SCIENTIFIC ABSTRACT LUBRICI, C. - LUBYANOV, I.P.

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• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001030710012-6
• Release Decision: RIF
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• Document Creation Date: November 2, 2016
• Document Release Date: April 3, 2001
• Sequence Number: 12
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

G16-
SWULAMS (in ca;o)4, Given Names
Country: Rumani a
Academic Degrees:
A'fillt~tion: Rose eri-
-grch Centqr,._tQr Bacterial V rtilizers (Centrul Exp
mental do Ingrasaminte Naoteriene
Source: Bucharest I Sti-inta si Tohnica , No 7 , Jul 1961, pp 26-27.
Data; "How the-*Edible Mushroom" Myoelium Is Obtained."
Authors:
MULTEESCU, N., Chief Researohei- (Ceroetor Principal*)
LIJ BR C.', Researcher (Corootor).

MATEESCU P N. , cercetator principal; LUBRICI, C. , cercetator
How the micelle of esculent mushroomB can be obtained. St sl Teh
Buc 13 no.7:26-27 JI 161.

ACC NKI AT6019b32 SOURCE CODE: ii~/3174/64/000/050/002.4/0027
- (Junior
TAUTHOR: Lubroyin,--L andidateof geographical sciences); ~Impnov.,
research'a-so"C"i"ate)
/
ORG: Arctic and Antarctic Research Institute (Arkticheskiy I antarktiche~kiy
i. nauchno-isaledovatellsIqy institut)
TITLE: -tides in the reiton of the Novolazarevskaya station,,,,,
8OURCE: Sovetskaya antarkticheskaya ekspeditslya, 1955-. Informatsionnyy byulleten', no.
50, 1964, 2.4-27
WPIC TAGS: ocean tide, i~ntarctic climate, sea tee / Z-17 &--,',U 91
'ABSTRACT: The fluctuation of the sea level at the No V azarevskaya. station was observed be-
tween January 10 and February 5, 1963. A MarlUANvas used to record the height of the tide
The observations were carried out at 1 lim north of the station, in L4gernyy Bay, a frcsh-wate~
basin on the northern edge of the Schirmacher Ponds. The bay Is separated from the open so
by the lee shelf about 80 kin wide. The marigraph was installed on Ice 2.5 m thick at a d1st4qj
A
of 50 m from the shore. The depth at the observational place was 25 m. By comparing the
fluctuations of sea level In the open sea and in the bays in the region of the station it was foun~V~7
Card 1/2

t cz
ACC NR: AT6019032
~'Iat the character of the tides does not substantially differ, therefore the authors assert it
the bays situated along the northern edge of the Schirmacher Ponds and separated from the sea
by the wide ice shelf freely communicate with the sea. Thus, appreciable areas of the ice
shelf are floating. The depth of the sea~~'Qer the shelf is rather appreciable, which was con
firmed by data of a geomagnetic survey performed in 1963. Orig. art. has: I table and 3
figures.
SUB CODE: 08/ SUBM DATE: 06May64/ ORIG REF: 004
kh

MACHONj Jozefj inz; GEBICKI, Zbigniew, mgrop inz*; CIRYLOWSKII Jerzy, inz.;
MATYSZCZAK, Stanislaw; KALUZNY, Jan; SKAISKI., Jan; PROM, Leon;
37RUVOWICZ, Wieslaw,, inz.;_JjQaEEZL Czeslay, mecho
Works distinguished and rewarded in the 5th General Polish Competition
in the field of saving electric power. Erergetyka przem 10 no.4:146-
1" Ap 162.
1. Zaklady Azotowe im. P. Findera, Chorzow (for Machon).
2. Przemysl Weglowyq Gliwice (for Gebicki). 50. Fabryka Sprzetu
Elektrotechnicznego, Szczecin- (for Cyrylowski and Matyszczak).

LUBSANOV D D spets.red.; ZILOTIN, Yu.V., red.; RATOTSYRENOVA,
tekhn. red.
(The 40th anniversary of the Buryat A.S.S.R.; articles]
Sorok let Buriatskoi ASSR; sbornik statei. Ulan-Ude,
Buriatskoe knizhnoe Izd-vo, 1963. 137 p.
(MIRA 16:11)
(Buryat A.S.S.R.-Economic conditions)

6--vol 11/? Intf-mal Led. Jiily ~Q
RX-110PTA rDICA see
3803, RADIOACTIVE IODINE IN TREATNiENT OF THYROTOXICOSES
(Ruasian text) - L u b a k a y a 1. 1. PROBL. ENDOKR. 1958. 413 (93 -98)
Tables 4
Data on treatment of 15 patients are presented, Out of there, 37 patients suffered
from grave thyrotoxicoeis and 120 from thyroloxicasis of average severity. The total
duse of Iodine per course of treatment varied f rom 2 to I I mc. and was adm inistered
In 2-3 doses with an interval of 5-6 clays: 138 patients received one course of treatment,
IS patients 2 courses and one patient 3 courses. As a resuLt of this treatment re-
mission or a considerable improvement took place in 85.3% of patients (the pa-
tients were followed up for 3 to 14 months). Improvement was noted in 697o of
cases at the end of the first month after treatment, while in 17% of patients positi-
ve results appeared only in 3 monthb and even later. Insignificant improvement
was found In 10 patients, absence of any effect in 3 and symptoms of hypothyroid-
Ism in 2. After treatment with radioactive Iodine (1131) a temporary exacerbation
ofthyrotoxicosis, requiring special therapy, was noted in I 11%of cases and a reduced
number of leucocytes in 32%. Temporary thrombocytopenia was noted In 50% of
cases. Administration of 'cortin' makes It possible (to a certain extent) to prevent
the appearance of leucopenia and thrombocytopenia. (VI, 3. 14)

LUBSKIY, I.
Radio Clubs
With the members of the All-Union Voluntary Society for Assistance to the Army,
Aviation and Navy at the Voikov Secondary School. Radio No. 4, 1953.
Monthly List of Russian Accessions, Library of Congress, June 1953. Uncl.

IVBSKIY, I. (g. Boykovo, Berezanskogo rayona, Kiyevskogo oblusti).
Why doult we have transformer colls? RucLio no.9:16 s '53. (mTRA 6:8)
(Radio-Transformers)

LUBSKIY, I. (Voykovo. liyevskoy oblasti).
Rearrangement of the wRodina-479 receiver's output stage. Radio no.10:55 0
15). (HUU 6:10)
(Radio--Repairing)

SLISKOVIC . T LUBURIC t P.
Stratigraphic aspects of bauxite in Hercegovina and southwest
Bosnia. Bul-sc Youg 9 no.1/2t6-7 F-Ap 164.
1. National Museum of Bosnia and Hercegovina, Sarajevo (for Sliskovic).
2s Geplogio and Paleontological Institute, University of Zagreb
(for Lubaric),

PAPESI J.; LUBURIC, P.; SLISKOVIC, T.; RAJIC, V.
Geclb~ic ralAtionii of'th6-wid6r environs of Livno, Davno, ind
Glamoc.in southwestern Boania. Geol glas BiH 9s87-122 164.
1. Submitted June 11, 1964.

MUFTIC, Mineta; LUBURIC, Petar
Lithostratigrt!phic and tectonic relations of the Uoustrine
Neogene'in Bosnia and Herpegovina. Ge6l glag BJH ?t103-130 163.

SLISKOVIC, Teofil; PAPES., Josip; RAIC, Vidj LUBURIC Pero
Stratigraphy and tectonics of Southern Hercegovim, Geol glas
Bill no.6:LII-J-40 162o

L v 6 C, /i (~~ (7, V /I
RUMANIA/Magaetism - Ferrites F-6
Abs Jour : Ref Zhur - Fizikaj, No 3., 1958,, No 6136
Author : Lubusca Elena., Constantinescu Florica
Inst '-Yo-t-GTVWr'
Title Variation of Magnetic Properties of Mixed Ferrites Cu NJ as
a Function of the Cu/Ni Ihtio
Orig Pub Comun. Aced. M., 1957., 7o No 4., 413-420
Abstract Starting with the nickel ferrite of the type NiFe 204'ZnFe2O4
which is characterized by very low losses at high frequency
current., and from the ferrite of copper of the type CuFe2P4'
ZnFe204,P which is characterized by high permeability., the
authors have developed a series of mixed magnetic farrites
of the type NiFe2O4'CuFe2o4'ZuFe2o4 and have established
the variation of the magnetic properties (,U, tan 6 )
as functions of the copper ferrite to nickel ferrite ratio.
Card 1/1

LEMMA, A.
LUBUSKA, A. Thermomagnotic investigations of the phenomena occurring during the
heatirg of hardened steel of the NC4 tYPe- Blulet - P-6 45
Vol. 23, no. 12, Dec. 1956
HUTNIK
FOLI-.IC-.',,L 6G--,Z:CE
Narszav,la, Poland
So: East -European Accessicn. Vol. 4, No. 3, Yarch 1957

L . Adam
W 9-00-02~
Strain hardening of bainite, Mechanika Gliwice no.16:
43-47 162.
I* Instvtut Metalurgii Zelaza i Katedra Metalomiawstua.,
Politechnika, Gliwicp.

