SCIENTIFIC ABSTRACT ALEKSEYEVA, I. - ALEKSEYEVA, K.

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• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R000101010003-5
• Release Decision: RIF
• Original Classification: S
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• Document Creation Date: November 2, 2016
• Document Release Date: September 24, 2001
• Sequence Number: 3
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

AT-RI; HYLVAS T.A.; SPASJIUY, 5,~.
Lwasitigation of polywre of polydiethylene glycol fup"arate and
copo3j=ro of polydietbTl*ne glycol fu"te with styrene
by moam of infr*red spectroscopy. Trudy KomjUi-&4khJn- 13:
356-~59 163* (MIRA 16:5)
1. Institut khivii Urallskogo filial& AN SSSR.
(Diethylene glycol) (Fumaric acid) (Spectrum, Inf "I

ACCMSMM NRI AP4017638 S/0190/64/006/002/0265/0268
Senerneva, 0. A.1 Samarina, L. A.; Bulatov, M. A.;
AUTHORS3 Aj6ks2;*Xtp
TITL$t The syntAssis, polymerization and copolymeritation of polyorganosiloxams
coataini;T4 rattacrylate groups. 2. Investigation of polymerization and copoly-
n*rlzation by thoo infrared absorption spectra method
SOURCE& Vy"okmolokulyarayr" soyedineniya, Y. 6, no. 2, 1964, 265-268
TOPIC TAWs organosilicon ccupound, organo*iloxane. polyorganosiloxans, methacr7-
late, styrene, copolymer with styrene, methacrylate polysiloxane polymer, double
bond, xaturatica of double bond, infrared spectra, absorption band, absorption
-band optical dowity
ABSTRAM Block polymerization of methaerylate polysiloxane3 (containing frcm zezo
to nine of the SA(M.3)20 groups) and thair copolymerization with styrene (in a
ratio of 2 Mal or styrans monomer per I Mol of polpiloxane unit) were investiga-
ted. The polymerization vas corkdacted in the presence of 0.2% benzoyl peroxide in
sealed ampules, In an atmosphere of nitrogen, for 6 hours at 70 and IOOC and 12
&prs 320C, vhen it underwent complete solidification. The infrared spectra

ACCESS30N MRs 06017638
were taken Vy moaris of a IKS-14 registering spectrophotometer, the absorption band
at 1634 4PCI having been selected an representing the CH - C - double bonds which
decreasq In nmbm during the reaction process. The o1r band was the one at
697 ce,64 vUeb represents the Si(CK3)2 groups, the nmber of which remains conf-
stant. As can be seem frm Fig, I on the Enclonum, an increase in the number of
mtbylgUmmm groups caw" the optical density ratios to dmp due to a decrease
In the double bond content. It Is sugg"tod that the presence of unreacted double
bonds Is due to staria hindrances. The copolymoritation. with styrene was found to
proceed towardaj *A alwat campUte saturatica of the double bonds* Origs art*
hAs 1 2 charts wA I table &
ASSOMOZONi Institut. Mali Ural'skoco fl'41mls AN SSSR (Institute of Chamintr7o
VrmA XvIision AN-SSSR)
SUMOM 03CI"62 DM AMP 2.1tarNs. ZRCM M
SUB ODIDU al NO REF SOVj 004 On=$ 002
.1..,
c.j 2/j'

MCQX,HAHOVA, Y.V.1 MAJUSNIV., V.G-; ALUSH-16VA, 1.A.
OrtimUng ofreet In the muthylation of beny.-me by methyl
hloxidu.in the presence ur altmCnum Chloride. 12v. Sib. , t~d.
JJI SSM to.3:80L-83 162. ( WYRA 170)
3. JI-all'skly filial AN .~S.;X, Svitrdlovek.

