SCIENTIFIC ABSTRACT YAROVENKO. G.I. - YAROVENKO. V.L.

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• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

USSR/C-altivated Plai-ts - Coi-miercial, Su_far-Beari7iL. m
Abs Jour Rof Zhur Blol., No A, 1953, 82433
Author Protasov, P.V., Yarovenko, G.I.
List ---
Title Somm rata on t%e 1afl-,:.e.--ce of A-titiseptics o- Cotto-,i
Yield.
Ori- Pub Sots. s. k1i. Uzbekista~~a
1956, 11o 6, '(1-73
Abstract In 1955, laboratory experiiiei-.ts were carried out at the
Ceatral Statiou of Fertilizers aud Agricitltvxal Soil
Science of the All.-Union Cotton Scientific Researc',l Ins-
tit te for the purpose of a conparative study of the ii.-.
flc~e!,.ce of Nts (as a--; anatiseptic) on t'4-,e dynamics of the
formtio,. of nitrate and aTm.-ioni m N in sierozems. Expe -
rimen,ts were conducted il-, Petri dishes. 100 ~Tams of the
soil ai-d 20 milli~rrams of N i*, the for.-.i of Naa, Ila and
Nts were placed i_-. each disj'.-,, As--~antiseptics, 121~,. hexach-
lormle d,2st (20 milligraris to a dis,,.) avid Nts
Card 1/2
- 87

A
USSR/Caltivated Pla;As - Comcreial. Oil-Ecarii*4.6. Su(pr-Bearii.,C,. m
Abs Jour Ref Zhur Biol., No 18, 1958, 82433
(5 milli,,Ta',13 to n ware applied. The
data s.iow Clat ai. additio.- t,~) VX fertilizers of a
small qumtity of Ilts or :-,emchlorarte is accompanied
with an accm-i.LIatio:_ of nrraonilm N and a slower acidifi-
cation of it to nitrates. Me field test condvcted in
the same year at Sverdliv Kolldioz shwed that an addition
to '~,In of antiseptics (temchlora:.e, yanosan L-ethyluer-
curochloride -:creased t'.:e cotto-.- wool yield
-7, paraforia) j.
oa an avera~-.,e by 3 cc!,ut-.-_ers/ha. The nost positive ef-
fect Da the c,)tto:-. wooi. yield was prod,ced by the 12% he-
xachlovaae d-ist. V.F. Neporailuyev
Card 2/2

USSR Cultivated Plants. Coinmercia--l--.--O-I--I-Beei7ring. T4-- 5
Sugar-Bearing.
Abs Jour: Ref Zhur-Biol., No 6, 1956, 25124
Author Yargveako- G.I-
Inst The ikll-Union Cotton S.R.I.
Title A Contribution to the Problem of the Significance
of Nitrate and Ammonia Nitrogen in Cotton Nourish-
ment
Orig Pub: Dokl. AN UzbSSR, 1956, No 9, 43-46 (Res. Uzb.)
Abstract: By the isolated feeding method in water and soils
cultures the periodic feeding of cotton with nitrate
and ammonia nitrogen was studied at the Central
Station of Fertilizers and Agricultural Soil Science
of the All-Union Cotton Scientific Research Insti-
tute. The variant appeared best in the number of
bolls having formed and the raw cotton yield, where
Card 1/2
107

USSR / Cultivated Plants. Commercial. Oil-Bearing. M-5
Sugar-Bearing.
Abs Jour: Ref Zhur-Biol., No 6, 1958, 25124
Abstract: nitrogen was applied in ammonia form up to the
,beginning of flowering, and afterwards in nitrate
form. Cotton had a higher percentage of peat
damage throughout the entire period of vegeta-
tion in the presence of nitrate feeding. With
ammonia feeding the cotton was somewhat smaller in
growth, had dark green leaves and a very low per-
centage of damage. Cotton's absorption of nitrates
and ammonia from nutrient mixtures of Ca (N03)2 and
(NH4)2SO4 took place approximately in equal quan-
tities. -- A.M. Shchepetillnikova
Card 2/2
t- r

U
m
OL,

r -Y
IuTiAR 11~
T M
M-ad
-aimn, 1
: POPO-la
50
;
-
.
.
.
'
AS Uzbek- SSR
T 11 L Prodeaction Experimanti3 in Nplilying Liquid
Nii--rogen Fertilizers under Cotton ir. 1956.
-
pb,;:~ V eb..- Ref. n8uchr,(.-ILssIed. rzabot po kh1cp-,
.. kovodsDwi. 'Xnnhkeat, All UZSS',R, 1957, 156-179

i~, S T.1-1T Comparative 3ttsdy of liqiuid alm:ionia iind
autmoniato (2,) in the kollrhozes of Uz,'Dek- Ssil
in, on different soils 5howc-d thmm to
bf- equally fffec-tive. In a number of labora-
tai7y tLsts The --ruintility i3C A emder varying
Aoi 1. mriisture and plonting depthn, lt.~ per-
cola-tic)" tile wator flow cil"d Olo of
-ififation ill the soil
raUr
l
,
larovenko G.I

Country : USSR
Category: Soil Science. Physical and Chemical Properties of Soil.
Abs Jour: RZhBiol., Ero 1.8, 1958, No 82095
Author
Inst i AS Uzbek SOR
Title t Influence of Irriptjon Ithtter oh Lhe MovemonL of A=onlum
Nitrogen in 8icrozen Soil.
Orig Pub: Dok. AN UzSSR, 1957, No 5, 45-48
Abstract: In experiments of the Central Station of Fertili-
zation and Agricultural-Soil Science of the All-Union
Cotton Scion"Gific Research Institute in an irrigation
area of I.-ho republics of Central Asia nitrates were
washed to depths of 50 cia in medium loamy sierozem.
The distribut-ion of the liquid ammonia depended on
Card 1/2
Country USSR
Category: Soil Science. Physical arA Chemical Properties of Soil.
Abs Jour: RZhBiol., 1,10 1B, 1958, No 82095
pre-existing moisture ofthe soil. I-Then the moisture
of the soil was 16-18~o' of the weight of the air-dried
soil, ammonia diffused in a radius of 5 - 9 cm, with
the moisture 221,0' - 3 r-m. Without irr'? 'gation anmonia
was concentrated at the site of the introduced ferti-
lizer (horizon 0 - 3 cm). The fertilizers applied
were: ammonium nitrate, ammonium sulfate, a=Onium
bicarbonate, ammonia brand A, and liquid ammonia. --
S. A. Nihitin
I-

USSR Cultivated Plants. Plants for Technical Use. M
Oil Plants. Sugar Plants.
Abs Jour Ref Zhur - Biologlya, No 6, 1959, No. 24965
Author Yarovenko G. I.
_9`6717--fices UzSSR
Inst Aaa(TdEy of
Title Some Data on the Effectiveness of Urea on
Cotton-Plant Sowings
Orig Pub Dokl. AN UzSSR, 1957, No 8, 47-50
Abstract In a field experiment by the Central Station
of Fertilizers and Agricultural Soil Science,
SoyuzN!KhI [All-Union Scientific Research
Institute of Agriculture] (1956), the
effectiveness of NU In the capacity of a
nitrogen fertilizer at the pre-sowing applica-
tion exceeded, and with additional application
under the plant equalled the offoctivoness of
Card 1/2

USSR Cultivated Plants. Plants for Technical Use.
Oil Plants. Sugar Plants.
Abs Jour Ref Zhur - Biologiya, No 6, 1959, No. 24965
Naa* The speed of nitrification of NM in the
sierozem soil oqualled the nitrification
speed of Naa.
Card 2/2
119
MI

