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UDC 621.785.53:669.14.018.44
A combined coating for protecting turbine blades of high-temperature gas turbine engines is studied. Comparative tests of coatings under laboratory conditions and of coated blades in engine operation are performed.
The microstructure of the coating is studied and the concentration profiles of alloying elements are determined
by the method of x-ray diffraction analysis. Tests for high-temperature strength are performed.
INTRODUCTION
Coatings protecting the blades of the first turbine stage
from high-temperature oxidation have been used for over
40 year since the time when the maximum temperature on
the blades attained 850 950C. At first the blades were primarily protected by simple aluminizing performed by a powder or a slip method. Upon the creation of more powerful gas
turbine engines (GTE), the gas temperature at the inlet to the
turbine increased, which inevitably increased the maximum
temperature on the blades. For some modern engines it exceeds 1100C. This reduces considerably the rate of deterioration of the protective properties of coatings on turbine
blades and shortens their service life. The high-temperature
oxidation of the coating is accompanied by its partial removal from the most heated places due to high speeds of the
gas flow. With growth in the temperature of the blades the
strength of their material and of the material of the coating
decreases, which increases the probability of appearance of
cracks in the coating and of propagation of the cracks into
the material of the blade. In addition, growth in the temperature increases the rate of diffusion of alloying elements, primarily of nickel, from the alloy into the coating. As a result,
the content of aluminum in the coating decreases at a rate
comparable with the decrease due to oxidation and formation
of an Al2O3 film and its spalling. This circumstance was discovered by M. Fleetwood [1] when he studied the composition and structure of a coating on an aluminized nickel alloy
after 100-h hold at 1125C. Since the diffusion of nickel
from the alloy into the coating at a high temperature leads to
substantial deterioration of the protective properties, it seems
1
METHODS OF STUDY
The studies were performed on specimens and blades
fabricated from alloy ZhS32 with chemical composition of
5% Cr, 4% Re, 4% TA, 1%, Mo, 8,3% W, 1.5% Nb, 6% Al,
9% Co, 0.05% Zr, and 0.15% C [4].
In the first stage we studied specimens with a combined
double-layer coating containing a diffusion barrier. In order
to deposit a condensation coating with a thickness of about
40 mm we used a MAP-1 installation with cathode from alloy
AZh8-1 bearing Ni, Cr, Al, Ta, W, Hf, Si, and Y. Then an aluminized layer was deposited onto the specimen with the condensation coating by the method of chrome aluminizing in
vacuum at 1080C in a powder mixture containing 14% Al,
36% Cr, and 50% Al2O3. The specimen with the combined
coating was subjected to thermovacuum treatment at 1150C
for 1 h 10 min and them to annealing at 1050C.
558
0026-0673/06/1112-0558 2006 Springer Science + Business Media, Inc.
559
Cr
Al
W Ta
20
15
10
5
0
10
20
30
40
50
60
70 h, mm
most doubles. These results show that the change in the composition of the coating due to the hold at 1150C is chiefly
connected with the diffusion of nickel [6]. This agrees with
the data of [7] on diffusion processes in a NiAl Ni3Al couple at 1100C. It is shown in this work that the diffusivity of
nickel can be two orders of magnitude higher than the
diffusivity of aluminum. The curves of the distribution of alloying elements in the combined coating are presented in
Fig. 1. We should mention the high content of tungsten even
in the external zone of the coating, which promotes growth in
the strength and in the resistance of the coating to the appearance of cracks during operation of the engine.
Tests of alloy ZhS32 with various coatings for isothermal
high-temperature strength have shown that in all the coatings
the deterioration of the protective properties is accompanied
by about the same structural changes but the latter occur in
different times. For example, the coating deposited by pure
chrome aluminizing in vacuum has the following structure in
the initial state: b (NiAl) in the external zone of the coating
and b + g (Ni3Al) in the external zone. After 10 h of holding
at 1150C the external surface of the coating bears zones
with a structure of g-phase depleted of aluminum. A region
with a structure of b + g lies between these zones. In 75 h
the structure of the coating consists of a g-phase with double-phase islands of (b + g )-phases. In 100 h the structure
is considerably depleted of aluminum and the coating consists of a homogeneous g-solid solution. In 200 h the coating
is absent and the thickness of the layer depleted of aluminum
attains 30 mm.
At the beginning of the test the concentration of aluminum in the combined coating decreases markedly and that of
nickel increases. Then the rate of variation of the content of
these elements decreases noticeably. In 100 h of holding at
1150C the concentration of nickel in the coating is the same
as in the alloy, and the thickness of the coating increases.
