PRODUCTION, EXPERIMENTATION AT THE BUNA-WERKE, SCHKOPAU
Document Type:
Collection:
Document Number (FOIA) /ESDN (CREST):
CIA-RDP82-00457R005100070009-3
Release Decision:
RIPPUB
Original Classification:
S
Document Page Count:
14
Document Creation Date:
December 14, 2016
Document Release Date:
March 26, 2003
Sequence Number:
9
Case Number:
Publication Date:
July 7, 1950
Content Type:
REPORT
File:
Attachment | Size |
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Body:
1 it- - ,
ELLIMI 4
Approved For Releas
COUNTRY
SUBJECT
PLACE
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DATE OF
INFO.
NHDEpiqq
57R0051000702M0
CLA5SIFICATION 0,7,Ceiat1
CENTRAL INTELLIGENCE AGENCY
IN FOR
It
g
Germany (Russian Zone)
TIO NI REPORT
REPORT NO.
CD NO.
25X1
51
DATE DISTR, 7 July 39)5.0
Productions Bxperimentation
NO. OF PAGES
14
at the Buna41(erke, Schkopeu
25X1A
01%
NO. OF ENOLS.
14tk (LISTED BELOW)
vs0
SUPPLEMENT TO
REPORT NO.
25X1
Witk,i,:41:
THIS VIOCOOSITT CONTSIO3111FORZ1147891111PRICTIOCITTIS VISITOLIAL DEPPITSE
OP MO ourrErs SsTATEa 131TO111 TUE 1333611NO OP TOE POPIOP4A011 OCT ZO
11. is.t at SOD E. RD 1112ENOTT4 113 VOSSOCIFratti1313 Ott TOO RINCLATTOB
OP In, COOTHOT3 113 11W1 cuismen TO SO OUSISTKORV230 venom: 13 POO.
t11131TOD OT
LMT. ISCPRODUCITOCI OF TOM POWS 13 P52011131530.
kkgr
'MEM. gt2044.',W=4,4.;,,AVO
25X1A
25X1
THIS IS UNEVALUATED INFORMATION
A copy of the 1,roviaionalort 2.122Liments to Improve
the 4ua1ities OT7Tum-inara:qxfaTTis Active77ETTeTTIII41
77o5Ft76-271T6F-MEET44a-746T the SchEaliargifirailaated
0 el7FairiTIMY?TE?Riaiiigided
Comment:
..--..amearaw.ammor.a.a.....ro
a. The Buna Plant in 6chkopau is assigned to the Kaustik
.ioviet Corporation and its production is partly combined in
the Leuna Picat schedule. Part of the plant was dismantled
in June. 1948. The following official 1949 prodwtion plan
provides for an annual buns pt.oduction of 27,000 tons. This
estimate is exagferated and w111 probably not be reached due
to the dismantling At present,the plant has the following estimated
rIual 7rodrctiOn capacity:
- Carbide 3003000 tons
--Nina S 3 203000 tons
-'Igelit Par 7,200 tons (polyvinylchloride)
Polystyrol 400 tons
t-Ethylene oxide 9,000 tons
Eutanol 3;600 tons
Trlhiorethylene 3,000 tons
ilethyl acetate)
?'-;Rthyl acetate) 8,000 tons
v-Lutyl acetate i
iicetone 2,400 tons
(zAcetic acid 143000 tors
vliormaldehyde 2,900 tons
Anhydride of plotalic acid 3,000 tons
,Chlorine 333000 tons
'"-Caustic soda 3,600 tons
:Aluminum chloride 7,000 tons
Lubricating oil 3,500 tons
Thie.....xlacuccua
comsffilivni
Director of Central td the
Archivist of the Uniteti CMOS,
Next Review Date; 12008
CONFIDENTIAL25xi
TION rariGEMY
?1 DISTRIBUTION
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(2)
DOnuTA
ApproveZIW Rejsmagicl3en4jj utrag00510
.2-
41).;.,oNriet mt3nagement personnel:
General munager: i'lazarov
Janager: Ratasov (Eng)
-lanager: ,Stolyazov (Eng)
Engineer G?olovin
Engineer Frityeff
aj Gomsharenko
Ge 1118.X1 rla nage rro nt Personnel*
0070009-3
nager Jr.% elles, chief of the plant -
?:Ic.nager Dr. Liar!
