SCIENTIFIC ABSTRACT PARSHINA, T. S. - PASHKOV, P. O.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001239310014-7
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: June 15, 2000
• Sequence Number: 14
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

ACC NR, AR6017565 SOURCE CODE: UR/0196/66/000/001/AO09/AO09
AU-LHOR: KtLlinina, T. A. Laz&reva, L. 1. Parshina, T. S.
TITLE: ~/ Electric field fit the mia of a conducting circular cylinder of finite length
with regard to the edge effect
SOURCE: Pef. zh. Elektroteklinika i energetilm, AI)s. LA72
REF SOURCE: Tr. 1)() teorii polya, v-1p. 1, 1964, 50-514
'DOPIC TAGS: electric field, electric theory, electric conductor
ABSTRACT: A rolution is given for the problun on finding the electric field (it tile
axis of a conducting circular cylinder with regard to the edge effect and special
cases axe considered. 2 illustrations, bibliography of 4 titles. From the summary.
[Translation of abstract]
SUB CODE: 09

CHERNOV, V.A.; LTTKINA, V.B.: SERGIYEVSKATA, S.I.; KROPACREVA. A.A.;
PARMUNA, V.A.; SVENTSITSKAYA, L.Ye.
On the antitumor activity of certain derivatives of the trimer and
tetramer of pbosphonitrile. Farm. J toks. 22 no.4:365-367 JI-Ag '59.
(MIRA 13:1)
1. Voesoyuznyy nauchno-isaledorvatellskiy khimlko-farmtsevtichookiy
institut imeni S. Ordzhonikidze.
(HETEROCYCLIC COMPOUNDS pharmacol.)
(AMINEOPLASTIC AGEMS pharmacol.)

AUTHORS: Kropacheva, ~,archina, V, A, S V", 1 7
TITLE: Derivatives (.f Ethylenirrine (i'r,)izvoJnyje eti1enirri~,,,,.
I Ethylenimides of Phosphoric Acid (I. Etilenimi!y fossforn)y
kisloty)
?ERI,'DICAL. Zhurnal obshchey khimii, 1959, Vol 2(), 2, ~,p c'6 't
ABSTRACT The derivatiNes of phosphoric acid are not only u!: e d i n
ag-riculture E-nd industry but also for medical purposes
Recently several papers h:-,ve been published on the activat.11
of some ethyl eT.imides of phosjJLoric acids inhibitin,- miall.-n-int
new groviths, Two of these, thc compound~z (A) an] "P) were
used in medicine In 1)')1) the authors bef7an their wore: ~~n.
the synthegir (.f the ethylenimine derivatives of' i-ho:lpholi--
acida They Intended to have t),(, compoundij thoy vivr-v to
obtain bioloti(-ally tented in c-rder to investij~,,ttv the
influence exercised by the subctituentstobe introduce-i --;in
maliUnant swellin,,2-s The first -,art of' the present papt-r
consisted in tY.e synthesis of
triamides of t~.e general formula 4 These compound.-, v,.*cr(,
synthesized according t~) scheme 1 In accordance with thi!,
Card 1/3 scheme the n-oYy-chloro iihosphines of the Lrylamines. '--

Derivatives of' Et 1, J e
i hosphoric Acial
no -,nalyiiis it c
t 0 e c n ::i i;l i ler.,v.Ltive f
The i n frar( 1 pe - t r rk? c r3 e i n A 1 ca t e d k 'V T h a
"I c,),m T ) u n dl r,,2 ? e I im i n o c y - I e s
Icn w s I t -i
A I t D~-It, t rier t ~ie rt r. t described di :' e t n i, a r y
am. ~~ :1 ~ s :-, f n o r : c a c I an-' f 4. ve 11 - oxy - c i-
N
0 f t ht- a ry a"-. r e -n t .0 s 1 z e T~~-re a re
., r o f i~ r t
I
ASS .-"C IAT I ON Vse s 0
~y 112 11 y 11 ~1,_ "in L I ~j L;: f- u t e I ;y ?himi f:.,r* vt
kiy inst.1tut imerta h,) nlkl;lz.(, I! - Un-, n L;c i-2r t c
:n9',It,_te Imen!
STUBMI'll'TED jjC.vpm,~)pj-
Card

'10761,
S/079/60/030, 04,
B0O1/BO1 1
AUTHORS: Petrov, K. A., Par3hina, V. A.
TITLEt Phic.sphatic Poly~stvr- and Palyamide Resins
PER10DICALs Zhurnal obshche.-i k1iiiiii, 1960, Vol. 30, No. 4, 1)1) 1 54, -1 ')4 6
TEXTt It was the aim of the investij;ation under review to c~:rry out
synthesis of organophosphorus condensation polymerslof the tyke of jo2yectert
and polyamides. Ethylene -lycol, di-ethylene gly-col-, hexamethylene diF.Einq
Pn,! the ester of the dibasic acid )is-(p-carbomethoxy phenyl)-methyl
ox.ide were u--ed for the condenoati)n. Polymers (1), (11), (111) are de-
polymers iz3 the circumsLL~rCe
,scribed The characteristic feature of these
th,,it there are atoms of pentavalen! phosphorus in their chain, wlich are
linked by phosphocarbon compounds. Thus, polyi-ners (I) and (1111 differ frcm
"Terylene" and "Nylon" by the f, ct thrit the r;-,!ic. !,,; CJ bi!> 1,P-carb~,xYph~on,,
r-ethyl pho-sphinoxide replace the radical of terephthalic ticid in the chaii.
the former and the radical of adipic acid in the chain of the other With
respect to heating and reactinE with various reaFents conti!ininC or-anoph-~-
U

Phosphatic Polyester- and Polyanide Resins S/'079/'6(,/"0710/ 04/ ~,7/Qbo
B001,'BO1 1
--rus
compounds, phosphinoxides ire the stableat, in contrast to the
I-es and phosphonates. The sy-atheois desciibed in publicationg
,~hirh yields complicated and bai Products, of bis-(p-carbomethoxy pheny,')
L-c-!'.yluhosphinoxide, was modifi?d and improved to a large extent, Thus, bis
(P-tolyl)methyl phosphinoxide w-is obtained in n yield of 62~ by the reacti.:'n
Cf acie. qichloride of methyl phDs:)hinic acid with p-tolyl mac-,nesium brc'mije.
Oxidati-n of ~,Iiorphinoyide was cni-ried out with aik~illn~
pernanE;anate (.yield ~C) Othf-11' ITS(-~:!]'ChLrs. Acid diehlorlle
resulted on heating bi a- (p- c,-.1-b )x.; phonyl) Lie thylphocphinoxide with tl.ion~'i
chl-cride. The polyester of ethyLene 67lycol and diethylene t7lycol of 1~,Is
(p-carboxyphenyl) methylphosphi.-ioxide (I ani II) were obtained on a
heat;nC Df methyl ester of bis-,p-carbomethoxy phenyl)methyl
with ethylene glycol and diethyLene glycol in the pres(2nce of zinc b-ra*~.
as catalyst and pentaerythrite. Transparent polyesters can be obtaine,; o:ij
in the cbnenc(, of OxyCen. By heating- in vacuum P salt prepared from heya
iicf.~iylpne di~,.mano %nd bir3-(p-car.)oxy 1..]iLiiyl)inotliylljliocil)liinoxidc,
was obtained, There are b referon-.es, 4 or whicli itre ';r'viOf-.
SUBMITTED: April 3, 1959
Card V2

5!rLs 0 210 0 430 1 6-j- S/079 6o/030/009/008/01~
BOW X064
AUTTIORS: Petrov, K. A,, Parshina, Y. A., Daruze, G. L.
TITLE: Phosphorus-cont,iining Polyesters and Polyamide Resins
PERIODICAL: Zhurnal obshchoi~ khimii, 1960, Vol. 30, No. 9,
pp. 3000-3004
TEXT: As was already previously shown by the authors, the polyamide- and
polyester resins cynthesized from diamines or glycols and phosphine
oxides (containing t%o carboxyl groups), are capable of developing fibers
(Ref. 1). The present Investigation deals with the synthesis of the hither-
to unknown organ o-phosphorth pDlymeralthat differ essentially from the
polymers obtained from phosphine-7x-ides. Tho initial substances of con-
densation were ethylene gl col diethylene glycol, hexamethylene diamine
and bis (p - carboxyphenyl~ pht"ophinic acid or its methyl ester. Three
polymers (I), (II), (III) are described. It is characteristic of these
polymers that their chain contE.ins the radicals of bis(p-carboxyphenyl)
phosphinic icid with the unesterified phosphorus group in the case of the
polymers (1) and (II), and in the ouse of tb-? polymer (III) in the form
of an ammonium salt. Thus, the first two polymers are weak acids, and the
Card 1/2