COUIM.""?v US 0", R
C. A T -. --Pz rj' 'a 71
ABS). JDIJR. R..ZBIOL 19-579, X0 # 87141
AU T I i OR I ;r o t ov
'It rogen
.c, of Calel,= Cyanamide as a N
I ITLZ
"PCrtilizel" for CwAon.
ptjf3. FYtIcpk,,Dvodstvo, 1557, No 10) 23-26.
A',, --3) 7-1~T On prolonged ,:torav.c- N, loses a part of 14
,,n,
d be c 'ted for deft'cliation'of cotton. (when the
ccntf.nt of 1.1 is less t1tan jlb") . in this co,,,,nx-ertior. the
Central ~'Itat ion of Fertilizers and Agric-ultural L;oil
.:science ~Jnjorj-~ITK):I has cond,12ted in 1c
an iaw-PT cont-ent NC as Certil-izer for
cc -..t on . T'he- c xTE: riment s slr! veed t -11: At, c f 'I ect, ivi-r-rie C~f N. as
fertI.I.izer denand-:, on the time. of j.41-S applic7--ts-on. tarlyl
Preplanting a-,plication of Nr at the timie of autumn- or
pre-~.Iant-ing plcwj-n7, eliminates i-.s toxicity to
and pror-Rotes conversimi of N to r-~-adiiy %ssimiluble form.
Rate of aij:,licartion is 3010-1400 k-,,/hEcttre. This amoumt of
CARD- 112

Country -4
CATE-GORY
A3S.,JOUR. RZBiol., ifo. 195g/, No. 8711~1
AUTHOR
INST.
.TITLZ
ORIG. PUB.
AB-3TRACT N ,-,iakes it possible to increase the yield
by at least 2- ~ccc'~ntners/he c tare. In the Uzbek SSR alone,
30-50 thousand hectares can be fertilized by making use,
of Nc that is not suitable for defoliation.
I.I. Smirnov.
CARD: 2/2

USSR/Cultivated Pla.-Its - Cor:-,~ rci--I. Oil-BearinL;. Sugar -Bcari-,l,,-. 1-1
Abs Jow~ Ref Zhur Biol., No 18, 1953, 82429
Alit'nor Yarove;,Ao, G.Ii
-------------
I:,~st Acade--.!y of Scie;,ces Uzbek SSR
Bicarbzmate of ;u-.m-,ionixm ol-, O-tton PlaritinGs.
Title On Testinr
OriL Pub UzSSR Fanlar Akad. dokaidlari, Dokl. fOl UzSSR, 1957,
No 11, 45-47
Abstract Besults of field a7id laboratory iLivesti_atio--,s carried
otit ill 1956 at the Ce~~tral Statimi of Fertilizers and
AC~Tic-,-Ituxal Science of the All-Union Cottoa Scie:itific
Research Listitate on the stxidy of armonitri bicarbo:Mte
prepared by Moscow Izstitu+.e of Memical MechaAcal
The field tests were co:-.dl.cted in Tashken-
tskayi oblast; o:: typical mcdi-,zi loaniy rAerozen irriLated
lor.C, before a3ai:ist t'--a backLTo,.md of P60 in Vne form of
Card 1/2

USSR/Cultivated I'larts - Coimicrcial. Oil-Bearing. Sugar-Beariiir~. m
Abs Jour Zhur Diol., No 18, 1958, 82429
PC. After application in the foni of top dressinC5,
annonim bicarboimte was cq-,zl in effective --ess to 11a..
Under the co:,_diti=s of Vie hot clinnte of 'Central
Asia, this fertilizer dem-poses rapidly i:-_ storable
(even -tuider the eo',~Clitions of ~;ood storac~e in fitted o-.at
warehoutses the los6es for 4 mo:iths reach 3W. -- A.M.
smirnov

YAROVENKO, G. I., Dand Agri Sci -(diss) "The effect of the form of
nitrogen fertilizers on the yield of cotton," Moscows 1958, 19 ppj
150 cop, (Sci Res Institute for Fertilizers and InBectofungicides im
Prof. Ya. V. Samoylov) (KL, 45-60, 127)

USSR
ncd. Mineral Fertilizers*
r T: 0- 0 Sail Scie

1 T .
th -Effectiveness of
f Litiseptics ia Ineree'aing e
TME, The Role o
-IrrIgated Cot,oa Yields
on
.
Hitrogren Yartilizars

r;'~JC,,, ?Uji, h.., .19rig, I;o. 2. 3144
Udabraniya i uroz
-VOwing collectlYe
rried out Oil 000,011
7 ?jejcj experiments ca
(the soil. .13 typical sterozem with
fmrms of Uzbokistau
-e)showed that the aimultaneous I
litu
I
.
long-atandinp cotton cx
.
and an antiseptic NA )__
of N
in
l
av
g
aa
und6r p
Introduction
-- sharply inhibite thal
lindarta , paraforpl, and granovan
aad denitjIfying bacteria, thus
l
f
b
ng
y
via,70ility of Uitri
through denitrificatlo
eliminating the p6sisibility of H loss
ter procipitition.
i
-w
n
lavd, Waah-out of N nitrate by autumn
/hectare of
0 jr
f
g
3
tio); undAr plowing O
Thus, the introduc
(12% lindane dust,
i
c
iz + 6o kg/hectar6 of antisept
rowth of cotton, the
h
e g
Oaform or granosan) Increased t
p
Cavd.

pas
iT. y

Jount.
lo446o
2-1 1;59
~

71 U
ODIC,. FuD.
nuxbar of bolls on the pla'ats,
and thO Yield of cottar, wool 1
by 3-4 ce"t"ra/hec tare 14 lom
partson with N
n-lone, 111tr.-

ftA
duced In the 3=0 dose under plowing or an a top dressing.
The application of lindane
duet producad the ~reatezt
effoct.
lit , aPPlied under Plowing at the rate Of 30 kg/hecl
-
tare instORI Of 11 .. abowod sjrj&jot.:ouF, &CtiOn.
Similar
results were Atarned In another field erperfine t. Laboratoiy
n
A
iryes t i9at lot's (expariyaen* in Petri dishoo) %~rjif the addltio~
to N., or 11, of emall doses of 1indane and ); dua t was
ts
accompanied by a considerable accumulation of ammoniuz 1;
and by its slower oxidation to nitrates.-O. P. Medyedeya
Card:
212

40 19 1 57_3~c
-i ir
Cotton Grawin
S RcesearcR71tist (Ilzbek SSR
1, 1 If: ~e; --Effectiverlc-&S Of Presowin,~C Piacement of Ammonia
SIA fate under. Cotton.
r !T-1 .Y!.J-
Flndlngn of experiments of the certral atatjoA
of' fel-tilizers and agrici;1turnI so4l sclerice Of
the co*ton grrow1ng refiearnh Inp-AltlAR.
of Uzbek ~;LIJH, and aleo an exPerimen-J, of thp ap
I ,rl- 1:
Cultural Chemistry laboratory of the China Zskea.17,,a
MTS on the advwitvge of Njj Aa compared w1th INRA
In -aBG of presow-Ing placeme-nt of Na under
cot~ort (In' slerozemal at. a rate of 25 tc 30 % of
tho annual quota. Org-an'!zatianal e'conomic advant-
ai~,ea of this -Tethod are aleo Indicated.
()V~_m rw
yRp
x1luH Ta Y
A
WTHOR
.ITLE
IRIG. FUB.,
tiv~ t-d C
~-u 9, 15731
RZhBiol. .195
lliotpso-
A 1-unl6h cot
PreDoWil-16 Placement of Liquid Nitrogen Ferti-
lizers under Cotton.
1-110-39 35-38
.The economic estimates and findings are cited
of experiments Of the central station of fertill-I
Zer-s and agrosoll science of the All-Union Cottonj
scientific Research institute for 1957, conductedl
ber of kolk'hOZY Of the Uzbek,
in slerozems in a num ~Jng part of the
SSP, on the advantages Of Plac
liquid fertilizers amountinS to 30 % of the annual
N quota under Ploughland as compared
to using the entire annual quota of liquid
ammonia onlY as supplementary fertilizer In the

14n., 57 3 1
T.
ORM..
Perloa me presowing Placement
of psrt of the liquid ammonia beightened thp
raw cotton crop yield and roduced the capital
inveBtffients In the construction of warehoure
-pre"I-A gee.
2 12

