SCIENTIFIC ABSTRACT KARAULOV, V.M. - KARAUSTYAN, T.V.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R000720620018-5
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: June 13, 2000
• Sequence Number: 18
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

L 33228-66
ACC NRt -AP6024588 SOURCE GUM: UH/U314/66/LX-)UIUVJ/UL7/-'I'/C)029
AUTHOR; Karaulov, V. M. (Engineer); Selivanov, A. N., (Engineer)
OR6: none
TITLE: Results of tests on shock-cavitation colloidal mills
SOURCE: KhiaLcheskoye i neftyanoye mashinostroyeniye, no. 3, 1966, 27-29
~.TOPIG TAGS: colloid chemistry, cavitation, electric motor, production engineering,
chemical dispersion, colloidal mill/L-.202 colloidal mill, L-808 colloidal mill
ABSTRACT: The itAicle presents foz7aCLas for calculating productivity and
cap,-3,city of electric motor& of shock-cavitation colloidal mi.11B. The
fomau,16a aro derived from rosulto of touts of the mills L-202 and L-009
produccd by the Deutsch Vakuumapparat Companyy conductcd at the Tambov
i 4uil1ino Dyo Plardt. The mills IP-202 and L-808 have several deficionciesp
r
restricting their extensive use in dispersion of Ln~si~one! The most
oub3tantial deficiencies discovered during the testing -are: r pid wear
of .-otor striking pins in proces3ing suspensions) overheatingi rapid wear'
of bearingsp low capacity of electric motors.. overheating of suspensions
in the process of dispersion and excessive foaming. Orig. art. has: 4' formulas
and 1 table. [JIPRS: 35,728)
SUB COUE: 07, 14 SUBM DATE: none / ORIG REF: 001
C I !/,-t
C
arl-

KARAULOV, YO.V.., kand.arkhit?ktury
Architectural design features of the brick walls'of buildings~in
Moscow at the end of the 18th and beginning of the 19th century.
Mat. po'ist. stroi. tekh. no.2:181-213 162. (MIRA 16:5)
- (Moscow--Brick walls)

COUNTRY % USSR
i : GuIltivated Plwits - ?otatoos, Vegotublea, lvucurbit3.
1
Ne.14, 15"58, Nl,%.63416
4"!
AUT11GIR Lleksandrov, 5. V. , Karaulova
V
~a i on
A.11-Union In8tituta f rit Cult I
T-Ir IIII-E
New Method of 3rowinlo To.,u, tons in Hothousq i.
Sad i ogorod, -2957, No. 12, 12-15
A ~i;3 C T !a 1956, an experiment on growi-n- tomatoes in bottomless
cylindrical vessels (made of Saw-ld asbestos-cament tubes
14.5 em In dianieter and 20 am in haight placed on slal-)
was carried out at VIR find the labonttory, of Lertin,-rald
hothouste-hotbed oombine. Me vessels were filled to 2/3
with a L,~Ixture of humus and turf soil, wid tome-to seedli-ags!
of the variety Loningrad.skiy okorospelyy aged 20 days wero i
sot out. Slag was wetted daily with water. Once a we5k,
thq plants were fed with a sblutJon of mineral fart-ilizers.
In tho firat month of frult bearing, a yield of 4.65 kg
from 1 M2 Vas gathered (33% more than with the cultivation
-ard: 1/2

KARAULOVA, L.P.
Continuous production of yeasts. Spirt.prom. 27 no-4:34 161.
OIIPJ~ 14:6)
(Bi3,sk-Yeast)

XMMOVA p IM.
NIMES AND BURSOG
Popov family. lied. sestra. no. 4, 1952.
Monthay List of Russian Accessions. Library of Congress. November, 1952. Unclassified.

KARAULOVA, M'.
Nurseig and Nursing
Nurse A.D. Petrova. Med. sestra No. 9, 1952.
Monthlr List of Russian ACceSsions, Tibrary of Con,--rose, December 195Z. Unclassified.

KARAULOVA, N.A. (Moscow).
Faultless worker. Ked.sestra no.7:27-28 JI '53, (KLHA 6:7)
(Nurses anci nursing)

YARAUWVA, M.L. (MOSCOW).
Wortby example. Med.sestra 110-7:28 Jl 153 (MLRA 6:7)
iNursea and nursing)

EARAULOVA, M.A. (Moscow).
Polina Fedorovna Chernykh. Med.seatra no.12:29 D 153. (M12A 6:12)
(Chernykh, Polina Fedorovna)

tekhn.
VIDINEYEV, Yu.D.; BALAKIN, A.Ya., inzb.; ~A
Wire dynamometer for reinforcement wire. Bet. i zhel.-bet. 8
no-3:126-127 Mr 162. (MIRA 15:3)
(Dynamometer) (Concrete reinforcement)

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leo iA 0
ON-,- e,
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USSR/Chemistry - Nicotine Tan 1948
Chemistry - Amino Derivatives
,0
.-t
"Amino Derivatives of Metanicotine," Ya. L. Gclld-
farb, Ye. N. X!%rauloya, Inst of Org Chem, Aced Sol.
USSR, Moscow, 61 pp
*Zbur Obahch Xhim" Vol ME= (TXXX), No I
Mole for mole acetylizatlan of alpha-amincmetanloo-
tine with acetic anhydride results in acetyl pro-
duced alp'ha-minometanicotine. Alkali when acting
upon iodomethyl alpha-aminametanicot,ine produces
trlmetbyl and alpha--i-o-(beft-butadenul)-IWridine.
When alpha-minometanicotine In hydrated In the
presence of Pt/PtO2 according to Adam's methcod, me
mole of hydrogen Is absorbed resulting In obtaining
alPha-aminodihyd.rometanicatine. Submitted 13 Dec
1946.
64T46

----Www,;Wwww .1 a awe W* 0 a w 00000 W-WT~-
- WIVIT role t Ollf! 6069 o:-
0-41 ftfpPiAittilitt fill is W NO It 41 U If *'to
~k r ik it r 11.
($041 1t -:11--, 1-00
Sol, AWO 010PImst MI s
go AMM IIJOA~dss od tha pysidbia series, Yt. L. GoI'd-
farb ant) R, Ksrut.tluva. P,41ady Akad. Naish S.S,-
00 S.R. 63. cf. C.A. 42, ULM. -Among the
of Ibe reaction ID! Ac.0 with a- anti a'-arninu- -00
we products of fin which are muigned
the v 09
structum C1101201INII.Iff
and resp, I-be
:a I structures are confinned by osual"tion. OAvitisation of -*4
the At dvriv., " .3.CAI.N(Nll,ICII-CIICIIsClt,N%IeAc, "as
in 15% HCI pye tl~ 9U, (front -00
e0 CA); ]/Cf sell. W. IOD-70.5, (from Moll) . pkemyl-
0 h*asm, tn. 202-3* (from RtOll); jemwarWsoms, sea
as .3 decornp. 218'; aximr, in. 1&3.5* (from water). This zoo
aldtbrde with ArTO pim a momo-At dorm, rn.
ago Matu CJW- Cloulution of '-aminoractanimfine in
99-3 t5% IICI gave 2.3-CAMNIMC110, m. lGI' (on pse-
heated block; on slow beating the product does not m.
00%, even at 450*); IICI =D,decom~. 2M-10 (froin FtOli); roe
004 decomp. 232 (front EtOll); se,"i- =a
=i`ad=-P. =M (from water); arime, m. 217-
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A I M. S LAITALLURGICAL LITINATURI CL&SWICATION
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0 0 0 0 0 * 0 0 0 0 0 a a 0 0 a a 0 4 6 Ilk 0
0 00 0m a `0 0 a a 0 a* a a 0 0 a 0 0 e(

