SCIENTIFIC ABSTRACT ALIKHANOV, R. N. - ALIKHANYAN, A. I.
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S
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December 31, 1967
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SCIENCEAB
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AM legal all V.A., professor, radaktor; GONCHAROV,
p
I.A., redaktor isdatelletva
[Sub-kirmaki series of the eastern part of Apsheron Province and
its oil bearing possibilities) Podkirmakineksia evita vostochnoi
chanti Apsheronakci oblasti i as neftenoonost'. Baku. Azerbai-
dzhanskoe goo.izd-vo neft. i nauchno-takha. lit-ry, 1957. 215 p.
(MIJU 10:9)
(Apsheron Frovince-Petroleum geology)
ALIMUMOT X. IT.
h ____ - __ 01110100 __
Yormation watere vt thom-sub-Kirmaki series In the Apsheron
Archipelago. Aserb, neft, khos, 36 no,41l-4 Ap 157. (MLRA 10t6)
(KIsheron Peninsula--Oil field brines)
, ALIKHAVOV, R.N. _-- -
Prospects for explo:.-ing for oil and gas pools in the Sub-lirmaki
series. Azarb.neft.Ichoz. 36 no*7:1-4 Jl 157. (MIRL 10:10)
(Apsheroji Peninsula-Petroleum geology)
MUDZFMV, S.A.; ALIKRAITOV, 1.11.
Development of oil production in Azerbaijan offshore areas. Azerb.
neft.khoz. 36 no.lL:22-25 11 11:2)
(Azerbaijan--Oil well drilling, Submarine)
ALLUA , Anver Nazarovich,
[Development of tht petroleum and the gas industries in
Azerbaijan] Rasvitie neftianol i gazovoi promyshlennosti
Azerbaidshane sa somiletie. 1959-1965 gg. Baku, Azar-
neftneshr, 1959. 93 P. (MIRA 13:8)
(Azerbaijan-Petroleum industry)
Uzerba*ui-Gas industry)
1. ALIKELMV. Z. N.
lew problems of th~) Azerbaijan petroleum industr7. Aserb. neft.
khos. 38 no.8:1-3 Ag 159. (MIRA 13:2)
(Azarbai,lan--Petroleum induAtry)
c -ALI M.NOV. 3.11. ; KAUYM&N, V.P.
Improvement ofthe wage system in drilling departyents is an urgent
problem. Azerb.neft.khoz. 38 no.11:45-48 R 59. (HIRA 13.5)
(Oil well drilling) (wages)
ALIKHkNOV,, E.N.; KULIYEV, I.P.; SAMEDOV, F.I.
CKaractaristics and principles of the efficient development of
offshore petroleum fieldo. Sov.geol. 4 no.10.-100-107 0 161.
(MIRA IJ+: 11)
1. Gosudarstvennyy nauchno-issledovatel'sk-4y i proyektnyy institut
morakay mefti,
(Azerbaijan-Oil well drilling, Submarine)
--A-L -NEANY-1-LA. ~-Jl HU SHANOV , N.A.; AK11UNUOV, V.Yu.; AI,1'1.'AUF, M.A.; A~IZBEEOV,
Sh.A.; F.ACIROV, M.A.; VEZIROV, S.A.; VOLOBUYEl, V.R.-, ELKILOV, F.M.;
GADZHYEA', N.M.; GU SEYL D.M.; GUSEYNOV, I.A.; DtIDASHEV, h.h.;
DADASHZADE, M.A.; DALIN, M.A.; ISFENDEROV, M.A.; KAZIYFV, M.A.;
YARAYEV, A.I.; KASSITKAY, M.S.; KELIDYSH, Y.V.; KERIMOV, A.G.;
LEMBEWSHY, A.D.; MAMEW4, G.K.; MEKHTIYLV, M.R.; YdRWYEV, S.A.;
NAGIYEV, M.F.; NUERULLAYEV, N.I.; OFUDZHEV, R.1,.: lbWZWOOV, R.A.:
RUDNEV, K.N.; SADYKHOV, R.N.; SEMENOV, N.N.; TJFCFIYEV, A.V.-,
TOPCHIBASHEV, M.A.; TAIROVA, T.A.; KFALILOV, Z.I.; LFENDIYEV, G.Kh.;
snymovil, Z.Z.
IUsif Geidarovich Mamedaliev; obituary. Uokl. AN Azerb. SSR 17
no.12:1123-3.126 161. (MIRA 15:2)
(Mamedaliev, Iusif Geidarovich, 1905-1961)
ALIFHANOVP E.N. --
[Forty years of Azerbaijani industry; 1920-1960]Promyshlen-
nost' Azerb&idzha:ia za 40 let; 1920-1960 gg. Baku, Azerbaid-
zhanskoe gos. izd-vo neftianoi i nauchno-tekhn lit-ry, 1960.
133 P. iMIRA 161l)
(AzerMijan-Industries)
ALI2!09S,.-E-R.; ARUSUA1401r, N.A.; AKHUNDOV, V.Yu.2 ALIZADE, M.A.; AZIZBEKOV,
bh.A.; BAGIROV, II.A.; VEZIRCV, S.A.; VOLOBUYEV, V.R.; ITKILOV, F.M.;
GADZHIYEV, N.M.; GUBEYNOV, D.M.; GUSIYNOV, I.A.; DADASIIEV, K.K.;
DADASHZADE, M.A.; DALIN, M.A.; ISKENDEROV, M.A.; KAZIYEV, M.A.;
KARAYEV, A.I.; KA&MAY, M.S.; KELIDYSH, M.V.; KERIMOV, A.G.;
LEMDERANSKIY, A.D,; MAMEDOV, G.K.; M17HTIYEV, M.R.; MIRZOYEV, S.A.;
NAGIYEV, M.F.; NASRULLAYEV, N.I.; OGUDZHEV, A.K.; RADZHABOV, R.A.;
RUDNEV, K.N.; SPS,,'CKHOV, R.N.; SEPENOV, N.N.; TOPCHIYEV, A.V.;
TOPCHIBASHEV, M.A..; TAIROVA, T.A.; KHALILOV, Z.I.; MNDIYEV,
G.Kh.; SHUKYTIROVP., Z.Z.
IUsif Geidarovicb Mamedaliev. Azerb.khim.zhur. no.6:5-6 161.
(MIRA 15:5)
(bliunedaliev, IUsif Geidarovich, 1905-1961)
ALIKHAEOV, E.N.; MIRCHINK, red.; AMINEDOV, G.A., red.
(Oil and gas fieldD of the CasPian Sea] Neftiarye i ga-
zovye mestorazhdanUa Kaspiiskogo moria. Bakup Azerneshr,
1961, 382 p. (1-111RA 17:10)
ALIKRANOV, E.N.; ASAN-NURI, A.O.; KULIYEV, I.P.; MAMOV, B.H.;
0 S.A.; TIH)FEYEV, N.S.
Off-shore oil of i,hu M.S.R. Neft. khoze 42 no.9/10i
46-51 S-0 164. (YJRA 17:12)
ani
(m la;, -18.5)
62-Rarpov 'Wt. .11
UN -no rafractiv
tadd*
e
nil of a fluid tma be detemilned m
be tWractometer it the materLod is tmasiarred
~kplwvy to a Small pieve of O~arettv paper
lit placcd Gn.live 111isul.. 1. S. SMITH
USSR/Organic Chemistry. Theoretical and General
Questions of Organic Chemistry.
Abs Joux Ref Zhur - Mimiya, No. 8, 1957, 2661:3.
Author Kololev, A.; Shatenshteyn A.i Yuryging,
Ye., Kalinachenko, V.i aikhanov, P.
Inst
Title Isomerization of Monodeuteronaphthalenes.
Orig Pub Zh. obshch. khimiit 1956, 26, No. 6, 1666
1672.
E-1
Abstract The questio,n of the possibility of transposi,-
tion, of cC-.H i-aid S'-H in the naphthalene
molecule wE,s *`nvestigated by the method of
deuterium interchange. It is shown that if
vapors of (X-eleuterona hthalene as well of
A-dauteroraplithalene fl and 113 in a flow of
nitrogen are passing above silica gel at 4200,
Card 1/3
USSR/Organic Chemistry. Zheoretical and General FI-1
Questions of',.Organic Chemistry.
Abs Jour Ref Zhur EMmiya, No. 81 lge"t; 26613.
transposition,of D and the formation of ,i
14
'xture consisting of,approximately eqr."-
M
amount 15. of"tbeAwo isomers,will be obstrved.
