SCIENTIFIC ABSTRACT ANDREYEVA,I.B. - ANDREYEVA, I. Y.

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CIA-RDP86-00513R000101410002-2
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S
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December 31, 1967
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SCIENCEAB
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The Results of Seismic-Aooustic Expluration 2o-119-3-52/65 of the Bottom of the Japan Sea depth of loo-6oo m. 2 pairs of Kpaographs directed opposite (vatrechnyy) to each other were constructed from the data on the entering of refracted waves and data on the limit velocity of the sound as well as on the depth of the refracting boundaries of the deeper -seated ground la3ers. 2 layers with considerably diffe- rent limit velocities in both cross sections could be distinguishud. The velocities differed in both cross sections. This difference seems to be due to measurinb. errors and to the fact that the actual geological cona ditions did not agree with the idealized assumptions the computation-was based on. Apparently a basaltic layer of a thickness of from 6-7 to 7-8 m is stratified under the loose deposit. As it seems to the authors the results prove the fact that a considerable mass of loose ground deposits exists in the western part of the Ya- ponskoye sea which is not separated by distinct boun. daries. The change of ihe thickness of this layer is obviously connected with the supply of deposits from Card 3/4 the continent and with the relief of the subjacent ANDREYEVAOI.B.: LISITSYN.,A.P.: lUD:INTSEVO G.B.: NEFROCHNOVIYU.P.: SYSCIEV,N.N.: )ITIC101#11M, I.)M. "Results of Seismo-Acoustic Irmestigations of the Ocean Bottom" 31-AUG 11 Sep 59 a paper presented at the international oceanographic congress , 31 aug--=e) ~9 -IL/ , A: w Yo ,C < so; 73, 3, 142)129 22 )ct 59 FRASE I BOOK F-17LOITATIM SOV/5331 International Geological Congress. 21st, Copenhagen, 1960. X*rskaya goc2oglya (Iffarlme Ooology) Moscow, Itd-vo AN 3.%Mns 1960. 205 p. 2,500 copies printed. (3erleas Dok2ady movetakLkh geologoTs problema 10) Zd1torial Boards P. L. bezrukuys Reap. Ed.; A. V. 2hivaZo. V. P. Zenkovich and 0. B. Vdintsev; Ed. of Publiching Uouses V. S. Sheynstan; Tech. Zd.s V. Karpov. PURPOSEt Oda book is Intended for goo2ogisto and oceanographers. COVERAdRs The book contains IS articles representing the roporto given by Soviet goologlets at the 2lot. International GooloCleal Congress. Individual articles deal with the bott4m tc*aZr.-Ay. sedimentation, and t,"tonlea of oceans (W:5torn Facifto and Southern Indian), to well an the Zoomor2holoZj and tectonics of the Black and Conplass Benz and Soviet sectors of the Baltic. An 7-01-h rdo=* accopDassise oach article. No personalities X. W., I. Y.*. my-hax-t,eq!, 0. a. llcitz7n, and J~. 1. Xoproclpv. 7FCR%Llto Of tions -tfi--UiW a Crust Under ountitSURG f a Seas and Oceans 35 ftldov~ Sh K. StratIgraphi -Cf'Sediment.~ and the YaleorecCrs;4hy OrtH. j.r torn Pacific and the Far Zr3tarn Seas of the USSR According to Sea-Dottom Foraminifers 59 Formation of Sediments in the Southern -Pacific and Indian Oceans 69 laplbj.-JE.P~.. and X. A Belay. Bottom Sedimentation Can. M-no in ihe Are can 1 88 a t1V.PP_ and TO. F. Xpro6mov. Bottom aeactorphology o-nMdUctatov. robleass of the black Sea 94 0 " V. V;' L 3 Mdakova and 0. V. A Relief and HOMMAYP-31 ruVt~u;;. 105 Re on r M GerahanovIch D To Recent Shelf Depoolta in the X4xg1nv2 of.11W tn;x- Seas 1& 116 a, The Oeo2ogr of the Barents Sea 123 Gorahkova, T. 1. Sediments In the Norwegian Sea 132 V. Study of the Diagenessiss of Some Marine 140 Zenkovich V F , 0 K Leontlyevp and To. it V vessak:y. The -influence or &6irF-fo -ulaclal Tranc~Fosla n r4w Development or the Coastal Zone of Soviet SeLs 154 bulatov, X. A., V. L @v and V 7 ZonkovIah. go" l64 Budanov, V. Ii. A; 1. loan, 21n, and V. 3. Modvedev. -4W" f the 8Zft6f-U=UrT- IT5 -He , Vert 0 1 vemsenta 0 Be orea jXSv,0. X. Types and Formation of Lagoons a" Recent 3.29hores- IBU Card-VJ& ANDREYEVA, I.B.; CHINDONOVA, Yu.G. - - Nature of sound-scattering layers. Okeanologiia 4 no.IsII2-124 164, (MIRA 17:4) 1. Akustichoskiy institut AN SSSR. ANDREYYEVA, I.B. 1. Z-3cattering of sound by fish bladders in deep Bcattering layers in the ocean. Akust. zhur. 10 no.ls20-24 164. (MIRA 17:5) 1. Akusticheskiy institut AN SSSR, Moskva. t W(lVkW( _iAid'(0-4: lk TJP 0 W/M ACC Mi AP6011944 SOURCE CODE: UIVO2131651005100611-MA 07 AUTHM Androyqva 1. N ORG:. Acoustics Institq~.j_hj~SSS& (Akusticheakiy institut AN SM) TITLE: At,,-austic-characteristies of sound-scattering layers in the ocean and data 4~ of echo ounder observations anT-direct catches SOURCE: Okeanologiya, v. 5, no. 6, 1965, 1028-1037 ~TOPIC TAGS: acoustic scattering- acoustic wave,-ocean acoustics, sonar ABSTRACT; In order to take into accourit-~he influence of sound-scattering layers on the pr9pagition of acoiistic waves In the ocean it is necessary to Mow their quantitative acoustic characteristics: intensity of the layerp scattering coefficient and the depend,,;.-.ce of these parameters on frequencr and depth. Data from echosounder observations can be ex- t re. onalization of lage ocean mely effective both for a preliminary regi -areas on the basis of the abundance of sound-scattering accumulations ,and for faci2-itating the regionalization made on the basis of the results of quantitative acountic measurements. Hodern echo sounders, designed. '.1 for measuring ocean depths, cannot ensure measurement of the cluantitative''I characteristics of sound-scattering layers ana therefore do not make .poss-iblo even qualitative bvaluation of the degree and character or the 'influence of biological accumulations on the underwater propagation of -sound. Relatively small changes and additions to depth sounder circuits.,,- L_ Card 1& UDC: 577-472(26) L 4b956-66 egl~j ACC NRs AP603045( SOURCE CODE: UR/0213/66/oo6/oo4/o599/o6O7 AUTHOR: Andreveva. I. B. ORG: Acoustic Institute (Akusticheskiy institut) \V TITLE: Study of volume sound scattering in the ocean and measurement of acoustic characteristics of scattering layers SOURCE: Okeemologiya, v. 6, no. 4, 1966, 599-607 TOPIC TAGS: acoustic scattering, acoustic detection, acoustic analysis, sbipborne, acoustic detection, acoustic equipment, acoustic measurement, acoustic propagation, underwater explosion, underwater acoustics, underwater sound equipment, ocean acoustics, oceanography, volume sound scattering ABSTRACT: The article describes the development and use of modifications of a method of measuring the averaged acoustic characteristics of both the sound-scattering and.~h surface-bubbling layers. Two types of experiments (see Figs. 1 and 2) were under- taken to determine the characteristics of volume scattering. Two formulas are giveR-, which serve as the initial computational relationships used in processing the experf4 mental data. The procedures followed in both experiments are outlined in detail, and the methods and equipment used,in recording and processing shot data are described. Two steps are followed in analyzing the experimental data. The first consists of frequency selection with the output re-recorded on magnetic tape. The primary Card I/q UDC: 551.463.262(26) C"d.. Zt3- L 46956-66 ACC NR, AP603t)456 (I V -, 4 4i e~~~er Fig. 1. Setup of components in'- experiment 1 1 - Recording mid control system; 2 - weight; 3 - hydrophone and preamplifier; 4 - shot. . layer Fig. 2. Setup of''compone'nit's in experiment 2 1 - Recording and control system; 2 - preamplifier; 3 - hydrophone; 4 - charges; 5 - weight; 6 - shot. recording of each shot is filtered 8 to 10 times. In the second step, the secondary recording is reproduced, amplified,.and detected. Using formulas given in the article L- 4695 ACC AP603o456 3 and the detector outDut signal, scattering strength and the dependence of the scattering coefficient on depth may be calculated mwiu&lly or by computer.