SCIENTIFIC ABSTRACT ARIENT, J. - ARIFKHANOV, U. R.

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• Collection: Scientific Abstracts
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• Publication Date: December 31, 1967
• Content Type: SCIENCEAB

T 1) A;- i r r 'T I T T 1
ic Chemistry.
Abs Jour: Ref Zhur-Khimiya, No 23, 1958, 77614.
Author : Arient. T. and Dvorak, J.
Inst :Not given.
Title :Triphenylmethane Dyes. II. The Introduction of
a Triazole Group Into the Triphenylmethane Skel-
eton.
Orig Pub: Chem Listy, 52, No 1, 109-115 (1958) (in Czech).
Abstract: When (p-(CH 3)2 NC6 H4)2 CHC6 H4NH 2-P (I), ob-
tained in 95% yields by the condensation of
p-aminobenzaldehyde with dimethyaniline (II), is
diazotized followed by alkalinization with
OH3 COONa, reaction with /,~-naphthylamine (III)
in neutral medium, stirring for 3 hrs, alkalini-
Card 1/9
16

CZECHOSLOVAKIA / Organic Chemistry. Synthetic Organic G-2
Chemistry.
Abs Jour: Ref Zhur-Khimiya, No 23, 1958, 77614.
Abstract: zation with NaOH solution, stirring for 2 more
hrs, and heating to reflux temperature, a 100%
yield of (p-(CH 5)2 NC6 H4)2 CHC6 H4N t NR-p is
obtained in which R = 2-aminonaphthyl-1 (IV), mp
215-2160 (from alcohol). The oxidation of IV with
(CH3 COO)2 Cu (refluxing for 2 hrs in pyridine sol-
ution) gives a 97% yield of (p-(CH 3)2 NC6 H4)2
CHC6 H4 RI-P M, where RI = /)' -naphthotri-
azolyl-2, mp 212.5-2150 (from benzene). The oxid-
ation of a solution of the diazonium salt of I by
1% aqueous suspension of Pb02 (15 min, 0-100) in
acid medium followed by preceipitation of the Pb
with dilute H2 S041 filtration of the PbSO, addi-
Card 2/9

P
k~ h C, 31, U, IV'. In rk, Q
Z3 t rv. yiithjtJo ~r6alio
Chemistry.
Abs lour: Ref Zhur-Khimiya, No 23, 1958, 77614.
Abstract: tion of GH3 COONa, reaction with III and treatment
similar to that used in the case of IV, gives 94%
yields of (p-(CH3). NC6 H4)2.C(OH) C6 H4 N = NR-p
(VI), mp 202-2040 (decomp), which is purified by
reprecipitation from acid solution or by precipi-
tation from dioxane solution with water; as an
alternate method precipitation with benzene from
petroleum ether solution can be used. The 6xida-
tion of V with PbO2, followed by the salting out
of the carbinol which is-pnoduced, refluxing of
the latter in alcohol, dilution of the filtrate
with water, and alkalinization with NaOH yields
93114. (p-(CH 3)2 NC6H4)2 O(OH4 RI-p (VII, Mp 179-
179.50, which is purified by precipitation with
Card 3/9
17

CZECHOSLOVAKIA / organic Chemistry. Synthetic Organic G-2
Chemistry.
Abs Jour: Ref Zhur-Khiaiiya, No 23, 1958, 77614.
w
Abstract: C6 H. from petrolebm other. VII can also be pre-
%J
pared in 92% yields with the oxidation of VI by
a procedure similar to that used in the prepara-
tion of V, The diazotization of 0.03 mol para-
leucoaniline (VIII) in the presence of KBr, fol-
lowed by reaction with 0.1 mol III and treatment
similar to that used in the case of IV, give 96%
yields of (06H5)2 CHN = NRII-p (purification as
in the case of VII) which is oxidized by a_Rroce-
dure sisailar to that used with V to give qq~b
yields of CH(C6 H 4RI-P)3 (,X)9 MP 206-2080 (after
drying for several days at 1100 in vacuuo); fol-
lowing precipitation from benzene solution by the
addition of pBtroleum ether, DI is found to contain
Card 4/9

CZECHOSLOVAKIA / organic Ghemistry. Synt.1-lietle ~;rganlc U-4
Chemistry.
Abs Jour: Ref Zhur-Khimiya, No 23, 195B, 77614.
Abstract: 1 mol 06 H6* By a procedure similar to that used
in the preparation of VI, the diazotization of
VIII, followed by oxidation with PbO,,, and re-
action with III yields 98% HOC(O 6 H4 N = NR-P)3
(purification as in the case of IX); the oxida-
tion of the latter product for 4 hrs by the pro-
cedure used in the case of V results in a 94%
conversion to HOC(C 6 H4 RI-P)3 (purification by
chromatography on Al. 03). The acetylation of
(p-NH 2C6Ht)2 CHC6 H5 (XI) (H. Weil and co-workers, Ber,
61, 1294 1928)) by heating for 2 hrs with (CH3-
00)20 in CH3 COOH over a water bath, followed by
Card 5/9
1e

CZECHOSLOVAKIA / Organic Chemistry. Synthetic Organic G-2
Chemistry.
Abs lour: Ref Zhur-Khimiya, No 23, 1958, 77614.
Abstract: the addition of 33% HC1, oxidation by Pb02 (15 min),
precipitation of the aoetyl carbinol with water,
and hydrolysis of the acetyl caibinol by heating
for 10 min with (1:2) H2SO4 to 110-1150 gives a
78% yield of p,p'-diaminotriphenylearbinol (XII),
mp 173-1740 (from C5 H5 N). The reaction of dia-
zotized XI with III gives a 100% yield of C 6 H 5
CH(06 H4 N = NR-p) 21 mp 159-1610 (purification as
for X); the oxidation of the latter product by
the procedure used for V gives a 96% yield of
C6 H5 CHN 6 H4 RI -P)2 (XIII), mp 149-1510 (puri-
fication as for X). The reaction of diazotized
XII with III gives an 86% yield of C6 H 5 COH(C6 H4
Card 6/9

CZE-WHICSLOVAKIA Organic Ghedai-itf Y, QyiILLt-'L"~
Chemistry.
Abs Jour: Ref Zhur-Khimiyal No 23, 1958, 99614.
Abstract: N = NR-P)21 mp 118-1220 (purification as for X);
when the latter product is oxidized by a procedure
similar to that used in the case of V, C6 H5 COH
(Cr, H4 RI-p)2(XIV) is obtained, mp 182-1850 puri-
fication as for X). The reaction of diazotized
p, pl-diaminodiphenylmethane with III gives 99%
yields Of CH2 (C6 R4 N = NR-p)21 mp 224-2250
(from o-dichlorobenzene); the product is dissolved
in pyridine, and the solution is added over 8 hrs
to a boiling solution of (GFi3 COO)2Cu in pyrid-
ine, the mixture is poured into water giving a 96%
yield of CH2 (C6 H4 RI-p)2 (XVI) Zs`i_c7' mp 314-
3160 (from o-dichlorobenzene). Attempts to oxid-
Card 9/9
19

