SCIENTIFIC ABSTRACT I.L. DEREVINSKIY - K.M. DEREVLEV

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• Collection: Scientific Abstracts
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• Document Creation Date: January 3, 2017
• Document Release Date: July 27, 2000
• Sequence Number: 6
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

DVR VINSKIT,1,1L.
Vlaximm stresses produced in idre ropes by winding In the process
of their manufacture. -lauch. trud7 XNlUl no.2gl22-129 158.
(MIRA 1338)
(Wire rope) (Strains and straBses)

BEL1,1100Y, D.I,.'., k--nd.tokbn.naul,-; R-~&M:116--KIY, I.L., innh.; L.M.,
luzh.; 'GO-RX, R.A.,
Invas'ui~.-,.ttiac~ round-lin.,c chiins tor mino conv-~Yt?rs. Nalich.tIoU.
vxls.sllkol.~; -or.dolo no-:~:1)13-147 '59. ( 1.11 R.A 12: 7
1. Predstavlaria kafedroy ro.-w-r1cli i ru~nichnj.,.o trms-3orts
:zy)

BELENIKIY, D.M., dotsent; DEREVINSKIY, I.L., kand.tekhn.nauk
Study of the parameters of the bearing oprings 4 belt and spring
conveyor. Izv. vys. ucheb. zav.; gor. :;hur. 5 no.10:105-110 162.
(MRA 15:11)
1. Karagandinskiy politekhnicheskiy inatitut. Rekomendovana
kafe&oy prikladnoy uekhaniki.
(Conveying machinery)

DEREVINSKIY, I.L.0 44,nzh.
~
Determ_;aing the IiftW span of a ballasting machir.e. lzv.-%Ts.ucheb,,
zav,j ma3hinostr, no.,0134-137 164. (MIRA 18%1)
1, Kax-agandinakiy po2-itekhnicheakiy institut.

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Rellstioax between the dillfusion rate and equallaing power
of subabod forvinowilbor.
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Ohl'tugh lux-ous plair (%,Rlko, C. if. J9, 31141) it., 11.11
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ilk. The diffuslon I'MIC ilk in%'rl-Wly 11114"liMIAl lit I It,'
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DIMITSUTA, V.I.; KOZLOVA, Tu.S.; ROGOV3, Z.A.
----,nl,-es-tig^,-a-t,iug the comparative reactivity of thei hydroxyl groups of
cellulose. Soob.o naueh.rab.chl.VIHO no-3:9-12! '55. (MIRA 10:10)
(Hydroxyl group) (Celluloset)

An
~i Of taUidottai
VI.
'
dk&U,30 ma hun. Der -Aya, jjl

:b1tri-I
tim
Omn
Jt~ of oenulne byd=yl zn?m 441ijbution oil =eft"V
ar-
mnta l1wing Partial laeftlation ofttunllsq jwpa~cal~, alkiUw"~
Yu. KoAos-j~ "d Z. h.
-97 1U
t-lanlifwW after trtlaaent iu Nand 1"ITt"'. mmh'~'j hmwithj L.:
vilphalo. Ile p ~'w~est C3.1;1 ivity
d~-.pizjpO by hjdmxy. grmi~p5, thio rom- t-F::r (&-m. i
'MA
an., Oxidr%tiv
c
~jE:~p'wcA that rlistfit~uii~ll of nA utaform.
with 1=78-5 (y~-siamlxr ai s~31),titntA group!
ghi~D-lt units) IDwed 20 motboxyl g.-pup dhWbIlmd
-cop.
and S. 5 on C'r, , Vor this -10, 01i"tht: sm, dirty C atvi is, tht~ no,
t;rollps per 100 ghacos-2 JriWic.-Js -wmild be ex-mkic-d to be.,
A
'01`4.xtion to~' it
rn~thylululr,5t! with --1:02. Om n-n.1of frce rlycul gruuj~- P4:1.11w:
Vid afta. nethyh L lon ;.t wot
"rl--)n atrims it wa-q, j 1. M;Iributicu oi niexh,~:tyl in alka
;V5WrW
s'lliflosp Iva!) LISO identkal and Oluw,'-J~ -e nearto 1buillilLtlitt"t ;k,
oid nott~

