SCIENTIFIC ABSTRACT USTALOV, V. - USTIASHVILI, A.D.

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• Collection: Scientific Abstracts
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• Release Decision: RIF
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• Document Creation Date: November 2, 2016
• Document Release Date: April 3, 2001
• Sequence Number: 2
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

USTALOVY V.p kapitan
To thp sons about 4,~_a fc-q's of thc-,.ir fathers. Komm. Vooruzh. Sil
46 no,8:64 Ap 165, (YJRA 18t6)

137-58-4-6761#
Translation from: Referativnyy zhurnal, ?Aetallargiya, 1958, Nr 4, p 66 IUSSR)
AUTHORS: Mironov, M.G., Yeliseyev, I.S., Mel'nikov, A.G.,
hroneberg, D.A., Sereda, B,K., Ustalov..-Y-A.
TITLE: Forty Years of Copper Industry in the Ural Region (Sorok let
mednoy promyshlennosti Urala)
PERIODICAL: Byul. tsvetn. metallurgii, 1957, Nr 19-20, pp 55-60
ABSTRACT: Bibliographic entry
1. Copper industry--USSR
Card 1/1

SOV/136--59-4-1/24
AUTHOR: Ustalov, V.A., (Deceased)
TITLE: Contribution# of the Branch Institutes of Ural to the
Developmern-t of Non-Ferrous Metallurgy (Vklad otraslevykh
institutov Urala v razvltlye tsvetnoy metallurgii)
PERIODICAL:Tsvetnyye metally, 1959, Nr 4, pp 1-4 (USSR)
ABSTRACT: This is a review of the 1958 activities of the Unipromed'
and Uralmekhanobr design and scientific research
institutes of the Sverdlovskiy.AMArkhOz -(Sverdlovsk
Economic Council). Theme activities were concerned with
non-ferrous metallurgy in some economic regions of
Kazakhstan and Siberia as well as Ural. The Uralmekhanobr
Institute, in collaboration with works personnel, effected
improvements in ore benefIciation practice at the
Krasnourallskaya (Krasnourallsk), Kirov*radakaya (Kirovgrad)
Pyahminskaya (Pyshft)o Srednev- Ural I sk
Karabashakaya (Karabash), ZolotujNin4kaya (Zolotukha)
and Tuimskaya Beneficiation Works. New equipment such as
the tYpe UM-500 high productivIty flotation pachine wejs--
developed. The UnIpromed' Instituto has cotriiA oxtt
research and design work for the Pya;51,s,,'.j Sredne4Uraltski
Card 1/2 Kirovgr*d and Mednogorsk copper-smelting works. In

SOV/136-59-4-1/24
ContrIbutions of the Branch Institutes of Ural to the D*velopmont
of Non-Ferrolas Metallurgy
collaboration with the Irkutakiy mashinostroitellnyy
zavod (Irkutsk Machine Construction Works) a new type of
grab is being designed. Both the institutes have done
considerable work in the field of automation and
instrumentation.
Card 2/2

1 CIL N-f 4.1LA-1-Al- w-c'm ""T
*0 SPICTRO-MALYTICAL ORT&KNINATION OP THE BASICITY OF OM-
00 IMARTR SLAGI- I- At SHISTSMAN MA 2- A. Q!kt#jq".
0 (tavad:kays Laboraterlys, 1946, TOLIT. 4re, pp. am-601).
0: (In IN 46M)s A method of determining this baoisity of
**A V open-hearth slap is gives in whish the spoebwas in the form
sle
of a sposial briquette, Is exposeld to the "ties of owdevood
sparks, the eallsium and sillsom lines boing aiumpared, The
90-3 results obtained are campared with those of ahomical analysis*
9 ~63
les
Oe
-1* 4 Pw -0
41 0 0 0 0 a 0 a 0 0 0 0 0 0 0 0 0 4 0
0 0 0 egos a a a 0 0 0 0 Ol 0 0 e 0 0 0 0 0 * 0 0 a 0 0 o1
Wes
390
wee
use
Igo

USTAKMY-ZVA2 A. I.
Dissertation: Grad Stud -- "The Process of
Single-Belt Drawing Apparatus." Cand Tech
Vechemyaya Moskva~ Moscow. 8 Jun 54-
Stretching in the Rear End of a
Sci, Moscow Textile Inst, 17 Jun 54.
SO: Sum 318t 23 Dec. 1954

WER/Chemietry - Saccharides
Card 1/1 Pub- 147 - 5/27
Authors Ustanov, Kh* U.) and Kargin, V.A.
Title Sorption of water on melted glucose and caramel mass
Periodical Zhur. fiz. khim. 28/2, 224-228, Feb 1954
Abstract t The sorption and desorption of water by amorphous glucose and carawl
mass was investigated at 25 and 500 C and compared with the sorption and
desorption of cellulose, In contrast to cellulose the glassy sugars at
low relative vapor pressures do not adsorb any water. Sorption begins
at a specific much higher vapor-pressure after which it increases con-
tinuously and reaches values exceeding that of cellulose. The greater
water sorption by cellulose is due to the sturdy chains of its macromole-
cules which prevent diffusion of the water. The mechanism of water sorp-
tion by glassy sugars is explained. Three USSR references (1937-1952).
Tables; graphs.
Institution : Academy of Sciences Uzbek-SSR, Chemical Institute, Tashkent
.Submitted : April 1, 1953

USTANOVIMAYA.I L. T.
Forests and Forr3try - Ukraine
Forests of 3taro-f3erdiansk., Priroda, 41, No. 1,
Monthly List of Russian Acceqgions, Library of Congress, May 1952. UNCLA.'>I;IFIED.

USTAR, Ila da
Microbiological and patho-anatomical considerallions on pulmonary
resection in tuberculosis. Tuborkuloza no.1:13-19 162.
..I. BoInic4 za tuberkulazu i plucne bolevti Tipoloica (upravnik-. Prim.
~-dr. I. Cestnik).
(PIEWITECTOMY) (TUBERCULOSIS PUIEOIWY)

I BENEDIM , ff. j USTAR, He
Sargloal therapy of chronic empywa in pulmonary tuberculosils,
Tuberkuloza 16 no.3t263-265 MY-Ag 164
1. Bolnica za tuberkulozu Topolsica; Institut za tuberkulozu Golnik;
Hirurska klinika Ljubljana.

--.iults of res,~-c' lon ir, the treatment clf pulmcnar~ b~.-rculosis.
(Arlalysil'; of '100 pattents, troated by PUIMOrdAT7/ resf,~ctdor during
the perJcd oV 1956-19610). Tuberkulriza R" '(~4-
holnica za plucnu tuberl-ulozu Toprolsica (Predstulnik: prim.
dr.

