SCIENTIFIC ABSTRACT MOCANU, V. - MOCHALINA, I. G.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001134820010-1
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• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Sequence Number: 10
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

moulm, V.; STAISJ, S.
"AdvantaCes and disadvantages of suring coniferr, in ordinary and Lr; -,:i,:c
p. 26. (R.'ETIaTA PADURILOR. Vol. ~8, no. 12, Dec. 1953, aicure:,ti, Runania)
SO: ISDnthly List of East European Accessions, L. U.. Vol. 3, No. 1', April Uncl.

MDCANU, Vj CEORCESCU, C.
"Contritutions to the knowledge of diseases in forest cultivation. F. 23.
(REVISTA FADURILOP, Vol. 70, no. 1, Jan. 1955. Bucuresti, Rumania.)
SO: Month y List of Fast European Accessions, (EEAL), IL.
V01. 4, No. 5, 14AY 1955. Uncl.

IUWTA/Plmt Diseases. Diseases of Forest Species.
Abs Jour: Ber Zbur-Diol., Ho 5, 1958, x6ft.
Author : Georgescu, C.C.; Kocanu, Victoria; Orenski, St.
Inst : amanian
Title : The Flaea&= angustifolla tracheorqcosis Caused by the
Fusarium oxysporum Schlecht. var. orthoceras (App.
et Wr.) Bilai Comb. Nova.
Orig Pub: Dul. atiint. Acad. RPR. See. biol. so. stiinte agric.,
1956, 8, No 3, 697-707.
Abstract: The F. oxysporum was isolated in specimens of
E. angustifolia infected with tracheomycosis.
Observations were made of the growth of the bingus,
its morphological and physiological characteristics
in different, nutritive media, and the dynardsm of the
Card 1/2

me, C Iq AJ 010
RUMANU/Plant Physiology - Water Regime. 1-3
Abs J~ur : Ref Zhur - Biol., No 6, 1958, 24&1.
Author ; Georgescu S.S., Catrina I.
Tnst
Title On the Study of Normal and Pathological. Transpiration,
Withering, and Moisture in Shoots: cut from Healthy and
Damaged Black Fine.
Orig Pub Bul. shtiint. Acad. RPR. See. biol. ahi shtiintse agric.
1956, 8, No 4, 739-753
Abstract The objects of study were black pines of the Mecliash re-
gion fifty years old, 28-29 cm. in diameter and 13-14 m in
height. The variations in transpiration Intensit (by the
Huber-Ivanov method) were studied in shoots cut from heal-
thy and artificially danyt (mostly through boring) trees.
The curve of the daily course of transpiration inten ity
had at the end of the vegetation period only one maximun
between 12 noon and 3 p.m. Daring the withering of the cut
Card 1/2

RUMANIA/Disemses Plants Diseases of Forest Species. 0-2
Abe Jour : Ref Zhur DOI., Ito 7, 1958, 30185
Author ; Mocanu, Vitoria
Inst :
Title : Contribution to Poplar Black Hybrid Ebytopatholoey
6rig Pub : Rev. paddriloi, 1957, 710 No 1, 23-26.
Abstract : A description of a series of new myxomycetes (Macroph
penziGii Ferrarie, Fusicoccum aescull Corda, Diplodia
gongrogena Tema) which were discovered in 1954 on four
poplars in Rvznnime
Card 1/1

An a tt,,ick rm
r-,' ~)y t -- fr s- As,'m a' ~l
n 3 3,
'Ic:4 i Lnr~ -~ ril
r I ui Acri -il t.,~ -i i -il` 1:!` rt~
L.". 71) no. I,, June, 19"t-
7-ast Europe-in Acce,~7',ors Listy Litr,-,ry o" CrmCrcss, Vol.

V. - CATRIDA) 1.
Contributions to th, rtudy of I ~~-ddity of standlnF tir-!~Pr Of rertain
7'ISTIA PADITRILOfi. (Asoctata StUntil"Ica a Infjnerilor ri T,,0,,,.Lcierd1cr
lit, Ponvida rt !-Jrdst,(~rul ArOCIlItIll-I A ej Sill,' JOIJItAII-ji tj
Puntilia. VC1. '11, no. 9, Sept. IT'S
2y 1.1-,t of I-P~t !-Iuror*,an Acce.~:!icna (FIEP.1) Ir Vol ", 'in. 6, J ine 191.'9
'Jncl .

RUBTOV, S.; KOCANU, V.G.
Contributions to the knowledge of the ecology of Rumanian larches.
Studii cerc biol veget 12 no.1:121-134 160. (EFAI 10:1)
1. Comunicare prezenta de T.Bordeianu, membru corespondent al
Academiei Republicii Populare Romine.
(Rumania--Larch)

POPESCU-ZELEM, I*; FUIU* S.; KOCANUt V.
Contributions to the knowledge of the radial growth of low-ist
plantations during the period of vegetation. Studii cerc biol
veget 12 no.4:461-474 960. (EEAI 10:5)
1. Membru corespondent al Academiai R,P.R, (for Popescu-Zeletin).
(Locust (Tres))

POPESCU-ZELETIN, I.; MOCANU, V. C.; PUIU, S.
- - ----
Evolution of the trees defoliated by Lymntria. monacha L. Studii cerc
Mal veget 13 no.3:283-403 '61.
1. Membru. corespondent al Academiei R.P.R. (for Popeacu-Zeletin).

POPESCU-ZELETINO I.; MOGANU, V. G.; PUIU, S.
Structure and dynamics of the radial growth duri th vegetation
eriod of a population of Populua x suramericanalDre) Guinier
ov, Imarilandical). Studii carc biol veget 13 n0-4:477-506 161.
f
1. Membru corespondent al Academiel R.P.R.(for Popescu-Zeletin).

BINDIU, C.; DONITA, N.; TUTIRIARU, V.; MOCANUI_V-
Water economy of some plant associations on the Babadag Plateau,
Dobruja. Rev biol 7 no.3:325-348 162.
1. Biologisches Institut "Tr. Savulescull der Akademle der
RVR, laboratorium Mr Gaobotanik.

POPESCU-ZELETIII, I.; MOCANU, V. G.
Contributions to the ~mowledge of the growth conditions
in the most important forestry association of the Babadag
Plateau. Rev biol 7 no. 4: 513-536 162.
1. Institut fur Biologia "Tralan S'avules(U".
2. Korraspondierendes Mitg1led der AkademaP- der RVH
(for Popescu-Zeletin.

AUTHOR: Mocek JiMf, Ing. CZECH/34-59-5-5/19
TITLE: Desulphuring in a Basic Open-hearth Furnace
(odsV:enl' v zasadite Martinove peci)
PERIODICAL: Hutnicke' Listy, 1959, Nr 5, pp 405-409 (Czechoslovakia)
ABSTRACT: The author evaluates published experimental results from
the point of view of the basic conditions of desulphuriza-
tion. On the basis of literary data, in Fig 1 the
dependence is graphed ot the (S)/Ealratio on the content
of free N CaO" Two straight liness are drawn in the
diagram corresponding to 5 mol.% and 10 mol.% FeO
respectively. In the above ratio a expresses the
activity cf the sulphur which is dissSlved in the liauid
iron. Generally in the paper the author uses square
brackets for denoting elements or compounds which are
dissolved in the liquid iron a-nd round bracks for denoting
elements or compounds dissolved in the slag. In the view
of the author, in addition to the basicity, the fluidity
of the sla6s is an important factor for desulphurization.
~he influence of iron oxide in open-hearth furnace slags
Card V3 2.s negligible except for its effect as a fluxing medium.

CZECH/ 34- 59- 5- 5/19
Desulphuring in a Basic Open-hearth Furnace
172 analyses of the metal in the slag published in the
work of Harders et al. (Ref 13), P. Herasymenko and
G. E. Speight (Ref 11) 1 1. Bornakhiy (Ref 14) and
Ko F. Ludemann (Ref 153 we're evaluated on the basis of
theoretical views relating to the basic conditions of
des 1 hurization. For each specimen the value of the
Ur ratio was calculated from the respective
(S)/ a' 11
8 contgnt in the slag and the composition of the metal.
For calculating the active coefficients the results
published by J. Chipman and C. W. Sherman (Ref 16) and
0. Wagner (Ref 17) were applied. From the slag
composition the content (molar fraction) of free calcium
was calculated (N The results were divided into
three groups withotge iollowing contents of FeO:
4 to 6 mol.% 8 to 12 mol.% and over 12 mol.%. The
bath tompera;ure has not been considered. Results of
production heats in basic open-hearth furnaces produced
in the ZVIL Steelworks, Pilsen,were evaluated in the same
way. A total of sixteen heats were investigated, of
which six heats consisted of carbon steel, six heats
Gard 2/3 were pre-molten for subsequent use in the acidic furnace

