SCIENTIFIC ABSTRACT KUPETSKIY, V. N. - KUPINSKAYA, G. V.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R000927610005-1
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: August 23, 2000
• Sequence Number: 5
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

KULTSKI 1L.--
~Tg-L-Y-
Recent developments in t1w old method of drift bottle release. Keteor.
i gidrole no-10:37 0 160* (MM 13:10)
(ocean.currents)

3/169/61/000/005/013/049
A005/A13O
AUTHOR: Kupet9kV,_Y,.11..__
TITLEt The effect of stable water openings on cyclone circulation
in the Antarctic
PERIODICALs Referativnyy zhurnal, Geofizika, no- 5, 58-59, abstract 5 B
479- (Inform. byul. Sov. antarkt. ekspeditBii, 1960, no. 21,
23-26)
TEM The author examines the role of stable water openings in in-
tensification and sharpening of cyclone activity in the Antarctic. These
water openings form irk winter under the action of centrifugal winds and
maintain their existence owing to the action of the inner heat of sea
water. In the majority of cases, the principal trajectories of winter
cyclones all terminate in regions where stable water openings are located.
Here the localization of depressions proceeds. In addition, it is mostly
in these regions that one observes the escape of cyclones towards the
continent, which is preceded by their regeneration incident to receiving
Card 1/2

3/169/61/000/005/013/049
The effect of stable water openings on A005/AI30
additional thermal energy. The fact that cyclones do not recede from the
continent as the ice edge recedes from the coast. but mostly head into
the continent, is explained by seasonal ohange-over of the thermobaric
field. Besides the main polar front running along the outer edge of sea
ices, a secondary front appears which runs along the stationary water
openings.
M. Sorochinskiy
(Abstractor's notet Complete translation.]
Card 2/2

-'J/l 6 9/6 2/000/01-2/05 6/0 9.5
"'220/0307
-)Ctc
3-1--u(,.nce of (IC(I-) ittlantic viater on some features-
of the .'xctic Climate
'C'forntivnily -,hurnal, Geofi.-,ika, -no. 12, 1962, 53,
abstract 123-3-51 (In collection: 1--iterialy :)o
no. 1, L.*1 1.961, 22-23)
T of curven of the riwz-m monthly temperature
varintion Zor 1.9:;0-1.931) -.c 90 polar stations from ~;:)itzberL;ci, to
.'~lasha showed that winter-, idth a "warr.,i corc," acre ol)servcr-l only at
15 stations, situited on tli~., Tayi.tyrokiy ileuinsula. Ecvc thc, -,~,Can
moLit1ily tcm,,,crativr,- S'n --'cbruary it; 'id,rher tha-a in januz,ry ~111(1
The source of w--rmth i,,; Oleo.) ~',tlaiitic water, which is to
the surj'z.,cc !3y proccs,-;c:-. of vertical vintcr circulation i-.1 -,tation-
ary polynia Of thc C'nster-'I part of thc 1:ara ~ca ~.md thc we-stern -.oart
of: the 1,a-,tev S'ea note: olynia are unfrozen patches
of watcr in the mid icc
st o 1 -7
'abstracter's noLe: ~omplcto tra-,,slation-7 C ard 1/1

YaGENOVO II.I.LK
Fif tieth work aradversary of
ships "Taymyrn and "Vaygach"
Okeanologiia I no.3:571-574
the nydrographic e peditiod of .he
in the Arctic Oce,i uqlc~-1015),-
161. (MIRA 16:11)

AULTSKUp-I.N. ,
Luminesconce of oca ice. Probl. Arkt. i Antarkt. no.9:105-106
161. (MIRA 15:1)
(Sea ice)
.,F- IlUminesconae)

KUPETSKIYt V.H., kand.geograficheskiki nauk
Not land but sea; new hypothecis on Sannikov Iand. Znan-oila 36 n,,.1:22-
23 Ja 161. (Geographical myths) (KIRA .14:3)

KUPETSKIY, V.N.p kand.geograf.nauk (Leningrad)
For-tion of ice on warm water. Priroda 50 no.7:125 ji 161.
QM 14:6)
(Chaun Bay-Ice on rivers, lakes, etc.)

KUPETSKIY, V.N.
Stationary spacea of open water among ice in the lvi'hite Sea.
I'mdy GOIN no.6408-92 161. (MW 3-4:8)
(White Soa--Soa ice)

HEASKIY, V.N.
I---- --
Marine landformB in th-3 Arctic. Izv. Vt3eij. geog. ob-va 93 rc.4:3C4-311
Jl - Ag 161. 1/.:7)
(Arctic voglona-4)ceanography)

KUPF,TSKII, V.N.
The stationary open water "Severnaya Voda" in Baffin Bay. Trudy
GOIN no.70:47-60 162. (MIRA 15:6)
(Baffin Bay--Sea ice)

KUPE'I'AlY, V.114.
Hintorl of the dircovel-f Of Sevarnftyi, Zemlya. Izv. VceEl.
geog~ ob-va 95 no.6528-530 N-D '63. (MIRA 1711)

I
, 1 4 -'TsKly,
Y E,,,'j EN OV 1. 1 . ; Ku:, L - --- - - -L. 11.
The Runnian polar explorer B.A,Villkitukli. Lot. Sov. 4:223-228 164-
(MIRA 18:3)

KUPETSKIY, V.N.
Warning effect of stationary polynyas in the Antarctic. Probl,
Arkt.i, Antarkt. no.15337-40 164. (MIRA 17:4)

I T 7 i 17 z -1 ! I ,.. .": ~ " - i i ; ~, -),; .
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( ' i - T , ~',
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SOV/1 12-59-1-9 37
Translation from: Referativnyy zhurnal. Elektrotekhnika, 1959, Nr 1, p 125 (USSR)
AUTHOR: Kupe and Sinegubkin, B. V.
_- -Y-1-
TITLE; Electrically-Driven Speedometer
PERIODICAL: Avtotrakt. elektrooborudovaniye, 1958, Nr 2, pp 33-38
ABSTRACT: Bibliographic entry.
Card I 11

KUPL-M. T inzh.; SINEGUHKIN, V.
Speedometers with electric drives. Avt. trangip. 36 no. 7:40-42
JI '58. (MIRA 11:8)
1. Nauchno-issladovateltakiy institut avtopriborov.
(Speed indicators)

