SCIENTIFIC ABSTRACT RYKHLOVSKIY, B. - RYKOV, A.KH.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001446420007-3
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 99
• Document Creation Date: January 3, 2017
• Document Release Date: June 21, 2000
• Sequence Number: 7
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

CL

'
at
co 10' N

C;UUMOV, M.-K. K.; NARIMOV, S.; ATAZHAN'OV, M.A.; RYI9ISIKHOD4ZHIiYEV. T.
New cotton forms produced by ionizing rad3lation. Genetika no.5:
127-134 N 165. (MIRA 19: 1)
1. Sredneaziatskiy filial Vsr--soyuznogo nauchno-issledovatellskoc-o
Instituta po selektsii, genetike i semenovodstvu khlopchatnika.
Sibmitted April 28, 1965.

RYKHTER, N.V., inzhener
Method for sampling air in industrial premises for determining its
,gas and dust contents. Gig. i san. 22 no.5:73-75 Kv '57.
(MIRA 10:10)
1. Iz Molotovskoy oblastaoy sanitarno-opidemiologichaskoy stantaii.
(AIR POLLUTION,
sampling for gas & dust in indust. (Rua))

RYKHTER, E.Y.,insh.
control with Auxiliary fans in mines of the Kizel Coal Basin
Lwith summary in English]. Gig. & ann. 23 no. 3:37-44 Mr '58.
(mIRA 11:4)
1. Iz Permakoy oblastnoy sanit arno-epidemiologicheskoy stAntaii.
(DUST, prev. and control
ventilators in coal mines)
(INDUSTRIAL HYGIENE
control of dust by ventilators in coal mines)
(MINING
dust control by ventilators in coal mines)

RYMITER, E.V., inz., SHLYGINA, N.V., Idlimik
Determination of dust in the atmosphere with the electrophotocolor-
meter [with sumnary in'Engliahjo' Gig. i san- 23 no.9:18-22 S158
(MIRA 11:11)
1. Iz Permskoy oblastnoy ssnitarno-epidemiologicheskoy- stantsii.
(DUST, determe"
in atmosphere with electrophotocolorimeter (Rus))
(COWRDMSTRY
electrophotocolorimetery for determ. of duts in atmosphere
(Rus))

-RY'KHTER, E.V., inzh.
Effectiveness of 4ust elimination by ventilators operated close
to mine faces in the Kizel Coal Basin. Sbor. ra.b. po silik.,no.2:
61-70 '60. (MIRA 14:3)
1. Permskaya oblastpaya sanitarno-epidemiologicheskaya stantsiya.
(KIZEL BASIN-MINE VENTUATION)

__~YKHTERS, E.V.9 inzh.
Dust prqoij~tator of theeJection type foreatchin g coal dust.
Sbor. rabe po sAik. no.2s7:L-78 160. (MIRA 140)
1. Per-makaya oblastnaya sanitarno-epidemiologicheskaya stantsiya.
(DUST-COLLECTORS)

A- r
POLAND/Chemical Technology. - Fats and Oils. Waxes. Soaps, H .
Detergents, Flotation Agents.
Abs Jour Ref Zhur - Khimiya, No 16, 1958, 55347
Author Rykhter
Inst -1
Title An Outlook on the Industrial Development of Food Oils
from a Vegetable Origin.
Orig Pub Zycie gospod, 1956, 11, No 6, 210-21-3
Abstract No abstract.
Card 1/1

4r

r
the Pdoltalli.
iii-th-
lye, If: combli

MELINIKOV, SerM Vsevolodovichp dotsentu-RURTIKOV, Semet Potrovichi, CHAP-
SKIYI O.U., red.; BIARAKOVAq L.G., E ~e. -r, a d~,,
(Over-all mechanization of corn cultivation on the "Bollebevik" State
Farm in Lomonosov District, Leningrad Province] Opyt kmWlekanoi me-
khanizataii vozdelyvaniia kukuruzy v sovkhoze *Bdl'abevIkN; Lwono-
sovskii.Iraion Leningradekoy pblasti. Moskvap Gos.~isd-vo sellkhose
lit-ry, 1960. 60 p. (MIRA 14:7)
1. Leningradskiy sell skokhozyaystvenzWy institut (for-Mellnikol)-
2. GIavMy agronom 66*kh6zk '!Bollaheyikw'(for-Rykhtikov). 3. C ny
Leningradskogo oblastnbgo nauobno-tekbnicheskogo obabobeetTa sell-
skogo i lesnogo khozyaystva (for Mellnikov, Rykhtikov)
(Lomonosov District_-Corn (Wze)) (Agricultural machinery)

VINARSKIY. Ye.N.. inzhener; LINKOV, A.V., inzhaner; HAZING, I.V., inzhener;
CHMIkTYAITKO, V.I., inzhaner; 1YUNINAF R.L., inzhoner; CHMINA,
N.A., inzhener.'PLOTNIKUVA, M.-77.~-MIMIHF L3TPSCU, A.M., inzhener;
LELYAKOVA, L.P., inzhener; KkMIOVSXATA. M.V., inzhener; UZUIIKUTAN.
I.D.p inzhener; SEVRYWOV, Te.G., inzhoner; VINAWIT. Te.N., redaktor;
AL&DOVA, Ye.I., -takhnicheskly reaak-tor
[Metal demountable headframel Prokhodefieskie metallicheskie aborno-
razborn.ye kopx7. Moskva, ugletekhizdat, 1954.-ilo p. 092A 8:4)
1. Moscow. Yeasoyuznyy nauchno-isaledovateliskiy institut organizataii
i msk1iantzatsii shakchtnogo stroitellstva.
(Mine buildings)

