SCIENTIFIC ABSTRACT POLACKOVA, J. - POLAK, A.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001341710015-8
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: June 15, 2000
• Sequence Number: 15
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

ZALMN, X.; IHMCXR, B.; POLACWFA, -J.
--, ~,~
Cerebrospinal, venous and arterial pressure in intravenous administration
of massive doses of benzedrfne. Cae.lek.ceek. 90 no.19:583-585 11 Nair 51.
(Gin 20;8)
1. Of the State Psychiatric Hospital in Brno-Cernovice (Director-Nmil
Zalman, M.D.).

HAVLASEK, Ladvik, prof .,;,~OLACKOVA, Marle
On therapeutic exercise therapy in various gynecological diseases.
Ceak.cyn.26[401 no.1/2:64-67 J* 161.
1. 1. por.-gyn. klinika University J.Ev.Purlcyne v Brne, prednosta
prof. dr. L. Havlasek.
(GTHECOLOGT ther)
(EXERCISE TEMPT)

POLACKOVA, Marie; HAVLASEK, Ludvik, prof.
Gymnastics in prolapse of the internal genitalia and urinary --1n-
continence. Cesk.gyn.26[40] no.1/2:6&69 7 961.
1. I.gyn.-por. klinika University J. Ev. Purkyne v Brne, prednosts
prof. MUDr. Ludvik Havlasek.
(UTZR1- NE PROIAPSE the r)
(URINATION DIS I S ther)
(EXERCISE THERAPY)

POUCKOVA, %ris
250 yearn since the death of Ramazzini. Prr,--. lek.
16 no.1:37-39 Ja'64
1. Oddeleni latiny faulty vaeobt lp-],,-aT-: - "' "' Kar'. .. 11
university) v Praze; vedouc:~: doe. J.Kabrt.

MARTINGIK, Jaromir- POUCKOVA. Marie
1.
Preoperative and postoperative exercise therapy in prevention of
thromboembolic disease. Ceek.gyn.26[401 no.1/2:93-96 7 t61.
1. 1. por.-gyn. klinika University J. Ev. Purkyne v Brne, prednosta
prof.dr. L.Havlawek.
(THROMUMOUBM prev & control)
(SURGERY WMTIVE compl)
(EXERCISE TRERAPT)

LENGEROVAJ, Alena;-ngggkl-~
The requirements for iwlerance induction in cell-grafts from
adult donors. Folia biol. 9 'no.3:189-195 163.
1. Institute of Forperimenta'l Biology and Genetics, C39choslovak
AcadeiW.pf Sciences, Prague'
. (TRANSPLANTATION) (DOWNIT!r) (CYTOLOGY)
(BONE UMOW) (LIM)

GHAWPA, Miroslav; P_Dj~CKOV.A-PTASINSKA, Marie
Thera-oeutic exercise after gynecological operations. Cesk.gyn.
26[401 no.1/2:97-99 1P 161.
1. 111. porodnicke a gynekologicke oddeleni v Brne, prednosta doe.
MUDr. Antonin Cernoch.
(GYBECOLOGY surgery)
(EXERCISE TEMPT)
V ,

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uxytm from the "n. eirctrolysis Is recommended.
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, IVA I. LFIC I It
P(4,Z A CS1
XOPFUSTIrS, Arno, dr.; POLAOSI, Valeria, dr.
Correct position of perineal region in radiotherapy. Xag7. radiol.
6 no.2:85-87 Apr 54.
1. Foy. Utooki-utcai korhas (Igasgato.- Farkas I&roly, dr., as
orvostudomanyok kwAidatusa) Rontgon-osztalyanak (foorvos: 11oppenstain
Arno dre as orvostudozarqok kaniidatusa) kozlemezWe.
(MIMUM, neoplasms
radiother.. correct position)
(MroTEMRA", in various die.
cancer of perineal region, correct position)

POLACK, Valeria, dr.
lca~~rc~-i~old of the duodenal bulb. Mau. radiol. 7 no.4:
P.52-254 Oct 55.
1. Fovarod Uzsoki utcal korbaz (igazgeto: Farkas, Karoly dr..
ay orvostudomanyok kandidatuan) Rontgenoaztalyanak (foorvos:
Koppenstein. Erno, dr., az orvostudomanyok kandidatusa)
kozlemenye.
(DUODIWIA, neoplasms
argentaffinoma. of duodenal bulb. ding. & incidence.)
(ARGENTAFFINOMA
duodenal bulb, ding. & incidence.)

POLACK, Valeria,, dr.
Gastro-jujuno-colic fistula. Magy. radiol. 14 no.2.*88-91 Mr 162.
1. Fovarosi Uzooki utcai Korhaz (igazgato: Ssanto Sandor dr.) Rontgen
Osztalyanak (fooryos: Koppenstein Brno dr.) kozlemenye.
(GASTRIC FISTULA radiog)
(INTESTINAL FISTULA radiog)

e, Isotopic e Mhar Crystalline
e ji! 9 between
.11j;tBre and Saseous bromine. 1. N-refl. H
P 0 L -:, ,", , .
and A. 11olacrek ( Ingelloninu Univ
Gnm.~, -V-W~m Maryj.-Anc-
extent of isotepic vxchao.-c of Br atorns bttivcca cryst
-OHN -.L, studied by tiugc~ of mdi(mcLh,j
Iigtllrt and 91LSC Dr N%
tmem. Pptd. Hg2Drj contg. radimactive Br couid. by the
Szilard-Oinhurs melhod it-us hicated to varioas teniw. tip
to Igo* In art atm. of I act SBr for 1;5 lirs. 20-
lr~ln 1"olid to giLtMIS
30% of radiNtlitive Br pa
The isotopic, exchange truji not appreciably (dTcctc I by lemp.;
this hillit-acd that tile CKVItange-, nialuiy occurred on t1w 1
Mirfacc of tile Ocample. Sylvia Nowinslut

'MiPhysical Chemistry. Radionhemistry. Isotopes. D-7
POI,
Abs Jour: Ref Zhur-Xhim., No 13, 1958, 4g47o.
Author : Zlotowski Ignacy, Halpern Aleksander, Polaczek
Andrzej
Inst --jagle+1onski University.
Title Production of Radioactive Preparations Enriched by
the Method of Szilard and Chalmers. I. Production
of Radioactive Preparations of Iodine and Dronine.
Orig Pub: Zesz. nauk. Uniw. Jagiellonskiego. Mat., fiz., cheri.,
1955, No 1, ~5-81.
Abstract: The possibility has been ascertained of producing
radioactive preparations of Dr and I having an
absolute activity of 0-3-0.5 AA -Curie by means of
a small Ra-De-source in accoiciance with (n,d' )
reaction. The source having an activity of about
Card 2
12

ZLOTCWSYxI, 1--nacy; YICLACZrY, Andrzej
Kinetic studies of iodine exchange bctween ~,Idrcgen, iodine and
crystalline aluminum iodide labelled with I. Nuk-lecnika 6 nr-. 5:
335-355. 161
1. Warsaw University, Warszawa, Department of Nuclear Chemistry.

P-OLACZEK,_Andreze'; HALPFRN, Aleksander
The effect of electron dnnor-q an the isotap-ic uchange between
aluminum (III), gallium (111), and-Indium (III) iodideja and
alkyl iodides. Nukleanika 8 no.io:667-6 1 163.
67
1. Department of Nuclear Chemistry, University, Warsaw (for
Polaczek). 2. Departm-nt of Radiochemistry, Institute of
Nuclear Research, Wartaw 9 (for Halpern).