X&RAULOVA, Te.N.; GALIPM, G.D.
2b4-W:
Gonversion of P-bromoethylphanyl other in the presence of zinc
chloride and mixtures of zinc chloride and aluminum chloride.
I2v.AN SSSR.Dtd.khim.nauk no.5:949-950 3-0 155. (HIJIA 9:1)
1.1natitnt orgamicheakov khinii imeni B.D.Zolinakogo Akademii
nank SSSR. (Bronoethyl I*enyl other)

AID P 3754
Subject USSR/Chemistry
Card 1/-1 Pub. 152 - 18/22
Authors : Karaulova, Ye. N. and A. S. Nekrasov
Title! : Synthesis of dibenzyl sulfide
Periodical Zhur. prikl. khim.-.28, 9, 1012-101-1,, 1955
Abstract The synthesis of dibenzyl sulfide from benzyl chloride
and sodium sulfide with a yield of 93% is described in
detail. This method may also be us~_d for the prepara-
tion of alkyl- and aralkyl sulfides. Four references,
none Russian.
Institution : None
Submitted : Mr 12, 1954

KAPLAULOVA, Ye.11.;-GALIPERS, G.D.
Oxidation of sulfides with hydrogen neroxide. rhim.i tekh.topl.no.g:
39-44 S '56. 'kMLR.A 9:10)
1.1natitut nefti Alcndemii nauk SSSR.
(Sulphides) (Hydrogen i)eroxide)

AUTHORS: Karaulova,. Ye. N. , Moylunova., D. Sh. , 791-11-27/56
-Gallpern, . .
TITLE: On the Therinal Isomerization of Alljlarylsulf ides
(0 termicheskoy izomerizatsii aililariloullfidov).
PERIODICAL: Zhurnal Obshchey Khimii, 1957, Vol. 27, Nr 11, I)p. 30~"A-3040
(USSR)
ABSTRACT: According to Claisen the characteristic property of the
allylaryl-esters is the so-called reerouping, the ability
of isomerizing into o-allylphenols on heatint-. It was
attempted to a-pply the thermal isomerization to the sulfur-
analoeues of these esters, to allylphen5,lsulfide and o-
and p-allyltolylsulfide. In contrast to the results obtained
by Hurds and GreenGards it was found that on heating
(boiline) of allylDhen-;lsulfide without solvents no
allylthiophenol is to ~e obtained, but onl-, propenylphenyl-
sulfide which, if heated, 3fields concentration products. The
structure of the Droduct obtained in the thermal
isomerization of allylphenylsulfide was determined by
hydrogenation over nickel. Thuq this iaonerization -.-ijth
C,ird 1/2 subsequent formation of allylthiophenols (Claisenian

~7 9_ 1
On the Thermal Isom-erization of illlylarylf~ulfidL,3 1 1-27/56
reg.roupint7), like -:n the analo,_ous ox~-.ven compounds, has no
effect. In thernal i3omerization the thylaryisulf ides are
converted to the correspondinE proj)(!nylarylsulf ides. At
first they obtained allyl-o-tol.vlsulfide, allyl-o-tolyl-
sulfone, prODehyl-0- and p-tolylsulfides, propenyl-o-
tolylsulfone, cis- and trans-propeiylphonyl-3ul~lones. Allyl-
phenylsulfide and propenylphenylsulfide are split up by the
solution of mercuric chloride in alcohol, on Y.-hich occasion
mercuric chloride of thiophenol forms.
There are I fifure, and 121 references, 2 of which are
Slavic.
ASSOCIATION: Petroleum Institute AS USSR (Institut ne'Lti Akaademii nauk
3SSR) .
S'UBMITTED: December 10, 10,506
AVAILABLE: Library of Con6ress
Card 2/2 1. Allylarysulf ides - Isomerism

AUTHORi KARAULOVA,Ye.N., MEYLANOVA,D.Sh. 20-"6-26159

TIT-LEt GALIPEHB,G.D.
On KLEISENs Rearrangenment in the Allylarylsulphide Series.
(0 peregruppirovke Klayzena v ryadu allilarilsullfidov, Russian)
PERIODICALt Doklady Akademii Nauk SSSR, 1957, Vol 113, Nr 6, pp 1280 - 1282
(U.S.S.R.)
ABSTRACTt This rearrangement is an isomerization which, according to the
opinion of some scientists, is characteristic not only of the
allylarylethers but also of their analogya. In contrast to Hurd
and Greengard the authors found that in the case of boiling of
allylphenylsulphide without solvent practically no allylthiophenol
is formed, but an isomerization of the former in propenylphenyl-
sulphide occurs. It is identical with the product insulated by
Tarbell and Mc Call which they obtained by the action of sodium
alcoholate in an alcoholic solution on allylphcnyloulphide. When
standing or warming propenylphenylsulphide forr~s condensation
products. The thermal isomerization of the allylarylaulphides
develops according to the scheme:
to ~ ArSCH - CHCH
ArS - CH
CH - CH
1 0-C
, (Ar - C
H
CH
H
2
2
6
6
3
4
5
3
and n-C 6H4CH 3)
Furhtermore, the single reactions with yields and experimental
Card 1/2

2o-6-26/59
On KLEISEN's Rearrangement in the AllylarylBulphide Series.
ASSOCIATION:
PRESENTED BY:
SUBMITTED., -
AVAILABLEt
conditions are described in detail. A colored reaction with
sulphuric aGid is characteristic of the here investigated
propenylarylsulphides: A red coloring results, which quickly changes
into brown. In contrast to this, allylarylsulphides, after addition
of concentrated H 2s0 4~ turn only faint yellow. The obtained results
allow the conclusion hat KLEISEN's rearrangement does not take
place in the case of the allylarylthioethers, in contrast to
corresponding oxygen-compounds. Allylarylthioethers isomerize
in the case of heating in corresponding propenylarylsulphides.
(1 Slavic reference).
Petroleum Institute of the Academy of Science of the U.S.S.R.
A.V.Topchiyev, 11ileraber of the Academy
24.12-1956
Library of Congress
Card 2/2

