SCIENTIFIC ABSTRACT VASSERBERG, V.E. - VASSERMAN, V.YA.

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SCIENTIFIC ABSTRACT
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6 f h t I of hvilrocarbons and Iiii-A(W19). A 7-i"Illon chAintler for iisdatchis p% 11-1w 4,wI t1w VI 'Alf" bw CIPI'll"Mi'm ,.( 't "Ildard NAOII 6 uwd ftw the tituktim iif the ~Oo f(WIlIVA. G. M. K-4.41NM CA COWIV, tombususs towns to, "a .6' v K 4 Y; a. M. Zbb.11". T=t '4h'. ..pp. watuble for Itst 1"Y""' the field Lb Wt~tA. catalyt. uld, cmbuMin tubt. filkd -il es ules. a tc", bested pre- Is 0 ~nWpd w" pt at Pd asb " on it, then in-* ksjuaily by Wskli- Of =,%,rb,,..tinurd co-- ,d into & mo contS- owne the cs~jyvt mailitAins 2M)- a' M I h6cu can be rAiMl t0 bb. into the combustkm by fg k KOWAIPOff chamber. AMP" at" MON, of Ow ~.j-. -C - ad" A. btdn Ow - U.S.&WH Chain.. TLC Noah Umak" If k.N: 16 with 6%.NllOll ,4m The.1 004 wo in j.4''Ind Ibkv lawtkm, wwt 6 Iw.vtvndl toj A by twat &Ed Crystal d" a dgtd* Tint data (s. OP. swism an 0l MmOH OW C*H- d in A.) an: Sit -in - /a 20 = 179, 35; iff. 295 and 104, of 0 The= QUM 10 the 14= C"Jjffj'C'jwby. 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'.Y the other I.M. it Catalyst with thq hww pore". is &=MpNW by It Is' bM coan6jerable Increeft Off exiXt. an ka OW of the catalytic sc"tY tbel . . grain jw With a Ms. at Catalytic act"rity* ptimum of q low-4amp. adsol"", Dets. cd the P. ,Vim a" only of No IS. cooavqwcatl~ I-U' t 0, 'biractaimatkni catalytic w0 ty. An adequate W"M" 01 thst of the . ijecti.0 ,p. g_f_ am." dtid. M be - t "Vky - &~ of a *is* as Clow as pou'll't" to he by ad- 001 The about 0- V am arml the catalytic -t"y tion between the ndrr"m j soot[ and A-01 I - teWd by tM dtbYdmt'm C Was furtliff ]a of the activities of I mid M Is ab-t With DwOli- the rat on &W- Activilits an the saM - with 1"a WAtbO-Ir I cr- W tormw vacdcally about 10% hillb &Ovid a weak sc- -bereas call w" be thl. . 1. =bdimcIb=,tGpx'w'iOwv:, ben this volmid catalYd fortmatiou of a black C deposit- W mOH decOMP. Of was towted without ng6mmtkR- With B j;j pal that BuOH Z;--k PIO-M at & sAtW-t-y rato- Ejuolf and A-01i iga", of bdwviw of M tnwards 1 the 4 ration of it, Pam " whkb Parfait, Irr, 6wb*Uot"',Ootitbbn.A,.011--b-wh Oberefi"- iluoll not 'Metric mda". I'm Itywrr ,n react only at the outetC..'a Etolf as cmw,.!' catalytic activity *( I and Ls HCOH ladimt" that 'hrtf with their activit bke , togtoll. P.M% am Partially Chemical Abst. VOL 48 No- 9 MAY 10p 1954 General and Physical Chemistry th "t of the dinne"nsions of the 0 POtoolty and th a tY of Murning 8 h=119.6n reution. In the do. C 40" J-M-M. tran MId. on) 6, L. H. - -- T . , V. ~ " ~ - . - - - ~ , I - 7~~- ;-- , r- t c, I ~ RUAM111. A.A., akademilc; VASSMYM, V.E., kandidat khimicheakikh nauk. Catalytic chamistv.7 and chemiatry of the future. Znan.sila 31 no.2: 29-34 P 156. (XIAA 9:5) (Catalymis) 50) Z1OV/62-- Q-2-34/40 AUTHORS: Vasserberg, V. E., Balandin, A. A., Malc3imova, Y. P. TITLE: Orientation of Adsorbed Molecules in the Monomol4~-cu:ar Layer on Oxidizing Catalysts (Ob oriyentatsii adqorbirovannykh mo'-,~kul v monomolekulyarnom 3loye na okisnykh katalizatorakh) PERIODICAL: Izvestiya Akademii nauk SSSR. Otdeleniye khimicheskikh nauk, 1959, TIr 2, pp 363-365 (USSR) ABSTRACT: In the present paper the authors investigated the adsorption of the lowest saturated alcohols, from C, to C of ri-pentane 4' 1 1 and dichloro ethane by differently produced Al 0 -samplr's 2 3 and MgO-, ThO 2- and ZnO-catalysts. From the determinations of the adsorption isothermal lines at 250 it was seer, that t-e adsorption in the monomolecular layer is decreasing in the 0 H "- following order: CH 3OH '~' C2H5OH '> n-C 3H7011 > n-C H 4 9 i-C 3H7OH - i-C 4H9OH > S-C 4H9OH -7 t-C 4H9OH. The size of the elementary places occupied by the adsorbed alcohol molecuie3 on the surface depends both on the structure of the alcohol Card 1/2 and on the catalyst. It was assumed that at, moderate temperature SOV/62-59 -2 --',4 /4, 0 Orientation of Adsorbed Moleculeo in the Yonomolecular Lay(;r Cataly'sts there is also a plane orientation in addition to th,~ normal one of the adsorbed molecules (hydroxyl grouP5 are orierted towards the surface). The portion of planely is different for various alcohols and catalysts. Fov thi:3 reason it is advisable to introduce instead of thie -ctuLl Fize of the elementary place a new term, the "effective spciific place" 6 It depends on the numerical ratio of the pi-anely eff' and arallelly adsorbed molecules and is different for ona alld p the same alcohol on various catalysts. The variation of the chemical character of the catalyst ccrsiderably affects the deff* (Table). There are 1 table and 9 references, 6 of, which are Soviet. ASSOCIATION: Institut organicheskoy khimii im. N. D. Zelinskoeo Akade:::-ii nauk SSSR (Institute of Organic Chemistry imeni if. D. Zv1inskiy of the Academy of Sciences, USSR) SUBMITTED: July 15, 1958 Card 2/2 VASSERj3EMP V,E-*.;-. BAIANDIN, A*A* Elementary stages of the dehydration of alcohols on A120 catalysts. Probl. kin. i kat. 10056-362 160. (MA 14:5) 1, Institut organicheskoy khimii AN SSSR, (Alumina) (Dehydration (Chemistry)) (Alcohols) S/020/60/134/00---,/039/041XX B004/BO67 AUTHORS: Vasserberg, V. E., Balandin, A. A., Academician, and -G-e6'fg'iyevskaya,1 --T. V. TITLE: Conjugate Dehydration of Alcohols in an Adsorbed Layer ~~n Aluminum Oxide Catalysts PERIODICAL: Doklady Akademii nauk SSSR, 1960, Vol. 134, NQ. 2, pp. 371-373 TEXT: In studying the dehydration of alcohols in A1203 (Refs- 1-3) :he authors observed different reaction rates in catalysts which had been prepared in different ways. In the present paper, they examined such catalysts. No. 1: A1203 precipitated by means of NaOH at pH - 6.3; No. 2: A1203 obtained by hydrolysis of aluminum isopropylate; No. 3: precipitated from aluminate solution by means Of C02 at OOC. First, th- different activities of the catalysts in the dehydratlon r-f C2H50H 'ind 'so-C3H7OH were confirmed. Furthermore, the dehydration of isopropano] 'r the presence of ethanol was studied. Since the dehydration of isopropano', Card 1/3 0 Conjugate Dehydration of Alcohols in an S/020/60/ 134/002/039/04 1 XX Adsorbed Layer on Aluminum Oxide Catalysts B004/BO67 proceeds rapidly already at 120 - 1500C, whereas ethanol d--es not yet react at this temperature, the dehydration of isopropyl alcohol was studied on a catalyst whose surface was covered with ethanol which wa~, considered an inert substance. Furthermore, water and methanol were uaed as inert substances. The effects of these inert substances were fcj!ld be different. Water, methanol, or ethanol adsorbed in equal quantitig5 reduced the dehydration of isopropanol to a diffnrent degree, this reduction depending also on the methrd of catallyst preparation. Sincc! this could not be explained by a blocking of the catalyst surface, the auth3rs thoroughly studied the kinetics of 'he joint decomposition :f isopropanol and ethanol. First ', ethanol was adsorbed at 120 - 11503C, th~-r, isopropanol, and the pressure rise of the olefin formed was meas-arel. It was found that the pressure p coatheor - 0.6 - 0.7 mm Eg calculated fcr a 100% decomposition of isopropanol was mu--h higher (P,,,,p = .I - ,.6mm F~) and increased in the course of reaction. H-nce, the authcT3 con.lude -ha'. when ethanol and isopropanol are jointly adsorbed on the ~;ata'Ay3t, a conjugate dehydration occurs. The dehydration of ethanol was strongly Card 2/3 N- Conjugate Dehydration of Alcol-iols in an 5 '020/6,0/134/'-'?