* The assistance of I. Ye. Mikhalltsev, Yu. Yu. Zhitkovskiy, and B. F. Kurlyanoy in developing the deacribed technique is acknowledged. Orig. art. has: 12 formulas and 6 figures. [LBI SUB CODE: 08, 17, 19, 20/ SUBM DATE: 17ju165/ ORIG REF: oo6/ OTH REF: 0o8/ ATD PRESS: 5088 Card 3/3 ACC NRt jIF7000141 -~66i&i~-c-oi~i-.-6ii6-o-46/66/0'1'2-/00'4/-039~/o o4. ;'.AUTHOR: ~~l!!Xyj~k,I,..,,B.";,-Kharatlyan, Ye. G. I-ORG: A*C-0*'Ustic natitute, AN GSBR, Moscow (Akusticheakiy institut AN SSSR) TITLE: Sound sdattering by the ocean surface and by near-surface sound-scattering layers iSOURCE: Akusticheakiy zht!- -nal, v. 12, no. 4, 1966, 399-ho4 TOPIC TAGS: scattering, aaand . grazing angle, oceanAPeG%%rP6u%,, acoustic scLttering The resultj of af .-,;,.,stigation ol- sound scattering by' the near,rface layers u of !:'he oce~v by the resea.-..h vessel "Hikhail Lomonosov" in the Vist.ern e-j4at,,!.-.. rrigion of the Atl.~MtiC Ocean in September--Noverber 1963 art- described. Underwater explosioA-i served as acoustic sources, while a c,.--.-qic sphere locate4 a short disttAce above them point of explosion was the hydrophone.1 The depth of the wholf system was varied between 200 and 500 m. The absolute values of the effectivo surface backscattering coefficients (a) were dateralined from the recorded scattering. The frequency dependence of a as well as [its variation with the grazing angle were also obtained within the limits 'of 1-40 ke and 10-60', respectively. It was established that at Card 1/2 _Vw; 534-24:551-46 ACC NRI APWOK~hl grazing an es 688 than 30' and at frequencies of 3-10 kc, the scattering field is termined primarily by volum scattering and not by scattering by 'Ifttif nonhopogen ities of the air-water interface. At grazing angles greater than 30* and at frequencies of 1-2 ke and 10-40 cps, scattering is believed to be caused 1by surface nonhomogeneities. Orig. art.. has: * 6 fomulas and' 4 figures.! suB-com oe/ huBm DATE: O1jun65/ ORIG REF: 006/ M REF: OOT/ An PRESS: 5112 Lcqrd 2/2 s/i86/63/005/001/007/013 E075/E436 AUTHORS: I. B. Andreyov, P.P., Rogozina, E.M. TITLE: Investigation of the processes and interaction products of high molecular weight compounds with inorganic salts II. Formation of complexes between poly (a-methyl)acrolein and uranyl nitrate PERIODICAL: Radiokhimiya, v-5, no.1, 1963, 103-1o6 ,TEXT: Polymerization of (a-methyl)acrolein was carried out with different catalysts to investigate the influence of substituents in the a position on "be ability of the polymer to complex with U02(NO3)2- Ethyl-, propyl- and butyl-acroleins were also synthesized but could only be polymerized with metallic Na. Details of the polymerization procedures will be reported separately. Poly(a-methyl)acroleins obtained by emulsion :.polymerization with AgN03 and K2SO5 Mohr's salt and K2SO5, 6 hyposulfite and K2SO5.absorbed 1000 x 10- go U per g of polymer. Auto-polymerized polymer absorbed 2000 x 10-9 g of U per g of polymer, its content of aldehyde groups being of the same order (66 to 69 mo.1%) as in the previous polymers. The polymers Card 1/2 s/i86/63/005/001/007/013 Investigation of the processes ... E075/E436 obtained in the presence of BF3, lithium-butyl and Na contained only 9 to 12% aldehyde groups and did not complex with U. The. complex formation took place to the greatest extent at the pil values of 3 to 4. In general the presence of inethyl gr-)ups in the polyiner makes it hydrophobic and less capable of complexing with U than polyacrololn. There are I figure and 1 table. SUBMITTED: January 3, 1962 Card 2/2 ANDREYEVA I. F. I ZUBKOVICH, L.E. =L~- 19856 ANDREYEWVA, I. F. i ZUBKOVICHp L. E., Svoystva karbogidraz v sozrevayushehem zeme pshenitsy i sintez krakhmalInykh zeren vne zhevoy kletad. Biokhemiya, 1949,, Vyp- 3, s. 249-55. -Bibllogr: 7 nazv. SO: LETOPIS ZHURNAL STATEY, Vol. 27, MOSKVA, 1949. ANDREYEVA, I.I. Rhythm of the seasonal developmant of plants in the mixed beeoh and chestnut forests of the Batum seashore of the Caucasus. Biul. Glav. bot. sada no.51%67-77 163. (MA 17:2) ?c 3dagogicheskiy institut imemi Lenina, Moskva. ANDRNYEVA, I.I. Shoot formation and the rhythm of seasonal development of the same species in Moscow Province and on the Butum shore. Biul. Glav. bot. sada no-54:9-16 164. (MIRA 17:11) It Moskovokiy gosudarstvennyY pedagogichaskiy institut imeni Lenina. SOURGH CODSt 66o/bl3/bo5q/0O5O ACC NR, Ap60j560� f4 To~~1661 DWIMORSt Volkov) So No; Makarlinp Vo Poj Falevich, K. X.; Rubaylo, G. ft.; Gorasimova,j~._4,j Fqazantaeva, Vs Mq Andrey Semenova, A* Go ORGi none TITLE; A machine for contact spot welding. Mass 21p No. 183300 SOURCE: Izobrateniyas pronyahlennge obraztey, toyarnyye znaki, no. 13) 1966, 50 TOPIC-TAGS: welding, spot welding, welding technolo y, welding equipment ABSTRAM This Author Certificate presents a machine for contact spot welding. 'the machine contains a frame and welding transformers, each of which is electrically connected to a group of welding guns (see Figo I)o To increase the productivity, the welding transformers together with.the corresponding group of welding guns are mounted on the vertical planes of plates which move under the action of a driving mechanism located on the frame. The movement takes place along the horizontal guides also located on the frameo Rods attached to one of the plates serve as auxiliary pides for awther plate. These rods are intended for fixing the plates Card 1/2 I=t 421-701-M.I.nT ACC Fig. 1e I - welding transformeraj 2 - welding gunn 3 wA 4 - vertical"platsai - driving machanim for plates; 6 fr"ej 7 - guides; rod* in their original posit..-. -_-7.~or to w&Uingo. OrIS6 arU hass I figure. S" CODII 231 SM DVI# 16hrAS ANDREYETA, I.M.,; IVANOV, I.T. Use of semiconductor diodes for electric frequency control in oup6rbigh-frequenoy cavity resonators. Vest.Mosk,,un. Serjt Fiz.,,astron. 17 no.613-6 N-D 162. (MIRA 15a12) 1. Kafedra teorii kolebaniy Hoskovskogo universiteta. (Electric resonators) (Diodes) ALEKSANDROVA, L.N,; ANDRMVA, I.M. Transformation of humus substances in the soil. Pochvovedanie nc).7:20-26 JI '63, (MIRA 164) 1. Leningradskiy sellskokh-ozyaystveWi5,y institut. (Humus) w KAGAN, D.F., kand. tekhn.nauk; VANYAXIN, D.M., kand. tolckn, nank; LOUCREV; F.V., kand, tekhn. nauk; YEKNUKOV, S.V., inzh.j PAVLOV, L.D., inzh.; RUZINq M.Yn,., inzh.; ANDMEVA, I.N., inzh.; SHMOVA, G.D... inzh. Prininali Mucga~stiye. SAPOZENIKOV, M.M.j kand. tekhn. nauk; GEFDING, A.K., kand. teklm. nauk; MAUIOVSKIY, H.B.p inzh.; STRASWO, V.P.p red. izd-va; W3MOV, D.Ya.s tekhn. red, [Instructions for designing, installing, operating, and repairing interior water supply systems using vinyl plastic pipes) Ukazaniia po proektirovaniiu,, wontazhu, ekspluatatsii i remontu vnutrennikh vodoprovodov iz viniplastovykh trub. Moekva; Goa. izd-vo lit-ry po stroit., arkhit. i stroit. mi- terialam, 1961. 91 p. (MIRA .15.-2) 1. Akademiya stroitel'stva i arkhitektury SSSR. Institut sa- ni-FArnoy tekhniki. 2. Nauchno-isoledovatellskiy institut sa- nitarnoy tekhniki Akademii stroitel'stva i arkhitektury SSSR (for Kagan, Vanyakin, Lobachev, Yekhlakov, Pavlov, Ruzin, Androyeva., Shmakova). 3. Leningradskiy nauchno-iB'sledovatellaidy institut AAademiJ kommunallnogo khozyaystva in. K.D.Pamfilava (for Sapozhnikov). 