SCIENTIFIC ABSTRACT SABSAY, B..I. - SABURENKOV, P.A.

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• Collection: Scientific Abstracts
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• Document Creation Date: November 2, 2016
• Document Release Date: August 23, 2000
• Sequence Number: 7
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

SABSAY, B.I.
Changes in the spectrim of enzyme activity of the gastric; glands
following extensive resection of the small intesl,A-re in dogs.
Biul-.eksp.b,j.ol.i med. 57,no,.5%15-19 My 164.
(MIRA 18,'2)
1. Laboratariya, fiziologii i patologli p-Ishchevareniya (zav.
prof. S.I.Filippovich) Instituta normal.1noy i patologicheskoy
fizlologLl (dlr. - deystvitellnyy chlen AMN SSSR prof.,V,V.
Parin) AMN SISSR, Moskva. Submitt-nd February 12, 19614.

VOLKOVA, T.V.; SABSAY, B.I.
Effect of the properties of chyme on the secretory and notor
function of the gastrointestinal tract. Biul.eksp.biol..i red.
58 no.10-20-24 0 10'4- (14IML !8:12)
Iaboratoriya fiziologii i patologj~-Aishchevareniya (za%,.
y i patologicheskoy
.prof. S.I.Filippovich) Instituta normal no-
fiziologii (dir. - deystvitelInyy chlen AMIT SSSR prof. V.V.
Parin) AMN SSSR, Moskva. Submitted June 17~ 1.963.

SK85AY" AJ.

SABSAY: B.1,; KULIK, yu.ya.

I . "" ,
K OTIR A N K A Y A A. S. 4 S A H2AY . ". y 11 ~ ! f'.' " L, ~-, r -.-; 1, 1 1~ Z, h ..: i~ 1 'ra ~ 1'.'VV7~- -PU ~ Z~, vp.. ;

SADSHIII~'A, Ye. Yu.
USSR/Arledicine - Tubercul.osis, Diagnosis May/Jun 48
Medicine - 3putwn, Em-dnation of
11Clinical and Epidemio logical Significance of the Oligobacillary Condition," Prof I. I.
Berlin) S. i% Berguan, V. 5. Ioselevich, U. P. 11eleshkevich, Ye. Yu. Sabsh-ina, Ye. M.
,Nilova, M"oscow Oblast Sci Res Tuberculosis inst, 9 pp
"Proble-my Tuberkule-zall No 3
ieport extensive obsemrafLions on 108 oligobacillary cases. Studied gastric contents by float-
ing method. Method is of considerable importance in the differential and diagnostic analyses
of nonspecific and basic tubercular cases or those with accoripanying tubercular condition.
PA 7/49T69

USSR/Nuclear Physics Installations and.Instruments. C-2~
Methods of Measurement and Research.
Abs Jour Ref Zhur Fizika, No 4, 1957, 8517
Author Kalomenskiy, A.A., S
Inst
Title Passage Through Critical Energy in an Accelerator vith
Strong Focusing.
Orig Pub Zh. tekhn. fiziki, 1956, 26, No 3, 576-584.
Abstract As is known, thestabilit
.;yof radial-phase (synchrotron)
oscillations-in Accelerators with hard focusing is des-
troyed at a cei~tain energy, called critical, and depen-
ding on the structural parameters of the accelerator.
Analysis of the possibility of going through the criti-
ce~ point is essential for the theory of accelerators
with strong focusing. The authors have considered the
ofthe
equation of phase oscillations in the vicinity
.
critical point and the requirements that must be met
-when going through this critical point.
'Card' 1/1
-----------------------------
----------------------------------------------------------------------------------------------- ---------

J
1UPPHORS: Kotov, v.Il, and Sabsovich, L. L. 120-6-3/36
'i "-- L T LE Increasing the Beam-target Impac Time in Synchrotrons
and Synchrophasottirons (Uvelicheniye dlite__1'rj.3sti soudar-.
eniya puchka s mishen'yu v sinkhrotronakh _J sinkhr-ofazotr-
.onakh)
PERIODICAL: Pribory i Tekhnika Eksperimenta 1957, vo.6,
pp. 19 - 21 bSSR).
ABSTRACT: A new method of displacing the beam in the 250 MeV syn-
chrotron of the Ac.Sc. USSR is described. If one slowly
lowers the amplitude of the high-frequency, accelerating,
voltage, the region of,stability becomes smaller and the par-
ticles gradually depart from synchronism. These particles
do not on the average receive any energy from the accelerating
system and moving along spirals they impinge upon the target.
With such a mechanism of displacing the beam one can consid-
erably increase the duration of the beam-target interaction.
The duration of the pulse at the target depends on the rate
of fall of the amplitude of the HF, the smaller -the rate of
fall the longer theduration of the pulse. It is shown that
the only limitation on this effect is the momentum spread
introduced by the above procedure. The amplitude of the EF
is calculated subject to the condition that the particle flux
C~i a:,dl /2 at the target is constant. M.S. Rabinovich collaborated.

