SCIENTIFIC ABSTRACT FR:MAMEDOV, S. TO:MAMEDOV, S.M.

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CIA-RDP86-00513R001032000010-6
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December 31, 1967
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SCIENTIFIC ABSTR
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APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 s/2o4/~~/oo~/ou5/uah/uo7 Synthesis of new plastici.zer~+ from ... CU75/E13b distilled under l nun tlq. The fraction boiling l,etween 200 and 2,4Q �C (yield 7'G;'~a} con,~tituteci the new plasticizer named "F~NP~S " {ANAZ}. The plasticizer has negligible volatility (U.U~~-U.q~o at 1,o0 �C}, good light re:~istance, low freezing temperature (=40 to -~6~ �C} and gvod compatibility with plastics (does not sweat out from plastic films } and their solvents. It is insoluble in water, stable to heat and cold and non-poisonous . "ANAL" C 5-7`b } successfully replaces dibutylphtha late in collodion cotton and J butadiene-nitra~le rubber and castor oil in d+ermateen. It elso ~ replaces satisi'actorily tricresylphosphate in perchlorvinyl. ~, name is . There are 3 tables. ~-S~aC1ATI0Ns Institut nefte~ktiimicheskikh protsessov AN A25S~R {:institute of Petraer~emical Processes, AS Az.~SR} ~iUBMITTED : M~~rch 31, 1862 (;ard 2/2 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 s/zoo/6z/oozla~o5/oo6lotr7 ~a75/I";136 A-UTlIURS : Alemedoy, Shamkha 1 � .._ _._ ~ltzayev, A,S, ~ and Nixker, 1. L. 7'1~TLL: Synttaesi,nl of new plasticizers from keno rlal:~tithenic acids sane ~'~%RIUllICAL: Nef"tekhimiya, v. ~, no. 5, 1g62, 7ti~-792 TEXTt A search fo:r new methods of producing ~chea hi quality plasticizers led to the utilization of� naplythsnic e~cide as the raw -nateriai. Thp new plasticizers were ohl;ained ae f~pllaws: CH2C1 NaUOCR CH2O0CR + ~ + 2NaC;1 CH2C1 NaOUCR CH2000R wherQ R - naPhfihenic radical fractions of thE~ acids (keroseneonaphthQnic~~cXdeIndrviduaY 1]�0 to 14p �C _ acid value ~. r ~ 5~-60io fraction, acid value ^~ ~7"0_2t30) were neutralisedOwithagolin~ 140 to 160 �C SD'-100 �C. Dichloroethane was introduced at ,~ d ,NaOH at reaction being continued for 6-~S hours. The 70-lgip �C, the Card 1/2 products were J APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 ` �.v ~ ~ 1 ~ 1,.... .. ..o e w a ow. 1 ~{ ' a u.~. .t: 4' ~ f ~ ~ r~ter;ials of the Scientific Conference (Cont. ~ S r aVj'bx95 Yos~~~ ~3ynthenia of Some Organic Com~;ourds of Sulitir Wii;h Inseatiaidal and Aoarlridal Aotivity ' 344 ANALI"PICAI, CI~,idiS3"~ty ~gban~Y..~."~L., and T. R. l~itrzo eve. met~rio a~iethod of De erm n n ym Volunetrio-Iodlato- ploying Complex Compounds ofg' T~ j,entuChromiumina ~. 1 352 - ~ cx~rtzcAZ, ~rr~zrr~RIrra Melik-.Akhnaz `----~~~~+ ~s-~'� znveetigation of the Bleotrical t `'molting of pleas Name ~, 361 ' l~ and Y. Nizke o as loiter AHA3=yy""'-"~, and A. Rzayey. Syn~thesie 375 Card lE- f ~ ~~ ~~ . . ,~ APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 ,. i .. ..