LUBUSKA, Adam Zbigniew, dar inz.
Gauses of the differences of the relation value P ,/R
in construction steels isothermically hardened PQ r
thermally improved. Przegl mach 22 no.21:672 lo 11 k63.
1. Katedra Metaloznawstwa, Politechnika, Gliwice.

86498
S/07Y6 0/03 0/011/003/02 6
B001 Bo66
/C~)
AUTHORSt Nikishin, G. I., Voroblyev, V. D.# and Lubuzh, Ye. Do
TITLE: Physical Properties of 1,4-Dialkyl Cyclohexanes
PERIODICAL: Zhurnal obahchey khimii, 1960, Vol- 30, No- 11,
pp. 3548-3554
TEXT: The authors synthesized in a previous study (Ref. 1) 1,4-dialkyl
benzenes according to the scheme
R-//
Br \,Z13r..4,-21ig + 2RBr -R + 2MgBr
(R - normal alkyl radicals 0 4 U9 They hydrogenated in the present
study p-dialkyl benzenes, and studied some physical properties of the
resultant 1,4-dialkyl cyclohexanes hitherto unknown. Hydrogenation was
conducted in a rotating autoclave at 210-2300C, at aninitial pressure of
110-130 atm, by means of a nickel catalyst; their separation was carried
out chromatographically. After purification on a column filled with
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86498
Physical Properties of 1,4-Dialkyl S/079/60/030/011/003/026
Cyclohexanes B001/B066
silica gel, the resultant dihoxyl-, diheptyl-, dioctyl-, and dinonyl
cyclohexanes were recrystallized from alcohol. The melting points of
dihexyl- and diheptyl cyolohexanes were determined at a constant tempera-
ture of 0-20C (Table 1). This table also compares the properties of the
resultant octyl- and dodecyl cyclohexanes with those of the monoalkyl
cyclohexanes corresponding to them with respect to the molecular weight.
The physical constants of 1,4-dialkyl cyclohexanes (with normal radicals)
approximately agree with those of the monoalkyl cyclohexanes corresponding
to them as to molecular weight. Diagram 1 shows the direct proportional
ratio between the melting point, D 420, nD20, and the number of carbon
atoms in the alkyl radical of lt4-dialkyl cyclohexanes. The mean exaltation
value of the molecular refraction (A MR-) is +0.10. The viscosity values
D
are given in Table 2 (Ref. 2). Diagram 2 gives the logarithm of the
viscosity as a function of temperature. Diagram 3 illustrates the
dependence of the logarithm of viscosity of 1P4-dialkyl cyclohexanes on
the number of carbon atoms in the alkyl radical, Diagram 4 shows the
dependence of the molar extinction coeffioient E of the 2925 owl band
in their molecules on the number of CH2 groups. The infrared spectra
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86498
Physical Properties of 1,4-Dialkyl S/079/60/030/011/003/026
Cyclohexanes B001/Bo66
of all compounds show intense,bands at 1375 and 1450 ci- 1 corresponding to
the deformation vibrations of the CH 3 and CH2groups. In the spectrum of
diisoamyl oyclohexane, the 1375 cm-1 band is split into two bands
(1350 and 1385 am-1)v which is indicative of branching. There are 5 fig-
ures, 3 tables, and 10 referencess 3 Soviety 2 US, 1 German, 5 Britishp
and I French.
ASSOCIATION: Institut organicheekoy khimii Akademii nauk SSSR
(InBtitute of Organic Chemistry of the Academy of Sciences
USSR)
SUBMITTED: January 2, 1960
Card 3/3

SHUYKW~ N.I.; LEBEDEV, B.L.; POZDNYAK, N.A.; LUBUZHI Ye.D.
.zz-
Catalytic alkylation of tetralin in the presence of metallic aluminum.
Neftekhimiia 1 M.1:39-45 Ja-F 161. (MIRA 15:2)
1. Institut organicheskoy khimii AN SSSR imeni Zelinskogo.
(Naphthalene) (Alkylation)

SHUYKIN, N.I.; POZDNYAK, N.A.; LUBUZH, Ye,,D-
Catalytic alkylation of tetralin. Report 5: Alkylation of tetralin
with primary alcohols of Composition C7 and higher. Izv.AN SWR,
Otdokhim,nauk no.6:1098-1102 Te 161. (MMA 14:6)
1. Institut organicheskoy kbimil im. N.D.Zelinskogo AN SSSR..
(Naphthalene) (Alkylation)

FREYDLINAI.R.Kh.; YEGOROV),,Yu.P.; GMOVSKAYA, Ye.TS.; TSAO I CTS'ao I];
-- LIJBUZH, Ye.D.
Rearrangement occurring in the process of the thermal telomeri-
zation of ethylene with silicon hydrides. Izv. AN SSSR. Otd.
khim.nauk no.7:1-256-1261 J1 161. (MIRA 14:7)
1. Institut elementoorganicheskikh soyedineniy AN SSSR.
(Ethylene) (Silicon hydridea) (Polymerization)

S/02oJ61/136/002/016/034
B016/Bo6o
AUTHORSt Yegorov, Yu. P. and Lubuzh, Ye. D.
TITLEs Application of Infrared Spectra in the Region of CH Stretch-
ing Vibrations to the Determination of the Structure of
Alkanes, Aromatic Hydrocarbons, and Compounds Containing
Heteroatome
PERIODICALt Doklady Akademii nauk SSSR, 1961, Vol. 136, No. 2,
pp. 342-345
TEXTs The authors wanted to determine the range of application of infra-
red spectra in the region of CH stretching vibrations. They examined
various considerably ramified alkanes, mono- and diphenyl alkanes, some
alkyl tetralins, alkyl naphthalenes, alcohols of a normal structure,
n-alkyl bromides, ketones, and silicon hydrocarbons synthesized at their
Institute (Refs. 12-17)- Prom all these substances they prepared solutions
in CCI 4 0 - 3 g1l), and the respective spectra were taken in the
2800-3060 am-' region by an ~jVt.-12 (IKS-12) spectrometer with a UP
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Application of Infrared Spectra in the Region S10201611136100210181034
of CH Stretching Vibrations to the Determination B016/Bo6o
of the Structure of Alkanes, Aromatic Hydrocarbons, and Compounds Con-
taining Beteroatoms
prism, Table 1 gives the charaoteriatios relative to the bands of the
antisymmetric CH vibrations in the OR 2 and CH3 groups. It was noted from
Table I that the half-widths (491/2) of 2930 and 2960 cm7I bands are
only little changed in the types of compounds investigated. As there is
a linear relationship between the intensity at the band maximum and the
number of OR 2 and OR3 groups, the integral intensity of the band was
thought to represent a linear function of the number of groups. It was
established furthermore that methyl-substituted alkanes (2-methyl-,
3,5-dimethyl, 2,4,6-trimethyl alkanes, and others) differ only little
from n-alkanes as to the intensity of infrared bands. "T-shaped" alkanee
(e.g., 4-ProPyl heptane and 5-butyl nonane) on the other hand, have a
coefficient A - 100 (A denoting the effect of groups X (X - C6H 5' OR, R3Si,
Hal and others)upon the adjoining methylene groups of the aliphatic R
chain). In this manner, 1-33 of the C92 group per ramification are "lost"
for the intensity of the spectrum. When determining the structure of
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Application of Infrared.Spectra in the Region of B/020/61/136/002/016/034
CH Stretching Vibrations to the Determination B016/BO60
of the Structure of Alkanes, Aromatic Hydrocarbons, and Compounds Con-
taining Heteroatoms
compounds containing several radicals on the aromatic ring,-but only in
para and meta position, one must take account of the effect of the ring
upon each of these radicals. Results indi&ated the Buitability of infra-
re s
d spectroscopy for the determination of structure of hydrocarbon' with
a long aliphatic chain. The value of,A.is qualitatively connected with
the electronegativity of the X groups. Thus, the series
Cl >, Br > H3C-0- > OH > C< C I OH7> R3Si > C6H ~ > 'H3 >C01 1 shows how
0
the coefficient decreases. R Si is, however, more strongly electro-
3
negative than phenyl. There are 1 figure, I table, and 24 references;
10 Soviett 9 UBp 1 Canadian, and 4 British.
ASSOCIATION: Institut drganicheskoy khimii im. N. D. Zelinskogo Akademii
nauk SSSR (Institute of Organic Chemistry imeni N. D.
Zelinskiy, Academy of Sclences USSR)
PRESENTED: July 20, 1960, by A. N. Nesmeyanov, Academician
SUBMITTED: July 12, 1960
Card 3/4

