SCIENTIFIC ABSTRACT STERLIGOV, D.A. - STERLIN, B.P.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001653310005-7
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 3, 2016
• Document Release Date: August 26, 2000
• Sequence Number: 5
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

KUROCHKIN, S.S.; DFLOV, A.F.; BEUU3, A..L.; SALIC'ItKO, V.N.; AWZINA, I.:i.,;
K11"tiMilly Ye.V.; Y.UZ'.-`FTSOV, K,F.; STERLIGOV, D.A.
Prinolple trans is torized c(mDonents of multimhannal mms-,Lring
syntems. Mnocrokan. izm. nist. v iad. fiz. no-5:87-116 16 1
(MIR@'@ 16:12)
-9 @j,

S/0058/64/000/002/AO19/AO19
ACCESSION NR: AR4032161
SOURCE: Ref. zh. Fiz., Abs. 2A192
AUTHORS: Krashenninikov, 1. S.; Xurochkin, S. S.1 shalginf Yu..M.i
Sterligov, D. A.
TITLE: System for centralized control of statistical parameters
CITED SOURCE: Tr. 5-y Nauchno-tekhn. konferentsii po yadern. radio-!
elektronike. T. 2. Ch. 2. M., Gosatomizdat, 1963f 123-134
TOPIC TAGS: statistical parameter, centralized control, multiple
pickup monitor, pickup intensity deviation identification,.magnetic
drum memory, two level recording, multichannel control,,-dosimetric
control
TRANSLATION: The operation of a system for centralized control of a'
large number of objects of the same type is analyzed. The control
:Card 1/2.,

ACCESSION NR: AR40321:61
parameter is the intensity of pulsis from pickups, which number 600-
in this case. The system registeri deviations of the monitored in-
tensities from normol and records the number of the pickup in which
this deviation takes place. The period of scanning the monitored
objects is 30 minutes.; The system'is suitable for an average pick-
UP pulse intensity -109 pulses/sec! The number of pickups which
are read-simultaneously is 256. A@cess to any one group of pickups
is by applying the supply voltage to their electrodes. The main
block of the control system is a magnetic drum memory unit capable
o--* storing 50,000 bits of information. The drum has 80 tracks and
recording is at two levels with a 30 kcs timing frequency. The
block diagrams of theinain units are given. The use of the system
for multichannel control (for example, dosimetric control) can in-
i crease the control accuracy and decirekse the quantity.of electronic
equipment per control point. Yu. Semenov.
DATE ACQ.- 3lMar6"4 SUB COPE:. SD, PH ENCLt 00
Card 2/2.

ACC NR, AR6016152 SOURCE CODE: Woo58/65/000/01VA026/AO26
AUILNOR: Belov, A. F.; Kurochkin, S. S.; Stergiloy, Do As
TITLE: Matrix-type control devices for multichannel analyzers
_ .
SOURCE: Ref. zh. Fizika, Abu. IL4273
REF SOURCE: Tr. Soyuzn. n.-i. in-ta priborostr.p vyp. 1, 1964, 131-142
TOPIC DIGS: pulse analyzer, measuring apparatus, control circuit, computer logic,
computer program/ Buu-16 pulse analyzer, - E@ L-17 pulse analyzer
3' li
ABS-,J1ACT: r1lie authors analyze variants of control circuits for multiplecbannel mea@
suring systems: linear, decoding, and matrix types. It is concluded that in the pre-
sently developed analyzers it is a4vantageous to use a control device of the Matrix
type (when the number of command steps exceeds 16). Two types of control devices, 1@
BUTU-16 and DUU-17, are described in detail) and their schematic di-CCrams are presen ed
together with their basic data. The operation of the individual units is considered,
such as the shaping amplifier with an OR logical circuit or without it, the address-
current generator, and the program transfer switch. Results of tests and operation ol
the control devices of the matrix type are presented. It is noted that the type of
control device under consideration was realized in the following analyzers: Al-1024-3
AI-1024-2, Ai-208, etce X. P. (Translation of abstract]
SUB CODE: 09

').A.
A OF. - STIEFU ` (;'-@Vy ;
Adjustment. no-.trol of of trultTiharnel
-1
mea5lir Lng ays tem.3. Nau-.h.-I.Ab. sh@- . lloz3. I d ,r-i i It. v obl.
titom. nwaki i tekb. no,6:105-113 1&3 170)

L 36716-M EWr(d)/EWT(1)/EWP(l) IJP(c) BC
ACC NR: AR6014198 SOURCE
AUTHORs Belov, A. F.1 Kurochkin, S. S.1 Sterligov, D. A.
TITLEt Matrix control devices for multichannel analyzera_
SOURCE: Ref. zh. Avtomatika, telemekhanika i vychisliteltnaya tekhnika, AbB. 1IB228
REF SOURCE: Tr. Soyuzn. n.-i. in-ta priborostr., vyp. 1, 1964, 131-142
TOPIC TAGS: multichannel analyzer, matrix control, digital computer, computer
component
ABSTRACT: Linear, decoder, and matrix control devices for multichannel measuring
systems are analyzed. It is inferred that the matrix type (when the number of
command cycles exceeds 16),kis expedient for use in new analyzers. TwoAcontrol.
devices, BUU-16U6and PP-Inare detailed, their functional diagrams are presented
as well as o basic data. Operation of these units is examined: a shaping
amplifier with or without an OR-gate; address-current generator with a program
switch. Tests and operating-experience resultsjLre reporte(;@ The abovefontrol
device was physically implemented in AI-jO24-V('Aj=jO2 and I lyzers,
A8 ana
AAII-:20
Nine figuros. Bibliography of 4 titles. N. P. [Translation of abstract] it
SUB CODE: 09
Card 1/1 j@VJ

KU211411LA, N.G.; FEOKTISTOV, Y.N.; M&TVETNV, V.V.; STERLIGOV, I.H.;
RYVEIN, S.B. - - -
New develo-monts in testing oil cloth and bookbinding
materials. Kozh.-obuv.prom. no.12:19-23 D '59-
(MIRA 13:5)
,(Leather substitutes-Testing)

IAJZHNYKHg L.A.; SITIILIGOVp 1.14 YEVSYUKOVO P., red.; PORTYANSMt B.,
p
zCI-Iv9r'--v
red. i ANSIMAg 7a, tekbn, red,
(Automation; collection of
tekstov na agliiskom iazyke.
L.A.Luzbmykh i I.N.Sterligova.
iazykakhq 1961, 129 p jAutomation)
articles in
Podbor tekstov,
Moskvat
English]
Avtomatika,- sbornik
kommentarli i slovarl
Izd-vo lit-ry na inostr.
(MIRA 14:7)

ACC NRt Ap6o19946
CODES IM/0323/66A)OO/001/00 /0057
Sciences);!
AUTHORS Protasov, V. G. (Engr.); Baramt2M@j N- K. (Prof.; Dr. of Chemical
Baranova.- L, P. Engr.); Sterl1gov, I. N. @Engr.)
ORGI Physical and Colloidal Chemistry Dapartment, Moscow Technological Institute i
of tho Ught Industry (Kafedra fizicheskoy i kolloidnoy khim@i Moskovskogo tekhno-
logicheskogo inatitut legkoy promyshlennosti)
TITIE1 Study of adhe:ive "based on modified polyethylene I-J,
SOURCES IVUZ. Takhnologiya legkoy prozUshlennosti# no. 19 1966, 54-57
TOPIC TAGS1 adhesive, polyethylene plastic, footgear, polypropylene plastics =919ic
anhydride
ABSTRACTI The possibility of using modified polyethylene as an adhesive for bonding
footwear and sawing materials was investigated. The mechanochemical modification
of polyethylene involved the use of a laboratory extruder; malsio anhydride (M) was
introduced to. increase the polarity, " atactic polypropylene (APP) - wu added as a
plasticizer.N'2 7he properties of the adhesives were tested by bonding footwear and
sowing materials in various combinations. Adhesive bonds in footwear materials were
tested for ply separation, aM in sawing materials, for ply separation and shear.
It was found that as the atactio polypropylene content of polyethylene risest tho

L ";--3641-66
ACC NR, AP6019946
resistance to ply separation Increases; this is attributed to the plasticizing
effect of APP. The addition of MA to the adhesive composition increases the adhe-
sive strength by increasing the polarity of polyethylene and atactic polypropylene
(by forming carboxyl groups). It is concluded that the use of modified polyethylene
offers attractive new prospects for the production of inexpensive and efficient adhe-
sives for the footwear and clothing industry. Orig. art. hass 2 figures and 2
tablou.
SUB CODES it/ SUBM DAM 20Aug65/ ORIG REFS 004/
.-I-

STERLIGOVY 0. D.
"The effect of the diameter of Laboratory columns with fenske pacing on their
efficiency and productivity"., Kasanslq,, D. A,, Liberman, A. L. and Sterligor, 0. D.
(P. 130)
SO: Journal of General Cher"t (Zhurnal Obshchei Khimii) 190, Volume 13, no. 3.