~ {~ r' i I Materials of th� Scientific Conference (Cont.) sov/61g5 i Vartanyan. s A., S. K, Pirenyan, and a~ g~khanyt-n. ~_,....--'' ~ Polymerization'ahd Reaction Mechanism of Acetylene in Vinyl Acetylene i 192 i Mamedov hamkhal. and A. Rza~ev. Investigation of Simple ,..,-,.,~,...,,. _.., ,-..._._w_ ~ ""~iTyaoT"E~at~xs and Their D�rlvativee: Synthesis of Simple ' "~ ~~~~ Ester Derivatives of Methylene Glycol 223 ~~ ~ I ~~, " Azatyat~~ V. D, Synthesis and Conversion of Cyclooato~tetraene 241 Lagidz~~~i.. Investigation of the Condensation Rea~at~ion of ""Ace'tie Esters of 1,3- and 1,4-Butanediola and Y-Aa~etylenia Glycols With Aromatic Hydrocarbons in the Presence oP O Anhydrous Aluminum Chloride 252 Sadykh�Zade. S. I. Direst and Organometallic Synthesis of ~ rganoailiaon Compounds With Functional Qroupa. (Inatitut ~--- khi~uii, Akademiya nauk Azerbaydzhanakoy SSR) 279 An industrial method oP synthesizing organoailiaon aompounda CPrd--~,,~1,~ ~n .~~Sg .., APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 . .~~ PHASE X BOOK L~aCPLOITATION SGV~61g5 Nauchnaya konferentaiya inatitutov khimii Akademiy nauk. Azerbayd- shanakoy, Armyanakoy i Qruzinskoy SSR. Yerevan, lg5r. Materia~.'~ nauchnoy konferentaii inatitutov khimli Akademiy nauk ,Azerbaydzhanakoy, Armyanakoy 1 Qzv ~inskoy SSR (Matar~lals of the Scientific Confarenee of the Chemical Institutes of the Acadeiniea of Soiences of the Azerbaydzhan, Armenian, and (3eorgi,an SSR) Yerevan, ~ Txd-vo AN Armyanskoy SSR, 1962. 3g6 p. 1100 copies printed. Sponsoring Agency: Akademiya nauk Armyanakoy SSR. Inatitut organ:L- cheskoy khimii. i I Reap. Ed.: L. Ye. Ter-Minaayan; Ed. of Publishing Hauae: A. t}. Slkuni; Tech. Ed.: (}. S. Sarkisyan. ,/. PURPOSE: This book is intended for chemists and chemical engineeres, . and may be useful to graduate students engaged in ch.emical.re- search. COYEAA4E: The book contains the results of reaearoh in~~hysio+sl, inorganic, organic, and analytical chemistry, and in ohemioal engineering, presented at the Scientific Cont'erenae lheld in ~, Yerevan, 20 through 23 November 1957. Three reports of parti- ~ aular interest are reviewed below. No personullties are mentioned. ' Referl:naes accompany individual articles. v ..T~~..~.....~_.~.__._,_... _ _.. ~ , ~.. .___..,.__~........,... ~a~.,.,,~ , APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 The New Plasticizer ANAZ ~'s%~~4 5~/44c/~7/Cr~7~'4, ~, B005~123 rvriilQ the glycol esters at' the naphthen~.c acids are distilled cuff at 184-210�, w:~ich are alr. lady the xeady product o The f:! rs't runnings are once mare ester1fied. The yield of the plastic:ize:r amounts to 74m80',~, compared to the used naphthenie acid mix~p lure. Prod.uctian costs of ANAZ are comparatively low. Tree n~>w Lalaatic:ize~r was tested in the dsrmatina~k].eyenorhnaya fabrilsa :Lm. No~;ina. ~Dsrmatin 4i1 Cloth ~Va, rks imeni No, ,~r~) in Kuntss~ra for thE3 production of dermatin and nitrolinoleum. Results s~~tis- :fy technical demands. &ioreover>' ANAZ ryas successfully used :in~ c~tead of tricrasylphos~phate as a plastiel.zer for enamr3ls of tha type P1~V, and instead of ricinus oil. far the production of nitro dyeel in aIPIa4 ~~tats D,.