SCIENTIFIC ABSTRACT ALIMOV, O. D. - ALIMOV, R. Z.

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BASOVj, I&G.; ZELINGER, F,F,; YUDIN, V.G. Trenching in frozen ground with earthautting machines and excavators, Stroie truboprov. 8 no.8:18-19 Ag 163- (MIRW 16-:11) 1. Toyiskiy politekhnicheskiy institut. ALIMOV, O.D.. doktor tekhn. nauk; BASOVp I.G., kand. tekhn. nailk Earth-cutting equipment mounted on the buee of ETU-353 excavators, Mkh. stroi. 20 no.9:24-26 S t63. OIIRA 16: 10) (Excavating machinery) k'" - ALIMOV 0 D.- BASOV.. 1. G.,; MALIKOV, D. H.; LISOVSKIY, E. I. L~~ Results of trials performed tT a test crew on the RUP-2 mal chute widener. Ugol'-38 no.4:41-43 Ap 163. (MIRA. 16%4) (Coal uLning machinery-Testing) USHAKOV, I.A.; IlIKIN, Yu.K.; ALUM, O.D.; -MALIKOV, D.N.; SUOMI, I.A.; NEYANIlff~-S-.D-. Way of' erecting supports in upraise shafts. Ugoll 38 no.12:53-54 16.1. - (MM 17:5) ALIMOV D.; DOZMAROVp V.Z. . __) _2__ Creation of a bore hoisting machine on the basis of the UP-3 machine. Ugoll 38 no.12157 163. (MIRA 17:5)e,-.'.. 0.' 1. Tomskiy politekhnicheskiy institut. 4~ ALIMOV) 01D., joktor Lekhn.riauk; SADAKOVP YU.P., Jnzh.; SWIDT, A.A., limb.; VIJDINY V.G., in--h. Cutting.-bar machine with a hydromechanical reducing gear for working frozen grounds. Stroi, i dor, mash. 9 no,12:4-5 D 164. (MIRA 18:3) Ail 1? "1*1', ~ !91~ i. .teldin . nauY earth-cutting machInes on ~i trenz-h-excavator tase. St-,3i. i dor. rwtsh. 10 no.6:1-3 Je 165. (M75A 18-.8) AIIJWVP O.D.; tI.III)VA, A.A.; DVORNIKOV# L.T# TnVpStlgating bole drillJmg conditlois with the use of nomograms. Fiz.-takh. probl.. razrab. pol. iskop, no.I.:81-84 165. (MRA 19: 1.) 1. In3titut gornogo dela Sibirakogo, )tdeleniya AN SSSR, Novosibirsk I Tomsk-ly politelchnichoskiy institut, Submitted April 155, 1965. .,, 1~ _ , ... .. ALIM D., -.oktor tekhn. nauk; BASOV, 1.G., kand. teklin. nauk; ~ft "UR 1. YETANNT, F.F.~ inzh. Experimental investigation of cutting conditions of frozen grounds with an. earth-digging machine. Stroi. d dor. mash. 10 no.9:1-4 S 165. (MIRA 18:10) , 71 , ~~,17 -I A- ) . . Certrarinial ~.f thf: Forestry Schr,~,!. Ler.-. 1-h-o?. ".-I I 1Q~I- .. ~ . p -1 '.4 . ~ f-, T) P SO: . 1-11.11 19,1~2 MALiTSXV. A.M.; ALIMOT P rodaktorl YMUIMRNKO, V.Ye., radaktor; ZAKIROY, K.L., akili-a-M-1'e, ft, 9r; XAWH. S.So, akademik, radaktor; KOROVIN, To.P,e almdsmi~. redaktor; MUKHAMKDZEANOV, M.V., alaidemik. redektor; NABIYBV, M.N., alcadamik, redaktor; RYZUOV,-P.N., radaktor; SADYKDV, S.S.. redaktor; ITZINBAYAV. Ye.1h., doktor sellakokhozyaystvennykh naxiko redaktor; KILIMAN, Z.A., redaktor Watellatirs; BAR&KHANOVA, A.G., talchnichaskiy redaktor [The cotton plant.) K~lopchatnik. Tashkent. Izd-vo Almdemi-L nauk Uzbekskol SSR. (Introductorv volume: The cotton plant and the use of its -fiber] Vvedenie: Xhlopchatnik i ispolPisovento volokna. 1956. 1213 p. (PI&I 10:3) 1. Tashlaint. Vessoyuznyy nauchno-isoledova tell skiy Institut khlopko- Yodstva. 2. Chlea-korrespondnet Akademil nauk UsSSR (for Alimov, Yeremeaka. Hall tsev, Sadykay, Kanash). 3. Vessoywinaya Ahademiya sell skokhozyaystva,nnjykh nauk Im. lenina (for Kanash). 4. Chlan- koresspondent Vass oyuznoyAksdemii sell skokhozyaystvannykli nauk im. Isnina (for Ry-zhov) Notton) USSR elldstry -,.'Organopho lipbortw Compounds' "Action of Strong Inorganic -Acids on Some Esters Of Phosphorus Acids," A. Ye. Arbuzov, P. I. Alimov, Cbim Inst imeni Acad A. Ye. Arbuzov, Kazan' Affiliate, Acad Sci USSR "Iz Ak Nauk SSSR, Otdel Kh1m Nauy.,;; No 3, pp 268-2'72- Sulfuric or phosphoric acid, similarly to HC1, splits triethylphosphite into diethylphosphorous acid and etbyl ester of the inorganic acid. Action of HU on tetreethyl pyrophosphite results in formation of 4ej;~yiphospaorous.,acid and diethylpbosphorous acid u S Th e Organopbosphorus May/jun r mis try compounds (Contd) chioride. iliction of HC1 on tetrae-~hyl bypophos- rj~z--~-te results e-ithe'r in formation of diethylphos- phoric actd- chloride (I) and diethylphosphorous, acid (II) or of. diethylphosphoric acid (III) and di~tl-iylphosphorous acid chloride (IV), Following' products of this reaction were isolated: II, IV, ..tra,eth-yl --nnhon-phatp IV). V ~,a prPrIlli't' -of.i secondarv reaction between I and III. 18 W-9 LC nis UWM/Chmigvtry - 'Orgisn4b~)spho Jul/iug 51, V Compounds CY "C6bined Anhydrides of Carboxylic. Acids'and Di- etbylphosphorous Aci4," A. Ye. A'rbuzov, P. I - Ali- mov, Chem Inat imeni. Mad A.. Ye. Arbuzov, Kazan' Affiliate,,Acad Sci USS9 "Iz Ak Nauk SSSR, Otdel Min Nsuk" No 4J, pp 4og-416 Action of isobutyric, butyric, isovaleric, cro- tonic, capronIc benzoic p-toluylic acids on (EtO)O-O-P(EtOj, yielded' combined anhydrides of type RCOOP(OM)2 prepd for the lot time, vhich 192T21 USSR/Chemistry - Organophosphorus Tul/Aug 51, Compounds (Contd) react in the manner of acid anhydrides. Under ac; tion of EtI, they form by Arbuzov reaction isomer contg P54 atom (phosphonic acid-carboxylic. acid .inhydrides) and high-boiling substances of undetd Structure. L1 Vic. V 1. h of "mileatimille oil "we of A. V. AvIsumv ".Ck I a - I .. R a I r a 10. - " -.4'" 0. A' N.V.'% OV, 44M. KAIto. Nook lost WIP-6 I" Isminali-M 44 4INWVI 4k#4wI. lesions ALIVhV%i;4 a ith.-allstrivi"' stallylkid". oldwhydc. "mi 04 Ilse I tylsc (HU16110CUMN IPxOmh. 111ant, heating 4 2. = If 14.1 "111041`1 0)(Ilinawakd lUbt I bf. M lilt' save 8.2 0. (Wh1VC/1.Wrmt)XOA2)1 (111), 111 1 lop-1111. ;V 1XV0. d:" IJPJI. stal. so two. matIvriml- mIA list), TOO." . I OW 1'73 It. IIICIIO was added 1 411%111 whull Overard a Irtup. liar lo.47', istsid allm III whs, at 101" the isdul. tom .1 1. 01~1114110[ 11114jokoh.01., 111 134 A". mV 1.43mi. d:' Ilculing 7.4 1. 