SCIENTIFIC ABSTRACT SHARGOVSKIY, R.I. - SHARIKADZE, D.V.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001548610018-7
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: August 23, 2000
• Sequence Number: 18
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

UVAROV, V-V., Prof., doktor teldin.nauk; LEBEDYANSKIY, L.S., konstruktor;
OUMOV, V.S., inzh.; CBMN013ROVKIII, A.P., k-and.tekhn.nauk, dots.;
SHARGOVSKIY, R.I., inzh.; SHEFILOV, V.P.. inzh.
The 6.000 hp. gas tiirbine locomotive constructed by the Kolomna
Plant. Izv.vys.nnheb.zav.; mashinostr. no.6:104-108 '58.
(MIR& 12:8)
1. MoLikovolcoys vyBoheye takhnicheakove nchilishche im. Baumana
i Kolomenskiy teplovozostroitellnvy zavod im. Ktkybysheva.
(Gas turbine locomotives)

SHLRGOVSKIY, R.I., inzh.
First Soviet gas-turbine locomotive. Zhel.dor.transp. 42
no.1:21-22,48b-48c Ja 160. (MIRK 13-5)
1. Zamestitell glavnogo konstruktora Kolomenskago toplovozo-
stroitelinogo zavoda.
(Kolomna--Gas turbine locomotives)

SHARI. PERIN, L.L. rodaktor; -BO13ROVA, U.N., tekhni-
chaskly'
[Devices used in repairing electric locomotive equipment] Prispe-
sobleniia dlia romonta oborudovaniia elektrovesev; oprt r&bot.V
kollektivov alektrevoznykh depo alektrifitairovanzykh uchastkov
Sev'prnoi, Sverdlovskoi i IUzhno-Ural'skoi dorog. Moskva, Gee
tranap.zhal-dor.izd-vo. 1957. 66 p. (MIRA 10:63
O'lectric locomotives--Repairing)

77
CoAdensation of o-formylbeaggN ~ASVth', Aa.
U Mink
Zhur., Kkim. 19SS,- No. 2054. -;-A mixt. nf -
anhyd. Na salts'of o-OHCC4H4COX- and (HOsCCH,)i-..
(0.052 mole each) heated M brs. tit 110-25' with 0.103 mole,
Ac~O. the product treated with'1:1 HCI. and the oily sub-
stance sepd. and extd. with ether lidded 28% of o-ctu~
boxyphenylvinytacedc add, m. 66-7 . Frotu the ackfified
aq. layer were sepd. t)..OHCCACOji 40.1 and (HOr
CCII,h 44.10/0 of the original quantities, Heating on-a
boiling water bath 32 hrs. Increased the yield of the conden-
sation product to 37.690. M. Hoseh

A7THORS: 11~ -arov, I N., Sh--rifkanov, A. Sh., 62-58-4-9,132
1
TITLE: Heterocyclic Com--ou-ndz; (Geterotsirklicheskiye soyedinendya)
Communication 58: Anesthetizing Synthetic
(Soobshr-lieniYe 58: Sinteticheskiye obe7bolivayiishchiye
ves',ic'ie.,,~t-.ra).XI"'.S.,-nthe,-~is of Bcn,~,-)ic L-~id Phenylacetic
T,'-1-C---of1-A1kai.1Y1- 2,5-Dimethyl-z~-Ethynyl -,~--Pipcridoles
j T It
(XIX.Sinte:; i fenoksiuksusn,~:'. efirov 1-a1!:en--;1-295-
rERIODIC,!T: Izvestiya Alzaleizii 111-~uk SSSR Otdeleniye Khil.-.,ic',ieski',-..,l Nauk.,
1,058, Nr 4, pp. 446-451 (USSR)
ABSTRACT: As t1he authors coi=unicated alreLdy earlier (references
1-4) they carry out systematic inVeSti--L.tiOnS Of thle
svnthesis of new anesthetic si-,')L;~-ances in t~.eir laboratory.
T'ae pur-ise of this --,.i:.er was to e.-,--,)lcin tile ini'luence of
unsatUrcted ra'icals at tl~e nitro-en on '61,e -
I - physiologic
activity of 'Oenzoic and phenylacet-ic esters of 2,5-dimethyl-
.11 were
The resi~lts of this exuer4
t'-o By cordensation of 1-alkenyl-2, 5-di=ethyl-
Card 1/13 d- i-eri3ole -.,.,ith ~~cetylene at 5 atmos-leres excess pressure

