SCIENTIFIC ABSTRACT VESELOVSKIY, P.F. - VESELOVSKIY, V.I.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001859620002-8
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: September 1, 2001
• Sequence Number: 2
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

VESELOVSKIY, F.F., SUCHKOV) YU.D.
General case of tho method for determining dielectric pei ability
by means of resonators. Fiz.tver.tela 4 no.lOt2989-2992 0 162,,
OURA 15-.12)
1. Lenin radskiy politekhnicbeekly Institut Imeni M,I#Xalinina.
Melectric constant) (Electric resonators)

42318
q
S/19 62/004/011/001/014
B119Y33186
AUTHORt, Venelovokiy, P. F.
TITLEs Study of 4ielectric properties of some cellulono estors within
a wide temperature range
PERIODICALs Vysokomolekulyarnyye noyedineniya, Y- 4, no. 11, 1962,
1617 1624
TEXT: The dielectric constants and the dielectric losses of cellulose
diacetate (I), triacetate (II), and acetobutyrate (III) were measured in
the frequency range between 0.6 kc and I Mc 9t temperatures of -150 to
+22500- For all these substances tan 0' showe a maximum at about -200C
and 1 kc, which shifts toward higher temptratures with.'inereasing frequenc.*
At temperatures of j1OOOC and over, tand of I increases exponentiaIfyo
that of Il also increases but shows, at about 2000C, a step which forms
a maximum at higher frequencies. tan 6 of III shows a second maximum at
about 1850C; above 2000C, it rises again. El at I kc rises with tempera-
ture from rV3-75 at N -300C to 4.0 at N +60OCp forms a platform up to
+1500C, and rises again tov4.25 toward +20000. Between -150 and +750C,
Card 1/2

S/19 62/004/011/001/014
Study of dielectric properties of... B119YB186
dipole-radical dielectric losses occur which are assumed to be due to the
orientation of the interacting OCOCH 3 and OCOC 4~9 radicals.. The internal
plasticization involves only a reduction of tand and does not affect the
most probable relaxation time of the dipole-radical losses. Therefore,
as regards dielectric properties, II and III behave like amorphous polar
polymers. The intrinsic vibration frequency of the polar radicals and
their activation energy were determined, these being 10-12 to jo-13 see,
10.6 and 10.4 kcal/mole for I and II; and 10-13 see, 11-3 kcal/mole for
I-II. There are 5 figures. The English-language reference ist R, Seide-
man, S. G. Mason, Canad. J. Chem., 32, 744, 1954.
ASSOCIATIONs Leningradskiy politekhnicheskiy institut im. M. 1. Kalinina
(Leningrad Polytechnic Institute imeni Me I, Kalinin)
SUBMITTED3 October 10, 1960
Card 2/2

SOY/112-58-2-1874
Translation from: Referativayy zhurnal, Elektrotekh-ni", 1958, Nr 2,
pp 12-13 (USSR)
AUTHOR: Veselovskiy, P. F.
TITLE: Lo~w- rFeqaen~cyand ~Hig ~-V-z;eqaency Dielectric Losses in Amorphous
Polymers (.Nizkochastotnyye i vysokochastotnyye dielektricheskiye poteri v
amorfnykh polimerakh)
PERIODICAL:- Izv. Tomakago politekhn. in-ta, 1956, Vol 91, pp 399-412
A13STRACT: Results are.presented of measuring the effect of temperature and fre-
cp;.ency on E, and tgc9- of a number of polymer a of homologous aeries of polyvinyl -
spirit-acetals. A conclusion is made that dielectric losses in amorphous polar
polymers are due to relaxation, phenomena. Dipole elastic losses are found in
all the polymers Investigated, while dipole-radical losses are found in all ex-
cept polyvinyl acetate. As the relathre concentration of styrene in the copoly-
mer with synthetic butadien rubber increases, the relaxation time Ir changes
symbatic,ally with the viariation of the copolymer Tg. The relaxation time also
card 1/2

soy/112-58-2-1874
Low-Frequer-cy axid High-Frequency Dielectric Losses in Amorphous Polymers
changes with complicatLag the side radical. Plastification and cross-linking
tend to displace the t c9 maximum in the opposite sides; they affect Ir and Tg
9
in-the same way. All these factors create prerequisites for controlling the di-
pole elastic losses. Bibliography: 12 items. Ler-ingradakiy politekbn. in-t
(Ler3-1-grad PoIrtecl=rIc b-stitute), Lemingrad.
A. M. A.
Card ZIZ

--------- -
Tjf(c
)/FYF(n)-2 ) GOM
ACC M, APBOI0428 (A) SOURCE CODE: UR/OD20/66/167/002/0339/0341
19
IAUTHOR: Veselovskiy, R. A.; LeJshchenko, S. S.'; X-amont--v-16.
ORG: Phy~~icochemlcaLInstitute im. L. Ya. !~a v (Fiziko-khimicheskiy Institut)
~2__
TITLE: Some aspects of the radiation chemistry of polyMpylone
SOURCE: AN SSSR. Daklady, v. 167, no. 2, 1966, 339-341
TOPIC TAGGS: polypropylene,.gamma irradiation, irradiation effect
---~~MST-RACT,--Structural-c-ha-ngqq-o-.ctw-.,ing in isotactic polypropylene (intrinsic visco-
J-1ifluends- Vf --c0,
bution-of radbcal'and --ionic -reactions to-We
_ess
negligible, presumably because the side methyl groups -cause steric hindrin~ce_ effects-7
which do not permit the polyprclylene chain to come sufficiently close to one another.
Vinylidene-type double bonds wcre found to be r~esponsible for the formation of cross-
linkages in polypropylene. The: cross-linking is thought to result from the interac-
tion between an excited double bond and the polymer clain, and the energy required for
the excitation must be propagated along this chain. The rate of formation of vinyli-
dene groups, determined by IR upectromietry, is much faster below the gelation dose
(6.5 Mrad) than above it; this is explained by a higher rate of consumption of vi
dene groups after the gelation dose. The consumption of active oxygen-containing
C rd 1/2 UDC: 678.742.3:660.85

L 23921-66
-ACC NRt AP6010428
groups may be governed by the following mechanism:
c1l, Clio
if 11 1-1
it it
01 0 off
"Oil
Thus, the decomposition of these groups follows a radial mechanism foilowed by ~he
rupture of the r,-4n polymer chain. Introduction of radial acceptors into the polymer
prevents such rup*,ures and thus shifts the start of gelation toward lower doses. The
paper was presented by Academiciiin V. A. Kargin an 26 June 1965. Orig. art. has: 2
figures, 1 formula.
-SUB CODE: 07/ SUBM DATE: lOun65/ ORIG REF: 003/ OTH REX: 009
r
21216k

"Intermolecular regulation of organic glasses and its manifestation In d1ellectrical
losses and polarization.1f
report submitted for 4th All-Union Coaf on Structure of Glaus, Leningrad,
A-21 mar 64.

V,5
Vxe., -antsyrev
~'LIT12: Pt~enara-'U-ion of Gla~3---: D-Iplula as ~'oa.- the Inie'u- in -3L
"aos
SirLeJ-.W Ck. iv:io L-ra)
d1ja ncpuslmoj L.
F-,~:210DIOAL: r-2iboa?,y i Tolclud-ka- Dl:o2oril-aental 1)57, 11113~ 3, ).10S
U3);-:)R
ABSTMICT In im3s spectro3co,)ic of o1fostance-, --tich a3
free r-,D.~Licals vilaich roact easily with .v-~'Ijals, it is no3e-
~;-ary to ~,prepare ~,-la:;- thcowh vInich thle r;=;
, 0 , U I',' 4D
flovis into t~h,-,, ion A uio'U-hod )f such
n. T'-:' -~,,no. )fa tabe havir.,_- an
~Lrmfn Out to a Jiu-.10ter of
i nternal i-r Of D, -:. ic
r,,i i aw! blic, en(I of tub-- is After
end i-j hOLLtell ILItil th0- softcm3 and. It ir, the-n niercee-
Q -
- _ -, -, - - lt),~ d in
4 Cj,,
t-'iroucrh a -OlFme ;-:,] ,:tz ,s in a my 6c., - .
(Ref.1). Ii 'L-,hick aml j.-1,-.to the
tube. Tiic soal io vc-iLL,i IUL;1j~ LLn(,', vd~%.StanCw Ut.71o-,-)h--riC'
prossuro. T'he ~,an ..!-, 'U-1-1cn covored with Par--ff-in in which a
Car" 1/2-1

Preparation of Cor tha Inlet S~,itoa j--L
Spectrometer.
small hole -L-,: mOo vdth a- hot nebd'Lo
oids o:~ tho CC)V(,!% 0.2C A-r~.GOJ Q1---Ctr0C1F.),4 ~11)1 ~'C,
a
Coil.
potantial. 6
~anlc of :).C IGO
1,111on tho -L?. 'Ill 1.izkI1 i'; -.I. -till"10 1!
aperture 101 It in 6.imneter i-el 1-hp- centro. r1t-
.t, 11 iar,,,-, is rc-
diameter can br, to 3,C; 11 if A. 1, Cdi!!C,
I.,-, Lo )"13ba
peatcd sev,=1 t J)j j
or
fluoric CL(Ad :1-1 bl~ ar)-I)lic17 1; f) f
Diameters D.10 100 to 511U ji :,iLrL 'oo obLoin.- ir, U'.,L~
diaphra-m nay be ftux(I into ~,h~a inlet of vie
spectroia-ter aa; 'shovaa in V.1. Tcd1rozc
ted. T"-,ert) no tabico a~;d 1 Russian
ence.
ASSOCIATION: InotiUute of A,-;~6-13:17 Of
114 1 of UM TjjA (Inatitut khimicheakoy fiziki
A
6994
SUBMITTED: Y)brwiry 59 1957.
AVAILLT.,, rp. T j'- -
0:--cnt-1 2/2 lo Spectrometers 2. Diaphragns-~Glass-AppUcation