~2 Adsorbed Layer on Aluminum Oxide Catalysts B004/Bo67 accelerated (compared with that of pure ethanlol), while that of isopropanol was delayed. The authors therefore conclude that the complexe--. adsorbed on the catalyst surface are not isolated but react with neighboring molecules, and are capable of forming combined complexeu (ethanol-isopropanol and methanol-inopropanol complexes) which decoml)ose, more slowly than the isopropanol complexes. There are 3 fi,~ures and 3 references; 2 Soviet and 1 German. ASSOCIATION: Institut o- nicheskoy khimii im. N. D. Zelinskogo Akademlli nauk SSSR .natitute of OrGanic Chemistry imeni N. D. Zelinskiy of the Academy of Sciences USSR) SUBMITTED: May 17, 1960 Card 3/3 VASSERBERG# V.E.; BALANDIN,, A.A.; LEVIt G.I. Radiochemical study of the mechanism of dehydration catalysis. Part 1: Reactions of C14 -dimethyl ether with hydrocarbons. Kin i pt 2 no.1:61-65 Ja-F 161. bMIM - 34:3) 1. Institut, organicheskoy kbimii imeni N.D. ZelinBkoLo AN SSSR. (Ether) (Hydrocarbons) (Dehydratioi3(uhemistry)) S/195/61/002/003/020/027 E030/E185 AUTHORSi Levi, G.I., and Vaseserberg, V.E. TITLEi Radiochemical study of the mechanism of dehydration catalysis. II. The interaction between C14- dimethyl ether with carbonyl, or some other oxygen-containing compounds PERIODICALs Kinetika i kataliz, v.2, no-5, 1961, 758-761 TEXT,. The present paper is a continuation of previous work (Ref.l: V.E. Vasserberg, A.A. Balandin, G.I. Levi, Kinetika i kataliz, v.2, 61, 1961); both were presented at the Conference on Isotopes in Catalysis. Studies have been made of the passage of C14 from dimethylether into reaction products with ketones, aldehydes, glycols, and some complex and cyclic ethers. in the presence of an alumina catalyst at 316-320 OC and a pressure of I atm. These, and earlier results, support the hypothesis of interactions by intermediate complexes on the surface of the alumina catalyst, at high temperatures and pressures. All experimental details are the same as in the previous work (Ref.1). Earlier work Card .1/ e ~_( Radiochamical study of the S/195/61/002/005/020/027 E030/EI85 showed movement of the C14 from ethyl, isopropyl, and benzyl alcohols, but not for toluol groupings of alcoholal to see the mechanisms operative in dehydration catalysis the present work therefore extended to cover various types of carbonyl and oxygen- containing compounds, The results are given in Table 1. The activity of the products is given by the specific activity in pulse/min,mg.BaCO3 (a) and in % of the initial activity of dimethyl th r (A , which was 22000-24000 pulse/min.mg BaC03 (in experiments with complex ethers - 35% lower). Firstly, except for acetylacatone. carbonyl groups, similar to alcohols and ethers, also permit C14 to reach the second and subsidiary products in considerable activity. Secondly, acetone used as second component was separated and converted into 2,4-dihydro- pbenylhydrazone, which had considerable activity, and about 10 higher melting point than the pure unradioactive material. Thirdly, acetylacetone and 1,2-propanediol had no activity after the test at a relatively low temperature (230 OC), testifying to satisfactory efficiency in separating the initial marked Card 2/1 Lf Radiochemical study of the 5/195/61/002/005/020/027 E030/EI85 dimethylether from the resulting products. The results obtained in the present and the previous work (Ref.1) show that in the presence of an alumina catalyst an isotopic exchange takes place under conditions of dehydration catalysis. They confirm the suggestion made before, that there is an interaction between the intermediate products formed on the surface of the catalyst, giving not association products but substitution products, through radical-like complexes on the catalyst surface. Experimental results obtained not long ago agree with this (Ref.5: V.E. Vasserberg, A.A. Balandin, I.R. Davydov^,Dokl. AN SSSR, v-136, 377, 1961. Ref.6, V.E. Vasserberg, I.R. Davydova,,T,V. Georgiyevskaya, Kinetika. i kataliz, v.2, 774, 1961). This hypothesis shoulo cover a wide range of catalytic processes2 such as cracking, hydro-dehydrogenation, isomerization. etc. Two questions appear resolved. First, dioxane, although an ether with a very stable ring, can undergo isotope exchange, since the dioxane-1,2 glycol system is clearly analogous to the diethylether-ethyl alcohol system. Second, the difference in behaviour between p- and a-diketones arises Card 3/ f I Radlochemical study of the S/195/61/002/005/020/027 E03O/Ei85 because the former readily chelate, especially with lighter metals such as aluminium. The chelation destroys the surface activity, as observed,, the y-ketones chelate only with heavier netals, such as copper4 and hence retain their activity on alumina. Acknowledgments are expressed to Academician A.A. Balandin, who directed the work, and to laboratory worker A,A. Sidakova who participated in the experiments. There are I table and 6 Soviet-bloc referencess two of them Russian translations from non--Soviet-,bloc publications. ASSOCIATION: Institut organicheskoy khimii im. N.D. Zelinskogo AN SSSR (Institute of organic Chemistry imeni N.D. Zelinskiy, AS USSR) Card 4/ 41 33495 11-122t) S/195/61/ooo/005/022/027 E075/E536 AUTHORS: Vasserberg, V.E., Davydova, I.R. and Georgiyevs1(aya,T.V. TITLE: A-Ppli-C-1-ti-on-0-r-11a ra -or t Ito conversion of hydrogen to the investigation of elementary stages in heterogeneous catalytic processes PERIODICAL: Kinctilux i kataliz, v.2, rl(-).5, 1961, 773-779 TEXT: The authors for the first time used the property of free radicals to catalyse para-ortho conversion of hydrogen. This was done to establish the presence of free radicals on the catalyst surface with reactions taking place in the adsorbed layer. The first reaction investigated was dehydration of isopropylalcohol on manganese sulphate. This reaction proceeds in the adsorbed layer with a measurable velocity at 165-1800C. At 1800C the period of half-conversion T 0.5 for the decomposition is eqtial to 20 min and the energy of activation is 23 kcal/mole. It was shown that the process of dehydration in the adsorbed layer is hampered by impurities, but not to such an extent as for Al 2 03 investigated later. The method and apparatus used was described previously (Ref.18: V. E. Vasserberg, A. A. Balandin, 1. R. Davydova, Dokl. AN SSSR- 134, 377, 196o). The results show that, whilst 50% Card (ED 33495 Application of para--ortho, S/195/61/002/005/022/027 E075/E536 mixture of para- and ortho-hydrogen is not changed under the