Dueterium ifa4,, not., transposed in the naintithalene
molecule ail, iiAisating of I and II at 4000 for
52 hours irt ii',hsenee of silica gel. The.method
,,:Lon is based on the differs- 'nee in
of invostig'ai
speeds of rogen interchange between I or II
with liquid I.Mr. The speed constants C were
determined b6tAng on experiments of int rehange
of I and II 41th HBr at 250: C in see-, is
2 to 3 x 10'"') for I and 5 x 10-5 for IL It
is shown at the same time, that oc-methylnaph-
thalene, as well as A-methylnaphthalene (III
and-IV) are converting mutually one into th-e
Card 2/3
iUTHORS: Shatenshtern, A. I., Vedeneyev, A. V., SOV/79-26-lo-3/60
Alikhanov, P. P.
TITLE: Hydrogen React~ion of Phenol, Its Ethers and of the Aromatic
Amines With Liquid DBr (Vodorodnyy obmen fenola, yego efirov
i aroraticheskikh aminov s zhidkim DBr)
PERIODICAL: Zhurral obshchey khimii, 1958, Vol 26, Nr lo,
pp 2638 - 2644 (USSR)
ABSTRACT: Shatenshteyn a.,id his collaborators had earlier found
the rules govemiing the deutero reaction in hylrocarbonz.
dissolved in liquid DBr (Refs 1,2). In this paper the
results are gi,.,en which were obtained in the h-;drojen
reaction with liquid DBr in aromatic compound-.3 that
contain substituents with an oxygen or ritro.-en atom.
The free election pairs of oxyCen or nitrogen of t--,e
substituents are in mesomeric relation to the n-electrons
of the aromatic nuclei, which fact causes an increase
of the elect-?on density in the ortho and para-atozms
(Ref 4). The af:'iliation of the proton (deuteron)
to the electron pair of the nitrogen or oxygen atom
Card 1/3 causes its trani--ition so the quaternary or ternarj ion
Hydrogen Reaction of Phe.-iol, Its Ethers and of the S07/79-28-410-3/6o
Aromatic Amines With Liquid DBr
with simple p,)aitive charge. These characteristic
features of the compounds mentioned above are the
decisive characteristics in their deutero reaction with
acids. The hydrogen reaction on phenol and it-, ethers
(C H OCH CH
6 5 31COli'DC05 )and on oromatic amines CC6H5 N(U 3)2'
(C6H5)2 NH, (C61H5)3N ith liquid D-Br as well as with
DBr+AlBr 3 ivere investigated at 25 0. In all compounds
of the first 6-roup the ortho and para-atoms react
immediately whereas in the second group this rapid
reaction takes place only with (C6 H 5)3 N, with all
others only slowly or not at all. AlBr 3 causes the
reaction of the meta-atoms in the phenol ethers and
delays the irea-~tion in (C6H5)3 N. The different behaviour
of compounds containing oxygen and nitrogen in the
hydrogen reaction with DBr+AlBr depends on their
different rela-,Ion to the ProtoA ana on the different
Card 2/3 coordination capability of oxyten and nitroeen atoms.
Hydrogen Reaction of Phenol, Its Ethers and of the 307/79-28-10-3/60
Aromatic Amines With Liquid DBr
There are .5 tittles and 17 references, 10 of waich are Soviet.
ASSOCIATION: Fiziko-khinicheskiy institut imeni L.Ya.Karpova (Physical
Chemical InstUate imeni L.Ya.Karpov)
SUBMITTED: August 20, 1957
Card 3/3
66428
,57.2- 0 0 o c, SOV/20-128-6-33/63
AUTHORS: Alikhanov, P. P., Varshavekiyq Ya. M.
TITLE: Equilibrium Distribution of Deuterium on Hydrogen Exchange With
Liquid DeuterLus Iodide
PERIODICAL: Doklady Akade:nii nauk BSSR, 1959, Vol 128, Ur 6, pp 1214-1216
(USSR)
ABSTRACT: This paper beLongs to a serieo of investigations of the isotope
equil-.1'bria. in various s-.istems of hydrogenous compounds (Refs 1-4)-
An in,restigatLon is made of the exchange reaction between the
aroma-sic C-H '3ond and thEt deuterium-containing HJ. Benzene, which
would be well suited for this investigation because of the
equivalence o:! all H ateiao, react a too slowly so that di-
pheny:' had to be used. In the dissolution of diphenyl in liquid
hydrojen iodide the 6 H-atams in ortho- and para-poaition are
easilj exchanged while the 4 H-atoms in meta-position virtual-
ly did not retict. The deuterium concentration in HJ was deter-
mined by anal,rsig of the wa-~er obtained by decom 013itiOtl Of
HJ in the nitrogen current cver CuO at 350 - 400 The reaction
with Jiphenyl took place in sealed glass tubes at a pressure of
4 - 15 atm. Aftex equilibration had been reached, the HJ was
Card 1/2 evaporated, the diphenyl in the oxygen current was burnt, and_
66428
SOV/20-128-6-33/63
Equilibrium Distribution of' Deuterium an Hydrogen Exchange With Liquid
Deuterium Iodide
the deuterium content of the water obtained was determined. The
resulting distribution coefficient a was checked by the counter-
reaction of I-substituted diphenyl in ortho- and para-position
with HJ. The experimental data on a are compared in the table
with the values calculated by means of the formulas contained
in reference 8. The values coincide iell. As is shown in fig-
ure 1, good agreement was also obtained for the other hydrogen
halides (Refs 2-4)- In the present liper the following valugs
are given for the equilibrium coeffi!.-ient a: aoo - 4.079
a250 ' 3.47 ani a 500 a 3.13. There are 1 figure, 1 tablep and
9 Soviet referDnoes.
ASSOCIATION: Nauchno-iseledovatellskiy fizi1--khb,4cheskiy iistitut im.
L. Ya. Karpova (Scientific Research ~nstituteof Phyaioal Chemis-
try imeni L. T!i. Karpov) VK
PRESENTED: June 199 1959, by S. S. Medvedev, Academician
SUBMITTED: April 13, 1959
Card 2/2
SHATEINS-7,11TP-B. A.I~; SANUKOV, 4.P.~ ALIKIL~NOV~
Deuterium exchange method for studyIng --.he catalytic actvity
of systems consisting of hydrogen acid ind P-protic acid-2.11ke
substance. Acetic acii stannic3hloride-system. Zhur. ob.
khim. 35 noJg419-05 Mr 165. (MIRA 18g4)
1. FIzAko-khimichatkiy inatitut imeni L Ya. Karpova,
M~~Wffi'
,2mo
5 78298
. sov/-(g -.7 o-3-:5o/69
AUTHORS: Shatenshteyn, A. I., Alfl(ha-ov, P. P.
TITLE: Concerning Catalytic Actior, of Iodine In the Deuterium
Exchange in Ll~uid Hydroge~ 'Jodlde
PERIODICAL: Zhurnal obst-ichey khImil, Vol 50, Nr 3,
pp 992-999 (USSR)
ABSTRACT: Rate of deutev~luin exchan of monodeuteriotoluene (I)
and monodeuter:1,obiphenyl ~,11) with HI was studied in
the presence oil iodine ,.z'z'a catalyst. HI was synthesized
in a quartz apparatus d,-,-..,r-'Lbed previously (V. R.
Kalinachenko arid other,-, ZhFKh, 50, 1140, 1956). A
test tube contEiining a thin-walled glass ampoule
filled with the investil,;ated compound and catalyst
(iodine) was attached to the apparatus to fill it with
the HI obtained After filling with HI, the
test tube was detached from the apparatus and kept at
25 + 0.20. The glass ampoule Inside the test tube
Card 1/8 was-imploded by the fl.1 vapor., and the exch'ange
Concerning Catalytic Action of! /Iodine in
7
the Deuterium Exchange in LI(,./jId Hydrogen
Iodide
T82,98
SOV/79-30-71--52/69
reaction sta-.-ted. The reagents used were prepared by
Ye. N. Yury,rir;a. Results of the experiments are
shown in Tal,le 1. Absorption spectra of Iodine in
liquid III w_~re taken at room temperature according
to a preViC,,Lisly described method (A. I. Shatenshteyn,
Ye. A. Izri-ilevich, ZhFKh, 26, 37-7, 1952). SF-4
spectrophor.ometer and a quartz cell (0.11 cm) were
used. Spzl.;Iflc electric conductivity of liquid III
was meas~'.ed at -440 and found to be equal to
2 - 10-8 :.)hm_icm_1. The measurements were taken In a
cell wt*,-.,-. nonplatinized platinum electrodes, using an
alternu-.- current bridge constructed under the supervi-
sion of,V. Ye. Kazakevich. There was no noticeable
increa.,', in th~e conductivity of the uolution after the
addit-. .:i of iodine, m-esitylene, or hexamethylbenzene.