)WKCYANOV, I.B.;1NMANTS, 1.14;SR)WAKIN, M.M.;,30GOSWVSXIY, B.M.;
SKMATOV, S.X.; K(RflMi, A.A.; NCMI'TSXALk. V.A. ; ROGOVIN, Z.
In memory of A.A. Strepikhesv; obitywry. Ithur.ob.khin.26 no-11:3224-
3226 N 156, ()WA 10:1)
(Strepikheov, Alelmwndr Alskennilravich, 1912-1953)

u pro.
3.
Af,'N M,
and 2. Rogo,in 1,,rztw1cTta'r,7,
Kkim, 26
-'Meth";~IuZtprrpa. ji5ioda kna mo
00.una
110-&-Iiu~le rulniceof-r-u NQI~ (th or from tzethylA--
'P ~(Pbcu))N
prm=ce of~l the J~Mlrj~~ 110i
(n) of,caala!t U-C taort r4utilre S~(ttAt approx,
as ManY MtO
geolqs art forme4l on thrit grollps P.3 on
ibe primary opo. by~
wed.
by wringing, a0pirusivii iz'tobuzq!hnJ tv~atmfnt with.
a5TO '44aOlli 4 llr3. at 04. do =rthy40on. with Mel~
bm'st 40* and'26 brs. at ~V), or with Idt'2M (37~ hrA- i
1%35 und %'F to 33 11M 1~t 2DI), cts rallre stlectivfly'
~'rj ck'w
.~o that Blinost n the rea
4t;f 1 the methybtion with -MesSO results in neigly eqF71wd
b . I
I
'm Ut)op vf'-NIO) grbups b~tvreen C~ alld C pii5ition
Mel tr~abrelll ho"'ever, there Is t6idency for the McOi
IVOUPS to he ~;ateAprimaxiiy at ent of the~stcondary C
titoms. The MbItsiia-11cate that the vwuom ni at HO
J1 J.'roups wlik" hals tbi-, oppon-tunity to vtact witr&.e base In
the suspr-nding tue(jium. LVIE. Ccinpmratloe reettivity
hydioxyl groaps of ttljulwt. 3. DistrIblytion 0" Meth-4;
CxYI grcip in prtislly metIqlated v~llulvse tobtaLi-A b
of
rlethylatiw ou With diaromOlmna. Jba. IlS74-6..
-~-Tvatnirrt of I, g. dr), v6cu:ia Silk Willi NO rrj. 1:1-0 uiln
of 0.511,1 CII.N,i cozag, 2.61sr!l. 11.0 at 2* kr iip to,
'F

gave 1.
analyzed by tritylathin aW oxiilation with Ilt0j, &WIved
that the 11 are mo3t rt=,ive vv~.jth CI.J2.1;j. TI)e no. 4.1 W
,YhVh urt thus stitthylattil is2 %imcs follmllon plWary
HO gmup. AS the rrsult of Oxillation of Irre Fly4Aie
groulls it "U'.1 C'hmn that, V103WA) gn'llpq tentl W bv iiKplt~d
pflinalily at will of tht. ;M,~~'
jk4

A -
DE;iMVITSXAYA, V.; KOZLOVA, Tu.; ROGOVIN, Z.
w9ft
Relative reactivity of cellulose hy(iroxyl groups. Part 3. Distri-
bution of aethozy groups In partially methylRted cellulose obtained
by cellulose mothylmtion by dimsomethane. Zhur.ob.khim. 26
no.12:3374-3376 D 156. (MLRA 10:7)
1. Mookovakiy tekstillnyy inqtitut.
(Cellulose) (Metbylatlon.)

%! . J*i. I , Y.!NA, !.l. , !, Al i~(,)OOVII;, ;~. i,.
-4.~
"Reactivity of the 011-ct;roups of cellulf)sc- durinbr wthylotion.", D
i,amr -,,-)resen'ued at the ~-,Ii Cor~;ress on, the Chonnist'ry and P'n.,A-cs of -jgl~
- 4
23 Jan-2 re' 5'i , "Osc-M-1, "ext-11C Rc!sca,'c'h. Ins": -
- V; I U.
B-3,OC4,395

JENNE
)T
IT, 11ps
lang
in -A' 11-Sbi'llimt jjv i f motiv) ith:t~
LXVIC Prpprr~li~s,Qf
ga
wV-1fion frvm N-A. Alf C,
is k~I-Idkij ~,I
b w-e zz lb~ ifitmiqdiale znv; ;x_
czt: COSI, ~di C,
mn
ovl,~r cd m;i6litl~ i!1 21A, 11-ol
h--3 101iows.

