Patent Application
20140311616
1. Field of the Invention
The present invention relates to a structure, and a method of manufacturing a structure.
2. Discussion of the Background
A catalytic converter is disposed in a pathway of an exhaust pipe in order to treat harmful materials contained in exhaust gases discharged from an engine.
It is necessary to keep a temperature of exhaust gases and an exhaust pipe through which the exhaust gases pass at a temperature suitable for catalyst activation (hereinafter, also referred to as a catalyst activation temperature) in order to enhance purifying efficiency of harmful materials of a catalytic converter.
In a conventional exhaust gas purifying system, a catalytic converter temperature at the time of engine start is lower than the catalyst activation temperature.
Therefore, it is required that a temperature of the exhaust pipe connected to an engine can be raised to the catalyst activation temperature in a short time from engine start.
For example, JP-A 2009-133214 discloses an exhaust pipe provided with a can-type base material made of metal and a surface coating layer comprising a crystalline inorganic material and an amorphous binder material (amorphous inorganic material), which is formed on the peripheral face of the base material.
In a conventional exhaust pipe described in JP-A 2009-133214, it is described that a heat insulating property is excellent when the thermal conductivity of the surface coating layer is lower than that of the base material. It is described that as a result of this, a temperature is likely to be raised to the catalyst activation temperature in a short time from engine start in a conventional exhaust pipe described in JP-A 2009-133214.
The contents of JP-A 2009-133214 are incorporated herein by reference in their entirety.
According to one aspect of the present invention, a structure includes a base material made of metal to be in a form of a tube and a surface coating layer provided on an inner face of the tube. The surface coating layer includes a first layer provided on the inner face and a second layer provided directly or indirectly on the first layer as an outermost layer of the surface coating layer. The first layer contains an amorphous inorganic material. The second layer contains a crystalline inorganic material having a softening point of about 950° C. or higher.
According to another aspect of the present invention, a method of manufacturing a structure includes preparing a base material made of metal to be in a form of a tube. A first layer of a surface coating layer is provided on an inner surface of the tube. The first layer contains an amorphous inorganic material. A second layer of the surface coating layer is provided directly or indirectly on the first layer as an outermost layer of the surface coating layer. The second layer contains a crystalline inorganic material having a softening point of about 950° C. or higher.
A more complete appreciation of the invention and many of the attendant advantages thereof will be readily obtained as the same becomes better understood by reference to the following detailed description when considered in connection with the accompanying drawings.
According to an embodiment of the present invention, a structure excellent in heat resistance while securing heat insulating properties, and a method for manufacturing the structure are likely to be provided. Further, the structure according to an embodiment of the present invention is particularly suitable for the case where the structure is used as an exhaust pipe.
The structure according to an embodiment of the present invention is a structure including:
a base material made of metal; and
a surface coating layer formed on the surface of the base material,
wherein
the surface coating layer includes:
a first layer which is formed on the surface of the base material and contains an amorphous inorganic material; and
a second layer which is formed as an outermost layer of the surface coating layer and contains a crystalline inorganic material having a softening point of about 950° C. or higher.
In the structure according to an embodiment of the present invention, the surface coating layer is formed on the surface of the base material made of metal. As the surface coating layer, first, the first layer containing an amorphous inorganic material is formed on the surface of the base material. The thermal conductivity of the amorphous inorganic material composing the first layer of the surface coating layer tends to be lower than that of the metal composing the base material. Accordingly, when the base material of the structure is heated, a heat transfer rate of the base material is high, but a heat transfer rate, at which heat is transferred from the base material through the surface coating layer to the outside of the structure, tends to be low.
Accordingly, particularly in a low-temperature (approximately less than about 500° C.) region in which heat conduction largely contributes to heat transfer, heat is hardly released to the outside of the structure. As a result of this, a temperature of the structure is likely to be quickly raised when the structure is heated. Thus, the structure according to an embodiment of the present invention is excellent in heat insulating properties.
Moreover, in the structure according to an embodiment of the present invention, the second layer containing a crystalline inorganic material having a softening point of about 950° C. or higher is formed as an outermost layer of the surface coating layer. Accordingly, even when the surface coating layer of the structure is exposed to a high-temperature, the crystalline inorganic material existing in the outermost layer of the surface coating layer of the structure hardly softens. Therefore, it becomes easier to prevent the surface coating layer from peeling from the base material made of metal. Thus, the structure according to an embodiment of the present invention is excellent in heat resistance.
As described above, since the structure according to an embodiment of the present invention is excellent in heat insulating properties and heat resistance, it is likely to be suitably used, for example, as an exhaust pipe.
In the structure according to the embodiment of the present invention, the crystalline inorganic material contained in the second layer of the surface coating layer is desirably one of zirconia and alumina.
Zirconia or alumina is a crystalline inorganic material having excellent heat resistance. Therefore, even when the surface coating layer of the structure is exposed to a high-temperature, zirconia or alumina existing in the outermost layer of the surface coating layer of the structure hardly softens, and therefore it becomes easier to prevent the surface coating layer from peeling from the base material made of metal.
Further, zirconia or alumina is also a crystalline inorganic material having excellent corrosion resistance. Therefore, when the surface coating layer of the structure is exposed directly to high-temperature exhaust gases, it becomes easier to prevent the surface coating layer of the structure from being corroded by at least one of nitrogen oxide (NOx) and sulfur oxide (SOx) contained in the exhaust gases. Further, if the surface coating layer of the structure is composed of only a first layer, the surface coating layer causes a problem that foreign matters adhere to the surface coating layer in softening, leading to degradation of the surface coating layer, in addition to acid corrosion, but the above problems are likely to be prevented by the second layer of the surface coating layer.
In the structure according to the embodiment of the present invention, a total thickness of the first layer and the second layer of the surface coating layer is desirably from about 1 μm to about 2000 μm.
When the total thickness of the first layer and the second layer of the surface coating layer of the structure is from about 1 μm to about 2000 μm, a heat insulating property of the structure is excellent.
When the total thickness of the first layer and the second layer of the surface coating layer of the structure is about 1 μm or more, the structure tends to ensure an adequate heat insulating property since the thickness of the surface coating layer is not too small. Further, when the total thickness of the first layer and the second layer of the surface coating layer of the structure is about 2000 μm or less, the surface coating layer is less likely to be vulnerable to a break since a degree of thermal impact to the surface coating layer hardly increases.
In the structure according to the embodiment of the present invention, the thermal conductivity at room temperature of the first layer of the surface coating layer is desirably from about 0.05 W/m·K to about 2 W/m·K.
When the thermal conductivity at room temperature of the first layer of the surface coating layer of the structure is from about 0.05 W/m·K to about 2 W/m·K, a heat transfer rate, at which heat is transferred to the outside of the structure across the surface coating layer, is likely to be slow. Consequently, the heat insulating properties of the structure are likely to be more enhanced.
It is not technically difficult that the thermal conductivity at room temperature of the first layer of the surface coating layer of the structure is brought into about 0.05 W/m·K or more. Further, when the thermal conductivity at room temperature of the first layer of the surface coating layer of the structure is about 2 W/m·K or less, the thermal conductivity of the first layer of the surface coating layer of the structure is not too large and therefore the structure tends to ensure an adequate heat insulating property.
In addition, in the present specification, the room temperature refers to 25° C.
In the structure according to the embodiment of the present invention, the first layer of the surface coating layer further desirably contains a crystalline inorganic material.
A thermal expansion coefficient of the crystalline inorganic material tends to be low, and a thermal expansion coefficient of the amorphous inorganic material tends to be high. Therefore, the thermal expansion coefficient of the first layer of the surface coating layer is likely to be controlled by adjusting a mixing ratio between the crystalline inorganic material and the amorphous inorganic material. Accordingly, by approximating the thermal expansion coefficient of the first layer of the surface coating layer to that of the base material made of a metal, adhesion between the first layer of the surface coating layer and the base material made of a metal is likely to be improved.
In the structure according to the embodiment of the present invention, the crystalline inorganic material contained in the first layer of the surface coating layer is desirably an oxide of at least one of aluminum, manganese, iron, copper, cobalt and chromium.
Since a thermal expansion coefficient of the oxide of at least one of aluminum, manganese, iron, copper, cobalt and chromium described above tends to be lower than a thermal expansion coefficient of the amorphous inorganic material, the thermal expansion coefficient of the first layer of the surface coating layer is likely to be controlled by adjusting a mixing ratio between the above-mentioned oxide and the amorphous inorganic material. Accordingly, by approximating the thermal expansion coefficient of the first layer of the surface coating layer to that of the base material made of a metal, adhesion between the first layer of the surface coating layer and the base material made of a metal is likely to be more improved.
In the structure according to the embodiment of the present invention, the base material is desirably a tubiform.
Such a structure is likely to be used as an exhaust pipe.
In addition, in the present specification, the tubiform refers to a body in which a shape of a cross section substantially perpendicular to its longitudinal direction is closed. Accordingly, in the present specification, the tubiform includes not only a body in which a shape of a cross section substantially perpendicular to its longitudinal direction is substantially round-shaped, but also bodies in which a shape of a cross section perpendicular to its longitudinal direction is substantially elliptic or substantially polygonal such as substantially rectangular. That is, specific examples of the tubiform include a substantially cylindrical body, a substantial ellipsoid and a substantially square-tube-shaped body.
In the structure according to the embodiment of the present invention, the surface coating layer is desirably formed on an inner face of the tubiform.
When the structure is used as an exhaust pipe, the surface coating layer is likely to be exposed directly to the exhaust gases. Even in such a case, in the structure, the crystalline inorganic material existing in the outermost layer of the surface coating layer hardly softens, and therefore it becomes easier to prevent the surface coating layer from peeling from the base material made of metal.
In the structure according to the embodiment of the present invention, the surface coating layer is desirably further formed on an outer face of the tubiform.
For example, by selecting the type of the crystalline inorganic material existing in the outermost layer of the surface coating layer formed on an outer face of the tubiform, the emissivity of the surface coating layer is likely to be controlled. Specifically, in the structure in which zirconia is used as the crystalline inorganic material existing in the outermost layer of the surface coating layer and stainless steel provided with an oxidized film formed on the surface is used as an metal composing the base material, the emissivity of the surface coating layer is likely to be lower than that of the base material. Thus, when the surface coating layer is further formed on an outer face of the tubiform, heat dissipation to the outside of the structure is likely to be prevented. As a result of this, the heat insulating properties of the structure in a low-temperature region is likely to be enhanced.
In the structure according to the embodiment of the present invention, the surface coating layer further desirably includes:
a third layer including inorganic fibers; and
a fourth layer containing an amorphous inorganic material,
the third layer is desirably formed on the surface of the first layer, and
the fourth layer is desirably formed between the third layer and the second layer.
