MACHINE COMPONENT MADE OF FERROUS SINTERED METAL
20210254199 · 2021-08-19
Assignee
Inventors
Cpc classification
F01L2303/01
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F01L1/047
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
B22F3/11
PERFORMING OPERATIONS; TRANSPORTING
B22F1/105
PERFORMING OPERATIONS; TRANSPORTING
C22C33/0257
CHEMISTRY; METALLURGY
B22F5/00
PERFORMING OPERATIONS; TRANSPORTING
F01L1/3442
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F01L2301/00
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F01L2001/34479
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
International classification
B22F1/00
PERFORMING OPERATIONS; TRANSPORTING
B22F3/11
PERFORMING OPERATIONS; TRANSPORTING
B22F5/00
PERFORMING OPERATIONS; TRANSPORTING
F01L1/047
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
Abstract
Raw material powder containing iron powder, copper powder, and tin powder is compressed to form a green compact. The green compact is sintered in a temperature range of from 750 to 900° C., to bond iron structures to each other with copper and tin.
Claims
1-6. (canceled)
7. A method of manufacturing a machine part, the method comprising the steps of: compressing raw material powder containing iron powder, copper powder, and tin powder, to form a green compact; and sintering the green compact in a temperature range of from 750 to 900° C., to bond iron structures to each other with copper and tin.
8. The method of manufacturing of the machine part according to claim 7, wherein the iron structures are bonded to each other with a copper-tin alloy.
9. The method of manufacturing of the machine part according to claim 7, wherein the iron-based sintered metal comprises free graphite.
10. The method of manufacturing of the machine part according to claim 7, wherein the raw material powder comprises 1 to 10 wt % of copper, 0.5 to 2 wt % of tin, and 0.1 to 0.5 wt % of carbon, with the balance being iron.
11. The method of manufacturing of the machine part according to claim 7, wherein the raw material powder has a blending ratio of tin to copper of ⅕ or more and 1 or less in terms of weight ratio.
Description
BRIEF DESCRIPTION OF DRAWINGS
[0013]
[0014]
[0015]
[0016]
[0017]
[0018]
[0019]
[0020]
DESCRIPTION OF EMBODIMENTS
[0021] Now, embodiments of the present invention are described with reference to the drawings.
[0022]
[0023] As illustrated in
[0024] The hydraulic chambers 7 and 8 are each defined with the oil seal 20 in a liquid tight manner. As illustrated in
[0025] As illustrated in
[0026] The oil seal 20 is formed of an iron-based sintered metal. Specifically, the oil seal 20 is formed of an iron-based sintered metal having an iron structure formed mainly of a ferrite phase and having blended therein copper and tin for bonding the iron structures to each other. The iron structures are bonded to each other with a copper-tin alloy. The oil seal 20 according to this embodiment is formed of an iron-based sintered metal containing 1 to 10 wt % (preferably 1 to 8 wt %) of copper, 0.5 to 2 wt % of tin, and 0.1 to 0.5 wt % of carbon, with the balance being iron. The blending ratio of tin to copper is set to ⅕ or more and 1 or less in terms of weight ratio. The iron-based sintered metal contains free graphite. In this embodiment, most of carbon exists as free graphite in the iron-based sintered metal. In the iron-based sintered metal, copper and tin predominantly exist as the copper-tin alloy, and a structure of elemental copper or elemental tin hardly exists. Specifically, the ratio of the elemental copper structure to a copper component in the sintered metal is set to 5 wt % or less, and the ratio of the elemental tin structure to a tin component in the sintered metal is set to 0.1 wt % or less.
[0027] The oil seal 20 is formed by the following procedure: raw material powder obtained by mixing various powders is filled into a mold, followed by being compressed to form a green compact; and the green compact is sintered at relatively low temperature. The raw material powder is mixed powder containing as main components iron powder, copper powder, tin powder, and graphite powder. Various molding aids (a lubricant, a mold release agent, and the like) are added to the mixed powder as required. In this embodiment, there is used raw material powder containing iron powder, copper powder, tin powder, and graphite powder, and having blended therein zinc stearate as a lubricant. The raw material powder and a manufacturing procedure therefor are hereinafter described in detail.
