SCIENTIFIC ABSTRACT KOZLOV, V.V. - KOZLOV,V.V.

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• Collection: Scientific Abstracts
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• Document Creation Date: January 3, 2017
• Document Release Date: July 31, 2000
• Sequence Number: 6
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

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Anthraquinione series. XI. Some a. and 0-mercury
derivatives of anthraquirione. V. %'. Kollov. Zhur.
Mkrhel K 4im. (I. (;,.m. Clietal.) Is'.-jj-.",)(Iq
j8); Cf.
J",kLjJy Ak.sd. Sai,k 57. 4117M117); CA. 43, 619c.--i
ack-firding it)
It4ttegay 411111 It-lilt-ir 30, ~111;~)Iji MINI fillet"j, was
Irrml4l "ills "it K. vullmy Hot n%idc Ill 'Of fill, W4 .
11cl
.1fid MI Ifil. yichlinK 76 5"; I-aRfAraquillotmediti.
-1-111141- ]1"'. ]'hi, Is 2 9.) ilk ,to I. W.C0. tr,.td
"ith IAI x. Of Lrmuc %itip stirring at 2-j-30' -)Yvr IS hors.,
litterr'l, al"I wa,hr'l fill h"t lit(Ill. r..'ve.53.5"~
Ill, 11,41% fr,,Ilj file Morale. %-)file thr ppl.
wi C%tfl. illi 11) g, 1-iling 1,11011 all'i '11111. (A tile CAI. fly
141 fill. 11'a xvl,,I,- K4,C ul";.
hbwple (Ill. yelf-iJi ism,lur, fit. This (11.5 K.)
v%ilh Ill 9
K011 alld Ill fill, 4 hr%. gave
Ill W; hrIp"u'le, a xrVy 111wil.
-11'1' ,I I '. *1 he 1y 1111 efolic.1
1, 'llini'le w
licl gives life ('rigmal chimple, ill. :J20-2" While curicti.
IGSO, at W give, t lir,j, ut! suffite. tievemp. 340', a j~wtfcr.
'T
woo
1 1-. ILA SITALLURDICAL LITERATURE CLASSIFIC4TIOM
! 1 A I a
_0
sac... %111411".
Q.W 44
L' slnos~ -1
$7 __T It
U 29 AV 0-0 IS rp it or it u a it fir 9 cf It It I
0 9 0e IS 0 0

ills-A. excel) t Ill Tile aci-I '111I.Ale rVII111"I
It hr%. %ith Koll-MeOll give, 97'; livdr,ni-le. The
-AWvc efilurifle 00 it.) ill -to) fill. 15 -16'; 'lleturl kel't ill a
I'melf Ve"64-1 3 1 1 1, it 15,;411.1 fill't"I int" i- xi~_ file
tll.,t
9.) M-1164 'Atilt stittillif 'kild 4-Ill.ic ('t Ill fill. NJ,-,C(l Aqt.1
7
11.15 K. U1 brinlie, let 11;kIld 1'.
. N, , aild dild. %%fill
N11,011. bAhmed I-v ~nrriujt 21 lin.. gives UIX)II
dilli. %illl .1 V416. water 07.71, Ji-1,10i1hrquipmPlitiNer.
'
r
y (111), xlrtyi,la. fit. L75-7' Minn Ac(M). 11 (1
:; a.).
:1,
,
t
fr 'I at WOO', was IrTelmad %Oth L ilmift AfnOll an,t 1, :1 K.
Cu bmaze in Lw fill. (Iry C,11,N; after sirring 4S hrs. at =00
there wal 01tained. 'm filtratilin. 7'.11 ; Iu. Ill

'a" a
M bui-A if, %-i,1,1 by -if.. -4 1 x. a$
-11
anthraquitume ill W fill. llr~4), at Ilki'twer:1 lirs., lc)llli%~
ago
"Y agItInfol 7.5 g. dry NaNf),, awl %1,,w addit. ,( tile dt.
g

a"a "llit, over 15 III)ill. Ill If,73 9. 119 vIII(Ate it$ I(M) U3. It,. o0
still file wIll. krIJI 1 5 Ills. at NO, Own ifit'i goo
'9111) fill. water, l")II(I'Arti by washillot %fill .11; 1 IN).. '
' 4r

Repetitiml of the last priorrilitre with 2-amim)unthr-.&qm- . e 0
nolle pvc 44-ax1hpaquismil-Impreary INV; ), a grryiIII, zo 0
lmorly 3ol. powder, tit.3115' ~ftom hot CIILN).
C'. %t. K~Aapoff
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I It t. A; ill 41 a N 's a V if A Z &- la 1, 1,
L-1 L_.1 14 L p 1, 1 t, Y I I U N l
tj
L tj
00 .
,
`00
.00
00 .2; Andwelivinesse emptivads. XZU. Adim of MUM41-
-00
00
ing Agents on I - and 2 -mercury -substituted consfiounds of -00
0o v. Kotloy. ZAmr. 06WA41 Kbits.
00 A (j. Gen. Chrin.) IS,-2rXll-21(Y21(l1.49); cf. C.A. 43,
-,ttlfjtr (2.5 K.) alive
2
1 hr. at 14110 will, M.8 X. to", Okulu give,, :PW~~ 211thfAtt"i- VUlloo4te (AlXtkit ~U:LWIAtii4l k1f
00 It now and M", K iW4,41"I by with Orurn EA~T
salting out with KCI; Mof olcum gives M% of the t3tlrf mixed %a 2. anti (rontc. 6 t i
00 1~-
as well as traces of the 1,5- still 1,94ijulte"kir; Sulf"n-
and 04% of the isomers, resp.), 9" a thrA( unlone n 1
4
~
' 00

00 - ation with 151r, olv~uiu at in the liresencr of a lit Ile mill anit. of 2.anthraquinunylm"
Ii
nidii
Cury sulti".

J .1 .
NXI L5 hr%. cave It*,'; alithriquillone anti 75% 1-41 - re4etion with cls(').11 x3ve llgClj, while th~ l[All-in.A
- ;.~* gs
ionic acid. as wrll a, Z-1141 'holif afill (isulated fly pptll. solid on extir. with ClIC1, x4ve about W
, unclulit"I ~o o
00 11 by diasotizrtl b,-nzi,line in the f.r?" of a 3.11t I CJI*(CO),- 14111K. obtained in pore stme afire wishmic with hot
CIll'sol-SW411,16, Twill. quantitatively ill acid f0)1".): Pholl; the c .. Ird PhOlf *)lit. give a ism.1) init. .1 :
0a isullonation fly C Stillf 3 firs. at 136* gives 76% antfura- axlkraqwoeoxylmrr(wy tkioride, infusible prisinl, which ~o a
so quinomr, with frati,li of file Z-vill/Osyl f1doride (sipi. by with Kcw~ in AcOll give fn '!N17, 5%
erysin.from pr1r. ether). K I -anthruflulturnesulfonale, Ifir CllClj ext. (we allovr) g.ivr 2vie, I -chl,po"nifivolui. :.041
00 anti 0", 2-sull'"Jair: excess COWhil givri anthra. jume anti a small atilt. ol.1-tj pilAtiqu laoswfsolfaisyl 4 Aloe i,k,
00 quinone, Mill;, m. 102, (frolo lWir. riliff). C, SI.
101~ I -nn t lira quinonesulfinot te. and 9% 2-1vomer. Sul. -00
foe%Ati~ -J 2.4 it. I I -C.11.(CO).C.11.1.119 by 11) S. !?11% -.04!
o0 11 nlrum 3 hr%. at 135* jrsve O.A4 x. K I -anthraquitiouriul-
foliate (from liP); thr insol. matter on extn. with ArOll goill
gave 0076 X. authraquinone and 1.6 X. I -anthraquitionyl-
loo :i mercury sulfate: similar reaction with CISCOI gives much
llgcll, a little .1 Ill 111141 25% too
d, vinx I-anthraquinoor.
quiplons, m. 1.W. the residuum he
..00

00
OtfUllUlt
tio 0
40 S

i
1
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U 11 0
09
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it 11 Is a N a 11 l
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0 0 0 0 0:0 0 0 0 0 0 0 0 0 0 0 0 0 & 0 0 9 All 0 0 0 0 0 0 0 0 0 0 0
0000 go 00 090 e 0 Pie 0 0 0-00 0 0 goo goo 6009 O,

!!-v~mlotrv, Anthraquirionedioulfbald- Jui,481:1~,~:
Acid
Chemistry
Hydrolysis
Hydrolysis of Anthraquiaoaedisulfonto Acids,= V.:V.'*,
Kozlov, Moscow Chemicotech Inst imeni D. I.
.Mendeleyer, 4 pp-
"Dok Ak Nauk SSSR". Vol L%I, No 2
Uperiments with disalfonle acids of aatbmquinone~~
their sodium salts in 80% salfario acid and In ~vi~:'
sealed tubes at 260o shoved.that their conver~ki~
.:xesembles-tbat of sulfonio acids of other aromatic~,',~;,
~6cm~ounda, bat requires more severe conditions
Jul, 48".1.11~1-1-~:~
Aathraquinonedioulfonic
Acid (Oontd)
Bither one or both sulfc, groups are subatitutbd
-,bydrogen' regerdless of their position (0~,cKl or.,-,
and merc=7 salts prcmote the, pr
d~.Cbnoantration of these salts and temperature coat'
eat of hydrolysis. In sealed tube salfo
are eabstituted by a hydraxyl. Hydrolysis of t~~
sodium, salts, especially in water, is 2 - 2.5 t
.slower. The closer the two salfo groups are to only
of the carbonyl groups, the slower to the hydro JLMIA
MI.
of one of them, and the more pronounced is the pre'.
6'MiLing direction of the process. Submitted
.28 Apr 48.
PAM

KOZLOV, V. V.
Kozlov, V. V. - 11",f7vtnty ycars from bw Lirtli of'
2in ber of Unc IP:H11 (All-JJnion Chemical Soc-lety) 1-men-i D. 1.
y mem
C) L)
,lendeleyev Vladimir 'L-'.f-k1haylovicL Rodi novfl Coo' s'nci- .o n2uc,,.
&Ienov Vsesoyi.,z. khim. o-va im. t-'r--ndnlt-yonva,
TSSUC 1y r~ . 1-4, with portr2it.
SO: U,-h630j 16 serA. 53, (Letopis 17hurnal Iny!-!. St;itey, ::o.
23) 1949).

CA
0 Serles. XIV. atel-Dilwhaii ;",
V. V. Kaslov and V. D. Swain. Zhai~
Mkrn (J. Cren, Chem.) 10. UH(IN9j, cf. c
C.A, 42. 0k; 4J, .38154.-I.5-AnthmquiuomdimfftxiyI
chloride (4 #.) (train the di-"It and PCIJ ground cArv-
fully with 8 mi. I" water at "DO and slowly treated with
4,11 g. NarS,9160 in 9 mi. IlsO, with the tomp. kept under
40', gave after 30 min. stirring, filtration, and scidilicatim
t
to Congo, red Oil It 110, the crude 1,3-dinifivic wid,
which after 2 repptas. from 10% N11.011 with 11C1 gave
X3.8% pure product. hygroscopic but M del*escent,
(arms a ktr4Ayd*ak an long standing in the air, sol. in 3 1,
pant Ifr0 at 20", slowly oxidized by 0.1 N XUW~,
readily t1trated with 0A N NaOff to methyl red gsdont,
its di-K, di-Na, di.(Njjj, di-Az, Afg,and rA nUssev sol.
inHj0; auto. of the add in Hv0, neutralization with 41L.- -
Off, and boiling off the excess N11# gave the following saki
by double decompri.: Ca (211,0), yellow plates (from
H,O), sol. 1:75 In 140 at 20% 1:24 at 100% M (211M.
yellow tates fmmHO).sW.l:l25wWl:M.reop..at,
2V smill 1004.! Pb 0140), Yellowish PWCI (from Ilso),
in". at 201. Very poorl Sol. at IW*; 04 0 yellow ncedles
(from StOll), insol.: ;a (511,0), yellow needles (from
ffvO),&W, 1:98at2f)'andl.30at Lou'. Addn.o(034g.
free "M In SD ml, 0. 1 N Na0H to 2.73 C. but IIgCI, in 8
Mi. 1110 Pvt 1.5 1. yellaw to.. CIO110".1111a, de-
camp. 340", yielding IfirCit ond ont1trequidatte. Ir8-
Anthraquirionedlittliony) chloMirt m, Z11.11", treated with
Na.8 as above gave after 30 min. at 40% filtration, Mid d
addn. of too mi *coned. HCI, 77.67c, crude 1,8-disaffink
", which is very difficult to purify because of Its high
MAY. in most org. "Veuts except hydrocarbons, Um prod.
uct Is a mo"ohydrute which does not loselfs0imoscivoover-
P at-pic; Its 4s.K, do-Nis,44MIJ.
ZDAja =S".y IUy!e IMA. I n 140; t he following saki . a.
mt& from the di-(Nll,) wit- Ca (411#0), yellow p4tes
from%Oot HIM), w4. ]: 12hat.21)"and 1: 115al IM" in
140; Ni ($H,10). scaks, (from UP or WOU), ". 1:3,11)
at 2DO and 1. 165 at lot)"; Pb (110).Plates (from 11.0 of
dil. AcOH). ad. 1:6W at :A)* and 1:273 at lou". Ca
(41110) tats, from 1140).Sol. I'Mat2l)".and 1:08al
1001, Ir. "u 1~
:1110 , plaitts (from If#0 or dd. AcOll), *A,-
1: W) at 20' and 1: 143 at V11; ZX (41110), crystals
(from 1110), VA. I:") at OD And 1:93 at I"U'. SIM.
ilattly, 1,4-ianthraquittonedisulfanyl chimidt IrciAttil with
SarS and kept 0.5 hr. at 40'. filtered, tvoled to V. suit
seidifird with coacd. IiCl, followed by vatu. with,fry IICI)
for 15-31) min. with cooling gave a granular 1.1-dualori,
ixcid. obtained an vacuum drying over Is'a0H in 9U% yield.
Very W. In 1110. 1111011, hffsCO, 50MtWhAt Sol, in
xylene. and almost insol. In hydrocarbons; moa of its-
Saltsam"Aull.0. Tbeacids ILse the followigm.ps..
XV. 1.3- ortlify.
COUWAIng unsymastric compounds of anthraquiam-
Nd. 745-5l.-1,5.t)iamino4nthraquinout (2Z3 S.)
ground with 2 mi. glycerol w4s mixed with 21) mi. coned.
MI, refluxed 30 tnia., coolvil to 4o4)". diazutized withvi
ml. 3D% filtered &fire 2 hn.. anit treated with 8.7
S. yellow fig oxide in 50 mt, Xl~'c 1ICI and W mt. firr);
the pink needles. filteml after 244 bet.. washed wah kv
water and EtOlf, and vacuum-ld"i represented a 47%
yield of 111CIt sAlt of the dianmium derm, CJ1ANOC'4-
11gi. decamp. 3W. %o1. in 1110, F.1011, MrC0. This
(8.7 S.) suspended In W ml, dry MerCo. tri-Atril with A
atirring, at 2"11 with 2,5 S. Cu brouse, lot stand o"r. ' I I
night, filtered the ppt. washed with hot EtOll, and that A
filtrate tr=t;i with rhareml unit coned. gave 9.8 g. crotle ,

