The present invention relates to a piston for an internal combustion engine and a method of manufacturing a piston for an internal combustion engine.
Hitherto, there has been known a piston for an internal combustion engine in which a particular region that constitutes a part of a crown surface of the piston, that includes a fuel collision portion with which a fuel collides in a liquid state, and that includes a main combustion region is comprised of a member or structure having a low thermal conductivity and a low specific heat. According to this configuration, it is said that a temperature-raising effect at the fuel collision part can be enhanced, the combustion of the fuel colliding against the piston can be thereby promoted, deposition of the fuel on the piston crown surface can be reduced, and discharge of deposits and smoke can be restrained (Patent Document 1).
However, in the piston for an internal combustion engine disclosed in Patent Document 1, there is no description in regard of a specific method for configuring the member having the low thermal conductivity. In addition, there is a problem that the joining or adhesive strength at the interface between the low-thermal-conductivity member and the piston base material may be insufficient, due to a temperature distribution generated between the low-thermal-conductivity member and the piston base material.
In accordance with a first mode of the present invention, a piston for an internal combustion engine is provided with a surface treatment portion on a piston base material at a piston crown surface, the surface treatment portion including, along a direction of depth from a surface side, a first layer that is comprised of a layer of a first metal or a layer containing the first metal, a second layer that contains both a second metal containing oxygen or an oxide of the second metal and a low-thermal-conductivity material, and a third layer that is comprised of a mixture of a third metal and the low-thermal-conductivity material.
In accordance with a second mode of the present invention, a method of manufacturing a piston for an internal combustion engine is a method of manufacturing a piston for an internal combustion engine provided with a surface treatment portion at a crown surface, in which a step of forming the surface treatment portion includes, at least: a recess forming step of forming a recess in the crown surface of a piston base material of the piston; a first filling step of filling the recess with a first molding material which is a powder or a green compact of a powder; a first stir joining step of bringing a rotary tool into contact with the first molding material to soften the first molding material by frictional heat, thereby achieving solid-phase joining of the first molding material to the recess, and forming a stirred portion of the first molding material and the piston base material; a second filling step of filling a region over a formed layer formed by solid-phase joining in the first stir joining step with a second molding material which is a powder or a green compact of a powder; and a second stir joining step of bringing a rotary tool into contact with the second molding material to soften the second molding material by frictional heat, thereby achieving solid-phase joining of the second molding material to the recess, and forming a stirred portion of the second molding material and the piston base material.
According to the present invention, by providing the surface treatment portion configured as aforementioned, it is possible to provide a piston for an internal combustion engine in which discharge of deposits and smoke is restrained and a favorable fuel cost is obtained owing to excellent heat insulating characteristic. In addition, since the surface treatment portion and the piston base material are firmly joined to each other, it is possible to provide a piston for an internal combustion engine that is excellent in durability.
Embodiments of the present invention will be described below, referring to the drawings.
A piston for an internal combustion engine is normally manufactured by processing a metal represented by an aluminum alloy. At a piston crown surface, for promoting combustion of a fuel, it is desired that a region concerning the combustion is sufficiently heat insulated to prevent temperature from being lowered at the time of combustion. In the case where a coating layer is formed on the piston crown surface by using only a low-thermal-conductivity material having a high heat insulating characteristic, however, there is a problem that adhesion or joining property between the low-thermal-conductivity material and the piston base material is insufficient, and it is impossible to secure a joining strength at the interface between both the materials.
In addition, for promoting combustion of the fuel in the vicinity of the piston crown surface, the region concerning the combustion should be uniformly raised in temperature. In the case where a coating layer is formed on the piston crown surface by using only a low-thermal-conductivity material having a high heat insulating characteristic, however, there is a problem that a region where temperature is locally raised tends to be generated on the surface of the coating layer.
In relation to this point, in the case where a single layer of a composite material of a metal and a low-thermal-conductivity material is formed on the piston crown surface, a sufficient joining strength can be obtained between the thus formed layer and the piston base material, and heat generated by combustion is conducted through the inside of the piston base material, so that the piston crown surface can be heated uniformly. However, there is a problem that the thermal conduction inside the piston base material is high, and, consequently, heat insulating characteristic becomes insufficient, so that the piston crown surface cannot be kept at a sufficiently high temperature.
