SCIENTIFIC ABSTRACT HARDI, I. - HARDY, G.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R000617910010-6
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: September 21, 2001
• Sequence Number: 10
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

HARDI, IBtvan, dr.
MdmffAr-, -
Istvan Hollos, 1872-1957. Ideg. szemle 10 no.2:64 May 57.
(OBITUARIES
Hollos, Istvan (FAm))

HARDI, Istvan, Dr.
.. I - "; . '-w -1 .
Place and significance of psychotherapy in medical practice. Orv.
hetil. 99 no.23:778-782 8 June 58.
1. A Janos Korhaz Rendelaintezet (igazgato: Baknes Tibor dr.)
Idegosztalyanak (foorvos: Gereb Tibor dr.) kozlemenys.
(PSYCHOTEEWY
place & a ignif icance in nied. practice (Ifun))

HARDI, I., dr.
The use of frenolon in ambulant psychiatric practice. Ther. hung. 9
no.3/4:21-24 161.
1. Pest County Council, Psyrhiatric Centre (Head: Dr. I. Hardi),
Budapest.
(TRANQUILIZING AGE:fS) (PERPHENAZINE)

HARDI, Istvan, dr.
Observations on the psychology of nursing. Maj,7 pozichol
szemle 18 no.1:53-60 1619
1. Pestmegyei Tanace Idegbeteggondosoja vezetoje.

HARDI, Istvan, dr.
"Handbook on the science of neuroses and psycho-therapyn by V.E.
:Frankl, V.E.Geboattel and J.H.Schultz. Vol.13 "General science of
-neuroses and general psychotherapylp Vol.4t Special psychotherapy
II. and prophylaxis of neuroses." Reviewed by Istvan Hardi. Magy
pasichol szemle 18 no.2t240-244 161.

I t. van
su;df V-.-
-k -, Given Narzs
Country: Hungary
Academic Degrees: Dr
Affiliations [not givenj
Source: Budapest, Magyar Fszichologiai Szemle, Vol XVIIIj, No 2, 1961, pp 244-246
Data: Review of "Handbook of Neuroses and Psychotherapy. Volvmes I and IV," by
V. E. Frankl, V. E. Gebsettel, and J. H. Schultz. Muuich-Berlin, 1959.

RA dr.; PAJZS, Zsuzennna, dr.
Therapy of depressive conditions with levomepromqzine. Orv.hetil.
102 no.8:353-~.-357 19 F161.
1. Pestmegyei Tanace Idegbeteggondozo Intezete es a Janos Korhaz-
Rendelointezet Bajme'gRIl&PitO Osztaly.
(TRAIQ,UILIZIM AGENTS ther)
(IMPRESSIOM ther)
(PSMIOdES MANIC DEPRESSIVE ther)

dr.
"Suggestion" by Barthold Stokvis and Manfred Pflsaiz. Reviewed
IT Istvan Hardi. Magy pszichol szemle 21 no. 1: 133-134 164.

E'-CFRPTA MEMCA Sec 16 Vol ?/5 Cancer FAY 59
i8j,j. Studies of cervical carcinoma with the phase contrast microscope
Die Utticusticlitim, I I
,(-it drr l'ortioUrzin(iiiie Iiiii I lilfe der Phasetiki Pitt ra~,tni'krf A,(i-
S%'I.JI)A.J., HARDIA~.KA NL alld I'I-A(~Ko\-A B. Valli. -Aijat. hist. inid Otiki)l. Inst.,
Med. Fak der Briiiiii Geburish. Gvniik. 3938, 1511,1:2 (11):)-200)
Pliase cowrast znicr'oscopy %vas citiplov"I it' exallii'latioll (if 357 We"11'ell. 111 226 out
fir 2';(') Cast's ((5-7",,), Cervical ill- villvar carcinonia %vas dia-tiosed. fit 86", pliase
cotitrast niicrowopyallmved iininediate diagnosis of the histological hif-iiily if)
Ihe fin't Cytological exaniiiiation \vas Falsely ticgativc. Oil accouilt or
it5~siinl)firitv and quick applicability, pliase contrast Illicroscopy is suitable for exa-
IIIIIIati(itis ill screening clinics. Becatisr ill(- characteristics ol'iiialigiiancy are not al-
ways oittspoken lihase coittraM ititcroset Illy is .111 aktxiliary liteflu'd, '.0lich Itkitst 1w
list-d oilly ill f-IIIIII(Ttioll %vitil other nictiiotis orexaniiiiatioti. it aii,)%vs Oinvi-vation (,r
dir reillilar chati"es during irradiali(iii ireatinent, as was done ill i,)6 patients. III
collibillatioll %Vidi llistoclicillical and cyt(icliciiiical inctliods it nialics the chatiges ill
living cells visible and thus constittitcs;t valuable contributioii to the studv ofdisitir-
hances title to irradiation.

HARDT . D.
Present stage and immediate needs of typifying. Constr Buc l/. no.
672:193 24 N 162.
1. Arhitect-sef al sectorulviL de Upizare din I.S.C.A.S.
.0
I

IAROVICI, M., candidat in stiinte economice; COSMA, M., ing.; DODU, A., ing.;
MAGOVEI, M., ing.; GIURCA, Virginia; HARDT, Hedi, ing.
Aspects of the comparative economic efficiency of the main textile
technologies. Ind text Rum 15 no.11:573-580 N 164.
1. Institute for Textile Research, Bucharest.

fjj4-JDT I.T.
"Electrification of railroads in the U3311.11
P. 382 (Electrotehnica) Vol. 5, no. 11, Nov. 1957
Bucharest., Rmania
SO: Monthly Index of East Europdan Accessions (E---AI) LC. Vol. 7, no. 4,
April 1958

HARDT, N. - -
SUFLU-1E., Given Names
COuntrY: Rumania
Academic Degrees: Engineer
Affiliation: -no t given-
SOurce: Buchare st 2 Sti inta sl Tehni c a 9 No 8 , Aug 19611 pp 22-23.
Data: "Food Refrigerators."
Gpo 9a1643

imur, H,, Ing.
Commercial automats. St A Teh Buc 14 no. 7;42-4.3 JI 162.
i T; r i
~ t. ,

HARDT, I L. -
Improving the performances of ice generators. Ind alim 14 no.
lOt/+16--~420 0163.
1. I.S. "Frigotalniicauz,Ducuresti.