ERDPACHEVA, A.A.;.IARSHINA, V.A.; SMIYEVSKATA, S.I.
Derivatives of ethylenimins. Part 2: Ethylenimides of phosphoric
and thlophosphoric ecids. Zhur. ob. khim. 30 no.11:3584-3588 H160.
(MM 13:11)
1. Veesoyusnyy neuchno-ismleduvatellskiy kbiniko-farmatsovticbeskiy
institut itoeni B.Ordzhonikidze.
(EttWlenimlne) (Phosphoric acid) (Phosphorothioic acid)
10

KROPACIIEVA, A.A.; 14UIM-UIAR I, Yu.; KASP14IKOVA, N.M.; PAIISHINA, V.A.
React--*ons of esters of c~?rtain amino acids an piperidine with
the phosphonitrile, chloiide triumr. Zhur. ob. kbim. 31 no.3:103~-
1037 Mr 161. (MIRA 14:3)
1. Vsesoyuzny-y nauchno-issledovatellskiy khImiko-farmatsevticho-
sky institut imeni S, Ordzhonikidze.
(phosphonitrile chlor.de) (Amino acids) Riperidine)

25370
S/079/61/031/008/008/009
D215/D304
AUTHORS; Petrov, K.A. and Parshina, V.A.
TITLE: Reactions of Phosphines I, Reactions primary a I i pliat i(
phosphines with a dehydes and ketones
PERIODICAL. Zhurnal obshchey I.himii, v. 31, no. 8, 1961, 2729-2731
TEXT: In this experimental wori. the authors studied the reaction of
propylphosphine with formaldehycke, acetaldehyde, benzaldehyde, and
acetophenone; they proved that primary phosphines easily react with
different aldehydes and ketones. With formaldehyde the reaction pro-
ceeds according to the scheme.
C3H7PH2+3CH 20 + 11C 1 C3117P(CH2C If )3C1 With other carbonylic compounds
the reaction sometimes stops on the first or second alkylation stage,
it depends on the reagents as well as the solvent used; e.g. propyl
phosphine with benzaldehyde in aqueous alcohol solution with HC1 forms
propyltri-(pheny1methylol) phosphonium chloride, but in absolute ether
Card 1/2

25370
S/079,/61/031/008/008/009
Reactioflso~ Phosphines 1,... 0215/')304
with HCI it forms prnnvI(dimethYIol)phosphint, under the same conditions
as the last, only a secondary ph.)sphine is obtained with acetophenone-
propyl and phenylethylol phosphine; [Abstractor's note The authors refer
to aliphatic phosphines in the p'.ural, actuall) investigating only onc
of t hem,7. There are 4 referenced; I Soviet -bloc and 3 non-So,ie- bl"~,
The references to the English Iavguage publications read as follows
A. Hoffman., J.Am.Chem.Soc. 43, lC84, 192t.. A. Hoffman, J.AM.Chem.Soc.
52, 2_995, 1930.
SUBMITTED: September 5, 1960
Card 2/2

'WA 4/Pr
L':2 5 R/ZPA 5 M
RPL'
-:NR-~----AP400983l 0116 00/001/0020/0023
Jill
G Luzanbva 14 B.
Pbosphoizg_aa- soled -on'~Olyamidoph6sphinltes
TITLE, containing.
poj~~RMs ba
and Phosphites
rI
-77 0 S eticheskiyenassyi~j no6 -1 19'64,: 20"_
Ks _23
e r sam dation, d1kyl-
~s containing; I- po lym V,
PIO, Ti4g: . pho sphoru t an I
u 'diamide transaAdation,: arylthosphonous
~hotphoAo - ~'acid acid,
u
phorus containing polymex, bran clli c J
hlky1ph6�phorovts acid, linear PlId"
p s.contaiaing pol er, Pol!Iyamidophosphinite. polrw3r, polj-
VIOSPhoru YM
amid6phosphite polymer, ion excha`,~ae resia. f i:~'e resiatant irulpr`!~,
~ABSM .)f methyl- ands phanyl-phosphonous
CT-The-tetraethy1diamides~,
-i o rkicted with ethylene-, hexamethy"ene-,
and butylphosphorous a -war
-nz to them equation in the enclosure.
--..and 2-2h uYlene-diamineJoa~cordi'_
_.Trausam1dat1oh,qf :Uie mides of~ (a' lbbosphonous and ul'_,,y1-,
'Alkyl ry
sphorous acids with diames foilis high Molocular (23,600 - 53,000)
-'-'---,linear. compounds Transamidatior'~of theAndicated diamides with
lnea,~wlth & addition of htiraethyltrlamldbphcisphoTousiao'id,
am !Mama

7c:

01
i, iig--A-P4-QO983.L.

N(C~f is
+NHIRFN14i

L 6970-6� EWT(m)/EPF(c)/EWP(J)/EWIP(I;)/EtIP(b) IJP(c) JD/RM
:ACC NR; AP5028204 URCE CODE: IIR/007,a/65/035/009/1602/1606
AUTHOR: Petrov, K. A.; La=hina_,'_V. Manuj1o-t,_A.-L,
;ORG: none
~TITIX: Preparation of tetraalkyl(ar-r:[)alkylenediphosphine oxidep from methylol-
,phosphines
,SOURCE: Zhurnal obshchey khimil, v. 35, no. 9, 1965, 1602-1606
iTOPIC TAGS: organic phosphorusLcomp:und, organ.-Ic synthetic process
,ABSTRACT: A new method of preparation of tetra;ilkyl(atyl)alkylenediphosphones and
~diphospbine oxides is proposed in wbich dialkyl,(aryl)mf.-thylolphosphines (I) are al-
Ikylated by dibaloaUanes, the tetraa.Lkyl(ar-yl)dimethylolalkylenediphosphonium salts
~(11) are'dealkylated, and the alkylenediphosphines fonned (III) are oxidized:
Card 1/2-- UDC: 547.241 + 547.438.1

L 697C4~ . _ . ..- - ____ - ; __ - I __ - -__ . I
~ACC WR: AP5028204
2113P(CH2Oj1)+11B1(C11,7).t1ft1 --W IRINCII'Lph2Mal
0
njP(CH2j.PflS __* 19SP(CIIJ)'Pal
The alkylation was studied on reaction:; of dihepty.l-, dibutyl, and diphenylmethylol-
.phosphines with 1,1- and 1,2-dihaloalk-anes. The diphosphon-Jum salts obtained were
idecomposed with concentrated alkali at 50-70C to given good yields of alkylenedi-
!phosphines. The latter (tetraheptylmethylene-, tetraheptylethylene-, tetrabutyl-
ethylene-, tetraphenylethylenediphosphine oxide) were oxidized with air, hydrogen
speroxide, and potassium permanganate lc.acetone. The experimental procedures are
idescribed. "The authors thank G. F. t-adenkt'ligo performed the spectroscopic part
iof the work."'- Orig. art. has., -1 figu;-, -4tables, and I formula.
i
jSUB CODE: OC/ SUBM DATE: 13Aug64/ ORIG REr: 002/ OTH REF: 017
Cprd-?/2

L.2770"6 EWPOOM(p) RJA
ACC NRs AF6018512 wtmcz CODE.- UlVO09/65/035/011/2062/2065
AUTHOR:- FetrovL K. As; ?Arahima, V. A# I Manullov, A. F.
ORG: none
TITLE& Production of dialkylpethylol i(Ephines
SOURCE:.Zhurnsl obsbehey khimli., V. 351-no. Ili, 196,9ij, 2D62-2065
TOPIC TAGS% alkylphosphonium salto al)ZrIphosp nev bromidej, alkylationo alkylphoo-
phine oxide# hydrogen peroxide
ABSTRACTS 'D1bVty1-4~d dibeptyleeibylolphDaphines irsis yrodueed In bigb yields
1~'by the reaction or triseftylo1pbosphlike with butyl and Ikeptyl bromides,, followed
,'by eourersion of the alkyltrImeftylolplosphonium lbrmldes rorxwd to alkyl-
~61setbyla1pbospblues througb the action or triethylawlse. BeconUry al)Wlstlon of
Ahe alky1filseftyle1pbospblues yielded bromMesp In
Ibitter ylelds wben the reactions were voMuetea at 6D-70 . AMWI*tlom M W
learried ant both without and with a solvent' (alcobols or alkyl bromides). DIalkyl-
dimetbylolybospboulum bromides . just I Ake moncelkyltrimthylo1pboapboblum brould" 0
Is" deernic edby trietbylaulne to dl91kylmetbyo1Vb*m;blww. TM metbylol-
pboapblues odd sultur to form a hr1o1pbR!j&1sq Igtides. 9'UA*r the actlas
at bydrqps peroxidt, the dialkylsethyla1pbospblues m axldl~bd to 6161171-
Vieftlallimpb1twx oxides,, the letter bebW converted to Vw
lft OxIdes &atlas UT ft~*Rrl emerldso
orig. ari. has 1 3tables. &H-97
SUB CDIZ: 07 / SUBM DATEt 13Aug64 DRIG IREFs 004 OTH IMF- 001
Card -111 -(1 ry

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. , ' -7." 1 -1 " . I. - 1, ~.. ~ '',
, f~. ". ~. . f

KROPACHEVA, A.A.; KASHNIKOVA, N.M.,--PARSHINA , I.A.
Reactions of phosphonitrile chloride trimers. ?axt 2: Interactior
of a phosphonitrile chloride trimer with glycj-ne ethyl ester. Zhur.
ob.khim. 34 no.2:530-5311 F '64. (MIRA 1'7:3)
1. Vs~sopjznyy nauchno-i s E led ovate l'sk Ly khim.ko-farm&tsevtiCheskiy
institut imeni S.Ordzhonikidze.

