SCIENTIFIC ABSTRACT HUDLICKY, M. - HUHULEA, I.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R000518310002-1
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: January 3, 2017
• Document Release Date: July 27, 2000
• Sequence Number: 2
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

is
0-0 a 4_0 0- or-@ 0
a 9 is it a u m t3 is v a 0
00-1
00 9
SON
so a
*083
008
god
so 4
43
4
sew
0011
4-A-eW.-SIM-7
b=" a bit at woo we
As
A p
tallmd 14 vow'.. a
13.11 -! 6 - . .
wm~mmw m.
'0646 p tv Uw
b u
All;
00 0 0 0 0 00 0 0 *a it
0
STAS 0
/0 -so
'00
-00
.00
do 0. "*o
T;;". -00
milfilcr"54 ~(iu
Frcneb).-2- .00
pa (a g.) w" h -Ated wm
thm"ift yMdl al.fdaly.
'
6m.
0176
1
dr 1 see
.
.
. a
.
WOMWE.); pb-ylh,djatm. see
UWW*"-IA"fc"* Ow
WO WAbM 0% MY-

'
4
: ago
Tim
ed Mor.. ICHO'~MW;
4 - "0o
k# 6740, ptumn M 8. In.
Ac 3 bm Was Oh-
4110 0
i
AW10
9w
.
.
; sma
.
mass a. U4, (hvm
=

s*
in 14anmyfbkyda.
bay" ashydrWk
-
T. so*
M
I-r (davemps.).
&
me &dv. of IV, is. 1084*
ago
M. 0. Webb see
200

0*0
0 DIV. woo

OAA I I IV 0 0 v 1 9 v 0 A 6 9 1
99909996490090
1
k
)

A-
A
00 A calorimsetric maysis of O*m. Itsm". lead kl%&"-
011111 0. Wichterle and M. HadtickY (10d. fcchtt-
=-bu nt. Data a ZMA). - CWkdim Ceffill"Adw-
Owns. comma 2. del-Tt (ISITI(im resuck).-The
'"' 1 1160ra
d Cl an k1jojWm to Imm jetessely bi- 11
jjx(a) NO is Converted to alt U&WkW
Old"Inse ;j;1n., bmaliff. SOOMW to.
all rZiMic(Th" -mhr4Wcr**mm%m*(P#
al'No". I-CItIme-1
oblairifinw,11 ykIdtMoaffill.cycfamlineemerominor
00 .1 jU) in jjmk) cv. I&1 and 878 a. C1 CA 0' 1 bv- 1119d 04-111
09 4 dwo. W the blue MY Wert Lit 46' d" *0 bill ONA4
#1& 1.1131, I-Chloro-I-nitrumoucli4zais A. wessi.
I*kw !bP train CI and a wAst. of eyd"90t""*
99 (IV). will g. H.N011-11PSO's, !5j- NO mid IM 9- IW
tewo 41M. the bles yer b-,,
iv.-tew-, '(OlAent decimme.). 40 0 -
MW 6z
imatedum(V).FtOMO(fir-- &MIS . JW billion 0'
1-td. with W-32 I. Cl. - 4 111bit- Of ay"" MW & skuPy
rMbtr liquar', the latter, WON lw "WNW w-b- dv-
"Napd. slowly lit 3ul old was used for ON pip - I- a' I
r vidliss. Of 4
and U1 In abiLlYsIA. Ogh*" we dirtat*4 b
firw 4foc'mul V tusk Yon. laws. 601"Otsurift 110404sub-
with on Mg. solvent 10 give 8 biest ca'ar'
Sequent V%tn. so MIS Octal d 4 "b'* 91
S"( 'or We"": The sillIds] MW 13.7
fl,14011-IfOAc (8-2,ji IINO
N.OAc In UJIM cc. If we tressted with Y, e1c., 90
-0`01
&Is St.& MOV&LLW"KAL LifINAIIAN CLAWKATIVis

I
,
m s 0
U
.
a 6 1
I s i
.

I he Wor color - Test (or UtNOI I: n1m twaille (neistr"sell
with N&OAc 9 isiddle) 6 treated with IV and wvv-rAl drops 00
V and the blue color said. with sylene. Dem c4 U:
0.01-OJA c. in 10 cc. HOAc in a "mated tube, 03-0.3
cv. V, And 30 cc. HA) we dild. to M m. wkk HOAc. -00
The extimilea N then mrsimml in a Lamp walvermil
reWrwlrr; a rrd filter tSudsm 511 red) gives Vfttcf

vislums, nw tirrvisisto ill 0.1w, 40.011) "IAw sulm.
Is -2%. The tallaclinst of ;Y usirar iv -intUwly drid.
O
i
)
f
1
1
i
4DAc.,s Dem. of cy-r1ofirtanum - 3 cc. 0.3 11
n '
j,
1
)
Ij. OAc added to a %Amldr cents. 41.01-41M g.
ketow. now. afterw min..21 cc. HoAc, 0.5 cc. V. and HgO
toW cc
vol
td
h
l
"
i
. age lu
.
tl
e ex,
; t
j
m 6 nicesured a%
with ff. fj*J4. of IjjX()II: 0 Ill 41AM S. NIW In I w,
Irv 0
11.2 11 N&OAr. 0. 1 tv, cyriolwit4mutc, UP1 CV. IIOAc and
11
25
t
V
Fk;
.
m.
a" dil
. toAfllv~ Willi IIAl . I stin of
..
hrImphilimilk- arid (VI): DAI AILS g. 111%,011-110 In .1
'
'V. Ii'(). ne"I'sliAge'l wilb;l "i
NAMI lit 141 11),hrreal"I
24 lain with 2 m. mAt M VS.* slier ~Mn. 4 m4-1.41vr. V
and dan: to lkpm.. the rKinic6m i4 uwxtuml. I.W.O.

------ -
wool

U 0 10 Mli is 4 it a -4 j i k i k ij& a Igims lowl; a stirmeme 7 9 IF
0 0 0 : 0 : 0 010 0 *1* 0 0 0 40 0 0 * 9 0 a 0 0 Is a too*

009
a be
On
0
0
0
0
j*4
go
00
00
.00
cleUne's
NjI,C1cd(itbik
(A
at.
$two .7 I)tfgw
peg
tape - 64
I-M - Juv. , IW7*'. 80
lso"IM661 01-1 Va.
we,
jarIM16% VC.
0v dc rribit.dry ..
c Compd. in wto dwo
ztd. 4 tiff"
out. tb
to &JACO the Ill b"PS I
.5, ~ ~ Ill, ~~j
I
111pnoa goo
re ultosh
SO P11
IA
MICLU,
to 1.
*g 12W %. %Nbtl
irrin t a to .
with 14 tw 40.10
to a clear
10- the t=;;;
Ad dlkd With
mist d
v! - Wine to
1. 7 Lwd:j Nits I
is it tbe W
0611 b--- d
cratfuurd after bcr~woc
lar-1 of t 161
04 live 65,
(W,;-Jy~pow
Vol 10
JAAA"O
A**
*I ----
SIVII Ito A
With IC011' INA (IV)
1
S
rals. 10' it'll 3
to pg~atxfw) P",dGb"-`a ube
slaw. 40 j It Is blot 190* tbo t I WS.
CA- 103 (15 S. ;,va tuto at b"tod
;~~* . be coalcols
aw to I "
CC. obs. On
to ;xAcd ic stisid- If bo
%be a , W, M
&*-nods-sho.-
tive VOW -
'-% I with 6
Ibcc
bet AWN. to
941, =11.3 I It o"a jttcd
;Iwb It.
It .14,01 . _ j,h 1()D CC -
'9 to US- 5 tboo t c-) V N
woo 46 vclOzca 0,70, 69,4 ;2jda.
6
41i q I tb 3 9.
tb* t1w gailt. ~'*d todW- *1 - 51 . 10i
off Mil CCt, tubelint CO'.8 1.51105. (().7 6.),
As. 00 C.11.6%, ;,a t a t ,
0 'J1(`I`_1',;,Wd3ob9I-- ~1*15ct-
030ce. 954 do: orratf, to- .1 4 tim"
jw- nal. mathre-At 11-O'se
b and tb
.bit and ANOW
11,16,isat o4q-a*dyl'VbsgDcc- Cjts*,jIebAtVu
J~~ to 2 dryuc?,a on i N, I . of %J'Awb
latit. to .wit 10-01 of us.
I fict I" Uou"d.
Zoo,
- DIU tm ratt k , ,0r#&
- - a
Sad6d
ia r I"Wir oollr "a' to
w6d% 64 am tafel", d6o Sm a OW-4. wd6 Stv" the dis"..
Is foe od!nl ssuo :: "" V P-5..
he WOO I VL in Awd. to or c"ItMINA. 4A 10 %. 4 CO-
tww to WW 100 - t ljter a ;mcd. 11VA I redoction 13:~ 6- - ;
tA* Or to a
tb (VI) ba . ),.*M.
the 1;;ows. ocu is can ofavi ii ~,1109'er
NgsW1e 6$& -" 12.49. did 1~Vjj5jujtj,. T.U( .5 a.
ight the t -pbi ad the 221-2% 182*-
Over* -lk' 0 0 - ..I
!;- IM4
I
With ter
Camp red, filua_ to Its`_"O'Wrb;;; o"i" .1 wo g. at to
19
cc.
No
.6 Is.
to cao-5.4. 71.1,
bu,.t
*W,
)61tcf
to& is% I
ad b0 34M
bS. 140~ exiow. :A-dmd~sro
bs
viva V ivu) I ..Ji&
9411ho
341- IR:-C~Y 110
to
T ZA a 3,
d
-00
.00
.00
geo
zoo
0*0
goo
too
000
goo
4* 0
goo
goo
woo
zo 0
co 0
Ago