~s{~,,,�~n�d,~,'.,nni c, n ,;~,~�_~~____ i~earo_h_ 1ne~t~.tutuo~`.~~~rz,~,~.f~,~._....~.~,..~T.s~~X ~ It ws.s fo4uad �~~~~M'that coatings contain~.ng ANAZ can be coo~.ed aPP to ~>~G� without ,any loss cif stability. In NII rez~.novc~y promy~ahlennasti ~Sc;G~r :.._...., tifia ~~ss~~arch Institute of Rubbax Industry} good reeultc wire r~chievr~d with thee ngw plasticizer. T ere are 1 figures 1 table, c~nd b a~eferences, ~ of which are Soviet. Card 3~3 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 ~ry7~~ The New ~'lasti,>~.z+~r ANA?. ~/Obi 5~/a~~~/~i7 j~~7/�~, J~ooS ~T ~~ '100o fox ~ hours} era Compared to quali~.ieS of other popular ;~plaaticizelra. ANAZ is a ps,le yallr~wg nearly odorless oily l~.quid. ;E'or the production of 1 mol of this plasticizer one needs '1.1 mol off' the napYrthenic said mixtures 0.15 mal of aodi~rm l~ydroxide and Oat mal of dichlurnethanee For the esterifical:ion of the acid mixture distilled in vacuum9 it is neutralized at '120~160o with solid sodium hydroxide. The water produced is distilled off. The teuiparatuxe is thWri increas9d to 130�. Ait this temperature dichl.oz�aethane vapc?ra axQ led thxaugh the raix~- ture while mixing it tharougllly, The melted sodium salts of the rlaphthenic acids react witl~ the dichloroethane aceordir,~ to the ~ :following Schema: RCOONa C1CH2 RCOOCH2 ~ ~ -~--�~ 2 NaCl ~ ~ a RCOOPra C1C~i2 RCOOCH2 After csoolirr~� off the ~�aac~l.an mixtu.ze tc~ 50-40" wo~te;~ is r~dd~ad. ~~Che addition of water cs,ur3aa the pracipitatiora of sodium chJ.or;Lde ~.n crystalline faun which deposits readily. The eater is de�� czanted and distilled in a vacuum. With a pressure of 2 torr up Card 2/3 to 1704180�y the excess naphthenic acids are distilled off9 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 ~� "'~"`{~ _ _. C r n ~ ~~? 7th 7 ART$ORS : s/v64 ~~/OG1/07/G~7/C3~ ,w~Q~~ov . Slz . A,. r Rza~~ P ~ B005 B4 23 Riz cer � TITLE: The New Plastic AN',QZ I,' PERI~~DICAL; K:himicheski~ya promyek2lr'nnosto p ~ )59p N.r 7p PIS 580 �� 582 (USSR) AB$T].~ACT: I;n the pre,~ent paper the manufacture and. qualities of tl~ie nevi plasticizer ANAZ (abbrEa~riation far ~1,2d ,~zerbaydzhanslcoy SSR ( AS of th . e A~erba.ydzhanekaya SSR}}~ ~.re discusasd. Th~.c~ pla~ti~- c;f,zer whicY- ~7as for tliE9 first time produced ir. 19491950, con- s;iste of glycol sster~ of naphthanic acids and ie �apec~ally ,~ suitable for plasticizxn~ colloxylin. In the beginning the strong odor of thi9 planticizer ~ caused by the content of c:r�ude n~iphthez~ic acids -, pre;-ented its being used to a lamer exte�t. This odor can' ha~~vever9 be removed by a vacuum distillation I~f the naphthenic acid mixture used for