SCIENTIFIC ABSTRACT YASHUNSKIY, R.G. - YASHVILI, G.M.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001962220015-3
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: September 1, 2001
• Sequence Number: 15
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

L01793-66 DIT(d)/W(l) JjP(c)
ACCESSION NR: AP502i624 UR/0286/65/000/013/0105/0105
621.9-529
%tA
1AUTHOR: YashunskiX, R. G.; Pinson* T. B.
!TITIE., Prograpmed-control system. Cl4ss k9, No. 172615
3 1,4%1
ISOURCE: Byulleten' izobreteniy.i tovarnykh znakov, no. 13, 1965, 105
1TOPIC TAGS: programmed control, sequence switch
ABSTRACT: An Author Certificate has been issued for a programmed-control uystem,
consisting of a switching device and counter, which controls the operation of elec-
tric motors such as those arranged on the rotating parts of rotor lines (see Fig. I
of the Enclosure). The switching device is in the form of an insulating ring
-1equipped with segmented current-conducting inserts equal in number to the number of
,motors being controlled, thus assuring the necessary motor svitch-on sequence. This
devine simplifies the control system and increases its reliability. Orig. art. hast
I figure. [WHI
'ASSOCIATIOi: none
[C*crd_,

ENCL40SURE: 01
. 0
. 1: - -- - - - - --- - , -

AUTHOR: Yashunskiy, R.G. and Arkhipov, N.A. 113-58-6-13/16
TITLE: A New Automaton for Controllable Reversal Current in Galvanic
Baths (Novyy avtomat dlya reguliruyemogo reversirovaniya toka
v gallvanicheskikh vannakh)
PERIODICAL: Avtomobillnaya promyshlennost', 1958, Nr 6, PP 37-39 (USSR)
ABSTRACT: The NIITAvtoprom elaborated a new process of high-luster copper
plating in cyanic electrolytes. Research showed that the best
results are obtained by the controllable reversal current. The
./do it is to switch the current of the excitation
best way tq
winding,_of a generator with the help of electronic tubes -
thiratr"ons. By.the scheme of reversal current elaborated by
14
A.S T ge, two independent windings were placed on the poles
generators, one of which served to pass the 110-volt current
,A"'30911
in one direction and the second - in opposite direction.
X
Calculations showed that it was impossible to fix two 110-volt
windings on the generator of the AND-1500/750 and AND-5000/2500
aggregates. In this connection, new schemes of reversal current
with one excitation winding were fed by a 110-115 volt current
for AND-5000/2500 and AND-1000/500 aggregates. (Table 1) The
rectification of the-,current which fee :ds the excitation winding
Card 1/3 of the generators is made by two pairs of thiratrons. For

1 13-5e-6-1;11/16
,A New Automaton for Controllable Reversal Current in Galvanic Baths
AND-9000/2500 and AND-1000/50C type aggregates, the TRI-15/15
and the TR1-5/2 type thiratrons are used respectively. Each
pair is connected with the independent winding of the trans-
former. The cathodes of each pair are connected with the
opposite ends of the excitation windings of the generators
through the regulating rheostats and accordingly the middle
points of the anode windings of the~transformer are also con-
nected with the opposite ends. Thus, by the dual ignition
of the pair on the left, the current passes through the wind-
ings in one direction, and by switching on the pair on the
right, it passes through in the opposite direction. At the
same time the direction of the magnetic flux of the generator
and the current direction in its armature and in the bath are
also changed. The rheostats of excitation (lPB and 2PB) permit
the regulation of the current in the excitation winding and,
consequently, the density of the current in the direct and re-
versed directions. The alternate connection of the left and
right pair of thiratrons is regulated by an electronic time-
relay, mounted on a 6118C tube, by alternate feeding on its cir-
Card 2/3 cuit of the positive or negative potential in relation to the

11 A, -5,8-6-1
A New Automaton for Controllable Reversal Current in Galvanic Baths
cathodes. The feeding of the time relay and the circuits of
the thiratrons is made from the circuit of alternate current,
with 380 or 220 volts through the transformer 1T, which has
as a part of its initial winding the winding of anode voltage,
the winding of feeding the tube of the time relay and two
windings for feeding the circuits of the thiratrons. The
technical characteristics of the transformer are given. The
aggregates are built by the Yaroslavskiy elektromekhanicheskiy
zavod (The Yaroslavl' Electromechanical Plant). The description
and working principle of automaton are given.
There is 1 diagram, 2 tables, 2 photos, 1 figure and I Soviet
reference.
ASSOCIATION: NITTAvtoprom
Card 3/3 1. Galvanizing--Solutions 2. Electrical current--Control systems
--Ope,ration