product (m. I W-44*), purified by 441 bro.. con. with hot -
xyteme am cone". until it M. 230-441, (it was still impun) 1.
estn. for3 days with cold EtOll gave some 1.3-dick4woaa-
1049six"e, M. 243% while the residue contained fig and
Cl, treatment of the xvicne extP. "due with 3U'7* HSO~
12 Itts. smd washing w it It 110 and hot Etoll Pre 27% I'S.
(1). This (1j) S.) jms~
pended in 13 mi. KOII In 00 mi. dryl%ft-Olf and rtduuA 4
firs, gave a brown-bLack ppt- M.416,0 Of 1r5-Cj10G-
WcOll)jin-,ol. in the usuAlsolvrnts. This (01g.) added
10 10 mi. stirred ranol. iIrSO# at 0% filtered. and carr(ully
dihi. to 3 vols.,with 140 gave
114, *oL only n weak *from. I is recovered unchanged
I After 1.5-21 brs. in 5% oteum at 15'. but W/0 olcum gives
upon treatment with ice water 1111170 of a mized salt,
apparently at, witchaitsoan derm, deem 3W1-
11)1/0 okum 0 hr*. at NO gave 94 51,19' of the di-(&-WW
deriv., which Is olitalned In M.97,p':;4Id with 15% oku. 6
hr*. below room temp. The product (4 C.) treated
with 12 6. 10"a "Icum N) mitt. at 140* and =died out with
KCI ;avv 0.50 it. salf of a disulfanic acid. which yielded
1,5-dichloro"thraquinone m 241* fig dt-riv.
was recovered; 4.8 r. 21%~. ;iQm 140* pvt
.0.06 C. crude anthraquinone (in".) and the motiter
liquor im selling out gave 2 g. 41-K anthraquinonedisulfo.,
nate. yielding purr 14-dichloroanibratialmone (Identifying
the acid as the 1.5-isomer). Wt. 1,11-Mortm deriv-
aires of anthra.1"O (Unsymnietric). Aw. 804:
cf. DAniWY and Kai'mina. C.A. 43. 6370t.-Di-Na 1,11-
:utbroquintmirdivalfin4le (1.68 C.) in 1*1 ml. 0.1 NINsOft
7 ddid w51. IIjtC1pinWmI. hot IfA).boiW3hr*.,wItk
adda, of 0. 1 N NaOll until the mAn. I% clear Initiall v*
2A7 S. 1.S-6is(cA1oroxwrxrj) 1,6- R(7Z
which oil
and refluxed 6 firs. gave M.167o of the (A*oxymwr&6j
4rkA. greco-grey powAct. The Utter (0.5 X.) In
W . concd. IfjW$ mized at 0* and carefully diM.
with 3 vats, 110 gave 88% 1,,q-Cn11AU1jS04ff)*
on infusible solid; further sliln. of the filtrate Pre
some anthraquinove; the %Amc sulfac Is obtainct! in 7770
yield upon keeping the IISCI deriv.1a 101j'Ookum 6 hts. at
30-3* or in 181jIv olcum 6 hr%. in the cold (773% *M).
The sulfate (4 s.) treated with 12 c. I01% olcum at 1401
0.5 hr. gave O.:Vj X. I -anthragutinanesulf'onic wW (as the
chrysoldine saft). Anti OAS S. 1.8-anthraquinoncilisuffoole
acid (isolated asthe di-K salt by Salting out). while tstn. of
the residue with AcOlf gave 2 g. unreacied sulfate and 03
g. ot apparently I-rjo1fa4x1Araqaixa*y1a%ffcary sx1f4k (Aq-
sumed to be the 8-ivatner), brown, darkening at 323'
(from dil. AcOH). Sullottation with 25% oletun at 140'
1.0 hrs. gave OJA ff. 1 0,10 g.
dl-K ISAsulfonatc, aml 1.7t C. jjj.K I,8.dJsW(otute, the
insol. residar was frt* of fig alv] Pre Pore *11thraquinone
ondistn. Iftnce, the 1,84hiinterrurriadfate)girrse wWff
variety of prMucti on *ulfanation than the IvS-ivomer
because of grratcr thermal 6bility of the fig intcrooediste.
Ko"Ispoir

KOZLC)i.,, i. V. A 65/49T3v

KOZIDV. V V PA 67/49T55
USM/Chemletri". _Antbrao~one May 49
Mercury Compounds
nReoearch on the-Anthraquinone Series*..XVI, 1,8-
146rc'u'ry-'Containing Nonsymmetrical Compounds of
Anthraquii2one
V. V. Kozlov, D. D. Smolin, 51 PP
Mur ftshch Mde Vol XIX, No 5
.-Synthesizes hydkochloride of 1,8-anthraquinonyl-
~wcury.. and its severalderivatives, and determine@:
that the,principal product formed from the activity
of Oleum.oa this- compound'or the correspondililg 121a.7.
fate Is - 1~8.-dlsulfd acid of, anthrequinone. Sub-
Mitted 31 Jkm 489
Mimi 67/4ws5

KOZLOV, V.V.
Formation and hydrolycia of anthraquinonesulfoale acids. Yoprosy Anilino-
krasophnoy Khim., Trudy VIII Boveshchaniya KhIm. i Tekh. (Trans. 8th Aniline
Dye Conf.) 150, 167-80. (KIaA 4:4)
(CA 47 no.21:11172 '53)

Ih~ famposs to light of mikilitei tell its tit all is I lit a nil will v
of Its dtirivalives. V. tml k %I Sul
.1. Appli'd Ch'.. l2l hl."$ 4 J."'r'l
Lition); Zhk,. P,skldd. Khm 23, :117 24~ 11,1.'411 NII-Id, r
Likri lorlml. Imin pore, ImIkOwil millumpm w dy-
lit wilit-11 Ill.. '111hiall"., tv'J.11"Ible lof Lakt. Imiltall-I it.,
All"Vit"I tit mlly ow I"'ll A Oil, 1mg .'w to
dirt. fwtlIM4 to light. I'lle 1.11.... j"g F, I,'--- ill, ill, .11 ol-
lishing U%tuirvi to light: purptjrm,:k-arIxj,;yIic tci;l > litir.
llurin,l-sulfonic acill > pirworm > alizarin > t1iiiiiiz,am >
.4 lit hr~kjp I Io I %-I r I I., It V, Im% V.I. It hvi'l, I I, I ...... Nr tv
mad ptirl-tom -;I v.-
kill voill"11.4 N1.11to'l

KOZLOVjL V. V.; SMAHOV. B. 1.
Diethylaniline
Effect of glycerol and saccharose on the reaction rate of p-nitrobenzene diazonium
witb diethylaniline. Zhur.fiz.khim., 16, No. 6, 1952.
Monthly Liat of Fussian Accessionsp Library of Congress, November 1952. Unclassified.

KOZLOV, V. V.
Chemical. Societies
Activities of the D. I. Mendeleyev All-Union Chemical Society Vest. AN SSSR 22 No. 1, 1952
Monthly List of Russian Accessions Library of Congress, June 1952. UNCLASSIFIED.

KO~Lov,~V.V.; SmPANOV. B.I.
1" , I I
Influence of pyridine on the rate of coupling of -nitrobanzerLediazonium
chloride and diethylanilin'e. Zhur. Fiz. Khim. 2f. 592-7 '52. (MIRA 5:6)
(CA 47 no.20:10494 153)
1. D.I.Mendeleyev Ohem.-Tachnol. Inst.. Moscow.

KOZLOT. V.v.; STWPANOV, B.I.
Rate of coupling of p-nitrobanzenediasonium chloride with diethylaniline
inthe presence of quiholine. Zhur. Yiz. Khim. 26, 701-2 152. (MIaA 5:8)
(CA 47 no.20:10494 153)
1. MoAdeleyev C!"m.-Tachnol. Inst.. Moscow.

Mod cot afycwol and Sucirow on Sho into of c"Ohns P~
altrobansealtdianoolum cWwtde with d, toe % .
%', kinfilli #INI H. 1, SIT11,6110V (1). 1 A I !1V O."n -
--refurror - GIA. Ninw,?w /kill. fli. Kkl,m. .16. Sao 9
(111XII. it. gbj 7411. 111 I.Ir "ofto of thl,t wilplific it
&.11 land IS' . .. 7 :114, in :P%, jillm, And '.0 111 -f Id I
in Ihr I #1. 11 .,,,1 1 J.'a
m-A.A. Igiyvirrol. AM JJ. IA. ZM41. atki ~*.',I.Jl) X III I m
tht- I-r-we tit moVA. it IM, ai,4 ().WK tnot A. mwto~-
I hil" tuma h..Slwr greAl-t amifriat ills ett" C
J, J. Illum-r

KOZLOV, V.V.; STSPANOV. B.I.
*r,-,,t,-,--n
Rate of dia2otization of ?-anioldine. Zhur. Fiz. Xhim. 27, 3-5 '53.
(CA 47 n0.22;11918 '53) (mMA 6:2)
1. D.I.Mendeleyev Chem.-Technol. Inst.. Moscow.

KOZLOV, V.V.
In memory of Academician V.M.Rodionov. Ukr.khim.zhur. 20 no.5:
463-469 154. (MIRA 8: 1 )
(Rodionov, Vladimir Mikhailovich, 1878-1954)

KOZI,07, V.V.; BEWV, B.I.
-
Investigations in the anthraquinone series. Part 22. Hydrolysis
ofOC -antraquinony-lmercury sulfate. Zhur.of.khim. 25 no-3:565-571
Mr 155. (MLRA 8:7)
1. Institut, narodnogo khozvayatva imenii G.V. Plekhanova.
(Hydrolysis) (Mercury organic compounds) (Anthraquinone)

KOZL4DV, V.V.; YEGOROVA, A.A.
Study of the anthraquinone series. Part 23. Hydrolysis of anthra-
quinonesulfonic acid- CK # Zhur.ob.khim. 25 no.4:809-814 Ap 155
(MLRA 8.,;)
(Anthraquinoneaulfonic acid)

KOZLOV,V.V.
Investigntion of the anthraquinone series. Part 25, Hydrolysis of
1,8 disulfoacids of anthraquinone. Zhur.ob.khim.25 no.6:1206-1212
Je'55- (MLRA 8:12)
1. Institut, narodnogo khozyayetva SSSR.
(Anthraquinnnesulfonic Acid)

SPITSYN, V.I..; KAFUSTINSKIY, A.Y.; !~ doktor khimicheskikh nauk.
Hungarian chemical congress. Izv.AN SSSR.Otd.khlm.nauk no.5.*635-640
97 156. (KLR& 9:9)
l.Chlon-korrespondent AN SSSR (for Spitsyn, Kapustinakiy).
(Hangar,y--Chomistry-Congresses)

KOZLOV, Y.Y.
Yeallii, Vasillavich Shoxvin. Trudy Inst.ist.est.i takh. 12:285-311
156. (KM 9:12)
(Sharvin, Vasilii Vasillevich. 1870-1930)
1

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USSR/Organic Chemistry. Synthetic Organic Chemistry. E-2
Abs Jour: RoAl Zhur--Khimiya, No 6, 1957, igi64.
Author Kozlov V. V.
Inrt
Title Studics in the Antilrachinon Series. XXVI. Hydrolysis of
1,5--disulfonic acid of Anthrachinono.
Orig Pub: Zh. obshch. khimiyi, 1956, 26, No 9, 2617-2622
Abstract; By the hydrolysis of 1,5-disulfonic acid of anthrachinon
(I) and its Na- and K-salts in sealed tubcs (0.0025 molo
substance, 25 cc H2SO4 or ,vitor) all thuoretically pos-
j
siblo nroducta of the hydrolysis of 1, including the nro.-
ducts ~f tho substitution of S0311--zroup for TI were iso'-
latod. The ar-ount of I hydroli-od in 6 hours, by in-
creasing the temperature from 230 to 2600, in 80"13 112S04
is inorcaaad 2 times, in tinfis, in a 0.1',;-- and
95. to 98.2/o. Hydrolysis of I in water (2600, 6 houra)
Card 1 1/2
USSR/Organic Chemistry. synthetic Organic Chemistry. E-2
Abs Jour: Rof Zhur-Khimiya, iio 61 1957, 19164
proceeds to 97.2%. Thoroby arc formod Na-salt of 1-hydro-
xysulfonic acid-5 (11) 21'54 -slxlfol-lic a,,id 76.4,~~O; hydro-
xyanthrachinon anthrachinonc (III) 28.6"j. In
112SO2,, ,a 1.1011 aj ill wvtcry tha sulfo group is substitu-
ted in a higher dcmroo by It than by 011. Tilo Na and X-
0
salts of I do not hydrolize in water but in 112SOIj they
riydrolizL, vrith greater difficultYp than doca the free I.
t + 3 (2600,
Ilydrolysia of n-salt of I in a 70,' acirl
A
6 hours), 8T4 II and lZ6 III are formd. Tvic additiOll
of H~~04 lowers the totaponaturc, at -.;,ljcj1 tlic hydrolysis
occurs ani facilitates ' 10 formation of III. Report E(V
11
ace RzhKhim, 1956, 22435.
Card 2/2

