SCIENTIFIC ABSTRACT ZAIKIN, YE. - ZAIKOV, R.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001963430002-3
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: March 15, 2001
• Sequence Number: 2
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

- - - -------
ACG IIR t
AP6021781
Fig. 1. 1 - narrow-band filter; 2 phase dotoctor;
3 - amplifier; 4 summator; 5 - low fre-
7
quoncy-filtor;_ 6 balanced modulator;
7 - phaso ohifter; 8 amplifior;-
9 - amplitudo dotoctor; M- low froquency.
filtor
Orig. art. has: 1 diagram.
SUB GODEs 09/ SUBH D=: .'22Ja65
Card 2/2

SMIRHOVp G., podpolkovnik; ZAIKIN,, Ye., myqr
- '! -T,*-;. r, - ..
An air regiment retaMs conquered heights. Komm. VooruLf,
Sil 4 noolls37-45 Je 064. (Hill. 17sq)

DONWARIV) Y,T., 1:arid. tekim- nauk; MOAKOV, V*Ao p lnzh.; MKIIIAO A.A.,, Iml,
Friv,--t;Ugating th,o composition and the nature sf chemio&L heterogenelties
In industrial glazso Stek, I kero 22 no.8:13-15 Ag 165. (MIRA 18t9)
1. Zavod IlAvtosteklotto

K,T.~ MINAKC113, -11AILF-1111A. A-A-
164
Q Nn r~: T--i

11;oo "I
ZADLINA, 1. 11. CsLnd Agr Soi -~. (dies) "Selection of maple trees umlar oon&tLons
.t4We-,A -
-LAI)
of Moskovskaya OblaLste Voronerh,'%'1959. 20 pp (Min of Agr ISPBR. Voronesh
Forestry Lngineering Inst), 150 copies (KL, 49-59, 141)
_68-

Hotbods of produaing large-grained millet formp. Trudy 101P.
OW,biol, 5t164-172 t62, (KmA l6 t 5)
1. Mavn" botanicheakiy sad AN SSSRp Moskva*
(MILLET) (COWHICUS) (POLYPLOIDY)

viph; m%LSROVICH. Anna yefluovnel
..yUCHIKOV, Valentin NikO1870
red.
Eps alysis) Paralichi* IAroslavl, TAroolavokOG knishnos "d
r
1958. 87 P.
(PARALYSIS)

ZAIKIN Veni inzh.; OBFAZTSOV, Vnevolod Vladimirovichp
-I.tekhn.nauk.. dotBent
Special features of the eynthesis. of multicyole relay systems
with contactless asynchronous elemen's. rzv.vYs.ucheb.zav.
elektromakh. 7 no,l2tl470-1474 164. IMIRA 18:2)
1. Gidrofizichaskly Inutitut Ali McrSSR (for Zaikin). 2. Kafed~-a
avtomatiki i telemakhaniki, Novochorkasakogo politekhnichaskogo
instituta (for Obrastsov).

Ye.Vq UaTNA.
VYGOVt
UnIng- of hatrth blnckss~
ph aea trca 6fr,-:~~at ~,7, am--rtzits-
164.

M
ZATKTVA, Y. G-
X^d. IWt-, -c191.9-
Nor., In3t. Phy3iological ixa. L F. Favlov, LI-pt. Biol. Sci., Accd. Zci.,
"The Problem of Efferential Functic-mi of thin Dorsal florve:s: I. Fc,le of tho
Ir!rv6s in Snmphathttic Crbcli-Gine Tsinnkiy Phenotiena in f;,01d Blocclei
Dorn ~3 111
I~ni-nals," Fiziol. Zhnar. SSSR, 35, No. 191+9;
d...Ii. Effect of Do-rial Mnrvez on tht -of 3~.m. -.alhelti-_ Cr:),.k11
Ginetstnskiy Phenor.!tna in Itlarm-Blooded Animals," ibid.

r= MR". -
38290 ZAIKINA, M. T.
Vllyaniye ezerim i atsetilkholina na siq*ticheakiy fe:aomn orbeli-
Ginetainakogo. Sbornik trudov (Arkhang. gos. med. In-t)p v7p, 91, 191.90
s. W-23. - Bibliogrt 16 nazv

YELIKOV, 9,p.) ZAIKINAJ,~ IAIIA.
--j
Some properties of Cell Oxtracte frm y"st ftngi. Blulokv-
biol, i x6do 59 no.598244 065, (VI RA. 3.8: 11)
1. lAningradskiy khimiko-fm'Mt8svtich89kiY 'nstltut' j,,imitted
February 4p 1964.

YFLIfiCFV,, N.P.; FROLOVAj, M.A,; ZAIKINA, N.A.
characteristics of the complem-ant fixation reaction in nandidlasis
ta-eated Oy antibiotics and other preparations. Eksp, klin. lssl,,
'Xim 1525)
po antibiot. 2:UG.U5 160.
OLEY
(COI LENT FIXATION) (MONILIASIS)
WrIBIOTICS)

-QpmAlr.MaW4
V. V. DOBRC),"ffSLOV V,V.; YELIWOV~, N.F.; ZAIXIIIA, N. KOIIDRATIYIVA,
BYSTROVA A*,,
A.A.; MXDVEDIKOVA, A.A.i SILUYAJIOVAP N.A.; MVX -0--9-T,
Study-of the antifuzigal propertiesand chemotherapautle. actirity of
antibiotio 26/1. Mcsp. i klin. ioul.-po-antibiots 2:2t~-~-295 160o
(FIRA 15:5)
-(ATITIBIOT.IGS)

YELINOVS N, F. ; Z A I KI 11 N.
I'll"ido,
Vor.. med. 9

F7,-!T ( 1, /T .;r
AR6022387 (N) SOURCE CODE: UR/01197/65/000/024/6065/W65
ATjTHOR: Felldman, I Kh,; Frankovskly,, Ch. 3 Yamshchikov, Vo P.;
-Mordvlnovep Yes To; knryukbtap Yue &; Zalkinap.N.-46; Vito-rokays, G. o;
Arkad'yevap 0, Ye,
TITLE: Azo-derivatives of benzene as potential antlbsotqrial~compounde*
SOURCE: Ref. zb. Formakologiya. Toksikologlye, Abs. 24-54-512
REF SOURCE: Tr. LeIningr, khim.-farmatsevt, vyp. 18, 1965o 171-17
TOPIC TAGS: benzene, chemical compounds rlicroorganism contaminations
bacteria,, plant parasite
~ABSTRACTI An In vitro method of serial dilutions was used to test the
activity of several syntbatic azo-compounds in relation to
dermatophytess some gram positive and gram negative bacteria and two
species of yeastlike molds. All the tested szo-compoundJ containing a
carboxylic group proved inactive. The exception was 2.4-dichlor-3-
carboxy-41-oxyazobanzolo The azo-compounds displayed highest activity
in relation to Cro.nooformanap weaker activity in relation to
dermatophytes* and the weakest in relation,to Candida. albioans, Only
L c6rd lZ2

A.C NR- AR6022387
certain azo-compounda displayed antibe2aterial and antIvIrus action* The
bigbe3t In vitro activity was displayed by 2.4-dieblor-41-mothyl-4-
oxyazobenzol and 2p4-dichlor-41-oxyazobenzol which proved most effective
in relation to yeastlike molds and dermatophytes.ond weakest in relation
to bacteria, No Zabolotakayao 47ranslation of abstrac-t7o
SUB CODE: 06,p 07
2/2
card
L

ZAIKINA, !.A.; YELINOV, N.P.; YAKIWVt P.A.
Purifleation of waste waters Ar-the antAblotics industry. -Trudy
Len,khim.-farm,inat, no-15t279-284 162. (MIRA 15;11)
(ANTIBIOTICS) (lNULbTRIAl, WASTFS)

~,-ZAIKINA-, N.A.-
Tojeting the nev ant(fungal antibiotic 26/1 an the CdMU& carrier
state in white mice. Zxop. 1 L-1-4-n. isol. po antiblot. ;Zs296-299
160, (MIRA 1515)
(CANDITA) (ANIBIOTICS)

ZLIXIYA, M.G., kand-fiz,ko-matematicheekM nauk
3brpansion of eTen numbers of an imaginary quadratic field into
- a sum of tvo Osemislople, summands* Veh. cap. Kalin. goo. peA.
inst. no,5:88-117 158a (1KIP-413:10)
(lumbers. Theorv of)

I ~ IU.111VA. N.G. ~jnxry quadrstic field ConsistlAff
. --1- - ..- " ~-. I - i, i1i of wobers of au 12N I
-- itriblat deals. Vah. Ica? HDPI 108, 261-272 - '."?- (Ku 11112)
-1 f Small simple i
(1,=-ooro. Theorf Of)

ZAIKINA N.O.
'Matribution of nonresidues of the power a along ths,:xodulus of
,simple ideal In an Iroginar7 quadratio flold. Vch.-%xp JGPI 10&.
273-;2E2 157, (MIRA Ili 12)
(lumbers, Theor7 of)

I I ZIMINA, N,G. ---- the soutYArn
t ta 0 ic f.,jorj f'ro,% Quaternary rjedirAnts af
digtor -
pal,t of the maz Poninsula. Vesr, Mosk. -an. Sor. 5i Geo 19
A ~kRA 17:4)
nc.l.-76-78 Ja-F 164.