1 with V.Th 0. IIIIIIIIal 410 utin. of IAP' I we mill"t 2 Ifistus. IA 2. ~Eff)41'001- jzur Ift.. ;140-141. atF 1.4116q, III, 1.114WI. wftb.'I.l g. hill I hr. .1 119," gave 4.7 c. W41110CUP111)"(0)(ONIth bi mT LOW, d:0 gave the #44~d mossApt. Is. 16111-4111". -V 1.4101. d!j' 1.1 IAIL tins .1cm odda. of 2A a. CW010 I- 7z It. I bent was rv%s1vv4 Ow w #V-. 1 .10.1 all't Ill Ini". .1 14110 W* rIr t~ 1ajnrd2,JSx. (mill" art tial dlAns.) (110 41%'1, 1 its 41 -3% tirul 3-Ji I- U-20.111%O)i t lot 1141, list W# it'. 0117 1.4410.1. 1111 -/0 Thelat. 'I %%Iih I %at .41-1 4-Imallml. a litim-1 III its stivollurr. in ~!II* .. a I's W. .4 7.4 6. 1104141, to a 6 g. 0'. VIII 1. ItAII-0 I-v In-aling III nun. at L111 411% thr im-ol, int It., M 7'. 111.* 1.11411. d.11 I,Zkll. No trist-fism It%* Itlare bet'siven 1111- IWWtk't Mill 1. 1 aho failed to resort uilh Mr.W. II lumled 6 his. with It% IICS, thm briedy mith 11640t, sg%r 04-14-% IIcCI. f4inflaily the (uto), IwIll-hiNowV1 4 (IIIj save 1111.411, 1110, In dialysis no thr 14PIl .1flit , I. III, At fl-1111% with '4111; 110, 1:41cmajA fly irlwalt'l r%alm. Willi 11.4). MJII. .4 Itar Irsid" In Hirst, And tims At-011-C411q, save PACII(Ollf- 1104011h, In. I - . 'j a , f%wifirl"ing Ike al"Irturv. fleating '1;t J.N.1 S. I %Sill I "jI'HI I IRA neatest lubc, 4 hn. at 140" gave A. (MJ`h1%())001rO1%OXOSlW, Is, 132-3-, of: 184"Imirly Ill in :11 his. Ail iji-M. save (FjOh11O)cj1pAO1xOxt)E#)- A.I. 111. 17-0-7% -1* lAtM. d.' 1.1624. in allismost. I(VI% vwkl. 11 reacts with (Cu.Xh with evolutints of beat. but llw it'Isluct. f-ul't n-01 tw It. 161. K. "L, Y phosi ior iva Ves'll Tu 4j~ ,M:~ AW W.' il.6 or, i ran pr .'j7 it, 'An. -i. aik -.prol im y1sm he ~Opp -th~.. elpeam deg.~ T dj,,'were-- price ly ft iivc66iate~ r ab,~i hol a act act 0 -0 no .t.dus'~,!or alII ~Preslahce_l 1 0 with, el ud 3, V2 L ~3 rt A(Ir P AP ACC OSSION r VovA, -1kadeki- ~~W ~4 tho g emy ~t " - I I SUBMITTEDt' F AIM ij, i~ ~F, 3111 1- ,A, 11 '14 111i, 0: ALIKOVs P- 1* ARBUZOV, A.Te.-, ALIMOV, P.I. ,!' Condemoation prod-acts of pyrophosphor-,ja acid esters with alaekvdes. Izv,.K&,ian.fil.AN SSSR Ser.liim.nauk no.1:21-30 150. (Fyrophouphorous acid) (Aldehydes) (MLRA 10:5) ARBUZOV, A.Ya.; AMMOV, P.1 If fact of strong irdneral acids on certain phosphorus &aid esters. Izv.Kazan,,fil.Ah SSSR Ser.)chim.nauk no-1:39-44 150. ktiLM lo*..-)) (Phosphorus acids) If A 6 h era d'As;A cA6~ o~ -;Y.Oddlis ahimals'', Mid e-, r nd: bSA (10~1 T Puib UZO es 9 CPA ,:-orga q ~:p Pa :n o ip h o ao yn~6 -0V 4 hi'" A -ah -6ffa,c vent as n T~ a CIL '~53 11016~: -Tul r4 n! '19 anuit Ch 40 Aithors s, Arb~ovp v Title I_; uots 6btiinid~ ~ i~: iiiAibh of g6AUM: salts of dieth*jt~iq~hosphoric- ' wqr.41- 6~ o"r Op _~IAN SR"' Otd Izy, k' ira ' ~ k inq 252,'Mir-A 1955 P; I Data M)': 66-s~a~c~ -r ardih 't ori--' t- )pe ids'of adi g g:_1 he: Aerivati and cer ain p;,,4 A d ' Q ste'xii, wlich-apped f-'ribnothiorlhos-. Ath t' 0- molecules 0 i_ o., S I . .:phoric ac id, and ofi d' poleculd of. i%obphcrous.LoId. The; doil.vation I of . e r, t ors , af the gc. lieral,fol of, codiura: salts m-, 16; ADF MI -5 (00 ~ 11~) 75)thioiv~,h the roacticn of _~ diotIv lthiop'hblh c ibcd -h-~rio doid wNh is, dov F Table. lnstltuiidnm: '2~_ ~i6md~ i Of: Do -j" AJSSI In.st, ~8 .ran -c h :I& yo htbuzz 0 v chow~tt~ mitted: Sub 1' 15- 19,54*,:: 7 soma -derivatives: of h dro hosobon c r IyAlkylp - Ath LA P .1. Souk Emu o" 47 44-61' e1" C:i' 47. get. 114 the futi"ing ~i)Et)j ~ud the datit ure given in the It -: P(o) rdeVs ~ yield. b.p,/mm., oV.-and dsi.1 , (Et%P(0)-' 1(18.8 1.), W.7 Ill N d jr. ethcr treated at rmn (et! With'15 ~IitoNpbt 'Ttbb Inixt. heated I 001, tWei Iteredi mid distd, yielded (,610)r PocArosr, (1)" 63-C- 100-70/0-51 1,4370, 1. (7.3 g.) caW oritW3.0 S. EtOCCHtDr 45 n gave Htlk and F$0jCCIIjP(0X0EI)0CAfr*R, 47M, IGIV; 11,4450, 1,1570; a similar reacticni, with RtI in a ~.!f(tujw. at tall-40 gave In 4 brs. EfF(0)(0FJ)0CAf#IR. 60.0, 141~-J.V/2, ]~.4305. lmm I (a Ij.) in W1. with 0.81 g. S icacted "otherink-ally and the to tt. heated at W- $)OCH", 68.7. 906 11110~ the S disaulvcd Save (kuow(. bt.j VMW/Wit L41176 1 1419 The same method was usmi fal the prcpn.:Z UtO,~POCHAhN, 78.12, ]DO- 10*/I. IOD-11) On ~Ilotbcr Wt of this rtkr this is Zven 1,4374, 1.0925; :~ Pro POCH OR, 60,49. 129-MI /1, 1,4305, 1.00 ~p-owo- C.11cMit, 40,05i 136;5~8'/L5,1.4435. I.M70; "o-ouo)r POCIMeR, 52.25,128~8.5*/I, 1.437.1.1.0345; ~1.'Iuuo POCA~R~ 48.12, IWl-7*/l, 1,43W. 1.02-M EJOI CII'Y c OXMOCINI R ;54.6.' 170-1.59/1, ~ 1,4425. 1.1761; Yh,k.' ~Slj MIX4'A, 1,4370, 1. 12M. Up(o) 01149 CH K 37.5, 140-24/0-5, 1.43M, LN 9; DOM' S)0 PIAICR, 14 3-0*/1. 1.4361, 1.1526; (Pro).- M)OC IAUR; 73A. -150-7*11 1.4550, 1.1106. (PrOhP. iocU.-ph; M.7. bi 101-2 /Ij 1.4598, 1.1017; (iso- I-OM3. 0. M. Kosulalloff j 77i P-1-1 -Y Mll-L 2 71 E~- Z~~ PAN Lai - A Ll MQV zvk~ - k - I . "P.*,sters ani Ester Auddes of Phosphoriep Thiopyrosphosphorlo, and Dithiotriphosphorle Acids and Some of Their Properties" ~'e paper present d at Nn r-irst Conference on Phosphorous Compounds, Kazan, 8-10 Doe 56 SO: B-3,084,841 -id orpnk d-erintives ~of vlAA arid , P Ell thiumm-e" iialtd.'i vathr-1 -4! -Adds of ~ii~,TJOrds. anti 'A 1b, V, r.;, -Iop. after I ar. a, 55.. Addod Willi -m '85, and 5ujuliug Oveluigtit.~ the filter Oln. IVRS di5td. Aelding 82 4% crude product, whkI, g2ve 14.2 g. pure 3 ' 1AS 15~M- d I OFZ7 b A 1 - - , t M , :, ID ~~V, ( Pf?~Inp, y, b, IW-1 5 bt 1829- 3', 14~75, I -*LV 173-4'. 1.4411. 134~A N, V. ' tit, bi 10-2 , 1.4&60, 1334 1.013, 2.1470. Thesc camp&, sbovrcd verv 11 ' 1, inw ficiliflixtivity0h thebarn wee%41. Rcactlo;! 0! (iso-PIO) NCI with Nil ditriv. imm 1C.0 g. (isr~ Pi 0: Nil-Nie a A 2.23 1. Na In ligir-Ine gni e91.3(, (rmIL and .1 14330i -S';mR4Ay werc Prepo., 43.1 E40):'p- ' 1 "( 81 M OFJ)xJ1A10-j-V, 1.44.1 ~Pro);P- 1204" O 4 5 b F e N m I , 1.4 0. . 