SCIENTIFIC ABSTRACT BOLDYREV, A.M. - BOLDYREV, I. V.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R000206110014-6
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: June 9, 2000
• Sequence Number: 14
• Publication Date: December 31, 1967
• Content Type: SCIENCEAB

T ?1418-6~ T'3p
ACC NR- AP6008811" SOURCE CODE: UR/Ol 5 66/ooo/003/0002/0006''
AUTHOR: Nikiforov, G. D-1. (Doctor of technical sciences); Boldyrev, A.Ma~
-Bukurov, V. I .
ngineer (Engineer)
ORG: MATI
TITLE: The mechanism of porosity formation and the effect of some
:welding conditions on the porosity in AMg6,41loy welds
SOURCE: Svarochnoye proizvodstvo, no. 3, 1966, 2-6
TOPIC TAGS: aluminum alloy, magnesium containing alloy, alloy welding,
TIG welding, MIG welding, alloy weld, weld porosity, porosity x*ormation
ABSTRACT: A series of ex e;p_i.ments has been conducted with TIG and 14IG
welding of AMg6 aluminumqTT16'y sheets and plates 2-10 mm thick in order,
to-determine the effect of some variables of the welding process on weld
porosity. it was fo d t.~ -at In welding sections up to 4-5 mm thick,
most of the hyd i'
rogen,11-fg." niates from the surface of the base metal In
welding heav-i-e-F-se-c-tions, the surface of thV"filler material becomes the
main source of hydrogen. Alkaline picklingktollowed by mechanical
cleaning (with a scraper or wire br'ush) shortly before welding ensure
satisfactory cleanliness of the base-metal surface. The filler (elec-
trode) wire in best cleaned by electrolytic polishing, after which the
Card 1 / 2 UDC: 62i.791.753.93.oig:669.715

-K_P6-o-O8_ 11
ACC NRi
wire can be stored for a long time. Alkaline pickling is satisfactory
only if the wire is used immediately after pickling. Otherwise, the
wire rapidly absorbs moisture. Vacuum annealing after alkaline pickling
brings about only slight improvement. It appears that hydrogen nbaorbeA
(as moisture) on the surface of electropolished wire first dissolves in;
molten metal and evolves in the form of small bubbles during cooling.
In the case of wire pickled in alkali, molecular hydrogen does not
,dissolve, but forms bubbles immediately. Decreasing the specific heat
Ankl~~ (by,increasing welding a.pqed) r-educes the total volume of pores
the, evolution' of dissolved,hydrogen and the coagulation of
:,iinill -.'bubbles- into big ones. In multilayer voids however ~,the-
Whi
Miies, co.agul~+.~ -durijig~ h of the next layera-'P,
4K
the 'te -
0 00 S+C EL
v6UAd-caui' ar_~)and~_mir r t;. h a sz,~,.
_f~iziti6n Orig,*. ko.
bk"ODE'. HAD
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- BOLDYRLV, A.N.
Psychotherapy in epilepsy. Vop. psikh. no.4:170-177 160.
(EPILL.-Psy) (PSYGHOTMWY) OURA 15:2)

__ IFVSHENKO, V.F., inzh-,~_~~DY , A.N., inzh.
Assembly and installation of the hydraulic machinery units. Energ,
stroi. n0.23:78-85 961. (IIJRA 15:1)
1. Zamestitell glavno o inzhenera stroitellstva hremenchugskoy
gidroelektrostantsii Mr Levchenko). 2. Nachal'nik uchastka
tresta "Spetc;gidroenergomontazh" (for Boldyrev).
(Kremenchug Hydroelectric Power Station--Hydraulic machinery)

0 0
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09 a!: alumin= oxIde. of soda and of
00 JI!! phelite. A. S. Pold)-ruv. T3r-
00 a i Kkim.
12, Ith-IO(IM).-The nephelite cnnCCntra;e -i; t,

e
010 with fin ly gronud limestone, and then roastcd. Thr

00
mass ul is ground and exid. with a but w1n. of
%ined
~ #4 N
lumiluxt
nd C
l
i
th
N
Th
W
r
e iw
n. con
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ip fft~l (r.113 qi; all~r it yi,ld- A1.0. hv-
=*9
I'liefilletrd
' roe
I fie "Ll
hydiate of AIM is hea". yirlding Al,()..
soln. is causticizO to NaOll. When litnemone is uddv.1 coo
to the nephelite residue (from the production of AI,0,
roe
and soda) a basic raw mattrial for rise production of
'
portland cement is obtained. Nrldiclite cenicut is me-
chanically superlot to limextune-slag cement and lk)zzuo.
larlie cement. W~ It. Ilviin

A S a - i L Aof tAL LVP.GKAL LITERAUAl CLASSIVICA11CO 94-, bow
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BOLDYREV, A.s.
Scientific-research work in the sqrvicq of indugtrv. Leg.prom- 7 no.11:26
N 147. (MIHA 6:11)
(Research. Indastrial)

BOLDYR,h'V, A.S.; GASHIMOV, M.A.
Introduce cementless structural elements into large-panel con-
struction. Stroi. mat. 7 no.10:18-23 0 '61. (YURA 14:10)
1. Zamestitel' predsedatelya Gosstroya RSFSR (for Boldyrev).
2. Glavnyy spetsialist Cosstroya RSFSR (for Gashimov).'
(Ligbtweight concrete)

BUDITIKOV, P.P.; AIZKFERCV, M.S.; BAKUNOV, G.M.,_gQLD-)MEV,-A-S.;
BOBIKO) K.D.; V01ZHEISKIY, A.V.; GROXHOTOV, N.V.; ZHUKOV, A.V.;
ZAW) L.B.; KITAYEVI U.N.; KOSHKIN, V.G.; KRUPIN, A.A.;
14URCUSKIY, P.G.; POPOV, A.N.; SUKHOTSKIY, S.F.; USPENSKIY, V.V.;
IGLINT, I.A.; SHVAGIREV, M.P.; YUSIMVICH, M.O.
Conference on increasing the durability of corrugated roofing
sheets, Stroi.mat. 8 no.l:p.3 of cover Ja 162. (MIRA 150)
(Roofing)

P
OIT)yp,f-,,V,
Pa`rz task for is Le..: ey
.j)Snsfon Of' P7Au^t-3n, lrlc'r-3e;-tng
,y of mat
,he vani-:,t terialn, improvIng ani atrergthenirg
the qc=cn~-. 31roi. mat. ill
w I no.2~;!-,-) F 165. 18,11)
1. Pervyy predsedat.elyiq 'Jasudarstverinapo korz.teta
po promyehlerpost-11. stroitellnykh -Iw~teriulov,

BOIDYREV, B.
Foreign exchange reform in Afghanistan; a note. Den. i
kred. 21 no.11:84-87 N 163. (MIRA 17:2)

BOLDYW, B.,inzh. (Novosibirsk)
Measures for Improving the operation of automatic coupling
mechanisms. Zhol.dor,transp, )6 no,6:80-81 Je 155. -
I (MLU 12:4)
(car couplings)

BOIDYREV.., B.; SKACHKO, A.
"Mbneyp credit and finances Of the Rmpean people's democracies"
bY V.P.Komissarov, A.N*l'bpov. Reviewed by B. ')o:Ldyrev) A~Skachko.
Den.i kred. 19 no'e.10:86-90 0 161. (MIRA 14:10)
(.cope, Eastern-Finance) (Komiss~+ov, V.PO)
(Popov,~ A.N.)

BOLDYRFVI B.B.
Radioisotope device used in pairting In an electrostatic field.
.6
Mashinostroitell no" g39 Je 165. (WRA 180)

CA
in Sipd at v*bw arity of salimilamides
Ckwnsctlan boft"n
k MW b"Wrisiff* actitity of "Haftilamide Com-j
B.-AU--Wddyrev~&nd I ' Ya. Pagovskil (Und.
Ing. im.S. M. Kirovit). Zksdr.O&s4ckfKkim-
Gen. C .) 20. QW-43(IM); cf. C.A. 41, 3WW.-
The salfasilamitle activity is deto. not only by the specific-
Pdarity of the caimpd.. represented largely by the p-
RuissoW remant structures, but allo by the mol. dimen-
swas and sham In comparison with the vitamin with
hich antagonlarn exists. Napbtbakac analop of com-
mm saaallaraides were preg.; these were inactive in I
vim or in riko. Onts substan ting the contention above.
Their tbamotlynamic cm3ts. weft deid- including:
Istats of formation from gaseous ele-
It"Z71= -c# p4ink3 (from comparative data on -
aw 809AZAIJUDIdes, their deaminated analvgs, and naph-
thaknewlionamide). '11w summary of data follow%.
R' -
Jf, R' - Ac, m. 247-81; R' - H. R' - 11, tu. 212-13%
beat of combwtion 1300.6 kcal./mole, beat of formation
77.8 kcal./mak. energy of formation 2139.3 kcal./molt.
p4ink eneW 2.1 kcal./molt " R' - 2-pyridyl, R' - A c,
in. W." .;it, rid)4. R' - 11, m. 231-3'. IW2.9.
50.3.2975.8,13-8;21' - :-thiaxal, R' - Ar,m.2'o3-4';-
R' z4biesolA R' H. W. -2 - - - - --
R' - Ac. m. 252-3';
pkWkyi, R' -_ ff. m. 211 *,
2492.4. 16.9-.'4045.9.- 2'816. Compdo. of type I-RX11- i
C it. m. 149-50% 12M.8. 73.4. 1998.5.
Uyl,in. 214-15% J? -
m. 229-M'. 24PA.M. 131.2.
31178.8, - CcqaP-i- of -ergY of P-links lot xMI'Mil-
ainkles wW their napbtbyl atudop xiv", resp., the FoDow.
Z101 values in kcal./mole: sulfanilamide 3.2, napbtbyl
analog 2.8, sullapyridine 15.2, Its napbtbyl analoir 13.8.
G. hl. Kosol&DoIT