YAROVWOO G.L,
Xffect'of wateringonthe efficienc7 of nitrogen fertilizers*, Dokl,
AN Uzb. SSR no.):55-5rt 158. (XIBA llt6)
1. ?Sentraltuaya stantoiya udobrenlya i agropochavoyedonlya Whuchno-
issladovatellskogo khlopkovogo'inatituta Uzbeksko7 akademileel'sko-
khozyaystvennykh nauk..Predstavleno chlenom -korrespondentom AN UzSSR
A.M. Xalltsevym.
(Nitrates) (Fertilizers and manures)

TAROTIMp- --G#Iq
Iffect of benzene hezschlorlds on the effeciivensis of a~monlun
niirsts plowed'under before cotton seedlng,* Bokl, AN VwSS2
no.507-49 1580' (NIRA 11:8)
1, Tft~trallmya stantsiya udolbrenly i agropochvovedeniya Soyunogo
nauchno-lealedovateltakogo khlopkovogo institute, Akaderdi sell-
skokhosMetvewjykh nauk UzSSR. Predatavleno daystvitell"a chle.
nom Aksdsmii sellskokhozyaystvannykh nauk UJISSR S.W. I~rzhovy
036nzene hexachlorlds) (Ammonium nitrate) (Cotton)

UROITNKO' G.I.
Zffect of form of nitrogen fertilizers on the nitrate and amonium
nitrogen in Sierozex soils, Dok. AS UzSSR no.lo:41-44 '56-
(MIRA 11:12)
1. TSentralinaya stanteiya udobreniya i agropochvovedeniya
Vsesoyuznjjjo nEkuchno-issiedovatel'skogo institute. khlopkovodstva
Akademil, sellskokhozMstvennykh nauk UzSSR. Predstavleno akade-
mikam Akademit sel'skoldiozyaystvennykh nauk U25SR S.N.Ity2hovym.
(Sierozem soils) (Fertilizers and manures)

YAROVENKO, G. I.
Testing the effect of ammonia water on cotton plantinV . Dokl.
AN Uz.SSR no.12:55-57 '58. IMM 12:1)
1. TSentrallnaya stantsiya udobrenlya i. agropochvovedenlys
Vs9soyuznogo nauchno-iseledovatel'skogo Institute. khlopkovodstva
i Akademlya sel'skokhozyavBtvonnykh nauk UzSSR. Predstavleno
deyetvitel'n.7ya chlenom AlGademil sellskokhozyayBtvannykh nauk
UzSSR N.M.14annanovym.
(Cotton-Fertilizers and manures) (Ammonium hydroxide)

YAROVENW
Time for applying liquid nitrogen fertilizers to cotton. DALAN
Uz.SSR no,3:47-49 159S (KM 12:7)
1. TSentralInaya stantsira udobraniya i agropochvovedeniya Vsesoyuz-
nogo nauchno-issledovat-31'skogo Instituta kblopkovodstva. Pred-
stavlono deystvitel'nym chlenom Akademli seI'skokhozyaystvenrWkh
nauk UzSSR N.M.Kinnanovym.
(Cotton-Fertilizerg and manures)

UMAROV, A.A.; YAROVENIKO, G.I.
-
Effect of ammonia and nitrate mutrition -- '- -Tnent end
yield of cotton under the conditions of va . .11. ~ *-- Uzb
rying watrr;" ,,- 4. 6
biol. zhur. 7 no.l.*17-19 "63 UMIA 17t7)
1. Vsesoyuznyy ordena Lenina nauchno-isoledovatellskiy institut
khlopkovodstva.

YAROVENKO, G.I.; UMAROVI A.A.
Effect of the size of of urea-formaldehyde fertilizero
on the biochemirril capac-l".y of soils for nitrate a.,cumulation
and the yield of cotton. Uzb. bioll. zhur. 7 no.6-.62-66 163.
(MTRA 17:6)
1. Vsesoyuznyy ordena. Lenins. nauchno-isoledovatellskiy inatitut
khlopkovodstva.

YAROVENKO G...; Ellf, 'r.r!.
Effect vf and rhyllo~:Id~tl do.:ies of on
the blological capacity 91" nrlls to Lho nitraro
0
developmorit, and field of thr, !~otl'~on plont, (Jzb. biol. zhur.
8 no.2il5-17 164. (MIRA 1.7,,!)",-
1. VsesoyjznTf nauchno-iq,3iedo-.,ii,.rillsk'Ly
Tashkent.

USSR/Cultivated Plants - Thchnical Oleaccae, Sugar Plants M-7
Abs Jour : 'Ref 2rhur - Biol., No 1, 1958, 11o 1690
Author : I.P. Yarovenko
Inst : not Given-
Title : An Attempt to Grow Sugar Cane in Uzbekistan
Orig Pub : Sots. s.kh. Uzbekistana, 1956, ITo 10, 64-67
Abstract General description of a 10-year attempt to grow sugar
cane in the Khazarbag sovhoze is given. The methods of agro-
techny (periods and methods of planting, system of cultivating
the soil, fertilizers, irrigation, means of fighting pests
and diseases), which permitted the yield to increase from
100 to 160 (in the initial period of application) to 500-
550 c/h during the years 1952-1953.
Card 1/1
MARFMN, A.S. (tt-,anslatorJ; PETROV, V.P., redaktor;-D-R9X,,~1591, M.Te.,
redaktor; DWRI, I-Ya-, tekhnicheskiy redaktor.
[relLispars; second collection of articlOs- Translated from the
English by A-3-Marfunin] polevye shpaty; 2-1 sbornik statei-
Perevod s angliiskogo A.S.Marfunina- Pod red. V.P.Petrova. Pro-
disl.V.P.Patrova I A.S.Marfunina- Moskva, Izd-vo InosU%nA0i
lit-ry. Vol.2. 1956. 366 p* mu 9:6)
(Ireldepar)

YAROVMO, N.N.; MOTORMYT, S.P.; KIRINSKAYA, L.I.; YASIL'YZVAO'
Reaction of halide anhydrides of fluorinated carboxylic and
thlocarboxylic acids with sedium asides. Zhur. ob. khim. 27
no.8:2243-2246 Ag 15?. NLRA 100)
(Sodium azide) (Acids, yatty)

YAROVENKO, II.N.; MOTORM. S.P.: KIRKNSaYA, L.I.
Formation of difluoroketene and its ploymer. Zhur.ob.khim. 27
no.lo:2796-2799 0 157. (mIRA JI.-4)
(Ketone) (Polymerization)

TMY=O, N*Nw-, VASILIMA, I.S.
New means of Introducing trihalogen methyl group into oreanic
compounds. Zhur.ob.khim. 28 no.9:2502-2504 S 158. (KIRA 11:11)
(Netbyl gr(mp)

-----------
YAPDVMO. N.N.; MOTORNYf, S.P.
Preparation of N-trifluomethylthiocarbamic acid asters. Zhur.ob.
khim. 28 no.9:2504--2303 3 138. (KIRA 11:11)
(Oarbomio said)

TAROYMO, N.V.
Properties of organic compounds in the light of the Mendeleev
Periodic Law. Part 1: Boiling temperature of fluorine compounds
and other halides, Zhur.ob.khim, 28 no*9.-25o6-2$oq s 158.
(MIRA,11:11)
(Hologen compounds) (Boiling points)
-WR ~ MR MR

