[0001] The invention of this application relates to a method for producing ferritic heat-resistant
steel for use in boilers of thermal power plants, chemical industry apparatuses, and
the like that are operated at high temperatures and under low oxygen partial pressure
atmospheres.
[0002] In our country, about 60% of the total electric power demand is supplied by thermal
electric power plants using fossil fuels; however, large amount of carbon dioxide
is being emitted by the combustion of fossil fuels.
[0003] On the other hand, higher power generation efficiency is strongly demanded on thermal
power plants in view of the emission regulations on carbon dioxide for the prevention
of global warming or from the viewpoint of effective use of resource energy. Heat
resistant steel and heat resistant alloys have been used as materials resisting to
high temperatures and high pressures at thermal power plants; in the case of using
such heat resistant steel and heat resistant alloys under the atmosphere, dense oxide
coating film forms on the surface to function as protective layers.
[0004] However, in the presence of high temperature water vapor under low oxygen partial
pressure atmospheric condition as such in thermal power plant boilers, the apparatuses
used under such conditions suffer greater oxidation damage as compared with those
used under atmospheric conditions, because the supply of oxygen is not sufficient
to form protective coating films.
[0005] In general, Cr-containing heat resistant steel and heat-resistant alloys having a
Cr content of 25 mass% or more show excellent oxidation-resistance because oxidation-resistant
protective film is formed even under high temperature water vapor atmospheric condition.
[0006] Furthermore, in the case of chromium (Cr)-containing heat resistant steel and heat-resistant
alloys having a Cr content of or about 20 mass%, it is possible to modify the surface
of the base material by applying a mechanical treatment such as shot peening, or to
form an oxidation-resistant protective coating film by a method such as crystal grain
refining treatment and the like.
[0007] However, in the case of a high Cr ferritic heat-resistant steel containing 15 mass
% or less of Cr, the Cr content is too low to supply the Cr oxide necessary for forming
the oxidation-resistant protective coating film. Accordingly, as methods for ameliorating
the oxidation resistance of a high Cr ferritic heat-resistant steel containing 15
mass % or less of Cr, attempts such as increasing chromium (Cr) or silicon (Si), or
adding palladium (Pd) or platinum (Pt), etc., have been made (see, for example, literatures
1 - 4); however, they could not avoid the deterioration of the quality of material
or the increase in cost due to the addition of elements such as palladium (Pd), platinum
(Pt), etc. As described above, an effective method for improving the oxidation resistance
of a high Cr ferritic heat-resistant steel containing 15 mass % or less, for instance,
9 to 12 mass%, is yet to be realized.
Literature 1; JP-A-2002-69531
Literature 2; JP-A-2001-192730
Literature 3; JP-A-11-61342
Literature 4; JP-A-10-287960
The invention of the present application has been made under such circumstances, and
the objectives thereof are to overcome the problems of the conventional techniques
and to provide a high Cr ferritic heat-resistant steel on which an oxidation-resistant
protective coating film is formed even in the presence of high temperature water vapor
under low oxygen partial pressure atmospheric condition.
[0008] As a solution for the aforementioned problems, the invention of the application provides
the invention as follows.
[0009] The invention of the present application provides a method for producing a steel
which is a ferritic heat-resistant steel containing 7-15 mass % of Cr, in which at
least the region up to 10 µm defined by surface depth is made of a worked texture
composed of extended ferritic grains or superfine texture composed of ferrites 3 µm
or less in grain diameter, and having a Cr-rich (Cr
2O
3) protective coating film on the surface, said method characterised by applying working
at a strain rate of 0.1 sec
-1 or higher and at a working ratio of 70% or higher, in the temperature range of from
400 to 800°C to form a worked texture composed of extended ferritic grains or a superfine
texture composed of ferrites 3 µm or less in grain diameter, at least in the region
up to 10 µm defined by surface depth, and by applying pre-oxidation treatment to form
a protective coating film wherein the pre-oxidation treatment is carried out by holding
the steel for 30 to 90 minutes in the temperature range of from 400 to 800°C under
the atmosphere. It further provides a production method in which the working degree
on applying working is 0.7 or higher in true strain.
