SCIENTIFIC ABSTRACT TOLSTOPYATOVA, A.A. - TOLSTOUSOVA, Z.A.

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SCIENTIFIC ABSTRACT
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TOLSTO-PYATOVA,, A.A.j yUy TSI-TgyUANo [Yu Chli-chluan]; DULITSKAYA, K.A. Catalytic propertieo of neodymium oxide in the reactions of debydrogenation of-tetral-in. Izv. AN SSSR. Ser. khim. no.12: 2095-2100 D 163. (MIRA 17:1) 1. Institut organicheskoy khimii im. N.D. Zelinskogo AN SSSR. KONENKO, I.R.; TOLSTOPYATOVA, A.A.; BALANDIN, A.A. Scandium oxide as a catalyst of dehydrogenation and dehydration. Izv. All SSSR. Ser. khim. no.11:1899-1905 11 163. (MIRA 17:1) 1. Institut organicheskoy khimii imeni N.D. Zelinskogo AN SSSR. ) A. A.; TOISTOPYATOVA, A. A. "Selectivity of catalysis and bond energies." report submitted to 3rd Intl Cong on Catalysis) Amsterdam.. 20-25 Jul 64- Inst, or Organic Chemistry im Zelinskiy., AS USSR, Moscow. - TOLSTOPYATOVA, A.A.,- BALANDIN, A.A.; YUY TSI-TSYUAN' [Y~ Chli-chl~an) Kinetics of dehydrogenation and dehydration of isopropyl alcohol and of the dehydrogenation of tetralin on lanthanum oxide. Zhur.fiz.khim. 37 no.lOt2220-2227 0 163. (MIRA 1722) 1. Institut organichaskoy khimii AN SSSR. BALANDIN, A.A.; KONENKO, I.R.j_ TQ1SJ-QMTO~A,_A-.A. Kinetics of dehydrogenation and dehydration of ethyl and isopropyl alcohols on ytt4Lum oxide, Kin.i kat, 2 no,6:90Q-906 N-D 161. - (MIRA 14:12) 1. Institut organicheskoy khimii imeni N.D. Zelinskogo AN SSSR. (Ethyl alcohol) (Isopropyl alcohol) ~(Dehydrogenation) (Dehydration (Chemistry)) BAIANDIN, A*A*, akademik; TOLSTOPYATOVA. A NAUMV, V.A. Bond energies of interaction between organogens and the surface of oxide catalysts. Dokl.AN SSM 148 no.42825-828 F 163. WMA 16:4) 1. Moskovskiy goErudarstvennyy universitet im. M.V.Lomonosova. (Chemical bonAs) (Chemical elements) (Catalysts) FERAPONTOV, V.A.; BAIANDINq A.A.; TOLSMPYATOVA, A.A. Catalytic dehydrogenation of ethylbenzene th styrene on cadmium oxide in the presence of water vapors. Izv.AN SSSR.Otd. khim.nauk no.3s4l4-423 Mr 163. (KIRA 1634) 1. Institut organicheakoy khimii im. N.D.Zelinskogo AN SSSR. (Benzene) (Styrene) TOISTOPY a A ; BALANDIN, A.A.; NAUMOV, V.A. Kinetic method used in the determination of bond energies of the reacting atoms of organic molecules having a blue moIrWenum oxide surface. Izv.AN SSSR.Otd.khim.nauk no.3&423-429 Hr I _1-_ (MIRA 16:4) 1. Moskovskiy gosudarstvennyy universitet im. M.V.Lomonosova. (Chemical bonds) (Molybdenum oxides) (Organic compounds) TOLSTOPYATOVA, A.A. BALANDIN., A.A.; FYN BI-SYAN [POOng Pi-4isiaag] Kinteics of the dehydrogenation and dehydration of isopropyl, alcohol and of the dehydrogenation of tetralin on thulium oxide. IZV.AN SSSR. Otd.khIm.nauk no.9:1524-1533 S J62. (IffRA 15:10) 1. Moskovskiy crosudarstvennyy universitet im. M.V.Lomonosova. (Isopropyl alcohol) (Dehydrogenation) (Dehydration (Chemistry)) (Naphthalene) BALANDIN, A.A.; TOLSTOPYATOVA,_A.A.; PYN BI-SYAN (PIOng Pi-holang) Catalytic properties of dysprosium oxide with respect to the reaction of &hydrogenation and dehydration of alcohols and debydrogenation of tetralin. Izv.AN SSSR.Otd.khim.nauk no.6: 974-980 '640 (KRA 15:'8) l.. Moskovskiy gosudarstvennyy universitet im. M.V.Lomonosova. (Dysprosium oxide) (Catalysis) (Dehydrogenation) TOLSTOPYATOVAJO A.A.; BALAVDIN, A.A. PYN BI-SYAN [P'8ng Pi-haiang] Kinetics of dehydrogenation and dehydration of isopropyl alcohol and dehydrogenation of tetralin of dysprosium oxide. Izv.AN SSSR~ Otd.khim.nauk no.7:1-154,-1163 J1 162. (MIRA 15-7) 1. Mbskovskiy gosudarstvennyy universitet im. 14.V.Lomonosova. (Chemical reaction, Rate of) (Catalysis) (Dysprosium oxide) . . . . . . . . .... 13W 531L P 1v TOLSTOPYATOVA$ A.A.;_ PYN BU-SYkN [Ptgng Pi-hsiang]; BALAIMIN, A.A. Kinetics of dehydrogenation and dehydration of isoprop,71 alcohol and of dehydrogenation of tetralin on ytterbium oxide. Izv.AII SSSR.Otd.khim.nauk no.8:1322-1329 Ag 162. (MIRA 15:8) 1. 14ookovskiy gosudarstvennyy universitet im. M.V.Lomonosova. (Isopropyl alcohol) (Naphthalene) (Dehydrogenation) BATA INJI A.A.; TOLSTOPTATOVA. A.A.; NAUMV, V.A. Determination of bond energies of the reacting atoms of organic molecules with the MC~ catalyst surface using a kinetic method. Izv,AII SSSR.Otd.khim,,.nauk no.70250-1154 Jl 162. (KRA 15:7) 1. Moskovskiy gosudarstvennyy universitet im. M.Moomonosova. (Chemical bonds) (Mlybdenum oxide) (Chemical reaction., Rate of) BALAMD1, A.A.; MI BI-SYAN [PIOng Pi-hsiang); TOLST-OPYATOVA, A.A. Kinetics of dehydrogenation and dehydration of IsopropjvI alcohol and of dehydrogenation of tetralin on gadolini= oxide. ImAll SSSR.Otd.khim.nauk no.8.-1330-1336 Ag 162, (MIRA 15:8) 1. Mookovskiy gosudaretvennyy universitet im. M.Lomonosova. (Isopropyl alcohol) (Hapththalens) (Dehydrogenation) TOISTOPYATOVA, A.A.; ULAWIN, A.A.; MATYLIBBENKO, V.Kh. Determination of bond energies of atoms of organic molecules reacting with the a-prface of the YhO catalyst. Izv.AN &9SR Otd. khim.nauk no.8d333-3.336 Ag 160. (MIRA 15:5) 1. Moskovskiy gosudarstyennn universitet In. MoVAomonosova i Lwtitut organicheskoy kbildi im. N.D.Zelinskogo AN SSSR. (Chemical bonds) (Chemical reaction, Rate of) S/06 62/000/008/002/016 B1 01 YB1 80 AUTHORS: Tolstopyatova, A. A., Ping Pi-hsiang, and Balandin, A. A. TITLE: Kinetics of the dehydrogenation and dehydration of isopropanol and the dehydration of tetralin on ytterbium oxide PERIODICAL: Akademiya nauk SSSR. Izvestiya. -Otdeleniye khimicheskikh nauk, no. 8., 1962, 1322-1329 Ta-T: Data was obtained on the catalytic dehydration of i-propanol and the dehydrogenation of i-propanol and tetralin on Yb 203' using methods described earlier (Dokl. AN SSSR, 138, 1365 (1961); Izv. ml SSSR, Otd. khim. n., 1962, 974, 1154). The low specific surface area of the catalyst (9.1 M2/g) precluded capillary condensation and complications due to diffusion. 'When the catalyst was mixed with quartz powder in a 1:1 ratio, the reaction took place isothermally. z, the relative adsorption coeffi- cient of the reaction products (H 2 0, C3H31 acetone's H2, naphthalene), and the thermodynamic functions AH (kcal/molo)p AP (kcal/mole), AS Card 1/3 S/062/62/000/008/002/016 Kinetics of the dehydrogenation ... B1011BI80 (kcal/mole-deg) were calculated: dehydration of i-propanol dehydrogen ation of i-propanol 0C z &H tLF AS 0C z AH AF AS H2 0 aoet 325 7.23 -18.7 -2-39 -10-4 345 2-56 -21.9 -Ie13 -33-5 365 3-48 -1-57 -10-3 365 1-54 is -0-54 zC3H6 zR2 329 1.60 -23 .6 -0.69 -38-3 325 0-15 34.7 2.24 54-4 36o o.61 It 0-4b Is 345 0.40 of 1.13 54-5 dehydrogenation of tetralin z napht' 21 R2 500 1-37 26-5 -0-49 34-9 500 1-40 -48-4 -0-49 -62.0 524-5 2.32 It -1-35 530 0-42 11 1-39 -62.1 The real and apparent activation energies and the energy of adsorption of the C,11 and 0 atoms onto the sur faoe of the Yb 20 3were calculated from the Card 2/3 S/06 62/000/008/002/016 Xinetics of the dehydrogenation B101 Y2180 above data (the first figure being the apparent value, the second the true value, in kcal/mole): dehydration of i-propanol E H20 25-19 30.-6; dehydrogenation of i-Propanol E 20.6, 22.9; dehydrogenation of tetralin H2 6A2 34-7, 36.6; QC-cat 22.1, 19.4; QH-cat 53.5; 55.1; QO-cat-52-5, 49-7. There are 3 figures and 13 tables. ASSOCIATION: 'Moskovskiy gosudarstvennyy univeraitet im. M. V. LomonosovA (Moscow State University imeni 11. V. Lomonosov) SUBMITTED: February 13, 1962 Card 3/3 TOLSTOPYATOVA, A.A.; KONENKO, I.R.; BALANDDI, A.A. Bond energies of carbon, hydrogen, and oxygen atoris of organic molecules with yttrium oxide. Kin.i kat. 3 no.1:103-106 '62. (MIRA 15:3) 1. Institut organicheskoy khimii imeni N-D.Zelinskogo AN SSSR. (Chemical bonds) (Yttrium oxede) (Catalysis) (Organic compounds) IA '13 A:-- ' OR m a -MMY-05 +'03 'jjO --- 5"' Ahad. Ndqh ;r9) ~dohcO % C%j -3L- ~y zi-cito 41~11 '0 -348 ve catal lip t297 7vT 'ctivity of Z,Os 38 1 with theorye Y. )". itr.