SMMIC, Bozidar, Prim., dr.; USTAVDIC, Huhamed, dr.; NOVAKOVIC, Momcilo, dr.
1411, ~!01'1111
Age factor in Indications ! tons, lectomy. Med. arb.,
Sarajevo 9 no.5:77-94 Sept-Oct 55.
1. (Rad Odelanja za. bolesti. uva. nosa, I grla Gradske boln1ce u
Beogradu. Sef: Prim. dr. Dozidar Sekulic).
(TONSILS, surg.
it child., Indic. In relation to age factor. (Ser))
(AGING, pa.thol.
age factor in tonsillectomy, in child. (Ser))

~'C(Cli3.)CH-CHC(C2H5).r,-ri+4H20-
I, diluted by water st'eam ifn the molar ratin 1, 12- 1 ~ 20 Is dehydr)genat-
ed in the presence of Industrial dehydrogenation cataiyst4(K-10 and
Card 1/3 K-12) consisting of Zn, Cr, Fe ancl-JU -oxides activated by K20 f,~r 2

821J47
S 0,1/8 -A' - 2c 40 3
The Methods of Technical Synthesis and the Applicati-In of 2-MethYl-5-EthylpyrIdIne
and 2-Methyl-5-Vinylpyridine
hours at 5754000C and a volumetric rate of 500-600 ml per 1 1 of cata.lyst in I
hour, 97-99% pure 2-methyl-5-vinylpyridine (11) is obtained, yfeld 20-25% based
on I having passed through, or 70-75% based on I decomposed, b. P. 75CC/15
n2OD 1.5454, d420 0.9579. The content of II in the catalyzate 1., 2,3-27%, the
yield of the catalyzate 89-91%. Pyridine, picolines, 2,5-climethyl-, 3-ethyl- and
3-virlylpyridine are formed as impurities. I! is very irclined to polymerization.
0(,-nitroso- IS -naphthol and methol (sulfate ealt of trethylami-
S, C6H2(OH)(NO2)3,
nophenol) are used as stabilizers of II. In the process of 1I separatinn S is
used as stabilizer and methol for storing (in conoentratione of up tc 0.001 weight
%). In the case of oxidizing I by KMnO4 or Cu(NO3)2, 2,5-pyridfne-carboxylic~
acid (yield 60-70%, m. p.2360C) is obtained which is converted to nicotinic acid
by decarboxylizing with a yield ofe-_,100% (m. p. 1630c). The dimethyl ester of
2,5-pyridine.-dicarboxylic acid (m. p. 16300 after reesterification by ethylenegly-
cal is condensed in the presence of ZnC12 into a high-polymeric resin. I with
CH20 forms 5-ethyl-2-vinyl- and 5-ethyl-2-(/~-oxyethyl)-pyridine wlt~, a high
yield. I is easily hydrogenated with a yield of ralOO% by Na 'in butyl aicohcl,
Card 213

8210
SOV;'Bl-59-,~,.20403
The Methods of~Technical Synthesis and the Application cf 2-Mr-thyl-5-Ethylpyridine
and 2-Methyl-5-Vinylpyridine
and also catalytically (in the-presence of Nl-oa?,alysti) lvi 2-metny1-.5--?thy'1-
piperidine, b. p. 160-1610C, n2)D 1.11530, 420 0.8559. 11 is a m-,a--7er for
the industry of synthetic rubber, it car, be -used In the pr~~4uc-',Ir,n of
ard synthetic fibers.
Ya. DanyjstevAly
Card 3/.3

50, 3) SOV/153-58-5-16/28
AUTHORS: Farberov, M. 1. , Ustavshchiko F., Kut'in, A. M.,
P., Yarosh, 'Yer-. V.
TITLE: Techn-'cal Synthesis of 2-Alethyl-5-El.hyl Pyridine and
2-Methyl-5-Vinyl-Pyvidine, and Their Fields of Application
(Tekhnicheskj.ye sintezy 2-met-ILI-5-etilpiridina I 2-metil-5-
vinilpiridf.na I oblasti ikh primeneniya)
PERIODICAL: Izvestiya vysshikh uchebnykh zavedeniy. Khimiya I khimicheskay~t
Lekhnsicgiya, 1,058, Nr 5, pp 92-99 (USSR)
ABSTRACT: The a.7;".hors tcok the synthesis of 2-methyl-5-ethyl pyridine
(MEP) from acetalds'nyde and ammonia with a further dehydro-
genation to 2--methyl-5-vinyl pyridine (M) as a basis for
'he working out of technical synthesis of these tWb substances.
The pape-rs recently published in patents (Refs 11-13) tend to
show an intense elaooration of these reactions. There are,
however, no publications on the first, and especially on the
second stage of thi3 prrcess. The authors first clarified the
most Important rilea governing the reaction between acetaldehyde
and arqmonia for the purpose of an industrial utilization.
1) S Y n t h a s i 3 o f 2 - m e t h y 1 - 5 - e t h y 1
Card 1/4 p y z~ i d 4~ n e. Acetaldehyde is used as paraldehyde. This

Technical Synthesis of 2-1!eth,,1.-5-Zth-._L Fy-ridine and -1-YE-`%-1-::-`-_--:*- .7-;ri~'JLnt~
and Thpir Fields of Application
offers much higher yields. Stoichiometric ratios (1-33 mol
paraldehyde per 1 mol ammonia) could, however, not secure a
sufficiently high MEP yield. The optimum ratio amounts to at
least 4 mol ammonia per 1 mol paraldehyde. The presence of larigE-
quantities of water has a favorable effect. The opinions on tlac'.
formation mechanism of MEP in literature contradict each other
(Ref 14). Up to 30 different salts, among them ZnCl 2, Fe C12'
SbCi 3' COC12 , Ni C121 CH,COONa, NH 4C" CH3 COONH4, NH4Fq NH4F'Hl"
KF, KHF2 and others served as catalysts. A catalyst was selectet_
which corresponds to the techpi.cal process, Its concentmtion.usmllir
amcurtE;tO1-2% of the paraldehyde. The reaction takes also place
without catalyst, however, with much smaller yields.
2) D e h y d r o g e n a t i o n o f 2- m e t h y 1 5
e y 1 p y r i d i n e. S y n t h e' s i s o f 2 - m e t h y 1.
-5 v i n y 1 p y r i d i n e. The best industrial dehydrogena-
A.ng catalysts served for dehydrogenation: K-10 and K-12, which
consist of zinc oxide, chromium oxides, iron and aluminum
Card 2/4 oxide32 activated with potaas_~um oxide. The partial preszure !,a

SOV/1 53-56-5-16/26
Technical SyntL, esi s of 2-Me- thy 11-5-E-,hyl Pyri d ire and 12-Melty 1-5-Vin.y 1 Pyr-f d'
and Their Fie-ids of Applicaticn
best decreased by dilution with steam. Figure 2 shows typical
dehydrogenation curves of MEP (catalyst K-12 at 5750)- Under
optimum conditlicns the IJIVP yields per passed MEP amounted to
20-25%, and per deccamponed AIEP to 7C-75~a- 3) 1 s o 1 a t i o r1
and s t a b i 1 i z a 11 i o n of MVP, i.e. the separation of
MEP f rom MVP is a diffi,'-alt process as theiz boiling points
are closF! to each other (176-7 and 187(j). Furthermore MVP is
easily pclymerized. Pcr this reason a high vacuum is required.
S,ulfur, pi-~ric accid, a--nitrosc-p-naph-thel and sulfurous methyl
amino phenol (Pigs 3,4) were the best stabilizers of some dozens
-'Pvestlgatel. 4) E q i p -,n e n t -and a p p a r a t u a f o r
t h e MVP 3 y ii -'.; 'r e 1 9. Figure 5 shows a corresponding
scheme. 5) The scheme jp 98) shows s o m e m o r e s y n -
t h e ! e a p - o e e e n g f r o m MEP (Refs 19,16).
6) Finally, r u b b e r a n d 1 a t e x t y p e a o n M
basis are discussed. Some of them show better adhesion to cord
from viscose and nyl.:in, high elasticity, frost resistance, and
resistance to Aear and -.ear. Some branches of industry announce
at present a high demand for those rubber +ypes.
Card 3/4 There are 5 figures and 18 references, 6 of which are Soviet.

