SCIENTIFIC ABSTRACT SHVARTSBERG, A.I. -

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001550330005-9
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: August 31, 2001
• Sequence Number: 5
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

KUZNETSOV, Yu.A.; SHVARMBER.G- A.I.
~ ~
Algorithm for calculating the optimal structure of the e*rgy
balance on an electronic computer taking into consideration
the conditions of gas consumption. Gaz. prom. 9 no.6sl5-19
164. (MIRA 17:8)

SHVARTSBJ:HB, I.Yu., kand.voyenno-morskikh nauk., kapite4 1-go ranga
Defende against ballistic missiles in foreign c9untries; from data
in the foreign pre so. Mor. sbor. 44 r-o.5:77-82 My 161.
(Ballistic migsileg)
(Great
(MIFLA 16:5)
(United States--Air defenseq)
Britain-Air defense&')

KUZNETSOV, Yu.A.; MAKAROV, A.A.; MELENTIYEV, L.A.; MER3,11KOV,
A.P.; NEKRASOV, A.S.; TSVETKOV, N.I.; KUZIV'ETSOV, Yu.A.;
MAKAROVA, A.S.; YLARFOV, V.G.; I-WJ-'--UROV, Yu.V.; VROV,
Yu.P.; K1hJLEV, L.S.; TMETKOVA, L.A.; VUTSE1011OVSKAYA,
G.V.; YEFIMOV, 11I.T.; UET"EIAL', G.B.; KIWIAYEV, V.A.;
i3ELYAYEV, L.S.; GAI,.I-" FAIRTELEV, B.G.; KAU101, L.A.;
LIOPO, T.N.; 3-VIRKUTIOV, U.N.; DRUMININ, I.P.;
KONOVALENKO, Z.P.; KHAI-111YANOVA, N.V.; SHVARTS~ERG, A.I.;
NIKONOV, A.P.; STARIKOV, L.A.; POPYRIN, L.S.; FSHRUCH11OV,
N.N.; THOSHINA, G.M.; CIIEL'TSOV, M.B.; SVETLOV, K.S.;
SUMAROKOV, S.V.; TAKAYSHVILI, M.K.; T01MACHEVA, N.I.;
KHASILEV, V.Ya.; KOSHELEV, A.A.; KUDINOVA, L.I., red.
[Methods for using electronic computers in the optimiza-
tion of power engineering calculations] Metody primeneniia
elektronno-vychislitellnykh mashin pri optinizatsii energe-
ticheskikh raschetov. Moskva, Nauka, 1964. 318 p.
(MIRA 17:11)
1. Akademiya nauk SSSR. Sibirskoye otdeleniye. Energetiche-
skiy institut. 2. Chlen-korresponuent Pli SSSR (for Melentlyev).

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USSR/Metals - Foundry, Platerials Aug 51
"On Send=etallic Mixtures," B. V. Shvaxtsberg,
Cand Tech Sci, Chelyabinsk Plant imeni. Kirov
"Litey Pro1z" No BY p 25
BrIer17 discusses core mixts made partly of metal
shavings- or shot and compares their compn and
properties -41th those of regular core sand and
magnesite. Cores for expts were made of cast-iron
chips, shot and powder, obtained from vaste after
grinding castings, with adcIn of nonmttallic ma-
terials such as sand, magnesite PoWder 3nd sulf ite-
cellulose liquor.
197779

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SHVARTSBY.RG, I-Ya.; SER IN, YU-M-
Rousehold kitchen range and combined boiler-range with a coisoon
firebox for solid fuel. Sbor. trud. NIIST no.4:146-154 160.
(MIRA 13:11)
(staves) (Boller*)

611VAXTSB&iG,, L.V.
Results of short-term reversible collapsotherapy. Zdrav. Kazakh.
21 no.5:53-54 161. (MLIA 15:2)
1. Iz tuborkulezroy bollnitsy g,,Temir-'Tau.
(FNLaICYrH

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SOV/137-59-1-510
Translation from: Referativnyy zhurnal. Metallurgiya, 1959, Nr 1, p 65 (USSR)
AUTHORS: Osipov, B. R., Chernin, V. N., Shvartsberg, M. B.
TITLE: Industrial Production of Titanium (Promyshlennoye proizvodstvo
titana)
PERIODICAL: V sb. - Legkiye metally. Nr 4. Leningrad, 1957, pp 105-108
ABSTRACT-. A description of the technique of Ti production by the magnesium-
reduction method,
M. M.
Card 1/1

GORBACIINVA, I.N.: VARMOVA, L.P.; MONIGH, N.Y.; POLYACHENKO, Y.M.; ROKANOTA,
A.B.; TULICHINSKAYA, L.S., SHVARTSBIRG, H.S.
Synthesia of substituted 1-benz7l-3.4-dihvdroisoquinolines. Zhur.
khim. 27 no.8:2276-2282 Ag 157. (NIaA 10:9)
1. Moskovskiy inatitut tonkoy khimichemkoy tekhnalogii.
Nainoline)

6. 2" A. N.. S~~
T.-Li. Sy.th..L. of 3-1-r.1 2o..=.m - LI.-4h-j-
PUICLIC&L.

'
A
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t
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f
71
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T.
.
t
i.l Pm*"ts ror t ha Frjd~ztlon
filch Poly Worc- which tock place in larcal.,11 erna 3.pt,zb.r
29tOntOber 2. 1958. 'he ran% Ito of the c.t.lytin synthesis
of 2.
dLxWthYI
bUt%d1
n
5 - ii - or au...r. or th
.

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t first a be
:
1. t
op otel rubber type* (&of 1). It could not be obtained by %he
.r=atLOA methods so far "ad. Th. miagre. re.) being

ciarked at by the s~thorw consists of too a a The first ...
to
Cf 2) -Lolded not mar
then
15% of -4prodlt
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.
.
*"am" Pat at. (R. 3croap d::.r 1;%in wa.tin
th
.
.Ai
tiom 1. still aj..ja4 ... far., the hors det.mi..d
: Th
Cc" 1/4 tL
t Is" .ad Itia" of i-bat". 610I.ti.4 with ethyl.".
p
in the Ir or these
(- 51-77! 9 at*. 1 5 145.
C;5 Cl. 5 a AICIP 2 ho~' h Yt ,, 2.3
4?%. Th. reaction is very sensitive to tomp*ratars
S , .01
(-Iy 1/3 of he lkylate yield at 35 ). The cataly.t "a be
Q444.5 to ttl so without r*dAclad %a* 4z"mtity Of alkylat: or
of23-dLS! byal-butans. Stbjl*ne has to be added d~rxad th
46010 Proose., its partial proseare ~% not *.aee4 0.5 - 0.7
On, or otboralse the 2.3-dinethyl-ba%ano content in the alkzlato
Martames rapidly. The addition of 1-~% C 21~" 'a""Mz- the
.1hyl.4"aft -R*r-
a da I pro, r f 100 - 200 :~:t.%ardtd to
.dt houlan. ad I. ccelareted by radta.1 da,mor.. :t
as"Sed oat by the sathars in -he presence Of C 2R5CI Cfair th.
first SUmm) in a special, ocotxm*~Ij vorhing plant. The &I.
0late 7iold (ccmpmt*d for atcylene) reached 17 -;a*% d-r
.mom oaadl%lomm (45on. 2co at.. reaction tin: ant a
go I ratio lsobutan* ethylene . 10 , 1. J.itimt!r~ - A%sity
4
2V
Card 2/4 ).2. 2-Dinothyl-bat". (52-35% of the alkyl~t.) ves, the
main pr Juall 2.3-dinothyl.butan* wao,~%*d to S-la% of the
alkq 1, %. Th* preparation of 2 3-dla:tbYI-bQtdl:n6
3-dinAthyl-butaut proo **do I' Z hY_1;3lt":Ltb
2
.0 .1two Ugww~ya) 4r t 0.
th ror"tica of %wo olqftn* I ) %a% ranot 1.4 thyl.... ..a
2) 2,3-diaoShyl-butom-1. b) D*hydzs-1oA of th
the duct. This r,,:flion has i&ot'bb---
,,t,:nd go
ow ., p- far h. r r.4c. a.patent (&of 5)). Th.
.t.or. .,::t,
'. ted the first stage t1sorcuiftly an 68 A-
ohrgal"-potgol" catalyst. Th* specifications 'or its pr-I.-
Iton cars pr vi d.4 by X. S. W.-hxtz (d.t....d) IM 11 ~"R
."titate of Organic Cheats-ry AS X.
h Is'
Ighost activity at 55ao. -no c4t4l7 B** *:a It . IA
the -he
a., 'a,
hjtzac&rh -67~1. Th.
Ine,,got %h . ::a. ad st o has ~t yet be,.,
a or
aromatisatLoo disgra
t on. Several mono-, bL-, And tricyalla hydr r on* wl.~,
is
:2"Ibod structars vor:wro.1,o:A.;z ll,:ib,:,
4, dlegres of the r-otL. %h .12
at .4 is, .1. 3 1-. there 1. d--4
"':a uu a.-Lad phenol
CorA 1/4 far tf I--'
a goooFfRi-ro -t,%**S - _,_ : !r-d Iy
tt yxmh *":d
7's-trz/F., ... present one, :r!oy* a:1. th".d at% ... a
mhow:rsL&htbbecoc` .".ful for Industry. In . J.P14
am 4kynt "is f r polzpbmzl syst- 1. -99-t-4. Nor .... r.
"t ftvorskls reaction to mentioned to the paper. There or. ii
reverences, 5 or which are 3o,iot.
AMMUTMM* Testoohno.3ibinkly fili.1 So 1". 31-11 CZ-t Bjbrl~ Ara.4h Of %no
SumuffiftDopertment of tbo 4c14-j of Sclancos. "_:)