First engineer Savamach pr, chief of the - technical and
cons t ructi on section
Diplomkaufmann (academic dee;ree :of political economy)
Roehr, chief of the com7-
mercial and auditing section
f)Or
3. The report indicates the kind and trend of oxperi lents/the
improvement of the properties of aluminum oxide to be used
as active filling agent for rubber mixtures, The abbreviations
used in the tabulations are presumably to be explained as
follows 2
coefficient of strength
D. elongation
? 1)1D, permanent elongation
El. strain
H. hardness
'Teflannation. degree
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SOOMM
CENTRAL INTELLIGENCE AGENCY
-3-
2r9v s;Lonal Retort on 41Te,riments to Improve -.9 eualities of
tures
21.1uminum Oxide as Act ve Wh te itrent n Ru er-
----I, a
The eurpose of this -provisional rerort is to acluaint the
technical personnel of the plant with the results of exper.
:nefts made to find an improved aluminum oxide composition to
be used as active Main- arent hesearch activities are not
corepleted but the results achieved so far can be used as a
basic method in the manufacturinp procedure.
The first patent for the use of aluminum oxide as filling agent
as applied for in 1941 by the Deutsche Gold- un d edlberscholde-
anstalt Firm. In this application aluminum oxide was mentioned
as highly active fliling agent for natural and synthetic rubber0
Ely using aluminum oxide as the filling agent the tensile strength
of butadienerubber is increased to 208 kg/cm2 and the strength
limit is 462 percent.
In tests by Jr. Lelles and Die ilauschulz in the Luna plant
and tests by Jr, Pattok in the 2arbenfabri1 Tablfen, the ad-
dition of aluminum oxide (obtained from alum or aluminum eul-
phete) indicates an excessive degree of defornat1on (10,000
to 20,000 or more) although the soligity of the vulcanized
meterial is increased (200-2/30 kg/cm-)0
leabber mixtures with such a high deformation depree cannot be
processed in rubber plants. Therefore the industrial use of
aluminum oxide as an active filling agent was not practicable
in the form proposed by the Deutsche Gold- und oilberecheide-
anstelt
The value of eluminam oxide as filling material is also con-
siderably reduced due to its excessive static stretch dilation
(40 to 80 percent).
Dr, Hellos and Dr. Lauschulz made seecial tests to obtain
aluminum oxide with a normal rate of mixture deforezation0
email quantities of inorganic salts of alkali-metals and
other :letals were added to the sulphate before the beatine
process, The tests had no practical results. Illthoueh the
decree of deformation declined,the tensile strength of the
vulcanized material decreased .considerably.
5. It is probable that the addition of alkali-salts at a heat-
ing temperature of 9000 to 1,0000Cleads to the formation of
nonactivo meltines with aluminum oxide or favors sintering of
aluminum oxide particles due to their size or share or the
condition of the surface, thus producing nonactive forms.
exe Espich tried to solve the ?nroblen of the low degree of
dellormation by the same procedure, Aie also added various
Inorganic salts to the basic wew material before heatine.
However, his tests did not lead to any positive results
either,
The following data were listed in the experiments of Dr.
Ir,seich;
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CENTRAL INTELLIGENCE AGENCY
25X1A
Tf1,112e
Designation Zixture Heating F D.
of material degree
,aguawasz.v.,...,sp,a,,,neo.ax,d*asta.megalannewI*AMOIR*.
bl.D Lel
inaLIIIISie.1.4.0164,114%?-?
El
h
,ekixture ','t53f0
',mi., , ?
A1203, E-17
92 _
20v/2.1
138
520
55
71
49
68
6550/39 100 cm37
5 kg alum
40'
157
475
46
:87
50
70
18.6 g
and 687-16.5 g
60'
167
460
40
'99
50
70
HaC1
80'
160
435
33
103
50
71
e
100'
167
440
33
107
50
71
60v/3.0
174
465
34
109
.50
72
- _
_ _ _ _
01. ?Ai
?II, G., mu.