AUTHOR: _SA1KOVICH,_b.L. (Leningrad) PA 2224
TITLEt On the..Computation of a Determinant which is used in the Theory
OfMathieuis Equation. (Vychisleniye odnogo opredelitelya,
imushchego prilozheniye v teorii uravneniya Matlye. Russian)
PERIODICAL: Prikladnaia Matematika i Mekhanika, 1957,, Vol 21, Nr 1, PP 145
1522 (U-S-S.R-)
Received, 3 / 1957 Reviewed: 41 1957-
ABSTRACT: On the occasion of the solution of some problems connected with,
Mathieu's equation infinite determinants are to be computed.
When determining the characteristic number of Mathieu's equation
ytv + (,k- 2q cos 2x)y = 0, an infinite claterminant with the
following elements c.., which are different from zero are to be
ij '2
computed: c. 17 c c 4i
( (+O~. This determinant is usually computed for small q
on which occasion only terms of the order of magnitude q2 or qA
are computed.
Similar determinants are found when dealing with the problem of
the determination of the particular solution of an inhomogeneous
Mathieu..s.~equation with a periodic right side, the frequency.of:
which is a multiple of the frequency of the periodic coefficients.,
Semi-infinite determinants D occur in connection with the solution
of this problem.
Card 1/3

PA 2224
On the Computation of a Determinant which is used in the Theory
of Mathieu's Equation.
The present work replaces these semi-infinite.determin&4nts for
certain values of X and q by approximation by determinants*o f the
fourth or fifth order. In the case of the here assumed values.of
;L and q a satisfactory result is obtained considering the relative-
ly low degree of accuracy, but in the case of an increase of q
and a greater accuracy the minimum order of the determinants, to
be used increases.
Theauthor here describes a simple process for the computation,
of the semi-infinite determinant D with an arbitrary degree of
accuracy, and this process is suited also for any values Of q..
The-determinant 4(0) is expressed by the determinants D. The in
dividual chapters of the work deal with the following: Some
properties of the semi-infinite determinants D, evaluation of
certain occuring sums, two different methods of computatihg~the
determinants Dk at k -> oa, computation of the finite determinants
8
k
D,,.,application of the determinants D8for the computation of
the determinant L(O), determination of a particular periodic
Card 2/3 solution of Mathieu.'s equation with a right side the frequency

ACC NR: Pj,6024648 Monograph UR/
'Aynberg, Viktor Davidovich; Gavrilenko, Yevgeniy Timofeyevich; "a s
Leonidovich
Progrimming for "Ural"; "Ural-211 "Ural-311, and "Ural-411 electronic computers
(Programmirovaniye dlya elektronayk-h vychislitellnylth mashin tips. "Ural";
"Ural-2", "Ural-3", "Ural-4") Moscow, Izd-vo "Nauka", 1966. 367 p. biblio.,
tables. 20,000 copies printed.
Series note: Fiziko-matematicheskaya biblioteka inzhenera
TOPIC TAGS: digital computer, computer programming,
=R4:iag, automatic,
programming/ Ural-2 computer, ural-3 computer, Ural-4 computer
PURPOSE AND COVERAGE: This book is intended for persons using the Ural series of
computers. The book may be also used as a textbook on computerprogramming.
Command systems, programming methods and procedures for the Ural-,2, Ural-3jand
Ural-4 computers are~discussed, and description is given of the application of
these computers. Numerous exampleB of command application and programing
processes are presented,
TABLE OF CONTMIUS:
Foreword 7
1/2 UDC: 519-95
Card

SUBJEECT USSR PHYSICS CARD 2 PA 1424
AUTHOR ? 66ZRJAKOV,M,G.j 'T-zGUTOV,B.S,, VZORO_~.!.K-, Z?ELOT,V.P.,SABUDIN,A.F.
TITLE The Magnetic Analysis of the Reactions pp
Pp ppro (II)
pp -> du'~'(III) at an Energy of 660 MeV.
PERIODICAL Dokl.Akad.Nauk,109, fasc-3, 499-502 (1956)
Is sued: 9 / 1956 reviewed: 10 / 1950'
For the.purpose of the determination of further data concerning the character of
'the production processes of positive pions on the occasion of (p-p) collisions
the authors studied the momentum spectra and angular distributions of the se-
condary protons emitted on the occasion of the reactions I and II at 660 MeV.
Independent interest was caused by the possibility of separating (for thE pur-
pose of a subsequent determination of their degree of polarization) the deuterons
produced on the occasion of reaction III from the total flux of secondary par-
ticles., In connection with some further measurements such an experiment permits
a complete phenomenological analysis of rea ction III including the determination
of the ratio between the intensities of the two possible transition.,~
1s0 3si and 1D2 ---;; 3si, which correspond to the emission of mesons in the
p-state. The experiments were carried out with the 6--meter synchrocyclotron of
the Institute for Nuclear Problems ofthe Academy of Science of the USSR. The
energy of the protons was (660+31) MeV and the half width-of the proton spectrum.
was + 5 MeV. The scheme and the setting up of the spectrometer are then dis-
cuss;d.