The third layer of the surface coating layer is likely to have a very large porosity since it includes inorganic fibers. Accordingly, a thermal conductivity of the surface coating layer is likely to be significantly decreased. As a result of this, since a difference between the thermal conductivity of the surface coating layer and a thermal conductivity of the base material is likely to be increased, the heat insulating properties of the structure is likely to be more improved.
In the structure according to the embodiment of the present invention, the above-mentioned second layer of the surface coating layer is desirably formed by thermal spraying.
Thermal spraying is a method in which a material to be a coating is melted or softened by heating and formed into fine particles, and the fine particles are accelerated and sprayed onto the surface of an object to form a coating.
In the thermal spraying, it is thought that a coating of almost every material tends to be easily formed as long as the material is melted or softened by heating. Thus, the second layer of the surface coating layer of the structure tends to be easily formed by thermal spraying.
Further, in the structure, in which the second layer of the surface coating layer of the structure is formed by thermal spraying, the first layer of the surface coating layer of the structure is likely to mitigate thermal stress generated in the second layer (thermal-sprayed layer) of the surface coating layer of the structure in an environment in which thermal impact such as rapid temperature rise or rapid temperature drop is added to the structure. The reason for this is likely that if the second layer of the surface coating layer, having heat resistance, is formed by thermal spraying, high-temperature and high-speed particles to become a thermal-sprayed layer impinge on the first layer of the surface coating layer containing an amorphous inorganic material, and the particles to become a thermal-sprayed layer are engaged in the first layer of the surface coating layer, and consequently the second layer of the surface coating layer is likely to firmly adhere to the first layer of the surface coating layer of the structure. Accordingly, in the structure, peeling of the surface coating layer due to thermal impact is likely to be prevented.
The method for manufacturing a structure according to the embodiment of the present invention, including processes of:
preparing a base material made of metal; and
forming a surface coating layer on the surface of the base material,
wherein
the process of forming the surface coating layer includes:
a process of forming a first layer of the surface coating layer, containing an amorphous inorganic material, on the surface of the base material; and
a process of forming a second layer of the surface coating layer, containing a crystalline inorganic material having a softening point of about 950° C. or higher, as an outermost layer of the surface coating layer.
In the method for manufacturing the structure according to the embodiment of the present invention, a structure excellent in heat resistance while securing heat insulating properties is likely to be manufactured, as described in the structure according to the embodiments of the present invention.
In the method for manufacturing the structure according to the embodiment of the present invention, the above-mentioned process of forming the surface coating layer further desirably includes:
a process of forming a third layer of the surface coating layer, including inorganic fibers, on the surface of the first layer of the surface coating layer; and
a process of forming a fourth layer of the surface coating layer, containing an amorphous inorganic material, between the third layer of the surface coating layer and the second layer of the surface coating layer.
In the above method for manufacturing the structure, a structure having more excellent heat insulating properties is likely to be manufactured since the structure including a surface coating layer further including a third layer including inorganic fibers and a fourth layer containing an amorphous inorganic material is likely to be manufactured.
In the method for manufacturing the structure according to the embodiment of the present invention, the second layer of the surface coating layer is desirably formed by thermal spraying.
In the above method for manufacturing the structure, as described above, the second layer of the surface coating layer of the structure tends to be easily formed by thermal spraying.
Further, if the second layer of the surface coating layer, having heat resistance, is formed by thermal spraying, high-temperature and high-speed particles to become a thermal-sprayed layer impinge on the first layer of the surface coating layer containing an amorphous inorganic material, and the particles to become a thermal-sprayed layer are engaged in the first layer of the surface coating layer, and consequently the second layer of the surface coating layer is likely to firmly adhere to the first layer of the surface coating layer of the structure. Accordingly, the first layer of the surface coating layer of the structure is likely to mitigate thermal stress generated in the second layer (thermal-sprayed layer) of the surface coating layer of the structure in an environment in which thermal impact such as rapid temperature rise or rapid temperature drop is added to the structure, and as a result of this, peeling of the surface coating layer due to thermal impact is likely to be prevented.
Hereinafter, the embodiments will now be described with reference to the accompanying drawings, wherein like reference numerals designate corresponding or identical elements throughout the various drawings. However, the present invention is not limited to the following embodiments, and variations may be appropriately made without departing from the gist of the present invention.
Hereinafter, a first embodiment, which is an embodiment of the structure and the method for manufacturing a structure of the present invention, will be described.
First, a structure of the first embodiment of the present invention will be described.
The structure 1A shown in
In the structure 1A shown in
The surface coating layer 20a of the structure 1A of the first embodiment of the present invention has a two-layer structure, and specifically, it has a structure in which two layers of the first layer 21a and the second layer 22a are laminated in this order from the side of the base material 10a. In other words, the first layer 21a of the surface coating layer 20a is formed on the surface of the base material 10a, and the second layer 22a of the surface coating layer 20a is formed on the surface of the first layer 21a of the surface coating layer 20a and formed as an outermost layer of the surface coating layer 20a.
Examples of a material of the base material of the structure include metals such as stainless steel, steel, iron and copper; and nickel alloys such as inconel, hastelloy and invar. With respect to these metal materials of the base material, as described later, by approximating their thermal expansion coefficients to the thermal expansion coefficient of a material composing the first layer of the surface coating layer, adhesion between the first layer of the surface coating layer and the base material made of a metal is likely to be improved.
A shape of the base material is not particularly limited, but when the base material is used for an exhaust pipe, a tubiform is preferred, and a substantially cylindrical shape is more preferred.
The amorphous inorganic material contained in the first layer of the surface coating layer of the structure is preferably a low melting point glass having a softening point of from about 300° C. to about 1000° C. Further, a type of the low melting point glass is not particularly limited, and examples thereof include soda-lime glass, alkali-free glass, borosilicate glass, kali glass (potash glass), crystal glass, titanium crystal glass, barium glass, boron glass, strontium glass, alumina-silicate glass, soda-zinc glass and soda-barium glass.
These glasses may be used singly or may be used as a mixture of two or more of them.
If the low melting point glass as described above has a softening point in the range of from about 300° C. to about 1000° C., the first layer of the surface coating layer tends to be easily and firmly formed on the surface of the base material made of a metal material by melting the low melting point glass, applying (coating) it onto the surface of the base material (metal material), and then firing by heating.
When the softening point of the low melting point glass is about 300° C. or higher, the low melting point glass is hardly softened when using it as an exhaust pipe to hardly cause an extraneous material to adhere to the surface coating layer of the structure. On the other hand, when the softening point of the low melting point glass is about 1000° C. or lower, the base material hardly degrades due to heat treatment in forming the surface coating layer of the structure.
In addition, the softening point can be measured according to the method specified in JIS R 3103-1 (2001) using, for example, Automatic Measuring Apparatus of Glass Softening and Strain Points (SSPM-31) manufactured by OPT Corporation.
The contents of JIS R 3103-1 (2001) are incorporated herein by reference in their entirety.
A type of the borosilicate glass is not particularly limited, and examples thereof include SiO2—B2O3—ZnO glass and SiO2—B2O3—Bi2O3 glass. The crystal glass refers to glasses containing PbO, and its type is not particularly limited, and examples of the crystal glasses include SiO2—PbO glass, SiO2—PbO—B2O3 glass, and SiO2—B2O3—PbO glass. A type of the boron glass is not particularly limited, and examples thereof include B2O3—ZnO—PbO glass, B2O3—ZnO—Bi2O3 glass, B2O3—Bi2O3 glass, and B2O3—ZnO glass. A type of the barium glass is not particularly limited, and examples thereof include BaO—SiO2 glass.
Further, the amorphous inorganic material may include only one low melting point glass or may include a plurality of low melting point glasses among low melting point glasses described above.
A crystalline inorganic material contained in the second layer of the surface coating layer of the structure has a higher softening point than that of the amorphous inorganic material contained in the first layer of the surface coating layer of the structure. Specifically, the crystalline inorganic material contained in the second layer of the surface coating layer of the structure has a softening point of about 950° C. or higher.
Specific examples of the crystalline inorganic material contained in the second layer of the surface coating layer of the structure include zirconia and alumina.
More specific examples of composition of zirconia include CaO stabilized zirconia (about 5 wt % CaO—ZrO2, about 8 wt % CaO—ZrO2, about 31 wt % CaO—ZrO2), MgO stabilized zirconia (about 20 wt % MgO—ZrO2, about 24 wt % MgO—ZrO2), Y2O3 stabilize zirconia (about 6 wt % Y2O3—ZrO2, about 7 wt % Y2O3—ZrO2, about 8 wt % Y2O3—ZrO2, about 10 wt % Y2O3—ZrO2, about 12 wt % Y2O3—ZrO2, about 20 wt % Y2O3—ZrO2), zircon (ZrO2— about 33 wt % SiO2), and CeO stabilized zirconia. Further, more specific examples of composition of alumina include white alumina (Al2O3), gray alumina (Al2O3— about 1.5 to about 4 wt % TiO2), alumina.titania (Al2O3— about 13 wt % TiO2, Al2O3— about 20 wt % TiO2, Al2O3— about 40 wt % TiO2, Al2O3— about 50 wt % TiO2), alumina.yttria (3Al2O3.5Y2O3), alumina.magnesia (Mg.Al2O4), and alumina.silica (3Al2O3.2SiO2).
Among these, zirconia having a low thermal conductivity, which is superior in heat resistance and corrosion resistance and has a thermal conductivity of about 4 W/mK or less at 25° C., is preferred, and Y2O3 stabilized zirconia is more preferred.
The structure 1B shown in
The structure 1B shown in
In the structure 1B shown in
As with the structure 1A shown in
The structure 10 shown in
In the structure 10 shown in
As with the structure 1A shown in
The structure 1D shown in
In the structure 1D shown in
As with the structure 1A shown in
When a crystalline inorganic material is contained in the first layer of the surface coating layer of the structure like the structure 1B shown in
The inorganic particles composed of these oxides may be used singly or may be used as a mixture of two or more of them.
Among the materials composing the first layer of the surface coating layer of the structure, the thermal expansion coefficient of the crystalline inorganic material including an oxide of a transition metal tends to be as low as from about 8×10−6/° C. to about 9×10−6/° C., and the thermal expansion coefficient of the amorphous inorganic material including a low melting point glass tends to be as high as from about 8×10−6/° C. to about 25×10−6/° C. Therefore, the thermal expansion coefficient of the first layer of the surface coating layer of the structure is likely to be controlled by adjusting a mixing ratio between the crystalline inorganic material and the amorphous inorganic material. On the other hand, among the materials composing the base material, a thermal expansion coefficient of stainless steel is from about 10×10−6/° C. to about 18×10−6/° C. Accordingly, by adjusting a mixing ratio between the crystalline inorganic material and the amorphous inorganic material, the thermal expansion coefficient of the first layer of the surface coating layer of the structure is likely to be approximated to that of the base material. As a result, adhesion between the first layer of the surface coating layer of the structure and the base material is likely to be improved.