PETF,DV* K.A.; PARSHINA, V.A.; TSYPIXA, G.M.
Phosphorus-containing pnlymeri3 based on met-iylphosphims and
methylolphosphine oxide:i. Plaat. massy no.Ll:11-11'''63.
(MIRA 16:12,'

PEMOV, K. A.; PARSHYNA-,-.V. A.; ORIDV, B. A.; TSYPIIIA, G. M.
Properties oi' phomphinets. Part 5: Reactions of phoephinee
with chloroamines, aulfonyl chlorides, and aminee. Zhur. ob.
khim. 32 no.12:4017-4022 D 162. (MIRk 16:1)
(Phosphine) (Sulfanyl chlorides) (Amines)

MUKHINA, A.YE., KASHNIKOVA, N.M., -AR3HINA, V-A-
The replacement of chlorine atoms Ln phosphonitrilchlorine trimer
by amino compound radicals and the biological activity of soma of its
amino subatitutes.
Kldmiya i PrArreneniye Fospomorganichaskikh -Soyedintlniy (Charydetry ar-ri
application of organODhosphorus corinounds) A. Th. AR117PV, Ed.
i'ubl. by Kazan Affil. Acac. 'Ici. USSR, Moscow 1962, 632 pi).
Collection of comolete oaT-eru Presented a, the 1959 Kazan Uonfc-r--nce 3n
Chnmistry of rranoDhosp~Krun Cormounas.

SAZONOV, N.V., PARS14INA, V.A.
Ethylenimine derivatives of substituted phofiphoric and thirphosphoric
acids and their biological propertl-es.
Fl-imiya i Fosfr,r.)rj,&niche-ikikIh Soyedir.-My %r-,
aDulieLtIor, of orp.:iw)r)ho-i0Y-,rus co,1t)ounA!q', k. YY - A -1 ~-(i.
lw)l-, by ~Ia.-Lar Af CII Axor , cl. Mo3~-L)w 1962, 1 1,1 :)t
CnIlm.ction of Da,.,!ro ~,rnnented qt the 11?~") Ka~.-wi ,
cl-~-rtlntry of Gonnourrcls~

PETRDV, K.A., PARSHINA,- V.A., DARUM, G.L.
Ptiosphorus containing polyester &ad polyam3de resins.
Khiraiya i Primneniye Fosf:)n)rganicheskikh Soyedimniy (Chardstry and
application of organophosphorus COMOUnft) A. YE. AI?317DV, Fd~
flubl. by Kazan Affil. Acad, ';ci. USSR, Moscow 1962, 632 PD.
Collection of comlete Dapfirti Pmsented at the 1959 Kazan Gortforence on
Chemistry of :rvanoDhospharued; Gomnoukds.

V. A.
-5"
PHASE BOOK ENPLOITA rjON SOV/60114
Konferentsiya po khimii i pruneneniyu fnsfororganicheBkikh soyedinenly. 2d,
Kazan'. 1959
Khimiya i primeneniye fasfor-)rganich(skikh so~edineniy, trudy (Chemistry
and 1,*,;e of Organophosphor is Comp~)unds, Conference Transactions) Mos, 0..
Izd-vo AN SSSR, 1962. 6:0 p. Errata Llip inserted. 2800 copies printed.
Sponsoring Agency: Akadem))a nauk SSSR. Kazanskiy filial,
Resp. Ed. : A. Ye. Arbuzov Acadernician, Ed. of Publishing House: L- S.
Povarov. Tech. Ed. : S. G, Tikhoinirova.
PURPOSE: This collection ct conference trannactions is intended for chemists,
process engineers, physiologists, pharmaciolifl, physicians, veterinarians,
and agricultural scientigti.
COVERAGE: The transacticris include the full texts of most of the scientific
Poalpr-rl~ presented at the Sfcond Ccinference on the Chemistry and Use of
a4,~ 111 4_

Chernisti-v and the Use if Organophosphorus Wont.) SOV, 6,034
Organophosphorus C )mpounds he ld al Kazan' from 2 Nov through I Dec
The material is divi( ed into three se.,tions: Chemistry, containing 67 arti-
cles, Physiological Ixtivity of Organaphosphorus Compounds, containing 26
articles, and Plant I rotection, containing 12 articles. The reports reflect
the strong interest cl Sovie-. scientists In the chemistry nnd application of
organophosphorus ct mpounJs. References accompany individual reports.
Short summaries of some cf the listed reports have been made and are giver.
below.
TA13LE OF CONTENT.i [Abridged):
Introduction (Academi( an A. Ye. Arbi. zov) 3
TRANSACTIONS OFTHE CHENIISTRY SECTION
Gefter, Ye. L- [NII pli.stmass (Scientific Research Institute of Plastics,
Moscow 1. Some Prospects f:)r the Industrial Use of Organophosphorus
Compounds 46
Card 2~4

PETROV, K.A.; PARSHINA, V.A.; -LUZANM , H.B.
I
New method of synthe3:18 of tertiary aliphatic, aliphatic-
aromatic phosphines, imd methylalphosphi-nes. Zhur.ob.khim.
32 no.2:553-557 F 162. (MIRA 15:2)
(Phosphins)

FETROV, K.A.; PARSHINA, V.A.; GADAUK, V.A.
Reactions of phosphines. Part 2: Reactions of primary aromatic
phosphines with aldehpies and ketones. Zhur.ob.khim. 31 m .10:
34-U-3414 0 161. (MIPA li,10)
(Phosphine) (Aliehydes) (Ketones)

FETROVI K.A.; PAR~HINA
-, ___ , V. A -
Reactions of phosphines. Part 3: Reactions of second-az-.f phics;~~-`- s
with aldehydeB and keto~ies. Zhur.ob.khim. 31 no.10:3a7-34210
0 61. (MIRA 14:10)
(Phosphins) (A-Idehydes) (Ketonea)

BUMP K.*.; PARSHINA, V.A.
P4ACtionB of phosphincia.. fhrt 4: Properties of mothylolphoaphonium
chlorides and methyloilkhoaFhines. Zh-ar.ob.khiin. 31 no.10:3421-
3424 0 161. (MIRA 14:10)
(Fhosphonium comfounds) (Phosphine)

PETROV, K.A.; ~AR~MINA, V.A.
Reactions of phosphines. Fart 1: Reactions of a2iphatic
phosphines with aldehyde.3 and ketones. Zhur,ob,khim, 31
no,8t2729-2731 Ag 161. (141RA 34.8)
(Phosphine)
(Aldeh:rdea) (Ketonev)

J -~ 9'.-1 C
S/079/62/032/002/005/0 1,1
1)2?-7,'D.301
AU'rHoRs Petrov, K.A. , Parshina, ~ A,, and Luzanova~ MAi
TI ME A new method of ki'Y,ithesiting tertary
phatir-arom'stic And Inethylol -P~osphlnes
PER 100 1 C AL Zhurnal obstichey kh Imi i , v, Do. 2, 1 96-1 5"1 "51)
TEXT ~ Synthesis of methylolphotiphinef-i and phosphonium chlordes W~tj'
alkyl- and arylalkyl radicals j-3inted directly to phosphorus, and alao
tertizry aliphatic and aliphatic-arom,atic phosphines, is decribed. The
starting material for the synthesis was trime1hylol-phosphne which was
obtained from tr,,ethylamine and tetramethylol phosphonium chloride, By
the action of alky, halides ano b--nzy) chloride on tr,.methylol phosphino.
alky'- and benzyl-trimethylol ohosphonium halides were produced which no
removal of one methylol group, converted into the correspondng dimefhvlo'
phosphines, By repeating the re-actions the authors were able to obta7r,
monometliylol-phosphines and trialkyl (tribeniyl) phosphines. TF.-Methy''),
phosph:ne was prepared by otirring tetramethylol phosphonium !chloride
Card 1/.3

