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SCIENTIFIC ABSTRACT VOLOKH, S.M. - VOLOKHONSKAYA, YE.S.

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CIA-RDP86-00513R001860710007-1
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December 31, 1967
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SCIENTIFIC ABSTRACT
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M M IMP'lir 111P a 1111; a III SIR vIF v TV 11 v a 2, a ; v 0 OR u Is to is 10 1 m IF a is IF 00 4 ['60 7114 ~11 .*.CRISIS 16~.Iw,fs , so IR -410 'go _ III Sit reeding the aulls with supeolicalmIJ vapots of the csode Kkos, to 47 J. 0V lot Mil"Int Inj Willi *111WIlit'41411 Thr U" 4 mlfi~fh%'Alfll VAIVIIII, it Whfn lM1%iAkI1% MIIV Piripplost llo-ch =00 coo MIS .1q.. 1111141 tufaw" .6. aow, J.t Is. A-4 v IA 111 AT 10 f Is --Ir 4A A A 0 1** I's 0 glis 0 0 f 0 sm, 00090 VOLOKH, S. M. 42376; VOLOKH, S. M. 0,raskhode rast voritelya pri ochiatke masel szerbqydzhk. Neft. khoz-vo 1948, lio. 1'w, s. 14-16 SOt Latopis' Zhurnal'nykh statey, Vol. 47, 1948 BLAaOVIDOV, I.F.; SPZXTOR. Sh.Sh.; UDALYY, A.M., vedushchly redakior; VOLOKH, S.M., professor, redaktor; ISHATLOV, R.G., dotsent, redaktor [Operation of oil refineries) Ikeploatateiia nefteparerabaty'vaiu- shchikh savodor. Pod red. S.H.Volokha i R.G.Immaileva. Baku. Goo. nauchno-tskhn.Azd-vo neftianot i gorno-tiplornot lit-ry, Azarbaidshanskoe otd-nie. 1951. 199 p. (Kicrofilml (MLRA ?:10) (Petroleum-Refining) Subject Card 1/1 Author Title USSR/Chemistry AID P - 1786 Pub. 78 - 24/26 t Volokh, B. : Bagaturov,, S. A. Kure teoric peregonki i rektifikateii (Text-book on the Theory of Distillation and ctification) Gostoptekhizdat, 1954. 478 pages Book Review) r Periodical : Neft. khoz., v.33, no.3, 94-96, Mr 1955 Abstract This text-book on the thermodynamic theory of distilla- tion and rectification (fractionation) is favorably -reviewed. The book is approved by the Ministry of Hiiher Education of the USSR as a text-book for students of Snatitutions of higher learning. Institution: Submitted None No date To professor; MROVO Y.M., redaktor: SHTITNGELO, re r zdatel'stva [Principles of a theory of extraction applied to purification of oils by solvents] Osnovy toorii ekstraktaii primenitallao k ochiatke masel rastvoriteliami. Baku, Aserbaidshanskoe gos. izd-ro neft.i nauchno-tekhn,lit-ry, 1957- 91 P- (MMA 10:9) (Patroloun-Refining) Vol, 0 k H S" Y" I SHIRDZHAIIDV, i;uf Tairovich. dote., )mnd.tb'zh:..nauk; YOLOKH, S.M., prof,, red.; GORCHAROT, I.A., red,izd-,ra (3kamplos of ca.l,culations of petroleum refine 7 processes and apparatus] Primery reschetoy' neftezavodskikh jroteessov, i apparatoy. Baku. Aserbeiftfionskoe gos. izd-vo neft, I no-.Lchn.-tekhn.lit-ry, 1957. 4.03 p (ML4A 11-4) '(Patroleuri--Refiaing) TOLOKH, S.M., prof. Regarding Othe theoretical plate." Azerb. neft. khot. 36 no-5:48 MY '57- (MIRA 10ill) (Diffusion) An lyzing liquid hydror-arbon solutions In p -frnct*cn,3t"rg ga a apparatus. Izv. vya. ucheb. ray,; nnft' I e,=, no. 5:110 158. (.kj IRA 1). 8) (5ilrocarbons KRISHNA, P.V.;, VOLOO) S.M., prof., ruko-oditell raboty Dew-matization of ke-rosi-e fra,~Ucna of secondary derivati, .IX using furfur-al. 1z7. -vYs. '~;cheb- zav.; neft' 4. gaz 6 nci.2:55- r8 165. 1. Azerbaydzhanskly institut nefti i khimli Im. M. Azizib~kova. AIRK IEV.. V.P.; VOLOKH, S.M. Analytical calculation of multicomponent rectification. Izv. vys. ucheb. zav.; n~ftl i gaz 3 no.5;127-131 160. (MIRA 15:6) L Azerbaydzhanskiy institut netti-1, khimii imeni M. Azizbekova. (Diatillationp Fractional) VOIDMi. Samil Markovich.. p rof.; KUTYUMOV., P.S.,, red.; ALITMAlip [Principles of accurate laboratory control in gas fractioning plants]Osnovy pravillnogo laboratornogo kontrolia na gazo- fraktaionUndiushchikh ustanovkakh. Baku, Azorbaidz-ban koe goo. izd-vo noftinnoi i nauchno-tekhn. lit-ry, 1960. 21 p~ (MIU 15M (Gasos-Analysis) VOLOKHj,_S.M..,P,'Of- Utter to the edit-or pertaining to B. N. Hikhailovski-i's article "Calculation 9f rectification colm-no b-ased on tlzeroreetica2 plates and vnitv of transfer." Izv.vys.ucheb.zav.;khim. i kbim.tekh. 3 no.2;386 160, (MIRA 14:6) 1. Zaveduyushchi]r kafedroy neftezavodskUdi i kbimichoskIkh apparatov i oborudovaniya Azerbaydzhanskogo instituta nefti i khimii Imeni 14. Azizbekova. (Plate towere) (MkhaUovskiiv B.N.) -VOLOKH, T.7. Stability of alcoholio solutions of an AG salt - FE -caprolactam copolymer. Xhim.yolok. no.1:17-19 160. (MIU 1316) 1* Kiyevskly kombinat. (Nexamethylenimine) AUTHORj Volokho T. F. 8/183/60/000/01/005/031 B004/BO14 TITLEo Stability of Alcoholic Solutions of the Copolymer of AG Salt With I-Caprolactam I PERIODICALs Khimicheakiye volokna, 1960t Nr 1, PP 17-19 (USSR) TEXTs A copolymer is produced by the Kombinat of the author from r-caprolaotam and AG salt in the ratio 60s40. The alcoholic solution of this copolymer is used for varnishing imitation leather and other purposes. However, only hot solutions of this copolymer are stable. When they are cooled, they solidify rapidly. The author studied the stabilization of this copolymer by means of various additions and by modifying the ratio of its components. The stabili- zation of the solution was checked by a method devised by the Kiyevskiy regeneratorno-rezinovyy zavod (Kiyev Factory for Regenerated Rubber). which is based on the determination of the time passing until the solution b;c'omes dull. The polymer taken out of the production proved to be so inhomogeneous that experiments had to be performed with samples prepared in the laboratory. The results obtained are compiled In table 1. Copolymers with 50% of AG salt and 50% of E-oaprolaotam and with 40% of AG aalt and 60% of E-oaprolactam were the most stable. Their stability is increased by adding 2% of benzoic acid, 10% of Card 1/2 Stability of Alcoholic Solutions of the Copolymer 8/18~/60/000/01/005/031 1of AG Salt With E-Caprolactam B004/BO14 formaling or 10% of carbon tetrachloride, as well as by treating the solid copolymer with 40% formalin (Table.2). A sample of this copolymer was dried at 0 1 1250 and then dissolved in alcohol with different water content. Stability increased with rising water content of the alcohol (Table 3). There are 3 tables and I Soviet reference. ASSOCIATIONs Kiyevskiy kombinat (Kiyev Kombinat) VOIDKH,, V.. -------------- "How to solve a problemn,by D.Poia. Reviewed by V.Volakh. Znan. ta pratsia no.2:30 F 162. (MIRA 15:2) (,,Ogie) (PoidiD.) 