SCIENTIFIC ABSTRACT PLISKO, A. P. - PLISOV, A. K.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001341310011-6
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: August 23, 2000
• Sequence Number: 11
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

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PLISKO, G. [Pluska, JQ, vrach
Combined cardiac insufficiency. Sa-aka i sb7ttia 10 no.6:
35-16 Je 160 (MIRA 13:7)
(MRT SAIJEM)

PLISKO JODO
Dendrobasna. auriculata (Rosa., 1897) a new species of earthworms
(Oligoehaeta, Lumbricidae) for Poland's fauna. Bul Ac Pol biol
10 no.2%61-63 162.
1. Zoologisches Institut, Polnische Akademie der Wissensche-ften,
Warszawa. Presented by T.Jaczewski.

ANDREYEVSHAYA, G.D.,, kand. teklm. nauk; FLIBKO,, T.A,, insh.
S=e PhYoical Properties of continuous basalt fibers. Stak.
i ker. 20 no.8s15-18 Ag 163. (MIRA 161l1)
lo Institut khimichoskoy fiziki AN SSSR.

PLISKO. J-.D-.
A m6klmation. of finding a new specieo of Dendrobaena platyura
(Piu.) var.-montana (Cernosv.) (Oligoehasta, Lumbricidae).
Bul le Fol bi6l 10 no.6:229-231 162.
1. Zoologioches Institut, Polnische Akademie der Wisoenschaften,
Warsawa. Presented by T.J'aezevski.

'--- PLISKOI J-. 1).
Vejdxvvskyv 1876., a younger synonym of the name Lizabricus lucens Waga,
1857 (Oligochaeta, Lumbricidae). Bul Ac Pol biol 9 no.2:101-10/+
161.. (Em 10:9/10)
1. Iikstytut Zoologiesny, PAN Presented by T. Jaesevski.
(OLIGOCRAETA) (EARTHWO M )

PW-tMf V., inzh.
Orl,anizing rf.)utir:F~ cl.eck rn3 r~Ipajr op--ratzion~,
sc-(:+ions in a rr-js.-3enc,,---r tramipozz-Vition rNt. 4"i
no.9-21-21 S 165. 0-1-%"~ )C,-1
I'! it, ~ . ,,I)

PLISIO. V.;

_1-168~4-66:-' ~E EWP (l B/r;t4
h
ACC KR UH1
P31sko, V.
a 1 CmI)u rs (Elementy tsifr~dvykh mashin) - Moscow, Voyeni-
Elementii o JA ial c te
e
0159 A I I iiii biblio., 11,500 ccr-d s printed.
-TOPIC TAGS -electronic cozputer,,~ digital computer, computer component electron
Wbep seiiiedfidtici!.or I device, ferrite core memory
:.-PURKSE I- -ANDICOVMLW-.' The book.discusses the pri .nciples of operation and the s -elec-
tjob ~of_parameters for. electron -tube elements, semiconductor devices and ferrites,-
used An electroW,'C digital -computers. ~ The bobk describes specialaspecte-In the
of.baste -Computer blocks-and the characteristics of parameters of the
__IWic attention is given to examples.for the calculation of electro-
elements used.
--nic -digitaL compi"r elements on-the basis Of :giVen- characteriaticso The--book is - -
Anitended for technical personnel engaged in.the operation-and maintenance ofelec-
tronic interested in the application
digital.'cikVuterB as vell as for readers
..-of. prin4ples., of 'I; radio electronics in computer technology.
abridged):
TABIS OF, COMM~
'M d* hataiaiikitiig OfAelectronic digital compute
prilao*bliis of ~Opera oil an :C rs
Q*- no Elec: roni:
t ~tube elements

, PLISKO, V.A.; PLATONOV, S.A.s polkovnik, red.
[Elements of digital computers] Elem-enty ti-jfrovykh
raishin. Moskva, ~oenizdat, 1965, 159 p.
(MJRA 18:9)

PW=.-,T&k1v#y,Autonovi&;. PLATONOT. S.A., polkovnik, red.; STRMINIIOVA,
.N.A.. takhn.,red.
Ellectronic equipwat in military science] Zlektronaye mashiny
v voonnox dole. Koekva, Toon,izd-vo N-va obor.SSSR, ig6o. 74 p.
(MIRA 13:5)
(Blectronies in military engineering)

CHUGAYEV,Yw.-ly Gennadiyevich; PLISKO, Valeriy Antonovichj BAVAROV, V.A.;
BOL I SHOV, V.M. ; GRACHEV,~--g A. I.;
PLATONOV, S.A., polkovnikp red.; MEDNI*DVA, A.H.p tekbn. red.
[Electronic digital compaters)Elektronrye tsifrovye vychisli-
tellrqe mashiW. Moskva, Voenizdat, 1962. 405 p. (MIRA 16:1)
(Electronic digital computers)

ASE I BOOK EXPLOITATION SOV/6293
Pli
Chugayev, Yuriy Gennadiyevich, and Valeriy Antonovich Plisko
Elektronnyye tsifrovyye vychis lite 11 nyye mashiny (Electronic Computers).
Moscow, Voyenizdat M-va obor. SSSR, 1962. 405 p. 17,50G copies printed.
Resp. Ed.: Yu. G. Chugayev; Ed.: S. A. Platonov, Colonel; Tech. Ed.:
A. 19. Mednikova.
PURPOSE: This book is intended for military personnel graduated from
special military schools and concerned with the operation of electronic
digital computers, as well as for technicians and persons desiring to
learn the construction and operation of these machines.
COVERAGE: The book describes the design and principles of operation of
electronic computers, based on element, unit, and deviate circuits now
in use, but without giving a detailed description of specif.c machines.
As the book is supposed to assist military specialists in their daily
Card 1/0'

Electronic Computers (Cont.)
SOV16293
activities, it does not deal with problems connected with the utilization
of new elements or the further development of electronic computers
and their use in the military field and other areas of the national economy.
The 1ntroduction and Ch. I w4~re,.writtcn by Yu. G. Chugayev, Chs. II, IV,
IX and XI by V. A. Plisko, Ch~ III by S. F. Bavarov, Ch. V by A. 1. Kachko,
Ch. VI by A. A. Pashkov, Chs. VII, VIII and X by V. M. Bol'shov, an d
Ch. XII by S. N. Grachev. There are 14 references, all Soviet, including
1 translation from English.
TABLE OF CONTENTS:
Foreword
3
Introduction 5
Historical review. Purpose and field of application of
electronic computers [EC] 5
Card 2 / V ~-

f 'Or'
CIIUGAYF,V, Yuriy GennAdiyevioj PILISKO Valeri ;, RAVAROV, S.F.;
I " _L V = p A.A. I KACRKO, A. I.)
. . .1
IDUISHOV, V.M.1 GRACHE , . jTHKOV, ~A.A.~IKAC
I PLAMNOV, S.A., polkovnik, red,; MZIDNIXOVA, A. If., tekbn. red.
[Electronic digital computers)EIektro-nnyo tairrIow" vychislitoll-
nye mashiny. Moskva, Voenizdat, 1962. 405 P. (MIRA 16:2)
(Electronic digital computers)..