SHIPILOV, Mkhail Mikhaylovich; KUZNETSOVA, Zoya Nikolayevn agr.;AMNA,,___,
Antonina Nikolayevna; KOTORA, Vasiliy Ivanovich; LE(--NOV, o.,
POKHLEBKIYA-,M., tekhn. red.
(Agronomist]Agronom. [By] M.Shipilov i dr. ~bskva, Mosk. ra-
bochii, 1962. 57 p. (MIRA 16:2)
1. Glavnyy agronom sovkhoza "Konstantinovoll Podol'skogo rayona
(for Shipilov). 2.,Kolkhoz "Bollshevik" Podollskogo, rayona (for
Ktimetsova). 3. Glavnyy agronom kolkhoza imeni Lenina Serebryano-
Prudskogo rayona (for Rykina). 4. Glamyy agronom.oporno-
pokazatellnogo sovkhoza imeni Tellmana Ramenskogo rayona (for
Kotora).
(Agriculturists)

CZECFDSLOVAKIA / Analytical Chemistry, Analysis of E
Inorganic Substances.
Abs Jour: Ref Zhur-Kh1m, No 12, 1959, 42116.
Author : Pliska., V.'-_3Y_kl1 D.
Inst : Not given.
Title Contribution.to the Polarographic Determination
of Small Quantities, of Iodine in Iodized Salt.
Orig Pub: Ceskosl. farmac., 1958,, 7., No 9, 515-5 164
Abstract: Themethod.of polarographic determination of small
quantities of iodine in iodized salt, in the pre-
sence of Cd42,eqan Internal, standard, is das cribed:
the ratio Iof'waves.of'Cd+Z and 103 when their mol-
ecular concentrations are equal is 1:3. 10 g. of
NaClJ to which I ml, of KI solution (50 mg. in I
liter of the solution) are added, and dissolved in
Card 1/2
E-14

LA N)
AdTHORS: 1) Dashcheako, 1.T., Engineor SOV/105-58-10-~21/28
%To-Am- of Uzhgorod)

Engineer 'ci6y o~ 7::zresens7-
2)
Niko1a,y,-_,, al:aya Oblast'
3) Shapiro, 1.h1. , Engineer City of L vov)
4~ Ratner, M.P., Engineer
5 Kudryashov, S.Ya., Enginet.-
6) Khaytun, E.I., Engineer
TITLE: Electric Power Engineering on a New Level (Flektroenergetiku na
novuyu stupen')
PERIODICAL: Elektrichestvc,,, 1958, Nr 10, pp 86 - 90 (USSR)
of
ABSTRACT: This is L disciisaiou/ -he artj~-le by S.M. GortLnskiy and I.A.
Syromyatnikov puolished in EleKtrichestvo, 1957,,Nr 10: 1) Even
in electrified regions, as in the Ural, in the Donbass, etc.
districts are found which are not connected with the power supply
grid. To renounce the construction of small power stations could
be of a detrimental effect. It would be most expedient to con-
struct small power stations (with a pow 'er not below 25 MW),in..,
greatly simplified power houses in a way enabling them of being
Card 113 translocated from one region to another. 2) some measures of

Electric Power Engineering on a New Level SOV/.105-58-10-21/28
rationalizing the construction, operation and distribution o-f
power in the small power field. 33 The economic expediency of sup-
plying new regions from power supply grids and of abolishing small
power stations is substantiated by a practical example from planning
work. 4) One of 'he principal reasons for the high prime coats of
small steam turbine power stations is a mechanical transposition of
the principal engineering schemes and of -the design of large -Dower
stations to small-scale ones. More up-to-date principles off Im-
proving the ope-rai-ion factors of such stations are advanced Etnd 3
conversion-from a sclid fuel to a liquid or,gas fuel opera-.-!on IS
requested. By the latter measure a complete automation of steam tur-
bine power stations will be made possible. 5) Experience gained in
the enterprises of the Gla-;elektromontazh demonstrated that the
time has come to introduce an industrialized method of aas=_M'61,-,r.
Each electrical equipment should be designed as one great b1c.-k of
equipment, weights reaching 2.5 t. 6) Insufficiencies and shor-,
comings in electrical industry are pointed out. A number of cases
are mentioned, where it was impossible to obtain apparatus and
parts of equipment which had been developed already a long time,
Card 2/3 ago. There are I figure and 2 tables.

Electric Power Engineering on a New Level SOV/105-58-10-21/28
ASSOCIATION: 4) Transelektroproyekt
5) and 6) Ifuybyshevskoye otdeleniye F.Lektroproyekta (Kuybyshev
Branch of the Elektroproyekt
Card 3/3

DASHCHWNKO, I.T.,inzh. (Uzhgorod);-4Y]%XN F.G.,inzh. (Voznese nek, Nikolayevokoy
oblasti); SHAPIRO. I.M..,inzh. (L'vovT; RATNER, M.P.,inzh.; KUDRYASHOV,
S.Ya.,inzh.; KHAYTIRI, B.I.,inzh.
Power systems at a new level. Blektrichestvo no.10:86-90
0 158. (MIRA. 12: 1)
1. Tr--nseletroproyekt (for Ratner). 2. Kuybyshevskoye otdeleniye
Blektroproyekta (for Kudryashov, Khaytun).
(Electric power)

RYKLIN, F.G., inz-h.
f7-
Electric motor drives for oil switches. glek.sta.
31 no-5:41-44 My 160. (MIR& 13:8)
(Electric driving) (Blectric cutouts)

AID P 4103
Subject USSR/Electricity
Card 1/1 Pub. 27 - 14/24
Author Ryklin, F. G., Eng.
Title Operation of fus.es of the FK type In outdoor installa-
tions.
Periodical Elektrichestvo, 11, 75-76, N 1955
Abstract The author discusses the use and operation.of fuses
of the PK type in outdoor,installations. He is of
the opinion that fuses of.this type are well adapted
for operation in zones of industrial contamination
as well as outside them, and in Ivertical as well as in
horizontal position. The author gives some technical
data obtained from tests. One table, 2 photographs.
Institution None
Submitted N 30, 1954

-- -- - -- - I --- ---
RYKLI1T, G.
Ikeounters. Izobr.i rats. no.2:40-43 F '60. (MIRA 13:8)
(Technological innovations)
iii

2. USSF (60'~)
4. Carter, ~~;eribert Dyson, 1910-
7. Dollar n-1presslon ("The future in our favor." Dyson Carter. Re.viewed G.
Zykliln), "~Lulhi zllizml,!~
no. 1953.
9 Monthl List of Russian Accessions, Library of Congress, I-lay -1953, Uncl.