~~yd "S llar fur all It , ti i -lu- ire 1%1'. nbladin -!rgd-~: "6 very the =ti,, "I" -, " , I diffo, Z6fij~Aorably,', fr6,11 tjlc but t1le '111'a j calc:ulatc talysts, %v Ul't ge cataly3t_o with thc cataly5t' 1 14i ond CrOscLL it. TRusc . cl", to thr"S'3 found I'll is uch jo%ver. :bond-Olergy BALANDIN, A.A.; T~I~~TOYAJQ-VA-~,-A~.A.; DUD~IK, t. Catalytic properties of thorium dioxide in the dehydrogenation and dehydration of alobhols, and in the dehydrogenation of cyclic hydrocarbons. Kin.i kat. 2 no.2:273-284 Mr-Ap 161. RIA 14.6) 1. Moskovskiy gosudarstvennyy universitet, kafedra organicheskogo kataliza. (Thorium oxide) (Dehydrogenation) (Dehydration (Chemistry) TOLSTOPYATOVA, AI~A.; BALANDIN, A.A., akademik Regularities in the catalytic properties of rare earthae Dokl*PII S,VR 138 no.6:1365--d368 Je 161- (MM 14:6) I 1. Institut organicheskoy khi-ii im. N.D.Zelinskogo AN SSSR i Moskovskiy gosudarstvemyy universitet im. M.V.Lomonosova. (Rare earths) (Catalysis) BALANDIN, A.A.; STSHIZHEVSKIY, V.; TOLSTOPYATOVAj, A.A. Thermal effect of the reaction of alcohol dehydration affecting the results of kinetic measurements. Vest.Mosk. un. Ser.2:lddm. 17 no.1:3'0-33 Ja-F '62. (MIRA 15:1) 1. Moskovskiy gosudarstvennyy univers~'Set, kafedra organicheskogo kata.liza. (Alcohols) (Heat of dener7ation) (Catal7sis) �r i Mil BALANDIN) A.A.;,TOISTOPYATOVA, A.A.; DUDZIK, Z. Catalytic properties of thorium dioxide in the dehydrogenations and dehydration of aicbhols., and in the dehydrogenation of cyclic hy- drocarbons. Kin.i kat. 2 no.2:273-284 Mr-Ap 161. (14-TRA 14:6) 1. Moskovskiy gosudartsvennyy universitet, kafedra organicheskogo kataliza. (Thorium oxide) (Dehydrogenation) (Dehydration (Chemistry)) TOLSTOPYATOVA, A.~.) BALANDIN, A.A.; MATYUSHENKO, V.Kh.; PETROV, Yu.1 Kinetics of the dehydrogenation and dehydration of alcohols-, and of the dehydrogenation of hydrocarbons over WS2 and MoS2 catalysts. Izv. AN SSSR Otd.khim.nauk no-4.-583-590 AP 161. (MM 34:./+) lo Inatitut organicheskoy kbimli im. N.D.Zeiinskogo AN SSSR. (Dehydrogenation) (Dehydration (Chemistry)) (Molybdenum sulfide) (Tungsten sulfide) TOLSTOPYATOVA A.A.; KONEK09 I.R.; BALANDINg A.A. Catalytic properties of yttrium oxide.-Conversions of alcohols and hydrocarbons. Kin. i kat. 2 no.1:131" 143 Ja-F 161. (Mmk 14:3) 1, Institut organichaskoy khimii imeni N.D. Zelinakogo AN SSSR. (Yttrium oxide) (Alcohols) (Hydrocarbons) BAJ~MII, A..A.-,--TOLSTOPYATOVA, A-A; KONMO, I-R. Study of the catalytic converalons of isoprojq1 alcohol and cyclic hydrocarbons on titanium dioxide (anstase) by means of a differential thermocouple. Izv. AN SSSR.Otd. khim. nauk no.l2s2096-2102 D 160. (MM 13:12) 1. Institut organicheskoy khImR Im.N.D.Zelinskogo AN MR. Ueopropyl alcohol) (Eydrocarbons) (Anataae) TOLSTOFnYhT!0TV~Aj_~A.; KOMMKO, I.R.; BALAIMIN., A.A. Kinet-ics of dehydrogenation and dehydration of isoprop - I Y1 alcohol over titanium dio-dde (Anatase). izv. AIT SSSR. Otd. khim. nauk no. 1:38-44 Ja t6l. (MRUt Ili: 2) 1. Institut organicheskoy khimii im. I.I.D. Zelinskogo AIT SS311. (Anatase) (Isopropjl alcohol) KOILE,110, I.*~.; TOLIjTCI"- R-W., A.!.. F,ffect of the proT.4rz..tior matl,r)d on the catc-lytic prol,,erties of titan~lm dioxide in ri~:Lc-'Loiom, of ethyl ~;,nd --*sor;-.cpll alcohol and &yplohe::ane. Izv. '2T, SSS-?.. Otd. Ichim. nauk no, 1:/+5-50 Ja 161. EUMi. 14 ; 2 1. Imtl"'.Ut or-i nichl-zlzoy Idiixdi 'elinslcogo A.". 6340'lc- cj (Titanim oxide) (ZthlAnol) (Isopropyl alcohols) (Cyclohe;cane) J TOLSTOPYATOVAt A.A.; BALANDINp A.A.; KONMO, I.R. Energies of the bonds between reacting organic compounds and the cataly-tic active centers~of titanium'dioxide. Izy. AN SSSR. Otd. khim. nauk no.2:214-.217 F 161. (MIRA 14:2) 1. Institut organicheskoy khimii im.N.D.Zelinskogo AN SSSR. (Titanium oxide) (Chemical bonds) S10621611000100110041016 B101/B220 AUTHORS: Tolstopyatova, A. A., Konenko, I. R., and Balandin, A. A. \j TITLE: Kinetics of dehydrogenation and dehydration of isopropyl alcohol on titanium dioxide (anatase) PERIODICAL: Izvestiya Akademii nauk SSSR. Otdeleniye khimicheskikh nauk, no. 1, 1961, 38-44 TEXT: By way of introduction the authors offer a s' urvey of reports dealing with the catalytic efficacy of T102, and then report on the dehydrogenation and dehydration of isopropyl alcohol on anatase. Regarding the production of the catalyst they refer to another report published by them. For the verification of the kinetics of monomolecular hetero eneous-catalytio reactions they 3roceed from the equation k - A 7z Z )lnA,/'Al 1)m (1 . A is the volume of alcohol 1 2- 3 % -M)-(Z2+Z3- I converted per minute, which is introduced at the rate v; m is the volume of are the relative propylene (or hydrogen) formed per minute; Z2, Z3( adeor.ption coefficients of the reaction products hydrogen and acetone Card 1/3 B10621611000100110041016 Kinetics of dehydrogenation and dehydration... B101/B220 in the case of dehydrogenation; propylene and water in the case of dehydration)l Z2 and Z3 were calculated from Z - (mo/m-l)/(100/p-1) (2), where mo, m are the amounts of the reaction products resulting on the passage of pure alcohol (m0) and on the passage of a p molar mixture with the reaction product. Since Z is the equilibrium constant of the displacement of the isopropyl alcohol from the catalytic centers by the reaction products, it was possible to calculate also 6F of the free energy, AS of entropy, and AR of the heat content. The adsorption coefficient Zac of acetone was found to be highly dependent on temperature and much less so on the degree to which the catalyst was covered with carbon. The following is indicated for not carbonized T102: Zac = 2.4 at 282OC; 1.7 at 2940C; 1.2 at 3100C. For carbonized T102 these values amounted to 2.7, 1.8 and 0.9. The adsorption coefficient ZH2 of the hydrogen remains constantly 0.9 in the range of 276-3060C. Moreover, it was found that ZH20 - 1.9 at 2820C, 1.4 at 2940C, and 0.9 at 3100C, whereas Zpropylene remains a constant 0.2 in the temperature range of 300-3300C. A. M. Rubinshteyn and S. G. Kulikov are mentioned. Card 2/3 S1062161100010011004-1016 Kinetics of dehydrogenation and dehydration ... B101/B220 There are 1 figure, 8 tables, and 24.references: 8 Soviet-bloc and 13 non-Soviet-bloo. ASSOCIATION: Institut organicheskoy khimii. im. N. D. Zelinskogo Akademii nauk SSSR (Institute of Organic Chemistry imeni N. D. Zelinskiy, Academy of Sciences USSR) SUBMITTED: June 29, 1959 ~ I Card 3/3 5106 61/000/001/005/016 B101XB220 AUTHORS: Balandin, A. A., Konenko, I. R., and _Tolstopyatova, A. A. TITLE. Effect of the method of production on the catalytic proper- ties of titanium dioxide in the reaction with ethyl alcohol, isopropyl alcohol, and cyclohexane PERIODICAL: Izvestiya Akademii nauk SSSR. Otdeleniye khimicheskikh nauk, no. 1, 1961, 45-50 TEXT: The authors were concerned with the investigation of the catalytic properties of titanium dioxide. Here, they studied the dependence of those properties on the method of TiO 2 synthesis. Four specimens were used. Catalyst 1 (anatase), whose production is described in Ref. 1, a previous report of the authors; catalyst 2, obtained by hydrolysis of TiCl 4 by means of qmmonia solution in a weakly acid medium at room temperature; catalyst 3, obtained by precipitation of Ti(OH)3 from TiCl3 by means of ammonia at room temperature and conversion to Ti(OH) 4 which occurred automatically Urd 1/5 Effect of the method of production.... S/062/61/000/001/005/016 BIOI/B220 while washing the precipitate; catalyst 4, obtained by hAmlysis cf ethyl ortho- titanate by means of distilled water at room temperature. The further treatment of the hydroxides for the purpose of obtaining TiO2 was per- formed according to Ref. 1. Ethanol reacted with these catal t accord- ing to three reactions: a) dehydrogenation, b) dehydration, c~shydrogena- tion of the resulting ethylene. Moreover, up to 2% ethyl acetate was formed on all four catalysts. The reaction of isopropanol corresponded to data mentioned in Ref. 1. Due to the growing accumulation of carbon on the catalyst, the rate of dehydration increases, whereas that of de- hydrogenation decfeases. Cyclohexane is dehydrogenated on all four catalysts. The differences between the catalysts regarding the activation energy E and the factor k0 of the Arrhenius equation are listed in Table 8. The linear function log ko = a6 + b (a, b - constants) is conserved for all reactions. A. M. Rubinshteyn and S. G. Kulikov are mentioned. There are 2 figures, 8 tables, and 6 referencest 4 Soviet-bloc and 2 non-Soviet- bloc. Card 2/5 Effect of the method of~ product-i-on... 3/062/61/000/001/0~5/016 BIOI/B220 BallISHIle cnocoft OpIlrelosileiXX ZMAKMTOP& 7102 "a BM-IRXW OfftPrItA aJLTHUZINK 14 Ic tlajut wop tit KQrAfilf- 2 3 .2 4. 