CZECHOSLOVAKIA / Organic Chemistry. Synthetic Organic 0-2
Chemistry.
Abs.Xour: Ref.Zhur-Khimiya, No W,,1958, 77614%
orkesponding carbinol or to
Abstract: ize:)dr_fB_ic7 to t~e 6
the benzopFienio'A'q~deiivative were.unsuccessful.
Similarly the reaction of diazotized pt pl-diam-
inobenzophenone with III gives 98% yield of
000 6 H4 N-~-- NR-p)2, mp 275-2760 (from o-dichloro-
benzene); oxidation of the latter product by a
procedure similar to that used with XV gives 94%
OC(C H Rt-p)? (XVI) Z_sij, mp 318-319u (from
6 4
o-dichlorobenzene). Attempts to effect the con-
densation of XVI with II in the DrOsenee of POU 3
or to carry out a reaction of XVI with chloroben-
zene in the presence of Na were unsuccessful. The
above-described tripheny1methane derivatives con-
taining the triazole ring when dissolved in organic
Card 8/9

CZ/8 -52 (82 -10-18/39
OTHORS: Arient, J and Franc, J.
TITLE: Derived FroM ImidazoI4. I. (Imidazolov b1wiva.1)
T Dyes
Fireparation and: uhromato3raphio Separation of yes From
1,4~,5pS-Naphthalene Tetracarboxylic and 1,8-Naphthalene
Dicarboxylic Acids O?Rprava a chromatograf IckEf d4le~f
imidazolovy'oh barviv z 1 4 5 B-naftalentetrakarbonove a
1,8-naftalendilcar:bonove',~y'seiiny)
WRIODICAL:, Chemick6 Listy, 1958, Vol.52(92)., Nr-10, pp 1946-1950
(Czechoslovakia)
ABSTRACT: The authors repeated the synthesis of napht4oylene-bis-6,
61-ethoxybenzimid4zole dnd. naphthoylene-bl~i..c(,O('-naphth -
imidazole The authors synthesised naphthoylene-6-ethoxy-
benzimada;olep naphthoylene-et-naphthimidazole and naphthoy-
lene-peri-nAphthimidazole. Properties of all these com-
pounds are given In Table 1. By paper chromatography the
authors succeeded In.separating the dyes into their various
'ormation of theoretically
components and to prove the -L
possible isomers (Table 2). From the colouration of the-
various Isomers it was possible to conclude that the iso:-
mers with carbon.*L~~,groups in the 1 or 1-4 positions
absorb on longer wave len~gths than the isomers with
Card 1/2 carbonyl groups in the 8 or 1 and 5 position. The fluores-

Dyes derived from ImIdAzole. H. Manoaroyleneladds-
zole_41eederived from tatramines of the benzene series.
V Ffu-tnnd J. Marlum (V�zkum. fistay pfg.jy Par-
+61-111"Ryb1tv M7eWj-oi-M-eX5_srW RIM...'Com-
,tinins. 25, 1114 INY1 In Gertuan); cf. C.A. 53, 11912e.-
'.fit contrust to Fr. 1, j 15 (C.A. 33, MI&O, condenmition
'Of I.8-C,.If.(CO6H).IV1) with syns-C.If.(NIf,),, tetra-
~ICI salt (111) gave (R RI - NHAc) V,21~ and a
0
C-11
C
(IV)
small amt. of IV (R H. R' - NllAc) (V) and IV (R 11,
R' OAO Mi. The unsubstituted I,2AIA)qi:iphthoyI-
cliebenzimidazole, IV (R - R' - H) (VII), was obtained as
one of the by-products in the condensation of I with I'&
dininhux-1,0-dinitrolienzene (VM) followed by redn. of the
nitro groups. Adding with agitation diazotized 70 g. Sul-
fanilic acid and 60 ml. 15% aq. NH, to keep. the pH at
7-7,15) to 83.3 g. jV,N'-I)is(,&-toluenesulionyl~iii-plienyletie-
diamine, 10 g. NaOll. M nil. HtO. and 400 K. crushed tee,
Stirring the nilit. I fir., heating to 60% acidifying with 100
ml. coned. HCl, filtering off the ppt., and washing %vith clil.
off. HCI gave a diazo dyc (free of the niononzo compd. as
shown by chromatography of its N114 salt on Whatman No.
J paper with 1*1:1 AmOH-C.H.N-aq. NH.): treating
thadyeportlonwiseat the b.p. (in 1000 ml. HjOand M ml.
45(,',0' aq. NH.) With 130 g. Nla,,%O,, filtering the ppt. hot,
and iv;~sliing with 200 mi. H.0 gave 67.3 g. 1,5-bis(Ptolu-
'eA, enesulfonanti(iii)-2.4-(Iiaiiiiiiobenzene, white tablets. in.
7-, 2280 (MOH). DbLewlying this (44.05 g.) with ngitation lit
40ft ml. 80% IIISOI, Slowly heating the snin. to 140', stir-
16P1. Y, 'ring Aj)tjkn.., atyl keeping j (lay qt room Acipp..,pye lustrous
Ituflet- of 2H.3113SOl; the- filtrati deposited afi&'3'days
-whitencedlest)(11.1-1,S0s. Treating the mixt, of lite above/
sulbites with 200 mi. coned. IICI at 70* 10 inin., filtering
off the pit.. iind reliptil. with coned. HCI front ou aq, Solo.
gavel9.ljt.Ul. Boiling 10 lire. 14.2 g. M. :Mmi. AcOll.
and 21.6 g. I and cooling gave 29.2 g brown ppt. which
was washed with 30 nil. AcOH and bojW with 5 g. NajCOi
aud250mI.HO. Filtering while hot, washing with 100nd.
1110. and drying at 80* gave 18.7 g. brown. cryst. powder
(acidification of the filtrate yk-lded excess 1) which was
chrotuntographicil on Ali% (activity 1). B(WL%-Ave clution
with PhNO., EtOAc; and 1:1 CaUrcyc"exanol gave
V, and (as the chief product) Wit, purified by 1) tn. from the
CH,N soln. with petr. ether, yellow powiler, insol. -in
CHC4. CC14. and CS.. Sol. lit coned. lfSO~: infrared
spectrum given. Adding "ionwise 12 g. Fe powder and
5 nil. coned. IICI to a boiling tnixt. of 200 nil. AcOll, 3 g.
VUL and 6.5 g. 1. refluxing 16 hri., filtering hot and working
up gave 5.45 g. Mi, chromatographically identical with that*
obtalnedfromM. Refluxitig2hrs.0.2g.2,4-(OsN~CIl~
NHj, IOS g. 1. and 150 ml. AeOll, adding portiotiwisc 30 S.
Fe pow&r and 5 ail. coned. IICI, refluxing 9 firs., cooling,
filtering off the paste, washing with hot uq. HCI and then
hot aq. NaCO,, und drying gave 3.25 g. brown powder;
an addid. 10.15 g. was obtained on pp(g. the AcOll filtrate
with Hit). Chroniatography c( lite couthfued product mi
Ali (-fivll -.1ution with Mile gave a yellow-
1), and t
tu. approx. 215* (constitution not detd.)
r
to
ycfl.~ powder. in. 232-3* (purified by ppin. with
petr. ether front the C&II&I solu.); successive eluilon with
ClIC4 gave V, orange powder, in. 2(W (purified as VI).
Chromatograims on Whatinan No. I paper (clution with 3:1
cyclobexane-Call,N) showed the following R1 values and
colors of fluorescence- lVa 0.25. yel6w; V. 0.45, yetiaw-
orangL; VI, 0.0, green; 1, 0.73, violet; and VII, O.M,
yellow-green. A similar prowture was used tit prep. lite
impure 7-Ale deriv. of IV& from 3.6-bis(plienylazo~2,"ia-
ininotolucue jili Mild