"Y'-'T T1,12y
Ll-f- in a '~azn ve n ttranclEtel"', f-= E-Ell--Ih-)
in Nal,ka i z'~nizn I l') no
J 2
Accesc-ons, Library of Congress, Deceraber 19!:2.

AiD P 61o
Subject USSR/Electricity
Card 1/1 Pub. 27 - 14/35
Author : Ryklin, F. G., Eng.
Title : Automatic synchronization of generators without control-
ling frequency
Periodical Elektrichestvo, 8, 64-65, Ag 1954
Abstract This simplified method is used for low-capacity generators
(Diesel-generators, etc.), and permits reducing the start-
ing apparatus as well as the operating personnel.
Institution Not given
Submitted Ap 6, 1954

EREZ, S.L.; RYKLMA, A.G.; BOMAREV, A.S.
Clinical characteristics of nonspecific ulcerous colitis.
Kaz. med. zhur. no.1:19-22 Ja-F t62. (VIRA 15:3)
1. Kafedra in fektsionnykh bolezney (zav. - dotsent.
S.'L. Erez) Donetskogo meditsinskago instituta i oblastnaya:
boll.nitsa imehi M.I. Kalinina (glaynyy vrach D.A. Shparenko).
(COLITIS)
(ULCERS)

I S I he I I U It OR It -is 17 a 'to a it n IS Jd J, a
A A-L r It T x; is J; UIRSISumme it a a
.3 Olt .-M (X M-EK
00
00 .00
Proplimi"A hufural from flax fjow. N- N. 01 I..v A -so
J- A MW Chosen, W. Ii. S
00 I(Ilik - R.) 0.
as To"Mmall 6 twat 4AAdutoll Itum 114% low 1"11,111K
I- In with oill 0111111itt. of MOO 19,17. 411,1~1 o00
00 1*11 IWI and NaVI. 'r%e ItAinoititt
am VISM"Ifiell IK'%'t)ldb
as 3 111 lu thVir vI1k'kWv' , IWI
00 1 1 .,act (4%)Iaftd flao 12.8%). A41dn. of NaCI ago
14, ills- Will %Wsm, not nc"4LW the yield fit fliffural toil it
so Ikatt,ttl live little mquired fin, ihor tr~tt.m b 1114116
I I.-'t,Ouwn, fw im Witt, ark-i'tding 14) 14h. r%ismi I, is I goo
.%-. V44tilia for 7-7.6 hill. 6 requkvd with avid almii, list '100
I a :t 4 Itr%. with eM and satt. The urating tr,%Ot,. I,
00 1.%S 1W sit I; aim. prt~.atr. It iti mst I-ilj,- t,o eattmen
st"d (tarfistal A~ A. 144~hthnjlk
oo7v zoo
ago
AL It I ~j. tj IS'
-5-11- v it. -
v
9 a IV n It a Of a a a 0 PI a ft 1( a MW A Altai
f 0 0 0

Rynis , S. C'.
"Kinetics of the Reaction of Forruition of Ort-ho- and Para-Nitro-anisol from
Ortbo- and Para-Nitrochlorbenzene" (p. 1515)
SO: Journal of General qhem:~!j ~r, (ZhiLrnal Obshchei Khimii), 1247 ol. 17, No.

=S S G' Go 0

~T 17: dhiifiil) Abet o"tkows

"
--
a p Momo Z.JW.

RUSN%n effect.
r

-
,46b~'~l 954
0 1
'
,
Thv Wt'
t:'
t
ei
lt
btif
v
d
I
dW
1't
A',g;.lwrganld Chemistry ru
u
.
s we
e
o
ne
was
n
a
s
r
.&A.-w*-wlkh33 tiom Br,.wheii 75% crude 50
or
'
'
i
d
uct W
tte a ed
G.
pm

N.

VEWWAN. R.F. RYKLIS. S.G.
Synthesis of 2-aminomethylbenzothiazoles by the cyclization of
ryl -tolyl-thioureas.Ukr.khim.zhur. 20 no.1*73-76 154. (MLRA 7:3)
1. Ukrainakiy nauchno-iseledovatellskiy institut tuberkalaza.
(Benzothiazole) (Thiourea)

KUL'BERG, L.M. Edeceai3edl; RYKLIS, S.G.; YUFA, P.A.; VBL'TM&N, R.P.
Synthesis and properties of sulfametine, the new antitubercular
preparation. Zhur.ob.khim. 26 no.1:168-172 Ja '56. (MLRA 9:5)
1. Xhimicheakays laboratoriya Ukrainskogo nauchno-insledovatel'-
skogo instituta tuberkuleza, Kiyev.
(SULTANITINE) (TUENRCULOSIS)

5(3) PHASE I BOOK EXPLOITATION SOV/1409
Ryklis, Semen Girgorlyevich, and Mariya Pavlovna Vysotskaya
Laboratornoye rukovodstvo po sintezu promezh,-,tochhykh produktov i
krasiteley kLaboratory Manual for the Synthesis of Dyes and.In-
termediate Products) (KIyev] Izd-vo Kiyevskogo unIv-ta, 1958.
191 P. 5,000 copies printed.
Ed.: M.S. Gornostaypollskaya; Tech. Ed.: T.I. Khokhanovskaya
PURPOSE: This laboratory manual was approved by the Ministry of Higher
Education of the UkrSSr as a textbook for chemical engineering de-
partments of vuzes In the UkrSSR. It is intended for students.spect-
alizing in the technology of organic dyes and intermediates. It may
also be useful in textile vuzes.
COVERAGE: The text of th15 manual isbased on the program of the Lab-
oratonj of Organic Dyes designed for 4th and 5th year students at
the f1dyev Polytechnical Instlt!ite. The f1rnt part 18 devoted to
dye intermediates. The subject matter lo arranged according to the
program of the course on "The Chemistry and Technology of Intermed-
iates." The problems included in the first part deal with the syn-
Card 1/11

