SCIENTIFIC ABSTRACT SHAROV, V.S. - SHAROVA, A.K.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001548620016-8
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: August 23, 2000
• Sequence Number: 16
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

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1-0

SHALROV, V. S.
25561 Skorost' dvizheniya kationov v sugongele gliny pri alektrolize. KolloidrVy 2,11a
Zhurnal, 19499 VYP. 4, S. 283-86
501 Letopis' Zhurma'rWkh Statey, Vol. As Moakvap 1949

~z " .11-1 .. .,
- - -- - -
25561. Skoroot' ;--ntdonov v z;us-7enilele fTliny -.)ri elektrolize. holloidnyy
L>
zhurnal, 1949, VYP- !,, -. 21586
SIO: Letuopis' Zh-arn-llultdh St,"eY, Vol. 34, ',',oskva, 1-049

, -V . o. -- -
255-01
Skorost' Drizheniya Katicnov v Suspengele Glirrl Fri llej,:trolize. Kolloidin-r .
19119. BYP. 11, s. 203 - 86
SO: IETOPIS INTO- 34

Cfl m !
owl
c
'Most
was deid. bY
into
~ooral, 30 saw 26 X
wo&vsccm)~ TwascWtV* % 6*-. and
10,41 per to t lot as
lar1=11; t 4 In a low
a I toy c M,
Cult.
&"allolm.

SHAROV, V.S.
Mechanism of the action of an electric current on a waterlogged
cohesive clay mass. Trudy NII &sn.i find.20-17:47-62 152.
Olay) (Drainage) (KLRA 9:9)

SHAROV, Vladimir Semenovich; DULIKIN, A.I., red.; BDRUNOVp N.L.,
(Superhigh frequency asynchronous motors] Sverkhvysoko-
skorostnye asinkhronnye elektrodvigateli. Moskva, Gos-
energoizdat, 1963. 287 p. (MIRA 16:7)
(Electric motors, Indqbtion)

79-2-2/58
AUTHDRS: Shchukarev., S. A.; Ybrozova,, M. P.; Kan Kho Tn.; Sharov,, V. T.
TITLF: The Enthalpy of Formation of Lithium and Barium Bismuthides
(Entallpiya obrazovaniya vismutidov litiya i bariya)
PERIODICAL: Zhurnal Cbshchey Khimii, 1957, Vol. 27, No. 21 pp. 290-293 (U.S.S.R.)
ABSTRACT: Lithium bismuthide (L3 Bi) was prepared by melting -the components,
taken in a stoichiom8tric ratio, in a hermetically sealed steel
crucible at a temperature of 12000. The compound obtained in such
a manner was a coarse-crystalline dark-greenish substance. The
enthalpy valve for this compound was fixed at - 39-5.10.5 kcal/g.
The barium bismathide (Ba3Bi2) was prepared by melting the bismuth
Card 1/2 with the barium, obtaimd by the high vacuum aluninothermy method,
in a steel crucible at a temperature of 21000. The enthalpy of

The Enthalpy of Formation of Lithium and Barium Bismuthides 79-2-2/58
formation of this latter compound was fixed at - 128.1 + 1.8 kcol/g.
The bismuthides of both metals appear to be quite typical intermetallic
compounds and the change in the heat of formation, resulting in the
displacement of magnesium by barium, is subject to entirely different
laws. The enthalpy values established were found to be different from
the values established by Kubaschewski and Villa (6).
2 tables, 1 graph. There are 11 references, of which 7 are S3,avic.
ASSOCIATION: The Leningrad State University
PRESENTED BY:
SUBMrTTED: March 24, 1956
AVAMUBIE: Library of Congress
Card 2/2

ACCESSION NR: AP4036534 S/0089/64/016/005/0456/0457
AUTHORS: Ganzha, V.D-~; Konoplev, K.A.; Trenin, V.D.; Sharov, V-T.
A
TITLE: Ion exchange installation for preparing reactor feed water
SOURCE: Atomnaya energiya, v. 16, no. 5, 1964t.456-457
a
1,.TOPIC TAGS: ion exchange water desalting, reactor water desal
ting,
kwater desaltings reactor feed water, water cooled reactor, moderated
i-reactor
ABSTRACT: The article describes an ion exchange water desalting
install'ation to provide water feud for water cooled and moderated
reactors. The installation has been designed at the Physical-
Technical Institute im. A.F. Ioffe, An SSSR as a substitute for an
unsatisfactory electric distillation-plant at the VVR-M reactor,
which has low capacity,"rapid scale forming; and low electrical re-
I'sistivity-of final product). The described installation produces 3
m3/hr feed water with 1 mg/l.salt, and less than 0.02 mg/1 chloride
i3ns. The water supply is adequate for a regeneration cycle of 50
m . Artesian water is used as feed for desalting (400 mdl.salts,
mostly Ca and Mg). Cation exchange resin KU-2 and anion exchange
Card 1/2

ACCESSION NR:.AP403
6534
resin EDE-10P were used with 250 Lswolle'n resin loaded into each
filter. Two airlift containers with 11 SO and NaOH provided for
regeneration. A diagram of the instaliation shows 4 filters, 2
regeneration containers and subsidiary equipment. Water control is
achieved by continuous measurement of specific electric resistivity
and intermittent chemical analyses. The installation has been in
operation since 1961. "The authors acknowledge B.P. Konstantinovts
suggestion to itch over to ion exchange desalting, D.M. Kaminker's
help in the op ration; P.P. Kory*stin's and I.V# Volf's help (All-
union Scientif*c Research Inst. of Hydrotechnical and Sanitary
Engineering) in laboratory tests and project recommendations." Orig.!
Jart. has: 1 figure and 1 table.
ASSOCIATION: None
ISUBMITTED: ogAug63 ENCLs 00
SUB CODE: IWAG Nx REF SOV: 000~ OTHER4 000
2/2
Card

L 25966-66 ___ i-rjT(--M)/Lvc(f)/EPF(n)-2/DIG(m)- --1JP(c)-- I.A.1
ACC NR% AP5026440 SOURCE CODE: UR/0089/65/019/004/0350/0354
AUTHOR: Ganzha-, V. D.; Yp D. M.*.
gorov, A. I.; Kaminker, Kolyadin,-A. B.~
Konglev, K. A,; qaykov, Yu. P.; Sharov, V, T.
ORG: 4649-
TITIZ: Blectrophoretic filter for reactor water purification
SOURCE: Atomnaya energiya, Y. 19, no. 4, 1965, 350-354
TOPIC TACS: nuclear reseapah reagtor nucle reactor meamm&dma, water
purification equipment
A&"#
ABSTRACT: In January, 1962, a formation of turbidity in the primary
loop of the VVR-M reactor of the Physicotechnioal Institute im. A. Fe
loffe, AN SSSR, was observed. In June, the turbidity was so strong that
a special electrophoretib filter for water purification was installed.
The turbid water contained a 54-potp-suspension of hydrate aluminum
oxide which was originated by the corrosion of aluminum reactor vessel
and fuel-element cans. A daily amount of about 2 g/Mw of suspended
particles was disobarged1into the water. The'installed filter was
equipped with the platinizqd titanium anodeplates, while the cathode
UM: 621.039*568

