SCIENTIFIC ABSTRACT MAZOKHINA, N.N. - MAZOROV, YA.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001033130005-5
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: June 14, 2000
• Sequence Number: 5
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

MAZOKHIM,_,X.N.-; BOGDANOVA, N.V.
Capillary method for determining the heat reolstanoe of
micro-organiams, Kons. i ov. prom. IS no.1202-34 D 163.
(MIRA 17:1)
1. MentrallrWy nauchno-issledovatellskiy institut konservnoy
i ovooheheaushillnoy pronyablennosti.

NIKOIAYEVA, S.A.; MAZOKHINA, N.N.
Development of toxigenic strains of a Clontridium perfringenB
culture in canned food. Vop. pit. 23 no.5t7l-74 S-0 164.
(MIRA 18:5)
1. Vsesoyuznyy nauchno-issledovatellskiy institut konservnoy i
ovoshchesushillnoy promyshlennosti, Moskva.

KAZOKHIWA, N.N.
New State standard "Canned food products. Methods of bacteriologic-
al ana3,vsis.0 Kons. i ov.prom. 19 no.1:35-36 Ja 164. (KRA 17:2)
1. TSentrallnyy nauchno-isaledovatellskiy Institut konservnoy i ovo-
shchesushi2snoy pronWehlennostis

APT, F.S.; NAZOKHINA, N.N.; NAYDENOVAI, L.P.; ROGACHEV, V-1.
Microflora of products irradiated by gamma rays. Hikro-
biologiia 33 no.1:167-171 Ja-F 164. (MBA 17-9)
1. TSentrallnyy nauchno-issledovateltakiy inatitut konsermoy i
ovoshchesushillnoy promyshlennosti, Moskva.

MAZOKHINA-PORSHNYAKCYVA, N. N.
"Soil Saprophyte Bacteria as the Cause of Vascular Bacteriosis in Kok-
Sagbyz.11 Moscow Order of Lenin State U imeni M. V. Lomonosov, Moscow,
1955. (Dissertation for the Degree of Candidate of Biological Sciences)
SO: 14-972, 20 Feb 56

'I I

", z,7 . " ~
~ -.18,
MAZON, )kris; BOHDANOWICZ-CIESKI, Wanda; BERWIN-KRAJFWSKA, PArts,
Determination of iodine in certain contrast substances.
Farmacja Pol 18 no.13014-317 10 Jl 162.
1. Instytut, Farmaceutyczny, Warszawa. Dyrektor do spraw
naukowych: dr. Pawel Nantka-Namirski i Zaklad Analityczny,
Warszawa. Kiei~ownik Zakladus mgr. Wanda Dmowska.

0 0 00 0 0 0 0
)%2fnFIj
a Poocissis 440--* .-P, .1 fl
4k
00
00
*0
00
if mm )431 ).Rapti 61 Qu ".DEW
A-A-A-t-L'A
PrismV34 Chm. 17, 41-CM).-OAGN In the W hutkm cd
by owmag few slowl with sub7d. Ir i, add. evem, wow
-Islysm Imming elters. HON in wmu wamthin *et& up tbis
m0 Luw causes a dwa CARM Repelled of matb Ame*
matx. =r.;:tl of HIM "Sulu to a m nK-dw witbond ptiyn*ra&. =00
tke of c&fim. The prodws we kimstea of and totWy Am and besyl
&Us. Cydins n:sWts m simca complete tmvmW cd loonk Wd Itto the estm.
A. C. 2whfim Zoo
SLA ImIlAtILIVOMICAL U111111,716,1111 CkAMICATIO
flow t1w"611.4
U It At AD
I
Soo
Vi 0 of 0 0 0 0 0 0 0 4 a 0 0 0 a
0 0 0 0 0 0 0 0 IS 4 Yff
900 Sam,
40
zoo
'00
t's 0
A3 s
I, At
440
0 0 0 0 0 0 0 0 0 0 0 0 a 0 a a 0 0
19 a 0
6 0 000 0*6410 0 0;

;*-wow* *i' g
a a v JILM v at a x v a 0 a #1 62 0 0 4110 a
a 0 0
At- I AIA -a
psvcfns~ AND roupf"'Is "I a
J1
Sea
so a
*ddim #A rmvdiiiiiiiiiio to smW tgb&,L lit,
NWWMM. Amasim Ewa. 146.136v
N. A~ A. zoo
see
Sea
Igo. see
cog*
wee
coo
a**
IN
zoo
IN
, 10 wee
#--I! a
N
10-
too
V . 44.AHM
W~ RX,
on 0,0 0 go Wo 0 O'S 00 00 to 00100 00 00 00 :41 :00 0 0 0 0 0 9~

0 44 0 O-A a 0 0 0 0 0
0000000 0*00*0~04vftoo 0 ~400000000000090oie
v It u 0 w b h u 0 2 --ram-sox A?JD j*A jo v *Joe if All] ad &),to
'A I k~ I & - - 0 S-1- -
W. 0-0 too
000 00
of bummumpolhak Dew T. mamw -00
OOA
Pnmyg Chow. 15.
b0.., swbw&
na wAkmika mW. is =bjcntd to a Pnxvm of cOn-
*0 duams ma. VIM C04 in Id Im " 11111-1 / C) 4p 0
C*W Wumn matent ia
wbn the ewdre F%BWI -00
j, the CJ36 est., 1mv * mifte of 81.8%
%~n. wbkb shtf 66&.--j# amo wyvw ftw the oullons- ~00
rt of the C*1% uwd aml"w% -00
0 tkm of tbr wal baicb. ft
:,,!t
R. C. A.
-00
0
"o
00
00,41 00
o9sl 00
0 -00
Eli j8eei: 'goo
zoo
-00
1p. WERAtUOR 0 0
ka;j-63 .1-0 C', Ofti ltillwt' It'll, ~11 ~00
u .0 AM A a 60 0 10-01 1 v 14 .1 ADI
ft it AW a R IF a 4f a Kill 41 INA
n0OW Soo 0 90009009000,0000*0000006006060
0000fooooooooooooo~eeoeooioooooooooooooooooo

off *** 414141 111
0 01 Off 1
0 44 #1 W al 9. 0! 46 m44 V,
00 :06

-60

1bv Owil" Optlitnob of dam- abd bydrosy inall
,
h
b
I F 1=
0
~
l
l -00
00 i
11
a
tro
easomil.
4
04
t
, . -
1140-90-
16
A-377" -00
00
sea .
.
milvelsing )%NO~ (1). Colls(OlUs (U) and fumins 1ICI
J~jjjj yLAIrd a mixt. t4insiming of fi-chillro- (M). K.
-00

0 a

liou-
r
rI
1,
l W te,0
al
IvIl
h th
1
l
t

0
11
.
lwr%
g Mail* vm1
lum
1
t
lw
W oblointd. 311 0. -00
T
IR anil 1:0) If. III writ tivatrill In 2 mi&d mlilem Im
8 hro. ski IM-70'. Thr travilln) "At. aft" vivoill 4114111.