4. Vaegoyuznyy nauohno-insledovatel'okly in- stitut gidrotakhnichoskikh i qanitarno-tekhnicheskikb rabot (for Gefding). 5, Institut po proyektirovaniyu zbilisholmo- grazhdanskogo stroitel'stva V.5. MoDkve (for Malinovskiy). (Water..pipe . -IT- A~ --I ANDREMNA, 1. N. "Detemination of Gonstan-~s of the Vigration of a Chain of Organic Compounds in the Initiated PolynierizatJon of !b-thyl Metacrylate." Min Higher Education USSR. Leningrad ()rder of Labor Red Banner 7echnological In:31,-, imeni Leningrad Soviet. Chair of the 'reclinology of Plastics. Leningrad, 1955. (Dissertation for the Derrme of Candidate in Chemical Sciences) SOURCE Kn1zhnaya Letopis', 'mo 6 1956 AM 0 R E'Y F- Y141 ~T-, 1Y, YEGOROV, N.Me; AMIPOVA, Z.V.; VBSBWVSKAYA,, Yaj.; IJCVINA, A.A.; SIMOTA, A.&,;.3MAVSKIY, A.Ge; ADMITIVAg I*N* Gyalic and continuous methods for the polymerization of ethylene at low.pressures.-Khim. nauka i prom. 2 no-3098-399 157, -- _i I" iy ins' WRA. 10:8) 1. Hauchno-iseledovate sk titut polimerizatsionnykh plastuass, (Ithylens (Pblymerization)~ RtORF-YEVA, I-W 50) P. PHASE I BOOK ECEWITATION SM11639 Polietilen nizkogo dayleni" (Im-~resoure'Plolqethylene) laningrad Goskfilmizdat,, 1958, 90 p. (Series: Novyye plastichepkiye mwly~ 10,0W copies printed. Ed. (Title page)- N.M. Yegorov; Ed, (Inside book)t Ye. T. Shur; ., Tech. Ed.: Ye. Ye. Irlikh. PW.1039: This booklet is intended for sechanicii engineers and 1,echnicians in chemistry., petroleizm technology, foods., pharmaceuticals, electrical enginearingi, battery manufacturing, radio engineering, automobile manufacturing, - hifilb;; . frequency engineering, televisions ommmicationss machine- and ihiV-bftild1ngp aviation, construction and other branches of industry empioying plastic materials. COVERAW: Thar booklet deseribes a nev mater:L4.- polyethyle.ne-produced at low pressures. ' Its industrial preparation and properties are deseribed along with rbethods of taking articles from this material and its application in building technology, medicine and other branches of science, The booklet vas compiled by personnel of the Scientific Research Institute for Polymerized Plastics., Ch. I.: I.11. Andreyeva, Z.V. Arkhtpovs, Ye,V. Veselovskaya, AA, JAvina; CardlA I.ow-pressure, Polyethylene sov/1639 Resistivity and electric strength Aging of low-pressure polyethylene 30 Ch. III. Manufacture of Polyethylene Articles and Their Fields of Application 55 Die caiting 50 Extrusion method of processing 61 Coating of conductors with polyethylene insulation 70 Processing low-pressure polyethylene by press forming 71 Applying protective coatings of low-pressure polyethylene to metal parts by fusion 76 Welding plates and pipes of low-pressure polyethylene and the formation of sheets (bending operations) 77 Welding sheets and plates 78 Welding pipes and welding-on flanges 80 Making T-Joints by velding pipes at right angles 83 length-irise weldiT* of tubing from sheets of low-pressure polyethylene for ventilation and other purposes 84 ]L-ndbg low-pressure polyethylene sheets and plates to a given angle 86 Welding low-pressure polyethylene parts with a rod and employing a stream of hot air or nitrogen 87 Card 3/4 ANMN"74 A,LII.-;-ARKHIPOVA. Z.V.; VASSLOVSEAYA, Ye.Y.; UVINA, A.A.; ANTOKOLISKAYA, U.N.; LAZAREVA, K.P.; SAMIN, B.I.; KRINIKIS, S.S.; SHCHEREAK, P.H.; GERBILISKIY, I.S.; LYANDZMG, G.Ya.; PARMORKOVA, T.V.; PHOHERKIN, A.L.; INGOROV, Y.M., red.; MM, Ye.I., red.; POMKINA, T.A.. tekhn.red. [Lov-pressure polyethylene] rolietilen nizkogo davleniia. Izd.2.& lepr. i dop. Leningrad, Goe.nauchno-tekhn.izd-vo khim.lit-ry. 1960. 95 p. (MIRA 14.-1) 1. Nauchno-issledovatel'skiy inatitut polimeri2atsionnykh plast- mass (for all, except Yegorov, Shur, Pomkina). ('Pol~athylene) EWT(z)/9PF(c)/EWP(J)j;~1' RPL W)~M M L 3913,- AP5024496 UR/0191/651000101010OQ4/0006 ACCMSION NR: 4'~' ~< 678. 742. 2-134. 24:678. 044:547. 419A N. Z able AUTHOP- An_dreyeva. tual, V, ---M Seyergvg. N. v, 7 7 V t1 Cq' 'iihylene (with p #nTLV WlXnerizalt6n using certain 6rgat-omkill catalysto SOURCE: Plasticheskiye massy, no. 10, 1965, 4-6 'a TOPICTAGS- ethylene, propylene, copolymerization, catalytic polymerization, polymerization rate, copoly,::aer, polymerization catalyst, organoaluminum com-~,, pound ADMIACT: The relative activity of ethylent~- and propylene in their copolymeriii y s' tion using Ziegler;-NattaS died to obtain data necessary for the, 1~as Stu. -%Ljl Sts t ve perties. The rela i production of copolymers. having valuable technical p,~d, activity. of propylene during copolymer-1 zation w1t4.0ift~:re6t ~,aialyst.sy~teMs' i~~ creased Inj-he folloviing;-Order. + TIC14; (2~Al( (1) AUCA )2Cl C2lI5)3.+ TIM 5 1 . 4 (3) A1(C2H -13 + VOC13-; (4) Al(C H5)2C1 +V. -=13; and, (5) AI(C2"5)3 + IX -TiCl 5 2 30: Change In catalyst concentration had no effect on the activity of the monomers. hange in the ratio of catalyst components in catalysts (4) and (5) did not chealge Card 1/2 17 L 3912-66 - ACCESSION NR, AP5024496, the composition of the copolymer, but decrease in the ratio of the aluminum alkyl in the other catalyst systems led to an increase in the propylene content in the copolymer made with catalysts (1) and (2), and a decrease in propylene when us-. ing catalyst (3). The copolymerization constants have the same values when ca- talyst systems (4) or (5) ar6 used or when the Al(C6Hl3)3 + K -TiC13 system is used, indicating that different'aluminum alkyl derivatives in combination with V - TiC13 do not change the. relative activity of the monomers. Thecopolymeriza tion constants change significantly with a change in the aluminum organic deriva-_ tives in systems based on Tidl4, This Is apparently due to the different reductf- vility of the aluminum, organic derivatives and subsequent formation of different-., active centers. Orill. art. htis., 2 tables, 1 figure and 2 equations. ASSOCIATION: None SUBMITTED: 00 ENCL: 00 SUB CODE! OCI MT SOV.- 002-._,.~" '_ -0 ER. 004 t '14 i? Car 2 7 AIZA 4WEM OMIN 7 -7:- -'R-PT.; Ww vu PR: ~j -TrXLE: of an eZhyleni propylene tqp_OU_~ mer uw- 1965 9' 127, Pra-st, C 11AUye iWSSy0_A a- c0 yme -s 'thesis- -'poly TOPIC TAGS -pihilene: cdp~lymer. 'POI. rp~ _,:,V;c?pyie-n polyolefin: yn mer structure, p6lydi3persity, Zieglir.catalyst, polymer fractionation, Polymer -molecular- weight f--- --- --in the-presenm-o a p~hne' fii d- '_ABSEVRACre. -Ethylitne. -_-ware_6olution~p yme a n to aw-dy- the molecular weight distribution, COM o ition~ Ziegler-catalystj order - I P 8 and intrinsic vi6covity ofthe.copolymer and the mutual effects of molecular weight and viscosity. The monamers were polymerized at 4-5 atm. with triethyla- luminum-titanium tetrachloridet'o form a copolymer containing 4-10 mol.% propy-I- lene, determined ' apectrographically from the methyl group concentrations. The intrinsic viscosity was mangured in decalin solution on a capillary viscome- ter- at 135C, the weight -average molecular weight was'datermined with an optical 77 ------ ------ -44 0 C ------------ 4t- j tj J"01-~ellt aj~~-t tkilin h- ti ion wi to that of low pressure--P0 by precipitat to be a imilar jar weight distribution va own. ctoril- by Tung's distribution functions ethylene and to be described satisfa 7 molecular weight of the fractio Wourn. Polymer Science v. 241,19.57, 333). The ns decreased with increasing.content of propylene links. Fractionation was t;hown to proceed both by copolymer Icomposition -and by molecular weight. The studied did-not _indtcate a dii Ict de-efidence-of molecular weight-on intrinsic'. --specimen e p _isoodity,,--and --latte -,ParoLmetAi~is.,nof---recommenied for determining tile mole -+ v lar in this ty e:, of ~~opqjymer'#-. Or S'., ar u -weight c I ASSOCIATION,: :., vone Zj 06 JD_ 9 .00 SUEHMED 4t OTMt 005 77 - No REv-sovi -003 7, - J M4 V4 -ACC NR, A1'6(i2~65~- F-uft/o4l3-/6-6/o,)o/014/0050/0081 INVENTORS: Kuznetsov, Y06 Vs; Gusev, V. I.; Zhi4kova, T. N.1 Andreyeva, I. no; Somenovap L. S.. ORG; none TITLE: A motaod for obtaWng copolymers of propyleno. 