SCIENTIFIC ABSTRACT PATRUSHEVA, YE. N. - PATSAYEVA, V. A.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001239510002-8
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: June 15, 2000
• Sequence Number: 2
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

S/I F~,6/(
The extraction of rare earth ... A051/A1710
Taking Jnto account that the analitical coiioontration u,' the cxtra
agent ai 11 bo twi ce tha t u f tht, c qncen t rit I, i un of 1 1,13 d i ii.ur f orm, e
4 ) is rewri t ten f or the equi I i br '"um Boris tan tin the followint- f%,r;!I'.
16 Ig K t- , 16 1t1B I ~(HA] " I
P , - P j rg.
Equation 5) was used to evaluate the equilitrium constant for ittri,-kin,
without taking into account the hydrolyji3 iind dissociution phQnomt~,na.
Table 3 shows the values of the (.-quil~*brium constanta obtained for ittrium.
At hi.-her acidities of the water phase, the drop in the distribut;Jui;
effiGients of the rate earth elements is sl(-xed up, and then a certa4n
crease in their values is noted. The Latter is explained by
with an increase in the concentrution of the hydrogen ions, the
of extraction itself is changed. An ussump-,ion is r-ade that ~It
centrations of hydrogen ions another extrac.,ion mecl.anism is ',res.?nt -0
that indicated. There are three tables, 5 figures and 10 references:
1 Soviet-bloc and 9 non-Soviet-bloc. The fo-ir recent __`n~;Iish
Card 6112

S/18 60/002/005/005/017
The extraction of rare earth .... A051X 130
licatiOn3 read as follows: D. Dyrisen, Acta Chem. Scand., 11, 7, 1277,
1957; L. Selmij F. Fut3s, Chim.ind., 40, 193, 1958; C. F. Coleman, J. Phys.
Chem., 62, 2, 129, 1958; J. It. V. Waror, Pho9phorus and its Compoundi, 1,
N.Y.L., 1958-
Table 1 : (I) Relationihij: of the
europium to the concentration of
centration of HA (in 14); ~4) Diluent;
ENO n tht- %YL-L,-r phase, ~in IA);
Sen.; (b) tonz._,:ie; (
kc) benzene.
distributior, coefficlento of ittrium und
%he nitric a.eid. (2) Element, (3) Con-
(5) Equilibrial Concentration of
1'6) DistribLtion Coefficient K ; (a) kero-
p
Card 7/12

KORPUSOV, G.V.; M;KIVICH, I.V.; ~ATIZUSIIIEVA, le.N.; YERCHEITOV, V.V.;
A LEKSfTEVA , L.R. - -
Regularities in the extraction distribution of rare earth elemer.ts
in neutral solutions. vIks1r.; teor.,Frim.,app. !,,o.2:117-140 162. t, ~
(M.111A 11:~)
(Rart, cartht) (i,,xtr?ictIon (Chem'stry))
I

LEVIN, V.I.; KORPUSOV, G.V.; MAN'K0, N.M.; PATAUSHEVA, Ye.N.; PROKHOOVA, N.P.;
PTATNOV, G.F. . - . . -
Extraction of tetravalent cerium by organic solvents. Atom. onerg.
15 no.2:138-146 Ag 163, (MIRA 16:8)
(Extraction (Chemistry)' (Cerium)

ACCESSICK NR: AP4011239 6/0286/64/0DO/0O2/0O3L4/OOJL4
AUMOR: Koryusov, G- V.; Patrusheva, Ye. N.; Kry*lov, yu. S.
TITIZ: A method or europium extraction. class 120 No, 159811
SOURM ByU. izobrete i tovarn. zaakov, no. 2, Jo4, 44
TOPIC TAGS: europiumY europium extraction method, eleme*nt Aaction method,
rare earth e]A=ent,, ram earth metal, rare eva-th metal extraction eurol4um
~extrsction
UUMIATION: The patent describes a method of extracting europium from a mixture'
of rare earth elements by treating their aqueous water solutions with a reducer,
~for example with zinc dust. For raiving the separation factor of the europium, the
,aqueous water solutions, after reduction of the eurapium, are subjected to extrac-
.tion by means of an agent such as te.Lbutyl phosphate*
DATE ACQ: 14Feb64 SUB CCDE: EL ENCL: 00
suxa=w: 2TNov62 NE 1W SOV: 000 OTHER ODO
Card

PA-TSAYE.VA, V. A.
Calculating the fluctuations of the horizonta' velocity of t,',,
wind in the free atM03phere based on radioi,ind observations.
Trudy TSAO n:.41:82-85 '62. (MIRA 16:10)

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~ , ~'4. W11,A A:1.

ACCESSION NR.- AT4035164 S/ODDD/63/000/000/0195/0210
AUTHOR: Korpusov, G. V.; Patrusheva, Ye. N.
TITLE: Extraction metho-J9. for the separation of the rare-earth elements
SOURCE: AN SSSR. Institut geokhImil I analitichoskoy khImll. Redkozemel'ny*ye
elementy* (Rare-earth elements). Moscow, lzd-vo AN SSSR, 1963, 195-210
TOPIC TAGS: rare earth, rare tarth extraction, rare earth analysis, cerium.
promethium, eur9pium, yttrium, tributyl
ABSTRACT: In an extensive review of the extraction and separation of the rare-.
earth elements (cerium, promethium, europium, yttrium) with neutral organophos-
phorus compounds such as tributyl phosphate and diiosamylmethyl phosphonate, the
authors discuss the equilibrated separation of the nitrates between two phases,
the kinetics of the establishment of this equilibrium and the dynamics of the
separation process. A study of Vie distribution of the individual elements gives
basic Information as to the composition of the extracted compounds the relation-
ship between the distribution coefficient and the composition of the phases, and
other characteristics of the system. Data on the variation In the tributyl phos-
phate ratio during the extraction of rare-eartl~ elements of the cerium subgroup
relation to the concentration of the salting-out agents are tabulated. The

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KORTHALSP Edmund; P;.TWY, I-och
Contribi,ticn tr, th,~ stuty of fnfect'ons '-n F.'C,7,&'
f
pri.ctice. Wiad. lei,. '18 ric.11:1~31-934 1 -7e '65.
1. Z Katedry Stornatologii 2 Cent.r. Sz~itala Min. ',-,Iojskowe.1 41X,
(Kieroi,nilk: doc. dr. E. Korthals'~ .