Dokl.Akad.Nauk,10q, fasc-3, 499-502 (1956) CARD 2 / 2 PA - 1424
The relative momentum spectrum of the particles was measuxed by changing the
magnetic field strength. The effect on hydrogen was determined from the differ-
ence of the yields of polyethylene" and carbon targets. The momentum spectrum
of secondary protons and deuterons etermined thr3ug;i an angle of 70 is shown in
a diagram. The most intense peak at HQ = 4260.10 Gau3s.cm corresponds to 'the
protons elastically scattered on protons through an angle of 170 (in the center
of mass system- The peaks at HQ = 4520.103 and HQ - 2860. 103 Gauss cm correspond
to the deuterons of reaction III scattered under 430 and 153,50 (in the center of
mass system) respectively. The experimental and the computed location of the deu-1
tercn,peaks with respect to the peak of the elastically scattered protons differ,
by less than 1%.
The continuous spectrum belongs to the secondary protons of the reactions I and
Ii. its upper limit is in agreement with the com uted value (for the investigated
p
reactions 3560.1o3 and 3590-103 Gauss.cm respectively). The spectrum of the
secondary particles produced on the occasion of (p-p) collisions was also ob-
tained at an angle.of 12.21 towards the primary bundle. In this sase the deuteron
peaks were about HQ = 3220.103 and HQ = 395000-'~ Gauss.cm. The form of the momen-
tum spectrum of the secondary protons changes considerably with angular distri-
bution. The protons with more than 250 MeVe are emitted mainly towards the front
and the rear, but protonswith smaller momenta have a nearly isotropic distri-
bution.
INSTITUTION: Institute for Nuclear Problems of the Academy of Science in the USSR.

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-I -- ---ANDR I r'. P'. ,
SABUIN, L. A.j' LESNOV, -F S.,
L
~j;
"Polydiethylsiloxanne Liquids,! paper submitted at the Symposium on
Organic and Nonsilicate Silicon Chemistry on 12th-141-th P'"ay lc'58,
Dresden.
('rhe action of acids and aldehydes on diethyldietlioxysilane and its
mixtures with triethylethox-jsilane).
1. Reactions will be studied which take Dlace between d-iethyl-
diethoV,silane and its mixtures with triethylethoxys-ilane, and sulfur,
phosphorus, boron, monocarboxylic and dicarboxylic acids as well as
aldehydes.
2. Conditions will. be described under which liquid ethersiloxanes
or mixtures of polymers with functional groups are produced.
The chemical c osition and degree of polymerization of the
OMP
polyethylsiloxanes will be explored which depend closely on the
nature and concentration of the acid, the stoichiometric amounts
of the reactants present and the conditions of the reaction.
Abstract: B-3,108,944 (Encl.)

50) SOV/79-29-4-51/77
.AUTHORS: Leznov, N. S., Sabun, L. A., Andrianov, K. A.
TITLE: Polydiet hylsiloxane Liquids (Polidietilsiloksanovyye zhidkosti).
I.~ The Effect of Sulphuric Acid on Diethyldiethoxysilane and.
Its Mixtures With Triethylethoxysilane (I. Deystviye sernoy
kisloty na dietildietoksisilan i yego smesi s trietiletoks-i-
silanom)
PERIODICAL: Zhurnal obshchey khimii, 1959, Vol 29, Nr 4, pp 1270-1275
(USSR)
ABSTRACT: In the paper under review the authors give data concerning
their work during 1947 in the field of the preparation of.
liquid polydiethylsilo,xan.es from diethyldiethoxysilane and its
mixtures with triethylethoxysilane. It was the objective of
this work to synthesize polymeric liquids free from impurities
of those polymers which contain ethoxy groups in the molecule.,
The hydrolysis of diethyldiethoxysilan.e in an aqueous medium
at 1000 resulted in the formation of the dip-thyldioxy- and.
oxyethoxysilanes which, in turn, were transformed in 0
t pol.
diethy.1s,iloxanes of cyclic and normal structures- (Scheme I~.
Card 1/3 Under different conditions the formation of:polymers containing