'.
OW
''' ''. 7,
A1203, L-16
92
20v/2.1
102
450
29
77
50
74.
6550/28 100 cm Y-
5 ic: alum
40'
98
360
20
67
50
75
24.2 g
and 68-16.5 g
60'
102
365
20
'91
50
76
fluoride
80'
101
335
17
93
50 .
77
100'
102
330
16
96
50
78
60v/3.0
99
325
15
93
50
76
_
E-19
92
20v/2.1
129
420
53
90
48
74
12050 36 100 cm?-
35 kg a1u-
40'
141
400
43
104
48
75
21.2 g
minum sul-
60?
149
385
41
112
48
76
phate
802
155
375
39
121
48
.76
100'
151
360
34
124
48
76
ao
aoa
60v/3.0
147
355
31
122
48
76
wa aro amo n.a a, .an
Al2.03, E-20
92 -
20v/2.1
97
455
22
71
53
74
5250/32 100 an6-
3.5 kg alu-
40'
98
405
19
79
53
74
25e5 g
minum sulphate
60'
96
390
18
80
54
75
C 37ga " liana
60'
101
395
18
63
54
75
-16/5 fluoride
100'
87
340
13
61
54
75
60'/5.0
91
360
14
80
53
75
a, .11. usa O.S MS oar a,
,a,weaarataTaxamaakavar,,araraaarra iI.T,V,G,Isa...01.,110, IRIVO.I...10-0,01.14-79G-401.1."1.-3.14,41311InIGIrn
SAG. NOIWGIts .
suf. I.". YON
Summarizing the mentioned tests aluminum
oxide is not suitable as a filling agent in the proposed
form, Hoveirer, the research is sipnificant as it proves
for the finet tiro, that the tensile strength of vulcanized
material Is considerably increased by adding to the rubbeA:
mixture aluminum oxide obtained from alum or aluminum sul-
phate through disintegration at high temperature. Aluminum
oxide can be used as active filling ogent in the rubber in-
dustry only after the problem of reducing the degree of de-
formation to a normal figure (1,500 to 3,000) has been solved.
ley reducing
of vulcanized
dilation coefficient
to solve this
the degree of deformation many other qualities
materials are also improved (stretch, stretch
and so on). Our research work was done
problem.
25X1
6,
Description
of aluminum
ofl laxpariments to improve the qualities
oxide.
the experiments of Dr lolles and Dr. Uauschulz
25X1
to achieve the reduction of the degree of raw
by processing the finished aluminum ,oxide mith
.eeorma on
organic substances and not by adding various inorganic sub-
stances to the raw material during aluminum oxide production.
a. The first method consists in adding softening agents to
the mixtures in order to obtain .a reduction of the degree of
deformation. For this purpose paraffinic acid as added to
the rubber mixture in quantities of 2, 3, 5, and 8 percent,
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CENTRAL INTELLIGENCE AGENCY
The results results .show that by pereent.of paraffinic acid
only a decrease o4. the degree of deformation occurred.
?hu addition of paviffinic acid in greater quantities leads to,
a reduction of the degree of deformation and to a reduction
01' the tensile strength of vulcanized material (see table 3).
This method was abandoned due to unsatisfactory results,
b. The second met'aod consisted in covering the surface of the
aluminum oxide with the layer of organic matter to decrease the
friction between rubber and filling agent. thus reducing the
degree of raw deformation. This represents an absolutely new
procedure in the rubber industry.
ehile examinin silipur as an active filling agent* obtained
through precipitation of silikosol sulphate by moans of an
ammoniacal. solution of sodium sulphate, Dr. Pattok tried
various materials to increase the moistening property of the
filling agent in tAe rubber compound. The following materials
were tested:
T.G. wet, chloric rubber, styrol, raw rubber,I,G, wax N (new)
and benzyl cellulose. These materials were first dissolved in
water or benzol and in this condition coated on the surface of
the filling agent. As shown by the table below the used ma-
terials not only reduced the degree of solidity but also in-
creased the decree of the deformation of the ray mixtures.