Desulphuring in a Basic Open-hearth Furnace CZECH/34-59-5-5/19
and four produced in a basically lined electrical
furnace. The analytical and the calculated results
for three heats are entered in Table 1. In Figs 4,5 and
6 the progres is graphed of desulphurization for three
melts. The results obtained in these experiments are
also e t t e r e d i n t h a (S)/ La I diagram, Fig 1.
a
The desulphurization capacity in the furnace cannot
be intensified excessively without affecting other
optimum features and also the economy of the manufacture
and, therefore, the ZVIL Steelworks will have to pay
more attention to desulphuring prior to charging into
the furnace or desulphuring after tapping.
There are 6 figvras 1 table and 28 references 5 of
which are Czech, 4 aerman, 13 English, 4 Soviet, 2 French.
ASSOCIATION: Vzkumn~ z zkus'abnf Ustav 7,4vodu y.i.Lenina, 111zen'
(Research and Test Institute, V. 1. Lenin Works, Pile
SUBMITTED: February 7, 1959
Card 3/3

CZECliOSLOVAKIA/Hurmr, and Physiology (Norml and P-Ith, I pric-il).
PL)od Circulati,,zi. Ile!%rt
abs J,-ur. Ref Zhur-Tli,--l , N 17, 1958, 79541
Auth, r Mc:~cek, Jiri; Orei, Ja.,.
InGt
Title Electrccardi.,Deraphic -Lnd Vectorcardi,--leraphic Signs
,-,f Hypertmphy -f thL. Uft Ventricle Wit!,. Full 11~)ck.
of the Left Pedicle.
Ori~,- Pub: Vnitrni lekarstvi, 1957, 3, ?ic 8, 709-714
Abstract: A direct dependei4cu is shiwn betwet.:n the de,:me
,,f expansion of the left ventricle, deternined
roentgen graphically, and the electrocardioCraphic
siGma of hypertrophy of the left ventricle
Card 1/1
7 P

CZECHOSLOWJM/Human and lLniml (florml and "P-5
PaUlologicnl). Blood Ci "cilia ~ ion. The Heart.
Abs Jcur Ref Zhur - BiA., N,) U, 1958, 5o818
Author 14icok, Jiri; Orel, Jan
Iust
Title Chan,-,co (-f the Stunach Gradient at the Presence ~-,f a
Complete Bloch of the Left Pedicle of Tavar in *-~cardlai
Lifracts.
Orig Pub Vnitrni lekarstvi, 1957, 3, No 8, 715-723.
Abstract No abstract.
Card 1/1

CZECHOSLOVAKIA / Pharmacology, Toxicology. Cardio- V
vascular Drugs.
Abe Jour; Ref Zhur-Biol,, No 9, 1958$ 42400,
Author : Sel, B.1 _Mocek, J.; Orel, J.
Inst :Not
Title :Bigeminy Caused by Reserpine.
Orig Pub: Vnitzni lekarstvi, 1957, 3, No 8, 74o-744.
Abstract: A hypertensive patient was given 0.1 mg doses of
reserpine (1) 3 times daily. Within 12 days after
the beginning of the drug the patient reported to
the clinic in an excited state, complaining of
shortness of breath, a sensation of heart stand-
still and a tendency to fainting for the past few
days, The ECG revealed bigeminy, caused by ventri-
cular extra-systolies. One week after discontinu-
ation of I the bigeminy ceased, but within 5 days
Card 1/2
34

W,:z Z).
361-370

GECAVA
tror-arj-' ogra- t4, r: c:.a:.gpL: -If! ..~cT., extracti or in nomal
vn i tr r, i r ~,a pre a r, dr. iri Fo Icak
.13 LOM LO I Off i K:--L i. i, i '.a rn dr . o5ef' ",,"rejda,

MOCEK,. Jlri ; STFFFA, Milos, ml . ; DVORAK, Ivo
Path o I ogi ca I Find an a tcm~ ca. I a i3pecta r,f thp I schem I c c.%:-rj' ..c
puln In into rmed i v te cor on ii ry syn d rome. V% i trr, I I itk . I I
no. 12:1152-1157 D 1 65.
1. 11. vnitrni kllnlkfi lokarske fp-ku'ty tlr.!v(-rq' t JJ~
Purkyne v Brne (predrj(,st.n - prof. Dr. jirl Polcak, .

II.,2k 1. 11. , iIr. . ,(P - I(,, I!, w", , , 1 ~ "I i I.., I
I -,T-,~ -ti, . ." '. : , ., . : 1 .1 .., I-
, - - . -. . . . I .

~MEVMO-
Some experiences in the construction of forest roads. p. 226.
NAMDNI SUMAR. (Dmstvo sumars;dh inzenjera i tehnicara Bosne i Hercegovina)
Sarajevo,, Yugoslavia* Vol. 12, no. 4/6, Apr./June 1958.
McntW,y List of East ELLropean Accessions (EE&I) LC Vol. 9, no. 2, Feb. 190.
UhcI.

xQCEVIC' M.
Use of explosives in ttle c(-),,3trucLic)n ul" forest road + --174-
WARODINI 5UVdi. (Drustvo suniars~,.in inzeiije-ra i teri~,ic---ra Bosne i
Sarajevo, Yugosl;~via- Vol. 12, no. 4/6, Apr./June
Eonthly list of L,.ast 6-uropean Accessi--s L,; 7ol. 9, ao. -, :":,. 1-1,1~6-
Uncl.

KOBAKEIDZE, David Nesterovich; MOCRABELI, A.I.J, red.; IMIADZE,
L'Aih. 1.1-1. ~-'. I ~- I
K.1.1 red.iz,d-va,, BOV V E.B., tekhn. red.
(Structural charneteristica of Insect communities of some
natural zones of the Georgian S.3. It. ) Strukturnye onobtinno-
sti entomokompleksov nekotorykb landshaftnykh zon Gruzin-
skoi SSR. Tbilisi, lzd-vo AN Gruz.SSR. 1963. 90 p.
(MIRA 16:11)
(GeorgiR--Insect poptilptions)

MOCHACKI, Adam, inz.
Products of the Polfer Magnetic Materials Work. Wiad elektro-
tecbn 31 no. 5:119-121 My 163.

ZAGULYAYEV, A.K.; PAVLOVSKIY, Ye.N. , akaderrdk, otv. red. [deceased I ;
BYKHOVSKIY, B.Ye., akademik, red.; C-POMOV, !.M., red.;
,l
XOCHADSKIY~,. red.; MA:J.ATO, O.A., red.; 5n, EIZCV,
red.; SHTAKELIBERG, A.A., red.
[Voths and pyralids attacking grain and foodstuffs] Moli
i ognevki - vrediteli zerna i prodo,.,ollstvennykh zapasov.
Moskva, Nauka, 1965. 270 p. (V I i'LA 19 . I)

MOCHAIAVA, T. P.
"Scientific Conference of the Moscow Oblast' SclentiCic Research Tuberculosis
Institute," Problemy Tuberk., No.,', pp 81,82, 1954
Translation M-617, 7 JY1.v 1955

AID P - 2223
Subject USSR/Aeronautics
Card 1/1 Pub. 58 - 6/19
Author Komov, B., Mochalin, A. and Pransketis, A.
Title Gliders should be given to the primary organizations
Periodical: Kryl. rod., 5, 6-7, MY 1955
Abstract This article belongs to the series of answers to the
question "What kind of mass-produced glider Is needed?"
The authors give the characteristics of a glider which
they suggest should be given to all primary aviation
organizations. Gliders M-3, M-4, M-5, M-6, a glider
transport truck, and some names are mentioned. Photo.
Institution: (DOSAAF)
Submitted : No date

/),I , , I, i,! .i,) 0
KOI!CV,B.; KOCHALM.A.. lnstruktor-latchik-planerist; PRANSKMIS.A..
.... .-.. -_ -.
chlen byuro planernoy sektsiy
Let's give gliders to groups in primary organizations. Kryl. rod.
6 no.5:10-11 My '55. (MLRA 8:9)
1. Predsedatell planernoy sektait Utovskego aviatekhkluba (for
Kotov) (Gliders (Aeronautics))

I . I . -11 1. 1 .~ . .1 . )1 -1 1 '-, - - : -:.t '(71- ~- , I - - I- - -
- - ------
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Sci "ISSR. I..,! , I . , 1 !-~ i ~- , " I --I I - I
I - I

MOCHhLIN uj7aruncn -Alm
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OtIms CC #At wAG-trmufor =4ar c=UUgm of ;&"o wA thad..,
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card 1/5
VACh&Ua &.1, rM*JayiM DirwAls Dejtg~Aajtjoa far SGIVUC DM*n=IURI
U'rt-U-0 Of tA. Fe..b*U- Tn. Ifil

MDCHALIII. AA.
Use of the Dirac function to solve beat conductivity problems. Inxh.-
fis.zhur. no.5:76-83 K7 158. (MIRA 123-1)
1. Tekhnologichookly institut, g. Yaroslavl'.
Oloat-Conduction)