11(4) PHASE I BOOK EX?T~OITATIO'N 3 Oil/l -7
Aka-demiya nauk SSSR. Institut nauchnoy informatsil
Xhimiya nefti i gaza (Chemistry of Petroleum and Gas) Moscow, Izd-vo
AN SSSRI 1958. 477 P. (Series; Itogi nauki; Itimichefkiye naul-A,
2) Errata slip inserted. 3,000 coPles printed.
Ed.; G.D. Gallpern, Doctor of Chemical Sciences; Ed. of Publiching
House: I.P. Lookutova; Tech. Ed.: Ye. V. Makunl*
PURPOSE: This Wok is Intended for the special~:3t worl,,IML in the
field of oetroleum chemistry and for the orf-~iLntc cherai,,t In
related fields,
COVEMAQEi This is the first volume of the z1orloo 0,.,votocl to 1-'h~,
gvpros inade in I)Qtroleum and frv.~3 (flioraistry. Tht~ Clrolk-' rr, of 11-hlf~
collectioti oontaiiif-) survey ;,irtit"Ic-t-1 cl'ml~)Iled by the ataff ril, the-
Petroleum Institute, AS USSR. Vic: authorr, are
on methods for the isolation, separation, an(! Ide-nt'Mcat--I on of
5111fur organio 00japovindo In Petroleum. Tho avtlojot) g1ve 11 flurvoy
oard 1/6

Chemistry of Petroleum and Gas (Cont.) SOV/1785
of literature up to 1956 with some coverage of recent research up
to 1958. The second part is c�ncerned with the characteristics of
high molecular weight compounds and methods for the study of their
composition.. There are 124 references.
TABLE OF CONTENTS:
From the tditor 5
PART I. THE CHEMICAL COMPOSITION OF.THE SULFUR COMPONENTS
IN PETROLEUM AND MET HODS FOR ANALYZING THEM
Luklyanitsa, V.G. Methods for the Analysis of Sulfur Compounds in
Petroleum and Petroleum Products 13
This article reviews the literature on qualitative and
quantitative analysis of sulfur organic compounds in
petroleum, on problems dealing with the elementary functional,
group, and systematic analysis of sulfur-containing petroleum
products, and on methods used in the analysis of sulfuric acid,
The author includes tables for the comparison of prqcedures
Card 2/6

Chemistry of Petroleum and Gas (Cont.) SOV/1785
for the systematic analysis of complex mixtures containing
all possible groups of sulfur organic compounds. Special
attention is given to modern electrochemical analytical
methods in nonaqueous media. There are 18 tables and 582
references, 134 of whieh are Soviet.
Sergiyenko, S.R.,, and V.N. Perchenko. Study of the Chemical
Structure of Sulfur Organic Compounds in Petroleum by Means
of Catalytic Hydrogenation 113
The authors review papers on the methods for the hydrogenation
of sulfur organic compounds. The method of catalytic hydro-
genation promises to be very effective in the study of the
structure of sulfur organic compounds. There are 9 tables
and 29 references, 11 of which are Soviet, 3 English,
4 German, and 1 French.
Karaulova, Ye.N. Oxidation of Sulfur Compounds 130
This review article fills a gap in literature surveys.
Card 3/6

Chemistry of Petroleum and Gas (Cont.) SOV/1785
It presents systematically the experimental research on
oxidation methods for the separation of the sulfur compounds
in petroleum. The author includes comparative tables for
groups of compounds and for oxidizers used. There are 3
tables and 136 references, 20 of which are Soviet, 77
English, 26 German, 10 French, 2 Italian, and 1 Dutch.
PART II. HIGH MOLECULAR WEIGHT COMPOUNDS OF PETROLEUM
Sergiyenko, S.R. High Molecular Weight Compounds of Petroleum 199
This review covers the study of the composition of high-
boiling petroleum fractions. It includes much of the
author's own research. Several of the points are debatable
and the classification of organic compounds into one large
group of "hybrids" is regarded by the editor as improper.
A-problem which has not yet been solved, namely, the
relationship between monomers and polymers in * crudes
is also treated. It is assumed that there are two basic
types of polymers in crudes: the primary and the secondary
polymers, N.D. Zelinskiy and K.P. Lavrovskiy indicated
Card 4 /6

Chemistry of Petroleum and Gas (Cont.) SOV/1785
that steroids are postible primary compounds. In spite of
the view of A.F. Dobryanskiy, asphaltenes, carbeneso and
carboids are very often regarded as secondary polymeric
components of petroleum. Much space is given to cancerogenic
components of petroleum. There are 26 figures, 41 tables,
and 247 references, 120 of which are Soviet.
Smirnov, B.A. Use of Infrared Spectroscopy in the Study of the
Hydrocarbon Composition of Petroleum and Petroleum Products 414
The author reviews existing literature on infrared spectros-
copy in studies of the hydrocarbon composition in crudes
and petroleum products. He covers the spectral analysis
of Individual and group compositions, ranging from gases to
heavy oils. A description Is given of the possible use of
infrared spectroscopy in the analysis of high-boiling frac-
tions and in the classification of hydrocarbon types. There
are 81 references, 6 of which are Soviet
Card 5/6

50)
AUTHORS: K r.~ova'._Ye.' 111-eylanova, D. Sh. SOV/2o-123-1-26/56
Gallporn, G. D.
TITLE; Synthesis of 2-1.1ethyl- and 3-1~et~lyl-i-Thia-Indans and
2-Ethylthiaindene (Sintezz 2-10til- i 3-:71letil-1-tiaindn-ov
i 2-etiltiaindena)
PERIODICAL: Doklady Akadem-ii nau's' SSSR, 1950, Vol 123, Nr 1,
PP 99 - 101 (USSR)
ABSTRAXT: In connection with 'the investication of the sulfur-
containin,~' compounds of tho medium naphtha frixtions
so-called so-miaromatic sulfur connipounds are of inte--est.
Among them, particular attention deserve the alk.yl
derivatives of the 1-thia-indan (2,3-dihydro-thia-
naphthene) with substituents in a 5-membered ring. T,,,e
authors found, in seLrch for a synthesis.method for
such compounds, that the hitherto unknovm 2- and 3-
methyl-1-thia-indans (III) can be easily produced
by a gradual reduction of the sullf'ones (I) of t'ne
Card 1/3 corresponding 2- and 3-met-hyl-thia-indenes. A simple