PATRYN, Janusz
Retroperitoneal cyst orginatng from *.he urogenic
Pol. przegl. chir. 36 no.8:1025-1027 Ag 164.
1. Z Oddzialu Chirurgicznogo SzT)itala Wpjskiego w Wielunlu
(Ordyntitor: dr Z. Patryn).

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Speclat Features of the Production of Shart-LICe
"aratima
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--XAMMMX,, A.A., inzh.
Production of agloporite in KarapMa. Sbor.trud.VNIINSM
no.6tl5l-158 162, (KM 15s12)
1. Kara andinskiy sovet narodnogo khozyaystva.
lKaraganda-Aggregates (Building materials))

PATRUT, I.; POPESCUP M.; TEODO=CU, C.; MOLNkR M.
-------
Geology of Moasio Plattom. Stratigraphy. Petrol mi Faze 12 no.11'.
481-493 N 161.
(Rumania-Geology, Stratigraphic)

PATRYN, Fmil, dr.
Inalysiv of thn factors influencing choice of
and ways for goods in the Polish foreign trade. Tech gosp r4orska 11
no.5:131-132 '61.
, 0
~. Ozkola Glowna Planowania i Statystyki, Warszawa.

PATRYS, Janusz-
' -
Artnm7 cancer of the smll intestine. Pol. przogi. chir. 35
no.5:519-520 163.
1. Z Oddzialu Chirurgicznego Szpitala Miejskiego w Wieluniu
Ordynat-or: dr Z. Patryn.
(INTESTINAL NSOPLASMS)
(INTESTINEY SMALL)
(SURGERY, OPERATIVE)

PATRZALEK, Zenon, mgr.jinz.
The machine toolB factory in 'rarnobrzeg. Przegl mech 20
no.19/20:602-,603 161.
1. Tarnobrzeska Fabryka Obrabiarek.

PATS, 135(-.
the occasion of M. V. Goftman and .4. 1. Golub's paper
OCatalytic oxidation of basic pol7cyclic compounds of coal
tar and its fractionall Zhur.prikl.khim. 30 no.8:1264-1265
Ag '57. (MIRA 11:1)
(Oxidation) (Coal tar products)
(Goftman, M.V.) (Golub, A.I.)

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0
0, 0 0 0 0 0 0 a a 0 0 0 0 to 0
0244
to 0000 00 0 to 0 0 0 0 0

FITS, B. M.
-- -
On the article of N.M.Karavaev, D.D. Zykov, IU. N. Garber 'Study
of phase equilibriums in the system: naphthalene --/3-methyl-
naphthalene. Ukr.khim. ftim. 22 no.2:265 156. (Muk 9: 8)
1. Ukrainakly nauchno-Issledovatellskiy uglekbimichoskiy institut.
(Phase rule and equilibrium) (Naphthalene)
(Karavaev, N.M.) (Zykova, D.D.) (Garber. 1U.S.)

77,77-

1-A -

AUTHOR: -Pats, B',M. 68-5-8/14
TITLE: Comparison of various schemes of production of technical
naphthalene. (Sravneniye razlichnykh skhem polucheniya
naftalina).
PERIODICAL: "Roks i Khimiya" (Coke and Chemistry)y 1957, No'.5,
pp.39-41 ku.b.b.h.)
ABSTRACT: Present methods of naphthalene production are outlined.
The distribution of naphthalene in various fractions during
industrial distillation of tar is given in Table I and the
composition of the naphthalene fraction in Table 2. Mech-
anical and rectification methods of production are compared.
It is concludel that with the first method 98% technical
naphthalene can be obtained from raw materials of Vie South-
ern and Eastern works and with the second 97% naphthalene
from Eastern raw materials and 92% from Southern raw mat-
erials. If intermediate produe-ts are also treated the first
method gives a 96% yield (on naph-thalene in the initial
fraction) while the second method - 9D%'. Moreover, the
second method requires washing with concentrated sulphuric,
acid in the proportion of 13% of the initial naphthalene
fraction. Costs of production are lower for the first
Card 1/2 method. Thus the mechanical method appears to ha-we a rumber

PATS, B.M.; SHILINA, N.I.
Economics of the production of phthalic anhydride from various
grades of industrial naphthalene. Koks i khi-m. no.2i43~48
964. (MIRA 17:,,,)
1. Ukrainskly uglekhimicheski)- Institut.

PATS, B.M.
Discussing K.M.Vaisberg and others' article *Use of gas-Ij-;uif.'
chromatography for the analysis of the composition of vnrlous
naphthalene containing products." Koks i kbim. no.3:60 164.
1. Ukrainskiy uglekhimicheskiy Institut.
4qRA 17-4)

/ I,- I- I I/, /
I I
VOLIFSON. B.U.; PATS, B.M.
V.M. Temarin's nethod for designing naphthalene fraction
cryvtallizers. Koko I kh1a. no.8:63-64 '57. KLRA 10: 8)
1.Ukrainskiy lekhtmichookly institut.
~Gryetalllzatlon) (Naphthalene)

PATS P B.M.
Coal-tar phenols and processes of their recavery. Zhur. V'U!O 5
no.1:3~-38 160. 4UTIA 1i,: 4)
(Coal-tar products) (Phenola)

3/06 3/60/00 5/0(j I /XX
A051/AO29
AUTHOR: Pats, B. M.
TITLE: Phenols of Coal Tar and Means of Their Application
PERIODICAL: Zhurnal Vsesoyuznogo Kh.Lmleheskogo Obshchestva Im. D. I. Mende:eyt-1,
1960, Vol. 5, No. 1, PP. 32-38
TEXT: In 1957 world p,oductia-i (not including the USSR) of phencls based
on the products of coal coking was no less than 100,000 tons. The processing
method has a significant ei'fect on the yield of phenol produced from coal (Ref, 1,1
The phenol yield obtained by the 3 main methods of processing is shown In Table 1,
It is seen that the hydration method gives the highest yield a.-d the coking met-hod
the lowest. In low-termperature coking of coal, resins with a high phenol ('.ontent
are formed. This fact confirms the known theory on thermal reactions Df phen.,
dealkylation and formation of hydrocarbons from them during the high-temperatur-
coking process. Fig. I shows that w1th an increase in the temperature in the
pyrolysis chamber the phenol yield drops and that of naphthalene increases. Thes~-
regularities are also confirmed In Industrial practice of coal coking. Phenols
obtained from high-temperature coal coking mainly consist of mono-atomic phenols,
Card 1/7