AUTROR: A 1 -'1/1 7U/51)/002/1 0/(.;l 31020
B 5/ BOO
1T L E The Joint bpe of the Dirac !,(-.ut%tion ;,xid the InLe, ral
;,;R 101) 1 CA L: Inzhenerno-fizicheckiy zhurral, 1959, Vol 2p Nr lo,
A .,,Ac;~ In the procent paper i:~ :JIown of vi:,in. thc DirLc
delta-function for the ,;oli-Aion of to be 'ncrfori,:ed in
connection vith Uiu c.t1mil: tion of heat conductivity -,-.ne,
diffit--ion into,,:ral trannforno for two-layer
media. In U-.is iwu,od, iiii'itdLu, intci_:r;,Ll trtmLifortis z,.ve v~-.0-6
For 0,c.- soluLion oi* prolilci :; com~ectc(', wit), bodio:~ of Ii. il.c(l
dimolmion,:,, 1311~
cowl.tion, whiclt ;~; vf., hr~(,Yi 6eri-ved on the of bo;,,,!(* y
i:.,-; 1~c iued ;.dv~mtat,~0 oil oly in
-301uLion of' 1'roblml;: 11i Lh I lo?,'.., t i (; ri.,..
-1 :~o %rf-I I : I) i te(! 1,o). Othur - ~0-1,-e ,~il 1ple, ric le,,~ of tlie v~ r 7
of :")hero). 'lleco " 1.0 /. OVj e,~
Card 1/2

Tho Joint Uso of the Dirac Enlimtion %nd tile
Into,!ral Trangforms
Inntittite., Cit.- nf
;W 17 ()/ ('1'0 1 ~C
BI 15/BCjO7
0
C'I.~ ~ "I,/,.

:2"4"S-100 I L
AUTHOR: Mochalin, A. I. 3/170/59/002/11/oie/024
BO14/BO14
TITLE: The Problem of )feat Conduction for an Infinite'~~nde~r-b
PERIODICAL: Inthenerno-fizicheekly zhurnal, 1959,Vol 2, Nr 11, pp 109-113 (USSR)
ABSTRACT: This article deals with the problem of heat conduction of an
infinite cylinder which contains a cylindrical beat source. The
boundary conditions are assumed to be inhomogeneous. The problem
is solved by ths applioation of the Dirac 6-function and the
int gral transformation@ suggested by the author in an earlier
pap:r (Ref 3). with the help of these transformations the author
deduces equation (6) from equation (1). The variable r to eltainat-
ed by means of a Hankel transformation, and equation (7) is obtain-
ed from equation (6). On the basis of a further Laplace trans-
formation and a formula by N. Ya. Sonin (Ref 4), equation (16)
is then obtained for the temperature curve. Equation (17)
describes the temperature curve for the case of continuous action
of the heat source. In conclusion, the general applicability
of the above-desoribed solution is outlined in a special note.
There are 4 Soviet references.
Card 1/2

68770
The Problem of Heat Conduction for an Infinite Cylinder S/170/59/002 '11/018/024
BO14/BO14
ASSOCIATION: Tekhnologicheskiy institut, g. Yaroslavl'
CTpatitute of Technology City of Yaroslavl')
I L---r,
Card 2/2

8`277
S/ 1 7C)/C',/0O4/OO1/C)1 '~/O?o
S;7 0 0 9,,P, IS-37),1103) B 0 10 / B 05
AUTHOR: -6 0i - i i 0 On I im
TITLE: Heatin6 of a Sphere by an Inotant~trenus 11,~at Source on the
Surface
PERIODICAL: Inzhenerno-fizicheskiy zhurnal, 1r)(1, Vil. 4, No.
pp. 124-126
TEXT: The temperature distribution in a sphere cf radius R is souCht,
when at the instant t = to a heat source acts with thc enerCy density 0
distributed over the spherical surface r 1ZR. The Dirac functi-r. per-mits
the description of instantaneous effects, and thus the solutijr. is ob-
t,,ined. The differential equation
9 + A
2 ) r (t
-t~ t - a" v n 0 1
4 4-,(r
+ Br - (r-R) t-t-) (6) is set ~jp, where A and B tre the enert;y
densities of heat sources assui.-ied to be in the center of the --phore and
Card 112

8 277
Heating of a Sphere by an InstantaneOUB
Heat Source on the Surface
on its surface. The solutions
U) t- to)
e sh V-sTa r
u(r,t) = -2Q
8;1 rr ii -as oh s/a R
e,- LtZ
ft-- (t-to) sh I SA r
U(r,t) = -2 - 1
a I rr ii ras sh (s/a R
T L)-
obtained.
S/1 70,j~ 1/()C)At/CC %'019/020
BO'?/BO')~
sh ~o/a (R-rl)ds 'r 4-r1
sh Vs/a (R-r)ds (r > r,
are
There are 12 Soviet references.
ASSOCIATIONi Tekhnologicheskiy institut, g. Yaroslavl' (Tecl.nolc)C~~cal
Institute, Yaroslavl')
SUBMITTED: February 23, 1960
Card 2/2

33626
S/17o/61/004/002/004/018
11,9000 B019/BO60
AUTHOR: Mochalin, A. 1.
TITLE: Heating of a Finite Cylinder by an Instantaneous Point
Source of Heat
PERIODICAL: Inzhenerno-fizicheakiy zhurnal, 1961, Vol. 4, No. 2,
pp. 44-51
TEXT: The heat source was assumed to be placed in the cylinder axis. As
in Refs. 6 and 7, the author used the Dirac function and suitable integral
transforms to solve the problem. Spatial variables, varying within finite
limits, were eliminated from the differential equation by using an
integral transform with infinite limits. In order that the boundary
conditions be satisfied additional terms were added to the right side of
the differential equation, which contained the Dirac function. The
application of this method to a two-dim6nsional problem is shown here.
In accordance with the earlier developed method, the author assumed
undefined heat sources with energy densities A(r), B(r), and C(-) on the
Card 1/4

58 6 2 6
Heating cf a Finite Cylinder by an 3/170/61/004/002/004/1018
Instantaneous Point Source of Heat B019/BO60
cylinder surfaces, and obtained the following differential equatior for
the problem studied here:
au/at - a 2u/ax2 + 1 a (r -LU) 6(x-F-)6(r)6(t-t A(r)6(x)6(t t
18 r ar ar 2nr 0
+ B(r)b(x-I)b(t-t0 ) + C(x)b(r-R)b(t.-t0 (4), where the following
boundary conditions hold:
[u(x,r,t)lx= = 0; u(x,r,t) 0; u(x,r,t 0, and the fcllcwlng
f 0 1 ix-1 = I )] r=R ~
initial conditions: lu(x,r,t)lto ~ 0. A Hankel transformation of zeroth
order and two Laplace transformations were applied to obtain an algebraic
equation, from whose solution the function u(X,rt) was determined. The
calculation of the integrals contained in this solution occup4es most
part of the paper. The following formula wan obtained for a solution:
Card 214

Heating of a Finite Cylinder by an
Instantaneous Point Source of Heat
AQ
8
X
4, r~e-
_Xp+ r2 (s+x),+ r,
V(2 al -. +,t:)'
.4- 1/-(2 w ++ x)-+-r'
Kv. (VTla V(2ni-s + x)2+rl)
4
1/ (2 nl-z+x)-t r2
r
(2
(V'~I-a V(2 zi+e-x)2+r2) (28)
Card 3/4 'V(2 n1 + z-xP+r--
88626
S/770/61/004/002/1004/011~
I/ B019/BO60
C10-f.) (IS, S,x
a
(V-stla I/ r2)

58626
Heating of a Finite Cylinder by an S/170/61/004/002/004/013
Instantaneous Point Source of Heat B019/BO60
Here, K1/2 is a modified Bessel function of second kind:
K1/2(v) = K-1/2(v) - fn/2v e-v . There are 10 Soviet references.
ASSOCIATION: Tekhnologicheskiy institut, g. Yaroslavl, (Institute of
Technology, Yaroslavl')
SUBMITTED: April 6, 1960
Card 4/4

MCLUCHER. Vallter [Hollitacher, Walter]; AKQWRIN, I.A. Etranslatorj;
ARMUGELISKIT, U.S. (translator]; Y~~L ~&_Ajj,_(~ranslatorj;
ORMITAMOVSKIT. H.S., akedemik. red.; OPARIN, A.I., Omdenik, red.;
KAMICH. A.G., doktor fiziko-matem.nauk. red.; OVCHIHUIKOV, N.Y..
kand.filosof.nauk. rod.; TYURYUKANOV, A.N., kand.biolog.nouk., red.;
GALIPMRIN, Pja., doteent. red.; URYSOH, K.I., ksnd.biolog.nauk,
red.; MAKAROV, A.A.. red.izd-ve; ZMOVA. N.V., tekhn.red.
(Nature in the scientific picture of the world] Pr1roda v aDuchnoi
kartine mire. Obahchaia red. i vatupitelinnia statlia K.E.
Omellinnovakogo. Hoakva. Izd-vo inootr.lit-ry, 1960. 469 p.
(KIRA 14:))
1. AN USSR (for Omellyanovskly).
(Science--Philosophy)