71-7 94v5aq VOLOKH, V. Drops of meteorites. Znan. ta pratsia no.1:1&19 Ja 162. (MIRA 15:1) (Meteorites) ALEKSANDROV, N.N.; VOLDKH.,- V.G* Efficiency of FPP-15 filters. Trudy 6G0 no.13806-59 163. (MIRA l7t2) 1 `., - 3t , I ". VOLOKH,,,V.G..; WSHCHINA, M.Y.; IGRTATOV, V.D.; NECHAYEV, I.N.; POIMOVSKAYA, I.A.; TRIFONOVA, T.S.; TSYGANOVI, A.M.; RUSIN, N.P., otv.red.; KITAYTSZV, A.K.i red;; KMININ, L.A., red.; OLIMPOV, Y.G., red.; SKITZUIHv- I.S., red.; BXRLIY. I.A., red.; NECHAYRY, I.H., red.; SHCMMAKOVA, L.P., red.; MARTYNOV, S.I., red.; SIHONOV, Ya.P.. red.; IVANOV, A.P., red.; BESSONOV, N.P., red.; YASNOGORODSKAYA, H.K., red.; VLADIMIROV, O.G., tekhn.red. (Directions for hydrometeorological stations and posts] Nastavlenie gidrometeorologichookim stantailam i postam. Leningrad, Gidro- mateor.12d-vo. No.3, pt.l. (Obsorvations at meteorological stations] Meteorologichookie nabliudeniia na stantaiiakh. 1958. 223 P. (MIRA 12:12) 1. Missia (1923- U.S.S.R.) Glnvnoye uprnvlaniye gidrometeorologi- cheekoy sluzhby. 2. Sotrudniki Hotodichookogo otdola Glnvnoy t,'.'3o- fizichenkoy observatorii in. A.I.Voyeykova (for Volokh, (hishchina, Igrunov, Nachayev, Pokrovskayao Trifonova, TSyganova), 3. Glavnoye upravlaniya Gidrometeorologichaskoy aluzhbv SSSR (GUGHS)(for KitAytaev, KU21min, Olimpov, Skiteykin). 4. Glavnaya goofizichookaya observatoriva (GGO) (for Berlin, Nechayev, Ihisin, Sherbakova). 5. Mestnyye upravleniya Gidrometeorologicheakoy sluzhby (for Kortynov, Simonov. Ivanov, BOB- sonov). (Mateorolo&v-Observations) R-F-TEIVRly, S-I.; NOMAROVA, L.I.: Prinlyrialt uchnatiYe: SKIBA, I.B.; BELAIISKIY, M.A.; VOLOKH V.Ya. Propagation of fodder yeast on corncob hydrolyzates. Gidroliz. i prom. 18 no.3:20-22 165. (MIRA 18:5) 1. VNIlsintezbelok. VOLOKH inzh. W"" ~tl 'P a ". . Using ~sinforced concrete in constructing arebad roofs. [Suggested , by IA. IP.Volekh.). Rate. i izpbr. oredl. v etroi. no. 4:5-8 157. (KIRA 11:8) (Roofs, Concrete) VOLOKH, Ye M Intra-arterial blood injection in mortal blood loss in obstetric and gynecological practice. Akush. gin. no.6:72-73 Nov-Doe 1952. (CLKL 23:4) 1, Of the Gynecological Division (Head -- D. M. Volokh), Ternopol' Oblast Hospitalf, VOWKHj YU. A. VOLOKH, YU. A. "Echinococcal disease In northern Kirgizia.n Kirgiz State Medical Inst. Frunze., 1956. (Dissertati6n for the Degree of Doctor In Sciences) A Medical so.- Knizhnaya i*topisl, mo. 18, 1956 VOLOKH, Yu. A.: Doc M-3d Scl (diss) "Echinococcosis of man. Experience in treatment, active detection of patients, and the organization of tll') floit against this invasion in the Kirgiz SSR". Alm-Ata, 1953. 22 pp (Kazald-4 State med. Inst), 300 CoPles M, No 5, 1959, 154) =ARNO" 5-M M VOLOKH.v Yu,A, Terminology and claosification of echinocqc~cosis. Izv. AN Kir. SSR. Ser. biol. nauk ^4 nq,,6:49-52 160, - (MM 14:6) (HYDATIDS) VOLOKH, Ya.A _ New method for studying the diffusion of echinococcosis in ran. Izv. AN Kir. SSR. Ser. biol, nauk 2 no.6;101-203 160, (KUM 14: 6) (KIRGHIZISTAN--HYDATIDS) --,YPPPs YU.A. , 11 Surger7 in liver echinococcosis. Izv. AN Kir. SSR. Ser. biol. nauk 5 no.3s77-82 (MIRA 17:1) AMUNBAYU, I.K.; VOLOKHj Yu.A. organizing control of echinococcle in Kirghizia. Izv. Ali Kir. SSR,'Ser, biol. nauk 2 no.6127-21 160o (JaRA 14t6) (MIRGHIZISTAI(-HnATIDS) VOLOKH, Yu.A.; M4YSHEV, S.B. , Echinococabois in southern Kirghizia. Izv. AN Kir. SSR. Ser. biol. nauk--2 no.6sla-48 160. f (MI.U 14: 6) (MRGHIZISTAN-IIY~ATIDS) m 0 VOLOKH, YURIY ALEKSANDROVICH M/5 644.192 EKHINOKOKKOVAYA BOIEZNI U LYUDDZY fFCffII40=COSIS IN HUYAc7 FRUVZ-I?, V9 IM40 AKAD5al NAUK KIRGIZSKOY SSR, 1957. 252 P. ILLUS., DIAGRS., TABLES. "LITERATURA"t P. 233-257. MANOR a RAN se-I la M B W R BELYAYEV, B.Ye., inzh.; BULAKH, V.F., lnzh.; VOIDKFp Yu.G., lnzh.; EVFNTOV, I.M., inzh. Unit for preparing road emulsions, Stroi. I dor. mash. 10 no.9sll-13 S 165. (MIRA 16:10) Vol HIN (Candidate of Veterinary Sciences) I~Jectlonofmmmificated fetu's fro'l cow wiX the aid of stilberstrol. So: Veterinariyal 22; (2-3); February/Mlarch 1-)45; Uncl. TABCON .- VOLOKM9 I.A. (pelo Dzvinkovoys Zakarpatskoy oblasti) Premerva.tion of vacoineo and sera in a vell shaft in a rural area. Felld. i akush. 25 no.6s46 je 16o. (min .13: 9) (DRUGS-PRERMATION) P.i.,KACIIEVSKAYA, OoP., VOLOKIIINA, FIMIRMYSEVA, ac-ld lactam with Z-1aprolactam ali(I I-Arvirithol tic tam. Vyaokcm. oned. 7 no.6; 1092-1097 Je 165. (101A M9) 1. Vse3cjyuzllyy nauclino-Issladrivatellskly institut l5k-asstvennogo volokrA. ARMAWO X#K,,q prof.; 'MKH Tuo-A# Itudy of thenrum prot~lix by the metbod of paptr aleartrophorsoin in patiento with eMemic goiter and schinooocoomis. Xhirurgiia 37 noi,5t79-81 my f61. (KIRA 105) Is Xx laboratorii andemicbeekikh zabolovemiy (sav6 - prof. I.Ke AkhunbaM) Tmatituti karevoy meditairq Akademii, nauk Kirgis- likoy $SR. (BU)OD PROTMS) (HYDATIDO) (GOIT3R) (PAPER MMTOPH.OFMIS) UK- ~5- i ' ~171 ~-It k ~V-x VOWKH, Yuriy Alekeandrovich:AKHURBAYNV, I.K.,akademik, ~ed.;YMMOV,V.A.,tekhn. red. ~Lgchinococcus In humans] NMinokokkovala bolezn' u lludei. Frunze, Akad.neuk Kirgizokoi SSR, 1957. 