%baktf 4(k) g. at 2.6~j Nq-H# mad the Wit. astd. after 7
I I
his. lk time, an d min then Is obtained the J414

'b
T
IN4 '
dr
ir
sil
ok
W) ;;~W of VU
le
2W7

0
a
ris
. w.
.
oo
o,
.
y
; j
The Draduct fivem the Clemmemom roductiam of YU gives
the um oition (wised ts
) as that from the moollows
p
roe mother Hqwjr Itu", lix- (ly-1 D 4 Vill lpt" w Ito k.
so
.
.
redwalm of ". VU rrdwW wkb Adum tialmlyst OW H U09-19-1
HOAc is gamiwi Ift.3 Im. by 2.9"~ 0, al the -It
2W cc
i
-midthoproduct ystd two t I.C.H4 whit. OM
-a &w -
i.11,NMOWO is. M A
F .
n
2W cc./he., the 11OAc diOd. AT. and ball of the llill~
%A
*bite
3
2
iddin
I
i
h

0
m. 23
. prow. by hastfig - .
m
r.. y
t
s
p
I*W "Wue txsikJ u
as-
ll
%A
"'to 411% tai=
C
00
1
11m
dr Wkk
d
Vj ThOllb and Na at
:d3l
M -
o
p4
,
C 11 N(k m
"y"b, , t , - , - .3 -, a - (dtcmpa - I - DAY.
1~ -
v
t *0
00 smixt.
,91 a
0
o
-
y dWd. Nj -
.
hea;4j .1 =6
10.5 Ion., vmW to 00-70'. eutd. with ::j:, U by twiling in a both at 3W* with St Own
~
-h'
i
1100 at 2
4110 cc
I
S
1
~ so
00 CJl The CAa asi. washed with 140, the mAms some
'
= .
n
j
. 1
X.)
produc
j
At
0). After
4 6
uivs
1~
0
J4 r
lo
x1 9411
d
by
.. .d the r.M. diKd. t. give 13 It. of the JF-
dW -d&q of VU. N 95-d'; Okra&. tom. 237*. To (I S.) .
.
o
,
.
q
emauniped 1,76 ce.14
j
tittering on the ),I ao~. nor filiorAiv is cmtd. and acididird 00
In HOAC adds 7.8 cc. 2 S Rr ado. is HOAc, while Har IS with 6.6 8. "Mcd. 110; clymn. givre an Utow"fifabir
0 treated
11
10
i
2
H
60
liberated: . to 6 cc. mid cooWW #in I
'
MIT
Su" a
i
N
h
14
VU
h
d
O cc.
n
(U.
9 K.)
1
pCoduct" M. 2m)-V.
with 6 drops 3Vi P-hyd". -0 the milt. r~Apd. 40 a 00

o O
t
VANS
e 4
rm o
wr
p, of
, M.
s
.
(
Ch (1.5-2%) is Vowed 60 hes. hato to S. Vu fm Ito ot.
I HOAc at the rate a# iW-M coc
look do mM 11.0 bath Old CTy%ld- IFOM CJII SiM J-4`CrY'-4-S-j'-
I-exule, on. 10"'. 00
s A him. to C!, p the wwml& .
.
the 4CM dbW. of is a bidY410, m- Z34-4-0 CLrctxv T. Masm 0
04o mum andthe (16X.) cv"d.bVa4dWgJkOH- 06
-6 71- a- 1-1 so
OO
W
t
W J
0411
so F----
.
.
O
- 90
00
0
0

04
*0
a
00 00

of cyclipliammittimmis Ollim'. ld".Iiwduckl
and J. IlAr #Ttcll. Univ.. Itirsam) , C.Wks"'" Cs"ka
I&W. ckgm. Cummams. 14, MI-JIMMUM" 11118611).
c take "xime (11 way lx- it"ity alkylited to gi
whk,b int cwwim kmids a( ter
01106, Stable lis U)"A UkUM at taillps. lu 40**. st NIOD' I
#at= -dPwAleld-it. It win Pirevil. tW viddims 11 mk&.
d"pi smillati, to ZM g. I In ajoil ii. hiiii " N&(M. bftt.
inl on a almn both 0.6 hr.. camilisgi irsig. with Stso.
waslitims the tit. wisb %aH�(h will MO. dry* om
NaoW),. and disig. U litregal. in thla way wem: Me
ViM). thg MI-1.5', h,l dl- 0.9477, *6 1,4N11
1.4111W. 1.47,310. and 1.4-,W-, J.v the C, I). F. aad a
linft. ft-P.. And Fj (V .5,; ). 1"S 111) 1'. 11's 04'. N. "Ill.
it'- OX'73, a' 1.0043.1.411OV. 1.471M. mid 1.47003 for
Theallylethirr(II11.1h,
1.1817"Wittlifirtid.t" time.
yield by ulding 2441 a. I in.4it Act. %.4n. ut 104 C. X011 141
211) 9. Cll,;CllCll,llF, hi-AtMg Oil A SIC4111 tMlh With OC-
clskinAl With 110I.Clig. with
iltying llw CS1, .'m I.. AIM '11,11g. If (I 1.4tt lit a
WAS AddCli 10 Ill'; 14CS3118 t~'. IUF14 lit fill.) with
latlow 4dl*. ont~ijghth of the mAn. ficAttif to 101' (4 viuk
itaction mcurred), the pnxlssct himitol to 121)". and thel
fest Of thr Illixt. Added shrioily; after the feActiun W sulp-
*ided. the nsi%t. w3i tmnstnt twito itc. licutrAliml with
(Njj,jtC(N. And CAM With J~tj(f. &~AjlffJlJC-
I., lit, its. CA, (ftAit K m Cola t mi-d frmn i hr c %I,
V. UL Flint

KNOA),-A favid, simple Owlyak of (hell lent CY61-
b-awww (0-cyclohnaW (0)-YhOli (11)21 &Mulatto
to 1-2%. iff hUM up= Cbe mensurrawat of the a atwi I
Cd tW MMWk; the COMPO. at the samPle- 6 read directly
IMM the trkafskr disgram constructed from messurc.
mitts. Thedalzaregivrnfor
mizu. whkb OM(Mift it" than 201Y0 In. (rum Is to NO,
U. and 211-100% 1. P. V Elam

mid Needle #m
ilk. bpdrWpk 411 A&COM
g. CKh Im 1470 W.H We
yfrI&d I'A It. (=%) J4
ykm woo nbtakwd
It. crol in 0 0. MtCO Wki
~'Aft -01084. ftheresm.yj
6jmkJ W crolem"Isydr-lib
w1mm L 04%hommeftak
Debmal md Miles Hudlkkt
1.). Chtm~Wd~-M. 45"
JD (VIA 6 ) walwd by
6. WWA Z;91;4 161th IOU
1064wkellbm.; otbeream.
WO-24mimd (U), Us 41V-4 1 '.
, caMislog 10A It. I with 14.7
I of. 1(80 CNIS. 27 ff. 11,406
kd 3.7 Us a yvlkmrm
all,
War
an k1011H. 11 ipwv
Lm-&eW=emrcAnmk wid). t".
kAlly Wilk ft. cCl Clio
,~, M), 1 1, i
asidLwd In MtKO-with Chromic- mill. at ef env# X A a,
4%) felf"Or "f, M. 79", obt4lowd by ether fit".
Id. Hgdlkkt,

li
C A
. -- j4 1404 _
" -0
W's 1, fop j,,N-Wwb
4r. P. 4
go" M
as 5"k,j-,kloj . wla*"
. ,Ay 4A.
I, ~:~c orri-lovoll

'IV % - / 0
/(~ ft4 e, ,, - -
11 I~f
A
,olljoind-g- -vj~0w*WMWI~wPwbbrW PW-WO-
V,:Wlklill$ jy 46. M74UI
S JF~r ow 93
on= 771114mckt

C~-, cb

.. HUDLICKY, 14110S
"Methody preparativni orgaul.cke chemie. fvyd.11. Praha, Statni nakl. technicke
literat" 19560 Cmethods; of preparatory reactions in orFanic chemistry. lst
ed. index3: It
p-381 (Praha, Czechoslavakia)
Monthly Index of East Furopean Accession (EEAI) LC, Vol. 7,, No. 6, August 1958

ry.,11PIV. R ow aLL VC.R., mztvgair~ v;L~qUig wuh -
tip.-

Synthesis of
Of
If
#wmuu
LI ull. 5o, 771KIK.
01

dzechoslovakia/Organic Chemistry - Synthetic Organic Chemistry, E-2
Abst Journal: Referat Zhur - Khimiya, No 1, 1957, 900
Author: Lukes, R., Hudlicky, M., and Janu, Z.
W&
Institution: None
Title: Reactions of 1,3-dichloro-2-butene. H. Synthesis of 2,3,4-tri-
methylpyridine
Original
Periodical: Chem. liety, 1956, Vol 50, No 2, 258-263 (Published in Czech); Sb.
chekhosl. khim. rabot, 1956, Vol 21, No 1, 140-145 (published in
English with a Russian sumary,
Abstract: The action of benzylamine (I) on 1,3-dichloro-2-butene (II) yields
bis-(*r-chlorocrotyl)-benzylamine (III). Treatment,of the latter With
concentrated S04 leads to the evolution of HCl and the formation of
N-benzyl-3-aceNyl-4-meth,yl-1,2,5,6-tetrabydropyridine (IV). Distilla-
tion of IV at ordinary pressures causes decomposition with the forma-
tion of 2,3,4-trimethylpyridine (V) and toluene; distillation of the
hydrochloride of IV likewise yiel" VP with the additional formation
Card 1/3