3/o63/60/Dri5/0r, 1/0 1 C/~, I i~'/U
Phenols of Coal Tar and Means of Their Application A051/AO29
which renders them different from pherols obtained from semi-coklng, lIgnItes,
peat and shale tars, where in addition to mono-atomic phenols multiatomJc oneb
are also present. Coal phenols consist of many other oxy-compounds found in the
resin in addition to phenols,cre5ols and xylenols. Phenols, such as i3o-p6tvuL1o-
ouminol, symmetrioal m-methyietliyiphenol, .3, 4, 5-trimethylphenol were shown to
be present in the tar (Ref. 6) . Amongst the relatively little investigated
phenols of the anthracene fractions the following were found to be preseqt:
oxy-derivatives of diphenyl', diphenylene oxide, fluorene and phenanthrene. The
tar waters in coke-chemical plants are considered to be a valuable phenol so,_Irce,
especially of phenol and cresols, s1nee they partially dissolve In this water
(Ref. 14, 15). The alkaline method is the most universal one for phenol formatlor)
from fractions or oil. Phenols have a different acidity depending on the number,
size and position of the alkyl groups. This property was the subject 01 r1U.M-3~rZDUs
investigations dedicated to the select:.ve extraction of phenols (Ref. 1) The
alkaline method of phenol extraction from fractions or oils Is complicated by t-he
many phenomena accompanying the main process, suih as: the. colloidal dissolution
of neutral Compounds in phenolates, emulsificatlor of oils In phenolates,
dissolution of phenolares in oils, hydrolysis of pKenols, formatJon of 1-omplex
compounds from phencls and alkalies, etc. The author stresses the face that t~ie
Card 2/7

S/063/60/uo"/oo I -If-x
Phenols of Coal Tar and Means of Their Application A05!/AO29
application of effective extracting apparatus opens many possibilities for uEing
other phenol-extracting methods beside.5 the alkaline one. Phenols extr~t(:ted froff,
coal oils contain admixtures, such as pyrid1ne and quinollne basel;, neutral hyJ,
carbons, sulfur compounds, etc. 'hey require speclal purifying metnods _1~
elimination of the thiophenols causes particular difficulty. Their prel,ence in
phenols obtained at coke-chemicai plants in the South of the USSR is shown ill
Table 6. It is pointed out that the t.hiophenols are unwanted admixture, ,
ly those with a high boiling point, whioh cause ecrrosion of' the equ lipmert use! in
the rectification of phenol's (Ref. 21). In order to obtain phenols from phenolaij-,s,
the latter are most frequently decomposed with carbon dioxide, This method allcws
for the regeneration of the alkali from a sodium carbonate solution, whl~_h is
formed from the decomposition of the phenolates. Rectification is the f1naL stage
in the production of phenols. Considering the complex composition of the initla,
raw phenols and also the demand of consumers, the modern set-up for rectification
ensures the production of a wide variety of phenol products. A number of phencls
having close boiling points require sj:ecial methods for theIr separation, where
the different acidity of the phenols Is utilized, as well as the different rate of
hydrolysis of their sulfo-acids, et.c. For example, in order to separate the m-
and n-cresols and isomers of xylenols, the extraction method, sulfonaticn and
Card 317

S/063/60/005/CC11/(, F /'c lrj,/)a
Phenols of Coal Tar and Means of Their Application A051/AO29
formation of molecular compounds are recommended, as well as the formation of
tertiary butyl derivatives. ConsidprIng the oomparatively great ext,ent of phenal
processing, lowering their loss durinq; production can serve as an important source
for Increasing the resources of phenol products. The main consumer of coal phe-nol's
is the phenol resin industry. The rate of reaction and the reactivity of the resin
depend on the nature of the phenols taking part In the reaction of semi-condftnsa-
tion with aldehydes. Data given in Raf. 24 show that for the production of resol
resins tri-functional phenols or phenol mixtures containing large quanti.ties of
these compounds (phenol, m-cresol, 3,5-xylenol) should be %ised. The different
reactivity of phenols presents a roblem for the coke-chemleal industry in supply-
p
ing the plastics industry with phenol products with a ccnstant composition and
consisting of as few components as possible. Alkylated phenols -~ontainlng com-
paratively long side chains yield interesting resins which are compatifile. with
fatty oils and soluble in hydrocarbons. A large quantity of phenols, -8.rt,1f'1i1ftr'1Y
cresols, is used for the production of etners of phosphori(- cl2ids in tur-,-
as plasticizers and soiven*~s (tricresolphosp"ate), 1!~V'F~stigatic'nb .0
Vh,at by halogenating xylenols, the bactericidity of phenals (Whig!. ?~as t-6er, !cr'~wn
to exist for some time)caan b,~ increased by several times, At the prese.~t time
various bactericide preparations ar- obtained tased cn pherols 3, their
Card 4/"7

S/053/60/005/00 1/0 10/03 1C/YY,
Phenols of Coal Tar and Means of Their Application A051/AO29
It Is stated that phenols directly or their derivatives (diphenyldithlopliosphoric
acid) are effective reagents for the flotation of non-ferrous metal ore S)nd coals.
Surface-active substances and tanning materials are synthesized from a phenol base.
Some phenols are used as anti-o*dizing precipitating agents for fuel oils and
synthetic rubber. In analyzing the production problems and application of coal
phenols, the author makes the following suggestions: 1) increasing the phenol
output by reducing their losses during production, 2) increasing the variety of
phenol products, 3) improving the quality of the phenol products, 4) developing
methods for using larger quantities of phenols with a high boiling point which
have not found application until now, There are 11 tables, 1 graph and 26 refer-
ences: 9 Soviet, 4 English, 13 German.-
Table 1:
Phenol yields in varl cc 9. from 1,000kg of dry coal):
Ous 40cessing methods (ino
ooki3ig - Koxcoss semi- nanyxogemWboking hydra- r"xxii-ximetion
1M.... _t -
Phe ls ar I I P, e, ~,O,.~ W tar ph-enol- Ph'r
'PC I ";:
114*4 bKWC
CNOAN tot WDdw~ 'I t.,r., I '1'C ' t acero
waVrs -.a-1 C__ zvvws ota I oil WAV'rs I otal
Phenol
(DeHO.11 . . . 10.05-0.25 0.05 0,10-0,30 0 1
0'I5
OeHOAN _Cs 10,2-0,85,1 0.12 0,32-0.9-"l 5," 0,50
Phenols
Card 5/7
0.75 7-9 2 8,2-10.2
5.50 25-35 '1!5 27.5-37.5