Cata_'-,~~Ic action of iodine is due to the polarization
of H-1 in the complex formed in the ter-
nary jstein: *romatic hydvocarbon-hydrogen iodide-
Card 2/8 iodit. ,:
Oncerl I J-1 if Cz'J-k,1y A c-1 ol, I o f* u~l 1 no i~
the Doute.--iiim Eschnnire 1.n L1(juJ,;1
A 1-1) ... itiJ..
coiwarit.,,on (it' the VaLOL' of deuterium e.,-.chancre Is
L
gli.ven in TaIde 2 . The authors express thelv rratitilde
to Ye. 14. Yurygina for the ~euteri=i-contalnlniL-
- hytlro-
carborl.,; .Thel~O ~11-0 2 INIVUI-e!,; -'*) tUNOS; and 115 refer-
elle-es, j.,w U.S., Y U.K., I Germall, .94 Soviet. The 5
moBt recent U.S. and U.K. references nve: G. 01,th,
S. Kuhn., A. Puvlath, Nat :uro, )'(8, L. L.
mackol" F. SmIt, 1. Ti-cins
11 J . I V,111 deV
Farad. So', 5~, *009 ( 1957 ); V . Gold, D. P . gatchell,
J. Chem. 3oc, ., 1927, 39011, 5910 ( lQ5,c'); 11 - 1i - HYman,
M. Kilp;at-Ick, J. J. Katz, J. Am. Chem. Soc., 79, 3668
(1957); W. G. Schneider, "HydroL~en Bondiri,,-,," ed.
Had,,,J, Po';,.gamon Pre'so. N. Y., I-A (-lc,,
59
I.J.30CIATION: L. Ya. Kai,-pov Scientific Research Iwstitute of Phy.;1-
cal chemlotl'y Cj:,J.J~o-
khimlehe.nkiy In.,.itltut imen-1. L. Ya. Karpova)
SUBMITTED: April 10, 1959 Cavd ~/~9
Table 1. ReSult's Of exper-imetits on
li(iUid III.
1.4 0.80
1.4 1080
, 4
:1 1.7 04
5 4.0
1.7 4.0
NO
1.9 9.2 7. 7 itio
1.8 12 G.l
8 A.!. 5,50 24 51
1.7 5.50 2.70 /13 7.3 29
10 1.!l 5.1;fi 3.23 3 8.0 28
t 1 1.8 10 5.co :Z.02 9. 1 is
12 2.1-1 :!.! 1 11 1 o.8 18
Card JV8 Mable 1 cont'd on Card 518)
- -- - -------------
.5. ~1 1 2.! 1; i 3.6 VA)
r rt, )! I
:
,( :w ?.! I
,
;
2 2: 1 7.1 2.7
17 1 .!1 .11A 1
- 2.4.3 Z-1 12 :1. 1 41)
.
M4 % I
1
1!) 1
.7 43 14
20 1.8 14 5.5f 1 3 GI /J. .1, 13
21 1.8 5 1-1. ? I I W) 6A 7
k
2-1 0 - b.10 4.2-
23 (1.8 8.1(1 .3.97 0,8 79
24
2
6
0. 7
2A
8.10 "t
-1.
1!,
7.2
32
25 0.86 3.8 S. 1 4.93 '25 1;.Ii "I
21; 0.71 t 8.to fi.08 I F, ill 7.1,
V 071
, ~.H 7.81) 4.76 /15 15 2.0 313
is 81)
0 3.4 7.80 ~1.19 2:1 51; 1.7 24
29 0.75 5.1-1 7.80 4.27 2Y) 7~9 1.5 14
30 Lt 7.8 7.8o 4.76 12 1 1.8 14
M 0. 2 11 7.80 S. I G 20 1.8 2
32 0.83 12 7.80 5 2:1 j.!1 7
33 (11,82 S7 7.80 4 36 2.1 5
Card 5/8 (Key to Table 1 o1i Card 6/8)
Cbneerning Catalytic Action of Iodine in 78298
the Deuterium Exchange In :L'Aquid Hydrogen SOV/19-30-3-52/69
Iodide
Key: (a', C 102 is the number (.-)f hydrocarbon
I A rD
moles Per IT.Ole Of HI; (b) C, is the iodine concen-
v2 0
tration In moles per mole ot' 111; c) CB Is the deu-
terium concentration in water after the precipitation
of the compound bel'ove, the experiment (in atom %);
(d) C-Bf E,ft~r the end or the experiment; (0) T Is
duratton of the experiment it) hours; (f) I-, is constant
of the rate of deuterium exchange; W k 1~/'c J2 Is
the specific rate constant in reference to the. con-
centration of iodine In the solution; (11) C = C ArD/
/CJ2; (i) p-D-toluene; (J) o-D-toluene; (k) p,-D-bi-
phenyl; ('I) o-D-biphenyl.
Card 6/8
Act 1 On 01' TudDo.- in
the J~outovlunl
Iod ide
Fig. :1 . AWiouption spect-,,~~
of iodine noluttom"';
ill cclj~; (2) in C-11,; 2
6 0
Jn liquid III
Lj
itI
J610 4D9 500 Mo
Card 7/8
C,oncevning %Catalytio Aotlot) ol' IoAlne 1i;
the Deuterium J-1'x(.-hanp-,e in Liquid Hydroi,en, ,O,.l
Iodide
Table 2. Comparinon of the constaiit:, of deute-vitun
0
exchange rate with dl.fferent hydrogen halides at 25
(see
IW2
Key: (a) Hydrocail)ovi; (b) o-D-toluene; (c) p-l-toluene;
(d) o-D-biph2nyl; (e) p-D-biphenyl; (f) a -D- naph-
tha-lene.
c ar d 8 /8
AUTHORS: Yurygina, Ye. N., AM-hanov, P. Pop s/076Y60/034/03/015/030
Izrailevich,___.Ye! K. - B115/BO16
Shatenshteynp A .1.* Moscow)
TITLE: The Kinetics of Deuterium Exchange of the Isomers of Monodeutera-
tolueneA monodeut,oro-diphenylAand Monodoutero-naphthalone With
Liquid Hydrogen Bromide and a Solution of Potassium Amide in
Liquid Ammonia
PERIODICAL: Zhurnal fizicheak-)y khimii, 1960, Vol 34, Nr 3, PP 587 - 593
(USSR)
TEXT: The aim of the investigation under review was the determination of the
factors of the partial rate f i-a the hydrogen isotopic exchange of the sub-
stances mentioned in the title with the reagents likewise mentioned in the
title. The synthesis of monodeuterated bydrocarboneg the deuterium conoentra-
tion in water on combustion of the hydrooarbonal %nd the carrying out of ex-
periments are aesoribed. The rale constant of the deuterium exchange is cal-
culated by an equationand, when using ammoniacal solutions, by a simplified
form of this equation. The resulAs of the measurements made with liquid HBr
are given in table 1, those of Zbe experiments with ammoniacal solutions in
table 2, and the mean values of the constants of the deuterium exchange rate
Card 1/3
The Kinetics of Deuterium Exchange of the Isomers of S/076/60/034/03/015/038
Monodeutero-toluene, Xonodeutex-o-diphenyl, and Xono- B115/Bo16
deutero-naphthalene With Liquid. Hydrogen Bromide and a
Solution of Potassium Amide in Liquid Ammonia
in table 3. The activation energy of deuterium exchange is also given. Table 4
presents the factors of the partial rate f of the deuterium exchange of iso-
meric monodeuterated hydrocarbons with a KRH 2 solution in NH 31 and with HBr.