Betuoylottion of OS&f Ane and liILLI_nthap.
fi-Mi 5
dd
In
b: 1 0
d t
94
289
F
C
h
f
o
. ago o
a
e
e
zec
.
.
,
pyrtne 101 In dry o-dichloraberizene 050. the alixt. treated
wtth small regular doses of anhy-d. 4UC14 In the cour-te of I hr,
(total 200) so that the temp. did not exceed W. tht: mixt.
stirred 5 lira. until the temp. has dropped to 45' and then
12 ftddnl. hrv., the brown-red "spension poured into HjO
WO and a
rter the dcLompn. of AICL has ceased (qpontanc-
I
Ous warruing to 7()-8u*) the Mixt. steam-distd. gavc LL Ycl--,

ARIENT, J.; MARHAN, J.; TAUBLOVA, H.
Imidazols dyes. III.Reaction of sym-tetraaminobenzene vith carbMlic
acid. Coll Cz Chem 25 no.6:1602-1611 -Te 160. (EM 10:9)
1. Forsobungsinstitut fur organisehe Synthesen, Pardubiee-Rybit7i
und Technische Hoehschule fur Chemie, Pardubice.
(Imidazole) (Dyes and dysing) (Amino group)
(Benzene) (Carboxylic acids)

RATRIKA, Miroslav; SAGNM, Zdenek; STERBAs Vojeslav;-A~i ~Tl -T~ollef
Decomposition mechanism of some basic tripherqlmethans d7es in
aqueous medium. Chem prum 11 no.11:571+-577 N 161.
1. Vyzkumny uotav organiolcych oyntez,, Pardubice-Rvbitvi.

ARIMT., J.; MARFIAN, T.
Isidazole dyee. IV. Consensation of o-pbonylenediamine with phtbwlmm
bydride. Coll Cz chem 26 no.1:98w-106 A 161. (Eui 10:9)
1. Forachungainstitut fur organisehe Syntheaen, Pardubice-Jlybityi.
(imidazole) (Dyes and dyeing~ (Phenylenediamine)
(Phthalan

MATRKA, M.; NAVRATIL, F.; STERBA, V.; ARIENT, J.
Polographic determination of 2,21-bia-pyrazoleanthrone in the
presence of py zoleantrone. Coll Cz Chem 26 no.7:1763-1767 11 161.
1. Organisch-technologisches Iaboratorium I,, Forschungainstitut fur
organische Synthesen, Pardubice-Fqbitvi.
(Anthrone) (Pyrazole)

ARIENT, J.; MARHAN~J.
Pyrene derivates. Part 2: Production of polycyclic quinones
from pyrenes. CoU Cz Chem 26 no.8:1941-1948 161.
likl~orscbungsinstitut fur organische Synthesen, Pardubice-
Rybitvi.

4 P I t~ AJ T, J.
SUMAME.. Given Names
Country: Czechoslovakia
Academic Degrees% Lnot gived
Research Institute of Organic Synthesis (Forschungsinatitut
Affiliation: fuer organische Synthesen), Pardubice-Rybitvi
Source: Prague Collection of Czechoslovak Chemical Communications,
Vol 26: No 11, November 1961, pp 2774-2780
Datas "Imidazole Dyes, VI. Synthesis and Properties of
1,2-Naphthorlbensim'dja ole."
Authorst
J
ARIENT, J
V'~

KOUTECd, J; ZAHRADEA, R; ARIENT, J.
Czechoslovakia
Institute of Physical Chemistry, Czechoslovak
Academy of Sciences - Prague; Research
Institute 9f Organic Syntheses -- Pardubice-
Wbitvi ^11
Prague, Collection of Czechoplovak Chemical
Comma-Hro-Trons, Iro Tr,-Zrr, pp T4F6::M3
113tudy of the Relations between.the Physical
Properties of Symmotrioal! Quinones and their
Structure on the Basis of,;tho UG-LCA0 Uothod."
OWN== ww- HE-

KOUTECKY, J.; ZAHRADNIK, R.; W-'TT-.!-J--
Vxamination of th e relations between the,.phyBical properties of
symmetrical quinones and their structure~by the HO-WAO method,
Col.1 Ca Chem 27 no,11:2491-2515 N 162, 1.
1. Institute of Physical Chemistry, Czechoslovak Academy of
Sciences, Prague and Research Institute of Organic Syntheses,
Pardubice - Hybitvi.

CZECHOSLOVAKIA
ARIENT, J; MARHAN, J
Research Institute of Organic Synthesis, Pardubice~
Hybitvi (for all)
Prague,.Colleotion of Czechoslovak Chemical Communi-
cations, No 5. 19639 PP 1292-1300
"Imidazol Paints VII. Condenwition of 1,8-Napthal
Acid with 1,2-Diaminobenzol-.Der:Lva-tea."

CZECHOSLOVAKIA
ARIENT, J; HAVLICKOVA, L.
Research Institute of Organic Synthesisq Pardubice-Rybitvi
(for both)
PragueI Collection of Czechoslovak Chemical Communications,
No 7, 1963, pp 1865-1893
"Imidazol Paint VIII. Reaction of Substituted Phthalic
Acid Anhydrids with 1,2-Diaminobenzol.11

16
CZECIIOSLOVAkIA
ARIENT, J; DvbRAK, j; SNObL,.D.
Research Institute of Organic Synthdais (Forecliungainatitut'
fUr organische Synthesen), Pardubice-Rybitvi (for all)
Prague, Collection of Czechoslovak Chemical C*ommunications,
No 9, 1963, pp 2479724B9
"Imidazol Paint. X. On'the Condensation of-2,6- and 2,7-
Dichlornaphthaline-1,4,5,8-Tetracaronic Acid with o-
Phenylendiamine.11

CZECHIOSLOV.4KIA
ARIE11T, J; '11-ANILICKOVA, L.
I-
Research Institute of Organic Synthesis (Forschungs-
institut fiAr organische Synthesen), Pardubice-Rybitvi
(for bo-uh)
Prague, Collection of Czechosloak- Chemical Communications,
No 9, 63, pp 2534-2536
"Imidazol Paints.XI. On the Condesation of Pyromellith
Acid vvith o-Phenylendiamin."

MARHAN . J.
Imidazole dyes. Pt. 7. Coll Cz Chetft 28 no. 5: 1292-1300
My 163,,
1. Forschungs' Institut fur organische Synthesen, Pardubica-
Rybitvi. 11

ARIENT, J.; IIAVLICKOVA, L.
W-Man-Mr"If 1.
Imidazole dyes. Pt.8. Coll. Cz Chem 28,nd.7:1885-1894 Jl 163.
1. Forachungainstit4t fur organische Synthesenp Pardubice-
Rybitvi.

ARIENT, J.; DVORAK, J.; SNOBL, D.; HAVLICKOVA, L.
Imidazole dyes. Pts. 10-11. Coll Cz Chem 28 no.9:2479-240,0,
2534-2536 S 163.
1. Forschungsinstitut fur organische Synthesen, Pardubice-
Rybitvi.

ARIENT, J.; MARHAN, J.
`~---.. p -
Imidazole dyes. Pt. 12. Coll Cz Chem 28 no. 12;3352-3361
D 163.
1. Forachungsinstitut fur organische Synthesen, Pardubice-
Rybitvi.