Phenols ol," Coal Tar 3r.J Ieans --f Their Applicatim
Table 6;
Sulfur content in phenol products
designation Content 3, in %
Pherols from the phenol fraction 0.05
Phenols from the naphthalene fraction 0.07
Phenols from the absorption fraction 1.38
Phenols from the anthracene fraction 1.41
-"'ri-cresol 0.06
Commercial xylenols 0.14
Card 7/7

PATS, B.N.
S7nthotIc surface active agents based on coke chemical
rew materials. XhIm.prom. 2-109-112 My 160. (MM 13 :7)
(Surface active agents)

PATS. B.M.; IMIOMbTYASHCHAYA, A.S.
Thionaplitheas, a sulfur compound associated with naphthalene. Lhim.
pron. no.8:666-668 D '59. (MI3A 13:o)
1. Ukrainskiy nauchno-issledovatel'akiy uglelihimicheskiy institut.
(Thianaphthene)
(Naphthalene,'

-011/1-1- -
-K 12:~
A.,3. an6k
of' kiathracene 1.'r-action
N1. 9, PP 'IT
A i~- 1,Lu~-'Z: 601ULilitiv--~ 01' cu.Lbuzole :,rd pht--,ant.-,i.ene in
ar -ne oil viere deteii;iiie iCure 1) and t'i'le process
of crystaili--aLlon of fY,;LCti,)n 11,lvr~,,?tlolted.
'I'lio ol)G~iliil.ld Lb!1L oil (.,mblillc Of L111'.
j.,,ic,i,L, frucLiun, ti,- -,oiid phase is formed ;z-iinly from,
Un-U.Zack~,ne, cur~azo -Le, phe,,-i&nthrene, fluorene and diphen~rl-
sulDhide whicf. form sclid .-Iolutions. All ot,'-.er compounds
in tliu liquid pliase am, only auu to thu presunce of
vst-
the Latter in the prcKiuct are usually i':)und in the, cr-
al lisea material. Step-wi--e ci-7stallisat ion or cr~~stall-
isation in the presenco~ of L;olv~nts per:ait reducinC, the
yield of raw -~iitnracene -ard jmpi~ove its composition ('--ubles
4 and -Llie fine crystalline structure of raw antLa-
ra--ene i-L cau--~ed by a low content in the anthr-icene fraction
of coi,~,oncmts, prt~.,.ence of benzene insoluble
s-Libstance-, (w~iici, act 16 cry:3tallisatioii nucl(~i) and a
lar--c 1?ro~jortion of -LL.-. fi~:~ tion tToilinj-, -bove 3600-C
C-~
d t' 0 f LL,; medium. '.2heref3re, in order

212- 2
ysL- 1: of AnLixtmno
~,C 03tair. uLtLili fLi~U11'eu I'c~ -.', ~Lnt Iii-i cen~- Oll r-(D:~ L
is--~ illat ion plarrL: -J-, 1~j '1~7, - -1 1- C.
-~-nl.y tli,-f r t ,)np il~
mitu),d to Cryl-Lldli-b-ti )1~ L-~bje C))
table.,~, -and
aru 3~)vitzt LrLd L xeruar-
i i Uj; U~-dN

PATS, B.M.; KRU)PNOVA. L.I.
Bloctrometrtc method for datermining salts in ttr and tarr7 water in
by-product coking plants. Koks i khtm. no.10:44-47 ' 58.
(MIRA 11:11)
(Salts--Analysis) (Goal tar)

IJLL t SB. hl.
a,,--,d '.-ich., I."-.
21.2i'VI: On aleciinical iiequi.ceiaen~;~3 from 00al 2ur u-JiL sej
the Preservation of 4~vood (0 tedi-niches--likh -.rc-bc-;!7.Tj -r--.
k kuueanouEollnpa iiu~llam dlya -ant ise pt irovlLni,,--i
drtevesiny)
19"
\.~n tilt. baLii~ of
cDu.,~umeri~ rei~aidinL- pi-opemLes of oils --c-a f'3-
U-ion of "VoOd a.--d I -L%~ - ~L -~
pre se rva4 poss sib il4t 0~
co,dnt~ indus-ur-i
prepart~d a ~ioject Df new c o
tal, oilL, suitublu foi, Liiu stable 5).
5 table6 uiid 2 ivf~j:[-ence,,~ of whicl,~, 1 is Jovictl a--
1 German.
,ard 1/1

AUTHOR: Pats, B. M.
TITLE: Rcvi~~m of Lhe book of Ya. A. Bi-on "Operrton: f
Pipe Still fur Tar Dist illaticr."
kn-16u Ya, A. BrDna "Apparatchiki trubchnLo-o
s--clopere-onnot~' agregata")
C)
PERIODICAL: Koks i Khiiziy~), 10,58, Nr 4, pp (:-~L-~4
ABS'-"R111'T: T~, k if7, 1
Liter
Card 1/1

AUTHORS; Pa to ~ B. M. anu K~1~-,pkc ;a. ~1, I T .SGV/ bi~ -- 5 8 -- 10 - 14 12 5
TITLE. An Ele,.~t---,)metrL,L Me-ti-ic-1 :,f' Detefm*,niiiE, Salts in Tar and
-^cking W,~rKr, (1E!eV=ouietrichesk!y metod
oprede-lenlya sloley v snlc-.e I nadsmol noy vode kokso-
khlmicheskikh Lavodov)
PERIODICAL. Koks i Kh2-mlya, 19'E. Nr 10, pp 44 - 47 (USSR)
ABSTRACT: A met~aod of determining the Tc-tal .ontent-3 of salts in tars
amd liquor based. on the measurements of conductivity
was deveioped. The results obtained by the method are in
good agreemeLt with the determi.Aation.3 based on dry residue.
The method is described --'In come detail. There are 1 figure,
6 tables ai-d 6 Soviet rofererwes.
Card 111

AUThOR: Pats, B.M. -D-12/21
TIT13: Thermal Analysis of Solutions of Naphthalene in Coal Tar
Oils (Termicheskiy a-i-aliz rastvorov naftalina v kamennou-
Eolln,ykh maslakh)
PERIODICAL: Koks i Khimiya, lc)5B, i,r 2, )p 50 - 51 (USSR)
AI~Z)T-Ii'~`.CT: A study if the te[m.)eratire if crystailisati3n of
ions -in coal tar Dils (phenolic,
naphthalene solut' naphthalene
and absorption DI ls) in the ter-.erature region 60 - 80 OC i,.,as
carried out. The results obtained indicated that the behaviour
of these systems is near to the ideal. On investigation of
the usual ~in -,racticce) ~olu:ions of naphthalene in coal ta-r
'Dils, satisfactory res,,ilts can Le obtained when upinr! equations
aT*)plicabie to cojacentrnt.,d sol,itions. There are 2 tai-bles
and 4 references, 3 of ire Soviet ajid I Swedish.
ASSOCIATION: UIMIN
AVAILAB12: LibrarZi Df ConC,resS
Card 1/1 1. Nnphthalene crystals - Tempera,~ure fjctors

"kATS, B.N.
Review of IA.A. Bron's bcok "Operators of tubular furnaces for
processing coal tar.' XDk;o i khIm. no.4:63-64 058. (MIRL 11:4)
1. Ukralnekiy uglekhladchoskiy institut.
(Coal tar)
(Bron, IA.A.)