Czechoslovakia/Organic Chemistry - Synthetic Organic Chewisti7j* B-2
Abet Journal: Referat Zhur - Khimiya, No 1, 1957, 900
Abstract: of benzylchloride. Similar cleavages followed by rearrangement have
been described previously (V. Prelog et al, Helv. chins acta) 1942,
1654). To one mole of I in 360 ml of water with 3 mole!) of NaOu
add 2 moles of 11 (20 minutes at 420); raise the temperature to 980
for 3-5 hours and stir 4.5 hours. At that temperature III is obtained
in yields of 67%, bp 123-5-133-50/1.2-1-7 MMj the picrate, mp 132-1330
(from alcohol), is also formed. Add dropwise 0.5 moles of III to 150
MI. of 96% %S04 at 800, heat while passing a stream of air through the
solution (to remove RCJ) for 6 hours, pour over ice, make the solution
alkaline, and remove COO IV is recovered as the picrate in yields of
29.5%, mp 146-146.20 (from alcohol). IV is obtained from the picrate,
bp 1310/0.2 mm, n&0 .1-5519, d~O 1.0492, M, 69.82. Distillation of IV
at 115-4000 gives V in d 20
1-5151 n22.7 1.5138, drOeOl.,,840f 34%, bP 188.5-189-50/740 mm, rT)
, D ! 3 (nD markedly decreases during pro-
longed contact of V with air because of the high hygroscopicity of V;
this explains the divergences in the physical constants given in the
literature). V is obtained in 47-6% yields by the distillation of IV
witn 3% HC1 (gas) and in 65 .2% yields from the distillation of the
hydrochloride of IV; in the latter case the picrate is also formed,
Card 2/3
%,tlru 11.3

AM~LUeaddsunldes. M.Ildlktt_C..h-l7.126,
Sept. la. lVb7.--?Welbphen;n-e-u-xWWTT-g) was nd,ei with
8 g. CFjCOjH (1) at -150 and t;je mixt. heated to go*.
An exothermic reaction took pkwe. The mixt. was heated
2 hrs. and I tvapd. in secuo. -11ve residue gave (!!! crptn.
from 20 tal. HtOOM l.amunilide, at. 112-130. similArly.
benzanilidc (at. ld2-3*).f brazoplmoone oxime and *-
caprolactust (bes IOD-1 rmua G4-8*) from clahexanone
oxwe were obtained. T. Mim-,

C I< C) S
CZECHOSLOVPMA/Organic Chemistry - Synthetic Organic Chemistry. G-2
Abs Jour : Ref Zhur - Xhimiya., No 8., 1958P 25059
Author : Hudlicky Milos
Inst
Title : Reactions of 1.3-Dichloro-2-Butene. IV. Reaction with
Grignard Reagents.
Orig Pub : Chem. listy., 1957.- 51.. No 2., 336-34o; Sb. chekhosle khim.
rabot, 195T, 22, No 2. 577-582
Abstract : 1.,3-dichloro-butene-2 (I) reacts with RMgX -through the C1
atom in allylic position, to form chlorolefins
I z
RCIUCHICUCH (TI) LrR C,,Hq (a)., n44Hj, (b), CdH5-(c)
and C~HSCH,Xtld) ; 3:Ia-c yield with concLirated H.,SO-t.
methyl ketons R(CHAXPOCH3 (III)P while Ild - a mixture
of methyl naphthalene and methyl tetraline Boiling of
ether solution of AW (from 1 mole Mg arA 1 mole RX)
with I mole I gives II (RX., reaction duration in hours,
yield of TI BP in OC/ma, nD (temperature In OC):
Card 1/2

C7,ECHOSLovAK3:A/Or~Dzic Chant try - Synthetic Organic Chemistry) G-2
Abs Jour Ref Zhur - Xhimiyap No 8j, 1958.- 25059
C HrERP 3 13, 83.92/50., 1.4434 (18); c&H,,,Br.. 6p 17..
;1-5-97/lt.5 tsolution of RMgX added to boiling I;
IIb contains admixture of n-C*Hag) C6H ) 605,9-19p
102-105/151 1-5332 (20g; C&HXH.~Cl. 2.. fr, .9-12,/
14-5,, 1-5261F (20)- d 1.0259. 0.08-0.16 mole of II
p
stirred at 25"with k;_100 ml 96% H-SOV., bloving a
current of air t;hrougi the mixture) to get III (Rp dura-
tion of reaction in hours, yield in %): a, 18.72; b,
3p 38; ap le5s 53o
Commication III see R71MiM) 1957, 6oh66.
Card 2/2

Pb D r, i (- (,-, Y~ /,-/,
.CZECHOSLOVAKEA/Orgenic Chemistry. Synthetic Organic Chemistry. G-2
Abs Jour: Rererat Zbur-KhLidya, No 4, 1958, 11247
Author : Hudlickyp M.
Inst J-
T'Itle The Beckmann Rearrmpment in Trifluoroacetio Acid
Orig Pub:~Chem- ListY,, 51 -473 (1957) (in Czech)
No 3, 47o
Abstract: It has been established that CP COOR (I) is both a catalyst
and a solvent for the Beckmann garrangement of acetopbenone
03time (II), benzopbenme oxime (ni), and cyclobexanate
oxime (IV) and of the corresponding amides. For a concen-
tration. of IV in I of 39.5% at teneratures of 75, 87-5,
and 990 the follovIng values have been obtained for the
reaction rate constant: 0.00067, 0.0035, and 0.14; tor a
concentration of 2D.21j: 0.0051, 0.013, and 0.036; for a
coucentration of 11.0~: 0.012, 0.025, and 0.18. The re-
Card 1/2

CZECHOMOVAKEA/Owganic Chemistry. Synthetic Organic Chemistry. G-2
Abs Jour: Referat Zhur-Khimiya, No 4, 1956, 3-19.~WF
action appears to be first order and the velocity decreases
with 1-0n-reariDg concentration, II is dirsolved in m8lten
1, rz-C-'--=Pd P. hrG, yield Z acetanilide, mp 112-113 (80%.
of the I is recovered). By a similar pi-ocedure III yields
88% benzail-'lide, mp 162-1630. E -caprolactam by lOo-1010/
2.5 mm, mp 64-680 is obtained by a similar procedure from
IV in yields of 62.51,.
Card 2/2

~~rl IYN
CZECHOSIDVAKIA/Organic Chemistry. Synthetic Organic Chemistry. G-2
Abs Jour: Ber. Zhur.-Khimlyap No Up 19561 36284.
Author : Jarkovsky Pesata, Hudlicky M.
Inst :Not given.
Title :Reactions in the Anhydrous HF. III. Synthesis of
Dichlorodifuorometbane.
Orig Pub: Chem. listy, 1957, 51, No 4, 625-632.
Abstract: Synthesis of CC1kFjrrom ccl~ and EF was investigated.
Small quantities of SOZ and water do not hinder this
reaction. Catkaytic activity of SbCI,,rrspIdly de-
creases in the presence of CSZ which reduces it to SbClj-
As the result of that, when using technical grade CC14,
small asiount of Clit should be added, It is recommended
to employ 0.08 mols of catalyst for I mol of =~, 10-2Yp
excess HP, and maintenance of temperature at 100-120 DC.
Card - 1/2
azEcHosLovAK:rA/Organic chemistrY- SYnthetic Organic Chem'strY- G;2
Abs Jour: Ref. Zhur--EhimiYa, No 11) 1958, 36284.
A test run conducted (that involved preparation of 6.25
moll; of product) extended far approx. 16 hours. During
its course were used 150 gr. SbCIX, 1020 9r- CCI and
300 gr- anhydrous HP., The reactants were ~:=6
brought up to 100-120 C as pressure was raised up to 30
atmospheres (1-2 hours)- The gaseous products were cOn-
densed. Yield of CCI.~FZ was 930 and of CC1jF Was 2%-
For part II refer to Chem. IlItY, 1952, 460 92.
Card 21 P2 1,7

CZECHOSLOVAKIA/Organic Chemistry. Synthetic Organic Chemistry. G-2
Abs Jour: Ref Zhur-Khim., No 13, 1958, 43446.
amounts of catalyst increase the formation of Mi.
Under the above stated rditions there are formea
3-1~ of CHM~F, BP 9-10 -
V. Preparation of C.4CljFz (I) in the usual equipment
(see preceding co=mnicalion) is difficult due to
insolubility of CIC14 in HP. The reaction can be ef-
fected by increas ng the amount of SbC13-, which acts
as a solvent (0.56 mole per 1 mole C4C1,,)- .7 The op-
timum ratio HF:C4C14 is 4, temperature 150', pres-
sure 2D atmospheres, duration 16-25 hours. Yield of
84.W/6, together with 4.4% C'Zqlj~_ and 2-ef, C'C1jFA-
Card 2/2

acid!' '111d
51.
I
Ph! it' if~A I

('11 12 111 CC!
mi', 11 it 11 1... I 1 .1 1 t.4
it

inwill!I14. "lid 1'. 0 --i

_j
Ali". JJCJ (1. 1), t1it t J)'_j I'l); 11) I'Ll V,
4 idtfate. extil . with C41 N, Ow i1q. I-) a Akoh!, d l61" N,L011
- vot, with cllcl~' ('1111 thc ('110, ext. disid. to give 193 g.
.
-Ir cc 1, bj .6 -0,102, iOn" .". 98-0
(i., ICIA ;,!III the ~Ar.

