SCIENTIFIC ABSTRACT BELSKIKH, V.I. - BELSKIY, I. F.

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BSLISKIKH V I kandet6khnrAUk Automatic temperature regulator. Avto prom. 27 noo 5:19-20 My 161o (MIM 14:5) 1. Visesoyuznyy nauchn6-issledovatellskiy institut makhanizataii sellskd~b khozygLystvao (Temperature regulators) BELISKIKH, V.I,j kand.tekhn.nauk- Efficient cooling system for internal combustion engines. Avt.prom. 27,no. 6&34-17 je 161. (MMA 14:6) 1. Vsesoyusnyy nauchno-iseledovatellikiy inatitut mekban4sataii. Bellskogo khozyaystva. (Motor.vebicles--Engines--Cooling) S/262/62/000/008/014/M2 IM711207 AUTHOR~ Bel'skikh, V. 1. TITLE: Suitable cooling system for an internal combustion engine PERIODICAL: Referativnyy zhurnal, otdernyy vypusk. 42. Silovyyc ustanovki, no. 8, 1962, 56, abstract 42.8.300. Avtomob. prom-st', no. 6,1961, 14-17 TEXT: The author devised and experimentally chocked a water-circulation system ensuring thermo-siphon cooling of cylinder liners for the case of forced cooling of the combustion chamber. The proper operation of such a self-adjusting system requires even distribution of water supply to each chamber and uniform hydraulic head; uniform arrangement of parts linking the block jacket with cylinder-head jacket to ensure even distri- bution of temperature in the circumference of the cylinder liners; arrangement of the water outlet connection above the cylinder head thus ensuring convective heat exchange between the water within the block and that circulating through the cylinder head as well as the absence of steam pockets. There are 4 figures and 4 references. [Abstracter's note: Complete translation.] Card 1/1 PASECRNIKOV, N.S., kand. tekhn. naukj__4U_~SK;KH, V.I., kand. tekhn. nauk; YALOVENKO,, F.I.-p-RA-n-d-.7T-ekhn-.-NMwT-- KASPEROVICH, V.V., inah.; VASIKOVSKIY, S.Ye.p red.; GRISHIN, L.V., red. (Technology of the maintenance of the "Belarus'" traktorb) Tekhnologiia tekhnicheskogo ukhoda za traktorami, "Belaruel,n Moskva., Biuro tekbno informatsiij, GOSKITI, 1964. 298 (MIRA 18: z 1. Perovo. Gosudarstvennyy vsesoyuznyy nauchno-isoledovatell- skiy tekbnologichaskiy institut remonta i ekspluatateli mashinno-traktornogo parka. 2. Goaudarstvannyy vseaoyuznyy nauchno-isoledovatellskiy tekbnologicheskiy institut remonta, i ekspluatataii mashinno-traktornogo parka (for PasecbnJkovp Bellskikhj, Vaslkovskly). 3. Gosudarstvennyy soyuznyy nauchno- issledovatellskiy traktornyy institat (for Yalovenko). 4. Minskiy traktornyy zavod (for Kasperovich). BELISKIXHP VoL ka.nd. tekhnonauk; BAGDASAROV,, N.V., Inzh. Determining the~loading degree of an engine by means of an electrio- light signaling mechanism. Trakt. i sallkhozmash. no,3:11-13 Mr 165. (MIRA 1&0 1. Gosudarstvenn*yy vsesoyuznyy nauchno-issiedovatellskiy tekhnologi- cheskiy institut remonta i ekspluata-tsii mashinno-traktornogc O&pk&4 (for Belittkikh), 20 Vaesoyuznyy nauchnc~-issledovatellskiy institut mekhanizatsii seltakogo khozyaystva (for Bagdasarov). MIKHAYLk. M.-, SINUSHAS. A.; HILISKIS, V., mekhanik; BALITRUSHAYTINE, B., kontrollny7 master. Advanced methods used in manufacturing asbestos slate. Stroi.mat, 3 no.11:14-16 N 157. (MIRA 10:12) l.Daugelyayakiy kombinat stroitellnykh materialov. 2. Glavnyy inzhener Daugelyayskogo kombinata stroitelInykh materialov (for Mikhayla). 3.Nachallnik shifernogo tsekha Daugelyayakogo kombinata stroitelinykh materialov (for (Sinushas). (Daugeliali--Asbestoe cement) BELISKIY, A,., kontr-adairal zapaaa On the batt3- watob. 'roan. 2nan. 38 m.10:4-5 0 162, (14IR& 15-10) Russia- (Cmmunist Youth Lea gue) p ". II N ~ -IV ,Z:~, IS, ~ , ~y I ~ BILISMY, A., insh. Slaughterhouse became a meat combine. Rias. ind. SSSR 28 no.6.#34-35 '57. (MIRA 11:1) 1. Glavny7 inzhener Melovskogo mvasokombinata. (BIblovo-Phoking houses) BZLI SKIY.. A.,--,- Maldng foremen responsible for technological control. Mias. ind.SSSR 30 no.1:22-23 '59. (MIRA 12:4) 1. Belovskly myasokombinat. (Heat industry-QuAlity control) .MMISKIT, A., inzh. I Redesigning tho "MookviCh)m" saw. Hias.ind.SSSR 31 no.1:51 '6o. (MIRA 13--5) 1. Belovskiy mrasokombinat Kamerovskogo movuarkhoza. (Belov-Packing houses--Zquipment and supplies) 11 IJBLISKIr, A. Mobile platform for the unloading of cattle from railroad care* Mias,- ini. SSSR 33 no.3:46 162. (MIRA 15:7) 1. Yeletskiy ptitsemyasokombinat. (Cattle-Transportatibix) (Ioading and unloading-Equipment and aupplies) BZLISKIT, At A* 32677, Zkopertmentallwya provorlm uslovly Ilky1distall vygreboy v royous, stroltellst novoy lumnalizateli leningrada. 4&klad na konterentmile sozve naveh*-Issled. In-Som tmumle Ihozyaystva ispolkoma longorsoveta. Kay 1929, 0:7HAterialy pokommunal. Khoz-yug 19499 SB* 3o me 67-72 801 Letoplel Zhurnallafth Statoy, Vol. 44. Moskva, 1949 T.G.; IMLISKITI, A.A.; SHCHUPANOVSX&TA, R.r. Characteristics of magnetic fields of drum separators with closed circuit. Obog. rod. 3 no 03:26-32 '58. (HIR& 12:1) (Yagnetic separation of ores) EELISKIY, A.A. CaleiLlati~g ~hs susceptibility of open magnetic systems in ~.separators. Obog. rud 5 no-3:42-4 160. (KM 14-18) ~ tMagnetic separation of ores) BEL'SKIY*-..A.A.- . II Calculation of permanent magnets in magnetic field patterns. Obor rud 5 no.6:41-44 160. (KIM 14:8i (Magnets) EELISKIY., A.A. ..HigUy..ef.ficient.rfiapatic,is-sparators. Obog. rud 6 no.3:41-43 161. (ILTRA 14: 1-1) (Magnetic separation of ores-Equipment and supplies) C~11~-z".i~zM-IM-dMI --7 ---r BELISKIY~L,k.A.LMYSUMOVAP Hope Ceramic magnets made of baritim ferrite. Obog. rude 8 no-3; 30-32 163. (MIRA 17--l) U 8 S R MtAtt-. ~ZA&,L, Tc"; t i;i- c ' 11 ~.t 1934. 2k (3). 8211-8 R",.' - hj. it 6 onfir w,,l I &ymft""~s e"me vxtlficat-"~~'. rl!' Go= thiLt with Ii :Sa %;epirm. However. Qf high r"twu-a tho C*--M of reat'la(miall >' It), w r%% tlo syewm w of ao pma!j"I haportallea: Other experimsiqta witil tho voatApt arrungod in the crdtr Mmt,-l (2) pyd t~o fallowkq mtulta; (1) Appr.. of lia, Hg to-Sa to makn lig,"-w tivcA Mt',tler cmdiwtivity. b'a no 6AEer motiL.