experimental conditions in the presence of the catalyst and, also, in the presence of the alcohol vnpours withotit the catalyst, 15w,, of the theoretical parn-ortho conversion is achieved wheri the alcabol vapotir is contacted with the catalyst. The second reaction investigated was dehydration of alcohol.9 on A120 Al,)O- used was obtained by passing gaseous C02 into SollittoV,f AlZN8 3) 3 at OOC and baking the precipitate at 2(10-2500C for several botirs under high vacitum. It was shown that the capacity of Al,)O 3 to produce the ortho-para conversion depends on its degree ~f hydration. The samples heated at 1300C are inactive hoth in respect of the conversion and the dehydration reactions, whereas the samples heated to 4000C catalyse both the conversion and the deby3ration reaction. A120 3 heated at 200-250'C under 1-2 x 10 -4 min Hg catalyses the dehydration, but does not produce Para-ortho conversion of hydrogen. The apparatus used was somewhat different from that described previously (Ref.18). it consisted of a circulating system capable of being evacuated to very low pressures. The circulation of hydrozen is provided by an Card 2/5 33495 Application of para-ortho 5/195/61/002/005/022/027 E075/E536 electromagnetic pump. With the aid of several stopcocks it wits possible to circulate hydrogen through the reactor, or else pass hydrogen under "once through" conditions. The alcohols could be introduced into the heated evaporator in three different ways: a) in sealed ampoules, b) directly from a test tube, and c) from an electrolytic burette joined to the neck of the evaporator. Thermal conductivity detector was used to measure the degree of ortho-para hydrogen conversion (the resistance of the tungsten wire used was 60 Ohm at -196'C, 60 mA current and 50 mm hydrogen pressure). The resistance changes due to formation of para- hydrogen were of the order of 3.5 Ohm which could be easily measured with 1-2% precision. The detector was calibrated by passing through the apparatus known mixtures of para- and ortho- hydrogen produced by passing the 50YS mixtur-3 through activated charcoal. It was found that with isopropyl alcohol the para- ortho conversion reaches 25% of theoretical value, thus demoristra- ting the formation of free radicals, Results of experiments with tert-butyl alcohols indicated that the para-ortho conversion almost does not take place. This was contrary to the expected increased conversion, in view of the reported (Ref.21:B.A.Dolgoplod-c, Card 3/5 33495 Application of para-ortho S/195/61/002/005/022/027 9075/E536 B. L. Yerusalimskiy, V. A. Kroll, Sb.Voprosy khimicheskoy kinetika, kataliza i reaktsionnoy sposobnosti, Izd-vo AN SSSR, 1955, P-810) relatively high stability of tert-butyl free radicals in the liquid phase. On the other hand the dehydration of diethyl ether was accompanied by a marked para-ortho conversion (13*,,, theoretical). The second admission of ethyl ether did not produce any ortho- para conversion, but when the temperature of the reactor was raised by 200C (thus producing a partial desorption of water and regeneration of active sites) the dehydrogenation proceeded again with the accompanying para-ortho conversion (8.5&,'-' theoretical). The authors explain the differences between the properties of the adsorbed C2 and tert-C- radicals in the dehydration reaction, by inability of the latte? radicals in the adsorbed state to catalyse the ortho-para conversion. The adsorbed C 2 radicals do not loose this ability. The author conclude that for the first time they have proved directly the formation of intermediate structures possessing paramagnetic properties common to free radicals tinder conditions of heterogeneous catalysis, The aiithors believe that the formation of free radicals shotild take place for other Card 4/5 33495 Application of para-ortho ... S/195/61/002/005/022/027 E075/E536 heterogeneous reactions such as isomerisation, polymerisation, disproportionation etc. Acknowledgments are expressed to Academician A. A. Balandin for interest in this work and to S. L. Kiperman for supplying the apparatus used in the first part of this work. There are 3 figures, 2 tables and 22 references: 19 Soviet-bloc and 3 non-Soviet-bloc. ASSOCIATION: Institut organicheskoy khimii imeni N. D. Zelinskogo AN SSSR (Institute of Organic Chemistry imeni N. D. Zelinskiy AS USSR) Card 515 V-R VASSERBERG, V.Z.; BALANDIN, A.A.; MAKSIMOVA, M.P. (Moskva) Adsorption of lower aliphatic alcohols on alumina catal7sts 'and the orientation of the adsorbed molecules. Zhur. fiz. khim. 35 ~ao. 4:858-866 Ap 161s (MIRA 14:5) 1. 0 SSSR, Institut organicheskoy khimii im. N.D.Zelinskogo. (Alcohols) (Adsorption) 89617 S102 611136/002/0206/034 o I 2,1D B004YB056 AUTHORSs Nazzerh Balandin, A. A., Academician, and Davydova, I. R. TITLEt Formation of Radical-like Intermediary Forms of Surfaces in Heterogeneous Catalysis PERIODICAM Doklady Akademii nauk SSSR, 1961, Vol. 136, 11o. 2, pp. 377 380 TEXTs The formation of free radicals on the surface of catalysts is dealt with. The experimental material (Refs. 1-14) led many researchers to the assumption that heterogeneous catalysis takes place with the participation of free radicals loosely bound to the catalyst. However, no experimental proof has hitherto been obtained. To supply this proof, the reaction of isopropanol dehydration was chosen, because it takes place at low temperatures in the adsorbed layer, and thus the lifetime of the radical-like complexes could be expected to be longer than at high temperatures. As such complexes are characterized by unpaired electrons, the method was based upon proving their paramagnetism which accelerates Card 1/5 89617 A Formation of Radical-'like Inte:,msdiazy S102016,11-1,6100210261034 Forms of Surfaces in Heterogeneous Catalysis B000056 the para-ortho transformation of hydrogen. In selecting the suitable catalyst, such were not found to be eligible as, like A] 203Y were them- selves active catalysts of p-o transformation. MgSO 4 was chosen as a catalyst of alcohol dehydration, because the lattex does not activate the p-o transformation below 3000C, and thus does not produce any effect on this transformation at the dehydratton temperature (1111,0-1800C). For each experiment, fresh MgSO4 was used, because a regeneration could not be S in hydrogen at 7000C). A con- carried out (reduction and formation of H. tinuous-flow glass device was used foT the purp:)se. Thejatalyst in- stalled in it was annealed at 3000C for 3 hours at 1.10 5 mm Hg. Before each experiment, the question was examined as to whether the zatalyst itself did not bring about the p-o transformation. For this purpose, a mixture of 50 para- and ortho-hydrogen was in each case made to circulate at the temperature of dehydration in the apparatus, and samples were periodically taken, whose thermal conductivity was examined. For this pur ose, a test tube made of molybdenum glass with a tungsten wire (d - 20p~, wh'ich had a resistance of 300 ohms at room temperature, was used. Card 2/5 89617 Formation of Radical-like Intermediary Forms S/020/61/176/OG-2/026/034 of Surfaces in Heterogeneous Catalys.19 B004/Bo56 Thereupon, evacuation was carried out to 1.10-5 mm Hg, and the ampoule with i-C H70H was smashed by means of an electromagnet. All proct'lone'l were carried Lt under exclusion of oxygen which was also paramtq;netic. A3 soon as the alcohol had evaporated and been adsorbed, a cO~j' mixture of p- and o-H2 was introduced, and after 10-15 min samples were talren for determin- ing thermal conductivity. After the experiment had been completed, evacuation to 1.1o-5 mm Hg again followed, and the inactivity of the catalyst alone with respect to p-o transformation was again tested with 50% p- and o-H2' Experimental results are given in Table 1. The following results'wexe ob 'taineds 1) The 50% p- and o-H2 mixture undergoes no change in contact with the catalyst, with the vapors of the reaction products and of the alcohol in the absence of a catalyst. 