IdZSBINSKAYA, Z.V.; ZAI IIA MIRE, A.P., doktor geogr.
;Kl~
nauk,, red.
(Guidebook for practical exercises in a course on
"Quaternary geology"; method of diatom analysis] Ruko-
vodstvo k prakticheskim zaniatilam po kur--u "Chetvertich-
naia geologlia"; wtod diatorovogo analiza. Voskvap
Eosk,, gos, univ., 1964. 74 P* (KIRA -18:5)

ftEvi-i-U-aIti-en s of Munerical Irimcticus Conn6eted-Vith Swe Problems -in the Theary
of Mraginary Quadratic Fields." Cand Pbys4kth Salt Moscow State Pelagogical xr-stp
Moscov, 1953. (RZWAtv Jan 55)
Survey of Scientific and Technical Diesertaticas Defended at USSR Higher
Educaticnal Instiutions (12)
SOt Sm. No. 556, 24 Jun 55

MKINA, R.O. (Kiyev, ul. Sakmaganskogo, d. 83, kv. 1); VOYSTATSMY, V.A. (Yiyev,
'---------uT.-Chudnovskogo, d. 19, k-r. 12)
Distribution of ethylene-substit-ated phosphoramines in c4irtain tiestAs
and o-gans of animals, Top* o&c. 4 no*$.'557-561 158. (IIIAL 12:1)
1 Iz ukrainskogo nauchno-issledovatel'skogo sanitarno-IdAzicheakcgo
I;stituta (dir. - dots. 11.1. biganskiy).
(CYTOTOXIC DR=, metabolism
b is (1-az ir idlayl)-phany lamina phosphina oxIda, distrilution
in variwis organs In animals (1ha))

Work capacity of hyprtenaive patients before ej~d aftir treat-
ment with RwMolfia proparations in -a polyclinic. gov,aosde 26
no.112104-107 11162 (IMA :L713)
11. Iz polikliniki imeni Dzarzhinskogo (gl&w,yy wach -- im-
oluzhemyy vrach PSFSR T.G. Karakozzorv zave terapevti.-fteakim ot-
deloniy(im B.A.Abanenov)p W)vkvao

ZANDW, T.A.
Atheroaclaro-tic-c ardlos clarosts vItlwut hypertension wid with It.
Sbor,nauch.-prak.rab.Poliklin.1m.F.E.Dzersho ao.209-44' 161.
(MIU 1614)
(HEART-DISEASES) (HYPERTEISION) (ARTERIOSCLERNIVS)

ZAINIM, T#A#
I
Treatment of ,"artension tV xms of Rawolfla serpent:40
. preparations In polyalluics. Sbor.nauch,,-prsk.rab,FblUUn.
im,F,E.D%Grzh, no,245-52 l6le (MRk 164)
(HrMTENSION) (RAUWOLFIA)

BAUNNOT, A., lush.; ZAIKIN&* V., Insh.; IPPOLIWTA, I., Insh.
Devica for erecting reinforced concrete columm. 1k awrol.,
Hosk. 2 -n0-8:30 Ag 159. (MIRA 12:.,:L2)
1. Stroitallnyy uchastok-19 tresta Roastroy 96.4.
(Coluxtas. concrete)

SUCHOGLO.VP -81.I.;_~~~V-,'D-*
Effect of technolo~gical factors on the comwtlw - of rwor fap- - I --
sterite materials, Ogneupory 26 no*7;323-327 163.012U 16:9)
L, Dnepropetrovskiy metallurgichaskiy inatitut,

3/137/61/000/lDll/008/123
A0601AI01
AUTHOR: Zaikina, V. D.
TITLE; On the problem of slag-stability of fireproof articles
PERIODICAL- Referativnyy zhurnal, Metallurgiya, no. 11, 1961, 2. abatract UB12
(113b. nauchn. tr. Dnepropetr, metallurg. In-t1f, 1959, no. 38,-85-90)-
The best resistance at high temperatures and low slag Witions was
demonstrated by Dinas brick and dense forsterite in the study of refractory-slag
eq:jilibrium systems., At low temperatures and high slag additions the forsterite
chamotte refractories have In all instances demonstrated a low duratility. The
greatest destruction was undergone by Dinas.refractory and by porout synthetic
forsterite on account of the formation of 1o% melting-point silicatca. Forstezite
refractories, in contradistinction to DInas brlck ones, form with the slags an
easily removed crust. Chamotte refractory i~i destroyed on account of the inter-
action of the slag with the surface of the r(ifractory and the runof:.' of the
reaction products from it. The greatest durability was shown by ma4pesitochrotaite
refractory, dunite forsterite, and dense synthetic forsterite. The nature of
their destruction Is: magnesitochromite and the dunite forsterite are
Card 1/2

S/13 7/6 1 /ooc)/o 11/00 8/12---'
On the-problem of-slag stability-,.... AoO/Aioi -
impregnated with. slag, -and the dense -synthetic- forsterite is destroyed as a-
result of corrosion, dissolution, and slag-saturation.
V. Oparyshevc
[Abstracter's note: Complete translation]
Card 2/2

WSR/gngibaering Pover Plants, S&P ~q
Electric
Engineers, Pover
*Kiev Interoblast, ]Department or VNI= (All-Tinion,
Technical Society of Power Engineers)," A A.
1p- Wko, Engr, 1 2/4 pp
'Slektrichestvo" No 9
Oml the basis of results in socialistic cow-
Petition of VNIM departments, Kiev Interoblast
Dept vas awr-rded first prize and transferable Red
Sumer for 1948. Contributing factors in the
11ev wacce as: (1) mass participation of society
anabars in cnative I scieAtific fng"
'64ie --r='n%'xp Slibetr e'L
(ContdY
activities, rendering aid in orgeanizational and
Acientific engineering matters for improving qualift~
ettiona and expanding political vlevpoints; (2)
originating measires to strengthen creative teawvork
*f scientific and industrial vorlters, emphasizing .
liv=tance of new techniques.; (3) aiding innovators
sad efficiency experts of Industry. The Kiev society
bas nearly 700 members.