CA
The VESI so
=b=
sm " B. 0. RaWyrrv sud 1. Va.
postorsu. J. G!:rc"
(Husl. tmnsktkm).,qcl C-4-44, OUlf. R. M. S

77
r
RA b.
(153brbri KASM.' Mail. I-VanAr ~5.5zdi. 1'~
614-2509M)-it was,Nhown by txpt. that- thtm is no
vxrclati-n brttitol the chavactcris?k ph)sloWcal actlAty;
of the iulfoiumHt;~ nrld Olt -IDnadditWily of their ruersit, - -&nriMy wm obta
Of fmnatiRll W. l'tj%l&lrrra rinil Xokoshl~o, CA. 41, (R And R' zbown): Ac, 2-pyriiiyf,
'W"Pe). Cowlt-tr-minji of the appriipriale sulfalry) r-hlo- D1. 2232-3". H. 2-pyrid7l (111), tn. 213-14'; Ac, 24U=4~4,
rides wilb napblh~njatnldu 'ur sullanilarnide in ~yfidine, M. Z53-4% I!, 24hia:a-4 m 201-3'. Abo %yrre pr,-pd.
10101yed b- ficacetvbtion it) 2:1 aq.-MO)MIC1. gave: Kn, 220-l', and I-Cg~ff,-
(1), tn. 216'; P,4cATJIC~Hj- SCWh -R' 0? imd R A&VO: Ac. It. m. 240'; H, H (VD,
rn,=%
Tile &O-Ition a exp1l. ra-at of formation 'from F-Vil- beats of combustion (cal./gj: V. b534; 1. 5,3779;
theeJard. valuefor thisgroup was 7.4k-cal,/mOeforthL jst. IV, 5519; 11, 5375;
ilid 3.5 kcnl./TnOe for th!! 2nd sullonatnijr,; tlane -hwe SOoNfl:, ZC-P-; W2; 111, 6120;
pbr-3al.;lctive. 'Similarly all 2-CJ1,SOl1Vqs. GD-11; and V7, 5719. 0. M. Kosolapoff-
lhaknz v-crc I)b-plol. inactive although corlsiderable--e--
wd -h=t Gf- 11--natiou ii fonjvd -izr -this- -2i. I tD-68-
kcal./inoM. Antidatinn o1, j -nctLnmidrAiapbthj1-7=A-
7- fonvi chlorkic followed by hydroly.;'is with HQ (d. 1,CR)
.5-stiffenanjide. rn.2&S-q*
r1. Ber. 23. 1118(18W.)j, and the I-amino c?ji;l vZ"

TZV, D. G.
Btatey
On Some Sulfamides of the Naphthalene Series, pege 616. Sbornik/po obshchey
khimii (Collection of Papers on General Chemistry)t Vol 1, 140scow-Leningradl
1953, pages 762-766.
Laboratory of Organic Chemistry, Ural Polytechnic Inst imeni S. M. Kirov

ynthes s anti some properties of lumlq. of
allicin B. G.. Bolclyre,--and A. T. Zak-barchuLYS(ZZ
tech, I -----tT ff.-~', y Akad. Nalthi S.S.S.R. 94,
877-!)(lP54).-Condenq!i t ion of C11,:CHCHI9Q-SK iritli
RBr ill "1q. Nle.,CO at room temp. gave a 70~,'c yield xvith -
11,11 bromide only; other alkyl bromides Cave only 5-65o
yields asid the produeu were IdentifiPti only by 8 analysis.
The prodiwLs Nvcm vvllow Ii quids %vith a Mrong garlic or
onioa odor and enulif tiot be di4d. evenal. 1-2 ram, Treat-
tucist of 'Me1S(_),Cl with.KS11 gave IPSO~SK, m. M1-2%
which is-a- Own treateff ivith R13r vielding [lie following
e.,term;: Iri-SOiSEI, 1.2531, W.' L.-jO319,
l.S%; Pr imab:~, 1),-! I()(;-7'. d." 1.1945. n" 1.4994,
v
i.w-Pr I$- MS67, nzio, I .;A38.
!W Rn bi- lW-17", di'~' 1.1510, ii~7
I 3T.51 . '02!1111"' ill-. 101-,1", 1.1492. ill"
I'lit'r pro'hirt, 1vt-rc, eolorlu"36 %'fith 11
Z~Iflic or ol;;"ll and mt" Slil;!t, a't-%WQ ill swr'lgv at Tolmn
G. M. Ko-'4il.lj"3ff

A Inn. - -3 r-a I-L S;S.R~
'c0
a ;D-
'
~Ydr y1mrin (1) fro. iliLx ;4rate pocis ~J

td n 0 hr5. vs-i Lh I : 3 rn-,L- r rai t iD, re-qp, of the
6
-1
rca-ztarti- YiPliscl 4 M ottvimA imdrr thtse coridi-
'
--Ied jube yields 2,r.&Irichlc~ro-
I ~.ith PK41ri st
pur;De (11), the bLrst r,-,Mlt3 (877% vield) bring att'-jn[d with
lco-fo'd Ivular propm-tion 61 PM., at 165'; the excer'3
'POCII; must be complet0y distd. Were treatment with 11t0
--drolysis of, thk-- prMurt.' Pure 11
to tlrfTt t P~ -00 b,
IND-l'. H With 1040A cle-CS9 of 25% N-H.Oil ii -"-'llcd
tlibv 6. hm lit 100* 'gave Ozl% arat
'
b
d
t i
i
g
ft
ith C
d
905
n
uc
s v
m
w
aii
b pure pro
a
er trrattntut
my.-to-l'-wrl

y

BOLDTTM, . B. G.
The priority of Russian scientists In syntheses with
metalorganic compounds of the Rql type. Naucb. zap. LPI
no.29:3-6 155. (MLRA 9:10)
(Organometallic compounds--History)

BOLITfREV, B.G.; IVAKINA, M.A.
Some analogues of peaudoallicin (V10 02 SPO- Uuch- 'aP-
LPI no.29:109-120 155. (MLRA 9:10)
(Allicin) (Antibiotics)

BOLDUR. B.G.; LITKOMS, A.I.
Syntheses and properties of certain alkyl ethers of ethane thiosul-
phonic acid. Dokl.AN &5M 107 n0-5:697-699 Ap '56. (HLRA 9:8)
1. L'yovskiy politakhnichoskly institut. Predstavleno akademikom
I.M. Nazaro"u.
(Sulfonic acids)

i4d ~Tr,
~4 i: b~
1-1~- 2.1 2; 62~K, 302-3-,'
193. 1.4qi'-
'IM 'IAMi - 61-3%,,Bx, b)-:i )1Z-13% LOSSS, .1,4W*'
For is
B b~~- 104-V, 1.0975,A 4V-0.
-
O-
7VO'b IDS
-
,
" lee.
5
,
1.5039; ~4.6%,Ba, bi-2 123-44, 1.0599i 1.48211;
ARA. , Mip estm,
1.0069, 1
1~b 4'
-fiere active 0.
B.-, and spedti of Pen-'r0lium, Aspefliual,

-izapus. lr~cor-ip dilu~. Of g=cyally~
), and
B
e
I I I
f th
b0
Mo
t
ti
0
2
0W
1
OM
5
(i

-
ve
.
o
e a
v
s
ac
t
.
n
DI
o 1;
,
mge .1 co.m.). Irm h~FxSovscmlex and iso-WSOB~
ms.
CHIcum.