The order Df the partial rate Vaotors in the isotopic exchange between non-
equivalent deuterium atoms in Ahe toluene and diphenyl molecule differs in re-
actions with acids and with lyez, which is due to the different mechanism of
these reactions in which the ocnjugative and the inductive effect considerably i0
manifest themselves in the mutual action of the atoms in the hydrocarbon mole-
cule. The rules in the deuterium exchange in toluene and diphenyl indicate that
the inductive effect of the methyl group has the reverse sign compaxed to that
of the phenyl group. Pinallyl It can be said that the acid and the, base react
in the deuterium exchange with the carbon atoza of the CH-bonds and the base
with the hydrogen atoms of the CH-bondef and protonize those atoms. A method
is described for obtaining isomeric monodoutero-diphenyle. It is described
exactly how the authors divided this work among themselves. There are 4 tables
and 19 referenaeal 12 of which are Soviets
Card 2/3
The Kinetics of Deuterium Exabange of the Isomers of 8/076/60/034/03/015/038
Yonodeutero-toluene, Monodeutero-diphenyl, and Mono- B115/BO16
deutero-naphthalene With Liquid 1~ydrogen Bromide and a
Solution of Potaasium, Amide in Liquid Ammonia V-1
ASSOCIATION: Fiziko-khimiohealciy institut im. L. Ya. Karpova (In!Ltitute of
Physical Chemist::Z imeni L.- Ya. Karpo )
SUBMITTED: June 13, 1958
Card 3/3
ALIKHANOV, 1'. P.
Cand Chem Sci - (diss) "Investi~-_ation of reactions of deutero-
exchange of some aromatic compounds with liquid hydrogen halides.
Moscow, 1961. 15 Pp; (Ministry of Pilrber and Secondi3ry Special-
ist Education KFII"R, Moscow Order of Lenin Che;Actal-TechnoloFica).
Inst imeni 1). 1. Mendeleyev); 150 coules; price not r.Aven; (KL,
5-61 sun,, 175)
SHATENSME11, A.I., prof.; 7YRSK1Y, Yu.11., kand. khili,i. nauk.;
PHAVIKOVA, N.A., kwad. t.ekhri. nauk; A.~.jKHAVOV,11.P.P
kand. khim. na",; VDANOVA, K. I., kand. kUm. nauk;
IZYM211KOV) A.Les m~lad. narchn. sot.r.; LEVINSKIY, Yu.V.p
red.
[Fractical .-laboratory manual on the determination cf the
molecular weights and molecular we.-Lght distrilnition of
polymers] Prakticheskoe rukovodAvo po opredolenliu wo-
lokuliarnykh. vescv i rwJ.ekulJa-rno-vewvo,gO raupreklale-
niia polimerov. [By] A.I.Shatenslitein i dr. Vosk-va,
Khimiia, .1964. 1.62, p. (1,1111A IS: 2)
M
USSR/Physics Heat of evaporation cf 02 FD-3283
ca~A zi/i Pub. 146"- 42/44
Author : Alikhanov, R. A.
Title : Heat of evaporation 3f oxygen in the interval of temperatures 8o-io6OK
Periodical : Zhur. eksp. i teor. tiz., L>q, no 6(1-2)., Dec 1955, 902-903
Abstract : The author made 35 mil-w3urements of the heat of evaporation of 02 for
7 different temperatAxros, obtaining values different from thoze of
other researchers; e.g.. he obtained L (cal/mole) z 1628.ril.3 at TOX
90.19. He gives the other values of L for 6 other temperatures and
the empirical expresoion relating L to T; e.g.
e - 67208.68(T(j,.-T) - 555-221(Tcr-T)2 + 2-32505(Tcr-T)3.
The author thanks P. G, Strelkov for his attention and interest. Five
references.
Institution: Institute of Physical Ivoblems, Academy of Sciences USSR
Submitted : July 21, 1955
V 4T -
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Of ~'~llt"'erroP`9110t'r"' L"C03, F`C03 alld. ""P-11,
phic study
cz~.
o s 1 1,9 5 9 .10 pp (Acrid Sri IMR. Ilirt of Y-hysicA Problenn.0.
110 copies. j Bibliogr:lphy L-A und Of text (10 ti'Lllc.--)
(IM, 39-59olOO)
24(c)
'amt.
1. X.. Doctor of kh.T.L..l and Kath.-tic.1 3.1-0-.
21TIA. 01 1" ". 'r.t.r. 'Aysics (Inslodow"Iya po
ft.. alk.
VILRIODICAL, Tm-Mik Ak&dmll Sauk 3332, 1959. Er 2. vp 98-100 (033a)
The -th ~a U.5 PrQtlar. L"a P1444 Is
TbIllst true October 27 to No,weabor 1, 195a. It was att*nd*4 by
OWN1.1 frame 114.60. Kb&r-k v. L.-I-exad, T%tIA-
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Averdlo ad Imyr,. by
4 p
&I aa ... d, -porAiquidity of liquid hall= 11.
=
forroma.gust.-ma, m,CmoM-r.-L.tj,s front. Th. following
"part. and o- heard, L. A. Abrjj2ko, k. F.
_Eq~ r.po' M& on the Investigation of the propertle! or
"ProC-44-0tiew, alloys.. A. A. A~,rlko-, L. P. Gor- to, -1- X.
" of properties of S.Pracooductors In "a hteo-
~MLk*v
%#Ay was tIo field. D. V. Shirk-, and Clowal MAL-jaml
X
d cook.. 51-oklal . two y`au-R-C-C5T~W-.o. scientists working at
.." Vnrs-6Z.Ct_y, doearlbvi investigations for determination
of Us Influence exercised by the Coulomb (galon) Interaction
Cart 114 cl
T. V.
TGjma=.1io1 explained to,!
g.0 on, saprocand.att"ty.
_
_
t_.f`"tbG_-GsIl.d G.12.. I- or the Dose
m
"
'
t". In wepmcanductors. P_ _9_ZWL-go. Uekova;1to.
spok.of the tAraody.asl~. of apmcna4aator. and J~_T.
1" of %he thorsel conduction of supra-
T-31tw=G, V~_7.9,saimaMwr reported on ex.
portmeat.&I work with suprecoaductor.. P- 1_7parArLtakly spoke
of the "ooor"Weet of the -1-tr.py of th.-I -d.ativity In
th go renanductl- tat*. Is & series of rop~to pxviAm, of
r
th: "rMlIqu.141ty of ballum were dimma.ed. which was dls~ov*~
ad in 1958 by P. L. I.Pitom, -4 the th.o'y or hich ..a set V
in 1941 by I. V. Landau. Z. L. A-.dro-alkA!hv -4 Lt. Gal-
laborstors Investigate d t.'s properties 0fmisting hall".
V. p"Fshkov spoke of the offset of Uld fo~tloft of the
bounder, be tooes, amparlIquid and non juporliquid belt". Goes
ym-.
cQII&%ovxtor
V.y
tho
ladtit4t ftXieheoktkh probleat
f
;
.
(IS tLut of PLY steel bl-)lavs-tif&tod the properties of
;r
o
e
I- p-tars of Upit.A. T- N. Llf,hLt,,
ue J-P
l:
i
.
-2-1-2AIChaawyIit 111*1 11 ph ....
. is
strong oacnetic fields far soUld with open Perot our Go$.
%
2. Is. Aleksayevokly, XR. ?.
S!ydukov *xp*ri.entally Invest%-
_04rd-2/4 __
salWatrojy-or-joid aonocrystals In the
ablao too presona. of
I S.Kan. S._O___L�q-v .
:
a "*P*r tr. ;inia" ;ilb. t";~%-.T tat. of the _MI.
Jt. ~jeort. d 0. the quentoo theory of saw a--
r
por- a. to. a.- I.-
A~~X
:
*.,F. V.tic ." I a of K.CO3. W. W. Km-wo,
p
the maga.tIc .4lantropy of ti. ~.11_
C-304 and C 50 a it h
a
I'k
,_
4*
J
ported troncer phic Inve.tICt:.as a t,.r, I.a.
~
a
,-Zam4amakly ad0Ilaborm.tor. reported on the smacepti.
Wility of n4ckol and nickol-copper alloys at low temperatures.
reported on kinetic pheacavea La
f.rro-Ca.ti . at Ice t.ap.r.ter... AL, I_4khjj-r. 1--a.
and spoke of c.p.t.tinns of the
_==:
the magnetic someat in f*rromaenotta dielectrics
at I.. tsapdr4 S&nadxo spoke of observation re-
-
_
raits of paramagnetic roic
a
~_e-eldf terbium In the TbJO 3 *6R20
Weis. rd.A,_AjL&AImhvIlj gave a theoretical analysis of the
:
rise tation of the nuclear spin In the Overhou.er (Overkhauxer)
effect Is A- I. Sws-ylal, S. U. 1-Y.G, Ad cGll.b.--
-
-
-
'
-
-
ct-
M
t
d
AI
rs rejor
e
on ob%a
n
c
rrQ
."tNd iu
.17
of
P.
