SCIENTIFIC ABSTRACT KOLBANOVSKIY, V.N. - KOLBASNIKOVA, A.I.

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SCIENTIFIC ABSTRACT
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PETHUSHEVSKIYj S.A.p Ave redoi KOLBANQVBQLLN.p red.; P .IATONOV red G.V.0 red.; SHAWARONOV-,M.I.p red.; SHIROKOV, M.F.v .1 VIGDOROVICHs M.I.# red* (Dialectical materialism and present-day natural ociencel materials of the All-Russian Seminar of Lecturers in Social Sciences on philosoplW problems of 1wesent-day natural sci- ence] Dialekticbeskii materializm i sovremennoe estestvozna- niel abornik materialov Vaerosaiiskogo seminars. prepodavate- lei obahchestvanny" nauk po filosofskimvoprosam sovremen- nogo eatestvoznaniia. Moskvav Izd-ro Moak, univap 1964. 403 P. (MIRA 17:7) lo Moscow. Institut povyabeniya. kwalifikataii prepodavateley obshchestyennykh nauk. Kafedra didlektichookogo i istoriche- skogo materiali=a. Bzdv,m=-~A ZILZNKO, Genrikh Iosifovioh; BLINCHBY IYp Tridell LIvovich; ZHIDMMg XsA,j nauchuyy red@; NOLBANCTSKIT9 T.V., red.; SAVOMMOO To.V,, takhnored, (Soviet technical vocational education at a now stage] Sovetakoe professionallno-tekhniaheekoe obrazovanis na novom steps. Koskya, Isd-vo Oftaids,6 1959, 47 P. (Vs6eoiwnbe obahchastvo po rasprostranonliu politicheakikh i nauohnj&h snanii. Sere2., Yllosofiiapmos32) (KIIU 12:11) (vocational edueption) SOXMI Lidiya Vasillysvna# kand.filosofensuk; NIKITIN, P,,A., redo; MRANOTMIT, V.Y,g rode; ATROSHCHMO,, L~Two~ -1,Ukha. redo W-ople of inspirins Wo*l Liudi, vdokhnovennogo trade. :Koskvao Isd-vo ftaniol* 1960. 29 p. (Tvosoiusnoo obahobostvo po raspro- stranoniiu politichookikh i nauokmykh snanlig Ger,2, filosofilas no,20), (KIRA 130) (Iffialencyl Industrial) V i N USSR/Chemical Tecbnology - Cbemica),Products and Their Application. Treatment of Jktural (Hweo and Petroleum. Motor Fuels. Lubricants, 1-13 Abet Tournalt Feferat Zhur - Dimiya, No 19, 1956o 62581 Autbart Mironov,. So I., Gall.pern) Go Do, Kolbanovskiy, Yu. A. Institutiont Neeer PXV0" %V'at' ft S V I Titlet On Temperatures of Formation and Conversion of Petroleum Original Periodicals Dokl. AN SSSR, 1955, 103., go 4) W-668 Abstracts Card 1/1 On the basis of data concerning hyfwacarbon composition bave been calculated equil.1brium tamperatureo of 32 varieties of petroleum., on the basis of vhich vas calculated the new temperature for tbese petroleum varieties vhich is -17&- Calculation of temperatures vas done according to approximte formulas for the systems cyclobexane- methylcyclopentans, metbiyl cyclohazane-athyl cyclopentane; n-baxwe-2 and 3-motbyl pwtAwes., 2,2- and 2,,3-dImetby1 butanesj n-haptane--2,2-, 2,4- and 2,3-dimetbyl pentanes, 2- and 3-methYl hexanes, 3#3-dimetbyl pentane, 2,20-trizetbyl butane, 2-stbyl pentane. KOIBANUSM -Tq*-A -d an IAVROVSKIY,,K.P. "Methods 6f Utilizing AtOA6 44ra in the Chemical Technology of Petroleum," Khim. i Tekh. Topliva, Nool, pa 7U7$ 1956 Translation 1071265' Mi" --bSER/mysiedl, Chemistry - Kifietics,'Combustion. B-9 Exploaiyes*~Tbpochmdstry. Catalysis Vt.,, No, 219 Abe Jour Rofarat 57, 38" Y-Lp'ii, Ko- lbamve~i, Aueor rAvr6vsId YU*A. Tnst- s in tituto of PetiolVgj Acadcm,of Sciences USM Title % Thc:Roltk.ofI6niz4tIoa Flotchtial in Electron Chtalysis at - Metals Oria Pub Tr. TU n-AftVAN Sms 19361 8) 92-93 Abstzact The authors: ic.