ARI&NT, J.; DVORAK, J.
Pyrene derivatives. Pt. 3. Chem prum 14 no.7:357-359 J-L 164.
1. Research Institute of Organic Syntheses, Pardubice-Rybitvi.
.2 1

ARIENT, J o s ta f
"Symiaptio organic dye-; arij thpir int,errapWAte products" by .11.R.
Schwaitzer. Raviewed by Josaf I-rient. Chem prum ll~ no.12:&731-.
6174 D t64
1. Rese&rch Institute of Organir; Syntheses, Farciubice-Hyb1tvi.

ARIENT, J.; BAVLICKOVA) L.; -SLOSAR, J.
Im-idazole dyestuffs. Pt. 13. Goil Cz Chem 29 no.12;3115-312-' D 164.
.1
1. Forschungsinstitut Dir organiadhe Synthosen, Pardubice-Ptrbltvi.

CZECHOSLOVAKIA
ARIENT,J; DVORAK, J; NEPRAS, Y,; OEM, P.
Research institute for Organic Synthesis, Pardubice-
Rybitvi (for all).
Prague, of Cze&1o3lovalk Chemical Cormuniort'tions,,
No 11, lk~'oveimber 1965.,Pp 37J.6-3729.
"Imidazol dyes. Part 15: Pr8sentatiOr. of arolyleni-midazol
dyes and the influence of substitution on their coloring
properties."

AR-1---
CUMMIMAUA
noww"m lasum" ur cmeau gynthwif,
Cw oqwdnbp OpAhwmjv PAWM440.1-vu"i (I" boa)
vramwo fdalwa 29 UUWI=b CbwAoM isommAub xv 3*
Joamoy 19"s vp W-an

mamo vj
Researob InotItaft for Oramle Slatbsole Voraobur*s-
laskitulk AV 01-puldebe 3jntb*9*n),% Pardubleowfilb1tvi
r"Per callall at gmbaAlwx ghmigol 92makw
lag=& so 50 xa"h 1'9tpb* pp 1093-1100#
Oluldowle 4yes. ftrt 171 NitntIca of 2-**waylbmzicd-
desole and Its n1tro derlTatlTo**fx

CZEU- UOSLOIJ;~:UA
M; ARIENT, j; KOUTECKY, J
I. Institute of Physical Chemistry, C-zachoslovaI.' Acadoz,-,y
of Scieneas, Prague (for Zahradnik and Koutocicy): 2. RQsoarah
Institute of Organic Syntheses, Pardubice-Rybiuvi (for Napraa
and Arient)
Prague, Collection of Czechoslovak Chemical Cornunications-,
No 3p March 1966, pp 118o-1168
"Imidazole dyes. Part 13; Electronic speot.-a and reactivity
of imidazole dyes."

CZECHOSLOVAKIA
ARIEVT, J; HAVLICKOVA; 19TIMM, J
Research Institute of Organic Syntheses, Pardubice-
Rybitvi - (for all)
Prague, Collection 9-f Czechoslove-It Chemical Connun-i-
cationso No 120 December 1966, PP 4682-4693
M
"Imidazol dyes. Part- 19: On the reaction of 1,,2-ben-
zoylene benzimidazole and 1,,2-naphthoylone benzimidazole.11

ARIENT, Jcsef; DVORAK, Jan; IT.111S, Petr
Oxidation of naphthoylene-bis-benzimidazoles. Chem prum
13 no.5:245-246 My 163.
1. Vyzkumny ustav organickych syntez, Pardubico - Rybitvi.

LXGh-1-RFTA V~IDIGA Sec 16 V01- 5i1Z Ca---cer L-zc- -5-1
4462. DIENSTBIER Z ARIENT M. and KOFRANEK V. 1. Clin. of Intern.
M"1 L
Mcd., Charles Univ., Ccntra ab., M Hosp., Prague; Dept. of Oncol., District
Hosp., Usti nad Labern On the mechanism of early leukocyle changes in rats after extensive
X-irradiation. IV. Influence of partial irradiation Neoplasma 1957, 4/1 (15-20) Graphs I
Tables I
The total number of Icucocytes in 2 groups of Wistar rats irradiated with 700 r.
(200 kv.) on the head and chest, and on the abdomen, showed a significant decrease,
both ncutrophils and lymphocytes being affected. A third group of rats rcccivino,
the same dose to isolated 'Intestines after laparotomy did not show this dccrcasc, buot
rather a slight neutrophilia. A control group of laparotomizcd rats that received no
radiation showed a marked neutrophilia. It is concluded that the extent and rate of
decrease, articularl~'of lymphocytes, following X-irradiation are directly propor
tional to tte sizc of t. e irradiated area and do not depend n the site irradiated.
Men - Johannesburg

AFdE_NT' IM.
DIENSTBIER, Z.; ARIENT, M.
Mechanism of changes of leukocyte count folloding,.lethal roentgen
irradiation. III. Effect of tissue homogenates. Gesk. fysiol. 6 no.l:
6o-66 157.
1. Technicka spoluprace; H. Spankova, H. Mlejnkova. 1. Ploticova I.
klinika chorob vnitrnich KU, Praha, UZL, UVN, Praha Statisticke
zpracovani: V. Maly, Ustav pro organisaai %dravotnictvi. KU, Praba.
(R03HTG3K RKM, effects,
lethal dose on leukocyte count, off. of tissue homogenates
in rate (Cs))
(LIUKOCYTI COUNT, affect of radiations,
x-ray lethal dose, off. of tissue homogenates in rats (CZ))
(TISSUB 3XTRAOTS, effects,
on.leukocyte count after lethal x-irradiation in rate

PARIZEK, J.; ARIENT, M.-O DIENSTBM, Z.; SKDDA, J.
Mechanism of poot-irradiation desoxycitidinuria. Cesk. fyaiol.
8,no-3:2.30 Apr 59.
1. laborator pro fysiologii a --Datofysiologii premeny latek CSAV,
Vyzl,mmv,v ustav hygieny, epidemiologie a mikrobiologie, J~rsikalui
ustav fak. vaebb. lek. W, Cheinicky uBtav GSAV, Praha. Predneseno
ne. III.fysiologickych dnech v Brne due 15. 1.1959.
(NUCLAOSIM AND NVOLEOTIMS. in urine,
dasoxycitidine in %-irradiated animals (Gz))
(ROENTGEN RAYS, eff.
urinary desocycitidine in irradiated animals (Cz))

DIZNSTBDM, Zdenek;KOFRAM, Vladimir; BROUS IL, Jindrich _ ISNT, Mir-o8jav (Tech-
nicks. spoluprace: J. Jasan, Statisticks stre1&-,4dd--Prah&)
Statistical st-adlies on health and fertility of physicians working
with ionizing radiations. Ges. rentg. 13 no.5--330-342 0 159
(R&DIA6TION MFECTS)
(MTILITY radiation effects)
(PHYSICIANS) -

PAZ:EZEKp I.; Attag X.; DUNSTbIlM0 Z.; SKODA9 1.
Ixoretion 6f desaxycy-tidine in the urine after irradiation as
an early test for radiation injury. MeA.rad. 5 no.,301-38 1~0.
(M3RA 1302)
(DEOXYGYTIDM) (RADIATION SIMMS)

ARIENT, M.; SKALA, E.; POTMESIL, M.; PALA, F.; DMK, V.
On the treatment of acute leukaemia by massive whole body
irradiation combined with subsequent bone marrow transfusion.
A case report. Neoplasma,Bratiol. 7 no-3:295-3o4 16o.
1. Military Institute of Hygiene, Epidemiology and Microbiology,
Central Military Hospital, Prague, Czechoslovakia.
(IOMMIA MYELOOTTIC radlother)
(BONE MARROW transpl)

DIENSTBIRR,Z.; ARIMT, M.; POSPISIL. J.
Nonspecific post-irradiation leukocyte changes. Cas.lek.ceek 99
no*X-33:1007-1013 12 Ag 1600
1e Biofyzikalni ustav lekarske fakulty KU v Praze. Vojensky ustav
bygieny. spidemiologie a mikrobialogie v Praze, Veterinarni
vyzkumne stredi6ko v Praze,
(LMXOCY,ZMS radiation eff.)