In view of this, as shown in
The metal used for the third layer is preferably any one of aluminum, magnesium, iron, copper, zinc, titanium, and nickel or an alloy containing at least one of these metals. These metals are metals that can undergo solid-phase joining to a metallic material used as the piston base material, whereby a high joining strength is easily obtained in relation to the piston base material.
As above-mentioned, the piston base material is ordinarily an aluminum alloy, and, therefore, the metal used for the third layer making contact with the piston base material is preferably aluminum or an aluminum alloy. Aluminum or an aluminum alloy can obtain a high joining strength in relation to the aluminum alloy by a solid-phase joining method. Besides, the metal used for the first layer is also preferably aluminum or an aluminum alloy. As a result of this, the first layer and the third layer ensure that joining to the piston base material, which is an aluminum alloy, with a high adhesive strength can be obtained by a solid-phase joining method, and a uniform heating condition can be easily obtained at a surface layer of the surface treatment portion.
A metal contained in the state of containing oxygen or in the state of an oxide, of a second layer, is preferably the same as a metal contained in a third layer. In the piston for an internal combustion engine according to the embodiment of the present invention, a configuration may be adopted where the crown surface is shaped to have a recess, and a surface treatment portion is provided in the structure of filling the recessed surface.
In the piston for an internal combustion engine in each of the above embodiments, a connection portion where a side surface and a bottom surface contact each other, in the recess formed in the piston crown surface 11 for forming the surface treatment portion, is preferably comprised of a curved surface. With such a curved surface configured, favorable solid-phase joining of a molding material can be achieved over the whole region of the recess. In the case where this portion is not a curved surface, the molding material would be left at the connection portion in the state of not having undergone solid-phase adhesion, thereby causing generation of a portion of inadequate solid-phase joining.
The second layer is preferably thicker at a peripheral portion than at a central portion. At a peripheral portion of a piston, conduction of heat to a piston side surface is generated. With the second layer formed to be thicker at a peripheral portion than at a central portion, conduction of heat to the piston side surface can be restrained, and a heat insulating effect can be enhanced. In addition, a structure having a stirred portion is preferably provided at an outer peripheral portion of the surface treatment portion. The stirred portion refers to a portion where a flow of composition of material has occurred. An outer peripheral portion of the surface treatment portion has a tendency that it is difficult to secure a joining strength, but, when a region where the material of the piston base material and the material of the surface treatment portion have been stirred is provided, the joining strength can be secured thereby.
While a sufficient heat insulating effect can be obtained even where the second layer is a single layer, a higher heat insulating effect can be expected favorably in a configuration in which a plurality of the second layers are provided. The area of the surface treatment portion is preferably smaller on a lower portion side (lower portion side) than on the piston crown surface side (upper portion side).
The position where the surface treatment portion is formed is not particularly limited, but the position is preferably at the piston crown surface in the vicinity of a region where the fuel is injected. In the region where the fuel is injected, the liquid fuel is evaporated and combusted, and, therefore, by forming the surface treatment portion at this position, it is possible to enhance a combustion promoting effect.
The low-thermal-conductivity material is not particularly restricted, but it is preferable to use any one, or a plurality in combination, of zirconia, cordierite, mullite, silicon, silica, mica, talc, silicate glass, acrylic glass, organic glass, silica aerogel, hollow ceramic beads, hollow glass beads, hollow metal balls, organosilicon compound, and ceramic fiber.
In the second layer and the third layer, the volume ratio of the low-thermal-conductivity material contained therein is preferably equal to or more than 45%. In the case where the volume ratio of the low-thermal-conductivity material is equal to or more than 45%, a high heat insulating characteristic can be obtained, and, therefore, the piston crown surface can be raised in temperature in a shorter time, whereby a higher combustion promoting effect can be expected.
In step S3, the recess formed in the piston crown surface is filled with a material for forming the surface treatment portion. In this case, the material may be used for filling in the state of a powder, or a pressure may be exerted on the powder to produce a green compact (briquet) and the green compact may be used for filling.
Next, in step S4, in a state in which a rotary tool is put in contact with the material filling the recess, the rotary tool is rotated for a predetermined time. Subsequently, in step S5, the rotary tool is drawn out of the recess. By the series of steps from step S3 to step S5, friction stir welding (FSW: Friction-Stir-Welding) is performed. The steps from step S3 to step S5 are repeated a number of times according to the number of layers required. The friction stir welding will be described in detail later.