In the initial stage of testing (20 200 h) the concentration of aluminum in the coating can be approximated by an
exponential dependence, which is typical for diffusion-controlled processes.
560
1 2 3 4
5
0
1 2 3
4
20
19
5 67
18
17
7 6 5 4 3 2 1 0
3 4
n
Fig. 2. Distribution of aluminum over the profile of a rotor blade
with combined coating (n are conventional points on the blade
profile).
When the concentration of aluminum in the coating decreases to 15 wt.%, the rate of decrease in its content grows
abruptly as a result of intense acceleration of the oxidation
due to the absence of protective film of Al2O3.
Table 1 presents the results of tests of aluminized and
combined coatings on specimens of alloy ZhS32 with about
the same content of aluminum for cyclic high-temperature
strength. It can be seen that the double-layer coating with
barrier layer bearing W and Ta is almost two times more durable than the single-layer coating. Consequently, it can be
used successfully for protecting turbine blades with maximum temperature of about 1150C on the blades.
However, for the blades to operate reliably for the entire
scheduled period it is insufficient to protect them only from
oxidation, because the main reason for rejection of a blade is
the presence of cracks in the coating and in the material of
the blade.
Coating
Content of elements
in the coating, wt.%
Al
Structure
N,*
cycles
Cr
Aluminized
17
b + g
125
Combined
18
b + g
325
The number of test cycles before exhaustion of protective properties of the coating.
Engine
tECT , h
I
II
III
88-2006
88-2124
88-2003
42
36
32
1200
400
480
Notations: n is the number of blades with combined coating; tECT is the duration of the equivalent cyclic test.
Duration
of testing, h
Cr
Ni
Co
4.0
2.0
4.5
4.0
4.25
4.95
20.0
9.0
15.3
9.9
62.5
63.9
63.9
59.5
7186
.
68.34
63.0
68.0
62.6
63.5
3.7
3.0
4.7
4.5
613
.
5.7
0.2
0.2
2.3
2.2
71
.
5.0
9.4
9.4
216
.
5.29
0
0
8.2
8.2
561
thickness of the coating in the zones of maximum temperature amounted to about 60 mm after the test. A g-phase was
located at the surface of the coating where it had the form of
a thin layer and on the interface with the alloy at about half
the thickness of the coating. Coarse inclusions of b-phase
were located between the layers of continuous g-phase. The
g-phase was also the main structural component of the coating on the trailing edges on the interface with the alloy.
Coarse grains of -phase were contained in the g-phase at
the surface of a coating with a thickness of from 20 to 50 mm.
CONCLUSIONS
1. A combined double-layer coating obtained on alloy
ZhS32 under laboratory conditions is more than twice more
durable than a standard coating with an almost equal content
of aluminum.
2. Deposition of a combined three-layer coating onto rotor blades will prolong the service life of the first-stage turbine blades to 2000 h.
REFERENCES
1. M. J. Fleetwood, J. Inst. Metals, 98, 1 7 (1970).
2. P. T. Kolomytsev, O. V. Skryl, and S. A. Kochetov, Raising the
reliability of GTE by using high-temperature coatings on the
blades, in: Structural Strength of Engines, Abs. Rep. 10th
All-Union Sci.-Eng. Conf. [in Russian], Kuibyshev (1988), p. 88.
3. V. V. Kazanov, P. T. Kolomytsev, and V. M. Samoilenko, Main
tendencies in advancement of metallic coatings for turbine
blades of gas turbine engines, in: 39th Perusal in the Memory of
K. . Tsiolkovsky, Abs. Rep. [in Russian], Kaluga (2004).
4. E. N. Kablov, I. M. Svetlov, and K. V. Petrushin, Nickel hightemperature alloys for casting blades with directed and single-crystal structure, Materialovedenie, No. 4 (1997).
5. P. T. Kolomytsev and S. A. Kochetov, A study of the mechanism
and regular features of exhaustion of protective properties of heat
resistant coatings, in: Scientific and Methodological Materials
on Protective Coatings [in Russian], VVIA Im. Zhukovskogo,
Moscow (1992), pp. 106 113.
6. P. T. Kolomytsev and S. A. Kochetov, A study of diffusion processes in a combined heat resistance coating on a high-temperature nickel alloy, in: Scientific and Methodological Materials on
Protective Coatings [in Russian], VVIA Im. Zhukovskogo, Moscow (1990), pp. 146 152.
7. M. P. Janssen, Metall. Trans., 4, 1623 1633 (1973).