SOV/79-29-4-51//77
Polydiethylsiloxane L-iqt,,,ids. I. The Effect of Sulphuric Acid on Diethyldi-
ethoxysilane and !ts Mixtures With Triethylethoxysi lane
the ethoxy group (b) in the molecule could not be avoided. The
synthesis of polydiethylsiloxanes free from ethoxy groups on
the basis of the hydrolysis products of.diethyldiethoxy-il.arie
was carried out by means of a reactio n with 93-100% Sulphuric
acid at 20-500 as well as with 95-99% formic- or acetic acid:
at 60-1000 according to scheme (H)..When sulphuric acid.w1as
used 'the fractional composition of polydiethylsiloxanes changed
abruptly toward the formation-of. polymers of a higher average
moledular weight (Scheme III). The carboxylic acids did not
cause a regrouping of the cyclic polymers (Scheme II, Table 1).
On the basis of what has been reported so far it was possible
to assume that the synthesis of,polydiethylsiloxanes free from
polymeric impurities containing ethoxy groups in the molecule.
by the action of concentrated acids (esp. sulphuric acid),. 11
upon diethyldiethoxysilane follow's the general scheme (IV)
(C H 2 H SO H + 2C H OSO H
2 5)2S' (OC2H5)2 +. 21 4 I(C2.5)2S'O]Y- 2 5 3
+-H20 (IV) . TIhis ag'sumption was confirmed by experiments.:Thus,
ethyl sulp4uric acid and cyclic polydiethylsiloxanesf-ree from
Card 2/3 normal polymers with ethoxy groups in the molecule were ob-1

SOV/79-29-4-51/77
Polydiethylsiloxane Liquids. I. The Effect of Sulphuric Acild on Diethyldi-
ethoxysilane and Its Mixtures With Triethylethoxysilane
tained (98% yield). The investigation of the influence of
various factors upon the process and composition of the result-
ing polydiethylsiloxanes made it possible to illustrate -the
main transformations in the schemes (V), (VI), (VII), and (Ix),~,
es.
vhich was also confirmed experimentally. There are 4 tabl
SUBMITTED: March 10, 1958
Card 3/3
L

5 (3)
A*UTHORS: Leznov, N. S., Sabun, L. A., SOV/79-29-4-52/77
Andriano
v, K. A
TITLE: Polydiethylsiloxane Liquids (Polidietilbiloksanovyye zhidkosti).
II.The Effect of Phosphoric- and Boric Acid on Diethy1diethoxy-,
silane and Its Mixtures With Triethylethoxysilane (II.Deystviye
fosfornoy i bornoy kislot na.dietildietoksisilan i yego smesi s
trietiletoksisilanom)
PERIODICAL: Zhurnal obshchey khimii, 1959, Vol 29, Nr 4, PP 1276 1281
(USSR)
ABSTRACT: In continuation of the preceding.paper (ZOC 1959,29,1270) the
data concerning the reactions of phosphoric- and boric acid
with.ethylethoxysilanes are described in the present article..
It was shown that, like sulphuric acid, phosphoric acid react-
ing with diethyldiethoxysilane results in a formation of poly-,
diethylsiloxanes free from impurities of normal polymers with
ethoxy groups in the molecule, and in the formation of acid,
ethyl phosphates. This formation is brought about at a molar
ratio of diethyldiethoxysilane to the acid of 3:2 up to 1:2.
There was no neutral eater to be found in the. reaction products.
~.Card 1/3 In contrast with the reaction of diethyldiethoxysilane,.w.ith

Polydiethylsiloxane Liquids. II.The Effect of Phosphoric- SOV/79-29-4-52/77:
and Boric Acid on Diethyldiethoxysilane and Its Mixtures
With Triethylethoxysilane
sulphuric acid (Scheme 1) the reaction with~phosphorio ao id ex-
hibits an intermediate stage in whicli.polydiethylailoxane phos-
phates form, Which are stable in the middle of thetreaction ac-
cording to scheme (II). if water influences the reaction pro-,,
duct, a hydrolysis of the phosphates accompanied by the separa-
tion of polydiethylsiloxanes and acid ethyl phosphates takes
place according to schemes (III)~and (IV). It proved impossible
to remove the polydiethylsiloxane phosphates since the distil-
lation of the reaction material resulted intheir decomposition.
Their presence was proved in three ways. The date obtained sup-
port the assumption that two kinds of polydiethylsiloxane phos-
phates are present in the reaction product (Scheme II). In the
hydrolysis (Scheme III) it may be seen that polydiethylsiloxane
~phosphates exhibit a polymeric.grouping as soon as the acid
ethyl phosphate is split off. A further condensation results in
non-distillable polymers of high molecular weight. In this hy-,
drolysis (Scheme IV) individual polymer components, the cycli-,
zation of which results in low-boiling products, liberate them-
Card 2/3 selves. The effect of phosphoric acid on a mixture of die.thyl-

Polydiethylsiloxane Liquids. II.The Effect of SOV/79-29-4-52/77
Phosphoric- and Boric Acid on Diethyldiethoxys-ilane
and Its Mixtures With Triethylethoxysilane
diethoxysilane and triethylethoxysilane follows scheme (V), as.:
is also.the case with sulphuric acid. The reaction with boric
acid in place of phosphoric acid takes place in the same way
(Schemes VIII.and IX). The fractional compositions of the poly-
mers obtained by the reactions of both acids are similar. The*re
are 3 tables.
SUBMITTED: March 10, 1956
Card 3/13

't` V~: C R Lezacv, S. 3nb-n, L. A.