-ofisider the MW of c4vorb(A gas at the surface of.a. rjetal catalyst:asa seni-con~luctor and as-, suLo that for the* smie reaction of hydrogen transferthe ratio et.murGy. of. activation. valuas E at Pt W Fd mmt U ratio of Ionization poten- be approximt'jly,.ui~ml to- Ui tials,P).0f,'these.metalso ~Yrom the known values of Ein- tho deh cenation'of pipeddine and cyclohmmne) hydro- It ydroc genation of m ac Ahyl etylmiti and cyclopropane anOL the oxidation ofiso-octane atft, tha values of E of these Card 1/2 7 139,- 5(4) SOV/2o-122-6-22/49- AUTHORS: Brodskiyj' A. Mop ~olbanoval:iy, Yu. A., Filatova, Ye. D.9 Chernyaheval' A. So TITLE: On the Radiolysis of Heptane (0 radiolize geptana) PERIODICAL; -Doklady Akademii nauk SSSR, 1958, Vol 122, Nr 6t PP 1035-io38 033R) ABSTRACT: The present paper investigates the I-radiolysis of normal heptane in the liquid phase and the radiolysis of a solution of diben.syl-dulfide in heptaao . These investigations were , carried out mainly for the following purposes: Determination of the exact,kinetion of radlolysis in the initial ranges$ determination of the.influeni:e of an interruption of irradia- tion, and determination of the exaot composition and yield of the gas within a".1wide dose-interval ( tending over m9re than _ n 3 orders of magnitude)..Diben2yl-sulf do (5-011 * 10-'4M)' was added to-the heptane for the purpose of olearing up the par- tioular feature of the behavior of aromatic sulphur compounds in the radiation field and-for the purpose of determining the influence exercised by the presence of similar additions upon Card 1/3 paraffin radiolysis. In the- case of small doses, the X-ray Ori the Radiolysia of Heptane SOV/2o-122-6-22/49 apparatus ?Yn'-o-3 9 and for larger doses Cc 6o were used as radiation'sources. In the case of small doses, direct pro- portionality,between the gas yield and the duration of radia- tion was-obeervedo Interruption of irradiation caused a synchronous interruption of gas separation. Otherwise, no "radiation hysteresis" with zespect to gas separation was observed, an assertion,~whiob is strictly true. A diagram shows the dependence of the bydrogen- and methane yield on the dose.for pure heptanelantl for a dibenzyl-aulfide solution. Dibenzyl-sulfide reduces heptane radiolysis. Nextt the frac- tion of C -C5 gas is investigated; the results of the gas analysis Ire -shown in a tablo, There follow some comments on the results obtained: 1) The nonlinear effects begin with integral doses of ev/mi and occur in all components. 2) The direct disruption of C-C bonds is of particular importance in the radiolysis of alkaneab-3) The presence of acet lene in the gaseous products of radiolyeia is pointEdout- 4~ Also the great variety of aaeous products of radiolysis is of essential importance jamong them there are comparatively many isomeric"atructures)- 5) The gaseous products of a dibenzyl- sulfide solution 'contain no hydrogen sulfide. In this case the Card 2/3 protective effect'is due to a transmission of the excitation. On the Radiolysis of Reptane SOV/2o-122-6-22/49 The authors thank So L'Xironov, Academician, and K. P. Lavrovskiyq Corresponding Member, AS USSR, for valuable~advice, and they also thank No No Faymushin for his assistance~in carrying out gas 'analyses, There are 2 figures, 2 tables, and 5 references# 4 of which are Soviet* ASSOCIATION: Inatitut nef ti Akademli nauk SSSR (Patidleda. Matittite at tbb AdadaW of, Sciences VW) PRESENTED., June 4t 1958, by So I. Mironov, Academician SUBMITTEV June 3, 1,958 Card 3/3 KOLBMTOY~~, Y. A.) TOPCIMM) A. V.) LAVRCVSKIY, K. P., FROMM, A. Y.., F6tXX-,Tl. -S-.