MAGI, Heino; HARDUVA, E., red.
[Otte~aa]Dteplrit- Tallinn, Eesti RiMil- Kirjastus,
1963. 101 p. (In Estonian] (MIRA 17-.6)

S/19 61/003/001/019/020
B1 19YB216
AUTHORS: .-_Harky_,_D., Spiegel, V., Nytrai, K.
TITLE: Synthesis and polymerization kinetics of the complex vinyl
ester of. -salicylio acid
PERIODICAL: Vysokomolekulyarnyye soyedineniya, v. 3, no. 1, 1961, 144-149
TEXT: Vinyl salicylate (VS) is of interest as initial material for polymers
inasmuch as it possesses both an OH group capable, under certain conditions,
of entering into polymeranalogous reaction and a mobile E atom which may
possibly intensify the polymerization reaction. In contrast to other
authors who obtained 2-methyl-4-keto-1,3-benzodioxane on transesterification
of vinyl acetate and salioylic acid, the authors of the present paper
obtained VS in 10.4% yield by reducing the reaction time (from 36 to 3.5 hr)
and lowering the reaction temperature (to 73-820C). The data of VS arei
boiling point 1250C at 3 mm. Hg; nonfreezable in an acetone - dry ice mixture;
molecular weight 176 (determined cryoscopically in benzene, theoretical
molecular weight 164); MRD 42.96 (theorY 42.87). Further evidence of the
Card 1/3

Synthesis and polymerization...
S/190/61/003/001/019/020
B119/B216
structure of VS was gained from its infrared spectrum (Fig. 1). Azoiso-
butyronitrile was used as initiator in polymerization tests of VS. The
polymerization kinetics were followed dilatometrically (using an ampoule
dilatometer with a capacity of 10 ml). The molecular weight of the polymers
was determined viscosimetrically (the polymer was hydrolyzed in methanolic
NaOH and the polyvinyl alcohol obtained dissolved in water and then
measured). Results: The chain transfer constant of the monomeric molecule
CM is 8.0-10-3 at 70 0C (CMfor vinyl benzoate, having no OH groups,is
ro., 7-10-3 at -800C, GM for vinyl acetate is -0-15-10- 3 at 600C). Reaction
mechanism: P' + CH CH ---4 P i+CH = CH
2 1 2 1
#i 0 -CO 0 - CO
OH
U
Card 2/5

Synthesis and polymerization...
CH2 = CH
0 - CO
0*+
CH2 - CH
U - L;U
OH
S/190/61/003/001/019/020
B119/B216
CH 2 =CH
CO
O-CH 2- CH'
0 - Co
OH.
is
The overall activation energy, E, of the polymerization reaction
27.7 kcal/mol. The authors thank D. Varsanyi and S. Golli for their co-
operation (infrared spectra). The study presented is a part of the work
for a diploma by the second author, April 1956, at the Department of the
Technology of Plastics and Rubbers of the Budapest Polytechnic Institute.
There are 6 figures, 2 tables, and 11 non-Soviet~bloc references.
ASSOCIATION: Research Institute of Organic- and Plastics Industry, Budapest
SUBMITTED: September 14, 1960
Card 3/3

S/19 62/004/012/013/015
BlOlYBI66
AUTHORSs Hardy, D.,
tray, K. , Fodorova, N. , Kovacs, G.
TITLEs Polymerization of cetyl methacrylate
PERIODICAL: Vysokomolekulyarnyye soyedineniyd, V. 4, no. 12, 1962,
1672-1878
TEXT: Polymers with a vitrification temperature of 20-250C and an
intrinsic viscosity of 1.60-".45 were obtained in the course of a study
J
of the polymerization kinetics of cetyl methacrylate in the presence of
benzoyl peroxide in N 2 atmosphere at 50-800C., The degree of conversion
was a linear function of time. Polymerization ceased at 66$' conversion.
No region of accelerated polymerization was observed as with other
acrylates and methacrylates,. The following data are given; constant k
of the initiation rate, 3.09*10 -6 ; constant k of tho chain-6rowtb,
1/2 9
98 at 30OC; k 9/kt - o.o65 at 300C, 1.080 at WC, where k t is the
constant of chain termination; furthermore, k 9/kt 112 _ 42.3 exp(-2500/RT).
Card 1/2

S/190/62/004/012/013/015
Polymerization of cetyl... B101/B156
The gross activation energy of polymerization is 17.8 kcal/mole, E 0.5 Et
- 2.4 kcal/mole (E,, . activation energy of the chain growth, F.t- activation
energy of termination). The-chain transfer coefficient, Chi tit 70'C in
1-4*10-5 for the monomer, 9.83-10-5 in the presence uf MV and
20-5-10-5 in the presence of isopropyl benzene. The initiation efficiency
f is only 0.14. Theoc low values, as compared with other acrylates and
methacrylates, are explained by the high molecular weight and the high
viscosity of cetyl methacrylate. There are 4 figures and 4 tables.
ASSOCIATIONs Nauchno-isslodovatel'skiy institut plastmassovoy
promyshlennosti Budapest (scientific Research Institute of
the Plastics Industry, Budapest)
SUBMITTED: June 16, 1962
Card 2/2

C' HARDY., Erno, okleveles gepeszmernok; HARDY, Ervin, okleveles gepeszmer-nok
Economical regulation of condensation temperature of cooling
installations. Energia. es atom 13 no./+/5.-217-219 Ap..IV 16o.

Erao, okleveles gepeszmernok; HARDT, Ervin, okleveles gepeszmernok
HARDY$ - -- ~ I--------- --- - ... - - -.-
Economical regulation of condenBation temperature of cooling
installations. Energia es atom 13 no.4/5:217-219 A?..vo- 160.