Filling
material
Silica gel pow..
der/ silipur not
processed
6i1ipur 636 with
IG wax suspension
Llilipur 636 with
chloric rubber
Oilipur 693 with
styrol solution
6ilipur 640 with
raw rubber
Silipur 642 Wth
IC; wax N
jilipur 644 with
benzyl cellulose
Table 2
Filling
welEht
Defo
13
5500
28
7050
25
9050
20
11050
25
8550
20
9550
21
9050
F
D
11.D
E
H
76
595
33
56
69
19
330
29
57
69
24
275
36
57
73
25
230
17
58
75
22
309
33
57
69
22
320
29
54
74
20
335
35
56
72
These. data show that the second method of solving the problem
was at first a failure.
(ettig?Crii-1:0=
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CENTRAL INTELLIGENCE AGENCY
-6-
c. At a meetincrpf.th the Chief ricineer General Kirpichnikov
in charge, first engineer Khcheyun suEcested, for the first
time, obtaining a low decree of deformation by submittinc
the finished alumiaum oxide to an additional process..
Tests were started to lower the decree of deforlation of
raw buna mixtures by processing aluminum oxide with organic
matters. A simple procedure consistinki: of an additional
treet'dent of A120R with. nekal B4made'in the laboratory
of Engineer ZacaaMas proved this method to be correct.
4ie?!era1 organic Sub.sikances were then used in later tests,
Description of the oxrerimental part.
_dixinc formula ik) 92
Euna S 3
Aluminum oxide
Zinc oxide
6ulphur
Vuikasit "A"
100 parts of weight
80 parts of weiFht
5 parts of weight
2 parts of weight
2 parts of weight
The aluminum oxide containing mixture is rolled 15 to 20
minutes without additional treatnent and 15 minutes
after treatment,
The test results obtained arter addition of 2 to 8 percent
of paraffinic avid to the mixture are listed in table No 3:
25X1A
Designation
of material
Alxture
heating
degree
3 . warmsrowneorwevian,a......xmvon=my,.:+75....?Ap
_ NI
Table 3
bl.D Bel, El. H.
M.,
,Axture Wel,oht
defo
F D
. v+r ...?. ,
Itta, ? Ntsi.V.X....r.VAIraN"
A1,0,7 from
92
20//2,1
153
455
65
95
50 78
above 100 .am3-
12,ittdrfeld
20000_ 80 g
40/
GO"
175
185
460
450
64
59
105
117
50 79
50 79
not
ticeable,
breaks
80/
208
455
58
:127
50 SO
100/
209
445
58
133
50 80
60//3.0
203
445
58
129
50 80
60//4.0
200
405
48
134
50 80
A. O. .?I??
A1203 from
_
92
20V2.1
289
189
-3S5-
590
AO
50
-128-
50- -so -
43 75
. C.CT)
16550/ 100 cm 5
Litterfeld
48 20g
2 Percent
paraffinic
acid
60/
215
235
555
555
46
44
86
96
43 70
43 78
80'
237
540
38
104
43 79
1001
259
525
38
110
44 79
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4=4,1E4Y
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CENTRAL INTELLIGENCE AGENCY
?7-
25X1A
7
60'/3.0
231
495
35
116
43
79
60'/4.0
215
MO
26
131
43
79
80'
224
445
28
133
43
79
A1203 from
92- W/2.1.175
640
50
61
42
72
12050/47 100 0113-
Li torfeld
3 ,o
20 e
1/.11.6.40'
191
605
42
68
42
74
CO'
199
505
39
75
42
74
80'
228
600
42
85
43
75
100'
226
575
38
89
43
75
60/3.0
224
545
37
89
42
75
60'/4.0
204
485
26
101
42
76
80'
213
440
24
118
42
76
A143 from
92- 201/2.1
175
705
45
38
42
69
6050/35 100 ams:
Litterfold
5 %
20 g
i.F.S.401
182
650
39
49
72
71
60'
171
610
34
52
42
71
00'
183
610
36
54
43
72
100'
184
610
33
56
43
74
60'/3.0
176
590
33
58
42
74
601/4.0
167
565
29
58
42
76
00'
206
565
29
63
42
76
A1203 from
92- 20'/2.1
90
331
100
2000/31 100 om3-
iAtterfeld
6
20 g
3.F.3.401
88
545
14
28
42
62
60'
94
515
13
34
42
64
eot
94
490
12
36
42
65
100'
106
515
14
36
42
65
601/3.0
90
510
13
35
42
65
601/4.0
126
575
16
32
42
64
801
121
575
15
31
42
65
Atiiiinteick^
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Imcnmri
CENTRAL INTELLIGENCE AGENCY
-8-
1?inal conclusions
.additions of 2 to 3 percent of paraffinic acid increase the
solidity up to 250 kg/cm2; they improve the ductility
decrease plasticity,and.slightly reduce the decree or de7
formktion.