S , ~
30), OV/71 -29-8-,-9/8 1
ctlZia:-ev3'-Jy, L., Shvartsbe=, S.
TITLL: Unsaturated Hydrocarbons. VII. Synthesis of n-Methyl-diphenyl
iit 10.~ ICAL: Zhurnal ohshchf-y 'r-.hi;.Ai, 1959, Vol L`9, .11r d, rP ',".~9-226-43 i)
A35TRACT: The authors were interested in the arTlication catalyti--
al'%)w-L.L.~aLIOL r,.U~;LiOU carriua out in trie Va,,E;rs -j!
1 and 2 for the synthesis of the polyphenyl systems, the carbons
cf the diphenyl-triphenyl series, and others. The attempt at
carrying out the cyclization of the 2-methyl-5-pheny'L-hexane-
diol-2,5 into the p-methyl-diphenyl was unsuccessful, since it
yielded mixtures (Refs 5,6,7). In the present paper, the follow-
~ng synthesis of n-methyl-diphenyl (I) by means c-f aromatiza-~:*.o:7-
6f compound (II) or its hydrogenation -z--~)dacts (ITI', and "I-~
according to the scheme was s-ugeested: t.-Le diol (I!) can be ob-,
tained, according to Grignard (Ref 8), from 3-inethylbutin-l-ol-3
and acetophenone, or according to the reaction of Favorakiy
(Ref 9), in smaller yield. The aromatizaticn of (II) probably
takes place via compound (V) by denydration. This aro,~atizaticn
Card 1/2 was carried oat .on the catalyst MgO(Cr 203 )A1203 (2:18:8o) at

,insaturated Hydrocarbons. VII. Synthesis of SOV/79-29-8-39/81
n-blethyl-diphenyl
380-5100, but the maximum yield was 11-13% only. In order to in-
crease it, the diol (II) was transformed, as previously, by
hydrogenation with 2 mnlaBof hydrogen into the glycols (III) and
(IV). Thus, the yields were 42 and 46.5~-, respectively, in the
aromatization of the glycol (III) at 4620 and of the glycol
(IV) at 55oo. The structure of the n-methyl-diphenyl was con-
firmed by oxidation with permangamte into the lk-phenyl benzoic
acid as well as by spectrum analysis, in accordance with the
constants available in publications. It was shown by catalytic
treatment of glycol (IV) on quartz, that the aromatization of
the glycols (II),I(III), and (IV) is of catalytic nature. Finally,
the authors expressed their gratitude to A. S. NakhmanoviQ"Or-
his assistance in taking the absorption spectra and to Yu. E.
Fayershteyn for carrying out a number of analyses. There are 2
figures, 1 table, and 16 references, 8 of which are Soviet.
ASSOCIATION: Institut khimii Vostochno-Sibirskogo filials. Akademii nauk SSSR
(Institute of Chemistry of the East-Siberian 3ranch of the Aca-
demy of Sciences, USSR)
SUBMITTEDi May 29, 1958
Card 2/2

- , ' -" , I ~ : , -, .
VT
SYRMERGI M. S., Cand Tech Sci - (diss) "Synthesis of certain
I polyphenyl hydrocarbons starting with acetylene compounus," Irkutsks
1960, 8 pp, 150 cop. (Institute of Chemistry of Eastern Siberian Affiliate,
Siberian Department, AS USSR) (KL., "-60, 1311)

VASILIYEV, Ye.K.; SHVARTSBERG, H.S.; KOTLYARMSKIY, I.L.
Roentgenometric constants of some aryl-substituted acetylene
glycols and their transformation products. Izv.Sib.otd.AN SSSR
no.2:111-113 160. (MIRA 13:6)
1. Vostochno-Sibiraldy filial Sibirskogo otdeleniya All SSSR.
(Glycols )

S/074/60/029/012/001/004
BO13/BO78
AUTHORS. Shvartsberg, M. S., Kotlyarevskiy, I. L.
TITLE: Methods of Synthesis of Polyphenyl Hydrocarbons
PERIODICAL: Uspekhi khimii, 1960, Vol. 29, No. 12, pp. 1439 - 1473
TEXT: This is a review of papers on the syntheses of polyphenyl hydro-
carbons. The preparation of hydrocarbons with a ramified polycyclic chain
is not covered here. About individual questions of the synthesis of poly-
phenyls there are several reviews in technical literature (Refs.2-5). The
existing methods of preparation of polyphenyl hydrocarbons may be divided
into five groups. The first group includes methods of lengthening the poly-
phenyl chain. To this group belongt 1) pyrolysis (Refs.6-59); 2) prepara-
tion of polyphenyls from aromatic amines: a) reaction according to
Gomberg (Refs.60-68); b) synthesis over nitroso acyl amines (Refs. 1,
69-81); c) direct synthesis from diazo salts (Refs.82-91); d) other methods
(Refs.92-100). 3) Arylation with peroxides of aromatic acids (Table,
Refs.62,74, 76, 7L 92, 101-117). 4) Preparation of polyphenyls out of
aryl halidest a) reduction on the palladium catalyst (Refs. 118-120);
Pard 1/3

Methods of Synthesis of Polyphenyl Hydro- S/074/60/029/012/001/004
carbons B013/B078
b) reaction according to Ullmann (Refs 31, 81, 121-145); c) reaction
according to WUrtz-Fittig (Refs,130, 141, 142, 146-163); d) magnesium-
organic synthesis (Refs.124, ,64-184); e) preparation from other metallo-
organic compounds (Refs.180-208), 5) Desulfurization and "deselenization"
(Refs.209...211). To the second group belong syntheses without alteration of
the cyclic carbon skeleton of the molecule (dehydrogenation) (Refs.1, 73,
76, 77, 80, 167~ 134, 187, 212-267). The third group encompasses syntheses
without alteration of the aromatic carbon skeleton of the molecule. To
this group belong: 1) Alkylation (Refs-254 -268 -282); 2) synthesis over
aliphatic-aromatic ketones (Refs.64, 271. 281, 283-298); 3) magnesium-
organic synthesis from halogen polyphenyls (Refs.76. 222, 254, 257, 281,
291-293, 299-302); 4) removal of functional groups (Refs.81, 135, 137,
98-100, 218, 303-314), 5) synthesis from heterocycles (Refs-313, 315-317).
To the fourth group belong syntheses in which the cyclic carbon skeleton
of the molecule is isomerized and split (Refs.218, 'zIB-321). To the fifth
group belong syntheses in which individual links of the polyphenyl chain
are formed (dehydrocyclization) (Refs.322-329), K. Andrianov, F. Kvitner,
V, Titova, A. A, Vvedenskiy, A, V, Frost, Ya, I, Mikhaylenko,
0. M. Zasypkina, Ye- A. Vdovtsova. 1. P Tsukervanik, S, V~ Zavgorodniy,
Card 2/3