Laboratory Manual (Cont.) SOV/1409
thesis of dye intermediates. The second part covers dyes and com-
piles with the program of the course on ff-The Chemistry and Techna-
logy of Dyes." Problems for both parts were composed on the basis
of patents, literature sources, research papers, and experimental
work of students, and were tested over a period of several years
at the Laboratory of Organic Dyes at the Kiyev Polytechnical Insti-
tute In practical assignments for students specializing in the tech-
nology of dye intermediates and dyes. There are 20 figures and 13
references, 12 of which are Soviet. No personalities are mentioned.
TABLE OF CONTENTS:
Preface 3
PART 1. INTERMEDIATES
Sulfonation
.1. Calculations for the preparation of sulfuric acid solutions 7
2. Sodium benzenesulfonate 9
3. 1,3-Nitrobenzenesulfonic acid 11
4. 4-Nitrotoluene-2-sulfobic acid 12
Card 2/11

Laboratory Manual (Cont.) SOV/1409
5. Sodium 2-naphthalenesulfonia acid 12

6. htholdisulfonic acid
2,6-naphthoisulfonic acid and 2,3,6-na
14
7. 2-Naphthol-6,8-disulfonic acid (G acid
~ 15
8. 1-Anthraquinonesulfonic acid (potassium salt) 16
9. 2-Anthraquinonesulfonic acid 1.6
10. Sulfanilic acid 17
11. Naphthionic acid 18
Nitration and NitroBation
12. Calculations for the preparation of the nitrating mixture 18
13. 1,3-Dinitrobenzene 22
14. 2,4-Dinitrochlorobenzene from chlorobenzene 24
~15. -o-Nitroacetanilide 24
16. p-Nitrcaniline 25
1
- 3-Nitro-.4-toluldine 26
~
1 . 1-Nitronaphthalene 26.
19. 1,5-and 1,8-dinitronaphthalene 27
1-Nitrosophenol 28
21. 1,2-Nitrosonaphthol 28
22. 4-Nitrosodimethylanilinechlorohydrate 29
Card 3/ 11

Laboratory Manual (Cont.) SOV/1409
Chlorination
23. Chlorobenzene 30,
24. Benzylidene chloride -31
25. 1-Chloroanthraquinone 32
Reduc tion
26. m-Phenylenediamine 33
27. Methanilic acid 34
28. (x-Naphthylamine 34
29. o-Anisidine 36
30. m-Nitroani..--qne 36
31. Benzidine from nitrobenzene 37
32. 1-Amino-2-naphthol-4-sulfonic acid 4o,
Subst itution of a Sulfc azy-iAmino Group with a Hydroxyl Group
33. Phenol from sodium benzenesulfonate 41
34. P-Naphthol 42
35. 1-Naphthol from 1-naphthylamine 43
36. 1-Naphthol-4-sulfonic acid from naphthionic acid (Nevile-
Winther acid) 43
Card 4/ 11

Laboratory Manual (Cont.) sov/14og
Replacement of Chlorine With Other Substituents
37. 2,4-Dinitrophenol from 2,4-dinitrochlorobenzene 45
38. Benzaldehyde from benzylidine chloride 45
39. 4-Nitroanisole from 4-nitrochlorobenzene 46
40. 2-Nitroanisole from 2-nitrochlorobenzene 47
Diazotization and Diazo-group, Conversion
41. Phenylhydrazine-p-sulfonle acid from sulfanilic acid 48
42. Thiosalicylic acid 49
43. 3-Nitrotoluene 51
44. 1.,3-Chloronitrobenzene 52
Acylation
45 Acetanilide 53
46: Acet-p-toluidide 54
47. Anillde-2,3-oxynaphthoic acid (azotol A) 55
48. Acetylsalicylic acid (aspirin) 57
49. Phenylsalicylate (salol) 58
Card 5/ 11

Laboratory Manual (Cont.) SOV/1409
Alkylation and Ar.~unination

50.
Phenylglycine-o-carboxylic acid 59

51.
Phenylthioglycol-o-carboxylic acid 6o
52. Di henylamine 6o
53. 2,&-Dinitro-41-oxvdiphenylamine 61
54. Phenylperi acid 62
Oxidation
55. Anthranilic acid from o-acetotoluidide 63
~56. 4-NItrobenzoic acid 65
57. Anthraquinone from anthracene 66
58. Anthranilic acid from phthalic anhydride 67
Condensation and Cyclization
59. Synthetic anthraquinone 68
60. 2-Chloroanthraquinone 70
61. 2-Methylanthraquinone 72
62. Benzanthrone 73
63. 8-Oxyquinoline 74
64. 1-(p-Sulfophenyl)-3-methyl-5-pyrazolone 75
Card 6/ 11
-----------

Laboratory Manual. (Cont.) SOV/1409
aration of Complex Intermediates
Pre
g
5.
1-Naphthylamine-5-sulfonle acid.and ne-8-sulfo-
1-naphthyla
mi

nic acid I
76
66. I-Naphthylamine-6-sulfonic acid and 1-naphthylamine-7-sulfo-
nic acid (Cleve acids
V 78
67. 1-Amlno-8-naphthol.-
disulfonic acid (H acid) 79
68. Diaminostilbenedisulfonle acid 83
PART 2. DYES
Nitro and Nitroso Dyes
69. Naphthol, yellow 87
70. Fast Yellow 2K 88
71. Mordant green Bs 88
.72. Pigment green 89
Azo Dyes
73. Mordant yellow go
74. Acid metanil yellow 91
75. Chrysoidine 93
Card 7/ 11