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vlolvblenum Cgtalysts.ll Slib Apr -1, Inst
Acal scl USSR.
Dissertations preseqted for acje.,-.::e and endinnerln6 defroea
4n Anccow lurliiE 1951.
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Ng 'J. fna". Affigm.
N4Uk IOS3. 103.542.-ExehAnge of H atoms was studied in
x-Glho. x-Cirlin, NeCHEts. PrOlAfeEt. BuCMe,. Mer-
CHM4, and Me,CIlCHtCNIc, in contact with D-enfiched
HISQ,. H--D excbRngc takes place only wl III tho" hy.
idromborts that contain a tertin, C atom and the exchange
ele"ll*isatL.Jnedat2O-5*witllill.,yfewlirs. 11FROInsinsatd.
0 Ycllc comptis. which contain a tcrthw-C FAtorn arc also
readliv txchAwted for. D. G. M. Rosolapoff %, ((,@

11?6@vt of to-reo of compregsion oR AONity and ztr@
0 U
-
mQIYtdqntl!n cataIP4-@' 0 -1). Rerliguya A. M
16. 1, In
Cl ema, 953, No. 1. 28 -thj-
-
111@ J-Ri7cTWI o
ctojnprcri@ion on structure. catalytic Oficivacy.
t
, tivitv, antf ttmalitv of catalpt ii investigateil. 1"1111 C'%TwTi-
qw.
Britiah Abet. ';
nic .,I t-unli arc, ip-wtni. catalyst contoining -20% hloO3,
t
, "AtI @ @ A into giantile--i (1-5-A-0 min.) at piessores fr ... n 21HK)-.-
?o cO:: i:to. 13 tv, I in the dvhydrocyclisation of n-ClIll, and
Aug. 1953 %!. !; . !@, -,.@ t,i , -,I, ;-- Mane at 4W1. Activity (if catalN%t Is,
uilibria and Kine tics
Ghomical E ""' @'- 2!) )-'r- if wovi!u"lion of stalling h0rocarfmcm into,
q .11`-M."" . III It- - '-f i,w-ute from 2(0) -ZO.WU atm. ri.,nit-i
"i 4 virwi"FICY .11111 Mabilitv, and a (lawra%c
'Itt, t'l it of poronity in t1w Ca". (It
t 1.11 1, pbjt of 1, V
:@@ ill. tctiittv, s, again4t lime, r. givo;
j
-,i xt. Wit-TO S. Kp. activity At
f;jjI ()f -,p I(.tjVjjy ;Iflkl I/M- 0 ij IIK:((.
tigit'-n sijoxv,il no clianre in primary
%V. MAN/

.3-rERLid-Ov
I rid.
ow MMUSM AMMM of nmwn ad
111181tRAW OMRPOUWIL
RosengUt, - 0. D V an ve
Anal. GkW 1013.
K.Veral dispersion dieth, of detiorraining aromatic
hydrocarbons In mixtures with other hyarocarbons
an discuosed. and a method not requiring determina-
tions of sp. gr. or correction for non-additivity is
rocommenJed. The calculation with binary
mixtures is made by means of the formula-
[(Igor - I Moc - !)/Ixz,- 1) X 10,
W'_,+ 2 - _+2 1
where wx is the relative dispersiom, and "Y' sc and
"I, are the refractive 101cas for the H lines Y and
and the Na line D. G. S. SMITH-

A. L. Mier-
fly-PTOducts In tho. Sandmeyer reallf
H. A. KazarLIJOI 0I
T r -q Prod cl
Y-LaRihimond
Y -Dak-@
q. ca'] U.S.S.R.. gbeicaw, yielding, afte, .2.471ft I= 49% #-U
91 . 845--8(In3)---WhItC.It Is: Recovery at the ors, mitt the ymishinan QNq Ki
tjAilY :11,1UMMI that th the' Sandmeyer - riection the litt" c-MeColli'011, by sityeral derN."
tiocti the pmitj@3!1 previouily occupied by the midue after Its dista.'Pollelffict! and vm@% purVeJ by
grotip, this is n,,t necvssarily@the case. Wheri from H.O. )-lelding: L@q. 64.7-5.3s; berizoate, to.
I M11 0.4', ' to it 4upint. expt., IOAA g. l*-NteC4l1.NH, la 470 tril.
la C O-MCC4114\1 was converted to the Br
I
t';, !@,iudmeycr reaction, and the by-product 'a.*40,. the d -
47% IIPr Wai'djazuti" with 77.0 &Ary N . t.
W- '.Ut4tilly cxanid.. It was found that the@yaatcrLil awnium &aft decom . by 29 Cu,Bn ohd I cu. t
1 finm the main Prtyluct by meam offfltliOii and NnOH the inixt, dlod. witnte, m, Aiklini. 78.6's,' o-
"MeC411,011 but an Oquitnolar thixt.
froin the rore-run of the dista.; the i9k. washes Pvt
[],(fro i C.HsHe (1) (each In,13% yield), ci-cmm)l and 24.7-g. brommesol. Identiml with I '17, 1 1
"In 11-of -C I - .11 %val t reat ed w I t h cofict 1. 11 B r a nd Nit NOj ni.'64.24.40, To 1081 g. a-cresol In 470 mi.,'41 ED';
LIi,i x, o,c.l iii a Samlinever reuction the above. chilled to 0' was added 9 lowly 77.6 g. NAINCh with aking:
ii)t.in,A in 7170 yild. thus affo-ding a then 29 C. CusBri and I g. Cu ikhavjngs; the mixt.mumed to
m:th,x1 for phenols. Ilie Cn3W3 was n0t, 40 V, the pro,luct steartf-distri., the distillate; extd. IF(tk-
t! !: r,.ictirm and the same product (ormcd la'. gtO,andtheettidistd.,givig5g?,L WWenCq.I3rr-C%i"-r
v, higher vidd. Thm NaNO. cun be* omitted, the yickl rd@e to 74 . . o 02 g. Mellh In 470 ml.L
IIIJr -!!i. mni broinina-: - Y. I
toxiditing agent fn@ ~47%ltllrwas-Ll(,%,,IybldetloviWlh atO9T7,dz;WaNQ4'.
ti@- I' L.Cflt N. through the jiu; nAt. wanned I ItE In 3"20, cdoled, Out the Wofm-r@,'
-n,tamt f.p. curve of the pt,xluc, i1r -r di't"'. gave 13% BrCjj4.%fc 110t. Ide'l,
A, 4 ILI% t
.1 @: ! ; 0 @'. 'I he fmc wnine, fr&NI by b)'d-,OIY4L4 with nV
" 1 " g. vortiol-
t!jr,.1 'ti. ti--rJ in 162 in.
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of dstauWa lumwb
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0. V. b v an surumo 4W. CAM,
reply to the
objectufma of I a Abs 2125) tothe
by Kazwsky@ d 41. Ad. bsio.. IOU, i.,
G. S. Surm

-- ----- ----- --- -
STERtICOVP
di=on and comom-tTva
Odis;=',Ot,-i.' me for determi6tion of
hX
a onc H. A KazaA5k P,
algo . a"(1 u. A.
C.A. 48.
L. 11-.

USSR/ Chemistry - Analytical chemistry
Card Vj Pub. 22 -32/63
Authors i Setkira, V. N.; Platep A. F.; ter1ig2_V,_@L-,D_,* and Kursanov,# Do No. Membe.-
Corres. of Acad. of So. USSR 4m
Title i Possibility of adaptirg the hydrogen exchange reaction for the analysis of
saturated by-Imearbon mixtures
Periodical I Dok. AN S3SR, 99/6p 1007-1010, Dee 21, 1954
Abstract I The characteristics of hydrogen exchange reaction and the possibility of
applying this reaction for analytical -purposes were investigated* A com-
pulsory condition for the adaption of the hydrogen exchange reaction for* the
analysis of saturated hydrocarbon mixtures was fourd to be the attainment of
reaction equilibrium. It was established that the hydrogen exchange reaction
of aliphatic and alicyclie hydmearbon mixtures containing from 5 to 7 carbon
atoms in the molecale begins within a period of 10 - 20 hra. The resultso
obtained &xring the reaction of two--component saturated hydrocarbon mixturesp
are tabu2ated. Nire USSR references (1935-1954). Tables.
Institutioni oe#oesosoomes
Submit ted: Jum 18.. 19 54