1.112M. 11wtill Ms, j imled ttl))L ire nt I ~1 ve , Rtaction will DrCJ!zMM in I br. at 120,it)" sim0ark- '-gavc 1,419), I.MS; P.Odn. of 4.7 g. C('hCIIO to 9.1S g~ I w 1mve SpNit-leolm reactitill which yielil(NI 6111.b'', (Flo I'Mil; IM 0)(OROC/h M., ti. 162 ~10, I 11W. 1.3077, limting 6.0 g. In n-41 n.r.2 X. S in bV117cut. 20 lahl~ gave 64,02% 1 126 -7..,', 1.07131j.- ~;lmihltly wits InqA., (PIOW, (O)M- Z. ~t;: . Purl-aj Cf. CA 50,11231"i-, CH(OH)P (0)(OM)l (t~ WAS") and S.? g, V tsw I m). Ulroint was addid dropwl,-e 6.4 g alid thtsubctokept 1hr. at 65-70" to give aftcr filtrol Qnd j dillu. 100%, 0.9% ptirt Pr CRUM CTO, I Crude ptoduct of *.mvl- Pi 42, 10.40, shW 30 % a lpol -AeOH f4.-# distuw*;: the P-M&IS'll Int Of rent upou"', Wain Sir $227s).- AW lfi c 366; --wa, POW 0(0 41~ 1 0 d' ~42 Wfi"10 JW~Ob ZAVO 6 rwuct, ll~ IR-) a' ~aomxwy*o4 its 4 added, few. aropi of, tat i-14K'Na~Wolj and the uIxt. 96-4 1 ''tog -.'Akh in- 150 in]. lignine wai iKt;lttd 64h Q) I llIA4AtiNfblb-w In. of 10.0 t., llol~ i 14 by dropw6a hr. ut 05-70-tije inixt.- was filuml 67'~' ob 1--tAff. b,., 160-10. 1.41 137 -T 7" "0' -hamilwi bj JIM-7*) 1.41 anj,37.50 lli~?Tnftellim w Oth acyl' baj~drs* Is. hindered f by ~Vt 4 1 "do e c atom t, .1y bi i~um for cullipletion, E0 ivith eel 'and Ft,IN V A(6C(OAr POW -41 W-IF WWI 12, U, ax Sii . i I pd . P ALIMOV, P. I., zvzjlli~~%O I.I. Z.j ond FEDMOVA, 0. IT., (J'%. -". lul-,uZov Clicl-JC01 Ynstitute of rhznn "Esters and Ester-Ami&~!s of Phosphoric, ThiopYrophosplicric, Dith.-lotri- phosphoric Acids and Some of ~.Jjcir Properties," Khimiya i Primemenic Fosfororganichoskikli Soycainenii, pp 164-175, 1957 MA A.I fN,, .1A tu --v, ~Wl, VIC m P N MPI -M Han AITY1. AS USSIO "Esters and Ester Am-Lder. of Phonpl-Loric, Thlopyronhosi)horic, Dithiotriphosphoric Acids and Some of Their Prooerties" (Efiry i efiroanidy fo5pornoy, tiopiro'Losforr.-I-Ii, ditiotrifosfornoy kislot i 1.kh nekbtoryye svol,,-stva) Chemistry and Uses of Oxj&anqj&osphoraus Compounds (Khimiya i Primenenive f(Nsfo1=Uan1ehesk1kh sayedneniy), Trudy of First Conference, 8-10 December 1955, Kazan, PP- Published by Kazan Affil. As USSR, 1957 14,1- / /-f - Report. discussed bv D. E. Sh%igayev (Xinsk State 11"Odical InstitutO and. K. S. Shadurskiy (1',insk State Medillal Institute). ALINDV, P.I.: CHRPIAARDVJL, I.V. . ~ --l- _ - Mono-dichlorovinyl enters of some derivatives of phosphorus acids and their properties. Izv.Kazan.fil.AN SSSR.Ser.kbin. nauk no.4:43-47 '57. (MIR& 12:!;) Mosphorus acids) (Ineacticides) (Vinyl compounds) ALIMV, P.I.-, EWROVA, O.N.; CHEPLANDVA. I.V. Synthesis and properties of amidee of dialUylpboapboric kbim.nauk no.4:49-57 157. (Amides) (Phospboric some mixed and U-substituteid acids. Izv.Kazan.fil.AN SSSR.Ser. (MIRA 12:5) acids) -ALIMOV P.I.; FEDDROTA, O.N. Syntheses and properties of some di-N-substituted anidalboaphates. Irv. kff SSSR.Otd. kbim. nauk no.11:1985-1990 N 160. (MIRA 3.3:11) 1. Khimicheskiy institut im. A.Ye,Arbuzova Kazanskogo filiala. AN SSS:R. (Phosphoric acid) ALIMDVt P.I.1 FEDOROVA, O.N. Preparation of amides of N-phosphorylated aminocurboxyLle acids. Izv.Kazan.fil. AN SSSR. Ser.khim.naqj no.6t48-53 161. (MIRA 16:5) (Phomphorus organic compounds) (Amides) ALIMOV, P.I.; CHEPLANOIA, I.V. Syntheisee and properties of some dialkyl, p-chloi-oplieny:L-P-trichloroethy~ phosphlLtes, WLophosphites, and phosphines. IzvJ',azttn.j'il. AN SSSR. Ser.khim.nauk no.604-60 161. MRA -ktj,,~ (Phosphorus organic compounds) ALIMDV, P.I.; CHEPLANOVA, LV. Syntheses of some chlorine organic derivatives of' phosphorus acids. Izv.Kazan.fil. AN SSSR. Ser.khim.nauk no.6:61-651 161. (HIRA 160) (Phosphorus acide;) (Cgorine organic compounds) ALLICYs PI_ ------------- ;-- Products of -the condens&tion of chlorr-1 with orgarophoapil.oric acid rzdCes, 11.1,v, AN SSSR. Otd. khir. rp-,uk no. 1,.(Al-64 A 101, 14:2) 1. MAndchealdy ins'llitut im.i,.Ye. Arbuzcvz~ KL,.-anslogo fillc~la All &)SR. (Gliloral) (Amides) ALIMOV, P-I-, FFDoWVA, 0,.N.# CHEPLANOVA., I-IT- Synthesis of certain substoittted amidea aid mixed asters of phosphorue acids with possible pbysiological actvity. Khird~m i Pr'maneldyO FQSf0=r9MICbsZkikh Soyedirytnjy (r-beadstry and &Pl)licgtiOn Of OnlanOTIhOsPhorus comnounds) A. Y& jtq~aWDV, g4j. Publ. by Kazar AfInio Acade Sci. USSR,, Moscow 1962, 632 pp. Collection of comilet4i Papers presented at the 1959 Kazan C-.niference on Chemistry Of (;rgauoD)vsphorus CorwoundB. ALIMV, P.I.; ANTOMINA, L.A. Synthesis of some N-sulfen derivatives of dietkv:l phosphoric acid amide. Izv. AN SSSR. Otd.khim.n4 no.6:1132-.1134 Je 163. (MIRA 16:7) 1. Kamnskiy kh-Imicheskiy institut imeni A.Te. Arbuzova AN SSSR. (Phosphoric acid) (Sulfenamido) - A, L.A. ._~~IMOV, P.I.; ANTOKHM Synthesis of N-stibotituted amides of 000-aryl alkyl phaa- phoric and phosphorothioic acide. Izv. AN SSSR. Ser. khim. no.12:2204-2206 D 163. (MIRA 17;11) 1. Khimichaskiy-institut im. A.Ye. Arbuzova AN SSSR. ALIMUV,-P.I.;- IFVKOVA, L.N. Esters of mono- saml diisothiocyanophosphoric acids and their derivatives. Izv.AN SSSR. Ser.khim. no.ltl87-189 A '64. (MIRA 17W 1. Xhimicheskiy inatitut im. A.Ye.Arbuzova AN SSSR. D I chl orcmii thy I emt3 aratdmz o I' I i-hos" no. 5,,932-93,3 Mc,, *6,,,. y AN ALIMOV, P.I.,- OrOMINA, L.A. DerivEttives of di,~thoxyphosphorylamido-N-sulfanic actd. Izv. AN SS.SR Ser. khim. no.7:1316-1317 Jl 164. (HURA 17:8) 1. Khimichaskiy institut imeni A.Ye. ArWzova Ali SSS",", ALIMOV, P.I.; ISINKOVA, L.N. Phosphorylation of formaxide. Izv. AN SSSR. Ser. khlm. no.10t 1801-1807 0 l6k, Derivativea of metiyleneamide of dietbylpboaphoric.,aaldl,".,'bid.i 1889-1892 (;6RA'17t 12) 1. Khiml.cheakiy institut im. A.Ye. Arbuzova AN SSSR. aredi anct -reactions Id th SUIJ-W.;' nitrogen - (I~oxvle i-ethyl.. bromide j and -,C.Iiloral, were iri,ied ~oilt i:.4,46"etudy, tbe""'~uni Ai dal.'