-,--a-n-rothers. ItStudying the Hadiati.on Chem istxy of Petroleum hydrocarbons and the Annl4r.qtlnn nf* Mtf-lpnr 14ist4i A M nn In ths, Uil Prnt-aqQ4nep Trvbia+v"Y 66493 BOV/20.129-1-40/64 AUTHORS t Kolbanovskiyi' Yu* I*' Kustanoviah,.I. M., Polak, L. S., ShoherbaEoval Kmrl- '.TITLEs .119otron ParamagnetAo'Resonanoe,Sp3otra ror Some Catalysts of. Catalyst Hydrocarbon Systems~and'the.Action of y-Rays on Then PERIODICALt Doklady kkademii.neuk MRI 1959, Vol-129p fir 1, PP 145-148 (USSR) ABSTRACTt The~study of the eleotron paramaguktio resonance (spr) spectra ofcatalysts and catalyst.- hydrocarbon systems represents a now method'of,investigating catalye-ts as well as chemosorptive and o4talytio'prooesses.'. The authqrs used typical oxide catalystat such as ate appliod for oracking,'dehydrogenation, hydrogena- tion, desul-furizationp sta. processes (aluminum oxide, aluminum silicate, aluminum oxide-molybdenum oxide, CoO.Al 0 MoO 2 e~ 3 Cr 0 Al 0 activated 'by X 0 and molybdenum sulfid - The. 2 3* 2 3 2 spectra of the catalysts-investigated are discussed (Fige 1-4)- The final results are summarizods IAdependent of irradiation the adsorption of hydrooarbone on k:1203- and aluminum silicate Card 1/2 66493 BOY/20-129--l-40/64 Electron Paramagnetic Resonance Spectra for Boat) Catalysts of Catalyst Hydrocarbon Systems a.nd the Aotion,of y-Hays~on Then catalysts has but little effeot,'on their syr-spectra, Ir'radia- tion produces marked ohangesIn the syr-opectra of aluminum oxide - molybdenum oxide oatalysto containing adsorbed hydro- carbons. The temperature dependence of the concentration of centers with unpairod spine indio&.tes the existence of aotiva- tion barriers. The majority of spectra ifivestigated had no hyperfine structures the one exception being the aluminum silicate cracking catalyst after adsorption of heptans and heptene and after,irradiation. There are 4 figures and 3 Soviet references. MSOCIATIONs Iftstitut n6ftakhimiahaskago-sinteas Akademii nauk 333R (Iusti-. tute of Petroleum-chemical Synthesis of the Academy of Sciences, USSR) PRESENTED& SUBMITTEDi Oard.2/2 ............. 6/02q/60/131/00/42/071 BOO4/BOO7 L exinov 1. A. L01banovsk! AMPR8.9 TITLE: calculation of' th*-tiolds' ,of the. Radiolysis. Products of Alkaneal PERIODICAL: 'Doklady Akadomii viauk. SSSR# 1960p' Val.. 131p No* 69.ppe 1380 1362 TEXT:" The,sim-of-ths presomV paper Is the setting up,of equations for-Ahe do- termination of ~ the yield of the -various fr"tions. formed in.the radiolyeiis of alkanes, Equations (1) _ (5)_sre written downt ~vhioh represent the concentration of the,individual fractions ydrogonj~sono-olsflnssj alkause with'& analler,ant a-greater molecular weight-than the Initial subotance). A special investigation in the-linear and nonlinear part,of the radiolynis leads to equations (6) and (7). That range is defined's,* linear, in which no.products of secondary reactions as yet occUr.'As an'examplo, the fractions of n-hoptano are calculated, In the linear range the following is &5L sumed for 100 or of absorbed energy: G(ff 4-91 2) G (saturate& does, T"U*t *0 d dt*&y Prod"") . O-Tv-0 (&One- olefinse with 0 y 2. (an - number of carbon &tons in the I;itial product). For 1 ml of a-hoptano, and & dose~of 1019 0v/61 the result of the calculation for Card .1 /2 j S/020/60/135/062/026036 MOW AUTHORS: and Poluk, L. S. TITLE-~ Kinetio.Equations of Radioohemical Monomolecular Reactions not Taking a Chainlike Course PERIODICAL: Doklady Akademii nauk,SSSR, 1960, Vol'-* 135, No. 2, pP- 361-364 ,TEXT.:--In the int'roduotiont the authors note that for many reactions, which are of importance in -practice, such as-inhibit-ad radiolysis of hydrocarbons, radiolysis at large integral doe'as, neither general nor special kinetic equations exist, Thereforef they set themselve3 the task