1~~M_Readti=SZjjj2L the I. - - -- . .. Q,
FCL14P16T1=jU= crt. Vixyles_tqisland Investi-
g4tion of' Their CorreUtion -With A-c'id, Rzidleals .I ~nd_ J. 'S'zita
tOentral Research Institute for a
2. dhemistry. Hun __~"Aca#e,
-garian Aca__eMr of Sclence
Budapest; Xeceived October 2, 1956
Acta Chimica-Acridemiae LeLt.-iitix-um Huncuricue
1958, Vol 15, Nr It, f .3 3 1
Distv 4F,3d/4F.4j/4E2c(-j) SUMMARY
1. It was found that a correlation exW% ijetween the elcerrwic of the obwlkltc value of
the rule constant of the initiation reaction ond the flecrease of scidity of the corresponding
fatty acid, measured at the same temperature. in Ilia case of the vinyl caters o(sliphatic fatty
aelds, The value of the appropriate action ranstants diminished by IncrenAing molecular sizes
of sulistituents, whilst the absolute values ofinitiation activation energien proved to be identical
within the errors of mea~urcment, ranging about 33 000 cal.-
2. On the basis of literature data the theoretical and practical firnits of the Inhlbif6u
met6A were established. It was stated that this method of measurements does not take Into
consideration the capability of irfitistars to form radicalsand theftner mechanism of theinitlation
process, either.
WHII MIR]

h%c (V 4E
4 tion 01,*gLeAtem
the
in
s!
Ir 'm ~Aca I
and invextiptlon of Wk C as it
GL~= and J. Silta (H DuzvpLst~.,
hmw English
-The behavior of a vt;VI polylzer In the initlatlow rtmetion
of a polymerization pri>." should be detd. by the coudira
tion of the w-liond of tho vinyl group. The validity of th6,.2 Mal
presumption was _xtudlel by an investigation of Wt6t on
reactions by the Inhibition method and K*Art'g_
C.A. 44, Mj),,by using azodilsobutyronitrile as the ln~
Itiator and 2,"IphinyL-I-PkrYIhYdrazyI a3 the inhibitor.:
'In the series of the vinyl esters of formic, acetic, proplouic,'
butyric; isobutyric, and isovaleric "a, the trend of the-
reduction of &be. magultuAts of rate cousts. of the Initiation.
reactlotiat the same temp. was Identical to the trend of de-j
.-crease of the disawn, consts. of the fatty acids. The in-s
Iltiation activation 'energies were Identical., A differtut!
.-behavior was found with vinyl monochloroacetate and rinyt
ibeazoate. Ali atteniptis at radical polymaization of the
~vinyl furoate failed. Two new vinyl esters were syntbe-1,
'4zed and had tht followla q6: furoate~ to, 14-144'.
b. IS"', dr; 1.1127 I.Owtymul
M., 'VISM
b. 104-6% d1': 0,8921, n-j? 1.40U. A red MtOon rate
~detd. by the inhibition method only when the free t~8
formed on decompn. of the initiator reacts with a MO
Arthur Flelsilut-i

14 "1",
I

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l
i
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I bV?,,U- a 2 1

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-
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17
58)
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Acta hint. Acd3.
,

te and azodfisobutyrn-
-Mixts. of vinyl aceta
(in German).
~nitrile with turancurboxylic." vinyl ester (1) or foral

,
' phenyl estir (H) were pol irized In s~alecf
-Mboxylic acl ynt
r
the absence - ..'.1naeasing
80*
'clitat.meters at -of 0.
in
.
.
amts. of I aud H greatly InWbIted the rateof polyuierivt-~
in

j 4E26(j)

Elk y

IA

L
j
W
d

:A fa.' ln,,stlgallon
of the effect of vinyl luroate and some
.
derivatives on polymerization proctsaics of radical mechanism

e
It 11 D. D at v i d, K. N %, i 1, r a L 11. 1
~j ~,, 04, LIMS, 7o--TW, -pp ;,
t
d
o
s a;,8 rig..
e
invoilLignLion athowM Malt filran derivativo. bavil a

j.41m..g n't""ling infilleor. ast. till, imad;
call tylat, I 1~
air neeta(clabiro the Foram ring renels Willi lilt, Inl4l.
islitiq 'Iret, rit-lit-M. Kinetic. menstiretrionts of polyinvrizaktinis
Ii at it tl(iitalo rhaiii-trousfer hibilallinn Firatt
A iiii! otivi o4er or iitrallydrofil"Illen rim X3, lit, livid wn" hyll-
llw:-i~otl and pallymorlAcd. lit file cast; of tolmlij,drofuralan flari.
vativon no rulartlitig ofibel, oil the railical polymerixattion or
vmYl Amin wait- oWrved. Ala a cootitatlooneo it'follown that,
Ilic' hark of Ula i-ndical pol)-moriank nit of vinyl fitruaLo is
'i-xiihiiiii-il lky the fact 01al, lito furnin ripig of tho monomer
Ini'loetilo rl'LIVIH with tho initiatinit two radicals and thim nit
::noluhihibitimi of Ojo nulical polymeriyation twntint. ThiR In
a, .,are nju, or similar laionosm-oot, hoing.

l
MiArt-vi,(L oifly ill that inantiout; of rruis milieniat ith KIIYI
y
b
uty~:ano)
141loptiontli; orsomoolefincei(octonc.l. propyinuo. isu

'V4~j! AP!,
7
jelisq,
to We XWte 01I
16filza CA 0
gl
iza& r7limce a a Bm
-gqg~ww I, ab lAW WUO
oft T19j. 9 rjo i . the
'a
yso
ungFrIVIPIR W__
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-W
I
car 94
4 ' '4 0'4';vu-
ied VU + b
the" 0
ra clicl, tho TV
461 "the inav.
ci C. AVAG -1, qnts-~
qlF ton cc 40 41
P. ard.A
M. qo
hsew~V4 to
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on.
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OR.
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y Z., Uri,, r- ;-Y
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k-,if~12
G

Of tile Plastics, Jk-jdus,~,:-v
i- in. g
ary
O~IG
. Pi, S. Kagyar kem. -)%.a pj a 13. No 7-E, P-2 7 0

3'TRACT
'
Devel,)Pmerlt trends
of th
6
h

-f
o
are consi-1
derrad ungariap industry
-
. L. Pesir.
Research on materi-als at t"10 He:~ea-rc;, lns Of L)"C
Industry and Plastic Materials Indilst'7- p. 67*
U
~L~GYAR KF,~jKiS,,)F,. LAPJA. mik,,sok FCyesiilete) P,,-ingary
i ya r K,,
Vol. 11t, no. 2/3j Feb./,%L3r. 10/59-
1-Tonthly list of East European Accessions (EEAI), IL, 1101- P, 110- 81
Antust' 1959.
Uncla .