JIMIEtti WidL . Ai UNd 44~Z
AU(
ikox! (II)i tt;v 1394 4:1,
Oh~ K.
I '. - 1,11, .. IF "a) 11.1 Ij I e, so
=VL;
thfut.-Ch it,
14C TAW"t ott kc, licutralilhir: with NQOI-.'. wv9-

K--1vu r,
n',"
by ('i R. 111) with 3A X. 111.11 by
ritiltring itr ILI ild. UtOll, 4 stil. IfC), 4viii :1 int. 111"i, NaUlf 31)
-----------

ti rK. at rv-,m tnfl eAtr_ %%it h itill an it C~114 yicltliji~ 7
fil PA, (dil. utoll).
NaOill by tb- wilal 1"I.
i.tij. III, W. A-,d 11,1_1
uf the WPIlCu4t t-rOml haviug W-W,
ix tabt. (9 70 g. U1, 16) -iod. S, i'na FA) S. nopbAint
in-) .14 gllAi w-M 6 fle-atEd 3 firs. tc)
ibin.-:4 t:miti,no I-lied I lirs. kith ZIO n-A. .50 'C'
INW, the cjq f
53 g.
M.sc. a, 135" tilt co~'ILA mxtioll wINI alLilized,
bl;~ky M71terird ~ff. tli~ Cll!rAt, with
CIICI,, ';w aq. IQ ;,It
5, ~ , 10. to dryn, ih~ ~--in
.iln ~ ji. tud , 'I't ~Illi C.11" z
voi'-c ,-I TV- - . -I- 1~ 1
ilq~ 1, AN, 'ViLl., NMI, Lli~ R'll. nak-rcl. ana ivyT~-
ov~:f ptch xavt ~-('4q,Ipeffityl)vakric arid. 111. 177' ~EtOll-

k/
CZECHOSLOVAKIA/Organic Chemistry. Synthetic Organic G
Chemistry.
Abs Jour: Ref Zhur-Ehimiya.. No 22, 1958, 74110-
Author A. Posta, M. Hudlic)~-
Inst 'p -
Title Reactions in Anhydrous Hydrogen Fluoride. IV.
Preparation of Difluorochloromethane.
Orig Pub: Collect. Czechosl. chem. com=s, 1958, 23, No 3)
535-537, 537-539-
Abstract: See RZhMm, 1958, 43446.
Card 1/1
~Y,
.0
Co.
S-
s-.3 8 i
sk
o atn A 4`3 .9 t 11
4-2 9
J,N JAI a
17
V
C C
43
4 d
P..~
n la Z!l aNds."
0
Its d.
z:1
0 A
d,
age,

i,
..Ti
I MICKY, M. ; MARES, F.
"Reactions of 1.3-dichloro-2-butene" V, Preparation of some pyridyl substi-
tuted fatty acids. In English. p. 46.
COLI-ECTIGN OF CZECHOSLOVAK CILMICAL CGOqJHICATICIS, Praha, Czechoslovakia,
Vol. 24, No. 1, Jan. 1959.
Monthly List of East Europsan Accessions (ESAW, LC, '701. 8, No. 6, Sert. 59
Unclassified

06620
AUTHOR: - Hi-d 1 4 czzcH/8-53-i-i6/20
TITLE: Conference on th6 Chemistry of Fluorine
PERIODICAL: Chemicke listy, 1959% Vol 53, Nr 1. pp 51 52
ABSTRACT: A conference on the chemistry of fluorine took place in
Rague during June, 1958, at which thirty papers were
presented. They were parly reviews and partly original
reports. Original work has been or will be published
in the following journals: Collection, Chemicki PAMYll,
Cheiaicke" zventi and other journals.
(n.b. A report on the conference in given in this
journa.1 and the reviews will be published in its further
issues.)
The Czechoslovak Chemical Society, Czechoslovak AceSc.,
arranged on June 9 and 109 1958, a national conference
on the chemistry of fluorine* The aim of the conference
was to make publically available information on the
present state, nationally and internationally, of the
chemistry of fluorine, as well as to evaluate the results
obtained in Czechoslovakia in this field aud coordinate
Cardl/7

06620
Conference on the Chemistry of Fluorine CZECH/8-53-i-16/20
work in individual centres and to give new incentives
for research and technology.
The conference began in the large lecture theatre of
the Faculty of Chemical Technology (Technical University),
Prague. It was opened by the introductory remarks of
Academician Lukel and the conference programme was divided
into four sections.
The first half-day session was devoted to lectures on tlie
basic raw materials for fluorine chemistry. The lecture
of J. Kalpar (Faculty of Lhemical Technology, Prague)
contained concrete information on the occurrence of
fluorite. The lectures of Z. Dobial( and J. Spurni
(Faculty of Chemical Technology, Prague) and of J. KocoureR
(Institute of Ore Research, Prague) reported on the
preparation of fluoritle ores by flotation. A lecture
by M. Odehenal (Faculty of Natural Sciences, Masaryk
University, Brno) dealt with the winning of fluorosilicates
during the production of citrophosphate.
The second half-day session was made up of lectures in
Card2/7 the field of inorganic chemistry.

066?0
CZECIV8-53-1-16/2o
Conference on the Chemistry of Fluorine
J. Suchard (Corporation for Chemical and Metallurgical
Production, dsti nad Labem) revieved work performed uy
the Corporation in the production of hydrogen fluoride,
cryolite, fluorosilicate and inorganic fluoride; his
lecture was supplemented by detailed information on the
production of hydrofluorle acid (S. Vondrug, the
Corporation); chemically pure fluorides (V. Tyl, the
Corporation) and fluorosillcates (J. Dubi-kar, the
Corporation).
K. MatiaAfovsk:f (Slovak Academy of Sciences, Bratislava)
delivered a very detailed lecture on the production of
elemental fluorine and the difficulties involved.
V. MachaVek (Institute of Nuclear Physics, Czechoslovak
Ac.Sc., Prague) presented a paper on the proparation
of uranium fluorides.
Two further lectures dealt with health questions.
J. Marhold (Institute for Organic Synthesis Research,
Pardubice-Ryb1tv1) drew attention to the dangers of
Cax-d3/7

06620
CZECH/8-53-i-16/20
Conference on the Chemi try of Fluorine
tjInstitutq for Sj? tiluical Researflv,Prague)
fluorine and : compounds and 99 c a/spoke on no--
significance of fluorine in dental medicine.
The analytical section was inaugurated by the review
given by J. Vrettal (Antonfu ZApotock-j Military Tecbnolo-
gical Acadomy,.Brno) on the analytical determination of
inorganic fluorides. Reports on original work dealt with
the determination of water in high percentage hydrogen
fluoride (K. Otto, M. Uhl~r-, Institute for Resear6h in Macro-
molecular Chemistry, Brno); pyroanalytlc estimation of
fluorine (K. Zubec, the Association), spectrographic
determination of fluorine in silicates (A.- Spatkovi -
Stodolovd, Central Geological Institute, Prague) and the
determination of fluorides in the atmosphere during the
welding of basic electrodes (L. Hanslian, Regional Station
for Hygiene and Spidemklogy, Olomouc).
Methods for the analytical determination of fluorine in
organic materials were summarised in the review given by
K. Otto (Institute for Research in Macromolecular Chemistry,
Brno).
Card4/7 The work of J. HorfiSk and J. Kbrbl (Czechoslovak Ac.Sc.

06620
Conference on the Chemistry of Fluorine CZECH/8-53-1-16/20
and Institute for Pharmaceutical and Biochemical Research,
Prague) dealt with the determination of carbon and hydrogen
in organic compounds containing fluorine. The subject dealt
with in the work of J. JanAk and J. Novidc (Laboratory for
Gas Analysis, Czechoslovak Ac.Sc., Brno) and of V Pokorny
(Institute for'Research in Macromolecular Chemistry, Brno)
was the chromatographic analysis of gaseous organo-fluorine
derivatives.
The fourth half-day programme, the richest one, was occupied
by papers on organo-fluorine compounds.
M. Hudlicky' (now of the Faculty of Chemical Technology,
Technical University, Prague) spoke on the mode of intro-
duction of fluorine into organic compounds, on the prepara-
tion of the main types of organofluorine derivatives and
on the applications of fluorinated compounds.
The subject of V.%7Aeinbhlls (Institute for Research in
Macromolecular Chemistry, Brno) paper concerned the
technological methods of production of the most important
refrigerants (freons) and their application.
Card5/7

06620
Conference on the Chemistry of FluorinOC'ECH/8-53-i-16/20
The lectures of J. ZdraA1 (Institute of Research In
Macromolocular Chemistry, Brno) and of H. Lamar and R. Rado
(Institute for Cable and Insulator Rose rc~, Bratislava)
considered the preparation and properti:s of fluorinated
polymers (Seflon, teflex and copolymers). '~
The paper of-M. Huillick-y (Faculty of Chemicil Technology,
Technical University, Prague) dealt with the use of fluorcs-
derivatives an media for and catalysts',in various organic
reactions.
D. Ambros and J. Rovner (Institute for Research in Macro-
molecular Chemistry, Brno) presented a communication
dealing with the auto-oxidation of-trifluorochloroothylone,
the crystallisation of its polymers and the determination
of its molecular weight.
It in egtinated that 70-80 chemists participated in
the conference, among whom was a celebrated guest,
Professor A.L. Henne, the discoverer of freon, from Ohio
State University, USA.
Card6/7 The conferenceshowed that the chemistry of fluorine, a