SEMENEVA, G.A.;SI:VOIIO';, A.L. SAMARINA, L.A.; ALMSEYVA, I.A.; SPASSKIY, S.S.
Infrared spectra of sozae organotitanium com ds. Zhur. prikl.
scoa.t. 3 to. 6t555-559 D 165 r1ria 19:1)
k, S%ilrltt,!~d 0,1,ober 9, 21'4-4.
I

FIJAPPOV;., M.N., inzh.j PFN-F",CV. V.%'.. A:,E*~"F~EVA, T.D., inzh.
distribation tollwepn ,f power
plmnts. Elek. at&. 36 Y 165. (MA 18j4)

ALtK='h'VA N.V., dcts., kand. takhn.
.'-*,-,,""***'iiibtf,"'~;otsonzakit; UMANSKIY, G.A., inzh., retsenzent;
AMIENOVA, r,.A.,. red.
jniji:tr3,.-aI wA magnetic mearumments In railroad transpcrta-
tiond Elaktrieheskle I magultMo iumerenila rA z4-clsinodo-
roalimum transports. Moskv&, Tritnuport, 1965. 227 p.
(HEM 18; 8)

YANOVICH, T, D. I rAIJMOVA, 0. N. I I.K.; RACHXCVSKIY, A.P. I
05-MINA, L.A,
Study on tuberculosis infection bor mmans of graduated epicutaneoua
tuberoulln test. Sbor, naucb. trud. R*st. goo. mad. inst. no.220-
12 163. (MIRA 180)
1. 12 'kafedry epidemlologrii Rostovskogo gasularstvennogo meditainskogo
Instilutit (zav. - prof. T.D.Yanovich).

r_lpiyworgumc unametv,
Alhs No (~5'j 16847
Wthur X.3 Ytajmirskl~, I.T. lllekseye,~a.
rnst
V tle Stlidy of Oxalat,_- ri.d Phozlih-te Compl--xes of ?4D].y-
bdim,um by th,:~ )LnLtl~_, Mai.hDl
Ori~,,, Pub Zh N~,or~jvn Kim!! 1950 -- No 5 052-S5f
lb s t r-,,. c tThe ,quilibrium in solut- ons o.' oxal te and phos-
j4r.te ccaplexos ol' bin vis attillcd on the b-isis of the
vie, surcm-out of th ~ speol of the rot ~,,Li oit of iodide
ox~datio,I 1%; h.~drc) va porox:,da Li an E.aid M-clium.
71,,"s reat,*tion is t_ly4ed. I-,- noly)Alc acid (T)
M19(him 1.1.56 -ju .5,'. A &2,:.-eare or the concentri-
tion of I In C0113eq,ae:-ce of the formt.on of complex-
e3 ca,ascs a carresijoilding ducrease o~' the reaction
speed. Qx:O~ic al plIonlihoric ucids vere used in ex-
cer,si c Lmowilz tz c-&i-ex producin.., rop,,-,ents The
miceiAr.,tion of' tne Ht ioiis wt,.s O.lL4 M'llie kine-
tic s-,udy shoved I r~-:_(Aed w:th ox:-,Iic acid ac-
cordln~- to th,! :qu-1, ca: H24.0
4' V~04 Cl~W2CL1041
Card 1f2 -2o-

USSR/InorgttnIc Chumistry. Complex Coiq)nujids.
Aba Jour - Wfarut. Zhunxil Yhimiv-.i 1-0 6 1957, 18824-1
+ 2H20 (1). The eqktillbrium constant of the reac-
tion (1) is 2353 :t 120. Phosphoric acid reacts with
n ta i one :
(I corl? to th oqt t H2MO04 -f H3PO4
2P04- -" H ~1~ (2) end H2M004 -+ 2H3PO4
~i'xoc) n2j4-+-4U*42H20. The equilibrium con-
2(rol, "
at-Ult of the reaction (2) is 10.5 t0 '(~ it was
fowul ttkit H4CMo02(PO4)2J (II) is a strong acid,
and the value of the cohStnnt of cUssociation into
simpIc compounds w-As alao found. The values of tha
equilibrium constants refer to the temperature of 22
to 23' ruld to th~ Joit of 0.46.
Card 22/2 -zi-

