SCIENTIFIC ABSTRACT ANISIMOV, S. D. - ANISIMOV, V.
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CIA-RDP86-00513R000101620019-1
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RIF
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S
Document Page Count:
100
Document Creation Date:
November 2, 2016
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Publication Date:
December 31, 1967
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PUSTMNIKO~, Vasiliy GrIgorlyevIcb, kond. tek)LJ. 've"R,
Serge7 ThItriyevichp asfIrant
Electronic devIce for ermtrolling qtudlty Ln thcrmeti treatment
I
of ste6l. comporientge *1,-,v. rp. ucheb, zav.; eIrktromtAbs. 7
no.W,31-478 164 M-e, 17-7)
Is Fzradni slektrotekhnIki Rostovokof"~-,na-,)mu inst-limtg. Bel-'.gkr)-
khotyaystyannogn maahiriostroyenl7a. 2, L"svt,%IuyushChJy kafedrcy
elektrotekhniki Rostovskogo-na-1kinu instiLnta
nogo masbinostroyenlyd (for `~Ustynnikov).
PUSTYNNIKOV, V.G.; ANISIMOV, S.D.
Mul tiparam trio electromagnetic testing cf steel prc-lucts. Zav. lab.
30 no.10%1236-1239 164. OIXRA 1814)
1. Rostovskiy Institut sel'skokhozyaystvc-nnogo mashinostroyeniya.
ANISIMOVO Sergey DmitriyevJch, aspirant.
Formation of a multifrequency signal with considerLtiGn of
Information quantity. Izv. vys, ucheb. zav,; elektromekh. 8
no.4:437-440 165. (MIRA 18:5)
1. Kafedra elaktrotekhniki Rostovskogo insUtuta sel'skokho-
zyaystvennogo mashinostroyeniya.
28(0) PHASE I BOOK E)TWITATION SOV/2908
Anisimov., Sergey Fedorovich.
Chelovek i mashina; filopofskiye problemy kibernetiki (Man and Machine;
Philosophical Problems of Cybernetics) Moscow, 1959. 53 p. 24,000 copies
printed.
Sponsoring Agency: Obshchestvo po raaprostraneniyu politicheskikh i nauchnykh
znaniy RSFSR.
Ed.: V. F. Fal'skiy; Tech. Ed.: I. I. Zhernevskaya.
PURPOSE: Ihis booklet is intended for.those intei-ested in methods of control
and-communication applied to the analysis of the operations of machines.
CovERAGE; The booklet briefly describes the origin and development of cybernetics
and its current application in the analysis of the operation of such machines
as electronic computers. Some aspects of the theory of information, feed
back and self-adjustment of systems, and high,-speed electronic computers are
Card 1/2
ANISROV, S. F.
Chelovek i mashina (FIlosofskiye problew kibernetiki) ZF-an and Machine
(Philosophical Problems of Cybernetics),/, Moscow, 1959, 56 pages.
17,
ANISIVIOV) Sj~, and VISLOBOKOV, A.
"Certain Philosophical Problems of Cybernetics," Korx=ist, 1960, No. 2,
Pages 108 - 118.
S/057/60/030/009/019/021
A -POO 0 B019/BO54
AUTHOR: Anisimov, S. I.
TITLE: Heavy_Detonation in a Nonideal Gas
PERIODICAL: Zhurnal tekhnicheskoy fiziki, 1960, Vol. 30, No. 9,
pp. 1124-1127
TEXT: The author writes down the equation of state which describes the
substance in heavy detonations in a much simplified form:
1 1, bV 4- 0.625(bp)2 4. 0.2069(by)3 , 0.1920(bf)4] (1). 11, hin
P - yRTE
further investigation, the author starts from system (2) which describes
the central -symmetric motion of the medium. By substitution (3) this
system is transformed into systems of ordinary difforontial oijuationli
whose solution and integrals are thoroughly discusned. The essential
physical condition is the assumption that Cv is constant even at high
temperatures. Finally, water is considered as an example. As pressure in
(1) is assumed to be proportional to temperature, the author had to
Card 112
Heavy Detonation in a Nonideal Gas S/057/60/030/009/019/021
B019/BO54
restrict himself to sufficiently high temperatures. Fig. 1 graphically
shows the density-, pressure-, and velocity distributions. The author
thanks M. A. Yell-vashevich Academician of the AS BSSR, and Professor
A. S. Kompaneyets for discussing the work. There are 1 figure and 5
references: 4 Soviet and 1 US.
ASSOCIATION: Institut fiziki AN BSSR Minsk (Institute of Physics of the
AS BSSR, Minsk)
SUBMITTED: October 3, 1959
Card 2/2
F t preser."I at t~& %~fvrc-* on 4st &,' -.-mz:cr.
54
253. C~~,rre'l t
of
254. T. L. On Fmt !.Z Fi-- ~= the M",t i"t
of . Tube
255. 1. 0. Parts, Solutlom ol* S c-- Przbl~~ Witt F-tise Cr--tio-a
by CKIC.Es
256. S.I.tLn of So-~ Pr.bl- of Yotlz~ of
257. S. L. Dsnkov, On Comfo=al 71.-~~f~-nt.-oz of P~dl.tIons
vm~
258. ti.~ -6 CI---It1= or E-ti- or
Ac,;!2T:Nz; co.4-I.-
259. 1. A. )Ukk, Dzl..'~~ty of CyU~!rll~xl ftdltir~ V.
260. T. 11. V. H. F. R. Thlor~l or F--rrt',~
261. X. 1. TW~t==' cn Cal-u2At4ol Mctllc~d of Beat T~tzf~
-Waa=. Mg. of to. tZ 1-t
AgeAtl
262. A. V. Uvad r, N. A. Z~=ilov%clh v. P-74 I.-- i t L e
--c?7NYt-,;Oof th~ T!-Iest Sh-,~ , e.
265. G. L. 2.b.k~. ?~Ul~mxi-,es- n-d So--, of
M-,Z
264. L3.~l_ eat -1 A-a Tl-&~f~ , t 'oi-- Fre i -: F~rced
_Ce ViTnq, F - - - - -
265. TU. V. "Pla' F=st &n1 V.- ~r=sfer at %~-Wlcmt r~d of Cc~
Pro., Iai 6B at FOr.-,~m Su-t-e z---,Iy
266. A. S. Cll=-.-:~~/, Z. E. S:1~4klm,
-tr-z- -c~-
267. A.A
Cn t!. ae.- .14 Wl- ftr at
268. V. Zr. i. 3.zorilo" of
F
269. A. A. FaMaZ=t-~, 0.~ the TheCv, of %s!cr. &,d of & rdv
(The std;!= Prob--)
1.17-10
3161111
~W6 i/ooo/W6/62 1,/025
A001/A101
AUTHORS: Anisimov, S. I., Kuznetsov, N. M. (Minsk, Moscow)
TITLE: Self-modeling problem of strong explosion in water
PERIODICAL: Zhurnal prikladnoy mekhaniki I tekhnicheskoy fiziki, no. 6, ig6i,
167-168
The authors consider the self-modeling problem of strong explosion
for the case when disturbed motion is spherically sytnetric and temperature T
2
(at the shock wave front) exceeds considerably 3,000 K. The equation system
of central-symmetrical adiabatic motion in partial derivatives is transformed
Into a system of ordinary differential equations and its order is lowered by
using integrals of energy-and adiabaticity following from the self-modeling
nature of the motion (investigation of self-modeling solution was conducted by
N. N. Kochina and N. S. Mellnikov) and, after transformations, one differential
equation of the first order is obtained. This equation is integrated numerically
and the results for velocities, pressures and densities as functions of distances
traveled by the shock wave are tabulated and presented graphically. An equation
is derived which enables one to calculate the distance r2 traveled by the shock
Card 1/2
3 '~5 75 8
12Y62/00/003/037/052
D
D237 302
AUTHOiS: Yellyashevich, and Anisi-mov, S.I.
TITLE: Relaxation phenomena in high-velocity 1,!,-s flows
PERIODICAL: Referat"Lvnyy zhurnal, l.'ekhanika, no. 3, 1962, 103t
abstract 3BU'*69 (Dokl. Ali BSSR, 1961, no. 8, 5, 324-
326)
T~','&'T: A simple, approxi,..ate method is considered, of calculating
non-uniformities of flow in DrobleLiis of gaseous dyn,-mics. The me-
t',.od is based on the fact that in iziarVcases, inte.,-Posting from the
I)ractical point of view, the flow appears to be locally either al-
-.iost in couilibrium or almost stationary. The reason for this is
that the iiiie of relaxation Tj necessary for the thermodynamic equi-
librium to establish itself in various weakly excited degrees of
freedom, is very seldom temperature dependent. Also, characteris-
tic time of the gas-dynamical process T 0 which can be defined as
To = W(d VI/dt)-1 (W - specific enthalpy)p depends on the local tem-
peratures to an even smaller extent. ftence, the temperature inter-
Card 1/2
a S/124/62/OUO/003/03'1/052
Aelaxation pheno,I.,,ena in high- D237/D302
val in ~-wich 'r and -r0 are com-parable, is vory narrow. In the "ero
ap-.)ro,)*i.,.-.a'Uion in solutions of Las-dynamical )roblems it can be -MISSU-
-;~,ed th-t in the re,.-,-ions where - -1 'ro the flow is in equil.ibrium.,
vi'die for -c - - To it is stationary. The surface v:1,10.110 T=T 0 r COS L, 1:1-
bles the surface of discontinuity for the derivative da/dx whcre
a - a :.,.a,;nitude characteristic for an unstable processt e.- deFree
of 14issociation or enerGy of molecular vibra'4ons. At T-- -Lo, d_~ dx
= 7a/dx (7i - eauiiibrium -magnitude), while for T -~ To, da/dx = 0.
