SCIENTIFIC ABSTRACT BRAYNIN, V. N. - BRAYNINA, K. Z.

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December 31, 1967
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KARTSEV, Ye.B., inzh.j VOYNOV, Ye.S., inzh.; BRAYNIN, V.N., t--khnik Mechanized departments of welding and flame machining of metals. [Trudy]LMZ no.11:83-98 164. (MIRA 17:12) RABOTNOV, B.A., inzh,; BRAY11IN 1'.N. tekhn ~! k- Semiautomatic welding In carbon dioxide, (TrudyJIVZ no.11:99-108 164. (MIRA 17:12) RAZUMAYEVA, V.I* [trams:Lator]LJMAYUIH,-jv-,I. [translator]; YARISHE7SKIYO V.M.t inzh., red.; SOK6LISKIY, I.F., r-eF.Tzd-va; GOLIBERG, T.M., tekbn.red. [Glass in construction] 'Steklo v stroitel'stve; abornik statei. Pod red. V.M.Unishevskogo, Moskvaq Gosoizd-vo lit-ry po stroit.y arkhit. i stroit.materialam, 1961. 175 p. Translated from the Czech. (MIRA 14:6) (Glass construction) BRAYNIN, -&�., prepodavatel I Periarteritis nodosa as one of Ithe variants of collagen disease, Zdrav. Belor. 5 no.9:66-68 S 59. (MIRA 12:12) 1. Mogilevskoye meditsinskoye uchilishche. (ARTNRIES-DISEASES) (COLIAGO DISEASES) BRAYNIN, 2,9. alliil~jensary oC the 1,1092' "OV -a js I BRAYNINA, A.Lo Successful therapy of a case of Still-Felty's disease by splonectonv [with summary in English, p.631- Probl.gamat. i perel.krovi 4 n0.2: 55-56 IF 159. (MMA 12:2) 1. 1z terapev-ticheskogo otdeleniya. (zav. M.P. Redlikh) Vladimir- skoy oblastuoy bollnitsy (glavnyy vrach N.S. Aloveva). (SP3~m, surgery, excis. in Still Felty's synd. (RUB)) (ARTEIRITTS, IMMUMATOID, surgeri, splenectomy in Still-Felty's synd. (RUB)) ZHEELITBOVSKPYA, K~V.-, P~R~AYQNA ~Dj ~ Separation method for the removal of microfa-una from Quater-na-ri rocks Lsinr ,3 heavy medlum PP-3. Paloent. zhur, no,4,,.101-103 164, (MTRA 1?,,~ ~) 1, Pyatoye geologi.cheakoye upravleruye Gosudarstvpnnogo geolor4.- C, Chels;r0go konltcta ",.SSR. RUDASHEVSKIY, S.Ye.; BRAYNINA, E.G.; GUSELINIKOVA, K.G.; STEPUSHKINA, T.A. Physiological rest and stimulation of spinal centers. VestAGU 15 no.21:137-149 160, (MBA 14 OW (Spinal cord) (Electrophysiology) BRAY-NINA, B. Ya N15 917.m Konstantin Fedin. Moskva,, Izd vo "Znaniye", 1954. qf2bS 29 p. 817101 tural analysis the sample contained metallic iron and manganous oxide. S/020/60/132/05/28/069 11~ IWO BO11[B126 AUTHORS: Zhuravleva, X. G., Chufarov, G. I., Corresponding Member AS USSR, Brmina, D. Z. TITLE: Reduction of Manganese Verrite by Hydrogen and Graphite PERIODICAL: Doklady Akademii nauk SSSR9 196o, Vol- 132, Noo 5s, pp. 1074 - 1077 TEXTz The authors carried out the above reduction by hydrogen in a closed apparatus with gas circulation. The reduction rate of ferrite rises as the reduction progressee and reaches a maximum at about 30-40% oxygen removal (Figo 1). The reduction then slows down and comes prac- tically to a halt after removal of 75% 0 According to X-ray-struc- .F 2* The use of graphite powder in a vacuum of about 10-2 mm caused the re- duction rate to decrease with progressing process (Fig. 2). The kinetic, curve shows a clear minimum at about 25% reduction. The reduction then accelerates a little, only to sink to nil towards the end of the proces 11 Card 1/3 81701 Reduction of Manganese Ferrite by Hydrogen and 9/02o/60/132/05/28/069 Graphite B011/B126 0 Graphite completely reduces manganoferrite at 19000 ,The Spinell phase can only be proved for up to 2C% reduction. Possible phases here are ferrous oxide, manganous oxide, or their solid solutions. No metallic phase is detectable in this study. Above a 20% reduction there are two phases, the lower oxide and the metal phases. There are solid solutions of stable concentration here. According to the phase diagram of the Mn.