1 6

-~,)iwzt !,m i,n ;.i. ~f vti~ i Y-r.-i zien -IM !L~
FrAnrd'2 7), CU -'.71, Or, Iri., to.: 3
12), 0-1 1;1,~ :1%
cta,.-Iv~L; Contrpl
Ici ~L,

2rncn- ~,n c.,f th, :U01nat'-, in Mr-l'" Pro

ir, t~-~ ntrito c-f r- Ln-rva,~,l
VLAi~y., *,D, of
th,,

'
'
r
ic., !-
o Z~
itri Lf2Li~, 17 -
j pp
ir, *,~- Va,~ Lir'~tr---kni; Cc-
20n,!-, v,; ~p 20-i",
l
7. th- 'rrEL')ILr,'
oz: ti" 7f.-er.-zwn, V~,,tc- "Iel.,or:ie-rnt -;yi;

S. ric -.n v-e to '4,, v0snel
Ccltr.,;~ .'~m C-7. 1 Ytji,,r
-
Ord
C.., V!6 9":
Tfi. vni-rra ji-

of tna ~'njjrl-i w.' t:)-- -10!: Psr-b of tho
:7). of t'n" ~clvxich -~nck-ut 'I
of
fr9dittel.); P?

ARIENT, M.; KOVARIKOVA, H.; CIH&K, A.
Contribution to the determining the N-methyl-2-pyridone-5-carboxamide
in the urine of patients with malignant disease. Coll Cz Chem
27 no*7:171-1-1714 J1 162.
1. Department of Clinical L~bwFatorios, Central Military
Hospital Pragues3xud Institute of Organic Chemistry and
Biochemistry, Ciechoolovak Academy of Sciences) Prague.

SMETANA,, Karel; HERMANSKY, Frantisek; AgRL~L~ilo~.
Studies on the ultrastructure of human eosinophilic leukocytes in
peripheral blood. Cas. lek. cesk. 101 no.42:1265-1268 19 0 162.
1. Laborator elektronave mikrogkopie Vyzkumneho, ustavu experimentalni
terapie, reditel doe. dr. 0. Smahel. Histologicky ustav fakulty
vseobeeneho lekarstvi KU v Praze prednosta aka4emik J. Wo-If. Laborator
pro patofyziologii jater a krvetvorbLy pri I. interni klinice KU v
Praze, prednosta prof. dr. V. Hoenig. Hematologicke oddelehi Ustredni
vojenske nemocnice, Praha-Stresovice.
(EOSINOPHILS)

Nuclear Medicine
CZECHOSLOVAKIA uDc 612.111 /.112. 014. K8-081~
KOFRANM, V.; POSPISIL, J.; DIENSTBIEM, Z. - ARIETIT M. * Research
Institute of Radiation Hygiene (Vyzkumny Usd~~tfl-efi~;~areni),
Prague; Biophysical Institute, Faculty of General Dledicine, Charles
University (Biofysikalni Ustav Fak. Vseob. Lek. KU), Prague, Chief
(Prednosta) Prof Dr Z. DIENSTBIER; Department of Clinical Laborat-
ories at the Contral. Military Hospital (Oddeleni Klinickych Labo-
ratori Ustredni Vojenske Nemocnice), Prague.
"Dynamics of Peripheral Blood Changes in Relation to Combined
External Radiation and the Activation of Na24 in Rats. 1. 11
Prague, Casopis Lekaru Ceskych,.Vol 106, No 8, 24 Feb 67, PP
201 - 210
Abstract ZA-uthorst I~nglish summary modified 7: Dynamics of periph-
eral changes of leucocytes, neutrophils, an~d lymphocytes in rats
were investigated for 211. hours to 29 days following an irradiation
by 25, 100, 600, and 1000 R of ionizing radiation from various
sources. Lymphocytes are the cells most sensitive to irradiation.
From the change in their numbers it is possible to determine what
amount and what kind of irradiation (X-ray, gamma, neutrons) was

ARIESAN, Maria
U L RUMANIA
Professor
Bucharest, _Fnrm~ni_n~L. Ro-Usta a uniunii SocititAilor (-,,e StiintC,
-ledicale din Rem1blica Pomi-Intra llopdnp~, 'jo 9, vol ~,, som CC.,
pp 531-533.
113'_Jochemc.,~l Clizinges in "the Liver of I..Ihito P_nts tho IL-n.L-'-'uence
of Organic Dyes, Orange GGII P-nd Lmara,_,Ll, It
ull
Co-au-Urlors:
ARIE'S.Vll Fdaria, Phaimuicist.
LUNT U, G,: u
U.

I
GALEA, V.; ARIESAN, Maria; LUPUTIU, Georgeta
Biochemical changes in the liver Of albino rats under the
synthetic organic dyes# Orange G.O.N, and amaranth. Rummian
mod. rev. 7 no.W648 163,
(LIVER) (AIOCHE24ISTRy) (DygS)
(VITAMIN A) (GLUTATHIONE)

CE'untry
Category Cnemiczl Technelocry, Pbarmaceuticals. Vi-tamins
Antibiotics
Abe. Jour Ref '4hur-Khimiya, No 14~ 1959, No BOM
liuthor Mairovici, G.; Ariesan, V.
Institute
Title Vsinfecting -Pronerties of the Quaternary
Substance of Ammonia of the"Zephyrol" Type
Oripa Pub. I Farmacia (Romin.)t 1958,6, No 1, 29-36
AbstracL I Investigated were phenol nur.-ibers and bacteri-
ological action of sijbstances of t-be " Ze-phyro
t"o preparad from a raw material derived from
Iacal stearine. It is indicate-I that the syn-
thesized nubstance was found to be a good
antiseptic and may he widely used in surgery,,
genecolon,-, urelo", for sterilization of
gau-ae, and for surricaj. instruments.
--A. Vavilova.
Card-,
Co"Intry - COMMUNIST CHINA H-17
Category t Cliemical Technolopy.Pkarmaceuticals. Vita-m-ins.

AMONESCU, N.; COSTEA) L.; 4&M5M
_
Some aspects of the development of combustion process in turbulent
current. Studii cerc energet B 12 no,2:163--176 162.