SyntheF,iq of 2-Motilyl- and 3-Methyl-i-Thia-Indans and SOV/2o-123-1-26/1.6
2-Ethylthiaindene
method of synthesis of the 2-alkyl-thia-indenes
is the metallization of the thia-indene (thia-
na-Dhthene ) by n-butyl lithium with subsequent a1hy-lation
by dialkyl sulfatos. By the influence exerted by di-
methyl- and diethyl culfete upon 2-thia-indenyl lithium
the 2-methyl-thia-indene and the 2-etI~Yl-thia-indene
heretofore not described were obtained. The first
can be oxidized by hydrogen superoxide to form 2-
methyl-thia-indene sulfone (Ia). The structure of the
2-methyl-1-thia-indan (IIIa) was confirmed by a
synthesis according to the given sc-ene. Experimental
data (being not denoted as cuch), are following. There
are 6 references, 1 of which is Soviet.
ASSOCILTION: Institut nefti Akade-3ii nauk SSSR (Petroleum I-11stitute
of the Academy of Sciences) USSR)
PRESE!71ED: June 14, 1958, by A.V.Topchiyev, Academician
Card 2/3

O'.IPHPQAC CEVA-
A3mrrAfln4r.CKHX COEANUUMA BZ41U
r. a. r..... mms ...... P.
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Tin KWA*Ioysv COW*" fOr QMMSI WA AFPIW Clmk'MU7 30
soctics at Cb"kUU7 WA cuedcal Tochaalo~a 't 7.014,
"bl. Tij, Afta. 86l. tm, M"m I;wg
0-hakalad to W p"Mud at wom met gamod *me%".
avow, 23 mrvb Im.

KARALTLOVA ,I., OT301-l'-N1 TzV, R. L., G. L., AIVA.`W3 D.
-7-1 ~-115 14 -N IUKYANUOSA, V. G., EATMIKAYA, .1k. A., TD,,'I,~ V) V.
(SLCITIOt! V)
'lCorrpcsition of z~ulfur- 1,~itroCen-Or.~-anic Compoun,~S Cont2ined in
the Oil ofthe -'-astern Ar as in tl-e Loviet Union."
!"Leoc,,rt~Sulbl-,itted~~OiT'-.he :-'if th ',',or2d Petrolcur. Clongrcss, -')( ;ay -
19LQ iork.

TV V.
Ell
Mv V
Iva
(ell
61Y "Y

5 (3)
AUTHORS: Gol I dfarb, Ya. L. , Karw.~_'_ova, Ye. N. SOV/62-59-06-24/36
TITLE: On Some Esters of Thiolformic Acid (0 nekotorykh efirak1h
tiolmurav'inoy kisloty)
PERIODICAL: Izrestiya Akademii naiak SSSR. Otdeleniye khimicheakikh nauk..
1959, Nr 6, pp 1102 - !105 (USSR)
A13STRACT: The thiolesters are widely used in different industrial bri~nf_-.h-
es as intermediate products (Refs 1-11). The present investi-
gation was concerned with a detailed investigation of the for-
mic acid esters which -are of interest for these intermediate2
ani up till now scarcely described ~n publications. Thiolfor-
mic acid was produced by formylation of the sulfohydrile group
of the compound RSH by use of ar anhydride combination of foT--
mic- and acetic acid.
CH ----C - 0 0
3 1,-
0 r~ RSH -4 He (R . 0 H CH"; n-c 1199C H
6 5 4 2 5
0 Sn
Card 1/3 The anhydride forming reacts with its formylradical with hydro-

On Some Esters of Thiolformic Acid SOV/62-59-6-24/36
xyl containing compounds (Refs 14-17). on the basis of an ex-
ample, formylation of benzylmercaptan was carried out for the
purpose of avoiding a decomposition of the anhydride compound,
the reaction temperature was chosen in so low a range that no
separation of carbondioxide could take place. The benzylesteT
of the thiolformic acid (1) was obtained. The buthylester of
the thiolformic acid was under quite similar conditions als3
produced from buthyl- and ethylmercaptan with the anhydride
combination. Furthermore, it was shown that the trithiolformic
acid, by passing an intermediate stage, forms the esters of the
thiolformic acid. (I) reacted in the presence of hydrochloric
acid with benzylmercaptan under formation of the eater of the
orthotrithiolformic acid. The esters of the thiolformic acid
proved to serve as N-formylating agents. By the action of (1)
upon a-aminopyridine formyl-a-aminopyridine was obtainedi by
reacting with all thiolformates described here with pheny1hy-
drazine P-formylphenylhydrazine is formed. There are 20 ref-
erences, 2 of which are Soviet.
Card 2/3

On Some Esters of Thiolformic Acid SOV/62-59-6-24/36
ASSOCIATION: Institut organicheskoy khimii im. N. D. Zelinskogo Akademli
nauk SSSR (Institute of Organic Chemistry imepi N. D.
Zelinskiy of the Academy of Sciences, USSR)
SUBMITTED: September 11, 1957
Card 3/3

GALIPIRM, G.D.; KARAUWVA, Te.N.; NOVOZMLOVA. T.S.
Adsorption of sulfoxides from dilute solutions. Trudy Inst.nafti
13:51-57 159. (KMA 13: 12)
(Sulfoxide) (Ebrdrocarbons)

AUTHORS:
TITLE-
PERIOD'LCAL:
ABSTRACT:
Card 1/3
Karaulova, Ye. N., Meylanova, D. 3h,, SOV/79-29-2-63/71
Synthesis of 3-Methyl-l-Thiaindane and Regrouping of Allyl-
aryl Sulfones (Sintez 3-metil-l-tiaindana i peregruppirovkz.
allilarilsullfonov)
Zhurnal obahchey khimii, 1959, Vol 29, Nr 2, pp 662-666 (USSR)
Of topical interest is the synthesis of the so-called "semi-
aromatic" bicyclic compounds, as components of various mineral
oils, especially those of the homolo.-ues of 1-thiaindane, with
substituents in the hydrogenized ring. H. I. Backer and 11. Dost
(Ref 1) found that on heatinj allylphenyl sulfone with H 2 so 4Y
which contains boron fluoride, an isoinerization takes place
under formation of a product, to which the structure of
3-methyl- 2, 3-d ihydrot Ili onaphihene sulfone was ascribed- The
reduction of the sulfoxie group therein should lead to
3-methyl-1--thiaindane (3-methyl-2,3-dihydronaphthene). How-
ever, on reducing the 11cycloi-somerization product" of allyl-
phenyl sulfone, which was obtained accordinE to reference 1,
the authors found no 3-methyl-1-thiaindane, but propylphonyl

Synthesis of 3-1,1,ethyl-l-Thiaindane and RegroupinF SOV/79-29-2-63/7111
of Allylaryl Sulfones
sulfone, almost quantitatively~ Thus the compound assumed by
the above authors as being 3-methylthiaindane sulfone has no
bicyclic structure; the isomerization product of allylphenyl
sulfone was found to be a propenylphenyl aulfone, Likewise,
propenyl-n-tolyl sulfone forms on the action of H 2s04 in tile
presence of boron fluoride upon allyl-n-tolyl sulfone; on the
reduction with LWH 4 the latter is transformed into propyl-
-n-tolyl sulfone, Thus, on the action of H 2so4 upon allylaryl
sulfones no cyclization takes place under formation of
3-methyl-l-thiaindane sulfone. In this connection, allylaryl
sulfones isomerize immediately into propenyl compounds in the
way shown by schemelinreference 2. Further experiments showed
that the synthesis of 1-tbiaindanes by cyclization of allylaryl
sulfides and sulfones is not possible in E-ood yields. The
synthesis of 1-thiaindanes was also attempted over thiaindenes
(benzothiophenes) and their derivatives. 3-methyl-l-thiaindane
was obtained by the reduction of 3-metbylthiaindene sulfone
Card 2/3 (Scheme 2),, The structure of 3-methyl-l-thiaindane was