YASHUNS p--LEVINA, I. L
Device for automatic -regulation of current density in electro-
lytic baths. AVt. prom. 29 no.0-35-37 Ap 163.
(MIRA 1626)
1. Nauchno-issledovateltakiy tekhnologicheakiy institut
avtamobi,11noy promyahlennosti.
Pleetxic controllers) - (Galvanizing)

YASHMSKIY R. G.- BOCHEVER., B. G.
__ , -,AV-.---,-- --V
Pickups for the recording of production output based on changea
in the current machine-tool motor circulit", Av4,,, prom. 28 no.61
3-5 Je '62. 4 (MIRA .1684)
1, Nauchno-issledovatellskiy institut av-tomobillnoy promysh-
lennosti.
(Electronic Instraments) (Production control)

SHUIMHKIN, Aj.; YASHUNSKIY, R.G.
Keeping records on and analysing the use of equipment in mass production.
Avt.trakt.prom. no-7:3-6 JI 153. (MLU 6:8)
1. Ministerstvo mashinostroyeniya.
(Machinery in industry) (Production control)

LASHCHIVE1,19 S.M..: SMGEYEV: S.I.I.1 ROZE212 G.M.; YASHUNSKIYp R.Go
Automatic line for mamLfacturing the air brake reservoir of thp.
ZIL-130 automobilia. A-rlv.prom. no.3.34-38 mr 161. (MIRA 14~,3)
1. Nauchno-isgledovateliskiy eksperimentallnyy institut avtotraktornogo
elektrooborudovar-tya i priborov~
(Automobiles- --Brakes) (ilosembly.-line methods)

YASHUIISKIY,, R.G.; BOCMVFR, B.Go,
Means of mechanization oi production control. Art. ptom. 27
no. 5:1-6 14y 'Al., 1 OMA 14: 5)
1, Nauchno,--~ssledovatol-kskiy tekhnologichookiy institut
avtomobillnoy promyshlenrosti.
(Automobile industry) (Automation)

TORCH1211SKAYA) O.L.; RAZUMOVSKIY, IT.O.; _pSjRjqK17).,,Y!G.; BAIAEUKRA), V.S.
USHAKOITA, V.F.
Excretion of radioactive cerium from the body under the influ-
ence of triethylonetetraaminehexaacetic and tetraothylonepento-
aminoheptoacetic acids. Radiobiologiia 3 no.2:270-275"63
(MIRA 17.'l)
P

KOST, A. 'if., TZR--7i,'T'Y3V, A. I%, YASHNONSKlY, V. G.
Azacyclo Compounds
Synthesis of 1-oxa-5-azacyclooctane. Vest. 'Mosk. un. 5, 11o. 6, 195o.
9. Monthl List of Russian Accessions, Library of Congress, November 1952 Uncl.

A. P, Terentlev, L. A. Yanovskays and V. G. Yashunskil "Sulphonation and sulphonic
acids of acidophobic compounds. XI. Application of the method of lixiviation
for the investigation of the products Of BUIDhonation of pyrrole." ( p. 510)
SO: Jourmal of GenenI Chemistry, Mfirmal Cbshehei Khimil), 1950, Vol. 20, Fo. 3.

KOST, A.H.; YASHMSKIY, V.Go
Aleksei Nlkolaevi6h Vyshnegradakii. Uspokhi Ehim. 21, 26o-4 152.
(CA 48 no.2:414 154) (XLRA 5:2)

K-"" Xt*
Koz T-' - A-. t t-;~ -f KS I IMS
Propionitri-les, Vvshnegrp-dskiy Reaction
Anomalous behavior of B - substituted propioritriles in the Vyshenegradakii reaction.
Dok3-. AN SSSR 83 no. 1, 1952
Monthly List of Russian Accessions, Library of Conp7ess) August 1952, Unclaarifled.