20-5-27/60
~T'a H a It DOLDYREV B.G., GINZBURG J. S. , DRABIUNA) R. 0.
TITLE On the Antituberculoua Activity of Thiosulfonic Acid Ethers.
(0 protivotube'rkaleznoy aktivnosti efirov tiosallfoktslot-Russian)
M10DICAL Doklady Akademii Eauk SSSR,1957,Vol 11-,j,Nr 5,PP 1o14-1o16(U.S,S.R.)
ABSTIUCT This activity of I thiosalfonic acid ethers has hitherto not been
investigated at all.Only in one instance did the bacteriostatic
action of II ethanethiosulfonic acid on 124yoobacterium tuberculosis
became known. In vievi of the fact that the stractare of the IV-com-
Dounds is exDressed by their anti-tuberculous properties,the authors
hoped to detect substances with such properties among the ethers of
I thiosalfonic acids.Alkyl ethers of alkane thiosulfonic acida.Clo-
sed to the allicin-analogues according to their structure are the
alkyl-ethers of V alkane th-Josulfonic acids,vihich vere already ear-
lier synthetized by an author.These substances have a broad anti-
bacterial action spectrum and exhibit in vitro a bacteriostatic in-
fluence on g-ram-positive,gram-ne-ative and acid-resistent bacteria,
on various fungi,protozoa,etc.Tests in vitro. All of the ethers te-
sted showed a tubercolostatio affect. All ethers of metlh.:,ne thio-
oulfonic acid and propane thiosalfonic acid-2 fully retain their ac-
tivity even in the presence of oeruia,in contrast to the alkyleth-
ers V of the other alkane thiosulfonic acids.Tests in vivo.The pre-
par'tions found to be most active in vitro were tested on white miae
a
for their toxicity and their deadly action determined in various
Pard-1/3 _ozies.The least toxic substances among th~.-ja were tested for clari~-

20-5-27/60
On the Antituberculous Activity of Thiosalfonic Acid
Ethers.
fication of their therapeutical effect on experimental tuberculosis.
All ethers examined,also those with a maximum activity in vitro,,we-
re ineffective on that occasion.In some irstances this may be ex-
plai'ned by their ability to inactivate themselvea abruptly in ani-
mal organisms,in other instances it may be explained by their ele-
vated toxicity which prohibits its application in large doses.
Alkyl ethers of benzene thiosalfonic acid and their derivatives.The
VI etherre have the same effect ori the same types of bacteria as tho-
-.;mentioned above.Their activity,however,is weaker than that of
-the V-com.-jounds.Tests in vitro.The introduction of substituents in
a p-position.also little changes the activity; chlorine,and the me-
thoxy,--roup slightly raise it.The nitro group has no noticeable ef-
.fect,the acetylamine group slightly reduces it;the deazylation of
the alkyl ethers of acetylthionulfonic aeLd increases the activity
of these compounds.The mutual position of the substituents in the
benzene nucleus apparently in insignificant for the t-uberole-kil-
ling properties.Here.too.an inactivation by serum takes place.How-
ever,no established connection between structure and inactivation
could be found.Tests in vivo.Three VI alkyl ethers with ail activi-
ty of ca.1 ffig,which cannot be inactivated by seriim',were tested.No
Therapeutical effect was noticed.Thus the tested substances have a
gard 2/3 tubercle -static activity in vivo,but are ineffective in the ouring

ZU-5-27,rW
On tlic Anti tuberculous Activity of Thiosulfonic Acid
Ethers .
of Vabercf4losis or, living animals.
(4 Slavic references)
ASSOCIATION L I v ov -~olytechnical Institute and Ukrainian Scientif ic Research
Inatizate for Tuberculosis.
P4E:3Wrl:D BY TIAZLROV I.N.,A','eiaber of the Academy.
SUB11TTIZ 25.2-1957
AVAILABLE Libraty of Congeess.
Card 3/3

'r
:7
AUTHORS: ~Ityukova, K. I., and Boldyrev, B. G. 20-3-40/52
TITLE: Ethers of Thiosulfoacids as New Means of Combating Bacterial
Plant Diseases (Efiry tiosullfokislot - novyye sredstva
dlya bor'by a bakteriallaymi boleznyami rasteniy).
PERIODICAL: Doklady AN SSSR9 1957, Vol- 117, Nr 3, PP- 500-503 (USSR)
ABSTRACT: The second author undertook an extensive synthetical work
for the research of new bactericidal action based on the
efficiency of two others: "Pseudoallizin" and ethane-
thiosulphonic acid-ethyl ether against bacteria (re-
ference 4). According to their structure the alkyl ethers
(VII, VIII) of the alkan- and aren-thiosulphonic acids are
closest to the allizin. The second author has synthesized
80 such alkyl ethers (reference 4). Their antibacterial
properties proved to be versatile: They have a bacterio-
static effect (as required fungistatic and protistozid) upon
gram-positive and -negative as well as acid proof bacteria,
various fungi, protozoe and others. Their antibacterial
properties vary within relatively narrow limits according
to their structure. Most active are the isopropyl- and
isobutyl ethers of the cited acids. Present work was carried
Card 1/4 out in order to find out about the effect of the ethers

Ethers of Thiosulfoacids as New Means of Combating 20-3-40/~2
Bacterial Plant Diseases
VII and VIII upon various kinds of bacteria. 40 different
strains of 22 phytopathogene bacteria (Tab. 1) were examined.
It was established that all ethers VII and VIII act
bacteriostatio upon all strains, and only rarely show no
bacteria-killIng effect. Alkyl ethers VII of the cited acids
are most effective against the bactericidal action of plant
diseases of the species Xanthomonas. A certain tendency of an
increase of the resistance against these substances showed
the phytobacteria of the species Corynebacteriuml and more
resistant are the kinds of the species Pseudomonas and
Erwinia (Fig. 1). Some ethers, nevertheless, were effective
against most resistant bacteria also in dilutions of
1 : 200 000 - 1 : 500 000. Alkyl ethers (VIII) of the
benzene-thiosulphonio acid are as much active against
Xanthomonae, as the ethers VII, but lacks behind as regards
the effect upon Corynebacterium and even more so as regards
Pseudomonas and Erwinia. Some alkyl ethers VIII of the same
thiosulphonic acid were highly active against Xanthomonas
and were effective even in a dilution of 1 : 1000 000, so
Card 2/4 that they exceeaed all other others. The introduction of

Ethers of Thiosulfoacids as New Means of Combating 20-3-0/52
Bacterial Plant Diseases
X-substituents into the p-position to the thio-ether-group
of the benzene-thiosulphonic acid lessens the activity; to
a small extent this holds for the groups: - OCH -C1 and
NH 2' to a larger extemt for the groups: -N 02 an~ NHCOOCH Y
The discussed preparations are harmless under certain
conditions and at adequate application for the tissues of
seeds of more-years old leguminous green fodder, of kinds
of vegetables and corn. On the contrary, they improved the
germinating capacity, raised the weight and the size of the
germs, and reduced the number of infected germs. The results
of the experiments on fields with the treatmert of seeds of
various agrilculturally useful plants (cabbage, lucern,
tomatos) are summarized in the tables 3 - 5.
There are 8 figures, 5 tables, and 7 references,
6 of which are Slavic.
ASSOCIATION: Institute for Microbiology of the AN of the Ukrainian SSR.
L'vov Polytechnical Ins'.itute (Institut mikrobiologii
Card 3/4 Akademii nauk USSR,'Ilvovskiy politekhnicheskiy institut).

20-3-0/52
Ethers of Thiosulfoacids Al'ew Means of Combating
Bacterial Plant Diseases
PRESENTED: January 2, 1957p by S. I. Vollfkovich, Academician
SUBMITTED: October 27, 1956
AVAILABLE; Library of Congress
Card 4/4

AUTHORS: Boldyrev, B. G., Kofman, Yu. 1. 79-28 -3-44/061
TITLE: rnv.~7m =
stigation Within the Field of Thiosulfo Acid (Issledovan-
iye v oblasti tiosullfokislot). III. Alkyl Esters of Phenyl-
methanethiosulfo Acid and Its Antiseptic Properties (III.
Alkilefiry fenilmetantiosullfokisloty i ikh protivobakteriall-
nyye svoystva)
PERIODICAL: Zhurnal Obshchey Khimii, 1958, Vol. 28, Nr 3, PP. 768-769
(USSR)
ABSTRACT: In earlier works the authors observed in the investigation of
alkyl esters (I) of alkanethiosulfc, acids that the antiseptic
activity of these compounds does not depend on the size and
the structure of the radical at the oxidized sulfur, and that
the activity practically remains the same for the esters of
thiosulfo acids when they are of normal structure and when the
11"Iber of carbon atoms does not exceed four. For this reason
the authors decided to synthesize and investigate more closely
the alkyl esters (II) of phenylmethanethiosulfo acid in order
Card 1/3 to check with this example how the change of the char-

Investigation Within the Field of Thiosulfo Acid. 111, 79-28 - 3-44/61
Alkyl Estero of Phenylmethanothioaulfo Acid and Ito Antioeptic Properties
acter of the radical of thiosulfo acids acts on the anti-
septic activity of the esters. The synthesis of the alkyl-
phenylmethanethiosulfonates vas carried out according to the
earlier described method (reference 1); the obtained esters
are listed in the table. They are colorless, crystalline
compounds with weak but specific smell, mid they are easily
soluble in alcohol, ether, acetone and other organic solvents
but difficulty soluble in water. The investigation of the
antiseptic properties of these esters (II) which was carried
out by the Institute for Eicrobiology, of the AS USSR showed
that the activity of these compounds compared -with the Gram
positive, Gram negative and acid-proof bacteriais smaller
than with the alkyl esters of the alkanethiosulfo acids with
a number of carbon atoms from 1-4; at the same time the
activity of the esters increases considerably compared with
the various fungi. Thus the present work proved that the anti-
septic properties of thiosulfo acid not only depend on the
character of the radicals bound with sulfide sulfur but also
on the structure of the initial products, the thiosulfo acids.
There are 1 table and 4 references, 2 of which are Soviet.
Card 2/3

