SCIENTIFIC ABSTRACT DAVANKOV, A. - DAVANKOV. A.B.

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CIA-RDP86-00513R000509810001-7
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December 31, 1967
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SCIENTIFIC ABSTRACT
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'Re emo I t .~ ? Da Vail i vi ) jkaO~a~ OWL 4 1. DAVANIN, A. I. 2. uss,,~ (600) "Calculation of Characteristic ifigh Water Levels." Zapiski po gidro- grafii, No. 1, 1948 (43-48). 9. Meteorologiya i Gidrologiya, No. 3, 1949. 4W Report U-2551, 30 Oct 52 DAVANKDV,, A. Magic grains. Nauka i tekh z mladezl, 13 no.12t~L8-20 D 161. t4 41 11 Ij 14 1, 14 It to A JO a b J? a U m b A *.A. I vVO(ow . , 11.11.Is ~.Vf I. ti ..I C V11t, 3. his study o( the fell i t s f4- t y a, usidation of bythurwImns (glaphths), 13. joubd t 11,11 hy hot the orpli ~ at the 110 i ff I . e "C ( A t an 1w mted with the u.,,g &mt'el tamable, it the Iattcf is "td with it ; (I X B JJ -0 0 . .. . KIM CI y It at 7. U. i'm the Sumtd. 110add, tkvmnr mul in I~nainr . ' , =00 4700 0 0 so* 00 tie 0 ire 0 .11 011 lei& ;00 it) A I 1 4 Ow 0 it --W a -76--o 3 1 U it A# 4"frItRION wit it I l1 a 11 0 10 0 0 o 4 ; 0 00 0 a 00 0 6 0 0 06900 0 In 0 : 00 0 0 all I j 0 S 4 1 0 a it 0 U w a 14 v 121) 14 v A& M-IX 9V U ;6 4 k 04D 90 1 00 . 00 c :-o0 7, of WIM *l6b. A. It, I)Avanku%* anil 1. S. - .00 RUN, 34IM"i Feb. 29s Miproducts tit exidatiou is[ pareMn wax nr of paraffin hy(fracailitt"S Are lf"IfThliftf,d .09 tit a "'ww 1,01M. 0 -00 0 00 0 :0 coo 00 -00 t:oo oo w is. 4 got 4 go t1 a Al 4 11 nun to x 1 0 1 : 1non Its 6 0 0 00 0 0 0 a 14 0 0 0 0 0 0 0 so 4 0 o al alto * 0 0 a 0 0 0 0 0 0 0 * Al 0 04 ;;;;;;*We oo* 0 0 9 ~TJ, - _a. 41 so lowl, 1. 42 40 M-. lm~v ltlil-w It 12 ]1 34 a It ;7 N s a gi~ A- 'a 11, 'A, "I 'A-AA N j6k A $1 Aj~ 00, 0 .1 f -00 -0 00 so V: 40 MAY 31, IOU. AcMs'&f&bwd-ln-tbc 4 =a( ,pd. Wt. vol. ad iml. their milt. In gasoline Ora andlarswirm-1, lio 0 & I ="O2fSOv,KO,.CI,orIlCl. ThehydruItyarids 43 S Joe see LAD 0 u log if 10 LK It Od 001 0 1 ff 14 2a 0 3 9 6 0 0 0 0 0 0 0 0 0 0 0 0 0 0 Olo 0 0 0 0 0 0 0 0 0 0 0 * : 00 900 1 00 oes 0 0 0 o go 0 0 & 0 0 0 I loss I A I ullutitilluty it m V n2fisi)l U. - - z . 1111- Do I A-- -z- - - - -4- .--- - - roccft Al 011011twilts IN thwc falmy sew by asidatim at parti& 9T, Trani. 17 Mra"fir Clingf. I'Aword. A m",r,193: 2. Pt. 1. W-77t)(IR35).-The re- A t f Fbhvr n cisidation under presiture -,jc verified SE 'dq;121,',!a,d,-d OF t., 0 "notti oiddatica Irtlip. was 1611". A %mall mr- 00 A-vitta". (if tile I-weeni, maii obtained "'). like list of Mn. Ct, Ctj and NI " cotillyst-4 A lilitfirf p(m. Influrner if tilffercrit catalyms wall oltwtvrd at lowet enaps. and Willi Im purr paraffits. AlIct upon. of tile midited paraffin 0 am It was Slutijecle-Al 14, but exim Willi lwnzrnc. "t. I jl~ were pfrid. 81111 111vt4ligatell. Two oll 00 .,%Id&tWn of diffrfirrit lioramil Inir"ll"Hatex writ 61iiri mitirliskm; slillilar, ))tit dalker lit-Itivi% tit a lowrt vatir were obtallird. 34D kv site a Qlj moxv i-1 -Ik- 0 -1 - .00 doe f7 to 0 too roe 400 300 0 bo 0 JJ.-JLA 017ALAUPG�CAL LITINAIVIll CLA%Sll'lCJk11C)w IVA 0 zc~- 106~ .41 S,,', UM -it.1% ow 'r;, An - I, bd Q It I I N to 0 AD Q 7) S U 11 AV to 19 U, It It 0 Ot a It 9 it IX K&O It i clit 0 0 0 0 goisi a 0 0 0 0 *1* a 0 411 4 0 a 0 0 0 00 000 :1 OMKISBAS m0 M0161126 WWI , 1 ' Ist tion of so-and AB Davankov IF Losev wa a tor r ra Artificial xe &i-4 AP Qr1goriev J ev- -- -1 J Fe ;h I Iya Rces, m5, Jotovs SY 36hinvhkin 0 l 00 . :12 1268-1 M, "he %m% of GervAn brigin eontaintod rbO 2.67, ee 40-4-1. N , N&20 -4'49 U4 org oonstitunnts 92.6% solid ratty Aa203 0.17p OW - acids suggesting:that the org constituents originate from the ago hydrolysis of b*eavax. !Goo off see SOO, see NOW III* VIV14019. moo. 60.14t Vow MOO'* -0 1 - M, Ili mil v its IF - w 2 Joe S is It 'N #a asm, 4k -00 Wo. set go POP -W'10",-.Wew, wzwl--v4- At I a It IT 13 it v 10 20 it v n if 13' .11 19 x it 9 iii. iiall L.11.--r- u v 9 1 V I A Psoctiscl ..c fee,[-Ft.l$ -'r. 00 -Luv. A. PbOllaCE41111 fecords. :09 00 c hAolclva. Rum 4fi.(,12. .% mhl, Ph and Na ults a (AtIv 11cm, A j~ j,t,jtnI %,Ih 1.1~ -id. 1-.dumd 1-Y --idat-im Of lwlt,,Ium .60 -00 Ti: -00 tri pat"11111 awl 1144%. 14 00 Poo 1:0 0 00 a 00 '00 ji J he 0 l iL 00 !31 ,AD 0 to i a METALLURGICAL LfTERATM CLASSIFICATION t I- too V " U It AV so Til,.- to to K all Its t e p 0 OT 0 0 0 0 0 9 0 0 0 0 0 0 0 0 0 *is ;-i- 0 ~ i ~ij 1 6 a I it '. o ~04 G q 1Y A. X_V&"wkvw 0. Ys. reactoys. - / 0l. 0. It Or#. chme 1. 'U", a v. ma g RISAK. m. 321. wm 086 t , 120. 140, Ow wit', son C at 1601 00 A IGO* #4w dwkmt %I Ijaw, with mid witbout cata- 2 Iy&U. BMW OWAL WM sod 25 kg -00 0 cu. M./hr: at a Fate cd 3000 1 " # 4 O' rm. Pic cstdydl,, pnpd. !j;ht intimvAian r! OIJ&AM at d .00 l of Pat 01F widu with the Imy ad 34m. 2,5% W Ca 160"Ime liathramits.t.fl.5%al .00 - o and 2A Al. of Parallin in lkit- * g the initial pe.JW tit udclatim. but thr A =S* CA~l4AU1OQCMCUVTC&tWY%t 6 f ~ no - 1 r CO. Tlk' CatAlYtiC SCOM U. 'b a coo go. feco" cWy at Imw tmF*. (WO md 1401) and nal at too all at Isr. me at ISO, mcdclat" Me O"tim a dm S JMV" lk-.-Vb, %Mgt 1430 only 15%01 14 Immue. CW. mag XG OGG 00 41 '111TALLUNWAL LITERA71101 CLASWK&TON golf., O-V of( Ma o N Is g t alitil Oc 0. 4 1 1 1 1 gi S G'g: '0 0 o "0 GO G 6 it o 0 L a, V TA a Of a I Of a 9 OW In, 11 0 0 0 0 0 go*** OOLG *Ibo G~w 0: 0 * 9 O's, iv** 0 0 GO 0 * o 9 a G, 0 0 000 v v w 1111 0 1111, v w v w IF V_; -;~ --- a Weevotoos, oot Poe 0 0 Of 0 0 0 it u to m a k it a 6 4i Aj 11 do a r 11-1 TI fit tAblet t 161, t fit I k-fl,I of 14111 0414b Hilo hysbot? 4,00 ' k t# Y "11" SCW SOM COMP Zee t. hydroay a" by cunt Inued ov k1stim with atin. 111 1441-01* It* 18 bra. In fhP Pfewl" I'd Mn ull* of 4: fall v grid. thr ronqj,", 1. .-stalysed at 120'. (hilviim- 000 14 1,,*tq 4"44141r) o6j. 014. f'.0.,eJ is The wol'"I 1.11,111411,111 CLAISIFICATICO, .20- v iv .0 at -~Oo a 00 0 00 9 0 6 a a 00 00 so* 0 i 0 C-Z- 00 00 00 0 0 0 0 0 000 00 4 0 9 0 9 9 0 0 0 0 0 0 0 0 0 go 0 0 6*61*017~~-;~ Is 1,i is b " )p ?. .w S. 1; -v 1W. 11-t,f., It molds for cdallas phenolic pleallf masm I. -N I%'. 00 ill A, J!, 11mapkiltv. kim, Apill :0, 111:1-' or Midt1% Itoni mixt. I,( high-mehisix mllu A as I', ; 700 IV .I J~tl.ilvlllll achIq With," willu"ll 11,14111. 4.1 IIA111101 00 80 00 00 300 '09 $10 tj too V 71 AV K) ll~ to 44 a it it a It It ft It I I lit is a 0 of 0 0 0 so 0 0 0 0 0 9 0 0 0 0 Cie 0 0~0 0 & 0 00 of goo a 01 0 Cie 0 a C. 0 0 0 0 o 0 0 a 0 0 too a L-t r re * um. AJAW"mwvsmW 4D. a (ft. 0". to" A.' m ).-Tho crude vtu so .,# 4WOlVed OA. " VC& of I&tola " we added, t6nowils it, &W the residue wombed With 10-16 ViAk -I# ta NtOH-.CA,,, wbon tar-fm god WAS is ob&aimd Is - 40--"% y1old. The w" Is hissabod bY L-L"- m4 106--l 16' for 7 hr. with KAAO, in I -T46F. R,00.-4% HNP.. R. T. 00 Lit -A - .9. 4-5- .,Po too see mn&LLvw.K&L Lnemooft CLUNOWMIN. *IQw olvioll" %low 6041mv lavago list am tra '00 -T 6 fm a 1 gr 5 a, 3 1 v 46 0 0 Ge 0 66,846990069 Go use ; ; ; ; i-ei ; It I a I * -A JL_x_A_JL_1_.L_ o: A so 00 It 060 of IDS a 00 1--k-t _w _~_ v ~ to if v a m A A i .1tres1slikation "d bloschim of montso *its. If,-,%- Ore. Chen). Ad. 7f 9( W. 31, IRIQ . 11jr lifix.%litur ditiliumv, Ihv It- A vlIvv1tt% A1141 111millbant% U10 till- isjwlatimt., itivillvell III Ilic TWOMY Of Illk'~ IRKI-1111- lilt' 491111C It'll W-14 tlk- 114,111" (it Idmablyl. Ow 11111-ml w1A1%.WiI% tlill~ 1-1 titol lilt it Ill w'.11 Ill togaita, It QlI. dot AV to all; If D- It to -0 o ST440 0 0 of e 0 0 0 0 0 0 0 0 4 2-1 -041.11 m all" III Ir Im 0 v 9 a a 3 4 o goo 0 0 0 0 0 at 0 0 0 0 0 mi a c so's life see see coo .00 coo ago see see '001 V v OOA WOO it ee'; goo Soo -Id 0- m00 000 X camp,-- 19N.