AUTHORS:
TITLE:
PERIODICAL:
240.51
S/02o/61/138/004/011/023
B103/B203
Vdovin, V. M., Sultanov, R., ~ubuzh, Ye. D., and Petrov, A. D.,
Corresponding Member AS USSR
Organosilicon compounds with hydrocarbon bridges between the
silicon atoms. Alkylation-of w-cyano-alkyl trimethyl silanes
by means of halogen methyl trimethyl ailanes
Akademiya nauk SSSR. Doklady, v. 138, no. 4, 1961, 831-834
TEXT: The authors studied the production of bridge disilanes
(CH 3Y.3 Si_R _Si(CH 3)3 containing a cyano group in the hydrocarbon radical. R.
Such diailanes may be used for producing various polymers. These compounds
have so far been obtained with difficulty, The authors point out that the
cyano group bound to the P-carbon atom (with respect to Si) can be trans-
formed into various functional groups without separating the cyano-alkyl
radical from the Si atoms The reaction was conducted according to the
scheme (CH ) Si (CH ) CH CH Na , L(CH ) Si(CH ) CH(Na)CN1
3 3 2 n 2 ether 3 3 2 n
Card 1/5

40
S/6'2' 61/138/004/011/023
Organosilicon compounds with hydrQcarbon,,.. BlORB203
XCH2Si(CH 3)3 P a
(CH 3)3 Si(CH 2)n CHCH2Si (CH 3)3 +NaX, (1) under the conditions
I
CN
c' alkylation of acetonitrile, where n Is 1 or 2, and X is Cl, Br, or I.
r~fte structure of the compounds obtained was studied by their infrared
spectra. The frequency 2238 am- 1 of disilane nitriles lies in a region
characteristic of the cyano group, but is a Iiiiie lower than its value in
4.v-nitriles (CH 3)3 Si(CH 2)n CN (for n -2 and 3, 2249'em-1). This may well be
reconciled with the reduction of the frequency of an electronegative group
with increasing branching of the radical bound to this group. Besides, the
structure of the compounds produced was confirmed by their transformation
into ketones. The highest nitrile yield was obtained according to reaction
(1) for (CH 3)3S'CH2, (about 40 ~6). In the case of (CH3)3 SiCH2 C1, the
disilane nitrile yield was lowest (about 20 %). In parallel to reaction
(1), numerous by-products were formed which corresponded to the dimer of
the initial 0-cyano-ethyl trimethyl silane. The dimerization of silicon-
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2L.Oc-i
S/020 61/138/004/011/023
Organosilicon compounds with hydrocarbon... B,03/~203
free nitriles under the action of sodium is known, and was confirmed by an
additional experiment. From the two structures a8cribed to such dimers,
(A) and (B):
RCH 2 -C-CH-R RCH 2 -C-C -- R
~ I I I
(A) NH C N (B) NH2CN
the authors choose (B) on the basis ofIspectral data, where R--CH2Si(CH 3)3'
Here, they find the frequency 2201 cm- (apparatus W-12, IKS-12) which
they consider to be that of the valency group - ONN. This frequency is
reduced, apparently owing to a chain of conjugate groups. The frequencies'
3400 and 3448 am-I correspond to the symmetr.'Ao and asymmetric stretching
vibrations of the NH2 group. In the infrared spectrum of the solution of
this substance in CCI 49 the frequency 1630 am -1 is characteristic of the
- G - C b o nd .The ultraviolet spectrum of this substance i;howed an intensive
frequency 248 mA (E -46500). In the alkylation of the &L-nitrile of the
type NC -CH - CH - 0 - (CH ) S1 - (CHO a different reaction occurred:
2 2 2 3 3'
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2 W51
S/020/J/138/004/011/023
Organosilicon compounds with hydrocarbon..,, B103/B203
y-hydroxy-propyl-trimethyl silane and an acrylonitrile polymer sere formed.
In a control test (without XCH 2Si(CH 3)3 ). a y-alcohol wa8 aisu formed
according to scheme (4) (a =ether, b -polymer). Decomposition of the
systems -Y-C-C-C-M(Y - electronegative, M - electropositive atom) was
thoroughly studied by A. N. Nesmeyanov and co-workers (Ref. 14: Izbr. tr.
(Selected papers), Izd. AN SSSR, 1959~ P. 549, 678, 684), and is a
characteristic of these systems if M is a metal. In a special experiment,
'the authors found that the alcoholate (CH ) Si(CHj = ONa formed in the
3 3 2 3
reaction did not react with XCH2Si(CH3) under given conditions. There are
1 table and 18 references: 10 Soviet-bloc and 8 non-Soviet-bloc. The
three references to English-language publications read as follows: Ref. 8:
S. Nozakura, S. Konotsune, Bull. Chem. S6c., Japan, 29, No. 3, 322 (1956);
ibid., 29, No. 3, 326,0956); Ref. 10- R. A., Show, J. Chem. Soo., 1956,
2779; Ref. 11: H. Adkins, J. Whitman, J. Am. Chem. Soo., 64, 150 (1942).
ASSOCIATION: Institut organicheskoy khimii im. N. D. Zelinskogo Akademii
nauk SSSR (Institute of Organic Chemistry imeni N. D. Zelinskiy
of the Academy of Sciences USSR)
Card 4/5

C8ERNYSHEVj Ye.A.; BUGERENKO, Ye.F.; LUBUZH, Ye.D.; PETROV, A.D.
I
Synthesis of X -organosilyl of propylphosphinyl chloride and
of ethyl eater of propylphosphinic acid. Izv.AN SSSR.Otd.khim.-
nauk no.6-.1001-1005 162. (MIRA 15:8)
1. Institut organicoaskoy khimii im. N.D.Zelinskogo AN SSSR.
(Silicon organic compounds) (Phosphinic acid)

CHELfTSOVAI M.A,,; U-TSZUK-YUY [Wu-TSung-yd]i_LUBUZH, Ye.D.
Syntbesis and properties of cZ.,c,(~bi-,(p-benzy,3.biphonyl).
Izv.AN &9SR.Otd,khimonauk no.8:1.470--1473 Ag 162. OIRA 15:8)
I* Institut organicheakoy khimii im. N.D.Zelinskogo AN SSSR.
(Biphenyl)

PETROVO A. D.; KAPLAN, Ye. P.; KaAKOVA, Z. I.; ~UBI~Zqj_Ye. D.
Synthesis of o-allql and o-ax7l biphenyls. Izv. AN SSSR. Otd.
khim. nauk no.1;161-166 163. (MIRA 16:1)
1. Institut organicheskoy khimii im. N. D. Zelinskogo AN SSSR.
(Biphenyl)

L n226-63
71
ACCLSSION AITR; AP3000123 S10062163100010051082210831
AUMOR; Xegorov, ~Yu. P.; I-Vshchevua, K. S Lubuzh, Ye. 1D.; Vdovin, V. M.;
PetrovP -,A. D,
TITLE: ~rganosilicon compounds with hydrocarbon bridges between the silicon atoms
SOURM: AN SSSR. Izvestiya otdeleniye khimicheskikh nauk, no. 6, 1963, 822-831
TOPIC TAGS: organosilicon compounds, polycondensation, polymerization, polymer,
A
structure,, IR spectroscopy, aluminum. chloride, alurninum bromide
ABSTRACT: Thq, feasibility of oyathesizing polymers having alternating p-xylylene
or p-pheny ene,'radicals and silicon. atoms in the backbone by the polyco-nTensation
of 1,4-bis(trimethylsilyl)yylylene or 1,4-bis(trimethylsil~3)phenylene in the
presence of an A 11 or AI,2Br6 catalyst haa been established. OThe structure
2C"6
of 04,
previously prep=ed products of the catalyt "ati
-various a,t4--bis(trimethy.',silyl)aLt-.ane;3 as well as of the thermal pS~~ri~zatiop
of 1,1-dimethylailacyclopropane and 1,1-dimethy1nilacyclobutane have been studicl
by M spectroscopy. The structure of the polymer of 1,,I-climethylsilacyclopentane,
Card

.11
CHEL ITSOVA , M.A. ;PETROV, A.D.; LIJP'U'Zll, Yo.D.; YERIM-MWA, T.I.
Syr
, nthesis and scle(.tlve hydroVenation of tri- and pentaphemyl-
alkaines. Izv. AN SSSR Ser. kbim. no,1:124-133 165.
(m,IRA 18:2)
1. Instltut orranicheskay khImii iin. N.V. Zglinskogo AN SSSTI.