25966-66-
ACC NR, AP5026440
plates were made of 1 19 9T stainless steel. A cylindrical prototype of
the fill;er was experimentally tooted and the results were oxplained and
graphioally Illustrated. The tests showed that the chemici-il. compositioni
of turbid and filtered water was as follows:
Turbid Filtered
A1203 in m/kg 3.0 0
Fe +3 0.4 0.18
S102 6.0 1.3
02 0,96. 2.96
.optical density 0.065 0.008
The aelectod filter design data are silmmarized to-the following table:
Water flcw rate in kg/hr 250-500
Effective water flow in ou M/hr 0.5
Mectrode voltage in v i 110-220
Distance between electrodes in am 1
~
Contact time in min, (at 250 1/hr) 2
Total filter volume in liter 10.7
Interelectrode volume in liter 7.5
Eleotrode size. in mm 170x572
Number of anode plates 4
Number-of cathode plates 5
Filter dimensions in nm 400x;!24xM

L 2~966-66
AM NR, AP5026440
The filter-has a small hydraulic resistance and needs only about 0.5 k-.11
for its operation. A flow diagram represents schematically the ciraula-'
tion of water in the primary loop of the reactor. AnotherTi8ure shows
a photo of the electrophoretic filter which was succe-ssfully used for
purifyine water in the VVR-M reactor. The authors express 'their Grati-
tude to Academician B. P. Konstantin_qff_for his continuous'Interest.
Expressioni,of thanks are also given to V. P. Rodzevich (for apparatus
design) I *V. D. Trenin and R. N. Rodionov7?-o-r--a--n-a-lYs-fs-l-and to D.-A.
Yashin anC . a. - REFZ-Ov Orig. art. bas: table-6
ond 6 figures.
SUB CODE: 19,13 / SUBM DATE: 4-Tuly64 /. ORIG RU:001. 0TH -RF-F,',0M
cord 3/3

8/081J61/000/019/068/085
AUTHORSs Ifekhtiyev, S. D....SharoT, V,-Y-, Pasharev, T. A.
TITLF,s-':' Calorific value of some aromatic cyclohexyl and dicyqlohexyl
hydrocarbons
PERIODICA,Ls Referativnyy zhurnal. Khimiya, no. 19, 1961 424, abstract
19N182 (Azerb. neft. kh-vo, no. 2, 1961, 40-~2)
TEXT.s Data are given concerning the calorific value of aromatic cyolohexyl
and dioyolohexyl bydrocarbons~per weight and volume. These data were
.calculated starting from molar combustion heats and molar Ikydrocarbon
volumes aocording to the method developed by V. M. Tatevskiy. ~bstracterls
notes Complete tranelatiO4
.Card 1/1

MEMITIYEV, S.D.; ALIYEV, A.F.; YMMAROV, Yu.G.- SHAROV, V-V-
Z)ernal decomposition of cyc'o~exane under conditions of extra
rapid pyrolysis. Azerb.khim.zhur. no-3:3-13 '-159- (YJ-R,, 14: c,
(Cyclobexane) (F~rolysis)

SOLOMMKO, H.S.; CIMIKOVSKLY, V.S., redaktor; SUROV, Ta.l., redaktor.
[structural mechanics of the ship]-Stroitel'naia makhanika korablia.
Pod obshchel red. IA.F.Siarova. Leningrad, Gos. nauchrio-takhn. 12d-vo
mashinostroit. i sudostroit. lit-ry, Laningradekoe otd-nie. 1954.
415 p. ~W""Ah 8;1)
(Shipbuilding)

NOVOZHIIAN. Y.T.; qz~, Ya.]F.. redaktor; CHICMUNOVA, V.S., redaktor;
FRUMN, F.S., tommNOT70me y rodaktor
[Theory of thin shells] Teoriia tonkikb obolochek. [Moskva] Goo.
izd-vo sydoetroitellnoi lit-ry, 1955. 344 p. (MLU 8:10)
(Blastic plates and shells)

SHAROV, Ys.T.,knnd.tek-hn.nauk
Impact of waves on ship bottoms. Sudostroenle 24 no.4;5-9 Ap '58.
(Ships--Hydrodynamic impact) (MIRA 11:4)

SEAROV, Ya.F., kand.tekhn.wu
----------------------------
Impact of ship hull bottoms agaient oncomin vaves. Trudy NTO sud.
prom. no.35:29-38 160o fMIRA 132-9)
(Ships-Hydrodynamics)

1. s=v,' Ya. V.
2. IJO'"M (600)
4. Chemistry - Study and Teaching
7. Extracurricular activities, Khim. v shkole, No. 5, 1952.
9. Monthly List of Russian -Accessions, Library of Congress, February -1953. Unclassified.

KCKAROVSKIY, A.N.., doktor tekhn, naukq prof.; SHMVA) Ye.A., red*;
YEZHOVA, L.L., tekhn. red. -
(Structural design of accelerators) Stroltellmye kcnetraktsil
uskoritelei-, lzd.2,-, perer-. Moskva# GOS. izd-vo "Vyoshaia
shkolay" 1961. 133 p. (MIRA 15:3)
(Particle accelerators)

ACC NRI AP607,5928 -SOURCE CODEs Ult/U4-13/66
AUTHOR: Arinuchidn, L ' S., Dumov, V. I./ Xnyshev, V. A. Moskovskiy,
V. D./,Polinovaidy, A. Yu./ Pharov, Yu. A.
10RG: none
TITLE: Pump unit for two-eircuit fuel systems for power planto
SOMICE: Izobreteniya, promyshlonnyye obraztsy, tovarnyye znaki, no.20,
'1966, 19j;
1 a :_
TOPIC TAGS: pump.Muel system, fag ;n!ryi44=_z9%0 1.9=9=~_,ruei feed system,
1UNGRA VV "'~OT_hbrllpropoacd pump un1t conflicts of a pump with a low pre surej
,circuit and a pump with a high prounuro circuit. To 1mProve Jtgl
ificicney and to decrease the nyoteml a size and woight, the imptillart)
lof both pumps are mounted on a common shaft and an annular collector in
!positioned between the impellers; the-collector Is connected by ducta-...I---
It-3 the low pressure pump putlet duct and to the high preasure pump
'Inlet cavity. In order-to improve the anticavitional characteristics
of the unit, a vajh~aiio'n of this unit Is made so that the ruel bv-Dann
from the high pressure circuit rbno through a duet-wh1ch is posiftoned
tangentially to an annular chamber located at the unit Inlet. (see.
Fig.1).
Card 1/2 F~i;

NRA
Orig. art. hans I figure.
suB coDE: 21/ suBm DATz: o5oct63/
Fig. 1. Pump unit
I- Impeller; 2- drive
shaft; 3- annular col-
lector; 4- ducts; 5- low
reanure pump outlet duct;
9
- high pressure pump in-
let cavity; 7- high pres-
sure circuit; 8- tangenti-
ally positioned duct; 9-
annular chamberl 10- unit
inlet
[WA-883

SOV/120-58-4-12/30
AUTHG1ZS:Bartenev,L. S.1 Glebovichl G. V., Gox7achev, L. V,)
TITLE: A. High-Speed Pulse Oscillograph (Impul'snyy skorostnoy
ostsillograf)
PERIODICAL: Fribory i tekhnilca eksperimenta, 1958, Nr 4, pp
(USSR)
ABSTRACT: An oscillograph with deflection plates of transaissio_-
line type is described; two time-base systens are
the faster of which gives one complete syjee-,) i-a ~~.).xat
4, x in-9 9ec, There are two oscillators, a'200 Mcls m4 a 500 Mo/s
osclllator. T atrons are used to develop -tne sweep,
.hyr
ages? and advantao-e is taken of their ionization characteri_~--
Cj
tics to get really fast response. Post-deflection
ion (3 Iff) is used; the vertical deflection system has a
pass-band extending up to 1000 Mc/s. The deflection sensl-
0 -
tivity is 9 V/iaa. Ex-amples of oscillo-rams taken a.re
Caird 1/2