C
dG~.!!!z~jmshov*d that hYdiAG*njot_QF4a-js
as . 1. he different ot;ucturwo. 1. A. GimAU, D. 0.
Lazarsv. Ah. D. StAE211~.QT zz~- T. 1. ZhGtkTT1Ch detected Vol,.
sorphims In a number of at I.. t.spe"Wr*.,
K. I.
.
_
Antronikashvill, T. P. Poshkov and !. P! Malkow reported on it,*
a, do
tags
vfl*Pa*nt of foreign sciont-aic research work in the
of lo
1.14 Conference
: of
'
of u do pa.nt of in ... ti.
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1
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.' "". of Sol*..-
of the a"' 1. k y. 3A)
:'
5h thy I re'.-Ity or Tbilisi
%Y
l
Valeer.1 a. . I as the b.il di at of the now rejoarch atomic
1
reactor .
ear Tbtl
1.t. 11)
24(3) SCV/56..36-6-10/66
AUTHORt Alikhanov$ E.. A.
TITLEt Neutronogralhic Investigation of the Antiferromagnotism of
the Carbonatos of Mn and Fe (Neytronograficheakoye issledo-
vaniye antif*erromagnetizma karbonatov Un i Fe )
PERIODICAL: Zhurnal eksycirimentallnoy i teoreticheskoy fiziki, 1959,
Vol 36, Nr 6, pp 169o - 1696 (ussit)
ABSTRACTs Borovik-Romariov and Orlova (Ref 1) already inve,-)tigated the
magnetic properties of polycrystalline MnCO 3 and CoCO 3' and.
1. Ye. Dzyaloshinskiy (Ref 2) published a theory on this
subject. Dzya.loshinskiy pointed out the connection between
weak ferromagnetism and crystal symmetry: In Mz-,-Fe-, and
Co-carbonates 3 forms of magnetic symmetry are distinguishedt
1~ the spins are in the direction of the rhombohedral axis,
2 the spins are in the basis plane and are aligned. along
the axis of the second order, 3) the spins are in the basis
plane and tn the symmetry plane. In the first-mentioned case
no weak ferromagnetism can be observed, whereas in the two
Card 1/3 latter cases such a weak ferromagnetism is found to exist. In
Neutronographio Investie;eition of the Antiferromagnetism SOV/56-36-6-10/66
of the Carbonates of Mn and Fe
the present paper the author investigates MnOCI 3and PeCO 3
by means of' the neutron diagram method with respect to Dzyalo-
shinskiy's lheory. A crystal powder was exponed to a mono-
chromatic neutron beam (X- 1-37 A), and the scattered neutrons
were recorded by a spectrometer constructed by Yu. G. Abov
(Ref 5). Th,.- neutrons originated from the heavy water reactor
of the ITEP AN SSSR. Figure 1 shows the neutron diffraction
pictures obtained of MnCO 3 powder at room temperature and
at hydrogen temperature. The latter is between the background
curve and that recorded at room temperature, and has two
additional maxima before the maximam of the room temperature
neutron diffraction picture. The lattice constants were deter-
mined as amounting to a- 5.84 R and a - 47015'; further data
are given by table 1. The structure of FeCO 3 -was investigated
in a si-iozite sample found at Bakal (USSR). Figure 2 shows
the neutron diffraction picture at hydrogen temperature. The ++
nuclear scEittering amplitudes o.r Fe++ are double those of Mn
Card 2/3 Table 2 oontains -the ce.1culatod and measured relative
Neutronographio Investigation of the Antiferromagnetism SOV156-36-6-10166
of the Carbonates of Mri and Fe
intensitim for the first group of peaks. It was found Lhat
in MnCO3 the spins in the antiferromagnetic state are in
the basis plane and symmetry plane; in FeCO 3 the spins are
aligned along the rhombohedral axis. According to Dzyaloshins-
kiy this vauld mean that MnCO3 has a weak ferromagnetism,
whereas with FeCO this is not the case. The author finally
thanks AcaaemiciaA P. L. Kapitsa for his interest in this
investigation, A. S. Borovik-Romanov for his valuable advice,
I. Ye. Dzyo.loshinskiy for discussions, Yu. G. Abov for his
advice in c.onnection with the neutronoscopio part; of the work,
and Yu. V. Sharvin for placing a special thermometer at his
disposal.11'here are 6 figures, 2 tables, and 11 references, 5
of which ave Soviet.
ASOCILTIONs Institut fizicheskikh problem Akademii nauk SSSR (Institute
for Physical Problems of the Academy of Sciences, USSR)
SUBMITTEDt February 11, 1959
Card 3/3
ALIMMIOV, R.A.
Anti ferromagnot i gri of NIF2. Zbur.eIrep.i teor.fiz. 37 m-4:
1145-1147 0 159. (14M 13:5)
1. Institut fisicUinkikh problem Akademii nauk SSSR.
(Ferrcmagnetism)
(Nickel fluoride-Magnetic properties)
s/o56/6O/'C38/O3/15/O33
B006/BO14
AUTHORz Alikhanovo R& 1.0
TITLEt A Cryostnt for Feutrono6raphio Investiga.tions
PERIODICAL: Zhurnal eksperintentallnoy i teoreticheskoy fiziki, ig6ot
Vol- 38, No- 3, pp. 806-'808
TEXTs The present pa er described a low-temperature (including the tempera-
ture of liquid heliuZ oryoste.t,employed for investit,;ating the scattering of
thermal neutrons on polycryste1line samples. This apparatusq which offers the
possibility of investigating r,eutron diffraction within a wide range of
Bragg angles (up to about OB - 450, corresponding to a rotation of the de-
tector through 900)9 is descrJted in the introduction, Inside, it has a
Dewar designed by P. L. Kapitfja,(of. Fig. 1). As was shown by a number of
neutronographic investigationc, thfa apparatus operates satisfactorily. The
background due to the aluminumi casing of the samples amounts to 20% of the
counter background and does not disturb the neutron diffraction picture. In
this instrument samples can bc. kept at the temperature.of liquid helium for
Card 1/2
A Cryostat for Reutronographiv lavesLigations S/056/60/0f58/031/15/03)
B006/BO14
48 hours. The amount of heliuzi required is 7-5 liters. Fig. 2 shows a typical
evaporation curve of helium from the oryostat (1-3 1). A thermometer, suppliei
by YU. V. Sharvin and exhibit:.zig a resistance which strongly depsndg on
temperature in the low-temperitture range was used for measuring the tempera-
ture of the samples. Fig. 3 SILOWS the calibration curve of this thermometer,
which is 192-3.5 'Mm large. 'In vome cases, sample temperatu3res were' also checkbd
during the experimentg for whf.ch purpose a recording potentiB..,-ieter. of the type
EPP-09 was used. The'author ff.nally thanks Academician P~ L,'.Kapitsa for his-
interest and Yu. V. Sharvin forthe thermometer supplied.-Th6rd are 3'figures
and 5 references, 4 of which itre Soviet.
ASSOCIATION: Institut fizic)te8kikh problem Akademii nauk .5SSR (Institute ot
4 Physical Probliz.9 of the Academy of.Scieiiaes, USSR)
SUBMITTEDs October 10v 1959
Card 2/2
8692?
S/05 6010-19/005/046/051
14,1100 B006%077
AUTHOR: Al!kbaii *w6w
TITLE; The Anti f er romagneti sm of C-,)CO 3
PERIODICAL: Zhi.rnal ;~kErperimerztallnoy ~, teo-re"'.chriskoy ftlziki, *,96o..
V02'. 39, Ncl, 501), PP, 1481 - 1483
TEXT: Th .e author raportE on tho inv-ast.1gq'-on of hydrothermically pro-
duced finely ~rystailine C,.)CO 3 samples with the help of nSUtTon refle.1-
tion experiments aL low tempax-al.ures. Ha re3aiv~d these samries fron.