2) In contact with the catalyst, on which the dehydration of the alcohol is carried out, a p-o transformation occurs, which attains 13-5%. This result is considered to be a direct proof of the formation of multiplet complexes with para- magnetic properties. The formation of such complexes is assumed also for other heterogeneous catalytic reactions. Proof is, however, rendered Card 3/5 89617 Formation of Radical-like Intermediary Forma 3/020/61/1.-6/002/026/034 of Surfaces in Heterogeneous Catalysis B004/BO56 difficult by the authors' method because all catalysts used for hydro- genation and dphydrogenation catalyzed the p-o transformation of H2 them- selves but, in the case of catalytic oxidation, paramagnetic oxygen disturbs. Mention is made of N. D. Zelinakiy, V. V. Voyevodskiy, F. F. Vollkenshteyn, N. 14. Semenov, Ya. T. EyduB, S. Z. Roginskiy, M. I. Temkin, and S. L. Kiperman. There are I figure, I table, and 17 references: 15 Soviet, 1 Belgian, and I German. -ASSOCIATIONt Institut organicheakoy khimii im. N. D. Zelinskogo Akademii nauk SSSR (institute of Organic Chemistry imen-' N. D. Zelinskiy of the Academy of Sciences USSR) SUBMITTEDt August 30, 1960 Legend to Table It a) Number of experiment; b) quantity of catalyst, g; c) temperature, OC; d) quantity of initial alcohol, ml; e) duration of circulation, min; f) degree of ortho-para transformation; C) infinite. Card 4/5 Formation of Radical-like IntemediaI7 FOMB of Surfaces in Heterogeneous CAtA,)jviB r& 1* 4 OnuTa IC A 1 0 180 O,i 6eCKOH. 0 2 0 200 0.4 0 0 3 3,3 156 0,0 9 01 3.3 156 0.05 15 13.3 3.3 156 005 6CCKOH. )13,3 4 10,7 185 0:0 6 0 10,7 185 0,4 15 13.5 10,7 185 0,4 6ecgou.. ) 13,5 5 it 0 187 0,0 1 0 11:0 187 0.2 15 513 11,0 187 0.2 6ecxoR. i) 5.3 6 It,O 183 0 0 11,0 183 0.4 15 13,2 11,0 183 0,4 16CCKOH, 11 13.2 Card.5/5- 89617 B/02o/61/136/002/026/034 B004/Bo56 VASSERBERG-, V.E.; VALANDIN, A.A., akademik; GEORGIYEVSKAYA, T.V, Reciprocal effect of reacting molecules at the surface of dehydration catalysts. Dokl. 'AUN SSSR 14C no.4:8,c9-862 0 '61. (MIRA 14:9) 1. Institut organicheskoy khimii im. N.D.Zelitiskogo AN SSOSR. (Dehydration) (Catalysts) VASSERBM, V.E.; BAUTMIN, A.A. , akademik; G:EO'1TjIYZVSK:tYA, T.V. Inhibition of surface reactiors on catalysts of absorbed noleev.1ev. Dokl. All SSSR 1. Institut organicheskoy Yhimii im. (Dehydration) (Catalysts) (Adsorption) and the mobility 140 no.5M10-1,1-13 0 161. (I-aRA 15:2) N.D.Ze2inskogo All SSSR. PAVLOV2 Boris Alekseyevich; 11904T'YEV, Aleksandr Petrovich, prof.; - VASSERBERG, V.E., red.; LURIYE, M.S., tekhn. red. (Course in organic chemistry]Kurs organicheskoi khimii. Izd.4. stereotipnoe, ispr. Moslcva, Goskhimizdat,, 1962. 592 p. (MI.U 15: 10) (Chemistry, Organic) VASSERUM., V.E.; HALANDIM, A.A.; 14MIMVA, M.P. Geometric configuration of adsorbate molecalos and the dizensiots of elementary surface aCeas in the adsorption layer. Izv. AN SSSR.Otd.khim. nauk no.10:1865-18V-.0 162. (MIRA 15:10) 1. Institut organicheakoy khimii im. V.D.Zelinskogo AN SSSR. (Adsorption) LEVI, G.I.; VASSERMR~C,_.~.E. Recirculating catalytic apparatus. Kin.i kat. 3 no.4:527-528 Jl-Ag '62. (KRA 15:8) 1. Institut organicheskoy khimii imeni N.D.Zelinskogo AN SSSR. (Catalysis) (Chemical reactors) VASSERBERG, V.9. standardization and automation of certain laboratory processes for the preparation and inyestigation of catalysts. Kin.i kat. 3 no.4:556-564 Jl-Ag 162. (NIRA 15:8) 1. Institut organicheskoy khimii AN SSSR i Laboratoriya imeni N.D.Zelinskogo. (Catalysts) S/062/63/000/001/003/025 .B100186 AUTHORS: Mlaksimova, M. P. , and Balandin, A. A. TITLE: Effect of the degree of dehydration of the A12 03 surface on its adsorptive properties and on the elementary area of the molecules adsorbed PERIODICAL: Akademiya nauk SSSR. Izvestiya- Otdeleniye khimicheskikh nauk, no. 1, 1963, 17-21 TEXT: The elementary area o populated.by an adsorbed Ar atom or N 21 C iD 1.] 2H5OH, n-C 5H12 or C611 12 molecules was determined in Al 2 03 samples calcined at 3000C (sample 1) up to 10000C (sample IV). The adsorption of Ar and N 2 was measured at -1950C, that of the organic compounds at 250C- 0 Ar was assumed constant at all temperatures,and e4ual to 16.6 ~2. ~2 - values found for sample I: cj N2 - 17.2; ~-,C2115off 28.2; -,-) n-C5H12 " 54.2; Card 1/3 s/c,62J63/coo/cci 1~,;31102:; Effect of the degree of B101/B166 G)C6 H12 w54.5; for sample IV: 15; 24 .-3; 46-5 and 44-5, respectively. 0N was almost constant for all Al 20 3 samples heated to more than 300 0C. Conclusions: The determination of the specific area of Al 203 catalysts by 142adsorption is not affected by the degree of surface dehydration. The slight changes of do not explain the previously observed C 2H5OH (Zh. fiz. khimii, 35, 858 (1961)) laree differences of (,) when alcohol was adsorbed on Al 203 samples of various origin, which were dehydrated at 5000C. The reduction of cj C2H 5Oil with increasing dehydration may be explained by formation of highly active oxygen bridges between the aluminum atoms in intensely calcined samples. The (J'of the two hydrocarbons varieb between physical values. The anomalous increase of C.) observed by 1-1. M. Dubinin (Izv. 0 SSSR, Otd. khizi. n. 196o, 1739) in fluorized silicagela was not observed with Al 203 0'although interaction Card 2/3 Effect of the degree of SIC6 63/000/001/003/025 B101yalb6 between the molecules of the adsorbate is equally possible. Hence, the BET (Brunnauer, Emmett, and Teller) equations can be used for Al 20 3as its surface is only slightly inhomogeneous. There are 1 figure and 2 tables. The most important 'English-language reference is: I. B. Peri, R. B. Hannan, J. Phys. Chem., 64,.1526 (196o).' ASSOCIATION: Institut organicheakoy khimii im. 11. D. Zolinskogo Akademii nauk SSSR (Institute of Organic Chemistry imeni N. D, Zelinskiy of the Academy of Sciences USSR) S~BYITTED: April 23, 1962 Card 3/3 - VAS SERBEFiGi V. Ye. "Interaction between adsorted molecules and the mechanism of the elementax-y ar-ts in the dehydratioa of alcohols on oxide catalysts." report submitted to 3rd Intl Cong on Catalysis, Amsterdam) 20-25 Jul 64. Inst of