Atnmm- Yataimirsk:17, X.B.. Alelwayeva, I.. X. 153 -58-1 -d129
TITIS: The Investigation of Absorption Spectra and the Determination
of the Dissociation Constants of Holybdio Acid (IsucbenVe
spektrov pogloshoheniya i opredelardya konstant dingotsiataii
molibdenovxV kisloty)
M ODICALS Isvestiya vyushikh urhebnykh zavedeniy Xhimiya i khimicheakaya
tekhnologiya, 1958, Nr I , PP. 53-58 (USSR)
ABSMOT: A prooess of aopolymsr~zation is assumed to take place durIng the
dilution of molYbdio sold solutions. and it is believed that
highly dl-luted solutions conteLin nearly only monomeric particles.
The correctness of this assumption in confirmed also by the stady
of owplex molYbdern- compounds (by the application of the kimetio
method). The authors were therefore interested In inveatigating
these diluted mDlybdic, &old solutions by the optical method. They
obtained the following results% Highly diluted molybdic &old solu-
tions contain no polymerized parti:les, which proves the constancy
of tha molar extinguishing coofficient within � fairly a tensive
interval of the molybdenum oon..vntrates (2-10-~ to 2-10-4 X). :By
Card 1/2 the kinetic method it was established that in acid solutions and

The Investiption of AbsorptUm Spectra and the Determinatir-
of the Dissociation Constants of.Volybdio AcId .153 -58-1-8/29
in tho woo of a high degree of dilution mainly non--dissociat4d
molecules of moljtdic aMd exist. It may therefore be expected
that in the oame of low pi!--Yalues non-dissociated mr1ecules, tout
at higher yH-values Wromolyboiate- and molybdate ions ed-11 bit
found (as dissociation products of molybdic acid). For the de-.
temination of the H2~~I+,%iisacciatior, constants and for the Iku-
]POO* Of inVentigating the absorption spectra the dependertoo of
tile optical density of tht solutiome upon the concentration of'
th: WroMen ions was studied. Aoo,-rding to the oourse taken 1-Y
th curve (fig.1) the existin-* OC 3 kinds of pamicles with
diveriie molar ortinguishing aoeffiaii,nts &coording to pH values
=at be expected. On the strength of the experimental data ob-
tainea absorption spectra of molyWic aoid as well as of dissoci-
ation products wert obtainei (fig-3). Thoire are 3 figuresit, 3
tableii, ana 6 referenco-,5. 2 of whi~:h are Soviet.
ASS001MCN: Xa&Ara ana3iticbPzkoy kkimii (Mair of Inr-lytical
ChezLdstry)
SUBLITTED:
Card 2/2

AL a k Se. ye --------
a-i
!23 1, - .1 1
j
.11 .1 ! j, ! ji
-1 Z
Pit
Hir-1:1--a
jai!
It 1: 1, 11.4 1 h2v lap
h flu"

5(2
A j 7HORS a iatiulmir8kiyo i,.b. , Alektjeyevu -' I. 3~ V/ ' 2 - 24. - 11 i -2/4
TITLE: S.Fiir troFho tome t ric and Kinetic Methods f3r Determining Molybderum
in Alloys (Spe-;rtro!'ct=etr1cneukiy --' kinetiohestziy metody opre-
d,?1eniya mollbdena v Bp1ava;:h)
PER10DICAL: Zavotiakaya Laboratoriya, 19~8, Vol 24, Nr 12. Pr '427--429 (USSR)
ABSTPUCT: A met.hod for determining molybdenum in steels and nickel alloys was
d-eveloped which is based upon the absorption of light by molybdic
ac-id in the wave-lergth region 220 - 240 m.~t(Ref 2). It is carried
-,),.it; in alkalkne medium. The sensitivity of the method is given as
7.10-7 6/x-1 No. The measurements were made with a SF-4 apeezrcphoto-
meter. The molybdenum content is aetermined on the basis of a standarc
curv-D. Yolybdenuz alloys of Ni base Nr 3 and 4 a:3 well as E,1401 and
KhIOS2btzteels were analyzed (Table 1). The relative error of ~he meti,
~-s 2-5 %. Tne kinetic method of determining malybdenum is ten times
-Dve sensitive then the spectrophotcmetri(. methoi. The prinoiple of
tnfi winell,~ --nthod is the catalytic effect cf' molylvdic acid in the
o xidation of i,dide with hydrogen perci-ide. The method was pre-
vi.k-joty rep~jrted in an earlier paper (Ref
Card SL11-10 Fe CU 2% ani ither iono axterfere in analysis "he iroy