was=
3 !9-'
A new method of ... 1) 227, / L) 3 0.3
and dry ethylam, ne at room temperature i n ni t r aKen foll lowed b~ heat . niz,
0
to 60 C for 2 hourtA. Piopyl trimethylol phosp!ioniusk b7olnid- was ple'llarod
by reacting trimethylal pho&phtne with propy' bromide at 60 C ;n t).trovt~r-.
Propy! dimethylol phosphine and dipropyl dimethylol phosphor.um bromirif.,
also d~propyl methyXol phosphine, tripropyl methylol phobphonimn brom,cl-
and triprepyl phosphine were prepared by analogous rea~-tiorus- In the
matic series berzyl trimethylo' phosphonium chloridC, berz 'v) dimvth'N!,~'
phor.ph!ne, djber,;?yI dimethylol ph(,sphoiii~jm chlvride, dibene*v i ill C. t 11.~ I -) I
phosph,-ne, tribenzyl milbylol pho&phonium khlorid,~ ard it A(m?'N'l phosphr",
wer,. SIM-Aarly prepared from trimethylol phosph.ne arid here,.Yl ~hlortd-
The mtthod &yr*her,' ~:ng lv!liary ~,hosphtrep a baLzed on a'k.,, I at , )- --~ II
m r ! h y 11 c ' ph o s ph - n tLs ar d daa 1 kv I a t , or o f m ? I h v ~ o ! p ho s p ho - u m 11 ~1 ! . J JI)
t C! S gener a, c harac t er mav . t lieref or bP ASed for pr-du :k, Q J q
ar gan9phasphor,j!, c umpoondf.; wi I h o - f f e-r ent f vin- t : onal groups There al-F.
19 reference& 6 So% et-.b!ac and 13 non-.-,ov e* .1,11o.-. . The 4 mos, f-- er.-
r e fer e nL e:3 t a t lie Eng I - sh. 1,m guag,, put) I i c a Icns r fi ad j s f o I I ows IV, A
Reevee F. FI vnri and J D. Gut hr i e , J Am.Cherrj.b.)c 39, 3 ~ 19551 A
Buckler J Am.Chem--;o!: 82, 421 5, ( 1960 1 ~ M, Reut e r kind L. Or t hn-
C,r d .2,11

S/07 9/6 '2/03 2/002/00 5,~O 11
A new method of ... D22?/D3(13
M A., 54 ~ 14124 1 ( 1960) ; Six. A. litick I er and N. E. UOY, C It -A - , 54 , 15.1 H,k-
( I c)60),
SURM IT rED January 25, 1 961
Card 3/3

TSYKINA, N.F., inzh.; PARSHINA, V.I., inzh,
Casting rolling-mill rolls of boron-alloyed cast iron.
MashinoBtroenie no,3.,52-54 Ivy-Je '63- (MIRA 16:7)
1. Lutuginskly zavod prokatnykh valkov.
(Iron founding)

rx
Va.
BELIGOVSKIly VA.; PARSHINA) V.I.
Increasing -.he h,--rdr~esL :,.' Is for --ne lzd7;5tz7. ~
no.4'.4 Ap 10. 1 (ALT ~A , t : , I
(Paper-mdu;ig kuist lroji) (Gwe hardeniag.)
-71

GWTOV. V. V. , inzh., LTSENKO, , N.A., inzh:; YMSH11M. V. H. , Ingh.;
SOKDWVA. N.A.. Inch.: ISADSKAYA T.A., In-th,
Economic effectiveness of centralized electric power suppI7 to
logging camps. Ankh.trud.rab. 12 no.1,2:29-35 -D 158.
(MIRA 11:12)
(Li2mberIrq,--%rh1nery) (Eloctric prwer distribution)

V. V. '.v s en k o, "'. A. , 'ar s
.otov 1 na , V.
:salska
,y
T E 'he -con~,-nical '-!'fectixenesE Df a 'en*ral~ -e~
u 1,v r -n ~ e :- i n g 'i t e s `kDnomcheskaya f't- e F. 9
t s e n T, r al i z,) v an n 1 t- k t r ~),qr Fi 1, z he n a e R K
AL - .4ek-anizatsi-.a tr,.~i~yeakikh i tyaz-.., K h r a',- - t
7 Z,
pp
A r~e ar- cle lea s ,:. Jetal I wi th t;~e calc,-~:a *.l,.,,n '!~c
p c -. a t r. Ei e x r, 8 E~ s a t ~n 1 e r i n g 3 1 t a s i n g e re c r
p D w a r i n s t e a I - 4 11 d r i v e i. e n gi r e s . "~~e researc,~ le&4.s
t -3 c ~ n c -; s i a r -in j e r d re f i n i t e ? -D r, J i t i o n s h e I e r - -
c a - i !- r, o f e I m b e r i n g i r. d u s t ry p r 3 v e s t e c n -
m r e -2 f f i c 1- e n t a s Tn p a r e d Y, i t h t h -3 U t i 11 7 R 1 T I C
-pre are tab.e3, an.-4 gra-h
ed mechanisms.
ard 1/1

FIFY Or c I:If, t, r L.

PARSHINA, V.P.
Mental disorders in bronchial asthna. Vop. pailch t nevr. no-3:
66-74 158. (NIRk 12:3)
1. Iz 11 Leni47,radskoy psikhonevrologicneskoy ')ollnitsy.
(ASTIHM) (PSYCHOS-33)

GORELIK, B.h.; MAYZEL'S, H.G.; PARSHINA Ye.,, .., . ... _,
.
High-termernture "Icanization of rubberized cloth by means of
infrared rays. Kauch.i rez.16 no.g:'L-9 S '57. (MIRA 10:12)
Nauchno-isaledovatel'skiy institut rezinovOY Dromyehlennosti.
(Infrared rnvs--Industrinl aDnlicntions) (Vulcanization)

ZUTEV, Yu.S.~,PARSHIIIA, Te.A.: GRIDMIOV, I.T..
.
Methods for accelerated aging of rubberized cloth. Eauch. i rez. 17
no.9:27-32 S '58. (MIRA 11:10)
l.Nauchno-iseledovatellakiy institut rezInovoy prou7shlennosti.
(Rubberized fabrice,)

'c' I i I VSFly' R. ( K"j V:ik.Y, 1'. K: ESKEN , I.[ K I emen, NJ 'V?AAYYLft, V,
!,'I, eunmj~~r, V. I, -~RAbETSK I"', Z. L' RE'., ;~'. 7.
ftranslatorl; '.F'A-aSJ:flNA, Ye.-A -.ftranslator]; PETt,."W', V.Yzi.,
gene rai -1 eyteriant, red. ; Airl EWV, A. 11. , ~-ed. ; VITHANOVA, M. D. ,
tekhn, red.
LNiglit Iif~rhting)NUCIPIOI bli. PL,d red. P-Arenko V.IA. Mos~cva,
Voen-,zdmt, 14u.). 1'7( p, Abilcj-f~d tran lation from the Czech.
(Ml.~(A 16:2)
'Nipt-A fightir,g kMilltery science
k

60V /13 ~- - - P - ~! I -

UTHORS: : (-j .T
A,; ridi
Yii. 1j;

TITL'T: ?.'.etiwA of A--(-ele r~.'-e Ie in-v i e i
,MetodL!,a us'-c,rer:!'OLO starerd'.'~' prorle-zinen-.'-
PER1OJlCAL pi) .' 717 M3.3
1. 1, ~
1 ~:'
, h,
1, 1 lie ', i na
Lau
: z
..
,
,
,
ABSTRACT 'Und_~r atmoLipheric conditions, a,'eli~- of m')- er T-
.
-.e
is due "o ozone and I,. cin, tl,e rc. bore
.1-at a, of ru;~,er :Cubric3 fL- r-. 1.1
C-111SE11 ~n7 t'-:e _P_LC_or,-. ?e rtj, sn 1', t e t s
on t",e ef"ec!, cf ozone on ruh)er coated filbres
)unlislhed z;o far-, Lind tj-,e aut-.,iors i-vc_~tJra'
I
of ozone --,r)..] li-liu -.rd Character of
ace' fv of tl,,e3e T!iey also 'o,..,--1
'L ~
-
qi_,'an'_It-_,tIve ev-.l!:-t' ior. o' L'-~H c m

';-a3 ev~luutcd by
T he e
c I') i I e sl-, e i te r i -11 s ri i f ~e re IrI
p 3 c ru b C. r 3 e r- Oy a ~A r.'d
'
dinc to I-, e-o:pi,csition o-Ir' t'-e -~Iseons 1 L:.'er (1a,
",tj nf o.~one _tz i ',~_e !31
IaA
,
lint~r_._ticn of o7one un,i 1i, ht, on g,tt~,rlaj 11 ~,ti
-ard 1/4 to stretcl-iin~ _L~I c rt I i,,:, d ( 100 Im n i