All the entropy changes concentrate on the surface cfdiscontinui'vy,
as ecuilibrium and stationary flows are isentropic. As an example,
the dei-.endence of the magnitude ln -r/TO on the x-coordinate is cal-
culate~ for recombination of oxygen in the flo,.,,, through a conical
noz:~lc. Initial tei-.,,percature and pres~,ure were 50000C and 0.1 atm.
The c-raph shows that a hundredfoid change of r/-ro occurs at a dis-
tance equal to the dianeter of - critical cross-section, i.e. a
Otationary flow ocours very seldom. 1,ore exact calcula't'ions can be.
-performed by the method of successive approxim-at ions, using the so-
luticn obtained by the above method, as a zero approximation. [Ab-
stractor's note; Complete trwislation].
C--rd 2/2
ANIS.r,OV S I
Stationary tc-npurature distribittion in conrectirn with a
cheniccl rcr~ctim. Do!:!. .':: DO'M 5 no.9:3,"l'-3t2 S 161.
14: 10)
L li!atltut AE DSM. ProCotavlono A14 BM
(TI't-r-re-I equati: I-is)
(Chemi6alreactions)
lo.1410 31726
S/057/61/031/012/013/013
B104/B112
AUTHORs Anisimov, S. I.
TITLEs Establishment Of Oscillation equilibrium behind a shook
wave
PERIODICAL: Zhurnal tekhnioheskoy fiziki, v. 31, no. 12, 1961,
1491 - 1493
TEXT: In the range of establishment of oscillation equilibrium, a flow
is described by the system of equations
PQ povel
p PV' P, -+- PAL
1=7 RT-j-Ej,
Vd-1* Sk (F) - 8j,
(PIT)
Card 1/5
-1726
S/057/61/031 012/013/013
Establishmelit of oscillation..* B104/BI12
where E kis the oscillation energy per unit mass, Ek (T) its equilibrium
value at the-temperatu-re T# andT-(pT) the relaxation times
A
-C(P-IT) .-- exp(B/T/3) is valid according to L. Landau et al.
O.IT6
j9T 'dowjetunion, 101 36, 1936). After introducing the dimen-
(Phys. Zee.ds /~ - V/V and carrying out.a simple
sionless specific volume V 71:6. 0
trannformation,
(6. d,
2
r0 7 j S(t) -#--I as-30 -b (3)
P. 2
1) Ap X0 8
log$ P2
[Lp~ ; -02
t. S
Card 2/5
1172
S/05 ~CO12/013/013
Establishment of oscillation... B104/Bli2
is obtained by.integrating the equation of motion. The index 11011 refers
to the supersonic flow, and the index 11211 to the equilibrium flow.
Quantities referring to the area immediately behind the wave front are
denoted b the index "I". Bearing in mind the above-mentioned funotion
for-t-9 X3~ can be integrated only numerically. With reference to a
paper by D. A. Frank-Kamenotskiy (Diffuziya i teplopereaacha v khimi-
cheskoy kinetike. Izd. AN SSSR, M., 1947), instead of (3),
b.=&
T 69)8
I (t 4' (6 20-1-
X dt,.
is obtained, where z F_+ t, CR is the specific oscillation heat
oapaoity,'and k - (BR .1/3/,2/3 )/S(a-2t)/qa_ 84/3~ . This integral is
0
Card 3/5
31726
5/057/61/031/012/013/013
Establishment of os6illation.e. B104/BI12
given in.tables. For the case of strong shook waves,
7-1
3~4'
9, e-..IT. El[~7k(V"
(A)
ia obtained# whore Ei(-x).- I t /t. Terms of tho orda'
Oj a- dt r of
E)2
The solution
0-00ITare,negleoted.
iaV-3VI-b
2
P VO
(6'V - -2i V -d 7
T= V).
of (1) is given for investigations where the relaxation L-o of the gas
is determined from the experimental density distribution I,i~)iind a shock
Card 4/5
88404
S/020/61/136/004/012/026
,5?,~,600 (olso //'/.3, /1/,k7,) B019/BO56
AUTHOR-- Perellman, T.L.,. and Ani8imov, S.I.
TITLE: Density Distribution of Charged Particles in Meteor Tracks
PERIODICAL: Doklady Akademii nauk SSSR, 1~61, Vol. 126, No. 4, PP. 810-812
TEXT: For the purpose of studying the reflection of radiowaves from
meteor tracks it is necessary to know the density distribution of charged
particles. By diffusion, recombination, and addition of electrons to
neutral atoms and molecules, density changes, the latter effect not chang-
ing the density distribution, but the effective recombination coefficient.
The relative effect of recombination and diffusion upon the density dis-
tribution may be expressed by the dimensionless parameter 6 = CAq/D, where
a is the recombination coefficient , q the number of ionizations per unit
length of the meteor track, and D the diffusion coefficient. A differential
equation is given, which describes the density of charged particles pro-
ducedtyameteor moving with uniform speed:
Card 1/3
Density Distribution of Charged
in Meteor Tracks
n /~, t - D~-
r(r-0-r)
n (0, t ) <
88404
Particles S/020/61/1%/004/012/026
BO19/BO56
an + '7 )h(z - vt) (2)
21 v r
0
n(po,t)0
This differential equation may be calculated by means of the perturbation
theory in the case of smallE. With & being greater, the perturbation
theory is not applicable, and an approximation has to be found. The
authors discuss the two methods of solution and obtain expressions describing
the time dependence of the number of char,~ed particles. They thank Acade-
mician Ya.B. Zelldovich for valuable advice, as well as Member of the AS
BSSR M.A. Yellyashevich, G.L. Barenblatt und Yu.?. Rayzer for discussions.
Theresm 3 references: 23oviet and I US.
ASSOCIATION: Institut fiziki Akademii nauk BSSR
(1nstitute of Physics, Academy of Sciences BSSR)
PRESENTED: September 1, 1960, by Ya.B. Zelldovich, Academician
Card 2/3
88404
Density Distribution of Charged Particles
in Meteor Tracks
SUBMITTED:
July 22, 1960
S/020/61/136/004/012/026
B019/BO56
card 3/3
:-'0 7 2 /0 C C) 0 1 1 1
1314 5/B 138
AUT11011'"' Anirimov 13. 1. Rovinov G. S.
TITLI-:. Nonequilibrium flow of air in nozzles
I `,10 C' D I C.." L -Zhurnnl prikIndnoy mekhan4.1- i i te';Iinichosko.-; fi7,il.-i, a. 1,
n
1962, 76 - 81
T',;i'.T: The article deals with some pioblr-r.3 of the kineticg of adjustinf~
equilibrium between the trarislv+ory 8,na inert deUrees of freedom of the
molecules in air at high tempey)fw.-e- rhe following 31ow processes which
occur in nir at high temperaturCs are studied:
0 + 0 + hi '~ 01 +,Af
N +N + hl-- NI+AI (2).
N + 0 + hi -- NO 4- M 0)
0 + Np NO + N (4)
N + 01 NO + (1 (5)
Os* + M 0- -F
$
N
It N: (6)
7
,
+
C 1 / D6 (
)
3/207/62/000/001/011/1018
Nonequilibrium flow of ... B145/B136
Since thore is up to 150-20T,'L~ uncertainty in the rate constant values (1~
rate constant of the go-reaction, k of the return reaction), SoMe Sir;Pli-
fications ari made: L', any molecule or atom, is ec'ually effective las third
body during recombination, the contribution of NO to the total enerey and
total pres:~ure is neglected and (d [NO /dt) 0 is assumed.
1 3,4 5
The effect of the vibrational relaxation on the rate of recombination may
be neplected when the condition kCrlC~~,11 (k rate constant of the reaction
M + 0-K --->O + 0 + M, ~ density, Z, mean molecular weirht, i~ relaxation time)
2 1
is satisfied. If the weight fractions are denoted byc< i (i - 0, N), the
dissociation energi-es by Di, and the equilibrium energies of vibration by
~.V usinC the equation system ~vA(x' - const, dp/dx i- p dv/dx - 0,
2/,)4. 0
h0 - h - v 2 (18) (A(x) nozzle cross.section) (for a one-dimensional
flow without diffusion, friction or heat exchango, one obtains the equation
Card 2/6
3/207/62/000/00'/Otl/olb
B145/B138
Nonequilibriu" flow of ... a *
daO j(j.5T + Do - 8.) P (ao'aW T) - Tj + J.142 I(J.5T + DN -
7r- j.53to + 1.71311s + 3.882) F (Oto, 'Is, T) --
T) - Tj + Lr 1(
s) F (m0, IN t dx
211ol +!-'0 (0.233 - do) Ott' -
dx
21L0 7' dA
+ i.02~6-N (0.767 uN) F (ao, Is, T) + --A-d,
IL
dr
RK T
F 2j7~h h))
kinetic 04uat'ono
-which, tc)gether with the
Cnrd 3/6
Nonequilibrium flow of ...
S/207/62/000/001/011/016
B145/B138
fra 0 2P 0.233 - ao ao2pN ~a
-- =- - - kjo + [.k P N 0.233 CEO)
iTT - I V 6 - kl'OCO I NO]]
VjKh 2 ~i V 2111; -
4ictm 2P 0.767 -etN 2 PM* (0.767
(kg kg' k,'a, [NO]
CF ti, ) +'T [k,
;r VP ,2 2P0 d (2P)
8ACC16
deo eo (T) -so deN BN (T) er,
ZT 7 -r-0 -(V.-pT W- 7 -rk -(T-;-p-F
NO p US' agmop k~cto (0.701.- a'N) + kali (0.2~3 ao)
2 )~P0N / it + kj'aN1,D + ka'aOILN
forms a closed system, the integration of which requires numerical methc)d.,j.