Laboratory Manual (Cont.) SOV/1409
76. Oil orange 94
77. Acid orange
78. Acid scarlet 96
79. Acid brilliant red 97
80. Acid red S 99
81. Acid red Zh 100
82. Acid red 2S 101
83. Acid bordeaux 102
Acid blue 2K 1o4
85. Light-fast acid yellow 105
86. Acid chrome blue black 1o6
87. Acid chrome red 107
88. Acid blue black log
89. Oil darkred 110
90. Acid red 2Zh 122
91. Acid blue K 114
Acid black S 117
93. Basic brow-h 119
94. Congo red 120
95. Direct blue K 121
96. Direct violet 122
Card 8A1

Laboratory Manual (Cont.) SOV/1409
97. Direct brown KKh 124
98. Direct yellow ZhKh 126
99. Direct red Kh 127
100. Direct bordeaux 129
101. Direct brown ZW~h 131
102. Direct green
103. Direct green ZhKh -135
104. Direct black Z, 137
105. Direct light-fast blue 140
106. Brilliant yellow 1,44
Di- and Triarylmethane Dyes
107. Auramine 145
108. Malachite green 146
'
109. Basic brilliant green 148
~110. Acid brilliant blue 149
111. Parafuchsin 152
112. Basic violet K 153
Card 9/11

Laboratory Manual (Cont.) SOV/1409
Xanthene Dyes
113. Fluorescein 154
114. Eosine 155
115. Rhodamine S 157
Quinonimine Dyes
116. Basic dark blue 2K 158
117. Methylene blue 159
118. Safranine T 161
119. Induline 163
-120. Nigrosine 164
Sulfur Dyes
121. Sulfur black 165
122. Sulfur blue 165
123. Navy blue 166
124. Immedial black 167
Oxyketone Dyes
125. Alizarine red 168
126. Alizarine red from P-chloroanthraquinone 169
Card 10/11

Laboratory Manual (Cont.) sov/1409
127. Alizarine brown (anthragallol-1,2,3,-trioxyanthraquinone) 170
128. Alizarine blue Bs
129. Acid alizarine red S
Vat Dyes (Indigo and Polycycloketone Dyes)
130. Indigo blue 175
131. Thioindigo red S 176
132. Thio1ndigo scarlet Zh 177
133. Vat dark blue 0 178
134. Vat blue 0 180
135. Vat golden yellow ZW~h 181
Bibliography 183
Subject Index 184
AVAILABLE: Library of Congress
Tm/sfm
5-6-59
~Card 11/11

RULTS, S.G.; SJUI-N, S.M.
r3-obtinuoua-procoss condnnoation of chloral with chlorobonvene.
Zhur. prikl.khim. 31 no.7:1114-1118 JI 158. (MIRA. 11:9)
1. Kafndra or,,-anicheslcogo sintoza Kiyovskogo ordena, Lenina.
politeklinicheskogo instituta.
(Condensation producta (Chemistry)) (Cbloral) (Benzene)

RYKLIS Semen Grigorlyevich; VTSOTSKAU, Marlys, Favlovna; GCRNOSTAYFMISKA.U.
T,,I*, tekhn. red.
Claborator7 manual for the synthesis of dyes and intermediate
1productal Iaboratornoe rukovodstvo po sintezu. promez'hutochnykh
produktav i lcr6iitelei, [Kievil Izd-vo Kievskago gos. univ. im~
T.Gl Shevchenko, 1958. 191 pe (KIRA 11:10)
(Phint) (Dyes and dyeing)

RUBAN, Ye.L.; RYLKIN, S,.S.; POKROVSK.AYA, N.V.
Relation of Hitrosomonas to radioactive saccharose and carbonates
[with summary in English]. Mikrobiologlia, 26 no-3:257-262 My-Je 157.
(MIRA 10:10)
1. Institut mikrobiologil All SSSR, Moskva.
(NITROSOMONAS. metabiolism,
carbon, determ, labeled sucrose & carbonate (-Rua))
(SUCROSE, metabolism,
Nitrosoponas. radioisotope-labeleci in determ. of
carbon metab. (Rua))
(GARBON, metabolism,
Nitrosomonss, determ. with radioisotope-labeled sucrose
& carbonate (Rua))

ihe
I

RYKOWSKI, H.; P.I?ASZAWWICZ, B.; KAZIMIXRGZAK, J.; PANAS3WICZ, J.; HUBL, S.
:,bmerlmental af3aay with control of ventricular fibrillation in bloodless
heart aurgery In kypothermia. Acta nbysiol. polon. 19 no-3:515-5~7 1957.
1. Z Il Zakladu Chirurgii Instytutu Doskonalenia I Specjalizacji Kadr
Iekarskich Kierownik: prof. dr J. Rutkowski 2 Kliniki Chirurgicznej
Instytutu Hem-atologii Kierownik: doc. dr A. Trojanowski Z Zakladu
Fizjopatologii lnstytutu Hematologii Kierownlk: kand. nauk ined. J. Pan-
asewicz Prace wykonano w ramach tematyki Komisji Patogenezy Wstrzasow
Polsiciej Akademii Nauk.
(HYPOTMMIA, experimental,
in heart surg., prev. of ventric. fibril. (Pol))
surgery,
exper. bloodless with hypothermia, prev. of ventric. fibril.
(P01))
(UNTRIGUIAlt FIBRILIATIOIT, prevention and control,
in exper. heart surg. with hypothermia (?o1))

RYKOV, A.
Sotsialisticheakaia rekonstruktsiia sviazi,vo vtorom piatiletii. &/Socialist recon-
struction of the communication system in the second five-year plan/.. (Planovoe
khoz-vo, 1934, no. 1, p. 182-199).,
1. General results of the first five-year plan in 1933.,
2. The main trend of the second five-year plan.
3.. The main tasks of reconstruction of,communications.
4. Development of the main radio communication network.
5. Telegraph apparatus.
6. Interurban stations.
7. Regional electric communications.
S. Gity telephone system.
~9. Radiobroadeasting, radi.ofication and television.
10. Reconstruction of postal service
DLC: HC331-P52
SO: SOVIET L4NSPORTATION AND C0101UNICATIO A BIBLIOGRAPHY, Library of Congress
Reference-Department, Washington,.1952,-Unclassified..