5 ~3 )
AUT ORSt 'Yarovenko, N. N.,-Gaziyeva, G. B., SOV/79-29-3-38/61
11., Fedorova, 11. A.
TITLE: Syntheses of Organoselenium Compounds Using Carbon Selenid.e as the
Initial Product fSintezy selenoor-aniCiLeskiKn
s6yedineniy, iskhodya iz selenougleroda)
PERIODICAL: Zhurnal obshchey khimii, 1959, Vol 29, Nr 3,
pp 940-942 (USSR)
ABSTRACT: The aim of the investigations reported in the present
paper was the synthesis of new selenium compounds,
u3ing carbon selenide as initial product. Carbon selenide
is known to be one of the simplest and best accessible
selenium carbon covoounds. It is formed in the reaction
of carbon tetrachloride with phosphorus pentaselenide
(Refs 1,2), cadmium selenide (Ref 3) or with hydrogen
selenide, as well as in the heating of elementary selenium
with methylene chloride in the nitrogen current (Ref 5);
the last method is considered the best. Carbon selenide
readily reacts with chlorine under formation of
Card 1/3 trichloromethyl selenium chloride (Ref 5)
I 171T
JZ4

S.yrtilesea of Organoselenium Compoundr Using Carbon SOV/79-29-3-38/61
Sele4i& as;he Initial Product
C12
CSei-na 3SeCl. At low temperatures it is possible to
obtain higher yields (up to 73~) of trichloromethyl
selenium chloride. The authors found that the latter
readily reacts with potassium cyanide under formation
KCN
of trichloromethyl selenium cyanate; CCl 3Seel bM 3SeCH.
In the reaction of trichloromethyl selenium chloride with
ethylene trichloromethyl- chloroethyl selenide is formed:
CH2-CH P-
Ccl3SeCl , Ccl3SeCH2CH2Cl. In the reduction of
trichloromethyl selenium chloride with metallic tin in the
hydrochloric acid medium the dimer of the selenium carbonyl
chloride is obtainedt M 3SeCl Sn -'~(CC12 Be )2' In the
Card 2/3 reaction of carbon aelenide with selenium dioxide the

Syntheses of Organoselenium Compound.- Using Carbon SOT/79-29-3-38/61
Sele~dideas the Initial Product
SeO2 + oleum
carbon selenium oxide is formed: CSe2 CSeO.
There are 5 references.
SUBMITTEDs r-ebruary 7P 1958
Card 3/3

5(3) SOV/79-29-7-12/83
AUTHORS. Motornyy, S. P., Kirenskaya, 1. Iap Yarovenlko, 11. N.
TITLE: New N-Trifluoromethyl Carbamidnates
(Novyye efiry U-trift6rmetilkarbaminovoy kisloty)
PERIODICAL: Zhurnal obshchey IchimUp 1959, Val 29, Nr 7t PP 2157-2159 (USSIO
A13STRACT: According to data from publications fluorinated alkyl
isocyanatos show a high reactivity (Ref 1). They enter
especially easily reaction rith alcohols and phanols to forr.
esters of 11-perfluoro alkyl carbamic acid, o.C.
CH3Oil
'& 17 CH
RFI*ICO - 1011C02 3
Card 1/2
In papers published earlier by the authors(Rof 2) the reactions
of trifluoromothyl isocyanate with halogen hydracid and
mercaptans were deocribed. Since the investigation of the
chemical propertiob of alkyl isocyanatos and their fluorinated
derivatives is of certain -interest, the present paper deals 7ith
the csynthesis of some neTr 1.1-trIfluoromethyl carbcminatas. -The
constants and analytical data of the nev cozpourz1c are tabulated.

New 19-Trifluoromethyl Carbaminaten SOV/70-20-7-12/83
Trifluorometliyl.isocyanate roacts with normal alcohols under
strong heating. For this reason the reaction of the equimolecu-
lar amounts of trifluoromethyl isocyanate and alcohol was
carried out in a closed glace ampoule with intonae cooling.
Yields were 55 to (in individual cases) 70-05 More details
are given in the experimental part. There are 1 table and
2 Soviet references.
SUBMITTED: Juno 6, 1958
Card 2/2

5(3)
AUTHORS: YaroygOo Ne, Rakaha, M.As 50'1/7~-29-7-12//83
TITLE: Fluorination by Mcanc of oC-Pluorinated Aninco
(Ptorirovaniye a pomoshchtyu o,,,ftorirovannykli auinov)
PERIODICAM Zhurnal obahchey khimii, 1959, Vol 29, Nr 7, pp 2159-2163 (USSI)
ABSTRACT: In the investigation of the chemical properties of
cc-fluorinated amines the authors succeeded in cynthesizing
new organofluorine compounds. They found that the amines
RCF2ITRI2react with alcohols to form alkyl fluorides. This
reaction takes place easily with a simple mixing (yield up to
66 Ifa )(S cheme 1). The reactions of the fluorinated amines
RCF2NR2were carried out in a similar Tray with carboxylic acidsg
with their salts or with thiocarboxylic acids under the formation
of acid fluorides of carboxylic acids (Scheme 2). According to
references I and 2, also the reactions of ce-fluorinated aminos
take place Ttith H2S and H2Se under the formation of the hitherto
unknown dialkyl amidos of fluorinated thiocarboxylic and
Card 1/2 selenium carboxylic acids:

Fluorination by Means of C~-Fluorinated Amines
SUBMITTED:
SOY/79-29-7-13/63
OHFC1CF N(C 11 2
2 2 5 27';--~ urcim(v 2115)2
CHF2 CP2N(C 2H5)2 H2Se 30 CHP2CSN(C 2H 5)2
CHF 2CP2N(C2H5)2 CHF,CSeW(C2N5)2
The high mobility of fluorine atoms in C>6-position to nitrogen
and the ease with which they may be replaced by elements of
group 6 may be explained by pe-conjunction (Ref 4). The
fluorinated amines necessary for these reactions are obtained by
the reaction of the secondary amines with fluorinated olefines
(Refs 2, 3) which takes place especially easily in the case of
addition of secondary amines to trifluoro chloroethylene(Schome4).
There are 5 references, 2 of which are Soviet.
June 6. 1958
Card 2/2

50) SOV/79-29-7-14/83
'AUT110113; Yarovenko, N.H., Motornyy, S. P., Vasillyeva, A.B.,
~-Uemr d nod
TITLE: Difluoro Chloromethyl Sulphene Chloride
(Diftorkhlormetilaullfenkhlorid)
PERIODICAL: Zhurnal obshchey khimii9- 1959; Vol 291 Nr 7, pp 2163-2165 (USSR)
ABSTRACT: The purpose of the present paper was the synthesis of the above
compound.In contrast to trichloro methyl sulphene chloride, the
product of its reaction with'diethyl amine, trichloro methyl-
(N-diethyl)-sulphene amide, reacts with antimony trifluoride
in the presence *of small amounts 'of SbCl 51 without separation
of the C-S bond, to form fluorodichloro-,difluorochloro-, and
probably trifluoromethyl-(N-diethyl)-sulphene amides. In this
connection heating and its duration play an important part.
Belov 650 practically only fluoro dichloromethyl-(N-diethyl)
sulphene amide is tormed. At 670 and after heating during 1 1/2
hours difluoro ohloromethyl-(N-diethyl)-sulphene amide (25 %)
in formed in the mixture with fluoro dichloro- and trichloro
methyl-(N-diethyl)-sulphone amide. Since difluoro chloromethyl-
Card 1/2 (N-diethyl)-sulphene amide is very unstable, it is not necessary
T~

Difluoro Chloromethyl Sulphene Chloride SOV/79-29-7-14/83
to separate it from the reaction mas3. The liquid nust only be
separated from the solid, resinous reaction products and then
saturated with dry HC1 (Ref 4)(Scheme 3). The thus obtained
mixture of trichlo-ro-, difluoro chlorc-, and fluorodichloro
methyl sulphene chloride may easily be separated by distillation
in a column. The effect of temperature and the duration of
heating on the yield of difluorochloro- and fluorodichloromethyl
sulphene chlorides may be seen from a table. There are 1 table
and 4 references, i of which is Soviet.
SUBMITTED; June 6, 1958
Card 2/2

MR
TAROVMIKO, N.N.1 RAKSHA- M-AP; SHEMOINA, Y.N.
Synthesis of Wogenated ble (alkyl) diselonides and vy=etrlcal
bla (ohlorodifluorometbvl) disulfide. Zhur. ob. khim, 30 noPI2:4069-
4o?i 3) l6o. (XIU 13:12)
(Diselonide) (Disulfide)