00 4? 41111 fill ratilm WIA dim 4. roe
2 8 A. 44 MV& V1 while OW ellem oil Wall Ilddnl to III%-
04 3 mly ImPthict Used in wmkinx 4p TV. Thr fri'lil1w In tilt
:
li-m. Rank after hmi,alisalkos with alkali was rxid.
withEW.

00 3 yieuled a clear auln. and a tarry rAm Irm which V111 was
00 W obtained; 432 S. of the restiltant. cmde, c1m, M204ree :7
roe
oil disid. im; varbo (4 =1n.) at W-140" pvc 4,2 g. 4 %Aid ,
900
so it
and 39 it. of ody distillair to which was addrd 44 g. tJ
cir
of IV
m
In
nd
34% IINO
Th
it
t
ft
1.
z
*0 . a
r n
ra
e
a
er se;
~.
.,
"
i1 whi
t
it with N
OH
21
5
f
h
lidifi
d &ZOO
o in"
Itta
&
.
o
c
go
r
gavt
S. o ::Zoo
f 9 in tolp and in. 41 C. T. Ichniowski
goo
goo
WOO

SLA INOULtURG ICAL LITINAILOE C1.01411FICAVICIP too
*00
xpgw 11pgal.0
S02044 VIP av oaf 1,

-
-
-
-
in-
0
40
I w
14 two a .1
3
Ir wtija
7
W
a, .0, a Name Run IIIIKWO I;m 2 0 W -
0 0 0 *if * a a 0 0 a f 0' 0 & 0 0 0 0
0 0 Oft 0 0 0 0 0 0 0 0 0 0 0 0 0 0 a
0 0 & 0i0.0 0 0 0 0 @*'1* 0 0 0 e 0 0 0 0 efoooevoo 0 0 fee
:1 0 0 0 0

1 "Toro
mil"U
lit . set

12w feartlitts of 0. "d P-skirown"t oat 0-alftepat"cd
ads. ~~T_ maz0hall,
*
1
Mi
I
d
r
al
R.
Ax da. Rmviki C".111,
*11it-W
00

aft-
b
"
h -00
0418 rc
owe
m
eated *Ith 11yeacd MW IT in kht
tinled tubes to IM-370'. Prom 0-ultrotolacne them *a,

dilrotolocur 2 cwppds. wen obWard: 6-methyl4k. .00
c-MwoquioWir,r, m. Q.Al, antl Front MOO
eve
Of
) o-nituipbenol. SwhkwcpS-hydroxyqujaWjjw, tit, 1240. and
9-hydioxyquinigint were oblsM in almoovi rqual
uan- =00
6 q
141 wpicirchowski zoo

'00
00

sea 00
00 z
00 9i 00
see

S L 4 OffACLUX'GICAt L#TCRATU*l CLASPPICATICO
J... WOO
----------
r

. . ii
u 1'
, oil
v r I
us oil m
' & St 0 0 0 a a 0 *1* 0 0 0 ***sees see *st
0000000 so*** go

IN 11"h1lbol AS.
Todr
23. 3111-3N 194OX Ba, lish bm-
wilt N-0100
drorribed in Ger. M.M. C.A. 31). WHOD) wasivinvesilimed.
the rr."im produrb we 3 ioamrsiv vulto sinim) diphLayl
su%drs (1) 0' 2 4' wid 4.4'). 1M61. of thr ;wmv4lwc
which giv%W& jiS6;t yields (75%) of thew 3 products sue
described. The 3 wilw t P'kwyl SMIA&j. purifird by
repestedcrysto xu.FA*,lG5.5'.andl4.3*,mp. Thtywric
reduced tollit imbich weft converted
to the N,N'~H-Ac derivs.. and the Utter purifird awl tv-
AMM-led tothefree minintsin veryputeluctn; di-Acdcriv-.
M. 1644% 2M'. amd 216.5'. resp.; the pmAW free munimes
ru.#ro*.6I*.%ndlO8-I09'. Telrazoli" anti coupled with
Naplitboll AS, the 3 dWakits gave dyes with very di-Ahict
fifferearts in calot. The ortho-artho deriv. gave a scarlet
(brillit red) sluide, the para-puir deriv. an armArmuth (ied.
violet) Aade; tire ortho-pwa txLbe dyes the fabric an inter.
tnedhite shimle. idtatical with that given by an at
m6t. of the 2,21- and 4.V-Ixvws. In the course in-
vc3fliatiOns dmoibed were also prepti- "ydroxy-2'-milradi-
Pkrxyl ssdfi&. in. 162". and its di-Me cilict, in. A-9.P. 13
MerrixVs. FAward A. Ackrrminn

MAZO-INSKI, T.
MAZONSK10 T. Ten years of the Chenical Department of the Silesian Polytechnic
P. 329.
List of papers published or submitted for publication by scientific workers
of the Chemical Department of the Silesian Polytechnic. P. 334.
CMMA. Katowice., Poland. Vcl. 8, No. 12, Dec. 1955
SOURCE: East European Accessions List (EFAL) LC Vol. 5., No. 6, June 1956

PaLAM/Orgwdc Chemistry - Synthetic Orgwdc Chemistry. G.
Non, Jour Ber. Miur, Rhimiya, ND 161 1958$ 53776
Auth or Hazonsky~ Gosbc,hinsky
Title Sulfur Derimilves of Steaile-Acida
Orig Pab ZeZh - nauk. 1031te~- slaskieJ, 1957,~ Igo 12, 27-34
Abstract (ri-C1.0 CHCbDC9)2P, (1) vas synthesized. Thirty eigat
Zrams, ne warvedded over-a period of 45 minutes
op=
'with contihu~us stirring an& hedtli2gAo a melted mixtu-
re of 25, grams~'-of -stearic- adld'6nd: I gram of red pbos-
pboruse ~ Ifte.-jr 4 to 5 h6urs t^-~1000CO, the mixture
vate'r andl.3-C'O CHBrCOM (U) vas ob.
33
=ZV7
A niktui6'of 11 and MIS in alcohol-As boiled for two
hours in'an~attobvphere of nitrogen,,-emd
Card 1/2

lyNZO-Nsk

432
otom
On.
way). 80
b
no mj lpos., Slo y. ft
w 0.
llow
pivlim. 4 11) 1~ it, j P&AMORi or t ow IOU -
(1) U;

?or
OR

d'"d Rf3OH wis the simm
ol to
i
od
h one
knd*tr l
m
,
.
t
we
c

X-1
-
-
A from
~7~05 OW a it Oktks for,~- Ob bd"vaj

in
Ofsp are.
'd
SAM. -'4nt4i),Cx
Ir6dIo
I
I
-
os
oldfa
j*od iyreh~: i *Mle% FT
cz,
lemYs Cheml
a C-

conornical, ut)
ibli U,40r!
Paw. ith the MW - uZatim;
' qc ;5CL
)f 7fQr

48 1 J41j" 8104
Al r
fo
,
'

- I ~-I
v~t~ *
-ma &d%Vjfig'jI In' SAM
~Wyreil* Wd at
to
-

at -the
-0 one D W u skyarl,
A,
of the Iii0s of vtbry.~ exaninatIon- 9U the ethylem-pnolenk,
labor
COW, KNR-MeA,

