SCIENTIFIC ABSTRACT VOLCHENKOV, A.I. - VOLCHKOV, A.V.

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December 31, 1967
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SCIENTIFIC ABSTRACT
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Manufacture of Sintered, Carbide Blanking Dies SOV/3673 carbide dies for blanldng stator plates and other elements of electrical equipment. Ito personalities are mentioned. There are 6 references: 5 Soviet and I German. TABLE OF CONTEM: From the Editor 2 Introduction 3 1. Typical Die Constructions 4 2. Metho -do of Mking Die Elements 26 3- Revats of the Use of Carbide Dies Under Production Conditions 63 4. Estimation ot the Economic Effect 64 Bibliography 67 AVAILABLE: Library of Congress wqpw/gap Card 2/2 7-7-60 VEDENEYEV, Nikolay Petrovich; VQjCjfl2UM,--Alskgnndr IvamVich; NOVGORCDOV, Aleksandr Stepanovich; ONIKUL, Ya.Ye., inzh.1 retsenzent; 17AYERAUB, D.A., kard. tekhn. nauk, red.; LEYMU, T.L., red. izd-va; SPEWSKAYA, OV., tekhn. red. [liard-alloy 13ngineering equipment; dies and press-molds) Werdosplaviiaia tekbnologicheskaia osnastka; shtempy i press- formy. Leningrad, Gos.nauchno-tekhn.izd-vo mashinostroit. lit-ry., 1961. 119 p. (MIRA 15:2) (Dies (Metalworking)) (Metalwork) VEDWEYEV, Nikolay Petrovich; V%q_ OV, Aleksandr Ivanovich; KcRsaov, Vaoiliy Dmitriyevich-016YOROMY; A16koandr Stepanovich; CIMMAKOVA, I.Z., inzh., red.; BILOGUROTA, I.A., takhn.red. [Hard-alloy blanking diaol Tvardosplavnye vyrubnr shtempy. Loningrad, 1960. 30 P. (Laningradakii dom naijohno-tekhniclioakoy propagandy. Obmen peredovym opytom no.18, Seriia: Kholodnais shtampovka, vyp.2). (KmA 14:1) (Punching machinery) VEDXNMV, Nikolay Petrovich; VOLCMIKOV, Aleksandr Ivanovich; KORSAKOV. Vasiliy Dmitriyevich; ACMXU)ZS, Sh.D., inzh., red.o. GVIVS, V.L.0 takhn.red. [Ptmehing dies reinforced with-hard alloys 6nd-~heiir manufacture) Vyrabnye shtampy, armirovannys tvardym splavom, i takhnologiia ikh 12gOtovleni 'is. Leningrad, Leningr.dom nauchno-takhn.propagandy, 1956. 65 P. (Informatsionno-takhnichaskii listok. no.28-31. Xlektricheskie metody obrabotki materialov). (MIRA 12:4) (Panching machinery) VOILHOKOV, A.R. (Rilga) Stencil on silk screen. Elek.1 tepl.tiaga no.7:33 -Tl '57. M-RA IC~:9' 1. Zaluestitell glinvno&;o takhnaloga Rizhakogo vagonostroitellnoeo zavods. (Riga-Stencil work) NOW,j LG.v kand, tddin. Q,.Uov IWho Stqigeotiono Ar changing the standard deoiCho fcr water pipDoo Tromp* otrol, 15 no*6o&3-45 Jo 165o i (14PA ill 122) MATVEYEV, K,V., karid. tekhn. nauk; MUROMDV, V.S., kand. tekhn. nauk; VOLCHENKOV,, G.Ya., inzh. Power damping and erosion in tailrace culverts. Trudy NUT no.176:34-52 163. (NIRA 17:6) BEGAM, L.G., kand.te-khn.nauk; VOLCHENKOV. G.Ya,, inzh.; NIKOLAI, K.V., Inzh. Using single! culverts vithout inlets. Transp. Otroi. 12 no.12:37-39 D 162. (KRA 16:1) (Culverts) TMESHCHKWO. I.7.; ~'= ILEV, V. V. Finding of Daurian hamsters, field nice, and weasels Bpontsneuosly infected with plague. Izv.lrk.goo.nauch.-Imal.protivochum.lust. 15:79-82 '57. (MIRA 13.7) (TUNGLIAO-RODENTIA-IDISIASES AND PICSTS) (PIAGUI) TFMMETSKAU, A.G.; BOCHMVAP G.jI.; VOLCHMOVA, V.A. Anisotropy of some p*sical properties of uacite. VestsHookoun. Ser.4: Geol. 17 no-5:44-49 S-0 162. (KIRA 15M) 1. Kafedra mineralogii Wakovsko universiteta. (Anisotropy) ~Coalcite) VOLCHKOVAP V.V. - . Automatio4o'r tekh. nauk 04 irrigation systems. Izv. AN Kir. SSR. Ser, eat, i no.8:117-124 162. (MIRA 16:6) (Automatic control) (Irrigatign) PANIKRATOV, X.D.;VOU:HMOVA, Ye.M. Irfect Of medicinal sleep on certain manifestations in experimental burns in dogs. Khirurgila, Moskva no. 12:12-18 Dec 1952. (CLML 23;3) 1. Of the Department of General Surgery (Director -- Prof. V. A. .B4tashov) and the Department of Pharmacology (Director -- Docent G. M. Sbpuga). Ivanovo Medical Institute. DARPACHRV. S.V.; SMIRNOY. M.V.; VOWHEIIKOVA, Z-S- ~ . I I - Adsorption of steam on mercury. Zhur.fiz.khim. 27 no.8:1228-1235 Ag '53. (MLRA 6:11) 1. Institut khimii i metallurgii Ural'skogo fil-'sla Akademii nauk SSSR, Sverdlovsk. (Adsorption) (Kercury) r"rR 17 _2V ee work &i atmosphere. of wate c n ! -njZ~ Chemical Abst. ,FM Khi 27 8 No. 6 Vol. 4 - , f . unction d fir in Ch, star. .25, r-Y HO llipin~'. The PA. Ix in v'rr'* aml Pt [" 11t0 va m 5- 1f)-$ air (ohe- c ~ l Mi 5 d l , 4tte v llf nt t p x t - 2 X 10 1 trita. IQ) is Irldep-mtknt of the varorptc.