MOCHALIN, M. P.
MOCHALIN, M. P.: "Hathods of increasing the effectiveness of horizontal
de*livery of mined material in working large deposits of hard ores".
Moscow, 1955- Inst of Mining$ Acad Sci USSR. (Dissertation for the
Degree of Candidate Of TECIMICAL Sciences)
SO: Knizhnaya Letopis' No. 51, 10 December 1955

KOCHALIN. M.P.
Ore transportation on scraper levels and ways to impr07e it. TrIX17
Inst.gor.dela no.2:26-)l '55. (KLRA 9:))
(Kiaing machinery)

GUL V.11.; BilElIDAROViCII, DACK. , brigudir sharoahechnoeo bureniya
(Sokol'nyy ruAnik); BEOTOV, ?.Ye.; DZIflWARDZHlDZZ, U.K.;
KOCdALIII, X.P. - PRIGOVIN, Te. 1. , gornyy Inzhener (Metallichs-
FOLISHCOX. A.D.
Speeches by participants in a conference. Gor.zhur. no.1:20-24
Ja '56. 04LRA 9:5)
1. Nachal'nik Proizvodstveano-tekhnicheskogo otdela Dzhezkazgan-
skogo rudoupravlaniya (for Dzhemardzhidze); 2. Nauchnyy sotrudnik
lustituta gornogo dela AN SSSR (for Mochalin); 3. Glavnyy
inzhener Ukrglavrudy (for Follshchuk); 4. Glavayy Inzhener
Bystrushinskago rudaika (for Guliy); 5. Glavayy Inzhener Salair-
skogo rudnika (for Baketov).
(Mining engineering) (Mining machinery)

r I ~ (-: c H #~ k 1, t\, , / I ~ i-f,,
NOBANHIME. V.D.. Cornyy inzhener; MOCHALIE M.P.. frandidat tokhalchaskilda nauk.
Ore deliveries direct-,y from the stoue. Gorabur. no.9:12-14 5 157.
(Ore handlirz) (Mining engineering-Sefoty mosswes)

AGOSHKOT, Mikhail Ivaaovlch; KQCHALIN, Mikhail PantalWonovich. kand.
takhn.na-n ; ISLARKINA, T.F., red.; SA-V-66i~;' Ye-.-T.-,-fekhn. red.
Nechanization of underground ore mining] Kakhanizataiia
podze=oi dobychi rud. Moskva, Izd-vo OZnanie.0 1958. 44 p.
(Vsaaoiuznoe obahchestvo po rasprostranenliu politicheakikh i
nauchnykh znanii. Ser. 4, no-36) (MIRA 12:7)
1. Chlon-korrespondent AN SSSR (for Agoshkov).
(Mining machinery)

fi Z_ / A/ 197 - 1e'
Problems in the Exploitation
of Mineral Ore Depoeitfi, lzd-,,r(;, Ali F3657,,
Golushkevich with reference to statically determined masses. A
practical case is considered to illustrate the hiatus between
empirical formulas and well-developed theories. There are 27
figures, 2 tables, and 19 references of which 13 are Soviet, 4
German, I Rumanian, and I Hungarian.
PART II. SUBSURFACE EXPLOITATION OF MINERAL DEPOSITS
_Aaashkov,, M.I., Corresponding Member of the Academy of Sciences, USSR.
and Mochalin, M.P., Candidate of Technical Sciences. The affect of
Brokin__0__r_e_S_fze___6n the Rate of Output 73
In mining hard ores the productivity of a mine can be considerably
increased by the efficiency of drilling and blasting operations.
To reach high production levels the problems of haulage and hoist-
ing must be satisfactorily solved. Scraping time, idling, second-
ary crushing, the effect of the size of broken rock on the effi-
ciency of transportation, etc. are analytically examined. There
are 6 figures and 7 bibliographic references,of which 6 are Soviet

AGOSHKOV, R.I.; BROITNIKOV. D.H.; KOVAZHF21KOV. A.V. (deceased]; NIKMOROV,
V.I.; MOCULALIN. K.P.; VCRONM . A.S.,i Prinimali uchastiye: E3ASA-
VIN, G.A.; GAGULIN. H.V.; BA3SNOV. F.A.. T33POWSOT, Z.A.. L-a--A.
takhn.nauk, otv.red.; IIIKOLAT3VA, I.N., red.izd-va: DOROKHINA.
I.M., tekhn.red.
EInvestigating the main technological processes of underground
mining of thick hard ore deposits] Insledovanie o9novnykh
takhnologichaskilch proteessov pri podzemnoi razrabotka moshchnykh
mostorozhdonii krepkikh rud. Moskva. Izd-vo Aked.nauk SSSR, 1959.
359 P. (HIRA 13:2)
1. Chlen-korrespondent AN SSSR (for Agoshkov).
(Hining engineering) (Ore dreBsing)

-- MAT-M, Mikhai.I-Pan:teIaY=aQvicb; ZVEKOVP Vladimir Afanastyevich;
AGOSHKOVO M.I.0 nauchnyy red.; ASTAKHOV, A.V.,, red. izd-va;
BOLDYREVA, Z.A., takhn. red.
(Self-propelled equipment in mines] samokhodnoe oborudovanie na
rudnikakh. Pod nauchn. red. R.I.Agoshkova. Moskva, Gos.nauchno-
tekhn.izd-vo lit-ry Po gornowu delul 1961. 391 p. (MTLRA 14:12)
1. Chlen-korrespondent AV S= (for Agoshkov).
Nining machinery)

MCClUtLIN, M.P., kand.tekhn.nauk; MARSHEV, A.S., inzh.; YAKOVLEV, V.G., inzh.
SBU-Z and SBu-4 self-propelled drjUing ri.:73. Gor. zhur.
no.6:56-58 Je 162. (MIRA 15:11)
1. Institut gornogo dela im. Skochinskogo (for Moch&lin).
2. TSentraltnyy nauchno-issladovatellskiy i proyektno-
konstruktorskiy inatitut podzemnogo shakhtnogo stroitellstva,
I-'Loskva (for Marshev, Yakovlev).
(Boring machinery)

MOCULINj M.P., karid. tekhn. raquk
Mechanizat', -;n of' I I rip ri~ b.- t t_ 4
.% *-, , r.
- I I I I.. .
01',4 dfpns I t ning. C,()r. z, ir. 3--3~, ~ d, :
11 ',rL-3t,tut ~,!' ri 471. .x0, ;~-(, -
1 1 4.., ".- - " I ll~- t,~ Ir( .

AUTHORSt Nazaroy, 1. 11. Member, Academy of Sciences, 2o-124-4-32/63
USSR, Gusey, B. F., MA-in, 3, M., Mochalin, V. b., Nazarova,
1.1., Vinogradov, V. P,, Kruptsov,-B7-,",-,-Shiyrygina, 0 A.,
Nazarova, D. V~
TITLE, The Condensation of Acetylene With Methylheptanone and Its
Analogues (Kondensatsiya atsetilena s metilgeptanonom i yego
analogami) The Synthesis of Linalool and Its Analogues (Sintez
linaloole i yago analogov)
PERIODICAL: Doklady Akademii Nauk 33SR, 1957, vol. 114, Nr 4, pp 796-799
(USSR)
LBSTRACTo Several years ago a simple method of synthesis of different
acetylene alcohols was worked out in the laboratory of the
authors by means of condensation of aldehydes and ketones un-
der the influence of powdery caustic potash with acetylene at
high pressure (5-1o at superpressure). It was of interest to
employ this method in the condensation of acetylene with methy)-
heptanone and simihrketones, in order to obtain the correspond-
ing acetylonealcohols. Linalool and some analogues may then be
obtained easily by partial hydrogenation with a Pd-oataly8t.
Hitherto such condensations have usually been carried out under
Card 1/4 the influence of metallic sodium in a soiution of liquid ammonia.

