SCIENTIFIC ABSTRACT SIDORENKO, V.D. - SIDORENKO. V.U.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001550430005-8
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 37
• Document Creation Date: November 2, 2016
• Document Release Date: March 14, 2001
• Sequence Number: 5
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

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'r Y.-.I., V.D.
L 1~1 L Medical LvtittiLe
Title ~1' t,,,u Pieu
Ori - ilub Tr- Kry,.!--k. noti. 1957, 18, 497-502
ll~,Osti-act N:) abstract.
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BUR'YANENKO. A.V, master; SIDQIIEIfKO, V.D., inzhener.
I- ! - --
Simple method for locating cable damage. Elek.sta. 25 no.2:55-56
F 154. (MIRA 7:2)
(F-lectric cables)

KC)MT~~ -AF.OIj -
il -N KC
I .. V. ; L'I-I --LTI, G. L. ; NOViKOV, A. N.; SILOREN , V. A.; SID)RENIKO, V. D.
"Ph:,sical. Studies of Novo-Voronezh Atomic Power Station."
report submitted for 3rd Intl Conf on Peaceful Uses of Atomic Energy, Geneva,
31 Aug-~~ Sep 64.

ooil- fumlirht-.-ir. rast. ot vred. i b-,, no.
(MIRA 17:12)
t,ir3Lly inzir. Yuzhno-U-kra.lnskcy mash InolsDyta tpl n Dy stantsli,
F~ie-son fcr SJriorenko). 2. Srarshiy agronom Yuzhno~Tkrainskoy
T : . -I
ashin:-~IspytatellfiL;y stanteil Kherson (for Vydryakov).
m

S10811611000101410261030
B105/B202
AUTHORS: Kusakov M. M., Konovalova L. A., Prokoflyeva Ye. A...
Sidorenko V. I.
TITLE: Effect of temperature and pressure on the viscosity of
mixtures of mineral oils and organosilicon liquids
PERIODICAL: Referativnyy zhurnal. Khimiya, no. 14, 1961, 543,
abstract 14 M249 (Tr. 3-X. Vses. konferentsii po treniyu
i iznosu v mashinakh. M., AN SSSR, v. 3, 196o, 262 - 270)
TEXT: The authors pre s-ent experimental data on the viscosity of the
I V/
solutions of poysiloxane- liquids (PL) in mineral oils at atmospheric
pressure and in the temperature interval of -50 to +60 0 C as well as at
pressures of up to 3000 kg/cm2 in the temperature interval of from +10 to
+500 C. The viscosity measurements (dynamic) at atmospheric pressure and
at different temperatures were made by means of the capillary viscosimeter
of the type Ubbelohde and at high pressures by means of the falling-sphere
viscosimeter. The components of the mixture were mineral oils MVP and the
spindle oil AU as well as ethyl- and butyl polysiloxane liquids. The
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S/061/61/000/014/026/030
B105/B202
Effect of temperature and pressure ...
authors give temperature curves of the viscosity of the oils MVP, AD
and of three PL. An addition of PL to the oils MVP and AU improves the
temperature curve of their viscosity by increasing its slope in the field
of low temperatures. With simultaneous addition of PL and high-molecular
thickeners -to the oil, the effect of PL mainly causes an increase of the
temperature slope of the viscosity temperature curve; the effect of the
-thickener leads to an increase of the viscosity level. The effect of PL
and the thickemerls-- becomes manifest independently. For all temperatures
investigated the effect of PL is the stronger the higher the pressure.
The results of the study of the piezometric dependence of the viscosity
of the mixture of mineral oil and PL showed that the viscosity of the
mixtures at given pressure is no additive property. The deviation of the
viscosity isobars from the linearity increases with increasing pressure
and with increasing difference in the piezometric coefficients of
viscosity of the oil and PL. With increasing pressure and at a certain
ratio of the components, the Viscosity isobars of the mixtures show a
certain minimum. With addition of various commercial PL to the oils, the
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S/061/61/000/014/026j/030
B105/B202
Effect of temperature and pressure ...
character of the change of the relative viscosity depends on pressure and
temperature. In this case relative viscosity decreases with increasing
PL content in the mixture. With increasing concentration of PL in the
mineral oil the piezocoefficient of viscosity decreases. Abstracter's
E
note: Complete translation J.
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TERM -YEVA ' Ye-.M.; SANIN, P.I.,; STEPANTSEVA.. T.G.; KUSAKOV, M.M.;
SHD4ANKO, ILA,; _~~RENKO, V,I.
Synthesis and investigation of the ultraviolet absorption Bpectra
of hydrocarbons of the 1.1-diphenylethane series. Neftekhimiia
1 no.2:11+1-148 mr-AP 61. (MIRA 15:2)
1. Institut neftekhimicheskogo sinteza AN SSSR.
(Hydrocarbons--Spectra)