.`eff'eb't`-j- 12 isubstances 'here iiyntM Igiivpd_'~it~ A ft u - an :wWose"Compos im. ne u P, orw 7 iNid c~iU- th- f 6, *61 aijoimce x 1, e1 0 ;Af ast Z'd 'I !, . . lilt, A F .:'Akademi -nau)c r uzo a -- - -1 ~ ;--.- --l - , %fi*u-t6i-74c~ '-d a 7 . WHO All NCO 4,~,:-,'Synt mili toiil%stel 'ITLE, he ,yiene,~Ejmd&,or.j 0 -h ChI61 Vot, Tep ef (C614, em N --m 0 where CSTIV fAht t e Propy A ,j~h Imm, j71 . . ... . .IT UR/00~2/6 ilia/ .. 4 I or ocarboiilc and!i.6'' oc oni ylii6d iii~fthi id amb' c It lbh 'a iq~'-n65 7- '1965,~ 1098-~~ 0 P, ay Wd 60,ay eni.rami& of-diethyl.O oasph or tc 'acid -.with - bbh~- 16116hydr q* the rea0~,tl'onsj'4_:thiopr'l_ M-"" it- d4i afid othylen ame;:hci wiWPI.,opy nesium !brov de,'~vea(ll 1y rdacts v t i; s6diuili mereapt des bal I gpoups'. HSHII + M. rome. yene amide of diethylp;-~6sphorl~c acia. Otth i.--'jymb3e had lhe 'followin g, cour,~e: ... I I I I FROM ?OWA I I EMMA The reaction W-16--Siq-"c~lium (C4116% 19hp, G14 G + fit, - l dl l 40 1 1 ! 'bl4te-.,w (0) N Zoo 0 AC6 NRt .:V6032594 ~Wkt-ddD86S-UR/o 66 216-6 /0 C 10 10 08 / 1486/ 1488 AUTHOR*. Alimov., P. I.; Antokh!Lna:, L. A. ORG: Institute of Organic and Physical Chemistry ime A. Yo. Arbuzov, Mado:V of Sciences, SSSR (Instit-at organ!Lchoskoy i fizicheskoy khimii JU-cadomii nank SSSR) TITLE: Reaction of amido esters of phosphorous acid with acid chlorides SOURCEt AN SSSR. IZV-DStiya. S02-iya khimichos~aya, no. 8, 1?66, 1466--1488 1 TOPIC TAGS: phosphorous acid$ chloridet orpanic amide$ phosphonic acid, ABSTRACT: Reactions of chlorides of acotio, bonzoic and othyloarbonio acid with 0,0- dimethylphosphorous N-diethylatido produced corresponding derivatives of phosphoni.o acids ocul (C-j11&)jNP(01' 311s)j + RCOCI (C311s)INP + clig P\ 0 COR R:-r,[[,(I);' C,11&(11); -Cjlgopil) Action of the same Acid chlorielos on othyl, ester of phosphorous acid N,W-totraothyl- diamido can be repramited* as - follows s' Car 1/4 uDct 542.qi+546.i83.z-t66i.7i8.i 7ACC.NR# AR503259.4 oi, + j(G~llshNj,POGsH&+RG PGOR CsH&Q -j(Cjlls)&NjsPOCjI4 I(CallsNills Cl -R- ~.o *0 144MP" + Itc. A. **'OCH "OCN N(Csti&h opf +'RCON( HJ v OC,,Hl' R .5~C CGHO CjHsO N-diethylaminoadforqrl chloride reacting with.amido *star# forms proditoU of Arbwtovls rouTanipment in good A" OCHI (Cfft)*.NP + CUM(Coll" (GH,),NOI +CILQ OCHI Card 2/4 ACC NR; AP6032594 Tablo I gives the phyaical constants of the synthesized amides and axldo eaters of phosphonia acids. OxIg. art. has: I table. SUB CODEI 07/ SUBM DATEt 2'.?Jan66/ ORIG REFt 006/ OTH REN 002 Card 3/4 ,7.4ce7j4f~. AP60~Z591~--- I Table 1 1 * - I ., I B 1-. -0 1 .20 1 20 1: - , . [Card 4/4 1 ACC NRt AP6032588 ---------S-0URCj;-C-0-DF.~-W006,2-/66/000/008/1370/1373 .UTHOR: Alimov P 3*1.,-,, Fodorova, 0. N. OIZG: Chemical Institute im. A. Ye. Arbuzovp Acadomy of Sciencosp =-It (Khimichookiy institut Alcadomii nauk SSSR) TITIE: N-Phosphoryletion of glycino andsome of its dorivativas SOURCE: AN SSSR. 12;vostiya. Soriyakhimichoskaya, no. 8, 1966, 1370--1373 TOPIC TAGS: glycino, phosphorylation, organic amido ABSTIUCT: The phosphorylation of amino acids and their dorivativos is of intarost in! connoction wit-h the uoiogicza activity of amino acids, which in phosphorylated forms participate in metabolism. Ihe article describes conditions for the phosphorylation of glycino and some of its substituted amides. Yhosphorylated glycino.'; were obtained re by the action of dialkylphosphoric acid chlorides on glycino in water Ln the p sonco of a tertiary amino at ~, OOC: (H0j'i21'(0)C1+N11zC1i2C00] I+ (Cz11s)aN, (110) it' (0) MiCHIC0011 + (C1111)3N-11C1 R = C2115 (1); C41111 (11) Monosubstituted amidas of N-phosphorylatod aminoacotic acid, where the substituonts are various groups,vere obtained by the following reactions. The act!ion of hydrox- Card 1/3 1 7-a-64461. ACC NRI AP6032588 yl--'no on ethyl N-diothylphosphorylglycinato forms the corrouponding hydroxamic acid (C2H50)2P(O)NHCH2CON110H (ILE). The action of chloral or aqueous: formaldohydo on N-diothylphosphor lglycinamido produces respectively N-(a-hydroxy-O-trichloroothyl) (C2H;0)2P(O NHVH2CONH(;H(OH)CC13 (IV) N-hydroxymothyl amide, of the same acid amido 05 (CZH50)ZP( )NHCHZCONIICHZOH 1,'V). N-monomothyl amides of phosphoxylated.g3,voines aro formed by the action of aquoous mothylamine on the corres'ponding'esters (nO)3P-N-G11aCOOC61[j+C11lNHj- 0 R? (RO),P-N-CII,CONIICIls-FC2116011 0 R R c2lia; R, 11 (VI); C2115 (V11); R = i-C3117; R, Cill, (V[11). Disubstituted am-31des of N-cHalkylphosphoryl-N-othylglycines were obtained by the reac- tion (RO)3P-N-Ne+C1CH,CONR,'_(RO), 11-N --- C113CO.NRz'+NaQ 0 .R, 0 It where R, RI and RO are a3kyla. The physical constants and yields of disubstituted amides are shown in Table 1. Qrig,, art. has$ I table. Card 2/3 ACC NR, AF032,cS8 Tablo 1. Dialkyl Amidos of N-DLallqlphosphoryl-N-Ethylglycinos Bp, -C d Formula (p P% kijl 4 yo C.11.0),p -N-clitcol? (CIII)s 1 1,1076 1.4585 37.61 C. C.11 (0.5) (C il 160) t 1, -N-C I I IC 0 N (cs, 14) a 131-132 I,OG66 1.4569 47,1 C. M (C.1 F,O),l --N-CII,CO3(C,1 [Ab 144-145 1.017G 1.4542 62.0 (1,5) 163-164 1,0190 1,4670 67,7 (1) (i-C.11,0; M-11-CH&CON(c,lish 126-127 I.OMI 1,4515 63.4 1 1 0 (:,1 to q (0.6) 11-C,117O."I.-N C11,01)N(ca 11.4 I 146-147 o.9923 1,4525 45.4 . 0 It.11, (1) SUB CODEt 07/ SUBM DATEI Z5Fo7,:)64/ ORIG Wl 009/ OTH REF: Oll A-CC NRt XV7003487' kN) SO(JHC9 CODE: UH/Q,194/bb/LK)4/Vk/ULQ2/L "-d AUTHOR: Neklesoval I. D.; Alim2v, P. I.; Kudrina, M. _A..