In step S6, the piston formed with the surface treatment portion is taken out, and subjected to a heat treatment. This heat treatment is for the purpose of removing strains generated attendant on plastic flow of the material during the friction stir welding and making the surface treatment portion uniform in strength. Examples of the heat treatment include a solution aging treatment and an artificial aging treatment. After the heat treatment is conducted in step S6, secondary machining is performed in step S7. As the secondary machining, finishing cutting is conducted, whereby a piston as a product is completed.
Steps S3 to S5 will be described in detail. In step S3, first, the recess in the piston crown surface is filled with the material for forming the third layer of the surface treatment portion. Next, the rotary tool is rotated as above-mentioned in step S4, after which the rotary tool is drawn out of the recess in step S5. By this, the third layer is formed. In this instance, a surface layer of the third layer becomes the second layer. Next, returning to step S3, a region over the second layer is filled with the material for forming the first layer. Subsequently, the rotary tool is rotated in step S4, after which the rotary tool is drawn out of the recess in step S5. By this, the first layer is formed on the second layer. Note that the process of formation of the second layer will be described in detail later.
As above-mentioned, the steps S3 to S5 are repeated as required according to the configuration of the surface treatment portion to be formed. For example, in the case of a configuration in which the third layer and the second layer are alternately repeated as shown in
In the next place, the friction stir welding will be described. The friction stir welding is one of solid-phase joining techniques for joining a metal and a metal to each other. In order to perform the friction stir welding, a rotary tool is rotated in the state of being pressed against a metallic material to be joined, to heat the metallic material by frictional heat generated, and to cause a flow of composition in the metallic material (or to stir the metallic material), thereby joining the metallic material.
As another method for joining metallic materials, there are also fusion welding methods such as arc welding. In the fusion welding method, however, the metallic material undergoes a process of melting followed by solidification, so that a structure attendant on the solidification is formed in the weld joint, which would cause deterioration of strength characteristic or the like. On the other hand, in the friction stir welding, melting (fusion) and solidification of the material do not occur, so that the strength problem as above-mentioned is not generated, and the material can be joined more firmly. The surface treatment portion according to the present invention is preferably formed by friction stir welding.
In addition, according to friction stir welding, in an oxygen-containing environment such as in the air, a metallic material can be joined with little adverse influence exerted on joining strength by oxidation of the material. According to the friction stir welding, not only metallic materials but also other metal-containing materials can be joined without generation of defective bonding attendant on oxidation of the material at the joint portion.
In friction stir welding, when the rotary tool is rotated in contact with the material to be joined, a state in which oxygen is liable to be bonded to the metal contained in the material is generated at the surface of the material with which the rotary tool is in contact. For this reason, a surface layer portion of the joined layer is a layer of another composition that contains either a metal containing oxygen or an oxide of the metal.
Specifically, at the time of forming the third layer by the first-time friction stir welding step, the surface layer portion of the third layer becomes a layer of a mixture of a metal containing oxygen or an oxide of the metal with the low-thermal-conductivity material. In other words, the second layer can be formed simultaneously. Thereafter, the first layer can be formed by second-time friction stir welding.
Therefore, a region containing much oxygen may be formed also at a surface layer portion of the first layer of the surface treatment portion. In the case where such a region has been formed, it can be removed by cutting, which is shown as a secondary machining step. Note that where the friction stir welding step for the outermost surface layer (first layer) is conducted in a non-oxygen-containing atmosphere such as argon gas or vacuum, formation of an oxygen-containing region can be restrained thereby.
In the first-time material filling step, a mixed powder containing the metal and the low-thermal-conductivity material or a green compact of the mixed powder is used. By this, the third layer in which the low-thermal-conductivity material is dispersed can be formed, as shown in
In the fusion welding method such as arc welding, there is a problem that when it is intended to form the surface treatment portion by use of a mixed powder or a green compact thereof, the metal and the low-thermal-conductivity material would separate from each other, since they are different in melting point and specific gravity. In this point, also, the formation of the surface treatment portion by friction stir welding which has a mechanical stirring action makes it possible to form a layer in which the metal and the low-thermal-conductivity material are dispersed uniformly throughout the layer.