of deriving equations for variou a not chain-like-monomolecular radiochemical processes of a substance X. They assume that X has two kinds of excited states, X and X* ), and an'arbitrary. number m of modes of decomposition. The (2 authors studied: A) the range of small integral doaes (consumption of X and inhibiting'aotion of the final products are negligibly small). The Card 1/4 Kinetic Equations of Radiochomioal S/920J60/135/002/026/036 Monomolecular Reactions not,Taking a BO04/BO56 Chainlike Course following is writtendown: 1) X#?-4' el excitation byradiation: W K 1~(I) (I - differentiai-doserate in ev/CM3.aec). 2) Y.*---tX (+ hV)I dissipation and radiation: W - K21XI _(2)4 3) X* ---.vproducto of decomposition (m 2 M modes of decomposition or isomerization): W ZKi[Xj (3). For two 3 1-3 excited states one finds: A K A !3 ' IIJIMI M3 )2+K(1)3 (2)1 (2)3 (42 + M- B) The kinetics of the radiochemioal reaction with (2)3)] small inhibitory admixtures'vhioh act as "catchers" and thus as protectors. ]n/3 4) 1 X"' + B ----3,X +B* (B inhibitor) W4 -- Nlx*~- 1 [IBI I n43 is an integer. C) Radiochemioal:proose -see at t-he moan integral dose.and,with an accumulation of excitation aoceptors'A in'the r4action products, On the assumption that-A is formed from X4, and-inhibits the decomposition of (2) X one obtains; I W(2)3 d[A] /dt (10), and in consideration Card 2/4 Kinetic Equations, of Radioohemical 60/135/002/026/036 ki Boo Monomoleoular-Reaotione not,Ta ng a. 4ya 056 Chainlike Course becones equal.to of the process 5): XO) + A74A_ W3 n D) The kinetics of radio- 3 I~X] [7(2) + ~1/(K( I 7,t [A] 3 (16).- chemical reactions inhibitedby small, admizttu*es of a substance., the protective effect of whioh~. is'baesd upon its consumption.. XI+ +D --tX + IF. An equation analogous to equation (16) is obtained in which [i] is substituted by [D] . wherea: [A] -increased , with an increase in the dose, [D] decreases in the cours ofirradiation. For the-oase*in which the decojmposition probability for D* is not equal to one-.T)W-~D; D* W7 'Kill and 8) K8[DIj the value of is influenoed by the ratio /K we X8 7 without the form of the equation being changed. E) Kinetics of the monomoleoular radiochemical reaction with an addition of the substance X to a medium M which transfers the radiation enorgy to X. Additional processes occur: 9) Mwr--?M*l W9 K9j9 10) M* W K 10 0111*1 Card 3/4 Kineticiquaitiona of Radioohomical S/020/160/135/002/026/06 Monomolsoular Reactions riot Taking a B004/Bo56, Chainlike Course -11)-M*+ X-'u~x +.X*,; W WK [IM [X] n/3 and one obtains: /(K~ + , + KK .I [X] n. r/3 W K K X I [1 /3/ K )(K +K X 3 1 3 .3 3 9-11 IN 3 10 110 For K 2 .,Of n.~- 31-this.equation is identical with that derived by A. Krongauz and Kh.-Sa- Bagdasarlyan for the radiolysis of bentoyl peroxide in Ibenzene (Ref.~3).'As the relations set up by the authors are valid for-all principal kinds of monomolsoulart not ohain-like radiochemical processes* special' experiments may be carried out to study the kinetic parameterao There are 3 references-. I Soviet and 2 US, ASSOCIATION: Institut neftekhimichookogo sintata Akademii nauk SSSR (Inatitute.of Petrochemical Synthesis of the Academy of Sciences USSR) PRESENTED: June.3, 1960 by A. V. Topohiyev, Academician SUBMITTED: Juno 3, 1960 Card.4/4 3/195/61/002/001/006/0016 B101/B216 AUTHOR: Kolbanovsklyp Yu. A~ TITLE: Problems'of k1n etios and mechaiiism of radiation-chemical reactions -(Second All-Union Conference on Radiation Chemistry) PERIODICAL: Kinetika i kataliz, v. 2# nos '19 19611 154-159 TEXT:. The Vtoroye Vassoyuznoye