% to WW ve c6nu~t:
A*#"l felt""
I
.
u
s tanpers
ROM1.4 to 113 AW; e, optimm 1kne amtjid% vA vario
,
,
e`*- jp` a e*UkbU*
e$ aw In dl p CS ~,Wl -topther with he bed
'
Y 4. of." ethylene mW "yleiw t
-,Iiwh c6ndl Writ
7**#4 %incia
Vitt
-
,
on the
prme" pg nvmvwan",~ St y .1ho
'at 150,C. W
me. -WA vapour on 0' ire
that
a ~2,5 sm) stimed the
OWMft ClDapnt Ed water. in. the mixtu vm~~ Mi b~ weisM.1he:
re
1
Cj~
L
PrWY ne 4n4 XW4 WSW: rewectIVOY: 3704,

7
77

5~ v

a

5W,
HIM

-Q- JWa)Xy'cznnh Ocanicznjvh pokezeb Amplekmw

"
lose A
No
9
II
chemlemy
P"92
b
.
nu
.
.-
.
.),
S
-
,
"
'
latimi cd be wt sor
th
in
Vesuiotknis amerned of
es
".7jyt ohlaride in 4tio. V; resence of- i'imninimn ebl6rkle ~ aDd 114,
m ~. settvatOd with 'hydrolcii.- chlcildj ar - xniiury,', iho-7 lost
'
l
h~
d
i

" a Catalyst 10
t
lakly ellident
a
ky'4uw
prmed
11ouvver
the ylOds
gamyl chlaW
j
,
.
l
thm Wa w a
lia'otnrl.
CH
-OM*eX MMDMdS. Ooduc~a d~rft the, Teia cc . en
cWorlde ma cl~ benzene In the'prawnce al- artivaW sit imk&vn, wwre
fle3imt.cautysts of- a*34ollom The coxv tx
mom er

ted by i4ildmi Ai ii~t
bat Ock vatab"lic vTo~eitlwcian
RmAlvattA maplex
-adoed 34TY stable catalysta mA may -bB used many met.

ti

m
M
T ow

SU

OW
A I
on
Mum
-
lbo. ot 61 AlClevi xdtW
'
itd
Al -
w0 to
'
K.the yleld *6
ibj4..- -AIMi vat as
-
0-1/2,0001t;
I
-UCI
Al mict~w 'nilb
WM U"d.Wtrp ip hesc cow

4nd-*hm'
0 tattlyA vvtt~ "d ova, lllta~. . th
th "o
~rd6wgioreftP4, eywts vated
vij.M

P/014/60/039/003/004/005
A221/A126
AUTHORS: Mazofiski, Tadeusz, Taniewski, Marian
T=: Investigations on pyrolytic decomposition of propane-butane mixtures
PERIODICAL: Przemys-1 ChemIcany, V. 39, no. 3, 1960, 170 - 175
TEM This article is a continuation of research described in Prz. Ch. v,
37, 175. Its %Wj%ct was pyrolytic decomposition(of synthetic "gazol", i.e., the
mixture of liquefied propane and butane. In subject %rtiole, pyrolytio decomposi-
tion of natural "gazol" (natural liquefied gas) is described. Ths.pyrolysis was
carried out in heat resisting steel, stainless steel "KNR" (18/8), copper and
quartz pipes. As a result of the study into the influence of temperature in the
range of 650 - 8000C and c:)ntact time 0.6 - 127.5 see. on the courde of the pyro-
lysis of propane-butane mixtures to ethylene-propylene, several regularities were
obrerved. Optimum contact times have been found at various temperatures and in
reactors made from materials mentioned above. Confirmation is given of the pre-
viously deduc6d enpirical rule, which established thit the logarithm of optimum
contact time, in the range of temperatures examined, is a linear function of
temperature. In the reactors described, using natural and synthetic liquefied
Card 1/2

P/014/60/039/003/004/005
Investigations on pyrolytic decomposition of ... A22i/A126
petroleum gas, the weight ratios of ethylene and propylene at the given tempera-
ture and optirm, contact times (ethylene-propylene pyrolysis) have been found to
vary within fairly close limits. The composition of the "natural gazol" is:
H2 + CH 0* 3 0.1%; CO = 0.1%; C 2H = trace; C H - 0 *3%; c H. - 48.9 -
ra tional materMs have lltt~e effect on
- 46.R; GAO 56.2 51.4%. ConBt2
results. There are 9 figures, 4 tables and 6 references: 2 Soviet-mbloc and 4
non-Soviet-bloc. The reference to the English-language publication reads as
follows; (Ref. 6: R. H. Kinney, D. J. Crowley, Ind. Eng. Chem., 46, 258 (1954)).
ASSOCIATION: Katedra Technologii Chemioznej Organicznej Politeohniki Slpkiej
(Silesian Polytechnic, Department of Organic Chemical TechnoloRy),
Gliwice
SUBMITTEDs October 20, 1959
Card 2/2

- MAZONSKI, Tadeusz; GASZTYCH, Dyoni2y
Studies on the alkylation of benzene with low molecule olefins
I
in ~r presence of alwni~um chloride. Pt.l. Alkylation of benz6ne
with~propylene and butylene and dealkylation of dipropyl-and
160.
no.6t332-;.336
dlbu~tjlbenzene.
Ja
Przem cheift 39
1. Katedra Tachnologil Chepicznej Organicznej, Politachniks Slaska,
MiVice

Y.-SIS00
2741B
P/014/61/040/008/005/008
D233/D305
AUTHORS: -Mazo:hski, Tadeusz, and Hopfinger, Alfred
TITLE: Reactions of benzene with higher chloroalkanes in
presence of AlCl3
PERIODICAL: Przemysk chezaiczny, v. 40, no. 8, 1961, 453 - 456
TEXT: An investigation of the influence of various parameters on
the formation of alkyl benzenes with higher alkyl chlorides was
carried outp since little information about these systems has been
published. The alkylations were conducted in presence of anhydrous
AM with primary decyl, dodecyl and hexadecyl chlorides and with
mixtares from the chlorination of normal decane, dodecane, letra-
decane and cetane which contained only a small proportion of pri-
mary Shlorides. The reactions were first carried out over 2 Y2 hrs.
at 70 Cp using a constant 5:1 ratio of benzene to the alkyl chlori-
de and varying the amount of AM . Length of the aliphatic chain
and position of the Cl atom had n8 effect, apart from slightly re-
Card 1/5

2742
P/014/61/040/008/005/008
Reactions of benzene with ooo D233/D305
ducing the yield with increasing molecular weight of the chloral-
kanep although the secondary chlorides appeared to react more rea-
dily, The optimum molar ratio of AlCl3 to the alkyl chloride was
in general found to be 1:10. The reactions did not proceed to com-
pletion when AM 3 was low and the yields were decreased when the
catalyst was in excess. This is ascribed to 'the occurrence of side-
reactions which are described in some detail. It is believed that
in the presence of AIM 3 the chloroalkanes undergo dehydrogenation
and the H2 evolved reduces them to the hydrocarbons. Formation of
olefins, cyclic paraffins and free radicals is then postalated. Se-
condaryreactions consisting of alkylation of the benzene, polymeri-
zation, condensation and formation of complexes with AM 3 may
then take place. This mechanism is supported by (1) formation of
paraffins of the same chain length as the original chloride, when
AM 3 was in -excess (2) evidence of the ability of A1013to cataly-
Card 2/5