259 P. '~(MIRA 11:1) 1. Akadml$a nauk Kirgizekoy SSR.(for Akhunbayev). (HYDATIDS) VOLOKHIN A E. (Asst. Professor, Voronezh Zooveterinary Inst) "On the Question of the Naturej Classification and Control Memaurea in the Liquidation of Sterility in Agricultural Animals on Kolkhozes and Sovkhozesm Report given at 13th Inter-VUZ (Higher Educationa Inats.) Scientific-Industrial Conference, held February 1956 at Kiev Vet Inst. voL M IN, A. E. (Cana. of Vet. Sci.) "Middle uterine arteries and diagnosis of the periods of calving in covs." SO: Vet. 25 (12), 1948, P. 34 VOLOKHTN, A.V. Volokhin, A.V. -- "Several Questions on the Density of f ( )." Cand Phys-VAth Sci, Gor'kiy State U, Gorlkly 1953. (Referativnyy Zhurnal-FAteratika, Jan 54) SO- SUM 1680 22 July 1954 VOLOXHIN, I*P* (Borisoglebsk) Need for more extensive specifications in the present price lists. Shvein.prom. w.ls34 Ja-F 162.' (MMA 15 14) (Clothing industry-Specifioations) MP -7 8 3/6 5/OOO/OC2/0D75/DC"6 AMi~;;.. Voloiuhina, A. 2l.; Ycretskz-fa, TITLE: Fifteenth ronference on High -YL-lecular ~Ompouxids SOUPCE, nimicheskiyo v,)lokna, 11-0. 2, 1965, 75-76 TUN, TArZ: polp-jer, chpirricnI r-onfpr-PTICO, macromolnciilar cheridstry, heat property ABSTRA"', The 15th Conf,~7encc c,.~! TlikVl-%T()lecuL)r Compcund[i, huld 25--~8 jan- I'lat was divided into tvvo secticms- the firE,,. r-ection d(-.-,Ilt with the Y rynthesis 'of n(-w polymerb and the second, with polymut- modification. ',.I rn rs of SO iclentific-research iru3titutli-s and im;tltut ions of higher 'Ar'nIll- evf,r iperF. T'h- ;-'emirv cec--inr w;4E; yearn', pq-A 01.0 it if; ~ri thf, 4rpEj rf pol.yrmf~r 8 v, tha! V. Irl" Of J~-IIVTT:eF -4! q t r e 1/4 ACCESSIC)ii N-R: AP5010235 plan for development of the national economy in 1966-1970. A corre- spond, riigned to thr- produr~tion of eynthetic iijfiv important place is ast fibers. r r 41 -it v 7 T T t r i JS tempe r~;! t. u'i. Thr-.r';l a Z; Rt ri ik.-t ~j T ;4 (acto r q r t- FhPr-P1v i~ 1creases the thermal stability of arorvati.- ~r; T-'' '~I' IrI17--urtinn (') f phenyl groups at the N11 groups of p_p kyt~~nz.i y. i, I z c) 16 iaB no not i c eab I e effect, and incorporation of boron, pho-cphorbs, si it or ferrocene I n)i s ~ir, polybenzimidazole fat-ils to improv- its thermal stability. The high thermal Stability of N-rontaining poj~7nei - the polymellitimide typ- may r-su It frOITI Lh P fOrrT-Iat]Ofl Of StabIC' fr'-P r.,Aic als on heat ing ; I he rrf,. r;4,1 - icals, in turn. promote cross-linking. B. A. Xrentsell Onstitute of Petrochemical Synthesis) discussed ,physiologica1ly acti've polymers, with regard to their synthesis as weU as C.'d 2A to effects of their structure and conformation on their physiological activit-Y, It is de,;irt-d tn reducp tl;eir rroAngenic .,fff-cts to a rn;F-irnum, main- iaining Ir,P,v ,herapeutif- activity. !'r&Yi,--rq cantaini:ig sulfhvJr-,ri and imidazolc groups uffer poteritiall Iu-rij radi.1tion damage. in djsci.ip:~mL7 11asic priberns of th- 4vnt~iesis of polymers which con- I-dr a . -~St(-Tr (if :~- A. R-rll~l I~risWljt( )f Ch( .Cal Phyq'CH) n(Aed the mterusirig, propi-,rLies of Ithis cla-~s of polvi,ers, pLI*"L-,U-&r t"Ie L paramagnetic properties. In h4s pap~-r on the physicocheTrical properties of graft and block co- prlvrners, N. .~.. Platf- irv-l~,Aed i containing rInga in the main chain. T ri V, Card L ACCMSION UP: AP5010235 e1 prepar-1, -At the lyiptitute nf "Jacromoleculai r I)Mp()Lli-(I-R. rClrDt'o;jj;tj'; con- taining perfavalent phosphorus exhibit thr- ',tinh-sl thorri-al st0i Jitv. '-.y n - thesis of fi ber- forming pole ~Ahy a ulfj ~i' c) a43 rt~pw- bN I 7 j% 1- A. Rogovl-, pvesenteO d-ita or. 'hf- groups ;r.1, macron-r)]-' ;-IvJ' and p-raf' ~-polynIPI-3 Of 0111,1108(- 111,j J~())V 0--, A!- pr~ 1(, tl - ASSOCIATIONI SUMITTEM 00 EXCL 1 00 SU13 ODDE: OC, CO IYJ REIF OOC- -C FEB, V. I-Coro 4A VOL40KHINAS A.V.; KORRISKAYA, A.I. Tvanty-fifth conference on macromolecalar compounds, Xbim, volok. no.2t75-76 165. (MIRA 18%6) 1. Veeijoyuznyy nauchno-isoledovateliskiy inatitut iskusstvennogo. volokna. "W".090- =1 I NFi: AP501 65a3 A!7i -)n 6f the bactait if epsilon-caprolact-am and zeta-enanth-1actar, SOURCE: Vysokomolokulyarn-rye soyedinentyu, v. 7, no. 6, IQ,(-II5, 10Q2-1(!f-r7 AB6iltACTV. '."he authurs report Qr, cop,--lymerization of tho hmulhy J'-o-p-rm i n- !-~T),z- (1) wil.h -ind nn n am soyed. ji '-h -.,3 s card 0 L 6298r~-65 ACCE~,' ~T--'N N,11, A P50.1 1 -3 a nri Li Kh idrykr, I Fw)ki Al: -:'R I T (3 hn r ra 7 a .3 9 s ''I r 'All fln a I g "413 jig t -41 I x Tj Is 119 VA A c to VOIDEHINA, A.V.; KUMYAVTSEV, G.I. Polycondeneation reactionx In thip solid phase. Part 2: Solld phase polycondenestion oft -aminoenanthic aqld In the presence of catalysts. Vysokom.soed. 1 no-11:1724-1732 It 159, (MIRA 13:5) 1. Vaesoyuznyv nauchno-issledovateliskiy institut iskusetvennogo volokna. (Heptanoic acid) (Oondensation products) VOLOMINA, A. V., KORYAVTSEV, G. 1*/ SKM'MV) S.- M.' and BONET5KAYA, A..K. (U,1303R) Protsess poliamidirovaniya v tverdoi faze Polyamidatioa reaction in the solid phase iupAc s u:465-71 report presented at the Intl. Symposium on Macromolecular Chemistry, Moscow, 14-18 june 6o. VOrDKH.IN&,. A.Y.; BOGDA1107, H.H.; Y.MYAVTSSV, G.I. Polycondensation reactions in the solid phase. Part 3: F017- condensation of n-aminoalk7lphan7lalkanecarbox7li-- acids in the solid phasn. T7ookoo.ooed. 2 no.1:92-96 it, -16o. ,(MIld'13:5) 1. Vesso7uzn7y naucbno-Isoledoyatel'skI7 institut iskmantvannogo volokna. (Condensation products) (Acids, Organic) VOLOKHINA., A. iV.; KIJDRYAVTSEV., G.I.; RAYEVA, M.V.; BOGDANOV, M.N.; KALMYKOVA, F.M.; OKROYiCHEDLIDZE, N.P. Polycondonsation of diamine salts of terephthalic and hexahydro- terephthalic aelds In the solid phase. Dim. volok. no.6:30-33 164. (MIRA 18:1) 1. Veasoyuznyy nauchno-issledovatellskiy institut iskustvennogo volokna. "CLOKIMA A V. t===:-* "Investigation of the Process of Polyncrization of Cyclic Acatals." Cand Tech 3^-i, I I lbscaa Textilo inst, :!Lii Iijehur Educ.