CHERNYSfEV, Ye.A.; DOLGAYA, M.Ya.-, LUBUa, Ye.D.
Addition of arylfluorosilicon hydrides to styrene. Izv. AN SSSR,
Ser. kh1m. no.43650-654 165. (MIRA 18:5)
1. Institut organicheskoy khimii im. N.D.Zol-inskogo AN SSSR.

LUBYAGIN, I.
Help to improve !he accounting on collective farms. Den. i kred.
19 no.7:69-71 r61. 1 1 (MIRA 14:7)
1. Upravlyayushchiy,Slobodakim otdelexii-yem Gosbanka Kirovskoy
oblasti.
(Slobodskoy District-Collective farms--Accounting)
(Banks-&nd Mnking)

15-57-10-14643
Translation from: Referativnyy zln=al, Geologiya, 1957, Nr 10, P 213
(USSR)
ADMOR:
Basic Equations of Ground Water Drainage in Heterogeneous Soils
(Osnovnyye uravneniya dvizheniya gruntovykh Yod k drenam v
neodnorodnykh gruntakh)
PERIODICAL: Tr. Aralo-Kaspiyak. kampleksnoy ekspeditaii AN SSSR, 1956,
Nr 7, PP 197-221
ABSTRAM: When ground waters are draining In strata of varying Wrmeability,
the strongest movement occurs in the stratum of highest permeab.lity.
Pressure difference causes ground water to drop from layers of low
permeability to layers of high permeability. The great range# of
permeability in various a4qifers allows only vertical seepage from
strata of low permeability into a layer of high permeability, and
only horizontal seepage into a layer of high permeability. Examina-
tion of a region where a layer of high permeability lies
Card 1/2

15-57-10-14643
Basic Equations of Ground Water Drainage (Cont.)
between two layers of low permeability makes it possible to
establish the following equation of flow balance:
!Yx = (wl + w2),
where Q is the inflow to a separated element of flow from a
stratum of high permeability; w 1 and w are the vertical com-
ponents of speed of movement in adjoin?ng strata. There is
also Darcy's law:
ak 92
dx
where a is the thickness of the aquifer of high permeability,
and k Is the seepage coefficient of this horizon. These
equafions form a system of cumulative differential equations.
Numerous problems are solved. Equations for a sloping level
are given and problems are broken down Jnto their component
L
parts,'for which relatively simple solutions are offered.
Card 2/2 A. F. Vollfson

L 54F17-65 FBDIEWr M/Ewo (v)/EEc (t)/EEc-4 Fo-h/Pe-5/fte-2/Pi-4 GW/WS-4
ACCMION IMI AP5014498
UP/0141/65/ooe/002/0219/0228
AU7710M MmR0k%Pj_G Aq 9Ls1jg*m F..0,1 Krot1k0Y,_Y*_L I FAU __Y, A,--I. Iif
,_M.l Gtrezhngnj#
nov, V. ]L4 P2orKfir~yeyj ljqhkVjj
-)(; Tkoits-
Fedoneyev, L. I.; V. I1!pz!qkiLiaj_Z. P.
!TI=s Observation of the radio ecliyas of tbe moon at millimeter wavelengths
AGURGEt M. Radiofizika, Y. 8, no. 2, 1965, 219-228
TOPIC TAM radioastrononW, lunar eclipse, brightness texperature, lunar surface
!material
ABSTRAM The radio emission from the moon was measured during the eclipses of 7
IJU4 and 30 December 1963, by a procedure in which toe antenna was - tpibri6di thj:ly,
gomparea, with a standard signal which consisted of the. difference
between the- emission of a section of the sky of fixed altitude and a mountiin'
slope having a tempemture close to that of the surrounding air. The work van done;
at Mt.-Aragats in Armenia (3250 m)' on T *July..jand in UsurtWs (Prikmorbkiy kr4
on 30 December. Beyeral- refinements were intr6Mwed to correct for tkie'taffitidir-
of the height of the moon 4uring the time of the eclipse. The max1pone relative
drop of effective tesWerattire was 17%. 6 A 2%, 5 2%, and 3 1 2% at wave- 7- 'i
Card 2/2

L 54817-65
Acassiox NRs Ar5o14498
lengths 1.2, 2.1, 4-0, 7-5, and 16 mm'In the eclipse of 7 My and 22.5 t 2.%,
12 1 2%, and 6 1 2% at wavelengths 1,2. 4,0, and 6.o = In the eclipse of 30 Decem-~
her. The beat Weement between the cbseryation data and the theoretically pre-
dicted cmwse of the radio br4ftw=.tqTx4ure drit ffie aclipop, for a homogly?us model
-
'
(k-tber,-~
of the moon, is obtained if T/b - (6 1 1.5 and 1.0) x 107. T - (kD*)
mal. conductivity, p--density, a--specific heat, b--tangent of dielectric loss angle
of the lunar material). This value of -r1b agrees vita previously obtained value 1
measured by a different method. "We thank the birector of the Institute of Pb7sic
Armenian AcaftT of Ociencesp At 1. Al~kharWm for the opportunity of performing
the work on the high-nountain base of the Institute wid for help." Orig. art. hais
2 figures and 1 table. [021
ABSOCIATIM radofizicheakly Inditut pri 00 rlkwskm
vinivermitate (ftdioybrales Balentifta Research Maxtitate at the GoOkly ftiver
1 00 MCLI 00 MM COM AA, N

P" "Ti 006 OW I Ook ATD PRM81 4029

I Card 94,

KAHENSKAYA, S.A.; KISLYAKOV, A.G.; KROTIKOV, V.D.; NAW/,OV, A.I.; NIKONOV,
V.N.; PROFIRIYEV, V.A.; PLECHKOV, V.M.; STREZHNEVA, K.M.;
TROITSKIY, V.S.; FEDOSEYEV, L.I.; LUBYAKO, L.V,.; SOROKINA, E.P.
Microwave observation of lunar radio eclipes. Izv. vys.
ucheb. zav.; radiofiz. 8 no.2;219-228 165. (MIRA 18-.6)
1. Nauchno-issledovatellskiy radiofizicheskiy institut pri
Gortkovskom universitete.

LUEtAIETaly, S. L., Lecturer
Ullianov Agricultural Institute
"For the realization of the principle of deva3tation.11
S3: Veterinarila 26 (3), 1949 p. 35
* 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 9 0 0 0 * * 0 9 0 *

LUBIAII,MSKTI, S. A., Cand. of Vet. Sciences
Ully-anov Agkic. Institute
~ . "Veterinary-sanitary evalvation of meat in acute fom of leptospirosis
of.calves.11
SO: Vet. 26(g), 1949) p 52
0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0.0 0 0 0 0 0 0 0 0 0 0 0

13-Y4~ N U.17'7- -'~
V,N
LUBYANETSKIY, Slivkop kfrikantov, Chevskfy arav
"DiBtinguished JubIlists, Stepan Georglyevich Dyrchonkov and Boris
Kbatlampiyevich I*dvedev"
Veterinariya, Vol 29, No 12, 1951
-rIA."fL. V - 4 ~k 41, 3 0 41 4,3

LUBYANETSKIY, S.A. Doe Agr Spi -- (qiss) "Veterinary - sanitary
-(-, x ~ -P, ~-~ 13 -0, ~~ -Cto .1
ewhada44ttm of meat product's-jtof:~~ani~jhals~--w -sarc~ospor]i-(Fi~osi - '
Ullyanovsk, 1956. 36 pp 20 cm. (Ploscow Vet Aca~AW Min of Agriculture USSR)
260 copies (KL, 10-57, 104).
li 0 _,-.
-- Iib

---- MW-LUSMWTSM~~A.---~kr--V ~ I
---- ---- --- ---- --- - ~ -
"To, the comparative appreciation of laboratorial methcds of me4t
determination in sick animals."
Veterinariya, Vol. 37, No. 5, 1960,,p. 66
.Lu 1,6, .,C ~~+ .
- IV