In the case of a "p' ,artial freezing in" (vibration in equilibrium, but
without change of gas composition) the following solution is easily ob-
tainedt
Card 416
3/207/62/000/001/011/018
Nonequilibrium flow of ...
B145/B138
0-5*0+0.fi71mN+2.77,3
A T 00+1-1424N+1-109 X C
71-. T 1/ 2 (ho - h) x
xCxP (0.233 - ao)Uo* - /0) + t. 142.(0.767 - a1q) (IN* IN)
a0 + 1.142aN + 1.109
(25)
. )-I . 1,
h=L, I-OxP T - In OxP T
T (
The asterisks denote quantities which are variable, in the critical- cross
section. The vibration was assumed to be harmonic. In the case of an
equilibrium flow it is best to start from the changed Eq.
2
0 0 *1 , since inteUration
IvA(x) - const, h - h - v 12 - 0, 6 - 3 (0. entropy)
of (21), (P2) leads to unclear solutions. Calculation of the system (21),
(22), by moans of an electronic computer, for some concrete values of the
initial densities and temperatures, sho-.-jed that the devintion from equilib-
rium is hi~-,h for no-les of about 10 cm, and that the, approximation of the
"fro~en-in flow" is better than thnt of the equilibrium flo-e.-. Ya. B.
Card 5/6
S/250162/006/001/001/002
1028/1218
AUTHOR: Anisi hodyko, Yu. V.
TITLE: Convective diffusion in the boundary. layer in the case of flow inside an angle
PERIODICAL: Akademiya nauk Belaruskay Doklady. v. 6, no. 1, 1962, 19-21
TEXT: The flow in a dihedral angle formed by plane plates is considered, and (he equations of convectivc
diffusion in its boundary layer are solved exactly. The differential equation describing the distribution of the
concentration c(xy)
v. aclbx + v, ac1b), = D dlrl~)-2 (1)
is integrated, and its general solution is given. Two simple particular cases are indicated: a) for C(X,O) = CO
const, &,y) = co; b) for c(x,O) = cox -', c(xy) = roar , . U(q ; n)lu(O , n) where n = y1X FR-el-2i + lo.
ASSOCIATION: Institut fiziki AN BSSR (institute of Physics of AS BSSR)
PRESENTED: March 20, 1961
Card 1/1
ANISIMOV, S.I. (14inak); PERELIMAN, T.L. (Minsk)
A nonlinear beat transfer problem. PHrF no-5;136-139 S-0
163, (MIRA .16.-11)
ACCESSION NR: AP4004149
S/0294/63/001/002/0276/0280
AUTHORS: Anisimov, S. I.; Nogotov, Ye. F.
TITLE: Steady-state theory of a thermal explosion
SOURCE: Teplofizika vy*sokikh temperatur, v. 1. no. 2, 1963, 276-
280
TOPIC TAGS: thermal explosion, thermal explosion stationary theory,!
temperature distribution, iteration method, temperature jump, 13teadyl
state theory, explosion
ABSTRACT: The conditions under which stationary temperature distri-q!
bution is possible in a medium containing temperature-dependent heat's
sources is analyzed mathematically, with a particular aim of deter-
mining the critical dimension of the region containing the heat
sources (D) beyond which stationary temperature distribution becomes----
impossible tthermal explosion becomes possible). The problem re- .
duces essentially to an investigation of the existence of a solution!
of the boundary value problem At + qf(u) - 0 in the domain (D) with
Card
ACCESSION NR: AP4004149
U = U0 on the boundary of this domain. It Is shown that some re-
sults can be obtained with the aid of known existence and uniqueness
theorems for the solutions of integral equations. By way of an ex-
ample a detailed analysis is made of the one-dimensional problem
T1 + q exp(-l/T) 0; 0 < x < 1
T(l) = To, TI(O) 0
(T - temperature in units of activation energy E, q Q12/Ek - dim-
ensionless parameter, in which k - thermal conductivity of the med-
ium, Q - intensity of heat release in the chemical reaction, and I
- dimension of the vessel) for which uniqueness and existence con-
ditions are obtained. 'In conclusion the authors are grateful to
M. A. Yellyashevich and A. S. Kompaneyets for a discussion of some
results of the present work.' Orig. art. has: 10 formulas and 1
table.
ASSOCIATION: Institut fiziki AN BSSR (Physics Institute, AN BSSR)
SUBMITTED:,. O7Jun63 DATE ACQ: 26Dec63 ENCL: 00
card
ANISIMOV, S.I.; ROMANOV, G.S.
I.-- ", -- - ---
Kinetics of the decay of two-atomic molecules in the absence
of vibrational equilibrium. Dokl. AN BSSR 7 no.6:376-377 Je 163.
(MIRA 16110)
1. Institut fiziki AN BSSR. Predstavlsno akademikom AN BSSR
M.A.Yellyushevicliem.
ANISIMOV, 5.1.
Effect of vibrational relaxation on the dissociation rate of
diatomic molecules. Zhur, fiz. khim. 37 no.1212754-2757 D 163.
(MIRA 171l)
1. Institut fiziki AN BSSR.
ANISIMOV, S.I.; KHODYKO, Yu.V.
Flow of a gas with delayed vibrations past the frontal critical
point of a blunt-nosed body. Zhur. tekh. fiz. 33 no.llsl333-1337
N 163. (MIRA 16:12)
1. Institut fiziki AN BSSR, Minsk.
~'3 M;
al
96- UPT V.
Md
-dl
ww nu,
n4
.0 tow
qm-
-mi
. .......... JR,
-P-ft-bU
VIP
M
'M"W"
OWN!-,
IN A k~
W N
I
0
. or
C.-I
U
ACCESSION NRs AP3003176 1
a/M50/63/007/006/0376/0377
AuTlIoRs': Anisimov, S. lei Romanovi 0. So
TITM On kinetics of diatomic-molecule dissociation in absence of vibrational
equilibrium
SOURCE: AN BSSR. Doklady, V. 7, no. 6p 19631 376-377
TOPIC TAGSs rotational-equilibritim) vibration relaxation$ dissociation rates
diatomic molecule) vibrati-on equilibrium, Boltzmann distributions vibration energy
ABSTRACT: On the assumption of rotational equilibrium, the effect of vibrational
relaxation on the dissociation rate has been studied in diatomic molecules* The
case of small deviations from vibrational equilibrium was considered) assuming a
Boltzmann distribution for the vibrational degrees of freedom, with Wmperatttre TO
slightly different fron the translational temperature Tv orj, for a - T-TO/T
whore 5 and-la - arithmetic mean of vibrational energy in
. (7)-
Card 1/2
ACCESSION NR: AP3003176
interval (N-m,N). The largest effect caused by vibrational nonequilibrium has been
evaluated for the distribution f.unction f0 0 . Orig. art. has 1 6 formulas.
1" 0.
ASSOCIATIONs Institut fisiki AN BSSR (Institute of Physics, AN BSSR)
SUBMITTEDs O1Nov62 DATE ACQ: 24jul63* ENCLs. 00
SUB ODDRs AI NO REF SOV: 003 OTHERt 000
Card 2/2
Arcnssm NR: AP4028948
AUMOR, Anisimov, S. 1.
S/0057/64/034/004/0620/0623
TITIX: On the non-monotonic variation of tomporaturo and donsity behind a strong
shock front in a gas
SOUXEs Zhurnal takhnichealcoy fiziki, v.34, no.4, 1964, 620-623
TOPIC TAGS: shock wave, shock wave temperaturo variation, shock wave density varia-
tion, inert degrees of freedom, relaxation procossos
ABSTRACT: The variation of temperature and pressure in the non-equilibrium region
behind a shock front is discussed qualitatively. Following Ya.B.Zel'dovich and Yu.
P.Rayzer (UFN 63,3,1957), the author calls a degree of freedom "Inert" provided its
relaxation time is long compared with the moan free4light time 9f a molecule. it
is the presence of inert degrees of freedom (molecular vibrations, dissociation,
electron excitation, etc.) that gives rise to extended non-equilibrium regions be-
hind shock fronts. If the relaxation times of all the inert degrees of freedom nre
distinct and remain so throughout the whole non-equilibrium region (they are func-
tions of the pressure and temperature), the temperature falls monotonically from its
Card 1/3
ACCESSION NR: AP4028948
value immediately behind the shock front to its equilibrium value far behind*the
front. If, however, the difference between the relaxation times of two inert do-
groes of freedom changes sign at some temperature between the initial and equili-
brium values, the temperature may pass through a minimum within the non-equilibrium
region, and if thotio two inert degrees of freedom are the only important ones, It
will indeed do so. In this case the density will pass through a maximum if disso-
ciation processes are not involved, and it may 4)ass through a maximum if such pro-
cesses are involved. The case of dissociation of oxygen and excitation of nitrogen
molecular vibrations is adduced as an example of a pair of inert degrees of freedom
satisfying the required condition: at sufficiently high temperatures the dissocia-
tion is the more rapid process, but since recombination takes place via threo-body
collisions, it may become the slower process in the cooler regions. An explanation
of observed non-monotonic temperature and density variations offered by A.Resler
B.Cary, and J.Logan (references are given only to Russian translations) is criti-
cized, but the discussion is too brief to.pormit a judgement to be formed concern-
ing the merit (or'evon the nature) of the rejected explanation. "In conclusion, I
express my sincere gratitudi to L.R.Gurovich and YuoP.Rayzor for discussing the
present oontrib%itions" Orig.art.hassl 7 formulas.
Card2/3
3/3
Card
ANISIMOV, S.I.
Thermal explosion problem for a hollow cylinder. Inzh.-fiz. zhur.
no.11:115-116 11 164'. (MIRA 1~~:2)
1. Institut fiziki All BelorusBkoy SSR, Minsk.
Cj
-11M
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ANISIMOV, S.I.