3OV/153-56-1--!61/12;-
Technical Synthesis of 2-Vethy1-5-Eth:,1 Pyridine ana P-- '. i-el r
and Their Fields of Application
ASSOCIATION: Yaroslav3kiy tekhnologicheskiy institutiopytnyy zavod Ministerst-
va khimicheskoy promyshlennosti (Yaroslavl' Technological
Institute and Test Plant of the Ministry of Chemical Industry)
SUBMITTED: December 28, 1957
Card 4/4

PHASE I BOOK KXPWrTATION SOV/A350
SoveahChAfflilyt po khInA1, tekhnoloE41 I primen*nlyis proizvodnykh
pjrjdIna I khinolins. Riga, 195",
XhImlys, takhnologlya I primenonlye proIzvo4ny;Lh pIrldina I
kh1ftolifta; "terlaly AOv*9Mha.niy* (Chmlstry, Technology
and Utilization of PyrLdino and Q"nollne Derlvatl~es;
Xaterl&ls Of the Conference) Rigs. 124-To AN LA'Yiyskoy
&U, 1960. 299 P. Errata slip Inserted. 1.000 copies
printed.
Sponsortz-4 Menclast Akadtmlya naux lAtviyokay SSR. Institut
V9*1OY=nQYe khlmleheakoye, Cb4hChd0tvO.
Z4..- 3. Bazh&nova; Tech. Ed.j A. IMY&vlnya. Editorial
Board: Tu. A. Bmnkovakly, Cand'date of Chemlstry. X. V.
Van&&&, C"Idato of Cher.Ustry (Pesp. Ed.). I. P. Zalakayev.
Doctor of Chendstryo wkI M. M. Wnjrn'.
PURPOSEt Thin book to Intended ror organic chemists and
engineers.
COVIRAGEr Ttw Collection contains 33 ae-icleo on methods
of synthwel2lng or producing p 1.1ine;.quin ILneonand
their derivatives from matarsly;ource soopors jaities
ft" mentioned. MQMS, tables. and references acc=*&hy
the articles.
11. sn'TEMIC ?TJJ43 OF EnrAlIZO FMVZVA3 L%D
qvlNOLXN&3
_'T_
314pt.ov, A. S.. Lad 0. S. ctrcsto-.-_~(O.
et Lrr~l -1. n1na (~?ntral
'I. V.
A3'.& State Un_-~Orslty syntn'Itir. at'l.1les
C.1-3
A Kut'lh.
And 0'.
cf ttc W.1mi-Itry -f tt-
s-~-th.ft.a of 2-Aothyl-5--,',jlPYrlC I'd
ar.l 2-%cth7-_5_v%r.-,lpyrld_'r0 &rd Their !f Applu,ation 9T
slot-4. Uod"il nxUk
Latviy5koy 33R (In~titutm for Org~nl~ Syn-,h~sjs Qf the
A~&de=y of SIti.1-.3 LAtViy3kaya 33R):. The Tran3itIOM
pM= j,j_ jnj&njcne to PyrLdIne Derlla~l"s
K,t, M, M, jjj~tjtut v7sclc~olek.lya_~Ykh slye-11nenly
ra.1k SSSR (rnstltute CLr R4-&n Molo~~&r Comp~Owdd
Ak.d~-L,
or rt-.e A_Aj_y of USSR)) Syn-h~qjq &~J Polym-ri-
Ztjon Of U,-..%attrrztd Cooomls Oe tt~ PyrIdLne and Q~ImO- 119
A'j'f'hr_T__R_ go1~1&rst"."71 univers-Ltet
127
-3kOkho-7*y3'vthnY7 tnstltut
B
e1
rjt~tu..)j, :asjyt-,~ 3/whes.0 of
Fr=
P-mine3 avl A:-tYl-n4 131
,
-ate Umlvtr~'tYi p"paration or
S I' Alalld~x %ftA 37n-'-hc4%8 Of
m &141= Aly 139
3.11t3
jVj.AcYuzr.'-y
Lm.tltute ror ch-mt:al St'147 Of the
Hydroxyquin,11ine Method of Sinthd3i-i.6, quinallnic Emsee 1~5
Tertol. JR30tov stit, lwv~"Ityl Synth"IM ~r
quinal-n- &nj 3.md *4-Aryllepidind Wto 151
Eatlov I o?.Qmtnv,4h TF4r-ukly gosudamtv nrjy
iciF. in IMAt7pe-m- 'il.'
Catalytic 3;~ th.'es or 2-Phenyl- 5,6-'b.-nzO1QuInOl1"e Derl-
vattives 159
Ardash" V r. (mosto" State Unive"llyl . C&Wytl,2 Con-
-A.;ht0d Ary, Atne* to Q41011.11 171
zaluxa,Tev L. P r I acts or the
.1'atral
17r It

S/080/61/034/003/oil/017
A057/A129
AUTHORS: Farberov, M. I.; Kutlin, A. M., Ustavshchikov, B. F., Vernova,
T. P., Frolov, A. F.
TITLE: Investigation of the conditions for the synthesis of 2-methyl-
-5-vinylpyridine
PERIODICAL: Zhurnal prikladnoy khimii, v. 34, no. 3, 1961, 632 - 640
TEM Dehydrogenation of 21methyl-5-ethylpyridine (MEP) was inve3tigeted
in ordor to increase the yield of 2-methyl-5-vinylpyridine (MVP). Conditions were
presented ensuring a 25 % yield of KVP in relation to the amount passed of VLEP
and 70 - 73 % yield in relation tb discomposed MEP. Steam effects partial hyd-ro-
lysis of pyridine bases and ie thus not a completely inert diluent In dehyrh-ogen-
ation of MEP. Inhibitors far polymerization were investigated for the sterage
of MVP and separation from dehyd:-ogenation products. Improvement of thii3 ldehyd-ro- /
genation process is important for the manufacture of polymer materials. MVP is
especially significant in the produc-Aon of special types of synthesized Istex
and synthetic rubber according t-3 R. Frank et al. (Ref. 1: Ind. Eng. Chsm., 40,
879 (1~948)), J. E. Pritcha-rd and M. H. Ophelm (Ref. 2: Ind. Eng. Chem., 46. 2242,
Card 1/9

S/080/6l/034/co3/o*_n/oj'7
Investigation of the conditions for ..... A057/A129
1954, 47, 863, 1959, H. E. Rallsback and C. C. Biard (flef. 3: Ind. &jg. Chem.,
48, 1o43, 1956),and V. L. Tsaylingol'd et al. (Ref. 4: Kauchuk i rezina, 9, 1958,
3, 1959, 9, 1959), or ion exch&nge resins in the manufacture of synthetic fibers.
The raw material - MEP - is synthesized by Chichibabin's reaction between paraal-
dehyde and ammonia in liquid phase according to M. 1. Faberov et al. (Rfif. '5:
Izv. Vuzov, Xhim. i khim. tekhn., 5, 92, 1958) with a 70 - 73 % yield. 7n;~ pre-
sent experiments were oarried out (in asaistance of M. Yu. Tikhvinskaya and M. A.
Loginova) by a method and with a laboratory assembly described in a prior paper
(Ref. 11: ZhOKh, 30, 875, 1960). Vapor pressure and liquid - vapor equilibria in
the system MEF - MVP was detsrmlned on an apparatus similar to Oth-nqr's (R~?f. 12:
Ind. Eng. Chem., 45, 614, 1953) especially adapted for vacuum tests. Two ~~ata-
lysts were usedi no. 1 based on ZnO and no. 2 on Fe203, containing 86 - 88 % of
the basic component, some cbxomium oxide and small amounts of other componsnts,
which are not specified. Since considerable carbon deposition occurs during the
dehydrogenation process, the catalyst had to be regenerated after 2 - 8 hours
by passing an air-steam mixture at. a maximum temperature of 6500 - 7000C. Re-
sults of dehydrogenation experiments with steam as diluent in varying conditiorLs
are given in Table 1, It can be seen that the yield of MVP related to d9compo-
sition of MEP decreass with the conta_ot time. This is apparently effected by
Card 2A