The Condensation of Acetylene With Methylheptanone and Its 2o 1-,4-4-32/63
Analogues. The Synthesis of Linalool and Its Analogues
It was found that methylheptanone and its various ane1ogues
may be condensed very easily with caustic potash and acetyl-
ene at the above-mentioned pressure. At o-2oOC they give as a
result the corresponding tertiary acetylene alcohols with an
almost quantitative yield (more than qo~), This reaction may
also be carried out without acetylene pressure, however, some-
what more slowly and with a yield of only 6o-8o%. It has been
previously shown in the same laboratory that acetylene alco-
hols which contain a non-subatituted acetylenehydrogen may be
hydrated highly selectively in the presence of palladium over
calcium carbonate or copper coated zinc powder, Thereby
vinylalcohols with an almost theoretical yield are obtained.
The acetylene alcohols mV not be selectively hydrated with
other catalyuts (Ni, Pt) and are therefore useless in the pro-
duction of pure vinyl alcohols. An analogous picture may also
be noticed with the hydrogenation of the above-described ace-
tylene alcohols which are obtained by condensation of acety-
lene with methyllieplanone and its analogues, These acetylene
alcohols may also be highly selectively hydrated in the pre-
Card 2A sanoe of a Pd-catalyst. They form linalool and its analogues

The Condensation of Acetylene With Methylheptanone and Its 2Q -114-4-32/63
Analogues. The Synthesis of Linalool and Its Analogues
with an almost theoretical yield. The purity control of the
vinylalcohols (linalool &nd its analogues) was carried out
by means of the acetylene test (with ammonia solution of
silver or copper oxide), whose sensitiveness was determined
by special tests and amounted to 0,2-0,3%. At the hydrogena-
tion of the acetylene alcohols with a Pd-catalyst the acety-
lene test always disappears at the theoretical point, that is,
as only one hydrogen molecule is strongly attached. The acety-
lene alcohols obtained in the course of this work are summe-
rized in table 1. Linalool and its analogues (table 2) were
obtained by a partial hydrogenation of the above-mentioned
acetylene alcohols with Pd-cat%lysts. In the experimental part
the methods and yields of the said substances are described in
detail. There are 2 tables and 5 references, 3 of which are
Soviet.
ASSOCIATIONt Institute for Organic Chemistry imeni !J.D. Zelinakiy of the All
USSR and Moscow Institute for Refined Chemical Technology imeni
M.V. Lomonosoy (Institut organicheskoy khimii im. V.D. Zelins-
Card 3/4 kogo Akademii nauk SSSR i MoskovakiY inatitut tonkoy khimiches-

The Condensation of Acetylene Nith !Aethylheptanone and Its 1 114-4-32/63
4nalogues. The Synthesis of Linalool and Its Analogues
koy tekhnologii im. M.V. Lomonosova)
SUBUITTEDs March 12, 1957
Card 4/4

AUTHORS Nazarov, I. N., Academician, Makin, S. Y., 20-114-6-29/54
Mochalin, V. B., Nazarovaq D, V., Vinogradc.v, V. P.,
_rri-uptaov, f~. K. . Nazarova 1. 1. and Shav-rygina, 0. A.
TITLE: The Synthesis of Methylheptenone and Methylheptadienone
Analogues (Sintez analogov metilgeptenona i metilgeptadiyenona)
PERIODICAL: Doklady AN SSSR, 1957, Vol. 114, Nr 6, pp. 1242-1245 (USSR)
ABSTRACT: This synthesis is of interest for the production of a
number of corresponding analogues of natural isoprenoid
compounds. The initial acetylene-alcohols for this purpose
were produced according to the authors' method (reference 1).
By a selective hydrogenation in the presence of palladium
on calcium-carbonate acetylene alcohols are almost
quantitatively converted to analogous vinyl alcohols
(reference 2). These latter yield the corresponding
analogues of methylheptenone in three different ways
(reference 3). Method A. By the influence of gaseous
hydrogen chloride or hydrogen bromide upon tertiary vinyl
alcohols at 0 - 2o 0C primary haloid-derivatives of an allyl-
-type easil~r form (reference 4). Their condensation with
Card 1/3 sodium-acetate-acetic-ether with a subsequent saponification

The Synthesis of Nethylheptenone and Methylheptadienone 20-1-14-.6-29/54
Analogues
leage to methylheptenone analogues. Method B. At 14o -
19o C tertiary vinyl alcohols directly react with the same
ether. An almost theoretical quantity of ethanol and CO 2 is
separated and the same analogues as in A) are obtained.
Method V. By the action of diketene upon tertiary vinyl
alcohoFs' in the presence of small amounts of triethylamine
or piperidine, acetonacetic ethers of these alcohols are
obtained (table 2). Their pyrolysis also leads to the above-
-mentioned analogues (reference 6). The 293-dimethyl-2-
-heptene-6-on (IV) necessary for the synthesis of irone was
produced all three ways mentioned. Dimethylisopropenyl-
carbinol (initial substance) was produced by the influence
of methyl-lithium upon methyl-metacrylate. All methyl-
heptenone analogues produced are comprised in table 1. The
authors further produced: allyl- (I) (reference 9), crotyl-
(II) and chlorocrotyl-acetone (III) (reference 8), dimethyl-
isopropenyl-carbinol-acetoacetate, dimethylheptenone (IV),
cyclohexylidenpentanone (IX) and tertiary butylheptadienone
(XIII). The production methods and constants of these
substances are given. There are 2 tables and 12 references,
Card 2/3 6 of which are Slavic.

1.1ficHAlillp V. B.: 14710ter Chrm Scl -- "jnlr.~c3tlq,-t+,'rjn (11' li.r. ri r~nl
I I I " r. . . : J,, , (,
cyclization of compouryla". moncow, 1% -In (:-1' 77 : _,' ..- ~- 7 - =,, ,
Monc ow Iri,~it of Finr, Ch,,m 7echnol( ir,.' I m V. Tj-,-i(,r,(,f3(jv) , 'I '(~ , (I ',T(. i. ,
I ~Tp
I)Dr), 122)

5 (3) SOV/79-.'9-3-4/61
AUTHORS: Nazarov, I. N. (Deceased), Makin, S. m., Yochalin B.,
Shavrygina , 0. A., Nazarova, D. V., Kruptsov, B. K.
TITLE: Synthesis of Analogues of Geranyl Acetone and Pseudoionone
(Sintez analogov geranilatsetona i psevdoionona)
PERIODICAL: Zhurnal obshchey khimii, 1959, Vol 29, Nr 3, PT, 744-753 (USSR)
ABSTRACT: These analogues are initial products for the synthesis of
the corresponding analogues of the most important natural
isoprenoid compounds, of vitamin A, carotene, farnesol, as
well as of phytol, a componont of vitamins K and E. Recently,
the authors reported on three synthores of ketones of tY,c
isoprenoid type carried out by them: 1) By reaction of E3o(,,,-'um
acetoacetic eater with halogen derivatives cl' the allyl type
(method A). 2) By reaction of vinyl- and ethynyl carbinols
with acetoacetic oster (method B). 3) 13y pyrolysi.,3 of the
acetoacetates of vinyl- and ethynyl carbinolz (method V',~.
This method was used to obtain methyl heptenone, methrl
heptadienone aid their analoMen (Refj 1, 2). By ~!on~enaation
of methyl heptenone and its analogueri with ace~jylene under
pressure (5-10 atmospheres excens preagure), dehydrolinalool
Card 1/3 and its analof?ues resultel almost quantitatively. These com-

SOV/79-2 9-
Synthesis of Analog-ues of Geranyl Acezone and Pneudoionone
pounds were transformed by partial hydrogenation over a
Pd-catalyst into linalool and its analogues (Ref 3). The
three methods used for the synthesis of the ketones of the
isoprenoid type were also employed for the synthesis of
various analogues of geranyl acetone (Scheme 1). The syn-.
thesized analogues of geranyl acetone are shoun in table 2.
The synthesis of the pseudoionone analogues was carried out
according to the methods D and V. In heating the analoju~s
of dehydrolinalool with acetoacetic eater the analogues of
pseudoionone were formed (Table 3) (Scheme 2), in yields
of 50-7e/o. The pyrolysis of acetoacetates of -the dehydro-
linaloola preponderantly leadc; to one of the poeudoionone
isomers; the other in obtained but in small quantition VhiC:1
is not the case with the paoudoionone analoC~ues "XVIII~ and
(XX), where two stereoisomeric forms (Table 3:1 were separate.'
in f02'M Of their hydrazonea. The compounds 3ynthesize,' are
characterized by absorption spectra in the ultraviolet range.
There are 3 tables and 7 references, 5 of which are Soviet.
ASSOCIATION: Mookovskiy inatitut tonkoy khimicheskoy tekhnologii
Card 2/3 (Moscow Institute of Fine Chemical Technology)

SCV/7 9- 2/~- 3 - 4,"61
Synthesis of Analogues of Geranyl Acetone and Pseudoionone
SUBMITTED: January 23, 1958
Card 3/3

VASILIRV, S.V.; MG~HALIN, V.B.; I-IKIIC),';111-',RSI'CV, V.11-1.
Ethers of substituted propa-rgyl alcohols. Part 2: --ffect f
subat-ituents in the alkylation reaction. Zhur. ot~. khim. 14
no.10:3180-3183 0 164.
; X -I RA 1 - : ~ i
1. Moskovskiy institut tonkoy khimicheskoy teklinologii im.
Lomonosova.