06620
Conference on the Chemistry of Fluorine czecH/8-53-i-16/20
not very ancient field of study, is being fostered In
quite a number ofOrwh laboratories and a number of modest
but valuable results have been produced, as evidenced by
the number of papers published in Czechoslovak chemical
journals (see the bibliography on pp 52-53). It is
necessary to support to the utmost the development of this
branch of studies so thatth4Vmay eventually be able to
reduce the 10-25-year lead which the advanced industrial
states have.
Card7/7
HUDLICKY, M.
"Fluorine compounds as catalysts and reagents in chemical reactions"
Chexicke Listy. Praha, Czechoslovakia. Vol. 53, no. 3, mar 1959
Monthly list of East European Accessions MAIL LC9 Vol. 81 No. 71 July 59, Unclas

HUDLTCKY, M.
"Organic fluorine compounds"
Chemicke Idsty. Praha, Czechoslovakia. Vol. 53, no. 3, Mar 1959
Monthly list of FAst bwopean Accessions (EEAT), LCp Vol, 8, No. 7j July 59, Unclas

HUMIC,KY, M.
Organic compounds of fluorine* I. Fluorinated acetylenic carbinals.
Coll Cz Chan 25 no.4:11"-1209 Ap 160. (EUI 9j12)
1. Research Institute for Pharmacy and Biochemistry Prague.
(Fliorine) (organic compounds) (Acetyl group)
(Alcohols)

MASS I BOOK MWITATIC11 S07/5889
Hudlicky Milos
Khimiya. organichaskikh soyedinaniy ftora (The Chemistry of Organic Fluorine
Compounds) Moscow, Gookbinisda , 1961. 372 p. Errata slip inserted.
6500 copies printed.
Translated from the Czech by lu. 1. Vaynshteyn.
Ed. (Title page) t A. P. Sergeyev; Tech. 9d4 V. F. Zazul I okays
PURPOSE: This book is intended for orgodo chemists and for workers in the
plastics industry and in establishments which produce or utilize refrigetints.
COVERAGE: The textbook is a comprehensive,,treatise on the chemistry of organic
fluorine compounds, The b4isic'inforadtion necessary for experimental work
and laboratorY*t*chniques..,vhich are in MW oases unusualp are included,
and the possibility of further development of the chemistry of organic
fluorine compounds is discussed. Special interest in shown in fluorine
Card 1/4
The Chemistry of Organic Fluorine Compounds SOV/5889
compounds which oontain a considerable number of fluorine atom in the
molecule (polyfluoro and perfluoro derivatives, or polymers). These com-
pounds are characterized by inertness and thermal and chemical stability,
and are of theoretical interest because their behavior differ.3 from that
of other halogen compounds. This ampliiais is reinforced by the rather
extensive formula and subject indices and'the chapters on propertiess
-taxicityp and applications of fluorine compounds. The authorp who stud-
ied the chemistry of organic compounds at 014o and Purdue Universities
under a LINESCOgrantp thanks persons in the U, S. who have assisted him.
He further thai6i--s bin wifep-.A. HudlickW, R. Lukash and'Vikhterlat
Academicianaj, and Raynoyll, Engineer.
TABLE OF CCNTENTSt [Abridged3:
From the Author
Ch. 1. Introduction 13
Card 2,/,4

The ChwAttry of Organic Fluorine Compounds SOV/5ag
Referencea
Forwda Index
Subject Index
AVARABLEt Library of Congress
SUBJECTs Chemical Engineering
Card 4/4
318
3"
359
EN/dk/pp
2-27-62
HUDLICKIJ M.
%thods of organic chemistry. Vol. 4s Halogen compoundsw by Bouben
and Wayl. Reviewed by M. Hudlicky, Coll Cz Cbem 26 no.7tl899-1900
J1 161.
(Houben, Jose) (Wayl) (Chemistry, Organic)
(Halogen compounds)

HUDLICKY, M.
Organic compounds of fluorine. Part 3. Reaction of trifluoromethylalk.71
ketones with acetylent. Coll Cz Chem 26 no.12:3140-3146 D 161.
1. Research Institute for Pharmacy and Biochemistry, Prague.
KAKA6, B; HUDLI(XI, M.
Czechoslovakia
I
liesearch Institute for Pharmacy -md Biochemistry
Prague - (for all)
Praf,rLeq Collection of Czechoslovak Chemical Communi-
catiorwy-MO-M, 3:962, pp 2616-261T-
"Quantitative Deteraination of Fluothme and its
Isomer by Means of Infrared Spectrophotomet3-j.11

EIDDLICKY Mllov
1-7~~
Improved apparatus for hydrogen bromide preparatione Chem listy 56
no.3.2:1"2-1"4 D 162,
1. V79kmny ustay pro farmacii a bioohemliq Praha.

KAKAC, B.; HUDLICKY,M
Organic compounds of fluorine. Pt.7. Coll Cz Chem 30 no.3s
745-751 Mr 165.
1, Research Instituts of Pharmacy and Biochemistry, Prague.
Submitted February 25, 1964.
----------
RMIN WN
fiVl
L 650-2.1-62
Acussion NH: AP5. 02.3335- cz/dbo8/64/0OO/7Oi2
H hi 4
Hudlickyt.-I.1-.6
aA_,v fluorinA
-in the chedUdt -of --o,,~9_af%tC--c0ffi?0u
TITLE: Progress
MURCE; Ghemicke listY, no* 12, 19614, 1373-1395
ToPIC yAGS.- fluorinated organic compound, fluorination, chemical engineering
_--pro.P tax", last 6 yeari is reviewed.
_(1030rl 0 ~-and- I+.
---Fl:uor imU,0n__agZn_t5 PVO d ne~bho-da o- ill-rou'loing
i~_~ii-wr-&Uo7eovvoun -a w-wval-u~-4-A ~,tiozns-or---_organ-io-
comr.10unds are d.isou3sod'-~iido-iii-nat~6d--orga.--i6::a-K,3n'
ice]. processes used in their determination- are :revi_o_wdd-.- Usea--
of organio fluorine compoundi are dencribad, and individual---
:'plaatia materials based-on those are discus3,3d. Thu present-day

L 6501.1-65
CGESSION NR. AP5023335
production of or'ganie F oampowids in Czechoslovakia is revi~'wado
7he main uses at present are w3 refrigerating rlix.Lda; trifluoro-,
eth-,lone i--i manufactured and p3lymcrized into a plactic trade-
nan;e, "ToPlexttj and a F basad aarootic named "Narkotan" in alao
i produoade \9
Orig. art. has: 49 formulas, I graph,,
AS OCIATION: VyzkunW ustav., x.-O farmacii a IiInchemii, Prague (institute
Pharrwcolog7 and Biochemtstry)rir,
SUB CODE: OC, W
sny-rr=D. 00 - EXI.
su,
NR RrF SOV- 006 CTRER! 11? JPRS
Card '~~2

CZWfi03LOTAXIA
HUDLICE(o Vi KAXao B
fOP rASIUWq and BloobadetVYo
prag" - (for both)
akmmL-
*Orgsudgi GONVOIN" Of flu*vimo Paru 100 ft" 87stb"IS
of 6 n%Gp"Wjg%*jjW# S -bydroxImlodamo allopole-
objdV4mWl"U*QlMo and 3-uotb44pftUMo
ftaiwch lmtltat* ror iumay mA 31 o*hfv-'J'.,wtryo
Pmf" - (ter both)
Pro # 98.1) WIN at 9wam"Snk -al Oda& 20MULO
ilaVW49&6# xhlbolVIF,
kw-vt gs Tt!&%

0, Duane
CO-lAtryl I.CGOI.Vis
A-Mrdf D-CIAO!2I met IlTan
A:fLU.tt*,,t 1-11tuta at 2.1-s@
*wvia 11421eh'
17
03t&: 3 Properties of Doolvibsualleld
A.14 Isolated rres Salmonella Typhimurimm Irradiated b7 UT ud
Adjo.,
co-autharal--l.,
tment-a,941adiabLowwo lw%LVA* of
rishl.
81910, Nuts M., Department of Redlebtelely, lactItuts it Pwlftr
Teringes IsorLs IWISKI,
UNA111,Noss I., Department of ladlableloo, Inatituts of ftoloor
rsliWsos 'torts Wrloh'.

HUDNIY,-PLEVNIK, Tamn a; SIMIC, Marta Ma
Quantitative changes in the base composition of DRA
(desoxyribomeleic acid) extracted from Salmonella Typhimurium
irradiated with ultraviolet rays. Bul Inst Nacl 11%231-233
161.
1. Institute of Nuclear*Sciences "Boris Kidrich.0 Department
of Radiobiology, Vinea.
or

BEGAR&TIC.. A ; HMIK-
GLIBLyt V.; JANKOVAG, J.; KAMM, D.;
510-9 -
.. -/ Aur-Too C--
I
Labeling nuoloic acids with lootopeoand their use. Prim. radloaktiv.
ixotop'. 2 no.3M-8~ D 161.
.(DNA) (PHOSPHORUS ISOTOPES).

HUDNI&Pigm , T9-; KMZIRp D.
Structural changes in desoxyribonucleinic acid after UV
irradiation in Salmonella typhimurium. Bul sc Youg 7
no.1/2:34 F-Ap IQ.
1. Institu, 1B. Kidricp* Vincal, Beograd.