SOV 12- -"1,;
sps~-(,'T "I Ih: vi c and K-4r.44 tic Upt~ic Is ;'r,r D- ne Kc -, yl A I loys
ju': the present t,-
an! t--und in a rcrplux A nK-M apFara:~,Zi '?.az ~--Se.d
Kh IOS 2 1 ntepl ~ To ble -I und z,. cxl,!,~ Fe~,OA
I
Th-1 vnn!-~~ t- vity c1' thr, zettod I s Sl-ut 1%-.)- 9 There are
tatili~s alli 7 ref-arenicass, C, ~f wh-.cr, are Srviet.
ASSOCIATI.ON: jhim;-~llo-teki,.!.,-].,-,g:.,~heskd.y incti tut
Te,-linolci6inial lns*ivate
Card -l"';2

AtWFIEVA, T. T.: Mpksttw C!hem Se! (dirs) -- "A nlu,9,r of t~i- pro-,*rties of
molybdic acid nnt its complex comporunds in solution", Tvnwvo, 19~;Q. 1P pp
(Min Hl,~Jmr Edue *M,*T,,, Mtn3vo Chm-T-mc*.-L Tnst), 11~0 cvpI,!-S (KL, wo r, 10,5.9, l05)

SOV/178-4-4-18/44
AUT~ORSI Yattimirskiy, K. B.,-Alekoeyeva, 1. 1.
7 17 1. State Molybdic Acid in Wi-ui Acid Solut'or.0
'Ibdentv~;y klisluty v F-ookislykh rasiverakh)
FDER:ODICAL~ "h,;rnal neorg&nicheakoy khimii, 1959, Vol 4, Nr 4, pp FIG-822
(!USSR)
LBSTR,LCT: Tho Goniitions under whinh molybdic acid polymerizes wer" in-
ti t d at different concentrations (2.0.10-4 t,., 8.0.10-2
arrand at various pH val,i-s (1-6.5). In order to as,,ertair.
t'.-.4i F:;snibility of the exis-zen-s of the monomeri- fcrM Zf
Mc,;bdo a:id and to determine the nature of the polymerization
process the light absorption of solutions of molybdates and
molybd.',.u acid was stuciied at wavelengths from 270 'to 350 MIU-
Tho letermiration of the ~.ptical densities was carried out
using a SP-4 spectrophotometer. The dependence of the mclar
abborption coefficients -jpDn the --nalybdate concentraticz- ras
4r,restigated at constant pH and constant wavelergth. 'he
c,~!iainpl sho-s that at 1cwer molybdate concent_lati~:%Zj
malybdin. acid is present in the monomeric form. The pc,lyme:--'c
form exists also at higher concentrations. The phaae 6_*agram

Car'. 1/2
of molyb-lic acid in solution was constructed .1
(log C i_

State hlzlybdic Acid in Weakly A.-id Solution
SOV/78-4-4-16/44
dependenoe upon the PH val-je). In the PH range 1 to 4 t..e
po',ymoriz&tion begins at a mclybdic acid concentration cf !0
MC)Iar. With an increase In the PH value the polymerizaticr.
bo-IlLdary shifts to the side of the higher concentration.
Final'.y at PH 6.5 no more Polymerization occurs. The fc11zw-Jrg
pclymerization schemes are suggested for molybdio acid:
nVoO 2- + (r-1)HOH;;;=(HUoO ) moo (n+1)-+ (n-l)OH-
4 4 n-1 4
r,~ PH values 4 to 6) and
(n+
(n,l)H, + (HMOO N moo (H moo
4jn-1 4 2 4 n
(at ~,H values 1-4)-
Th---~re are 5 figures and 7 references, I of which is Sc%riet.
ASSOCIATION: Iva:~,-vskly khiniko-tekhno1ogicheskiy -Institut (Ivan---.: Ch-m-. i
Techx,clogical Institute)
SUBM17TED: April 24, 1958
bard 2~'2

YATSIXEiMlY, I.B.; ALINKSEYPVA, I.I.
Spectrophotometric t1tration of lead with molybdate In the
ultrimlolet. Zhur.aml.khim. 17 no.5074-578 Ag 162. (KM 160)
1
1. Ivanovo Chemico-Tachnological Institute.
(Load-Spectra) (Holybdates)

TATMIRSKIT, K.B.1 ALEKSEYEVA. 1.I.
Absorpt1cm spectra or Isopolymolybdanic acids In solution.
a.w. morg. klim. 11 to.11-2513-2517 N 163. (KIM 17: 1)

