SCIENTIFIC ABSTRACT SPITSYN, N.A. - SPITSYN, V.I.

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December 31, 1967
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SCIENTIFIC ABSTRACT
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BAYKOV, S.P., kand. teklin. nauk; BELETIKO, I.S., kand. tek-Im. nauk; BELKOV, S.F., lmh.; BELYMICHIKOV, M.P., inzh.; BERNSHTMT, I.L., inzh.; BOGORODITSKIY, D.D., inzli.; BOLONOVA, Ye.V., kand. tekhn. nauk; LIROZGOL'j I.M., kand. tekhn.nauk; VIADIMIROV, V.B., inzh.; VOLKOV, P.D., kand. tekhn. nauk,- GERASIVOVA, N.N., inzh.; ZHUKHOVITSKIY, A.F., inzh.; KABAEOV, M.F., inzh.; KALEVTSOV, V.M., kand. teklm. nauk; KOLOTDMKOV, I.V., inzh.; KONDILWYEV, I.M., inzh.; KURIETSOV., I.P., kand. tekhn. nauk; LIVOV, D.S., kand. teklin. nauk; USSIMNKO, I.Ya., kand. telchn. nauk; 1,11AKAROV, L.M., inzh.; CLETVIK, N.D.,, inzh.; RABIM, Ye.G., inzh.; ROZIIDESTVENSKIY.p Yu.L.., kand. tekhn. nauk; SAIWONIKO, I.M., lcand. tekhn. nauk; SIDOROV, P.N., inzh.;,SPITSYN, N.A., prof., doktor tekhn. nauk; SPRISHEVSKIY, A.I., kand. tekhn. nauk; CHL"IKOV, V.T., kand. tel:hnnauk; SUrN, A.S., kand. tekhn. nauk; 1111BERG, N.Ya., nauchn5ry red.; BLAGOSKLONOVA, N.Yu., inzh., red. izd-va; SOKOLOVA, T.F., tekhn. red. [Antifriction bearings; manual) Podshipnilci kacheniia; spra- vochnoe posobie. Moskva, Gos. nauchno-tekhn. izd-vo mashino- stroit. lit-ry, 1961. 828 p. (MIRA 15:2) (Bearings (litachirery)) SPITSYN, N.A., doktor tekhn.nauk, prof. --- ... Nonskidding belt drive. Vest.mashinantr. 43 no.2:40-42 F 163. (MIRA 16:3) (Belts and belting) J ACCESSION NR-. U 4 AUTHOR: Spitayn, X. A.; Tayp1yano2j.L.!-j Gorshenev H. A.; Liberman, B, 786 Eymovetst TITLE:, Method for checking ifrict lion bearings on a stand for Uniting speed. Clams 42t No. 1641.9.9 SOUICE: ByulletenO izobrateniy Itovarnykh znak-ovj~no. 14, 19641 64 TOPIC TAGS:. antifric t2iff- hamber Translation;____~~Eeit for checking antifriction bearings on a stand for- Jimiting speed in a testing machine with.meebanical or hydraulic loading and temporally stable lubricating conditions. -In order to cut down on the length of time and the labor spent in testing the test is carried Out on one and the same small lot of bearings, for example ten units,, which oper-.' ate at speeds which are increased by steps. They are tested for no less than twenty-four hours each until there Isan average rise -temperature. :of.40-500 above the ambient temperature.!-. 777 A-SSOCIATION: Veesoyuznyy nauchno-ins'lidoviatellskiy konstruktorsko I-tekhnologichiliiii ilistitut podshipnikovoy promyshlennosti.-UlkU7412B Scientific Research Della and t:-,.%. -Seppp-P-1 0 al Institute of the Bearincr Industry TIED: 0 SUB CODE: IE SUBMI 1/1 NO RU SOV! 000 OTHER: 000 JPRS Ord C L 06321-67 -EWP(J)/Foj7~.qi) __jJ c) 11DJ 6004034 SOURCE CODE: UR/0277/65/000: AUTHORS: Spitsyn, N. A.; Atras, S. G.; Tazhibayev, S. D. . -\\ - . 34 TITLE: Ball bearings which work without lubrication at higher speeds /3 SOURCE: Ref. zh, Mashinostroitellnyye materialy, konstruktaii i raschat detaley mashin. Gidroprivod, Abs. 9.48-357 REF SOURCE.-- Tr. Vaes. n.-i. konstrukt.-tekhnol. in-ta podshipnik, prom-at , V. 309), 1964, 66-74 TOPIC TAGS.- self lubricating bearing, ball bearing, solid lubricant, teflon ABSTRACT: Based on the work of Soviet and foreign authors developing self-lubricat ball bearings\/6nd on the experimental work performed at MIM, the following conclusions are reached. Ball bearings with massive separators made of teflon 4 and a special lubricant are acceptable for unlubricated operation under-aTm-ospheric conditions at normal temperatures. They provide a useful life of 100 and more hours at a speed parameter of d-l' IL n 40 000 mm/rev/min. Lubrication is provided by gradual wearing of the separator. Characteristics of a failing unlubricated bearing are increased noise during operation and a rapid rise in or-~rating temperature, measured on the outer rings (by 10-15C or more), -which is due to destruction of the Card 1/2 UDC: 621.822. LIREHMA&I, B,Ya.-. Si-'lT,'3YFi, N.A., dc)kllor takhr, nauk, prof.,, re,. - [~7achines for testj-ng antifriction bearings] MashiiW d1la ispytanii podshipniko-,r ka-cherdia. Moskva. Mashinostroen-e, 1965~ 151 P. (MIRA M3) zpj THIN, ll~ N. j i bU 'L C ri ar.1 ran-~ h red--'mrki~d bank v,-.1,- f 701ga Valle Yl. -ruziln a -,ch, r ap .,-.raya lab- I. Voigogradskaya cblfoitnay~l L It I I YA y A L 3565-66- -E'IIT.(M)/EWP(W)/EP-F-Cc)/EWMAI)/EWP-(i)/-T/EWR(t-),~tWP _WP(b) ~Z ACCESSION IM: AT502,2677 MD11M TG7SRM 5 0240 AUTHOR: Spitsyn,, N. A. -JonN n wear in high speed ball be ring s TITLE: Fric a operators SOURCE: AN SSSR. Nauchnyy sovet po treniyu i smaz)mm. Teoriya treniya i iznoda (Theory of friction and wear)* Moscow, Izd-vo Naulm, 1965, 240-243 TOPIC TAGS: ball bearing friction, ball bearing wear, bearing separator/ BrAZhMt,a 10 3 1.5 bronze/alloy, BrAMN 10 4 4 bronze alloy, No; 36205 ball'bearing ABSTRACT: The friction and wear of high speed (dcpi2.> 1 600 000 M rev/min) ball bearing separators are discussed. The gyroscopic torque of the ball is given as M, 15 1 0-10d.,?!~~sin which requires an axial-load of 1,15 10-"d.,n'1qb- sin! to damp out the-gyroscopic rotation of the ball (where d ball diameter). lt,~ b was found that the~y6irim= force on the separator does not exceed Card IA L 3565-66 ACCESSION NR: AT5022677 (see Fig. 1"on the Enclosure)-and that the yearlpattern oii the separator can be decreased by more accurate sizing of!baUs and slight length increase of the ball nest. In thrust and radial-thrust bearings.at-high speeds the centrifugal force drP -~- db Cos, F=~,28-104 2d d CP_ on the separator cross-connectors can be substantial, particularly i~,Xhe ball nests are of insufficient size. In unlubrieated ball bearings teflonPand self- lubricati mnaterialklseparators have been foundjeffective (for e:a5le, ball bear- t _T 00 ings N6.00-5a, a oad of 8-10 kg and 8500 rpm,were found e a life of 3 hours, using teflon-separators). Tests performed at VNIIP a variety of mate / rials at speeds of d b = 1 425 000 - 1 814 000 mm rev/min have shown that CP BrAZhMts 10-3-1.5 separators with s~4el connectors are best for single-row radial a ball bearings, while BrAZhN 10-4-4ggeparators are beat for thre int radial- thrust bearings (see fig. 2 a and A-espectively on the Enclos 0 Ori art. urX .90 has: 2 figures and 1 table. ASSOCIATION: Nauchnyy sovet po treniyu i smazkam, AN SSSR-'(Scientific Committee on Friction and Lubrication, AN SSSR SUBMITTEDs 1NEY65-- SUB COM JE NO REF SOV: 000..- OTHER: Card.2A I -L 3565-66 ---. 11. 1 1 1. I I ':.- AccF,ssioN NR,. AT5o22677 ENCLOSUREs' 02, t I... t Card i -- -- SP IT SYN, N. 1. _,._'_____..l._,,_ I.- - " Department of chemistry. Trudy MGRI no.26:6o-62 '54. (MlRA 8:12 ) (Chemistry--Study and teaching) LAPTEV, Fedor Fedorovich; SPITSYN; N.I.. redaktor; SFMWWA, N.A. rodaktor; POPOV, N.D., tekbnIcheBkiy redaktor (Water analysis] Analiz vody. Pod red. N.I. Spitsyna. Moskva Gos.nauchno-tekhn.izd-vo lit-ry po geologit i okhrune nedr. 1955. 143 P. Kim 8: 10) ( Water--Analysis) ALITOVSKIY, M.Ye.; CPAPOVSKIY, Ye.G.; BABUSIIKEIT, V.D.; BILIDEMAIT) if N:j LAPTEV, F.F.[deceased]; SOKOLOV, I.Yu.; CHALISHCBEV, A:M deceased]; FROKHOROV S P 10KAREV, AJI.; KOROTEYLI'vy A.P ;ABRAI-110V S.K.; KONOPLYMSEV, A.A., red.; PRIKLOMSKlY, V.A., red: deceasedi; SPITSYN, N.I., red.; MARBOV, N.A., red.; ------=I,IONOV IN., red.; LYUBChMKO, Ye.K., KULICHIKHRI, N.I., red.; red. izd-va; POTAPOV, V.S., red. izd-va; GUPOVA, O.A., tekhn. red. fffydrogeologist's handbook] Spravochn4 gidrogeologa. Pod ob- shchei red. M.E.Alltovskogo. Mo3kva, osteoltekhizdat, 1962. 615 P. (MRA 15:7) (Water, Underground) 1. 3PIll'i'L71, P. D. I Enry. 2. USSR (6no) 4. 