0. jjlerHAporeH"3swiR qvzowm cnmpT& 22.8 20 4 0,4 12,4 t0$ t0 1,9-101 1,4 4. Q, JAMIAPMWIS sninosoro enmpts 250 25:4 0,0 12,5 : 1:5 tOf 5,6406 V in. 0. UerHAPaT8WfO m3onponmowro cnifpTa 22 9 9,1 20,2 2 17 3 7,104 9.1-105 1,0 i it. o. forilAporettitnwin svifietfa 21 2 24,2 MO 10:8 1: 8 - 10') 1,0- tOl 1.3 4 q- 0- l0lerHAPOreHH30OR wtuore=H& 19:0 14,7 2i,G 15,0 8,7406 5,1.104 1,3 ~ q. 0. (XAerllAporeHH3aLwsi smoripawowro CnHpTa 9,1 10,4 1.01104 2,2.104 yq. 0. qaertIAPSTURR mapommowro cnupTa 24,4 15,3 4,5.109 6,9-t0$ H. o. flAerHAporemnatinn tisonponHao3oro cnupu 1,9.101 - 11. 0~ tJlerHAporeHH38WIR ttworexcamt 25 2 4,9.101 - - q.L 0. Aerl]AporemHugusi nponmosoro cups 19:4 2 3.100 - it q. 0. (yAentApATaww H.nponunowm cnHpTs 12,1 4 5. 1(~ - Card 4/5. COMSMIte -101 -101 40111 -104 - - - - R 3 4 1,2-104 4,4404 2,8407 2,7406 i0# 3,5406 KHTO.AH3JTOP Effect of the method of S/0621611000100110051016 4 2 3 B101/B220 .2,94 281 3,0t 3 05 2,73 2.90 2,70 2:70 .2 39 2 28 2,54 2 31 :0 3,01 3' 2:91 3 1 110 3,20 3,12 3.53 3,3,0 24 2,40 - 2:53 2,02 - 2,25 3,27 2 71 3:05 2,73 2,96 2,89 2,60 Legend to Table 8: Effect of tNe method of preparing the TO catalyst Oil 2 the amounts of activation energies. 1) Condition of catalyst surface; 2~ reaction; 3) catalyst; 4).partially carbonized; 5) completely carbonized; 6.1 not carbonized; 7) dehydrogenation of ethanol; 8) dehydrbLtion of ethanol; 9) dehydration of isopropanol; 10) hydrogenation of ethylene; 11) dehydro-1- genation of cyclohexane; 12) dehydrogenation-of isopropanol; 13) dehydro- genation of propanol; 14) dehydration of n-propanol. Card 5/5 TOIZTOPYATOVA, A.A. A.A.Ralandin's work in the field ef haterageneous catal7sis. Vout.Kbak.un.Sor.=Lt,, makho, astron., fiz., kh1u. 14 no.): 159-169 '59. (mm 13:5) (Catalysis) (Balandin, Alakeei Alakcandrovich, 1898) 81725 20 S/O 0 133/01/36/070 BO11 B003 AUTHORS: Tole ouatom A. A., Balandin, A. A.9 Academician, Konenico, - . .- -- TITLE: Catalytic Transformations of Alcohols and Cyclic Hydro- carbonslon Titanium Dioxide PERIODICAL: Doklady Akademii nauk SSSR, 1960, Vol. 133, No-19 pp. 130 - 133 TEXT: Although titanium dioxide is easily available, it belongs to the little investigated catalyst lThe authors wanted to study its cata- lytic properties with various modes of preparation, in reactions with ethyl-9 isopropyl, and n-propyl alcohol as well as with cyclohexane, cyclohexene, and 194-cyclohexadiene. Moreover, they wanted to investi- gate the.kinetics of these reactions and the energies of the bonds of C-,7 H-,, and O-atoms with the TiO2surface. The method of the differen- tial thermocouple is used for the study of the catalytic reactions. Fig. 1 shows the position of the catalyst in relation to the thermo- couple. The electromotive force (emf) was uninterruptedly recorded on Card 1/3 81725 Catalytic Transformations of Alcohols and S/02q&/133/01/36/070 Cyclic Hydrocarbons on Titanium Dioxide BOIV~003 a potentiometer of the typ! 0 _?2P-OL(EPP-09)- Apparatus and methods are described in Ref, 4. By combining the above method with analytical meth- ods the authors found that in isopropyl alco,hollthe surface of the cata- lyst is coated by carbon-containing sediments. In this wayp the rela- tion between dehydrogenation and dehydration of the alcohol is consider- ably influenced. Within the first 2 - 5 min it is only dehydrogenated. Subsequentlyq the two processes mentioned take place, and after 20-25 min there occurs dehydration only. Meanwhileg the total amount of the gas liberated per unit of time remains unchanged. All this proves that the centers that are active for dehydrogenation, are poisoned after decarbonization with respect to this reaction, but at the same time are capable of dehydrating the alcohol at the same rate (Table 1). Also the regeneration conditions of the catalyst were determined with the same apparatus: The carbon film was removed after each experiment by means of a strong air ourreato with the catalyst being previously brought to a temperature exceeding the one of the experiment by 40-50 C. Regeneration usually took 20-30 min, The authors studied the influence of the mode of preparation of T102 on the catalytic properties on four samples: No. I - by precipitation of the hydroxide from TiCl 4 with Card 2/3 81725 Catalytic Transformations of Alcohols and S102016011331011361070 Cyclic Hydrocarbons on Titanium Dioxide BOIIIB003 water, No. 2 - the same with ammonia. No. 3 by oxidation of freshly pre- pared Ti(OH)3 (precipitated from T'Cl3 with ammonia) with air, and No. 4 by hydrolysis of orthoethyl titanate. it was established by X-ray strue- taral analysis that anatase resulted in No. 1. Table 2 shows the reac- tions studied in certain temperature ranges, the activation energies 'C as well as Ko of the Arrhenius equationj furthermoreq the degree of de- carbonization of each sample surface. It may be seen from these data and Table 4 that the mode of preparation exerts a great influence on the above-mentioned values and the binding energy. Table 3 shows the depen- deRce of the adsorption coefficient z on AHO (heat content) the entro- py ASoq and the change in free energyAFO. The binding ener6 values were oaloulated for the first time (Table 4). There are I figure, 4 tableap and 11 references: 10 Soviet. ASSOCIATION: Institut organicheakoy khimii im. N. D. Zelinskogo Akademii nauk SSSR (institute of Organic Chemistry imeni N. D. Zelinskiy of the Academy of Sciences,_USS SUMTTED: April 29 1960 Card 3/3 UU-JUJ S/195/60/001/004/008/015 .54--5oo B017/BO55 AUTHORS: Tolstopyatova, A. A., Balandin, A. A., Stshizhevskiy, V. TITLE: The Kinetics of Alcohol Deh:.!dration on Tungsten Oxide and the Energy of Carbon, Hydrogen, and Oxygen Bonds With Catalysts PERIODICAL: Kinetika i kataliz, 1960, Vol. 1, No'- 49 PP- 558-565 TEXT: The kinetics of the dehydration of ethyl, isopropylt n-butyl and tart-butyl alcohol and cycloh6xanol on W 205 were investigated under isothermal conditions. This catalyst was also used to study the de- hydrogenation of methyl alcohol and 1,2,3,4-tetrahydro naphthalene.-The catalyst was prepared by subjecting the yellow tungsten oxide WO 3 to heat treatment in air at 350-4g0 0C for 5-6h, and subsequent treatment with alcohol vapors at 200-390 C. Thermal effects in dehydration reactions of n-butyl alcohol are shown in Table 1. Table 2 gives the apparent activa- tion energies of alcohol dehydration on the tungsten-oxide catalyst. A relation was found to exist between the apparent activation energy and Card 1/4 88360 The Kinetics of Alcohol Dehydration on Tungsten S/195/60/001/004/008/015 Oxide and the Energy of Carbon, Hydrogen, and B017/BO55 Oxygen Bonds With Catalysts the structure of the alcohol. For ethyl and n-butyl alcohd~ the apparent activation energy of dehydration is 30 kcal/mole, for isopropyl alcohol, 24 kcal/mole and for tert-butyl alcohol, 18 kcal/mole. The true activation energies of alcohol dehydration (isopropyl and butyl alcohols) were determined at 26.1 kcal/mole for isopropyl alcohol and 33.4 kcal/mole for n-butyl alcohol by means of the kinetic equation by Balandin (Ref. 20). The relative adsorption coefficients of the dehydration products from n;C,H6OH and iso-C,H OH as a function of temperature are given in T b e 3. From this il may be seen that the relative adsorption coefficients are independent of temperature. Results obtained in the kinetic determination of the dehydration of n-butyl and isopropyl alcohol are shown in Table 5. The true activation energy is 3 kcal/mole higher than the apparent activation energy. The alcohols to be dehydrated are oriented with their functional groups towards the surface of the catalyst: C - C'~ H 0- The kinetic method was used to determine the energies of the bonds of the Card 2/4 I The Kinetti--s of _lcohol Dehydration on Tungsten S/195/'0/001/004/008/015 Oxide and the Energy of Carbon, Hydrogen, and B017/BO55 Oxygen Bonds With Catalysts carbon, hydrogen, and oxygen atoms with the active centers of the W 205 surface. The bond energies were found to be a function of the structure of the alcohol. The energies of the bonds of reacting atoms and molecules with the surface of the W 205 catalyst are given in Table 6. Table 6 Activation Bond Energies Alcohol Energy of '~H-Cat qc-cat %-Cat Dehydration n-Butyl 29.9 56.7 24.1 39.4 Ethyl 29.4 56.4 24.5 39.7 Isopropy! 