ALJTH ORS: Vollfson, B. N~, LLnd Pats, B. MI. 68-8/23/23
TITLE: Remarks on the method of C-ilculating Crystallizer3 for
Naphtb-a2ene Fri2tIons, Proposed Ly V. M, T-anarin. (Pr,
pcvodu metoda ],a3-~hetu IrristaJ14 zatorov d1ya naftsdinor
yk-h
frak'lsiy, predl-.--heant,Lo V. M. Tamarinym).
PE.-UODICAL: K.-As i Khimiya, lt)~17, No.8, pp. (3-64 (USSR)
ABSTRACT: This ~-i a uf ~h~! papr!r by V. Ml. TamarLn, published
in "Ko'r:s i Khir,Lyall, 391)7, Nr.l. It is pointc-d out that in
-C fG-MUla fOr r-'LiCU1;1t ni: irLm cr,~sl-llizers the original
auther m-iJe a r.-isic error ir. the inteGr-ltion of the eq,.zation
for t1he he-A balai,ce of the f-.1ementarl layer In which the
'OVIPCI-atUre difference (tk-ti;") was assumed as constant. 1n
fact '!~ (tempe at,-re of crystallization of the fraction) is
constant while 1,01 (wall temperature from the side of the
Pract-on~ is var4'-.ble, depend:~nk: or. the film thickness. In
the culcaliitions tht lu.~ ci- am
I yst---dlizer, V. M. T ariri did not
ta-~e into consi3e7ation differences in the heat transfer from the
Card 1112 SU-r!1("e C~f 1,11(~ li,,Uid u)d 1-h- wall. The --ev-'(,-w is

68-8-23/23
Remarks on the Method of Calculating Crystallizers for flaphthalene
Fractions,, Proposed by V. M. Tamerin. (Po povodu metoda rascheta
kristallizatorov dlya naftalinMich fraktsiyp predlozhennogo
V. HO Tamarinym).
unfavourable. There is 1 table., 1 figure and 6 re-
ferences, all Slavic.
ASSOCIATION: UKhIN*
AVAILABLE: Library of Congress
Card 2/2

R.. to'----
Gos. No c pgsl. Timt, Allft IM, (10). 358-302-
hunl(Aim.,1900,A
CA trm; a 8!,ngle
~anA laad are doicitnined in mcbjfii,
":-welghbig. Thallipul -is ficpsridclt~. tracting
byl.,CDx
romida: with ~Ctbcr and potaro
th
~Cfl soln. -.. Lemd
grlphically in. aq~ - 1 #
.mnains envrcly m-the M, tbase Is determined
The reducinji pd tia)l tro-
3 N MI;
-vs. t6e R. Lmm
0-40 V, Ph 0_44-v,
W,
J;

SOV, 1 17-~8- 8-18178
F, ar. a ii on I rom- Re I er at i,, nv~ z h urr-j I, Met a I l,irgiy a, 19~,8, Nr 8, p 28,1 ( TI*SSR)
AU rHORS- Arcl ,c a F V P ats. R. G
T I'F L E - Amperometric DrIeri-nin.iltun of Chroriiiurii, Vanadiun,,, and
Manganese in Filanium Alloys (Arnperon-letricheskuye opredcle-
vl.,~e khrunia. %ana(hya i margantsa % titano.ykh splavakh)
PERIODICAL- Sb naLlkhri. it- Go~- n. iin I tsvetri. vnet. , 19~8, Nr 14.
pp 74 7 11
ABSTRACT The teasiljilLv,~ o arnperornetrIL titration of Cr, V, and Mri
1ram the _-,ame fcst sarnple :ri tile presence of a 200-fold excess
of T i's establisKud 'rhe titration is c--irried out with an 0. O;N'
~101dlloti uf Mohr t,alt at + 1, 0 v and an - 10 acidity. 'I'll e
i a i v () I r o t.t t , o ni !i v P I v I c t I r od v is 0 0 0 - 8 0 0 r 1) n i. Fi
the sum C r + V -4 M n i s I i! rateG atte r thei r oxidat iuri with
(NH4) S 08 in the presence of AgNO_j- After the titration the
solclt;on is aga,n ox,dized with (INH4)2S208, the Mn04I
decomposed by the addition of NaCl, and the surri Cr + V is
I it rated rhut, triv V41 ~.s oxidized xith an 0. JN solution of
KMn04 the cxccss of vvhich is reduced by the solution of
Mohr s salt and the V is lorated. Mo and A I do not impede
Card I I the determination. 1. Titanium-Determination N G
2. Meta-Is-knadysis 3. bociium arson ate-Applic ati ons
4. Iodine-Titration

PATS, R.G.; SEMOCHKI A, T.V.
Rapid polarographic method of determining copper, lead,
cadmium, and zinc vith the use oir an alternating current
polarograph. Sbor. nauch. trud. Gintsvetmeta no.19:808-822
162o (MIRA 16:7)
(Wonferrous mgtals-Analy5is)
(Polarography)

PATS, R.G.; VASILITEVA, L.N.; ZAGWDIIIA, T.V.; SIIUVU(.VA, Ya.D.
kolaxographic determiruition of lead axic teliurium in techmcal
selenium. Zav.1ab. 29 no.8:92e-929 163. (i-IIRA 16:9)
1. Gooudaxstvernyy nauchn(>-isaledovatellakiy institut tsvetnykh
nmt&llov.
(Load-Analysia) (Tellw-im.-Avidysis)
(PoliLrograpliy)