311-aft Sinking 7. Determinina the depth of bla-st I-Iole in sk-inin-a vertic~-d uzine shafts. Uiwll 28, 5 - Q NO. 1953. 9. Monthly List of Russian Accessions, Library of Congress, 'Ray -1953. Unclassified. __L_ 59283-65 EVIT(m)/EFF ACCESSION NR! AP5016568 TJR/0153/05/008/002/0263/0207 "THOR: Zaboyeva, M. I. Spitsyn, P. X - _21 ans of differential spdcl ro- TITLE: Determination of large quantities of n1obium by me photometry SOURCE: WUZ. Khtmiyalkhtmicheskayatekhndloglya, v.8no. 2,: 1965, ~203-207 7- TOPIC TAGS: nioblum, ~ioblum compound, spectroph6tometry, m-d termination* - niobiu 9 phosphomolybdate complex ABSTRACT: The determination involved the use of a-reaction forming a phosphora to establish the op-! niobium-molybdenum complex (PNMC). ThIe object of the study was timum conditions for the formation of PNMC at highnioblum concentrations. 1he effect of various factors * on the formation of PNMC was followed by measuring the optical density of the yellow form, of this complex in sulfuric acid solutions containing oxalate and tartrate tons. The optimum temperature was found to be 20C (at higher temperatures, only apbo8phorus-molybdenumcomplex (PMC) is formed). The formationof PNMC was complete in 45 min. The optimum content of phosphate, NaZ"04,42HgO, and mdybdate, (NH4)2MOO4, was also determined. The IbIlowing elements were found to Interferevith vanadium (0. 5 the determination of n1oblum: zirconium and titanium (above 0. 1, mg) rd 1/2 SPITS-IP1415 V,A, Autc,matle mii-I fcr icngt-itud-Inal-apiral rolling of twist D -3 14 12 (Rolling mills) s/122/61/000/011/00-2/006 D221/D301 AUT'HOR- Spitsyn, V, A., Engineer T 121uh A new high-j~roduction method of manufacturing t,,iork- pieces with a helical profile PERIODICAL- Vestnik mashinostroyeniya, no. 11, 1961, 50 - 54 TEXT.- The author developed a new high-production. met-h-od. of helical cross-rolling of components with a profile as used for spiral drills. This can be applied to diameters from 1.5 to 12 mm or more- It consists of a single pass rolling of the entire profile by one or two pairs of opposing rollers, inclined in respect of t Ile blank by an angle corresponding to the helice of the drill. Fou_r rollers in theoworking position form a closed drawing plate of the profile with insignificant clearances between the adjacent- rollers. This ensures an axial drawing of metal by all-round radial compres- sion, and improves the plastic properties of the metal, permit-tIrIg a single pass rolling of drills from P18 (R18) high-s-peed steel. 0 - Card 1/3 S/1 22./61/000/0 1 -1,1002 /-:)C,6 A new I o-r- 7et hod D2211ID30-i. L- = i + mm b t 2.2 V-' " - h or- ,ld,here 1is the length of shank, and I is the lenEi,-, o e w z W .i n r t of lu-!,e drill- At the start of the workin~-~ part there -a aefeeL i,ve portli-on uhlit must be removed and wilich amount-s to of the drill T'ne metal ha!~ a tenden.-2y to wid-4:-h ex~,,~nsioota rollim, and U~herefore, the diameter of the, lands exceeo6 11~hat oi the shank- by O~2 to 0.35 mm which is rem-oved by -relim-inary, The segments are made Jn X12 (Ia-,12Y,' steel, icenterless !srindilng, J- 11 or of other marks. Their hardness is HRC 58-60, and are machined on a relieving lathe. The life of senments is usually ~5000-7000 drills. afuer which they must be reground. The metallogra~cruc tests of drills rejealed the hiGh quality of roiling without de- fects and indicated a sorbitic t.~7,e o_`7 -Pearllte w--*Izh uni-lF'or- d4_1 but4t.on of carbides. There is no decarburation, The uroces--Z-en- sures a 30i;'~ saving of higl7i-speed s-ueel, and a 15-'L old redupt, ion of labor com-cared to iq-illin-. Card 5/3 0 0 0 0 0 9, Nq oil ) i1$ to siollujIMIFIL1111119 0 A$ At 0:11 K-L-L-L-A_JK_1-_Q I ..i-A 1 0 C1.1- so A I A too ..0 .1. Fooc I Ill IAfto poottelli two~o 00 The develimpmeat of the Cavicaptles 4W the cherMW ale - 00 snotat. V. J_Spkayu awl N. 1. 111"ov. Vipekhs Khios. 6, t7W-3(Z fiXII); C". Zewtr~ 19M, U, 643.-A we-4-n- wn of the We* of the clement Irian antiquity to the at t prewul timeissi"u which issuitablefortsw in in'tructioll in secondary schools. Several definitions of the tt-im by twitafern autbows are sivrn and the VAIVIlk, Alki 1~h,tviw of isoxop" tit elenvornts explatint-d. ficatkin (if the atums are differentiateil: (1) aceording to the w. dinwriskins (system of "inowlidrs" according to Ale* 0* a Monalry), (2) according to the at. masses (system of lonides" accardino to A-non, and t3) according to the 0 +rm. and radictactive pvt4lertics. M. G. Nftx)fe ass 41-11.1 117ALIIIrIIAL 1.1111611011 C1.1111111AMI Tic., Sir-NIL'. i4lova If City as( Z;90 x0e :see I Ally Ir* 0 @$Lill Ow 0.1 19, oak Ah u a AV 10 &,1; A, it t; IN 0 910 0 0 0 WO 0 0 0 0 0 0 0 0 010 st 0 :::::0000040 WF 4 1 4 1 it U Ij W 11 16 11 A. ~L_Jl _A_JL_I_A_L .8 it f 4 A 040114% , a JIMUMMISUNip it a ij 4 _l_.I_AA k a j k 0. 1 1 I I . .- 1,40CF1111 Aho I'll"I.Iql Products of decomposition of sodium paratuagetate an melting. ViLl I J. Gen. Chr-, - W. S. S. R. i 1lil a StAi-75(in V ;l N lee l . . g a piratu"R'I'll" W-.1, PrcPd. fmm tuit%stic acid all([ Naolt. 'Ajialvsj, ,f III, 00 product showed it to be Na..W130'. which oil delly-dration and melting titcotill's. hill, and ' With 110, Na3%% Ah tracts to Ilive Madf-r%ky 00 00 [ LIIIIII&II641 -7- 'Dom, -------------- T_ 4-C OnAll*-c r 'V U N AT 00 is !ZA eAnel 10 9 0 00 * 6 0 0 0 0 0 0 0-000 94 IALJI a W 0 #1 0' no V 01*8A 0 0 0 0 0 0 a 0 0 0 00 0 0 900 -00 00 ts '00 Bee *e 0 0 0 0 0 0 0 6 0 it 11 R I JD 11 V u L, w 1, o a E 0 1 11 L t i. it I L 11 AA W U.. S t *0 A Stuay 01 lithium isUP01013114s"te, Vlkt- I- - A '-** I M. kult,hiiv And 1, 1. Tikhornitor. J. Cen, CkePM. U. S~ S. R.) S. 1527-M(in I'much, I-'"U MWO.- A I: tu,lv uu~ firadcof the syqrm Lj,WO,-%VO, by hydrolyt- _00 ttlit all cold Ilp, fitllo%ed NO liv clivrok-al analv-i,of the tMo, I,, ;oW by 111,U11% of 1-.h., Me ge- : -60 ,It, I'v N-111 wele sit %'..I Is% flit- . .00 -11.1 ~Iat% ifteiv I-xi%tN only %ofir 1,i 1-tong-141r, L"U"o" 1411%,hall"ll mid welling M-1 A- 31111 l%UkA-tn1lK1tAt". Oki mid,tgo the following rctictiom: LsitV.41o4 2W0,111141 1.11.wot)o - 51.f,W,O, +- On neltinx. 00 h,Wj(h hrrALs up, but only Itattially, into U,IVO, and WO, (In livilrari"ll LOVA react% will% 11:0 a% follows: ' =00 + 3111.0 '-'Li,%% O. + S. L. Aladorsky =00 * 0 0 : .00 00 lee '00 90 00 00 L -EVALL MICAL LiTfW.TL9f CLAWFICAT CK Os t t- 1 00 3 1 10, S'. 4I,,, i kes 00 It @)till -za '14, it! lee r l L it 15;~ ~ w I Iff Id a Ai I v IM if ; If it St K it 1, 0 0 0 0 0 0 g 40 0 0 OVT448 * 0 o 0 0- 0 0 0 so no- =Jsll !~SA u it a one f L I A 9 ~40 I TI ALA 14 f.( W 410 -.40 ........... . '00 helyr-T-r"S R 00 kv%tat, '4 w .v Ititv obtaitted I-v Ah-winr a ~klm cmttg. N .10"- 11w;mhvJ alt to ~tatul fiq -v,-tal %v,L--r -1k m 11,11 at "'l, t. 1.".I t.uf~ "I 41t, I-Off Ij 00 0 0 09 .00 0 0 00 coo so Zoo 00 age 00 ~zo* 00 woo '001 zoo 00 00 480 00 it ft N 11 rcT.- V W-4Y 7'DON 0 a 0 0 00 0 0 o: : 01 0 0 0 a 0 0 00 0 * G.A -SL me W v .-W of 0* a 0 00 *Otto** Ca 0 0 0 a 0 6 0 0 0 st 0 6 111 'i it 0 A 41 I I AA N U W It 0 00 0o 00 Reduction 01 Ud"m CMUSISUCIFIR with hydrogen. VilLt. 00 K-chalov and N. 1. ,,Itxov. J, (;rv . R') 4. pSM? X On H zxlj~j'. is1k.41 f " -00 .4 I-11h.0 .. I In. 1. ~t. - . it , 6'. f. ;n I It- WIj, -00 W twain. At 4L.4- And 1, qn.11t, .1 Ingl 00 0. (111 isclutntrd I0 A I'lixt. of land lower W vude, -0 IS tat SIx)-7fW and iscOl"Pletely reduced to W at I(oj The reduction of LiAVA, (both Pam and incta) proceeds in three stages: at 400-"' a mixt. of 11 and lower %V 61016 oxides is olitaincd, which with further elevation of the temn. L% reduced first to I and then to W. J. L. =00 400 00 3 00 7 roe '3 71 ze 0 00 0 It 00 to 0 of t! 00 1 coo :, zoo 1: die 00 I . S L ETALt.1P.