SCIENTIFIC ABSTRACT MATVEYEV, I.B. - MATVEYEV, K.I.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R032932930003-7
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: June 14, 2000
• Sequence Number: 3
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

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MOVE M P I.B., kand. tekhn. nauk
Selecting the type of drive for a machine for rapid forming.
(Nauch. trudy] ENIKWha 8t5"2 064, (KMA 180)

ACC NR.
AP602:Ld-c- b
SOURCE CM'6_UR764T3P 7,000/611&4616146
IIMNTURS: 14atveyev, Matvayevao M. N.
GRG: none
iTITLE: A hydraulic inertial vibropress. Class 58, No. 183070
SOURGS: lzt,breteniya, promyshlennyye obrazts;,, tovarnyye znaki, no. 12, 1966., 10
TOP-"G TAGS: hydraulic equipment, motal press, forge press, atetal forming press
ABSTRACT: This Author Certificate presonts z- hydraulic inertial vibropress contai
a base in the form of a closed power frame, and cylinders mounted in the frame arid
carrying'moivable working plungers (see fig. i). -To improve the efficiency of the
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press, a movable cylinder is hfuld in the base. This cyl-Inder contains an auxiliary
hollow which holds a shaft rigidly fixed to the base. The working plunger is
provided with collars through which power i's transmitted from the cylinder '.o the
product. Orig. r-rt. hast. I kigure,
SILA CODE: 13/ SUBM DATE: 03Jun64

NATVEYZ?, l.G.; RCIZINAj D.Sh.
Bensylamine (Q-aminotoluene). ?btod.poluch.khim.reak.i prepar.
no.4/5-.33-37 162. (MIRA 17:4)
1. Voesoyuanyy nauchno-issledovatellskiy institut khimicheskikh
reaktivov I osobo chistykh khinicheakikh veshchestv.

n AXOT, Sargey Nikolayevich; XffU7U, kandekhImenaukv otv. red.
Edecessed]; Clumov, rownw;vArawmamm. N.A.,
tokhzi.red.
[PolyvWl alcohol and Its derivatives) Pollyinilovyl spirt
I ej;o prolsvodup. Moskva. Izd-vo Almd.nank GM. Tol.2.
1960. 866 p, (MIRA 14:1)
(TIzWl alcohol)

POGORZLYY~ A.D.; M"alIDO, N.M.; HAVEEEV, I.I.
Regularities in the performanc-e of multi-Compartment, flotation
machines. Izv. vys. uchalb. zzv.; tsvot* wto J+ no*6*.16-
25 161. (MM 24 -12 )
1. Severokavkazekiy gornometbalurgicheskiy izatitut, kafedra
obahchey meta-Uurgii.
(Flotation-Equipmerit and supplies)

MATUM 1 1010 s go7m incho
Comparloon of tb a performace of rake-type and sp ral cUssifiers
at the Kirowsk# om-dresoing plant. Cor. sburs so*704-75
Ji 161, (MIRK 15:2)
le Sevwo4ULvka*mkiy gorno-votallurgiaboWdy inmVtutp g.
OrdshoaWdses
(Ore droissirgrArquipwnt and supp:Ljos)

MATYEM, I.I.
Scientific and Methodological Conforence on the elininstion of air
pollution. Ixv. vys. ucheb. sav.; tevet. mt. 5 no.4tlSS-190
062,, (XIRA 16.- 5)
(Air-Pollution)

MATVgmVY--.IOx,.q 'Ushe
Trial of the yacht "Antarctica.' Sudostroenie 29 nO.U240-42
F 063, (KMA 16t 12)

MA r~IW, 1. 1.
Some data on the influence of the wear of the impeller of
f1otation machines on its characteristics. Isv. vy's. ucheb.
sav.; tsvet. met. 7 no.5t29-33 t64 (MMA Igtl)
Kafedra, obogaehaheniya poleznykh iskopayemykh Severckavkazskogo
gornometaUurgicheakogo instituta.
JA

4144 :14ATUM X.10.
''I the grlp-ding-
cyalo.,.~ rSv6t&-M*t*-- 34 n0*-'A.t54 Mr 065o
(KRA 18t6)

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AUIRORs
PIRIODICALs
i
Card
Natveyev, I. I.
SOV/T2-59-12-2/19
Investigation of Surface Phenomena in Caloinable Porcelain
Bodies
Bt0k10 I ksramika, 1959, Nr 12, PP 4 - 7 (USSR)
In calcining porcelain the int,sra-41,jointing surfaces disappear
and the energy ionneot*d with theprocess In transformed. An
essential part of freed energy iq,..,%1kilised for the mechanic
p7octme of the approach of Individual particles and the filling
of pores as well as condensation of th* body. Part of the
nergy passes into mechanic work is-already proven by the
:
uthor in a previous paper Oaf 06, rhe Idealised scheme of
the interaction process between tvo' particlas in the porous
body in represented In figure.-I. The true poro:l;in 0 todi*8
have a porosity of about 40% cn calcizing up t 00 . On a
further rige of temperature the ooodozastion process occurs
under complicated conditions. In order to solve the problem
connected with the deformation of porcelain bodies during
calcination it in necessary to know the aospositions of the
liquid phase at various temperatures and their wetting abilitj.