PHASE I BOOK EXPLOITATION SOV/4304
Plisko, Valeriy Antonovich
Elektronnyye mashiny v voyennom dele (The Use of Electronic
Compixters for Military Purposes) Moscow, Voyenlzdat, 1960.
74 p. No. of copies printed not given.
Ed.: S. A. Platonov, Colonel; Tech. Ed.: M. A. Strellnikova.
PURPOSE: This booklet is intended for those who are interested
in the study of compdters and their military uses. Attention
is given to the use of computers in armament systems and for
training purposes. It may also be useful to the general
reader who wishes to acquaint himself with the principles of
electronic computers.
COVEWE: The author describes the purpose of computers,
classifies them according to types, and considers them in
relation to their capabilities in solving military operational-
tactical problems. Several examples of the military use of
computers are given. No personalities are mentioned. There
are 10 references: 7 Soviet and 3 translations from the
Card 1/3

The Use of Electronic Computers (Cont.) SOV/4304
Engl:Lsh.
TABIZ 01? CONTENTS:
Introduebtion, 3
Electronic Machines Which Calculate 5
Types of Electronic Computers 14
~Basic U.Ats of Bleetronic Computers 17
Electronic Machines Which Control Combat Equipment 21
Electrdnic Machines Which "Think" 40.
Pobsible Use of Electronic Machines in Solving Operational-
Tactical Problems 43
Use of Electronic Machines in Military-Scientific Invest-
igations 54
Card 2/3

F
ar': "ovi
Ye
Stepan Dan' loi (Itei~a- N _1 kc.1av--vich Dani 'I c-,r
TITLE.
His 70th Birthda- (K '10-letiyu so dn-- rozhdoniya)
PEELIODICAL: Zhurnal prikladnoY 1,,hinii, 1'1~55, lir 1, -;~P 31-5 (USSR)
ADSTRACT: This is a short ',id-.-Uraphy of Stcp--n 2*ikolayevich Daniiov,
Director of the Institute for Hi'~h-laolecular Compourc?~ of
AS USSR. He W&.3 born on r' January 1261, in Vitebsk and was
-raduated from the PetersburC University in 1914. In 1030
he was selected as Profeusor and Head of the Chair for
Chemical Processing of Cellulose at the Leningrad Techno-
logical Institute imeni Lensovet, and since then he har,
cccupied this position till-to-day. At'present he is Pre-
sident of the Leningrad branch of the Chemical Society ime-i
D.I. Idendeleyev and Corresponding Member of the AS USSR. Ele
Oas awarded with 2 oiders of Lenin, one order of Labor Red
Banner, an order of ~'Sign of Honor" and with medals.
There is I photo.

Y A.; DANILOV, S.N.
PLISKOF
Water-soluble sulfometbyl and sulfoethyl cellulose ethars.
Zhar. prik-1. khim. 36 no.9.-2060-2064 D 163. (MIRA 17:1)
1. Institut vysokomclekulyarnykh soyedineniy AN SSSR.

PLISKO 1, -`;3. -A-.- -1 - - -. -
Inorganls Chemistry
Dissertation: *The Swelling of Qulnine In Electrolytes and 4yntbesle
Iof Its Ethers.* Cand Chem Sci, Inst of High &Aecular GoApounds. Do-
. partment'of Chemical Scie *nces, Acad Sci USSR, Cat-Doe 1953. (Vestnik
. :Akademli Nauk, Mar 54)
SO: SUN 213. 20 Sept 1954

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sivilled -by MOE.

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,.dTMORSI
ftngl
Klenkova, W. I. and Plisko, Ye. A.
79-2-26/58
PIRTODICAI:
ABSTRACTe
Caxd 1/2N
ftdi-cphilic Properties and the Swelling Points of Chitin (Gidrofilinye
avoyetva i Teploty Nabukhaniya, Khitinay
Zburnal Obsbcbey Xhimii,-1957, vol 27, Wo 2, pp. 399-402 (U.S.S.R.)
Fxperiments were conducted to determine the hydropbilic properties and
swelling points of chit'n 010260102) and compare them with analogous
data for cellulose fibers.
Tt was established that the specific heat of chitin is close in magnitude
to that-of cellulose fibers. The moisture absorbed by ebitin at 100%
ta~ a922mlosw ftbersl freezes almost cam-
7-,-Wt"~Lt, 4tb~dt !A tlut fl~"liz-11-M. !IUD: -M-- V--n&Ax~- imrar-.13-r- A-Crix". M---2aC&
A4nv the va-ber- =Det---~r -t--% Aam -,t=
Cleo* *.C, CW!"MICee =rr
tl~&-- rwLto -111tez-3- & studvr of the MWIlln-g paimts af C:141,1~ !M
sod-4.um hydrax-Ade -.!* zf -.!!a frt~a
viul WE a-c-lec-a2es chit!-- is %Z41-te -'Cor-ticat-ed- !-%-

Hydrophilic Properties and the Ekelling %ints of Chitin- -196-0-25/52Z
indicate that the structure of chitin is less accessible to reagents
them the structure of cellulose fibers which lies in direct relationship
with the low.reactivity of chitin di=ing esterification.
Air-dry chitin as well as chitin desiccated at 1050 3-q highly water
abscrbing and calorimetric measurements were possible within several
miniftes.
2 Ubles. There are 5 references, of which 4 are Slavic
ASSOCTATTON3 USS11 Academy of Sciences, Institute of High Molecular Compounds
PRESMM BYt
SYJBKITTRD: March 10, 1956
AVATIABLEs Libmry of Congress
Card 2/2

DANIWV, S.N.; PLISRO, Ye.A.
2qrn, af

'-"~ ~ye A-.
Sjmthesis of cellulose ethers by means of benzenesul-fomtes.
ME% ob. Whiir. 31 no. 2:474-4726 -7 'a. V. =,-I i4:2)
L. Institut vysokomoleku:Lyarnykh soyedineniy AN SSSR.
(Cellulcse) (Benzenesulfonie acid)

A

-ASD
37T2
-A. OPM/0/036/00030/13P7
Te'.- kj t I Abu-
VITISS _-Obtainimit: sinvle fiite,ia asi LtMiXinR AMbutitutee,vith a briLndh*&*,*1
'
on Ch
Cs, b

tBOURCE no 1963t 1303-1367
chai
TWICIAGS4 eirtid, ..Colluloset-C-arbon, ng-Asopropanst- is-obutme tribixtane.-

-been shown that previcrusly-described W*nown iso ropsn
_p e. so-
'
-and tribe
tsue esters-of the,benzoloulphurio acidi alkaazing -media.
iThe- films fromt1butans isopr6pane,esters of cellutose.posseas high mechanical

PrOpe iese. artelbass 6'tibleso-
rt

Aq4W=wi nixtitut, Ai-, SSSR.
qj*~~w 4M. Mal

Swv
M=2

XOZWV, H.F,7; KOZINBA, O.P.; PLISKO, Yek, A. DAN-ILUV, S.N.
I-------------------
Meclumism of oxidati= aff cellulose others by pArt. 25; Effecz
of the chain length of the substituent in aliphatic celln-lose ethers .
on their oxidation rate. VysokQmsoed. 5 no.3:424~427 Mr 163.
(NI-RA 16:3)
1. Institut vysokomolekulyarnykh soyedineniy AN SSSIR.
(Cellulose others) (Oxidation) (Substitution (Uhemiotry))