S/O32/61/G27/CC1x/CC6/C_2-1
ill 1 ripn~
AUTHORS: Pats, R. G. and Tsfasman, S. B.
11"
TITLE: Determination of indium by means ~f a. c. ,olaroGraphs
PERIODICAL: Zavods?aya laboratoriya, v. 27, no. 3, 1~61, 1,66-271
TEXT: The authors developed an accelerated methodfor the jolaroCra-hic detei-L
mination of indium. The studies were conducted with the aid of a polaroj-,raph
of the type "Mervininstrument", model 3. The bottom mercury was used as an-
ode. The cathode used was a droppin67 mercury electrode (2-8-3.5 drops p/sec~
j PO
A mixed 1113r (13~,.') - 113 4.('V") volution was usod at) indiffert,.)nt back-round
electrolyte; durinE experiments this solution was found to be optimal. Under
such conditions it is possible to measure u~ to 1o-7 moles of In. In can
still be determined in the followin;- ratios to other metals in the solutiDn:
Fe In = 30,000 : 1; Pb : In 1; Sb In 60C : 1;
Sn In - 250 : 1; Se : In . 60 : 1i Cd : In 20 1; Te : In = 1 : 1. it
should be mentioned that indium zan also be determined in the ,,resence ~f
cadmium. The ori3inal pa --er Cives tf.ree detailed analysij prescri.-tior3 '-r
the determination of In (in sa7i~le3 V/it'! FC : In30,OCO : 1, rt~s.e-7!tive-
card 1/"

PATS, R.G.; TSFAaWv S.B.
Determination of indium with an alternating currentpola-- . Zav.
lab. 27 no.3:266-271 161. RIA 14: 3 )
1. Goeudaret-,----Myy nuachno-iBBledovatel'skiy inutitut tovetnym
metallov i TSentralluaya laboratoriyu avtomatiki.
Undkam~-Analysiv)

0
AFM TIVA9 T.V, POZDNTAKOVA. A.K.LPATS, R.G.
Pol.Lrographic determination of rhenium in solutions. Sbor.nauch.
trud..GINTSUTXICT no.12:94-98 '56. (HURA 10:2)
(Rhonium) (Polaropraphy)

Aftl' A. A.
xj
j v 77
NO.,
grik AfW loss. No, to,-,-I
Zkw.i KrAl
i4 I.
or
6171 anil Fb d1j*t
or J~wa the ba*
Ah T
wr
Ou
wan ewcfMI
4 -and I
,is
bY
I
S4
7 -1

I
Alw -71O.-For poto 'hic dctd-
1956. Ar. No, rosrap of
tit
X1, PW and Za lu tUc vuether Ornot contlf, tl
141.6
6~601MA 92:nqw ;vigla amd, by
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of cutst,
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Oil
Oln
Aker

,,/ ,//I .---, 11,(/.
KLKLHIURS. A.I.; ZAGWDIHA, T.V.; SMWALOVA, To.1p.; KIMKO, A.N.: PATS,
R. G.
Nov method for the determination of zinc in aliuninum and eilumin.
Sbor.nauch.trud.GINTMTHET no.12:138-143 '56. (HLHA 10:2)
(Aluminum--Analysis) (Zinc) (Metallurgical analysis)

-- - --------
M~r b-'r-A-l"o Zfttrmlme,~im

A' tf, Nz);4
I-z

,
Cd ~nd
i J!, ~:air balk
fc,w
j
.
-
y
0! il'o 7a wit'l a dro;ipw,
*
The mc~ 6 o-I pc
6N. trode. thfA allows 0,001
r
ddermimd with.
ant, of in Cd to V-
-
an- ollvex- it with
nilliQla-f th
a
l
'
It On ht)

p

PATS R.G.; TSFA~HAN, S.B.; SEMOGHKINA, T.V.
Determiftion of Cu, Pb, Cd, and Zn In the produsts of nonfar-rous
metallu gy in an alternating current polarograph. Zav.1ab. 29
no.4 :39 401 163. (MIRA 16:5)
1. Gosudarstvennyy nauchno-issledovatel'skiy institut tayetnykh
metallov I TSentral'naym I&boratorlya avtomatiki.
(Hetals-Annlysis) (Polarography)

7.HDANOV, S. I.; PATS, R.r,.
Polpriw--%:,% '~ or L-, L I, urilva , ,Ii - t 2 . T?;~3-ra I ~ n'. t- 1 l.- ' I-M. -. -,,~ < * -*~p -
khi-mll-a 1 no.9--'ry92-I'Y:)6 3 1659 ("414, 18:131
1. Gosudars'~V*Mnyy imtit-ut t.-3vBtn7U metzilav.

PATS, R.G.: AREF'YEVA, T.V.
Polaxograph,L: method of pj--~--'7Lm d ~a~a ~ = , n
ar
copper-nick,el production shn.-3t3. Sbor. nauch. trud.
Gintsvet-raeta no.18,-,"13-93 *61. O.MLA it,. -
(Polarography)
(Platimun-Pnalysis)
(Pa-Iladium-Analysis)

PATS . R.G.; SMOCHKINA, T.V.
Polarographic determination of lead and cc;, r tee,hir and
. pe
in a tellurium concentrate. Zav.lab. 28 no.7:800--801 (MA 15:6)
1. Gosudarstvennyy nauchno-issledovatellskiy institut tsvetnykh
metallov.
(Lead-Analyois) (Copper-Annlysin) (Telluriun-Analysis)

r
i ql.
WIF
!~nt A,
Ap
R
0~!q -4
-Ant', rmllm
1 -4
m
wzpi t-,5ij F.of)ty,tj AX
A), thl!i rMtWyl Ll
Tilt MM!
4
the it
PMA 01,111d,31k
lye vqjjjj,tj -t ivy 2 lnfAl~,Idt~-
lln~v%j
;zz

PA TIS p R ~ G. _ _
Use of square-wave POlarorrT-aphy for determininp, cadmiim and t~ajjjur,
in products of nonferromi metallu?-F -20 '( ,
,Y, Zav.lab, 28 no.1:19 2
(MIRA 15:2)
1. Gosudarstvennvy nauchno-inaledovatel'skiy Anotitut tsvetny-kh
metallov-
(Cadmium -Aniqlysis) (Thallium-Analysi s)
(Polarograpby)

ZHDAnOV, S.I.; PAn
~21--&-a-
Polaropaphy of tellurium. Part I., Tritrave-lent t6illuritim, Eleili-c-
khJniia 1 nc,89947-95i, Ag 165. (Mll~ll
1. Gosud&rst-vennjy institut tsvetnykh met&llov i InstiiLt elektrc--
k.himit AN SSSR,