Organic Chemistry im Zelinskiy, AS USSR, Moscow. SubJect USSR/Electronics Card 1/1 Pub. 89 - 14/118 Author Title Periodical Abstract AID P - 4947 Vasserman, A. Calculation of chokes for fluorescent lamps Radio, 8, 44-45, Ag 1956 The author explains the principles of operation of a fluorescent lamp, and gives a simple method of calculating ballast chokes for this lamp. Three drawings, 1 table. Institution None Submitted No date I ~ I AUTHOR: Vasserman, A. SOV- 10 T-Vi -I - ------------ TITLE:; A System for the Starterless Ignition of Tub,:s (13owif"Ir."orwlyri J~hfnjjtt ztj-,hjganjya PERIODICALs Radio; 1958, Nr 4 P 44 (USSR) ABSTRACT, A scheme for the 3WJ. rt 4gnit;on of 11=ines~en' 111b(- out using a starter is described. It is bas9d cn the us2 of a tapped filament transformer to heat the -athnies ar,2 at the same time supply the voltage. A conductive plat's fitted to the glass envelope-of the tube further aids igr-:- tion and the period required is cut from 15 oeconins a starter) to 1-2 seconds. Transformer winding data -'s given. There is 1 circuit diagram and I table. 1. Discharge tube heaters--Design 2. Discharge tubes--Equipment C a r d I UESSEW A. inshener-konstruktor. Graphic method of calibrating the cutoff valve frase on a Iteam engine. Mor.flot 16 no.4:26-27 Ap'56. ~nu 9:8) 1. Rishokiy sudoetroitelln"-sudoremoutnyy sayod. (Boilers, Karin*) VASSEM-Wil A. A.; RiWINOVICH, V. A. "Calculation of the viscosity and the thermal conductivity of air and its components for wide range of Earameters." report submitted for 2nd All-Union Conf on Heat & Mass Transfer, Minsk, 4-12 may 1964. Odessa Inst of Naval Engineers. STAROSELISKIYq A.A.9 dotsentp kand.tekhn.nauk; VASSMIANq A.A.9 inzh. SMMOV o V. S. 9 inzh. Results of endurance testing of piston rings of diesel engines. Vest. mash'. 41 no.3:11-15 Mr 161. (MIn .14:3 (Piston rings-Testing) VA.53ERK&N, A-A., KAZAVCHINSKIT. Ta.Z. Equat ion of a tate f or air. Insh. -f ix. zhur. no.4:81-84 Ap 160. (XIU 13:8) 1. Institut inzhenerov morskogo flota, Odessa. (Air) (Eqaation of state) VASSElftill, A.A. ; &LIKIOR, K.A. Apparatus for determining the wear of cylindrical bushings by the mnthod of impressions. Zav.lab. 26 no.8:1026-1027 160. (MIRA 13:10) 1. Odesskiy Institut inzhonerov morskogo flota. (Testing machines) ZAGORUCHENKOI V.A~3 VASSEPMANY A.A. Equation of state and the thermodynamic propert�es of methane, Inz- fiz.zht=. 4 no.11:59-63 N 161. (XIRA 14:1""1"' 1, Institut inzhenerov morskogo flota, g. Odessa. (Equation of state) (Methane. .-Thermal properties) 5/1 52/61/000/004/00~/"j~j.; B 126/B219 AUTHORSt Vasserman, A. A., Zagoruchenko, V. A. TITLEt The thermodynamic properties of natural gases in the state of a perfect gas PERIODICALs Izvestiya vysshikh uchebnykh zavedeniy. Neft' i gaz, no. 4, 1961, 69-72 TEXT: For various technical calculations in connection with natural gases. exact data on their thermodynamic properties are required, which in generai are obtainabl.-) only from the values of a perfect gas. For the temperature interval -100 to +3000C, which is important for practice, the authors established equations for the molecular heat capacities/4c Po of the natural-gas components that possess the properties of a perfect gas, and calculated from those the thermodynamic properties of natural gas from three deposits. The highest accuracy was achieved with equation (1), /1cpo - a + bT + cT2 + dT3 , where TOK - tOC + 273-15- In the following Card 1/4 S/152/61/000/004/005/009 V The thermodynamic properties ... BI,16/B219 Table 1, the coefficie:.'.-s of Eq. (1) are given for seven basic components of the natural gases. Tiahla I Coefficients CH 4 CA C3H8 C4H 10 5H12 N2 C02 a 2 9.8417 8.8173 11-1479 10-7781 13.2065 .9362 4-97Y3 b-10 -2.2643 -1-1312 -1.8102 1.4592 1.9960 0.0275 1.5192 C-104 0.7725 1.0713 1.8039 1.3257 1-5949 -0.0163 -0.0696 6 d-10 -0-05350 -0.09004 1-o.16070 1- 0.12557 1 -0-15290 0-0031T L 0.0015 From the data of Table 1 and from the percentage by volume r i of the natural gases from three deposits (Table 2), equations for the molecular heat capacities of these gases were obtained according to formula (2) /to PO 'Z/.,,Po,*r,, Card 2/4 S/152/61/000/004/005/009 The thermodynamic properties... B126/B219 Table 2 ------ U., -.0. frnm fhT-PP dPnnRitR2 no. of deposit CH L C2H6 C3H8 C4HjO C5'121 11 -2 CO2 1- 92.9 0 0.5 0 5 0.09 0.01 2 96.6 4 70. 0.14 m6 0.7 0-1 3 97.6 0. 3 0.2 0.1 0.1 1.5 0.2 temperaLre portion of the The values of the enthalpy, i 0, and the entropy, a 0, for the mentioned substances were calculated by the equations for their molecular heat capacities /4c PO and by the known relationst at 10. f cPo dT + const (3) aT- ~cpo dT + const (4). 0 T The constants of integration were calculated from the conditions that T 0 io - 0 and a 0 . 0 at t - -100 C. The thermodynamic properties of the Card 3/4 S/152/61/000/004/005/009 The thermodynamic properties ... B126/B219 natural gases of other deposits can also be calculated from the data in Table 1. There are 3 tables and 17 referencess 4 Soviet-bloc and V/ 13 non-Soviet-bloc. The two references to English language publications read as followst Hilsenrath J., Tables of Thermal Properties of Gases, NBS, Circ, 564, 1955; Kobe K. A., Long E. G.,Petroleum Refiner, 28, 113, 1949, ASSOCIATION: Odesskiy institut inzhenerov morskogo flota (Odessa Institute of Engineers of Naval Forces) SUBMITTED: December 15, 1960 Card 4/4 VASSERMAN, A.A.; MASYUK, S.P. Investigating the shape of pyramidal impressi-;ns on cast iron under various loads. Zav.lab. 27 no.8:1028-1029 '61. (MIRA 14: 7) 1. Odesskiy institut inzhenerov morskogo flota. (Cast iron--Testing) VASSEFaM A. A. Effect of the elastic recovery of izpressions In heating on the results of testing cast iron for weare Zav. lab. 28 no.12: 1490-V,91- '62. (M RA 16 % 1) 1. Odeaskiy institut inzhenerov morskogo flota. (Cast iron-Testing) VASSERMAN-,-A.A.; ZAGORUCHENKO, V.A.; KAZAVCHINSKlY, Ya.Z. Equation of state for methane - ethane mixtures. Zh-,=. fiz. khim. 36 no.11:2527-2529 N162. (MIRA 17:5) 1. Odesskiy institut inzhenerov morskogo, flota. D c t c Vyj. STAROSELISKIY., A.A. . dotsent; SE,-ENOV,, V.S., kand.teklin.nauk; Y4~~EILM-Alijy A.A. , inzh. Interrelationship between elements of cast-iron friction pairs. Izv,vysoucheb.zav.; mashinostr. no.8:128-132 163. (MIRA 16:11) 1. Odesskiy institut inzhenerov morskogo flota. VASSERMAN, A.A., inzh. Themodynam.ic properties of air a' temperatures up to !0000 C 6 and presaures up to 1000 bar. Teploenergetika 10 no..U:81-85 N 163. (MIRA 17: 1) 1. Odesskiy institut inzbenerov morskogo flota. jr ACCESSION IM: AP403866z S/0170/64/000/OC4/0044/0050 AUTHOR3 -Vassoman.,A. As; Rabinovich, V. A. TITLE: On the problem or calculating the viscosity of real gases SOURCE: Inzhonerno-fizichoskiy zhurnal, no. 4. 