It-MOVIITKOV, V', V, PLATE, A.F., doktor khtmicbeakil-b nauk, redalctor;
13YXOV, G.V., @-i-ndidat kbinicheskikh nauk, reduktor; PFTHDVSKIY,
I.R., akademik,redai-tor: BTKOV, r.M., akadenik, redel-tor; KAZAN-
SKIY, B.A., ak.@demik,rndaktor; SWMIDT, O.Yu., Rkade'lik, redaktor;
ANDIMMW, U.N. akauemik, redaktor; SHChMAKOV, D.I., akademik,,
rndaktor; TUDIN, P.F., akademik,rodaktor; DW113, B.N., redaktor
Kns!jToyANTs, Kh, S., redaktor-, SA-KhRIN, A.M.. redaktor. LEBEDEV,
D..M.. profesenr, rndaktor: 27GUROVSKIv.. N.A., professor, redaktor;
KTJZITMSOV, I.V., kandidat filologicheakikh nauk, redaktor; STERLI-
GOV, O.D, ro3daktor; ZTTfLYj'LKOVA, T.A., tekhnicheekiy redak1:00'r-I
[Selected wnrks] Izbrannyfg trudy. Redakt9iia, stat'l i primechaniia
A.F. Plate i G.V. Bykova, Moskva, Izd-vo A-kademii nauk SSSR 1955.
Q26 p. (MLRA 8:10)
1. Chlon-korrospnndent AN SSSR (for Delone, Koshtoyants, Samarin)
(Chemistry) (Markovnikov, Vludimir Vasillevich 183?-1904)

3TC-- R L I @-C, V
AUTHORS: Kazanskiy, B. A., Sterligov, 0. D., 62-11-20/29
Belen' kaya, A. P. X`on-d-r-XVyeYs;-, G. Ya.t
Pavlova, P. S.
TITLE: Determination of the Uneaturation of Isopentane-Isoprene-
Isoamylene Mixtures According to Bromometric Methods.
(Opredeleniye nepredellnosti izopentan-izopren-
izoamilenovykh smesey bromometricheakimi metodami),
PERIODICALs Izvestiya AN SSSR, Otdelenie Khimicheakikh Sauk, 1957,
Nr 11. pp. 1399-1400 (USSR)
ABSTRACTs Here a relative evaluation of the exactness of the methods
of bromometrioal determination of the unsaturation and the
selection of the most useful method for the analysis of the
isopentane-dehydration catelyeates is brought. Issmining
the bromometric methods of K. W. Romenmund (reference 1),
G. D. Gallpern (reference 2) and Virabyants with artificial
mixtures showed that in dependence of the composition of the
isopentane-isoprene-isoam.ylens mixtures the exactness of the
determination of the total unsaturation according to the
methods of Rosenmund and Gallpern can vary absolutely from
Card 1/2 1 to 3 @. When introducing correoting coefficients the

Determination of the Unsaturation of Isopentane-Isoprene- 62-11-20/29
Isoamylene Mixtures According to Bromometric Methods.
exactness of the determination can be raised to t 1
Virabyants' method is useless for these mixtures. It is
shown that under the conditions for the brominationj whioh
were investigated, the 2-methylbutene-I binds more than
one bromine molecule. There are 4 tables, and 3 references,
I of which , is Slavic.
ASSOCIATION: Institute for Organic Chemistry imeni H. D.Zalinskly- of
the AN USSR (Institut organicheakoy khimii im. N. D.
Zelinekogo Akademii nauk SSSR).
SUBMITTED: July 5, 1957.
AVAILABLEs Library of Congress
Card 2/2

:7-K- 1 4 160\4
AUTHORS: Kazanwkiy, B. A., Member of the AN USSR, 20-4-20/52
Marushkin, M. N. (Deceased), St--rli,-,ov, 0. D., and
Belen'kaya, A. P.
TITLE: The Catalytic Dehydrogenation of Imopentane
(Kataliticheakaya degidrogenizataiya izopentana)
PERIODICAL: Doklady AN SSSR, 1957, Vol. 117, Nr 4, il,p. 619-622 (USSR)
ABSTRACT: From the economical point of view the use of isopentane is
important for the incruased supplj of raw materials to the
production of ajnthetic caoutchouc. The catalytic dehydration
of isopentane to iso-amylenes and of these to isopren
(C5H12 n* C5 H10 -# C5 H.) can be one of the ways of producing
isopren. There is only little literature on this subject (refer-
ences 1 - 3). So the investigation of this reaction is still
very young. The second author produced at the institute (see
"Association") an active alumochrome catalyzer for the de-
hydration of n-butane and propane which can be employed for
the purpose discussed here. It consists of (in molar-@6/'.)t
A1203 68, Cr203 9, K20 3. The method of tile dehydrogenation
of isopentane is described. In the condensate (by means of
Card 1/3 dry ice) the total unoaturatednezu was determined

The Catalytic Dehydrogenation of Isopentane. 20-4-20/52
bromometrically according to Rosenmund (reference). The
proportion of isopren as to weight was determined by reaction
with maleic aldehyde. The activity of the catalyzer is increas-
ed when the temperature rises. It reaches its highest stage
0
at 550 , The productivity is rapidly increased when the rea-
ction temperature and the supply of raw materials are increas-
ed. At r750 the productivity of the catalyzer decreases
(figure 3) as well as its selectivity as a result of the in-
crea2ing cracking reaction (figure 1). At the optimal temp-
o 0
erature of 550 stability, degree of contamination, and the
most profitable duration of the working cycle were stated.
The average activity (productivity) per cycle decreases with
the extension of the cycle. Figure 4 shows that the select-
ivity ia independent of the degree of contamination. When the
working period lasts for more than 8 hours without inter-
ruption the degree of dehydration falls to almost 1/3 daring
the first 4 hours and then remains so without noticeable
changes. After the regeneration the catalyzer completely re-
reaches its initial activity. The contamination is obviously
connected with the dicturbance of the catalyzer by depo2its
of "coke". When the temperature rises from 5000 to 5500 the
pro,ortion of total [e-mail] almost trbles. The concen-
Card 2/3 tration of isopren increawes tenfold, the concentration of

The Catalytic Dehydrogenation of 1gopentane. 20-" -20/-;2
2-methylbutene-2 almost doubles, of 2-methylbutene-1 treb-1-1,!
whilat the proportion of 3-methylbutene-l hardly changes.
Within the range of these temperatures 2-methylbutene-2 and 2-
methylbutene-1 prevail whil2t the other two substances are
contained in small quantities only. Table 2 shows that one has
to be careful in employing the spectrama of the dispersion of
light combination@ to the analysis of the substances discussed
here, as the lines of isopren and 3-methylbutene-l overlap.
With small proportions of isopren already line 1640 cm-
(of 3-methylbutene-1) but also line 1651 cm-1 (of 2-methyl-
butene-1) which leads to sharply inoreased results for the
last two. There are 4 figures, 2 tables, and 4 references,
3 of which are Slavic.
ASSOCIATIONs Institute for Organic Chemistry imeni N. D. Zelinskiy of the
AN USSR (Inatitut organicheakoy khimii im. N. D. Zelinskogo
Akademii nauk SSSR)
SUBMITTED: July 22, 1957
AVAILABLEt Library of Congress
Card 3/3

'AUTHORS i Kazanskiy, B. A., Oterligov. 7 5 -11 -.2 3/2 6
Be@enlkaya, A. P., Kondra'tlyeva, G. Ya., Favlova, F. Z).
TITLE: Bronometric Methods of Determining Unsaturated Hydro-
carbuns in Isopentane-Isoprene.-Isoamylene Mixtures
(Opredeleniye nepredeltriosti izopentan - izzopren -
izoamilenovykh smesey bromometricheskimi metodami)
PERIODICAL: Zhurnal Analiticheskoy Khimii, 1958- Vol 13, Nr 1, pp 134-141,
(IT SqR )
ABSTRACTi In the catalytic dehydrogenation of isopentare a mixture of
5 components forms - the initial product, 3 isopentenes and
isoprene. The quantitative relation of the components depends
on the reaction conditions. In the present paper the relia-
bility of the three bromimetric methods - according to
Rosenmund (Reference 3)p Gallpern (Reference 5) and Vyrabiants
(Reference 6) is examined. This control was investigated in
pure C -hydrocarbons and also in various artificial mixtures
of is4entane with isopentenes and isoprene shich differed in
the number of components and also in their concentration. It
Card 1/5 became evident that the method according to Vyrabiants is not

75-1-23/26
BromOmetric Methods of Determining Unsaturated Hydrocarlt-ons in Isopentane-
Isoprene-Isoamylene Mixtures
suitable for an analysis of such mixtures, because the error
assumes different values and attains up to 7 - 8 VII. (absolute).
The results obtained according to Rosenmund and Gailparn conv
firm the fact that the accuracy of the determination of double
bonds depends on the structure of the hydrocarbons and on the
composition of the mixture: 2-methyl-butene(2) and 3-methyl-
butene(l) without difficulty absorb 1 bromine molecule on
bromination. 2-methyl-butene(l) and isoprene consume mcre
than 1 bromine molecule and therefore yield too high results,
relative to a double bond, in the determination according to
Rosenmund and Gallpern. The analysis of mixtures with 3 or 4
components, but without isoprene, showed an average absolute
error of the determination of the olefines of + 1 %. On addi-
tion of isoDrene to the mixtures with 3 components the ab-
solute error increases to + 3 %. The analysis of mixtures with
5 components showed that th@ absolute error in the case of an
isoprene content up to 20 % in the method according to Rosen-
mund on the average amounts to + 3 % and according to the
Card 2/5 method by Gallpern -2 10. As the average error in the