TOPOHIYE;V., A.V~; MMi,-LIU7, G.M.; KISLINSKIY, A,Ii-; ILLTOVSKILYA, M.A,-
ANIKINE) G.N.; SIDCREMO, V.I.
Conversions of cyclopentane, dekalin and tetral-in into arormatic
hydrocarbons in the presence of almunosilicates. 1,,'eftekhimiia
1 no.2:204-212 Mr-Ap 161. (MIR!, 15:2)
1. institut neftekhimichoskogo sinteza AN SSSR-
(Hydrocarbons)
(Aluminosilicates)

SHIAWUNKO, N.A. ; POY-PO",,"~;KAYA, Ye.S. ; SIDOPEITKO, K. 1.
Syvt~iesis and ultraviolet absorption spectra of decylxylenes,
decy1mesitylene, and cyclopentyldocyl-p-xylene. Neftekhimia I
no-3.,297-304 My-Je 161. (MIRA 16:11)
1. Institut neftekhimicheskago sinteza AN SSSR.

S/04 62 o26/*010/0061/013
B1 1 7Y111 8/6
AUTHORS: Shimanko, N. A., Shishkina, M. V., Kusakov, M. M., and
Sidorenko, V. I.
TITLE: Absorption spectra of diphenyl alkane series of- flVdro carbons 4-in
the near ultraviolet
PERIODICAL: Akademiya nauk SSSR- 'Izvestiya. Seriya fixicheskayal
v. 26, no. 10, 1962, 1252-1256,
TEXT: Absorption spectra of isooctane solutions of several polycyclic
aromatic and naphthene-aromatic hydrocarbons, C 14 - C329 with isolated
~ an "Uvispek"
benzene rings, were examined at room temperature usinr
spectrophotometer, the compounds being as synthesized by Ye. M. Terentfyeva
et al - Neftekhimiya, 1, no. 2, 141 (1961)), M. G. Rudenko and Al. A.'
Petro,, M. prikl. khimii. 34, 613 (1961)). All the,spectra except that
of 1,1-diphenyl ethane were obtained for the first,time (Figs. 1-4). It is
shown that the spectra of hydrocarbons belonging to the 1,1-diphenyl ethane
series can be well simulated by adding the absorption spectrum of mono-
substituted benzene to that of the corresponding polysubstituted benzene.
/d., 1-?
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S~04Y6 2/02 6/o 10/00 6/1013
Absorption spectra of diphenyl ... B 17 B1-66
The total curves so obtained, representing characteristic spectra of
complex molecules, indicate.the number and position9f each absorption
minimum and maximum. This method is proposed for the structural analysis
of the components of bicyclic hydrocarbons. There are 4 figures.
Figs. 1-4. Absorption spectra in the near ultraviolet.
Legend to Fig. 1: (1) 1,1-diphenyl ethane; (2) 1,2-diphenyl propane;
(a) isopropyl benzene; (3) 1,1-di44-isopropyl-phenyl~-hexane; (d) 1-methyl-
4-isopropyl benzene.
Legend to Fig. 2: (4) 1,2-di-(paraxylyX)-propane; (a) 1,2,4-trimethyl
benzene; (5) 1-phenyl-l-(paratolyl)-etlran~; (6) I-phenyl-l-(paraethyl-
phenyl)-ethane; (0 isopropylbeazene + 1-methyl-4-isopropyl benzene.
Legend to Fig. 3: (7) 1-Dhenyl-l-(2,5-dimethyl-phenyl)-ethane; (8) 1-phenyl~
1-(2p4,5-trimethyl-phenyl)-ethane; (9) 1-phenyl-l-(2,4,6-trimethyl-phenyl)-
ethane; (a) isopropyl benzene + 1,2,4-trimethyl benzene; (10) 1-(paraxylyl)-
2-hexyl-4-phenyl butane.
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TU 49,3ii-65 DIT(m)/WP(j) Pc-4 RM
ACCESSION MR: AR5012257 UR/00581165/000/003/DO34/DQ34
SOURCE: Ref. zh. Fizika, Abs. 3D254
AUTHOR: Kusakov, M. M.; Ki)razov. A. M.; Sidorenko V. I.; Shimanko, A.;
Shishkina, M. V.
TITLE: Some properties of the infrared and ultraviolet absorption spectra of
naphthene-aromatic ketones
CITED SOURCIE: Tr. Komis. po spektroskoDii. AN SSSR vyp. 1, 1664, 370-381