-um a["1 VC. /+ 2 - S J AUTJMR Smirnovq M.V. and Volchenkoval Z.B. 578 TIME: Equilibriini Potentials of Carbon-Dioxide Electrodes of Beryllium in Fused Chlorides. (Ravnovesnye Potentsialy Okisnou- golinykh Elektrodov Berilliya v Rasplavlennykh Xhloridakh.) PERIODICAL: "ZbUrnal Ne organ i cheskoZ Khimii" (Journal of Inorganic Chemistr V-0.L.I.Ey JN0.29 pp.417-42.L. kU,b.S'.R`.),qr7 ABSTRACT: From data in the literature the ef',df. of the cell BeO + C I Be'12 liquid I C121 C should be given by the formula 0-441 - 1'5 x 10-4 T. 0 0 Because of the very low conductivity of fused beryllium chlorid a direct measurement of er.df. could not be madev and for this reason the investigation described was limited to measuring the e,M',f. of cells with chlorine and carbon-dioxide electrodes of beryllium in fused equimolar mixtures of sodium and potassium chlorides, containing from 0'.064 to 7.35 wt'. % BeC12- It was found that the e'.m.f. of this cell changes witb temperature and mol.-fraction of beryllium ion concentration in the melt according to the empirical equation: 9 = (-0'.044 + 6.25 x 10"T - 0,992 x 10-4 Ft. [E e2+] 2 T log Fri - 0.992 x 10-4 T log fBe2+ f2Cl_ ) volts, where [W~ and Fcl-1 are the molar fractions, while fBe2+ and fel- are the 578 Equilibrium Potentials of Carbon-Dioxide Electrodes of Beryllium in Fused Chlorides.(Cont.) activity coefficients of beryllium and chlorine ions in the melt, Carbondioxide electrodes of beryllium were found to be reversible with respect to its ions in chloride melts. At low BeC12 concentrations the melts behave like ideal solutions. From the eiperimental data and those obtained in the literature the change in the isobaric potential on transition from pure liquid BeC14 to its dilute solutions in melted eutectic mix- ture of sodium chloride and potassium chloride was calculated to be 229400 - 39'.53 T cal'. per mol. BeCl Mixing the fused salts was found to be endothermic and to ?; accompanied by in- crease in entropy. There are ten references, two of them Russian. There are 2 Figures. Work was carried out at the Ural branch of the Academy of Sciences, U.S.S.Y., Electrochemical Laboratory. Received 29 October, 1956. Card 2/2 137-1958-2-2646 n" Tra'n'slatio~kqr-oom~:"Referatfliy zh Zral, Metallurgiya, 1958, N'r 2, p 63 (USSR) AUTHORS: Smirnov,M.V., Pallguyev,S.F., Volchenkova,Z.S. TITLE: The St-ate of the Oxygen in Salt Melts Containing Titanium (0 sostoy-anii kisloroda v solevykh rasplavakh soderzhashchikh titan) PERIODICAL: Izv. Vost. fil. AN SSSR, 1957, Nr 3, pp 94- 101 ABSTRACT: On the basis of experimental data on the electrolysis of fluoride/chloride melts containing Ti4+ it was shown that the effect of the atmospheric 02 within them and the suspended insoluble dioxid2 led to the formation of oxy-cations of the TiOZ + and Ti203 + type, which when discharged at the cathode yield well formed crystalline precipitates of the lowest Ti oxides. These oxide;s were precipitated with potentials 1.3 - 1.4 volts more posi- tive Vaan the potential used to segregate metallic Ti, and 2.2 - 2.3 volts more positive than the potential used to segregate an alkali metal. Tests were made to clarify the nature of the processes which take place at the cathode and at a carbon anode when electro- lysis occurs with small current densities. It was found that the Card 1/2 reduction of Ti4+ to the lowest valences at the cathode was 137-1958-2-2646 The State of the Oxygen in Salt Melts Containing Titanium accompanied by the disq~arge of oxy-cations with the formation of precipitates of the lowest Ti oxides. At the anode, simultaneously with the oxidation of the'lowe st -valence Ti, an electrochemical reaction took place with the oxy-cations adsorbed on the carbon: TiO 2 + + 1/2 C - 2 e = Ti 4+ (melt) + 1 /Z CO 2* Chlorination re- actions involving the particles of Ti02 -Ti203, and TiO suspended in the melt were also possible. The anode potential during these processes was r\j 0.4 volts more negative than the potential of a chlorine electrode. N - P. 1. Fluoride melts-Electrolysis 2. Chloride melts-In'lectrolysis 2. Oxygen-Determination Card Z/- A f i !I OrA) 6697/- . 