ta.Y.; ITANTSMA.
N.I.: ZUBKOVA, M.S., red.; DONSEATA, G.D., teirrha.red.
[Injection intoichannale with stressed reinforcements] Inlakti-
rovanie kanalov a nopriashannoi aruturoi. Moskva, Hauchno-te 'khn.
izd-vo X-va aytomobillnogo transp. i shossainykh dorog. 1960.
23 p. (MIRA 13:4)
1. Gosudarotvenw Vsasoyusnyy dorozbnyy nauchno-lesledovatellskiy
institut (SOTUZDORNII),(for Vasyuta, Talyus, Voroblyeva. Zharova,
Nefedova, lvantayeva).
(Bridges, Concrete)
TOROB I TIM, 1. 1.
Geothermal characteristics of the Oxek-Guat oil field
and otner regions of the Tersk-Kum Plalue Geol,naftl
i gaza 4 no.6s42-45 Je 160. (KM 1337)
1. Grosneneki3r nef tyanoy institut.
(Tersk--Kum Plain-Rocks-Thermal properties)
I
USSR / Diseases of Pam Animis 1 Genbral problems& R
Abs Jour Ref Zhur -i Biblogiya) lid !2., 19~91 N04, 7429
Author kVoroblyeva Ko I*
Z~Ist : CMs'k ~Ae~~~itute
Title :The Effect of a Paraffin Dressing upon Softening
the Horn of a Hoof
Orig Pub :Sbo stud. muohno-isslede raboti Omakly vet. In-t.
1957., VYP 1., 3-4
Abstract No abstract given,
Card 1/1
, VOROBIYEVAL, K.L.; PECHORMA, I-N-Y nauchn. red.
~!-Ie~ ,r
., t!V*w'?~i".1KAk~V
(Industrial eltictronics] Promyshlennala elektronika;
uchabnoe posobie. Sverdlovsk., Ural'skii politekhn. in-t
im. S.I,',.Kiroval 1963. 199 p. WIRA 170)
SEWENKO, M.M., kand.ekon.nauk-; KUGUSHEVq M.F. [Xubusbev2 M.F.];
PRAVDINq M.V,; FOILTCM9 V.I.,-, ALEKSANDR(TVAp V.P.; GORODETSmg
N.1, [Horodetslkyip R.I.]; DYATLOV, T.1,; KALIT-A, M.S. 11L-aytap
Y
M.S.]- DARAGANg M.V. Parahant M.V.b RADIHAv Yu.M.; YMOBrMAL__
j
i-~robyovag, K.T.J; LkSTIVXA, N.N.3 STARODUBSKIY, k-.D.
jSK-arodubstkyip R.D.]3 YATSENK09 P.F.; MUR%TTSEVAg G.M.
[Muromtsevaq HJQ; RASNER, S.I.; CMUIYAK9 K.I.; KOBILYAKOV,
I.I. [Yoby11akL,7, 1.1.]; ALEKSANDROVA, V.0., kand.ekonom.nauk,
otv.red.; DEMIDYUK9 V.F. [Demydiuk2 V.F.jv red.; LrBEUW, TeRep
tekhn.red.
['Ways of increashig profits In met-Murgicil industries] Shliakby
pidvyshchennia rentabelinosti matalurgiixftb pidpryiemstv. Xylvp
Vyd-vo Akad.nauk URSR9 1961. 93 p0
(MIRA 34:6)
I* Akademiya nauk USSRv Kiyev. Ingtitut ekoncmiki. 2. Inatitut
ekonomiki AN USSR (for Seredenkop V.P.Alekaandrovat Nalitar
Daraganp Radima)o 3* DnepropetrovoUy Irbimi o-tekhnologicheskiy
institut (for Gorodetskiyp Dyatlov). 4. Dneprodzorzhinskiy
metallurgichesk1y institut (for Kobilyakov).
(Dnepropetrovsk Province-Steel iindustry-Coato)
VOROBIMA, PfVI'i.fK' f'.Ya.
~;Ix~ylng high--lim-Iw- aft,~:- ill a retorttype
cok'~rig oven, Qgaaurou 30 rjos7:27-30- rJ5, (MTFA 18:E)
1. Voi-,ochnyy imtitut ogneuporriv.
-Va=tWA,, ra,; PEPZPZLn=, VA,
Sorvics of dinas roftuabalm in r m;ppl-, roflnlv# 9brawme
TSvot. not. 38 no.ni6o.65 if #65. (Ian 32sn)
RAGOZINNIKOV, V.A.1 MROI~YEA -V.
Refractory materials for calcining furrAcez. Ognsuporr 29 no.22s
553 '164- (MIRA 18ol)
Is VostoohM inatitut ogneuporovo
0
.1. ~ I
STRELOV2 K.K.; MAMYKIN, F.S,; Priniumli uchastiye; BASIYM, I.F.;
BICIMIRL, A.A.o.BROJII V.A.; VECHZR, N.A.; V I
DOUCHKOVA~,-Z.S.; D'YACHKOV, PA; DVORKI 1 M.M.;
.IGHATOVA, T.S.; KAYBICHEVA, M.N.; KBLAREVO N.V.;
KOSOLAPOV, Ye.F.; MARIYEVICH, N.I.2- MIKHAYLOV, Yu.F.j
SMIKINAl N.V.; STARTSEV, D.Ao; SYREYSIICHIKOV, Yu.Ye.;
TAPWOVSKIY~ G.I.; nYAGIN, V.G.; FREYDENBERG, A.S.;
KHOROSHAVIN, L.B.; ClfUBUKCV, M.F.; SHVARTSMAN, I.Sh.;
SHCHETNIKOVA, I.-L.
Institutes and enterprises. Ogneupory 27 no.U:499-501
(MIRA 15: 1-1)
1. Vostochnyy institut ogneuporov (for Strelov). 2. Urallskiy
politekhnicheakiy institut im. S.M. Kirova (for Mamykin).
(Rafractorylmaterials-Research)
I~,VOROBIYEVA, L.
Letto instruct the activist group in the demando of life.
Okhr, truds, i sots. strakh. 4 no-5:P-3-1 147 161. (MIRA 14:5)
1. Sekretarl Rostovgkogo oblastnogo soveta profsoyuzov.
(Rostov Province-Insurance, Sooial--Employeas)
(Rostov Province-Industrial hygiene)
ZYR rN RLOV, DmItriy Sergeyevlch; VOROWYEVA
MkoIay Georgiyovinhj,01
KORORTSOVA, B.A., red.
[Refereja---* and -alculation tables for the piqsico--,,her,,A:AI
study of soils] Spravochnye i raschetnye tablitsy dlia
fiziko-Ahimicheskikh metodriv Issledovaniia pocir-4. Moskva,
lzd--7e-I Mosk. univ., 1965, A31.p. (IM A 18:8)
,OBIY";,jrp. I - f
YK,; B0110"U'l,"It, 11 V-T I
lnvestignLlq~ (.4,1 mollvirj.!sm ~--f I-,hp fr,