Methods of Synthesis of Polyphenyl Hydro- 5/074/60/029/012/001/004
carbons BOIIA/BO78
and V. I. Sidellnikova are mentioned. There are 1 table and 329 refer-
ences: 63 Soviet.
ASSOCIATION: Institut khimii Vostochno-Sibirskogo filiala Sibirskogo
otdeleniya AN SSSR (Institute of Chemistry of the East
Siberian Branch of the Siberian Department of the AS USSR)
Card 3/3

TITLE: X. of' 4,141 '-D-Irreth-1-
y 1 1) i I t I I a 1. e. r) e
'PERIODICAL: Zhut,rijl ob,,lichey kh~mlL, P)60, Vo.L ."0, M-
1) p ,,I _~)0-4,,io (ussit)
ABSTRACT: T I ie Li i i t I lo r -s s yn t he .,, L -. c (I !I -d 11 me t I iy 1 b Lp he rl y I
aml (11) "Carn 2..!,5-tr1rnethy1--5(41-
(111) and 2-meth,,,,1-2-
(IV) by the
Collowing scheme wrlil-ch also gjves the synthetic routes
I U
f'ov the irltermediate-o
1.113 11,C c1l, C113
+
oil Oil

I I'c
cIt,
C' I I."
off
-Ni
Oil of[ If
MI WI CH.,
(V I I I
21,

Url3atucal~ed Hydro,~acbons . X
SOV/1' 71 9 -"~0-2 - 17/1
Aromatization of both tetrahydrofurans was performed
in a flow system at 550-560 0 over MgO(Cr,.o3)A1 20-5 (at
a ratio 2: 18:t30 for I and 2:( 5,L" !3, and 18):(95, 90,
85, and 80) for II; the best results were obtained
with 8% Cr,)O3), The tetraftydrofurans (20 or 40%
solution In benzene) were mixed with the catalyst and
fed into the System at 0.75-80 (for Ir) and 0.55-72
kg/liter catalyst , hr (for II). Yield of 4,41-di-
methylbiphenyl (I) was 47.4-48.2%, mp 120.5-1210;
0
yield of 2-phenylnaphthalene (11) was 28-31%, mp 94-97
Some of the constants found for the intermediate
products are: 2-mett,-yl-5-(4'-metl,-ylp',,ienyl)~iexyne-3-
-diol-21,5 (V , mp 94-15-950; 2,2,5-trimethyl-5-(41-
methylphenyfltetrahydrofuran (III), bp 88-890 (3 MM),
dj~ 20 0.9465, nD20 1.4996; the byproduct of hydrogenation,
_I "IL
" 'r- .0 -5 mm)~ d20 20 1.c;242;
Card 3 /4 VII. b p 12 2) 0.9596: n
k D

Unsat~-j--ate---,' -;iYdi-oc~17bons . X
SO"'lly 9 - -0-
1-(l '-~iydroxycyclotiexyl )--~'-phenylbutyne-l-o-1-3 (VI)y
rro 124-1241 .50; hydration product of (VI), the
saturated glycol (VIII), mp i2'T-12'T.50; ---methyl-2-
-ph.eny" -5-sPirocyclohexylte'vraiiydrofuran (-LV), bp 122-12"50
1 .5 rpm), d~. 2 0i.oo96"nD01'5255; 2-pheny1naphtha-
quinone-1,41'(Ix), which is an oxidation (with chromic
anhydride in acetic acid) product of (1-1),mp 109-110-50-
There are 2 figures; and 8 references, 3 Soviet, I
German, I S',-iiss, I U.K.., 2 U.S. The 3 U.K. and U.S.
references are: R. A. Friedel, M. Orchin, Ultraviolet
Spectra of Aromatic Compounds, N. Y. (1951); M. C.
Kloetzel, J. Am. Chem. Soc., 62-, 3405 194o ; D. H.
Hey, S. E. Lawton, J. Chem. Soc. , 3'j'4 H940~.
ASSOCIATION: Institute of Chemistry, East-Slberlan Branch of the
Academy of Sciences, USSR (Inst1tut khlmll Vostochno-
Sibirskogo filiala otdeleniya Akadem'L'- nauk SSSR)
SUBMITTED: February 15, 1959 Card 4/4"

sov/(~)' - --: j-2 - !
M. S., Tvotsenko, Z. F.
TITLF unsm't it t'a tel i Hk i 1-o". [-bOnz, XI. S-mthesls of u-Terpheni'a
PE1110DICAL.- ZhIIL'r;'IiI 01~.5110h-.'ily kh[ITIU, VOI '~O, NIC 2,
Wssli)
A B ST R A C' P par,zi-Tevphenyl (1) wa s by aromatizat-Ion of
dehyilv,,Atlon pr-oducts of .-),')-bil)iier-iythe.~atiecliol-2,5
(11). The follow1mr, s c h (3 rne LIlustvates the synthesis
t-oute

i."';I jf(*

Olt Q:i U h!

cil, c'f;'

~C

Card 1/_-I 62)

Unsaturated Hydrocarbons. ZT
A
St
cai
-17867
SOV/79 -30-2 - 1
The (III) Is obtained as
,5-bl~)hen~
a M,_Xtuve at' t,,~io lsonlcl~s (with mp 162-1650 (IIIa) and
12-2-123' (111b)), wi-tlch, upon hydrogenation (over-
;kcletal Ni) give ,~orvesporiAng, dLoIs (IIa and Hb).
Dehytivati-an of' bot-h Corms, gtves 1-dentical re-gults,
a mixture a~ V and IV. Avorwitization ot' the latter
prodi_zcts conduc,ted In the Clow system desevibed
ealviler (Ko 'I,- lyarev-,;k !L,,,,, 1. L... Shvartsberg, M. S.,
Zhui,. abohchey k1him., over
M~ ~O (Cr ~O )A L ,~Q feed,ing tile reactants

S/079/60/030/009/004/015
BOO1/BO64
AUTHORS: Kotlyarevskiy, I. L., Shvartsberg, M. S.
TITLE: Unsaturated Hydrocarbons. XII. Synthesis of 4-Methyl-p-
terphenyl and 4,4"-Dimethyl-p-terphenyl
PERIODICAL: Zhurnal obshchey khimii, 1960, Vol. 30, No. 9,
pp. 2912-2916
synthesis
TEXT: The of the substituted terphenyls by dehydrogenation and
cyclization. (Ref. 1) previously carried out by the authors could proceed
by two methods, i.e., by aromatization of the glycolsland their dehydra-
tion products containing either one diphenyl substituent or two phenyl
substituents. 4-methyl-p-terphenyl (I) was synthesized by the first
method, 4,4"-dimethyl-p-terphenyl (II) by the second. Condensation of
p-acetyl diphenyl with dimethyl ethinyl carbinol according to Iotsich
gave rise to 2-methyl-5-p-diphenylyl hexine-3-diol-2,5 (III), which, by
hydrogenation in methanol with a skeleton nickel catalyst passes over
into the respective hexane compound (IV). The latter is smoothly convert-
ed into 2,2,5-trimethyl-5-p-diphenylyl tetrahydrofuran (V) by the action
Card 1/3

Unsaturated Hydrocarbons. XII. Synthesis S/079/60/030/009/004/015
of 4-Methyl-p-terphenyl and 4,4"-Dimethyl-p- BOO1/Bo64
terphenyl
of HC1 in benzene. The aromatization of glycol (IV) and tetrahydrofuran
(V) (Refs. 1, 2) results in 4-methyl-p-terphenyl (1) in a yield of 50%.
2,5-di-p-tolyl hexine-3-diol-2,5 (VI) was obtained according to Favorskiy
from acetylene and p-methyl acetophenone (Ref. 3). Glycol (VI) was hydro-
genated to the hexane compound without separation of the isomers, and
furthermore passed over into the mixture of 2,5-di-p-tolyl hexadiene-2,4
(IX) and 2,5-dimethyl-2,5-di-p-tolyltetrahydrofuran (VIII) by dehydration.
The structure of the diene (IX) was confirmed by ozonization under the
formation of methyl acetophenone. The hydrogenation of glycol (VI) pro-
ceeds slowly in the last stage and results in the mixture of saturated
glycol (VII) and ethylene glycol after absorption of 70-90% of computed
hydrogen. In this case also 2,5-dimethyl-2,5-di-p-tolyl-e-dihydrofuran
(X) was separated in dehydration apart from the diene (IX) and the tetra-
hydrofuran derivatives (VIII). The glycol (VII) and its products of de-
hydration (VIII) and (IX) were aromatized to the compound (II) (yield:
30-35%) with the catalyst MgO/C 20 /Al2 0 Figs. 1 and 2 show the ultra-
violet spectra of the compounds mLtion~d*. There are 2 figures and
7 referenoes: 4 Soviet and 3 US.
Card 2/3