. I I
,. I
s ~ I ..
I

*pv

K G 77- L- 6 1/ 1 V, t~ ,
~. !!!:Lv~ YAKOBSON' G.G.
Research on naphthalene series, Part 1,6t Conversion of 2-naphtolo-6-
--oulfonic acid salt Into 2-naphthol-7-oulfonic acid salts. Zhur.
ob.khim. 27 no-5:1156-1160 My' '57. (HLRA 1028)
(Naphtoloulfonte acid)

AUTHOR: Kozlov, V. V.
79-11-22/56
TITLE: InvestiCations in the Naphthalene Series (Issledovaniya v
naftalinovom ryadu).
XVII. On the Sensitivity to Light of the Aromatic
Selenium-Nitro-Compounds: 1-Ilitronaphthalene-5-,
1-bitronaphtlialene-2- and 1-nitronaphthalene-4-Selenic
Acids (XVII. 0 svetochuvstvitelfnosti aromaticheskikh
selensoderzhashchikh nitrosoyedineniy. 1 - nitronaftalin- 5
1 nitronaftalin- 2 i 1 nitronaftalin - 4 - selenistyye
kisloty).
PERIODICAL: Zhurnal Obshchey Khimii, 1957, Vol. 27, Nr 11, pp. 17011-3015
(USSR)
!,BSTRACT: In addition to his earlier investiCation the author
synthesized other isomeric nitroselenic acids of naphthalene.
He obtained them accordiriC to the z--cneral sdheme by
conversion of the diazotized isomeric nitronitphthalenes (see
chemical formula). The diazotization is best performed in an
acetic solution with dry nitrite, and the subsequent
oxidation of the solenium compound is best perf:)rmed by
boiling faith 201f nitric acid. 'rho aqueous zoliitions of the
Card 1/3 iv

InvestiCations in the Naphthalene Series. 79-11-22156
XVII. On the Sensitivity to LiVht of the Aromatic
Selenium-Nitro-Compounds: 1-Nitronaphthalelle-5-,
1-nitronaphthalene-2- and 1-nitrona-ohthalene-4-Selenic kcids
isomeric nitroselenic acids of naphthalene and the woolen
tissues soaked with then behave differently toward the
sunlight. The quantities of the sensitivity to liGht of the
isomeric nitroselenic acids of naphthalene, in comparison
with their sulfur-cont"ining analoeues, are to be seen from
the table. Thus isomeric selenic acids of nitronaphthalene
(1,2; 1,4; 1,5) and their salts were obtained. It was found
that the 1,5-nitroselenic acid of naphthalene is sensitive
to light, and that the 1,2-acid is sliGhtly sensitive. The
1,e~-nitroselenic acid of naphthalene shows a merked
sensitivity as compared to its sulfur-contr-ininE; sister
1-nitro-4-sulfinic acid of naphthalene.
There are 1 table, and --, references, all of which are Slavic.
Card 2/3

Investigations in the Naphthalene Series. 79-11-22/56
XVII. On the Sensitivity to Light of the Aromatic Selenium-
Nitro-Compounds: 1-Nitronaphthalece-5-i 1-nitronaphtlialene-2-
and 1-nitronaphthalene-4-Selenic Acids
ASSOCIATION: Institute of Economics imenj G. V. Plekhanov
(Institut narodno,,,o khozyaystva in. G. V. Plekhanova).
SUBMITTED: November 23, 1956
AVAILABLE: Library of ConCress
1. Aromatic selenium - Nitro-compounds - Light
sensitivity 1, 2. Light - Chemical effects
Card 3/3

-KQZIAA~-Uadimirj_on _ prof.; VOLIMVICH, B.I., akademik. red.;
r JUDInIvich,
BAIIKVITSM, A.L., n9d. lzd-va; POLTAXOTA, T.V., tekhn.red.
[History of chemical societies of the U.S.S.R.] Ocberki intorii
kbimicbeakikb obsbehestv SSSR. Pod red. S.I. Vollfkovicha.
Monk7a, Izd-vo Altad. nauk SSSR, 1958. 609 p. (MIRA 12:1)
(Chemical societies)

KOZLOV' V.V., Prof.
h Mendeleev Congress. .111im-nauk i prom.
3 n0-5:546-550 '58-
(MIRA 11:13.)
1. Glavmyy ucheW sekretarl Orgkomiteta VIII MendeleVevskogo
anyezda.
(Chemistry--Congresees)
5(2,3) SOV/153-58-6-9/22
AUTHORS.: Khrustaleva, V. N., Kozlov, V. V.
TITLE: Golorimetric Determination of Soluble Carbohydrates by Means
of Heteropolyacide (Kolorimetricheakoye opredelaniye
rastvorimykh uglevodov a pomoshchlyu geteropolikislot)
PERIODICAL: Izvestiya vysshikh uchebnykh zavedeniy. Khimiya i khimicheskaya
tekhnologiyap 1956, Nr 6, PP 47-53 (USSR)
ABSTRACT: According to the findings made by the authors, phospho-
molybdic acid can be employed, not only for the purposes
already known (Refs 1-3), but also, in a aulphuric acid
solution on short heating with carbohydrates, for the deter-
mination mentioned in the title, due to the fact that it
develops an intensively blue coloring (Ref 4). The paper
under consideration deals with the application of this re-
action to the purpose mentioned in the title. A recipe is
given. Although the interaction of the above acid takes place
even in the ence of H2so4 in the reaction medium, the
latter increases the coloring intensities of the solutions.
In this connection, heteropolyacid, via several processes,
is brought to a low molybdenum valency (Refs 5-10). The limita
Card 1/3 of the quantitative glucose determination are between 3 and

SOV/153-58-6-9/22
Colorimetric Determination of Soluble Carbohydrates by Moans of Heteropoly-
acids
42 g/liter (0.016-0.23 mol/liter). The sensitivity of this
reaction with regard to fructose (bluish-green coloring) is
between 0-3 and 15 9/1 (0.0016 - 0.083 mol/1). In jzlucose-
fructose solutions, the same coloring intensity emerges on
a concentration ratio of 10:1. The results are listed in
figure 1. On the heating with the acid concerned (in the ab-
sence of H 80 ) of diBaccharides, the coloring appears only
in qacchar9se! 112SO enhances this coloring. Ualtose and
lact,,se yield a coliring only in the presenae of H 2so4 (Fig 1).
The substitution of sulphuric acid by phosphoric acid enhances
the coloring in the glucose-fructose mixture also in the
presence of other carbohydrates. The coloring becomes purer,
and the reaction reasondiy sensitive. Table 1 shows the de-
pendenoe on the carbohydrate concentrations of the coloring
intensity of the solution. From this it can be seen that an
even increase of the optical dennity as a function of carbo-
hydrate concentration is characteristic of the sugar solutions
with a keto group, in particular of fructose and saccharose.
In this experiment there were no';iced differences in the re-
ducing power of the carbohydratel3. The sugars belonging to
Card 2/3 the aldoses or containing an a1do group shcwbut slight reduc-

SOV/153-58-6-9/22
Colorimetric Determination of Soluble Carbohydrates by Yeans of Heteropoly-
acids
tion under the given conditions. The concentration increase
of such carbohydrates but little increases the optical densities.
Figure 2 showo t~e data for keto Eugars from table 2 entered
into a coordinate system. Here, with regard to fructose, raf-
finose, and to lower concentrations of saccharose, all points
are arranged on a straight line. The curves concerned pass
through the coordinate origin. ThILS the solutions colored due
to the reaction in question obey Lambert-Buger-Beer's law. The
accuracy of the results can be increased by the use of an im-
proved apparatus. Table 2 shows the determination of the carbo-
hydrates in their mixtures. Table 3 presents determinations
of soluble carbohydrates in aqueous extracts from berries, fruit
and vegetables. There are 2 figures, 3 tables, and 12 references,
6 of which are Soviet.
ASSOCIATION: Kafedra organicheskoy khimii; Moskovskiy institut narodnogo
khozyaystva imeni G. V. Plekhanova (Chair of Organic Chemistry;
Moscow Institute of National Economy imeni G. V. Plekhanov)
SUBMITTED: December 9, 1957
Card 3/3

AUTHORS:
TITLE:
PERIODICAL:
ABSTRACT:
Card 1/2
Koz1ovT-*r-4,4_Solntseva, R. R. SOV/64-58-7-8/18
On the Hygroscopicity of Acid Azo Dyes
(0 gigroskopichnosti kislotnykh azckrasiteley)
Khimicheskaya promyshlennost', 1956, Nr 7, PP 416-420 (USSR)
The dependence of the moisture absorption of dyes as well as
their salts on 'the relative air-mo:;sture in the case of constant
temperature were investigated, and the function of this moisture
absorption versus time was determined. The maximum moisture
content observed during the experiment was regarded as the
equilibrium moisture of the dye. The determination of the
hygroscopicity was carried out according to the static
(or exsiocator) method (Ref 2). The quantity of th- equilibrium
moisture is a function of the relative air-moisturL and the
nature of the dye. The sorption iEiothermal lines have an S-shape
similar to those of capillary porous bodies (Ref 3). The
MniqflYre of the dye increases at constant temperature with the
increase of the relative air-humidity. This increase is
especially high at an air-humidity of more than 70%. At the same
relative air-humidity (e. 9. M/fj) the dyes acid red 2 C (15.7%),

On the Hygroscopicity of Acid Azo Dyes SOV/64-58-7-8/18
acid blood-red (12.9%), acid light red (11 3%) have the highest
equilibrium moisture, whereas acid orange ~8.6%) has the lowest
value. A comparison demonstrates that the order of
hygroscopicity of the dyes is almost the same as the order of
the solubility. However, no theoretical (Ref 5) dependence on
the structure of the dye could be found. The experimental
results on the moisture aboorption of sodium, potassium,
ammonium and calcium salts of the dyes show that (as in the
dyes themselves) the moisture for the most part is absorbed
within the first days. Fillers increase the hygroscopicity of
the dyes. There are 4 figures, 4 tables, and 6 Soviet references.
Card 2/2

KOZWV, V.V.
On the eve of the Right Mendeleev Congresn. Ukr.khim.zhur. 24 no.5:
690-%59L~ ' 58. (MIMA 12.- 1)
(Chemistx7--Congrasses)

' 74-27-6-6/6
;u1
AUTHORS: j
Khrustaleva, V. No, Kozl,?vq V. V. (Moscow)
11
-
TITLE: _
r
Color Reactions on Soluble Carbohydrates and Their Utiliza-
tion in Colorimetry (Tsvetnyye reaktsii na rastvorimyye
uglevody i ispollzovaniye ikh dlya kolorimetrii)
PERIODICAL: Uspekhi khimii, 1958, Vol 27, Nr 6, PP 752-784 (USSR)
ABSTRACT: The authorfixst stress the great importance of color re-
action in colorimetric analysis. In this connection an im-
portant part is played by carbohydrates because they absorb
no light in the visible part of the spectrum. In connecti *on
with this rnaction, which develoysaccording to the scheme.
carbohydrate-~oxidizing ag*ent--b-oxidation products of carbo-
hydrate + reduced reagent (colored substance ii Zolu-
tion), also indirect reaction in mentioned; it is further
pointed out that hitherto comparatively few papers have
been published on the colorimetry of soluble carbohydrates.
There follows an enumeration of methods, bared upon the
reaction of carbohydrates with various inorgun.c compounds.
Card 1/3 The following problems are discussed in this chapter; 1) The

V/74-27-6-6/6
Color Reactions on 3oluble Carbohydrates and Their Utilization in Colori-
metry
reaction of the reduction of alkaline copper oxide solutions.
2) The reaction of the reduction of acid copper oxide solu-
tions- 3) Reactions with potassium ferrocyanide. 4) Reaction
with chromium salts- 5) Reaction tith ammonium molybdate.
6) Reaction with heteropoly aciaa. 7) Reaction with sulphuric
acid. 8) Reaction with spl-n4- -cii. There follow the reac-
tions wit' cobalt nitrate 3odium nitroprusside,
hydrogen bromide, iron chloride, and caustic alkalis. In the
second chapter the authors give a survey of the methods based
upon the carbohydrate reactions with various organic compounds,
viz. reaction with picric acid, dinitrophenol, dinitrobenzene,
dinitrobenzoic acid, dinicrosalicylic acid, anthraquinone -
nitrosulfonic acid, phenol, thymol, guaicol, resorcinol, re-
sorcin-disulfoacid. orcin, pyrocatechin, floroglucina,
tt-naphtol, naphtol-sulfoacid, naphto-resorcinol, chromotropic
acid, dinitro-naphtol-sulfoacid, anthrone (or anthranone)p
methylamine, ethylenediamine, aniline, anisidine, berizidine,
diphenylamine, dibenzo-carbazole, thioglycol acid, urea
(carbarnide), diazourazyl as well as with triphenyltetrasol.
In conclusicn the authors z!,ay that the methods of the colori-
metric definition of certain (speciai) cerbohydrates require
Card 2/3 further elaboration (in their mixtures). There are 283 ref-

.7olor 'enclArm,.- o.-, "ol_,t jc! '.'hvir Aii.-I'%ation in '.'olori-
t
1. Carbohydrates--Spectrum 2. Colorimetry--Applications
3. Light--Absorption 4. Carbohydrates7-Test results
Card