5 (,1)
AUTEORS; Yakin, S. M., Mochalin, V. B., 7IC7,!-7-~ 1-29,,177
Shavrygina, 0. A., Nazarova, D. V., Nazarov, I. N. ~Deceared)
TITLE: Synthesis of 1-h4n Analogs of Nerolidol, Farnesil Acetone -nd
Geranyl Linalool (Sintez analogov nerolidola, fnrnezilatsetana
i geranillinaloola)
PERIODICAL: Zhurnal obahchey khimii, 1959, Vol 29, Nr 4,
pp 1176-1182 (USSR)
ABSTRACT: In the present paper the authors investigated thoroughly
the synthesin *of isoprenoid alcohols and -ketones (of the
analogs of the above-mentioned products) and of the inter-
mediate products accirding to the given scheme. The
condensation of the analogs of geranyl acetone (a) with
acetylene was carried out in the steel reactor at 0-200 and
at 3-10 atmospheres exceos pressure in the presence of
poudery caustic potas'. The yield of tertiary acetylene
alcohols (b) was PO-85 '~42. The condensations hitherto useC,
(Refo 5, 6) are v,~rv nomplicated. All analogs of dehydro-
nerolidol (b) Gynthesized in this investigation are
presented in table 1. According to previous experiments
Card 1/3 (Ref 7) it whs possible to carry out the hydrogenation of the

C' nthesis of the Anrlogo -if ':,?rolilol, F-rnosil
OY
Acetono and Geranyl LinalA].
nc,?tylenn o~jtnined, th,~ of
(b), in the .-irr?oo-ncr of the -nalo.-'S -;f
norolLrlol (v) obt:-inl~~d b,, pnrti'Al hy,r-17CM,-'~i z- --'~,tylcne
-'Irohols (b) with this catalyst -.r- -ivcn in tblc- 2. Accor,!ing
to the reaction witli cntalyst3 f!,mcribed in reforcrce P, the
authors were able e,~xlicr to carry out the reaction of
terti,-ry vin,.-l -lcohols ---iith acotor~.cctic ester at 1,C-19c)
also without catalysts, anH obtnined in this methyl
heptene, geranyl ;,cetone, and their annlors (Ref., 1, 2). In
the present study they applied this method to tie nynthesi3
of the analogs of ff~rnesil acetone (g). 7hen heating the
nerolidol onalogs lescribed above (Table 2) with -cntoncetic
ester at 160-2000 the analogs of farnesil acetone (p,) were
obtained (Table 3). The analogs of farnesil rcetone (g)
synthesized vere then condensed with acetylene. The resultim:*
tertiary acetylene alcohols (d) were converted by partial
hydrogenation on Pd/CaCO, into the analogs of gerinyl linalo6l
W (Tables 4 and 5). The compounds obtained could be used in
Card 2/3 the sy-nthesis of the corresponding analogs, the Phytol, a

Synthesis of the Analogs of Nerolidol, Farnesil SOV/7SI-29-4-29/77
Acetone and Geranyl Linalobl
constituent of vitamins K and E. There 5 tables and
8 references, 6 of which are Soviet.
ASSOCIATICN: :,Ioskovskiy institut tonkoy khimicheskoy tekhnologii imeni
Lomonosova (Ifoscow Institute of Fine Chemical Technology
imeni Lamonosov)
SUBMITTED: March 28, 1956
Card 3/3

S/079/60/030/05/15/074
BOO5/BI26
AUTHORS% Makin, S. K., Mochalin, V. B. Nazarova, D. V.
TITLEt Ring Closure of inal'o'g's'of Pseudoiononeland Citrall
PERIODICALt Zhurnal obahchey khimii, 1960, Vol. 30, No. 5, PP- 1471-1476
TEXTt The authors examined the ring closure of five previously (Ref. 11)
synthesized analogs of pseudoionone with different gemrsubstituents in
position 1. The reaction scheme of this ring closure is given. The ring
closure was carried out with the help of two standard methodst 1) Ring
closure under the effect of boron trifluoride in a benzene solution at
-50. With this method the relevant a-ionone is produced. 2) Ring closure
by the effect of a mixture of concentrated sulfuric acid and acetic acid
at 10-150. A mixture of cc- and P-ionone is produced by this method. The
products were identified by the analysis of their ultraviolet absorption
spectra. Table I shows the results obtained by ring closure by method 1).
The analogs of pseudoionone with the following gem.-substituents R in
position I were examineds R - EI; C2a5; 'so-C3H7; tert '-C4E[9; Cl.. The
Card 1/3

Ring Closure of Analogs of Pseudoionone and 5/079/60/030/05/15/074
Citral B005/B126
above tablo above boiling range, refractive index, Amaze kmax , yield
and results of the C,H-determination for each of the products olgainsl_ty ring
closure. 2,4-dinitrophenylhydrazones were produced from the resulting
analogs of 0(-ionone. The table also gives melting point, n max. and
nitrogen content of these derivatives. Table 2 gives the results obtained
by ring closure by method 2). Both analogs of paeudoionone with the
substitu6nts R - H and R - C1 gave no ring closure by either method,
since the activating energy necessary to form the carbonium ion, which
is an important intermediate, is in both cases too high. The authors
also examined ring closure of some analogs of citral, which were previous-
ly (Ref. 13) synthesized. In this case ring closure was brought about by
the effect of sulfuric acid on the Schiff's base of the citral analog
(Ref. 14). Mixtures of o(- and 0-cyclocitral were thus formed; the re-
action scheme is given. The analog with R - H gave no ring closure here
either, while the Schiff's base of the compound with R - Cl split off
under the effect of sulfuric acid HC1, and changed into a cyclic product,
whose structure was notdetermined. Table 3 gives the results obtained
from the ring closure of the citral analogs. All the ring closures
Card 2/3

Ring Closure of Analogs of Pseudoionone and 3/079/60/030/05/15/074
Citral B005/ 'm 126
carried out are fully described in the experimental part. There are V
3 tables and 16 references, 4 Soviet, 6 English, 1 German, 4 Swiss, and
1 Czechoslovakian.
ASSOCIATION: Moskovskiy institut tonkoy khimicheskoy tekhnologii
(Moscow Institute for Fine Chemical Technology)
SUBMITTEDt May 21, 1959
Card 3/3

I.M., inzh.; GOl"UC-Rt I.A.t i,2z'j.;_ L111, V.D.s k nd.kliim.rauk
F~u mAhod of obtaining ctun-he;i:,6t.~ ~.nd a cariblmd ethod of
10 , -, '11', r.
obt4iining part -isoproXI- thylcinmmaldchyde
prm. ~7 no. 203-35 161. C 1.-11 1412)
1. Zavod "SI.ozhnyye efiry" (for Lob)(levt Gorker). -1. ::oakovokiy
inctu.itut tonkoy khiniches;;oy cj'-`lnoloCii imeni ..V. Lomonosova
(for Ilocimlin).
(Benzztld,clrr(.,e) (Cim-.Lmaldehyde)

MOCHALIN, V-.ao$ IVAKOVAp N.G.
SYnths8lS of acetals of TWI&aetylmde *MehyOs4 Zhw,ob,
kh~me 31 no.12i3896-.3699 D t6lo (KERA 15s2)
L Maskovskiy inatitut tonkoy khimicheskoy tekhnologil Imani
M.Lomanosova.
(Acetals)

MOCHALIN, V.B.; IVAINOVA, N.G.
New reaction of acetals of aromatic and heterocyclic aldet-,ydes.
Zhur.ob.khim. 32 no,5:1493-1494 Vq 162. (MIRA 15:5)
1. Moskovskiy institut tonkoy khimicheskoy tekhnologii imeni
M.V.Lomonosova.
(Acetaldshyda) (Heterocyclic compounds)

SOGDANOTICH, H.M.; MOCHALIN, V.S.- WIN, P.A.; UKHOV,K.S., redaictor;
PZTIRSON, redaktor
(Zlements of the theory of navigational gyroscopic instrunental
A;lemeaty teorii navigatsionnykh girookopichaskikh priborov.
Leningrad, Izd-vo OMorskoi transport.0 1956. 270 p. (KLRA 9:6)
(ayroscopa)

MOCHALIN, V. S. (Candidate of Technical Sciences)
"On the Question of Constructing Differential Equations of Motion of Certain
Gyroscopic Systems"
paper presented at the Second Scientific and Technical Intervuz Conference an
Problems of Contemporary Gyroscopy, Ye. F. Otvagin, Secretary of the Organization
Co=dttee; Leningrad, Izvestiya UchebrWkh Zavedenity, Priborostrayerdye, No. 5,
Sep/Clct 1958, pp 161-163
The Second Intervuz Conference on Problems of Contemporary Gyroscapy
Technique, convoked by decision of the Ministry of Education USSR, took
place in the Leningrad Institute of Precision Mechanics and Optics from
24 to 27 November 1958.