6 00 (-/-1) SOV/81-59-13-45035 Translation from: Referativnyy zhurnal. Khimiya, 1959, Nr 13, p 44 (USSR) AUTHORS: Smirnov, M,V., Ivanovskiv, L.Ye., Pal'guyev, S.F., Volchenko -Z.S., Yushina. L,D. TITM: The emf-Methc)d for Study-Ing the Thermodynamics of Some Reactions at High Temperatures'~ PERIODICAL: Tr. In-ta khimii. Ural'skiy filial AS USSR, 1958, Nr 2, pp, 143 -151 ABSTRACT: In the electrolysis of fused chloride baths C02 is separated on the anodes prepared from an intimate mixture of oxides and carbon and the ions of the corresponding metals pass into the electrolyte. The oxide- carbon electrodes of thorium, calcium, beryllium, etc. in equilibrium are reversible in relation to their ions being in the electrolyte. This permits -to utilize them by the emf-method for elucidating the thermodynamics of reactions, in which oxides and carbon take part at high temperatures. The equilibrium potentials of the electrodes are determined by the activity of the Ions of the corresponding metals in the electrolyte and by the CO pressure over them according to the Card 1/2 electrode reaction M20n + n/29 - 2ne + (Aision) + n/2CO2, E 66974 SOV/81-59-13-45035 The emf-Method for StudyiN; the Thermodynamics of Some Reactions at High Temperatures const + (RT/n) FlnaMn + (RIV4F)ln'PC02. They do not depend on the molar ratio of CC and carbon. By measuring emf the changes can be found in the isobaric potential Z~~ Z' in the entalpy &H and entropy 6 S of the corresponding reactions of chlorination M20n + n/2C + nC12 = 2MCln (smelt) + n/2C02- Oxide-carbon electrodes in combinatIon with metal electrodes made it possible to study the thermodynamics of the interaction of the fused chlorides of thorium, beryllium and calcium with the chlorides of the alkali metals.- For determining the decomposition tension of the fused chlorides of higher valencies a method has been developed permitting to measure the value of the decomposition tension Of PlC12 and ThC14. The change in the thermodynamic parameterr; has been calculate for the reaction Th (solid) + 2C12 (gas) = ThC14 (liquid), & Z - 2.772 - 5.61, 10-~ T. Based on the emf of the cell Th I ThC12 11 KC1, ThC11 I Cl,3 C it has been found for the decomposition tension of ThC12; E - 3.27 - 10.9-10':4 T: & Z - 150,900 + 49.7T cal/mole. For the reaction ThC14 (liquid) + Th (solid) = - 2ThCl2 (liquid), a Z = - 23,000 + 23.8T cal/mole ThC12. The thermodynamics of the formation of alloys of thorium with zinc has been studied. For the reaction of re- ducing Th02 by carbon to metal A Z = 20,000 - 77.5T cal/mole. Card 2/2 A. Zolotarevskiy 67625 ~,67. J 0 (9j sy;/& -59-14 -~,,~~21 2 Translation from. Referatiimyy zhurnal, Khimiya, 1959, Nr 14, P 318 (USSR) AUTHORS: Pal,guyev, S.F., Volchenkovaj, Z.S. TITLE: The Problem of a Solid Electrolyte for Fuel Elements PERIODICAL: Tr. in-ta khimli. Ural'skiy fil. AS USSR, 1958, Nr 2, ~P 183 - 200 ABSTRACT: A method of preparation has been described and results are cited of measurements of the electric conductivity of solid electrolytes for fur;'- elements: a) O.K. Davtyan's eleotrolyte and its individual components (Na2C03, calcined monazite); b) a series of mixtures of oxides on the base of zirconium dioxide: 60 molar % ZrO2 + 40 molar % CeO2; 67.7 molar % Zr02 + 33.3 molar % La203; 3ZrO2 - 2CeO2 + 10 weight % CaO. Tbe measurements of electric conductivity were carried out by tne impedance- bridge method at a frequency.of 1,000 cycles. The circuit permitted the determination of the resistance with an accuracy of 1 - 10%, depending, on the value of the measured resistance. The conductivity was measured In a range of temperature from room temperature to 1,00000. 11ne activation Card 1/2 energies were calculated from the curve of the electric conductivity verz5,uS 67625 The Problem of a Solid Electrolyte for Fuel Elements sov/8i-59-14-50212 1/T (T is the absolute temperature) for sections with different slopes. On the basis of the obtained data assumptions are made concerning the character of the electric con- ductivity of oxide systems. There are 30 references. P. Lukovtsev Card 2/2 say/58-59-8-182-07 Translated from: Referati-tmyy Zhurnal Fizika, 1959, Nr 8. p 168 (USSR) AUTHORS.- Volchenkova, Z.3., Paliguyev, S.F. TITLE- The Temperature Dependence of the Electrical Conductivity of Nickel and Chromium Oxides PERIODICAL: Tr. In-ta khimli. Urallskly f1l.-AN SSSR, 1958, Nr 2, pp 201-207 ABSTRACT: The temperature denpendence of the electrical conductivity (d ) of polycrystalline samples of NiO and Cr 0 sintered at 1,5500C, was studied in the interval of 150 to 900 gC311 (Swas measured by means of the contact method with the aid of an alternating current bridge at a frequency of I kc. Contact resistances did not affect the temperature dependence of 6 . It was established that (5 for NiO, unlike Cr 203, in- creases sharply with an increase in the quantity of adsorbed oxygen, while the activation energy of the conductivity of NiO, measured on rectilinear sections, decreases. In the case of Cr2o the activation energy of 6 falls with an increase in temperature. & absence of Ionic conductivity under the conditions of the experiment was established by means of a chemical analysis of the areas near the electrodes. Card 1/1 E. Yenikeyev 05878 