01ass 39, No. 183938 SgtJR(;E-. Izobret prom obraz tov zn, no. lh, 1966, 60-81 TOPIC TAGSt polyiner,, copolymer, propylone, polyinerization, ester, phosphoric acid., catalyst, titanium compound, compound ABSTRACT: This Author Certificate presents a ~.~Dhod for obtaining copolymers of propylene with unsaturated compounds in the medium of an inert carbonaceous solvent at the temperature from 20 to 60C. The process is carried out in the presence of a catalyst consisting of titanipm tetrachloride and aluminum alkyls. To impart the property of fire resistance to the copolymers, unsaturated mixed esters of phosphoric acid are used as the unsaturated compounds, SUB CODE: ll/ SUB14 DATE: 06Sep62 0 UDC.- 678. ANDREYEVA, I.N.I,ZAPLETNYAK, V.M.1 SEVEROVA, N.N.; ARKHIPOVA, Z.V. Copolymerization of ethylene and propylene with the use of some organometallie catalysts. Plast. massy no.10:4-6 165. (MIRA 18:10) 1. Ti. GINULI, ?.A.; ANDREVIVA, I.N.; YXMAKOVA, K.G.; TSVrGTKOVA, Xffect CT the-newti'llage system on the basic features in the physiology of wheat* Isy. AN SSSR. Ser.biol. no.4:44V465 Jl-Ag '57- (KLRA 10:8) 1. Institut fisiologii rastenty Im, I.A.Timiryateva Akedemit nauk SSSR. (TIIJAGB) (WHIIAT) AOFI~'VA.p I.N. Plant nutrition as influenced by T.S. Malitsev's new tillage system [with summary In ftlighl, liziol. rast. 4 no.6.'533-541 X-D 157. (MIRA lOt12) 1, Institut fitiologii rasteniy Im. K.A. Timiryazeva AN SSSR. Xoskva. (Tillage) (Plants--Nutrition) NDREyEvA, _IL-,-Oand Biol Svi (dies) "Peculiarities of nutrition A 41 of plants unde r now system of treatment of soil. fteovvA -ing-066 W-e-T Physio I"al-tsev jVt%WpO 1joa, 1958.. 20 pp (Inst oi logy of Plante im K. A. Timiryazev, Pcaa Sci USSR), 150 copies (KL, 13-58, 106) -/F- OMTRY USSR CAT3XVRY Plant Physiology. Mineral Ilutrition. B5. JOUR.~ i RM161.0 No. 6 ~959,o No- 24533 : Andreyeva, 1.11. S - TITLE Gharagteristios of Plant Nutrition Under the New r;yatem of Soil Wtivation of T. S. Malltsev OZG- PUB-- t P1ziol-.rast6ni7-q 19571 4, No. 6t 533-541 BSTRACT t In fields on the collective farm "Zavat Illichall and in the Shadrinskiy Rayon experimental station of. Mrganekeya oblesti, for the purpose of soientifioally testing the new system of soil cultivation of To So Valltser I a system of mineral nutrition of corn and sunflower vms studied by determining the composition of the plant juices by the Sabinin method (Biol. otd. semled., 1928, No. 15). It has been established that the method of diagnosing mineral nutrition by analysis of the 1/2 11 GENKELI, P.A., prof.; ANDREYEVA,..1 ., kand.biologicheakikh nauk "j( Now scientific data on cellular structure. Biol.v shkole no.6t83-88 N-D 162. (MIRA 16W 1. Institut fisiologii rastenly imeni K.A*Timiz7azfva AN SWR. (COUS) (Electron microscopy) ANDREYEVA, I.N. Absorption of mineral substances by plants subjected to a desiccant wind. Fiziol. rast. 11 no.1:79-86 Ja-F 164. (MIRA' 17:2) 1. Institut fiziologii rasteniy imeni K.A. Timiryazeva AN SSSR, Moskva. Oxidative phoophor-y3Ation in the mitochondria Fiziol.rast. 12 no-4215,84-590 JI-Ag 165,, 1. Institut fiziologit Moskva. Submitted June (MIRA 1802) K.A.Timiryazeva AN SSSR, A1TD1--ZF%VA-)- - I.- - P.- nInvestigation of Irregular Operation of Hydroelectric Station Aggregates." M;scow Order of Lenin Power Engineering Inst imeni V. M. Molotov, Min Higher Education USSR, Moscow, 1955. (KL, No 14, Apr 55) SO: Sum. No. 704, 2 Nov 55 - Survey of Scientific and Technical Dissertations Defended at USSR Higher Ed-ccational Institutions (16). -F, W- ANDRUIVA, I.P., kandidat takhnichaskikh nauk, StalAlity of steady states in hydroelectric power stations and power systems. Tr*r NEI no.19:95-105 156. (MIRA IM-1) 1. Xafe&ra gidroonergetiki. (Pbwer engineering) TV ANDRMTVA, 1. S. - "Anatomiconorphological and Biochanical Character of Pears with Different Rates of Ripening." Cand Agr Sci, Fruit and Vegetable Inst imeni 1. V. Michurin, Min Higher Education USSR, Michurinsk, 1954. (KLI 140 17, Apr 55) SO: Sum. No. 704, 2 Nov 55 - Survey of Scientific and Tec1mical Dissertations Defended at USSR Higher Educational Institutions (16). ANDRrMA, I.S., kand.sel'ekokhozyaystvannykh nauk The ability of pear to take root from green cuttings. AgrobiologRa no.1:146-147 Ja-F 159. (MIRA 12:4) 1. Baratovskly sellskokhosysystvenzily institut. Mari ANDREMA.. I.S. Anatomic structure of Acanthopanax sessiliflorum Seem. Soob. MAN SSSR no.18s67-72 163. (MIRA 17:11) 1. Dallnerostochnyy filial imeni Komarova Sibirskogo otdeleniya AN SSSR. ANDREYEVA I S Anatomical characteristics of ginseng roots of various age. Mat. k izuch. zhen'shenia, i lim. no-4:216-M 160. (MIRA 13:9) 1. DallnevostochM filial Sibirskogo otdelaniya AN SSSR. (GINsENQ (ROOTS (BOTANY)-4HATOMY) ANMYEVA Comparative microohomioal study of plarits of the ginseng famJ17 in the Far East. Mat. k izuoh. zhen'shenia i lim.,no.4t222-224 160. (MIRA 13:9) 1. Dalinevostoohnyy filial Sibirskogo otdeleniya, AN SSSR. (SOVIET FAR EAST-GINSENG) (GLYCOSID.&S) .-ANDREYEVA, I.S. Some anatomical characteristics of Eleutherococcus sentioocus Bax. Soob.DVFAN SSSR no. 15:135-138 162. (PIRA DO) 1. Dallnevostochnyy filial Sibirskogo otdelenlya AN SSSR. ISAYEVA, Z.G.; An_ Int'eraction of 4 3 -carene oxide-with.methyl alcohQl.in the -prenance-of-sodium methylate. ..Dokl. AN SSSR 152 no.2-34-2- 345.S 163. (kRA 16 M) 1. Nauchno-:Lsaledovateliskiy kbimiche-skiy institut im.A.M.Butlerova pri Kazanskom gosudarstvennom universiteteim. VJ. Ullyanova- Lenina. Predstavleno akademikom B.A. Arbuzovym. ISAYEVA, Z.G.; ANDREYEVA,_I.-S. Isomerization of 4 3 -carene oxide in the reaction with alcohols in the presence of acids. Dokl. AN SSSR 152 no.1:106-109 S 163. (MIRA 160) 1. Nauchno-issledovateltakiy khimichaskiy institut im. A.M.Butlerova Kazanskogo gosudarstvennogo universiteta. im. Ullyanova-lanina. Predstavleno akademikom B.A.Arbuzovym. (Carene) (Alcohols) (Isomerization) ANDREYEVA, I.S. Dynamics of the reserve substances of ginseng during the vege- tative period. Hat. k izuch. zhen'. i drug. 2ek. rast. Dal'. Vost, no.5W-52 163. Anatomic and microchemical characterittics of the roots of ginro4g, from distant regions. lbid.t63-67 (MIRA 170) 1. Pallnevestt-chayy f1lia-I Iment Xomarova Sibirakogo otdoleniya AN &SM. ARBUZOV, B.A.; ISAYEVA, Z.G.; AIIDREYF.VA, I.S. Isomerization of OL-pinene and,43-carene oxides with lithium di- ethylamine. Izv. AN SSSR. Ser. khim. no.5:838-843 165. (MIRA 18:5) 1. Nauohno-issledovateltakiy khimicheakiy institut im. A.M.Butlerova Kazanskogo gosudarstvannogo universiteta im. V.I.Ullyanova-Lenina. -) -T.---T. - - - - -- --- - --- -- - 1420 Tasladova.lye napr-yazhennly v tallindrakh UldravItcheskikh pressov. M., 1954 8 a. 19 sm. (M-vo vyssh. obrAzovaniya SSSR. Moak. stankoinstrum. In-t im. I. V. Stalina). 100 ekz. Bespl. -(54-53768) SO: Knizhaya Letopis', Vol. 1, 1955 77- 520-4 ~: I - -(z)/EWP _HH-_ rA - ~56 W ACC_kks_' AP6001658 SOURGE CODE3 UHTow_07g;w~/O-i2 2039/2047~ AUTHORSt Kot6n. M. H.j. reveyg. 