LUMMT-Slqyl__~ -.-(Profes-s-or -- [an-d- R-evi -1) -Abou book - "Er
ever . -~ the pert opinion
on veterinary sanitation vith fundamental technology for livestock products,
by GOREGLYAD., Eh. S. MDRYASHNOV, V. P. and SHLIPAMVO Ya. P. Veterinarno-
sanitarnaya, ekspertiza s osnovami teknologii productav zhivothovodstva. M.,
Sellkhozgiz, 1960 ...
Veterinariya, Vol. 39, no. 2, February 1962 pp* 85

LUBY,UIETSKIY, S.A., prof.
Lat us improve the veterinary hygienic training in the
institutions of higher education. Veterinariia 41
no.10:98~-99 0 *64. (KRA 18;11)
L Ullyanovskly sellskokhozyaystvennyy institute

J,TJBYANIT3FJYP G.D., Jnzh.
T~, OKB~-3195 ultrascm-L machJut. uriit for cleaning tlxead dividErs
and, ring plates. Tekst.p-rom. 2-5 nc.2i6'6--7() Ja 165.
(MIFLA 1834)
Leril-rirvadskoye TSentrallnoye kon3truktorskoye byuro po
ul't.raz-,u7kfwym i vyscjk-,chasTot-rqm ustap-ovkam.

L*9=2__,-j~6 EWA(h)/EWP(k)/ EWP.(h JD
_~WT (d)/EVIT _~WP(l)/ErIPM /E?;P(t)
-ACC.-NR: - -CODE 0 OWN 16
AUTHOR - Keller, 0. K. (Engineer)l Lubyanitskiy, G. D. (Engineer)
ORG: none
TITLE: Cleaning small.parts by means of an UZU4-01-1 ultrasonic outfit
SOURCE: Priborostroyeniye, no. 1, 1966, 16
TOPIC TAGS: ultrasonic cleaning, ultrasonic equipment UZU4-01-1 ultrasonic deaner
kBkRACTs The UZU4-01-1 ultrasonic cleaner comprises a generator and two baths. The
6r- develops
transistorized generat 10 W at 16 ' 7,5% kc and 40OV; efficiency$ 6CO.
One bath with a piezoelectric transducer is intended for ultrasonic cleaning, the
other for rinsing.-Of three organic solvents -- freon-113, gasoline B-70, and
trichloroethylene -- the first is considered preferable as it is less toxic,
explosion-safe, and quick-acting (5- 20 sec are enough for cleanina, oil-contaminated
parts). Cleaning the parts soiled with various substances (resins, rosin, flux, fate,
etc.) is briefly discussed. Orig. art. has: .1 figure and I table. [033
SUB CODE: 13 SUBM DATE: none' ATD PRESS: qi~7_3
I Card 1/1 UDC: 62-868.8

GALIPERRII , Ada Nailmovna; SKAYA, Valentina Ivanovna;
YXLI,r-,R) 02ea Konstantinovich; LUBYAII'IT~M,_Grigoriy
David.ovi h; MORIN$ L.N., red.
[Snian transistorized ult asonic unit with a 100 watt p. t;r
capacity for universal te~~hnologlcal isel Malogabaritnair.
ulttrazirukovaia ustanovka moshchnosiliv, 100 vt universallnogo
tekhnologicheskogo primeneniia na polliprovodnikovykh triodakh.
Leningrad~ 1965. 124 P. (14IRA 18:7)

I'll 14 K
S R
1,101. Kinetki of swelling rtjjjpqLrubberJn
bfa~. mixturo . of saturafid vapaurs. G,
_5TAR and 1--y- QWYANIT3911. Urhd;jyt
Zapishi D.Inruss. Univ., 1053 No. - 14, 64-71;
1051, No.,'28M; Chem. Al.,
-The -
1955, 49, 619 -~ruitallcc-xvcight method
ounined litsied ca dettrigilling- ,7G the COUTS"
awltilill.-I tile cbanezs ~Uthe ~afmzitanvc of a &on-
;dcnsk:r of whidl tho (lip.1ccuic is,the Soldied liquA
4ixture. ')'he tatio beimen thl: quantity of liquid
;taken cmd the weight -f ruljbet i-, tucll that the
~Chaljgc~i in caymcitalle'! d) jwt vs":V41 th... limits of
: tile ~rraight line Secti'll) 4 U Curve f,,r tile relation
'betwe'"I capa6muce and coulpoii'i'm of tile biliftry
mixture. Th,: swelling oi mbbur in tilt! sjfinatud
)repour-i of vlixmv~s of I-I.FlZem with ethyl nild With
butyl alcohol ii StudiA,

S106416010001006100211011
B02O/BO54
AUTHORSi LubyanitskiX, I. Ya., Miriati~ R. V., and Furman, Mi. 3,
lof Cyclohexanol and Cyclohexanone by Nitric Acid
TITLE; Oxidation
Under Pressure. Oxidation of Cyclohexanol by Nitric Acid
Under Pressure Without a Catalyst I
PERIODICAL: Khimicheskaya promyshlennost', 1960, No. 6, pp. 15-20
TEXT: The oxidation of cyclohexanol with nitric acid in the liquid phase
to adipic acid was first performed by N~ D. Zelinskiy who used ammonium
vanadate as a catalyst, SeO 21 salts of metals of variable valence, V2051
combined Cu 2+ - ammonium-metavanadate catalysts, and ammonium-vanadate -
sodium-nitrite catalysts were used later. Ye. M. Zillberman, S. I.
Suvorova, and Z. S. Smolyan (Ref. 10) studied the effect of additions of
copper, ammonium vanadate, bismuth nitrate, and of the combined Cu-V
catalyst'. Further, the authors studied the positive effect of nitrogen
oxides dissolved in nitric acid, of pressure (see the papers by
S. S. Nametkin (Ref. 17) and M. I. Konovalov (Ref. 18)), of temperature
Card 1/3

856hi
Oxidation of Cyclohexanol and Cyclohexanone S/064/60/000/006/002/011
by Nitric Acid Under Pressure, Oxidation of B020/BO54
Cyclohexanol by Nitric Acid Under Pressure
Without a Catalyst
and concentration of the nitric acid, and of the quantitative ratio
between the oxidized compound and the nitric acid. In the first step, the
reaction temperature should be as low as possible., The temperature in the
second step of oxidation has a considerable effect on the adipic acid
yield. The reaction was conducted at an ENO 3 concentration of about 60~-,
a molar ratio of ENO 3 : cyclohexanol = 6, and a temperature of 5500 in the
first step. The oxidation was performed in a 500-cm 3 stainless-steel
autoclave. The determination of adipic, glutaric, and succinic acid in the
mother liquor and the wash waters was made by means of partition chromato-
graphy on diatomite with the assistance of G. T. Levchenko and I. G.
Solov'yeva. The pressure dependence of the reaction was investigated at
pressures from 1 to 15 atm., In the pressure range 1-10 atm, the yield in
adipic acid and liberated gas is not influenced by pressure, The adipic
acid yield is slightly reduced at higher pressures. The pressure depen-
dence of the yield in lower dicarboxylic acids is complicated., a
distinct minimum occurring at 10 atm in glutaric and oxalic acid as well
Card 2/3

856hi
Oxidation of Cyclohexanol and Cycloi-exanone S/064/60/000/006/002/011
by Nitric Acid Under Pressure. Oxidation of B020/BO54
Cyclohexanol by Nitric Acid Under Pres.-!ur---
Without a Catalyst
as in CO 2' The yield in succinic acid rises linearly with pressure, The
pressure-dependence curve for the yield of the sum (110 + N02) shows the
same course as that for glutaric and oxalic acid as well as CO . On the
basis of the reaction mechanism assumed) the consumption of ni?ric acid
is calculated, and the results are compared with experimental data
(Table 4). The reaction mechanism assumed was also confirmed by the
calculated composition of the gaseous reaction products. and a number of
theoretical and experimental data. There are 3 figures, 4 tables, and
24 references: 9 Soviet.. 6 Usi 5 British, 2 German, I Canadian, and 1
Austrian.
Card 3/3

'~~AN~ITSKIY~Ija~.; HIRAM, R.V.; FURMNO H.S.
0,
Oxidation of avclohezaaol and cyal Mxanone by nitric
acid under pressure. Khims promo aoo 6:453-458 s l6o.
(MIU 13 11)
(C~clobexanol) (Cyolohexanone) (Nitric acid)