Solution of integral equations of open resonators. Opt. i
spektr. 18 no.3:522-523 14r 165. (MIRA 18:5)
ANISIMOV. S.T.
growth equation anj same other iynamic systems modeling
biological objeets. Blofizika 10 no.2062 165. (MIRA 180)
1. Institut fiziki AN BSSR, Minsk.
A
F 12T3/1284
I j- -? -
;AUT11OR: Anisimov S I., Bonch-Bruyevich,A.L'.; Yel'yashevich,M.A.; I=s,Ya.A.;
Pavlenko,N.A_.; Romanov,G.S,.
ORG: none
-ITLE; The effects of Intense light beams on metals
__jRCE: Zhurnal takhnichaskoy fiziki, v, 3G. no.7, 1273-1284
TOPIC TAGS: laser effect, metal melting, metal vaporizing, heat of sublimation
ABSTRACT: The authors have investigated theoretically and experimer
#ally the Phan-
omena accompanying the di.sruption of metals by focused laser beams.16In the present
paper there is considered the case of a laser producing approximately
I millisoc pulses, each consisting of a sequence of approximately 1 microsec spikes.
The phenomena accompanying disruption of motals by, iant laser pulses will be discussedl
in a future paper. In the theoretical part of the paper, fluxes of loll to 1016erg/cm2i
sac on an approximately 1 mm, diameter spot are considered. It is shown that under
these conditions the transport of energy in tho metal by heat conduction during the i
duration of a spike is negligible, and the problem of the vaporization of the motal is
accordingly treated in one dimonsion. Formulas are derived, and curves are presented
for different metals, relating the energy flux in the laser beam, the temperature of
the metal surface, the erosion rate of the metal surface (i.e., the rate of increase
Cnrd 1/3
L ;o
ACC NR: AP6025256
in the depth of the hole), and the velocity and pressure of the jet of metal vuor.The
Ito,mperaturo of the metal surface is not equal to the boiling temperature, as was Orro-
Incously assumed by J.P.Ready (J. Appl. Phys., 36, No.2, 462, 1965). The thourotical
relations were tested by experiments on some 16 metals and alloys, using neodymAluln "
~glass lasers producing up to 300 J pulses. The laser beam was focused with a Ions onto
!the parallelepipedonical specimen and the disruptive process was recorded cinomat-
ographically at 105 frames per sec. In most of the experinents a glass plate was
cemented to one face of the specimen and the laser beam was so directed p.1ralle'l to the
glass-metal boundary that about half of the beam passed freely through the glass and
the other half penetrated into the metal, vaporizing it. In those experiments the
process was photographed through the glass. The mass of metal removed by the laser
pulse was determined by weighing the specimen, and the impulse due to reaction of the
metal vapor jet was measured. The experiments were in qualitative agreement with the
theory, and quantitative agreement in order of magnitude was found. The authors feel
that development of a more accurate theory would not be worthwhilQ, owing to the large
variations between different lapers. Three stages were distinguished in the disruption'
process: in the first stage.J~e temperature of the metal surface increased at the rate
of approximately 1011D degree/S'ec; in the second stage metal was vaporized from the
specimen and a hole was formed in it; and in the third stage a pressure of 102 to 103
atmospheres developed within the hole and a powerful jet of metal vapor issued from it
at supersonic velocities. The ratio of the laser pulse energy to the mass of metal
2/3
L 4o385-66
ACCNR% AP6025256
lost by the specimen was approximatoly equal to, but in most casus somewhat less than,
the heat of iublimatioij of tho mutal. Aii appreciable mass of tho metal was ejected as
liquid. Orig. art. has: 9 formulas, 11 figures, and 2 tables. [151
SUR CODE: 20 SUI-311 DATE: 263un65 ORIG. REZF: 005 OM RFF: 004
ATD PRESS: Sd
C.,d 3/3 vmb
L 09326-67 .1 p (m) /:,71jr (1,) /-rg: v,,t/jlq/j CODE i-bw
XCC N W, AP66~*0954 On, C E 0207/`6/ooo/oo4/ol5o/ol5l:
IX-.i-Oil: alalMa, So 1. (minsk); Vitkin, E. 1. (il"inGIA
GIRG: none
V,
TITLE: Some variational problems of the theory of "ermal explosions
SOURCE: Zhurnal prikladnoy mekhaniki i teldiniclicskoy fiziki, no. 4, 19606) 150-151 1
TOPIC TAGS: thermal explosion, variational problem, nonlinear differential e =ion,
approxiza-tion method
ABSTIViCT: / The authors point out that most of the results obtained in s tat4 i o na i -y thcL~~
ry of -thermal explosion pertains to Bymm, ctrical regions, in' which the temperature dis-i
kribution depends on a single space coordinate, whereas practical problems deal wit.11-1
two or three independent variables, for which the nonlinear partial differential equa-f.
tions are dif-ficult to solve without a tremendous amount of nimicrical calculations.. I
TV is shown, since the solution:; of physical interest are on)Z~ thoze correspondi,-4",
to low tcmpera-I%-,uxcs, that the calculations can be simplified by approxi;matinz the ex- I
poncntial temperature dependence with a trinordal. The application of this approxi.-k-4-,
tion to the variational solution of problems involvinG a cylinder of finite lenrh) a.
rec.tangle) and a 'p,~rallelepiped show satisfactory agreement with results obtained by
others. Oria. art. has: 11 formu-1as.
SUB CODE: 20/ Sum DATE: 17yay65/ ORIG REF; 004/ 0-,,j REF; 001
Card
ACC NR,
AT7000377 SOUtCE CODE: UR/0000/66/000/000/00~6/0!03
AUTHOR: Anisimov, S. L; Khodyko, Yu. V.
ORG: Institute of Physics,AN BSSR, Minsk (Institut fiziki AN BSSR)
,TITLE: -Convective diffusion in the boundary layer with flow in an angle
'SOLRCEt Teplo- i massoperenos, t. 6: Motody raschota i modelirovaniya protsossov
teplo- i massoobmena (Heat and mass transfer, v. 6: Methods of calculating and
inodeling heat and mass transfer processes). Minsk, Nauka i tekhnika, 1966, 96-io3
TOPIC TAGS: laminar flow thermal diffusion, mathematic analysis, boundary layer theory!
ABSTRACT: The article presents an exact analytical solution for the equation of
~onvective diffusion in the laminar layer with flow between non-parallol flat walls.
-In the mathematical formulation of the problem it is assumed that tho liquid 15
incompressible and non-dissipating, and the concentration of reacting impurities in the,
.flow is small, so that any change in the parameters of the flow as a function of the
composition or the temperature can be neglected. nie coordinate system 13 chosen as
.shown in the figuro. With the usual assumptio=, of the theory of the boundary layer,
~he system of equations, which can be integrated, can be writtin in the form:
Card
: ~ N I '-') / A- f ( ~ V,),I-~-l .
VMTBIMIKOV. A.1.,- ANISINOV, S.14.
Iq)rove land recorde. Zemledelle 6 no.1:83-84 Ja 158. (MIRA 11:1)
(Omak Province-Yarm management)
I I loll 00 'loll" "', I'M I'll 11 "1, a at 6) 41 or:
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in the
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.00
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Olip eoln
litne$ 04 Inuth'Ll IM' C11'01 NII %#lit .
00 .
tiptitlaills 1,1)c(,%, 0.310
"
6 111,S). Treat the new residue with 2% NzOll (the %olli. 0o
untains IvbCW,, and U-3-0 4% it( Ilt;.CI(1'0.)s) Attain
c'
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i
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.
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.
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t
I
d
P
f
h
, tk
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l. Duf -
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I %tn. due tit the formation o
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themes air co%vied with a PUS Win. Such ertors can lie
ignmed since the still. of I'M is Itivreaw-d very Indr, suit
its filin dives nut hinder the reactions with the miltivi.
W. R. Ifenn
00
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6499
ANISIMOV, S. ., GURIYFV, A. R.
IMSR
Professor, Candidete of Technical Sciences
~The Sintering of Lead Sulphite Cakes"
Tsvet. I-let. 14, No. 10-11, Oct. - Pov. 1939
Report U"1506, 4 Oct- 1951
?I few It i i i i i i i ; i i i i 1111.
for*
004 1
00 -00
00A CA
AsObsura n otsistc suffste caskev S
A. r
t rsvdnyf Metal. 19i
of U.-The ainterinS of cakes of kid sullate from Cottrell
precipitator ditst With Coke. with or without addit. (A 111i
pl
roncentrates. was studied. The first series of expts. with
of tj! suffate cakes frorn Cottrell dust and coke showed that the
00 41 , il, optimum rewult4 can be obtained by u4nit coke in aultt~
of 3-4% of the wt. of the charge. and 13-20 cm. thick".
00 of layer. The total S remaining In the product is 0.8-
1.7%, which Indicates de2ulfurization td about
The devm of decompa, of vullate Is about 100%, aml the
products am Ph oxide and sulAde. and metallic Ph. Dur- -00
0 ing the sintering. 2-10% of the Fb is feduerd to metal. Goo
The av. vertical speed a( the sinterint prtKv%s is 2.:1 cru.
per min. In the second series of cipts. sulfate cake was coo
::W mixed vrith lab concentrates and tuxes, and subjected to
doulile roasting. In the first roasting O-R% of the Ph in
the charge was reduced to metal and in the second 30% cd
I the remainder which Is 3311% of the total l1b in the
coo
charge. 7%e first product contains 2.5-4% and the OW
imsduct. 136% of the tote] Sin the ehjace~ TheinitWS Q*4111
cocitent In the charge Is 7.5%. T'he vvtlk*l spred of 9*0
toasting is 1.7 em. per min. In the first aed 2.4 em. per
min. in the wond stage. Sintering of materials contg. lvo
sulfate and reduci tsmelting of the agglomerate can suc-
cewully te 0.1 It other methods of etin. of Ph from
I hese, M at= n. N. Wniloff
101414.1 "it G.. cog OJAW am o- M
U U Alf go A 0 1 1 1 1 1, F I-V a I TiU
0 0 0 4 8 6 9 9K.4 U It R IUD ft I I FA An I 1 0 nd 0 0 a I W in 0 a 0 3 2 v
0 0 * 0 **so** 0
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I,
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lee
"witting sise drom with Itad loacentrates -M
Atuslivoiltv asW A N Omirv ll,ud NO.