synthesis, or of the rei~dy p~�oduct (Ref 3} In t bl , a a e thc~ mast important p~rysicochemica~l qualities of ANAZ (r~ialecular tiveight9 boiling point freezing , pointy ignit3.ori pointy d~09 refraction index at 200, sa~,vnifi ca�~ , Card 1/3 t3.on numberp content oY' volatile in~;xedienta when }ies,teci t'v APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 Inv~esti~tz.tion in the Field of rl~lcol Et::crs end `~ticir SCy~~-2~-f-~3%~r; Derivatives. 7i:XXIV. The Che;.lical Conversions of the y-Eth;;leie Chloride corresponding y-h~.lo~tTer~ ethers ~ p~eared as reaction productu; accord~.n~ to the I~~ar}:ovrii~~ov rule. ~.~}1c xe~,~;tiora z~~a.t}i t}it;: c~~,t:t TI'PLE: Tnvesti~ation in the Field of Gl;~col Et~~ers a,nd T~eir Deri~~;,tines (Issl~~dovaniye v obl~~ati prast~';h efirov Ulikolfi~~ i il.h ~r.~i~~- vodn,r~h} XXXIV. The Gher~ic~a.l Conversions of t~~e ^r-L~'th�'l~uU Chlori~'f:~�(XXXIV. 1~hit~ics~eslciLre prnvrwshciieniy, prosty?:la r~_~~.';Ic~r firov} ~'~):tIt~DICAL: Zhurril~,l obshchEy l;hir:~ii, 1~J- Fj`tl, Val 2f3, Pt:r ~, pp 1113 - 1C3f3 (USSF't} ADSTF~ACT; It tival~ p~' interest to tYte at~thars 'to investi,;~~~te the propea�ties of th~~ ei;her harnolo~,r~ of t~la e~11~ 1 alcohol (For;;lt~l~~ I1:) is~ dett~,i;l, ti~~hicYt lzc:a,s re-~Fl,inc.~d litt:la itive:.7ti;;.t;~tcad as i'ar rj.~: c~~z~ be ~~,u3~ecl fr~rn publ.a.c~>,tio:~.,. Orl thc~ ~,c~ti~a~~ of ri;~riz�a,.~;ori h}:t;l.i.rl+~~ on al:lyl ~31h~r(II)t~ Bauble ether corepound rerno.ir~e: pre �;rve~Y {~r,~.~ only the oxygen bride is dcstxoyed under t?'ie for~nxtion of un~- saturl~,ted (I1I} ~~,nd :~s.turatec~ (IV) hala;en deriv.:,tives of i,he hydrocarbons. The experiments: :showed, ho1~ever, ths.t over; in the cold (0~) HC1 and IInx can combine in the presence of ~~, c~~t Derivatives. XXXIIT. On Somme Cl.e~~l.c,:~l Convers7.ar.s of the p-Et~,;3. Br;~.^.~~c:~� of the Fatty Series . yield orb;�inamaE;nesiuln compolxr~cls (IIZ}, e~riich fora 1:4-~;lyco:l- ether (TVA tivith a~chlaric ether. This reaction process (see reaction i~che~ie~ points uo t~zc passibility of s, nee; s;;-ntuesis of glycol ether r~ith various allioxy ~roul~s in the positions 1,q.(IV). '1,3-dihalo~eri deriveti'~ives (V~ for,~~ on t};e actio:~ o:~' HBr or HJ on the yMet;;rl broridea This, e~ay six ~neti~ 1 ~ j-dih~.:to~en darivativE3s of fatty l~ydrocc.rbon;; t,~are sfnthetizerl (T rile:)-, I~11. above ~~eni;ioned ticonve,^siana make possibly the production of furthex cornpaunds on the ssrle basis., There s.re 1 t~~G,le snd 'j refere~lceF;, 4 of cihich are Soviet. ASS~~CIA'Z'TO2t: ~Azerbaydzhanskiy ~osuda~.~stvennyy pedf~~o itlesl;iy in titn.t (Azerb+~ydzhan Si; ate I'E~da,~;of~ic Tnstit~.ite7~ S17B1k~T`.~"!:'ED : t~pxil 1 ~ '~ X57 C~art~ 2~3 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 i AUTHORS: ~lamedov Sharnkhal, Zeynalov ~ a, K, SC~,'`7 __2,:~_ _1L~`~;,; .r t, f:=h TITLE: Inveati.,~s.�~ian in th4 ;~'1.~1t~ of Glycol Ft~~ers rind T:k~Esar Ac;r.~.v,;~t~.