27W
P/014/61/040/008/005/008
Reaction of benzene with ... D233/D305
ze the reduction of chloralkanes, found in the literature, (3) the
formation of an oil of a high iodine number after the decomposi-
tion of AM 3 complexesq and (4) presence of hydrocarbons unsuscep-
tible to sulphonation in the products obtained. It was confirmed
that a preponderance of benzene in the starting materials favors
the formation of manoalkyl benzenes. The effect of time was stu-
died using a benzene: chloride : AlCl 3 ratio of 5:1:0.1, finding
that the optimum yields were obtained after 2 V2 - 3 hours at 7000.
although the organically bonded chlorine disappeared after r-\jll2
hour. The yields were gradually reduced when heating was prolonged.
It is believed that direct alkylation takes place in the initial
30 minutes# following by polyalkylation, overalkylation, interac
tions of and with the by-productsq decomposition andogolymeriza-
tion. Hydrolysis of the AM 3 complexes by water -4 C showed the
presence of considerable amounts of substances of high molecular
weight (,,..,1200), of an unknown structure. Hydrolysis of a iOO g
Card 3/5

274M
P/01 61/'040/008/005/0')8
Reaction of benzene with D233YI)305
portion of the complex with 30 % NaOH yielded Ij42 g of a heavy
steam volatile oil and rJ37 g of a pitch-like residue. The substan-
ces were found to be partly unsaturated and are thought to form by
J
polymerization. The alkylations were carried out by conventional
techniques. Reaction products were separated from the AlC13 -")M-
plexes, washed with 50 % NaOH and then with water, dried over an-
hydrous Na2SO4 and distilled under reduced pressure. An early,
lower boiling fraction and a main fraction containing the aiky!
benzene were obtained in each case. The early fractions were founa
to consist largely of paraffins. The products of the alkylation of
benzene with n-decyl chloride [Abstractor's note-. This should be
In-dodecyll chloride] were sulphonated to ascertain the non-aroma-
tic content* The crude product (after removal of free benzene),
dodecyl benzene and the residues from the distillation of dodecyl
benzene were found to contain respectively 7.2, 4.5 and 27.6 ~- of
compounds which could not be sulphonated. These percentages were
calculated in relation to the total organic matter in the neutral,
Card 4/5

2.71418
P/014/61/040/008/005/OUB
Reaction of benzene with D233/D305
sulphonation mixture. There are 3 figures, 5 tables, and 8 non-
Soviet-bloc references. The reference to the Bnglish-language pub-
lication reads as follows: H. Gilmm , and J. Ture, J. Amo Chem.
Soc., 61, 478p 1939a
ASSOCIATION: Katedra technologii chemicznej organioznejg politech-
niki dllskiej (Department of Organic Chemistry Tech-
nology, Silesia Polytechnic)
SUBMITTED: July 14, 1960
Card 5/5

MOM, Tadeuaz; HOFFINGERp Alfred
Synthesis of alkylbansenes from chlorinated fractiozm of higher
uynthetic bydrocarbDns. Przem chem 40 no.9:509-511 S 161.
1. Katedra Tecbnologii Chomicznej Organicznej, Politeobnika Slaska,
Gliwice.

MAZONS11, Thdousm; GASZTYCH, Dlonizy
lzzz:~
Studies on ths,Okylation of benzene with oleflus In the presence of
almdum abloride. Pt. 2-. Alkylation-of bewAne with propylene and
buty-lene with-the addition of dileoprpylebanzene and dibutylobanzenes.
Przem chem 40-,no.10:571-573 0 161.
1. Katedra Tecbnologii Cbemieznej Organicznej, Politechnika Slaska,
Glivice.

HAZORSKI., Tadeusz,- LACHOWICZ, Alfred; GCRNIAY., Janina
T-
Imediate obtainin of chtnoli derivatives from nitro
compounds, 1, Rooz chemii 36 no.5:873-877 062.
1, Xatedra, Technologii Ghemioznej Organicznejv Politechnika
Slaska., Gliwice,,
Aff

P/014/62/041/003/001/003
D204/D301
AUTHORS: Mazofiski, Tadeusz and Gasztych, Dionizy
TITLE: Studies of the alkylation of benzene with lower olefins
in the presence of AlCI III. Multiple utilization of
AIC13 complexes in alkylaotion and peralkylation reactions
eERIODICAL: Przemysy chemiczny, v. 41, no. 3, 1962t 137-140
TEXT: A summary is first given of the work of Valin et al.t who believes
that complexes of AlCl- with olefins and alkyl benzenes act as a source
of alkyl radicals as All as alkylation catalysts. Following this theory,
the authors wished to establish whether such highly active complexes could
be used repeatedly for the alkylation of benzene with propylene and buty-
lene and for the peralkylation of di-iso-propyl and dibutyl benzenes. Pre-
paration of the olefins and the apparatus were those used earlier. ite-
peated alkylations were performed by decanting from the liquid AIC1 3 Com-
plex layer the alkyl benzenes formed after the first alkylation, adding
Card 1/3

P/014/62/041/003/001/003
Studies of the alkylation D204/D301
fresh benzene to the once-used complex, and starting the reaction again,
without further additions of AICI3 . Other reaction parameters were kept
constant. It was found that high yields of the alkyl benzenes could be
obtained after up to 6 repeated utilizations of the same portion af the
complex; this number could be increased to 8 if small amounts of AlCl 3
or anh. HC1 were added after-a time. Introduction of moisture rapidly
deactivated the catalyst. The proportion of cumene (in the case of pro-
pylene alkylation) tended to increase after the first reaction, going
through a maximum ( - 65%) on the 4th - 5th alkylation, whilst the yield
of polyalkyl benzenes which also formed, increased with successive re-
actions. similar effects were observed with butylence In the case of
peralkylationt The complex may not be re-used more than 3-4 times. The
results are tabulated and briefly discussed. Zofia Solich, a student,
participated in the experimental part of this work. There are 4 tables
and 8 references: 4 soviet~-bloc and 4 non-soviet-bloc. The references to
the gnglish-language publications read as follows: T. Berry and E. Reid,
Card 2/3

P/014/62/041/003/001/003
Studies of the alkylation ... D204/D301
J. Am. Chem. Sec., 49, 3142, (1927)'; Canadian Pat., 265,521, (1926).
ASSOCIATION: Katedra technologii chemicznoj politechniki Sleakiej '
(Department of Chemical Technology of the Silesia Polytechnic
Institute) -
SUBMITTED: July 26, 1961
Card 3/3

MAZONSKIj, Thdeuez; GASZTYCH., Dioni2y; ZIELINSKI, Wojcieeb
-- - -- .-- -- .--. -
Nydrwqlation of allyl alcohol with hydrogen peroxide to glycerine
in the preoence of pbosphotungstic acid. Px-jm chem 41 noo'5:251-
254 W 162.
I* Katedra. Technologii Cbemicznej Organicznejp PolitechnDm 31-ska,
Mivice i Instytut Ciezkiej Syntezy Organicznej Blachowta, Slaska.