ANIKHYXVA.
SteVLn Nikol"vich Danilov; on his seventieth birthdily. Zhur.
PrM.:.khis. 32 no.1:3.-5 Ja '59. (KMA 32-: 4)
Mailov. Stap&A Nik-olmavich. IWIS-)

PLISED, Te.A *
Sea:.,ch for now synthesis of cellulose ethers. Zhur.ob.khimo 28
no.:L2:3214-3216 D 158. WRA 12!2)
1. Institut vysokomolWmly&Mkh soyedinenly AN SSSRO
(cellulose)

I PLISKO. Ye.h.; OKUKI, M.G.; GRAD, N.M.; GINTSE. N.F.
Work of S.M. Daniloy in the field of cellulose and Ito others and
asters* Zhursobe)thime 28 no-12:3174-3184 D '58- (MM. 12:2)
(Danilov, Stepan Nikolaevich. 1889-)
(cellulose)

i~THORS: Danilov, S. Ye. A. SOV79-28-8-45166
TITLE: Investigation of CMin (Izucheniye khitina) Ill. Hy-droxy-Ethyl-
and Eth I Ether of Chitin (Oksietilovyye i etilovyye efiry
khitinZ
PERIODICAL: Zhurnal obshchey khimii, 1958, Vol. 28, lir 8,
pp. 2217 - 2223 (USSR)
ABSTRACT: The authors had previously pointed out that the synthesis
of chitin ether is made difficult by the fact that chitin
is swelling very little in the solutions of alkali (Ref 1).
The investigation of the heats of swelling (Ref 2) in solutions
of sodium hydroxide shows that the reaction of chitin is
inhibited by the lye. In former attempts to attain the
hydroxy-ethyl ethers of chitin it was found that these are
not formed under the same conditions as in the synthesis
of the hydroxy-ethyl ethers of cellulose. The etherification-
and activation conditions -with alkali liquor were varied:
chitin was treated with alkali during freezing, the etheri-
fication was carried out at higher temperature which took more
time. Besides, the chitin was used in theetherification
Card 1/3 in various states of pulverization whereat the molecular

Investigation of Chitin. 111. Hydroxy-Ethyl- and SOV/79-28-8-45/66
Ethyl Ether of Chiti~.
ratio between it and the ethyleneoxide was also varied.
Hydroxy-othyl others of a high degree etherification were
obtained which are soluble in water and diluted sodium
hydroxide. The ethylation of the chitin treated with alkali
liquor was performed with ethyl chloride in sealed tubes
in the autoclave. The newly synthesized ethyl-ethers of
chitin are soluble in alcohols, ketones, hydrocarbons and
eaters. The films from 'ethyl chitin are equal to those from
ethyl cellulose as far as their durability is concerned.
There are 3 figures, 4 tables, and 7 references, 5 of which
are Soviet.
ASSOCIATICN: Institut vysokomolekulyarnykh soyedineniy Akademii nauk SSSR
(Institute of HighwMolecular Compounds, AS USSR)
SUBMITTED: July 4, 195T
Card 2/3

Investigation of Chitin.
Ethyl Etherof Chitin
Hydroxy-Sthyl-,and
SOV/79-28-8-45/66

AUTHOR: Plisko, Ye. A. SOV/7~-28-12-10/41
TITLE: Search for New Ways of Synthesizing Cellulose Ethers
(Izyskaniye novykh putey sinteza prostykh efirov tsellyulozy)
PERIODICALs Zhurnal obshchey khimii, 19r;AJ, Vol 28, Nr 12, PP 3214-3216
(USSR)
ABSTRAM The synthesis of low-substituted methyl and ethyl ethers of
cellulose by means of dialkyl sulfates is troublesome, not to
mention their harmful character. It was, therefore, of interest
to find new alkylation agents for cellulose. The methyl and
ethyl eaters of the p-toluenesulfonic acid were used as alky-
lation agents besides in other compounds (Refs 1-3), also for
cellulose, yet the properties of the ethers obtained were not
described (Ref 4). in the present paper the alkylation of
cellulose was carried out with p-toluene sulfates as well as
with toluene-di, benzene- and o(..naphthaleno sulfates accord-
ing to the scheme:
RS020R, , (C 6H1O0 On --'[C6H,O_X' 5-x (ORJ)xl n, where
R-C6H 59 CH3C6H 59 C10H7R,=CH 3'C2E5'n'-C3H7n. _C4H9'C6H5
Card 1/3

Search for New Ways of Synthesizing Cellulose SOV79-28-12-10/41
Ethers
Alkali cellulose, a cellulose dissolved in triethyl benzyl-
ammonium hydroxide, and a hydrocellulose dissolved in a 9-10%
i3oda lye were alkylated. The alkylation of alkali cellulo *se
failed. The alkylation of cellulose in the solution of an
organic base takes place more intensely than in an alkali
iiolutiong with even in the latter case only 3-10% methyl or
othyl radicals being introduced, as compared to the 12-35% in
i;he former case. In the alkylation of the cellulose dissolved
in alkali liquor with benzene sulfates the methyl eater reacts
more readily than the ethyl ester, and the latter more readily
than propyl ester etc., which, however, is not the case when
using a cellulose dissolved in an organic bass, as that reac-
tion takes place more intensely. For details see experimental
par'.. There are 2 tables and 5 references, 2 of which are
Soviet.
ASSOCIATIONt lnstitut -.rysokomolekulyarnykh soyedineniy Akademii nauk SSSR
(Institute of High-Molecular Compounds, Academy of Sciences,
USSR)
Card 213

AUTHORS: TplijLko, Ye~ A., Okun', M. G., SOV/79-28 12-3/41
Grad, N. M-.-,-Tintse, 11. F.
TITLE: On S. It. Danilov's Work ir. the Field of Cellulose and Its
Ethers (0 rabotakh S. N. Danilova v oblasti tsellyulozy i
yeye efirov)
PERIODICAL: Zhurnal obahchey khimii, 1959, Vol 28, Nr 12,
Pp 3174-3184 (USSR)
ABSTRACT: The manifold, scientific activity of Danilov was closely
,onnected with the chemistry of cellulose and its derivatives,
-as well as with alginio acid and chitin. It led to new findings
on the behavior of cellulose to its solvents, on nitrocellulose,
acetyl collulose, nitro-acetyl cellulose, cellulose ether, the
hydrolysis of alginic acid., and chitin. Together with GintseN.F.
Danilov investigated the solution conditions of cellulose in
:?hosphoric aci.d (Ref 104), and it was found that the hydrates
;?lay an important role in their dissolution in concentrated
nolutions of the electrolytes. A new method for the
determination of the copper numbers required for im-portant
outstanding properties of cellulose (Ref 67) was devised. The
-ation of the cellulose molecules with one oxygen less,
Card 1/3 nvestiC.