+ Goo S IP-A cc gatntc N(N O* . Como H ;,~I b goo . y he t ml z coo woo WOO woo 1 WWI T I I we is - ON Wr .51 --- O&M - WON 1111 all =0 1-9 - 2.1 w ~ ~ ~ ~ ~ 04 04 ~ It r's 10 In , 0 16 0 0 *~* 6~ :110 '000ese 0 0 9 'a 0 go 0 0~ *f es 0 mbmb~a dbe&0-0 so a0000 - 6 wo o owe a aaWo o s - a AaA 0 0 0 9 00 0 0 go 0 0 0 0 0 0 o 9 0 0 0 *1* 0 0 0 0 G 0 * #1* 0 0 0 0 0 0 0 4 & a 0 . I I I I . . I ~ 11 t? It t., 1. 1. A ;1 1; .4 A 1. P A A It 11 V 11 is 3. 11 %1 PAL 11 ;-, L L L A j L 0 P AA t 4 0 t umialith from vegetable proteins. A. It.. -it % l .44 S. Ov te N. A. Askitoix,%it aml A. ' S. S. It.) 6. ?Ql-'.ki: 0 00 pmleins call Ile vtld. Itum witt-t-umitril Iwau ibmtr -mtg. 213% protci%60 by 4 altemair tremments Willi 11.2. h A XmIll %it,[ ppm. "it 0.2 N AcOlf ruttil. 1% CaCI, 90 1 lie 111.%lucl %lim %still 1AAIC1 add 441C. ;11.1 illit-li 11 all At 1%knal Irmp. hmm%" IMIC-I'I'mu th,wil't, om%. ' ,,"~ III() Milli #at*; w-Mily I'll . Its Illiki. 0%1111 0* j- '411,; t4 milk rawin wheti lircuscil in a hvdmilic lirrits antl 00 ilicit w4tvil Willi 3% CII,O formcd di.LS tVlllj~A(Ablt- it% zoo lbrorcIAIn mild 011crigib Willi file III ImIlivi a I)MAllard o0 11, list cum. talmlith.. 111,111C goo goo Go ~ 09 1 ro -U-&~ -., 4) at it is it ?I it It it .1 -tail it It "1 Aft L % a 040 13 1 ~ 4 go 0 ; 0 & 0 0 00 0 0 0 A 0000 0 * & : N 00.0 too** a 0 0 a 0 0 0 0 Si o * 0 0 1 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 Ts C9 . ~ f I sat""RL- A An ' POMINS Mop Wool#$$ OWN& ia d f r i 4 a a s n Nib Of 00 am d l g: p R T . . IT all&$% INS am* M 01 Sir IIOAQ Ift"tAl I a two dM4 -0g -00 log ve We 0 MWo 000 as* ale* NO* !10 00o W T-M *f A --m1 all I is I - -- - - -I ilociliFi-Aili- Peoria m A Mort 09 vm) from ow 0, A. 6 402-404). XCIWOTAWVAU~ Ifton-Nm mixtsm; a purer product wfth Wm savwt*, 10, w 6141 daft *0 110141111. yw& an, obtalmd by hr.). R. T. 00W AID.SLA ORIALLWICAL LRUA102 CLAWWWATON -UZ4-ft--A-j- 111000 MIP 04V Oat --J'alualt"ll 611111 OK G-V RT- - I I U AM A Al W 0 M V 'I IN 012as2livil U 0 0 19 11; ~ 0 1, 1, 0 a a " ; 4 - I" 00,00 6"wolo 0 wo nj: 0 0 10 0 0,04 WWO-e 0 0 *: * * -10 *1'* : a 0 9 9 0 0 0 0 0 0 0 0 11-4 Nei z6f pas goal ,1* 0 we* 1400 me 0 we 0 W-W--W - I I 1 6 4ft 9 IV A A) it 1) 1) M #1 16 if ONAC116M A*D P*C4'tdf't- -f~' -09 00 Acthratim of fte ozillatlan of Carriphefte. A. It. Da- ' -- ji A-stiltim.-and A. A, Berlin. J. Applird Ckrplt. (17~ S. R.) 12, JM-1011)(in French, 1406)(HOO.-Tbe 00 01111oldoll 4 Cautphrrur with Otte K.Cr,0,-llS.%(-I,-ll'o luillt~ ii not a ver Ifficlent olwatilm. The activation 4 ' i id I IN i l d N 114 1-00 00 lroul c ac QD an RN( the p"wess w th , lic" . N will investigated. 11N(% and NaN(h were the most of. .00 00 lective catalysts, The oxidatictin of catuphere was carried 00 Ir ~ *' nut with therillitt.of X.CrA8, 11,S0.22.6and wntff 69.5% ' . 1 . at all initial I I W d final temp. fit W 7M (14od should not be Thc spits. of 11 13 more Than 6 g. per of the oxidation mixt. anti l4.6%bywt.ofKjCtM,te%p. The oxidation was carried out in 4-46 cycles. Both of the above catalyms decreased the time of oxidation anti incirms-cl! the yield of camphor. NIL) th id i h i f N h f 11 on o ene e pre%ence o jul, t e ox at Esimp n & , Tbccxmph4v ; 06 ~t; ublaint i contained tMet, wriphomr. The oAjdatiun or Campherte under cowitions approximating (how which air ti%-qf in the indu%tty was aJw -Aff iud out ift the pm- - ld l f N NC Ti i f h 40 o or w&. 01VT ril'i a "~esuv o a e camp h. to y - M.1 anti M.6% ttV.. di%chning that an oxidatitia with i 00 t1w soniewhAt dild. mixt. took place although it frquited nd 34 hm r" but ti e llit Ti (22 5 ) f '00 . o more me . a l a ., p. , K:CrA used was smaliff than in tile oxidation with the '40 colurd. ruixt. The evolution of Cth during the reaction "% 4horv"I and in explained by the direct 00114tiOll Of tuphrur !0 C(N. A. A. PodVirny -00 tjo 9 A OCTALLUNGICA L LITERATURE CLAMPKATION S*IG*4 4AP 04V ONE 1111,111c"t! %I j VP 0 -16 P EN it a a a a X 9 of 0 n It 09 -5-7 r I ad a 0 1 W 14 1 a a KW 91 A AM I I a ' Kill- 3 V Will 0 0 0 16 a ; 0 0 0 0 : 0 0 0 0 0 0 0 0 6 0 0 0 9.0 0 0 0 0 * 0 0 0 0 0 0 0 0 6 0 0 0 0 0 9 9 0 0 0 SP *16 0 * * * 0 go 9 0 0 o 0 0 - _: : I ti-L A - 1~ L AA- 06 0 U P61k A. It. D-4vaiikov awl A, A. Plpflin. go Ru... Miamb *11,' 1011). A% a IAw (.w lJook- -00 1. wetf avetyltT1111141W All &1% 4mit, vis-ld. Vo Vo log too we I-is too %4.0- 0 3 0 v to to at K it 0 0 0 0 0 0 0 A a 0-0 0 Is pilla 21143S 141I)IM'11,11 all mu 1. 1, is "W f, tio-v. ~4-. r u u 'r I . . . . 4, . A, It, 1%vatikov go avid 0. A, Kotiovalovs. Run, 117,10M.fti. .10, 114t). Ilbril(l) 1. catalytically emulm."I wilb eldchy'le. ill 11W of nuintAn wax mfined by the narthod of C 1 -00 . . . 00 00- 00, zoo tiog a L A 6111titiMKIt tlltm-IL4f CLAWFICAMN ulve pe too All l, 4. 0 41 4 go, Aft 0. 0. Otte"O"O It 1 7 A M, r 4 R Ali PC 00 4 is W. Ovvtt.111! 00 00 -to .3 00 m if u so a U42- k 6 9 -A-L I k 4 L' I.t ..r, *0 lee Ta 0 TPO Belys"datid" vi"I derivatives um W MR. porstigalte. It. N. kuluv%kil unit A. U, KkImm I im 'F.m. AWN,, -he ka 1 19", NO. 2/3 W 0 Sim 44?Wfird With it% 11111c ab T the pitimilate Isit-ml an the wt. of I he fruminuier. he IkAytortimliun IKLKN-l'-d rapidly. NO offirr msluhifwr~ MIT urtAird anti the Consulfatr re-ithim wem easy tomtuu%-c frWU She pullyincr. 11W clo"llikonk under wbirit.puly- nkiisslion wa- carried out Wiln.. itrup. andAlamr) &'%,I Ibe characirrivi" of live protitwi (vWxrihy, =ItcWuq "fit, stay, in briuctic, cthy~mcliilc, amforsir. sk. &w -11fin.) or, WHAIAted. W Howh I ullit'liol CIL ano 1C .amor ILA is At to At V'_1 0 ~ it it it ;*mItNOWattitit 0 0 0 0 0 0 1P 16 At, 0 1 W a is a a 5 a V 14ifiv all 1% ' Is =ff! nix and I Kan (M I PC N . . y); rf, C.A, 34. % IU *t CM1141111c Ok'kU " Vnultidm wu I *W I s ., & 4 t ' . 2 0 ti kU b d h . mn Won raP m aft t Y t e rr"tk-n without 41 .,- u c uW&v Ace witb a yW kwgvw 44-7-, at this tv.p. )' M-7 I Th I !I5j ~n4 n e ,fiI , ( uji * . a! to oil 110 j(j e. C4 A., On. Of, t* f 4 too tie Isom 11VIVISY" loom VU411tv , - v80480 us, low Own d" 44119,1 am 4mv All -~* - - V AA I t a im 0 N w 1 0 IN 9 3 4 Am ; ~ ; V J t rim I 11 I. I 0 so* 0 a 0 * 00600.00 0 0 ft 0 0 & 0 0 l a seel 0 0 00 goes 0 1 .0006 **so*** 0% 'Pas Oq_; .4 Dayan 00 SW D. Va. Pmpb. X". iltv". tustaw 14; ;Q;m I, oil 41 ~ -1- 'b. b. i-- Doi Slow s0'% use: L A StIAL LV"KA% MfNkl$AlCLAMWVATOM 61"s 4" VOUSAV Wei SMADAID .11 4mv ass musin 824121 da ww Us u a Ts' a' 'a I W. s A 4 - 2. A-'U 4 0 f ,14w, e o* 4) 00.0 so's 6 goes 04 0 0 0. * 0 0 4 it Al " ' ' . s 0.0 0--o r t-0 0 a O o DAVAMOV A.B. kandidat takhnicheakikh nauk; PRUPIS,D.Ya., mladshiy . 0 , nauchn" Botrudnik Lye-resistant abrasive materials. Xhim.prom.no.2-53-54 F,47. (Abrasiv )~) (KRA 8:12) A. 1) fty, A. . i ~OA vm'u'kur. ~P,41",-,Kkfm by cmullim Pot;"-Ii" W Stylent or copoly"Wristim al goptkyj mothmay to and vinyl actlate with (NIIJAA as a Catalyst. 7U p Womadeq-dw is the I, dyes (0YOW . W moolkyle"u) too the dia- vicift. log pracm rmh boo cbem inter- =-betorlubmactbdelbimic dyes= Mk piy~- Two- "aaclusion was bmd *a tM haverims obkmdo-: (1) The um of PUM&Ae mtslyst produces ,-haracter (1-4 am Sim or pDaymmor is pptd. an clamtka OFTIOR camW COOMPICK b" a high the Z;;. .1 U4M MA Chem. mactlim. (4) polpmer dimmalm in are. "twoutste som cVWW win& c"m in the am at SMI its in ukkk the beak dye by iWI is prmtkaUY IDW- H. K. LAvinpton DOININ, M.N., skademik. otvetetvennyy redaktor; GAPO, Ye.N.; GAM, T.B.; ZOEUMINA, Ye.S.; WHINSKIY, V.V.; BIWIKAYA, I,M.; SLIUVAIVA. G.M.; ROGINSKIY, S.Z.; UNOVSKIT, N.I.; F=. N.A.; K=W, A.V.; NZYYABI, I.Te,; SLINYAKOVA, I.B.; MUTSIT. F.I.; U)SIO. I.P.; T.ROSrIANSKAYA, Ye.B.; TIOLINA, A.S.; DAVANKOVI, A.B.; SAWAM, K.M.; BRUMBFM, Ye.M.; IMKOVA, Z.V.; VZZWVA, Ww.VIT!95W'SKIY. S.A.; MIMYLOVA. Ye.ii,-. KAZANSKIY, B.A.; RYABCHIKOV. D.I.