A difference between the thermal expansion coefficient of the first layer of the surface coating layer of the structure and the thermal expansion coefficient of the base material is desirably about 10×10−6/° C. or less. When the difference between both is about 10×10−6/° C. or less, since adhesion between both is likely to be strong, peeling of one from the other or deformation or failure of the surface coating layer of the structure and the base material particularly hardly occurs even though the surface coating layer of the structure is exposed to a high-temperature.
When pores exist in the first layer of the surface coating layer of the structure like the structure 10 shown in
When pores are present in the first layer of the surface coating layer of the structure, the porosity of the first layer of the surface coating layer of the structure is desirably from about 5% to about 90%, and more desirably from about 10% to about 70%.
When the porosity of the first layer of the surface coating layer of the structure is about 5% or more, the adequate effect of improving the heat insulating properties of the structure tends to be achieved since the percentage of the pores contributing to a reduction in thermal conductivity is not too small. On the other hand, when the porosity of the first layer of the surface coating layer of the structure is about 90% or less, since the percentage of the pores is not too large, strength of the first layer of the surface coating layer of the structure is hardly deteriorated. As a result of this, it becomes easier to adequately ensure the strength of the structure. Moreover, when the porosity of the first layer of the surface coating layer of the structure is about 90% or less, since the percentage of the pores is not too large, it becomes easier to ensure the adhesion of the first layer of the surface coating layer of the structure to the base material.
The porosity of the first layer of the surface coating layer of the structure can be measured by the following method. First, an orthogonal cross section of the structure is observed with a scanning electron microscope (SEM), and a photograph of a SEM image is taken. Next, the SEM image is imported in a personal computer, and the SEM image is converted to a binary image (pore area and non-pore area) using an image analysis software (for example, Photoshop manufactured by Adobe Systems Inc.). An area of a pore area existing in the first layer of the surface coating layer is measured. Then, a ratio of the area of the pore area to a total area of the pore area and the first layer of the surface coating layer is calculated and this calculated value is taken as a porosity of the first layer of the surface coating layer.
In addition, the orthogonal cross section of the structure refers to a cross section of the structure substantially orthogonal to a plane in which the surface coating layer is formed.
Further, the porosity of the first layer of the surface coating layer can also be determined by actually measuring a thickness and a weight of the first layer of the surface coating layer to determine a bulk density of the first layer of the surface coating layer, and calculating a ratio of the bulk density to a true density of the first layer of the surface coating layer.
The structure 1E shown in
In the structure 1E shown in
The surface coating layer 20a of the structure 1E is formed on the surface on a smaller area side of the surfaces of the base material 10b.
A configuration of the surface coating layer 20a in the structure 1E is similar to that of the surface coating layer 20a in the structure 1A shown in
In addition, in the structure of the first embodiment of the present invention, when a substantially semicylindrical-shaped base material is used, a face, on which the surface coating layer is formed, may be a surface on a larger area side (surface opposite to the form shown in
In the structure of the first embodiment of the present invention, the surface coating layer may be formed on both faces of the substantially semicylindrical-shaped base material.
In the structure 1F shown in
The surface coating layer 20a of the structure 1F is formed on the surface (inner face) on a smaller area side of the surfaces of the base material 10c.
A configuration of the surface coating layer 20a in the structure 1F is similar to that of the surface coating layer 20a in the structure 1A shown in
In addition, in the structure of the first embodiment of the present invention, when a substantially cylindrical-shaped base material is used, a face, on which the surface coating layer is formed, may be a surface (outer face) on a larger area side.
In the structure 1G shown in
The surface coating layer 20a of the structure 1G is formed on both faces, namely an inner face and an outer face, of the base material 10c.
A configuration of the surface coating layer 20a in the structure 1G is similar to that of the surface coating layer 20a in the structure 1A shown in
In addition, in the structure of the first embodiment of the present invention, when a substantially semicylindrical-shaped base material or a substantially cylindrical-shaped base material is used, on the surface of the base material, any of the surface coating layer 20b in the structure 1B shown in
In the structure of the first embodiment of the present invention, the total thickness of the first layer and the second layer of the surface coating layer in the structure is desirably from about 1 μm to about 2000 μm, and more desirably from about 25 μm to about 750 μm.
When the total thickness of the first layer and the second layer of the surface coating layer of the structure is about 1 μm or more, the structure tends to ensure an adequate heat insulating property since the thickness of the surface coating layer of the structure is not too small. Further, when the total thickness of the first layer and the second layer of the surface coating layer of the structure is about 2000 μm or less, the surface coating layer is less likely to be vulnerable to a break since a degree of thermal impact to the surface coating layer of the structure hardly increases.
In the structure of the first embodiment of the present invention, the thickness of the first layer of the surface coating layer in the structure is desirably from about 0.5 μm to about 1200 μm, and more desirably from about 15 μm to about 500 μm.
When the thickness of the first layer of the surface coating layer of the structure is about 0.5 μm or more, the structure tends to ensure an adequate heat insulating property since the percentage of the amorphous inorganic material in the structure is not too small. Further, when the thickness of the first layer of the surface coating layer of the structure is about 1200 μm or less, in the case of forming a surface coating layer having a predetermined thickness, the thickness of the second layer of the surface coating layer hardly becomes small and therefore the structure tends to ensure an adequate heat resistance.
In the structure of the first embodiment of the present invention, the thickness of the second layer of the surface coating layer of the structure is desirably from about 0.5 μm to about 800 μm, and more desirably from about 10 μm to about 250 μm.
When the thickness of the second layer of the surface coating layer of the structure is about 0.5 μm or more, the structure tends to ensure an adequate heat resistance since the percentage of the crystalline inorganic material existing in the outermost layer of the surface coating layer of the structure is not too small. Further, when the thickness of the second layer of the surface coating layer of the structure is about 800 μm or less, in the case of forming a surface coating layer having a predetermined thickness, the thickness of the first layer of the surface coating layer of the structure hardly becomes small and therefore the structure tends to ensure an adequate heat insulating property.
In the structure of the first embodiment of the present invention, the thermal conductivity at room temperature (25° C.) of the first layer of the surface coating layer of the structure is desirably from about 0.05 W/m·K to about 2 W/m·K, and more desirably from about 0.1 W/m·K to about 2 W/m·K.
It is not technically difficult that the thermal conductivity at room temperature of the first layer of the surface coating layer of the structure is brought into about 0.05 W/m·K or more. Further, when the thermal conductivity at room temperature of the first layer of the surface coating layer of the structure is about 2 W/m·K or less, the thermal conductivity of the first layer of the surface coating layer of the structure is not too large and therefore the structure tends to ensure an adequate heat insulating property.
The thermal conductivity at a room temperature of the first layer of the surface coating layer of the structure can be measured by a laser flash method.
Next, a method for manufacturing a structure of the first embodiment of the present invention will be described.
The method for manufacturing a structure of the first embodiment of the present invention is a method for manufacturing a structure including a base material made of metal and a surface coating layer formed on the surface of the base material, the method including processes of:
preparing a base material made of metal; and
forming a surface coating layer on the surface of the base material,
wherein
the process of forming the surface coating layer includes:
a process of forming a first layer of the surface coating layer, containing an amorphous inorganic material, on the surface of the base material; and
a process of forming a second layer of the surface coating layer, containing a crystalline inorganic material having a softening point of about 950° C. or higher, as an outermost layer of the surface coating layer.
Specifically, in the process of forming the surface coating layer, the first layer of the surface coating layer is formed on the surface of the base material, and then the second layer of the surface coating layer is formed on the surface of the first layer of the surface coating layer.
Here, taking the case where the structure 1B shown in
(1) Process of Preparing Base Material Made of Metal
Starting from a base material made of metal (hereinafter, referred to as a metal base material or metal material), first, a cleaning process is performed in order to remove impurities on the surface of the metal base material.
The cleaning process is not particularly limited and publicly known cleaning process can be employed, and specifically, a process in which ultrasonic cleaning is carried out in an alcohol solvent can be employed.
Further, after the cleaning process, as required, the surface of the metal base material may be subjected to a roughening process in order to increase a specific surface area of the surface of the metal base material or to adjust the surface roughness of the metal base material. Specifically, for example, roughening processes such as sand blasting, etching, and high temperature oxidation may be performed. These processes may be used singly or in combination of two or more of them.
After the roughening process, a cleaning process may be further carried out.
(2) Process of Forming First Layer of Surface Coating Layer
First, the crystalline inorganic material and amorphous inorganic material are mixed to prepare a raw material composition for the first layer of the surface coating layer.
Specifically, for example, a powder of the crystalline inorganic material and a powder of the amorphous inorganic material are adjusted so as to have a predetermined particle size and particle shape, and the respective powders are dry-mixed at a predetermined rate to prepare a mixed powder. Water is added to the mixed powder, and the resulting mixture is wet-mixed with a ball mill to prepare a raw material composition for the first layer of the surface coating layer.
Here, a mixing ratio of the mixed powder to water is not particularly limited, but it is desired that the amount of water is about 100 parts by weight with respect to 100 parts by weight of the mixed powder. The reason for this is that this mixing ratio yields viscosity suitable for application to the metal base material. Further, as required, the dispersion medium such as an organic solvent and the organic binder may be added to the raw material composition for the first layer of the surface coating layer.
Next, the surface of the metal base material is coated with the raw material composition for the first layer of the surface coating layer.
As a method of coating the base material with the raw material composition for the first layer of the surface coating layer, a method such as spray coating, electrostatic coating, ink-jet, transfer using a stamp or a roll, brush painting and electrode position coating may be used.
Or, the metal base material may be coated with the raw material composition for the first layer of the surface coating layer by immersing the metal base material in the raw material composition for the first layer of the surface coating layer.
Subsequently, the metal base material coated with the raw material composition for the first layer of the surface coating layer is subjected to firing process.
Specifically, the metal base material coated with the raw material composition for the first layer of the surface coating layer is dried, and then fired by heating to form a first layer of the surface coating layer.
A temperature of the firing is desirably a softening point of the amorphous inorganic material or more, and desirably from about 700° C. to about 1100° C., varying depending on the type of the amorphous inorganic material mixed. When the firing temperature is set at a temperature of a softening point of the amorphous inorganic material or more, the amorphous inorganic material is likely to firmly adhere to the metal base material, and the first layer of the surface coating layer firmly adhering to the metal base material is likely to be formed.
(3) Process of Forming Second Layer of Surface Coating Layer
The second layer of the surface coating layer, containing a crystalline inorganic material having a softening point of about 950° C. or higher, is formed on the surface of the first layer of the surface coating layer which has been formed in the above process (2).