LUTHORSt 1) e r e v -J 1, s kay,-- V,. P r o k ~ fa M, ~Cj-28 ;z. ~7/6-i
TITLE-. Inves,.-igation of the Ccmparat,lve R~artvy--.,Tv of th-~
Hydroxyl. Gi-oupe of Cellc-];~se ( 'js~-Iedovaniye sra-irnitellnoy
reaktai-onn.,)y sposobnosti gid~oksillnykh grupp tsa1.1.yvlozy)-
V. On the Distribu-c.lci-,, of +)-o-, Mle'licky GLouus "n the Par=
tially Methylatled Cellulose Which. was Ob-,,~ained ir. an A2ka=
lin-r Me~.ium 'Nith Different Concentrarion,3 of Alkali Liquor
(V~ 0 raspredelenii inetoksillp,ykh 17rupp v chastichno metili-
rovannoy tsellyuloze.. poluchenrioy shchelochnoy srede pri
razlichnoy kontsentrataii shchi:lochi)
PERIODICALt Zhurnal Obstvhay KhAMii. 1958. Vol. 28,, NT 3,
PP. 7h6--7!8 (USSR)
ABSTRACT: In an earlier work by the authors (Ref, 1) they reported
on the resulta of the irv-esti&&~ion of the reaotivity of
th-e- hydroxyl. groups in cellulose on the action of an ~8%
alkali liquor., as wall aq on the subsequent methylation.
In the present work the react ion .v-,th S., I", and 44 liquor
was caryied outs The alkaline -eilulose wa!~ sqveezed to one
Card 1/3 third of its weight in order to l-ibera,.e 1~ from adsorbed

Investigation of the Comparative Reacta.vity of tha
Hydroxyl Groups of Cellulose. V.. On th,! Di-qtribuTion
of the Methoxy Groups in the PaTtiallY Methylated Cellulose.
Which was Obtained in nn Alkaline- Meda-um With Diffezent Ci~n-
centrations oC All-ali Liquor
alkall. ther, it was wasl,,,J with dry isobutylal,:~Chol and
finally it was MCfIlylatE-L. In some ~,aqos algo the squee.
zed., bu-~-. n.:A yet washfA alkalic,-.~llulose was methylated.
The fcour -qtIF-,q gJvc- inforipatiori oil the P;,-ef hy lilt I oil rc-
sults of alkalized they rpad,~ '"Sha d.Latr;1b,.ztiCr1
of the methoxy groups wa5 .n-,rest:~gat--~d in the- partially
methylat,~d oellulre-~ which had bee- by the actio,".
of methyl an the al'.%lized cellulos,~ w~-,,h coriceLtra--
tion of the liquo:r taken for "be production of alkali cellu-
lose (--rom 6-44',. The f,.r:na',Aojr. of thE- rear-tion of alkaii
j.
oellulo-se and th4
p 1~ a._ j~t, t1te
expense of the secondary hydroxyl groups m,~,~,T. iTarj,,.1djy with
a liquor concentration o-~. Jol,'oo. D'. thr- of the
not washed alkal J. cf-11113o'c-, obta3ilea by th;~ a~-tlQll of a
4o% alkali solution the au,.hc-rs obtainel a methyl collulose,
wi4l.h a considera-bly great.!77 conten-- of a!k-aii c,-~Iluiose
than is the case wi.i.h meth~rl GellulDse resulting t'r,)m th(!
methyla~j.on af a aashed P-11raij, cellulos-; this 44v
Card 2/.3 ii:qely axplrtiri~-d by srj of tbe F~-Jkali=

Investigation of the Comparative Reactivity of' the 79-28-3-35/61
Hydroxyl Groups of Cellulose. V. On the Distribution
of the Methoxy Groups in the Parti-ally Methylated Cellulose
Which was Obtained in an Alkaline Medium With Different Con-
centrations of Alkali Liquor
cellulose. (Isobutylalcohol being used in the washing
of the adsorbed alkali!).
There are 4 tables and 2 references, 1 of which is Soviet.
ASSOCIATION: Moskcvskiy tekstilInyy institut (Moscow Textile Insti-
tute)
SUBMITTED: January, 17, 1957,
Card 3/3