62 - 5.9 -41 -0/3 2
Heterocyclic Con~lounds. Co;.-.~unication 58: Ane-,,tl,,etinin-- Su-
stances. XIX. Synt-,esis of Dcnzcic and Phenylacetic Es.ers of 1-Alkeny.1-1-2,~
5-Dimethyl-4-Ethynyl -4-Pi- Pridoles
Vie corres,,"onding 1-al':enyl-2, 5-di:-ethYl-4-et_qyny1_pi=pe-
ridole was produced in great yields (form""lae I - III)
isomers llicli se;iarat.e
namely as a mi;~titre of otere OCI!e74Cal w,
into individual co!:ipounds by means of partia-1 crystalliza-
tion of the hydroc'ilorides. By the esterification of the
pil)eridoles (formulae I - III) b., means of c~'ilor_'ne anhy-
drides of benEoic and phenylacetic acids their bonz-oic and
phenylacetic esters were proilLced (fDr--_ul_ae IV - VIII).
The lLti-er were subJected to a P,-,rmacoloilical investifation
with reEard to their --nest-etic ef~'ect. It sliowed 'l-t
with rel~ard to this effect benzoic ester of 1-crotyl-2,
5-dimethyl-4-et!iinyl-4-ri.-eridole .,;as the --ost valuable
of t1lese esters. Thiere is 1 table, and 7 refererces, G
of which are Soviet.
Card 2,13

,2-53-4-("/32
6 1
Heterocyclic Com., ounds. Co.,.-nunicaation 5B: Anesthetizin- Synt'.etic Si-,')-
stances. XIX. Synthesis of Bunzoic and Phenylacetic Esters of 1-Alkyl-2,
5-Dirie thyl -4-Et hin.y! -4 - PiIo eri doles
ASSOC !.~ITION: o:,,- -.-nic'.,es):oY Ichinii ir:i.N. D. ZeIirs!:o,-I-o Akadem-ii
n-uk 3';,'3I',KazakhskiY :o2udarstvannyy universitet ir,
S. 1-.!. (Injti.ute for Or n i c C!-i -:' -istry i-eni IT-D.
elinskiy,AS USSR andKazakh State University 5. U.
K-irov)
SIUBIfITTED- November -70, 1956
AVAILABLE: Library of Con--rcas
1. Heterocyclic compounds 2. Denzoic esters-Synthesis
3. Phenylacetic asters-Zynthesin
Card 3/3

62-59-4-10//32
AUTHORS: Nai:arov, 1. N., A. S',,..,. Danilov---, K.F.
TITLE.- Heterocyclic Cor.~ounds (Geterctsiklicheski,~,e soyed-ineniya).
Communic--tion 59: Anesthetisin~; Synt~-etic Su':lsta-ces
(Soobsliclieniye 59: Sinteticheskiye obezbolivayushchiye
ves.qchestva). XX. Syntl-esis of the Benzolc and Phenylacetic
Esiers 1-Alkenyl-",5-Dimeti!Yl-4-Etl'.Yi-4-T-'i:,eri,~loles( xx,
bon.,wyn,,rkh i fcnoksitiksnsnyk-11,,, efirov 1-alkcnil-2,5-
PERIODICAL: I~~ve3tiya Akademii Nauk SSSR,Otdeleniye Xhimicheskikh Nauk,
195,92 1'r 4, 452 - 459 (USSR)
ABST'!XT: In the previous work some bQnzoates anai plicnoxyacet-ates of
I-al.'~
with propylene. Dehydrogenati 8n of this fraction gave 2,6-dimethyl
naphthalene, m. p. 110 - 110.5 C (from CH 30H), which indicates the
presence of 2,6-dimethyl decalin in the alkylate. [Abstracter's notet
Complete translation.
Card 2/2