-, SHWAKIN. 7.M.; EMOVICH, V.L.;BUNDILI. A.A.; SAVINOV. B.G.; VZW. V.P.; 3PSHTSYS, Y&.A. [Research in the field of chromatography transactions of the All-Union Conference on Chromatography. November 21-24. 19501 Issleaovaniia v oblasti khromatografft; trudy Vseooixtznogo soveshcbaniia po khromatograf-"L, 21-24 noiabria 1950 9. Moskva. Izd-vo Akademii nauk SSSR. 1952. 225-p. NLRA 6:5) 1. Akademiyu nauk SSSR. Otdolenie khimichaskikh nauk. (Chromatographic analysis) DAVANK01r, A.B.; SOKOLOVA. Ye.A. C"ting properties of awalsion polymethyl methacrylate. Zhur. Prilclad... lhi.m.. 26, 217-20 153. '(Ww .6:3) - (CA 47 no.21:1179~8 15)). WA-1 R=nkov, A. AA1W_ "Ob Isbiratellapi.adsorbtaii krasitelei iskusstvernyni e adjRrbtion of- y s .yn affio ami") Selectiv thetic resins, Zhar. Prikl. Khirtiis. Vol 26, No 12 pp 1,299-90,l .Dec. 1-953 Study of dying bydkophobje,resins by,aqueous 86114tions of organic dyes. It was found that the polymers of,- Ivinyl chloride, in presence of peracidic substances exhibit pronouncpl sid 'soO~ttveproperties with respect,to basic dyes's Acid and dinct'dyes do 't" no extract tolyvirWl chloride from its aqueous solutions. It is possible to separate It4susing polyvinyl chloride. Chemi- cal similarity between basic dyes and polyvinyl chlokde indicate the presence of furctional groups. DAV 01T, A B. --Ne-W-M-OW073 of dep anol nofindust wastwwaterz.-~ "7- P2 A. B koy and eva 1. 'Met-deleev mmW . G(OtANA 9 -.Vftffff~ , 1939, Tn-ii-ex-EFE-nge r-eilns are'sathfactory fo r the re re oval 61 ghenols from'samples of Industrial waste liquor.b,.j the la . scale. The most satisfactory renins of IoWjnanuf;,Pxe MP\FKh, N-0, TN, PH-9, and EDR-10. Poiregenemflon of the mini, the soIns. of NaOH or N11,011 areused. The: conc-n. -4 phenols in the regencmdon liquor Is btlow 12%, G. hl, Kosolipnff DAVAINOV, A. D. "Concerning the Extraction of Nenol Fron. Aqueous So-3cutions by Yeans of Arl:,-ordte Res ins .H an article included in the book It-The Theory and Practice of the Application of Ion-Exchange Agents 11 edited by K. V. Chmukov and publi.shed by flip AS USSR 1955, 164 pp. P PAVANKOV, - ~-~ Selective adsorption of dyes by synthetic resins. Soob.o nauch.rab. chl.VXHO no-1:32-38 155. (MIRA 10-10) (Dyes) (Adsorption) (Resins, gynthatic) K A - CS, USSR/ Anrlytical Chemistry Analysis of Inorganic Substances G-2 Abs Jour Referat Zhur Khirdya) No 4)~1957o 12045 Author Davankov A.B., Laufer V.M. Title DeteriAnation of Precious Metals by Means of Ionites Orig-Pub Zavod. laboratoriya, 1956, 22) No 7) 188-789 Abstract Snall amounts. of Au.and Ag (fractions of mg per 1 'iter) are separated1rom cyanide solutions with an anionite. So 5. oixtaining KAg(CN) or HAWC14, is lution of PH 3, a passed throud), an cadoorption colmm fiiied with anion- exchange resin NO in thb chloride forn. In tho case of solutions containing 0.5-20 rg/liter Au., fed into an ad- sorption colwm 7-8 rzi in diameter, with a resin layer 250-300,i= In depth)_rato of filtration must not exceed 15 ml/n, inut.e. - With. solutions, containing large excess of mi- neral.salts Ororganic admixtures the rate of filtration Must be decreased. The amount of solution that is filtered through.the adsorbent is detemined by the initial Card '3L/2 t fir'n of -etq tic ei. I from - L 11,9 - ,77 , ; t V . S 1 . IMM . ' I V AM v. M-L-'aler. !howa rAt highly pnrtyas specumem uf -luade UU43a "t1tallp ;-eArs vvc-re e5e~~tjve in exin. of Au Ir,,in waste liquo-ri, AJW combustion of the ruin, from M%~ to 100% -flu was rccDvtytJ. The baQe liquors wete made sliglitly urid with IICI und -,-t: th, puwd. rt.4iis 1 5 lirs.,afte; which the r,~iL'uiu wa, !~cpd, wa-stied, mid ipiAvd. G. M. Ko-~Iaj~"ff -2" DAVANKOV. A.B.; LAUM. Y.M. Ion exchange and the distribtuion of gold ions in repinous absorbents. ?Svet.met.29 no.11:1-6 N 156.. (MLHA 10:1) (Ion exemage) (Gold) . . . .. . . .. . , ds"-Wo ate V XIAilf# (2h. PW. Rhim 1959 A imssins, in byar 4 (1): CW a) and sulphato (IM formr, vrith grain si2ee 0-5-*-8 mra.. Were used $or too recowry of gold irom. yum sq. selutions Lq Y-AujCNj and tom indus trW wast6 (chlay from plating bsth3). - 1 ,nth filt-ation rate gold In YzIntlom vras 24 mg,/L. p1l 7 -, Amovnt 0 ' !~S,Dw, recovery of gold 10 ml-jmiz and -E =i layer d th 190 mm - R th d ~ 9 ~ !W ep en resiz eld-d 1 vrAs achi-yed 1~y U; I and %. 3 8S797-22o-'-J' md 74-215,~ ns 77 cab " A. t, ka ' 7-7- 77- -77 7 . 'if ' :~ J~ ZT~-- 7 7 DAVANKOV, A. B. CHMUTOV. I-V-;otvststY*nAYY roda*or; SHRMYMN.;Y.M., profesRar, otyst- styanVy rodaktor,- WAX rodaktor; RACHINSKIY Y.Y., redaktor; SAIADA Ir.,X.M. rodattor; bmiov, P.L.,Iprofeseor, re- daktor; TROSffANSKATA. Ye.V., professor, redaktor; 73GOROV, N.G., redaktor izdatelletya; ASTAYIYIVA, G.A., tokhnicheskiy rodaktore* [Studies in ton-exchange chromatography; work of the conference an the application of Ion-exchange chromatogr&pby in medical and food industrY3 Isslodovanila v oblanti lonoobvencoi khromotografill trudy soveshchaniia po primen-aniiu tonoo*bmennoi khromatografil T meditsinkoi i pishchevol promyshlennoiti.' Moskva, 1957- 193 1P. WaA 10:6) 10 Akadeadys, nauk SSSR.Komissiva po khromXtografii-2*Chloz-k*r- respondent Akadeall zauk SSSR (for Chmutov) (Ion exchange) (Chromatographic analysis) SOV/137-58-8-16648 Translation from: Referativnyy zhurnal, Metallurgiya, 1958, Nr 8, p 58 (USSR) AUTHORS: Davankov, A.B., Laufer, V.M. TITLE: Recevery of Precious Metals by Ion Exchange and Secondary Processes Occurring in Ion Exchangers (Izvlecheniye dragots- ennykh metallov s pomoslich'yu ionnogo obmena i vtoriclinykh protsessov, osushchestvlyayemykh na ionitakh) PERIODICAL: V sb.: Materialy Soveshchaniya po primeneniyu ionnogo obmena v tsvetn. metallurgii. Moscow, 1957, pp 73-79 ABSTRACT: A device for saving Au from industrial caustic solutions by adsorption on anionite resins of low swelling capacity, porous structure, and fundamental properties favorable both to ion exchange and to adsorption, has been developed and tested suc- cessfully under industrial conditions. Dissociation of such anionites in aqueous solutions with formation of cations of low mobility facilitates coagulation o-f-Au and ensures speed and completeness in precipitation thereof on the adsorbent. The resin is separated from the soluti4by means of a Nutsche filter. Joint ion exchange and reduction by hydroquinone was Card 1/2 applied to Ag and Au solutions. This significantly increased SOV/137-58-8-16648 Recovery of Precious Metals by Ion Exchange (coijj~ *) 7A the absorptive capacity of "H-0" anionite and made it possible to extract up, to 112.856 Ag and 114.6% Au relative to the weight of dry resin (and this did not even exhaust its absorptive capacity). It proved possible to extract up to 721o of the Au in sea water when 50 g resin was used per 500 liter of solution, but the resin was contaminated by Fe salts. The "H-0" resin is suited to re- covery of Au frorn highly- contar-ninatcd, exhausted caustic electrolytes, but regeneration of the resin by the usual means is not possible. "H-011 resin permitted the extraction of 80-901o Au from a solution of Au resinate in turp- entine containing 3.5 g Au per liter. Ye. Z. 1. Gold--Recovery 2. Silver--Recovery 3. Ion exchange resins--Perforniance Card 2/2 g P -4 A ioti Ail from a d ar t '," ge an q. F At V. us itivt-sti. roup .. g 12% On SwOrmg ld 13!