Investigation Within the Field of Thiosulfo Acid. 111. 79-28 ~-44/61
Alkyl Esters of Phenylmethanethiosulfo Acid and its Antiseptic Properties
ASSOCIATION: Llvovskiy politechnicheskiy institut (Polytechnical lnstitute~
Llvov)
SUBMITTED: FebruarY 4, 1957
Card 3/3

AUTHORS: Bol re ,,, Trofimova, T. A. SOV/79-28-7-47/64
,y"T.-Y .
TITLE: Investigations in the Field of Thiosulfo Acids (Issledovaniye
v oblasti tiosullfokislot) IV. On the Reaction Mechanism of the
Formation of Thiosulfonates(IV. 0 mekhanizme reaktsii obrazo-
vaniya tiosullfonatov)
PERIODICAL: Zhurnal.obahchey khimii, 1958, Vol. 28, Hr 7,
PP- 1940 - 1944 (USSR)
ABSTRACT: Alkane- and arene-thiosulfoacids can be obtained in the form
of salts RSO 2SMe (I) by the action of the halogen anhydrides
of sulfo acids on aqueous solutions of potassium sulfide(Refs
1-4). In this reaction process elementary sulfur seprarates.
It is assumed that (Refs 2,3) the thiosulfonates (Formula I)
are formed according to the Oeneral schemes (1) and (2):
RS02Cl+K2S RS02K+KC1+S(l ), RS02K+S RS02SK (2). It was
therefore of interest to the authors to find Dut whether the
earlier mentioned conceptions concerning t7he formation of thio-
sulfonates were correct, this the more since just that way,ikej~y
Card 1/3 the reaction of sulfochloride with potassium bisulfide, 20

Investigations in the Field of Thiosulfo Acids. IV. SOV/79-~8-7-47/64
On the Reaction Mechanism of the Formation of Thiosulfonates
salts of various thiosulfo acids had been synthebized already
earlier (Refs 5-9), In order to prove the possibility of a
binding of thiosulfates according to the reaction (2) the
potassium salt of the acetyl. thiosulfanilic acid was produced(II).
Following the mentioned reaction scheme the authors realized,
on the basis of this compound, the synthesis of the thiosulfo
salts of halogen anhydrides of the sulfo acids and alkali bi-
sulfides through the intermediata stage of formation of sulfinic
acids. Thus it-' was shown that the synthesis of thiosulfonates
from the salts of oulfinic acids and elementary sulfur is
possible. There are 12 references, 9 of which are Soviet.
ASSOCIATION: Llvovskiy politekhnicheskiy institut (Llvov Polytechnical
Institute)
SUBMITTED: June 5, 1957
Card 2/3

Investif,ations in the Field of Thiosulfo Acids. IV. SOV/79-28-7-47/64
On the Reaction Mechaniam of the Fornation of Thiosulfonates
1. Thiosulfonates--Synthesis 2. Halogen anhydrides--Cheniical reactions
3. Potassium sulfide--Chemical reactions
Card 3/3

AUTHORS:
TME:
SOV/20-121-5-43/50
A01 -IL, G. Drobot1ko, V. G., Ayzenman, B. Ye.,
Zelepukha, S. I.
On the Antimicrobic Activity of Alkyl Esters of Thiosulfuric
Acids (0 protivomikrobnoy aktivnosti alkilefirov tio-
sullfokislot)
PERIODICAL: Doklady Akademii nauk SSSR, 1958, Vol. 121, Nr 5, PP. 924-927
(USSR)
ABSTRACT: The above mentioned properties of the esters (I) of the thio-
sulfuric acids were only recently properly investigated for the
first time. According to the authors the synthesis of these
esters and thestudy of their bactericidal properties is prom-
ising (Refs 1, 2). This is supposed to be the way to develop
new active medicaments. First of all, alkyl esters (V) of
alkane-thiosulfuric acids which correspond best to the natural
antibioticum "Allizyl" were synthesized by the first author
(Ref 3). The antimicrobic activity was studied on Staphylo-
coccus aureus, B. coli, 14ycobacterium Bq, and on various spe-
cies of fungi, also on water infusoria, _' on the dysentery bac-
Card 1/3 terium, on blight spores, and on others. The activity of the

SOV/20-121-5-43f5O
On the Antimicrobic Activity of Alkyl Esters of Thiosulfuric Acids
alkyl ester (V), treated in this paper, of the alkane-thio-
sulfuric acids changes according to their structure within a
rather limited range. This applies also for the fungistatic
activity: The esters of phenyl-methane-thiosulfuric acid and
of the 2-methyl-propane-thiosulfaric acid-1 are the most
active of all compounds (V) examined. The accumulation of
thio-ester groups does not lead to a positive result. The at-
tachment of a chlorine atom to the p-position with respect to
the thio-ester group scarcely modifies the activity, the at-
tachment of the CH CONH-group, however, decreases it. The
esters of the thiolulfanilic acid exceed most of the all;yl
esters (V) in their antibacterial and fungicidal properties.
The obtained results prove, that the structure and the size of
the molecules of the 'esters in question are not crucial
criteria for the rate of antibacterial activity. Therefore,
investigations in this direction ar~ to be carried on. There
are 1 table and 4 references, 3 of which are Soviet.
ASSOCIATION; Llvovskiy politekhnicheskiy institut (Polytechnical Institute
L'vov) Institut mikrobiologii im. D. K. Zabolotnogo Akademii
Card 2/3 nauk USSR (Institute of Microbiology imeni D. K. Zabolotniy,

SOV/20-121-5-43/50
On the Antimicrobic Activity of Alkyl Eaters of Thiosalfuric Acids
Academy of Sciences, Ukrainian SSR)
PULSENTED: March 20, 1958, by V. N. Shaposhnikov, Member, Acaderay of
Sciences, USSR
SUBMITTED: March 20, 1958
Card 3/3

... . .. -- -, - c-'--
BOILDYREV, B.G.; TROPIMOVA, T.A.
Thlosulfonic acids. Part 5t Syntheses and antimicrobial properties
of some alkyl eaters of benzenethiolulfonic acid ard its derivatives.
Zhur. ob. khim. 30 no.12:3993-3998 D 160. (MIRA 132-12)
I. LIvovekiy politekhnichaskiy institut.
(Benz enethi osulf onic acid)
.0

S/020/60/132/02/2c3/06'11
B0111B002
AUTHORS: Boldyrev, B. G., Gar, K. A., Yevtoyeva, N. V.
TITLE: Esters of Thiosulfonic Acids as New Fungicides~
PERIODICAL: Doklady Akademii nauk SISSR, 1960, Vol. 132, No. 2, pp. 346-348
TEXT: Esters (I) of thiosulfonic acids are effective against microorganisms
within a wide range. They also stimulate the development of plants thus increas-
ing harvest. The authors investigated the fungicidal properties of methyl eaters
of alkanethiosulfonic acids (III), and the trichloromethyl esters (IV) of these
acids. The authors do not agree with the American investigators (Ref. 3) as
regards the assumption that the fungicidal effects of trichloromethyl esters of
d i f f e r e n t thiosulfonic acids are the same, regardless of the nature
of the radical (Formula IV). This was disproved by the authors (see below). They
also tested some aryl esters (V) and (VI) of alkane- and arene-thiosulfonic
acids. The fungicidal action of all these esters was tested in the toksikologi-
cheskaya laboratoriya (Toxicological Laboratory) of the Institute imeni Ya. V.
Samoylov (see Association) in the following species of fungi: Diplodia zeae,
Alternaria radicina, Verticilium dahliae, FuBarium vasinfectum and Fusarium
Card 1/3

Esters of Thiosulfonic Acids as New Fungicides S/020/60/132/02/28/067
B011/BO02
oxysporum. Certain concentrations of these preparations dissolved in acetone,
were introduced into agar nutritive media, into which the fungi then were sown,,
The action of the esters was determined after 5 days. Similar experiments with
equal concentrations of Figon, Kaptan, and Tsineb were conducted for
comparison. Table I shows that trichloromethyl esters of alkanethiosulfonic
acids are the most effective among all substances examined W. During experi-
ments in vitro they had a much better effect than similar esters of arenethio-
sulfonic acids. This action, however, is not due to the trichloromethyl group;
the substitution of chlorine atoms by hydrogen atoms influences the activity of
the compounds under consideration. The special effect of the nature of the acid
radical R becomes evident during transition into the aryl esters of thiosulfonic
aGidS ~V) and (VI). While the aryl esters of methane- and ethanethiosulfonic
acids Table 1, No. 10-13) are still strongly fungicidal and even surpass the
trichloromethyl esters of arenethiosulfonic acids (No. 7-9) in their action,
aryl esters (VI) are considerably less active than other esters (I). Some of
them, however, are not inferior to fungicides as active as Kaptan. The esters
discussed here, particularly those of alkanethiosulfonic acids are thus highly
active fungicides and are worth further investigation. The action of the
fungicides was investigated in the Institut mikrobiologii AN USSR (Institute of
Card 2/3