MAU I PMK mnZrArCR Sorl-k-"n
&A~iosalYs Lately toy 3=. :nealtut onorSwUlL I o lost rA~V_ha1 kJ
il"Iesw tranepmoym -r-Utr, 3 J-rrIY -,11t-
tw Poese of 3 ) RIC%, 1360. 224 p. to: T-V.
Xrra4a GL:P ljooemo~t. 1,000 cvl,* pnn"4.
&,east: W.N. Tojrbartts Canulato ~f ;~I*acoo: T.r.
Aroolt, of A.F. C-11"t. of
$,I-; It- Y.. S-I'Y-: Toth: U.: T..Poeglloi.
F .,Me: !tLL. -1.1-tion e 1. for t--il-l --ro"
~ltft.1,ortrtal ..Vpzy Yt- for -- of tren.p.--Loo.
ccnmL-41 _- _1.1~.Ioo 1. tzs mird I* or .-k. r f
Power and El-trtcal Acclassy uf Szloa- Z^~Ttyskaju ~'Iml L-3 !..L
-Uh plobLosee -t.4 elm me l.tr1-1 -7PLY yet- I- -.roo Ioo.
XQW or %" arucl*e deal vim ei*rtft- avoorstors of 'L~triz po"r-4--r7li,
wyotesse r- rvl&2_~M poooonoIot cars, vita sss;*-!. ple,94 on me leaLCI Af a
wrochrocess grearstor eu . b%Llt.tn posor mcti:ior. )%-ter
eorned the -.lot of -41sti~ th. Lo".....O.-loo
Uasoolooss 3c-*soe& to a-r-osette rec-IIA-Lon cimults. on,t *-~* a7putotim If
oateabj. reortors 1. t-r.-r .-4b.t.t'-- R-r-- -P-7
-Ll.lso.
j"-jA_-_at Z.-stl4ation or - zl-tll~ xt-b1l.
,dp," Vim see A..C ~.oorvt.r it= 33
__toed
Taribl. Speed
A3w1t. T.T. Ame-seess ?-~A- of 4 $Yattroo~ K-hl- 97
lcd=tor ,..mt,r 69
Dsebi.--oota wlsou-4
I.&.Lt_ 1~rusor Vith "Vo St..-Toom
_ _r _ _
ft. 99
11seard1r4 the Tosewrat-o of Iooo,.mra '%Zi wt
cw 'lertoot - Itoo
SC!5~ of a TWmo4-A-t-* KNCM*~IC CIrt'stt L13
jqodV&lon.
L,2,,,, owed tJ-* *CL Solent- is i I
125
tq%lpt
tw_-1 Chreeterl.til. of . S.turabl-1-tor Xg-tl.
3.-C Von
U vloss C tZs Isor" -b*r of t7"v of roetiflers anot their
Uterstiantlosa of their estimated perfol,te voIU -o.artly torol,o
lallp Rosofter cc -Pwriewouts eoaso results wmdA be d"MI-It to utt ule in
The -,sm= W.Vosaa to 'u,-Id. U. P-blIes or
of soo anyllflir Into toc sts4is, LA ordar r1rot to do-
%arostsee me oeLLoost*4 pvr~_ of an Ideal rotift-, =1 wtoully
Is. tAk. tale' ac~oosot t.U off*-% or. recttrier rvolstan-. It Is szoo,x
th-16an't" ssqailll~ opereUtus at ae wtIre lood, the PrincLyles of do-
Isso seed tzes dwtersoloostics of unL""Li Pearzonce, sav t3s easev for
=VLLrjo~
_s mtLood UL~Zslioal ~ Lfi.r end ro, wpuTo o'Im
41. . . . go
to U W
seeplifters. *.g.' the ~t glan factor' the Power
fsoctow~. tw poeer Cede fuetor. out the rolune of stool and ~Vper. -t*
ainboo, -lLalsoo that Us ustA,oreal mrrvo obtalos,1 we raluable for de-
oarl- of snpuft.rs op.-%I=d Itzl --%I-
Los". Zd,tb" rw _rrying not A. qIalltatl- of - -VL'fl.r In
roogas% to cosiness peoveseters. Me Is tar are holpoLl to oeal,Ieting hoo
the load sne_trjsUc of an essplMor ~1;. affected b7 tructur%l casa4ve.
r-- refe-, LU gcw~.%.

KUPEYEV., Yu.; MIKHAYLOVA, Ye.; DELYAYEVA, V.; STWITSEVA, Yu.
Alternating current generator of the FAZ-652 motortruck. Avt.tranBp.
39 no.6:40-43 Jo 161, (KMA .14:7)
(MotortruckB-Electric equipment)
v

KMYEVP YU,A.
Criterla for the evaluation of automobile genorators. Avt.
prom. 29 no.1l127-29 N 163. (MIRA 161l2)
1. Nauchno-issledovatellskiy i eksperimentallnyy institut
avtomobillnogo elaktrooborudovaniya i priborov.

ro
4-1

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IHUXHRA. Tu.; KUMR, H.. redakto.?; EARTAKINA, M., tekhnicheoldy radaktor
(71ying bvdroplane models] Letainshchie modeli g1drosamoletov.
Moskva, lzd-va Donaaf, 1954. 65 P. (Hicrofilm] (KLRA 8:2)
(seaplanes) (Airplanes-Models)

KUMANIN, V.; RYVKIN, P.; KHODUVICII, Z.; SOKOLOV, Yu. ; KOSTENKO, I.:
KUMR, M.; VASII,'YEV, A.; POSTNIKOV, Yu. ; TAIIAXANUV, A.
More attention to plane modelina as a sport; letter to the editor.
lryl.rod. 5 no.12:16 D 154. KRA 7;1Z)
(Airplanes--Models)

LUCHMSKIY, losif Aleksondrovioh; YEFREMOVA, Ye.V., red.; KUPFRR,.N.A.. red,;
AhDRLWOV, B.I., taklm.red.
[Propellers for model airplanes) Vozdushnyo vinty dlia lataiuohchikh
modelei. Moskva, Izd-vo DOSAAF, 1958. 115 pe (MIRA 12:2)
(Propellers. Aerial-Models)

CIO
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L 42929-bb EWT (J),/EWT (1)/Di'r W/T- 2/ZJF Uh) -0c)
ACC NR: SWRCE CODZ: UTV00841661GW1C02/'
AP6017130 OW7 OC09
AUT4-.OR: 1. (Deputy chief designer)
ORG: None
TITLE: 'Nultipurpose helicopter of Ka-26 type
SOTUPCE: Grazhdanskaya twiatoiya, no. 2, 1966, 7-9
TOPIC TAGS: helicopter, helicopter engine, helicopter rotor Ka-8. helicopter, Ka-10 he]
MM-9 radio compass
copterA-26 helicopter, GSS-306 generate , f;ToI-17 ptu
ra-13 helicopter
A!!STPUCT: A new multipurpono, helicopter of Xa-26 type is described. It was desiened by
the Design Office headed by Chief Deoi&ner Nikolay Illich Xamov. The new helicopter
belongs to the Ka-series of coaxial-rotor helicopters ammong which Ka--5 of 35 hp (in 1946),
7-a-15 andka-18 types are equipped with a
K_--10, Ka-15 and Ka-18 are mentioned. Th9
KO-hp engine and are used for various transportttion purposes. The Ka-15 helicopter is
used mostly in agriculture for-glamical. spraying services. However, it can carry only
210 kg of chemical agents* Thimp the new Ka-26 helicopter was made of a heavier type
with a tare_- carrying 900 kg of chomioal products. It in equipped with two reciprocating
h of 325 hp and with two op -revolving rotors. Tho cruising speed is
on~;ine3, oac ponito
140 krl/hr reaching a maxirmim at 175 ko/hr. The flying range with 6 passengers if! 400 km
at a =ximum altitude of 3= m, The helicopter is designed for an overhaul period of
not 1e-93 than,1000 hr. Its spraying operating productivity is rated at 30 Whr. 7n0
Card 1/2

L 4292Q-66
ACC NRt JV6017130
crew cabin in designed for 2 members. She Ka-26 helicopter can also be used for trans,
portation of 6 passengers or 700 kg of goods. In this case, the helicopter is equipped
with a special cabin. With removed cabin or platform, it can lift and transport a
90D-ka load. The helicopter can be equipped with a 30-kw alternator for supplying
current to various farm implements. The helicopter is provided with a 4-wheel landing
goar. Ma arrangements of fusolago and cabins are described anx-1 some devices and auxil-
iary equipment aro nontionod. In conolusion, it in stroanod that by ohanging ito equip-
mant the Ka-26 helicopter can be easily adapted to various services such as transporta-
tion, ambulance, reconnaissance, etc. Orig. art. has: 3 photos and 2 &tetches showing
the general arrangement of the aircraft.
SUB CODE: Ol/ SUM DATE3 None
2/2 MLP

2)
Kupfer, S. L'.
R.-Aional :,'(Ahod of
Ceramic Feldoi~ar lluv~ Lla""Urjal
I
010.cniya nodr.-r-Mitudya kvitrturt
1-01'ri Byrtye)
t'l(.. -Jiartz Cojlt~nt ill
(11-tt'gion-allriyy i-~
._ 104
v levy .-.h,, atovw..
_DTCA!,: stcklo i pp
The dr--termination of tl.(; con on
accurdii.'L; to L;ectim'~I as by of tLe,
Com IC ,'-C C~.C::Acal unaiyois ml-ch TILC
autilor of 'thic article a uut!-~~:,I of -,,u~rtz deter-
mination on the ba3is of tizu Wal of Si(), 'by
L
tacans of a dia-Gram (soe fi~,ure). Tio mt~thod ou'~C.'.Octod is
based on tho fact t;:I'_0k. t I, u 'I'. , I ~ ei )--vo uO.-, d i n c e rami c
prodi'mction and t1le po-tion of' fuld.:p-tr Of V~'-,
consist of a mixtuve of :.i .~ :acid -.l:q;io-
clases. The conto.A of brund, Sil", in
Card 1/2 2,-)%r as well an in amwr.-":~ to 65"