AUTHORS Kozlov, V. V., Veselovnkuya, I. SOV/79-28-12-30/41
TITLE: Investigations of the 11aphth-alene Series (Issledovaniya v
naftalinovom ryadu) XVIII. On the Reaction Kinetics of P-
Tfa;)hthol With A(Incoun Am!,,ionia and Ar.,tamnium Sulfite Solution
(XVITI. 0 kinctike v--.ai.-,v),1oyotviya P-rviftola s vodnyml rast-
vora--.1i :~Mmialm i oullfita armoniya)
PERIODICAL: 'Zhurnal obshchey 1,himii, 19513, Vol 26, Tir 12,
pp 3333 - 3338 (USSR)
ABSTRACT: The amination reaction of naphthols -nith aqueovis solutions
of anirionin in the presencLI of salts of sulfurous acid is of
practical importance to the synthez;is of naphthylamines.
The chemiam of such a reaction was sugCe.,-tcd by 1". It. Vorozh-
t;-,ov (Ref 1) and further P--.plained by the authors according
to scheme(l). Naphthol can accordin,~ to this scheme, enter
reaction with sull'ites in the hitherto not isolulted keto as
well afj in the enol form producina an affili,,~tion product
correnponding to the keto form. The kinetic character of this
reaction process has not 1jeen described either. The results
obtained in the reaction of P-naphthol Gielting point 1220)
Card I with aqueous ammlonift in the prelence of ammmnium nulfite

Investig,,tions of the Naphthalene Serien. XVT11. On t*.,,c -)0Y/79-28-12-39/41
Roaction Kinetics of P-11aplithol With Aqueous Allmorlia and Ammonium Sulfite
Solution
are given below in detailed equations. The amination took
place in a rotating steel autoclr~ve at 150-1800. The rate
of the whole amination procegs is determined by the first
i.e. by tloe j%ite of t1he reaction of P.-naphthol with
(ITH HS0 Nallso The affiliation product
bisulfite 4 3 or I 3~.
of schei.ie (1) has a hi;-,h niobility and therefore keeps re-
, aith unf er the formation of naphthyl. amine.
acting .1
The tran of ormat ion velocity of P-naphthol depends on time
and teraperature; it io directly proportional to the product
of the concentrations of ii-iphthol and bisulfite, and is
independent of the coi-,centration of ammonia. The amina-tion
velocity can also) be caiiued to depend on the concentration
of the decreasing amrioniurn sulfite. In that case the reaction
rate is directly proportional to the product of the con-
centrations of P-naphthol and Fulfite, and is reversely pro.-
portional to the concentration of arimonia. Tables, figures
and eqaations illuntrate the role played by the concentration
Card 2/3 of wmr.-ionia Lind P-naVhthol, the amount of ammonium sulfite,

Invest igution8 of the llaphthalerie Series. XVIII. Ur: t"he SOV/79-26-12-39/41
Reaction Kinetics of P-Naphthol With Aqueous Ammonia and Ammonium Sulfite
Solution
time and temperature in the amination of P-naphthol. There
are 2 figures, 5 tables, and 5 references, 3 of which are
Soviet.
ASSOCIATION: Moskovskiy institut narodnogo khozyaygtva (Nioscow Institute
of Nati-aas-l Economy
SUBMITTED: August 22, 1957
Card 3/'~
1

50) SOV/153-2-3-12/29
'AUTHORS: Kozlov, V. V., Belov, B. I.
TITLE: Characteristic Features of Diazotization of Aminoanthraquinones
PERIODICAL Izvestiya vysshikh uchebnykh zavedeniy. Khimiya i khimicheakaya
tekhnologiya, 1959, Vol 2, Nr 39 PP 374-380 (USSR)
AB3TRACT: Various papers with remarks on the mentioned pecularities are
quoted at the beginning. In this connection Lukin (Ref 25) is
cited. The authors made comparative investigations on the be-
havior of isomeric mono- and diaminoanthraquinones in the dia-
zotization in various media. Diazotization is possible in hydro-
chloric and sulphuric solution; however, different conditions
are necessary for different aminoanthraquinones. The addition
of potassium bromide produces favorable effects in the diazoti-
zation of all aminoanthraquinones. The rate of diazotization
of the compounds investigated in hydrochloric and sulphurio
solutions decreases in the following seriest lt5-diaminoanthra-
quinone> 1,8-diaminoanthraquinone> oc-aminoanthraquinone> A-amino-
anthraquinone> 1,4-diaminoanthraquinone. The diazotization of
aminoanthraquinones is possible also in acetic solutions with
Card 1/3 sodium being used in dry state, without addition of a mineral

Characteristic Features of Diazotization of BOV/153-2-3-12/29
Aminoanthraquinones
acid. The diazotization takes place very rapidly in glacial
acetic acid, somewhat more slowly in 80 % acetic acid. A
temperature increase accelerates the diazotization in acetic
acid solution. In different aminoanthraquinones the complete-
ness of the reaction depends to a different degree on the
duration. The yields of the diazotization of five aminoanthra-
quinones in acetic acid at different concentrations are listed
in table 1. The authors also investigated the stability of the
formed diazo compounds. The results are shown in table 2. The
following series is obtained for the stability of the diazo
compounds of the aminoanthraquinones investigated:
~-> 1,5-> a-> 1,8-> 1,4. Table 3 shows the decomposition of
solutions of diazo-a-aminoanthraquinonein the case of different
duration of electric illumination with 500 watt. Table 4 gives
a survey on the decomposition of the acetic salts of the diazo-
tized aminoanthraquinones in the case of electrical illumina-
tion with 500 w :4 Table 5 shows characteristics of some double
salts of the diazotized aminoantliraquinones with sublimate.
The optimum diazotization conditions of Cc- and 9-aminoanthra-
Card 2/3 quinone and of 1,4-, 1,5-, and 1,8-diaminoanthraquinone are

Characteristic Features of Diazotization SOY/153-2-3-12/29
of Aminoanthraquinones
mentioned in this paper. Yu. V. Lyande and Ye. K. Malinina
participated in the investigations. There are 5 tables and
35 references, 10 of which are Soviet.
ASSOCIATIONj Moskovgkiy institut narodnogo khozyaystva imeni G. V. Plekha-
nova - Kafedra organicheakoy khimii (Moscow Institute of
Political Economy imeni G. V. Plekhanov - Chair of Organic
Chemistry
SUBMITTED: February 11, 1958
Card 3/3

5 (3)
AUTHORS: Kozlov V V Davydov, A. A. 30V/32-25-8-9/44
TITLE: On the Analytic Determination of the Sulfo Acids of the
Anthraquinone
PERIODICAL; Zavodekaya laboratoriya, 1959, Vol 25, Nr 6, pp 926 - 928
(USSR)
ABSTRACT: It was established that the chlorination reaction needed at
the preparation of chloro anthraquinone (I) and at the de-
termination of the sulfo acids of the anthraquinone (5A)
(which is based on the same principle), can be simplified.
The simplification is achieved by chlorination at the optimum
acid concentraiion which results in the instantaneousmixing
of the reagent at the beginning of the process instead of a
successive' addition of the chlorate. A considerable accelera-
tion of the'reaction results both for the a- and P-sulfo-sub-
stituted anthraquinones. The article contains the process of
analysis of the a-(SA) according to the chlorate method. The
chlorination of (SA) in a hydrochloric medium with simultane-
ous formation of chlorine (Refs 6-7) can also be effected
with other oxidation agents (K 2Cr 20 7' CrO3, KMn04 , etc). For
Card 1/2

On the Analytic Determination of the Sulfo Acids SOV/32-25-8-9/44
of the Anthraquinone
the,analysis of a-(SA) the following reagents are recommended:
1-30 - 1.31 g of the potassium salt of the a-(SA)t 100 ml of
HU (specific weight 1-19), 75 ml of 4n H 2s04, 2.0 g of
K2 Cr 207in 25 ml of water. The chlorination is rapid and uni-
form. Yield of a-M is 98-5 - 99.0% (Table of the reproduci-
bility of the analysis). At the analytiral chlorination of
other (BA) (P-, 1.:;-, and 1.8-' according to the last-mention-
ed method, the time of adding the K 2Cr 2 07-solution to the mix-
ture must be prolonged to 2 hours and the mixture has to be
boiled for from 2.5 to 3 h.-)urs. In the presence of sulfates
of alkali- and alkalin-7~ earth metals weighing more than 25%
of the weight of the (SA) lower results are obtained. In this
case the analysis must be conducted with the use of a mixture
of hydrochloric acid - sulfuri!~ acid. There are 1 table and
7 references, 5 of which are Soviet.
ASSOCIATION: Institut narodnogo khozyayatva im. G. V. Plekhanova (National
Economy Institute imeni G. V. Plekhanov)
Card 2/2

5(0)
AUTHORS: Kozlov, V. V., vollf"Ovich, 'CA is
TITLE: 8th hendeleyev ConCrebd on Goneral and Applied Chemiotry (From
March 16 to 23, 1959, in Moscow)
PERIODICAL: Uspekhi khimii, 1959P Vol 28, fir 12, PP 1399-1403 (USSR)
ABSTRACT: This is a report on the Congress quoted in the title. In the
preface, a short chronological survey of the preceding seven
Congresses is given. The Congress of Chemists, bearing in honor
of D. I. Hendeleyev his name, were started by the Russkoye
fiziko-khimicheskoye obshchestvo (Russian Physico-chemical
Society). On the 6th Congress held in Kharlkbv in 1932, the
Vsesoyuznoye khimicheekoye obshchestvo im. D. I. Mendeleyeva
fAll-Union Chemical Society imeni D. I. Mendeleyev) was estab-
x
lished. A. N. Bakh was elected chairman. The 6th Mendeleyev
Congress was convened by the All-Union Chemical Society imeni
D. I. Mendeleyev, the Academy of Sciences of the USSR, the
Ministerstvo khimicheskoy promychlennosti SSSR (Ministry of
Chemical Industry of the USSR) in cooperation with the Gosu-
darstvennyy Komitet Soveta Ministrov SSSR po khimii (State
-
Card 1/5 Committee of the Council of Ministers of the USSR for Chemictry)v~--

SOV/74-28-12-1/25
8th Mendeleyev Congress or General and Applied Chemistry (From March 16 to 23,
1959, in Hoscow)
and the Min:bsterstvo vysshego obrazovaniya SSSR (Ministry of
Higher Education of the IJSSR) (Ref 2). The Conference was or-
ganized under the auepioee of the Organization Committee
directly subordinated to the Prezidium i Otdeleniye khimiches-
kikh nauk AN SSSR (Presidium and Department of Chemical Sciences
of the AS USSR), Members of the Organization Committee were:
Academician A, No Nesmeyanov (chairman); Correspondir.g Member
ASVSSR N. Me Zhavoronkovj Doctor of Technical Sciences 1. P.
Losev, Academibian S. I, Vollfkovich (all vice-chairmen);
Doctor of Chemical Sciences V. Vo Kozlov (Scientific Chief
Secretary); Academician A. Yee Arbuzov; Academician B. A. Ar-
buzov; I. V. Belov of the VSNITO; Academician AS Ukrainskaya SSR
A. I. Brodskiy; Academician AS Ukrainskaya SSR P. P. Budnikov;
Academician A. P. VI,nogradov; Professor G. D. Vovchenko; Cor-
responding Member AS USSR No No Vorozhtsov; Doctor of Chemical
Sciences So V. Gorbachev; Corresponding Member AS USSR So No Da-
nilov; Academician Mo 14. Dubinin; Minister of High Education
USSR V. P. Yelyutin; V. A. Ivanov of TsK profsoyuza rabochikh
Card 2/5 khimicheskoy promyshlennosti (Central Committee of the Labor

I SOV/74-2e-12-1/25
8th Mendeleyev Congress on General and Applied Chemistry (From March 16 to 23,
1959, in Moscow)
Union of Workers of the Chemical Industry); Professor V. M. Ka-
kabadze; Doctor of Technical Sciences Y* S. Kiselev; Docent V. P.
Komarov; Academi&ian V. We Kondratlyev; Academician AS Lat-
viyakaya SSR L. K. Lepin'; Academician AS AzerbaydzhanskayA SSR
Yu. Go Mamedaliyev; Doctor of Chemical Sciences K. P. Mishchenko;
Corresponding Member AS USSR B. V. Nekrasov; Do P. Novikov of
the State Committee of the Council of Ministers of the USSR for
Chemistry; Doctor of Technical Sciences A. No Planovskiy;Dejuty
minister of Higher Education USSR M. A. Prokoflyev; Correspond-
ing Member AS'USSR 0. N. Reutov; Doctor of Technical Sciences
Z. A. Rogovin; A. Ya. Ryabenko of the State Planning Office of
the USSRI Academician N. No Semenovl-*Aoademician A. N. Terenin;
Vice-chairman of the State Committee of the Council of Ministers
for Chemistry S. M. Tikhomirov; Academician A# V. Topchiyev;
Doctor of Chemical Sciences K. V. Topchiyeva; Member of the Board
of the Ministry of Higher Education USSR N. So Torocheshnikov;
Vice-chairman of the State Committee of the Council of Ministers
Card 3/5 of the USSR for Chemistry G. V. Uvarav; Chairman of the State

SCT/74-28-12-1/25
8th Mandeleyev Congress on General and Applied Chemistry (From March 16 to 23Y
1959, in Noscow)
Committee of the Council of Ministers of the USSR for Chemistry
V. So Fedorov; Doctor of Chemical Sciences No A& Figurovskiy~
Academician A, No Frumkin; Academician I. I. Chernyayev;
Academician M. No Shemyakin; Academician AS Uzbekskaya SSR
So Yu. Yunusov. About 500 persons took an active part in the
preparation of the Congress. The 8th Mendeleyev Congress was
opened on March 16, 1959, in the hall of the Moskovskiy Gosudarst-
vennyy Universitet imeni M. V. Lomonosova (Moscow State Univer-
sity imeni M. V. Lomonosov) by the chairman of the Organization
Committee, Academician Ao No Nesmeyanov. He stated, among other
things, that the Academy of Sciences had considerably increased
since the last Congress was held. At presentp 12 chemical in-'---"
stitutee having a broader volume alone than the whole Academy
of 1934, belong to it. Chemical science comprises now, in ad-
dition, several dozens of industrial scientific research in-
stitutes# some hundreds of plant laboratories$ and about 80
chemical colleges and departments. Famous scientists of the
Soviet Union took an active part in all Mendeleyev Congresses.
Among these: N. No Beketov, N. A* Umov, V. I. VeTnadskiyj Do 9
Card 4/5 Konovalov, As Too Favorskiy, No S. Kurnakov, A. Too Persman, ~/

SOV/74-28-12-1/25
Sth Mendeleyev Congress on General and Applied Chemistry (From march 16 to 23,
1959, in Moscow)
IT. D. Zelinskiy, L. A. Chugayev, V. Ye. Tishchenko, D. N.
Pryanishnikov, A. 17. Bakh, P. P. Lazarev, V. G. Khlopin, A. A.
Baykov, S. I. Vavilov, N. A. Morozor,, 'N. A. Shilov, V. A.
Kistyakovekiy, and others. It was stated by the speaker that a
delegation of scientists and chemical engineers, members of
which were: A. N. Bakhq X. S. Kurnakovp N. D. Zelinskiy, E. V.
Britskep A. Ye. Poray-Koshits-, V. Ya. Kurbatov, and others,
had offered to cooperatewith the government on March 14, 1928.
For this reason, the Komitet po khimizatsii narodnago khozy-
aystva SSOR (Committee for the Realization of Progress
in Chemistry in the National Economy of the USSR) was estab-
lished. After the inaugural discourse was finished, the
Prezidium Tsentraltnogo Komiteta Kommunisticheekoy partii
Sovetskogo Soyuza (Presidium of the Central Committee of the
Communist Party of the Soviet Union) was, on suggestion of the
-chairman of the Organization Committee Professor I. P.
Losev, elected Honorary Presidium of the Congress. There ar
Card 5/5 1 table and 59 references, 58 of which are Soviet.