Esters of Thiosulfonio Aoids as Pew Fungicides S/020/60/132/02/28/067
B0111B002
Microbiology of the Academy of Sciences, UkrSSR). There are I table and 2 Soviet
references.
ASSOCIATIONt Llvovskiy politekhnicheskiy institut (L'vov Polytechnical Institute).
Nauchnyy institut po udobreniyam i insektofungitsidam im. Y-a. V~
Samoylova (Scientific Institute of Fertilizers and Insecto-funzi-
oides imeni Ta. V. Samoylov)
PRESENTED: January 13, 1960, by S. I. Vollfkovich, Academician
SUBMITTED: January 3, 1960
Card 3/3

BOLDMIEV, B.G.; GORELOVA, S.A.; DVORKO, A.T.
Thiosulfonic acids. Part 6: Syntheses and antimicrobic properties
of irichloromethyl and methyl esters of some thisulfonic acids.
Zhur.'ob.khim. 31 no.7:2402-2406 Jl 161. (MIRA 14-.'7)
1. Livovskiy politekhnicheskiy inAitut.
(Sulfonic acids)

BOLDYREV, B.G.; KIIOVALKO, L.M.
Thiosulfonic acidis.- Part.7.- Aryl eat-irs of benzenothiosulfonic acid
and its deftyativos. Zhure ob. khim. 31 no. 11:3729-3734 N 161.
(MIRA 14: U)
1. Llvovskiy politakhnichealtiy institut.
(Benzeriesulfonic acid)

BOLDYREV, B.G.; YUSMVICE, L.N.
Thiosulfonic acids. Part 8: Alkyl asters of thiasulfonic
acids, derivatives of naphthalene " phenanthrene. Zhur.ob.kbiyn.
3) no.3:969-973 W 163. (MIRA 16:3)
1. Llvovskiy politekhnicheakiy institut.
(Naphthalenesulfonic acid) (Phenanthrenesulfonic acid)

BOLDYREV,.BAG.~. KOLMAKOVA, L.Ye.; BILOZOR, T.K.
Thiosulfonic acids. Part 9; Diesters of thiosulfonic acids.
Zhur'.ob.khim. 33 no.6:198OL-1983 Je '63. (MIRA 16:7)
1. Llvovskiy politekhnicheskiy institut.
(Sulfonic acids)

BOLDYREEV, B.G.; KOVBUZ, 11-II.A.; TRUDIOVA, T.A.
Thiosulfonic acids. Part .10: Reduction of t-*hiosuI-Ifc~rA',-, ar;Id
esters on a mercury dropping electrode. Zhur. ob. "'him. 35
no.1:22-27 Ja 165. (MITFL4 18:2)
1. Ltvovskiy politelffinicheskiy institut.

... BO.LDMFV, B.G.; KOLESNTIKOVA, S.A.
Tulfonic aczd esters with ami-t7z- -n1..'. - ,,.
Reactions of tj,,io-
kUm. 35 no.1,198-199 v7a 165. Ovllil~k- ~
1. I,Ivovskiy politeklinichaskly institut.

SOSEDOV, I.S.; WLDYREV, B.M.
Yap of the annual average runoff of eastern Kazakhstan rivers.
Trudy Otd. peog. All Hazakb. SSR no.8:162-1 3 161- (MIRA 14:8)
(Kazakhstan--Runoff~

- T - --- - - -
BOLDYIWV, B. _glavnyy matodist pavillona-, DVORNICHENKO, I., red.
I --I-
[*Medical equipment industry* pavilion] Pavillon "Meditainakaia
promyshlennoBtl"; putevoditel'. Moskva, Medgiz, 1957. 31 P.
(MI" 11:3)
1. Moacow. Yeesoyuzuaya promyshlennaya vyBtevka, 1956-
(MOSCOW--MEDICAL SUPPLIRS--BXHIBITIONS)

- - --- - , -. - . r
B OIDYREV, B .Y .
.i-r,ie-f*-n`e-lw-s'. Ked.prom. 11 no.8:63-65 Ag '57. (MIRA 10:11)
(MEDICAL SUPPLIES)

BOLD-M.N. B.V.
New medical Apparatus at an exhibition at the All-Union Resenreth
Inatitute of Medical Instruments And ADPRrstun. Hed.prom. 12
no.4:63-64 Ap 159. (MIRA 11:5)
(MBDICAL INSTRUMMS AND APPARATUS)

YFMMIN, V.V.; NESTWWWO, A.T.; KOVMUROVA, L.A.; RAZUMOVSKAYA' Ye.I.;
OSIpOVA, ye.y.; VASILrIEVA. G.s.; PRXA=1Y, M.D.. otv.red.;
ZVCROHO, B.P., zamestitell otv.red.;'BQLDYRE7, B.V., red.; VOLODIN,
Ye.A., red.; DANILICHERKO', Te.peq red.; MI5HIH,
L.N., red.; FREYDIN., G.S., red.; TWMN, TueA.9 red*
(Technological instruction material; aluminum and aluminum alloys
for medical articles] Rukovodiashchie tekhnicheskie materisly;
aliuminii i aliuminievye splavy'dlia meditsinakikh izdelii. Moskva,
H-vo zdravookhrananiia, 1959. 70 P. (MIRA 13:8)
1. Vaesoyuznyy nauchno-iseledovatellskiy institut meditsinskogo
instrumsntariya i oborudovaniya.
(NOICAL INSTRUKWS AND APPARATUS) (ALUMINUM)

Bolj)ynv, B. V.
Spirograph; information. Iab. delo 5 no.1:61 Ja-F 159. (MIRA 12.1)
(SPIRDSCOPE AND SPIROSCOPY)

BOLD'MV, B. V.
Exhibition of new -aroductions at the All-Union Research Institute
for Medical Instruments and Equipment. Med. prom. 13 no-5:63-64 My 159.
(MEDICAL INSTRUMMTS AM) APPARATUS) (MIRA 12:7)

--WLDMV. 3.T.
Now viedical products at
Research InstItut6 for
prom. 14 no.6t63-3 of
(NIDICAL
the exhibit of the All-Union Scientific
Medical Instruments and Apparatus. Nod.
cower is 160. (MA 13:6)
INSTRUKMTS AND APPARATUS)

BOLDME79 B.V.
The national enterprise, "Prema." Med. prom. 11, no.7:59-61 je '60.
(MI-RA 13:8)
1. Vsesoyuznyy nauchno-isaledovatellskiy institut meditsinskikh
instrumentov i oborudovaniya.
(OZECHOSLOVA,KIA-MEDICAL INSTRUME14TS A14D APPARATUS)

BC~l~ ",,V.--
Exhibit of new developmenta of the All Union Scientific Research
Institute of Medical Instruments and Equipment. Nov. med. telch.
no.2-88-91 161. (MIRA 14:12)
(MEDICAL INSTRUMENTS AND APPARATUS)

-ii-OLDMEVY B.V.
Exhibition of new equipment at the All-Union Research
Institute of 14edical Instruments and Equipment. 1(.!1'e1dW.tp1r5om:3.)
15 no.6:60-61 Je 161.
(14EDICAL INSTRbNENTS AM APPARATUS)

SMIRNOV, I.P., kand. tekhri.nauk, otV. red.; MARSHY, M.D.,
kand. tekhn. nauk, zam. otv. red.; jjq~ljlmr, B.V.jp
red.; VOLODIN, Ye.A.p red.; GAYSINSKIY, B.Ye., red.;
DANILICHENKO, Ye.P., red.; KA3ATOV, Yu.F., red.;
KALANTAROV, K.D., red.; MISHIN, L.N., red.; OHSKIY, I.N.,
red.; FEDURKBJ, V.V., red.; TSEPELEV, Yu.A.., red.
[Materials of the scientific session devoted to the 25th
anniv%rsary of the All-Union Scientific Research Insti-
tute for Medical Instruments and Equipment] NAterialy
nauchnoi sessii, posviashchennoi 25-letiiu VNIIMIO. Mo-
skva, 1962. 65 p. (MIRA 17:2)
1. Moscow. Vsesoyuznyy nauchno-issledovatellskiy institut
meditsinskogo instrumentariya i oborudovaniya. 2. Zame-
stitell direktora Vsesoyuznogo nauchno-issledovatellskogo
instituta meditsinskogo instrumentariya i oborudovaniya
(for Pekarskiy). 2. D-4rektor Vsesoyuznogo nauchno-
issledovatellskogo instituta meditsinskogo instrumentariya
i oborudovaniya (for Smirnov).