-ib,
blethod of A,- ce I e ra t I
-11 j U r -
weft (A i-s i., Tal-~le 1. TI-(, e T-e
L 1~
of Lhe rubber-c~., iuel 'a dul'ir-L
influence cf' v-Lrious tensionin-r- vn,~ur
ditions is Liven in a r_raph (FiC.1s.). T-~e6e resulL-s
cate '6!~at an increase in the tivo-di:qeTlSional tensioni,k:
causes a decrea3e in the aL,:e3nL st~..billt- c~f n4b -ei -
coated -.-iaterials- F JE. 2: ch ~1. n~ e s Ir tl.~,.,~ s -e r:- e 01
of i9 at e rial la ;u. r i r-4_ a,, --~ i ri[ u nde r a t:: c, s, C I t 1 6
when 1- and 2-dinensional tersionirQ. is aijplie,i. It
be observed that under t:~e act-ion of
sionin(, t.",e materii-il a-c.,s much faster thar, C.",'P-
dimensional tensioninL is applied. "lie efre- c.' tp,~~,-I,
in,E on the rute of a-ein of -later'.als la
acceler,-~ted lj-!,.t.-ozone g~~,eirC, -vher. concentr:-t' -' r,
of ozone equals 1 x 10-3/' for riaterial la ,;4r-I 1-'x io-,
lor material 2a, is river. in FiL.3. 1he
depends to a consiJerable exierA I e 1 ". t
-~ I - ~ I .-
sunliFht raJiaticn. The unit; of (,~qulv:..len~ slIMIT'(7~', I J. 9
(ELS) adoptel. The coefficien-IL; -n P
mar nitude of siinli- ht r'- ii~Ltjon we ne defi,,o(I Iy
re nt s (Fi, s. 4 and Tlae ,,onci..:~-.ration of
Card 2/4 pheric ozone is con3i--eribly lo,,-.,er in t~-.e

sov/l-~O _C;
wethod of Accelerated A_e'Lri;- of ~tubber-Cc~:,tt~--; r
of the mbber than in the surcounUin!- -.L'L:;~cs,i1-.v, re. S
is to be ta'.,en intc, ac-ount .'-.en evaluatin- ;?f_-!
iency o' t,,,e Tubter-coaled -,-,ateri 'Ll s (Fi~ L
The a., ein- stability of rub~)er-coated :-,a~.evials a
in~, UTIder atm~o sgl-.e rl'. (; ond i'. ions , w-~ s m i,,r i i t L,
estim,-_~te:! at EO C, anA, the intens1ty o~ tlie 1i' "t L3
appro-cim'~Ately tviice that of sunli,,--ht. Die tezt:; vi',T-
carrie I out at ro on ter,p: ralure CA
renWed c oncent ration of ozone wis foun,,! tc)
10 for :-~Iat- la :.,nd I X 10-D/'-" foP `-.4teV.11
- "4
v
"omparative results of ar,~~eler ted anl ratural
cf various rubber-coated Materials are t"~'W te.1
ird 7/4 2). This -ethod can also be used in industry. T*~ r,-~

.'CV/1 7)
i.:ethod of A.--,,e er-te~i
are 2 7ahles, 10 :FiLi r(,,-,
and F, 6,-)vLei.
,%3 ;0C, I A -I I C I ~: I I' al-cl, nc -13 3": 1
( ~;' -' (Scientific Re.3ea.rch Institut,-. of' the Rubber,
Industry)
Card 4/4

30V/13B-511-10-7 '10
Ar 0 a 5 Mayzei's, -7!a*.-ev3'-iy, V. -;; P-.rs',ina, Ye.
TITLE: Butyl Rubber 1. The Pri"C'Lj1e3 C~
lishia~, an Zconoi~ic~il Tec'.-,nolocy for t'ie Productl~-n of
Rubber Products Based on But ',-I i~)bber (Prin'Lslip-1:
yeniya ratsional'no,, te'linoloLil proizvodstv.'~
t,e'rhnIche:3'-.I'--,h izdelly na osnove butilkauelhu'-a)
1
PERIODICAL- Kauchu',-. i Rezina, iAr 10, Pi) 11 - 15 (V35'd)
ABSTRACT: Durini,! invest 11_at ions of t'-.c- above principles, butyl ru-.)ber
it B" wibh a molecular %lei-'!-.t of ~`,000 vl,is testel. PlAstL-
cisation of butyl ml)')er -.-raa foun,1 to be ineffective )e-
cause of the hiCh deC-L-ee of saturation of the mibber
may cause de3tructive oxi,:~-ition- Several proces ;es,
such as mixinL, refining,, cilenderin- and s,)rayLrC ci:-
be c-,rried out at Increased temperttures. Inve3tLL L.-ions
on tne pro,)erties of luty:- rubber ~Axtures shovred tl-,ut t~-ie
load rejuired for 2ausi deformation decre tses 31~-,'r,)17 -1~
L 'T LA. Or, comparin,~ "ie tempera-
increasi--C
L-7re dependence anal chux-_-,~z, of tt-,e elastic prop~~rlies of
analo,ous mixtures of but-il rubber, an-' a nu,:-,ber " ')t~~er
induArial poly,iers, it found thit t-ie d,,,Ior '.ion
butyl rubber, a Ci-.-n temperature intervLl, Is
Card 1/5 c:iar-tcteri3P I -)Y t'-,o loa I ~tnd the reducirie, prop~2rL .1,2s

SOV/1,5 9-5 1. _10--1/10
Butyl Rubber (Brtilk!Aurhu`)- 1. T),,e Pri ~ii)les of a~
TZoononAcal Technoloo, for t'.,e Pre tucLloa of _Zub')~r Froduc, 3 13aje!
tests ,;er~:, ir, i
lar
m i 7 ,,1. re s (7 .
on 'Jutyl it'-.f?"Ilves !r
and smallcr of fillers. This procuis -ol)l,l
carrie,l ouL 7hen the of :'ie
75 )1~' I Lives i on t!-,e ~ri, r C)-13W7.,)
o~ i ~riot_ia i'~'t)ras -i(
jjjr1nL L I ru)')e r !~
cont-AininL fillers. T)-'t. &,illmum teinp,3r;.~.ure C-.e
I
be- i nn I ri,~ of t ~ie ,q I n,, p ro c es s aa s f ou n I t o be ) f t
der of 1000 , , ' I -
r ;:i sub sc-,~.t i,e n t, I tic re ~i wi of it t,f- !,p! (".4-
o
ture to 120 -130()C. Sulphur and thlt~ram is led onto
the rollers. E.i-ctores 75 1z c-irbon -_)uld
3 - 10 n
be pred--Arad in , Inu'.ej. -lie mixtures could ))e
homoZpanistj 1 jcj I )url.11L~d ~)7 re'lriln~_ and ~;*, -,
theY coull e isily '-)e caleilipred. T h a a I i I -_ I on
ro'
in is r,?com--:er,1-?1 t~, iir:.,)rove calenderit-C. ,ae Optimum
temper,iti;ron of calenderiii, .,i,~ret temi)erkl-urc c,,~
to,) rolltor 7)0 - 1:~Oo., of. tlie T.11 Ile roll ?r _)O - 110
and of t.- 'ootte-.-, rnlle-, 10 100c),,. '211(- Ai:,L I,Dr.
Card 2/.g , 1G - 1~ ' c.' -a -nixtur,,, ~Is(,
fillers,

Butyi iub',er. 1. 2-~ e P rTI E- __ C f r Z C o n C
ncloL7 for the Iion of Pr~Dlt,.L;
ir.~.roveo (,on A'i,, icr.~~ cf7ile r-1, rinL And imp 4.r' t 0 e
c o, ! t i nL -.' sr-not-h c;ur'-z(-e. ',*',.e temper.-.Lturf- con.~i'lc n5
of the rolle(s shoui-I be chan.,,~ell to PC - 120ov"
on th.~ top roller-, 5U - ;100k.' on the middle i-oller ind
70 - JOOOC on the bottom roller. The terp rature of
calenderi ' tnflu,2nc~s tl.e bonJ sty-rLt~i of the n:b'~-r
u A
mi~:ture (Fg.3). Spr4yin~_ nO struinl% of mlxLure~, based
on butyl riabber is only pos!iible at hiLh temperatures.
The mixtures shor., a tenlency to 3ediment.,,ttion. 1.: i,~t U re zi
not containing, iry fillers '-iave 65 - aS~_ sediments acccr-
din~, to the ',ype of rubber :sel. Li-ht. fillers such as
po-adered silica gel, tjtanj,,,Tr, white, calcium sillc~ate
and chalk or carbon fillers decrease the amount of de-
posits and improve the surf-.Lce. The addition of plasti-
cisers improves con-' it ions of sprayinL. Adhesilves b,~Lsed
on butyl rubber uan easily :)e prepared because butyl
rub'..er sho~',.i ood solu~,Ility in aromatic hydrccarbcns,
and also in petroleum ether-A graph shovis the effe,--t rf
the treatment of textiles ind the strenrth of the bond
of calendered su-)st,,.-,ces But-1 rubber ~tdhesives
cannot be rixel -;ith ad'-esivPs bAseJ on other polymers
Card 3/5 because butyl rubber c-Annot be vulc-,nised in the presence