On S. N. Danilov's Work in the Field of Cellulose SOV/79-28-12-3/41
and Its Ethers
.thei_r desoxy, anhydride and unsaturated derivatives raised
Irreat interest. The use of acetyl cellulose membranes as a
substitute of glass in hotbeds was worked out. Danilov's
excellent investigation of the nitration of cellulose was
proof of the nitration theory devised by Mendeleyev-Sapozhn:kov
(Ref 68). The oxy-butyl ethers of cellulose (Ref 51) and the
Varboxy-metbyl cellulose (Ref 35) were synthesized for the
ftrst timq. The work carried out by Danilov and his cooperators
on chitin considerably widened the knowledge of natural polyme3s.
114-9 work in the field of cellulose ether and cellulose ester
is directly oontinued by his viork on cupravimonia solutions of
cellulose, xanthateB, and vis,2ose. The cuprammonia solution
cif cellulose consistp, according to Danilov,, of the high.-
molecular compound: f(C01005 )x - [Cu(NH3)M(011)2]y . (H2 0) J n'
mhere the cellulose and the cuprammonia base form a molecular
compound of variable compositon at the expense of the hydrogen
Card 2/3

On S. N. Danilov's Work in the Field of Cellulose SOV/79-28-12-3/41
and Its Ethers
bonds. The viscose research was widened by new knowledge
and was put on a new basis (its compositon during the process
of maturation). In Danilov's laboratory synthesis methods
were devised which are closely connected with the technology
of viscose processing. There are 141 referenoes, 130 of which
are Soviet.
Card 3/3

DAHILOV. $0L.;PLISKO, Ye.A.
.Study of chitin. Part 3: Oxyethyl and ethyl chitine others, Zhur.
ob. kh1m. 28 no. 8t2217-2223 Ag 158. (KIRA 11:100)
1. Institut vysokomolokalyarnykh soyedinaniy AN SSSR.
(Chitin)

himmommumma~
S K, C,
DANIWV, S.N,; Plaw. TO.A.
-Study of chitin. P*rt 29 Glycerination of ehitin ethers. Zhtw.ob.
khiu.2:4 no.11:2M-2M 1 154. OffJIA 8:3)
1. Institut vyookosolokulyarnykh soyedinenty Akadeviii nauk SSSR.
(Chitin) (Glycerol)

14-,
KI&MOVA,
H.I.; PLISKO, Ye.A.
vwmm- -- MallmOt
t,drophilic properties and heat of swelling of chitin. Zhur. Ob.
Idilm, V-no,2099-402 7 157- (MMA 10:6)
1. Institut vysokomolekulyarnykh soyedineniy Almdemii nauk SSSR.
(Chitin)

PLIS D, PYAIVINEN., E.A.
umwv, S.R
Ethers end the reactiTity of cellulose and chit4n. Izv.
AN SSSR. Otd.khim.nauk no.8:1500-1506 Ag 161. (MM 14:8)
1. Inel-itut, vyisokomo3.ekulyarnykh soye4i~eniy AV SSSR.
(Cellulose ethers)
(Chitirl)

PLISKO.Yu.. inshener-mayor puti i stroitelletva
Using ca:Ae cranes at railroad coal depots.
86-87 047.
(Cranes, derricks, ate.)
Zhel.dor.transp. mo.10:
(mm 8:1z)

L 04682-67 EWT(d)/04T(m)/E.WP(V)/T/EWP(L)/ETI/LVP(k)/-VWP(h)/EWP(I-) 1JP(c) JD
ACC NRs AR6020937
SOURCE CODE: UR/0137/66/000/002/BOIS/BO18
AUTHOR: P1pko, A. L.; Pliskovskiy, V. Ta.; Puzyriyakiy, Yu. S. 119-
TITLE.- Component transfer mechanisms in vacuum and hydrogen resistance furnace@
~
ISOURM: Ref. sh. Nctallurg, Abs. 2DI20
IREF SOURCE: Elektmtermlya. Nauchno-tekhn. sb., vyp. 45, 1965, 17-21
ITOPIC TAGS: vacuum furnace, resistance furnace
TRANSLATION: A description of several types of a transfer mechanism for components is
presented, the tr4.w fo:r mechanism being one of the basic units of continuous vacuum an
Oydrogen resistance furnaces. In particular, a schematic the "walking beam" trans-
fei mechanism used in the LM-4460 continuous vacuum furnacNa described and charac-
teriatics of this t)pe of transfer mechanism are enumerated. It was demonstrated that
this transfer sechavism may be used with minimum Ma . t ce in vacuum furmaces with
different standard ilimensions. The construction o tr=fer mechanism units, design-
t
ed for operation uniAr ultrahixh vacuum conditionsk a described (the vacuum in the ope
8
rating zone of the furnace u1-10-9 = Mg). 6 figures, 5 references. V. Pryanikova.
SUB CODE: 13 It
Heat tzeatizg\
Ev.
UDC: 669:621.783:621.365.4

--~~14K,~g,-Il~~,-,�i~i~lkand.tekhn.nauk; SUCHKOV, Yu.S., inzh.
Measuring raean values of stresses with sire and vibration-
frequency pickups in the prenence of vibrations. Priborostroenie
ito.11:8-10 N 165. (MIRA 18:12)

AKINOT, N-1-4 TOLOT, S.P.; KONOTALOYA, N.A.; OSINOTGUTA, R.I.;-IF-LI-3XO,
,,.TUjU--q,*-_~qT=O. N.M.; SWANOT, L.A.; SHCMXINIC'T.Ta.; TOROVi'--'-
M.P., red.; TSARXHKO, A.P.. red.; VMXA, ';G.P.. takhn.red.
[Intemational railroad transportation) Mozhdunaroduye thelesno-
doroshnys soobehohnniia. Pod red. X.P.Toronichave, Koskva, Goo.
tranap.shol-dor.izd-vo, 1959. 242 p. (MIRA 13-.2)
(Railroads)
~dm-

PLISKO, Zoya,-4~,
The dearest of all. R&dA sial. 33 no.12:19-20 D 157. (MM 10:12)
(Miziek-;-Courts)
(Women as judges)

PLISKOHOS, K.
I.-I.-
Metal. in exceso of the plan. Sov.profsoiusy 7 no.1:43
Ja 16o. OGRA 12:12)
1. Predeedat.ell komiteta profsayuza Magnitogorskogo metallurgicho-
skxgo kombinata.
(Magnitoggrek-Steol industry) (Socialist competition)

PLISKOVA Marta inz.; HAMATOVA, Eva, inz. dr.,, ScG.
Effect of mulching on the development of microflora. Rost
vyroba 9 no.5:501-510 163.
1. Ustredni vyzkumny ustav rostlinne v-yroby, mikrobiologicke
Oddelani, Rizynei*

PLISKOVSKAU, L.K., poapolkovnik meditsinakoy BluzhbY
Features of the clinical course of diffuse nephritis. Voen-med.
zhur. no.lOrl4-18 0 '59. (MM 13:3)
(IN ITIS)

L 04o6o-67
ACC NR- Ap6027433 SOURCE CODE: UR/0125/66/000/007/0060/0062
AUTHOR: Yermolayev, A. P. (Moscow); Zlatkis, I. V"(Moscow); Pipko,
A. J. ()163001w); P:Lisko_v$kL7_,,_,Y- Ya-. (Moscow); PuzV63rokly, Yu.' S. Imose
!
T3y5U_'1'skIy,v I. V-71moscow)
ORG: none, . I zh~_
~TITLE: Following mechanism for arc welding In an inert gas
CE: Avtomatiabeskaya 9varka, no* 7, 1966, 60-62
C TAGS: are irelding, inert gas welding, feed mechanism
TRACT: The article describes the construction-details of s'new type
loving machanium said to assure stability of the geometric dimensions
the welding seum in welding In Inert gases with high ionization
entials (for example, helium), (See Fig. 1)