1964, 44-50 TOPIC TAGS: Real gas viscosity, dynamic gas viscosity, gas viscosity calcula- tion, air viscosity calculation, bxcess real gas viscosity ABSTRACT: The article shows the desirability of using the equation of state of a real gas represented by elementary functions for calculating the viscosity over a wide range of parameter variations by means of an equation derived by I. G. Golubov. An equation was formulated for the viscosity of air, and calcula- OOC and pressures of tions were made for temperatures in the range of 0 to 100 (1-1000) 10 n/mZ. Calculated and experimental data on the viscosity of air in the range of 0 to 1500C and values of the coefficient of dynamic viscosity of air for the 0-10000C range are tabulated. Origs art. has.2figuroa, 5 formulas, and 2 tables. !'Card 1/2 ACCESSION NR: 'Ap4o)86U ASSOCIATIONt tut iukhon,,roy morskogo flota Engineers) Odexes, (inatitute of Naval SURaTrEDI Mugg63 DATE ACQ3 19may64' SUB COM No REF SOVI 006 ENCL, 00 ODM 1 003 C.,d 2/2 V A PIMP. 11 , I'. , il. ': A l ,f n --rove n alnd Cx7ger, ~n t~-e a a --urc- *.,~-,- , ~, - I I - f, ~ -.- ~-, -, s '~ at 4- F4, ., nz- . '-, z, Z., III T 4 '1 n, f - Pr', 91 164, , Y - . -.1, 1. -ILnslv.',.t,,!t lnzhere-zov morskogz) ficta, Odessa. L'23052-65 BIT (1)ISUT (-Ai)/EPF (c) /FPFt Pr-h/Ps-4 RPL W'vl/,tw/JD ACCESSION NR: AP4047979 S/0076164/0381010/2386/2391 AUTHOR: Vasserman, A, A. (odesa) TITLE: Eguation of state for nitrqgpp~~ SOURCE: Zhurnal fizicheskoy khimii, v, 38, no. 10, 1964, 2386- 2391 TOPIC TAGS: nitrogen, equation of state ABSTRACT: Aji ~~qqgion of state for nitrogen was derived in which the compres- sibility at reduced densities from =0 to 2. 8 from the saturation curve to' 1000C was described with a high degree of precision: cr = aa + al'r + pip + IV, d=pv/RTk,%=T/Th,w=pipj.,Tt.=126,25*K.pi,-0,2952 I? = 290,77 Card 1/ 3 L 23052-65 ACCESSION NR: AP4047979 + A_ rn .0 Coefficients of the elementary functions are given in the enclosed table, The e- quation satisfies the critical point, critical conditions and Maxwell's rule, and reliably represents Boyle's curve, the ideal gas curve and the inversion curve, The S-shape of the subcritical isotherms of the general equation of state is deter- mined not by the degree Of the equation but by the presence of metastable states in the substance. Orik,. art. has: 4 figures, 3 tables and 2 equations. AS --- SOCIATION: Odesskly inatitut inzhenerov morskogo flota (Odesfia Institute of Merchant Marine Eilgineers) SUBMITTED- 10Oct63 ENCL: 01 SUB CODE: IC, GC NO REF SOV: 007 OTHER: 025 c.,d 2/3 L 23052-65 ACOMIM IIRSAP4047979 01 0 I 0,401,A-', 0.31G582 -1.814524 1) 3,27M) 3. GMOO 3,261570 _A '444-143 0,15OGM 0 3,39407b -5,01:40.1 -7, 153137 -5,187.111 3 7,844H26 _ 0,M16 2,103310 -0,261376 6,07272 7,881485 4.642341 1 -5 710725 0 714054 9,745213 -4.69W% --3,(*4,t47 -4,416M -2,084U0 ff 3:mmc!,1s -0:343053 tt,?A25f4 8,05"F47 0.593120 0. GO 1130 0. 372M 0 -1,5031a 0,070064 . 4 3535813 -3,77WJR 7 0.584359 --0,005217 - 0:577354 0, 5353981 8 -0, 139,577 9 0,013706 (;ard 3 3 L 24169-65 EWT(1)/6WT(m)/EPF(c)/EPa/ZWP(t)/i:WP(b) Pr-4/Ps-4 IJP(c) ACCESSION NR: AP5002579 JD S/0076/64/038/012/2942/2946 AUTHOR: Vassennan A.A.(Odeoua) S :m apLic I era in the supercritical moon "ITLE: The t4~~t .p!~ __qtabi ity of nitrom SOURCE: Zhurnal fizicheskoy khiinfl, v. 38, ao. 12, 1964, 2942-2946 TOPIC TAGS: nitrogen, nitrogen stability, vapor pressure. quasispinodal, supercritical region, isothermal compreseion -A-B5TRACT.--- Th.- Enerrnodynasrnlc~stab.fllty of nitrogen in-the-supe -criticalregion-was- y calculated and the qua-Malsinodal was shown W infersect the bifiodrd ai 'he re-diwPd -1 and f' 9~1 n-M4,f tho qp~-; n of th4 staide reg-ion whpi-e. i.14 1 -7A F -I - 1 Card 1/3 L 2416)-1-9 ACCESSION IiR- AP5002579 A CC;, 1,1' 1 ~ 'r T ( ) \T . , , : ; , , L: ;c tf r SUBMITTED- 100ct63 ENCL: 01 SUB CODE: GC NO REF SOV- 022 OTH ER.- 004 2A L 24169-65, ACCESSION NR: AP5002579 bar Qt -Q - Fig. 1. Quaaispinodal of nitrogen (do' ed line) and the vapor pressure curve (solid lille) tt Cnrd 3/3 1. 32008-66 .__ Fdr-(i)/zwr(m)/TZ.F&P( AMN-Er" *MP60lL62 SOURCE CODE: UR/0115/66/000/00310~j77/--jl!(I IAUTHOR: Vasserman, A. Al.,;-Rabinovich, V. A. 1ORG: none i t/ iTITLE: Thermodynamic Rroperties of nitrogen up to 1300*K and 1000 bar ISOURCE: Izmeritellnaya te'khnika, no. 3, 196, 77-80 TOPIC TAGS: thermodynamic property, enthalpy, entropy, nitrogen ABSTRACT: Tables of the most important themodynamic properties of nitrogen are dis- cussed. On the basis of extensive references, tables of specific volume, enthalpy,,en- tropy and heat capacity covering temperature range from 2500K to 13000K ar~d-pr~`ssure range from 1.0 to 1000 bars, have been compiled. In addition, some computed values are also given and their relationship to experimental data is discussed. Some of the methods used in obtaining the values in the tables are discussed and error estimates are made. 'On the basis of agreement between computed values and values measured by many workers, the tables are recommended by the authors as sufficiently accurate for en- gineering work in the relevant temperature and pressure ranges. Orig. art. has: 6 tables. SUB CODE: 20/ A ORIG REF: 006/ SUPM bATM: -AMXP- Card OTH REF: 018 UDC: 546.17(083.3) ACC NRs tm60367~15 Monograph UH/ Vaq~~rTsjj, Aleksandr Anntollyevich; Kaznwhinskiy, Ynkov 7.mkhRrovich; Rabinovich, --Viktor Miihmb-i1-ih' Thermophysiam). propertieu of air and its components (Teplofizichenkiye avoystva vozdahn i yego komponentov) Moscow. Izd-vo "Nauke. 1966. 374 p. biblio. dingr. , (4 in pocket).. Ubles. (At head of title: Akademi-ya. nauk SSSR) Errets slip inzerted. 3400 copies printed. TOPIC TAGS: air.. thermal property, thermodynemic analysis, thermodynamic function,, power plent,ges property, gas dynamics, gas viscosity PURPOSE AND COVERAGE: This book in intended for scientists, designers,, engineers# teclipicians, and students engaged in research, design, and study of thermal power In4tolletions and the separation of gases from a gas mixture. This book presents a method for setting up an equation with which to define the state of ffn actual gas by means of elementary functions derived from experimental thermal date. The resultant equations are sufficiently accurate to be used for determining thermal and caloric valuen. Such Values were determined for air, nitrogen, oxygen, and argonp and their thermodynamic characteristics dots have been arranged in tabular form. Diagrams indicating the state of each substance are also given. Experimental data on the viscosity and heat conductivity of air and its components are analyzed and inferences are drawn, The authors ex- press gratitude to A. Ye. Sheyndlin, V. 1. Yeplfenove and V. I, Nikolayev for Cwd 1/2 Me: 546.217 their advice. There are 65 references, 20 of vhich am Soviet. TABLE OF CONrWM (Abridged] introdUctIon -- 3 Key to the symbols used In tables I--XXI -- 5 Ch. I;.. Analytical description of experimental data on thenmal properties of actual gases -- 6 Ch. 2. Thermodynamic properties of nitrogen -- 39 Ch. 3. Thermodynamic properties of oxygen -- 106 Ch. 4. Thermod~mamic properties of argon.