SOV/120-58-4-12/30
A.High-Speed Pulse 0scillograph
presented. The paper contains 4 figures and 2 references,
of which 1 is Soviet and 1 English.
ASSOCIATION: -Nauchno-issledovatellskiy radiofizicheskiy institut
(Radlophysics Scientific-Rezearch Institute)
SUBMIMM: October 24, 1957.
Card 2/2

KOTENKO, L.P.; KUZNETSOV, Ye.P.; MOWN, G.I.; SHAROV, Yu.B.
Elastic scattering of 2.8 Bev./c:F--mesons on hydrogen. Zhur.
ekap. i teor. fiz. 42 no.5:1158-1165 W 162. (KM -15:9)
1. Fizicheskiy institut imeni P.N.Lebedeva AN SSSR-
(Mesons-Scattering) (Hydrogen)

ACC NR, Ap7001460 (A~ SOURCE CODE: UR/OW316-6/000/02110211/0212
S:;
INVENTOR:- Arinushkin, L.
Dumov, V. I.; Luchkin, S. M.; Polinovskiy, A. Yu.;
Sharov. Yu. A.
ORG: none
TITLE: Self-priming centrifugal-pump assembly. Class 59, No. 188308
SOURCE: Izobreteniya, promyshlennyye obraztsy, tovarnyye zaaki, no. 21, 1966, 211-212
TOPIC TAGS: aircraft fuel pump, axial pump, fluid pump, centrifugal pump, engine
fuel pump
ABSTRAM This Author Certificaee introduces a self-priming centrifuge Pump for
fuel systems such as those used -in aircraft. A common casing contains a main
centrifugal pump and an auxiliary fluid-flow ring pump. The discharge cavity of the
latter connects with the fuel tank. The intake chamber of the fluid-flow ring
pump is connected to the forechamber of the main pump rotor by means of a channel
which'encircles, for instance, the hub of the main rotor, and another channel in the
casting connects the functional chamber of the ring pump to the discharge cavity
of the mi%in- pump. This arrangement improves the anticavitational properties.of the
Card 112 -112

-ACC NRt AP-j
7C
Fig. 1. Self-priming centrifugal pump
1 - Intake chamber; 2 - rotor; 3 - channel; 4 rotor
hub; 5 - functional. %.chauber; 6 -,discharge cavity of
j~ the main pump.
astembly and reswIts in wre dependable operation. In another version of the above
assembly the main pump includes an engaged axial rotor, and in this 'case the intake
of the ring pump is also connected to the forechamber of the axial rotor (see Fig, 1).
Orig. art. has: 1 figure. [SAI
SUB CODE: 13, Ol/ SUBM DATE: 30Dec62/,ATD PRESS: 5110
Card 2/2

L 22h93-% AFWL/AEDC(a'I/ASD(f)-3/AAMC
ACC-73310'al.' NR; AP5002420 S/b286/64/WO/bU/0O24/0O24
AUMOPS: Dobrovol'skiy, V. L.,- Kaspruk, Yu. V.; Fqabov, B. I.; Sharov,-Yu. N.;
Mildmylina, S. "I.; I7anov, Yu. V.; Budrik, G. V
T!"LE: A method of raising and holding a cassate, vith a source of ionizing
radiatiQn, in a vertical pipe in a suspended state. Class 21, No. 1669?5
a"ACE; �yji4eten' izobreteniy i tovarnykh znnakov, no. 24, 1964, 24
ABSTRACT: This Author Certificate presents 4,_-meith6&~of acpp3,ying the dynamic
pressure of a liquid or gas current to raise and hold a caseets, with a source
of ionizing radiation, in a vertical pipe in a suspended stste.
ASSOCIATIONt none
SUBMWED: MovQ
ENCL: 00
-ME.-, NO REF SOV: 000 OTHER: 000

SHMov yuriy Vladimirovich; BASOV, ym.T.,, redaktor; RYBIN. I.V.,
"fe-ftnichaskly radaktor
Cjktracurricular work in engineering; a practinal m&UuAl for teacbers,
Pioneer leaders, and workers directing the work of young engineers)
Vneklasensia'rabota po tokhniko; metodlebaskoe posobte dlia uchitelai,
p-ionervoshatykh I vueshkollufth rabotnikov. vedushchikh rabotu. s
Lunpli tekhnikami, Moskva, Goes uchabno-podagog. isd-vo Ministerstva
prosveshchenita MSARO 19,55.- 203 p. (HIM 9 '. 12).
(Inginearing-6;tudy and teaching)

CHURIN, V.; SHAROVA, A., DAVIDOVICH, V.
'r . I
he now equipment and industrIal ITyglone. Sov.profool-my .- 7
. no.10:18-21 W 159. Nak 1219)
(Industrial hygiene)

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Indiiiiia. pMm and PfMMIuM 10 th,0 IM-44101ts and
the wage FW"U Ofaw Dedeffous mwujv of Una.
FMIN)v Metal.
V. S. syrokomsicil and A. K. Sharovs. 7'
No. 11, ZI-7; KAIWIW~i' 2, No. 3,%3-4
(Igno).-Them were fatutif in the intermediate and.the
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1. DEKMV, N. V.. SgaoVA, A, L.. POLYAKOTA, V. M.
2. Tim (6oo)
4,, Oulf ate s
7. Reaction of titanium sulfate with Potassium sulfate.
Doki. AN SSSR 87 No. 5, 1952
9. Konthly Lists of Russian Accessional, Library of Congress, K_a_r_t-h_ 1953. Unclassified.

t)
Chemistry - I'liermodynardes. ghe.rmochemistry. B-8
USSR/Physical
. Equilibrium.. Mysicochumical, Analysis, Phase Transitions
Abs Jour : Referat Zhur - Khimiya, No-2, 1957, 3747
Author : Chukhlantsev V.G.., Sharova A,K.
Inst : Kiev State University
Title : Solubility Products of Uranyl Arsonates
Orig Pub : Zh. neorgan. khimii, 1956, 1, xo 1, 36-41,
Abstract By the isothermal method at 2& vere secured data on the
solubility of uranyl ars,,=tes UOpMA-sO4 -.
M = H, N94, K,
.
Li and Na) in dilute solirtious of nitric and sulfuric
acid. 'By utilizing previously derived equations i 'Babkc
"IU, 1935, 4) determinatioa was
A.K,, Naukovi. zapiski K,
made of the solubilit rod
ts of the arsenates under
Y
stUA 7
T
~y'L U02 -7 ZM _7, Vnich are (at 20P):
I.
2
1.71 10-24 (M Nffk 2.52 10-23 (m x); 1.35