ZLOT014SKI, Ignacy; POLACZEK, Andrzej; WINCEI, Henryk
A study of the iodine exchange between KAII4 and alkyl halides E7 the
method of isotopic tracers. Nukleonika 6 no. 6:415-422. 161
1. Uniwersytet Warazawski, Warszawa, Katedra Chemii Jadrcwej.

T,,, 1C I LE N ., J a cek , rgr 1. n z . , ~-- (i I A(, 4"'-L:Y, , " ze 5 law , J* iz ~ ; G0,HAi j Le ,i z6k
MorjGrn measuring techri~-jur - ani 'A..- min'.ng
;A: -.:- ~, - e =
and gas dopo.91ttv., Naftn ~] no..3:72-7i. 1,1.r 16 -, .
I. Pe trole -um Inst-*, tute, Yrakow.

ACC NRI AP603170~" (N) SOURCE CODE: PO/0099/66/040/OC)3/0495/049d
AUTHOR: Polaczek, Jerzy; Pielichowski, Jan
ORG: Institute of Heavy Organic Synthesis, Blachownia Slaska (Instytut Ciezkiej
Syntezy Organicznej)
TTrLE: Bromination of 9-vinylearbazole Lth a bromate - bromide solution
SOURCE: Roczniki chemii-annales societatis chimicae polonorum, v. 40, no. 3, 1966p
495-498
TOPIC TAGS: bromination vinyl compound
:hat
ABSTRACT: It was found
the bromine number of 9-vinylearbazole determined by
the bromate-bromide solution bromination method is three times as high as the
theoretical value assuming that bromine adds to the vinyl group. This bromination
reaction in the dark is one Of substitution rather than addition. Orig. art. has:
,2 figures and 3 tables. [Orig. art. in German] EJFRS: 36,0021
SUB CODE: 07 SUMM DATE: OlFeb65 / ORIG REF: 002 SOV REF.- 002
OTH*REF: 004
Card

FRACZEK, Karimiers; LEPICHi Teresa; PCLACZEKO Jerzy
~~Ill
Ctmarone-indene resins. Pt.l. Koks 8 no-3:94-100 MY4616`3.
1. Insty-tut Ciezkiej Syntezy Orgatdcznej, Wkrszawa.
\1

Lucyne; Andrzej
.... .... . I , - - -
i~ m-rthcd for tle detormination of spartelne beta-camphos-JAIcnate.
Ixta -lol.. phrirm. 21 no.lsl9-22 t64.
1. Z Zakladu t-m-lit-yomega Inistytutu Parmacautyemego w Warazawle
(Kierovnik- mgr W. Dmowska).

POLACZEK,,,-.,Lucyna; GRZESZKIEWICZ, Andrzej
New method of determining E -caprolactam. Chem anal 8 no.6:
961-964 163.
1. Department of Analytical Chemistry, Pharmaceutical Institute,
Warsaw.

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POLACZEK-KOJU-IECKI, Tadeusz; POLACZEK-KORNECKA, Barbara; ZELAZNY, TadcuBs
Bronchoscopy and the bacterial flora of the trachea and
bronchial tree. Pol. tyg. lek. 19 no.3-.89-91 20 Ja164
1. Z III Kliniki Chirurgicznej M w Krakowie (kierownik: prof.
dr. Jerzy Jasienski (deceased)) ; z Oddzialu Chirurgii Klatiki
Piersiowej MSS w Krakowie (ordynator: dr. med. Michal Juszczynski)
i m Pracowni Bakteriologicznej-analitychnej ICS (kierownik:
dr. Janusz-.Rapczewski).

POLACZEK-KOR14ECKI.. Tadeusz-; POLACZEK-KMECKA, Barbara; ZELA-ZNY, Tadeuss
Bronchoscopy and the bacterial flora of the trachea and
bronchial tree. Pol. tyg. lek. 19 no.3:89-91 20 Ja.164
1. Z III niniki Chirurgleme . AM w Krakowie (kierownik: prof.
dr. Jerzy Jasienski [deceasedi) ; z Oddzialu Chirurgii Klatiki
Piersiowej NSS w Krakowie (ordynator: dr. med. Michal Juszczynski)
i m Pracowni Bakteriologicznej-analitychnej MSS (kierownik:
dr. Janusz-,Rapczewski).

i
I
pOLACZEK-Ko~.ECKJ, Tadeusm; ZELAZNYp Tadeuss.
Preliminary observations on the use of neuroleptoanalges-ia.
Pol. tyg. lek. 18 no.45:1683-1681 4 F'63-
1. Z III Kliniki. Ghirurgicznej AM v Krakowlm; kierownik prof.
dr. med. Jerzy Jasienski.

POLAGZEN-KORNECKI, TeLdeuss; ZELAZNY, Tadeuss
- 77
"'- = in- cardiac ostbeterization. Pol. tyg. lek. 18 no
e,q hesia .50:
n
1890-1891 9 Dt63
1. Z III KLiniki Chirurg-*cmej AM w Krakowie; kierownik: prof.
dr. med. Jerzy Jasienski [deceased].

POLLCM-KOMMI. Tadeusz
Bronchoscopy and bronchography with the application of ahort-
acting musc14 relaxants. Polski przegl.chlr. 32 no.7:429-631
ii o6o.
1. Z Oddsialu Chirurgil Klatki Pierslowej MoSPS. v Krakowis
Ordynator: dr W.Laazczak
(BRONCHOSCOPT)
(BRONCHI radiography)
(MUSCLZ MW TS ther)

POLAGUIC-NOMWKI, Tadeuez
t.'Bahavior of venous pressure during pulmonary resection. Polski
przogl. chir. 32 no.12221,95-1199 160.
1. Z III 33iniki Chirurgicznej A.M. v Krakowie Kisrownik: prof.
dr T. Jasienski. Z., Oddzialu Ghir. Klatki Fiersiowej M. S. S). w
Krakowie Ordynator: dr W. Laazczak.
(PNMONECTOMY) (BLOOD PRESSURE)

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FOLkGj7EK-K(;Rll,ECKl . Tade-usz; 11:1SS , Jolui-Aa
Prognontic value of p~,rllph,~rul ven,~-,ls presoure in c lon4c~u '-Lrrw~lc
injuries. Pol. t:,19- 16-k. 19 no-13:471-473 23 Mr '64.
1. Z III Kliniki Chirurgicmej Akademii lMe,'vcznej w Krakovie
(kierownik: prof. dr. ined. Jerzy dasienrIA-1 [deceased]).

POLAGZM-NORNECKI, Tadousz; POCHOPIMI, Franciszek; WOJCIK, Emilia
Treatment of the localized inflammation of the bronchial mucosa
in the course of the lymph node pulmonary tuberculosis. Gruzlica
33 no.9,.779--183 S 1 65.
1. ZOddzialu Gruzlicy Plue i Dzieci Miejskiego Szpitala Spee-
jalistycznego v Krakovie (Ordynators dr. mod. F. Pochopien) i z
Oddzialu Anestezjologicznego III niniki Chirurgicznej M v
Krakowie (Kierownik Klinikit doe. dr. M. Politowski).