23.7 52.6 27.6 43.5 Cyclohexanol 21.9 51-5 29.5 44.6 Tert-butyl 17.8 48.7 32~2 47.5 I. Ye. Adadurov and P. Ya. Krayniy are mentioned. There are 6 tables and 25 references: 24 Soviet and 1 German. Card 3/4 83360 The Kinetics of Alcohol Dehydration on Tungsten S/195/. 60/001/004/008/015 Oxide and the Energy of Carbon, Hydrogen, and B017/ 055 Oxygen Bonds With Catalysts ASSOCIATION: Moskovskiy gosudaretvennyy univerait~.-.t (Moscow state University) SUBMITTED: May 13, 1960 Card 4/4 TOLSTOPYATOVA, A.A.; BAIANDIN,A.A. ; STSHIZHEVSKIY, V. Kinetics of dehydration of alcohols on tungsten oxide, and energies of the bonds between the catalyst and carbon, b~*&rogea, and oxygen. Kin. I kat. 1 no. 4:55B-565 N-D 160. kMIRA 13:12) 1. Mookovskiy goeudaretvannyy universitet (Dehydration (Chemistry)) (tungsten oxide) (Chemical bonds) ---- ---------- s/o62/6o/ooo/oo8/1o14/f03,3/XX B013/BO55 AUTHORS: _T Balandin, A. A., and Matyushenko, _qjg~tq,Uatova, A. A., V. Kh. TITLE: Determination of the Bonding Energies of the Atoms of Organic Molecules Reacting With the MnO Catalyst Surface PERIODICAL: Izvestiya Akademii nauk SSSR. Otdeleniye khimicheskikh nauk, 1960,,No. 8, pp. 1333-1336 TEXT: The present paper is a continuation of the investigation into the transformation of alcohols on manganous oxide begun in Refs. 1 and 2. The experimental methods and catalyst 1)roparation have been deaoribed previous- 0 0 ly (Ref. 2). Dehydration was carried out between 330 and 380 C. The gaseous products consisted of unsaturated hydrocarbons only. The first series of experiments was performed to determine the apparent activation energy (Table 1, Fig. 1). The siativatton ontirgy calculated by manna of tho Arrhenius equation from the relation log ni - f(I/T) was 24.1 kcal/mol. Relative adsorption coefficients of isobutylene (Table 2) and'water (Table 3) were determined. The determination of the relative adsorption coeffi- Card 1/3 Determination of the Bonding Energies of the S106216010001008101410331XX Atoms of Organic Molecules Reacting With the B013/BO55 MnO Catalyst Surface cients and their temperature dependence permitted calculation by the method described in Ref. 5 of the changes in free energy, enthalpy and entropy produced by displacement of trimethylcarbinol from the active cent'ers of the cs,talyst by isobutylene and water (Table 4). The true activation energy for the dehydration of trimethylearbinol, calculated fr~om the relation log k = f(11T) (F_ = 31.0 kcal/mol) was found to be kcal higher than the apparent activation energy ~E' = 24.1 kcal/mol). the strength o~ this investigation, the authors were able to determine 6.9 On the bonding energies of the atoms reacting with the catalyst surface according to the well-known method (Ref. 6). These reactions are: C-C C-0 C_f I I I I I H H 11 11 0 (I) debydrogenation of hydrocarbons; (II) dehydrogenation of alcohols; (III) dehydration of alcohols. The following bonding energies were found: ~H-k - 50-75, QC-k = 26-7 and QO-k = 36.8. V. N. Kondratlyev is mentioned. Card 2/3 Determination of the B,,,ndirjq Enert,n;ius cf tiie S/o62/60/000/008/014/033/XX Atoms of Organic Molecules Reacting With the B013/BO55 MnO Catalyst Surface There are 1 figure, 4 tables, and 8 Soviet references. ASSOCIATION: Moskovokiy gooudlarstvennyy universitet im. M. V. Lomonosova (Moscow State Univergity.imeni M. V.. Lom.o.nosov). Insti-t~v,o-rgalliclle-s,k-o-y--khimii im. N. D. Zelinskogo Akademii nauk SSSR 'Inatitute of Drt~anic Chemistry imeni N. D. Zelinskly of the Academy of Sciences USbR) SUBMITTED: January 14, 1959 Card 3/3 s/o8i/60/0Q0/621/Oo5/bl8 AOO5/AOO1 Translation from: Referativnyy zhurnal, Khimiya, 1960, No. 21, P. 50, # 83983 AUTHORS: Tolstopyatova, A_A . Balandin, A. A. TITLE: The Determination of the'Energy of Banding-With Oxide Catalysts by the Kinetic Method for Developing a Theory of Catalyst Selection PERIODICAL: Probl.-kinetiki i-kataliza,,1960;'Vol.- 10, pp. 351-355 TEXT: The authors determined by the kinetic method the bonding energies of hydrogen, carbon,,and oxygen w1th various oxides and'showthat, In riccordanco with the theory, the molecular structure, the catalyst's nature, and the mode of the catalyst's preparation affect the values mentioned. Summary of the authors Translator's note: This is the full translation of the original Russian abotract. Card 1/1 S/062 60/000/010/019/031/XX B002/~060 AUTHORS: Balandin, A. A., Ferapontov, V. A., and Tolstopyat-ova, A.A. TITLE: Ability of Cadmium Oxide to Dehydrogenate Hydrocarbons by Catalysis PERIODICAL: Izvestiya Akademii nauk SSSR. Otdeleniye khimicheskikh nauk, 1960, No. 10, PP- 1751-1758 TEXT: The authors based on experimental work made on the dehydrogenation and dehydration of alcohols by means of oxides to make a theoretical study of the ability of beryllium oxide, magnesium oxide, zinc oxide, and cadmium oxide to dehydrogenate hydrocarbons. For this purpose, the activation energy was calculated on the basis of the multiplet theory (Table 1). The average value found for the adsorption potential of hydrocarbon dehydroge- nation was 51.3 for beryllium oxide, 70.7 for magnesium oxide, 116.2 for zinc oxide, and 132.3 kcal/male for cadmium oxide. The catalytic properties of cadmium oxide were studied experimentally. Cadmium oxide was synthesized by precipitating a cadmium nitrate solution with ammonia, and causing hydroxide to glow at 5000C in air free from CO and was examined by X-rays, 21 0 0 Dehydrogenation of cyclohexane was studied between 458 and 540 C (Table ~4. Card 1/2 Ability of Cadmium Oxide to Dehydrogenate S/062/60/000/010/019/031/XX Hydrocarbons by Catalysis B002/BO60 The reaction starts at 487 0C; at 5220C the catalyst is completely reduced, and dehydrogenation stops Dehydrogenation of cyclohexene to benzene takes place between 470 0 and 52~ 0C (Table 3 B). No cyclohexadiene is formed in this connection. Conversion of butylene to butadiene in nitrogen atmosphere takds place between 575 0 and 6050C (Table 4). The degree of conversion was 5 *6% at most. Conversion of piperidine to pyridine was examined between 4650 and 5200C (Table 5), and is believed to take 0place over piperideine. Metharie does not reduce cadmium oxide between 500 and 5950C. It wasconclud- ed from results that two different types of reactions take place: 1) a) C4H8 ), C4H6+ H 2 b) CdO + H 2 b Cd + H20 II) CdO + C 4H8 --4 Cd + H 20*+ C4H6 0. V. Krylov, S. Z. Roginskiy, and Ye. A. Pokina are mentioned. There are 1 figure, 5 tables, and 26 references.: 24 Soviet, 1 US, and 1 British. ASSOCIATION: Institut organicheskoy khimii im. N. D. Zelinskogo Akademii nauk SSSR (Institute of Organic Chemistry imeni N. D. Zelinskiy of the Academy of Sciences USSR) SUBMITTED: June 15, 1959 Card 2/2 S/062'/60/000/D 11 2,/-D02,~020 B013?BO55 AUTHORS: TITLE: Balandin, A. A., Jols~ppyptova A. A., Konenko, I. R. I---- -)-s--, -- - Investigation of Catalytic Transformations of Isopropyl Alcohol and Cyclic Hydrocarbons on Titanium Dioxide (Anatase) Using a Differential Thermocouple PERIODICAL: Izvestiya Akademii nauk SSSR. Otdeleniye khimicheskikh nauk, 1960, No. 12, pp. 2o96-2102 TEXT.: Zhe authors of the present paper investigated the dehydrogenation and dehydration of isopropyl alcohol (Tables 1-4) and the dehydrogenation and irreversible catalysis of hydrocarbons, cyclohexane (Table 5), cyclohexene (Tables 6 