LIEICHTIYEV P
I S.D.; SIURIFOVA, S.M.; MMMOVA, B.A.
Esterification of terephthalic and isophthalic acids with
various alcohols. Azerb. khim.zhur. no.3:55-59 161. (MIN. 14:1-1)
(Terephthalic acid) (Isophthalic acid) (Esterification)

IEKHTIYI,T,, S~D.-, SHARIFOVA, S.M.; SHIRNOVA, V.P.
Method of separating mixtures of isephthalon-4trile and terephthalonitrile.
Azerb. khim. zhur. no.1:31-34 165. NIRA 18s7)
1. Institut neftekhimicheskikh protsessov 91 AzerSSR.

F, !.! T
SHA'CF0VA, S.M.;
.a
r c P- t i o r, o f t e -, ean d
pr!.,P%,-y alLiphatic alcohols. Azerlb.
A
I. Ingtitut neftekhirnicheskikh protsesso-, AN Azer~S,',.

~M wp(m) /Turt6n) lpwpr i I /q, ww/nA/m
ACC-1Ws-7KP'6M51O5 SOURCE CODE: UR/0316/65/000/005/0006/0009
AUTHOR: Mekhtiyev, S. D.; AMAAMj Smirnova, V. P.; Babayeva, N. L.;
Mamedoya, �h-. F.
ORG: INKhP AN AzerSSR
TITLE: Investigation of/the quantitative isomer composition of mixtures of ge- 4md
isophthalonitriles
SOURCE: Azerbaydzhanskiy khimicheskiy zhurnal, no. 5, 1965, 6-9
TOPIC TAGS: polarography, phthalonitrile, quantitative analysis
ABSTRACT: In connection with the increased production of phthalonitriles, a need
exists for convenient methods of determination of tere- and isophthalonitriles. This
work deals with the quantitative polarographic determination of the above isomers.
In dropping-mercury-ele trode'lexperiments conducted against a 0.05 N LiCl background
the basic reduction cui-v-es--o-f-~he two isomers were shown to be of the following type
(see Fig. 1):
(Fig. 1. Polarogram of terephthalonitrile
(1) and isophthalonitrile (2) against a
background of 0.05 N LiCl. C - 0.26 milli
mole/liter
L-~ar4- I

ACC NR, AP6005105
The pronounced plateaus facilitate determinationo-f the diffusion cu The calibra-
tion curve was based on the first wave of terephtnalonitrile, since its second wave
tends to overlap with the first wave'of isophthalonitrile. Quantitative determina-
tions by this method differ by only 2-4% from those obtained by melting point deter-
minations. The two methods are thus mutually verifying. Orig. art. has: 4 figures
and I table. [VS]
SUB.CODE: 07 SUBM DATE: 29jun65/ ORIG REF: 007/ ATD PRESS:41?ql'

