SCIENTIFIC ABSTRACT SAPOZHNIKOV, YU. P. - SAPOZHNIKOVA, R.G.

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December 31, 1967
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SCIENTIFIC ABSTRACT
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~T L 51844-65 EWVm)/FWG(m)/EWP(t)/EWP(b) IJP(c) RDVI/JD/JG ACCES-SION NR: AP50liBO9 I-rP/'008()/65t'038/004/0717/0720 546.23+546.65 AUTHOR: Markovskiy, L. Ya.; Soboleva, M. S.; ,a2zhnikov, Yu. P. TITLE- Preparation of rare earth selenides by reduction of selenites SOURCE: Zhurnal prikladnoy khimi v. 38, no. 4, 1965, 717-720 TOPIC TAGS: rare earth compound, selenide, lanthanum compound, cerium compound, praseadymium compound, gadolinium compound, neodymium compound, reduction method k ABSTRACT: Selenites of lanthanum, cerium, praseodymium, neodymium, samarium, and were reduced with a mixture of hydrogen and hydrogen selenide at 600-C, 5-lenides of the general formula M2Se3, Hydrogen selenide was used to the F-~r7o_ti-_)n of oxyselenides, which were present In the reaction products W-11 11. 11_1~_Igen al-ne was used. X-ray phase analysis of all products sbowe~ .ra-if-us I an t han, im s~ Phases 'in the czwe of each rare metal. The powder figures for i-arium palvselenides had the same system of lines and nearly the same inten- t -a" Jlffe:,ed in nterplanar dist-3nces. Such J15taTICeS f,.-r the'pcwder pat- --rr~F - :lolyselenides of cerium and the other rare earth elements occupy an inter- Card 1/2 25(6) AUTHOR: TITLE- PERIODICAL: ABSTRACT: 11-larJ 1/2 SOV/9--59-5-19/27 Sapozhnikov, Yu.M., Engineer On Thermal Efficiency of.Steam--Poi,.,er.Installati6ns of ST Type (0 teplovoy ekonomichnosti parosilovykh ustanovok tipa ST) Energetik, 1059, 1Tr 5, pp 32-33 (USSR) In small enterprises not conneoted with outside thermnl and electric networksi the themofication aggregates of 5T type work in accordance vith electric chart and their efficiency direG-tly depends upon parameters of used steam and the graphs of steam loads. The author examines how to find the most economi--al consumption of steam by means of a U"' balance equation (.T N c-r-( int t n-is' C'L r-K -Nlr~v. (int- K wb-erein --AM!"i-c' the utuillzod heat oC used steam, SOV/92 -.qg-5-19/27 On Thermal Efficiency of Steam-Power Installations of ST Type and d are specific expenditures of steam. d or ST anti 'K In kg/e.'.s./hour; N., ancl IT are ck viers of ST and SK h%"r-slopo --11; p C, .0k n. r7. -re temperaturel- of fead wat-'r El. - e,, of tho boiler amd locomobiles ST anal SK in 0; i is the cont-ent of heat in overheated steam K of both locomobiles in large calories per kg; 1j, is the content of heat of saturated steam from the boiler, in large cal'ories per kg. The Lyud-J-- novskiy loicomobil'nyy zavod (Lyudinovo Locomobile Plant) is mentioned in the texct. Card 2/2 A f ~.ftnn r07 COLMUGUUCX QW ZZ-VP- A Wal L Wation W. Mde. &AL.R. 85622 IZO% IZIS, 110%5 B/078/60/005/012/003/016 13017/3064 AUTHORSs Markovskiyq L. Yu., Sapozhnikov, Yu. P. TITLEj Some Properties of Lead Selonite PERIODICALt Zhurnal neorganicheskoy khimii, 1960, Vol- 5, No- 12, pp. 2655-2661 TEXT: Lead Belenites were prepared by the following m,-.thods: a) Reaction of lead nitrate or lead acetate with potassium selenite in the stoichiometric ratio, b~ reaction of lead acetate with a solution of seleniousacid, c reaction of lead nitrate with an excess o f selenious acidq d) reactiorL