Ratior;al Mothod of Dctorminin,,, thr-, ~iuartz contcur,!. if,
Ceramic Feldspar Raw Material
and dot:s not show deviatiojiL; of r..orc than + 1,,-j' in t!,c
feldopar raw materials uoizr~11.y usc--d in ceramics. In t!,e
.'.able tli,~ results of of t' - -u-ar'z
by r.-,eans of various methcAIr aro In this case
the deviations accordiiC~ to Mle graTlilcal -Ict"od
aro much leas i,
.njortant than in tl,.c o'U!.cr rcthod:-, of do.-
torminat.-on. In conclusion, the author says that the nt;w
method is more accluratc than ti-.e conversion r,,,:,,thrid of
chemical analysis. It may bc used fcr rappid entii-.1ation.
of tl.,.(,, quart,- content and thuc poosible a chu6-- cf
tho rart material quality in cf-,ca!-,.ic -!ork!;. TILQri2 i-,
Card 1112

ETIPFER. S.H - XAGIDOVICH, V.I.
Granitic rocks as raw materials for glass and ceramic
industriess 'Razved. I okh. nedr 25 no.12:1-6 D 159.
(MIR& 13:6)
1. Ural'skoye geoltrpravleniya (for Kupfer). 2. Ministerst-
vo geologii I okhrany nedr SSR (for ", dovich).
(Granite) (Glans manufacture) (Ceramic industries)

XUPAR, S.14.
Now deposit of feldspar as raw material for the ceramic and
glass industries. Stek. i ker. 18 no. 3;25-27 Mr 161.
(MIRA 14:5)
(Rezhik region-Feldspar)

KRAVCHENKO, A.Ya.; KUPFER, S.M.
Efficient formulas for determining the volumes of blocks in cal-
culating reserves by the method of cross sections. Hazved. i
okh. nodr 28 no.8:15-19 Ag 162. (MIRA 15:8)
1. Urallskoye geologicheskoye upravleniye.
(Ores--Sampling and estimation)

u
H'tl& ~ Ipt
L~'
SFLMY 041"rp='19411 W)
io() kg. UndoA tf Od
ni ro of 0 4110 kS. Lnthnweflc
kq. rc vim rj.&,Co.). and 14
lot) y is WPILrately
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q. ni mnsgue),
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PM,kxwy softc, tc1r, awl to to a 1:
.ctnulJlWdObW"i Affm dwithc Ist Finily.
16

If J_ Y,
_j;?'329. qR(UYLI!G Q~LREPAIRS W1111 FIRE QV OIL URGES USING WERT CASES-
KUDIC4T[. ti. (ftorsk. 56._-~iot-Td-oa Kly. Fleet, Moscow), June
2t-Z3). Ships are equipped with plafit for blowing cooled bollor flue cases
or crigine exhaust gases into the tanks or oil barges and so naking thm
..safe for repair work without cleaning out of the tanks. The conccntr-ation
of gas In the tanks ra=ins sarojor 6 to 12 days. A stozm locwntlyo
1= been sImIlcwly equipped to provide an Inert atmosphere in rall mounted
tanics. (L).
6

"I ;
A.
tesf~arches on the enrIi:r.,mce of r!oncrete-ccramlc el(- -r,-nts. P. '~77.
R
I
Vol 12P no. 11, ~Iov. 1~1~. T'7,T-11';j'?TA T Tjjjjrj'. [- JI I ' : ~~ . 1. n 1,01-a-A .
I ! W P
So: ED-isterii uropown ."ccession. Vol 5, no. 4, April 195()

/7(

AUTHOR-: Ttkin, Ctindidnte of Technical '~'ciences, Kupi,ionov, I.Sy.
,
I
E n j7
ineer C-L -------
TITLE: The P,'nchining of fligh-Strength 1'.!nterinls with 7.Tineral-Cernmic
Cutters (Obrabotka vysokoprochnykh mnterinlov mitieralokera-
micheskimi reztsnmi)
PERIODICAL: Mlashinostroitell, 195P, Nr 12, pp 129-z1

ABSTRACT: Experiments were carried out on finishing "3('Fh(3_',NA" steel
with a mineral-cernmic cutter. It was stated that minimum
Wear of the cutter was obtained by applying the following
optimum geomptry of the instrument: face nno~le- 0 0; chRmfer
angle - 100; chnmfer dimension - 0.5 mm. The r(gults obtained
in lRboratory investigations were tested under industrial con-
ditiona with different parameters. It was stated that the
cutting speed of ceramic cutters exceeds that of hard Alloy
cutters by 50 The described instrument can be successfully
used for semi-rough and fininhing lathe onerntions on
grade steel tempered tip to - 160 to in mm_ There sre
2 graphs, 1 diagram, 1 table and 5 Soviet references.
Card 1/1

S/123/61/00()/023/008/018
A052/A1Ol
AUTHORS- Itkin, M. E., jSuRLdqnov_S,_~...
T17LE: Machining high-strength steels with knives tipped with ceramic-
metal plates
PERIODICAL; Referativnyy zhurnal, Mashinostroyeniye, no. 23, 1961, 28-29,
abstract 23B215 (V sb. "InstrumentaAl. rezhushchiye materialy".
Moscow, AN SSSR, 1960, 128-137)
TEXT. The turning of 3OXrCHA (30KhGSNA) high-strength steel hardened to
6~b '16o - i8o kg/mm2 with a ceramic-metal tool was Investigated at the Kazan'
Aviation Institute. Hollow cylinders turned on 25-kw Shiss-Defriz lathe were
used as samples. 332 (TsM332) plates had -the following geometry: I - 0 0 ;
T = -100; 0~ - 12 0; I - 450; ~0, = 10 0 - 150; ~ - 0; r - 0.15-1.5 mm. The
investigations have shown that Ar'amic-metai tools can be successfully used for
semirough and finish turning; the wear of the knife when turning without cool-
ing should not exceed 0.4 mm and when turning with cooling 0.55 mm, the feed
should not exceed 0.11 mm/rev. A formula ror computing cutting speeds Is recQm-
mended. There are 3 reference3, 3 tables, 6 figures. L. Bozin
[Abstracter's note: Complete translation]
Card 1/i

KNPIDUMA, YE. P.
KUPIDONOVA, Y-'-. P. --"Interaction of Metallic Copper with -lubstances of
Proteinous Origin.~Diasertations For Degrees In Science
and Engineering Defonded at USSR Higher Educational
Imtitutions)(29) Higher Education USSR, Kazan' Chemico-
Technological Inst imeni S. M. Kirov, Chair of Physical
and Colloidal Ghemistr7, Kazan', 1955
SO: Knizhnaya Letopis' No 29, 16 july 1955
For the Degree of Candidate in Chevdcal Sciences

KUPIDONOV, S.S.
Three-unit milling dynamometer with wire piokups. lzm. tekh.
no-.12t2l D 163. (MIRA 16s12)

S/081/61/000/012/001/028
B105/B202
t
AUTHORSt Kochergin,-iS. M., Vozdvizhenskaya, Ye. S., Kupidonova, Ye. P.
TITLEi Texture of electrolytic alloys
PERIODICALt Referativnyy zhurnal. Khimi'ya, no, 12, 1961, 34, abstract
129207- (Tr. Kazansk. khim.-tekhnoi. in-ta, 19030, vyp. 2),
69-7U.)
TEM The authors made an X-ray examination of the formation of the texture
in the electrolytic alloys Cu-Zn, Ni-Co and Cc-Zn. It was found that the
electrolytic deposits of brass which are obtained from oxalate, pyro-
phosphate, and cyanogen electrolytes have no texture. The studies of alloys
with a content of 52-63~6 Ni and 36-48/6 Co showed a predominant formation of
crystallites with an orientation towards the [Oil] axis and partly towards
the [0011 axis, The texture has a high level of perfection, a reduction of
the current density favors the formation of the texture in the direction of
the [0011 axis. It was shown that the composition of the electrolyte plays
an important part in the process of the texture formation. [Abstracter's
notet Complete translation.]
Card 1/1

rIt 4)f GcTleval and Inorf.arlic
Ot' 1111 VMUCS Oll illhibit ,Il Of SUI)Stiffl-lils: :n
paint iq~aillst stool cot-rosioll
V. 15, n(I, -I,
61h;kit'w, :Ac-ol, vfwv(~:~Om, pi, value
0' L1,011,I)i1i'm of ~JI,cl
I vlp~
(2 - t! I i i pi c I
pH wlhw~,, examilled. A ste-,~l pi;lb, re';ir,
~11r, n!A illlmon';od ill j)f t).
I It found that among the ;111(, 0,'~; examined,

KM,rJAJ, A. : KOZIOL J.
Calculation of the decrease In the cost oil individual millig. p. 20
GOSPODARKA Z3-OZ'YdA. 'Warszawa. Vol 6, No. 9, Septem)er 1955
SOURCE: East Euro,)ean Accessions List (EEAL) LC, Vol 5, No. 3 Yxrch 1956

t~--' I -I-O-":;-:-ATA' -,.
Subways - 140scow
The eTeat ring. Znnn. sila no. 2, 1952
9. Monthly List of Russian Accessions, Library of Congress, Tlily-1952 IM. Unclassified.