BOLDYREV. D. [Boldyrau, D.]
You grow young again if you work with children. Bab. t sial
36 no. 7:20 J1 160. (MEU 13-10)
(Mogilev-Physical, education for children)

, -.- Ir,
/ BOIJ)YRAV, D.V.
- , -
Ifore on the determination of drilling "eds. Neft. khoz. 36 no.l:
29-30 Ja 158. (MM 11:2)
(Oil well drilling)

BOLDYREV, D.Vi
Seasonal periods in test drilling, Neft. khoz. 40 no.10-.
6-8 0 162. (MIRA 16:7)
(Oil well drilling)

-1301DYREV, G.
Achievements of the chauffeur and innovator Sitnikov. Avt.transp. 32
no.9:23 S 154. (MLBA 7:11)
1. Glavnyy inzhener Zimovnikovskoy avtoroty "Soyuzzagottrane.6
(Sitnikov, U.N. )

BOLDYREV,G.
Improve the quality of trailers manufactured at the Irbit
Plant. Avt. transp. 33 no.4:37 AP 155. (MIRA 8:7)
(Irbit--Automobileo--Trailers)

BO TUV,, G..
Experience of operations of the Zimovniki automotive unit. Avt. transp,
33 no.5.*13 my 157.' (XLRA 10:6)
1. Glavnyy inzhoner-Z.Imoynikovskoy avtomobillnoy roty Rostovskogo
oblavtotresta.
(Zimovniki--Transportation, Automotive)

AdKSEYW, A.Te.; BAYKO, V.F., kand.tekhn.nauk; BOLDTIM'o G.L., inzh.
NORNLTSKIT, B.L. kand.takhn.nauk, dots. V.- , inzh.
Gomparing the static and dynamic characteristics of two and three-
stage longitudinal field rotary amplifiers. Elektrichestvo no.12:
24-26 D 157. (MIRA 10:12)
1.1eningradakiy elektrotekhnicheakiy inatitut Im. Ullyanova
(Ionina). 2.Ghlen-korrespondent AN SSSR (for Alekseyev).
(Electric generators)

I
ALEKSBYAV, A.To.,prof.: BATKO. V.P..kand.tei--hn.nauk;__PPILDMET, G.,L.,insh.;
NORNEVSKIY. B.L.kand.tekhn.nauk, dote.; ROSIN, Ye.I.,Inzh.;
-CHUPYATOV, I-N--,kand.tekhn.nauk, dots.
Internal feedbacks In multistage amplifiers with various numbers
of terminal pairs. Sbor.LIIZHT no.159:232-235 158.
(MIRA 12:2)
1. Chlen-korrespondent AN SSSH (for Aleksayev)-
(Rotating amplifiers)

s/196/62/000/004/022/023
E194/E155
AUTHOR: Boldyrev, G.L
TITLE, methods of improving amplidyne characteristics
when used in electrical transmission circuits of
diesel locomotives
PERIODICAL: Referativnyy zhurnal, Elektrotekhnika i energetika,
no.4, 1962, 7, abstract 4 L27. (Sb. tr. Leningr.
in-t inzh. zh.-d. transp., no.175, 1961, 42-52).
TEXTs Automatic control systems for diesel-electric
locomotives require further improvement, particularly in the
power circuit where an important part is played by amplidynes
which are used to excite the main generator of the locomotive.
In 1957, the Kharlkovskiy zavod teplovoznogo elektricheskogo
oborudovaniya (Kharikov Diesel Electric Locomotive Equipment
Works) together with LIIZhT, installed two prototype three-stage
amplidynes on a diesel-electric locomotive type -T.43-028
(TE3-028); they gave generally satisfactory test results though
they had certain defects. Since 1958 LIIZhT has been working on
Card 1/4

Some methods of improving amplidyne ... s/196/62/000/004/022/023
E194/E155
improvement of the amplidynes and investigated the following
problems-. selection of best number of amplification cascades in
the amplidyne, frame construction; location of field windings,
and selection of winding parameters. In order to seler-t the
optimum number of amplification cascades, tests were made on a
particular 45 kW machine connected both as a two- and as a three-
stage amplifier. It was found that the power amplification
factor of a three-stage amplifier is four times greater than
that of a two-stage. The maximum rate of voltage increase on
the terminals of a three-stage amplifier is five times, and the
average rate is three times greater than on a two-stage.
Moreover, the circuit of a three-stage amplifier is considerably
simpler. The tests showed that the use of a solid frame in a
three-stage amplifier almost halved its speed as compared with a
laminated frame so that the solid frame is disadvantageous even
though it is somewhat smaller. Two variants of amplidyne field
winding arrangement were examined and it was found that the
se~~ond variant, in which the amplifier and self-excitation
windings are mounted only on two poles, is better than the first
Card 2/ 4

Some methods of improving amplidyne.. s/196/62/000/004/022/023
E194/E15.5
':,'ariant in which they are located on all four main poles, because
this gives a smaller machine and the inter-turn connections are
much simpler. However, when the amplifying windings are located
only on two poles, the magnetic flux under the interpoles is
distorted (the output voltage on the amplidyne terminals is
reduced by 8-lo% compared with the first variant) and this must
be allowed for in designing the windings. In determining the
optimum field winding parameters, the main requirements are high
amplification factor and maximum speed for a giveri control power
Investigations to this end were based on the position of the
static_ and transient conditions of a three-stage amplidyne with
constant input signal appli,3d to the control winding. Moreover,
tests were made with variable control signals and constant
amplifier output voltage. The dynamic properties of the
amplifier cascades were assessed from oscillograms of voltage
increase, both separately from the second cascade and using the
complete amplidyne circuit. As a result it was found that the
speed of the second cascade is much reduced on introducing
premagnetising windings, and this naturally reduces the output
Card 3/4

Some methods of improving amplidyne ... s/196/62/000/004/022/023
E194/EI55
speed of the amplifier. Consequently, it is inadvisable to use
premagnetisation in the second cascade of a three--stage amplidyne,
A series of oscillograms was worked out to determine the relation-
ship between the maximum rate of voltage in--rease on the
amplifier output and the variable parameters of the amplifier
winding, and from these it was possible to determine the best
parameters (number of turns) of the amplif'ier winding of this
amplidyne. All these results were used in designing a new
amplidyne which will be used to excite the main generator of a
diesel electric locomotive. The circuit, dimensions, load
zharacteristics and voltage oscillograms are gIven for the
amplidyne with two variants of winding arrangement. Relation-
ships are expressed for the maximum rate of voltage increase of
the siDcond rascade and the number of turns of the premagnetising
winding and also for the maximum rate of voltage rise on the
amplidyne output and the number of turns in the amplifier
winding.
I fisure5, I literature reference.
Card 4/4, [Abstra--tors note: Complete +,ranslation.l
.1

BOLDTREV, G.P.
Technological study and estimation of iron ore deposits in
prospecting. Razved. i okh. nedr 29 no.9:10-17 S 163.
(MIRA 16:10)
1. Vsesoyuznyy nauchno-issledovatellskiy i proyektnyy institut
mekhanicheskoy obrabotki poleznykh iskopayemykh.

13 L 9
POSPELOV, G.L., starshiy nauchnyy sotradnik; LAPIN, S.S.; BELOUS, N.Kh.;
KLYAROVSKIY, V.M.; KINE, O.G.; VAKHRUSHEV, V.I.; SHAPIRO, I.S.,
stershiy nauchnyy sotrudnik; KALUGIN, A.S.; XMIN, A.S.; GARNWS,
N.A.; MITT, Tu.A.; SELIVESTROVA, M.I.; RUTKEVIbH, V.G.,-BYKOV, G.r.;
NIKONOV, N.I.; tAKOVICH, K.G.; MYEDKOY. V.I.; ALADYSHKIN, A.S.;
PAN, F.Ya.; RUSANOV, M.G.; YAZBUTIS, E.A.; ROZHDESTVENSKIY, Yu.V.;
SIVITSKIY. G.Te.; PRODANCHUK, A.D.; LYSENKO, P.A.; LXBxizv, T.I.;
KAMSYAVL, T.Ya.-, MASLENNIKOV, A.I.-. PIPAR, R.-, DODIN, A.L.;
MITROPOLISKIY, A.S.; LUKIN, V.A.; ZIMIN, S.S.: KOREL', V.G.;
DERBIKOV. I.V.; BARDIN, I.P.. akademik, nauchnyy ivd.; GORBACHEV.
T.F., nnuchnyy red.; YERCFEYEV, N.A., nauchnyy red.; NEKRASOV, N.N.,
nauchnyy red.; SKOBNIKOV, M.L., nauchnyy red.; SMITMOV-VARIN, S.S.,
nauchnyy red. EdeceaBed]; MUMILIN, S.G., akademik, nauchnyy red.;
NIKOV, V.B.. nauchnyy red.; CHINAEAL, N.A., nauchnyy red.;
G
SMZYUK, F.Ye., red.toms; SOKOLOV, G.A., red.toma;
G.'
red.; VOGMAN, D.A., red.; KASATKIN, P.F., red.; KUDASHEVA.,
red.izd-va; KUZIMIN, I.F., tekhn.red.
[Iron-ore deposits of the Altai-Sayan region] Zhelezortidnyo mesto-
rozhdeniia Altse-Saianakoi gornoi oblasti. Vol.l.' Book 1. [Geology]
(Continued on next card)