11 V Getmanchuk. )L~U P.; ttadMkaYaj_L.'YaL1 Pokrovskiy, Ye. I.; Ko ItSov, A. 1.sjxl~mbovat V. A. ORG: Institute of Huh-Molecular Polymers AN SM (Institut vysokomolakulyarnYkh, soyed Y AN SSSR) TITLEt Structure of nethacroleintpolymeraj obtained in the presence of anionic cataly;0tv, 3rd rep.ort--i'on-tl-i-e-,rer-ie~i~Polyuierization of Acrolein and Its Derivatives SOUR~Et Vysokomolokulyarnyye soyedineniya., Y. 7. no. 12, 1965, 2039-2041 TOPIC TAGSt polymerization, polymer structure,, reaction machanism, caW-,'y stl Nippon Bunko infrared spectrophotometer DS 301) GNM 3 nuclear magnetic resonance.spectrometer ABSTRAM The structure of.polymers obtained from methacrolein and 6( -ethyla~crolein in the presence of sodium naphthalene and sodium trityl -Asing the method described by M. M. Koton, 1. V. Andreyevai and Yu. P. Getmanchuk (Dokl. AN SSSR, 155, 836,~ 1964 was investigated. -The structure analysis was performed by chemical meanst~, oxime formation. hydrogenation, 9xidation with perbenzoic, acid,, ozonization, as well as physical meanst infrared spectra, using Nippon-Bunko spectrophotometer DS-301, and NMR spectra, using instrument GNM-3, It was established that the rate of conversion of methacrolein &nd the structure of the obtained polymer are both functions of the qj~ polymerization tsVzi-ature, as illustrated in Fig. 1e Mechanism of the polymerizatibn I Card L113 UDCa 678-01t53+67 0744 L 13082-66 HW(m)1EWP(J)1T Hff ACC NR: AP6002215 SOURCE COM UR/0080/65/038/012/2740/2744~ iAUTHOR: Andreyeva, I. Yjs KQto ~nM. ~M. GqtmancbA;k Tarasova, IORG: Institute of High Molecular Compounds, AN SSSR (Institut vysckomo1.ekulyArnY 'soedinenTy-ANSSSR) IVA TITLE: Emulsion riz -pol atio of methacrolein iSOURCE:' Zhurnal prikladnoy khimii, v. 38, no. 12, 1965, 2740-2744 ..-ITOPIC TAGS- emulsion polymerization, methacroleiri, catalytic.polymerization, high polymer, polymerp acrylic plastic P. IABSTRACT: Emulsion polymerization of methacrolein was studied in the presence of -1 ipotassium persulfate and.silver nitrafe*-w,ith a solution of polyacrolein bisulfite as, la apecific emulsifier. The object of the workwas to develop a process for making a Asoluble polymer with high molecular weight containing reactive aldebyde groups, The optimum ratio of the monomer to water Is 1:8 and the optimum polymerization tempera-: turo is 500 C. In all experiments the emulsifier content was constant (5 wt % based ion the monomer). The pmount of the initiator varied but the ratio of silver nitrate 4,1 UDCitli78.74 L -13082-& !ACC NR: AIP6002215 f at W at 70 - df L 6__B Fig. 2. The effect of solution pH on Z 4 6 polyacrolein characteristic vlscosity~q and polymer yield for 6 hr polymeriza- Fig. 1. Polyacrolein characteristic vis- tion and K2S208:AgNO3 ratio of 0.6:0.0 q cosity n asa function of polymerization , mole duration. A characteristic viscosity q; -in B~- is polymerizdtion duration hours; A - n; B percent conversion; V.- ini- the ratio of K2S208 to AgNOS:in mole'%; tial solution pH; 1 polyacrolein I - 0.6:0,06; 2 - 0o6:0.06 (in presenoe of yield in percent; 2 polymer charac-. a buffer)q 3 and 4 1.3:0.13; 5 2*6t teristic viscosity q. 3 _ 0;O0006geo0o off 09 o a "1 9 0 I " a a I I _11,_ 11 1 - I I IV It L Al A f. A A- A Al-I A .4 Pi-0.91st go. F pelf 'EVOWICS -6f. 0 goes* 000000000001W 0 I A- 0 A 0 orliol.__ fol ,-The gynthells of viliefa 9( thr- 1,3-dicialkiro- &ad -df- . Andrveva still I.- N. . tromakyoldne of I. N " so Ir t, I , SNUmlim Vormir.-h. GosudaW, chrinov. val MCA . Wly so t Org, Kkim. 1193fl. Pi. 1. 73 %1: KAim. dividestshyddo wims.A.talard Nora AeCl six) the ilk loto- -mi s t w P0% h d ld f l t. a o e ctsk e pro uc t apt hydrin, The Vir and that to( the purv product dirpmc 00% bit 1q4. 1mr, $ 1 4571. Utz esttr (as well as all o1her it 4" mV 1 . . . , raQy Vol. In MeM 1 in tmnlctw and water eActs) I- Instol ; , still U1011. AcONt. CIICIa samal other lotti. sialyttits. The drio% wiv% o1stainell with sk oomb ven4 d1hi t l t t avor i ield t e ti s -v ) A took 11t$' of crude or "N" tal tuiv Illodlit'j of Sl y 11 1 d , . ,v I .879, and ms%r 1.5141. 1rhe v iltnuoicrtate of t1yettol 4 . dichl urroloydrin was obtained front the dirldofohydTin still cielItCOM 'nif Yield W t Ito rate potoduct WAA 71 %, b. W-41" ago I 'At poll 1 4AM The chlottucctiall, A k`ha was :411jahard Its a milliho 1. l evrol JIQM,ji~ a r ~d The yiehl *Av:bL,O%. Ili, " 1113", ilk, 2 146. 10%,1 It was not poomalble to symbesize the bv;~tlat. .4 gly'l-tol dichlam- or dibrorwhydrin. W R~ Mean AIMLUWGKI~ 11MItOf CWIWKAT" s-ft. 11*-.-A,,%;- /-1 islesi) "it "v Got 414131CON-11 boliall OK Olkv ask AM L U 0 AV 10 1311, 0 1 0 0 0 0 0 4 -00 .00 000 '00 see 400 see its 0 coo ANTJUw-TwVAY I. V* ANDREYEVA, I. V.--IrIU Synthesis and Polymerization of ViVl Deriva- tives of the Furane and Thiophene Series." Acad Sci USSR. Inst of &-gh-Moleculw.- Compounds. Leningrad,, 1955. (Dissertation for the Degree of Candiate in Chemical Science). 60 Knizhnaya letopial No 2, 1956. 15-57-10-14441 Translation from: Referativnyy zhurnal, Geologlya, 1957, Nr 10, p 177 (USSR) AUTHORS: Andreyev, P. F., Andreyeva, I. V TITLE: The Internal Structure ot Paraffin Oils (K voprosu o vnutrennem stroyenii parafinistykh neftey) PERIODICAL: Tr. Vses. neft. n.-i. geologorazved. in-ta, 1956, Nr 95, pp 355-383. ABSTRACT: Paraffin oil is believed to be a system consisting of a dispersing medium (liquid hydrocarbons) and a dis- persed phase (heavy tarry substances and solid hydro- carbons). The materials of the dispersed phase ere capable of mutual adsorption and formation of complex Card 1/1 aggregates. G. A. Gladysaeva Ueu WN". VIM v I A,,J--...nJ '%I V raie-n- ht ilid- indimitcri ttmus. the aciivation enerrv fw iwt~ojdf- catak. Id Im Itill:, -- .. -- !~~! 1,-11. Tt-'~~t tt~41 YUAYk --I-X---KOTON, X.M. Synthesis of vinvl derivatives of the furan series. Zhur. ob, khIIC 27 n.o.3-.671-677.mr '57. (NLRL 10:61 1. Institut vyookomolei:~IiarnAh soyedineniy Akad'smii nauk SSSR. (Puran) (Vinyl compounds) DI 4Z4j/'4E-Dc (j 4 E 3J ~11) and .ix~ut A) II.Api-I 74 71j! 1.66m. I ills J;)rr-iexaL)IV ill fit(. cn de statc It) improve thr i,-I I 'x Lj~ Cal gave tile o,rtr,.I.)Fjtil g c".11kall"I to'l l'.1.,l,-d VIA-lig 1" file A AUTHORS: Andreyeva, I. V., Koton, M. M. 706-32-5-4/47 TITLE: The Influence of the Structure of Monomers on the Polymeriza- bility in the Series of Vinyl Derivatives of Furan (Vliyaniye stroyeniya monomer~,v na sposobnost' k polimerizatsii v ryadu vin.illnykh proizvod-nykh furana) PERIODICAL: Zhurnal fizicheskoy khimii, 1958, Vol. 32, Nr 5, PP. 991-994 ('USSR) ABSTRADT: The influence of the increase in number of condensed benzene k ~ngs in the initial monomers on the polymerizability and on some other properties was investigated; for this purpose "- -vinylfuran, 2-vinylbenzofuran and 2--vinyldibenzofuran were synthetized. In the determination of the polymerization kine- tics in the block close to the benzoylperoxide a modified - mercury dilatometer according to L.I. Yefimov was used, while in using ionic catalysts a catalyst according to Schlenk was taken. The characteristic viscosity and heat resistance of the investigated Dolymers were determined by the IFL instrument-and are given on Table 29 together with the obtained values of activa-,'Lon energies. From the experimental results obtained C&rd 1/2 can be seen that the velocity of polymerization in the series The Influence of the Structure of Monomers on the 76-32-5-4/47 Polymerizability in the Series of Vinyl Derivatives of Puran of 2--vinyldibenzofuran- 2-vinylbenzofuran- 2--vinylfuran in- creases which is in agreement with the obtained values for the aotivation energies; it was also observed in the case of using an ionic oatalyat. In the same order also an increase of the molecular weight and of the heat resistance of the corres- ponding polymers was observed, a..