5(2) SOY/78-4-11-31/50 AUTHORS: Pal'guyev, S_ F,, Alyamoyskiy, S. I., Vo,lchenkova, Z. S,. TITLE: Investigetion of the Phasa Components of the System CeO -ZrO, 2 PERIODICALt Zhurnal neorganicheskoy khimii, 1959', Vol 4, Nr 11, pp 2571 - 2576 (USSR) ABSTRACT: This is a report on the structure and the ceramic properties of the s;fstem Ce02-ZrO The samples were prepared from mix- K tures of pure oxides. e spectroscopically determined content of impurities in the initial substances is given in table 1. The powders were pressed, a binding agent (natural rubber in benzene) being used for samples with more than 800/L Zr02. The samples-nere then sintered and X-ray investigated with copper K -radiation (powder camera of type RKD and inverting camera ~ _ shrinking o? type KROS). Besides, the density, color and linea' (Fig 2) in sintering were determined. Table 2 gives the che- mical composition, the phase composition, the lattice constants, and the color of the samples. A solid solution with cubic lattice develops between 0 and 50 mol% Zr02, a monoclinic phase exists between 0 and 10 mol% CeO a tetragonal phase l Card 1/2 lattice period changes at 70 m01% Zr02. Figure 1 shows that t~e C o5878 Investigation of the Phase Components of the System SOV/78-4-11-31/50 CeO 2-ZrO2 linearly with the COMDOSition and exhibits statistically distributed lattice defects which are probably situated in the lattice points occupied by the Ce4+- and 02--ions, The samples with 70 mOl% Zr02 have the greatest hardness; linear shrinking exhibits a minimum at 20-25 mol% ZrO ; the samples with 10-20 mold.' Zr02 are most intensely coloreq. A vigorous interaction between the two components seems to take place in this range (between 10 and 30 mol% Zr02). This interaction cannot be determined by X-ray investigation, it should, how- ever, become manifr.Az~t in the electric properties. There are 2 figures, 4 tablEs, and 3 references. ASSOCIATIONj Urallskiy filial AN SSSR.Institut elektrokhimii (Ural Branch of the AS USSR, Electrochemical Institute) SUBMITTED: June 5, 1958 Card 2/2 1b S163 BJJO~6000/001/013/014 Z4.710 D B1 U2 AUTHORS: Volchenkova, Z. S., Pal'guyev, S. F. TITLE: Electrical conductivity of solid oxide systems. II. The system ZrO 2 - CaO. Electrical conductivity and transfer number SOURCE: Elektrokhimiya rasplavlennykh solevykh i tverdykh elektrolitov, no. 1, 1960, 119 - 126 TEXT: The authors studied the temperature dependences of the conductivities of 100% ZrO 2 - 1006 CaO samples between 300 and 1000 0C, the transfer numbers, the structural properties of sintered samples and their ceramic ' 0 properties. Pure ZrO 2 and CaO or CaCO 3 were kept at 1200 C for 2 hrs. For samples with< 40 mole/i CaO the authorn uned CaO, for those with >40010 CaO, they used CaCO 3' The mixture (200 mesh grain size) was pressed to 1 0.1 0-062 - 0.4 cm tablets at -4000 kg/CM2 , and sintered for 1 hr at 1;00 - 20 C. Linear shrinkage during sintering, properties, and color were determined. G. V. Burov made X-ray structural analysis of the Card 1/4 316~~00 sl631160100 1/013/014 Electrical conductivity of solid ... B1IO/B1U2 specimens with Culla, radiation. At 15000C, solid solutions and fluorite- type crystal lattices formed with 10 mole% Cao. The primary solid solution (10.0 - 40.0 mole% CaO) yields good ceramics of high density, hardness, and stability in air. Free CaO contained in samples with 80.0 - 90.0 mole% CaO reacted with atmospheric humidity. The porosity and sample volume of zirconate formed according to ZrO2 + CaO ----,CaZrO3increases while its linear shrinkage decreases. The temperature dependences of conductivities measured with a-c bridges followed the equation x = A exp (-41/2kT) where is the conductivity, A and AE are constants. At 750 - 800 C, the curve showed a break (except for the range where solid solutions are formed). X-ray patterns of samples with>50 mole% CaO showed CaO lines. x was increased by the formation of Ca(OH )2 and CaO3and decreased by their decomposition (700 - 8000C). The rapid increase of x with the CaO contt-nt in the range of formation of solid solutions is probably due to an increase in oxygen vacancies in the lattice. With increased CaO content, the defects are no longer distributed statistically but systematically. The mobility of oxygen ions is thus reduced. With 15 mole% CaO, the conductivity maximum was observed at the minimum conductivity activation energyA E. The Card 2/4 31675 S/63 6C~000/001/013/014 Electrical conductivity of solid ... BIIOXB102 increase of linear shrinkage with the number of vacancies is probably due to the