JABLONXA, Stanislaw; MAZONSFJ., Tadeusz; TANIEWSKI~ Marian
Comparative studies on pyrolysis of normal heptane, octane
decane, and dodecane in a tubular reactor. Frzem chew. 41
n0-5:254-256. My 162.
1. Katedra Technologii Chemicznej Organicznej, Politechnika Slaska,
('liwice.

Ma Tadeusz; KULICKI, Zdzielaw; FIADUR, Brygida
-'-'q]PWj
Reaction of alkylating chlorobenzeno vith isopropyl alcohol in
the presence of various catalysts. Ptl. Rocz chemii 37 no.5:
569-573 163.
L Department of Organic Technology, Silesian Institute of
Technology., Glivice.

-ACCESSION NR: ATL-001531 P/2517/63/000/085/003/0010
AUTHOR: Mazonski
Tadeusz; Gasztych, Dionizy
TITLE: Stuaes of the utilization of distillation residues obtained in the
production of ethylbenzene
SOURCE: Gliwice'* Politechnika Slaska, Zeszyty naukowe., no* 85, 1963., 3-10
TOPIC TAGS: benzene.ethyl r aikylation,, distillatien, distillation residue,,
bottom, residuum,,, mazout, benzene derivative.,-ethylbenzene
-ABSTRACT: The distillation residues constituting the by-product of the synthesis
of ethylbenzene contain substantial amounts of polyawi~enzenes which can be ut-
ilized as-a source of alli*1 radicals in the production of ethylbenzenes. The term
"polyethylbenzenes" commonly applied to this by-product is a. misnomerp however.,
because of the.presence of large quantities of other chemical compounds whose phy-
those of such hydrocar
sical pro~perties resemb bons ~s dipheny1j. diphenylethane.,
etco These compounds predominate particularly in,thq high-boi3ing fractions. The
above distillation residues (a more correct te=) maX be used as the starting
material for the' production of ethylbenzene aftera preliminary fractional dis-
~.~ard 1/2

~.'.A.CCESSIOM M. AT4001531
tillatione Comwrcially Interesting gields of ethylbenzene can be obtained from
the product distilledup to about 100 atl5mm'Hg. Highvr-boiling products
should be used for other purposes because of their =all content of polyalkyl-
.benzenes* Preliminary refining of the product is not necessary And not recommend-
ed, because the rufirUng process causes a loss ~,of the. product., and the yields of
.ethylbentene obtained by -reoaLkylating the product of rofid;ig are lower than in
.-the case of the unrefined product* Ori~e article has 3 tables*
w
:.-ASSOCIATIONt Katedra Technologii Chemicznej OrganiczneJ (dhair for the
Organization -of the Chemical Indus
try)
'SUOUTTO: ..00 DATE ACQ: 2 CDec63. ENCL: 00
w
v
NO REF SOV:* 000'
SUB CODE: CH OTHER: 002
.:..:!Cara 2/2

M=SKI 17
.vadrusm; BIEIWKI, Piatr.
-11.~-,~-~,~~---,.
PbOOS-bUitisa of certaft synthaseq of o-nitroathylbanzAme.
Pt&2. Roes chemii 36 no.7/63-155-1158 162.
I* Tatedra Technologii Chamicznej Organioznejv Politechnika,
Miwice.

MAZONSKIJ, Tadeusz; HEIIN, Zygmunt; Alfred
A3kylation of aromatic hydrocarbons with halogen alkanes in
the presence of metallic aluminum in the liquid-vapor phase.
Chemia stosow 7 no.3:393-399 163.
1. Katedra Teciinologii Chen-lezncj Organicznej, Poltechnika,
Gliwice.

KARIUNSKI, Wladyslaw; KULICKI, Zdzislaw; MAZONSKI, Tadeusa
Poe-ibilAty of separating poeudocumene from solvent
petroleum by fractional distillation and selective
sulfonation and desulfonation. Koks 9 no-W22-126
J1-Ag 164.
'0'
1. Department of Technology of Organic Chemistry of the
Silesian Technical University, Mwice.

JAWORSKI, Jerzy; MAWNSKI, Tadeusz
Studies on the chlorination reaction In the bextichlorobenzens
preparation process. Przem chem 43 no. 2: 92-9,4 F 164.
2. Katedra Tacbnologii Chemicznej Organlcznej, Politechnika
Slaska, Gliwice I Zaklad nauknwo Badawczy, Zaklady Chemiczne,
Oswiecim.

L 36901
ACC NRs
RM
5OURCE CODE:
AUTHOR: Kardnska, Barbara; Mazonski, Tadousz 2,q
ORG: Department of Chemical Organic lochnoloE7, Po chnic, Gliir~ce U
Technologii Chomicznej Organicznoj Politechniki Slasicie j)
TITIZ: Derivativos of Ljmgrq_nthene~ I. 4-acetylairdno-11-bromofluoranti-teno and
3-1-bromofluoranthene
SOURCE: Roczniki chezdi - annales societatis chimicao polonoram, v. 40, no. 1,
1966, 65-72
TOPIC TAGS: bromination, chemical reduction, solubility, isorwr
ABSTRACT: 4-acetaminofluoranthene has been shown to undergo bromination in posit ':.Lon
11 in the mixture acetic acid-carbon tetrachloride. New fluoranthono compounds are
reportedt 4-acetamido-, 4-amino-U-bror-iofluorantl,-.ene, and 22-bromofluoranthene.
Differential solubility in ethanol and different susceptibility of the individual
fluorantheno rings to reduction were utilized for iaomor separation. 9!~~G~rodzkq,
Ewa 11iron. Anna Horoszko and RozaUa Wadr k art'Icipated 1n the experimont. Orig.
art. h.-:: 1 forrmla. sed on au ors , ng. abstj D-PRS: 35,39ff
SUB CODE: 07 / SUER-1 DAM: 07Jun65 / OTH REF: 009
1~s

-)-- T?M
SOURCE CODE: PO/0099/66/040/003/Q499/0501
AUTHOR: Kulielal, Zdzislaw; Kiersznicki, Tadeusz; Mazonski, Tadeusz --2 K,
ORG: Department of Organic Chemical Technology,, Silesian Institute of Technology,
Gliwice (Katedra Technologii Chemicznej Organicznej PolitechnikkMaTIM" I
TITIE: Alkylation of chlorobenzenj by isopropyl bromide in the presence of anhydrous
aluminium chloride catalys-f-
SOURCE: Roczniki chemii-annales societatis chimicae polonorun, v. 40, no. 3, 1966,
499-501
TOPIC TAGS: alkylation, chlorobenzene, isomer
ABSTRACT: The alkylation of chlorobenzene with isopropyl bromide in the presence of
anhydrous aluminum chloride has been studied. The-content-ot-wthop-meta, and para-
isomers in the mono-isopropylc lorobenzen fraction has been detemined. The yield
a as 68.6 percent,, the orientation obtained was
of mono-is2K2U1,chlordbenzen P~
approximately 10.0 percent ort o,, 65-4 peftent meta,, and 24-4 percent para. The
analysia of the oduct was performed by vapor-liqaid chronatopgraphy. Orig. art.
Ihas: 1 table. ed on axthors' Engs abstel [JMS: 36,,002J
'SUB CODE: 07 / SUBM DATE: 13"5 / CRIG MEN - 001 SOV MW: OQY