1~ Yu. IkornikcvEL ~f the Inst1tout, kristal-lografil &N SSSR of
C.rys,~allogr-iphy AS USSR),~ Fig.1 sh,,ws a neutror r1eflezt.:= d1agram tak-n
at 4.20K. The position of the magretic moments was computed from thgse
results. The direction ~f qLn.4.ferrom-agnetism with regard To th,-~ rhomb,~o
axis was determin~-d from t.qe magnA,.A~~, 4-atersity ratl,.-~s and -i-. wa3 found
that the moments and the axi-ii ene--ios-i ar. angl.,) -7-~f (46-4)'. The
magnfii, ons `,11) and (100) (see. d~.agram r, ', -1 0, and
,ic a -d als
j -ansit`on f-rc,a.- 20A 1. c 4.'0K.
(211" showFd a deztreaae in intensity on ti
Card 1/3
The Antlferrpmagnstlsm- of CoCO,~
86929
S/056/60/039/005/048/051
07-
Boo6/B
The results are briefly d',scusaed applying the thermodynair..Jl- theory by
1. Yo,. D?,yaloahincjkiy, FA(r,? lllustzrat6s the 1)csitlon cf Lh4 wagn~~ti--
moment in CoCO- ao detElrir-nad experimentally. Amcng other th--.igs !,. waft
found that the :-~gnetic moments of the ions fall out, of the symmetry
plane by the angl*, 11 an estimate of this anglR resulted in (15 , 5Y'-,,
and a calculation of thlB angle using the data from absolute 116a8llre-
mc-nts (Ref.8) gave 70. The wathcr thanks Academ-.cian ?, L, Kapitsa
for his inte.res... A. S.. Bar-,vik.-Romanov and I. Ye~ D zyal otill inski y fc~r
diw~ussions, and N. Yu- Ikornikoy and. N, N. Mi.khaylo-v for preparing and
sorll-ng the sample3 and 1. P. Karpikhin for his experimenl.ul
S. D. Chetverikov, P. V. Kalinin, M. G. Spiridonova, B,, M,- Shmakin:
M. P. Orlovr., and V. 1. Ozhogin are men-.Icned, There aie '? figures and
8 referencee: 4 Soviet and. 4 US.
ASSOCIATION: Inal-itu", fi21cheskikh problem Akademit nauk SSSR (Insti-
tute of Physical Problems of the Academ.-vr of Scien,*-es
USSR)
SU13MITTED: August 26, 1960
Card 2/3
86929
3/05 60/039/005/048/051
B006YB077
NO
ze
12 14 15 is a V u u
Card 3/3
ell
Wi
0b
I j
Svi
-NII p ~6
N 51 Ell
I
M.
I.
H
14
Ito
ja 60
ALIKHANOV, FOAO
N~~iron diffraction study of soUd oxygen. Zhur. eksp. i teor.
fiz. 45 no.3012-814 3 .163. - (MVI 16t10)
1. Institut fizicbeskikh problem AN SSSR.
(Neutrcn diffraction examination)
(So2ld oxygen)
ALIKHANOV y I.R. A.
TILtrd lnturnat~onal Ct)nferance on Low-temperature Fhysics and
,t(,~innulogj. Atom. en,)rg. 17 no.1172--73 Jl '61+- (I-IJH,, 17,7)
f
zip -10-f-k-b- /64/000/066/6i
z 2 1
~Nrl W
OP,*.- M-Ikhanov~
WOW.
-AfffTLE: Neutronogravh,6 ij~lr6flt~~Ub:ns 'of SOIJI'd Ox
ygen
migiv--i -conferen RHO --and T
8-6u --~11 --Thy I ~'s LecbAjau-eE
e
P - 6~- 1963- Phyntos iqu-6-9 of 10-W-Abey tu:7eg; prooeedin
-L 0
raRe -M-freer-ence. Prague, Tubl. House of `,Mze
1-le Zeby)0917 emy o
-1.9ciences -~1964,---n
TOPI T 0 nou tron:- d*
iffract-,'1ioJ1i- solid ozygen- crystal structure
f P-
phase transition,.: low. tepperatu: esearch
_t4 t a -id oxygen were made with
Tq TRA,
an.. a
~v ad vis Ing
a
t --measu men"Us IlAne- an -magnd-ti-d-,'-Propor tie's d ~-vxyg.
que's o olf cryat 'I C'M
'low te
at. mperatures. Some. o ;the earlier studies are revieWed'. And
Abe di f1culties--of the rieseb-arth are wntioned. The technique used-
f
was descri eMilier (ZbETV.: v., 36 (1559) 1690,11J., with;
bed1by the author
AA
j
L T
!Aj
GOESSION-Nnu. :AT500044
ption or the, vnethod.-Used-~bf orklng~with condensed gases,~,", Ibig-'Z-f
entailed'tbe use of a Kapitsa-i6war tbe- Ii, ti n of wbiclo Was.
,apg. da o
The ciryostat-;.
Also deseribed binthe author' bET 06, ig6o).
Enclousre.- lituke of!,
~i-s~-1-:Lltibtrated-,In-Fi&--l-of t e An Important,'fe
th6_-'h6w--6rYo ta!~~_ -is _d J~A_ tz I-o f i-- a -q re e
_T-PavItxg-tbe-
Fit
isame 'te d' t _: 6hi the --t"
o urea. that-
~.pera-tux4e% as the -bath, a-use
the-~sample assumes - in stat t~Shion'':,:the $emperature _,ot the, ba
.'The ;meiasurements ~ of ~ the' n6utxioi ~.dirfiaction ~rrom oxygen.wem~,Perf d
Mlth't~e~-batb- -hiled with'-AUMId. neon hydroj~en, and helium. The
6sitions 6f,the-obtained diffloaation. line !ribed ~w 11: b
s yare desc
15 , y
Thoffthedral lattice witb pai~aneters a 4.210 and .8=. 46.*16 .- Dif-
_,:'fraction'Patterns obtained:ai einperitures sboited slinilar'
ivarious: t
behavior, but-differed- from t~'btt,.obaervati6ns made in the phase'.
nd
Thio. indidates. that, these. pallftjwn's belong to the a phase a ; irv lie a
alws-A n-Ahe- -tra, alm.
to U-I
_OX S_ ferromagne, 6-
Ind-lbatbb`tha 'a) U *lo- ~ I ,deeply-,
t --I.-ar- _~ra,
mo. Acad&ml ."Ka-
di z Oita6i j
N P~ ~Attentioall -ahd,.constant., inte,we-st.7apac
-A S.~ rovik'
t
o~ jlnskiy~.: for: fruitrul;-1
06
rd,
EW(-T)/FkT(k) JrS/J)D
AT6031144 SOURCE COM-i UR/3138/65/000/355/0001/0020
AUTHORf Alikhanoy, H.A.
ORG: none
-TIITLE: Inelastic scattering of neulrons Cy hematite
SOURCE: USSR. Gosudarstvenn:yy komitet po tspollzovaniyu atomnoy energii.
Institut teoreticheskey i eksper~mentallnoy fiziki. Doklady, no. 355, 1965.
Neuprugoye rasseyaniye neytronov gematitom, 1-20
TOPIC TAGS: neutron scattering, inelastic scattering, inelastic neutron scattering,
hematite neutron scattering, tricrystal spectrometer, hematite spin wave, magnon
moment
ABSTRACT: A three-crystal spectromete was used to investigate the spectrum of
spin in hematite o1 Pe'2 03 originating from the Shabra deposits. The experi-
ment was conducted over the 0. 64AO-2 to 5. 3-3 ev range of transmitted magnon
moment and energy. Two branches livith energy gaps characterized by magnetic
anisotropy were observed. Valves of (1. 3 + 0. 7)1(1-3 ev and (0. 4 + 0. 15)10-3 ev
were observed for the gap, and I'l. 3 + 0. 7)106 cm /sec and (4. 6 + CF 5)105 cm /sec
1/2
L 01239-67
AT6031144
for spin wave velocity for the b:ranches. The author thanks Academicians P, L.
Kapitsa. and A. 1. Alikhanoy for their continuous attention to this work, I. Ye.
Dzyaloshinskiy nd L. K. Fall kovskly-for their helpful discussions. Th-e author
thanks Professor G. P, Barsanc-v, and Vu. TI- OrIcur, V. V. Yakulovskiy, and
M. A. Smirnov of the Museum of Mineralogy AN SSSR for their many years of
assistance in the study of hernatite monocrystals, and staff members of the
Analytical Chemistry Laboratory of the Institute of Geochemistry AN SSSR. Orig.
art. has: I table and 6 figures. [Author's abstract) [SP]
SUB CODE: 20/ SU13M DATE: 05Jun651 ORIG REF: 006/ OTH REF.- 019/
2/2 *a"m
A~ "'; AT6033191 SOUI'~CE C'ODE: Ul-1-6/313~t)/G-J/000/393/0001/0015
AUTHOIR; Alikhanov, R. A.