AL'*!(,hT6"VA, .1. 1". ~urld Illed ~~ai -- (Ilisn) "Bioelf-:1,ric - :' -,f tfie cortex
nr.a tho sulmortiou.1 forriations of th,~ :-,-rrbruin in i-he l,i:,,,in, i,~r of experinental
Litt ij~.i -- tiar.." lw: I , 1 ~: 1. ll~ -vi
. k
3" te 139d 2'*`,' c07SEM (KL. 106)
-104-

of.difflorent atad &bordu2in Ust for the exaMnation of
tM1140 Mg AW~sout: for %dorouleals. $bor. samb. trod. Rosi.
go"." luts t16022tw9a 163'. (MIRA 18M
is k~ftft "100vialcall Rost"dkogo ""darstvannoto waitain-
sittlo thatitita (MT. - Prof. T'D.1towilah).

ALUSMNA, I.M. [Alekidileva, I.M.1
Obrreltitim batw-oftn -rntmin c~hftnpes In tho l,lo"i serum ani ,Ariqti,n
of thm arteritil p"asivre In ht%6,nrcitic.,z:)trirsrtini,,n shock. Fiziol. zhur.
(I.-kr.] 11 no.ltl2l-121 Jn-F 165. WIPA 18t7)
1. LAborntorlys izllc~nn~y-t bloloa-~~hnskl Ftvtivriykh -flich~stv In-
SUNtIA r.121010iZil. im. p ~11
~, AN Kiyev.

L 312BL-0
^CC NR, AP&Mla SCURCS COM UR103001651071002102261G230
-!Oil Physiolopy im. A. A. Boamolets, AN U!qn�~R, Kiev (Instytut
ORGt rVilt
fitiolohiyi AN
TIM.- Protein ahmn in the serum of the recipient after transfusion of a protein
_;s
(BKg
blood M!~*titutq )
SOURCEt UkrayinstlW blokhimichMy zhumal, Yo 37t no. 2# 1965, 226-230
TOPIC TAGSt protein, blood, serum
ABSTPACT3 Previous investigations of the author have shown that transfusion of
BK-8 (belkov.V krovosamniteV -.6; protein blood substitut"] induces a decrease
In the albimin content and an increase in that of alpha- and beta-globulins during,
the first five minutes - one hour after the transfusion. This report deals with,
studies determining protein composition of blood serum five minutes and one hour
after transfusion of BK-43 under conditions of precipitation of BK-8 proteins chances
noted in the protein formula disappear. 7"mrefore, it can be assumed that the changes
in the protein content of the serum - the decrease in albumin content and increase
in alpha- and beta-rlobuliln content - are asocciated In the early post-trans fusion
period with the transformation of protein fractions due to the transfer by them of
some of the blocd substitute proteins. Orig. art. has: 2 tables. [JFR3)
SUB CODE: r6 / SUBM DAI-E: 07J;in64 / ORIG REF: 005 / OTH REF: 001
Cara VI

t ",.ic.lon v:r pmtwin Krod isuba titaLf,
(KRA 113t6)

AUMMIVA, 1.14. (Alakeleleva, I.M.]
G,Vanges in nor= proteins follow-Ing blood lose and subsequent
tra.t.-il.',asian of the BK-R rTotein blood subigtituto. Fiziol.zhur.
I Q i-. 1 9 no. 51673-682 S-0163 OMYRA 17 CO
1. Lab,.-iratmrlyu po virabannyu dil bi.,.)1ogichno aktivnzikh rechovin
Lisl;!t"tu flEjologji ims 0.0. Bogamn-1.1taya AN URSR, Xxir.

=09MA, IJ. (Alebmieleva, I.M.]
Chang% ia the total -zoncentration of protein and protein
fractIons of the blood serum in the organism during repeated
adaWatration of the blood protein substitute (B"),
hatew-ogenous and isogenous serwas. Ukr.bdLokhim.shur. 34
ao.602"33 162. (MM 16W
1. A.L.ftomolets Lwtitute of "Iology of the Academy of
Scienmen of the Wa4daian S.S.Rio Kiev.
(MOD PROMINS) BLOOID-TRANSFUSION)

ALKI(SUEVA, .1.11. fiUsks!eieva, I.N.]
-- ...
al' a nIngle tramfuziun of a protein blood substitute (EiK-8)
I i
.. c ark, Blimac acra on blood serur proteins in Ue body.
Fi:l:ic,l. zhur. [uirr. 8 no.5:671-675 S-0 162. (MIRA 17:11)
1
.. laboratux-1,yu dlya lzuot~eniyR dk4yvt\'Iya bic>Ficheski aktivn)iLh
vcah~-, t3tv lnatJtjtA flz:ologli L*a. Rogoaxllt:ia AN UkrSSR, Kiyev.