A U-';~OR3 i Potrov, A. A., Kupin, B. S. lalov/79-28-7-64/64
TITLEt Letter to the nditor (Pistmo v redaktsiyu),On the Order of
the Compound of Water and Alcohols With Vinylalkyl Acetylenes
(0 poryadke prisoyedineniya k vinilalkilatsetilenam vody i
spirtov)
PERIODICAL: Zhurnal qbshchey khimii, 1958, Vol 26, Nr 7,
pp~ 1999 - 2000 (USSR)
ABSTRACT: In the investigation of the compound reactions of the vinyl-
alkyl acetylenes the authors found that the correct process
proceeds contrary to their combination with water, alcohols
and hydrogen halides. In the cane of water and alcohols the
hydrogen is bound to the second atom of the compound system,
in the case of hydrogen halides to the first, This way the
atoms of this system change their polarity in these reactions
(see reaction process in the table). The correct process of
the binding of'hydrogen halides with the vinylalkyl acetylenes
was dealt with earlier (Refs 1,2). The structure of the ketones
obtained in the hydration of the vinylmethyl- and vinyletbyl
acetylene in the presence of HgSO was proved by the hydration
Card 1/3 and the spectral analysia. The s4ucture of the ether2 forming

Luttc-rs to the Editor. On the Order of the Compound 5rj*J/7 9 - 21- 7 - 64 /-64
of 'Rater and Alcohols With Vinylalkyl Acetylenes
in the binding of the alcohols in the presence of YOH at 150 0
with the vinylmethyl- and vinylethyl acetylenes were also
determined by spectral analysis as well as by conversion with
diluted sulfuric acid into the corre3ponding alkylpropenyl
ketones, and by their further reduction into the methyl- and ethyl-
propyl ketones. The spectralanalytical data show that besides the
ethers (1) also the fthers (II) are formed as isomerization
products. There are 3 references, 3 of which are Soviit.
AS30CIATIONt Leningradskiy tekhnologichaskiy institut imeni Len3oveta
(Leningrad Technological Institute imeni Lensovet)
SUBMITTEDt April 7, 1958
Card 2/3

L,, '.to rto the Editor. On the Order of the Compound 30V/79-28-7-64/64
of flater and Alcohols With Vinylalkyl Acetylenes
1. Acetylene-water compounds--Molecular structure 2. Acetylene-alcohol compounds
-Molecular structure 3. Hydrogen halides--Molecular structure 4. Spectrographic
analysis--Applications
Card 3/3
I I - . . I .~
il " - I .-- 11

5~ 3, 4) SOY/20-123-2-25/f-1-
AUTHORSt Petrov, A. A., Mingaleva, K. S., Kupin, B. S.
-7th-i
TITLE: Dipolar Moments and Reactivity inyl Acetylene Hydro-
carbons (Dipoilnyye mominty i reaktsionnaya sposobnost'
viniiatsetilenovykh uglevodorodov)
PERIODICALi Doklady Akademii nauk SSSR, 1958, Vol 123, Nr 2, pp 29d-300
(USSR)
ABSTRACT: The investigation of' the addition reactions of the 10-enin-
hydrocarbons lead to the conclusion that in the molecules of
the vinyl acetylene and n-alkyi aci~tylenes (I!) the electron
cloud is displaced in the direction of' the triple bond (Ref 1).
HoWevier, in the case of the vinyl aliyl acetylenes (111) and
obAe"i'soalkenyl acetylenes (IV) a double polarization of their
inbledules hAd to be assumed which is increased in the one or
the oth6r direction depending on the nature of' the addenda: in
thd interaction with the hydrogen halides the order of addi-
tion proved an electron displacement in the direction of the
triple bond (Ref 2)v however, in reactions with bromine, water
and alcohols it was the direction of the double bond (Refs 3,4).
Card 1/4 This twofold reactivity could have its cause in the weakening

SO V/20-12 3- 2- 25/5c
Dipolar Moments and Reactivity of the Vinyl Acetylene Hydrocarbons
of the polarity of the enin system due to a partial electron
displacement in one direction which is contrary to the usual
displacement in the 1,3-enin system ((111), (IV)). some
phydidal properties or the vinyl alkyl acetylenes tend to show
ktch '&* polarisation Ocheme).' U6'aUthdra measured the dipolar
floadnts of.7 Vinyl allyl acetylenes with the following alkyl
gx.0 up a:.. CH 3 _`C2H5- "C 3H7 -9 x 4H9 ~, C 5HiTl C6H1 3 , and C,H, 7 , as
well'tiO the cis'- and trans-propenyl acetylenes, the iao-
pr6pe7hyl-ac6tylene and the P- tert. butyl -vinyl acetylene, and,
for the reason of compafison, also the moment of the phenyl
acetylene. The following results were obtained: 1) The dipolar
m6ii6nts of the vinyl methyl and isoproi~enyl acetylenes are
considerably lower than that of' vinyl acetylene ku.77 D). There-
by the electron displacement in the opposite direction to the
non-substituted vinyl acetylene was experimentaily proved.
2) The dipolar moment increases a lit'le with the increase o:'
the carbon radical, but then remains about constant. 3) In the
cis- and trans-propenyl acetylenes the electrons are displaced
Card 2/4 in the same direction as in the non-substituted vinyl acetylene.

SOV/20-123-2-25/50
Dipolar Moments and Reactivity of the Vinyl Acetylene Hydrocarbons
4) The bekker-Natan effect can not be directly prov:,d in the
moleGUle of isopropenyl acetylene. Although P-tertbut)i-vinA acety-
lene has a higher dipolar moment than isopropenyl acetylene
this dipolar moment is close to that of' vinyl butyl acetylene.
Thus, the measurement results of the dipolar moments of vinyl
acetylene hydrocarbons proved the concept of' the reaction
mechanism of the addition in the places of the conjugated
triple and double bond, as earlier proposed on the basis of
chemical characteristics. There are 2 tables and 10 references,
7 of' which are Soviet.
ASSOCIATIONi Leningradakiy tekhnologicheakiy inatitut im. Lensoveta
(Leningrad Technological Institute imeni LenBovet)
PRESENTED: July 4, 1958, by B. A. Arbuzov, Academician,
Card 3/4

r,JPTIN) B. S., Cand Chem f3cl (diss) -- "'Me attacl-unent or water alA alcohols to
acetylenic md vinylacetylenic hydrocarbons". 1-x- n I n, 1~ 9 `5 (.%',1 n
gar] , 15 - 1/ PP
111 -ch
UP.her end Inter Spec Muc RSTSR, li~ningrad Ord,~r of Labor !~ed Rnanner T-
Inst Im I.,-.nJ.n,-raJ Soviet, Chair of OrEadc Chem), 200 coples (~:L, "lo 10, 1-~O,
126)

r,1 (7.