In the method for manufacturing a structure of the first embodiment of the present invention, the second layer of the surface coating layer is formed by a thermal spraying method since by this method, formation of a layer is easy and adhesion between the first layer and the second layer of the surface coating layer is excellent. However, the second layer of the surface coating layer may be formed, for example, by an electron beam physical vapor deposition method other than the thermal spraying method.
As the thermal spraying method, a method of plasma spraying, flame spraying, high speed flame spraying, vacuum spraying, arc spraying, wire spraying or explosion spraying can be employed. Among these, plasma spraying which is likely to form a coating excellent in heat resistance is preferred, and gas plasma spraying is more preferred.
In the methods using gas plasma spraying, the second layer of the surface coating layer is formed on the surface of the metal base material with the first layer of the surface coating layer formed on the metal base material by thermal-spraying a powder of the crystalline inorganic material composing the second layer of the surface coating layer by use of gas plasma of Ar—H2 or the like.
When the second layer of the surface coating layer is formed by using gas plasma spraying, spraying conditions such as a spraying current, a spraying voltage, a spraying distance, a powder-supply rate, amounts of Ar/H2 are appropriately selected in accordance with a temperature of the sprayed particle (particle of the melted or softened crystalline inorganic material) and a desired thickness of the second layer of the surface coating layer.
Further, when the second layer of the surface coating layer is formed by using gas plasma spraying, a temperature at the time when the sprayed particles adhere to the surface of the first layer of the surface coating layer is maintained at a softening point of the amorphous inorganic material composing the first layer of the surface coating layer, or more. Thereby, the high-temperature and high-speed sprayed particles to become a thermal-sprayed layer (second layer of the surface coating layer) impinge on the first layer, containing an amorphous inorganic material, of the surface coating layer, and the sprayed particles to become a thermal-sprayed layer are engaged in the first layer of the surface coating layer, and consequently the second layer of the surface coating layer is likely to firmly adhere to the first layer of the surface coating layer of the structure.
In addition, when the second layer of the surface coating layer is formed, it is more preferred to perform the thermal spraying with the amorphous inorganic material (glass, etc.) composing the first layer of the surface coating layer softened by heating the metal base material with the first layer of the surface coating layer formed on its surface. The reason for this is that by performing thermal spraying with the amorphous inorganic material composing the first layer of the surface coating layer softened, the sprayed particles to become a thermal-sprayed layer are more engaged in the first layer of the surface coating layer, and consequently the second layer of the surface coating layer is likely to firmly adhere to the first layer of the surface coating layer of the structure.
By the above procedure, a structure 1B, which is an example of the structure of the first embodiment of the present invention and is shown in
In addition, when the structure 1A shown in
Further, when the structure 10 shown in
Among these, the pore-forming agent is preferably used.
As the pore-forming agent, for example, balloons which are fine hollow spheres composed of oxide base ceramic, spheric acrylic particles, and graphite can be used.
Further, an example of a method for manufacturing the structure, in which a base material is a tubiform and a surface coating layer is formed on the inner face of the tubiform like a structure 1F shown in
First, as the metal base material, a first half-cut member and a second half-cut member obtained by cutting a tubiform in substantially half are prepared. Next, the surface on a smaller area side of each of the first half-cut member and the second half-cut member is coated with the raw material composition for the first layer of the surface coating layer. Subsequently, the first half-cut member and the second half-cut member are subjected to a firing process to form a first layer of the surface coating layer on the surface of the first half-cut member and the second half-cut member, respectively. Then, with respect to the first half-cut member and the second half-cut member, a second layer of the surface coating layer, containing a crystalline inorganic material having a softening point of about 950° C. or higher, is formed on the surface of the first layer of the surface coating layer by using a method such as thermal spraying. Thereafter, the first half-cut member is joined to the second half-cut member by welding etc. to form a tubiform.
By the above procedure, a structure, in which the metal base material is a tubiform and the surface coating layer is formed on an inner face of the tubiform, can be manufactured.
Moreover, when as with the structure 1G shown in
Hereinafter, the effects of the structure and the method for manufacturing the structure of the first embodiment of the present invention will be enumerated.
(1) In the structure of the present embodiment, the surface coating layer is formed on the surface of the base material made of metal. As the surface coating layer, first, the first layer containing an amorphous inorganic material is formed on the surface of the base material. The thermal conductivity of the amorphous inorganic material composing the first layer of the surface coating layer tends to be lower than that of the metal composing the base material. Accordingly, when the base material of the structure is heated, a heat transfer rate of the base material is high, but a heat transfer rate, at which heat is transferred from the base material through the surface coating layer to the outside of the structure, tends to be low.
Accordingly, particularly in a low-temperature (approximately less than about 500° C.) region in which heat conduction largely contributes to heat transfer, heat is hardly released to the outside of the structure. As a result of this, a temperature of the structure is likely to be quickly raised when the structure is heated. Thus, the structure in the present embodiment is excellent in heat insulating properties.
(2) In the structure in the present embodiment, as the surface coating layer, the second layer containing a crystalline inorganic material (crystalline inorganic material having a softening point of about 950° C. or higher) having a higher softening point than that of the amorphous inorganic material composing the first layer is formed as an outermost layer of the surface coating layer. Accordingly, even when the surface coating layer of the structure is exposed to a high-temperature, the crystalline inorganic material existing in the outermost layer of the surface coating layer of the structure hardly softens. Therefore, it becomes easier to prevent the surface coating layer from peeling from the base material made of metal. Thus, the structure in the present embodiment is excellent in heat resistance.
As described above, since the structure in the present embodiment is excellent in heat insulating properties and heat resistance, it is likely to be suitably used, for example, as an exhaust pipe.
(3) In the structure in the present embodiment, the crystalline inorganic material contained in the second layer of the surface coating layer is zirconia or alumina.
Zirconia or alumina is a crystalline inorganic material having excellent heat resistance. Therefore, even when the surface coating layer of the structure is exposed to a high-temperature, zirconia or alumina existing in the outermost layer of the surface coating layer of the structure hardly softens, and therefore it becomes easier to prevent the surface coating layer from peeling from the base material made of metal.
Further, zirconia or alumina is also a crystalline inorganic material having excellent corrosion resistance. Therefore, when the surface coating layer of the structure is exposed directly to high-temperature exhaust gases, it becomes easier to prevent the surface coating layer of the structure from being corroded by at least one of nitrogen oxide (NOx) and sulfur oxide (SOx) contained in the exhaust gases. Further, if the surface coating layer of the structure is composed of only a first layer, the surface coating layer causes a problem that foreign matters adhere to the surface coating layer in softening, leading to degradation of the surface coating layer, in addition to acid corrosion, but the above problems are likely to be prevented by the second layer of the surface coating layer.
(4) In the structure in the present embodiment, the total thickness of the first layer and the second layer of the surface coating layer is from about 1 μm to about 2000 μm.
When the total thickness of the first layer and the second layer of the surface coating layer of the structure is from about 1 μm to about 2000 μm, a heat insulating property of the structure is excellent.
(5) In the structure in the present embodiment, the thermal conductivity at room temperature of the first layer of the surface coating layer is from about 0.05 W/m·K to about 2 W/m·K.
When the thermal conductivity at room temperature of the first layer of the surface coating layer of the structure is from about 0.05 W/m·K to about 2 W/m·K, a heat transfer rate, at which heat is transferred to the outside of the structure across the surface coating layer, is likely to be low. Consequently, the heat insulating properties of the structure is likely to be more enhanced.
(6) In the method for manufacturing the structure in the present embodiment, the above-mentioned second layer of the surface coating layer is formed by thermal spraying.
In the thermal spraying, it is thought that a coating of almost every material tends to be easily formed as long as the material is melted or softened by heating. Thus, the second layer of the surface coating layer of the structure tends to be easily formed by thermal spraying.
Further, if the second layer of the surface coating layer, having heat resistance, is formed by thermal spraying, high-temperature and high-speed particles to become a thermal-sprayed layer impinge on the first layer coating layer, containing an amorphous inorganic material, of the surface, and the particles to become a thermal-sprayed layer are engaged in the first layer of the surface coating layer, and consequently the second layer of the surface coating layer is likely to firmly adhere to the first layer of the surface coating layer of the structure. Accordingly, the first layer of the surface coating layer of the structure is likely to mitigate thermal stress generated in the second layer (thermal-sprayed layer) of the surface coating layer of the structure in an environment in which thermal impact such as rapid temperature rise or rapid temperature drop is added to the structure, and as a result of this, peeling of the surface coating layer due to thermal impact is likely to be prevented.
Hereinafter, examples in which the first embodiment of the present invention is more specifically disclosed will be described. In addition, the present invention is not limited to only these examples.
A flat plate stainless steel base material (SUS430) having a size of 40 mm in length, 40 mm in width and 1.5 mm in thickness was used as a base material made of metal, and the base material was subjected to ultrasonic cleaning in an alcohol solvent, and subsequently sand blasted to roughen the surface (both sides) of the base material. Sand blasting was carried out for 10 minutes using #100 Al2O3 abrasive grain.
The surface roughness of the metal base material was measured by use of a surface roughness measuring apparatus (HANDY SURF E-35B manufactured by Tokyo Seimitsu Co., Ltd.), and consequently the surface roughness of the metal base material was RzJIS=8.8 μm.
By the above processing, a flat plate base material was prepared.
As a powder of the amorphous inorganic material, K4006A-100M (Bi2O3—B2O3 glass, softening point 770° C.) manufactured by Asahi Glass Co., Ltd. was prepared.
As an organic binder, methylcellulose (trade name: METOLOSE-65SH) manufactured by Shin-Etsu Chemical Co., Ltd. was prepared.
In preparation of the raw material composition for the first layer of the surface coating layer, 100 parts by weight of water was further added to 100 parts by weight of powder of the amorphous inorganic material, and the resulting mixture was wet-mixed with a ball mill to prepare slurry.
In addition, in preparation of the raw material composition for the first layer of the surface coating layer, from 0.1 wt % to 3 wt % of the organic binder was added, taking a total weight of the raw material composition for the first layer as 100 wt %. Furthermore, 10 parts by weight of fine hollow spheres predominantly composed of silica was added as a pore-forming agent.
The raw material composition for the first layer of the surface coating layer was applied onto one surface of a flat base material by spray coating, and dried at 70° C. for 20 minutes in a drying apparatus. Subsequently, this was fired by heating at 850° C. for 15 minutes in the air to form a first layer of the surface coating layer having a thickness of 200 μm.
Subsequently, a second layer, having a thickness of 200 μm, of the surface coating layer was formed by thermal-spraying a powder of 8 wt % Y2O3 stabilized ZrO2 (manufactured by Sulzer Metco Ltd., Metco 204NS-G) which is a crystalline inorganic material onto the surface of the above-mentioned first layer of the surface coating layer.