~ in vot b d 1 . . ' y Fri I' Mnd AgNo) Was Mle a( irk it P M rhe end of the =W -iey6e, baviiiR ui~, rba' b ~- ~ 1- - AgNJ-..Zh "T"z pv.7iods Irm 3 hr~ if, ys -I ll~' !v5il: Was -Asll~ ~ilh - lbu ChlVridClX-MkljO4lLSj-J.C it lo ]l 3 5 . ing 7p Mitred Ifirbugh the V~Jatmj, jkn aad G.~5~4 g~ ar -of ris:n -5 U.); Az were, AUTHORS: Davankov, A., B., Zambr07skaya, Ye. V.9 SOV/156-58-2-42/48 BorzeUova-,-T.--Y&. TITLE: On Granular Polycondensation and on Polymerization in the Production of Ionites (0 granullnoy polikondensataii i polimerizateii v proizvodetve ionitov) PERIODICAL: Nauchnyye doklady vysshey shkoly.Khimiya i khimioheskaya, tekhnologiya, 1958, Hr 2~ pp- 369-372 (USSR) ABSTRACT: The shape and the physical properties of the particles of the synthetic resinslused as ionites are of great importance for practical application. Most of the ion exchanging resins have with hitherto been produced as grains of irregular shape (' sharp edges). They are obtained by crushing the solidified polymer. The 10 - 15% of dustlike waste forming in this connection oannot (with one minor exceptiong Ref 1) be properly used in industry. The costs for their ap lication as fertilizers in agriculture are too high (Ref 23. The Polycondensation mentioned in the title is based on the Card 1/3 solidification of the polymers in liquid state. Thus, crushing On Granular Polycondensation and on Polymerization BOV/156-58-2-42/48 in the Production of lonites is not necessary and the waste decreases to 0,3 - 00~- According to temperaturey intensity of mixing and the properties of the surface-active substances in the solution, ionites can be obtained as spheres of different size. This shape of ionites has a number of advantages as compared to that of the irregular grains, The problem of the methods of production of such spherical ionites has not been sufficiently elucidated in publications (Ref'3). The authors made it their object to produce several already known and several new anionites of spherical shape. Final solidification was obtained by an additional heating of the polymer in liquid state in different media: oilep benzene, glycerinc, saturated NaCl- and CaCl - solutions and others. The test results were 2 Obtained by using transformer oil as solidifying medium. On contacting the oil the polymer drops are covered by an oil film which prevents the coagulation of individual drops and thus the formation of greater aggregations. At a temperature Card 2/3 of 6o - 65 0 and with intensive meelianical stirring On'Granular Polycondeneation and on Polymerization SOV/156-58-2-42/,18, in the Production of Ionites (propeller mixer 200 rev/min) solidification of the drops was completed after I - 1,5 hours;in conclusion further conditions for an optimum quality of the spherical ionites are given. There are I figure and 4 referenceaD 3 of which areSoviet. ASSOCIATION: Kafedra tekhnologii plastmass Moskovskogo khimiko- tekhnologicheskogo instituta im. D. I. Mendeleyeva, (Chair for Technology of Plastics of the Moscow Institute of Chemical Technology imeni D. I. Mendeleyev) SUBMITTED: October % 1957 Card 3/3 DAVARKOV.,.A.B.; LAUFM, V.M.; RAZGILIIMYZV, N.Ye. Extraction of gold from discharge electrolytic solutions by ion exchange. Zhur.prikl. khim. 31 no.3:494-497 Mr 158. (MIRA 11:4) (Gold) (Extraction kCii;6-mistry)) (Ion exchange) SOV/136-58-5-15/22 AUTHORS: -D&yaglec-ov, A. B.,_-Lauf er , V. M. , Tarusin, V. P. , neginsk-ij, O.Ye, and Ruzhnikov, M.S. TITLE: A Pilot-plant Scale Experiment on the Extraction of Gold from Ion-exchange Resins After Adsorption 1Foluprox.ysh16hnyy op~,t vydeleniya zolota iz !C'-_;cobirenny1&. ,sir-ol posle adsorbtsii) 91 PERIODICAL: Ts-t,-etnyye Metally, 1958,Avr 5, pp 81 - 82 (USSR) ABSTRACT: The authors discuss some examples of gold recovery froo- ion-exchange resins being effected after ashing the resin, They describe work at an enterprise controlled by the J_ -ry oS the USSR) Minizterstvo fina:nsov SSSR (Finance ",Jnist in wbhh gold was extracted frwr- spent el%~,ctrolytes '~.-Lth the aid of type N.-O resin in two 1 665-4= high tubes (73 mm dia.) in series. 9?.6 litres of spent cyanide electrolyte was passed at 10 litres/hour and an ash containing ?3% gold was finally obtained., The Cold was extracted from the ash by high-frequenoy melting under borax in a graphite crucibla in separate portions. The experimental data are tabulated, showing 99.8_10jo' recovery of Card 1/2 SOV/136-58--5-15/22 A Pilot-plant Scale Experiment on the Extraction of Gold from Io--- exchange Resins After Adsorption the gold present in the original solution. The authors found that with careful ashin in ceramic vessels and fusion under borax, complete extraction of the gold from the ashed residue was obtained. There are 1 table and 4 Soviet references 1. Ion exchange resins--Adsorptive properties 2. Gold--Processing Card 2/2 3. Gold--Production 4. High freWiency heating--Applications DAVANKOV9 A. B. [Grigorii Semenovich Petrov) Grigorii Semenovicb Petrov. Moskva, Izd-vo Moak. khimiko-tekhnologichaskogo in-ta, '1959. 3-1 P. (MIRA 16:11) (Petrov, Grigorii Semenovich, 1886-1957) nrv 5(2), 18(6) 0" '1156-5j`-1-52/54 AUTHOPS: Da-vafflzov, A. B., Laufer, V. M. ----------- TITLE. On Kew Methods of the 10"oncentratic,n of Gold on Ion Ex- chan,,~ers by the Ai& of Ion Excl.mn-c and of red,;x rrocesses (0 novykh Imetodakh kontsentrirovaniya zolcta na ion-ita-kh s romoshchyu. ionnoco obmcna i olcislitclino-voss'uaiiovitellnylch protr'0200v) PZRIODICAL: lohlady vysshey sh'z-)ly. Lhimiya i khimic~hesk-nya tehhmlil -:-iYa, 105", 17r 1, pp 21(;2 - 2o5 (US---'-L1) ABSTRACT: The ads~r-, tiGn of the gold saits -!AuC! 11 and 1.aAu (C'7) 2 on synt"otic resin anion excham,ers 1111-011 and "TN", and t'lle elution of those salts by thiourea or J-j,rdrC,chlc,:Lic acid in acetone and athyl alcohol are invcsti-7ated. The results are listed in tablcs. The com-olex AuCl- salts could be 4 reduced by hydrequinono. Thio reduction re-liborzat~os the ionoacnic groups of 1j-' e excl,an~;er and re-establishes its excLa.-.,-e cno~acity. *.-iith the Au(C1T)- -ions the reduction 2 c(.1uld no[; bo. effected. Th,,;r3 cn-ltj cuuld, h-~-wcver, be ro-:ii.--vod Card 1/2 from the resin by wonk basic soluti-ons or by Y,--ncral acids. - V llr6-~~ 9-1-52,154 ()-i Nev Illethods of the concentration or Gold on Ion j k' / ', and rs by the Aid of Ion T cf Redux P-occs~;~s D,cl,ai --c 0C.1"(1 not, bc offectud --C'1(1 Uluti~ "i In (JUP-11titative (Te.bic). The tutal gold ccntant Could be jrc.,,--,rvcd only by u the burnin.- uf tl,'c rcsin. There are 2 t,"bics -nd 71SoViel references. jr,frij plastmass A S S -C C I AT D- I iKafedra tchhno '-3.c;'eskcsjo instituba im. D. Tcc'~ J:jolo3y of -Ilasticsso-' tile tif Ch'Otical h TcchnoloLy ineni D. I. Mendelayc"r) !