_67
IMP( ---- -- IRV

AmVd. mw to
'v DIP92ft"
POlltedWkl.SUSklej
ce

46-saw A07_0 i~66i_ '15c)94u

Opr Iq "d diiiii3i oveltroculivii

Ung
prowlquindi ~9' 46d 643 0 UiA
:d,"!" U doicri 0-
$u th
- ~
MIN
---

Io
quin
'4ticn
Iva Ive ..
tm2i&c.vn=lc'~d*r t ....
OthOt
ORIC - 007,

410

ZITADULIATAT. S.K.; KaOR,_,.A.B., red.; UMSKIY, P.A., takhn.red.
[Important problems of construction and reclamation in the
Golodnaya Steppe] Vazhneishie voprosy strottelletva i
oevoonlia Golodnoi stepi. Tashkent, Got. izd-vo Usbakskol
SSR, 1937. 34 p. (HIRA 12t2)
1. Chlon-korrespondeAt Ak9demII stroltalletva i arkhitaktury
SSSR (for Zlyedullayer).
(Golodnaya Steppe--Construction Induatry)

&ZOR, B. S. , tekbuft
Interlocked switcb control by mans of a noureversing aoc.
drive. Ugoll Ukr. 4 w.405-36 Ap 060. (MIRA 13$8)
1. Lupmakproyekt,
(Blectricity In mining)
(Mine railroads)

HAZOR~ D. N.
FAZUR, D. N. -- "Classification of Fresh Gunshot Wounds of the Skull and Its
Contents and Certain Problems of the Surgical Tactics to Be Used in
Treating Them." Sub 15 Apr 52, Central Inst for the Advanced Training
of Physicians. (Dissertation for the Degree of Candidate in Medical
Sciences.)
Sr;: Vechernaya Moskva January-December 1952

i J-V
'3 Pp
Q-1 t1w yellluiv n
raillmitlEttted "I
alluntitv of tile 1
Nit.
. "Niuaftw,
Jium phusplimmilylida. v
It vilun twuld litnt by-decromitiK-tho
1;1 ~ldc -63 UPW i i
tl e gellslilvity of tile

AssalpAs of W4 and magovem sk*sb. I hal Mhvw.
maqcp Khm. LAP, 14. &W-1009411).-Tbt - --litsPi-
jup r= tool mer samples b rude ea3da =4 bested
to SDO~-"' and cooW Aawly. The bat Wrent b 8 N
HCJ aW water widmt any btstbS. Is b ma advkabSt to
&W HN%. DeldW dbectsom we Siva for dttg. W,
us, Cy, V. U% hl, Co. 01. 71. WA At. The deta. of the PC
Mtftt Mrm as 4 contro; to chn-h lb, tiplimbulty W the
vwuts. I - Pidly

L. MAZO-i. L. ERDEY.
"Mass-analitical determination of van.adine with kaliumperiodate" P. 331
(ACTA CHMICA ACADENIAE SCIENTIARUI-I HUND.WRICAE, Vol. 2, no. 4, 1252,
Budapest, Hungary)
-01
SO: Monthly List Gf East z;uropean Accessions, L.C., Vol. 2 No.7, July 1~63,Uncl.

MAZOR, L.
"Determination of Vanadium by Oxidizing the Heauating Solution. " Pt. 2. p. 469, %dapest,
Vol. 3. no. 4, 1953.
SO: lkst Baropean Accessions List, Vol. 3, No. 9. September 1954. Lib. of CongresB

GDO Do
'
_1L Erd X aa&
BiLam w e
layo

f unt- Standard - :m tboV or_70
,h
iku *1, v A ImMftr: Al- anil - Al -WI6
-
-
-
h di~ -
hi
-
w
r
c
n
q 611
,V
,
Zyl=
10" P_
_
'i'' T'..
'C-M
Nnj)r~ Od hy -A 2 t1
10''
-14
so
~.
i
i v
_

ftrs-
pt!r,
rT1iimT. b e df hc)
ihethnd h :kIbi If
dc cliwnal- _V'in
t
or

-d
u
mewaild Itho
-
.'
.
l
d
i

S
o
ino xncth'A
nqqtat
ZAI;I%o
I .lie
Md -lar tbo
Y
'

- V
or-, Ili OAV
dcomaiftaffor ~W
Wa-~ djp1141tIAo6i

by
ha
'
-
v4,
RCI f siliarillua
ii adjust
V - d!cWyItbJociwbamrmtc complex is
pre
-6
_*
~-
l
Th

rm
cicls dccompos
t
d by. a maxtilre of
mp
'v sta
lils-6 aiid If'o'. "a the t 116eiit~d 13 iT
-V
an- a Tho' oi;~
salution

-

th
e
7 _7
-
aAd
ia
d
f J
ove
tid
zee
i
less- Thus the zl~ O
,
_
*
V salt. in a vo'--~
hssibU tb'di
zii0iia
fh6
y ~be p
'Appro -1D
prlai. to -tha quantity, Uv 'racnt
xactric det~rmiuatiou - o1
'bdoplip
IsIihma Or tunisltvabv~zto*
;i. ro3m v ium t6m
or, Is ibaw
V

~~

MAZOR, L.
lasmio Szekeres I AtIalanos kesda (General 'Chemistry); a book review. p. '425
)bgyar Kemikusok IApja. Vol. 10, no. 10, Oct. 193y-
Source: East European Accessions List,(EEAL), Lc- Vol. 5, No. 2, Feb. 1956

A~ 2;",1. ne 4L--d
thAt co6taia F gives high
Telltalts. M= ~ny'IfF wl6ch is forawl reaqts with
'on tubc 0 glide water.
.io-siUcx-q the xxjrribuslt
Thi Lai
Co.
0--ovelOorOD AIMS a-. IZr-.Ol
insition-Wiffi ~OvWmool i's

z.--
AW
Mild
man
via=$
1957i'.N
imp ve
ig Pon zmwu 16,
-tw tbt
1)y
f
be-d=loow
forkber I
ly -0 wts,
-aa
No IMIS An
tou
tu

ar
;,nal---tic.-I Cher-ctry i,,,,,jy!3jF of Or:
J.~
'A -"D: J/t

YAZOR, L.; MEISEL, T.; ERDF",, L.
Data on the microdetermination of the sulfur content in organic nompol,nds. p.04.
MAGYAR KEEITTYUSOK UNA. (Mag-jar Kemilmook EF~iesvlete) Budap-ent, Hungarv.
Vol. 24, no. 12, Dec. 1959.
Monthly List of East European Accessions. (PFAT) LC Vol. 9, no. 2,
Feb. 1960 Uncl.