POLACZEK-KOUINVU, Tadpii~--z; KR'7Y,,)TE(-W
Anesthesia in igurgery of the extra"bulb&r ocular muscles. Klin.
oczna 35 no.2:309-313 165.
1. Z' Oddzialu Leczeiii.a &za w We*aw. Dzieciecyri Szpitalii
Okulistyemy w Witkowicach (Cli,ynator: dr. med.
K. Yrzystkowa; Konsultwnt naukowy: prof. dr. med. M. Wilcz&-)
i z Oddzialu Anestezjologiczpego III Kliniki Chirurgicznej
Akademil Med3rCznej w Krakoide (Kierownik kliniki: doe. dr.
med. M. Politowski).

POLACZKOWA, A. : ACHMATOWICZ, 0. : BOHM, J.
3-4-5triphonylbenzoic acid.
P. 115 (Rocz niki Chemii) Vol. 31, Nol 1, 1957,, Warszawa, Poland.
SO: MONTHLY 1NDEX OF EAST EUROPEAN ACCESSIO14S (EEAI) LC. VOL- 7p NO- 1, JAN. 1958

POIAM/E~ectricity - Semiconductors. G
Abs Jour : Ref Zhur Fizika, No 4, 196o, gogi
Author : Deren J., Polaczkova, E.
Inst :
Title : Investigations of the Electronic Properties of Tungsten
Trioxide., I. 'The Electric Conductivilty of Tungsten
Trioxide Within the 1000 -- 7000 C Temperature Range.
Orig Pub : BuLl. Acad. polon. sci. Ser. sci. chim., geol. et
georgr., 1959, 7, No 5, 313-320
Abstract : Investigations are made of the electric conductivity of
W03 on the temperatvre in the interval 100 -- 7000 C.
It was found that J.D. all the InvestigELted intervals, the
electric conductivity cannot be expressed by the equation
exn (OB/T). There exists a limit (below 3500
C) when as the temperaturc, increases, a- reaches first
a mximum, then a minimun, after -which a further increase
occurs. The investiVAtion of many factors (composition
Card 1/2

DEREN9 J.; POLAGZKOWA, E.
Investigations-on the electronic properties of tungsten trioxide.
Pt. 4. Bul chim PAN 12 no. 3:189-196 164.
I.-Department of Surface Phqnomena, Institute of Physical
Chemistry., Polish Academy of Sciences, Krakowt and Departne nt of
Inorganic Chemistry, School of Mining and Metallurgy, Krakow.
Presented by B.Kamienski.

DEREN, J.; POLACZKOWA, E.
Investigations an the electronic properties of tungsten trioxide.
I. The electric conductivity Qf tungsten triaxide within the 101?.
700 C temperature rangee IL Current ves voltage characteristics
of tungsten trioxide within the lOe-700*C temperature range. III.
The influence of surface processes on the electric conductivity of
WID3. Bal Ac Pal chim 7 no-5:313-332 159. (EW 9:9)
1, Laboratory of Surface Phenomena (Craoow)p Institute of Physical
Chemistry, Polish*ademy of Sciences and Deparbient of Inorganic
Chemistry, School'of Mining and Metallurgy, Cracow. Presented by
B.1anienski.
(Tungife-n oxides) (Electric conductivity)

POIACZKOWA, Ewa, dr
- -~' -T~'
. -, -
Influence of chemisorption of vases on the electric
0
conductivi.ty of polycrystalline specimens of tungsten
trioxide. Wiad chem 18 no. 2: 123-128 F 164.
1. Katedra Chemli Ni(oiganicuiej, Akademia Gorniezo-
Hutnicza, Krakow.

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*Introduction to the electronic theory of organic compoundsO
by G, laragounioe Reviewed by W,, Polaoskowa, Wiad chem 15
no.llt736-737 N 16i.

1
,:..- POLll=OWAL.Wj._
"- i,
I . -1 ~.
uOrganic chomistryg by Louis P. Fieser, Mary Fieser. 2d ed.
Reviewed by If, Paia*owa, Viad chem 16 no&12:779-780 D 162,

1.; 41810-66 BRI I jwAr
ACE ___ I* -~'AP&jiZ94 (N) SOURCE CODE: PO/0099/66/040/003/0421/04281
AUTHOR: Czerwinska-Fejgin, Eugenia; Polaczkoway Wanda 20:
ORG: Department of Organic Chemistr7, Institute of Technology, Warsaw (Katedra
Chemii Organiczrwj Pblitechniki)
TITIE: 4W-disubstituted o-terphen3r1jerivatives
SOURCE: Roczniki chemii-wmales societatis chimicae polonorump v.' 40, no- 3, 1966P
421-428
70PIC TAGS: noi tallic organic derivatives organic ead compourod
ABSTRACT: 1-phenyl-2-(p-phonyl)hexam-195-diones were cyc3ized to 3-phenyl-4-
(p-X-phenyl)cyclohwwne-2-onee (X - "q CNI, Clp OCHjs OH). The oximee of the
latter were armatized to-the corresponding 49-amino-4-X-o-terphenyls. Orig.
art. has: 3 tables. [Based'on authors' Eng., abst-61 IJPRS:- 36,0021
SUB CODE: 07 SUBM DATE: 29Jun65 ORIG REF 1 001 OTH REF: 003

10 811 Ewp(j) ---JW/RM
N) SOURCE CODE:
AUMOR: Caerw1wks-FeJain. 9- L Polacskuwa, W.
ORM Departiesisst, of Orgaide Chemistr7m Institute of Technoloug Warsaw (Katedra
chanii Oramicartej Politechdki)
TrMs ConjusatioJin the o-te system
is-w-wMi
SODRCZI locani1d chadi-mmales societatis chimicas polonormlo ve 40# *noe .3p 1966P
429-435
TOPIC TAGS: UT spatrum, nomtallic organic derivative
ABSTRACTS The trasimmission of the substituent effects in 4.4 '-disubstituted dipherW1
amd o-ter"wrW1 derivatives was compared by wasuring the ultraviolet absorption-
spectrae Grige arts bass 3 tables* Named an authors' BM* abat.] 1JPRS: 36POO21
SO COMs 07 / SM DkTls 29AFr65 / MIG MWI 002 / SM MI OM
MH WWI an
eAMA 11 A &f

POLACZKOWA, W.
"Principles of organic chemistry" by A.Cziezibabin. Reviewed
by W.Polaczkowa. Wiad chem 16 no.1:60-62 Ja 162.

POIACZK.q~~A,__~a~a; FOROWSKA, Natalia; DYBOWSKA, Barbara
Studies on the influence of phenyl substituents in the
benzene ring upon the not neighboringfunctional group. Rocz
chemii 36 no.1:41-50 162.
1. Department of Organic Chemistry, Institute of Technology,, Warsaw
Laboratory No-4,, Institute of Organic Synthesis, Polish Academy
of Sciences, Warsaw.