(;1CAL 1.1111PAT4RE CLAS51FICAtIC~ r' z *0 i ire 0 UC 's. - O o 0" '0' 403 1 (1, CY Ir 'V M OF It 01 If Pt IT I or 00 0 0 00 1 0 n An I a .w o i n I is 0 0 111 0 0 0 00 00 000 im s A a 3 1 000 0 * O 0 o o 0 0 We O's 0 to 0 e It 0 J/ 000 00 0;0 o o * o00 0 ~ ~ l a 0 10 0 ** V W-4- is # & , M JU 1) is 11 :7 .1 r c 1, ti A 6 r U 0 1 V V V I AA td U LID ti it The reaction of columblum pentoxid., with h -00 and N. A. PreubmihenAll. chloride. Ckem. (U. S- R.) 10, M5-M(l940i.-EvaPo. t f -00 4X in the IlCt sirram begins at 4(W)l and proM-dj 4 of O -00 0 Is j Therractionis: CIhCX + 6IICI -00 .10K)Ct. + VIA The equil. can-it, Is of the order of 00 at 0XV. ne vquil, I% easily shifted by varying Thettluil,ft(ablialicilAt high Irrnp. 0C) l f di h o f 0 f fi 1 ly. fitt o e ( r ct it t , 411(t., 1111(ing ox nK, dmlysk and the productiol hydrolY41-4 WP. In the folli,wing t M)* CbOkCl WO-4W CNO tUl )WlQW 1 nee o - ~: .1 a .. a :Dxl* "white subliniair" frol"dal di~pe"i-n) of the ,VMpn. CbkN 67, 1ICI 14, HO t4, CbOCI. 5% and PtIltuibly some CbOCl. The Ist stage of hydrolysi-i Iabove ;K%)*) consists in the formation of Ch(NCI, an.] Cbsob forms as the rrsult of side reaction. Below :AW, ~~j goo 00 the hydrolyiis W CbOCI, proceeds directly to Cb,,().. (' wt of h t b t 211 f Ct (b uw ~ a ou . The hydrate o h a y % % o%Wc) IIC1 at rowt temp. The ahsintion deert-uw-k with an imtrav a( torip. and alw)s-e MAI no almirpium 4 IICI was ofis"ved. This is expLained by Ab~xpiitm e 1-f IICI with colloidal .1141wr-d CbC4. r"t- CWh r-O 0 d.- not al".Wh MI. A. A. Podgivnr Off-.101! i- J) 01 I' 1 t O 4 1 " t f 0 IN 0 0 4 1. t I l it it x A 11 i L 4 1 1 0 0 0 0 0 a Is 313 0 00 00 0 0 0 a 6 0 0 Is 0 0 0 goo* 0 0 0 go 0 0 0 0; lam I Z j 4 0 ;:j 04 0 .201 - - - - 04 06 0 0 6 0 0 0 0 0 0 0 0 0 * 0 00 i i 04 1 1 1 1 1 U " 11 11 4 X , V J425 Ust Milo at au 614 ZO ' 1 . . 1 . a I --&_I I V!EAAPAkt-, 0110ces"s .Dr. The reactions of columbium, and its compounds with chlorine and hydrr tworide. vilit. 1. Spi"r anti N. A. lIrrobrarb. if. J. Gen. Cke". (U. 9-5: 10. 78t-VS(IRO); cf. C. .4. 34. 7t7l'.-Adthil. cipti. data show that Cb oxides been to react with MCI at 3(X"00* and with Cl at 35(~-700*. Sletallic Cb powder reects * and 300% more energetically with Cl than with MCI at 19D resp. The reaction of Cb powder with Cl fortocid CbClt and that of CbA and Cb(N gave CbOCI,. In the pres. ence of 305, charcoal the 2 oxides react with Cl and MCI at 4(-X)' to give a mixt. of CbCI, and Cb0CIs. Nacbo.re- acts with Cl and MCI in 2 stages with the decompri. to SaCl and CbA% and the farmatiim of CbCl& at higher temp. (about 1000"). Cli powder with IICI gives CbCI, ON and CbCl& with the liberation of H. ChO, rvacts witki HCI similarly to CbA% to give CbOC4 and its docornpn. Pr(Aucts. Chas. Diane - &10-$L& ACTALLURSICAL LITINATURe CLASSWICATION 11:1., 14-otto -1 1434W "it Get, Get b As .1 ,, , ; .1 K' Is 0 sooefoo9ooesooooooooooosoooooooooooosooooooo COO goo 'too ;;0o too see moo ' so 00 ts 130.1 woo I Is SU131 Met 1341111 Get 049 IS1 0 is W I IF of 0 0 0 0 0 & SPIIISY141-7 V.I., PMFPI3PAZIh~',:)KIY, N.A. "ChlorinatL(ni of Nlobitun and Itti CompoIndn" Zhur. Obahch., Mini. IC No. 9, 19140. Lab. cf Inorganic Chemistry, Moscow State Pedagogical Inst. imeni X. Libkhokht. rcd. 1 Nov.'39. Report U-1627, 11 Jan. 52 0 0 0 0 0 0 A I It L a _L__L_s_ P Q 4 A T If V, w Lt o* J! Normal Ik tfsas"s". V. I s d I'Sll~ - 117t~ IT32 (11144) 7 M , , _ wM mak. 6elf. f- - ' 111WIlK IfCtMI b Ii t ItAtt Wall t j s - e U Y (f~. j *UMMMy)- W j "Sljx III She by- and JW(h 1k(OII) o . # equ. I ht ttin l ( k 00 e Or ,, it m 4rated fo;ws, bafte the sugw-Os %tand for4IIII-MIdaysat room. temp., then boiling hic I hl The viwous prodect an PfOkmXW Standing Ov" PA)b AnMyted a. 11tw0t.21110): lite twifinal PPt. hIefurt drying poswo,hr% the cticnim. 1;eWO,.3IiO. The mthstance i, I t hysrtw-tbpk,, It 6 insal, tit watet and u-As*l -wit, %4v~w- "! ' [ell 1k.114tit ()n liffOhICI t b CC[ i 0 ) 0* WMjrjjV . ti . S Mit, I f,1 (I , 9 . With waterI the IMAn. shoWs WO# isAll; this hygis.4"t'. 1, t 125" ficatitt l i 00 . 01 . ave a n an awav v IM-ricrat,41 by heating " cau~ *vnipIrle dehydration and i1mmitpis. "I L34) 3W f f fl 0o on o st'j. o :,It. th-4) an,[ WOO. lflt~ro' 1w.k. Be t1lugst.tv. strInI l i 44 id t d N Wo , s n% e ~. a A' s y . Y 00 (I. oe .09 we 41 -00 A%- Ski -CIALLURGOC.L kittRAT(lef CLASSIFICArSO11 CIO We* r" -u '11- 1. If , n ~~ I I I :%P IF IF VI a .1 J If 1-111) IS I I Va 0 00 111 oie * 0 0 000 00 0 0 *1* *Go** e 0 0 0 see ~*- III - oLe I *0 * 0 _O* a 4 0 * 0 0 0 0 0 0 0 o w 0 0 0 Of 0 * 0 0 W WWWWWWW: t I f 79 a- i a it If N I Is I- 4A ~10 k# _WW P"%US AIND 01IM4141 1%0(4 00 1 Tht nomal lumstat" of ribldluni'and of "*Adam' V 'col' loss and sirmwly hy RbjWO, silao S itvmoscow state Univ.). J. L;-' C"W-?L"i- 17'. Is 817 at 00 ;A "Ya IWY 170, 86.6%. on 1P SA. 20 "- cryvtn. how solo., RblOsciontairts water iftbtly abo" 00 the Ample tungstat" by 1"Xion of WO. witra. Trattal "flawlate- fail"t to give pure products, obe alkali 0-5 160 about IA of which is loat an standing ovvr PA; -06 0 * a. , wills to more 140 1% loo am heathur'. the UP Ccantent of (ar"bly hatrtlol dlmuh-11. ain't b)t w"Y a 0 t fit. CoOlk1h, r-art"twmilitit apprin .1,121100. J. allaill'to r1rhAlute WIIto 4111ral" a* rlkr ionattes with 04XV04 Wy Just on *161141101 over I- y'4 sual am hvAtlnv~ Aftro Moo was un,uvva-a(u 1. o- ins t- rev ei %aibillty Of the let" 1011- crystn. by tvapu. at 100-1:X1 , the lljO contents of tx)th Most successful was the double exchange of the ch e2 RbjWOj and "WOt are less than 0.3%' bencep the with Ag.W'O, (prepd. by ppta. of AM), with NjkWO 4tunWates forns no stable hydrates. On mlittow a stals- and drying the washed Ept. at 100,-l 10% preferably by cifttly concd. sarin. (down to 0.74 j./ml. RbWO. or moo fusion at 4(0-W)" wit a 2U-25% ex"ss at A&WO.. 0.48 g./ml_cs' Oj with RtOH, a &a". Into 2 liquid 00.3 The product is kept in the dark over PaOs WW alkali. layers takes place, the conen. of the tungstatt rising In the oso 0 crushed rapidly and twice leached with water (each time, low" -sk. layer " Its vol. decreasing; this " -** *go St) mi. W 6 S. initial chkaide) under exclusim of COs- egact Vajoa obsermd with K*WO* bet is absent7l 0013 the lot leseblat is done in the cold, 10-12 hfs.; The i;'J'boath NBWO# sad U#WO#. RNWO, M. ON" -12"; at boiling fur 10-15 min. The ykW Is 90-0% of the C4hWO, m. OW -i- 2*; the Ist figure Is& low I I, - er int a" *0 U theory. the tomes occurring by stomwptice cof poet of the M%& as the sample contained about 6.6% K*WO,. moo mobs. by the AcCl ppt. Analysis confirmist the siliciple: Temp. affed, m cooling, corres I CIO 00 X pond a polym bous tarmulas RNW04 WA CkWO4- RqP"ttd fuskal w", tressitkins, wm found for RNWO# at 517-51560.7= A%&WO, did m change the catupats. The comapdo. we 3WO; for "WO. at 5W* mW W-9-= Btonwas cmpn. is observed for RthWO4 mt about 900'. 1- CftWOs go at NO-10OD"; at 1200", d-pa. accompaided by was voktaintinor af the anWi metal oxide, is marked. N. Tboas moo a Ale.1ts a(VALLUVGICAL Lnl*ATWI[ CLAISSIPOCAT" VIVO SITO 4114111 OK a" M oN v4#1 4 2.9 9 AR A S 0 U is AV Is 0 to to W It a It go sees 0 0 0 00 f, S see* 00091 Thenrud stability and r3ladlity of normal alkali metal Mate*. I Pkill"A.411.1 V. 1. Millititit. Illff, 1111u). .11,lkthoi Akio", Wiwi. owito it, imi x 4~ No holit 14 wt. woo fosiml f*1 lWallew of 1104)" a hF*. ilreli"I at 00) OW PON, (VONIIA4 In the JAMWI lifties (I# ) I Lh 4). VV MW 0,41IJ MIAL(h 11464 OAA' Kom If 11 soul 11.12. 20 h W(M awl 1,2Y, C*.VAJ6 0.30 mall (00. "I the mtoo mUr. The oweapostding let. kwas (vainples .I.2AL(I..%I 1.) 11" 2 htfl.' lWaIllid lot JINX)". Wftf I III, (1.A2. 11114ri thil In "It all .11ralls jWj 1.1 ~tublj. 