Distri 4E2c(j)
170160. 66.095,26,
Investigausa, of "MGM Pely"Wrizatio processes In the,
pre"Res of sues substancu-7T juteat at orswao ha. i
logen compounds an the poqmdzauoa of vinyl saotsia.i
(In Russian) A. W a h n a a h I
Old
imical A" T
No. S. pp. 241-272. 6 fixa.. 6 tabs.
The chain transfer constants of 30 different organic!
halogen compounds were determined by the authom at
100 0 in the polymerization of vinyl acetate promowd by
benvoyl peroxide. Of the examined 30 organic halogen com.!
undo, halogen hydrocarbons possessing hologen-carbon'
C
da of low binding energy, a. g. biromoforza. tatrabromo-i
methane, monabroma-triclilaromathane, proved to be the.
most active. Furthermore, the authors established the cor.
relations In the various groups of compounds @!!Mon
derivatives of matharte. ethane. ethylene, aliphatic anti are.
matio halogen derivatives. oxygon-bearing halogen deri.,
vatives) between the structure or organic substances Ind
the chain transfer activity observed in the radical poly-
Merization of vinyl acetate.

Distr: 4E2c(J)
171J60. (16,001.0
1
llovestigation of radical pS!jMjfljE!!M processes In the
resoncio of &USA substances. It. Effect of hydrocarbons,
:1cohols. aldshydes. kotoBes, eaters anik acids an the poly-
Morization of VlnyI acstatsv.,f(In Russian) A. NV it h Tj~"h , ; A t I/--.dw(-!3
Acia Minsica AcadewioFlgc-ie~linruon Huvt*
rjricue, VW_. 20, 1069, No. 4, pp. 381-391. 5 figs., 5 'tabs.
The chain transfer constants of 33 different organic
compounds not containing halogens were detcrminod by the
authors at 70P C la the polymerization of vinyl acetato prr.
meted with bentoyl peroxide. Of the examined 33 diffurvi.t
organic compounds not containing Mogena. some substances
containing extremely labile hydrogen atorno - a. g. 9-phanyl
nuorena, benayl mercaptan and dimcdon - proved to be
the most active. Furthermore, the authors established the
correlations In the various groups of compounds (hydro.
oarboruh alcohols, sildehydon, ketones, esters and acids)
between the structure of organic compounds and their chain
troxisfer activity In the radical polymerization of vinyl
acetate. In the some compounds the maximum absolute
values of the observed chain transfer constants appeared
in vinyl aostate, while the minimum values wore found in
styrona..No changes could be observed In the sequence f
chain trounfer activity of the various monomers.

DOBOY Janos;,HARDY, Gyula,__akemiai tudomanyok kandidatusa
Some problems relating to radiation polymerization.,Kem tud kozl MTA
14 no-3:330-336 160. (ERAI 10:9)
1. Szerves Vegy1pari es Muanyagipari Kutato Intezet, Budapest.
(Radiation) (Polymers and polymerization)
(Ethylene) (Ion exchange) (Chloroetbylene)

HARDY, Gyula
Data on telomerization reactions. Magy kem lap 15 ro.?:307-314
JI 160.
1. Szerves Vegyipari an Muanyagipari Kutato Intezet, es "Magyar
Kemikusok Lapja" szerkegzto bizottsagi tagja,

KORANYI, Oyorgy, dr.; GYULAY, Zoltan, egyetemi tanar; DIOSZEGHY, Daniel,
ef,-yetemi tanar; WAHLNER, Aladar, fomeraok; VAMOS, Endre, kandidatus;
NYUL
=j.j _ a, kandidatus; FREUND, Mihaly, dr., akademikus;
mer, akademikus; TAKACS, Pal, dr., kandidatus; SCHLATTNER,
'~Iefi-b,-I~~didatus; HARDY, Gyula, a kem:Lai tudomanyok kandidatusa
Raport on the 1959-60 work of the Committee on Petroleum and Coal
Processing, Hungarian Academy of Sciences. Kem tud koal MTA 16 no.3.
349-359 161.

11/006/62/000/002/001/002
D249/D303
AUTHOR~ Hardy, Gyula
TITL&. The chemical effects of high energy radiationj prospects
of its application in the Industry
PERIODICAL. Magyar k9mikusok lapja, no. 2, 1962, 52-61
TEXT- A short review of the application of radiochemical techniques in
the chemical industry, based on Soviet and Western work. A brief des-
cription is given of radiations and of the main. types of radiation sources.
Radiochemical techniques finding extensive applf;cation in- the plastiCs in-
dustry are described and discussed under.. (1) Polymerization in the solid
phase as a technique for preparing sterecapecific polymers. Examples
of radiochemical polymerization in the liquid and gas phased are mentioned.
(2) Transformation of polymers, eog. radiochemical chlorination, sulpho-
chlorination and sulphoxidatiOD*(3) Radiochemical grafting,, (4) Cross-
linking of polymers. Since this can be achieved by irradiatingfinished
products (e.g. foils, plates, tubes) it is a field of appl--'cati3n which
Card 1/ 3

f 1/006/6 2/000 /002/001/002
The chemical effects D249/D303
has been studied most extensively by the industry. (5) Radiochemical vul-
canization. The introduction of radjacbemical techniques into the petro-
leum processing industry is thought to promise considerable savings,
expecially when processing a large volumes of materials. Reference*is
made to studies of the rad-iochernical cracking process made by Topscief
andico-workers (Ref- 20-. Lecture at the Conference on the Application of
the Sources of High Energy Radiation 1-9 Industry. Warsaw, 8-12 September
1959)9 who concluded that above 2300C radiochemical--thermal cracking was
a chain reaction. The composition of the products iis identical with
those of the thermal cracking while the yield is much larger~ Further
potential application in the petroleum industry is the de-Rulphurizat-Jon
of petroleum productso Radiochemical techniques Ln the synthttf-r. organic
and inorganic chemical --ndustrie8 art briefly reviewed, The lines of
application indicated are preparation of nitrit: acid, hydi-az:.ne, sul-
phuric acidg hexachlorohexane, phenol plus telome:rizaTion. -eactlons.
Finally, the fuirther technical and economic problems of indmetr:ral appli-
cation are listed. These ar&- (1) Inadequate utilizatlor. of tl~e energy
of radiation sourr~es. 12) Produciion r~f hemogenecus fields of radiation
Card 2/3