Polaczkowa W.
Polaczkowa W. "3-Indol-Butyric Acid." (Kwas 3-indoillomaslowy). Przemys
Chemicz , No. 6, 1950, pp. 340-343.
In order to secure a higher yield and degree of purity - certain modifications
were introduced into Jackson and Manske's method of 3-indol-butyric acid preparation.
The reaction of obtaining phemylhydrazone deritative of an acidic ester of 2-ketopiM6
ic acid from cyclohexancne-2-carboxylate and benzene diazonium chloride,--was carried
out in a dilute alkaline solution, without excess of KOH, and resulted in producting
phenyl-hydrazone of 94% yield without pigment admixture. The decarboxylation process
of indol-2-carboxy-3-butyric acid was performed under diminished pressure (about 30
mm). The conditions described make possible production of 3-indol-butyric acid from
cyclohexanene reaches 22% of the theoretical amount.
SO: Polish Technical Abstracts No. 21 1951

Ac_- h
L
I I"ll.lich mmicit 0., 111;.,Iit ;vmc
I. "wivill, o it It m .... 1-11*,., tditil'.1 11), rivill: I".111:1w -A I"
Willu, (I I Iold 0 6. Wit It I Ill! foll.w. ill'i d, imI-
I d. wit Nor i, 1, lo, ol I" felt .,ph. w I.
t IV 't-
I I id. 4-,;11.-. if I I it,- -I i I at-'l I I %.I ~, t I I; It.II1v j, it i It I
be, I Z, Illi I It I-, Ill, I) I it it ni I I i1r. and 'ovi I; d r %-It m, 4. 1 do(
it,,( It,im ith acvlolliflilv pli'l 0-folliltitlih. (!u-rir Ism.
(iwl bl~jwvvll I aild 11 ;~ i"Ilic. Th, I .... m
ilratwv). 1. r a ea,-
Iliv mul. tt-irfitt, increa,,-4 w-gative fli:-ts fut tit flit! mi-
ni'le N atmil, tit(- gwawi till. mte or I-o-.I;.,ZI. fill. ii-mrs.
lion Lor 1.11 iInlic Complex ill tilt- firA '111,.i~ "1 #11, lem-flon iq
lluj~llll 11%ltlif!tliwll:lti"iiof:tr).Iir OfcIccttImI0!;- Ow N oloill tit
fit, to, tile dii-lic.
--tollillitlile IwId -17 Ill. at L`,4 give It
-rdilorate (V). lit. ~q- 279.5'. 2-
I and /-lne 01'ayl't-lizo-
Ili rile :0 lie, lit give 70.3% vichl, li't. 104-
195"; V, no, 287-2WO,
I will /A-ronn-Amizirmitifle livate(I if I lie!;. lot 230 -2,`41'
Five 861,,0, tit. '_15iI,-2F,7*.
dine. I ai-rd m-bromobenzonittile lot fl~i IIXI lit,
givi: 62.3%. )-ithli m.
diric, I nuirl lperim)-i cyanifle fit 250-270"' five 1:1 lir:;. ive
F
49,61/0, in. V in 241-2-12'. All III orr cry
wwk lowwcf;: (tic 0111V iN ('11ey Vivo mt! V. The riffillors
Itiol tilt.. fullowing, flicite till - uw-_-.sflf1
trite, rind pbertraithirctic, plicnazinc. %vidi malcic unlipfridt-,
et hyland i~oanjyl cyanoformat P., berizontitrile, natmti I rile, d i-
aMtrillilicibenzene. or tire roxime will ketimiric of brimn-
Illicitoric with 2,3-diniethyl bufadictic. bew- nnd toln-
antlitaccric r.
fitrile urith IV was cobtairic fiction
of I (Zn tltt,.t I IICI) wid Fives, by crxidwt (KANO.),
MaCO)s.2 Tuvk-.-: of HiC0,11. A~ .-I~rsf-v

jetrseCnL1CYJ0DPMt2dl?noT1e with
Men "U11003
miry); cf. C.A. 48, i135%-,--- Tara-
(lf)53X'Q,-,nch tAnnioxe (1) irracla jrueb faster (fo-W inin.)
irr
P
'>:1C7xJl0 tadirx -Mroe"14COC'V (]-q) than with
Uith B.-Cira(D) 'Of -Itil
,,,math altU" (30~ M brx.). The Products, 2-Un:0Y'_
yidias (IV) und
(y). form free g-adical, in the
3A.5104dra nyj
t1n. ,d wt easily reduced to the cerre
by b) CLMY515 Cd P-
Speoniding carbIncls. 11 WAS 'nblalocd by conder=tiun cf
J.".YCAIV: Ct CJV)PA P"Od. VI (125 Z.) and 150
PbCHICN and P-Mft*';CT.1W0 (M). to,50"Shal-en until
S. CMcd. H3S06 in U5rals water lituttil ~d with NaHCOi'and
.11 VI dissolved, extd. with CA, Wash'
ad distd. gave 40 1. (81%) 11. b. 2OS-10-
%vitb wata, dried- x - EtOH and
,rly, 29 g. p__M.0C.H,CHjC,14 in 2DD jnl
S,.,L
ltb 2 roll. 33% Na0H,
So Z, VIE Imted to WHAR, MAIV4 w ~~ red crystal I Of P-
r,auxed for 2o -In and cooled g&%
'a
.Ar"NC.H.'V: C(CN) OM, (M), ra. 154.&-5.6* (from
alt.) (yield 23a 50 S _de VIII gave on by-
.NC~H,CH.CN
drolys13 28-8 9-
and 7,15 9- Vn In 10D mt- ale, and 0'5 ml' 33%
-MC2NC4H4N: C(VN)C4.H#No'-
0.1 K. (62%) p .-
(slightly dec=P~
(lx), violet crystals IrDru ale- m- 18G-1
51 S. 3X n WD Q. C.14 and 9D g. 50% jjS0, shaken
t fiDo %Mtn the red color, changed to YCP-,
a walled with NalIC03 "d witil water,
t h ~ Milly y
c-cmird. 10 10 WIL, nua mired wl!b 50 ML PW- eL%C-' Save
AjVCjj'Cj)CjY'M'1I4-16'. IOUs.)
yellow crYstab Of
and 9 4.33 UTre t led to MI fcr I br. In dry Atim dis-
el E;T
.Aved In 150 MI. C&Hl. gmd 2bAcD twi;-"- with 40 mi. P
tic.ns at 5% Na0H I- -tral Jim. The C.H. luye: contd-
I tall. 710% HCl0#
t, so tri, and ask= IDT 04 hr- wlLh 0
VI)
L wq
P-art D 'I nidg 1 Of' 4it'g-ri'119Y., aiu.rlZM-si7i'in(g1rnthme -
-AcCill); IV-1109i drml;)). M -m;ily hydrWymi to IV.
1113.2g.)Uari 11.19. ill hc.J-4 as di,,wlvrd ia 75 mi.
Cilh, tmd ghaken Willi 15 m!. 70% 1100, c-svc,% rpt, w~kh,
zsb--J with Cilia, r-tr- t1her, ii~d -aftl, E;iQ!CA7e-d En
AL011 and epptd xuh water Yielded 10.1 g. 214
Ili* (from 1 9. IV refluxtil in dry ntm, with 7 mi.
35% K01I in dry RtO)l until completcly di5W1lVCd. diluted
with water. and extd. with Et,O gave zdtcx di3tti. of Ht,0 -
tin almost quant. yield of p)iray1-Z-(3,4,J,6-1ejra t hrxYipyri.
dy1kcrbixo1(X), tn. 182-3' (from ale.)- 1100. so , d--comp.
above 150*. Similarly, V gave 4-me;J'.--yPh,..W-2-(3,4,5,6-
wrath:r%yM1-,ridy1)ca?bi?j&1 (XI), m. 17fl-7' (from MtOH or
RtOH); A jall, decomp. above 150". Almost quant.
Acids of the carbiriols weTe allo obtained when the ket-mes
(0-1 g.) were reduced with I 1. 2% X arnalsem in 8 mt. dry
PhMe, 2 ML dry HtsO, and I drop abs. EtOH in a glas3-
stoppered fliak; 0.1 q. IV db2olvid In L2 ml. dry PhMe
dduted with 12 mi. dry EL30 and treated with 0-016 g. K
in an atm. of dry N ga7a a deep green free radical soln.
which, alter 3 days was detolorizzill instandy by addii. of 2
mLEWHanddistd. Ile residue washed with dil. HCI and
wilb water, dried (m. 172- W), and taken up with Et2O
rive 0.04 g. IV (hisol. in RtM and 0.02 g. X (&at. in EtO).
Similarly, 0.1 S. V with 0.44 g. K amalgam gave a green
-in which yielded a mixt. of V ard )[1. N and V gave
grec;' free mdic2i solos. with No but the reaction was can-
siderably 5!ower than with K. Tetmphenylpyridine drrivs.
(1.5 X.) in 30 ml. AcOH be-ated to boiling with 5 nil. 70%
TIC104 gave PtrChlXateg (recry5td. from AcOll); 2-(p-
M. 302-0*
(decompri.), Wt at
- c
m 311 14" n dark at
',U5*; 2-(P-??.ciloi7p.hisyl)-3,4,5,6-teirap enyjpyr ise.-
ij
HCV., m. Z~3% (decompn.), soft and diwk at 1W.
The compd . m. ~31-2*, previously reporied as the per-
clilwate t.4 N was farad to be the fr"~ b m_