-ail3n thail if is aj,;lled from vapwr. thermal of tho So. (3) &UT.C.. at the evilta'at Vcu. (1)1~3* i4 ewIlAxable in 'mr.*pitntl(i 44,tls th%k it tl4e- &jjlg&- al;u 'ai~ 1u C Awl A). 41 frXC41CMtX4# A; IfAA tillue t , ~s h-A f.uparlm71%, VIQ WZAL tX'r 'v cl idTij !y rt kt~'4'td Wy (NI, a TZPXRMAN, Yefim Yakovleiich; BELISKIY A.M., otv.red.; LIBMWN, S.S., - i ='- ~-- ' ~-7 I- red.isd-va; ANDREYEf, S.P.. tekbiii6d. (Mine dewatering pump; a manual for schools and training courses for mine foremen] Rudnichnyi vodootliv; uchabnoe posobia dlia shkol i kursov masterov. Kharikov, Goo.nauchno-tekhn.izd-vo lit-ry po chernoi i tavetnoi metallurgii, 1959. 151 p. (MIRA 13:9) (mine pumps) (Mine water) iA. ectricity - So.iconductors G-3 Abs Jour Ref Zhur - Fizike, No 3, 1957, No 7006 Author -Bel-I skiy, A. S. Title Froceduro for Moasuring the Electric Conductivity of Di- electrics and Semiconductors Using Fulses in Strong Electric Fields. Orig Pub i,Uch. zap. Tor-skiy gos. pod. in-t,-1955, 14, 535-539 Abstract The author considers a nothod for measuring the electric con- ductivity of somiconductors with the nid of rectangular pul- ses of 10-3 -- 10-5 see duretion. The generator is a cethod6- coupled multivibrator with one steble state. The resultant pulse wrs.first r-mplified with r single totrodo stage, The loed was the invostigrted spociron (RO; CO) and P stnnderd resistence (Rt) connectect in series with it. By verying the capncitence C in Farrllol with R,t, the condition RstC = R0Co. In this case the wavefor--: of the output pulse acroes the lower and of the divider (ecrosE R ) does not become dis- torted. The voltego in -casured WIth on oscillograph. Card 1/1 BELISUT, A.Vo, dotaent, Prevention and surgical treatment of relapses of jaundice after palliative operations in cancer of the ampullar zone MArurgiia no.3s8Z-86 163.. imin .1625) 1. Is kafedry obabobey khirurgii (zav,-doteant N.Merasimor) Saratovskogo meditsinskogo institutas Moms) (Bra Duas-waa) POPOWYAN, I.M., prof., otv. redJ' Oaratov); NAPALKOV, P.N., zasl. deyatell nauki prof., r4- ZAKHAROV, N.V., prof., red. (deceased]; BELISK ....-A.v-,#.,dots., red.; KOSHELEV, V.N., dots., red.; CIIAKOV3 L.G.; red.1 CIMNYSHEV, N.V., red.; BLINER, M.S., red.; ANDREYEV, P.P., red. (Transactions of the Second Congress of Surgenns of the R.S.F.S.R.j Trudy vtorogo s"ezda khirurgov RSFSR. Saratov, Vser. naucbn. med. ob-vo khirurgov., 1963. 583 P. (MIRA .17; 8) 1. Sllyezd khirurgov RSFSR. 2d, Saratov, 1962. BELISKrY, A.V. Furcate drain with two or three branches for hepatic ducts, removable in separate parts. Eksper. khir. i aneste noel 40-43163. (MIRA 16:10 1. Iz kafedry obahchey khirurgii (zav. - dotsent N.V. Gerasimov) Saratovskogo meditsinskogo institutae (BILE DUCTS.-SURGERY) (DRAINAGEl SURGICAL) BMISKIY dotsent (Saratov, Sovetskaya ul., d.31, kv.6) 1---.1 .1. .I Primary inflamma ory and cioatrioial narrowing of the hepatocyatic duat. Vest. Kbir. 91 no,1000-34 0 163, (MIR& 17&7) 1, Iz kafedry obahchey khirurgii (sav. kafedroy - dotsent N.V. Gerasimov) Saratovskogo meditainskogo inatituta (rektor - dotsent N.R. Ivanov). BELISEY, A.V., dotsent WPM Direct anastommila of two or three hepatio ducts with intestines having ~,-Icatriaial stru,,turaa, above their Junction. Sbor* nauch. rab. Sar. Cos-. mod. inst. 44-.246--251 164. almd-Lce in mali $ treatment bf pant t=ors of the porta he -)a tis. lbid.:251-256 OMM, 18; 7) 1. .1-, kafedry obshchey khimrgii (zav. dotsent N.V. GerasiTrov) J- Saratavskago lnsti,~uta (rektor dotsent lvanov). BELISKIY A-Ye-- KUYSLEVA, T.A. .I.avestigati-P4 the movement of mztor vehicles cn mountain --cads with prolonged upg--Mes. Avi. pron. 31 no.9118--19 S 165. (MIRA 18:9) lo Khabarovskiy pclitekhnichenkly Institulto BELISKIr,, A. Te. BELISKIYj A. Ye.s "Investigation of the movement of an automobile on the vertical curves of autombbile highways". Khar1kov, 1955. Min Higher Education U&M. Khar1kov Automobile and Road Inst. (DiBsertations for the degree of Candidate of Technical Sciences.) SOs KnizhLan LetoRis I No, 50 10 December 1955, Moscow. 5 E L2 S t;~ I ~' ~)- 1-1 e MOGIINTSKIY, Dmitrly Alsksandrovich, dotsentl BABKOV. Valeriy Fedorovich, prof.. doktor takhn.nauk-, SHMOV. Andrey Sergeyevich, kand.takhn. nauk; AMAKOV, Leonid Tikhonovich, kand.tekhn.nauk; ZA'YTSEV, Fi- lipp Takovlevich# kand.tekhn.nauk; ZAMAKEIATHV, Kitrofan Samenovioh. kand.takhn.nauk; NIKITINO Bergey Kikbaylavich, inxh*,* BIMIA, A.K., prof., retsenzent; DUDKIN, P.A., kand.tokhn.nauko reteensent; AVIMUT, V,N,g retsenzent; KARTASM, V.A.. retsenzent; PALICHEV, A.G., re- tsenzent; POPOV, A.N'b retsentent; PTITM. I.G.,.reteanxent-, ROKA- IMO, I.A., prof... retsenzent; BARATS, L.A., prepodavatell, re- teenzent; BlSMICH,,N9Iw, prepodavatall, retsenzent; BILISKIY, A.Ye., prepodavatell, retsefilent; MUZHMIY, Ya.A., prepod"ai;l ~.re~een- zente, CHYAROV, V.G.,'red.,; HALIKOVA, N.V.., takhn.red. 4ocating and designing airfleldej Isyskamlia i proaktirovaule sarodromov. Pod red. VJF.Babkovs. Koskya, Nauchno-takhn.isd-vo H-va avtomobillnogo transports i shoseeiuykh dorog R~M, 1959. 566 p. (MMA 13:3) 1. Kharlkovskiv avto'mobillno-doroshnyy Institut (for Romanenko, Barats, Baskevich, Bellskiy. Kalushaki - tT (Airporti-Planni j BELISKIT, A.Ye. I I Analytic calculation or motor-vehicle speeds taking into consideration the variable value of the coefficient of rolling resistance, Avt.orom. 29 no.10slO-13 0 163. (MM 16:10) 1. Frunzens*Kiy politekhnicheskiy institut. BEL'SKIY, P.B. 421+65. Kul'tura Kok-Bagly" V BSSR. Izvestiya Akad. Nauk. PSSR, No. 4v 1948, S. 71-76 DEWATY B.T3, BZLISKIY B.B* "The effect of'the koplication of mineral fertilizer on the yeild of kok-iagyz" Izventiya akad. Nauk DSSa, 1948 no 6, P 83-94 Idbliog: 8 items SO: U-3261 10 april 53,, (Letopis 'Zhurmal triykh Statey No U 1949) I I tT:VS`Yl S. 36325 Kulstura Kok-Sagyza Na Torf)ranykh Fbahvakh V Kolkhozakh Polesskoy Ob.".ftsti Izvestiya Akad,. Nauk Bssr, 1949, NO. 5, S. 119-28 SO; Letopist Zhutmalinykh Statey, No. /+9, 191+9 !