H/006/62/000/002/001/002
The chemical effects o.. D249/D303
in large volumeso (3) Finding sensitizer# to reduce the duration of
irradiation required by some reactions. Finding methods to increase
the selectivity of the radiochemical reactions. (4) Finding the optimum
conditions for the radiochemical reactions requiring large amounts of
energy. (5) Removal of the products of the reactions from the field of
radiation before changes start due to a further amount of undesir*d
radiation. There are 5 figures and 29 references: 14 Soviet-bloc and
15 non-Soviet-bloc. The 4 most recent references to the English-
language publications read as follows: S.H. Pinner, British Plastics,
34, 30, (1961); Charlesby and Arnim: J. Polym. Sci., 26, 151, (1957);
H.A. Dewhurst: J. Chem. Phys. 24, 1254, (1956); McBee, Roberts and
Puerckhauer- J.Am.Chem.Soc.9 79, 2329, (1957),
ASSOCIATION. Wianyagipari Kutatg Int9zet (Industrial Plastics Research
Institute)
Card 3/3

HARDY, (~rula; SZAPk), ZoltRn
Technical-economic reviews. Mnpv kem lap 17 rr-2:102-103 F 62.
1. Miuarvagipari Kutato lirvtozet (for Hardv) 2. "Magyar Kemikusok
Lapjall azerkeszto bizottsagri tagrja.

HABDY, Gyula
Technical economic review. MAU kem lap 17 no.3:112 Mr 162.
1. *Magyar Kemikusok Lapja" szorkeszto bizottsagi tagja
I ~ i I -:']. - ~ W
., , ~'. x
, , .1. -~ . !
. ft I , :-*,!, 1j-~ ~ 1 1 - ;
~! I I .. ~. I '~ I -;": ; - 1 1 . .. .

HARDY, Gyula
New aldehydes prepared from diazonium compounds. Magy kem lap
17 no.6:270 Je 162.
1. "Magyar Kemikusok Lapja" azerkeszto..bizottsagi tagja.

HARDY ,--, Gyula -
A new sulfonation process. Magy kem lap 17 no.6:270 Je
162.
1. "Magyar Kemikusok Lapja" saerkesato bizottsagi tagja.

HARDY, Gyula
Technical economic review. Magy kem lap 17 no.6*-273 Je
,62.
1. "Magyar Kemikusok Lapja" szerkeszto bizottsagi tagja.
NIa-':;.'-i - I :
.1. f- I ~
I

I Iii-iRDY G-,aila
'-Z~y -- -
liew hydrodealkylation process. Magy k-em lap 17 no.8:353
Ag 162.
1. "Magyar V'.or.-i,'.usck Lapjall Szf,-rkeszto bizottsagi t.I.-ja.

IUCIDY, (11)10-a
Recovery of hydrogen from the fuel gases of petroleum refineries.
Hagy kem lar. 17 no.8:353 Ag 162.
1. "Magyar Kemikusok Lapja" sztrkeazto bizottsagi tada.
;P!", 'It H -r-:1-
i~ 1; - j 1 1 - .: : 1 -.1 1 1, ~
~ - I .

HMY J. Gyula
A new electrothermal ploco-'Is to produce al-aminiza.
Magy kem lap 17 no.8;~81-382 liF W-
1. %Magyar Kemilvisok Lapja" szerkeszto bizottsagi tigja.
4~

HARDY, Gyula
'- ~ApplyingmKecule screons at alkylations catalized with
acids. Magy kem lap 17 no.8:382 Ag 162.
1. "Magyar Kemikusok Lapja" szerkeazto bizott4ag! tagja.

HARDY, Crtaa
New process for preparing malic acid. Magy kem lap 27 no.9099 S 162.
1. "Magyar Kemikusok Iapja" szorkeszto bizottsagi tagja.

HARDY,_ _G _ la
p
Preparation of dicyanide from cyanide hydrogen and nitrogen oxide.
blagy kem Up 17 no.9.-399 S 162.,
1. Ollagyar Kemikusok IApje szorkeazto b12ottsagi tagja.

._~, Gyula
Putting a now dev-ice into operation for extracting oil seeds. Magy kem
lap 17 no.10:444 0 1.62.
1. "Magyar Kemikusok Lapja" szerkeazto bizottsagi tagja.

_~ART,_Gyula
Oil wells controlled by calculating machines. Magy kem lap 17 no.10:
44.4 0 162.
1. "Magyar Kemikusok Lapja" szerkeszto bizottsagi tagja.

HARDY, Gyula
Calculating machine for planning. Magy kem lap 17 no.lOt451 0 162.
1. "Magyar Kemikusok Lapja" azerkeazto bizottsagi tagja.

HARDY, Gyula
Now role of boron hydride in preparing catalysts. Magy kem lap 17 no.10:
472 0 162.
1. "Magyar Kemikusok Lapja" azirkeesto bizotteagi tagja.

Gyula
Anticorrosive coatings made of zinc silicates. Magy kem lap 17 no.10:
472 0 162.
1. "Magyar Kemikusok Lapja" szerkeszto bizotteagi tagja.

~I ...-; M',,, 111MI 11"I". ~, ~!: -, I.- --.- - . .-
HARDY, Gyula
Now analytical instruments and processes. Magy kem lap 11 no.11:
1*87 N 162.
1. "Magyar Kem4msok Lapja" szerkeazto bizotteagi tagja.

ERDEY-GRUZ, Tibor, akadeiaikus; BRUCKNER, Gyozo, akademik-us; LENGYEL, Bela;
TELEGDY-KOVAIZ, Laszlo,, a tudomanyok doktora;
kandidatus; GEREGS, Arpad, akademikus; FOLDI, Zoltan; WOLKOBEF,
Zoltan; TUDOS, Ferenc, kandidatus; PUPDIAN,"Jeno; KRAUSZ, Imre,
kandidatus; ERDEY, Laszlo, akademikus; SCHAY, Qeza, akademikus
An account of the 1961 work of the Section of Chemical Sciences,
Hungarian Academy of Sciences. Kem tud kozl 18 m-3-.343-394
162.
1. Magyar Tudomanyos Akademia Kemiai Tudomanyok Osztalyanak titkara,
es "A Magyar Tudomanyos Akademia Kemiai Tudomanyok Dsztalyanak
Kozlemenyei" szerkesztoje (for Erdey--Gruz). 2. Akademiai levelezo
tag (for Lengyel and Foldi). 3. OA Magyar Tudomanyos Akademia
Kemiai Tudomanyok Gaztalyar+k Kozlemenyei* szerkeszto bizottsagi
tagja (for Bruckner,, Frdey., Foldi, Gerecs, Hardy, Lengyel., Schay,,
Tudos).