UROVINKO.--It.L; MOTORM, S-P.
Kethode of synthesizing fluorine analogues of dichlorofornoxise.
Zhur. ob khim- 30 no.120o66-4o69 D 16o. (KRA 13;12)
(Formaldebyde)

87535
S/079/60/030/012/020/027
573 600 BOO1/BO64
AUTHORS: Yarovenko, N. N. and Raksha, 14. A.
---------------------- -
TITLE: Synthesis of Tetrafluoro Dimethyl-diselenide and Some of Its
Properties
PERIODICALs Zhurnal obshchey khimii, 1960, Vol. 30, No~ 12, PP. 4064-4066
TEXTj The authors found already in a previous paper (Ref.1) that - anal-
4-
ogoualy to hexafluoro dimethyl-diselenide - the'tetrafluoro dimevhyl-di-
selenide (CF 3Co 2)2Eg 8 3,CF 3SeSeCF3
(CHP 2CO2)2Hg Se ~CHF2SeSeCHF2
is formed in the decarboxylation of the mercury salt of difluara acetic
acid in the presence of selenium. A comparison of these reactions with the
well-known reaction of trifluoro acetic acid salts with sulfur (Ref.2)
shows that the decarboxylation of fluoro carboxylic acid salts in the
presence of the elements of group VI may proceed in two directions. The
reaction depends on the position of the salt former in the periodic table%
Card 1/2

67535
Synthesis of Tetrafluoro Dimethyl-diBelenide S/ON60/030/012/020/027
and Some of Its Properties B001 3064
RC i~~ (RCO)20 + B02 (1)
me Se
0 CRSeSeR (2) (R - alkyl fluoride).
Apparently, also at a further rise of the atomic number of the element,
a decomposition of the salts in direction (2) occurs. It may be assumed
that in the reaction of tellurium with salts of fluorinated carboxylic
acids, fluorinated dialkyl ditellurides are formed. Difluoro methyl
selenium bromide CHF 2SeBr resulted from the reaction of tetrafluoro
dimethyl-diselenide with bromine. It reacts readily with calcium cyanide
under the formation of difluoro methyl selenocyanide and adds to
ethylene under the formation of difluoro methyl-p-bromoethyl selenide-z
KCN ---1 CHF SeCN
CHF 2SeBr CH CH 2
--2 2, CHP2SeCH2CH2Br
There are 3 references: 2 Soviet and 1 British,
SUBMITTED: January 11, 1960
Card 2/2

87536
S/07Y60/030/012/021/027
BOO1 B064
AUTHORSs larovenko Raksha, M. A., and Shemanina, V. N.
TITLE: Synthesis of Halogenated Dialkyl Diselenide and the
Symmetrical Tetrafluoro Dichloro Dimethyl Disulfide
PERIODICAL: Zhurnal obshchey khimii, 1960, Vol. 30, No. 12,
pp-. 4069 - 4071
TEXT: Considering the papers of Refs.1-5 on the synthesis of the
halogenated dialkyl selenides, the authors found that the fluorinated
dialkyl diselenides are also obtained when monoselenium bromide is
reacted with tetrafluoro ethylene:
seep CP Br
1 2 2
Se Br + CF ~ CF This reaction is very sensitive
2 2 2 2 SeCF2 CF 2Br
to temperature and longer heating. The best dise~ enide yield is obtained
by gradually heating the initial products to 160 C in an inert solvent.
When the reaction mixture is rapidly heated to a high temperature, the
monoselenium bromide brominates the diselenide under the separation of
Card 1/2

87536
Synthesis of Halogenated Dialkyl Diselenide S/079/60/030/012/021/027
and the Symmetrical Tetrafluoro Dichloro B001/Bo64
Dimethyl Disulfide
considerable amounts of elementary selenium. The structure of the
diselenide obtained was confirmed by a chlorination to 2-bromo-1,1-2,2-
tetrafluoro ethyl selenium chloride (BrCF2CP2SeCl). Some halogenated
alkyl selenium halides may be reduced to halogenated dialkyl diselenides
(CF3SeSeCF3). 2,21-dichloro diethyl diselenide may be obtained by
reacting 2,21-dihydroxy diethyl diselenide with concentrated hydrochloric
acid. The initial product for this reaction was obtained by reacting
ethylene oxide with H2Se under pressure. The dialkyl diselenides obtained
are colored, bad smelling liquids which are insoluble in water. There are
8 referencest 4 Soviet, 3 US, and I British.
SUBMITTED: January 28, 1960
Card 2/2

27504
S/079/61/031/009/005/012
D215/D306
AUTHORS: Yarovenko, N.N., and Vasilleva, A.S.
TITLE: Dichloroperfluorodivinylsulphide and sulphides
with i7ionofluorochloroethyl group
II.TMIODICAL: Zhurnal obshchey khimii, v. 31# no. 9$ 1961,
3021 - 3023
TEXT: The work was conducted to establish the order of addition
of sulphur monochloride and'hydrogen sulphide to fluorinated ole-
fines under pressure and the action of light. It has been estab-
lished that when a mixture of hydrogen sulphide and trifluorochlo-
roethylene is irradiated in a sealed ampoule, in the presence of
benzoyl peroxide, dichloropei-fluorodivinyleulphide and its poly-
Riers are obtained,
CP2 CFC1 HP
H2S (s'OF2 C11M. )21 S(CF CFC')2 + 1S(CF
Card 1/4 cpcl) 21n

27504
S/07 61/031/009/00.5/012
Dichloroperfluorodivinylaulphide .. D215YD306
Vhen sulphur monochloride and vinyl fluoride are reacted under si-
milar conditions, 2,21-di-fluoro-2,21-dichlorodiethylsulphide is
formed
CH2 OF
32C12 S(C11 2C'fFC')2 + S'
The structure of this compound is confirmed by the inertness of
all C-Cl and C-P bonds. Prolonged stirring of the compound in wa-
ter at room temperature fails to produce ionic fluorine-or chlori-
ne. In compounds with one 2-chloroothyl group and one 21-fluoro-
21-chloro- or 2,21-difluoroethyl group only one chlorine atom of
2-chloroethyl group.,is easily hydrolized. These compounds were
prepared by reacting 1-fluo.-o-l-chloro-2-bromoethane, 1-fluoro-
1,2-dichloroethane and 1,1-difluoro-2-bromoethane with sodium 2-
hydroxyethy1mercaptide followed by substitution of the hydroxyl
group with chlorine
IJOC112CII.SNa CH2BrCJ1FC1 . /CI12CHFCI SOCII, S/C112C11FC1
\CllzcH,OH \C'12C:IIICI
Oard 2/4

27504
S/07 61/031/009/005/012
Dichloroperfluorodiviriylsulphide ... D215YD306
I
Tile order of addition of sulphur monochloride to vinyl fluoride is
confirmed indirectly by the fac 't that when sulphur monochloride is
reacted with vinyl chloride 2,2,21,21-tetrachlorodiethylsulphide
is produced and the latLer hydrolyzes in water to form dia,ldehyde
proving Ito otructuro
S(C11,c1
S2C1 CIL I'CI2)2 E'-O), S(cfhc~ 10),
Preparation of ~,21-difluoro-2f2'-diclilorodiethylsulphide involved
sealing 20-3 9 of*32C12' 18.5 g of vinyl fluoride and 0.2 g of ben-
zoyl peroxide in an ampoule and irradiating the mixture with a
500 17 lamp for 200 hrs. Vacuum distillation yieled 9 g of fraction
b.Pt. 78-79OC/9 mm, nl7 - 1.4813, dl7 _ 1.4550, corresponding to
D 4
the formula C411 6SF2 C12* 2,21-difluoro-2*21-dichlorodiethylaulphine-
p-toluenesulphonylimi.ne m.pt. 1390C corresponding to the formula
Card 3/4