~fj:skz. IsKy. Abod. %".M,:eSyz No 'rVO-10L.-Lituing tht oil Improves kok-%kl;hyi 1xi;t; in TCSPeCt to the d. of pL-mt growth atid in. =,Ilk wt. of wet or dry roots. Although the M- mlitagir of rubber latex Igopb, the yield per unit arm i, %ignifimlitly inirruzed. lk*t atilt. is oF l1k. hv,trolvtk- arwitv of the "I. G. It. KO-IIA;~Ufl BELISKIYj B. B.; . 6763. Bellskiy, B. B. , Kulakovskaya;.T.N. J Nyastyuk, N. N. I ~ Primeneniye udobreniy na torfyano-bolotnykh pochvakh nizinnogo tipa. Peredovoy opy-t. Minsk, Izd-vo Adad. nauk Belorus. SSR, 1954. 86 a. 20 sm. (Akad. nauk belorus. SSR. In-t melioratait', vodnogo i bolotnogo khozyaystva). 4.000 ekz. 1 r. 25 k. - Bibliogr: s. 84. -Na Belorus. yaz. - (55-2204) 631.615: 631.8 (47.60) & (016.3) ' SO: Knizhnaya Letopis' No. 6, 1955 9! BELISKIY, B.B. 475 SKOROPANOV,, S. G., PECHKURO,VA.IIF*i BII~KIY, B. B. Osusheniye i sellskokhozyaystuannoye osuoyeniye bolot v Belcrusaiio M. Se3!khozgis. 1954. 133 a. sill. 20sm. 5,.000 ekz. lr. 80k.-Na obl. avt. ne ukazanv.- L 54-544317 . 631.615(47-60)' SO: Knizhnaya Letopis, Vol. 1, 1955 % &V i Q11A 4B."kandidat sell skokho2yaystvannykh nauk.- IODNDYMVA, A.1h., -- 6W sotrudnik. Effect on crops of the type of underground drainage. Tray InBt. mel., vodA bol.khoz.AN BSSR 7;154-167 '56. (MI2A 10:5) (Drainage) (Oats) (Rya) BALISIIIY, Bronislav Bronislavovich - [Using fertilizers on bottom peat soils] Ushyvanne uhnsenniau na tarfiana-bolotnykh hlebakh nizinnaba typu; persdaV7 vooyt. Xinsk. Alcadleinia navyk Belaruskai SSR 1954. 83 p. WERA 10:9) (peat soils) ; (rartillsere and manures) USSR/Soil Science. Mineral Fertilizers. J-3 Abs Jour: Ref Zhur-Biol.j, No 6, 1958, 23742. B. Author Bel'skiy) B.; Kulakovskaya) T. Inst Title- Mobility of Phosphoric Acid In Peat-Bog Soil. Orig Pub: Vestsi AN BSSR, ser. biyal. n.) Izv. 0 BSSR) ser. biol. n.., 1956, No 2, 25-28. Abstract: Experiments were conducted in the Minsk Marsh Experimental Station on peat-bog soil in lysi- meters. Radioactive superphosphate was applied in the capacity of phosphorus fertilizer. The highest assimilation of the phosphoric acid by barley plants occurred with the application of fertilizers to a depth of 10 cm. Card 1/1 USSR/Soil Science. Tillage. Land Reclamtion. Erosion. J-5 Abs Jour: Ref Zhur-Dioi., No 6., 1958, 24836. was identical In distances of 5 and 10 m. between drains. The yield of oats on the lot with the clay drainage was hi(Shest at a 10 m. distance between drains. The lowest effectiveness of phosphorus-po- tassium fertilizers was registered on fields with clay drainage. The effective action of the slit drainage on the yield of agricultural crops is caused by the best conditions of aeration of soils. Card P/P USSR / Cultivated Plants. Grains. M-3 Abs Jour: Ref Zhur-Biol., 1958, No 16, 72920. Author : LLLqKiy2 B. B. I b Inst :Not given. Title :Fertilization of Corn on Peat-Marsh Soils. Orig Pub: V.3b.; Kukuruza v BSSR. Minsk, AN BSSR, 1957, 191- 200, Abstract: Experiments of the Institute of Amelioration were conducted at the Kossovskaya Experimental Marsh Station in 1955. The corn harvest, especially of the ears, and their ripening increase with the in- crease of P and K doses. With a dose of P30 KlOO of active substance the harvest of green ri;ass of the corn was innreased by 10.8 and of ears by 14.2% in comparison with the control (311.7 centnera/ha. of green mass and 87 cwt/ha. of ears). increase Card 1/3 USSR / Cultivated Plants. Grains. M-3 Abs Jour: Ref Zhur-Biol., 1956, No 16, 72920. Abstract: the seeds 2-4 cm away. Cu, Co and Mo applied in the soil before planting at 5 c/ha in the form of pyrite cinders or cobalt wastes increased the har- vest of green mass and ears. Soaking the corn seeds in weak solutions of microelementB provided an ad- ditional harvest of green mass by 20.5-24.7 and of ears by 15.6-29.5% in comparison with the control. M, A. Novoderzlikina. Card 3/3 SKOROPANOV, S.G., glavnyy red.; PECHKUROT, A.F., kand.sellokokhoz.nauk, red*; KHOTIKO,,A.I., kand.sel'skokhoz.nauk, red.; IVITSKIT, AvIs, doktor takhn.naukq red.,; MISKITO B.B., k9nd.sel'skokhos. nauk, red.; MARIKS, L., rad.izd-va; VCLOEI"OVICH. I., takhn.red. EAchiavements of the science of land reclamation in the White Russian S.S.R.; works of the institute dedicated to the 40th anniversary of the White Russian S.S.R.) Dostizhenlia malio- rativnoi nauki v BSSR; Lastitut k 40-latiiu BSSR. Minsk, Akad. nauk BSSR, 1958. 193 p. (MIRA 13:6) 1. Minsk, Beraruski naukova-dasledchy instytut meliiaratayl i vodnoi haspadarki. 2. Chlen-korreapondent AN BSSR (for Skoro- panov). (White Hassia-Peat soils) ZUBETS9 V.M., red.; SECROPANOT, SoG., red.;IBMISKIT, B.B.. red.; LASURY CH, G.I., red.; KHOTIKO, A.-I., red.; SA OTA, A* o. red.; 13MMMOT, T*M., tekhred. (Cultivation practices for groving field crops on peat-bog soils] Agrotekhaichaskie trebovanlia po, vozdolyvanliu seliskokhosiaistyennykh kulltur no torfiano-bolotnykh pochvakh. Minsk, Izd-vo Akad.sellklios. nauk BSSR. 1960. 79 p. (mmA 14:1) 1. Minsk. Havukova-dealledchy inetytut meliarateyi i vodnal haspa- darki. (Field crops) (Peat soils) SKORCFANOV, B.G., glavnyy red.; PECHOROV, A.F., kand.sellskokhoz.nauk, red.; KHOTIKO, A.I., starshiy nauchnyy sotrudnik; red.; ITITSKIT, A.I., doktor takhn.nauk, red.; ~and.sellskokhoz.nauk, red.; FROKOFXNKO, D.P., tekhn.red. [Principal results of research carried out by the White Russian Scientific Research Institute of Land Reclamation and Water Management in 19571 Oanovnye resul'taty nauchno-issladovatellskoi raboty institute za 1957 god. Minsk, 1958. 280 p. (HIRA 14:2) 1. Minsk, Belaruski navukova-dasladchy instytut maliaratayi vodnai haspadarki. 