S106 60/000/007/001/010
B020XB054
AUTHORS: and Furman., M. S.
TITLE: Oxi of Cyclohexanol and Cyclohexanono by Nitric Acid
Under Pressure. Oxidation of CXclohexanol~y Nitric Acid
Under Pressure in the Presence of.a Catal t
PERIODICAL: Khimicheskaya promyshlennoW, 1960, No, 7, PP. 1 - 5
TEXT: Nearly all publications concerning the use of catalysts for the
oxidation of cycloalkanes and their derivatiV88 are written in the form
of patents. The mechanism of catalysis in this process is unclear. Ac-
cording to Ye. N. Ziltberman et al., Cu- and ammonium metavanadate ions
have different effects on the yields of lower dicarboxylic acids. While
the glutaric acid yield is reduced in the presence of Cu, the cxalic
acid yield practically vanishes in the presence of ammonium metavanadate.
These phenomena are also observed with the use of a combined catalyst;
here, the adipic acid yield considerably exceeds the total attained with
a separate use of Cu and ammonium motavanadate. The catalytic action of
vanadic anhydride and ammonium metavanadate was also observed in
Card 1/4

Oxidation of Cycl none S106 60/C)OO/007/00'/O-,O
ohexanol and Cyclchexa
by Nitric Acid Under Pressure. Oxidation of B020XB054
Cyclohexanol by Nitric Acid Under Pressure in -he
Presence of a Catalyst
idations of other cycloalkan-~-.s and aliphatl.:7 nompeunds with HNO
x~ 4, 3' All
o
publications are in agreement as to the question. of the catalyst, dosage.
In the present paper, the authors studied thesF pr-~blems by the example
of oxidation of cyclohexanol with nitric acid, as well as the mechanism
of action of the combined catalyst. 6,6--nitro.-hydroty-imino hexanoic
acid (I) was synthesized as an intermediate to investigate the inter-
mediate stages of the reactionj I was oxidized with nitric acid to
adipic acid at 60-800 C. The optimum ratio Df 3omponents was at an HNOA
concentration of 55% and a molar ratio 11NO :C H 011 the temperv!."*
3 6 11
in the first reaction stage (introduction of raw material) was 600C~ lni
in the second stage (end of oxidation) 1OOoC. The total concentration
of the catalyst was 0.01 moles/1 each, whtle thq ratio between the
catalyst components was changed within the whole concentration range.,
Fig.1 shows the results of these experiments,, The optimum molar r&tlo
CU:NH4VO 3 is 1, while other authors stated 5-5. To investigate the
Card 2/4

Oxidation of Cyclohexanol and Cyclohexanone S/064/60/000/007/001/010
by Nitric Acid Under Pressure. Oxidation of B020/BO54
Cyclohexanol by Nitric Acid Under Pressure in the
Presence of a Catalyst
stages of the process with the use of a catalysts I was synthesized at
concentrations of the combined catalyst Of 0-0-05 moles/I, and a constant
moiar ratio Cu:NH VO 3 - 1. Fig.2 shows that, the yield in I mainly depends
on the concentration of the catalyst, a concentration between 0.01 and
0.03 moles/1-being the optimum. In the oxidation of I with 67~6 HY05, at
60-800C7 I is quantitatively transformed to adipic acid (Table 1).'
The authors studied the stability of glutaric, succinic, and oxalic acid
in boiling with 43% ENO in the presence and absence of the catalyst, and
give the results in TMe 2. They investigated the effel:~t of an over-
pressure of 1-15 atmospheres on the oxidation of cyclohexanol with
60% HN03. Fig-3 shows the pressure dependene~e of the yields in dicar
boxylic acids and C02, and Table 4 gives the mean yields in gaseous
products per I mole of dicarboxylic, acids. Fig.2 shows that the effect
of the catalyst is only noticeable in the formation of 1. Optimum over-
pressure is 2-4 atm. The authors determined the reaction mechanism and
the consumption of HN03 both theoretically and practically. G.I.Kostylev
Card 3/4

Oxidation of Cyclohexanol and Cyal'ohexanone S106q601000100710011010
by Nitric Acid Under Pressure. Oxidation of B020/BO54
Cyclohexanol by Nitric Acid Under Pressure in the
Presence of a Catalyst
and Ye. I. Ishchenko assisted ir. the exper.imental part of Qc. investiga-
tion. There are 3 figures and 4 tables..
j
Card 4/4

s/o6 60/000/007/002/010
B020YB054
AUTHORS: Lubyanitskiy, I. Ya., Koetylev, G. I., and Furman, M. S.
TITLE: Oxid of CXclohexanolland Cyclohexanone by Nitric Acid
Under Pressure. Oxidation of Cyclohexanone and Its
Mixtures With Cyclohexanol by Nitric Acid Under Pressure
Without a Catalyst
PERIODICAL: Khimicheskaya promyBhlennost', 1960, No. 7, Pp. 5 - 9
TEXT: The oxidation of cyclohexanone by nitric acid has been much less
investigated than that of cyclohexanol. Cyclohexanone is oxidized with
61.3% nitric acid to adipic acid at 85-900C with a yield of 65-73% of
the theory (Ref-7). The investigation of this reaction has gained con-
siderable importance in recent years since the oxidation of cyclohexanone,
like that of cyclohexanol and similar compounds, forms the basis of the
industrial method of producing adipic acid (Ref.2). The authors studied
the effect of pressure on the course and yields of oxidation of cyclo-
hexanone by nitric acid, as well as the dependence of the yield in di-
carboxylic acids on the composition of the cyclohexanol - cyclohexanone
Card 1/3

ov
Oxidation of Cyclohexanol and Cyclohexanone 3/064/60/000/007/002/010
by Nitric Acid Under Pressure. Oxidation of B020/BO54
Cyclohexanone and Its Mixtures With Cyclohexanol
by Nitric Acid Under Pressure Without a CatalyBt
mixtures during their oxidation by nitric acid. Pure cyclohexanol and
60% HN03 were used for the experiments at a temperature of 1560C. The
oxidation of cyclohexanone without the use of pressure was conducted
at 75-6000. The authors made experiments of cyclohexanol oxidation by
nitric acid in the presence of urea nitrate. Table 5 and Fig.4 show the
effect of pressure on the yield of cyclohexanone oxidation by nitric
acid. Table 6 gives data on the yield in gaseous reduction products of
nitric acid. The authors studied the oxidation of cyclohexanol under at-
mospheric pressure and in the presence of urea, and found that under
these conditions cyclohexanol oxidation begins at 700C only (without ad-
dition of urea at room temperature), and that the adipic-acid yield
drops considerably with increasing urea nitrate concentration (Table 7).
The results of oxidation of cyclohexanol mixed with cyclohexanone are
given in Tables 8 and 9, and in Fig-5. Cyclohexanone is oxidized by
nitric acid at higher temperatures than cyclohexanol) the adipic-acid
yield being much lower than with cyclohexanol. In the first step, cyclo-
hexanol is oxidized to cyclohexanone; the end product is nitrous acid
Card 2/3

Oxidation of Cyclohexanol and Cyclohexanone S/064/60/000/007/002/010
by Nitric Acid Under Pressure. Oxidation of B02O/BO54
Cyclohexanone and Its Mixtures With Cyclohexanol
by Nitric Acid Under Pressure Without a Catalyst
which, for its part, forms adipic acid. At lower temperatures, the pos-
sibility of cyclohexanol oxidation by HN03 is determined by the presence
of mobile hydroxyl hydrogen in the cyclohexanol molecule. In cyclo.-
hexanone, the adipic-acid yield considerably depends on pressure (in
contrast to cyclohexanol). The curve for this dependence shows a maximum
at 2 atmospheres overpressure (see Fig-4); then; the yield drops with
rising pressure. The yield in glutaric acid and C02 is practically inde-
pendent of pressure, whereas that in succinic and oxalic acid is equally
pressure-dependent. The yield of the sum N2 + N20 per 1. mole of adipic
acid rises at an overpressure of 10 atmospheres; the EN03 consumption is
also relatively high at this pressure. Ketones~ mainly cyclohexanone,
are oxidized in the enol form; the oxidation of the hydroxyl hydrogen
of the enol is coupled with the decomposition of the double bond on a
free radical. R. V. Minati and L. A. Grigorlyeva assisted in the ex-
perimental part of the investigation. There are 2 figures, 5 tables, and
21 references: 5 Soviet, 6 US, 4 British, 1 French, 1 japanese, 3 German;
and 1 Austrian.
Card 3/3