L oho6o-67
ACC NRS AP6027433
Figure 1.
~Construction of
following meebanism
~a--in position for
4welding seams on a
cylindrical surface
*b--tbe sane for an
and surface.
A2
,vA
13,

L q4o6c_t-6T_____
ACC NR: AP6027433 10
'Electrode I is fastened to support 13 by means of clamps 2, 3, and 4,
Clamp 2 makes it possible to rotate the electrode in a vertical-plane
and to change Its position from the horizontal (Fig. 10 a) to the
vertical (Fig .I,, b). Clamps 3 and 4 make It possible to regulate,
respectively, the vertical end horizontal positions of the electrode.
,The support is connected by 9 swivel joint with lovers 12 and 59 which
are connected botween themselves by link 11. Lover 5, with the aid of
link 6 and lever 7. is connected in a swivelling fashion with abaft 9"
.which can execute forward and backward displacements, activated by a
-Type MP-100M of SL~-161 electric motor,, 10,, with a built-in reducers
Experimental teuts of the mechanism in argon are welding have shown
reliable maintenance of an interelectrode gap of 1 nm, with an accuracy
of � 10,'vf, in a 37ange of welding currents from 15 to 150 anps, The
article-also gives'a detailed diagram of the electric control circuit*
Orig. art* has: 2 figures.
I
SP CODE: 13/ SUBM DATE:
O2Mar66/ ORIG REF:' 004

Its V
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P. Concludirs: (1) #- and #-O*NC4II4Me anti Knott of their dwfivq. give with ak. Z111111 0
Alkafirl Ifilwilli-I CovillidA. (21) anti lit drrivs. do not forin dibentyl
ts~ (3) The --halogru livrivv. (Side Chaill) ill I, and p Ilitrin,4411. fir- at., fonn too
=
-Ulc. x4oll ethm as bY-pmhICt,,l. while tile w derivs. give v%ClU,ivVlv rt)[Cm -.00
(4) * The unstAllk- intermardiatc reacticat profucts itt the lf~nmtim Ill the dil,,,nYv6
cannot lie 6ohitewl. 01) Otily o- and p uitnitoluenvs and their deFivs. it, whirl, jhr
Ito ptillp tw tile Ilk. mUlue call enter file plItitims AdjAcrot to-tile -tnulnw~ric- If
(traliblxm"l from the mitle chain) cmi foini thlicurvi cottilmlo. (oil All
still Knott tat their derivs. react in tile tAutottleric tate, foraling Undcr thr action got MIC. 0
A me I ALI N&0111 unlitable malts of quinuid character. (.) Ths- ItIVIVIAtion -4 StillMI&V too
tab" place thrm4b the intertmediste staile of NO c~mjxl%, (M) At elryatcd tumps,
the action tit sle. alkalies may procectl without the lomation of stillwnel. polisibly boo
omplis. cr-Ill -- I --- L - 00
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fivimilm, tol 11". 10~111111#m okhm
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Obl' "list. bY C~X. is w" -It Ilv vvitit. with ello".
A. A. P-liffingto;

~Jdl

'00

j A I a . I L 41TALLUMKAL Liftn&'?Cgt CLASSIPICATION
M_
iil~t
u u It
to to It it at F it of a PC it
0 0 0 0 do~ 0 0 do do 0 0 0 0 do
W 0 41 6~04 lee
0 0 0 0 0;10 0 0 0 0 6 0 0 0 a 0 411 0 0 0 0 :
06
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Of
4 4 a A:Wjl Uli MA my-mj-v .1 11 At 4 wk-f"fy
I
I I I T -11 V 0 X r Ix PP. LL~1. A.. t-" a J- I-
to
00 A
Mean 11hely 001 JINCh pracle In site marne way as the N -00
codditis. The metallic ollmlem AM give onlime asks i-
A~ Mbw. 00
**a S. 4.) 4. um) 14o M) I d A. A which theis kw mietal still N. kivirill 9. With NaNOo flit
(1) Von to 114"d. by flit wive .1 N(). field at I is smaller Immune al a Pr'"Mulmly Ammitint, 44 00
*0 N(Aft N IlNOi, Ila N44, Cu(NO.), as N&NO, pis the 11 'he &&Ali produml. Ilratin 11 with 14,0, C111)
*0 ascessid,24(n Tte#s intiltiodo yitM Vatted. Pollos. of aillialmnled"ttil
juive flit use of large Vo6. of solvent. W the products sic 1. Nil. suit N. At
I and do wat 1;11 ZINO. At 140
009 Tm tomwtwn of I Inv a U " HNO. is Im"bly " due 176" AvOll and WIrCN pttdontinate. U (2-5 s.) still IW
to by"Ysis &:am tho raw" ukw wild Wilk cc. RID with 1.5 millm. NO tlt;mi N*N(I.. FcM, and
litalmlemadmit. whereas Ilso lsydrolyz.", Btu Iiiii NHOII IIIS0.) gave Is it. 1 (931".J. ~-r frarthm Illint. after
by 11169" proceeds s3orly mod does pft so to completiom. standing I day wassaid, with Ns,,SA).mW thisillsid. until, =00
000 Tin = the distillate no lormer gave a brown color oulently wanti-i
,;msof N., M0 and NO in ~* nFeection
Vm lite following mKkkm N rt ing with com . N&OH. The upper layer of I in the re- Ville
I N
MVtr Wag anid., the &q. kyw esta. with N`aCj atki the =
004 NO + AcC(:N0DIF-NIs (M). 13 NO - M + 00
99" HP + N 0 + 2Aq. It distri. repeated. This proce wall r"Cated. Nor (from z
for-rd In good Of
yi" is either 1100 in l(tio WAS.. t iddis. CuINCh)# and free Irm 0#) similarly save 4 1 Tv 4A 1 (it,
14 =4 11.6) owl 44% (In HIP). Cimilblit **a ."llelitur'k ir, a 0
11111,110 a 'Its"
U" Ilk CIMOWICC~ 114hiend OVAI 1111, W (A. 346
(IM)) found that 11 and IINO, gave wc(;~OM)15. wd,rd to keep thr ",Wfkln Itillf. at (IN-Ill frillp NO).
mod AcOH. but P. did not obwrvv Ohm products, I Was t(roul IINU, mid A%O.) with 25 a. U and W -70 cc. 110)
prbdw P"-. Siam a definite,quantity of HNO. grM%oll. Themixt.waactioledatibel i i to
bill
I in'. D (26 84. W-W cc. 11.0 and 30
since M Is lomtd It is doubtful uWber 7Mh
18
(d. 135) gave. after 2-1 firm. reaction. flol,' of 1. A
ni=yz to I by IINOi as postulated by Cho" I ( !agle
comed. &q. ado. at 82 s. IISNC~ was mixed with W g. U
"ad. ", 1416 1878) j 1 M2)-, so 1053
and hictsio (~. pwdlo. Chm. 121.30. 37(19W). In water. Warming un the 11,0 both (with couling it t4t
I'Mocilm limentit violent) until the evolution cif saws
103); SS, liki(1897). So. It Is I
L
an I dWa, as in previous
4 S. C110:0.11 still
- (25 jr.) and 24 x. N&NLh tjoill
A J.JLjJ.LVf:(.KAI jjff4&jjPj (tA%Jjf1CAIJ0*, Lewis W, puts
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0#6 -0 4244 .4, Oki
I g 1~ - --W ' . W-1-
it x W IN 2 di a V
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oleo #1 as 6 0 6 1)** 0 0 0 di 9_0 Ill 0 111 0 0 Ili a a a OA