VZ,-,rIMS M,- S. F.
Me Comittee on Sts.Liv Prizes (cf the Council (if Mlalsterr* MF.P) In tne fields cf
T
nrJence and inveatlons announces that the folloving scientific worts, popular scien-
t1fic books, sxxi textmsoks ha%nt been submittod for ecapetitIon tor Stalin Prizes for
t,-I,-- years 1952 and (SOVAoM KWtum Moscow, No. af) Yet- Apr 1954
Nam Title of Worm riominated by
Vevelovskiy, S. F. "G.--ass B101-ringli Institute of Chemical
Phy,sics, Acada-,7 of Sciences
USSR
SO'. W-30604, 7 Jtdy 19r,4

USSR/Fitting Out of Laboratorico* Instruments, H.
Their Theory, Construe-Lion and Use.
Abs Orour Referat Mir - Kh-_;'m%a, No 2, 195*7, 4969

Author V~'seloyskiy S.F
-
Title Rethod of Se
aling Toge~her Class of Different Expansion
Coefficient
Orig Pub Zavod. laboratoriya, 1956, 22, No 51 613-614
Abstract Sealing of such 6laGses is effected by means of succes-
sive building tip on one of the tubes of several layers
of intermediate glass varicties, which differ from one
another, in -their xpansion coefficients~ no~ more than
by 8-10~., ana conta".ijiig :Taditally increasing amolints
of the cocon(I kind of glacs that is to be Joined to the
first. A del-ailed de3t.-ript'Jon is given of the techni-
que of sealing toiCctYer tull-cs of qtinrt" and molybdenum
glass, A formula Is gtven for computing the coofficicnt
of linear expansion cf ca raass oll !uiown chemical compo-
sition.
Card 1/1 29 -
---------------- ---------------- ------------------------------------------------------------------------------------------
T-7

F_ LOV YJ
Category : USSR/General Problems - Method and Technique of Investigation A-4
Abs Jour : Ref Zhur - Flzika., No 2., 1957, No 2891
Author : Veselovskiy. S.F.
Inst :-M-stitute of Chemical Physics, Academy of Sciences USSR
Title :Method for Fusing Glass Having Different Coefficients of Expansion.
Orig Pub :Zav. laboratoriya, 1956., 22., No 5., 613-614
Abstract To fuse ftansition grades of glass., two pieces of glass are usually
used having different coefficients of expansion. This article des-
cribes the technology of fueing, whereby the transition grades
are produced from -~finely-ground powdars of the types of glass to be
fused., taken in different proportions. The results obtained by such
fusing are described.
Car(I 1/1

,jj,ff.,y(,v 1,.. ;,.. ; snTIIAT , V.Y a . ; TANT6YRIN, G, D.
K 1y , S . V . ; KUL
PrepRrAtion of 91ABO din!iarr---,ts for eass so.etrometer Iil.etl7.
Prl"-- . ., tell., -a "A's p. 3: I:Y-Je '57.
1. Inatitut khInicha3koy fiziki Akademil nauk SSSR.
(maso Pnectrometry)

1. YESELOVSKIYp S. 1.
2. USM (600)
4. Gearing, Bevel
7. Making small tooth-cutting heads for cutting spiral-toothed bevel gears.
Stan. i instr. 23 no. 9, 1952
9. Monthly List of Russian Accessions, Library of Congress, _ Januag -1953. Unclassified.

. _YMMVSKIYA SIII-9 XDKHUT, A.A., redaktor; SHCHnBAX)DY, P.T., takhnichookly
redak-fo-r.
r)Ifficient procens of manufacturing metal slitting and cutting saws)
Ratsionaltnaia tokhnologiia isgotovleniia proresnykh I otresnykh
diskovykh frox. J(oskva, Gos.ixd-vo obor.promyshl, 1953-25 PANIcrofilml
(Hilling machines)

VEST,LOVSETY, S. I.
Mach-Ine-Shop Practice
Efficient production of end cutters., Stan. i instr., no. 12, 19c1.
Monthly List of Russian Accessions, Library of Congress, March 1052.
Unclassified.

- IMM-m- - - -- ~---- m -1- -
VMELOVSKIY. S,'Ii
"Multi-Frofile Grinding of Thread Milling Cutters
an & Relieving lathe," Stanki I Instriment, 16,
Nos.-4-5s 1945
BR-52059019

-- VESELOVSKIY, S.-- I. --Engine-f3r- - -~- - -- .-- -- - - - - --- ---
HMUtiposition Attachments for Manufacturing Cutters, 11
Stanki I Instrument, 16, Nos. 4-5, 1945
BR-'52059019

VESEL GUM.
Kuybyshev (-1946-)
"Cylindrical Profile G rinding of Glison
Cutting Toole in a MUlti-Position Attach-
ment instead of Reli6veing," Stanki
I Instrument, 179 No. 1, 1946.
ER-52059019

zH
41

-- - -- - - - - - -- WM
- . VRSEWTSjgY- S. -1., Einginear
"Threading Tape with AWYe Dies," Stanki i
Instrument, 16, Nos. 10-11, 1945
DR-52059019

VESELOVSKM- S-.- -- ---- - -- -
"Multiprofile and Shape Grinding of Cutting Tools,"
Stanki I Instrument, 16, No. 9, 1945
ER-52059019

VESELOVSKIT, Serpy lypoyW4 inzh.; SHELKOV, N.I., inak., ved.
red.j RUKAVISHNIKOV,, V.I.,, inzh... red.; SMIRNOV, B.M.,
takhn. red.
(Mam4faoturing low-module gear tail cutters] Isgotevienie
malkomodullnykh khvostovykk dolbiakov. 14oskva, Filial Vaea.
in-ta nauchn. i teklm. informatsii, 1957. 45 p. (Perodovoi
nauckno-tekhnicheakii i proizvodetvannyi opyt. Tema 11.
NO.M-57-15/1) (MIRk 16:3)
(Met&l-eutting tools)

V,ZSELOVSKIYt Sergey Ivanovich; DOBRYNIN, Lp red.
(Diamond -tachining of metal-cuttiAg tools] Obrabotka in-
strumentov almazami, Moskvaj Mosk. rabochii , 1964. 65 P.
(MIPA 3,80)

VESXLOVSKIY, Serg r Ivanovich; S&KMOVI o,y,, kand.tekhn,nauko retsentOnt;
VInz .. reteen%ent; S9MOV# N.I., insh., red.;
KUZMSOVA, A.G., izdat.red.; OHISHKINA, V.I., tekhn.red.
EMnufacturing various types of gear-cutting tools] Proizvodetvo
otdel'nykh vidov zuboresnogo instrumenta. Moskva, Gos.iza-vo
obor.promyshl.. 1959. 158 P. (Ulu 12: 10)
. (G-ear-outting machines)

6-58-2-4/21
AUTHORt Veselovskiz'-.s~.
TITLE3 -M-unicipal Parallactic Traverse (Gorodskaya parallakticheskays.
4 poligonometriya)
PERIODICALt Geodeziya i Kartografiya, 1958, 11r 2, pp. 13 - 10 (USSR)
ABSTRACT: In carrying out surveys in the cities of the Volga district
and on the Crimem Peninsula the author used the method of
traverse with short basis suggested already at the beginning
of the 19th century by V. Ya. Struve. The scheme by Struve
was slightly modified by the author who used a base measuring
subtense bar. The equipment consists of an optic theodolite
Th-40, the base measuring subtense bar, 6 supports, 18 skids,
6 girders and 6 levelling marks. This equipment is packed in
5 boxes of a total weight of 120 - 130 kg. The principle and
the method of surveying is described. It can be seen from
the attached table on surveying in the Volga area and on the
Crimean Peninsula that the here described method meets the
Card 1/2 requirements of technical instruction for surveying in cities

6-.Q-2-4/21
Municipal Parallactic Traverse
as to accuracy. In the case of this method coats are even
smaller as with normal surveying by means of rod supports.
The bar and the accessories were constructed in thc- labora-
tories of Giprokommunstroy under the direction c! the me-
chanic 1. 1. Dudintsov. There are 6 figures, 4 tables, and
.3 references, which are Soviet.
1. Geophysioal surveying-USSR
Card 2/2

-VZSXW7MY I. prof., doktor tekhn.nauk
Self-ignition of coal. Mast.ugi. 9 noo2:24 7 160. (MIRA 13:7)
(Coal minesEnd mining--Safety measures)
(Combustion, Spontaneous)

_~ ~Iyv~-.; sKK~McvA, Ye.N.; 'ItRUSOV, V.N.
VUF_Toy 4
Mechanism of superweak sponaneous lt-m~nes--e-nce of org---r,!!ms.
Bjofizika 8 rio.l;-L25-127 163. lmlt~A 1?28)

ZHURAVLEVp A.I.; VESi--IO'lSKIY,.V-A-' KOSHGW,,,YF-NKOp N.N.
Ploi=iAescencs. T-rady MDIF. Otd. biol. 21s19-50 165.
(MBA 18.- 6)

I
.&TWOLENSHUf V.N.; U.N., NTS1,101101UY, V.A.
of I
Chomiluminescence t*.- ; , bydrogen F-roxidr. an,~ cy5trdrp
reaction prc)duc','-,5, :., -":Iy WIP, Otdl. lAol. 21:112--116 165.
(nvA li~:())

ZIIURAVL~V, M., USELCA'SKlY, V.A.; FLISHCUMIKO, NX. (Hookva)
and of scrie organic CO~-,-Powndfl.
Usp, savr. biol. 60 no.12il'18-197 5-0 165. (M-TRA 18t10)
I. Mentralll-nyy Inatitut kurortolog!i i
fizloterapf.l Pjytisti-rGitva zdrav*akhranenlya SESSR.