75-1-23/26
Bromometric Methods of Determining Unsaturated Hydrocarbons in Iso-
pentane-Isoprene-Isoam.ylene Mixtures
determination of the total number of double bonds in
mixtures of 5 components according to both methods has a
systematic nature, it can be taken into account by the intro-
duction of a corresponding coefficient (in the case of an
isoprene content up to 20 1&1'). It was shown that the values
for the total number of double bonds which were once de-
termined according to Rosenmund and once according to
GalApern practically coincide after the introduction of a
correction coefficient. As the method of bromination only
makes possible a sum determination for alkenes and dienes,
the content of monoolefines can only be determined from the
difference betweer the total number of double bonds and the
content of dienes. In the present case an appropriate cor-
rection which takes into account the content of isoprene must
therefore be applied to the bromimetric results for determin-
ing the content of isopentenes. For the determination of iso-
prene the photometric method according to Robey and Wiese
(Reference 17) was employed which is well applicable in the
Card 3/5 presence of monoolefines, but also of some dienes. The average

75-1-23/26
Bromometric Method of Determining Unsaturated Hydrocarbons in
Isopentane-Isoprene-Isoamylone Mixtures
Card 4/5
error of this determination is less than I ;@ (absolute).
Determination takes 1 1/2 hours, which time can be shortened
in series determinations to 20 minutes for one determination.
When the concentration of isoprene in isopentane-isoprene-
isopentene mixtures has been determined in this manner, the
content of isopentenes (P) can be calculated according to the
formula P - a.Pl-b. P is the found total number of double
bonds in the mixture, b is the concentration of isoprene in
the mixture and a is the correction coefficient. In the method
according to Rosenmund a - 0,96 and in the method according
to Gallpern a = 1,04. All performed tests are exactly de-
scribed. During the elaboration of this method a short
article by Timofeyeva and collaborators (Reference 18) on the
same problem was published. In this article a correction co-
efficient is introduced in the final formula of the calcul-
ation which only takes into account the error produced by the
inexact bromination of isoprene.

75-1-23/26
Bromometric Methods of Determining Unsaturated Hydrocarbons in
Isopentane-Isoprene-Isoamylene Mixtures
There are 1 figure, 5 tables, and 21 references, 15 of
which are Slavic.
ASSOCIATION: Institute 'Por Organic Chemistry im. N.D. Zellnskiy, AS USSR,
Moscow fInstitut organicheskoy khimii im.
H.D.Zelinskogo AN SSSR, Moskva)
SUBMITTED: April 8, 1957
AVAILABLE: Library of Congress
1. Hydrocarbons - Determination
Card 5/5

50)
AUTHORS: Zhukhovitskiy, A. A., Kazanskiy, B. A., SOY/2o-123-6-22/50
_Turkel'taub, N. M
Academician, St_er1izD_Y4__Q,__D. 1.
TITLE: Chromatographic Analysis of C Hydrocarbon Mixtures (Khronato-
gral'icheskiy analiz smesey ugievodorodov sostava C 5)
I@ERIODICAL: Doklaady Akademii nauk SSSR, 1956@ Vol 123, Nr 6,
PP 1037 - 1o4o (USSR)
ARSTRACT: The purpoze of the precent paper is the elaboration of a
quick and sufficiently simple method of the quantitative
analysis of isopent--iie-isoprene-isoamylene mixtures, Such
mixtures are forzed on dehydrogenation of isopentane into
isoanylenes and isoprene, Their analysis was complicated
and required much time (Refs 1-4). The authors successfully
used a combination of two chrornatoj;raphic methods: the
partition chromutography (Ref 5) and the "chromathermography"
(Ref 6). The methods were worked out on pure individual
hydrocarbons and on their artificial mixtures. The universal
"chronathermograph" was used for the analysis (Ref 7). Alu-
Card 113 minum oxide and diatomite impreCnatel tith dibutyl-phthalate

C!:ro--?--to&,raphic Analysis of C5Fydrocarbon @'Iixt!::-es S2V/
(2@@-43 by weig,it) served as corbents, The rendings on the
apparatus were automatically recorded by the patentiometer
EPP-09 . The results of the experi-ients with the cooperation
of A. 1. Karymova and P. S. Pavlova) are given in tables 1
and 2. Fi,-,ure la shows the separition of a conplex artificial
mixture Ur 18 of C 5- hydrocarbons. The c.iro,iatogrrr% shows
a distinct separation of all hydrocaibano except isopentane
and 3-met'iy1butene-1. Thin binary nixture was separated
with reopect to aluninum oxide it-in;, "chronathermog-r-aphy"
(Fig 2). The results were of s,-,.ti.,3factory accuracy. The deci.-
phering of the initial citrve is of considerable im,,,)rt-,ince
in analyses of this ty@e. V,@rious methods are used for this
purpose (Refs 8,9). Tnero :ire cases of an incomplete separa-
tion of the components of the lixture. A nothod. of calcula-
tion for t,',,e solution of this question(Ref 11) is sut-,-'ected.
Fi,.,,rures laand lb show t!-.e a:)-.1ioation of "chro-natoeraphy"
to the investigation of the @ehydrogenation products of
inopentane. The mentione(! universal apparatus can also be
Card 2/5 used for the deter-Mination of t.;-,e purity of hydrocarbons.

Chro-@r_to@,r!.-.phic An;,!.yris of C5Hydrocarbon !iixtures S9V/2o-1-3-6-22/5o
There are 2 figures, 2 tables, and 11 references, 10 of which
are Soviet.
ASSOCIATION. Institut organicheskoy khimii im. N. D. Zelinokogo Akademii
nauk SSSR ( Inatituto of Organic Chemistry imeni N. D. Zelinskiy,
Academy of Sciences USSR) Vaesoynznyy nauchno-iasledovatel'skiy
geologorazvedochnyy neftyanoy institut (All-Union Scientific
Research Institute for Geological Prospecting of Petroleum)
SUBMITTED: October 20, 1958
Card 3/3

S/595/60/000/000/006/ol'i
E196/E435
AUTHORS, Kazanskiy, B,A.. Sterli..gov, 0,D.. Belen'kaya. A P
Kondrat@yeva, G,f@_,
TITLE@ Catalytic dehydrogenation of isopentane
SOURCE: Vsesoyuznoye soveshchaniye po khimicheskoy pererabotke
neftyanykh uglevodorodov v poluprodukty dlya sinteza
volokon i plasticheskikh mass, Baku, 1957, Baku, rLd,
vo AN Azerb.SSR, 1960, 207-218
TEXT. Due to the lack of published information, the
authors investigated the process of dehydrogenation of isopentane
which yields as the internediate product isoamylenes, and. as the
final product, isoprene, the monomer of synthetic rubber. The
chrome-alumina catalyst K-544 was used, This catalyst, developed
by M_ N. Marushkin of IOKh AN SSSR, proved suitable for dehydro-
genation of n-butane and propane; it is highly active chemically
,h mechanical strength,
and has a hig All experiments were
conducted in the following manneri fresh or reactivated catalyst
in portions of 20 CM3 was heated in a quartz tube to the reaction
temperature in a current of air, The air was then purged by
nitrogen and isopentane was introduced in the tube, The liquid
Card 1/5

Catalytic dehydrogena Lion S/595/60/000/000/006/014
g196/L7435
reaction products were condensed by cooling with solid carbon
dioxide. noncondenstbles were collected in a Sasholder., The
unsaturated hydrocarbons in the condensate were estimated
bromometrically by the Rosenmund and Halpern methods, isoprene wa5
separately determined by weighing its adduct with maleic anhydride
or colorimetrically by the method of R, F- Robey and H,V.Wlese The
catalyst was regenerated after each run by passing a current of air
for one hour at the reaction temperature, Exper-,ments have shown
that during hourly working cycles in the temperature range )00 to
-1750C and that of space velocities 0,3 to 4@2 hr')@ the activity
of the catnlyst increaser] w-i th tempera ture , reaching a maximum at
5500C, maintained independently of the space velocity in the ranye
0.7 to 2,6 hr-1, Under those conditions tho- catalysa'te frui"
isopentane contained up to 58%, of unsaturated hydrozat-bons ' the
yield of the latter being 45 to 49% on tot-@-I isopentane and 70 to
90yo on the decomposed isopentane. The prodiictivity of' the
catalyst sharply increased with temppratiire. i-eaching the
optimum Ivalue. about 700 g C 5H 10 1014'khr at 55CC and si-ce
2@6 hr^ rhu-5 550^'C was the best, of thi@i
Card 2/5