Unsaturated Hydrocarbons. XII. Synthesis S/079/60/030/009/004/015
of 4-?Aethyl-p-terphenyl and 4,4"-Dimethyl-p- BOOl/BO64
terphenyl
ASSOCIATION: Institut khimii Vostochno-Sibirskogo filiala Sibirskogo
otdeleniya Akademii nauk SSSE
(Chemical Institute of the East Siberian Branch of the
Siberian Department of the Academy of Sciences USSR)
SUBMITTED: June 11, 1959
Card 3/3

SHVARTSBERG, M.S.; VASILIYEV, Te. K.; KOTLYAREVSKIY,, LL.
Unsaturated hydrocarbons. Part 13: Coursi and,limits of
anplicability of the dehydrocyclization reaction in the syn-
ftimis of polypbenyls. Zhur. ob. khim. 31 no-4:1278-1284
Ap (MIRA 14:4)
lo Inatitut kbimli Vostochnosibirskogo filiala Sibir-skogo
otdeleniya.Ai~demii nauk SSSR.
(Aromitization) (Polyphenyle)

33273
S/00-2/62/000/001/014/015
AUTHORS: Kotljarevskiy, I. L., Shvartsberg, M. S., and Kruglov, B. G.
TITLE; Synthesis and oxidative polycondensation of 4,4'-di-ethynyl
biphenyl
PERIODICAL: Akademiya nauk 35SR. Izvestiya. Otdeleniye khimicheskikh
nauk, no. 1, 1962, 184 - 185
TEXT:- N hydrogenation of p-diacetyl biphenyl on skeleton nickel catalyst
at 50 60 C, the authors obtained in almost quantitative yield:
CH CH-C 0
3 ~)- a -CHCH3 (11), melting point 161.5 - 162.5 C. This compound
6H 6H
was dissolved in dioxane, and dehydrated by an Al 20 3 catalyst at 3300C.
The resultant, unpurified 4,41-divinyl biphenyl, dissolved in Ccl , was
brominated: CH 2BrCHBr-n/N - a-CHBrCH 2Br, This tetrabromide had a melting
W
point of 204-204.5 0C (under decomposition), the yield referred to II was
14 - 16~o'. The tetrabromide was dehydrobrominated by KOH to 4,4'-diethinyl
biphenyl (Yield 50 - 55%), melting point 163 - 1640-C. This compound may
Card 1/3

33273
S/062/6?/000/001/014/015
Synthesis and oxidative ... B101/B110
be polycondensed in pyridine with CuCl as a catalyst, or in aqueous-alco-
holic solution with CuCl-NH 4Cl. The following structure is assumed for
the unsoluble, yellow or orange-colored oligomer:
H [C~CCT_,~- Q -C~C ] H.HC1. The oligomer does not explode when heated, and
W n
is poorly inflammable. The infrared spectra taken at Academician I. V.
Obreimov's laboratory in the INEOS showed the bands for 1,4-substituted
aromatic rings and for acetylene hydrogen. The presence of carbonyl
groups due to partial hydration of the triple bond of the end group is
also possible, There are 4 references: 3 Soviet-bloc and I non-Soviet-
bloc. The reference to the English-language publication reads as follows:
A. S. Hay, J. Organ. Chem., 25, 1275 (1960).
ASSOCIATION: Institut nefte- i uglekhimicheskogo sinteza Sibirskogo
otdeleniyu Akademii nauk SSSR (Institute of Petro- and Coal-
chemic~tl Synthesis of the Siberian Department of the Academy
of Sciences USSR)
Card 2/3

h f b
AD Xr. 980-14 31 JkY
POLYMER WITH TETRAACETYLENE GROUPS IN THE BACKBONE JUSSR)
Shvartsberj[,-K-5,-,,_I. L. Kotlyarevskiy, and V. N. Andriyevskiy. IN:
Akademiya nauk SSSR. Izvestiya. Otdeleniye khimicheakikh nauk, no. 3,
Mar 1963, 575-576. S/062/63/000/003/018/018
A highly unsaturated polymer (1) whose conjugated chain consists of alter-
nating aromatic and tetraacetylene groups was prepared for the first time at
.the Institute of Chemical Kinetics and Combustion, Siberian Department Of
C&A 2/3

AID Nr. 980-14 31 MV
POLYMER VIM TETHAACE71IMM GROUPS (Cont'd] 8/062/63/000/003/018/028
the Academy of Sciences USSR. The-polymer of'-4---buta*di-y'n'yIp*~enyI other (U)
had the following probable structure:
7%
HC2.-C-C-=C-//'i %\-O- -CxC-CMC-
CIWC-C~C41 \~-O- (FVC~C4-CX=C- C'-WC-CMC---
\Axld
C=-C-C=--CH
Monomer II, which was synthesized in a2076 yield from 4-tkcetoacetylphenyl
ether, is stable only in dilute solutions, discolors in air, and decomposes sit
Card 2/3

SHVARTSBERG, 4.S.; KOTLYAREVSKIY, I.L. -, VUFSHCHAGINA, A.A.
Highly unsaturated polym6rs. Report No.6:
PolY-(1,30-triethinylbenzens). Izv. AN SSSR Ser.khim. no.10g
1836--2838 0 163. (MIM 17-3)
1. Institut khImicheskoy kinetiki I gorenlya Sibirskogo otdeleniya
AN SSSR.

KOTLYAREVSKIY, I.L.; SHVARTSBERG, M.S.; ANDRIYEVSKIY, V.N.; KRUGLOV, B.G.
Highly unsaturated polymers. Report No.7: Linear polynuclear
diethinylarenes and their oxidative polycondensation. Izv.
:1
z- AN SSSR. Ser. khim. no.11:2032-2036 9 163. (MIRA 17.1)
1. Institut khimicheskoy kinetiki i goreniya Sibirskogo otdeleniya
AN SSSR.

L 642994$ EWT(m)/EPF(c)/MA_(d)/WP(J)/T W/W
ACCESSION NR: AP5020990 UR/0195/65/006/004/0766/0766
a V
541.7
if
AUTHOR: Boldyrev,, V. V Shmadt, 1. V,-; Pislmenko, V. 1. Shvarteberi, M..'S
Kotlyarevskiy, 1. L.; Andriyevskiy, V. N.; Nomarov V. F
TITLE: Effect of additions of organic compounds with c9njugate bonds on the rate
'Zi ,
of thermal decomposition f solid substances
SOURCE: Kinetika I kataliz, v. 6. no. 4,.1965, 766
TOPIC TAGS thermal decompositior4 solid kinetics,. conjugate bond 9 stem,
y
silver compound, topochemistry
ABSTRACT: It has been observed that certain or anic compounds with a ysfe,
of conjugate multiple bonds exert an,effect on the rate of the rmai'de compositiono
7W
Tests were made of the effect of heterophas aidditions (5% on the weight of oxa
e
of conjugate alpha, omega- diarylpolyenes (I)- (IV) on the' rate of thermal decom-a
position of silver oxalate at 133C. A figure is given which shows a plot of the
gree of conversion against time. Results show that additions of the above
Card 1/ 2

I
KOTL'YARFW,Ui~ 1.L.-, SIVIARTSDFRG, M.S., VOLGINA, G.-I.; VASILEVSKlY, S.F.
of s~etylenlc derivatives of diphenyl crxide an-I
Izv. AN SSSR. Ser. khlm. no.9-1704-1706 165.
(M--rRA 18:9)
Ira t! tut kh irr-4 cheskoy kinetiki i goreniya AN SSSR.