OR S 11-0i :1 17
TITT,~:: w] i n Ov: F.i IJ )f C~)nj!~ 'T!,
L V IT- 11 t 111
Addition
I; n

T I r
j i

As to th - addition -)f i,h '3 .)f
-~':;l c.-nju:~-t
+
h,,ldroc,irbons .,tith in u-nil 1,~., r ~j :-,-I
r,ios t 1y boro-i f luor ise rved s r-..tTi lyst Tho
affilia~.ion order of th,~ nlcoho12 rnd 'ho hy!!r_ .--. n 11:-~Itdes
(rjel (;n
similar to thtt of vinyl L 3 :~
t r
of' Wiese rl,-tt,. 1-.,a3 to lv~ 4~,~ ;oi~tn 1 t.hp_t ;.n th- virl-11
alkyl Acct.,,jimcn the addition f wo uld prnc.::-~d :.,I
the unma way as that of hydro6..m Im.1j,le-, Oefz; f3, 9), 1..-!.

umior the for:ie-tion of thu _Iierv~ ctlacro. of t.rr)o :~nll of
(I)
Ca-d lp the Droducts of their r%llyl- or .ir;,vj

Inve.,;l gat i onr; in 'Jir? Fiold of ConjuL-ttod ")y3to~,!s. 3OV/75-2'!-,'-2e~/77
. r
XOVII. Addition 0-1- Alc-c-,*rioln to Vin,-,,l -H.', n~,,3 in Lli~, ~re.-T-mce of
-Hr ",,,-D. B. Killian,
4, f 10) t.) Vl'.' ii- ' !,;r.
on ',-~ -;i,n:!] othyle:nr --!t7] (,n.-, in t,% -;'P;'
R - C.
R-C SC-C.", -CH2. 0 2( 1).
The nuthors obtnin,~O different rorults.- They belirive. th--t the
ar.'ilintion of n1co'holo to viny] ':)ok pl-Ice
primarily according to schame 2. All exuariments tho t
the wMition 04' :-tlcohols to viny! al!cyl acutuylenos took
rlnc-~ at the acutyl-2no bond in oprosite --rdcr ao COmDarod
with hydrogen hPliles. The compnriarm of, tho in,"r-r(~d spectr-
of the ethers obtained fro-.:, vinyl methyl- and vinyl cuthyl
ncc,t,vlonon IF-d to th,~ conlusion ti:,.t they are no homologs
of the srizie t.~,pe. It w.-,a shown thrt tho initinl productq of
the above -ffilirttion un,lnrgo icome-rization with rlirr-n,~7,emomt
(-,f thc.- vonju,-'~Jii.-m :jy--t.-,.n of th,~, br-,nd!;. 7he ~Iifforen.-,~s in thn
affiliation order of alcohols anul lv-drogen arum
interpvitol by the concepts regarding the nucleo,,)hilic r.,nd
Card 2/" electroPhtlic witure of thf- itt'filLfition r,~~..ctionj.

lnv03tigations in the Pield of Conjugnt,)d 5C,!1/7' -71-- '--,rl/77
XCVII. Addition of Jlcohols to Vinyl- lkyl-r.cetyleneo in l.'ac Prc,3,2ncc oi
Koll
5 S(, 0 1 AT 1, ,N 1,vninlrr,rnl,)kiy tel-hnolog-ichooki,., inniAlut
(LuningriO Technologivil InsUimto
SUKUTTED: Februnry 28, 195S
Card 3/3

5 (3)
ATITHORS: Kupin, B. S -2
~Ltrov, A. A. :,0V/79-29-7-39/83
TI TLEt Investigations in the Piold of Conju,,,,ate Sj,otc_,j_,, (I_,sjeL'cvUni3'a
v oblasti sopryazliennykh iiutem). CII. On tho Diroction of
Hydration of Vinyl Alkyl Acetylenes (CII. 0 napravlenii
gidratatsii vinilalkilatsetilenov)
PERIODICAL: Zhurnal obshchey khimii, 1959, Vol 29, Ur 7, pp 2281-2284 (US!',q)
ABSTRACT: In the present paper the hydration of vinyl methyl-, vinyl
ethyl-, vinyl propyl- and vinyl butyl acetylene was carried out
in the presence of mercury combined with sulfuric acid. In each
case the formation of three isomeric ketones could be expected,
the constants of which differ very abruptly:
R-CH -C-CH=CH
2 2 M
R-C -C-CH=CH 2 1, R-C-CH 2- CH-CH 2 (1')
8
R-C-CH=CH-CF.3(111).
8
Card 1/3 Thus, however, alkyl propenyl ketones (III), with admixed alkyl

r,O
Inyeatigations in the Field of ConjuC;atc "J'yatems. j '1/79-29-7--39/83
CII. On the Direction of Hydration of Vinyl Alkyl Acetylenes
allyl ketones (II) were mainly obtained. The structure of the
ketones was determined b comparison of their constants, and
infrared spectra (Fi ~y by mearis of publication data an well
as by investigation of the saturated ketones forming from them
by hydroganation. The constants and infrared spectra of the
synthesized mothyl-propenyl-, ethyl-propenyl- and propyl-propanyl
ketones are closely related to thooe given in publications
(Refs 11, 12). In all spectra the i;rouping -011=CH- was proven
by the intensive frequencies in the ran-e of 970 cm- 1- The
hydrogenation of all hydration products over Pd/CaC0 3 mainly
led to the alkyl propenyl. ketones described in publications
(Ref 12). The affiliation rate of water decreases with the
enlargement of the hydrocarbon radical, which caused that the
reaction be carried out at heating. The .n=or of afi-iliation
of water and alcohols to the vinyl alkjl acetylenes accor(ling
to reference 14 does not correspond to the mariner of
affiliation of hydrogen halides, which may base on the fact
that these reactions take place differentlY. There are
Card 2/3 1 figure and 16 references, 11 of which are 9oviet.
6
iq

InveBtigations in the Field of Conjugate Systems. S0'[/79-29-7-39/83
CII. On the Direction of Hydration of Vinyl AlIV1 Acetylenes
ASSOCIATION; Leningradakiy tekhnologicheskiy institut imeni Lensoveta
(Leningrad Technological Institute imeni Lonsovet)
SUBMITTED: June 18, 1956
Card 3/3

50) :;(.)'1/7) -~) -~-75/76
AJTRORSt Petrov, A. A.
TITLE- Letter to the Editor. On the 11Z.,drat-ion Order of Jnayimctrical
Doubly Substituted Acetylenes
P ER I UL ICA L jZhurnal obshchey khi~aii, 1959, Val 2~, Nr 9,
pp 3153 - 3154 (US3R)
A B ST C T The monosubstituted acetylene hydrocarbons, among them also
alkenyl acetylenes, result in methyl-alk~~l- (or alkenyl)-
ketones only when hydrated under the, reaction conditions
suggested by Kucherov (Refs 1-3). Accordingly, vinyl-alkyl
acetylenes should result in alkyl-vinyl k~.Aones, however, they
add water quite irregularly under the for-Ination of alkyl pro-
penyl ketones. On the basis of theQretical considerations, this
order of hydration can n~;ither be explained by the 1,4-addition
of water nor by polarization of the molecules of vinyl-alkyl
acetylene under the influence of radicals. To find the causes
for the hydration direction of vinyl- and divinyl acetylene,
the direction in which water is ad,,ed to the si~tplcst ir,--thyl-
alkyl acetylenes was inveotig5t,d by Kuch,-rov's react'-on.
Comparable data on these problu,no have not yet been dealt with
Card 112 in publications. The compof3ition of thi.- ketone mixtures was

Letttr to the Editor. On the Hydration Ordur of Unnjwi~etri- 30/79-29-9-75/76
cal Doubly Subutituted icetylenes
determined by comparing the intensity of thQ characteristic
frequencies in the infrared spectra of the hydration products
to that in spectra of artificial mixtures with a known conteut
of each of the expected kutonoo. The results are indicated
in the table. Thus, the dependence of the order of hydration
upon the structure of the radicals is proved. There are 1 table
and 5 references, 4 of which are Soviet.
AS-SOCIATION: Leningradskiy tekhnologicheskiy institut imeni Lensoveta
(Leningrad Technological Institute imieni Lonsovet)
SUBMITTED; May 25, 1959
Card 2/2

S/079/60/030/007/038/039/XX
BOOI/BO66
AUTHORS: Petrov, A, A- and.KuRin,_D. S.
TITLE: Mode of Addition of Water and Alcohols to Vinyl Acetylene
Hydrocarbons
PERIODICAL: Zhurnal obahchey khimli, 1960, Vol. 30, No, 7, p. 2430
TEXT: The addition of water under the conditions of Kucherov's reaction
is analogous to that of alcohols in the presence of KOH to vinyl alkyl ace-
tylenes and corresponds to the theory of electron displacements (Ref. 1)~
But to isopropenyl alkyl and vinyl isopropenyl acetylenes water does not
add according to polarization, as might be expected for these hydrocarbons.
This anomalous mode of addition may be explained by 9teric hindrances in
the intermediate formation of a mercury complex (under the conditions of
Kucharovlu reaction, assuming that the reaction has an electrophilic
character In the first stage (a radical on C 3 hinders the access of mercury
to C2) . To confirm this assumption it had to be shown that the mode of
addition of nucleophilic reagents, such tie mothyl alcohol in the presence
Card 1/2