SOV/74-28-12-21'25
AUTHORS: Kozlov, V. V., Vollfkovich, S. 1.
TITLE: 6th Mendeleyev Congress. Plenary Mlectings
PERIODICAL: Unpekhi khimii, 10,59, Vol 28, Nr 12, PP 1403-106 (USSR)
ABSTRACT: This in 9 report on the plenary meetings hold on the 8th ','on-
deleyev Congress from March 16 to 23, 1959, in Moscow. From
the lectures held on the plenary meetinGs, the following ones
are mentioned: V. S. Fadorov,, Chairnan of the State Committee
of the Council of Ministers of the USSR for Chemistry (Ref 3);
V. A. Kargin (Ref 4); A. N. Nesmeyanov (Ref 5)i N- He Semenov
(Ref 6); V. I. Spitsyn (Ref 7); A. P. Vinogradov (Rof 8);
V. A. Engellgardt (Ref 9 *); A. V. Sokolov (Ref 10); Director
IIIIKhimmash V. D. Nikolayev (Ref 11); Ya. K. Syrkin (Ref 12)
and A. P. Aleksandrov-. All lectures were devoted to basic prob-
lems of modern chemistry and technoloGy as welIas to perspec-
tive problems of science. Plenary meetings were held with:
Academician A. N. Ilpsmeyanov, Professor 1. P. Losev, Academician
A. Ye. ILrbuzov, Academician S. I. Vollfkovich,Correspondinc:
Member AS USSR N. M. Zhavoronkov, Professor V. M. Kakabadze,
Card 1/2 Academician N. N. Semenov in the chair. The activity of the

8th Mendeleyev Congress. Plenary Meetings SOV/74-28-12-2/25.
sections took place from March 17 to 23P in the premises of
Moscow University, at the Institut biologicheakoy i meditsinskoy
khimii Akademii Meditsinskikh nauk SSSR (Institute of Biological
and Medical Chemistry of the Academy of Sciencesy USSR), and
at the Nauchnyy institut udobreniy i insektofungitsidov im.
Ya. V. Samoylova (Scientific Institute of Pertilizers and In
sect6-fungicides imeni Ya. V. Samoylov) (Ref 13)-
Card 2/2

v
5(0) BOY/74-28-12-3/25
AUTHORS: Koz1ov, V. V. Vollfkovich, S. I.
TITLE: ..8th. Mendeleyev Congress. Section of Inorganic Chemistry and
Technology
PERIODICAL: Uspekhi khimii, 1959, Vol 28, Nr 12, PP 106-1408 (USSR)
ABSTRACT: The Section of Inorganic Chemistry and Technology was working
under the guidance of Academician I. I. Chernyayev, of the
Deputiess Academician V. I. Spitsyn, Corresponding Member
AS USSR B. V. Feirasov, Scientific Secretary Candidate of
Chemical Sciences 0. N. Andrianova. Secretaries of the Section
weret Candidate,of Chemical Sciences T. N. Dymova, Candidate
of Chemical Sciences I. D. Kolli, Candidate of Chemical Siences
A. I. Lazareva, Ye. I. lonova, and V. T. Orlova. The meetings
were held witfis Academicians I. I. Chernyayev, A. A. Grinberg,
and I. V. Tananayev; Corresponding Member AS USSR I. A. Kazar-
novskiy, Corresponding Member AS USSR B. V. Rekrasov, Doctor
of Chemical Sciences I. N. Lepeshkov, Corresponding Member
AS USSR A. V. Novoselova, Professor G. A# Meyerson, Professor
0. Ye. Zvyaginteev in the chair. Lectures were held by: V. I*
Spitsyn, I. V? Yl~niiskiy, Ye. A. Ippolitova, I. A. Kazarnovskiyt
Card 1/2 A. V. Novoselova, K. N. Semenenko, A. I. Grigorlyev, S. Z. 9"Y
V-1Y

SOV/74-28-12-3/25
6th Mendeleyev Congress. Section of Inorganic Chemistry and Technology
karov, L. Go Bergg Vo I. Mikheyeva, N. N. Sirota, B. A. Berem~
zhanova, L. A. Borovskikh, Ya. Ye. Viltnyanskiy# S. I. Voll-
fkovich, No No PostnikovtA. A. Ionass, V. V. Illarionov, R. Ye.
Remen, Ye. P. Ozhigov, Go Ao Meyerson, V. M. Lekaye, A. Go Ka-
satkin, L. No Yelkin, Ye. Ya. Villnyanskiy, Ye. I. Savintsova,
L. A. Borovskikhp A. I* Teterevkovp L. So Byehikhina, 1. 1.
Chernyayev, L. A, Nazarova, V. So Orlova, A. A. Grinberg, Vo Go
TTonev, K. B. Yatsimirskiy, B. V. Ptitsyn, Do I. Vinogradovat
Ye. X.-Tekster# L, No Sheronov, Z. A. Shek, Ye. Ye. Kriasp
0. 1. Zakharoy-Nartaissov, 0. Ye. Zvyagintsev, V. I. Spitsyn,
Ye. A. Ippolitovap A* Pe Sokolov, V. M. Vdovenko, Ye. A. Smir-
nova, Do X. Suglobovj L, M, Gindin, P. I. Bobikov, E. F. Koub,
I. F. Koppp A. M. Rozen, No P. Ter-Oganesoyp H. I. Zagarskaya,
V. A. Kargin, R. P. Lastovokiy, T. A* Matveyeva, Yu. V. Shirokiy.
The lectures gave a survey of work carried out in the field of
inorganic chemistry. Now methods developed for the investigation
of inorganic systems and new procedures designed for the intro-
duction into industry were reported.
Card 2/2

5(0) SOV74-28-12-4/25
AUTHORS: Kozlov, V. V.p-Vollfkovich, S. I.
TITLE: Sth Mandeleyev Congress-Section of Organic Chemistry and
Technology
PERIODICAL: Uspekhi khimii, 1959, Vol 28, Nr 12, PP 1408-1415 (USSR)
ABSTRACT: The Section (Ref 15) i4as working under the cuidance of Academi-
cian B. A. Kazanskiy, Deputies: Corresponding Member AS USSR
P. A. Moshkin, Doctor of Chemical Sciences V. N. Belov,
Scientific Secretary: Candidate of Chemical Sciences B. I.
Stepanov. Activity of the Section took place, besides plenary
meetings, within the following 4 subsections: 1) Catalytic
Reactiona and Some General Problems of Organic Chemistry and
TechnoloGy (Head: Academioian B. A. Kazanskiyf Scientific
Secretary: I. V. Gostunskaya).-The ch6;irmen of this subsection
were: Professor D. V. Sokolovskiy, Academician AS Ukrainskaya SSR
Ye. A. Shilov, Corresponding Member Uzbekskaya SSR I. P. Tsuker-
vanik, Academician A. A Balandin, Academician AS Azerbaydzhan
SSR Yu. G. Mariedaliyev, Corresponding Member AS USSR A. D.
Petrov, Professor Yu. A. Gorint Professor B. V, Tronov. 2) Chem-
Card 1/6 istry and Technology of Aliphatic and Alicyclic Compounds (Heads
7

SOV/74-28-12-4/25
8th Mendeleyev Congress. Section of Organic Chemistry and Technology
Corresponding Member AS,USSR P. A. Moshkin, Scientific.Secretary:
L. N. Nokhapetyan). Chairmen: Corresponding Member AS USSR
P. A. Moshkinp Professor V. N. Belov, Corresponding Member
AS USSR S. N. Danilov, Corresponding Member AS USSR G..A. Razu-
vayev, Academician B..A..Arbuzov, Professor 1. Yao Postovskiyt
Professor T. I. Temnikovat Academician Azerbaydzhan SSR Yu. Go
Mamedaliyev- 3) Chemistry and Technology of Aromatic and Hetero-
cyclic Compounds (Headt Professor Yu* K. Yurlyevp Scientific
Secretary: I. I. Grandberg). Chairmen: Corresponding Member
AS USSR N. No Vorozhteov, Professor B. A. Poray-Koshits,
Professor A. A. Spryskov, Academician Ukrainskaya SSR A. I.-
Kiprianov,.Professor.V.,A. Izmaillskiy,.Professor Yu. K. Yurf-
yev,.Professor Vq V- Kozlov- 4) Chemistry and Technology of
Elemental Organic Compounds (Aead: Corresponding Member AS USSR
R. Kh. Preydlina, Scientific Seoretaryt Ye. I. Vaoillyeva).
Chairment Corresponding Member AS USSR R. Kh. Freydlina,
Corresponding Member AS USSR 0. A. Reutov, Academician M. I.
Kabachnik, Professor A. A. Petrov, Professor 0. Kh. Kamay, Cor-
responding Member AS USSR Do N. Kureanov, Corresponding Member
Card 2/6 AS USSR K. A. Kocheshkov. Lectures held by G. V. Uvarov, 11~

SOV/74-28-12-4/25
8th Mendeleyev Congress. Section of Organic Chemistry and Technology
Kh. K. Ingolld, G. A. Razuvayev,- M. I. Kabachnik, Ye. A. Shilov,
1. V. Smirnov-Zamkovt G. A. Piskovitina, V. G. Ostroverkhovt
D. F. Mironova, 0. F. Dvorko, A. A. Akhrem, A. V. Kamernitskiy,
L. D. Bergellson, L. P. Badenkov, Ye. I. Klabunovskiy, A. A.
Balandin, B. A. Kazanskiy, I. V. Gastunskaya, A. I. Leonova,
A. F. Plate, V. I. Stanko, A. A. Balandin, V. I. Spitsyn, N. P.
Dobrosel'skaya, I. Ye. Mikhaylenkop R. M. Flidq Yu. A. Gorint
I., K. Gorn, A, A. Balandin, M. L. Khidekell, V. V. Patrikey,-vl
Ye. G. Vollpoval A. V. Lyuter, E. M. Koganova, A. A. Vvedenskiy,
T. Ye. Shakhova, A. Ye. Panitkova, A. R. Perellman, I. M. Dol-~
gopol'skiy, A. L. Klebanskiy, Z. A. Dobler, M. Ya. Rubanik,
S. V. Zavgorodney, T. B. Gonsovskaya, L. S. Shvetsova, V. I.
Sidellnikovap V. G. Vakhtin, Ye. A. Vdovtsova, Yu. G. Mamedali-
yev, I. P. Tsukervanik, A. A. Balandinp I* Ro Konenko, A# A&
Tolstopyatovaj Ye. I. Karpeyskayat A. Ps Rudenko, A. A* Kuzl-
menko, Ya. L. Golldfarb, G. A. Rudakov, I. Ya. Postovskiy, N. N.
Vereshchagina, L. F.*Trefilova, E. I. Chertkova, I. A. Korshu-
nov, N. F. Novotorov, N. A. Pestunovich, V. N. Dubovskaya, M. R.
Leonov, V. V. Perekalin, K. B. Rall', G. D. Padva, Yu. V. Svet-
Card 3/6 kina, N. A. Dayev, V. M. Dashunin, R. Ya. Levina, V. R. Sk;var-

SOV/74-28-12-4/25
8th Mendeleyev Congress. Section of Organic Che~mistry and Technology
chenko, Yu. So Shabarov, A. L. Klebanskiy, V. F. Vosikp Yus As
Zhdanov, Is V. Machinakayat To A* Earkhash, R. Ya. Levina, V. K.
Daukshas, P. A. Kajkaris, No Ko Kochetkovp L. Is Kudryashov,
B. P. Gottikh, So No Danilov,'V. P. Kazimirova, A. A. Lopatenok,
To 1. Temnikova, B. A. Arbuzov, A. 1. Konovalova. M. No Shchu-
kinap V. Go Yashunskiy, No So Malinovskiy, A, Go Yudasinaj
M. B. Blinova, B. L. Moldavskiyj V. 0. Babel', R. Is Rudakova,
Mo Sh. Usmanovat V. Ko TByBkovsklyp P. A. Moshkint Ro 1. Kob-
zovag V* Vo Ndsmeloy, No M, Lebedevap No No Terpilovskiy, 0, Vo
Maminov, R. 6. Danyuohevokaya, N&,I. Kobozev, Yes No Yeremin,
M. P. Shostakovskiy, A. To Bogdanova, No As Nikolayev$,,. Ge. Kho
Kamay, V. V* Perekalina, go Go Tasnitskiyt Yes B. bollberg, Be A.
Sarkislyants, Too I.. Satanovskaya, A. P.-Zaytaev, Sh. B. Aliyevt
R. No Degtyarenkop P. A. Moshkin, L. Do Pertsevp So F. Kalinking
A. A. Pryanishnikovp P, Do Borisov, As No Vodzinskaya, I* A*
Grigorovf So 0. Skvortoorp V. P. S=arokov, Is P. Chistor,
So V. Chepigoq M, Yes Shpuntova, Yes Yes Shnayder, F. A..
.Vasyunina, Go So BaTysheva, Ye. So Grigoryan, M. Z Gera8lkina,
yalgovskaya
V. 1. Isagulyants, Lo N,,,-LavTishcheva, No Mo Przhi
Card 4/6 No No Vorozhtsov, A. A. Ponomarenko, Vo A. Izmaillskiyp P. As