77'
USSR/Ilectricity Personalities Mov 51
wP-rafes-e-or-A.-T.- Orlovskly (HIs--50th-BIrthUy arA-24 Years-of Pedapirical- cad Public
ActivitA" Prof A. D. Mesterenkos Corr Rem, Acad Sci Ukrainian SSR, !?~rof 1. 1. G-.!GberLl
Dr Tech Set, Docent V. G. Xholmekiy, Cand Tech Set. X. V, Zubanov, C'hLef Inr . XLeven-
ergo, Yu. V. Kartashavokly. Chief Znf-r. GI-mve:-targo, RM, Ukrainian STR, A. S. Taretsov,
Dir, Kiev Heat and Pow*r Sta. A. A. Zayka, Ingr
"Ilsk-trichestvO No 11, P 91
Orlovskiy has been he" of the Cbni.r of Centr&I Zlea Power stations, Kiev Polytech Inst
since 1937, and Dean of the Mec Ragineering Taculty of the latter Institute since 1944.
At present. he La directing work in the Kiev Polytech Inst on the problem of generating
reactive power in mercury-converter units. Orlovakiy has trained more than 1,500 eloo
engineers*
201TO

I-- ---I ','a-w'
Mr R.4,
A., ZAVSSKIY, A0 M., lSktOY. V. P., vismmy, B. A.~
SRI-',RBTN, S. M., AMTJSCFLISKIY. F. K., BAUPGOL'TS, A. I.,
ZO,WTAIV,V, T. L., PUSHIMEV, M. I., PROSMYAKM V-, GURVICH. A. H..
~F'SIMO, A. I., SHM-S, 7.'T., XONMATIM, G. H., IMOV. S. V.,
ALUS74M, A. TN., BOLOTOV. V. V., TMOIE M-, 1. M., GERASIKOV, 5. T.,
MONTI M, I L. A.. LMVIT,- GO. O.,-ORLOYSKIY, A. V., VZDIUiOV, V. M.,
STRIKOVICH, M. A., GIMMAM, L. K., NIKIYOBbV,- V. V., SOLODOMKOV, 0. S.,
SMIRNOV, S. P., ZOLOTA"WA,N. A., KALXXIITA, -9. H.. GOLIDICRSUZZYN, T. L.,
XTEBAROV, L. D., SALUYEV. N. F., ZAIKO, 4. AUL.MARIMS, H. F.
A. S. ObituAry. Maktriabastvo, No. 2, 1952.
SOI - Month List Of Russi8n ACCessionsp Library of congress, Tml,,r 1952 Una.

ZAIKO, M., inzh.-pilot
I
Can weather be ordored? Grazhd.av. 20 no.11:22-23 N 63.
(MIRA 17:2)

RAZADVI A. T#~ and H MjIACIT2VAp`Oo A. S. . M. RATov chor"'Icrij.
Tcchnolor!,icnl Inotitutc, Kazzin, and the K--ziii ll-~iccnl lrztitutc)
"Estcr3 of fdl~ylplhosphoncus ard Dioll-Ilphosphinic Acids and Thei~- Bio-
losicijl Activity," Kbimiva -4 Premencenic Socdinerii
(Che-mistrly and Applicotions of Grgaroplicspharous C=p,:-unds) pp 205-217, 1c"57
fl*)O: A-3MI, fWl trv!wl.,9t!or.

AMSKATAo L.8,; Urim=A, I.Y.
Pharmacology of the paranitr*phwql aster of diethylphotqihorle acid
[with summaz7 In English]. Pam. I toks. 22 no 1:66-69 "'~-P 159.
(HDU 12:4)
1. lafedra famakologii (zav. - dots. ROA. Aluf) Xazanektgo madi-
tainalcogo inatitata*'
(PROSPHINIC ACID, role cpda.
diethylphos Inic acid p-nitrophonyl aster.
pharmacol. Rug))

ZAIXONHIK(YVAt
Nibuphinq a nev cholinamlwtic drug. Faz. zed. zhura not 2:41-43
Mr --Ap 163. (11MA 14-4)
1, Kafadra farma,',-olcgii-(zav,-- dotsent T*V. Raspopova) lizanskogo
maditainakogo.instituta,
(PHOSPHINIC ACID)

VLASNOVAI V.M..; ZAIIM41UNU-~V'
flibuphinp a new antiglauccmatous drug, lUtz. =ad. zhur, =). 2:46-48
Mr-Ap 161. (I-ILRA 14:4)
1. Kafedra farmakologii (zav. - doteent T.V. Raspopova) Kizanskogo
meditsinskogo instituta i kafedra g:Laznykh bolezney (zav. - prof.
A,N, -Kruglov) I Kaza.askogo gosudarstvennogo instituta dlya usovershen-
stvovaniya vrachey im6ni, V.I-.- - IAnins-,-
(GLAUCOMA) (PROSPHINIG ACID)

TONATTEVA, O.A., ZAIKM-IKOVA, I.V.1, AGONSKLYAv L.S.
Antibacterial properties of organic compounds of phosphorus.
arxi - - -
application of organopImpIvrus comicands) &, IV,. AR~3=ir,, Ed,
Publ. by Kazar &MI, Acad, Sei. USSR, Hoscow 1962, 6 1
32
Collection of co =late Papers prosanted at the 1959 Kazan Coaforance on
Chardstry of XganoohosphoruB Comounds.

71. AM- , AM. YITIR CoR.
BIC:PG1 ICU AC'.'!V:':! C, A,D DIA I
4 ?57
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D.Niliu;l) OF TM~ 07 M12 YrC;:, U
. . . . . . . . . . . . . . . . . . . . . 4L3
7A. MICIV V;'.1 6Y
. . . . . . . . . . . . . 4 ~-41
75- Kil =-TA M' O.MANQ~)l
. . . . . . . . . . . . . . . . . . . . . . . 4,;3
76. BICCYI',, AND :MPZ7:,;-, 0, 1 f:,.. m IA 11 'r., W t
',r . . . . . . . . . . . . . . . . . . . 418
77. TJ 5 F.' 0 P. PmoF03 Dvyr ~,, f. OF TAN e.) 1.1 11113 .
V. N. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 472
71), UP, AV M.',Lt :J':; IN -ifS OV kliD I i4Uf;,-MAL
'
I. ~, V. . . . . . . . . . . . . . . . . . . . . . . . .
IU!Z0!-- 47G
79. IXXICo=! OF CIIGAVIIII~~:1141: . . . . . . . . .
60 POLIC.N[M.
. . . . . 4CS
. . . . . . . . . . . . . . . . . . . . . . . .
ff.1,,.,-,*-,I;Y,~,,-!,) JOIN-MT ~XOPO!,
. . . . . . . . . . . . . . . . . . . . . ... 430
62 K.A.
. G,~ 7:- Ac A lii~&IAFAT~,-,:l 17"..
. . . . . . . . . . . . . . . . . . . .
61. CLTNIC-41% V. 14. k;tt~ gm.
E15 D T~, - 0 [ Ii 0 t, G %: 1 A GA C', WXC A. Z. 14. 03!
,
. . . . . . . .
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51Z
87
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TUIC17'-f OF T
. A. 1. Colo,-`-, . . . . . . . . . . . . . . . . . . . . . . . . . sis
ca. Al ir-li SICIZIEZ3 A.M
0 . . . . . . . . . . . . . . . . . . . . . 520
Eig Z~Isz:l CF ON pril 27.~, ",
524
.
of Zdl

clr~~ 't"IL -C,
j

KUDRYAVTSVA, N.P.; ZAIKONNIY.CIA, I.V. ; AM, KCA, L.S,
--
Effectiveness of new phosphorus organic substances in I;Jie
troatmont of diphtho'cime Ir4z *Mod. Zhur. no.6t4l-44 162.
(MIRA 170)
1, Kafedra detskikh infoktsi) ~zav.-prof. N.P. Kudryavtseva) i
kafedra,faravAologll (zav.-dotsont T.V. Raspopova) Kazanskogo
meditsinskogo instituta.

AFONSKAYA,, L,S*; ZAIKOIINIKOIIA,, I.V,; RZHEVSKAYAO O.F.; STUDFANTSOVAp I.A.,
Mechanism of the action of amin and nibufin, Fara. i toks. 26
no.2:184-189 Mr-Ap 163. (KIRA 170)
1. Kafedra farmakologii (zav. - dot-sent T.V. Raspopova)
Kazanskogo gosudarstvennogo meditsinskogo instituta.

AFOIBK"tyA~ ZAIKOI;Lk'I A
love
Search fcr Frote:ctive an! 4 p,J
r
with some cirganopho.-3phonin cof:pmrda. Ratich. tr .y a,,;,. -C n,7
red. in,-t.
1. K&iedna farvinkologii (,,-a%,,. - dot-,ent T.I.'.Ntjpi)j,,:~v
Kazanskojo medl",fFinokogo In.9tituta.