-'ay 27, 1'1~58 C ard 2112 5(3)915(8) kUTHORS: ,,,,.Davan.kov, A. B., Babehinitserp T. M.9 SOV/156-59,0-5-7/48 t zenk6*i"----- TITLE: Innergranular Chemical Transformatiom in the Copolymeres of Styrene-With Divinylbenzene (0 vnutrigranulInykh khimi- cheskikh prevrashcheniyakh v sopolimerakh stirola s divinil- benzolom) PIRIODICAL: Nauohnyye doklady vyashey shkoly. Khimiya i khimicheoXaya tekhnologiya, 1959, Nr 2p pp 363-367 (USSR) ABSTRACT: The authors investigated two forms of the chemical reaction in the polymeres mentioned in the title, which were used in granulated form (diameter 0.25-2.0 mm): 1) Nitriding wfth following reduction of the nitrogen group, and 2) Chloro- methylating with following substitution of the chlorine atoms through aminogroups. Copolymeres with a content of 2P 39 49 and 10 % divinylbenzene were nitrided. After nitriding, the nitrogen contelit avergged 12-14 % (Table 1). A high content of divinylbenzene aggravated the nitriding and resulted in a lower nitrogen content. The nitrided granulate was of yellow color and its mechanical hardness decreased. The reduction Card 1/3 was carried out - after am unsatisfactory trLal with zink - Innergranular Chemical Transformationsin the SOV/156-59-2-37/48 Copolymeres of Styrene With Divinylbenzene with tin (II) chloride in hydrochloric acid. With increasing interlacing of the copolymeres, the force of the reaction decreases (Table 2). The static anion-interohangeabil'ty of the best resin test-pieces amounted to 6 25 mg-equiv/g for 0-5-normal hydrochloric acid and 7.75 mg:equiv/g for 0-5-nonmi sulphuric acid. During the second series of tests, copoly- meres with a divinylbenzene content of 2, 4, 6, 8, and 10 % were treated with chloromethylether (Table 3) and their chlorine content was determined. The copolymeres with a Cl-content of 18-19 % were substituted with trimethylamine. The rest-content of chlorine amounted to 7-10 %, the nitrogen content to 2-2-5 %- When treated with pyridine instead of trimethylamine, the copolymeres contained 9 % chlorine and also 2-2.5 % N. The static anion-interchangeability was 2-3 mg-equiv/g for 0.1-normal hydrochloric acid. There are 3 tables and 4 references, 2 of which are Soviet. Card 2/3 Innergranular Chemical TransformatiorBin Copolymeres of Styrene With Divinylbenzene PRESENTED 13Y* Kafedra tekhnologii plastmass gicheskogo inbtituta im. D. 1. Technology of Plastics Moscow imeni D. I. Mendeleyev) SUBMITTED: December 11, 1958 the SOV/156-59-2-37/48 Moskovskogo khimiko-tekhnolo- Mendeleyeva (Chair for the Institute of Chem.,cal Technology Card 3/3 _S10- 81/'60/000/019/00'1/0 12 AOO6/AOO1 Translation from: Referativnyy zhurnal, Xhimiya, 1960, No. 19, P. 522, # 7936.9 AUTHORS-, - Davankov, A.B., Zambrovskaya, Ye. V. TITLE: The Use of Acid Esters of Dithiocarbonio Acid as a New Type of Ion-Exchanging MaterLal_~ PERIODICAL: Tr. Mosk. khim.-tekhnol. in-ta im. D. 1. Mendeleyeva, 1959, No. 29, PP. 72-b2 TEXT: The possibility was established of converting watier-soluble salt's of various acid esters of dithiocarbonic aoid (ethyl and butylxarithogenate of potassium, cellulose xanthogenates, 'polyglycerins, poly-viryl alcohol and its copolymers with malein anhydride) into a non-soluble form by means of adsorptlon on. the "H-D" resin. The authors studied the exchange capacity of ionites ot.- Ways were found of tained under dynamical conditions from AgN03 solu4_'(,_"s- 3oncentrating on the aforementioned adsorbents gz~at amoun-ts cf silver with the use of reducing agents (19 - 31 mg-equ/s). A zynthe,-is was di~veloped of a con- densation. MMC (MMS) resin containing sulfohydril groups (5.76% S) . Investigat-iMS Card 1/2 S31/0 81/60/000/019/007/012 A006/AOOI The-Use of Acid Ez-'-",ers of Dithiocarbonic Acid as a New Type of Ion-Exchanging Material were made of the sorption capacity of the resin (granulated and non-grarulaved) with respect to Ag cations at 20 and 60 0C. and of the possibility of-extracting silver vat of the column. Ye. Zambrovskava Translatorts note: This is the full translation of the original. Russian abstract. Card 2/2 S/081)ra 1/000/00 i/b 14/0 17 AOO~/A105 Translation from, Referativnyy zhurnal, Kftimiya, 1961, No. 1, P. 515, # IP39 AUTHORS- Davankov, A.B., Davankova, D.A. TITLEt On the Problem of Chemical Transformations of Polyvinyl Alcohol PERIODICAL: "Tr. Mosk. khim.-tekhnol.,in-ta Im. D,1. Mendeleyeva!', 1959, No. 29, pp. 93 - 98 TEXT: The authors investigated some chemical transformations of polyvin-yl alcohol. Hereat benzyl ethers of polyvinyl alcohol were obtained with a high con- tent of benzyl groups (66.4%), and their properties were studied. Chlororhethylat- ed derivatives of the benzyl ethers of polyvinyl alcohols were obtained. It is establishqd that the disintegration of the polymers in consequence of nitrating of the benzyl ethers of polyvinyl alcohol and subsequent reduction of the nitro gr,,-)ups into amino groups is observed, which leads to compounds that are soluble in alkali hydroxides; highmolecular quaternary ammonium bases with exchange capa- Cara 1/2 S/08 1/6 1/'000/002/0141-117 AQ05/A105 On the Problem of Chemical Transformatio~is of Polyvinyl Alcohol city for 1 n-solution of HCl 1.5 mg-equ./9 were obtained by chloromethylizing of \j ordinary benzyl ethers of polyvinyl alcohol with their subsequent treatment with trimethyl amine hydrochloride. E. T. "Iranslat-orls note: This is the full translation of the original Russlan abstract. Card *2/2 ZURAKOVA, L.B.; PA!~~OV~ A.B. Chemical conversions In granular 2-mtbyl-3-yinylpyridine-divinyl- benzene copolymers and other cross-linking agents. Trudy NMI no.29:99-107 059. (KIRA 13M) (ftlymers) (Pyridine) (Benzene) DAVANK07, A.B.; ZAMBROVSKkyA, YO.V. Extracting silver by ionitem modified by the adsorption of xanthic acid. Izv. vys. ucheb. zav.; tevet. met. 2 no-3:82-C8 '59. (MDLA 12:9) l.Moskovskiy 1-.himiko-takhnologicheakiy institut, Kafedra tekhnologii plastmass. (Silver) (Ion exchange) DATASKOV, A.B.; LILUM, T.H.; RAKITIN. S.V.; LVIAN, L.G.; CHXRMBkY, Recovery of noble metals by anion-exchar4ge resins from waste and. industrial solutions of electrolytic copper plants. Izv* vys.ucheb.zav.: toyet.set. 2 no.6:134-141 '59. OaRA 13:4) 1. Moskovskiy khiaiko-tekhnologich9str,4-, LLstltut. Kafodra tekhnologli plaStimes. (Copp'er industry-By-pproducts) (Ion exchange) (Precious metals-Metallura) 5(2) SOV/eO--32,-4-5./47. AUTHORS: Davankov. A.B... aufer, V.M. -------------- TITLE% - Or. the Problem of Elution of Precious Metals From Anionites After Adsorption (K voprosu ob-elyu-irovanii; blagcrodnykh, metallov iz anionitov posle adsorbtsi,i) PERIODICAL: Zhurnal prikladnoy khimii, 1959, Vol 32, Nr 4, PP 727-734 (USSR) ABSTRACT: The el-ation and relative resistance tc reducing agents of complex ions(AuCIZ, A,(CN)~) adsorbed on anionites is inves 'ti- gated here. The A,;,"" -4 ions adsorbed.on. a "E-011 anionite are easily red,.,cied to metal by hydrcquinone. They a ccumulate on the resin after several. sorption cycles in the quantity of ' more than 5 mg-equ. per gram of adsorbent., The Au(CN)2 ions are displaced by the solutions of sodium sulfide, hydrosirl-fide and kydrosulfite whithout reduction. This indicates the high resistance of cyanide anions to reduction and depc!~ition action of these agents. It is known that thiourea enters into- the reaotion of complexformation with metals, the sulfides of which are insoluble in water. The thiourea complexes are .. Card 1/2 easily decomposed in weakly alkaline solutions with the forma- SOV/80--32-4--5/47 On the Problem. of Eluti~-n of Prec:io,~.s Me"als From Anionites After Adsorption tion of sulfides. In is possible to extrac1t; 'l-he precious mietals Lompletely from resin adsorbents by this met-hod. 'The beL~t res-ilts are obtsined with a 2.0--sclution of 'l-hio-area -and a 13%-solut Lon of hydrochlor:~o acido Kurnakcv is -tuentioned in the text. There are tablee, I graph, ar.d 2 Sov-lat refererj~r_-3. ko SUBMITTED: September 1.9. 