After addition of 5 percent of paraffinic acid the tensile
strength ?decreases, the ductility improves, and the-, .
degree of deformation declines considerably but not enouch.
3.
further addition of paraffinic acid nroduces a sharp decline
of the solidity of the vulcanized material. The degree of
deforMation remains normal.
. The second test series investigated the treatnent of aluminum
oxide with actents to imnrove the mixing nronerties of the
filling agent with rubber. Those tests were based on the fol-
lowing procedure:
olutions of vani
prepared. Alter,
vents, aluminum
for 2 to 3 hours.
at a temperature
of the solvent).
ready for use,
ous concentrations of the test material are
methanol, benzolpand xylol are used as sol-
oxide is poured into the solution and stirred
The solution is then filtered and dried
of 70 to 105q0(depending on the baling point
4ifter this processythe aluminum oxide is
The test results are listed in the following charts:
Table 14o 4
25X1A
Designation
idixture Heating F
(o0)
D
bl.D Lel. El.
H.
Aixture Weight
defo
Al203 from
bitterfeld
without
treatnent
92
40'/2.1
60'
175
189
460
450
64
59
105
117
550
50
79
79
not no-
ticeable,
breaks
80'
208
455
58
127
50
80
100'
209
445
58
133
50
80
- -
A120.7, from
92
40%/2.1
108
605
35
33
45
68
34A0/30
Littgrfeld
processed
with 2-;0
solvent
60'
60'
119
122
.615
610
35
35
34
34
45
47
66
66
L-1000
100"
117
590
30
36
47
66
Alt, 0 r3 from
92
40',/2.1
100
745
21
16
43
58
2400/29
Eitterfeld
processed
with 5-
solvent
60'
BO'
119
126
750
735
23
21
16
19
44
44
59
60
11;-1000
100'
100
685
20
19
44
60
..7711:31a4.41.
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AtenETA
CENTRAL INTELLIGENCE AGENCY
_9.
A143 from
Litterfeld
92
40/2.1
processed
with 10-;.;
solvent
60'
80'
121
251
2,-1000
100
147
a
a
a @
a
A1203 from
92
401/2.1
207
Literfeld
processed
60'
221
'with 1-,)
Sepal*
solvant
80'
218
1001
2-2
A1203 from
92
401/2.1
131
Bit terfeld
processed
with 3-%
60'
141
6opa1 so1-
vent*
80'
128
100'
126
A1203 from
92
40"/21
91
Bit terfeld
processed
with 10-%
601
105
Sapal sol-
vent*
80'
96 ?
100'
90
Al 0 from
2 3 '
LittOrfeld
processed
with
92
40'/2.1
204
200
Seral
vent**
80'
219.