--itlen USSR, Moscow 19Y~- (11, No 1, Jan 55) Survo,,, of ScientUic and Tochnical Dinmertationa DrTendad at, 111('~Ier Educational Instituticus (13) SO: Sm. Do. 598, 29 Jul 55 SKURATOTI SGH,; STRAPIKUYNT, A.A. (deceased]; SHTXKHRRO SM,; TOLOMINA, A.T, PolMrization anthalpy of cyclic formals. Doki. AN SSSR 117 no,?: 203-965 N '57. (MIn 1193) 19' Mookovskly gomidarstvannyy universitat Im, NJ, Lomonosova. ftedstavleno akadealkon A.A. Balandinym. (Entbalpy) (Acetals) 911901621004101210061015 BIOI/B186 AUTHORS: Volokhina, A. V., Fabrichnyy, B. P., Shalavina, 1. F., _J_f ii-E-M- ,~o ~T r 17. TITLE: Polymerization of C-ethyl and C-propyl substituted enantholactams PERIODICAL: Vysokomolokulyarnyye soyedineniya, v- 4, no. 12, 1962, 1829-1832 TEXT: The susceptibility of ~-ethyl-j-enantholaotam and of t-n-propyl-, ~enantholactam to polymerization was investigated. Synthesis: The lactam of 6-(3-aminothienyl-2)-valeric acid# or the laotam of 6-(3-amino-5-methyl- thienyl-2)-valeric acid was obtained from 2t,31-thiopheno-1,2-cyclo- heptan-3-one o~xime or from 51-methyl-21,~kl-thiopheno-1,2-cycloheptan-3-one oxime by Beckmann rearrangement-in the presence of benzene sulfochloride. At the same time the sulfur was eliminated with skeleton nickel, and the double bonds of the thiophene ring were hydrogenated. The polymerization was carried out at,220-2800C with 2~,-H? as catalyst in N 2 atmosphere. 0 Solid, glass-like substances with m.p. 170 C were obtained, which can be Card 1/2 S/190/62/004/012/008/01' Polymerizati6n of C-ethyl and.,- B101IB186 pulled out to filaments at 17*50C and from the hot alcoholic solution of which films can be formed. Th6 polymer yield was more than 991~j the intrinsic viscosity reached 0-50 for the ethyl derivative, and 0.10 for the propyl derivative. Conclusion: In contrast to the seven-membered caprolactam ring, the polymerization susceptibility of the eight-membered enantholactam ring is not affected by substituents.. There is 1 figure. The most important English-language reference is; H. K. Hall, J. Amer. Chem. Soc., 80, 6404, 1958. ASSOCIATION: Vsesoyuznyy nauchno-issledovatel'skiy institut iskusstvennogo volokna (All-Union Scientific Research Institute of Synthetic Fibers); Institut organicheskoy khimii im. N. D. Zelinskogo AN USSR (Inititute of Organic Chemistry imeni N.D.Zelinskiy AS USSR) SUBMITTED: July 7, 1961 Card 2/2 539, 0 90 .3/005/002/008/024 Y6 B10i B102 B, AUTHORS: MidryaYtesy 0, 1.# Mikbayloys X, Vol, okaohievskayat 0. Pe TITLE: Studj of rings oopolymori*zation. ii.Copolymerisatioh of- a-giperidone-with F_~-oaprolaotmm PERI.ODICAL: Vyookomolekulyarnyye.soyedineniyag Y. no, 2 19639 206-411 TEXT: The possibility was studied of obiiining high-m,ole'cular fiber- ----'-f;rming polyamides-on the,baais of oc.-piperidone by.: oopolymeriti.rig it with a -oaprolaotam (CL). ~' Two teohniq-ue''s were applied: t O_ 0 at .40-45004 .1-2 mm ligg CL oonten 8 "9 and at 9000 with-90 and 1000 0Lj (2) in nitrogen atmouphort at 1009.120l,and.16000.,' Th*.oatalysts toed 'were 2.5 mole4, piotaoaium -and, 1..2 moles# N-aostyl piporidon*. Results" with 0 process (1): At'40i^41 0, the polymerizati ,on time.mse 6 hrel at 18-200C 18 hre, the yielde v 6VA)~.Andmqq of thQ copolymers depended on the oomposition and were.-alwayB higher than In the,homapolymers. Mutual activation of piperid6nej"d-_0L was observed, - 'kith i4uimoje64~ar component G~rd 1/3 31190 24 /6,3/005/002/008/07 ii "'., ~PI,01/AI02 copolymeriza On* 40,; Study of ring ratio the*m0pa' deoreinaid-.to" -0 01, so.,that coy8l7merisation ensued at room, tempe-raturs..'. The- maximum yield~vab obtained with-40% Piperidone and 60%, CL. With equlim6lecular component',' ratio,the copolymer contained aqually.. squimoleoular~parts'of the com' roceso (2): -The yiel ponentso, Hedults.ifi.p d increa`Sed:'wI:th~rieing CL content..-,' -C'K-pipeAd6he.in'Atself and its 80-90% mixture, with Ct-oould`n6t be' polymerized under'~_Ahis~, QOnditions. The 0 1 , t m4p.., of .,the cop ilymer' noreased with inoreas ng CL con eilt, The oRtimus yieldo 97~a, was obtained with .36A. piperid6pe +,.1760- CL. The polymoVisa:tion' 0 ti~a6- was r OOG' 2 hr 0 9 '1~ hr'-at A h;s:at.-IO s "at -~ 12 09 16o c. Th melting PC_ a a with 'i' A'zai i On I -t e incre so'' . Ir sing polym r mpers, ur an&reache: -185 C- The. ri6leouldr veight, is'not. ikf feated,by, varyi, ng~:the addition,of potassi~a. -between flanld.'2i~ moleop W.fit ~ Is''redubed when 'the(addition vfl-acetyl 1~)iperidone is.increased frbm'_O'~25 to 1 At rv'i 05001 ~ a fiber was drawn- fr olym-eit. melt'having, an intrinsic' 'vinobsity*o 0a6v which om the '6o)p had 460~-506~.' si6iig~tioh-,a"t ro66 tomps*atlirq. -,The* Ancrea'se in'. r.eA.ctiVity .. of the,~a-pipei$done i~ the. AL is due . to thermo-" oynamio and,kinetio partioular;Ltiao-of,tho.'vrooioso which must be furthst invest igate.d.* 'There. are','4 figured and 1 tablee. The most.important. Engliah-languagg'reforenc6'ia*. "-Ni. j0 da', k...Mijako J-, PolYwr Scies 43 s'. 