I V. I JA. X%1,
J-1.
lee
1% "NIVC11ttAIC, Wctr dd,jrd. J'he Ztl drim
Ztt. the charge was %milmatatilly
kIW in 8 and hall 114) Pyritic rt~m, vitpl,
0
it is eugivilidecl tholt Iniqueltillit In me stagr (cycle) with
::
227P Zoo dram 61, Or chat lllll~ .1194 will hirl.
*
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fIx lot meth4likod %imisill
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11111 StAgr g*VC lallidlk-Wfy lr4UII4 still# %V)VU JIM* In the
00 .3 charge. Sume. I%v(,ut t-rultict- Wet, -Ntwi-d Uh,
4
14-1,118 viviv c'.11111111vit I-V plAill wAte C%1.1, P Irfel
VIRTS. It. N. 1'4ntl.fl ZOO
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A[11 IL-6 a __L a A 1-1- At aF a A A V. 1 2 -M SO qx 0 ttfs--k I A tf a k 4 1 - a a & -1 A.
00 4
x%p
Agoomeratiou and arittiting of zinc calrea with lead -*0
of oil
VOCIC"trates. Rotov. 1"Vjft)W
oto Metal. MO. Va. P 4t'_*== Jratc% an.1 Zn cakes
iz of c1cctrolytic Zu works roasted on the Dwight 1.1.rd ma-
chin" gave an agglomerate conig. 1.2% S. 11(iwrvrr.
this has not yet been satisfactorily smelled. ll~N.D. -00
00
00 ro 0
1re*
iro 6
zoo
!zoo
so*
tit
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"
-Z'.t4p 1.
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p.*-
HMWM 1111iffitiNtim with IftakH,SO,. S. M. Aum. lee
00 2;
1 TIMT- IJ`TWIW.W -IfOrt-11. 10. XI 111V41); (VIR. It'llf. lee
11043. 1. :.a l(l. -Miany CLpt%. litarre callictl anit math dill".
cut Linda of sulfiak tw-, Th. ti-te.unt ot. -00
119SOo itt-quitral varying quatititt- tal achl All.1 dlarl'.111
Z tesupla. in antler to oblaso t, hiotol.o. W 0., %ail.
60 a fide. Particutarly, with Co.,; and pytitic orj.4. A% a tok.
j
0 sood ir-tills were obtained by ti,-Awill 'ais g. oil ..tv ..as.
9
t,entratte with 12.1 I.Witil. of sin"A atid lw.iting tat re
:
** 0 Co
00 41KI 4.'vil* in it trauffir furn*v lot 441 NI total. Thco ilar too
00 gray product wds extd. with 4(K1 itil. of All I f#Aj,. Front
thrituhit
i 'th
Ag was I-pid
b
"fin
KCI
A
0900
.
.
ant
y
e
g
u wasdetti.
!n1heresialue. The final conclumon drawn from the work goo
bt that the treatment with i(tR)4 is advantageous. The
lustiest in lialaill Al and All star Arnallei than by the umm
toolicidtaolthyatsayandin i lie enal l," tittle i. tv,pliteal
W. 11. 11
MITOLIUR&KAS 1,1114"I'al C"ll'"Atles
U"a Lf
I let., 61-V!W
101m, .11 0..
a 11 V-1
ad 0 a 0 1 W W
a Kill A I ILAI
U 9 0 it
0 0 41,
9 0 111 0 0 0
0 0 go 0 0 0 0 0 0
0 0
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see
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use
WOO
WOO
aISIMOV. S.M.; TRR=, EV, V.I.
Scientific ana techniqql student conference at the Northorn Caucasus
School of Mining Enginbering. Izv.vya. ucbeb. zav.; tsvst. not.
no.3:153-155 1 58. (14IRA 11:11)
(Caucasus--Mining engineering--Study E,,nd teaching)
SOV/149-58-6-6/19
AUTHORS: Anisimov S.M. and Dashkov, N.P. (Deceased)
TITLE: 4oasting and Sintering of Zinc and Lead Concentrates in
OxYgen,enriched Air (Obzhig i aglomeratsiya tsinkovogo
i evintsovogo kontsentratov v atmosfere vozdukha,
obogashchennogo kislorodom)
PERIODICAL: Izvestiya Vysshikh Uchebnykh Zavedeniy, Tsvetnaya..
Metallurgiya, 1958, Nr 6, pp 49 - 63 (USSR)
ABSTRACT: The object of the investigations described in the present
aper was to check the claims made by various workers
efs 1-5) who have stated that application of oxygen-
N
enriched air for roasting zinc concentrates can increase
the rate of oxidation, the degree of desulphurisation
and the concentration of B02 in the exhaust gases, although
this method of roasting when applied to lead concentrates,
which form easily fusible mixtures, miat cause diffi-
culties in obtaining a completely roasted and desulphurised
product. The experimental work was carried out in a
laboratory apparatus for autogenous down-draught blast-
roasting, shown in Figure 1, as follows: 1 - oxygen
Cardl/9 cylinder, 2 - pressure regulator, 3 - gas mixer provided
SOV/149-58-6-6/19
Roasting and Sintering of Zinc and Lead Concentrates in Oxygen-
enriched Air
with a propeller, 4 - sintering vessel measuring
20 x 20 cm and 50 cm high, with an effective hearth area
of 120 cm,21 5 - electric igniting device, 6 two
microgauges for measuring the flow of gases, dust
chamber, 8 - suction pump capable of drawing
150 m3 through 1 M2 of the hearth area per minute at the
maximum vacuum of 390 mm, H20 and 9 - electric motor.
The oxygen content (up to ?0%) of the gas mixture could
be controlled within + 21116 and was periodically checked by
chemical analysis of fhe mixture and by the manometer
readings. The quantity of air admitted to Vie gas mixer
was controlled by varying the vacuum under the hearth.
The weight of the charge varied between 14 and 30 kg.
Before each experiment the charge was moistened and then
carefully mixed. A small quantity of roasted agglomerate
placed on the grate served to support the charge, on top
of which 30 S of -coke and 200S of dry sawdustwem placed
card2/9. to facilitate ignition. Gas permeability of the charge
SOV149-58-6-6/19
Roasting and Sintering of Zinc and Lead Concentrates in Oxygen-
enriched Air
was determined by measuring the rate of flow of the gas
mixture on the entry side of the sintering vessel. The
temperature of the charge and of the exhaust gases and the
vacuum gauge and micro-manometer readings were recorded
at least once a minute throughout each experiment. In
each experiment three to twelve samples of the exhaust
gases were analysed for the C02 and oxygen contents. The
charge was made up to dry zinc concentrate - 40 mesh size
and partially roasted concentrate - 6 mesh size. The
compositions of the concentrate (top line) and the
partially roasted concentrate (bottom line) are given in
a table on p 51 (in the latter case both the total sulphur
content and the proportion of sulphur pfesent in the form
of sulphate are given). To obtain maximum gas permea-
bility, in the first series of experiments 8% of H20
was added to charge consisting of 85% calcine and 15%
concentrate. After each experiment, a sample of the
obtained calcine, crushed and screened through a 4 mm,
Card3/9 sieve was analysed for total sulphur content, sulphur
SW9'494'-6-6~P
Roasting and Sintering of Zinc and Lead o en ates Oxygen-
enriched Air
present as SO 41 total zinc and zinc soluble in a 10%
solution of H2804. In the first stage of the investi-
gation, the effect of the sulphur content of the charge,
consisting of 14.5 to 2% concentrate and 85.5 to 71-0%
calcine and forming a layer of 250 mm high, on the rate
Of roasting was studied. The results of some experiments
are given in Table 1 (top for air roasting, bottom for
roasting in oxygen-enriched air), and in Figures 2 and 3.
The time dependence of the basic parameters of the
sintering process in experiments Nr 63 (without added
oxygen) and Nr 58 (oxygen-enriched air) is shown in Figures
2 and 3, respectively. The scales of these diagrams (from
left to right) are w follow6: flowmeter readings in
mm H20; vacuum in mm H 20; the temperature of the
8xhaust gases in 0C; the temperature of the charge in
C. In the next series of experiments, in which the
sulphur content of the charge remained constant and equal
to 5% (corresponding to a content of concentrate of 15%),
Card4/9 the effect of the thickness of the layer of the charge and
SOV/149-58-6-6/19
Roasting and Sintering of Zinc and Lead Concentrates in Oxygen-
enriched Air
of the variation of the oxygen content of the gas mixture
were studied. The results of these experiments are given
in Table 2 (top part - variable thickness of the charge
layer, bottom part - variable oxygen content of the gas
mixture). In the next series of experimeAts, the effect
of the oxygen content in the gas mixtum and of the rate
of flow of the mixture was examined, the other conditions
being: the coiicentrate content of the charge - 13 to 15%;
the thickness of the charge layer - 350 mm in experiments
with air and 250 mm in experiments with oxygen/air mixture.
The data are given in Table 3.
The variation of the main parameters of the roasting
process during experiments Nrs 31 and 51 is shown in
Figures 4 and 5, respectively. The scales are the same as
those in Figures 2 and 3 with the exception that the curves
shown in Figure 4 do not include a graph of the variation
of the temperatare of the charge. The charge used in
experiments comprising the next stage of the investigation
consisted of 10 to 18% concentrate, 40 to 32% partially
Card5/9 roasted product and 50% calcine when roasting was done in
SOV/149-58-6-6/19
Roasting and Sintering of Zinc and Lead Concentrates in Oxygen-
enriched Air
air,and 10% concentrate, 40% partially roasted product,
and 5(r/o calcine when roasting in an air/oxygen mixture.