In the case where the friction stir welding is conducted using a material obtained by mixing a metallic powder with a low-thermal-conductivity material powder, only the metallic powder is joined to the piston base material, whereby the layer formed is fixed to the piston base material. In other words, the low-thermal-conductivity material and the piston base material are not joined directly to each other. In determining the content ratio of the low-thermal-conductivity material, therefore, attention should be paid to the joining strength. According to the present inventors' research, it is preferable that the volume ratio of the low-thermal-conductivity material in the mixed powder is equal to or less than 80%. Where the volume ratio exceeds 80%, the joining strength may be insufficient, and the surface treatment portion once formed may peel off.
A specimen deemed as a piston crown surface is produced, and a surface treatment portion is formed at a surface of the specimen. A disk-shaped specimen was produced from an aluminum alloy (4032-T6) similar to the material of a piston base material, and a recess measuring 30 mm in diameter and 5 mm in depth was formed in an upper surface of the specimen. After the recess was filled with a predetermined amount of a powder 51, a load was applied while rotating a rotary tool with a diameter of 30 mm at 800 rpm, to press the powder 51 into the recess of the specimen. The rotary tool was held for a predetermined time in such a state that the lower end of the rotary tool was positioned at a height of 1.5 mm from the lower surface of the recess, after which the rotary tool was drawn out of the recess.
Next, the recess was filled with a predetermined amount of a powder 52, and a load was applied while rotating a rotary tool with a diameter of 34 mm at 800 rpm. By this, the powder 52 was pressed in by the rotary tool while crushing the periphery of the recess of the specimen. The rotary tool was held for a predetermined time in such a state that the tip of the rotary tool was positioned at a height of 3.0 mm from the bottom surface of the recess, after which the rotary tool was drawn up, to finish the friction stir welding.
By the above-mentioned procedure, the surface treatment portion of about 3.0 mm in thickness was formed in the recess of the specimen. Next, a surface layer of the surface treatment portion was removed by 0.1 mm by turning process, thereby planarizing the upper surface of the disk-shaped specimen. Note that while burs of the specimen base material were formed in the periphery of the recess due to the pressing-in of the rotary tool, the burs were removed by the turning process.
By variously changing the materials of the powder 51 and the powder 52, a plurality of kinds of surface treatment portions were formed in the recesses of the specimens, as Examples 1-1 to 1-8. The materials of the powder 51 and the powder 52 and the materials of the rotary tool in Examples 1-1 to 1-8 are as set forth in
As the metallic powder, a powder produced by an atomizing method was used. In
The material of the rotary tool to be used in the friction stir welding method is preferably selected according to the kind of the metallic material contained in the material to be joined. In the case where the metallic material is Al or Zn which has a comparatively low melting point, a rotary tool formed from tool steel SKD61 can be used.
In the case where the metallic material is Mg which has high reactivity or Cu which has an intermediate melting point, it is preferable to use a rotary tool formed from a hard metal composed of a WC—Co alloy (a mixed sintered material of tungsten carbide with cobalt). Besides, in the case where the metallic material is Fe, Ti or Ni which has a high melting point, it is preferable to use a rotary tool formed from silicon nitride.
Besides, as seen from
As seen from
Where the metallic powder contained in the powder 51 used as the first-time filling material is aluminum, as in Examples 1-1 and 1-2, the layer formed is joined to the aluminum alloy-made piston base material with a high adhesive strength. However, even where the metallic powder contained in the powder 51 is other metal than aluminum, the layer formed is joined to the aluminum alloy-made piston base material with a sufficient adhesive strength, so long as the metal is a material capable of alloying with aluminum or forming an intermetallic compound with aluminum. For example, magnesium, copper, iron, zinc, titanium, nickel and the like can be used, as in Examples 1-3 to 1-8.
In addition, as seen from
Besides, in the case where the metallic material contained in the powder 51 used in the first-time friction stir welding and the metallic material contained in the powder 52 used in the second-time friction stir welding are of the same kind, a higher adhesion can be obtained at the interface between the first layer and the second layer and at the interface between the second layer and the third layer. While the second layer containing oxygen is formed between the first layer and the third layer, if the metallic materials contained in the first layer and the third layer are of the same kind, a more firmly joined state can be obtained owing to similarity in crystal structure.