and 7) and 1,4-cyclohexadiene (Table 8) - on a modification of titanium dioxide (anatase) using a differential thermocouple (Chromel - cupr nickel). The latter had 10 junctions each at both sides of the mica sheet to which it was attached. All the 20 junctions were on the one half of the sheet. The distribution of the catalyst in the quartz tube containing the thermocouple is shown in Fig. 1. A continuous reaction vessel was used for the kinetic experiments (Refs- 4 and 5). The temperature was maintained with Card 1/3 Investigation of Catalytic Transformations of S/o6 6o/ooo/o12/002/020 Isopropyl Alcohol and Cyclic Hydrocarbons B013Y-11055 on Titanium Dioxide (Anatase) Using a Differential Thermocouple an accuracy of +50. The evolution rate and quantity of gaseous products were measured and recorded by a rr-n-lo (GSP-10) gas meter (Fig. 2). X-ray analy- sis of the catalyst prepared from titanium tetrachloride showed it to be anatase. The transformation of isopropyl alcohol on TiO 2 was accompanied by a marked change in thermal effect during the first 15-20 min(Table 1, Fig.3a). The analysis of the gaseous products formed in the reaction showed that the alcohol is practically only dehydrogenated during the first 7-8 min: After this period dehydrogenation and dehydration take place simultaneously and after 15-20 min dehydration occurs alone. From a comparison of the thermocouple data with the analytical data of the reaction products and t;:e degree of carbon deposition on the catalyst surface it can be seen that the rates of dehydrogenation and dehydration, and the carbon content of the surface run parallel. The change in selectivity at otherwise unchanged general activity of TO 2 is probably due to the acouinulation of carbon on the aiir- face. Deposition of carbon on the surface of Cr2 03 (Fig. 3b), however, was found to have no effeot on its activity and selectivity. Summarily, the Card 2/3 Investigation of Catalytic Transformations of S/0062/60/000/012/0,02/10,20 Isopropyl Alcohol and Cyclic Hydrocarbons B013/BO55 on Titanium Dioxide (Anatase) Using a Differential Thermocouple authors conclude that a gradual accumulation of carbon on the anatase sur- face almost entirely suppresses the dehydrogenation cif the alcohol -and promotes its dehydration, but does not affect the total activity of the catalyst. The catalyzed irreversible transformation of cyclohexene and cyclohexadiene is suppressed by the accumulation of carbon on TiO 2Y whereas the dehydrogenation of cyclohexene, cyclohexane, and cyclohexadiene is pro- moted by this process. There are 3 figures, 7 tables, and 12 Soviet references. ASSOCIATION: Institut organicheskoy khimii im. N. D. Zelinsko,go Akademi-i nauk SSSR (Institute of Organic Chemistry imeni N. D, Zelinskiy of the Academy of Sciences USSR) SUBMITTED: June 26, 1959 Card 3/3 B102016011341003103010331XX B004/Bo64 AUTHORS: Balandin, A. A-2 Academician, Tolstopyatova, A. A. and Stshizhevskiy~ V. TITLE: The Catalytic Activitylof Tungsten Pentoxide PERIODICAL: Doklady Akademii nauk SSSR, 1960, Vol. 134, No. 3, pp. 625 - 628 TEXT: The authors investigated the dehydration of ethanoll isopropanoli t-butanol, cyclohexanolg methanoll, and Tetralin7with -WO under iso- 11 1 2 5 thermal conditions. Blue W 205 was obtained from tungstic acid at 350 - 4000C in an air current. First, WO 3 was formed and then reduced to W205 during the reaction with the alcohols at 200 - 300 0C. The reaction apparatus operated continuouslyj and the liquid substances were auto- matically added. The gaseous products were collected in an automatic Patrikeyev gasometer, and analyzed with a BTM (VTI) apparatus or chroma- tographically, In the liquid product of catalysis, the amount of Card 1A The Catalytic Activity of Tungsten _c/020/60/I34/C03/C3O/C- .4 ~ VXX Pentoxide B004/BO64 unsaturated hydrocarbons was determined by the method of Kaufman-Gall-. pern. Since the endothermic effect of reaction affected the results of measurement, the catalyst was diluted in a ratio of 2 : 3 with quartz of the same grain size, the alcohol with water or with the corresponding unsaturated hydrocarbon. Under these conditions, the process was iso- thermal. By determining the apparent activation energy (Table 1) it was found that the primary alcohols were dehydrated with the same energies (approximately 30 kcal/mole), that the activation energy of the second- ary alcohols was about 6 kcal/mole lower than that of the primary ones, and that the activation energy of the tertiary alcohol was approximately 6 kcal/mole lower than 'that of the secondary ones. The reaction constant and the relative adsorption coefficients z2 and z3 of water and the un- saturated hydrocarbon were computed (Table 2) by Balandin's method (Ref. 3) with reference to the adsorption coefficient of alcohol. Check- ing by introduction of the experimental data into Balandin's equation confirmed the validity of this equation (Table 3), Table 4 gives the actual activation coefficients for isopropanol and n-butanol,, which are approximately 3 kcal/mole higher than the apparent ones. For the binding Card 2/4 The Catalytic Activity Pentoxide energies QHC, QCC, QOC face of W 205g the follDwing tion: Table 5: of Turgstrin S102q6011 34/003/C 30/C33'/jrX B004/BO64 of the H, C, and 0 atoms reacting with the sur- was computed from Balandin's kinetic equa- Alcohol Activation energy B i n d i n g e n e r g y of dehydration QHC QCC QOC - - - --- - - I~kcal/mol~j - - - - - - - - - - -- - - - - _ - - - - - - - - - n-butanol 29.9 56.7 15-9 39-2 ethanol 29-4 56-4 16.3 39.5 iso-propanol .23-7 52.3 19.4 43.3 cyclohexanol 21.9 51.5 21.3 44.4 t-butanol 17.8 48.7 24.0 47.3 Although the hydrogen atoms and the radicals substituting them do not directly take part in the reaction; Card 3/4 The Catalytic Activity of Tungsten 3/02o/6o/i 54/003/C3,O/C33/;rX Pentoxide B004/Bo64 H C-C (CH3)they affect the binding energy between the C; H, and 0 H I I H(CH3) 'atoms and the catalyst. The authors mention a paper by HffH H R 0 H 1. Ye. Adadurov and P. Ya. Krayniy._There are 5 tables and 8 Soviet ref-erences. ASSOCIATION: Moskovskiy gosudaretyennyy universitet im. M.V. Lomonosova (Moscow State University imeni M.V. Lomonoa-Qv) SUBMITTED: May 17, 1960 Card 4/4 TOLSTOPYATOVA, A.A.; BAIANDTH, A.A., alcademik; KONENKO, I.R. Catalytic conversions of alcohols and c7clic Yordrocarbone on titanium dioxide. Dokl.AN SSSR 133 no-1:130-133 J1 16o. WIRA. 13:7) 1. Institut orgunioheakoy khimii imeni N.D.Zelinakogo Akademii nauk SSSR. (Alcohols) (11ydrocarbons) (Titanium oxide) TOLSTUPYATOVA, A.A.; B&LUMN, A.A.; HATrUSHMO, V.Kh. Dehydrogenation of alcohols and cyclohezene on XnO, Izv.AX SSSR Otd.khim.nauk no-5'-787-793 MY '60- (MM 13:6) 1. Moskovskiy gosudaretvennyy universitet imeni M.Y.,Lomonosova i Inatitut organicheakoy khimii imeni N.D.Zolinakogo Akademii nauk SSSR. (Oyclohexene) (Oyclohexanol) (Isopropyl alcohol) VARI as 2t :1 u't -08 '6 All It r poll: V, d"'g i'll ;4 1 9'V4 p IRV C-4; ftf -f4t A is M:, f OF a 12 or 00 tag i F Af TOLSTOFUTOVA, N.S._Jjeningrad, P-49, ul. Lizy Ghaykinoy, d.18,, kv.1) Occupational epicondylitis of the arm. Vest. rent. i rad. 36 no-5: 46-51 S-0 161. -r- -- 0'1IRA 15:1) 1. 1z rentgenologicheskogo otdeleniya (rukovoditell - prof. A.V. Grinberg) Leningradskogo nauchno-issledovateltakoCo instituta gigiyeny tcuda i professionallnykh zabolevaniy (dir. - prof. Z.E.Grigorlyev). (ELBOW-DISEASES) (OCCUPATIONAL DISEASES) TOLSTOPYITOVA, R. V, Work experience with parafin in the preparation of orthopedic apparatus. Mad. sestra, Mosk7a no. 9:29-30 1951 (CUL 21:1) 1 1. Author is'a plaster-of-paris cast technician belonging to the Bone Division (Head -- A.P. Sokol'skaya) of Ivanovo Oblast Tuberculosis Sanatorium No 2 (Head Physician -- Honored Physician RSFSR A. L. Gallperin). 