R A.
(-.-snav~iye zadacki:7. sviazi.. -1e main tasil-5 01, commicatic -7. (Planovoe 1,.-Ioz-vo,
-,,ic new ttltgrapa and interLx'E)zn tele,,honc lines
iJ35., no. 2, 12-6-135'
k;;. 126). AG HC331.P,52
3C:. Sovict lrans'~ortw~auviun and Gommunjxat~
icps, A61blicL~rap-cV, UbT~~,y_of Congress,
Reference i)epartment, ~Tasldngtcn, 19152, Unclassified.

r
IL?KCV, A.
Oznovn~c zaaacid L/Ililc -6-in oroblcir3 of comamication2s. (Planovot k.,cz-70.,
i93c, nc. 2. p. 126-135 The new teitgraph lines, t" 1,7 nterurban teL- pnone.
lincs (1). 126). DLC: HG331.P52
SG: Soviet Iransportatim And Gommmications, 1.jib -do,,rajji* Library cf Congress,
~-.Ten-ce Department, lolaspington. 1952, Uncla!:sified.

RYKOVY A. G. SPITSYN, V. I., SAVICHY I. A., and PIKAYEV, A. K.
tic
ompiex Compounds of Hexavalent Uranium :With- Some Organic
Substances; Paxt 2-- Inner-Complex Salts of the Uranyl Ion
With Snm Derivatives of 2-Naphthol and of 1,2-NaphthoqLinme~'
by I. A. Savich, A. K. Pikayev, A. G. Rykov, and V. I. Ut*n'
Mscow State- Univer sity, Zhurnal Neorganicheskoy Khimii Vol
1, No 19, Dec 56,,' pp 2742--2-7lF5-
According to the article, comp3unds of the uranyl ion with 3-bromo-
-1,2-naphthoqu-inonemonoxime-I and 3,4-dichloro-1,2-naphthoquinone-mon-
oxime-1 were obtained. It was established that the compound of 3-bromq-':..
l,2-nqpbthoquinonemonoxiAe-1 vlt'a uranyl forms crystalline solvates with
,water r7,
and alcohol. The solubility~of these solvates in water was dete
miAed..
Sum 1258

RYKOV, A. G., SPITS)M, V. I., SAVICH, I. A., and PIKAYEV, A. K.
a,=. Inth':
"Complex Compounds of Hexa~r&lent,
Substances;:Part 3 -- Precipitp-tion of Uranium Proir, Aqueous
Solutions by Mesns of Some Substances Related to 3--Nitroso-2-
Naphthol, " by I - A - S avich, A - K. Pikayev, A - G Rykov, and
V. I. Spitsyn, Ybacow State University, Zhurnal Neorganiches-
koy i, Vol 1, No 12.? Dee 56,.pp 2746-2748
It has been established that 3-bromo-1,2-naphthoqui-nonL-m n xime-l
can be used as a precipitant for uranium. The precipitation of uranium
with this reagent is complete and takes place at pH - 2-7. It has
furthermore been establ-A'shed. that 3,1~-dicbl-oro-1,2-naphthoquinonemonoxime-1:
cannot be used as a reagent for the precipitation of uranium.

ZAYTSFV, A. A., KOSYAKOV, V.11., RYKOV, SOB010V Yu Y. an(T-Y17UKOVLLV, ic-- IT
(Inst of Atomic Diergy AS USSR)
"Lmiestigantion of Several Oxcidation-Reduction Reactions of An-ericium"
Isotopes and Radiation in Cbemistry, Collection of papers of
2nd A3.1-Union Sci. Tecb. Conf. on Use of Radioactive and Stable Isotopes and
Radiation in National EconorW and Science, Moocov, Izd-vo AN 530, 1958, 3&)PP-
This mlume published the reports of-the Chemistry Section ofthe
2nd AU Sci Tech Conf on Use of Radioactive and Stable Isotopes and Radiation
in Science and the National Economy, sponsored by Acad Sci USSR and M3jz
Admin for Utilization of Atomic Energy under Council of Mmisters IMSR
~bscow 4-12 Apr 1957.

5 (2)
AUTHORS: Zaytsc-v, A. A.o Kosyqk.-)v, V. 30V/89- 1-! --7/,6
_Ry~,-f-A. '-L;.g- Sobr)ltmr-, Yu. P.,
Yakovlev, G. N.
TITLE: The Radioly-l-lic Red'o.-tior. of A~z ('VI', an.d Am (Y)
skcyc vssstanorlew..,re Am (V Am ('V))
PERIODICAL: Atrmnaya mergiya, 1.959, V~~-" '7, Nr 1, pp 37 46 (USSR)