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0 P-dUct is Obtained. A 2nd od&Um ot the UwAidil., too
P-1 -4 U- ad Silms b-W muft, tMn tM 1,t
M. Lckvstr
reo
Do
too
of ALtUROCAL LITER610C CLMSOKATIOP
slaw
unoill-L Iola*j .4v 04. oat 1111111cwti &I,
go , - I-, ~j F I I --5~, -jF 14 0 ila3 1
"I; ~ 0 a 1; 0 a a in 19 v Ilan I(OlKwn I!"
0000100009 000 00 000000 0 0 Co 0 0 0 0 0 0 a 0 0 0 0 00 0 0;
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Ir v
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-00
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C". (1). S. S. It.) 0. M 14 -00
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4 gam lids i4 4k. -00
00 with %r/0 ykm by UILWIllm 4
Me Kr. of 4,wboxyug "ilk a" Ow SAYACkt, so*
so im bewd oa the jamij. of the Wtcv it, PtuOklml cttwc-
Oita, Gfbr amtralising and =00
NI.Tkup gluk ps -1. d- 1% Ca vmothcwt~ 0% a
vpab-~. was antzed witb 0-' 0
QvAjywj. and thm wom "allummi vith sit LcomWills I
RJR 0 22 mam. in zoo
00 ow Willi. th"Mak a ab- tww (4 w. Ism
"o.) twisted ekctsk*97 at Ils-W% Ilse vemtko
d , &. with no% Naoll mid freed f"= Leo
product in
for 5 "do. Tbt alk. solo..
VACINSUP11 ad by maUituffiN
fived from say mumpowifistak Matter with peudrut"
-us. 11W alty"S
lkt%mpd. to pep. Sill, ft
w .41 by Sh4k, with Coo
film t1w rallmlytiC A. ills
Ch". IIIAIW
.4fALLUftGKAL LIURATLAtt CLASSIFKATION too
Np~;, 'S
41--En,!~ a.,
U 41 so &1 0 fm a' I w lit
t# It OF N a A It a I( If If W ft f~ 14
0 0 0 a 0 9 a 0 0 0 : : : 0 U 0 0
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2
tkOn the ProPertios of Peroclides in oxidized Parafilrin,it Zl~u.-. Cbshcn. 9,
1939. Uborat-cry of Organic GherliStrY, Krasno-d-arsk GhcmJ-co-Technolor;lTiCelj lm;titate
. Received 25 May 1933.
of the Fat Jndus*~ry imeni Molotov
Report U-1517, 22 Oct 1951

PLISOV, A. L, GRMPNNIKOVA, 14. D.
*Wdation of Petrdleum Products at High Temperatures
Oxidation of Solar Oil,,"
Zhur. Obsheb. Khim., 9, No. 6.. 1939.
Laboratory of Orgamic Chemistry, Chemico-Technological
Institute, Krasnodar.
Received 14 JulY 1938.
Report U-1517,, 22 Oct 1951

Al* vooplailts P-0tv

~
wt
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AT
6A Cb
v. ommanymm
mad throw& saw
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ot Wow'.
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MA rim a
at Wimp. >60'. IAC T.
eon
A
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a 41 dl a 11-a-d-11W
I
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t-
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es
see
1200
too
-ve,
too
AV 10 4% AM I s 9 ew 0 ON 4 1 W IN
4nc
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a
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to - ------ VLI.A~ Ula

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so
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see

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abow r1*14111110 a so
iu/ id"as -s T- fellaw a.. Got WIC &v dwv &$I
INA is - AV - ft P JIM a 9 A 6 3 1 T

1
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PLISOV, A. K.
20554 ILISOV, A. K. 0 sposobe rolucheniya elaidinovoy ki-sloty. Trudy krashodarsk.
in-ta yishch Frori-sti, vyp. 4, 1~48, S. 51-55.
SO: LETOPIS ZHMNAL STATEY - Vol. 28, P-oskva - 1949

ILISOV, A.K.
20553 FLISCV, A. K. 01,staliticheskom pazlo~,henii kislot I Inyanogo r.-f-sla. Trudy
krbsbodnru~. In-ta n:'Lshch. lrom-.-U, vyIr. 4t 1W, fl. 111-13
SO: LETOPIS ZHUFd4AI- STATEY - Vol. 28, Moskva, 1949

PLISOV, A. K.
20816. Plisov, A. X. Okisleniye rastiteltnyk-h masel pri vysekikh temperaturaj~j.
Okisleniye masel perilly, konopli i 11na. Trudy Krasnodarsk. in-ta pishch. prom-sti,
vYP* 1+9 1948t so 115-2-2.
SO: LETOPIS ZHURNALSTATEY - Vol. 28, Moskva, 1949.

olldatinn and dabidtation ol ca"w ad. A. K Murv
AIM 1-'. C.. Toospu JO&iiss Canning
Amp. 1'rikl4d. Xhim. (J. Applied Chem.) 23.
()W).--A wrivii of oil-I*. to ptcdiscr a dryins oil on dr-
hydration 44 CA-tor oil by 1..Wnwafqt 1-4"W 01 the I&Itrr
at I rul./min, throogh a vert" At tube (1-2 cm. X 101?
CM.) heated over M cm. lenitils by an electric furnace
othrovetl Out Ow following optimism coiWitions D"Ild he
jj~d %hen Nk 411 S, artivalc4l clay filter in inint: 411W
Jobe to,ols. 411.1 sit 6441 to (At of .1111,
1, 'hi. Me Iwisluct under Ihr-w coodiljoiss rrimlily lorm%
a tough. clear colcwle~ film on drying in air. and addn%,
of 0.16r, Nfn(h and 0.0% PhO sciviewhat accelerate the
ilrying proc".. G. M. Kcw4almff

A -7
CA
0ZWJltM Of pdfaPft-. A. J- Pltov
"id. A:kim. (J. Applied Cloven.) 23, 12--9
W&.*.fw).__Pjr,it1m. pulloord intnan Al tailor lie -t curTrilt of ail
milh tittle of Altoopme, I one". at _144)-5f a I% was olkiffic"I
too n1i%"l InNI11vto, ill 4A.1rer let expl,wr lite rem-liull irl the,
Inglitir-trinp. tanigm thitimum voluiliti(mo% .4m. it-lilp.
4111k.1%,41 3401 4441'. - hiselter tirtlep. yield, I'.. muh Col..
..0 11 ... l I.A- 1. fit., .4jill ni.sloW fl,)%% I ml.jinin. A
1114"r UApW aur fit'. givir, J.Koer timircertioll'. The Pruilint
1.1 thm nblannif toy liziel'iti(on few Inany bl,. at
I... %rf front, I It.- prn,hui i~ Am..,t f,": ..( hy.hpiry no W-
.On-1-141mu- A-h-hyd- (1-t. 64 mg. Aril tvah,l. I feel I X.
41111%Ulft'd I-At.01-10 .111-1 At'. Ilk-A, 1.1611 Ollie. Mril)lj (calvd.,
tw. lie 2.4 mul'.1 1-1 t%,lnliliml~.
G. M. K11,411.1loull