of lead-carbonate with selenious acid. Acid lead selenite Pb(HSeO 3)2,was formed by the methods b), c),'and. d). Lead biselenite PbSe 0 was prepared by heating Pb(HSeO The 215 3)2 to 130oC best method of synthesizing lead selenite is that of precipitating from a solution of lead acetate with selenious acid or potassium selenite. After the synthesis, the following compoundB were separatedt PbSeO37 Card 1/3 85622 Some Properties of Lead Selenite S/07 8/60/005/012/003/016 BO17/B064 Pb(HSeO and PbSe 0 Moreoverythe double salt PbSeO Pb(NO was 3 2 2 5* 3* 3 2 separatedv and its occurrence confirmed by chemical and X-ray phase analyses. The lattice parameters of the compounds are given.,Microphoto- graphs were taken of the individual forms of lead selenites. The thermal stability of lead aelenites was studied.,The-differential-the=al curves .were determined with an EIIV-09 (UP-09) recording electronio potentio- meter, and with an OK-54 (-FPK-54) Kurnakov pyrometer. The thermograms of PbSeO show two endothermic effectst the melting point lies at 3 675�1000, and SeO2 Iforms at 790-8300C. At 4-10OCp a strong endothermic effect appears on the thermograms of the double salt? indicating the de-, composition of this compound. When further.heatedp the reaction product melts, and at 690-7000C Se02~vapors form in a considerable amount. An, endothermic effect appears at 110-1200C on the Pb(HSeO 3)2 thermogram, cor- responding to the dehydration of this compound. On further heating of the dehydrated product, SeO vapor is generated at 3800C. There are 6 figu.'resg 2 3 tables$ and 17 referenceag 9 Soviet. Card 2A m 20020 S/081/61/000/002/006/023, 2L,1 o 11 AOO5/A1O5 Translationifrom: Referativnyy zhurnal,,Khimiya, 1961, No. 2, p. 320, 2K101 AUTHORS: Markovskiy, L.Ya., Sapozhnikov, Yu.P. TITLE: The Development of Cathode P=osph~�rson~ Basis of-Certain Metal Oxides PERIODICAL: "Sb.tr.Gos. in-ta prikl. khimii" 1960, No. 43, pp. 92 100 TEXT: The expediency.of the application of mineralizers to the synthesis of the lum:Lneseenoecomposition MgO.-Cr:LiC1 is shown. It is found out that the composition MgO:Cr:LiCl has.relatively low emission intensity in thevisible spec- trum range and is of importance only as an i.r.-emitter. The lumineseerm compo- sition Al 20 -Cr has high emission intensity in the visible spectrum range (X max 690 mt) ana*does not yield to the lumineseerxe composition Zn Mn with res- (P04)2: 0 peat o the-magnitude of the relative emission brightness. 2:b sh6wn that it is possible to obtain new luminescerm compositions with.a. wide emission band, a large part of which lies in the red spectrum region by mixing oxides of Zn and Mg. There are-13 references. R.A. Translator's note: This is the full translation of the original Russian abstract. Card 1/1 29532 S/078/61/006/011/010/013 BIOI/B147 AUTHORS: Sapozhaikov,---Yu. P., Kondrashev, Yu.~D.f Markovskiyj L. Ya., Omellchenko, Yu. A. TITLE: Study of phase composition and luminescence properties of the system ZnO -MgO,,ac'bivated by chromium PERIODICAL: Zhurnal.neorganicheakoy.khimii, v. 6, no. lit 19611, 2550-2 557 TEXT; On the ba sis of.A.paper by A. L. Smith (see beio'#) who at udied the luminescence of nonactivated MgO 'and ZnO miktures,-the authors examined the syst.em MgO -ZnO activated with 0.5 ~.of Cr (added as ammonium bichromate). The mineralizer added was 3 % LiCl. Samples were produced at 1100 and 