~ve (Iosladov,~niya v oblaati proat~kh afirc~v ~lilcaJ:o;~ i 1.i.k~ ~,r~;~;i:;�- vadnvkh} XXXIIIo On Some Cher~ical Conversions of t~.e y I~tl`-y:l Bromides of the Fc.tty 8eri~o (XXXITI~ 0 riekatoryl;.h ~ti.m~.+~k~esk~.kh prevrashcheniyakh prostykh y-brornefirov zhirnol,o rJ ~,.da) PERIODICAL: Zhurnal o'bshchey khimii, 1856, Vol 28, ter 7y pp 1831 ~- 1834 (USSR} ABSTRACT: Continuing an earlier peper (Ref 1} the authors crLrried out some little-known conversions of ~-ethyl bromide� The hydroiy_sis ex- periments of these ethers carried out in the presence of ti'a2C03 and CaG03(10-12 hours shovred that on this occe.sian HBr is split off under the formation of ethers of the homolo~;5 of ~~.llyl alcohol (II}a In a.ll these cases none of the incornp:~ete y�~,:~, ~~_ ethers to be expected, but only unsattxri~ted ethers r.;ef,ulted,. In the crlse of hery.tin~, tho y~~-r~tl~yl bran~a.der~ (x} :~ra.th r~lcr>holz.~t~Ea the HBr cleave,~;e to,kec~ only ?-~ houx�r~ �~r-d rzo etkierif'ict~,tion b~~t a forrnatian of allyl etY~era (IT) to,i~es place vrhic~~ corre,,pon~ls Card 1~3 to the ~Z~.:rkovnikov rule (Ref 1 } � The y�~ ethyl bromides easily APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE: 06/23/11: CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE: 06/23/11: CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE: 06/23/11: CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE: 06/23/11: CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE: 06/23/11: CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE: 06/23/'1'1: CIA-R~P86-005'13800'10320000'10-6 U93R~Organie Chem~stry� $yn,~hetic Organic Chernietry. labs Job t ReP ?~hur-Khi~a~ya~, Ito ~, ].957, 19051. Author M+~nadov Rhatc~shal, I~bdullayev A � ~na~t �~E. Title : 5yathe~ia of si~tpl� ~I~ycol Rthere . , o~ Dil~rc,o~q�'c~erivatives o;e Diwethyl Ethers of Tetraalkyl gubstitu~t~d EtY~ylene O~.ycoZe � Orig Pub: Azerb ~~tR e;lmler Altad- kheberleri, Txv. ~IJ ~1x8SR, ~,g56, I~Gr 5, 49-56. Abstract; T'he authors synthes1~substituted ilycolesPai'i behtype ethers c~P tetraa].ky a R2C(O(:~20R',~ (I) according to a previously described method (Tr. In�~akhimiyi AId Ax3gR, 196, 6) by the e,ct3on of C1CH OR' (II) on ~R~C (OMaX,~]~ (TTT} a product of the :Lnterac~tan aP R1~X with ethyl, ether aP ~luccinic acid (ether sa~ution, +~.me oP reaction ~+-~ Card : ].~2 E-2 APPROVED FOR RELEASE: 06/23/11: CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-005138001032000010-6 APPROVED FOR RELEASE= 06/23/1 1 = CIA-R~P86-00513800103200001 O-6 :~;~ ,~ ~ .....~,.......,....,M.,,..,.~,..~.,,,....~. -~-- ~ =~ 'Oi .~ }~� ~ 'brda+t+MOeft '� ~ ~ " ~~~ alit, #+~. ~ ~ y'1 ~: 1G11~r: ~#Awld; l Ni GBt , t#, t*..# , l'1~ #1f19~,TM-'i'ts . ~`twa. 4, Hb. i1, ; ~ ~ ~ ~ i ~ ~~} ryri>it !~ the ~ ~~~7i,~lt ~ �! i � ~ ~; i~~lr~+dln1 telly MNON In the y ~`*ri~. far Mt ha. at tJt)-d�, b. 1l18' dt~j p~,~j ~ ~ � ~' : K~ Lim. 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