L 33674-66 EWT(Q
ACC NRt
AP6004994 SOURCE CODEt UR/0221/65/060/002/0178/0197
AUTHOR: Zhuravlevp_A. I.; Yeoelovskly, V.-A.; KophpheXAnkn,, N~ JK
ORG: Central Scientific Research'Institute of Health ReaRrIg gnd
Physical Therarv o? the Ministry of Heallb 93affaTfsentralInyy naucbno-
.1asledovatellskiy institut kurortologii i fizioterapii Ministerstva
zdravokbraneniya, SSSR)
ITLE: Bioluminescence and'-cbemiluminas!2n2-q-0f some organic compounds
OURCE: Uspekhi sovremennoy biologiiA vs 60, noo 2v 1965P 178-197
OPIC TAGS&. animalp plant., luminescence,, ohemiluminesoenoei-
iochemistry, free radical
ABSTRACT: The present article based on the literature discusses the
physical bases of luminescence, obewiluminescence,of orgenic compound&#
the nature of luciferib-lucifer6ae reactionsp luminescence of higher
plants and animals, and the Importance of luminescence, The
bioluminescent iaecbenism appears to be related to free radical
reactions. Almost all types of biolumineacence and obamilumineacence
require an energy substrate (electron donor), catalyst 11 donor acceptor
(generally oxygen) and a luminescent substance (activator), The
Und-

L 33674-66
ACC Nki AP6004994
position that bioluminescent energy in lost and cannot be utilized by
the bioluminesoent system itself probably also applies to
abamiluminesoenceo Bioantioxidants increase biolumineseence, by
protecting the luminesoent systems from autoxidotiono Spectroscopically
obomilumineseence and bioluminesoonce as broad bands of continuous
light without lines, with maxima In various regions of the visible.
sp66trum* Orig. art. bas, 4 figures*
SUB CODE: -06o 07/ SUBM DATEt rjon*/ ORIG RM o47/ om wwt n7
Card

YAqgpVSKIY -J.., dotsent
I.Y
The committee on the Mack and Wbite cattle has begun its work,
Zhivotnovodetvo 23 no.5276-77 My 1 4. (MIRA 16:2)
1. Sakretarl Soveta po chernopeatroy porode skota pri
Ministeretve sell ekogo khozyaystva RSFSR.
(Dairy cattle breeding)

IZIDINOV, S.U.; BORISOTA, T.Ij VISJWVSXIY, V.I.
Blectrochemical and photoolectrochosical behavior of a
gillcon electrode. Dokl-AN SSSR 133 no.2.,392-395 J1 960s
(MIRA 13s7)
1. lisiko-khimicheskiy iustitut LoTaelarpova. Predstayleno
akademikom A.N.Aru~zWm.
(silicon)

IAZOUM-MMWICR, RJL: AWZU=A, N.A.; VBSBWVSXIY. T.I.
Xectroobemical and photoelectrochemical processes takiZ9
place on germanium of the p- azd a-type in the region of
cathode polarization. DokI.AN SSSR 133 no*3.*620-623
J1 160. (14IRA 13: ?)
1. Ifisiko-khipicheeldy institut Imeni L*Ya. larpovs. Predstavleno
skad. A,,N.Frwukimvm.
. (Gormnium) (076"01")

WITOV.. Yu.A.; ROZENTALlp
ronisation of oxygen o7er punaditse DAL AN WSR US no,lt
152-155 A 163., (IMA l6s2)
is ijziko4qd~ich~eskiy institut in. L.7a. larpova. Predstavlano
skadkdkow A.N. lh=kinyme
(Ox:ygen) (Ionization) (Mactrodes, Palladim)

E S&L o V & K (Y)
Subject i MR/Weronautics
C ar-i 1/1 Pub. 135 - 6/20
AID P - 3300
Author t Veselovokiyp V., Engineer Lt. Col.
Titia Spin of a contemporary fighter aircraft
Periodical Vest. vozd. flota., 11., 27-35# N 1955
Abstract t This is a brief popular explanation of the dynamics of established
wid non-establisbed spin of Idgh speed contemporary aircraft.
SlAns for various initial conditions are discussed and some fig=es
iu.-e given. The behaviour of aircraft with swept back wings is
dosoribed, Diagrams,
Institution t sum
Submitted t No date

ZHURAVLEV, Aleksandr Ivanoviab, kand. blolog. nauk malmyt
Vladlmlr AlekB and rovich; SOROKO, Ya. I.,, red.; TROSHCHIKNKO,
(Biolurdneecencel Zhivoe evechenie. Moskva, Izd-vo IlUaniso"
1963. 1+5 p. (Novoe v zhiznip na-ake, tekhnike. VIII Seriia:
Biologiia i meditaina, no.9) (MI RA 16: 5)
(Biolumineseence)

MELOVSKIY, V.A.; TARUSOV, B.N. II
Effect of )(-rays CoW on the extremely weak luminescence of
the root syAtem of barley seedlings. Vest.Mosk.un.Ser.6: Biol.,
pochv, 20 no.4t65-68 JI-Ag 165. (MIRA 18:12)
____ __ __ E
1. Katedre. biofizikt MoskovsRogo universiteta. Submitted July
24, 1%4-

VESELOVSKII~ V.A,
Device for fastening twaffolds. Sbor. rate. predl.vnedr.v proizv.
no.5:71,-72 160. (IUA 14:8)
1. Magn-Itogorskiy metsllurgicheski:r kombinat.
(Scaffolding)

[-The experience of lending stockbresders of Chelyabinsk Province;
the tree-year plan for the developosnt of stockbreeding In sotioul
Opyt.persdaylkor zhiyotnoyodstys Chelistinskol oblasti; trekhletail
plan raivitila zhivotuoyodstys v delstvil. [Choliabinak) Cheliabin-
skoe obl,gos. Lad-vo, 1951. 151 p. (KLRA 10-.2)
1 , .(Chelyabinsk Province--Stock and stockbreading)

VFZEIDVSUY, Va.
Opyt peredovikov %hivotnovodstva
Cheliabinskoi Oblasti (Experience of forwont work-
ers in livestock raising in Chelyabinsk Province).
1951. 152 P.
SOt Mont~]Z List Of RU3sian Accessions, Vol. 6, No. 1, April 1953

1. V. B. VOSELOWSM
2. USSR (600)
4~ Chelyabin3k Province Swine
7- Useful book ("Practice of leading swine breeders of Chelyabinsk Pro-4ince.11
Reviewed by 11. M. Popov). 3ots. zhiv. 15 no. 2. 1953.
9. Monthl List of Russian Accessions, Library of Congress, April --1953, Uncl.

1. Vh-smovsiay" V. B.
2. -,USSR (600)
4- Agriculture
7- Experience of formost workers in livestock raising in Cholyabinsk
Province,- 1951-
9. Monthl List of Russian Accessions, Library of Congress, April.-1953, Uncl.

vwzibvBxl Y- v 9-10
Me-zhaniam radiational-electrochemioal processes.
Pr:)bl.fiz.kbim. no.1:73-.80 158. (HIM 15:11)
1. Laboratoriya elektrokhimii Ilauchno-issladovatellokogo
fiziko-khimichevkogo inetituta im. Karpova.
(Radiochomistry) (Electrochemistry)

GOCHALIYEV, G.Z.; ZALKIND, TS.I.,--YK$jLOVSKIY.L V.I.
Stationary electrochemical process in the irradiated systerri Pt
(sulfuric acid solution) Au. Dokl. AN SSSR .146 no. 1 131-134. S,
162, (MMA 3-5:9)
1. Fiziko-khimicheskiy institut im. L.Ya. Karpova. Predstavleno
akelemikom A.I. Frumkinym.
(Electrochemistry) (Radiation) (Systems (Chemistry))

AUTHORSi
TITLEs
PERIODICALt
. 38518
B138/B101
Zalkind, Ts. I., Miller, N. B.9 Gochaliyev, G. Z.,
'Veselovskiy, V. 1.
ous electrolyte
Radiation electrochemical processes in aqP.,
solutions
Referativnyy zhurnal. Xhimiya, no. 10, 196k, 62, abstract
1OB416 (Tr. Tashkentsk. konferentsii po mirn. ispollzovan*
iyv
atomn. energii, 1959, v- 1. Tashkentq AN UzSSR, 1961, 347-354)'.--'~
TEM By means of measurements on Pt-, Au- and Hg-electro-
des, a study has been made of the radiation electroMemical processes that
occur in solutions of H 50 and of H so with additions of U(4+), U(6+),
60 2 4' 2 4
(COOH)21 during Co y radiation. Prom the results it is concluded that
both molecular hydrogen and H atoms 19 re ionized. (Their stationary con-
cantration at a dose rate of 6.1-10 ev/cm3 see was assessed as
5 1
2-3-10- 11; this diminished with pH). On the Hg-eleotrode in the prese 'dce
of 02 the H02 radical is reduced. It was found that if the solutiorsof
Card 1/2

S/06 62/000/010/015/05
Radiation elootrochemical processes in B138YBIO1
uranium salts were sub ected to radiolysis, the rate of U(5+) accumulaticn
in the mixture of U(4+~ and U(6+) was twice as high as in the U(4+) solu-
tion. In the, H2so4 solution with (COOH)2 additiones the curve for the
accumulation of H2 in dependence on the (COOH )2 concentration shows a
maximum at N 1 -10 -2 IT. q. 0 formation begins in this same range.
r 2 2
iA*6tract-erls notes Complete translation.]
(lard 9/2