Y11.A. sokukotrokyl, _7'0.0.]; AUILEYEVA, 1.11. [AlakeWeva,
'pa
FE[,Chmv:AYA,
Efriwl cf Intraveroue injerti,-Itw (.)I* L,'gh ,:Cne~i cf art',(,varial cytotaxic
sarmn tit, U-3 u")ua~ :, -je of w! .1te rnts, [Ukr' 9 no-3:393-
.yc j -
3-,)4 163. (1,-"RA 18:1)
2. Laboratorlya IzuL!!.v!-1'a .-Jiosk~ ull ~v institu'La
aj,! W,Corto' I Lou AN 11kr."'I"If, K-'v(:N .

IRZOIXFUK, To-4A,j AlAIN-13VA, I.P.
Ll WA, laid and their
"AorpA tuw of glycccc~
anions a Zbur. prlkl. kbimi,4no. lOz2390-2391
0 165* (MIRA 18:12)
1. lAnimLnA kly *atainskly institut Ineni I.?. Paylova.
sul"attoa MiLrob 23W65.

S/079/60/030/007/021/039/XX
P00l/B066
AUTEMRSt Ailskneyeva, I. P., Pesotskaya, V. M., and Ptitsyn, B. Y.
of Permanganate
TITLEs Oxidation Potentia ~1
PERIODICLU Zhurnal obsbehel khimii, 1960, Vol. 30, No. 7. pp. 2104-2108
TMMt The purpose of thin work was a more exact characterization of the
oxiaizing effect of parmanganate. Its oxidizing effect depends on the
acidity of tha solution, but research workers disagree in this respect.
The investigation of the dependence of the potential of the permanganate
solutiocn on p1l is of interest since the reduced form which is in equi-
librium with the permanganate ion may be determined from the potential
an a function of the percentual content. In an acid solution, the latter
may be in equilitrium with some of its reduction products, except ,.om-
pounds of bivaleot wmganese, as potassium permanganate oxidizes the Mn-
at any percentmal content, Thar fore, the universal equation
9 - 1510 + 52`1~ Ig [MnO4] [R*
5 n- --I
FM
Card lit,
I

Oxidation Potential of Permanganate 3/079/60/030/007/021/039/XX
BOW/SO66
cannot be used to characterize the oridation properties of permanganate.
To tudy these vtates of equilibrium different methods were applied
(Re;s' ~-5,6,7)-, D- V. Ptitsyn and V. F. Petrov (Ref. 8) indicated that
also In the case of bichromate solution the oxidation potential may be
affected by the nature of the acid. This might also apply to permanganate.
The pres-,ent pap*r deals with the following problems: 1) Quantitative de-
termtnation of the oxidation potential of the permanganate solution as
dependent on thtt pE of the medium. 2) The question as to whether the natum
of the acid influences the potential. 3) A more exact characterization of
the states of equilibrium established in the permanganate solutionunder
the conditicne of the experiments to be performed. The authors investi-
gated the olceendence of a potassium permamganate solution (0.01 mole) in
solutions or Hoo 4' H9030 11 2s0 40 CH3COOH. The affect depends on the
nature of the tocid at low pH only. An attempt was made to interpret the
nature of the roduced forms which are in equilibrium with the permanganate
ion, on the heels of the functions of the permanganate solution potential
on pH 4-n solutions or different acids. Table I gives the data of the
potqntlal dependence of KMnO 4 dissolved in HCIO 3' and Table 2 the values
Card --,/3