TIT!;.;,:
uil- Pol id i e ti i 1. o',,--,;n
2t'r 1-s_llo:~anc Lif,
__Qvyy e
,
35. Effect of Car-~-:,-,~ylic Acids _;!~f)n Oictz-lyl-
e s i 1 ane ("i. Deystviye kn.rlbonovykh kinlal r1l

'~',hurn-~l obshobey khi Vol 29, '~;r 5,
miL, 19599

rlreniz-t pr~ier supT)liez date. of the re-,3ctiono of eir-_thyl-
The
jiethoxy-silane with monc-.(Table 2) and dicnrlboi~ylic.vcid,s
(TtOble 'p). Tho lnvestilg~~ticn Iof these renctions indicrted:,
thant on heatinj cf mono carboxyl -i c acido kformic, acetic, chloro-
~ceticl propionic and n-butyric acid) vith die thyl-dic, thoxy-
silane uvp to 66-1200 polydi-ethyl-silox,3nes Oap to ~9 ~~,l and
ethyl esters of the corre;3ponding acids (Up t'q -.,c P-re
formed. Cyclic polydiethyl-silcmanes, -.-Ithout lirlear Polymers
with ethoxy-groups in the molecule can 'the ~obtained it excess
acid ir, used in -the reaction. The latte'r depenrla vri the acid
concentration nnd. it-, dissoci-,tion const,-nt ~.re iacreaaas
Card I vrith ~~n increase in the 1 a t a r Tnb 1 a I Tne re,~.ction rate

2 0
o 1 r l' 0 1 c x; n e L i q u i -1 C 0 f
A-ids U-oon Die t-,yl-etho-x,,f-sil -Ine
11 no a On ds
o f 0 rb o;, ~~,rl i c i d o v, I t h
an sfrengtll of the acid r!'zvi inc-m7neo -.,iith ;~ts i ?I C ~~e 3 1 r, gr
_1,1
'I o
-
et Ll"ne
Off 'Ll. -0 GG -p
Their
fr!-, c t 6 na I cc-:,-positiori in cont..-;v,~ t' t',, ~a
!1C.4 U.::r -11 1 n:'~t "I "IC r( C, "I
t i
-a
z Or -IMCi-tz -tia if the -ac4d. T~
f
c t e d
c SU
!,-1 no -z- -~."P.Y'
e -:7 i 'b 1 i nrboxylic in a
lic acids t~-%lc
.-Irno"arDoxy
id o - ll:~ z- - t--o course of reaction ?;-n~l th't'
e (3 C i. C).n 3 f t. I ~acid desirable for o of
Th-- fractionial comno~At,:~-i nf ta
is si:ailer to the co;-apositinvnof those,
I C a f o v: k o,-7 -in Cll--~ reaction ~..,ith a-i -Is
anft -J,; -.3-co 4-n.-Tepenf!ent of the nature, of the acid i t may be

C P'3: Leznolr, S. , Spbun, L. A. Andrianov, GOV/79-29-5-24/75'
K ~P-

T -Iol,-!d.4eth-rl-silox:Ane Liquids
fpolidietilsilot.,sp-novyye
zhidi---ont-4). 4. riffect. of Aldehydes and Acetone on D4-C-,.hyl-
dietho3cv-silcxane (4, Deystviye alldel-idov i atuse-Lona na
dictil3letoksisilan)
PF7,10DICAL: Zhurnal obs4c'ey khiviii, 1959, Vol 2Q, "Ir 51
Pr
A3 TR C T Th-d authorr; found thrrt on the interaction of diethyl-dietho--y-
silane .-.ith aqueous aldehyde solutions.the lr-_tter e--o not take
th
j7irt ii c. --euction and that the process results ih the Ii7p~rol,-)-sis
of the die'~-.hjl-dietho-.cy-sil,,:zle. 'Mhydrotis aldehydes andlace-b6-10
are ccmpletely pas3ive in the absence of. catalysts with
respect to diethyl-diethoxy-silane. IrresDective of the tuime
of heating of the recction. mixture neither Polydiethyl
siloxanes nor acetals could be detected in the reaction
proe u
lucts. Jhen sing mineral acids hydrochloride and its,
solutions wore not found to cpuse~,?.ny,,in~uerac!~lion.bety~een
.--Idehydes and diet'nyl-diethoxy-3ilane.~Sulfuric -cid, aoweve-
C -~-rd 1/3 effi3Ct3 in "'-'!ftCunt3 of 0.1-0.2 cifo the form.ation of poly-ain-thyll