ism
L 24312-66 EWT(m)/EWP(j)/T RM
ACC NRt Ap6oO9795 SOURCE CODE: UR/0062A6/000/002/0302/0308
,AUTHOR: Kotlyarevskiy, Is L.; Shverts-berg, M, S*; Vasilevokiy, S, F
AndriyevsRly-, V. 14,
ORG: Institute of Chemical Kinetics and Combu iberian ~6
Depar cbeskoy kinetiki i
gorenlya SIBIralcogo otcleienlys. Akade ii nauk)
TITLE: Highly unsaturated polymers Report 13- Polynuclear
noncondensed dietbyny1srenes
SOURCE: AN SSSR. Izvestlya, Seriya kbimicbeskayes no. 29 1966s
302-308
TOPIC TAGS: polymer, polynuclear hydrocarbon, aromatic hydrocarbon,
alkyne, condensation reaction, polymerization,.pol-yeondensation,,
solubility
ABSTRACT: Reactions were run to confirm that tbe-Introduction of metbyl
groups or of an oxygen bridge In the p-polypbenylenelsegment of a
dietbynylarene molecule increases its solubility, thus permitting the.
syntbesis-.of diace~ylenes~oontalning a gres.ter number of rings. The
ii-ere s~ntbesized- 11 24-dietbynyl- 23
following compounds 0 -
dimetbylbipbenyl, 11, 44-dietbyny1-lAj 23, 37-t ~3- tetrametbyl-p-
Card 1/2 UDC: 547-362+541.61

2~312-66
ACC NR: AP6009795
,~tbyny1-4'-(p-etbynylpbo epY ry Polymers of
quadripbenyl, and poxy)bipb 1
these compounds were O'bt6iiied by oxidativ- -lyconde'nsatiorl In alcobol-
e p
x
pyridine witb a polycuprous cbloride complee so catalyst* Condensation
could not be effected in aqueous-alcobol or aqueous-acetone solutionsl,
The polymers obtained were partially soluble In benzene. Orig. art*
bas: 1 figure*
SUB CODE: 07/ SUBM DATE: o9oct63/ ORIG REF: 003/ OTH REF; 006
Card 2/2

L 23278-66 T.TP(C)
ACC NRi-AP6q,12532 SOURCE CODE: UR/0062166/0-00/003/0527/0533. Y.2-
j 1W
AUTHORi Shvartsberg, H. S.; Kotlyarevskiyj I. L.; Andriyevskiy, Ve Nes
ORG: Institute of Chemical Kinetics and Combustion, Sibe-rian Depsrt-
ment of the Academy of Sciences SSSR (Institut khimicheskoy kLnetikL
L gorenLya SLbLrskogo otdeleniya AkademLL nauk SSSR)
TITLE: Highly unsaturated polymers. Communication 14. Polylble-
(butadiynyl)areneel
SOURCEt AN SSSR. Izvestiya. Seriya khimichaskaya. no. 3, 1966,
527-533
TOPIC TAGSt organic semiconductor, semiconducting polymer, poly-
acetylene, polyphenylene
ABSTRAM New poly(bis(butadiynyl)arene) oligomere h&ve been synthe-
sized as part of a systematic Investigation of the effect of structure-
on the electrical propertied. of conjugated polymers, 7~0 aligoners
were prepared as follovs:
Caid 1/ 4 UDCi 542.952+547*362

L 2327'~-66
ACC NRi AP6012532
0 --CHCOCHXO-// \\-O-e )-COCffsCOCHP-;!
Oy)
M
C-C-CH-o'
(XI)
11 (CmC'7CMC-'O, 0-//--;k,
(XVI)
(V)
07,
cocit,-
OCH
-Cmc-c-mcH
07/'C
(XVII)
-quou.. ~,,-rHcocHCO-e -CH.CH.--,'
-~OMWCH#-:
(VI)
Card 2 4

ACC NRi AP6012532
lic=-G-cac-//
(XIII)
(XVIII)
Cifxb -cocIl,-4CllICOctljco- -COCIICOCH#
(Vill) (VIIF
IICMC- 0-//--%-cmc-cwctI
Cr.C-
(XIV)
r
(Xlx)
Gil Gil~
CHS
c ArCcocll,~*Cllfcoctlfco
OX) M
Gil c1l,
-OHC=-G-C=-G C=C-CMCH-
(XV)
Gil Gil$
it (c=-C-C=Zb 6:~ r.G-C=r-).H
(XX)

L-03272-66
ACC NR: AP6012
Preparation of tetraketones I, II, III, VII and X and of tetraacet-
y1enes XI4 XII, XIII, XIV, and XV is described in the source. The
tetraacetylenes%were subjected to oxidative polycondensation in
pyridine in the remence of cuprous chloride. Oligomers XVI-XX were
brown to black powders. EPR data are given. [Electrical propertie 10
are not given in this article), Orig. art. hass I table. ism]
SUB CODE% 07/ SUBH DATEs 04Nov63/ ORIG REFt 005/ OTH REF: 003
ATD PRESS I
Card 4/ 4

L 4'~72~)-6f; FN-i ( m ) A, T/T R
AC-C-Wr, -AP6024413 . - - - -( A --- SOURCE CODE t _-UR/Oo20/6-6/169/001/pi I lh-.113~
AUTHORt Dulovs A. A.; Slinkin, A. A.; Rubinshteyn, A. M.; KWyarevskiy, I. Leo,
Shyartsbarg, M. S-;-Anoriyev . Yiiiina, A, S.; Sherginal 5. L
_Am. 14. D. Zelinskiy, Academy of Sciencest SSSR
URGt Institute of Or anic Chemistr-y
(Institut organicheskoy khimii Akademii nauk SSSR); Institute of Chemical Kinetics and
Combustions_;4berian Branch,,A adeny of S �R-lInstitut khimichaskoy kinetiki
q______�giqnces, SS
i gor'eniji Sibir-skogo ot-delenlya. Akademii n~S~�_R)___
TIM: IrIfluence of disturbance of conjugatio Ion the properties of semiconducting
SOURCEs AN SSSR, Dokladyp v. 169p no. 1, 19669 111-113
TOFIC TAG31 semiconducting polymer, conjugated polymer, semiconductor conductivity
ABSTRACD It has been frequently reported in the literature that the disturbance of
conjugation in organic semiconductors as a result of either noncoplanarity of aromatic
irings or introduction of aliphatic, oxygen, or sulfur bridge@ into the conjugated
Ichain 3.owers the electric characteristics. In the present papert the intensity of the
iinfluence of these different types of conjugation disturbances was compared in a se-'
ries of polymers of a single class, the polyarylone~olyac2lLlene8'lyhose electrical
conductivity or and ESR spectra were meavir-ed- tion I various groups die-
a The Introthic 0
turbing the conjugation into the conjugated chain was found to hinder the processes of
112

L 45725-66
I- ACC NRt AFW4413
I
current transfer. The relative effectiveness or this hindering Influence of different
groups may change with the flexibility of the moleculesp which affects the int*rmoloc-
ular interactions. In particularp the biphenylene groupingg which sharply decreasev
the electric properties of "linear" structures, does not affect the proportion of poly
mers consisting of more flexible oxygen-containing moleculeg. It to notable that
bridge groups do not appreciably lower the semiconducting pr"rties, The paper was
presented by Academician Kazanskiy, B. A.,, 230ot65. Orig. art. hael I table.
SUB CODES 07/ SUBM DATES 23Jul65/ ORIG REFS 014/ OTH REFS 003
COM 2/2

ACC NR
, AP60251101 souRcE oom: uR/oo62/66/000/007/1272/1275;
AUTHOR: Shvartsberj, M. S.; Andriyevskiy, V. N.; Kotlyarevskiy, I. L.
...7 ... woo-ft--w
ORG: Institute of Chemical Kinetics and Combustion, Siberian Department, Acadeqr
of Sciences)SSSR (Institut khimicheskoy kinetiki i goreniya Sibirskogo otdcleniya
Akademii nauk SSSR)
TITLE: Synthesis of some di- and tetraacetylenic amines
SOURCE: AN SSSR. Izv. Ser khim, no. T, 1966, 12T2-12T5
TOPIC TAGS: diacetyleniq amine, alkyl arylamino diacetylene, tetraace-t~ylenic amine
acetylene compound, amino, chemical synthesis
ABSTRACT:
!The physiologically active acetylenic amines are usually obtained in low-
lyields by the time-consuming Mannich reaction. It was found that in the
2presence of CuZC12 at 40-80'C, depending on the diamine present, aryl-
;diacetylenes'react with paraform and secondary amin'es to form l-N#N-
dilalkylamino-5-aryl-2,4-pentadiynes:

Ai-6o25401
Table 1. I-N,N-dialkylamino-5-aryl-2,4-pentadiynes
Y'
.
d -d Hydroch1v 64e
R W R" "
,
I ~Ts jrormul V(c
CA

c
mp.