LUBTANITSIlYt I.Ya.; HIRM, R.V.; MKAN, H.S.
Oxidation of cyclohexanol and cyclohexanone by nitric
acid under preseqre. Oxidation of cyclahexanal by nitric
acid in the presence of a catalyst. Xhim. prm. no- 7:529w
533 o-v 16o. WU 13:12)
(cyclohexanol) (Nitric acid)
ifi

-. LUBTANITSKIY. I.Ta.; KOSTYLEV, G.I.; FORMAN. M.S.
Oxidation of cycloboxanoae and of its mixtures with cyclohazanol
by nitric acid under pressure without a catalyst. Xhim. prom.
no. 7:533-537 O,-Y 160. (MIRA 13:12)
(cyclohexanone) (Cyclohexanol) (Nitric acid)

LUBYANITSKIY, I. Ya.
Cand Chem Sci - (diss) "Study of the reaction of oxidation of
cyclohexanol by nitric acid." Moscow, 1961. 12 pp; (Academy
of Sciences USSR, Inst of Chemical Physics); 150 copies; price
not given; (KL, 6-61 sup, 199)

...LUBYAIFITSKIY, I.Ya.-,- GRIGORIYEVA, L.A.; TURIYAN, Ya.I.
Electroreduction of 6,6-nitrohydroxyiminohexanoic acid on the
drbppizig mercury electrode. Zhur.fiz.khim. 35 no.12:2820-2821
D 161. (MIRA 14:12)
1. Lisichmskiy filial Gosudarstvennogo instituta azotnoy
promyshlennosti.
(Hexanoic acid)
(Reduction, Electrolytic)
777--'-----~-~'---I 27;

KOSTYLEV, G.I.; LUBYANITSK a
Formation of nitrophenols in the oxidation of cyclohexanol by
nitric acid. Zhur.ob.khim. 32 no./+:1355-1356 Ap 162.
(MIRA 15:4)
(Phenol) (Cyclohexanol) (Nitric acid)

GOLIDMAU, A.M.2 kand.khimicheakikh nauk; ZAYTSEV, A.I.; KOSTYIEV, G.I.;
IAWTANCHUK, L.S.; LUBYANITSKIY, I.Ya., kand.khimicheskikh na-uk;
MOBRAZIENSKIY, V.'A-. khimicheskikh nauk;
Prinimali uchasti7e: ZHADIN, B.V.; VESELtCHAKOVA, T.L.; SEDOVA, S.M.;
TRUBITIKOVA, V.I.; KUPIN, M.I.; ZHUKOVA, Ye.I. -
Preparation of adipic. acid in a continuous pilot unit.
Khim.prom. no.5.323-327 MY 162. (NIRA 15:7)
(Adipic acid)

LUBYANITSKIX, L.Yjaq) KAMIRSKAYA Ye.K.
Intermediate stages of the reaction of cyclohexanol
-caddation by nitric acid. Zhur.ob.kh" 32 no.11:3495-3502
N 162. (MIRA 15:1-1)
(Cyclohexanol) (Oxid4tion)

LUBYAIIITSKIX-j,-;-X4.*
OpMmlm temperature of the oxidation of cyclohexanol, with nitric
acid. Zhur. prikl. khim. 36 no.4:860-865 Ap 163. (WRA 16:7)
1. Lisichanskiy filial Gosudarstvannogo proyektnogo i nauchno-
issledovatel'skogo instituta azotnoy promyshlennosti.
(Cyclohexanol) (Nitric acid)

ACCESSION NRi AT4033531 8/0000/63/000/000/0017/0050
AvrHORI GoIldmans A. Me (Candidate of chemical sciences); Kosty*lev, 0. 1.;
'LubyanitakLy, IeYao (Candidate of chemical sciences); Minati, Re V.;
iy, V. A.; Sedova, So He; Trubaikove, V. I.; Furman, Me So
(Doctor of chemical sciences)
TITLE: Derivation of adipic acid by nitric acid oxidation of the products of
air oxidation of cyclohexane
SQURCE- Poluprodukty* dlya sinteza poliamidov (Intermediates for polyamide
synthe;is). Moscow, Goskhimizdat, 1963, 17-50
TOPIC TAGS: adipLc acid, cyclohexanol, cyclohexane, phenol, nitric acid, cy-
clohexane air oxidation, cyclohexanol air oxidation, cyclohexanol nitric acid
oxidation, adipic acid derivation, phenol hydrogen reduction, nitric acid
oxidation catalyst, adipic acid plant, bulk reactor
ABSTRACT: This extensive report reviews existing literature on adipic acid
and its derivation, considers In detail the theory and mechanism of cyclohexanol
oxidation with nitric acid (chemical equations ara'included) and reports the
Is
effect of various catalysts on the efficiency of the process.
Card .1/4

ACCESSION NR: AT4033531
Experimental studies of the process (equipment illustrated) were carried out at
1, 3.5 and 7 atm, lot stage temperature 70C, 2nd stage 1000, nitric acid
concentration 57% by weight, weight ratio of (10M) nitric acid to organic
raw material 4.5:1. Results are tabulated (see table I in the Enclosure).
Special experiments concerned X-oil residue and its oxidation with nitric acid.
Analysis of the derived adipic acid showed that double recrystallization (water)
and activated carbon purification of the latter provides material satisfying all
government specifications relating to production of the so-called"Aul salt
(a polycondensate of adipic acid and hexamethylenediamine). Experimental con-
tinuous production equipment capable of producing 100 kg of adipiC acid per day
was assembled and used in a series of experiments to study design requirements
and optimal process factors for industrial production. The experiments in-
--volved cyclohexanol derived from hydrogen reduction of phenol and atmospheric air
oxidation of cyclohexane. First stage temperature was 55 to 70C (60 to 65C
for phenol-derived material)l second stage and blow-off column was at 100CS
nitric acid concentration 57% by weight, weight ratio as above was 4 to 4.5:1.
It is concluded that bulk type reactors are suitable for continuous nitric acid
oxidation at atmospheric pressures Maximal yield of adLp1c acLd from phenol-
-derived cyclohexanol in the presence of a catalyst was 1o25 kg per I kg of raw
matejrial. "The method of dispersion chromatbgraphy on diatomaceous brick was
2A
Card

ACCESSION NRt AT4033531
developed by 0, To Levchenko, 1e Go BolovIyeve and I* Go Malkova of GLAP* V9 Re
Ruchinskiy of GZAP also took part in the work." Orig. art. bait: 11 tables, 6
graphs# 7 illustrations and 14 chesical formulase
-'ASSOCZATMN: None
SUBMITTED: 120ct63 DATE AGQ: 06Apr64 RML: 01
SUB CODE: 00 No REY SOV: 019 OTHER: 012

ACCESSION hR: AT4003531
XNCWSURE: 01
Table I
Oxidation of cyclohexanol at atmospheric
pressure.(catalyst in % of the weight of
organic raw material
0. 1 cu, 0. 2 W%V03)
Yield of di- Nitric acid
Composition of carboxylic consumption,
Organic raw reaction gases,. acid,'g/g g/g of odipic
material Vol. % of org anic acid
raw materials
glu- suc-
adi- taric ci-
hv~s No Pic a- acid nic
Cyclohexanol acid
from phenol
[23.
2.6.. 7143 1',; 02 007 1.*29 6.035
1004 a 0,02
from cyclaheoiane, 9,s 10 ~ 1, 11 10 j
32,03.1 -1.29 0.110 1,04
4/4

LTJBYANITSKIY, I.Ya.
Kinetics of cx.idaticn of cyclr'-~e=nona and 3-mtbylcyclo-
hexanone with ammonium metavar-adate irt acid media. Kin. i kat.
5 no.2:235-239 Mr-Ap 164. (MIRA 17:8)
1. Gosudarstvenn~7 nauchno-iseledovateliskiy i proyektsnyy
institut azotnoy pronyahlennosti i produktov organicheakogo
sinteza, Severodonetskiy fi3ial.

LUBYANITSKIY, I,Ya.; MINATI, R.V.; FURMAN, M.S. (Moscow)
Kinetics of conversion of-6,6-nitrohydroxyiminohexanoic acid to
adipic acid. Zhur. fiz. khim. 36 no.31567-574 Mr 162.
(MIRA 17:8)
1. Gosudarstvennyy institut azotnoy promyehlennosti.