[0010] In the accompanying drawings:
Fig. 1 is a cross sectional scanning electron microscope (SEM) photograph of an intensively
worked part which have been subjected to compression working at a temperature of 500°C,
followed by pre-oxidation treatment in the atmosphere at 640°C/1h, an then by water-vapor
oxidation at 650°C/100h;
Fig. 2 is a cross sectional SEM photograph of a weakly worked part which have been
subjected to compression working at a temperature of 500°C, followed by pre-oxidation
treatment in the atmosphere at 640°C/1h, an then by water-vapor oxidation at 650°C/100h;
and
Fig. 3 is side cross sectional SEM photograph of an intensively worked part which
have been subjected to compression working at a temperature of 500°C, followed by
water-vapor oxidation at 650°C/3h without applying pre-oxidation treatment.
[0011] The invention of the application has the above characteristics, and the mode of carrying
out the invention is described below.
[0012] First of all, in ameliorating the oxidation resistance of a high Cr ferritic heat-resistant
steel containing 15 mass% or less of Cr even in the presence of high temperature water
vapor or under low oxygen partial pressure atmospheric condition, the invention of
the application is most characterized by that the oxidation resistance is improved
by applying a specific working and heat-treatment, and not by increasing the composition
of chromium (Cr) or silicon (Si), nor by adding elements such as palladium (Pd) or
platinum (Pt) and the like. Accordingly, the high Cr ferritic heat-resistant steel
obtained by the method for improving the oxidation resistance according to the invention
of the application possesses an advantage in that the physical properties and the
chemical properties of the initial composition remain without being impaired.
[0013] In general, in case the Cr content exceeds 15 mass %, as described above, the surface
layer of the steel material can be modified by applying mechanical treatment such
as shot peening and the like, or an oxidation-resistant protective coating film can
be formed by applying relatively mild crystal grain refining treatment with large
grains about 10 to 50 µm in particle diameter, however, in high Cr ferritic heat-resistant
steel containing 15 mass % or less Cr, such oxidation-resistant protective coating
film cannot be formed even if such treatment should be employed. The reason for the
above is because, in case the Cr content is 15 mass % or less, Cr necessary for forming
the protective coating film containing Cr
2O
3 as the principal component cannot be sufficiently and uniformly diffused even if
the crystal grain refining treatment for obtaining crystals about 10 to 15 µm in grain
diameters should be applied. Accordingly, oxidation-resistant protective coating film
cannot be formed in the presence of water vapor under high temperatures.
[0014] Thus, the keys of the invention of the present application are to accumulate strain
energy at high levels by applying warm intensive working to the high Cr ferritic heat-resistant
steel, or to form fine texture consisting of crystal grains 2 µm or less in grain
diameter. In the invention of the application, the reason for accumulating strain
energy at high levels or for forming fine texture consisting of crystals grains 3
µm or less in grain diameter is because, the steel material having the strain energy
accumulated in high levels easily undergoes recrystallization to form superfine grain
texture. Thus, with the formation of the superfine grain texture above, the grain
boundary area increases to contribute for the diffusion acceleration of chromium (Cr).
Then, by the uniform diffusion of chromium (Cr), chromium oxide (Cr
2O
3) is formed to function as an oxidation-resistant protective coating film. As described
above, the strain energy is highly accumulated in the invention of the application.
Further, the formation of superfine grain texture consisting of ferrite grains 3 µm
or less in grain diameter may be considered as a mode of accumulating the strain energy
at a high level.
[0015] By the thermomechanical treatment such as the rolling or the forging generally employed
in the art, it is not possible to highly accumulate the strain energy or to form a
fine texture consisting of ferritic crystal grains 3 µm or less in grain diameter
according to the invention of the present application. In order to highly accumulate
the strain energy or to form the fine crystal grain texture consisting of crystal
grains 3 µm or less in grain diameter, warm working treatment is performed at a strain
rate of 0.1 sec
-1 or higher and at a working ratio (cross section area reduction ratio) of 70 % or
higher. In case the working ratio is lower than 70 %, the accumulation of the desired
strain energy remains insufficient, and the generation of protective coating film
and the use thereof cannot be fully expected ever after the pre-oxidation treatment.
[0016] Considering the warm intense working, it is preferably carried out in the temperature
range of 400 to 800°C. Further, by forming the strain under the conditions above,
it is possible to generate the elongated ferritic grains or fine grains.
[0017] As the morphology of the elongated ferritic grains, it is preferred that it has a
shorter diameter of 5 µm or less, and most preferably, it has a shorter diameter of
3 µm or less; otherwise, the ferritic grains has a grain diameter of 3 µm or less,
and most preferably, they are fine grains 1 µm or less in grain diameter.