2.S0. O'N' .1.1al. tkI *_'O~".' Ill. "'cle"Ic of the air stream velocity to o.4 reduce. .be I'Al' possibly as a IM19 Of Cowing. Lin-WIP". oil (2-32 his.') beating t 12W' detd b analysis of the ruWue.atmmutedtoOl.0.21.*O,O.l~7l~..resp.; hence losses by simple volatilization, detcl, It the same cipts.. V.88, 0.777, 1.70. 2.#V 6.94%. At the same temp., in Ii SIMAM Of 11,0 Tll~~ "i g-f .. in S tUtXLS]( '2NJ tntn. them., the loss of wt. was 17.522, 3.69. 11.76, 40.44. W.85%/hr.. the decompn. 4.78, 0.31, 0, 1), 0%/hr.. hence the Im due to simple vvistilitation, 10.84. 3,34, 11,76,41).44,90M%/br. 'nw 3 sulfates, KISO., KbbSch, and CsS04. whicb have the highest mithing temps., u6o have the higbest volatilities; the mol. volatilities at IWO' are in the ratio 1: 1.4:2.1. i.e. markedly different. despite the great closeness of the melting temps. (1074. 1074. .nd 1019'). Consequently, volatility is dctd. tsot so nitich by the ionic banding in the solid crystal, but by the changes of bonding that take place after fusion; stronger lionding in the wild state seems to give fist to weaker tk)luting In the liquid state. The Increase of volatility from Na to Rb Is attributed to polarization of the cation by the 0 atoms of the 80a- anion and corresponding shift from ionic to polar bond, which effect increases from N*a to Rb, but plays no role in the cose of the very small Li. The high volatility, mW Julie welting temp., of LIJ9" is dtm! to the polarizing action of Ll an the 3%-- anion. re- sulting in a decresse of the look cbwwter of the bond. Of the S wilates, Na.SO. ban vide fly the strofigest ionic-bmW chluracter in the fond mate. N. Tbas r, 0 Ressar4 bft On dwad dabWty an4 walatiRty of dw, normal wagon 40 aw Sam dow". vly. 1. sr!sylt, and V. 1. Slimisk (MacowlUale Unly.). U.S.S.R. It. -No. 11). aall-40040)(PnIllih tranAi- flou).-Scc C.A. 44,417c. F. 11 C. two$%$" 01 Is. V Sao saftlo. V I v4W1%yu (Moscow State Univ.), Zkor, mj1km'K4iW- U. CWKClirm.) 20, W-40m)). - hrousling W" a# wt. flist to VV&W. 8*1 pastial lketmnpn~ is otwtvrd at Ow folloolist; trumps.. Lh%'(A Mul. Ndj- Wo. law% KSWO. RAW, RbIA*O. (MO. C24tv" um . to the dweams.. the a" "Wital Uzi& is Wlit cc. in 0 hn., at 1300'. the depm of dtmnpn. 6. in tits above mdw. LU, 0.30. dAd. 2.35. 3.34%. The thermal in. stability of dw tuaptaics U( LI and Na Is linked with the. dUct of The instability of tung- tatnal K. Rb. stmi Cs Istictif. by the w&m-tive poLuiAing ect of tk* 0 itons In WO. oil the alkali mclal lausond N increams Witis Idert"fix kmk- Mitts and jxAmt1sability ul dw cations front K to Cs. The raiv ul rympit. varl"' in the same onler as the depre of docuinpis. X. Thun Tbw=d obbfty md IW$ftl of mmd fteplair" of the on" dom$W&, V14r ., 16,,%kwo (M. V. Lwnws" StAft VOW. WOKOW). , tM. C". (f.S.S.R, n, 570- WJ(IPWXRne. tra"tbm). See C.A. 4M. S243d. R. M. S. 4- A_~ T~: 405 ~-~inary's~ptexrt jUh2W+-.WOi. :j AND VM* KULPSHOV. Zhur. Fi_- Kkint., 24,---Tjjyr:n.,t2qT-rflrob); j, 'F .1 b.11r., 4 151 2845f (1955).-The binary ?,ystcru JIbjWO,-WOj Was Investigated by the vimial-polythermal method in 5 jl~ steps up to 20 Itiol. L'/(_WO, 11114 ilt VfL) rwp~ from 20.to 85%; f .101M the Ille tvil-luctal"ki 1111pro, i an, C: 1110tilig poill, of'Wo" tilt, WOJ Volatility, Introduck I appremil ~cjablc error; Rb.-WO, iias prepared by it Inethttli previously dc-~ of 059", suibed, but its melting pobit.Av--ts'05'VC. inst % WO, rose; liqiii(Itiq beyond the eutfvtic af 5G3' Nvith.39 mot -'and 1033o cuntilluous y with~a slight itific-ptiolm at (180% 8d_ ycind'eaW correspo nding;to,51 138~ and 84 Mot.' Woj~ Be lu ection a diffuent cry4allitte form appeared in the nielt- -this 7 Suggests- tit e; coljlpauild~ -RbIWIPI, RbIW,O, and Rb~ hexa. J tungstate Ivith approximate incong I ruent me fjug* pwol~ts orusl MS'I' and 1646 It is:notcd that the tendency W Iona lilgher. dity frow LI tit Rb and that the st~biiky tile I Itung of 'M 5tates &6feas6- tilis is ascribed tc; It e dL -creisiT g lects of ions With *iilc!r c:u iugjac~ L USBR/Nuclear Physics - Isotopes 21 Ap,r,50 Periodic Table "Periodicity of Types of Predominant Isotopes of Ele- ments," V. I. Spitsyn, Corr Mem, Acad Sci USSR, Inst Phys Chem, Acad Sci USSR "Dok Ak Nauk SSSR" Vol LXXI,*No 6, PP 1053-1056 Distribution of predominant isotopes of elements ac- cording to types of atoms, e.g., even atoms (4n, 4n+ 2) and odd atoms (4n+ 1, 4n+ 3). Graphs shov atomic type according to mass as function of atomic number, for main and secondary groups. Notes definite regu- larities. Submitted 15 Feb 50. 175T68 V. I. PA 1165T48 USSR/Nuclear Pbysics - Nucleus 1 Hay 50 Neutrons "Problem of the Ratio of the Number of Neutrons and Protons in Atomic Nuclei n V. 1. Spitsyn, Corr Mem, Acad Sci USSR, Inst of Phys Chem, Acad Sci USSR "Dok Ak Nauk SSSR" Vol LXXII, No 1, pp 41-44 Considers ratio N.INp as function of atomic num- ber Z for odd and even elements and predominant sotopes. Gives graph, table, and formulas of Np vs Z. Submitted 15 Feb 50. 0 Aft 165T48 spi'rSYN, Bri Spitsyn, I.'and Kyleshov, I. M. Investigation of the binary system Rb 2 WO 4 -WO 3* Viet. Page 1197. The M. V. Lomonosov Moscow State University February 14, 1950. SO: Journal of Physical Chemistry, Vol. 74, No. 10. October 1950. USSR/Chemistry Titanium Compounds' ~an/ipeb 51,; "Investigation of Phosphates. of Titanium," Vikt. 1. Spitayn, Ye. A. Ippolitova.9 Lab Inorg Chem, Moscow Order of Lenin State U imeni M. V. Lomonosov "Zhur Analit Khim." Vol VI, No 1, PP 5-14 Studied interaction of titanyl saIt soln with phos- phates under'various conditions. "Titanium phos- phate" ppt, dried. at room temp, is 2T102"P205*H20 or (TiO)HPO4-2.5H2O-in compn. Compn when hydro.-,. lyzed: in water approx 3TiO2'P2O5'6H20; i In alk 177T7 USSR/Chemistry -, Titanium Compound Jan/F6b 51 (Coutd) soln a sharply reduced P205 content. Detd optim- conditions for sepn of titanyl phosphate. Coagula- tion of titanic acid by phosphate ions and their chemosorption by titanic acid gel occurs. 177T7 COMOUMw t=ty OfL-Nor=i"~'MdlTbftteo-~'of,Alkol-I Ellemeits' LV:Lkt,. I. Spitsyn, I. X. Kuleshov, Lap, inorW77 OJ H C*Ipi Moscow ~ State U. '.0 "bow Obshch.Kh&'- Vol XXI, No 2, pp,401-4(% Normal moly~dates and wolf remates of alkali metals- evapd - considerably-- and decoupd with sepa dt,alkali oxides Iwhen heated at !1,2000. Rate of-Aecompn of all compd and rate of evapn or, volframates increased for metals -in order Na, Li, K, Rb, Cs; rate of evapn mo!7b"tes in 17&2.1 WSR/Chemistry Molybdenum- and. Wolfram Feb 51 Compounds'.(Contd) order Li to-Co. Thermal instability of Li 'and Ba molybdates attributed. to growth of contra- polarization processes In compd;-Instability and evapn of K, Rb, Cs molybdates explained,by polarizing action of o-- ions rrom,not fully integrated anions. ,4 17&21 E- La C~9 Naraw mislybduss at rabidim and of evitium. c1 1. M. Kulmhov (1%10~cow S atr Inv.). t t1hyd. RbiMoO~ vva-% 1wetmi. by futiou of %Io()j (porifitil a.% I the prftv(llng silmr.) And RthC(h. Anhyvf. C-,Nfoo. w.4- wepl. (0o acmunt 44 the vollatilitr Of CMCO,) ISY IlkliOn if Astlitnot (we preceding mbstr.) w th CsCI. The A&MoO, was firm fused. then 2 CsCt added slowly over2l)-414) min,. ml fhe cooled turit was leached with litc) fit cite cLuk for 3 1 lim. and filter Coulpletr flip stwin. W~1' dt-1-mittA and rv;Glftf, un a water Wth. Me protlucc~, KI.,NIoO. anti Cs.-MuO,, are white, and strously hysroowir. I'lle -0111NIMCS at 18' are. resp., 67-M and 1;7.fr C, :Itx? jr. ,ttln. (6.4 and 4,8 molesA.), the imps. 92V and it-' j", reip. Ititerplanar distancrit of KeMoO.. Rb,,%IoO,. and 00loo,. .,re .cry close. Tbernmigrants show eudothrruml pol -v. morphic transillotim, In RbMoOt, at 271). 287, mid 1:15", -kild In CS.Moo.. at 400. 47d, and SIO". N. Thun C Ei Molybdate a Aug 51.' 'JSSR .%try, - Rb and "Thermal P~nal~;sis_of the Sy.