B130101
AUTHORSt Shub, D. 11., Tyurikov, G. S., Veselovskiy, V. I.
TITLE: Heterogeneous sensitization of radiation ohemidal processes
on the interface semiconductor-solution
PERIODICAL: Referativnyy zhurnal. Khimiya, no. 10, ~JA2, 62, abstract
1OB415 (Tr. Tashkentsk. konferentsii po mioi. ispollzovaniyu
atomn. energii, 19591 v- 1. Tashkent, Ali U~SSR, 1961, 37o-37-()
TEXT: The sensitizing activity of oxide semiconductors (zno, CU 0, Fe 07'.
0 2 2 3,. 1'-I`
in the form of agitated suspensions) has been studied in reactions of ra-.*
diation chemical formation or decomposition of H20 2*in an aqueous ooluticn
of NaOff, under optical and y radiation from Go 60 . During the y irradia-
tion of the solution in the presence of a ZnO suspension (261100 ml of so-
lution) the yield of the H 202 formation increases 3 - 5 times. The ZnO
luminescence is found to be quenched in water and the NaOff eolutioh. This
indicates a possibility of transferring the energy of electron excitation
in the seniconductor to the components of the solution. In the presence
Card 1/2

8/08 62/000/010/014/065'
keterogeneous sensitization of ... B138XB101
of 2a203 a considerable increase in the rate of H20 2 decomposition is
cbsi,i?ved under radiation. The rate of H202 decompositign reaches its max-~
imum. at an H202concentration of >20 M. Data for the radiation electro-
chemical effect on a Cu,Cu 20 electrode are also given. [Abstracter's
Compl_(Yte trdhslation-]
Card 2/2

ROZENTALIO K.I.; VESELOVSKIY, V-I. (Moscow); Prinimal uchastiye: PETROV, G.A.
Kinetics of electrochemical oxidation and reduction of Ji2p 02# and
oxyhydrogen gas on a platinum electrode In electrolyte solutions#
Zhur.fiz.khim- 35 no.10:2256-ZZ64 0 161. (MIRA 14:11)
1. Fiziko-khimicheskiy institut imeni L.Ya.Karpova.
(Hydrogen) (Oxy en) -(Oxidation, Electrolytic)
fReduction,"Mectrolytic)

RAKOV, A.k.; VESELOVSKIY -3[.J
Z:t~~ ,-. (Moscow)
Electrochemical reduction of ozone on various metals. Zhur.fiz.-
khim. 35 no.10:2297-2305 0 161. (MIRA 14:11)
1. Fitiko-khimichoskly institut Imeni L.YaAarpova.
(Ozone) (Reduction, Eleotrolytic)

4" i4-
-D f6lo
khimi':" 1~'t6islW 0-2075 -14tl2)
67
il" f SUOU40 oxygon-I

-A
39219
51076162103610071002101,:~
B101/B138
AUTH'ORS: Takovlava, A. A., Borisova, T. I., and Veselovskiy, V. I.
(. moscow)
TIT'AJE. ":"tructuro of the slectiical double layer on oxidized silver
in alkali in the region of the t3~ansition'from the lower to
1;'he higher oxide
PERIODICAL. Zhurnal flizichaskoy khimii, V. 36, no. 7, 1962, 1-426 - 1431
Tj-,,'V*'T: To find oit the cause. of the overvoltage which occurs in the trans-
itiqn rogion, the i-:.Dedance of a silver electrode was measured in I N KOH
the charging inarve nlot-t-~ad, and the photoelectrochemical behavior investi-/
gated. 'Iesults; (1) High resistance and low capacit-inoe were observed in
the transitio~i region. (2) ',','hen the nolarization current is cut off, the
potential abifts toward that of'the system Ag/Ag 2O/OH-. This potential
drop consists in a quick and a slow section to the'eurve. (3) On illumina-
rises linearly with potential and falls rapidly when that of
tion,
the hV.-er oxide is reached. Ithen the illumination stops., the original
Card 1 2

5/076/62/036/00VO02/plO
Structure of the electrical ... B101/B138
'-otential is rostored; here again, a quick and a slow process can be dis-
tlin~_' _-.dished. Conclusions: The electrochemical and photoolectrochemical
bcj',ia/ior of the silver electrode in alkali are connected with the semi-
conductor prope-rties of the system. Due to the discharge of OR ions,
o:cyeen is adsorbod on the lower oxide in the transition region. A barrier
Ia.vor is formed which is polarized in the direction of the cutoff and de-
tarminos the Dotential difference.and the kinetics of the anodic process.
The xt-jor drop in overvoltaZe occurs in the surface lqyer and in the layer
of adsorbea oolarized narticles. The ratio of these jumps depends on the
notuntial and the steadiy-ttato cinditions of the process. There are 7
fi--~res. The most important English-language reference ist 7. P. Durkse,
J. jAectrochem. Soc., 106, 5, 1959.
;WSOMMON: :: to-khinicL
Fizil, heskiy institut im. L. Ya. Karpova
(Physicochemical Institute imeni L. Ya. Karpov)
SUBIM'ITTED: &ugust 18, 19050
Card 2/2

S/020/62/~J�)802/016/016-
B145/B101
AUTHORSt Yakovleva, A. A., Boksovat To lot and Veselov4kij, V. Ii
TITLEt Surfaae states of a germanium electrode during anodi6
dissolution
PZRIODICALs Akademiya nauk SSSRo Doklady, v. 145, no. 2, 1962, 373-376
TEXT: The surface states of germanium of almost intrinsic conductivity
0~ = 42 ohm-cm) and.of n- and p-type germanium of different resistivities
was studied In 9 2so4 and NaOB solutions by measuring the resistivity and
capacity at a polarization of approximately 0-6 v and-&-a frequencies
between 100 ape and 200 kops In the dark and with irradiated surface.
Conclusionst.an increase in anodic polarization reduces the number of
electrons in the electrode surface# with holes being aoousulatede The
free carriers of the conduction and valency bands take part to a different
extent in the anodic dissolution. The reaction proceeds by forming dipole
groups-(Ge(OH)O-) (hole acceptors) on the surface. The liberated electrons
may be transferrod to one of the two bands. Tb* probability of transfer
depends on the position of the oomplex with respect to the energy bands
Card 1/2

S,1020/62/145/002/016/018
Surface states of a germanium##* B145/B101
and also on the surface concentration of the holes. This level is assumed
to be a donor level which lies above the middle of the forbidden ba'nd,
With weak polarizations, the reaction mainly ~rprooeeds through the
conduction band. The downward shift of the Fermi level observed, and
the accumulation of surface holes with inoreasine anode potential
facilitates the 'electron trans-for from the reacting complex and increases
the portion of current abuducted,through the valency band. There are
3 figures. The English-language references ares W. H. Brattaiuq C.
Garretp Bell Syat. Teohn J 34 29 (1955); 0. 0. Girrett, W. H.
4 3 (1;55')-
Brattain, Phys. Rev., 99, i9
ASSOCIATIONs Fiziko-khimicheskiy institut'im. L. Y&. Karpova
. .' (Plhysiooohqmical Institute 1.meni L. Ya..Karpov)
PRESENTEDs April 4, 1962, by A. N. Prumkin, A04demioian
SUBMITTEDs March 30s 1962
Card 2/2