[0018] As described above, the invention of the present application comprises accumulating
strain energy at high levels by applying warm intensive working to the high Cr ferritic
heat-resistant steel, or forming fine texture consisting of crystal grains 3 µm or
less in grain diameter; however, the protective coating film does not always form
at high temperatures in the presence of water vapor by simply accumulating the strain
energy by warm intensive working or by forming fine crystal texture. It is necessary
to form sequentially thereafter the protective coating film by applying pre-oxidation
treatment. The pre-oxidation treatment is preferably carried out under the atmosphere
or under an inert gas (rare gas or gaseous nitrogen) atmosphere containing gaseous
oxygen, but more practical is to perform the treatment in the atmosphere. Further,
the pre-oxidation treatment is preferably performed by heat treatment in the atmosphere
at 400 - 800°C for about 30 to 90 minutes.
[0019] By combining the heat treatments above, chromium (Cr) is oxidized for the first time,
and forms Cr
2O
3 which functions as an oxidation-resistant protective coating film.
[0020] Furthermore, concerning the relation between the heating temperature of the pre-oxidation
treatment and the average crystal grain size, it is confirmed that, when heated under
the atmosphere, the grain diameter is 0.8 µm or less for the sample held at 660°C
or lower, and is 1- 2 µm for the sample held at 680 - 700°C.
[0021] As described above, the invention of the application enables forming an oxidation-resistant
protective coating film on the high Cr ferritic heat-resistant steel having a Cr content
of 7-15 mass %, on which an oxidation-resistant protective coating film had never
been formed, and this widely increases the usage of high Cr ferritic heat-resistant
steel. Furthermore, the invention of the application is advantageous in that it utilizes
heat treatment, because it does not make any changes on the composition of the high
Cr ferric heat-resistant steel. Moreover, since the protective coating film is thin
and is tightly adhered, it hardly peels off; it thereby exhibits effect on greatly
reducing the risk of causing clogging of the piping due to the peeled off scales,
or of wearing the turbine blades.
[0022] Steel, such as the high Cr ferrite heat-resistant steel specified in ASME SA335 P91
or ASME SA 213 T91, are included. These are specified in the invention of the application
by the general term "high ferritic (system)" steel.
Examples
<Example>
[0023] Mod. 9Cr-1Mo steel was subjected to 70% compression working at 500°C, and was cut
and polished in such a manner that the fine texture region and the worked texture
region should be exposed on the surface. Then, after applying pre-oxidation treatment
at 650°C for 1 h in the atmosphere, the test specimen was oxidized in water vapor
at 650°C/100 h. Fig. 1 shows the cross section SEM photograph of the intensively worked
part. The formation of the Cr-rich (Cr
2O
3) protective coating film (0.1 µm or less in thickness) on the surface was observed.
Furthermore, the crystal grain diameter of the ferritic grains in the fine texture
region under the protective coating film was found to be 1.0 µm or smaller. Further,
the shorter diameter of the elongated ferrite in the worked texture region under the
protective coating film was found to be 3 µm.
<Comparative Example1>
[0024] Mod. 9Cr-1Mo steel was subjected to pre-oxidation treatment at 680°C for 1 h in the
atmosphere, and was then subjected to water-vapor oxidation at 650°C/100 h. Fig. 2
shows the cross section SEM photograph of the resulting product, but the growth of
an Fe-rich double layer scale (about 60 µm in thickness) due to accelerated oxidation
was observed. The average grain diameter of the ferritic grains was 7 µm.
[0025] By comparing the above result with that of the Example, it was confirmed that the
high accumulation of strain energy or the formation of fine crystal texture is necessary
to form a protective coating film having resistance against water-vapor oxidation.
<Comparative Example 2>
[0026] Mod. 9Cr-1Mo steel was subjected to 70% compression working at 500°C in a manner
similar to that of Example 1, and was subjected to water-vapor oxidation at 650°C/3
h thereafter without applying pre-oxidation treatment for observation. Fig. 3 shows
the cross section SEM photograph of the intensively worked part. The formation of
double layer scale (about 10 µm in thickness) was observed.
[0027] As described in detail above, the invention of the application enables forming a
thin and highly adhesive oxidation-resistant protective coating film, which had been
believed impossible, on the high Cr ferritic steel having a Cr content of 7-15%.