H MO LIN, Vlad W r; vionja
CompUcations fol.3owing suboccipital Welogram performed with lodised
oil. Srpski arb. calok. Isk. 90 no.1323-29 Ja 162.
1. Hourolosko-psihijatrijaki odjel Opos balnics wDr Mladena Stojanovicap
u Zagrebu Sef: dr Vladimir Hudolin.
(SPINAL CORD radiog) (IODIZED OILS toxicol)
(BRAIN die)
-5

HUDOLIM, Vl.; PZMVCIC, F.
Diagnosis of tuberous sclerosis; two personal cage reports#
Nouropsthijatrija 4 n0-3-4:209-217 1956.
1. Is Neurolosko-psibijatrijokog odjela (prodatojalk prof* dr.
J. Breitenfeld) 1, PAntgenskog'zavoda, (predstojalk prof. dr.
S. KiLdrnks) Opos bolnice Dr. MI. Stojanovica u Zagrebu.
(TUBIMUS SCLIMOSIS, diag.
(Ser))

Dr.; HUHIK-SIMM, J.; BRIMMMM, a., 4r.
Psychiatry and clinical psychology, Lljoeo vjes. 76,116.11-122
513-m518 Nov-Doe 56. j
1. 1z-Neurolovk1-p~1ch1jatr1j~og 9djola Opes boluice dr.
M. Stojanevica u Zagrebu.
(PSYCHIATRY,
relation to clin. psychol. Oor))
(PSTCWLOGT
relation to MehipW of clin. peyehol. Oor))

" mir
_ MLIN, Vla&--
Retinal changes in tubeA-us- -sc'TW?Mft;--Keuropaihijatrija 8 no.1/2:
30-42 160.
1. Iz Neuralosko-psihijatriskog odjela Opce bolnice dra X.Stojanovica
N
u Zabiregu (Sof odjelat Dr.Vladimir Hudolini
(TUBEROUS SCLIMSIS diag)
(PJ=A die)

VZOLIN, Vl; RIESSNER, D.; KADRUKA, S. I XWEVIC, M.
Giant osteova of the lamina cribrosa. (Contribution to the diagnosis
if frontal lobe syndrome). Nouroptibljatrija 8 no.4:306-316 160.
1. Is Opee boinics dra M. Stojanovica u Zagrebu: Neurolosko-psihi atrijaki
odjel (Soft Dr. V1. Hudolin) Kiruraki odjel (Sef: Dr. D. Riessneri
Zavod s& radiologiju (Sef: Dr. S. Kadrnka) Zavod sa patologiju (Sef:
Dr. M. Knesevio).
(Os7EcMA oase reports) (FRONTAL BONS neopl)

- HUDOLIN, Yladimir, Dr.
- ------- --
Prevention of alcoholism, therapy and rehabilitation of alcoholics.
Lijec vjes 82 noe6:473-W3 160.
1. 1z Neuroloako-psibijatrijokog odjela Opce bolnice "Dra M*Stojanovicaw
u Zagre rALCOHOIJSM prey & control)
. -4. , , . ..

BUDOLIN, VI.; PRAZIC, B.; MACIVIC, V.; BARAC, B.
Social problems in traneveoOtiom. Nouropol.hijatrija 9 no.1:54-U
161o
1. Is Neurelooko-psihiAtrijakog adjelA Opce bolnice 'Dr. M. Stojanovica".
Zagreb (Sef: Dr. Vladimir,Hudnlin).
(SEE DXMTION)

HDOLIN Vladimir dr,
Prevention of alooholizu, therapy and rehabilitation of aloohoucs
(according to pneumencepbalographie examination of 147 cases).
Med. glasn. 15 no.2/2at76-80 F 161.
1. Neurolooko-psihijatrijaki odjel Bolnios "Dr. M. Stojanovical u
Zagrebu. (Sef odJelal dr Vladimir Hudolin).
.1 . (ALCOHOLISM) (VENTRICULOGRAPHf)

HUNLIW,,yJadA~4!~1 HUDOLIN,, Vianja
Comp1jeations foll(rwivg suboaciPital WelOgrOm performed vith iodized
oil. Srpski arb. calok. Isk. 90 no.1123-29 Ja 162.
1. Neurolasko-palhijatrijaki oA$al Opes b6lnics 'Dr Mladena. Stojanovica*
u Zagrebu Soft dr VUdiair Hddolin.-
(SPINAL CORD radlog) (IODIZED OILS toxicol)
(BRAIN die)

HUDOMIL, Josoof
10 years' experience with dacryocystorhinostomV. Szomesset 97
L1003:141-149 S 160.
1. A Budapostl Orvostudommvi Baotou IL at. Szomklinikajanak
kozlemnyo (Igasgato: lonay Tibor eastoul tanar, at orvostud6immyok
kandidatusa)
(LACRIMAL APPARATUS surg.)

HUDOMM, Jozaef
On foreign bodies at the chamber angle. Szemesset 98 no.2:82.4%
A 161.
1. A Budaposti Orvootudoz=yi Bottom II oz. SmemkIinikajanak koslomanys
(Igasgatot Nonay Tibor egyatemi tanarp as orvantudomwqok kandidatu3a)
(WE foreign bodies)

PT,'DOMEL, Joz.99f; TOTH, Margit
Considerations on the Groenblad-Strandborg syndrome. Szemeszet 99
no.2tln-3.18 A 162.
(PSUEDOXANTIIOMA MASTICUM)

-HUDOMEL
Abnormal course of a retinal vessel in the central fovea. Szemeozet.
99 no.3tI66-169 S '62.
1. A Budapesti Orvostudomajiyi Egnitem II. oz. Szomklinikajanak
kozlemenyo. (Igaagatoi Nonay Tibor egyetemi tanar, as orvoltudmanyok
kandidatUsa). (RMNA bLlood oupFay)

ACC NRI AFtt) SOURCE CODE: cz/0017/66/055/004/0203/02191
0195
A
AUTHOR: Huducekp Zdenko (Fngineer) 1
ORG: none
TITIE: Opening time in mine networks with a non-grounded neutral point with regard
to contact voltage
SOURCE: Elektrotechnicky obzor, v- 55, no. 4, 1966, 203-210
TOPIC TAGS: electric capacitor) electric resiatance
ABSTRACT: On tho'basis ok an energy criterion the
article derives the limiting opening time of a low-voltage not-'.
work with a non-grounded neutr"l point upon contact with a
'human bo(?y. 7be limiting time is reduced to a funobion of four
;variables: the network voltage, the total leakage resistance of.
the network,, the partial capacitances to ground, and the resis-
:tance of the human body. The influence of the individual vari-.
,ables on the limiting opening time also is analyzed. In con-
Iclusion, the necessary technical procautiuns a130.aro givpn for,
the distribution of the high voltage (1000-3000 V). This paper was.presented by
Engineer M. Zapletal. Orig. art. has: 10 figures and.24 formulas. [Based on
author's Eng. abst.) (JPRS: 36,8111
SUB CODE: 09 / SUBM DATE: lOOct64 / SOV REF: 001 / OTH REF: 002
LLB UDC: 621-316.1.,04-78
Lj~Lgrd 1/1 / Y / /I)-

HUDYMENKO, Fedir Sydorovych
I ~ I ~ - --, - . ~
, ,
[Higher mathematics) Vyshcha materatyka, Kyivo Vydvo
1-~vivslkoho urliv., 1964. 379 p. (MIRA 19z1)

14TZOVIC Peter inx.
YAthod of approximto deterranation of the excessive regulation
and the duration of the regulation process in linear sy3t6me.
Autmatizace 8 no.lilg-19 Ja 165.

HUEBER, Josef, inz,
"Zo~;-IrXting" by William G. Pfann. Reviewed by Josef Hueber.
Sdel. tech 3.1 n0-89319 Ag 163.
i
I
i
I
i
i

RAVLIK, Otto - HMM Ad
Results of sorological investigation of tozoplasmosis in domestio
and wild animals. Cook. spidem.mikrob. imun. 9 no.5/6:391-397 Jl 160;
1. Ustav spidemiologit a aikrobiolo it T Praze.
(TOXOPLASMOSIS reterinaryl

RUNGARY Chemical Technology. Chemical Products and H-13
Their.Applicati-;n--Ceramics. Glass.
Binding-Mateirials, Concrete
Abs Jour; Ref Zhur-Khimiyat ITO 3, 1959, 9063
Author t Huebscher, He
Inst --.-Not given'"
Title Foam Gla84 Its Pr9duction. and Use
Orig Pubs. Epitoanyag, 1958i io, No 4-5, 109-112
Abstract: The methods of producing foam glass (FG) are indi-
cated: 1) by introducing gasses into molten glass;
2) by introducing intense gas generators into
molten glass; 3) by expanding bubbles under vacuum
in the molten glass, which contains a large quan-
tity of gases kunclear glass); 1+) by mixing glass
Card 1/2

HUNCKEL, Stanislav
- - ~ -4. 1. -.-, -- ~
Development of research an soil mechanics in Poland. Review
Pol Acadeny 9 no.lt6-13 Ja-Mr 064

HUECKEL,.Stanielaw, prof. dr Inz.
A conference on soil and foundation mechanics in Budapest.
Ina i bud 21 no.8:295-296, 3 of cover Ag 164.
1. Technical University, Wansk.

HUECKEL.4 Stanislaw, prof.dr. Inz.
---~ ~Ihe "anchoring Ci-P20ity of rigid horizontal elements awsk in sandy
soil. Archiw fWdrotech 7 no-3s297-314 160. (EUI 10:2)
1. Katedra Fundamentowania Politachniki Gdanskiej, Gdansk-Wrzsazcz
(Sand) (soils) (M.1ding)

tislawq prof
A brief review of the scientific research in the field of marLie and
harbor tMiraulics in Polandq Vodoprivroda Jug 2 ncl-7/8:119-123 '59-
(Elul 1091)
1. Ecole Polytechniquo do Gdansk (Pologne)p ot V-directour do .
1'Institut Hydrotoohnique do l'Academis Polonase des Sciences, Gdansk
(Poland_-Harbors) (Hydraulics) (Ships)

MECKEL, Stanin2aw
%ginearls hydrolog7ll by G. Ramenierts. 4vieved by S. Hueekel.
Archiv hydrotech 8 no.4:623-.621+ 161,
1. Redaktor Naczelny kwarta2nika "Archivum Hydroteohniki".