soveshohaniye po radiatsionnoy khimii (Second All-Un.ion Conferenoo,on.Radiation.Chomistry) organized by t lie Otdeleniyo khi*icheskikh.nauk AN SSSR'(Department of Chemical Joi-ences As 'USSR) and Gosudaretvennyy komitet Soveta-Ministroy SSSR po khimii (State Committee on Chemistry of the Council of Ministers USSR), was held~ln * I, Moscow on October 10-14# 1960. Intersection sessions were maiuly devoted to general theoretical problems, all other subjects being treated in the sections: (i) Radiation effeete.on aqueous solutions;' (2) radiation ef- fects on organic substances;. (3) radiation polymerization and radiation effects on polymers; (4) radiation effects on solids; and (5) problems concerning the technique of radiation-chemical studies. The present report Card 1/8 S/195/61/002/001/006/006 Problems of kinetics and BIOI[B2i6 only mentions lectures relating Wproblems concerning the kinetics and mechanism 61 radiation-ohemical reactions. (it) intersection sessions: V. L. Tallroz-e and S. Ya. Pshezhetskiy delivered the opening lecture on !'Primary events and mechanism of some radiation-chemical reactions." M. V. Gurlyev, "'Local theory' of mass spectre.." G. K. Lavrovskaya, M. I. Markin, V. L. Talfroz*a, "Exchange.of ch&rge between clow ions and polyatomic molecules." V. V. Boldyrev, "On the mechanism of tne effect of p-tevious irradiation on therate of subsequent thermal decomposition of a solid." Kh. S. Bagdaearly" discussed energy transfer in organic systems, and suggested a scheme involving formation of a complex with charge transfer at interaction between excited and nonexcited molecules. Yu. A. Kolbanovskiy and L, Ss'Polak suggested a semiempirical formula for studying the dependence of the inhibition effect on the concentration of the admixture. Kho S. Bagdaearlyant H. S. lzrailevich, and V. A. Krongauz drew attention to the protective action of phenyl rings during radiolysis of alkyl benzenes. L. S, Pnlak and A. 3. Shcherbakova also discussed the protective action of aromatio.adiaixtures. V. I. Gusynin and V. L. Talfroze studied the quenching of Ituainescence in the system dioxane terphenyl normal C1 C9 alcohols. Section 1: Card 2/6 S/195j61/OO2/OOi/oo6/006;. Problems of kinetics anC off, B101/B216 V.~ Ve Voyevodskiy, IOUechanism of,.radiolysis of water;" P. 1. Dolin and ..B. V..Ershlers."Mechanism of.radiation-chamioal transformations In aqueous aol,utione and the two-radical model of Dyne and Kennedy (1958).' B. V. Ershler and G. G. Myasishchavat "Radiolysis of dilute solutions of B20 02! and.H202 in -water.". J. At Sharpatyy and M.. A. Prookurnin, "Radiolysis of alkaline', nitrogen-eaturated nitrate solutions." V. N. Shubin, P. 1, Dolinj.and Z.1. Krylova,studied the radiol,yois of H2-saturated aqueous 2"r 3+ solutions under.pressure. They found the Fe and Fe yields to be , H+ + - related to ther,reaction 9 + H2 # V.. S..Lapik, Z. I. FedoroviA, andA. 31. Kabakchi observed that during radiolysis of sodium nitrate soluti ons the yields of nitrite and" molecular 0, depended on the "direct action" of radiation. L. G. Bugayenko observed the same effect at reduc- ti'on of the perchlorate ion. U. A. ProskurnInp "'Radiation-chemical transformitions of organid compounds in aqueous zolution.11 In the course of*this lecture#1e mentioned the'addition of OR ion to nitrate ion observied,by.V& A. Sharpatyy and Yu. X. Molin. Ye. V. Barelko, L. I. Caid 3/8 S1195J611002100110061006 B101/B216 Problems of kinetics and. ;Kartashova, M.'A. Proskurnin,,"Role of the aqueous phase as sengitizor in radiatioh-ohemical~6xidation of benzene." This effect is much slight er in.ra4iolysis of alcohols (P. X. Xomarovp Ye. V. Barelko, M. A. Proskurnin)., Reports on ion-radicals formed by-interaction of H and OH with anions were al4o read by V. D. Orekhov, V. V. Sarayeva, A. 1. Chernova, A. V. Vannikov., A.,A.,Zanookhovat S. A. Safarovt and B. P. Bogatikcv. D. 14. Shub, V. P. Belokopytov, and V. I. Veselovskiy studied the radiation-chemical decomposition..of an 02-Baturatea potassium oxalate solution in the presence of suopehdod ZnO.. M. A.