:IDUX.AM. A V G ZAIKONIIIKOVA,-I.v .-
ll!-L ~xeating -'ri-7Jrr,-,-.;7r-.,a2!5 Ir
1. Kafedra farmakologil (-Lav. j
2--Tu kafedra 1
M shcharov) Kazanskofro me it

Pleabanima of Lh" actl~,,r. of -1--ittifir. on I.,- i"vaxt -,7.
acuto radiation. -~i.clalens in 4!d. nid. 9 nc,.2v5C-,:)- 'D 164.
1. Kafodra i rwiielogrli i luitedra farnzdlcl~Np"i
Kazanskogo irieditnln-,lkogc~ Ar-st1ttit-ap

-ZAIKONIIIKOVA,- -I V -, KADYROV,--M *-G~; -YARYGINA, - Go- -
Experimental -- studies. of - the-- harr-,lees nature of epoyy caspoun.da
as a dental filling mterlal. Nauch. trudy Yaz. goo. moil. inst.
14:173-17,4 164- (MIRA 18'.()*,
1. Kafedra terapevtichaskoy stomatologii (zav. - dotsent G.D.
Ovrutskiy) i kafedra, farmakologii (zav. - dotsent T.V.Wkspopova)
Kazanskogo moditsinskogo instituta.

T. V.
Ra=lta of the work of the Niarrviiological Departz~-..nt Iii
study of organophosphorva co:~,jnuracm, I'lauch. trudy
med, inst. 14:175-176 164. . (!,!,T i18:9)
1. Kafedra farmakologit (zav. - dot,Jont T.V.Ravpcq-.ova)
YjA,Umakogo madiuinskogo inotitutao

ARBU,7,()V j B.A., akademik; V12,ELI, A.O.; ZAIKONNIKOVA, IN.; 5RI)EIITSOVA, I.A.;
DTJ','IAXEV, V.G.; ZVEREVA, M.A.;
Oroganophosphorus compounds of low toxicilq-. Dak-I., 1.11 S,3-c7R 265
n0.1291-94 N t65- (MI RA 18: 10)
11, InBtitut organicheskay 1-hi-mii All SSSRI, Fazzan', i Fa:.panskiy
gosudarstvennyy meditsinskly institut.

ZAINONNIKOVA, T.I.
-
14 xican ipeclos of UV ge*us flentzia Tlhunb. &tmt.Gort.. a'-155-161
t630 (MIRA 170)

ZAIKOHHIKCNA T. 1.
of the Bpeciea of the gemm Deutzist Tlvmb. belo&--,
ging to -the oection 14esodautzla Schnaid. Bot.zhur. e,? w.2i2O2--
212 F 162. (HIRA 15:3)
(Deuttla)

ZIAIKOV. AleMandr Matmeov
ZAIKOV, Aleksardr Matveevich. Geroichcskaia 5hatura, pervenets sovetskoi elektrifiEntsii.
Y,oskva, CDsizdat, 1928. 1-19 p.
DLC: MI. ~z"6 - 5148 7,3
SO: LC,fl~viet Gec!graphy, Part 1, 1951, Uncl.

28674
8/92 0/61 /14 0/'002/019/023
Ll $ C)O BI 30/B1 10
JXTHORS: Zaikov, G. I., Mayzue, Z. K., and Emanuel, K. IA. , Corresp()rkd-
Tn-g-M-e-m Fe-r -1-5 _'U S S R
TITLE: Mechanism of chain ramificati one .-during - oxidati on of methyl
-------ethyl ketone in-liquid phase
PERIODICAL: Akademiya nauk SSSR., Doklady, v. 140, no. 2, 1~)61, 405-406
TEXT: The authors found that the degenerate chain ramificatic-n during
oxidation of methyl ethyl-ketone (1) in liquid phase proceeds through the
decomposition into radicals of two intermediate compounds, keto hydro-,
peroxide and diacetyl. (I) was oxidized with atmospheric oxygen in an
autoclave at 50 atm and 100-1450C. The oxidation products (acetic acid,
ethyl acetate, diacetyl, ethanol, peroxides, 00, and C02) were analyzed
chemically or by paper chromatography. Prom the course of the kinetic
curve for the (I) consumption (Fig. 1) it may be concluded that the oxida-
tion is a reaction of the first order. In fact, a complicated process
takes place, which is suggeated by the chain reaction and the itnomalously
low factor before the exponential funottoo in the aquation for the constant
Card 11of

28674
,/61/140/'002/019/023
S/020
Mechanism of chain ramifications ... B130/B110
of the reaotion rate k = 5.2-_1Q,exp(11,200/w) Geo-1. --The chain
---Character -of the~procesa was Froven by addition of a-naphthol-(II) as
inhibitor* In the presence of (II), a noticeable induction period occurej
the duration of which rises with increasing inhibitor concentration. Tne
rate of formation of chains dvring oxidation of (I) gas deterzined from 1<
the kinetics of inhibitor concumption: G)o - 1-5-10- mole/liter-sec at
1450C. During the process, the rate of initiation rises as c:,mpared with
1% due to the formation of degenerate ramifications. Ths rate of
initiation during the reaction was determined by measuring thiB consumpt:Lor.
of inhibi tor (11) freshly supplied at different time interviLla. Fig. 3
shows thi~t the oxidation of (1) proceeds like a chain reactioa. The ra".e
of initiation, however, rises to double its value only~, Fordhe rate W of
oxidation of (I) t it is written down; (j - (k2/"5)1RC 11tji j 12. k11
increasevof the reaction rate (j to-double its value changes the initiation
.rate ci11/2 by the 1-3-fold Ionly, which leada to a linear dependence of the
reaction rate on the-co=entration of (I)p i.a.g to a reaction of the firv:
order. The rate of chain ramification during oxidation of (I) rises in
proportion with the accumblding amount of keto hydroperoxide only at the
Card 216

28614
8/020/61/140/()02/019/0211
mechanism of-c-ha-in ramifications S130/BIIO
bsginning of the reaction. ~Latsr ont a higher total rate of formation o'
ie7-observed- than- -corresponds -to- -the - deoompos it ion -o,.!-keto.-
hydroperoxide into free radicals. This shows that, besides heto hydro..
peroxide$ other intermediates participate in the chain ramif:ioation
-during oxidationof (1). The assump~icn of a cooperation ot diacet 1
(formed in this reaction and readily decomposable into two xadic&12~ W(LG-
13 oonf irmed by an increasing rate - of chain ramif Loation on 'add Ltion of
diacetyl. - The dependence of the ramiflcation rate on the to-tal concentra,
ti on of ke7tq__hy`d-r`6-p-(s_r`o%-UO-
IPII ka Oal +. ? IPIII
t
Aler-O 0 is- -the rate -of initii~iicn at: -a certain instant -.ol Vqe reaction,-
t- ------- ----
[D) and are, the.- concent rat ions -of- diacetyl- and keto hydroperoxide. On
a mixture o an 4
-2)
From (1) and obtain&
'0
1/02 a ~rDll (+2) ~kw2/okj [P]II/f [,D]2 + (k2/k, IP1,1"k2/ki can easily. be
L-J
a d - 3/6
a

28674
/61/140/002/019/023
S/020
11 a c hr L,, of chiiii ramifications- B130/3110
..calculated sinoe"ths, other data are-experimentally dete=1ned.i-_ he
or-ki- at 1 -10-5 -sW-l for k,- 1-4910'
fouhd7 f 0 sec.l.
~There are 4 figures and 14,references:
11 Soviet and 3 non-Soviet. The
three referender, to Enel'ich-language publications r6ad ea follows-, W. D.
Zdqons~ G, B. Lucas I J, A.m. Chem, Soo. 2267 (19501 J. S. F. Pode , W. A.
Waterep. Jo Chams.Soa-$ 1556P.717i W, A. Watersp J. Chem* 806-P 1946, 1151.
ASSOCIATION: Institut khi_mi_bh.es-koY firiki. Akadsmii- neuk 193P. (Iristitute'
-Aca, Gmy o
of---Chemi oar physiod~of th4 d f Sciences USSR)
PBUITTED. llay~120j 19~1
Sl~i - I..- Kinstid ourvea for the ejonsumption of mothyl-ethyl'k4stone and the
a
cr lation -of --reactidn, products at T m 145 C_ 50 atm, and e.r
ouinu 0 pressure
.*4106ity -s*20-litb:~a/~r$~',,O.I)_Consudption of methylethyl ketanes (11) comi-
-'anam6rphosis-of-curv
e
_16g~vithmid! ourarlation of aoet:.o acid,
W-002i (4Y00# (5) ethyl aceta diacdtYl,~ (7) keto hy6roperoxide
(righ't-hand iicale), -(8) ethanol (right-liand spal a)
--Legsadi hr, (b) molsAb-
Card, 4/6

ZAIXOVI GoIll, MAY14USI Z.K.-, MANUELIS Nome
Mechanism-of chain- branching -in- the -liquid- phase oxidatian of
Piethyl ethyl ketone. Dokl. Ali ESSR 140 no.2:405-4CZ 3 $61.
(MIRA 14: 9)
I.-Institut khimicheskoy Miki All SSSP. 2. Chlen-korrespondent
AN SSSR (for Emanual').
(Ketone) (Oxidation)

KOVALEVAj, Z*Ta.1 ZAJROV# G,K*j SAFONOVAt S,,Kh,,
Therapautia offdai of msuAlrio, ProllstrAry nporto ThAy I-go
MMI 34:434-439 164. 18111)
1, Kafedra psikhiatrii (zav. - zas-luzbennyy dayatelt muki
Prof. V.M. Banshchikov) 1-go Moskovakogo ordena lAnina itedi-
tainskogo inatituta imeni Seohenova.