10
Unluids. 4. C-Lfect, o-f VP
0 :~-20 -24/75
Aldc'.yales mv~',, "cotone r~ri Die'u-hyl-dietl-oxy---ilox,-Lne
sila-can~io arid corresnondin- ncetals. In the investiration OIL
the reaction of diethyl-diethoxy-silane ~,.,ith for!-.,ialdeh,-Tde
(paraform).a prolon-ed time of henting vias fou-id.to cause tl,e
formation of a polydi6t',yl-silomane mixture with -- higher.
content of ethoxyl group7,3y the influence of dic1V-Yl formall
and alcohol upon -)olycycl.ic polydiethyl-oiloxanes treated -~,i i tu h
-L-furic acid a polydiethyl-siloxane mixture with 5-4 !o'
ethoxyl groups mr?s obtained. Acetone and diethyl-diethoxy-
silane reacted in t,-e presence of sulfuric ac-id traces and.a ,
polydiethyl-silo-cane i.-iixture formecl. Ket.91, ho7ever, -.,ms
not found in the reaction products. In addition to
polydiethyl-silo-kanes the reaction product contained alcohol
anda considerable quantity~of soluble resins which were
formed o7fin,!T to the condensation of acetone and probably
also of Since these resinsare dissolved b.-,, solvents
such-as polydiethyl-siloxane they could not be isol-a-Led. The
distillation in vacuura accompanied by deconiposition.
'Table 1 - interaction of dieth.vi-ethoxy-silane with paraform.,!,
table 2 - the sam.e with paraldellyde. There are 2 tables
C a

Polydlct'iyl-~7,iloxane Liquids. 4. Effect of Aldehyies SOV/70-29-r;-2k,-/75

5, (3)
THC p 73 Leznor, 3.1, SOV/79-29-5-25/75
S
I.ndriancor, K.
IT ME: Polydiethyl-siloxane Liquids (Polidietilsiloksanovrfe
zh i dk o s t i On the Reaction Ylechan-isri of Diethyl-diethoxy-
silpme --."i'.h Acetic Acid (K voprosu o me~-hnnizne realktz;ii
dietildicto'csisilana 6 uksusnoy kislotoyl
Zhurna.1 obahchey kh-iciii, 1959, Vol 20., -'r 5,
PP 1518-1522 (USIR)
A j T R,~ CT
reaction of' I,etli-,t,l-dic-t~lioxy-siln-ne
On investigation of the
with acetic acid 4t was -found that the elimini " ion of the
ethyl. r,.cet-a-te being formed from the re,-~ctiioa mi~,toure
considerably reduces the rate of the reae'lion in
connection the reaction -3roduct is enriched by polydie-.4hyl-
silo~zanes with. linear polymers ha7,,r-Ln-- e`-hoxi, llrou:~S c__L
ends. of. the -olecalar ch,-in.,In order to define t-he c:,enis-ri
of th-~ initial state of the reao,tion, e".erizents in toluene
%le(Uu.n. on continuous distillation of volati!-~ rerction
product3 were carried out. Polydiethyl-pilocaner. '.,.~~nd eth-,rl'..
ace tatr-. --were no
t .
found to be f ormed. Di
Cn-rd l
.
and the unchanged di ethyl -d ie thoxy-s.ilane -.,,ere found in the

Liqvid,!3-~ 5. On the Reaction
1, Acc-tic Acid
rpaction riroducts. The free ~11cohol waz da'ecte~! vn~
cond-ensate. Further reactions of
zrere investi~atod. It
theft by '10-ating of mc-thyl, ethyl and n-ljui7rl ni-ccl A .1
rtce to-m-y-s i lane the correspon(lin- c~ r, -1';,r t C. snr
,),l,fd-etn.yl-si1oxP-ne ~zdxtures were fo-riZc.,.. !n n.7~
nee
st~lfuric ricid +'-t~. !a-*-er
11 U.
tomou--nature. The chonict~l co.~i-)ositicn of Po
--ne~ in addition to cyclic oolyne,7~: -1zo
-pcly,.,,~ars with alkoxyl Croupo up to the ene, aton's-of
'e,
Leon. of clicthyl-dioxy-silane ir, r;3-ulIz-,
In a c:)T-.-oletc- el'imination,of water with po-,-. - tAyl-
silo~-,-vncs being formed. The chemical F-nalysia the
physical constrilts of the latter are indic;~tive o,L
Cyclic struetu--re. He,,,.tinp of diethyl-dio.-.-y-r-i1,--.no i-
-1, r, a
nhydr^11
-'cohol yields a poly.,ieric nix,ture in -..,hich l-in--Pr
poly:,,iers i ti, etho- roups uere detected. The nmo-.-nt of
xyl U
these -roups iz Jetermined by the acidity -of. t;He 0; n
dehyir;FLtion of diethyl-dioxy-silane in aalcolh,ol txac-s, of
Card sulfuric and acetic acid 3.58 and 5.47 ethiic-vi roup-:3 e r e

ilo.. 5. On ti-e Reac-L io S 0 V -2: -"-27)
n
r, r i o t -el L,~- tTlO:cy_ c; i lane t h,',cotic Acid
fc!.11-1 DI Vas ~Ibso-_,ace of th e s eacids their s not
-,n p xp -at v ~vvt -tveti, n
ml, ~n c n.
a
tllc~ -)-osence of rat", I Sulflu"ic -::r sulfuvi_~.
nnO c'uhyl P. c c c
C 4- S
Of
T-11cre p r L,