2. Chlon-korrespondant AN BSSR (for Skoropanov). (White Russia--Drainage research) (White Russia--Agricultural research) BELISKIY, B.B.; KULAKOVSWA, T.N.; ROZINA, M.S. Determining phosphate availability in peat-bog soils. Pochvovedenie no.11:93-98 N 161. (MIRA 14;12) 1. Belorusskiy nauchno-isslei*vatellskiy institut melioratsii i vodnogo khozyaystva. (Peat soils) (Soild--Phosphorus content) ZUBETS, V.M., otv. red.; LASIIKEVICH, G.L., red.; PECHKUROV, A.F., red.; IVITSKIY, A.I., red.; BELISKI'Y'a' B.B., red.; LUNDIN, K.P., red.; IAISHANOVA, Ye.A., red.; ThfitHCHUK, R.S.3, tekhn. red. [Draining and utilizing peat-bog soils) Osushenie i ispoll- zovanie torfiano-bolotnykh pochv. Minsk, Gos.izd-vo sell- khoz.lit-ry BSSR, 1963. 316 p. NLRA 16-.12) (Peat soils) (Drainage) BELISMY, Bvonislav Brcnislavcvi,:h;, Ye-~,- I.A. [P.Ole of chemistry In the efficient utilization of peat- bog soils] Roll khimii v effektivnom ispoltzovanil tor- fiano-bolotryykh pochv. Elnsko Izd-vo "Urozhai," 1.9b4. 36 p. WdiL't '117 :"?;, DEL: stf tY, 13. E- . I N"i" - SeJL ( L-C_ BRLISKIY, B.I. Collophane blinds (FLIMS) against flies. Gig. i san. 21 no.11:96 N 156. (WINDOWS) (MMA 10:2) meow, Portable trap for synanthropic flies and blood-sucking insects [with eumwy inIngliable Medeparax. I, paraz.bol, 26 no.2:222-225 .Nr-4P '57. (MLRA 10:7) 1. Iz Rovenskoy oblastuov sanitarno-spidemiologichaskoy stantaii (glavuyy vrach L.Y.Bulanov) (PLISS portable fly trap) AUTHOR: Rel'skiy, R.T., Candidate of Agricultural ')cience 26-58-6-54/56 TITLE: Mass Transmigration of Caddis Plies (Massoviye perelety rucheynikov) PERIODICAL: Priroda, 1958, Nr 6, p 127 (USSR) ABSTRACT: The author reports two incidents where caddis flies migrated in large numbers during daytime. The flights were apparently caused by heavy clouds and strong winds. The swarms varied between 200-1100 m in length and were rushing along with the Card 1/1 wind at 10 to ICO m altitude. ASSOCY-MM Oblastnaya sanitar.Wa epidemloloWichesk7m stantaiyaga Rovno (Oblwt Sanitari-m Epldw--olloglcal Stet-_!On, c:Lty of Rovno) 1. Fl-ies-'Kigration SAVVA) David Abramovich; VLASOV) Nikolay DmitriyevichIBELISMY B.R. spets. red.; SHEMTTO, Ye.P., red.; ZAYTSEVA,-L-.X., ~.-;red, (Using the production-line method for vatch and clock repdrel Remont chasov potochno-operatsiowWm metodom. Vloskva, Gas.izd-vo mestnoi. promyshl. i kbudozh.promyslov, IWSR, 1961. 133 P. (MIRA W-12) (Clodke and vatches.-Repairing and adjusting) (Assembly-line methods) KOROBOCHKIN, I.V., kand. tekhn. nauk; _B&L'SKIYA B,.&, 14. ; MIKHAYLOV, Ye.A., inzh.; GUTENMAKHER,. L.I.,, laureat Stalins4 premii doktor tekhn. nauk, nauchnyy red.; SEVOSTIYANOVA,'M.V., doktor fiz.-mat. nauk, prof., nsuohnyy red.; RUSEVICH, I.M., lnzh., red.; OSTROVSKAYA, Ye.G., otv. za vypusk [Catalog-manual of laboratory'devices and equipment] Katalog- spravochnik laboratornvkh priborov i oborudovaniia. Moskva, Masbgiz.,No.21.[Calculating machines and~Aevices] Schatno- vychislitalinye priboryi apparaty. 1948. 22 p. Wo*27. (Micro- scopes and lensea] Mikroskopy i lupy. 1950. .87 p. (MIRA -16:4) 1. Moscow. Vseaoyusnava vyatavka otecheBtvennogo priboroatroyeniya, 1948. (Calculating machines-Catalop) (Microscopes-Catalog3) (Lenses-Cataloge) BELISKIY, D.D. Measurement errors ol dial and lever-type indicators with racks. Izm.tekh. no.7:60 J3. 162. (MIRA 15:6) (Recording instruments-Testing) OMELICHEM, P.; IMLISKIT9 I* -W-4 We are repairing our dredge. lolyms 21 no,2:8 7 159. (MIRA 12:7) 1 ~Irags No.173 pritska im. Gastello (for Omellchenko). 2*"Draga i0*174 priisks, N .3.74 (for Bellskir). (Kedging machinery-Maintenance and repair) BELISKI7, G.M. (Sweromorsk) I Darmographism in axudative pleurisy. Klin.medo 38 no.10t41- 420 160. (MnA 13 t3.1) (DEMOGRAPB3A) .(PLWJSI) BELISKIY., G#Pq, podpolkovnik Important condition for the care of material, Veat.protivovoide obor. no.9-.61-63 S 161. (MM 14:8) (Commmications, Yd1itary-11hintenance and repair) , BELISKIY. G.V.z SHAV10, S.G. Some regularities in the distribution of metallic elements in rocks of the central Ralba. Uzb.geol.zhur. no.5:/+3-49 161. 1, Institut, geologli AN Uzbekskoy SSR. (Kalba Itang&-Metals) BELISKIY, G.V. *thods of-sVdyiag the distribution of metal elements in rocks as revealed by the studies in the Altai. Trudy AltGMII AN Kazakh.SSR 12:70-75 162. (KMA 15;8) (Altai, Wuntains-Rocks-Awaysis) A~kl, 4BUDARIU, P.M., red.ixd-va; TWIN&, Te.L., tekhn.redo (Stability of compressed steel rods witb flexible fixed ends] Ustolobivost' ashatykb utallmykh stersbnei a uprugimi sasbehem- Inniiami kontsov. Moskva, 1959# 144 po (Mmdemila etroltel'stva i arhitAtury BEBR. lustitut stroltellnykh konstruktaii. Hauchnoe soobahchenie A0.10) (HIRL 13:3) (Blaatic rods and vires) BIMI SXIT G,Te Gommission on Metal Construction Xlemente of the Ccuuctl of Coordination. Ixv, ASU no. 3:133 160a (KIRA 13:12) 1. Voheqy sakretarl Koxissit po metallokonstruktsiyan Sovota po koordinatsit Almdemit atroitellistm t arkhitektury SSSR* I (Ilectrio lines--Poles) GEMWRLING, A.V., doktor tekhn.nauk; MIL%LY_ _G.Ye., kand.t.ekhn.nauk Bearing capacity of frames under elastoplastic conditions. Trudy TSNIISK no.7:33-62 '61. (NIRA 15:3) (Structural frames-Testing) BELISKIY~ Me., kand.tekhn.nauk TheoretDc'al and experimental investigations of the deformability and stability of elastically clamped rods. Trudy TSNIISK no.71 125-185 161. (MM 15:3) (Elastic rods and wires) IN MW 111 1 1111111 BELISKIY,.G.Ye., kand.tekhn.nauk Stability of centrally compressed rods and frames under elasto- plastic conditions. Trudy TSNIISK no.7t239-267 t6l. (MA 15:3) (Elastic rods and wires) (Structural frames) BELISKIY, G. Ye. Cand Tech Sci -- "Strength of rods and frames withib Qoe ralWe and beyond the now" of elastic deformations*" Mos, 1961 (Min of Railways USSR. Mos Order of Lenin and Order of Labor Red Banner Inst of Engineers of Railrond Transport im I. V. Stalin "MIT"). (KL, 4-61, 194) 143- 1 -2w- %. BELfSKIYJ G.Ye.1 DIGNISIADI, L.K. Inveatigation of mechanical properties of high-strength steels, Prom. stroi. 43 no.9t4O-44 165. (MIRA 18t9) BU SKIY I The-machines came. Mest.propoi khud. promys. 