88359
9/195/60/00-1/004/004/()1r
BbIT/ 05'5
AUTHORS: Blyumberg, Es A.t Zaikov, G. re, Kayzas, Z. K., Emanuel',
TITLE: Oxidation of Ethyl Alcohol in the Liquid- and 1he Gaseous
Phase Under Comparable Conditions
PERIODICAL: Kinetika i kataliz, 1960, Vol--I, No. 4, PP- 510-518
TEXT: The kinetics of ethyl alcohol oxidation in the liquid- and the
gaseous phase were investigated at various temperatures and pressures.
Oxidation of ethyl alcohol in the liquid phase was carried oat at
145-2300c-&nd 52-95 atu. The kinetic curres representing the ethyl
alcohol consumption and the enrichment of the reaction-product during
liquid-phase oxidation at 52 atm and 145, 200, and 2300C appe&r in fig. 1~
The reaction rate increases with temperature. The activation energy of
othyl alcohol oxidation in the liquid phase is 10.2 koal/nole. The.
reaction products of ethyl alcohol oxidation in the liquid phitse at
200 OC and 52 &t0 are tabulated. The main reaction products of oxidation
in the liquid phase are acetic &aid and ethyl acetate. Fig. 2 shows the
CazJ 1/3

88350
Oxidation of Ethyl Alcohol in the Liquid- and S/195/60/001/004/004/015
the Gaseous.Phase Under Comparable Conditions B017/BO55
kinetic curves of ethyl alcohol consumption and enrichment of reaction
products during oxydation at 2300C and 52, 70, and 95 &to. ?ho corres-
ponding curves for oxidation in the liquid phase at 52 eta aud 145 and
20000 over oobalt acetate are shown in Ifig, 3- Both the reaction
kinetics and the composition of the roatition products in gaotame phase
ozidation of ethyl sloohol differ from those in liquid phase oxidation.
In gaseous phase oxidation, CO and acetaldehyde are the main reaction
products. The kinetic curves of ethyl alcohol consumption and the enrich-
ment of the reaction product during gaseous phase oxidation (2000C
20 atm) at ethyl alcohol concentrations (if 2.6 % 10-3 and 0.54 )00 %ole/cia'3"
are represented in Fig. 4. Fig- 5 shows the corresponding curve@ for
temperatures of 200, 230- 250, and 2600C and 20 eta at alcohol concentra.-
tions of 2.6 .10-3 mole/c'a3. The influeace of temperature on the gaseous
phase oxidation of ethyl alcohol at 200 and 28000 and 200 &to :,s illustra-
ted in Fig- 5.~ The CO and M14contents of the reaction productis increase
with temperature. The activation energy for the oxidation of ethyl
alcohol in the gaseous phase is 18 kcal/mole. H, go Semenov is mentioned.
There are 5 figures, 1 table, and 21 references; T Sovieto-8 British,
Card 2/3

86359
Oxidation of Ethyl Aloohol in the LiquL4- and" S/195/60/001/004/004/01")
the Gaseoun 11haoe Under Comparable Conditions S017/B055
3 USt 1 Italian, I Indian, and I Swiss.
ASSOCIATION: Institut khlmicheakoy fizlki AN SSSR (institute Of Chemical
Physics of the AS USSR)
SUBMITTED; June 10, 1960
Card 3/3

BLIUKBM, N.A.;, ZAIKOT. G.Te. K&y2;JS. S.K.; INAMILI , 9.14.
Differences in the Oxidation meclanismB Of OthYl &lcOh0I in
the liquid and gaseous phases. Dokl.AIF SSSR 133 noel;
144-147 J1 160. Wu 13:7)
1. Institut kbimicheekoy fiziki AWemil muk 33SR. 2. "Ohlen-
korrespondent AN SSSR (for Imnuell).
(Zthyl alcohol) (Oxidation)

81726
8/020J60/133/01/40/070
B004/BOO7
S7 oozoo
AUTHORSt Blyumberj[q E., A,, Zaikov, 0. Yevs Mayzusp Z* K*#
Emanuel#$- N* M.0 Corrsi~;ch-dT-ng--Yemb*r of the AS USSR
TITLEs The Differenoes in the Oxidation Mechanism of I!thyl Alooho~l
In the Liquid and in the Gaseous Phase
PERIODICAL: Doklady Akademii nauk 83SR9 19609 Vol, 133, No. 1.
pp.-144 - 147
In the preceding papers (Refs. 1, 2) some of the authors found that
the oxidation of n-butanelin the liquid state is more adva:atageous than in
the gaseous state. In the liquid statef the reaction develops at lowe--
temperature and at a high rate, it is ikore selective and ouch products of
an intensive oxidation as are characteristic of the reaction in the gaseous
phase lack-nearly entirely. N. N. Semenov (Ref. 3) explained this differ-
ence by a change in the ratio of-two competitive reaction3s
ROj,--* R106 + R"OH (1) anii RO; + RH --4 R02H + R' (2). Low pressure and
high temperature are-intended to promote the course of reaction M# high
pressure and low temperature are expected to promote that of reaction (2).
Card 1/3

LK
28
The Differencesin the Oxidation Mechanism of Ethyl SNNY060/1 33/01/40/070
Alcohol in the Liquid and In the Gaseous ?has* B004 B007
B
-For-the-purpose-of ohocklng this a3sumptionp the gutho.re investigated
.the oxidation of ethanol in the liquid phase (200 op 50 atm) and in the
same autoclave also the oxidation in the gaseous phase at reduced pres-
sure (20 ata). The results of both reactions are compared in Fig, I# The
following-charaoteristic features for these two reactions were observed.
1) Liquid phases No induction period, high acetic acid- and elthyl acetate
yield, low yield of CO, small quantities of acetic aldohyde, uhich appears
only-as-an-intermediate product.-2) Gaseous-phases-Long inducition period
(10 h), slow course of reaction, little acetic acid and ethyl. acetate,
much CO, and acetic aldehyde as the main product. Formic acit and peroxide
in both cases form in only small quantities, because they are not stable
under the experimental conditions selected. The authors discutis these
results on the basis of reaction equations. As the concentration of alco-
hol under the experimental-conditions in transition from the Uquid to
the gaseous phase is reduced only to 1/5, this alone cannot lie the cause
of such a difference In the course of the reaction. By calcul.sting the
ratio k2/k. I of the rate constants of the reactions (1) and (2), they find
that k 2/k,, in transition from the liquid. to the gaseous phagie, does not
Card 2/3

the Oxidation Mechanism 81798
The Difforewoo in of 8102QV6011 3!1,10 1 /40/OTCI
Ethyl Alcohol in the Liquid and in-the Gaseous B004/ OOT
Phase
change by the five-fold.bat.a thousand-told. The main factor of the
difference in the course of the reaction is therefore not the greater
density of the liquid phase, but a specific behavior of the liquid
phaseq which may be caused either by intermolecular hydrogen bonds or
by the reaction of Ions laoking in the gaseous phase. There are 1 figurio
and 4 Soviet.references.
A330CIATIONt Inatitut khimioheskoy fiziki Akademii nauk SSSR (Institute
of.Chomical Physics of the AoadeaZ of Sciences, IiMR)___
SUBMITTEDi March 29, 1960
Ca.rd 3/3