SynthesiB of 3-Methyl-l.-Thiaindane and Regrouping SOV/79-29-2-63/71
of Allylaryl Sulfones
ASSOCIATION:
SUBMITTED:
determined by hydrodesulphurization over nickel (Scheme 3).
The yield in 3-methyl-l-thiaindane amounts to 41 ',J, calcu-
lated for thiophenol. There are 10 references, 2 of which
are Soviet.
Institu'. nefti Akademii nauk SSSR (Petroleum Institute of
the Academy of Sciences, USSR)
December 4, 1957
Card 3/3

5(3~j SOV/79-29,-9-48/76
AUTHORS: Karaulova, Ye. N~, Gallpern, G. D.
TITLE: On the Reduction of Sulfc-xides
PERIODICAL: Zhurnal obshchey-khimiliq 10~511, V-,!- 29, Nr 0, PP 3033-3036
(USSA)
ABSTRACT: In the separation of the sulfides from petroleum dist1llalpes
as'sulfoxides (Ref 1) the authors had to find a uhiform. pre--
parative meth6d of regeneration of the sulfides from sulf-
oxides, which is of general interest but had hitherto not bepn
dealt with in publications. Prev-,ous reduotion experiments
of dibenzyl sulfoxide with du8t in acetic acid medium
failed; dibenzyl sulfide is formed in low yields in a mixturs
of acetic- and hydrochloric acid. From the publications it may
be seen that various ot-her methcds -f reducing sul-foxildea ar~j
not suited (Refs 2-11). In the preceding paper the sulfoxi4d-:::3
were reduced 1) with hydriodir ac.-,d,2) wit-h alurr~num llth.-um
hydride. D. Jerchel-, L. Dippelhoferv D. Renner showed tha'~
dialkyl sulfoxides with long chains may be quaiitat_fvely de-
termined by the reduction with potassium iodide in acid
medium. This method may, however, not be lised for a quanti-
Card 1/3 tative'determination of the sulfoxides (Ref 13). In this case

On the Reduction of Sulfoxides
S OV/7 9 - 2 9 - 5 - 486
it was found, however, that the effect of hydried-fic a,~id may b~
used in the preparative reduction mothod of sulfoxides to sul-
fides. in the reaction of diisoamyl-, dibenzyi--, diphEnyl-,
3-methyl-l-thiainclane sulfoxide with potas S4UM iodide in hydro-
chloric-acetic acid medium the corresponding sulfides are form-
ed in rather good yields. The separation of iodine in this re-
action may serve as qualitative reaction to the sulfoxides. The
presence of sulfides and aromatic 'hydrooarbcns in this case has
no disturbing effect; only fr. the presence of oxaldi,.~_,ng
which are capable of separating Jodine frcm potassi~im iodide
and from compounds which easily link iodine such as phenol% -(;n.-
saturated hydrocarbons etc this determination cannot be carri~_I
out. According to F. Braun ~Ref 14) `.-he alaminua, lithium hydr:Ae
was used as reducing agent of diisuamyl-, dibensyl-, diphenyl-,
3-metkyl-l-thiaindane sulfox-Ide in ether-benzene solution wiih
the corresponding sulfides resulting smozthly. The latter re-
duction method is to be preferred to thati, with !~yd--r-'odic aoid
since this acid may iodinate the 7eact-ion products. -The r,~-
diiction of the sulfoxides with al-an-Inum iit,~ium hyd-ride is nci-
Card 2/3 complete; however, the sulfoxide wh"Iolh at first did no,. oor.-

On the Reduction of Sulfoxides
50V/.719- 29-,9--,'B//7
pletely enter the reacti on mav 1,ji:. xedu~,ed onrue
more. There are 18 referencee, 5 of -e,,h".,,h are Sav2~Lit.
ASSOCIATION: Institut nefti Akcadpmii nal~k 3SSR (Pp-;-cleum of th,?
Academy of Sciences 'USSR)'
SUBMITTED: August 6, 1958
Card 3/3

50) 30'1/20-124-3-2r~/67
AUTFORS Karaulova, Ye. N., Gallpern, G. D.
TITLE: An Oxidation Mlethod for Separation of Sulfides From the "edium
Fraction of Petroleum (Okislitellnyy metod vydeleniaiya sullfidov
iz srednikh fraktsiy nefti)
PERIODICAL: Dokludy Akademii nauk SSSR, 19511, Vol 124, Nr 3, PI) 5,93-59~
(USSR)
ABSTRACT: Luklyanitsa and Gallpern (Ref 1) huve found t),;tt the ox.-Jdation
potential of organic sulfides into sulfoxides differc %irked-
ly froia that of the oxidation of hydrocarbons and of sulfur
compounds in other ~;roups. Consequently, there is a possibility
of a selective oxidation of the sulfides in the medium petro-
leum fraction. By an addition of glacial acetic acid and hydro-
gen superoxide it is possible to transform the sulfides
quantitatively into sulfoxides vithout affecting the hydro-
carbons themselves or the conpounds of the thiophene series.
Tile resultin- sulfoxides are out with Y.,Liter, the extract
is concentrated in the vacuum and treated wit1h c',.loroform.
The chloroform extract is dried b.-,, means of calcium chloride
,e1 the
and chromatographed on cilica gel. From the silica c,
Card 1/2 sulfoxides are re-extracted by means of -petroleum ether, benzene,,

S07/2o-124-3-25/67
An Oxidation M~ethod for Separation of Sulfideo From the Medium Fraction
u
of Petroleum
chloroform, and alcohol. ~_Ilhe elementary anal-~sis of the sulf-
oxides yields the general formulae C nH 2n-2 Sy nH2n--4 S and
Cn11 2n S. Their constitution has not yat be~*.,n invest~,,,ated. -
The oxidation met`iod proposed io of iri,,portance for Diesel oil
and medium petroleum dis-jillates,, as the sulfur is contijined
wainly in the form of sulfides, iheroas the ',,~,,drocarbons con-
sist Of difficultly oxidizable compounds. There are 3
and 5 Soviet references.
ASSOCIATION: Institut nefti Ak--ademii nauk SSSR (Petroleum Tnstitute of the
Academy of Sciences, USSR)
PRESENTED: July 29, 10138y by A. V. '2opchi-ev, licademician
SUBMITTED: July 29:, 1958
Card 2/2