[0028] As the iron powder, any known powder such as reduced iron powder or water-atomized iron powder may be used widely. In this embodiment, the reduced iron powder excellent in oil retaining property is used. The reduced iron powder has a substantially spherical shape as well as an irregular and porous shape. Further, the reduced iron powder has a sponge-like shape with minute projections and depressions provided on its surface, and hence the reduced iron powder is also called sponge iron powder. As the iron powder, there is used iron powder having a grain size of approximately from 40 μm to 150 μm and an apparent density of approximately from 2.0 to 2.8 g/cm.sup.3. The apparent density is defined in conformity to the requirements of JIS Z 8901 (the same applies hereinafter). It should be noted that the oxygen content of the iron powder is set to 0.2 wt % or less.
[0029] As the copper powder, there may widely be used spherical or dendritical copper powder, which is generally used for a sintered metal. For example, electrolytic powder, water-atomized powder, or the like is used. It should be noted that mixed powder of the above-mentioned powders may be used as well. As the copper powder, there is used copper powder having a grain size of approximately from 20 μm to 100 μm and an apparent density of approximately from 2.0 to 3.3 g/cm.sup.3. The copper powder is blended with a view to bonding the iron structures to each other through alloying with tin. In this context, the blending ratio between copper and tin is set so that almost the entire copper powder reacts with tin to form a liquid phase, and thereby penetrates between the iron structures.
[0030] As the tin powder, any known powder such as atomized tin powder is used. For example, there is used tin powder having a grain size of approximately from 10 to 50 μm and an apparent density of approximately from 1.8 to 2.6 g/cm.sup.3. As the graphite powder, any known powder such as flake graphite powder is used. For example, the average grain size and the apparent density are set to approximately from 10 to 20 μm and approximately from 0.2 to 0.3 g/cm.sup.3, respectively.
[0031] The raw material powder obtained by blending the above-mentioned powders includes mixed powder containing 1 to 10 wt % (preferably 1 to 8 wt % of the copper powder, 0.5 to 2 wt % of the tin powder, and 0.1 to 0.5 wt % of the graphite powder, with the balance being the iron powder, and has a trace amount of zinc stearate powder added to the mixed powder. It should be noted that the blending ratio of the tin powder to the copper powder is set to ⅕ or more and 1 or less in terms of weight ratio.
[0032] The raw material powder having the above-mentioned composition is subjected to mixing by means of a known mixer, and then fed to a mold of a molding machine. As illustrated in
[0033] The green compacts 30 are transferred onto a heat-resistant supporting member 60 (for example, a mesh belt) in a non-aligned state in which their directions and postures are not uniformized. Then, the green compacts 30 are sintered in a sintering furnace after being carried therein together with the heat-resistant supporting member 60. The sintering conditions are set so that carbon contained in graphite is prevented from reacting with iron (carbon is prevented from being diffused), and molten tin is brought into contact with copper to form a liquid phase in an alloy state. Specifically, the sintering temperature is set to from 750 to 900° C., preferably from 800 to 850° C. Further, in the conventional manufacturing steps for the sintered metal, endothermic gas (RX gas) obtained through thermal decomposition of a mixture of liquefied petroleum gas (such as butane or propane) and air with a Ni catalyst is often used as a sintering atmosphere. However, in the case of using the endothermic gas (RX gas), the hardening of the surface may occur through the diffusion of carbon. Thus, the sintering atmosphere is set to a gas atmosphere that does not contain carbon (hydrogen gas, nitrogen gas, argon gas, or the like), or to a vacuum. By virtue of those measures, carbon and iron do not react with each other in the raw material powder, and hence a hard structure formed of a pearlite phase γFe (HV 300 or more) is not precipitated. Therefore, the iron structure obtained after the sintering is formed mainly of a relatively soft ferrite phase αFe (HV 200 or less). In this embodiment, almost the entire iron structure (for example, 95 wt % or more of the iron structure) is formed of such ferrite phase. Along with the sintering, zinc stearate blended as a lubricant in the raw material powder is vaporized from inside a sintered compact.