.- rmula
la Mp. c
It 4C.H.- C.11- 74.3 6.86 CIA11"N 6.61 2242 175,5-111.5 11.02 C,111, NjO, 12,72 164-165 14.62- C..11"ON 14.21
11 -(Cit.).- 71.0 6.25 6.lt,,N 6.2? 2243 Its-fig 12,21 Cm .IfwH4OP 12.39 2)2-214
* 13,59 ~;Ojlwam 13.65
Wecomo
.)

H -mcmocitcit- 55.3 6.48 Cj&IIuNO 6.12 2245 - 176,6-160 Ii.se c.,rIrjNO 13.53
CM.- C611,- Coils- 80,1 5.72 COIJOH 6.53 2230 361.5-139 IJ,42 4,11_440, 31.56 220-7z; moy C"H*QN 12,24-
1 . (decom~.)
-(cIfl,_ U.4 3.40 C'SUMN 5.28 2236 tff,S-146 11.44 Cw"wNcOs 11.33 225-22? 74 c"ll'an 11,73
(cloomp.)
51,7 3.30 Ic- IIUN
01 5J4 2236
. (decomp.)

op 73.5--74*C (petroleum other)
sp 67-68.S*C (petroleum other)
Card

C NR. AP6025
Under the same conditions, condensation of p,p'-bis(butadiynyI)diphenyl
-ogide'with paraform and diethylamine gave the tetraacetylenic amines V
;(mp 52-52.5%) and VI (mp 150-152'C):
HCHO. IIK(Clifah
JIC=C-C=C-C:V)-O-(// -G=C-C;aCH
(I V)
(C*II&)sNCHsC=C--C=G-//~\ -0-f CmC-C-=CCII.N(C,11,)*
M
(ClHo)mNCIIsC=-C-CaCe-o~)-O-,\/~ --CmG-C=C-G= OZ 0-
-(VI)
-04-N-Cuce-Cm., CCHqN (CeH4
Orig. art. has: 1 table. (W.A. 50; CBE No. 10)
GTH REF: 001/
07i'S~BM DA!d: 22Dec65/- ORIG ]REP: 004
Card 4/4

SHMITSIMG, 11.
1 .1 . ..... .... .o
Ensuring reliability of radio apparatus In the Arctic.
Mor. flot 19 no-5:21-23 My '59. (MIRA 12:7)
l.Starshiy, inzhener nauchno-issladovatellskoge otdols, TSentrallnoge
b,,,ruro nauchno-tokhnichasko7 informataii Goskomitets, po radioelaktronike.
(Arctic regions-Radio-Apparatus and supplies)

SHVARTSBERG, S., inzh.; NOVIKOV, Ye., inzh.; SKVARCHFVSKIY, I.; KORNEV, M.;
I A., inzh.
Exchange of experience. Avt.transp. 42 no.1:48-50 Ja 164.
(IERA 17:2)

SHV.a%B=. Ta.;KOZITBUTA, X.F.;URW=H,V.X.iUY?SZVA, S.M.
Treatuent of scleroms, with streptom7cin, F torinolars, Mosina
14 no.2:65-67 ftr4pr 1952, "a-1-1-o(CLA 22:1)
1. Honored Vorker In Science, Professor for Shvartaborg; *ssistact for
Nositakaya; Departmental PkWelcian for Derkach; Semlor4l 1aborator7 WoRker
for Zaytseva. 2. Of the Clinic for Diseases of the Bar. Throat. and goes
(Director -- Honored Worker in Science Prof& Ya. A. Shvartsbarg). Kiev
Medical Institute.

SHVARTSMG, Ta, A., KOZITSKAYA, K.N.
__ __ ------
Complex therapy of seleroma, Yost. orinolar, NOskva
15 no.6!44-47 %v.-Dej- 1953. (CUM 25:5)
1. Professor for Shvartsberg. 2. Of the Clinib for
Diseases of the lbx, Throat. and None (Read -Prof. T&. A.
Skyartaborg), Kiev Medical Notituto and the Division of
the ftnicipal. Clinical Hospital of First Aid.

,5 H V- tq 4k T-5 -D rz e (~) YA fl ,
SHYARTSBZRG, Ta.; MNTSUZOV, B.
Activities report of the Kiev branch of the Ukrainian 5ociety of
Otorhinolaryagologisto for the year 1953. Test. oto-rin. 3y no.4:
90-92 JI-Ag 154. (KLRA 7:8)
(UKRAIMI--OTORHINOLARTNGOLOGY--SOCIWIM)
(OTORHINOLARTNGOIODGT--SOC IST INS--UMAUM)

SHARTSBERG, Ya.A.p prof. zaaluzhennyy deyatel' nauki USSR, Kiev.
-111! , ~" .1,
Otolaryagology in the Ukraine. Vest. oto-ria. 16 no-3:3-6
MY-Je '54. (XWA 7:7)
1. Predsedatell Ukrainskogo nauchnogo obshchestva oto-1mingologav.
(OTORHINOLARYNGOLOGY,
*in Russia)

SHVARTSBERG, Ya.A., prof*, zasluzhennyy deyntell nauki USSR.
Nikolai Marianovich Volkovich; an the centennial of his birth,
Vest.ato-rin. 20 uo,6:110--112 N-D 158 (MIRA 11:12)
(VOLKOVICH, NIKOLAI MARXIANOVICH, 1858-1928)

deyatel' naul:!; "'RITSKIY, L.A.P
deyatell naul-i- S':'IARTSBT2RG, Ya.A., prof.
ce--mate'll na- :i; K
dclktor mod. nauk; TYTAIRI, G.H., o*610.1aringo-log.
Pvc)Veosor Leon Antonovich Lurkovskii; 1903 or, his 60th birthday.
uoh., r~o.-- i -,or. bol. 24 no.2:92-93 II-Ir-Ap 164
WIRA 18:1)

I'ladMOL'.11 IIV7~~'. Jv:~

CHOCHIA, K.N., SHVARTSBMG, Ye.M., STOLYAR. Ya.
Blood transfusion In control of postirradiation leakopenja
[with summary in Inglish]. Nederad,* 3 no.5:84-90 S-0 158
(KIRA 11:12)
1, Is ?Sentrallnogo nauchno-looledovatelookogo rentgonoradtologl-
cheskogo Instituta Ministerstys, zdravookhraneniyaw
(IBUKDCYTE, COUNT.
leukopenta after x-ray ther., prev. by blood
transfusion (Rue))
(BLOOD TRANSFUSION,
In lankopenia after x-ray ther. (Rua))
(RADIOTHMWY. compl.'
leukopnia. prev. by blood transfusion (Rua))

SHVARTSBERG, Ye.H. (Leningrad)
Rtidintion therapy of bladder tumors. Urologiia 23 no.3:32-38
MY-Je 158 (MIRA 11:6)
1e Iz radiokhirurgicheskogo otdelenlys, (zov. - dots. I.N. Chochia)
TSentrnllnogo nauchno-issledovntel'skogo rentgeno-radiologichaskogo
inatitutR (dir. - prof. M.N. Pobedinskiy).
(BLADDMI. nOOPlARMS
surg, & radiother. (Rus))
(RADIOTHERAPY, in vnrious din.
cancer of bladder (Run))

CHOCHYA, K.N.; SHVARTSBERG, Ye.M.
Study of the function of the thyroad gland with the aid of radio-
active iodine during radiotherapyfor cancer of the larynx. Med.
rad. 5 no.8sl4-18 160. (MIPA 13:12)
(IARM-CANCER) (THYROID GIAND)
(IODINF--ISOTOPES)