13000C. ~ Powder patterns were taken by.a YPC-50-~4 (URS-50-I) apparatus. Two limited solid solutions were found: Zn(Mg)0 and Mg(Zn)O with the structure of the.initial components. The unity cell volume of the solid solution Mg(Zn)O increases continuously. The ,incorporation of Mg ions into the hexagonal structure of ZnO causes a slight increase of parameter a and a considerable decrease of parameter c; thus, the unit cell volume is reduced. The upper limits of existence of Card 1/3 Chromiura i Sq S/078/6i/006/011/010/013 Study of phase composition and.i. activator of ZnO and of solid Zn(Mg)0 solutions. A paper by G. S. Zhdanov, V. A. Pospelov (Dokl, AN SSSR, lit 97 (1953)) is mentioned. There are 4 figures, 2 tablest and 10 references: 4 Soviet and 6 non- Soviet. The two most recent references to English-language publications ,read as follows.~ A. L. Smith, J. Electrochem, Soc,, 55, 155 (1952); W. A. Runciman. US Patent no. 2736712, February 28, IT56. ASSOCIATION: Gosudarstvennyy institut prikladnoy khimii (State Institute of Applied Chemistry) SMUTTED September 30, 1960 Card 3/3 ACCESSION URt AP4029185 9/0076/64/009/004/0856/0866 oir I'AUTHOR: Markovskiyp L. Ya.; Sagjqrhn.Lk Boyev X. Is TITLE: Bismuth Selenites SOURCE: zhurnal neorganicheskoy khimii, v. 9, no. 4, 1964, 856-866 lenite, synthe is, composition, the Bi sub'V TOPIC TAGS: bismuth se s rmal stability, (Seo sub 3) sub 3, bismuth selenite, bismuth selenite monohydrate, Ri sub 2 (Seo sub 3) sub 3,11 sub 2 0, Bi sub 2(SeO, sub 3) sub 3.H sub 2SeO sub 3, Bi sub 2-1 (SeO, sub 3) sub 3 SeO sub 2, BL sub 2 0 sub 3.SeO sub 2, Bi(NO, sub 3)SaO sub 3, Ai sub Z(SO sub 4; (SeO sub 3) sub 2, Bi(CH sub 3COO)SeO sub 3. thermogramm V bismuth s ous acid, crystal mLcroph elenide, BiSe, Bi sub 2Se sub 3, seleni oto- graph, x ray analysis ABSTRACT: The conditions for synthesizing bismuth selenites, their phase composi-i tion and thermal stability were investigated., Reaction between H2SC03 and bismuth nitrate, sulfate, acetate, chloride, susp nsion: of bismuth oxidesp hydroxi. I ide, basic carbonate and,cLtrate were run. The Matence of the neutral selanits BL2 its monobydr&teAL2(3603)3-H2O and its crystalline acid "it (Se03)3, i Ca'd r 1 ACCESSION NR: AP4029185 is best prepared~b Bii(Se63)3.H,SeO was confirmed.* BL2(SeO )3 y.reaction, of~ c,3 bes se enLous ac d with bismuth nitrate or trate. Two new selenites Bi 2(SeOj eO3 and B12O3.SeO2 were identified, as well as selenite double salts with nitric, i sulfuric and acetic acids: Bi(NO3)SeO3, B12(SO4) (SeO3)2d' Bi(CH3COO)SeO3- Hicro-IL photographs of these various selenites are shown. X-ray at& is given. The thermal stability of these selenites was investigated (thermograms; are shown in figs. 1-6) and explanations are given for the various endothermic and exothermic, effects observed. The bismuth selenides:BLSe and Bi2Je are formed on heating 4. the.noutral or acid bismuth selenitee in hydrogen or calbon monoxide: Bit (560s)o + 914 2BiSe + 911g0 ~vw Big (SeNt + I)CO Dlfse~ + FA Orige art@ has: 8 figures, 4.tables and 2 equations* 2/8 's, ~ -- - ACCESSION~ NRt AP4029185 INCLOSURE 1 01 A OC 40C q me V JV0 Off jog IM 1w 700 AV AV Joe jw AV IV ix -M AV. w -M, 1 12 If 21 JO X 'a M W'I 6AZ, W/),. Fig. 1. Heat curve for the neutral bismuth Fig. 2. Rea t* curve 'for the neutral -selenits BL2(Seo3)31 Gad BL2 (SOV. 3 bismuch selenium oxide BL2(SeO3),3*U2O Card 4/8 L 1-0532-4~ EWT(m,)/ (b) 'r ct EWP ACCESSION NR: AT4044996 AUTHOlk SaiDozhnftv, Yu. P* TITLE- The crystal'bydrates of neutral cadmium selenite and their thermal decomposition SOURCE: Leningrad. Goi;udarstvenny*y,inbUtUtprMadwykMmll, TA**---n* 51 -100C 1 1. . 