10:~- Card 2/2 -15-3610 75675 SOV/80-32-10-24/51 AUTHORS; Davankovj A B Oratynskaya, A. N., Laufer, V. M., Irp-5-skly, A G. TITLE: Deionization of Acid Albumin Hydrolysates by Anion- Exchange Resins PERIODICAL: Zhurnal prikladnoy khimii, 1959, Vol 32, Nr 10, pp 2269-2275 (USSR) ABSTRACT: Various domestic ion-exchange resins were tested for the separation of amino acids from the mineral acids residue in casein hydrolyzates. Slightly basic MMG-1 and AN-2F, medium basic N-0 and EDE-10P, and strongly basic AV-16 anion-exchange resins were investigated. EDE-10P and AN-2F resins gave the best results; the adsorption of Cl- and S04__ was complete, and that of amine nitrogen insignificant. The degree of deioniza- tion can be quickly determined by the pH value of the filtrate. When pH < 5.5., the deionization is practi- Card 1/2 cally 100%; at pH = 5.5 to 3.5, the Cl- content is Deionization of Acid Albumin Hydroly3ates by U Anion-Exchange Resins 7 f:j '75 0 SOV/80-32-lo-24/51 below 0.2%; pH4 3 shows a low degree of demineralization of the hydro.lyzate. The laboratory tests were repeated with practically identical results in a p.*'L.-'Lot installa- tion with stainless steel filterIng column of icn- exchange resin eapacity- are 5 ta-ble--i I flgure; and 5 Soviet references. SUBMITTED: July 21, 1958 Card 2/2 DAVANKQV,_Alaks&-f'r oriso-vich-, FEWHENKO, V., red,; VOLYNTSEVA, V., jakhn.red. [Magic grains] Volshebuys serna. Moskva, Izd-vo TaK VM3( ONolodaia gwardil:.," 1960j, 60 p. (MIU 13:8) (Ion axe-hangs) 5"%r5SO$ A 12J 0 AUTHORSg TITLE-. CAD Z101 'ZIDS 83701 Sllgo"601002100610061012 B015XBo64 Davankov, A. B., Zubakova, L. B. Synthesis and Investigation of Highmolecular Tertiary AminesAand Quaternary Ammonium Compounds on tha Basis of- the Copolymerslof 2-Methyl-5-vinyl Pyridine With Various "Interlacing" Agents PERIODICALa Vysokomolekulyarnyye soyedineniya, 1960, Vol~ 2, No. 06, PP- 884-890 THM An industrial method of producing 2-methyl-5-vinyl_p1rid~ne (Ref. -1) was developed in the Yaroslavskiy nauchno-issledo-Vatel's I institut monomerov (Yaroslavl' Scientific Resea-roh Institute of Monom-krs)v serving as a basis for producing important types of synthetic rubb~lr (Refs.. 2,3). The preseiit Investigation-deals with the me,%hanlsm and ',-.he conditions of a copolymerization of 2-methyl-5-vinyl pyridine with divinyl benzene (2-6%) and triethylene glycol dimethaorylia ester (2-20%)~- The high-molecular tertiary amines t)btained were t7ans!ovmed into insoiu'bla -.quaternary ammcnium bases by alkyla~,Ion. and the pxoduo+3 V~ Card 1/3 83?01 S/19 Synthesis and Investigation of Highmolecular . 0 (:,~~/,,N2/006/006/012 Tertiary Amines and Quaternary Ammonium Compounds B015YB064 on 4--he Basis o1 the Copolymers of 2-Methyl-5--vinyl Pyridine With Various "Interlacing" Agents obtained sZbJected to different physiao-chemical tests (anion exchange, ohemical stability, water absorption, swelling in organic solvents ets:1), On heatingi or irradiating 2--methyl-5 .__V4 nyl pyridin-a with 0~44 of ben?.Oyl peroxide only with a quartz lamp of the n-PK -2 (PRK-,2) typed the reattior products obtained were only soluble in organic solvents,, Copolymeriza- tion at 70-800C (end at 1000C) and a duration cf 4-5 h of 100 parts by weight of 2-methyl--5-v~.nyl pyridine and 4 parts by weight of di7inyl benzene besides 0-4 parts by weight of ~enzoyl peroxide in suspension resulted in a solid copolymer, insoluble in organic solvents, with weekly alkaline character, and anion exchanger properties (Table 1). k1kylaUon was carried out in the same cylindrical glass reaetion vessel as co- polymerization, with benzyl chloride; para-toluene sulphomethylate, ethyl iodide and mathyl iodide being used. Products of benzylation and methyla- tion with para-toluene sulfo acid methyl eatter had the highest capaoilty of exchange. The degree of alkylation rises with the reaction tine, An action of strong acid solutions (5 N and 9 N HNO 3P H2so 4) and lyss (1 N and 9 N HaOR) upon the anion exchangers in the form of tertieTy Card 2/3 83701 Syynthesis and Investigation of Highmolecular 5/190/60/002/006/006/012 Tertiary Amines arid quaternary Ammonium Compounds B015/3064 on the Basis of the Copolymers of 2-Methyl-5-vinyl Pyridine With Various "Interlacing" Agents amines was found to cause no reduction or their static and dynamic exchange capacity with respect to 0.1 N HC1 k-Ta,)Ie 2). The exchangers have a high absorptive power for phenol from ag.ieous solutions and a good exchange capacity for silver cyanide complexes~ There are 1 figure, 2 tables, and 9 references, 7 Soviet and 2 US. ASSOCIATION& Moskovskiy khimiko-tekhnologicheskiy institut im, D. I. Mendeleyeva (Moscow institute of Chemical Technology imeni D. I. MendeleyevT SUBMITTED& February 19, 1960 Card 3/3 S/190/ 60/002/009/020/023/XX B004/BO56 AUTHORS: Davankov, A. B., Zambrovskaya~ Ye. V. TITLE: Synthesis and Application of Polymers With Thiol-- and Thione Groups PERIODICAL: Vysokomolekulyarnyye soyedineniya, 1960, Vol. 2, No. 9, pp. 1330-1334 TEXT: The authors aimed at producing a cation exchanger containing SH- and =S groups and which, besides being used for analytical purposes, may also serve for the separation of metals, whose sulfides are difficultly soluble in water. For th.& synthesis of such an exchanger--resin, the authors used two methods. 1) The'ICArr(SDT) resin was obtained by the treatment of a chloromethylated copo-rYi-erof styreneland 2-4% divinyl benzene with thiourea. The SDT resin contained 11.3 -: 15.48% sulfur, and was hydrolyzed by means of 5% NaOH. The yield was 70--65%, referred to the initial chloro- methylated copolymer. The sorption properties of this resin are only little influenced by the pH. The dynamic exchange capacity, measured by means of 0.1 N AgN`0,, amounted to 2.7 - 2.8 mg-eqtdy'19. The regeneration was carried Card 1/3 Synthesis and Application of Polymers With S/190/60/002/009/020/023/XX Thiol- and Thione Groups 13000056 out by reducing the silver with NaHSO 3 or Na2so 3" When NaHSO3 ?ias used, no decrease of the absorption capacity occurred. In eight cycles of sorp- tion and regeneration, 238.7% Ag, calculated per weight of the resin, and/ or 22.1% mg-eqiAv/g referred to metal were adsorbed on the cation exchanger. 2) The'CHrjSNK) resin was obtained from a polymer containing amino styrene and 2%=iATinyl benzene by means of diazotizing with an excess of HNO 2 at 50C and treating the diazo compound with potassium ethylxanthogenate, The sulfur content of the resin was 5,16 - 6.10%. The dynamic exchange capaci- ty determined by means of AgNO 3 was 2.13 mg-equiv/g. Also in the case of this resin, NaHSO proved tobemore suited for regeneration. because the capacity did not aecrease to such an extent as when using the Na 2so The authors further investigate;ffH(TN) resin synthesized by A. B.,DavaKov and V. M. Laufer in the kaf-eTr-aplastmass (Chair of Plastics) of their institute. TN is a polycondensation product of thiourealmelamine and formaldehyde. The exchange capacity, which was T-eT-ermined _~ccordilg; to the above method, vas 2.70 - 4.44 mg-equi~/g, There are 3 tables and 6 references: 1 Soviet, 2 US, and 3 British, Card 2/3 F Synthesis and Application of PolymvrB With S119016010021009102010231XX Thiol- and Thione Groups B004/BO56 ASSOCIATION: Khimiko-tekhnologicheukiy institut im. D. I. Mendeleyeva (Institute of Chemical Tech.ology imeni D,, I. Idendeleyev) SUBMITTED: March 29, 1960 Card 3/3 DAVANKOV, A.B.; 1AUPER, V.M.; IOSILIVICH, A.I. New methods of sorption and desorption of silver by ionites in an electric field. Izv. vys. ucheb. zav.; tsvet. met. 3 no.4.61-88 ,60. (MIAA 13:9) 1. Moskovskiy khimiko-tekhnologicheskiy institut. Kafefra tekhnologii plastmass. (Silver) (Ion exchEtnge) (Zlectric fielde) 24738 S/080/60/033/007/024/024/XX 15'.