5.56oo
77758
SOV/'1'5-15-1-2'-'V~29
AUTHORi Zalkov, G. YU-.
TITLEs Separation of Lower Aliphatic Alcohols ty Paper
Chromatography and Tielr Quantitative Deteminatlon
PERIODICALI Zhurnal anallticheolcoy khImil, 1960, Vol 15, Nr 1,
pp io4-iog (USSR)
ABSTRACTs The ol' methyl, ethyl, propyl, and
butyl alcoholo werc detcmilned. To the mIxture o:-'
alcohol,13 were added 0.5 ml. of pyrIdim-, arid a 3ati.u-~,ted
benzene :.,Olution of ~~,5-dinitroben-zoyl The
mixture was heated at 50-COO for 10-15 nlnuteL.
Absolute methyl alco-..ol waj used ao the otatlonary
phase and heyane, hej~tane, or rionane, az; the mobile
phase. Ascending chromatography waj uoed In the
majority of cajea. Tne solutlon, containIng esters
of 3,5-dinitrobenzole acid, was depooitcd on the Otrip
or acetylated paper (120 X 130 Im) 20 11u1, from the
Card 1/4

Separation of Lower Allpliatic Alcohols by 7775~
Paper Chrcmatography and The~ir Quantitative SOV/7-5-15-1-201/29
Determination
edge of the paper. Tcie~ paper was placed In achroma_
tography chamber after dryinrT. The metil'-d of the
separation is descrillmed by D. F. (Nature, 16(j~
7 Ob
Yanov-;ki wap, u.-,ed a-s a developer.
The ro~-Iulto of U10 tjUallt' I - d C~ I U r-111i L I'! L 10 r1 011 -10 13
V U
are shoaii IiL 111,able 1. T;ie quarititativL? dt, i~,t Ion
:).'L alcohols v1_-1,,-_; baoed on t1he ab.: o 1~ ot icnr, D-,;, 1_1 igh b-,
comoounds fovimed after wr_~re
spra,,,;,,~d Yrtnov,kj. reagerit. Thie, up-,Ical ("(,r,-,:Lty
of alco1iol der' va-111'iv~.s, Itz directly' p,.,opDrtlorial !-,c!
the c~oz~centrar -on. The ex-ror of the me-
I _iod is
Trie rjuant-Itat-iie det(,._rq;Ir-iatIon of alcolhols is pos"11ble
in the presenc7~ of and hydroi,.a,bon oxI.dation
product The 5 1'1jures; 3 and 2`1
Us . j
referencen, T -"Dviet) 7 U-K,, (.1 U.S., 2 Japuiese, I
Aus trA an. Tht- .1) rt~cent U.3.
1). , Hollr.,J, hl',L. W., Al,"t ,Iy G
C
-d 2/1i )52); Rt-1 ,e, 11. G ,, ~1,, J. G.,
a:r 2 1 1 C 1). J . , If

Separation of Lower Aliphatic Alcohols by- 77758
Paper Chromatography and Their QUa-rititat.1ve SOV/15-15-1-20-29
Determination
Table 1. (a-) The value of' R. for 3,5-din1,'1,-r1bePz--,ates
of' alcohols on dIfferent oamfle;) of' acetylated paper;
~b) Type of paper; (c) Movin,,~ phase; (ct) Methyl alcoholl
e) Ethyl alcohol; (fj Propyl alcohol .9
; I ) n-Butyl
alcohol; (h) Hexane; (i) Heptane; (J) blonane.
Q.)
tk) fit /j 4 C
(b o,.-m o,m () 68 (),,77 If 0, 14 0,16 0,41 0,14
0,36 0,50 0:63 1) 0 iii 11 11; 0, 19 11,33 0,44, 0,,,2
0,1~1 (),10 0,71 11 11 (k] 0,26 0,31, 0,49 0,(2
0, 7 2. 11 2
-1:1 o"O v (1,33 11. 51 0, 7 2 0,E4
Card 3/4

Separatit-.'n of 7 7 T! 7)8~
D47 P G'I ~ N.Iji. L LV.1 lp! iY- aril i--T-rj e ~17 f-It _.,i t:L v, 0 i,f71-~ i - j Lj
De tevinination
Analyt . Che,,n., (1951); White, J. W., Drydea,
E. C., Analyll. 20, 85,2 (10;13); Henze, P. E.,
Analyt. Chem., 27, 134c-) (1955); Y. W.,
Phill'iPs, Y. 1'.., AnIlYt. Chem, 2(M, '.`53 lip%).
ASSOC!nTION:. Irl3t.1tute OC Of the, Ac.,tUdcilly of,
fizilk! AN
SUBMITTEDi November 20, 1(-1,58
Card 4/4

BLYUMBMG,, L.A.; ZAIKQ_~e.4--El4AVTJEL' ~ N.M.
-GaB- and Uquid pbase oxidation of n-butane. lleftekhimiia
I no.2:235-21i b-h,--kp 761. NlPd, 15:2)
1, Inntitut khimichenkoy fl2ikl. AN SSSR.
(mane)
(Oxidation)

BLYUIVERG, E.A.; ZUKOVt Q.Ye.; EMANUEL' pN.M.
Oxidation of n-butam In the poeous and liquid phasen, Pv4,
All SWR 139 no.109-101 J1 161. WFA 14:7)
1. Institut khimicheskoy fiziki jW SSSR.,-2. Chlen-korrespdndent-
AN SM (for
(Butane) (Oxidation).

UIKOVP G.Ye*j HAYZUSO Z.K.
Wdation of methyl ethyl ketone in the liquid and gas phases.
KinA kat. 3,no.6t&1+6-854 N-D 162. ~ (KMA 15112)
1. Institut khimichaskoy Miki All SSSR.
(Butanone) Mcidation)

ZAIKOV,, G.Te,; MAYZUS,, Z.X,
Reasons for the difference in t1w mechanism of oxidation of
organic substances In gas and liquid phases. Izv.All &SM.Otd.
khim.nau no.7:U75-11% JI 1.62. (MIRA 15:~)
1. Institut khimicheskoy fiziki AN SSSR.
(Organic compounds) (oxidation)

S/062j62/000/001'/002/01)
BM/Bleo
AUTHORSs Zaikov, G. Ye-9 and Itaysuag Z. K.
TITLEt Reasons for the different mechanism of oxidation of organic
substances in gas or liquid phases
PERIODICALs Akademiya nauk SSSR. Isvestfyo. Otdoleniye khimichookikh
nauk, no. 7s 1962# 1175 - 1104
TEXT: M ethods described in previous papers (Be A. BlIumberg, 0. Ye. Zalkov,
and N. M. Emanuel', Dokl. AN SSSR, 139, 99 (196i)1 Neftekhinlya 1, 235
(1961); E. A. Blyumberg G. Ye. Za*o% Z. K. Vhyzus9 and N. M. Emanuel',
Dokl. AN SSSR 133P 144 6960); Kinetika i katalis 1, -510 (190);
0. Ye. Zsikov and Z. K. Maysus, Kinetika i katalis (1962)1 Be A. Blyumberg,
Z. K. Mayzus, and N. U. Emanuel'# ob. "Okieleniye uglevodorodov z
zhidkoy favell ("Oxidation of hydrocarbons in the liquid phaso")# Izd.
AN SSSR, Mof 1959,.P- 125; 0- Ye- Zaikovo Zh. analit, khiaii 159 104
(1960); 15~, 639 (1960)1 17t 117 S1962))-vare used to stu4y the oxidation
of ethyl alcohol and metbyl-athyrl ketone with different amouats of benzene.
Experimentis with ethyl alcohols 20000p !j0 stool alcohol s benzene ratio
Card 1/3