BUEBYEVA, L.I.; GORSHKOVA, Z.S.; GUBER, L.U.; ILIE4, A.G.; KOZHUKHOV)
VOKO; PISHCHIKOVj D.P.; TYKACIIINSKIY, I.D.; SHVARTSBEYN, Ye.A.;
TASLITSKAYA,, M.G., -rwd.; BORISOV, B.L., tekhn. red. -
[Manufacture of glass insulators) Proizvodstvo elektroizoliato-
rov iz stekla. Moskva, Gos. nauchno-isel. in-t steklap 1960,
73 P* (MMA l5sl).
1. Nachallnik laboratoriy v/v izolyatoro; Vsesoyuznogo elektro-
tekhnicheskogo institute, im. Lenina'(for Kozhukhov). 2. Nachall-
nik laboratoriy steklovaremiya Gosudarstvennogo nauchno-insledo-
vatel'skogo instituta stekla (for Tykachinskiy)
(Electric insulators and in;ulation)

SHVARTSBUD, S.I. (Moskva)
Training of programmers in secondary polytechnic schools
of general education. Mat. v. shkole no.2:19-29 Mr-Ap 161.
(MIRA 3-4:4)
(Programming (Electronic computers))

'"LIMA f~l i Li:_t.3(~nt; M&7,0R;1MK, PSYUK, S.K.; GHAYKA, K.L.;
ant'hyaluz,-.r"L,,.sa an-I critanecus reactions to
in r, cri.-Is and luVa.-, erythen-atoms. Vest. derm. i ven.
38 nc.7.-!?-2l J-1 164. (MIRA 1814)
!. Fifedra darmatu"Icgit (zav. dotsant N.I.Tumasheva) Vinnitskogo
ir.3ttuta.

SHVARTS13URD;,I" kandidat takhnicheakikh nauk; SLEPNXR. B.N.. inzhener.
Surface finish of hydraulic machinery parts and application of
the All-Union State Standard.2789-45. Trudy VIGH no-13.-88-134
'51. (NIBA 1018)
(Ketals--Pinishing)

D.-Illing an(,' Poring
Coordinate broaching of the rin-s of high pressure worm pumps. Vest. mash., 12, ',.*,o. 2, 1952
1
Monthl List of husElan Accessions, Library of Congress, Cctober 19,12. Unclassified.

USSR/Miscellaneous Machine Tools
Card
Authors : Shvartsburd, B. L
Title : Profile milling of sharp-pointed contour cutters
Periodical Stan i instr., 3, 18 22, Mar 1954
Abstract I The design and construction of'new profile milling machine for mach-
ining profiled sharp-pointed cutters is discussed. The main factors
taken into account in the design were the profiles and the pi-eeision
of milled parts. A detailed analysis of the design, with diagrams
and illustrations of the machine is given.
Institution
Submitted

SHVARTSBUIW, B.I., kandidat tekhnichoskikh nauk.
~:,. - ~w~ ~v-
Machining of axial turbine and pumping-machinery blades. Trudy
VIGN no.17:25-62 '54. (K6RA 9:3)
(Hydraulic turbines--Blades) (Machinery autowAtic)

SHVARTSBURD, B.I., kandidat tekhnichaskikh nauk.
. -
Highly productive technology for the manufacture of screw pump
casings. Trudy VION no.'17:63-73 154. (NLRA 9:3)
(Pumping machinery) (MachirAi--ghop practice)

SHVARTSBURD, B.I., kandidat takhaichookikh nauk.
."
N.sw methoa_~f shaped-and wIll-edge for screw-pump screw willing.
Trudy VIGH no.17:13&155 '54. (NLRA 9:3)
(Killing machines)

SHYARTSBURG', B.I.-
Profile grinding of shaped, sharp-pointed cutters. Stan.i instr.
25 no.3:18-22 Mr 154. (KLRA 7:5)
(Outting tools)

BELBTSKIY, D.G., kandidat tekhniches~ikh itauk: KORSAEDV, V.S., kandidat
.4_ kaa-
takhatcheskikh &auk, dotsent, retabasent;-SRTART
didat tekhmicheakikh nauk. retsenzent: TOS M SANSIIY. N.N., insho-
&or, redaktor; POPUTA, S.K., tokhnicheakiy rodaktor.
[Technology of pump cometructioal Tokhmologila anaosestr9oalla.
Moskva, Gem.sauchne-tokhis. isd-vo washinestroit. lit-ry. 1956.511 p
(Pumping machinery) (NLRA 9:61

JS
t5
h
r A
An- lei ,j t .11
J4
83 It .81
At

SHVARTSIVRD. B.I., kand.tekhn.nauk
----
Technological processes for cutting screw-shaped impellers for
screw pumps. Trudy VNIINMASH no.1:61-87 '59. (MIRA 13:5)
(Screw cutting)

25(
SOV/28-59-5-2/30
AUTHOR! Shvartsburd, B.-I.L Candidate of Technical Sciences
TITLE: The Use of Universal Assembled Fittingstj
PERIODICAL: Standartizatsiya, 1959, Nr 5, pp 6-9 (USSR)
ABSTRACT: The author stresses the increasing use in the machine
Fittinis
building industry of the Universal Assembled
(USP Universalno-Sbornyye Prisposobleniya). About
80 plants now have their own fittings of this kind,
comprising 3,600 to 60,000 units. Such is the
arrangement made by the Mosgorsovnarkhoz. These
fittings can be used many times in differently assimb-
led units, and if the unit is not wanted for over
3 months, they are usually dismantled (and not scrapped).
The use ofthese fittings is organized in the following
4 ways: 1) They are centralized at each of the plants
using them 2).They are centralized at the industrial
area or to" (as in Moscow) 3) They are centralized
according to the specialities, so that the fittings
Card 112 are issued on loan to the factories for a temporary

SOV/28-59-5-2/30
The Use of Universal Assemled Fittings
specific work,order only. 4) They are centralized
separately or in completely assembled units. The
works which manufacture these fittings have their
own problems to solve, such as 1) to establish normal,
standardized sizes of these fittings, and 2) their
uniform quality of material, out of which they are
made (usually steel mark 18KhGT). The largest and
smallest sizes are the least required, presenting
another problem for the manufacturers and for the
centralized stores. There are 4 diagrams and 1 table.
Card 212

S t3- --Is"kavicb; SHVARTSBURD, Semen Isaakovich;
UMANSKIT, G.S., red.; HAKHOVA, N.N., tekhn. red.
[Problem in matheizatics for schools specializing In machine
building]Zadachi po matematike dlia shkol a mashinostroitallnol
spetsializatsioi; posobie dlia uchitalei II-XI klassov. Moskva,,
Uchpedgiz, 1962. 93 P. (MIRA 16:1)
(Mathematics-ProblemB,, exercises, ate.)

STIVARTSBnD, E.V.
Structural equations of a system of four partial differential
equations of the first order. Uch. zap. MGPI no. 243:192-199
T65 (Itm lg..l)

25M
SOV/135-59-5 201211
AUTHOR: Shvartsbu-rd, G.D., Director, Berezk,'n, P.N-,. Deputy Chairman
TITLE7, A Conference of Readers of "Svarochnoye proizvodstvoll
PER I OD ICAL! 5varochnoye pro"~-ivodst%ro, 1-959, Nr 5, P 46 (USSR)
ABSTRACT; The engineer,.ng and technical active members among the welders
of Chelyabinsk wanted a readers' conference, so the local off-ice
of the welding section of ChelyabNTO of MASHPROM, together with
the municipal scientific and technical library of T9BT1 of the
Sovnarkhoz, arranged one. Seventy-seven representatives Gf
local planis and institutes took part. V.S. Chernyak, the
scientific editor of this journal, gave a talk on the work and
tasks o_,: the journal. Everyone agreed that it was a good
journal but had a few defects; better coverage of concrei~-_ pro-
duction experience, especially on ccmplex automation and mech-
anization, more diszussions and book reviews were needed. It
was considered necessary to suggest publishing a mass produc-
tion and technical. Journal "Svarshchik" for the masses. Every-
one hoped "Svarochnoye proizvodstvo" would carry on the good
Card 1/2 work in the 7-year plan.

m
SOV/135-59-5-20/21
A Conference of Readers of "Svarochnoye prolzvodstvo"
ASSOCIATION: TsNTB of the Chelyabinsk sovnarkhoz (Shvartsburd);
'Welding Section of ChelyabNTOMASHPROM (Berezkin).
Card 2/2
11