existence of oxygen vacancies only. CaZrO 3 had a x minimum and a AE maximum. The second, smaller x maximum at 60% CaO is probably due to the formation of the CaZrO - CaO eutectio. Another small x minimum was 3 observed at 90% Cao. The transfer number wAs determined from the weight losses. Three oxide plates 3 - 4 mm thick and 20 mm in diameter were used as catholyte, central piece, and anolyte Theyowere ground on each other, pressed between Pt electrodes, heated ;o 1000 C, and electrolyzed at 0.02 - 0.03.a for 2 - 4 hr. The transfer number was calculated as- follows: t - (Aa-1.19)/AB and t (Ak-1.19)/AB, where t and t are k a ' k a the transfer numbers of cation and anion, respectivelyoA a and 6k are the weight losses of anolyte and catholyte, respectively, A is the eleotro- chemical equivalent of the solid solution, B is the weight of Cu separated in a coulometer, and 1.19 is the electrochemical Cu equivalent. According to Table 2, t k was 4-0.01, ta was,,&E 1, Above 750 - 800 0C, ionic conductivity increases rapidly. In the range of Card 2/3 In 31676 S/631/60/000/001/014/014 Electrical conductivity of solid ... B110/BI02 the conductivity maximum, with 5 - 40 mole% Caot the samples can easily be sintered, are of great mechanical strength, low porosity, and 'nave no cracks. An increase in conductivity with increasing CaO content (4 5-10 mole';4,) in accompanied by increased linear shrinkage. The conductivity minimum caused by interaction of the components lies at 50 mole% CaO. Then, the conductivity increases and remains constant between 55 and 75 mole% CaO. These samples have good--ceramic properties and a weak color. The rapid decrease in conductivity at,100 mole% CaO (white samples with poor ceramic properties) is obviously caused by large amounts of non-reacting CaO and ThO The change in the conductivity activation energy corresponds exacti~ to the change of the conduction isotherms. There are 2 figures and 9 references: 7 Soviet and 2 non-Soviet. Card 3/3 - - -------- 29985-6 -Efflo OP(t)/EWP(b) Pr;-4#6.4 '(j)/EWT(a1)/EP F c rip(e) RWH/JD/JG ;--d ACCESSIO'N KR: ATOW678 S/2631/64/0001005/013310144 AMOR: Volchankova, Zo S.; Palthuyev, S. F. .-TITLE,*, The electrioal conductivity of solid oxides.- _IX. Mixtures of hafnium ox- 174de with the-oxides of bi!r ;Tamesluz, caUium stcontium and barr SOURCE: AN SSSP. Ural'skiy filial. Institut elektrokbimil. Trudy, no. 5, 1964. Elektrokhtmiya rasplavlesinykh solevykh i tverdykh elektrolitov (Electrcchem-Estyr of Jfused salt and solid electrolytes), 133-144 TOPIC TAGS: ozide conduct lid solution, hafnium oxide, beryllium oxide, tvtty, go magnesium oxide, calcium oxide, strontium crxide, barium oxide, ionic conduCT:ivity, electron conductivity ABSTRACT: Based on the aiethod of electromotive force in a cell with different par- tial pressures of oxygen around the electrodes the authors studied the nature of the conductivity of several samples of the nolil oxide systems 1"2-1~P-O, Hf(12-Mg(), HfO2-Cao, Hfo SrO and H1020BaO In a wide range of compositions and temperatures. The y showed Ra-t the concitc t i v i t v i t c oris i di-ra h ly g rea te r I n q vc- r ems whe rp - I id solutions of the substitLtion-deduction type (Hfo 2-M901 'f02-cao) form than in Cerd _7771- L 29985- 5 ~6 ACCESSION NR::, AT4040678 those systeras where there is no.formation-;ol! solid--solutions (11fO2 -Beo, RM. -Sro 0). -Measurements of,the linear shrinkage of the nample during cakin& and -it was -given - oxide- systems- werealso-~Ade-, and that the.-formation-of chemical compounds (CaHf0 GrRfO . and BaHf03) is 32 * accompanied by a minimum linear shrinkage in conductiPtIty. .~? high temperatures, the solid solytions, (Hf02-MgO, RfO2-CaO) are almost purely ionic conductors, while' the conductivity of, tho samples of the HfO2-Sr0 and HfO?-BaO systems is chiefly electron in nature. It increases as the partial oxygen pressure in the gas phase increases, i.e., it becomes hole-type. Moreover, this relationship is somewhat stronger in a system containing BaO than in a system with SrO. In the Hf02_8e0 system, neither a solid solution nor a chemical compound is formed, and the iater- action of the components Ls not reflected in the magnitude and nature of the con- ductivity. Orig. art. hais: 10 figures, 9 tables and I formula. ASSOCTMOR-. Inatitut elektrokh-imit, Urallskiy filial AN SSSR (Electrochemif~al institut_q_,,__qra1'ak branch, AN SSSR) SUBMITTED: 00 ENOL: 00 SUB CODE: IC. EX 1�6 Pw S"t :007, OTHER-1 002 cam PALIGUYEV, S.F.; VOLCHENKMi, Z.S. (Sverdlovsk) Electric ct)nductivity and transference numbers of the