- Proskurnin, A. S. Baberkin, and N. ~P. Krushinskaya, "Radiation-ohemical transformation of aqueous CCI solution 4 in the.presenoe of catalysts." Yu. A. Kolbanovakiy, L. S. Polak, and, E. B. SILlikhter, of. an oxide-catalyot system and of hydro- carbons adsorbs d to its surface." Section 2: (A) Radiolysis of hydrc- carbons. L. S. Polak read an introauctory.report. A. M. Brodakly, P. Lavrovskiyo V. B. Titov, A. V. Topchlyevp V. Yo. Glushnev, V. D. Timofeyev, N. Ya. Chernyakf V. I. Spitsyn, I, V. Veresh,hinskiy, P. Ya. Glazunov,* 0. 0' Ryabohikovag And Go X. Sibirskaya reported on investiga- tions at higher-temperaturee. V. G. Nikollskiy,~N. Ya. Bubeng 1. M. Card 4/8 9/195/61/002/001/00~/006 ~Probleme of kinetics and B101/B216 KUstano'vioh#*N. Mo Hytovao V& -G...Berezkinp V. A. Shakhray, As To Kori:tskiy, 4.' No Shamshev, Yu* No Molin, 1. 1. Chkheidze, V. V. Voievodskiy, V. K, Yermolaysvp Ye..L. Frankevioh, and V. L. Tallroze discussed the radiolysis~of frozen and solid hydrocarbons. (B) Radiation processes In organic eyetemaq with an introduotion by No A. Bakho ff. As' Slavinskayal So A. Kamenotakayas So YaO Faheshetakiyo and Go P. Zhitneva. studied the kinetics of butane oxidation by fast electrons. V. V. Sarayeva, N. A. Bakh, and.V. .1. Dakin found that the decomposition.and oxidation of diisopropyl ether proceeded by a ohatin mechanism. Yu.~L. Khmellnitekiyp'l..I. Melekhonovat and V.'V. Nestorovskiy reportea on the oxidation of paraffin by gamma radiation. B. M. Mikhaylov and V. Go, Kiselev studied the oxidation of st.hylene and:propylens by 02 under the action of fast electrons Ro V. Dzhagat spanyant V. L Zetkint and Ye..N., Zykova-discussed their studies of sulfoxidation of n7alkenes with S02 and 0 under the action of gamma radiation. Section 31 (A) Radiation 2 polymerisation. Kh. Us lismanovIUS X41 Musayevt and R. So Tillayevs "Graft polymers of acrylonitrile on.polyvinyl chloride.,, So A. Azimovg No ~V., Kordub~, So L Slepakovap and Kh. Us Usmanov, "Graft polymers oi aoolonitrils Card 5/8 3/195/61/002/001/006/006 Problems of kinetics and,&,66 BIOI/B216 band styrene +,aarylonitrile on silk.and.Caprone.11 R. S. Klimanova V. I. Sfirenkov, and N. S. Tikhomirova, "Styrene-grafted on polyethylene... B. L. Tsetlin, S. R. Rafikovj L.I. Plotnikovat and P. Ya. Glazunovv "Polyvinyl chloridep.polyaorylonitrilet and poly.,nothyl methaorylate grafted on carbon black, Xg0t ZnOf and Bob* 1. P. Barkalov, A. A.'Barlin, V. I~. Golldanskiy, B. G. Dzantiyevp L. M..Kotova# and S. S. KuzIminap "Polymerization of acetylene hydrocarbons'*" Ye. V. Volkovap A. V. Fokin, and V. M. Belikovt IIP.olymski2ation.