Car& 1/2- -.92

d-li -k t-, Y 4-
587
AUTHORS: Demenev, N. V., Milyutina, M.I., Sharova, A. K. and Shtin',A.P.-
TITLE: Preparation of an Acid Sulphate of Trivalent Titanium.
(0 poluchenii kisloy sernokisloy soli trekhvalentnogo titana).
PERIODICAL: "Zhurnal Neorganicheskoy Xhimii" (Journal of Inorganic Chemistr
Vol.II, No.2, pp.465-467 (U.S.S.R.)-Iqf~
ABSTRACT: The formation of a violet-coloured crystalline precipitate
in quantities strongly dependent on sulphuric-acid
concentration was observed when working with reduced acid
solutions of titanium. To determine the composition of the
precipitate and elucidate the conditions leading to its
formation was the object of the work described. The solutions
used contained either 15.25, 25.0 or 37.5 g/litre of TiO
i
initially, and the final contents of this and of sulphur
c
acid were determined. The results are tabulated and indicate
that with 700 - 100 g/litre of H SO precipitation occurs to
90-97%. Analysis of the salt pKp&d with careful
exclusion of oxidation gave the composition Ti (SO H so .8H C
~4 2 4 2
i
1u
It is a crystalline powder soluble in water, d
sulphuric and hydrochloric and concentrated sulphuric acids.
It is recommended as a source of trivalent titanium for
analyAical work. There are three references, one of which
is Russian. 1 Table.
Received April 26, 1956.
Card 1/1

S/137/60/00()/006AO1/015
A006/AOO1
Translation from: Referati-nyy zhurnal, Metallurgiya, 1960, No. 6, p. 70, # 1223(
AUTHOR: Sharova, A.K.
T=: Studies of the Chemistry and Technology of Rare Elements
PERIODICAL: V sb.: Uchenyye Urala v bor'be za tekhn. progress, I. Sverdlovsk,
1959, pp. 137-146
TEXT: Studies are listed, carried out at the laboratory of rare elements
at the Ural Branch of AS USSR, on the chemistry and technology of rare elements.
There are 19 bibliographical titles.
G.S.
Translator's note- This is the full translation of the original Russian abstract.
Card 1/1

SHARMA, A.K.-, FOTIYZV, A.A.
Production of titantui-n dioxide from the product of the sodium
sulfate reduction synalting of an 11TIenite conenntrate. Izv.Sib.
otcl.All SSSR no.4:52-63 159. WIRA, 12:10)
1. Ural'skly filial Akadenii nauk SSSR.
(Ilynenite) (Bodiuvq sulfate) (Titanium oxides)

SHMVA. A 0 CEMFAROVA, I.G.; VITTIKH, M.V.; SHDSTAK, F.T.
Recover7 of germanium from dilute solutions by an ion exchange method.
Izv. Sib. otd. AN SSSR no.8:36-42 159. (KIRA 13:2)
I.Ural I nki)r filial AN SSSR.
(Germantu*--Analrels) (Ion exchange)

SHAROVA, A.L;SHTIN, A.P.
Rioblum phosphates. Izv. Sib. otd. AN SSSR no.9:40-47 159 NIBA 13-3)
1. Ural'sk'y filial AN SSSR.
(Nibbium phosphates)

SHTIN, A.P.; 9HAROVA, A.K.
Tantalum phosphate. Report 36.2. Izv.SIbqotd.AN SSSR no.10:
87-94 '59. (MIU 13:4)
1. Ural'skly filial Sibirskogo otdeleniya AN SSSR.
(Tantalum phosphate)

S/598/60/000/004/010/020
D217/D302
AUTHORS: Sh v A.K-- Demenev, N.V., Fotiyev, A.A. and
Ivakin, A.A.
TITLE: Production of titanium dioxide from ilmenite concentrates
by sodium sulphate melting
SOURCE: Akademiya nauk SSSR. Institut metallurgii. Titan i yego
splavy. No. 4. Moscow, 1960. Metallurgiya. titana, 95-101
TEXT: In all experiments, ilmenite concentrate from the Irshinsk depo-
sits, of 0.056 mm mesh size were used. The chemical composition of the
concentrate was as follows: 51.46% TiO 2, 33.78% Fe, 1.04% Al203, 1.56%
Sio 21 0.86% MgO, 0.26% V2051 0942% MnO and traces of CaO. Wood charcoal
with an ash content of approximately 2% and 0.4 mm mesh size was used as
the reducing agent. The main reagent, Na 2s0 4' is a natural producto
The charges of ilmenite concentrate, Na 2 so4and wood charcoal were
Card IA

S/598/60/000/004/010/020
Production of titanium ... D217/D302
thoroughly mixed and transferred to porcelain or graphite crucibles.
Charges weighing 200-300 gram were used for the experiments. The mix-
tures were melted in a silite furnace. It was assumed that the melting
was complete at the moment when gases ceased to be evolved from the melt.
Each crucible was then withdrawn from the furnace and the melt cast in
a graphite mould. After cooling, the melt was ground and subjected to
leaching with water and acid* The residue was calcined and analyzed,
for its iron and titanium dioxide content, When ilmenite concentrates
are melted with Na 2S04, the following reaction occurs: FeTiO 3 + Na2so 4+
2C = FeS + Na_'TiO3 + 2C02 0 The reaction intensity depends among other
factors on the method of melting and the surface area of contact of the
various phases. In order to find the conditions under which maximum
extraction of iron in aqueous leaching is attained, the following factors
were studied: Volume ratio between solid and liquidg time of stirring,
temperature of leaching and degree of grinding of the melts. In all
experiments, leaching was carried out at 25 0C for 15 minutes. The
Card 2/4

S/598/60/000/004/010/020
Production of titanium D217/D302
particle size of the melt was 1.6-0.85 mm.. It was found that complete
extraction of iron from the melt can be attained only when the sodium
sulphate and carbon contents in the charge are sufficiently high., The
optimum ratio between concentrate, sodium sulphate and wood charcoal
in the charge (in parts-by-weight) is 1:2:0.6. At 1000-1050 0C, complete
decomposition of the ilmenite concentrate0occurs (up to 98 or 99%).
No melting of the charge occurs up to 900 C. At higher temperatures,
intense melting occurs with much evolution of gas and a homogeneous
fluid melt is formed. Extraction of iron sulphide into the solution
depends on the time of leaching and the degree of grinding of the melt.
An increase in the time of leaching from 15 to 60-90 minutes decreases
the amount of iron extracted into the solution owing to the transforma-
tion of the sulphide from a soluble form into a gel. The optimum condi-
tions for extracting iron sulphide in the aqueous solution (up to 80 or
85%) are as follows; ratio solid: liquid = 1:10, solution temperature -
0
70-80 C, degree of comminution of the melt = 2-3 mm and timeof leaching
= 15-20 minutes.. As a result of treating the residue, titanium dioxide
Card 3/4

S/598/60/000/004/010/020
Production of titanium oo. D217/D302
is obtained in a form suitable for metallurgical purposes and for pro-
ducing titanium tetrachloride. There are 5 figures, I table and 9
references*, 6 Soviet-bloc and 3 non-Soviet.-bloc. The reference to the
English--language publication reads as followag J.C. Witt, Am. Chem. Soc..
43, no. 4, 734, 1921.
Card 4/4

SHOSTAK, T.T.; VITTMEL N.V.; SUROVA, A.K.; OWAROVA, I.G.
Separation of geresulux b7 an ion exchange method, Izir.Sib-otd.
AjF sm no.a.-69-74 160. (XIRA 13: 9)
1. Nizhne-Tagillskoye otdelsnly4~ lauchno-iseledavatellskogo
inatituta plasticheskikh mass I Urallskly filial AN S33B.
(Germsaium) (Ion exe,hange)