$1062J621000100-VO021013
,Reasons for the different mechanism**# B117/B180
8 : 1, 2 1 1# 1 1 1_j I-s 2, and 1 t 3. :Sxperiments with methyl-ethyl
ketone: 1450Ct 50 atm., ketone t benzene ratio -, I i It I 1 2,, 1 1 3. In
both cases, an increase in benzene, which teduces the dielectz,J.c constant
of the medium, was found to alter the comp3sition of reaction products.
With ethyl alcohol, the amount of products obtained from the b,'.zolecular
reaction of peroxide radicals was 20% at I 1 3, and 80% inpuro alcohol~.
With methyl-ethyl ketone, (I 1 3) the reaction products had tho same
composition as with oxidation in the gas phase. Differences in the oxide.-
tion mechanisms of polar organic compounds in gas and liquid phases are
due to the rate of the reaction between the peroxide radical and the
oxidizing substance (bimolecular reaction), the dieleatric cowitant of
the medium, and the formation of intermoleoular hydrogen bonde.. The bi--
molecular reaction between RO; and the.test materialt is between two
dipoles and slows down as polarity deoroasles. Good agreement between
experimental and calculated dipole moments confirms the structure assumed.
for the activated complexes in the.case of methyl-ethyl ketonell,but not
for ethyl alcohol. This shows that the re4action rate of ROi and ethyl
alcohol is rot only dependent on the-polarity of the sodium b0; also on
Card 2/3

179 r
3/062/62/000/001/002/QI3
Reasons for the different mechanism... B117/BI80
the'formation of intermolecular-hydrogen bonda. _It -to not the Individual
molecules (RH-and RO;) which-rea-otg but aggregates consisting of five or
more particles linked by hydrogen bonds, Thors, are 5 figures awl'
3 tables.
ksSOCIATION& Institut khimiche.skoy fisiki-Akit6vaii -nauk 66SR--(IfIeltitute
f
o
Chemio 1 Phys ice of the koadomy of Sciences USSVI
SUBMITTEDt January 30# 1962
.Card 3/3

ZAIKOVO G.Te.; MATZUSq Z.K.
...........
Polarity of-the medium as effecting the activation energy of the
chain continuation reaction in the oxidation of 9thjI alcohol and
wthyl ethyl katonr,. Dokl. AN SSSI 150 no,lt-116-119 Ky 10.
KERA 16:6)
IL. Inatitut khimichoskoy fiaiki AN SSSR. Predativlano nkadwdkom
H.N.Seaenovym.
_(Ethyl alcohol) (Butanone) (Oxiiaticn) (Activation energy)

UIKOVJ Q.Ye.
Effect of solvent on the liquid rli!lsa oxidation of etbyl al-
cohol. and methyl ethyl ketone. lleftekhimiia 3 no.31381-389
Hy-Je f 63 044,4j, - (MILI 16t9)
1, Institut khImicheakoy fiziki .0.1 SSSR.
(Sthyl alcoholl (Ketono) (W(lation)

ZAIKOV, 0. Yo.; HAMS" Z#K.61 DWIM10j, N&14*
of chains In tba -I lquid-phase oxidation of methyl
othyl ketone and ethyl alcohol, Noftekht-W,.& 4 no.1991--91,16/+
(,M'IRA 17 t6)
1. Thatitut khimichookoy f isiki. AN SM.

120RUEL lril.32.ay Markovich" ERTRAV, Tovgenly Tlwfeyevich;
XOVS, ZjrnOda r;-wAp,1j--vrw. Frlnlr4all uchastie;
GAGARINA, A.13..~, GOLIDEERG. V.14.; ZAIKC,'Vg G.Ye.; DORIKOV,
YuiD.; OBUKHOVA, 'L~K.; TSEPALOV, P. J-- SHLYAPRITOKV,
V.Ya.2 SKIBIDA, I.F., reud.
1 . I
-[OxidaTdon e-ha In renc t low,4 in the liquid
1,11im)d T.34-!pnyti ojoflilo~l!;i -,,jv'1qvodarodov v
zhldkol faze. 1-11:)Avii, Nau~rk: 1965, 311, p. (141RA 18:9)

01075:160101 -1/005/025/0,26/kAK
~002/'BO56
AUTHOR: Zaikov, G, Ye.
TITLE. The Separation of the Low Aliphatic Ald and Ketones b;r
Means of the Method of Paper Chromato6-raphZ~, and rheir
quantitative Determination 17
PERIODICAL: Zhurnal analiticheskoy khimii, 1960, Vol. 15, No. 5,
pp. 639-642
TEXT: It was the purpcse of the present paper to develop a mathcd for
the qualitative and quantitative analysis of carbonyl compounds in a
mixture of aliphatic aldehydes and ketones (el - C4) formed in ti.e
oxidaticn of n-butane. For this-purpo2e the -paper - --hromat Ograpbic
separation rif the corresponding 2,4-dinitrophnnylhydrazone3- wa13 E,pplied,
The ordinary chromatographic paper of the type
(Laningradskaya bystraya) must, for this plir2ose, first be made
hydrophobic by acetylation with acetic acid anhydride. T~,~ Rf-values are,
to a conaidprable extent, dependent on the manner of this pre-ti-catment;
Card 1/4

Tbe~ Separation of the Low ~Ii I~atic 3/07 60/Oir-/OO%/0r?5/O26/Yj:
P
Aldehydes and Ketones by Means of the Method B002YI3056
of Paper Ghromatography, and Their
Quantitative Determination
however,, the Rf-values are well, reproducible on papers o" one and the samB
lo-t.-Good-separation was o -btai-nod with quantities of 101 g/mole; as a
mobiIe phase, hexane, heptane or nonan6 wa3 used, the effect beirg
approximately the same with all these solvents. Fig. I shows a schematical
chromatographic patte:rn at 200C, where (1) denotes formaldqhyde, (2)
at~etaldebyde, (3) propionaldeny-3o, (4) butyraldehyde,-W acet(Ine, (6)
methyl ethyl ketone, and (1) a mixture of 'these substances.. 2,4-6~.nitrr-
pben-jr1hydrazine always has Hr - 0, Oxidation products such as pej.-oxides,
al-,ohnisi acids, ether, and cater do not affect the chromatographic
determipation in quantities such as are usually formed in the oridat-Ion
of the hydrocarbons. The spots were dyed by means of a 5% scluti)n of KOH
in raethanol, out out, and the dinitropheryl hydrazcnes ar-a ex-tra.-ted and
t,olorim,itrically determinied. The calibration curve practical!y takes the
same course for all sub3tancea muritioned. An tinalysia of an artifinial
mixt-are showa that the error in the determination of aldehy4os and
a.-etones is less than 6%, and amounts to 10% on)y in the saaa of
Card 2/4

'7
-he Low Aliphatic S/075/60/015/00!j/(J25/026/),
The Separation.of t . 11
-Aldehydes and Ketones by Mearis of, the 7-Tathod B002/BO56
Of Paper C~hromatography, and Their
e,Determination 4
(~tmrititatiq
111e-~thylothyllcetono~ The author thanks N. M. Emantiall and Z.- K. Mwrvaafor
diovuosion'a. There are 2 figuroo, 2 ta=os, anJ 18 ioforoncoo: 4 Soviet,
7 13ritich,, 4 US, and 3 Czech.
T 1-0.14 -Inst~itut -khimicheakoy- Tiziki AV -S,SSR,_ Mockva tlmtititute of-
Chemical Physics AS USSR, Moscow)
Sn:,IITT:-;D:, September 22, 1959

Card 4,14

ZAIROTI G Ye -0 - -~-
Chromatographic determination of diace-tyl in the produ-.ts of liquiA
phase oxidation of n-butane. Zhur.anal.kbim. 17 no.l-,117-120
Ja-F 162. ~(FUA 1512)
(Butanedione) (ChromatograplAc analysis)

ZAIKOV, G.Ye.
Separation of 14wer maiphatic aMehydes and katows brr awax of paper
chromtoaa", and their quantitative detersinstion. Zhur. anal
kbim. 15 no.51639--642 S-0 160. WIL 13:10i
1* Institute of Chemical Pbysics, AAademy of Softences, UOS.S.R*9
Koscow.
(AMehydea) (ratones)
(C~romatographiq analysis)