3 no.1:29 Ja 163. (HUI 16:2) 1. Direktor Kiyevo-Svyatoahinakogo zavoda khimicheskikh izdqliy. (Kiev-Chemical industry-Squipment and supplies) EELISKIY, I.F.; SHUYKIN, N.I.; GRUSHKO, I.Ye.; SHOSTAKOVSKIY, V.M. Interaction between esters of (3-tetrahydrofurylpropionic acid andits 0(-alkyl-substituted derivatives and phosphorus tribromide. Izv. AN SSSR. Ser. khim. no.9;1670-1671 165. (MIRA 18:9) 1. Institut organicheskoy khimii im. N.D. Zelinskogo AN SSSR. /-?z- Z- , ~ -k,/r / F/7-7- SHUYKIU,N.I.; TULUPOV,V.A.; BELISKIY,I.Y. ~ On the hydration of the furan ring. Zhur.ob.Wm.25 no.6:1175- 1178 Je'55- (MIRA 8:12) 1. Moskovskiy Gosudarstvennyy universitat - (Furau) (Hydration) SHUYKIN, N.I.; IML r - 10-09 1 Disclosure of the tatroliydrofuran cycle vith alumiz= halides. Tzv.AN SSSR,Otd.khim.x&uk m9.6:747-748 JTe 156. (Km 919) I.Institut orgamichaskey khimii imexti N.D.Zelinsk*ge AksAamii itauk SSM. (Awan) (Alwimum halides) ..~~L ~ I 1= Category: USSR B-9 Abs Jour: Zh--Kh, No 3, 1 957, 7592 Author : Shiykin, N. I., Grushko, 1. Ye. , and Bel'skiy, 1. F. Inst : Academy of Sciences USSR Title : On the Utilization of a Nickel Catalyst in the K zhner Decompo- sition of Hydrazones. Orig Pub: Izv. AN SSSR, Section on Chemical Sciences, 1956, No 5, 622-6Z4 Abstract The catalytic decomposition of the hydrazones of cyclohexenyl- cyclohexanone and o< -acetylfuran in the presence of platinized alumina (20% Pt), reduced nickel-alumina catalyst (3076M), or Ni-mud has been investigated. It was found that finely dispersed Ni-catalysts give product yields which are not lower than those obtained with platinum catalysts. Card ill -44- Ti -J" IM S, 50A K 'C.A 51 0-- j f,un 2-un, 64- V", - " , ~j--Ouz, T.NX'. ~ mud SOC~it sli,-,rwaW "I 7 vi, BEL I SKIYZ9 I, F, Cand ChemaSoL, ('diBs) "Cata-lytic: NIFAMSEW93:10 H~dro 13nolysis of tht-iibumt, 2n.� 9 MoS919-571. 10 pp 22 =4 (Academy o~saiences USSIV, Inst of Org=ic Chemistry im N". D. ZeUnskly), 1130 copies (XL, 25-5719 109)) - lg)- Catalytic Hydrogenolysia of Furan Compounds 79-2-27/58 reason for that should be sought in the shielding effect of the side group on the neighboring C-0 and C-C bonds. The by4rogenolysia reaction of furan homologues is raccamended as a method for the obtaiment of* certain less accessible alkyl alcohols and ketones. There am 19 references ofvhich 9 are Slavid ASSOCIATION: USSR Academy of Sciences, Institute of Organic Chemistr7 PRESENTED BYr SUMUTTED: March 24j, 1956 AVAILAZZ: Library of Congress Card 2/2 On the Interaction of Tetrahydrofuran with Silicon Tetraohlorid. robutanol as well as sicilic ae id. The correctness of the assu- med structure is confirmed by the fact that the entire quantity of tatrahydrofuran and approximately half the quantity of the silioon-tatr&ohloride enters into the reaotion if it is carried out by equimolar quantitLes of these substances. Thau 1.4-dich- lorobutane and Di (0'0'-olorobutoxy)-dichlorosilane develop from this as the main products. Furthermore, the carrying out of the reaction is described in detail. The reaction under consideration can serve as a method for pro- duoing oxygen-containing silico-organic and clorino-substitutod aliphatic alcohols. (With 9 citations from publications). ASSOCIATION Institute for Organic Chemistry "N.D.Zolinsky" of the Academy PRESENTED BY SUBMITTED 27-10-1956 AVAILABLE Library of Congress Card 2/2 20-2-37/67 AUTHOR SHUYKINJ N.I. Corresponding Member of the Academy I and JEL SKIY I TITLE - The ~a ~aiyl~icHjydrcgenolysis of Sylvan on varied Catalysts. (Katalitiohoskiy gidrogenoliz silivana na, razlichn7kh katalizatorakh.- Russian) PERIODICAL Doklady 1kademii Nauk SSSR 1957v Vol 1159 Ir 29 pp 330-332 (U.S.S.R.) LBSTRACT The hydrogenolysin reaction of furan homologs depends on.-three factors, namely an the operating conditions, ,the nature of the catalyst and on temperature. In the sylvan hydration in the liquid phase An copper chromite the furan cycle is split to almost the same extent on the ether'bondx 1 - 2 and 1 - 5. As a result develop pentanol-I and -2, In oontzasit to that the sylvan hydro- genolysis in the liquid phase on the Adams platinum catalyst occur& only in the direction of a splitting of the C-4 bond 1-5. The same in true for the hydrogi- nolysis in the gas phase on nickel and copper catalysts, however there dOT010PS no alcohol but a ketone (pentanone-2). In earlier work* t4authors studied the same reaction of furan homol~es In the gas phase CARD 1/4 2M~-37/6T The Cata4tic Aydroffenolysis of Sylvan on Varied catalysts. on a skeleton niokol-aluzibAum catalyst and proved that thereupon takes place a hydrogenolyBis not only of the other-, but also of the carbon-carbon bonds in the f-mran cycle. Ill furan homologs with an alkyl- or alkenyl substituent in an a-position are subject to hydrogenoly- sis in three directions. k eohema for this Is given. At I75*C and below the furan oyale undergoes a hydra- genolys'is only in directions I and II (of the scheme), above 23500 also in direction III. The present paper ,gives test results of the sylvan hydrogenclysis in the fa;%5hase in thelvesenae of various oatalysta: platinum I an,1 palladium (10~) on charcoal, Adkins copper chromitep nickel (30 ~0 on alumijaiumoxide an& skeleton nickel-aluxinium catalyst. The re3ults of this study lead to the conclusion that the direction and depth of the hydrogenolysis of the furan cycle esjqenfikly depends on the nature of the catalyst. Platinum on- charcoal possesses the seleotive ability to cgrry out the hydrogenclyals of the cycle in sylvan only on the other bond I - 5. The presence In the remotion products only of pentanone-2 and unchanged sylvan shows that, at 2T50C the hydrogenolysis reaction on the platinum CARD 2/4 catalyst occurs iscomparably faster than the hydrogens- 20-2-37/67 The Catalytic Xydrogenolysis of Sylvan on Varied Catalysts. tion of the double bonds in the cycle. Pentanone-2 practically forms with a quantitative yield In rela- tion to the sylvan that entered the reaction,. In contrast to that the palladium catalyst proves much more