~of tetraflu-oro ethylene by gamma radiation." A. V. Topchiyov, 1. A. Lyashenko, N. S. Nametkin, L. S. Polak# M. P. Teterinal A. S. Felldman, and TI. I. Chernysheva, "Polymeriza- tion and copolymerization of allyl silanes.11 (B~ D,A4j:ttjmr o-ffP-+a on polymers. V. L. Karpoy and Yu. S. Lazurkin, "Problums concerning the stability of polymer materials exposed to nuclear radiation fields." Yu. D. Tovetkov, Ya. 5. Lebedev, and V. V. Voyevodskiy, "Recombination .of fluoroalkyl- and peroxide radicals in gamma-irradiated Teflon." A. G. Kiselevj M. A. Mokullskiy, and Yu. S. Lazurkin, "On epr spectra,of oriented, irradiated polyethyline.11 N. A. Slovokhotova, A. T. Koritakir, N. Ya. Buben# V. V. Bibikovt and GO V. Rudnayat I'M spectra ol' fast- electron irradiated polyethylene.0 1. M. Barkalov, V. 1. Golldanskiy, Card 6/8 8/195J61/002/001/006/06 Problems-of kinstiosland soo. BIOI/B216 B. G. Dzantiyev$ and Ye..V.. Yegorov, "A method of welding Teflon and other polymer materials by localizing the effect of radiation on the surface by means of boron compounds."' Section 4: V. I% Spitsyn, I. Ye. Mikhaylenko$ and V. V. Gromov, ",Changes of sorptive properties and rate of 'isotopic exchange in Aulfates after the addition of radioisotopes." V. B. Kazanokiy, G. B. Pariyakiy,,and V. V. Voyevodakiy ascertained the presence of atomic hydrogen on the surface of irradiated silica gel by means of spr studies. S, V,. Starodubtsev and I. M. Blaunshteyn observed a change in the magnetic pr~opertieis of BaO and CuCl under the influence of gamma radiation. I. A. Myasnikov reported on preliminary experiments regarding the use of semiconductor probes to determine the concentration of free radicals. S. M. Brekhovskikh, I. D. Tykaohinskiy, S. A. Zelentsova, I. V. Vereshohinskiy,' A. A. Revina, and A. D. Grishina prepared new types of glass which exhibit no epr spectra after irradiation, and therefore are suitable for epr studies of radicals. It is finally noted that several achievements in the field of radiation chemistry are likely to find industrial application. X. A. Bakh acted as chairman of the organizing committee of the Conference. Three papers were furnished by Card 7/8 5/020J61/136/601/032/037 B0041BO56 AUTBORS: Kolbanovskiy~ Yu. A., Polakt L. S., and Shlikhter,.E. B. TITLE: Gamma Radiolyais of n-Reptane Adsorbed on Oxide Catalysts PERIODICAL.- Doklady Akademii nauk SSSR, 1961, Vol. 136, No.1, pp.147-150- TEXT: The purpose of the present work was investigation of the particular features of radiolysis of adsorbed n-alkanes with n-heptane whose homo. geneous radiol'yeis had alrnady been thoroughly investigated (R:fs- 1 - 3)- Gamma rtidiolysis the method of which had already been describe (Refs. 6, 7) was performed by means of the follo 'wing catalysts. It Pure Al2031 II: aluminum-chromium oatalyst,:promoted with potassium oxide, 90 % A12 0 3 8 % Cr O,p 2 IlIs aluminum-molybdenum catalyst, 87 % A t 2 % K20; 1203 10 moo 3 % basic sulfates; M cobalt-aluntinum-molybdenum catalyst, 3' 79 A120Y 15-5 Y- M0039 5-5 COO, Radiolysig, at catalyst II was investigated in the case of rare surface occupation (0 K 1) as well as in Card 1/5 Gamma Radiolysis of.n-Reptane Adsorbed on S/020/61/136/00-1/032/037 Oxide CatalysU the case of adsorption of"several molecular layers. The other catalysts were investigated with monomolecular,surface coating (G.. I). Temperature during the experimentIwas about -100C in-which case heptane adsorption is reversible and chemoeo.rption does not occur. Fig. 1 shows for catalyst Il the increase AP in gas pressure with respect to 1 g heptane as depending on P, whJ.ch stands for the ratio of the electron fractions catalyst/heptane. The break in the curve corresponds to the appearance of monomolecular coating; this permits to determine the specific surface of catalysts by means of this curve. If for homogeneous radiolysis AP is set equal to unity then the following values of Prel resulted for the catalysts. Catalyst It 12-7; catalyst IIt 2.0; catalyst IM 1-7; catalyst IVt 3.6. The