.Z 4-
P. ~
v
; ~!VAS OIPWUyMIW,*,,t @MUM" Tf=~4~-
'ApPi'd CI... U.S.S. , (0,
R. U. 13sl-wlvwxK"gl. tmn$6-
tion). Sec C-4. 46. AWAId. a. k.

ptisovp A.K.
1
11
-~
C I id. A. K.
m- and H. G. MaleLvu
I
1: " 0 111C ac
4

c" at. VIT M
, ~.., . Zhur. naKmm -P-r
4
7
--(I (h., 213-13.5-, (11, 0,8790, ill
ale. K011 was exallid.at 2Y tli,-, reaction la-ing followed by
deln. of clerti-moad. rjf tfi~reaetioa inixt.; tioder identical
CL. .& conditions Mcdaillalt, 1,i, 21-l', ill. 0.87111), was id5l, !,11mlid,
with ill(:. KOH. 'I'll,: it-milt% giv'ell ill of miative
chaligm "I collul. lildivatc that Ale claidate "4(pollific:; more
rilpidly Own lilt: oleate. of thi, c,~turs ovi-r.
Pt-MISO, ill Moll Showed that tile rate of hythogellatioll
of tile claidate is smallcr than that of the uleatc hv a 1: 1.14
factor; the free acids show a imil~~r ratio (I : 1.15). Oxida-
tioli by aq. KNI110. follm%erj :;nJactinictrivally shows that
id
idi
ifi
l
d i
M
l
I
h
id
A
y mt,re
mt
a
le ac
an
ts
e emer ox
ze
cant
c
gn
slowly tban the corn-spuadinp oleic. acid all(] its Nl~ ester.
The rcstflt-s confirm tile cis structure of oleic and traus struc-
tore of Claidic acids. G. M. )~osulapoff

Pnsov~ A. K.
Reactivity of &trostdinic and 2 d their
-in([ A. 11 14 411 -ST, 11 1 -
MM
eaters A. K. Illisov. YZ not.
2 US Mega Teri,
P(W-ft Uhsnrn=him. ZJ,
013-1509-rl); cf. C,I. 48, 573r,-Iletroselinic acid and its i
Me, Pr, wid IlliC.111, t~tcrii widergo oxidation with aq.
Kif%04 at 26-55* Ulld ImIrugcnatimi over Pt-BaS04 it 2,3*
Sigilificuldly 11101E. ralsidly than (to pulroselaidic acid mid its
corresponding Liters. - The rale of hydrolysis of the petro-
t:eliuic acid cster.4 by niv. I"Oll, howevur, is smaller thall-
that of the correspomlitig purosclaidateq. These results
fildicute that 1"F(~clillic acid is it Cis Isomer, While petro-
gelaldic acid is the tratis isomer. The esters.were prcpd
the R011 and t-ke dc~irctl acid iii the presence of II-SO4
Alkyl 1,elraseJimules. -Ale, 1)2-3 1584t0'; Pr, b- j 108-2()00
PhUll, 14 218', do 0.9315, x-,- 1.4M. Pdroselaidates
Ale, lh-. III"% Pr, I)_. 200% PhCfl,, b,-s 9"'0 d
0.0372, n7l 1.4812.
G. hl, Ko!

FLISOV, A.K. ; ZHUIRAVLEVA, i.M.
,_--l.__-.-, -!~~ - -. ,
GonfJguration and prcDerTies of acidE 'chef
.. _r -- ---.
Part 15: Synthesis and proportion -bromocinnamic acids and
their esters. Zhur. ob. khir.. 34 no.cl:3102-3107 S 164. (MMA 17:11j

PLISOV,A.K.; BYKOVETS.A.I.
, -.n, ~f
Configu-ration and properties of unenturated acids. Part 3. Re-
activity of 0- [OC-furyl)-scrylic acids and their eaters. Zhur.ob.
25 no.6:1194-1199 Je '55. (MLRA 8:12)
1. Odesukiy institut piabehevoy i kholodillnoy promyshlennoett
(Furannerylic acid)

PLISOV, A.I..; XOSTYUK, A.F.
Configuration and propertios of unsaturated acids ozd of their do-
AT&tiTO8. Part 5. Properties of angelic and tiglic acids and of
their esterp. Zhur.ob.khim. 26 no-3:715-719 Ur 156. (KLU 9:8)
1. (Ideaskly gosudarstyeaW UlklTersitet.
(Angelic acid) (Tiglic acid)

AUTHM: Plinov, A. K., and Bogatskiy, A. V. 79-2-18/58
TITLE: Configuration and Properties of Unsaturated Acids and their Derivatives
Part 6. Reactivity of Stereoisomeric Crotonic Acids and Their Esters.
(KOITFIGURATSIYA i svoyetva nepredellmykh kielot i ikh proizvodnykh. VI.
0 reaktalonnoy aposobnosti stereolzomerpykh krotonovy" kislot I ikh
efirov)
MIODICALt Zhurnal Obabehey KbWi, 1957, vol 27, No 2v pp. 360-364 (U.S.S.R)
ABSTRAM The authors synthesized butyl, isobuty2, isonq1 and benzyl others of
Isocrotonle acid and benzyl ether of crotonic acid and described their
properties.' Crotanic acid vith a melting point of 720 (trans-ismer)
hydrogenates much slaver than isoarotonic acid vith a melting point
of UO (cis-isomer). The authors established the differewce in the relati
rates of hydrogenation of crotonic snd isocrotonic acids; isocrotonic acid
attracts hydrogen very easily. It is explained that the difference in the
relative rates of hydrogenation exist also during reactions with different
catalystw(pt., pd) in different solutions (alcohol, acetic acid) and at
Mud 1/2 different temperatures. It vas found that the increase in alcohol radi-
cal in the enter group leads to a reduction in the relative rate of

79-2-18/58
Configuration and Properties of Unsaturated Acids and Their Derivatives
Part 6.
hydrogen addition and the difference becomes more noticeable when
compared with different crotonic acid eaters.
The trans- and cis- structures of the isocrotonic and crotonic acids
and their esters were established on the basis of the differences In
tho relative rate of hydrogenation.
6 tables. There are 17 references, of which 8 are Slavic.
ASSOCIATIONs Odessa State Univeisity
PRESINM BYs
SUOUTTEN Tobruary 28, 1956
AVATLAZX# Library of Congress
Card 2/2

PLT SOV, - -~.Y.; 15HPANOVA, C,10.
;~ ~ :,.
1-- 1
Oxidatilr,n of a----7 cc.~yl Nauch. ez-'-:sgc;.d, ni-imm.
fO. -0,q. un. nc.---t99-lC2 161. f ~,, rRt
I I . l7s 8)