i-on Potelutial of Permanganate S/079/60/030/007/011/0391,'-Y~
B001/B066
AE/,A, pH I''or various redor systems. The diaerazi illustrates the oxidation
Potential of polass2um parmangimate as deperdent on pH in the presence of
different ncid.v. For the oxidation potential of permangarate in HCIO4 and
R103k 9 wan fcuiid. to be 1600 mv, in H2SO41 E - 1650 mv. There are
1 rigunt, 21 tables. and 9 references$ 4 Soviet, 4 US, and 1 Spanish.
ASSOCIATIONt Don.ingradskiy tekhnologichookiy inotitut pishchevoy V/
p.romyshlennosti (Leningrad Technological Institute of the
Alimentary Inilust v
SUBMITTEDr Ju.1y 6, 1959
Card ~13

ltzrsxyzvk I.V. --
Intra"sal ume of tincutre of aloe in atrophic namopharyugitis &nd
ozone, Test. oto-rin. 18 n0.1:22-24 J&-F '56. onaA 9:6)
1. Is kliniki bolean4W 14:ha, garla I nosa. (dir.-daystvitollnyy chlen
AN SM prof. B.8. Proobras bans k-Ly) lechabnogo f-,'Ullteta 11
Mookoirskago meditsinakogo Institute Imeni I.V. Stalinim.
(PRAMGITIS
naeopharMitiv, ther., aloe tincture)
(RHLKITIO. ATROPHIC, ther.
aloe tincture)
(RHUMS
wsopharyngitie, ther., aloe tinctura)
(ALW. ther. use
aloe tinoturm In atrophic rhinitis & nasopharMitim)

REZHIXOV, "L; SHAMASH, S.Taol ALEKSEMA, I.Vo
-t~.
State of students' krxwlodge in pb7oles. lPiz-v dhkOIG 21
no.4:506-53 Jl-AS 161e (KERA 14:10)
1. Se)cWr obuchomiya fisiko ingtitate, oL*hohego i politeUmicheskogo
obravoyodys. Akadeali podagogichookikh no4k RSF5R.
(Fv8ics--StUd7 WA teaehing)

SHAPCORMCNA, Z- 1R.1 ALUMMA, I. V.1 RCMSKry, I. R.
Mmtb*d of prowring purs lactuume vith the aid of ton exchange
r*sjW. Ukr. We. sbur. 28 no.63724-725 162.
(MM 15110)
x. rmptAtut organicbeskor kbim" AN ukrssR.
(L&ctuaces) (Ion exeMngs resins)

SUIWMIKCFVA, Z.B.; LISOYSMA, N.N.j ATXjSHXMtA,-~-; ROMMKII, I.R.
S~mtb*mes of tosyl ebters of lactose and lactulose. Ukr.khin.*iur.
28 tw.7:858460 162. (KERA 15:12)
I. ixptltut orgaincheakoy 101-11 AN Ukx6S&
(lactose) (Lactuldne) (Tolueneoulfonic acid)

IMINSM, X.R.; SHAPMMMOVA, Z.B.; LISOVSKArA, N.N.;
ALXKSK
.,W
-.0 .
Structure of toiryl derivatives or iactome and lactulose.
Ukr. kkiim. shur. 29 no.48420-423 163. (MIRA 16t6)
1. Inatitut oroanlebm koy khiuii AN UkrSSR.
NO-tom:) (Lactulose)
(Toluenesulfonic acid)

YV=MIY. A.A.. otv.red.; YAOUAVSZIT,, S.L.. nauchn" red.; SAMOVSKIT,
LV.. vsdushchly rod.; ALMSBIWA, X.A., red.; OADASKIKA, N.D.,
red.1 W20MITWA. X.Mov red.; KOBILIT. V.A..
rod.i MM, S.Z., red.; PMOMIT. V.V., red.; TIODOROTICH. V.P.,
red.1 SOMMOMIT. la.l., red.% G=MIYBYA, I.M.. takhn.red.
(Collection of reports of scientific research carried out between
1950 and 19571 Sbornik referstov nauchno-iseledovmtel'skikh
rmbo4, vnmlaenj%ykh v 1950-1937 rX,. Leningrad. Gos.nsuchno-tekhn.
ind-vo naft. i gornc~toplivnoi lit-ry, laningr.otd-nia, 1958.
158 P. (KIRA 12:9)
1. Tussoyumnyy mmuchno-lealedovatel'skly institut po pererabotke
neftl i poluchaniyu iskusetvannogo shidkogo topliva.
(Petroleum research)