I - ',- 1"..
` V11 1111". w - ". - I' ~' 11- -, , , , ". . , ~ - . . .
HARDY, Gyulane; RADICS, Wos; TUDOS, Ferenc., kandidatus
An account of the 5th International Symposium on Free Radicals.
Kem. tud kozl 18 no.3:509-519 162.
1. Magyar Tudomanyos Akademia Kozponti Keraiai Kutato Intezete., .
Budapest. 2. 'A Yagyar Tudomanyos Akademia Kemiai Tudomanyok
Ooztalyanak Kozlemenyei" szerkeszto bizottsagi tagja (for Tudos).
0

RARE&, ayula
A new method of separation: permeation in the liquid phase,
Magy kem lap 18 no.1:7 Ja 163.
l@, wMagyar Kemikusok Lapjaw szerkeszto bizottsagi tagja.

HARDY, Cy-u'-a, dr.; VARGtl, Joz~sef
Investigationz. in the field of' radiatIon.-Jnduced golld state
polymprizat-ion. Pt. 2. Acta chimica Ifung 40 no.4:419-430 164.
1. Chair of FI-1.stics and Rubber, Technical liniversity, Budapost,
XI., Budafoki ut 4-6. 2. !-k4itortal bi-ard. jme.,nbp:, I'Acta Chim-tca
Academiae Scl-ntfarurn Ilaunricne" (for IIIII-dy).

HARDY.,, Gyula
Po y-(-~&xafluorprojrylene) plastics materials. Magy kem lap
18 no.l:ll Ja t63,
1. R4agyar Kemikusok Lapja* bizottsagi tagja.

HARDY, Gyula
More durable thermoelements. Magy kem lap 18 no.1:32 Ja 163.
1. 44agyar Kemikusok Lapjaw ozerkeazto bizottsagi tagja.

HARDY, GpLla
Electronic device for reading manuscript mLmb-,-rs, Magy kern
lap 18 no.1:32 Ja 163.
1. *Magyar Kemikusok Lapja" szerkeszto bizottsagi tagja.

-W
.1
HARDY, Gyvla
A new ion-exchanging resin for desalting proteins. Magy kem
lap 18 no.1:42 Ja 163.
1. OMagyar Kemikusok Lapja* szerkeazto bizottsard tagja.
0

HARDY, Grila
M-Iined metal drum. Magy kem lap 18 nool:42 Ja 163c.
1, wMagyar Kemikusok Lapja" azerkeazto bizottsagi tagja.

HARDY,, Gyula
Inorganic polymerao Magy kem lap 18 no.1:52 Ja 263.
1. *Magyar Kemikusok Lapja" szerkeszto bizottsagi tagja.

-q HARDY. Gyula.
Technological and economic reviews. Magy kem, lap 18
no.5%245 W 863*
lo "Magyar Kemikusok Lapja" szerkeszto bizottsagi tagja.

HARDY, Gyula
A mq antirnialstrial drug. YAU kem lap 18 no.6:253 Je 163.
1. "Magyar Kemikusok Lapja" szorkento bizottsagi tagja.

- UMIA11GELa
.
strengthened by glass fibers. 14agy kom lap 18 no.6:265
Rubber
.To 63.
1. OMagyar Kemikusok Lapjal azerkeazto bizotteagi tagja.

H4QY qpla
r, - ft . Q _ Mw
Development in the production technology of fertillizera. Mag7
kem, lap 18 no.6:275 Je 163.
1. "Magyar Kemikusok Lapja" szorkeazto bizottsagi tagja.

HARDY, Gyula
Rftwval of the radioactive 'mPur'ties of milk by alectrodialysis.
YAky ]on lap 18 i4o.6.-288. Jw 163.
1. wMagyar Kemikusok Lapja* szerkeszto bizottsagi tagja.

RAWY, Gyula
Some questions relating to the tasks of the plastics industry
research in Hungary* Magy kem lap IS no.7:29-7-300 J3. 163#
1
1. Naanyagipari Kutato Intatet; *Magyar Komikusok Lapja"
szerkeszto bizottsagi tagjao

RMT, Gyula
Now method for preparing especially fine metal powders. Magy kem.
lap 18 no.8:383 Ag 463.
1. "Magyar Kamikusok Lapjau szerkeazto bizottsagi tagjao

HARDY) Gyula
Removal-of carbon oxides from lighting gases. Magy kem lap
18 no.11:554 1-1 163.
1. "Magyar Kemik-Lisok Lapja" szerkesvto bizottsagi tagja.

IIAIWYI Gyula
Synthesis of protein-vitamin concentrates from petroleum
products. Magy kem lap 18 10-11:563 11 163.
1. "Magyar Kemihisok Lapjall s7erkeszto bizottsag., tagja.

HARDY, Gyula
An improved process for hydiazine synthesis. Magy kem. lap 18
no-1-1:565 11 163.
1. 111,Tagyar Kemikusok Lapjall szerkes7t..) bizotts--gi tagja.

HARDY,, Gyula
Chemicals in space flight. Magy kem lap 18 no.11:568 IT 163.
1. "Magyar Kemikusok Lapja" szerkeszto bizottsagi tagja.
. !.-- , , , , t , I . . i '. ... ~ .
! .. : 1. :. -13 : I -
.1 1 . ! ! I

HARDY , Gyula
Synthesis of cis-olefins by the I-littig method. Magy kem Ia-p
19 no.11:568-569 11 163.
1. "Magyar Kemikusok Iapjall szerkeszto bizottsagi tagja.

HARDYI Gyula
.1-----ILII-,-
Regeneration of pickling solutions of metal works. Magy kem
lap 18 no.12:576 D 163.
1. n1lagyar Kemikusok Iapjall szerl:eszto bizottsagi tagja.

HARDY, Gyula
New, specific glasses. Magy kem lap 18 no.12:588 D 163.
1. "Magyar Kemikusok Lapja" szerkeszto bizottsagi tagja.

HARDY, GyuIA
New antibiotics& Magy kem lap IB.no.12:592 D 163.
Semiautomatic device for simr.1taneous analysis of coal, hydrogen and
nitrogen. Magy ker, lap 18 no.12092 D 163.
Continuous reactor for prep.tring carbon disulfide. Magy kem lap 18 no.
12:611 D 163.
1. "Magyar Kamikusok LaDjull jzcrk-mszto bizotteagi tagja.