157 j-~ 00 6 6 0 BOV/20-129-4-22/68 AUTHORS: Balandin, A,A,, Academioianp Karpeyskaya, Ye.Iop Tolstopyatova, 'j A. A* TITLE: On the Irreversible Catalysis in the Presence of Metallic Rheniu~_l PERIODICAL: Doklady Akademii nauk SSSR9 1959, Vol 129, Nr 4, PP 795-798 (USSR) ABSTRACT: Metallic rhenium, applied to active carbon dehydrogenates the cyclic 6-membered hydrocarbons. On an ammonium perrhenate (Re-1) Catalyst1small quantities of cyclohexene and-also benzene are produced from cyclohexane (Ref 3). This is not the case on a catalyst of a dioxane complex of rhenium-acid-anhydride (Re-2). The authors investigated the transformation of cyclohexeneqon Re-1 and Re-2 to find the reasons for cyclohexene lormation on Re-1. Moreover, the capability of rhenium to bring about irreversible Catalysis (expression by N.D* Zelinskiy) was to be investigated. The gaseous reaction products were collected in the gasometer by V.V. Patrikeyev They consisted of hydrogen with 6-8% methane. The experiments were made between 215*and 4650C.Por both catalysts a temperature range was distinotly observable in which no gas is formed and the process takes place according to equation Card 1/3 3C6910 ~ C6H6 +2C6H12 . At higher temperatures hydrogen is separated, 67260 On the Irreversible Catalysis in the Presence of SOV/20-129-4-22/68 Metallic Rhenium Catalyeates of several experiments with Re-1 and Re-2 were poured together. After the removal of the incompletely reacted oyclo- hexene benzene was chromatographically separated from cyclohexane. Figures I and 2 show the results of various experiments which were well reproducible. It may be seen from a comparison of the kinetic data on dehydrogenationlof oyclohexene and the disproportionation of hydrogen on Re-1 and Re-2 that the activation energies of the processes aro in agreement on both catalys"U-s. Apparently both processes stop at the same stage of reaction. Table 3 shows that on Re-2 benzene is formed from cyclohexene twice as rapidly as from cyclohexane. According to M. Yao Kagan and IN. A. Shcheglova (Ref 6) cyclohexane is dehydrogenated on Pt by 4500 times more slowly than is the transformation rate of cyclohexene. On the basis of these data and according to bl. Ya. Kagan and R. Y. Flid (Ref 7) the mentioned researchers draw the conclusion that the dehydrogenation of the cyclic hydrocarbons takes place step-wise (see Scheme). The results obtained by the authors are in contradiction with this conclusion: cyclohexane is deby'drogonated on rhenium not according to a step-mechanism but according to a sextet mechanism. Benzene Card 2/3 was formed on Re-1 from cyclohexene about twice as rapidly (Table On the lrraveroihie Catalysis in the Prooence of Metallic Rhenium. 6 72 U_ 0 SOV/20-129-4-22/68 It may hardly be assumed that the dehydrogenation of cyclohexane on two catalysts of the same chemical properties and on the same carrier should proceed according to two different mechanisms. Cyclohexene is no intermediate (in contradiction to the scheme of references 6P 7) since it was not obtained in the reaction on Re-2. Cyolohexene thus results from a side-reaction which takes place to a small degree besides the sextet dehydrogenation. There are 2 figures, 4 tables, and 8 referencest 7 of which are Soviet, ASSOCIAT.'ON: Institut organicheskoy khimii im, N. D. Zelinskogo Akademii nauk SSSR (Institute of Organic Chemistry imeni N.D. Zelinskiy of th Academy of Sciences, US SUBMITTEDs July 24, 1959 Card 3/3 VIKSNE, A.; VIL%WE, J.; DEVISOVA, U. (translator]; KASPARSONA, G. [translator] LEGZDINA Zh. [L-erzdina, Z.) [translator); POISHA, Ya. tpoisa., J.j (tranala'tor]; TOLSTOPYgO-Y".- [translatori; ALKEKE, B.,, red.; BERZ3NA, K., red.; SILDIS,V.j, tekhn. red. [Riga Zoological Garden] Rizhskii zoologicheskii sad. Riga, Latvijas Valets izdevnieciba, 1957. 1 v. (chiefly illus). (MIRA 14:12) (Itiga-Zoological gardens) TOLSTOSHRY. A.V., student V kursa OMF Methods of testing central photographic shutters. Trud7 141IGAIX no.36:117-122 '59- (MIRA. 13:4 1. Studencbeskove naucbnoye obsbebestvo Mookovskogo instituta inzhenerov gaodezii, aerofo oa".vemki i kartografil. (Shutter, Photographic--Testing) TOLSTOSHEYY A,N., assistenl~ Analytical method 1~ . i,~,,,Ixmining the basic norms for swit'Obing operations. Mauch.tru-jy KHIIT no.55:39-50 62. Device for recording the parameters of the movement of switcher locomotives (electric switcher recorder). 81-87 (MIRA 16:10) KONIKOVY P.S.P ~ kand. tekhn.nauk, dote.; DONTSOV, A.Ya., inzh.; YURCHENKO, I.F., 1nzh.;-ANGELSYY.0, V.I., retsenzent; BABENKO, V.I., retsenzent; ZAPREVSKIY, G.S., retsenzent; KRDINUS, G.Kh., retsenzent; MANIN,-I.I., retsenzent; NAUMOV, G.K., retsennent; TOLSTOSHEY IA.N., retsenzent; TUCHKEVICH, T.M., retsenzent; FEDUMTS, Y.M., retsenzent; FELIDMAN, M.F., retsenzent; FRANKOV, N.Ya., retsenzent; USENKOI L.A., tekhn. red. (Establishing work norms in railroad transportation] Tekh- nicheskoe normirovanie truda na zheleznodorezhnom transporte. Moskva, Transsheldorizdat, 1963. 366 p. (MIRA 16:9) (Railroads-Production standards) LF,BEDEVA, A.P.; TOLSTOSHEI.- O.N- on of soil with hexachloran from its use in agriculture. Contaminati 04IRA 1/,:11) Gigj i san. 26 no.3-1:15-18 N 161. 1z Ukrainskogo nauchno-issledovatellskogo instituts. komunal'nOY gigiyeny. (CYCLOEMYXE) (SOIL POLLUrION) TOLSTOSHEr. 0.H. Enlarged conference on sanitary protection of the sea near the shoreline. (;Ig. I san. 24 no,1:88-89 Ja '59. (MIRA 12--2) (SBA WATER-POLWTIOII) BARAN, N.A.; TOLSTOSERY, O.N. Hygienic problems of sewage and waste disposal in towns of the Donets Basin [with summary in ftlish], Gig. i sane 24 noo2:22-26 7 159. (MIRA 12:3) 1. Iz Ukrainskogo, nauchno-iouledovatellskogo instituta kommunallnoy gigiyany. (SANITATION hyg. problems of sewage & waste disposal of towns of Donbas (Rue)) TOISTOSHEY, O.N. '-'4,vgienic featuret3 of garbage disposal in Kiev. Grig. i sart. 23 no.12:60- 62 D 158. WRA 12: 1 ) I Iz Ukrainskogo nauchno-isaledovatellskogo instituta komimmallnoy gigiyeny. (SAMITATIOt- garbage disposal in Russia (Rus)) . TOLSTOSHRY. O.N. Wyev) Significance of a regular trash pick-up ser7ice for the public health in cities* Vrach.delo no.6*621-624 Je '58 "'PIRA 11:71 1; UkrainsKy institut kmmmumnllnoY gigiYeavo AUD MITUSE DISPOSAL) TITLE, 54tenttric-tuchnt~.1 C-f4r'Au' of t-le I X In 1959 (N.-b-%.khnICh..k.Sa UITU 1 9 M9 PUZOUXULl Ixv**ti,a wyoohLkh uchabn.Ykh Z%Vwdtr.11. ro'o04oxIXA I aor.f.t..-- C> yeake, 1959, Xr 3. pp 144 - 146 (034) LUTRACT. Th. periodic dal.Atifia-t.ohni.al 0.0f.r..O. Of the laotit.t insh.n.rov 1.0d.ZLL, I kortografli (VQ0QOw Institute of Geodetic. Aerial Survey and Cartoljmphic So4inoors) was held of. April 22-24, 1759. with the partialps- $ion of 500 persons. 31 lecture. *or* delivered. Th. I.tr.- ductory speech was hold by Proro.oor a. A. liatov. Canditsta of Philosophical Sciences A._L._,LYJjX2' lactir.4 on -The Out. C_ Standing Work Of Materialistic Ph1l..;pbi*i Candidate of T..A- steel act*".. I. T. lonarombkov on -4 G-- 4" C4 didt. OrT.Mrc-l a G~~ 1. Ragrotimi On "Aa4uracy of the Solution of the laver.# position Computation th Coordinates of Different Geodetic Sy.S.Ra-I Condidato, of W ,no Joel Sciences P. Y. 3hQkJA reported am ~Qravlmwtr7 in !. card Today-* U.S. of D~vilijmo.t-j Can4ldst. of Technical Sol*-.. - malm~ af the Rules 06vernIng 1"Q1!Ah1"_'i6 *1nvsCt19At1cR Uatrib.t-ta. of Irrare Than C*a.r&ljzjag %he golLsf in phat, grOphyal ro-t-grad"to Student to. 1. Mokb.. on ?be Jorl *-. _ of the Rounding Zrt`or on the APiio~~j ~CiZTttonm of U.- Zq%AtiOA SYG%4"". p*%t-6rLdUat* Student 1,k~ PI:9,4* "period .on llh aSolatIcA of Sys$." 1, be Co.po"Ation of Co.- i dot.is'- Docent 1, X, KoUlfv"ov, dealt with -The Uporl~nce, ; ' is the JLppI1OLt1%Q at pmr%llsQtJQ r; jygamaoatry With Short 3400 Od Cozst '- Doctor Of Physical and hath.- at Vertical Basis :'~ a mail a I no A. V. Fayasillb.rg lectured an 'Son. Integral. : Froo, the Theory Lppltzation to the Me. ohonla. of Artificial Earth S.t.llltoa~l Candidate of Tochal"I S11Gn4*4 A- S. VAIR" on -The Itoreocomparator With Correctors-. A-G1_Gts--Q9_-_r-.-Nr., Wt. on -7hatosr-ma-t-la U-thoa of us- UrRIA104 9E_eTTUVuu4o8 or Luminous Claude-. Candidate of Tech. n1c6l U16MG49 on -The Contrail--- tJQ1 Of the FOrm-la* far th. 11. Sarvol 4ut& %he &1t& ..a rl '. C. 1"I A Sure."d f Sol.."$ 4,-JL- ol 4 d C--didt- Of T.chnl..