-Fe sys-te&'., (Ref. 6)9 the solid y-solution is stable at 19'0000. X-ray pic- tures show a predominant quantity of the solid a-solutiong which is formed by cooling the y-solution. Admixtures of potassium- or sodium carbonateB accelerate the reduction of manganoferrits (Fig. 2). A phase with a Spinell-like lattice, similar to that of the ferrite used, is present in an 18.93% reduced sampleg but it cannot be proved at 28.9% reduction. A phase with an NaCl-like lattice (which corresponds to the sub-oxide phase of MnO), is present in all samples. Its lattice para- meter increases with the percentage of the reduction and approaches the size of the MnO-latticep without, however, reaching it (Fig. 3). On the basis of these data the authors give a reduction mechanism of manganese- ferrite: when the oxygen io removedg a surplus of metal ions is formed on the surface of the crystal lattice. They can either form a ferrite Card 2/3 81701 Reduction of Manganese Ferrite by Hydrogen and S/02Y60/132/05/28/069 Graphite B011 3126 lattice.or a metal phase. Which process predominates depends on the ratio of oxygen removal rate to the reaction diffusion. When hydrogen is used for the reduction, the oxygen removal rate is higher than that of the diffusion. When graphite is used for the reduction both rates are commensurable. The admixtures of alkali metal salts accelerate the chemical interaction of both the reducing compound and of that which is to be reduced. This is related to the variation in the electron con- dition of the lattice, into which univalent ions penetiate (Ref. 9). There are 3 figures and 9 references: 4 Soviet, 4 American, and I German. ASSOCIATION: Institut metallurgii Urallskogo filials. Akademii nauk SSSR (Institute of Metallurgy of the Ural Branch;of the Academy of Sciences, USSR) SUBMITTED: March 14, 1960 Card 3/3 "-/076/62/036/011/008/021 B101/B180 AUTHORS: Averbukh, B. D., Bra n n- 7-,.-Intonov, V. K.,and Chufarov, G. 1. verdlovsk) TITLE: Study of equilibrium conditions in the reduction of manganese ferrite by hydrogen PERIODICAL: Zhurnal fizicheskoy khimii, v. 36, no. 11, 1962, 9436 2441 TEXT: To find out the structure of ferrites and suitable conditions for their production, the reduction of manganese ferrite in hydrogen was studied at 9000C. Manganese ferrites of different compositions were produced by sintering Fe2 03 - MnO mixtures at '12000C in various atmospheres (CO ^r, CO + 0 or air), and by sintering Fe 0 MnO - Mn 0 mixtures. 2' 2 2' 2 3 3 4 Debye patterns showed that the resulting ferrites were single-phase. The .reduction was performed in a mixture of water vapor (P.20 . 4.579 mm Hg) and hydrogen (P. 10-3 - 102 mm. Hg).. After equilibrium had been established Card 1/4 S/076/62/036/011/008/021 Study of equilibrium conditions in... B100180 between ferrite and gas mixture, the water was frozen out, the p H measured, the degree of reduction determined from the H2 consumption, and p 02 the equilibrium pressure calculated. The phases formed in the reduced ferrite were identified by Debye patterns. Resultsi Except for those in air, which were higher due to oxidation, the ferrites sintered in different atmos- pheres showed approximately the same p H O/PH -values with the same degree 2 2 of reduction. Ferrites containing excess manganese owing to admixture of Mn3049 showed higher p 02 due to formation of Mn 304 -MnFe204 solid solu- tions. During the ferrite reduction, the lattice constant of the spinel phase gradually fell until it was roughly the same as for magnetite. At 10~4 reduction, a lower oxide phase appeared with an NaCI lattice, the constant of which increased as the-reduction proceeded. At 45% reduction, a metallic phase appeared, with the lattice constant of iron (2.a61 R). The reduction of manganese ferrite thus proceeds in two stagest (1) Re- duction to the lower oxide phase (Fe, Un)G via formation of non-ideal solid Card 2/4 S/076/62/036/011/008/021 Study of equilibrium conditions in... 3101/B180 solutions of YnFe 204and,Fe 504; (2) reduction of the lower oxide phase to iron. a tLe activities and Xthe activity. coefficients were calculated 41 &or the solid solutions (Table 3). There are 6 figures and 3 tables. The most important English-language reference i6s P. K. Foster a. A. J. E. Welch, Trans. Faraday Soc., 52, 1636, 1956. ASSOCIATION: ins-Litut metallurgii, Urallsk-iy filial Akademii nauk 55SR (Institute of Metallurgyl Ural Branch of the Academy of Sciences USSR) SUBMITTED% July 5, 1961 Card 3/4 BR,kYNINAj P.Z.;. AVERBUKH, B.D.; ZHtFUVLEVA, M.G.; CHUFAROV, G.I. Equ.ilibrium in the reduction of nanganese-zine ferrite by hydrogen. . Zhur.naorg.khim. 9-no.l.