30V113
Butyl Rubber. 1. The Principles of Est--blishin', an Ecoronic,_l Tech-
nolo,r,y for the Production of Rubbev PrQit:t6 B.Lged or, __-,U'.y1 .7L-~ber
of unsatur.,.ted compoun,I.-- 2he ti!r,, required _'cr vulc.,i,
Isin mi-Aures b,sel on `)O)l rubber can be sho,tenel
from 45 to 50 minuteo 11c, I- ninutes when inCT' _Sl e
vulcani s,-itlon teT7p- rature from 143 to 17,00C (Foi
The stren-1.1i o-n Cle but.-,rl rubber vulcanisates :ind c,-~er
,polymers is af_'E,,,ted by tlir. tem,-ruture
(Fi .7). A s,,oT-t(-)- t Irie of' vulcanisat,icn cjn ilso b--
--ichieved by incr~--.-sin_ t'-e ungattrLL,ion of ~~.e brt,I
Iii-h nulity nbberlsej sut)stajceLq are by V-,I-
canis~Jion. The con'Ll-tout; vuleaniser "B~r.itor_rll
used In t, 'ese e,(,er-IL:n-As. Optuimi,r condlAon:i of
sation of rubbe.,isel subst.i.ces bused on butyl
ure tabulated (Table ~'). ODtimum conai'.Iona for rroi.llel
Card 4/5 articles from '~,,A%l rubber arz- listed. There re

6OVI 13R-5 q-10-1V 10
Butyl Rvb',,cr. 1. '"h,; Frin,,Ipies of ~,A-ALlishin,~~ an Economical Tech-
noloLy for the Prodrction of Ttub'jer k-oflucts Based on Butyl Rubber
7 PlZurEIS, I Tdbles und a rieferences: 3 Soviet, 2
'.TrV~llsh..
ASSOCIATION: Nauchno.-issledovatel'skly institut rezinovoy proM7-
shlt~n-oatl (Rese,~rch Institute of the Rubber Industry)
C a r1 9/ 5

AUTHORS: It',ay?:el-'s,
TITIZ-. But7l ltib~)er
Effe "'-i 'E
I I-, .~ t r ~, -~5
PZRIODICAL.- Kav~h,.J, !
ABSTRACT-t
Card 1/6
Ll. ~; Tt,-'
1,IP-,'11,~au..~.0:).
M, , 3 1 t I -, nS 0 f
ra ' 4- -, r. a i ' n,,-'T
E-7--ni. jr:r,, Nr
SOV/138-58-12-2/17
and-Zarshina, Ye. A.
Principles
t,b b ~ r L: i x t,,i re 3 (Pr 1
T'e t s e jp t u ry re z i n ov y k h
1. Pp 3
At prc-serit, Lhi-a,,; tyi,e,3 )-f 1,utyl rubber (A, B anl ar-~
use.1 in Industr,, "~-.-.h dIffer by their mole,.~ular
(A n,-t 1e3.9 --X),000, (B) not leis than -3~,000 an-I
01 n,','t 1,3ss th:an 30,OOG. r1he technolo-Ical, as a-i
phys!-~c-me,,hani,~ai r' -Istics
t e of vulcanisal - s. r--
relative ancl el,~)rcation, wear and tear res is
and adlhesive proj~ert-le-3) de~* )end on the molecular
The varic-ug ti-!ies of Uiree tydes of butyl rut-)cr ar.:~
de S C r1ij e d -Irnrest!.La~-',,ns shovied that the bond 3tren-t'-:
of rubberi lr,reases with decreasing; molecular weiLht ol
the butyl rubl,,--~r. ThI3 dat3. a6rees with tI,e -ont,~mp(ric;
theory or, thealhe-3i,-~n of hi--,h polymers accordinC to
the bond strerk~c~, of 1.,olymerio material depends or, trw
difflusion of t~,-.e !.~P-rmirial parts of the moleL~ular
(Ref.1). Vari,~w~ of vulcanisation af_,onts w-2r~
te, sted an! the o- ne,--hanic~ll charrkcteri,3t 1,~ 3

SOV1136-5b--12-2117
Butyl Rubber. Prin,'~ipleB -)f Fcr-j-~ Effective
Rubber Mixtures
butyl nibber vul-anisates, ccritaininC, an oitlm~.tl -viil-
canisation Eroup and vul,,.anised at different tampera-
tures, are shovin .'r Fir.l. The most suital~le Tix' -u re
was: 1'0~.thi,.~-vam and ca-ptax I-% A 'urt:-,,~r
Increase in the a:iio,,int of accEslerator Is not permissl')1e
because miera-tion occurs. The effect of various filler3
on the mechanical properties and thermal stability ef
vulcanisate3 was Investigated. Butyl ruln-)er is a ,rystal-
line polymer and. U-terefore, the Introduction ~-f a'tive
fillers does not in-.,rease the streriLth of the vulc:-:Lnis~ltles-
The addition of fillers increases some of the phys'le..--
mechanical charwteristics of the vulcanisates and their
stabilityto aLelnr and tc aggressive medira '. and also
ensures the requ ir~~.j quality. The addition of furna-.E)
and lamp black de~,reaSe3 their break resistanoe, b)it
to a 3111,ht depree their tear resistan~e-
Carbon blacks in(: re-aae re sistance to a geine. hardne s 3
and elasticity. powdered silica gel, 1caolin arJ
titanium dioxide -are most sa'~isfactory as fillers.
Table 1: dat~i on the charanr-,erlstic influen-e of a rium-
Card 2/6 ber oil 1Lht filler.3 on tie I)asic phyaico--m-onani,'~al

SOV/138-58-lZ--2/17
B=1 Rubber. Principles o,-" :IonnulatirL MA-fective Comri;c-E'L".cri
'Fbib er Mixtures
characteristics of bityl r-ibber C. Butyl rub-)Pr sho, is a
hiC,h de-ree u-1 -~-,--,-ir-Ation ind, therefora, S-bonds aze
of less Importan.:(! durinL the formation of the stru:ture
of the vulearlsate 'than In rther unsaturated rubbers. The
thermo-stability of the rubber is incre-naed when '~O - 60/~O'
of gas c'nannel is added Relevant tests
viere carrIed cut ~n the ter.,.P~~r--ture interval from tT50~ to
1500C. The tear -L,-ld break resistance are also in,-i,eased-
(FIE . --- ) .The -VALLIor. of .t.-hite fillers lncr-~)Lses the
stab.111ty.. to a n-u,-h lesser degree, All these filler.,3
decrease Lhe fr,,.3', v.,:3isttnce of vulc;anisutes- '12'ne cnef-
fi.,:Ient c'L -.rL..it ri-sisttnoe at -45r' lies bet'ii(--~n 0.29 tc
0 . 32' .FillerLj al.io influence the ves~stance of the vul-
canisates to aguiri,~. Table 2: data on the (.-haoteristi(-
aeein,r of vulcani,:ate6 ~ontaininC 30% channol bla-,,'- -it
130 - 1.500'-.
elfpct of t~.e ccntent of chan,,-~~!
blac'~.- c.-, zj~a%,-es 1.
in the str)n~th of vulcanisates lurInt_
Card 3/6 aSeln- -t 150 It was also fount that fillers such
as lamp bla-.'~, po~,--Iered sll'~oa E-el and cl-.ai~c do not ~-zffe-t
tV~e 11-1- a-it h --,t L
( -L e - a! e n o ' tu t-l T-ibber. Tests

SOV/138-58-12-2/17
Butyl Rubber. PT I idle 3 1 2,,~, r--;, I ~1 'I n- "', fe C t 1 "e it i0 !~,Z3
Rubber ~,Iixttires
also t`e of siiniij -.t r-.tliji~ion on
but7l rubber on SKB T,,')*_)er. Under analw ous con-
ditior,3, In JDI v-1icanis-toj st-ructur-al i,!-,an~ 1?1~ Cr)llid
be ob.,:-r-,rel 3hovie 1 tliemselves in a Irl"Y --asp
In thin !, Li -ic "ease of the relative elonCa-
V w,
tioll frcm 3~,O Inum ovalwtl,lr~_ 1,1if., el'Ccof. of
flll,.,r:3 on t ,-,- stabUity, the pro~e:j. or ozone
destruction 13 alac to be taken into A small
quantity of ;,.r~'Lcn ':black (up to S,D') ma'ces I'Ll possible
to ':-.,rejLse t~-.? a, :,hich rupture ociurfl, by 100/0
at, , onl-en of -,)2one. Finely-diLipersel white
fillars also resist-in-e t,) 3CeinL by ozone
ol t;jq rui ifli.iates. Thc. fillers also '~~,e proper-
ties ~~' a~'-heqi)n )f .-.F. vulcanisal-S (T~')l.,, `e .,ond
S'-rerztl- of the fl')r.~ , In '-)ut, 1 rubber is '" luo 3 tlm,~s
"an Ir 6F,-E. sicn is 1&3~,; aff;~7-_eJ b- t-,he
a-11 fas a-1 lard ljla~`. The
'e
ir- T`,~.n,ontulnirk 'iliv-3 arc " :j
Is
graph i e -)C1 a:~ ~ie "nI cla'SL
r ~ IL L.,
Card 4/6 f 1b rl- Tnc. b'3 Incr~_-sed !-y varjous a.--i-