8/123/61/000/011/025/034
25539 AOO4/A1O1
AUTHOR: Moahalin, V. 3,
TITLE: On the problem of gyroscopic letitude indicators
PERIODICAL: Referativnyy zhurnal, Mashinostroyeniye, no. 11, 1961, 22, abstract
11D148 (V sb. "I-ya Mezhvuz. nauohno-tekhn. konferent-slya po probl.
sovrem. giroskopii". Leningrad, 1960, 157-178)
TEXTI The author investigates some variants of gyroscopic latitude indica-
tors and gyroscopic latitude compasses. 1) Double-rotor gyroscopic latitude
indicator with four degrees n? freedom and with pendulum, mounted on a platform
which is stabilized in the horiton and oriented in the meridian. Owing to the fact
that the present technology aces not provide a sufficient accuracy of orientation
In the meridian, It Is necessary to make the kinetic moments of the gyroscopes
Identical. and place them at an angle of 1800. 2) Single-rotor gyroscopic lati-
tude indicator with one spring which Is subjected to disturbances owing to in-
accurate orientation In the meridian. To exclude them it is necessary to use a
..,~,heme with two rotors and two springs. 3) Gyroscopic latitude compaas with
four degrees of freedom. The author presents an analysis of such a system, which
Card 112

.05539 S/123/61/000/011/025/034
On the problem of gyroscopic latitude Indicators A004/A101
shows that systems with four degrees of freedom, consisting of a gyroscope and a
physical pendulum tend to settle In the plane of the geographic meridian at a
latitude angle of the device location point. An approximate rating of the system
shows that in the case of a disturbed state the gyroscopic latitude compass cannol
be used as latitude indicator but as gyroscopic compass only. 4) Single-rotor
gyroscopic latitude compass with ring-shaped damper producing a restoring moment
around the pivot journals of the horizontal cardan ring. 5) Gyroscopic latitude
compass with sliding spherical pendulum, partly filled with a liquid in order to
obtain the pendulum effect in the case of a lag in the displacement of the liquid
relative to the chamber, this effect being proportional to the angular velocities.
The given system can have some prospects only in the case of considerable values
of the kinetic moment H. 6) Double-rotor gyroscopic latitude compass with
spring, representing a combination of a gyroscopic pendulum with three degrees
of freedom and a three-degrea gyroscopic latitude Indicator with spring. 7)
Double-rotor gyroscopic latitude compass with two pendulums which Is also a
combined system of gyroscopic pendulum with three degrees of freedom and a gyro-
scop1c latitude indicator. There are 12 figures.
N. Rogov
[Abstracter's notei Complete translationi
Card 2/2

MOCH (Docent, Candidate of Technical Sciences)
"Theory of aperiodio gyro pendula"
report presented at the Scientific-technical Conference on Modern Gyroscope
Technology Ministry of Higher and Secondary Special Education RSFSRO held at
the Leningrad Thatitute of Precision Mechanics and Optics, 20-24 November 1962
(Izv. vysshikh uchebnykh zavedeniy. Priborostroyeatya, v. 6, no. 2, 1963

MOCIIALT'll, V. V.
Fisher- Products - Pr~pservation
- ~ 1, ,
- -b. k "' 'c'
, rorc;7, he p.-opooal c-f cnf- nef--,-r G. A. Kirichenko, Ill hnz. , 1,,' 1, -II
9. Monthl List of Russian Accessions, Library of Congress, July IA? Uncl.

MOCHALIN, V. V.
Fishery Products- Preservation
E~cperience in using polyvLnyl chloride linings, Pvb, khoz. 21 n . 7p 1952.
Monthly List of Russian Accessions. Library of Congress. November 191).1. UNCLASSII,'IE-,)

140011ALIIA, A. S. Cand Biol ~;cl -- (diss) "The hemolytl,~ of tirsuies
ULIJ)IN
,rliirin;-- the nction of ionizing irradiationj 46i the orgrinism. " -*-Ios , 16 lDp
(Acnd Ifed Sci US6R), ~50 copies (KL, 13-h8, 95)
-34-

USSR/Human and Animl FbysioloCy. Dlciod- Formed Elemnts
of Dlood -
;,bs Jour: Ref Zhur-Diol., No 12, 1.958, 55430.
Author Mochalina, .'.. S.
Inst
Ti.tlo The Toxic and Hemolytic Factors in Inimal Orgrrmioms
at Irrad-iation.
Orig Pub: Tr. Vses. konferentaii po ned. radiol.-Eksperir-~-
md. radicl. M., ~k-dgiz, 1957, 68-72,
,'.bstract: Mice were diseased by Co6o (with a fatal outcot~--
on the 5th to 6th day). From the oreans of the
Llice killed at the onset of the disease, water-
saline extracts (E) wc-re prepared. Due tc the
irradiation, such E have acquired heiaolytic prc-
Card 1/3

TISSR/Ijumn and Jtniral Physiology, 131ord. Fomed Elements
of 13locd - T-4
Abs Jour: Rf Zhur-Diol., No 12, 1958, 55430.
perties and destroyed the erythrocytes of the rAce
in vitro. Thus, hemolytic substances were first cf
all discovered in the liver (one hour after irradia-
tion in 50 percent of the animals), and also in the
spleen, where the largest number of them was fcund
The hemoly-tic activity (HA) was mrked most and ap-
peared faster in 1:20 solution samples; it was
weaker in 1:10 solutions, and quite weak in 1:5
solutions. W, was not found In the renaininC San-
ples. The Hit cf the liver and spleen in E increased
after irradiation durti~.g the period of 18-20 hours
following the irradiation. This increase was espe-
cially i.iarked 42-48 hours after irradiation. Only
after 48 hours could the W, of the brain and of the
Card 2/3
50
USSRAW-Min and Anir.,al Physiulr,LV. Dlcod, Forred Elenents
Of Blood
.b3 Jour: Pef Zhur-Dici., No 12, 1958, 55430.
kidneys be noted in E The water-saline liver
extract of irradiated Mice proved to have specific
properties, and did not effect the erythrocytes of
rabbits, guifise Pies and hurjans.
T-4
Card 3/3

-2 :)26C'3/:)3G2
c?il-.1- in-- . A. and K1-- a-m-ay i e
T I T h e r. flf'e c t ~j fcr c t e c -It; i v esi n c e C 0: sor:-)-
tion, cli,;racter.".stics of
-auIiobio--'oC-iya, v. 2, no. 1, 1962, 1121
T-E'XT The dyn&ziics of c.'Ii--n.L:,e under -2.e influence of
colloidal ,.c 110 in sc.:-15tion ch:.rac -,e r-i s tics st~~diel~ -i-
~-ssue of 3 f-rouos of wh~i-,c mictD (vieJ-1-t 21 - 25
ted; 2) exnose~ o C060 Ca;:--!sa-r,-di~~tion at 650 r; an,~ 3)
j 1 1 14 Lne
at 3 and 16 min. after ra-;io,~rot,3cIjve '~,eta-mercaptoe P7-
c 'steine Given ,"'G C-3--
ly at ~ a- d 10 mous e
CIL'! solution at 0 . 2 ii . vi iEM a. c t i v o 2 c s i v e n i nr.- -
Venously, and th-e mice ~ciiic~d 2 i'.ours !-,ter. 3orption c--. ra c t f2 rP, -
-.ics in tissue fro-..-i 1-~ver, spleen, kidneys, small int,1
and of blood viere deter:7.ined by t -%e extent of ra-io-active At
.L . he intravenous introduction o-~'
accum,u'ation. Exoeriments wit", t"
A6110 showed thai the main body of cDlloids 6is-,ppeared fr~-,m the
Card 1/4

S
S110051621 C 2 // 0 r" '2'
The effect of radio protec -, _"ie
blood in first ;~ ',ou~,- aftur inocu_~,+'on _I~ie ~-j
tion by ori,ans and of tl.,
the ori-ans and tisoue of healthy mice s~~C%.!e-.L'
irk liver, and tiaen in "kirneys , sp-I een, in-.estine, an-., ,,n;s.-le
in descendinC order. 2 hours af-Ijr irra:,irltion was -:- 7
nt,y 3 F,, TI-I iv or
increase in sorption in iiver, sTlaen, and
it rose to a maxlmum of 56 , owr nor~.,.al --,+. 2 4E~yp ~In`
at 24 hours to )2 ""', declininr- su.oseauently, but :'emaini-n;- ur, j
normal. in mice given be'.a-:'.ercaptcethyiaaine foilo%-,re~
n spleen an] :~.Lneys increace,_~ by --n4 C r' r
17
tion, sorption 1 4,
spectivel-i at 2 hours. in liver --.t 24 ',-ours t ere. _~s a
crease, ther, returr_~n`- to ncra.al. !.'n spleen at z t,.
was an increase. There %va;3 P. -rao'ual decline In
hours Agilo.a2CUIMUlattiOn i.-I LI-le intestix:e
subsequent clecline. ;"'esu-7ts si~c,aed that the
nercanLoezhyla:~,ine and o: cysteine Oefore
the sorption charactcrio,,ics of laver -tiss_e.
to nealthy mice intraveno-sly ::as unequaLl.;
-ans, with nighest acc"ulat4Lor iri liver, an'-I lesS in
Uard 2/1+

"12(
) 5/ ~-; 22
The ef-fect of radioprotective ~26E/3302
are 1 fic;ure and 14 refere!~ces: 5 bovie-u-blo c LLA- -!A en-
The 4 r.~,ost recent refere.".CeS W Iie
read as follows; A. BoSc, internat. J. 'tad.
hambach, J..,.D. Coo-)er, H.L. !-.It, H.IT. %ro~--el, j.',','. Clar!~,
D.L. Jordan, --tadii.tion :Ies., 10, 2, 148, 11959; D.D. U~-,~r, i,.2.
Parkins and J-G. verei-kes, Hadlaiion Res., 11, 6, A.
Uanz and 1-:. Brucer, J. Lab. rl"Iin. j"ed., 52, 1, 2L, 1958.
SU31-,ITr-'E'D: July 12, 1961
Card 4/4