Investigation of Surface Phenomena in Calcizable BOT./72-59-12-2/19
Porcelain Bodies
In accordance with expezineets by A. S. Berkman and
1. K. Natveyev (Ref 2) a considerable quantity of the liauid
phase form in the usual porcelain bodies already at 950 - This
fact may be explained by the presence of iron-, calciwii- and
other metal oxides in the raw materials of porcelain bodies.
Considering the contraction process by the action of surface
forces two subsequent stages in this prooe:s,aro pointed out,
i.e. thop at t*ap*ratur* intervals of fro 00-950 and
950-1200 . It Is of great intorest to clarify the chemical
composilion of glass which for--a at a temperature interval of
900-950 as vull as the adhesion of the cryatalline component.
Figure 2 shown the soheme and figure 3 the total view of the
systen used for such Investigations. Suba*qu*ntly the investig-
ation method In described. In figures 4 and 5-photographs of
nephelite g;ass on feldspar plates aro shown obtained at
900 and 950 . In the second stage of the process an approach
of the solid particles under the action of surfaos forces
takes place at a temperature interval of 950-1200 . In figure 6
the deformation curve for a given body is plotted at this
Card 2/3 temperature interval. The surface phenomena exert a considerable

Investigation of Surface Phenomena in Calcinable SOT/T2-59-12-2/19
Porcelain Bodies
influence on the process of body forsation by calcination. By
their Investigation valuable data nay be gained for the v-101
calcination process. ?her* are 6 figures ant 3 ref*rences,
2 of vhich are Soviet.
Card 3/3

BUDIKO, A.V.; BOGDANOV, G.I.; LEVITSIKIY, D.Z.; DROBOT, A.S.; YAKMNKO, K.F.;
MARCHMO, A.A~,-_JAnTYLMI I.Kj LEONOV, B.A.; BAECNKO, V.T.
Pillar recovery In the 7rivoy Rog Basin. Gor. zhur. no.5r22-21,
)V 165o Wn is, 5)
1. Institut gornogo dela im. A.A.Skochinakogo, Moskva (for Budlko,
Bogdanov). 2. Trest Leninruda (for Levitskiy). 3. Ruditik imani
R. Lpikssm7ourg (for all except Bud1kO, Bogdanov, Levitskiy).

- MATMEV, 1. L.
Alfalfa
Our exForience In raising alfall'a seed. Yorm. bteaa. 2 1kc. 1', 11,,52.
Monthly List of husaian Accessions, LiLrury of' ConEress, Nay 195.'i, UNCLA-'-b-:,1F1,!~,.

MATVZM# I*M-*; -GAIAMAGA# Z.H.
Perfe-it the tochniqu" Of h7dranlic fracturing. rieft. j:hOz.
38 noo9:15-17 3 160. (MIRA 13:9)
(Oil wOlls--Fqdraulic fracturing)

HATVM.NP I.M.
Effect of the numbor cf production wells on oil recovery. Geol.
nefti i gaza 5 no. 3t24-28 Mr 161. (,z-LIRA 14-4)
-r -
1. Neftepromplovoye upra7leniye Malgobekneftl.
(Oil fields-Production methods)
.I-

lem.
Exploratlon of sand preducers. Neft. khoz. 39 no.6:54-56 Je 161.
(MM 1i,: 8)
(Sand)
~-Ii
I

MiTaYlKV, I.M.
ChmqMs to the productivity of oil v0s during their developmant.
Weft. khos. 40 no.8s37-42 Ag #62. (MMI l7s2)

KUVEIEVj I.M.
Determination of the compre3sibility factor of fractured carb)n-
ate reservoire based o7a field data. Nefteprom. del* no-3:3-9
163. (NIRk 16:9)
1. Nefteproqvslovoye upravlenlya "ISM1gobaknefts".

MATVF-fF.V, I . M.
-4
Certain problems in the determinatlcn of boll-tca-hole pressures
in flowing wells by the analytic zw!t.hod. Neft.khoz. ',I nr-,lf):
45-50 0 163. (WRA 1": 4)

NaMETO I.M. -
Use of the MV-3 van~tor f-3..- usperatwe wasurement in
floving volls* Neftepres, #o1.4 na,407-29 163. (MIRA 171(t)
la Nefteprowilovoys upravlanip %3gobmkn*ftl8*

, - Nowsm, I.I.
Knife wound of the heart and lww. Sas.zed.ibmw. 47 no.l.-92
J&-F '60. (MIA 13:6)
V,
1. In khlrurglchonkogo utdol6ulys 3kd=kDy bol9altay Tatarsh-vy
AM (sav. - 1.19. Astvias.).
(HUNW-WOOM AND M.MMS) (UNGS.-MM AID MTURM.)