, M xiai tudomMok kandidatusa
~AIOR ~~~
Now trends and achievements in the organic chemical analysis; a
contribution to the accoant by the Section9s leadership. Ken tud
kozl NTA 14 no.2:233-238 960. (EUI 10:2)
(Rangary-Chwdetry, Organic)

VEIBEL, Stig- MAZOR lasslo [translator]
Significance of the group 4nalysis.of organic conpounds in research
and teaching. Km.*-tud-iwzj-'XU l6 no.4:)97-/,05 161.
1. Organisch-chemisches Laboratorium der Technivehen Universitat,
Kopenhagen.
(Organic compounds)

HAM
An aceount of the Congress of Analytical Chemintrye Ylag7 kem lap
16 no.6:291-292 Je 161.
I..wXagyar Kemikusok Lapja" szorkeszto bi2ottsagi tag.

,=CH,, L.
9&thodo of organic elem3bntal microanalysism by 0._Tngram.
Reviewed by 1.9 Mazor. Periodica polteelm chem 6 no.4:261-
262 662.

JMEML, Tibar;,,- jamlo
1-- "1.
Process for detexulng phoagene. Yka ken lap 17 no,9:421"423 S 162,
I* Bobapstl Mnazaki Egyetem Alta.Unov Kemisd Tanozek. 2. 'Magyar
Kemikuook LapjO, szorkeezto bimettsizi tagja (for Hazor).

M=M, L.
ImAmlytAc chemistry of organic compoundes by Stig Voibele
Reviewed by L. Hamor. Acta ehimica Hung 37 no,3t348-349 163.

"I
IIAZOR, Laszlo, dr.
An account of the conference on analytic chemistry. Magy kem
lap 19 no. 3tl7O Mx 164.
1. Editorial board member, I'Magyar Kemikusok Lapja.11

MAZOR, Laszlo, a kemiai tudomanyok kandidatusa
Present state of organic chemical analysis in Hungary and abroad.
Kem tud kozl MTA 21 no. 4:375-383 164.
1. Chair of General Chemistry, Budapest Technical University.
.or -19

MAZOR, Laszlo
An account of the 1964 Conference of Chemists. Magy kem lap 19
no. 12:674 D 164.
1. Editorial Board Member, "Magyar Kemikusok Lapja.11

MJAMI~OR., S.W., inzh.
Efficiency of the one-phase method for regulating the power and
qeicing of UO kv. power transmission lines. Elek. eta-32
161. (MIRA 14:5)
5:9446
no.
My -
(Electric pover distribution)

MOOR, Yet. 1.
Oatsoarticular tubercullosis and the eye. Probl. tuberk., Moskva No.6:
66-67 Nov-Doc 51. OLML 21:4)
1. Of the Clinic for Eye Diseasse (Director-Prof* H#I. Hedvedev),
Crimean Medical Institute imeni I.V. Stalin (Direator-Docent V.I.
Larin) and of the Administration of Yevpatorlya Health Recort
(Director-P.V. Gremitskiy)o

)Won, Yu. . inab. (Riga)
The mA :24-27
.umaw mdjo receiver. Radio noo7
ji 62.
(MIFLA 16.- 6)
(Radio-Receivers and recePtiOn)

107-57-2-39/56
AUTHOR: Mazor and Ratiner, L.
!2!~~
TITIX: IlLyuka" Rad',io-Phonograph Combination (Radiola "Lyuks")
PERIODICALt Radio, 1957,1hir 2, pp 39-41 (USSR)
ABSTBACTt The Riga electrical manufacturing plant "VEF" has developed,
and is putting into mass production, a new radio.-phonograph combination
"Lyuka" (RK-156) that has a VIEF band. The Lyuks is an 11-tube ~uper-
heterodyne AM and F11 radio receiver combined with a universal record
player. Chassis, subassemblies, and parts of the new radio-phonograph
are standard; they are used at other plants of the Ministry of Radio-
Engineering Industry. Lyuks has a 110-p 127-, or 220-v AC power supply.
It weighs 27 kg, and its dimensions are 625 x 450 x 365 mm. Consumption
is 85w f or radio and 100~r f or both radio and record player. Six wavebands
are provided: long waves, 150 to 415 kc,medium waves, 520 to 1,600 kc~
short waves, 3.95 to 5.5 mc, 5.2 to 7.5 me, and 9.4 to 13.0 me; and VHF,
64.5 to 73 mc. Intermediate frequenq for the AM section is 465 kc;
for the F11 section, over 180 kc. Sens *itivity at the 50-mw output is
20 to 50 &v for long, medium, and short waves, and 5 to 10(av for VIIF
(at 300-ohm input). The sensitivity for long and medium waves with an
internal magnetic antenna is 5 to 10 mv, Adjacent-channel selectiiqtv
Card 1/2

"Lyuks" Radio-Phonograph Combination
107-57-2-39/56
for the AM section is over 60 db within ~10 kc; for the FM section, it
is over 30 db within 1250 kc. Heterodyne frequency voltage on VHF antenna
terminals (at an input resistance of 300 ohms) is 40 mv or less. With
the input voltage change of 60 dbt the AGC insures a change in output voltage
of 9 db for the AM channel, and of 16 db for 'the FM channel. The rated out-
put is 6 v&, and the maximilm output is 8 to 9 va. Distortion is within
5% to 7%. The volume can be controlled within 60 to 70 db. Separate tone
controls are provided. Background output is 50 to 60 db lower than the
rated useful-signal output. The fidelity curve has about a 14 db variation
between 60 and 12,000 cps. A part of the AM tubes is also used for Fif
reception. One 6N3P, three 6K4P, one 611r, one 6102P, two 6N2P, tvo 6P14P,
and one MS tubes are used in the radio-phonograph combination. A
complete circuit diagram is presented and explained in detail in the
article.
There are 2 figures in the article.
AVAILABLE: Library of Congress
Card 2/2

107-57-4-16/54
.AUTHOR-. -Mazor, Yu., and Ratiner, L.
TITLE: Radio -Phonograph Combination "LyukB" (Radiola "Lyuks")
PERIODICAL: Radio, 1957, Nr 4, pp 19-21 (USSR)
ABSTRACT: A detailed description of the construction and principal data of vari-
ous sub-assemblies of the "Lyuks" radio -phonograph combination are presented.
The circuit diagram and other data were published in "Radio, " 1957, Nr 2.
"Lyuks" and "Kontsert" radio -phonographs use the standard parts. A
keyboard-type switch and a high-frequency unit are mounted in the center of the
chassis. Placement of the other parts is described, and the advantages of the de-
pWare discussed. The keyboard switch controls the various hf bands, the
record player, and power supply. Type EPU- I 11 record player has two speeds
(33-1/3 and 78 rpm) and is driven by a 12-watt motor. Frequency response of
the record phiyer is 75 to 7,000 cps. Its distortion is 3-5%, and sensitivity
50-70 mv/cm/sec. The speaker system of the radio -phonograph combination
consists of two 5-watt 5GD-14 wide-frequency range loudspeakers facing the
front wall and two elliptic type 1GD-9 1-watt tweeters facing the side walls of
the cabinet. The combined frequency range of the loudspeakers is 50 to
Card 1/2