-~:tem K2MC'04-7MPO,,, ind VAL 1. b of inart ~'bem, Moscow Order of -enzin IJ Jxu,,ni 11, .V. Lomzonosov "Zhur Obshch E-Iiim" Vol XXI' NO 8, pp 1365-13711 Contrary to latest literaturei data, di-) tri~-j -zonra- and unstable hexa- and octo-inolybdates of K and Rb exist in these systems. Liquid-Lis curves of Rb and K' systems are sizzilar, There is no dimolybdate in Cs system, but same other compti-t; az in Rb system. Deec-rlbes cryst form and notes some reKalarltic.F- 'r. cip of acid mc-lybdates. ;-" 184- trosll/Cbemistry .. Rb and Cs Molybdates Aug 51 (Contd) Found exothermic effect. at 370 -for Cs molybdates. Ass=es existence of reversible conversion in solid phtases in ELcid nolZ~bdate systems. MR/Chembg~ "Investigation of Isopolymolybdates of, Alkali: Elements by the Hydration Method," Vikt. 1. Opitsyn, 1. M. Kuleshov, Lab Iuorg Chem, Moscow hate U imeni m. V. Lomonosov .Zhur Obahch Khim!' Vol XXI, No 9. pp 1549-1561.''~-, 'Investigated melts of acid molybdates of Na, 14p, Ki.,..Rb, Cs of compns f ram 1*20 - 2MoO 0 3:t0 Me2 5MoO3, f ound that each metal f orms only 1 stbar ble . sopolymolybdate. Li, Na f orm dimoly:bdates; X,,Rb, Cs - tetramolybdates. Even stable, compds decomp slightly into normal molybdate, and M003, -1932311 USS IR/Chemistry Molybdenum Set.. 51,', (Contd) or. ..Aydration of isopolymolybdates with -H20 (cold Li, Na, boiling for K, Rb, CS conpds) converts them to sol molybdates. Indicates most expediivnt~ ,:method for prepn ~of stable isopolymolybdates by 'hydration method. -191T33 tr SPITSYN, Viki I. lay b y the metw Qdl Kulesbov,'(M- X, one" Ges. - 4--mm fl I a.1K. a&, &dV&-& &=a tiGR); ZhUr. ObSkW KUM. 21, 1 1 1 * d. C.A.~ 46, 9006h.-The m ip I . omarring at r=m temp. In wefts of acid malybdates c# the -1bull _ 6W. by- Chemicea Abst- anal)-is of succmdve water wasbes- On.metbad depends- on differenm in ratts of hydrstim R Ow ccenpownts c4 the: Vol. 49 NO - melts. The melts wen prepd. by hi4* it caked. amt. of MoO~ with the resp. carbowta (or with the normal malyb- Feb- 25P 1954 date irr the casc of Cx). In U and Na uwlyb&tes there s~njc Chemistry r J %vere found for M*O:UoGa - 1:2 M*116A and - of no g M,NfoO. and MoOt; for MeO:MoOs - 1.3. 1.4. and 1: 5 them were fotmd MXqA and McGe. In K, Rb, and Cs molybdates for M.O:UoO. - 1:2 and 1:3 tbere, were found M,MoO, and M.Mo.(6,, for M*O*.Mo(h - 1:4 and 1:5. M.-MoiOn, bisMoO,, and Mo0j. The isupolyzaalybdates of diffemnt compn. that an detft-6ed by tbermal analysis clurin& the solid1fication of molten mbft. do not exist at ordinary temps. The rmut convenient procedum for prepal the dimolybdates of LI aW Na and the tetramolybdates a( K, Rb, and Cs by the bydratiou method is outlined. SPITSYN) Vikt. I. Chemical Abst- Vol- 48 No. 4 Feb. 25, 1954 Inorganic ChemiatrY arjof" e dates of the &Uc&H elements. U L, K V%f, V. Lomonosov Gen. I-Rem. U.6_3.77771, 1717-=(1951)(Engi. tmnsilation); Zhur. Obshrhti Khim. 21i 1564-70(1951); cf. C.A. 45, 5553i. 555-1f.-Calcining melts of the acid molybdates at 1000 and 1200* results in an appreciable loss of MoOl and in the evapti. of certain molybdates. At ratios of N[oO,: N110 in the melt greater than 3:1 practically nothing but Moo, is evapd. When MiO.516foOt melts are heated to const. wt. at 10006, they yield the following residues' N&40_10,~ Cj~U;Pj& o&.,, v~~d Cs2Mo30w. The dimolyhdates of-Li and Na, and the trl- molybdates of K, Rb, and Cs are the most stable at tOf)O- 1200*. Stability relationships are related to the polarizing effects of the metal i0jis; the lower the polarizing effect the; moTe complex the anion of the polymol ,vljdatc that can be stably asiocd. with it. Bernard M. ZetTrrt-,. V.I,, prof.j red.; IAPITSKIY, A.V., red.; aRLOVA, N.S., tekhn.red. [Radiochemistry; collected worlts) Radlokhimiia; sbornik ral,ot. Pod red. V.I.Spitayna. Koskva. 1952. 358 P. (MMA 1-1~: 6) 1. Moscow. Univeraitat. 2. Chlen-korrespondent AN SSSR (for sp#4n) (Radiochemistry) 8PITSY14, V. I., SHGSTAX~ V , 1. ~ and I&YEROV, M, A. "Investigation of the Volatility of "hlorides of Alkali Metals at High Temperature," Lab. of Inorg. Chem., Moscow State U., Zhur. Obahch. KUM... !a No.5, pp 758-765, 1952 The temp, condtns of the beginning of visible evaporation of chlorides of alkaline elements in gaseous media (air, hydrogen chlorlde,water vapor) were ttudied. In air, volatilization starts at the following temp: LiCl 5500, NaCl 75000 KC1 65001 RbC1 6500, CsCl 5500. The volatilization temps in a flov of hydrogen chlorideor water vapor were the same within a gange of = 500. The above compda become visibly volatile at temps 50 to 1220 lower than their malting points. Vaporization proceeds considerably faspr in a stream of water vapor than under heating in air or in hydrogen chloride. At the temps of the acpt (550-8000) this process is not accompanied by hydrolysis. 258T15 SPITsvi -1. Chemical Abst. vol- 46 No. 6 :;;ToiwrYt-Yf alkaff-i 11 ' ' tomp fures.. movi twow Mar. 25, 1954 eipt. U. '.V. 27 General and Physical Chemistry (H1191- trn"5Iation).---,SM CA. 47-N*3067h. USSR/Chemistry Alkali Metals "Investiiation of the Pyrosulfates of Alkali Metals," V. I. Spitsyn, M. A. Meyerov, Iab of Inorg Chem, Moscow State U Imeni M. V. Lomonosov "Zhur Obshch Khime' Vol XXII, No 6, PP 905-912 The pyrosulfates of all alkali metals were prepd and characterized. 218T12 SPITSYNp VIXT. I. 1vilkali elameMs. t-Vikt. 1. Snitivii ;T3DnMY W V. Lo. .77 Mex.. U_~..xjr. tMaslation); Zkur. Ob;kW Kkini., 22. - 901-wXIOM:_ The -Ikall mital add suffates wem pkerA.- by impt. "IRS. of the p)rosuffatts (cf. following abstr.) over PA. Tlfe _ystalsobtained were anhyd. The rn.ps. were- .404*~0.5,,- 186, 216,285'and 110* for the Wts.of Ll.to Ctiresp.'- Slow - 'Chemical AbBt. decompa. began'at 90-100, 14D-150, 100-170, 170-2M and 150-180*,for the 3alts of Li to Cs, res In all mie-i the Vol. 48 No. 9 decompa. prodticts vie. the coffespoudF;g pyiOWIMies In yields of 982-100%. -The salts ~,ould be tuelted r 'Idly ~Jay 110v 19"',4 with no petviptlbl~ deempn. . The temilts ke- dii~ Chemistry from the standpoint of the I~olaoonj actidn;- and. poiskis. Incirganic R. E-_T_riM_W4j~ Chemical Abst. Vol; 1+8 No. 6 ~Lnr. 25, 1954 General and Physical Chemistry !,,Effect of garcous inodia on the evaporat~pn rate of alkali chlorides-- Vikt. I-Spitsyn ant) 11, L-Shovak 'Mair V"l-, Moscow;. Laur. Uh5achel Khtm. JLC~--il: J. (,tn. (.4em. I _.*)_').K_ZZ. I Expts. were made in an clec. furnace at const- tetrip. of 8(W~ Controlled vols. of air, water vapor, and gaseous Nfi~ were passed over Pt Wats filled with.alkali chlorides. Gascou.. .CO; and 110 were used off CsO orily, The rate 0 c I wo.,; ile-d. by differt-tice in wts. at standard tinic interv I The reboltR nhow: (1) At con.5t, temp. of SM and gms floy (OA 1. pvr inin. N.T.11.) the rate of evilpti. increascs In thl order Li, K, Rb, Cs, nnd Nit. (2) At const, flow Mte of thl gases the rate of evapit. increases in proportion to them polariq-01thegisused. (3) The effect of the gas polarity isl grralt:si ,i, MCI and Cs, the smallest on NaCt. Evapti. of LiCl iii , liter vultut is twice that in the air.' (4) At low gas flow tal 1 (02 1. per inin. and less) the rates of main id q)tical for all gases. Ist. 0. H-.-.. SPITSYN~ Vikt 1, Chemical Abst. Volatlilty of alkali a from their aqueous solutions. La yi4- Ij V, LonlongaRv Ejj;jMQ an Vol- 48 No- 6 W, el Kbim. 22, wii-3; J. Gett. Chem. U.S~S.R. 22, 1117-18(1952) ~Detns. made on Mar. 25, 1954 0. !N soins. of MCI. KCI, RbCi, and CsCl showed no vola- General and PhYsical ChemistrY tility of chlorides from the aq. soins. M. 0. Holowaty 14TAt I. SpI-L,SYN ) ,/The soljktjjltK Off 4PA4WA~UL Vikt, I. $Isil-lyll 0 01110 MY ( 2 . . -N1 J arn CTV7Ifj Tin- -, . , I tiOn); Zhily, Obyhchef Khfin. 22, 1278-81(1952).