S/080/6-1/034/003/01 t/-Q 17
Investigation of the conditions for A057/A129
side reactions and inareasing carbon depoeltion. The.latter depqndq on the type
of catalyst andthe degree of dilution by steam. Steam cannot be considered as
inert diluent, since with increasing :dilution by steam the yield of catalyzate
and of MVP (based an decomposed MEP) decreases, in spite of the fact Lhb*l thi
yield of MVP based on the amount of passed MEP increases (Figure 1). Also with
increasing dilution by steam firmation. of gaseous products (CO2, H2, N1'3 '-+a)
and the content of pyridines ( 0.- and 4Y -picoline,,2,5-lutidine, 3.-vinylpyri"
dine) in the catalyzate increaze-_ This can be explained by the reacticri of py-
ridine bases with steam, r-walting -in a, partial dealkylation of MEP and fc rTa7don
of pyridires, or total rupture of the pyridine ring with ammonia evolution. A
similar reaction was observed by A. A. Baladin et al. (Ref. 8: DAN SSSR, 1!", 79,
1956) on cL-picoline. These sids re&ctdons of hy4rolysis occur with. di-Cfe-int
rates on various cattalysts, thus influencing the selection of the lattr7r. Re-
sults on dehydrogenation of MVP with othQr diluents are given in Table 3. The
observed effect of benzene can be axplained by the fact that no side reactions
of hydrolysis occur. Althcugh nitrogen does not show these side react.ions, no
desorption of pyridine bases from the catalyst is effected by nitrogen (contrary
to benzene) resulting in thermal decomposition of these substances. Practiona-
tion of the catalyzate at 20 torr demonstrated that the fraction boiling at 63
Card 3/9

S/080/6!/O-i4/003/o"Lj-/017
Investigation of the conditions for A057/A129
-90C.(20 torr) [Abs. a I-er's no-e: E-ror,..In original paper - 2~QQ torr instead
- 6 tr c,4
of 20.] has an increased refraction Indey,.and contains conpiderable amounts ofen
unsaturated compound, apparantlY 3-vinYlpyridine. Thus the following reaction
and side products were obtain-~id In del'~ydrogenation of MEP: (I) M-picolin-~-, ( 'I!)
3-ethylpyridine, (III), 2,5-lutidine, CTV) 3-vinylpyridine, (V) 2-met1W1-5-1!t'nyl-
pyr~dine, (VI) 2 "%-metbyl-9-irIriy1pyrid1n(!.. The present authors consider (1), (11)
and..(.IIL) as main crackin i-'e (:LV)
,g produnts of MEP (in presence of hydrogen), wb
is a eracking produ.-,t of MVP.. Different stabilizers for MVP were invautigated
(Figuye 3) and it was observed that 0.1 % of sulfur is the optimum stabilizer in
fractionation of MVP. For the storage of MVP an.admixture of 0.001 % methol iZ
most efficient in e,abil~~nw MVP for seviwal weeks, or 0,01 % methol for ;7-~!veral
monthsq, Liquid-vapor equilibrium in the system MEP - MVP is shown ih Figure.5.
Corresponding-expariments demc-nstrated that apecial conditions must be Mafnt&ined
if a 98 - 99 % concentration of MW shculd be attained in fractionation. Thus in
the system the maximum tampsrature should be 950C (for highly concentrated MVP
only 8500, and highly effective inhibitors should be used. There ars 6 fig-,jr9s,
4 tables and 12 referencest 8 SOVJ,~14;-bloc and 4 non-Soviet-blor-
card 4/9

P S/080/61/034/003/01-1/617
nvestigation of the conditions for ..... A057/A129 '
ASSOMTIONS: Institut monomerov dlya SK (Institute of Monomers for Synthetic
Rubber) and Yaroslavskly tekhnologicheskiy institut (Yaroslavl'
Technological Institute)
SUBMITTED: June 6, 196o.
Table 1: Dehydrogenation of 14VP on the catalysts no. 1 and no. 2 using steam as
diluent. Legend: (1) no. of the catalyst, (2) temperature (00, (3) nominal con-
tact time, see., (4) volume velccity of the 14EP supply (in ml/ml catalyst per hL
(5) molar ratio H20/ MEP, (6) yield of the catalyzate (weight %), (7) yield of
MVP based on the MEP passed (mole 5), (8) yield of 14VP based on the 14EP decompos-
ed (mole %), (9) carbon deposit on the catalyst (mole %Jbased on the I-T-T passed).
Card 5/ 9

USTAVSHCHIKOV B.F.; FARBEROV, M.I.; PODGORNOVA, V.A.
-- I- - .9
Industrial synthesis of methacrylic acid based on isobutylene.
Khim. i khim. tekh. lt79-89 162. (MIRA 17:2)
1. Yaroslavskiy tekhnologicheskiy institut i Nauchno-issledo-
vatel'Bkiy institut monomerov dlya sinteticheskogo kauchuka.

USTAVSHCHIKOV, B.F.; TITOVA, T.S.
Transfomation of bivirLyl adducts with furfurol by the
Cannizzaro-Tishchenko reaction. Khim. i khim. tekh. 1:109-
110 162. (MIRA 17:2)

ACCSSSICS IMs A2602"22 S/30V/62/001/000/0079/0069f
i
AUTHOR: Ustavshcbikow. 3. F.; Farberov, M. I.; Podgernows, V. A.
M=s Technical synthesis of methacrylic acid based on Isobutylene
i tz .
~,SOLTRCZ: Yaroslavl'. TakhnologicheskLy institut. Xhinlys i khtafthaskaya,
tekhnologiya, vol. 1 (8). 1%2, 79-199
TOPIC TAGS: methacrylic acidg toobutylcme, synthesis, monomer# nitrogen tetroxide,
,nitrosation, isobutyric acid
ABSTRACT: Methacrylic acid and its derivatives are one of the most important nono-
,mers for the production of synthetic materials. The requirements for methacrylic
derivatives, in the Soviet Union alone, will increase ten fold within the next 20
years. Currently there is one method of obtaining methacrylic acid and methyl
methacrylate based on the use of acetone and hydrogen cyanide as an initial raw
material. The authors conducted a detailed study of the method for obtaining
methaerylic acid from isobutylene and nLtrogen tetroxide. The reaction was shown
.graphically along with the various effects of temperature and velocity on the yield.
Diagram of the equipment used were given. The conditions of the isobutylene reac-
.tion with nitrogen tatroxide produced a-oxybutyric acid with a 754% yield as a
1/2

'ACCESSION NR:----AT4029922
:'basic product. A nitrosation reaction occurred rather than a nitration reaction.
The fundamental intermediate product of the reaction, a-nitrate Isobutyric acid was
f ormed f rom the isonitroso ~ompound-oxitse of a-nitrato isobutyric aldshyde. The
-catalyst and conditions were selected which permitted methacrylic acid to be ob-
tained from a-oxyinobutyric acid with a yield approximating the quantitative. Orig.
art. has: 6 figures.
ASSOCIATION: Yaroslavskiy takhnologichookiy institut I nauchno-iseltdovatel'skiy
'inatitut konomerov. dlya SK (NEW) (Yaroslavl technological institute and scientifin
.research institikta,pf sonowers for SK
t~SUMTTKD: 00 DATE ACQ: 29Apr64 ZMCL: 00
'SUB CODEt CH NO R191F SOV% 006 ODMR: 006
ge!td 2 2