27504
S/079/61/031/009/005/012
Dichloroperfluoi-odivinyloulphide ... D215/D306
Olf306H4 so2NS(CH 20f'FC1)2 was prepared by shaking 0.02 q.mol. 2,21-
difluoro-2,21-dichlorodiet.hyloulphide with CH 3C61I4S02NNaCl. 31120
solution for 1 hr. and recrystallization from alcohol. 2*,2,2121-
tetrachlorodiethylsulphide was prepared by irradiation of a mixtu-
re of 0.2 q. mol. S 2C121 0.2 g benzoyl peroxide and 0.2 g mol. vi-
nylchloride for 15 days. Vacuum distillation yielded 36 % C2H6SC1 4
b.pt. 1060C/8mm, n 23 _ 1.500, d 23 1.5823 2-fluoro-2p2l-dichloro-
0 15 _ 1.50509 d15 _ 1.3301v
diethylsulphide, b.pt, 102 0/16 mmv n D 4
2-fluoro-2,21-dichlorodiethyleulphine-p-toluenesulplionylimine m.pt.
119.50C; 2,2-difluoro-21-chlorodiethylsulphide b.pt. 770C/23 mm,
n14 - 1.4675, d14 1.3501, and tetrafluorodichlorodivinylsulphide
D 4
b.pt. 64 0C/748 mm, n20 _ 1.3984, d20 _ 1.5160 were also prepared.
D 4
SUBMITTED: July 23, 1960
Card 4/4

YAROVWO, NX.i RAKSHA, M.A.; GAZIYEVA,, G.B.
Now methods for the prepsration of efftwe and oelenionvaeld
ester halides. Zhur.ob.khim. 31 no.12s/+006-4010 D 161.
(KUtA 15t2)
(Selenious acid)

YAROVENKOp-N.N.; RAKSHAO M.A.
Reaction of difluoromethyldifluoroacetate with potassium fluoride.
Zhur.ob.khim. 31 no.12:4011-4012 D 161o (MIRA 15:2)
Acetic acid)
tassium fluoride)
W

RAKSHA, M.A.; YAROVENKO, N.N.
Reaction of difluoroacetates with arsenic,, arsenic trichloride,,
and nitrosyl chloride. Zhur. ob. khim. 32 no.1:273-274 Ja 162.
(MIRA 15-2)
(Acetic acid) (Arsenic chloride)
(Nitrosyl chloride)

YAROVENKO, N.N., doktor khimJ.cheskikh nauk
Psychotomimetic agents. Zhur. VIM 9 no.4!448-455 'U.
(MIRA .17:20)

YAROVENKOR 0.; MIROSHNIK, A.
Use of diffusion screens in rotary apparatus. Sakh. prom.
37 no.8t7l Ag 163. (MMA 16:8)
1. Glavnyy inzh. Krasnyomskogo sakharnogo zavoda (for Yarovenko).
2. Glavnyy tekhnolog Krasnyanskogo sakharnogo zavoda (for Hiroshnik).
(Diffusers)

SILIN, P.M.; LITVAK, I.M.; BARABANOV, M.I.; LIKHITSKIY, M.Kh.;
BODNARIJ, S.G.; ROSTRIPENKO,, I.A.; SOFROIUM, L.P.;
YAROVENKO, O.A.; MIROSHMIKp A.P.; IVASEMKO, G.
Accelerating the sedimentation in settlers. Sakh. prom. 36
no.7:9-17 J1 162. MIA 17:1)
1. Moskovskiy tekhnologichesIdy Inatitut pishchevoy promysh-
lennosti (for Silin). 2. Kiyovskiy tekhnologicheakiy institut
pishchevoy promyshlennosti imeni Mikoyana (for Litvak,
Barabanov., Likhitskiy). 3. Linnovskiy Bakharnyy zavod (for
Bondar', Ivasanko). 4. 2-y im. Petrovskogo sakharnyy zavod
(for Rostripenko). 5. Gindeshtskiy sakharnyy zavod (for
Sofronyuk). 5. Krasnyanskiy oakharnyy zavod (for Yarovenkoy
Miroshnik).

YAMVENKO 0 V, I BAYKO V. F.
2. U= (600)
Soils-Analysim
7. Problem of early spring U-Ilage of the voil. Fochvovedents. No. 10, 1952.
List of Russian Accessions, Library of Congress, JanuarY -1953. Unclassified.
"V M.-
a

YAROVINKO, VA.
Sterilization of fermentation vats in continuous fermentation. Spirt.
prom. 20 no-3:14-17 '54. (MI2A 7:10)
(Sterilization) (Yermentatioa)
~S' '1,F

TAROV19KO,V.L.
Investigation of the movement-processes of liquid in a fermentation
vessel and battery. Spirt.pron.21 no.2:6-10 155. (NIJIA 8:10)
Ysesoyusnyy tanchno-iseledovatel'okiy.,institut sakharnoy pro-
myshlonnosti.
(Fermentation)
ffil
.77.

USSR/Chwical Technology Chemical Products and Their Application. Per-mentation
Industry, 1-27
Abst Journal: Referat Zhur - Khimiya, No 19, 1956) 63542
Author: Yarovenko., V. L.
Institution: None
Title: Effect of Conditions on Displacement of Liquid in the Vessels of a
Fomentation Battery
Original al
Pekiodicalf. Spirt. Prom-lat',-1955, No 3, 15-19
Abstract: Effectuation of continuous fomentation of starchy raw materials
necessitated the carrying out of laboratory experiments to determine
the dynamics of movement of a sugar solution in vessels connected in
series. Described are the experimental techniques and the results
obtained.
Card 1/1

YAROVENKO) V. L.
YAROVENKO, V. L. "A Continuous Method of Fermentation in the Production of
Alcohol from Raw Starch-" Min Higher Education USSR.
Leningrad Technological Inst of the Food Industr7. Leningrad..
1956. (Dissertation for the Degree of Candidate in Technical
Science)
So: Knizhnaya Letopis', No. 19, 1956.

Chi
W.,~-.-Iter the InC vat 's 11,C0111 kf-j Inr Iferilizatwa. Irart
NV
-f n,l L! hiicd
2,,,.,~ v~t

YARO
Flenary session of the scientific couxcil of the All-UjLiox Scientific
Research Inatituts of the Alcohol Ixdustr3r. Spirt.prom.22 xo.1:46 156.
(DioUlling imaustries) (HIBA 9:7)
E

r
'!r'h!'aCiildltYUf flushes atcontInuous fermentation, V.
ax ~ u. o. Spirlowya Pion;. 22, No. 2,
Sirapfii-U 2 L ea,!h of barley jwash were disinfected and
sterilized and wexe kept for 0, 5, 10, 15, 20, 25, and 30 hn,
wort and 5:3 tril. of plant yeast. Curves are prmutcd for
the acidity as fowid from 0 to 14.1 lirs. of fermentation.
The acidities found tanye from 0,2 to 1.7*, they increase
with increasing ftrineutation time, and tle samples of mash.
preparation of
whoriginally were kept longer prior to the
the fermentation mLxt., gave always hightr acidities at any
tirg!~.ofsampl withdrawal. Werner J,~c2bsnrl

I'=--t;'tA6SU TAt4 W'*b W-Ort 14 A C40M-

AddiA
to U
R
C4
695
Th
S
5
.
.
.
t:
.
.
.
,
fermartlag fiquid mav i~s frow wat to va',U~ciu!& d "I cx-
cm-'s premure maintain ~d at the iwLkd Vm. CC~ kicil"d f "ryl
tile
rCceffing Vat is fo I to file Iwad vat at a ImAut 1"~rv the
f
)eye of tile tutle throu C% which the feru euting liquid 0"