HLIELLE, #i, mgr inz. (Gdansk)
Wrigerat and air-conditioning installations for vessels
f~,hing in tropical seas, Bud okretowe Warszawa 8 no. 6:
207 is 163,

--- - I - --- --- -- - -- ---- -
11UGET, Marian# mgrop (Od"ia)
-- - -- -- --m
Marine insurance. Techn goop morska 12 no.2:52 162.

HUGO, Rri
-1
"Science of plastics for engineers" by C.M.v. Meysenbug.
Reviewed by Jiri Hugo. Stroj vyr 12 no.3t238 164.

HUGOIJ.; JIRGUS,H.
Rheology of hard poly7inyl chloride. Chem prum 14 no.2t8l-86
F'64,
1. Statui Vyzkumny ustav materialy a technologle, Praha

CZECHOSLOVIJM/Chcnical Technology. Chemical Products H
n
,-nd Thoir Uses. rart IV. Synthotic
Polymers. Plastics.
Abs Jour : Rof Mir-Miniya, No 15, 1958, 52090
Author t Hugo, Jiri
Title : Epoxy Resins for Low Current Electrical
Applications.
Orig Pub : Slaboproudy obzor, 1956, 17, No 8, 447-452
Abstract : Cast epoxy compounds UPON 2100 B (1) and
UPON 2200 8 (11) wore prepared in Czocho-
slovokia. I and II are relatively low
viscosity compositions, consisting of
epoxy resins and a reactivu solvent (mono-
meric substance containing a vinyl grcup).
Card 1/4
CZECHOSLOVIXIA/Chenical Tuchnology. Chemical Products H
and Their Uses. Part IV. Synthutic
Polynors. Plastics.
Lbs Jour Rof Zhur-Khimiya) No 15, 1958, 52090
Curing of I (initial viscosity 300-500 cps)
and of I,~j (loco_18oo cps) wns accomplished
at 20-50', using 8 purcont of the curing
agent and 0,4 percent of the Xcelerator.
Thu process was distinctly exothermic* In-
troduction of i_~ filler (quartz, sand or
mica) increased th,:- specific heat, at tho
saria time docronsing heat accumulation in-
side tho cured slab. Presentod ware cheni-
cral and physical and dielectric properties
of I and II, cured at 200. Specific impact
strength of I and II was correspondingly
20 and 30 kg.'cr,,/cm2. Stitic bending yield
Card 1 2/4
132

CZECIIOSLOVIaLrq/Chomical T,:..chnology, Che-Acal Products 11
and Their Uscs, 1~,Art IV* Synthotic
Polymers, Plastics.
Abs Jour Rof Zhur-Khiniya, No 15, 1958$ 52090
strength (kg/cn2) was 420 and 620. Ultinnto
compressive strength was 490 and 710, while
ultingto tensile strength was 260 and 280
kg/cm . The nodulus of elasticity vias found
to be 20100Q nnd 389000 kg/cr,2, Brinell hard-
ness Okg/m2) vias approximately -16 for both
rosins while Martens heat resistance was
520 an& 570 and Vick's heat resistance was
709 and 780. Diolectic strength of the re-
,jins was 17.2 and 18.2 KV/m (200), while
surface rusistanco was 3.7 x 1012 and 4.2
x 1012 ohms, ruid 2el x 1011 and 4 x 1011 ohms
after water irziorsion for 24 hours, I and II
Card 3 3/4
CZEGHOSLOVIXIji/Cho.nical TocImulogy. Chomicna -,rLjucts H
vnd Their Uses. Tart IV. Synthetic
IL-lastics.
rolynors. '
Abs Jour Rof Zhur-Mintyal No 15, 1958, 52090
shrink loss upon curing than opoxy-poly-
ester compounds. Cracks wore not formed
in cast I and 11 rosins upon their sub-
jection to heat cycling, between -70 to
1200. -_ L. Posin
Card 4/4
133

'Distr: 4E2c(j)
Creep Chamterlstles at poly Yale-
rialov$ Sborxik 038, 816-29(=-Div ~-.Iments'
V11yarnitles have been carried out at 10-
41X) Xg./Sq. Mr. and at O-W'. Test spechnons have heen
subjected to a const'. ten.4ile load at atru. niolAturcs of 30-
857, and at a ternp. of 21*. and the deformation mcas-
.urA as a function of thrin, Bending tests indicated bend-
ing flexures vgAable with time and permitted the detn. of the
so-called creep elasticity modulus at various temps. It was
found possible to use the E,(1) curves for the calen. of t
creep curves, O-W*. The calcd. curves wire identical
with the measured ones for stresses up to 100 kg./sq. cm.
For ambient temps. or foT lower ones, correct ions are made
/J" for moisture content.

ZILVAJI, V.; HUGOp J.
The machining of pl"tlq.,,_Jsm4*dOqO opt'5 no.11.329-331 N :6o.
1. Statni vyzku=y ustav materialu a technoloViep Praha.

HUGO) J., inz.,
I- ----- --
Mechanical propertlies of ccnstruction plastics. jerma mecli opA.-
5 no.11043-346 11 160.
1. Statni vyzkumny ustav materialu a technologie, Praha.

(RM
L 082h9 7
- _Tj-P14
AP6033024. SOURCE CODE: CZ/0032/66/016/007/0551/0558
AUTHOR: Hugoo (Ed&ee'r .1 Xrous, M. (Engineer)
JQ
ORG: State Research, Irts*ti~'te' of Materials, Prague (Statnt vyzkumny ustav
materialu) -J,
TITLE: Evaluatl`6h",o~,t I strengt of plastic materials
SOURCE:, $t~oJire:~"A*A- ---iv 16-.~ no, 7, 1966, 551-568
TOPIC TAGS: p1j"i1c,:-.1a'rininat6d plastic, polypropylene plastic, polyamide,
polyvinyl chloride, 'epqx1de, epoxy plastic, stress analysis, mechanical stress,
static test
ABSTRACT: The methodology of testing and evaluating results of research on the
strenght and behavior of plastic materials exposed to prolonged static stress is
explained, and a surv9j,'of the resul s is presented. A group of polyamides,d
polyvinyl-chlorides, polIy 19and epoxy vitreous laminateqewas tested.
propylene,
Semifinished prodticts:pr6pared.by VUGPT Gottwaldov were us .edfor the tests.
The dependencies '"d. valtie's-determined are presented in dia&Tams. The paper
f
Val
-172
C
ard

L 08249-67
kcnw, -A-f 6-0 3
was presented by
19 figures and 11 forMujgj6.,#`~'
SUB CODE: 11 f'; 90B
LCard- 22
-ofessor, Engineer, Doctor. Orig. art. has:
kqed on authors' abstract]
~.none/ ORIG REP: 010/ OTH REP: Oll/
:Ez A.
V,

"Elemontary wave meohaAico"-,by W. Hoitbf. Reviewed by P. Huhn.
Aota chimica H=g 38 no,2sl7O-l'71 163,

A-- -0 AIM-
HUHN 11. Arproximad Ivt so]"
140 , .- A ---a - 0""11 03)
dkv"x WMA ASMI(ar
xj, to oil
Wise Sarias
Md-O X-GeArxim ~A', VOL
oul
j
3 1932, NO. 12, ~- 370-379, 9 11P)
P1
The toact!" W411ico of complea chemical reactions
vm loveritigatid. Instead of almaltancously considering
all the chemical processm only the steps determining
Tocludcal Abst. the rate of the elementary reactions fpvolved - starting.
F) ITOO vi. noting, branebinl, and rupturing - reactions - wen
Iskin- into account (' four-it sp mochavism'I By this
zWbod the vroce" MAY be characterized by two dUler.
outial equations - one Mating to the conversion of the,
stating material and the other determining the rate of I
I OW cbs"a in the concentration of the active centres. It'
00 fate Constants of the alimentary reactions no known.
the explicit solution of the differential equations is P002W&
ible W approximativo numarkat Integration 9. 9. by the
zukr-cow-1 polygon Meow. If these constan- an
k. gh trials a quartet
dU%=tW equations
to.
A Vmqipyi

VTh. mcchj'~-['mn ("f
oll VrIv R I A k"' J!,
0,~Tnval dcc~vnpa Cf Ctl.'~ I
'A cl-l'
-M b e. dpjt EuZyc-At'd
stein d ~Sl), Tl:c t,t,.e :f Cl. tht
a'. (C.A. Vt. 45
ay be " I -kay-
met tht 50"ifiratical nl~ aw. to 2 .1-.
thtmortut6l reactiom CIO + 0,;;t CIO, tAff
L-c2l,) ajul C10i + C' lQj v.-! Cl-.(?. (W!