- - ---- -----
U S S R
'iriii6es' oifFthlodipro'plo'nic ac Id. N K6nr,
cdcv, and V. G. Vashun~ii Vesinik ~fojhrv'
Uriu. S. No. 3. Scr. Fiz.-Afal, i Eiterben. Auk No, 2.
111-14(1953).-Treating NuiS.911tO (I niole) with 2 mol
Ctl;:CIICZT dropwiie A 15-17', stirring 4 firs. at room
tcrap., gave an oily layer which, when extil, with Caffii.
washed, dried, and dktd, vielded 0,11'-dicyanodlethyl
MIM(le (1), needles, tn. 16", bt.,-s 163-0. nV IAM7. dt(
14270. Considerably luiver convemions were obtained ut
-ter rr~
as action ratin or higher t~!ntpi. Itefluxing 1 (0.143
l
--) 4 lirs. with If)() ml. coned. IICI yleMed 00% 0.0'-
mol.
-opionic The foll
Ahlodip. acid (11), in. 133.5* (from 1110).
'lowing derivs. of 11 were obtaineil by conventional methods:
di-M ester, b7 143*, nV 1.4648, d., 1,0051; di-Bu "ter
bit-it 1MV, ns? 1.1017, dx 1,0126; dianilide, m. 102.5*
(from r- t0lj); (11-1~-toluidide, m. 1938.5' (front M011).
-r
Gerard Auflcgc.
n2-

Anomalous reduction of 0 sul-Atitoted &rqVj &UL'kLt~;-
_
_ I
; is
N_R HAM k"r
VyshnrKrAdskil 41
I

.In
rl A,
LQ~
09S'); ;-I. CA~ 47, to
fri-M!, tqVropionitr0ri with ROU-Na'
method. J. J?f(t,. Phyr. 0nem. Soc. 12, 16
I&SO)l leads to smomalials results in that 3-alkoltypropyl-
aminei are formed, the alkoxy grnul) bting dtlived from lite!
'ROll used, The. reaction Pfucteds hy cicavage to Ctl,:.l
:CITC11, followed 1)), cyanor(hylallun of lite ROII and reduc-
thlo of the lesiliting altioxyllitrill" RefluXing 38.2 g.1
Cff;(CI4ClltTIr)s And 17.2 g, NaCZN its all. ELOR 10 lirs-i

Est. Ig.ive, ilftcr iteam distit, for the renitival of mirractcd dibro-!
I
it% ide, G Pinst looit rile, b, 1;W-VKJ*. ClI,i:CllCN (
2 V.
5 L
Ided slosyly to 2.1 g. Aft-Oil and 0.9 g. Na. then heatec I r'
54 on it -itearn bath, gave 7870 %fc0(JjjClljCV, b. 163-l';
lite RO an4h)g, 70.81,"D, and iEso-PrO analog, 71% ivere,
A
mistry . I I,Q
Prel)d, similarly; iso-AmOonalog,75.0%.1in 109,_10
121 g. PhOlf awl 1.6 g, Nix wais addvd over I hr. 67.9 g-'
Cjl,:CllcN at ]30-A, all(! lite, mixt.stirred 5hrs.. yieldine
'520,,', I'h0CI1,Cl[,CV. tit. Q*. Clj,:CflCN (39.8 g.)
addett c-,-~r 2 fits. to 46.5 g. (Cllpfl), and 1.8 gj
'25% NaOll %vith coolifig gave 47.S% IIOCIJIC1120cllr~
*
111-W, W.' 1.4443, d. 1.07(13, along with
clf2c:% Iii-s
.25 g, bij(cyanoeIhyIaIion)produrI, th 16G-71'. To IW
l
lip at 10* wis
added 79
5
M
IM
S
911
0 i
I-
.
,
m
5
.
n
2
g
;g.
CITI:CHCN and the raixt. stirred 4 fits. at romn temp.
Tc,22g.Nawa
3s

C!
added a 8.9 g. itimellmitrile in 330 nil. hot BuOll and t4
inixt. is at I r pidly(bati teml). 1.15*) until the Na bad
)
)
-Lr L~7

s"Olve, I ; t~r I I; I I; %I ml. trv a I I I I r I It an, 1 '11 e A it 10 V, I I I. R;kvr I I
Ii: BL dem'.. ill, Id.
I',. Chrm.
J. Rum PA
'
13f rea--flon oI 12., z. 1), with 39 P, N-I and
C30 lnI. BuOll xa.~v lfuf~ '~'7liC1I;Cll"vjl" -3"V
1),. Mf~-71)% w., go-op*
I f" O-X~T" ill(
-'Olid; pLe'ale. it). Ott'; ilz (Wiv- Iq 1(12- ,,*;
dectillip. Ily:)"), al") follimil ill 211 1)"*; YiOd Oil rvillictioll uf
ill BUM I. Rapid addo. of I-I'l g.
C113CN in 21W ml, bot FtOll ro '-'I) It. Ma br iul-~
ToMflate liwating fliall; tump. V~flk "") P.11y'. Eloclir!