linear dependence of AP on P in the case of monomolecular covering proves that cnergy transfer takes place only in the monomolecular layer. Rate of radiolysis for the layers above is equal to the rate of the homogeneous process. From a paper of the authors (Ref. 6) on epr spectra of catalyst systems it is concluded that the'most active catalyst is the one whose epr spectrum during-irradiation in the presence of the hydrocarbon changes~ the least with respect to -the spectrum of the irradiated pure catalyst. Card 2/5 Gamma Radiolysis of n-He.ptane Adsorbed on B/020/61/136/001/032/037 Oxide Catalysts B004/BO5 The 4P - f(t) curve taken-by an')TT-09 (EPP-09) recorder is not linear in its first section which is attributed to impurities. The latter also are assumed to be responsible that previously irradiated catalysts were con- siderably less active. The probability of energy transfer from the catalyst to adsorbed substance is estimated on the basis of the following processes. 1) X adP---'X* (direct absorption of radiation by adsorbed substance); 2) X'---)X (deactivation proces .sea, except chemical reactions); 3) V-4 pro-. ducts of chemical reactions; 4) catalyst catalyst'; 5) catalyst osta- lyst; 6) catalyst* t X __4 ca- ' - The rates of these processes ads talyst + Xads are- W I - ki 19; W 2 w k2Lx'l w3 a k 3 V1 ; W4 - k4II; W5 - k 5LDJ; W6 k61D1Q- ED] denotes the ooncent~:ation of elementary excitations in the solid, I - radiative intensity. The following is deducedt W3 k3IG/(k2 + k 3)[kj + k4lk 6Ak5 + k60)] and for homogeneous radiolysiss Wi kj1k3I/(k2 + k3). In the cas ;e of 9 ml, W 3N - 1 + 1/(Ekl/k4)(k 5/k 6+ holds, where & stands for ihe~ratio. of absorbed radiation energy per 1 am- Card 3/5 Gamma Radiolysis of n-Heptana Adsorbed on 5/020/61/136/001/032/037 Oxide Catalysts ~BOOVBO50 heptane and catalyst#'W3N was,det4rmined experimentally; t, was calculated according to Ref. 12, ki/k4=1. Prom these data the authors estimated the probability Z of total ener gy transfer% Z k6/(k5 + k6) . The values of Z for the respective catalysts are: Is 0.41, 11: 0.032, 111: 0.026, IVs 0.073. L. V. Pisarzhevskiy and A. I. Kitaygorodskiy are mentioned in the paper. The authors thank V. V. Shchekin and A. L. Klyachko for.their collaboration, and Yu. L. Khait for his discussion. There are 2 figures, 2 tables, and 12 referenoesi 6 Soviet, 4 US, and 1 Polish. ASSOCIATIONt Institut neftekhimicheskogo air-teza Akademii nauk SSSR (Institute of Petrochemical Syrithesis of the Academy of Scienoes-USSR) PRESENTED: July 5, 1960 by-A. V..Topchiyev, Academician 1960 SUBMITTED: Card 4/5 July.5, 27256 3/090/61/139/005/006/021 0 0 2104/3201 ADTHORSo Brodskiyp As X., and Xolbanovskiy, Yu. A. TITLEs Inhibition of radiolysis PERIODICAW Akademiya nauk SSBR. Tokladyt v. 139, no. 5, 1961, 1081- 1084 VEXTs A study has been made of inhibition effects of the radiolysis of organic systems by small admixtures of impurities. These effects can be regarded as a consequence of the direct transmission of an excitation to the impurity molecules. On the basis of Fig. 11 where a molecule excited by irradiation is indicated by II, and a molecule of the inhibitor is indicated by I, the following relation io obtained for the matrix element of the effective excitation energy which corresponds to a transition of II to the ground state and to a photon-induced excitation of I without emissions eiW(1r r v Ui.*f Q0(I1(:?II))f i (ri)):r -(drj) (dr,j) (3) 'JAI i Card 5 27256 S10201611139100510061021 Inhibition of radiolysis B104/B201 This inteeral is integrated over the entire space; (J.