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jot
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new
-
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4 a Ag cwmrd with AO ism studied and (mind to have a
nuis, in the red (not m3rd. for the spectrum 44 equal cWf- "00
MOSUmitatthrestreinevWlilered. ln%O.l X
it loin. with a potentim! correvooding to The equil.
.0,0 4 forms" of ASP the As timro& p- it Pos. emp,
and the outer arg. covw of the doubts eke. Ixyer is due to
go j age
nes"IVAY t 0. Wilk this Plewn as a buls and
by ukkg Ze vp of the pbotowdynnic tffcct late cm-
vMwmian, the nwm prolimble nwhanimn (if this pbwo-
W:rtnu Is rA InUMI The lisht acting rm the
'Jes Its pbotoplyank d1ow". The OD& goo,
trotkomuiretaw chwp and the potential of 11W eke-
too
tfwt drom &COWL to its Polarization Pon" in the
I&nv,=jlmh. 8ft"Idary tkv. pheriormens. may 09041
Iewt 0 libervite4 by the photogalvanic promm. goo,
Thtte are aLverited in the tam cl more pn*. vskin of the
Al rntW of the ttmro& studied than thm III` the rquil. Ze 0
Zk glwtro& after shuffing off the light, A relation
between the measured and tie true values chairvieritins
the phowlialvank proc was found. An
if lkm of The quantum vkld w" nw&. W. a
Wes
00
,:oo
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lot co 0
T A14.1tA w Al. LUSOICA t I, ImA two C4 AllocAme c I- !zoo
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All 11 ON
am MO.,
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A
00 41 4 o. '4S I- Ifit t-
1'. not of the cown. in ih.t Au -#0
00 &?*&fly, it is it function of
cis) 1~spt*. fit N Ill-SA)t at di&rent losill' It"Allis
of A J, slut light intellailors (1). A V Is Prottlotkow tu I 61MI I
pboftWux plCOMM on a ildd 91Ktrodio. V- I. is altefed in the ratio 1:2LI) by chatigi"S like distance be-
GO 1, -00
%1MfQV*if (KaplY lft*t., 36fOK'OW)- -f- PkY1- CAeM..'-* twvm tit,- Au wire anti the "uufce 01i light (A ltiriu-wztt
GO d W.S.H.R.) lo. 2eo-W(IM).-A Au wire, I ("tn. In 1julb) 11W Pralest A V tva* It 9 tit " V. A V is Fero at 0*
of A!I;. didgm. was Immersed Into an Clerfrayle sol". In a sifift-
09 alavordlidlazy. it WON askodically pollariind by "wain of a Vt at A LSHJ%C 1616. 4 CIUM111111ft'.1 3 1' 14 gft4tC'f the 1*0
simdarAutiecimiriaissbniWcspLUAIY.syiiI lislicktritilisill %ttwslkr A; at 37441 A. it is 14111 trrvit. 210) Inneo that ni -00
00 V was detcl. with respect to a Pt ritcimle. previously RAW A - when V .119. The most rapid chance LA -% 1' .00
charged with it. in a third capillary. The All wff"t was rfitb A i4 observed at 513L) A. ji.c., :.4 e.vj. 11 V is al-
Go Wundualed for 0.1-1 we. and the change. A 1'.01 its 110. vt
00 tered frorn 1.72 to 1.59) v. at a neatly ronst. 0 ctioct: ,
jentivill set# tareetwod wit's a string goilvant"neter. (a) (4). the klng,WAVC tbfr$lk*i 16 bildled frUM (M) to 1111110
00 NAPt4, ill N I I'So, at different Thea V Ill =00
A , I.e., by about 0.23 em. Cmierally, whelk V I,% alteml
tionpolarUed Aft sras very small. Mmic a weak const. by me Mis. the thmikuld is shifted by a e.w. At Itter % (;:* 0
00 current WON passed through the wire. a V increased said I t.g.. 37M A.)..% V 1.72 at Y. is sbuut twice that at Uji) v.
rftched a alas. where the potential oil Au liecstme almost 1c) Lxpts. its other scAns.: The rapid rim of lk Von ron-
0 ividet-odent of th.- ount. of electricity pawed. Hdore the
iLnuous ittilarizat ion occurs ai x K Nth at a sukallo no. of I 100o
of pularl"Goo V Willi about 0.6 Volt, the rapid rise of a V evulollittl Palsed and of a " t- (1 .0 v. agatn%t n(onnall
S started at lAv.. 4u;4 the nuia. of a Volesi st 1.7 v. 11 the If clecumle). In X Koff .1 1' 1% Coo stuall (fit nicaturt.
FKAMIJI&M6400 w"-inic"uPlnl, e.g., AftCP 0,0113 cmiumbA uIrni.talk,1114de. milli ).,tiger illun"'14-
had peased through I all. cin. ofth* Au wire, vukd restarted. lions are frthfltA and dicustord. The rhTtrustatit;
a.z.. 30 is". laur. V rapidly come firom 1.3 to 1.7 V. al.
ru ty
though the chugn cb"pd but little. Swo a V changes ,~ Au Is calcd. to be about IW ~ Vt. A
t 4=, of 3 itntarise4 adsorb~f 0 atom I to
Ill, Out main oelt tit the phologalvanic effect: the usajorily
Ut
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WEIMMY, V, 1.
Xlectrodw
Gold
"Photogalvanle Processes on a Gold Electrode," V.
Veselovskiy~ rarPOv Inst PhYs Chem, Moecov, 34 PP
"Acta, PhysicochimIca, MM" Vol M, No 5 1
Istablishes relatIonsi betvaen -gnitude of photogal
vanio effect on a gold electrode and amount of also:
triolty pasood;'and between affect and Intensity of
radiation. Determines spect~&! sensitivity of effeat
establishing its dependence an electrode potential.
Discusses probable machanlen of photagalvazld pr6de4a
on gold electrode. Received, 26 Oct 1945.

004
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00 t
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0,9.3
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S
R
rRit.) MOM,), 2-
(in Ritdan).- 13"
Y~n=de kally Polarized In
0.1 N KaOH and thertfore coated with Zoo is sensitive to
-ultraviolet. The curve o( leaAftivity against tin wave
length X Is Omit Coincident with that of light abwepilon
bY ZD0 ASSIO" k. It The ZG/ZnO flerfrole h polarized
to + 1.5 V. AglAgj() In 0.1 N X&OH and Wurni.
na", the C to -0.6 v. The PAA
Ag=wk
current between ilrometi Zn/ZuO and Is
=ional to the light IntensIty. The quanturn yiel,l
O.S. This shm" that the wbok ZnO layer, not
_Just Ith mince, is active. Front the varialtat" of
and current simseth the electrostatic capactly a( the w.
tive syment Is about 301 pt./sq. cm. The abfte obser.
vationt ate used to explain the photomernitizing effect of
ZOO. J. J. BiltmnAn
affALLOKICAL Lrfg#ATWE CLAIWICAIM
slow fly.flivo
Ida*" so I " -~.
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0000000410060000090000410
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ad
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PA 56/49T16
Q;M/ChWGti7 - liectrO&Wstry Doc 48
Chemistry Photochemical Reactions
~Sensitlzaticn 14echanism of the Photoel aotrochomical
llrocesb oft'a Zn-W-Blectrods," V. 10 Veaelovekiyp
Fn,78icochem Inst imeni L. Ya Yarpoy, Nbecov, 16 pp
"Zhur Fiz Xhim" Vol =J, No 12
Sti.dies unusually high photogalvenic affect cn an anode
paeolvized. Zn-eltictrode, and. shove relation between
mechanism of photogalvanic phenomena and macbanism of
hatqrogeiaeol~s', (pIgmentaryY se-neitizatiop In aolutlciC
Also demoneiratec effectiveness of photoolootroebomiddl
nothod. for obser-4ing anode processes, particularly
in cases of passivizing metals. Submitted 8 Apr 48.
IMP 56/49T16

/Chemisi,ry - Xlectroohenistr7 Nov 48
I Chemistry - Photochemical Reactions
"Jbcbanls= of the Photoelectxocbemical Processes
an an Ag. Ag2O-Xlactrode," V. 1. Veselovskiy,
ftelcochem Inet ineni L. Ya. Marpov, Moscow, 10 py
*Zhur Iriz Ebim~' Vol XII J. No 3.1
Determines photogalvanic nature of a reactive
group of atcmB an an anode polarized Ag-electrode,
azA establishes relationship between 13hotogalvanic
current and electrode potential. Determines spectral
sevaltivity and. red border of photoelectrocbezdcal
pmoess on Ag-electrode, and suggests an explanati=
of the mechanism. Shows the specific character of
USWChemistry - Electrochemistry (Contd) Nov 48
pbDtoelectrochemical deposition of oxygen and
Anodal oxidation an the Ag. Ag2O electrode, aid
the relation between the process and heterogeneous
smaitization in a solutim. Submitted 8 Apr 48.

30727. VESELVISICEY, V. 1.
Fotoelaktro'khimicheskiye protsessy na theleze v prioutstvii parokisi
vodoroda. Zhurnal fiz. khImii, 190, vyp- 9, c. 1095-105. -- Bibliogr: 7 nazv.

C A
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thkk) Iry anotlk PolAtUaliull or fly 11"Iltif III Of brn%mr,
On 8 N'4010 with *&Vf Withi X.
this 4rUvtto& AM a A41AW) rtmtrwk, k* v" r unall ;a.
kW 16% the 11011ANi"I" V%41AKV t'i% k" 11114111 (13 V- AWI
r.agilv laor"" with V at "Itt Analk 44,
PC. In light. the Ctme"t 1, is OUVI-val4c *I V - --it's V "
iocir-swalaith VU1WsrIV maid it rvolUMM otalts 4*1 013
V, 1 411.1 kiWtfdACI "We tAwly with V41 V imme 11M11113
v. At a MUC h. V is ralw*1 foisof, e.g.. 0.3 to it 6 v.
withbi I stic. (awillogrAph data*.) but rapkily rouriso to
the oricitW valus ou. tuming of the light; (be capacity
C of *be tkctnxk Wems to be about IW during Uluniliu-
tiua itud about 10 p F./sq. cm. duriac darkening. In X
.NA()"[ + I to 1.8% 11M, ViLkliml Ff is light-orusitivv-
~6* witbout poUdution as Jung as A is ten than 4W inp.
V is -0.2 to -02,r. without. aM. e.g., -0.4 to -0.0 v.
in 10t. The light value of V is achieved in. e.g., 0.5
-av.. mW C Is alixiat 60,plf./sq. cm. With pola6-tion.
to - to Wfftllft With I'IUWA$ly bCtWC9U -0.6 And +0,;'
v. This li-ri )r is accounted for by assAming that light
de"cupd. a higher O"k (or act oliorptim compd. of Fe
oxwe with 0) Go the ckctto&. that the rate 0( this &-
CMISO. nproportional to the ftmfod thettrFl!"k4edtht
clevtooleby4hitaskle.andthAt. Visitlinessfuuminnol#
fh" theory pordirls that the Mile"'ity W FWbAsk)" J muf
I he ~Vucn- 4. of 11" Affect V Acrue.ling to V - t Vonc +
JJJ. A is Coast,. atki qiul. C%pf4. a" ist acir""C"t With j
It. Siam the qwxatum YkU of 1. - ji may be " bighas
0411. the subotalict iibnoebinj the radiation preminably is
Pcith rather thm the higher oakk pirsent in an kicum.
Olt irsintiol, law. J. J. LIArrinan