IV
--okdAllott -f-pugovil vf 0
U-
a III) I'10 I :I
.1 Iii tilOV 111,411ii'l i:, (~~r tilt.(
flu'll 111C il!Ili
the ( 1, 11
'U"T - rv-:,
Ivrivatioll (if thiq uquation it r,-Ijjt;wtAiip k gl%vil for
I v I ,.11 'it ut -
111L C~j ollatit"n 14 tilt, fit iji, )wxut ratiml "mm,
lKill-ling to 0C poillt Ly
InVilmiroWe conventration &-tla By
of -this-eqTmUnti it I~cpiiw oddcut that tilt, kwlectric
IItWitt tit unitt.-titiable fit -, ~,tltitiovt uf an alito asniplex
Ivithout the addi(imt (if uiccsak v (if
Iig;i - oll%ivali,tit III (tit, %,ikm-v I;; tiv: k-oard (,,it k
it ht 111.1 'it tho
alld the mmt.,tt- ic;i 14 tic,.V,

naillf [kill (his State. The nuthollatiell Cquati'llu-,
'am tit n
11-mon-tical um~wt-atimv, v,tre aillitiol w
I~Iria!imr' of th'.: "Ot
tomi-111triti'm of frin-4 JTt~int L~ ll~lilg kAl, Salt,
whid. tit" 1.14111,11 [kit thtir (11~1-'Ifiort I,, fmm m.t-

33. The mectlactsm Olt NORVICOcUdull
anillahlbli(on -Z. c;zab6 P Flu hn A. B
Magyar Klm'aiFM -7171 ~1.11
vdiral - 0 - pp
7 figs., 2- tabs.)
IL
tfi~--U-Udoiln and gentrAtiar-chanism of hamogenco" It
-latirmtoi by M. Pdri'71PIC.5 -of ffre
-Alift I m It Is kn(nm that a sabstance Or-
lig
lzave OPPOSIte c ects on the same, r&dtca!S del)endil
of the "actarits.
teutive, coaccutmdom
'SUbject to oKvftrdrg Iteiween the Etabilized
-- --------
radilvdartrid the starting matt,dal fit between the ptiklif-
1124L41- nUlkIdl# gkllil: ttW -VtL%thhJjjyXjj fWjjrAj%. DfffjCq
itics
Hanle" fit -041 - 1"ith(Midtl6ml fennulktion ot this
extrefticly rmt4en jm)m-,,g were Solml Palcoessfully br
tr-,Ntegp inechani-tru
ying tlv~ Infildlifel of the "(01
~tcvclojv%l by the nutharm. To tL%t the valldity of the
CqUatirms nlitallied by thearcilkal dctivatints thc nitrous
0%filt-COUlvitell o1, luldlilted dcl-cullwodtfial of pro I
stiddlyAlle %6% slindied as a functinn of the nitrous o2le,
n ntrattall.

INE
Lit, /I/ /A
HMGM/Pbysical Memistry.. Kinetics - CoMbUstioup ExplosiOns- B
TOpoAIWdst3*'. Cauvaial
Abe Jour: Yof M=-*XUmLyaj,,Wo 290 '1058j. 732".
Authhr T. Berces#2.~~
Inat
Title iOn the Eatension of the Concept or the Four Sta"
Mechanism. 1. General Considerations. 11. Application
in the Analysis of an Expe Kinetic Curve.
Orig Pub: Acts, phys. at chi&. 8zegedj 1957o 3p No 1-4s 95-W;
IM-111.
Abstract: I. The system of differential equations describing
the concentration chan of active centers (dn/dt)
and initial rAst4noes for not-brancbed ebain
reacticas., the chain carriers in which are 2 active
centers converting one into the other in succession,
Card 1/3
ROGARY/PhYfic9l Chemistry. Kinetics. Coubustion. Explosions.
Topochemistry. Cataysis.
Abs Jour: Hof Zhur-Khimiya, No 22, 1958t 73279.
van reduced (assudug that the chain were long
Zgmt)to a system of equations (RZhXhim,, 1956,
) for single center chain reactions proceeding
according to the fou stage nchadem; origination,
continuation, branching and chain rupture. Ex-
pressions of dc/dt and dutdt for the case of thermal
daeonosition, of 80,zF~,Z OOMixv 45%, 13796) Pro-
ceeding through 2 active centers f n = n I + n't 0
(C1) + (SO)Cl!J vere obtained as an exanple.
II. The system of differential equations describing
the kIDIatica of the thermal decouposition of
80 CI (see put I) was numerically integrated
varying the rate constants of elementary stages as
Card 2/3

d lnh~j
~chal*
ply, Siered, L-
tk, z P.
Hu SUM" si
tht:,stahfli~tstlon of to used In
the nwhanism of cat I ted chem.'
--math. detsils as liven wid applIvA to da"
'4h4 d-P I r On. of pt(?,*Mehyde and the dftvmpn. of H,
Induenjed b)~ M Paul. H. ltn!msm,=~

ISM
'Meanim of the Laflusocing factor of the homogeneous
chain cat& yals'jand Inhibitlom P_ Ifuhn and F. Marta
(Univ,* Siegidi Hunfl. AcAl T=svieledieni7t. Aila
Phys. e .4, 33-44(10M)(In English).-A
relation was established between the half period of conver-
sion I,/, and the Influencing factor F(I). defirittl as the ratio
of the stationary chain component of the rate of the In-
fluen"d reaction to that of the noninduen"d one. F(l)
of the thermal decompri. of propylaldehyde catalyzed b NO
was caled, from expti, b/, and I~y choosing by trW surtable
values for the characterlstlevonsts. 0. 4. as for the eQuation
F(I) - (I + 0 I)IVI -+28,1 + 6 11, where 16 the conen.
of the iniluencing substance, for tho date of StAveley and
Ifinshelwood (C.A. 30, 66311) %nd SuM, d of. (C.A. 53,
833c), and of the more tittallest work, within NO resture
0.00-M.00 mm ol'the authois The agretment Mween'
Wed. - and ex U F(JI) waxgd. The process is chain.
of of a at
mvp.tO _4Sr YJ ------ B.",

HUNGARY Physical Chemi sitry. Thermodynamics. B
Themochemistry. Equilibria. Phase
Changes. Thysico-chemical Analysia.
Abs Jour : Ref Zhur - Khimiya, No 12, 1959, No. 41548
Author : 11uhn,, P.; Beckt M.T.
Inst : ToRgiven
Title : Some Mathematical Considerations of
Successive Equilibria
Orig 'Pub : Acta_phys. et chem. Szeged, 1958, 4,
No 1 2p 45-53
Abstract : From known equilibri= constants, the
concentrations of LIT_ '.,,i~7,
I ~jd f2
OdIj_7, Od,; 7 and t/ were ca -
cula ed for mdl"ecular r"ractyona of cad-
mium iodide in a 10 -3 to 1 M solution.
Card 1/3

EUNGARY Physical Chemistry. Thermodynamics. B
Thermoohemistry, Equilibria. Phase
changes. Physioo-chemical Analysis.
Abs Jour Ref Zhur - Khimiya, No 12, 1959, No. 41548
Similar calculations were performed for
cadmium bromide, cadmim chloride and cad-
mium thiooyanate solutions. The equili-
brium constants for each stage of complex
ion formation as well as isoelectric points
of several cadmium complexes have been
calculated. A method for the calculation
of dissociation constants of pol basic
acids (based on LIUmeasurementsT has been
propojed. The concentrations of Z_H~7
2NO 9S04_2 and L112S04-7 in
16-4 to 1 M H2SO4 solutions were computed.
Card 2/3
15
HUNGARY 'hysic&l ChemistrYi Thermodynamics.
T~prm6chemj try.
ClAngag. Millbris ph... B
14Y31co"chemidill Aalyal's.
Abs JoUr Ref ZhuV , A"MIYA, No 12, 1959, No. 41548
PInally, Ion co,cent.,
tiona of oxall., tions In the sojU_
Ic acids were eat Citric and Pyrophosphor-
were pres ablished The results
ented In tabular* r,,j.
A. Zol0tarevskiy f0
Card 313

PMTODTCAIS: Vol. 64, ~Io. 7/1, -T,11,71-411ry. IIIV,
rf&7 KF'TAT FOLY-MAT
Huhn, P. Discussion about the Bodenstein method in the frane of four-stage, -.echaniam
p, 263
Vonthly list of Zast European Accessions (EEAI) Vol. 8
p 1100 2., LC,
Fdbruary 11?59., Unclass.

Dictr: 4E3b
7- --of, nundoi functiozi. M-,
to
T. fk-,k andL._Udff-(UMV cArtw.-
Maij. i. 11sixg. Z(F-.285M15D5MY..
cf)miklcx forl"alkni fu')CtWn of Djtrrum (C.A. 35. tM70),
i, was mutlifts by 11warAlfins the stability axims. of com,
plex systems like NI(SCNN. Nis, CdBro, lIsCh. Pof the'
Alucyaunte systein and Cdf, the expil. data obtained agree
with those caled. by Fwaacus (C.A.I. 47. 85M) and Leden,
(C.A.36.MH40). The ii - 1/m polsits tit) not have a definite
Chtin. R1iln1fiCAS1t%,, but the Wilts V)herei is rin hiteger ex-1
hibit a dcfbtite chens. mmung In that the conespindingi
cOmplex attains amax. value at thisvoint. R,.9.hfuntt--

HMIj Peter, a kemial tudowanyok kandidatusa (Szeged)
An account of my Moscow study trip. Ker tud kozl MTA 15 no.1:91-93
,61. (EM 10:6)
1. Szegedi Tudoetanyegystem Szervetlen es Analitikai Kemiai
Tanazeke, Szeged.
(Rusoia-Chemistryl Physical and theoretical)
(Hungarians In Russia)
(Aoadeaq of Sciences of the U.S.S.R.)

HLMTI Pete kandidatus; KALLO, Danes, kandidatus
11-~L=TJL
An accont of the work of the Working Comitteo on Catalysis
in 1963. Ken tud kosl MrA 22 no.lslO3-104 164.

UMMOT-P ing-1 OMMU.- I-P 149.1 NITUJV.o ing.
Gcnsideratio~m'on the oboice of the optinmm tensim utili-
gkition for aleotria drives In thO oil extraotim Industry,
Strol ei gaze 14 no.9t448-456 -8163,