In order to confirm the adhesive strength of the surface treatment portion, a tensile adhesion test as specified in JIS-H8402 was conducted. From a specimen, a cylindrical portion with a diameter of 25 mm including the surface treatment portion formed at the surface of the specimen is cut out. Two cylindrical jigs with a diameter of 25 mm are prepared. The two jigs are adhered respectively to an upper surface and a lower surface of the specimen formed with the surface treatment portion, by an epoxy adhesive.
The two cylindrical jigs were pulled by a tensile tester, a tensile stress in a direction perpendicular to the surface treatment portion was thereby generated in the surface treatment portion, and the stress at the time when the surface treatment film was ruptured or peeled off the specimen base material was measured. This stress was evaluated as the adhesive strength of the surface treatment portion. Note that since the breaking strength of the epoxy adhesive is 80 MPa, the epoxy adhesive portion is ruptured in the case where the adhesive strength of the surface treatment portion is equal to or more than 80 MPa. In such a case, the true adhesive strength of the surface treatment portion is not measured, and, therefore, the adhesive strength was evaluated as equal to or more than 80 MPa. When evaluation was conducted for Examples 1-1 to 1-8, the epoxy resin portion was ruptured in all cases. In other words, the adhesive strength was equal to or more than 80 MPa.
Next, by use of the powders 51 and 52 in which the kind of the low-thermal-conductivity material and its content were changed, surface treatment portions were formed on specimens by friction stir welding, to obtain specimens as Examples 1-9 to 1-17. These specimens were also put to evaluation of adhesive strength by the same procedure as above-described for Examples 1-1 to 1-8. Note that in each of these Examples, the same material was used as the powders 51 and 52.
In addition, as comparative examples, Comparative Example 1-1 in which a surface treatment portion was formed using a mixed powder of aluminum and zirconia with a zirconia content in terms of volume ratio of 85% as the powders 51 and 52 and Comparative Example 1-2 in which a surface treatment portion was formed using a mixed powder of aluminum and silica with a silica content in terms of volume ratio of 85% as the powders 51 and 52 were also put to evaluation. The powders 51 and 52 used in production of specimens in Examples 1-9 to 1-17 and Comparative Examples 1-1 and 1-2 and the results of tensile test on the surface treatment portions formed using these materials are set forth in
In the case where the content of the low-thermal-conductivity material in terms of volume ratio was equal to or less than 60%, the epoxy adhesive portion was ruptured, and the adhesive strength was equal to or more than 80 MPa. In the case where the content of the low-thermal-conductivity material in terms of volume ratio was 70%, rupture in the inside of the surface treatment portion (at interface between layers) occurred in Example 1-12 in which the low-thermal-conductivity material was zirconia, whereas the surface treatment portion was ruptured at the interface with the specimen base material occurred in Example 1-16 in which the low-thermal-conductivity material was silica. The adhesive strengths in these Examples were 70 MPa and 65 MPa, respectively. In the case where the content of the low-thermal-conductivity material in terms of volume ratio was 75% (Example 1-13: the low-thermal-conductivity material was zirconia), the adhesive strength was equal to or more than 60 MPa.
In the cases where the content of the low-thermal-conductivity material in terms of volume ratio was 80%, the surface treatment portion was ruptured at the interface with the specimen base material. In Example 1-14 in which the low-thermal-conductivity material was zirconia, the adhesive strength was 18 MPa. Besides, in Example 1-17 in which the low-thermal-conductivity material was silica, the adhesive strength was 21 MPa. In other words, a predetermined adhesive strength was shown in both of these Examples. Note that in the cases where the content of the low-thermal-conductivity material in terms of volume ratio is up to 75%, a high adhesive strength can be obtained, which is more favorable.
Heat insulating characteristic of the surface treatment portion was evaluated. A specific evaluation method will be described referring to
For specimens of Examples and Comparative Examples, the measured values of the peak temperatures T1 and T3 are set forth in the table of
Comparative Example 2-1 is a specimen not having undergone a surface treatment. Comparative Example 2-2 is a specimen in which a single layer of Al-55% ZrO2 with a thickness of 2.9 mm was formed, not by friction stir welding. Comparative Example 2-3 is a specimen in which an alumina layer with a thickness of 20 μm was provided on a surface of the specimen by anodizing. Comparative Example 2-4 is a specimen in which a zirconia layer with a thickness of 1.5 mm was provided on a surface of the specimen by plasma spraying. Note that as every one of the materials of the specimens in these Examples and Comparative Examples, an aluminum alloy (4032-T6) similar to the piston base material was used.