-The soly. in waterafnartual Camolybdateivasstudied over the tmp. range of Colorimetric detn. oi the Mo content and detri. by the method of evapn. of satd. solus. of Ca chemical Abst- niolybdate gave resulb in close agreement. The soly. curve Vol- 48 No. 9 of Ca rnol%. bdate is characterized by an inflection pnint ' May 10, 1954 Lnja x. at it tem P. of 80 Bernard Rubin emistry. General and Phy6ical Ch '4 T, tied t 0 Alkali elemen and wmnovium.'~ A. Meerov V. Lomonmr, (1952) MNH#SOt, pcepd. by cristn. of ammool". sotns.~ of, pyrosulfate3, decomp. on heating and, ari t"OU1.11- b c formed into the.pyrosuffates. The temps.'vfthWtrans-_.. hemical Abst. formation to pyrosulfates-increa5es with increasing,ionik Vol - 48 Not 9 radius of the alkali clemmits and am Close to tbe't~Tps'. Of. conversion of the conesponding wetal hydrogen sulfates to 90 10 19 54 pyrosullates~ ..Bernard'Rubin Inorgani.c Chemistry 7' SPITSYE, Vikt. I.; MROV. M.A. 1 - - --, I\ Reduction of the normal sulfates of alkskli metals by hydrogen and ammonia. Zhur. Obahchey Khim. 22, 2079-83 952. Off-RA 6:2) (CA 47 no.13:6616 153) 1. N.Y. Lomonosov Sate Univ., Moscov. VIKTCR 1. SPITSYN Che~ical Abet. V0 L 48 No@ 9 *400 1954 Icidep Alkaliess'),6alte,.and Otbier H"vy Chemicialdi ir ca !-C. T nd dwod .----Poddm of MMO beftro- a. V. ;,,APiUYn..and 1. D. " (M. V, 17~4~&islc Ualv-., Ploscow). Dekkdy A&d. Nook V-S-S.R. W. 23W42(IMI ).-Cilanges of wt. an beating were An" Wilk 0.1-6. samples of the following coaqws, (Comte. In osides - D"rest Cv6rdinatioo fortnula): (1) 2-U LIOOA(h. I 1 .70 WO~- I" UP - Lislis (SI(WA)sl 14-fiHoO. (11) 2AM KOS002.15 WOOO-M I1rO - KJf,IS(WA)qj.W1*O, (MMISWSIOv. 12.27WO~-- 14.46 11#0 - 0411t (IV) 2.70 ". PA.23.76W%,17,76 UjO - KJf#IP(WA)sj.THoO; M ;.28 K#O.PA.24.17 MoO03AN HsO - Kella (P- JM*ANIAA H%O. In an air at Nowing at 4 1.11w., oatd. with 110 vapor at 200 (17.6 mm.). at 25*, 1 absorbed maWmmjindthelfO)&mtentrmlo2gmob. Domn;m. loon as 3.5% &W at M' the Ifto content was 16 mols. The HP content continued to fall with rishic temp. up to 100'. On further beating. the 1110 content falls Stepwi 'and at least 3 hydrates appear to exist. with 4, 1 A, and 175 110mols. The last 0.6 mols. are kept tenaciously on lWat- inx from 360 to 440'. The dehydration curves of a. IV. and V. an similar to me another: very little RIO Is lost up to IW*- t1sam appmr to exist a decahydrate and a penta- hydrate of 0 and a dodecabydrate and a hydrate covag. 6.5 If.0 of W. Above 100'. dehydration is markedly do" PWthK dthI741111tift of 13 1 IN 3 show. mA 0117modVin2stages. 11kWpsO-5HOonbftftt3W- 461)*; TV and V keep I HO at 24a-48DI &W la"WO rqW. M g" up Hoo up to."Mu'. when the am. of Heo 66 "a dows to 3 mols.; them is no further clehydradge up to , 3W0. Above 30% , q - 140 6 Just in a cwtimuous way; the mouohydrate is stable in the temp. 4"* &W the bendbydraU at 4W-W. in IV XT, W i. b6;.d more =Ir than in 1, U, and M. The bindisig of Uso 1 is Wifth )yrrpUccnwuto(KbyU,or*1KbyQ&. V- Is ClAydrated mom vally than IV. to 12 W. Uutmat with 1160 (at mom temp.) of the alto "Ydratod at 2WI. I wo found to givi a small amt. of hool. redibse; with n and; M this occurred only on heittiag at WO mW with JVU 2.18 MOXAM-91WOm.34-63 HvO - NasH6 IF- 6 WA)&J.1311.0, only above 3W uAcKatts an aumv beat-resistant thAn silleatu beat- ing to 5W*. the a ,Nxt. of the dehydrated tuagstate shows a 4 markeddelikitof 'OrcUdYttotheamt.o1a". Ulth. silicutunsstatts, sol. alkali silicate 6 found in tbt eat., and with V1, sal. phosphate. These findin coagpel a crit. attitude towards existing views an the constitution of birterg. poly campds. It is probable that. partly at least, 11,0 is bound within the coardinati. . N. Thou . . . . . . . . . . . . . . . . . . . R61LC Ong 0 th ti Igm mleilfti Vlkt~ I - 512' l Sk i G&S&Uf XWM., - "Akad, lVauk S. S,R. ~ 37-43 InT); cf.:C-4.48.318D*.- d( Mixts' of Nat and a t react below Me mp. of 0 % NalCOlatatm.*prcs=eoritt.vactioF. -MLxft.coutg.NA:Nb B. I and 5:1 kept for 2 hrs.. at M* (atm, Pve white melts which on analysis led i r Condit- to the &7 v ,1 he j sions: the 3, 1 mixt. had a little NajC0j left, more than 30%; In the former the loss of C03 was a little em than riquired for the formation of orthoniobate, In the tatter a little ftiore. It Is postulated that in the,3:1 mIxt. with the orthaniobate a little pyrontobate, NajNlh0j, was - ' mixt. a little Na2XbO&.' Similar preserit and in the 5:1 expts-werie caff fed out in vacuo. No reaction took place below 700%. at 900* the product of a 1: 1 inixt. itas a 7*6 saltandthatof the 4:1 mixt. heated at 800, DW. 1000,1100, :aiidl2OO.'w asthe7-6orthonlobate.- Theformerwascon7 . firmed under 700 magnification, the tatter by chem. Sealy. 51s;, y analysis ruled out the possibility of the formation h . metantabate. That metanlobate Was tot an In- NaNbO, iatie product was sbowu by heating 0c. ' * 7 h i r. Ftt a Na.M at 8 5 for I m.. pressure in t4cuo tion took plaa. 1. B 7~' %/The structure of some lsopoly, compoundi and hetuopoly Conipoumis, by the inethod of Ugged utonw. V. 1. Spke-yu. t..,Icetr. 7mli 8. at tht-Wffficture'at" If (1) as milioactive: Ind! h bchyavior, ~ at,,,., ht I Lq very muc IlepLudent &% the cl)46ctur of catioii in the oui~,idesphere, -bspe.cially on its* polarizatlint effect. , In 'the, casL of Ot PY ulfate there is it mol. cumpd. conventio designated NITS04SOx and In the cuse-of U, MOM Tilt'hy eclulvalpnt S atonis, lit NatAVA and Nh2W40;j, it was found by radioactive isotope Wm that all W atoms are equiv. In heteropoly compds,, HjSKWAN).IO,SHjO and HAP- (WAM41.16.5111a(U), at PH L$, only Ali of the'Watoms (Ire capable of topic exchange. However after a partial decompti. of ll~ at PH 4.4, the isotopic exchange is finished. In on- br. The Isotopic exchange of W between Naille (HAW30061MI1.0 und, HjjP(WA),j.I0.5HO is pmc-' L -11IL"Ad )YN.* VT". I ARes tl of ntQM=j_w&iIQA4qL with sodium hydroxide.. Wit, VWt. 1. vn and 11-W, Zhur. PMUd. Xkim. ~, gA-p . . -Nw-TTF-=rrYM)-NbA, Nallbo..3.5%0, and Nz,&Nbtr- OoMH,O wen fused with NaOR to proy an earlier pmtu-. late (C.A. 37, 229M that salts will result which upon treat-. Chemical Abst. nient with water will have a Na:Nb ratio of7:0. Asey- Vol- 48 No. 6 pected, fusions of 1: 1 and 7:6 salts with KaOR at SM. 450. * and 650 , lasting I I hr3., resulted in a 7: 6 salt (NbA 61 .2%. Mar. 25, 1954 IftO 22.12%, and NazO. by difference, 16.117%). ' Inorganic Chemistr of NaOH from fusion of Nb-OrNaOH could be removed only , y b_r digestion with abs. A01.1. The grayish powder formed- sl .)wed no cryst. structure under a 375 magnirication. Them ' l l h 2 al ~ I s of t e powder after drying to const. wt. at 1 0 ys ef Trsponded to the salt NaiNbOs. That 6; 1 -*Its mr. pos- $Lle was shown previously (C.4.25,=I; 34.4fP). Crys- Wfographic as well as thermal analyses prove It.- It M., VIO' d d l i ad 40S H i 4 N MP MO . . ro ves a a- ys s g at4 i , y ?Z1LOH. An npplIcAtIon'61 the Isotope e=bange 'method to-IW- stzucture study of aquapoly and beteropoly-comnounds. VIM. 1. Spitsyn end E. A. Torchenkova M. V. Lotionosov StZte-UnW.-noscow). Dakfady MaY Nook S.S.S.R. 95, 289-92(torn-rhe WIP& Isotope (designated W*) was used In the study of the relative stability of tungstate anionsinsoln. The purity of the isotopecompils. was tested by the. half-life detn. and the measurement of the wax. energy of the p-miliation. &.11co- and ptumphatungstic acids were prcpd. from the ordinary and W*. pam- and ructs- --tuagstates. The d8tible-excliatige reaction bct%vml the para- and metatungstates did not proceed instantaneously (contrary to Souchay,, C.A. 38, 62241; 40, 43101)., The ordinarY tungstate, anion diC not enter into doubt t-excatinge reactions with the heteropoly anions, wbile the hexatting- state anion of the par2tungstate did, which might indicate It to be the structural unit of beteropoly anions. Na pbos- photungstate and the acidified NatW*Ot soln. interact vtry rapidly while the crystals of NaW*O, met much more slowly, -than does the freshly formed paratungstate. Twolitteropoly coinpds., the radioactive silicophosphotungstie acia and the Phosphotung3tic acid, laterAct to an extent of only 20% in any length of time between 5 mia. and 240 firs. a' 11 U8 At high r pH. the reaction Is more -rapid. The bandin of the added ions in the inner spheres In metatungstate anions aLd the phosphotungstate anions appear to be quite differ. ent. W. M -stern ber z t N Irk 'A 1/7980 AppLyMG RADIOACTD---- METHODS OF WORK W Role pg !S. V. 1. 