PQLACZKOI-4.0, W,; BANKOWSKA, Z.
-E~
"Chlorination of acetone. Obtaining of 1, 1, 3-trichloroacetone.11
P. 119 (Roczniki Chemii) Vol. 30, no. 1, 1956
Warsaw, Poland
SO: Monthly Index of East European Accessions (EEAI) LC. Vol. 7, no. 4,
April 1958

POLAND / Organic Chemistry* Synthetic Organic G-2
Chemistry*
Abs Jour: Ref Zhur-Khimiyaj 1958, No 17# 57394-
Author :,Eolaczkowa We# Achmatovicz Oaq Bohm J*
v
Inst :NO g vene
Title :3,4p5-Triphenylbenzoic Acid.
Orig Pub: Roazn, chemes 1957v 41p No lp 115-122.
Abstract: Synthesis of 3.4,5-triphenylbenzoic acid (I) is
presented for the purpose of determining Its
structure. The starting materials employed were:
4-oxi-2,3,4-triphenyleyelopentene-2-OH-1 (H) and
anhydride of maleic acid (III)p which at a molal
ratio of MI11 = 1:1 in the diene synthesis form
Card 1/6

POLAND / Organic Chemistry! Synthetic Organic G-2
Chemistry.
Abs Jours. Ref Zhur-Xhimiyas 1958, No 17, 57394-
Abstract: forms V;~ than as the result of aromatization and
of splitting-off III transforrm into I; VII is
produced from V as a aide reaction. 32&,6 gr of
II and 3902 gr 6f III are slowly heated up to
200-2100j, after 30 minutes the mixture is cooled,
CH OH is then added,, and filtrated. A yield of
631 V of 315-3170 melting point is obtained. VI
is obtained by dissolving V in 2% NaOH solution
and by precipitation with $% aqueous Hol. VI is
cogverted back to V at as low a temperature as
90 . The methyl ester of VI having 216-2170
melting point is obtained from VI and CH2N2* IV
Card 3/6

POLAND / Organic Chemistrys Synthetic Organic G-2
Chemistry*
Abs Jour: Ref Zhur-Khimiyas 1958P No 17, 57394.
Abstract: dueed into the apparatus. 10 gr of V and 3.5 gr
NAOH are dissolved in 50 cc of water, neutralized
until pH of 7 is reached, and then precipitated
,with CuC12'water solution; the obtained 13.58 gr
of light blue powder is then treated.with 50 cc of
quinoline, heated at 200.0 for 20 minutes$ 5 gr NaOH
in 50 cc of water Is added after oooling$ followed
by the removal of solvent by steam stripping. The
remainder is recrystallized from a water solution
followed by dissolving the obtained crystals and
by precipitating with HC1. A yield of 46% of is
having 265-266.50 melting point (from alcohol) is
Card 5/6

C-,;,
P '49
0'.
jk Cl
, .

7Z

1

-
Dist c.--- C. '2
3,
! d/ 4 E2 c
4E
. I
and WO bm, =r 2nd. 70 h.-3., rcap., Ltk!
'
'
hit, m. 145-7
, or Et ester, m. 111-12
. f;! 3,M-trioh)Dr~
uiu. 'With M.-ONa the-!-c emrs form
the tamt Ife cs*.tr of
piroliric acId (1), m. 107-0, whisch cm =M hydr-lysip
1l
d
awi
).
t

dmcwp. 2N' wft~. 0. M atld I" 'flon
of
Chbro-&bmzoyl~i ulinr, .. 2N.-S'. Alk. hydrolr-is of
I leads to the cwnsponding methaxy acid, decimp. 200%
which ou --nelfing updorgon decwbixylation to 3,&41i-
chloio-d-metho~ty-6-benroylp,,,,rid-,-it, a,. 184-5.51.

Aj D A 2- K
Distrt Wd/IiMc(J)
;~-iierlvatlvez of M Lrol
a
kowsli, Danutil Kliniczuk-Sown, and W
l
aWT
. "' "I
-S
b
i
i
h
l
l 5
d 1
2
3
-tr
- ute
evera
su
st
t
summary).
cay
,
.
p
511
"i
I . derivs. (1) were obtained and the reactivity
1
of their functional groups compared with that of 4-substf~
tuted N henyl derivs. The small differences In reactivity
observffm several cases may follow not only from more
restrained conjugation in I than in the biphenyl system,
but also from both conjugation and inductive effects super-
imposed on each other. The synthesis of I was based on
condensation of benzoin with btnzylidrneacetone and on
-aromatization of the 4-hydroxy-3.4.5-triphenyt-2-cyclo-
hexen-l-one obtained, 3.4,&Triphenylphenol (11) (Me
'
0
ether, M. 122.5-3.6
; Et ether, m. 110-11
) witla PC4
guveS.4.5-Pii,C~HICI.m..43-4*. The same Cf coinpd. (to-
2-di-Cl cfjmpd
ether with 1
) was obtained from Smitb's

.
,
etone (cf. Chem. Bcr. 26, 05 (1893)) directly. 3.4,6,-Phl-
f
C.1i CN was hydrly.~d to the acid; chloride, m. 131-2*;
'
00
-l
amide, m. 2
. A. Krqglewskti-.-

4

K
_zz-

/Merhan'sm of the reaction of I'lethl ~b-Mocinnamate
jadwiga Urjes and Wanda Folamkowa
with bydrazine. I an
(Politechnikai Wa_m__w-T7-7wzniki i
surnmary).=In the study of action of NIH4
9
9l
W
'
P
;
under various condi-
.
S
'C4114CH:CHMMe (H)
I)
p
tions, p-BrC~H,CH:CHCONHNHj, A-hydrazino-p-bromG-
h
dr -i andAp,~bro heny'"

t1d..e that IV
V . (IV t It ggt7
;
formed from IU or from (nonisolated) Me P-hydrazino-/~
bromohydrocinnamate, depending on. reaction. conditions.
The reaction of I with 11 runs in two independent ways:
by substitution it the carbonyl (hydrazindlysis) and addn.
to the ethylenic bond. The bydrazino -ester undergoes
further substitution at the carbonyl group. Depending on
I co
ncn., this ester reacts with I or undergoes intramol.
'
cyclization. Cyclization of the hydmzi e is much slower
than that of the ester.. Water reduces the hydmzinolysis~
rate and inhibits the tramol. more than the latermol. re-
action. A. Kllqgleq*~-)
4"1 Distr: 4E2c~j)/4E3d