In both cases, 10 to 12% H 20 was added to the charge and
the thickness of the charge layer in all the experiments
was 200 mm. The results of these experiments are gi*ven
in Table 4.
Finally, roasting and sintering of lead concentrates were
studied, using both air, and air/oxygen mixture. Materials
used in these experiments included lead concentrate
containing 69.1% Pb, iron ore with 64.0% Pe, quartz with
94.?% SiO2 and limestone containing 50016 CaO. Roasting and
sintering were carried out in-two stages. The charge used
in the first stage consisted of: 100 kS concentrate,
14.? kS iron ore, 10.6 kg quartz, 13.7 limestone and 0 to
40% sintered agglomerate. The quantity of fluxesused was
calculated to give a slag containing 24% SiO, 2, 34% FeOj
16% CaO and 14% ZnO. The charge without the sintered
Card6/9 agglomerate contained 50% Pb, 11% S in the form of sulphide
OV/149-58-6-~/la
Roasting and Sintering of Zinc and Lead Mcentrates in Oxygen-
enriched Air
and ?% IL:,O. The charge used for the second roast consisted
of the piloduct of the first operation crushed to -6 mm
size and contained 4 to 6% moisturej The thickness of
the charge layer in the first and in the second stages of
the process was 200 and 300 to 325 mm, respectively. The
results of the experiments are given in T~ble 5.
It is stated in the conclusions that:
1) the results of acperi-ment on single-stage roasting
of zinc concentrate with recirculation of the calcine
carried out in air and air/oxygen mixture showed that,
other conditions being equal, the:mte of roasting and,
consequently, the output per unit hearth area increased
in proportion to the increasejpf. the oxygen content of the
air/gas mixture. Application of the air/oxygen mixture
increased the degree of desulphurisation of the concentrate
and correspondingly decreased the sulphur content of the
final product. Calcine was obtained under these conditions
which, even when the sulphur-rilch fines had not been
separated, contained as little as 0.12 to 0.4% S;
Card7/9 2) the higher the quantity of air or the air/oxyge'n
SOV/149-58-6-6/19
Roasting and Sintering of Zinc and Lead Concentrates in'Oxygen-
enriched Air
mixture blown through the charge per unit time, the higher
was the rate of roasting.
3) when the sulphur content of the charge roasted in air
exceeded 5 to 6%, the temperature 4ttained by the charge
during roasting and the rate of voqsting increased, a large
quantity of ZnO crystals was formed,.promature fusion of
the charge occurred and alcine with a high S content was
obtained. Although the oxidising reaction was even more
intensive when an air/oxygen mixture was used, the calcine
produced under these conditions had a low 8 content, did
not contain ZnO crystals and had good mechanical strength;
4) application of the air/oxygen mixture resulted in an
increase of the 802 content of the exhaust gases. (Better
utilisation of the oxygen could be obtained if the exhaust
gases with low contentration of SO were re-circulated.);
5) although the cadmium and lead ~Ontenba of the calcine
roasted in air/oxygen mixtures were very low owing to more
intensive volatilisation of these impurities, the losses
Card 8/9 of zinc under these conditions, due to volatilisation, did
1W..
SOV/149-58-6-6/19
Roasting and Sintering of Zinc and Lead Concentrates in Oxygen-
enmiched Air
not exceed 1 to 2016 and were not higher than those occurring
during roasting in air.
6) In comparison with two-stage roasting, the one-stage
process gives more uniformly roasted and sintered product,
increases the output of the hearth reckoned in wight of
ZnS treated per unit hearth area per unit time.
7) Application of air/oxygen mixture for roasting Pb-rich
concentrates did not increase the rate of burning owing to
the fact that these concentrates tend to fuse at com-
paratively low temperatures.
There are 5 figures, 5 tables and 11 references, 7 of
which are Soviet, 3 English and 1 German.
ASSOCIATION: Severokavkazskiy gornometallurgicheskiy intitut.
Kafedra metallurgii tyazhelykh tsvetnykh metallov
(North Caucasian Institute of Mining and Metallurgy.
Chair of Heavy Non-ferrous Metals)
SUBMITTED: June 9, 1958
Card 9/9
180) PM3Z I BOOK EXPLOrTATIOIN SOV/3199
Akademlya nak 3=. rnstitut obalichey I rworganlaheskoy khlmdi
in. X. 3. Xurnakova.
Analis blagarodnyth ustallov (Analysis or Noble Metals) Moscow,
1959- 193 P- Irrets. ally inserted. 2,700 copies printed.
Reno. 9d.s N. K. PshonItsyn. USSR Academy or sciences, Corm-
spandIng Member, and 0. Ye. ZryA&Int",, Doctor a.' Chemical
3olemeal &do. of Publiah-Ing Houses: T. 0 . Levi. and D. N.
TrIfonov; Tech. Ed.s 1. X. Ouseva.
PURPOUs Thin olleation of articles Is for scientists engaged
c
In the study
and analysis of the noble metals.
C0VXRA=t
& collection
afartlelos on the analysis of the
ThI
1m
:.
noble tat It includes Institute
Ltd me carried out by the
.
,
t
no and no Ch:
of 00 ria rgarLi c wintry La. X. 3. Xurnakov (AN SSSR),
" "It as reports presented by scientific research organizations
sad by Industrial enterprises at the Third " Pourth Conference
aim' him Metals hold in 1954 LPd 1957. respectively. -as
I
udl:sar4 reports describe now organic magenta rap griil--
t
Zrl oternInAtion of blatinum metals, and physicochandcal
thodt of MA17sis (Spec trophotom tr c, polarographLe and
I
tion
trIC). Special attention &
n
s given to spectral
Analysla for the determination of adalrtures In alloys of
i
platinum matals, Silver, and gold. an wrll as in refined noble
i
i
ma
o
1
he Collection also Includes analytical methods, tables
and ch&ftS for materials containing metals of the platinum
group, as well as a review of the literature on the analysis
of platinum metals published in the 1*st five years. No
personalities am mentioned. Rererencom roliow each chapter.
-Pabsoltsyn. N. K., I. V. PrOkOVYGY am
Use of Thiourea for the Concentration of Platinum Metals 15
FahenIts7n. N. K- and X- V- PQd0mnX*- Use of Nitrogen
--
-
rbazaa Acids for the Determi-
a
3mbstitutod 3&1t& of DI-EHro-c
23
nation of Platt - metals
Pahenitsyn. 1. K. 14. 1. Yus,ko and L. 0. SaljAkay-&-
Determination of iratrn-u-x-, In ReFlned
Silver 29
Panecitxyn. X. K. and 14. 1. Yuzlko. Spect-cphotametrIc
Determination or Rhoilum With the Aid or Potassium Iodide 37
r
p~h#nj.tAyn. X. K.jSg~~bu -and -
A~ i I
. n
. I. uric A
Dot r-Wnatlon or r1 us in i
Sp~:trophotow-rjo and Potontiometric Methods 48
_LL ~~~. Photaco2orLimetric Method for the
Determination of Rhodiue In the Presence of Platinum. 59
and T. P. Yufa. Phutacolorimetric Methods
l
n
G
-
th.-
. -6r-75-tlnum Metals
Anaiy to 65
d
r
.
PshonLtsyn. "IK K. A. Yeterakays. ard V. D. Ra,
-
Poiamgraphi. D~"rmdr=T6-n-6r-B1mv metal-~W=Fx
t%ares in
Refined Irldium TO
Mkirout B. A. (De6eased) and vV. D. Ratnikova. Datarxl-
*
1
. Yu.
Ined Silver B&rdLn
- . M. B.
--
.1
--
'
v and Anko. Pomrograph-la Determination
F i7i. ie;y
iTialko
of Certain Noble Metals br Using Platinum Zlectrvdas 80
Shulakov. V. M. )LlZAnghjjLpLk. V. M.
AnI
Z'..A.-J1e
~V
1
4
-
22" -arid Polarographlo
7
2f.cd, ror atIon of Copper, NIckol, Iron. Zinc
tormir
and L*sd by Using a Cationite In Products Containing Platlam
Metal* 88
18(6) PRAM I BOOK EXPLOITATION SOV/31S3
Akadeadys nauk SSSR. Institut obahchey I ~Organlch*skoy kbiall.
Is. X. S. Xurnakova
Analla b1WrOdnyft metallov (Analysis of Noble Metals) Moscow,
1959- 193 P- Zrrata slip Inserted. 2.700 copies printed.
Keep. Xd.s W. K. Pahanltsyn, UWR Academy of Sciences, Corre-
spondIng; Member; and 0. Ye. Zvyagint"v, Doctor of Chemlca~
and D. M.
Salencon; Ed~. of Publishing Housest T. 0 . Levi,
Trifonov; Tech. Id.s 1. M. Ouseva.
PURPOU, This collection of article, Is for scientists engaged
1A the study and Analysis Of the ft0bIQ metals.
a collection of articles an the analysim of the
CQV1]tAOZz
ThI
1*
sable tal In ludes studies Carried out by the Institute
:.
.
Y
=
Chemistry in. M. S. Xurnakov (AN =R),
of Oexhl and Inorg
as well an reporta presented by scientific research organizations
and by industrial enterprises at the Third and Fourth Conference
on'Noble Mot..;,.% held In 1954 and 1957, respectively. The
Itudi a and r*ports describe now organic Xrogent J- gr&,Tl--
: :
cc,,..c &I
.Irl: determination of blatinum =*team. ph'
methods of analysis (opectraphotometric, polaregraphic "
potentionstric). Special attention Is given to Ap"tral
analyst* for the dotorminatlan of &d=Jxzur*3 In alloys of
plat'num metals. silver, and gold, an wwLI as In refined noble
metals. The collection &Jac Includes ansaytical methods, tables
and charts for materials containing metals or the platlnum
group. as well " a review of the literature an tho snalyals
of platinum metals published In the last five years. No
29"Onalities am mentioned. References follow each chapter.