J;lOCl1sCl1sCH,Nll( (71,)j~V111, lit. I 111 -17', I.A512. dv
().V)011), picratc, 111. 1-13'. To a bwIwl;5I')tI of 1.1 g. Na dilst
'in Nileflis wmaddrd aver 1.5 inin, 11.3 K. ill
(4) rifl. iso.-PrOll, thcyi 40 nil. i~,TrOl I to complete qoIn. of
the Na; the usual trealsojent gave 21 !',% iya-Prot"HIC112-
CHjNl1z, fill 74-5'. The 8uO ritialog 01)0'510)' obtained
similarly in SnOll, b,"RO-I '; isn-Am.0 a,,al"g, prelid. Atilt-,
latly in isa-AmOll, b,,,M-3', Ill'i 1.4312, il,.10.8517 (picrale.
lit. VA"). Retintlinn of 10.5 g. 'Mt:0C)IICII:CN in Buolf
with Na (without other solvent) gave 2.--R~-., nliOC[fjCllj-
Cl12iVlf3, n1so forilleA in 29.4,11; vield front HOCE1,C1112-
OCII:CI.IjCN in 1311011. Redilefion of PhOCIf2CII'C'-'
with Na in MePh in thie firewnre (if I'1011 gave 55.5%
.DO Cit.. CJ`fz CHINIf" bo "M -Q)'
in ISO fill. INAling'.1bl. I"Mil wal added Ill g, III; lbrimoal
tTC;Itmcnt Save 2.6 g. 1). and
C
~mc 1.5 R. ncillba'ic Inaterial; rctiliction kith Na in NIC1,11
in the pwicrice of i-,o-Plf)lf pi-s- i-,uT)()CIlICfl'ClIr'
INH:*, minctim) without solvew in j~o~ it 11011 gave.

O."144A
b'_ n 424n, is,
-
i
l
x]
ipi",tt" In' s
(Imm COWI: ij:o :it Tvilm lion in U11011
19ave '20" Toillai'm ;,I M"Ph in the
of i
n
A
oli
1A
-
s
ni
Nits, his (;f~-7'. Redimitm t;f CiC1l,CIICN' its IMellh sit
'
'
the presc-lice of B11011 y"we filic~ lj1iOClf'C
l1'Cfl:'V112. b~i
I7_8A"_a.nd 8:41"~ VfNli'.

-'symth-t-Eel vVilb ne CA ef Rv- I "X R-f 6'~ r
of L7 th-- V.
I AA, JL-Xq!j, and A. I,. I crmccv (777-
Zhur. Obs-"f
i
V

Ghemical Abst.
8
663h; 48.2WN-To 5.3 g. CY',-CTICN in

VOL 48 Mflu;fiis nal. alm rIOH was added nvrr ~'- min. 15 g
h
t
e mIxt. was dRd. with 100 nil. 1110 art, r c onipl,-tion of

Apr. 10, 1954 reaction. stc~-distd. Into 10% ITC]. -1 the Stell- -1

Organic Ohemistr7 tillate further treated will% stearn nil ev:,;), . yirldinFai-d
1
Which
with NaOlf u
de
Lt
3t
O
E
oclf
71
n
r
1-
. Ra"
t
1
.
!
,%
'(
CII,Nih, bw 194,4)'. To 'T g ~ INa in SO in 1. lint Me Ph - -
tidded in 0.5 11r. 11"I jr, Cil,:CIICN in 35o mi. mo-mim ~t
l4(),-rYO*, thca 200 mi. JEW after itnin. of the Na. and the
Prod ict ocam-dintd. ~~ above, yielding 63.1 cf,,
t,. 72-3', and 1.28 g. I'tNII, IICI 11-1
1,56'. A Similar rraCtion in DuOll gave 44-3',", flunolf,'
CIfICHiNfli, hn 78-9*, bj; 71-.'*; a ler,5cr propts"icm of
Cli,:CIICN gavt a M.A% ~icld. Similarly -w" formed
41.4% irO-AojOcHC11,C11,Ar11,, bil 781~80.0'
G. hi. Kn-,olar-ff
MEMOMMMMMMMEFROM
G;
Y

Ri 2 n' I-Ek M-5 f V-9 ~-i A 0-
Dissertation: "Addition ',-"C'act-Jon in the Alpha, Feta Unsaturated Vitriles S-ries."
Cand Cher- S'ci, Voscow Order of Lenin State U imeni Lomonosov, 5 Jun 154. Vecherr~yaya
f,',oskva, Voscow$ 27 1"--y 5-4.
SO: SUM 12'84, 26 Nov 19r4
-75- P, - -`?7-