S/595/60/000/uoo/006/0@4
Catalytic dehydrogenation E196/E435
Vis
The noncondensible gas7found to consist largely of hydrog-@,n s-il'h
some methane, The liquid products were analysed for th-r
individual unsaturated components by means of gas chromatography
and light scattering,#J-py-esults are given in Table V Analytical
difficulties in the estimation of the unsaturated componE-nt5 by
means of the Raman scattering syectra are diacuBied, They aris-
from the fact that the 1640 cm- line of isoprene is 12 time, mor,@-
intensive than the 1642 cm-'l line of 3@methylbutone 1, Th-
masking effect of isoprene is therefore -very strong and it teni-
to affect even the 1651 cm-1 line of 2-methylbutene-.l, In th-r
chemical determination of total unsaturation of the zataly6ate,
the Rosenmund method was found to give high values while the.
Halpern method gave low values. The correction far-tors whizh
had to be applied were 0.96 and 1.04 respectively, A,@,ademi,--iane
N.D.Zelinskiy, A.A.Balandin, B.A.Kazanskiy, Corresponding Member
AS USSR N.I.Shuykin, Yu,G.Mamedaliyev as well as V.T,Aleksanyan,
Kh.Sterin of Komissiya po spektroskopii AN SSSR (Commission on
Spectroscopy AS USSR) and Candidate of Chemical Sciences, Head of
Gazovaya laboratoriya (Gas Laboratory) of VNIGNI MNP SSSR aze
mentioned in the paper, There are 9 figures,, 6 tables and
Card 3/7

S/595/6o/000/000/006/oi4
Catalytic dehydrogenation ,, E196/E435
4 references, 3 Soviet-bloc and I non--Soviet, blo,., The reference V
to an English language publication reads as followsi
Ref.4.- Robey R.F, Wiese H,V. Analyt, Chem.,, 20, 1948 931
Card 4/5

Catalytic dehydrogenation
S/595/60/0001/000/006/oi4
E196/E435
Unsaturated components in catalysate W1W Tabl4:- I
Fraction 20 -38" 500-' 525' 550*
Total unsaturation 18@6 i 41,6 52,2
Isoprene 0.4
1.5
4@?-
2-methylbutene-.2 10 15 20/25-
2--methylbutene-l 5 15 15/30;@
3-methylbutene--l 3 3 -5/35;z

The analysis was carried oxit before separation (if dienes
in the friction 20-380,
Card 5/5

Ei/079/60/030/011/018/026
BOOYBO55
AUTHORS: Eydus, Ya. T. , Puzitskiy, K. V. , and StRrjjAZ*T_&-___Mr.
TITLE: Acid-catalyzed Synthesis of Eaters and Other Derivatives of
Carboxylic Acids From Carbon Monoxide, Olefins, and Compounds
Capable of koylation. IV. Carbomethoxylation of imylenes of
Different Structures
PERIODICALs Zhurnal obohohey khimii, 1960, Vol- 30, No. 11, PP. 3799-3802
TEXT: The present publication in an investigation on the oarbomethoxyla-
tion of the following isomeric amylenes by a method developed by the au-
thors in earlier studies (Refe- 1-4), 1-pentene, 3-methyl 1-butens, 2-nothyl
1-butene, and 2-methyl 2-butene. Am in the earlier papers (Refs. 1-4), the
reaction of the olefin, carbon monoxide and catalyst (concentrated H SO
2 4
in the first stage ct'the reaction, which involves formation of acyl sulfuric
acid as intermediate, pgoceeded at an initial CO pressure of 80 atm and at
temperatures of 20 - 40 C. Addition of methanol to the reaction mixture
transforms the acyl sulfuric acid into its methyl eater in the second stage
Card 1/3

Acid-catalyzed Synthesis of Esters and Other S/C)79/60/030/011/018/026
Derivatives of Carboxylic Acids From Carbon BO01/BO55
Monoxide, Olefine, and Compounds Capable of
Acylation. IV. Carbomethoxylation of Amylenea
of Different Structures
of the reaction. Xethyl esters were obtained from 1-pentene in 54%
yield, and from the branched amylenes in 64 - 69% yields, as calculated
for initial olefin. 2-Mothyl 2-butene gave the highest yield (69%).
Mothyl-1,1-dimethyl butyrate was obtained as the main reaction product
from all isomeric amylenes. The mixture of esters from 1-pentene contained
50-5% of this ester, that from 3-methyl 1-but*ne 61%g from 2-methyl 1-butozo
45%, and from 2-methyl 2-butene 35%. The structures of the remaining reac-
tion products varied according to whether the initial compound had been
n-amylene or branched amylene. In analogy to the results obtained with
1-hexene and 1-heptene, I-pentene yielded methyl-l-ethyl butyrate, as
second reaction product, which constituted 27-5% of the ester mixture ob-
tained. Methyl-l-ethyl butyrate was not detected among the reaction prod-
ucts from branched amylenes, which are partly transformed to methyl-tri-
methyl acetate (4 - 10%), 1,1-dimethyl valeric acid (0 - 5%), and higher
acids (30 - 5*. There are 1 figure, 2 tables, and 16 references;
Car,d 2/ 3

Acid-catalyzed Synthesis of Esters and Other S/079/60/030/011/018/026
Derivatives of Carboxylic Acids From Carbon B001/B055
Monoxide, Olefins, and Compounds Capable of
Acylation. IV. Carbomethoxylation of Amylenes
of Different Structures
6 Soviet, 4 US, 1 British, 3 German, 1 Italian, and I French.
ASSOCIATION: Institut organicheskoy khimii Akademii nauk SSSR (Institute
of Organic Chemistry of the Academy of Sciences USSR)
SUBMITTED: December 18, 1959
Card 3/3

STERIN, Kh.Ye.; ALEKSANYAN, V,T@@ UKHOLIN, S.A.; BRAGIN5, O.V..'
GAVRIIDVA, A,Yq.@ ZOTOIVA, S.V.,- LIBEF(MAN, A.L.; MIKRAYLOVA, Ye.k.
SMIRIIOVA, E.N,, STERLIGQT,_Q@@- KAZANSKIY, B*A*
Raman ?pe-:1ra of some tri., and tetraalkylbenzBnes and condensed
aromatic hyd.-ocarbona. Izv. An SSSR. Otdakhim.nauk no.8:1444-
1450 Ag 14-1. (MIRA 14.8)
1. Yxm@eBiya po spektroskopii AN SSSR i ine"Itut organicheskoy
khiali im. N.D. Zelinekogo AN SSSR.
(Benzene-,Spectra)
(T -
-Vdromrbone- -Spectra. I

25393 s/,-,r_c/6,./034/0G2/ /ol3/025
29
;LIDO . O*D.t Been'ka'fSv A.P., Eyd",
.1S
AUTHORSS ya.T. yiene mixtures
TITLE$ A
pERIODICALt 34, 1166-:15b.
w 1% fA
e
f f
Y -
TEXTz fr-Y
Y@ .-Jiz.e
. i@ -,
1_4 i L AZY-
yield by
gasc.-
The main
msr-,- h. u 1960))
carboxyl'- ane M p
f@-,r I I W, ), 41-1. 19,
'13 r @ .
lenes are tRet OKJ.
Ir. I , a 4 from
line or Y. Y
'r, t ji Sr, a-d
the prese, . V _d C1
9
ule.r,ps With 2.hj mp',hy' cettr -,f oi@k_di-
single Fjz wav%
served that th@' M96!,"
Card 1/

5 3 9.^-
S //C 6 01/6. I/C" 4 //"'C 2 /013102 5
Preparatic_,i rf AO= 7'/A 12 9
methylbutyri,, a-ii. T,'oA,.3 was- alLsz- t;: te m3.iL re-
action f;,,-m a, mlx-,,@:!-a @,f dEylenes in @-Ae ;rsL-ent t@xcez-@@mmen--? r-m-
talyzates :@f d-@.hyiz@:g-ratfc.x;J -_--fertane, ard r-pertare., as well as
the pen tane-amy '-f thArmal. cc@acic_IrAg 1@1,cduct!? .-f g--ig D11 (Tab.1)
were carb-_xymetty.'Et;@1. hi, EL I tr. e aL d t 4 6 r@ t f f i,at i r r. C f th e O'@ 4-L e d
eaters were carried out In doss@ribed 92rea4y in the @revicua
paper (Ref '4). az.,i -)29 clbtainsd r6sults -er@ :L= Table
Tbere i:@ 1 figurp ,
2,3. 5 ,ab'lez) ar-d 14 refersnceat 6 Scviet-11c.; and 8
non-Soviet-t!.-c. Three I-f the Englilab-language references read ae fc1lowes
F.C. Whitmcre, F.A. Karnat:, j. Am. Chem4 Sc--.., 6n, 42533 (19,148); D.V.N.
Hardy, J. Chem. Sll--., 464 (19.`PJ), J.M. Hc@ltert, J. Am. Pharm. A?srr-.. Sci.
Ed., 35, 315 @1194@)-
SUBMITTEDs March 14, 1960
Card 2/5