LUKIYANITSA., V.G.; KARAULOVA Ye.N.; GALIFERN., G.D., doktor IdUmicheskikh
nauk j-~~
Study of sulfur compounds of petroleum in the Soviet Union.
Metod.anal.org.soed.nefti,ikh smes. i proizv. no.1:6-20 160.
(MIRA 14: 8)
(Petrole=~-Analyais) (Sulftw organic compounds)

KARAVLOVA, Ye.N.; GALIPEM, G.D., doktor khimicheakikh nauk
Separation of sulfides in a form'of sulfmcides from concentrates
of sulfur compounds and aromatic hydrocarbons in intermediate
petroleum fractions (preliminary methods). Matod.anal.org.soed.
nefti,ikh smes. i proiz. no.1:101-106 160. 4MIRA 14:8)

KMULCIVA Ye.N.; IEYIANOVA., D.Sh.; GALIFERN, G.D.
Synthesis of methyl-l-thiaindanes. Khim.sera-i azotorg.sOed-socl,v Ueft.
i nefteprod. 3:25-33 960. (MIU 14:6)
1, Institut neftekbinicheskogo sinteza AN SSSR.
(Benzothiophen~)

KAP.kUWVA., Ye.N.; GALIWM9 G.D.
Separation of concentrates of sulfur compounds and aromatic hydro-
carbons by seledtive oxidation and chromatographyp following the
e3mmple of the i75-300' fraction of Romashkino oils. nim.sere-L
azotorg,soed.sod.v neft.i nefteprod 3:227-239 J60. (MMA L4.- 6)
1. Institut neftek4ij~icheskogo sinteza AN SSSR.
(Sulfoxide) (Hydrocarbons)

K.araulova, Ye.N,; MEYLLNOVA, D..Sha; GAWFEM, G.D.
Synthesis of 2- and 3-alkyl-l-thiaindans. Zhur.ob.khim. 30 no.10;
3292-3297 0 161. (HM 1~--4)
1, Institut neftekhimicheakogo ainteza AN SSSR.
(Thiaindan)

KARAULCIVA, Ye.N.; GALIPERN, G.D.
Separation of sulfoxides from oxidized sulfur-containing
aromatic concentrates. Neftekhimia 1 no.30315-37-3 lly-Je 161.
(MIRA 16:11)
1. Institut neftekhimicheskogo sinteza AN SSSR.

KARAULOVA,,je.Zj.; SMIRNOV, B.A.; GALIFEM, G.D.
Investigation of sulfides from the kerosene of the Romashkino
oil field. Neftakhimia 1 no,3:339-349 My-Je 161.
(MIRA 16:11)
1. Institut neftekhinicheekogo sinteza AN SSSR.

NUMANOVY 1.11.; Yv~.N.; 13K"INGEH, LN-N.;
Ili - I "'-~ J . ; 'I' i ~; -, ~,'! i i I ~ " I ~ A , T. V.
11 . ' ~ . ; S~* K 0 B 7 , 1' NTA,. ; ; " I
Co'hPosIt! oil, properties, and inethod.,; of e%traction of hetero-
atomic (,omponents from the petroleuins of southei-v Gentral Asia.
Izv. All Turk. S,"R.Ser. fj?,.-U-kh.y khirn. i geol.naulc zio.b':31-35
163. (!,tl I~A 18- 1)
2. Kh j,-niche s 1-J-1 3- inst-Itu'. AINT Tad,,-'ilkskc"y

L 8184-66,-EWT(m).
W
ACC NRI, AP50264621 SOURCE CODE:- UR/0204/65/005/005/074VO7512 t6l
AUTHOR: . Gal I rn, G.1 D~; Karaul Numanovp 1. U;~, Sl~obell
py
_ I,
A* Ik~Chaykos Ve Pe
ORG:. :IngtItjjte-of.~FetroohemI'oal Synthesis iml A, V, Topohlyeva AN SSSR
neftechimicheakogo sinteza AN SSSR)
TITLEO~ Isolation of sulfides.from average petroleum fractions from the,
Rhaudag and Kyzyl-T1~Mhukzfields
-SOURCE:- Neftekhimlyas:v. 5p no.150 1965, 747-7 2
TUIC-TAGS: petroleums petroleum refininsx.\~jpetroleum products organic
sulfur compounds oxidation Ivan-F-e-x-fraction
so
ABSTRACT: The nature of the,organi6 sulfur compounds in the above
central.Asian,petroleums was Investigated. The method used for
.1solating sulfides,-.obtaining concentrates of the sulfur aromatics#.
selectively oxidizing with equivalent amounts of hydrogen peroxides
-c"romatographic separ tio - was also found applicable to high
and h n
sulfur petroleums, 71-Plofthe sulfides present in the 150-35oO
fr~act`onaL of _the two :Petroleums studied were separated as sulfoxides,
L
Elemental analysis indicated that these sulfoxides were mostly mixtures:
of mono- and,bieyclic compounds of various structures,, "Determination
Card 1.12 VDC:, 665,5l(575-4):665,5W-932

DENIS4, S.I.; MENiSjjjK(YVAq G.P.; Q I_ ye-ya-
-,
r"
.Isolation of a dark violet amphorus pigment from the mycelium of
Actin myces fulvoviolacew -strain 9700. Trudy Insto microbiol.
no.8:338 160. (MIU14:1)
1. Institut, eksperixaen'.-allnoy i klinicheskoy onkologii AM SSSR.
(ACTINOMYGETALES)

KARAULOVSKIY, N.N'
Phase phenomena in the formation of conditioned cardiac reflex.
Trudy Vses.ob-va fiziol.biokhim.i farm. 2:43-49 154. OMRL 8:7)
1, Xafedra normalluoy fiziologit Chelyabinskogo meditainskago in-
stituta.
(KLUU, physiology,
conditioned reflex, phase phenomena)
(FCULBX. COIMITIOM'
heart, phase phenomena)

BRUSIIA)VSKAYA, D.; BLMMSTROV, T.; GLASYRINA, L.; KARAULOVSKIY, N.;
KHODOROV, V.
In memory of V.M. Vasilevskii. Trudy Voss. ob-va, fixiol., biokhim.
i farm. 3:1,66..168 '56 (MM 10:4)
(VALkLEVSKII, VIKTOR MIKHAILOVICH, 1907-1954)

SABININA, I.G.; KARAUL'SHGHIKOVA,&Nj FOSLAVSKAYAp O.Yu,; GRANITOV,, I.I.-,
XOGAY, N.A.
I
I,
Leonid Nikolaevich Babusbk-ku; on his 60th birthday. Izv.Uzb.fil.
Geog.ob-va 6tl87-189 162. (KRA 15:8)
(Babushkin, Leonid Nikolaevich, 1902-)