IT-A.M. Gyula
Polymerization of benzene to phenyl. I-agy kei--, lap 1,'
no. 12; 597 D 163.
1. 'Tagyar Kerilikusok Lupja" :jzcrlteszto bizottsa--;i tagja.

--HARDY, Glyula; NYITRAI, Karoly; FEDOROVA, Natalia; KOVACS, Gabor
I Cetyl-methacrylate polymerization. Magy keim folyoir 69 no.l:
42-46 Ja 163.
1. Mianyagipari Kutato Intezet, Budapest.

RMY, Gyula; NYITRJY, Kaxoly; KOVACS, Gabor; FEDO'.1,011,'I, flatalia
Research in the field of solid-phase radiation polymerization.
Pt-3- Magy kem folyoir 69 no.10:447-448 016).
1. MunnyagiFari Kutato Intezet, Budapest.
;_:~ !
- q . ~ T, 1 'F! 1:
, ;~ I I ~ - I

HART)v , Gyula
Foin.ation of anhydropenicil-lin by molecular rearrangement.
Magy kem lap 19 no. 4r184 Ap 164.
Research and development expenditure growth in the United
5tates. Ibid.:188.
New me-thods for the epoxidation of olefins. Ibid..-195.
1. Editorial board member, "Magyar Kemikusok Lapja.11

HARDY, Gyula; NYITRAY, Karolyi KOWCIS, Gaboi-; Natalia
Research in the field of solid-phase radiation polymerization.
Pt.l. Magy kem folyoir 69 no-10:437-441 0 163.
1. Muanyagipari Kutato Intezet, Budapest.
I"

HARDY, Gyula; VARGA, Jozsef
Research in the field of solid-phase radiation polymerization.
Pt.2. Magy kem folyoir 69 no.10:441-446 0 163.
1. Budapesti Muszaki Egyetern Mluanyag- es Guniipar Tanszeke.
- I i
~~!i --i

HARDY,-Gyula
Method for oxidizing aromatic compounds. Magy kem lap 19 no.6:313 Je 164.
Growing chemicalization of agriculture. Ibid.:313
More efficient use of fertilizers. Ibid.013-314
Distribution of American chemists by specialization. Ibid.:314
1. Editorial board member, "Magyar Kemikusok Lapja.n
I V 14,

HARDY, Gyula
Spread of fermentation technologies. Magy kem lap 19 no.7:359
Jl 164.
Acetylene production in plasma rays., Ibid.'-365
Protein synthesis from hydrocarbons. Ibid.1365
Linear silicon-nitrogen polymers. Ibid.1365
Prospects for industrial utilization of the complete synthesis
of steroids. lbid.:390-391
Spray drying by air with reduced humidity. Ibid.:391
Antioxidants in food. Ibid.:391.
1. Editorial board member "Magyar Kemikusok LaDja.11

I Y. f7arga, 1.]
Kq~ATL, D, [Hardy, Gv~j~ VARGA,
Effect f adr~'-tlons on the solid stat=- zolymerlZa-,ion of N-vinyl-
3
S~accinjmide. llysokom.sced. 6 nc.9.172~-.117 3 S '64. (MIRA 17410)
1. Budapesht-skiy pol.itekbnicheskiy Instlitut., Venirriya.

,-_.Y_qDY _u .aroly; C,".JLIK, Istvan;
__,_PyjA; VARGA, Jozsef; NYITRAl, F It
ZUBONYAI, Laszlo
Synthesis, polymerization and copolymerization of vinyl-thio.
acetate. Magy kem folyoir 70 no. 4:174-179 Ap 164.
1. Renearch Institute of the Plastics Industry, BLidapest and
Department of the Plastics and Rubber Indtistries, Bizdapest
University of Technical Sciences.

HARDY, Gy-ula;__YARGA, joz.,3of
Investigations In the field of the solid phase radiant
polymerization. Pt. 4. Magy kem folyoir 70 no. 6-.258-264
Je 164.
1. Chair of Plastics and Rubber Industry, R-idapest Technical
University.

RT k"y
' 11 " ve t I c
Se- c Li y c r a d i on of a r~jm-, tl
'kem "af, ~~C nr.2:65 F '65-
Now Irstrumen', for meamxim-Y me-leculqr weight.
1. F:d-'LOrl,'Il Boa-d !Ipmber, "Hatzya-r Komilrusok TA~jj-.

HARDY, Gyula
New reactions with carbon monoxide. Magy kem lap 20 no.2:82
F 165.
1. Editorial Board Member, I'Magysr Kemikusok Lapja."

HARDY, Gyula
Direct transformation of hydrochloric acid to I-qdrogt:,,n and
chlorine. Magy kem lap 20 no.3:118 Mr '65.
1. Editorial Board Member, "Ragyar Kemikusok Lapja."

HARDY, Gyula
The new fluidization limektln built by the American Pfizer firm.
Magy kem lap 20 no-4:182 Ap 165.
Our plastics industry and chemical fibers industry in the last
20 years. Ibid.:197-200
1. Research Institute of Plastics Industry, Bndapest, and
Editorial Board Member, I'Magyar Kemikusok Lapja.11

-LL 1768h_66___E-TwP(j)j/1r-- "VI/M
W14
ACC NRt , T6009218 SOURCE CODE: HU,_
A 725W6 70 3766;z/5'D--176M
AUTHOR: Har ardi, DI. (Doctor; Budap 'est); Njjtra
d G a-Kh ZLjfaroly-Nitrai, K.
(Buda
(Bia ~P~ Gabor--Kovach, G. pest); Fedorova, Natalizi-i-IBudapest)
ORG: Re'sea"rc h Institute for the Plastics Industry, Budapest
I.,.TITLE-. Investigations in the field of radiation-induced solid-state polymerizations
Part 1: Cetyl methacrylate 45
SOURCE: Academia scientiarum hungaricae. Acta chimica, v. 43, no. 2. 1965v 121-128
TOPIC TAGS: polymerization, radiation polymerization, cobalt, polymerization rate,
polymerization kinetics, polymerization degree
ABSTRACT: :The kinetics of the polymerization of cetyl meth-
ra-c-'r-y-late was in ves.ti ga-ted in the solid state under irradiation from Co-60
'within the -195* toi:66*c temperature range..Owing to an increased degree of'
:Molecular mobility, the polymerization rate significantly increased at tem-
peratures near the melting point. There was evidence of solid-state phase.
,transformation at around -160C. Although radical inhibitors were found to be
effective, the polymerization reaction was considered to be of the anionic
degree was shown to be a function of cetyl mech-
acrylate concentration. Orig. art. has: 8 figures and 1 formula.
SUB CODE: 07 SUBM DATE: OqMar63 / OTH W : 007
Vj
Card