,CAP
ocattt; aad mochAnim at Liberia-
on "I ,,;-at -.,ktr.7- V. 1. Ginsburg
and V. I. NsedowskI64KArPoir fmal- P1175. Cbm.. Mos-
- JN#. X". 24, MOI,43(11166): d. C.A. 44,
Zv. fula'. t1d V of a Pt eleetrotle In N If9m
after "Verml = good cathodic polimrisatiomi . O.W 1.
rtfmed to N Its electrode. It this Ill electrode we- -noll-
cally polariad to Vs v., ft I m pbotomemaltive. and the!
light gradually low-ed V back to 0.9 v. The rate of de-
crrAn of V Ut the greater VI (1.W1 M V.) WAA,
the greater atenskyl. The pbotodecftacbm.
CA. i was 4-E. to I OW the "t of V was a linear
function 41 %1, TM W longer than 4M top was in.
sedw, a" I mcdvky "MOMI with fietim icy lip to
2sm nip (an shortest wave und); at 284 tno the
pbotodgctmw wed 0.3% for the=
rghm'. Of V=,7. d inorneed with V, abnast Umnly as
lonS*sVw&msmAIL lUelectmdecsWitYle"APPOI.
3(t) microtands/sq. cra. for both dark and light processes-
When a Pt electrode was amik-aily pokrimed to V,
tnure then 1.5 v. viel its surface was then mduced cathodi-
Cully. the V was for & tium cixnt. at 1.5 v. and about
vilkil:.; cuutornbe/sq. Cm. -to n4pi6d to lower Ow V.
that the Pt surface, was ievvttJ with a numo
layer a higher adde. Irradiation wW cathodic poIsriZ4
tion caused decompa. of this oalde mam r2*HY than
either of them m3me. The Increase of 0 overvvitao on
Pt WAI: I-reLsing CA. awned a kink at 1.4 v. The
rnachmalm of Lbe pholmeloceroclIMM. effect indufles
liberation of an electron in Pt oakk tT light. migration of
this tiecuon into thit wetaL amid thme 'electroo de-
ficico-y" toward the solo., and discherge of Deq. 0 (am-
ing a part of the higber mWe. ). I. Hikerma"

(4MIMM.- V-T-i tln-S.,-10 ~rl
Electrodes
!Iechanism of action of optical mdiation on an a-nodically rxidized learl electrode
Zhur. fiz. kh:Lr.. 26, TTo. 1, 195?.
Yonthly List of Ikissian Accessions r of Congress, Septenber l?52, MICUS-STFIM
_L LJbmr

VIM/Mumistry - Photosensitizing Catalysts Apr:`:59.
"The Photoelectrochemdeal. Prt)eess in the Micro-
heterogenous Sensitizing System ZnO Suspension/
Solution," V. 1. Veselovskiy, D. M. Shub, Phys
Chem last 'men' L. Ta. Karpov, Xoscov
"22,ur Piz Khim" Vol XXV , No 4, PP 509-519
0
The ZnO photosensitizing syptem, which is of
Uportani-e for clarifying the action of biol
Photosensitizers (chlorophyll), and for studying
the stability of pigment-contg rubber, paints,,
md lacquers Uroard light was investigated by the
method of anodic polarography under use of a
rotating Pt microelectrode. The mechanism of the
process studied,, -ahleb involves formation of
ff~~Ot, may be interpreted
,, in the presence of 0
a3 In electrochem result 9i the extinctIon of UO
fluorescence by oxygen. The Wesence of an org
reducing agent (glycerin) sbarply increased the
photoelectrochem, process on 7mO. At the saw time,
the effectiveness of anodic cxidation of plycerin
&t the Pt electrode is increased ir-an the 2-a' tter
is irradiated with a wave length active for a
Pt.PtO electrode.

wzlence And irvtntinr
.w tntt
tific boDke, -n4 Vpk-tbot*s have t.-een aibmitted fc)r ~vjqra%ition 4,0.. fizi:-
t6e yemrs .119~12- And 1,9~3. (SovetrsLakLEt!L~~n~s Kosv:m~ i*-,. Feb 1~54)
None Mle of uori~
Veselovskiy, V. I. "Photoelectrocherical Finistry of Uhm. CheTAcri
Inve3tigations" Industry
jqjj 1;.~54

VF_sct_ov!~~K%Y, V. I -
The wechar&m
ib" of
Uyl~
Prows'
is.
(eg., Oh
.-A Pt wbv
ted In a main
e
OW r
rn
CM U &,ed
g
~
.
.,
.p.
I
the e Me In toMphy If It was polarlwd 4 times ht 3
[W
the tW o - L&OA Y
irlative to the N H
.
.
-w
ve
e
tent(
l P of 1"I
n Onode
h

Chemical Abst. .
a
a
c
a
po
~wu 1.2 v. In M. If C104 N HM4 Iand N 11140s, and the
IbWd" current I was Independent of the rotatiz-A o( the

Vol.-:48 No. 3 i.e. vra# detd. by the rate col charKl% the ekL-;
ig$Oo + d1l. NalM, R was 0.7 S v., Le.
Feb. 101 1954 the omvottagt was appm. 0.8 Y.; whim the conen, of
Electrochemistry M- Incretied 10 times, t atto Inentasmi 104*14 and St
b
i
A
was more anodle
decreased
y 0 15 v.
t v > I I curreqt
when f? hweamd, an~ at v - 1.5 ~, It wm 0.1 that atl
_
1.06 v. An anak ftdc
# &
ee Of 0 on i was obs""d
r d for AV 1114(N + 0.0003M
O.M
I S and
for M II.SO# + 0 JW
KNOI (with 8 - 1.23 v.). No finAl tiplanation was x*1-
N 11
40
i
k
h
d
iLb
for t
0.01M X 1
ecrease at
at Wher v. In
e
. +
N(h tM4 In JY HCIO& + WIM HA (E - 1.19
11.). a Sad wave occurfed at go - 1.5 v.; It may be due W
decompn. of a Pt Ide. When v rA Pt was Increased
p
r1
dl

M
y (e.g.
02 Instead of O.W1 vjsec.), I was
W
tee ".C., 4 X 10-4 Instead of 2 X 10 amp. Id M.
because I .- ft + C(doldl), where A was them
of canvat due to depolzarims. C the electrode ca,-
losefty. and kime. The1h%YHtW#+O.W5MFeWww
Inclem-d-Cof dfld$ bea"m Poll- ~ Fe", was " elec-
,
--
4ixik- The dectrochem
axi&tion of 80
.
.
,
NOs-, sud MA was detd. by reactions between tftc* vib-
t
d W 0
d
b
d b
P
lk
s
anew an
e
a
xw
er
y
t, J. ItA
J,

lie-

F_ L_ ov Y" v.

6
151. istatbe of the tha elet troelteatical If
UT-J. Borisov
of
of
of~
(L m7litm. Inst.
is. M.
0
F;OntIlEMM14 ~IkKl" "Y
p abstir.-MectrodiCM. 01116110111 '1 as to. In
ch oxidation by surface oxides, AM the furo.-tion of the
elec. evrent was to re-forus these Oxides after licir redue-
tion. The diflerential cip4eky C and the resi4.uu-c A j4_
Lhesutfaceolawive were detd. bjcompatison-Akhac;Iv~0$wV_.
itance and a reststance III otirks. (a) Mtn the pitittatial'.'-

--

emical Abst.
V01. 48 No. 3

Feb. 10o 1954
Electrochemistry 1P (against 1Y H ekctro&) of Ag in N NaOll wns Crulu
varitojr -11, 10-1 v uAdCantiRwrictIct
Sc. 0t a 1: el :. 6 0 - tirlax-. it
11. (formation of A surface oxide), 1.2 v. 0 prinatliviv -
anti 1.5 v, (formati(in 4 higher Ag uxi&4; in
this hilheit nt~ix., Was 455 tniclufar4di/sti. C111.): (ho,
shallow min. at OA v. co"tsponded to zero charge of midizW
Ag wrr:wc. ant! the deep min- (C - 20 inicrofarivis/Mi. ctnj:
at I Zv. was due to lower oxides which vvere pootty conduct-
hig, as R otherwise small. readied 101 ohm/sq. cia. nt 1.3 v.;

v-1
Tbe nim. of C at 1.3 v. was vWbic also at 101 tnyclrshiee.,~
while Al the other mix. and min. disappeared. The R!
deermned when frequency Increased; e.g., it was 2.5. 10.000.
and 99 at 5 cydes, and I a, 9.1, and 1.8 at 104 cycles for v w
0.4 1.4, and 1.65 v., resp. M Pt in N 11tS04 hatt a min. al,
C 125 microtands1sq. cm .) and a max. of R (2 ohm/sq.
on.) at 0.0 v., i.e. at the potential of Pt oxidlited by uLir,.
Amax.(A Candshaillowmin.of Roccurrtd At Uo v. (forma-

-
tion of' a hish-canducting higher oxide). 7bis tnax _M
of C
was vkible between 2 and 20,000 cycks/sec. alsobt N IlCtOto:
but it disappeared after a strong anodic polari=ttiou of IN.-
Ilic p3tential of zuo charge of Pt was O.W v: in OOMN.
:7- Ab
max 41 In &r ds/ cm, 27 t ~M%.) 4t.0
am thaii,the if. tillial but At
In
the o U oaddlud Pt, this Owwed that _-WaSoxiiii, Iby
surfati: oxides. Chatiamin.atI.2y. Oxidatio 11
started at 1.05 v., Le. 0.1 v. room anodic that -
to tial. ~ (hi the contrary, C in N IItSO4 + t FMI
ta max. at 0.77 v., Le. at the equil. potential eca""
surfav: oxides did not participate in the
Te*1". ONKutiono(EtolltoAcllocctu=to.'7~o
and to Idatiogi of AdI to ArOll, sit 13-1.4 T. Jj

VESELOVSK Il V.I.
(Radiation aboulatry processes In inorganic eyote", Zlectrwbe=ical
offset of radiation. Sensitizatim of radiation chemistry reactior-al
Radiatsionno-khWobeekie protsessy v noorganicheskikh sisterakh.
Elektrokhimicheskoe d.eistvie izluchenii* Sensibilizatsiis, rediatsion-
no-khbicheskikh reaktsiL Moskvap 1955* V pe (MIRA 14:6)
1 . (Radioohemistry)

VIZELOVSM., V. 1.
"Radiation-Chemical Processes in Inorganic Systems,," a paper presented at the
Atoms for Peace Conference, Geneva,, Switzerland, 1955

on of Vift the 0&tins6n e,'cc,
the
tr
loliala. In
the rwice 0.05"X(N) v. 14-Ution c4 the electruc!c i---
creised curr,~nt by 6-9 times. Tli-I adda, cf
.id $01,
0.003N HA!A to the miludc tv~ .1. incrranl tue Cur-
ra:t by a Uctvr Of 5 for 1xith statlenary :krid roti.ting cla-
trl~.Ics. C. It.