POLAND/Organic Chemistry. Synthetic Organic Chemistry. G
Abs Jour: Ref Zhur.Khiri.p no 2, 1959, 4656.
Author Czervinska-Fejgin, E.L kova,11., and
Sokolowska, A.
Inst
Title on 3s4I5-Ti-ipheny1wdline-
Orig Pub., Roczniki Chem, 32, No 2, 265-970 (1958) (in Polish with
rM9318h and Russian Surmaries)
Title The rearrangenent or the oxine of 3,4,5-tiiphenyl-
cyclohexene-2-one (1, la oxime) under the action
of (CH4CO)~O (II) and of CHSCOC1 (M) in the
presence of pyridine has been used in the synthe-
,ZNH-COCHj (IV). The hydro-
sis of 304,5-04R~r~', 94H
lysis of iv gives 4,5-(CjHst06HZNIk M- The
Card 1/4

POLIM/Organic Chemistry. Synthetic Organic Chemistry. G
Abe Jour: Ref Zhur"Xhin., No 2, 1959, 4656.
CHsCOOJI are added over 30 min at ^/ 100 to 0,54
gm NaNO4 in 3.8 ml cone HASO~; heating for 50 min
at 1v 100 0 followed by standing for N 12 hra
gives 41,,4~ vi, r3p -224-226 0 (after distillation at
210-2150/15m; from CHICOOH). The diazonium salt
solution prepared in a sinilar manner is added to
1.23 ga Cu4ClL in 3.5 ml cone HC1, the solution
is heated for 15 min at rv 1001, the residue is
distilled at 16o-170'/15m, distilled in ether,
washed with XOH and with CHjOH; the ether solu-
tion yLelds VII, yield 30q/, mp 138-1411- --
V. Skorodumov.
Card 4/4
19

COUNTRY
CATEGORY
ABS. JOUR-
AUTHOR
_r
: Polaxid
: Organic Chemistry--Theoretical organic chemistry.
: RZKhIm-, NO- 22 1959, 1;0' 784971
: Dole*, J. and Polae2kown, W._
: Ko~ given
: On the Mechanism of the Reaction of the Methyl
Enter of p-Bromocinnamic Acid with Hydrazine
ORIG. PUB. : Rocxniki Chea,.32, No 6, 1243'-1255 (1958)
ABSTRACT : Tho - reaction of K2 H* - 14 0 (1) with 4-brC6 06 CHuCH000.
CH3 (II)s d*P6AdiUg CA the canditione used, gives j
4-DrC~IkUnQHCOW014 (-&!I), 4-BrC6H4CH1%N11NHj)CH2_
WNW% (IV), 5-(p-brosophonyl)-pyrazblidone-3 (V),
and (4-BrC6114 CH=CHCONH2 ) Ceic3 (VI), Apparantly
V is formed from IV oT from 4-iirC6 HN CH(NHNN2 ) CH2 -
COOCH5 (VII) which has not bean isolated and the
hydrazinolysis of which proceeds markedly more
readily than that of 11. Depending on the con-
centration of 1, the Intermediate reacts either
CARD: 1/10

0 U T RY Pol and
CA T Z G 0 RY
ABS, JOUR. 22 19~:D,
Cirl
A B`J~ T RA 0 T t 10 n 0 f V I I I v., -L t h C H,? N? o r C; i4 0 H gi v e -s -p
87-890. About 0.0~!5 mol I! and 0.0"15 mol- of
IOU% 1 in 10 ml C14)OH are rt-r!.uxed for 15 ma,
6vaporated ovar 1~-,~04 to drynez;u, ond the rrm--;~Ne
is rins!!d wltii ttherl the y1eld of IN it,
mp 81.5-15' (decomp; frnm alcollol), d.J.acetyl ie-
rivative (DAP) mP 234-2350 (from aqueo-.;s a1c).
The combined ather extr&ct yieldB 0.2 gm !IT.
mp 163-16(3,53. The same reaction with 2 hr
reflux gives 3 Ems of crud" produf~t which oL
CA2-TI. 3/10

COUNTRY
CAT~MORY
Poland
ABS, J OUR. RZKhim., io. 22 1959t
A 11 TH 0 F,
112.
G-i
784971
0 "1 IG. IDUB
ABSTRAOT and 0.4 9M of an apparent mixture of IV and V.
0-05 mol 11 in 50 ml C-1-IjOH is treated with 0.15
Mol of 20% 1, the volution is allowed to stand
for 4 days at about 20*, after which the fil-
trate is gTadually evaporated In a dessicator,
the precipitate being removed from time to time;
the yield of III is 40.2'%, mp 14.7.5-1690 (from
ale); 1.7% of impure VI and 26.5% of IV, mp 79-
62' (decomp) are also obtained. About 0.01 mol
IIT in 50 ml 'F4 GODH J.E coole'-1 to 5', 0. 01 mol

I, Ou I i T RY Poland
CATEGORZ
ABS. JOUR. iUXh1w., V10- P2 1 0 78497

AUTHOR
t Yj qra

ORICIT. PUB.
ABSTRACT &Lving 35% of unreacted II, 18.8~6 III, and 19%
V; the alcoholic mother liquor on evaporation
of the solvent and acptylation of the residue
gives 0.4 gm of the AP of V, correspending to a
yiela of V of 5.8%. Abo-dt 25 mmol 11 and ?5 mmol
I in for 11- min; frac-
.50 ml CHsOH are refluxed
tional crystallization gives 155~ unreacted !T,
26.69-,. 111, and 28.7i% V. About 25 mmol 11 and
25 mmol I in 7 ml CH3 OR are refluxed for I'll min,
leaving a residue of 2.5 gms of unreacted !I;
CARD: VIO

C, CJUA T R Y Polarld
CAIT Z G, 0 13 Y
ABS. JOUR. iz"Kh.l*..B. A0. 22 19-59, "849?
ORrx. PUB.
ABLSTRACT GICOC)C2 the solution is etirred for 2 hrs at
temperatures from -2 to +2', and 0.03 Mol an-
hydrous 142114 in 50 ml Oil Cl~ is added gradually
to the solution; the precipitate and Lhe reai:lue
remaining after the evaporation of the filtrat.-a
F,iive 25~6 III awi VI Ccicl, mp ~06-tlO' (decc~vr;
from aic). About _~-%. mmol if-i~rf,36 111, C in
20 wl CE501i is treated wlth 0.05 mol I and the
resulting solution is heated for 1 ar at abOut,
evaporated-, the yield cof 3-(p-bror,,ophe_,.jIN
160 and
9/10

JAWORSKI, Tadeusz; POLACZKOWA, Wanda
Diene synthesis of pyridine 1---ing; reactions of tetratChlarocyclopen-
tadienone ketals with benzoyl cyanide. Rocz chemii 34 no-3/4:887-
898 6o. (EW 100)
1. Katedra Chemii Organicznej Politechnikig Warszawa
(Synthesis) (Pyridine) (Tetrachlorocyclopentadienone)
(Acetals) (Phenylglyoxylonitri-le)

D&M, Jadwiga; POLAGZKOWAI Wanda -
On the reaction of bydrazine with ring substituted derivatives of meth7l
cinnamate. Rocz chem-4i,35 no./.,:8/,3-852 161.
1. Department of Organic Chemistry, Institute of Technology, Warsaw.