S/204/62/002/004/015/019
Synthesis of methacrylic acid ... E075/E436
NH40H to solutions of CaN03 and CaC12- It is dried at 110 to
1200C and activated and regenerated at 350 to 400*C in an
air-steam mixture. The dehydration is achieved by passing 20 to
301,1 aqueous solution of a-oxyisobutyric acid over the catalyst at
25~ to 3000C. The products contain 10 to 15% methacrylic acid.
The yield increases with increasing temperature up to 2500C, which
is the optimum temperature for the process. The optimum space
velocity for a-oxyisobutyric acid is about 1.3 litres/litre of
catalyst/hour. These conditions give 77-Via' yield of methacrylic
acid (based on the amount of a-oxyisobutyric acid passed).
There are 4 figures.
ASSOCIATIONS: Yaroslavskiy tekhnologicheskiy institut
(Yaroslavl' Technological Institute)
Nauchno-issledovatellskiy institut monomerov dlya SK
(Scientific Research Institute of Monomers for
Synthetic Rubber)
Card 2/2

USTAVSHCHIKOV, B. F.; FARBEROV, M. I.; PODGORNOVA, V. A.
SYnthesis of methacrylic acid based an isobratylene. flefte-
khimia 2 no,4:592-399 JI-Ag 162. (MIM 3-5: 10)
1. Yaroslavakiy takhnologicheakly institut i Nauchno-iasledo-
vatellskiy institut monomerov dl7a sintetichoakogo kauchuka.
(Methacrylic acid) (Propene)

FROLOV, A.F.; LOGINOVAP M.A.;.UNAVSHCHIKOV, 13-f-
Separation of methacrylic acid - vater mixtures. Neftekhiaiia
2 no.5t766-770 S-0 162. (KULA 16:1)
1. Yaroslavskiy tekhnologichaskiy &stitut.
(Nethicrylio acid)

IJSTAVSIiCHIKOV; B.F.; PODFORNOVA, V-A-j DOMIDONTOVA, N.V.; FARBERCT.M.I.
Cola,roe Of the reartion between simplest 0~-Amfins and
liquid nitrogen tetroxide. D)klo AN SSSR 157 no.-ItW-146
i1 164 (WRA 17:8)
1. Yaroslavskl..y tekhnologi-.hesk-.y instituto Prodstavlano aka-
demikom M.I. Kabac,,hnikm*

USTAVSHCHIKOV, B.F., kand. khim. nauk, dots., red.; ISM40,
1i.V.0 kand. fiz.--mat. rauk, dots., red.
[Authors' abstracts and theses of papers presented at
the 14th Scientific Conference of the Yaroslavl Tech-
nological Institute held in 1962] Avtoreferaty i tezisy
dokladov. lAroslavll, Y-vo vysshego i sredne 0 spetsiall-
nogo obrazovaniia RSFSP, 1~b2. 103 p. &IRA 17:3)
1. Yaroslavl'. Tekhnol~.,gicheskiy institut. Nauchnaya kon-
ferentsiya. 14th) Yaroslavl', 1962,

. T: : R , V Ylk
I., L
Pol-arograpKIc study cf trie k.Lnet.',:Z- '-,ydrnly, 314~, of n
acid e3tors, Part 1: flydrolyoiq of isob-Lity-ric
Kin. i Kat. 5 tio.3:552-555 t~j-,Jle 16i..
1, Yaroslavskiy tekhnolcglch(:2kiv instAr--it
tel'skiy inetitut moncrrarov diya S4~LteTjCj,,eSir-)k!,C n.

FROI,OV,l A.F. -, LOGINOVA , m.A . - B.F.
Liquid - liqAd equilibrluai in thp, oyqtem acetic acirl - nil-ric
L
acid - water - chloroform. Zhur. fiz. khlm. 38 no.7:1837-1839
i1 164. 18: 3)
1. Yaroslavskiy tekhnologicheskly inatitut.

USTAVSHCHIKOVV B.F.; FARMOV5, F-I.; TITOVA, T.S.; DEGTYAREV, Ye.V.
Nicotinic said. Metod. poluch.1him. reak. i prepar. no.11.,
82-8.3 64. (MIRA 1811121)
1. Yaroslavskiy tekhnologicheskiy institut. Submitted April 1964.

B.F.; NSKITINA, N.2
Frio!iov A . F. Y -i R1 F fl, V A , M .4 IV,
Li -'-liquid equill bri%,m in -h5 SYstam =ethyl "t-hacrylat-c -
tiietbyl alcohol - wat6r. Iz-.r,v-j-s,.uzheb.zav.i kt~~mi khlm.tein.
8 no.4070-573 065. (KIRA 18sli)
3. Yaroslavskiy- tek-hnologicheakiy i-n6t!tut,, kafedra tekhnol--gil
.4ogo organlchas~cgo sint-aza 3. siriLetichesk-cgo kauchuka~

L 13497-& ENT(R)/HWP(J
-ACC- Nits- A'P60-02074
HM
UR/0204/65/005/006/0873/0979
SOURCE CODE:
AUTHOR: Ustavahchikov, B. F.; Podgurnova, V. A.; Dormidontava, M. V-;'
Faberov, *F--f7l---
ORG: Yaroslav Institute of Technology (Y roslavokiy tekhnologicheskiy
institut) -- 1~4
TITLE: Synthesis of methacrylic acid t'sed on isobutylene Reaction
mechanism of isobutylene with H204
SOURCE: Neftekhimiya,'v. 5, no. 6, 1965, 873-879
TOPIC TAGS: chemical reaction, IR absorption, isobutylene, nitratioT
nitric oxide, IR spectrum, spectropbotometer , acrylic acid, organic nitroso,
compound, nitrate
ABSTRACT: The mechanism of reaction of isobutylene with liquid N204 wa!
studied by examining the IR spectra of the reaction products. The ob-,
ject of this work was to examine the feasibility of synthesizing met-ha-
crylic acid by reacting isobutylene with liquid H204- The IR absorptioi
spectra were taken with IKS-14 spectrophotometer with a NaCl prism. Thi
polarographic analyses of the reaction products were made with a VHR po-
larograph made by Orion Company. The reaction was conducted at OOC and
at 200C in dichloroethane solvent. The nitrosonitrate of isobutylene
1/3 UDC: 547.391.3.05:547.313.4-125:546.174

L 13497-66
ACC M AP6002074
was detected in the product only whan the reaction was conducted at OQC.
It is claimed that this nitrosonitrate represents the primary reaction
product. Reaction of isobutylene with liquid N204 is shown in fig. 1.
The authors thank Ya. 1. Tur'xan fo-,:, valuable consultation and polaro-
graphic analysis of the reaction products. Orig. art. has: 5 figures,
I table.
2/3

L 13497-66
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Reaction of isobutylene with liquid N2Qjs
SUB CODE: SU13M DATE I .13liar6.5 / ORIGREFt 008 / OTHREF: 006

FROLOV, A.F.; LOGINOVA, MAi.; IJSTAVSHCIIIXOV, B.F.
Oeparation of mixtures of asatit and nitric acido, Zhur.prikl.khim.
38 nio.6:1386-.1389 ~'e 165. (~ff RA 19 110)
1. Taroolavskiy tekhnologlcbsskiy institut.

FARUROV, M.I.; USTAVSHCHIKOV, B.F.; TITOVA, T.S.
JAgainchomeronic acid. Votod. poluch. khim. reak. i prepar,
no.1108-59 164. (MIP-k M12)
1. Yaroolavskiy tekhnologicheskiy Institut. Submitted April
1964.

FARBEROV, M.I.; USTAVSHCHIKOV, B.F.; HVIRf A.M.j BARANOVA, T.I.
Isocinrahawronic acid. .)Ietod. 7poluch. khim. reak. i prepar.
no.11:60-62- 164.* (MIRA 18:12)
1. Yaroslavskiy tekhnologicheakiy institut i Hauchno-issledovatell-
skiy institut monomerov dlya sinteticheskogo kauchuka.