For evaluation of heat insulating characteristic, it is necessary to take a combustion reaction in the internal combustion engine into consideration. This point will be described below. For promoting the combustion reaction in the internal combustion engine, it is important to elevate the surface temperature of the piston crown surface. For example, the autoignition points of light oil and heavy oil are 250° C. to 350° C., and the temperature at the time of ignition of gasoline is about 300° C. For promoting the combustion of these fuels, therefore, it is necessary to raise the surface temperature of the piston crown surface to around 300° C.
In evaluation of heat insulating characteristic in the present embodiment, for realizing an environment inside the combustion chamber of an internal combustion engine on a simulation basis, emission conditions of laser light from the laser light source 64 were so set that the peak temperature upon irradiation of the specimen of Comparative Example 2-1 with the laser light would be about 200° C. Specifically, as shown in
The surface temperature of the specimen rises during when the specimen is irradiated with the laser light, but, when the irradiation with the laser light is stopped, the surface temperature is lowered through natural heat radiation.
A plurality of specimens are irradiated with the laser light from the laser light source 64 as above-mentioned, the temperature variations are measured, and those specimens the surface temperatures of which can be raised to or above 300° C. are evaluated to have an excellent temperature-raising effect.
As seen from
On the other hand, the specimens of Examples 2-1 to 2-8 all showed T3 of equal to or more than 300° C., from which it is seen that these specimens show a sufficient heat insulating effect. In other words, it is seen that the surface treatment portions according to the embodiment of the present invention exhibit a sufficient heat insulating effect.
Particularly, in the specimens of Examples 2-3 to 2-8, the peak temperature T1 upon first-time irradiation with laser is equal to or more than 300° C., and a higher heat insulating effect is observed. This is considered to be because the low-thermal-conductivity material is contained in a volume ratio of equal to or more than 50%, also in the first layer on the surface layer side.
Note that the specimen of Comparative Example 2-4 showed T1 of 510° C., and T3 of 650° C., both being very high temperatures. It is to be noted, however, that the zirconia layer formed by plasma spraying is poor in adhesion at the interface with the specimen base material. In addition, in the case where the heat insulating effect is too high, the temperature rise is excessively localized. For this reason, even if a zirconia coating is formed at the piston crown surface by plasma spraying, durability would be poor, and it would be impossible to obtain a favorable combustion state, so that it is difficult to put the zirconia coating to practical use.
On the other hand, in the cases where the surface treatment portions shown in Examples 2-1 to 2-8 are each applied to the piston crown surface, a heat shielding effect is provided with respect to the depth direction of the surface treatment portion, and moderate heat conduction can be obtained along the surface of the piston crown surface; therefore, a suitable temperature distribution can be obtained through uniform heating of a suitable range, and a sufficient combustion promoting effect can be obtained over a wide range.
A procedure for forming a piston crown surface with a surface treatment portion will be described. Following the flowchart shown in
The joining jig 70 is configured by a base 73, a center jig 71 disposed on an upper surface of the base 73 for supporting a piston 1, and a pair of side jigs 72 movably mounted to the upper surface of the base 73 and fixing the piston 1 from lateral sides. A projection is formed on an upper surface of the center jig 71. In addition, a side surface, on the center jig 71 side, of each of the pair of side jigs 72 is formed as a cylindrical surface equal in radius to the side surface of the piston, and the cylindrical surface is formed with a projection 72a.
At the time of forming a crown surface of the piston 1 with a surface treatment portion by friction stir welding, the piston 1 is fixed as follows. First, a recess in a lower surface of the piston 1 is fitted to a projected portion of the center jig 71, whereby the piston 1 is held on the center jig 1. Next, the pair of side jigs 72 is moved toward the piston 1, the pair of projections 72a is inserted into holes in a side surface of the piston 1, and the side surface of the piston 1 is fixed by pressing from both sides by the cylindrical surfaces of the pair of side jigs 72. By this, the piston 1 is positioned and fixed in a position where a rotary tool is rotated at the time of friction stir welding.