SOV/138-5ts-12-2/17
'
c::
Effec"ve
4 le
Rubber. Pr
Bi~ tyl

-c tLl re - .
Rubber -J-

0
F
-
~
-
-In
t:-,e opc,--.'Ide r,
sr -I
, a i z~in 1`1n.101

ol,-i c ro'i I ll
p -I a6
4) Ion
l to du~rc A3e the
i
i
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er 1 -
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(f amate. :..e
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SOV/138-58-12-2/17
D-)- -.-l Zffer,..'ve Jompc3 -, 1,;,,3
-7 IL u re L
of jjiCuient.n 1, !-,e ~;Ide,l ~o the ; lv.tires.
There are 4 Tablf~s, 4 FL,,ures ~I,,,d ra Referer.~es:
Er,r lls,, L!A 4 .)c),
Card 6/6

L f.,
, A " "-' I ~ , " C~
'A R " I f I -
I
-, ~ "'.. -1
I .V
:~ --7'

MUM. g" M 1
DY)CHITS, S.A.; BIIP~IKP S.M. YA16iiINA, Ye, P.; OR ANA
77M3,~?,OV, S.S.; BRCY-KARR-W, G.1 .
Fvtontial aon.ent, of water E,,- Iubla phenolv
tar ii-rid the optimal con,~It'orif~ for thel !- -ippar;i, acr.,
no.1 102~108 1 h,

KULIOVY A'I.; KURLINA, I.F.; POLYAKOAI, I.I.I.; SHIPINOV, 1:.A.;
ZEI;;~"' 1".I.; FEGFILOV, Ye.Ye,.; GAJR!7CVS"-:AD., G.R. [deceased];
PARSIMIA, Ye.P.
Utilization of shale and coal phenols for the synthesis of
chemicals for plant protection., aim. i tekh. gor. slan. I
prod. ikh perer. no.8:152-158 160. (MIRA 15:2)
1. Vaesoyuznyy institut zashchity rasteniy i Vsesoyuznyy institut
po pererabotke slantsev.
(Fhenols)
(Plants, Protaction of,

FFOFILCV. Ye.Ye.- GATICVSKAYA, G.N.; PARSHINA, YO,P.
Re7!~,very cf alkFtli 'rc!- aalt soll~tions efttr t~,p 'lor c'
T-,~,nolaloB. Trldd7 VNIIPS nc.1;:2L.;--2?2 "~ r, .
(Alkalies .) (Phenols ) (011 shal~-s)

YEDFIIA)V, T.Ye.; GAI?I;OVMYA, G.N.; PARSHINA, Ye.P.
Chemical composition of pir-nols in the intertediate tar fraction
from the semicoking of Ba'tic oil shales. Trudy VNIIPS no.4:
205-217 155. (14lu 1~:Z,)
(Oil sialas) (Phenols)

SWENOVVS.S.; DYMSHITSY S.A.; BITUK, S.M.; PARSHINA, Ye.P.; ORIDVA, N.S.
Potential phenol content of shale oil from se-micoking of shaleB
at the "Slantsy" combint. Trudy VNIIT no.10;166-174 161 ~MIRA 15:3)
(Shale oils)(Phenols)

GARNOVSKAYA, G.H. - V,
w Ye. Ye.
Removal of neutral oila and sulfur :ompounds from PhenOlB.
T'rud7 IMM no.7,237-246 '59. (MIRA 12:9)
(Oil stmleo) (Phonole)

GARNOVSUY.A. G.N. (deceased); KUL1KOV, A.I.; 1WRLINA, I.P.;
PARSHINA., Ye.P.; FRffS, H.O.; FEOYILOV, Te.7e.
Synthesis of the preparation 125 from phenols of tare produced by
semicolcing of Baltic shales and Chereml:hovo coals. Khim.
i tekh. gor. slan. i prod. Jkh perer. no.8-O&IS5 160.
. (MIRA 15:2)
1. laboratoriya pererabotki Bmoly Vooooyusnogo nauclino-iselodo-
vatel'skogo instituta po pererabotke slantsev i laboratoriya
organicheskoy khimii Vsesoytiznogo instituta, zashchity
rasteniy.
(Pesticides)
(Phenols)

d

..7"1 9 ez-61L U7
. . ` - s aA
I . .. . ~: - * E; -1 - I - - 9 - '~-, ~ C 7 -~ - - - UT TOU I
:. I I il : ',:,, "; 1. '1""m 'I -. *,]-;;~, I , 1, ~j Ij - ~, "; " ~'L t~ ',,- 2u T UT ja ..,
. I
."." Iv" I,. . .,;. I , . I
. . I . I ! . I ~ . I -il--,;,k ', ' ' A' 01, ' VAO'All:-IH'3,TIIJ

_7.,S7
SUVOROT. N.1.: FARSHINA, Z.S.
H,Tpothesis of the palsobotany of' Kars. Test.AN Xazakh.SSR 11 no.4-.
98-102 Ap 154. (KLRA 7:5)
Predetavleno deyetvitellnvm chlenom Akademii nauk XasSSR G.A.Tikhovym.
(Rare (Planet)) (Plurality of worlds) (Paleobotany)

SUVOIRDV, N.I.; PARSHINA. Z.S.
Spectropbotormtric study of chlorophyll absorption line In
connection with the problem of cosmic erolution of the
photosynthesis. Trudy Sekt. astrobot. AN Ka2akb.SSR 3:33-47
155. (MLRA 9:12)
(Photosynthesis) (Mare (Planet))

PARSHINA. Z.S.
Blogenstic variability of the absorption band of chloroph.711 in iignar
plants. Trudy Sakt. astr9bot. AN Kazakh. SSR 5:221-227 '57.
(Chlorophyll) (Photosynthesis) (MLRA 10:6)
(LeaveB--Spectra)

All

I I
t

USSR/Mysiology of Plants - Photocynthesirl
Abs Jour 11cf 71aur - Biol., Nu 15, 1958, 67739
Autlior Parshina, Z.S,
Inst Academy of Sciences KazSSR.
Title Biogenetic Variabil~'.ty of tho Ckilarophyll ibsorptir)n
Belt in Higher Plants.
Orig Pub Tr. Scktora astrobotaii, AIT KnzSSR, 1957, 5, 221-227.
Abstract Usin,,.* the photospectrometry method, a atudy was rinde ol' th e
basic chlorophyll absorpticni belt in plants at various sta-
ges of evolution, and also u6ing leaves of different aCes.
Species of older derivation assimilated relatively less
light energy -- principlaly red rays in the 666-689 '-~
area. In plants of pbilogenctically young species tic cur-
ver, of lie~it absoxI)tion by chlorophyll slanted wro, iii the
600-700 section; in addition to red rays, thcy also
Card 1/2

'1~11111 ".S.
,~- -a
Philogenetic charactnrietici3 of spoctral brightnoso of plants In
leflected ra7n. Trudy Sekt.astrobot. LN Kazak-h.SSR 6:N~-140
o
I 5R. OERA 11:12)
(PInnts-3pectra)

PARSFINA, Z. S., CandJrlnt- of ',91cl Fri (rllrn) -- "71ne sp,vtj-aj rjjQ-j~.~~ -)f T-I~rjrtr , I
various rysti3matir. j~rmq)F". lt~ TYP (Kazilk-h - 1- '~'. V..
150 copies (KL, No 2--, 1?)
L

GORMM)VA. G.S.; PARSHINA, Z.S.; HUMMO. V.P.
Optical properties and photasynthesie of some cultivated and wild
plants as related to ecological comiltIons. Z.-ady Sekt. astrobot.
AN Kazakh. SSR 8:31-45 160. (MIRA 13:12)
(Plants--Crptical properties)
(PhotosynthesiB)

- : , , 'TI
N i:rlfl', F , , . I , , : . , , . , ) . I . I . . - I ,, , ,
1 - - ~l - , , ,, . I . .. , I .
, f I - I .! ! . I ; 4 '1 , . , " .. , "' , ~ : I , -, - . . I
tic . - ': . 1 .1 11 1 ;~ 6 1 1 .