85391
O'La
ID
S/079/60/030/006/019/0"VXX
BOO1/BO55
AUTHORSi Kretov, A, Ye. and Matveyev, I, S,
I ----------
V (lWith Ethylene Oxi e
TITLE: Reaction of Cyanamide d
PERIODICAL: Zhurnal obshchey khimii, 196o, Vol. 30, So 6, pp. 1837-1841
TEXT~ Basing on three American patents (1-3) and Refs, 4-8, the &uthors
investigataQ the reaction of cyanamile with excess ethylene oxide in an
autoclave with mechanical stirring a,, comparatively low temperatures
(80-8r,,OC), with and without a solvent. Mixtures of 2--imino-oxazol'.dine
lerivatives were formed in all casea.. The separation of the substances in
the mixture by fractional distillation was not possible since its composi-
tion changed on heating.. At 20001C In a vacuum, only 35-40% of the initial
product 4.s distilled off, the remainder Lives off ammonia and turns into
a solid resinous mass. The mixture was separated chromatographically on
potato starch as anadsorbent and with chloroform, acetone, and methanol
as solvents. The following compounds were se arated and idertifiedt
2-imino-3--p-hydroxy-ethyl-.oxazolidine-1,3 M, . Y-P.-hydroxy-ethyl-imino-
3-pl-hydrory-et',Lyl-oxazolidine-l,"/ (II), 2-N-p-hydroxy-ethyl-imino-3-
Card '112

85391
V. Reaction of Cyanamide With Ethylene Oxide S/079/60/030/006/019il'033/XX
B001/3055
Ik'.51~hvdxoxy-31-oxa-pentyl)-oxazolidirie-1,3 (III). The composition and
oonstants are given in a table. All compounds are easily soluble in water
and alcohcl, moderately soluble in benzene, and insoluble in ether. Above
10000 they gradually decompose. Their structure was verified by hydrolysis
ol. their ethers with an alkali hydroxide solution. The cyclic structure
of the first-mentioned compound is demonstratad by the existence of a
methoxy group in its methylation product (IV). The hydrolysis of the ether
givea K CO methyl amine, and P -methoxy-61-hydroxy-diethyl amine (V),
2 3' P
thus ind-icating an imine structure, Hydrolysis of the dimethyl ether of
the second compound (II) lead3 to compounds (V), (VII), and K 2Co 3' thus
also indloating an Imine structure. H,.tlrolysis of the dimethyl ether of
the third compound (VIII) yields (VII) and (IX)(imino form). Therot are I
table and 8 references: 1 Soviet, 4 German, and 3 US~
ASSOCIATIONi Dnepropetrovskly khimJ.ko-tekhnologicheakly institut
(Dnepropetrovsk Institute of Chemical Technolo
SUBMITTED% June 7, 1959
Card 2/2

S,,'079/60/030/009/020/022/XX
B001/B066
AUTHORS: Kretov, A. Ye.. and MatveZev, I, S.
TITLE: Synthesis of Amino Alooho~.-S~From D,rivativ,is of Oxazolinel
and Oxazolidine. VII
PERIODICAL: Zhurnal obshchey khimii, *1960, Vol. 30, No 9,
PP. 3024 - IA028
TEXT: Amino alcohols of the aliphatic and aliphatic-aromatic series,
which are of considerable practical importance, can be synthesized
from hardly accessible raw materials, or result as end products in low
yield. Particularly complicated is the synthesis of aliphatic-aromatic
amino alcohols (Ref. "he authors devised various methods for the
Gynthesis of amino alcohols of both series, which are based on saponi-
fication of oxazoline and oxazolidine derivatives. The oorresponding
substituted oxazolines and oxazolidines are saponified with a 1.?%
methanol solution of potassium hydroxide and heated on a boiling water
~)ath for 451 - 60 min. Methanol is distilled from the reaction MLxlure,
Card 1/2