107-57-4-16154
Radio -Phonograph Combination "Lyukell
12,000 cps. Detailed parts data, a table and instructions for winding coils and
transformers, and coil dimensions are given in the article..
There are four figures, one table, and one Soviet refereno* in the article.
Card 2/2

107-57-4-17154
AUTHOR: Mazor, Yu., and Alekseyev, V.
TITLE: External fte&ker. Systems (Vynesennyye akusticheskiye sistemy)
PERIODICAL: Radio, 1957, Nr 4, p 22 (USSR)
ABSTRACT: Designing and developing the "Lyuks" radio -phonograph combination
has shown that it is hardly practical to combine high-power loudspeakers with
a small-size variable capacitor, a record player, and other parts susceptible
to microphonic effect. improvement it the quality of reception and sound, vhile
simultaneously cutting down the size and weight of the apparatus, cannot be
practically achieved with one-cabinet construction. A two-cabinet system is
suggested by the authors, in which one cabinet would house the receiver, first
stages of the a-f amplifier, and the record player, while the second cabinet
would house the loudspeakers, power supply, and final stages. The shape and
size of the second cabinet would be determined only by acoustical considera-
tions. Advantages and disadvantages of the two-cabinet system are discussed.
The system is claimed to be practically applicable to higher -c:lass, more ex-
pensive radio -phonograph combinations.
Card 111

6(4)
SOV/107-58-12-23/55
AUTHOR:
TITLE: The "Lyuks-2" Radio-Phonograph
(Radiola "Lyuks-2")
PERIO,ReCAL: Radio, 1958, Nr 129 P 17 (USSR)
ABSTRACT: The author briefly describes the "Lyuks-2"
radio-phonograph, produced by the "VEF" plant,
which is an improved version of the "Lyuks"
model. The most essential alterations have
been made to the VHF unit, as a result of which
the radiation voltage at the antenna termi-
nals is 20mv and the warm-up drift is 10-40 kv
per hr, 5 mins after switching on. The trans-
mission band of the i-f frequency modulation
channel has been narrowed to 140-160 kc; in
the three stages of the i-f frequency modula-
tion amplifier a system of grid limiting is
used instead cf AGC. The fractional detector
Card 112 system has been improved by reducing the load

The "LyukB-211 Radio-Phonograph SOV/107-58-12-23/55
resistance to 15 kilohms, correct selection
of the relationships of the phase inverter
transformer and special means of balancing
the circuit. The short-wave (KV) band has
been spread (KV1 - 9.36 to 12.1 mc KV11 -
5.9 to 7.4 mc, U111 - 3.95 to 5.9 mc); in
the i-f AM channel the selectivity and form
of the resonance characteristics have been
improved, and the design of the coils simpli-
fied.
Card 212

HLZOR.. Yu.L.
Concerning certain relationship of an PH discriminator with
series connected rectifiers having a comon dace loop*
Radiotekhnika 16 no.8:54-57 Ag 161e (MIR& 34:7)
1, Deystvitel'W ch2en Nauchno-tekhnicheskogo obshchestva
radiotekhniki i elektroov7azi.
(Radio filters) (Frequency regulation)

MEOR, Yu.R.
Metamorphism of Norillsk coals. Izv. vys. ucheb. sav.; geol. i
razv. 1 no.4:52-67 Ap 158. (MIRL 11: 12)
loMoskovskly geologorazvedochnyy inst1tut imeni S. Ordzhonikidze.
Kafedra goryuchikh iskopayeuVkh.
(Noril'sk region--Coal geology)

MAZOR, Yu. R.: Master Geolog-l-lineralog Sci (diss) -- "Geological factors in
----WW"xO
the metamorphism of the coals of the Nori'sk coal region". Moscow, 1959. 19 pp
(Min Higher Educ USSR, Moscow Geological Prospecting Inst Lm S. Ordzhonikidze),
110 copies (KL, No 9, 1959, 113)

MATVEYEV,, A.K.) MARTYNOV, YS.G,j HAZORp YU*R*
Zonality of contact netamorphism in coal. Dokl*AN MR 137 no.6.-
U34-206 Ap 161. (MM 24:4)
1. Mskovokiy goeudaretvennyy univermitet imsul M.V.Lomonoeova.
Predstavleno, skademikom W.M.Strakhovymo
(coal &ology) (Metamorphism (Geology))

TUMASHEVA, N.I., dotBant; J=-&M
PSYUK, S*K,; CHAYKA, X.L.-
SIIVARTSBURD,, A*86
Antistreptolysin d an-tihyaluronidase and cutanec;us.reactions to
antigens in puorla,,jis and lupus ex7thematoo-ase. Vast, derm. i ven.
38 iio.7:17-21 Jl 164. (MIRA 1814)
1. Kafedra dermatologAl (zav. dotsent N.I.Tum--sheva) Vinnitakogo
meditsinskogo instituta.
~04~0

mamov, S.
$otter utilization of trackB. Avt.transp. 32 no.9:8 S 154.
(Km 7:11)
1. Samestitell upravlyayushchego Kiyevsklm avtotrestom *SoyuzWottrans".
(Trans-Dortation, Automotive)

MOROV.Ya., inzhener
Nxperience in organizing the work of track fleets on virgin
lands. *vt.transp-33 no.6:11-12 Je '55. (MLIRA 8:10)
(Altai Territory-Transportation, Automotive)

.MAZOW)V, Ta.. Inzbener.
,Centralize the haulage of farm produce. Avt. tranaP. 34
no.6:8-10 Je '56. (MLRA 9-9)
(Farm produce--Transportation)

S L SITALIM"IM WERATift
it AD M
0.4 a 0 0 O's 0-a-6
16 &,'-o
-w0
I f -041
Znee
=00
goo
off
Me*
Nee
too
Nee
too*
goo
'Ir Im 0 a 0 1 w a 9 a a 9 v
a*

0 IS 0 9 ~v mv-0 let #**40104 4 a
4;4) AS or*
0 1 -1 -Ad
it, ..0 fp ~'vvsws k,
at ..v #ASAIRfq% .,.A
IS
so The rab of abowlMem d ex w by 99alim. A. 16'. -00
so _J. Chm. Ind. (U. S. U.) 15. No. 7. 32
CA=d. alk. p)togaUPI MAI's. atamit 0 fastrr
Z than by&oswfitc KAM. and much 1"CT than mulmon6cal
'r cucl sulla. .00
Z egos
0 0 13 zoo
z0
ago
Coo
;a**
wool
A IS - I L A RITALLURCICAL UTINIATIS111 CLASWKATICM
101142 Cl- Q-1 a ISO I (w 0.1
-a- ad 0 it 0
u n AT 10 0;0 #30
14D & o 0 v 41
Ads
is 0 0 0 0 0 0 0 a 0 0
0000 000 *of 6*0