117i+ -960 ~-,Cj~rd, ~2/3 9/190e$3/005/002/008/024 of Study ring & oopolymprization. .. BI 01 02 , . , . ASSOCIATION: vEif..ooyuznyy.,nauohno'-isoledovatel.inkly institui itikusstvannogo,volokna (Ali-Union,ooientifio'Researoh. Illatitute of Syn thatio Pibers SUBMITTEM Jilly 28t,, 3/3 LEVITF.S., E.I.; VOIA)KHIJU, A.V.; KUDRYAWSEV, G.I. Solid phase polycondshoation reactions. Part 4; Solid phase copoly- condensation of amiii acids and diamine salts of dicarboxylic acids. Vysoksm.soed- 5 no.6:875-8~80 Ja 163. (MIRA 16;9) 1. Vsesoyuznyy nauchno-issledavatellskiy institut iskusstvennogo volokna. (Amino acids) (Polyamidas) (Polymerization) 'A, A. VEV~Ibrlwu oymerization of cruc formals, Strepikhtcr Rud A. V. Volokbitta. Daklady, Meg. Napil 141 S.S.S.R. 99. 4G7-l4X-IW4)~--Tftb*tmcnt of cyclk: formals Ittivethylenc, tar=ethylene, 1-methylethyleft tetrasylethylbelixylidene, perstamethyleac) with 0 25% cam- apid pol;~~erlra'lun t'llarulIM1114 acid Ll cRtalyst 16tds to r, to a Ifficar t4l)-mer. llie reitsks show that the stability of cyeffe fanu2N decrames with &.i no. of tist-mben Its the dng OntheorderM0,11. lacrm" of temp. shifti the polymer- monomer tquii. toward the munxiter, whIP! Win. farm the -1 monctnerlpolyntre In iwife rendt. The wt. proportion c 11 It Indepe :yclI, tomals cli adent of Use usol. wt. -Thrr 4 e Xt t-glymerize In the alt-mismof a catairt..-.0y, ht 07 o V( go /0 oo Y/0 111 /0 2 G 0 /B061 AUTHORS: Volokhina, A. V., Bogdanov, M. W. K,idrya-tspv. G- 1, TITLE. Polycon4ensation React iort,311ri thri "Mlid PrAje_ 111, Polycondensation of p-Aminoalkyl -phony'. Aitrin- Acids in the Solid Phase PFRIODICAL: 7ysokomo1eku1yarnyye 11460. V~11, pp, 92-96 TEXT: The authors previously described the synthetii, cf o-,arbGryl~.!~ acids of the genoral formula'H2N(CH;,,)m(C(,H,4)n'CH-,)nCOOH (m - ',2. I n z 1~29394) and their polycondenastion (R-rA. 1,21, The kini!ti-~i of the poly*condensation of the following ncj~31ii ~-xamined here; p-aminemethyl-phen,yl propionic acid (11): valeric acid (IT); p-aminoethyl-phenyl aceti,-, a,~,,id (111): propionic acid (TV); p-aminaethyl-p~-,Mv'. ethyl-phenyl valeric acid (VI). The kinetic,3 of tb.) Were Card 1/5 829BO Polycondensation Reactions in the Solid Phase, S/190/60/00?/01/11/02! II!. 11olycondensation of p-Aminoalkyl-phonyl B004/BO61 Al;(,r-io Carboxylic Acids in the Solid Phaae obaorved during the reaction by oontillU011A woighing, and the degr-~ of polymerization was established by dotermination or the separat9d 4alqr, Fig. I shows the kinetics of the polyconde-nsation of the ab,-,11+,, ,emp-jund.3, and Table 1 gives the experimental data. It follows from thii tiria~ the initial temperature of polycondensation falls with sinking milting point of the amino acid and with increasing content of methylene As regards p-aminoethyl compounds, the temperatur- rRngp between -ie initial temperature of the polycondensaxion anj the rn~?Iting p,)jrt thp acid decreases with increasing content cr,metbylene groups and with decreasing malting point of the acids This connection was not obseryvd in-methyl-substituted compounds With increasing content of' mothylene groups, the polycondensation reacrion rate increases, Fig~ 2 shows the change with time of the degree ef polymerization of compound (I), which is not linear. Table 2 gives the activation energies for the poly- condensation of compounds (I) tc (VI), There are 2 figures. 2 tablqsi and 4 referenoes: 3 Soviet and I US? Card 2/3 Polycondensation Reactions In the Solid Phase~ 3/190/60/002/01/71/071 111. Polycondensation of p-Aminoalkyl-phenyl B004/BO61 Alkane Carboxylic Acids in the Solid Phase 82080 ASSOCIATIOH: Vsesoyuznyy nauchno-isa1.?do--,ato1-v.Kiv init4to% iskusstvennogo voloknr% ( A1 I(5w i (,i, i k- ni t' ifit~ Ft r t h Institute of Synthetie~ F-bors) SUBMITTED; October 9, 1959 Card 3/3 S/063/62/OG7/Gr.'2/0C3/0' '. A057/A126 AWHOR. V21okhina,--A.Vj- Candidate of Technical Sciences TITLE: Synthesis of polymers by opening of ring PERIODICAL: Zhurnal vsesoyuznogo k *himicheskogo obshchestva Im. D.I. Mendeleyeva, v. 7, no. 2, 1962, 140 - 146 TEXT: A short survey and discussion of new methods of polymer synthesis by ring opening which are not cited In other reviews already published is pre- sented. Polymers are discussed in groups related to their chemical structure (polyesters, polyamines, polyamides, polysiloxanes, and inorganic polymers). Chiefly are cited investigations by western authors. Polymerization effected by ring opening and formation of linear polymers is of importance for the produc- tion of synthetic fibers. This reaction is also of special theoretical interest. According to A.A. Strepikheyev's theory, polymerization of heterocycles may be particularly important in biological formations of high molecular weight com- pounds, since chain polymerization, or polycondensation are not probable in liv- ing cells. Polyesters can be obtained by polymerization of cyclic oxides, or lactons. Of special interest is the solid-phase polymerization of the latter by Card 112 Synthesis of polymers by opening of ring S/063/62/007/002/C03/014 A057/A126 ionizing irradiation. Copolymerizations of cyclic oxides, or carbonates were carried out recently for the first time. Polyamines can be manufactured by po- lymerization of cyclic imines, or cyclic urethanes. Polyamides were obtained generally by polymerization of lactams, which processes are of Interest for the problems of albumin synthesis. Several organocyclosiloxanes with different sub- stitutes at the silicon atom were prepared and studied by Soviet investigators. The latter observed the effect of the substitute on polymerization degree. Among inorganic polymers are mentioned by the present author polymerization products with sulfur, zelenium, and the rubbery polyphosphonitrilochlor-ide. GG;1- cludinG -rhe present review 'the author states that It was possible to effect. pe- lymerization of cycles which were considered before as not polymerizable, such as paraformaldehyde, ci.