100'
215
A1203 from
92
40/2.1
209
Litterfeld
processed
with 3-,0
60'
213
Jeral sol-
vent*
80'
201
100'
234
Al2.03 from
92
401/2.1
224
Litterfeld
processed
with 5-,o
60'
209
6era1 sol-
vent**
80'
235
100'
235
not vulcanized
775 43
730 41
680 37
530 61
520 62
530 56
540 62
715 40
690 40
650 34
650 36
685 27
660 26
610 24
615 24
680 45
640 39
650 42
630 56
OF a
750 37
730 39
660 2$
695 31
770 36
720 30
715 29
695 28
OaaWailDiaa@aTa,
25X1A
28
34
36
43
43
43
65
68
69
@ WO
2050/31
OFs r
@
a
a
103
46
74
13000/48
114
46
75
108
46
75
109
46
76
a
WIT.
4*
a
31
49
65
'4000/25
33
49
66
36
49
68
35
49
65
le.
19
47
60
1900/27
22
48
61
94
50
61
24
50
61
ma
a
58
43
69
0550/4].
60
43
71
62
43
71
04
44
71
O.
F. AM
44
39
67
7050/36
45
39
70
52
39
70
51
40
73
37
36
68
4800/39
38
38
66
41
36
66
43
38
66
Sepal oxalthylated alkylphenol
Seral oxalthylated paraffinic ,acid C12-044
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-10-
.0.203 from
bitterfeld
processed
with
benzol
acid
solution
92
40Y2/1
60
80'
100'
232
235
235
241
760
725
730
710
41
36
36
32
42
45
48
46
31
31
31
31
71
72
72
72
6150/36
A1203 from
92
40'/2.1
149
655
18
27
47
66
3700/28
Li terfeld
processed with
60,
168
650
17
30
47
66
1-50
solution
80'
176
645
16
34
47
68
100'
175
610
15
37
47
68
A1200 from
biltorfold
processed vitt)
92
40?/2.1
60'
168
160
815
745
40
37
24
28
45
45
61
64
2050/33
solution
80'
173
735
35
31
45
65
100'
200
745
38
31
45
65
A1,0,-4 from
92
409/2.1
207
710
56
51
46
70
7550/37
Iii%thrfeld
processed with
60'
200
690
55
51
46
71
..iersolat
solution
80'
205
675
51
58
46
71
100'
215
665
51
62
46
71
,gat
IVO RIOS
A1203 from
92
40'/2.1
211
750
68
47
42
69
5050/30
Litterfeld
processed with
60'
194
730
68
44
42
70
.ders lat
solution
80'
219
735
68
51
42
70
100'
212
715
65
53
42
70
A1203 from Lit- 92
terfeld, pro-
cessed with
40,/2.1
60'
186
200
730
730
35
35
28
28
43
43
60
al
1450/29
:.iersolat
solution
eco
200
720
33
31
45
61
100'
186
705
30
31
44
61
AlpO3 from
bi terfeld
processed with
sodium re-
sinate solution
92
40'/2.1
60'
801
2Z"5
279
246
810
765
720
62
60
52
45
53
57
38
38
38
72
75
76
4700/40
100'
300
740
49
60
34
76
ca&lettwir's
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teNCILET-7
CENTRAL INTELLIGENCE AGENCY
-11-
5
25X1A
*
A1203 from 92
40'/2.1
264 770
32
31
30
63
1900/30
Di tcrfeld
brrJessed with
60'
254 750
28
33
38
63
ferro-
naphtate
solution
00'
254 740
27
37
38
65
100'
225 710
25
32
38
85
.196 .... .............
..
*0011,LIMMMINM.IMOM
Table No 5
A1,0m from 92
hi%Orfeld
not processed
40'/2.1
60'
235 540
230 515
55
47
104
111
44
43
74
75
18550/54
80'
250 520
46
121
43
76
100'
250 515
42
122
43
78
A1203 from 92
40'/2.1
240 710
47
50
37
74
4550/21
Di torfeld
processed
with sodium-
resinate
solution
60'
80'
230 675
246 675
47
46
53
57
37
37
74
74
100'
275 655
46
69
37
75
A1203 from 92
40'/2.1
168 535
87
80
48
73
9550/35
Litterfeld
processed
with naphts,-
lene-sulfo-
acid sodium
60'
80'
167 515
168 500
75
71
84
89
48
48
73
74
100'
173 485
62
96
46
75
A1203 from 92
40'/2.1
122 1125
100
18
29
65
3900/25
Litterfeld
processed
with so-
lution of benzol
sulfonic acid
60'
80/
171 1030
180 955
84
65
24
26
29
29
65
69
100'
188 295
63
29
30
71
A1203 from 92
40'/2.1
240 710
34
38
35
GO
25C0/37
Litterfeld
processed
with solution
of naphthene
acid
60'
80'
225 675
226 670
31
30
40
40
35
35
66
66
100'
220 645
28
43
35
66
4.?