PLISOV A K - BOGATSKAYA Z. D.[Bohatolka, Z. D.]; SBEYKO, L. D.
I =#- -a J. .9
Vapor-pbase refining of cracked and straight-run gasolines by
means of the Odessa gray-green clay. Kbim. prom,(Ukr.l no.l!
89-90 Ja-Mr 162. (MIRA 15:10)
1. Odesekiy gosudarstv'ennyy universitat im. Mechnikova.
(Gasoline)' (Glay) ~Sulfur "Compounds)
1 0

PIJSCIV --BOGATSKIr, A.V.
Configuration and properties of unsaturated acids and their
derivatives. Part 14: Properties of esters of cis- and trans-
petroselinic acids. Zhur.ob.khim. 31 m.10:3324-3326 0 161.
(MMA 14: 10)
1. Odasakiy tekhnologicheskiy irwtitut nishchevoy i kholodillnoy
pr(aphlenwati i Odeeskiy gomwAaretwom" universitst imeni
I.)..Mechnikova.
(Fetroselinic acid)

PLISOV, A,K.,, BOGATSKIY, A.V.; MOMS, A.I.; BOGATSKkYA. Z.D.
WAtlissis of new sulfamide coupounds. Trudy 01-PInW 9 no.2:97-100
159. (MIU 13-9)
(Sulfamide)

PLISOV. A.K.:,, ZHILA, L.A.
Configuration and properties of unsaturated acids and their
derivatives. Part 10: Thlocyanation of olelc and elaidic acids
and their eaters. Zhur.ob.kbim. 29 no-1:323-328 Ja 159.
(MIlk 12:4)
1. Odesskiy Institut pisbehevoy I kholodil ,noy pronyahlennosti.
(Ilaidic acid) (Olelc acid) (Thlocyanation)

-AUTHORS: Plisov, A. K*-j Bykovets, A. I* SOV/156-5~~-3-35/52
TITLE: The Thiocyanation of Oleic and Blaidic Acids and Their '-;sters
(Rodanirovaniye oleinoAroy i elaidinovoy kislot i ikh efirov)
r
?'ERIODICAL: Nauchnyye doklad,,, vysshey shkoly, Khimiya i khimicheskaya
tekhnolofziya, 1913, Nr 3t PP- 540-541 (Uc'SR)
.j -
ABSTRACT: Thiocyanate solutions are used for the quantitative analysis
of fatty acid mixtures. It was founi that the rate of thio-
cyanation of oleic and elaidic acid in different. The thio-
cyanate number was determined by means of the titrati'on method,
and the deposition in percentage of thiocyana te was calculated,
The exnerimental results showed that the cis-form of the
fatty acids is more quickly thiocyanated than the trans form,
and that the free acids can be thiocyanated more slowly than
the corresponding esters. Quantitatively the thiocyanation
reaction of the cis and trans forms of elaidic acid and its
esters resembles the hydration reaction of these compounds.
There are 1 table and 5 references, 4 of which are Soviet.
Card 1/2

SOVA56 -56-5-35/52
o' ~,nd Elaidic Acids and Their Esters
,ISSOCIATTG~7. Kafedm -~rganicheskoy khimii Odesskogo tekh-
nologicheskogo in!~tituta pishchevoy i kholodillnoy promysh-
lenno.-lti
(Chair of Organic Chemistry at the Odessa Technological
Institute of Food and Refrigeration Industry)
SUBMITTED: November 25, 1957
Card 2/2

AUTHORS: Plisov, A. K., Zhila, L. A. BOV/79-29-1-68/74
. ................
TITLE: Structure and Properties of the Unsaturated Acids and Their
Derivatives (Konfiguratsiya i svoystva nepredellnykh kislot i
ikh proizvodnykh). X. Thiocyanation of Oleic and Elaidic Acids
and Their Esters (X. Rodanirovaniye oleinovoy i elaidinovoy
kislot i ikh efirov)
PERIODICAL; Zhurnal obshchey khimii, 1959, Vol 29, Nr 1, pp 323-328 (USSR)
ABSTRACT: Based upon the previous finding (Refs 1,2) that oleic and
elaidic acid as well as their methyl esters react with different
rapidity with thiocyanogen solutions and that the alcohol
radicals exercise a different influence upon the reactivity of
the cis and trans derivatives of unsaturated acids, the authors
decided to solve this problem by a thiocyanation reaction.
Apart from this, chemists are also interested in thiocyanation
and thiocyanogen compounds as they are used in vulcanization of
rubber, in medicine (Ref 3), in dye and inseticide production.
For this purpose the following esters were synthesized: methyl-,
ethyl-, butyl-, irobutyl-tert-amyl-, n.-hexyl-, benzyl-, phenyl-
and a-naphthyl esters of oleic and elaidic acid. The thio-
Card 1/2 cyanation of these compounds was carried out in reagents at

SOV/79-29-1-68/74
Structure and Properties of the Unsaturated Acids and Their Derivatives.
X-.' Thiocyanatio.n of Oleic and Elaidic Acids and Their E.-ters
various temperatures and in various concentrations. The results
given in the experimental part give evidence of the fact that
in the case of geometrical isomeric esters of the unsaturated
acids the cis form thiocyanates more rapidly than the trans
form. Apart from this, the influence exercised by the length of
the chains and the dimension of the alcohol radical upon the
reaction became particularly clear in the thiocyanation. For
the purpose of clarifying the cbemism of the thiocyanation re-
action, the final products formed by the thiocyanation of the
methyl esters of oleic and elaidic acid, i.e. dithiocyanogen
methyl oleate and dithiocyanogen methyl elaidate were separated
and characterized. There are 4 tables and 9 references, 5 of
which are Soviet.
ASSOCIATION: Odeaskiy inatitut pi clievoy i kholodillnoy promyshlennooti
(OdesLja Institute oflvod and Refrigeration Induotry)
SUBMITTED: December 4, 1957
Card 2/2

PLISOV. A.K.- ; BMVICTS, A.I.
Rhodanation of 91sic and elaidic acids and their enters.
Xaw-.h., dokl. vys. shkoly; khim. i khim. tekh. no.3:540-541
938., (Km ll.. lo)
l.Plredstavlena kafedroy organichaskey khimii Odeaskogo tekhno-
logicheakegs Instituta pishchavoy i kholodillnoy pron7shlenuesti.
(Oleic acid) (Iladic acid)

PLISOV, A.I~Q-WUTOVA, N.Y.
Configuration and Properties of unsaturated acids aul their
derivatives. PArt b: Reactivity of erucic and bressidie acids
and their eaters. Zhur.ob.khim. 28 no.2:498-502 F '58.
(MIRA 11:4)
1.0deaskly gosudaretvannyy universitet.
(Brucic acid) (Brassidle acid)

PLISOV, A.F.; PALADIYINKO, N.P.
. ..........
Configurations and properties of unsaturated acids and their
derivatives. Part 9: Properties of 0~.-methylcrotonic acids and
their eaters. Zhur.ob.khim. 28 no.2:503-507 7 '58. (MIRA 11:4)
I.Oelesekiy gosudaretvenW universitet.
(Crotonic acid) (Hydration)