SABININA, I.G.; KARAULISHCHIKOVA, N.N.
- ----- -, -,- -, -- - -, -
Leonid Nikolaevich Babushl7cin; on his 60th birthday. Meteor.
i gidrol. no.7s69 Jl 162. (14IRA 15:6)
(Babushkin, Leonid Nikolaevich, 1902-)

MMNOV, F.A.; KARAULISHCHIKOVA, N.N.
Features of the heat balance of a c1ptton field
of the cotton ball under various conditions of
Trudy Sred.-Az. nauch.-issl. gidrometeor. inst.
Ouring the formation
moisture supply.
no.12sl4-19 162.
(MRA 16:5)
(Crops and climate) (Cotton)

BALASHEVA, Yelena Nikolayevna; ZHITOMIRSKAYA, 011ga Moiseyevna;
KARAULISHG
___HI _)(~!kq,qiko1ayevna; SABININA, Irina
ec~~,
,~evna; SEMENOVA, O.A., red.; VAYTS14AN, A.I., red.;
NIKOLAYEVAP G.S., tekhn. red.
[Climatic description of the Zeravshan Range region] Klima-
ticheskoe opisanie Zeravahanskogo raiona. (By] E.N.Balasheva
i dr. Leningrad, Gidrometeoisdat, 1963. 118 p.
(MIRA 16:8)
(Zeravshan Range region-Climate)

rd:

F,WULOVSKIY2 N. TZ.., Candidate of Med Sci (diss) -- "Aspects of conditioned car-
diac reflexes in aogs under normal conditions and in the experimental patholog-V of
the cerebral cortex". Ufa, 1959. 20 pp (J~ashkir State Med Inst im 15th Anniversary
of VIM), 220 copies (KL, No 21,, 1959, 119)

IKAMUS, Rvzen
Economical use of fuel and power. Energetika Cz 11 no.111555-556
N 161.
(Fuel) (Power resources)

KARAUS, Evzen
How to reconstruct boilers. Energetika Cz 14 no. 4:
173-175 Ap 164.
1. Minstry of Fuels, Prague.

ossi W lity of enstir i ng smol j quant; 4 11 r,,p oi' ni7
steam. nRrr7etiJp, C.,-. 24. no.5: ~3~-22S ',."v '64
4.!,y
k

KARAbS, Evzen
Practical experiences in using Czechoslovak equipment for
liquid fuel utilization in boiler furnaces. Energetika Cz
14 no.10:498-500 0 164.
1. Ministry of Fuels, Prague.

-KARAUSY Evzon
Coal handling equipment of boilers and the effect of stickinesa
of fino grain lignites. Energetika Cz 14 no.12:610-611 N 164.
1. Ministry of Fuel, Pra,gue.

uSSR/Fam Animis. Horses
Abe Jour: Ref Zhur-Biol.., No 4j 1958, 16749.
Author Karelin V.N., Keraush 0. -, Stikan P.A.
Inst
Title The Basic Aopecto of Purebreeding Work with the
Latvian Draft Breed of Horses (Oanovrwye polozbeniya
plememoy reboty s latviyskoy upryaz)3noy porodoy
losbadey)
Orig Pub: Sb. tr. In-ta zootekha. i zoogigiyerq. AN IatvSSR)
1956, 8, 3-35.
Abstract: A breed of draft horses was raised in Latvia and
was approved by the Council of Ministers of the
USSR in 1952. In the production of this breed,
the principal factor was the crossing of Oldenburg
and Hanover breeds of horses. From these crossings
Card 1/2

SOV/107-59-4-7/45
AUTHOR: Karaush, S., Shchelchkov, G., Judges
TITLE: The StronL~,est Took the First Place (Pervenstvo
zavoyevali sillneyshi~~e)
PERIODICAL: Radio, 1959, Nr 4, p 9 (USSR)
ABSTRACT: The authors review the results of the Fourth All-
Union Competition of Female Radio Amateurs and list
the winning radio clubs, teams and individual radio
operators. A total of 685 women particiDated: 324
worked in teams on group radio stations, 29 had their
individual short wave stations, the rest were ob-
servers. Although 74 radio clubs were represented,
the authors complain that many clubs did not parti-
cipate at all and that the number of participants
was considerably lower than during the Third All-
Union Competition. About 50 radio stations operated
by females did not participate.
Card 1/1

:URAUSEMV, A. V.
Some observations on a method of calculating the deformation of
a river bad. Meteor. I gidrol. no.4:98-100 148. (MLEA 8:2)
(Rivers) (Hydraulto engineering)

KAFAUSHEV, A. V.
"Calculation of Drift Distribution in Currents." Trudy GGI, Issue 8 (62), 1948 (40-80)
Meteorologiya i Gidrologiya, No. 3, 1949. 4W Report U-2551, 30 Oct 52.

nova ~n ~,f !-Ilo ~";r

" i.- V."
I. wAtISHEVt
I
2. IJSSR - (600)
4. Dynamics of a Particle
7. Comparison of the gravitation and diffusion t-heoriesof the movement of suspended
particles as applicable to practical problems. Izv.AN SSSR Otd.takh.nauk, no. 12,
1952.
9. Monthl List of Russian Accessions., Library of Congress, April - 1953, Uncl.

KARAU-z-l'--,'-V', A. V.
IIC in n Lon~:itu,-Iri;.l o,' F C-Pmnel Lur-
inc thf, of thH D-vel of Erosion," Tr. Go. ri-drol. ill-t,-. ITO 'n,
a Abst-rict. Ildi, ',!u ~, 1,14-y Y5)
Z~,):!I. liu. '81, "1 Oct

KARAUSUMV,Anatolly Vasillyevich; MAKKAVIYEVA, V.11., professor, doktor
----TAMTN~es ;' t1- , redak-tor; VOLCHOK, K.M. takhnichaskly redak-
tor.
[Hydraulics of rivers and reservoirs (in problem forms Gidrav-
I lilca rek I vodokhranilishch (v zadachakh).Pod red. VA Makka-
veava. Leningrad, Izd-vo "Rechnoi transport," 1955. 290 p.
(Hydratilic engineering) (MLRA 8:8)

KARAUSHEV, A.V.
*-AMMAN
Calculating the distribution of turbidity and deformation of beds on
straight sections and windings of rivers. Trudy GGI no-56:75-95 '56.
(MLRA 10:8)
(Rivers)

,..!WUSHH I ~~ I ; PANCHURIN, Nikolay Alakeandrovich;
!!!~v13gTzIv.;M tQr tekhnicheBkikh nauk, profeBoor, redaktor;
I
LIBEDiV, V'V-, redaktor; VCLOHOK, K.N., tekhnicheakiy redaktor
[Collection of problems in hydraulics] Sbornik zadsch po gidravlike.
Pod obshchei red, V.M.Makkaveava. 14ningrad, Ird-vo 'Rachnoi
transport," Leningr.otd-nie, Pt.2. 1957. 197 P. (MLRA 10:9)
(Hydraulic engineering-Problema. exercises, etc.)