MAKHACIIEK, Z. [Machacek, Z.1; MEYZLIK, Y. [Mejzlik, JJ; PATS, Y. [Pac, .J
Anionic polymerization of formaldehyde. Part 1. Vysokom.soed. 3
no.0:1421-1426 S '(I. 04IRA 14:9)
1. Nauchno-issiedovatel'skiy institut makromo)ekulyarnoy khimii
Brno, Ghekhoslovakiya. (Formaldehyde) (Polymerization)

I' ". -7 , "' " .Y~ . , - 7.-. :. ( T a ; , : , I.-)
. 1 -1 - -
sta:-,; ~' - :~~ I - - . . . D I r
(" - - '.. - ~ : 11)

PAT".j,'CV,xl . .
Ultra Linear "mr1ifier. Aadio Enrineor"ni-, 173:1',:~-'~~u~.55

ARTAMMIOV, Alek-sandr Yakovlevich [A-rtamonov, Olaksandr LAkovlevichj';
AMBLINJ 0., red.; PATSALYUK, P. (Patualiuk, P.). red.
0,~ Z- -- -- * ,
(Tolerances. fits. and technical measurements] Dopusky, pc~tpaffi-.y
I tekhnichni vymiry. 4tv, Derzh. vyd-vo tekhn. lit-ry URSR.
1958. 405 p. (MIRA 11:11)
(Macb1ner7--Deeign)
(Tolerance(Lnginmeringv
(Mansura t ton)

PATSANDVA, Te.
Correspondence of two apartment house offices. Zhil.-4kom.
khoz. 6 no.6:8-9 156. (MLRA 9:12)
(Orskhovo-Zuymvo--Apartmnnt houses-Managmmmnt)

YUh6)"m)# A.A.; PAFSAROV6KOA, Cs.6.
V~ k t or I vanw! cl~ Nodr' ,a: (;v; f,ri tn~ c!-jrit~7rmih i of hir b: rir,.
7,hur. m~krob~ 31. v o--W,j. I i~nffrtxrj. 4110.1 1 slt,4-Li," N 165.
(MIKA
1. tW-3titUt OpitilMi0iOtfli i IRIKI-Obj( lf)V~i !Metli GEtmai-li A~41N
i Do s ka ya po'~ L k, l a ;7,1.,
January 26,

n I r c) ng- ~l s i - i
'~)UK--)V,na. Ilfst. ven. 10
'MTRA

I
P.VISA~,E,NYUK, 0. V., CInd Mod Sel -- (diz;s) "Materials on the complex examination of
children born of mothers infected with or previously inNcted with syphilis." Gor'Kiy,
1960. 19 pages; (Ydristry of Public Health RSFSR, GorIkiy State Medical Insitute i-meni
S. M. Kirov); 200 copies; price not given. (KL, 50-60. 136)

'I YA, 0. A.
UGH AS TH ll~ I k, V
~t3p-j(j; 4 ~b,

~z
rc yr 7. f!
tt

YANITSKIY, I.V. CJanickis,J.1; PATSAJSKAS, E.I. [Pacauskas,E.]
Electrolytic oxidation of selenotrithionates. Liet ak darbai B no.l:
143-152 160. (EFtl 9: 10)
1. Kaunasskly politekhnicheskiy Insitut.
(Selenotrithionates)

/"/-/ / -I-) // t 1) ~-'P ~, / .-/
YA11ITSKIY, I.V.; ZELIOXAYTI, V.I.; PATSAUSKAS, R.I.
Analyzing mixtures of some oxygen compounds of selenium and sulfur.
Zhur.neorg.khim. 2 no.6:1341-1348 Je '5?. (MIRA 1C:10)
l.Kaunaeskiy politekhnicheskiy Inatitut.
(Oxygen) (selenium) (Sulfur)

I

PA13AUS 3 B.
KAS
in the 1603 of Wonicaddl. P,
44
- I -
-bjorme~
drolYS15 of RWUr dic A,
Ph t %mg-ka! L I PO v t t7c I j. Irm.. Kauna3, Lit
-Hydrelys'
water. ist Roetute bi i In
4.7, In _i-N IM, ind In 0.81V NinkOH. 1 21 1g,
ic 11* 81
IWOSIX41 asarmna of SL plarrd In
4peaker. and covered, with t1m. given Ii 5,; it mn~"t

tva'.
I s broken by vigormis tbaking of lbe ker,
I I)A(Ayi6 m, ))I,WMI In lqrj)~' Atagen., Scli VI [,a
-
1. 1
3(0) 1 ~ + 2110; oil)! 11t& a 1440
211
it 3 + 214,%% -116 .0, Thi

LAbst-
bezica product of hydrolyMi of SO, in mijrr ii prvdo;~InantlF,
I
C6 in dil. Rel FWn. ig identical
TISSA,

Vol WIlA OultAn "ter. u."Itolyals In uct tv buffer showed
jwnrtial Mabilizatinh of ~Illomtlfntc,: PH favor-
.
bl
l
fl
f
ifi
di
f
i
h
Ito 'imi

0. Chelmistry ea
ormat
m) O
a
tels st"miary -pact
ms
to
ul
ng
y
of thio-
tvim and ternihionatem. In - bunic mgu.~ fonvuWast
r1t, onum
Set ontlary rmratioiis it-i0v f tion
91 calloidal 8 Ano 14
W4 CW
Worie Ulf
p6lylidmile acids train rultur dic e ond thlos ate:
Ibid. IA4D-55.--Rvwtion btweeni emcd, toln, of U.&O,
obtained by Intradorink a RattL Koln. of 4N4,qX)Jtao amcd.
111CI (& 1.175). and.SCII prcYtedMftht%,)m quantitatively in
two stmge%,1_ SCI,',+ 211,0 211CI: S(010,
jisp, + -,,i fo. - li.~e oran e=cg_~ of tjdamifut6
(above the rotiti 2*0 produml SoIns; of
AdghtT. polythionie _-01014 :5),

iron (,f,W, ~Adink, hydrMill)TWL' !',ill; ;j -du. 1,f polythionie
in ang~, !rf) W-P a-
acitiq 1,
NI. 0. 11olmmt,",

YANITSKIY. I.V.; PATSAW~KASt-.X.I.
Investigation in the field of polythionic acids. Part 3. Formation of poly-
thionic acids from sulfur dichloride and thiosulfate. Zhu--.ob.khim. 23 n0-9:
1449-1455 S '53. (MMA 6:10)
1. Khunasskiy politekhnicheskiy institut. (Polythionic acids)