___
_?shemitsyn. N_ JL, 9. A. Qladyshovskay,& and I_ M. Ityakhova,
Use of the Zen Zxch&nV Method In the Analyst& of Platinum
Metals. Report 2. Separation or Rhodium from Irldlum 103
Yo. 1. Nlkltlna am V. N. Alyanch!kova.
nlutro-ns i~-b-t-arnng
1. Thos Cownt*d Substances for the Determination or
Platinum Metals by Spectral Analysis 115
.prap!y,JE._?. Spectral Method for the Determination of
FIXTIb' ralladlum, and Tellurium In S11ver-gold Alloys 128
and A. D. Qgtlka. Spectral Method of
Awaysio for Refined lriTrxWZ;d Ruthinitus 133
Aj S:OctrLl
=;g_8 A E_J"~ and Il- I
I. S~
cold y 139
'KurLmov, A. A Spectral Analysis or PliLtImin Alloys Con-
taining Three Comp2nents 143
Adakh k1 A P and V. K. Ur!cclin. D-terminirg the
1~ ~Nsla~owpos r. ~ or the Thermoelectric-
motive Fares 145
AT Zff*ot or Complo.stion and of the Acld-
the Potential of 'he
Au"/AuO, A."/A.0, Au""/Aut, and Agl/Ago Systems
_ 150
V. B. Kosova. Chromatometric Determination
Avilov,
of Gold 156
j. M. Qjonkov
and V. P-Watfill-
WAnL&ft
-
~
r the R --
kU t r
:
s
ctrometr zft.0 r0 minatIon of Silver in
3fl."r and Lead Alloys Containing Platinum Metals 163
and - - ChentmQva. Dissolving pl&t1hum
Their -j- %ne- Aid of an Alternating
-Current 1T6
Cbentsova, X. A., T. P. Yufa and - &avian. tic.
Method for the Analysis of palledt Liver Alloys 181
1uzhnIkO-- M. 5- and-1-1-Sheina. Methods of Testing
-
Palladium Alloys AM Thelr
Pro ~uc a on a Touchstone
And by Chemical Pken. 184
RO&MOV, P.I., lourest Stalinskoy premii, otv.red.; F.'MRIT51N, N.K.,
retsenzent; ZVYAGINTSEV, O.Ye., prof., doktor khim.nauk,
retsenzent; PRILSZHATEVA, N.A., prof., doktor fis.nauk, retgen-
zent; ANISI140-V,_ SM., prof., red.; smaov, r.G., red.; SEWOVA,
N.ya.#* A.D,, red.; DOLGIKH, V.I., red.; KAHAYEVA,
O.H., red.izd-va; ISIJW IYEVA, P.G.# tekhn.rad.
(Methods of analyzing platinum metals) Metody analize platinovykh
metalloy. zolota i serebra; abornik nauchnykh trudov. Moskva,
Gos.nauchno-tekhn.izd-vo lit-ry po chernoi i tovetnoi metallurgii,
1960. 256 p. (MIRA 13:9)
1. Russia (1917- R.S.F.S.R.) Krasnoyarskiy ekonomicheakiy admi-
nistrativnyy rayon. Sovat narodnogo khozyaystva. 2. Chlon-kor-
respondent AN SSSR (for Pahonitsyn).
(Platinum--Analysis) (Gold--Analysis)
(Silver--Analysis)
__Mj~_k~RV, S.M.,-_OREKHOV, M.A.
Dzying granulated concentrates and sinter cake by the suction
of preheated air. Izv.vys.ucheb.zav.; tsvet.met. 3 no.2:74-79
160. (MIRA 15:4)
1. Severokavkazskiy gornometallurgichoakiy institut, kafedra
metallurgii tyazholykh metallov.
(Ore dressing) (Sintering)
SMIZOVO Z.A.;
Alimli-sulfide method for the treatment of flue dust in lead
refineries. Izv. vys. acheb. sav.; tevet. met, 3 no. 6:65-73
16o. (MIRA 14;1)
I.EAv#eroiavkax~kty gornometallurgicheekty institut. Kafedra
metallurgit blagorodnykh i redkikh metallov.
(Lead--Ketallurgy) (Fly ash)
S1149A 1/000/001/006/013
A006/A(>Ol
AWHORS Anj_~~JToV M.,.Sav.1'skiy, S.L., Oaipov, A.P.
, 5_
T=- The Separation of Selenium and Tellurium From Platinum Metals in
the Form of Trivalent Ferric Salenite and Tellurite
PERIODICALi Izvestiya vysshikh uchebnykh zavedenly, Tsvetnaya metallurgiya,
1961, No. 1, pp. 101 - 105
TEXT: A method for the separation cf selenium and tellurium from platinum
metals used in analytical practice is based on their joint precipitation with fer-
ric hydroxide (Ref. 1). This method was tested and described by M.F. Proshkovich
and P.V. Faleyev (Ref. 2). The control of the full separation of selenium and
tellurium from platinum metals would be facilitated and simplified, if there were
data avallable on the solubility of trivalent ferric selenites and tellurites in
hydrochloric acid solutions at different aciditiea and temperatures, and on the
effect of ammonium ahlorides on their solubility. If In hydrochloric acid solu-
tions, containing tetravalent tellurium and trivalent Iron, the amount of the lat-
ter is not sufficient to form ferric tellurite, tellurium dioxide may be precipi-
tated If the solutions are neutralized. To bring about tellurium separation in
Card 1/4
8/14q/61/000/OOi/006/b13
A0061AOOI
The Separation of Selenium. and Tellurium From Platinum Metals in the Form of Tri-
valent Ferric Selenite and Tellurite
the form of dioxide, the optimum pH value must be known at which its speeded up
precipitation and the effect of ammonium chloride take place. Eventually, to ob-
tain ferric selenite and tellurite precipitates, enriched with selenium and tel-
lur.lum, the pH values must be selected, at which not only the coprecipitation of
platinum metals but also that of some impurities (iron) can be prevented. The
aforementioned problems were studied by the authors with the participation of
Engineer K.S. Perel'muter. Ferric selenite was prepared by the interaction of
ferric sulfate and sodium selenite by a method given in Reference 3, according to
which the precipitate has B. constant composition with a Fe-Se molar ratio corres-
ponding to Fe2(Seo3)3, The composition of the dry precipitate of Fe selenite ob-
tained is expressed by the formulae Fe2(SeO )/ 3H20- Ferric tellurite was pre-
pared by the interaction of 0.1 n. solution3o? podium tellurite (pH 1.1) with
0.3 n. solution of ferric sulfate. The molar Fe:Te ratio exceeded 2 3 times the
stoichiometric ratio of these elements in the formula Fe2(TeO,3 . The composition
of the dry precipitate Is expressed by the formula Fe2(TeO3) . to, The solubili-
ty of selenite and tellurite of trivalent iron was studied at 19, 40 and 700C in
hydrochloric acid solutions with pH - 1; 1.5; 2.0 and 2.5 and also in 11C1 solu-
Card 2/4
S/149/6i/"/00j/006/oj3
A0061P.001
The Separation of Selenium and Tellurium From Platinum Metal,-, in the Form of Tri-
valent Ferric Selenite and Tellurite
tion,~ containing 10% NH4Cl with p1H = 1 and 2.5, at 190C. It was found that the
solubility of ferric tellurites and selenites decreased with a lower acIdity of
the solutions; it was higher In HCI solutions with 10% ammonium chlorides. At
elevated temperatures in HCI solutions with pH - 1, a slight increase of trivalent
ferric selenite and tellurite solubility takes place. In saturated solutions with
pH 1.5, 2.0 and 2.5, the Te, Se : Fe ratio increases. To investigate the stabili-
ty of HC1 solutions of tetravalent tellurium, two initial solutions were prepared
by dissolving ~e02 in HC1. The former had a pil value of 0.85 and contained 0.98
mg/ml Te; the latter contained 2 mg/ml Te and 50 9/1 MVI with a pH value equal
to 0.5. It was found that the precipitation of tellurium dioxide from HCl solu-
tions of tetravalent tellurium proceeded already at a pH value of 0.5 and attained
a maximum rate at PH - 5.3 - 5.4. The precipitation of tellurites and selenites
of trivalent iron from HC1 solutions containing free HU, NP4C1 and ammoniates
of platinum, palladium rhodium, ruthenium, iridium was inve5t!gated at t-heir neu-
tralization with soda. The initial solution was composed of Se - 665; Te - 766;
Fe - 708; Pd - 69; Pt - 40; Re - 50; Ru - 30, and Ir - 30 (mg/1). The results
Card 3/4
S/-.4q/61/)00/O01/006/013
A006/AO01
The Separation of Selenium and Tellurium From Platinum Metals in the Form of Tri-
valent Ferric Selenite and Tellurite
obtained show that optimum conditions for the precipitation of tellurites and
selenite are pH values of 2.3 - 2.5 and a 90% excess of iron againsi the stoichio-
metric amount. Under these conditions tellurium extraction attained 97.5% and
selenium extraction 95.4%. The ferric selenite and tellurite precipitates separat-
ed out of solutions, at a pli value of 2 28, contained 215 g/t platinum, 460 g/t
palladium, and 59 g/t rhodium or 3.7; 4.6 and 5.1% respectively of their content
in the initial solution. The precipitate contained very small amounts of ruthenium
and iridium. There are 2 tables and 6 Sov!et references.