- Iraidava, I. S. ORG: Institute of Organic aa:7 Chemistry im. A. Ye. Arbuzov, AN SSSR, Kazant - 6is-ical -oy i fizicheskoy khimii AN SSSR) (Institut organichesk TITIZ: Relationship betweenthe chemical structure of certain iunido caters and imides of phosphoric acid arid their, toxicity.l., V SOURCE: Khimiya v sallskom kho2-,yayptve, v. 4, no. 6, 1966, 22-26 TOPIC TAGS: phosphoric acid, irLides insecticide, weed killer ABSTRACT*. 'About 50 amido efiteir3 of phosphoric acid and acylimidophosj~hatod were synthesized and tested under la!boratory conditions for toxicity to warn-blooded animals., insecticid4activity, and phytocidal proportics to ostablish the .possibility or,their use as insacticidos and determine the influenco of in- .dividual chemical ralicals ALpon the biological activity of the substances. The ,test specimens were whito vd.ce., granary weevils, house fUes,, and the bean Aphid. The most intoresting compounds were also tested on the rice-weovil,, 'the 8pider mitej gypoy moth larvae) and the migratory locust. Replacement of the OC2~2 group eituated on the phosphorus atom in amido esters of phoophorio noid'and soy2imidophasphatea b3r tho OCH group led to a docroaco.in the :~oxioity of the_ "imi 9 1 ioing"tho nd- idt.h-Tespeot o warm-bloodod animaley, jpqu... L 10787-67 A:dC .'len'gth of the hydrocarbon radical situated at the phosphorus atom in amido esters of phosphoric acid and a,-.ylimidophosphates lowered the toxicity both for warm-blooded and for invertdbraW animals. The diethylamido group L-1 amido esters and amides of phosphorus aoids lowers the toxicity of tho, compounds in comparison with the dimothylamide group. Whon the 0-2.2-dichl.orovinyl group -vas replaced by the 0-chlorcallyl radical in mixed eaters of phosphoric acidj the insecticidal properties of the compounds wore sharp3y reducod. -Replacement of the OxO-d ett~yl-01-(2.2-dichlorovinyl)phosphate~,,,by-tho 002H5 group in N(CH3)2 group lowered 'the toocicity of the compound for warm-blooded animals. When two OC2H5 groups in tho same compound were replaced by the N(CI,:3)-2 groupj, there was a further decrease in the toxicity for warm-blooded animals, a sharp *decrease in the contact activity, and an intensification of the By's4emic actioni of the compound. The presence of a double bond in the compounds botween the '.nitrogen and-carbon atoms (P-N-G) sharply roduced-the insecticidal properties ..of the compounds. Among the compounds studied, amidophosphatos exhibiting - .systemic properties with.rospeot to gnawing pests were doto6ted (SD,o for wwm-~ b1boded animals' was 8$T150 M.?kg). Such compound3 JnoIiidodC* O-mothyl-O- :(2 2-dichlo ov )-N-dimothylamidophosphato and D-qIiohlorQv-InyI-N r . irWI methyldiamidophosphate.e Crig, art, has: 4 tables. (JFRS: 38)9701 SUB CODE: 06s 07 SUBUDAM 16Sep65 ORIG PEN - 016 / 0111 REFt 006 ene'l ACC NRI AP7010721 SOURC& CODE: UR/0062/66/--DOO/008/1461/1463 AUTHOR: Alimov, P. I.; Fedorova, C; ' N'.' ORG: Institute of Organic and 11hysical Chemistry imani A. Yo. Arbijzov, Academy of SQionces USSR (Institut organichesicoy i fizicheskoy khfinlA AN SSSA) TITLE: Condo~sation of N-mothylolamidas of dialkylphosphorous acids %;Ith narcaptans SOURCE: AN StSR. Izvestlya. z-porlyp khtmichaskaya, no. 8, 1966, 14411-1463 TOPIC TAGS: morce; tan, condensation reaction, organic amide, carlx).Vlic acid P SUB CODE: 01~ ABSTRACT: The condeneation cif N-laethylolamides of dialkylphosphorous acids with mercaptans'was found to procced analogously to the correaponding CEXbWylic acid .derivatives, yielding N-alkyl.thiometbylamides. Bix new N-allcylthiomethylamides of dialkylphosphoroue; acid3,were produced by condensation of pr-oPyl,-J.s0Pr0PYl, and, butyl mercaptans urith N*zethylolamideG of diethyl-, dipropyl.-, diisopropyl-, and' diisobutylphosphox,ic aclis. The corresponding N-methylolamidOPhOGI)hates were pro- duced by the action of formaldebyde 6n smides of diaUqjphoj3.pboric acids (the alkyl rer.iduea being etbyl, propyll. iGOPrOPY1, and ig0butYl) and t1aat of Paraform on the N,-etbyl-amide of diethylpb~csphoric acid. Acyl derivatives ware produced by the Card UDC: 542.954 + 547.269.1. + 661.718.1 - - - - - - - - - - - - - -W411-mlge MUM= PM-xRvkxR&AWU-R; M-A ACC NRt AP7010721 action of acetyl ohloridD upon .11-metbylolamidophosphates. jr,4e p~yj;jcaj properties. '-pf all. the new -Aerivativeq. are. described. Orig. art. has: 2 formulas and 2 tablos. EJ-PRS**:' 40,3517 Card 2/2 ACC NR3 AT7001742 AUTHOR.- Al It, OIG: none SOURCE CODE: U1 i/000q4st76-66/666/66~ ~16~ TITL-.',: The third boundary ralue problem pf electrodynamics SO1P-.C.'..- AN KazSSR. Institu-to matematiki mckhaniki. Uravneniya matematicheskoy fiziki i funktsionallnyy mializ (Eclus,tions of mathematical physics and functional analysis). Alma-Ata, I--d-vo Nauka Ka%S,",I-',, 1966, 51-59 TOPIC TAGS: Maxwell equation, electrodynamics, electronic comDuter, boundary value problem, approximation method, linear equation, alGebraic equation/ M-20 electronic computer ABSTRACT: An approximation method, based on a variational method, is studied for the solution of the thiTd boundary value problem of electrodynamics. The experimental data showed that the electroikX;ietic phenomena can be described with sufficient precision by Maxwell equations. The third boundary value problem con3ist8'of calculating the electromagnetic field which arises. This ran be dono when the normal component of R and the tangential components of ff on the surface 5 are known. The solution then requiras deteruining the tangential component of Z and the normal component of H. The eleotromagtietic field satisfies the integral equation rot ~U(p,s)X(s)dS, Cord 1/2 ACC NRt AT7001742 where ,4nH(p)-iT,(p)+grad~U(p,s)l(s)dS- U (p. s) 7(s) dS. C