system CeO2 - ZrO;!. Zhur. fiz. khim. 34 no.2:452-455 F 6o. (MIRA 14:7) 1. Urallskiy institut elektrokhimii. (Cerium oxide) Mrc-)nium oxide) 9~, Ik4s, AUTHORS: Pallguyav, S. F., Karpachev, and Vol-2henkova, Z. S. TITLE: Transition From Electron to of the Composition of Solid PERIODICAL: Doklady Akademii nauk SSSR, PP. 11313-1141 8IL832 1-/020/60/134/00'J/020/023 B004/BO64 S. V , Neuimin, A, D, Ion Conductivity as a Function Solutions of Oxides 1960, Vol. 134, No. 5, TEXT: The authors wan'-,ed t study the influence of calcium oxide upon the electrical conduct4.vit ;~ f'solid solutions of cerium and zIrconium oxidg's-7-T. Tnce the Boli(F-so-lution 0.75CeO 2* 0.25ZrO2has the highest con- ductivity (Ref. 1), it was used as initial substance. CaO was added in varying amounts; addition of CaO of up to 40 mole% resulted in the formation of solid solutions. The preparation ef the samples was already described in Ref. 1. The relative electron and ion conductivities were determin8d by the 0solid electrolyte emf method at temperatures ranging from 500 to 1000 C, and herefrom the activation energy was computed. It was found that ion conductivity increases with an increase in tempera- Card 1/4 8h832 Transition From Electron to Ion Conductivity S/020/60/134/005/020/023 as a Function of the Composition of Solid B004/BO64 Solutions of Oxides ture, reaching a maximum at 750 CIC,, Only electron conductivity is found in the system CeO 2 - ZrO2; the addition of CaO diminishes the total ccn- ductivity with a minimum at approximately 6 mGle% CaO; the maximum is reached at 40 mole% CaOpwhm the conductivity is nearly 10e. ionic anj approximately equal to the electron conductivity of the Ce02 -- Zr02 system. The experiments were carried out with two electrolytic chains. a) (Pt)O Isolid electrolytel 02(Pt). The cell of this chain is schemati- pi P', cally shown In Fig. 1. The sampfe placed in a quartz tube between plati- num electrodes was at both ends in contact with oxygen of different atm). b) Met, Me' pressures (P1 = 1-0' P2 = 0.2 ~(O)j solid electrolytel JM,311(0), Me". This cell operated in vacuum without addition of gaseoun oxygen. The partial pressure of 0 was determined from the dissociation p:ressure of the oxides (mixtures of Fe and FeO, Cu and Cu2 0), and ranged from 10-7 tc 10"'25 atm. The electron and icn conductivities were determin- ed from E 6 + T0)1E0. E is the measured emf; te% to the avera,e Card 2/4 8h832 Transition From Electron to Ion Conductivity S/02o/6o/134/005/020/023 as a Function of the Composition of Solid B004,/BO64 Solutions of Oxides transference numbers of electrons and holes, reopectively. E0 the thermo. dynamic value of the emf: E0 = (RT/4F),In(p 21P1 ). Table 1 lists the ex- perimental data. Fig. 2 shows conductivity and AE at 1000 OC as a function of the CaO content. With rising CaO content in the system Ce02 - Zr02 - CaO, the authors found a steady transition from electron to ion conductivity. This effect was not observed in the systems CeO 2 -CaO ard ZrO 2 -CaO. The authors give the following explanation: 4+ 3+ As a result of partial reduction of Ce to Ce , first an intense ele.- tron conductivity occurs in the system Ce02 '- Zr02' Increasing addition ux of CaO inhibits this reduction more and more, and the ion conductivity caused by oxygen ions takes the place of electron conductivity, A decrease of conductivity in samples containing over 40 mole% CaO is attributed to the accumulation of free CaO not converted into a solid solution. There are 1 figure, 2 tables, and 9 references: 5 Soviet, 3 US, and 1 German. Card 3/4 Transition From Electron to Ion Conductivity as a Function of the Composition of Solid Solutions of Oxides ASSOCIATION: 8h832 S/020/60/134/005/020/023 B004/BO64 Instituf elektrokhimij Ura-l~skogo filiala Akadem;.i nFUK SSSR (Institute of Electrochemistry- (.,f the Ural Branch of the Acadeniv of lmc~iennea USSR) PRESENTED: June 6, 1960, by A. 11, Frumkin, Academician SUBMITTED: June 6, 1960 Card 4/4 4`( 5 1. , 1) 3 S/078/~2/007/003/011/019 B110[0138 AUTHORSt Pal'guyev, S. F., Volchenkova, Z. S. TITLEz Use of the electrical conductivity method to the study of the nature of interaction among the components of oxide mixtures PLRIODICAL: Zhurnal neorganicheskoy khimii, v. 7, no. 3, 1962, 615 - 617 TEXT: Using own earlier findings.