FARBEROVY M.I.; USTAYS11CUMV, B.F.; KUT-IIN, A.M.; BUKHAREVA, V.A.
5-Ethyl-2-( 0 -hydroleth7l)-pyridine. Ketod-poluch. khim. reak.
i prepar. no.,1:10b-10L9. 164- (MIRA 18:12)
1. Yaroslavskiy tekhnologicheskiy institut i Nauchno-is8ledo-
vmtellskiy institut monomerov dlya sinteticheakogo kauchuka.

RUSAKOVA.. M.S.; TURIYAN, YA.I.; ILSIAV4H HIA
qj_ 0
jf*jj,
Folarography of nitric aefd eaters. Mechanism of electroreduction.
glaktrokhimiia 1 no.7:854,-857 JI 165. (KIRA 18:10)
1. Yaroslavskiy tekhnologicheskiy institut i Yaroslavskiy
nsuohno-isoledovateltakiy institut monmerov.

USTAVSKIlIKOV, B.F.; FOIIGC-!iIT0VA, II.A.; DOP1,11DO"iTOVA, N.V.; FARBEROV, M.I.
. I -
Synthesis of methacrylic acid based cr, -1--olmt--riene.
of the reaction of isobutylene with N2G4' Neftekhimiia 5 n0-6:
873-879 N-D 165. (MTRA 19:2)
1. Yarosl,,vvskiy instltut. &,ibmi"ted M'Irch 13,
3965.

AUTHORS: Kryukov, S. I. , Kut' in, A. M., Levskaya, G. S. , 153 -58-1--13/29
Tepenitsyna, Ye. P.,,Ustavahchikova,-z. F., Farb~_-rov, Y. I
TITLE: An Improved Method of the Synthesis of Triethyl-Aluminum
(Uluchshennyy sposob sinteza tr:;.etilalyuminiya)
PERIODICALs Izvestiya vysshikh uchebnykh zavedeniy,
Khimi,ya i khimiclieskaya tekhnologiya, 1958, Nr 1,
pp. 86-93 (USSR)
ABSTILOTt The authors give a survey on the publications of trialkyl-
aluminum as specific catalyst, both alone, as well as with
cocatalysts for olefinic polymerization (references 1 to 3),
and they compare with each other the known methods of
production of aluminum-organic compounds (references 4 to 6).
The authors selected the method by Grosse and Meviti
(Mavity, ref- 5) as the most convenient one. A)- Production
of ethylaluminum sesquichloride (mixture of ethylaluminum-
-dichloride and diethyl-aluminum-chloride). The first stage
of the process according to reference 5 proved to be rather
incomplete. It is difficult to be controlled, has a long
period of induction and often leads to the complete
Card 1/4 destruction of the products, sometimes with explosion. The

An Improved Method of the Synthesis of Trio thyl-Aluminum 153 -58-1--13/29
authors tried various initiators at atmospheric pressure
(crystalline iodine, ethylaluminum-sesquichloride, ethyl-
bromide and a mixture of these substances). Table 1 shows
the influence of individual initiators on the period of
reaction. Ethylbromide acted most effioiently. Table 2
shows the influence of the initial temperature with the
supply of ethylchloride on the reaction-period. Optimum
conditions for the carrying out of the process were selected
from the obtained test results. Further tests were carried
out on an enlarged plant (figure 1). The laboratory results
were confJrmedt It was possible to reduce the reaction-
-period to from 2 to 3 hours. B)- Reaction of symmetrization
of ethylaluminum-sesquichloride. In order to obtain tri-
ethylaluminum, the above reaction must be carried out
with the participation of metallin sodium. According to
reference 5, various insufficiencies exercised a disturbing
effect in this connection. The authors found the conditions
for removing them: 1)- Sodium ought to be used in fine
dispersion, the surplus of Na must not exceed 5 to 10% of
.the theoretically required quantity. 2) - Sesquichloride
must be introduced in portions as a 20 to 30% solution in
Card 2/4 hydr-ocarbons- 3) - The temperature of reaction must not

I ~
An Improved Method of the Synthesis of Triethyl-Aluminum 453-58 - ~ - 13/ 29
exceed 1300 and an intense agitation should be guaranteed.
The gasolin&traction "galosha" (boiling above 1000) proved
most effective among several tested solvents. The yield of
triethylaluminum. amounted to 70 to 76% of the charged
sesquichloride under the selected optimal conditions. A
certain quantity of partly oxidized triethylaluminum was
proved in the produced triethylaluminum. The inactive part
of the catalyst formed a mixture of all 3 possible ethoxy-
-compounds. An experimental part follows. C) - Production
of aluminum sesquichloride. According to the method described
here, a 99~ yield of that theoretically possible was
obtained. The two (paragraph A) components were present in
the mixture in approximately equimolar quantities. D) -
The reaction of aymmetrizatioti was carried out in a device
shown in figuro 3- A filter required for this purpose is
shown in figura 4-
There are 4 figures, 2 tables, and 12 references, 3 of
which are Soviet.
ASSOCIATIONt Yaroulavokiy tekhnologicheskiy institut i opytnyy zavod
Card 3/4 Ministerstva khimicheakoy promyshlennosti. Kafedra

An Improved Method of the Synthesis of Triethyl-Aluminum 153 --58-1--13/29
tekhrLologii ounovnogo orgadchuskogo sinteza i j],
V11 TeChnoloEjCal Tp
(Yarosla - Z*it,.;te and
the Experimental Plant of the Ministry for Chemical Industry,
Chair for the Technology of General Organic Synthesis
and SK)
SUBMITTED: September 23, 1957
Card 4/4

Sil, 08, .17/ 'rj
A0061AC01
fr-.r., Referativnyy zhurnai, Khimiya, 19,15,0, Nc;. 17, P. 372, # 70452
A UT: 4 OR Likov, 3.1. '. Ku-~'yin, A.M., Levskaya, G.S., Tepenitsyna, Ye.P.,
Us-~avshchikova, Z.F_ Fartercv, M.I.
TITU Te~,hnl.cal Mcde of Tr!9thv1al,,Lninum Syntbesis
PEK-ODICAL! Uch. zap, Piroslavsk.-,-19khn,~l, ir..+-a 1959, Vol. 3, PP. 5-17
TEXI'- -The devei-,ped a technical mcde of preparing ethylaluminum-
--!de (:) W-_- a ylz,~%'_; ::f ab:wut 100% cn the tasis cf a method deEcribed
A.U., Ma:;'-ty, J.M.,, Organ. Crem., 1940, N,:,, 5, p. 196) which consists
fT-r% and A! in the Pri-sence Of 5-10% C H Br (Iln)
in ~re in-erac*,!:r,1:,f C2t5C' X- 2*
wll~, r~_Ian!-_n -:. Al. s iniltors yield.-
In and "heIr mixtures were tested a
ing insati5fas'-.ry res-Ilts. is assumed that the prc.,~ess is initiated by inter-
f:-rm!nv_ In 1!*.he case that III is used. I is
tra%_- f- r:nr 4 -,, f,- F ) Al by rr:~-CA_ ~_sillng w-1 -.h 111--peried Na metal in organic
2~5 3 n-), Na is taken in
(t_nzine.r-1't_-sr. refL-.~d kerosene, xylene, li~-cctaze
'f 5-15%~ : L': 'htl rea:ti-n by p~r'!,1--nE In the fcrm Cf
C.