'7
Category : USSR/Optics - Physical Optics K-5
Abs Jour : Ref Zbur - Fizika, No 2, 1957,N) 496o
Author : Veselovskiy. V. ' Shub, D.M.
lust : Mysi7cchemistry lastitute, USSR
Title : Mpchaniem of the Formatior. of Hydrogen Peroxide that is Photo -Senqitized
by Zinc Oxide and the Fluorescvmt Pry.~perties of Zinc Oxide
Orig Pub : Frobl. kinetiki I kataliza, 1955., 8y 53-52
Abstract : The euthcrs sum up the results of an investigation on the mechanism of
the heterogeaeous reactioas of the desorption of 0 from ZnO, photo-
seLsitired by zinc oxide a,_t~A of the formation of 40, in an aqueous so-
luticm in the presence of 02, and the connection b6tween the sensitizing
ability of Z0 and its sadconduct-or and fluorescent properties. The
high quaratum, effectiveness (u,1D to 50% in the case of incident light) of
desox-
ption Is caused by the sensitization mechanism of the process: the
radiation absorbed by tht emt1re volume of ZaO excites electrons (a1w.
h_-leO vhIch migrate to the surface, causirg a chemical reaction (desorp-
tion of 02)' Z-- the H,,,O -formatira reaction, the oxygen aisorbed from
the ZnO cdl7tures the ele9trms that ore excited by radiatii= 02+- e
Card 1/2

Category USSR/Optics - Physical Optics K-5
Abs Jour Ref Zhur - Fizika, No 2, 195T, No 496o
%0 --,%0H- +- (1/2) IL
~20_ t (1/2)02, and the OH- long of the alkali
give up their electrogs to ZnO, Wich reecanbine with the holes: OR-T-
e +_.~ (1/2)H~,O~,. A eingle-valued connection is observed betveen the
sensitizing a-bIlity of ZaO and its fluorescent properties-. 1) frequently
one observes for various specimens df Zr_O a symbasic connection betveen
the sensitizing ability and the intensity of fluorescence 1; 2) the
curves sh-mring the dependence of the sensitizing ability on I and on the
sintering temperature of ZnO have a similar appearance; 3) the specimens
of ZnO having the marrinnun sensitizing ability display the.mrJoun ex-
tinction of fluorescence by oxygen. Calculation shov that in the H20
forms,tien reaction there participate both the electrons responsible igr
the fluorescence, as vell as the electrons participating in the radia-
tionless transitions.
Card 2/2

N
n, l~-
I
I I

-50

to

flint In
'hc

.aF foun't 1~ !t:r tl!'fa-!fT
rx, ~ r , -Aw-
~
w:lslf
: , ".
"trMD"Ir
4110-vm tfftwa mmm Azsm Am"',

~7
H
1-48ELOYS V. I of
I Y
"The Yechardsm of the Radiaticn-Electrocherdcal Proc*rses.,
report presented at Scientific Ccnference at the Inst. for ?hysical Chemistry
imeni L. Ya. Karpov, Acad. Scl. USSR, Nov 1957,

Bm' N.A. . ,ITof.0 otwetetTenw red.; MOVIDW, S.S. ;,TXSZWSKIT, V.I.,
prof,'.; DOLIN, P.I.,'doktor kh1m. muk; Mum.
nam f kands kh1u. nauk; 2WCOFOY9 Dol, red. izd-va;
BUGKMSX4Tj*T*, red. lzd-va; KOSUICHWA, N*I* tekhn. red.
[Trazimations of the 71rst A33L.-Union Conference 'an PWAlation Chemistry],
Vaesedume edyeshchanis po radiatsionmi Wall, let, Ko9oowq X9570
Ti-u4-,*', Moskva, Ixd-vo Akad, naWc SSR, 19580' 330 pe (KIU 1:47)
1. Chlen korrespondent AkuUmil mank SSSR (for Nedwedev).
(Radiochemistry-Congresses)

AUTHORS: Rozentall, K. I., Veselovskiy, V. I. SOV/76-32-6-23/46

TITLE: The! Process of the Electrochemical Oxidation of Tetravalent
Ure,nium on the Pt-Electrode (Protsess alektrokhimicheakogo
okisleiiya soloypchetyrekh -valentnogo urana na Pt-Elektrode)

-kEk0DICAL.--- -8-- Vol
I i~ is Ahimiij 195 9-
-zhifilial: it lid --32i-Nr 69
1341 - 1347,(USSR)
ABSTRACT: This work was carried out at the Laboratory of Electrochemistry
of the Physical-Chemical Institute imeni L.Ya.Karpov between
191;8 and 195o; the technical report is to be found at the
library of this institute. At present few data are found in
papers dealing with the problem mentioned in the title; among
thom, are the papers by Bette (Ref 1) and Real (Ref 2). The pre-
sent investigation was conducted by means of a rotating Pt-micro-
eloctrode using an already earlier described method of anode
polarography. From the obtained results of the experiments of
tho anodic oxidation of
UO'~2-ions in HC10 -solutionsas shown on the current versus vol-
4
Card 1/3 tagre diagrams a ways may be seen at E 1/2 w 1-05 V, as well as

The Process of the Electrochemical Oxidetion of .50Y176-32-6-23146
Tetravalent Uranium on the Pt-Blectrode
a current Id = 4-3AA directly proportional to the concentration
of the UO+2_jons within the interval of from 1-10- 2 to 2-10-4 M"
It was found that the value of I d depends on the surface of the
Pt.-electrode, as well as that the Yalu* of I decreases with the
d
retardation of the decrease of the I - E curvet so that, for
inotance, in the case of an increase of the velocity of the
potential application to the 8-fold an increase of the limit
current to the 2-5-fold takes placeoln order to make use of
this knowledge in the increase of the sensitivity for analytical
purposes some conditions must however be taken into accountg
Baved on the evidence obtained and on some rules it is assumed
that an interaction of the UO+2-ions with oxygen which is alectro-
chemically adsorbed at the platinum takes place and that It do.-
termines the velocity of the reaction mechanism. The electroche-
mical redox processes which take place only due to the exchange
of ion charges dop however, not need any activation energy and
take a reversible course. The investigations of the anodic oxi-
Card 2/3 dation of UO+2-ions in the presence of H 0 and Cr,1*3-ions,
2 21 HN03

The Process of the Electrochemical Oxidation of 76-32-6-23/46
Tetravaleni Uranium on the Pt-Electrodo
its well as HHO 3- solutions with Tjj+4-ions ahowed that a chance
of the I-E curve occursp wherer e.g., a higher concentration
of tho Cr+3-ions can caust the adsorption of the Gr+3-ions at
the Pt-ourface. There are 7 figures and 9 referenceBt 6 of which
are Soviet.
ASSOCIATION: -Fiziko-1-himicheakiy institut im.L.Ya.Karpova,,L'oskv,- (Institute
of ftsics and Chemistry imeni L.Ya* YArPOVp MOBdO'v)
SUBUITTED: February 16, 1957
1. Uranium--Oxidation 2. Uranium--Electrochemistry
3. Platinum electrodes--Electrochemistry
Card 3/3

YAKOVLEVA, A.A.1 BORISOVA, T.I.; VESELOVSKITO V.I.
State of the surface and mechanism of the oelf-disoolution of
germarAulp 4n hydrogen peroxide solutions. Zhur. fiz. khim,
36 no4U~2341-254i, N162, (MIRA 17:5)
1. Fi2;iko-khimicheskiy institut imeni Karpcria.

AUTHORS: Tyurikov, G. S., Rozentall, K. I., SOV/76-32-7-8/45
Veselovski7
j Y. , 1.
... ... ....
TITLE: The Mechanism of the Electrochemical Reactions on a Mercury
Cathode in Uranium Salt Solutions (Yokhanizm elektrokhimiches-
kikh reaktsiylv rastvorakh soley urana na rtutnom. katode)
PERIODICAL: 2;hurnal fizicheskoy khimii, 1958, Vol, 32, Nr 7,
I)P. 1490 - 1498 (USSR)
ABSTRACT: The electrochemistry of uranium has been investigated by a
great number of scientists, there are, however, a number of
contradictions in publications# In a previous paper one of the
authors of this paper carried out polarographic investigations
on a dropping mercury electrode, as well as on a steady mer-
cury electrode in the case of a weak polarization by alternating
ourrent;' these investigations dealt with the electrochemical
reactions
2+ 2+ +
110 + ee----'*UO+ and UO + 0 UO . The polarograms of the
2 2
cathodic reduction of uranyl ions were automatically recorded
Card 1/4 on a polarograph according to Geyrovskiy, the work having