As a thermal spraying apparatus, a plasma flame spraying apparatus (manufactured by Sulzer Metco (Japan) Ltd., 7MC) was employed. Spraying conditions are as follows; spraying current: 500 A, spraying voltage: 75 V, spraying distance: 75 mm, powder-supply rate: 25 g/min, amounts of Ar/H2: 70 l/min/10 l/min. Thereby, a temperature at the time when the sprayed particles adhere to the surface of the first layer of the surface coating layer was set at 800° C. or more.
By the above procedure, a structure in Example 1 was manufactured.
The total thickness of the first layer and the second layer of the surface coating layer in the structure in Example 1 is 400 μm.
A first layer of the surface coating layer was formed in the approximately same manner as in Example 1. However, a thickness of the first layer of the surface coating layer was adjusted to 300 μm by changing the amount of the raw material composition for the first layer of the surface coating layer to be applied. Further, when the first layer of the surface coating layer was formed, a raw material composition for the first layer of the surface coating layer, in which a mixing amount of fine hollow spheres was changed from 10 parts by weight to 20 parts by weight to change the porosity of the surface coating layer, was applied, and then fired by heating.
Subsequently, a second layer of the surface coating layer, having a thickness of 200 μm, was formed in the approximately same manner as in Example 1.
By the above procedure, a structure in Example 2 was manufactured.
The total thickness of the first layer and the second layer of the surface coating layer in the structure in Example 2 is 500 μm.
Using the raw material composition for the first layer of the surface coating layer used in Example 1, a first layer of the surface coating layer was formed in the approximately same manner as in Example 1. However, a thickness of the first layer of the surface coating layer was adjusted to 500 μm by changing the application amount of the raw material composition for the first layer of the surface coating layer.
Subsequently, a second layer of the surface coating layer was formed in the approximately same manner as in Example 1. However, the thickness of the second layer of the surface coating layer was adjusted to 300 μm by changing a thermal spraying time.
By the above procedure, a structure in Example 3 was manufactured.
The total thickness of the first layer and the second layer of the surface coating layer in the structure in Example 3 is 800 μm.
Using the raw material composition for the first layer of the surface coating layer used in Example 2, a first layer of the surface coating layer was formed in the approximately same manner as in Example 1. However, a thickness of the first layer of the surface coating layer was adjusted to 1000 μm by changing the application amount of the raw material composition for the first layer of the surface coating layer.
Subsequently, a second layer of the surface coating layer, having a thickness of 200 μm, was formed in the approximately same manner as in Example 1.
By the above procedure, a structure in Example 4 was manufactured.
The total thickness of the first layer and the second layer of the surface coating layer in the structure in Example 4 is 1200 μm.
A powder of a CoNiCrAlY alloy (Co-32 wt % Ni-21 wt % Cr-8 wt % Al-0.5% Y) was prepared as a metal powder of a material for forming the first layer of the surface coating layer.
Next, the powder of a CoNiCrAlY alloy was thermal-sprayed onto one surface of a plate-like base material under the same spraying condition as in Example 1 to form a first layer of the surface coating layer having a thickness of 200 μm.
Subsequently, a second layer of the surface coating layer was formed in the approximately same manner as in Example 1. However, the thickness of the second layer of the surface coating layer was adjusted to 300 μm by changing a thermal spraying time.
By the above procedure, a structure in Comparative Example 1 was manufactured.
The total thickness of the first layer and the second layer of the surface coating layer in the structure in Comparative Example 1 is 500 μm.
A first layer of the surface coating layer was formed in the approximately same manner as in Example 1. However, a thickness of the first layer of the surface coating layer was adjusted to 500 μm by changing the application amount of the raw material composition for the first layer of the surface coating layer. Further, a pore-forming agent was not added in preparation of the raw material composition for the first layer of the surface coating layer.
In Comparative Example 2, the second layer of the surface coating layer was not formed.
By the above procedure, a structure in Comparative Example 2 was manufactured.
The total thickness of the first layer and the second layer of the surface coating layer in the structure in Comparative Example 2 is 500 μm.
Configurations (types and thicknesses of the first layer and the second layer of the surface coating layer) of the surface coating layer of the structures in Examples 1 to 4 and Comparative Examples 1 and 2 are collectively shown in Table 1.
Further, characteristics (thermal conductivity and porosity of the first layer of the surface coating layer, heat resistance, thermal impact resistance and corrosion resistance) of the structures in Examples 1 to 4 and Comparative Examples 1 and 2 were evaluated by the following procedure, and the results of evaluation of the characteristics were collectively shown in Table 1.
A thermal conductivity (25° C.) of the first layer of the surface coating layer in each of the structures in Examples 1 to 4 and Comparative Examples 1 and 2 was measured by use of a laser flash apparatus (thermal constant measuring apparatus: NETZSCH LFA 457 MicroFlash).
In addition, in each of the structures in Examples 1 to 4 and Comparative Examples 1 and 2, the thermal conductivity of the first layer of the surface coating layer was measured before forming the second layer of the surface coating layer.
The thermal conductivity (25° C.) of a base material (stainless steel base material) was measured similarly, and consequently the thermal conductivity of the base material (stainless steel base material) was 25 W/m·K.
The porosity of the first layer of the surface coating layer of each structure was measured from orthogonal cross sections of the structures in Examples 1 to 4 and Comparative Examples 1 and 2, using a scanning electron microscope (manufactured by Hitachi, Ltd., FE-SEM S-4800).
In addition, in the structure in Comparative Example 1, since the first layer of the surface coating layer is composed of a metal (CoNiCrAlY alloy), pores were not present in the first layer of the surface coating layer. Therefore, this was shown by “NS” (Not Specified) in Table 1.
The following heat resistance test was performed to evaluate the heat resistance of the structures in Examples 1 to 4 and Comparative Examples 1 and 2.
Each structure was placed in such a way that the surface coating layer was inclined downward at an angle of 60 degrees from the horizontal and the surface coating layer faced a heating surface of a heater, and the structure was heated by the heater in such a way that a temperature of a center of the outermost surface of the structure (surface coating layer side) became 950° C., and maintained at 950° C. for 60 minutes. Thereafter, at the surface of the base material of each structure, changes in film thickness (dropping downward), and exfoliation or degradation of the surface coating layer were observed. Changes in film thickness of the surface coating layer was checked by use of a film thickness meter, and the exfoliation or degradation of the surface coating layer was visually observed.
In a box of “Heat resistance” in Table 1, in the heat resistance test, the case where any of changes in film thickness (dropping downward), and exfoliation or degradation of the surface coating layer occurred was denoted by “−”, and the case where changes in film thickness (dropping downward), and exfoliation or degradation of the surface coating layer did not occur was denoted by “++”.
In addition, the porosities of the first layer of the surface coating layer of the structures in Examples 1 to 4 and Comparative Examples 1 and 2 were measured before and after a heat resistance test, and consequently it was confirmed that the porosity measured before the heat resistance test was not different from that measured after the heat resistance test in the structures which did not cause changes in film thickness (dropping downward), exfoliation and degradation of the surface coating layer.
The following thermal impact test was performed to evaluate the thermal impact resistance of the structures in Examples 1 to 4 and Comparative Examples 1 and 2.
Each structure was heated at 900° C. in a firing furnace, and then the structure of 900° C. was taken out of the furnace to the outside (room temperature), and forced to be cooled by a fan so that an average temperature drop rate during 2 minutes after taking out the structure was from 200° C./min to 210° C./min. A series of these operations was taken as 1 cycle, and this cycle was repeated 10 times. Thereafter, the presence or absence of peeling of the surface coating layer of the structure was visually observed.
In a box of “Thermal impact resistance” in Table 1, in the thermal impact test, the case where there was peeling in the surface coating layer of the structure was denoted by “−”, and the case where there was no peeling in the surface coating layer of the structure was denoted by “++”.
The following acid corrosion test was performed to evaluate the corrosion resistance of the structures in Examples 1 to 4 and Comparative Examples 1 and 2.
First, was prepared a test solution containing Cl−: 50 ppm, SO32−: 250 ppm, SO42−: 1250 ppm, CO32−: 2000 ppm, NH4+: 1900 ppm, NO2−: 100 ppm, NO3−: 20 ppm, CH3COO−: 400 ppm, HCOO−: 100 ppm, and HCHO: 250 ppm. Next, one structure was fully immersed in a test container containing 50 ml of the above test solution, and each test container was held in an atmosphere of 80° C. to evaporate the test solution completely. The operations were taken as 1 cycle and this cycle was repeated 10 times. Thereafter, the presence or absence of corrosion of the surface coating layer of the structure was visually observed.
In a box of “Corrosion resistance” in Table 1, in the acid corrosion test, the case where the surface coating layer of the structure was degraded and a film thickness decreased was denoted by “−”, the case where the surface coating layer of the structure was degraded but a film thickness did not change was denoted by “+” and the case where the surface coating layer of the structure was not degraded and a film thickness did not change was denoted by “++”.
In the structures in Examples 1 to 4, the second layer containing a crystalline inorganic material (zirconia) having a high softening point is formed as an outermost layer of the surface coating layer. Therefore, even when the structure is exposed to a high-temperature of 950° C., the structure did not cause changes in film thickness (dropping downward), exfoliation and degradation of the surface coating layer, and the surface coating layer of the structure was considered to be prevented from being broken.
Further, in the structures in Examples 1 to 4, peeling of the surface coating layer of the structure in the thermal impact test did not occur, and the surface coating layer of the structure was considered to be prevented from being broken. It is thought that the peeling did not occur since the adhesion between an amorphous inorganic material (glass) composing the first layer of the surface coating layer and a crystalline inorganic material (zirconia) composing the second layer of the surface coating layer of the structure is excellent.
Moreover, since zirconia composing the second layer of the surface coating layer of the structure is a crystalline inorganic material having excellent corrosion resistance, in the structures in Examples 1 to 4, degradation and changes in film thickness of the surface coating layer were considered to be prevented.
In the structure in Comparative Example 1, as with the structures in Examples 1 to 4, the second layer containing a crystalline inorganic material (zirconia) having a high softening point and excellent corrosion resistance is formed as an outermost layer of the surface coating layer. Therefore, the structure in Comparative Example 1 was excellent in heat resistance and corrosion resistance, as with the structures in Examples 1 to 4.
However, in the structure in Comparative Example 1, peeling occurred in the surface coating layer in the thermal impact test. It is thought that the peeling occurred since the adhesion between a metal (CoNiCrAlY alloy) composing the first layer of the surface coating layer of the structure and a crystalline inorganic material (zirconia) composing the second layer of the surface coating layer is low.
In the structure in Comparative Example 2, the second layer containing a crystalline inorganic material (zirconia) having a high softening point is not formed as an outermost layer of the surface coating layer, and a layer containing an amorphous inorganic material (glass) having a low softening point is formed. Therefore, the structure caused changes in film thickness (dropping downward), exfoliation or degradation of the surface coating layer in the heat resistance test, and caused degradation of the surface coating layer of the structure in the acid corrosion test. Moreover, the structure caused peeling of the surface coating layer in the thermal impact test. It is thought that the peeling occurred since the adhesion between a metal (stainless steel) composing the base material and an amorphous inorganic material (glass) composing the first layer of the surface coating layer is low.