ABST RACT:
-bants c.-,f the radi
The cons
~:ly-'-1-
--ea rzl-~.e u.0-- P-
of A
---y
. -
)
d
hl
i c---
,3
T,
0r
da-
kc:nmlned, the t.he xl~lld-C.7,1.:n yz..,~~du,-.ts f=-
ni~ihing the val,ues f-Or the m-eaction rato. If these
quantities arecomb--ned rith th-) cf liydn;ger,. -pe-r-,
oxide. -4t is p~~-z-sibl? hsEm%if.-m tl-c- ~~.y 4-_-,,
contrila,--t-.17op. made -i%y "alydrl-ogen nsdi~-alz ir, th-D Tdluc~6ic,
n
-'lior. . ou th-c-1 C; dat7i --" t is b:?~ �,,~;ve.-d. t,---
pr)SSitjj- 4-0
M.- - rjj:~M ff:;r flii -rad--*.oly'li:;
2+
4.-he
Airt01? a n. dAm 02
rat e ol AmO i i.s ";,h,--; -~z hy..
Card 1/3, drLFsn per~,Yild,--, ar.0. c...f hyd..---:U,~~r, in the

The Radiolyti,~ IteducLifin if A.~a (111) P"S (V)
0 %tea Tho fo I! ~,-iI - s t b,~ I wi
to '-h eex-
24'i
Parimante-I part: Cherdnally x a s .z-, na J.
nel '._"_~Is 'haa Th~ t4irmu,-al Jrz-
ag; rictlum in 4'a-
ticn:i r.3rE
measui~-s'4.. The --.-? -the
cf A-110) and A--k/VI), ard th~,- I,--.I:::xmu'LEit-J.~,_n -:f hydx~~gen-
241
- - -; c 1 1.1. The
in. Am a-,Auldons ~4,z'-t r i t z..:! i - r. d z ~ _.
ed are partly o_'iown by ~~.-.J. th~_- fijll~;wing !~-_-u-ve,3
3 tA.
special P-) ra;i 4.%. 2:, z; S: 7. q f vu- j. -I im i n
2.0 M IICIO an,
.1 0. ~: I'l H_:~ 11-1 1.1 J,4."SD' I r Ij.,~J.yLj
n a_ c; n:
-4 '_ 41
ac t I on !.~ f L(V) i a t ior: H, 0 in 1.9 1', H S
4
2
.
riation of t"-ne., sv-.%~.13-_ tate (Y) f sm,2.ri in -~h~~
radiol~rti~; J.n 9.0 M HCIG, ai, va_-!.~uzz
C' rz~ V_ X, a '..J. C, r_ s .C.- :Df
V.
~n t1w. :--adi-n"ytic n 0-5 M H N C, D
t
14.13 M IMO.,. Th, d the Y4,7-1_1- tlh~:.
s o~~, :lyt
Card 2/3

Olyt4C -7/26
The Radi Reduction uf Am (VI) and km (V) SOV/BC-7---? 1
tion of AmOr- -'-, the c-baervprl 2nd -:-alculatE.J relunti-nn ra-i-a Cf
I + 2
AmO2 in 0. ? M IH2SO4, a's Well as~ the Yields, of H201:) an-1 of thG
hydrogcm radicals irt hydro:1hlo2,i,-.-. a-:;iii are g-11-1-r.
in tables. Theva ar~~ 7 figures, 3 tablevo a-zill 13; -i~ferani:;P.8,3
of which ara Soviet,
SUBMITTED: Nmrember '17, 19.59
Card 313

'21 (1), 5 (2)
AIN HORS: luaytsev, A, A., XI-osye-k-ov, V. N., SOVI/89-7-1-1-3/26
A. G. Sobolev, Yu. P~' Ya~covlevj G.
TITLE: Dispro-portionation of Am (IV) (Dis-,roportsionirovaniye Am,(IV))
PERIODICAL: Atomnaya energiya.. 1959: Vol 7, lk- 1, PP C-59-711 ( US 11) R)
ABSTRACT: As a preliminary result, it is said that the -.reactions
2Am414 + 2H 0 Am 34- + 1~ma+ + -411 4- and
A + 2
+ 2+ h
Am't + AmO Am + A_-O have actually been experimentally
2 2
proved. The production of the various chemical sc-lutions and
the times needed for working~up the material ar .e given. The
0
concentration of Am (III), Am (IV), and Am (VI) was measured
by means of the quartz spectrometer SP-4. The material to be
measured was filled into a hermeti3ally closable cylindrical
euvette of 2 cm length, and was j-,Leasured in the spectrometer in
this condition. Total americium concentration was determined
241 Apart from Ithe initially
from the w--activity of -the iLm
mentioned results, it was further stated that.-the reactions,
3+ 2+ +
Card 1/2 31 Am4+ + 211 20 2 + AmO *2 + 4H

Disproportionation cf.La ~IV) sov/e,9-7-1-13/26
2AmO-i- + 4H + = AmO 2+ + Am4+ + 2H 0 can be Droved. The yields of
2 2 2
individual reactionc ny, a-,Kn Lhe molar concentration,
of the various solutions are mentioned. There are 1 table ani
8 references,:2 of which are Soviet.
SUBMITTE-D: November 17, 1958
Card 2/2

ZAYTSEVJ, A.A.; KOSYAKOIT, V.N.; MYTOIT, A.G.; SOBOIZV, Yu.P.;
YAKOVIZV, G.N.
[Kinetics of americium (V) reduction by hydrogen peroxide]
Kinetika vosstanovleniia ameritsiia (V) pereldsliu vodoroda.
Moskva, In-t atomnoi energii 21 SSSi, 1960. 11 p.
MIRA 16:12)
(Americium) (Reduction, Ghemical)