-Noo D270/D304 AUTHOR: Davai-dcov, A.B. and Morovintseva,-11I.A. TITLE: Intragrannular chemical.transformatlons in copolymers' of viny-1 toluene irith divinyl benzene PE1110DICAL: Zhurnal priltl.~dnoy Ithimii, v. 33, no. 7, 1960, 1676- 1679 TEXT: The relationship between the structure of polymers and their, transformation, especially for the little-studied compounds of.vi' ny-; lene N-rith benzene and tolueneY has much practical and theoretical significance, so the authors investigated the c6polymerization of vinyl,toluene with divinyl benzene and the conversion of this'com- pound into a high-polymer amine. Copolymerization is effected-in -water in a glass cylinder fitted with a mechanical. paddle-mixerand reflux condenser. After heating at 75 - 85c)-for 5 - 6 hours on a water bath small c% anule 1i Mr g; (di am. 0.25 - 1 mm)-wl- ch assume a reddish color on washing a-nd drying, are separated'from the solutions... The relationship is shou-n,"L"irst -noted by Ye. B. Trostyanskaya et al Card 1/3 24738 S/080/60/033/007/624/024/,~Y. Ihtragranular chemical... D270/D304 (Re-'. 4: Khim. nauka i prom., 21 5, 593, 1957).of the numbet of lat-~ eral bonds in the molecular lattice of the copolymers to the swell- ing,of the granules in dioxane. Nitration is accomplished by cobl- ing a mixture o" the granules with HI'103 and H9S04 and then heating. it -on a water bath for *2'* .! 6 hours at 73' - 80U. Depending on the exact teraperature- and length of nitration, intermediate.-products with'a content of- 3.55 9.2976 N2 are obtained, possibly thro.ugh the following reaction: -CII-CHt- -cli-C112- IN .24. Not H3~ CO N02 The nitro groups are-subsequently changed into 'amine groups by'thei3~~ reduction with SnC12 in HCI at 1000. The granules thus synthesized' have a dark-bro~-m. or black color, the yield being 73 - 9.5% The .most complete nitra 'tion and reduction results *from an original ture containing the least divinyl benzene 2_475~ of the weight of Card 2/3 24736 S/080/60/033/007/024/024/XX Intragranular chemical... D270/D304 vinyl toluene. Unde these conditions the exchange capacity of the amino-resin is 5.5 and 5.9 mg equivs/g for 0.1N HC1 and 0 *5 H2SO4 respectively. The most stable granules, however, are prepared from copolymers containing the maximum amount of divinyl benzene - 8-10%-. In conclusion the authors stress the importance of the re- lationship between the nitration and reduction reactions and the number of lateral bonds in the molecular lattice of the studied copolymers during during their-conversion into amines. There are I figure, 2 tables and 4 references: 3 Soviet-bloc and 1 non-Soviet- bloc. The reference to the English-language publication reads as follows: H. Zentman, J. Chem. Soc., 982 (1950). SUBMITTED: December 7, 1959 Card 3/3 39U9 S/081/62/000/012/063/063 B150101 16"S t Do AUTHORS: Davankov, A. B., Zambrovskaya, Ye. V. TITLE: Synthesis and application of high molecular compound-s- containing thiols and thionic groups PERIODICAL: Referativny;f zhurnal. Khimiya, no. 12, 1962,- 669, abstract.' 12R89 (Bb."Isaled. v obi. prom. primeneniya sorbentov.11 M., AN SSSR, 1961, 27-~O) TEM. Sty-rene'copolymers with 2-4-/6,.divinyl benzene,.which contain sulfhydry- groups and are weakly acid cation exchange resins, are produced by the action of a solution of thiourea kin-whte~'or dioxane) on a ohloromethylated granular copolymer' (0.8:1)-with a 70-85~ yield ands a sulfur content of 11-3-15-3~. The exchange capacity from a 0.1 11 solution of AgNO after 8 sorption cycles is 22.1 milliequivalents/g; 3 !4' the Ag+ is reduced with a 10 NaRSO solution.. Ion exchange resin,- 3 containing functional SH groups, is obtained also by diazotizing a-co- polyimer of a7dnostyrene (11A N and divinyl benzene avollen in 2) Card 1/2 DAVANICOV, A.B.; ZJLNBROVSKAYA, Ye.V.; GERASHCHENKO, Z.V. Synthesis and study of sulfhydryl derivativen of polystyrene and its copolyners. Part 2. Vysokom.soed. 3 no.10:1468-1473 0 161. (MIRA 24:9) 1. Moskovskiy khimiko-tekhnologicheskiy institut imeni D.I. Medeleyeva. (Styrene polymers) (Mercapto compounds) DAVANKOV, A.B.; VITOL, O.A.; FAYNGOR, BA. Chemical transformatioris of gramilar copoly*rs of vinyltoluene with diviny-lbenzene and other "cross-linhing" agents. Part 1: Chloromethylation of vinyltoluene and divinylbenzene copolymers. Vysokom.soad. 3 no.10:1566-1571'0 161. (MIRA 14:9) 1. Moskovskiy khimiko-tekhnologicheskiy institut imeni D.I. Mendeleyeva. (Benzene) (Toluene) DAVANKOV, A.B.; LAUFER, V.M. Electrochemical. method of aorption knd desorption of-silver on ionites. Izv.-vys. ucheb. zav.; tsvet. met. 4 no.4:121-123 161. (MIRA 14:8) 1. Moskovskiy khimiko-tekhnologicheskiy institut, kafedra tekhriologii.plastwils. (Sorption) (Silver ions) (_. AVANKOV,__A_&-~-aBAKOVA,, L.B.; SPAMOVAp N.A. F(xtraction of nitrophenols from sqtLeom solutions by anion exchange resJns. Zhur. prikl. khim. 3tjnq.2s403-4(Y7 F 1619 (NIRA 3.412) (Phenols) on exbhange) * DAVANKOV, A.B.; ZUBAKOVA, L.B.j ANTONOVA, A.B. Preparation and chemical converaion of macro-molecular tertiary azineo into quaternary pyridine bases. Zhur. prikl. khim. 34 no*5:1310-1116 My 161, (KERA 16%8) (Amines) (Pyridine) DAVAM UO. A.B. ;APTOVA. T.A. GITERM Z'SH. !-r6ductioni-Triocesoes.ai 4on on ,,04dition ad oll*er 66h6ontrat iloirm-"Change ''ri., -0c.8:1852- Ag 161 14:8) (saver), w-ftduetion -eacti*), (idn exchange r~sius) DAVANKOV, A.B. (Moskva); LAUFER, V.M. (Moskva); GoRDIYEVSKIY, A.V. (Moskvai Storerooms of the Atlantic Ocean. Priroda .50 no.12:101-103 D ,61. (MIRA 14:12) (Atlantic Ocean--Uranium) (Ion exchange) DAVANKOV,-Aleksandr Borisovich,- FAYNBOYM, I.B., red.; RAKITIN, I.T., tekhn. r,,id,,*-'--,---'-',-, [Ion exchangerslionity. Floskvra, Izd-vo "Znanie,," 1962. 40 P. i'. (Novoe v zhizni.,.nauke,,ekhnik6. IV Seriia: Tekhnika, no.2A.) (HIRAL 15: 12) (Ion exchange resins) ~j S/149/62/000/002/007/008 Aoo6/Aloi AUTHORS: Da ankov,-A. B,,, Laufer, V. M., Azhazha, E. G., Gordiyevskiy, A. V., 2 .Kiryushov, V. AN. TITLE,: Experiences in extracting uranium and other elements from Atlantic Ocean water PERIODICAL: Izvestiya vysshikh uchebnykh zavedeniy, Tsvetnaya Metallurgiva, no. 2, 1962, 118-3.23 TEXT: Experiments of extracting various elements from Atlantic Ocean water were carried out in 1959,.during the sixth Atlantic expedition of the Marine Hydrophysical Institute of AS SSSR. Water from various parts of the Atlantic was filtered through an absorption column mounted on board the expedi- tion vessel. This vinylplastic column, 1,600 mm high with 63 mm internal diam- eter, was filled with 3.5 kg granulated H-0 anion-exchange resin in C1 form of 64% moisture. An amount of 59,189 liters of water was filtered through the column at an average rate of 40 1/hour. The qualitative and quantitative deter- mination of various elements in the resin was carried out by radiometric x-radiation, luminescent and polarographical analyses. The amount of uranium Card 1/2 S/149/62/000/002/007/008 Experiences in extracting uranium Aoo6/Aioi extracted on conversion to the tdal amount of air-dry H-O resin was 303 mg according to data of radiometriciLl analysis; 413 mg according to luminescent analysis, and 417 mg-'accordirijg;to polarograph~cal analysis. The pranium content in the Atlantic water calculz.~ ed from these data was: 5,12 . 