8 LA.=J -~u ~,PES MOT-g~ El ~64010v~~ Golutona. ULL- Ft 1955. 287P., P Russlzn) 30nva Conference) (Book on disp'&Y at &VA in in reseirch Wet, 'anunj Joi.workarn A6, top*%. A do- An 'radjoactivo tog Ith . ..... -to deal 1, ~topaj, methods hQvtus tndus I)roq~rtjaj of radlouOUVO idi ooription of the work wt adiatIOUG A" rul" th anpuring 6, p, y ri of n rtoticil ta~k3 in the 'lPPUjj;Aou of, radionative luotopor. rgdIonouve isotopes III borolstrY- A brlof I sulurBary precedes each task. (pbUb a UOIAJ Nt T~R SPITSrN, V. I. and SH03TAK, N. I "Preparation of anhydrous beryllium chloride on a larger scale laboratory installation by chlorination of a mixture of beryllium oxide with carbon", Khimiya Redkikh Elementov, No. 2, p 85$, 1955. A description of the laboratory installation in which a high purity beryllium chloride with a 90% Utilination of chlorine can be obtained,, as well as rawmaterials used and the method of operation. SO: D-413171 "A study of the process of chlorination of a mixture of beryllium oxide with carbon," Khimiya Redkikh Elementov, No. 2, P 93, 1955" The optimum condition for the chlorination reaction were: established temp. 900-95OPC, BeO to carbon ratio 2 : 1; briquetting of the mixtrue with subsequent ignition to 8500C increases the reaction velocity. the Maximum utilisation of beryllium oxide 89-9-2% and that of chlorine 84-89%. The linear velocity of chlorine has a strong influence on the crystal size of beryllium chloride produced. SO: D-413171 etho6 o ker! at Or-~ C0,M17)0~;,,cls b,; thM tire of 50' e 1055. 2 zurooean i .,.C-essio"~s) (_-,EAL), L-C. Vol- no. 1955, ii- List of Za5' 11ont! Z~ I ncl. USSR/ Chemistry - 1.1endeleyev's law Card 1/1 Pub. 86 - 1/35 Authors Spitsyn, V. Lp Hem. Corresp. Acad, So* USSR Title D. I. MendeleyevIs periodic law Periodical pr1roda 44/2, 3 14 Feb 1955 Abstract An account is given of Mendeivev's,discovery of the periodielaw and his. other activities such as the stucbr.ofthe periodicity of the spectra.of elements. The working of the periodic table is explained W'Ith ex~pieqi its usefulness in discovering previously unknown elerwnts is pointed -,oiit_, and the way in which-the existence of isotopes was-harmonized 4th..the 3aw.: is recounted. The structure of.the atom is also dealt with. Graphs illustration. Institution Submitted S, 4=211tlon of the structure and properties-VrOar, h te 11 a ern molybdenum and tunnten cotnDounds with radios cu,. Indicators. V Ritwl ~d YU 1. Its no -Ul Sank 104.25WO-~WI955); -449,15591i.- MOW Wlu. an d P#2v-re used in the study of the %V and Ho compds., Na,1141NN102006).181fto. Ni*lJ,jP(WA)a).- 16HA Hs(Si(hfoi00*l,7H%0,.aud Ua4P%VO.)MHO. ~7~- 71je rate of exchange vf'MoO, between the active NatMOO, and the inactive Na.H4(P(Af%Oy).j.18 ff,0i'at a pH 1-2- 11.0 (obtained- by acidifying with H14%) was measured in' time intervals of 15 min. to24 lirs. Itisalmostinstantane- ou3 at low OR valuw, and slower at lower addity. The rate of exchange of inner-sphere constituents wits studied with the lutca N.Lj(PWjQjMjJjO and the hiulive silicu- :molybdic acid in an acid solo., unit of the active luteo, phos hott ingstic acid with. inactive Nu3WO&. W. Mw-*- 5 e,~) % tt ~ 6 L~ '(X Q , ~ . 1,///~ 7 - .1 C ~~Yhe' investigntion of 'dAhALwjj= procems 0t SOM0 k I V t i 1. M And I IV, 1. it S"Y!341 77"MIUM).-The 11thYdr7di(IM of R hydinted K00~' arid W., Nfir. Cn, $7, Bit, 111111 11h hi-mijohatts wits Studied by hemins t1w !411t5 at'd plotting the Ion "f ond by delly,hadoin over coned. lliso'. The existing idens regarding the structures of the ni,)Wtcs (CA. 31, 3329) do i,ot secto to be correct. :Five to six 11,0 mols. are probably connecteq.1-vvith the aquapolyniab2te nudel, and participate actively in their structure. The last 1-2 tools. Of 1120 Must be e2pecially important in the fonnation of the niobate-mW complexes., W., M. Stemw-&- . - ------------------------ - -- -------- 77- USSR/Inorga.lic Cheirdstry - Complex Compowids C, Ab~. Jour R-eferat Zhur - Khimiya, No 2, 1957, 4io8 Author Kolli, I.D. Title Investigation of the Process of Dehydration and Thermal Decomposition of Potassium Silicotungstate Orig Pub Zh. neorgan. khinii, 1956, 1, No 3, 445-459 Abstract To study the isobaric and isother=al dehydration of the hydrates of 4-substituted silicotungstate of potassium f quartz spiral balance. The existen- (1) use was mde o ce of hydrates containing 10, 5j 1.5, 1.25 and 0.5 H 20 was ascertained. Most strongly are retained 0-5-1 mole H20- With such a degree of dehydration the salt adds reversibly 8 raoles of H 0. Final dehydration and 2 complete decomposition of the salt occur at 500P. Results of teasinetric investigation are in agreement with the data on dehycU-ation on the quartz balance. Thermal analysis of I reveals 4 endotherml effects Card 1/2 22 Card 212 2-, USS-9/1-norgaanic Chomi3t-rj Complex Compounds C_ Abs Jour Referat 'Diur f2) 4109 Author FolLi, !~L, Firogava, G.H.., S il '-n Vikt T Tit ie Dehydration of Sodium MQtatur .1-i- Pub ZI, . nporgan.. kh2.rdi, 1, No 31, 470--1L77 Abstracs Dehydrattion of sodiizi nattatiings-rat,2 (I I v a s, investigated by ooverall proccd-,Lres: on a quartz baianc~-; by Van njem.elun's method Ln desiccaiors over sulfuric acid of different concentration; on continuous operation balea- ce by heating in thQ air at different temporatures. Ascert,ained was the e%dstence of hydrates containing per I mnle of Na-,,O~ -,-o, 4-5, 2. qW, 2, 1.5 and 0.2-0.3 H 0. 2 Deter.Tu=d were the tc~rperature corditions of the existen- ce of hyd3:ates ai-A vater vapof tcnsions during their dis- soclation All the hydrat-es arc: soluble in wal;er:. after a con-oleto deh-1,dra,tion is no longer soluble in -w-ater. C,,ird 1A 24 USSR/Inorganic Cheiristry - Complex.CcmDoUnds C. Abs jouz- Beferat Zhur - Khimliy'a, DIO 21 1957, 4-,Og Over concentrated H2 so 41 1 forms a 2-hydrate, 9.8 moles of H 20 being remcv,~-d reversil-1), and 0.2 mole irreversi- bly. Most stron6ly are retained 0 2-0.3 mole HpQ; cal- culated on the basis.of the coordination formula L- quantity amounts to o,6z.o.9 mole. Na6H4 ' H2(W20-7 6-1 tilis Complete dehydration takes place at 2800. Card 2/2 25 .............. ------- - ------------------------ USSR/Inorganic Chemistry. Complex Compounds, C Abs Jour R-,fera't,. Zhurnal Khimiya. No b, 1951, 18841-, Author A.V Lepitskiy, V.I. Jpitsyn V.A. Pchelkin, Inst Title Study of Isotopic Interchange Among Salts of Nio- bic Acid of Various Iftes. Ong Pub Zh. Neor3an. Xhimii, 1956~ 1, No 4, 341-851 Abstract the iaotopic interchange in the he Iter.