L 360-66 T
---72093!
ACC NRt AP6027349 SWIM; COMS Bu/--- 5j0:[81E2f1695
AUT11011: Zaikov, R*
ORGt now
TITIZi Baryon classification and mansee
SOUP-Cc, -. Bulgarsks *Ymdeadya na naukite,* Doldady., -,Vo -29. nao 12;, .710% 1095-IW3
TOPIC TAGS: baryon. particle pivoics
ABSULACTt The author introduces -a now Urjvn -suporsRat4plat r4CUAA1VU,%Lt1on# . malols
use of the FUto-Sternhaimar rass forada, pautulatea a.maft5 ldfrerolvl.~) 2-alationihip, I
and establishes several empirical for=aas - 7,ae system lis ~testad:by a-Dquu-ing k~s
resiats with knotm mass values 9 Fourteon, nwr baMns 4m -pree,.Utel * IMs, paper was
presented by Academician H. Hristov on 21 Saptomber -1,965. r.Wif;. art. tl2az: 10
formulas and 3 Ubleso fo-rig. art. in. En&2TjJ-M3: j&;46~j
SUBCODEs 20 SM.UTEs -21Sep65 ~OMIRHFs W~
WIF
card

t 383h5-66 EuT (m) /T
ACC -Nito -APW7984 SOU111=_ COD-r'-. __ BU/O0n/66/Oi9_ 5 Tl j '00 1-7- FOO _9~
AUTHOR:
ORG; ln~tuto of Pb
Xgics. BM
TITIBI C3AIMMOStion MA W3806 of
SOURCE: Dulgarska akaderdya na nauldta., Doklady, v. 19, no. 1. 1906, 21-19
TOPIC TAGS: negon, olenentar7 particle, nuclear physics
ADSMINCT: The author 1) introduces'a now schema for -the
labeling of elementary particles; 2) introduCO3 now proscriptions; :5) pn.%poaea
-now malls formulas substituting for the Gall-Man and Olwbo expression;
4).obtoins bettor values.for the equation
-paromotars--oX and Al _than.th0ae__'
from the Flato-Starnhaimor formula; and 5) astablichoo-1 table 01 itiotopio
IPultiplots which exhibit an equality of the 0 and p parities for all
'resonance states while for basic mesons thay have opposite aizns. jhii; :pftP*'o::' was
prosontod by Acadordcian H. Hristov on 21 Soptenbor 1~65--' -5rig. art. 1-i Cn~
rbiw: 36, iV~ff
SUB CODE: 20 / San DATz: 2isop63 OTH 12F: 002
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1,6 V

nu t,,iui~ itierfWcaj cluracteristles
Raj. ob I rd t
anrt Ice.
n t
an Inen
1e
'71 1 (_~
I
57), 10,
Y,
der
The schejrc fcFr 01111i'l-itcl
aposed by Salam and PQ!kit,
P
, 6&5-6901 is extetld"41 t'
;(ILI) 2 (1955), ILI&I
TILO. following eatphic al ftj,lLSsIjc)rmula,-~
for
ions.
ferr,
Held rl is a sixcifir, illteger 0 [ for t)ious. 76 for llud(Ons-
~,O for AG etc.) ar"J I", tai"' tile 0,

ZALTIM, R.
OA sywastrical form of the quantum mechanics of nucleons,"
. IMTIIA. MM FIZICHESKA$ Sofiia, Bulgaria, Vol. 6,1 Jan./Dec. 1956
(published L957).
- - --- - Montbly List of East European Accossions Inder. (VAI)# The-Library-of - -- - - --- -- -
Congress$ Volum 8, No. 8x Argust 1959.
- Unclassified

BUIDARIA/Thooraticel physics - Quentun Theory of Fields B-6
Abe Jour if~of Zhur Fizikaj No 10, 1958, -No 22125
Author s ZaikRyjXAbk&-
Inst Irhy~sics Institute, Bulgarian Acede-V. of Sciences,
Title iOn the Syrnatrical Forn. of Quantum Mechanics for the Nucleon.
Orig Fub tIzv. B01g. A 4d. Viz.-metem. i tokhno I. Sor. fiz., 1957,
16, 3-11
Abstrect ITo doscribo the nucle6n# it is proposed to use e 7-dinentionel
spacul which is a combinetion of the Minkoirsky 4-spi!,,,o and
the inotopic 3-spece. The wave function is consid-gred to
be an 8-componont spinor, of which the first four c,x3pcnents
corroopand to c cberged steto of the nucloonp end thD four
1 ast-c orpononts- to tho-noutral-steto-or - tho- nue loon GIn -a c------
cordance with the Sonerel theory of spinors# the matricos of
eighth order 11 70 Pro derivodl analogous to the
Dirac netrico" The principal equation for tho
h I ?o
nucloonp whic go o In he particular case Into t.ha
Diree equation, is written in theform
Card 1 1/1

BULGARIA/Thcorotical khyoios Quantum. Theory of Fields B-6
Abs Jour i -4of Zhur Fiziks, No 10, 1958, No 22125
j=1
whore(,,.j,(x) exp (ieOk ~), eo and a0 are conatents9 on! x
and denote the first four in the loot three coordinates.
Bi is nado up of pertiel derivativoa with roopoot to tho
corresponding coordinntes end of o!.ghth-ordor tartrizis, which
are 11noar oombinstions of 1, 11 1 () end /-I j ~, PIC P 1 -
It in assuned thet tho cooffiaiontii In those Met c*3 cherw
actorize the intarnetionn with rll types of fiolds, Including
tho fiolds of difforont nesons, and that in the firat sp-
proxi,lAtion they should bu linaar l'unctions of tho ainrao-
ponding vector ond pseudo-vector ptitontials rnd of t.1-m-3 dori-
vetives of the potantiels with respect to the four coordinates.
For the particuler type of the intciraction# an explicit forn
of Eq. (1) is given. At the and of the work the amhor de-
terninos, with tho aid of tho first four metrices Pj,, in
analogy with the Dirac equation, the vector of the mArrant,
tbo pseudo-voctor of the spinp and the onorgy-taimentun
71

A
BUMARU/Nue-16ar Physics Elementary Par.'iit-Liss C -
Abs Jour : Hof Zhur - Fizikap No 5# 1958: No 10142
Author : Zaikov Fashko
infit : ROW-Given
Title : QMant= Mecbanical Characteristics and ElementAry Par+AcJAS
Orig Pub : Dokle Bolgo Ali., 1957.. 10.9 fid-2p 101-103
--Abstract,-: - The - author- considars -the - classiftention of-elamentary paild.-
cles in four di- asio"Al isotopic space.. All the heavy cktrig-
ed mesons are considered as one pseudoscalar part,"..cLe. 11n
neutrkl heavy mesons fom an in&jxin&a4'-# doublet. In tho
classification variant proposed It is possible to dispense-
Vith introducing the lepton charge. However: it becomes neces-
sary to Introduce a hypothetical acalar neutral m-son Vitt.
mass close to the mass of the experimentally observed aeix~,ral
pion* Tile table is given for the classification. of 6lew_~r,4a:,.*y
particlas and the types of their decay.
Card 1/1

BULMM/Nuclear Pivoice - Elenotitary Particles. C
Abe Jour Ref Zhur Fizika, No 10) 1959) 22005
in the version of the theory considered, etroa(; Interac-
tions of the hype are fol'Ind to bo forbid-
den; the wave Vinctions of the K tiesons arA ~hcdr anti-
particles are comectc-d by -the relations K'td* i~ K-,
kO* :~-- -RO. The WO ruesmi cannot decay rapidly into
three pions, -- V.S, Barashenkov
Card 2/2

BULMRIA/1111clear Mysics Elet:iei itriry Particles. C
Abe Jour : Ref Zhur Fitika, No 110 1959, 24446
Author : Zaiko,v R
Inst : Physics Institute, Bulgarian AcadcLW of Scioncei
Title : Isotopic Bi-Spaco Theory. 11.
Orig Nb : D:)kl. BoIG. All, 1958, 11, No 4) 259-262
Abstract : Using the formal-ism previously developed (Referat zhur
rizika, 1959, No 10, 22005), the author writes nut, the
interaction Lngrangl-nns for various types of particles,
charge operators, a,,id baryon nwabers.
Card 1/1
21 -

. Zaikov, Hashko, starahl-muchen outrudnik.
Substance and antisubstance. Rat I flz BuIg 3 no.2:5;3-59 lfr-Ap 162
1. Fizicheaki Institut BAN.

ZAIKO rof. d-rj NIKLEV., S., inzh.
911~
Linear programing. Tekbnika Bulg 11 uo.10096-3r 162.
f