S/828/62/000/000/009/017
E039/E420
AUTHORS: Shtin, A.P., Sharova, A.11.
TITLE; Investigation of the physico-chemical properties of
phosphoric acid compounds of niobium and tantalum and
their separation
SOURCE: Razdeleniye blizkikh po svoystvam redkikh inetallov.
Mezhvuz. konfer. po metodam razdel. blizk.ikh po svoyst.
red. metallov. Moscow, Metallurgizdat, 1.962, 107-115
TEXT: Complexes of Ti.-Nb-Ta usually contain phosphorus. In
order to determine the effect of phosphorus on the behaviour of
these metals the properties of the phosphbric acid compounds of
Nb and Ta were investi.-ated. Nb and Ta precipitated from solution
in sulphuric acid by the action of phosphate ioas can be presented
in the form: 2Me2O5-P2O5.6H20 (where Me is Nb or Ta). The
dehydration of these phosphates is shown to be a gradual process
,largely complete at 5000C. However, X-ray diffraction analysis
shows that at 8000C in the case of niobium phosphate the
composition can be represented by 02Nb2O5*P205,O.85H2O and in the
case of tantalum phosphate at 900 C the corresponding formula is
Card 1/2

5/828/62/000/000/CO9/017
Investigation of the phyalco-chemical .. E039/E42o
2Ta205'P205-0.81H20; in addition the transition from the
amorphous to the crystalline state is observed on dehydration.
The dehydrated salts have a higher density than the hydrated
salts. The conditions for separating Nb and Ta in the H2SO4
solution by the Pphosphat,01 niethod,,2;1~i- -.'s-i4diied. Precipitation of
tantalum phosphate from a solution containing 850 to 1000 S/litre
Of H2SO4 gives a separation of Ta from Nb of 90 to 95"'0. With a
high Nb content in the solution (Ta20g:Nb20 5 = 1:25) the product
has a higher N1b concentration (i.e.-N 205:Ta205 = 1:2). When
the ratio of Nb2o5:Ta2o5 = 3:1 and 1:1.8. the ratio of
Ta20 :Nb205 in the product is 8:1 a-nd 14:1 respectively. After
treaLent. with an alkali the phosphate precipitate contains more
than 90% Ta205, Repeated precipitation is recommended only from
solutions with a high Nb content. There are 4 figures and
6 tables.
Card 2/2

5/828/62/000/000/010/017
E039/E42o
AUTHORS: Sharova, A.K.A-Demenev, N.V., Polyakova, V.M.,
-71-ilyutina, N.I.
TITLE: The physico-chemical basis of methods of saparazing
titanium and the earth acids .
SOURCE: 11azdeleniye blizkikh po svoystvam redkilch metallov.
,%Iezhvuz. konfer. p6 metodam razdel. blizkikh po svoyst.
red. metallov. Moscow, Metallurgizdat, 1962, n6-123
TEXT: This work was undertaken because the properties of the
fluoride complexes of Ti and Nb and their solubilities in various
mineral acids are of importance in the development of separation
processes. It is shown that the optimum.conditions for the
separation of Ti and Nb from H2504 solution are: 107/9 11i2SO4,
154' HF and 10%. KCI. From a study of the interaction of potassium
salts with Te and Nb in H2S04 a method is developed for separating
Ahese elements from medium and strong acid solutions. This
separation depends on the principal valency change in Ti. Vhen
a potassium salt is introduced in H2SO4 solution containing Ti
(180 to 250 g/litre H2304) the double sulphate of Ti and K is
Card 1/2

S/828/62/000/000/010/017
The physico-chemical basis ... E039/E420
precipitated. When Ti and Nb are present in solution both metals
are precipitated in the form of isomorphous compounds. However,
if Ti is present in the trivalent form, it is not precipitated and
the Nb is separated from it in-the pre.cipitate in the form:
the solubilities of
K2S04(NbO)2(SO4)--4H20i
Nb and Ti in the Ti02-SO--H 0 system over a wide range of It
.) 2 2S04
concentrations (180 to 1000 g/litre) and the conditions for their
separation found. The separation of Nb and Ti is attained by the
successive fractional precipitation of Ti in the form
T:L2(SO03-HISOI,-8H20 and then the nioblum sulphate complex
(NH4)JTNb603(S04)l2j *21H20 with an acidity of 800 to
900 g/litre 112SO4, Th~ product of this process contains 98.26 to
98.8% Nb205 and 0.3 to 0.55' TiO2. As a result of this
investigation the above inethods are recommended for the separation
of Nb and Ti. There are 2 figures and 2 tables.
Card 2/2

)~ILYUTIM, M.I.; SPITIN, A.P.; SHAROVA, A.K.
Studying the interaction of trivalent titanitm sulfate with
sulfuric acid. Titan i ego spiavy no.5:301-396 161. (MIRA 15:2)
(Titanium-Metallurgy)

ACCESSION NR: AT4042095 B/2768/6i/000/007/0007/003.1
AUTHOR: Sharova, A. IL; Polyakovi, V. M.; Bamburov, V. G. j Chernpirskaya, Ye. L
TITLE: Separation of titanium from &0blum in mixed solutions of hydrof luoric and: sulfuric
araids
no. 7, 1963. Khimlya I
SOURCE: AN SSSR. Urallskiy filial. Institut khimil. Trudy
tekhnologiya redkikh metallov (Chemistry and technology of rare metals), 7-11
TOPICTAGS: nioblum, titanium, niobiumpurlfication, titanium purification, silicofluoride
method
ABSTRACT: - The authors studied-the mineral acid extrdetion of igglomeiates obtained d4r-
ing enrichment of complex ores by sintering with KCI plus K2SIF6 or Na2"';'F6 as well as the
separation of titanium from niobium in th4 resulting hydrofluoric and sulft-tric acid ~olutionb.
The agglomerate samples were treated at 70 and 80C with 3..6, 5.0, 7.,0 and 10% H2SO4' 1. 0,
2. 0, 2. 5 and 5. 0% HF, and their combinations, with or without addition of KC1 . Treatment
for i hour at 80-90C with a mixture of 1% HP and 5% H2SO4 was found to Im expedient, y1elding
up to 88% and 81% of the total Nb2O5 and T102, (plus ZrO2), respectively. Effective separa-
1/2 -
Cc4

ACCESSION NR: AT4042695
tion of titanium from niobium in these solutions was achieved by adding KCI to the solution
(up to 40-60 g/L11, cooling from 70 to 15C and allowing the precipitate to settle for 1 hr.;
94. 3-95. 6% of the total Utaaium* then precipitated. in the form of potassium fluorotitanate.
Org. art has: 5 tables.
ASSOCIATION; Institut kWmii,. Ural, skiy filial AN SSSR(Cheir-ical Institute, UrELL Branch)
AN SSSR)
SUBAUTTED: 00 ENCL..,00
SUB CODEt IC NO REF SOV-1 001 OTHER: 000
242-
C6r~