PATSAUSKAS-, Z.-I.[Pacauskas, E.J; YANITSKIY, I. V.Panickis, J.]
Electrohrtic oxidation of selenosulfates. Liet ak darbai no.3:195-202
161.
1. Kaunasskiy politekhnichoskiy institut.

ta 1-

875
SOURCE CODE: UR/2789/65/000/062/0097/0114
AUTHORs -Patsayeva, V. A.
ORGs
field
the free
the
TITLE: Investigation of the structure of
in
wtnd
tmosphere near frontal zones
:
OURCESI t~raV~naa ~aerqlngicheckava observatoriy_p. Trudy, no. 62,
1965. Vop ro a y L zmen ch ivo a t i ve i~r_ v t s i r k u I ya t s I I
v atmosfere (Problems of the variability of wind and other elements of
tmospher~c circulation), 97-114
:OPIC TAGS: vxete'o*'rology9 win,d field, tropospheric wind, stratospheric
ind, frontal wind structure
ABSTRACTs Results are presented for a study carried out by the Central
Aorological Observatory to determine the nesostructure of the wind
.field. The synoptic conditions included the presents of an upper-level
polar depression with a surface low moving in from the Baltic Sea, and
a jet stream and an occluded front passing over the area, The basic
data were obtained over Moscow from frequent radiosonde ascents in the
20 May-3 June 1960 period. Wind speed, temperature, and humidity
1/3

AT6008758 C>
data were plotted on a vertical (every I kim), time-wise (e7ery 2 hr)
profile and were analyzed In conjunction with weather maps. Intervals
-selected for the isotachs were I olsee, for Isogons, every 10% and
for temperature Isolines, every 10C. Supplemental, vertical, time-
wise profile# were constructed for wind speed and temperature
,measured at 1/2- and 1-min Intervals In the tropospheric layer between
the earth's ourfa.ce and a height of 3 km, This latter series of
-measurements was compared with surface weather maps, ground observa-
,-.tions, and aircraft sounding data. Wind observation-a, made with a
7- 'IMalakhIt" theodolite and by radar, had accuracies of 0-3 afsee
-:_(wInd speed) and 0-10* (wind direction). RKZ radiosonde temperature
accuracies of 20.5C In the troposphere and 'IC in the
~-stratospheree Areas of local perturbations (disturbances) extended
;_vartically not less than 1000 a and 50 km along the.horixontal., In
supplemental series of.-seasurementst the deviations in the wind
~',vpeed at the center of the disturbed areas from the averaRe speed
around the periphery were 10% of the magnitude of the velocity module
'at the center In the lower troposphere, and 15Z in the upper tropo-
Areas of localized perturbed areas were found to be charac-
'torlatic of the free atmosphere, and in them, wind speed changes
amounted to 10-15 a/sec in an hr, and around their peripheries, the
vertical wind shear attained -.values up to 15-20 u/sec per kno and
the change In wind speed with time was 10-15 a/&cc per br. The

1 21528-66
Ad NR, AT6008758
number of these perturbed areas increased with an Increase in wind
speed In the troposphere, and they were associated with the presence
r
of a surface of discontinuity In the atmosphere. They frequently
paralleled.& front and decreased in number with,distance from the
discontinuity. In the troposphere, along frontep there were 2 maxima
In ths, recurrence of perturbed areas# one in the lower troposphere
1-2 km ahead of the front& and the other in the upper troposphere
(7-8 ku under the tropopause), Orig. art. hass 4 figires and 9 tables. ER)
SUB CODEt 04/ SUBM DATE:
ATD PRZSS# IC,9,-f
&rd
none/ ORIC REFt 005/ OTH REF: 003/

ACC NR. AT6008760 SOURCE CODE: UR/2789/65/000/062/0122/0137
NUTHOR: PatsaXeva. V. A.
ORG:
TITLE: Heterogeneity of the windNIn the atmosphere and the parameters of average
notion
SOURCE: Tsentral'noya nerologicheaknya ob9arvatQ_rjyq. Trudy, no. 62, 1965. Voprosy
r-U-9-1 Wt6i'tifil ulyatsii v atmosfere
izmenchi-vosti veftal-d eleme rki (Problems of the
variability of wind and other elements of atmospheric circulation), 122-137
TOPIC TAGS: meteorology, wind gradient, atmospheric circulation, atmospheric
turbulence
ABSTRACT: Vertical, time-wise profiles of the wind field, constructed from radiosonde!
data collected'-in fifty-six 6-hr intervals in four atmospheric layers (0-4, 4-9.
9-13, and 13-17 km) were analyzed to study the structure of the inhomogeneities of
the wind under different synoptic conditions. The procedure used waa to select, by
synoptic characteristics, a number of witid perturbation (disturbance) centers in the i
wind field in a unit area of the vertical wind profile over the Moscow region. The
character of the baric field in the lowcr Lroposphere was determined from ground-level.
weather maps and that of the upper tropok;phere from 500-mb charts. The study indicatect--
that the number of short-lived perturbation centers in a wind flow with horizontal
Card I/

L 21527-U
AT6008760
dimensions of the order of tens or hundreds of kilometers and in a layer several
kilometers thick was comparatively small., given a steady average motion of Rlav - 100",
RT av, - 48. This increased to a maximum when the air flow was less steady; however,
vW it reached Riav < 70, RTav < 40, the number of perturbation centers decreased.
The main reason for this decrease was intense turbulent mixing which smoothed out
average-size perturbations. Turbulence occurred at the edges of the centers of the
perturbed areas where the gradient was greater and where, in comparatively thin layerel
the Ri and RT values were close to unity. The maximum number of these centers in the
free atmosphere occurred when the parameters of average motion (Computed for a layer
4 km thick) were as follows:
Lower Upper Stratosphere
troposphere troposphere
Velocity (m/sec) 10-15 15-25 7-15
Vertical velocity
gradient (=/sec per hr) 1-4 2-6 1-3
Riav 90 70
RTav 48 48
2/3

L 21527-66
ACC NRs AT601%
8760
In addition, in the upper troposphere in a 4-km thick layer, for a period of 6 hr or
at distances of -300 km, 5-9 centers were found which extended horizontally '
50-200 km and vertically 1-2 km. The dimensions of these centers in the lower
troposphere and in the stratosphere were half these sizes. Vie largest number were
found in the northern air flow on the back side of the lows and the front side of the
highs. Diurnally, most of the centers occurred in the daytime and evening hours.
Orig. art. has: 3 figures and 5 tables. (ER)
SUB CODE: 04/ SUBM DATE: none/ ORIG REF: oo4/ ATD PRESS: qpl,~
Card 3/3