0 & - P , - Khimiya I teldmologlya lyuminoforov (Chemistry and technology of lundu9j*rs) 3449.'~ TOPIC TAGS: luminophor, cadmium'selenh fe,leadmium selenite, ned'racidmium. selenite, crystal hydrate, cadmium selent Trieduction ABSTRACT: Since the usual method of preparing CdSe lunitni6phors involvios the high- temperature reduction of cadmium selenite by hydrogen, it appeared Important to the thermal stability of the various pbases of cadmium selenite and Its hydrates. In the present paper, the crystal hydrates were obtained by reacting a solution of eadmimn sulfate with a stoichlometric amount of sodium or potassium aelenite after the preliminant i-11 nf I // 10 Vie statchlometric amount of selenious acid. After 10- 15 days, colorless A Cdrd 1/2 M qj L 10539~~t6~ ACCESSION NR: AT4044995 obtained, which are attable at rdom t6inperature. The lattied parameters and chemical romposition of these crystals and of a(-CdSe03 are tabulated. Heating of these crystals t 1 ()0- 11 QC fo r one hour also did not change thel r phase or chemical composition. At higher temperatures, however, endothermic dehydration took place, witi, acdgeOLL-2-HY12L . . . -`- -4 __.__ff1i6 nhanfrincr 1RAV. -1V -d 2- thbWo gin --i--cwmtwd-eq-u L I' ASSOCIATION! (7.613 emV*y bmutut prms of-Vp1led Chemi2!aj ~41-B.WTTED: 00 ENC14 00 W 004 OTHER: 003 SUB COD),-: IC 2/2 Card , . . I ~k- , ~.., I -., . 1 " Ml of to ## k# 0 0 $1 to a 0 it #j to 0 Pipe 0 1 i~l 0 4 1 0. fffa IOLA 1 0 4 L t. ~-Jt% 00 ' 1. 4, t 4v 4 . A 00 go irl T a1 he abimmal stUnk"M d bakeemll OMP V with Bra lives; ' 1-66 . mid Ulm - 1060111111ml bakpa ottopewift. A. A. Petrosr vao-~ J S., R,) CAM S C94 (U ik k F S A (Y), Is. 182." (deconspas.). has W4).S-. d: 1.9196. * 91!6 JJW5 4V 1JIM KOH convert, V i to At , so . . . . . o u . apott wid . 7. 4" M 8409.37).-In compils. 411 the type RCHICXbR 09 a, d b X . - -, ". n j (VI),,b. 1214 uji's, I* 1 %4% dko 1.410911. 40M 1 V1 U; -00 .. i Y IN kcltgxcx..R, whets the = - CIP1 :- te 9' c"m aa tb I ) h I loV . . o sand Ill. 4ivr 2.4 -7,11,14psawomo. 1 4' b"i"N"' (VII) M TI With KOH hi l V1 i 1-60 of e - " or ~ am. "W" gars. than t ShLf d he I hick permits the I or ' it = '=Z. when that cam &. P ~ - - - , t r da s y Asain A xnall amt. of the 1101SUAll Product, 2 -C!l~ hr;W,-lf-butadicne, is probably Mettent SlElft a ~zlqo a ~ 400 . sa j ' a reductive apfitting of so a KOH k d i h = , resinous film mpg on the wags after standi IV d = a- w s . mtr t , m arkh fannation of bypolmlitt and an h B I . an m. 5' ICI give (vM) b 09 r occurs, or e 00 t 2 bad . . ts-a . 1 I vM - e. oiefin. instead of the normal sevu. of hydro whieb obutallft dib 00 2 3 f - . d. IMW. xV iAw. VM and KOH forin 9 and it not h KOH i d C - rom or= Butane (1) adds Bra to . .3; romo-24sat- (n) idd 24 OH enoug . s use Hla. This abuse, . the Presence of KIO It a d lCl i i - t to y 00 Sams HRr with K l . n ve a ol xt, of the g s Thb bromirAtes to 2,2,34ribramobutane wbich wil i-r- MeCHICCIBrAte and %lcCHClClBrMe which ~ ! -dibronso-24mtene (IM. With 00 KOH gon entirely to 2.3 V7 1 !,d- KOH ti%*$ TV from the Ist and i#~ .a Bra this lonns 2.2.3.3-tetrabro-obutanc. 