ACCESSION NR: AT4042096 8/2768/63/000/007/0013/0017
AUTHOR: Titova, Z.Mv Sharovap As Ke
TITLE: , A study of the conditions of precipitation of niobium from mixed solutions of hydro-
fluoric and sulfuric acids.
SOURCE: AN SSSR. Urallskiy filial. InBtitut-khlmil. Trudy*, no.' 7, 1963. Khimlya i
tckhnologlya rodkikh metallov (Chemistry and technology of rare metals), 13-17
TOPIC TAGS: niobium, nioblum oxide precipitation, silicofluoride method, niobium.
purification
ABSTRACT: The authors 'studied the conditions for the ptecipWition, of Nb,,O, from the
hydrofluoric and sulfuric a&d solutions which result from the processing of"pyrochlorine
concentrates by the silicofluoride znnethod, (concentrate: K2SiF6:KCI - 1:1. 6: 0.4 at 750C
for 1. 5 hrs. , followed by. extraction with 1% HF and t% H2SO4and precipitation of most of
the T1 as potassium fluorotitanate). Preliminary studies with ammonium. hydroxide showed
that complete precipitation of Nb In. achieved oiAy at pH lo. In MbSGqUent studies, RqU60US
sodium hydroxide solution was slowly added to the sample at 70-89C, in amounts so calculated
Zrd'

ACCESSION NR: AT4042096
as to leave a prescribed residual acidity In the sample. The niobium. containing precipitate
was separated by filtration, washed with water, dried and analyzed for Ti, Nb and.Zr. The
yield of precipitated Nb.was found to increase with a reduction in residual acidiV of the solu-
tion, reaching 97% for a residual acidity of 14.7 g/L H2SOj. An improved purification
procedure for tht, niobium, precipitate was also developed which requires less'NaOR and
yields a Nb 0 containing 3'. 65% Tio~# 0. 08% Zr02, 1% or more Cal up to 1%'Al and Fe, and
up to 0. 01;?M,g.. Orig. art. hast 2 tables,
ASSOCIATION: Institat khImit, Urallskly filial AW SSSR (Chemical Iwtltute, 'Uril- Branchj.
AN SSSR)
SUMUTTED. 00 ENCL: 00
SUB CODEt IC NO REF SOVi 009 OTHER-, 006

LCOSSION NR: AT4042097 S1 2768/63/000/007/0079/0063
1UTHOR: Sharava, A.K.; Mlyutina, IVLL
'ATLE: Separation of n1oblum and titanium (IM In sulfuria'acid solutions.
filial. Institu khimil. Trudy*, no. 7, 1963.' XhImly'
*UrtCE- AN SSSR. Urallskiy t a I
ekhnologiya redkikh metallov (Chemistry and technology of rare metals), 79-83,
:OPIC TAGS. niobium, titanium, nfobium purification, titanium purification, electrolytic
-oduction, titanium reduction
LBSTRACT: The authors investigated the possibility of separating titanium (ra) from qiobium
V) in strong sulfuric acid solutions on the basis of the Increase in formation of an Insoluble
itanium.(DI) compound with increasing concentratioa of the acid. A curve showince the yield
-f precipitate versus acid concentration Is shown in the Enclosure. Analysis of thc~precipitata
Jentified it as Ti 2(S04)3 2S04- 8H20. Solutions of 600 - 900 g/L H2S04 containing TiO2
nd Nb2O in proportions of 6:1, 4:1, 2-. 1, and 1: 1 were then used in experiments In which
6
he TiO -was precipitated in the above form by electrolytic reduction, while the niobium. re-
aained in the solution. The process is Mustrated by diagrams. Orig. art. has: 6 figures
Card, 1/3 *and 1 table.

ACCESSION NR: AT4042097
n
12
8
ENCLOSURE: Oi-
fVV 70V YOU YZ 5 04 214
Fig. 1. Decrease in the content of trivalent Ti inaDlution (in g/L) in relation to sulfuric
acid concentration (g/L). The Ti0i, cont6nt In the original solutions was 18. 5 (1). and
3 9 (2) g/L.
caid
'3/3

AT,
ACCESSION NR: AT4042098 8/2768/63/000/007/0086/0069
AUTHOR: Atilyutina, M. I., Sharova, A. K.
0
-TITLE: Fractional pro of titanium and niabium sulfates from aolutions of sulfuric
Wacid
SOURCE:. AN SSSR. Urallsidy filial. Inst.itut W
~imfi. Trudy*, no. 7, 1963. Khimiya I
-tekhnologlya redkikh metallov (Chemistry and.technology'of rare metals), 85-89
TOPIC TAGS: titanium, niobium, tantalum, titanium purification, niobium purifidation,
fractional prec~pltation, metal sulfate fractionation I
ABSTRACT: 'A solution containing 245 g/L H- SO 48 g/L TIO 10. 25 g/L Nb 0and
2
3. 52 g/L Fe 0 was used in a study of the succesiVve precipita&4n of titanium obium
in the form oi leir low-valence sulfates. - Titanium reduced electrolytically to Ti+3, was
precipitated (as Ti (604)3 - H2604 -by adding sulfuric acid to the solution to-a
2 8H20)
and Nb+
!'concentration of 800-900 g/L. The Nb+3' 5 remaining in the solution was then
precipitated in the form of ammonium, sulfite-niabiate,, 2]'. 21H20,
(NH4)8 "b603) (S04)1
C
7

ACCESSION NR: AT4042098
H.,
by adding ammonium sulfate to the aolution to a condbntration of 7. 5%. 98-99% pure
Nb 0 with less than 0. 5% T102 was then obtained from the precipitate In yields or up to
2
71.Rby oxidation
dryin,~ and calcining. 'Tantalum Is not
conversiqA into hydrates
,
,
preelpItated by the proceftre "The analyses'were carried out by Lhb. Asst. G. V.
Milovidova. 11 Orig. art. has: 4 tables.,
ASSOCIATION: Institute k1himil, UrallsIdy filial
AN SSSR (Chemical Institate, Urals,
,
Branch of the AN SSSR) A
.%
SUBMITTED: 00 ENCL: 00

IC,'IM
BUD CODE.- NO REF~ SOV; 007 OTHER: 001

2/2
Card

ACCESSION NR: AT4042099 2768/63/000/007/0101/0106
AUTHOR: Sharova, A. K., ghtin, A. P.
TITLE: The behavior of niobium, and tantalum phosphates with respect to various acid.
i -reagen
ts
SOURCE.- AN SSSR. Ukal'skly filial. Institut khtmil. Trudy*, no. 7, 1963. Kh1mlya I
tekhnologiya redkikh metallov (Chemistry and technology of rare metals), 101-106
TOPIC TAGS: niobium, tantalum, n1obium purification, niobium phosphate solubility,
tantalum phosphate solubility, selective extraction, oxalic acid, hydrogen peroxide
ABSTRACT: The solubility of niobium and tantalum Ohosphates, alone and combbied, in
2.3-13.6 N H PO 22.5-81. 0 g/liter of (COOH)2, 6, 9, and 12 N HCl, 3, 18 and 36N
H2 S04, and c&Xations of H2SO4 + 1-7 H,,O, or 4% (COOH) or HCl + 1-4% (COOH)2.
was determined in order to explore the pos;flAlity of their sXctivo extraction from a
mixture. The salts, separately or combined, were treated with a measured volume of
solvent without heating, the undissolved residue was separated by filtration, and the filtrate
Was analned for Nb and Ta. The two phosphates showed insignificant solubility in HQ.
WIL.
1/2

q
~CCESSION NR: AT4042099
Although Ta phosphate Is much more soluble than Nb phosphate.in high concentrations of
H3PO4, this could not be used for its selective extraction; in the other solvents and
combinations, the Nb phosphate was more soluble. Addition of 1-7% H 0 to H SO
4
7 sharpl increased the solubility of the phosphates, but their weight raia I the ffitrate-
y
remained constant at about 11!10'.7. Selective. extradtion of moblum phosphate cculd be
achieved only by treatment With a solution of HCI plus 1-4% (COOH)' in which Ta is
insoluble, although with H SO + 4% (COOH),:the NIJ:Ta ratio In theilltrate was 133:1.
2
Orig. ar*t. has: 2 figures &d tables.
ASSOCIATION: Institut khimffl Urallskiy filial AN SSSR (Chemical Institute, Urals
Branch of the AN SSSR)
SUBMITTED; 00 ENCL:- 00
NQ REP SOV: 008
UM C ODE: IC, MM OTHER: 008