WI(p)-grad((f)U(p.B)i(s)dS-i"-j UpdQ- 'SU!dQ+ ~U% -gsrj)dS. W, (P) rot S U7dQ -rot ~) U (g, dS, and U o0s k~ is the fundamental solution of the Helmholtz equation (A -k 2) U 0, in which 2_ wt. The Bubnov-Galerkin method is used for finding the approximate 08 solution of the integral equation. Since the problem is for a spherical surface, spherical coordinatev are used. The Liam coefficients also enter the problem. The conditions for convergence are: 1) the problem has a solution -.Ui space H; 2) the sequence of the coordinate functions is complete; 3) the coord.1nate ftinctions must be linearly independent. The solution is unique* This problem leads to a system of linear algebraic 2quations. One problem is analyzed (using an 11-20 electronic com- puter) with the help of matrix theory. Orig, art. bass 17 fortulas- SUB CODE: 12t 20/ SUBM DATE: 22J=66/ ORIG REFs 004 Card MO -- ALIMOV, R. Second boundary value problem of electromagnetic vibrations. Vest. AN' Kazakh,SSR 20 nooll:54-59 N 164- (MIRA 18:2) ALIMOVI R. -- Norms axe new, Imt deficiencies are old. Fin. SSSR 37 no.11- 30-32 11163. (MIRA 17:2) 1. Hachallnik uprairleniya Ministerstva finansov Kirgizskoy SSR. DONEETS,.S. (Rostcv-na-Donu); KUZIWN, A. (Iikiitsk); MEDVEDEV, N. I'Saratov); LICHKOV, G. (Arkhimgollsk); TSYPIN,,Ye. ISverdlovsk); GITCHENKOI 1. (Sochi); GRUZINTSHVA, A. (Novosibirsk); ALIMOV, R. (KIpa-J,4.a); GOLOBOR011OV, M. (,I;yktyvkar) Outposts of air transportation. Grazind.av. 20 163, (Aeronautics, Commercial) t nc,j,4t22-;V4 Ap (MM 160) CODE2 UR70-055765FO( ACC NRs AT6013422 SOURCE W0059 AUTHDR& -Alimov R& ORGs none 47 tion oil'. W! second problem of TITLEt, Intepral egv7r, P ie SWROE: AN Kea=, 19ektor mg,tenatiki, i mekhaniki. Issledovaniya po differentsialInym uravnenij~m I ikh primeneniyu!' (f,esearch on differential equations and their app3-.i- cation). Alma-Ata., :Izd-vo Nanki'S 1.965,1 ~4-59 TOPIC TAGS: integral equaticn.,.~leotrodynamics., boundary value problem; electro- magnetic fieldo vectvp coordAnate system .ABSTRAOTt The problin of deteri~ining the vectors 9 and 9 of an electilomagnetU fiela vhich satisfy the coAditions rott JrY, di'v -P rot gto -9 o M- in domain Q is exambiad. The, bowdary conditions on surface 3 axe 7~ (Its g, Cow 113 -2/3 Cos (3i)+.(Oi -p)] sln (3d9dy, oid C Jan u #ft~otlmssor IL IL sbab*tn Ogig 6D+A U~tmv at'd 30 Tom ~of soleaUfte and Pedegogiml Aotlvlir)s,t A. A. GWWO V.. A4. Tb:tVlmktys, M. A. Sbateloup R. A.. Allmovs, N. 1. Topavarkht M F. FWWlov* 0. R. RaMmip W 16. !Wklno B.- 1. SbabaUsh *MWrUldwstv*� No 1* V 92 Sbabeftla-bes vA14slmd mrs-Ibm 30 *096two works* most of thu damitad to the as'= of abort-alroult * PAWW379 ho has ebmA on do imar tranwimilon and has ~ direated staft" on Ung-d1sUmme pow tratemlastan IV do and gia at tho Power ftg X=tj, Aced S" Uzbek M Simbeftla le a WW~w of tho Penomt Cotimlasion con Sbmt-ClrmAt Curmtes Mb of Moo lbtw SlatUm.jo t1w Oomalasian an Imig-DUteme Fmor Tramolsoung Dept of Tech Sol* Aamd Soi US!IRp and of the Sol Oouwdl of the Sal Pm IImt of W, ALIMOV, R,A, IrTigation of the Golodnetya Steppe and research problems co"ected vith it 'Izv All Uz.SS2 no,.210-9 156, (MIRA(14:5) ""' 0 10 Chlen-korrespoudent All UzSSR, (Golodnaya Steppe,-Irrigation) ABALIYANTS, S.Ei., kand.tekhn.nauic, red.4 AL III, ALTLUI S.T., doktor tekhn.nauk, red.; Vr7,GO, H.S., red.; ZAPROICTOY, S.G., kand. takhn.nank, red.; MUKHAPCOOV, A.M., kand.tekhn.nauk, red..; NIKITIN, I.K., Imnd.tekhn.nauk, red.; POPOVA, K.L., red.; POSLAVISKIT, V.V., akademik, red.; ROSSIIZX:rY, K.I.,'Irand.tekhn.nauk, redo; URAZBAYNV, M.T,,1 doktor tekhn.nauk, red.: IVANYKKO, T.A., red.izd-va; GORIEWAYA, Z.P., tek-bn.red. [Channol processes and bydraulic enginnering; paparB of a coordination confernnee, June 7-12, 1,9551 Ruslovye protsessy i gidrotakhaicheskoe stroitolletvo; materia3,v koordinatsionnogo soveshchanita 7-12 iiunia 1955 g, Tashkent. Izd-vo Akad. nauk Uzbekskoi SSR, 1957,- 416 p. OURA 11:5) 1. Akedemiya nauk SSSR. Sektstya po nauchnoi razrabotke problem vodnogo khoziaistva. 2. Sredneaziatakiy politakhnicheakly institut (for Aballyante)o P. Hinisteretvo vodnogo khoz3raystva UzSSR (for Alimov). 4. Sredneaziatskiy nauchno-lusledovatel'skiy inatitut irrigatsil (for Vyzgo,.Nikitin). 5. Inutitut sooruzheniy AN UzSUR. (for Altunin, Eaprometov, Mukhamedov, Urazbayev). 7 Chlon-korrespondent AN UzSSR (for Alimov, Altunih, Vyugo). 8. A~ademl,va nauk trzSSSR (for Poalavskiy) (Hydraulic engineering) ".11 red.; YERRBNKO, Y.Ye., red.; ZAKIROV, K.I., akndetait,,red.; KANASH, B.S., akpdemik,'red.;.KUKHAMEDZHANOV, M.V., ekFidetnik, red.; HABIYEV, M.N., a-kademik, red.; RYZHOY, S.N., red.; SADYKOV, S.S.,red.; YAKHONTCIV, V.V., red.; BUGAYEV, V.A., kand.fiz.-mat.nauk,c)tvetstvennyy red.; PANKOV. M.A., prof., doktor sel'skokhozynystvennykh nauk, otvetstv-eniiyy reid.; KURANOVA, L.I., red. izd-va, GCRIKOVAYA, Z.P., tekhn.re.d. [The cotton plazit] Khlopchatnik. Tashkent. Vo'*.2. (Climate and soils in cotton growing regions of Central Asia] Klimat i pochTy khlOPIZO17kh raionov Srednei Azii. 1957. 626 T). (MIRA 11:1) 1. Ghlert-korrespondant AN UzSSR (for Alimov, Yeremenko, S!~dykov, Yakhontav). 2. Deystvitellnyy chlen Akademii seltskokhozyAy9tvennykh nauk UzISSR (for Yeremenko, Mukhamedzbanov, Ryzhov). 3. All UzSSR (for Zalcirov, Kanseh, Hukhamed2hanov, Nribiyev). 4. Vseso~ruznaya akndemizra ael'skokhozynystvenny1di nnuk im. V.I. Lenina (for KAnash, Ryzhov),, 5. Akeidemiya nauk Uzbekskoy SSR, Tqshkent;. Inatitut matemnt!Lki i mekbaniki. (Sov!Let Central Asia--SoilB) (Soviet Central Asia-Climate) (Cotton) KANASH, B.S., sikademik; KALITSEV, A.M.; VLASOVA, N.A.; PASHCEEKKO, Z.H.; ROZHANOVSKIY, G.Yu.; KAUM, FX; MOK313VA, Ye.A.; KLYU17Y, G.A.; BURYG3M:, V.A.; SHOTEM, A.I.; RUKI, V.A.; ROMAROV, I.D.; AVTONOFIOV, A.I., oty.red.; KUKHAMUZHAHOV, M.V., akademik, glaviyy red,; NXZHOV, 6,N., skademiki samestitell glavnogo red.; ALIKOV, R.A., red.; DABADAUT, A.D.