ACCESSION NR: AR4015667 S/0081/63/000/021/0489/0489
SOURCE: RZh. KhImiya, Abs. 215108
AUTHOR; Arifdzhanov,__.A,.; Starodubtsev, S. V.; Sultanoy, A. S.
TiTLE: Polymerization of acrylonitrile in solutions,under the influence of gamma
rays
CITED SOURCE: Sb. Fizika I khimiya pr1rodn. I sintitich. polimerov. Tashkent,
AN UzSSR, vy*p. 1, 1962. 143-148.
TOPIC TAGS: acrylonitrile, acrylonitrile pol~merliation, dimethyl formamide,
sodium rhodanide, potassium rhodanide, polymer'tCansttion depth, finished strand
solution, gamma 'radiation, radiition polymerization
ABSTRACT: The polymerization.of acrylonitrile was studied in aqueous solutions of
rhbdanides, as wet! Ss In dimethyl'forifiamide. in order to obtain fin-
K, Na and NH4
ished strand so)pt*ons. Total transformation caq betattalned during polymerization
"'" tat doses of 4000 rad), but the solutions cannot be used directly
in such solutions
for spinning in,,vigw of their lqw gpecific viscosity. The value of &7 does not
vary with the degree of transformation. Polymerization In mixtures of dimethyl
a
gin i de d W,~tef (up to 25%)10es not lead to,increased values of characteristic-!'
f06
Eve-7- 0,3 e) Illy

7-T
POPM TA05z additlva, pOIjmrjLrabIOti7 vam-.a ray, n`~[-
mftvwx.~am peirzulSata, bh~drvgsm psT-vmide, hydroquirions, toluene, carbon totrachliwide,
---31fur, vtcetic. acld, dIvz44hjFI-Co--am-ide, azediisobutyronitrile, W~Ogallo'L#
1. was t,'-e ai-m of t~E~ at,-udly tc pro-duce higbl~r Viecmls gf-l-LI-11-cris,
% p wee tr~-a*~ed tvri-
I i t
ilia', fti-If a-Tgam-~ m. x -'%di solutl.ons -f artvtonjLum per s o
I
i A: ~rro.,-,U o1 n t. et~rar-,'-Liorlde,
'f acetic
.a rd I

AC~&5510N NHi A.F5W5262
a ed w
~A T~DN Inatitut japol.lzovenijra tDpj4v& (jM,3t;tAe of Fue_ -3 on
S~J'3 ~lj 7': T ~T
23JiAI5
~iC R&F ',:;-)V 003 HER 002
Ccird 213

!r
Dose, r
Fig, 1. Degree of transformtion as function of Uie dose of
gamm ray-s
To a 1, 2 - q + ~~-ciene ol" moric-ti-er
r
nv~ rc-quirlone; of
ion OL
Caro 3.13

SULTANOV, A.S.; AZERBAYEV, I.N.; SAFAYEV, A.S.; ARIFDZIIANOV, A.
~- I
Production of ethyl formate on calcium phosphate. Vest. AN
Kazakh. SSR 20 no.8:24-32 Ag 164.
(MM,A 17.-11)

ARIFDZHANOV, A.; SAFAYEV, A.S.; SULTANOV, A.S.
Production of ethyl formate by, the esterification of formic
acid and ethyl alcohol on aluminum phosphates. Dokl. AN Uz.
SSR 21 no.9:33-36 164. (MIRA 19:1)
1. Institut iapollzovaniya topliva Gosudarstvannogo neftekhim-i-
cheskogo komiteta pri Gosplane SSSR.

PET. VAITV, A.
APT7-T"/?PAll'l^V, 'I. A. -- IlSor~-a imlii:~4~s of Vampulnr ".--,activity in Pati-ints
With flypertonic 'js~ase ull',101' llct-Cliyral-~, Corlfl;~tj.on5.11 Tashkent
State Medl-cal Inst imeni V. 1,11. Molotov. Tashkent, l9cfr.
(Dissertation for the PeRree of Candidate in 'r-l-edical Sciences)
SO: Knizhnaya Letopist, NO 1, 199

ARnFDZHANOV, LI.* aspirant
Diffusion of Oxyurls among children and adolescents In Tashkent.
Ngd.zhur.Uzb. no.11:81-82 N 158, (NM 13:6)
1. Iz kafedry obehobey gigiyeny (zav. - prof. S.H. Bavadzhanov)
Tashkentekogo gosudarstveunogo meditsinskogo instituta.
(TA 11 --OXYURIkSIS)

ARIFDZHANOVO 1.1.9 aspirant
Rare case of a combination of the rat tapeworm w#h the dwarf ta -
worm in.children. Med. zhur. Uzb. no.8:80 Ag 160. (MIRA 137
1. Iz kaNdxy obahchey gigiyeny (zav. - prof. S.N. Babad2hanov)
Tashkentskogo gosudarstvennogo meditsinskogo instituta.
(TAPEWORM)

EMYIVTSEV, G.A.; AMFDZHANOV, K.A.
- -,::~~.--~,4ro
Producing formolvaccine against colibacillosis in sheep (lambs).
Uzb. biol. zhur. no.3;70-73 159. (MIRA 12-.n)
l.Uzbekski.v nauchno-issledova-ballskiy vaterinarny7 in sheep (lambs).
(Ischerichia, coli) (Vaccinea) (Sheep--Diseases and pests)

AKHMEDBABAYEVp M.Kh.; ARIFDZHANOV-- K.A.; BELOUSOV, N.A.; BELYAKOV, S.P.;
ZOTOV, V.G.; ISArEVA, Z.D.; MAKHKJDOV, I.A.; ISHCHENKO, F.S.;
KRASILINIKOV, Ya.A.; NIKOLISKIY, I.P.; NETSETSKIY, A.M.; -
PERGAT9 Y.F.; PAVLOVSICAYA, M.D.; SAMSONOV, L.S,; POLIZHAIEV,
A.I.; SMIRNOV, F.Te,$* SABININ, M.N.; SHUTYAYEV, N.A.; CHIZHIK,
V.I.; XARPENKO, P.M.; IMROV, A.I.
Mikhail Alskeandrovich Nenetakii; obituary. Veterinariia 37
no.10394 0 160. (KRA 15:4)
. (Nonotakii, Mikhail Aleksandro*ich, 18W-1960)

'QdFIIZjl~E': CIVI T .1
Discovary o- Critfl'.-idiL h-.;-ilor.- (0,;.a-rall, i~13) in the tick
ilyalomm- n. anatcherm (1--och, 'Zool. 2,lalr. 40 no. 1:2C-
24 Ja 161. (iarh 14:2)
1. ir-titute cf 'Vaterirary, Lzbek of,
Sciences, Tas;ikent.
(Tashkent Province-Protozop-) (P&xa.,dtes--T--'-cks)

ARIFDZHANDV, K.A.,kand.veterinarynykh nauk
Problem of typifying thevirus of foot-and-mouth disease.
Trudy Uz.nauch.-issl.inst.vet. 14*3-=5 961..- (KM 164)
(Foot-and-mouth diee'ase-Y

AR~M ~ZHAXQV,-X.k.,-kand.veterinarny.kh nauk
Types of the foot-and-mouth disease virus in Uzbekistan., TV*
Uz.naucb.-issl.inst.vet. 34t7-8 161. (K~A 16:21'
(Uzbekistan-Foot-and moutkopease)

LI, P.N.;,AR1FPZ4A1fqV, K.A. - ,
Ne-thoda and spects for,the control of Hemosporidia infection
of cattle In U bekletan. Trudy Uzonauoh.-issloinst.vet.
14t125-134 161. (Uzbeki'stan-Hemosporidia) (MMA 16t2)
Mbekistan-Cattle-Diseases and pests)

ARIFDZHANOV, K.A., otv. red.
(Materials of the Scientific Industrial Conference on the
Problems of Helminthology] Materialy Nauchn6-proizvodstven-
noi konforentaii po problomam gollmintologii. Samarknnd,
Nauchno-isal. veterinzu-nyi in-t, 1963. 153 P.
(MIRA 17:7)