SOV/74-28-12-4/25
8th Mendeleyev Congress, Section of Organic Chemistry and Technology
Solodkov, No A. Kitrasakiyp A. A. Spryakov, A. I. Kiprianov,
A, I. Tolmachev, No So Dokunikhing Lo Me Yegorovap Go So Lisen-
kova., B. A. Poray-Koshiisp'V. V Kozlovp Be L. Belov, Be I.
Stepanov, I. P. Gragerov, Me P. Ponomarchuk, M. Me Aleksankinp
A. F. Rekasheva, E. P. Darlyeva, B. A. deller, V. Vo Perekaliny
To A. Abramovich, I. P. Gragerov, B. I. Kissin, Do M. Ushakov,
pe K. Krutkovp Z. Is Krutikovaj Yee M Chernyshevap C, Me Bar-
kov,.N. K. Mashchinakayap Yu. No Sheynkert So A. Giller, L. A.
Favlova, E. Do Venus-Danilova, A. Fabritsy, Me No Shchukinap
K. M. Muravlyeva, Yu. K. Yurlyev, K. Yu. Novitskiy, M. I. Par-
berov, B. Po Ustavshchikovp A. M. Kutlin,, A. N. Ndsmeyanov,
0. A. Reutov, No So Kochetkova, No A. Vollkenau, V. Do Vill-
chevskayat V. Go Yashuns'kiy, V. F. Vasillyeva, R. Kh. Freydlinap
A. Be Belyavskiy, A. A. Petrovp Kh. V. Ballyan, Yee I* Vasill-
yeva, She A. Karapetyan, ~. A. Semenovp Re Go Petrova, V& N*
Kostt To To Sidorovap So T. Ioffe, Yu. N.,.Sheynker, To A.
Mastryukov, K. A. Kocheshkov, No Is Sheverdina, To V. Talalayeva,
Yee M. Panov, L. V. Abramovaf V. No Setkina, D. No Kursanovy
Yee V. Lykova, 1. P. Beletskayal 0. A. Reutov, Re Yee Mardal-
Card 5/6 eyshvili, E. Me Braynina, A. N. Nesmeyanov*p 0. V.,Nogina, Yu P
v

SOV/74-28-12-4/25
8th Mendeleyev Congres,so Section*of Organic Chemistry and Technology
I
Kudryavtsevt L.jo Zakharkinj I. Lo Knunyants, R. W. Sterlin,
A. N# Nesmeyanovt " 8# Isayeva, To P. Tolstaya, B. M, Mikhaylov,
P, M. Aronovicht Ai-l. Blokhinap T, K, Kozminskaya, To V.
Ko8troma, No So Fedotov, To A. Shohegoleva, V. F. Velichko,
To P. Tolstayap Av N; Nesmeyanovp L. S. Isayevat L. Go Makarovat
Oo A. Ptitsynaq 0* A, Reutovq As E& Shipbvp To Ya. Medved',
Ye. No Tsvetkovat Go Kh. Kamay, V. So Balabukht G. K. Kozlovaq
Ye, A* Mironoyal L#, Vq~ Tikhonova are mentioned, In the re-
solutions approved of J)y the Section, it was noted that lectures
and communications givd,evidence of-a noteworthy progress in
scientific research 'worX in the field of organi6 chemistry and
technology which are being performed-in the different republics
and towns-of the USSR. Ae Section calls the attention of
the Management of.the All"Union Chemical Society'~~menl Do Is
Mendgleyeva and the Offic4 of the Department of Chemical
Sciences of the AS USSR t6 the iecessity of driving ahead work
to establish a uniform no,m~nclature.of organic comboundso It
is necessary to publish, in\,.addition, a series of i~?nographs
on methods of synthesis for~elemental organic compo-Inds as
Card 6/6 well as a specialized textbo;k designed for this field.

5(0) SOV/74-28-12-r"~5
AUTHORS: Kozlovp V. Ve, Vollfkovichp S, I~
TITLEt Oth Mendeleyev Congress. Sootion-pf Analytical Chomistr,,,-

PERIODICALt Uspekhi khimii, 1959, Vol 28, Nr 112, pp 1415-1417 (USSR)
ABSTRACTs The Section of Analytical Chemistry (Ref 17) was working under
the guidance of: Corresponding Mem6r AS USSR 1. P. Alimarin,
Deputyi Doctor of Chemical Sciences'A. 1. Busev, Secretaries:
Z. 1. Podgayskayaq Go No BilimovichA Academician AS Ukrainskaya
SSR A, K4 Babkop Doctor of Chemical Sciences A, K. Ruzhenteeva,
Professor V~ I. Petrashen' , Doctor of Chemical Sciences V. I.
KuznetBov, Doctor of Chemical Scienc6s Yu. So Lyalikov, Doctor
of Physical and Mathematical Sciences A. K. Rusanovq Doctor-of
Chemical Sciences Do I. Ryabehikov, O~r~responding Member of the
Kazakhskaya SSR M& T# Kozlbvekiy, Pro~essor V. A. Nazarenko ~
presided over the Individual meetings ~of the Section.. Lectur~es
held by: I. P, Alimarin, I. V. Tananaypv, K. B, Yatsimirskiy)
Ye. F. Naryshkina, L. P4 Rayzman, Yu. 1. Klyachko, V. M. PesbL
kova, V. M& Bochkovaj V. I* Kuznetsov, Ae It Busev, Mo I*
Ivanyutin, A. - 1. - Portnov, R. P. LastovEkiy, Yu. I* Vaynshteyn,
Card 1/ 3 No M. Dyatlova, Vo Tee Temkina, 1e Do K%~lpakovaj V. A. Nazarerko,

BOV/74-26-12-5/25
8th Mendeleyev Congress. Section of Analytical Chemistry
Ye. A. Biryuk, G. Go ShitarIeva, La I. Kononenko, V. K. Kuz-
netsoval Xi-Ao. Tananayeva, V, A* Obolonchik# I* P. Alimarin,
Go No Bilimovich, Do I* Ryabehikov, A# No Yermakovt V. K.
Belyayeva* No Me Marov, A. K. Babko# V* F* Toropova, Z. Kh*
Shakhova,,Re K. Motorkina, So, A. Gavrilovap Ye. No Semenovskiy,,
A. I. Kokorin, No A. Polotebnova, E, Ye,..Vaynshteyn, Yu. Ii,
Belyayev,'V. V. Korolev, No So Poluektov', A* Go Karabash, Sh. I.
Payzulayev, L. I. Moseyev, Yus V. Morachevskiy, I. A. Stoly-
arovaq Me 0. Korshun, No E. Gellman, Ka-I* Glazova, No So
Shevelevaj-H.1I. LaTina, V. A. Klimovav Yee Go Bereznitskayaq
Ye. N. Plerkulova, So Ie Sinyakova, Zo; B. Rozhdestvenskaya,
1. A, Yar4moyt Ya. P. Gokhshteyn, Yu*' So Lyalikov, M. B. Bar-
din, Yu. So Temyanko, Io Do Panchenkb, No I* Udalltsova, P. No
Paley# Me Me Senyavinp No K. Galkinay A. M. Sorochan, X. Go
Polyanakiyp A* So Vernidub, V. 1. Petrashen', A. A. Zhukho-
vitskiy, Pe Mo-Turkelltaub are mentioned. The lectures dealt
with-chief trends in analytical chemistryt physical and physico-
chemical analytical methods, use of new organic reagents I
Card 2/3 organic elementary microanalysis, chromatographic analysial

SOV/74-28-12-5/25
Sth Mendeleyev Congress. Section of Analytical Chemistry
use of tagged atoms in analytical chemistry, VIII/
Card 3/3

5(0) SOV/74-25-12-6/25
AUTHORS: Kozlov, V. V., Vollfkovich, S. I.
TITLEt 8th Mendeleye.v Con.-Iress. Section of Physical Chemistry
PERIODICAL: Uspekhi khimii, 1959, Vol 28, Nr 12, PP 1417-1419 (USSR)
ABSTRACT; The Section of physical Chemistry (Ref 18) was working under
the guidance oft Academician V. N. Kondratlyev, Deputy: Cor-
responding Member AS USSR V. V. Voyevodskiy, Corresponding
Member AS USSR K. V. Chmutov, Corresponding'Member AS USSR
G. K. Boreskov, Scientific Secretary: Candidate of Chemical
Sciences V. Ya. Shlyapintokh, Secretaries: Candidate of
Chemical Sciences D. G* Knorre, Candidate of Chemical Sciences
V. I. Vedeneyev. The individual meetings of the Section were
held with Academibian Ve N. Kondratlyev, Academician A. A.
Balandin, Corresponding Member AS USSR V. V. Voyevodskiy,
Corresponding Member AS USSR K. V. Chmutov, Professor A. A.
Sokolovy Corresponding Member AS USSR N. M. Emanuel', Cor-
responding Member AS USSR G. K. Boreskov, Professor H. B.
Neyman, Corresponding Member AS USSR Ya. I. Gerasimov, Profes-
sor D. N. Frank-Kamenetskiy, Professor K. P. Mishchenko, Cor-
1
Card 1/3 responding Member AS USSR S. Z. RoGinskiy in the chair. Ac- L1

5th Mendeleyev Congress. Section of Physical Chemistry
SOV/74-213-12-6/25
tivit,*..of the Section took place in 3 subsections: Kinetics
of Chemical Reactions; Structure of the Matter; Catalysis and
Adsorption. LectureB held byt V. 11. Kondratlyevq V. V. Voye-
vbdskiy, N. M. Emanuel', M. B. Neyman, K. K. Andreyev, It'. N.
Semenov, A. B. Nalbandyan, L. V. Karmilova, N. S. Yeni-kolopyan,
No V. Topchiyev, I. V. Patsevich, V. Ya. Shtern, A. P. Ballod,
To V. Fedorova, S. I. Molchanova, Ya. B. Zelldovich, A. So
Sokolik, L. A. Lovachev, A. N. Terenin, F. I. Vilesov, M. V.
Vollkenshteyn, P. P. Shorygin, Z. S. Yegorova, I. V. Aleksand-
rov, N. D. Sokolov, So A. AlItshuller, K. A. Valiyev, A. I.
Rivkind, B. M. Kozyrev, P. 0. Tishkov, V. I. Avvakumov, L. A.
Blyumenfelld, S. Ya. Prenkell, S. Ye. Brealer, A. I. Kitay-
gorodskiy) Z. V. Zvonkova, V. V. Tarasovy V. V, Voyevodskiy,
A. V. Storonkin, A. Go Morachevskiy, M. P. Susarevp M. M.
Shullts, M. I. Usanovich, S. S. Urazovskiyq Do So Taiklis,
Ya. I. Turlyanp M. M. Dubinin, V. P. Kiselev, Ko G. Krasill-
nikov, A. V. Kiselev, A. Ya. Korolev, K. Do Shcherbakova, S. Z.
Roginskiy, K. G. Boreskov, D. V. Sokollskiy, Ya. B. Gorokho-
vatskiy, A. A. Balandin, V. E. Vaoserberg, M. P. Maksimova,
Card 2/3 To V. Georgiyevskaya, V. Kh. Matyubhehko, A. A. Tolstopyatoval,

6th Con~;rccs. soction of PhyE;ical Chemistry
SOV/74-26-12-6/25
i-1. V. rolyakovq V, V. I-hallf Z. Z, Vysotskiy, A. M. Rubinshteynq
T. Rusov, A. A. Slinkin, V. I. Yakerson are mentionea. In
a resolution taken by the Section, it was noted that progress
in theoretical and experimental investigations in the field of
tonochemical reaction~jis stayinE; somewhat behind the general
level of work in the field of chemical kinetics. Too little
physical and physice-chemical methods are being used. It would
be more appropriate to establish now laboratories and a central
head office.
Card 3/3

5(0) SOV/74-28-12-8/25
AUTHORS: Kozlov, V. V., Vollfkoviohl 8, 1.
TITLE: 8th Mendeleyev Congress. Section of Chemistry and Technology
-
of Polymeri
PERIODICAL: Uspekhi khimii, 1959, Vol 28, Nr 12) PP 1422-1423 (USSR)

ABSTRACT: The Section of Chemistry and Technology of (Refs 21,
48-4904) was working under the guidance of: Academician V. A.
Kargin; Deputy: Professor Z. A. Rogovin; Sciontific Scorotaryt
Candidate of Chemical Sciences Yu. M. Malinskiy. Academitian
V. A. Kargin, Academibian S. S. Xedvedev, Professor Z. A. Ro-
goving Professor N. N. Shoryginal Professor G. L. Slonimokiy,
Corresponding Member AS USSR V. V. Korschak presided over the
individual meetings-of the Section. Lectures held by: I. P. Lo-
sev,.L. A. Datakevich, K. 1). Petrov, 0. K. Gosteva, V. I. Pu-
khovap K. A. Andrianov, A. A. Zhdanov, 0. Ya. Pedotova, N. I.
Skripohenko, I. P. Losev, G. 1. Kud)~yavtsev, Ye. A. Vasillyeva-
Sokolova, M. A* Zharkova, S. N. Ushakov, V. A. Kargin, P. V.
Kozlov, N. A..Plate,.I. I. Konoreva, Ye. V. Kuznetsov, S. S.
Spasskiy, A. V. Tokarev, M. A. Mikhaylov, A. I. Tarasov, T
Card 1/2 Molchanov, M. Ye. Mat1kov, V. V. Korshak, S. L. Sosin, III . ~.v