In the structures in Examples 1 to 4, the thermal conductivity of the first layer of the surface coating layer is from 0.1 W/m·K to 0.3 W/m·K. Therefore, it is thought that since a difference between the thermal conductivity of the surface coating layer and a thermal conductivity (25 W/m·K) of the base material of the structure is large, the structure has the excellent heat insulating properties. The reason for this is likely that, in the structures in Examples 1 to 4, the first layer of the surface coating layer contains an amorphous inorganic material (glass) with a large porosity and the porosity of the first layer of the surface coating layer is as large as from 30% to 40%.
On the other hand, in the structure in Comparative Example 1, the thermal conductivity of the first layer of the surface coating layer is 2.3 W/m·K. Therefore, it is thought that since a difference between the thermal conductivity of the surface coating layer and a thermal conductivity (25 W/m·K) of the base material of the structure is small, the structure has the poor heat insulating properties. The reason for this is likely that, in the structure in Comparative Example 1, the first layer of the surface coating layer is made of a compact metal (CoNiCrAlY alloy).
In the structure in Comparative Example 2, the thermal conductivity of the first layer of the surface coating layer is 1.0 W/m·K. Therefore, the structure in Comparative Example 2 is superior in heat insulating properties to the structure in Comparative Example 1, but as described above, the structure in Comparative Example 2 is considered to have the problems of heat resistance, thermal impact resistance and corrosion resistance.
From the results described above, it is thought in the structure including a base material made of metal and a surface coating layer formed on the surface of the base material that a structure excellent in heat insulating properties and heat resistance can be prepared by forming a surface coating layer including a first layer which is formed on the surface of the base material and contains an amorphous inorganic material, and a second layer which is formed as an outermost layer of the surface coating layer and contains a crystalline inorganic material having a softening point higher than a softening point of the amorphous inorganic material.
Hereinafter, a second embodiment, which is an embodiment of the structure and the method for manufacturing a structure of the present invention, will be described.
First, a structure of the second embodiment of the present invention will be described.
In the structure of the second embodiment of the present invention, the surface coating layer further includes a third layer including inorganic fibers and a fourth layer containing an amorphous inorganic material, the third layer is formed on the surface of the first layer, and the fourth layer is formed between the third layer and the second layer. Other configurations are the approximately same as in the structure of the first embodiment of the present invention.
The structure 2A shown in
In the structure 2A shown in
The surface coating layer 20e of the structure 2A of the second embodiment of the present invention has a four-layer structure, and specifically, it has a structure in which four layers of the first layer 21a, the third layer 23a, the fourth layer 24a and the second layer 22a are laminated in this order from the side of the base material 10a. In other words, the first layer 21a of the surface coating layer 20e is formed on the surface of the base material 10a. The third layer 23a of the surface coating layer 20e is formed on the surface of the first layer 21a of the surface coating layer 20e and between the first layer 21a and the fourth layer 24a of the surface coating layer 20e. The fourth layer 24a of the surface coating layer 20e is formed on the surface of the third layer 23a of the surface coating layer 20e and between the third layer 23a and the second layer 22a of the surface coating layer 20e. The second layer 22a of the surface coating layer 20e is formed on the surface of the fourth layer 24a of the surface coating layer 20e as the outermost layer of the surface coating layer 20e.
In the structure 2A shown in
Examples of the inorganic fibers composing the third layer of the surface coating layer of the structure include silica-alumina fiber, alumina fiber, silica fiber, zirconia fiber, glass fiber, potassium titanate whisker fiber, rock wool, and inorganic fibers obtained by modifying each of the above-mentioned inorganic fibers so as to contain at least one compound selected from the group consisting of alkali metal compounds, alkaline earth metal compounds and boron compounds. These inorganic fibers are desirable in point of heat resistance, strength and ease of availability. These inorganic fibers may be used singly or in combination of two or more.
Among these inorganic fibers, the alumina fiber and the silica-alumina fiber are desirable from the viewpoint of heat resistance and a handling property.
In addition, the content of alkali metal compound or the like in inorganic fibers obtained by modifying inorganic fibers so as to contain an alkali metal compound or the like is desirably from about 15 wt % to about 40 wt %. Such the inorganic fibers exhibit moderate solubility in normal saline and are safe for environment and ecosystem even when released into the atmosphere.
In the structure of the second embodiment of the present invention, an inorganic powder may be added to the third layer of the surface coating layer as required. When the inorganic powder is added to the third layer of the surface coating layer, the inorganic powder is embraced in a structure of inorganic fibers tangled with one another, and therefore radiation heat transfer and convectional heat transfer is likely to be suppressed and a heat insulating property is likely to be improved.
Further, an inorganic binder may exist in the third layer of the surface coating layer of the structure. When the inorganic binder exists in the third layer of the surface coating layer, since the inorganic fibers are likely to be bonded to one another at a point or plane where inorganic fibers contact with one another in a state of entanglement and are likely to firmly support one another, mechanical strength is likely to be further improved.
Moreover, the third layer of the surface coating layer of the structure may contain a reinforcement member made of metal. When the third layer of the surface coating layer contains a reinforcement member, the inorganic fibers is likely to be held and mechanical strength is likely to be improved. Examples of the reinforcement member include a metal mesh made of the same metal as that composing the base material.
That is, in the structure of the second embodiment of the present invention, the third layer of the surface coating layer may contain at least one of the inorganic powder, the inorganic binder and the reinforcement member in addition to the inorganic fibers.
In addition, in the present specification, the inorganic fiber refers to an inorganic fiber having an aspect ratio of 3 or more. On the other hand, the inorganic powder refers to an inorganic powder having an aspect ratio less than 3. In addition, the aspect ratio refers to a ratio (b/a) of a longer diameter “b” to a shorter diameter “a” of a substance.
In the structure of the second embodiment of the present invention, the third layer of the surface coating layer is formed from an inorganic fibers molded body prepared by molding inorganic fibers etc. into an arbitrary shape by a dry molding process or wet molding process. A method of preparing the inorganic fibers molded body will be described later.
A shape of the inorganic fibers molded body is not particularly limited, and examples thereof include a substantially-flat plate shape, a substantial disk shape, a substantial cube, a substantially rectangular parallelepiped, a substantially cylindrical shape, a substantial donut shape, and a substantially spherical shape.
The base material, the first layer of the surface coating layer and the second layer of the surface coating layer in the structure of the second embodiment of the present invention have the approximately same configurations as in the base material, the first layer of the surface coating layer and the second layer of the surface coating layer in the structure of the first embodiment of the present invention.
Accordingly, a material of the base material, an amorphous inorganic material contained in the first layer of the surface coating layer and a crystalline inorganic material contained in the second layer of the surface coating layer in the structure of the second embodiment of the present invention are as described in the first embodiment of the present invention.
The fourth layer of the surface coating layer of the structure has a configuration similar to the first layer of the surface coating layer. Therefore, the fourth layer of the surface coating layer in the structure of the second embodiment of the present invention has a configuration similar to the first layer of the surface coating layer in the structure of the first embodiment of the present invention.
In the structure of the second embodiment of the present invention, as the first layer and the fourth layer of the surface coating layer, any of the first layer 21b in the structure 1B shown in
In the structure of the second embodiment of the present invention, a shape of the base material may be a substantially semicylindrical shape as with the structure 1E shown in
Further, in the structure of the second embodiment of the present invention, when a substantially semicylindrical-shaped base material is used, the surface coating layer of the structure may be formed on any of the surface on a smaller area side, the surface on a larger area side and the surfaces on both sides.
Moreover, in the structure of the second embodiment of the present invention, when a substantially cylindrical-shaped base material is used, the surface coating layer of the structure may be formed on any of an inner face, an outer face, and outer and inner faces of the base material.
In addition, in the structure of the second embodiment of the present invention, when the surface coating layer is formed on the both faces of the base material, configurations of the surface coating layers of the structure may be the same or different.
In the structure of the second embodiment of the present invention, the thickness of the surface coating layer (total thickness of the first layer, the second layer, the third layer and the fourth layer of the surface coating layer) is desirably from about 501.5 μm to about 12500 μm, and more desirably from about 1040 μm to about 6250 μm.
When the thickness of the surface coating layer of the structure is about 501.5 μm or more, the structure tends to ensure an adequate heat insulating property since the thickness of the third layer of the surface coating layer, which contributes to improvements of heat insulating properties, is not too small. On the other hand, when the thickness of the surface coating layer of the structure is about 12500 μm or less, the surface coating layer is less likely to be vulnerable to peeling off from the base material since the thickness of the surface coating layer is not too large relative to the thickness of the base material. Further, when the thickness of the surface coating layer of the structure is about 12500 μm or less, the surface coating layer of the structure is less likely to be vulnerable to a break since a degree of thermal impact to the surface coating layer of the structure hardly increases.
In the structure of the second embodiment of the present invention, the thickness of the third layer of the surface coating layer is desirably from about 500 μm to about 10000 μm, and more desirably from about 1000 μm to about 5000 μm.
When the thickness of the third layer of the surface coating layer of the structure is about 500 μm or more, the structure tends to achieve the adequate effect of heat insulation by providing the third layer. Further, when the thickness of the third layer of the surface coating layer of the structure about 10000 μm or less, the heat insulating properties of the structure is hardly improved, but since the adhesion of the third layer to another layer is low, if the thickness of the third layer is not too large, the third layer is less likely to be vulnerable to peeling off, and thereby the surface coating layer of the structure is likely to be retained.
In the structure of the second embodiment of the present invention, a desired thickness of the first layer of the surface coating layer, a desired thickness of the second layer of the surface coating layer, and the total thickness of the first layer and the second layer of the surface coating layer are as described in the first embodiment of the present invention.
Further, in the structure of the second embodiment of the present invention, a desired thickness of the fourth layer of the surface coating layer is similar to a desired thickness of the first layer of the surface coating layer.
Next, a method for manufacturing a structure of the second embodiment of the present invention will be described.
In the method for manufacturing the structure of the second embodiment of the present invention, the process of forming the surface coating layer further includes:
a process of forming a third layer of the surface coating layer, including inorganic fibers, on the surface of the first layer of the surface coating layer; and
a process of forming a fourth layer of the surface coating layer, containing an amorphous inorganic material, between the third layer of the surface coating layer and the second layer of the surface coating layer.
Specifically, in the process of forming the surface coating layer, the first layer of the surface coating layer is formed on the surface of the base material, the third layer of the surface coating layer is formed on the surface of the first layer of the surface coating layer, the fourth layer of the surface coating layer is formed on the surface of the third layer of the surface coating layer, and the second layer of the surface coating layer is formed on the surface of the fourth layer of the surface coating layer.