ZAYTSEV., A.A.; KOSYAKOV, V.N.;_EffOV,-A..G.; SOBOISV, Yu.P.;
YAKOVIEV, G.P.
(Disproportionation of americium (V)] Disproportsioniro-
vanie aneritsiia (V). Moskva, In-t atomnoi energii All SSSR'
1960. 18 p. (MIRA 16:12)
(Americium)

gwp(j) Awp(t) Ir-TT .7 /t'1Tw/Tr'F/1n4RM
ffr E 1/070r/
~'fl M[0166/66[0 0049
AUTdOR: Rykov, A. G.; VaBillyev, V. Tao; Yakovlev, G. N.
ORG: none
TITL-',: Investigations of oxidation-reduction reactions of actinide elements. III.
rdnotics of,tho reaction beUTeen uranium (IV) and bromate ions in perchlorate solutions
SOURC&: Radiold-iimiva, v. 8, no. 1, 1966, 33-42
TOPIC TAGS: oxidation reduction reaction, chemical !dnotics, uranium, bromate, anion
stoichiomotry, roaction rate, hydroGen ion, ion concentration
A-303T.'UCT: The mechanism or the conversion of 141;* ions to
~102 or M03
ions in the reaction with anion oxidants has not been wall sttidied. The
present study deals with the kinetics of oxidation-reduction reactions of
ions of actinide elements with oxygen-containing anions. The experiments
on the determination of the ntoichiometry of the reaction were conducted
,at 25oG in 2 M"C104 ~ The results showed that the stoi:chiometric coefficient
of thereaction remdins approximately constant within the limits of 2#1-2-3
with a change in the ratio of initial reagent concentrations ARIVId -L
ffirQ5,7. from 2-5 to 5-5- Evidently, the principal reacTolon is
Zj4+ B - + 2H20 2UD&+ Brd- 4. 4H4
roj 2
UDC.- 541*127+546*79194

L 34051-66
ACC NR: AF6025486
accompanied by considerably slower oxidation of U(IV) by Bro- ionse..
It has been shown that the reaction governing the rate of the overall
process passes through two activated complexes formed under different
equations. The reaction rate in the first route does not depend on con-
centration of hydrogen ions, and along the second - it is proportional.
to the square of the H+ ion concentration. Thermod~mamic value3 have
been found characterizing the reactions, of formation of each activated
complex. The formal entropy vplues of these complexes have been caicula"!k-"
Orig. art* has:. 10 figures arj,7 tables. Li'lits: 35,728-7
SUB CODE: 07. SUM DATE: 23Nov64 ORIG REFt 010 OTH REM OU
Card2

L b035o-66 E;a (j ) /E~.Yr (M) /n,,p (t) /ETI IJF(c) R1,1Aj'TX,/JW/JD/JG
ACC NR. AP6019151 (A SOURCE CODE: UR/0186/~6/008/001/0020/0026
~AGTHOR: Rykov, A. G.; Yakovlev, G. N.
ORG: none
!TITIS: Study of redox reactions of actinide elements. Part 1: Kinetics of the reac-
Ition between ne-otunium (IV) and neptunium (111) in perchlorate solutions
44,
SOURCE: Radiokhimiya, v. 8, no. 1, 1966, 20-26
TOPIC TAGS: naptunium, oxidation reduction reaction, oxidation kinetics, perchlorate
ABSTRACT: The kinetics of the reaction between N-D(IV) and No(VI) ions were studied in
perchlorate solutions with an ionic strength of 2.0. Spectrophotometric determination
of the concentrations of No (IV), (V), and (VI) showed that the stoichiometric rea ction
is given by the equation
'.~(Iv) + NOM) 2 NDM.
soect to both I
The reaction is first order,with-re Np(IV) and N'p(VI)
d [,NP([N')]
dt- k' [N p('V)j 1--4p'"].
A study of the reaction rate as a function of acidity and terip erature was made.
Since the reaction can proceed along several (at least two) parallel paths, the follow-
Card 1/2 UDC: 541.127+54-6.799.3

L 40350-66
ACC NR: Ap601915j
ing reaction mechanism is propose.d
INP4++ NPo21- +11,0 211+,
2
k,
k,
NP4+ + NP021 +2 ff'o (*)31,+ 3 If
2
k3
-:!I Pr-JLc4j
where stands for an activated cormlex. of charge' +n. The corre sponding reaction
rate constants were found. The thermodyna c quantities characterizing the process of
formation of both activated complexes were obtained, and values of their formal entro-
-pa.esiwere calculated. Orig. art. has: 3 figures, 3 tables, and 15 formaas-
SUB CODE: 07/ SUBW DATE: 07Sep64/ ORIG REF: 002/ OTH REF: 021
Card 2/2

IJP(c) RYI',T,,'IJDIJG
L 403h01-66 Et-.-T (j /M-,T W /EWT W AT I
ACC NR: SOURCE CODE: UR/0186/66/008/001/0027/0032
AP6019152 Z, A)
AUTHOi: 1~,kov, A. G.; Yakovlev, G. N.
ORG, none
TITLE: Studies of redox reactions of actinide elements. Part 2: Kinetics of the re-
action betureen ner-tunium (IV) and neptunium (VI) in nitrate solutions
SOURCE: Radiokhimiya, v. 966, 27-32
no.
TOPIC TAGS: neptunium, oxidation reduction reaction, nitrate, oxidation kinetics
ABSTRACT: The effect of complexing of No(IV) and Np(VI) with nitrate ions on the ki-
notics of the stoichiometric reaction + 1,.'D(V.L) - 2 No was investigated at an
ionic strength of 2.0. The reaction is first order with respect to both Np(IV) and
No (VI) j [Np('V)l t d [Npl"]
dt dt
In the presence of nitrate ions, the reaction passes through two activated_~ ~lexesj
02+
Np4++Np 2 + n1120 Z= (*)+07 + M11+1
0+,,,,o
++,qpo2l,+n[12 3
'4P4 2
,(where stands for the activated comolex) which then decomoose via independent athsl
p
Card 1/2 UDC: 541,127+546,799-3

L 40349-66
ACC NRt Ap6()19152
7he main path of the reaction involves the fornation of an active cormlex whose compo-
sition includes only one NC~-ion. The thermodynamic quantities ( AH*, aG*, as*, S*)
characterizina- the formation of the nitrate activated comDlex were calculated. Orig.
0
art. has: 2 figures, 3 tables, and 16 formulas.
SUB COIZ: 07/ SUBM DATE: 07Sep64/ OKG FEF: 001/ O-IH MF; oo6
Card 2/2