YA-KOVL.7VA, Z. A., RUBAN, 1. ~. ; i ' -'~ -,
DryLng of g~by -.!-, a -x - ----Y,)7, . -1dy k: ~ne 7ni ro
0
no. 2 lz 3t>-.,,) It ~ , ( m T u I - ~ 8 )

--TARSHMSLU-, V.A.
Digital device for progra=yzing the machining of sections of
simplest surfaces. Sbor.rab,,po vopolektromakh. no.7j250-261
162. (KIRA 1631~
(Machine tools-Numerical control) (Automatic control

t 34o69-66 ME d) I OKF( I) IJP(c) /B
ACC NR& AP6019780 SOURCE CODEt UR/0119/66/000/006/0016/0017
AUTHORs Parshinakiy, V. A.-(Engineer)
ORG: none
i TITLEi A continuous digital Integrator using ferrite-trangintor elemenLs
SOURCE; Priborostroyeniye. no. 6, 1966, 16-17
TOPIC TAGSt digital computer , transictor, comiAlter component
ABSTRACTs A digital integrator using ferrite-transistor modules is
'shown in the figure. The unit is basically a binary multiplier per-
I forming this function by AND, OR, and INHIBIT logic operations. As
iseen from the figure, the unit contains k (k-integrand bit length)
dynnmic flip-flops. each consisting of 4 ferrite-transistor cells. The
!cell with a constant magnetization in performs the delay function; Lite
~output cell is an INHIBIT gate. The register consists of a k seriallv
connected row of static flip-flops (To - Tk-1) forming a reversible
binary counter. Switcliing from addition to subtraction mode is done
by a transiscor flip-flop T3il,, Counting pulses from the frequency
I divider (TO - Tk-1 tatic flip flop column) are applied to diagonal
a
,dynamic flip-flop inputs. The synchronization ie performed by a 6-stage
i CQrd 113 -----.-U DC: 68-1-.142.644.3-

L 34069-66
ACC NR: AP6019780
Fig.l. A continuous digital
integrator
,ring shift register driven by a two-phatie pulse generator PG. The
,schematic diagram of the static ferrite--transistor flip-flop is given.
,It performs reliably in a temperature environment extending from -10 to
+60C with input pulse train repetition frequency up to 120kc. The
pulse generator is also shown. It has a relaxation oscillator stare
and a buffer stage. The row of flip-flops is initially prepared by
application of pulses on their 0 and I inputs. The initial value of the
integrand is introduced into the register in parallel form. The PG is
activated and integration proceeds in 3 stepst 1) a pulse in applied
Card 2 / 3

1, 34069-66
ACC NR: AP6019780
to the independent variable terminal 6x; the counting pulse frorn the
frequency divider flip-flops, which change states from 0 to 1, rends
out the information from the corresponding cell. thus forming a Ix
,output; 2) next a 1 is rewritten into the cell which reintroduces the
original code combination; and 3) a pulse Ay (representing an incre-
mental Integrand change) is applied to the terminal marked &y. The
integrator output only appears during each first step in a series of
~the 3 step iteration process. Orig. art. hast 3 figures. JBD)
SUB CODE: 09/ SUBM DATE: none/ ORIG REF: 001/ OTH REF: 001/
ATD PRESS:
C d 3 / 3_

FARSHIMM, V~A,
Investigating and deaIgning a tize-pilBe multiplier. PrIboro:31.rjrvjiP
no.4-.1&--12 Ap 162. OID~ i I /.,
(Electronic analog computers)

FARSHINSKIT, V.A., mladshiy nauchnyy sotrudnik
FrequenC7 characteristics of DATs-50 point-t7pe arc lazes. Zc--,~'~;-
tekhnika 6 no.7:11-11 Jl 160. (IAIRA 13:')
(Electric lamps, krc)
(Telecommunication)

PAIIID!'77-71, Yu.A.; , (s :: ~ .
S(,C.,., ~ - , .- --. ~ V ".. -
. . : . ~ -7- S - - .. 1 , -*:- P.., --,a ~ - .:,
S, ~ 1, - t . I.: -. . :e' o '.- .1 . '. :( , -1 P. , 1-1.4. 1, , /- --. ~ .:, ,

GUSENKOV, A.P. (Moak-va)-, PARS H INTS FVA, T.S. (Hoslrva); SluiMIROVICII, R.H.
(Most-va)
Some characteristics of repeated-strain uurveB in case of a synnetrical
stress cycle. Izv.AN SSSR. Ctd.tekh.naak.Mvkh.1 mnshinostr. no.5:108-
112 S-0 160. (MIRA 13:9)
(Strains and stresspe)

LINIKOV, I.M., kand. tekhn, nau&; Prinimal& uchastlYe P-05HINTSEVA, V.A.,
starshly tekhnik
Tests comim-ted with wall
asbestos cemont coverings.
(Asbestos cement--Testing)
r)anelo Vith a wooden framework and
Trudy TSNIISK no.26:5--41 '63.-
(KUIA 16:8)
(Walls)

PAR5HKUV, A.A. I- inzil.
Surveying inBtrwat.-ntB for railroad surveyim. 'rudy IdMil
ao.30:23-28 162. (1-URA 1c,-.9)
1. Sibgiprotaii!~.

ACC NR% AP70001407 SOURCL CODL- Ult/0413/56/000/021/0109/0109
INVENTOR: Clietverikov, A. F.; Pashkov, A. B.; Samborskiy, 1. V.; Grachev, L. L.
ORG; none
TI','LE: Preparative rwtilod for polywrs con:ainirig anthraquinme redox groups.
Class 39, \o. 187999 (announced by Scicritif',c Research Institlite of Pla6tics
Miuclino-issle6ovatel'skiy illstlLUL jilastidlelkikil Man~i)j
SOURCE : lzobreioniya, promysalennyye oibraz:.sy, rovaril)ye zna~i, no. 21, lljoc,, v-.t
TO':C -,ACS: ruc~ox polXn)er, polyviriy;a1hr,,qui,i,,Mc /,1-4, (-1
ABST RACT: An Auiior Certificate nas been ;~.suu6 for a )repara~-ive i:a2'Li,o,~
po:v-,,,,c-,s corlainii,,~ anLhra(;u:nunv re~:cix lhascu oil styreiie 1.1(, 6,V ';I .......
A sty rone-Giviny L),,nzene C-On,0lYl-.W r 1S L rl~ ~11 C6 Wt i1 111'1,y ~lr i UL' 1 i1
solv,~,-,z in pr-,~6ence of an cxccs~, oz - c;iiori(iu, and LNC -,CLU~~Iltg
vinyl6cr,zoylbenzoic acia -~s conve,-teo to y treaLiaci-it
poiyv~nyiat~-ra~uinoiie
su~lurkc acl 'd or oleklm.
S'L':3 07, ii/ o-",7L. A,-,)
Co -d (, 2 3. 2 o. 22

AGO ~a: AR60291174 SO:,aC-- CODE:
iOR; SI-or, A. M.; Parshukov, B. A.; Mtsanova, A. L.; Churk'n, V. S.
UTI I I
TITIE: Eddy-current 'Loss in printed condactors of electric-machine windings
SOURCE: Ref. zh. Elektronika i energetika, Abs. 6166
RET SOITROE: Sb. dok'. k Na-,~chno-tekhn. konferents1i po electr. mash-nam s pac~,atr-
obmotkami. Novosibirsk, 1965, 56-70
TOP:O ?AGS: electric machine, qinted wi.%diLng, eddy current loss
J
have been developu,07Lor dote.-:aan-.ng t~e eddy-current loss n
prir,ted-w-_*__.-..- conductors, in d1sk-type and cylincric~` c-c machLne5. AL `--st, a
curve of ma7natic induction in the inter.Pole space ~'which esgent-.ally G.ffers
fron. the straight line) has been plotted by using t.,,,e method of conformal
trar.5for-mation and also experimental data. 7he losf;es are calc~latea on a
d'_critai computer for various dimension rat'.os of the magnotic system. in LI-le case
of disk armature, the loss was determinei in copper-foll segments pasted on a disk
which was rotated In a magnetic field by an auxiliary motor at a constant rpm.
The losses were calculated from the brakcin,g torque measurod by a spring-type
Card 1/2 UM 1 621. 313. 1

ACC NRi J,,TjuO29473 SOjRCE CODE: UR/0196/66/000/006/1010/:010
A',T~iOR: Shor, A. M.; i",atsanova, A. '-.; Parshukov, B. A.
TITLE,: Distribution of eddy-curront loss ~`ong the prLnted-.11nding conductor ~x, a d-c
machine armature
SOURCE: Ref. zh. Elektronika i energeti