TOPIC TAGS: ir absorption spectra, ultraviolet absorption spectra, naphthene
aromatic ketone
TRANSLATION: It is shown that the frequency 1675 cm'-1 of the v.alent.number for the
carbonyl ketone group keeps its value when the 5-member naphthene cycle is changed
to a 6-member cycle and during the injection of various numbers of alkyls into
naph-tbene and benzene cyclic compounds. The carbonyl group affects the frequenay
of the deficiency number of C-H aromatic nuclei bonds'. In theinfrarea absoxption
spectra a series of characteristic ban.-Is was found, which madt'it poisible to dis-
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CCESSION NR: AR5012257
ttinguish between the spectra of these ketones with 5- and 6-member cycles and to_
~
lidentify naphthene-aromatic ketones derived from naph-thenic acids. Three speci-
!fied absorption regions were found in the ultraviolet absorption spectra: 3000-.
3500, 2400-2800 a Ind 2200-2400 A. The second region characterizes th6 number, pasi-
tion and nature of substituents in the aromatic ketone compounA, and.the third--
an ub
the presence of a carbonyl group, the nature of the aromatic Ucleus: d its s
stituents, and also their 'number and position. This latter region can, be used for
characteristics of the degree of reduction of ketone's to corresipondih' hydrocarbonso
g
SUB CODE: OF ENCL,. -.00
a
J.
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ACC NRz AP6031297 SOURCZ- CODE: LTR/0366/66/002/009/1549;11553
,,,,U-HW,jj 1~,Ijkjtjn, V. I.; Sidorenkop V.
OPG: Chomistry Institute, Academy of Sciences, Tadzhikskaya SSR (Institut khimli
,Q,adumii nauk Tadzhikskoy SSR)
.L.LME: Teetiary trihydric alcohols of the acotylono andethyleno series and their con-
versions. Part 33: Synthesis of acetylenio lj2$5-glycorins containing a phanyl radi-
cal and of their chlorohydrins
SOURCE: Zhurnal organicheskay khimJi, v. 2, no. 9v 1966, 1549-1553
TOPIC TAGS: acotylono compound, chlorohydrinv glycerin
AESTL'~'M: The study was undertaken in order to obtain acetylenic glycerins coetaining
a phenyl radical ar,~ determine whether this has a substantial influence on tho course
of subsoquont 0-.dmical convorsions of such glycorins. The triter-tiaz7 acetylenic
glycorins
CIIIICOII(CI13)COJI(CI13)C=CCO'I(CI]3)2
C1111COH(CIII)COM" )C=CC0"(C1'3)C2"fi
uDcs 547.426-314.2+ .185'131
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ACC NR: AP6031297
oil Oil
C'll'CO 11(c ll')CO ll(Cll3)C=C
OV)
were synthesized by condensing methylphenylacetylcarbinol with the corresponding torti-
ar-j athynylcarbinols. The glycerins are stable compounds; they can be distilled under~
reduced pressure and can be stored without appreciable change. Glycerins I-IV were
then converted into the con-esponding chlorohydrins by the action of phosphorus pont-
oxide, with which they reacted readily. The chloro-hydrins formed wares
cl
CIIIICCI(CIII)CCI(Cil:,)C=CCCI(CI13)2 coli'M(C113
)CCl(Cll3)C=C
M
C1111CO 11 P11) CC'(C 11 3)C=_c CC I (C 113)2 0 X)
(VI) C1
COIIICC1(CIII)CCI(CI13)C=-CCCI(CI13)C2"6
(VII) . I" - C6115CC(CI13)CCI(CI13)C=-C~~
C,115COH(CIII)CCI(CI13)C=-CCCI(C'13)C2'16 M
(Vill) C1
C4l16CO11(C113)CO11(CH3 )C=C\