effective in the hydration of double bonds of the cycle and shows only insignificant activity in the hydrogenolysis of the ether bond. Just as on pla- tinum, the furan cycle in the presence of a palladium catalyst is subject to hydrogenolycis only on the C--O bond 1--51 whereby pentanonc-2 deyelope. Copper- chromium catalyst shows a rather weSk activity in the hydration and hydrogenolysis at 275 C. In contrast to the bydrogenolysis on copperchromite in the liquid phase which leads to the formation of two alcoholop the reaction here in the gas phase takes place dtly in the direction of a splitting of the other bond which does,not border the side group. The mentioned skeleton catalyst and nickel on aluminumoxyde differ CARD 3/4 widely with regard to their ability to carry out the 20-2-37/67 GARD 4/4 The Catalytic Hydrogenolysis of Sylvan on Varied catalysts. hydrogenolysis of the furan oycle. On the latter about 15 % ketones form at 275001 85 % of the ostalyeate consist of unchanged sylvan, n-pentane and high-boiling compounds. This indicates that the prooeases of faxrasrXw, ing decomposition of the furan ring and the formation of molecules of complex composition is favored by tbis catalyst. On the skeleton nickel aluminium catalyst the hydrogenolysis takes place in three directions. These results are in agreement with those obtained earlier. Thus only the skeleton catalyst is able to carry out the reaction as well in the direction of splitting the other bond 1-5, as of a conjugate aplit- ting.of the linkages 1-5 and 4-59 and of 1-5 and 3-4- This permits to obtain aliphatic ketones of various structure from alkyl furans. (3 Slavic-references) ASSOCIATION: Institute for organic chemistryim.N.D.Ze1in9ki* of the Academy of Scienoesof the USSR. (Institut organiaheskoy khimii in. N.D. Zelinskogo, Akademii nauk SSSR) PRESENTED BY: SUBMITTED: 27-3-57 IVAILABLE: Library of Congress. F AUTHORSt Shuykin 9 N. I Correspooling Member of the 2o-4-26/~i AN SSSR and -'ITLE: The Hydrogenolysis of Furane Homologues on a Platinum Catalyst (Gidrogenoliz gomologov furans, na platinovom katalizatore) PERIODICAL: Doklady AN SSSR, 1957t Vol- 116, Nr 4, pp. 621-624 (USSR) ABSTRACT: After an exhaustive review of references the authors make the comprising statement that the hydrogenolysis of the furane cycle in a general case depends on the nature of the catalyser, further- more on the character of the lateral substituent, on the tem- perature and on thetphase (Liquid and vaporous) in which the re7 action takes place. The auV-.ors investigated the reaction of the a-substituted furane homologues in the vapour phase on 15% platinum, deposited on activated Virch coal. The length of the lateral chain of the furane homologues was chosen from C1 up to C5 in orderto be able to evaluate the influence of the chain length ofthe alkyl lateral group on the character of the hydro- genolysis. It was found that the furane cycle under these condi- tions at 2750, independently of the chain length, splitted at the C-LO-binding 1-5 which is not adjacent to the lateral group.. Here aliphatic ketones are formed with yields of 9o-95,P"' of the theoretically possible.yield. At this temperature (2750) no al- kyl tetrahydro-furanes were found. However, at 2300 from the hy- Card 1/2 drated a-n-propyl furane beside heptanon -4 also a-npropyl-tetra- The Hydrogenolysis of Furane Homologues on a Platinam Catalyst. 2o-4--26/51 hydro-furane was obtained in a quantity of 16,,;.' of the catalyst weight. Thus the lower temperature favors the re4ction of the hydrogenization of the double bindings in the furane cycle, whereas an increased temperature is favorable for the hydro- genolysis of the other binding 1-5. In the experimental part the usual data are given. Final oonolusions: It was found that in the case of hydration of the a-alkyl furanes in the vapor phase on platinized coal a elective hydrogenolysis of the furane cycle on the C-0-binding 1-5 taken plaoc, a fact by which aliphatic ketones with high yields are formed. There are 2 tables, and 8 references, 1 of which is Slavic. ASSOCIATION; Institute for Organic Chemistry imeni N. D. Zelinskiy AN USSR (Institut organicheskoy khimii im. N. D. Zelinskogo Akademii Nauk SSSR) SUBMITTED: July 10, 1957 AVAILABLE. Library of Congress Card 2/2 20-5-24/48 'AUTHORS t Shuykin, N. I., Corresponding Member AN USSR, Bellskiy, I. F. and Tyant Sin-Khua TITLEt Hydrogenolysis of o6 :.Methyl-d_'-Ethylfuran on Platinized C~_farcoal (Gidrogenoliz 0~ etil-061-etilfurana na platinirovannom ugle) PERIODICALs Doklady AN SSSRj 1957, Vol. 116, Nr 5, PP- 608 - 810 (USSR) ABSTRACTs For the purpose of comparison the authors investigated the hydro- genolysis of silvan at various catalysts. The furan ring in silvan can be splitted at a platinum-, pa;ladium~v and copper-chroaium catalyst in the vapor phase at 275 at an ether binding not ad- joining to a lateral group. This leads to the formation of me thyl- propylketone. Only the platinum catalyst shows the power of split- ting the furan ring selectively at the C--O- binding without any secondary processes. In contrast to all these catalysts the skele- ton-Ni-Al-catalyst has specific powers to carry out the hydrogeno- lysis of the furan ring in the direction of cracking of the ether binding 1 - 5 as well as I - 5 and 3 - 4- In the last case ketones are produced which contain in the molecule 1 or 2 carbon atoms less than the initial alkylfuran had. This is to be called the Card 1/3 "conjugated" hydrogenolysis. In all cases the influence of the la- 20-5-24/48 Hydrogenolysis of o(--JUethyl-ot'-Ethy1furan on Platinized Charcoa ,1 teral-alkyl-8ubstituent effects an almost complete incapability of the C-0-binding I - 2 of hydrogenolysis. Therefore it was inter- eating to investigate the comparing capability of the C-0-binding of the hydrogenolysis which are influenced by 2 alkyl groups with different lengths of the cai:bm chain. If the reaction at the ether bindings I - 2 or I - 5 mentioned ir4the title is carried out, hep- tanon-3 and heptanon-2 are bound to be 8roduced correspondingly. The first substance was obtained at 235 in the vapor phase with a yield of 54 %, the latter with 36 ~S. N-heptan (ev7lo) was present in a con3iderabld smaller quantity. Its fornation is effected by a simultaneous hydro-enolysis of the furan ring at the C-0-bindings 1 - 2 and 1 - 5. The relative content of the two first ketones in the products of the hydro.