,D._; ROZHKOVA, M.I.
P--rARLIGUI --0
Continuous isomerization of 2-motbyl-2-butene and 2-metbyl-l-
butene in to 3-methyl-l-butene. Neftekhimila 2 no.3:288-290
MY-Je 162. (KRA 15:8)
1. Institut organicheskoy khimii AN SSSR imeni Zelinskogo.
(Butene) (Isomerization)

S/2o4/62/002/004/003/019
E071/E433
,%UT14014S; Kazanskiy, B.A., Dorogochinskiy, A.Z,t'S.terligov O.D#t
:Z=Znz-:@
Lyuter, A.V., Dmitriyevskiy, M.L., Nazaeov, F,5.
TITLE; Dehydrogenation of i3opentane into i3oamylenes on an
alumochromopota3sium catalyst
PERIODICAL: Neftekhimiya, v.2, no.4, 1962, 448-456
TEXT: A systematic study of the process of dehydrogenatiOn of
isopentane into isoamylenes under conditlov.3 of a stationary and
34 moving layer of granulated catalyst K-544 was carried out on
re experimental installations of Groz NII. Tests on the stationary
co@ layer were carried out on a laboratory and.an enlarged
to installation. The reactors with a stationary layer of the
for catalyst were of the capacity of 40 and.506 cm3 respectively.
Ca t. Tests in the moving layer were made in a co-current continuous.
pilot plant with a reactor (4 litres) and a regenerator (4-7 litres).
'Isstj The volume of the catalyst - 35 litres, throughput - about
100 litres/day, the velocity of circulation of the catalyst
up to 16-litre3/hour. The analyses of the reaction products were
made by chromatographic and other chemical methods. The influence
CQ-rd of the temperature, volume velocity and rate of recirculation of
Card 1/2
U--
)CI '*,Ka nt C

STERLIGOV , 0. D, ; BELENIMLI . A @ P.
Ef Vect of the composition of alumimam-chroaim-potassium oxide
catalysts on their activity in dehydrogenation of isopentane .
Izv. SSSR. Otd.khim.nauk no.5:8M-805 14Y 162. 15:6)
1. Institut organizheskoy khimii im. N.D.Zelinskogo PJ" SSSR.
(Catalysts) (Dehydrogenation) (Butane)

GOIIIKBMG I M.G.; GAVRILOVA, A.Ye.; STERLIGOV., O.D.; RcZIMOVA, X.I.
Thermal polymerization of pentenes at hiCh pressures. Izv.AN SSSR.
Otd.khim.nauk no.8:1458-1463 Ag 162. CaPA 15:8)
1. Institut organicheskoy khimii. im. N.D.Zelirwkogo All &WR.
(Pentene) (Polymerization)

KAZANSKIY, B.A.; LICROGOCHINSKIY, A.,%; @@'AAILIGU, -0.-D,; LYUTER, A.V.;
U41TRIY?,VSKIY, M.L.; NAZAROVA, M.P.; RE 41VIASIIVlLl , A.N.
'Studying the dehydrogenation of isopentane on K-544 and K-5
finely divided catalysts. Trudy GrozNII no. 15:241-253 163.
(MIRA 17:5)

rinz c Z. a r e S
5 n(@.3: -1 -7 1
neftyanoy
L 4 t

ISTERL160`1) O.D.- Y-1,1:;EYEV, IN.A.
-11-
Dchydrogenation of isopentane in reacLor@: of various
Neftekhimia 4 no-3:391-398 MJ-Je '64.
Development of an aliuiina-chrome-potassium catalyrt in the die-
hydrogenation of isopentane. lbid.:399--4C5
(MIRA 18:2)
1. Institut organlicheskoy k1lindi AN SS'SIR Im. N.D.Z(Ilnskogo.

I IOf il-,oi-ent'are c-ff,@r!t of u ii-,al i Neftei-nimla no.4:
N. *1 533
nichookoy khimii im. I _,. Zeiinorogo AL PL.

L 34004-65 EWT(m)/EPF(c)/E#W(j) Pc..4/Pr-4 RM
ACCESSION NR: AP5006073 S/0204/65/005/001/0010/0016
AUTHOR: Sierligov, 04 D.; Yellseyevs No At
TITIZ: Dehydrogenation o;-Isopei tane on- alumina-chmata -potassium -axide
The effect of the chr- -- 0k1de content-in the cataly t
SOURCE: Neftekhtmiya, v. 5, no. 1, 1965, 10-16
TOPIC TAGS: isopentane dehydrogenation, catalytic d6hydrogenation, alumina cat&-,
lyst, chromium oxide catalyst, hydrocarbon isomeritation
ABSTRACT: The effect of Cr203 contents of 1-40 wt,% itt K20-activated alumina-
chromia catalysts on the dehydrogenation and skeletal isomerization of Isopentane
wan experimentally studied as part of research on the activity and regeneration
of such catalysts. Development of catulyst activity with time and formation of'
isopenta nee 2isoprene v normal C.-hydrocarbon; and of C-C hydrocarbons a
sured at 550C, atmospheric pressure and a f ow rate cl I)hre over a con'sIttmea
volume (25 cc) of catalyst, whose bulk density increased and whose specific sur-
face decreased approximately two-fold with increasins; Cr203 concentration from I
to 30%. The fresh and oxidized catalysts reached mw:im= activity most rapidly
at a 20% Cr203 content, maximi yields of isopentaneo (44.7 wt.%) and normal C5
Card 1/2

L 34004-65
1'-ACCZSSION NR.
Ap5006073-
@
ene-
hydrocarbons were obtained at-15 wt.% Cr2O3, and the immimm amount of isoo
(2.1 wt.%) was formed over a catalyst containing 10% ft. 0 Coking was most in-
3
g
;
e
Leld of gaseous pro-
tenaLve with a catalyst containing 20% Cr 0 eress t
2 3, wh
ducts was little affected by the chromium content. The rate of development to
maximum activity was also shown to increase with the hydration of the catalyst
surface. The analysis of aqueous catalyst extracts indicated the presence of
Cr03 in oxidized catalysts and the formation of basic and acidic acti@e centers
during the hydrogenation process, skeletal Lsomerftat'Lon proceeding primarily on
acid centers. "The authors thank V. 1. B060molov for determining the specific
catalyst surface area." Orig. art. has: 2 tablei, 4 figures and 2 formulas.
ASSOCIMON., Institut organLeheakoy khImiL im. N. D. ZelLnekogo, AN SSSR
ganic chemistry institute# AN SSSR)
SUBMTTED: 14may64 ENMO. 00 SUB CODE: 0C
NO REP SOV: 010 OTHER: 009.

Card 2/2

YJiODAKCVp Yu.S.; MINACHEV, Kh.M.; STERLIGOVj, O.D.
Kinetics of the catalytic dehydrogenation of bviLane W
butylenes. Dvkl. AN SSSR 165 no.2:344-346 N 165.
(MIRA 18"10
1, Institut organiaheskoy kbinii im. N.D. Zelinekogo A.@ -'"tSR@
Submitted Aporil 12, 1965,

of@ thf, nature or altiminim oxIde on thf: propertle.] of
Till jrt aum III I Il- cilromi U.-n-po ta s si urr. oxido catOyst. for loopentane
d@!,hydrovenat! oil. fleftekhImlia 5 no.6:&19-.814 N-D 165.
OKIRA 19:2)
1. In-,--tatot organlcheskoy khimli impri Zelinsko.,7c AN SSSR.
-i!b:., d Nov . 2 P IC1,61'.

Alo'. tiw, brc.,ught C,:I' Prof .--te?m. obr. 20
(111IRA 16'.7)
-!-7 -63.
na I c
jirofessLo 1 n
'I Aa

AB.-JuNWICH, A.D., kam':. te.'Jin. nauk; AVIO11U, R.F., k,;n,;. tckhn.
nauk; KAPL.-T, G.A., inzll.-ekonoi:ist; LEVII-l, S.P., inzh.-
zer-leustroitell; LISTENWRT, F.M., !.-nc*.. f;eogr. rauk;
SANY;01.1, Yp.V., kan(i. tekhn. nauk; kLnd.
arkli'tell,..; @,OLNVITKO, kan6. arr`Yt..; .,97&-'-.LIGOV V.D.,
kand. arkht.; F.*.Lh',YFV, V.G., inzh.;
BbTuzC'Vj., V.P.; GLABIT;;., N.K.; GOLIAD51,T1,11, A.Y.;
D1N[AjTO'V-47jjy, V.S.; KAFLAF, G.L.; MOTU`, N.A.; i."'E!"ILIIII
G.I.; @AJRIAKUV, N.Yv., red.; KOVNITEYETS, Mi., red. izd-va;
GOLOMNA, A.A., tekhn. red.
(Regional planning of cconomic adninistrative regionsp
industrial regions and centers; 1.1nnning guidelliaionnaia
planirovka ekonor.iclesl:ikh a&lnistr,-tiirnykh raionov, pro-
r,yohlennyl:h raionov i uzlov; rukovodstvo po procktiravaniiu.
Pod redX.IA.burlakova. Moskva, Gosstroiizdat, 1962. 266 p.
WIRA 15: 10)
1. Akador.',Ya stroitellstvL i arkhitektury SSSR. Institut gra-
605trOltell---tva i raiormoi planirovki. 2. Zamr-titell direk-
tora po muchnoy rabote 1:auchno-issleclovatellskogo instituta
gradostroitell5tva i rayonnoy planiroylci (for Wrlakov).
3. Fauchno-issledoyntellakiy institut g.-ndostroitellstva I
rayonnoy planiroirki (for Butuzova, lulabina, Golldshteyn,
Dcr@yanovzs'-J.y, Ka,,Ian, Fedotova, TScytlin).
(J@egional plnnnAn,-,-)