ARIFDZHMOV. K.A., kand.voterin.nauk; BOKOV, V.F., mladshiy nauchnyy sotrudnik
Azidine against piroplasmosis and Francaiella infection in cattle.
,Veterinariia 40 no.7tl9-20 Jl 163. (KRA 16:8)
1. Uzbekskiy nauchno-issledovateltskiy veterinarnyy institut.
(Azidins) (Piroplasmosis) (Cattle-Diseases and pests)

LEBEDEV, P.T.; USOVICH, A.T.; CREPUROV, prof.; KALICHENKO, N.M.,
aspirant; MATUSEVICH, V.Fo, doktor veterin. nauk; STENIKO~ A.S.x
mladshiy nauciuVy sotrudnik; LAXHMYI'KINA, A.Nc, aspirant;
GRISHCHMOY N.F., ORLOV, A.I., veLari.narnyy vraeh (Arkhangell-
Fikaya obl,); PROSTYAKOV, A,F,, kand,, blolog, naluk; ROVYNDIKOV,
M.S., kand. veterin. nauk; AEP2-~WQII,A.A., kand. veterin. nauk
Veterinary experiments. Veterinar'lia 41 no-41-101-111 Ap 164,
(KIRA 17-.8)
1. Sibirskiy nauchnc-isal.edovatellskdy veterinarnyy institut
(for Lebedev, Usovich). 1. Poltavskiy seliskokhozyaystvennyy
institut (for Chepurov, Kallchenko). 3. Ukrainskiy nauchno-
issledovatellskiy institut zemledeliya (for Matusevich, Stenlko,
Lakhmytkina). 4. Ch8rnigovskaya oblastnaya veterinarnaya 3Abcra-
toriya (for Grishchenko). 5. Ukrainskly nauctinc--issledovatell-
skiy institut Gksperlmeentallnoy veterinarli (for Prostyakov,
Fortushnyyj Kovyndikov). 6. Uzbekskly nauchno-issledovatellskiy
veterinarnyy inst-itut (for ArIf&hanov).

ARIFDZHAN K.A.,.kand. veter. nauk
Chemical prevention of piroplasmosis and Frangaielia
infection using azidin. Veterinariia 41 no.11:42-"
N 164. (MIRA 18:11)
1. Uzbekskiv nauchno-issledovatellskly veterinarnyy
institut.

kard vt~, Ler, nauk~ TACT-~-"PD R rind. ve zt -,, nr-!jk;
J, TF 'Y 1 1,
1 .Kb. nA u:~hny-r ;s dr, k, J ~T.- Vi'
aotrudnlk
Biochemical changes In blood in piroplasmosis the effect
of azidin. Ve-te-rinarlia 41 no.10:37-39 0 t6~)*-
(MIM 18:211
1. tJzb&kski-y muchno-Igsledovatellskly veterirarnyy ins-111-1i;ultl.

IDRAGIMOV, Z.S.; ARIFDZHANOV, M.Kh.; AKTWDGV, P.U.
Prospects ror finding oil and gas in the rocks of the Upper
J'LL-assic carbonate formation of Shargun and adjacent regions.
Uzb. geol. zhur. 9 no.3:20-24 165. (I,1IRA 18:8)
1. institut geologii i razvedki neftyawjkh i gazovykh metorozhdeniy
Gosudarstvennogo geologicb-eskogo komiteta SSSR.

ARIFMHMOVI M. Kh.; DEMIDOVA.. M. 1.
Relationship beUr"n sulfur and bitwmm in the sediments of the
Upper -Turaaaic carbonate"'formtion in the southwestern spurs of
the Giasar Range. Usb. geol. zhur. 6 no.5117-,25 162.
(MIM 15:10)
1. Inotitut geologii i rasrabotki neftyWkh i gazovykh sesto-
rozhdeniy AN Usbekskoy SSR.
(Gisoar Range--Sulfur) (Giooar Hange-Bitumen)

ARIFDZHAN(YV, M.Kh.
Bitumen content and distribution in the Upper Jurassic carbonate
formation of the southwestern spurs of the Gisuar Range. Uzb.
geol.zhur. 6 no.l:,49-56 162. (MIRA 15:4)
1. Institut geologii i razrabotki neftyanykh i gazovykh mestorozhdeniy
AN UzSSR.
(Gissar Range-Bitilm n--Geology)

I AUYDZHANOV, M.Kh.; AKHMOV,, F.U.
Some data.on the fractUring of the rooks 6f the UpW Jurassic
carbonate formation in7the Gaurdak uplift. Uzb. gool. nbEr. 7
no.6t83-90 163. (MIRA -17:8)
1. Institut geologii i razrabotki neftyanykh i gazovykh
mestorozhdeniy AN UzSSR.

BAYMUKHAMEDOV, Kh.N.1 ZMROVj T.Z.; A,4_IMHANQV .T.Xh,; MWANOV, A.S.
Geology and conditions governing the distribution of
minera3ization of some gold-ore deposits in Uzbekistan.
Uzb. geol. zhur. 7 no.3111-18 163. (KIRA 16:11)
1. Tashkentskiy politekhnicheskiy institut.

ARIFHODZIG, S.
How to harmonize contractual relations between the railroad trans-
protation enterprise and other railroad enterprises. p. 125.
ZELENICE. Vol. 11, No. 4, April, 1955. Belgrad.
SOURCE: East European Accessions List, (EF-U,) Library of Congress,
Vol. 4, No. 12, Dec. 1955.

ARIFHGDZIC, S.
ARIFHODZIC, S. Premiums as a result of reduced costs. p. 419.
Vol. 11, No. 12, Dec. 1955
ZELUNICE
TEGHX0LCGY
Beograd, tugoslavia
go: East European Accessions, Vol. 5, May 1956

ARIFHODZIC,S.
Reporting the work on and the costs of railroad rails. p. 16.
kZelezaice. Vol. 13, no. 1, Jan. 1957, Yugoslavia)
~'~ Vol. 6, no. 7p July 1957, Uncl.
SO: Monthly List of East European Accessions (EEAL) L P
f

ARIFKRANOV, K.T.
Dynamics of growth and seasonal accretion in the representatives of
the genus Robinia L. during juvenile years. Uzb.biol.zhur.
no.6:7-16 161. (MM 15:2)
1. Botanicheskiy saaAN izWR.
. (Locust (Tree))

ARIFKHANOV, U. Kh. Cand Teoh Soi -- (dies) "Stu&j of the prooess of isolation
of fibers from soaked basts of gambo hemp." Mos, 19513. 12 pp (tun of Higher
Eduoation USSR. Moe Textile Inst), 100 oopies M, 44-57, 100)
-15-

ARIYMNOV, U-Kh&
. Efficiency of moving parts of the TMM-200-K machine. Sborenauchn-
isel. rab. TTI no.4:85-91 157. (MIRA 11:9)
(Textile machinery) (Bast)

ARipmNOV, U.Kh.
Investigating the process of separating soaked bast fibers derived
from hemp@ Sbor, nauch.-Isol. rab. TT1 no.4:92-100 157. (MIRA 11:9)
(Textile machinery) (Bast)