-anolysis leads to the conclusion that the ethyl group exercises a much more stabilizing influence on the adjoining C-formation than the methyl group. Theexperimental part with the usual data follows. There are 3 references, 2 of which are Slavic. Card 2/3 Y." AUTHORS: Shuykin, ff. I., Corresponding Member of the 20-1-25/42 AN USSR and Bel'skiy, I. F. TITLE: Note on the Selective Reduction of Alkyl-Furyl-Carbinoles to Alkylfuranes on a Palladium Catalyser (Selektivnoye vosstanovleniye alkilfurilkarbinolov v alkilfurany na palladiyevom katalizatore). PERIODICAL: Doklady AN SSSR,'1957, Vol. 117, Nr 1$ PP- 95-97 (USSR) ABSTRACT: The hydration reaction of compounds of the type CH-R f where R may denote a hydrogen atom, UO I OH a alkyl or an aryl radical, has been throughly investigated with respect to the multiplicity of compounds as well as to the number of the catalysers employed. According to the nature of the last and according to the structure of the compounds the hydration may take three directions: Card 1/4 1) The double compounds of the furane cycle are the only Note on the Selective Reduction of Alkyl-Furyl-Carbinoles 20-1-25/42 to Alkylfuranes on a Palladium Catalyser ones that'are hydratedo in such a way as to produce alcohols of the tetrahydrofurance series. 2) The hydrolysis of the cycle takes place at one or at both C-0 bindings, wherefrom "alkandioles" and alkanoles are produced. 3) The lateral group may be reduced entirely, the hydroxyl being replaced by a hydrogen atom. Pinally, all or some of the abovementioned reactions can take place at the same time under certain conditions. A comparison is Given between the nickel- platinum- and copper catalysers employed for these purpooes. As it Is well known, palladium represents an excellent catalyser of the double bindings of the furane cycle in the 'liquid as well as in the vapour phase. The attempt of the authors to hydrate the furane ring of the compounds mentioned in the title at palladisated coal lead to surprising results: Instead of a hydration of the double bindings in the furane cycle a hydrolysis of the C - OH bindinre and the replacement of the hydroxyl group by a hydrogen atom took place. This lead to a conversion of the Card 2/4 ethyl- and methyl-furyl carbinole3 to the coxmsponding Note on the Selective Reduction of klkyl-Paryl-Carbinoles 20-1-25/42 to ilkylfuranes on a Palladium Catalyser a-propyl and a-ethyl furanes, yielding 70-80 % of the theoretically possible production. This ability to split forms a specific property of this type of compounds. It does not occur in pentanole 2 at much higher temperatures. It is a remarkable fact, that the hydroxyl group of the alkyl tetrahydrofurylcarbinoles is not even capable of reduction. Therefore the C - 0 binding is weakened only in. alkylfurylearbinoles to such an extent, that it in easily broken up by hydrogen on palla disated coal. The reason for this may be sought in the fact, that the 0 - 0 binding in the lateral chain is conjugated with the double binding of the furane cycle, Methods of production for the initial substances are given. The reaction of the reducing des- hydroxylisation of the alkylfurylcarbinoles into alkylfurane constitutes a very interesting instance of the selective effect of the palladium catalyser. kpart from its theoretical interest it may be of great importance in a preparative respect, for it provides for an avoidance of the stage of the dehydration of the alkylfurylcarbinoles in the synthesis of the alkylfuranes, which, in general, does not roceed Card 3/4 smoothly.There are 8 references, 2 of vihich are Ofavic. Note on the Selective Reduction of Alkyl-Furyl-Carbinolea 20-1-25/42 to Alky1furanes on a Palladium Catalyser ASSOCIATION: Institute for Organic Chemistry imeni N. D. Zelinakiy AN USSR (Institut organicheskoy khimii im. N. D. Zelinskogo Akademii nauk SSSR) SUBMITTED: July 10, 1957 AVAILABLE: Library of Congress Card 4/4 F AUTHORS: Shuykin, N. I., Bel'skiy, I. F.V 62-2-21/28 TITLE: The Catalytic Reduction of Alkylfurylcarbinols to Alkylfuranes. (Kataliticheskoye vosstanovleniye alkilfurilkarbinolov v al- kilfurany) PERIODICAL: Izvestiya AN SSSR OtdelerJye Khimicheskikh Nauk, 1958, Nr 2, pp. 240-240 (USSR) ABSTRACT: During the investigation of the hydrogenation of ethyl- and ethylfuryl-carbinols the authors discovered the interesting fact of the selective reduction of the above-mentioned com- pounds to a-ethyl- and a-propyl-furnaces. It was further found that the capability of the hydroxyl-group, to substitute in hy- drogen under the catalytic influence of palladium coal depends on the presence of the alkylfurylcarbinol cycle. In the reduc- tion of isopropyl- and butylfurylearbinols a-isobutyl- and a- -imylfuranes with a yield up to 7o~b' are produced. The experi- ment was performed in the vapor phase at 250-26o0. There are 2 Slavic references. Card 1/2 The Catalytic Reduction of Alkylfurylearbinole to Alkylfuranes 62-2-21/28 ASSOCIATION: Institute for Organic Chemistry imeni N.D. Zelinskiy AN SSSR (Institut organicheakoy khimii im. N.D. Zelinskogo Akademii nauk SSSR) SUBMITTEDs September 27, 1957 AVAILABLE: Library of Congress 1, A11qlfurylcarbinalB to allqlfuranes-Catalysis 2. Alkylfur7l- carbinals-Reduction 3. Allqlfuranes-Production 4. Palladium coal catalyst-Applications Card 2/2 62-58-3-9130 AUTHORSi Shuyking N. I. Bel'skiy, I. F. TITLEt The Catalytic Hydrogenolysis of Furan Compounds (Kataliti- cheskiy gidrogenoliz furanovykh