-a I Y:d~ ~.-f TT I a -hy'-*' a.. _T._!n--.;rr. Syn-,eelzle A0061AC01
2~~ .30% n rylr: - a_-b_-n, the yield :~f Tv is 70-76% in reiati,~n to I, and
70% 1.r. -~ c_- Al. All -.he experiments are ca-r-r1ei out in dry N2
a*~n-S;h-_,re, fre= :~f knl-unts 3f 40 g Al and 24 g =I are heated, while stir-
r.ir.g, 5GOC ani i6o-g (iic.%) 'I: is aidsd by portions of 10 ml~ the reacticn
laz'~ 8 c.':1-aln,~-d In the form of a colorless or slightly colored
llq~!!, tne 99%, bc~Illng temperature 117_1220C/50 mm. ' In 100 g of the
1. 1 is added
29 g Na v~ heate_4 a-!~ 1000C., int. '~he hct dispersion 9 4 g
da-ing 90 min in -he f~~rm --f a 30% s,_`_utIcn in benzine-rubber (boiling temperature
100-11~~C), mixed f:r 30 min~;-es at 105-110c-l and filtratie-42 'he prezipita,:~e is
waz-hed wI-,h 250 X_ 0, s:lven,~; :71 is -,~--btained in the fcrm of a colorless liquid,
self-zilt.I.A.mating -6r.. air, the yield is 32.5 9, the bcIling temperature 100-1070C/
10 mrr., d 0.872. The auhcrs present two tables and schematic diagrams cf metallic
apparatus an4- eqilpmanf, Inz_luding deEcriptions.
S. Davydova
Translat:r's- n--te% ThI5 is the full translatinn ~;f the original Russian abstract.
Card 2/2

JX,VW.-Fl',TC,, P..V.; KUTII.., UI>TAVSHCHIKOVA
FARBEROV, M.I.
S..7,thezAs of tert-butylben.--cie !zv.vys.uchab.zav.;
toldi. 4 nc .3: /;"--4f-7 5 161. ("121 14:10)
1. Yi~roslavjkiv Inatitilt i
Anstitut zicnr),,.ierov dlya ,;intcticha:A:uio lauchuka,
kafr~dra telzhnologii osrovno-r~o organicheskogo sinteza i
sj-Tltetich~,shc;:O
(Renzoic

~J-STAVS HCH IIE OVA, G.V.,
G. G. Ukz.OV, Tzvotnuin bletril. 10, No. 6, 109-30,
(1935)

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FRO:,Iwp LOCINOVA, IM.A.; AIVIIIS,W, O.K.,, U10'AMCPIKOV~ B.F.
l,'.qu.'ci- vapor eTallAbrium in thm 073"OM methy! alcohol -
methyl methacrylate. Zhur. fiz. Mir,, 38 not5gI303-I"04
My 164. (WRA 18:12)
1, Yaronluvskiy tekhnologichoskly Inatitut. LubmAted
June 7, 196).

SHUBENKO, V.A~; USTFUMOV, V.N-.-' - -
Devices for measuring the pressure exerted by the metal on the
rollors !Ln rolling operations. Trudy Ural. politekh. inst.
no.106:137 -l" 160. (MIRA 15-5)
(Rolling milli3---Zlectronic equipment)
(Electronic measurements)

S A jjj':'~V '!7. " . .' . : I - ~ 1-1 ENTSEV A. .1.
I --co&;` in bodies of water of the 1~:-jsr CO tnl
, in the f Ltl
1,~-,;L-r irtush Plverv and samo cl:ay-rctcr'Lttic;s of It's dorelcm-3rt.
I
Gool. zhur. 41. ne.6,*818-R25 '65- (KirPA 18110
1. rc3udar.,ttvennyr nauchno-ins).-dovatolltikly Institot curnogic, i
rAnbnogo r.71mjrr-- '(bczyaystvu, l4ningrad.

UTEKHIN Be P. and BAKEMA E. N.
Res* Inst. for Pig-husbandry# Poltava. * Method of investigation of intestinal digestion
In pigs FIZIOL, ZIRM, 85SR 1954, 40/2 (236-236) Illus. 2 (RuBsian text)
SO: E=ez$a Medica Section n Vol 7 N, 12,

XAPJLD, V. Is.; PALATM, 1. S.; LOMM, D. P.
"An investigation of heat and mosentm transfer Pwossos In A gcW ssible
turbulent jet 1-1 a unifors flow.-
report submitted for 2od ALIJAion Coof an Heat A Meat TransOyr , HW~k, 4-12
May 04.
Fomr Inet, AS IrAzSSR.

.-USTENK -inzhener-kapitan
A strong wind and the mooring of a helicopter. Vest. Vozd.
Fl. no.12t6l-63 D 161. (WRA 15:3)
(Helicopters--Maintenance and repair)

ZAGORDAN, A., inzh.-podpolkovnik; USTENKO, A., inzh.-kapitan
To the pilot about the MI-4 helicopter.
87-88 J1 163.
4Helicopters)
Av.i kosm. 46 no.7:
(NIRA 16:8)

USTENKO, A. A., Card Tech Sci -- (diss) "Research into the ifiechanit3iri
of foramtion of fibers in the production of mineral and glass wool by
draft method." Moscow, 10,60. 1~ pp; (Ministry of Higher and Se-co.-.dar,-~
Specialist Education RSFSR, Moscow Order of Labor Red Banner r1onstruc-
tion Engineerin Inst im V. V. Kuybyshev); 200 copius; price not given;
(KLI 22-60, 1395

USTENKO, A.A., kand.tekhn.nauk
I------ di~udj` of the fiber-forming mechanism in the production of mineral
and glass wool. Stroi.zat. 9 no.902-35 S 163. (MMA 16slO)

HARBARINA) T.M.; BUBYRI, N.F.; LjU'-'T, LJ'..; VEL"OUKIY, V.N.;
GORLOV, Yu.F.; G.'-11IBfiJ4OVS"I'Y, V.G.; DqOZDOV, 1.Ya.;
YEREI-T;P I.A..' ZEZI?;) KEEVESP, P.D.; KOC11MM. E.F.;
KOSYREVA Z.S.; LEM!, S.N.; J.!~KWIMICH, A.T.; 11,"ERZLYAK,
A.11.; HODOV, E.S.; ROZIDIOV, A.I.; SEREBRYANSKAYA, B.I.;
SUKILAM, M.F.; US1ENKQ,,A.A.; KIMMIKO, Z.S.) 311MIDT,
L.M.j ETI11, A.O.; YAKEONTOVA, 11I.Ye.; KITAYISETV, Vladimir
Andreyevich) prof., dakt6r tekhn, nauk, red.; ARPETAYEV,
B.G., glav. red.; TROKEIMOVSKAYA, I.P., zam. glav. red.;
FUIAMMKO, I.V., red.; KITAYGORODSKIY, I.I., red.;
KRZHWINSKIY, S.A., red.; HOUVARM, Ye.L., red.;BALATIYEV,P.K.
red.
Nanual on the manufacture of heat insulating and acous-
tical materials] Spravo2hnik po proizvodstvu teploizo-
liatsionnykh i akusticheskikh materialov. Moskva, Stroi-
izdat, 1964. 524 P. (mim 18:1)

USTENKO, A.S.
Lighten the load of trac7twalkers. Put' i out. khcz. no. 8:43
49 158. (MIRA 11:8)
1. Zamestitell nschollni'cs d1stantaii puti. stantsiya Kurort
Borovoye Kazakhskov dorogi.
(Ra Ilroacls-Track)

ZAY-,SZV, A.; SIKLTLISKIY. I.; SKOBNLKIN, I.; USTOKO, F.: YNGOHOV, V.; ORLOT,
A*; 312MOVS So
Free the state Bank fron nonbanking functions. Dan. i kred. 16 no.l:
51-55 Ja '58. (MIRA 11:3)
(Bankis and banking)

do
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air A!2 )my gepto
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CLASUPKATICS
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FAVIA)V# A*V,*; CUTSIZO# 04P*
Best bmlanm and mdiatim rogim In oorn flolde, bro All
S=.i ser. Mwo no.6$47-55 R-D 10o (HLRA 18:U)

PAVWV, A.T.; USTENKO. G.P.
Some features of the formation of the potato harvest under
Irrigation in the Southeast, Yiziolarast- 7 no-I:IGO-103
16o. (MIR/i 1315)
1. Stalivgrad Agriculti=al,Inctituts.
(Volga-Don Canal region--Potato)

KARPENKO LcP,; PLYASKIN", Y~.i.A.~ USTENKO, G.P,
11
e-oazErcia-' usq c.-f efEvt.- trays witi- teffie elements. fleftei
n6ftekhim. no.7-.LO-43 164.
1. NBkAy neftepor,?c-vbatyvap-ishchiy zavocl.