A procedure for forming the surface treatment portion configured as shown in
The piston 1 having a crown surface formed with the surface treatment portion configured in this way was produced following the flow chart shown in
Subsequently, the recess was filled with a powder 51, after which a load was exerted while rotating a rotary tool having a diameter of 30 mm. By this, the powder 51 was pressed in by the rotary tool while crushing the periphery of the recess, to perform first-time friction stir welding, thereby forming the third layer and the second layer in this order. Next, a region over the second layer thus formed was filled with the powder 51, and a load was applied while rotating a rotary tool having a diameter of 32 mm. By this, on the third layer and the second layer previously formed, the third layer and the second layer were further formed in this order by second-time friction stir welding. Similarly, third-time friction stir welding was conducted using a rotary tool having a diameter of 34 mm, whereby the third layer and the second layer in this order were formed alternately and repeatedly three times. Subsequently, a region over the second layer situated at an uppermost portion was filled with a powder 52, and friction stir welding was similarly conducted while rotating a rotary tool having a diameter of 36 mm, whereby the first layer was formed as the uppermost layer. Thereafter, a heat treatment and secondary machining were carried out, to produce the piston 1.
By the above-mentioned steps, in the recess of the piston crown surface for forming the surface treatment portion, there was formed the surface treatment portion configured to have a total of seven layers, where the third layer and the second layer in this order were formed alternately and repeatedly three times and the first layer was formed thereon. The areas of the pluralities of third layers and second layers are so set that an upper layer is larger than a lower layer in diameter, and the first layer is the largest in area. By forming a layer having a thickness of 1 mm by one-time friction stir welding, the surface treatment portion having a thickness of 4 mm in total was formed by four times of friction stir welding. Note that while the diameter of the rotary tool is larger than the diameter of the recess in each run of the above-mentioned friction stir welding, the diameter of the recess and the diameter of the rotary tool may be equal.
The diameter of the rotary tool used for friction stir welding was 30 mm for the first-time friction stir welding, 32 mm for the second-time friction stir welding, 34 mm for the third-time friction stir welding, and 36 mm for the fourth-time friction stir welding. The powder 51 was used as the molding material for the first-time to third-time friction stir welding, and the powder 52 was used as the molding material for the fourth-time friction stir welding.
The layer formed by one-time friction stir welding was 1.0 mm, and the total thickness of the surface treatment portion as a whole was 4.0 mm. An oxygen-containing uppermost layer that was formed at an upper portion of the first layer formed by the fourth-time friction stir welding was cut away by the secondary machining.
By the above-described procedure, the piston 1 as shown in
Note that it has been described above that in the case where a connection portion where the side surface and the bottom surface of the recess for forming the surface treatment portion is not a curved surface, the molding material is left at this portion in the state of not having undergone solid-phase adhesion, thereby causing generation of inadequate solid-phase joining. The reason of this is considered to lie in that heat is liable to be released at the connection portion, and a gap is generated between this portion and the rotary tool at the time of friction stir welding, so that a sufficient load is not easily exerted on the molding material at this portion.
For solving this problem, a method may be contemplated in which the projected portion of the center jig 71 and the recess in a piston lower portion are enhanced in dimensional accuracy, to thereby improve the fitting condition. However, the method in which the above-mentioned connection portion is made to be a curved surface is simpler than the just-mentioned solving method.
As has been described above, according to the present invention, it is possible to provide a piston for an internal combustion engine in which discharge of deposits and smoke is restrained and a favorable fuel cost is obtained owing to excellent heat insulating characteristic. In addition, it is possible to provide a piston for an internal combustion engine that is excellent in durability, since the surface treatment portion and the piston base material are firmly joined to each other.
Note that the present invention is not limited to the above-described embodiments. The specific constituent materials, parts and the like may be modified within such ranges as not to change the gist of the present invention. In addition, addition of known technologies or replacement with known technologies can be made, so long as the constituent elements of the present invention are included.
The disclosure of the following basic application for priority is incorporated herein by reference.
Japanese Patent Application No. 2015-233208 (filed on Nov. 30, 2015)
Number | Date | Country | Kind |
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2015-233208 | Nov 2015 | JP | national |
Filing Document | Filing Date | Country | Kind |
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PCT/JP2016/085433 | 11/29/2016 | WO | 00 |