L.rnirr.ov, L. S.
ORG: none
TITLE: Neutronographic inveiAigation of the low- temperatu re-Da n i t
in chromium
SOURCE: 'USSR. Gosudarstvennyy komitet po ispollzovanipi altoninoy cnergii.
Institut teoretichesho , clisperimentall Y fiziki. DoRlady, no. 3)91), 1965. Netrono-
iT --------- ----
graficheskiye issledovaniya ni.!-kotemperaturnogo magnitnogo lircvrashcheniya v
0
khrome, 1-15
TOPICTAGS: chromium, cryostat, magnetic transition, lowternperature.
magnetictransition, crystal spin structure, chromium crystal, neutron scattering,
maanetic scatterin,-r
t> t~
ABSTRACT: A neutronographic study was made of the low-tonverature magnetic
transition -in samples of crystrilline cbxomiuffi_c~ i1nd polycrystalline chromium con-
Laining cqual aniounts of imptiritios but. subiected to different thermornechanical
4.
Creatment. A miniature cryostat (wc-igght 530 g, hr-Aght 200 rnm) was used. The
CQ,d 1 / 2
I ACC'NRI AT60:33191
study showed that the transition temperature Tm increases with an increase in
metal plasticity, and that the sp: n dezis:ity modulation period and its temperature
dependence are a universal property of chromium. The authors than], P. L.
Kapits for his interest in this work Lnd 1. 0. Panasyuka, D. D. Abanin, T. I.
0 :-- -- ~ -
Kostin and T, 1. Kozlov for their assistance. rig. art. has. 5 figures.
[Authors' abstract]
SUB CODE: 20/ SUBM DATE: nonet ORIG REF: 0091 OTH REF: 009/
1A Ll D V, G-
SUBJECT USSR / PHYSICS CARD 1 / 2 PA - 1656
AUTHOR AMCHANOV,S.G.
TITLE A New Impulse Method for Measuring Ion Masses.
PERIODICAL Krn.eksp.i teor.fis,1j,faso-3, 517-518 (1956)
Issued: 12 / 1956
By the focussing method suggested bere it is possible to increase the re-
solving power of the spectrometer considerably. The mass spectrometer consists
of a drive tube which is limited on both sides by slowing-down fields with
linear potential distribution. The whole device is in a weak longitudinal
field. The condonsed ions produced in. an impulse-like source are Oinjected"
into the tube, and at the same time the slowing-down field is switched on.
The condensed ions inciding into the potential well begin to move from one re-
fleotor to the other, on which oocasion the time gained by the fastest ions
with given e/9 in comparison with slow ions is compensated by the loss of
velocity during motion in the 31OWiag-down field. The ions with equal 9A
and different energies then gather at a certain point in the drive tube.
After a sufficient number of cycles, when the ions with approximately equal
e/M separate, the shift of the time of arrival in the focus exceeds the time
needed for condensation. Hereby the latter are deflected and annihilated. In
order that the condensations oJ! ions with different masses osoillate in the
tube, it is necessary to conneot a roltage on to the deflecting plates which
is switched on only on the occasion of the passing of the ions with the masses
to be measured. For the duration T of a complete cycle
V
Zurn.eksp.i teor.fis,31,fasc-3,517-518 (1956) CARD 2 / 2 :PA - 1656
T = I V-2 M/uze + 2((l/E,)+('/E,)) V2U7M/Z is found with the slowing-down
fields EI and 22* Here M denotes the masal Ze - the charge, and IJ - the energy
(in volts) of the ions, and 1 - the length of the drive tube. The condition
aT/aU results in (1/El) + (1/B:2) - 1/2 U . If the suitably selected quantities
U , 1, E1 and B satisfy the latter equahon, a grouping in time and in space
(2ocuseing) of he first order of ions of differeht energies is attained. How-
ever, the focussing condition of the second order is not satisfied and the
washing out in time of the cycle for ions with the same mass is
A TU (1/2)Y M/2ZeU1 If),. The limiting value of the resolving power is
0
A (1/4)(6 U/Uo )2. The accuracy of measurements depends ort the duration
and the linear dimensions of ion condensation. Tho ratio (duration of ion con-
densation / time needed for paosage) must be smaller than the limiting value of
the resolving power. In order to improve accuracy it is necessary either to in-
crease the langbh of the tube or the ions must perform the necessary number of
QY018B. The field strength of the longitudinal magmatic field is selocted in
such a manner that the resolving power of the device is not diminished by an
increase of light intensity.
INSTITUTION:
4,t~J
. . . . . . . . . . . . . .
-0: mT~
41 4-T
F.4-o vz~.r -~,,~j va
1. A 'I Y -X
m-, .4%,Xz a~7,yj
0:-r3 -o
.rzow K53 /4 zvn~,Tc.(.
lz 41 171-u 11 a q
~-.,j
5,z-.,xnDl nz~D 30 Q, ~-t c Z.I~ Y.
.V"
U IL P n! C A -9
s v r u -71~v o 9
~Azjj
uu;nz V.-.ao;ow3 gzulr
;o
5 q q
svL) ro~;j-:-,t4a e4Tjojj v al QTawtzvja oaT,,l v in rol-wnly-al.
Mrpv... 1 A p-a 7--,,*':77:4 j A 173-aw~-.-v it v ,--T, -,&t-Z'wj v 0 a
F-.-J-4
,,,,; ZAKWOV, V. Yo.; KHORASANOV, G. L.
A ANDI, S G
Plasma difftsioli ia a magi2etic field caused by Coulomb
collisions. Atom. tonerg. '14 n,6.2:137-la F '63-
(MIRA 16:1)
(Magnetio Molds) (Plasma(Ionized gases))
(Coll.4~sions(ffuclear pbysics))
ACCEUM NR# AAM260 9/0207/61VIMA W /006
AUnMe A3Ubow# lo Go (Nov"IbArsk)
'TMAi Investigations of week2y 14misod hellum plane diffusion in ik mapotle
field
Al pri". "MM., J. towin. fis.; no. 1'p IL9649 IM-A.
IMMS, ZWWr
TOPIC TAGSs holium plasnap p1mia d1fAssions magnstio field,, snonalows diffusion
coefficientp turbulent diffusion, lon dwlft
ABSrRACT a The decay time of a bellum plasm in a 0-5000 oersted mgmstio ftold
!has been investigated in a tbin tabs with R w Oo8 =4 L a 80 emp at yzesioures p
to 0*2 ma Hgj and electron conoentrations of 3.0 to u4ce% no diftu
Ion
cooffioloub In Us p3ma is date,-Wined. by measuring the decay time -according
'to the axpmuica
2.4
+
Aoil- 540 CAAMP-1 Ax pr. er.9
6- Jr'W
cc,
rd 1/2
AG(;=oN NR s AP4022655
vhwe Dsj Do coeffJoient of ancmLlous CIfusion and diffusion in absonce of
magnetic field at I m pressure reepectivelye The results obtained wtierimentany
ical H-2 diffusion law. To explain this
show a significant departure from Iho class
discrepancy D,, is calculated on tbe, baeli; of binary colliaiorm and iB compared to
the experimental data* The resa~ shows D. to be related to the magnetio fieaA by-
the law Dg , l/H independent of the plamma prhasure (0.05 - 0e2 m Hg) & This affect
corresponds to the turbulent plasia diffusion theoz7 on drift wavea of BagdeM and
others* "The author is grateful to P, Z, Sagdayev and So So Noisaywtor evabating
'the results wA tb"r h93pfvI discassiows and to Oe Lo Kbm &wv and (1, 0
!Pod-losmsy for their bdp'la the uperimentset Orig* art* h"I 5 fMNIUW and 4
figures.
'ASMUTION I Am*
!8U&WM I 06pnO jWQI
CMI Cr M In, GOV# IMM 0*
CIiwd tit
ozk
it
pTFFX"y ---I~
'44yor A-VA41 , I iro
-6'd
h9l O'curvc, S1.
wit
ON
acc
e ;C a-
liii6~ ith th i 'S'sibid
Y_
r Io
tran'spo ~t coeirficlonts pr"iio 'n
p
,194
L I
Category: USSR/ Farm Animal DisFaoes Caused by Bacteria and Fungi V-2
Abs Jour. Refer. Zhur-Biologiya, No 16, 1957, 72308
Author Gryelov V. P. Alikhaaa,fa Kh. M.