AUTHORS Dprevinalaya V,. 28 - 6.1
TITLE- Investigatio.-j. of tbe C,~mpaxza7,-ve of th-~
llydTox-ylgi-oup~3 C~-.Iluiros? ln.~y
reakt-siorinoy spi,lq,0l,ii;)si--- gri-q!) ~selklyl:.Iozry)-
VI. On the Dist:.- ioti of th,~ M-rhyla-ri.~:n Prodii(.'..:- .)f the
Na.-Alcoholata c' Cellul-t~ (V-1. -.1 rcrpred~~Ierdi 'Metoksil-l-
nykh grupp -~r produkt?-.kh Na-alkegolyata
tsellyll-lozy)
PERIODICAL- Zhurnal Obsbobey Kb-mid. 12~1-, liv
pp., 118-7?1 (USSR)
ABSTRACT. AlThough -the forma~,',:)rj of th-~~ --?Ilulos-? in
liquid ummon-Uq. haq b-:3c--.n irive0,gaKei by Lany scientists
ther,- hae been ii-) 22ea.r da~F~ 7r, reac-:5,"',
y of the
bydT~,).-j! gTOUPEi 1~~ Th~ w;th
Ila so f-L-r Th.? aulhors taF-ic~ The svn-he~,is
of the uIc-'holave al-11 thiL Ine~,sill-ment tn~~ 'U~~c--Aty of
the fornalior. cX hvdr-~ger, va~ -d t
01 na 0
Card 1/ 4 Shoyyg-Ln Y%R---if ~ ?)c The ey
d

Investigation of tfie Coripai~al j 1: 1 Ro, - i : -1 , v . f *7 ~ - '-1 6/
Ilydroxylgroupu of Cr.,I VI,, On thi. DI s,-T
of the lalethylatior, Prcidu-,~-i of i,h~ Na. LI
Cellulose.
sulfitozC11lulm-~ and visc~,5~ rwv~n
foxma+j.,~-n of -,a-:h -hydTc-~n a, n, Iq the
Oil UIF~ wit!) .-,r fh~~ body
Was detixiii-L.-tied. Dupundl I,g -)EI th,- U- 'I.F~t rf-
dii.e.ed sodi.im thi2 velo-ily di,invd;th, b-:,fw,7--n tlie
du:-a~ion of the formari--~o of the s-ond ard '-h--Ird
J~-hydrojjpn atom ir, bow-cn,er pract j,--al ly
constan- (-~dbl.es 2.) The -ommarv ve?o-iry ard.
e dep-nd on th., ~It"Tas~e-, Of the
TI, ia+Jto T
PrIpaxaJi-on. Tr--~ .1f Ilt?ima"loik the
fiTSt hydrngen a-or) th~-At of th~ th-.T-i
6. .,8 f o i (i in th-? ac, Jon on viscose rayon-,
in the :,a,,,o of the g.-rcunl -1 ~ .8 f 0:1 -j/t 1) e
dif f erer f, eimmaTy Tea. - ~~ on vell .::'. I T.Y a 1:8-1 , . The
authors ass,;xt~ th~ ut-a~ in 'lie ve3oCI-.-Le,5
of formai.-*~O-n of the 17~ all hy'L7:i-,ger, alom~3 ir. This rea:~+,4;,n
must be explained by, th- differ--2r," rE-3-t-i )-l"Y of the hydTo-
xylgroups of f,' '.r d,, 1- 14 out 1 on
Card 2/ 4 rf sciv,~m it) th~ -41oliii-~,-I-ry* li-mbpy- ot,

Investigation of the Comparative Reaotivity of the 79-28-3-36/6
Hydroxylgroups of Cellulose,, VI. On the DiatT-ibutien
of the Methylation Produots of the Na-Alcoholate of
Cellulose
of cellulose had to be determ-ired. Therefore a methylation
of the alcoholates was carried out at r = loo.-2oo (kr= con-
tent of alcoholate in relation to sod2UM) and the distribu.
tion of the methoxylgroups in the synthetized methylcella-
loses was determined. Before this the ammonia was completely
removed by blowing with dry nitrogen. The methylation took
place with methyl iodide in the course of 12 hours a methyl
cellulose with a very small content of methojqrlgroups (I ,U -
2%) having been obtained. By repeating the sodiumammonia
treatment and the methylation -this content was increased.
The results of methylationshow (table 3) that the formal
tion of the alcoholate and the methylation take place ex-
clusively at the expense of the secondary hydroxyl group-);
L.Iva further reaction of the foxiftation of the alcoholate a,,
&oo and its methylaiion takes place at the expense of the
primary hydroxyl group of the cellulose.
Card 3/4 There are 5 tables and 5 references,, 2 of which are Soviet.