-pyri~ol3.done,r,~-piperidone, etc. Principally, any hetero- chain polymer obtained by polycondensation of bifunctional compounds can be pre- pared by heterocyclic polymerization. The latter is, therefore, of particular Importance for the development of polymerization processes. There Is I table. It Card 2/2 __12!!qK~HIN -.AJs-.kand.tekhn.nauk Synthesis of polymers by ring opening. Zhar.VKHO 7 no.2:140- 146 162. (Polymers) (KRA 15:4) a. VOLOXHI IIA, A. V. Water content at equilibrium of the vapor phase of the system poly- jE -caprolac tam - water. Xhim. volok. no.2:16-18 '59. ( KRA 12; 1,.Veaeo7uzny7 nauchno-isoledovateltaki3r institut iskusstvennogo volokna. (Hexamethylenimine) (Systems (Chemistry)) /15T 66961 SOV'/183-59-5-3/28 AUTHORSi Z.01 o~4~yko,,,..A,,.,S.,tjldryavtoev, G. I. TITLEt PolycondeneationlReactions in the Solid Phase. Communication 1. Polycondeneation of Aliphatic w-Amino Acids and Diamine Salts of Dicarboxylic Acids in the Solid Phase PERIODICAL: Khimicheskiyevolokna, 1959, Nr 5, PP 13-18 (USSR) ABSTRACT: The authors investigated the general rules of polycondencation in the solid phase by means of three w-amino acids (amino- enanthic acid4 aminopelargonic acid, aminoundecanic acid) and the hexamethylene-diamine salts of the adipics terephthalic, and thiodivalerianic acids. The temperature dependence of the reaction was observed by continuous weighing during thecondensation process, and by measuring the quantity of water separated out. It was shown that the reaction takes place within rather umall temperature ranges 6-15 00 near the melting point of the ini- tial and end products, the temperature coefficient of the reac- tion rate being rather high. If the three amino acids are com- pared with respect to the reaction rate o.11' polycondensation at the same temperature, the aminoundecanic. acid reacts most rapid- Card 1/2 1y followed by the aminoenanthic acid, the aminopelargonic acid 66961 SOV/103-59-5-3/28 Polycondensation Reactions in the Solid Phase. Communication 1. Polycondensa- tion of Aliphatic w-Amino Acids and Diamine Salts of Dicarboxylic Acids in the Solid Phase being the slowest. With respect to the activation enerpy, the acids show the same order beginning with the aminioundecanic acid as the consumer of the least energy. As to the polycondeneation of the hexamethylene-diamine salts of dicarboxylic acids, it was shown that the higher the melting point of the ealt is, the higher will also be the temperature at which the reaction starts,, and the vider the temperature range is within which the reac- tion takes place, the lower will be the temperature coefficient of the reaction rate. If the reaction takes place in the solid phase in open vessels at higher temperatures, hexamethylene di- amine will be separated out and, thus, excluded from the reac- tion. In this way, the reaction equilibrium is shiftad to the effect that a formation of higher-molecular polyamidez is not possible. The same applies to the reaction in the liquid phase (melt). There are 5 figures, 4 tables, and 10 references, 3 of which are Soviet. ASSOCIATION; VNIIV Card 2/2 5 ( 3.) OY/-0-127-6-21/51 AWHORSs Volokhinaj A. V.jjCudryavtsevj G. I. S TITLEs Polycondensation of the w-Aminoenantiap t-3-Aminopelargoniop and w -Aminoundecanic Acids in the Solid Phase PERIODICALs Doklady Akademii nauk SSSRO *1959, Vol 127t Nr 6, pp 1221-1224 (USSR) ABSTRACT: The polycondensation of some bifunctional compounds can be carried out, according to data in publications (aefs 1-5), in a solid state. This reaction has, haffeverp not yet been investigated eystematically. It is, howeverp of high theorotical and practical importance, particularly if the monomerag and the polymers obtained from thempare insufficiently heat-resiotant. Besidesi the said polycondensation apparently represents a bazic method of producing polymers which are not fusible, or fusible at high temperature under decomposition' e.g. polyamides containing aromatic or bydroaromatic rings (Raf 6) in the chains of the macromolecules. The amino acids mentioned in the title were made of totraohloroalkanea (products of telomerization of 6thylene with C01 , Ref 8). Pisure I shows ilyaondensation process. From the values of the curves of the po Card 1/3 the polymerization degrees of the polyamides determined from the Polycondeneation of the ci-Amincenantic, SOV/20-1~7-6-21/51 c4 -Aminopelargoniog and W-Aminoundsoanio Acids in the Solid Phase nufter of terminal groups, as well as from the polymer yieldat the water quantity can be computed which was separated from a ocrtain quantity of amino aoid..k comparison of these quantities with directly measuired (weighed) quantities is shown in table 1. The reaults~obtained demonstrate that: I)-the polycondensation mentioned in the title Proceeds at a considerable rate within a rather narrow temperature range (6-150)1 these temperatures lie near the melting-.points of the said amino acids (bY 5-200 deeper) azid-of the polyamide' corresponding to these acids (by 8-500 deeper). 