1 0- , 4 The Product of the unisn 4 U and I& i% M again with alkau. Sinxiiarly I Mist CIS form 2.3- t, KOH convercis to 2-chistro-2-butesse 00 di l i b ok; jo Mixt- of XftCHlCBrtMc and NfeCllllrCBrlltc (M. U ith KOH tbc~ form U and M From the rj&tiTr =00 - r s oro u . ItUlts. Of the reaction products, It appears tMt k-A th M f an the mixt. is nL % o H. M. Leicr~stcx~ zoo 'I ASSS-SLA MITALLUIRMAL 4.11FOATWE CLASUPKA11010 too to- %1*111.1. : xj~ 14111321 .9p 0- As a :s a 6 4T itt- a K K & at I M 0 0,60,00 00 0-0 o 0 o g ol g *eggs 0 a 0 000-0 so a ? A it F AN, JS -OR 1_1_ L -t A K r Z 00 A Costioarm and Loa. A ussian)-CII.MICK (5 S.) and 5.4 00 isoprelle In 15 ml. MePh, fit the presem of 0.06 g. at 135* v t be h b d i t 18 b 9;4 00 rs. c s ra e n u ,.w w. p V11% mixed 4- oad 00 bw 94-6*, d:* MOM. oV 1.47. M which an hydrolysis by - N*01 I pvt 11151' ak mised acids Into 5 s wpd 3 g . . . , q. . , acid. m. 0V (from JIO d il b b1 th I M 5 Af O roe - I- a g. o . o e t enw, ), an y s y V r4XI-2 d:* MU5 d tio R f 6 t 0 . e uc n o , m X. ho nitrile mist. In 15 ml. EtOll by 5 j. No pvt the corre- ' I* IW7* i i PA) li $ 73 I I d 67 A ) a - w w m . . s. ng a, x opm, . ( N@ , . , . c ' * 00 1.491U*. pknW, m. 160-70 . Iteatint 5.6 g. WPM, o~ V b I i M C l W s few out C I and d.X g. p ene (coutg, a Cll,: pery % ul"One) In seziled trjn* fornt) in 20 mi. McPh (with byti tralls 9SOMers; on stAnding, a small sunt. OF the tra ftsfolo, * o 00 tubes 0 Ins. at 135* Save 467C 2-MrAl, -j-CY4xoCYrjOh,,_ p In-53 0romitO),seps. Hydroiysbolaw. &UA& with 1 t. d.0 0.93M, %V 1.4700 (further beating .5 C. NaOR in dill. ale. 4S Iles, at faux pve 1.9 g. tram we 12 lavs. at 180' gives an "1n1. 0.3 F.), indicating that m' ;,Lid. bw 137,5-8* 34-40* (crudeY. m. 63* (from MO). ' ' I I he cis form does ntA react. The rutrile is rob, M a leatiffir 1.5 C. i I trite (obtained from C lc~~ at. 14), d ti t ) 3 b i :V mixt. of ck-(rans Isomers; 9 Jr. nimile and I V i Oll d 10 il d 12 l i 20 H i 11 0 f ll d Con ensa on LN- emp. ra. w th aq. au gave. amitle, an. and t eis " b 1=4 Or! 2 . t an . tr uxe owe m m irs., o n , ' r"Ur 159-M e 3 b l f th EtOll v 2 m -- w. w , mV 1-47W. Redurtim of the, nitrile S.1 0 $ by 4 oe , . mova o e e X. a , go y r , t While aridifWatiOn OF the filtrate cove 4A S. a6d bw .) N;A in ' '~S 1111. Ktol I gave M(n . b-O' 137 d:1 LMM %V 1.4740 alak-h is a mixt.,01 cis- b" 7(1.5-7% d:* (1-01w, mi; OM a . . . . 101.w (from M011). G. M. K Poe LITINAT4111 C1.011FOCATION Cr ditiala"Cl *e' &U _ V -4-i- T P 1' U ' , aea Nit its Kalf 11K1 an 4 o ~09000000000000000 o Zo * 40 a 0 0 0 0 * 0 0 0 0 0 a 0 0 0 * __ a a M M 0 : 0 000,0oosooooooooo,~o e 4 0 0 0 0 If 0 OA: e,0, -0 1 -0-0 0 w* 0 0 a 6-W MARKHININ, Ye.K.; PAPOZENIKOVA, A.M. 1. Vaesoyuznyy institut zashchity rasteniy, Leningrad. BEKHTEPMA, M.N.; MEDVEDEVA, G.A.; POaFZCVA M.N. i SAPOZHNIK Up G.A.,-~~,:- FEOFILOVA, Ye.P* Rapid method of detecting bacterial Infection in culture fl during.the produetio of treptomycin, Prikl. biokhim. I n (MIRA mikrobiol. 1 no. 6:726-730 N-D 165. 1. Institut mi ohiologii AN SSSR., Submitted Dec. 24y 19(40 -Z W -k, SAPOZHNIKOVA, L. V.; YEGORSHPIA, L. A.; EBERTS, V. L.; SBEROVEROVA, L. P. SAP07.HNIKOVA, M.A. (MoRkva) ORteonalacia in a man with Iranconifs syndrome [with summary in English]. Arkh. pat-20 no.4:81-86 158. (MIRA 11:5) 1. Iz patologonnatimicheakogo otdeleniyn (zAv.