.AP ~?Ous Ili ",
KARAUSHY,V, A.Ve
--~P~Water 'l'eveling on reservoire. Trady GGI no.66:5-16 157. (MIRA 11:1)
(TSimlyansk 3mservoir)
(Isveling)

I , . !, , , 'I
! I "i r.) I/P t ~ I - "-, /, ,
KARAUSHICV, A.Vt
Mr. NOWWWWWAA&Newy~m ',
Investigating and calculating level changes caused by winds i n the
TSimlyanak reservoir. Trudy GGI no.66:17-50 '57. (MIRA 11:1)
(TSimlyansk reservoir)

KARAUS-111--W, A. V. , Doc of T-ech Sci -- (di,.:,,) "Tnc Proble?ns ol' the Dynamics
of I;atuml ',-11'atuer iFlow-s"' -enin,--r-~:d, 3E) Pp -r-,d
0~- - --
~ .'i~-,Lcr L'-amLe;-,,ent) (KL, ii,--)

- KABAUSHNV,-Anatoliy--Vaoil!yevJch;-KAKKAVEYEV, V.M.. otv.red.; IVZ~O,
I.Kh., red.; BRAINIIIA, H.I., tekhn.red.
[Problems in the dynamics of natural water streams] Problemy
dinamiki esteatvannykh vodnykh potokov. Leningrad, Gidrometeor.
izd-vo, 1960. 391 P. (MIPA 13:9)
(Hydraulics)

KARAUWMV, A.Y.; MAKKAVEM. V.X., prof., dok:tor takhn.nauk, otv.red.;
'---rVMMKO, A.Kh., red.; YLAUR, M.Ta., tekha.red.
(Wind waves and swells on reservoirs and lakeal Sgonno-nagonnys
iavleniia na vodokhranilishchnkh i ozerakh. Leningrad, Gidro-
meteor.izd-vo, 1960. 213 p. (MIRA 13:7)
(waves) (Wind pressure) (Reservoirs)

SEI.YUKj Yelena Mikhaylovnal kand. tekhri. nax&;j-ARAUSHEVj A.V., kand.
tekhn. nauk; VEYMT t V.A.., inzh. ; Prinl~ u-cFa--sUy-e--- MSPE
V.Yu.p mladshiy nauchvjy sotr.; GAVRIXDVA, V.P., starshiy tekhmik;
PROSKVHYAKOVO A.,K.t kand. tekhn. nawk, otv. red.; MIRONENKOf Z.I.9
rqd.; SOLOVEYCHTM9 A.A., tekhn. red.
[Investigation, calculationt and prediction of wind waves in
reservoirs; practical manual] Issledovaniiap raschety..i prognozy
vetrovogo vo3jadniia na vodokbranilishchakh; prakticherskoe posobie.
Leningrad, Gidrometeor. izd-vo 1961. 220 p. lioniograms.
(Waves) (ReservoirsT- (MMA 14:9)

KARAUSHU, A.V.; ABAKUMOV, V.I.; NARKUS,, Ye.K.
Method for approximate avloulation of the sedimentation rate of gats.
Trudy Olcean.kom. 8:109-.U3 161. (MIRA 14: 5)
1. Gosudarstvenryy gidrologichoskiy institut Gidrometsluzhby SSSR
(for Karaushev). 2. Proyektnyy institut No.1 Ministerstya stroitell-
stva RO,)'R (f orAbakumov, Markus).
(Sedimentation mid deposition)

KARAUSHEV, A.V.
Ways of studying fluvial sediments. Trudy GGI no.100:3-25 163.
(NiRA 16:9)
(Sedimentation and deposition)

KARAUSHEVJI A.V.
Method of calculating the field of a silt load and the deformation
of reservoir and river beds. Trudy GGI no.10D:88-95 t63.
(MM 16:9)
(Sedimentation and deposition)

RAMMIMINA, N.V.; KARAUSHEV, A.V.
Using a photometer to determine the silt load of water. Trudy
GGI no.100:40-53 163. (MM 16:9)
(Silt) (Photometers)

KARAUSHEV, A.V.
Roiling and spreading of zones of turbidity in reservoirs.
Trudy GGI no.111:81-95 164. (MIRA 17:6)

KARAUSHFV, A.V.; 301,(PIIYFV, N.Ya.; YAKOVIJ',,V, F.I.; ROMANOVSKY, V.V.
Improvement of devices and equipment used in studying sediments
of reservoirs. Trudy GGI no.111:122-130 164. (MIRA 1?:6)

KARA(JS)iF,Vp A,V.
- I- ... .... 1,-.,. -11-- .
Yathod of calculating Bedimentation in reservoirs. Trudy GGI
no.124s26.-39 165. (MIRA l8t9)

"'WIffC-t~~7-AT6025059 SOURC'E CODL: UK/3186/60/000/132/0046/0056
V
K raushev, A. (Doctor of technical sciences; Professor)
ORG: none
TITLE: Turbulence and turbidity in shallow zones of reservoirs and seas
SOURCE: Leningrad. Gosudarstveaayy__&i!Lrplo2i._qhesUy-iaqli-tpt. Trudy, no. 132,
1966. Rezhim, teoriya, metody rascheta i izmereniya nanosov (Regime, theory, methods
of calculating and measuring alluvium), 46-56
TOPIC TAGS: turbidit~tturbulence, ocean current'_r.&hMX1=t1on-
$A
ABSTRACT: This article examines the.jormation of turbulence of water niasses in the
shallow zones of reservoirs and seaO~n the presence of currents and wave action.
Hypotheses are expressed concerning the character of the effect of these factors on
turbulence and appropriate formulas are derived for the coefficient of turbulent ex-
change. The relatively stable values obtained for the experimental parameters of
these formulas indicave the correctness of the dependence of the coefficient of turbu-
lent exchange on waves, current, and bottom roughness which was used. An attempt is
made to perfect the calculation dependences of the turbidity of water masses in the
shallow zones of reservoirs and seas. The theoretical scheme of calculating the
turbidity of water masses examined in this work is more complete titan the previous
scheme which was based primarily on analogies to channel flows. The new.scheme of
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AT6025059
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calculation has still not been checked and therefore cannot compete with the previous
scheme in making practical calculations. Orig. art. has: 44 formulas-and 2 tables.
SUB CODE: 08/ SUBM DATE: none/ ORIG REF: 009
Card 2/2

KARAUSHEVA,.A.I.
Characteristics of the radiation balance of well-delineated area,3
in central Moldavia. Mat.po meteor.i klim. no.liV-101 163.
(KRA 17: 3)

BAZMA,DZIiYAN, R.A.; KARALETYM.I, T.V.; TER-MIKAELYAN, T.H.
Programmed realization of the algorithm of Armen.'azi-Russian
translation. NTI no.12:42-43 163. ! IYTR~~ 17:6)