2) The rate of this reaction has a very high temperature coefficient 3) The duration of polycondensation in the solid phase at 1840 must be 18 h at least if polyamides are to be obtained from the aininoenantic acid with a specific viscosity requ ired for the formation of solid fibers- 4) It is not possible to compare the polycondeneation rates of the 3 mentioned amino acids at the same temperature since the temperature ranges of the polycondeneation of the 2nd and 3rd acids are different. If the usual kinetic method is applied to Card 2/3 describe the reactions Lin the solid phaset the data indicated in Polycondenzation of the c,)-Aminoenantict BOY/20-127-6-21/51 4j,-Aminopelargoniol and w-Aminoundecanio Acids in the Solid Phase table 2:and figure 2 are obtained in the computation of tht effective activation energies of polycondensation. According to thevalues-of the aotivati-on energyp~the acids under consideration can be placed into a seriest aminoundeoanic acid 4 aminoonantio acid /, aminopelargonic acid, This series has no relation to the chemical structure of these acids. As is expected, the activation energy falls rapidly in the presence of a liquid phase4 There are 2 figures, 2 tablesp and 9 refordnees, 2 of which''are Soviet. ASSOCIATION: Voeeoyuz4y~y hauchno-iseledovateliskiy institut iskaostvennogo volokna (All-Union Scienti.fic Research Institute of Synthetic Fibers) PRESMEDz April 15# 19599 by V. A. targin, Academician SUBMITTEDs April 8, 1959., ~Card 3/3 )UKHIWV, N.V.; SHABLYGIN, H.V.; VOLOMNA, A.V.- Mutual effect of sonomers during their copolymerization. Vysckcn. soed. 5 zo.11:1757 N 163. (NIRA .17:1) Vol-OKV11rills F).V. SMWIMMYXT, A.A.: VOWMIYA. A..T. ~ _ Squilibrium polyzerlution of cyclic formalss Do,kI. AN SSSR 99 no.): 407-410 1 154. (MLRA 8:2) 1. ]Pro&stavltno akadeatkom, I.L.Knurwantses. (Polymers and polymorlsation) (YbOwlal) VOtMINA, A. V. 1447 losledovaniye protsessa polimerizatsil tsikllcheskikh atsetaley. M., 1954. 14 s 22 sm. (Y,-vc vyssh. obrazovanlya SSSR. Mosk. tekstilinyy in-t). 100 ekz. h. ts.-(54 3 719) SO: Knizhaya Letopis', Vol. 1. 1955 -M IMAM. ~,Y, ERT wa OL-C>K)4 K\ A UssRAhemistry Polymerization ardlA Pubs 22 -18/40 Authors I Streplkheyev,, A*Aop,and Volokhina, A V* Title Equilibrium polymerization of cyclic formals 'Periodical s Dok. AN SSSFt 99/30, 407-4200 Per 220 IL954 Abstract 4- The state of the following, system wall investigated at 100-15&.and 10-100% -.-benzene solif;ion:concentmtionst-.monowar _ polymr (polymerization equili- brium) for ethylene-, trimethylene-o tetramethylene-j, pentamethylens formals- (~,6-o 7- and 8-membered c7cleB)j tetramethylenebenzalp 4-methyl-1,3-dioxans and dimeric 16-membered pentamethylene formal. The only chemical process observed during polymerization of cyclic formals was the redistribution of hetero-bonds in space,ard the conversion of cyclic bonds into l1near. A close connection was established between the stability of cyclic formals and the number of members in a given ring* The effect of temperature on the monomer polymer equilibrium is explained. Eight referencest ~-USSR; 1-Swiss; 1-French; 1-Oarmano-U930-1954) Institution s 00*0 Presented by i Academician I.L. Knunyants, Jww 23# 1954 L -6 WP(J)AW(M)1BDS ASD Fb-4 RM CCESSION NR: AP3001160 510190163100510061087510880 AUTHORt Leyttes, 9, Ij,; VQlokhina, A. V.j Kudryavtaev, OC-14 TITLE: Solid phase polycondensation 4. Solid phase copolycondensation of amino acids and the diamine salts of dica% lylic acids SOURCE; Vy*sokomolek-ulyarny*ye Boyedinaniya v. 5, no. 6, 1963t 875-880 TOPIC T&GSs polycondensation, eopolycondensation,.amino acids, diamine salts, dicarbo.Vlie acids, copolymers ABSTRACTs The present work is a continuation of earlier investigations by the --authors. It involves the study, by th etrio method of the kinetics of co- .Poly ndensation of four pairs otj 0 de foming monomers, namely, aminoonanthic AAcdTAA) with hexamethylenediamine a HDA), piperazine adipate (PA) with p-minoethylphorqlpropioni t a thylenediazine adi to (HDA) with the decamethylenediamine salt of hexahydr-oterefthalic acid (DDHdIr TA , and hexa- methylenediamine adipato-(HDA) with hexamethylonediamine isophthalate (HDIP). The basis for assigning a particular amine to a specific pair hinged on closely matched -rates of polycondensation at -the same temperature. The end products of the reac- tions were solid masses, which readily disintegrated into a powder. It was found Card 11A2- ..................... ......... ....... ................................... L 12423,63 ACCESSIONM AP3001160 -that at 15600 the polycondensation of A and HU partly proceseed in the malt phase, the actual melting point of the mixture being 172-173C. while that of its --.-----consti-tuents--is-193-194C.and-1950- -For-PA and PAP?,.-the homopolymers of-which-are practically not fusible..the reaction proceeds via melt at a temperature exceeding .235C, and for HDA and DDHTA.at over 156C. The copolycondensation process for NU and HDIP in a lil ratio proceeds at 169C in the solid phase, and, having reached 62% of its total potential, it practically stops there. It is assumed that only HDA reacts at this point, which is -confirmed by analysis of the resulting poly- condensate. The composition of the obtained polyamides was studied by means of chromatography, and their solubility in various solvents was Investigated. It was -found that the ltl copolycondensation product of PA and PAPP was soluble in tri- cresol, while none of the constituent homopolymers were* The chromatographic Jm- vestigation of the.copolycondensation products revealed their structure as that of copolymers with a statistic distribution of monomerio units. This was established -for the AA and ADA as well as HDA a nd DDRU copolycondensation products. It is iconcluded that the reaction under investigation yields a true polyamide and not a mixture of homopolyamides. Orig. art. has: '5 charts. ASSOCIATION:- Vsesoyuzrq*jr nauchno-isolodo-vatel I akiy Inatitut lakusstvennogo ,volokna (All-Union Scientific Research Institute of Artificial Fibers) :Card '21A 4-41 .4 k, . . ... . . . . . . . . . . . . VOLOKIIINA A.V - FAIMICIINYY, B.P.; SIIAIAVINA, I.F.; GOLIDPARB, Yu.L. Polymerization involving ethyl- and propyl-sub--tituted onantholactains. Vyisokom. soad. 4 no.12il&19-181~ fj 162. (1-URA 15:12) I. Vaesoyuznyy nauchno-isaledovateltakiy Institut, iskusstvennogo volokna i Institut, organichoskoy khimii imeni, N.D. Zelinskogo AN SSSR. (Azicinone) (Polymerization) VOLOKHINAs A*V.,; NUDRYAVTSEVs G.I.1 MIXUAyWVs N.V.j ROXACHMKATAp O.F. Ring copolymerizatione Part 1: Copolyzerixation of 6c-piperidme vith ~--caprolactam. Vysokom.soed. 5 no.2t2O6-23.1 T 163. (MM 16t2) 1. Isesoyu=yy nauabno-iseledovatellskiy inatitut iskusstv=ogo vololma. (Piperidone) (Azapinone) (Pblymerization) I L~AQ98-65 EPA(s )-9kWT(M)/EPF(C )/EPR/'F'W-P(J)/T Pc-qf;2 4# A'- lfl N' A.. A-71i"14! PokachevskVal 0. 