# akedemik, red.: DZHALILOV, aIE-on*ns,uk, red,; TMMCMO# V,76.0 skedemik, red.; ZAKIEOV, K.Z.# ekademik, red.; KAMUNOV, N.M., akademik, red.; EABIUV, M.N., akademik, red.; SADYNOT, S.S., red.; TOGOTEV, I.N., kand.skon.nauk# red.; IMONTOV, V.T., red.; KURANOVA,.L.I., red.izd-va; RAKHMANOVA, M.D., red.izd-va; 3ARTSEVI, V.P., takhn.red. [Cotton] Khlo chatnik. Tashkent. Vol.3. tStructure and develop- ment of' cottoZ Stroanie i rasvitis lchlopchatnilm. 1960# 402 P. (KI3A 13:10) 1. Akadamiya na-tik Uzbekskoy SSR. Tashkent. 2. Akademiki UzSSR (for Kanash, Mukbj3mdxhanov, Zakirov, Nabiyev). 3. Vaesoyuznava akademiya sallakcikhozyaystvannykh nauk imeni V.I.Lenina (for Kenasil). 4. Tsen- trallne,ya selektsionnaya stantsiya Vaesoyuznogo neuchno-i.Beledovatell- skogo institute khlopkovodstva Uzbekskoy ekademii sel'skc&hozyaystven- nykh muk (for lanash). 5. Tashkentskiy sellskokhozyaystvannyy insti- tut (for Malltsav# Shleykher). 6. Inetitut genetiki i fi2dologii rastenly AN UzSSR (for Vlasova, Mauyer. Klyuyevq Rumig Romonov)e (Continued on next card) KAHASH, S.S. -.-- (continued) Card 2. 7. Sredneazistvkiy gosudaratvennyy univeraitat (for Pashchanko). 8. Institut bot-aniki AN UsSSR (for RozhanovBkiy, Mokeyeira, Burygin). 9. Chlany-korrespandenty AN UsSSR (for Avtonomov, Alimov, Teremenko, Sadyko7, Takhontov). 10. Usbakokaya Akademiya sol'skoklLOZYS.Vstvennykh nauk (for KWdwmedzbariov, Ryshov, Dadabayev, Yeramsnko, Zakirov, MannanDv). (Cotton) RESHETKINA, Natallya 14iklaylovnaj ALM, R,,A., otv. red.; ROMANIKA, N.A., . izd-,val- BARTSEVAt V.P., tekbn. red. izd-vaj GLYSMSKAYA, red. [HydrogeologicaLl principles for planning vertical draing.ge in the Golodraqa Step;bk] Gidrogeologicheskie osnovy proaktiroveniia ver- tikallnogo drerazhi v Golodnod, stepi. Tashkentj, Izd-vo Akad. nauk Uzbekskoi SSR,, 1960. 141 p. (MIM 14 t 9) 1. Gblen-korrespmlent AV Ilzbekskoy SSR (for Alimov). (GDIOdWa Steppe-Drainage) KARASH, B.S.. ukademik, otv. red.; MURDAKOV, T.S.; kand. biol. nguk, otv. red.; QUAANOY,'G,Ta-', kanA.'biol. nauk, otv. red., UINI- LEY3T,,Kh.Kh.v*doktor biol. nauk, oty' r9d.;'HTMXWWOV, Me, Ocademiko red.1 RYZHOV, S.N., a~ndemik, red.4 ALDWY, _U" rod.; DAROATM, A.D.._ekademik, red.; DZRALIIm-'-.1"H-.R.. kand. elcon. naulti red.-,*YMEK=O. Y.Ye., akDdemik,, red.s, ZAKIROTp K.Z., skademik, red.; RANIUROV. N.M., skademik, red.; KABITRY, M.N., akeaemiic, red.-, SAWKOT-, S.S., red.; TM13T, I.N., kaind. ekon. nauk, red.; 'TAKHONTOT, T.T., red.; POUT, Y.Goo kand. sell1khom. nai*, re4[decorjeedl; RAMNOTA.M.D., red.; BARTSUA. V.P...tokhn. red.; KAURAYNTA. Kh.U.. tekhn. red. [Ootton] Khlopohaitnik. Tashkent. Tol.4. (Phvsiolo&v and blo- chemistry of cott6n] Fisiologila i biokhimiia khlopohatnilte. 196o. 704 p. (RDLA 14:5) 1. Akademiya nauk Uzbekskoy SM. tashkent, 2. Akademiya nauk Usbeksko;,'SSR (for'*~khemedzhanov, Kanash, Zakirbv-, 11abiyev, Yakhontov, Yerermako) j, Usbakskays*a1cadamiya sel'skokiwayby- stvanifth nsi*'( for Mukhomedshanov, Ilyzhov, Dadabayev. Yore- menko, lZakiriov, Xannan~v) 4. Chlen,7-kQrrpspop4entY Ali Uz&M-, (for Alimov, Uremenko, Sadykov, Yei6n'tov-) 5. viesoyusuayll aka4emiya eel I skolchopysystvennykh nauk'Im. T.I.Leninn (for Kanash) (cotton) YASEVICH . V. K4 y prof . Ii KHODIYEV , E.M. j assistent; VAVILIN, M. K. ; AKAIAYEV, N.Kh.y* B~RZUIKO, A.A.p ordinator; ALIMOV, -R.A.; RABIRWICII , S.A.; TSENER$ Kh.Kh.; KOKOSOVA, T.A. - Angio.,-ardiography in the diagnosis of congenital vitia cordis. Mod. ,;,,hur. Uzb. no.10:10-16 161. (IJIPIA 14:10) 1. Iz fakulltetskoy khirurgidheskoy kliniki sanitarnogo i pediatri- cheskogo fakul'totov (zav. - prof. V.K.Yasevich) TsslLkentskogo gosuderstvennogo moditainskogo instituta. (ANGIOCARDIOGRAPHY) (REART-ABNORMITIM AND DEFOINITIES) ALIMOV ~ it. A. Quick method for the staining of blood platelets. Med. zhur. Uzb. no.3:20 Mr 160. (IffiU 15:2-) 1. Iz Nauchno-issledovatel'skogo instituta rentgonologii, radiologii i onkologii Min.isterstva zdravookhraneniya UzSSR (direktor - prof. D.M.AlAurasulov). (BLOOD PLULLETS) (STAINS AND STA114114G (I-LIGROS COPY)) R.A. Alimovp 1902- ; on his 60th birthday. Izv. AN Uz. SSR. Ser. tekh. nauk 7 no.lt82 163. (MMA 176) ALIYOV, R. Sb., aspirtint. Experimental observation on com-powid antibacterial thezapy in tuberculosis. 11.4ed. zhur. Uzb. no.5.*72-77 Myt63 (Mlim 17:40 1. 1z TSuntrallnogo histituta taberkulesa ( dir. - prof. N.A. Sbmaltry., nauclr%7ye rukovodltelil - prof. F.L. Minson i ,~rof. V.I. Puzik) Ministerstva zdi-avook-1Lrwimiya SSSR, F iT. -.,f JP w~ CT Uztekskog.,, OURA 18:8) n;~i t.~ita r,,ntpetj,olcg!i, V ALWOV, R.Z. "InveBti:7ation of Beat an(] Mass Exchange In the Fvaporation of a Liquid From a Peated Cylindrical Surface in Transverse Flow." Cnnd Tech Sci, Kazan Aviation Nnstj Kazan, 1954. (RZhMekh) Oct 54) Survey of Scientific and 17echnical Dissertations Defended at USSR Higher Educational Institutions (10) SO: Sun. No. 481, 5 May 55 f.1 C V SUBJECT USSR CARD I / 2 PA - 1356 AUTHOR ALIMOV P Z. -;Fe- r afer on the Occasion of the Transversal Passing of r TITLE Ire a n a Two-Yaase Flow !Round a Heated Cylindrical Tube. PERIODICAL Lrn.te.,hn.fis 25. fasc. 6, 1291-1305 (1956) Issued: 7 / 1;53' reviewed: 10 /1956 The present work deals with th,) heat transfer on the occasion of the transversal passing of air containing extremely small droplets of water round metal cylinders. Owing to the difficulties arising in connection with the aforementioned conditions the experiments were carried out with simplifi-ed conditions. Order and method of the experLuents