soyedineniy) PERIODICAM Izvestiya Akademii Nauk BBBROtdeled~e Khimicheskikh flauk, 1958, Nr 39 pp. 309 - 315 (USSR) ABSTRACTs With the example of the preceding experiments the authors this time performed the lWdrogenation of the mixtures of some cA-alkyl- and ol--alkenyl-furans at 2350C. It was assumed that at this temperature an absolute splitting of the furan cycle must take place. Then products of the hydrogenolysis should form. This assumption was confirmed by the experiments. Moreover a new result of theoretical as well as practical importance was attainedt It became evident that the C-C-bond 3-4 readilg splits up at 235 0, but that at a lower tempera- ture (175 G) a hydrogenolysis of this bond does not occur. In this experiment the hydrogenation of 0the mixture of oC-n.butyl- and o(,butenyl-furanee (235 C) was performed in Card 1/2 a flow-system under ordinary pressure. In the presence of the 62-58-3-9/30 The Catalytic Hydrogenolysis of Furan Compounds skeleton nickel catalysts a complete splitting of the furan- -cycle in these compounds takes place. It was further found that the furan-cycle in these compounds is subjected to hydrogenolysie in the direction of the split of the C-0 bond 1-5) as well as in the direction of the split of the bond 1-5 and 4-5 as well as 1-5 and 3-470 It was found that the relative stability of the different bonds in the cycle of ot-n.butyl- and oe--n.amyl-furans depends on the length of the side chain. The authors obtained some data according to which the mechanism of the radicals of the hydragenolysis reaction of the furan-cycle can be assumed. There are 3 re- ferences, 3 of which are Soviet. ASSOCIATIONs Institut organicheskoy khimii im. N. D. Zelinskogo Akademii nauk SSSR (Institute for Organic Chemistry imeni N. D. Zelinskiy 7AS USSR) SUBMITTEDs October 27, 1956 Card 2/2 AUT11011S Shuykin, 21. 1., Bel Iskiy, I. F. 62-58-4-22/32 TITLE: Hydration of Alkyl a-Furylcarbinols on Ni-ZnO-Catalysts (Gidrirovaniye alkil a-furilkarbinolov na Ni-ZnO-kata- lizatore) PERIODICAL: Izvestiya Akade-,aii Nauk SSSROtdeleniyeKhimicheskikh ITauk, 1958, Nr At, PP. 506-507 (USSR) ABSTRACT: The hydration of alkylfurylcarbinols can take place in various directions accordine to the nature of the cata= lyst and the conditions of reaction. Lately the authors found (Reference 3) that the primary reaction in the hydration of alkylfurylcarbinols is not an hydration of binary bindinGa within the cycle but a reduction of the hydroxyl (.-group which leads to the formation of u-al= kylfurans. In +he present paper the authors report on the investigated hydration of alkylfurylcarbinols in gas phase on a Ni-ZnO-catalyst. In this they found that this catalyst (like paladini2ed. charcoal) effects as primary reaction the reduction of the hydroxjl Group in alkyl= Card 1/2 furylearbinols without touching the divisible bindings U 0 Hydration of Alkyl a-Furylearbinols on Ni-Z"JnO- 62-56-4-22132 -Catalysts in the furan cycle. There are 1 table and 3 references, I of wlich is Soviet. ASSOCIATION: Institut organicheskoy khiuii ita. If. D. Zelin3%oCo Alcaderiii naulc SSSR (Institute for Or-anic Chcmistry imeni 11. D. ZelinskiyIAS USSR) SUBMITTED: November 13, 1957 AVAILABLE: Library of Con-ress w lo Alky1furylearbinols-41ydration 2. R-UG-Catalysta -Xppl-teations Card 2/2 /S7A- Catalytic deh7dration of tetrahydrofuran homologues. Dokl. AN Azerb. SSR 14 no-2:115-117 158,, (MIRA 11:4) l.Institut organichaskoy khimii. AN SSSR. (Furan) (Dehydration (Chemistry)) I SOV/ 20-12o-3-31/67 AUTHORS: 1~huykin, M. io, Corresponding Member, Academy of Sciences, USSR, Bellskiy, 1. F. TITLE: Isomeric Transformation of I-Oxides (Tetrahydrofuranes) of Aliphatic Carbonyl eompounds (Izomerizatsiya y-okisey (tetra- gidrofurunov) v alifaticheskiye karbonillnyye coyedineniya) PERIODMAL: Doklady Akademii nauk SSSR, 1958, Vol- 12o, Nr 3, pp. 548-551 (USSR) ABSTRACT: Several chemical transformations of alkylene-oxides are under the action of various agents connee 'ted with an easily Pro- ceed.ing cleavage of the a-oxide cycle. The reiction mention- ed in the title i;OaWong those well studied. It proceeds from a heating to 300- 0 or lower temperatures in the presence of catalysts. Asymmetdo a-oxides, which possess one or two alkyl-substituents at one single carbon atom of the cycle, by a cleavage of the cycle are isomerized preponderatingly at that binding, which links the oxygen atom to that carry- ing the substituent. This leads to the formation of aldehydes (Ref 1). No analogous reaction was knwon to take place with Card 1/3 the comDounds mentionea in the title. The catalysts, which SOV/ 2o-12o-3-31/67 Toomeric Transformation of y-Oxides (Tetrahydrofuranes) of Aliphatic Carboni! Compounds are most active in the isomerization of a-oxides, with hydro- furane and its analogs lead to a dehydration reaction. It yielda diene- and aromatic hydrocarbons, The authors perform- ed the transformation reantions of tetra~ydufurane and of Its a-substituents on pla-tinated coal in the vapor phase 0 at from 230-250 . They found that these substances under these conditions isomerize to aliphatic carbonyl compounds with a simuitaneous cracking of the cycle at the C-0 links. Conclusions: 1) The a-oxide ring (tetrah.,-drofurane ring) is capable of the last mentioned transformations, by which ali- phatic carbonyl compounds are formed. 2) If an alkyl radical (CH 3' Y5 t n-C3H 7) is present in arx U-DOSitio'n of the tetra- hyd.rofurane cycle, the isomerization of the I-oxide primarily NP to 90-951~f*) takes place with a cracking of the cycle at the C-0 link. This leads to the formation of corresponding aliphatic ketones. 3) The aldehydest which are produced in small amounts in the isomerization of tetrahydrofurane and of "-alkyltetrahydrofuranes, suffer a cleavage at the C-0 link 112 and are subject to a decarbonylation to the correspond- .ing paraffin hydrocarbons under the prevailing reaction condi- Card 2/3 tions.