M.
A1203 from 92
40'/2.1
130 810
42
26
42
64
2100/28
Eitterfeld
processed
with Ueliko-
noel solution
60'
80'
157 765
154 730
42
38
31
32
43
43
65
65
100'
144 700
35
35
44
65
......... ........
woo am os.
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-12-
25X1A
wasaaaaangaaskaaanerataprrngraala*
alartaaraaavaa*a aanalandsa aaalaaaaaawaa aaakaanaaaalialeataar llanarralataa
6
8
its aka acallair lam
ayamsaleamaaaaralaaa.a.maa. - airaa.aaa.vaaarSia
A1,03 from 92 40'/2.1
119
050
46
--4 ryA
,,
52
64
2700/14
Littorfeld
processed 60'
with Zephirol
solution* 801
123
105
630
505
42
38
27
27
53
54
65
65
100'
102
555
35
30
54
00
_________ .. .? 4. 0110
mw VT
???
S. lA?
al al
a?
.."
.a
. ?
tak
al a, ta?
A1203 from 92 401/2.1
177
750
35
25
44
60
2200/30
Lirterfeld
Llersolat 60'
washed 5
times with 80'
165
200
700
705
32
32
28
31
44
44
61
62
1120
100'
185
095
32
32
44
62
a.. leAlk are .1 ?
,710.101.91.1.44.1. ep...t.,...elvaa.V.w04,1 .Vol.11.07M.15,11
Table ii2q.-
Exneriments to .TirTyprove the .Glasticity of Rubber
......olOkosaereo....ronnwertvnarnummoommac
A1,03 from
92**
4D'/2.1
210
715
45
42
40 .
70
3500/31
Bitterfeld
processed
with sodium
resinate
solution
60'
80'
226
264
630
700
43
47
50
54
40
42
71
72
100'
255
670
43
57
42
73
Al 03from
92***
40'/2.1
191
670
38
39
42
70
3250/25
Li-Lterfeld
processed
with 2-5
sodium re-
sinate
solution
GDP:
80'
100'
222
234
23'7
705
685
650
39
39
38
44
44
51
42
42
43
70
72
72
A1203 from
92
40'/2.1
154
960
65
19
51
60
3000/40
Litterfeld
processed
with 2-1
60'
183
865
55
27
51
? 63
Oleic-acid
solution
80'
210
860
45
29
51
64
100'
222
855
43
30
51
64
4-4
***
Zephirol -?:lixture of akyl-dimethylbenzyl-ammoniachloride
of great molecular weight
The contents of aluminum oxide elements (as A100,) in the
rubber mixture is 70 percent instead of 80 pe/teht as stated
in mixture formula Wo 22.
The contents of aluminum oxide elements (as A1203) in the
rubber mixture is 65 percent.
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CENTRAL
INTELLIGENCE AGEN CY
-13-
Al 03 from
92
40'/2.1
176
680
26
29
52
64
1600/22
Bitterfeld
processed
with 3-;.,
oleic-acid
solution
60'
80'
195
200
655
660
25
24
32
30
52
52
64
65
100'
185
050
24
36
52
65
X1203 from
92
40'/2.1
190
765
36
27
45
65
2200/28
Bitterfeld,
processed
with 2,-.0
linoleic
acid solution
60'
80'
180
200
725
735
34
37
28
31
45
46
66
67
100'
200
725
30
34
47
68
---
- 140
x1203 from
92
401/2.1
156
790
52
29
47
66
2750/26
Litterfeld
processed
with 2-%
solution of
60'
80'
160
180
760
755
47
46
30
37
48
48
67
69
sodium-
oleat
100'
200
740
45
36
48
69
A1203 from
92
401/2.1
200
720
53
40
46
68
3800/30
Bitterfeld,
processed
with 24.)