SHUGAYLO., V.T.; 1~37EXLO)~U. ?~,
Sensitivity of dysentery bacteria to antibiotics; from dateL
of the Ternopol regional hospital from 1959 to 1961*
Antibiotiki. 8 no.lt68-69 Jat63. (MA 16-.6)
1. Ternopoltakiy meditsinakiy institut i Oblastnaya sanitar-
no-epidemiologicheskaya stantsiya.
(SHIGELTA) (MITIBIOTICS)
(BACTERIA-MYECT OF DRUGS ON)

USTUKO, P*K*
Aspects of growing suVw beets. Sakh.prom. 31 ne.3:48-52 Mr 037.
(MLRA 10:4)
I,Svmsko-Ste]p&novskly sakharan savod,
(Smar beets)

LAZAREW, A.I.; IAZAREVA, V.I.; ZAK, S.Sh.; USTENKO,, T.M.
Determination of rhenium. with M-furyldioxime after -the separation
of molybdenum by the extraction with a chloroform solution of
nitrone. Zav.lab. 28 no.11s1316-1319 162. (141RA 15:11)
1. TSelinogradskiy sellskokliozyaystvennyy institut i Dzhezkazganakiy
gornometaUurgicheskiy kombi-nat.
(Rhenium-AnaLysis) ((bdmes)

7 7
u3TE-I-KC , I . 1'.
11? Blireniye Skvn7hin, 3 Flroi-arvkoy "aboya Tekhnicheskoy "I Klrlbys~ev, i."rj. I-Id. ,
1954. 449. -93M. (Onift Peredovikov I.MO Ela. 65 K. -(54-g,./,?6n) r
-:62:). `45
SO: Knizlinnya, Letopis, Vol. 1, 19,;5

15-57-3-3843
Translation from: Referativnyy zhurnal, Geologiya, 1957, Nr 3,
p 193 (USSR)
AUTHORS: Fingerit, M. A., Ustenko, V. L.
TITLE: The Principles of7'*RfaTAt5ii%-'na1' 5 li~ng Programs (Osnovy
ratsional.Inykh rezhimov bureniya)
PERIODICAL: Normativ no-issled. st. pri ob"yedinenii Kuybys hevneft,
Kuybyshev, 1956, 59 pp
ABSTRACT: Bibliographic entry
Card 1/1

GAZARYAII, Artem Grigorlyevich; us,rENKO., V.L., red.1 PhTROPOLISKAYA,
l,'.Ye.,, red.; DURASOVA,~T:F,.~~,Mft-.`red.
(Our experience in the use of bydrocyolone installations]
Nash opyt primeneniia g1drotsiklonrqkh ustanovok. Kuibyshev)
Kulbyshevskoe knizhnoe izd-vo, 1962. 22 p, (MIRA 17:1)

DVORETSKIY, Arkadly Sargeyevioh; WNW, V.L., red.1 PETWPOLISKAYA,
N.Ye., red,,; DVRASOVA, red.
[Rotary turbodrilling] Turbinno-rotarnoe burenial 1z opyto
raboty tresta "Pervomaibmarneft." Kuibyshev, Kuibyshevskoe
knizhnoe izd-vo, 1962. 23 P. (MIRA 16s6)
(Oil well drilling) (Turbodrills)

Chrr,triat cgrar;h-',-: arial-~-_o
i tekh. too!. : mase I
Ktlyby~qll e v s I iy nrLu.-; Y.n, c :m a I kiy Jj -is t, !,2 f

UO-UNKO, M. S., YARNYKHP V. S.
Veterinary Medicine.
Treatment and prevention of pneumonia. Veterinarlia 29 no. 5, 1952.
9. Monthly List of Russian Accessions, Library of Congress, Agowt, 195Y.2 Unclassif led.

Uv.!Ino, V. S.
"ZostylIO an improved liquid sprayer. Vaterinariia 30 no.2:49-51
F 153. (MLRA 6:2)
1. V.sesoyuznaya nauchno-issledovatellakaya laboratorlya vatert-
narnoy sanitarii I dozinfektail Mininterstva mellskogo khozyay-
stva WM.

UST&M, Ves,., nauchny sotrudnik.
Disinfection of livestock buildings in Anjesky's disease. Yeterinariia
32 no*7:82-83 Jl 155. (ML&A 8:9)
(DISINFXCTION AND DISHMECTANTS) (PSZUDOR&BINS)

USTENKOR V.S., Cand Vet Sci -- (diss) "Disinf-,~ction of rooms and
,tanning and fur stock Iloscows 1957y 16 pp
(Mloscow Veterinary Academy) 14C copies (IM, 36-57, 106)

USTENKO, V.S.,nauchnvy notrudnik; SHAKULIN. A-A-ekand.tekhn.nauk
-,
.&I Disinfection of hides ani skins which may be carrying AU46qkyle
11. .0
disease. Trudy VNIIVSI 11:363-375 157p (KIRA 3-1:12)
(Pneudorables) (Hides and skins-Zisinfection) I

POLUKOV, A'A.; Umilzo, V.S.
, I
Spr"ers and their use. Trudy VNIIVS3 11:403-W5 '57-
(MIRA 11: 12)
(Spraying and dusting equipment)

USTINKO, T.S., nanchnyy sotrindnUc.
Viability of An-jesky's disease virus. Veterinarita. 34 no.3:74--75
Mr '57. (MLRA 10:4)
(Pseadombies vims)

USTMKO, V.S.,nauchnyy sotrudnik
Viability of the virus of Aujeek7ls disease outside of the
animal organism. Tzaiy VNIIVSI 13:49-59 158. (KIRA 11: 12
(Peaudorabies)

;i . ..
t ! ! ~ 't m i ,~ . , ~ 1 , ,
v

USTMEO 'ru-T-3 SU
pcr, ancl in alwirlum
Ajaperometr dB t-01-111 n 1-1* ro:" I
a3loys by 1writh "'fiv. lab, 50 no,60.
~62-663
. '-Cw-
1. r1hiepinpot- 'r-i 1 1 rn 1-k
F.F. Dzer7hin.,31kc,~g-'.

USTIASHVILI, A.D., prof.- TUSHISHVILI, V.M.; BAKRAME, G.A.
P
Obstetftc vacuun extractor* Akush. i gin. no.100-72 165.
(MIRA 18slO)'
1, Wedra almaherstva.i ginekologil (sav,- prof. A.D,
Untiashvili) pediatrichaskogo i sanitarno-giglyanicheskogo
fakullteta Tbilieskogo melditsinskogo instituta,

USTIMST.711; A. 1).
22767 Untic:-~YvIlij A.
cro i i ic op,. H-7)) z- yr:z'
c ITa ~WS. "az.
zlllm -
JQIQ
so: letonis, ) No. '107

USTIASHVILI, Aleksey Dmitriyevich
[Blood transfusion and the Rhesus factor in obstetrics
. and gynecology] (Perelivanie krovi i rezus-faktor v
ak-4-3herstve-ginekologii. Tbilisi, Sabehota Sakartvelol
1965. 135 p. [1n Georgian] (I.IIRA 18:8)