The Mechanism of the Electrochemical Reactions on a SOV/76-32-7-8/45
Mercury Cathode in Uranium $&1t Solutions
0 0
been carried out in a hydrogen atmopshere at 25 + 0'1 C. In
the investigations concerning the influence of the concentration
of H+ ions and of the nature of the anion of the solution
on the prooesn of the cathodic reduction the author used con-
stant uranyl ion concentrations in solutions of sulfuric acid,
hydrochloric acid and HC10 4* The current versus voltage curves
obtained showed two and three polarographic waves respectively#
corresponding to the acidity of the solutions; the first wave
is explained by the reversible reaction
UO 2+ +e ___""UO +1 while in the presence of three waves the
2 2 + + 2+
second represents the irreversible reaction U 2+e+2H---3pUO +
+H 0, and the third wave characterizea the reversible reduction
2+ +
of uranium from the tetra- to the trivalent state UO +e;F!uo
The I - E curves of the highly acid KC1 and H2 so4 solutions
do not show a+second wave and a dispropoitioning reaction is
assumed: 2 UO + H+4==t UO~++ UO(OH)+. The function of the
2 2
Card 2/4 value for i d of the first wave vs. the nature of the acid

The Mechanism o:! the Electrochemical Reactions on a sov/76-32-7-8/45
Mercury Cathode in Uranium Salt Solutions
artion is expreased.by the series
id H2SO 4~i d HC1'>'d HC104and it was observed that the effect
of the anions extend to the various stages of the cathodic
roductin For detarmining the velooity of dinproportioninR
of the UO 2- ions an apparatus was used, with the neaouring
mothod having an advantage as compared 'to that by Heal (Ref 6),
viz.,-that the measurements were carried out directly. The
technique of current measuring in the determinations carried
out in the exch ge reactionsrUO2+ 2+ ---;p
+e;p-UO+ and VO +e.&- UO+P
2 2
lav well as the apparatus has been described in the paper by
K.I.Rozentall and B.V.Ershler (Ref 11) '6 From the results of
the investigation mentioned may be'seen that the electrochemical
roduction of U02+ in UO+ determines the velocity of the ex-
2
change of the first reaction. It was found that the exchange
current acquires various values in solutions of different con-
contrations; this fact is traced back to a function of the
Card 3/4 dogree of dissociation of the uranium (VI)-salts vs. the pH

The Mechanism of the Electrochemical Reactions on a SOV/76-32.--7-8/45
Mercury Cathode in Uranium Salt Solutions
,of the solution. The determinations in the second exchange
reaction showed a linear function-of the quantity of tb~e
exchange current vs. the U02+ ion concentration in the
solution; this is explained by.the influence of the electro-
chemical reduction of the tetravalent ions to trivalent ions.
on the velocity of the exchange. There are 9 fiKures, 2 tables,
and 11 references, 5 of which are Soviet.
ASSOCIATION: Fiziko-khimicheskiv institut im.L.Ya.Karpova,9oskv& (Moscow
PIVoicoebomical Institute imeni L.Ya.Karpov)
1. Mercury cathodes-Electrochemistry 2. Uranium salt solutions
ft.W-E3A'0tiochMiGtVy - 3. Uranl~m~Polal6grip*id dnilydis
4. Exchange reactions
Card 4/4

5W
AUTHORS: Rakov, A. A. , Vejq_a1a*a4Lb ~.ff sova,K.I., SOV/76-32-12-8/32
Kasatkin, E. V. 9 Boris-ova-, T. I.
TITLE: The Mechanism of the Joint Electrochemical Formation of Ozo.,e,
Persulfuric Acid and Oxygen on the Platinum Electrode
(0 mekhanizme sovmestnogo elektrokhimicheskogo obrazovaniya
ozona, nadeernoy kisloty i kisloroda na platinovom elektrode,
PERIODICAL: Zhurnal fizicheakoy khimii, 1958, Vol 32, Nr 12,
pp 2702 - 2710 (USSR)
ABSTRACT: The electrolysis is carried out in lOn sulfuric acid with a
cylindrical platinum electrode refrigerated by methyl alcohol.
Analyses of H202, H2SO5' H2S208 and ozone and measurements of
the general acid concentration were carried out in brief
intervals. Two stages were observed (at -500C and 0,5 A/cm 2
In the first stage oxygen was formed at a potential of 1,0 to
198 V, while in the second stage the potential rose to 3,0 V
resVIting in a high persulfuric acid yield and a low ozone
yield. The transition took place within I to 2 minutes. By
Card 1/2 means of a rapidly revolving platinum electrode in the

The Mechanism of the Joint Electrochemical Formation of SOV/76-32-12-8/32
Ozone, Persulfuric Acid and Oxygen on the Platinum Electrode
Dewar flask which was filled with a freezing mixture of
carbon-dioxide snow and methyl-alcohol, polarization curves
were plotted at various temperatures in 10n sulfuric acid.
Also in this case the jump in potential was noted, the curves
differing according to whether they were plotted beginning at
a low.amper'age and ending at a high one, or vice-versa. All
showed a hysteresis loop. At a temperature of -70 0C a third
stage occuried in which ozone is produced abundantly at a
potential of 5.5 to 7s.0 V. These jumps'in potential and the
chemical reactions due to them are explained by the changing
surface finish of the electrode and the influence of
intermediate platinum compounds. There are 8 figures and
19 references, 7 of which are Soviet,
ASSOCIATION: Fiziko-khimicheskiy institut im. L. Ya. Karpova Moskva
(Physico-Chemical Institute imeni L. Ya. Yarpovo Uoocow)
SUBMITTEDs July 10, 1957
Card 2/2

------- ---- *LOV31u jIT, --I.
"The Chemical Nature of CauBtobiolitbs from the viewpoint of Genesis."
report to be submitt6d for the Symposium on the Nature of Coal, Dhanbad, India,
7-9 Feb 1959-
Inst. of Mining, Acad. Sci. USSR

5m FHASX I BOOK M=ITATION SaV/2216
Soveshahanlye p0 olaktrakhlmll. 4th. Moscow. 1956.'
Trudy... i I sbornlkl (Transactions or the Fourth Conference an Elect-
rochoulatry; Collection of Articles) Moscow, Izd-vO AN USE.
1959. 86a p, Errata slip Inserted. 2",500 copies vrlnttd.
3ponvorIng Agencyi Akadamlys nauk SSSR. Otilelonlye WhIatcheskikh
nauk.
Editorial Boards A.S. Frumk1n (Reap. Rd.) A"d*ulcl". 0.A. Youln,
Proremsorl 3.1. Zhdanov (Rea Secretary?, B.S. Kabanov, Pro-
9. W
Xaba
v
of
o
N
P
R
)
no
ess
acreta"
.
r
f*aaor, 3.1. Zhdanov (
asp.
r%
l D.
.
YA. K. Kolotyrk1n, Doctor Of' Chemical Sclancovj V_V. Lonew. F.D.
Lukovt soy., Professorl Z.A. 3olov-yoval V.V. 3tander. Profosaor-.
and O.M. Florlanovich, Ed. of PublishIng Houses X.O. Yo&orav-.
7J.i T.4. :r-azakova.
PURPOSIt This book Is Intended for chemical and ol*ctrlcal ongi-
physiclats, metallurgists and r*oa&rchorb Interestisl In
ors
::
'10 "nects of electrochemistry.
um
ZZ, ::
-'CIOVT.RAaES The book contains 127 of rho 133 reports PrvSort.d at
the fourth Conference an Elect rochealstry sponsored by the Depart.
Bent Of Ch~mlc&l Sciences and the 1"ttrute of Physical Chemistry
.
Academy of Sciences. USSR. The collection pertains to different
branches 01' electrochemical kinetics. double layer theories and
galvanI4 processes In metal 61detrOGOV081tan and Induarr1mi elect
rClysl*. Abridged discussions are given at the and Of each d1v1

*Ion. The majority of raportp not Included he
-9 hava basis
published In periodical literature.
No personalities are mentioned
.
References Arm given at the end of most of, the artlclts.
Tole
jovski y6 (PIZ Iko-khimichoskl Y- jW~tji~i i7L. Y4
4-
N
--sturpov,
1
alcochamical institute Imant L. Ya. Karp*v).
Rochanism of Zlectrochemleal Illectrolyt1c) Oxidation 241
_-KAkqrs`"1-A.X'-(In'tltUt* of Sleet rochealm try, Academy or
Sclancos,USSR). Recriantsm of Oxygen Evolution at Oxide
Slactrodoo 252
J111=01-2-3 - and YG._L_%jjkov.'oVsL. Study of the Xec"nls-v
or the Electrochemical Poi;iit-nn-or Oxygen Compounds of
Chlorine by the Anode Pola.rizatlon Method 25T

__TLbOr. and I!t
('bu4-ptst -w-ettj
-
.
i9
tytv).
.
. - . .1 ..'
InrLuenvo ug- Cations on 4ygou vvervoltago 963
Transectlons of the Fourth Conference (Cent.) BOV/12216
.9rams-11'shchikov. A.X. (Gosudaretvennyy in6tttut &XOZf,3Y
promyshlonnOStI - State Institute Of the XitrO66" Industry)
Electrochemical Reactions Of 0XY&eO
,perbovich'N A (Deceased). and R.I. KaganovIch (Nzscow State
Vni,ersliyl. Study of the Kiihantaft of-Some Anode Prov "-#V*2T7
by Combining Electrochemical and Tassed-Atom Methods
Shlyg1n. A,1.. and O.A. Bogdanovaiely (Moscow State UnIveralty)
Mechanism of th*-k-lectrachealic&I OxId&t1Oft Of 31000 COPP*un~.
on ristinum 282
_XhOm kay,_v.Q.. $.a. 1kikhealsarmytolyan, and A.t-- Toullov
fSookovsk ly kn*m1kO-4ekhn0l0gCnt5k1Y inStItUt inenl
D.I. Mande I eyeva -Moscow Irstitute of Chemical Technology
I"Int D.I. Nandeleyov). mechanism or the x2ectrolytio
Oxidation or Acetone In Alkaline Solutions 287
ghomutov. N, ye. (Moscow institute of Chemical Technology $Omni
Kandel*yev). Mechanism of 30me Irrvveralble Ilwet-
Card 12A4