USSR/General Problems. Methodology. History. ~3cientific A
Institutions and Conferences. Instruction.
Q,uestions Concerning Eibliography and Scien-
tific Documentation
Abs Jour Ref Zhur-IMimiya, 1-10 3, 1958, 6830
Author V. B. Fremell and 11. L. Yarovenko
Inst All-Union Scientific ;~~,esearch Institute of
Alcohol and Liqueur-Vodka Industry
Title 71ork of All-Union Scientific Research Insti-
tute of Alcohol and L.*Lqueur-Vodka Industry
Orir,- Pub Spirt. prom-st', 1957, No 7, 18-24
Abstract To the 40th-anniversary of the Great October
Socialist Revolution.
Card 1/1

I'duary [of the USSRI for JOS' V. L. Varovesikv), SO,(!
23 Nio 1 4 im,717 9,~ 7
'7' Prom
.
jw-tt"'; At, vt "t

0 .1
p"'verrieut t'f rvaLm!", I trio: oblummy
ill plotcolytic wid alylylolytic rnzvwirq ill Otv
ft-If th~- ICUIE ~r4-parat;-'I-; r.-.i iliv tll.~ :.ctivit" (1 0!,
I
it"ut-ra"at
(d tv

TAR VNED, V. L.
t sessiod of the Scientific Council of the All-Union Scientific-
Research Institute of'the Alcohol Industry. Spirt. Prom. 23 no.2:
(XLRA 10:4)
(Distilling indbastries)

YARNORW9
J~ jv
scientific Research Institute of Fermentation Indnatrias in Poland.
Spirt. prom. 23 ne.4:44-46 '37 (MIRA 10;5)
(Poland--Distilling Indmetri"

YAROVMO, V.%
Acotone-butyl industry of the Polish People's Impublic. Spirt, prom.
23 no,5-.14-19 157. (RT31A 10:8)
1. Vaesoyusny7 muchno-tracleacvatallskly institut spirtovoy pro-
v7shler-nosti,
(Polan(I-Acotone) (Poland-Butyl alcohol)

FRMLI, Y.B.; YAR
Work of the All-Union Scientific Research Institut of the
Alcohol, Liqueur and Vodka Industry. Spirt.prom. 23 no-7:
18-24 '57. (MIRA 11:1)
(Distilling industries)

V
AR~Vli~! Vt.
TAROVZNKO-;'V.L.; KOMAROV, A.F.
Processing beat molasses at alochol plants in Czechoslovakia.
Spirt.prom. 23 no.8:25-29 157. (MIRA 11:1)
(Czachoilovskia--Alcohol)
fin

TAROVSHKO, Viktor Livovich; KUZNFTSOV, N.M., retBenzent; MALCHMIKO, A.L.,
ape.t-sr-sd.`-,'-"KOTALITWATA, A.I., red.; TARASOVA, N.M., tekhn.red.
[Continuous alcohol fermentation] Potochnyl metod apirtovogo
brotheniia. Koskva, Pishchepromizdat, 1958. 127 P. WRA iz-.4)
(Fermentation)

YAROVENN, II.L.; SKALKINA, Ye.P.,, PYKPOVA, S.V.; LAZAREVA, A.N.
Continuous fermentation. Trudy TSNIISP no.6:3-8 '.5P,. (JAIRA 14:12)
(Fermentation)

YAROVENKO, V.L.; SKALKINA, Ye.P.; PYKHOVA, S.V.; LAZAREVA, A.N.
Cyclic semi-continuous fernzentation. Trudy T-q4I!SF no.6:9-14 'f8.
(YJR,,' 14-:12)
(Fermentation)

YRR V F-1V i~ 6
KOKAROV, A.F.; YARO 1.0, V. L..
Power engineering and mechanization in alcohol plants in
Czechoslovakia. Spirt. prom. 24 no.1:17-23 158. (MIRA 110)
(CzechoslovWm-Distilling industries)

JAROTENKO, Y.L.; NAKHIWIOVICH, B,M.; SHCHEBLYKINA, U,A.; SHCHEBLYKIN, N.P.
Analysis of the battery method of fermenting in the manufacture of
butyl alcohol and acetone. SpIrt. prom. 24 no.5:5-11 158-
(Butyl alcohol) (Acetone) (MIRA 11:9)
-T~

YAROVENKO, V.L.; MAMMA, A.U.
-- ----- Z:- ------------
Sterilization of the fermentation battery for the production of
alcohol from molanses. Spirt. prom. 24 no.6:10-13 '58.,
(Formontation) (141RA 11:10)

~/ L
..4.8
TIVIAO Ca timovs rersantation end sro*dtxc of
trozhonlys I vyrmohohI,m-tyo atkrearg-Alsoov)
TMOVICAM re.talk Akadesil muk SIM, 1959v Ir 2o Vp 106-109 (905R)
Alamo?. The lnotttut aikrobtologil kk&4~mil each 5531 (Microbiological
Institute of the Acadom;r of Sciences, USSR) coft-u~4 .
act.--* from October 13 to 15, 1950 which dealt ith the
la,vot1gttaft at moss warkime results to this field as oil
with th. at . further Intensification of the
production. basing on Ile activity of storcorgantias. The
a wre then 200 representatives of
M..ia ft ranch research institutest enterprises,
so.aarkhox.., univer.itle., a. .011 an foreign scientists. The
f.1l.-i.6 lectures a.- board.
1. D. ly.ru-jimakly slake of the theoretical foundattom, or the
4 of contirmous alaroto breeding anA Its proopects of
1h
1Z4ation to the .1croUaloglo.l. Ialumtr7.
:;V
Is . A. Fl.,aka, Tatmays"I InsiLtut
Card 1/4 khltbopek-rmy provy-hloccoatt (All-Volas Scientific It .... ro h
Institute of Irvad-Fraiuattan Industry) dealt with the problea
of the brooding of yeast in sol.J104, Opt.Wag &also&*#.
T. A
Ad A P K chkors, vessay"A5 M-OK y
r
*
In Ak
~
A.11,cay I aultfitnO-spirtmy FroaYshl.nmeatt
Z All-Union Scientific 1.06%rah lustituto for the industry of,
Sydrolyals and Sulflto Spirits) evaluated the theoretical and
practical work In the field of continuous fermentation of "ad
hyd=l"&t-a and ulfits liquor as ..It to their utilization
for obtaining fodder yeast.
YA-J~JIAZOALOTI, Krasooyarokly g1drollsayy savad (Krasnoyarsk
Hyd"Iyols plant) said that the Introduction and conpletion of
the 4011%lOwum process at I ... I %rs-4ing made it possible to
Increase the output of yeast factories by too time.
-1-L-Zamm"dw A. L. Xalaboako, vaeftyumm" "Whoo-
-
re-GTO-do"Sal-ekly I"-TtVU-.
yT-.T*woy I Itherl-ecdahne, i
promwamosmooti (All-union Scientific loseartb Jaells%1to of
the Spirit, Uquour and Dra"y laftetr7), T. M. Nakhmasoviak,
Pokshuslashats laboratarlys,
(Deksheal sob silk Isleatifle ImseGrolk Labovetsfy) reported *a the
card 2/4 Xperimmiat at applying the aat%*& at Goatinews, foreentotlos