-YA'sL- "'Y'
q A I
USSR/ Chemistry - Analysis
Card
Authors i Terentyev, At P., Butskus) Ps F., and Yashunskiy, V. G.
Oritle i Determination of acrylonitrile with the aid of the cyanothylation
reaction
Perlodical Zhur. Anal. Khim., 9, Ed. 3o 162 - 165, May-June 1954
Abstract i Inve*stiga tions conducted on the cyanotbylation of alpha-amino acid
derivatives led to the development of a now method for the determination
of acrylonitriles, based on the reaction of the latter with glycol.
The apparature employed in connection with this new analysis method
is described. The now analysis method makes it possible to determine
acrylonitrile in colored mixtures containing water and ethylenecyanohy-
drin with an accuracy of up tot 1%. Eleven references: 3-USSR, 6-USA,
2-English. Table; drawing.
Institution The M. V. Lomonosoy State University, Moscow
Submitted Jan. 13, 1954
Y~

7P.1:L
M
_USSR/Chemiotry Reduction processes
Card 1/1 Pub. 151 20/38
Authors I Terentyev, A. 11., and Yashun;3Ky. V. G,
Title Study of gamma-dinitrile reduction according to the Vishnegrad method
.Periodical Zhur. ob. khim. 24/2, 291-298, Feb 1954
Abstract It was found that the Vishnegrad method of reducing nitriles with Na in alco-
hol can be successfully utilized for the synthesis of certain hardly-access-
ible cvclic nitrous bases. The conditions and factors affectina the process
of cyclization, which is usually folloved by the formation of pivericline, vras
investigated during the reduction dinitrile with glutaric acid in alsohol.
Kxperiments shm;ed that dinitriles of alpha-methyl- and alpha-phen-i-Irrint-aric
4-
acids offer greater yields of cyclic products than non-substiuted dirlLtrile.
A method determinina the Direridine and ammonia contents in a rentametIrylone-
0
diaTrdne mixture is deucri6~. Fifteen references: 10-USSR; 3LGerman and 2-
USA (1885-1953). table's; graphs,
Institution
Submitted. 'July 131 1953

T vi " ~ - , , I ,
k.~: ~ WJI ~: , -~- U
I I . L Z ,
- , 1, 1- 11

61!thiAl 61 acryllo AtIds. with altriles. X= propm-.1:100, of
and -pipridine, ,.G. Ymhurislill
V.
:_imd Aj P. Tcrent'ev (ZA. cWth, Ithismi .1955. 25,: 2299-4303).
Dariv. 61 pyrrolldirb -and piptridine types -of - pharmat~ologl
interest- were obtained front - koxy ' ylarnines nnd s2malcbalal
J~ p
dibromidos. By conde=Ation of I : 4.1pbromabutana and I : 5-
d'b rn tano- with a 3-alkoxy ropylamint, krt,bascs wero
I ro opei~
F.
obtalued %vith pyriolidine and piperid no ringi, 3 Y~ro Inc
7-whea reacted with B,3-dibromodictltyl others gave ( -athoxy-
j propy))morpholiac. - The - loflo-Ning woro thus obtained -3-
i ethoxy-, 1-3'-isopropoxy~. 1-T-1,pitoxyw. 1-T-0obtitoxy- and 1-3-
isoptntyloxy-propylpyrrolldine, 1-J'-othoxypro yl~ and 1-3'~butoxy-
-piperidint, and 1-W-etboxyPropyknorp oline. A. L. D.
propyl
nY

./lyntherics witb
n X Krv-=cmpxmtivo re.
iLctmt7 Of acryloattr e wit
thw
hrL,-'
5 F
4
S.S. 1. 2K 1~
1
9), R,;zd, M. R.

. I .. . . i--: ; , ~ a r,* I , - " , ! 't ~ : ", - ~- ; . r~; ~ I I' - ~. - -
- I.-
- - - - . , - . : -'s
I

r
N KLAt. -,d- A ~7~rin he~
S'27-30kl'zl(AWh.ngNsh tranNLtiom C A, 50, i
XXVU ReaLion of d~' n s rithenal with ;ubstituted
acr7fcaltrilez ",' C. 1 e-,., -.
Va G NeLhIm 13 W'K.7i
17

I ~
AI I
-11h zcryhc tcid naril XXVU Dlene
;7 .7.- -_ 'f7_ - __'_ - -
%T~7: 777Mz,
iv
Le itf-r.
I- An Ar. Aml "'D4 1nsa tl"n oducts M it ins-
11 ,1 ", ed to S-ph,-nyi :5 11- onieltIvIencev I~Acx I ~ne-
hi: arid BN i~acung fumaric njtri!~ at I 10