DELES, Jadwiga; POLACZKOWA, Wanda
On the mechanism of the reaction of bydrazine with cinnamic acids
asters. II. Rocz chemii 35 no-4:853-M 161.
1. Department of Organic Chemistry, Institute of Technology, Warsaw.

POLACZK , W
~-----OWA Mjdj,,- POROWSKA, Natalia; DYBOWSKA, Barbara
The influence of phenyl substituents in the benzene ring an the non-
neighboring functional group. I. Benzoic acid derivatives. Roes chemii
35 no.5:1263--1271 '61. -
1, Department of Organic Ghemistry, Institute of Technology, Warsaw
and Institute of Organic Synthesis, Polish Academy of Sciences, Warsaw.

KNOPF , Marian; P01ACZY , Jerzy. - ~ ~.
Potentiometric studies of zinc paints. Polimery tworz wielk
8 no. 11: 423-426 N 163.
1. Instytut Farb i Lakierow, Gliwice.

BAKULI.. V.N., kand. takhr.. nauk; FOLADKO, Ye.P.., inzh.
Using drill bits of snall and redueed diameters. Met. i
gornorud. prom. no-4$44-45 J1-Ag 163. (MIRA 16:11)
1. Institut averkhtverdykh materialav Gosplana UkrSSR.

POL"nc!7, 'x
Azex-'r.,.ijJzhan SS.R Kend Toserrufat-, 40 -11do. Raky,
Azorneshr, 194
h
181 p. Illus.' Tabl~~S.
Te--d. in Azerl-ailiani
Rusqian Title: STE, IS,UfE I-.T0ZZ-:'A'-,'!T--70
SKC7[ 733J, Za 40 Let.

ponmvj I-tj 14,
Dissertation: 0-7amlysis of Agricultural Technique With Cotton Plants
of Leading Kolkhozes of the Safaraliyevskiy Rayon of the Azerbaydzhan
SSR and Measures for Their Future IWrovement." Cand Agr Sci, kzer-
bWzhan Agricultural Instp 8 Jun 54. Bakinskiy Rabochiy, Baku, 30 May 54.
SO: SUM 2849 26 Nov 1954

POLADOV -kande sellkhoz, nauk., otv. red.; YJiALILOV, A.G.p
prof., red.; RUSTAMOV, S.G., prof., red.; RUSTkMOV,
W.G., red.; YAGHUROVA, T.p red.izd-va; IBRAGIYGVp M.t
tekhn. red..
(Problems of the overall use and conservation of water
resources In-tbe Azerbaijan S.S.R.) Voprosy komplekonogo
ispollzovaniia i okhrawj vodnykh resursov Azerbaidzhan-
skoi. SSR. Baku, Izd-vo AN Azerbaidzb. M. 1963. 462 p.
(MIRA 17t2)
1. Akademiya nauk Azerbaidzhanskoy SSR. Baku. Sovet po
izuehaniyu proizvoditelltqkh sil.

POLADOV. Novoum Musa ogly
(Agriciulture of Azerbaijan during the last" 40 years] Azer-'
baocjam SSFL kend ieserirufaty 40 ilde. B96, Azerbsichan
dov1st neshrilaty, 1960. -p. (in izerbaijanil
(MIRA 14:5)
(Azerbaijan-Agriculture)

ANTONOVSKIYY V.L.; POLADYAN, V.E.
Iodometric and ferrometric determination of cumene peroxide.
Zhur. anal. khim. 19 no.2:248-253 164. (MI-RA 17:9)
1. Novikuybyshevokly filial nauchno-isslodovatellskogo Instituta
sinteticheskikh spirtov i organicheskikh produktov.

WUCHARQV, Aleksandr Bagratovich, doktor sellkhoz. nauk; RASI-ZADE,
Shamil A. ogly; BYSTRITSKIY, Vladimir Yefimovich;
red.3 AKIWDOV, S., tekhn. red.
(Improving the quality of animal husband~7 and developing the
Caucasian Brovn cattle breed in Azarbaijan]Kacheatvennoe uluch-
shenie skotovodstva i sozdanie kavkazakoi buroi porody skota v
Azerbaidzhane. Baku, Aerneshr, ~962. 237 p. (MIRA 16:3)
(Azerbaijan-Cattle *eeding)

USSR/Farm Animals. Cattle Q-2
Abs Jour : Ref Zhur - Biol., No 19, 1958, No 88olq
Author -. Poladzade, Shindyan ;,.
Inst
Title : Dairy Animal Husbandry in the Kolkhozes of NaGorniy Karabakh
Orig Pub : Sots. s.-kh. Azerbaydzhana, 1957, No 6, 34-37
Abstract -. No abstract
Card : 1/1

)?OLAI, Gyargy
Conditions of the Lower.Lias coal deposits in the Komlo coal
basin from the point of view of mining geology. Foldt kozl
93 no.l-.3-14 Ta44r 163.

F-OLAmia,_~.
Ga)GRAPHY & GEOLOGY
POLLMAtR, S. The Kokra Valley. p. 209. Vol. 27/28, 1955/56 (published
1957).
I-Sonthly List of East Earopean Accessions (EEAI) Vol. 11, No. 2.
April 1959 Unclass.

POIAJNARP S.
Medvode,- som geogmphical notes* p. 1.
Periodiml.- CEOMAFM 0BZOHW.
aEoMRHr & MOWGr
Vol* 5. no* 4P 1958e
SO: Montbly List of Eut Europmm Accessions (EEAI) IZ
Vol, 8. No. 4
April 1959, uncl.

POLAK, ALOIS
Slovnik tkanin. Lr-Vyd. 1-_7 Praha, Fru7slove vvdavatelstvij, 1951- 123 P- (Kniznice
textilniho a odevniho pruMslu, sv. 10 LI-A dictionary of textile fabrics. IUus._7
SO: MONTHLY UST OF EAST EUROPEAN ACCESSIONS, LC., VOL. 3, NO. 1, Jan. 1954, Uncl.

POLAK,_~ff9lf-,_~NDr.; STEMPROK, Miroslav, promovany geolog didat geologicko-
mineralogickyeh ved , kan
Use of albitized Ginovec granite as substitute raw material in
the ceramic and glass industries. Geol pruzkum 5 no.8:227-
230 Ag 163.
1. Ustredni ustav geologiclW, Praha.

M
POLAK =, mgr J nz.
-
Petroleum Institute experimental ststion for IrfIlUrg -z*~e,-h,-,'-q7:eSz
Nafta 21 no.4;99-101 Ap ?65.
1. Petroleum Institute, Krakow.

POLAK, Adolf, RNDr.
- - - -------- - - - -- - - -
Forecast reserves of mineral raw materials. Geol pruzkum 6
no.5:129-130 My 164.
1. Commission of Classification of Mineral Deposit Reserves.,
Prague.