-23.0-231 Ja 164. (MIRA 17:2) 1. Drallskiy filial AN SSSR, Inistitut matellurgii. ,::ACCESSION NR: AP4042598 S/0076/64/038/007/1811/1815 '!AUTHOR:, Braynina, D. Z. (Sverdlovsk);'Averbukh, B. D. (Sverdlovsk). Chufarov,*'G. I. (Sverdlovsk). ,iTITLE: Equilibrium conditions in'the hydrogen reduction o f "manganese-zine ferrites SOURCE: Zhurnal fizi-cheskoy khimii, v. 38, no, 7, 1964, 1811-1815 -TOPIC TAGS: manganese ferrite, zinc ferrite, manganeAe zinc ferrite,: ferrite reduction, ferrite dissociation, ferrite crystal structure$ spinel structure, inverse spinel structure TABSTRACT:.. Equilibrium conditions at 700 to' 900C for the initial 06tages of hydrog4in reduction of manganese-zinc ferrites of varying :!composition are investigated. The equilibridm' constants wend idetermined experimentally and the equilibrium partial pressures of oxygen following dissociation of the ferrites were calculated. The 1:1attice constants were measured. It was shown that both the equilib i-rium partial pressure of oxygen and the lattice constants of manganese- ~;Izinc ferrites-depend in a nonlinear manner on the composition. It C.,d 1/2 ACCESSION NR: AP4042598 was found. that the dissociation' pressure'of,MnxZn1-xFe 04 i.ncre asea Fiat firs-t from the x value corresponding to zinc ferr te to a a maximum with a 70% zinc fe-rrite content, then drops to the x value for MnFQ204, The change in the constants of the crystal lattices of the solid solutions agrees with the Tact that manganese ferrite is inverted 'by about 20Z. Orig. art. has: 5 figures, 1 table, and 12 formulas. P ASSOCIATION: In 9 t i t u t me ta 11 u rg i i. (Institute lof. Metallurgy) SU13MITTED: llOct63 ENCL:- 00 SUB CODE: HH', SS NO REF SOV: 005 OTHER: 013 T 2 2. ....... BRAYNINA,-.R..Z.; 141-14 1 , A.N.; URIDAKOV, V.S.; GIIUFAROV, G. 1. Calculation of the "stabilization" energy of iron group ions in oxides having a spinel structure. Dohl. AN SSSR 160 no.2:379-382 Ja 165. (11-11IPJ, 18:2) 1. Institut metallurgii, Sverdlovsk. 2. Chlen-korrespondent AN SSSR (for Chufarov). 1 6 09 00 00 im phall- mom" nd It_ I"Ivid --A (am,. ca U7 ICi6 bpkA IM 30 Wb- with bvm in 010 -4H). 160-150, CL 00 HCI 91 tm, sa, (CHCLCH)Sla.21110- III ad tim of wMelt iiiith tIT' 00 j!~ords SON. rlwim..i~l.l =1 C"HAI, M.P. to ,3~ it V t room temp) a, ard C,H,51 0 p :jj!::l30* (d-MP') (mrcuri- 1. ;~Q ;Zts descAbed ab- P, IN ., tively a = evWviag COH at tcUl il: not TheL ffs"Y i0 C.11,%. sq. ac" "..t at of In oH at room temp, tjjtRATU~9 CLAUVOCAlION livibil A 13 It 0000 0 0. 00 0 0 0 0.0- 0 PA I I a tw o o 0 600 0090 AMA" .09 -40 .00 co 0 0411 goo Sao too _109 too 04 00 *0 00 90 90 00 so 13 13 3 00 Me"n of juyl ludoWetrides' with 2-thlorovinyl. mercury thlorlde.-Ii. M-WWU1"^nd It. Kb. Frvldlina. #kit. a4ad. scs. V.R-Y.S.. Cialse scs. ckim. 1047, 023-W (in Ruia6m).-Ileactions (d At ILI# with Ilam -CICII: C11. !IjCI were investigatod. Introdurtkni of a tic group Into the Ph ring facilitated thc exchange reaction, while intraduLtion of N03 sup1stswil it, as may be expected on tbc Iwis of clecteon displactivents caused by tbftc clec- tmnrepelling and clectron-attracting smps. The re- actions Of ph5nClj wilb CICII:CIIICI, and ICJI:CIiICl2 were Glut CX&Md.; in the Ist ilutatwe SnCL am Clul: - Clil-Ilict wcrc Immed (C.A. 40, MW), In the 2nd fit- *t~sacv the products vvere PUCI, CjIt. and SnCI4. This is explained by the +T effect for iodine being mallet thAn that Of Cl- PhIC12 (15 g-) WW 15 9- lranj-OC":- C11119CI (1) ill 40 tnl. 3~' , 110. shaken forseveral hrs. at room temp. until the KI lftt was neg., gave 9 j. (31%) pt. which, Iler w-Ashing with CIIC4,m. 133-4 andwas Identified &A ph(CjCfj:Cjj)jC7jjgC.j. m. 13-17' (frant dil. FtOlf). Treatment with lips, filtration, and evapa. ga%-v pjemyj(z.