Mode of Addition of Water and Alcohols to 3/079/60/030/007/038/039/XX
Vinyl Acetylene Hydrocarbons BOO1/Bo66
of KOH, takes place without catalysts (heavy metals) according to the
general rule. The addition of methyl alcohol to isopropenyl methyl acety-
lene in the presence of KOH gave an enol ether boiling at 67--720 which,
on hydrolytic cleavage with dilute sulfuric acid yielded mesityl oxids
which contained no ethyl-isopropenyl ketone impurity, On hydrogenation
with Pd/CaCO 3 catalyst, mesityl oxide ga%e a methyl isobutyl ketone, which,
according to the constants, the infrared spectrum, and the melting point
of the 2,4-dinitro-.phenyl hydrazone, was identical with a methyl-isobutyl
ketone sample of known composition. It was found that the mode of nucleo-
philic addition of alcohol to isopropenyl methyl acetylene differs from
that of water under the conditions of Kucherov's react-ion, This confirms
the previous assumption regarding the mechanism of this reaction and the
causes of anomalous addition of water. There Are 3 Soviot referenceB..
ASSOCIATION: Leningradakiy tekhnologicheskiy inotitut imeni Lenooveta
(Leningrad Technological Institute imeni Lensovet)
SUBMITTED: March 9, 1960
Card 212

24819
S/C)8 61/000/0-1015/040
B105/B203
AUTHORS: Kupin, B. S., Petrov, A. A., Yakovleva, T. V., Maslennikova,
'1-. G.
TIT L L Dlre:tion of hydration of as~,mmetri-2al 1-,jubatituted
PERIODICAL: R,~-ferativnyy zhurnal. Khimiya, no. I! , "t")1 , 176-179.
abotract 11148 (Tr. Leningr,. tekhriol. in-ta im, L,~nsovt-t~i,
196t), vyp~ 60, 63-69)
TEXT: The authors studied the addition of water under the conditions -~f
reaction on CH 3C a CR (I), where (a) R - C,'J11," (b) R ~ C 5H7
R ~ (CH CH, (d) R - (C11 C . A notl2eable ori--nting effent is only
2
c,bserved in case (I d) (65~o ethyl-tert-butyl ketone and 35,"j Mieth."I neo-
ponty) ket,c)ne) The -?th-ir hydrocarbons give mixturoo of a ,I po3siblk~
k9tones at ~jbc~ut ?qual ratioB, Thp ketone mixtures were analyzed by
-.Orrparin6 the.,r infrared spectra with spectra of rrixtures ~f known
f~ornpositlun. The maximum error of this method It was found that
th~- order of add,.tion of water to d1subBtituted acetylenes is determined by
Card 1/5

2019
S/08 6!/000/01'/015/040
Direction of hydration of asymmetrical B1,05403
at least, two factor3 acting in opposi-~,j directions: by the polarization
We t- j ,,i-~rjupi ing of the aretylene bond and due to industior polarization.
Th- ~f fe~-~ ~ f !31,~ir I - fa: t-ro 13 P~.)35 Ib 1 0). (1 a) was obtained b,,,, the effect
Nal Q It, I 1 1' % qu i d 1111
N11- ar da -w a rd a f t h,! -i I-Ii -Y 1 1- r vir. -. d er CCC it
Ar, i x ture g -.~ f ( 1 4 g o f I1k;O g - fFe, /so') and 250 ml of
'I
0'/4 1] S C) was stirred fe.- 5 hr, saturated wi.h ~'141114 )~)SG,4 ,and 8.2 F of the
4 - ?0 ?0
k,-t,,nP mixture was obtained (boiling point 10'-',0l -50C, "- D 1 .3920, d4
0-.~096). By ne-ans of hydration of (I b~ (10 g) :Iobtain-~d frDz- C3H7C uCNa
ctnd CH 13:- in 11,1-.;,.d NH '5 g of ketone mixturp were obtained (boiling
"C n 0
i~' . 1 4 . The hydration of 5 g of
,.!nt 123 5-12445 29D 1~4020, d 0~8133)
(I c) (synthesized from CH31 and (CH 3)2 CH-C a C11, the latter obtained from
(CH3)2CH CH2 CHO by action of PC15with subsequent separation of HO by means
of alcoholic alkall. solutiop at 140-1500C yields 2.8 g of ketone mixture
(boiling point 114-1150C., n40D 1.3972, d ~O 0.8020). To the solution of
4
Card 213

2)1819
S/ob 11/01 a/O~~O
Direction of hydration of asymmetrical B'05X32034
of HgO in 260 ml of 14-11) H,,SO 11 g of (I d) (obtained from tert,
e 4'
of 'h'?
t, -, a i n;~d a f to-, 6 ii 1 t !-.r, i n t I C . n 'D 7 J V
R ordor of
CH and C(Cll,),V FA change in the ~lrder of addat;-,n 3 rct
Rb3truo'erts not-.~: Comp] e e , rans!
"ard V3

KUPIN, B.S.; PETRCV, A.A.
Investigation in the field of conjugate systems. Report 124:
Direction of the hydration of isobuten~rlacetylene (4-methYl-3-
penten-1-yne). Trudy LTI no.60:70-74 160. (MIRA 14:6)
1. Kafedra organichaskuy kbimil Leningradlakogo tekhnologicheskoso
instituta imeni Lensoveta.
(Hydratim) (Pentenyno)

KUPD.1,-B.S.; FE'TROV, A.A.
Con.lupntrd vyntemn. Part 1431. Vlroal.ion of thf- hydration of
alkylpfienylacetylenes. Zhur.ob.khim. 31 no.9:2956-2965 ~; 161.
(MIRA 14:9)
1. Leningradskiy tekhnologicheskiy institut imeni Lensoveta.
(Acetylene) (Hydrntion)

KUPI14, B.S.; PETROV, A.A.
Direction of the hydration of asymmetric methylalkylacetylones
in the presence of sulfuric acid, Izvevys.ucheb.zav.;khim,i
khim.tekh. 5 no*3:439-4AI 162e (MIRA 15:7)
1. Leningradskiy tekhnologicheskiy institut imeni. Lensoveta,
kafedra organicheskay khinii.
(Acetylene) (Hydration)

KUPD, 1'ETWV, A,A.; KOPTEV, D.A.
Conjugated systems. Part 1"8-- Hydration of somne enynes and dienyneB
with allyl radicals. Zhur.ob.khim, 32 tio.6!1758-1761 Je 162.
15.,1
1. Leningradskiy tekhnulogicheakly institut im. b-ningrz: 'dr~kogo Zo-;,,tn.
(Hydrocarbons) (Unsaturated compounds) IFydration)

KIJPDIP B.S.; PETROV, A.A.
Conjugated systems. Part 159: Hydration of 2-hexen-4-yne and
3-cathyl-2p.hexen-4-yne. Zhur.ob.khim. 32 no.8:2494-2498 Ag
162* (MIRA 15:9)
1. Leningradskiv takhnologicheakiy institut imeni Lensoveta.
(Hexenyno) (Hydration)

KUPIN, B.S.; PETROV, A.A.
Direction of the hydration of asymmetric dialkyl- and alkylarylacetylenes
subjected to the action of formic acid. Izv.vys.ucheb.zav.;khim'%i
khim.tekh. 6 no.1:75-77 163. (wRA 16:6)
1. Leningradskiy takhnologicheakiy Institut imeni Lensoveta, kafedra
organicheskoy khimii.
(Acetylene compounds) (Hydration) (Formic acid)

PETROV, A.A.; YAKOVLEVA, T.V.;,KUPDI, B.S.
2,3p5-Trimethyl-l-boxen-3-Tne. Zhur. ob. khim. 33 no.5:1701-
1702 My 163. (MIRA 16:6)
1. leningmdskiy tokhnologicheskl inatitut imeni Lonsoveta.
(HexenyneT

KUPIN) B.S.; IIETI(OV, A.A.
Course of the hydration of dioub3tituted acetylenes. Part 1-1:
Hydration of isopropyl tort-butyl-, and Isopropenylallylacetyleness
Zhur.ob.khim. 33 no.12;3860-3863 D '63* (MIRA 17:3)
1. Leningradskly tok-linoloricho.;kly Imititut J-.~e,,jj Lensovota.