J'J~_T -70S -
Shteynber
, L~. Sabun, L. B4 7
,
,'
12 T 17 E The Relaxation of the Tencion at the Graill Boundary of
Alloyed Ferrite (Relahsatsiya napryazhenil'ya .c,
zeren leoirovanno[;o ferrita)
Ti T, I y y d o 11 -a 0. y v s s` e y s h k, o I y Le t 11 r y a ,
p.) 2o~f 214
th
~ors invezti~~atcd wh,ich way alloyed 1(?-.en-
t'.in process of the relaxation of 'the -'-- c -.1 Z i o
e ,,-Sin boundary of a-iron. The --lloyi-n,- of
lcrrir.e icads to t~-c increase of the activation c-,1z'_-y~
t G.~ `e -t
tly alloyed elenents have a differer.

on enarzy, T-4c- folioluin'~ eicmc~:~'ts Z:'I'~
accordinz to their effect on the act I v z. 7c 41' o n
en F_ rf~y. Cc~. Si, Cr, '.-o, The activat-ion enerL~y -!so
L'er'
nflucnced by copper., aluminium and tungst
-y
not by TII'ie higrlties~t values for the activation ener,.

C r I i'3 .
ained i7ith alloys of feri-ite with tun sten, sii~cori
were obt u

Tlte Relaxation of the Ten..:ior at t'.'.Ie Gr.-ain Bolan-dary S OV/ 1 3 - 3
of AlloycO Fer rite
'01, W r 'i
and ma n ~-a n ~I z-, eit0 of -At", chrOM-
and nan,~a:. s -.2 -":!!U-.
of the intern, "I ction 'ound rh-4cil -S
40-900 below, the -~axkaum of the i-ternal frictiG,
A previous purification of tile -Aloys from C, I,
as annealin.- of thie allor in hydro-en and in
I
do,~s, haviever, not- remove the new na-ximuLn A. TLIC
occurrence of the maximum cf internal friction io c-::-
ziai-n-d b~, the diffusion of .~'n Cr. An a~ldit-io,,Ll-
-,Ilcying t;,ith molybdenum conriletely removes the o c c u-- 0
of tide maximum as .,.,ell as "he internal friction A and
decreases theactivation energy at the &r--in bou--,(I-rj -
The i.rfluence- of --iolybdenum on ti-,e
of the ,maximum of the internal friction A is. ca,,:zod by
t lie infl=;ce o' t',lis met-al on the d4stributio-n o- Cr
L
--d I
in the a-colid solution. There are 5 --x re
e, and C, r-.-f--.rences, A of vthich are Soviet,
A 3-SC C 1IC':.' -pr.A-itekhnicheski-j institiitu
(Ural
Card 213 !:Is~---itute)

33463
S/129/62/00o/pol/oo6/oil
.Influence of thermomechani cal E073/E483
Deformation temperature , OC Increase-..(or-. de-6x-ease.). in
service life, %
197 -8
170 -12
228 8
228 8
229 8
228 8
251 20

The curve illustrating the .relationship between the service life
of'a cutting edge andthe degree of plastic deformation given.to
steel during thermomechani cal treatment has a maximuml for'the,
deformation range studied, the highest service life of the cutting
edge was obtained.in the.c ase of 15% reduction. Thermomechanical
treatment does not appreci ably influence hot hardness. The
increased service life was attributed to increased wear-resistance
Card 3/4

33463
S/129/62/000/001/006/01111
Influence of thermomechanical ... E073/E483
of the cutting edge; this increase was.most pronounced when
cutting materials of high hardness; practically no increase In
service life was observed in machining austenitic steels. The
thermomechanical treatment improved appreciably toughness of steel
in static be.nd.ing, it also 'brought about.refinement of the
martensite grain and formation of a texture. Magnetomet:eic tests
have shown that on increasing the reduction from 5 to 20- 30%,
the martenslt�c po:Lnt for the residual austenite during.tempering
is depressed 20 to 300C below that for undeformed steel. The
thermomechanical treatment had little influence on-the completeness',
of the transformation of the residual.austenite during tempering..
There are 5 figures, 4 tables and..9 references: 7 Soviet-bloc and
2 non-Soviet-bloc. The two references to English language
publications read as follows: Ref.l: D.J.Schmatz, J.-C.Shyne,
V,F.Zackay. Metal Progress, v.76, no.3 , 1959;
Ref.8; R.F.Harvey. Steel, v.147, 196o.
ASSOCIATION: Urallskiy politekhnicheskiy institut
(Ural Polytechnical, Institute)
Uralmashzavod
Card 4/4