POSMOV, G.L,--(Gontinued) Card 2.
Geologiia. Otvatstvannyi red. I.P. Bardin. Moskva. 1958. 330 p.
(MIRA 12:2)
1. Akademiya nauk SSSR. Mezhduvedomstvenneya'pogtoyannays komissiya po
zhelezu, 2. Postoyawaya. mezhduvedomstvannaya komisaiya po zhelezu
Akademii nauk SSSR (for Pospelov, Shapiro, Sokolov). 3. Zapadno-
Sibirskiy filial Akademii nauk SSSR (for VakhrusheviPospelov.) 4.Zapadno-
Sibirskoye geologicheskoye upravleniye (for Sakovich). 5. Krasnoyarskoye
geologichaskoye upravleniya (for Pan). 6. Zapadno-Sibirakiy geologo-
razvedochn.yy treat Chermstrazvedka (for Prodanchuk). 7. Sibirskiy geo-
fizicheskiy trest, (for Pipar). B. Vaesoyuznyy geologicheskiy nauchno-
issledovatellskiy institut (for Dodin). 9. Gornaya ekspeditsiya (for
Mitropollskiy). 10. Gornoye upravleniye Kuznetskogo metallurg.kombinsta
(for Lukin). 11. Tomakly -politekhnicheskiy institut (for Zimin). 12. Si-
bir8kiy metallurg.institut (for Korell). 13. Trest Sibneftegeofizika (for
Berbikov). (Altai Mountains--Iron ores) (Sayan Mountains--Iron ores)

BOUTRE'vi-G.- P.; VOGMAH, D.A.; NOVGKHAT~XIT. I.P.; YERK, D.L.; DYUGATKV,
I.V.; KAVU11, V.M.; KURRUKO. A.A.: UZBXKOV, M.R.; ARSENITEV,
S.Ta.; TEGORKIN. A.N.;Xa1UKCY, P.F.; KUZIMIN, V.N.; STRMTS.
B.A.; PATKOVSKIT, A.B.; BOLESLAVSKATA, B.M.; DMBOH, D.B.;
FINKIMISMTN. A.B.; SHAPIRO, I.S.; LAPIN, L.Tu.. Prinimali
uchastiye: NEVSKAYA, G.I.; FEDOSETEV. V.A.; KASPILOVSKIT. Ta.B.,
M- OVA. K.V.. BARDIN, I.P.. akademik, otv.red.; SATPAUV, K.I..
skademik, nauchnyy red,; SMUMILIN, akademik. nau--hnyy red.;
ANTIPOV, M.I., nauchnyy red.; BELTANCHIKOV, K.P., nauchnyy red.;
nMOFBYBV, B.H., nauchnyy r6d.; KALGANCV, M.I., nauchnyy red.;
SMRIN, A.M., nauchnyy red.; GLMTUK, P.Te., nauchnyy red.;
VWX NIKOV, V.B.. nauchn" red.; STREYS, N.A.. nauchnyy red.;
BANKVITSER, A.L., red.izd-va; POLTAKOVA, T.V., tekhn.red.
[Iron ore deposits in central Kazakhstan and ways for their
utilization] Zhelezorudnye mestorozhdeniia TSentrallnogo Kazakh-
stana i puti ikh ispollmovaniia. Otvetatvennyi red. I.P.Bardin.
Moskva, 196o. 556 p. (MMA 13:4)
1. Akademiya nauk SSSR. Mezhduvedomstvennaya postoyannaya
komissiya po zhelezu. 2. Gosudarstvennyy institut po proyektirovaniyu
gornykh predpriyatiy zhelezorudnoy i mnrgantBevoy promyshlennosti i
promyshlennoeti nometallichaskikh iskopayemykh (Giproruda) (for
Boldyrev, Vogman, Arsenlyev, Yegorkin, Korsakov, KuzImin, Strelets,
(Continued on next card)

BOLDY)IRV. G.P.--(contlnued). Card 2.
3. Institut geologichaskikh nauk AN Kazakhskoy SBR (for llovokhatskciy).
4. TSentralino-Kazakhptanskoye geologichaskoye upravleniye Ministerst-
va geologii i okhrany'nodr SSSR (for Verk, Dyugayev, Kavun, Kurenko,
Uzbekov). 5. Nauchno-tssledovatel'Bkiy inatitut meldianichaskoy ob-
rabotki polaznykh iskppaysmykh (Kikhanobr) (for Patkovskiy). 6. Gosu-
darstvennyy tnatitut proyektirovaniya metallurg.zavodov (Gipromz) (for
Boleslavskaya, Indenbom. Finkellahteyn, Nevsk-gya. Fedoseyev, Karpl-
lovskiy). 7. Mezhduve4omstvennaya postoyannayn komissiya po zhelezu
AN SSSR (for Shapiro. Zernove's Kalganov). 8. Goeplan SSSR (for Lapin).
(Kazakhstan--Iron ores)

POLIKhRPOV, V., kand.okon.nauk; BOIJ)YREV, I., Imnd.ekon.nauk
Planning villages in Sol I.stroi. 14 no-5:
4-6 My ,59. (MIRA 12.'8)
(Talovaya District--City planning)

a L-1 -I.- A 1. a it OF .9 a no Et 6
ir:
0 St 2 Prepa"I ore for chlorination. I.G.Boi dvrev. Ru-
%Jay 3t, 1918. The ote is mixed -with crud-it
00 ).~tjvtn% and thrnroked.
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9000040060606000000000 #000900000060400000:

sov/68-58-11-9/25
AUTHORS: Boldyrev I.K., Gutman L.M. and Khurin S.M.
-1
TITLE: x-p-b-ftence-in Replwing' Gas-Air Valves and Increasing
the Travel- of the .. Reversing Equipment (Opyt zameny
gazovozdushny1ch k1apanov i udlineniya khoda kantovki)
PERIODICAL: Koks i lQiimiya, 1958, Nr 117 pp 2~-20' (USSR)
ABSTRACT: The method adopted for exchanging gas and air valves of
an old design for new,ones of a standard design and
...increasing the pitch of reversing equipment is described
and illustrated.
There are 4 figures.
ASSOCIATION: Stalinskiy Koksokhimicheskiy zavod (Stalino Coke By-Product
Plant)
Card 1/1

SEID-ZADEp._Q.-D. (Baku)j BOLDYREV, I.T. (Baku)
Gas pipeline at the bottom of the sea. Stroi.truboprov. 9 no.2:
21 F 164, (MIRA 170)

I I
Y.V., BOLDY,1101, 1.7l.; 'i.*"Z.
Lliphatl~,~ - arurriabic eston. c,.," curbx-,rilc a-id. Irkr. kh]j%. zilur.
1
50 no-12-1330-,1-332 2 64.
1. Inotitut lh-,*.Pdi jT blrSSR.

BOLDYFLEV, Konstantin Yiatveevich.
BOLDYREV, Konstantin Yatveevich. Navigation fishing vessels; approved as a text-
book for higher technical schools of the fishing industry. Moskva, Pishchepromizdat,
1946. 255 p. (50-26897) VK555. B72

STEFANOV, V.Ye.; AWYREV, L.I.
j4~i
Improving the fittings of large section and rsil rolling mills.
Metallurg no.8:26-28 Ag 156. (MA 9:10)
I.Kalibrovshchik krupnosortnogo teekha savoda "Azavstall" (for
Stefnnov). 2.6tarshly master stnna zavoda, "ArovstRl'" (for Bol"v).
(Rolling mills)

UTHUIL5: BolclyreV L I - kzenior i-oreman oi- -une iuwge 5ou-,i-a z5uvpj --
Central Works Laboratory).
ineer
search En
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.
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j
'30-3_16L22
ITLE. Organization of roll changing on a 650-mill~ (Orga zats 1 V a
perevalok na stane 650.)
BRIODICAL.- "Metallurs" (Metallurgist), 1957, No-3, pp.31-33. (U.S.S'.R.).
BSTRACT: The finishing line of the 650-mill at the Azovstall Works
consists of two three-high stands and one two-high stand arranged
in one, lineg the maximal diameter of the working rolls being
680 mm'. The mill rolls two types of rail-, I-section girders.,
channels ' squares-,.large angles and other sections. The senior
mill foremang V,D'. Krishtofovich has organized his roll-changing
team so effectively that the roll-changing time has been reduced
by 7'minutes. Details of the organization are given in this
article. Krishtofovich pays great attention to the preliminary
preparation of stands and rolls, the correct positioning of
roll-men and mill oprators, the rational utilization of cranes,
and maintenance of the sequence-of operations. It is considerel
Car". that the adoption by other teams of these organizatioml methoLs
would enable mill productivity to be increased by 2 - 3%.
There are two diagrams and one photograph.
,SSOCIATIO'N*. "Azovstall" Works (Zavod "Azovstall").
,VAILABLE.-

FROTASOV, N.F.; B141KOV, V.P.; SIKORSKIY, A.I.; GONCH&R. V-V-; DOLDYRIV, L.I.;
STICFANOV,- V-Ye- ---- --- %----.--.,',0.-j:--- i
DBveloping shapes for mine supports. Metallurg 3 no.12:27-29 D '58.
(HIRA 11:12)
I.Zavod "Azovetall.."
(Rolling (Metalwork))!
i