-prof. A.V. ISmollyannikov), Nnuchno-issledovatel'skogo institutR imeni N.V. Sklifosovskogo (dir.- zasluzhenW vrach USSR N.M. Tarasov) (METABOLIC DISEASES, case reports Fanconi's rachitic synd. with osteomnlacia, postmortem pathol. (Rus) (OSTBOKALACIA, in Fanconi's rnehitic synd., postmortem -pathol. (Rua), Cancer of the esophagus developing after Imrns caused by caustic soda. Vop. onk. 9 no.11:91-,95 163. (MIPP 18:2) 1. Iz patologoanatomicheskogo otdeleniya (zav.- daktor med. na-A N.K. Permyako-v) Ilauchno-issledovatellskogo instituta skoroy pomeshchi imeni Sk-Lifosovskogt) (gla-myy khlrurg instituta- chlen-korres-pondent AM B.A. Pal.-rov, dir.- zasluzhemlyy vrach UlrSSR M.M. Taraz~ov). Adres avtora; Mo8kva, I-101 B. Kolkhoznaya ploshchead', 3, Nauchno-iasledovatellskiy institut skoroy p0moshchl imeni Sklifosovskogo. KPMEVSlaY, N.A., pro".; Proceedings of the Mosco-4 Society of Pathologists for the First half of 1.964. krkh. pat, 27 nc,5987-94 165. (MIRA 18-- 5) 3. Frodsedatell Moskovskogo obsbahestva patologoanatomov (for Krayevskly). 2. &-krotarl Mos~ovskvgo obahchestva patologo.- anat,~mov (for 9apczbn-4k,-,va). ft -; I I ~ 1 -11- 111. 7 ww"9 owevow 1 , 9 Is 11 t? a W 777 1 2 L AL I, we" 00 it on" i A.P471, Ha IM 00 NSCI ~ the of 00 0 ride. V0101:41 uItY out rot 00,3 :3 d"V" 1111 gwvwcw with in 00 activit] = 0 :0 S min. in be dMi of the m Wig M on, OW the "a effort W is L A SITALLURMCAL 4,11111,11101 1" l j W am .4 O It sa V u it A. -0 As 0 oio 0 0 0 0 41 0100co S I 'Gab 0,000101ill 1.011 1 fts PMOM se We" Sao MA of of 1, 1Y 00 Pother a& OAb"1kO am Z A K & ; Y , . . .. . " _ V Chm- 1U* 9__S R') I ' 116-23(19&1)~-Thc ' 00 N&O.. 0. 114" mw xBo + Ka in 0.1 N Ji . ad-NA411% b W119010, KO + 91904 and WS.80, in b.1 W Rom Vim, Otisied, The , Octiou Velocity "Othkies for "A 6". of Chlo. kh suffstes in iocid it". them It A dwe"Ing with cub addit. of sullate but after a comm. of. t l i h b h 4d d f - w mos t a urt ty a a. out I At is reache - i1; f t l i d [H h f W ltl us on. O t ~ Caloc t iongit o M ty d KWA 16 th i 1 44 i h t f th i h 0, w C o e act v e t t a 10 1OV ty to solitaire. 'rho Ohn"Of of late gj by,itto 14 "bows n4w)w go slit fair M a "M -" 6 ! , of the . with .j hilt the astrement it w with the adda. of sulfates. Salta such " KCI. 1 MCCk do we give a lowering of the specd with a aA ccuens.. boonce It fullaws tb&t a low cannot I ftor the cliame of speed with change of activity I or hw Ow wAsr cbmige of activity of the aster. * 40 Wy It is k~ bist ~=dtstlvvly It b4o am i lk d : not a- 4 atm Ww"Whotbolossm ftPess. lya nert a PON. iolect Whib CWDFWO slaw down , 0, , Theme risswis an AMUM to those (tv the he ftm# it*$ no cut-saw by"Yolo. lught I ton Vaphe summowbo, the datit (cw ctincut. ot ag from 0 to 4 N and of Will Im" 0 Ill 3 N. P. It. a "'mail CLASO '"VION W, -081 on L S a of a .1 0 W a 2 6106910009 000,0.0 Ole 0 0 0 0 0 0 0 9 of 0. 0 *to * 0, 0 Sao** 90 & 0 0 0 0 0 dTOO -777ii-ST io v u 00 I water-solif acetate- 40 00 N. v mad Z. 0. Liatt 9"(19m D .00 06 it , ).- ats are - f 50POR w the i0crom fis the b. p. of EtOAcwaw wAm. t 0* a Oiwd bV' nks. The vahm of a - aw. immic 00 a we: D'S MOO I.M. N~AG,.10Mo 1j0, Mg".- 490 .47. !% MGM7AfO 2.42 mW Sm"",O 3.9 A, I 4 OWMI iR ON lack to MPP*o the Dw*v., 00 MbV~msrr.(C. A. 19. 