Other processes in the method for manufacturing the structure of the second embodiment of the present invention are similar to those in the method for manufacturing the structure of the first embodiment of the present invention.
Herein, an example of methods for manufacturing the structure of the second embodiment of the present invention will be described, taking, as an example, the case where an inorganic fibers molded body to become a third layer of the surface coating layer is prepared in advance and the first layer, the third layer and the fourth layer of the surface coating layer are collectively formed.
(1) Process of Preparing Base Material Made of Metal
Starting from a base material (metal base material) made of metal, first, a cleaning process is performed in order to remove impurities on the surface of the metal base material.
Further, after the cleaning process, as required, the surface of the metal base material may be subjected to a roughening process in order to increase a specific surface area of the surface of the metal base material or to adjust the surface roughness of the metal base material. After the roughening process, a cleaning process may be further carried out.
Specific methods of the cleaning and roughening processes are as described in the first embodiment of the present invention.
(2) Process of Preparing Inorganic Fibers Molded Body
An inorganic fibers molded body to become a third layer of the surface coating layer is prepared by molding inorganic fibers etc. into an arbitrary shape by a dry molding process or wet molding process.
When the inorganic fibers molded body is prepared by a dry molding process, inorganic fibers and, as required, an inorganic powder and/or an inorganic binder were charged into a mixer such as V-type mixer in a predetermined proportion and adequately mixed. Thereafter, the mixture was charged into a predetermined die and pressed to obtain an inorganic fibers molded body. The mixture may be heated during pressing as required.
The inorganic fibers molded body is usually substantially flat plate-shaped, but is not limited to this shape, and may be a shape in which a plate-like body is stacked vertically.
On the other hand, when the inorganic fibers molded body is prepared by a wet molding process, inorganic fibers and, as required, an inorganic powder and/or an inorganic binder were mixed and stirred in water to adequately disperse. Thereafter, an aqueous solution of aluminum sulphate was added as an agglomerating agent to obtain a primary agglomerate in which the inorganic powder and/or inorganic binder is attached to the inorganic fibers. Next, an emulsion of an organic elastic material is added to water, as required, to a predetermined extent, and a cationic polymer agglomerating agent is added to obtain slurry (suspension) containing an agglomerate.
Subsequently, the slurry (suspension) containing the agglomerate is screened with a network material (mesh) and produced by a sheet-forming process to obtain a substantially flat plate-shaped sheet produced by a sheet-forming process. Thereafter, the resulting sheet was dried to obtain an inorganic fibers molded body. Further, after producing by a sheet-forming process, a density of the sheet may be increased by pressing a whole body.
(3) Process of Collectively Forming First Layer, Third Layer and Fourth Layer of Surface Coating Layer
First, a raw material composition for the first layer of the surface coating layer is prepared, and the surface of the metal base material is coated with the raw material composition for the first layer of the surface coating layer.
A method of preparing the raw material composition for the first layer of the surface coating layer, and a method of coating the metal base material with the raw material composition for the first layer of the surface coating layer are as described in the first embodiment of the present invention.
Next, the inorganic fibers molded body prepared in the above process (2) is placed on the raw material composition for the first layer of the surface coating layer applied onto the surface of the metal base material.
In this time, since the raw material composition for the first layer of the surface coating layer is in the form of slurry, it is desirable to immerse a part of the inorganic fibers molded body in the raw material composition for the first layer of the surface coating layer.
Moreover, a reinforcement member such as a metal mesh may be added to the inorganic fibers molded body.
Subsequently, the raw material composition for the fourth layer of the surface coating layer is prepared, and the surface of the inorganic fibers molded body, which is placed on the metal base material and the raw material composition for the first layer of the surface coating layer, is coated with the raw material composition for the fourth layer of the surface coating layer. Thereby, the inorganic fibers molded body is sandwiched between the raw material composition for the first layer of the surface coating layer and the raw material composition for the fourth layer of the surface coating layer.
Then, the metal base material, on which the raw material composition for the first layer of the surface coating layer, the inorganic fibers molded body and the raw material composition for the fourth layer of the surface coating layer are laminated in this order from the metal base material side, is subjected to a firing process.
By the procedure described above, the first layer, the third layer and the fourth layer of the surface coating layer are collectively formed on the metal base material.
In addition, as the raw material composition for the fourth layer of the surface coating layer, the same composition as in the raw material composition for the first layer of the surface coating layer can be employed. The raw material that is different in composition from the raw material composition for the first layer of the surface coating layer may be used.
A method of preparing the raw material composition for the fourth layer of the surface coating layer, and a method of coating the inorganic fibers molded body with the raw material composition for the fourth layer of the surface coating layer are the approximately same as in the method for forming the first layer of the surface coating layer.
Further, a specific method of firing process is as described in the first embodiment of the present invention.
(4) Process of Forming Second Layer of Surface Coating Layer
A second layer of the surface coating layer, containing a crystalline inorganic material having a softening point of about 950° C. or higher, is formed on the surface of the fourth layer of the surface coating layer formed in the above process (3).
Specific method of forming the second layer of the surface coating layer are as described in the first embodiment of the present invention.
By the above procedure, a structure of the second embodiment of the present invention can be manufactured.
In addition, the structure of the second embodiment of the present invention may be manufactured by forming the first layer, the third layer and the fourth of the surface coating layer independently on the metal base material. In this case, after the first layer of the surface coating layer is formed, an inorganic fibers molded body may be placed on the first layer of the surface coating layer using an adhesive or the like.
In the second embodiment of the present invention, the effects (1) to (6) described in the first embodiment of the present invention can be exerted and the following effect can be exerted.
(7) In the structure of the present embodiment, the surface coating layer further includes a third layer including inorganic fibers and a fourth layer containing an amorphous inorganic material, the third layer is formed on the surface of the first layer, and the fourth layer is formed between the third layer and the second layer.
The third layer of the surface coating layer is likely to have a very large porosity since it includes inorganic fibers. Accordingly, a thermal conductivity of the surface coating layer is likely to be significantly decreased. As a result of this, since a difference between the thermal conductivity of the surface coating layer and a thermal conductivity of the base material is likely to be increased, the heat insulating properties of the structure is likely to be more improved.
Hereinafter, a third embodiment which is an embodiment of the structure of the present invention will be described, in reference to drawings.
The structure of the third embodiment of the present invention is an exhaust pipe used as a member composing an exhaust system connected to an internal combustion engine such as an automobile engine. A configuration of the structure of the third embodiment of the present invention is the same as that of the structure of the first embodiment or the second embodiment of the present invention except that the base material is a tubiform as an essential configuration.
Specifically, the structure of the third embodiment of the present invention is likely to be suitably used, for example, as an exhaust manifold.
Hereinafter, the structure of the third embodiment of the present invention will be described, taking an exhaust manifold connected to an internal combustion engine such as an automobile engine as an example.
Further,
As shown in
A cylinder head 102 is mounted on a top of a cylinder block 101 of the automobile engine 100. The exhaust manifold 110 is attached to one side of the cylinder head 102.
The exhaust manifold 110 has a shape like a glove and includes branched pipes 111a, 111b, 111c and 111d corresponding to the number of cylinders, and a collecting part 112 combining the branched pipes 111a, 111b, 111c and 111d into one.
Moreover, a catalytic converter including a catalyst supporting carrier is connected to the exhaust manifold 110. The exhaust manifold 110 has a function of collecting exhaust gases from the respective cylinders and sending the exhaust gases to the catalytic converter.
Then, the exhaust gases G (in
As shown in
In the exhaust manifold 110 (structure of the third embodiment of the present invention) shown in
Further, the surface coating layer 130 has a first layer 131 containing an amorphous inorganic material and a second layer 132 containing a crystalline inorganic material.
In the structure (exhaust manifold) of the third embodiment of the present invention, a similar configuration to those of the surface coating layers in the structures described in the first embodiment and the second embodiment can be employed as the configuration of the surface coating layer.
An example of a surface coating layer, which has a similar configuration to that of the surface coating layer 20a in the structure 1A shown in
In the structure (exhaust manifold) of the third embodiment of the present invention, the surface coating layer is desirably formed on the entire inner face of the base material. The reason for this is that an area of the surface coating layer contacting with the exhaust gases is maximized and the structure is excellent in heat resistance. However, the surface coating layer may be formed only on a part of the inner face of the base material.
Further, in the structure of the third embodiment of the present invention, the surface coating layer may be formed on the outer face in addition to the inner face, or may be formed only on the outer face.
An example of the exhaust manifold has been described as the structure of the third embodiment of the present invention, but the application of the structure of the third embodiment of the present invention is not limited to the exhaust manifold, and it is likely to be suitably used as an exhaust pipe, a pipe composing the catalytic converter, a turbine housing or the like.
When the structure of the third embodiment of the present invention is manufactured, it can be manufactured in the approximately same manner as in the structure of the first embodiment or the second embodiment of the present invention except that the shape of the base material is different.
In addition, in the structure of the third embodiment of the present invention, when the surface coating layer is formed on the inner face of the base material, as described in the first embodiment of the present invention, it is preferred to use the base material composed of the first half-cut member and the second half-cut member.
Also in the third embodiment of the present invention, the effects (1) to (6) described in the first embodiment of the present invention, and the effect (7) described in the second embodiment of the present invention can be exerted.
In the structure of the first embodiment of the present invention, the first layer of the surface coating layer is formed on the surface of the base material, and the second layer of the surface coating layer is formed on the surface of the first layer of the surface coating layer. Further, in the structure of the second embodiment of the present invention, the first layer of the surface coating layer is formed on the surface of the base material, the third layer of the surface coating layer is formed on the surface of the first layer of the surface coating layer, the fourth layer of the surface coating layer is formed on the surface of the third layer of the surface coating layer, and the second layer of the surface coating layer is formed on the surface of the fourth layer of the surface coating layer.
However, in the structure according to the embodiments of the present invention, a configuration between the first layer and the second layer of the surface coating layer is arbitrary as long as the first layer of the surface coating layer is formed on the surface of the base material and the second layer of the surface coating layer is formed as the outermost layer of the surface coating layer.
However, in the case where the structure according to the embodiments of the present invention is used as an exhaust pipe, when the surface coating layer is formed on an inner face of the tubiform, if many layers are present between the first layer and the second layer of the surface coating layer, a diameter of the exhaust pipe is likely to become small, and the exhaust gases become hard to pass. Accordingly, when the structure according to the embodiments of the present invention is used as an exhaust pipe, the surface coating layer preferably has a two-layer configuration consisting of the first layer and the second layer.
When the raw material composition for the first layer of the surface coating layer, which is used in manufacturing the structure according to the embodiments of the present invention, contains the crystalline inorganic material and the amorphous inorganic material, a mixed amount of the amorphous inorganic material has a desired lower limit of about 50 wt % and a desired upper limit of about 99.5 wt % with respect to a total weight of a powder of the amorphous inorganic material and a powder of the crystalline inorganic material.