SOV/74-28-12-8/25
,k- llenOeleyev Congress. Section of Chemistry and Technology of Polymers
Chistyakovaj 1-1. S. Akutint Bo H. Kovarskaya, L. I. Goluberelcovat
K. N. Vlasova, S. P. Kalinina, No Ya, Farlashkovich, V. N.
Kotrelevj Z. No Tarasova# No Ya. Kaplunov, No A. Klauzon, B. A.
Dogadkint V. L. Karpovt V. K. Lyubeznikov, M. Go Zaripovaj
Yu. L. Margolinal B. A. Dogadkin, 0. No Belyatakayao N. 5.
Felldshteyn, 1. 1. Ey-tingon, Z. 11. Nudellman, A. So Novikov,
K. F. Kaluzhenina, N. P. Zinchenko, Go No Buyko, No M. Arenzon,
A. I. Tumanova, V. A. Kargin, A. So Novikov, F. A. GaIii-Ogly,
Go M. Bartenev, N. V. Zakharenko, F. S. Tolstukhina, A. S. Kuzl-
minskiy, T. G. De6;teva, A. A. Vanoheydt, No N. Kuznotsova, F. To
Shostak, Z. A. Rogovin, V. A. Derevitakaya, R. V. Mikhaylov,
Z. 0. Serebryakova, No No Shorygina, A. A. Chuksanova, A. F.
Semechkina, L. L. Sergeyeva, A. B. Fakshver, L. V. Kozlov,
V. I. Selikhova, G. S. Markova, V. A. Kargin, V. A# Karc-in, V. A.
Kabanov, I. Yu. I,,,-.rchenko, V. Ye. Gull are mentioned.
Card 2/2

5(0) SOV/74-28-12-11/25
AUTHORS: Kozlov, V. Vol Vollfkovioh, So I@
TITLE: 8th Mendeleyev Congress. Section of Chemistry and Chemical
Technology of Fuels ---
PERIODICAL: Uspekhi khimii, 19591 Vol 28, Nr 12, pp 1426-1428 (USSR)
ABSTRACT: The Section of Chemistry and Chemical Technology of Fuels
(Ref 24) was working under the guidance of: Corresponding
Member AS USSR N. I. Shuykin; Deputy: Corresponding Member
AS USSR No M. Karavayev; Scientific Secretary: M. A. Ryashen-
tseva. The activity of the Section was divided into two topics:
Petroleum Chemistryq and Coal Chemistry. Corresponding Member
AS USSR No I. Shuykin, Corresponding Member AS USSR No M. Ka-
ravayev, Doctor of Chemical Sciences N. V. Lavrov, Doctor of
Chemical Sciences N. G. Titov, Corresponding Member AS USSR
A. Do Petrov, Candidate of Chemical Sciences S. I. Khromovp
Professor A. F. Plate, Doctor of Chemical Sciences So R. Ser-
giyenko, Professor No I. Chernozhukov, Candidate of Technical
Sciences V. P. Sukhanov presided over the individual meetings
of the Section. Lectures held by: V. P. Sukhanov, No M. Ka-
Card 1/2 ravayev, No V. Lavrovp H. I. Shuykinj N. Go Bekauri# A. F.

SOV/74-26-12-11/25
Sth Mendeleyov Congress. Section of Chemistry and Chemical Technology of Fuels
Plate, S. R. Sergiyenkol As D. Petrov, V. I. Isagulyants, G. N"
Maslyanskiyt V. A. Kobelev, N. R. Bursian, M. 1. Ryskin, A. S.
Fomina, L. Ya. Pobultp- Z. A. Degtyareva, A. A. Kruglikov, M. A#
blenkovskiy, A. N. Aleksandrova, K. Yu. Volkov, S. A. Gordon,
L. V. Petrovskaya, V. M. Ratynskiyj T. I. Sendullskaya, N. I.
Shuykin, T. I. Naryshkina, I. M. Artyukhovp D. I. Zullfugarly,
Bo A. Kazanskiy, S. I. Khromov, Ye. S. Balenkova, N. A. Seidovag
Al. A. Petrov, S. V. Adellson, T. Kh. Dlelik-Akhnazarov, I. I.
Mukhin, D. I. Orochko, N. A. Chepurov, V. N. Koz1ov are
mentioned.
Card 2/2

5(0) BOV/74-28-12-13/25
AUTHORS: Kozlov, V. V., Vollfkovich, S. 1.
TITLE: 8th Mendeleyev Congress, Section of Chemistry and Technology
of Silicates
PERIODICAL: Uspekhi khimiiq 1959P Vol 28, Nr 12p PP 1429-1431 (USSR)
ABSTRACTs The Section of Chemistry and Technology of Silicates (Refs 26,
57) was working under the guidance oft Academician AS UkrSSR
P. P. Budnikov;: Deputies: Academician of the Akademiya stroitell-
stva. i arkhitektury (Academy of Civil Engineering and Archi-
tectwe) N. A. Toropov, Corresponding Member AS Ukrainskaya. SSR
0. P. Mchedlov-Petrosyan; Scientific Secretarys Candidate of VZ
Technical Sciences I. V, Kravchenko. Secretaries were: A. Ye.
Rempell, N. V, Petrovykh, V. V. Myshlyayeva. Academician AS
Ukrainskays. SSR P. P. Budnikov, Academician of the Academy of
Civil Engineering and Architecture X* At Tor*opov, Professor
Yu. P1, Butt, Professor V. V, Stoltnikov, Professor 1. 1. Xitay-
gorodskiyp Professor I. F. Ponomarevq Docent S, M, Royak pre-
sided over the individual meetings. The following topics were
treated in the lectureBs General Silicate Chemistry; Chemistry
Card 1/2 and Technology of Ceramics and Refractories; Binders and Glaas,

P-
SOT/74-28-12-13/25
8th Mendeleyev Congress. Section of Chemistry and Technology of Silicates
Lectures held bys P. P. Budnikov, Yu. M. Butts S. K. Dubrovoq
I. I. Kitaygorodskiy, Yu. A. Shmidt, V. A. loffe, M. K. Call-
perin, V. 1. Minenko, 3. M. Petrova, P. P. Biidnikov, V. G.
Savellyev, 0. M. Astreyeval V. I. Guseva, N. S. Popov, N. S.
Zavgorodniyj K* 3, Kutateladzet W. G. Dzhincharadze, I. V.
Kravchenko, Ye. V. Podushko, L. N. Rashkevich, Yu. M. Butt,
V. F. Fedoryakin are mentioned. It is noted in the resolution
that the most important tasks in the field of chemistry and
technology for the next years are the extension of research
work and the improvement of operational processes.
Card 2/2

5(0) BOV/74-28-12-14/25
AUTHORSt Kozlovp V. Vol Volifkovichl S. I.
TITLE: 8th Mendeleyev Congress. Section of Radiochamistry and Isotope
Chemistry -
PERIODICAL: Uspekhi khimii, 19591 Vol 28, Nr 12, PP 1431-1433 (USSR)
ABSTRACTs The Section of Radiochemistry and Isotope Chemistry (Ref 27)
was working under the guidance of Academician A. P. Vinogradov;
Deputy: Academician AS Ukrainakaya SSR A& Is Brodskiy; Scien-
tific Secretariess Candidate of Chemical Sciences A. N. Yer-
makovq Candidate of Chemical Sciences 0. A. Nekrasova. Acade-
mician As P* Vinogradovt Corresponding Member AS USSR I. Yee
Starik, Academician V. I. Spitayn, Academician S. S. Xedvedev,
Academician AS Ukrainskaya SSR A. I. Brodskiyq Corresponding
Member AS USSR No Me Zhavoronkov presided over the meetings of
the Section. Lectures held byt A. P. Vinogradov, A. K. Lav-
rukhinat So So Rodinp A. A. Pozdnyakovs Is Pe Alimarin, Yu. A.
Zolotov, Yu. P. Novikovp P, No Paley# Ye. So Pallshin, G. N.
Yakovlev# I. P. Semenov, 0. N. Plerov, A. Do Gellman, Yu. Be
Gorlitq V, Me Vdovenko, Me Ps Kovallskayat To V. Kovaleva, A. A.
Card 1/3 Lipovskiy, M. 0. Kuzinaj L. No Lazarev, So Yu. Yelovich, B. X*

SOY/74-28-12-14/25
8th Mendeleyev Congress. Section of Radiochemistry and Isotope Chemistry
Preobrazhenskiy, A. V. Kalyamin, 0. Me Lilovat 1. Ye. Starik,
V. 1. Grebonshchikovap Re V, Bryzgalova, F. Be Chernyavskaya,
V. I. Bobrova, K. Be ZaboTenko, I. V. Kolosov, Ve V. Fomin,
An. No Neameyanov, Yee A, Borisovp I, Zvarap Be G* Dzantiyev,
B. A. Kuznetsov, A. D. Maliyevskiy, Ts. 1. Zallkind, No Be
Miller, 0. 8, Tyurikov, Go Z. Gochaliyev, V. 1* Veselovskiyj
N. A. Bakhq L, 0. Bugayenkoj V. 1. Hedvedovskiy, A* A. Revina,
L. So Polakq A. V. Topchiyev, No Ya. Chernyakq So Ya. Pshe-
zhetskiyj Me A. ProskuTnin, Ye. A. Shilov, F. Me Vaynshtayn,
L. L. Strizhakf As 1. Brodskiy, K. I. Sakodynekiy, So I.2obkovs
No Me Zhavoronkovt A* A, Balandinp, V. I. Spitsyn# L. 1. Bar-
kovap V. I. Duzhenkovj Yuo S. Lazurkin, Me A. Makullskiy, No 11,
Sevryugova# 0. V. TJvarovp So I. Babkov, G. No Chernykh, V. A.
Sokol'skiy# No Me Zhavoronkovt I. Be Rabinovioh, We He Tuni-
takiy, M. V. Gurlyev, Me V. Tikhomirov, V. L. Talfroze, Ye. L.
Frankevich are mentioned. Out-of-program lectures were hold byz
I, P. Selinovj No No Krot, A. G.-Kozlov, V. Ps, Shvedov, A. V.
Stepanovp Me Me Senyavinp I. Ya. Petrov, Vo L6 Karpovp Ve A*
Nikishina, V. P. Meshoheryakov, B. So Kirlyanov, A. P. Smirnov-
Averin, B. V. Ershler# M. A. Nezhevenko, Go G* Misishcheva,
Card 2/3 1. V. Vereshohinakiy, A. K. Pikayev, P. Ya. Glazunoyt Ya, No

BOV/74-28-12-14/25
8th Mendeleyev Cong3~eos. Section of Radiochemistry and Isotope Chemistry
Varsh;-.vskiy, V. L. Karpovp I. Ya. Petrov# Z. S. Bulanovskaysp
A. M. Hozen, A. B* Anufriyev# A. D. Bondarl, N. G. Zaytsevaq,
Lo Weng-chung.
Card 3/3

5(0) SCV/74-28-12-15/25
AIJTI--'ORS: Kozlov, V. V., Voltfkovich, S. I.
TITLE: 8th Kendeleyev Congress. Section of Theoretical and Applied
Electroclieuistry
PERIODICAL: Uspekhi khimii, 1959, Vol 28, Kr 12, PP 1433-1436 (USSR)
ABSTRACT: The Section of Theoretical and Applied Electrochemistry (Ref 28)
was working under the guidance oft Academician A, No Frumkin;
Deputy: Professor So I. Sklyarenko; Scientific Secretary:
Candidate of Chemical Sciences To V. Kalish. Academician
A. N. Frunkin, Professor Ya. M. Kolotyrkin, Corresponding Mem-
ber AS USSR and President of the Akademiya nauk Litovskoy SSR
(Academy of Sciences of the Lithuanian SSR) Yu. Yu. Matulis,
V. I. Veselovskiy, Academician AS Ukrainskaya SSR Yu. K. De-
limarskiy, Professor Ya. V. Durbin, Doctor of Technical Sciences
L. N. Yakimenko, Professor N. Do Tomashov, Professor B. No
Kabanov, Professor Yu. V. Baymakov presided over the individual
meetings of the Section. Lectures held by: A. N. Frumkin, L. M.
Yakimenko, Yu. V. Baymakov, S. I. Sklyarenko, V. V. Stender,
R. I. Agladze, A. I. Ni:~hnik, N. A. Izmaylov, 11. P. Nikollskily,
M. M. Shul'to, N. V. Poshekhonova, A. 1. Parfenova, 0. V. Ma-
Card 1/2 zurin, N. Ye. Khomutovp I. So Golinker, V. G. Levich, Ya. M.
L'-1

SOV/74-28-12-15/25
8th Mendeloyev Congress* Section of Theoretical and Applied Electrochemistry
Kolotyrkin, L. A. Medvedeva, N. V. Nikolayeva-Fedorovicli, 0. A.
Petriyt A, N. Frumking, S, V. Gorbachev, M. A. Loshkarev, 1. P.
Chernobayev, B. I. Tomilovq A. G. Stromberg, D. P. Zosimovich,
B. N. Kabanov, A. T. Vagramyan, A. P. Popkov, N. T. Kudryav-
tsev, G. K. Smolenekayal V9 M.-Karataveval Ro G. Golovchana-
kaya, V. V. Andreyevp T. P. Stapanovap Ye. S. Volkova, I. V.
Krotov, V. M, Berenblit, I. Ya. Lantratova, A. I. Shultin,
G. I. Volkov, D. P. Semchenko, K. G. Illin, M. F. Lantratov,
A. Ya. Alabyshev, Yu. Yu, Matulis, K. M. Gorbunova, %. M.
Polukarov, 0. S. Popova, A. A. Sutyagin, G. M. Kamarlyan,
I. L. Rozenfelld, V. P. Maksimchukv L. K. Lepin', A, Ya.
Vayvade, A. K. Lokenbackh, Yu. K. Dblimarskiy, K. H. Kalabina,
V. V. Kuzlmovich, T. P. Kaptsova, S. I. Sklyarenko, V. I.
Konstantinov, Ye. A. Markina, V. M. Amosov are mentioned. In
the resolution, it is stressed that a broad-scale introduction
of electrochemical production methods into industry is re-
quired, if the tasks of the 7 Years Plan are to be fulfilled
Card 2/2