ACCESSION 14R- AP4047787 5/02,89/64/000/002/0121/0126
U113La~ovaJ.A.; Bharov~~i A.K..
TITLE: nallium extraction from sulfu--ic acid solutions by means of methyl vinlet
11
S0U.-RCF: AN SSSR. SH rstmyp otdolenf.yn, Izventlya. Sartya khirnichoskikh nauk, no. 2.
1964; 1121-126
TOPIC TAGS- thallium extraction, Uiallium determination, methyl violet, quantitative
analysis
ABSTRACT: The reaction (in. v ~) 4 11 34- C I (m. v. )'11 C1 whore m. v. - vi t3thyl
violet.- was used by the autliors aj a metahod of separating Lhallium irlum sotlltioJ13 of
(:(?Mp!ey: compt-'s', res'441-nZ from di-~~-,Iving ;ubliniates of the nonferrous metals
indupfry in ffo~SO
- 0' 1 , - Inic pH of the solution, the thallium concentration, Ltle
n-eLh'v1 violet consumect, ;und 0-'e. rate o1 precipitate sedimentation %k-erp th c f,) i
'Prip amount of mtmthyl vblk,t irt
T.1 I
7 nc, j pq- < 7 in -iddidon tr >
primiarfly arg~nnc slikslano,,ac and n,-nUrnony, plus insignificant amounug o1 raner ~'L-ink-nLz'.
co. d L/i

Caro 2, 2

H -6
t 1.. P -4
-UR/4
FAP
AUTHOR: Chufarova, T. G.; Sharova, A. K.
TITLE, -Niob and tantal%un arsenites
-1-leorganic sl
SOURCE: Zhurnal he oy khimii, v. 10, no. 4, 1965, 877-982
r;TOPIC TAGS: niobium arsenite, tantalum arsenite, inorganic slmthesis
!ABSTRACT- Tn this work conditions were investigated for precipitation of niobium
tantalum from sulfuric acid solutions with sodium arsenite. Niobium pentoxide
containing 99.9% Nb205 and tantalum metal (99.9% pure) were used for making sulfate
sniutions. Niobium and tantaIum arsenites were precipitated by the addition of a
3--,Jium
:7- sl'fate solutiong containing a.-,talum an~
n:obium. On the basis of chemical analysis it was established that the composi-
~,-)e precipitate.-I ~.i*-,t`~,m arsenites may be expressed by the
Cormulas
2Nb2OS -As203' SH20 and M2.05- As203 -BH20.
LC.,d 1/2

L 522974-65
:ACCESSION NR: AP5009948
Keating curves display an endothermic effect at 1451C for niobium sait and at 1801C
for tantalum salt an(! Exothermi-- e"!--ct-s at 7300C and 9450C for niobium arsenite
an6 tantalum arsen--te T~)P endothermic effect is due to remc,,-),
of water from the salt whiie vie exother-nic effect ocCu--s ~!ue to trans-iDn -he
~salt from the amorphous to the cr-Istalline state. Hydrochloric acid solutions with
small amounts of oxalic acid as well as oxalic acid solutions containing potassium
chloride possess some select4-vity with respect to nicbium arsenite. Using these
s,~,!Iitions it is possible to obtain niobium solutions containing very little tanta-
11.1m or ~;Z, ig. ables and 5 figures.
ASSOCIATION! none
~4; 77r.~;: 27NOV~~ rMCL. 00 SUB CODE: IC) &C,

L 52373-65 FATW/ZP-F(n)-2/&WP(t)/W(b) Pu-h !jP(c)
ACCESSION NF: A,500991"?
TJR/0078/65"010/001-/0883/0888
AUTI~OR: -MilTatina, M. I.; Sharova, A. K.; Titova, Z. M.
TITLE: Niobium arsenate
SOURCE: Zhurnal neorganicheskoy khimii, v. 110, no. 4, 1965, 883-888
,TOPIC TAGS: niobium compound, inorganic synthesis, arsenic compound, chemical
reaction, precipitation, thermal analysis
ABS-PACT: The precipitation of nio-hium ar-senate from sulfi-iric acid sC)L1ti:)r'S was
h sr)(ji-jTr arsenalte. T- P;j-r -:,f
r- ~: Q, S 7
-.2~ 5 'irs e n a T
.of the Enc los ure I iZ -r~s 4~-r
-'niobi-um-.-aret...Ze-are:.15Q-300 g/X of sulfuric acid; about 4% of Na2tiAsGo".111-.2-
ticL; A6205 a IT624S.' lb-20). I I" Ag ng- of precipl ate:--fdr- -20- hrs-, - Hiobium arsenates
are forn*d by reaction of sodium arsenate with nioblum In sulfuric acid as follows:
(N-v07' ) ,.904 -11- Na:,q AsO. - (N401) ~HAsO4 + jNazS0,
Card 11/3

L 52373-65
rACCESSION UR: AP5009949
ana-lysiS +he arsenates and interm.~Iate dehydration products
-,c di"-
ca,cj- 2/3-

L 52373-65
A CC E: S So 1 ON AP 5 0 OTI: - 4
't
u C
time, hrs
acid sol'utiors a-9

SlUaM.I., .. F.
Sharovai, A. 1K. "On the rcl'~tlonship between L~10- structure and compcs!Llrn of Devoni,,,,n
Bauxites of the Ural 11 Trudy Corno-geol. in-ta (Ak-nd. nauk SSSa Orallskly filial)
p p
Issue 14, 1948., p. 74-80
SO: U-3`5-)~ 16 June 53, (Letopis 'Zliur;.al Inyl-h Statey, No. 5, 191M.