When the mixed amount of the amorphous inorganic material contained in the first layer of the surface coating layer of the structure is about 50 wt % or more, since the amount of the amorphous inorganic material contributing to the adhesion between the surface coating layer and the base material of the structure is not too small, the surface coating layer hardly exfoliate in the structure manufactured. On the other hand, when the mixed amount of the amorphous inorganic material contained in the first layer of the surface coating layer of the structure about 99.5 wt % or less, since the amount of the crystalline inorganic material is not too small, the adequate effect of improving the adhesion between the surface coating layer and the base material of the structure tends to be achieved. The mixed amount of the amorphous inorganic material contained in the raw material composition for the first layer of the surface coating layer has a more desired lower limit of about 60 wt % and a more desired upper limit of about 95 wt %.
When the raw material composition for the first layer of the surface coating layer, which is used in manufacturing the structure according to the embodiments of the present invention, contains the crystalline inorganic material and the amorphous inorganic material, a mixed amount of the crystalline inorganic material has a desired lower limit of about 0.5 wt % and a desired upper limit of about 50 wt % with respect to a total weight of a powder of the amorphous inorganic material and a powder of the crystalline inorganic material.
When the mixed amount of the crystalline inorganic material contained in the first layer of the surface coating layer of the structure is about 0.5 wt % or more, since the amount of the crystalline inorganic material contributing to the adhesion between the surface coating layer and the base material of the structure is not too small, the adequate effect of improving the adhesion between the surface coating layer and the base material of the structure tends to be achieved. On the other hand, when the mixed amount of the crystalline inorganic material contained in the first layer of the surface coating layer of the structure about 50 wt % or less, the amount of the amorphous inorganic material contributing to the adhesion between the surface coating layer and the base material of the structure is not too small, and the surface coating layer hardly exfoliate in the structure manufactured.
Examples of the dispersion medium capable of being mixed in the raw material composition for the first layer of the surface coating layer, which is used in manufacturing the structure according to the embodiments of the present invention, include water and organic solvents such as methanol, ethanol, acetone and the like. A mixing ratio of the mixed powder or the powder of the amorphous inorganic material, which are respectively contained in the raw material composition for the first layer of the surface coating layer, to the dispersion medium is not particularly limited, but it is desired, for example, that the amount of the dispersion medium is from about 50 parts by weight to about 150 parts by weight with respect to 100 parts by weight of the mixed powder or the powder of the amorphous inorganic material. The reason for this is that this mixing ratio is likely to yield viscosity suitable for application to the base material.
Examples of the organic binder capable of being mixed in the raw material composition for the first layer of the surface coating layer include polyvinyl alcohol, methylcellulose, ethylcellulose, carboxymethylcellulose, and the like. These may be used singly or in combination of two or more of them.
Further, the dispersion medium and the organic binder may be used in combination.
In the structure according to the embodiments of the present invention, a shape of the base material may be a substantially flat plate, a substantially semicylindrical shape, a substantially cylindrical shape, and a profile of its cross section may be any shape, for example, a substantial ellipse, a substantially polygonal shape, etc.
When the base material of the structure is a tubiform, a diameter of the base material does not have to be substantially constant along a longitudinal direction, and a shape of a cross section substantially perpendicular to a length direction does not have to be substantially constant along a longitudinal direction.
When the structure according to the embodiments of the present invention is used as an exhaust manifold, the number of branched pipes composing the exhaust manifold may be equal to the number of engine cylinders and it is not particularly limited.
In addition, examples of the cylinder of the engine include a single cylinder, 2 cylinders, 4 cylinders, 6 cylinders and 8 cylinders.
In the structure according to the embodiments of the present invention, a desired lower limit of the thickness of the base material is about 0.2 mm, and a more desired lower limit of the thickness of the base material is about 0.4 mm, and a desired upper limit is about 10 mm and a more desired upper limit is about 4 mm.
When the thickness of the base material of the structure is about 0.2 mm or more, strength of the structure is hardly insufficient. When the thickness of the base material of the structure is about 10 mm or less, a weight of the structure is not too large, and therefore it hardly becomes difficult to mount the structure on vehicles such as automobiles and the structure is likely to be suitable for practical use.
In the structure according to the embodiments of the present invention, the surface of the base material may be a roughened surface at which bumps and dips are formed.
In this case, the surface roughness RzJIS of the roughened surface of the base material of the structure is preferably from about 1.5 μm to about 15 μM.
The surface roughness RzJIS of the roughened surface of the base material of the structure is ten-point mean roughness defined by JIS B 0601 (2001).
When the surface roughness RzJIS of the roughened surface of the base material of the structure is about 1.5 μm or more, adequate adhesion between the base material and the surface coating layer tends to be attained since a surface area of the base material is not too small. On the other hand, when the surface roughness RzJIS of the roughened surface of the base material of the structure is about 15 μm or less, the surface coating layer tends to be easily formed on the surface of the base material. The reason for this is likely that if the surface roughness RzJIS of the roughened surface of the base material of the structure is too large, slurry (raw material composition for the first layer of the surface coating layer) does not penetrate into a valley portion of bumps and dips formed at the surface of the base material to produce voids there.
In addition, the surface roughness RzJIS of the roughened surface of the base material of the structure can be measured according to JIS B 0601 (2001) by use of HANDY SURF E-35B manufactured by Tokyo Seimitsu Co., Ltd.
The contents of JIS B 0601 (2001) are incorporated herein by reference in their entirety.
In the structure according to the embodiments of the present invention, the surface coating layer does not necessarily have to be formed on the entire surface of the base material.
For example, when the structure according to the embodiments of the present invention is used as an exhaust pipe, the surface coating layer may be formed on the inner face of the tubiform as a base material. When the surface coating layer is formed on the inner face of the tubiform as a base material, the surface coating layer do not have to be formed on the entire inner face of the tubiform as a base material, and the surface coating layer may be formed on at least an area with which the exhaust gases contact directly.
In the structure according to the embodiments of the present invention, when the surface coating layer includes the third layer, a shape of a cross section of the inorganic fibers composing the third layer of the surface coating layer is not particularly limited, and examples thereof include a substantially circular cross section, a substantially planiform cross section, a hollow cross section, a substantially polygonal cross section and a substantially core-sheath cross section. Among these, a modified cross-section fiber having a hollow cross section, a substantially planiform cross section or a substantially polygonal cross section can be suitably used since they are likely to have many occasions to reflect radiation heat transfer in heat transfer and heat insulating properties are likely to be improved.
In the structure according to the embodiments of the present invention, when the surface coating layer includes the third layer, a desired lower limit of an average fiber length of the inorganic fibers composing the third layer of the surface coating layer is about 0.1 mm, and a more desired lower limit is about 0.5 mm. On the other hand, a desired upper limit of an average fiber length of the inorganic fibers is about 50 mm, and a more desired upper limit is about 10 mm.
When an average fiber length of the inorganic fibers contained in the third layer of the surface coating layer of the structure is about 0.1 mm or more, fibers tend to tangle with one another and mechanical strength of the resulting third layer of the surface coating layer hardly deteriorates. On the other hand, when an average fiber length of the inorganic fibers contained in the third layer of the surface coating layer of the structure is about 50 min or less, the effect of reinforcing the surface coating layer is hardly achieved, but the inorganic fibers are likely to closely tangle with one another or single inorganic fibers hardly alone curl. Therefore, continuous cavity is hardly produced, and therefore, heat insulating properties hardly deteriorate.
In the structure according to the embodiments of the present invention, when the surface coating layer includes the third layer, a desired lower limit of an average fiber diameter of the inorganic fibers composing the third layer of the surface coating layer is about 1 μm, and a more desired lower limit is about 2 μm. On the other hand, a desired upper limit of an average fiber diameter of the inorganic fibers is about 10 μm, and a more desired upper limit is about 5 μm.
When an average fiber diameter of the inorganic fibers contained in the third layer of the surface coating layer of the structure is about 1 μm or more, mechanical strength of the inorganic fibers theirself hardly deteriorates. On the other hand, when an average fiber diameter of the inorganic fibers contained in the third layer of the surface coating layer of the structure is about 10 μm or less, solid heat transfer through the inorganic fibers hardly increases, and heat insulating properties hardly deteriorate.
In the structure according to the embodiments of the present invention, when the surface coating layer includes the third layer, the third layer of the surface coating layer may further include an inorganic powder.
Examples of the inorganic powder contained in the third layer of the surface coating layer of the structure include TiO2 powder, BaTiO3 powder, PbS powder, SiO2 powder, ZrO2 powder, SiC powder, NaF powder, LiF powder, and the like. These inorganic powders may be used singly or in combination of two or more.
When the inorganic powders are used in combination, examples of preferred combinations include a combination of TiO2 powder and SiO2 powder, a combination of TiO2 powder and BaTiO3 powder, a combination of SiO2 powder and BaTiO3 powder and a combination of TiO2 powder, SiO2 powder, and BaTiO3 powder.
In the structure according to the embodiments of the present invention, when the surface coating layer includes the third layer, the third layer of the surface coating layer may include an inorganic binder for the purpose of maintaining strength at elevated temperature.
Examples of the inorganic binder contained in the third layer of the surface coating layer of the structure include colloidal silica, synthesized mica, montmorillonite, and the like. These inorganic binders may be used singly or in combination of two or more.
With respect to an aspect of use of the inorganic binder, the inorganic binder can be mixed in a raw material, or the resulting inorganic fibers molded body can be impregnated with the inorganic binder.
In the structure according to the embodiments of the present invention, it is an essential constituent that the structure includes a base material made of metal and a surface coating layer formed on the surface of the base material and that the surface coating layer includes a first layer which is formed on the surface of the base material and contains an amorphous inorganic material, and a second layer which is formed as an outermost layer of the surface coating layer and contains a crystalline inorganic material having a softening point of about 950° C. or higher.
The desired effects is likely to be achieved by appropriately combining various configurations (e.g., configuration of the first layer of the surface coating layer, shape of the base material, exhaust manifold) which have been described in detail in the first embodiment to third embodiment of the present invention and other embodiments of the present invention with the essential constituent.
Obviously, numerous modifications and variations of the present invention are possible in light of the above teachings. It is therefore to be understood that within the scope of the appended claims, the invention may be practiced otherwise than as specifically described herein.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2011-026387 | Feb 2011 | JP | national |
The present application is a divisional application of the U.S. patent application Ser. No. 13/368,336 filed Feb. 8, 2012, which claims priority to Japanese Patent Application No. 2011-026387, filed Feb. 9, 2011. The contents of these applications are incorporated herein by reference in their entirety.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 13368336 | Feb 2012 | US |
| Child | 14321753 | US |