MARKOV, Valentin Vasillyevich; SUSLOV., Nikolsy Nikolayevich; TRIFONOV,
Vadim Georgiyevich; ANDREYEV,, V.V., retsenzent; ARIF%WQY,
U.Kh t O~ A.A., retsenzent; DERRUM, S.I*F
ret
-refienzent; SHUSHM f A.A., retsenzent; MJ=EV, V.S... nauchm
_1vtol, DUKHOVNYY.. F.N.., red.; SIIAMKOVAp T.A.,j tekhn. red.
[Primary processing of bast fibers) Pervic hnaia obrabotk&-,IoW
biarqkh volokon. Moskva, Gos. izd-vo "Rostekhizdats" 1961.
463 P. -(MIRA 15:4)
(Textile fibers) (Textile machinery)

OD
I'UTHORSS, Arifkhanov.'U..R,, Makarov
Shamov, V. P.
TITLE: Production of FramentfUnder the Action of 100-Mev Protons
83718
S/056160/038/004/011/048
Bolq,~B070
M. M., Perfilov, N. A.
PERIODICAL- Zhurnal eksperimentallnoy i teoreticheakoy fiziki, 1960,
Vol. 38, No. 4P PP- 1115-1122
TEXT: The authors have investigated the fragment production of the
nuclei of a photoemulsion. The emulsion used was of type TI-9 N)
(P-9 (Ch)), which allowed the observation of the charged products of
nuclear fragmentations, and a visual study of the multiply charged
particles with Z >, 3, of pL-partioles, or protons. The experiments were
carried out at the synchrocyclotron of the Mal (joint-Institute of
Nuclear Research). Fig. I shows the experimentally observed fragment
production cross section as function of the photon energies for heavy
and light nuclei. Fig. 2 shows the reduced probability for the departure
of fragments from a heavy nucleus as a function of the number of prongs
of EL star. In the fragmentation of Ag and Br, the following fragments
Card 1/2

ALEKSEM, N.V..; LRI v-.qGR.; VLASOV, N.A.; DAVYLOV, V.V.;
. SAMOYLOV, L.N.' -N':
Neutron polarization in the reactions T(p, nj'He 3 and D(d. n)He3.
Zhur. eksp. i teor. fiz. 45 no.5.1416-i424 11 163. (MIRA 17:1) "

:iACCESSION NRs AP4043612 8/0056/64/047/002/0433/0438
1AUTHORS: Alekseyev, N. V.; Arifkbanov, U. R.; Vlasov, N. A.1
Davy*dov, V. - V.; Samoylov,
3
TITLE: Polarization of neutrons in the reaction T(d, n)He
';SOURCE: Zh. eksper. i teor. fiz., v. 47, no. :2, 1964, 433-438
TOPIC TAGS: neutron reaction, polarization, deuteron scattering,
tritium, alpha particle reaction
3
ABSTRACT: This is a continuation of earl:ier research with He (ZhETF..
v. 45, 1416, 1963) and is aimed at attaining polarized neutrons of
)higher energy than in the past. The energies of the incident deu--
terons ranged from 9 to 19 MeV and analysis wa;3 by means of scatter-
ing from a gaseous helium acintillator connect-ad for a coincidence
circuit with two neutron counters. To exclude the effects of geo-
metrical asymmetry, the neutron spin was turned through 900 in the.,
~C7a7rd 1/5

ACCESSION NRt AP4043612 7
longitudinal magnetic field of a solenoid, with the reversal of the -I.:.
scattering direction from left to right and vice versa being pro-
duced by reversing the direction of the current in the solenoid.
4
The polarization of the neutrons in the reaction T(d, n)He at a
laboratory angle close to 300 exceeds 50% over a wide range of deu~-
teron energies, so that strongly polarized neutrons with energy up
to 40 MeV can be produced by this reaction. Resonance effects pre-
viously observed upon variation of the cross section of the reactionC
TO, n)He in the ground and 20-MeV excited states, as well as in
dT scattering, were also observed in.the present results. The
se
resonance effects must be taken into account in the phase shift
analysis of the q-n scattering, and are connected with the excited
states,of the He5 nucleus (16.7 and 20 MeV), "The authors are
grateful to S. P. Kalinin and N. 1. Venikov for interest-in the work
and for ensuring operation of ~he cyclotron, and also V. A. Kovtun
-!and V. A.-Stepanenko for preparing the tritium targets." Orig. art.
ihass 4 figures and I table.
Car 2/5.

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NR: AP4043612
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ACCUSICH NRs AP40436 12 ENCLIDSURS 101
SWVM7 data cn neutrcn polarizaticn
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labclec

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APOESSIM NRI AP4043612
1P1
T- HO
ad
41$"
-i m -1v
Nmtron polarization in different nuclear reO
eard- 5/5

E.'fr(M)/EV1A(h) AFWL-/SSD/ESD(t)
ACCESSION NR: AP4044581 S/0053A4/083/004/0741/0752
AUTHOR: AlekLeyei~,_N. V., Ari v, U. R., Vlasov, N. A.;
Davy*dov, V. V., Samqy1oV
TITLE; Sources of polarized fast neutrons.
SOURCE% Uspekhi fizicheskikh nauk, v. 83, no. 4, 1964, 741-752
TOPIC TAGS: neutron polarization, deuteron bombardment, proton
bon-bardment, neutron counter, nucleon scattering
ABSTRACT: This is a state-of-the-art review devoted primarily to
sources of fast polarized neutrons (FPN) of medium enercry Oup to
35 M ev) The histor
.1 of F?N research and some oE the probli-ms t-I)at
its ai' are LrLefly reviewed. Aionq with men-
tioniny various methods for polarization measurements ard
rheir _--i lv_ant ages and disadvantaqes, the ali"hors !iescrlho #*~-~e n-
used for this purpose at the Institut atomnoy energii im.
1/5

77-
MCLOSMt ol
neutrcn-(=t:w
2
3 - cyclotrm beam
4 - target (T)
5 - helim acatterer
Diagram of setup for the Measuremmt of
fast-neutrcn polarizaticn
Card 4/6,

NRI' AP4044581
uloftf
Wir 11,14

40'

INCIMMM,
Card 5/5
02

L 2738-66- EWT(m)/T/EWA(m)-2
1i P. 4334 'UR/0367/65/002/002/d~'39/10242'
ACCESSION AP502
1
AUTHOR: Arifkhanov, U. R.; Vlasov, N D4nL4py_t V. V.; SgM_G_Y1Qv&_L. M.
1 zation in na-scattErAng at neutron energies of 25, 28 an d 34 Mev
TITLE Po ari
]SOUKE: Yadernaya fizika, v. 21 no. 2, 1965, 239-242
n
TOPIC.TAGS: eutron scattering,:nuclear scattering, alpha particle proton scat-
tering neutron polarization, proton polarization
ADSTRACTi Th,e asymmetry of na-scatteri -45 to 1500 is measured for,the'
n g, for case of
'neutrons ~with. eneizgies of 25 1.25, 27.8 0.9 and 34 0.75 Hev. The-neutrons
were. Produced in the T (d, n) W-reaction at-an angle of .300 with deutron energies;
'of 9.1 A 1.3, .12.0 f 1.0 and 19.0 1 0.8 14ev. The results are compared with the
jangulaw relationship of polarization in pa-scattering, interpolated to the same
proton energies from the available data for other energies (21.9, 28.8 and-40 Mev)';~
,:Satisfactory agreement is foundbetween the angular relationships of asymmetry In
no- and pa-scattering, and both relationsbips-show identical divergence from the
Predictions of Phase analysis extrapolated from the energy region below 20 Mev.
The polarization in na-scattering Is roughly estimated on the basis of agreement
i
lCard 1/2