STERLlGOV, Y.F.
(@iestiana und proble= on the topic Tropertles of solid bodies. " Yiz. r
ahkole 13 no.5:77 3-0 153. (ML" 6:8 )
1. 569-ya arednyaya shkola, Moscow. (Solids)

SERGZYEV, Ivan Ivanovich; SMMYARSKIY, Mikhail Valentinovich; STRUIGOV, Y.L.,
inzh.-kapitan, red.; BABOCHKIN, A.T., teklin.red.
(Textbook for electricians] Uchebnoe posobia alaktromekhanika.
Koakvs. ToenAzd-vo N-va obor. SSSR, 1958. 284 p. (MIRA 12:3)
(Electric engineering)

PATROV. Yiktor Pavlovich; SOCHIYKO, Arkadiy Arkad'yevich; SOMLIGOT. -,__
Y.L., inzh.-nayor, red.; ZUDIKA, K.P.. tekhn.red.
[Rocket guidance] Upravlenie raketami. Moskva, Voen.izd-vo
M-va obor.S=. 1959. 207 P. (MIRA 13:2)
(Guided missiles)

DIKIT, Alakeandr Danilovich. kand.takhn.nauk; SOLDATOV, Ivan Andreyevich.
Prinimal uchastiye KUATOVXER, I.Ye., kand,tekhn.nauk. STEMIGOT,
T.L.. inzh.-mayor, red.: SRUNIS, 11J., takhn,red, -
ERadio transmitting devices] Peredatchiki rediotekhnichookikh
aradetv. Moskva, Voen.izd-vo X-va obor.SSSR, 1960. 367 p.
(MIRA 13:7)
(Radio. Shortwave--Transmitters and transmission)

PARFENOV, VaBiliy Aleksandrovich, kand.takhn.nauk; STERLIGOVp V,L.p
inzb.-mayorp red.j ZUDINAp M.P,v tekhn.red. -.-I.-
[Returning from Bpacel Vozvrashchenie Iz kosmosa. Moskyat
Voen,izd-vo H-va, obor.SSSRt 1961. 67 p.
(space flight) (KIRA .14%6)

VI Still EVETSKIY, A:Leksandr 1111ch; SERGIYENKO, Ivan Stepanovich; @T]@R@Ms -
V.L., lnzhener-mayorp red.; KRASAVINA, A.M.p tekbn. red*
[Paratetron; new switching elements]Paranetron; novye perekliuchaiushchie
elementy. Yoskva, Voen. izd-vo M-va obor. SSSR, 1961. 66 p.
(MIRA 14:8)
(Electronic digtta@ computers) (Switching theory)

INASHEITKO, Ivan Dmitriyevich; STE,-LIGOV, V..L,,., recl.; MASLOVA, N.Ya.,
teklm. red.
(Radio mvigation method s ]Radionavigatsiia. Moskva, Voonizdat,
1962. 75 p. (MIRA 15: 8)
(Radio in navigation)

I-',l.*.TOVO Gennadiy Dritriyevich; GORBACMV, Viktor Fetrovich;
STEIILIGOV, V.L., red.; KRASAVIIIA, A.14.0 tekhn, red,
[Radar systems with active response] Radiolokatsionnye sisteny s
aktivnym otvetor.. Moskva, Voenizdat, 1962. 113 p.
UlIRA 15:5)
(Radar)

i,ViSUKOV, Filipp Ivnnovich,, I-AKSMOV, Matvey Vasillyovich;
STERLIGOV, V.L., red.; CIIAPAYEVA, R.I., tekhn. red.
(Radio-telemetry]Radiotelemetriia. Moskva, Voenizdat, 1962.
183 P. (VTIRA 15: 8)
(Telemetering)

POKHOVSKIY, G.I.; SLABKIY, L.I.; STERLIGOV, V.L., red.;
CHAPAYEVA , R.I., tekhn. *- - - -
[Physics in technology] Fizika v tekhnike. Moskva,
Voenizdnt, 1963. 83 P. (MIRA 161ll)
(Physics) (Technology)

YUHIYEV, E.Yu.; 6TKUlGOV., V.-L., red.; VEDLIKUVA, A.D.., tekhn.red.
(aadio communications with space rockets] Radiosviazl s
kosmicheskiLi raketami. Moskva., Vocnizdat, 1963. 77 p.

KUROTKIN, Vladimir Ivnnovich, inzh.-podpolkovnik; STERLIGOV Vladimir
Laoilidovich insh.-mayor; SHIRYAYRV, N.P.,
mayor,
@Knfmw"-7. ., tekhn. red.
(Homing guidance of rockets] Samonavedenie raket. Moskva,.
Voenizdat, 1963. 87 p. (MIRA 160)
(Guided missiles--Guidance systems)

PCLISAR, G.L.; STERLIGOV, V.L.J, red.; SOLOMONIK, R.L., tekhn. red.
Cllodeling]Modelirovanie. Moskva, Voenizdat, 1963. 119 p.
(MIRA 16:10)
(Electromechanical analogies) (Electronic computers)
(Similitude,Theory of)

PETROV, Viktor Pavlovich; SOCHIVKO, Arkadiy Arkad'yevich; STLRLW.OY,.
V.L., red.; PERETRPHINA, G.F., red.; KOKINA, N.N., tekhn.
__ 4
re .
(Rocket control] Upravlenie raketami. Izd.2., ispr. i dop.
Moskva, Voenizdat, 1963. 263 P. (MIRA 16:4)
(Rockets (Ordnance))-Controls)
A

@ .@ 1, !@. ; 'i . @!i., @. , @. i I- I i v. I r I. i i@ i - @-, - @ -, " , "' . 1, . p I " !d .
r
L i.,i @le @ -o it, cut e- " @ @-- :@ -3 , c- :. *, he ea r4,-.'I a r@@ ur@le r .T. I e r ';
111,le -y- -v Rosmose , na zemde i ycKl vod 11-cer-
- I t, ci. !-:c.skva) v
izdatp 102 1). (YIHA 17.6)

CHERNY311, G. I.; STERLIGOV) V. V.; VAYNS11TEYN, 1. L.; RA7HFNOV, M. M.
-f- - -- -11.:: 11 . - I
Intensifying the rate of open-hearth smelting with the help of
a new fuel burning device. Izv.vys. ucheb. zav.; chern.met.
7 no. 4:146-150 164. (MIRA 17:5)
1. Sibir3kiy metallurgicheskiy institut.

1. STERLTGOVA, M.
2. USSR (600)
7. "Rays that Kill Microbes. (Bactericidal Lamps and Their Ipplication)",
Tekhnika Molodezhi, No. 7, 1951, p 19.
9. Mikrobiologiya.Vol XXI, Issue 1, Moscow, Jan-Feb 1952, pp 121-132, Unclassified

jj jjh 1@52. Uncl.

STS- LTC;V,'A, 1'.
Fol-i7rti-m
,rrp.nsfr:-n-@--tion of 1-it-lit. Telkh. molod. 20 No. 4, 195"1
I'onthl 1121 of Pi:,sAm Acces-Aons, Library of Congress, July 1952. LP14CLASSIFIED.