-- 159 Ch. 5. Thermodynamic properties of air -- 206 Ch. 6. Tenacity of air and Its components -- 2T4 Ch. 7, Thermal conductivity of air and its components -- 322 SUB CODE: 20/ SUM DATE: 3ONey66/ MIG MW: 156/ OM MW; 264 Cwd 2/2 ACC NRI AT7000961 SOURCE CODE: UR/0000/66/000/000/0090/0097 AUTHOR: Vasserman. A. A.; Rabinovich, V. A. ORG: Odessa Institute of Naval Engineers (Odesskiy Institut Inzbenerov Morskogo Flota) TITIZ: Thermal conductivity of air in the 0-10000C interval and pressures below 400 bar SOURCE: AN UkrSSR. Teplofizicheskiye svoystva veshchestv (Thermophysical properties of materials). Kiev, Izd-vo Naukova dunka, 1966, 90-97 TOPIC TAGS: heat transfer rate, heat conductivity, pressure effect, air ABSTRACT: On the basis of the previously published data the article shows the calcu- lations of the thermal conductivity of air up to 10009C and 400 bar pressure. An equation which best jescribes the themal conductivity of air as a function of pres- sure and.temperatul~e is as follows: Xp.r + 263.8. 10-4exp Ckj/m.-sec-deO wherfs XP'2' is the thermal conductivity as a function of temparature and pressure, I T Card 1/2 ACC NRt* AT7000961 is the thermal conductivity of air at pressure equal to one dyne/cm2 and a is the density of air. In general the values of Ap,T calculated by means of this equation agree with the experimental values within 12% and only along the 2000C isotherm and p = 300 bar does the maximum discrepancy reach -3.7%. On the basis of the relation- ship from the kinetic theory of gases which relates the thermal conductivity to visco-i sity and heat capacity at constant volume, the validity of thermal conductivity at higher pressures was verified. Due to the absence of experimental data, the calcula- tions of thermal conductivity in air at elevated pressures in a negative temperature interval were not made in this work. Orig. art. has: 4 tables, 2 figures. I SUB CODE: 20/ SUBM DATE: 20Jul65/ ORIG REr: 007/ OTH REr; 005 Card 2/2 Apparatus for switching-in high pressure mercury discharge lamps with corrected chromaticity (RVDL). Svetotakhaika 3 no-3:16-19 Mr '57. (MLRA 100) 1. Moskovskiy elaktrolampovyy zavod. (Ilectric lighting, Mercury vapar) VASSIRMAN, A.L., insh. sman ignition devices for super high-pressure spherical mercury lamps. Svetotakhnika no.1:26-27 A 159. (MIRA 12: 1) * I.Moskovskiy elaktrolampovyy zavod. (Ilectric lighting, Mercury vapor) IVANOV, V.P.; VASS]MN, A.L.;-. BUKARIVA, A.A.; ZHWTSOV, V.P. Power supply for pulse Isaps operating under conditions of high repetition rates of flash. Usp.nouch.fot. 6:62-63 '59. 04IRA 13:6) (Photography, Flush light) (Blectric discharge lighting) s/196/62/000/020/008/021 E194/E155 AUTHORSi Marshak, I.S., Vasillyeva,V.I., and Vaaserman, A.1- TITLE: 'Sirius': the most powerful tubular xenon lamp in the world PERIODICAL: Referativnyy zhurnal, Elektrotekhnika i energetika. no.20, 1962, 6, abstract 20 V 31'. (Sveto.elkhnika, no.3, 1962, 7-.13). TEXTs The construction and characteristics of a 100 kW xenon lamp developed in the Moskovskiy elektr.-lampovyy zavod (Moscow Electric Lamp works) are fully described.. When operating with water-cooling, the luminous output of the lamp corresponds to a power per unit length of-1100 W/cm- reaching 50 lumens, per watt. The lamp operates without ballast and uses a starting device - similar to that previously developed for xenon lamps typcfs -AKCT-20000 WKST-20000). The lamps were tested in a special experimental rig set up in the engineering pavilion of the Exhibition of Achievements of the National Economy. This equipment consisted of three lamps of output up to 100 kW connected in the Cbtrd 1/2 'Sirius': the mbst powerful ... s/196/62/000/020/008/021 E194/E155 phases of a three-phase a.c. 380/220 V au'pply. The lamps were physically positioned in a star-pattern with mirror reflet;tors joined together in a unit mobile construction installed in the dome of the pavilion. The lighting is remote-controlled from a panel in a room of the pavilion. Cooling water for the lamps was pumped to the lighting fitting; to avoid overheating a water-pressure relay disconnected the lamps if the water pressure fell below 0.4 atm. The experimental equipment confirmed the possibility of using high-power ballastless xenon lamps with water cooling for illumination, 6 illuBtrations. 6 references. FAbstractor-s note: Complete translations Card 2/2 VASSERMAN, A.L., inzh.; ROSHCIII;':~., N.A., inzh. A differential current transfcr.-.er "or measurements in fluorencent lamp high-speed ignition networks. Svetotekhnika 8 no.10:25-27 0 162. OURA 15:9) 1, Moskovski-y elektrolampovyy zavod, (Flurorscent lighting) (Electric transformers) (Electric measurements) VASSERMAN, A.L., in3h. Starting device for large tubular DKST 201000 xenon-fillad lamps. Svetotekhnika 9 no.10-12 Ja 63. (KERA 16:1) 1. Moskovskiy elektrolampovyy zavod. (Fluorescent lamps) VASSMIAN, A.L.; SKVORTSOV, B.V, Elements of flaahtube feed systemn. Uap.nauchofoto 9:126-130 164o (MIRA 18:11) ACC NRt AT6001401 SOURCE CODE: UR/3180/64/009/000/0-159/0166 AUTHOR: Marsbak, L S.; Vasillyev, V.I.; VaBserman, A. L. ; Tokhadze, 1. L. ORG: none TITLE: Superpower ballastless tubular xenon lamps as a new ldnd of efficient sources r dr 41gh-,speed cinematography, ,,, ~: - -.- I SOURCE: p rn!t auchnoy ografil, Uspekhl n: fotografil, v. 9, 1964. Vysokoskotostnaya fotografiya I kinematograflya'(fligh-speed photog- raphy and cinematography), 159-166 TOPIC TAGS: light source, high spced photography, xenon lamp ABSTRACT: Following a brief outline of the historical development of xenon high-density dis- charge tubes the authors present a survey of theoretical and experimental data on superpower ballastless xenon lamps which may be used for high-speed cinematography. Scientific liter- ature and experiments carried out by the authors are used to discuss: 1) the dependence of the, specific resistance of tubular lampis on the electric gradient for various lamp parameters and cooling conditions; 2) light emission Intensity as a function of power per unit length of the discharge; 3) the voltage drop across lamps of different lengths for the same current; 4) char- acteristics of continuously operating xenon tubular lamps of different power; 5) the circuitry for igniting ballastless xenon a-c lamps; 6) a circuit diagram of devices for the switching of E xenon tubes into brief high-overload operating condition-, 7) the maximum powor liberated 12 L-15281-66 ACC NRt AT6001401 within the tube as a function of the length of operation under overload condiUom;; and 8) the spectral distribution of the radlation from tubular xenon Imnpa. The authors Uiank N, V. Rogatin, V. A. Suvorov, To M, Gory , L P. Orekhov V -B 'Milenin, and other comrades for their extensivepiFt-icip~tlon in this work. Orig. arko. has- 10 formulas, 7 figures, and 1 tab] SUB CODE: 14 / SUBM DATE: none / ORIG REF: 011 / OTH REF: 004 2/2 5(2) AUTHORS: Abrikosov, N. Kh., Vasserman, A. M.; SOV/20-123-2-19/50 b Poretskaya, L. V. TITLEs Investigation of the SnTe - GeTe System (Iseledovaniya sistemy SnTe - GeTe) PERIODICALs Doklady Akademii nauk SSSR, 1958, Vol 123, Nr 2, pp 279 281 (USSR) ABSTRACTs In pseudo-binary systems formed by semiconductor'compounds with a structure