12k)- Rathagwo zoo 410 Ar i t Iti, u 0 A, oac 9141114"C" "till OK 4-1 Its I a ada a a I w a a a a 3 1 v 14 1 1 '", I-, 0 0 40 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 C 0 0 0 000 * 0 0 so o 0 o 0* *0 #$I Aso Imp fifum Plocings Aow "It -W w F ~7 Fmi Poll In $Wad"$. d -00 13, ~ jected to ~nwwtwft 15* gall 26'. - The enalics . ga, of acovatin WIF4.*4 CK Rtot- sot Col.; CHOCKMNA I 4+ N&* + MCI. 16-50 A i 7xA m CE6clcooN& + m i M N U 0M = OO o 7 T 04 + 4 C=. Cod For the 090 . '" GOO 00 3 somm-alibi Wma amd ussol, the mte de- 6 ;W 0-, , 0 Fag, aim 0.5 Jr far both gemn the mo. a SOO -h- 008 for on. lot nd Ad 86"m of impas. me 11-65 will 9.78 Cd. ot 11"Aff-mod , -H t z M c Por cNam : + E - 36A5 Cd. tot X Cl. gold 22.37 for X - 1. *0, Not UPI 1-1 L A NITALLUNAAL UMAIWI DASWICAIM See owing IrO, voloso WAF MY cog Issul"mogf, mm Aw low All too- - 03 1, we a a Ic A * 0 0 40 so 1 so so 0 0~6 004 0 0 0 off to 4,00 00 0 0,000 00 0, 0'0.* 0 0000 a of 0 .0. .... ...... SAPC~ZIPMKUMI 1"'. tj. --l' ~, "-ltt-,. i" "-, ~- 1-11 - r- 11 ,,. V. iffff"t"t S'll ,111411 ~`, ... S/53/60/003/003/019/036/XX Bo16/BO58, AUTHORS: Dariyenkos N. I~, Sapozhnikova TITLE: Kinetios of the Nuc~lecphilic Substituti-cr. of Halogens in Halcgen-substituted A,,etates and the Influence of Halogen A-;cumulation a' the Place of Subst.f.tution on- the Mobility Df the Halogsn PERIODICAL: Izvestiya vysshikh uchs4bnyk-h zavederify. Khimiya i khi-micheskaya tekhnologiya, 1960,,Vol~ 34 No- 3, PPz 46+1 46r- TEXT: it was the aim of the authore to characterize the inf luence of the halogen a coumulating a' the substitut`cn pla,,e in a comp-letely quantitative way. They -~~ve a similar characterist-to of the. influence C of the haloge r~_ on its mobillty in r e a c t fc, n n natu s of nucleophilic sunstitution during the interaction ---)f the halcgen aceltatea with hydroxyl ion, and ammcmia. Sinciz the corresponding data by c-ther Ecien- '-istls for the reantion: CH HalCOO OH CH 'OH)COO'- + Hal- (1) differ 9 9 Card '/4 I Nucieop~-_'Ilc Subst"u' K4ns',fts c S/1:~3 6010034100310191036AX 9 n - .5 u b s t it e d c;;)3 f Halog-~nB ~n Halo- Acetate5 ana the Influence.cf Halo.-an Acrum-ulation EL' -the P I a SutstitT.-ztioa or the Mcbiltty of the Halcgen Mor widely, -,he authors determined fo-- this reaotion ""he ratty constants 0 Several tqmperature val--aes bstw,;.,!~n 6o qnd 96 C. Or, the basis cf -~he Fituno halogert iv~etatonl the ron,t.ion wan atudie(l wli,h- anotshor nualoar reagens, i.9. ,.-iqup, 4 a d 600C. The number of -ous ammoniac betwo(ar, ^5 r, c.hargss remains unshanged in phaae (I ) which determines the rea3tion rat;--- bu~ a new di4stz:I'but-_'o,-t of the ~~harges in "'he intermediate complex :~ccura, One r_~harge -~_f the hydrcxyl-ion is t.ransferred here to the ha-loger: H-0 + GH 2CICOO H-O.... C .... C1. H0I'H coo (2) O-C__0 At the ammonc~lyais; partial -charges in the antermi2di-,ate comr-lex: H H 454- + ITH + CH CI (31 3 2 'COO H N....C~ ... C-1 H N CH-COO + ei 3 1 Card 2/4 Kinetics of the Nucleophilic Substitution S/153/60/003/003/019/036/xx of Halogens in Halogen-substituted B016/BO-8 Acetates and the Influence of Halogen Accumulation at the Place of Substitution on the Mobility of the Halogen develop in the phase which determines the reaction rate. On. the basis of these data, the authors characterize the kineti,-'s of nuclear Bubsti- tution of the halcgens in mono-substituted acetates in dependence on the nature of "he halogen concerned, in the following way: 1) In the. reaotions with the hydroxyl-ion and ammonia, greatly differing with re- gard to their mechanism, iodine is much less mobile than bromide (Table 1). 