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, 21 2. WIST11 111V
fractions Mill. for lint4runi is not hivniogrn"Mrs, anti 11jr
,l the re,in wr atil cwtildvIrly si-,I-
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coneuvOke. A. 1. Kocan and L. R. Shvitruburg.
00 lCjWmj*wl 6. 215-17OW10-Some -00

0 diffesent quarrim tested for acid res;iiiance wrem found
0 suitable for the comtruction of 110SOO towefs. Afore
00 reliable remits were obtalmd by teod"s by the method

410 of Kheaka (C. A. 25, 4M) than by the method of hoiling
a rxiwd. sample for I hir. in coned. Hj9O4 and writthing
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lorernove bin ftom "a. and then filtered. Fivessil.s4the
~4n. was mixed with 3 ad. of 119% 11,14)o wood the inial.
0 at, Noun with Its to remove the Ot. The polarograms
it- not greatly affrl-jed loy the large struls. P(Al andothes,
:
its till- .4n. TIw bright of she U.6,srs W:1'
ft.,"Mi till K~ figh'sq% IWNIICI lltws Vs. F"Itawn .41"flif the
its costs, .1 istts. ¬ the jitatwr f.t.-ti the hil.., jah.lig
'
ttidinstic was taken as the height of the wave. Ilu
the
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cu~. lilt 1-se r"sults. The av. crr,-r 1,v .1 5d, sits. wa..
00 0' And Ito A- Its it was .1 3%. 'Witrial lissfull'i detim can tv
of '3 itiadc in 2 ht. Vitt- aso.-thimi -wit lw t"A fm Ictg is tic,
00 WcormoreMo. It has no exceptional advantiLit" over
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it is -lopst* Il. Z. Ksoinich
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�brArtsbuto, and 1. A. '.nfefuun. Zarxi-
"
0 0 J%. W-44tjQ4q).--I)etn.o( Sn in ,rrA is best
sba:m L~K
done o4twimetric-Ally with
wif t1l) III dil. Ms. W. '1711. --f Cl, i. kept fe"In Interf"-
at by a,kits. cif cOrk- ot,ul, I In.-al"AW -.1.1 1. Ilse's I.-
11
o. u- Sta to the [AvAlirnt stair mi-I A filtir --os is t1--,1 I-
keel. tile IV's So Inewapti'le it, -'uhl~ foc
"A',ciluctry. Against mand.u.1 .4m. 1,11C .1W .1,1tv, 1. ..1.
-its RIA AdJk. und IWO11. thaq cmi Iw u-1 m"n,
00 a 4 xrpa. W Sit wben rAlbet snutIl aints. Arr dralt with 0 Ite 40 0

00 "I). oRrvilwi f,,r
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;00
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SEV.'iRTSFU-D, L. Y-;~&
USSIR/C I., evli.~ f,r -- Per -.-I J i i I] Y-r 150
VIP I-lication of Beni:iAne to Analy5is of 1~.oz,-~.otlunlgStates," 7. A. Nazarenkc, L. Ye.
Shv.-..rtsburd, 1 F
"Z,-vod Lab" Vol XVI, No 3
FA 159T4
Describes experiments which demonstrate possibility of precipitating phosphotungstic
acid with benzidine. Latter may be used successfully in case when amount of phosphotungsten
complex in solution or in solid salt must be determined.
IA 159T4

SAIMATOV, I.P., Zasluzhermyy vrach RSFSR; MARTS, Yu.E.
Billroth I operation in stomach cancer. Xhirurgi-,a no.8:62-65
Ag 162. (MIM 15:5)
1. 1z Vologodskoy oblastnoy bollnitsy (glavnyy vrach V.P. fwban)
i Vologodskogo oblastnogo onkologicheskogo dispansera (gla-vnvy
vrach N.A. Mataruyev).
(STOMACH-CANCER) (STOMACH-SURGERY)

SHVARTS, Yu. E. (Vologda)
Surgical treatment of pheochromocytoma. Klin. med. no.8:71-73
,6:L. (MIRA 15:4)
1. Iz 'Vologodskogo oblastnogo onkologicheskogo dispansera (glavnyy
vrach N. A. Mataruyev, zaveduyushchiy khirurgicheskim otdoleniyem
Yu. E. Shvarts)
(ADRENAL GLANDS-TUMORS)

ShVCRT-"OVF O,S,, kand.t~i,:in.maiA; *IPVARTI~')) Y.:.F.,, nzll,
Performance of rails hurd~~ne--J in oil. - 9
no.8:41 165. (MIRA 18:8)

SW/Aiqrlj, Z. "'. -3,1'anova, K. -.; 3assav--;!,Y~~ ~. ,
I 1 1- m.
Th5 State Optical Institute: (GOI) Lerdngrad
IIDaP.,ind,jnc,5 of light dams of the eye on the size, of oclour sources of livht"
Doklady Akademii Nauk , Vol 53, mo 6, lq!~-,

"I
, JfVA13T!-',, ':,. M.
"Dependence of Sharpness of Depth Perception on the Contrast Difference of the
Objects vith the Background:"
Problemy Fiziologicheskiy Optiki, No. 8, 1953 PP 336-340
abs
W-31.098, 2~6 Nov 54

137-58-5-9364
Tra ns la tion from: Referativnyy zhurnal, Metallurgiya, 1958, Nr 5, p 80 (USSR)
A UTHORS: Mayants, A.D., Orlova, S.I., Barotitskayi, F.I., Shvarts,
Z. M.
TITLED Employment of Various Oxidation Agents in the Production of
Zinc Sulfate From Solutions Resulting From Leaching of Pow-
ders and Sublimates of Zinc Production (Polucheniye tsinkovogo
kuporosa iz rastvo~ov ot vyshchelachivaniya pyley i vozgonov
tsinkovogo proizvodstva s primeneniyem razlichnykh okisliteley)
PERIODICAL: Sb. nauchn. tr. Gos. n. -i. in-t tsvetnykh met. , 1957, Nr
13, pp 134-146
ABSTRACT: Leaching of dusts and sublimates of zinc production was car-
ried out under laboratory conditions. After being previously de-
contaminated of As, the solution underwent crystallization of
ZnS04- Pyrolusite, atmospheric 0?, and gaseous Cl? served to
oxidize the admixtures contained in the solution after leaching.
It was found that standard ZnS04 can not be obtained by employ-
ing pyrolusite. Most rational method is the employment of atmo-
spheric oxygen in which case practically all of the Zn is obtained
Ca rd 1/12 in the form of standard technical sulfate which is suitable for any

137-58-5-9364
Employment of Various Oxidation (cont. )
application. If advanced purification of the solution is difficult, gaseous C12
may be utilized as an additional oxidizing agent in place of the atmospheric
02.
L.P.
1. Zinc, s-,_11Tate---Produc t ion 2. Arsenic--Separation 3. Zinc jo-lutions--Oxidatiop
4. 1)xygen--Applications 5. Chlorine--Applications
Ca rd 212

1, - ne nr c i., imn',-s o p c r
S.
2(
Len -in.,-
so: u--irC5(), Jime 53, (Iet-"z3:-, 5,

VALYUSKIY. N.M., podpolkovnik meditainakoysluzhby, kandidat meditainsklkh
nauk; SHYARTS, Z.3h., podpolkovnik moditain5koy aluzhbv, kandidat
mad K'URATOVA, P.A.
Using some physical therapy methods in chronic gastritis. Toen.-sed,
zhur. no.3:31-34 Mr 156. (KLVA 9:9)
(STONACH-MUSIS) (PHYSIGAL THERAPY)

I
OLCiLOOV, yeV., SHVAhT6, ZS~; PLTAOVA, GJ.; GH-I~ATUU, L.F.; MISE.,~&O,
M
T. I.
Sixtieth birthday of Professor Aleksan&- Prokhorov4ih larfenov.
Vop. kur., fizioter, i lech. fiz. kullt, 26 no.6:163-56 ",-D 161.
(PAMNOVY ALEF.~ANDR PROKMOVIGH, 190:-) 15:1)

38238 SHVARTSAPELI,
-
Kombikormovyy zavod v sovkho-ze. (Tipovoy proyekt). Yqas. Wustriya
SSSR, 1949, No 6. a. 66-7o