~6XiaOV, h.F.; OBOROTOV, I.Ye.; KALYADIN, I.I.; YELBIZO, L.I.; FXREPFLITSA,
V.R.; NECHtiYEV, B.11.; DiLTYXV, -h-M.; MMV, N.G.; CHUVAKOV, F.F.;
FILIKOV, P.V.; LtRIKIN, G.D.; SVYrTKIN, V.V.; SP.,RIYUL.LINM,.
Railroad workers address metallurgists. Put' i put.khoz. 4
no.8:14 Ag 160. (MIEL& 13:8)
1. Kovylkinskaya distantsiya puti i putevaya mashinnava stantsiva
No.66, stantsiya Kovylkino, Kuybyshevskoy dorogi. 2. Nachallnik
Kovylkinskoy distantaii puti (for Maka-rov). 3. Sekretari
partbyuro, stantsiya Kovylkino, Kuvbyshevskoy dorogi (for Oborotov,
Nechayev). 4. -Predsedatell mestkoma, stantsiya Kovylkino,
Kuybyshevskoy dorogi (for Kalyadin). 5. Sakretari Vaesoyuznogo
Leninskogo kommunisticheskogo soyuza molodezhi, stantsiva
Kovy-lkino, Kuybyshevskoy dorogi (for Felenko, Ivanov). 6. Nachall-
nik putevoy mashinnoy stantsii Mo.66, stantsiya Kovylkino,
kuybyshevskoy dorogi (for Perepelitsa). 7. Chlen meatkoma, stantsiya
Kovylkino, KiWbyshevskoy dorogy (for Aavydov). 8. Rukovoditeli
brigad i udarniki kommunisticheskogo truds. distantsii i putevoy
masbinnoy stanteii No.66, StaUtBiy Kovylkino, Kuybyshevskoy dorogi
(for Chuvakov, FilIkov, LarIkin, Svyatkin, Sbarifullin).
(Railroads--Rails)

rl Gra'!
U2S
Abs J.~.ar
Gn ".a rL f 'Lil
ins t
V'. t',,~ V,:Ir
T! 1AL:
Oric ?U') j)al
1)57~ 1.::~ 4, 3-7.
Cara 1/1

sc,V/92-58-7--20/37
Oil Well Gas Should be Used (Cont.)
It is 21earl therefore, that cAl Twrell flow cam b~a vith the of
oil vell gas.
ASSOCIATION: Promyzal No. 2 ITPU B&~r'lyneft I (011fi-alal No. 2 of the Ba7riymeft I
Adrn!.nistrvUcn),
1. Petrolewm-Production 2. industrial prod uc L ion-,,1easurament
3. Control systems-Pe:i.,formance
Card 2/2

104) SOV/20-127-6-ii/51
AUTHOR: Sharikadze, D. V.
TITLE: The Application of SimilaritytD the Motion, and the Point
Explosion in the Magnetic Dynamics at Infinite Conductivity
of the Gas
PERIODICAL: Doklady Akademii nauk SSSR, 1959, Vol 127, Nr 6, pp iia3-iia6
(USSR)
ABSTRACT: The present investigation is carried out under the condition
that the tension of the magnetic field can be represented
as an exponential function of the entropy. For this easel
equations (1), (2), (3), and (4) are indicated for the non-
stationary flow of a gas. Equation (5) indicates the current
density neglecting the displacement current. From equations
M-W, the equation system (9) is obtained by eliminating
the pressure and the quantity h. The solution of this system
is indicated by equations (10), and the integration of the
initial equation system W-W for the application of similari-
ty to the motion is reduced to the quadrature of two com-
mon differential equations of first order. The case of a one-
dimensional flow is then investigated, and subaequently the
point explosion in the magnetic gas dynamics is considered.
Card 1/2 Equations (22) give the conditions in front of the shock vave,

SOV/2o-127-6-11/51
The Application of Similarity to the Motion, and the Point Explosion in
the Magnetic Dynamics at Infinite Conductivity of the Gas
and equation (23) indicates the total energy of the shock
wave at any point of time. The integral (24) is obtained for
the total energy from (22) and (23). From the results thus
obtained, the distribution of the parameters in front of the
shock wave is investigated, and it is ascertained that it is
different from the case of point explosion without a magnetic
field. The author thanks Professor K. P. Stanyukovich for his
interest in the work, and Acalemician Ya. B. Zelldovich for
his valuable advice. There are 4 Soviet references.
ASSOCIATION: Moskovskiy gosudarstvennyy universitet im. M. V. Lomonosova
(Moscow State University imeni M. V. Lomonosov)
PRESENTED: May 9, 1959, by Ya. B. Zelldovich, Academician
SUBMITTED: may 9, 1959
Card 2/2