F,U I I. NY 13. J,. *p I,, 'I I, , '~ .
courof~ c,,t* 1,1 ;.;t icorl c,,' c.1 cohols , ~?- t,,- - '-' '-?' ~',' ' - V~ .
! 1- ~l " I.,, .
i.. & I ~ 81P
- bu r ob. K~ilr- 14 rn-t- -189) J` ';' .
I - 1. vt` .
- T~".m ~4, !, , .

KIIIINY IIXTI(OV, A,A,
--'-7i.t)urvo oi' the Ilucloophilio dddition or ionronpWns L) IP3
hydrocarbonn. Zhursorg.khims I no.2:241.,.248 F 165. (YIlIA 19:4)
J.. LAningradakly tokhnolool cite oki-y inatitut imani Lo no ove tA.

KUPIN, B.S.
Hydration ecurse of disubstituted acetylenes. Addition of water
and methanol to &lkyl and alkanylphonylacetylenes. Zhur. org.
khim. I no.7c120&-1212 il 165. (MIRA 3.81ll)
1. Laningradrskiy tekhnologicheskiy inatitut imerd Lensovett.

1. KUPIN, I.A.
2. USSR (6oo)
4. Motion
7. Determination of the finite region of initial deflection tit which motions remain
asymptotically stable, for systems of two equations of the first order. Prikl. mat.
i mekh. 16, no. 5, 1952.
9. Monthl List of Russian Accessions# Library of Congress, Februar 1953. Unclassified.

GOLIDI,Wl, A.M., kand.khimichoskikh nauk; ZAYTSEV, A.I.; KOSTYILV, G.I.;
1AYWLANCOK, L.S.; LUDYANITSKIY, I.Ya., kand.khimichesklkh naiik;
J'1C,,ObRAZ1BNSK1Y, V.A.; FUf=N, M.S., doktor khimicheakikh nauk;
Prinimali uchastiyo: ZHADIN, B.V.; VESELICHAKOVA, T.L.; SEDOVA, S.M.;
TRUBN1KCJVA, V.I.; KUPIN ji-j-.; ZMOVA, Ye.I.
Preparation of adiple acid in a continuous pilot unit.
Khim.prom. no.5-.323-327 My 162. (MIRA 15:7)
(Adipic acid)

KUPIN, N.
Hydraulic gluing press for joinery. Strottell 2 no.2:11 7 156.
(joinery) (mm 9:12)

KUPIN, N.V.) inzh.; SHABOVTA, V.V.
Special electrode holder for spot welding machines. Svar.
proizv. no.1103-34 N163. (RIRA 17:5)

KUP-*'-Nv N.V.P it"711.
Yffic-..ont eleotrrAi rizon for tpo, wtl~c:ll? -," '-' ,
I \
proizv. no.9437 :', 164, -'7~12.,
1. Tyumenakly mudoatroitellnyy zavod.

inzIl.
Book reviejs rind 'bibliography. Svar. F
(:,t!I'I',-. 18:,3 .)

-1, P.-C In I __ __
ACC NR1 AP502WI12 E,'J.,%(c) lip(c) SOURCE CODE: UR/0229/65/000/010/0055/OCO
MOTI/M/1W
AUTHORSt Xupj!!j_X'_V.; Kalinino N. Is; ShtW!r_2_V1j!.J~
JA
ORG: none
TITLE: Spot welding of aluminum alloys with low-power machines
SOURCE: Sudostroyeniye, no. 10P 1965P 55
TOPIC TAGSt spot welding, aluminua~llloy, welding electrode/ STE 34 electric
transformer, MTP 150 welder, AMtaAM aluminum alloy, AMg6M aluminum alloy, D16AT
aluminum alloy, D16AM aluminum alloy
ABSTRACT: Experience has shown that the low-power,MTP- 150 spot-welding machine can be
redesigned for aluminum-alloy spot-welding installations. The power of the machine is
increased by connecting an STE-34 welding transformer as a booster in its primary
circuit. It is suggested that the AX203 film be left on aluminum alloy parts to be
Bpot-welded with low-power machines, since its presence facilitates heat removal. It
is advisable, however, to remove the film from the electrode side of the part, since
this reduces the contact resietance. The use of a special electrode (see Fig. 1)
makes it possible to produce 25 to 30 spot-welds without cleaning the electrode.
Electrodes with diameters of 7-5, 8-0, 8-5, and 9-5 Em should be used for welding
metala I.Or 1.2, 1.5t and 2.0 mm thickv respeotively. Redesigning of the IATP-150 made
Card 1/2 uDc, 621- 791- 763- 1 s669.71

ACC NRs
--4
---- ------
Fig. 1. Shape anO siv~/bf electrode.
6
it possible to weld AMtsMv JU%,6Xp D16A~~D%jd~and other aluminum alloys with
thicknesses to 2--2-5 mm. Orig. art. has: 2 diagrams.
SUB CODEt 13/ SUBM DATE: none/ ORIG REP' 003

1 ?
KAGANCNIGH, "'J! --0 A,-, ~ ,- Y u C t,- I c I, f Vard-, . I'i-, Ic i i n . , i t nj k p 6 o t'.9 . ; K I F III I ,
. J, - rophor')VIch) irzh. ; KI, 2. -11 "A I ". IF a ) r(d.
(Calcultitlon arvi constructi,;n of floxible pavements;
nyst.oriatic manuall Ranchot i konitruirovanl(i nezieotkikh
dorozhr~-',h c)ciozhrl; notoullehfin~oo 7losoble. Orisk., 7auadnc-
SJbirokne kni-zlinot) T)64, ", V. (Mbliotaka .stu-
dfinta, 110,0) lp:g)

,hP 111GOE
17

ALEKSEYEV, F.K.; ANDRIYUTS, G.L.; ARSENTOYEV, A.I.; ASTAFIYE;V, Yu.P.;
BEVZ, N.D.; BMWVSKIY, A.I.; GENERALOV, G.S.;
DOROSHENKO, V.I.; YESHC.HFNKO, A.A.; ZAPARA, S.A.; KALINICHENKO, V.F.;
KARNAUSHENKO, I.K.; KIKOVKA, Ye.I.; KOBOZEV, V.N KUPIN V Ye
LOTOUS
I V.K.; LYAKHOV, N.I.; MALYUTAO D.I.; WTS -ru:S,-; 1070,; Dmq,
B.K.; OKSANICH, I.F.; PANOV, V.A.; PCVZNER, Z.B.; PODORVANOV, A.Z.;
POLISHCHUK, A.K.; POLYAKOV, V.G.; POTAPOV, A.I.; SAVITSKIY, I.I.;
SERBIN, V.I.; SERGEYEV, N.N.; SOVETOVt G.A.; STATKEVICH, A.A.;
TERESHCHENKO, A.A.; TITOV, O.S.; FEDIN, A.F.; KHOMYAKOV, N.P.;
SHEYKO, V.G.; SHEKUN, O.G.; SESTAKOV, M.M.; SHTANIKO, V.I.
Practice of cozIstruction and exploitation of open pits of Krivoy
Rog Basin mining and ore dreBsing combines. Gor. zhur. no.61
8-56 je 163. (MIRA 16:7)
(Krivoy Rog Basin-Strip mining)

KUPINA) N. A-.) Cand of Chem Sci - (cUss) "Tensimetric and thermochemical atudly of
&queous solutions of the electrolytes (NaCl, NH4C1, Me12,, COG12)-' laniWad, 1957,
14 pp, (Uningrad Technological Institute, Chair of Ptwoio&l Chemistry),, 100 copies
(KLI 29-57#89)