Synthesis Of Amino Alcohols From Derivati- 510-!',Ii'60103010091020,10221XX
ves of Oxazoline and Oxazolidine.. VII. 8001/B066
and along with it also the ammonia which is titrated with 0,! N hydro-
chloric. acid. The resultant potassium carbonate is separate.-I by
filtration, dissolved in water, and converted to barium cartonate by
means of ')arium hydroxide. In pure condJtion the amino alcohols are
obtained by fractional vacuum distillation, The primary and avocndary
amino alcohols synthesized are given in Tebla !- The oxazoline
derivatives obtained from styrene oxide and cyanamide are sapoadfied
with 50% aqueous potassium hydroxyl solution by heating for 5-6 hours
on a sand bath. The mixture of the amines forms a viscous matt?r
floating -)n the liquid, The aqueous solution is decanted, and the
carbonate is precipitated with barium hydroxide as barium carbOlLate
The resultant amines are separited by chromatography (with silica gel.)
Benzene, Qhloroform, and acetone served ae solvents, Silica gel and the
mixture to be seDarated are taken in a ratio of 1 : 15. The niti-ogen
content of the primary amino alcohols is determined by Kjeldahl's
method. There are 2 tables and 3 references.
ASSOCIATION: Dneprcpetrovskiy khimiko-tekhnologicheskiy institut
(Dgegropetrovak Institute of Chemical Technology)
SUBMITTED: September 11, 1959
Card 212

MATVEYEV S. 9 CAND %CHEM SCIt OF FHE
REACTIONS OF CYANAMIDE AND CALCIUM CYANAMIDE WITH ORGANIC
OXIDES OR THEIR C.4LORO"YDRINS6$& KHARIKOV9 1961* (MIN OF
HIONEP AND SEC SPEC ED UxSSR* KHARIKOVORDER OF LABOR RED
BANNER STATE UNIV IMENI A. M, GoR'xsy). (KL-DV9 11-6-it2li).
-44-

~ij, A.Teo; MATVE=,Vp i0se
Rea-Ition of cyamdde with prop7lene oxide In an aquems nedilm.
IzTovyv*ucheb.zav,;khimA khIm.tekhe 4 no.3:423-425 161.
(MIRA 14:3,0)
1. DhopropetroveUY Trhimlkc-tekhwlogicheskiy institut imeni
DsandftskoSo, kaf&-Ia-a orgmiicheskoy khimii.
(cyanamide)
(Propylene oxide)

S/081/62/000/021/026/069
all?/2101
AUTHORS$ -JM&tvey4v, J. S., Kretovo A. Yee
TITLE& Synthesis-of nitrogenous compounds from propylene oxide and
cyanamide-an: their reactions.-
PERIODICALs R*f&rativnyy shurnal.. Xhiaiya, no. 21, 1962, IST - 188,
abstract 21Zh1q0 (Nauchn. tr. Dsepropetr6 khin.-tekfinol.
In-t. no, 12, part 2, ig6i, il-- 17)
TEXT& Propylene oxide was proved to react with NZ 2CN according to
Krasuakiy's rule by foraing a mixture of 2-iniio-1,3-oxasolldine deriva-
tives. 0.369 sole of DR 2CN, 0.86k sole of propylene oxi'2, and 50 mg of
Ca(OH )2 are kept in an autoclave for 3 bra at 45 - 750C, the mixture being
atirred every 30 - 40 sin for 3 - 5 sin. Thus a mixture (A) Is obtained
'in a yield of 93 - 97%- Using ;25 ffil C6R6 ( 120 - 1400C 9 3 hrc , 10 - 12 atm)
the yield is 90 - 92%* 11 g of A is dissolved In &Lozano or ocatone,
NK(CX)2 to separateaq the aolvqat Is distilled offg sad 25 al of COGI 5 is
Card 1/4

3/081J62/000/021/026/069
Synthesis of nitrogenous compounds... B1171DIO1
added to the residue. The solution, which is separable after 48 bru, ~s
boiled down to cne-fourth its volume and is examined by chromatography on
ailica gel (column, 65 times I on; ratio of silica Sol to A a 7sl). The
following compounds are washed out as viscous liquidas 1.1 # of 2-IN-1---
hydroxypropyl-5-(21,41-disethyl-3-oza-61-hydroxypentyl)-5-methyl-1,3-ols-
N 20 20
zolidine, C 13R26N20 4 (I~t a,) 1.4840, d 20 1.0"6, using 100 al of petrole-
us ether; 4.4 g of 2-5-F-hydroxypropylinino-5-~-bytroxyprorvi-5-methyl-
20 20
1,3-oxazoliding, C IOR20 120 (lilt % 1.4750, d20 1.1340, using 100 ml of
CHC13; 1.6 g of 2-imino-3- -hydrozypropyl-5-aetbyl-1,3-oxazolid'Lne,
C7H14N20 2 (III)l 20 1-48"t d 20 1.0200, using 65 01 of dioxanei and
nD 20
2-amino-2-cyanmaido-3-~-hydrosypropyl-5-aetbYl-lt3-oxasolidine, C 6H16N 40 2
(IV), using CH 3OH. The portion of A insoluble in CEC1 3 Is extracted with
dioxane, and 1.7 g of III and 2.2 g of IV are separated in the column.
0.048 mole of SOCl 2 is added to 0.03 mole of III, (Semperatare