1. ST7RLIGOVA, Eng. M.
2. USSR (600)
4. Rerraction
7. Pofraction of light. Takh. molod. 20 no. 12, 1952.
9. Monthly Liats of Russiankocessi -y of Congress, March 1953, Unclassified.
- @@ Librar -

STIBLIGOVA. M., inshener.
Interference of light. Tekh.molod. 22 no.l.*15-16 Ja 154. (XLRA 7:1)
(Interference (Light)

Sterligova, M., inzhener.
-S-111.1-1 1,
Daylight without the sun. Takh.mol. 22 no.8:30-31 Ag 154.0"A 7:8)
(Fluorescent lighting)

STERLIGOVA, M. inzhener.
Rectangular picture tube. Tekh.mol.24 no.8:14-16.39 Ag 156.
(Television--Picture tubes) 01IRA 9:9)

Cu i civet U'd t II tou 3
Ni". 3 3
ova
iatju.,?naa of Copper a;id Margoncho at, thet
crowiti, I)Pvelopmeent a-j@ci YitAld uC Ptunpkins
Tomatatm
0: ;3b. :-auchn. r0'00fl' P6tr-!:@avodt',ogo un-tall
L.
Vn), 3, 126-145
-,h,:! reaul-z.5 &re given tit: euporlment.4 cox@,nvr,-
tod at the Chalr of P-lar4t Fshys.1clogy in 19552
o nd I -) @% @'j ,The oxpurim&atal patth i-md a a-ine-
ral soil; the oxparimenta wora mado ugh-Irtj%t
a Wtclcgraund at fertilization, where fu*-,.]
mineral furtilizar UNPK) and manure were
added to thu- soil. The fertilization of the
pumpkins and tomatneo with mir-ronutritints
ttn.b meta-Leved by v-,%rioui@ usethods: applicatic-i-I
of' tlj,@ miuronutriants directly into the floilt
C @,Ra 1/3

CHERNIGOVSKIY, Ye., inzh.; STERLIK, I., inzh.
Electric heaters for oil dispensers. Avt.transp. 40 no.9t25-26
S 162. (WRA 15:9)
1. Gruzovoy avtopark No.25 Glavkiyevavtotransa.
(Electric heating)

TSFASP B.S., dot:sent, kand.tekhn.nauk; STEERLIKOV, F.F., student
Increasing the range and precision of movement regulation in
universal machine tools used in lot production. Sbor.dokl.
Stud.nauch.ob-va Fak.mekh.sell.Kuib.sellkhoz.inst.no.1:51-60
162. (MIRA 17:5)
1. Kuyb.vshevskiy sellskokhozyaystvennyy institut.

STERLIKOV, F.F., stucent; YEUIMIN, A.V., kand.tekhn.nauk, starshly
prepodavatell, nauchnyy rukavoditeltraboty
Self-centering hinged dovetail remover. Sbor.dokl.Stud.nauch.
ob-va Fak.mekh.sell. Kuib.sellkhoz.inst. no. 1:142-146 162.
(JIRA 17:5)
1. Kuybyshevskiy sellskokhozyaystvennyy inistitut.

STMIKOV. I.I., m4ster kolodtoev blyuminga
Operation of regenerator soaking pits for blooming wills with
liquid slag repoval. Metallurg 5 no. 12:26-29 D 16o.
(HIRA 13:11)
1. Magnitogorskiy metallurgicheakiy kombinat.
(Rolling mills-Rquipment and supplies)
(Furnaces. Heating)

L 4103-2-65 EVIr (d)/E','IT (M)/E';,'P WA-2 EM
ACCESSION NRt APS008577
AUTHORSs Zuyov, M A 1 Razin 0. M.; Krylov, V. M.1 Volkoy, A. F.; Timshimu. I
P.1 Gklov, S. A.) losmasov, V. is. ; Hirolyuboy, 0. P.
TITLEt Tas stand for creating impact overloads. Class 62, No. 169407
SOURGEt Byulleten' izobroterAy i tovarnykh snakov, no. 6p 1965" W
TOPIC TAM impact testing
ABSTRACT iOki This Author Certificate presents a test stand for creating imact
overload.-il The stand contains a truss with controlling cables, a hoisting
dovice, a platform for the investigated object, a cable with a suspension syst41%
a cut-off mechanism, a braking mechanism, shock absorbers, and instruments for
moazurinr, the platform drop rate. To increase the safety of the experiment and
to exclude the effect of the prescribed height on the free fan of the platform,
the stand is provided with a contactlese mechanism for setting the height (aso
Fig. 1 on the Enclosure). It consist* of a transmitting selayn corimted br a
flexible shaft to the shaft of an electric tackle drum, a receiving solos placed
in the frame of the mechanism, mA a ambarAss reductor. L setting InAlester Vab
a knob " contact, a @34din indicator with a contact, a bei4bt Indleatm s"Ies,
Ci,d 113

L 41032-65
ACCSSSION KRi
AP5MS77
a stop relay am oowmtod in the aftmUs otwtw siradt of the 41066rim
tackle. Orig. art. h"s I diWam.
ASSOCUTIONs none
SULWTED# 02J&A CM31 MB
NO RW SOV s 000 arms 000
c.rd 2/3

L 38265-65 EWT(1)/EPR/EKA(m)_2/EyjA(h) Ps-4/Peb WW
ACCESSION NR: AP500`7450 S/0286/65/000/004/lXrn/0073
AUTHORSI Sterlikov, V. P.; Roy,, E. V.1 Chuchkin, Vs G.; Rozhdostvenski7, V, 1,
TITLE: Thermal flowmeter for small flow rates of liquid. Class 42, No. 168M
SOURCE: Byullaten' izobretoniy i tovarnykh znakov, rio, 4. 1965# 72-73
TOPIC TAGS: liquid flowmeterP
ABSTRACT: This Author Oertificate presents a thermal flowmeter for small flow
rates of liquid. The device contains a thermocouple with two junctions as the
sensing element, a measuring tube passing through the two-chambered case of a
thermostated detector, and two thermostats maintaining a temperature drop between
the detector chambers, To increase the accuracy of x2easurement, the themo-
couple is placed along the axis of the measuring tubo. Both junctions are placed
in one detector chamber (see Fig. I on the Enclbsure). To increase the sensi-
tivity of the device by creating an equilibrium tempirature field in ae region
of the detector case., it is provided with additional chambers inside of which
are mounted perforated tubes, Orig. art, has: I dingram.
ASSOCIATION: none
SUBMITTEM 29Nov63 ENCL, 01 SUB CODE: IEj W,
NO REF SOV: 000 OTHERs OW
Card 3.4

BELKOV, S.F.; STERLIKOV, V.V.
Yaking larg@% separators by means of liquid metal drop forging.
Lit.proizv. no.2:8-9 F '60. (MIU- 13:5)
One casting) (Forging)

Fuel Abst.
Vol 14 No. 4
October 1953
Natural Solid
Fuels: Sources and
Properties
3012. 1ID7 DATA ON
DOMETS BASIN kND F.
JURASSIC DEFOSITS OF
-4
J" (Dokl. Akad, Nauk SSSR (Rep. Acad. Sci., U.S.SeR.),
21 Apr. 1953, vol. 1), (5), 929-932). (L).

__`@ I E lkx- ' P
'S_A&N@b.'P._; BnYANKIN, D.S. akademik.
Boundary of the Middle and Upper Jurassic in the Donets Basin. Dokl.AN
SSSR 90 no.5:867-868 Je '53. (MLHA 6:5)
1. Vseaoyuznyy neftyanoy nauchno-issladovatellskiy geologo-razvedochnyy
institut (for Sterlin). 2. Akademiya nauk SSSR (for Belyankin).
(Donets Basin--Geology, Stratigraphic)

-7- -- ' - -
/ =/A'\ L I A/ . r7
MIGACHEVA, Ye.Ye.; STERLIN, B.P.; O.BRUCHIV. V.A., ukademik.
Paleogoography of the Middle Sarmatian period in Moldavia. Dokl.AN SSSR
91 no.3:617-619 Jl '53. (MLRA 6;7)
1. Akademiya nauk 33SR (for Obruchey).
(Moldavia--ftleogeography) (Paleogeography--Noldavia)

-STERLIN-) N-4 Y-@
USSR/Geology
Card 1 1/1
Authors Sterlin, V. P.
Title Boundary between Triassic and Jurassic formations In the
Don Basin
Periodical Dokl. An SS.;R, 96, Ed. 4p 807 - 808, June 1954
Abstract The changes in the formation of deposits in the Don Basin
territory, which took place during the Jurassic and Tri-
assic periods, and are evident from the conversion of the
light colored Triassic deposits to the dark colored Jur-
a3sic deposIts, are discussed. Seven references.
Institution Ukrainian Section of the All-Union Petroleum Scientific-
Resear--th Geological Institute
Presented by: Academician S. 1. Mironov, March 26, 1954

USSR/Geology
Card 1/1 t Pub. 22 - 35/48
Autbors I Sterlin, B. P.
Title I 1h.ture of the joining of the Dnieper-Don depression and the Don fold-
Ing area
Periodical I Dok. AN 3SSR 97/5, 891-893, August 11, L954
Abstract t Stratigraphic and tectonic data on the -joining of the Dnieper-Don de-
pres3ion and the Dori River folding area in the Ukr-SSR. Six USSR re-
ferences (1937-1953). Diagram.
Institution : All-Union Scientific Research Petroleum Geological-Exploration Insti-
tute, Ukrainian Branch.
Presented by : Academician S. I. Mironov, April.10, 19154

STMIN, B.P.
Conditions of formation of the Upper Bath deposits In the north-
western Donate &@in. Dokl.AN SSSR 104 no-5:765-766 0 155.
(RUIA 9:2)
l0krainskeye otdeleniya vuenorusnogo nef tyanogo nauchno-ineledc-
vatellskogo geologo-rasvedochnogo inatituta. Prodstavleno akademi-
kom S.I.Mironovym.
(Donets Basin--Geoloa, Stratigraphic)