(Zh. fiz. khimii, )A, 452 (196o); Tr. In-ta elektrokhimii Urallskogo filiala AN SSSR, vyp. 1, 119 (1960); ibid. vyp. 2; Dokl. AN SSSR, jJ4, 1138 (1960') the authors state that the con- ductivity method can be used to detect the formation of chemical com- pounds. Thus, for CaZr02, SrZrO,o 3aZrO,l SrCeO 31 and BaCeO 39 low minima'JI/ were found on the conductivity isotherms and on the curves of linear shi%inkage on sintering. It is suggest that the compound 2SrO-ZrO2 exists in the system Zr02-SrO, as alinear expansion of about 11~- occurs on sintering. Thermal and X-ray phase analyses of 2SrO-ZrO2 samples would be useful. In many oxide systems the dio3cides form cubic solid solutions of Card 1/3 S/078/62/007/003/011/019 Use of the electrical... B110/B138 the 8ec*ond kind with imperfect crystal lattice (vacancies in the anion sublattice). The number of vacancies grows with dioxide concentration. Conductivity grows with the number of vacancies until they react with one another. The conductivity peaks of ZrO 2-MgO; ZrO 2-CaO; CeO 2-MgO; CeO 2- CaO; CeO 2-SrO; CeO 2-ZrO 2- CaO with 15 - 25 molesl/:~ MeO are dependent on this. In the ZrO 2-MgO system besides the cubic, a monoclinicsolid-solution (0-4 moles~3~ MgO) was found by electrical conductivity. In ZrO -CaO, a 2 solid solution of monoclinic ZrO 2 was found with low CsO concentration. In ZrO 2-CeO 27 the electrical conductivity minimum is determined by the semiconductor properties of the oxides in the solid solution. In Ceo 2- ZrO 2- CaO, with 8 moles/a CaO, the minimum is related to the trarisi- tion from electron to ionic conductivity. The capacity for chemical interaction, reduction, and the type of phase are revealed as extreme values on the electrical conductivity - composition isotherms. Their interpretation, together with that of sintering shrinkage, can be used to reveal the very faintest physical properties of the oxides examined. Card 2/3 S/078/62/007/003/011/019 Use of the electrical ... B110/B138 V. It. Yeremenko (Zh. neorgan. khimii, 1., 2118 (1956)) is mentioned. There are 1 figure and 15 references: 12 Soviet and 3 non-Soviet. The two references to Engliah-language publications read as follows; W. B. Blumen- thal. The Chemical Behavior of Zirconium. D. van Nostrand Company Inc. Princeton, New Jersey, Toronto, New York, London, 1958, P- 1671 UOi, Hakadzava, Uetsuki. J. Ceram. Assoc. Japan, a, 139 (1956). ASSOCIATIONs Urallskiy filial AN SSSR Institut elektrokhimii (Ural Branch AS USSR, Institute of Electroohemistry) SUBMITTED: March 20, 1961 Card 3/3 0 nf- -Irj Z"'rX- /Z%WVn) + 13,o7i~~D al Ji -k - ~_7 S/2631/641000/005/1)16310166 ACCESSION NK., AT4048681 '-AU THOR Strekalovskly. V. N. _1srov-j_ G. V S marin 'V. A g j: TITLE:, Structural -,components of the hafnium oxide-calcium oxide syqtem~ S 0 IMCE r a I sk ty - f t I L a I I n it t L t u. t -'e I e k t rokh L-rati n a -ter dy *kh o. 5, 196.4: Elektro h rasplav enny*kh oolevy*kh i t elektroliLto,v-O;Iectrochomistry of -fused salt and solid electrolyter, 163-166 LTOP-1 TAGS:- -haf 6 lum- -a xi-de cal -cium oxideoxide ceramic, hafrAum oxide calcium oxide system, calcium hafnate, phase analysto ABSTRAM Experimental data on the phase composition of products of the high-temperature reaction between HfO.'and CaO have been (obtained to supplament the literature data. Compacted mixtures of HfOq~ with G-85 mol.;: CaO were sintered under various conditions, and the pro- ducts were analyzed by the x-ray diffraction method in an RKI) chamber 1-Card 1/.2 t~" v, */G w JDAG -5 C) ACCESSION NK: AT5007729 S/OOW/6310001000/0118/OL34- .-:.AUTHOR: -Pale gULIVY, S* F.*- lieuymin, A. D.; Vokhenkova. Z, Sa; Yushftm, L. D. 1944 T=: Electrictil conductivity of highly refracto 61des at high temperat-ires SOURCE: AN SSSR. Institut khimii 9ilikatcv. Silikaty i okisly v khimli vysc4cikh tcnperatur (Silicf-.tes and n)-'des irt 118-134 TOPIC TAGS: metal. oxide, refractory oxide, owide conductivtty, Thigh temperal:ure conductivity, rarE earth oxide ABSTRACT: The electrical conductivity of purl~oxfdas and their iDixr-ures as in- f - -_ - f vestigated. The pure oxides were (a) the dloxfdes of zirconiumflthori=11, ar4l' .er- ~1 i, , -in-- __. ium~JA(b) the oxides of beryllium, magnes calciumJ7 d strontiism- and (c) 1he oxides of vttriam. lanthanum. -nnd n e od vm f Lzm -7 1 r i a em ACCESSION NR: A15007729 corium dtowide KeOr)-R-o, C(~G,-Mgo, Cvo--Cao. Cc-0-,-.3rfj, Ce(-12-Rnfl), and (d) S-'stums r e L: t[IDS I rip, ''--a 1 .-OT '!'Ac't ~v -ir I:li;),)( vore o1 )"ted. The PXIPpr t-t I Z r 5 many r Ene 1" -)tner Pr.L,--rttos ~'--suh a -q "--Ai oy.-tem zv., 11-71-1176 0*1 '65, I"A "8 :9 InstItut o-'ek-trokhim.