of the type NaCl, i.e. PbSe--PbTe and SnTe- PbTe, continuous solid sollations (Refs 1, 2) are formed. In the present paper a ternary syszem Sr--^Je-Te in the range between SnTe and GeTe was investigated. In both compounds the metal properties are stressed. The phase diagram of the system 3n-Te is known 'Refs 3 - 6). The only chemical compound SnTe in the system melts with an outspoken maximum at 790 0. No range of solid solutions on a Sn~e basis was found. Also in the system Ge-Te (Ref 10) there is only one com8ound Ge-Te which me..ts after a peritactic roaction at 725 . The limi if the range of solid solutions on the Ge-Te basis on the tellurium side is said to be located Card 1/3 (according to Ref 11) at the conc9ntration of 50 atom~4 Te. Investigation of the SnTe - GeTe System 3OV/20-1231-2-19/50 The phase diagram of the syatem Sn--Ge iB of the outectic type with a eutectic that is very close to that of pure tin. The melting temperature of.the eutectic is 232 0 (Ref 12). The authors malted the metals mentioned In the title in evacuated quartz ampules and mixed them by shaking; finally they were covIed in air. The alloys wert annealed at 320 0 for 320 hours (for the X-ray analysis at 5000). The results of the thermal analysi3 are given J-a figure 1. The liquidus- and solidus curves pass throuhh a minimum at a concentration of about 80% GeTe and at 700'. A;.! carves of the thermo- grams had a shape typical of the crystallization of solid solutions. The investigatica ;f the mi,)rcstructure of the alloys showed the formatior. o_~ 9. coritinuoas series of solid solutions. The X-ray analysis pravltd tAs results of either of the mentioned methodst the radiograms of annealed alloys showed a gradual transition of a face-centered cubic lattice of the compound SnTe to a face-centered rhombohedral lattice of GeTe. Table 1 gives the values of the constants of the crystal lattice of the alloys investigated. The above- mentioned investigation proved that in the system Sn-Ge-Te Card 2/3 in the range between the two nor.--isostructural compounds Investigation of the SnTe - GeTe System BOV120-123-2-191-,r, SnTe and GeTe a continuous series of solid solutions with a minimum in the melting-point diagram is formed. There are 4 figures, 1 table, and 12 references, 3 of which are Soviet, ASSOCIATIONt Institut metallurgii im. A. A. Baykova kkademii nauk SSSR (Institute of Metallurgy imeni A. A. Baykov of the Academy of Sciences, USSR) PRESENTEDs June 28, 1958, by 1. P. Bardin, Academician SUBMITTED: June 24, 1958 Card 3/3 CRJLI, V.Ye.p KOVRIQA, V.V.p VASSEM%N, A.M- Effect of Bupermolecular structures on the strength of polypropylene. Report to be presented at the 13th Conference on high-molecular compounds Moscow, 8-11 Oct 62 GULIJP V.Ye.; KDVRIGA, V.V.; VASSERW, I.M. Effect of Bupermolecular Btructure on the strength of po'2yprop7lene. Dokl, AN SSSR 146 no*3:656-658 3 162. (MIRA 15:10) la Moskovskiy inBtitut tonkoy khimichaskoy tekhnologii im. M.V.Lomonosova i Moskovskiy tekhnologicheskiy institut ayasnoy i molochnoy promyshiennosti. Fredstavleno akadem:Lkom. R.A.Karginym. (Propene) VASSjjq-V,jj , A. 1'4. ; Ill RO VT"-') EVA., V.. IXI doct,~isucl 1, De terminat i sn o,-;' cxyge n n .-e ta is and i nor - arn i c cc= crund z -.I- C- method of red-,~,--n.~ 4n ail :nert gas medium anal. khim. 19 no.11:1377-1384 164. ( 14 IFLA 16:2) 1. Vernadskiy Institute of Geochemistry and Analytical Chemistry, U.S.S.R. Academy of Sciences, Moscow. 7)1* the met'h-,j. '-cm. y 2-0 n, i . I L 354-' j 165. t i -48 IF, p I i " kb' u -i 'A anai"t cl7os*ycy k~3a a p ri, f~ W~il 1~5 il .1_Q 41 v je,G.; NETIMAN, M.B- VASSERMAN A 14 P' BUCii RO - '9, D1-4.qrf--butY1 r,;.troxidP- mf=~-. n to Ar Rd rrid I "' - kh -.T-3 qr Z~ur. struil. .46,,7-i.~8 My - .I# (~qRA 18:8) 1. Listitut khjmjchpz;koy fizlk', All SSSR- zh - YIIYIIS"l 0.11.1 inzh. t . A.Sh.p in -f G(MNKO~ 'V.1., imls., cooling ~cwers F-le"It 11 ta ;~ , P, -. 12 ) HodernizatiOn ct hnErbolic (VII 36 jjoj2t2'7--3o D 165. GAYEVOY, Ye.V., kand. sel'skokhoz. nauk;-ILA-~ inzhener- tekhnolog; U.P., stfirshiy In-hener; TRUDOLYUBOVA, P G.B., miadshily nauchnyy eot-idn'~k- G.A., rdad!3h!y nauchnyy sotrudnik; GEGUTZINA, 1.Yu.., mlladshiy nauchnyy sotrudnik; BLYAWAYA, N.V., tekhnik New method for the conservation. treatment of raw leather in a mobile apparatus. Trudy VNIIMP no-15:67-.78 163. (KI'R.A 17:5) .4 URSUL, M.M.j RADUL, M.M., red.; VA�9~~FJW, B.I., red.; POSAIZEENNIKOVA, Ye.F.J. red.; POLONSKIY, S.A.., tekfir~._red. [The canning industryof %& Moldavian S.S.R.; ways-of the development and distribution of the canning industry and its raw material base] Konservnaia promyshlennost MoldavBkoi SSR; puti razvitiia i razmashcheniia konservnoi promyshlennosti i ee syrIevoi bazy. Pod red. M.M.Radula. Kishinev, lzd-vo "Shtiinteam Akad. nauk Moldavskoi SSR, 1962. 181 p. (HIRA 16:5) 1. Chlon-korrespondent Akademii nauk Moldavskoy SSR (for Radul). (Moldavia-Canning industry) KISKIN, Petr Khristoforovich; VASSERMANO B.I., red.; LEDVICH, M.M., takhn. red. (Key for determining grape rootstock]Kliuch dlia oprodeleniia podvoev vinograda. Kiehinev, Izd-vo "Shtiiatea" Akad, nauk Moldavokoi SSR, 1961. 91 p. (MIRA 16:2) (Moldavia-Grapen-Varieties) BOROTNIKOV~ V.B;; VA red.; MARKOVICH, G.L., tekhri. red. [Problems of construction economics; based on the materials of the construction industry of the Moldavian S.S.R.] Voprosy ekonomiki atroitel'stva; po materialam stroitellnoi industrii MSSR. Kishinev, Izd-vo "Shtiintsall Moldavskogo filiala Akad. nauk SSSR, 1961. 185 p. OURA 14: 11) (Moldavia-Construction industry) I 'F , , , I : , * f ~ ! , ~ I ~, : 17 : ~. 1, i , ! I . " ~ 1 -, . %T, J. I . . - I I . . . r ",V 1 Y recent. data or. cf 'a upper Peci:()'. (VT 1-1 1. 1 1 ~ VASSEMAN, D.Ya.; .5iZONOV, N-V- Subdo, If the soutYern Timan aryd, t~e Volga- Parall.r.-IinV -- manik depoEits Ural replon. DoH. AN S",q l4r no.2:427-429 S '61. (MINA 14:9) 1. Predstavleno akademik,)m D.V-R3110inYm- (Timan Ridge-Geolory, Stratigraphic) (Volga-Ural reFion-Geoloas Stratigraph1c) A110SIMIt V.A.; VASSERMAII, B. Ya.; SAURICIV, N.V. New data on tl~e oil and gas potentials of caroonate sediments In the southm part of the Timan-Pechora area. Neftegazp geole I goof iz. no.41394,2 t6-) WRA 1787) 1. Voyvozbneftegazrazvedka. VASSERIMIN, 13.Ya.,' MODMINSKIY, M.Sh. Relation of the oil potential of the part of the Pechora depreasion to the Neftegaz. geol. i geofiz. no.9:15-20 str-,;cV;res In t'-- scr~.thern time of their forzation. 164. (MM 17:11) 1. Treat Voyvozhneftegazrazvedka. VASSFJMN,l B._Y.a.; LITVIIIENKO, N.I. Geoiogical structure and oil occ-arrences of the Pashnya oil field. Jiuftegaz. gool. i geofiz. no.11:3-6 165. (MIRA 18:12) 1. Trest "Voyvozhneftegazrazvedka" i Ukhtinskoye territoriallnoye geologicheskoye upravleniye. Kha4s) A.Yao; VASSEYNAN, D.Ya. Certain features of the zLru~~tur,: and distribution of oil fields in the Pechora depression and main trends of their further search. Oeol,nefti i gaza 9 no.21l5-20 F 165. (MIRA 18:41 1. Ukhtinakoyo tarriLorialIncya geologicheskoye upravieniye.