GLADKOVSKIYp A.K. : �WOVA, A.K.. VTORUSHIN,A.V.
Turgay Straits-Petrology, Rocks-igneous
Age of the igneous rocks in the central part of the Turgay Straits. Dokl. AN SSSR 83,
no. 1, 1952
Ural'skiy Gosudarstvannyy Universitet Im. A,M. GorIkogo
rcd. 8 Dec 1951
Monthly List of Russian Accessions, Library of Congress, August 1952. UNCLASSIFIED
S03 Monthly List Lf Russian Accessions., Library of Congress, 1953, Uncl

The AsWic CretwAous bawrite prcmictce. A. k. Glad-
-
k
"
d A
K
Sh
i
l
d
V
N

j S
R -
wi
arova-
a,
.
. ~
ddy.-I
ok
.-
auk S.S.S.R.
v
-
-Rprt
b
i
so
in
f A
m
S -im
s
eraccous
aux
tes o
swAlc
,
r
Rwmia havo a pb%ilitie strurture. The little wealwed

bauxite mcks con.6t of rM ernient and bla
ck inagoetite
-bt;us. The beans are built up with a finely di"r-ed lay
of magnetite of scdhn~ntary c,rixlu. nanmd &-inagnetite.
Four,varictfts of vibicrali are desiimated: A400.1-0~&
I HA A400.7-1.3 H.O. AIP.J,4-21.3. 11,0- and At^.3- -
UsO. The cheiti, wapit, of the bewls. the &beat, and the
'bawxite ii giveo. Another table gives the
of tile
CIZT
inagnetic fractious.' It ~% amunied-Utat tt"
;'
acjtnus;
,
bataltes are primarily a mech, and partly a chem. sedim6t~

~~kineralogicxl composition of batixites from the lower Cre-
PtaceouR Period in S.S.S.R. X77. , a kovskil suid A K
IMI,316
Dakfad
Akad
89
151-
Nauk S
S
S
R
.
.
.
.
.
,
y
_g~
,
(1) of the lower
Cretaccous Period himul in
.
U.S S.R. are composed of black magnetic pisolites (11) held
together by a rerlokh brown norunahnctic cement (111).
Oicin. and v)incr.%IoXicnlrf)mpni. of 11 and IH were tietti.and
the results showed that flawd Ill were fornuxl undcr different
physiro-chem. conditinns and that 11 are rimlly Ixtoxite
pebblex brought - to the I-Jact! of formatIm of I by cortalu
forces. Efixthet'i Mimbash

911
geov Olt
9p.
Ne
og?"'W; V. 9 -%O601
sooe,.
-IAO*
-10 0l
8:08
G.,L. ee -100
IP-49 t4 at$ leic, -0-0 VIVO- twe
VLOS Vo C
vplw~ k. 2 L I e OV6 tAC 1 Cs ce ajo-
110 *. - - ses-OlL . COO' we
for ~a, ;~~v k,
ev 0,0 dovP
COO so-tu 1,9~5
tsVIP eviel
IV b1
Tec~lo 1DOC~~ TO 0f a CeS t stsopl ti-StI6, tueo tis eels
Ve "e ext"clo S. ~Ooiool .11006 &Joe-as
~ Von Orr ae& as .ST,
ava IN -gsr~taa wa,~o cvat spo vodw- tve
eetto O'So Ue 00& j.31 toor5p
tip-, Coal tee Ne I
jj3o I - oirttl I
T 'bsV-a ~~q
tj~~o te (, ou r4,es Lee, me oTiov, aw Teo GO 2
jSOMP -refG
coq~--C-bog,~, -0 etAe '0., 6 t
SO 01 a oclou o VST
se
OT19~1 tUe Leu CIO OVA - et
C~aose yTev L jjt~ W~~s 50
eas d sovae 01:i
sa ol V
,Ole to' is, -lg~o
OT A's
OV, aa,cle .8*6.
CIA
vr SeCIN Ole"
t

Mineralogy and Origin of Bauxites
*TABLE OF 0
Foreword
PART I. MMMMM OF BAEMMS
Mineralogy of Sedimentary Bauxites (S.1. Beneslavskiy)
1. History of mineralogical investigations of bauxites
2. Alumina-containing minerals
3- Silica in bauxites
4. Iron-containing minerals
5, Calcium In bauxites
6. Magnesium in basixites
7. Titsmi- minerals
8. Sul:16r minerals
9. Phosphate minerals
10. Sodium and potassium in bauxites
11. Trace elements in bauxites
12. "Lode facies" in bauxites
13. Some problems of mineral formation in bauxites
14. Genetic classification of sedimentary bauxite minerals
SOV/1254
3
Card 2L3.4-

Mineralogy and Origin of Bauxites SOV/1254
Bibliography 49
The Origin of Aluminabearing Minerals in Bauxite (K.F. T*rentlyeva) 52
Bibliography 69
Mineral Composition, Origin and Metamorphism of lAwer Cretaceous
Bauxites of the Eastern Slope of the Urals and the Turgay-Plains
--(A.K. Sharova and A.K. Gladkovskiy) 70
Bibliography 71
PART II. GMWRAL PROBIM ON THE ORIGIN OF BAUXITES
A.D. Arkhangellskiyls Theor7 on the Origin of Bauxites In the Light of
Modern Science (G.I. Bushinskiy) 83
Bibliography 91
Regularities in the Dlistril~utl:on of Bauxite Deposits and Conditions
Under Which They Were Formed (Yu,K.Goretskiy) 93
Card 3yt]4.

- t- - j
-A -
Structures of Ural Paleozoic bauxites. mat.po geol.i pol.1skop.
Urala no.6:91-102 158. (kam 12: 10)
(Ural Mountains Ilauxite)

S',ii-LOVA, A. K. i- :Y, A. X.
Imegtones and 11,s Importance in prospecting for
Ural 1;mrorijim ~,,Ixjteo. Mat.w- pnj.lslOp.Urala nO.6:
103-11.0 158. (AIRA 12:10)

GLELI)KOVSKIY, A.K.; SH&ROTA, A.K.
Minerals framed during the weatberirg of bauxites in the Southern
Ural Basin and their role in the geophemistry of bauxites. Izv.
vys. ucheb. zav.; gaol. i razv- 3 no-7:130-1~4 J1 160.
(MIRL 13:9)
1. -Sverdlovskiy gorWy institut.
(Southern Ural Basin-Bauxites)

GLADKOVSM, A.K.; SHAROVA, A.K.
Regularities in the COMP00ition W Abftation of bwnite deposits
I in the Urals and the Turgay Maui. Troy 416r.-geol. inst, UFAN SSSR
U00582169-205 162, i (MIU 15t12)
(Ural Nomtains-Rumite) (Turgay Tabileland-Ilauxite)

GLADKOVSKIY, A.K.; SHAROVA, A.K-.
- nm--
,riassicn bawdtes on the eastern slope of the Urals. Dokl.
AN SSSR 151 no.6tl420-1423 Ag 163. (KIRA 16ilo)
1. Institut geologii Ural'skogo filiala AN SSSR. Predstavleno
akademikom D.I.Shcherbakovym.

SHAROVA, A.K.; RUDNOVA, M.Ya.
Strigovite from the Southem Ural bauxite baBin. Trj&f UFO
SSSR no,64:59-64 164. (MIRA 17:12)

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GLADKOVSKIY,, A.X.;_�_W0YA-k KHRAMTSOV# V.N.
Characteristics of the composition, origin, and char-ges of Yesvzoic
and Cenozoic bauxite deposits in the Asiatic part of the U.S.S.R.
Trudy Inst.geol. UFAN SSSR no.64:3.27-166 164. (MIRA l7sl2)

OLADKOVSKIYr A.K.; SHAROVA, A.K.
Significance of the facies primary and oecordar7 characteristics of
bauxites in forecasting. Trudy Inst.geol. UFAN SSSR no.64:167-176 164-
(MIRA 17:12)

GLADKOVSKIY, A. K.; SX~40YA_, A. K.
Bauxi-te potential of the Lower Mesozoic sediments of the eastern
slope of the Northern Ural Mountains. Izv AN SWR Ser ggeo-- 29 no. 5:
67-75 MY 164. (MIRA
1. Institut geologii Uraltskogo filiala AN SSSR, Sverdlovsk.