- Using NO , og"nous System of KlObli-37-27112) (7) ind IM )3' 2H20 at 200 was studied- The interchan3e between the precipitates I and II aud saturated solutions of I -and II occurs prLctically instantly in the a- mount of 60% and does not increase further in the course of time. The solubility of I in the saturat- ed solution of II is 0.0423 g/ml at 200. TL~kkng in- to consideration the constancy of the refraction in- d1ces of the initial niobates iind of tho bottom phases, the authors conclude that I and II do not interact one Card 1/3 -23- USSR/Inorganic Chemistry - complex Compounds. C. Abs Jour Ref Zhur - Khimiya, No 9, 1957, 30328 Author gpitsyn Vikt. I., Lapitskiy, A.V- Inst Title Thermographic Study of the Process of Interaction of Niobium Pentoxide with Caustic Soda. Orig Pub Zh. neorgan. khimii, 1956, 1, No 8, 1771-1775 Abst By a thermographic study of mixtures of Nb.,,05-(I) and NaOH (II), taken in different proportions by weight, it was ascertained that I reacts with II at.130 to form KayNbOs-(III), which Ts present in the PlIkall melt in equilibrium with the excess of II. It is shown that the niobates: NaNbOj-3-5H.-,.O, Na,#WAO.77-32H,~-O (17) and NaNbO3 interact at above 1000 with II to form III& Thus III is formed in melts containing excess II. The authors assume that the process of interaction of Na-niobates with II takes place with a slight exothermic effect but the latter is masked by the endothermic effect of the Card 1/2 USSR/Inorganic Chemistry Complex Compounds. C. Abs Jour : Ref Zhur - Khimiya, No 9, 1957, 30329 Author : Lapitskiy, AN., Spitsyn Vikt.I., Pchelkin, V.A., Simanov, Yu.P. Inst Title : Thermographic and Roentgenographic Study of the Process of Dehydration of the Niobates of Sodium and Potassium. Orig Pub : Zh. neorgan. khimii, 1956, 1, No 8, 1776-1783 Abst : Study of the process of dehydration of hexa- and metanio- bates: Na,,4R,X037.32H.,~P (I), Kj4Nb1,-;-OJ7'27HAO W), NaWbOj -3.5H,,,O (III) and KNbO,.2H,,O (IV), by means of a continuous operation balance, a McBain balance and a Kurnakov pyrometer. The existence of the following hy- drates was confirmed: of I with 6, 4 and 2 molecules of H ,,0, in the respective ~F~erature ranges, 80-1150, Card 1/2 USSR/Inorganic Chemistry - Complex Compounds. C. Abs Jour Ref Zhur - Khimiya, No 9, 1957, 30329 200-225'and 300-320'; of ii -with 9 (7), 6, 4 and 2 molecules of E(AO, the region of stability of the noni- hydrate being very li-mited, while the nther hydrates were detected at 120, 18o and 300-3500, respectively; of III with 1 molecule of H.%,O at 80', and with 0-5 H,;LO in the range 100-120"; of IV with 0.36 and with 0.2 11~,,O, at loo and 16oo, respectively. Roentgenograms of I, II, III and IV show a large number of lines. The int~irmediate hydrates formed during dehydration differ, in their crystalline form, from. the initial salts and are characterized by fine dispersion. After complete dehydration of I., II, M and IVthe roentgenograms show the sharp lines of anhydrous NaNbOj and KNbOj. Card 2/2 FGHELKIN, V.A.; UPITSKIY, A.V.; SPITSYN. Vikt,I.- SIMANOV, Yu.P. r---"- - - - . Thermography and radiography of the dehydration of hexaniobates of certain bivalent metals. Zhur.neorg.khim. 1 no.8:1784-1793 Ag 156. (MLRk 9:11) 1. Moskovskiy gosudarstvennyy universitet imeni M.V.Lomonosova, Kafedra neorganicheakoy khimii. (Dehydration) (Niobates) ISPITSYN, Vikt.I.; TORCEMMOVA, Ye.A. - Study of-the conversions of p-tungstate ion in solutions with the aid of a mixed sodium-cesium salt. Zhur.neorg.khim. I no.8:1794-1797 Ag 56. (MLHA 9:11) 1. Mookovskiy goeudarstvennyy universitet imeni N.V.Lomonosova, Laboratoriya neorganichiskoy khimii. (Tungstates) SAVICH. I.A.; PIrAYNY, A.K.; LEBEMY, I.A.; SPIT SYN.-Aktor Goxp;e4 compounde.of hexavalent uranium with certain organic substances. Part 1: Internal complex compounds of uranium with certain Schiff bases. 4ur,,Aqqrg._kh1m. I no.12-.2736-2741 D 156. (MM 1016) universitat imeni M*T'* Lomonosova, 'Isfed- ra neorganicheskoy khInii, (Gomplex compound@) (Uranyl compounds) (Schiff bases) FIXAMt A.K.; RYKOV, A.G-; SPITSYN, ViXtor ;,6, SAVICH, I.A. I --%an V.4 kit Complex compounds of hexavalent uranium with certain organic substances..Part 2: Internal complex salts of the uranyl ion with certain derivatives of 2-naphthol and 1,2-naphthoquinone. 4ur--negrg -khtm.-I-APoU;'974?79745 ID, 1.56.-. , (NLU 10W N:skOT~k:y 1. gosudarmtvannyy univernitat imeni N.Y. Lomononova. Wedra neorgAnicheekoy khimii. (Complex compounds) (Uranyl salts) (Naphthol) SPITSyN V I SAVICH, I. A., RYKOV, A. G., and PIKAYEV, A. K. "Ccoplex Compounds of Hexavalent, Uraniwa With Some Organic Substances; Part 3 -- Precipitp:tion of Ur&nDjm Frojr Aqueous Solutions by Mesns of Some SWostances Related to I.-Nitroso-2- Naphthol, " by I - A S avich, A - K - Pikayev, A - G - Rykov, and V. I. Spitsyn, Moscow St&'.e University, Zhurnal Neorganiches- koy Khimii, Vol 1, No 12, Dee 56, pp 274T-O~ It has been ezt-ablished that 3-bromo-1,2--~~naphthoqu:Lr-.onemonoxime-1 can be used as a precipitant for uranium. The precipitation of uranium with this reagent is ecoplete and takes place at pH x 2.7. It has furthermore been established that 3,,'~-dichloro-112-naphthoquJLnonamonoxime-1 cannot be used as areagent for the precipitation of uranium. Sum 1258 KAFUSTINSKIY, A.F.; KOZLOV, V.V., doktor khimicheskikh nauk. SPITSYN j - A R Hungarian chemical congress. Izv.AN SSSR.Otd.khim.nauk no.5:635-640 MY '56. 0(w 9: 9) l.Chlen-korrespondent AN SSSR (for Spitsyn, Kapustinskiy). (Hungary--Chemistry--Congresses) SAVICH, I.A.; PIKAYBY, A.K.; LIUMV, I.A.; SPITSYN,_,VAL-t,I. Synthesis of the series of Schiff bases formed from aromatic o-oxyaldehydes and heterocyclic &mines. Vest.Xosk.un. Ser.mat., mekh-,astron-,fi2-,khIm-l1 no.1'225-231 156. (KIRA 10:12) 1. Kafedra neorganicheskoy khImH Moskovskogo universiteta. (Aldehydes) (Bases (chemistry)) (Amines) 5 Ar 5,/r SAVICH, I.A.; ZELENTSOV, V.V.; SPITSYN, Vikt.I. Synthesis of the series of Schiff bases formed from 2-oxy-l- -naphtaldehyde and certain amlnes. Vest.Mosk.-an. Ser.mat., mekh.,astron.,fiz.,khim.11 no.1:233-237 '56. (MIRA 10:12) 1. Kafedra neorganicheskoy khtmii Moskovskogo univeroiteta. (Naphtaldehyde) (Bases (Chemistry)) (Amines) :> TOPCHIYEVA, K.V.; PESHKOVJL, V-M.; SHAXHOVA, Z.F.; AlIMARIN, I.P.; NOVOSELOVA, ,,;,.WTSENKO, I.F.; GERASIMOV, Ya.I.; NESMEYANOV, A . V . US _V!, A.N.; TMENT'YET, A.P.; POTAPOV, Y.M.; GIBAW, I.M. B.S. Przhovallskii; obituary. Tbat. Nook. un. Ser. mat. mekh.. astron., fiz., khIm. 11 no.2:205-267 '56. (MIRA lOtl2Y (13rahevallskil, Bygenii Stepanovich, 1879-1956) /Al ,,'USSH/Ttior~,anic Cheinlstr~j. Compl.ex Compounds, C Abs Jour : Refer~tt. Zhuriv-1 111udy4i No 1957. MN Author : Vikt. I Spitsyn, U.N. Shavrova. Inst Title Study o.C Hidrotis Co-litun Tantalates Orig Pub Zh.Obshch.K1iimiJ 195'6e 2"'. No 5,, 1258 - 1.262 A"Lbstract Sodium tante.LtLes wcre obtained by ~,:cmbliiizig Ta205(,) wi th NaOR (11) ia the we.-;~. .),,ht ra ti o I : II :: I : 5. The fused mcss ha-~-- LnU, beea washo-1 w'L th water in order to remove the sui)erfluous II was 6.j.zsolved in water heated to 800; the obta_~ned solid-' :;-.i was e-vaporuted at 50 0 tintil the cr_,-stall.~zatio?i started. Under these cond -i'tions, 8a,-_i2O.6Te20c-33H20 (III) was separated in the -form of heya,~ronLd -olates with uneTaal sides. When 0.1 of the ncrual solution of II was udded to the initial mass at a low tomperaturo.,, -a prec-_-pitate of IIL20*5'1'ap~) 22H__U (IV) was separated; this precipi-- t~_'te consiszs* o?_very little needle crystals of a Card l/P RINK-_ %USSR/Inorganic Chemistry. Complex Compounds. C Abs Jour Referat. Zhurnal Khim~lya' No 6~ 1957; 16824 prismatic shape. IV was obtained also by evapora- ting the aqueous solution of the initial fused mass at a temperature above 850, but in prisms of a larg- er size. d2o(3.58 and 3.78), refraction indices, PH of 1% solutions (8-58 and 8.48) were determined for III and IV. The interplanar spacing of III and IV is quoted. The authors arrive to the conclusion that it is possible to obtain two different compounds - III and IV - from the aqueous solution of I combin- ed with II, depending on the concentration of the superfluous II quid temperature. Card 2/2 -9- 7-. -7- ussR/Inorganic'6hemistry. CorWies Compounds. C