L 39548-66 EPF(n)-2/EWF(j)/T/EWA(h)/EW.t(.-i.~
ACC Nh: AP00Q3,;86
AITIMOR: Hardy, Gytfla; Nagy, Lajos
OR Pi e 'b_~,Ms ~11*t-tite for the Plast i cc I nj,m ~r ,_P;vtqF;v
search
Kutato Intezet)
-rly-wi par,
iation-col3olptieri-ation of" ac r--1 atil acid
TITLE: Solid-state rad r am- __~jr
SOURCE: Magyar kemiai folyoirat.,e. 71, no. 2,
TOPIC TAGS: coj2olymeriza,tio_T~11_ ',~(UaUon po1v11!iA,i-_-1! ir'll, 'I j. j
aliphati,c carboxylic acid
ABr,TPUICT: The solid system of acrylic amide and
acrylic acid has a phase-diagram with two eutectic pointa, and a wle-
cular compound of 1:2 molar ration Is present which has the highest mal-
ting point. The rate of copolymerization is the greatest in the cutectic
points, and goes through a mininum at the componition corresponding, to
the molecular compound. Orig. art. has: 3 figureo. 1,111
SUB CODE: 07 / SUBM DATE: 13Nov64 / ORIG TT',,F: 0~e'l
NWI-'-] D/(-,(;'[/ ',0!
[00, (jr/,,r/~
Card 1/1 llb

L 17000-66 EPF(n)-2/EWPQ)/T/EWA(h)/EWA(l)
ACC NR: AP6008605 SOURCE CODE; HUI(AJ'0511i,~/~')". 11VI/bil"
AUTHOR: Hardy. Gyula; Varga, Jozoef; Nagy, Cab.or
versity Blidapest.
ORG: Departm of Plastics and Rubber lnd~str 1-Technical Unt
(Muszaki Egyetem Muanyages Gumiipari Tanzzeke)
TITLE: Studies in the field of solid-state ation DOlYmerization!-Part 5:
Solid-state copolymerization of N-vinylsuc nimide an N-vifiyl-p~=rro idone
(copolymerization in solid and supercooled eutectics)
SOURCE: Magyar kemiai folyoirat, v. 71, no. 4, 1965, 171-175
TOPIC TAGS; copolymerization, solid state, radiation polymerization, supercooling,
heterocyclic base compound
ABSTRACT: Tbe eutectic mixture o 1he ingredients studied is 3.4 imide:
6.6 pyrrol-idone. Copollmerizati3grogressed at maximum rate with the
components in this ratio and at a higher rate in a supercooled.eutectic
than in a solid eutectic. The theoretical and experimental aspects of
the polymerization, And the.ch.aracteriatics-of.the.co.291 er., were
described in. detail.; Crig. art, has: 10 figtwese
SUB CODE: 07 SUBM DATE: 20064 / ORIG Rff: 005 OTH REF: 011
SOV REF: 001
Card 1/1

r ;if w i i yji,,iiTm h
L ~7001-66 1,;PF(n)-2/EWP(J)/T/ EWA(h)/JEWA(j)
ACC NR: AP6008606 SOURCE*CODE:
AUTHOR: Z.L,~Ga; Nyitrai, Karoly; Varga, Jozsef; Patko, Marton
ORG: Research Institute for the Plastics Industry, Budapest (Ruanyagipari ?~utato
Intezet); Department of Plastics and Rubber Industry,
Bu4A "e (Muszaki Egyetem Muanyag- es Gumiipari Tanszekej
TITIZ: Studies in t'he field of solid-stat radiation rigiaerizatioJ6 Part 6:
Ga-mma-radiation-induced solid-state polymelizaLlon ol V-1ny1 Iauraf.F_
SOURCE; Magyar kemiai folyoirat, v. 71, no. 4, 1965, 175-178
TOPIC TAGS: solid state, radiation polymerization, gamma radiation, monomer
ABSTRACT: Xaximum polyme'riz-ation rate was observed when the monomer's
temperature was near the Lialting point, + 3*C. The mobility of the mo-
lecules of vinyl laur4te at this irrature W45-considered to be re-
latively high. The polymerizationCtion was investigated under va-
rious operational pAKameters and in the presence of various compounds.
The results were prese~Eed_~_nddi6~_iisa6id_ifi detail. Orig. art. has: 9 figures.
(JFRS1
SUB CODE: 07 SUBM. DATE- 07Aug64 ORIG REF: 001 CTR REF: 004
Card 1/1

L 01195-66 E P F P~
ACCESSION NR: A 51 )_2/EVjp(j )/T/EWA~h)/EWA (c)A',,YA(1 2 CA
J~n
HU 000 Z~~" i/6oqoz5i~o,
515/07
AUTHOR: Hardy, Gyula; VSga, Jozsef
TITLE: Studies in the field of solid-state radiation RRIvmerivation. Part 7:
Effect of polymer formation on the kinetics 6f sol:-L-d--phWK6'-I~6l~Fma-r-lzation
SOURCE: Magyar kemiai folyoirat, v. 71, no. 6, 1965, 251-254
TOPIC TAGS: radiation polymerization, polymerization kinetics, polymer, solid
state, monomer
kBSTEtACT: [Authors' English summary, modified] The effect of the formed
polymer was studied in monomer-polymer systems during radiation-induced
solid-state Polymerization, on the kinetics of the solid-state polymeri-,
zation of N-vinyLsuccinimide.,~The formed polymer accelerated the polyme-,
rization, owing to deformatio in the crystal lattice (partly decompo-
sed crystal structure) and by the increased mobility of the monomer mo-
lecules caused by the polymer formed. This effect is likely to occur in
the case of monomers that are of accelerating character in solid-state
Polymerization. The re4erse effect is likely to occur in the case of
monomers that are of decelwating character. Origs art,, has:-'3 'aphs, I table
gr
Card 1/2