5(0) SOV/74-26-12-16/2.5
AUTHORS: Kozlov, V-. V*., Vollfkov--i,.h, Be 1~,
TITLE: 8th Hendeleyev Congress. Section of the Chemistry of Metals
E,.nd Al-lo-y-s-
PERIODICAL: Uspekhi khimii, 1959, Vol 28, Nr 12, PP 1436-1437 (USSR)
ABSTRACTt The Section of Chemistry of Metals and Alloys (Ref 29) was
working under the guidance of Corresponding Member AS USSR
N. V. Ageyev; Deputy: Profsssor I. I.Kornilov; Scientific
Secretary: Candidate of Te.,hnical Sciences R. S. Polyakova.
Academician I. P. Bardin, Irofessor Ye. Ye. Cherkashin,
Professor Ye. M. Savitakiy, Professor Ye. S. Makarov, Professor
I. I. Kornilov, Correspond-.ng Member AS TISSR N. V. Ageyev
presided over the individual meetings of the Section. Lectures
held by: N. V. Ageyev, I. I. Kornilov, Ye. 11. Savitbkiy, A. 11.
Yevseyev, Ya. I. Gerasimov, A. V. Nikollskaya, A. Yp-. Shonyayev,
K. G. Khomyakovt V. A. Troshkina, Yu. D. Tretlyakov, Ye. Ye.
Cheburkova$ T. A. Borcheva, M. F. Alekseyenko, Ye. L. Bush-
nanova, L. V. Zaslavskayat S. T.-Kishkin, G. F. Orekhov, A.
F. Platonoy, N. Me Popova, G. Me Rovenskiyj K, P. Sorokinap
Card 1/2 11. 1. Blok, K. F. Lashko, I.I. He Kozlova, Ye. S. Makarov, Ye. I
LX

SOV/74-28-12-16/25
6th Mendeleyev Congress. Section of the Chemistry of Metals and Alloys
Gladyshevskiyp P. 1. Kripyakevichp Yu. Be Kuzlmap Yu, No An-
dreyev, G. So Zhdanov, V. K. Grigorovich are mentioned. A
joint meeting together with the Section of Inorganic Chemistry
and the Section of Physical Chemistry was held on March 18.
Lecturers weres No No Sirotaq Be F~* Ormont, Lo Go Dudkinq Z. Go
Pinakert Yao As Ugay# No A. Goryunova,.In the resolution, the
necessity to extend considerably work in the field of physico-
chemical an lysis, the study of phase diagrams, and the crystal
chemistry of metal alloys was stressed.
Card 2/2

5(0)
AUTHORS: Kozlov, V. V., Vollfkovich, S. I.
TITLE: Sth Mendeleyev Congress. Section of Colloid Chemistry
PERIODICAL: Uspekhi khimiit 1959, Vol 2a, Nr 12p PP 1419-1422 (USSR)
ABSTRACT: The Section of Colloid Chemistry (Ref 19) was working under
the guidance of: Academician P. A. Rebinder; Deputy: Doctor of
Technical Sciences N. V. Mikhaylov; Scientific Secretary:
Professor G. 1. Fuks. Acz,.demician P. A. RebinCer, Academician
AS Belorujakaya SOR N. F. Yermolenko, Professor Ye. N. Aleksand-
rova, Corresponding Member AS USSR B. V. Derya~;in, ProfesGor
M. Ye. Shishniashvili Dreoided over the individual meetings of
the Section. Lectures held by: V. P. Smilga, B. V. Deryagint
N. A. Krotova, L. P. I-lorozova, Yu. P DeyneGa, A. V. Dum,--nskiy,
G. V. VinoGradov, I. Ye. Neymark, V. V. Karasev, B. V. DeryaGiii,
G. I. Fuka, M. S. Ostrikov, S. I. Popell, N. V. Pertsov, N. F.
Yermolenko, Z. A. Krivchik, A. B. Taubman, S. A. Nikitina,
P. I. Yermilov, I. Yo. Neymark, P. V. Moryganov, B. N. 1-11clInikov,
V. F. Androsov, A. A. Kharkharov, V. F. Boyko, Ye. D1. Aleksand-
rova, V. N. Tsvetkov, N. S. Razumikhina, A. 1. Yurzhenko, R. V.
~
Card 1/2 Kucher, A. B. Taubman, A. F. Koretakiy, M. A. Kovbuz, S.N. ~

8th Mendeloyev Congress. Section of Colloid Chemistry SOV/74-28-12-7/25
Levi# Z. Ya. Berestneva, V. A* Karginp B. V. Deryagin, Yu. M.
Glazman, D. N. Strazheskop E. M. Natanson, S. Ye. Kharin,
K. 8. Lyalikovq P. M. Silin, P. A. Rebinder, Ye. Ye. Segalova,
M. P. Volarovich, I. V. Churayev, N. V. Mikhaylov, Ye. Ye.
Kalmykova, 0. Pe Mchedlov-Petrosyan, F A. Latyshev, A. G.
Dunakov, H. A. Lovchuk, V. I. Yakimova: S. L. Talmud, K. P.
Mishchanko, As A. Morozov, S. N. Stavrov, L. I# Belen'kiyj
1-1. Ye. Kazanskaya, T. V. Bromberg, P. A. Demchenko are mentioned.
In the resolution taken by the Section, it was pointed to'great
progress achieved in applied theoretical colloid chemistry in
the USSR. The attention of the OKhN AS USSR was called to the
advantages of establishing an Institut fiziko-khimicheskoy
mekhaniki (Institute of Physico-chemical Mecbanics).
Card 2/2

5(0) SOV/74-28-12-17/25
AUTHORS: Kozlov..V. V., Vollfkovich, S. I.-
TITLE: 8th Mendeleyev Congress*~Section of Ecbnomical Planning, and
Organization of Chemical Plants
PERIODICALt Uspekhi khimii, 1959P Vol 289 Nr 12, PP 1437-1439 (USSR)
ABSTRACTs The Section of Economics, Planning, and Organization of Chemical
Plants (Refs 30959) was working under the guidance of: Cor-
responding Member AS USSR N. N. Nekrasov; Deputy: Professor
No Pe Fedorenko; Scientific Secretary; A. Lo Rabkinao Cor-
responding Member AS USSR K. No Nekrasov, Professor So A. Per-
vushin, Professor No P. Fedorenko# Professor L. Is Raytburg,
Professor As Is Dzens-Litovskiy presided over the individual
meetings of the Section, Lectures hold by: No No Nekrasovt Po As
Khokhryakovp Go F. Borieovich, A. I. Ravdel', No A. Zeligman,
V. Go Fridenberg, So A. Pervushin, So Yes Rachkovskiy, N. P.
Fedorenko, Yes P. Shchukin, N. P. Fedorenko, G. F. Borisovich,
P. A. Borisq, ' . A. L. Rabkiha, Is V. Rostanin, Go Ye. Birger,
Yes P, Ivanova are mentioned. In its resolution# the Section
has pointed to the fact that the fulfillment of the 7 Years Plan
Card 1/2 requires a detailed study of methods to be used for the most

SOV/74-28-12-17/25
Sth Mendeleyev Congress*- Section of Economics# Planning, and Organization of
Chemical Plants
effective utilization of material and manpower resources. The
attention of the Gosplan SSSR (State Planning Board of the
USSR), Otdeleiiiye ekonomicheskikh nauk AN SSSR (Department of
Economical Sciences of the AS USSR), Goskomitet Soveta Ministrov
SSSR (State Committee of the Council of Ministers of the USSR)~
and Ministerstvo vysshego obrazovaniya SSSR (Ministry of
Higher Education of the USSR) was called to the necessity to
improve and to extend the treatment of economical problems in
chemical industry. Moreover, the tasks of the Institutes of the
Academy of Sciences and of the State Planning Office of the
USSR were discussed. It was pointed to the necessity to promote
training in economics at chemical colleges, and to increase the
publication of specialized literature treating questions of
economics and planning of chemical production.
Cara 2/2

5 (3)
AUTHOR: Kozlov, V. V. SOV/79-29-4-65/77
TITLE: Investigations in the Anthraquinone Series (Issledovaniya v
ryadu antrakhinona),XXVII ' On the Hydrolysis of the 1,5- and
1,8-11itrosulfo Acids of Anthraquinone (1,.5~- and 1,8-ilitroxyan-
thraquinone)(XXVII.0 gidrolize 1,5-i 1,8-nitrosullfokislot
antrakhinona 0,5-1 1,8-nitrooksiantrakhinony)).
PERIODICAL: Zhurnal obshchey khimii, 1959, Vol 29, Nr 4, pp 1344 - 1349
(USSR)
ABSTRACT: The authors continued their previous investiCations of
hydrolysis in the series of anthraquinone (Refs 1-4) and invest-
igated in the present paper the influence exercised by the ni-
tro group upon the hydrolysis of the sulfo group in anthra-
quinone, proceeding from the anthraquinone-nitrosulfo acids.
Except a patent (Ref 5) nothing has hitherto been published on
the hydrolysis of these compounds. This patent describes the
hydrolysis of the 1-nitro-8-sulfo acid of anthraquinone in
sulfuric acid of 5VIa with mercury at 1'90 _ 2000, under forma-
tion of the a-nitroanthraquinone. It was found that the hydro-
lysis of the 1,5- and 1,8-nitrosulfo acids of anthraquinone in
Card 1/3 sulfuric acid and water without participation of mercury salts

Investigations in the Antairaquinone Series . . S07/79-29-4-65/77
XXVII..On the Hydrolysis of the 1,5- and I,B-Nitrosulfo
Acids of Anthraquinone (1,5- and 1,8-Nitroxyanthraquinone)
is possible in the open as well as in the closed system at
high temperature. The hydrolysis in water, in fused tubes,
leads to the formation of the hitherto unknown 1,5- and 1,8-
-nitrosulfo acids of anthraquinone by the substitution of the
sulfo group by hydroxyl in the initial product. The hydrolysis
in concentrated sulfuric acid proceeds in the open system under
formation of the a-nitroanthraquinone by the substitution of the
sulfo group of the initial product by hydrogen. The hydrolysis
with sulfuric acid in fused tubes proceeds under.formation of a
mixture of products which are produced by the substitution of
the sulfo- as well as of the nitro group of the initial product
by hydrogen and hydroxyl. The hydrolysis with concentrated sul-
furic acid is in these two systems complicated by the oxidation
processes. The presence of the anthraquinone-l-sulfo acid in
the Position 5, and especially in the position 8, inhibits con-
siderably the -lobility of the sulfo group, compared with the
behaviour of the sulfo group in the 1-su,lfo acid or the 1,5-
and 1,8-disulfo acid of anthraquinone. The tables show the hy-
Card 2/3 drolysis results under various reaction conditions (time, system,

1.
Tnvestigations in the Anthraquinone Series. SOV/79-29-4-65/77
XXVII) On the Hydrolysis of the 1,5- and I,B-Nitrosulfo
Acids of Anthraquinone (1,5- and 1,8-llitroxyanthraquinone)
temperature, water volume, acid concentration. There are 5
tables and 8 Soviet references.
ASSOCIATION: Moskovakiy institut narodnogo khozyaystva imeni G. V. Plekhanova
(Moscorv "Institute of National -Economy*. imeni G. V. Plekhanov)
SU-13LTITTED: February 8, 1958
Card 3/3

BROZOVSKtY, D.I.; KOZLOV, V.V.
w.
Using tr'i'"-oxynophthalenes as oxidation dyes for furs. Kozh.-
obuv.prom. 2, no.6:18-20 Je 160. (MIRA 13:9)
(36es and dyeing--yur) (Naphtlkilenetriol)

LEEEDEVj N.N.; BALTADZRIj I.L; KOZLOVp V.
Effect of the activity of catalysts on the relative reactivity
of toluene and benzene during chlorination. Zhur. VKHO 5
no* 2:236-237 160. (MM 14:2)
lo Moskovakiy kbimiko-tekhnologicheakiy institut imeni
D.I. Mendeleyeva.
(Toluene) (Benzene) (Chlorination)

KOZIOV, V.V.; BROZOVSKIY, D.I.; GAVRILOVA. V.M.
Naphthalene Beries. Part 19: 1,3,7- TriVcIroxy-naphthalene. Zhtw.
ob.khim. 30 no.8:2714-2718 Ag 160. (MIRA 13:8)
(Naphthalene)

,z_KOZLOV, Y.Y.; SILAYEVA, YO.A.
Anthraquinone series. Part 31: Sulfonic acids of trans-
dibenzopyrenequinone. Zhur. ob. khim. 30 no.11!3766-3772
N160. (HIRA 13;11)
1. Moskovskiy institut narodnogo khozyaystva Imeni G.Y.Plekhanova.
(Dibezizopyrenequinone)

Q KOZLOV, V.V.; VICSFWVSKATA, I.K.
Naphthalene aeries# Part 20: Kinetics of the reaction of ot-naphthol
with aqueous solutions of ammonia and a=onium oulfite. Zhur. ob. khim.
30 no.12.-4088-4092 D 160. (MIRA 13:12) ~
14 Moskovkskiv Institut narodnogo kho2yaystva imeni G.V.Plekhanova.
. (Naphthol) (Ammonia) (Ammonium sulfite)

KHRUSTALEVA, V-N.; KOZLOV, V.V.
Colorimetric determination of inulin, Izv. vys. ucheb. zav.;
pishch. tekh. no.4:152-156 161. (MIM 14:8)
1. Moskovskiy institut narodnogo khozyaystva imeni G.V.Plekbanova,
laboratoriya, organicheskoy khimii.
(Inulln) (Colorimetry)