SOV/133-58-8-29/30
AUTHORS: Turchenkova, Ye.K.,Sikorskiy, A.I., Yegnus, R.1%,
Boldyrev, L.I , Raznotina, Ye.T., Engineers, Bollshakov,
'~Li iaMte of Technical Science"
i~. s,/ and Gavrikov, V.Z. ,
Engineer
TITLE: Performance of the Coupling Sleeves Made From Nodular Iron
at the Mill 650 (Rabota. soyedinitellnykh muft iz chuguna
s sharovidnvm grafitom na stane 650)
PERIODICAL: Stall, 1958, nr 8, pp 763 - ?66 (USSR)
ABSTRACT: As the durability of the couplinG sleeves of the mill 650
made from grey iron decreased with increased degree of
reduction per pass introduced in the rolling practice, the
use of sleeves made from nodular iron was investigated.
Four series of experimental smelting of magnesium-inoculated
iron were carried out. Sleeves from the first series
were tested as cast and of the remaining series after
various heat treatments. The chemical composition,
mechanical and conditions of thermal treatment are given
in Table Z The microstructure of heat-treated metal
- Figures 1-3, the mould for casting of sleeves - Figure 4,
the results of service life of sleeves made from nodular
iron, grey iron and steel - Table 2. On the basis of the
Cardl/2 results obtained, it is concluded that the service life

OV/133-5'-8-29/30
c'
Performance of the CouplinG Sleeves Made from iiodl.).laz Iron at the
Mill 650
of sleeves from nodular iron JLs 4-6 times lii-~her than that
of sleeves made from Crey iron. The optimum heat 8reatment
is normalisation vith subsequent annoaling at 580 C.
Sleeves should be cast witli the consumption of met-al for
shrinkage head not less than 2001o' of the r!eight of castinG- .
When coupling sleeves are not heat-treated, then the sum
of 0 + Si in nodular iron should be maintained in a range
of 5. 5-6, 01016. There are 5 figures and 2 lables.
ASSOCIATIORS: Zhdanovskiy metallurgicheskiy institut (Zhdanov
Metallurgical Institute) and Zavod "Azovstall"
("Azovstal'" Works)
Card 2/2 1. Couplings--Materials 2. Couplings--Test results
3. Iron--Applications 4. Steel--Applications

suv/13U-58-10-9/18
AUTHORS: Protasov,'N.F., Khlebnikov, V.P., Sikorskiy, A.I.,
Gonchar, V.V., Stefanov, V.Ye and. Boldyrev, L.I.
TITLE: Improving Accessories on the Reducing Mill of a Heavy-
Section Mill (Usovershenstvovaniye armatury obzhirnnogo
stana krupnosortnogo tsekha).
PERIODICALt Metallurg, 1958, Nr.10, pp.25-29 (USSR)
ABSTRACT: It was found that when rolling low-number girders,
especially Nr.20 in the reducing stand of a rail-
structural mill the metal often displaced the guides,
leading to stoppages. The authors give details of guide
construction and attachment (Fig.1) and also of special
devices provided before each pass (Fig.2) to support
the beam from below. This is advantageous for rolling
large girders (Nr.30-55) but unreliable for smaller
(Nr.18-16) sizes. For rolling these latter when the
closed passes are in the bottom roll two variants of
guide arrangements have been proposed. In the first
special movable vertical supports are provided for the
Gard 1/2 guides, fixed on trapezoidal projections. In the

SOV/130-5B-10-9/18
Ii~proving Accessories on the Reducing Mill of a Heavy-Section Mill.
second a trapezoidal-section bar is fixed to the housing
(similar to the guide bars on the finishing line) (Fig.4)
which supports one end of the specially shaped guide, the
other being held in the pass with the aid of a load. The
authors favour the second variant and mention its
applicabilities. Its adoption has enabled the load
on the finishing line to be reduced by 20-25%. The new
roll-pass designs used since March 1957 have led to better
roll life, higher productivity and other improvements.
The new accessories are especially useful for thin-walled
sections,and during the year for which they have been in
use no cases of guide displacement have occurred. There
are 4 figures.
ASSOCIATION: Zavod "Azovstall" ("Azovstall" works).
Card 2/2

SOV/130-58-12-12/21
AUTHORS: Protasov7 N.F., Khlebnikov7 V.P.7 Sikorskdy, A.I.,
Gonchar, V.V *, Boldyrev, L.I. and Stefanov7 V.Ye.
TITLE: Experience of the A ~dp '~o profiles for Mine Supports
(Opyt osvoyeniya profiley dlya shakhtnogo e:repleniya)
PERIODICAL: Metallurg, 19587 Nr 12, pp 27 - 29 (USSR)
ABSTRACT: The "Azovstall" works is one of the main suppliers of the
more important sections for mine construction and opera-
tion. The authors illustrate (Fig 1) sections for props
types 18A-18B and 28A-28B and show how the first two fit
each other (Fig 2). These sections are rolled from
230 x 285 and 21+5 x 280 mm. blooms in four stands arranged
in two lines and the authors outline the pass design and
deformations at the various stages. They deal with the
production of inclined props to GOST-5157-53. The authors
Card 1/2

SOV/130-58-12-12/21
I
Experience of the Adoption of Profiles for Eine Supports
state that the pass designs for pit props developod at
the works have improved quality as well as increasing
production.
There are LF figures
ASSOCIATION: "Azovstal'" works
Card 2/2

AUTHORS: Boldyrev, L.V. , Krasnosel'skiy, Y.V. , Rudnev, 1.7'. 131 -3-2/16
TITLE: The Increase of 'he Efficiency of Shaft Furnaces '.'i-ith Gas Heating
(Po,~-Ysheniye proizvoaitel'nosti shakhtnykh, pechey r-- ga--c%,on
otoplenii)
PERIODICAL: Ogneurory, 1958? Vol 23, Nr 3, rp 101-105 (USSR)
ABSTRACT: At the Semiluld Plant for Refractories it was possible, by iin-
proving the construction of furnaces and of the burning process,
to increase the daily out-put from 25-40 t to 65-770 t.
I.A. Savkevich assisted in this work. The auth~-,rs further describe
the constructior. of the furnaces as ;,,rell as the worlring process in
detail. The revolving grate is shoym in the illustration and its
useful cress section is given by table 1. At present the buridng
process takes place as follows: 1.) The pr&-paration of clay for
burning. The clay is crushed by means of a machine and is formed in-
t~ briquettes of I kg weight and shaped like flattened balls
(0 120 and 90 rm.). The quality of the clay and of the briquettes is
continually controlled. 2.) Charging and discharging of the furnace.
Every furnace is discharged in the course of each working shift
according to the temperature of burning, of the material -aith which
Card 1/. 2 the furnace is filled, and the moist-ure content of the lbriq:uettes.

The Increase of the Efficiency of Shaft Furnaces 1 _3 -3-~l 16
With Gas Heating
In accordance -.4th the work to be perfo=,ed the control apparatus
KXT-3 are adjusted, by means of which the charging dru:ro are con-
trolled (table 2). They ar-i bloOked by means of an electron zdili_
volt meter which continuvasly controls -the exhaust gases and which
switches the control apparzatws on or out according to necessity.
DiscInarging of the furnace takes place in dependence of charging
the furnace in order that a constant level of material be main-
tained- 3.) Gas- and air supply is detennined according to con-
suir.rptior. per hour, regulation being carried out according to burners.
4.) Control of furnace work. In the shaft furnaces of the Semiluksk
works the follovang measurement3 are continuously carried out: Gas
consuwtioa, temperature of exhaust gases, temperature of the mate-
rial in the furnace, furnace pressure and "he level of material in
the furnace. Besides, the temperature of the discharging fireclay
bricks and their quality is continuously controlled. Table 3 con-
tains the working data of shaft furnaces for the years 1950-1957.
Thexe are 3 tables, 1 figure, and 4 Soviet references
ASSOCLAMON: Semiluki Plant for Refractories (SemilukFA-11Y Ogaeupornyy zavod)
1. Gas burning furnaces-Operation 2. Furnaces-USSR 3. Refractoi7
materials-Processing 4. Refractory materials-Production
Card 2/2

ACCESSION NR:, APS0132.69
`d' cribedo A,tr=13toarcit,mbdolgeowpiricallV,airnilar.-to the.combustion chambe'
es
and wor)dng with wad: used,for- investi-,
'g. I ese experime pernAtted i9 cti~igir tb~ design
~thig the swirli-bg pr6c,eq. r~ nts ele
d cvntipl,paranidt~rs -.161 the siviTler."'The-effectiof ~Zas,b*17Hing,-.Waa studied.,on
a few.(tivree?) hig&gpeed'~milrler-eqmpjped engiji6A,bnd6YVdki6UG cylinder -M.at-
exhauBt a ~turbidtty ured. It was,
6 case conditiami. the -;P. Was meav bound
that, under low air-fuel-ratio con diti ons-;- the ga ia swirUin,'r6iult~ in' ai c'o'iniisldder
able increase (3-SQ'In-the engine indic''ated power and in a lesser turbidity 4~f the
exhaust gas. In all -cases,., the effect. of swirling. 6 s ventially iiii~rcaqed with tbb
f f The Russian 1
ivai. (i. e. with the dbcrqasil~g air-fuel-ratio). Al~aradter a note.
original 6&bx the Plsch=bfiko~o 66me other typ or i
d Is nof clear as. to Wh e. of ~Wiri
-1 table.
was used in the diesni4hk~~Ak"tv-3 024~._ hta.-_-zT figims and
ASSOCIATIOTi~
D! .00, SUB CODE%*: PR
F so 0ov.
OTIMM
4T_'