., . ~'; a w . . . . -
~ -7111 - - -!~ ", -~ ca

b erm
_~wi thout the. a.,8ve: men,
cooled:to'00. C..and h6ld-,-,
up : to'-~,'
~320% h
ns which would pbrmit'.incre
~In ermed ate
20% Higher or;.Iower t
.-cuttij4'g,.pr.op,*e-A ies ,bu
re:-.thezv_.used ',;for-,maki
e ~.-was ~:comvarcd,,- with*,,..'a
ppera
hii` :-than th
r
6t
ing*.the,,cu
od Ing',temp
ii~m ..'a 1 g s d er

+

YASILITET, Y.M.; AVILOV, A.A.; AIMAZOV, A.D.; BALASHOY, A.Y.; YOLKOV,.A.M.;

~.-Cjy,namic: compoin
mom nt-,w ej
.~-canVcktei-Wit 4
--- ~7 4~ j~
1 h i htt ci
at- rii ay,ut~t er g -mon
ll~g
h LAZ'69v-crane resulted'in.re uc g.- 6--ove
K

24(o),
5(4)1 6(2) PHASE I BOOK EXPL401TATION SOV/2215
Veasoyuznyy nauchno-lasledoVatellakly In5titut metrologil Iment
D.I. Manduleyeva.
Referaty nouchno-Inaledovatel'skikh robot; aborn1k No.2 (Scientific
Research Abstracts: Collection of Articles, Hr 2) Moscow,
3tandartglz, 1958. 139 p. 1,000 copies printed.

Additional Sponsoring Agency: USSR. Komitat atandartov, mer.l.
lzmeritel'llykh priborov,
Ed. I S. V. Hashetina, Tech. Ed. ; M. A, Kondrattyeva.
PURPOSE: These reports are Intended for sclentists~ researchers,
and engineers engaged In developing standards, measures,
gageo for the various Industries.
COVERADEs The volum& contains 128 reports on standards or measure-
ment and control. Thu reports were prepared by scientists or
Ina It, Izater.,
t utes or the Komizet atandartov, mar I I ce2lnykh
priborov pri Sovato MInlat rov SSSR (Commission on Standards,
Measures.
and Ma4murIng Instruments under the USSR Council or
XInI2t0r. . The Participating 1natl4utas are: VNIIM -
)
Vassoyuznyy nauchno-laeledovatel,ekly metrologil imeniLD.J.
Mendeleyeva. (All-UnIon Scientific Research Institute or Mtt-
rology ImtnI D. 1. -Mond. leycv)
An Leninpradi Sverdlovak brancn,
or this Inatitmte., VNIIK - anoyuzMY7 nauchno-lasledovalell3kI7
V
instItut Kom1tvLA standartov, mar I I =erltel1nykh priporov
(All-Union Scientific Research Institute or the Commlasion
on Standards, Moazureg, and Measuring Instruments), creavd
from MGIKIP - Moakovskiy go3udarmtvennyy tnatitut mar I
Izm6rItel1nykh prIborov (Moscow State Institute or Measures
and Measuring Instruments) October 1, 1955; V"IIP7RI
Vo
noyuznyy nauchno-laol
dovatel-akiy Inatitut
flziko-tekhni-
:
:
ti
ch ski kh I radlatekhnich ak1kh 1--aldrenly (Ali- nion ScientifIc
R"aaaroh Institute or, Phy3lco technical and Radio-anginee.-Ing
Measure a ) In Modcow; KhGIMIP - Khar(kovdkiy go3udarstvennyy
T nt4
Inatitut mar I lzmaritallnykh PrIborov (Khar-kov State InatItute
of "assures and MaaaurIn&
In5tru;n
nta); and NGNIP - Novoal-
A
birokly goaudaratvanyy In ti tut m r I=er1ze11nykh priboroy
:
(Hovonibirok State Inatitute or Measures and Measuring InBtru-
m!&Qt,q), No personalities are mencLoned, There are no references.
of Conventiona I
(W(IrM). On the Accurac Cali-
bratioRa or Colorimatils).for Three Colors And Four Chromaticitit-3 10
Yustova' Ye. N. (VNIIM). Studying Spatial Variation or color
Perception Under the errect of Eye Adaption ill
Saburenkov, A.M. Measuring Variable Values qr Light 112
3aburenkov, A.M. (VNTIM), Light Measurements for Pluoreacent
Lampa 113
?Ilya loochemic 41 Mcanurementa (Romanova, M.P., Editort Professor)
(Sverdlovak.Branon of VNIIM). Designing A Potentio-
m~!;Hc Apparatus for Measuring pit lis
Alakallijorov.-N-A., Yi
rova (SveN.
_V._ShQ,1tWpaIbvA, and Z.H...Sun

"
IdVdW Firfinch of VNIIN . De lopIng a QuantitAt1va fiotolorlmet-!c
g
)
Micromethod for the DeternIn
ation or Phosphorus and Mangetnellt In
Cast Iron and Stool 116
C. a- 22/27