1 q TITLF Preparative methc~, f-)r heat-resl an'. '.yttm~ ~o~s. Class 39, go. 168434 izobreteni- i t,,iarnykh zna~rov SOURCE: Byulleten' 1965, 61 TOPIC TA";S - rnlyami(le, h-sit resistant p,-.)lyqmiJe, lar-tRm Aji Authorcertif~~ate has been issued for a preparative method for heat- resi,'~inli L,olyamidesNased on hexahydro-p-aminobenzolactem. In order to increase the mo 'e,ular weight of the poLyamides anc, g've them F'ber-forming proper'~ies, this iactrin iF: o,)pcly-merj7ed vith other laclrm&, surh as c-caprolactam or E-enantholactam. [SM, J L ASSOCIATION: Vsesorlzny-y nauchno-issledavatal'skiy instItut iskustvennogo volokna (A,';-''n. n ~rientific-'Flesearch institute -f Man-Made Fibers) ~11 T on ~lllu - Z -M NO REF SOV: 000 OqFER. 000 ATD pREgs! 3 2 10 Card I /I VOLOXHINY A. YE. 42523.- Sredfieratochnyye arterii I diagnostr!ka arokov stallnosti U Korov. Veterinariya, 1948, No. 12, S. 34-40. 0 ~ BABICHIV, P.S.: VOLOM~&JOJU "mom, , InterArtion of 3-methyl-2-ethvlidmnebenzothiazollne with halo deri- vatives. Ukr.khtm.zhur.17 no-5:761-765 151. (MW 9:9) l.Kiyevskiy gonudArstvennyy universitat. (Dennothiazoline) (I[Alides) 0 SARIWVAp X.P., dotsentj ~RLCK~Mj KONAKHOVA, M*A* Diapostic olpificance of various J=unological factors in rboumatio favor in obildron. Pediatriia 39 no,207-42 F 161, (MIR& 140) lo Iz fakifl'totakoy torapovtialiegkoy kliniki leallobnogo fakull- tota (zavo - doystviteltnyy chlen Mi SWR prof. A.I. Nesterov) i fakulltetskoy detskoy kliniki (zav, - prof, P.A. Ponmareva) 11 ffbakavskogo maditsinskogo instituta imeni N.I. Pir ova* (HIMUMATIC FEVER) (ANTIMOLYSIN) (HYAUJRMIIDG5 VOLORB-ISAYEVA ym.N. Treatment of late pregnanc7 toxemlas. Sov. ned. 28 no-3272-75 Yr 165. (MIRA 18:10) 1. Kafadra akusherstva i ginokologii lachabnogo i atoiratologicheskogo fakulltetov Tanhkentskego rneditsinskogo inatittita (naucimyy rukovoditell Prof. A.A.Kogan). VOLOK]IOTIOVICII) I.Ye.; MAROVICH, A.M.; MASTEROVOY, I.F.), AZATIMI, V.V. Nonisothermal processes. Thermal cracking of metbane. DokI. All SSSR 146 no.2:387-390 S 162. WILI 15:9) 1. Institut khimicheskoy fiziki, All SSSR. Predstavleno akademikom N.N. Semenovym. (Methane) (Cracking process) _2244 3v 66__-rYr(m)/Fwp(j) _1JTP_(-c)__WWJ11L_ CC NRt AP-60676j60 7 (A) SOURCE CODE: UR/0413/66/000/002/0095/ AUTHORs Pashchonko, Do 1, ; VtorXgin, S, M, 0 KISX!~enov, N. A. Harkevich, 1, M,; VolokhonovichL 1. Ye.; Nosov, E.. F.; Zoifna. L . 11. ORG: none q, I-TITLE: Preparation of polytetrafluoroeth%lpnel Class 39, No. 178104 [announced by Institute of Chemical-Physics.-AN S55BLS(Institut .khimicheskiy fiziki AN SSS.R)l SOURCE: izobreteniya, promyshlennyye obrazt0y, tovarnyye znaki, no. 2, 1966, 95 TOPIC TACS1 _ poly te traf luoroe thylene I polymerizationp polymerization initiator ABSTRAC i method of preparing polytetrafluoroathylene through pqjy: __Teriza.tlonIof tetrafluoroethylene under ultraviolet light in the presence o initiators is described. In order to obtain polymers with an extensive outface area, perhalogenated freons are proposed for use as initiators. (LD) SUB CODE:,071 Card UDCs SUBM DATEe 22Feb65/ V014KHOSS I KA, L. I. Iffect of histamine and digestion on the metabolism of phosphorus compounds In the gastric mucosa Lvith summary in Inglish]. Uicr. blokhim.zhur. 29 no.1:101-108 157. WRA 10:5) 1. lumtitut blokhImij Akademil nauk Ukrainelkoi RSR, Kity. (PHOSPHORUS KATABOLISM) tHISTANIU) (DIGISTION) VOLMONNAYA, L.I. [Volokhonolka, L.I.) Metabolism in the gastric =cows during prolonged starration. Ukr. b1okh1m.zhur. 30 no.3t441-450 '580 (MIRA 13:3) 1. Institute of Biochemistry of the AcadsvV of Sciences of the Ukrainian S.S.R. 11yev. i'STARVATIOW) (STOPAGH VOLOK11014SKAYA, L.I., kand. b1olog. nauk; MEZIOUNA, Yo,P.p kwid.med. nauk. Charaotoristics of some aspects of phozphoruz and nitroger. metabolism in patients with cerebral spastic paralysis. Trudy Ukr. nauch.-issl. inst. ortop. i travme no.15:73-77159 (MIRA 16:12) lo Iv Kiyevskogo nauchno-ii3oledovatellskogo instituta ortope- dii i travmatolo ii (dir. - laureat Stalinskoy premii K.M. Klimov (doceasedj). VuLCKHul-l'3K,lYA, L. 1. "Data on the Study of Metabolism in the Mucous Membrane of the Storniach.11 Cand Jiol Sci, Chair of diochenistry) Kiev SuAte U imeni ~. G. Shevchenko) Min Higher .-/Jucati~m USSR, lr~ievp 1954- (il, No 8,, Fef) 55) SO. Sum. No. 631, 26 Aup, 55 - Scurvey of Scientific and Technical Dissertati,,m Deft:nded at USSR Ifilgher i;dilcational Institutions. (14) VOLOKHONSKAYA M,L.; VORONKO, N.D.; VYSHESLAVTSEV, S.I.; YAROSHEVSKIY, F,Yu, Reoulto of somicarbaside-cadmium therapy in patients with malignant tumors in incurable stages Vop* onke 9 no,6:92-104 163. (MIRA 17-- 8) 1. Iz polikliniki NO-3 AN SSSR (glavnyv -irach - D.I. Sherstnev, a 1958 9- - I.A. Strunin, zamestitell glavnogo vracha po lechebnoy chasti - N.P. Vasillyeva). Adres avtorov: Leningrad, V-164, Universitetskaya naberezhnaya, 5, Poliklinika No-3 AN SSSR. (Cho, Prom experiencA- w-Ith in Chernovtay I~rmldrlor. Sov. 110-3t5,

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