solution of
60'
80'
197
210
720
675
52
49
41
48
46
47
69
70
sodium-
linoleat
100'
200
650
45
50
48
71
25X1A
9. Conclusions of Abovelisted Tests
a. The processing of aluminum oxide with various agents diminishes
friction between rubber particles and the oxide surface
produces a filling agent riving rubber a high rate of solidity
(280-300 kg/cm), and tensile strength (000-750 percent) and,
simultaneously, reduces the decree of deformation (from
200,000 up to norm). values).
b. All tested materials can be divided into three croups.
(1) The first group of admixtures lowers both the deformation
degree and the solidity of vulcanized natters. This group
is comprised of emulgator E-1000 and. sapel.
(2) The second group of admixtures lowers the defo degree
but retains the tensile strength. This group is comprised
of merSolates and paraffinic acids.
(3) The third group at admixtures lowers the defo degree
at the same time increasing moderately or strongly the
solidity. This group is comprised of seral, iron-
naphtate, sodium-resinate, etc,
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CENTRAL INTELLIGENCE AGENCY
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c. It is characteristic of all three croups that they lower
the defo-degse to normal figures and considerably increase
the ductility, sometimes up to. 34,100 percent (see '
tests with benzol-sulfonic acid).
d. The use of all these admixtures usually reduces the
elasticity. eveLLadS eaeo heee-feee te eelvo
_this problem also, either by adding smaller quantities of
aluminum oxide to the rubber compound or by using special
arents for retaining the elasticity (see table 6).
10. a. This research is important because it proves aluminum
oxide to be a high quality Milne agent for rubber com-
pounds and also helped to considerably simplify production
methods and find a furnace design for aluminum oxide
production. aluminum oxide was produeed in a test cupola
furnace with exterior heating in the Luna Plant. This kind
of furnace cannot be considered a model type of an in-
dustrial furnace. eiuffle-furnaces used for aluminum oxide
production in 'aolfen and EitterfeId are also not model
furnace types if the volume of aluminum oxide and the im-
portance of this valuable filling agent for future pro-
duction is considered.
At present perfect furnace types are the modern dram rotary
furnaces with exterior and interior heating and cupola fur-
naces with interior heating. The furnaces have a high prow
duction caracity and can be 'pe rated continuously.
b. A rotary experimental furnace for aluminum oxide production
was tested in the Polysius Plant in Dessau in June 1948. The
furnace was 8 meters long and 30 to 40 cram diameter.
aluminue sulphate was introduced at one end of the drum
while the burner head was arranged at the other end. The
test showed that the whole active part escaped in the smoke
due to the great volatility of aluminum oxide. The part
of aluminum oxide which reached the onposite end of the
furnace was nonactive. This installation was not usable
as separation of a volatile material such as aluminum
oxide in gases heated to l000?C is very difficult and
reluires a very complicated plant with various systems of
cyclone filters, etc..,
c. Uupola furnaces with interior heating olariously have the
sale defects. Dr. oll proposed a noteworthy furnace con-
struction for our aluminum oxide production departnent. He
suggested the insertion of a thermax pipe of seell diameter
into a conventional rotary furnace. The heating gases cover
the outside+ of the the rmax pipe with aluminum sulphate and
aluminum oxide insides while pipe and furnace revolve.
However, such a furnace cannot be rerarded as a model type
as there is a critical shortage of thermax material. The
solidity of thermac also rapidly declines at temperatures of
1,000 to 2s000?C.
d. The tests proved normal rotary furnaces without thermax
or cupola furnaces with interior heating as the most suitable
types for the aluminum oxide production. The aluminum oxide
is seearated from the heating rases by wetting with water
or a mild soda solution or other liquids. Experiments of
this kind are presently done by Engineer Khycheyan and
Dr. ,lean.
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