-. well as an improvement of the dielectric properties, which corresponds to the data of refer- ences and to the data obtained. There are 6 figures, 2 tables, and 5 references, 3 of which are Soviet. ASSOCIATION: Akademiya nauk SSSR)Institut vysokomolelculyarnykh soyedineniy (Institute of High-Molecular Compounds )AS USSR) SUBMITTED: June 19, 1956 .1, Fi-ran derivatives--Polynterizatior, 2. Vinyl compounds (Pol,Yme--ized) 3. Viul compound s- --Chemical reactioi)s Card 2/2 AUTHORS: Anareyeva, I. V., Kotoni M. M. SOV/76-32-8-19/37 TITLE: The Effect of.,the Monomer Structure on the Polymerizability of Vinyl Derivatives of Thiophene (Vliyaniye stroypniya monomeroy na SPOBobnost' k polimeriZatBii Yinil'Inykh proiz~vodnykh tiofena) PERIODICAL: Zhurnal fizicheskoy khimii, 1958, Vol. 32, Nr 8, pp. 1847-1850 (USSR) ABSTRACT: According to.data in publications the derivatives mentioned above are cap~tble of forming polymers having,dieleotrio pro- perties simikar to those.of polystyrene and having a higher softening temperature. An investigation of these compounds is also interesting as the influence exerted by,the type of dif- ferent substituted heterocycles in the ethylene'molecule may be inybotigdted with re-elect to the polymerizability and the properties of the compounds obtained. In 'he present paper the number of oondensed benzene rings in the initial monomer was inoreased, and therefore 2-vinyl thiophene and 2-Tinyl dibenzo thiophens were synthesized. The polymerizability was investi- gated according to the ailatometria method, viz., in the first solution with 0,5 mole% of benzoyl peroxide (in block and Card 1/2 solution)l and in the second in solution at B01 90 and 1000. BOV/76-32-8-19/37 The Effect of the Monomer Structure on the Polymerizability,of Vinyl Derivatives of Thiophene The operation technique has already been described. It was found that analogous to the furfurans series the introduction of condensed aromatic rings into the ethylene molecule in- creases the rate of polymerization. Besides the heat resistance increased to more than the double and the dielectrio properties also improved oft the occasion of the transition from 2-vinyl thiophene to 2-vinyl dibenzo thiophens. A comparison of the polymers obtained With than of the furane series shows' that the latter exhitit wore& prop'ertiesi There are 5 figures and 10 references, 3 of which are Soviet. ASSOCIATION: Akademiya nauk.WSR~Institut vysokomolekulyarnvkh soyedineniy (AS USSR,Inbtitute of High-Molecular..Compounds) SUBMITTED: March 21, 1957 Card 2/2 50) ATITHORS: Andreyeva, I. V., Koton, M. M. SOV/62-59-3-28/37 TITLE: On the Polymerization of a-Methyl, Styrene in Solid (Frozen) State (0 polimerizatsii a-metilstirola v tverdom (zamorozhennom) sostoyanii) PERIODICAL: Izvestiya Akademii nauk SSSR. Otdoleniyo khimioheskikh nauk, 1959, Hr 3, pp 552-553 (USSR) ABSTRACT: This is a brief communication on the polymerization of styrene in the block with gaseous 73 in solid state at -800 (freez- ing point of styrene -230) in an atmosphere as dry and free from oxygen as possible. Under the same conditions a-methyl styrene was polymerized in a yield of 85 %. The polymer is soluble in organic solvents (benzene, toluene, chloroform, etc) and Is precipitated from methyl or ethyl alcohol. The data on the polymerization kinetics of' -i-methyl styrene are given on a figure. As may be seen from it, the pressure of gaseous BF 3 in a block (without cracks) exercises only an unimportant influence on the polymerization of styrene. From the data mentioned in the table it may be seen the the yield of poly- mera, their molecular weight and the melting temperatures Card 1/2 increase with the decrease of the polymerization temperature. q On.the Polymerization of a-Methyl Styrene in Solid SOV/62-59-3-28/37 (Frozen) State There are 1 figure, 1 table, and 1 reference. ASSOCIATION: Institut vysokomolekulyarnykh soyedineniy Akademii nauk SSSR (Institute of High-molecular Compounds of the Academy of Sciences, USSR) SUBMITTED: July 18, 1958 Card 2/2 !Z_7 28650 S/020/61/139/006/017/022 B103/B101 AUTHORSi Koton, M. M., Corresponding Member AS USSR, Andreyeva, 99 Andreyev, P. P., and Rogozinaj E. M. TITLEt Comnlexea of polyacrolein with heavy-metal salts -3-,. -.. . PERIODICALt Akademiya nauk SSSR. Doklady, v. 139, no. 6, 1961, 1372-1374 TEXTt It is noted that samples of polyacrolein powder obtained under different conditions differ in their ability to form coordination complexes with heavy-metal salts. The strongest ability to cause such reactions has ura-,kyl nitrate. In the pH range investigated salts of Fb, Co, Mn, Cu, N-4, and Fe are not able to form stable complexes with polyacrolein. Conoerning the extraotion of heavy-metal salts with organic compounds, the authors refer to papers by V. M. Vdov *enko (Xhimiya urana i transuranovykh elementov (Chemistry of uranium and transuranic elements) Izd. AN SSSR, 1960) and V. 1. Kuznetsov (Usp. khim., 31, v. 6, 654 (1954)). The maximum quan-.i+.y of uranlium (2305-10-6g/g) was extracted from aqueous solutions by means of polyacrolein samples obtained by polymerization of acro.lein in Card 1/3 28650 5/020/61/139/006/017/022 Complexes of polyacrolein with heavy-... B103/B101 aqueous solutions under the action of the redox system K 2S208+ AgNO3 which is somewhat more effective than. the system K 2s 208+ Mohr's salt. Disacryl and polyacrolein obtained under the action of K 2S208 + Na2 5203are less effective. The poorest extracting agents are samples of polymers obtained at low temperatures in the presence of boron trifluoriae or by means of lithium butyl. The authors established a relationship between the content of alda~qde groups which are able to form oximes and the ability to extract uranium from aqueous solutions. Uraniur can be extracted in the range of pH3 - PH4. Outside this range the percentage of extracted uranium drops q,;ickly. The distribution coefficients for different samples of polya,.rola~_n differ by a factor of ton (from 0-005025 to 0.04803). Uranium absorbed by polyacrolein can be quantitatively dissolved by dilute ECI. There are 2 figures, 2 tables, 4 Soviet ard 6 non-Soviet references. The reference to English-language publication3 reads as follows: J. S. A~iderson, Nature, jjA, No. 165 (1950)- Cari 2/3 28650 S/020/61/139/006/017/022 Complex9a of polyacroloin with heavy-... B103/B101 ASSOCIATIONs Institut vysokomolskulyarnykli soyedineniy Akademii nauk ' SSSR (Institute of High-moleoular Compounds, Aoademy of 4 Soienoes USSR) SUBMITTM April 81 1961 Card 3/3 ANDREYEV, P.F.; MDREYB.TAj,I,V.j ROWZINAt E.M. Reaction of uranyl salts with the components of plant tissue and some of its derivat'vea. GookhImlia no.4013-317 '62. (MIRA 160) ..