2) The authors proved that tbe.ammoi.o1.ys1s reaction is ateadily SIC-Wed down by the acoumulation of .,-.hlorine -r. the chlo_~Jlne aoetates, since the activation energyincreases (Table.3)- 3) The periodicity" by P. Pet-renke-Kritohenko (Refs. 5,6) concerning the in flaer---%e of halogen accumulation in chlorine acetates on.the mobility of this halogen in the reaction with alkali, was confirmed.(Table 4). The authors presume that the lincreased reactivity of chlorine in. trichloro-s- a~7;etate is connected with''the change of the reaction mechanism, They did nc-t succeed yet in studying the nature of this reaction (its pro- dvt~ts, phases) more closelyi The authors drew the above conclusion from the aralogy with the data by J. Hine (Ref.7) on the increased reactivity Card 3/4 Kineti3s of the Nusleophlliz~ Substitw.ion S/153j6O/OO3/003/019/036/XX of Halogenz in Halogen-substituted BO-,6/BO58 Acetates and that Influsni,;e of Halogen Accumulation at the Place of Subatitution on the Mobility of the Halogen of +,he chlorofoi-m in the rea,-tion. with alkali. They mention the paper by M. B. Neyman~ V. B. Miller, and Yu. M. Shapovalov (Ref.8). Thsre are 4 t-ab'_11-pa and 11 references: 5Soviet, 2 US, British, and 3 German. ASSOCIATION: Urallskiy politekha-icheskiy institut im. S. M. Kirova; Kafedra fizicheskoy i kolloidncy khimil (Ur-al PolytechnIc Institute imeni S. M. Kirov; Chair of Physical and Colloid SUBMITTED: October 2,1, 1958 Card 4/4 I . . . . . . . . .. . .. ACC NR. Ap70081J3 SOURCE CODE: ~_R/6620/67/172/00L~1083 7_/0840~ 7, AUTHOR: Androyev, S. N. V. ORG; leningrad Institute of Textile and Light Industry in. S. X. Kirov (Leningrad- s kiy institut tekstillnoy i legkoy promyshlezinosti) TITLE: Coordination equilibria in the system Cu~"'-aq HC1 H20 SOURCE: AN SSSR. Dokla 67, ~37-840 dy, v. 172, no. 4, 196 TOPIC TAGS; copper compound,, absomtion spect coordination chemistry, chemical.;.. rum equilibrium OUC14 .ABSTRACT: Electronic absorption spectra of the crystals, Cs2CUM4, 1(CF,3)41112- th and 1(C2H5)41N12CuCl4, which differ in the size of the cations located outside e a iu coordination sphere, were studied. Thespectra showed that a decrease in the r d S!, 2 of the cation outside the sDhere causes a shift of thb absorption bands of [Cu C141 ions into the high-frequency range, the form of the spectral absorption' curves re-a maining the same. This leads to the assumDtion that the electronic absorption spectrum of the system Cu?-+.aq - HC1 - H26.at-C ~-12 M is due to the formation HCl of tetrahedral complexes [CuC1412- in the solution. 'A change in HCl concentration from 10-4 to 20 M in.solutions of salts of divalent copper involves the following processes: ? ICU (H20),113+- ICU (Hj0J13 C11+ - (CU(1TM0hC1.21:;t ICU (H20)3C131- ICU (H2OhC41"-tr'"S +_ (CUC141t -i-IfIA114-1 ... CUCI$.. Card 1 /2 13nc *. Aj e. A4 0 A~A-jf-t -,,z --l- 1--. - I I - . - I I - - li MW/ Chemistry Spectral ar~,:- .......... Card 1/1 Authors Title Submitted SAPOZHNIK Hicroclimate of the classroom and its significance for the condition of students. Pediatriia 39 no.1:45-49 Js-F 156. (MM l0a) 1. Iz otdela gigiyV Hauchno-icaledovatellskogo pediatrichookogo institute RSFSR. (CLIMATZ, microolimate of class-rooms, determ of @ff. on students) (VINTILATION class-rooms, eff. of microclimate on students)