Win
M-'
-Sn
-h RM, R~

B-11
Solutions)' Theory of Acids and Bases
,jSSR/Fhysical Chemistry
No 2) 195% 3926-
Abs juur: Referat, Zhurnal 1(hm'yal
Author : nstitute of TechnolOgYi JAningrad.
Inst :IiL'~e-; %-ns. ~omv , t ~In s tind Thermochemical Study of Aqueous solutions
Title :TenBimetrical (COC12, NH4Cl, VaCl, MgC12)'
of Electrolytes im. Lensoveta, 1957, vyP. 40,
orig Pub: Tr. Jeningr. tekhnOl- in-t&
92-111.
e on the solutions COC12-H20, NaCl-He and
Abstrw2t: The vapor Pressur as well as that On the
C,_H20 at -6., +2., 18., 25 and 500
NH4 +2 and 2-56 'was measured by the statis
MgCl2_H2p solution at -6s The following
_ method over a wide concentration range.
tical of dissolution and specific heats were determ-
int,egral heats solution (c = oA up to satuxa-
ined: at +20 of the 1M4C1_H2 ) UD to saturation) and COC12-
tion), at -60 of 104cl'.H~D (c - 2)C I f COC12 solutions
HP0 (c = 1.0 up to saturation). The densities o
card 1/2
USSR/irnysical Chemistry - Solutions, Theory of Acids and Bases. B-11
Ab s J ou r :Referat. Zhumal Xhimiya, No 2., 1958., 3926.
0
in water were measured at -6, +2, 25 and 50 . The partial molar
thermodynamic characteristics of the above mentioned solutions were
computed. It was shown that the crossing of specific heat iso-
therms of a salt f(c) in the range of the complete solvatation
border, denoted b~i.;. Yakovlev in the cases of NaCl solution in
H20, was also characteristical of the solutions studied by the au-
thor. The specific heat isotherm c. Of COC12 solutions at -60
is situated in its major part above the isotherm of +20, which, in
the author's opinion, is connected with the existence of a crystal
hyd.-ate in this temperature range.
Card :2/2 -2-

L 3583o-66
I-AeCkr-
3 S01DRCE CODE4 UR/0243T6576-DoTo 16-/65-9 1
AUTHORS: Artamonov, B. P. 6 t
ORG: Leningrad Chemico-I'harmaceutical. Institute (Leningradskiy khimiko-
farmatsovtichookly institut)
TITLE: Conductometric analysis in the manufacture and inspection of chemicals and
pharmaceuticals. 4. Ionization constant, conductometric determination of Tubazid
SOURCE: Meditainskaya promysh..ennostl SSSR, no. 10, 1965, 61-63
P//A e flm I Cro r., C-9 IL
TOPIC TAGS: quantitative analysis, ionization potential, ph meter, hydrochloric acid#
dissociation4constantI LPU-*01 ph mete , Tubazid Py*9eern,4veLrr1c-,9X-
1)~- NO
ABSTRA(r-,; The ionization constant of Tubazid is determined, and conductometrio
determination of Tubazid is studied. The work was done because of the defects of
existing methods. An LPU-01 p1l motor with an error of t0.04 pH units was used. All
measurements except those with conductometric titration were done at 25 10.02C. An
experimental check showed that direct criductometric determination of Tubazid is
possible, owing to its hiCh pKb (nee Fig. 1). It wan established that the PKb Of
Tubazid at 25C is 10.62 t0.02 GK = 3-38 +0.02). It is recommended that inverse
nolat,
conductometric titration of u onn of Tubazid in hydrochloric acid be used as a
method of accurate quantitative determination.
Card 1/2 uDc: 619.724.8-014.3:943.257.

L 35830-66
AP6004903
ml)
Pig. 1. Inverse conductometric titration of solution
of Tubazid in hydrochloric acid.
Orig. art. haot 2 tablesp 1 formulap and 1 graph.
SUB CODEs 06, T/ SUBM DATE: 29Apr65/ ORIG REFs 004

YUGOSLAVIA/Cheraical Technology - Chendcal Products and Their 11-17
Application. Medicinal Substances. Vitamin3.
Antibiotics.
Abs Jour : Rof Zhur - Khitaiya~ No 17, 1956, 58423
Author : Carubolo Ivl, Kupinic Mirjaiia, Radisevic Ankdca
Inat : -
Title ; The Stability of Antibiotics in Em, sions Containing
Water and Their Preparation in Pharmaceutical Practice.
Report I. Emulsions with Penicillin.
Orig Pub : Acta. pharranc. Jugosli~ 1956, 6, No 2, 105-113-
Abstract : The activity of penicillin (1) in an aqueous solution of
buffer citrate Na-nipagin or -chlorocresol during a 40-
day storage at 20P, is preserved up to 81% while Li
emulsions of the oil-watcr type where the aqueous phase
is a bath of I in a sterile solution of citratc lia-nipa-
Gin, it falls In 15 days to 10%; in those prepared
Card 1/2

YUGOSUNIA/Chemical Technology Chemical Products and Vneir 11-17
Application. Medicinal Substances. Vitamins.
Antibiotics.
Abs Jour Ref Zhur - Khimiya, 110 17) 1958, 58423
anceptimIly after 15 days, It falls to "., cLn(I in
rmn,Llsions of tlic water-oil type for 15 days, the acti-
vity of I flalls to 25%; while in those prepared arcc,,)-
tically to 10%. The pff of nonsterilized emulsions Is
5-5; of storilized., 5.3- Hence both types of cmul-
sions are recomended for the full utilization of the
activity preserved only for 15 daYs at 20P.
Card 2/2
- 48 -

"MOSUVIA
CORUTOLO, Ivo; RAMSEVIC, Ana; and of the Republic
Public Health Institute (Republicki Zavod za Mravstvenu Zaetitu)
and the Croatian Medicine Testing Institute (Zavod za ispitivanje
Lijekova SRH), both in Zagreb.
"A Contribution to the Problem of Obtaining and Preserving
Distilled Water in the Drugstore."
Belgrade, Narodno Zdravlje, Vol 19, No 7-8, 1963, pp 253-258.
Abstract: ZA-uthors- English summary modifieg Scmplos of dintil2od
water from nur.OrOI13 dx-ugstores have proved to be contaminated with
micro-organisms to a high degree. The authors UrEG special precau-
tions during -the distillation process and in storage and suSCest,
that each drugstore prepare its own distilled wator in glass con-
tainors not in excess of 10 liters' capacity to be kopt no longer
than bieht days. The authors listathroo t,,1Tuu of di:itillod water,
viz., that proparod as abovog froshly boilod, and that uood in in-
jections. Ti-fo tables, eight references (mixed Western and Yugo-
7 slav).
~7
29

-g
~

0 0 a * 0 0 0 0 410 0 0
0 0 0 0
o 0 0 ~06 0 ~00 40? ~0~
I to to If It 11 11 a 411
J1
6 a 11 6 1 it a
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(A 9 u
Iv,

-
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a*
K PC lead, d(Ild, 11411. 1'. it, N S
-
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;

of Al sit
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or lo
if
*wt ord I ~v -1. 1 a
go IIAIT.I.
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t W Whe" is m4wil .4" .' i I
v I'm .6,11Y vv.n :
I
.
w Most I lie Alms) valut in j onin , 1".
,
isiorrifictilis Inside its l1w Im list" give valtw4 wKfwwhaf 401

ow she Milli valtw. The rate to thirtrivne rallM Wit -a*
ft. 14
if
see
'3

00
goo
Of to a 00
too
=00:

00 zs
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logo
00 A &lIAtLLlf4,KA1 1,111111611" CL.ISW.C.lOC. to~ 0
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fi-j-t
Ass I I a NO 0 IF -11- a,
u n Is, If no or ff 11111 to it Is Is
a 0 0 0 0 * 0 0 a 0 a 0 0 0 *I s 0 a v a 0 0 c a 0
0 0 0 0 0 0 0 0 0 0

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------ TA-4

M~ for Swe"radoo of cWO(O4C6t*a4'
IW CA
k
A
J
rm.
.
P. A. Shnov mW (P. V. Kupins
PP
ay:.
Is
1r
id
ed
m
i
u
pp.
the tab. ctmfinums hif a 0( jjrC0 in Ithich the, .00
-tqm;'tAlv I "Aunin.
a water-jacketed ttIvp
is I
t
.
s m
n
reagm
wahin
-ah
effected b
-00
l b
f
JICI
h
rermova
e
og
the
wit
y
j
Cutird. CAC16 viln. thl" chloorinallim i, vatiw~l unly to
.0
d
i
99
V
s
,
uct
,. rAlre
W-79%. tht Pro
The prodwt. after washing, it Its, tittmt"L CoO, .4n .00
j is reStswated by nArble. Yiekl% range Imm Ll ji) I '.'h
fro 0
hil. pn4o" Per I ks. acrtme. G. M. X~x[Apoff
4
t

go

S. I A SITALLAIRSKAL LITINATURE tLAISMICAIM I jr- - tie*
spew 17"0111.
k4a 0.1 ON "LOI low- stili I GIC a-I&if
b u
0 a 91 loopill fad 1919 m a Is if 0 a 2 1 At 0 0 AS 0 >
a MAO
0 0 91
*00 :_ 0 00 -0 0 0 0