Investigation of the ComparaLive Reactiirity of the 79-28 3--36/6,
Hydroxylgroups of Cellulose. VI. On the Distribution
of the Methylation Produots of the Na.-Alcoho)ate of
Cellulose.
ASSOCIATION: Moskovski.y tekstillnyy institut (Moac,~w Textile Institur-)
SUBMITTED: January 17., 1957.
Card 4/4

AUTHORS: Derevitska as V.. Prokoflyeva, if., 79-28-5-58/69

TITLEs Investigation of the Comparatiye Reactivity of
the Hydroxyl Groups of Cbllulose (Issledovaniye
sravnitellnoy reaktaionnoy sposobno5ti gidrokailln.,rkh
grupp teelly-alozy)
Me On the Distribution of the Methoxyl Groups in the
Partially Methylated Cellulose obta4.ned from Cellulose
Treated With Sodiumisoamyliate (VII. 0 raspredelenii
metokeillayldi grupp, v ehasticbno metilirovannoy
tsellyuloze, poluchennoy iz tsallyulozy, obrabotanmoy
izoamilatom natriya)
PERIODICAL: Zhurnal Obshohey Khimii, 1958, Vold 28, Nr 5,
ppo, 1368-1371 (USSR)
ABSTRACT: Starting from,the condition that in cellulose only one
hydroxyl M411with increased acidous properties exists,
the formation of an alcoholate can be expected not only
by the direct action of metallic sodium but also by means
Card 1/3 of a conversion with an alcoholate of ordinary alcohol.

Investigation of the Comparative Reactivity of the 79-28-5-58169
B~ydroxyl Groups of Cellulose.
VII. on the Distribution of the Methoxyl Groups in the
Partially Methylated Cellulose obtained from Cellulose
Treated With Sodiumiaoamylate
The experiments by Rassow and Wadewitz (reference 1)
to obtain a sodium alcoholate of cellulose this way
were not successful probably because they carried out
the reaction at a great excess of alcohol which had
to lead to an: alooholy81S of the formed cellulose
alcoholate. imorder to avoid this it was necessary
to use a sodium alcohqlate 4issolved in!inert solvents.
In the present papor a sodium derivative of cellulose
was obtained by the action.of sodiumisoamylate on
cellulose in tin inert solvent. Cotton cellulose served
as initial substance, which had earlier beemreated with
alkali and finally had been included (reference 3). Iii
this conversion only that cellulose treated the alakaline
way proved to be reactive. rhe alcoholate of cellulose
experimentally produced in -two different ways was then
methylated with.methyliodids. In order to determine the
Card 2/3 distribution of thet methoxyl groups in methyleelluloses

Investigation of the Comparative Reactivity of the 79-28-5-58/69
Hydroxyl Groups of Cellulose.
V11. On the Distribution of the Nethoxyl. Groups in the
Partially ikethylated Cellulose obtained from Cellulose
and Treated With Sodiumisoamylate
the number of free primary hyd.roxyl groups was
calculated by means of 'trityliZatiord " (hatodom
tritilirovaniya) (table 2). Inithe reaction of
cellulose with Na-isoamylate and subsequent methylation
the secondary hydroxyl groups have a greater reactivity
than the others. The aver"-e zYmber of methoxyl groups
per- secondary carbon atom exceeds *that of the methoxyl
groups at the primiLry carbon a-tom. by the 2-6-tines.
There are 2 tables and 6 referonces, 2 of which are Soviet.
ASSUCIATION: Moskovskiy tekstillnyy institut
(Moscow Textile institute)
SUBMITTED: January 17, 1957
Card 3/3