AUTHOUSt Rudk:1vak-IT, D, 141i Trlf4,~.-L`, A. G. and -ks
TITIXt PrepanAtiCIh t.,I' Ce Aitc,41,-:1i fr~,n
ftel Fractiti;i,L 1!7"uhe 07,j--Sy~-.theals.
fspllrt5~, -( -
MIODICAM Khimlya
pp~ 17 24. (05SH).
ABSTRACT: TKe furA&zi;::ta'-, .~f tne a:-.i the
U11,4:9 of ~vl 9-~e ::,et lewell
thssa and
ara t:;X:~allent
pr..-)dtAct-I are h g-
f ictrat',cii a g i ~t;t 114.giit m-ta-- ar.~~ I'Lir 31ac-k-
,Rasult;B cf thq rroparat-1,:--i Cp_-Ce alde-
h*ydss frWri fuel fra-I.Icr-3 a v a g -
R r, . The Influer. e ~f the :.r.-.0ntratI..r L-f tn3 :;atalyit,
tKa Lhe s:--rthesIs
pas, the rate C~f 3U,~VIV Cf the l1quid raw ma-lerial amd of
the rate cf ~111:.,,fulat-lt-.,. -j' t~.a pa3 .;II Itht? :-artonylatiol'.
krc-:,tI,v3,W--,e The raw matqr:.a'. usqu wa3 the
fraction ilqj.~.zg ur t j !'DO T~h-',`- -mat., a
nirn luxlzW, two of oracke:1
petn,lcum. Va,~. p%yelcal
f t.-Is Yrao:ticln
Card 1/4 are 113ted as wel.L ax t',.-) Lt C-6 a!-,I 07 hydro-

!~ 7a, 5 - r 8 - 6 - 4/1-15
P reparation of go - G9 AlcoY--a Y'rzm 0jr.1--r-7 Put,', Fra-ticna
by the Oxe-Synthesis
carb.)ns In th.4 raw mat&rlal ~Table Tj-.0 3xp;arImentn
were 3a"W ~ut on a c,~ntinuous alparatus
Details of the process -f ~f unsatufatsi
h7dr.:,oarI-.,ns are Oct%alt was used as
catalyst. Mho --'rfIuei3a .f the -:,n-entration of this
oatalyst. on the rate of -,~f u.,isaturated
Cm - C7 h7drcoarton3 was ln.,astq-ateel at a temperature
0? JeZOG, pressures %~,f 200 and 380 at'ns and therratiz.
of the rat& ef supply to the reaw matertal was 3.6:1.
The %-oi~ame ,f gas = 0. 1-1- cf r a rt
material. The c.~,nc-siitrat:.cn zf tine -ataiyst wa3 zhanged
Withir tile i. 0.31%. Jesuits of these exj?eri-
ZlIts 0.03 ..
ments arg giver i-, Table --, and Details of ivresti-
gations -i-n tht 1rifluence -.f tamperature ~,-n the rate of
the reaeticr, at 2-)0 atts ari e,,-jFr. -n Tab.,,e 3 and Fig-3.
A-zt!-,ratior, erergy was a!valatel t.~ the equation
by Arrh;nius and Wa3 - il.000 Cal Tja temperature
coefficlent of the rate of rea:-~tizn -- -.4. Exleriments
on the effect z-f pzasaure the procens
we~-a 'ar-Iel ~ut at .'.IV I&FZIj3 ~f (rable 41
Card 2/4 and Fig.4.). W~nen tA* vras -azrlt-d --vut under

Preparatior (..If C - Aa .:c,~ f rom G-lef In -C,nt,~Aki-- j- ?ractIzvn3
by the 03co-syntLeals.
indu3trlal 'lame rate_ :~:-n_antratlcn
of he ~ata!Tz,:. a clanlre ~' n ti.~ frzm
f -31D-
150 .- 7,00 atms tLes nct, afrezt ti,i~ de; tli,3 -1 2,3!::e
5). lu: i~ zj ' I ga ti -., r the I----_ c a cf the ~Omvc-
tilt.1-4:n J thi-., gati ~:n tn:, Piccess w6re --arrIzId zmt at
varyinf; partlal CO &~-A 14.,- and
-f tne :-ws r~tr 3. Fr 11 at
la C'M I a
a-jj 1'_c.5 1~ ,-a.-. "-ve-j tj-,at at :.cw
renforatures :L40-. ','Ithe Lici; tl- ' ~I' ~