POLAK, A.
"Experiences with a mobile falsework propelled by electricity used In the
construction of grain elevators in Hurbanovo and in Vrable."
P. 214 (Stavba) Vol. 4, no. 7, July 1957
Prague, Czechoslovakia
SO: Monthly Index of East European Accessions (EEAI) LC. Vol. 7, no. 4,
April 1958

;'CTLAK~, Ado-Ify RN'Dr,
Cal~:ulatj~~n of resenres and the Cor=:I~Ssion ~f
c a ~: o"I
o " "! -f n c ra 1 1; f3 V 0 S 4 t Reserves. G- n " F in 6 ro.jo;'~C~q 0 #6?
ol -ruzkw
1. Conmj".Irs-ion for Clas-1, 4,
..Mcati,r, off liiner-P2 T,'.C, - Rp 'T~V-r
Praclit.. Fooait . -S :- C-1,

USSR/kathematics - Representations 1 Apr 53
"Analytical Functions and Open PApresentatims." A. Polak
DWI Val 89,, No 4v PP 617-618
Entablishm pway metricai Kpropertiy of analytical func-
tions., uhich., hwever,, mbraces topological laws intrinsic to open reflections
of a very general nature (A. Polak /ibid. 1(19), No 4 (1936)). Presented by
Aced M. A. Lavrentlyev 30 Jan 53.

POIAX, -A.
Some data on ABO and Ph blood groups distribation in Zagreb and
its suburbs. Act& mod. iugool. 8 no.2:177-183 1954.
1. Zavod sa transfuslju krvi u Zagrebu.
(BLOOD GROUS
ASO groups distribution In Tugosl.)
(RR FACTOM
distribution In Yugosl.)

77
fS _' ` U7_
-tree )eaves. --sandm Polak (Med.
!n PocLr Melt:
All
,.Fbium. 11ii, 'higiit,i "in t', Lip z'., 7'1,,~', %~ai f,,uztd, ut IL:- cs
collected in the fall. Considei-able lw-cs of the glycu~idc,
'bowever, oemrred during drying. Slig'at lwscs also accurred
4rL-ff. -yt~- p iqd~ 'anruk 14_E-__nffler

POIAKY Aleksandra, mgr.
A greenhorn in a 100-yeai-old prescription drugstore. Farmacja
Fol 18 no.14:3~4-340 25 il 162.
;w

POLAK,, Aleksandraj, wgr.
A greenhorn in a 100-year-old prescription drugstore. Farmeja
Pbl 18 no.15/16:370-.377 Ag 162. -)<

POLAK, Artur Dr.
Blood groups In man and their practical Importance. Lijec.
vjes. 77 no.1-2:106-112 Jan-Feb '55.
(BLOOD GROUPS,
practical importance & distribution of ABO& Rh in
Croatia(Ser))
(Ah FACTORS
distribution in Croatia (Ser))

POCILLK, A.
Inhibitor7 effect of saliva on infection by the tobacco-imosaic virus.
p. 362.
Praha# Czeahosloyakia, Vol. 7s no. 5. sept 1958.
Monthly List of East European Accessions (EUI), LO. Vol. 9,9 no. 2.
Fob., 196o,
Uncl,

POLAK.. Artur, dr.
Our experience vith the use of mixed papain-treated ex7throc-ftes 0
in the investigation of irregular antibodies. Voj.san.pregl. 18 no.2:
162-164 F 161.
1. Zavod za transfuziJu Xrvi u, Zagrebu.
(PAPAIN pharmacol) (ERYTHROCYTES) (ANTIBODIES)
(BLOOD GROUPS)

B~-,V-Tii ya.; K,,G.!,!i,
a,.; Ant
163. (MIRA 17. 10)
NefL.L-hoz. 4' nrv8zl,-z

1 26339-65 FWM/VKA W Pab
Acassior. NR; A%-9Io42o75 Z/251-0/6*-;'/OW/004/()107/()1.13
AUMDR: Polak, Augw~in (Engineer major); Behorm, Stanislav JEngineer first
lieut
77.
analyzer-
TIT&
'VoJenske akademie. Sbornik. Rada B, no. 4, 1962, io7-n3
SOURCE: Brum.
TOPM TAGS: numericalcorrelation analyzer, 'correlation function, correlation
signal pattern amplitude, aubbocorrelatioa function., characteristic curve, couriiert
multiplier, integrating circuit, radar pulse, nuxerical multiplication, repeater,
is chronized pulse
yn
The design, operating principle, and operation of a numerical correla-
analyzer are briefly clescribed. The device is intended for the awputation
of the values of correlation functions and carries out the integration of the pro-
duct of two functions in a given Vbne interval. The values of the functions are
given,by the amplitudes of the correlation sigaal patterns. The expressions for
the autocorrelatImEnd the correlation functions are given. The former expresses
the degree of interdependence of the value of the characteristic curve x(t) ampli.
Card

L '26339-6
65
kc=1011 NR; AT,4042075
turlelat a given moment of time t and of the value of the amplitude of the came
V. The correlation function ex-
characteristic curve at the moment of time t +
presses 21kev1se the -degree of dependence of the amplitude of the characteristic
curve XN at a given moment of time t on the amplitude of the other characteristic
curve y t at a given moment of time t. + ,C. From these relations it follows that
the correlator must include an input circuit for feeding the values of the corre-
Ution functions to the counter, a multiplier for computing the product x(t).X(t +
or x(t)-y(t + T), an integrating circuit end an output circuit to record the
of the correlation function for the corresponding value of r. Due to the
V,,ery short duration of the radar pal6eo (of the order of I t4s) which are the source
~o infom-ation, the whole process of correlation estimation must proceed very rap
idly which rocans that the anrily2er must be high speed operating. The analyzer
Qd
tust pass through a preparatory stage in which it assimilates the meth for ed
timatins correlation -functions. For this reason the frequency requirements are
zj iiat particularly bigh. These may be outlined as follv-,Ys- correlation interval
(1 - 105) )As can be autmatically changed by jumpa of I ps (,vrLtb possible pre- 9,
u 4 imation Is
4imimry selecting), 10 pz, and 100 psp the number of prod ct6 r r est
34 - 5DO1 and the opDration interval per product is z 250 ps. A ecoputer was
&osea which is capiible of carrying out numerical mMiplication and addition,
Cord '2/4

26339-65
ACCMIOH IWI: AT40112075
whicb best ensures accuracy of canPutaticns wId the desired speed. Such a device
can be wed for -the study of correlation functi-orms in many fields. The analyzer
operates in such a way that the signal patterns selected by the input circuits
are processed by the repeaters at whose output the values of the signal patterns
are expressed in numerical form, These numbers are multiplied in the multiplier
and the produets obtained are stored in the integrating circuit which, after the
required number of products are obtained, transmits, the result (the value of the
- to'~he output circuit. This cir-
correlation or of the aLrbocorreUtion function) I
cuit records the values in numerical or analogue fotm. A synchronizer controls
the operation of the correlator. The input circuit is stilI in the develoXental
stage and has not been built yet. The pulse counter has a capacity of seven bi-
.nary-series and is constructed with the type 56LNWO transistor. The slm=tion
unit. uses type IOMO transistors and type 511N41 diodes . The frequency of the
synchronized pulses :Ir, 50 kc, the addition time is 20 Iksee; the total period for
the summation of a single product, then, is 140 ysec. The integrating circuit,
which has not yet been built, must ensure the parallel computation of 500 pro-
ducts of the numbers A and B. At the present time the synchronizer is in the pro-
cess of being built and the multiplier is being perfected. The construction of
this special computer, which the teaching staff of the department of radar is
_'~":Card 3/4