GOI. L(JBYANITSKI,7. I.Ya.; -.M.; TRUBI'llf"V',
r.
FIJTI~IIANY -
ll-)rhanl on of cataly~ds -f cyolohc-xan. ' (-.Y.! da tif,n by ! - ~- - - f-.. -- :.
Zhur.prilcl.khim. 37 no.7:1563-1569 J".1 164.
~., - -L., -. ", , , "

LUBUNITSKIY,-J.Ya.; ZAYTSEV, P.M.; ZAYTSEVA, Z.V.
. - -. . ~, -.- -.1; - . - I I
Polarographic study of the aci-nitro conversion of 1',2-nitrocyclohe:mno!
and 1-nitrocyclohexene. Elektrokbimiia 1 no.8:990-992 Ag '65. (MIRA 18:9)
1. Gosudarstvennyy Inatitut azot-noy promyshlennosti, Severodonetskiy
filial*

PYATUNIN, B.V.; SANACHIN, A.V.; SULTANOV, B.Z.; LUBYANSKIY,
ABATUROV, V.G. - .......
Preliminary data on the crookedness of holes in case of boring
with hydraulic-percussion equipment. Razved. i okh. nedr 31 no.
2:48-49 F 165. (MIRA 18:3)
1. Severo-Kazakhatanakoye geologicheskoye upravleniye (for
Pyatunin). 2. TSentrallno-Kazakhstanskoye geologicheskoye
upravleniye (for Sanachin). 3. Sverdlovskiy gornyy insti-
tut (for Sultanov, Lubyanskiy, Abaturov).

LIJ BYANS KIY .-XL.-N.
Methodo for the accelerated processing of the field dqt.-- of
radiometric measurements. Geo;#. razved. no.16:101--05 164.
(MIRA 18:2)

LUWNil~-,14-10' 1nzh.
Gazli-Ural gas pipeline is a great construction of the seven-year
plan. 5troi.truboprov- 5 no.6:1-5 Je 160. (MIRA 13:7)
(Gas., liatural--Pipelines)

lUBYAITYY, I.Ya., inzh. (g.Pereyaslav-Khmel'nitsVy)
Operation of the Trubezh drainage and Irrigation system. Gidr.i
mel. 12 no.2:16-18 F 160. (MIRA 13:6)
(Trtibezh Valley-Drainage)

11UTHORS: Goncharenko, V.; Lubyanitskiy, N. SGV-107-58-8-23/53
TITLE: Radiofication of tho Crimea Oblast, (Iz opyto radiofikataii
krymskoy oblasti)
PERIODICAL: Radio, 1958, Nr 8, Pp 18-19 (U.GSR)
ABSTRACT: The receiver described is fixed-tuning circuit using a cry-
stal detector and two transistor triodes as AF amplifiers.
The set can be used as an "ether radio-point" in conditions
where a wire-broadcast network is ir-practible. The coil is
adjusted to a nearby local station and the whole set can
be assembled on a panel and inserted into a loudspeaker ca-
binet. Torch batteries in series or a section of an HT bat-
tery can be used as a power source. A two-beam L or T an-
tenna may be used. Sets of this type have been used by the
authors in the Crimea oblast), but they suffer from low se-
lectivity. Efforts are being made to produce a similar set
v.-ith better selectivity. There are two drawings and 1 cir-
cuit diagram.
1. Radio receivers--Design 2. Crystal detectors--Appl.l'cations
3. Transistors--Applications 4. Radio receivers--USSR
Card 1/1

JKORZH, A. (UB50YI) (P,-Bnllshoy Tokmak); LUBYANKO, V. (selo Uzin, Kiyevskoy
oblasti)
Surprise visit by ropresentatives of the periodical "Radio."
Radio no-7:12 J1 158. (MIRK 11:9)
1. Nachallnik radiostantaii v Bollsho-Tokmakskom rayone (for
Korzh).
(Radio clubs)

LTUBYAKOT, I., inshener (gorod Bratsk).
Im ".. I- i~
An-2 at the construction site of the
Station. Grazbd.&Y. 13 no.9:33 S '56.
(AeromLutice in agriculture)
Bratsk Hydroelectric Power
(KLRA 9-:11)

LUBYANOV, I.P.; NOROKHA, Yu.M.
Prevention of allga growth in the water reservoirs of
electric power plants. Elek. sta. 35 no.302-37 Mr 164.
(MIRA 17:6)

LUBY13%70V' 1. F.
Freash-Water Pauna - Dnieper .Peservoir
Benthonic fulinq of the Dnieper Reservoir and the problems of biologicRl propagation.
Zoc'-'.. zhur. , 31, No. 3, 1952.
9. Monthly List of Russion Accessions, Libr,)ry of Oongress, October 1952, 1311CL.

1 . "" TUllt'TEILI, P.A.,Prof.; LUBYAINOV, I.P.
"I
2. u'-;j"a (6oo)
4. Fresh-Water Fauna
7. Acclirmatizing fauna serving as fish food in reservoirs and other water bodies
of the southeastarn Ukrainel Prof. P.A. Zhuravell, I.P. Lubyanov, 4b.khoz.
29 no. 3, 1953.
9. Monthl List of Russian Accessions, Library of Congress, APRIL -1953, Uncl.

LTJBYANOV Iq?j
Formation and ways of directed change on beathouic fauna of small reser-
voirs in southeastern Ukraine. Zool.zhur. '1~12 no.6:1074-1083 H-D '53.
(MLRA 6:12)
1. Nauchno-isoledovatellskiy institut gidrobiologii Daepropetrovakogo
goeudaretvennogo universiteta.
(Ukraine--Yreah-water fanna) (7?raeh-w&,',qr fauna--Ukraine)

LUBTANOV, I.P.
Benthonic fauna of the Holochnaya River. Zool.zhur. 33 no.3.-
537-543 MY-Je 154. (MA 7:7)
1. Nauchno-issledovatellskiy institut gidrobiologii Dnepro-
petrovskogo gasudarstvennogo universiteta.
(Holochna7a river--Fresh-water fauna) (Presh-water fau-
na-Molochnaya river)

lUBIYABOV,I.P.
Wash of Dnieper River bottom fauna and the significance ofthis
phenomenon in the formation of fauna in the Middle Dnieper.
Dop. AN URSR no.2:179-183 155. (MIRA 8:11)
l.Dnipropetrovslkiy naukovo-doslidchii institut gidrobiologii.
Predstaviv diyaniy chlen Akademii nauk URSR V.G.Kaslyanenko
(Dnieper River-Fresh-water fauna

WBIYANOV,I.P. - ,
,
Characteristics of bottom fauna c1istribution in the Middle Dnieper.
Dop. AN URSR no.2:182-187 155. (MIRA 8:11)
1. Dnipropetrovslkiy naukovo-doelidehii institut gidrobiologii.
Predstaviv diysniy chlen Akademil URSR V.G.Kaelyanenko.
(Dnieper -River--Fresh-vater fauna)

WBYANPV, I,P.
New species of amphipod, gamaridae in. the middle I)nieper. Dop..
UN URSR no.4;412-414 1,56, (KLRA. 9:12)
1, Anipropetrovelkly n;(Iinatitut gidrobiologii. Predstavleuo ako4#mS,-
komAkademii nauk USSR V.G. Uslyanenkoe
(Dnieper River-Amphipoda)

LUBYUNOV, I.P. --
Distribution characteristics of benthonic fauna in the Vorskla
River (vith Inglish sumwy in insert]. Zool.zhur. 35 no.4:501-510
Ap 56. (MLRL 9-.8)
1. Sauchno-iseledoratellskiy institut gidrobiologit Daspropetrovskogo
gosudaretvannogo universitsta, imeni 300-letiya vossoyedineniya
Ukrainy a Rosaiyey.
(Torskla River-Fresh-vater fauna)

LUBYANOV, I.P.
Contribution to seasonal changes in the benthonic :Eauna of ponds in
the Ukrainipn Steppe [with English summary in insert]. Zool.zhur.35
no.12:1791-1798 D '56. (MIRA 10:1)
1. Nauchno-isoledovateliskiy institut gidrobiologii Dnepropetrovskogo
gosudaretvannogo universiteta imeni 300-leti7a vossoyedineniya Ukrainy
a Rossivey.
(Sinellnikovo District-Fresh-water fauna) (Fish ponds)

V
0
~
LUBTANOV, I.P.
currence of malarial mosquito larvae following the refilling of
the Dnepropetrovsk Reservoir. Med.parax. I parez.bol. supplement
to no.1:22 157. (KIRL 11:1)
1. Iz Mauchno-iseledovatellakogo institute gidrobiologii Dnepro-
petrovskogo universiteta.
(DxmoPNTRovsK RsuRvoift-KosquiToss)