are desoribed on the basia of a drawing. A liquid (distilled water) was pumped from a pressure vessel through a purifying filter to a centrifugal strain-?r under a pressure of 2 - 110 atm. The drops of water leaving the centrifugal strainer drop under the influence of gravity, taking the air with them. Hereby a two-phase cylindrical flow with a diameter of up to 1 m is produced at distances Of up to 0,5 m from the strainer; in this flow the metal cylinder to be investigated was located. The water was collected in a vessel, purified, and pumped back into the pressure vessel. The test cylinders were made of duraluminium rods of 12, 18, 22, 25 and 40 mm diameter, and were heated from within by an alternating currents The temperature of the surface of the compensators and tea". cylinders was measured by means of thexinopiles. Con- sidering heat transfer by radiation, there was good agreement among the results obtained at all surface temperatures, which indicates that the apparatus used is V I Zurn.techn.fia, 26, fase.6, '1291-1305 (1956) CARD 2 / 2 ?A - 1356 well suited for its purpose, Conclusions:. According to th-9 temperature of the cylinder surface, there exist two different kinds of flow round the cylinders and of heat transfer: a film- like and a not wetted kind. Transition from the film-like to the not wetted kind takes place if the temperature of the cylinder surfaoe is somewhat higher than the boiling temperature of the liqutd, and by this transition the intensity of the heat transfer is considerably reduced. Experimental results are here re- presented in form of generalized quantitative dependences. However, because of the special character of the experimental method employed several. quantities entering into these relations are indirectly determined by computation. The process investigatod is suited for a variety of technical applications. Above all the film-like flow may be most effective for the purpose of cooling highly heated surfaces. In the case of not too large REYNOLD numbers (of the order of from 300 to 5000) and in the case of a moderate consuntion of liquid, it was possible to conserve a heat flux of up to 150.000 kcal/m , hour and a heat transfer coefficient of up to 1700 kcal/m2.hour.OC~ This is 30 - 35 times as much as in the ease of a flow with only air. This work is of great practi- cal importance for the gas cooling of reactors. INSTITUTION: L 0) Category: USSR B-13 Abs Jour: RZh--Kh, 140 3, 1957, 7703 Author Alimov, R. Z. Inst Academy of 15ciences USSR Title Concerning One Type of Stable Free Surface Formed by a Heated- Thin Liquid Film Orig Pub: Dokl. Ali SSSR, 1956, Vol 109, No 3, 559-56o Abstract: A film of thickness 20-200,." is formed on a horizontal metal cylinder 22 mm in diameter which is placed in a current of water droplets 50- 1110,,.t, in d.ameter, freely falling under the effect of gravity. If the temperature of the cylinder does not exceed 800, the free surface of the filin remains snooth. At temperatures above 800 annular pro- jections are formed along the cylinder; an average of 1.7-2.0 projec- tions and trough are formed per centimeter length. This state is maintained up to tem eratures in the neighborhood of the boiling point after which all the liquid evaporates. The formation of a wave-like stable surface in the presence of considerable temperature gradients Card 1/2 -5- ALIMOV, R.Z. Stable forms of free surfaces of thin layers and fine itrope of heated liquids. Izv, vyse ucheb, zav.; fiz. no.2:144-150 158, (MIRA 11:6) 1.Xazzanskiy aviattionn" institut. (Idquids) (Surface chemistry) 69322 I 0.5-000 s/147/60/000/0'/011/018 C022/E535 AUTHOR: Alimov, R. Z. 7A TITLE: - _Gn' _t_1_-,e_M_y_ T i -a Wt mr-of the Process of Heat- and Mass- Transfer utring Evaporation Coolinf-OT-57ronglf Heated Surfaces-00 PERIODICALt Iz-vestiya vysshikh uchebnykh zavedeniy, Aviatsionnaya telthnika, 1,96o, Nr 1, pp 94-103 (USSR) ABSTRACT: The paper di~aals with the problem of "perspiration" cooling1whiah is considered to Lie the most economic method of cooling, in which it is possible to neglect tho non-productive losses of the cooling liquid in the form of droplets separated from the bulk of the coolant and carried away by the gases (see Ref 1). The analysis tatkes into consideration mutual inter- dependence of the heat and mass-transfer. The presence of a foreign substance moving in the transverse direction through the layer adjoining the surface alters the hydrodynamics as well as the physical properties of the boundary layer. As yet, there is Card 1/ 9 neither a reliable theoretical method nor sufficient V1( 69322 S/147/6o/ooo/ol/oli/oA E022/E535 On the Mechanism of the Process of Heat- and Mass-Transfer During Evaporation Cooling of' Strongly Heated Surfaces experimental data to enable us to deal with this problem. The existing results are contradictory (Refs 2, E, and 16). Since there are no reliable data to indicate that the temperature field changes substantially when a diffusing stream is present, this effect is neglected in the article and only the changes in the coefficient of thermal conduction of gases in thi? boundary layer and the effect of these changes on the heat transfer are investigated. The processes of heat- and mass-transfer are assumed to be confined to the boundary layer only; furthermore, it is assumed that the fluid, the thermal and the diffusive boundary layers all have the same thickness. The radiation heat transfer to the wall is neglected, so that only conductive beat transfer is considered. The mass- transfer i;s assumed to be entirely due to diffusivity. The! treatment is one-dimensional, Starting with the Card 2/9 hea.t flux per unit area from a plane A of the bound