10-13 g/1; (radio- metric analysis); 6,99 - 10- g/1 (luminescent analysis) and 7.04 10-6 g/1 (polarograghical analysis) or og conversion to normal sea water 4.7 10-6g/kg; 6.41 - io- g/kg and 6.47 ' 10- g/kg, respectively. Semi-quantitative spectro- scopical analysis of ash residue after burning the 0-H resin was used to estab- lish the presence of small amounts of silver, strontium, bismuth, zinc, copper,. manganese, iron, aluminum, silicon, calcium, magnesium, and sodium. The silver content in the absorbent was determined by cupellation of the ash residue after barning 200 g 0-H resin. An amount of 2.5 mg pure silver was then separated out which is 5.75 , 10-7 g per one liter of water. There are 4 tables and 13 references: 6 Soviet-bloc and 7 non-Soviet-bloc ASSOCIATIONS: Moskovskiy khimiko-tekhnologicheskiy institut (Moscow Chemical and Technological Institute); Kafedra tekhnologii plastmass (Depart- ment of the Technology of Plastics) SUBMITTED: February 25, 1,061 Car d 2/2 S/190/62/004/007/008/009 B119/B180 AUTHORS: Vitol, 0. A. TITLE: Chemical rearran-ements of granular copolymers of vinyl 0 toluene with divinyl benzene and other "crosslinking" agents. II. Chloromethylation of copolymers of vinyl toluene with ethylene p la' .,lycol and diethylene glycol di,-,Iethacry tes 1062, ZIERIODICAL: 'Tysokomolekulyarnyye soyedineniya, v. 4, no. 7, 1093-1097 TEXT: The authors studied the chloromethylation of vinyl toluene - ethylene glycol dimethacrylate and vinyl.toluene - diethylene glycol dimethacrylate in granular fo�m (grain size 0.5-1.0 mm) by means of monochloro methyl ether in the presence of SnCl4 and ZnC12 as catalysts. The content of ethylene glycol dimethacrylate and diethylene glycol dimethacrylate in the polymer was 2, 6, or 10~4. Reaction time and catalyst concentration wie~re varied in the experiments between 0.05 and 0.75 moles SnCI 4' or 0.1 and 0-75 moles ZnCl2 per base molecule of the copolymer. The following Card 1/2) S/190/62/004/007/008/009 Chemical rearrangements of granular B119/B180 optimum ::eaction conditions were found: reaction time 2-4 hr, dependirig on the co-,itent of crosslinking agent; 6-1051 crosslinking agent in the CoPol.ymer; 0.3 moles ZnCl2 per base molecule of copolymer in the ' reaction --aixture.' Copolymers containing 28.8~6 chlorine were obtained, corresponlimg to 158 chljoromethyl groups per 100 ben7ene nuclei. Reaction times-over 4 hr reduce an existing; chlorine content (formation of methylene bridges ivith separation of H01). Catalyst contents over 0.3 moles per base molecule of 7poly-mer cause a higher C1 content in the final product, but reduce its mechanical strength. There are 4 figures. The most important Engliah-language reference is: K. Pepper, H. Paisley, 11. Young, J. Chem. Soc.,-1953, 4097- ASSOCIATION: Moskovs 'kiy I-,himiko-tekhnologicheskiy institut im. D. 1. Islendeleyeva (11,0800%V Institute of Chemical Toohnology imeni D. 1. Mendeleyev) SUBBITTED: May 3, 1961 Card 2/2 DAVANK UFER, V.M.; AZHAZHA, E.G.; GORDIYEVSKIY, AN.; KIRYUSHOV,, V.N. Recovery of uranium and other elements from the water of the Atlantic Ocean. Izv. vys. ucheb. zav.; tsvet. met. 5 no.2:118- 123 162. (MIRA 15:3) 1. Moskovskiy khir-iiko-tekhnologicheskiy institut, kafedra tekhnolo ii plastmass. Rtlantic Ocean--Uranium) (Marine resources) BAKHRAXH, Ye.E.;--PA ,YANKQV-,-A,,B.; MARTEIRS, L.A.; LAUFER, V.M.; SOKOLOVA, N.M.; OBUKHOVA, Z.A.; FILIPPOVA, N.Ye. Cultivation of the plague microbe on media of acid casein hydrolysate demineralized using an ion-exchange resin. Zhur.mikrobiol.., epid. i immun. 33 no.3:51-55 Mr 162. (MIRA 15:2) 1. Iz Gosudarstvennogo nauc~no-issledovatollskogo instituta mikrobiologii i epidemiologii Yugo-Vostoka SSSR "Mikrob". (PASTEURIWA PESTIS) (CASEIN) (ION Examm RE-biNs) S/080/62/035/004 /006/022 D267/D301 AUTHORS: Davankov, A. B. , Lauf er, V. M. , Bortel E. --nd Tep- lyakov, M. M. -- TITLE: Sorption and subsequent desorption of yttlerbium and europium on granular ionites in an electric field PERIODICAL: Zhuriial prikladnoy Ichimii, v. 355, no. 4, 1962, 769-773 T--.;'XT: Thi successful application of redox processes for the con- centration and desorption of noble metals oil granular ionites in an electric field prompted the authors to use these processes in -the case of some lanthanides endowed with variable valency. Having cho- sen Yb and Bu as the elements to be tested, the authors intended first-to check the possibility of desorption in the electric field of tervalent cations adsorbed on ionites, and then to try to re- dUce them to divalent ions and utilize the low solubility of sul- phates for the purpose of concentration. Conditions have been stu- died of extracting and concentrating Bu and Yb from dilute solu- tions by means of'the cationite KJ-61,(KU-2), and a method has been Card 1/2 S/080/0'2/035/004/006//022 Sorption and subsequent D267/D301 developed -L:or achieving complete (> 955) desorption of Eu ions from the adsorbent and for obtaining concentrated solutions o-;L, EU by amalgamation. Yb did not, form amalgams with Hg. The method of desorption in the electrical field with the use of a Hg catChlode can be used to separate Eu from Yb and other rare-eartuh elements. Electrochemical desorption of Eu and Yb in the presence of E,,SO C- 4 solutions as electrolyte did not ensure a complete extr;-j-k;tion of uhese elements. There are 3 figures, 2 tables and 28 references: 18 Soviet-bloc and 10 non-Soviet-bloc. The 4 mopt recent references to the English-language publications read as follows: K. S. Spieg- ler, Techn. Rev., 100, 1953, 303; A. H. Creer, A. B. E~Indle-r and V. P. Tevmine, Industr. Engng. Chem., 1958, 166; R. S. S-Lamborg, J. Seidl and J. Rahm, Folymer Sci., 31, no. 122-123, 1955, 15-e-4; R. KU~,jj.jj, Toll exchange resins, Now York, 19~,8. SUBMITTED: April 13, 19061 Card 2/2 I VA.B~! Z'UBkKOVA., ,-PA &!JhQ L.B., ZVEGIMTSEVA, G.B. Complex formation with phenols arAl absorptive capacity of high molecullax woigbt d6riyatives of pyridine. Zhur.prikl. Iddm. 35 uo.r-It1I33-W5 My '62. (IMRA 15: 5) (F~,ridine) (Phenoa s) O."')n ox-~hange reeins) DAVANKOV LB_,-APMVA, T.A. Desorption-of silver and the regenezation of electron exchange resins by the electrochemical method. Zhur.prikl.khim. 35 no.1022171-2175 0 162# (MIRA 15:12) (Ion exchange resins) (Silver) (Electrochemistry) 0/190 3/005/002/013/024 X6 a I D10 102 AUTHORGV. Divalikov A'- 24. j:_,81Ato p. .19U.19 9 P.'M& TITLE: Hijbitol soul sr'dorivaif*fos 'Of. U-Nothvi styrene# 'I Bois* AM 00polymerol of-'a-liethyl styrene 5' MIZODiDAit. VysokoA6 ekdlyarnyye, it I '23 TEXT-j,',:.0J.r1cb Ahe *ion copolymerization ot arow yrenwvi U*411"yl'-Aen`ssioc'~ D agent Were .68 a rose linking in 'Ah f bj 1' no ion aopolmrbo-.- onck: 0 OAS a rolide Bug 0 ~. 'i so n 6 at io f '~Olyvinyl aloohol 1on4as. Q!* u -95 0. initlator, The yield wan'84 . - -1600 0 Using: 11itt as ` - - "ifi 44449; "S il . is C 0760 hkk )qi I ", the- - ni ix U14"and i -after 7 bris Afi or,: klobu Ar: gk"u1A7::'*sr"9 obtairiedi the,diemeter of Ai&-:*.' th o#pacity in b4h - it #,on Oilt The". illit~g~ ej 6 ohl 1,tv Oro A ARAG, d_1*6A66hio~iO' hy, ;h' r-de acid. with inoreigirg. 9 ore o- f croselink oOnt . t a on no, is from 152% with 4A DVYJ 0 4 r o ll. wMazeucM Sam /19OJ63/005/002/Oi3/024 -,'H 'ghmoledu st-t. B1 /B102 cqpoeniratio~. of Ahip -initiator 'and 'additiong -of :hid'sn'~-atceleratina offoot....Copoly" on'" 0 d." tbok.~`place also witho f ut lie hye dride 4~ 'hi: "iiO9604r,,ratio oi-,-c~-Oethy~, styrone and .'Mal-eio -h. t *as obtained Xati n r 0. &f ter3hra-.&V 60 Cj-~-*ith, oVrs,tio,-of...j:4~,. 0o2 bentoylperoiidej,the- 'at 75 d~'had thie 0.109- Mepo ~'!Ji~iyl~ioile "1 0' 1' 'rimi th iby-yMer: i1. "4;:~ Inst si!-oopo ~nme prop 0 -i II - -.,. . quolly,wi ftpus' copb ynera'are foi~xlids' There axe 1. fiore iaid t ASS001saf Ov, t "Oloji6hei iy ivistitit 1M. is-I-' lhlnikb~- ek, k 14, Ch4stical Tichuolqq Do LA".- %M- V2 i-19 SUP(ITTED 1 6 64_