6 2,1 C 21 2/
fhe effect o f raadio,)ro-~uc :) 2 6 8 X'JO 2
ne-,,s, intestines arv` ot~~,tr t'_'_--,ue- '11.e
t_ese tis~;ues ircroase~ 1.1'. %..Lce ox~)Osei to
--'cs-, bu-~ differez'
,.,-ents st"I",
1 4C S 2
or,, r a c r I s __I C C,_ C
c., ar-es in s on C',
c aL cr.emicu' a' -,e_- tio-n t,-ie bi3s'ructuros.
ced sorption of rad-_;,3co_1:)i~LL1 in !,_ver t 1 7: e ~r_ -
r c an t o e thyl am i n e w a s e n b e f 3 r e i rr ad i -, t io n i.-. 2 1' n e r
Versibility of tie o c a s:-~ . 2'-is di.! not occur ---n s'p-Leen
d,,~e to t',,e deep dest-uc-i'le C-~!-.i-es. Cystein 5 min. "-fofe
, -110n
rec'uced accu!nU_;_U_ 0- .0
C060 at 0.1 i.-,c/6 peritorea'!,r
in liver, D_=creas, soleen, an,~ otl--er tissues in c a
i2 attributed to the spec4_fic effect of s t 0,-v a c:,.
cell penetrability. In conclusion the introductic.-i of ~c c
substances has a normalizinE; ef_"ect on the sorntion
of liver wl-,ich in turn affec"T. t,-e roversibility of .he
processes in the irradiated orCanism and redices radiation sJ_1c1-.ne3_;.
T.'-,ese substances also increase the sepa.-ation of ra,!ic!~-.ctive
oid through the liver, li~e,,,iise reducing radiation sicl.:ness.
Card 3/4

IWAMAYDE, L.L.; 1,I)CHALMAI-A.'S'.
Ac tIaA ~of , p=jpIw, -1.11 substances in internal and external ir-
radW4~4 e- _==.'Tfddy' MOIP. Otd. biol. 7:127-131 163.
(14IRA 16:11)
11 f

TERLNTOYEV9 A.P.; RUKRADZEq YO.G.; MOCRALINA?_j*G.+-RODE, V.V.
Synthesis of 2p6-diacetylpyridine, Zhur.VKHO 6 no.1:116-117
161. (MIRA 14:3)
lo Mskovskiy goaudarstvennyy universitet im. m.v.Lomonosova.
(Pyridine)

25320 S/020J61/138/005/020/025
9'. 909 0 B103/B220
AUTHORS: Terentlyev, A. P., Corresponding Member AS USSR,
Mochalina, I. G., and Rukhadze, Ye. G.
TITLE: Polycondensation at the interface
PERIODICAL: Akademiya nauk SSSR. Doklady, v. 138, no. 5, 1961, 1130-1131
TEXT: The paper deals with the synthesis of polyamide from pyridine-
2,6-dicarboxy'lic acid dichloride and hexamethylene diamine. The.authore
applied the method of interfacial polycondensation, and stuJied the
properties of the polyamide. The above-mentioned method was suggested by
E. L. Wittbecker and P. W. Morgan (Ref. 1: J. Polym. Sci. ~LQ, No.-137,
289 (1959)), and is superior to the existing method of polycondensation in..
the melt. The most important factors influencing the y1eld, moleodla'r
weight, and viscosity are the nature of the organic solvents and
emulsifiers used, the concentration of the reagents, and the stirring of
the reaction mixture (R. G. Beaman et al., Ref. 6; J. Polym. Sci.Rot
137, 300 (1959)). The lutin-containing P-picoline fraction (residue
obtained in the production of the preparation ftivazid (A. P. Tereatlyev
Card V4

Polycondensation at the inter&aic-e"
S/020/61/138/005/020/025
B103/B220
et al. Zhurn. Vaesoyzn. khim. obahch. im. D. I. Mendeleyeva, A, No. i,.li6
(1961)) was used as initial substance for synthesis. The synthesis was 4V
pei~formed by stirring in a chemical test tube at room temperature
clzc_(~COC3 + NHI(CHANH, -tcq-c __-N
No*
CHSCOO o
Not
Co.
N&O"
The above-mentioned acid dichloride wds obtained by boiling the acid
mentioned with thionyl chloride,and then dissolved in benzene. Freshly
distilled hexamethylene diamine-Ras dissolved in aqudous solutions of
sodium acetate, sodium carbonate, or NaOH. The pH-valuee at which the.
polyamide was precipitated, were measured with an 4111-5 (LP-5) tube
potentiometer and amounted to 3, 7-8, and 10, respectively. If the two
solutions were simply poured together, a polymer film formed on the inter-
face, which could be extracted as a fiber with a a mall glass rod. A
polymer precipitate forms in the entire solution while stirring. After
filtration and washing with rater it was seliarated as a white powder
soluble in pyridine, concentrated formic, hydrochloric, acetic, and
Card 2/4

2532-3
Polycondensation at the interface
S/02o/6 1/7 38/005,'020/025
B 103/B220
sulfuric acids as well as in dimethyl formamide and when heated in
m-cresol . The polya-midp could be pur,.fied only by reprecipitation 7,1th
ether from pyri(iir,e z3_j1ut,,or, Its .n'ringir v1s(:csi,y wau measured in
concentrated H SO -and in dimeiny" formam:dn '-.I -Le U~,belhcj-
2 14
visr-c-simeter ;it 20"C' -ino .vq3 e lua or ,i H- va lue F,
mentioned. lt arnc-.in-,j C ~2~ n HSO,, -s 1 -1 iT,
of 0,5 g,'100 [1!, 1!:
M, S 'x, 1:~
0 r ~~C f,
%1;1!1 0,5.,, C-.i 'C r r i i
C, C) 0 0 T h
thermnmpr!lian ira', our- ipe~i-irr?d t~y Kai-gt n ~3 balu,,,, e ibatrac t,~,r' s
note: balance riot stated] . The infrared spec tram s!;ovied', th.? exi sting
N -H and C -0 bonds. Th F, N - 11 f'r P qu e r,- y is 3 3 52 - 3 5 7 8 -- Ln an d t h e C - 0
frequency 1652 ,-m-1 3 1 r, c e c r, a 1 rn N n c t io na I gr ~~,j ~, - (~ h m 1 Wh t E i v e
c h el a t P n od e 3 h ~i t h a 1 ~1 , w,i vi ed -2!) r. rr,,- t:i 1 1 t 3
Card 3/4

Po lyco r-d c, o
Polyccndor.-,~itio,~ 7~f
ro 7t n r r -
ind r;.
r e fe r e nr e Er~
e fi t T* C4.
So 1 4 0 1 J7, 2?q Q/)
SUBMTTTED:
0 2
rA
f F- d~iri:
r
--i n S K r P') I YTIJ
Card 4/4

TMMIYEV, A.P.; FEIRM, Ye.G.; VCZZHENDIKOV, V.H.; TAYON OVA, Z.V.;
OBOLADZE, f#.S.; KOCKALINA, I.G.
Concluotancl and activation energy of chelate compounda of
dithiocarba~tates and thicamides,, deriratives of pyridine.
Dokle AN SWR 147 no.5%1094-1097 D t62. (MIRA 16:2)
1. Pialko-khinicheakiy institut im.
gosudaretvennyy universitet im. H.V.
pondent MY SSSR (for Terentlyev).
(Chelates) (Carbamic acid)
L.,Ya. larpova i Kaskovskiy
Umonosova. 2. Mlen-korres-
(Amides)

ACCESSION HR: AT4031995 S/0000/63/000/000/0123/0128
AUTHOR: Terentlyev, A. P.; Rukhadze, Ye. G.~, Viochalina, 1. Go; Panay&, G. V.
TITLE; A study of the chelate polymer series. IX. Polymers of some thloamides
and polythicamides wi,th metals
SOURCE: Geterotsepny*ya vy*sokamolekulyarny*ye soyedinentya (Haterachain macro-
:molecular compounds); sbornik statey. Moscow, lzd-vo "Nauka," 1963, 123-128
TOPIC TAGS: chelate compound. polymer. chelate polymer, thloamide. polythloamide.
chelate structural property, polymer structure, che.late trans configuration,
chelate cis configuration, polymerization
ABSTRACT; A large number of chelate polymers were synthesized by equlmolecular
reactions between thioamides or polythioamides of alpha-picoline or 2.6-lutidine
in a suitable solvent (dimethyiformamide, chloroform, benzene) and methanol solu-
tions of metallic salts (Cu, NI, Zn, Co. ha). Yields ranged from 39 to 93%. Cal-
culated H content from 9.00 to 11.60%, deiermined N content from 8.12 to 1l,.89%,
respective metal contents from 10.33 to 15-93 and 9.96 to 15.85%. The polymers ob-
tained were yellow, green, cinnamon or orange, or in light. dark and reddish
shades of these colors. Three types-of chelate structures are Illustrated. the
ance of tetra- and pentacyclic linkages Is suggested, and the authors discuss
e.27 , / 2