& Sales... N. P. Z;Ak.j... lo i Cazd 2/5 r.p. 1', 1. Send Tjrp- L.rL.1 _iz~ - R_ : _SiJel =_ Sciences B. N. Rodlonav spoke an the 63trabo oplo Collimator I~J-IAXXha3 rt;orlod OR &~Catit& Geer for the Antomatic "%ry of the Airplane :;, to tb* Aerial Photography Path-. Post-graduate Student ~~ ~i. luen.t.a. "OpiloAtIon of the Inotanta...- Photo- th I n : =* o gr%phy for& 11.1"r. 2 it.&,. e spoke an the -Computation Of the Aerial Co.* I an. ~N Chief T.chul.1.6 or the Cootkhboator% *- ClcGP3m-- TdM GO'So.. and Teel. &stated to Phot at" dOl1t4 342's-ying Operstionawl Doctor of 2achalcoa SOL*.. : OTh Problem Cono.rALU the Content* of the lo 3o.1 or 0 000*, D-*., .1 1.ab.,c.1 : th 2 2, 11 _1,-Exg W an *vLawral Deposit- In the 0552 S.Iona..-A, br,~ 1 and Th* ir Ropro4uctton an Economic tUpo-; Assistant 0. _x2JA_. the method of Geographic Ino..i1gti.. on th During the Preparatory Editorial Work am the Cart " phhe . Object (prom the Working Zzy.rionco Acquired by tT. r.- key. (NaLloborrlay% Empeditsom, of the MIX" 1 1 1955)-. ' ifit at AM -olt with ~rb. Problem r Y, _ * ` A ' 2 ' 'K I o d Ptcv1V1 Sh ~ iA11 4 - h tLon of a list '-b1t.. f - v4 Pr Xm it.ry t he Upodr.phic Key On the Scale of I - 10000'. C..dldt* T ochnic.l 3cion.., poke " _MPV QC C-Iti~.twd ~~ Lr..a In the CROPrah.R of the Candidate of Technical Sciences _L -1. Men txhtka, dosal oLth 'A. 3. Popov - _ 5_im-f_(0_Q_tb- 1001b Birthday a t . I ... agar. 7- do LoDtl: "i- o 1. 0.p,)". Scalar I.Outror x 1-.t.r.d a. ' "Mirror 1,eas Objectives with - Prof ... or 11 ' 1 Sfirlf of C"pecoatin, l the Tarta- o: :: n ;o ; and . . , A racy 1. the Of ph,. f T.ch.lo.1 Sets.... T. AL . C.:did.t. _ArA=_ ' r_ '; aaL!ZAL dealt it; 'M thuds Measuring J.v "tlaA t or. Can- corn Ing Optical Main Charoct.ri.tI.s of Aerial Comers ObjeotIvem uth Dropping Atmospheric Prosoure and Towporstar*-. Xndlneor loc~ur*d on -Vertical A 11. 3y.t.- of 914h-rr.. oisl-n Optical Theodolites-. A,wl.t..1 spoke On * I h. .1 5 A-4 by the Lid of Telescopes With Z.A. pl.t..-. past_ 4 - -1 1 A.Iza , ?. P! Z4Xh,r,1 dealt 111 l gr :-I t * of Card 4/~ _ : :: . : ! o: art a ?air of Stereoscopic P.r ALt hary ~ b h-14 an April 24 the Chief or the Cl-.y. up, '1 * " ' t Ikartograrit XYD SSSR (Chief Ad~laixtratw. N 1 . '~ deep and C. rtography of the Ministry of I.t.r.al Affairs of th: U53")-A,11~Urmrov lectured On *?he Swvsn-y,ar Plan &cd th D ... -bt of Topoir pL1c_S,,odqt1c ead Cartographic %.rk.. 3(2).3(4) AVMM1 so" Gi~vwu SOT/6-59-6-21/22 VITUS chronicle (Khrovik.) PZXXODICLL, Goodastys. I ka~~ogrsfjs. 1959. Nr 6, Vp 74-75 (USSR) ANSTRAC?$ At the Koskovskly inatitut Inshenerow goodoxii, aorofotonoyeaki I kartogragIl (Moscow Institute of Geodetic, Aerial Survey and Ce.rtographia Inenears)o the Ordinary Scientific Conference took place an April 22-24-- A. 1. Docent, Candidate of Philosophic Sciences, spoke cn "The. Outstanding Work of latarlali.tlo Philosaphy% A. N. BarecOv. Chief of the Glavuays upravlanlye good*xii I kartografli (VAin Admilvalstration of Geodesy and Cartography) spoke "On the Satvo~yesr Plan for the .11 -lopment of Top graptic.good.tic and Cartographic Work* *Tb* 1.1lowIng rsports :or. delivered in the geodetic sections A. X. Payvallfbar. Profeasor,"Soms integral. of the Surface Th. reas &ad Their Application to the Mechanics Of Ax-tiflals.1 3=11itas of the Urth-.- A. T. Kondrm.hk.,v, Docent, *BAdjo. electronics and Osadoay-.- G TV. B-a-to-L, Docent, "Accuracy the Solution of Inverse ;;.Ittau Computal-c" by the f Different Goodqtlo SZoteasQ.- tt ?-P kin a C _2, _ -Grmvi-tr7 in the Pro.*.' ~ts. of D.T.1o;.*SSt-.-Y Assistant, "ported OIL the infliewi of rounding error& on the socar cy of solution of linaLr,aluati- ayst2ma.-T, Djal'sh C--41::ta of Technical Satenoom, spQko on the oravestigation the Roa a of Distribution of Errore in Gonaralistag tho 12611st LAS VrUdo~ P)4t-g-.dUit. Std.ot, reported an I 81 I tion of *-Locar ysta.. far the adjustment of p.datio u :0 1. 1k s. 7. X. do .... t-t.d an Apparatus ;;7 do signed him far POVL114".1- trs7sraLng elth a short on "Lane vertical bas!&.- The fol?av-na r,;iorts ware d.1--vored in the 40-pbotog.od.-Io oootio., A,_%_yAj4a~ax, Docent. "ported on & parallactic roductr, an ad&-Itlaral lariao to the stereo. acispax.tor.- ~ D~'ant. eyoko an the possibility Of 96"MILS,149 the formulas for the air suroeY of Outlines and wT--oA I P Zskazn~v, Docents, "ported B. 1. R.dI -- an & %id-hap. Sihutt.r-Tc-r-&-~-. =aossiora., R- Radio=, an SS at"Soo-pia eight, 3. S. Radio-- anA - -2SjM L. Yorkhov on the .*home o; a computing device for ar X, _ the automatic ntr7 of the airplane, -Into the rants tar air survoya 11. P. hanLy pr*sauted pass Simplifications for the _Are Card 2/4 j compute tar. of c3nat "-Ts of sarlov! ................ it..:~sdoats Student, spoke an the use of rapid filo'recarung for *be IcwS&t-.Sstjou of -rjal-oamora shuttors-r-T -G-1.bL1vlj c. 3p,.= RSYSR. spoke ICA sones r of the coo takhkontom M41m t Masult and Tasks In the rtvl~ Ica Of LLrg-----l- Photo' : thoodol4to SurS,.ys'.- Th. fall--ind ro;orts -.ra dftli-rOd 1% tha asriagraphlo saiat.'an, T. 1. Skhay spoke an the - FY,%5,000- Professor I content of the ne. may a..!. of nskiy spoke on 'Iduartl R-scw--- Of the VSU aS;h r*c b r intitt'a a Z~'=.!l M-ps'.- I,- rpr. - d'k2- ,; : !L VE: X vothad of gooera;hio field researth on th. Assistant, reported during -he p_p_&t r7 .11 1., e.,k at ho object of , c asritcgrvphy~ Assistant, reported a- tL. l ~~ l ,.Ntinz of wooded flat country on t f I.Yr.vezont oAk the topographic map .0 . so.,-* of I , 10,000.- Tn. 3. Bill.h. A.&I t, "ported on are of pertzoat t rof %he Oblast'- In the section of building of &%U% syparatue, 1. 1. X~!a,V-L~a- D-ont, o2ok. or. the life Of reported an rafl#otlug a '. accuracy im as tb. lu~ CrZI as r M. SS.-q, on -rtical "W systems for highly 'pt th.. d~ -1 1 t", T, S. a", C ard 1/4 plat Assistant. a- ightj1g ith with Sao* - P. P. Zakh.ra,, Assl.tan', ~. th, of "r. O.PI-. TOLSTOUIWOV, A.S. Practice of jonducting P, vestigatior4s. Geod. i - Ii2llna~ topo~phic and 98~~ic ir . Kart- BO,2:49-53., 1639 (Topographic mapj- (MIRA 16-3) AUTHOR: Tolstoukhov. A. S.- Graduate Student S ro~,, / I TITLE: Some Peculiarities in Representing the Relief of Plains on Topographic Maps on a Scale of 1 : 10 000 - Shown in thle Case of the Terek Delta (ITekotoryye osobennosti izobi-azheniya ravninnogo rellyefa na topograficheskikh kartakh z:.~asshtaba 1 : 10 000 - na primere dellty reki Tereka) PERIODICAL: Izvestiya vysshikh uchebnykh zavedeniy. Geodpzi,~,-a J. aerr- fotos"yemka, 1958. 1Tr 1, pp 123-131 (USSR) ABSTRACT: Topographic maps are used to a large extent in studying the characteristics of various geographical areas in the USSR. This is true especially of maps on a scale of I : 10 000. These maps in use today do,horiever, no longer meet all re-. quirements. Above all, the representation of the relief with the micro-forms in the plains on topographic maps (large scale has not yet been SUff~C4 ently developed. 'he au-chor and his collaboratoistherefore selected the delta of the Terek River for their investigations. One of the -oacuifari- ties amongst others of the delta is the elevated position of the central river bed in the delta (up to four meters). Card 1/3 On both sides of ',-his river bed the terrain gradually fails. SOV/1 54-56 16/22 Some Peculiarities in Pepresenting the -Relief of Plains or, S - -e Terek Da' ;T.aps on a Scale of 1 : 10 000 houn in the Case of th Ira The numerous other branches of the Terek therefore are situaT- ed lover than the central river bed. innumerable small eleva-, tions, dome-shaped and overgrown, are characterlcti3 of -11-nis delta region, as well as the amorphous salt soil. The author discusses in detail the methodsof relief representati(;n de.