-.1 AN L%',-R. L-I rAcc AP6001304 SOURCE CODE: UR/036.3/6.5/001/008/1372,/137r) i.. V0, V. A. AUTHOR: Strekal2nmy, Ichenkova, Z. S.; SM __5 ORG- Institute of Electrochemistry. Ural Branch Academyg[Sci R clektrokbimii Ural'skogo filiala Akademii nauk SSSR) TITLE: Contrib.pti.an to the study of phase components in the Zr02-Pr0j.83 system SOURCE: AN BSSR. Izvestlya. Neorganicheskiye materialy, v. 1, no. 8, 1965, 1372-1375 TOPIC TAGS: zirconium compound, praseodymium compound ABSTRACT: The structural components of the Zr02-PrO1.83 system were studied in samples obtained by sintering powder mixtures of the two oxides. the phase composition of the producV was studied by x-ray diffraction and chemical analyses. In all samples, a phase with a fluorite structure was present. In mixtures of equimolar composition, another phase designated by X was also present. The reaction products behave differently toward hydrochloric acid: the solubility to low in the region adjacent to the original ZrO2, and high (almost complete) its PrOl. 83 is approached. The boundary of zero solubility Is the equimolar composition. The chemical compound X was insoluble In HC1. In comparing the x-ray and chemical analynes, the authors found It difficult to arrive at a general interpretation of the data: on the one hand, Card 1/2 - ____ UDQ 546.83116 L NRt Ke broad regions of solid solutionei with a fluorite-type structure were observed, the nature of the I formation of which varies; on the other hand, the characterof the distribution of the reacting ioxides is apparently related to the presence of a large number of phases in the reaction products. Orig. art. has: 2 figureo and 3 tables, SUB CODE: 07, 11 / SUBM DATE: 13M64 / ORIG REF: 004 OTH REF: 004 oidde DIP (e!-) /EW-1 W /"-;".1p (W )/ 1~~M-r .~Ylcj.z Xc Z: L;5022271 UR10363165100110071117111176 541.123.3 AUTHOR: Volchenkova, Z. S.; Strekalovskiy, V. N.; Pal1guyev, S. F. TITLE: Structure, electric conductivity, and nature of conductance in the ternary system (0.75CeO2 - O.25ZrO2) - CaO SOURCE: MI SSSR. Izvestiya. Neorganicheskiye materialy, v., 1, no. 7, 1965, 1171-1176 TOPIC TAGS: electric conductivity, cerium compound, zirconium-compound, cal- cium oxide ABSNACT: The structure and electric conductivity were inveBLigated in the system (0.75CeO2 - O.25ZrO2) - CaO over a wide range of compositio (from 0 1e, to 100 mole % CaO) and temperatures (500-1000C). The samples were rl repared by IN~ sintering powder mixtures for 2 hr at 1350C. X-ray phase analysis howed the -56- O.2.5ZrO2) with a I resence of t 6 phasea: solid solution of CaO in (0.1 e62 fluorite-ti rstructure, and CaO (at high contents of the latter). Electric conductiviOtIsotherms at 500, 600, 700, 800, 900, and 1000C were plotted.. The-7 ............ ~-~. - I c ange n the temperature coefficients of conductivity and the percent sbrinkage Isard 1/2 1;- 9286...-66 ACCESSION NR:. AP5022271 of the samples during sintering as a function of composition were determined. It is found that,as the amount of calcium oxide added increases, the unit cell constant of the solid solution changes. This phenomenon is correlated with the data on the total electrical conductivity and data obtained earlier from it determination of the transference numbers of ions 4nd electrons. OrLg. art. has: 6 figures and 2 tables. ASSOCIATION: 'Institut elektrokhimii Ural'skogo filiala-Akademii nauk SSSR (Institute of Electrochemistry, Ural Branch, Acade~z of Sciences SSS SUBMITTED: IOApr65 ENCT.: 00 SUB CODE: IC G-C NO REF SOV: 009 OTHER: 005 card 2/2 L 16608-65 -XM99MM MR: AT4048677 S/263 1/64/000/00-5/011-3/01.31 A0171011: Chebotin, V. N. ; V,Achenkova, Z. S.; PalIguyev, S. F. TITLE, Electronic conductivi 13' 4 1 j j 4 1 [tic crygLak in oquilibrium wtdi Oic gas phase. 111. Oxidation semiconductor ulth itdmixed accepEors SOURCE: AN SSSI1. Uraltgkiy filial. Institut alcktrolihimil. Trudy*, no. 5, 196-1. Elek-trokhimiya rasplavlcnny*Hi solevy*kh i tve-rdy*kh elektrolitov (Eloctrocliemistry of fused salt and solid electrolytes), 123-131 TOPIC TAGS: hafnium dioxido, ionic crystal conductivity, semiconductor impurity, oxygen pressure, solid electrolyte, oxidation semiconductor ------ABSTRACT:- Tlds-study was prompted, by the scarcity of -information on hafnium dioxide conductivity. It is a continuatiou, of two former communications by the same authors where they vvor~md out the system of equations which is,applied here to an ionic crystai. havingin addition to inherent defects, acceptors in the form of impurities. This theory is used to explain- the abnormttl dependence of the p-conductivity of hafnium dioxide on oxygen mre. 11b the-0 r is implaine in 19 eqaations and- the experimental procedures pre d ~--are described-.--hafaiumdioxide -with- Zr02(0. 75%_),.Si(6. 1%) __Ti(0W1%), 1%); Ni(