(&an.vl salts) (Plant cells and tissues) '1, #_- 36292 sl19ol621004100410081019 B119/B136 AUTHORS: Andreeva, 1. V., Koton, 11. M., Kovalevaq K. A. TITLE: Polymerization of acrolein and its derivatives. I. Low- temperature polymerization of acrolein and a-methyl acrolein PE11IODICAL: Vysokomolokulyarnyye soyodineniyap V- 4t no, 4, 1962, 526-532 TEXT: Acrolein (1) and a-methyl acrolein 0 (2) were polymerized in the preuence of gasco*as BF3 between 0 and -60 C in block and in solution (solvent: CH 2C1 2) . The experiments were made in sealed ampoules, partly with exclusion of 02 and H 20, partly in the presence of very small amounts of H2O-Results4 Polymers obtained in block polymerization with 10-15rlfo conversion are completely soluble in organic solvents. With a higber deGree of conversion, the reaction product becomes insoluble in organic solvents but soluble in sulfurous acid. The reaction with 15-2MA conversion without H20 takes 15-30 hr at -20 0C, with H20, 3-8 hr. Card 1/3 s/igo/62/004/004/008/019 Polymerization of acrolein and its B119/B138 The molecular weight of thd polymer produced in the presence of H20 is lower than in the one produced without water. Maximum conversion was attained at -20 to -40 OC with 1.5 mole% BF (with 1) and 2.5 - 3 mole% 3 (with 2). The block polymers give no aldehyde reaction, they are cyclized: CH CH CH 2 2\ 2\ 7H VH CH CH Polymerization of acrolein in solution CH 0 /CH 0 ICE 0 /,C 0 givon a soluble product*%vith a melting point of 150-170 C and JI'l (,.06 - 0-07 in benzene at -600c and 301o conversion, but an insoluble and nonmelting product at -200C and 30% conversion. The polymer obtained from dilute colutions is not cyclized. At -200C the rate of polymerization decreases in the order acrolein a-methtyl acrolein - a-ethyl acrolein. There are 4-figures and 1-table. Card 2/3 E 075/E436 AUTHORSt Andreyon., _I-V Andreyev P.F#, Rogozina, E.M. TITLE: Investigation of the process -.d products of interaction of high molecular weight compounds with inorganic salts. I. The formation of polyacroleir.~. complexes with urpnylnitrate PERIODICAL ho.6, 1962,,66o-667 F Radiokhimiya, v TEXT: The complex formiag ability of,various polyacroleins was examined for the'first time. This work forms a start of a long-tcem investigation of complex formation between metals and' the derivatives of polyacrolein and other-polymers with carbonyl groups. The polyacroleins investigated were obtained by 1) polymerization of acrolein in water in the presence of oxidation-reductI.on initiators; 2) polymerization of pure, dry acrolein without initiators; 3) low temperature (-200C) polymerization in the presence of traces of H20 or BT 4) polymerization In benzene solution * Na; 5) bloc polymerization in the presence of lithium butyl at 200C. The complexes with U02(NO3)2 were formed in-aqueous solutional their..~' Card 1/ 2 ANDREY(EVA, I.V., KOTON, M.M.; KOVALEVA,, K.A. Polymerization of styrene derivatives in the solid (froxeA) Oute. Izve AN SSSR.Otd,khimenauk no.lq:1890-1891 0 162. (NIRA 15:10) 11 Institut aokomolekulyarnykh soyedineniy AN SSSR. (Styrenle (Polymerization) ANDRSX3VA,, I.V.,- AMRMV) P.F.; -RWMINA) S.M. Proaasswand.interaotton produets of macromolecular compo=ds with,inorgazLic Part 2: Formation of corplexes of poly(purmethyl)acr ein w-Ith uranyl nitrate. Radiokbimiia 5 no.1:103-106 163. (MIRA 16:2) (Acroloin) (Uranyk nitrate) (Maeramoleoular compTaids) S/020/62/144/005/013/017 B I 24/jB 138 op to AUTHORS: Koton, IL M.; Correoponding Member, AS USSHf Androyeva, 1. V-j and Getmanchuk~ Yu. P. 71TLE: Emulsion polymerization of a-methyl acrolein in the presence of various redox systems PERIODI.CAL: Akademiya -iauk SSSR. Doklady, v. 144, no. 5, 1962, 1091-1093 TEXT: a-methyl acrolein was polymerized in various redox systems in the presence of a new type of emulsifier, aqueous polyacrolein sulfite. This yields a stable emulsion, and polymerization takes place in the micelles of 'IV the emulsifier. Polymerization is carried out in ten times the amount of V11, water with audition of twice the amount of a 2 % aque-ous emulsifier, all related to the monomer usuld. The most suitable redox system for thi's scope is potassium persulfate and silver nitrate which gives high polymer yield6 of maximum molecular weight. All a-me,thyl-aoroloin polymers obtained contain 65-70 ~ aldehydic groups, while for polyacrolein preppxed in the same redox ssstems this figure is 20-70 %6 This ib due to the mothyl group in the side chai.n ckf the a-methyl aorolein molecule, which pievents the Card 1/2 KOTON"M.M.j ANDaEYLVA,,I.V.; ANDREM, P.Y.; DANILOV, L.G.; RDGOZINA, E.M. Reaction4, 9f an aqueous solution of polyacrolein with inorganic salts. Dnlkl,.AN SSSR 146 no.3:60f-61q, S 162. (KIRA 15:10) I* Institut vyaokomolekulyaruykh soyedinsaiy AN SSSR,,-2,, Chlen- korrespondent AN SWIM (for Koton). (Acrolein) (salts) (Macromolecular compounds) KOTON, M.M.;.~VDRE _-I,.V.; GEIMANCHUK, Yu.P. Polvmerization of meta-acrolein with anion catalysta. Dokl. AN SSSR 155 no. 4:836-838 Ap 164. (MIRA 1-1:5) 1. Institut vysokomolekulyarnykh soyedineniy AN MO. 2. Chlen- korroupondent AN sssR (ror Koton). ANDREYEVA 1.V,; AND."MIMN, P.F.j DANILOV, L.T., ROGOZINA, E.M. Processes and proiucts of the in' raction of high-molecular weight compounds with inorganic alts, Part 31 Reaction of aqueous solutions of polyacrolei .. ladioklilmlin 6 no. Is 86-93 164. (WRA 17%6) ACCESSION NR: AP4020057 SJOIU616410061001/0086/00h AUTHOR: Andreyeva, 1. V.; Andreyev, P. F.'; Danilov, L. T.; Rogoz4na, E. M TITLE: Processes and products of reaction ot high molecular compounds with inorganic salts SOURCE: RadiokhlmiyF-. v. 6. no. 1, 1964, 86-93 TOPIC TAGS: polyacrolein inorganic salt reaction, polyacrolein reaction, polyvinylalcohol, coagulation, gel formation, metalprecipitation, variable val- ence metal reduction, polyaldehyde, hydrated aldehyde group, t:horium polyacro- lein complex ABSTRACT: In continuation of earlier work L polyacrolein and its ability to ex- tract metals from aqueous solutions, a number oi reactions were run or attempt- ed between 3% polyacrolein and 3% mineral salt solutions. Aqueous solutions of polyacrolein have a series of characteristic properties explained by tne presence of an external hydrate shell and hydrated aldeny'de groups for the polymeric mol- eculq: ard 1 ACCESSION NR: AP4020057 acid medium. The complexes formed have constant compositions, differing depending on pH of the media. In acid solution one thorium atom is complexed with 24 or 28 elementary ligand links; at pH 4. 73 and 8. 32, with 8 and 9 linicages regardless of the ratio of the reactants. Reaction with potassium bicnromate and ammoniacal solution of hydrated copper oxide gives, as do polyvinylalcohol solutions, galn which are insoluble in water. The structure of the polyacrolein- hydrated copper oxide complex may be represented by geiation of polyvinylalco- hol. Preliminary data obtained indicates that elements with variable valence can be reduced with aqueous polyacrolein solutions under determined conditions. It is therefore assumed that the polyacrolein molecule can react as a polyalde- hyde. This capacity of polyacrolein for many chemical and physical- chemical conversions makes it a theoretically and practically interesting material. Orig. art. has: 4 tables, 7 formulas, wd 1 figure. ASSOCIATION: None SUBbUTTED: Mept12 DATE ACQ: 31MarG4 ENCL: 00 SUE CODE: VTj GG NO REF SOV: 003 OTHER: 005 Cord3/3 L 16o88_6c;_,. E;W.T(m)/EPF(0~jV_zP -CCE 8 S I ON -Of-7 AM 91 3-.