LINI-TAN' [Lin-Taji3;LwaRYITSKAY&, V.A.; ROGOVIN, A.Z.
4
Development of mothods for V.-to synthesis of calilljoso esters with
n-subati-tutea amino acids. Vysokom.aoed. I no.1:157-161
in 159. (MIRA 12:9)
1
L, l4nekoveMy toks til:rw~ inatitut.
(CellUl BS) (Amino acids)

suN'-Tug [Sun-Tlung]; DMWITSKAYA, V.A.; ROGOVIN, Z.A.
Synthesis of new cell4lose derivatives and other polyeaccha-
rides. Part 2: Synthesis of amino acid amidos of alginic acid
and carboxymetbylceillulose via ainino acids. Vysokom.soad. 1
no.8:1178-1181 Ag 159. (MIRA 13:2)
1. Moskovskiy tskstil'W institut.
(Alginic toid) (Cellul-ose) (Amides)

301 TUN; DMrVITSKAYA, V.A.; R=VIN, Z.A.
S3rnthesis of now derivatives of cellulose and other PDlYgaccharides.
Part 3: '5ynthesis of a graft copolymer of carboxymethyleelluloi3e
and polyananthamide. Vysokom.soed. I no.11:1625-1629 N 59-
(14IRA 13:5)
1. Moo)coveldy tekstillnI7 -institut.
(Hotatamide) Oellulose) (Polymers)

PHASE I BOOK EXPLOITATION
SOV/5286
Strepikheyev, Aleksandr jkleksandrovich (Deceased), and Varvara
Andreyevna Derevitskaya
0snovy khimii v-jsokomolelculyarnykh soyedineniy (Principles of the
Chemistry of High Molecular Weight Compounds) Moscow, Goskhimiz-
dat, 1961. 354 p. Errata slip inserted, 15,000 copies printed.
Ed.: A. A. Rogaylina. Tech.. Ed.: V. V. Kogan.
PURPOSE: This textbook Is intended for students in schools of
higher education. It may also be used by specialists In the
manufacture of plastics. chemical fibers, rubber, textiles,
and leather.
COVERAGE: The textbook deals with the chemistry of high molecular
compounds. It includes basic data on polymer synthesis, the
mechanism and kinetics of' polymerization and polycondensation
processeso and the properties and chemical conversions of
natural and synthetic high molecular compounds. Professor
Cardz,l/~8

Principles of the Chemistry 'Cont.)
k
SOV/5286
G. L., Slonimskiy wrote Part III, the section on the physico-
chemistry of high polymers. The authors thank Professor
V. V. Korshak, Corresponding Member-of the AcacLemy of Sciences
USSR; A. It. Pravednikov, Ye. A. Vasillyev-Sokolov, and M. P.
Zverev, Candidates of Chemical Sciences.; Professors S. M.
Skursttov and Z. A. Rogovin; and A. V. Volokhin, R. N. Martsin-
kovskaya, and Z. Ye. Krinskaya, Candidates of Technical Sci-
ences. Rererences accompany most of the chapters.
TABLE OF CONTENTS:
Foreword
PART I. INTRODUCTION 7
Ch. 1. High Molecular Compounds and Their Importance 7
Ch. II. Basic Concepts of the Chemist:r-j of High Molecular
Compounds 16
Caitd,_2/8