- veloped by him. The combination of the micro rel--ef (the Uound with small dome-shaped elevations), of the flora on the one hand and of the semi-arid area on the oth,~r hand, requires a comprehensive and uniform representaz~ion. ~?he author proposes new topographic sy-pbols as i3arks of the small. dome-shaped elevations. With respect to the flora the auther sugggests the method already developed by K. A. Borodira. The elevation marks and fig-ores should be printed on topo. graphic maps in a way that they fbIlow the turns of the con- tours. The present density of topographic marks within one square decimeter has been insufficient and shoald therefore be increased considerably. There are II-I fi,-,ures and 5 ret'-- Card 2/3 erences, 5 of which are Soviet. SOV/154-513- 1 -16/22 Some Peculiarities in Repres'enting t~ic~ Relief of Plains on Mlaps on a Scale of I : 10 000 - Shown in the Case of the Terek Delta I e k . I ASSOCIATION: Iloskovskiy institut inzhenerov Geodezii, aerofot086 y M,4 ,kartografii (roscow L-ngineering Institute of Geodesy, Aeroplictogiaphy, and Cartography) Card 3/3 "Maoxg Sollaftko.. V. D.. Canclid.t. of Technical Set .... 4 TITLAa Saleatific sad T"hntc&l Conference of the MI!GA 1 9 (M..chno- takhatobaskaya konforentalys NIIG4 I K) It FERIODICAL& Isweettya y..jktkn uch.boyich zxvdaniy~ Q.odvz1YL I aa,rofotc.1y*m". 1958, Ir 2. Vp (U9.ig) A05TR4Cr. 0, A. Gtn1b-,, DQG..z. Candl4ato or Technical Scivaces. spews an Th: 9.1allood, Between Distortion* in Cartographic Prnjec- L L Badc. C n4joate or Technical ftclett-~sm. re- tl. A ' port;i *T pagrapht D v bft-%v4 From to# Airplane and ; alp ILeapter at Aerial Phatographe In Cartographing Inaccessible 4 : 1 , 'a-*' * -1 Ilto4khll, 0.1i.r Reprod o"Krvi,c. I 1 10 000 000).~ 0. D. likhtar. Professor, Doctor of C.ograph. troct%r. of lost Oal a"* Isalt ith th* ba&L hic a geo gra :: o:4 u h u ...... 91 and he cq on, .., .11 1. 1 pea liarition or p :g the real on. Ledia..r To. U. Toklistay reported on the conforrucs held to the UTICA IIt (Moscow, toaln..ring r C.co..y, k.-- Card 115 photography. asut Cartography) fros, Way 6 to 10. The part%cl. pan& discussed various qaeatio" In relation with the damiga L at a detical a" cartogrophical tastrustenta. Kore than 3C0 fram away universLtit. " scientific XnotltaLLone. 401:6ates s " it . 02 repreavatatives or different agoncleA to Lenin rad S ardLovalL, and other wti-ip-tat in ' ILLS ' a :Dnf : :: blo orefto Th D4pugy Uesd of the COCK# W. D. Koo-mhlu. "ci.n1ific Raw V-4 a pap ws,rmn 1. A.ri.1 Cast- :r .. 3. T *, -se Coosa, , "'0 "" .. " present "1.%. of Pro- . d409. or Irueents. and Development of New, To- eats.. Dr-by now, Profeamor. gave a Itcture *a taw t rids I instrument. In tn. U. IR .04 on dew, ts - 4 0 n 1 * , 4 1 0 t t c 1 r 1 " p q lh "' 121 l 11" !Q r ,I.= r t la t rb . 1 mt :i 1. L * t . . 4 nd phot M r I " a D% 1 I a g . ,am "s am mail &A t" LMmv4zs for aerial phoLogmpny were trux: ,,, : 4 -0- *at f- 1. Y I.-Ye, and E.Sln,.r .., T. Z4.bnzk.e -: report a ang I- 4 a 0e04 1 1.,..~rur I=C trusents. gn4in- ~. V, Resbc Ith the new Zrw1I1wyd 1-1~6 r b::7 C dat es. .4 Ma.r. Technical 1.1 ; ;. range finders of greater precision. V. a. Vatichko. CA"%4a-- of ?.Chat CI Saiwaicos, an optical range finders of mo4zua .c- Card ?I, ~: M. cy. KndI:_r I- I. A.drl&no,a sod To. P. F.ptv. C-'dd. aI pOk. .0 madal.t.r. of optical ftyst"l-Hathaftet.a.l. so t*UOA. ;.: range finders. X^S I .. r L. V. zzo,ich spoke an the us. Or Itot alloys in tn* manatecture of geodetical Instruments. lkoe-at S. U. Mira4aw and Zadinewt, T. K. Sy..ka rapt,%.d yr.ductLas, Of geodetical instruument.. mem, developments to th :, C-Ip ..It 'it' he opt "st"t" to loa l Prof , I I ngirtear b. A. L am*dot a truseen .. ... r 1. I. r.9o .t T. A. Krt,mwli., r;*.wswz 1. X. Firson. ad Eruqx.... Sh Alin, Dcc p- rticipoints on the results Of Ch. Vshk , Info-od th A. : SOL tific sad Techni 041nf.r.-. held 1. Kly., (Planning and L ;o production or 0"44tical Card 5/5 TOI~QTOUKILIOIFI A. S., Ass't. "On the Representation of Re-liefs of Plane Areas on Topographic Maps" report presented at a Scientific-Technical Conference at Moscow Inst. of Geodesy, Aerial Photography and Cartography Engineers, 24-26 April 1958. (Geodeziya i kartografiya, no. 6, PP. 79-80, 1958) op irs nt Certain peculiarities in representing lowland relief on topographic maps as exemplified by the Terek Delta. Izv. vys. ucheb. zav.; geod. i aorof. no. 1:123-131 158. (MERA 11:7) 1. Moskovakiy institut inzhenerov geodezii, aerofotoa*yemki i kartograf ii. (Terek Valley--Topogreihical surveying) TOLSTOUKIIOVA., L.I.; BYKIIQVSKAYA, A.M. 1-131 treatment of pootoperative rocurrencoo of thyrotaxi- coois. Viod.rad. 7 no,11.5-9 14162. (14IRA 16:9) 1. Iz kafedry reptgenologii i radiologii (zav# - profo Ye.L. Kevesh) Kuybyshevskogo meditsinskogo instituta. (HYPERTHYROIDISM) (IODBfL ISOTOM-TIIERAPEUrIC USE) UZRANSKIY. Ys.G., prof.. XACHANOVA. S.0., dote., T0LSTOUKKOVA,.LI*.dots. , Fifth conference of the Ural branch of the All-Union Society of Pathaphysiologists, Pat.fiziol. i ekspeterap 2 noJt&J-62 MY-Jf- 158 (MIRA 11M (PHYSTOLOGY, PATHOLOGICAL) UZHANSKIY, Ta.G., Drofesnor, iDredeedatell pravleniyL4 TOLSTOUKHOVA, L.I., dotsent. sekretart. At the Ural branch of the All-Union Society of Pathophysiologists; on the organization and the first conference of the Ural branch of the All-Union Society of Patheiphysiologists. Arkh.pat. 15 no.2:90-92 Mr-Ap '53. (MI-RA 6:5 1. Ural.!,Bkiy filial Vaesoyuznogo obshchestva patofiziologav. (U]~al Mountain Region--Physiology, Pathological) (Medical societies) BYKHOVSKAYA, A.M.;_TqIZTOUKHOVAl L.I. Treatment of tbyrotaxicosis with radioactive iodine. Med. red. 8 no.12:9-13 D 163. (MIRA 17:8) 1. Iz kafedry rentgenologii i radiologii (zav. - prof. Ye.L. Kevesh) Kuybyghevskogo maditsinskogo instituta. UZHANSKIY, Ya.G., professor, predsedatell; TOISTOUKHOTA, L.I., doteent. sekratar'. Second conference of the Ural Branch of the All-Union SOciet7 Of Pathophysiol gists. Arkh.pat. 15 n0-3:88-90 My-Je 153. (MLRA 6:11) 1. Pravleniye Urallskogo filiala. Vaesoyuznogo obahchestva patofiziologov. (Ural Mountain region-Patholov-Societies) (Sooieties--Pathology- Ural Mountain region) (Ural Mountain region--Physiology--Societies) (Societies--Physiology--Ural Mountain region) TOTSTOLIEHOVI A. S.: m)Aer Tech Sci (diss) -- '~RepreBentation of relief of a lawland plain on topographic mapfj on a acale of 1:10,000 (on the c)xnrrtp'.L,.) of the &elta of the river Terek)". Moscaw, 1958. 15 pp (Min Fip er Educ USSR, :h Moscow Tnut of Engimorfi of (Iloodaily, Anrial, Phol-,o(traphy, nnd Clart,()P-rnphy), 150 coPieB (KL, jqo 2, 19r .)q, 123) TOLSTOUKHOV, A.S. ...j .......................- Editing tasks in the representation of flatland reliefs on 1:10,000 scale topographic maps. Geod.i kart. no.9:61-67 S '57. (MIRA 10:11) (Relief maps) (Topogrn-ohical drawing) - - .. - . I -- . 11 ~ . - ~ . - T-OLSTOUSOV, V. F., Cand Agric Sci (diss) -- "Ibe Soils of the YeLan,-Kolemovskiy .1 - - ___ - sugar-beet sovkhoz, Voronezh Oblast: their genesis, properties, and ways of inereasir4q, their fertility". 'Voronezh, 19160. 22 pp (Min k-ric RSFSR, Voronezh Agric Inst), 150 copies (K.L, No 11, 10,60, 136) TOLSTOUSOV, V.P. Ways of increasing the fertility of brown Solonetz-type spots of the Chernozem complex. Fochvovedenie no.10:102-107 160. (MIRA 13:10) 1. Voronezhakly vellskokhozyaystvenrWy institut. (Solonets soils) (Soil fertility) USSR/Soil Science - Genesis and Ge-,Lwaphy of Soils. Abs Tour Ref Zhur Diol., No 22, 1958, 99985 Auth-or Talstousov, V.P. Inst : VDronezh ALTicultural Institute Title : Characteristics of the Soil Cover -of Yelant-Kolanov Su.~pr Deet State Faru :)ftthe Vorone7liskayn Oblast' in Conjaection wi',-h To_7,oLxaphy of the Area. Ori_r Pub : Zap. Voronezlisk. s.-kh. in-ta, 1957, 27, No 2, 339-342 Abstract : Yelan'-KDlinov SuCar Deet State Farm is situated in the eastern part of the Voronezhskaya Oblast'. Here soil- forLntion rocks exhibit a considerable influence on the character of soil formatim . VionE; the fomer predor.-Li- nate the parti-colored soft rocks, usually the salt- coutainin- sea de-- L, posits of the Tertiary AL:e. The sAl cover of the described territory, a plateau with a Card 1/2 - 16 - TOLSTOLSOVA, Z. A. A. A. KOF-tV, MSR 69,941, Dec. 31, 1947 TOLSTOUSOVA, Z. A. 23348 Tsellyuloznyy liesmyvayemyy Appret L i Ego Primeneniye. Tekstil, Prom-St', 1949, No. 6, o. 23-25.