- ":V6020/64/ 159 /003/0602, egIM51i XI~TrOlgpon --uw-_ 77~ 'i k-il V _Yav G TITLE t f h ketone polynerizatt o- giroxy2henyl vinyl SOURCE: A9 SSSR. Dokl,adyh, v, 159, no. 3, 1964, 602-604 ..TOPIC TAGSt chel-ate polymer, o-hydroky.phenyl vinyl ketone, polymer, 1 metal chelats copolymex,, Methyl methacrylats, divinylbenttne: B - S T RA ZT i ; T h 7 i n--d -t _16 at4on d t vme -tu'dfed-_rh_7_i__1e_ -o-r t ~_qob_tain ---- po-:Ly-~ tViny'l- etone~ rige-r-5---c-on ny 9 t'--" i it at on or cop -0 lyme ri 2-4 t-i ,on T 7 _~f ___ -, - -1 - . t -'a ze specidlly-16r th --- + he o_-hydrbxyph0_tiy1--viq1-' i 1 oi'n e'- 9 Q e 'study' was'polymerized in-,a* nitrogen atocaphere by su'veral methodst i . - 11 R - . .. I- 6 _bu~lk, ind i il :9 : -'-- '. on -do Goluti Ln f a I'ators if PbLymer a tion. Cz V -1 ------- 75'- 8.M 'col-orle6s-, (af ter reprecipitaki )'..powde -amp a ra ure~was T a like polymer Is L 16088-65 ACCESSION NRt A?4049923 acetonei, pyridiue,,-or--diuethylformemides and in dilute alkalis: it insoluble In methanol, carbon tetrachloride, or ethyl ether. The imolecular weight of 125,000 vas-determined by the light-dispersion !method. The intrinsic viscosity of polymers depends on the method of lobtaining them. The lovest-Wes were obtained for the product 1polymerized In solution; the bIgheatp Ir suspension. The kinetics of; ithe polymerization were studied, and the curves and the constants ~wara obtained. The IR -spectra- confirm that polymerization takes placi 7 only along the double bonds-* -The a2ime derivatives confirm the pre- ~sence of the theoretical number of carbonyl groups in the polymars .obtained. Products of q2yolymsrizationqof o-hydroxyphenyl vinyl - - :ketone with methyl methaery.ate (br dMi4ylbenxene were also obtelned;t _properties~. The presence-of the latter Product hWs-Ion_s-z0h4#ge ps -in the polymer# studiod makes it possible to us chelate grint these p____, piers' or--copolymers-1 or __o4t*.InInj_.;polymeric, -complexes --with -talss],~ oly :e i e4R.17 an 9 ASSOCI a 'k AfIONJ~ i-.':IUiBtitUt~vy,*46kasolak'Ul~1 rny hsoyeeineniy'AkadevfW~nauk (In' titut --of -Mactolviidlelii~ulalr--Co c an C a vapounds Academy-of 6 1 -SOS ------- - - Card 2/3~ .U'kVlN, V.K.; AYMYLVA, I.V. I ------ Inactivation of the phage genome A by acridine dyes following infection with Fscherichia coli K12S. l4ikrobiologiia 33 no-5: 819-823 S-0 164. (lqiRA 18:3) 1. Institut biofiziki AN SSSR. ANDREYEVA, I.V.j RGGOZINA, E.M.; ANDRMV, P.P. 'Processes and products of the rpection U high-mole-cular coiffpounds idth Ifigrg'anib aalts.-Part 5t rhysicochemical studies of the reaction'bf pol~acrolein with inorganic salts. RndiokhiTniis 7 no 01:83-90 163. (MIRA 18:6) RAVI 11, V.K. -. J~ i% P! &: Yl-, VA , I.V. Effect of ultraviolet irradiation on the temperate phage-tecteritm complex In various stages after its formation. 14.1krobiologlia 34 iic-~.IMC-113 Ja-F 165. (MIRA 18:7) 1. Inotitut biologicheskoy fiziki AN SSSR i Institut mikrobiologii i epidemiologii Imeni N.F. Gamalei AMN SSSF. GFRSHANOVIC-3,11, V.N.; BURD, G.I.; _MOTLEYEVA, I.V,; .njD,,V, V.A. Effect of phagm T2 "ghosta* on the synthesis of inducible beta- galactoBidase in Eacherichin coli B calla. Bickhimiia 30 no.2: 395-406 Mr-Ap 165. (MRA 18:7) 1. Institut, epidemialogii i mikroblologii imed Gamalai AMN SSSR, Moskva. ANDREYFVA,, I.V.; XESHV*.%'AN, G.O.; ANDRRYEV, P.F.; DANILOV, L.T. Processes hi.1 products of the reaction of macromolecular com- pounds with inorganic salts. Part 4t Reaction-of aqueous solu- tions of polyacrolain with tannin and gelatin in salt solutions. Radiokhimiia 6 no.4t491-493 164. (MIRA 18:4) ACC NRAP6034385 SOURCE -COI)9;.--W/0-4W/66-/000-/005/0~r)T3/057 AUTHOR: Ravin, V. ORO: Institute or B4ophysicap AN SSSR (Institute bioloricheakoy fiziki AN MR); Institute of EpidemioLogy and microbiology im. N. F. Gamaleir AmN,SSSR, Moscow (Institut epidemiologii i mikrobiologii AMN SSSR) TITLE: A mutant or x bacteriophage resiztant to acridine-orange SOURCE: Voprosy virusologii, no.. 5. 19660 575-578 TOPIC TAGS: virology, cytology, immunology, ~bacteriop~age, DIV) ABSTRACT: A mutant of A bacteriophage resistant to acridine orange both vithiq and outside the cell was obtained from cultures of 96 coZi K 12k. The mutant was sorologically identical to wild-type phage, No differences were noted between strains in lysogenic capacitys sensitivity to ultraviolet UDC:576.856.9-695-57-097.22:615-778.292 AUTHORS: Yefremov, G.V., Andreycva, I.Yu. 54-10-2-12/16 TITIE: The Co-Precipitaticn of Thallium and Cadmium Sulfide fSoosazhdeniye talliya s sul'fidom kadmiya) PMT-ODICAL: Vestnik Leningradskogo Universiteta,Seriya fiziki i khimii , 1958, Vol.1 0 , Nr 2 , PP- 117-121 (USSR) ABSTRACT: I.P. Alimarin (Ref 1) and other authors showed that cadmium sul- fide is a good collector for microgram quantities of thallium. In view of the quantities of thalliwn that are usually lost in pro- duotion and because of the difference in the conditions of co- precipitation, the authors studied the oo-precipitation of thal- lium with cadmium sulfide. Final determination vas carried out ac- cording to the calorimetric method by the application of methyl violet after oxidation of the thallium by bromine,water. Under prevailing conditions the 10nslOmr? and dcl~ are formed, which, according to data' supplied by II.T.Voskrese kaya (Ref 4) form com- 4 pounds with vat dyes mid thereby render the determination of thal- lium difficult. It was found by an investigation of this develop- ment that if UP to 75 milligram of cadmium are present, the in- Card 1/2 fluenoe exercised b-r the ion [OdBr,)" is so small that it is hardly The Co-Precipitation of TIkillium and Cadiaium Sulfide 54-10-2-12116 manifested at all in results obtained, nor vas thallium determina- tion i-nfluqnced in any Ymy by the presence of the ion [CdCl 7 " un- der the same conditions. Average values of the precipitatD per- centage of thallium for different correlations of thallium., cadmi- um, and pH solution are given (table 1). It may be seen from this table that the highest co-precipitation percentage is found at PH 5-5,6. Both an increase and a reduction of pH, conditions other- wise remining the same, leads to a reduction of the percentage. Precipitation of sulfide vas, in the case of all previous experi- ments, carried out at a temperature of 70-800. At lower tempera- tures precipitation is finely dispersed, and therefore co-precipi- tation of thallium increases. At low precipitation temperatures (200) the coagulation of the precipitation is made difficult. For a long time it remains in the form of sol (table 3)- In the case of repeated precipitation of cadmium. sulfide thallium can practi- cally be fully eliminated. The values obtained show that the co- precipitation of thallium Yrith cadmium sulfide takes place mainly at the expense of surface adsorption. There are 7 tables, and 4 referenoes,&U of which are Soviet. SUBMITTED: December 25, 1957 AVAIIABLE: Library of Congress Card 2/2 1. Thallium-Precipitation 2. Cadmium sulfide-Precipitation 3. Thallium-Datermination 4. Cadmium sulfide-Determination 5. Colorimetry-Applications YM2WOTV Copmol itation of thallium with cadmium'sulfide [with suzmaz7 in 3tagimb Vast. IGU 13 no,lOtll7-121 158, (MIR& 11W (Thallium) (Cadmium sulfide)- S/032/601/026/012/012/036 B020/BO56 AUTHORS: Fraiki`nj Z. G. and Andr .TITM The Spectroscopic Analysis of Impurities in High-purity Sulfur PERIODICAL: Zavodskaya laboratoriya# 1960, Vol. 26, xo,. 12, pp. 1370-1371 TEXT: Two methods of determining the purity of high-purity sulfur by means of spectrum analysis were worked out, namely the direct spectroscopic de- termination and the determination with previous enrichment of the sampke. Work in this field was carried out by A. N. Bronshteyn and L. M. Ivantsov (Refv-1). In the oassi of the first me'thod, the standards were prepared in such- a- manner that the e,',,eme,nts Fe, Co, Cu', Ag to be determined were mixed, is sxklfid9i,Aog9ther with sulfur into a jasper- or agate mortar, and alu- .%4um was introduced as Al 20 30 The spectra were recorded by means of the ,speotrograph WCn-28 (ISP-28). Aa exciter, an a.c. aro with an amperage of 7*k was used. The sample was pressed into the channel of the lower carbon electrode, whose diameter was 3 mm and whose depth was 4 mm. The upper Card 1/4