ASSOCIATIONS: Severokavkazskiy gornometallurgicheskly institut (North Caucasian
Institute of Mining and Metallurgy); Kafedra metallurgii tyazbelykh
tsvetnykh metallov (Department of Metallurgy of Heavy Non-Ferrous
Metals)
SUBMITTED- -juiy 4, ig6o
Card 4/4
ANISIMOV, S.M.; NEKRASOV, B.D.; PETRENKO, V.I.
Stage flotation of unyielding gold-bearing ores. Izv. vys. ucheb.
zav.; tsvet. met. 5 no.2:50-55 '62. (MIRA 150)
1. Severokavkazskiy Fornometallorgicheskly institut, kafectra
metallurgii redkikh i blagorodnykh metallov.
(Gold ores) (Flotation)
AN ..;_: l',M?NKO, M.
and separat.lon of impurities during Uin tbermal
dissociation of stlver nitrate. Izv. vys. uOheb. zav.-, tevet.
mot. 8 no.5.-61-65 165. (MIRA
1. Si-vvrc-k&vkn,.9kl.y gornometallurgichodkly instAtut, klifedra
metailluri-,li hlagorodnykh I rodkikh metallov.
ANISlMOV, S.M.; SVISTUNOV, N.V.; ASTAKHOVA, Ye.P.
Gold flotation out of pure quartz placer ores. TSvet. met. 38
no.11:45-50 N 165. (MIRA 18:11)
AIrriT71,37, 3. :,.
1 .1
v , ru~~r
Anisirnov, S. 14. "A rot,ol, ,or a nr,,,,- ,,-1
ill-Ul Im. K:11.111hj) I'Ali No. 3, ;-). 2P-~'.
A f
SO: U-3736.1 21 lvlay 53, (Lotopi.3 'Zhurnal Iiiykh 3tatey, Nlo. 1:~, 1)4)).
ANISIMOV, S.S Insh.s, DARAGAII-BUBHGHOV, V.L. in2h.
New pudiometers. Bezop. truda v prom. 2 no.11925-27 N 158. (HOA 11:11)
(Mudiometer) (Ultrationic waven-Industrial applications)
88715
S/127/60/000/OL-)6/007/007
0 B012/BO54
AUTHORS: lk~ ~Bilnov~,S- ~S-l and Daragan-Sushchov, V. I.
TITLE: New Method of Determining Atmospheric Pollution With Dust
PERIODICAL: Gornyy zhurnal, 1960, No. 6y P. 74
TEXT: From 1957 - 1959, the Tsentrallnaya nauchno-issledovatellskaya
laboratoriya. (TsNIL) Gosgorteldinadzora (Central Scientific Research
Laboratory (TsNIL) of the Gosgortekhnadzor) developed a dust counter which
is based on the capability of the acoustic field of changing its parameters;
in dependence on the chan,;e of physical constants of the air investigat---
An acoustic field is formed in the production of elastic vibrations by "'
respective sound or ultrasound vibrator in the direction of the analo-C111-
receiver in the gas medium investigated. If the distance between vibrator
and receiver is equal to X/2 (half wave) or its multiple, a "standing
wave" is formed. This state is caused by the physical atmosphuric state,
the frequency of elastic vibrations, the distance between vibrator and
receiver, and corresponds to the maximum enerEy output on the receiver
Card 1/3
'18715
New Method of Determining Atmospheric S/117/60/000/006/007/007
Pollution With Dust B012/BO54
element. On the introduction of components changing the physical atmos-
pheric state (especially dust), the parameters of the standing wave are
redistributed, and less energy is put out on the receiver element. The
degree of disturbance) and thus the change in emf on the receiver, can be
expressed in mg/m3 on the dial of the indicator. Such a device (produced
at the TsNIL comprises an electronic vibrator (generatin& vibrations of
5 - 6 kc sec., an acoustic working chamber, an acoustic compensation
chamber to eliminate the effect of temperature chanCes) with transmitter-,
an electronic differential amplifier, an indicator, and a filter, The air-
intake system is equipped with a rubber balloon. The electronic part of
the device is composed of semiconductors~O_P-4 (OR-4) mercury oxide ele-
ments are used as feeding source. The device weighs about 1.5 - 2 kg. Its
sensitivity can be changed accordinC to the frequency used and the dis-
tance chosen. The smallest amount of dust measurable is 10 - 20 me/m3. After
appropriate reconstruction it would be possible to record the dust con-
tent continuously. Tests of the device in the dust plants of the Institut
gigiyeny truda i profzabolevaniy AIIN SSSR (Institute of Labor Hygiene and
Professional Diseases of the Academy of Medical Sciences USSR) showed the
Card 2/3
88715
New Method of Determining Atmospheric S/12 6o/ooo/oo6/007/007
Pollution With Dust BQ1 2Y13054
high sensitivity of the device. Work is being- done at present to simplify
the design, increase the dependability, and reduce the weit;ht of the
device.
ASSOCIATION: Tsentrallnaya nauclino-isaledovatellskaya laboratoriya,
Gosgortekhnadzora RSFSR (Central Scientific Research
Laboratory of the Gosgortekhnadzor RSFSR)
Card 313
87706
3/032/60/'026/012/011/036
24. 11 bb B0201,10r.6
AUTHORS: Daragan-Sushchov, V. I. and Anisimov, S. S.
TITLE: An Acoustic Method of Gas Analysis
PERIODICAL: Zavodskaya laboratoriya, 1960, Vol. 26, No. 12,
1368-1369
TEXT: From the various m9thods basing upon the measurement of acoustic
quantities, the authors chose the measurement of the change in the
propagation velocity of acoustic oscillations in aii~ under atmospheric
conditionslas depending on the change of the density of the gas-air medium
effected by various impurities (especially CH 4). The physical basis of
the method is the fact that the propagation rate of sound in a gas mixture
is between the respective rates in the pure gases. The velocity of sound
in a gas is expressed by the equation V = YFP7_07 I
where y is the ratio of the individual specific heats, p the gas pressure,
and 9 the density. With a sound source emitting sound waves in the direc-
Card 1/3,
tK-eprkse Sn3.3:u Is r -ec e I Ver
The device constructed consists of an oscillation transmitter an
of aco stic oscillations made of piezooerami0sr which are both located in
a 5 M chamber. BY means of an electron generator, a voltage having
a frequency of 165 kaps is applied to the transmitter. The electric signal
is transformed into elastic oscillations of the same frequency, which
cause an electric signal on the surfaoe of the receiver element; this
Card 2/3
87706
An Acoustic Method of Gas Analysis S/032/60/026/012/011/036
B020/BO56
tion of the surface of the receiver which is located at a distance d from
the sound generator, the relation t a d/V 1 holds for the time required
by the soun- to cover this distance, where V, is the propagation rate of
sound in the gas mixture. If another gas_is/used, the propagation rate
is V., and in that case the relation t. d V 2 holds for t2P and the
relation At - t 1 - t2 - d(1/V 1 -1/V 2) for the difference in time, where
the difference in time is expressed as the phase angle between the trans-
mitted and the received signal by the relation 9 - 2nfAt - 2nfd(1/V 1- 1/V 2)'
where f denotes the oscillation frequency. The method used for measuring
the phase shift is sensitive to small concentrations of the gas impurities.
The device constructed consists of an oscillation transmitter and a receiver
of aco stic oscillations made of piezoceramios, which are both located in
* 5 cO chamber. By means of an electron generator, a voltage having
* frequency of 165 kops is applied to the transmitter. The electric signal
is transformed into elastic oscillations of the same frequency, which
cause an electric signal on the surface of the receiver elementl this
Card 2/3
Mei
An Acoustic Method of Gas Analysis S103~~',-.10261012,10111036
B 0 2 0, '~, '~ r ,'~
signal is amplified and transmitted to an indicator. ;,t a distance of
A/2 between transmitter and receiver,'a standing wav'a is formed, whereby
the maximum e.m.f. on the surface of the receiver is generated. By chang-
ing the composition of the gas mixture, the density of the gas medium and
thus also the wave length is changed. This leads to a change in the signal
phase, and to a decrease of the energy in the rec~iveri. The scale may be
calibrated in percents of the measured gas. The block diagram of the ultra-
sonic gas analyzer is shown in the.figure. The electrical part of the de-
vice*consists of semiconductor triodes n6E5 (M) and is fed by the ele-
ments OP-4 (0R-4). Several variants of this device are described. There
is 1 figure.
ASSOCIATION: Tsentralinaya nauchno-issledovatel'skaya laboratoriya Gos-
gortekhnadzora RSFSR (Central Scientific Research Laboratory
of the State Technical Inspection of Mining of RSFSR)
Card 3/3
ANISIMOV, S.V. (Borisoglobsk)
'PracticalO problems Included in N.WbkIn's books of problems.
Hat. v shkole no.6:74-75 N-D '54. (KI-RA 7:11)
(Ftxbkin. Nikolai Alokeandrovich) (Geometry--Problems,
exercises, etc.)
GLAZKOV, Aleksandr Nikolayevich, inzh.; PARFENOV, Afamaiy Nikolayevich,
kand. tekbn. nauk; Prinimal uchastiye ANISIMOV, Sh-Xe., inzh.;
VRONSKIY, L.N., ved. red.; VORDNCVA, V.V., tekhn. red.
,[Electric equipment for petroleum and gas refineries)Elektro-
oborudovanie neftegazopererabatyvaiushchikh zavodov. ~bskva,
Gootoptekhizdat, 1962 . 343 p. (MIRA 16:1)
(Petrolewn refineries-Electric equipment)
(Automatic control)
AWISIKOV. V. (Borisoglebak).
Activities of the mathematical section of the Methodological Aasociation for
the schools of Borisoglebsk. Hat.v shkole no.5:87 S-0 153. (PI-RA 6:9)
(VAthemat ice-Study and teaching)