PHASE I BM KOLOITATION SOV/4984
International symposlus aq, macrosolocular chemistry. Moscow,
1960.
XszWun&rv4nTy simpozium po makromolekulyarnoY khImil SSSR.
jbakva. 1-18 0 9. ; doklady I aytoreferaty.
Soktalya 111. if-I.Y.L.2tonal Symposium on Xacrox,olecular
CZwAstrjr Hold In Moscow, June 14-18, 1960, Papers and
SmmmarLes) Section 111. [Noncow, XZd-vo AN SSSR, 19601
469 V. 55,000 copies printed.
Tech. Zd.. P. S. Kashlna.
Sponsoring Agency: The International Union or Pure'and Applied
Chealstry. Commission an Chemistry.
PURPOSE: 7his book in Intond6d for chemists Interested In poly-
merization reactions and the synthesis of high molecular
Q
r1\
X
DO,
>
compounds.
<
carsmazz van is section irl or a ciultivolume work contain-
Ing papers on jameromalocular chemistry. The articles In
general deal with the kinetics of polynerIzation reactions,
the, Synthesis of special-purpose polymers, e.g., Ion ex-
change rosins, sealconducco- materials, *to., methods of cat-
alyzing polymerization reactions$ properties and chemical
interactions of high molecular materials, and the effects of
various factors on polymerization and the degradation of
-high molecular compownds. So personalities am mentioned.
Reforences given follow the articles.
_Mev, andR. S. ?Illjxrr- (USSR).
The Radiation KetE-o-d-o-f-Coi~-ol-ymerizf-ng.Aer7lmit-ile With
-Polystyreme and Perchlorovinyl 170 i
Raflkov S M 2-A-C2111-3- I V Zhuravleva and P N
wtyitf~h oxyethyLatlon cC ft-r
---___ch,1- Polyamide; 18 4
Santa X knd K. 0*1 (Hungary). Grafting YAt.1,yl Methacr7la
5iFQ__7k__" or FFjyfj-n-yj AlcDhOl Un4or the Action of X_R&ym t:07
H, Radc, and Yu. P3vlft ti (Czechoslovakia).
ethyl KethaerrI-1-te Onto Polypropylene and Poly-
ethylene
(USSR).
r C Irto3ql -Con t;tlnfng Z~Ata.dlene-styrene
224
XQ29Znlkax_.a_A., and To'eng Ran-laing (USSR)~ Synthesis
B., and'X. Lazar (Czechoslovakja).
The Role a,- the'
-3curce of Free Radicals on Croselinking In Polyethylen a
Naadenow A. Tutorskjy, and B. A. Dcgidkln (USSR).
5? EHe irkansfd-Oma bans o.~arbcxyI-C-OnT`a_rnIng mtadlene-
Styl-ne Rubbers and ThaLr Mixtures With E~_aprclactam
Under the Action of Ga=a Radlation 293
RogovI 'nr, Chnng Wel-
. Sun T'C
.4.-Derevit
012g_r_31akfA~
an
~kn U a Syntheala of New
Cellulose grittj ther Polysaocharlde3 302
TE*rrno mX2 -I-- ., and F. K. X_Aputs~~(U33R). initiation
g1t 16 Cellulaeas With
t 11
2 0 Cantralle, Synthen 0
de: . n ra d
Z~l r Nitrogen 310
X. Ta. Lenshln2,CV:1,1., .1,,ranL.Qji (USSR).
r- ___ - . . C 1
OxIdational Trans ormatiors7n h ulose Molecules 321
Berl Ye. A. Penakayaj and G. 1. Voli~W (USSR).
anT-%1=ocdcpQlymerIZ&-
tion During the Preetlng of Starh Solutions 334
Vt52jl2y__j2j_U_ B f~ AZkhcd=h,,",y, and U__AZ_1Z2.~(USV).
hj__F over
tien
Xodlrlcation of the ropertles or cellulose by Grafting 344

POLTAKOV, A.I.; 1Dm4y1T_SK_AT4,_.V,A.; ROGOVIN, Z.A.
Investigation of the,possibility of preparing unsaturated com-
pounds of cellulose by the Chugaev reaction. Vysokom.
soed. 2 no. 3:386-389 Mr 160. (Mal 13:11)
1. Moskovskiy tekatiltayy institut.
(cellulose)

SUVI TLIN C.' 3all Tlungjj MWLT�!;~Y--A,- V-.A--,-, ROGOVIII, Z.A.
,:~,rnthesjs of now cellulose derivatives and other polymaccharides.
Part 8: synthesis of cellulose esters of amino acids. Vysokom.
soed. 2 no-5:?85-790 MY 160. (141BA 13: 8)
1. Moskovskiy takstil'nyy inotitut.
(Amino acids) (Cellulose)

S/1%60/002/012/002/019
B017 B055
AUTHORS: Sun' Tun, Derevitska-va, V, A Rogovin, Z. A.
TITLE: Synthesis of New Derivatives of Cellulose and Other Poly-
saccharides. IX. Synthesis of kromatic Amino Acid Esters of
Cellulose
PERIODICAM Vysokomolekulyarnyye soyedineniYa, 1960, Vol. 2, No. 12,
PP- 1768-1771
TPRXTt The authors developed a method for the synthesis of arcmatic amino
acid esters of cellulose. The synthesis of these cellulose esters is
carried out in two stages, i.e.
1) FC 6H702(OH)31. + XCICO C~ N.02 + x
Card 1/3

Synthesis of New Derivatives of Cellulose and S/190/60/002/012/002/019
Other Polysaccharides. IX. Synthesis of B017/BO55
Aromatic Amino Acid Esters of Cellulose
[C6R7 02(OH)2O-i-