[0034] As described above, the iron-based sintered metal formed mainly of a ferrite phase obtained by the sintering at relatively low temperature has low strength as compared to an iron-based sintered metal formed mainly of a pearlite phase. However, in this embodiment, the bonding strength between the iron structures is increased because the copper powder and the tin powder having high wettability to copper are blended in the raw material powder, and hence liquid phase sintering by the copper-tin alloy progresses. That is, even when the copper powder alone is blended in the raw material powder, the iron structures cannot be bonded to each other because copper does not melt at the above-mentioned sintering temperature. In addition, when the tin powder alone is blended in the raw material powder, the strength is not that increased because tin has low wettability to iron and the bonding force between tin and iron is small, while tin melts at the above-mentioned sintering temperature. Therefore, the copper powder and the tin powder are blended in the raw material powder to allow for progression of the liquid phase sintering. The strength can be ensured at a certain level by copper and tin penetrating between the iron structures and thereby bonding the iron structures to each other.
[0035] In addition, when the sintering is performed at relatively low temperature as described above, deformation such as bending or warpage is less caused by heat during the sintering. Therefore, dimensional accuracy demanded for the oil seal 20 can be obtained without uniformizing the directions and postures of the green compacts during the sintering. Therefore, there is no need to align the plurality of green compacts 30 on the heat-resistant supporting member 60. Thus, the operation is simplified and the risk of damaging the green compacts can be avoided in the alignment operation.
[0036] In addition, when the sintering is performed at relatively low temperature as described above, carbon in graphite is hardly diffused in the iron structure. In particular, in this embodiment, the copper-tin alloy penetrates between the iron structures, and hence carbon in graphite is prevented from being diffused in the iron structure. With such constructions, little graphite is diffused in the iron structure, and almost the entire graphite remains as free graphite. The free graphite is exposed to the entire surfaces of the oil seal 20 including the bottom surface 21.
[0037] Through the above-mentioned sintering step, a porous sintered compact is obtained. Barrel treatment and sizing are carried out on the sintered compact as required, to thereby complete the oil seal 20 illustrated in the figures. As described above, at the time of the sintering, carbon and iron do not react with each other so that the iron structure is formed of the soft ferrite phase. As a result, the sintered compact is likely to flow plastically at the time of the sizing, and hence the sizing can be performed with high accuracy. It should be noted that any one or both of the barrel treatment and the sizing step may be omitted unless otherwise required.
[0038] As illustrated in
[0039] The present invention is not limited to the above-mentioned embodiment. For example, graphite may not be blended in the case where the machine part is not a slide part, which is configured to slide with respect to another member, while the case of blending graphite in the raw material powder for the sintered metal and dispersing the graphite as free graphite in the sintered metal is presented as an example in the above-mentioned embodiment.
[0040] In addition, while the case of applying the present invention to an oil seal for a variable valve timing mechanism is presented in the above-mentioned embodiment, the application of the present invention is not limited thereto. The present invention can be preferably applied to any machine part to be used for an application in which a relatively small load is applied (for example, a bearing or a gear).
REFERENCE SIGNS LIST
[0041] 1 variable valve timing mechanism [0042] 3 rotor [0043] 4 housing [0044] 9 leaf spring [0045] 20 oil seal (machine part) [0046] 30 green compact [0047] 51 die [0048] 52 upper punch [0049] 53 lower punch [0050] 60 heat-resistant supporting member [0051] S cam shaft