Inst Not given
Title A Case of Actinomycosio of the Breat-Bone of a Cow
Orig Pub: Tr. Dagestansk. S.-Kb. In-ta, 1956, 8, 193-1-94
Abstract: In the region of 6-7 segments of the breast-bone and 7-9 rib carti-
lage a painless swelling was found, which had a pus secreting fi-
stula in the center. The study of of the pus demonstrated the pre-
sence of actinomyces. On the basis of the findings, upon opening
the authors suspect that the actinomyco3is localized in the breast
bone occurred due to a trauma (piercing of the bone) by a wire co-
vered with Actinomyces, which penetrated into the breast region.
Card 1/1 -15-
ALIKIIANOVA, 0.1.
Increasing the pr,.-cision of the spectva2 llstc-rmina~ion of boron
in soils. Zav. lalb. 30 no.J.,47 "- 61. . (KIRA 17:9)
1. Nauchno-issledovatellskiy Inatitut pochvovedeniya.
ALIKRANOVA-
froblem for a functio4al equation. Dokl. AN Axerb. SSR 5 no.5;371-374
'59. (Integral equations) (Mlllk 12:8)
AGAYLV, G.N.; ALIKHANOVA, It.X.
Cauchy's problem fc(r a functional equation. Trudy Inst. mat. i
iekh. AN Azerb. SSE. 2%129-132 063. J'MRA 16slo)
ALIKIIANOVA
.1. - - I.-A- -I. -
Cauchy problem for a quasl-yirabolic- Equation,. Doka. All Azerb.
SST[ 20 no. 6',')--14 '61, - (MIRA 17;90
1. Institut inatemat."ki i mehhuni-k.l. AIN AzerSSM. Predstavlenc,
akademikam AN AzerSSR 71.1.ftahlovym.
ACCESSION MR: AP4045055 S/0249/64/020/006/0003/0014
AUTHOR: Alikhanova, R. I., Khalilov, Z. I.
-'FITLE: The Cauchy problem for a quEzi-parsibolic equation
SOURCE: ANAzerbSSR. Bo)dady*, v. 20,.no. 6, 19G4, 9-14
TOPIC TAGS. Cauchy problem, parabolic eqtatlon. quasiparabolic equation
ABSTRACT: In continuation of earlier work (Agayev G. N., Alikhanova R. 1. Tj,udy* in-
ta materiatiki I mekhaniki AN Azerb. ESR, vol. 10, 1963), thb author consWers the
Cauchy problem for the functional integ-rodifferential equation.
-du(t, x)
dt .;W [ I u'(1,Qd( A,(t)D'*u(tjr)
with the inital condition
where % is an n-dimensional Euclidean space. It Is assumed that
04
Card 1/4
(2)
(3)
ACCESSION NR: AP4045055
where C '*0 is a definite number, independent of t and z. 1%e form
0 Q m(z)A.(t),p1 (4)
then d6creases monotonously in z with fixed t and a real vector p. The solution to sought
in the class of functions vanishing near idialty. together with their derivatives of the
order > 2r-1, and reduces to the soluUon of a dual problem. It can readily be demonstr-
ated that if
I(F.
q4t, P)
and v(t,p) Is the solution of the dual problem
dv(t. p) (6)
dt
with the WURI condition
(7)
2/4
Card
ACCESSION NR: AP4045055
thon u(t,x) Is the form9l solution of thEl problem represented by (1) and (2). Assuming that
(8)
P
where N 0 is a definite number, It Is ~Aear that the Integrals
Sit+ I 1'1j2r+A+1 (9)
p -fq'(pjdp
and
(10)
converge. This Is proven by means of four preliminary lemmas. The author then goes
on to prove that the problem represented by (6) and (7) has a solution, arrived at by the
inethods of successive approximation and mathematical induction. In final forn-,
required solution of the problem reprehented by (1) and (2) is shown to be
U (t. it) V(t, p) --)dp.
'71 t
Card 3/4*
ACCESSION NR: AP4045055
"The author expresses his appreciati,)m to G. N. Agayev for suggesting the problem and
helping In the daily work." OrIg. art. has: 12 numbered equations.
ASSOCIATION: Institut matematiki 0nekhaniki Akademii nauk Azerbaydzhanskoy SSR
(Institute of Mathematics and MechaWas, Academypf Sciences of the Azerbaidjan 88R)
SUBMITTED: 02Jul63 ENCL: 00
SUB CODE: KA ]K'0 REF SOV: 003 OTHER: 000
Card 4/4
ALIIMNOVA, IJ.M
Treatment of thin severe form of trachoma using cortisone,
ronidase and ettizol. Azerb. med. zhur. no.10:57-61 0 161.
(MURA 15:6)
(CONJUIXTIVITAS, MANNUIAR) (CORTISONE)
(ETA2',OY,) (HYALURONIDASE)
S/078/61/006/005/004/01.-O
B121/B208
AUTHORS: Markovt V. P,# Alikhanova, Z.M.
TITLEt Uranyl oompounds with trihydroxy-glutaric acid
PERTODICALs Zhurnal neorgarticheskoy khimii# v, 6, no- 5t 19610
io66 . 1073
TEXTt The complex formation of the uranyl ion with trihydroxy-glutario
acid COOK - CHOR - CHOH - CHOE'- COOH was studied by physico-chemical me-
thods such as potentiometrio titration, determination of the specific elec-
trical conductivity and transference number. The potentiometric titra-
tions were made on the AIT-5 (LP-5) potentiometer by means of a glass-
and a calomel electrode. 7ae titrations were carried out with a 0,1 M al..
kali hydroxide solution and mixtures of 0*1 M aqueous uranyl nitrate so-
lutione and trihydroxy-glutaric. acid with different ratios of the com-
ponents at 200C. No hydrox:1de precipitates in the titration of a mixture
of uranyl nitrate and trihydroxy-glutarie acid with alkali hydroxide so-
lution. It may be seen fron the potentiometric titrations and measurements
of the specific electrical coneuctivity of isomolar solutions that tri-
Card 1/7
B/078/61/006/005/0%/015
Uranyl compounds with ... B121/B208
hydroxy-glutaric acid reacts with uranyl ions by forming complexes in which
the ratio of the components Vt C 5%07 varies from 1 : 3 to 2 t 1. Various
uranyl compounds with trihydroxy-.glutaric acid were synthesized.
UO2C 5H60 7.1 1/2 H20 is obtainad by two methods, In the first method tri-
hydroxy-glutario acid is aldett to a nearly saturated uranyl nitrate solu-
tion up to a ratio of the ~3om,~onents of 1 : 2. After 2 - 3 days a fine-
-crystalline, light-yellow procipitate is obtained. This method is also
applicable when using uranvi ahloridef but not, when using uranyl sulfate.
In the second method# trihydroxy-glutaric acid is added to an aqueous sus-
pension of uranyl oxide in the, heat up to a ratio of the components
U S C5 H807m I a 3. The aLalytical results ottained for the crystals pre-
pared by the two methods are the oame. The crystals of U02C 56'7' 1 1/2 H20
are insoluble in water and organic solvents, The compound
002)2C59407-020 is precipitated from a solution of uranyl nitrate and
trihydroxy-glutario acid, w:aero the ratio of the components is 2 1 1, by
a mixture of ethyl alcohol f2 parts) and ether (5 parts). Chemical ana-
Card 2/7
S/07 61/006/005/004/015
Uranyl compounds with ... B121YB208
lysis confirmed the given foriaule.. The compound is soluble in waterp but
insoluble in organic solvents, it is decomposed in aqueous solution by lyes
or acids. The compound is a nonelectrolytep as was confirmed by measuring
the molar electrical conduotivity. The compound '(TJ02)2C5 R60 7(HSO 4)2 on20
is precipitated by treating a solation of uranyl sulfate and trihydroxy-glu-
taric acid with alcohol and.ether, The chemical analysis of the compound
confirmed the above composition. The compound is very well soluble in
waterp but insoluble in organio salventso The compound
Nil4 (UO2)2C5H30V3H 20 is precipitated from an uranyl nitrate solution with
trihydroxy-glutaric acid at a I)H of about 2 after 2 - 3 hr in the form of
a fine-crystalline, light-yoll