Coftf~* F--ti-o wW Broodlex of k"roarsaMs.s WT13O-5qt2-AAOO
of the starchy raw material &Ad symp to the alcohol and
scatome-hateml Industry. ' I
S. A. Kono low. All-Union logestiflo Research Institute of
-'tbi Alcohol, Liqueur and brandy Industry reported an 0*
problem of antiseptics In fightlus Inf.o%lou it" to ferments.
It tot s4krobt.I.Ctl kkadwati. "uh, USSS
Institute 4 f the L3 Ukr33R) report*& a& the
Investigation of the morphological and physiological
properties of reset.
A. Andrvaheyelgil spirtovoy sewed (Andmabovka
!'*Io.ylskovskiy spirtower 26764
Itaxtrow., raolehaq
(M'
so
Inark. 5"Jonok So-khos) "parted on so* working
results obtained by distilleries In the syrup fermentation by
using the method of continuous flow.
Lonifteradakiy univ.1.11ot (lArAngred,
vrA~Qrsitj).,:har%*%.rIzsd tL* correlation of reproduction
pvo~-. and bl..h..Lcal activity of ... tic mid bacteria let
the high-speed production of vinadar.
N. W. 14"BOTap Microbiological Institute of the AS U331
-1j; a ~ottho 'possibillty of obtaining vitamin a,, by
continuous brooding of proplonle sold bacteria
(propionavoklolyyo baktoril). S. L. PrInborgl O~Z~axAhaxmksjaj
Tossayusnyy
(111-Unios, Scientific Ro"amb Institute of Antiblati*e)
"ported an the applic4tion, of this method to %be production
of penicillin.
111-Unloo, ScisAtiflo Research Institute of tha
and brandy Industry showed that the se,%hod of
somi.coutinuous treating of the fur4ru. A.prgtlluo Rigor
"Golorstes formatatIM 1. 1. Porfitlye,, laingr.d
University report*& an the results of Inveattlatious at the
natural microtlers, Wy the oetha& of capillary alaroo4opy which
he had developed.
1"-Kardpwa, Kirov University domeastrolod his me. hatcher
-I;r continuous brooding of microorganisms In laboratory
practise.
Lott and j;ssaboolovakla) exproo"d their
129
opWons a a the methods of o2stimmons brooding of micro.
this Ossforoodo It was potato& to the 040sesity of
:rCaniming the Ir us trial production of oulturso tar
Card 44 jotimmous form t.ti.16 a

TAROVENKO, V.L.; SKALKINA, Te.P.; FMIOVA, S-V. ; LAZAFJWA., A.N.
Xxperience in introducing and developing the continuous method
of fermentation in the processing of starchy raw materials.
Trudy TSNIISP no-7:3-16 159. (MIRA 13:9)
(Fermentation) (Alcohol)

SIALKINA, Ye.P.; TAROVOKO, V.L.; PMOVA, S-V-; LAZAUVA, A.N.
Multiplication of yeast cells and their distribution in the
battery in a continuous fermentation process. Trad7 TENJISP
n0.7-.16-23 159, (MIRA 13:9)
(Teast) (Fermentation)

PYKHCfVA, S-V.; YAROVMO, V-L.; SKAM&A, Ye.P.; LAZAMVA, A.N.
Use of the other - aldehyde fraction as an antiseptic in the
manufacture of alcohol* Trud~r TSNIISP no.7t25-28 159 iMIRL 13:9)
(Alcohol) (Antiseptice)

-YAROVENK09 V.L.; KO.PYLOVAg A,,M.
Improved design of a pump for transferring beer, Trudy TSNIISP
no. 8:157-164 159. (MIRA 14:1)
(Distilling industries-Equipment and supplies)
(Puinping machinery)

YAROVEITKO, V..L.
All-Union Scientific Research Institute of the Alcohol, Liqneur
and Vodka Industries and the 2lat Congress of the CPSU. Spirt.
prom. 25 no.1:15-16 '59. (MIRA 12:2)
(Distilling industries)

TAROVENKO. V.L,
New trends in the scientific research of the All-Union Scientific
Research Institute of the Alcohol Industry. bpirt. prom. 25 no.6;11-15
159. (MIRA 12:12)
(Distilling industries--Equipment and supplies)

KDBUALOV, S.A.; YAR VANKO. V.L.;_~!U~VA, X.Y.; BOROIKINA, V.V.
Disinfection of green malt. Spirt.From. 26 w.1.,13-16
16o. I (MLU 13:6)
(Malt--Disinfection)

TAROVIMO, V.L.; SKA IML, To.P.; FrKEK)TA, S.T.
Combined processing of potatoes into alcohol and starcb.
Spirit.prom. 26 no.4:4-7 160. (MM 13:8)
(Potatoes) (Alcohol) (Starch)

YAROVEKKO, T.L.
Method of contimouB fermentation. Spirt.prom. 26
no,5:3-10 160. (MIRA 13:7)
(Yermentation)

YAROVMMO. V.L.: WWROVICH, B.M.; SMUMICH, V.V.
Theor7 of the continuous acetone butyl alcohol fermentation.
Spirt.prom. 26 no.6:6-9 160. (MIRA 13:11)
(Fermentation)

YAROVENKOI V.L.j IIAKIDIANOVICHp B.M.; SHCHEBLYKIN, N.P.; SENKIEVICIlp V.V.
Study of continuous acetone-butyl fomentation caused by
Clostridium acetobutylimm, Mikrobiologiia 29 no, 41581-586
Jl-Ag 160. (MIRA 13:10)
1, Voesoyuznyy nauchno-isoledovatellskiy institut spirtovoy
promyshlennosti.
(CLOSTRIDIUM ACETOBUTYLICUM)

YAROVENKO, V. L.
Seco3;d International Syj~posium on ContinuouB Culture of Micro-
Organiaw. Spirt. prom. 28 no.S.*13-26 162.
(MIRA 16:1)
le TSentral'My nauchno-issladavatelinkiy institut opirtcvc7
promyshlennosti.
(Fermentation), (Microbiologya-Congresses)
4-Lk

YAROVENKO, V.L.; TIAKHMANOVICH, B.M.; SENKEVICH, V.V.; SHCHEBLYKIII, N.P.
Continuous acetone-butyl fermentation with an extended battery
charging cycle. Izv.vys.ucheb.zav.; pishch.tekh. 2:98-104 162.
(KRA 15:5)
1. TSentralInyy nauchno-issledovatellskiy institut spirtovoy i
likerovodochnoy promyshlennosti.
(Fermentation) (Acetone) (Butyl)
-77 `777M

DANILOV., K.G.; YAROVENKO, V,L.
Comparing the simplest mocUficatlons of the top part of fermenta-
tion batteries. Spirt.prom, 29 no.4:8-14 163s (MIRA IW)
1. Universitet druzhby narodp4 (for Danilov). 2. Vsesoyuznyy
nauchno-issledovatellskiy inbtitut fermentnoy i spirtovoy
promyshlennosti (for Yarovenko).
(Fermentation-Equipment and supplies)

YAROVENKO, VA.; USTINNIKOV, B.A.; FYKHOVA, S.V LAZAREVA,'
Testing and improvement of the technological flow sheet for the
combined processing of potatoes to starch and alcohol in the
Michurinsk Distillery. Trudy I'MISP no.l2t46-50 '62.
(RIRA 170)
. . . . . . . . . . . .

-MOVE -,V-L.; USTINNIKOV, B.A.; PYKHOVA, S.V.; IAZAREVA, A.N.;
NKO
KUCHEROVAY E.A..,
Utilization of the cellular Juice of potatoes in the combined
production of starch and alcohol. Trudy TSNIISP no. 13:3-10
t62. (MM 17 - 5)

YAROVERKO, V.L.
Baslo tasks of maientifie researah in the fermentation and
distilling industries. Form i spirt, prom, 30 no*30-6 164,
(MMA 18 2)
1. Vessoyusnyy nauahno-insladovatellakiy, inatitut fermentnoy i
spirtovoy prowfahlennostio

YAROVENKOIJ.L.; FYKHOVA, S.V.; USTINNIKOV, B.A.; LAZAREVA, A.N.; MAKEYEV, D.M.
Fementative hydrolysis of starch in continuous alcohol fe-mentat-ALOn.
Ferm.i Epirt.prom. 31 no.1:5-10 165.
(MIRA 18:5)
1. Vsesoyuznyy nauchno-issledovatel'skiy institut fermentnoy i
spirtovoy proWshlennosti.

YARMNKO V.L.; IJSTIMJIKOV, B.A.; LEVCHIK, A.P.; NECHIPORLWO, A.A.
Processing of sugar beets in a mixture witb grain and potato raw
materials and molasses. Ferm. i spirt. prom. 31 no.6:37-40- 165.
(MIRA 18:9)
1. Vsesoyuznyy nauchno-issledoltatellskiy institut fermentnoy
i spirtovoy prouWshlennosti (for Yarovenko, Ustinnikov).
2. 14ichurinskiy spirtozavod (for Levchik, Nechiporenka).
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